THE CASE AGAINST EVOLUTION jrt^^ THE MACMILLAN COMPANY NEW YORK • BOSTOX • CHICAGO • DALLAS ATLANTA • SAN FRANCISCO MACMILLAN & CO.. Limited LONDON • BOMBAY • CALCUTTA MELBOURNE THE MACMILLAN CO. OP CANADAj Lro. TORONTO o / THE CASE AGAINST EVOLUTION BY GEORGE BARRY O'TOOLE, Ph.D., S.T.D. PROFESSOR OF THEOLOGY AND PROFESSOR EMERITUS OF PHILOSOPHY, ST. VINCEXT ARCHABBEY; PROFESSOR OF ANIMAL BIOLOGY, SETON HILL COLLEGE THE MACMILLAN COMPANY 1926 All rights reserved Copyright, 1925, By the macmillan company. Set up and electrotyped. Published April, 1925. Reprinted February, 1926. Printed in the United States of America by J. J. LITTLE AND IVES COMPANY, NEW YORK TO MY MOTHER ADDENDA Note to page 23. — As a result of recent investigations on the sex chromosomes and chromosome numbers in mammals, Theophilus S. Painter reaches the conclusions that polyploidy cannot be invoked to explain evolution within this class. After giving a table of chromosome numbers for 7 out of the 9 eutherian orders, Painter concludes: ''The facts recorded above are of especial interest in that they indicate a unity of chromo- some composition above the marsupial level and effectively dispose of the suggestion that extensive polyploidy may have occurred within this subclass. "In the marsupials the chromosome number is a low one and in the opossum is 22. At first sight it might appear that the eutherian con- dition might have arisen from this by tetraploidy. There are two ob- jections, however. In the first place the bulk of the chromatin in marsupials is about the same as in the eutheria, using the sex chromo- some as our measure. In the second place, polyploidy could scarcely occur successfully in animals with X-Y sex chromosomes, as most mam- mals possess, because of the complication occurring in the sex chromosome balance" (Science, April 17, 1925, p. 424). As the X-Y type of sex chromosomes occurs widely not only among vertebrates, but also among insects, nematodes, and echinoderms. Painter's latter objection excludes evolution by polyploidy from a large portion of the animal kingdom. Note to page 90. — Especially reprehensible, in this respect, are the reconstructions of the Pithecanthropus, the Eoanthropus, and other alleged pitheco-human link modeled by McGregor and others. These imaginative productions, in which cranial fragments are arbitrarily completed and fancifully overlayed with a veneering of human features, have no scientific value or justification. It is consoling, therefore, to note that the great French palaeontologist, Marcelin Boule, in his recent book "Les Hommes Fossiles" (Paris, 1921), has entered a timely protest against the appear- ance of such reconstructions in serious scientific works. "Dubois and Manouvrier," he says, "have given reconstructions of the skull and even of the head (of the Pithecanthropus). These attempts made by medical men, are much too hypothetical, because we do not possess a single element for the reconstruction of the basis of the brain case, or of the jawbones. We are surprised to see that a great palaeontologist, Osbom, publishes efforts of this kind. Dubois proceeded still farther in the realm of imagination when he exhibited at the universal exposi- tion of Paris a plastic and painted reproduction of the Pithecanthropus" (op. cit., p. 105). And elsewhere he remarks: "Some true savants have published portraits, covered with flesh and hair, not only of the Neandertal Man, whose skeleton is known well enough today, but also of the Man of Piltdown, whose remnants are so fragmentary; of the Man of Heidelberg, of whom we have only the lower jawbone; of the Pithecanthropus, of whom there exists only a piece of the cranium and . . . two teeth. Such reproductions may have their place in works of the lowest popularization. But they very much deface the books, though otherwise valuable, into which they are introduced." . . . "Men of science — and of conscience — know the difficulties of such at- tempts too well to regard them as anything more than a pastime" (op. cit., p. 227). Note to page 342. — A fourth possibility is suggested by the case of the so-called skull of the Galley Hill Man, of whose importance as a prehistoric link Sir Arthur Keith held a very high opinion, but which has since turned out to be no skull at all, but merely an odd-shaped piece of stone. CONTENTS PAGE Foreword xi PART I— EVOLUTION IN GENERAL CHAPTER I The Present Crisis in Evolutionary Thought . 1 II Homology and Its Evolutionary Interpretation 31 III Fossil Pedigrees 66 PART II— THE PROBLEM OF ORIGINS I The Origin of Life 131 II The Origin of the Human Soul 189 III The Origin of the Human Body . . . . . 268 Afterword 349 31 5- ^^^ FOREWORD The literature on the subject of evolution has already at- tained such vast dimensions that any attempt to add to it has the appearance of being both superfluous and presumptuous. It is, however, in the fact that the generality of modern works are frankly partisan in their treatment of this theme that the publication of the present work finds justification. For the philosophers and scientists of the day evolution is evidently something which admits of no debate and which must be maintained at all costs. These thinkers are too intent upon making out a plausible case for the theory to take anything more than the mildest interest in the facts opposed to it. If they advert to them at all, it is always to minimize, and never to accentuate, their antagonistic force. For the moment, at any rate, the minds of scientific writers are closed to unfavorable, and open only to favorable, evi- dence, so that one must look elsewhere than in their pages for adequate presentation of the case against evolution. The present work aims at setting forth the side of the question which it is now the fashion to suppress. It refuses to be bound by the convention which prescribes that evolu- tion shall be leniently criticized. It proceeds, in fact, upon the opposite assumption, namely, that a genuinely scientific theory ought not to stand in need of indulgence, but should be able, on the contrary, to endure the acid test of merciless criticism. Evolution has been termed a "necessary hypothesis." We have no quarrel with the phrase, provided it really means evolution as an hypothesis, and not evolution as a dogma. For, obviously, the problem of a gradual differentiation of xi xii FOREWORD organic species cannot even be investigated upon the fixistic assumption, inasmuch as this assumption destroys the prob- lem at the very outset. Unless we assume the possibility, at least, that modern species of plants and animals may have been the product of a gradual process, there is no problem to investigate. It is, however, a far cry from the possibility to the actuality; and the mere fact that an hypothesis is necessary as an incentive to investigation does not by any means imply that the result of the investigation will be the vindication of its inspirational hypothesis. On the contrary, research often results in the overthrow of the very hypothesis which led to its inception. We can, therefore, quite readily admit the necessity of evolution as an hypothesis, while re- jecting its necessity as a dogma. Assent to evolution as a dogma is advocated not only by materialists, who see in evolutionary cosmogony proof posi- tive of their monism and the complete overthrow of the idea of Creation, but also by certain Catholic scientists, who seem to fear that religion may become involved in the anticipated ruin of fixism. Thus all resistance to the theory of evolution is deprecated by Father Wasmann and Canon Dorlodot on the assumption that the ultimate triumph of this theory is inevitable, and that failure to make provision for this even- tuality will lead to just such another blunder as theologians of the sixteenth century made in connection with the Coperni- can theory. Recollection of the Galileo incident is, doubtless, salutary, in so far as it suggests the wisdom of caution and the imperative necessity of close contact with ascertained facts, but a consideration of this sort is no warrant whatever for an uncritical acceptance of what still remains unverified. History testifies that verification followed close upon the heels of the initial proposal of the heliocentric theory, but the whole trend of scientific discovery has been to destroy, rather than to confirm, all definite formulations of the evolu- tional theory, in spite of the immense erudition expended in revising them. FOREWORD xiii There is, in brief, no parity at all between Transformism and the Copernican theory. Among other points of difference, Tuccimei notes especially the following: 'The Copernican system," he remarks, "explains that which is, whereas evolu- tion attempts to explain that which was; it enters, in other words, into the problem of origins, an insoluble problem in the estimation of many illustrious evolutionists, according to whom no experimental verification is possible, given the processes and factors in conjunction with which the theory was proposed. But what is of still greater significance for those who desire to see a parallelism between the two theories is the fact that the Copernican system became, with the dis- coveries of Newton, a demonstrated thesis, scarcely fifty years after the death of Galileo; the theory of evolution, on the other hand, is at the present day no longer able to hold its own even as an hypothesis, so numerous are its incoherencies and the objections to it raised by its own partisans." (*'La Deca- denza di una Teoria," 1908, p. 11.) The prospect, then, of a renewal of the Galileo episode is exceedingly remote. Far more imminent to the writer seems the danger that the well-intentioned rescuers of religion may be obliged to perform a most humiliating volte face, after hav- ing accepted all too hastily a doctrine favored only for the time being in scientific circles. It is, in fact, by no means inconceivable that the scientific world will eventually discard the now prevalent dogma of evolution. In that case those who have seen fit to reconcile religion with evolution will have the questionable pleasure of unreconciling it in response to this reversal of scientific opinion. On the whole, the safest attitude toward evolution is the agnostic one. It commits us to no uncertain position. It does not compromise our intellectual sincerity by requiring us to accept the dogmatism of scientific orthodoxy as a substitute for objective evidence. It precludes the possible embarrass- ment of having to unsay what we formerly said. And last, but not least, it is the attitude of simple truth ; for the truest xiv FOREWORD thing that Science is, or ever will be, able to say concerning the problem of organic origins is that she knows nothing about it. In the present work, we shall endeavor to show that Evolu- tion has long since degenerated into a dogma, which is believed in spite of the facts, and not on account of them. The first three chapters deal with the theory in general, discussing in turn its genetical, morphological, and geological aspects. The last three chapters are devoted to the problem of origins, and treat of the genesis of life, of the human soul, and of the human body, respectively. While this book is in no sense a work of "popular science," I have sought to broaden its scope and interest by combining the scientific with the philosophic viewpoint. Certain portions of the text are unavoidably technical, but there is much, be- sides, that the general reader will be able to follow without difficulty. Students, especially of biology, geology, and ex- perimental psychology, may use it to advantage as supple- mentary reading in connection with their textbooks. I wish to acknowledge herewith my indebtedness to the Editor of the Catholic Educational Review, Rev. George John- son, Ph.D., to whose suggestion and encouragement the incep- tion of this work was largely due. I desire also to express my sincere appreciation of the services rendered in the revision of the manuscript by the Rev. Edward Wenstrup, O.S.B., Professor of Zoology, St. Vincent College, Pennsylvania. BARRY OTOOLE. St. Vincent Archabbey, January 30, 1925. PART I EVOLUTION IN GENERAL [Co - L tiBRARY : I EVOLUTION IN GENERAL CHAPTER I THE PRESENT CRISIS IN EVOLUTIONARY THOUGHT Three prominent men, a scientist, a publicist, and an orator, have recently made pronouncements on the theory of Evolu- tion. The trio, of course, to whom allusion is made, are Bateson, Wells, and Bryan. As a result of their utter- ances, there has been a general reawakening of interest in the problem to which they drew attention. Again and again, in popular as well as scientific publications, men are raising and answering the question: "Is Darwin- ism dead?" Manifold and various are the answers given, but none of them appears to take the form of an unqualified affirmation or negation. Some reply by drawing a distinction between Darwinism, as a synonym for the theory of evolution in general, and Darwinism, in the sense of the particular form of that theory which had Darwin for its author. Modem research, they assure us, has not affected the former, but has necessitated a revision of ideas with respect to the latter. There are other forms of evolution besides Darwinism, and, as a matter of fact, not Darwin, but Lamarck was the orig- inator of the scientific theory of evolution. Others, though imitating the prudence of the first group in their avoidance of a categorical answer, prefer to reply by means of a distinction based upon their interpretation of the realities of the problem rather than upon any mere terminological consideration. 1 2 THE CASE AGAINST EVOLUTION Of the second group, some, like Osborn, distinguish between the law of evolution and the theoretical explanations of this law proposed by individual scientists. The existence of the law itself, they insist, is not open to question; it is only with respect to hypotheses explanatory of the aforesaid law that doubt and disagreement exist. The obvious objection to such a solution is that, if evolution is really a law of nature, it ought to be reducible to some clear-cut mathematical formula comparable to the formulations of the laws of constant, mul- tiple, and reciprocal proportion in chemistry, or of the laws of segregation, assortment, and linkage in genetics. Assuming, then, that it is a genuine law, how is it that to-day no one ventures to formulate this evolutional law in definite and quantitative terms? Others, comprising, perhaps, a majority, prefer to distin- guish between the fact and the causes of evolution. Practi- cally all scientists, they aver, agree in accepting evolution as an established fact; it is only with reference to the agencies of evolution that controversy and uncertainty are permissible. To this contention one may justly reply that, by all the canons of linguistic usage, a fact is an observed or experienced event, and that hitherto no one in the past or present has ever been privileged to witness with his senses even so elemental a phenomenon in the evolutionary process as the actual origin of a new and genuine organic species. If, however, the admis- sion be made that the term "fact" is here used in an untech- nical sense to denote an inferred event postulated for the pur- pose of interpreting certain natural phenomena, then the statement that the majority of modem scientists agree as to the "fact" of evolution may be allowed to stand, with no fur- ther comment than to note that the formidable number and prestige of the advocates fail to intimidate us. Considerations of this sort are wholly irrelevant, for in science no less than in philosophy authority is worth as much as its arguments and no more. The limited knowledge of the facts possessed by the biolo- PRESENT CRISIS IN EVOLUTIONARY THOUGHT 3 gists of the nineteenth century left their imaginations peril- ously unfettered and permitted them to indulge in a veritable orgy of theorizing. Now, however, that the trail blazed by the great Augustinian Abbot, Mendel, has been rediscovered, work of real value is being done with the seed pan, the incu- bator, the microtome, etc., and the wings of irresponsible specu- lation are clipped. Recent advances in this new field of Mendelian genetics have made it possible to subject to critical examination all that formerly went under the name of "ex- perimental evidence" of evolution. Even with respect to the inferential or circumstantial evidence from palaeontology, the enormous deluge of fossils unearthed by the tireless zeal of modern investigators has annihilated, by its sheer complexity, the hasty generalizations and facile simplifications of a generation ago, forcing the adoption of a more critical attitude. Formerly, a graded series of fossil genera sufiSced for the construction of a "palseontological pedi- gree"; now, the worker in this field demands that the chain of descent shall be constructed with species, instead of genera, for links — "Not till we have linked species into lineages, can we group them into genera." (F. A. Bather, Science, Sept. 17, 1920, p. 264.) This remarkable progress in scientific studies has tended to precipitate the crisis in evolutionary thought, which we propose to consider in the present chapter. Before doing so, however, it will be of advantage to formulate a clear statement of the problem at issue. Evolution, or transformism, as it is more properly called, may be defined as the theory which regards the present species of plants and animals as modified descendants of earlier forms of life. Nowadays, therefore, the principal use of the term evolution is to denote the developmental theory of organic species. It is, however, a word of many senses. In the eighteenth century, for example, it was employed in a sense at variance with the present usage, that is, to designate the non-developmental theory of embryological encasement or preformation as opposed to the developmental theory of epi- 4 THE CASE AGAINST EVOLUTION genesis. According to the theory of encasement, the adult organism did not arise by the generation of new parts (epi- genesis), but by a mere "unfolding" {evolutio) of preexistent parts. At present, however, evolution is used as a synonym for transformism, though it has other meanings, besides, being sometimes used to signify the formation of inorganic nature as well as the transformation of organic species. Evolution, in the sense of transformism, is opposed to fixism, the older theory of Linne, according to whom no spe- cific change is possible in plants and animals, all organisms being assumed to have persisted in essential sameness of type from the dawn of organic life down to the present day. The latter theory admits the possibility of environmentally- induced modifications, which are non-germinal and therefore non-inheritable. It also admits the possibility of germinal changes of the varietal, as opposed to the specific, order, but it maintains that all such changes are confined within the limits of the species, and that the boundaries of an organic species are impassable. Transformism, on the contrary, affirms the possibility of specific change, and assumes that the boun- daries of organic species have actually been traversed. What, then, is an organic species? It may be defined as a group of organisms endowed with the hardihood necessary to survive and propagate themselves under natural conditions {i.e. in the wild state) , exhibiting a common inheritable type, differing from one another by no major germinal difference, perfectly interfertile with one another, but sexuully incom- patible with members of an alien specific group, in such wise that they produce hybrids wholly, or partially, sterile, when crossed with organisms outside their own specific group. David Starr Jordan has wisely called attention to the requisite of viability and survival under natural conditions. "A species," he says, "is not merely a form or group of indi- viduals distinguished from other groups by definable features. A complete definition involves longevity. A species is a kind of animal or plant which has run the gauntlet of the ages and PRESENT CRISIS IN EVOLUTIONARY THOUGHT 5 persisted. ... A form is not a species until it has 'stood.' '' (Science, Oct. 20, 1922, p. 448.) Sexaal (gametic) incompatibility as a criterion of specific distinction, presupposes the bisexual or biparental mode of reproduction, namely, syngamy, and is therefore chiefly ap- plicable to the metista, although, if the view tentatively pro- posed by the protozoologist, E. A. Minchin, be correct, it would also be applicable to the protista. According to this view, no protist type is a true species, unless it is maintained by syngamy (i.e. bisexual reproduction) — "Not until syngamy was acquired," says Minchin, "could true species exist among the Protista." ("An Introduction to the Study of the Proto- zoa," p. 141.) To return, however, to the metista, the horse (Equus cabal- liLs) and the ass (Equus asinus) represent two distinct species under a common genus. This is indicated by the fact that the mule, which is the hybrid offspring of their cross, is entirely sterile, producing no offspring whatever, when mated with ass, horse, or mule. Such total sterility, however, is not essen- tial to the proof of specific differentiation; it suffices that the hybrid be less fertile than its parents. As early as 1686, sterility (total or partial) of the hybrid was laid down by John Ray as the fundamental criterion of specific distinction. Hence Bateson complains that Darwinian philosophy fla- grantly "ignored the chief attribute of species first pointed out by John Ray that the product of their crosses is frequently sterile in a greater or lesser degree." (Science, Jan. 20, 1922, p. 58.) Accordingly, the sameness of type required in members of the same species refers rather to the genotype, that is, the sum-total of internal hereditary factors latent in the germ, than to the phenotype, that is, the expressed somatic char- acters, viz. the color, structure, size, weight, and all other perceptible properties, in terms of which a given plant or ani- mal is described. Thus it sometimes happens that two dis- 6 THE CASE AGAINST EVOLUTION tinct specieS; like the pear-tree and the apple-tree, resemble each other more closely, as regards their external or somatic characters, than two varieties belonging to one and the same species. Nevertheless, the pear-tree and the apple-tree are so unlike in their germinal (genetic) composition that they can- not even be crossed. According to all theories of transformism, new species arise through the transformation of old species, and hence evolu- tionists are at one in affirming the occurrence of specific change. When it comes, however, to assigning the agencies or factors, which are supposed to have brought about this transmutation of organic species, there is a wide divergence of opinion. The older systems of transformism, namely, Lamarckism and Darwinism, ascribed the modification of organic species to the operation of the external factors of the environment, while the later school of orthogenesis at- tributed it to the exclusive operation of factors residing within the organism itself. Lamarckism, for example, made the formation of organs a response to external conditions imposed by the environ- ment. The elephant, according to this view, being maladjusted to its environment by reason of its clumsy bulk, developed a trunk by using its nose to compensate for its lack of pliancy and agility. Here the use or function precedes the organ and molds the latter to its need. Darwinism agrees with Lamarckism in making the environment the chief arbiter of modification. Its explanation of the elephant's trunk, how- ever, is negative rather than positive. This animal, it tells us, developed a trunk, because failure to vary in that useful direction would have been penalized by extermination. Wilson presents, in a very graphic manner, the appalling problem which confronts evolutionists who seek to explain the adaptations of organisms by means of environmental fac- tors. Referring, apparently, to Henderson's "Fitness of the Environment," he says: 'Tt has been urged in a recent valu- able work . . . that fitness is a reciprocal relation, involving PRESENT CRISIS IN EVOLUTIONARY THOUGHT 7 the environment no less than the organism. This is both a true and suggestive thought; but does it not leave the natural- ist floundering amid the same old quicksands? The historical problem with which he has to deal must be grappled at closer quarters. He is everywhere confronted with specific devices in the organism that must have arisen long after the condi- tions of environment to which they are adjusted. Animals that live in water are provided with gills. Were this all, we could probably muddle along with the notion that gills are no more than lucky accidents. But we encounter a sticking point in the fact that gills are so often accompanied by a va- riety of ingenious devices, such as reservoirs, tubes, valves, pumps, strainers, scrubbing brushes, and the like, that are obviously tributary to the main function of breathing. Given water, asks the naturalist, how has all this come into existence and been perfected? The question is an inevitable product of our common sense." (Smithson. Inst. Rpt. for 1915, p. 405.) Impressed with the difficulty of accounting for the phenom- ena of organic adaptation by means of the far too general and unspecific influence of the environment,, the orthogenetic school of transformism inaugurated by Nageli, Eimer, and K61- liker repudiated this explanation, and sought to explain or- ganic evolution on the sole basis of internal factors, such as "directive principles," or germinal determinants. According to this conception, the elephant first developed his trunk under the drive of some internal agency, and afterwards sought out an environment in which the newly-developed trunk would be useful. In other words, orthogenesis makes the organ precede the function, and is therefore the exact reverse of Lamarckism. Evolutionists in general, as we have said, regard our present plants and animals as the modified progeny of earlier forms, understanding by "modified" that which is the product of a trans-specific, as distinguished from a varietal or intra-specific, change. To substantiate the claim that changes of specific magnitude have actually taken place, they appeal to two prin- cipal kinds of evidence, namely: (a) empirical evidence based 8 THE CASE AGAINST EVOLUTION on such variations as are now observed to occur among living organisms; (b) inferential evidence, which aposterioristically deduces the common ancestry of allied organic types from their resemblances and their sequence in geological time. Hence, if we omit as negligible certain subsidiary arguments, the whole evidence for organic evolution may be summed up under three heads: (1) the genetic evidence grounded on the facts of variation; (2) the zoological evidence based on homology, that is, on structural resemblance together with all further resemblances (physiological and embryological), which such similarity entails; (3) the palseontological evidence which rests on the gradual approximation of fossil types to modern types, when the former are ranged in a series corresponding to the alleged chronological order of their occurrence in the geological strata. It is the bearing of recent genetical re- search upon the first of these three lines of evidence that we propose to examine in the present chapter, an objective to which a brief and rather eclectic historical survey of evolutionary thought appears to offer the easiest avenue of approach. While many bizarre speculations on the subject of trans- formism had been hazarded in centuries prior to the nineteenth, the history of this conception, as a scientific hypothesis, dates from the publication of Lamarck's "Philosophic Zoologique" in 1809. According to Lamarck, organic species are changed as a result of the indirect influence of the external conditions of life. A change in environment forces a change of habit on the part of the animal. A change in the animal's habits re- sults in adaptation, that is, in the development or suppression of organs through use or disuse. The adaptation, therefore, thus acquired was not directly imposed by the environment, but only indirectly — ^that is, through the mediation of habit. Once acquired by the individual animal, however, the adapta- tion was, so Lamarck thought, taken up by the process of in- heritance and perpetuated by being transmitted to the animal's offspring. The net result would be a progressive differentia- PRESENT CRISIS IN EVOLUTIONARY THOUGHT 9 tion of species due to this indirect influence of a varying en- vironment. Such was the theory of Lamarck, and it is sound and plausible in all respects save one, namely, the unwarranted assumption that acquired adaptations are inheritable, since these, to quote the words of the Harvard zoologist, G. H. Parker, ^'are as a matter of fact just the class of changes in favor of the inheritance of which there is the least evidence." ("Biology and Social Problems," 1914, p. 103.) The next contribution to the philosophy of transformism was made by Charles Darwin, when, in the year 1859, he pub- lished his celebrated ''Origin of Species." In this work, the English naturalist bases the evolution of organic species upon the assumed spontaneous tendency of organisms to vary minutely from their normal type in every possible direction. This spontaneous variability gives rise to slight variations, some of which are advantageous, others disadvantageous to the organism. The enormous fecundity of organisms multiplies them in excess of the available food supply, and more, accord- ingly, are born than can possibly survive. In the ensuing competition or struggle for existence, individuals favorably modified survive and propagate their kind, those unfavorably modified perish without progeny. This process of elimination Darwin termed natural selection. Only individuals favored by it were privileged to propagate their kind, and thus it hap- pened that these minute variations of a useful character were seized upon and perpetuated ''by the strong principle of inheritance.'' In this way, these ^slight but useful modifica- tions would tend gradually to accumulate from generation to generation in the direction favored by "natural selection," until, by the ensuing summation of innumerable minor dif- ferences verging in the same direction, a major difference would be produced. The end-result would be a progressive divergence of posterity from the common ancestral type, whence they originally sprang, ending in a multiplicity of new forms or species, all differing to a greater or lesser extent from 10 THE CASE AGAINST EVOLUTION the primitive type. The contrary hypothesis of a possible convergence of two originally diverse types towards eventual similarity Darwin rejected as an extremely improbable ex- planation of the observed resemblance of organic forms, which, not without reason, he thought it more credible to ascribe to their assumed divergence from a common ancestral type. Such was the scheme of evolution elaborated by Charles Dar- win. His hypothesis leaves the origin of variations an unsolved mystery. It assumes what has never been proved, namely, the efficacy of "natural selection." It rests on what has been definitely disproved by factual evidence, namely, the inherit- ability of the slight variations, now called fluctuations, which, not being transmitted even, by the hereditary process, cannot possibly accumulate from generation to generation, as Darwin imagined. Moreover, fluctuations owe their origin to vari- ability in the external conditions of life {e.g. in temperature, moisture, altitude, exposure, soil, food, etc.), being due to the direct influence or pressure of the environment, and not to any spontaneous tendency within the organism itself. Hence Darwin erred no less with respect to the spontaneity, than with respect to the inheritability and summation, of his "slight variations." The subsequent history of Lamarckian and Darwinian Transformism is briefly told. That both should pass into the discard was inevitable, but, thanks to repeated revisions under- taken by loyal adherents, their demise was somewhat retarded. In vain, however, did the Neo-Darwinians attempt to do for Darwinism what the Neo-Lamarckians had as futilely striven to do for Lamarckism. The revisers succeeded only in pre- cipitating a lethal duel between these two rival systems, which has proved disastrous to both. The controversy begun in 1891 between Herbert Spencer and August Weismann marked the climax of this fatal conflict. Spencer refused to see any value whatever in Darwin's principle of natural selection, while other Neo-Lamarckians, less extreme, were content to relegate it to the status of a sub- PRESENT CRISIS IN EVOLUTIONARY THOUGHT 11 ordinate factor in evolution. Darwin had considered it "the most important means of modification," but it is safe to say that no modern biologist attaches very much importance to natural selection as a means of accounting for the differences which mark off one species from another. In fact, if natural selection has enjoyed, or still continues to enjoy, any vogue at all, it is not due to its value in natural science (which, for all practical intents and purposes, is nil), but solely to its appeal as "mechanistic solution"; for nothing further is needed to commend it to modern thinkers infected with what Wasmann calls Theophobia. Natural selection, in making the organism a product of the concurrence of blind forces unguided by Divine intelligence, a mere fortuitous result, and not the reali- zation of purpose, has furnished the agnostic with a miserable pretext for omitting God from his attempted explanation of the universe. "Here is the knot," exclaims Du Bois-Reymond, "here the great difficulty that tortures the intellect which would understand the world. Whoever does not place all activity wholesale under the sway of Epicurean chance, who- ever gives only his little finger to teleology, will inevitably arrive at Paley's discarded 'Natural Theology,' and so much the more necessarily, the more clearly he thinks and the more independent his judgment. . . . The possibility, ever so dis- tant, of banishing from nature its seeming purpose, and put- ting a blind necessity everywhere in the place of final causes, appears, therefore, as one of the greatest advances in the world of thought, from which a new era will be dated in the treat- ment of these problems. To have.somewhat eased the torture of the intellect which ponders over the world-problem will, as long as philosophical naturalists exist, be Charles Darwin's greatest title to glory." [Darwin versus Galiani, "Reden," Vol. I, p. 211.) But however indispensable the selection principle may be to a philosophy which proposes to banish the Creator from crea- tion, its scientific insolvency has become so painfully apparent that biologists have lost all confidence in its power to solve 12 THE CASE AGAINST EVOLUTION the problem of organic origins. It is recognized, for example, that natural selection would suppress, rather than promote, development, seeing that organs have utility only in the state of perfection and are destitute of selection-value while in the imperfect state of transition. Again, the specific differences that diversify the various types of plants and animals are notoriously deficient in selection-value, and therefore the present differentiation of species cannot be accounted for by means of the principle of natural selection. Finally, unless one is prepared to make the preposterous assumption that the environment is a telic mechanism expressly designed for shap- ing organisms, he is under logical necessity of admitting that the influence of natural selection cannot be anything else than purely destructive. There is, as Wilson points out, no aprior- istic ground for supposing that natural selection could do anything more than maintain the status quo, and as for factual proofs of its effectiveness in a positive sense, they are wholly wanting. Professor Caullery of the Sorbonne, in his Harvard lecture of Feb. 24, 1916, assures us that, "since the time of Darwin, natural selection has remained a purely speculative idea and that no one has been able to show its efficacy in concrete indisputable examples." Considerations of this sort induced not only Neo-Lamarck- ians, but many non-partisans as well, to take the field against the Darwinian Selection Principle. Thus Spencer's caustic at- tack became a forerunner of others, and eminent biologists, like Fleischmann, Driesch, T. H. Morgan, and Bateson, have in turn poured the vials of their satire upon the attempts of Neo-Darwinians to rehabilitate the philosophy of natural selection. Wm. Bateson warns those, who persist in their credulity with reference to the Darwinian account of organic teleology, that they "will be wise henceforth to base this faith frankly on the impregnable rock of superstition and to abstain from direct appeals to natural fact." This admonition forms the conclusion of a scathing criticism of what he styles the "fustian of Victorian philosophy." "In the face of what we PRESENT CRISIS IN EVOLUTIONARY THOUGHT 13 know," it runs, "of the distribution of variability in nature, the scope claimed for natural selection must be greatly re- duced. The doctrine of the survival of the fittest is undenia- ble so long as it is applied to the organism as a whole, but to attempt by this principle to find value in all definiteness of parts and functions, and in the name of science to see fitness everywhere, is mere eighteenth century optimism. Yet it was in its application to the parts, to the details of specific dif- ference, to the spots on the peacock's tail, to the coloring of an orchid flower, and hosts of such examples, that the potency of natural selection was urged with greatest emphasis. Shorn of these pretensions the doctrine of the survival of favored races is a truism, helping scarcely at all to account for the diversity of species. Tolerance plays almost as considerable a part. By these admissions the last shred of that teleological fustian with which Victorian philosophy loved to clothe the theory of evolution is destroyed." {Heredity, "Presidential Address to Brit. Ass'n for Advanc. of Science," Aug. 14, 1914.) Nor is this all. The Darwinian Selection Principle is re- proached with having retarded the progress of science. It is justly accused of having discouraged profound and painstak- ing analysis by putting into currency its shallow and spurious solution of biological problems. "Too often in the past," says Edmund Wilson, "the facile formulas of natural selection have been made use of to carry us lightly over the surface of unsus- pected depths that would have richly repaid serious explora- tion." (Smithson. Inst. Rpt. for 1915, p. 406.) In retaliation for the destructive criticism of natural selec- tion, the Neo-Darwinians have proceeded to pulverize the Lamarckian tenet concerning the inheritability of acquired adaptations. Weismann, having laid down his classic dis- tinction between the soma (comprising the vegetative or tissue cells in contact with the environment) and the germ {i.e. the sequestered reproductive cells or gametes, which are sheltered from environmental vicissitudes) , showed that the Lamarckian assumption that a change in the somatic cells (which con- 14 THE CASE AGAINST EVOLUTION stitute the organism of the individual) is registered in the germ cells (which constitute the vehicle of racial inheritance), is supported neither by a priori probability nor by any facts of observation. Germ cells give rise by division to somatic or tissue cells, but the converse is not true ; for, once a cell has become differentiated and specialized into a tissue cell, it can never again give rise by division to germ cells, but only to other tissue cells of its own kind. Hence the possibility of a change in the tissue being transmitted to the germ has no antecedent probability in its favor. Neither is it grounded on the facts of observation. Bodily mutilations of the parent are not transmitted to the offspring. The child of a blacksmith is not born with a more developed right arm than that of a tailor's child. When the ovaries from a white rabbit are grafted into a black rabbit, whose own ovaries have been previously removed, the latter, if mated to a white male, will produce spotlessly white young. Hence the offspring inherit the characters of the germ track of the white female, whence the ovaries were derived, without being influenced in the least by the pigmented somatic cells of the nurse-body {i.e. the black female), into which the ovaries were grafted. Kam- merer's experiments, in which young salamanders were found to exhibit at birth the coloration, which their parents had acquired through the action of sunlight, fail to convince, be- cause, in this case, the bodies of the parents are not suflSciently impervious to light to preclude its direct action upon the ga- metes while in the reproductive organs of the parents. Hence we cannot be sure but that the coloration of the offspring de- rived from these gametes is due to the direct agency of sun- light rather than to the intermediate influence of the modified somatic cells upon the germ plasm. The same objection holds true of the recent experiments, in which the germ cells have been modified by modifying the interior medium or internal environment by means of anti- bodies and hormones. No one doubts the possibility of influ- encing heredity by a direct modification of the germ cells, espe- PRESENT CRISIS IN EVOLUTIONARY THOUGHT 15 cially when, as is always the case in these experiments, the modification produced is destructive rather than constructive. The experiments, therefore, of Prof. M. F. Guyer of Wisconsin University, in which a germinally-transmitted eye defect was produced by injecting pregnant female rabbits with an anti- lens serum derived from fowls immunized to the crystalline lens of rabbits as antigen, are beside the mark. To demon- strate the Lamarckian thesis one must furnish evidence of a constructive addition to inheritance by means of prior somatic acquisition. The transmission of defects artificially pro- duced is not so much a process of inheritance (transmission of type) as rather one of degeneracy (failure to equate the parental type).^ Commenting on Guyer's suggestion that an organism capable of producing antibodies that are germinally- destructive, may also be able to produce constructive bodies, Prof. Edwin S. Goodrich says: "The real weakness of the theory is that it does not escape from the fundamental objec- tions we have already put forward as fatal to Lamarckism. If an effect has been produced, either the supposed constructive substance was present from the first, as an ordinary internal environmental condition necessary for the normal development of the character, or it must have been introduced from without by the application of a new stimulus. The same objection does not apply to the destructive effect. No one doubts that if a factor could be destroyed by a hot needle or picked out with a fine forceps the effect of the operation would persist throughout subsequent generations." {Science, Dec. 2, 1921, p. 535.) But in demonstrating against the Neo-Lamarckians that somatic modifications unrepresented in the germ plasm could have no significance in the process of racial evolution, Weis- mann had (proved too much. His argument was no less telling * A good definition of degeneracy is that of A. F. Tredgold, who says: "I venture to define degeneracy as 'a retrograde condition of the indi- vidual resulting from a pathological variation of the germ cell.' " (Smithson. Inst. Rpt. for 1918, p. 548.) 16 THE CASE AGAINST EVOLUTION against Darwinism than it was against Lamarckism. Darwin's "individual differences" or "slight variations," now spoken of as fluctuations, were quite as unrepresented and unrecorded in the germ cells as Lamarck's "acquired adaptations." There can be no "summation of individual differences" for the simple reason that fluctuations have no germinal basis and are there- fore uninheritable — "We must bear in mind the fact," says Prof. Edmund Wilson, "that Darwin often failed to dis- tinguish between non-inheritable fluctuations and hereditary mutations of small degree." (Smithson. Inst. Rpt. for 1915, p. 406.) Fluctuations, as we have seen, are due to variability in the environmental conditions, e.g. in access to soil nutrients, etc. As an instance of fluctuational variation the seeds of the ragweed may be cited. Normally these seeds have six spines, but around this average there is considerable fluctua- tion in individual seeds, some having as many as nine spines and others no more than one. Yet the plants reared from nine-spine seeds, even when similarly mated, show no greater tendency to produce nine-spine seeds than do plants reared from one-spine seeds. To meet the difiiculty presented by the non-inheritability of the Lamarckian adaptation and the Darwinian fluctuation, De Vries substituted for them those rare and abruptly- appearing inheritable variations, which he called mutations ^ and regarded as elementary steps in the evolutionary process. This new version of transformism was announced by De Vries in 1901, and more fully explained in his "Die Mutations- Theorie" (Leipzig, 1902-1903). Renner has shown that De Vries' new forms of CEnothera were cases of complex hybridi- zation rather than real mutants, as the forms produced by mutation are now called. Nevertheless, the work of Morgan, Bateson, and others leaves little doubt as to the actual occur- ^ The term mutation had been used long before and in a similar sense by the German palaeontologist Waagen, who employed it to designate the variations of a specific type that succeed one another in successive strata, a thing which rarely occurs. (Cf. Waagen's Die Formenreihe des AmmoTutes suhradiatus, Geognost. palaont. Beitr., Berlin, 1869.) PRESENT CRISIS IN EVOLUTIONARY THOUGHT 17 rence of factorial mutants, while Dr. Albert F. Blakeslee has demonstrated the existence of chromosomal mutants. When unqualified, the term mutant usually denotes the factorial mutant, which arises from a change in one or more of the concatenated genes (hereditary factors) of a single chromo- some (nuclear thread) in the germinal {i.e. gametic) complex. All such changes are called factorial mutations. They are hereditarily transmissible, and affect the somatic characters of the race permanently, although, in rare cases, such as that of the bar-eyed Drosophila mutant, the phenomenon of rever- sion has been observed. The chromosomal mutant, on the contrary, is not due to changes in the single factors or genes, but to duplication of one or more entire chromosomes (linkage- groups) in the gametic complex. Like the factorial mutant, it produces a permanent and heritable modification. The in- crease in nuclear material involved in chromosomal mutation {i.e. duplication) seems to cause a proportionate increase in the cytoplasmic mass of the single somatic cells, which mani- fests itself in the phenotype as giantism. De Vries' (Enothera gigas is a chromosomal mutant illustrative of this phenome- non. Besides the foregoing, there is the pseudomutant pro- duced by the factorial recombination, which results from a crossover, i.e. an exchange of genes or factors between two germinal chromosomes of the same synaptic pair. This recip- rocal transfer of genes from one homologous chromosome to another happens, in a certain percentage of cases, during synap- sis. The percentage can be artificially increased by exposing young female hybrids to special conditions of temperature. If these new mutant forms could be regarded as genuine new species, then the fact that such variations are heritable and come within the range of actual observation, would constitute the long-sought empirical proof of the reality of evolution. Consciously or subconsciously, however, De Vries recognized that this was not the case; for he refers to mutants as ''ele- mentary species," and does not venture to present them as authentic organic species. 18 THE CASE AGAINST EVOLUTION The factorial mutant answers neither the endurance test nor the intersterility test of a genuine species. It would, doubt- less, be going too far to regard all such mutant forms as ex- amples of germinal degeneracy, but it cannot be denied that all of them, when compared to the wild type, are in the direc- tion of unfitness, none of them being viable and prosperous under the severe conditions obtaining in the wild state. Bate- son, who seems to regard all mutant characters as recessive and due to germinal loss, declares: "Even in Drosophila, where hundreds of genetically distinct factors have been iden- tified, very few new dominants, that is to say positive addi- tions, have been seen, and I am assured that none of them are of a class which could be expected to be viable under natural conditions. I understand even that none are certainly viable in the homozygous state." (Toronto Address, Science, Jan. 20, 1922, p. 59.) "Garden or greenhouse products," says D. S. Jordan, "are immensely interesting and instructive, but they throw little light on the origin of species. To call them spe- cies is like calling dress-parade cadets 'soldiers.' I have heard this definition of a soldier, 'one that has stood.' It is easy to trick out a group of boys to look like soldiers, but you can not define them as such until they have 'stood.' " {Science, Oct. 20, 1922.) In a word, factorial mutants, owing, as they do, their survival exclusively to the protection of artificial conditions, could never become the hardy pioneers of new species. Bateson insists that the mutational variation represents a change of loss. "Almost all that we have seen," he says, "are variations in which we recognize that elements have been lost." {Science, Jan. 20, 1922, p. 59.) In his Address to the British Association (1914), he cites numerous examples tend- ing to show that mutant characters are but diminutions or intensifications of characters pre-existent in the wild or normal stock, all of which are explicable as effects of the loss (total or partial) of either positive, or inhibitive (epistatic) heredi- tary factors (genes). One of these instances illustrating the PRESENT CRISIS IN EVOLUTIONARY THOUGHT 19 subtractive nature of the factorial mutation is that of the Primula "Coral King," a salmon-colored mutant, which was suddenly given off by a red variety of Primula called "Crim- son King." Such a mutation is obviously based on the loss of a germinal factor for color. The loss, however, is sometimes partial rather than total, as instanced in the case of the purple- edged Picotee sweet pea, which arose from the wholly purple wild variety by fractionation of the genetic factor for purple pigment. Even where the mutational variation appears to be one of gain, as happens when a positive character appears de novo in the phenotype, or when a dilute parental character is intensified in the offspring, it is, nevertheless, interpretable as a result of germinal loss, the loss, namely, total or partial, of a genetic inhibitor. Such inhibitive genes or factors are known to exist. Bateson has shown, for example, that the whiteness of White Leghorn chickens is due, not to the absence of color-factors, but to the presence of a genetic inhibitor — "The white of White Leghorns," he says, "is not, as white in. nature often is, due to the loss of the color elements, but to the action of something which inhibits their expression." (Ad- dress to the Brit. Ass'n, Smithson. Inst. Rpt. for 1915, p. 368.) Thus the sudden appearance in the offspring of a character not visibly represented in the parents may be due, not to germinal acquisition, but the loss of an inhibitory gene, whose elimina- tion allows the somatic character previously suppressed by it to appear. Hence Bateson concludes: "In spite of seeming perversity, therefore, we have to admit that there is no evo- lutionary change which in the pres^ent state of our knowledge we can positively declare to be not due to loss." {Loc. cit., p. 375.) Another consideration, which disqualifies the factorial mu- tant for the role of a new species, is its failure to pass the test of interspecific sterility. When individuals from two distinct species are crossed, the offspring of the cross is either completely sterile, as instanced in the mule, or at least partially so. But when, for example, the sepia-eyed mutant of the vinegar fly is 20 THE CASE AGAINST EVOLUTION back-crossed with the red-eyed wild type, whence it orig- inally sprang, the product of the cross is a red-eyed hybrid, which is perfectly fertile with other sepia-wild hybrids, with wild flies, and with sepia mutants. This proves that the sepia- eyed mutant has departed, so to speak, only a varietal, and not a specific, distance away from the parent stock. Ordinary or factorial mutation does not, therefore, as De Vries imag- ined, produce new species. These mutants do, indeed, meet the requirement of permanent transmissibility, for their dis- tinctive characters cannot be obliterated by any amount of crossing. Nevertheless, the factorial mutation falls short of being an empirical proof of evolution, because it is a varietal, and not a specific, change. In other words, factorial mutants are new varieties and not new species. Only a heritable change based on germinal acquisition of sufficient magnitude to pro- duce gametic incompatibility between the variant and the parent type would constitute direct evidence of the transmu- tation of species, provided, of course, that the variant were also capable of survival under the natural conditions of the wild state. In his Toronto address of December 28, 1921, Wm. Bateson announced the failure of De Vries' Mutation Theory, when he said: ''But that particular and essential bit of the theory of evolution, which is concerned with the origin and nature of species remains utterly mysterious. We no longer feel as we used to do, that the process of variation, now contempora- neously occurring, is the beginning of a work which needs merely the element of time for its completion; for even time cannot complete that which has not yet begun. The conclusion in which we were brought up that species are a product of a summation of variations ignored the chief attribute of species first pointed out by John Ray that the product of their crosses is frequently sterile in greater or less degree. Huxley, very early in the debate, pointed out this grave defect in the evi- dence, but before breeding researches had been made on a large scale no one felt the objection to be serious. Extended PRESENT CRISIS IN EVOLUTIONARY THOUGHT 21 work might be trusted to supply the deficiency. It has not done so, and the significance of the negative evidence can no longer be denied. . . . "If species have a common origin where did they pick up the ingredients which produce this sexual incompatibility? Al- most certainly it is a variation in which something has been added. We have come to see that variations can very com- monly — I do not say always — be distinguished as positive and negative. . . . Now we have no difficulty in finding evidence of variation by loss, but variations by addition are rarities, even if there are any such which must be so accounted. The variations to which interspecific sterility is due are obviously variations in which something is apparently added to the stock of ingredients. It is one of the common experiences of the breeder that when a hybrid is partially sterile, and from it any fertile offspring can be obtained, the sterility, once lost, disap- pears. This has been the history of many, perhaps most, of our cultivated plants of hybrid origin. "The production of an indubitably sterile hybrid from com- pletely fertile parents which has arisen under critical observa- tion is the event for which we wait. Until this event is wit- nessed, our knowledge of evolution is incomplete in a vital respect. From time to time such an observation is published, but none has yet survived criticism." {Science, Jan. 20, 1922, pp. 58, 59.) But what of the chromosomal mutant? For our knowledge of this type of mutation we are largely indebted to Blakeslee's researches and experiments on the^Jimson weed {Datura stra- monium). According to Blakeslee, chromosomal mutants re- sult from duplication, or from reduction, of the chromosomes, and they are classified as balanced or unbalanced types according as all, or only some, of the chromosomal link- age-groups are similarly doubled or reduced. If only one of the homologous chromosomes of a synaptic pair is doubled, the mutant is termed a triploid form. It is balanced when one homologous chromosome is doubled in every synaptic 22 THE CASE AGAINST EVOLUTION pair, but if one or more chromosomes be added to, or sub- tracted from, this balanced triploid complex, the mutant is termed an unbalanced triploid. When all the chromosomes of the normal diploid complex are uniformly doubled, we have a balanced tetraploid race. The subtraction or addition of one or more chromosomes in the case of a balanced tetraploid complex renders it an unbalanced tetraploid mutant. The retention in somatic cells of the haploid niunber of chromo- somes characteristic of gametes and gametophytes gives a balanced haploid mutant, from which hitherto no unbalanced haploids have been obtained. The normal diploid type and the balanced tetraploid type are said to constitute an even balance, while balanced triploids and haploids constitute an odd balance. The odd balances and all the unbalanced mu- tants are largely sterile. Thus, for example, more than 80% of the pollen of the haploid mutant is bad. "The normal Jimson Weed," says Blakeslee, "is diploid (2n) with a total of 24 chromosomes in somatic cells. In previous papers the finding of tetraploids(4n) with 48 chromosomes and triploids (3n) with 36 was reported, as well as unbalanced mutants with 25 chromosomes represented by the formula (2n+l). The finding of two haploid or In plants, which we are now able to report, adds a new chromosomal type to the balanced series of mutants in Datura. This series now stands: In, 2n, 3n, 4n. Since a series of unbalanced mutants has been obtained from each of the other balanced types by the addition or sub- traction of one or more chromosomes, it is possible that a similar series of unbalanced mutants may be obtainable from our new haploid plants, despite the great unbalance which would thereby result." (Science, June 16, 1923, p. 646.) The haploid mutant, of which Blakeslee speaks, has, of course, 12 unpaired chromosomes in its somatic cells. The balanced triploid is, like the haploid mutant, largely sterile, and is only obtainable by crossing the tetraploid race with the normal diploid plant. Since, then, the product of the cross of the diploid and tetraploid races is sterile, the PRESENT CRISIS IN EVOLUTIONARY THOUGHT 23 tetraplodd race fulfills the sterility test of a distinct species. Whether or not it fulfills the endurance test of survival under natural condition is doubtful, inasmuch as diploid Daturas are about three times as prolific as the tetraploid race. More- over, as Blakeslee himself confessed in a lecture at Woods Hole attended by the present writer in the summer of 1923, the origin of a balanced tetraploid form from the normal diploid type by simultaneous duplication of all the chromo- somes in the diploid complex, is an event that has yet to be witnessed. Nor is any gradual transition from the diploid to the tetraploid race, by way of unbalanced types and tri- ploids, conceivable, seeing that such forms are too sterile to maintain themselves, and are, in fact, incapable of trans- mitting their own type in the absence of artificial interven- tion. There are, it is true, some instances, in which diploid and tetraploid races and species occur together in cultivation and in nature. In certain cases, this tetraploidy is merely apparent, being due to fragmentation of the chromosomes; in other cases, it is really due to chromosomal duplication, giving rise to genuine tetraploid forms. The question is often hard to decide, the mere number of the chromosomes being not, in itself, a safe criterion. Of the actual origin, however, of tetraploid from diploid races we have as yet no observational evidence. Hence Blakeslee's researches on the chromosomal mutant have so far failed to furnish experimental proof of the origin of a genuine new species. Besides, waiving all other considerations, the limits within which chromosomal duplica- tion is possible are of necessity sd narrow, that, at best, this phenomenon can only be invoked to explain a very small range of variation. In fact, it is doubtful whether haploidy, triploidy, and tetraploidy have any important bearing what- ever upon the problem of the origin of species. (See Addenda.) The mutation, then, in so far as we have experimental knowledge of it, does not fulfill requirements of a specific change. It cannot even be regarded as an elementary step in the direction of such a change. With this admission, De- 24 THE CASE AGAINST EVOLUTION Vriesianism becomes obsolete, descending like its predecessors, Lamarckism and Darwinism, into the charnel-house of dis- carded systems whose value is historic, but no longer scien- tific. When we enquire into the reason of this common demise of all the classic systems of transformism, we find it to reside in the progress of the new science of Mendelian genetics, whose foundations were laid by an Augustinian monk of the nineteenth century. Six years after the appear- ance of Darwin's ''Origin of Species," Gregor Johann Mendel published a short paper entitled ''Versuche iiber Pflanzen- hybriden," which, unnoticed at the time by a scientific world preoccupied with Darwinian fantasies, was destined, on its coming to light at the beginning of the present century, to administer the final coup de grace to all the elaborate schemes of evolution that had preceded or followed its initial publica- tion. It took half a century, however, before the dust of Dar- winian sensationalism subsided sufliciently, to permit the "re- discovery" of Mendel's solid and genuine contribution to bio- logical science. But the Pralat of the abbey at Briinn never lived to see the day of his triumph. The true genius of his i century, he died unhonored and unsung, a pretender being ' crowned in his stead. For Coulter says of Darwin: "He died ^ / April 19, 1882, probably the most honored scientific man in ) the world." (Evoludm, 1916, p. 35.) Within the small dimensions of the paper, of which we have spoken, Mendel had compressed the results of years of carefully conceived and accurately executed experimentation reduced to precise statistical form and interpreted with a pene- trating sagacity of the highest order. It is no exaggeration to say that his discovery has revolutionized the science of biology, giving it, for the first time, mathematical formulas comparable to those of chemistry. His two laws of in- heritance, namely, the law of segregation and the law of in- dependent assortment of characters, have, as previously inti- mated, become the basis of the new science of Genetics. His analysis of biparental reproduction has interpreted for us the PRESENT CRISIS IN EVOLUTIONARY THOUGHT 25 cytological phenomena of synapsis, meiosis, and syngamy, has explained for us the instability of hybrids, has placed Weismann's speculations concerning the autonomy and con- tinuity of the germ, plasm on a firm basis of experimental fact, has clarified all our notions respecting the mode and range of hereditary transmission, and has, in a word, opened our eyes to that new and hitherto unexplored realm of nature which Bateson calls ''the world of gametes." Efforts have been made to construct systems of transform- ism along Mendelian lines, but none of them has met with notable success. Lotsy, for example, sought to explain all variation on the basis of the rearrangement of preexistent genetic factors brought about by crossing. But such a solution of the problem is very unsatisfactory. In the first place, the generality of hybrid (heterozygous) forms are ruled out on the score of instability. The phenotype of hybrids is directly dependent, not on the genes themselves, but on the diploid com- bination of genes contained in the zygote. This combination, however, is always dissolved in the process of gamete-forma- tion, by the segregative reduction division which occurs in the reproductive organs of the hybrid. Hybrids, therefore, do not breec? trv£, if propagated by sexual reproduction. To maintain constancy of type in hybrids, one must resort to somatogenic reproduction {i.e. vegetative growth from stems, etc.). Certain violets, in fact, as well as blackberries, are maintained in a state of constant hybridism by means of this sort of reproduc- tion, even in nature. In the case of balanced lethals {i.e. fac- tors causing death in the pure Qr homozygous state), the hybrid phenotype may be maintained even by sexual re- production, inasmuch as all the pure (homozygous) off- spring are non-viable. Two lethals are said to be balanced, when they occur, the first in one and the second in the other homologous chromosome of the same synaptic pair. "Such a factorial situation would maintain a state of constant heterozygosis, the fixed hybridism of an impure species . . . the hybrid will breed true until the relative position of the 26 THE CASE AGAINST EVOLUTION lethals are changed by a crossover, or the genetical constitu- tion in these respects is altered by a mutation." (Davis, Science, Feb. 3, 1922, p. 111.) As is evident, however, the condition of balanced lethals involves a considerable reduc- tion in fertility. Hybridization, moreover, is successful between varieties of the same species rather than between distinct species. Inter- specific crosses are in some cases entirely unproductive, in other cases productive of wholly-sterile, hybrids, and in still other cases productive of semisterile hybrids. When semi- sterile hybrids are obtainable from an interspecific cross, the phenotype can be kept constant by somatogenic reproduction, but, as we shall see in a later chapter, this kind of reproduction does not counteract senescence, and stock thus propagated usually plays out within a determinate period. Finally, the mixture of incompatible germinal elements involved in an interspecific cross tends to produce forms, which are subnormal in their viability and vitality. The conclusions of Goodspeed and Clausen are the following: "(1) As a consequence of modern Mendelian developments, the Mendelian factors may be considered as making up a reaction system, the elements of which exhibit more or less specific relations to one another ; (2) strictly Mendelian results are to be expected only when the contrast is between factor differences within a common Mendelian reaction system as is ordinarily the case in varie- tal hybrids; (3) when distinct reaction systems are involved, as in species crosses, the phenomena must be viewed in the light of a contrast between systems rather than between spe- cific factor differences, and the results will depend upon the degree of mutual compatibility displayed between the specific elements of the two systems." (Amer. Nat., 51 (1917), p. 99.) To these conclusions may be added the pertinent observation of Bradley Moore Davis: "Of particular import," he says, "is the expectation that lethals most frequently owe their presence to the heterozygous condition since the mixing of diverse germ plasms seems likely to lead to the breaking down of delicate PRESENT CRISIS IN EVOLUTIONARY THOUGHT 27 and vital adjustments in proportion relative to the degree of protoplasmic confusion, and this means chemical and phys- ical disturbance." {Science, Feb. 3, 1923, p. 111.) But crossing produces, in the second filial generation (F2), pure (homozygous) as well as hybrid (heterozygous) forms. In some cases these pure forms are new, the phenotype being different from that of either pure grandparent. Such a result is produced by random assortment of the chromosomes in gamete and zygote formation, and occurs when the genes for two or more pairs of contrasted characters are located in dif- ferent chromosome pairs. The phenomenon is formulated in Mendel's Second Law, the law of independent assortment. The novelty, however, of the true-breeding forms thus produced is not absolute, but relative. There is no origination of new hereditary factors. It is simply a recombination of the old genes of different stocks, the genes themselves undergoing no intrinsic alteration. The combination is new, but not the elements combined. In addition to chromosomal recombina- tion, we have factorial recombination by means of crossovers. This, too, can produce new and true-breeding forms of a fixed nature, but here, likewise, it is the combination, and not the elements combined, which is new. The "new" forms thus pro- duced are called, as we have seen, pseudomutants. When pseudomutations, that is, crossovers, occur in conjunction with the condition of balanced lethals, they closely simulate gen- uine factorial mutations. This is exemplified in the case of De Vries' (Enothera Lamarchiana, which is the product of a crossover supervening upon a situation of balanced lethals. In cases of this kind, the crossover releases hitherto suppressed recessive characters, giving the appearance of real mutation. "The workers with Drosophila," says Davis, "seem inclined to believe that much of the phenomena simulating mutation in their material is in reality the appearance of characters set free by the breaking of lethal adjustments which held the characters latent. Well-known workers have arrived at simi- lar conclusions for (Enothera material and are not content to 28 THE CASE AGAINST EVOLUTION accept as evidence of mutations the behavior of Lamarckiana and some other forms when they throw their marked vari- ants." (Science, Feb. 3, 1922, p. 111.) The new forms, however, resulting from random assortment and crossovers cannot be regarded as new species. "Analysis," says Bateson, ''has revealed hosts of transferable characters. Their combinations sufiice to supply in abundance series of types which might pass for new species, and certainly would be so classed if they were met with in nature. Yet critically tested, we find that they are not distinct species and we have no reason to suppose any accumulation of characters of the same order would culminate in the production of distinct species. Specific difference therefore must be regarded as probably attaching to the base upon which these transfer- ables are implanted, of which we know absolutely nothing at all. Nothing that we have witnessed in the contemporary world can colorably be interpreted as providing the sort of evidence required." {Science, Jan. 20, 1922, pp. 59, 60.) Anyone thoroughly acquainted with the results of genetical analysis and research will find it impossible to escape the conviction that there is no such thing as experimental evi- dence for evolution. In spite of the enormous advances made in the fields of genetics and cytology, the problem of the origin of species is, scientifically speaking, as mysterious as ever. No variation of which we have experience is interpre- table as the transmutation of a specific type, and David Starr Jordan voices an inevitable conclusion when he says: ''None of the created 'new species' of plant or animal I know of would last five years in the open, nor is there the slightest evidence that any new species of field or forest or ocean ever originated from mutation, discontinuous variation, or hybridi- zation." {Science, Oct. 20, 1922, p. 448.) "In any case," as Professor Caullery tells us in his Harvard lecture on the "Problem of Evolution," "we do not see in the facts emerging from Mendelism, how evolution, in the sense that morphology suggests, can have come about. And it PRESENT CRISIS IN EVOLUTIONARY THOUGHT 29 comes to pass that some of the biologists of greatest authority in the study of Mendelian heredity are led, with regard to evolutiun, either to a more or less complete agnosticism, or to the expression of ideas quite opposed to those of the preceding generation; ideas which would almost take us back to crea- tionism." (Smithson. Inst. Rpt. for 1916, p. 334.) It is, of course, impossible within the limits of a single chapter to convey any adequate impression of all that Mendel's epoch- making achievement portends, but what has been said is sufficient to give some idea of the acuteness of the crisis through which the theory of organic evolution is passing as a result of his discovery. In its classic forms of Lamarckism, Darwinism and De-Vriesianism, the survival of the theory is out of the question. Whether or not it can be rehabilitated in any form whatever is a matter open to doubt. Transfixed by the innumerable spears of modern objections, its extrem- ity calls to mind the plight of the Lion of Lucerne. Possibly, it is destined to find a rescuer in some great genius of the future, but of one thing, at least, we may be perfectly certain, namely, that, even if rejuvenated, it will never again resume the lineaments traced by Charles Darwin. In the face of this certainty, it is almost pitiful to hear the die-hards of Dar- winism bolstering up a lost cause with the wretched quibble that, though natural selection has been discredited as an ex- planation of the differentiation of species, Darwinism "in its essentials" survives intact. For, if there is any feature which, beyond all else, deserves to be called an essential of Darwin's system, surely it is natural selection. For Darwin it was "the most important" agency of transformation (cf. "Origin of Species," 6th ed., p. 5) . Apart from his hypothesis of the sum- mation through inheritance of slight variations ("fluctua- tions"), now completely demolished by the new science of genetics, it represented his sole contribution to the philosophy of transformism. It alone distinguishes Darwinism from La- marckism, its prototype. Without it the "Origin of Species" would be Hamlet without the Prince of Denmark. With it 30 THE CASE AGAINST EVOLUTION Darwin's fame should stand or fall. Therefore, since Darwin erred in making it "the most important means of modifica- ion," Darwinism is dead, and no grief of mourners can re- suscitate the corpse. "Through the last fifty years," says Bateson, "this theme of the natural selection of favored races has been developed and expounded in writings innumerable. Favored races certainly can replace others. The argument is sound, but we are doubtful of its value. For us that debate stands adjourned. We go to Darwin for his incomparable collection of facts. We would fain emulate his scholarship, his width, and his power of exposition, but to us he speaks no more with philosophical authority. We read his scheme of evolution as we would those of Lucretius or of Lamarck, de- lighting in their simplicity and their courage." (Heredity, Presid. Add. to British Assoc, for Advanc. of Science, Smith. Inst. Rpt. for 1915, p. 365.) CHAPTER II HOMOLOGY AND ITS EVOLUTIONARY INTERPRETATION The recent revival of interest in the problem of evolution seems to have called forth two very opposite expressions of opinion from those who profess to represent Catholic thought on this subject. M. Henri de Dorlodot, in his *'Le Dar- winisme," appears in the role of an ardent admirer of Darwin and an enthusiastic advocate of the doctrine of Transformism. The contrary attitude is adopted by Mr. Alfred McCann, whose *'God — or Gorilla" is bitterly antagonistic not only to Dar- winism but to any form whatever of the theory of Trans- formism. Both of these works possess merits which it would be unjust to overlook. Dorlodot deserves credit for having shown conclusively that there is absolutely nothing in the Scriptures, or in Patristic tradition, or in Catholic theology, or in the philosophy of the Schools, which conflicts with our acceptance of organic evolution as an hypothesis explanatory of certain biological facts. In like manner, it must be acknowledged that, even after a liberal discount has been made in penalty of its bias and scientific inaccuracy, Mr. McCann's book still con- tains a formidable residue of serious objections, which the friends of evolution will probably find it more convenient to sidestep than to answer. Unfortunately, however, neither of these writers maintains that balanced mental poise which one likes to see in the defenders of Catholic truth. Dorlodot seems too profoundly impressed with the desirability of occupying a popular posi- tion to do impartial justice to the problem at issue, and his anxiety to keep in step with the majority blinds him apparently 31 32 THE CASE AGAINST EVOLUTION to the flaws of that "Darwinism" which he praises. Had he been content with a simple demarcation of negative limits, there would be no ground for complaint. But, when he goes so far as to bestow unmerited praise upon the author of the mechanistic "Origin of Species" and the materialistic "Descent of Man"; when, by confounding Darwinism with evolution, he consents to that historical injustice which allows Darwin to play Jacob to Lamarck's Esau, and which leaves the original genius of Mendel in obscurity while it accords the limelight of fame to the unoriginal expounder of a borrowed conception; when, by means of the sophistry of anachronism, he speciously endeavors to bring the speculations of an Augustine or an Aquinas into alignment with those of the ex-divinity student of Cambridge; when he assumes that Fixism is so evi- dently wrong that its claims are unworthy of consideration, whereas Transformism is so evidently right that we can dis- pense with the formality of examining its credentials; when, in a word, he expresses himself not merely in the sense, but in the very stereotyped cant phrases of a dead philosophy, we realize, with regret, that his conclusions are based, not on any reasoned analysis of the evidence, but solely upon the dogma- tism of scientific orthodoxy, that his thought is cast in anti- quated molds, and that for him, apparently, the sixty-five years of discovery and disillusionment, which have intervened since the publication of the "Origin of Species," have passed in vain. But, if Dorlodot represents the extreme of uncritical ap- proval, Mr. McCann represents the opposite, and no less repre- hensible, extreme of biased antagonism, that is neither fair in method nor conciliatory in tone. Instead of adhering to the time-honored practice of Catholic controversialists, which is rather to overstate than to understate the argument of an ad- versary, Mr. McCann tends, at times, to minimize, in his restatement, the force of an opponent's reasoning. He fre- quently belittles with mere flippant sneer, and is only too ready to question the good faith of those who do not share his con- HOMOLOGY AND ITS INTERPRETATION 33 victions. Thus, when McCann ridicules Wells and accuses him of pure romancing, because the latter speaks of certain hairy "wild women" of the Caves, he himself seems to be ignorant of the fact that a palaeolithic etching has been found repre- senting a woman so covered with hair that she had no need of other apparel (the bas-relief from Laugerie-Basse carved on reindeer palm — cf. Smithson. Inst. Rpt. for 1909, p. 540 and Plate 2). Mr. McCann may object, with truth, that this is far from being a proof that the primitive representatives of the human race were hairy individuals, but the fact suffices, at least, to acquit Mr. Wells of the charge of unscrupulous invention. Hence, while we have no wish to excuse the lamentable lack of scientific conscientiousness so manifestly apparent in the writings of popularizers of evolution, like Wells, Osborn, and Haeckel, nevertheless common justice, not to speak of charity, constrains us to presume that, occasionally at least, their de- partures from the norm of objective fact were due to ordinary human fallibility or to the mental blindness induced by pre- conceptions, rather than to any deliberate intent to deceive. And we feel ourselves impelled to make this allowance for unconscious inaccuracy all the more readily that we are con- fronted with the necessity of extending the selfsame indulgence to Mr. McCann himself. Thus we find that the seventh illus- tration in ''God — or Gorilla" (opposite p. 56) bears the legend: "Skeletons of man and chimpanzee compared," when, in point of fact, the ape skeleton in question is not that of a chimpanzee {Troglodytes niger) at all, but of an Orang-utan {Simla satyms), as the reader may verify for himself by consulting Plate VI of the English version of Wasmann's "Modern Biology," where the identical illustration appears above its proper title: "Skeleton of an adult Orang-utan." Since the error is repeated in the index of illustrations and in the legend of the third illustration of the appendix, it is impossible, in this instance, to shift the responsibility from Mr. McCann to the printer. In any case, it is sincerely to be hoped that this. 34 THE CASE AGAINST EVOLUTION and several other infelicitous errors will be rectified in the next edition of "God — or Gorilla." In the next chapter we shall have occasion to refer again to Dorlodot's book. For the present, however, his work need not concern us, while in that of Mr. McCann we single out but one point as germane to our subject, namely, the latter's inade- quate rebuttal of the evolutionary argument from homology. The futility of his method, which consists in matching insigni- ficant differences against preponderant resemblances, and in exclaiming with ironic incredulity: ''Note extraordinary resem- blances!" becomes painfully evident, so soon as proper pre- sentation enables us to appreciate the true force of the argu- ment he is striving to refute. Functionally the foot of a Troglodyte ape may be a "hand," but structurally it is the homologue of the human foot, and not of the human hand ; nor is this homology effectually disposed of by stressing the dis- similarity of the hallux, whilst one remains discreetly reticent concerning the similarity of the calcaneum. For two reasons, therefore, the irrelevance of Mr. McCann's reply is of special interest here: (1) because it illustrates concretely the danger of rendering a refutation inconsequential and inept by failing to plumb the full depth of the difficulty one is seeking to solve ; (2) because it shows that it is vain to attempt to remove man's body from the scope of this argument by citing the in- considerable structural differences which distinguish him from the ape, so that, unless the argument from homology proves upon closer scrutiny to be inherently inconclusive, its applica- bility to the human body is a foregone conclusion, and implies with irresistible logic the common ancestry of men and apes. Such are the reflections suggested by the meager measure of justice which Mr. McCann accords to the strongest zoological evidence in favor of evolution, and they contain in germ a feasible program for the present chapter, which, accordingly, will address itself: first, to the task of ascertaining the true significance of homology in the abstract as well as the full extent of its application in the concrete; second, to that of HOMOLOGY AND ITS INTERPRETATION 35 determining with critical precision its intrinsic value as an argument for the theory of transmutation. Homology is a technical term used by the systematists of botany, zoology and comparative anatomy to signify basic structural similarity as distinguished from superficial func- tional similarity, the latter being termed analogy. Organisms are said to exemplify the phenomenon of homology when, be- neath a certain amount of external diversity, they possess in common a group of correlated internal resemblances of such a nature that the organisms possessing them appear to be con- structed upon the same fundamental plan. In cases of this kind, the basic similarity is frequently masked by a veneer of unlikeness, and it is only below this shallow surface of diver- gence that we find evidences of the identical structure or com- mon type. Thus organs of different animals are said to be homologous when they are composed of like parts arranged in similar rela- tion to one another. Homologous organs correspond bone for bone and tissue for tissue, so that each component of the one finds its respective counterpart in the other. The organs in question may be functionally specialized and externally differ- entiated for quite different purposes, but the superficial diver- sity serves only to emphasize, by contrast, the underlying identity of structure which persists intact beneath it. Thus, for example, the wing of a pigeon, the flipper of a whale, the foreleg of a cat, and the arm of a man are organs differing widely in function as well as outward appearance, but they are called homologous, none the less, because they all exhibit the same basic plan, being composed of similar bones similarly disposed with respect to one another. Organs, on the other hand, are called analogous which, though fundamentally unlike in structure, are, nevertheless, superficially modified and specialized for one and the same function. The wing of a bird and the wing of an insect furnish a trite instance of such analogy. Functionally they subserve the same purpose, but structurally they bear no relation to 36 THE CASE AGAINST EVOLUTION each other. In like manner, though both are devoted to the same function, there exists between the leg of a man and the leg of a spider a fundamental disparity in structure. At times, specialization for the selfsame function involves the emergence of a similar modification or uniform structural adaptation from a substrate of basic dissimilarity. In these instances of parallel modifications appearing on the surface of divergent types, we have something more than mere func- tional resemblance. Structure is likewise involved, albeit superficially, in the modification which brings about this exter- nal uniformity. In such cases, analogy is spoken of as con- vergence, a phenomenon of which the mole and the mole-cricket constitute a typical example. The burrowing legs of the insect are, so far as outward appearance goes, the exact replica on a smaller scale of those of the mole, though, fundamentally, their structure is quite unlike, the mole being built on the endoskeletal plan of the vertebrates, whereas the mole-cricket is constructed on the exoskeletal plan characteristic of the arthropods. Speaking of the first pair of legs of the mole- cricket, Thomas Hunt Morgan says: "By their use the mole- cricket makes a burrow near the surface of the ground, similar to, but of course much smaller than, that made by the mole. In both of these cases the adaptation is the more obvious, be- cause, while the leg of the mole is formed on the same general plan as that of other vertebrates, and the leg of the mole- cricket has the same fundamental structure as that of other in- sects, yet in both cases the details of structure and the general proportions have been so altered that the leg is fitted for en- tirely different purposes from those to which the legs of other vertebrates and other insects are put." (Quoted by Dwight in "Thoughts of a Catholic Anatomist," p. 235.) In the analogies of convergence, therefore, we have the exact converse of the phenomenon so often encountered in connection with homology. The latter exhibits a contrast between basic identity and super- ficial diversity, the former a contrast between superficial con- vergence and fundamental divergence. HOMOLOGY AND ITS INTERPRETATION 37 Now the extreme importance of homology is manifest from the fact that the taxonomists of zoology and botany have found it to bb the most satisfactory basis for a scientific classification of animals and plants. In both of these sciences, organisms are arranged in groups according as they possess in common certain points of resemblance whereby they may be referred to this, or that, general type. The resemblance is most com- plete between members of the same species, which do not differ from one another by any major difference, though they may exhibit certain minor differences justifying their sub- division into varieties or races. These morphological consid- erations, however, must, in the case of an organic species, be supplemented by the additional physiological criteria of perfect sexual compatibility and normal viability, as we have already had occasion to note in the previous chapter. When organisms, though distinguished from one another by some major difference, agree, notwithstanding, in the main elements of structure, the several species to which they belong are grouped under a common genus, and similarly genera are grouped into families. A relative major difference, such as a difference in the size of the teeth, suffices for the segregation of a new species, while an absolute difference, such as a differ- ence in the number of teeth or the possession of an additional organ, suffices for the segregation of a new genus. In practice, however, the classifications of systematists are often very arbi- trary, and we find the latter divided into two factions, the "lumpers" who wish to reduce the number of systematic groups and the "splitters" who have a passion for breaking up larger groups into smaller ones on the basis of tenuous differences. Above the families are the orders, and they, in turn, are as- sembled in still larger groups called classes, until finally we reach the phyla or branches, which are the supreme categories into which the plant and animal kingdoms are divided. As we ascend the scale of classification, the points of resemblance be- tween the organisms classified are constantly decreasing in number, while the points of difference increase apace. Hence, 38 THE CASE AGAINST EVOLUTION whereas members of the same species have very much in com- mon, members of the same phylum have very little in common, and members of different phyla show such structural disparity that further correlation on the basis of similarities becomes impossible (in the sense, at least, of a reliable and consistent scheme of classification), all efforts to relate the primary phyla to one another in a satisfactory manner having proved abortive. Within the confines of each phylum, however, homology is the basic principle of classification. But the scientist is not content to note the bare fact of its existence. He seeks an ex- planation, he wishes to know the raison d'etre of homology. Innumerable threads of similarity run through the woof of divergence, and the question arises: How can we account for the coexistence of this woof of diversity with a warp of simi- larity? Certainly, if called upon to explain the similarity ex- istent between members of one and the same species, even the man in the street would resort instinctively to the principle of inheritance and the assumption of common ancestry, exclaim- ing: "Like sire, like son!" It is a notorious fact that children resemble their parents, and since members of the same species are sexually compatible and perfectly interfertile, there is no difficulty whatever in the way of accepting the presumption of descent from common ancestral stock as a satisfactory solution of the problem of specific resemblance. Now, it is precisely this selfsame principle of heredity which the Transformist invokes to account for generic, no less than for specific, similarity. In fact, he presses it further still, and professes to see therein the explanation of the resemblances observed between members of the different families, orders, and classes, which systematists group under a common phylum. This, of course, amounts to a bold extension of the principle of inheritance far beyond the barriers of interspecific sterility to remote applications that exceed all possibility of experimental verification. Transform- ists answer this difficulty, however, by contending that the period, during which the human race has existed, has been, HOMOLOGY AND ITS INTERPRETATION 39 geologically speaking, all too brief, and characterized by envi- ronmental conditions much too uniform, to afford us a favor- able opportunity for ascertaining the extreme limits to which the genetic process may possibly extend; and, even apart from this consideration, they say, racial development (phylogeny) may be, like embryological development (ontogeny) an irre- versible process, in which case no recurrence whatever of its past phenomena are to be expected in our times. Be that as it may, the evolutionist interprets the resem- blances of homology as surviving vestiges of an ancient ances- tral type, which have managed to persist in the descendants notwithstanding the transformations wrought in the latter by the process of progressive divergence. Moreover, just as the existence of a common ancestor is inferred from the fact of resemblance, so the relative position in time of the common ancestor is inferred from the degree of resemblance. The common ancestor of forms closely allied is assumed to have been proximate, that of forms but distantly resembling each other is thought to have been remote. Thus the common an- cestor of species grouped under the same genus is supposed to have been less remote than the common ancestor of all the genera grouped under one family. The same reasoning is ap- plied, mutatis mutandis, to the ancestry of families, orders and classes. The logic of such inferences may be questioned, but there is no blinking the fact that, in practice, the genetic explanation of homology is assumed by scientists to be the only reasonable one possible. In fact, so strong is their confidence in the neces- sity of admitting a solution of this kind, that they do not hesitate to make it part and parcel of the definition of homol- ogy itself. For instance, on page 130 of Woodruff's "Founda- tions of Biology" (1922) , we are informed that homology signi- fies "a fundamental similarity of structure based on descent from a common antecedent form." The Yale professor, how- ever, has been outdone in this respect by Professor Calkins of Columbia, who discards the anatomical definition altogether 40 THE CASE AGAINST EVOLUTION and substitutes, in lieu thereof, its evolutionary interpretation. ''When organs have the same ancestry," he says, "that is, when they come from some common part of an ancestral type, they are said to be homologous." ("Biology," p. 165.) In short, F. A. Bather is using a consecrated formula culled from the modern biological creed when he says: "The old form of diagnosis was yer genus et differ entiam. The new form is per proavum et modificationemJ' {Science, Sept. 17, 1920, p. 259.) A moment's reflection, however, will make it clear that, in thus confounding the definition proper with its theoretical in- terpretation, the modern biologist is guilty of a logical atrocity. Homology, after all, is a simple anatomical fact, which can be quite adequately defined in terms of observation; nor is the definition improved in the least by having its factual elements diluted with explanatory theory. On the contrary, the defini- tioi is decidedly weakened by such redundancy. And as for those who insist on defining homology in terms of atavistic assumption instead of structural affinity, their procedure is tantamount to defining the clear by means of the obscure, an actual effect by means of a possible cause. Moreover, this attempt to load the dice in favor of Transformism by tamper- ing with the definition of homology ends by defeating its own purpose. For, if homology is to serve as a legitimate argu- ment for evolution, then obviously evolution must not be included in its definition; otherwise, the conclusion is antici- pated in the premise, the question is begged, and the argument itself rendered a vicious circle. Having formed a sufficiently clear conception of homology as a static fact, we are now in a position to consider the prob- lem of its causality with reference to the solution proposed by evolutionists. Transmutation, they tell us, results from the interaction of a twofold process, namely, the conservative and similifying process called inheritance, and progressive and diversifying process known as variation. Inheritance by trans- mitting the ancestral likeness tends to bring about uniform- HOMOLOGY AND ITS INTERPRETATION 41 ity. Variation by diverting old currents into new channels adjust organisms to new situations and brings about modifica- tion. Homology, therefore, is the effect of inheritance, while adaptedness or modification is the product of variation. As here used, the term inheritance denotes something more than a mere recurrence of parental characters in the off- spring. It signifies a process of genuine transmission from generation to generation. Strictly speaking, it is not the char- acters, such as coloration, shape, size, chemical composition, structural type, and functional specificity, that are ''inherited," but rather the hereditary factors or chromosomal genes, which are actually transmitted, and of which the characters are but an external expression or manifestation. Hence, it is scarcely accurate to speak of "inherited," as distinguished from ''ac- quired," characters. As a matter of fact, all somatic charac- ters are joint products of the interaction of germinal and environmental factors. Consequently, the external char- acter would be affected no less by a change in the envi- ronmental factors than by a change in the germinal factors. In a word, somatic characters are not the exclusive expression of the genetic factors, but are equally dependent upon environ- mental influence, and hence it is only to the extent that these characters are indicative of the specific constitution of the germ plasm that we may speak of them as "inherited," remem- bering that what is really transmitted to the offspring is a complex of genes or germinal factors, and not the characters themselves. The sense is, therefore, that "inherited" char- acters are manifestative of what is contained in the germ plasm, whereas "acquired" characters have no specific germ- inal basis, but are a resultant of the interaction between the somatic cells and the environment. In modern termin- ology, as we have seen, the aggregate of germinal factors transmitted in the process of reproduction is called the genotype, while the aggregate of somatic characters which manifest these germinal factors externally is spoken of as the phenotype. Only the genotype is transmitted, the phenotype 42 THE CASE AGAINST EVOLUTION being the subsequent product of the interplay of genetic fac- tors and environmental stimuli, dependent upon, and expres- sive of, both. Variation, therefore, may be based upon a change in the germ plasm, or in the environment, or in both. If it rests exclusively upon an extraordinary change in the environ- mental conditions, the resulting modification is non-inherit- able, and will disappear so soon as the exceptional environ- mental stimulus that evoked it is withdrawn. If, on the contrary, it is based upon a germinal change, it will manifest itself, even under ordinary, i.e. unchanged or uniform envi- ronmental influence. In this case, the modification is inherit- able in the sense that it is the specific effect of a transmissible germinal factor, which has undergone alteration. As we have seen in the foregoing chapter, there are three kinds of germinal change which result in "inheritable" modifications. The first is called factorial mutation, and is initiated by an alteration occurring in one or more of the chromosomal genes. The second is called chromosomal mutation, and is caused by duplication (or reduction) of the chromosomes. The third may be termed recombination, one type of which results from the crossover or exchange of genes between pairing chromo- somes ("pseudomutation"), the other from random assortment in accordance with the Mendelian law of the independence of allelomorphic pairs. This so-called 'Random assortment of the chromosomes" is the result of the shuffling and free deals of the chromosomal cards of heredity which take place twice in the life-cycle of organisms: viz. first, in the process of gametic reduction (meiosis) ; second, in the chance meeting of vari- ously-constituted sperms and eggs in fertilization. A mis- chance of the first of these "free deals" is bewailed in the following snatch from a parody belonging to the Woods Hole anthology. "Oh chromosomes, my chromosomes, How sad is my condition! My grandsire's gift for writing well HOMOLOGY AND ITS INTERPRETATION 43 Has gone to some lost polar cell And so I write this doggerel, I cannot do much better." These kinds of variation, however, in so far as they fall within the range of actual observation, are confined within the limits of the organic species. Intra-specific variation, however, will not suflace. To account for the adaptive modi- fications superimposed upon underlying structural identity, Transformism is obliged to assume the possibility of trans- specific variation. Yet in none of the foregoing processes of variation do we find a valid factual basis for this assumption. Factorial mutation, for instance, waiving its failure to produce naturally-viable forms, or to meet the physiological sterility test of a new species, admits of interpretation as a change of loss due to the "dropping out" of a gene from the germinal complex. Bateson's conception of evolution as a process consisting in the gradual loss of inhibitive genes, whose elimination releases suppressed potentialities, seems rather incredible. Many will be inclined to see in Castle's facetious epigram a reductio ad absurdum of Bateson's sug- gestion; for, according to the latter's view, as the Harvard professor remarks, we should have to regard man as a simplified amceba. Certainly, it seems nothing short of a contradiction to ascribe the progressive complication of the phenotype to a simplification of the genotype by loss. On the other hand, not only is there no experimental evi- dence of a germinal change by positive acquisition, that is, by the addition of genes, but it is hard to conceive how such a change could come about. "At first," admits Bateson, "it may seem rank absurdity to suppose that the primordial form or forms of protoplasm could have contained complexity enough to produce the divers types of life." "But," he asks, "is it easier to imagine that these powers could have been conveyed by extrinsic addition? Of what nature could these additions be? Additions of material can not surely be in question. We are told that salts of iron in the soil may turn 44 THE CASE AGAINST EVOLUTION a pink hydrangea blue. The iron cannot be passed on to the next generation. How can iron multiply itself? The power to assimilate iron is all that can be transmitted. A disease- producing organism like the pebrine of silkworms can in a very few cases be passed on through the germ cells. But it does not become part of the invaded host, and we can not conceive it taking part in the geometrically ordered processes of segregation. These illustrations may seem too gross; but what refinement will meet the requirements of the problem, that the thing introduced must be, as the living organism itself is, capable of multiplication and of subordinating itself in a definite system of segregation?" (Heredity, Smithson. Inst. Rpt. for 1915, p. 373.) Nor can we agree with Prof. T. H. Morgan's contention that the foregoing difficulty of Bateson has been solved by the discovery of the chromosomal mutation. All unbalanced chromosomal mutants are subnormal in their viability and vitality, not to speak of their marked sterility. Haploidy represents a regressive, rather than a progressive, step. The triploid mutant is sterile. The tetraploid race of Daturas is inferior in fertility to the normal diploid plant. The origin of balanced tetraploidy from diploidy must be presumed, since it has never been observed. Moreover, tetraploidy represents only quantitative, and not qualitative, progress. The increased mass of the nucleus produces an enlargement of the cytoplasm, the result of which is giantism. This effect, however, is not specific; for giant and normal races possessing each the same number of chromosomes are known to exist in nature. Hence giantism may be due to other causes besides chromosomal duplication. The only effect of this doubling is a reinforcement and intensification of the former effect of the genetic factors, their specificity remaining unchanged. Double doses are sub- stituted for single doses of the factors, but nothing really new is added. Morgan himself recognizes that this mere repeti- tion of identical genes is insufficient, and that their multipli- cation must be qualitative as well as numerical, to answer HOMOLOGY AND ITS INTERPRETATION 45 the specifications of a progressive step in evolution. Hence he suggests that the chromosomal mutation is subsequently sup- plemented by appropriate factorial mutation. Once this sup- position is made, however, all the objections we have mentioned in connection with factorial mutation [e.g the subnormality of its products, its intra-specific nature, etc.) return to plague the speculator, and, in addition to these, he is confronted with the new difficulty of explaining how the redundance of duplicate genes can be removed and replaced by coordinate differentiation in their respective specificities. Now we have no factual evidence whatever of such a solidaric re- differentiation of the germinal factors, that would modify harmoniously the composition and role of each and every gene in the factorial complex. Nor is there any possibility whatever of accounting for this telic superregulation of the germinal regulators upon a purely mechanistic basis. How can the ultimate chemical determinants of heredity be thus redetermined? Consequently, although there is gametic in- compatibility between diploid races and the tetraploid races, which are said to have arisen from the former, we are not, nevertheless, warranted, by what has been experimentally verified, in regarding tetraploid races as new species, or as progressive steps in the process of organic evolution. To conclude, therefore, we have experimental verification of the efficacy of the similifying process said to have been at work in evolution, namely, inheritance. The same, however, cannot be said of the correlative diversifying process of trans- specific variation, which is said to have superficially modified old structures into new species. The latter process, accord- ingly, is but a pure postulate of science known to us only through the effect hypothetically assigned to it, namely, the adaptive modification. The adaptation, however, of which there is question here is not to be confounded with the *^ acquired adaptation" of Lamarckian fame; for, unlike the latter, it is an inheritable modification rooted in the germ plasm. Adaptations of this 46 THE CASE AGAINST EVOLUTION sort do, indeed, adjust the organism to its external environ- ment, but they are innate and not acquired. Hence they are often spoken of as preadaptations; for they precede, in a sense, the organism's contact with the environing element to which they adjust it. They may possibly, it is true, have been acquired in the distant past, but they have now a specific germinal foundation, and no one was ever privileged to wit- ness their initial production de novo. The whale, for example, though fundamentally a warm-blooded mammal, is super- ficially a fish, by reason of such a preadaptation to its marine environment. Preadaptation is of common occurrence, espe- cially among parasites, symbiotes, commensals, and inquilines. Wasmann cites innumerable instances of beetles and flies so profoundly modified, in accommodation to their mode of life as guests in termite nests, that the systematist hesitates to classify them under any of the accepted orders of insects. Here the adaptive modification so disturbs the underlying homology as to make of these creatures taxonomical ambigui- ties. In the case of Termitomyia, he tells us, "the whole de- velopment of the individual has been so modified that it resembles that of a viviparous mammal rather than that of a fly." ("The Problem of Evolution," pp. 14, 15.) Such modifications, however, amount to major, and not merely minor, differences. We are not dealing, therefore, with varietal distinctions here, but with specific, generic, and even ordinal differences. With reference to the phenomenon of adap- tive modification,^ three things, consequently, are worthy of note: (1) it has the semblance of being adventitious to the un- * It may be remarked, in passing, that experimental genetics and mutation furnish no clue to the origin of adaptive characters. The Lamarckian idea alone gives promise in this direction. Orthogenesis leaves unsolved the mystery of preadaptation; yet only orthogenetic systems of evolution can be constructed on the basis of genetical facts. "Mutations and Mendelism," says Kellogg, "may explain the origin of new species in some measure, but they do not explain adaptation in the slightest degree." {Atlantic Monthly, April, 1924, pp. 488, 489.) We have seen in the previous chapter that they are impotent to ex- plain in any measure the origin of new species. HOMOLOGY AND ITS INTERPRETATION 47 derlying structural uniformity; (2) it is of such magnitude that it cannot be ascribed to variation within the species; (3) it has been appropriated by the hereditary process, in the sense that it is now an "inherited" character based on the trans- mission of specific germinal factors. Now it is claimed that for the occurrence of this kind of modification in conjunction with homology only one rational explanation is possible, and that explanation is evolution. If this contention be a sound one, and Dorlodot, who claims certitude for the evolutionary solution, insists that it is such, then, in the name of sheer logical consistency, but one course lies open to us. We cannot stop at Wasmann's comma,^ we must press on to the very end of the evolutionary sentence and sing with the choristers of Woods Hole: "It's a long way from Amphioxus, It's a long way to us; It's a long way from Amphioxus, To the meanest human cuss. Good-bye fins and gill slits; Welcome skin and hair. It's a long, long way from Amphioxus, But we came from there." In this predicament it will not do, as we shall see presently, to adopt Mr. McCann's expedient of balancing anatomical dif- ferences against anatomical resemblances. To do so is to court certain and ignominious defeat. We must, therefore, examine the argument dispassionately. If it be solid, we must accept it and give it general application. If it be unsound, we must detect its flaws and expose them. Intellectual hon- esty allows us no alternative! Moreover, in weighing the argument from organic homology we must not lose sight of the two important considerations previously stressed: (1) that the inference of common an- 'Rev. Erich Wasmann, S. J., accepts the evolutionary inference from homology as regards plants and animals. When it comes to man, how- ever, he attempts to draw the line, and argues painstakingly against the assumption of a bestial origin of the human body. 48 THE CASE AGAINST EVOLUTION cestry in the case of homologous forms is based, not upon this or that particular likeness, but upon an entire group of coor- dinated resemblances; (2) that the resemblances involved are not exterior similarities, but deep-seated structural uniformi- ties perfectly compatible with diversities of a superficial and functional character. "Nothing," says Dr. W. W. Keen, "could be more unlike externally than the flipper of a whale and the arm of a man. Yet you find in the flipper the shoulderblade, humerus, radius, ulna, and a hand with the bones of four fingers masked in a mitten of skin." (Science, June 9, 1922, p. 605.) In fact, the resemblances may, in certain instances, be so deeply submerged that they no longer appear in the adult organism at all and are only in evidence during a transitory phase of the embryological process. In such cases, the embryo or larva exhibits, at a particular stage, traces of a uniformity completely obliterated from the adult form. In short, though frequently presented as a distinct argument, embryological similarity, together with all else of value that can still be salvaged from the wreck of the Mliller-Haeckel Law of Em- bryonic Recapitulation, is, at bottom, identical with the gen- eral evolutionary argument from homology. In the latter argument we are directed to look beneath the modified surface of the adult organism for surviving vestiges of the ancestral type. In the former, we are bidden to go deeper still, to the extent, that is, of descending into the very embryological process itself, in order to discover lingering traces of the an- cestral likeness, which, though now utterly deleted from the transformed adult, are yet partially persistent in certain embryonic phases. In sectioning a larval specimen of the fly-like termite-guest known as Termitoxenia Heimi, Father Wasmann came across a typical exemplification of this embryological atavism. In the adult insect, a pair of oar-like appendages replace the wings characteristic of the Diptera (flies) . These appendages are organs of exudation, which elaborate a secretion whereof HOMOLOGY AND ITS INTERPRETATION 49 the termites are very fond, and thereby render their possessors welcome guests in the nests of their hosts. The appendages, therefore, though now undoubtedly inherited characters, are the specific means by which these inquilines are adapted to their peculiar environment and mode of life among the ter- mites. Moreover, the organs in question not only differ from wings functionally, but, in the adult, they bear no structural resemblance whatever to the wings of flies. Nevertheless, on examining his sections of the above-mentioned specimen, Was- mann found a developmental stage of brief duration during which wing veins appeared in the posterior branches of the embryonic appendages. Now, assuming that Wasmann's technique was faultless, his specimen normal, and his interpre- tation correct, it is rather difficult to avoid his conclusion that we have here, in this transitory larval phase, the last sur- viving vestige of ancestral wings now wholly obliterated from the adult type, that, consequently, this wingless termite guest is genetically related to the winged Diptera, and that we must see in the appendages aboriginal wings diverted from their primitive function and respecialized for the quite different pur- pose of serving as organs of exudation, (cf. "Modern Biology," p. 385.) Indeed, phenomena of this kind seem to admit of no other explanation than the atavistic one. It should be remembered, however, that Wasmann does not appear to have verified the observation in more than one specimen, and that a larger number of representative specimens would have to be accurately sectioned, strained, examined and interpreted, before any reliable conclusion could be drawn.^ Such, in its most general aspect, is the atavistic solution of the problem presented by the homology of types. In it, ^This transitory lymphatic, or tracheal venation appearing in the appendages at the stenogastric stage may not have the particular significance that Father Wasmann assigns. Such venation, even if vestigial and aborted, need not necessarily be a vestige of former toing venation. To demonstrate the validity of the atavistic inter- pretation, ail other possible interpretations would have to be defi- nitively excluded. 50 THE CASE AGAINST EVOLUTION similarity and diversity are harmoniously reconciled, in the sense that they affect, respectively, different structural, or different developmental, levels. It is futile, therefore, to look for contradictions where they do not exist. In a word, the attempt to create opposition between a group of basic and correlated uniformities, on the one hand, and some particular external difference, on the other, is not only abortive, but absolutely irrelevant as well. The reason is obvious. Only when likeness is associated with unlikeness is it an argument for Transmutation. Likeness alone would demonstrate Immu- tability by indicating a process of pure inheritance as dis- tinguished from the process of variation. Hence evolutionists do not merely concede the coexistence of diversity with simi- larity, they gladly welcome this fact as vitally necessary to their contention. Now it is precisely this point which Mr. McCann, like many other critics of evolution, fails utterly to apprehend. Con- sequently, his efforts to extricate the human foot from the toils of simian homology are entirely unavailing. To offset the force of the argument in question, it is by no means sufficient, as he apparently imagines, to point to the fact that, unlike the hallux of the ape, the great toe in man is non- opposable (cf. "God — or Gorilla," pp. 183, 184, and legends under cuts opposite pp. 184 and 318). The evolutionist will reply at once that the non-opposability of man's great toe is cor- related with the specialization of the human foot for progres- sion only, as distinguished from prehension; while, in the ape, whose foot has retained both the progressive and the prehensile function, the hallux is naturally opposable in adaptation to the animal's arboreal habits. He will then call attention to the undeniable fact that, despite these adaptational differences, the bones in the foot of a Troglodyte ape are, bone for bone, the counterparts of the bones in the human foot and not of those in the human hand. He will readily concede, that, so far as function and adaptedness go, this simian foot is a "hand," but he will not fail to point out that it is, at the HOMOLOGY AND ITS INTERPRETATION 51 same time, a heeled hand equipped with a calcaneum, a talus, a navicular, a cuboid, and all other structural elements requi- site to ally it to the human foot and distinguish it from the human hand. In fact, Mr. McCann's own photographs of the gorilla skeleton show these features quite distinctly, though he himself, for some reason or other, fails to speak of them. It is to be feared, however, that his adversaries may not take a charitable view of his reticence concerning the simian heel, but may be inclined to characterize his silence as "discreet," all the more so, that he himself has uncomplimentarily credited them with similar discretions in their treatment of unmanageable facts. In short, Mr. McCann's case against homology resem- bles the Homeric hero, Achilles, in being vulnerable at the "heel." At all events, the homology itself is an undeniable fact, and it is vain to tilt against this fact in the name of adaptational adjustments like "opposability" and "nonoppos- ability." Since, therefore, our author has failed to prove that this feature is too radical to be classed as an adaptive modi- fication, our only hope of exempting the human skeleton from the application of the argument in question is to show that argument itself is inconsequential. Mr. McCann's predicament resembles that of the un- lucky disputant, who having allowed a questionable major to pass unchallenged, strives to retrieve his mistake by picking flaws in a flawless minor. As Dwight has well said of the human body, "it differs in degree only from that of apes and monkeys," and "if we compare the individual bones with those of apes we cannot fail to see the correspond- ence." ("Thoughts of a Catholic' Anatomist," p. 149.) In short, there exists no valid anatomical consideration whatever to justify us in subtracting the human frame from the exten- sion of the general conclusion deduced from homology. Who- soever, therefore, sees in the homology of organic forms conclusive evidence of descent from a common ancestor, can- not, without grave inconsistency, reject the doctrine of the bestial origin of man. He may still, it is true, exclude the 52 THE CASE AGAINST EVOLUTION human mind or soul from the evolutionary accoimt of origins, but, if homology is, in any sense, a sound argument for com- mon descent, the evolutionary origin of the human body is a foregone conclusion, and none of the anatomical "differences in degree" will avail to spare us the humiliation of sharing with the ape a common family-tree. It remains for us, then, to reexamine the argument critically for the purpose of deter- mining as precisely as possible its adequacy as a genuine demonstration. To begin with, it must be frankly acknowledged that here the theory of transformism is, to all appearances, upon very strong ground. Its first strategic advantage over the theory of immutability consists in the fact that, unlike the latter, its attitude towards the problem is positive and not negative. When challenged to explain the structural uniformities ob- served in organic Nature, the theory of immutability is mute, because it knows of no second causes or natural agencies ade- quate to account for the facts. It can only account for homology by ascribing the phenomenon exclusively to the unity of the First Cause, and, while this may, of course, be the true and sole explanation, to assume it is tantamount to re- moving the problem altogether from the province of natural science. Hence it is not to be wondered at that scientists prefer the theory of transformism, which by assigning inter- mediate causes between the First Cause and the ultimate effects, vindicates the problem of organic origins for nat- ural science, in assuming the phenomena to be proximately explicable by means of natural agencies. Asked whether he believes that God created the now exclusively arboreal Sloth (Bradypus) in a tree, the most uncompromising defender of fixism will hesitate to reply in the affirmative. Yet, in this case, what is nowadays, at least, an inherited preadapta- tion, dedicates the animal irrevocably to tree-life, and makes its survival upon the ground impossible. Analogous preadaptations occur in conjunction with the phenomena of parasitism, symbiosis and commensalism, all of HOMOLOGY AND ITS INTERPRETATION 53 which offer instances of otherwise disparate and unrelated organisnis that are inseparably bound together, in some appar- ently capricious and fortuitous respect, by a preadaptation of the one to the other. Parasites, guests, or symbiotes, as the case may be, they are now indissolubly wedded to some de- terminate species of host by reason of an appropriate and con- genital adjustment. For all that, however, the association seems to be a contingent one, and it appears incredible that the associates were always united, as at present, by bonds of reciprocal advantage, mutual dependence, or one-sided exploi- tation. Yet the basis of the relationship is in each case a now inherited adaptation, which, if it does not represent the primi- tive condition of the race, must at some time have been acquired. For phenomena such as these, orthogenesis, which makes an organ the exclusive product of internal factors, con- ceiving it as a preformed mechanism that subsequently se- lects a suitable function, has no satisfactory explanation. Lamarckism, which asserts the priority of function and makes the environment mold the organ, is equally inacceptable, in that it flouts experience and ignores the now demonstrated existence of internal hereditary factors. But, if between these two extremes some evolutionary via media could be found, one must confess that it would offer the only conceivable "natural explanation" of preadaptation.* All this, of course, is pure speculation, but it serves to show that here, at any rate, the theory of Transformism occupies a position from which it cannot easily be dislodged. But, besides the advantage of being able to offer a "natural explanation" of the association of homology with adaptation, * Vernon Kellogg has expressed this same view in a recent article, though he frankly admits that it is an as yet unrealized desideratum. "Altogether," he says, "it must be fairly confessed that evolutionists would welcome the discovery of the actual possibility and the mechan- ism of transferring into the heredity of organisms such adaptive changes as can be acquired by individuals in their lifetime. It would give them an explanation of evolution, especially of adaptation, much more satisfactory than any other explanation at present claiming the acceptance of biologists." (Atlantic Monthly, April, 1924, p. 488.) 54 THE CASE AGAINST EVOLUTION Transformism enjoys the additional advantage of being able to make the imagination its partisan by means of a visual appeal. Such an appeal is always more potent than that of pure logic stripped of sensuous imagery. When it comes to vividness and persuasiveness, the syllogism is no match for the object-lesson. Retinal impressions have a hypnotic in- fluence that is not readily exorcised by considerations of an abstract order — "Segnius irritant demissa per aurem, Quam quae sunt oculis subjecta fidelibus," says Horace, in the ''Ars Poetica." Philosophers may distinguish between the magnetic appeal of a graphic presentation and the logical cogency of the doctrine so presented, but there is no denying that, in prac- tice, imagination is often mistaken for reason and persuasion for conviction. Be that as it may, the ordinary method of bringing home to the student the evolutionary significance of homology is certainly one that utilizes to the full all the advantages of visual presentation. Given a class of impres- sionable premedics and coeds; given an instructor's table with skeletons of a man, a flamingo, an ape and a dog hierarchically arranged thereon; given an instructor sufiiciently versed in comparative osteology to direct attention to the points in which the skeletons concur: and there can be no doubt whatever as to the psychological result. The student forms spontaneously the notion of a common vertebrate type, and the instructor assures him that this "general type" is not, as it would be with respect to other subject matter, a mere universal idea with no formal existence outside the mind, but rather a venerable family likeness, posed for originally by a single pair of ancestors (or could it possibly have been, by one self-fertilizing hermaphro- dite?) and recopied from generation to generation, with certain variations on the original theme, by the hand of an artist called Heredity. This explanation may be true, but logically con- sequential it is not. However, if the dialectic is poor, the pedagogy is beyond reproach, and the solution proposed has in its favor the fact that it accords well with the student's limited experience. He is aware of the truism that children re- HOMOLOGY AND ITS INTERPRETATION 55 semble their parents. Why look for more recondite explana- tions when one so obvious is at hand? The atavistic theory- gratifies his instinct for simplification, and, if he be of a mechanistic turn of mind, the alternative conception of crea- tionism is quite intolerable. Nevertheless, it goes without saying that the "inference" of common descent from the data of homology is not a ratiocination at all, it is only a simple apprehension, a mere abstraction of similarity from similars — ^'Unde quaecumque inveniuntur convenire in aliqua intentione intellecta," says Aquinas, "voluerunt quod convenirent in una re." {In lib. II sent., dist. 17, q. I, a. 1) Philosophy tells us that the oneness of the universal is conceptual and not at all extramental or real, but the transformist insists that the universal types of Zoology and Botany are endowed with real as well as logical unity, that real unity being the unity of the common ancestor. Certainly, from the standpoint of practical effectiveness, the evolutionary argument leaves little to be desired. The presen- tation is graphic and the solution simple. But for the critic, to whom logical sequence is of more moment than psychologi- cal appeal, this is not enough. To withstand the gnawing tooth of Time and the remorseless probing of corrosive human reason, theories must rest on something sounder than a mirage of visual imagery! Tell me where is fancy bred, Or in the heart or in the head? How begot, how nourished? Reply, reply. It is engendered in the eyes, With gazing fed; and fancy dies In the cradle where it lies. But is it fair thus to characterize the "common ancestors" of Transformism as figments which, like all other abstractions, have no extramental existence apart from the concrete objects whence they were conceived? To be sure, their claim to be real entities cannot be substantiated by direct observation or ex- ^'l' 56 THE CASE AGAINST EVOLUTION periment, and so a factual proof is out of the question. Man> the late-comer, not having been present at the birth of organic forms, can give no reliable testimony regarding their parent- age. In like manner, no a priori proof from the process of inheritance is available, because heredity, as revealed to us by the experimental science of Genetics, can account for specific resemblances only, and cannot be invoked, at present, as an empirically tested explanation for generic, ordinal, or phyletic resemblances. It has still to be demonstrated experimentally that the hereditary process is transcendental to limits imposed by specific differentiation. There remains, however, the a pos- teriori argument, which interprets homology and adaptation as univocal effects ascribable to no other agency than the dual process of inheritance and variation. What are we to think of this argument? Does it generate certainty in the mind, or merely probability? A moment's reflection will bring to light the preliminary flaw of incomplete enumeration of possibilities. To suppose that inheritance alone can account for structural resemblance is an unwarranted assumption. Without a doubt, there are other similifying influences at work in Nature besides inherit- ance. True, inheritance is one possible explanation of the similarity of organisms, but it is not the only one. Even among the chemical elements of inorganic nature we find analogous uniformities or ''family traits," which, in the absence of any reproductive process whatever, we cannot possibly at- tribute to inheritance. Mendeleeff's discovery of the perio- dicity of the elements, arranged in the order of their atomic weights, is well-known. At each interval of an octave, a suc- cession of chemical types, similar to those of the preceding octave, recur. Hence elements appearing in the same vertical column of the Periodic Table have many properties in com- mon and exhibit what may be called a family resemblance. Now, we have in the process of atomic disintegration, as ob- served in radioactive elements and interpreted by the electronic theory of atomic structure, a reasonably satisfactory basis HOMOLOGY AND ITS INTERPRETATION 57 upon which to account for the existence of these inorganic uniformities. Here analogous chemical constitution, produced in accordance with a general law, results in uniformity that implies a similar, rather than an identical, cause. The hy- pothesis of parallelistic derivation from similar independent origins accounts quite as well for the observ^ed uniformities as does the hypothesis of divergent derivation from a single common origin. Why, then, should we lean so heavily on the already overtaxed principle of inheritance, when parallelism is as much a possibility in the organic world as it is an actuality in the inorganic world° As to the contrast here drawn between inheritance and other similifying factors, it is hardly necessary to remark that we are speaking of inheritance as defined in terms of Mendelian experiment and cytological observation. In the so-called chemical theory of inheritance, the distinction would be mean- ingless and the contrast would not exist. Ehrlich's disciple, Adami, sets aside all self-propagating germinal determinants, like the chromomeres, in favor of a hypothetical "biophoric molecule," which is to be conceived as a benzine-like ring bristling with sidechains. Around this determining core the future organism is built up in definite specificity, as an arch is constructed about a template. Adami has merely ap- plied Paul Ehrlich's ideas concerning metabolism and immunity to the question of heredity, commandeering for this purpose the latter's entire toolkit of receptors, haptophores, amboceptors, etc., as though this grotesque paraphernalia of crude and clumsy mechanical symbols (which look for all the world like the wrenches of a machinist, or the lifters used by the cook to remove hot lids from the kitchen range) could throw any valuable light whatsoever on the exceedingly complex, and manifestly vital, phenomenon of inheritance. It does not even deserve to be called a chemical theory, for, as Starling cor- rectly remarks concerning Ehrlich's conception, "though chemi- cal in form," it is not so in reality, because "it does not explain the phenomenon by reference tc the known laws of chemistry." 58 THE CASE AGAINST EVOLUTION (Cf. Physiology, ed. of 1920, p. 1084,) In a word, the theory of heredity, which seeks to strip inheritance of its uniqueness as a vital process by identifying it with the more general phys- icochemical processes occurring in the organism, is a ground- less speculation, that, far from explaining, flouts the very ob- servational data which it pretends to elucidate. Kurz und gut! to requite the mechanist, Schafer, with his own Danielesque phrase, here, as elsewhere, the mechanists have succeeded in extracting from the facts, not what the facts themselves pro- claim, but what preexisted in their own highly-cultured imag- inations so well-stocked with cogs, cranks, ball bearings, and other sesthetic imagery emanating from polytechnic schools and factories. But in arguing from the existence of parallelism in the inorganic world to its possibility in the organic world, we are less liable to displease the mechanists than those other extremists, the neo-vitalists, who will be prone to deny all parity between living, and inanimate, matter. Fortunately, we are in a position to appease the scruples of the latter by referring to the facts of convergence as universally accepted evidence that the phenomenon of parallelism occurs in animate, no less than inanimate, nature. Admitting, therefore, that the laws of organic morphology are of a higher order than those which regulate atomic, molecular, and multimolecular struc- ture, these facts attest, nevertheless, that parallelisms arise in organisms of separate ancestry which are due, not to hered- ity, but to the uniform action of universal morphogenetic forces. Hence general laws can be invoked to account for organic uniformities with the same right that they are invoked to account for resemblances existing between the various members of a chemical "family" like the Halogens. And why should this not be so? Organisms have much in common that transcends any possible scheme of evolution and that cannot be brought into alignment with the position arbi- trarily assigned them in the evolutionary family-tree. They all originate as single cells. Their common means of growth HOMOLOGY AND ITS INTERPRETATION 59 and reproduction is mitotic cell division. This leads to the production of a somatella, among the protista, and of a soma differentiated by histogenesis into two or three primary tissues, among the metista. All these fundamental processes are strikingly uniform throughout the entire plant and animal world. In these universal properties of living matter, there- fore, we have a common basis for general structural and or- ganizational laws, which, though irreducible to the "common ancestors" of Transformism, is quite adequate to account for both the homologies and analogies of living matter. Accept this basis of general laws regulating the development of living matter, and there is no difficulty in seeing why the problems posed by exposure to analogous environmental conditions are solved in parallel fashion by organisms, irrespective of whether they are nearly, or distantly, related in the sense of morphol- ogy. Transformism, on the other hand, can only account for homology at the expense of convergence, and for convergence at the expense of homology. So far as a common ancestral basis is concerned, the two kinds of resemblance are, from the very nature of the case, irreducible phenomena. It is only, in fact, by surrendering the principle that simi- larity entails community of origin, and by falling back on the suggested common basis of general laws, that Transformism makes room in its system for the troublesome facts of con- vergence. "It might be reiterated in passing," says Dwight, "that this 'convergence' business is a very ticklish one. We have been taught almost word for word that resemblance implies relationship, or almost predicates it; but according to this doctrine it has nothing to do with it whatever." ("Thoughts of a Cath. Anat.," p. 190.) And in a subsequent chapter he says: "No very deep knowledge of comparative anatomy is needed for us to know that very similar adapta- tions for particular purposes are found in very diverse animals. The curious low grade mammal, the Ornithorhynchus, with a hairy coat and the bill of a duck, is a familiar instance. We 60 THE CASE AGAINST EVOLUTION all know that the whales have the general form of the fish, al- though they are mammals, and going more into details we know that the whale's flipper is on the same general plan as that of the ancient saurians. . . . The origin of the eye, ac- cording to evolutionary doctrines, has been a very difficult problem, which gets worse rather than better the more you do for it. Even if we could persuade ourselves that certain cells blundered along by the lucky mating of individuals in whom they were a bit better developed than in the others till they came to form a most complicated organ of sight, it would be a sufficient tax on our credulity to believe that this could come off successfully in some extraordinary lucky spe- cies; but that it should have turned out so well with all kinds of vertebrates is really too much to ask us to swallow. But this is not all: eyes are very widely spread among different classes of invertebrates. More wonderful still, the eyes of cer- tain molluscs and Crustacea are on stalks, and this is found also in various and very different families of fishes. How did this happen? Was it by way of descent from the molluscs or the Crustacea? If not, how could chance have brought about such a similar result in diverse forms?" {Op. cit., pp. 233-236.) It may be objected that the resemblances of convergence are superficial analogies, not to be confounded with funda- mental homologies. This contention may be disputed; for, as we shall see in the next chapter, there are cases where the convergence is admittedly radical, and not merely superficial. The distinction, moreover, between shallow and basic char- acters is somewhat arbitrary, and its validity is often ques- tionable. When the skeletal homology that relates the amphibia to the mammals, for instance, is traced to the root of the vertebrate family tree, we find it all but disappearing in a primitive Amphioxus-like chordate, whose so-called skele- ton contains no trace of bone or cartilage. Hence, if we go back far enough, the homologies of to-day become the con- vergences of a geological yesterday, and we find the vertebrate HOMOLOGY AND ITS INTERPRETATION 61 type of skeleton arising independently in reptiles, mammals, amphibia, and fishes. Again, there are times when convergent analogies appear to be more representative of the common racial her- itage than the underlying structure itself, tempting the evolutionist to fly in the face of the orthodox interpretation, which rigidly rules out analogy in favor of homology, and refuses to accept the eloquent testimony of a remark- able resemblance merely because of a slight technical dis- crepancy in the structural substrate. A large pinching claw, or chela, for example, occurs in two organisms belonging to the phylum of the arthropods, namely, the lobster and the African scorpion. Both chelae are practically identical in structure, but, unfortunately, the chela of the lobster arises from a different appendage than that from which the scor- pion's chela emerges. If they arose from corresponding ap- pendages, they would be pronounced "homologous organs" and acclaimed, without hesitation, as strong evidence in favor of the common origin of all the arthropods. In proof of this, we call attention to the importance attached to the adapta- tions affecting homologous bones in fossil "horses." As it is, however, the two chelae are analogous, and not homologous, organs. Hence, technically speaking, the two chelae are utterly unrelated structures. To the eye of common sense, however, the likeness appears to be far more important than the difference, and the average person will be inclined to view the resemblance as evidence of a communuity of type. In fact, the tendency to discard superficial, and to retain only fundamental, uniformities, is dangerous to the theory of Trans- formism. When we confine our attention to what is really basic, we find that the resemblances become so generalized and widespread that specific conclusions as to descent become impossible, and we lose all sense of direction in a clueless labyrinth of innumerable, yet mutually contradictory, possi- bilities. Finally, it may be noted in passing that, though it is 62 . THE CASE AGAINST EVOLUTION customary with evolutionists to regard homologous characters as the tenaciously persistent heritage of primeval days, and to look upon adaptational characters as adventitious and ac- cessory to the aforesaid primitive heritage, the supposedly older and more fundamental characters fail to give, by the manifestation of greater fixity, any empirical evidence what- ever of their being more deeply or firmly rooted in the heredi- tary process than the presumably newer adaptational char- acters. We have, therefore, no experimental warrant for appropriating homologous, rather than adaptational, char- acters to the process of inheritance. "It is sometimes asserted," says Goodrich, "that old-established charac- ters are inherited, and that newly begotten ones are not, or are less constant, in their reappearance. This state- ment will not bear critical examination. For, on the one hand, it has been conclusively shown by experimental breeding that the newest characters may be inherited as constantly as the most ancient. . . . While, on the other hand, few charac- ters in plants can be older than the green color due to chloro- phyll, yet it is sufficient to cut off the light from a germinating seed for the greenness to fail to appear. Again, ever since Devonian times vertebrates have inherited paired eyes; yet, as Professor Stockard has shown, if a little magnesium chlo- ride is added to the sea water in which the eggs of the fish Fundulus are developing, they will give rise to embryos with one median cyclopean eye! Nor is the suggestion any hap- pier that the, so to speak, more deep-seated and fundamental characters are more constantly inherited than the trivial or superficial. A glance at the organisms around us, or the slightest experimental trial, soon convinces us that the appar- ently least important character may reappear as constantly as the most fundamental. But while an organism may live without some trivial character, it can rarely do so when a fundamental character is absent, hence such incomplete indi- viduals are seldom met in Nature." {Science, Dec. 2, 1921, p. 530.) HOMOLOGY AND ITS INTERPRETATION 63 But, whether it be upon, or beneath, the surface, similitude of any kind suffices to establish our contention that in- heritance is not the only similifying influence present in or- ganisms, and that resemblance is perfectly compatible with independence of ancestry. We have, therefore, an alternative for inheritance in the explanation of organic uniformities, and by the admission of this alternative, which, for the rest, is factually attested by the universally acknowledged phenomena of convergence, the inference of common descent from struc- tural resemblance is shorn of the last remnant of its demon- strative force, as an a posteriori argument. But a still more serious objection to the evolutionary inter- pretation of homology and preadaptation arises from its intrinsic incoherency. Evolution, as previously stated, is as- sumed to be the resultant of a twofold process, namely, in- heritance and variation. The first is a conservative and similifying process, which transmits. The second is a progres- sive and diversifying process, which diverts. To the former process are due the uniformities of homology, to the latter the deviations of adaptation. Upon the admission of evolutionists themselves, however, neither of these processes behaves in a manner consistent with its general nature, and both of them are flagrantly unfaithful to the principal roles assigned to them. Nowadays the hereditary process transmits adapta- tional, as well as homologous, characters. If, then, adapta- tional characters are more recent than homologous characters, there must have been a time when inheritance ceased to simi- lify and become a diversifying process by transmitting what it did not receive from the previous generation. There were times when, not content with simply reiterating the past, it began to divert former tendencies into novel channels. In other words, inheritance becomes dualized into a paradoxical process, which both perpetuates the old and appropriates the new. The same inconsistency is manifest in the process of variation, which capriciously produces convergent, no less than divergent, adaptations. In two fundamentally identical 64 THE CASE AGAINST EVOLUTION structures, like the wing of a bird and the foreleg of a cat, variation is said to have produced diverse adaptations. In two fundamentally diverse structures, like the head of an octopus and the head of a frog, variation is said to have produced an identical adaptation, namely, the vetebrate type of eye. It appears, therefore, that the essentially diversifying process of variation can become, on occasion, a simplifying process, which, instead of solving environmental problems in an original man- ner, prefers to employ uniform and standardized solutions, and to cling to its old stereotyped methods. Inheritance similifies and diversifies, variation converges and diverges. It is futile to attempt to reduce either of these protean processes to a con- dition that even approximates consistency. The evolutionist blows hot and cold with the same breath. Verily, his god is Proteus, or the double-headed Janus! Summa summarum: The evolutionary argument from homology is defective in three important respects: (1) in its lack of experimental confirmation; (2) in its incomplete enumeration of the disjunctive possibilities; (3) in its inability to construct a scheme of transmutation that synthesizes in- heritance and variation in a logically coherent, and factually substantiated formula. The first two defects are not neces- sarily fatal to the argument as such. Though they destroy its pretensions to conclusiveness, they do not preclude the ful- filment of the moderate claim made in its behalf by Prof. T. H. Morgan, who says: "In this sense {i.e., as previously stated) the argument from comparative anatomy, while not a demonstration, carries with it, I think, a high degree of prob- ability." ("A Critique of the Theory of Evolution," p. 14.) The third defect is more serious. The apparently irreducible antagonism which the evolutionary assumption introduces be- tween inheritance and variation has been sensed even by the adherents of transformism themselves, and they have searched in vain for a formula, which, without sacrificing the facts, would bring into concord the respective roles of these discord- ant factors. "It follows," says Osborn, "as an unprejudiced HOMOLOGY AND ITS INTERPRETATION 65 conclusion from our present evidence that upon Weismann's principle we can explain inheritance but not evolution, while with Lamarck's principle and Darwin's selection principle we can explain evolution, but not, at present, inheritance. Dis- prove Lamarck's principle and we must assume that there is some third factor in evolution of which we are ignorant." (Popular Science Monthly, Jan., 1905.) The point is well taken, and unless, as Osborn suggests, there is a tertium quid by means of which the discord can be resolved into ultimate harmony, we see no way of liberating the theory of Transmuta- tion from this embarrassing dilemma. CHAPTER III FOSSIL PEDIGREES "By dint of such great efforts we succeeded only in piecing together genial romances more or less historical." — B. Grassi, Prof, of Compara- tive Anatomy, Univ. of Rome, "La vita" (1906), p. 227. § 1. The Argument in the Abstract The palaeontological argument for evolution is based upon the observed gradual approximation in type of the earlier forms of life, as represented by the fossils still preserved in successive geological strata, to the later forms of life, as repre- sented by the contemporary species constituting our present flora and fauna. Here the observed distribution in time sup- plements and confirms the argument drawn from mere struc- tural affinity. Here we are no longer dealing with the spatial gradation of contemporary forms, arranged on a basis of greater or lesser similarity (the gradation whence the zoolo- gist derives his argument for evolution), but with a temporal gradation, which is simultaneously a morphological series and an historical record. The lower sedimentary rocks contain specimens of organic life very unlike modern species, but, the higher we ascend in the geological strata, the more closely do the fossil forms resemble our present organisms. In fact, the closeness of resemblance is directly proportional to the prox- imity in time, and this seems to create a presumption that the later forms of life are the modified descendants of the earlier forms. Considered in the abstract, at least, such an argument is obviously more formidable than the purely an- atomical argument based on the degrees of structural affinity observable in contemporary forms. It ought, therefore, to 66 FOSSIL PEDIGREES 67 be extremely persuasive, provided, of course, it proceeds in rigorous accord with indubitably established facts and rules out relentlessly the alloy of uncritical assumptions. Here, likewise, we find the theory of transformism asserting its superiority over the theory of immutability, on the ground that evolutionism can furnish a natural explanation for the gradational distribution of fossil types in the geological strata, whereas the theory of permanence resorts, it is said, to a supernaturalism of reiterated "new creations" alternating with "catastrophic exterminations." Now, if this claim is valid, and it can be shown conclusively that fixism is inevitably com- mitted to a postulate of superfluously numerous "creations," then the latter theory is shorn of all right to consideration by Occam's Razor: Entia non sunt multiplicanda sine ratione. It is rather difficult to conceive of the Creator as continually blotting out, and rewriting, the history of creation, as ruth- lessly exterminating the organisms of one age, only to repopu- late the earth subsequently with species differing but little from their extinct predecessors — ad quid perditio haecf Such procedure hardly comports with the continuity, regularity and irrevisable perfection to be expected in the works of that Divine Wisdom, which "reacheth . . . from end to end might- ily and disposeth all things sweetly" {Wisdom, viii; 1), which "ordereth all things in measure, and number and weight." (Wis. xi; 21.) Following the lead of other evolutionists, Wasmann has striven to saddle fixism with the fatuity of periodic catas- trophism and "creation on the installment plan." But even Cuvier, who is credited with having originated the theory of catastrophism, did not go to the absurd extreme of hypothe- cating reiterated creations, but sought to explain the repopu- lation of the earth after each catastrophe by means of migrations from distant regions unaffected by the catastrophe. Historically, too, fixism has had its uniformitarian, as well as its catastrophic, versions. In fact, Huxley classifies both uni- formitarianism and catastrophism as fixistic systems, when 68 THE CASE AGAINST EVOLUTION he says: "I find three more or less contradictory systems of geologic thought . . . standing side by side in Britain. I shall call one of them Catastrophism, another Uniformitarianism, the third Evolutionism." ("Lay Sermons," p. 229.) Obvi- ously, then, fixism is separable from the hypothesis of repeated catastrophes alternating with repeated "creations." Stated in proper terms, it is at one with evolutionism in re- jecting as undemonstrated and improbable the postulate of reiterated cataclysms. It freely acknowledges that, in the ab- sence of positive evidence of their occurrence, the presumption is against extraordinary events, like wholesale catastrophes. It sanctions the uniformitarian tenet that ordinary cosmic processes are to be preferred to exceptional ones as a basis of geological explanation, and it repudiates as unscientific any recourse to the unusual or the miraculous in accounting for natural phenomena. Its sole point of disagreement with evo- lutionism is its refusal to admit organic changes of specific magnitude. It does, however, admit germinal changes of varietal magnitude. It also recognizes that the external char- acters of the phenotype are the joint product of germinal fac- tors and environmental stimuli, and admits, in consequence, the possibility of purely somatic changes of considerable profun- dity being induced by widespread and persistent alterations in environmental conditions. Like Darwin, the uniformitarian fixist ascribes the origination of organic life to a single vivi- fying act on the part of the Creator, an act, however, that was formative rather than creative, because the primal forms of life, whether few or many, were all evolved through Divine influence from preexistent inorganic matter. Unlike Darwin, he ascribes the continuation of organic life to generative proc- esses that were univocal {generationes univocae) , and not gradually-equivocal {generationes paulatim aequivocae). In the next chapter, we shall see that, in attributing the initial formation of species to a Divine act, neither Darwin nor the creationists exposed themselves to the charge of explaining the "natural" by means of the "miraculous." And, as for FOSSIL PEDIGREES 69 the process by which living forms were continued upon earth, the univocal reproductive process upheld by fixism is more manifestly a natural process than the gradually-equivocal generation of variable inheritance hypothecated by the theory of transmutation. The sole matter of dispute between the two views is whether the life-cycles of organisms are circles or spirals. But all this, it will be said, is purely negative. Merely to refrain from any recourse to the extraordinary or the super- natural is by no means sufficient. ''Natural explanations" must be explanatory as well as natural. Unless there be a simplification, a reduction of plurality to unity, a resolution of many particular problems into a common general problem, we have no explanation worthy of the name. Granting, there- fore, that uniformitarian fixism does not recur to the an- omalous or the miraculous, it still lies open to the charge of failing in its function as an explanation, because it multiplies origins in both space and time. Transformism, on the contrary, is said to elucidate matters, inasmuch as it unifies origins spa- tially and temporally. That transformism successfully plausibleizes a unification of origins in space, is true only in a limited and relative sense. The most that can be said for the assumption, that resem- blances rest on the principle of common inheritance, is that it permits of a numerical reduction of origins, but this nu- merical reduction will, by an intrinsic necessity, always fall short of absolute unification. The monophyletic derivation of all organic forms from one primordial cell or protoblast is a fantastic dream, for which, from the very nature of things, natural science does not, and can not, furnish even the sem- blance of an objective basis. The ground is cut from under our feet, the moment we attempt to extend the principle of descent outside the limits of an organic phylum. The sole basis of inference is a group of uniformities, and, unless these uniformities predominate over the diversities, there can be no rational application of the principle of transformism. Hence, 70 THE CASE AGAINST EVOLUTION the hypothesis, that organisms are consanguineous notwith- standing their differences, loses all value as a solution at the point where resemblances are outweighed by diversities. The transmutation assumed to have taken place must be never so complete as to have obliterated all recognizable vestiges of the common ancestral type. "Whenever," says Driesch, "the theory that, in spite of their diversities, the organisms are related by blood, is to be really useful for explanation, it must necessarily be assumed in every case that the steps of change, which have led the specific form A to become the specific form B, have been such as only to change in part that original form A. That is to say: the similarities between A and B must never be overshadowed by their diversities." ("Science and Philosophy of the Organism," v. I, p. 254.) When, therefore, the reverse is true and diversities are preva- lent over uniformities, we are left without clue or compass in the midst of a labyrinth of innumerable possibilities. Such are the limits imposed by the very nature of the evidence itself, and the scientists, who transgress these limits, by attempting to correlate the primary phyla, are on a par with those uncon- vincible geniuses, who continually besiege the Patent Office with schemes ever new and weird for realizing the chimera of "perpetual motion." Thus scientific transformism is unable to simplify the prob- lem beyond a certain irreducible plurality of forms, lesser only in degree than the plurality postulated by fixism. This being the case, the attempts of Wasmann and Dorlodot to prune the works of Creation with Occam's Razor are not only presumptuous, but precarious as well. Qui nimis prohat, nihil probat! If it be unworthy of God to multiply organic origins in space, then monophyletic descent is the only possible alter- native, and polyphyletic transformism falls under the same condemnation as fixism. Yet the polyphyletic theory of descent is that to which both Wasmann and Dorlodot sub- scribe, as it is, likewise, the only kind of transformism which science can ever hope to plausibleize. Besides, too close a FOSSIL PEDIGREES 71 shave with Occam's Razor would eliminate creation altogether, since all theologians cheerfully admit that it was the result of a free and unnecessary act on the part of God. When we apply our rationes convenientiae to the Divine operations, we must not make the mistake of applying them to the Divine action itself instead of the created effects of that action. We may be competent to discern disorder and irregularity in finite things, but we are wholly incompetent to prescribe rules for Divine conduct. To say that God is constrained by His in- finite Wisdom to indirect, rather than direct, production, or that He must evolve a variety of forms out of living, rather than non-living, matter, is to be guilty of ridiculous anthro- pomorphism. There is no a priori reason, founded upon the Divine attributes, which restricts God's creative action to the production of this, or that, number of primordial organisms, or which obliges him to endow primitive organisms with the power of transmutation. But the fact that these rationes convenientiae fail to estab- lish the a priori necessity of a unification of organic origins in space, does not imply that they are without value in sug- gesting the unification of organic origins in time. Order and regularity are not excluded by spatial multiplicity, but they may easily be excluded by the incongruities of an irregular succession of events. Indeterminism and chance are, indeed, inseparable from the course of Nature. There is in matter an unlimited potentiality, incommensiu-ate with the limited effi- cacy of natural agencies. Hence it evades the absolute control of all finite factors and forces. But the anomalies and ir- regularities, which are contingent upon the limitation or frus- tration of second causes unable to impose an iron necessity upon evasive matter, are not referable to the First 'Cause, but rather to the finite efficacy of second causes. Such anomalies in natural processes, consequently, are not inconsistent with in- finite wisdom and power on the part of the Creator. If, on the contrary, the anomaly occurs, not in the form of an accidental frustration of a natural agency, but in the form of an intrusive 72 THE CASE AGAINST EVOLUTION "new creation," the irregularity in question would then be re- ferable to the Creator Himself, and such derogations of order are inadmissible, except as manifestations of the supernatural. In fact, the abrupt and capricious insertion of a "new crea- tion" into an order already constituted, say, for instance, the sudden introduction of Angiosperms in the Comanchian period, or of mammals in the Tertiary, would be out of harmony with both reason and revelation. Unless there is a positive reason for supposing the contrary, we must pre- sume that, subsequent to the primordial constitution of things, the Divine influence upon the world has been concurrent rather than revolutionizing. Hence a theory of origins, compatible with the simultaneous "creation" of primal organisms, is decidedly preferable to a theory, which involves successive "creations" at random. That transform- ism dispenses with the need of assuming a succession of "crea- tive" acts, is perfectly obvious, and, unless fixism can emulate its rival system in this respect, it cannot expect to receive serious attention. But once fixism assumes the simultaneousness of organic origins, it encounters, in the absence of modern organic types from ancient geological strata, a new and formidable difficulty. Cuvier's theory of numerous catastrophes followed by whole- sale migrations of the forms, which had escaped extinction, is tantamount to an appeal to the extraordinary and the im- probable for purposes of explanation, and this, as we have seen, is an expedient, which natural science is justified in refusing to sanction. Nor does the appeal to the incompleteness of the geological record offer a more satisfactory solution. It is tax enough, as we shall see, upon our credulity, when the transformist seeks to account thereby for the absence of inter- mediate types, but to account in this fashion for the absence of palaeozoic Angiosperms and mammals is asking us to be- lieve the all-but-incredible. It would not, therefore, be ad- visable for the fixist to appropriate the line of defense sug- gested for him by Bateson — "It has been asked how do you FOSSIL PEDIGREES 73 know for instance that there were no mammals in Palaeozoic times? 'May there not have been mammals somewhere on the earth though no vestige of them has come down to us? We may feel confident there were no mammals then, but are we sure? In very ancient rocks most of the great orders of animals are represented. The absence of the others might by no great stress of imagination be ascribed to accidental circumstances." But the sudden rise of the Angiosperms in the early part of the Mesozoic era is an instance of de novo origin that is not so easily explained away. Hence Bateson continues: ''Happily, however, there is one example of which we can be sure. There were no Angiosperms — that is to say 'higher plants' with protected seeds — in the carboniferous epoch. Of that age we have abundant remains of a world- wide and rich flora. The Angiosperms are cosmopolitan. By their means of dispersal they must immediately have become so. Their remains are very readily preserved. If they had been in existence on the earth in carboniferous times they must have been present with the carboniferous plants, and must have been preserved with them. Hence we may be sure that they did appear on earth since those times. We are not certain, using certain in the strict sense, that Angiosperms are the lineal descendants of the carboniferous plants, but it is much easier to believe that they are than that they are not.'' {Science, Jan. 20, 1922, p. 58.) It would thus appear, that not all the organic types of either the plant, or the animal, kingdom are of equal an- tiquity, and that the belated rise of unprecedented forms has the status of an approximate certainty, wherewith every theory of origins must inevitably reckon. How, then, is the fixist to reconcile this successive appearance of organisms with the simultaneous "creation" advocated by St. Augustine and St. Thomas of Aquin? Unless there be some other gradual process besides transmutation, to bridge the interval between the crea- tive fiat and the eventual appearance of modern types, there seems to be no escape from the dilemma. 74 THE CASE AGAINST EVOLUTION This brings us to St. Augustine's theory of the evolution of organic life from inorganic matter, which Dorlodot sophisti- cally construes as supporting the theory of descent. Accord- ing to St. Augustine, for whose view the Angelic Doctor ex- pressed a deliberate preference, the creation of the corporeal world was the result of a single creative act, having an imme- diate effect in the case of minerals, and a remote or postponed effect in the case of plants and animals (cf. *'De Genesi ad litteram," lib. V, c. 5). Living beings, therefore, were cre- ated, not in actuality, but in germ. God imparted to the ele- ments the power of producing the various plants and animals in their proper time and place. Hence living beings were cre- ated causally rather than formally, by the establishment of causal mechanisms or natural agencies especially ordained to bring about the initial formation of the ancestral forms of life. The Divine act initiating these "natural processes" {rationes seminales, rationes causales) in inorganic, and not in living, matter, was instantaneous, but the processes, which terminated in the formation of plants and animals, in their appointed time and place, were in themselves gradual and successive. Thus by an influx of Divine power the earth was made pregnant with the promise of every form of life — ^'Sicut matres gravidas sunt foetibus, sic ipse mundus est gravidus causis nascentiumJ' (Augustine, lib. Ill, ''de Trinitate," c. 9.) By reason of this doctrine, the Louvain professor claims that St. Augustine was an evolutionist, and so, indeed, he was, if by evolution is meant a gradual production of organisms from inorganic matter. But if, on the contrary, by evolution is meant a progressive differentiation and multiplication of organic species by transmutation of preexistent forms of life, or, in other words, if evolution is taken in its usual sense as synonym for transformism, then nothing could be more ab- surdly anachronistic than to ascribe the doctrine to St. Augus- tine. The subject of the gradual process postulated by the latter was, not living, but inorganic, matter, and the process was conceived as leading to the formation, and not the trans- FOSSIL PEDIGREES 76 formation, of species. The idea of variable inheritance did not occur to'St. Augustine, and he conceived organisms, once they were in existence, as being propagated exclusively by univocal reproduction {generatio univoca). It is the fixist, therefore, rather than the transformist, who is entitled to exploit the Augustinian hypothesis. In fact, it is only the vicious am- biguity and unlimited elasticity of the term evolution, which avail to extenuate the astounding confusion of ideas and total lack of historic sense, that can bracket together under a common term the ideology of Darwin and the view of St. Augustine. § 2. The Argument in the Concrete But it is our task to criticize the theory of transformism, and not to throw a life-line to fixism, by advocating gradual formation of species as the only feasible alternative to gradual transformation of species. Perhaps, this particular life-line will not be appreciated any way ; for the fixist may, not with- out reason, prefer to rest his case on the contention that the intrinsic time-value of geological formations is far too proble- matic for certain conclusions of any sort. In maintaining this position, he will have the support of some present-day geologists, and can point, as we shall see, to facts that seem to bear out his contention. In fact, the cogency of the palse- ontological argument appears to be at its maximum in the abstract, and to evaporate the moment we carry it into the concrete. The lute seems perfect, until we begin to play thereon, and then we discover certain rifts that mar the effect. It is to these rifts that our attention must now be turned. The first and most obvious flaw, in the evolutionary inter- pretation of fossil series, is the confounding of succession with filiation. Thinkers, from time immemorial, have com- mented on the deep chasm of distinction, which divides his- torical from causal sequence, and philosophers have never ceased to inveigh against the sophistical snare of: Post hoc, ergo prompter hoc. That one form of life has been subsequent 76 THE CASE AGAINST EVOLUTION in time to another form of life is, in itself, no proof of descent. "Let us suppose," says Bather, "all written records to be swept away, and an attempt made to reconstruct English history from coins. We could set out our monarchs in true order, and we might suspect that the throne was hereditary; but if on that assumption we were to make James I, the son of Elizabeth — well, but that's just what palaeontologists are constantly doing. The famous diagram of the Evolution of the Horse which Huxley used in his American lectures has had to be corrected in the light of the fuller evidence recently tabulated in a handsome volume by Prof. H. F. Osborn and his coadjutors. Palceotherium, which Huxley regarded as a direct ancestor of the horse, is now held to be only a col- lateral, as the last of the Tudors were collateral ancestors of the Stuarts. The later Ancitherium must be eliminated from the true line as a side branch — a Young Pretender. Some- times an apparent succession is due to immigration of a distant relative from some other region — 'The glorious House of Han- over and Protestant Succession.' It was, you will remember, by such migrations that Cuvier explained the renewal of life when a previous fauna had become extinct. He admitted suc- cession but not descent." {Science, Sept. 17, 1920, p. 261.) But, if succession does not imply descent, descent, at least, implies succession, and the fact that succession is the necessary corollary of descent, may be used as a corrective for the erro- neous allocations made by neontologists on the basis of purely morphological considerations. The priority of a type is the sine qua non condition of its being accepted as ancestral. It is always embarrassing when, as sometimes happens, a "de- scendant" turns out to be older than, or even coeval with, his "ancestor." If, however, the historical position of a form can be made to coincide with its anatomical pretensions to ancestry, then the inference of descent attains to a degree of logical respectability that is impossible in the case of purely zoologi- cal evidence. Recent years have witnessed a more drastic application of the historical test to morphological speculations, FOSSIL PEDIGREES 77 and the result has been a wholesale revision of former notions concerning phylogeny. ''I could easily," says Bather, "occupy the rest of this hour by discussing the profound changes wrought by this conception on our classification. It is not that orders and classes hitherto unknown have been discov- ered, not that some erroneous allocations have been corrected, but the whole basis of our system is being shifted. So long as we were dealing with a horizontal section across the tree of life — that is to say, with an assemblage of approximately contemporaneous forms — or even with a number of such hori- zontal sections, so long were we confined to simple description. Any attempt to frame a causal connection was bound to be speculative." {Ibidem, p. 258.) Whether zoologists will take kindly to this ''shifting of the whole basis" of classification, remains to be seen. Personally, we think they would be very ill-advised to exchange the solid observational basis of homol- ogy for the scanty facts and fanciful interpretations of palaeontologists. The second stumblingblock in the path of Transformism is the occurrence of convergence. We have seen that, in the palseontological argument, descent is inferred conjointly from similarity and succession, and that, in the abstract, this argu- ment is very persuasive. One of the concrete phenomena, however, that tend to make it inconsequential, is the undoubted occurrence of convergence. Prof. H. Woods of Cambridge, in the Introduction to the 5th edition of his "Palaeontology" (1919), speaks of three kinds of convergence (cf., pp. 14, 15, 16), which, as a matter of convenience, we may term the parallelistic, the radical, and the adaptational, types of con- vergence. A brief description of each type will serve to elu- cidate its nature and its significance : (1) Parallelistic convergence implies the appearance of parallel modifications in the homologous parts of organisms regarded as diverging from common stock in two distinct col- lateral lines, that were independent at the time of the ap- pearance in both of the said parallel modifications. Speaking 78 THE CASE AGAINST EVOLUTION of the fossil ccelenterates known as Graptolites, Professor Woods says: "In some genera the hydrothecae of dif- ferent species show great variety of form, those of one species being often much more like those of a species belonging to another genus than to other species of the same genus." ("Palaeontology," 5th ed., 1919, p. 69.) As another instance of this phenomenon, the case of the fossil ungulates of South America, spoken of as Litoptema, may be cited, and the case is peculiarly interesting because of its bearing on that piece de resistance of palaeontological evidence, the Pedigree of the Horse. "The second family of Litoptema," says Wm. B. Scott, "the Proterotheriidae, were remarkable for their many decep- tive resemblances to horses. Even though those who contend that the Litoptema should be included in the Perissodactyla should prove to be in the right, there can be no doubt that the proterotheres were not closely related to the horses, but formed a most striking illustration of the independent acqui- sition of similar characters through parallel or convergent development. The family was not represented in the Pleisto- cene, having died out before that epoch, and the latest known members of it lived in the upper Pliocene. . . . Not that this remarkable character was due to grotesque proportions; on the contrary, they looked far more like the ordinary ungulates of the northern hemisphere than did any of their South Ameri- can contemporaries; it is precisely this resemblance that is so notable. . . . The feet were three-toed, except in one genus (Thoatherium) in which they were single-toed, and nearly or quite the whole weight was carried upon the median digit, the laterals being mere dew-claws. The shape of the hoofs and the whole appearance of the foot was surprisingly like those of the three-toed horses, but there were certain structural dif- ferences of such great importance, in my judgment, as to forbid the reference of these animals, not merely to the horses, but even to the perissodactyls." ("A History of Land Mammals in the Western Hemisphere," p. 499.) For this sort of parallelism, the Lamarckian and Darwinian FOSSIL PEDIGREES 79 types of evolution by addition can offer no rational explana- tion. It 'could, perhaps, be accounted for upon the Bateso- nian hypothesis of evolution by loss of inhibition, that is to say, the coincident appearance of convergent characters in collateral lines might be interpreted as being due to a parallel loss in both lines of the inhibitive genes, which had sup- pressed the convergent feature in the primitive or common stock. We say that the convergence might be so interpreted, because the interpretation in question would, at best, be merely optional and not at all necessary; for in the third, or adapta- tional, type of convergence, we shall see instances of parallel modifications occurring in completely independent races, whose morphology and history alike exclude all possibility of heredi- tary connection between them. Hence, even in the present case, nothing constrains us to accept the genetic interpretation. (2) Radical convergence, which Woods styles heterogenetic homoeomorphy, is described by him as follows: "Sometimes two groups of individuals resemble each other so closely that they might be regarded as belonging to the same genus or even to the same species (italics mine), but they have de- scended from different ancestors since they are found to differ in development (ontogeny) or in their palaeontological history; this phenomenon, of forms belonging to different stocks ap- proaching one another in character, is known as convergence or heterogenetic homoeomorphy, and may occur at the same geo- logical period or at widely separated intervals. Thus the form of oyster known as Gryphaea has originated independently from oysters of the ordinary type in the Lias, in the Oolites, and again in the Chalk; these forms found at different horizons closely resemble one another and have usually been regarded as belonging to one genus (Gryphaea) , but they have no direct genetic connection with one another." ("Palaeontology," 5th ed., 1919, p. 15.) Comment is almost superfluous. If even specific resemblance is no proof of common origin, then what right have we to interpret any resemblance whatever in this sense? With such an admission, the whole bottom drops out 80 THE CASE AGAINST EVOLUTION of the evolutionary argument. When the theory of descent is forced to account for heterogenetic resemblance at expense of all likelihood and consistency, when it cannot save itself except by blowing hot and cold with one breath, one is tempted to exclaim: "Oh, why bother with it!" (3) Adaptational convergence is the occurrence of parallel modifications due to analogous specialization in unrelated forms, whose phylogeny has been obviously diverse. ''Also, animals belonging to quite distinct groups," says Woods, "may, when living under similar conditions, come to resemble one another owing to the development of adaptive modifications, though they do not really approach one another in essential characters ; thus analogous or parallel modifications may occur in independent groups — such are the resemblances between flying reptiles {Ornithosaurs) and birds, and between sharks, icthyosaurs and dolphins." (Op. cit., p. 16.) As this type of convergence has been discussed in a previous article, with reference to the mole and mole-cricket, it need not detain us further. All these types of convergence, but especially the second type, are factual evidence of the compatibility of resemblance with independent origin, and the fact of their occurrence tends to undermine the certainty of the phylogenetic inferences based on fossil evidence ; all the more so, that, thanks to its bad state of preservation, and the impossibility of dissection, even super- ficial resemblances may give rise to false interpretations. And, as for the cases of radical convergence, there is no denying that they strike at the very heart of the theory of descent. The third difiiculty for Transformism arises from the dis- continuity of the geological record. It was one of the very first discrepancies to be discovered between evolutionary ex- pectation and the actual results of research. The earliest ex- plorations revealed a state of affairs, that subsequent investi- gations have failed to remedy: on the one hand, namely, a notable absence of intermediate species to bridge the gaps between the fossil genera, and on the other hand, the sudden FOSSIL PEDIGREES 81 and simultaneous appearance of numerous new and allied types unheralded by transitional forms. Since Darwin had stressed the gradualness of transmutation, the investigators expected to find the transitional means more numerous than the terminal extremes, and were surprised to find, in the real record of the past, the exact reverse of their anticipation. They found that the classes and families of animals and plants had always been as widely separated and as sharply differentiated as they are to-day, and that they had always formed distinct systems, un- connected by transitional links. The hypothetical "generalized types," supposed to combine the features of two or three fam- ilies, have never been found, and most probably never will be; for it is all but certain that they never existed. Occasionally, it is true, palaeontologists have discovered isolated types, which they interpreted as annectant forms, but a single pier does not make a bridge, and only too often it chanced that the so-called annectant type, though satisfactory from the mor- phological standpoint, was more recent than the two groups, to which it was supposed to be ancestral. But it will make matters plainer, if we illustrate what is meant by the discon- tinuity or incompleteness of the fossil record, by reference to some concrete series, such as the so-called Pedigree of the Horse. Whenever a series of fossils, arranged in the order of their historical sequence, exhibits a gradation of increasing resem- blance to the latest form, with which the series terminates, such a series is called a palaeontological pedigree, and is said to represent so many stages in the racial development or phylogeny of the respective mx)dern type. The classical example of this sort of "pedigree" is that of the Horse. It is, perhaps, one of the most complete among fossil "genealogies," and yet, as has been frequently pointed out, it is, as it stands, extremely incomplete. Modern representatives of the Equidaey namely, the horse, the ass and the zebra, belong to a common genus, and are separated from one another by differences which are merely specific, but the differences which separate 82 THE CASE AGAINST EVOLUTION the various forms, that compose the "pedigree of the Horse," are generic. We have, to borrow Gerard's simile, nothing more than the piers of the evolutionary bridge, without the arches, and we do not know whether there ever were any arches. There is, indeed, a sort of progression, e.g., from the four- toed to a one-toed type, so that the morphological gradation does, in some degree, coincide with temporal succession. But, on the other hand, the fossil forms, interpreted as stages in the phylogeny of the Horse, are separated from one another by gaps so enormous, that, in the absence of intermediate spe- cies to bridge the intervals, it is practically impossible, par- ticularly in the light of our experimental knowledge of Gen- etics, to conceive of any transition between them. Nor is this all. The difficulty is increased tenfold, when we attempt to relate the Equidae to other mammalian groups. Fossil un- gulates appear suddenly and contemporaneously in the Ter- tiary of North America, South America and Europe, without any transitional precursors, to connect them with the hypo- thetical proto-mammalian stock, and to substantiate their collaterality with other mammalian stocks. To all such difficulties the evolutionist replies by alleging the incompleteness of the geological record, and modern hand- books on palaeontology devote many pages to the task of explaining why incompleteness of the fossil record is just what we should expect, especially in the case of terrestrial animals. The reasons which they assign are convincing, but this particular mode of solving the difficulty is a rather pre- carious one. Evolutionists should not forget that, in sacri- ficing the substantial completeness of the record to account for the absence of intermediate species, they are simultaneously destroying its value as a proof of the relative position of organic types in time. Yet this, as we have seen, is precisely the feature of greatest strategic value in the palaeontological "evidence" for evolution. We must have absolute certainty that the reputed "ancestor" was in existence prior to the ap- pearance of the alleged "descendant," or the peculiar force of FOSSIL PEDIGREES 83 the palseontological argument is lost. It would be prepos- terous for the progeny to be prior to, or even coeval with, the progenitor, and so we must be quite sure that what we call "posterity" is really posterior in time. Now the sole argu- ment that palaeontology can adduce for the posteriority of one organic type as compared with another is the negative evidence of its non-occurrence, or rather of its non-discovery, in an earlier geological formation. The lower strata do not, so far as is known, contain the type in question, and so it is con- cluded that this particular form had no earlier history. Such an inference, as is clear, is not only liable to be upset by later discoveries, but has the additional disadvantage of implicitly assuming the substantial completeness of the fossil record, whereas the absence of intermediate species is only explicable by means of the assumed incompleteness of the selfsame record. The evolutionist is thus placed in the dilenm:ia of choosing between a substantially complete, and a substantially incom- plete, record. Which of the alternatives, he elects, matters very little; but he must abide by the consequences of his de- cision, he cannot eat his cake and have it. When the evolutionist appeals to the facts of palaeontology, it goes without saying that he does so in the hope of showing that the differences, which divide modern species of plants and animals, diminish as we go backward in time, until the stage of identity is reached in the unity of a common ancestral type. Hence from the very nature of the argument, which he is engaged in constructing, he is compelled to resort to intermediate types as evidence of ^the continuity of allied spe- cies with the hypothetical ancestor, or common type, whence they are said to have diverged. Now, even supposing that his efforts in this direction were attended with a complete measure of success, evidence of this kind would not of itself, as we shall see, suffice to demonstrate the common origin of the extremes, between which a perfect series of intergradent types can be shown to mediate. Unquestionably, however, unless such a series of intergradent fossil species can be adduced as 84 THE CASE AGAINST EVOLUTION evidence of the assumed transition, the presumption is totally against the hypothesis of transformism. Now, as a matter of fact, the geological record rarely offers any evidence of the existence in the past of intermediate species. For those, who have implicit confidence in the time- value of geological "formations," there are indications of a general advance from lower to higher forms, but, even so, there is little to show that this seeming progress is to be interpreted as an increasing divergence from common ancestral types. With but few exceptions, the fossil record fails to show any trace of transitional links. Yet pedigrees made up of diverse genera are poor evidence for filiation or genetic con- tinuity, so long as no intermediate species can be found to bridge the chasm of generic difference. By intermediate spe- cies, we do not mean the fabulous "generalized type." An- nectants of this kind are mere abstractions, which have never existed, and never could have existed. We refer rather to actual fossil types separated from one another by differences not greater than specific ; for "not until we have linked species into lineages," can fossil pedigrees lay claim to serious attention. But let us suppose the case for evolution to be ideally favor- able, and assume that in every instance we possessed a perfect gradation of forms between two extremes, such, for example, as occurs in the Ammonite series, even then we would be far from having a true demonstration of the point at issue. Bate- son has called our attention to the danger of confounding sterile and instable hybrids with intergradent species. "Ex- amine," he says, "any two thoroughly distinct species which meet each other in their distribution, as for instance. Lychnis diurna and vespertina do. In areas of overlap are many inter- mediate forms. These used to be taken to be transitional steps, and the specific distinctness of vespertina and diurna was on that account questioned. Once it is known that these supposed intergrades are merely mongrels between the two species the transition from one to the other is practically be- FOSSIL PEDIGREES 85 yond our powers of imagination to conceive. If both these can survive,- why has their common parent perished? Why, when they cross, do they not reconstruct it instead of producing partially sterile hybrids? I take this example to show how entirely the facts were formerly misrepresented." {Heredity, Smithson. Inst. Rpt. for 1915, p. 369.) Similarly, T. H. Morgan has shown, with reference to mutants, the fallacy of inferring common descent from the phenomenon of intergradence, and what holds true for a series of intergradent mutants would presumably also hold true of a series of intergradent species, could such a series be found and critically distinguished from hybrid and mutational inter- mediates. In short, the Darwinian deduction of common ori- gin from the existence of intergradence must now be regarded as a thoroughly discredited argument. "Because we can often arrange the series of structures in a line extending from the very simple to the more complex, we are apt to become unduly impressed by this fact and conclude that if we found the complete series we should find all the intermediate steps and that they have arisen in the order of their complexity. This conclusion is not necessarily correct." (''A Critique of the Theory of Evolution," p. 9.) Having cited such a series of gradational mutations ranging between the long-winged, and completely wingless condition, in the case of the Vinegar Fly {Drosophila melanog aster) , as well as two similar graded series based on pigmentation and eye color, he concludes: '^These types, with the fluctuations that occur within each type, furnish a complete series of gradations; yet historically they have arisen independently of each other. Many changes in eye color have appeared. As many as thirty or more races differing in eye color are now maintained in our cultures. Some of them are so similar that they can scarcely be sepa- rated from each other. It is easily possible beginning with the darkest eye color, sepia, which is a deep brown, to pick out a perfectly graded series ending with pure white eyes. But such a serial arrangement would give a totally false idea 86 THE CASE AGAINST EVOLUTION of the way the different types have arisen; and any conclu- sion based on the existence of such a series might very well be entirely erroneous, for the fact that such a series exists bears no relation to the order in which its members have ap- peared." {Op. cit., pp. 12, 13.) Such facts must give us pause in attaching undue importance to phenomena like the occurrence of a gradual complication of sutures in the Chalk Ammonites, particularly as parallel series of perfectly similar sutures occurs ''by convergence" in the fossil Ceratites, which have no genetic connection with the Ammonites. (Cf. Woods^ 'Talseontology," 5th ed., p. 16.) But, if even mutational and specific intergradents are not sufiicient evidence of common ancestry, what shall we say of a discontinuous series, whose links are separate genera, orders, or even classes, instead of species. Even the most enthusi- astic transformist is forced to admit the justice of our insistence that the gaps which separate the members of a series must be reduced from differences of the generic, to differences of the specific, order, before that series can command any respect as hypothetical "genealogy." "You will have observed," says F. A. Bather, "that the precise methods of the modern palaeontol- ogist, on which this proof is based, are very different from the slap-dash conclusions of forty years ago. The discovery of Ar- chceopteryx, for instance, was thought to prove the evolution of birds from reptiles. No doubt it rendered that conclusion extremely probable, especially if the major promise — that evo- lution was the method — were assumed. But the fact of evolu- tion is precisely what men were then trying to prove. These jumpings from class to class or from era to era, by aid of a few isolated stepping-stones, were what Bacon calls anticipa- tions "hasty and premature but very effective, because as they are collected from a few instances, and mostly from those which are of familiar occurrence, they immediately dazzle the intellect and fill the imagination." {Nov. Org., I, 28.) No secure step was taken until the modem palaeontologist began to affiliate mutation with mutation and species with FOSSIL PEDIGREES 87 species, working his way back, literally inch by inch, through a single small group of strata. Only thus could he base on the kboriously collected facts a single true interpretation; and to those who preferred the broad path of generality his interpretations seemed, as Bacon says they always "must seem, harsh and discordant — almost like mysteries of faith." . . . Thus by degrees we reject the old slippery stepping-stones that so often toppled us into the stream, and, foot by foot, we build a secure bridge over the waters of ignorance." {Science, Sept. 17, 1920, pp. 263, 264.) We cannot share Bather's confidence in the security of a bridge composed of even linked species. Let such a series be never so perfect, let the gradation be never so minute, as it might conceivably be made, when not merely distinct species, but also hybrids, mutants and fluctuants are available as stop- gaps, the bare fact of such intergradation tells nothing what- ever concerning the problem of genetical origin and specific relationship. The species-by-species method does, however, represent the very minimum of requirement imposed upon the palaeontologist, who professes to construct a fossil pedigree. But, when all is said and done, such a method, even at its best, falls considerably short of the mark. However perfectly intergradent a series of fossils may be, the fact remains that these petrified remnants of former life cannot be subjected to breeding tests, and that, in the consequent absence of geneti- cal experimentation, we have no means of determining the real bearing of these facts upon the problem of interspecific re- lationship. Only the somatic characters of extinct floras and faunas have been conserved in the rock record of the past, and even these are often rendered dubious, as we shall see pres- ently, by their imperfect state of preservation. Now, it is solely in conjunction with breeding experiments, that somatic char- acters can give us any insight into the nature of the germinal constitution of an organism, which, after all, is the cardinal consideration upon which the whole question of interspecific re- lationship hinges. All inferences, therefore, regarding the de- 88 THE CASE AGAINST EVOLUTION scent of fossil forms are irremediably speculative and conjec- tural. When we are dealing with living forms, we can always check up the inferences based on somatic characteristics by means of genetical experiments, and in so doing we have found that it is as unsafe to judge of an organism from the exclusive standpoint of its external characters as it is to judge of a book by the cover; for, apart from the check of breeding tests, it is impossible to say just which somatic characters are geneti- cally significant, and which are not. Forms externally alike may be so unlike in germinal constitution as to be sexually incompatible; forms externally unlike may be readily crossed without any discernible diminution of fertility. ''Who could have foreseen," exclaims Bateson, ''that the apple and the pear — so like each other that their botanical differences are eva- sive — could not be crossed together, though species of Antir- rhinum (Snapdragon) so totally unlike each other as ma jus and moUe can be hybridized, as Baur has shown, without a sign of impaired fertility?" {Heredity, Smithson. Inst. Rpt. for 1915, p. 370.) We cannot distinguish between alleged spe- cific, and merely mutational (varietal), change, nor between hybridizations and factorial, chromosomal, or pseudo-, muta- tions, solely on the basis of such external characters as are preserved for us in fossils. It is impossible, therefore, to demonstrate trans-specific variation by any evidence that Palaeontology can supply. The palaeontologist {pace Os- born) is utterly incompetent to pass judgment on the problem of interspecific relationship. As Bateson remarks: "In dis- cussing the physiological problem of interspecific relationship evidence of a more stringent character is now required; and a naturalist acquainted with genetical discoveries would be as reluctant to draw conclusions as to the specific relationship of a series of fossils as a chemist would be to pronounce on the nature of a series of unknown compounds from an inspection of them in a row of bottles." {Science, April 17, 1922, p. 373.) "When t"he modern student of variation and heredity," says T. H. Morgan, "looks over the different 'continuous' FOSSIL PEDIGREES 89 series, from which certain 'laws' and 'principles' have been deduced, he is struck by two facts: that the gaps, in some cases, are enormous as compared with the single changes with which he is familiar, and (what is more important) that they involve numerous parts in many ways. The geneticist says to the palaeontologist, since you do not know, and from the nature of your case can never know, whether your dif- ferences are due to one change or to a thousand, you cannot with certainty tell us anything about the hereditary units which have made the process of evolution possible." {Op. cit, pp. 26, 27.) And without accurate knowledge on this subject, we may add, there is no possibility of demonstrating specific change or genetic relationship in the case of any given fossil. In our discussion of the third defect in the fossil "evidence," allusion was made to a fourth, namely, its imperfect state of preservation. The stone record of bygone days has been so defaced by the metamorphism of rocks, by the solvent action of percolating waters, by erosion, weathering and other factors of destruction, that, like a faded manuscript, it becomes, even apart from its actual lacunae, exceedingly difficult to decipher. So unsatisfactory, indeed, is the condition of the partially ob- literated facts that human curiosity, piqued at their baffling ambiguity, calls upon human imagination to supply what ob- servation itself fails to reveal. Nor does the invitation remain unheeded. Romance hastens to the rescue of uncertain Sci- ence, with an impressive display of "reconstructed fossils," and the hesitation of critical caution is superseded by the dogmatism of arbitrary assumption. Scattered fragments of fossilized bones are integrated into skeletons and clothed by the magic of creative fancy with an appropriate musculature and flesh, reenacting for us the marvelous vision of Ezekiel: "And the bones came together, each one to its joint. And I beheld and, lo, there were sinews upon them, and the flesh came upon them: and the skin was stretched over them." (Chap. XXXVII, 7, 8.) "It is also true," says Osborn (who, like Haeckel, evinces a veritable mania for "retouching" in- 90 THE CASE AGAINST EVOLUTION complete facts) , ''that we know the mode of origin of the hu- man species; our knowledge of human evolution has reached a point not only where a number of links are thoroughly- known but the characters of the missing links can be very clearly predicated." {Science, Feb. 24, 1922.) We will not dispute his contention; for it is perfectly true, that, in each and every case, all the missing details can be so exactly predi- cated that the resulting description might well put to shame the account of a contemporary eyewitness. The only diffi- culty is that such predication is the fruit of pure imagination. Scientific reconstructions, whether in the literary, plastic, or pictorial, form, are no more scientific than historical novels are historical. Both are the outcome of a psychological weakness in the human makeup, namely, its craving for a ''finished picture" — a craving, however, that is never gratified save at the expense of the fragmentary basis of objective fact.* In calling into question, however, the scientific value of the so-called "scientific reconstruction," so far as its pretensions to precision and finality are concerned, it is not our intention to discredit those tentative restorations based upon Cuvier's Law of Correlation, provided they profess to be no more than provisional approximations. Many of the structural features of organisms are physiologically interdependent, and there is frequently a close correlation among organs and organ-sys- tems, between which no causal connection or direct physiologi- cal dependence is demonstrable. In virtue of this principle, one structural feature may connote another, in which case it would be legitimate to supply by inference any missing struc- ture implied in the actual existence of its respective correlative. But if any one imagines that the law of correlation enables a scientist to restore the lost integrity of fossil types with any considerable degree of accuracy and finality, he greatly over- estimates the scope of the principle in question. At best it is nothing more than an empirical generalization, which must not be pressed to an extent unwarranted by the inductive process, that first established it. "Certain relations of struc- '•'- See Addenda. FOSSIL PEDIGREES 91 ture," says Bather, "as of cloven hoofs and horns with a rumi- nant stomach, were observed, but as Cuvier himself insisted, the laws based on such facts were purely empirical." (*Sa- ence, Sept. 17, 1920, p. 258.) The palaeontologist, then, is justified in making use of correlation for the purpose of re- constructing a whole animal out of a few fragmentary remains, but to look for anything like photographic precision in such ''restorations" of extinct forms is to manifest a more or less complete ignorance of the nature and scope of the empirical laws, upon which they are based. The imprudence of taking these "reconstructions" of extinct forms too seriously, however, is inculcated not merely by theo- retical considerations, but by experience as well. Even in the case of the mammoth, a comparatively recent form, whose skeletal remains had been preserved more completely and per- fectly than those of other fossil types, the discovery of a com- plete carcass buried in the ice of the Siberian "taiga" on the Beresovka river showed the existing restorations to be false in important respects. All, without exception, stood in need of revision, proving, once and for all, the inadequacy of fossil remains as a basis for exact reconstruction. E. Pfizenmayer, a member of the investigating expedition, comments on the fact as follows: "In the light of our present knowledge of the mam- moth, and especially of its exterior, the various existing at- tempts at a restoration need important corrections. Apart from the many fanciful sketches intended to portray the exterior of the animal, all the more carefully made restorations show the faults of the skeleton, hitherto regarded as typical, on which they are based, especially the powerful semicircular and up- ward-curved tusks, the long tail, etc. "As these false conceptions of the exterior of the mammoth, both written and in the form of pictures, are contained in all zoological and palseontological textbooks, and even in scien- tific monographs, it seems necessary to construct a more nearly correct picture, based on our present knowledge. I have ven- tured on this task, because as a member of the latest expe- 92 THE CASE AGAINST EVOLUTION dition for mammoth remains, I was permitted not only to become acquainted with this newest find while still in its place of deposit and to take part in exhuming it, but also to visit the zoological museum of St. Petersburg, which is so rich in mammoth remains, for the purpose of studying the ani- mal more in detail." (Smithson. Inst. Rpt. for 1906, pp. 321, 322.) The example is but one of many, which serve to empha- size not merely the inadequacy of the generality of palseonto- logical restorations, but also the extreme diflficulty which the palaeontologist experiences in interpreting aright the par- tially effaced record of a vanished past. The fifth and most critical flaw in the fossil "evidence" for evolution is to be found in the anomalies of the actual dis- tribution of fossils in time. It is the boast of evolutionary Palaeontology that it is able to enhance the cogency of the argument from mere structural resemblance by showing, that, of two structurally allied forms, one is more ancient than the other, and may, therefore, be presumed to be ancestral to the later form. Antecedence in time is the sine qua non qualifica- tion of a credible ancestor, and, unless the relative priority of certain organic types, as compared with others, can be estab- lished with absolute certainty, the whole palaeontological ar- gument collapses, and the boast of evolutionary geology be- comes an empty vaunt. Whenever the appearance of a so-called annectant type is antedated by that of the two forms, which it is supposed to connect, this fact is, naturally, a deathblow to its claim of being the "common ancestor," even though, from a purely mor- phological standpoint, it should possess all the requisites of an ancestral type. Commenting upon the statement that a certain genus "is a truly annectant form uniting the Melo- crinidae and the Platycrinidae," Bather takes exception as follows: "The genus in question appeared, so far as we know, rather late in the Lower Carboniferous, whereas both Platy- crinidae and Melocrinidae were already established in Middle Silurian time. How is it possible that the far later form FOSSIL PEDIGREES 93 should unite these two ancient families? Even a mesalliance is inconceivable." {Science, Sept. 17, 1920, p. 260.) Certainty, therefore, with respect to the comparative an- tiquity of the fossiliferous strata is the indispensable presup- position of any palaeontological argument attempting to show that there is a gradual approximation of ancient, to modern, types. Yet, of all scientific methods of reckoning, none is less calculated to inspire confidence, none less safeguarded from the abuses of subjectivism and arbitrary interpretation, than that by which the relative age of the sedimentary rocks is determined! In order to date the strata of any given series with reference to one another, the palaeontologist starts with the principle that, in an undisturbed area, the deeper sediments have been deposited at an earlier period than the overlying strata. Such a criterion, however, is obviously restricted in its application to local areas, and is available only at regions of outcrop, where a vertical section of the strata is visibly ex- posed. To trace the physical continuity, however, of the strata (if such continuity there be) from one continent to another, or even across a single continent, is evidently out of the question. Hence, to correlate the sedimentary rocks of a given region with those of another region far distant from the for- mer, some criterion other than stratigraphy is required. To supply this want, recourse has been had to index fossils, which have now come into general use as age-markers and means of stratigraphical correlation, where the criterion of super- position is either absent or inapplicable. Certain fossil types are assumed to be infallibly indicative of certain stratigraphi- cal horizons. In fact, when it comes to a decision as to the priority or posteriority of a given geological formation, index fossils constitute the court of last appeal, and even the evi- dences of actual stratigraphical sequence and of physical tex- ture itself are always discounted and explained away, whenever they chance to conflict with the presumption that certain fossil forms are typical of certain geological periods. If, for ex- 94 THE CASE AGAINST EVOLUTION ample, the superposed rock contains fossils alleged to be typi- cal of an "earlier" stratigraphic horizon than that to which the fossils of the subjacent rock belong, the former is pro- nounced to be "older," despite the fact that the actual strati- graphic order conveys the opposite impression. "We still regard fossils," says J. W. Judd, "as the 'medals of creation,' and certain types of life we take to be as truly characteristic of definite periods as the coins which bear the image and superscription of a Roman emperor or of a Saxon king." (Cf. Smithson. Inst. Rpt. for 1912, p. 356.) Thus it comes to pass, in the last analysis, that fossils, on the one hand, are dated according to the consecutive strata, in which they occur, and strata, on the other hand, are dated according to the fossils which they contain. Such procedure, if not actually tantamount to a vicious circle, is, to say the least, in imminent danger of becoming so. For, even assuming the so-called empirical generalization, that makes certain fossils typical of certain definitely-aged geolog- ical "formations," to be based upon induction sufficiently com- plete and analytic to insure certainty, at least, in the majority of instances, and taking it for granted that we are dealing with a case, where the actual evidence of stratigraphy is not in open conflict with that of the index fossils, who does not see that such a system of chronology lends itself only too readily to manipulation of the most arbitrary kind, whenever the pet preconceptions of the evolutionary chronologist are at stake? How, then, can we be sure, in a given case, that a verdict based exclusively on the "evidence" of index fossils will be reliably objective? It is to be expected that the evolutionist will refrain from the temptation to give himself the benefit of every doubt? Will there not be an almost irresistible ten- dency on the part of the convinced transformist to revise the age of any deposit, which happens to contain fossils that, ac- cording to his theory, ought not to occur at the time hitherto assigned? The citation of a concrete example will serve to make our FOSSIL PEDIGREES 95 meaning clear. A series of fresh-water strata occur in India known as the Siwahk beds. The formation in question was originally classed as Miocene. Later on, however, as a result, presumably, of the embarrassing discovery of the genus Equus among the fossils of the Upper Siwalik beds, Wm. Blanford saw fit to mend matters by distinguishing the Upper, from the Lower, beds and assigning the former (which contain fos- sil horses) to the Pliocene period. The title Miocene being restricted by this ingenious step to beds destitute of equine remains, namely the Nahun, or Lower Siwalik, deposits, all danger of the horse proving to be older than his ancestors was happily averted. A mere shifting of the conventional labels, apparently, was amply sufficient to render groundless the fear, to which Professor A. Sedgwick had given expression in the following terms: "The genus Equus appears in the upper Siwalik beds, which have been ascribed to the Miocene age. ... If Equus really existed in the Upper Miocene, it was antecedent to some of its supposed ancestors." ("Stu- dents' Textbook of Zoology," p. 599.) Evidently, the Horse must reconcile himself perforce to the pedi^ee assigned to him by the American Museum of Natural History; for he is to be given but scant opportunity of escaping it. This classic genealogy has already entailed far too great an expenditure of time, money and erudition to permit of any reconsidera- tion; and should it chance, in the ironic perversity of things, that the Horse has been so inconsiderate as to leave indubi- table traces of himself in any formation earlier than the Pliocene, it goes without saying that the formation in question will at once be dated ahead, in order to secure for the "an- cestors" that priority which is their due. An elastic criterion like the index fossil is admirably adapted for readjustments of this sort, and the evolutionist who uses it need never fear defeat. The game he plays can never be a losing one, because he gives no other terms than: Heads I win, tails you lose. In setting forth the foregoing difficulties, we have purposely refrained from challenging the cardinal dogma of orthodox 96 THE CASE AGAINST EVOLUTION palaeontology concerning the unimpeachable time-value of in- dex fossils as age-markers. The force of these considerations, therefore, must be acknowledged even by the most fanatical adherents of the aforesaid dogma. Our forbearance in this instance, however, must not be construed as a confession that the dogma in question is really unassailable. On the contrary, not only is it not invulnerable, but there are many and weighty reasons for rejecting it lock, stock, and barrel. The palseontological dogma, to which we refer, is reducible to the following tenets: (1) The earth is swathed with fossil- iferous strata, in much the same fashion that an onion is cov- ered with a succession of coats, and these strata are universal over the whole globe, occurring always in the same invariable order and characterized not by any peculiar uniformity of external appearance, physical texture, or mineral composition, but solely by peculiar groups of fossil types, which enable us to distinguish between strata of different ages and to cor- relate the strata of one continent with their counterparts in another continent — "Even the minuter divisions," says Scott, ''the substages and zones of the European Jura, are applicable to the classification of the South American beds." ("Intro- duction to Geology," p. 681.) (2) In determining the relative age of a given geological formation, its characteristic fossils form the exclusive basis of decision, and all other considera- tions, whether lithological or stratigraphic, are subordinated to this — "The character of the rocks," says H. S. Williams, "their composition or their mineral contents have nothing to do with settling the question as to the particular system to which the new rocks belong. The fossils alone are the means of correlation." ("Geological Biology," pp. 37, 38.) To those habituated to the common notion that stratigraph- ical sequence is the foremost consideration in deciding the comparative age of rocks, the following statement of Sir Archi- bald Geikie will come as a distinct shock: "We may even demonstrate," he avers, "that in some mountainous ground the strata have been turned completely upside down, if we can FOSSIL PEDIGREES 97 show that the fossils in what are now the uppermost layers ought properly to lie underneath those in the beds below them." ("Textbook," ed. of 1903, p. 837.) In fact, the palaeontologist, H. A. Nicholson, lays it down as a general principle that, wher- ever the physical evidence (founded on stratigraphy and lithology) is at variance with the biological evidence (founded on the presence of typical fossil organisms), the latter must prevail and the former must be ignored: "It may even be said," he tells us, "that in any case where there should ap- pear to be a clear and decisive discordance between the physical and the palaeontological evidence as to the age of a given series of beds, it is the former that is to be distrusted rather than the latter." ("Ancient Life History of the Earth," p. 40.) George McCready Price, Professor of Geology at a denomi- national college in Kansas, devotes more than fifty pages of his recent work, "The New Geology" (1923), to an intensely destructive criticism of this dogma of the supremacy of fossil evidence as a means of determining the relative age of strata. To cite Price as an "authority" would, of course, be futile. All orthodox geologists have long since anathematized him, and outlawed him from respectable geological society. Charles Schuchert of Yale refers to him as "a fundamentalist har- boring a geological nightmare." {Science, May 30, 1924, p. 487.) Arthur M. Miller of Kentucky University speaks of him as "the man who, while a member of no scientific body and absolutely unknown in scientific circles, has . . . had the effrontery to style himself a 'geologist.' " {Science, June 30, 1922, pp. 702, 703.) Miller, however, is just enough to admit that he is well-informed on his subject, and that he possesses the gift of persuasive presentation. "He shows," says Miller, "a wide familiarity with geological literature, quoting largely from the most eminent authorities in this country and in Europe. Any one reading these writings of Price, which pos- sess a certain charm of literary style, and indicate on the part of the author a gift of popular presentation which makes 98 THE CASE AGAINST EVOLUTION one regret that it had not been devoted to a more laudable purpose, must constantly marvel at the character of mind of the man who can so go into the literature of the subject and still continue to hold such preposterous opinions." {Loc. cit., p. 702.) In the present instance, however, our interest centers, not on the unimportant question of his official status in geological circles, but exclusively on the objective validity of his argu- ment against the chronometric value of the index fossil. All citations, therefore, from his work will be supported, in the sequel, by collateral testimony from other authors of recog- nized standing. It is possible, of course, to inject irrelevant issues. Price, for example, follows Sir Henry Howorth in his endeavor to substitute an aqueous catastrophe for the glacia- tion of the Quaternary Ice Age, and he adduces many in- teresting facts to justify his preference for a deluge. But this is neither here nor there; for we are not concerned with the merits of his "new catastrophism." It is his opportune revival in modern form of the forgotten, but extremely effective, objection raised by Huxley and Spencer against the alleged universality of synchronously deposited fossiliferous sediments, that constitutes our sole preoccupation here. It is Price's merit to have shown that, in the light of recently discovered facts, such as "deceptive conformities" and "overthrusts," this objection is far graver than it was when first formulated by the authors in question. Mere snobbery and abuse is not a sufficient answer to a diffi- culty of this nature, and we regret that men, like Schuchert, have replied with more anger than logic. The orthodox geol- ogist seems unnecessarily petulant, whenever he is called upon to verify or substantiate the foundational principles of lithic chronology. One frequently hears him make the excuse that "geology has its own peculiar method of proof." To claim ex- emption, however, from the universal criterions of criticism and logic is a subterfuge wholly unworthy of a genuine science, and, if Price insists on discussing a subject, which the ortho- FOSSIL PEDIGREES 99 dox geologist prefers to suppress, it is the latter, and not the former, .who is really reactionary. Price begins by stating the issue in the form of a twofold question: (1) How can we be sure, with respect to a given fauna (or flora) , say the Cambrian, that at one time it monop- olized our globe to the complete exclusion of all other typical faunas (or floras)., say the Devonian, or the Tertiary, of which it is assumed that they could not, by any stretch of imagination, have been contemporaneous, on either land or sea, with the aforesaid "older" fauna (or flora) ? (2) Do the forma- tions (rocks containing fossils) universally occur in such a rigidly invariable order of sequence with respect to one an- other, as to warrant our being sure of the starting-point in the time-scale, or to justify us in projecting any given local order of succession into distant localities, for purposes of chrono- logical correlation? His response to the first of these questions consti- tutes what may be called an aprioristic refutation of the orthodox view, by placing the evolutionary palaeon- tologist in the trilemma: (a) of making the awkward con- fession that, except within limited local areas., he has no means whatever of distinguishing between a geographical distribution of coeval fossil forms among various habitats and a chrono- logical distribution of fossils among sediments deposited at different times; (b) or of denying the possibility of geographi- cal distribution in the past, by claiming dogmatically that the world during Cambrian times, for example, was totally unlike the modern world, of which alone we have experi- mental knowledge, inasmuch as^ it was then destitute of zoological provinces, districts, zones, and other habitats pecu- liar to various types of fauna, so that the whole world formed but one grand habitat, extending over land and sea, for a limited group of organisms made up exclusively of the lower types of life; (c) or of reviving the discredited onion-coat theory of Abraham Werner under a revised biological form, which as- serts that the whole globe is enveloped with fossiliferous rather 100 THE CASE AGAINST EVOLUTION than mineral strata, whose order of succession being every- where the same enables us to discriminate with precision and certainty between cases of distribution in time and cases of distribution in space. In his response to the second question, Professor Price ad- duces numerous factual arguments, which show that the invariable order of sequence postulated by the theory of the time-value of index fossils, not only finds no confirmation in the actual or concrete sequences of fossiliferous rocks, but is often directly contradicted thereby. ''Older" rocks may occur above "younger" rocks, the ''youngest" may occur in immediate succession to the "oldest," Tertiary rocks may be crystalline, consolidated, and "old in appearance," while Cam- brian and even pre-Cambrian rocks sometimes occur in a soft, incoherent condition, that gives them the physical appearance of being as young as Pleistocene formations. These exceptions and objections to the "invariable order" of the fossiliferous strata accumulate from day to day, and it is only by means of Procrustean tactics of the most drastic sort that the facts can be brought into any semblance of harmony with the cur- rent dogmas, which base geology upon evolution rather than evolution upon geology. Price, then, proposes for serious consideration the possi- bility that Cretaceous dinosaurs and even Tertiary mammals may have been living on the land at the same time that the Cambrian graptolites and trilobites were living in the seas. "Who," he exclaims, "will have the hardihood, the real dog- matism to affirm in a serious way that Cambrian animals and seaweeds were for a long time the only forms of life existing anywhere on earth?" Should we, nevertheless, make bold enough to aver that for countless centuries a mere few of the lower forms of life monopolized our globe, as one universal habitat unpartitioned into particular biological provinces or zones, we are thereupon confronted with two equally unwel- come alternatives. We must either fly in the face of experience and legitimate induction by denying the existence in the past of FOSSIL PEDIGREES 101 anything analogous to our present-day geographical distribu- tion of plants and animals into various biological provinces, or be prepared to show by what infallible criterion we are enabled to distinguish between synchronously deposited formations indicative of a geographical distribution according to regional diversity, and consecutively deposited formations indicative of comparative antiquity. The former alternative does not merit any consideration whatever. The latter, as we shall presently see, involves us in an assumption, for which no defense either aprioristic or factual is available. We can, indeed, distinguish between spatial, and temporal, distribution within the narrow limits of a single locality by using the criterion of superposition; for in regions of outcrop, where one sedimentary rock overlies another, the obvious presumption is that the upper rock was deposited at a later date than the lower rock. But the criterion of superposition is not available for the correlation of strata in localities so distant from each other that no physical evidence of stratigraphic continuity is discernible. Moreover the in- duction, which projects any local order of stratigraphical sequence into far distant localities on the sole basis of fossil taxonomy, is logically unsound and leads to conclusions at variance with the actual facts. Hence the alleged time-value of index fossils becomes essentially problematic, and affords no basis whatever for scientific certainty. As previously stated, the sequence of strata is visible only in regions of outcrop, and nowhere are we able to see more than mere parts of two or, at most, three systems associated to- gether in a single locality. Moreover, each set of beds is of limited areal extent, and the limits are frequently visible to the eye of the observer. In any case, their visible extent is necessarily limited. It is impossible, therefore, to correlate the strata of one continent with those of another continent by tracing stratigraphic continuity. Hence, in comparing parti- cular horizons of various ages and in distinguishing them from other horizons over large areas, we are obliged to sub- 102 THE CASE AGAINST EVOLUTION stitute induction for direct observation. Scientific induction, however, is only valid when it rests upon some universal uni- formity or invariable sequence of nature. Hence, to be spe- cific, the assumption that the time-scale based on the European classification of fossiliferous strata is applicable to the entire globe as a whole, is based on the further assumption that we are sure of the universality of fossiliferous stratification over the face of the earth, and that, as a matter of fact, fossils are always and everywhere found in the same order of invariable sequence. But this is tantamount to reviving, under what Spencer calls *'a transcendental form," the exploded ''onion-coat" hypothe- sis of Werner (1749-1817). Werner conceived the terrestrial globe as encircled with successive mineral envelopes, bas- ing his scheme of universal stratification upon that order of sequence among rocks, which he had observed within the narrow confines of his native district in Germany. His hy- pothesis, after leading many scientists astray, was ultimately discredited and laughed out of existence. For it finally be- came evident to all observers that Werner's scheme did not fit the facts, and men were able to witness with their own eyes the simultaneous deposition, in separate localities, of sedi- ments which differed radically in their mineral contents and texture. Thus it came to pass that this classification of strata according to their mineral nature and physical appearance lost all value as an absolute time-scale, while the theory it- self was relegated to the status of a curious and amusing epi- sode in the history of scientific fiascos. Thanks, however, to Wm. Smith and to Cuvier, the dis- carded onion-coat hypothesis did not perish utterly, but was rehabilitated and bequeathed to us in a new and more subtle form. Werner's fundamental idea of the universality of a given kind of deposit was retained, but his mineral strata were re- placed by fossiliferous strata, the lithological onion-coats of Werner being superseded by the biological onion-coats of our modem theory. The geologist of today discounts physical FOSSIL PEDIGREES 103 appearance, and classifies strata according to their fossil, rather than their mineral, contents, but he stands committed to the same old postulate of universal deposits. He has no hesi- tation in synchronizing such widely-scattered formations as the Devonian deposits of New York State, England, Germany, and South America. He pieces them all together as parts of a single system of rocks. He has no misgiving as to the uni- versal applicability of the European scheme of stratigraphic classification, but assures us, in the words of the geologist, Wm. B. Scott, that: ''Even the minuter divisions, the sub- divisions and zones of the European Jura, are applicable to the classification of the South American beds." ("Introduc- tion to Geology," p. 681f.) The limestone and sandstone strata of Werner are now things of the past, but, in their stead, we have, to quote the criticism of Herbert Spencer, "groups of formations which everywhere succeed each other in a given order, and are severally everywhere of the same age. Though it may not be asserted that these successive systems are universal, yet it seems to be tacitly assumed that they are so. . . . Though probably no competent geologist would contend that the European classification of strata is applicable to the globe as a whole, yet most, if not all geol- ogists, write as though it were so. . . . Must we not say that though the onion-coat hypothesis is dead, its spirit is traceable, under a transcendental form, even in the conclu- sions of its antagonists." ("Illustrations of Universal Prog- ress," pp. 329-380, ed. of 1890.) But overlooking, for the moment, the mechanical absurdity involved in the notion of a regular succession of universal layers of sediment, and conceding, for the sake of argument, that the substitution of fossiliferous, for lithological, strata may conceivably have remedied the defects of Werner's geol- ogical time-scale, let us confine ourselves to the one question, which, after all, is of prime importance, whether, namely, without the aid of Procrustean tactics, the actual facts of geology can be brought into alignment with the doctrine of 104 THE CASE AGAINST EVOLUTION an invariable order of succession among fossil types, and its sequel, the intrinsic time-value of index fossils. The question, in other words, is whether or not a reliable time-scale can be based on the facts of fossiliferous stratification as they are observed to exist in the concrete. Price's answer is negative, and he formulates several empirical laws to express the con- crete facts, on which he bases his contention. The laws and facts to which he appeals may be summarized as follows: 1. The concrete facts of geology do not warrant our singling out any fossiliferous deposit as unquestionably the oldest, and hence we have no reliable starting-point for our time-scale, because: (a) We may lay it down as an empirical law that ''any kind of fossiliferous rock (even the 'youngest'), that is, strata belonging to any of the systems or other subdivisions, may rest directly upon the Archaean or primitive crystalline rocks, wit'^out any other so-called 'younger' strata intervening; also these rocks, Permian, Cretaceous, Tertiary, or whatever thus reposing directly on the Archaean may be themselves crystal- line or wholly metamorphic in texture. And this applies not alone to small points of contact, but to large areas." (h) Conversely: any kind of fossiliferous strata (even the "oldest") may not only constitute the surface rocks over wide areas,^ but may consist of loose, unconsolidated materials, thus in both position and texture resembling the "late" Ter- tiaries or the Pleistocene — "In some regions, notably in the Baltic province and in parts of the United States," says John Allen Howe, alluding to the Cambrian rocks around the Baltic * "It is a common occurrence," says Charles Schuchert, ''on the Cana- dian Shield to find the Archseozoic formations overlain by the most recent Pleistocene glacial deposits, and even these may be absent. It appears as if in such places no rocks had been deposited, either by the sea or by the forces of the land, since Archseozoic time, and yet geologists know that the shield has been variously covered by sheets of sediments formed at sundry times in the Proterozoic, Palaeozoic, and, to a more limited extent, in the Mesozoic." C'Text-book of Geology," ed. of 1920, II, p. 569.) It may be remarked that, when geologists "know" such things, they know them in spite of the facts! FOSSIL PEDIGREES 105 Sea and in Wisconsin, "the rocks still retain their original horizontality of deposition, the muds are scarcely indurated, and the sands are incoherent." (Encycl. Brit., vol. V, p. 86.) A large number of striking instances are cited by Price to substantiate the foregoing rule and its converse. The impres- sion left is that not only is the starting-point of the time- scale in doubt, but that, if we were to judge the age of the rocks by their physical appearance and position, we could not accept the conventional verdicts of modern geology, which makes fossil evidence prevail over every other consider- ation. 2. When two contiguous strata are parallel to each other, and there is no indication of disturbance in the lower bed, nor any evidence of erosion along the plane of contact, the two beds are said to exhibit conformity, and this is ordinarily interpreted by geologists as a sign that the upper bed has been laid down in immediate sequence to the lower, and that there has been a substantial continuity of deposition, with no long interval during which the lower bed was exposed as surface to the agents of erosion. When such a conformity exists, as it frequently does, between a "recent" stratum, above, and what is said (according to the testimony of the fossils) to be a very "ancient" stratum, below, and though the two are so alike lithologically as to be mistaken for one and the same formation, nevertheless, such a conformity is termed a "non-evident disconformity," or "deceptive conform- ity," implying that, inasmuch as the "lost interval," repre- senting, perhaps, a lapse of "several million years," is en- tirely unrecorded by any intervening deposition, or any erosion, or any disturbance of the lower bed, we should not have suspected that so great a hiatus had intervened, were it not for the testimony of the fossils. Price cites innumerable ex- amples, and sums them up in the general terms of the fol- lowing empirical law: "Any sort of fossiliferous formation may occur on top of any other 'older' fossiliferous formation, with all the physical evidences of perfect conformity, just 106 THE CASE AGAINST EVOLUTION as if these alleged incongruous or mismated formations had in reality followed one another in quick succession." A quotation from Schuchert's "Textbook of Geology," (1920), may be given by way of illustration: "The imperfec- tion," we read, "of the geologic column is greatest in the interior of North America and more so in the north than in the south. This imperfection is in many places very marked, since an entire period or several periods may be absent. With such great breaks in the local sections the natural assumption is that these gaps are easily seen in the sequence of the strata, but in many places the beds lie in such perfect conformity upon one another that the breaks are not noticeable by the eye and can be proved to exist only by the entombed fossils on each side of a given bedding plane. . . . Stratigraphers are, as a rule, now fully aware of the imperfections in the geologic record, but the rocks of two unrelated formations may rest upon each other w4th such absolute conformability as to be completely deceptive. For instance, in the Bear Grass quarries at Louisville, Ky., a face of limestone is exposed in which the absolute conformability of the beds can be traced for nearly a mile, and yet within 5 feet of vertical thickness is found a Middle Silurian coral bed overlain by another coral zone of Middle Devonian. The parting between these two zones is like that between any two limestone beds, but this insignificant line represents a stratigraphic hiatus the equivalent of the last third of Silurian and the first of De- vonian time. But such disconformities are by no means rare, in fact are very common throughout the wide central basin area of North America." {Op. cit., II, pp. 586-588.) In such cases, the stratigraphical relations give no hint of any enormous gap at the line of contact. On the contrary, there is every evidence of unbroken sequence, and the phys- ical appearances are as if these supposed "geological epochs" had never occurred in the localities, of which there is ques- tion. Everything points to the conclusion that the alleged long intervals of time between such perfectly conformable, and, FOSSIL PEDIGREES 107 often, lithologically identical, formations are a pure fiction elaborated for the purpose of bolstering up the dogma of the universal applicability of the European classification of fos- siliferous rocks. Why not take the facts as we find them? Why resort to tortuous explanations for the mere purpose of saving an arbitrary time-scale? Why insist on a definite time- value for fossils, when it drives us to the extremity of discrediting the objective evidence of physical facts in deference to the preconceptions of orthodox geology? Were it not for theoretical considerations, these stratigraphic facts would be taken at their face value, and the need of saving the reputation of the fossil as an infallible time index is not sufficiently imperative to warrant so drastic a revision of the physical evidence. 3. The third class of facts militating against the time-value of index fossils, are what Price describes as "deceptive con- formities turned upside down," and what orthodox geology tries to explain away as "thrusts," "thrust faults," "over- thrusts," "low-angle faulting," etc.^ In instances of this kind we find the accepted order of the fossiliferous strata reversed in such a way that the "younger" strata are con- formably overlain by "older" strata, and the "older" strata are sometimes interbedded between "younger" strata. "In many places all over the world," says Price, "fossils have been found in a relative order which was formerly thought to be utterly impossible. That is, the fossils have been found in the 'wrong' order, and on such a scale that there can be no mistake about it. For when an area 500 miles long ^ Thus, to explain away "wrong sequences" of fossils, Heim and Rothpletz postulate the great Glaums overthrust in the Alps, Geikie the great overthrust in Scotland, McConnell, Campbell, and Willis a great overthrust along the eastern front of the Rockies in Montana and Alberta, while Hayes recognizes numerous overthrusts in the southern Appalachians. "The deciphering of such great displacements," says Pirrson, speaking of thrust faults, "is one of the greatest triumphs of modem geological research." ("Textbook of Geology," 1920, I, p. 367.) Desperate measures are evidently justifiable, when it is a question of saving the time-value of fossils 1 108 THE CASE AGAINST EVOLUTION and from 20 to 50 miles wide is found with Palaeozoic rocks on top, or composing the mountains, and with Cretaceous beds underneath, or composing the valleys, and running under these mountains all around, as in the case of the Glacier Na- tional Park and the southern part of Alberta, the old notion about the exact and invariable order of the fossils has to be given up entirely." Price formulates his third law as follows : ''Any f ossilif erous formation, 'old' or 'young,' may occur conformably on any other f ossilif erous formation, 'younger' or 'older.' " The corol- lary of this empirical law is that we are no longer justified in regarding any fossils as intrinsically older than other fossils, and that our present classification of fossiliferous strata has a taxonomic, rather than a historical, value. Low-angle faulting is the phenomenon devised by geolo- gists to meet the difficulty of "inverted sequence," when all other explanations fail. Immense mountain masses are said to have been detached from their roots and pushed horizon- tally over the surface (without disturbing it in the least), until they came finally to rest in perfect conformity upon "younger" strata, so that the plane of slippage ended by being indistinguishable from an ordinary horizontal bedding plane. These gigantic "overthrusts" or "thrust faults" are a rather unique phenomenon. Normal faulting is always at a high angle closely approaching the vertical, but "thrust faults" are at a low angle closely approximating the horizontal, and there is enormous displacement along the plane of slippage. The huge mountain masses are said to have been first lifted up and then thrust horizontally for vast distances, sometimes for hundreds of miles, over the face of the land, being thus pushed over on top of "younger" rocks, so as to repose upon the latter in a relation of per- fectly conformable superposition. R. G. McConnell, of the Canadian Survey, comments on the remarkable similarity between these alleged "thrust planes" and ordinary stratifica- tion planes, and he is at a loss to know why the surface soil FOSSIL PEDIGREES 109 was not disturbed by the huge rock masses which slid over it for such great distances. Speaking of the Bow River Gap, he says: "The fault plane here is nearly horizontal, and the two formations, viewed from the valley appear to succeed one another conformably," and then having noted that the under- lying Cretaceous shales are "very soft," he adds that they "have suffered little by the sliding of the limestones over them." (An. Rpt. 1886, part D., pp. 33, 34, 84.) Credat ludaeus Apella, non ego! Schuchert describes the Alpine overthrust as follows: "The movement was both vertical and thrusting from the south and southeast, from the southern portion of Tethys, elevat- ing and folding the Tertiary and older strata of the northern areas of this mediterranean into overturned, recumbent, and nearly horizontal folds, and pushing the southern or Lepontine Alps about 60 miles to the northward into the Helvetic region. Erosion has since carved up these overthrust sheets, leaving remnants lying on foundations which belong to a more north- ern portion of the ancient sea. Most noted of these residuals of overthrust masses is the Matterhorn, a mighty mountain without roots, a stranger in a foreign geologic environment," (Pirsson & Schuchert's "Textbook of Geology," 1920, II, p. 924.) With such a convenient device as the "overthrust" at his disposal, it is hard to see how any possible concrete sequence of fossiliferous strata could contradict the preconceptions of an evolutionary geologist. The hypotheses and assumptions involved, however, are so tortuous and incredible, that nothing short of fanatical devotion to the theory of transformism can render them acceptable. "Examples," says Price, "of strata in the 'wrong' order were first reported from the Alps nearly half a century ago. Since that time, whole armfuls of learned treatises in German, in French, and in English have been written to explain the wonderful conditions there found. The diagrams that have been drawn to account for the strange order of the strata are worthy to rank with the similar ones 110 THE CASE AGAINST EVOLUTION by the Ptolemaic astronomers picturing the cycles and epi- cycles required to explain the peculiar behavior of the heavenly bodies in accordance with the geocentric theory of the universe then prevailing. ... In Scandinavia, a district some 1,120 miles long by 80 miles wide is alleged to have been pushed horizontally eastward 'at least 86 miles.' (Schuchert.) In Northern China, one of these upside down areas is reported by the Carnegie Research Expedition to be 500 miles long." ("The New Geology," 1923, pp. 633, 634.) Nor are the epicyclic subterfuges of the evolutionary geol- ogist confined to "deceptive conformities" and "overthrusts." His inventive genius has hit upon other methods of ex- plaining away inconvenient facts. When, for example, "younger" fossils are found interbedded with "older" fossils, and the discrepancy in time is not too great, he rids himself of the difficulty of their premature appearance by calling them a "pioneer colony." Similarly, when a group of "characteris- tic" fossils occur in one age, skip another "age," and recur in a third, he recognizes the possibility of "recurrent faunas," some of these faunas having as many as five successive "re- currences." Clearly, the assumption of gradual approxima- tion and the dogma that the lower preceded the higher forms of life are things to be saved at all costs, and it is a foregone conclusion that no facts will be suffered to conflict with these irrevisable articles of evolutionary faith. "What is the use," exclaims Price, "of pretending that we are investigating a problem of natural science, if we already know beforehand that the lower and more generalized forms of animals and plants came into existence first, and the higher and the more special- ized came only long afterwards, and that specimens of all these successive types have been pigeonholed in the rocks in order to help us illustrate this wonderful truth?" [Op. cit., pp. 667, 668.) The predominance of extinct species in certain formations is said to be an independent argument of their great age. Most of the species of organisms found as fossils in Cambrian, FOSSIL PEDIGREES 111 Ordovician, and Silurian rocks are extinct, whereas modern types abound in Cretaceous and Tertiary rocks. Hence it is claimed that the former must be vastly older than the latter. But this argument gratuitously assumes the substantial per- fection of the stone record of ancient life and unwarrantedly excludes the possibility of a sudden impoverishment of the world's flora and fauna as the result of a sweeping catastrophe, of which our present species are the fortunate survivors. Now the fact that certain floras and faunas skip entire systems of rocks to reappear only in later formations is proof positive that the record of ancient life is far from being complete, and we have in the abundant fossil remains of tropical plants and animals, found in what are now the frozen arctic regions, unmistakable evidence of a sudden catastrophic change by which a once genial climate "was abruptly terminated. For carcasses of the Siberian elephants were frozen so suddenly and so completely that the flesh has remained untainted." (Dana.) Again, the mere jact of extinction tells us nothing about the time of the extinction. For this we are obliged to fall back on the index fossil whose inherent time-value is based on the theory of evolution and not on stratigraphy. Hence the argument from extinct species is not an independent argument. To sum up, therefore, the aprioristic evolutional series of fossils is not a genuine time-scale. The only safe criterion of comparative age is that of stratigraphic superposition, and this is inapplicable outside of limited local areas. ^ The index fossil is a reliable basis for the chronological correlation of beds only in case one is already convinced on other grounds of the actuality of evolution, but for the unbiased inquirer it is destitute of any inherent time-value. In other words, we can no longer be sure that a given formation is old merely be- cause it happens to contain Cambrian fossils, nor that a rock is young merely because it chances to contain Tertiary fos- '"All that geology can prove," says Huxley, "is local order of suc- cession." ("Discourses Biological and Geological," pp. 279-288.) 112 THE CASE AGAINST EVOLUTION sils. Our present classification of rocks according to their fossil contents is purely arbitrary and artificial, being tanta- mount to nothing more than a mere taxonomical classifica- tion of the forms of ancient life on our globe, irrespective of their comparative antiquity. This scheme of classification is, indeed, universally applicable, and places can usually be found in it for new fossiliferous strata, whenever and wherever dis- covered. Its universal applicability, however, is due not to any prevalent order of invariable sequence among fossilif- erous strata, but solely to the fact that the laws of biological taxonomy and ecology are universal laws which transcend spatial and temporal limitation. If a scheme of taxonomy is truly scientific, all forms of life, whether extant or extinct, will fit into it quite readily. The anomalies of spatial distribution constitute a sixth diffi- culty for transformistic palaeontology. In constructing a phy- logeny the most diverse and widely-separated regions are put under tribute to furnish the requisite fossils, no heed being paid to what are now at any rate impassable geographical barriers, not to speak of the climatic and environmental lim- itations which restrict the migrations of non-cosmopolitan spe- cies within the boundaries of narrow habitats. Hypothetical lineages of a modern form of life are frequently constructed from fossil remains found in two or more continents separated from one another by immense distances and vast oceanic ex- panses. When taxed with failure to plausibleize this proced- ure, the evolutionist meets the difficulty by hypothecating wholesale and devious migrations to and fro, and by raising up alleged land bridges to accommodate plants and animals in their suppositional migrations from one continent to another, etc. The European horse, with his so-called ancestry interred, partly in the Tertiary deposits of Europe, but mostly in those of North America, is a typical instance of these anomalies in geographical distribution. It would, of course, be preposter- ous to suppose that two independent lines of descent could FOSSIL PEDIGREES 113 have fortuitously terminated in the production of one and the same type, namely, the genus Equus. Moreover, to admit for a moment that the extinct American Equus and the extant European Equus had converged by similar stages from distinct origins would be equivalent, as we have seen, to a surrender of the basic postulate that structural similarity rests on the principle of inheritance. Nothing remains, therefore, but to hypothecate a Tertiary land bridge between Europe and North America. ' Modern geologists, however, are beginning to resent these arbitrary interferences with their science in the interest of biological theories. Land bridges, they rightly insist, should be demonstrated by means of positive geological evidence and not by the mere exigencies of a hypothetical genealogy. Who- soever postulates a land bridge between continents should be able to adduce solid reasons, and to assign a mechanism capable of accomplishing the five-mile uplift necessary to bring a deep-sea bottom to the surface of the hydrosphere. Such an idea is extravagant and not to be easily entertained in our day, when geologists are beginning to understand the principle of isostasy. To-day, the crust of the earth, that is, the entire surface of the lithosphere, is conceived as being constituted of earth columns, all of which rest with equal weight upon the level of complete compensation, which exists at a depth of some 76 miles below land surfaces. At this depth viscous flows and undertows of the earth take place, com- pensating all differences of gravitational stress. Hence the materials constituting a mountain column are thought to be less dense than those constituting the surrounding lowland columns, and for this reason the mountains are buoyed up above the surrounding landscape. The columns under ocean bottoms, on the contrary, are thought to consist of heavy materials like basalt, which tend to depress the column. To raise a sea floor, therefore, some means of producing a dilata- tion of these materials would have to be available. Arthur B. Coleman called attention to this difficulty in his Presidential 114 THE CASE AGAINST EVOLUTION Address to the Geological Society of America (December 29, 1915), and we camiot do better than quote his own statement of the matter here: "Admitting," he says, "that in the beginning the litho- sphere bulged up in places, so as to form continents, and sagged in other places, so as to form ocean beds, there are interesting problems presented as to the permanence of land and seas. All will admit marginal changes affecting large areas, but these encroachments of the sea on the continents and the later retreats may be of quite a subordinate kind, not implying an interchange of deep-sea bottoms and land sur- faces. The essential permanence of continents and oceans has been firmly held by many geologists, notably Dana among the older ones, and seems reasonable; but there are geologists, especially palaeontologists, who display great recklessness in rearranging land and sea. The trend of a mountain range, or the convenience of a running bird, or a marsupial afraid to wet his feet seems sufficient warrant for hoisting up any sea bottom to connect continent with continent. A Gondwana Land arises in place of an Indian Ocean and sweeps across to South America, so that a spore-bearing plant can follow up an ice age; or an Atlantis ties New England to Old England to help out the migrations of a shallow-water fauna; or a 'Lost Land of Agulhas' joins South Africa and India. "It is curious to find these revolutionary suggestions made at a time when geodesists are demonstrating that the earth's crust over large areas, and perhaps everywhere, approaches a state of isostatic equilibrium, and that isostatic compensation is probably complete at a depth of only 76 miles" . . . and (having noted the difference of density that must exist be- tween the continental, and submarine, earth columns) Cole- man would have us bear in mind "that to transform great areas of sea bottom into land it would be necessary either to expand the rock beneath by several per cent or to replace heavy rock, such as basalt, by lighter materials, such as gran- ite. There is no obvious way in which the rock beneath a FOSSIL PEDIGREES 115 sea bottom can be expanded enough to lift it 20,000 feet, as would be necessary in parts of the Indian Ocean, to form a Gondwana land; so one must assume that light rocks re- place heavy ones beneath a million square miles of ocean floor. Even with unlimited time, it is hard to imagine a mechanism that could do the work, and no convincing geologi- cal evidence can be brought forward to show that such a thing ever took place. . . . The distribution of plants and animals should be arranged for by other means than by the wholesale elevation of ocean beds to make dry land bridges for them." (Smithson. Inst. Rpt. for 1916, pp. 269-271.) A seventh anomaly of palaeontological phylogeny is what may be described as contrariety of direction. We are asked to believe, for example, that in mammals racial development re- sulted in dimensional increase. The primitive ancestor of mammoths, mastodons, and elephants is alleged to have been the Moeritherium, "a small tapirlike form, from the Middle Eocene Qasr-el-Sagha beds of the Fayum in Egypt. . . . Moeritherium measured about 3V2 feet in height." (Lull: Smithson. Inst. Rpt. for 1908, pp. 655, 656.) The ancestor of the modern horse, we are told, was ''a little animal less than a foot in height, known as Eohippios, from the rocks of the Eocene age." (Woodruff: "Foundations of Biology," p. 361.) In the case of insects, on the other hand, we are asked to believe the exact reverse, namely, that racial development brought about dimensional reduction. "In the middle of the Upper Carboniferous periods," says Anton Handlirsch, "the forest swamps were populated with cockroaches about as long as a finger, dragonfly-like creatures with a wing spread of about 2y2 feet, while insects that resemble our May flies were as big as a hand. ("Die fossilen Insekten, und die Phylogenie der recenten Formen," 1908, L. c, p. 1150.) Contrasting one of these giant palaeozoic dragonflies, Meganeura monyi Brongn., with the largest of modern dragonflies, Aeschna grandis L., Chetverikov exclaims with reference to the latter: "What a pitiful pigmy it is and its specific name (grandis) sounds like 116 THE CASE AGAINST EVOLUTION such a mockery." (Smithson. Inst. Rpt. for 1918, p. 446.) Chetverikov, it is true, proposes a teleological reason for this progressive diminution, but the fact remains that for dysteleo- logical evolutionism, which dispenses with the postulate of a Providential coordination and regulation of natural agencies, this diminuendo of the "evolving" insects stands in irrecon- cilable opposition to the crescendo of the ''evolving" mammals, and constitutes a difficulty which a purely mechanistic philos- ophy can never surmount. Not to prolong excessively this already protracted enumera- tion of discrepancies between fossil fact and evolutionary as- sumption, we shall mention, as an eighth and final difficulty, the indubitable persistence of unchanged organic types from the earliest geological epochs down to the present time. This phenomenon is all the more wonderful in view of the fact that the decision as to which are to be the ''older" and which the "younger" strata rests with the evolutionary geologist, who is naturally disinclined to admit the antiquity of strata contain- ing modern types, and whose position as arbiter enables him to date formations aprioristically, according to the exigencies of the transformistic theory. Using, as he does, the absence of modern types as an express criterion of age, and having, as it were, his pick among the various fossiliferous deposits, one would expect him to be eminently successful in eliminating from the stratigraphic groups selected for senior honors all strata containing fossil types identical with modern forms. Since, however, even the most ingenious sort of geological gerrymandering fails to make this elimination complete, we must conclude that the evidence for persistence of type is in- escapable and valid under any assumption. When we speak of persistent types, we mean generic and specific, rather than phyletic, types, although it is assuredly true that the persistence of the great phyla, from their abrupt and contemporaneous appearance in Cambrian and pre-Cam- brian rocks down to the present day, constitutes a grave difficulty for progressive evolution in general and monophy- FOSSIL PEDIGREES 117 letic evolution in particular. All the great invertebrate types, such as the protozoa, the annelida, the brachiopoda, and large crustaceans called eurypterids, are found in rocks of the Pro- terozoic group, despite the damaged condition of the Archaean record, while in the Cambrian they are represented by a great profusion of forms. "The Lower Cambrian species," says Dana, "have not the simplicity of structure that would natur- ally be looked for in the earliest Palaeozoic life. They are per- fect of their kind and highly specialized structures. No steps from simple kinds leading up to them have been discovered; no line from the protozoans up to corals, echinoderms, or worms, or from either of these groups up to brachiopods, mol- lusks, trilobites, or other crustaceans. This appearance of abruptness in the introduction of Cambrian life is one of the striking facts made known by geology." ("Manual," p. 487.) Thus, as we go backward in time, we find the great organic phyla retaining their identity and showing no tendency to converge towards a common origin in one or a few ancestral types. For this reason, as we shall see presently, geologists are beginning to relegate the evolutionary process to unknown depths below the explored portion of the "geological column." What may lurk in these unfathomed profundities, it is, of course, impossible to say, but, if we are to judge by that part of the column which is actually exposed to view, there is no indication whatever of a steady progression from lower, to higher, degrees of organization, and it takes all the imper- turbable idealism of a scientific doctrinaire to discern in such random, abrupt, and unrelated "origins" any evidence of what Blackwelder styles "a slow ^Dut steady increase in com- plexity of structure and in function." {Science, Jan. 27, 1922, p. 90.) But, while the permanence of phyletic types excludes prog- ress, that of generic and specific types excludes change, and hence it is in the latter phenomenon, especially, that the theory of transformism encounters a formidable difiiculty. Palaeo- botany furnishes numerous examples of the persistence of \m- 118 THE CASE AGAINST EVOLUTION changed plant forms. Ferns identical with the modern genus Marattia occur in rocks of the Palaeozoic group. Cycads in- distinguishable from the extant genera Zamia and Cycas are found in strata belonging to the Triassic system, etc., etc. The same is true of animal types. In all the phyla some genera and even species have persisted unchanged from the oldest strata down to the present day. Among the Protozoa, for example, we have the genus Globigerina (one of the Foram- inifera), some modern species of which are identical with those found in the Cretaceous. To quote the words of the Protozo- ologist, Charles A. Kofoid: 'The Protozoa are found in the oldest fossiliferous rocks and the genera of Radiolaria therein conform rather closely to genera living today, while the fossil Dinoflagellata of the flints of Delitzsch are scarcely distin- guishable from species living in the modern seas. The striking similarities of the most ancient fossil Protozoa to recent ones afford some ground for the inference that the Protozoa living today differ but little from those when life was young." {Science, April 6, 1923, p. 397.) The Metazoa offer similar examples of persistence. Among the Ccelenterata, we have the genus Springopora, whose rep- resentatives from the Carboniferous limestones closely resem- ble some of the present-day reef builders of the East Indies. Species of the brachiopod genera Lingula and Crania occurring in the Cambrian rocks are indistinguishable from species living today, while two other modern genera of the Brachiopoda, namely, Rhynchonella and Disdna, are represented among the fossils found in Mesozoic formations. Terebratulina striata, a fossil species of brachiopod occurring in the rocks belonging to the Cretaceous system, is identical with our modern species Terebratulina caput serpentis. Among the Mollusca such genera as Area, Nucula, Lucina, Astarte, and Nautilus have had a continuous existence since the Silurian, while the genera Lima and Pecten can be traced to the Permian. One genus Pleurotomaria goes back to pre-Cambrian times. As to Ter- tiary fossils, Woods informs us that "in some of the later Cain- FOSSIL PEDIGREES 119 ozoic formations as many as 90 per cent of the species of mollusks are still living." ("Paleontology," 1st ed., p. 2.) Among the Echinodermata, two genera, Cidaris (a sea urchin) and Fentacnnus (a crinoid) may be mentioned as being per- sistent since the Triassic ("oldest" system of the Mesozoic group). Among the Arthropoda, the horseshoe crab Limulus polyphemus has had a continuous existence since the Lias {i.e. the lowest series of the Jurassic system). Even among the Vertebrata we have instances of persistence. The extant Aus- tralian genus Ceratodus, a Dipnoan, has been in existence since the Triassic. Among the fossils of the Jurassic (middle system of the Mesozoic group). Sharks, Rays, and Chimaeroids occur in practically modern forms, while some of the so-called "ganoids" are extremely similar to our present sturgeons and gar pikes — "Some of the Jurassic fishes approximate the tele- osts so closely that it seems arbitrary to call them ganoids." (Scott.) The instances of persistence enumerated above are those ac- knowledged by evolutionary palaeontologists themselves. This list could be extended somewhat by the addition of several other examples, but even so, it would still be small and in- suJSicient to tip the scales decisively in favor of fixism. On the other hand, we must not forget that the paucity of this list is due in large measure to the fact that our present method of classifying fossiliferous strata was deliberately framed with a view to excluding formations containing modern types from the category of "ancient" beds. Moreover, orthodox palaeontology has minimized the facts of persistence to an extent unwarranted even by its own premises. As the follow- ing considerations indicate, the actual number of persistent types is far greater, even according to the evolutionary time- scale, than the figure commonly assigned. First of all, we must take into account the deplorable, if not absolutely dishonest, practice, which is in vogue, of inventing new names for the fossil duplicates of modem species, in order to mask or obscure an identity which conflicts with 120 THE CASE AGAINST EVOLUTION evolutionary preconceptions. When a given formation fails to fit into the accepted scheme by reason of its fossil anachro- nisms, or when, to quote the words of Price, "species are found in kinds of rock where they are not at all expected, and where, according to the prevailing theories, it is quite incredible that they should be found . . . the not very honorable expedient is resorted to of inventing a new name, specific or even generic, to disguise and gloss over the strange similarity between them and the others which have already been assigned to wholly different formations." ("The New Geology," p. 291.) The same observation is made by Heilprin. "It is practically cer- tain," says the latter, "that numerous forms of life, exhibiting no distinctive characters of their own, are constituted into distinct species for no other reason than that they occur in formations widely separated from those holding their nearest kin." ("Geographical and Geological Distribution of Animals," pp. 183, 184.) An instance of this practice occurs in the fore- going list, where a fossil brachiopod identical with a modern species receives the new specific name ''striata.'^ Its influence is also manifest in the previously quoted apology of Scott for calling teleost-like fish "ganoids." We must also take into account the imperfection of the fos- sil record, which is proved by the fact that most of the ac- knowledged "persistent types" listed above "skip" whole systems and even groups of "later" rocks (which are said to represent enormous intervals of time), only to reappear, at last, in modem times. It is evident that their existence has been continuous, and yet they are not represented in the inter- vening strata. Clearly, then, the fossil record is imperfect, and we must conclude that many of our modern types actually did exist in the remote past, without, however, leaving behind any vestige of their former presence. Again, we must frankly confess our profound ignorance with respect to the total number and kinds of species living in our modern seas. Hence our conventional distinction between "ex- tinct" and "extant" species has only a provisory value. Future FOSSIL PEDIGREES 121 discoveries will unquestionably force us to admit that many of the -species now classed as ''extinct" are in reality living forms, which must be added to our list of "persistent types." "It is by no means improbable," says Heilprin, "that many of the older genera, now recognized as distinct by reason of our imperfect knowledge concerning their true relationships, have in reality representatives in the modern sea." {Op. cit. pp. 203, 204.) Finally, the whole of our present taxonomy of plants and animals, both living and fossil, stands badly in need of revision. Systematists, as we have seen in the second chapter, base their classifications mainly on what they regard as basic or homologous structures, in contradistinction to superficial or adaptive characters. Both kinds of structure, however, are purely somatic, and somatic characters, as previously ob- served, are not, by themselves, a safe criterion for discrim- inating between varieties and species. In the light of recent genetical research, we cannot avoid recognizing that there has been far too much "splitting" of organic groups on the basis of differences that are purely fiuctuational, or, at most, muta- tional. Moreover, the distinction between homologous and adaptive structures is often arbitrary and largely a matter of personal opinion, especially when numerous specimens are not available. What the "Cambridge Natural History" says in allusion to the Asteroidea is of general application. "While there is considerable agreement," we read, "amongst author- ities as to the number of families, or minor divisions of un- equivocal relationship, to be found in the class Asteroidea, there has been great uncertainty- both as to the number and limits of the orders into which the class should be divided, and also as to the limits of the various species. The difficulty about the species is by no means confined to the group Echinodermata ; in all cases where the attempt is made to determine species by an examination of a few speci- mens of unknown age there is bound to be uncertainty; the more so, as it becomes increasingly evident that there is no 122 THE CASE AGAINST EVOLUTION sharp line to be drawn between local varieties and species. In Echinodermata, however, there is the additional difficulty that the acquisition of ripe genital cells does not necessarily mark the termination of growth; the animals can continue to grow and at the same time slightly alter their characters. For this reason many of the species described may be merely immature forms. . . . "The disputes, however, as to the number of orders included in the Asteroidea proceed from a different cause. The at- tempt to construct detailed phylogenies involves the assump- tion that one set of structures, which we take as the mark of the class, has remained constant, whilst the others which are regarded as adaptive, may have developed twice or thrice. As the two sets of structures are about of equal importance it will be seen to what an enormous extent the personal equa- tion enters in the determination of these questions." {Op. cit., vol. I, pp. 459, 460.) In dealing with fossil forms, these difficulties of the taxono- mist are intensified: (1) by the sparse, badly-preserved, and fragmentary character of fossil remains; (2) by the fact that here breeding experiments are impossible, and hence the diag- nosis based on external characters cannot be supplemented by a diagnosis of the germinal factors. Fossil taxonomy is, in consequence, extremely arbitrary and unreliable. Many fossil forms classed as distinct species, or even as distinct genera, may be nothing more than fluctuants, mutants, hybrids, or im- mature stages of well-known species living today. Again, many fossils mistaken for distinct species are but different stages in the life-history of a single species, a mistake, which is unavoidable, when specimens are few and the age of the speci- mens unknown. The great confusion engendered in the classi- fication of the hydrozoa by nineteenth-century ignorance of the alternation of hydroid and medusoid generations is a standing example of the danger of classifying forms without a complete knowledge of the entire life-cycle. When due allowance is made for mutation, hybridization, metagenesis, polymorphism, FOSSIL PEDIGREES 123 age and metamorphosis, the number of distinct fossil species will undergo considerable shrinkage. Nor must we overlook the possibility of environmentally-induced modifications. Many organisms, such as mollusks, undergo profound altera- tion as a result of some important, and, perhaps, relatively permanent, change in their environmental conditions, though such alterations affect only the phenotype, and do not involve a corresponding change in the specific genotype, i.e, the germinal constitution of the race. In the degree that these considerations are taken into ac- count the number of "extinct" fossil species will diminish and the number of "persistent" species will increase. This is a con- summation devoutly to be wished for, but it means that hundreds of thousands of described species must needs be reviewed for the purpose of weeding out the dupli- cates, and who will have the knowledge, the courage, or even the span of life, necessary to accomplish so gigantic a task? But so far as the practical purposes of our argument are con- cerned, the accepted list of persistent types needs no ampli- fication. It suffices, as it stands, to establish the central fact (which, for the rest, is admitted by everyone) that some gen- eric and even specific types have remained unchanged through- out the enormous lapse of time which has intervened between the deposition of the oldest strata and the advent of the present age. Our current theories, far from diminishing the significance of this fact, tend to intensify it by computing the duration of such persistence in millions, rather than in thousands, of years. Now, whatever one's views may be on the subject of transformism, this prolonged permanence of certain genera and species is an indubitable fact, which is utterly irreconcilable with a universal law of organic evolution. The theory of transformism is impotent to explain an exception so palpable as this ; for persistence and transmutation cannot be subsumed under one and the same principle. That which accounts for change cannot account for unchange. Yet unchange is an observed fact, while the change, in this case, is an inferred 124 THE CASE AGAINST EVOLUTION hypothesis. Hence, even if we accept the principle of trans- formism, there will always be scope for the principle of per- manence. The extraordinary tenacity of type manifested by persistent genera and species is a phenomenon deserving of far more careful study and investigation than the evolution- ally-minded scientist of to-day deigns to bestow upon it. To the latter it may seem of little consequence, but, to the genuine scientist, the actual persistence of types should be of no less interest than their possible variability. With these reflections, our criticism of the palaeontological argument terminates. The enumeration of its various defi- ciencies was not intended as a refutation. To disprove the theory of organic evolution is a feat beyond our power to accomplish. We can only adduce negative evidence, whose scope is to show that the various evolutionary arguments are inconsequential or inconclusive. We cannot rob the theory of its intrinsic possibility, and sheer justice compels us to con- fess that certain facts, like those of symbiotic preadaptation, lend themselves more readily to a transformistic, than to a fixistic, interpretation. On the other hand, nothing is gained by ignoring flaws so obvious and glaring as those which mar the cogency of palaeontological ''evidence." The man who would gloss them over is no true friend either of Science or of the scientific theory of Evolution ! They represent so many real problems to be frankly faced and fully solved, before the palseontological argument can become a genuine demonstration. But until such time as a demonstration of this sort is forth- coming, the evolutionist must not presume to cram his un- substantiated theory down our reasonably reluctant throats. To accept as certain what remains unproved, is to compromise our intellectual sincerity. True certainty, which rests on the recognition of objective necessity, will never be attainable so long as difficulties that sap the very base of evolutionary ar- gumentation are left unanswered; and, as for those who, in the teeth of discordant factual evidence, profess, nevertheless, to have certainty regarding the "fact" of evolution, we can FOSSIL PEDIGREES 125 only say that such persons cannot have a very high or exact- ing conception of what scientific certainty really means. For the rest, it cannot even be said that the palaeontological record furnishes good circumstantial evidence that our globe has been the scene of a process of organic evolution. In fact, so utterly at variance with this view is the total impression conveyed by the visible portion of the geological column, that the modern geologist proposes, as we have seen, to probe depths beneath its lowest strata for traces of that alleged transmutation, which higher horizons do not reveal. There are six to eight thick terranes below the Cambrian, we are told, and igneous masses that were formerly supposed to be basal have turned out to be intrusions into sedimentary accumula- tions, all of which, of course, is fortunate for the theory of organic evolution, as furnishing it with a sadly needed new court of appeal. The bottom, so to speak, has dropped out of the geological column, and Prof. T. C. Chamberlin announces the fact as follows: ''The sharp division into two parts, a life- less igneous base and a sedimentary fossiliferous superstruc- ture, has given place to the general concept of continuity with merely minor oscillations in times and regions of major activ- ity. Life has been traced much below the Cambrian, but its record is very imperfect. The recent discoveries of more ample and varied life in the lower Palaeozoic, particularly the Cam- brian, implies, under current evolutional philosophy, a very great downward extension of life. In the judgment of some biologists and geologists, this extension probably reaches below all the pre-Cambrian terranes as yet recognized, though this pre-Cambrian extension is great. ^ The 'Azoic' bottom has re- tired to depths unknown. This profoundly changes the life aspect of the 'column.' " {Science, Feb. 8, 1924, p. 128.) All this is doubtless true, but such an appeal, from the known to the unknown, from the actual to the possible, is not far-removed from a confession of scientific insolvency. Life must, of course, have had an earlier history than that recorded in the pre- Cambrian rocks. But even supposing that some portion of an 126 THE CASE AGAINST EVOLUTION earlier record should become accessible to us, it could not be expected to throw much light on the problem of organic origins. Most of the primordial sediments have long since been sapped and engulfed by fiery magmas, while terranes less deep have, in all probability, been so metamorphosed that every trace of their fossil contents has perished. The sub- Archaean beginnings of life will thus remain shrouded for- ever in a mystery, which we have no prospect of penetrating. Hence it is the exposed portion of the geological column which continues and will continue to be our sole source of informa- tion, and it is preeminently on this basis that the evolutionary issue will have to be decided. Yet what could be more enigmatic than the rock record as it stands? For in nature it possesses none of that idealized integrity and coherence, with which geology has invested it for the purpose of making it understandable. Rather it is a mighty chaos of scattered and fragmentary fossiliferous forma- tions, whose baffling complexity, discontinuity, and ambiguity tax the ingenuity of the most sagacious interpreters. Trans- formism is the key to one possible synthesis, which might serve to unify that intricate mass of facts, but it is idle to pretend that this theory is the unique and necessary corollary of the facts as we find them. The palaeontological argument is simply a theoretical construction which presupposes evolu- tion instead of proving it. Its classic pedigrees of the horse, the camel, and the elephant are only credible when we have assumed the "fact" of evolution, and even then, solely upon con- dition that they claim to approximate, rather than assign, the actual ancestry of the animals in question. In palaeontology, as in the field of zoology, evolution is not a conclusion, but an interpretation. In palaeontology, otherwise than in the field of genetics, evolution is not amenable to the check of experi- mental tests, because here it deals not with that which is, but with that which was. Here the sole objective basis is the mu- tilated and partially obliterated record of a march of events, which no one has observed and which will never be repeated. FOSSIL PEDIGREES 127 These obscure and fragmentary vestiges of a vanished past, by reason of their very incompleteness, lend themselves quite readil^^ to all sorts of theories and all sorts of speculations. Of the ''Stone Book of the Universe" we may say with truth that which Oliver Wendell Holmes says of the privately-in- terpreted Bible, namely, that its readers take from it the same views which they had previously brought to it. "I am, hew- ever, thoroughly persuaded," say the late Yves Delage, "that one is or is not a transformist, not so much for reasons de- duced from natural history, as for motives based on personal philosophic opinions. If there existed some other scientific hypothesis besides that of descent to explain the origin of species, many transformists would abandon their present opin- ion as not being sufficiently demonstrated. ... If one takes his stand upon the exclusive ground of the facts, it must be acknowledged that the formation of one species from another species has not been demonstrated at all." ("L'heredite et les grands problemes de la biologic generale," Paris, 1903, pp. 204, 322.) PART II THE PROBLEM OF ORIGINS II THE PROBLEM OF ORIGINS CHAPTER I THE ORIGIN OF LIFE § 1. The Theory of Spontaneous Generation Strictly speaking, the theory of Transformism is not con- cerned with the initial production of organic species, but rather with the subsequent differentiation and multiplication of such species by transmutation of the original forms. This tech- nical sense, however, is embalmed only in the term trans- formism and not in its synonym evolution. The signification of the latter term is less definite. It may be used to denote any sort of development or origination of one thing from another. Hence the problem of the formation of organic species is frequently merged with the problem of the transfor- mation of species under the common title of evolution. This extension of the evolutionary concept, in its widest sense, to the problem of the origin of life on our globe is known as the hypothesis of abiogenesis or spontaneous generation. It regards inorganic matter as the source of organic life not merely in the sense of a passive cause, out of which the pri- mordial forms of life were produced, but in the sense of an active cause inasmuch as it ascribes the origin of life to the exclusive agency of dynamic principles inherent in inor- ganic matter, namely, the physicochemical energies that are native to mineral matter. Life, in other words, is assumed to have arisen spontaneously, that is, by means of a syntl^esis 131 132 THE CASE AGAINST EVOLUTION and convergence of forces resident in inorganic matter, and not through the intervention of any exterior agency. The protagonists of spontaneous ■ generation, therefore, as- sert not merely a passive, but an active, evolution of living, from lifeless matter. As to the fact of the origin of the primal organisms from inorganic matter, there is no controversy whatever. All agree that, at some time or other, the primordial plants and animals emanated from inorganic matter. The sole point of dispute is whether they arose from inorganic matter by active evolution or simply by passive evolution. The pas- sive evolution of mineral matter into plants and animals is an everyday occurrence. The grass assimilates the nitrates of the soil, and is, in turn, assimilated by the sheep, whose flesh be- comes the food of man, and mineral substance is thus finally transformed into human substance. In the course of met- abolic processes, the inorganic molecule may doff its mineral type and don, in succession, the specificities of plant, animal, and human protoplasm; and this transition from lower to higher degrees of perfection may be termed an evolution. It is an ascent of matter from the lowermost grade of an inert substance, through the intermediate grades of vegetative and animal life, up to the culminating and ultimate term of ma- terial perfection, in the partial constitution of a human nature and personality, in the concurrence asi a coagent in vegetative and sensile functions, and in the indirect participation, as in- strument, in the higher psychic functions of rational thought and volition. At the present time, the inorganic world is clearly the ex- clusive source of all the matter found in living beings. All living beings construct their bodies out of inorganic sub- stances in the process of nutrition, and render back to the inorganic world, by dissimilation and death, whatever they have taken from it. We must conclude, therefore, the matter of the primordial organisms was likewise derived from the inorganic world. But we are not warranted in concluding that this process of derivation was an active evolution. On the THE ORIGIN OF LIFE 133 contrary, all evidence is against the supposition that brute matter is able to evolve of itself into living matter. It can, indeed, be transformed into plants, animals, and men through the action of an appropriate external agent (i.e. solely through the agency of the living organism), but it cannot acquire the perfections of living matter by means of its own inherent powers. It cannot vitalize, or sensitize, itself through the un- aided activity of its own physicochemical energies. Only when it comes under the superior influence of preexistent life can it ascend to higher degrees of entitive perfection. It does not become of itself life, sensibility, and intelligence. It must first be drawn into communion with what is already alive, before it can acquire life and sensibility, or share indirectly in the honors of intelligence (as the substrate of the cerebral imagery whence the human mind abstracts its conceptual thought). Apart from this unique influence, inorganic mat- ter is impotent to raise itself in the scale of existence, but, if captured, molded, and transmuted by a living being, it may progress to the point of forming with the human soul one single nature, one single substance, one single person. The evolution of matter exemplified in organic metabolism is ob- viously passive, and such an evolution of the primal organ- isms out of non-living matter even the opponents of the hy- pothesis of spontaneous generation concede. But spontaneous generation implies an active evolution of the living from the lifeless, and this is the point around which the controversy wages. It would, of course, be utterly irrational to deny to the Supreme Lord and Author of Life the power of vivifying matter previously inanimate and inert, and hence the origin of organic life from inorganic matter by a formative (not creative) act of the Creator is the conclusion to which the denial of abiogenesis logically leads. The hypothesis of spontaneous generation is far older than the theory of transformism. It goes back to the Greek prede- cessors of Aristotle, at least, and may be of far greater antiq- uity. It was based, as is well known, upon an erroneous 134 THE CASE AGAINST EVOLUTION interpretation of natural facts, which was universally accepted up to the close of the 17th century. As we can do no more than recount a few outstanding incidents of its long and in- teresting history here, the reader is referred to the VII chapter of Wasmann's "Modern Biology" and the VIII chapter of Windle's ^'Vitalism and Scholasticism" for the details which we are obliged to omit. § 2. The Law of Genetic Continuity From time immemorial the sudden appearance of maggots in putrescent meat had been a matter of common knowledge, and the ancients were misled into regarding the phenomenon as an instance of a de novo origin of life from dead matter. The error in question persisted until the year 1698, when it was decisively disproved by a simple experiment of the Italian physician Francesco Redi. He protected the meat from flies by means of gauze. Under these conditions, no maggots ap- peared in the meat, while the flies, unable to reach the meat, deposited their eggs on the gauze. Thus it became apparent that the maggots were larval flies, which emerged from fer- tilized eggs previously deposited in decaying meat by female flies. Antonio Vallisnieri, another Italian, showed that the fruit-fly had a similar life-history. As a result of these dis- coveries, Redi rejected the theory of spontaneous generation and formulated the first article of the Law of Genetic Vital Continuity: Omne vivum ex vivo. Meanwhile, the first researches conducted by means of the newly invented compound microscope disclosed what appeared to be fresh evidence in favor of the discarded hypothesis. The unicellular organisms known as infusoria were found to ap- pear suddenly in hay infusions, and their abrupt appearance was ascribed to spontaneous generation. Towards the end of the 18th century, however, a Catholic priest named Lazzaro Spallanzani refuted this new argument by sterilizing the infu- sions with heat and by sealing the containers as protection against contamination by floating spores or cysts. After the THE ORIGIN OF LIFE 135 infusions had been boiled for a sufficient time and then sealed, no organisms could be found in them, no matter how long they were kept. We now know that protozoa and protophytes do not originate de novo in infusions. Their sudden appearance in cultures is due to the deposition of spores or cysts from the air, etc. The possibility that the non-germination of life in sterilized infusions kept in sealed containers might be due to the absence of oxygen, removed by boiling and excluded by sealing, left open a single loophole, of which the 19th century defenders of abiogenesis proceeded to avail themselves. Pasteur, how- ever, by employing sterilized cultures, which he aerated with filtered air exclusively, succeeded in depriving his opponents of this final refuge, and thereby completely demolished the last piece of evidence in favor of spontaneous generation. Prof. Wm. Sydney Thayer, in an address delivered at the Sor- bonne. May 22, 1923, gives the following account of Pasteur's experiments in this field: "Then, naturally (1860-1876) came the famous studies on spontaneous generation undertaken against the advice of his doubting masters, Biot and Dumas. On the basis of careful and well-conceived experiments he demonstrated the universal presence of bacteria in air, water, dust; he showed the variation in different regions of the bacterial content of the air; he demonstrated the permanent sterility of media protected from contamination, and he in- sisted on the inevitable derivation of every living organism from one of its kind. 'No,' he said, 'there is no circumstance known today which justifies us in affirming that microscopic organisms have come into the world, without parents like themselves. Those who made this assertion have been the playthings of illusions or ill-made experiments invalidated by errors which they have not been able to appreciate or to avoid.' In the course of these experiments he demonstrated the necessity of reliable methods of sterilization for instru- ments or culture media, of exposure for half an hour to moist heat at 120° or to dry air at 180°. And behold! our modem 136 THE CASE AGAINST EVOLUTION procedures of sterilization and the basis of antiseptic surgery." {Science, Dec. 14, 1923, p. 477.) Pasteur brought to a suc- cessful completion the work of Redi and Spallanzani. Hence- forth spontaneous generation was deprived of all countenance in the realm of biological fact. Meanwhile, the cytologists and embryologists of the last century were adding article after article to the law of genetic cellular continuity, thus forging link by link the fatal chain of severance that inexorably debars abiogenesis from the domain of natural science. With the formulation of the great Cell Theory by Schleiden and Schwann (1838-1839), it became clear that the cell is the fundamental unit of organization in the world of living matter. It has proved to be, at once, the simplest organism capable of independent existence and the basic unit of structure and function in all the more complex forms of life. The protists (unicellular protozoans and proto- phytes) consist each of a single cell, and no simpler type of organism is known to science. The cell is the building brick out of which the higher organisms or metists (i.e. the multi- cellular and tissued metazoans and metaphytes) are con- structed, and all multicellular organisms are, at one time or other in their career, reduced to the simplicity of a single cell {v.g. in the zygote and spore stages). The somatic or tissue cells, which are associated in the metists to form one organic whole, are of the same essential type as germ cells and unicellular organisms, although the parallelism is more close between the unicellular organism and the germ cell. The germ cell, like the protist, is equipped with all the poten- tialities of life, whereas tissue cells are specialized for one function rather than another. The protist is a generalized and physiologically-balanced cell, one which performs all the vital functions, and in which the suppression of one function leads to the destruction of all the rest; while the tissue cell is a specialized and physiologically-unbalanced cell limited to a single function, with the other vital functions in abeyance (though capable of manifesting themselves under certain cir- THE ORIGIN OF LIFE 137 cumstances). Normally, therefore, the tissue cell is function- ally incomplete, a part and not a whole, whereas the protist is an independent individual, being, at once, the highest type of cell and the lowest type of organism. According to the classic definition of Franz Leydig and Max Schultze, the cell is a mass of protoplasm containing a nucleus, both protoplasm and nucleus arising through division of the corresponding elements of a preexistent cell. In this form the definition is quite general and applies to all cells, whether tissue cells, germ cells, or unicellular organisms. Moreover, it embodies two principles which still further determine the law of genetic cellular continuity, namely: Omnis cellula ex cellula, enunciated by Virchow in 1855, and Flemming's principle: Omnis nucleus ex nucleo, proclaimed in 1882. In this way, Cytology supplemented Redi's formula that every living being is from a preexistent living being, by adding two more ar- ticles, namely, that every living cell is from a preexistent cell, and every new cellular nucleus is derived by division from a preexistent cellular nucleus. Now neither the nucleus nor the cell-body (the cytoplasm or extranuclear area of the cell) is capable of an independent existence. The cytoplasm of the severed nerve fibre, when it fails to reestablish its connection with the neuron nucleus, degenerates. The enucleated amceba, though capable of such vital functions as depend upon destruc- tive metabolism, can do nothing which involves constructive metabolism, and is, therefore, doomed to perish. The sperm cell, which is a nucleus that has sloughed off most of its cyto- plasm, disintegrates, unless it regains a haven in the cytoplasm of the egg. Life, accordingly, cannot subsist in a unit more simply organized than the cell. No organism lives which is simpler than the cell, and the origin of all higher forms of life is reducible, as we shall see, to the origin of the cell. Conse- quently, new life can originate in no other way than by a process of cell-division. All generation or reproduction of new life is dependent upon the division of the cell-body and nucleus of a preexistent living cell. 138 THE CASE AGAINST EVOLUTION Haeckel, it is true, has attempted to question the status of the cell as the simplest of organisms, by alleging the exist- ence of cytodes (non-nucleated cells) among the bacteria and the blue-green algae. Further study, however, has shown that bacteria and blue-green algae have a distributed nucleus, like that of certain ciliates, such as Dileptus gigas and Trachelo- cerca. In such forms the entire cell body is filled with scat- tered granules of chromatin called chromioles, and this diffuse type of nucleus seems to be the counterpart of the concentrated nuclei found in the generality of cells. At any rate, there is a temporary aggregation of the chromioles at critical stages in the life-cycle (such as cell-division), and these scattered chromatin granules undergo division, although their distribu- tion to the daughter-cells is not as regular as that obtaining in mitosis. All this is strongly suggestive of their nuclear na- ture, and cells with distributed nuclei cannot, therefore, be classified as cytodes. In fact, the polynuclear condition is by no means uncommon. Paramoecium aurelia, for example, has a macronucleus and a micronucleus, and the Uroleptus mohilis has eight macronuclei and from two to four micronuclei. The difference between the polynuclear and diffuse condition seems to be relatively unimportant. In fact, the distributed nucleus differs from the morphological nucleus mainly in the absence of a confining membrane. From the functional standpoint, the two structures are identical. Hence the possession of a nucleus or its equivalent is, to all appearances, a universal characteristic of cells. Haeckel's ''cytodes" have proved to be purely imag- inary entities. The verdict of modern cytologists is that Shultze's definition of the cell must stand, and that the status of the cell as the simplest of organic units capable of inde- pendent existence is established beyond the possibility of prudent doubt. With the progressive refinement of microscopic technique, it has become apparent that the law of genetic continuity ap- plies not merely to the cell as a whole and to its major parts, the nucleus and the cell-body, but also to the minor com- THE ORIGIN OF LIFE 139 ponents or organelles, which are seen to be individually self- perpetuating by means of growth and division. The typical cell nucleus, as is well known, is a spherical vesicle containing a semisolid, diphasic network of basichromatin (formerly "chromatin") and oxychromatin (linin) suspended in more fluid medium or ground called nuclear sap. When the cell is about to divide, the basichromatin resolves itself into a defi- nite number of short threads called chromosomes. Now, Boveri found that, in the normal process of cell-division known as mitosis, these nuclear threads or chromosomes are each split lengthwise and divided into two exactly equivalent halves, the resulting halves being distributed in equal number to the two daughter-cells produced by the division of the original cell. Hence, in the year 1903, Boveri added a fourth article to the law of genetic vital continuity, namely: Omne chromo- soma ex chromosomate. But the law in question applies to cytoplasmic as well as nuclear components. In physical appearance, the cell-body or cytoplasm resembles an emulsion with a clear semiliquid ex- ternal phase called hyaloplasm and an internal phase consist- ing mainly of large spheres called macrosomes and minute particles called microsomes, all of which, together with numerous other formed bodies, are suspended in the clear hyaloplasm (hyaline ground-substance). Now certain of these cytoplasmic components have long been known to be self-perpeticating by means of growth and division, main- taining their continuity from cell to cell. The plas- tids of plant cells, for example, divide at the time of cell- division, although their distribution to the daughter-cells does not appear to be as definite and regular as that which obtains in the case of the chromosomes. Similarly, the centrioles or division-foci of animal cells are self-propagating by division, but here the distribution to the daughter-cells is exactly equiva- lent and not at random as in the case of plastids. In the light of recent research it looks as though two other types of cytoplasmic organelles must be added to the list of cellular 140 THE CASE AGAINST EVOLUTION components, which are individually self-perpetuating by growth and division, namely, the chondriosomes and the Golgi bodies — "both mitochondria and Golgi bodies are able to assimilate, grow, and divide in the cytoplasm." (Gatenby.) Wilson is of opinion that the law of genetic continuity may have to be extended even to those minute granules and par- ticles of the cytosome, which were formerly thought to arise de novo in the apparently structureless hyaloplasm. Speaking of the emulsified appearance of the starfish and sea urchin eggs, he tells us that their protoplasm shows ''a structure some- what like that of an emulsion, consisting of innumerable spheroidal bodies suspended in a clear continuous basis or hyaloplasm. These bodies are of two general orders of mag- nitude, namely: larger spheres or macrosomes rather closely crowded and fairly uniform in size, and much smaller micro- somes irregularly scattered between the macrosomes, and among these are still smaller granules that graduate in size down to the limit of vision with any power {i.e. of micro- scope) we may employ." {Science, March 9, 1923, p. 282.) Now, the limit of microscopic vision by the use of the highest- power oil-immersion objectives is one-half the length of the shortest waves of visible light, that is, about 200 submicrons (the submicron being one millionth of a millimeter). Par- ticles whose diameter is less than this cannot reflect a wave of light, and are, therefore, invisible so far as the micro- scope is concerned. By the aid of the ultramicroscope, how- ever, we are enabled to see the halos formed by particles not more than four submicrons in diameter, which, however, repre- sents the limit of the ultramicroscope, and is the diameter hy- pothetically assigned to the protein multimolecule. Since, therefore, we find the particles in the protoplasm of the cell body graduating all the way down to the limit of this latter instrument, and since on the very limit of microscopic vision we find such minute particles as the centrioles "capable of self-perpetuation by growth and division, and of enlargement to form much larger bodies," we cannot ignore the possibility THE ORIGIN OF LIFE 141 that the ultramicroscopic particles may have the same powers and may be the sources or '^ formative foci" of the larger formed bodies, which were hitherto thought to arise de novo. Certainly, pathology, as we shall see, tells us of ultramicro- scopic disease-germs, which are capable of reproduction and maintenance of a specific type, and experimental genetics makes us aware of a linear alignment of submicroscopic genes in the nuclear chromosomes, each gene undergoing peri- odic division and perpetual transmission from generation to generation. The cytologist, therefore, to quote the words of Wilson, "cannot resist the evidence that the appearance of a simple homogeneous colloidal substance is deceptive; that it is in reality a complex, heterogeneous, or polyphasic sys- tem. He finds it difficult to escape the conclusion, there- fore, that the visible and the invisible components of the protoplasmic system differ only in their size and degree of dispersion; that they belong to a single continuous series, and that the visible structure of protoplasm may give us a rough magnified picture of the invisible." {Ibidem, p. 283.) It would seem, therefore, that we must restore to honor, as the fifth article of the law of cellular continuity, the formula, which Richard Altmann enunciated on purely speculative grounds in 1892, but which the latest research is beginning to place on a solid factual basis, namely: Omne granulum ex granulo. 'Tor my part," says the great cytologist, Wilson, "I am disposed to accept the probability that many of these parti- cles, as if they were submicroscopical plastids, may have a persistent identity, perpetuating themselves by growth and multiplication without loss of their specific individual type." And he adds that the facts revealed by experimental em- bryology {e.g., the existence of differentiated zones of spe- cific composition in the cytoplasm of certain eggs) "drive us to the conclusion that the submicroscopical components of the hyaloplasm are segregated and distributed according to an ordered system." {Ibidem, p. 283.) The structure of the cell has often been likened to a heterogeneous solution, 142 THE CASE AGAINST EVOLUTION that is, to a complex polyphasic colloidal system, but this power of perpetual division and orderly assortment pos- sessed by the cell as a whole and by its single components is the unique property of the living protoplasmic system, and is never found in any of the colloidal systems known to physical chemistry, be they organic or inorganic. Cells, then, originate solely by division of preexistent cells and even the minor components of the cellular system origi- nate in like fashion, namely: by division of their respective counterparts in the preexistent living cell. Here we have the sum and substance of the fivefold law of genetic con- tinuity, whose promulgation has relegated the hypothesis of spontaneous generation to the realms of empty speculation. Waiving the possibility of an a 'priori argument, by which abiogenesis might be positively excluded, there remains this one consideration, which alone is scientifically significant, that, so far as observation goes and induction can carry us, the living cell has absolute need of a vital origin and can never originate by the exclusive agency of the physico- chemical forces native to inorganic matter. If organic life exists in simpler terms than the cell, science knows nothing of it, and no observed process, simple or complicated, of inorganic nature, nor any artificial synthesis of the labora- tory, however ingenious, has ever succeeded in duplicating the wonders of the simplest living cell. § 3. Chemical Theories of the Ori^n of Life In fact, the very notion of a chemical synthesis of living matter is founded on a misconception. It would, indeed, be rash to set limits to the chemist's power of synthesizing organic compounds, but living protoplasm is not a single chemical compound. Rather it is a complex system of com- pounds, enzymes and organelles, coordinated and integrated into an organized whole by a persistent principle of unity and finality. Organic life, to say nothing at all of its unique dynamics^ is a morphological as well as a chemical problem; THE ORIGIN OF LIFE 143 and, while it is conceivable that the chemist might syn- thesize all the compounds found in dead protoplasm, to reproduce a single detail of the ultramicroscopic structure of a living cell lies wholly beyond his power and province. "Long ago," says Wilson (in the already quoted address on the "Physical Basis of Life"), "it became perfectly plain that what we call protoplasm is not chemically a single substance. It is a mixture of many substances, a mixture in high degree complex, the seat of varied and incessant transformations, yet one which somehow holds fast for countless generations to its own specific type. The evidence from every source demonstrates that the cell is a complex organism, a micro- cosm, a living system." {Science, March 9, 1923, p. 278.) With the chemist, analysis must precede synthesis, and it is only after a structural formula has been determined by means of quantitative analysis supplemented by analogy and comparison, that a given compound can be successfully synthesized. But living protoplasm and its structures elude such analysis. Intravitous staining is inadequate even as a means of qualitative analysis, and tests of a more drastic nature destroy the life and organization, which they seek to analyze. "With one span," says Ame Pictet, Professor of Chemistry at the University of Geneva, "we will now bridge the entire distance separating the first products of plant assimilation from its final product, namely, living matter. And it should be understood at the outset that I employ this term 'living matter' only as an abbreviation, and to avoid long circumlocution. You should not, in reality, attribute life to matter itself; it has not, it cannot have both living molecules and dead molecules. Life requires an or- ganization, which is that of cellular structure, but it remains, in contradistinction to it, outside the domain of strict chem- istry. It is none the less true that the content of a living cell must differ in its chemical nature from the content of a dead cell. It is entirely from this point of view that the phenomenon of life pertains to my subject. ... A living 144 THE CASE AGAINST EVOLUTION cell, both in its chemical composition and in its morphologi- cal structure, is an organism of extraordinary complexity. The protoplasm that it incloses is a mixture of very diverse substances. But if there be set aside on the one hand those substances which are in the process of assimilation and on the other those which are the by-products of nutrition, and which are in the process of elimination, there remain the protein or albuminous substances, and these must be con- sidered, if not the essential factor of life, at least the theater of its manifestations. . . . Chemistry, however, is totally ignorant, or nearly so, of the constitution of living albumen, for chemical methods of investigation at the very outset kill the living cell. The slightest rise in temperature, contact with the solvent, the very powerful effect of even the mildest reactions cause the transformation that needs to be pre- vented, and the chemist has nothing left but dead albumen." (Smithson. Inst. Rpt. for 1916, pp. 208, 209.) Chemical analysis associated with physical analysis by means of the polariscope, spectroscope, x-rays, ultramicro- scope, etc. is extremely useful in determining the structure of inorganic units like the atom and the molecule. Both, too, throw valuable light on the problem of the structure of non-living multimolecules such as the crystal units of crystal- loids and the ultramicrons of colloids, but they furnish no clue to the submicroscopical morphology of the living cell. Such methods do not enable us to examine anything more than the "physical substrate" of life, and that, only after it has been radically altered; for it is not the same after life has flown. At all events, the integrating principle, the forma- tive determinant, which binds the components of living pro- toplasm into a unitary system, which makes of them a single totality instead of a mere sum or fortuitous aggregate of disparate and uncoordinated factors, and which gives to them a determinate and persistent specificity that can hold its own amid a perpetual fluxion of matter and continual flow of energy, this is forever inaccessible to the chemist, and con- THE ORIGIN OF LIFE 146 stitutes a phenomenon of which the inorganic world affords no parallel: With these facts in mind, we can hardly fail to be amused whenever certain simple chemical reactions obtained in vitro are hailed as ''clue to the origin of life." When it was found, for instance, that, under certain conditions, an aldehyde (probably formaldehyde) is formed in a colloidal solution of chlorophyll in water, if exposed to sunlight, the discovery gave rise to Bach's formaldehyde-hypothesis; for Alexis Bach saw in this reaction "a first step in the origin of life." As for- maldehyde readily undergoes aldol condensation into a syrupy fluid called formose, when a dilute aqueous solution of for- maldehyde is saturated with calcium hydroxide and allowed to stand for several days, there was no difficulty in conceiving the transition from formaldehyde to the carbohydrates; for formose is a mixture containing several hexose sugars, and Fischer has succeeded in isolating therefrom acrose, a simple sugar having the same formula as glucose, namely: CsHioOs. Glyceraldehyde undergoes a similar condensation. In view of these facts, carbohydrate-production in green plants was interpreted as a photosynthesis of these substances from water and carbon dioxide, with chlorophyll acting a sensitizer to absorb the radiant energy necessary for the reaction. The first step in the process was thought to be a reduction of carbonic acid to formic acid and then to formaldehyde, the latter being at once condensed into glucose, which in turn was supposed to be dehydrated and polymerized into starch. From the carbohydrates thus formed and the nitrates of the soil the plant could then synthesize proteins, while oxidation of the carbohydrates into fatty acids would lead to the forma- tion of fats. Hence Bach regarded the formation of formal- dehyde in the presence of water, carbon dioxide, chlorophyll, and sunlight as the "first step in the production of life." Bateson, however, does not find the suggestion a very helpful one, and evaluates it at its true worth in the following contemptuous aside: "We should be greatly helped," he says, 146 THE CASE AGAINST EVOLUTION *'by some indication as to whether the origin of life has been single or multiple. Modern opinion is, perhaps, inclined to the multiple theory, but we have no real evidence. Indeed, the problem still stands outside the range of scientific investigation, and when we hear the spontaneous formation of formaldehyde mentioned as a possible first step in the origin of life, we think of Harry Lauder in the character of a Glasgow schoolboy pulling out his treasures from his pocket — "That's a wassher — for makkin' motor cars.'' ('Tresi- dential Address," cf. Smithson. Inst. Rpt. for 1915, p. 375.) Bach, moreover, takes it for granted that the formation of formaldehyde is really the first step in the synthesis per- formed by the green plant, and he claims that formaldehyde is formed when carbon dioxide is passed through a solution of a salt of uranium in the presence of sunlight. Fenton makes a similar claim in the case of magnesium, asserting that traces of formaldehyde are discernible when metallic magnesium is immersed in water saturated with carbon di- oxide. But at present it begins to look as though the spon- taneous formation and condensation of formaldehyde had nothing to do with the process that actually occurs in green plants. Certain chemists, while admitting that an aldehyde is formed when chlorophyll, water, and air are brought to- gether in the presence of sunlight, deny that the aldehyde in question is formaldehyde, and they also draw attention to the fact that this aldehyde may be formed in an atmosphere entirely destitute of carbon dioxide. In fact, the researches conducted by Willstatter and Stoll, and later (in 1916) by Jorgensen and Kidd tend to discredit the common notion that carbohydrate-production in plants is the result of a direct union of water and carbon dioxide. Botany textbooks still continue to parrot the traditional view. We cannot any longer, however, be sure but that the term photosynthesis may be a misnomer. Carbohydrate- formation in plants seems to be more anal- ogous to carbohydrate- formation in animals than was for- THE ORIGIN OF LIFE 147 merly thought to be the case. In animals, as is well known, glycogen or animal starch is formed not by direct synthesis, but by deamination and reduction of proteins. In a similar way, it is thought that the production of carbohydrates in plants may be due to a breaking down of the phytyl ester in chlorophyll, the chromogen group functioning (under the action of light) alternately as a dissociating enzyme in the formation of sugars and a synthesizing enzyme in the recon- struction of chlorophyll. Phytol is an unsaturated alcohol obtained when chlorophyll is saponified by means of caustic alkalis. Its formula is C20H39OH, and chlorophyll consists of a chromogen group containing magnesium (MgN4C32H3oO) united to a diester of phytyl and methyl alcohols. Experimental results are at variance with the theory that chlorophyll acts as a sensitizer in bringing about a reduction of carbonic acid, after the analogy of eosin, which in the presence of light accelerates the decomposition of silver salts on photographic plates. Willstatter found that, when a col- loidal solution of the pure extract of chlorophyll in water is exposed to sunlight and an atmosphere consisting of carbon dioxide exclusively, no formaldehyde is formed, but the chlorophyll is changed into yellow phseophytin owing to the removal of the magnesium from the chromogen group by the action of the carbonic acid. Jorgensen, on the other hand, discovered that in an atmosphere of pure oxygen, formal- dehyde is formed, apparently by the splitting off and re- duction of the phytyl ester of chlorophyll. Soon, however, the formaldehyde is oxidized to formic acid, which replaces the chlorophyllic magnesium with hydrogen, thus causing the green chlorophyll to degenerate into yellow phseophytin and finally to lose its color altogether. The dissociation of the chromogen group may be due to the fact that the reaction takes place in vitro, and may not occur in the living plant. At all events, it would seem that plants, like animals, manu- facture carbohydrates by a destructive rather than a con- structive process, and that water and carbon dioxide serve 148 THE CASE AGAINST EVOLUTION rather as materials for the regeneration of chlorophyll than as materials out of which sugars are directly synthesized. A new theory has been proposed by Dr. Oskar Baudisch, who seems to have sensed the irrelevance of the formaldehyde hypothesis, and to have sought another solution in connection with the chromogen group of chlorophyll. He finds a more promising starting-point in formaldoxime, which, he claims, readily unites with such metals as magnesium and iron and with formaldehyde, in the presence of light containing ultra- violet rays, to form organic compounds analogous to the chromogen complexes in chlorophyll and haemoglobin. Oximes are compounds formed by the condensation of one molecule of an aldehyde with one molecule of hydroxylamine (NH2OH) and the elimination of a molecule of water. Hence Dr. Baudisch imagines that, given formaldoxime (HaCiN'GH), magnesium, and ultra-violet rays, we might expect a spon- taneous formation of chlorophyll leading eventually to the production of organic life. "It is his theory that life may have been caused through the direct action of sunlight upon water, air, and carbon dioxide in the ancient geologic past when, he believes, sunlight was more intense and contained more ultra-violet light and the air contained more water vapor and carbon dioxide than at the present time." {Sci- ence, April 6, 1923, Supplement XII.) This is the old Spencerian evasion, the fatuous appeal to "conditions unlike those we know," the unverified and un- verifiable assumption that an unknown past must have been more favorable to spontaneous generation than the known present. In archseozoic times, the temperature was higher, the partial pressure of atmospheric carbon dioxide greater, the percentage of ultra-violet rays in sunlight larger. Such contentions are interesting, if true, but, for all that, they may, "like the flowers that bloom in the spring," have noth- ing to do with the case. Nature does not, and the laboratory cannot, reproduce the conditions which are said to have brought about the spontaneous generation of formaldoxime and its pro- THE ORIGIN OF LIFE 149 gressive transmutation into phycocyanin, chlorophyll and the blue-green algae. What value, then, have these conjectures? If it be the function of natural science to discount actualities in favor of possibilities, to draw arguments from ignorance, and to accept the absence of disproof as a substitute for demonstration, then the expedient of invoking the unknown in support of a speculation is scientifically legitimate. But, if the methods of science are observation and induction, if it proceeds according to the principle of the uniformity of nature, and does not utterly belie its claim of resting upon factual realities rather than the figments of fancy, then all this hypothecation, which is so flagrantly at variance with the actual data of experience and the unmistakable trend of inductive reasoning, is not science at all, but sheer credulity and superstition. When we ask by what right men of science presume to lift the veil of mystery from a remote past, which no one has observed, we are told that the justification of this pro- cedure is the principle of the uniformity of nature or the invariability of natural laws. Nature's laws are the same yesterday, to-day, and forever. Hence the scientist, who wishes to penetrate into the unknown past, has only to "pro- long the methods of nature from the present into the past." (Tyndall.) If we reject the soundness of this principle, we automatically cut ourselves off from all certainty regarding that part of the world's history which antecedes human ob- servation. Either nature's laws change, or they do not. If they never change, then Spontaneous Generation is quite as much excluded from the past as it is from the present. If, however, as Hamann and Fechner explicitly maintain, nature's laws do change, then, obviously, no knowledge whatever is possible respecting the past, since it is solely upon the as- sumption of the immutable constancy of such laws that we can venture to reconstruct prehistory. The puerile notion that the synthesis of organic substances in the laboratory furnishes a clue to the origin of organic 150 THE CASE AGAINST EVOLUTION life on earth is due to a confusion of organic, with living and organized, substances. It is only in the production of organic substances that the chemist can vie with the plant or animal. These are lifeless and unorganized carbon com- pounds, which are termed organic because they are elabo- rated by living organisms as a metaplastic by-product of their metabolism. Such substances, however, are not to be confounded with animate matter, e.g. a living cell and its organelles, or even with organized matter, e.g. dead proto- plasm. These the chemist cannot duplicate; for vitality and organization, as we have seen, are things that elude both his analysis and his synthesis. Even with respect to the pro- duction of organic substances, the parallelism between the living cell and the chemical laboratory is far from being a perfect one. Speaking of the metaplastic or organic products of cells, Benjamin Moore says: "Most of these are so com- plex that they have not yet been synthesized by the organic chemist; nay, even of those that have been synthesized, it may be remarked that all proof is wanting that the syntheses have been carried out in identically the same fashion and by the employment of the same forms of energy in the case of the cell as in the chemist's laboratory. The conditions in the cell are widely different, and at the temperature of the cell and with such chemical materials as are at hand in the cell no such organic syntheses have been artificially carried out by the forms of energy extraneous to living tissue." ("Re- cent Advances in Physiology and Bio-Chemistry," p. 10.) Be that as it may, however, the prospect of a laboratory syn- thesis of an organic substance like chlorophyll affords no ground whatever for expecting a chemical synthesis of living matter. The chlorophyllic tail is inadequate to the task of wagging the dog of organic life. In this connection, Yves Delage's sarcastic comment on Schaaffhausen's theory is worthy of recall. The latter had suggested (in 1892) that life was initiated by a chemical reaction, in which water, air, and mineral salts united under the influence of light and heat THE ORIGIN OF LIFE 151 to produce a colorless Protococcus, which subsequently ac- quired chlorophyll and became a Protococcus viridis. "If the affair is so simple," writes Delage, "why does not the author produce a few specimens of this protococcus in his laboratory? We will gladly supply him with the necessary chlorophyll." ("La structure du protoplasma et les theories sur I'heredite," p. 402.) Another consideration, which never appears to trouble the visionaries who propound theories of this sort, is the fact that the inert elements and blind forces of inorganic nature are, if left to themselves, utterly impotent to duplicate even so much as the feats of the chemical laboratory, to say noth- ing at all of the more wonderful achievements possible only to living organisms. In the laboratory, the physicochemical forces of the mineral world are coordinated, regulated, and directed by the guiding intelligence of the chemist. In that heterogeneous conglomerate, which we call brute matter, no such guiding principle exists, and the only possible automatic results are those which the fortuitous concurrence of blind factors avails to produce. Chance of this kind may vie with art in the production of relatively simple combinations or systems, but where the conditions are as complex as those, which the synthesis of chlorophyll presupposes, chance is impotent and regulation absolutely imperative. How much more is this true, when there is question of the production of an effect so complicatedly telic as the living organism I "I venture to think," says Sir William Tilden, in a letter to the London Times (Sept. 10, 1912), "that no chemist will be prepared to suggest a process^ by which, from the inter- action of such materials (viz., inorganic substances), anything approaching a substance of the nature of a proteid could be formed or, if by a complex series of changes a compound of this kind were conceivably produced, that it would present the characters of living protoplasm." In the concluding sen- tence of his letter, the great chemist seems to deprecate even the discussion of a chemical synthesis of living matter, whether 152 THE CASE AGAINST EVOLUTION spontaneous or artificial. "Far be it from any man of science," he says, "to affirm that any given set of phenomena is not a fit subject of inquiry and that there is any limit to what may be revealed in answer to systematic and well-directed investiga- tion. In the present instance, however, it appears to me that this is not a field for the chemist nor one in which chem- istry is likely to afford any assistance whatever." In any case, the idea that a chaos of unassorted elements and un- directed forces could succeed where the skill of the chemist fails is preposterous. No known or conceivable process, or group of processes, at work in inorganic nature, is equal to the task. Chance is an explanation only for minds insensible to the beauty and order of organic life. Darwin inoculated biological science with this Epicurean metaphysics, when, in his "Origin of Species," he ascribed discriminating and selective powers of great delicacy and precision to the blind factors of a heterogeneous and variable environment. He compared natural selection to artificial se- lection, and in so doing, he was led astray by a false impli- cation of his own analogy — "I have called this principle," he says, "by which each slight variation, if useful, is pre- served, by the term natural selection, in order to mark its relation to man's power of selection." ("Origin of Species," 6th ed., c. Ill, p. 58.) Having likened the unintelligent and fortuitous selection and elimination exercised by the environ- ment to the intelligent and purposive selection and elimination practiced by animal breeders and horticulturists, he pressed the analogy to the unwarranted extent of attributing to a blind, lifeless, and impersonal aggregate of minerals, liquids, and gases superhuman powers of discretion. To preserve even the semblance of parity, he ought first to have expur- gated the process of artificial selection by getting rid of the element of human intelligence, which lurks therein, and viti- ates its parallelism with the unconscious and purposeless havoc wrought at random by the blind and uncoordinated agencies of the environment. If inorganic nature were a vast THE ORIGIN OF LIFE 153 and multifarious mold, a preformed sieve with holes of differ- ent sizes, a separator for sorting coins of various denomina- tions, Darwin's idea would be,, in some degree, defensible, but this would only transfer the problem of cosmic order and intelligence from the organism to the environment. As a matter of fact, the mechanism of the environment is far too simple in its structure and too general in its influence to account for the complexities and specificities of organisms, that is, for the morphology and specific differences of plants and animals. Hence the selective work of the environment is negligible in the positive sense, and consists, for the most part, in a tendency to eliminate the abnormal and the sub- normal. On the other hand, the environment as well as the organism is fundamentally teleological, and the environ- mental mechanism, though simple and general, is neverthe- less expressly preadapted for the maintenance of organic life. Henderson, the bio-chemist of Harvard, has shown conclu- sively, in his "Fitness of the Environment" (1913), that the environment itself has been expressly selected with this final- ity in view, and that the inorganic world, while not the active cause, is, nevertheless, the preordained complement of or- ganic life. Simple constructions may, indeed, be due to pure accident as well as deliberate art, inasmuch as they presuppose but few and easy conditions. Complex constructions, on the contrary, provided they be systematic and not chaotic, are not pro- ducible by accident, but only by art, because they require numerous and complicated conditions. Operating individu- ally, the unconscious factors of inorganic nature can produce simple and homogeneous constructions such as crystals. Op- erating in uncoordinated concurrence with one another, these blind and unrelated agencies produce complex chaotic for- mations such as mountains and islands, mere heterogeneous conglomerates, destitute of any determinate size, shape, or symmetry, constructions in which every single item and detail is the result of factors each of which is independent of the 154 THE CASE AGAINST EVOLUTION other. In short, the efficacy of the unconscious and unco- ordinated physicochemical factors of inorganic nature is lim- ited to fortuitous results, which serve no purpose, embody no intelligible law, convey no meaning nor idea, and afford no sesthetic satisfaction, being mere aggregates or sums rather than natural units and real totalities. But it does not extend to the production of complex systematic formations such as living or- ganisms or human artefacts. Left to itself, therefore, inor- ganic nature might conceivably duplicate the simplest arte- facts such as the chipped flints of the savage, and it might also construct a complex heterogeneous chaos of driftwood, mud, and sand like the Great Raft of the Red River, but it would be utterly impotent to construct a complicated telic system comparable to an animal, a clock, or even an organic compound, like chlorophyll. In this connection, it is curious to note how extremely myopic the scientific materialist can be, when there is ques- tion of recognizing a manifestation of Divine intelligence in the stupendous teleology of the living organism, and how in- credibly lynx-eyed he becomes, when there is question of de- tecting evidences of human intelligence in the eoliths alleged to have been the implements of a "Tertiary Man." In the latter case, he is never at a loss to determine the precise degree of chipping, at which an eolith ceases to be inter- pretable as the fortuitous product of unconscious processes, and points infallibly to the intelligent authorship of man, but he grows strangely obtuse to the psychic implications of teleology, when it comes to explaining the symmetry of a starfish or the beauty of a Bird of Paradise. In conclusion, it is clear that the hypothesis of a spon- taneous origin of organic life from inorganic matter has in its favor neither factual evidence nor aprioristic probability, but is, on the contrary, ruled out of court by the whole force of the scientific principle of induction. To recapitulate, there are no sub-cellular organisms, and all cellular organisms (which is the same as saying, all organisms), be they unicellular or THE ORIGIN OF LIFE 155 multicellular, originate exclusively by reproduction, that is, by generation from living parents of the same organic type or species. This is the law of genetic vital continuity, which, by the way, Aristotle had formulated long before Harvey, when he said: "It appears that all living beings come from a germ, and the germ from parents." ("De Generatione Animalium," lib. I, cap. 17.) All reproduction, however, is reducible to a process of cell-division. That such is the case with unicellular or- ganisms is evident from the very definition of a cell. That it is also true of multicellular organisms can be shown by a review of the various forms of reproduction occurring among plants and animals. § 4. Reproduction and Rejuvenation Reproduction, the sole means by which the torch of life is relayed from generation to generation, the exclusive process by which living individuals arise and races are perpetuated, consists in the separation of a germ from the parent organ- ism as a physical basis for the development of a new organ- ism. The germ thus separated may be many-celled or one- celled, as we shall see presently, but the separated cells, be they one or many, have their common and exclusive source in the process of mitotic cell-division. In a few cases, this di- visional power or energy of the cell seems to be perennial by virtue of an inherent inexhaustibility. In most cases, however, it is perennial by virtue of a restorative process involving nuclear reorganization. In the former cases, which are exceptional, the cellular stream of life appears to flow onward forever with steady current, but as a general rule it ebbs and flows in cycles, which involve a periodic rise and fall of divisional energy. The phenomena of the life-cycle are characteristic of most, perhaps all, organisms. The com- plete life-cycle consists of three phases or periods, namely: an 'adolescent period of high vitality, a mature period of balanced metabolism, and a senescent period of decline. Each life-cycle begins with the germination of the new organism 156 THE CASE AGAINST EVOLUTION and terminates with its death, and it is reproduction which constitutes the connecting link between one life-cycle and another. Reproduction, as previously intimated, is mainly of two kinds, namely: somatogenic reproduction, which is less gen- eral and confined to the metists, and cytogenic reproduction, which is common to metists and protists, and which is the ordinary method by which new organisms originate. Repro- duction is termed somatogenic, when the germ separated from the body of the parent consists of a whole mass of somatic or tissue cells not expressly set aside and specialized for reproductive purposes. Reproduction is termed cytogenic, when the germ separated from the parent or parents consists of a single cell (e.g. a spore, gamete, or zygote) dedicated especially to reproductive purposes. Cytogenic reproduction may be either nonsexual (agamic) or sexual, according as the cell which constitutes the germ is an agamete or a gamete. An agamete is a germ cell not specialized for union with another complementary cell, or, in other words, it is a reproductive cell incapable of syngamy, e.g. a spore. A gamete, on the other hand, is a reproductive cell (germ cell) specialized for the production of a zygote (a synthetic or diploid germ cell) by union with a comple- mentary cell, e.g. an egg, or a sperm. Nonsexual cytogenic reproduction is of three kinds, ac- cording to the nature of the agamete. When a unicellular organism gives rise to two new individuals by simple cell- division, we have fissiparation or binary fission. When a small cell or bud is formed and separated by division from a larger parent cell, we have budding (gemmation) or un- equal fission. When the nucleus of the parent cell divides many times to form a number of daughter-nuclei, which then partition the cytoplasm of the parent cell among them- selves so as to form a large number of reproductive cells called spores, we have what is known as sporulation or multiple fission. The first and second kind of nonsexual THE ORIGIN OF LIFE 157 reproduction are confined to the protists, but the third kind (sporulation) also occurs among the metists. Seyial cytogenic reproduction is based upon gametes or mating germ cells. Since complementary gametes are spe- cialized for union with each other to form a single synthetic cell, the zygote, the number of their nuclear threads or chro- mosomes is reduced to one half (the haploid number) at the time of maturation, so that the somatic or tissue cells of the parent organism have double the number (the diploid num- her) of chromosomes present in the reduced or mature gametes. Hence, when the gametes unite to form a zygote, summation is prevented and the diploid number of chromosomes char- acteristic of the given species of plant or animal is simply restored by the process of syngamy or union. The process by which the number of chromosomes is reduced in gametes is called meiosis, and, among the metists, it is distinct from syngamy, which, in their case, is a separate process called fertilization. Among the protists, we have, besides fertiliza- tion, another type of syngamy called conjugation, which combines meiosis with fertilization. In sexual reproduction, we have three kinds of gametes, namely: isogametes, anisogametes, and heterogametes. In the type of sexual reproduction known as isogamy, the com- plementary gametes are exactly alike both in size and shape. There is no division of labor between them. Each of the fusing gametes is equally fitted for the double function which they must perform, namely, the kinetic function, which en- ables them to reach each other and unite by means of move- ment, and the trophic function which consists in laying up a store of food for the sustenance of the developing embryo. In anisogamy, the complementary gametes are alike in shape, but unlike in size, and here we have the beginning of that division of labor, upon which the difference of gender or sex is based. The larger or female gamete is called a macro- gamete. It is specialized for the trophic rather than the kinetic function, being rendered more inert by having a large 158 THE CASE AGAINST EVOLUTION amount of yolk or nutrient material stored up within it. The smaller or male gamete is called a microgamete. It is specialized for the kinetic function, since it contains less yolk and is the more agile of the two. In anisogamy, however, the division of labor is not complete, because both functions are still retained by either gamete, albeit in differing measure. In the heterogamy, the differentiation between the male and female gametes is complete, and they differ from each other in structure as well as size. The larger or female gamete has no motor apparatus and retains only the trophic func- tion. The kinetic function is sacrificed to the task of storing up a food supply for the embryo. Such a gamete is called a hypergamete or egg. The smaller or male gamete is known, in this case, as a hypogamete or sperm. It has a motor apparatus, but no stored-up nutrients, and has even sloughed off most of its cytoplasm, in its exclusive specialization for the motor function. In heterogamy, accordingly, the division of labor is complete. We may distinguish two principal kinds of sexual repro- duction, namely: unisexual reproduction and bisexual repro- duction. When a single gamete such as an unfertilized egg gives rise (with, or without, chromosomal reduction) to a new organism, we have unisexual reproduction or parthenogenesis. Parthenogenesis from a reduced egg gives rise to an organism having only the haploid number of chromosomes, as is the case with the drone or male bee, but unreduced eggs give rise to organisms having the diploid number of chromosomes. Parthenogenesis, as we shall see presently, can, in some cases, be induced by artificial means. When reproduction takes place from a zygote or diploid germ cell formed by the union of two gametes, we have what is known as bisexual reproduction or syngamy. It is, perhaps, permissible to distinguish a third or intermediate kind of sexual reproduction, for which we might coin the term autosexual. What we refer to as autosexual reproduction is usually known as autogamy, and occurs when a diploid nucleus is formed in a germ THE ORIGIN OF LIFE 159 cell by the union (or, we might say, reunion) of two daughter-nuclei derived from the same mother-nucleus. Au- togamy occurs not only among the protists {e.g. Amoeba albida), but also among the metists, as is the case with the brine shrimp, Artemia salina, in which the diploid number of chromosomes is restored after reduction by a reunion of the nucleus of the second polar body with the reduced nu- cleus of the egg. Autogamy is somewhat akin to kleistogamy, which occurs among hermaphroditic metists of both the plant and animal kingdoms. The violet is a well-known example. In kleistogamy or self-fertilization, the zygote is formed by the union of two gametes derived from the same parent organism. Strictly speaking, however, kleistogamy is not autogamy, but syngamy, and must, therefore, be classed as bisexual reproduction. It is, of course, necessarily confined to hermaphrodites. Loeb's experiments in artificial parthenogenesis have been sensationally misinterpreted by some as an artificial produc- tion of life. What Jacques Loeb really did was to initiate devel- opment in an unfertilized egg by the use of chemical and phys- ical excitants. The writer has repeated these experiments with the unfertilized eggs of the common sea urchin, Arbacia punc- tulata, using very dilute butyric acid and hypertonic sea water as stimulants. Cleavage had started within an hour and a half after the completion of the aforesaid treatment, and the eggs were in the gastrula stage by the following morn- ing (9 hours later). In three days, good specimens of the larval stage known as the pluteus could be found swimming in the normal sea water to which the eggs had been trans- ferred from the hypertonic solution. Since mature sea urchin eggs undergo reduction before insemination takes place, the larval sea urchins arising from these artificially activated eggs had the reduced or haploid number of chromosomes in- stead of the diploid number possessed by normal larvae arising from eggs activated by the sperm. For, in fertilization, the sperm not only activates the egg, but is also the means of secur- 160 THE CASE AGAINST EVOLUTION ing biparental inheritance, by contributing its quota of chromo- somes to the zygotic complex. Hence, it is only in the former function, i.e. of initiating cleavage in the egg, that a chemical excitant can replace the sperm. In any case, it is evident that these experiments do not constitute an exception to the law of genetic cellular continuity. The artificially activated egg comes from the ovaries of a living female sea urchin, and in this there is small consolation for the exponent of abiogenesis. The terse comment of an old Irish Jesuit sizes up the situation very aptly: "The Blue Flame Factory," he said, "has an- nounced another discovery of the secret of life. A scientist made an egg and hatched an egg. The only unfortunate thing was that the egg he hatched was not the egg he made." How an experiment of this sort could be interpreted as an artificial production of life is a mystery. The only plausible explanation is that given by Professor Wilson, who traces it to the popular superstition that the egg is a lifeless substrate, which is animated by the sperm. The idea owes its origin to the spermists of the 17th century, who defended this doctrine against the older school of preformationists known as ovists. It is now, however, an embryological commonplace that egg and sperm are both equally cellular, equally protoplasmic, and equally vital. The phenomena of the life-cycle in organisms find their ex- planation in what, perhaps, is inherent in all living matter, namely, a tendency to involution and senescence. This ten- dency, in the absence of a remedial process of rejuvenation, leads inevitably to death. Living matter seems to "run down" like a clock, and to stand in similar need of a periodic "rewind- ing." This reinvigoration of protoplasm is accomplished by means of several different types of nuclear reorganization. Since no nuclear reorganization occurs in somatogenic re- production, there seem to be limits to this type of propaga- tion. Plants, like the potato and the apple, cannot be propa- gated indefinitely by means of tubers, shoots, stems, etc. The stock plays out in time, and, ever and anon, recourse must THE ORIGIN OF LIFE 161 be had to seedlings. Hence a process of nuclear reorgani- zation seems, in most cases, at least, to be essential for the restoration of vitality and the continuance of life. Whether this need of periodic renewal is absolutely universal, we can- not sa5^ The banana has been propagated for over a century by the somatogenic method, and there are a few other in- stances in which there appears to be no limit to this type of reproduction. Nevertheless, the tendency to decline is so common among living beings that the rare exceptions serve only to confirm (if they do not follow) the general rule. In cytogenic reproduction three kinds of rejuvenation by means of nuclear reorganization are known: (1) amphimixis or syngamy; (2) automixis or autogamy; (3) endomixis. In amphimixis or syngamy, two gametic (haploid) nuclei of dif- ferent parental lineage are commingled to form the diploid nucleus of the zygote, which is consequently of biparental ori- gin. In automixis or autogamy, two reduced or haploid nuclei of the same parental lineage unite to form a diploid nucleus, the uniting nuclei being daughter-nuclei derived from a com- mon parent nucleus. In endomixis, the nucleus of the ex- hausted cell disintegrates and fuses with the cytoplasm, out of which it is reformed or reconstructed as the germinal nu- cleus of a rejuvenated cellular series. Endomixis occurs as a periodic phenomenon among the protists, and it appears to be homologous with parthenogenesis among metists. In cer- tain ciliates, like the Paramoecium, endomixis and syngamy are facultative methods of rejuvenation. This has been proved most conclusively by Professor Calkins' work on Uroleptus mohilis, an organism in which both endomixis and conjugation are amenable to experimental control. Nonsexual reproduc- tion in this protozoan (by binary fission) is attended with a gradual weakening of metabolic activity, which increases with each successive generation. The initial rate of di- vision and metabolic energy can, however, be restored either by conjugation (of two individuals), or by endomixis, which takes place (in a single individual) during encyst- m THE CASE AGAINST EVOLUTION ment. The race, however, inevitably dies out, if both encystment and conjugation are prevented. Even in such protists as do not exhibit the phenomenon of nuclear reorganization through sexual reproduction, Kofoid points to the phenomenon of alternating periods of rest and rapid cell-division as evidence that some process of periodically- recurrent nuclear organization must exist in the organisms, which do not conjugate. This process of nuclear reorgani- zation manifested by periodic spurts of renewed divisional energy is, according to Kofoid, a more primitive mode of rejuvenation than endomixis. "The phenomenon of endo- mixis," he says, "appears to be somewhat more like that of parthenogenesis than a more primitive form of nuclear re- organization." {Science, April 6, 1923, p. 403.) At all events, it seems safe to conclude that the tendency to senescence is pretty general among living organisms, and that this tendency, unless counteracted by a periodic reorganization of the nuclear genes, results inevitably in the deterioration and final ex- tinction of the race. In this inexhaustible power of self-renewal inherent in all forms of organic life, the mechanist and the upholder of abiogenesis encounter an insuperable difficulty. In inorganic nature, where the perpetual-motion device is a chimera, and the law of entropy reigns in unchallenged supremacy, noth- ing analogous to it can be found. The activity of all non- living units of nature, from the hydrogen atom to the protein multimolecule, is rigidly determined by the principle of the degradation of energy. The inorganic unit cannot operate otherwise than by externalizing and dissipating irreparably its own energy-content. Nor is its reconstruction and replenish- ment with energy ever again possible except through the wasteful expenditure of energy borrowed from some more richly endowed inorganic unit. In order to pay Paul a little, Peter must be robbed of much. Wheresoever atoms are built up into complex endothermic molecules, the constructive THE ORIGIN OF LIFE 163 process is rigidly dependent upon the administration thereto of external energy, which in the process of absorption must of necessity fall from a higher level of intensity. And when the energy thus absorbed by the complex molecule is again set free by combustion, it is degraded to a still lower po- tential, from which, without external intervention, it can never rise again to its former plane of intensity. The phenomena of radioactivity tell the same tale. All the heavier atoms, at least, are constantly disintegrating with a concomitant discharge of energy. There is no compensating process, how- ever, enabling such an atom to re-integrate and recharge itself at stated intervals ; and, once it has broken down into its com- ponent protons and electrons, ''not all the king's horses nor all the king's men can ever put Humpty-Dumpty together again." In a word, none of the inorganic units of the mineral world exhibits that wonderful power of autonomous recupera- tion which a unicellular ciliate manifests when it rejuvenates itself by means of endomixis. The inorganic world knows of no constructive process comparable to this. It is only in living beings that we find what James Ward describes as the "tendency to disturb existing equilibria, to reverse the dissi- pative processes which prevail throughout the inanimate world, to store and build up where they are ever scattering and pulling down, the tendency to conserve individual ex- istence against antagonistic forces, to grow and to progress, not inertly taking the easier way but seemingly striving for the best, retaining every vantage secured, and working for new ones." ("On the Conservation of Energy," I, p. 285.) Summing up, then, we have seen that the reproductive process, whereby the metists or multicellular organism origi- nate, resolves itself ultimately into a process of cell-division. The same is true of the protists or unicellular organisms. For all cells, whether they be protists, germ cells, or somatic cells, originate in but one way, and that is, from a preexistent liv- ing cell by means of cell-division. Neither experimentation 164 THE CASE AGAINST EVOLUTION nor observation has succeeded in revealing so much as a single exception to the universal law of genetic cellular continuity, and the hypothesis of spontogenesis is outlawed, in consequence, by the logic of scientific induction. Even the hope that future research may bring about an amelioration of its present status is entirely unwarranted in view of the manifest dynamic su- periority of the living organism as compared with any of the inert units of the inorganic world. ''Whatever position we take on this question," says Edmund B. Wilson, in the con- clusion of his work on the Cell, "the same difficulty is en- countered; namely, the origin of that coordinated fitness, that power of active adjustment between internal and external relations, which, as so many eminent biological thinkers have insisted, overshadows every manifestation of life. The nature and origin of this power is the fundamental problem of biol- ogy. When, after removing the lens of the eye in the larval salamander, we see it restored in perfect and typical form by regeneration from the posterior layer of the iris, we be- hold an adaptive response to changed conditions of which the organism can have no antecedent experience either onto- genetic or phylogenetic, and one of so marvelous a char- acter that we are made to realize, as by a flash how far we still are from a solution of this problem." Then, after dis- cussing the attempt of evolutionists to bridge the enormous gap that separates living, from lifeless nature, he continues: "But when all these admissions are made, and when the con- serving action (sic) of natural selection is in the fullest de- gree recognized, we cannot close our eyes to two facts: first, that we are utterly ignorant of the manner in which the idioplasm of the germ cell can so respond to the influence of the environment as to call forth an adaptive variation; and second, that the study of the cell has on the whole seemed to widen rather than to narrow the enormous gap that sepa- rates even the lowest forms of life from the inorganic world." ("The Cell," 2nd edit., pp. 433, 434.) THE ORIGIN OF LIFE 165 § 5. A "New" Theory of Abiogenesis Since true science is out of sympathy with baseless conjec- tures and gratuitous assumptions, one would scarcely expect to find scientists opposing the inductive trend of the known facts by preferring mere possibilities (if they are even such) to solid actualities. As a matter of fact, however, there are not a few who obstinately refuse to abandon preconceptions for which they can find no factual justification. The bio-chemist, Benjamin Moore, while conceding the bankruptcy of the old theory of spontaneous generation, which looked for a de novo origin of living cells in sterilized cultures, has, nevertheless, the hardihood to propose what he is pleased to term a new one. Impressed by the credulity of Charlton Bastian and the auto- cratic tone of Schafer, he sets out to defend as plausible the hypothesis that the origination of life from inert matter may be a contemporaneous, perhaps, daily, phenomenon, going on continually, but invisible to us, because its initial stages take place in the submicroscopic world. By the time life has emerged into the visible world, it has already reached the stage at which the law of genetic continuity prevails, but at stages of organization, which lie below the limit of the micro- scope, it is not impossible, he thinks, that abiogenesis may oc- cur. To plausibleize this conjecture, he notes that the cell is a natural unit composed of molecules as a molecule is a natural unit composed of atoms. He further notes, that, in addition to the cell, there is in nature another unit higher than the mono- molecule, namely, the multimolecule occurring in both crystal- loids and colloids. The monomolecule consists of atoms held together by atomic valence, whereas the multimolecule con- sists of molecules whose atomic valence is completely sat- urated, and which are, consequently, held together by what is now known as molecular or residual valence. Moore cites the crystal units of sodium bromide and sodium iodide as in- stances of multimolecules. The crystal unit of ordinary salt, sodium chloride, is an ordinary monomolecule, with the for- 166 THE CASE AGAINST EVOLUTION mula NaCl. In the case of the former salts the crystal units consist of multimolecules of the formula NaB -(1120)2 and Nal -(1120)2, the water of crystallization not being mechani- cally confined in the crystals, but combined with the respec- tive salt in the exact ratio of two molecules of water to one of the salt. Judged by all chemical tests, such as heat of formation, the law of combination in fixed ratios, the mani- festation of selective affinity, etc., the multimolecule is quite as much entitled to be considered a natural unit as is the monomolecule. But it is not in the crystalloidal multimolecule, but in the larger and more complex multimolecule of colloids (viscid sub- stances like gum arable, gelatine, agar-agar, white of egg, etc.), that Moore professes to see a sort of intermediate be- tween the cell and inorganic units. Such colloids form with a dispersing medium (like water) an emulsion, in which the dispersed particles, known as ultramicrons or "solution ag- gregates," are larger than monomolecules. It is among these multimolecules of colloids that Moore would have us search for a transitional link connecting the cell with the inorganic world. Borrowing Herbert Spencer's dogma of the compli- cation of homogeneity into heterogeneity, he asserts that such colloidal multimolecules would tend to become more and more complex, and consequently more and more instable, so that their instability would gradually approach the chronic insta- bility or constant state of metabolic fluxion manifest in living organisms. The end-result would be a living unit more simply organized than the cell, and evolution seizing upon this sub- microscopic unit would, in due time, transform it into cellular life of every variety and kind. Ce n'est que le premier pas qui coute! It should be noted that this so-called law is a mere vague formula like the *'law" of natural selection and the "law'^ of evolution. The facts which it is alleged to express are not cited, and its terms are far from being quantitative. It is certainly not a law in the sense of Arrhenius, who says: THE ORIGIN OF LIFE 167 ^'Quantitative formulation, that is, the establishing of a con- nection,, expressed by a formula, between different quanti- tatively measurable magnitudes, is the peculiar feature of a law." ("Theories of Chemistry," Price's translation, p. 3.) Now, chemistry, as an exact science, has no lack of laws of this kind, but no branch of chemistry, whether physical, organic, or inorganic, knows of any law of complexity, that can be stated in either quantitative, or descriptive, terms. We will, however, let Moore speak for himself: "It may then be summed up as a general law universal in its application to all matter, ... a law which might be called the Law of Complexity, that matter so far as its en- ergy environment will permit tends to assume more and more complex forms in labile equilibrium. Atoms, molecules, col- loids, and living organisms, arise as a result of the operations of this law, and in the higher regions of complexity it induces organic evolution and all the many thousands of living forms. . . . "In this manner we can conceive that the hiatus between non-living and living things can be bridged over, and there awakens in our minds the conception of a kind of spontaneous production of life of a different order from the old. The territory of this spontaneous generation of life lies not at the level of bacteria, or animalculae, springing forth into life from dead organic matter, but at a level of life lying deeper than anything the microscope can reveal, and possessing a lower unit than the living cell, as we form our concept of it from the tissues of higher animals and plants. "In the future, the stage at which colloids begin to be able to deal with external energy forms, such as light, and build up in chemical complexity, will yield a new unit of life opening a vista of possibilities as magnificent as that which the establishment of the cell as a unit gave, with the development of the microscope, about a century ago." ("Ori- gin and Nature of Life," pp. 188-190.) Having heard out a rhapsody of this sort, one may be 168 THE CASE AGAINST EVOLUTION pardoned a little impatience at such a travesty on science. Again we have the appeal from realities to fancies, from the seen to unseen. Moore sees no reason to doubt and is there- fore quite sure that an unverified occurrence is taking place "at a level of life lying deeper than anything the microscope can reveal." The unknown is a veritable paradise for irre- sponsible speculation and phantasy. It is well, however, to keep one's feet on the terra firma of ascertained facts and to make one's ignorance a motive for caution rather than an incentive to reckless dogmatizing. To begin with, it is not to a single dispersed particle or ultramicron that protoplasm has been likened, but to an emul- sion, comprising both the dispersed particles and the dispersing medium, or, in other words, to the colloidal system as a whole. Moreover, even there the analogy is far from being perfect, and is confined exclusively, as Wilson has pointed out, to a rough similarity of structure and appearance. The colloidal system is obviously a mere aggregate and not a natural unit like the cell, and its dispersed particles (ultramicrons) do not mul- tiply and perpetuate themselves by growth and division as do the living components or formed bodies of the cell. As for the single ultramicron or multimolecule of a colloidal solu- tion, it may, indeed, be a natural unit, but it only resembles the cell in the sense that, like the latter, it is a complex of constituent molecules. Here, however, all resemblance ceases; for the ultramicron does not display the typically vital power of self-perpetuation by growth and division, which, as we have seen, is characteristic not only of the cell as a whole, but of its single components or organelles. Certainly, the dis- tinctive phenomena of colloidal systems cannot be interpreted as processes of multiplication. There is nothing suggestive of this vital phenomenon in the reversal of phase, which is caused by the addition of electrolytes to oil emulsions, or in gelation, which is caused by a change of temperature in certain hydro- philic colloids. Thus the addition of the salt of a bivalent cation (e.g. CaCl? or BaClg) to an oil-in-water emulsion (if THE ORIGIN OF LIFE 169 soap is used as the emulsifier) will cause the external or continuous phase (water) to become the internal or discon- tinuous phase. Vice versa, a water-in-oil emulsion can be reversed into an oil-in-water emulsion, under the same con- ditions, by the addition of the salt of a monovalent cation {e.g. NaOH). Solutions of hydrophilic colloids, like gelatine or agar-agar, can be made to "set" from the semifluid state of a hydrosol into the semisolid state of a hydrogel, by low- ering the temperature, after which the opposite effect can be brought about by again raising the temperature. In white of egg, however, once gelation has taken place, through the agency of heat, it is impossible to reconvert the "gel" into a "sol" (solution). In such phenomena, it is, perhaps, possible to see a certain parallelism with some processes taking place in the cell, e.g. the osmotic processes of absorption and excre- tion, but to construe them as evidence of propagation by growth and division would be preposterous. Nor is the subterfuge of relegating the question to the obscurity of the submicroscopic world of any avail; for, as a matter of fact, submicroscopic organisms actually do exist, and manage, precisely by virtue of this uniquely vital power of multiplication or reproductivity, to give indirect testimony of their invisible existence. The microorganisms, for exam- ple, which cause the disease known as Measles are so minute that they pass through the pores of a porcelain filter, and are invisible to the highest powers of the microscope. Never- theless, they can be bred in the test tube cultures of the bacteriologist, where they propagate themselves for genera- tions without losing the definite specificity, which make them capable of producing distinctive pathological effects in the or- ganisms of higher animals, including man. Each of these invisible disease germs communicates but one disease, with symptoms that are perfectly characteristic and definite. Moreover, they are specific in their choice of a host, and will not infect any and every organism promiscuously. Finally, they never arise de novo in a healthy host, but must 170 THE CASE AGAINST EVOLUTION always be transmitted from a diseased to a healthy indi- vidual. The microscopist is tantalized, to quote the words of Wilson, "with visions of disease germs which no eye has yet seen, so minute as to pass through a fine filter, yet be- yond a doubt self-perpetuating and of specific type." {Sci- ence, March 9, 1923, p. 283.) Submicroscopic dimensions, therefore, are no obstacle to the manifestation of such vital properties as reproduction, genetic continuity, and typical specificity; and we must conclude that, if any of the ultra- microns of colloids possessed them, their minute size would not debar them from manifesting the fact. As it is, they fail to show any vital quality, whereas the submicroscopic dis- ease germs give evidence of possessing all the characteristics of visible cells. In fine, the radical difference between inorganic units, like atoms, molecules, and multimolecules, and living units, like protozoans and metazoans, is so obvious that it is univer- sally admitted. Not all, however, are in accord when it comes to assigning the fundamental reason for the difference in question. Benjamin Moore postulates a unique physical en- ergy, peculiar to living organisms and responsible for all dis- tinctively vital manifestations. This unique form of energy, unlike all other forms, he calls "biotic energy," denying at the same time that it is a vital force. (Cf. op. cit, pp. 224- 226.) Moore seems to be desirous of dressing up vitalism in the verbal vesture of mechanism. He wants the game, with- out the name. But, if his ''biotic energy" is unlike all other forms of energy, it ought not to parade under the same name, but should frankly call itself a "vital force." Somewhat similar in nature is Osbom's suggestion that the peculiar properties of living protoplasm may be due to the presence of a unique chemical element called Bion. (Cf. "The Origin and Evolution of Life," 1917, p. 6.) Now, a chemical element unlike other chemical elements is not a chemical element at all. Osborn's Bion, like Moore's biotic energy, ought, by all means, to make up its mind definitely on Hamlet's question THE ORIGIN OF LIFE 171 of "to be, or not to be." The policy of "It is, and it is not," is- not likely to win the approval of either mechanists or vitalists. § 6. Hylomorphism versus Mechanism and Neo-vitalism Mechanism and Neo-vitalism represent two extreme solu- tions of this problem of accounting for the difference between living and lifeless matter. Strictly speaking, it is an abuse of language to refer to mechanism as a solution at all. Its first pretense at solving the problem is to deny that there is any problem. But facts are facts and cannot be disposed of in this summary fashion. Forced, therefore, to face the actual fact of the uniqueness of living matter, mechanists concede the inadequacy of their physicochemical analogies, but obstinately refuse to admit the legitimacy of any other kind of explanation. Confronted with realities, which simply must have some explanation, they prefer to leave them un- explained by their own theory than have them explained by any other. They recognize the difference between a living ani- mal and a dead animal (small credit to them for their per- spicacity!), but deny that there is anything present in the former which is not present in the latter. Neo-vitalism, on the other hand, is, at least, an attempt at solving the problem in the positive sense. It ascribes the unique activities of living organisms to the operation of a superphysical and superchemical energy or force resident in living matter. This unique dynamic principle is termed vital force. It is not an entitive nor a static principle, but belongs to the category of efficient or active causes, being variously de- scribed as an agent, energy, or force. To speak precisely, the term agent denotes an active being or substance; the term energy denotes the proximate ground in the agent of a spe- cific activity; while the term force denotes the activity or free, kinetic, or activated phase of a given energy. In practice, however, these terms are often used interchangeably. Thus Driesch, who, like all other Neo-vitalists, makes the vital prin- 172 THE CASE AGAINST EVOLUTION ciple a dynamic factor rather than an entitive principle, refers to the vital principle as a "non-material," "non-spatial" agent, though the term energy would be more precise. To this active or dynamic vital principle Driesch gives a name, which he borrowed from Aristotle, that is, entelechy. In so doing, however, he perverted, as he himself confesses, the true Aristotelian sense of the term in question: "The term," he says, ". . . is not here used in the proper Aristotelian sense." ("History and Theory of Vitalism," p. 203.) His admission is quite correct. At the critical point, Driesch, for all his praise of Aristotle, deserts the Stagirite and goes over to the camp of Plato, Descartes, and the Neo-vitalists ! Driesch's definition is as follows: "Entelechy is an agent sui generis, non-material and non-spatial, but acting 'into' space." {Op. cit., p. 204.) Aristotle's use of the term in this connection is quite different. He uses it, for example, in a static, rather than a dynamic, sense: "The term 'entelechy,' " he says, "is used in two senses; in one it answers to knowl- edge, in the other to the exercise of knowledge. Clearly in this case it is analogous to knowledge." ("Peri Psyches," Bk. II, c. 1.) Knowledge, however, is only a second or static entelechy. Hence, in order to narrow the sense still further Aristotle refers to the send as a first entelechy, by which he designates a purely entitive principle, that is, a constitu- ent of being or substance (cf. op. cit. ibidem). The first, or entitive, entelechy, therefore, is to be distinguished from all secondary entelechies, whether of the dynamic order corre- sponding to kinetic energy or force, or of the static order corre- sponding to potential energy. Neither is it an agent, because it is only a partial constituent of the total agent, that is, of the total active being or substance. Hence, generally speaking, that which acts (the agent) is not entelechy, but the total composite of entelechy and matter, first entelechy being consubstantial with matter and not a separate existent or being. In fine, according to Aristotelian philosophy, entelechy (that is, "first" or "prime" entelechy) is not an agent nor an energy THE ORIGIN OF LIFE 173 nor a force. In other words, it is totally removed from the category of efficient or active causes. The second difference between Driesch and Aristotle with respect to the use of the term entelechy lies in the fact that Driesch uses it as a synonym for the soul or vital principle, whereas, according to Aristotle, entelechy is common to the non-living units of in- organic nature as well as the living units (organisms) of the organic world. All vital principles or souls are entelechies, but not all entelechies are vital principles. All material beings or substances, whether living or lifeless, are reducible, in the last analysis, to two consubstantial principles or complementary constituents, namely, entelechy and mat- ter. Entelechy is the binding, type-determining principle, the source of unification and specification, which makes of a given natural unit (such as a molecule or a proto- zoan) a single and determinate whole. Matter is the de- terminable and potentially-multiplei element, the principle of divisibility and quantification, which can enter indifferently into the composition of this or that natural unit, and which owes its actual unity and specificity to the entelechy which here and now informs it. It is entelechy which makes a chemical element distinct from its isobare, a chemical com- pound distinct from its isomer, a paramoecium distinct from an amoeba, a maple distinct from an oak, and a bear distinct from a tiger. The molecular entelechy finds expression in what the or- ganic chemist and the stereochemist understand by valence, that is, the static aspect of valence considered as the struc- tural principle of a molecule. Hence it is entelechy which makes a molecule of urea [0:C:(NH2)2] an entirely dif- ferent substance from its isomer ammonium cyanate [NHi'O'CiN], although the material substrate of each of these molecular units consists of precisely the same number and kinds of atoms. Similarly, it is the atomic entelechy which gives to the isotopes of Strontium chemical properties differ- ent from those of the isotopes of Rubidium, although the mass 174 THE CASE AGAINST EVOLUTION and CM-puscular (electronic and protonic) composition of their respective atoms are identical. It is the vital entelechy or soul, which causes a fragment cut from a Stentor to regen- erate its specific protoplasmic architecture instead of the type which would be regenerated from a similar fragment cut from another ciliate such as Dileptus. In all the tridimensional units of nature, both living and non-living, the hylomorphic analysis of Aristotle recognizes an essential dualism of matter and entelechy. Hence it is not in the presence and absence of an entelechy (as Driesch con- tends) that living organisms differ from inorganic units. The sole difference between these two classes of units is one of autonomy and inertia. The inorganic unit is inert, not in the sense that it is destitute of energy, but in the sense that it is incapable of self-regulation and rigidly dependent upon ex- ternal factors for the utilization of its own energy-content. The living unit, on the other hand, is endowed with dynamic autonomy. Though dependent, in a general way, upon en- vironmental factors for the energy which it utilizes, neverthe- less the determinate form and direction of its activity is not imposed in all its specificity by the aforesaid environmental factors. The living being possesses a certain degree of inde- pendence with respect to these external forces. It is autono- mous with a special law of immanent finality or reflexive orientation, by which all the elements and energies of the living unit are made to converge upon one and the same central result, namely, the maintenance and development of the organism both in its capacity as an individual and in its capacity as the generative source of its racial type. The entelechies of the inert units of inorganic nature turn the forces of these units in an outward direction, so that they are incapable of operating upon themselves, of modifying them- selves, or of regulating themselves. They are only capable of operating upon other units outside themselves, and in so doing they irreparably externalize their energy-contents. All physi- cochemical action is transitive or communicable in character, THE ORIGIN OF LIFE 175 whereas vital action is of the reflexive or immanent type. Mechanical action, for example, is intermolar {i.e. an exchange between large masses of inorganic matter) ; physical action is intermolecular ; chemical action is interatomic ; while in radio- active and electrical phenomena we have intercorpuscular ac- tion. Hence all the forms of activity native to the inorganic world are reducible to interaction between discontinuous and unequally energized masses or particles. Always it is a case of one mass or particle operating upon another mass or particle distinct from, and spatially external to, itself. The effect or positive change produced by the action is received into another unit distinct from the agent or active unit, which can never be- come the receptive subject of the effect generated by its own activity. The living being, on the contrary, is capable of oper- ating upon itself, so that what is modified by the action is not outside the agent but within it. The reader does not modify the book, but modifies himself by his reading. The blade of grass can nourish not only a horse, but its very self, whereas a molecule of sodium nitrate is impotent to nourish itself, and can only nourish a subject other than itself, such as the blade of grass. Here the active source and receptive subject of the action is one and the same unit, namely, the living organism, which can operate upon itself in the interest of its own perfection. In chemical synthesis two substances interact to produce a third, but in vital assimilation one substance is incorporated into another without the production of a third. Thus hydrogen unites with oxygen to produce water. But in the case of assimilation the reaction may be expressed thus: Living protoplasm plus external nutriment equals living pro- toplasm increased in quantity but unchanged in specificity. Addition or subtraction alters the nature of the inorganic unit, but does not change the nature of the living unit. In chemical change, entelechy is the variant and matter is the constant, but in metabolic change, matter is the variant and entelechy the constant. ''Living beings," says Henderson, "preserve, or tend to preserve, an ideal form, while through 176 THE CASE AGAINST EVOLUTION them flows a steady stream of energy and matter which is ever changing, yet momentarily molded by life; organized, in short." ("Fitness of the Environment," 1913, pp. 23, 24.) The living unit maintains its own specific type amid a con- stant flux of matter and flow of energy. It subjugates the alien substances of the inorganic world, eliminates their min- eral entelechies and utilizes their components and energies for its ov/n purposes. The soul or vital entelechy, therefore, is more powerful than the entelechies of inorganic units which it sup- plants. It turns the forces of living matter inward, so that the living organism becomes capable of self-regulation and of striv- ing for the attainment of self-perfection. It is this reflexive orientation of all energies towards self-perfection that is the unique characteristic of the living being, and not the nature of the energies themselves. The energies by which vital functions are executed are the ordinary physicochemical energies, but it is the vital entelechy or soul which elevates them to a higher plane of efficiency and renders them capable of reflexive or vital action. There is, in short, no such thing as a special vital force. The radical difference between living and non-living units does not consist in the possession or non-possession of an entelechy, nor yet in the peculiar nature of the forces dis- played in the execution of vital functions, but solely in the orientation of these forces towards an inner finality. § 7. The Definition of Life Life, then, may be defined as the capacity of reflexive or self-perfective action. In any action, we may distinguish four things: (1) the agent, or source of the action; (2) the activity or internal determination differentiating the agent in the ac- tive state from the selfsame agent in the inactive state; (3) the patient or receptive subject; (4) the effect or change produced in the patient by the agent. Let us suppose that a boy named Tom kicks a door. Here Tom is the agent, the muscular contraction in hiis leg is the activity, the door is the patient or recipient, while the dent produced in the door is THE ORIGIN OF LIFE 177 the effect or change of which the action is a production. In this action, the effect is produced not in the cause or agent, but in a patient outside of, and distinct from, the agent, and the otherness of cause and effect is consequently complete. Such an action is termed transitive, which is the charac- teristic type of physicochemical action. In another class of actions, however, (those, namely, that are peculiar to living beings) the otherness of cause and effect is only partial and relative. When the agent becomes ultimately the recipient of the effect or modification wrought by its own activity, that is, when the positive change produced by the action remains within the agent itself, the action is called immanent or re- flexive action. Since, however, action and passion are opposites, they can coexist in the same subject only upon condition that said subject is differentiated into partial otherness, that is, organized into a plurality of distinct and dissimilar parts or components, one of which may act upon another. Hence only the organized unit or organism, which combines unity or con- tinuity of substance with multiplicity and dissimilarity of parts is capable of immanent action. The inorganic unit is capable only of transitive action, whose effect is produced in an exterior subject really distinct from the agent. The living unit or organism, however, is capable of both transitive ac- tion and immanent (reflexive) action. In such functions as thought and sensation, the living agent modifies itself and not an exterior patient. In the nutritive or metabolic function the living being perfects itself by assimilating external sub- stances to itself. It develops, organizes, repairs, and multi- plies itself, holding its own and. perpetuating its type from generation to generation. Life, accordingly, is the capacity of tending through any form of reflexive action to an ulterior perfection of the agent itself. This capacity of an agent to operate of, and upon, itself for the acquisition of some perfection exceeding its natural equilibrial state is the distinctive attribute of the living being. Left to itself, the inorganic unit tends ex- 178 THE CASE AGAINST EVOLUTION clusively to conservation or to loss, never to positive acqui- sition in excess of equilibria! exigencies; what it acquires it owes exclusively to the action of external factors. The living unit, on the contrary, strives in its vital operations to acquire something for itself, so that what it gets it owes to itself and not (except in a very general sense) to the action of external factors. All the actions of the living unit, both upon itself and upon external matter, result sooner or later in the acquisition on the part of the agent of a positive per- fection exceeding and transcending the mere exigencies of equilibration. The inorganic agent, on the contrary, when in the state of tension, tends only to return to the equilibrial state by alienation or expenditure of its energy; otherwise, it tends merely to conserve, by virtue of inertia, the state of rest or motion impressed upon it from without. In the chemical changes of inorganic units, the tendency to loss is even more in evidence. Such changes disrupt the integrity of the inorganic unit and dissipate its energy-content, and the unit cannot be reconstructed and recharged, except at the expense of a more richly endowed inorganic unit. The living organism, however, as we see in the case of the paramoecium undergoing endomixis, is capable of counteracting exhaus- tion by recharging itself. The difference between transitive and reflexive action is not an accidental difference of degree, but an essential dif- ference of kind. In reflexive actions, the source of the action and the recipient of the effect or modification produced by it are one and the same substantial unit or being. In transi- tive actions, the receptive subject of the positive change is an alien unit distinct from the unit, which puts forth the action. Hence a reflexive action is not an action which is less transitive; it is an action which is not at all transitive, but intransitive. The difference, therefore, between the living organism, which is capable of both reflexive and transitive action, and the inorganic unit, which is only capable of transi- tive action, is radical and essential. This being the case, an THE ORIGIN OF LIFE 179 evolutionary transition from an inert multimolecule to a re- flexively-operating cell or cytode, becomes inconceivable. Evo- lution might, at the very most, bring about intensifications and combinations of the transitive agencies of the physico- chemical world, but never the volte face, which would be necessary to reverse the centrifugal orientation of forces char- acteristic of the inorganic unit into the centripetal orienta- tion of forces which makes the living unit capable of self- perfective action, self-regulation, and self-renewal. The idea, therefore, of a spontaneous derivation of living units from life- less colloidal multimolecules must be rejected, not merely because it finds no support in the facts of experience, but also because it is excluded by aprioristic considerations. § 8. An Inevitable Corollary But, if inorganic matter is impotent to vitalize itself by means of its native physicochemical forces, the inevitable alternative is that the initial production of organisms from inorganic matter was due to the action of some supermaterial agency. Certain scientists, like Henderson of Harvard, while admitting the incredibility of abiogenesis, prefer to avoid open conflict with mechanism and materialism by declaring their neutrality. ''But while biophysicists like Professor Schafer," says Henderson, "follow Spencer in assuming a gradual evolu- tion of the organic from the inorganic, biochemists are more than ever unable to perceive how such a process is pos- sible, and without taking any final stand prefer to let the riddle rest." ("Fitness of the Environment," p. 310, footnote.) Not to take a decisive stand on this question, however, is tantamount to making a compromise with what is illogical and unscientific; for both logic and the inductive trend of biological facts are arrayed against the hypothesis of spon- taneous generation. In the first place, it is manifest that organic life is neither self-explanatory nor eternal. Hence it must have had its origin in the action of some external agency. Life as it exists 180 THE CASE AGAINST EVOLUTION to-day depends upon the precedence of numerous unbroken chains of consecutive cells that extend backward into a re- mote past. It is, however, a logical necessity to put an end to this retrogradation of the antecedents upon which the actual existence of our present organisms depends. The in- finite cannot be spanned by finite steps; the periodic life- process could not be relayed through an unlimited temporal distance; and a cellular series which never started would never arrive. Moreover, we do not account for the existence of life by extending the cellular series interminably back- ward. Each cell in such a series is derived from a predecessor, and, consequently, no cell in the series is self-explanatory. When it comes to accounting for its own existence, each cell is a zero in the way of explanation, and adding zeros to- gether indefinitely will never give us a positive total. Each cell refers us to its predecessor for the explanation of why it exists, and none contains within itself the sufficient expla- nation of its own existence. Hence increasing even to infinity the number of these cells (which fail to explain themselves) will give us nothing else but a zero in the way of explanation. If, therefore, the primordial cause from which these cellular chains are suspended is not the agency of the physicochemical forces of inorganic nature, it follows that the first active cause of life must have been a supermaterial and extramundane agency, namely, the Living God and Author of Life. As a matter of fact, no one denies that life has had a be- ginning on our globe. The physicist teaches that a beginning of our entire solar system is implied in the law of the de- gradation of energy, and various attempts have been made to determine the time of this beginning. The older calculations were based on the rate of solar radiation; the more recent ones, however, are based on quantitative estimates of the disintegra- tion products of radio-active elements. Similarly, the geol- ogist and the astronomer propound theories of a gradual constitution of the cosmic environment, which organic life re- quires for its support, and all such theories imply a de novo THE ORIGIN OF LIFE 181 origin or beginning of life in the universe. Thus the old nebu- lar hypothesis of Laplace postulated a hot origin of our solar system incompatible with the coexistence of organic life, which, as the experiments of Pasteur and others have shown, is destroyed, in all cases, at a temperature just above 45° Centi- grade (113° Fahrenheit). Even the enzymes or organic cata- lysts, which are essential for bio-chemical processes, are de- stroyed at a temperature between 60° and 70° Centigrade. This excludes the possibility of the contemporaneousness of protoplasm and inorganic matter, and points to a beginning of life in our solar system. Moreover, independently of this theory, the geologist sees in the primitive crystalline rocks (granites, diorites, basalts, etc.) and in the extant magmas of volcanoes evidences of an azoic age, during which tempera- tures incompatible with the survival of even the blue-green algae or the most resistent bacterial spores must have pre- vailed over the surface of the globe. In fact, it is generally recognized by geologists that the igneous or pyrogenic rocks, which contain no fossils, preceded the sedimentary or fossil- iferous rocks. The new planetesimal hypothesis, it is true, is said to be compatible with a cold origin of the universe. Nevertheless, this theory assumes a very gradual condensation of our cosmos out of dispersed gases and star dust, whereas life demands as the sine qua non condition of its existence a differentiated environment consisting of a lithosphere, a hydro- sphere, and an atmosphere. Hence, it is clear that life did not originate until such an appropriate environment was an ac- complished fact. All theories of cosmogony, therefore, point to a beginning of life subsequent to the constitution of the inorganic world. Now, it is impossible for organic life to antecede itself. If, therefore, it has had a beginning in the world, it must have had a first active cause distinct from itself; and the active cause, in question, must, consequently, have been either some- thing intrinsic, or something extrinsic, to inorganic matter. The hypothesis, however, of a spontaneous origin of life 182 THE CASE AGAINST EVOLUTION through the agency of forces intrinsic to inorganic matter is scientifically untenable. Hence it follows that life originated through the action of an immaterial or spiritual agent, namely, God, seeing that there is no other assignable agency capable of bringing about the initial production of life from lifeless matter. § 9. Futile Evasions Many and various are the efforts made to escape this is- sue. One group of scientists, for example, attempt to rid them- selves of the difficulty by diverting our attention from the problem of a beginning of organic life in the universe to the problem of its translation to a new habitat. This legerde- main has resulted in the theories of cosmozoa or panspermia, according to which life originates in a favorable environment, not by reason of spontaneous generation, but by reason of importation from other worlds. This view has been pre- sented in two forms: (1) the "meteorite" theory, which rep- resents the older view held by Thomson and Helmholtz; (2) the more recent theory of "cosmic panspermia" advocated by Svante Arrhenius, with H. E. Richter and F. J. Cohn as precursors. Sir Wm. Thompson suggested that life might have been salvaged from the ruins of other worlds and carried to our own by means of meteorites or fragments thrown off from life-bearing planets that had been destroyed by a catastrophic collision. These meteorites discharged from bursting planets might carry germs to distant planets like the earth, causing them to become covered with vegetation. Against this theory stands the fatal objection that the transit of a meteorite from the nearest stellar system to our own would require an interval of 60,000,000 years. It is incredible that life could be maintained through such an enormous lapse of time. Even from the nearest planet to our earth the duration of the journey would be 150 years. Besides, meteorites are heated to incandescence while passing through the atmosphere, and any seeds they might contain would perish by reason of the THE ORIGIN OF LIFE 183 heat thus generated, not to speak of the terrific impacts which terminates the voyage of a meteorite. Arrhenius suggests a method by which microorganisms might be conveyed through intersidereal space with far greater dispatch and without any mineral vehicle such as a meteorite. He notes that particles of cosmic dust leave the sun as a coro- nal atmosphere and are propelled through intervening space by the pressure of radiation until they reach the higher at- mosphere of the earth (viz. at a height of 100 kilometers from the surface of the latter) , where they become the electrically charged dust particles of polar auroras {v.g. the aurora borealis). The motor force, in this case, is the same as that which moves the vanes of a Crookes' radiometer. Lebedeff has verified Clerk-Maxwell's conceptions of this force and has demonstrated its reality by experiments. It is calculated that in the immediate vicinity of a luminous surface like that of the sun the pressure exerted by radiation upon an exposed surface would be nearly two milligrams per square centimeter. On a nontransparent particle having a diameter of 1.5 microns, the pressure of radiation would just counterbalance the force of universal gravitation, while on particles whose diameter was 0.16 of a micron, the pressure of radiation would be ten times as great as the pull of gravitation. Now bacterial spores hav- ing a diameter of 0.3 to 0.2 of a micron are known to bac- teriologists, and the ultramicroscope reveals the presence of germs not more than 0.1 of a micron in size.^ Hence it is con- * Recently, by means of photography with short-length light waves, the bacteria of "Foot-and-mouth disease," invisible to the highest power microscope, have been revealed as rods about 100 submicrons (i.e. 0.1 micron, or 0.0001 millimeter) in length, (c/. Science, May 30, 1924, Supplement X.) Germs of this dimension could be as easily transported by radiation as the alleged electrically charged Stardust in the aurora borealis. It may be of interest, however, to note, in this connection, that the most recent theory of the aurora borealis discards Stardust in favor of nitrogen snow. Lars Vegard, a Norwegian professor, ascribes the peculiar greenish tint in the Northern Lights to the action of solar radiations on nitrogen snow, which he assumes to exist at an altitude 184 THE CASE AGAINST EVOLUTION ceivable that germs of such dimensions might be wafted to hmits of our atmosphere, and might then be transported by the pressure of radiation to distant planets or stellar sys- tems, provided, of course, they could escape to the germicidal action of oxidation, desiccation, ultra-violet rays, etc. Ar- rhenius calculates that their journey from the earth to Mars would, under such circumstances, occupy a period of only 20 days. Within 80 days they could reach Jupiter, and they might arrive at Neptune on the confines of our solar system after an interval of 3 weeks. The transit to the constellation of the Centaur, which contains the solar system nearest to our own (the one, namely, whose central sun is the star Alpha), would require 9,000 years. Arrhenius' theory, however, that "life is an eternal rebegin- ning" explains nothing and leaves us precisely where we were. In the metaphysical as well as the scientific sense, it is an evasion and not a solution. To the logical necessity of put- ting an end to the retrogradation of the subalternate condi- tions, upon which the realities of the present depend for their actual existence, we have already adverted. Moreover, the reasons which induce the scientist to postulate a beginning of life in our world are not based on any distinctive peculiarity of that world, but are universally applicable, it being established by the testimony of the spectroscope that other worlds are not differently constituted than our own. Hence Schafer voices the general attitude of scientific men when he says: "But the acceptance of such theories of the arrival of life on earth does not bring us any nearer to a conception of its actual mode of origin ; on the contrary, it merely serves to banish the of more than 60 miles above the earth. When he condensed crystals of solid nitrogen on a copper plate by freezing with liquid hydrogen, he found that these crystals, after bombardment with cathode rays, emit a light of green color, which gives the same strong green spectrum line as the spectrum of the aurora. As the solid nitrogen evaporates, it begins to emit the reddish light characteristic of nitrogen gas. This phenomenon would explain the changes of color that occur in the aurora borealis. (c/. Science, April 18, 1924, Suppl. X.) THE ORIGIN OF LIFE 185 investigation of the question to some conveniently inaccessible corner -of the universe and leaves us in the unsatisfactory condition of affirming not only that we have no knowledge as to the mode of origin of life — which is unfortunately true — - but that we never can acquire such knowledge — which it is to be hoped is not true. Knowing what we know, and believ- ing what we believe, ... we are, I think (without denying the possibility of the existence of life in other parts of the universe), justified in regarding these cosmic theories as in- herently improbable." (Dundee Address of 1912, cf. Smith- son. Inst. Rpt. for 1912, p. 503.) Dismissing, therefore, all evasions of this sort, we may regard as scientifically established the conclusion that, so far as our knowledge goes, inorganic nature lacks the means of self-vivification, and that no inanimate matter can become living matter without first coming under the influence of mat- ter previously alive. Given, therefore, that the conditions favorable to life did not always prevail in our cosmos, it follows that life had a beginning, for which we are obliged to account by some postulate other than abiogenesis. This conclusion seems inescapable for those who concede the scien- tific absurdity of spontaneous generation, but, by some weird freak of logic, not only is it escaped, but the very opposite conclusion is reached through reasoning, which the exponents are pleased to term philosophical, as distinguished from scien- tific, argumentation. The plight of these "hard-headed wor- shippers of fact," who plume themselves on their contempt for "metaphysics," is sad indeed. Worsted in the experimental field, they appeal the case from the court of facts to that aprioristic philosophy. "Physic of metaphysic begs defence, and metaphysic calls for aid on sense!" Life, they contend, either had no beginning or it must have begun in our world as the product of spontaneous generation. But all the scientific theories of cosmogony exclude the former alternative. Consequently, not only is it not absurd to admit spontaneous generation, but, on the contrary, it is absurd not 186 THE CASE AGAINST EVOLUTION to admit it. It is in this frame of mind that August Weis- mann is induced to confide to us ''that spontaneous generation, in spite of all the vain attempts to demonstrate it, remains for me a logical necessity." ("Essays," p. 34, Poulton's Transl.) The presupposition latent in all such logic is, of course, the assumption that nothing but matter exists ; for, if the possibil- ity of the existence of a supermaterial agency is conceded, then obviously we are not compelled by logical necessity to ascribe the initial production of organic life to the exclusive agency of the physicochemical energies inherent in inorganic matter. Weismann should demonstrate his suppressed premise that matter coincides with reality and that spiritual is a synonym for nonexistent. Until such time as tliis unverified and un- verifiable affirmation is substantiated, the philosophical proof for abiogenesis is not an argument at all, it is dogmatism pure and simple. But, they protest, "To deny spontaneous generation is to proclaim a miracle" (Nageli), and natural science cannot have recourse to "miracles" in explaining natural phenomena. For the "scientist," miracles are always absurd as contra- dicting the uniformity of nature, and to recur to them for the solution of a scientific problem is, to put it mildly, distinctly out of the question. Hence Haeckel regards spon- taneous generation as more than demonstrated by the bare consideration that no alternative remains except the unspeak- able scientific blasphemy implied in superstitious terms like "miracle," "creation," and "supernatural." For a "thinking man," the mere mention of these abhorrent words is, or ought to be, argument enough. "If we do not accept the hypothesis of spontaneous generation," Haeckel expostulates, "we must have recourse to the miracle of a supernatural creation." (Italics his — "History of Creation," I, p. 348, Lankester's Transl.) It would be a difficult matter, indeed, to cram more blunders into one short sentence! We will not, and need not, undertake to defend the supernatural here. Suffice it to say, that the initiation of life in inorganic matter by the Author THE ORIGIN OF LIFE 187 of Life would not be a creation, nor a miracle, nor a phenome- non pertaining to the supernatural order. The principle of the minimum forbids us to postulate the superfluous, and a creative act would be superfluous in the production of the first organisms. Inorganic nature contains all the material elements found in living organisms, and all organisms, in fact, derive their matter from the inorganic world. If, therefore, they are thus dependent in their con- tinuance upon a supply of matter administered by the inor- ganic world, it is to be presumed that they were likewise de- pendent on that source of matter in their first origin. In other words, the material substrata of the first organisms were not produced anew, but derived from the elements of the in- organic world. Hence they were not created, but formed out of preexistent matter. A creative act would involve total production, and exclude the preexistence of the constituent ma- terial under a different form. A formative act, on the con- trary, is a partial production, which presupposes the material out of which a given thing is to be made. Hence the Divine act, whereby organic life was first educed from the passive po- tentiality of inorganic matter, was formative and not creative. Elements preexistent in the inorganic world were combined and intrinsically modified by impressing upon them a new specification, which raised them in the entitive and dynamic scale, and integrated them into units capable of self-regula- tion and reflexive action. This modification, however, was in- trinsic to the matter involved and nothing was injected into matter from without. Obviously, therefore, the production of the first organisms was not a creation, but a formation. Still less was it a miracle; for a miracle is a visible inter- position in the course of nature by a power superior to the powers of nature. A given effect, therefore, is termed miracu- lous with express reference to some existing natural agency, whose efficacy it, in some way, exceeds. If there existed in inorganic nature some natural process of self-vivification, then any Divine interposition to produce life independently 188 THE CASE AGAINST EVOLUTION of this natural agency, would be a miraculous intervention. As a matter of fact, however, inorganic nature is destitute of this power of self-vitalization, and consequently no natural agency was superseded or overridden by the initial imparting of life to lifeless matter. Life was not ordained to originate in any other way. Given, therefore, this impotence of inor- ganic nature, it follows that an initial vivification of matter by Divine power was demanded by the very nature of things. The Divine action did not come into competition, as it were, with existing natural agencies, but was put forth in response to the exigencies of nature itself. It cannot, therefore, be regarded as miraculous. Nor, finally, is there any warrant for regarding such an initial vivification of matter as supernatural. Only that is supernatural which transcends the nature, powers, and exigen- cies of all things created or creatable. But, as we have seen, if life was to exist at all, a primal animation of inanimate matter by Divine power was demanded by the very nature of things. Here the Divine action put forth in response to an exigency of nature and terminated in the constitution of living nature itself. Now, the effect of a Divine action, by which the natures of things are initially constituted, plainly pertains to the order of nature, and has nothing to do with the super- natural. Hence the primordial constitution by Divine power of living nature was not a supernatural, but a purely natural, event. CHAPTER II THE ORIGIN OF THE HUMAN SOUL § 1. Matter and Spirit We live in an age in which scientific specialization is stressed as the most important means of advancing the interests of human knowledge; and specialism, by reason of its many tri- umphs, seems to have deserved, in large measure, the prestige which it now enjoys. It has, however, the distinct disadvan- tage of fostering provincialism and separatism. This lopsided learning of the single track mind is a condition that verges on paranoia, leads to naive contempt for all knowledge not reducible to its own set of formulae, and portends, in the near future, a Babel-like confusion of tongues. In fact, the need of a corrective is beginning to be felt in many quarters. This corrective can be none other than the general and synthetic science of philosophy; it is philosophy alone that can fur- nish a common ground and break down the barriers of ex- clusiveness which immure the special sciences within the minds of experts. Scientists readily admit the advantage of philosophy in theory, but in practice their approval is far from being un- qualified. A subservient philosophy, which accepts without hesitation all the current dogmas of contemporary science, is one thing, and a critical philosophy venturing to apply the canons of logic to so-called scientific proof is quite another. Philosophy of the latter type is promptly informed that it has no right to any opinion whatever, and that only the scien- tific specialist is qualified to speak on such subjects. But the disqualification, which is supposed to arise from lack of special knowledge, is just as promptly forgotten, when there is 189 190 THE CASE AGAINST EVOLUTION question of philosophy in the role of a pliant sycophant, and the works of a Wells or a van Loon are lauded to the skies, de- spite the glaring examples of scientific inaccuracy and igno- rance, in which they abound. This partiality is sometimes carried to a degree that makes it perfectly preposterous. Thus it is by no means an infrequent thing to find scientists dismissing, as unworthy of a hearing, a philosopher like Hans Driesch, who spent the major por- tion of his life in biological research, and combined the tech- nical discipline of a scientist with the mental discipline of a logician. The chemist, H. E. Armstrong, for instance, sees in the mere label "philosopher" a sufficient reason for barring his testimony. ''Philosophers," jeers the chemist, with flippant irrelevance, ''must go to school and study in the purlieus of experimental science, if they desire to speak with authority on these matters." (Smithson. Inst. Rpt. for 1912, p. 528.) Such is his comment on Driesch, yet Driesch did nothing at all, if he did not do far more than Armstrong prescribes as a prerequisite for authoritative speaking. In James Harvey Robinson, on the contrary, we have an example of the tendency of scientists to coddle philosophers who assume a docile, deferential, and submissive attitude towards every generaliza- tion propounded in the name of natural science. In sheer gratitude for his uncritical acquiescence, his incapacitation as a nonspecialist is considerately overlooked, and he can confess, without the slightest danger of discrediting his own utterances: "I am not ... a biologist or palaeontologist. But I have had the privilege of consorting familiarly with some of the very best representatives of those who have devoted their lives to the patient study of the matters involved in this con- troversy. I think I quite understand their attitude." {Harper's Magazine, June, 1922, p. 68.) By his own testimony he is a scientific amateur, but this does not, in the least, prevent him from "speaking with authority" or from being lionized in scientific circles as an evolutionary "defender of the faith." Clearly, it is the nature of their respective views, and not the THE ORIGIN OF THE HUMAN SOUL 191 possession or absence of technical knowledge, which makes Robinsan a favorite, and Driesch a persona non grata, with "the very best representatives" of contemporary science. "Science," says a writer in the Atlantic Monthly (Oct., 1915), "has turned all philosophy out of doors except that which clings to its skirts ; it has thrown contempt on all learning that does not depend upon it; and it has bribed the sketches by giving us immense material comforts." Here, however, we are concerned with the fact, rather than the justice, of this discrimination which the scientific world makes between philosopher and philosopher. Certain it is that Robinson has received no end of encomiums from scientists, who apparently lack the literary gifts to expound their own philosophy, and that his claim to represent the views of a large and influential section of the scientific world is, in all probability, entirely correct. It is this manifest approval of scientific men which lends especial interest to the remarks of this scientific dilettante, and we shall quote them as expressing the prevalent scientific view on the origin of man, a view which, with but slight variations, has persisted from the time of Darwin down to the present day. "The recognition," says Robinson, "that mankind is a spe- cies of animal, is, like other important discoveries, illuminat- ing." {Science, July 28, 1922, p. 74.) To refer to the recog- nition of man's animality as a discovery is a conceit too stupid for mere words to castigate. Surely, there was no need of the profound research or delicate precision of modern science to detect the all too obvious similarity existing between man and beast. Mankind did not have to await the advent of an "enlightened" nineteenth, or twentieth century to be assured of the truth of a commonplace so trite and palpable. Even the "benighted" scholastics of medieval infamy had wit enough to define man as a rational animal. Indeed, it would be a libel on human intelligence to suppose that anyone, in the whole history of human thought, was ever sufficiently fatuous to dispute the patent fact that man is a sentient or- 192 THE CASE AGAINST EVOLUTION ganism compounded of flesh, blood, bone, and sinew like the brute. The "discovery" that man is a species of animal dates from the year one of human existence, and it is now high time for the novelty of this discovery to be worn off. Even as a difficulty against human superiority and immor- tality, the "recognition" is by no means recent. We find it squarely faced in a book of the Old Testament, the entire book being devoted to the solution of the difficulty in ques- tion. "I said in my heart concerning the estate of the sons of men . . . that they might see they are themselves beasts. For that which befalleth the sons of men befalleth beasts; even one thing befalleth them; as the one dieth so dieth the other; yea, they have all one breath; so that man hath no pre- eminence above a beast; for all is vanity. All go unto one place; all are of the dust, and all return to dust. Who know- eth the spirit of man whether it goeth upward, and the spirit of the beast whether it goeth downward to the earth?" {Ecclesiastes, III: 18-21.) The sacred writer insists that, so far as the body is concerned, man and the brute stand on the same level; but what of the human soul? Is it, he asks, re- solvable into matter like the soul of a beast, or is it a super- material principle destined, not for time, but for eternity? At the close of the book, the conclusion is reached that the latter alternative is the true solution of the riddle of human nature — "the dust returneth to the earth whence it was, and the spirit returneth to God who gave it." (Ch. XII, v. 7.) ' Centuries, therefore, before the Christian era, this problem was formulated by Ecclesiastes, the Jew, and also, as we shall presently see, by Aristotle, the coryphaeus of Greek philosophy. Nay, from time immemorial man, contrasting his aspirations after immortality with the spectacle of corporal death, has appreciated to the full the significance of his own animality. Never was there question of whether man is, or is not, just as thoroughly an animal as any beast, but rather of whether, his animal nature being unhesitatingly conceded, we are not, none the less, forced to recognize in him, over and above this. THE ORIGIN OF THE HUMAN SOUL 193 the existence of a spiritual mind or soul, differentiating him from the brute and constituting him a being unique, despite the unmistakable homologies discernible between bestial organisms and the human body. Everywhere and always man- kind as a whole have manifested, by the universal and uniquely human practice of burying the dead, their unswerving and indomitable conviction that man is spirit as well as flesh, an animal, indeed, yet animated by something not present in the animal, namely, a spiritual soul, deathless and inde- structible, capable of surviving the decay of the organism and of persisting throughout eternity. But, if the human mind or soul is spiritual, it is clear that it cannot be a product of organic evolution, any more than it can be a product of parental generation. On the contrary, each and every human soul must be an immediate creation of the Author of Nature, not evolved from the internal poten- tiality of matter, but infused into matter from without. The human soul is created in organized matter, but not from it. Nor can the Divine action, in this case, be regarded as a supernatural interposition; for it supplements, rather than supersedes, the natural process of reproduction; and, since it is not in matter to produce spirit, a creative act is demanded by the very nature of things. Evolution is nothing more nor less than a transmutation of matter, and a transmutation of matter cannot terminate in the annihilation of matter and the constitution of non-mat- ter or spirit. If nothing of the terminus a quo persists in the final product, we have substitution, and not transmutation. The evolution of matter, therefore, cannot progress to a point where all materiality is eliminated. Hence, whatever proceeds from matter, either as an emanation or an action, will, of necessity, be material. It should be noted, however, that by material we do not mean corporeal; for material denotes not merely matter itself, but everything that intrinsically depends on matter. The term, therefore, is wider in its sense than corporeal, because it comprises, besides matter, all the prop- 194 THE CASE AGAINST EVOLUTION erties, energies, and activities of matter. Hence whatever is incapable of existence and activity apart from matter (whether ponderable or imponderable) belongs to the material, as dis- tinguished from the spiritual, order of things. The soul of a brute, for example, is not matter, but it is material, never- theless, because it is totally dependent on the matter of the organism, apart from which it has neither existence nor activity of its own. In the constitution of the sentient or animal soul, matter reaches the culmination of its passive evolution. True, its inherent physicochemical forces do not suffice to bring about this consummation, wherewith its internal potentiality is exhausted. Nevertheless, the emergence of an animal soul from matter is conceivable, given an agency competent to educe it from the intrinsic potentiality of matter; for, in the last analysis, the animal soul is simply an internal modification of matter itself. But, if spirit is that which exists, or is, at least, capable of existence, apart from matter, it goes with- out saying that spirit is neither derivable from, nor resolv- able into, matter of any kind. Consequently, it cannot be evolved from matter, but must be produced in matter by cre- ation {i.e. total production). To make the human mind or soul a product of evolution is equivalent to a denial of its spirituality, because it implies that the human soul like that of the brute, is inherent in the potentiality of matter, and is therefore a purely material principle, totally dependent on the matter, of which it is a perfection. Between such a soul and the sentient principle present in the beast, there would be no essential difference of kind, but only an accidental dif- ference of degree; and this is precisely what Darwin and his successors have spared no effort to demonstrate. James Har- vey Robinson is refreshingly frank on this subject, and we will therefore let him be spokesman for those who are more reticent: "It is the extraordinarily illuminating discovery {sic) of man's animalhood rather than evolution in general that THE ORIGIN OF THE HUMAN SOUL 195 troubles the routine mind. Many are willing to admit that it looks- as if life had developed on the earth slowly, in suc- cessive stages; this they can regard as a merely curious fact and of no great moment if only man can be defended as an honorable exception. The fact that we have an animal body may also be conceded, but surely man must have a soul and a mind altogether distinct and unique from the very begin- ning bestowed on him by the Creator and setting him off an immeasurable distance from any mere animal. But what- ever may be the religious and poetic significance of this compromise it is becoming less and less tenable as a scientific and historic truth. The facts indicate that man's mind is quite as clearly of animal extraction as his body." {Science^ July 28, 1922, p. 95— italics his.) This language has, at least, the merit of being unambiguous, and leaves us in no uncertainty as to where the writer stands. It discloses, likewise, the animus which motivates his peculiar interest in transformistic theories. If evolution were incapable of being exploited in behalf of materialistic philosophy, Mr. Robinson, we may be sure, would soon lose interest in the theory, and would once more align himself with the company, which he has so inappropriately deserted, namely, ''the routine minds" that regard evolution "as a merely curious fact of no great moment." Be that as it may, his final appeal is to the "facts," and it is to the facts, accordingly, that we shall go; but they will not be the irrelevant "facts" of anatomy, physi- ology, and palaeontology. Sciences such as these confine their attention to the external manifestations of human life, and can tell us nothing of man's inner consciousness. It does not, therefore, devolve upon them to pronounce final judgment upon the origin of man. For that which is the distinguishing characteristic of man is not his animal nature, that he shares in common with the brute, but his rational nature, which alone differentiates him from "a beast that wants discourse of reason." We cannot settle the question as to whether or not man's mind is "of animal extraction" by comparing his body 196 THE CASE AGAINST EVOLUTION with the bodies of irrational vertebrates. To institute the requisite comparison between the rational mentality of man and the purely sentient consciousness of irrational animals falls within the exclusive competence of psychology, which studies the internal manifestations of life as they are presented to the intuition of consciousness, rather than biology, which studies life according to such of its manifestations as are per- ceptible to the external senses. Hence it is within the domain of psychology alone, that man can be studied on his distinc- tively human, or rational, side, and it is to this science, accord- ingly, that we must turn in our search for facts that are germane to the problem of the origin of man and the genesis of the human mind. How little, indeed, does he know of human nature, whose knowledge of it is confined to man's insignificant anatomy and biology, and who knows nothing of the triumphs of human genius in literature, art, science, architecture, music, and a thousand other fields! Psychology alone can evaluate these marvels, and no other science can be of like assistance in solving the problem of whether man is, or is not, unique among all his fellows of the animal kingdom. § 2. The Science of the Soul As a distinct science, psychology owes its origin to Aristotle, whose ^'PeH Psyches^' is, in all probability, the first formal treatise on the subject. Through his father, Nichomachus, who was court physician to Philip of Macedon, he became ac- quainted, at an early age, with biological lore in the form of such medical botany, anatomy, and physiology as were com- monly known in prescientific days. Subsequently, his cel- ebrated pupil, Alexander the Great, placed at his disposal a vast library, together with extensive opportunities for bio- logical research. This enabled the philosopher to criticize and summarize the observations and speculations of his predeces- sors in the field, and to improve upon them by means of per- sonal reflection and research. In writing his psychology, he was naturally forced to proceed on the basis of the facts dis- THE ORIGIN OF THE HUMAN SOUL 197 coverable by internal experience (introspection) and unaided external: observation. Of such facts as are only accessible by means of instrumentation and systematic experimentation, he could, of course, know nothing, since their exploration awaited the advent of modem mechanical and optical inventions. But the factual foundation of his treatise, though not extensive, was solid, so far as it went, and his selection, analysis, and evaluation of the materials at hand was so accurate and judicious, that the broad outlines of his system have been vin- dicated by the test of time, and all the results of modem ex- perimental research fit, with surprising facility, into the frame- work of his generalizations, revision being nowhere necessary save in nonessentials and minor details. Wilhelm Wundt, the Father of Experimental Psychology, pays him the following tribute: "The results of my labors do not square with the ma- terialistic hypothesis, nor do they with the dualism of Plato or Descartes. It is only the animism of Aristotle which, by combining psychology with biology, results as a plausible metaphysical conclusion from Experimental Psychology." ("Grundzuge der physiologischen Psychologie," 4t€ Auflage, II, C. 23, S. 633.) Literally translated, the title of Aristotle's work signifies a treatise concerning the soul. It set a precedent for the scholastic doctors of the thirteenth century, and de anima be- came with them a technical designation for all works dealing with this theme. In the sixteenth century the selfsame usage was embalmed in the Greek term psychology, which was coined with a view to rendering the elliptic Latin title by means of a single word. Melanchthon is credited with having originated the term, which, in its original use as well as its etymology, denoted a science of the 'psyche or soul. Towards the close of the seventeenth century, however, the meaning of the term in question began to undergo a marvelous evolution, of which the end is not yet. The process was ini- tiated by Descartes, under whose auspices psychology was changed from a science of the soul into a science of the mind. M THE CASE AGAINST EVOLUTION Then, under the influence of Hume and Kant, the noumenal mind disappeared, leaving only phenomenal consciousness. Recently, with the advent of Watson, even consciousness it- self has been discarded and psychology has become a science of behavior. And here, for the time being, at any rate, the process has come to a stop, just one step short of complete nihilism. Woodworth quotes the following waggish comment: 'Tirst psychology lost its soul, then it lost its mind, then it lost consciousness; it still has behavior of a kind." ("Psychology, the Science of Mental Life," p. 2, footnote.) This gradual degeneration of psychology from animism into behaviorism is one of the greatest ironies in the history of human thought. All of this, however, was latent in the corrosive Cartesian principle of "scientific doubt." Facilis descensus Avernil It is easy to question the validity of this or that kind of human knowledge, but difficult to arrest, or even foresee, the conse- quences which the remorseless logic of scepticism portends. Disintegration set in, as has been said, when Descartes substituted his psychophysical dualism of mind and matter for Aristotle's hylomorphic dualism of soul and body. The French philosopher, in an appendix to his "Meditations," which dates from 1670, expressly rejects the Aristotelian term of soul or psyche, and announces his preference for mind or spirit, in the following words: "The substance in which thought immediately resides is here called mind (mens, esprit). I here speak, however, of mens (mind) rather than anima (soul), for the latter is equivocal, being frequently applied to denote what is material" ("Reply to the Second Objections," p. 86). Henceforth psychology ceased to be a science of the soul, and became, instead, a science of the mind. Descartes, one must bear in mind, divided the universe into two great realms of being, namely: the conscious and the unconscious, the psychic world of mind and the physical world of matter, unextended substance which thinks and ex- tended substance which moves. In man these two substantial principles were conceived as being united by the tenuous link THE ORIGIN OF THE HUMAN SOUL 199 of mere contact, the spirit or mind remaining separate from, and unmingled with, its material partner, the body. The main trouble with this dualism is that it draws the line of de- marcation at the wrong place. Reason and sense-conscious- ness are bracketed together above the line as being equally spiritual; physiological processes and processes purely physico- chemical are coupled below the line as being equally mechani- cal. Now, when a brain-function such as sense-perception is introduced, like another Trojan Horse, into the citadel of spiritualism, it is a comparatively easy task for materialism to storm and sack that citadel by demonstrating with a thou- sand neuro-physiological facts that all sensory functions are rigidly correlated with neurological processes, that they are, in short, functions of the nervous system, and therefore purely material in nature. On the other hand, once we re- treat from the trench of distinction between the processes of unconscious or vegetative life and the physicochemical proc- esses of the inorganic world, that moment we have lost the strategic position in the conflict with mechanism, and nothing avails to stay its triumphant onrush. Hence, from first to last, it is perfectly clear that the treacherous psychophysical dualism of Descartes has done far more harm to the cause of spiritualism than all the assaults of materialism. There is a Latin maxim which says: Extrema sese tangunt — "Extremes come in contact with each other." The ultraspiritualism of Descartes by confounding spiritual, with organic conscious- ness, leads by the most direct route to the opposite extreme of crass materialism. Aristotle's dualism of matter and form, which is but a phys- ical application of his transcendental dualism of potency (dynamis) and act (entelechy), is very different from the Cartesian dualism of the physical and the psychic. According to the Aristotelian view, as we have seen in the last chapter, all the physical entities or substantial units of nature (both living and inorganic) are fundamentally dual in their essence, each consisting of a definitive principle called entelechy and 200 THE CASE AGAINST EVOLUTION a plastic principle called matter. Entelechy is the integrating determinant, the source of the unit's coherence and of its dif- ferentiation from units of another type. Matter is the de- terminable and quantifying factor, in virtue of which the unit is potentially-multiple and endowed with mass. In the electro- chemical reactions of non-living substances (synthesis, analy- sis, and transmutation), entelechy is the variant and matter is the constant; in the metabolic activities of living substances (assimilation and dissimilation), matter is the variant and entelechy is the constant. This persistent entelechy of the living unit or organism is what Aristotle terms the psyche or soul. The latter, therefore, may be defined as the vital prin- ciple or primary source of life in the organism. But in using such terms as "soul" and "vital principle" we are employing expressions against which not merely rabid mechanists, but many conservative biologists as well, see fit to protest. The opposition of the latter, however, is found on closer scrutiny to be nominal rather than real. It is the name which offends; they have no objection to the thing sig- nified. Wilson, to cite a pertinent example, rejects as meaning- less all such terms as "vital principle," "soul," etc. "They are words," he avers, "that have been written into certain spaces that are otherwise blank in our record of knowledge, and as far as I can see no more than this." ("Biology," p. 23, 1908.) Yet he himself affirms again and again the existence of the reality which these terms (understood in their Aris- totelian sense) denote. In discussing the relation of the tissue cell to the multicellular body, for instance, he speaks of "a formative power pervading the growing mass as a whole." ("The Cell," 2nd ed., p. 59), and, in his recent lecture on the "Physical Basis of Life," he makes allusion to "the in- tegrating and unifying principle in the vital processes." (Science, March 9, 1923, p. 284.) It would seem, therefore, that Wilson's aversion to such terms as soul and vital prin- ciple is based on the dynamic sense assigned to them by the neo-vitalists, who, as we have seen, regard the vital principle THE ORIGIN OF THE HUMAN SOUL 201 as a force sui generis or a unique agent, which operates in- trusively among physicochemical factors in the role of an active or efficient cause of vital functions. That such is really the case, appears from his rhetorical question: "Shall we then join hands with the neo-vitalists in referring the unifying and regulatory principle to the operation of an imknown power, a directive force, an archaeus, an entelechy or a soul?" {Loc. cit., p. 285 — italics mine.) The objection, however, does not apply to these terms used in their Aristotelian sense. In the phi- losophy of the Stagirite, the soul, like all other entelechies, is a cause in the entitive, but not in the dynamic, order of things. Its efficacy is formal, not efficient. It is not an agent, but a specifying type. The organism must be integrated, specified, and existent before it can operate, and hence its integration and specification by the soul is prior to all vital activity. The soul is a constituent of being and not an immediate principle of action. The soul is not even an entity (in the sense of a complete and separate being) , but rather an incomplete entity or constituent of an entity. It takes a complete entity to be an agent, and the soul or vital entelechy is not an independent existent, which is somehow inserted into the organism, but an incomplete being which has no existence of its own, but only co- existence, in the composite that it forms with the organism. Nor is there any such thing as a special vital force resident in the organism. The executive factors in all vital operations of the organic order are the physicochemical energies, which are native to matter in general. These forces, as we have seen, receive a reflexive orientation and are elevated to a higher plane of efficiency by reason of their association with an en- telechy superior to the binding and type-determining principles present in inorganic units, but they are not supplanted or superseded by a new executive force. Wilson's fear, therefore, that the experimental analysis of life is discouraged by vital- ism, inasmuch as this conception subtracts something from, the efficiency of the physicochemical forces, is groundless in the case of hylomorphic vitalism., but is well-founded in the 202 THE CASE AGAINST EVOLUTION case of such systems as the neo-vitalism of Driesch and the spiritualism of Descartes. Summing up, therefore, we may say that the soul, like other entelechies, is consubstantial with its material substrate, the body. True it is more autonomous than are the inflexible entelechies of inorganic nature, inasmuch as it is independent of any given atom, molecule, or cell in the organic aggregate. Such a degree of freedom, for example, is not possessed by the most complex molecules, which show no other flexibility than tautomerism, even this small readjustment involving a change in their specificity. But this autonomy does not pre- clude the essential dependence of the soul upon the body. Generally speaking, the soul is incapable of existence apart from its total substrate, the organism. We say, generally speaking, because, as previously intimated, an exception must be made in the case of the human soul, which, being, as we shall see, a self-subsistent and spiritual entelechy, is by itself, apart from its material substrate, a sufficient subject of existence, and is therefore capable of surviving the dissolution of its complementary principle, the organism. Nevertheless, even in man, the soul forms one substance with the organism, and the organism participates as a coefficient factor in all his vital functions, both physiological and psychic, excluding only the super organic or spiritual functions of rational thought and volition, whose agent and recipient is the soul alone. In man, then, soul and body unite to form a single substance, a single nature, and a single person. Apart from the body, the human soul is, indeed, a complete entity, in the sense that it is capable of subsistence (independent existence) , but, in another sense, it is not a complete entity, because apart from the body it cannot constitute a complete nature or complete per- sonality. It is this essential incompleteness of the discarnate human soul that forms the natural basis of the Christian doctrine of the Resurrection of the Dead. Here, however, it is important to note the difference be- tween the hylomorphic spiritualism of Aristotle and the psy- THE ORIGIN OF THE HUMAN SOUL 203 chophysical spiritualism of Descartes. By the latter all con- scious or physic functions are regarded as spiritual. The for- mer, however, recognizes the fundamental difference which exists between the lower or animal, and the higher or rational functions of our conscious life. Sense-perception and sensual emotion belong to the former class, and must be regarded as organic functions, whose agent and subject is neither the soul alone nor the organism alone, but the soul-informed organism or substantial composite of body and soul. Rational thinking and willing, on the contrary, are classified as superorganic or spintual functions, inasmuch as they exclude the coagency of the organism and have the soul alone for their active cause and receptive subject. The soul, in fine, is the formal principle or primary source of the threefold life in man, namely, the metabolic life, which man shares with plants, the sentient life, which he shares with animals, and the rational life, which is uniquely human. The human soul is often spoken of as the mind. In their dictionary sense, both terms denote one and the same reality, namely, the human entelechy or vital principle in man, but the connotation of these terms is different. The term soul signifies the vital principle in so far as it is the primary source of every kind of life in man, that is, vegetative, sentient, and rational. The term mind, however, connoting conscious rather than uncon- scious life, signifies the vital principle in so far as it is the root and ground of our conscious life (both sentient and rational). Here, however, the distinction is of no great moment, and the terms may be regarded as synonymous. The definitions which we have given are, of course, blasphemous in the ears of our modern neo-Kantian phenomenalists, whose preference is for a functional, rather than a substantial, mind or soul; but we will pay our respects to them later. It is clear, however, from what has been said, that, for evidences of the superiority and spirituality of the human soul, we must recur, not to the external manifestations of our nu- tritive life, but to the internal manifestations of our conscious 204 THE CASE AGAINST EVOLUTION life. The latter are wholly inaccessible to the external senses and perceptible only to the intuition of consciousness, intro- spection, or internal experience, as it is variously called. All our self-knowledge rests on the basis of introspection, and without it the science of psychology would be impossible. In fact, not only psychology, but the physical sciences as well, depend for their validity on the testimony of consciousness; for the external world is only knowable to the extent that it enters the domain of our consciousness. Recently, as we have seen, a tendency to discredit internal experience has arisen among materialistic extremists. This "tendency," to quote the words of Keyser, "most notably represented by the behaviorist school of psychologists (like Professor Watson, for example), is manifest in the distrust of introspections as a means of knowledge of mental phenomena and in the growing depend- ence of psychology upon external observation of animal and human behavior and upon physiological experiment, as if mat- ter were regarded 'as something much more solid and indubi- table than mind' (Bertrand Russell)." — C. J. Keyser, Science^ Nov. 25, 1921, p. 520. Since, however, all our knowledge de- pends on the validity of consciousness, such a tendency is suicidal and destructive of all science, whether physical or psychological. The attempts, therefore, of mechanists, like Loeb, and behaviorists, like Watson, to dispense with con- sciousness overreach themselves. For how can the mechanists know that there are such things as tropisms, tactisms, or reaction-systems, how can the behaviorist study such things as "situations," "adjustments," and S-R-bonds, how can the materialist become aware of the existence of molecules and atoms, except through the medium of their own conscious or psychic states? States of matter can be known only by means of states of mind, and the former, therefore, cannot be any more real than the latter. "What, after all," asks Cardinal Mercier, "is a fact of nature if the mind has not seized, examined, and assimilated it? True, the information of con- sciousness is often precarious. For this reason we do well to THE ORIGIN OF THE HUMAN SOUL 205 aid and control it by scientific apparatus. These apparatus, however, can only aid, never supplant, introspection. The telescope does not replace the eye, but extends its vision." ("Relation of Exp. Psych, to Philosophy," pp. 40, 41 — Trans. of Wirth.) § 3. Tlie Nature of the Human Soul Now our inner consciousness bears unmistakable witness to the existence within us of an abiding subject of our thoughts, feelings, and desires. In biology, the soul is revealed to us as a binding-principle, that obstructs dissolution of the organ- ism, and a persistent type that maintains its identity amid an incessant flux of matter and flow of energy. Clearer still is testimony of introspective psychology, which reveals all our psychic activities and states as successive modifications of this permanent "I," "self," "personality," or "mind," according as we choose to express it. Human language proves this most forcibly; for the intramental facts and data of our conscious life simply cannot be so much as intelligibly expressed, much less, defined, or differentiated from the extramental facts of the physical world, without using terms that include a reference to this selfsame persistent subject of thought, feeling, and voli- tion. Even inveterate phenomenalists, like Wundt, James, and Titchener, are obliged to submit to this inexorable linguistic law, in common with their unscientific brethren, the generality of mankind, although they do so only after futile attempts at a "scientific revision" of grammar, and with much grumbling over the "barbarous conceptions" of the gross-headed aborig- ines who invented human language. Be that as it may, no formulation of mental facts is possible except in terms that either denote or connote this permanent source and ground of human thought and feeling, as is apparent, for example, from such phrases as: "/ think," "/ wish," "/ hear"; '^mental states" (i.e. of the mind) ; psychic functions [i.e. of the psyche) ; subjective idealism (i.e. of the subject) ; a conscious act (from con-scire: "to know along with," because in 206 THE CASE AGAINST EVOLUTION conscious acts the subject is known along with the object). The phenomenalists occasionally succeed, in their "most pre- cise" passages, in omitting to mention the person, knower, or thinker behind thought, but they do so only at the cost of sub- stituting personal pronouns, and of thus bringing back through the window what they have just ejected by way of the door. Our consciousness, therefore, makes us invincibly aware of the existence of a superficially variable, but radically unchange- able, subject of our mental life. It does not, however, tell us anything concerning the nature of this primary ground of thought, whether, for example, it is identical with the cerebral cortex, or something distinct therefrom, whether it is phenome- nal or substantial, dynamic or entitive, spiritual or material. To decide these questions the unanalyzed factual data of internal experience do not suffice, but they do suffice to estab- lish the reality of the ego or subject of thought. Later we shall see that the analysis of these data, when taken in con- junction with other facts, forces us to predicate of the soul such attributes as substantiality, simplicity, and spirituality, but here they are cited solely for their factual force and not for their logical implications. The phenomenalistic schools of Interactionism and Psycho- physical Parallelism deny the substantiality of the soul, and seek to resolve it into sourceless and subjectless processes. A phenomenal mind or soul, however, could not be the primary ground of mental life, for the simple reason that phenomena presuppose a supporting medium (otherwise they would be self-maintaining, and therefore, substantial). Now that which presupposes cannot be a primary principle, but only a sec- ondary^, or tertiary principle. Consequently, a functional mind could not be the primary and irreducible ground of mental life, but only that of which it is a function, whether that some- thing is a material, or a spiritual substance. For the present, we are not interested in the nature of this ultimate substrate, we are content with the fact that it really exists. Phenomenal- ists (like Wundt, Paulsen, and James) are very inconsistent THE ORIGIN OF THE HUMAN SOUL 207 when they admit material molecules as the extended substrate of extramental or physical phenomena, while denying the ex- istence of the mind or ego as the inextended substrate of intramental or psychic phenomena. All substance, whether material or spiritual, is inaccessible to the senses. Even ma- terial substrates are manifested only by their phenomena, being in themselves supersensible and "metaphysical." If, then, the human understanding is inerrant in ascribing a material substrate to extramental phenomena, then it is equally inerrant in attributing to intramental phenomena the intimate substrate called mind, whether this substrate be a spiritual substance, or a material substance like the sub- strate of physical phenomena and that of organic life. As a matter of fact, the Psychophysical Parallelists actually do reduce mental phenomena to a material substrate (viz. the cerebral cortex). Their phenomenalism, which we will refute presently, is but a disingenuous attempt to gloss over their fundamental materialism. At all events, they are willing to admit an ultimate substantial ground of thought and volition, provided it is not claimed that this substrate is of a spiritual nature. The bare existence of some substrate, however, is all that we assert, for the present. Before leaving this topic, we wish to call attention to the fact that the subject of thought and desire is active as well as passive. Mind, in other words, is not merely a persistent me- dium wherein passive mental states are maintained, but an active and synthetic principle as well. Mental processes, like those of judgment, reasoning, and recognition, require a unitary and unifying principle, which actively examines and compares our impressions and thoughts, in order to discern their rela- tions to one another and to itself. Materialistic psychology, in spite of the plain testimony of consciousness, is all for ig- noring the mind in its active role as the percipient of the iden- tities and discrepancies of thought, and for regarding mind as a mere complex of mental states or transient flux of fleeting imagery. It is well, then, to bear in mind the indubitable 208 THE CASE AGAINST EVOLUTION facts of internal experience, to which Cardinal Mercier calls attention. "English psychology," he observes, "had attempted a kind of anatomy of consciousness. It made all consist in passive sensations or impressions. These impressions came to- gether, fused, dissociated under the guidance of certain laws, principally those of similarity and dissimilarity. The whole process was entirely passive without the intervention of any active subject. It was psychology without a soul. Now that things are being examined a little more closely, psychologists find that there are a lot of conscious states that are without the slightest doubt active on the part of the subject. There are a number of mental states upon which the subject brings his attention to bear, and attention (from ad-tendere) means activity. Ordinarily we do not know the intensity of a sensa- tion without comparing it with another preceding one. This work of comparison, or, as the English call it, discrimination, is necessarily activity. The Associationists had confounded the fact of coexistence with the perception of similarity or dissimilarity. Supposing even that the coexistence of two mental states were entirely passive, it still remains true that the notion of their similarity or dissimilarity requires an act of perception. It is absolutely impossible to conceive psychical life without an active subject which perceives itself as living, notes the impressions it receives, compares its acts, associates and dissociates them; in a word, there can be no psychology without a perceiving subject which psychologists call esprit, or with the English, 'mind.' " {Op. cit., pp. 52-54 — italics his.) The conflict between phenomenalism and the clear testimony of consciousness is summed up in the following words of T. Fontaine: "If all things are phenomena, then we ourselves can be nothing more than events unknown to one another; in order, then, that such events may appear to us united, so that we may be able to declare their succession within us, it is necessary that something else besides them should exist; and this something else, this link that binds them together, this principle that is conscious of their succession, can be THE ORIGIN OF THE HUMAN SOUL 209 nothing else than a non-event or non-phenomenon, namely, a substance, an ego substantially distinct from sensations." ("La sensation et la pensee," p. 23.) For the phenomenalists, mind is but a collective term for the phenomenal series of our transitory thoughts and feelings. With Wundt, they discard the substantial or entitive soul for a dynamic or functional one, ''die aktuelle Seele" (Cf. Grundz. der Phys. Psych., ed. 5th, III, p. 758 et seq.) Thought antecedes itself by becoming its own thinker; for Titchener tells us : "The passing thought would seem to be the thinker." ("Pr. of Psych.," I, p. 342.) We do not think, but thought thinks ; John does not walk, but walking walks ; aero- planes do not fly, but flight flies; air does not vibrate, but vibration vibrates. The phenomenalist objectivates his sub- jective abstractions, divorces processes from their agents, and substantializes phenomena. The source of his error is a con- fusion of the ideal, with the real, order of things. Because it is possible for us to consider a thought apart from any determinate thinker, by means of a mental abstraction, he very falsely concludes that it is possible for a thought to exist without a concrete thinker. It would be obviously absurd to suppose that the so-called Grignard reaction could occur without definite reactants, merely because we can think of it without specifying any particular kind of alkyl halide; it would be preposterous to infer, from the fact that vibration can be considered independently of any concrete medium such as air, water, or ether, that therefore a pure vibration can exist without any vibrating medium; and it is equally absurd to project an abstraction like subjectless thought into the realm of existent reality. Abstractions are ideal entities of the mind; they can have no real existence outside the domain of thought. Hence to assign a real or extralogical existence to actions, modalities, and properties, in isolation from the concrete sub- jects, to which they belong, is a procedure that is not legiti- mate in any other world than Alice's Wonderland, where, we are told, the Cheshire Cat left behind his notorious grin long 210 THE CASE AGAINST EVOLUTION after his benign countenance had faded from view. His face- less grin is a fitting comment on the neo-Kantian folly of those who, as L. Chiesa says, "speak of phenomena without substance, of sensations without subject, of thoughts without the Ego, to which they belong, imitating in this way the poets, who personify honor, virtue, beauty, etc. Now all this pro- ceeds exclusively from a confusion of the subjective abstrac- tion with the reality, and from the assumption that the phe- nomenon, for example, exists without substance, because we are able (by means of abstraction) to consider the former independently of the latter." ("La Base del Realismo," p. 39.) In other words, the mind is capable of separating (represen- tatively, of course, and not physically) its own phenomena from itself, but this is no warrant for transferring the abstrac- tions thus formed from the ideal, to the real, order of things. So much for the soul's substantiality, but it is a simple, as well as a substantial, principle, that is to say, it is inextended, uncompounded, incorporeal, and not dispersed into quantita- tive parts or particles. In other words, it is not a composite of constituent elements or complex of integral parts, but something really distinct from the body and pertaining to a different order of reality than matter. This, as we have seen, does not necessarily mean that it is immaterial, in the sense of being intrinsically independent of matter. In a word, sim- plicity does not involve spirituality (absolute immateriality). Not only plant and animal souls, but even mineral entelechies, are simple, in the negative sense of excluding extension, cor- poreality and dispersal into quantitative parts, but they are, none the less, intrinsically dependent on matter and are therefore material principles. That the soul or vital entelechy is really distinct from its material substrate is apparent from the perennial process of metabolism enacted in the living organism. In this process, matter is the variant and entelechy or specific type is the constant. Hence the two principles are not only distinct, but separable. Moreover, the soul's role as a binding-principle THE ORIGIN OF THE HUMAN SOUL 211 that obstructs dissolution is incompatible with its dispersal into quantitative parts; for such a principle, far from being able to bind, would require binding itself, and could not, therefore, be the primary source of unification in the or- ganism. Finally, the soul must be incorporeal; since, if it were a corporeal mass, it could not be "a formative power pervading the growing mass as a whole" (Wilson) ; for this would involve the penetration of one body by another. Con- sequently, the soul is a simple, inextended, incorporeal reality undispersed into quantitative parts. Introspective psychology bears witness to the same truth; for consciousness reinforced by memory attests the substan- tial permanence of our personal identity. We both think and regulate our practical conduct in accordance with this sense of unchanging personal identity. All recognition of the past means simply this, that we perceive the substantial identity of our present, with our past, selves throughout all the ex- periences and vicissitudes of life. There is an inmost core of our being which is unchanging and which remains always identical with itself, in spite of the flow of thought and the metabolic changes of the life-cycle. It is this that gives us the sense of being always identically the same person, from infancy to maturity, and from maturity to old age. It is this that constitutes the thread of continuity which links our yesterdays with to-day, and makes us morally responsible for all the deliberate deeds of a lifetime. Courts of law do not acquit a criminal because he is in a different frame of mind from that which induced him. to commit murder, nor do they excuse him on the score that metabolism has made him a different mass of flesh from that which perpetrated the crime. Such philosophies as phenomenalism and materialism are purely academic. Even their advocates dare not reduce them to consistent practice in everyday life. Nor can the cases of alternating personalities be adduced as counterevidence. In the first place, these cases are psycho- pathic and not normal. In the second, they are due, not to a 212 THE CASE AGAINST EVOLUTION modification of personality itself, but to a modification in the perception of personality. Since this perception is, as we shall see, extrinsically dependent on cerebral imagery, any neuropathic affection is liable to modify the perception of per- sonality by seriously disturbing the imagery, on which it depends. But {pace Wundt and James) the perception of personality is one thing, and personality itself quite another. Perception does not produce its objects, but presupposes them, and self-perception is no exception to this rule. Introspec- tion, therefore, does not create our personality, but reveals and represents it. If then to the intuition of consciousness our per- sonality appears as an unchanging principle that remains always substantially identical with itself, it follows that this perception must be terminated by something more durable than a flux of transient molecules or a stream of fleeting thought. Unless this perceptive act has for its object some unitary and uniformly persistent reality distinct from our com- posite, corruptible bodies, and not identified with our tran- sitory thoughts, this sense of permanent personal identity would be utterly impossible. Materialism, which recognizes nothing more in man than a decaying organism, a mere vortex of fluent molecules, is at a loss to account for our conscious- ness of being always the same person. Phenomenalism, which identifies mind or self with the "thought-stream," is equally impotent to account for this sense of our abiding sameness. James' attempt at a phenomenalistic explanation of the persistent continuity of self, on the assumption that each passing thought knows its receding predecessor and be- comes known, in turn, by its successor, is puerile. To pass over other flaws, this absurd theory encounters an insuperable difficulty in sleep, which interrupts, for a con- siderable interval, the flow of conscious thought. Thought is a transient reality, which passes, so far as its actuality is concerned, and can only remain in the form of a permanent effect. Unless, therefore, there were some persistent medium in which the last waking thought could leave a permanent THE ORIGIN OF THE HUMAN SOUL 213 vestige of itself, the process of relaying the past could never be resumed, and we would lose our personal identity every twentj'-four hours. The mind, or subject of thought, then, must be an abiding and unitary principle distinct from our composite bodies, and from our manifold and fleeting thoughts. Finally, to the two foregoing attributes of the human soul (substantiality and simplicity), we must add a third and crowning attribute, namely, spirituality. It is this, and this alone, that differentiates the human from the bestial soul, which latter is but an incomplete complement of matter, in- capable of existence apart from matter, and doomed to perish with the dissolution of the organism, as the cylindrical form of a candle perishes with the consumption of the wax by the flame. All the psychic activities of the brute, such as sensation, object-perception, imagination, associative memory, sensual emotion, etc., are organic functions of the sensitivo-nervous type. In all of them the agent and recipient is not the soul alone, but the psycho-organic composite of soul and organism, that is, the soul-informed sensory and central neurons of the cerebrospinal system. The sensory neurons are nerve cells that transmit centerward the excitations of physical stimuli received by the external sense organs or receptors, in which their axon-fibers terminate. These receptors and sensory neurons are extended material organs proportioned and spe- cialized for receiving physical impressions from external bodies, either directly through surface-contact with the bodies themselves or their derivative particles {e.g. in touch, taste and smell), or indirectly through surface-contact with an extended vibrant medium such as air, water, or ether (e.g. in hearing and sight). The central neurons of the cerebral cortex are, as it were, the tablets, upon which the excitations transmitted thither by the sensory neurons, record the ex- tended neurograms that constitute the physical basis of the concrete imagery of memory and imagination. Interior senses, 214 THE CASE AGAINST EVOLUTION then, like memory and imagination, merely continue and combine what was preexistent in the exterior senses. Their composite imagery is rigidly proportioned to the extended neurograms imprinted on the cerebral neurons, and these neurograms, in turn, are determined both qualitatively and quantitatively by the physical impressions received by the receptors, and these impressions, finally, are exactly propor- tioned to the action of the material stimuli in contact with the receptors. Thus the composite images of imagination as well as those of direct perception are proportioned to the underlying neurograms of the cortex and correspond exactly, as regards quality, intensity, and extensity, to the original stimulus af- fecting the external receptors. Hence men born blind can never imagine color, nor can men born deaf ever imagine sound. An inextended principle, such as the discarnate soul, cannot receive or record impressions from extended vibrant media, or from extended corporeal masses. For this the soul requires the intrinsic cooperation of material receptors. Now, the highest cognitive and appetitive functions of the brute {e.g. sense-per- ception and emotion) are, as has been stated, of the sensitivo- nervous or psycho-organic type, that is, they are functions in which the material organism intimately cooperates; brute ani- mals give no indication of having so much as a single function, which proceeds from the soul alone and which is not communi- cated to the organism. Hence the bestial soul is "totally im- mersed" in matter; as regards both operation and existence, it is "intrinsically dependent" upon its material complement, the organism. It never operates save in conjunction with the lat- ter, and its sole reason for existence is adequately summed up in saying that it exists, not for its own sake, but merely to vivify and sensitize the organism. Consequently, the brute soul, though inextended and incorporeal, belongs, not to the spiritual, but to the material, order of things. Is the human soul equally material in nature, or does it belong to the spiritual category of being? The state of the question has long since been formulated for us by Aristotle: THE ORIGIN OF THE HUMAN SOUL 215 "A further diflBculty," he says, "arises as to whether all at- tributes 'of the soul are also shared by that which has the soul or whether any of them are peculiar to the soul itself: a problem which it is imperative, and yet by no means easy, to solve. It would appear that in most cases it neither acts nor is acted upon apart from the body: as, e.g., in anger, courage, desire, and sensation in general. Thought, if any- thing, would seem to be peculiar to the soul. Yet if thought is a sort of imagination, or something not independent of imagination, it will follow that not even thought is inde- pendent of the body. If, then, there be any functions or af- fections of the soul that are peculiar to it, it will be possible for the soul to be separated from the body: if, on the other hand, there is nothing peculiar to it, the soul will not be capable of separate existence." ("Peri Psyches," Bk. I, chap. I, 9.) We shall see that the human soul has certain operations which it discharges independently of the intrinsic coagency of the organism, e.g., abstract thought (not to be confounded with the concrete imagery of the imagination) and deliberate volition (to be distinguished from the urge of the sensual appetite). Hence, over and above the organic functions, which it discharges in conjunction with the material organism, the human soul has superorganic functions, of which it is itself, in its own right, the exclusive agent and recipient. In other words, it exists far its own sake and not merely to perfect the body. The Aristotelian argument for the spirituality of the human soul consists in the application of a self-evident principle or axiom to certain facts of internal experience. The axiom in question is the following: "The nature of an agent is revealed by its action"; or, to phrase it somewhat differently: "Every being operates after the same manner that it exists." The factual data, to which reference is made, are man's higher psychic functions, in which the soul alone is the active cause and receptive subject, namely: the rational or superorganic functions of thinking and willing. The argument may be for- 216 THE CASE AGAINST EVOLUTION mulated thus: Every agent exists after the same manner that it operates. But in rational cognition and volition the soul acts without the co-agency of the material organism. There- fore the human soul can exist without the co-existence of the material organism. But this is tantamount to saying that it is a spiritual reality irreducible to matter and incapable of derivation from matter. For we define that as spiritual, which exists, or is, at least, capable of existing, without matter. Con- sequently, the human soul is a supermaterial and immortal principle, which does not need the body to maintain itself in existence, and can, on that account, survive the death and dis- solution of its material complement, the organism. Such a reality, as we have seen, cannot be a product of evolution, but can only come into existence by way of creation. The axiom, that activity is the expression or manifestation of the entity which underlies it, needs but little elucidation. In the genesis of human knowledge, the dynamic is prior to both -the static and the entitive. We deduce the nature of the cause from the changes or effects that it produces. Action, in short, is the primary datum upon which our knowledge of being rests. It is the spectrum of solar light emitted by them, which enables us to determine the nature of the chemical elements present in the distant Sun. It is the reaction of an unknown compound with a test reagent that furnishes the chemist with a clue to its composition and structure. It is the special type of tissue degeneration caused by the specific toxin engendered by an invisible disease germ that enables the pathologists to identify the latter, etc., etc. So much for the axiom. Regarding the psychological facts, a more lengthy ex- position is required. To begin with, there is prima facie evi- dence against the contention that the higher psychic functions in man are independent of the organism. Injury and degenera- tion of the cerebral cortex result (very often, at least) in insanity and idiocy. Reason, therefore, is in some way de- pendent upon the organism. Babies, too, are incapable of rational thought until such a time as the nervous system is THE ORIGIN OF THE HUMAN SOUL 217 fully developed. Obviously, then, rational functions cannot be spiritual, inasmuch as they are not independent of the organism. This time-honored objection of materialists is based on a misapprehension. It falsely assumes that spirituality ex- cludes every kind of dependence upon a material organism, and that our assertion of the soul's independence of matter is an unqualified assertion. This, however, is far from being the case. It is only intrinsic (subjective), and not extrinsic (objective), independence of the organism which is here af- firmed. An analogy from the sense of sight will serve to make clear the meaning of this distinction. In the act of seeing a tree, for example, our sight is dependent upon a twofold cor- poreal element, namely, the eye and the tree. It is dependent upon the eye as upon a corporeal element intrinsic to the visual sense, the eye being a constituent part of the agent and sub- ject of vision; for it is not the soul alone which sees, but rather the soul-informed retina and neurons of the psycho- organic composite. The eye enters as an essential ingredient into the intimate constitution of the visual sense. It is a constituent part of the specific cause of vision, and it can therefore be said with perfect propriety that the eye sees. Such dependence upon a material element is called intrinsic or subjective dependence, and is utterly incompatible with spirituality on the part of that which is thus dependent. But the dependence of sight upon an external corporeal factor, like a tree or any other visible object, is of quite a different nature. Here the corporeal element is outside of the seeing subject and does not enter as an ingredient into the compo- sition of the principal and specific agent of vision. True the tree, which is seen, is coinstrumental as a provoking stimulus and an objective exemplar, but its concurrence is of an ex- trinsic nature, not to be confounded with the intrinsic co- agency of the eye in the act of vision. Hence, in no sense whatever can the tree be said to see; for the tree is merely m object, not the principal and specific cause, of vision. 218 THE CASE AGAINST EVOLUTION When the dependence of an agent upon a corporeal element is of this sort, it is termed extrinsic or objective dependence. Such dependence upon a material element is perfectly com- patible with spdrituality, which does, indeed, exclude all ma- teriality from the specific agent and subject of a psychic act, but does not necessarily exclude materiality from the object contemplated in such an act. Hence the fact that the thinking soul must abstract its rational concepts from the concrete imagery of a cerebral sense, like the imagination, in no wise detracts from its spirituality, because the dependence of ab- stract thought upon such imagery is objective or extrinsic, and not subjective or intrinsic. Psychologists of the sensationalist school have striven to obscure the fundamental distinction which exists between ra- tional thought and the concomitant cerebral imagery. It is, however, far too manifest to escape attention, as the healthy reaction of the modern school of Wlirzburg indicates. "It cost me great resolution," says Dr. F. E. Schultze, a member of this school, "to say, that, on the basis of immediate ex- periment, appearances and sensible apprehensions are not the only things that can be experienced. But finally I had to resign myself to my fate." ("Beitrag zur Psychologie des Zeitbewusstseins," p. 277.) But thought is not only distinct from imagery, often there is marked contrast between the two, both as regards sub- jective, and objective, characters. Thus our thought may be perfectly clear, precise, and pertinent, while the accompany- ing imagery is obscure, fragmentary, and irrelevant. "What enters into consciousness so fragmentarily, so sporadically, so very accidentally as our mental images," exclaims Karl Biihler (also of Wlirzburg), "can not be looked upon as the well-knitted, continuous content of our thinking." {Archiv. fur die ges. Psychol, 9, 1907, p. 317.) The same contrast exists with respect to their objective characters. Imagination represents by means of one and the same image what reason represents by means of two distinct concepts, e.g. an oasis THE ORIGIN OF THE HUMAN SOUL 219 and a mirage; and, vice versa, reason represents under the single general concept of a rose objects that imagination is forced to represent by means of two distinct images, e.g., a yellow, and a white rose. Imagery depicts only the super- ficial or exterior properties of an object, whereas thought penetrates beneath the phenomenal surface to interior prop- erties and supersensible relationships. The sensory percept apprehends the existence of a fact, while the rational concept analyzes its nature. Hence sense-perception is concerned with the reality of existence, while thought is concerned with the reality of essence. Certain American psychologists employ the term imageless thought to designate abstract concepts. The expression is liable to be misunderstood. It should not be construed as excluding all concomitance and concurrence of sensible im- agery, in relation to the process of thought. What is really meant is that sensible appearances do not make up the sum- total of our internal experiences, but that we are also aware of mental acts and states which are not reducible to imagery. In other words, we experience thought; and thought and im- agery, though concomitant, are not commensurable. The clar- ity and coherence of thought does not depend on the clarity or germaneness of the accompanying imagery, nor is it ever adequately translatable into terms of that imagery. Thus the universal triangle of geometry, which is not right, nor oblique, nor isosceles, neither scalene nor equilateral, neither large nor small, neither here nor there, neither now nor then, is not vis- ualizable in terms of concrete imagery, although we are clearly conscious of its significance in geometrical demonstrations. Imagery differs according to the person, one man being a visualist, another an audist, another a tactualist, another a motor-verbalist, etc. But thought is the same in all, and consequently it is thought, and not imagery, which we convey by means of speech. Helen Keller, whose imagery is mainly motor and tactile, can exchange views with an audist or vis- ualist on the subject of geometry, even though the amount 220 THE CASE AGAINST EVOLUTION of imagery which she has in common with such persons is negligible. ''Eine Bedeutung," says Biihler, "kann man uberhaupt nicht vorstellen, sondem nur wissen" and Binet, in the last sentence of his "L'Etude experimentale de I'intel- ligence," formulates the following conclusion: "Finally — and this is the main fact, fruitful in consequences for the phi- losophers — ^the entire logic of thought escapes our imagery." Nevertheless, thought does not originate in the total ab- sence of imagery, but requires a minimal substrate of sensible images, upon which it is objectively, if not subjectively, de- pendent. The nature of this objective dependence is explained by the Scholastic theory concerning the origin of concepts. According to this theory, the genesis of our general and ab- stract knowledge is as follows: (1) We begin with sense- perception, say of boats differing in shape, size, color, material, location, etc. (2) Imagination and sense-memory retain the composite and concrete imagery synthesized or integrated from the impressions of the separate external senses and representing the boats in all their factual particularity, individuality, and materiality, as existent here and now, or there and then, as constructed of such and such material (e.g., of wood, or steel, or iron, or con- crete), as having determinate sizes, shapes, and tonnages, as painted white, or gray, or green, as propelled by oar, or sail, or turbine, etc. (3) Then the active intellect exerts its abstractive influence upon this concrete imagery, accen- tuating the essential features which are common to all, and suppressing the individuating features which are peculiar to this or that boat, so that the essence of a boat may appear to the cognitive intellect without its concomitant individua- tion — ^the essence of a boat being, in this way, isolated from the peculiarities thereof and its various qualities from their subject (representatively, of course, and not physically). (4) The imagery thus predisposed, being no longer immersed in matter, but dematerialized by the dispositive action of the active intellect, becomes comstrumental with the latter in THE ORIGIN OF THE HUMAN SOUL 221 producing a determination in the cognitive intellect. (5) Upon receiving this determination, the cognitive intellect, which has hitherto been, as it were, a blank tablet with noth- ing written upon it, reacts to express the essence or nature of a boat by means of a spiritual representation or concept — the abstractive act of the active intellect is dispositive^ inasmuch as it presents what is common to all the boats perceived without their differentiating peculiarities; the ab- stractive act of the cognitive intellect, however, is cognitive, inasmuch as it considers the essence of a boat without considering its individuation. Such is the abstractive process by which our general and abstract concepts are formed. From a comparison of two concepts of this sort the process of judg- ment arises, and from the comparison of two concepts with a third arises the process of mediate inference or reasoning. Volition, too, is consequent upon conception, and hence an act of the will (our rational appetite), such as the desire of sailing in a boat, entails the preexistence of some conceptual knowledge of the nature of a boat. Volition, therefore, pre- supposes thought, and thought presupposes imagination, which supplies the sensible imagery that undergoes the aforesaid process of analysis or abstraction. Such imagery, however, is a function of the cerebral cortex, and, for this reason, the normal exercise of the imagination presupposes the cerebral cortex in a normal physiological condition; and anything that disturbs this normal condition of the cortex will di- rectly disturb the imagery of the imagination, and therefore indirectly impede the normal exercise of conceptual thought, which is abstracted from such imagery. Hence it is clear that the activity of both the intellect and the will is ob- jectively dependent upon the organic activity of the imagina- tion, and, in consequence, indirectly dependent upon the physiological condition of the cerebral cortex, which is the organ of the imagination. Since, however, this dependence is objective rather than subjective, it does not, as we have seen, conflict with the spirituality of rational thought. 222 THE CASE AGAINST EVOLUTION The nature of conceptual thought is such as to exclude the participation of matter as a constituent of its specific agent and receptive subject. The objects of a cerebral sense like the imagination are endowed with extension, color, shape, volume, mass, temperature, and other physical properties, in virtue of which they can set up vibrations in an extended medium or modify an extended organ by immediate physical contact. But, while imagination makes us conscious of ob- jects capable of stimulating extended material organs, the objects, of which we are conscious in abstract thinking, are divested of all the sensible properties, extension, and spe- cific energies, which would enable them to modify a material neuron, or produce a physical impression upon a material receptor of any kind whatever. Between an extended ma- terial receptor, like a sense-organ or a cerebral neuron, and the nondimensional, dematerialized object or content of an ab- stract thought, like science, heroism, or morality, there is no conceivable proportion. How can a material organ be af- fected by what is supersensible, unextended, imponderable, invisible, intangible, and uncircumscribed by the limitations of space and time? Extended receptors are necessary for picking up the vibrations of a tridimensional medium (like air or ether), and they are, likewise, essential for the recep- tion of impressions produced by surface-contact with an ex- terior corporeal mass. In short, sensory neurons are needed to receive and transmit inward the quantitative and measur- able excitations of the material stimuli of the external world, and central neurons are required as tablets upon which these incoming excitations may imprint extended neurograms, that are proportionate in intensity and extensity to the external stimulus apprehended, and that underlie and determine the concrete imagery (of which they are the physical basis). But when it comes to perceiving and representing the meaning of duty, truth, error, cause, effect, psychology, means, end, entity, logarithms, etc., our mind can derive no benefit from the cooperation of a material organ. In such thinking we THE ORIGIN OF THE HUMAN SOUL 223 are conscious of that which could not make an impression nor leave a record upon material receptors like neurons. To employ a material organ for the purpose of perceiving ab- stract essences and qualities would be as futile and pointless as an attempt to stop a nondimensional, unextended, intan- gible baseball with a catcher's glove. Hence the services of material centers and receptors may be dispensed with, so far as rational thought is concerned. Rational thought cannot utilize the intrinsic coagency of the organism, and it is therefore a superorganic or spiritual function. That conceptual thought is in no wise communicated to the organism, but subjected in the spiritual soul alone, is likewise apparent from the data furnished by introspection. The conceiving mind apprehends even material objects ac- cording to an abstract or spiritualized mode of representation. In other words, in conceiving material objects we expurgate them of their materiality and material conditions, endowing them with a dematerialized mode of mental existence which they could never have, if subjected in their own physical matter, or in the organized matter of the cerebral cortex. Thus, in forming our concept of a material object like a boat, we spiritualize the boat by separating (representatively, of course, and not physically) its nature or essence from the determinate matter {e.g., wood, or steel) of which it is made, and by divesting it of the material and concrete conditions which define not only its physical existence outside of us, but also its imaginal existence within us as a concrete image in our imagination. In other words, we isolate the type or form of a given object from its material substrate and lib- erate it from the limiting material and concrete individua- tion, which confine it to a single material subject and localize it definitely in space and time. Now, it is axiomatic that whatever is received is received according to the nature of the receiver. Water, for example, assumes the form of the receptacle into which it is poured, and a picture painted upon canvas is necessarily extended according to the extension of 224 THE CASE AGAINST EVOLUTION the canvas. If, therefore, our intellect endows even the ma- terial objects, which it perceives, with a dematerialized or spiritualized mode of representation, it follows that the in- tellect itself is a spiritual power and not an organic sense immersed in concretifying and individualizing matter. Cer- tainly, this ideal or spiritualized mode of existence does not emanate from the material object without nor yet from its vicarious material image in our organic imagination (which, in point of fact, is absolutely impotent to imagine anything ex- cept concrete, singular things in all their determinate in- dividuation and quantification). Thought, then, with its ab- stract mode of presentation, cannot, like imagery, be sub- jected in the animated or soul-informed cortex, but must have the spiritual mind alone as its receptive subject. Our abstract or dematerialized mode of conceiving material objects is a subjective character of thought, proceeding from, and mani- festing, the spirituality of the human mind, which represents even material objects in a manner that accords with its own spiritual nature. But it is not only in the process of abstraction, but also in that of reflection, that rational thought manifests its super- organic or spiritual character. The human mind knows that it knows and understands that it understands, thinks of its own thoughts and of itself as the agent and subject of its thinking. It is conscious of its own conscious acts, that is to say, it reflects upon itself and its own acts, becoming an object to itself. The thinking ego becomes an object of observation on the part of the thinking ego, which acquires self- knowledge by this process of reflective thought. In intro- spection, that which observes is identical with that which is observed. Now such a capacity of self-observation cannot reside in matter, cannot be spatially commensurate with a material organ nor inseparably attached thereto. It is pos- sible only to an immaterial or spiritual principle, devoid of mass and extension, and not subject to the law of the im- THE ORIGIN OF THE HUMAN SOUL 225 penetrability of matter. In virtue of the law of impenetra- bility, no two material particles, no two bodies, no two in- tegral parts of the same body, can occupy one and the same place. One part of a body can, indeed, act on another part extrinsic to itself; but one and the same part or particle cannot act upon itself. To become at once observed and observer, a material organ would have to split itself in two, so that the part watched could be distinct from, and spatially external to, the part watching. The power of perfect reflection, therefore, must reside in the spiritual soul, and cannot be bound to, and coextensive with, a material organ. Only in this supposition can there be a return of the subject upon and into itself, only in this supposition can there be that identification of observed and observer implied by the process of reflection. H. Griinder, in his "Psychology without a Soul," gives a graphic reductio ad absurdum of the contrary as- sumption: "A fairy tale," he says, "tells of a knight who was beheaded by his victorious foe. But, strange to relate, the vanquished knight rose to his feet, seized his severed head and bore it off, as in triumph. The most remarkable part, how- ever, of the story is that with a last effort of gallantry he took his own head, and — kissed its brow. The climax of this fairy tale is no more absurd than the assumption that a ma- terial organ can know itself and philosophize on itself. Only if we admit with the scholastics a simple soul intrinsically inde- pendent of any bodily organism, can we explain the possibility of perfect psychological reflexion." {Cf. pp. 193, 194.) For the rest the impossibility of introspection on the part of a material organ is so evident that the materialists them- selves freely concede it, and being unwilling to admit the spirituality of the human intellect, they are forced to resort to the disingenuous expedient of denying the fact of reflection on the part of the human mind. "It is obvious," says Auguste Comte, "that by an invincible necessity the human mind can observe directly all phenomena except its own. We 226 THE CASE AGAINST EVOLUTION understand that a man can observe himself as a moral agent, because in that case he can watch himself under the action of the passions which animate him, precisely because the organs that are the seat of those passions are distinct from those that are destined for the functions of observation. . . . But it is manifestly impossible to observe intellectual phe- nomena whilst they are being produced. The individual think- ing cannot divide himself in two, so that one half may think and the other watch the process. Since the organ observing and the one to be observed are identical, there can be no self-observation." ("Cours de philosophie posntive," liete leQon.) But an argument is of no avail against a fact, and, as a matter of fact, we do reflect. It is by introspection or reflective thought that we discriminate between our present and our past thoughts, and become conscious of our own con- sciousness. Our intellect even reflects upon its own act of reflection, and so on indefinitely, so that, unless we are pre- pared to accept the absurd alternative of an infinite series of thinkers, we have no choice but to identify the subject know- ing with the subject known. That our intellect is conscious of its own operations and attentive to its own thoughts, is an evident fact of internal experience, and it is preposterous to tilt against facts by means of syllogisms. When Zeno con- cocted his aprioristic "proof" of the impossibility of trans- latory movement, his sophism was refuted by the simple process of walking — solvitur ambulando. In like manner, the Comtean sophism concerning the impossibility of reflec- tion is refuted by the simple act of mental reflection — solvitur reflectendo. For the rest, we readily concede Comte's con- tention that an organ is incapable of reflection or self-obser- vation, but we deny his tacit assumption that our cognitive powers are all of the organic type. Our intellect, which attends to its own phenomena, thinks of its own thought and reasons upon its own reasoning, cannot be bound to, or co- extensive with, a material organ, but must be free from any corporeal organ and rooted in a spiritual principle. In a THE ORIGIN OF THE HUMAN SOUL 227 word, reflective thought is a superorganic function expressing the spiritual nature of the human mind. Another proof of the superorganic nature of the human intellect as compared with sentiency, both exterior and in- terior, is one adduced by Aristotle himself: "But that the im- passivity of the sense," he says, "is different from that of intellect is clear if we look at the sense organs and at sense. The sense loses its power to perceive, if the sensible object has been too intense; thus it cannot hear sound after very loud noises, and after too powerful colors or odors it can neither see nor smell. But the intellect, when it has been thinking on an object of intense thought, is not less, but even more, able to think of inferior objects. For sense-perception is not inde- pendent of the body, whereas the intellect is." ("Peri Psyches," Bk. Ill, Ch. iv, 5.) This temporary incapacitation of the senses consequent upon powerful stimulation is a common experience embalmed in such popular expressions as "a deafening noise," "a blinding flash," "a dazzling light," "a numbing pain," etc. Weber's law of the differential threshold tells us that the intensity of sensation does not increase in the same proportion as that of the stimulus. On the contrary, the more intense the previous stimulus has been, the greater must be the increment added to the subsequent stimulus before it can produce a perceptible increase in the intensity of sensation. In short, stimulation of the senses temporarily decreases their sensitivity with ref- erence to supervening stimuli. The reason for this momentary loss of the power to react normally is evidently due to the organic nature of the senses. Their activity entails a definite and rigidly proportionate process of destructive metabolism in their bodily substrate, the organism. In other words, the exer- cise of sense-perception involves a commensurate process of decomposition in the neural tissue, which must afterwards be compensated by a corresponding assimilation of nutrient ma- terial, before the sense can again react with its pristine vigor. This process of recuperation requires time and temporarily 228 THE CASE AGAINST EVOLUTION inhibits the reactive power of the sense in question, the dura- tion of this repair work being determined by the amount of neural decomposition caused by the reaction of the sense to the previous stimulus. When, therefore, a weaker stimulus supervenes in immediate succession to a stronger one, the sense is incapable of perceiving it. All organic activity, in short, such as sense-perception and imagination, is rigidly regulated by the metabolic law of waste and repair. With the intellect, however, the case is quite different. The intellect is neither debilitated nor stupefied by the discovery of truths that are exceptionally profound, or unusually abstruse, or strikingly evident; nor is it temporarily incapacitated thereby from understanding simpler, easier, or less evident truths. On the contrary, the more comprehensive, the more penetrating, the more perspicuous, the more sublime our intel- lectual vision is, so much the more is our intellect invigorated and enthused in its pursuit of truth, and its knowledge of the highest truths renders it not less, but more, apt for the under- standing of simple and ordinary truths. Obviously, then, the intellect is not bound to a corruptible organ like the senses, but has for its subject a spiritual principle that is intrinsically independent of the organism. In opposition to this contention, it may be urged that a pro- longed exercise of intellectual activity results in the condition commonly known as brain-fag. But this fatigue of the brain is not, as a matter of fact, the direct effect of intellectual activity; rather it is the direct effect of the activity of the imagination, and only indirectly the effect of intellectual thought. The intellect, as we have seen, requires a constant flow of associated and aptly coordinated imagery as the sub- strate of its contemplation. Now, the imagination, which supplies this imagery, is a cerebral sense, whose activity is directly proportionate to, and commensurate with, the meta- bolic processes at work in the cortical cells. Its exercise is directly dependent upon the energy released by the decompo- sition of the cerebral substance. Prolonged activity of the THE ORIGIN OF THE HUMAN SOUL 229 imagination, therefore, involves the destruction of a consider- able amount of the cortical substance, and results in temporary incapacitation or paralysis of the imagination, which must then be compensated by a process of repair in the cortical neurons, before the imagination can resume its normal mode of functioning. Brain-fag, then, is due to the activity of the imagination rather than that of the intellect. That such is the case appears from the fact that after the initial exertion, which results from the imagination being forced to assemble an appropriate and systematized display of illustrative imagery as subject-matter for the contemplation of the intel- lect, the latter is henceforth enabled to proceed with ease along the path of a given science, its further progress being smooth and unhampered. Once the preliminary work imposed upon the imagination is finished, the sense of effort ceases and intel- lectual investigation and study may subsequently reach the highest degrees of concentration and intensity, without involv- ing corresponding degrees of fatigue or depression on the part of the cerebral imagination, just as, conversely speaking, the activity of the cerebral imagination may reach degrees of in- tensity extreme enough to induce brain-fag in psychic opera- tions wherein the concomitant intellectual activity is reduced to a minimum, e.g., in the task of memorizing a poem, or reci- tation. Here, in the all but complete absence of intellectual activity, the same fatigue results as that induced by a pro- longed period of analytic study or investigation, in which imaginative activity and rational thinking are concomitant. The point to be noted, in this latter case, is that the intellect does not show the same dependence upon the physiological vicissitudes as the imagination. The imagery of our imagina- tion, being rigidly correlated with the metabolic processes of waste and repair at work in the cerebral cortex, manifests correspondingly variable degrees of intensity and integrity, but the intensity of thought is not dependent upon this alterna- tion of excitation and inhibition in the cortex. Hence, while the concomitant imagery is fitful, sporadic, and fragmentary, 230 THE CASE AGAINST EVOLUTION intellectual thought itself is steady, lucid, and continuous. The intensity of thought does not vary with the fluctuations of neural metabolism, and may reach a maximum without involving corresponding fatigue in the brain. The brain-fag, therefore, which results from study does not correspond to the height of our intellectual vision, but is due to the intensity of the concomitant imaginative process. The intellect, therefore, is not subject to the metabolic laws which rigidly regulate organic functions like sense-p€rception and imagination. Man's capacity for logical thought is fre- quently unaffected by the decline of the organism which sets in after maturity. All organic functions, however, such as sight, hearing, sense-memory, are impaired in exact proportion to the deterioration of the organism, which is the inevitable sequel of old age. The intellectual powers, on the contrary, remain unimpaired, so long as the cortex is sound enough to furnish the required minimum of imagery, upon which intel- lectual activity is objectively dependent. There are, in fact, many cases on record where men have remained perfectly sane and rational, despite the fact that notable portions of the cerebral cortex had been destroyed by accident or disease {e.g., tumors). Intellectual thought, therefore, is a super- organic function, having its source in a spiritual principle and not in a corruptible organ. Such is the spiritualism of Aristotle. That this conception differs profoundly from the ultra-spiritualism of Descartes, it is scarcely necessary to remark. The position assumed by the latter was always untenable, but it is now, more than ever, indefensible in the face of that overwhelming avalanche of facts whereby modern physiological psychology demonstrates the close interdependence and correlation existent between psychic and organic states. Such facts are exploited by ma- terialists as arguments against spiritualism, though it is evi- dent that they have force only against Cartesian spiritualism, and are bereft of all relevance with respect to Aristotelian spiritualism, which they leave utterly intact and unscathed. THE ORIGIN OF THE HUMAN SOUL 231 In the latter system, sense-perception, imagination, and emo- tion are acknowledged to be directly dependent on the organ- ism. Again, spiritual functions like thinking and willing are regarded as objectively or extrinsically dependent upon the imagination, which, in turn, is directly dependent on a material organ, namely: the brain. Hence even the rational operations of the mind are indirectly dependent upon the cerebral cortex. The spiritualism of Aristotle, therefore, by reason of its doc- trine concerning the direct dependence of the lower, and the indirect dependence of the higher, psychic functions upon the material organism, is able to absorb into its own system all the supposedly hostile facts amassed by Materialism, thereby rendering them futile and inconsequential as arguments against the spirituality of the human soul. In confronting this philosophy, the materialistic scientist finds himself disarmed and impotent, and it is not to be wondered at, that, after indulging in certain abusive epithets and a few cant phrases, such as "metaphysics" or "medieval" (invaluable words!), he prudently retires from the lists without venturing to so much as break a lance in defense of his favorite dogma, that nothing is spiritual, because all is matter. In this predica- ment, the Cartesian caricature proves a boon to the material- ist, as furnishing him with the adversary he prefers, a man of straw, and enabling him to demonstrate his paltry tin- sword prowess. Of a truth, Descartes performed an inestima- ble service for these modern "assassins of the soul," when he relieved them of the necessity of crossing swords with the hylomorphic dualism of Aristotle by the substitution of a far less formidable antagonist, namely, the psychophysical dualism of mind and matter. The proofs advanced, in the previous pages, for the spiritu- ality of the human soul are based upon the superorganic function of rational thought. A parallel series of arguments can be drawn from the superorganic function of rational volition. The cognitive intellect has for its necessary sequel the appetitive will, which may be defined as spiritual tendency 232 THE CASE AGAINST EVOLUTION inclining us toward that which the intellect apprehends as good. The objects of such volition are frequently abstract and immaterial ideals transcendent to the sphere of concrete and material goods, e.g., virtue, glory, religion, etc. The will of man, moreover, is free, in the sense that it can choose among various motives, and is not compelled to follow the line of least resistance, as is the electric current when passing through a shunt of steel and copper wire. Like the self-knowing intel- lect, the self-determining will is capable of reflective action, that is, it can will to will. Having its own actions within its own control, it is itself the principal cause of its own decisions, and thus becomes responsible for its conduct, wherever its choice has been conscious and deliberate. External actions, which escape the control of the will, and even internal actions of the will itself, which are indeliberate, are not free and do not entail responsibility. Our courts of law and our whole legal system rests on the recognition of man's full responsi- bility for his deliberate voluntary acts. The distinction between premeditated murder, which is punished, and unpre- meditated homicide, which is not, is purely moral, and not physical, depending for its validity upon the fact of human freedom. It is this exemption from physical deter- minism, that makes man a moral agent, subject to duties, amenable to moral suasion, and capable of merit or demerit. Finally, the will of man is insatiable, invincible, and inex- haustible. The aspirations of the will are boundless, whereas our animal appetites are easily cloyed by gratification. There is no freezing point for human courage. The animal or sensual appetites wear out and decline with old age, but virtue and will-power do not necessarily diminish with the gradual de- terioration of the material organism. Willing, therefore, is a superorganic or spiritual function. Activity which is bound to a material organ cannot tend towards supersensible ideals, cannot escape physical determinism, cannot achieve the reflec- tive feat of spurring itself to action, cannot avoid exhaustion, cannot elude rigid regulation by the laws of organic metab- THE ORIGIN OF THE HUMAN SOUL 233 olism. For this reason, the brute, whose psychic functions are of the organic type exclusively, is destitute of freedom, moral- ity, and responsibility. Deliberate volition, therefore, like conceptual thought, has its source and subject in man's spir- itual soul, and is not a function of the material organism.^ *To develop the argument drawn from rational volition for the spirituality of the human soul would carry us too far afield. Those who wish to pursue the subject further may consult Chapter VIII of Griinder's monograph entitled "Psychology without a Soul," also his monograph on "Free Will." G. H. Parker of Harvard, though admitting the fact of human free- dom, tries to explain it away in terms of materialism. The following is the description which he gives of his theory: "It is a materialist view which, however, recognizes in certain types of organized matter a degree of free action consistent with human behavior and the resultant responsibility." (Science, June 13, 1924, p. 520.) Freedom, in other words, "emerges" from matter having a peculiar "type of organization." This view must be interpreted in the light of the philosophy of "Emergent Evolution," which Parker holds in common with C. Lloyd Morgan and R. W. Sellars. The philosophy in question recognizes in nature an ascending scale of more and more complexly organized units, starting with protons and electrons, at the bottom, and culminating in the human organism, at the top. At each higher level of this cosmic scale we find higher units formed by coalescence of the simpler units of a lower level. These higher units, however, are something more than a mere summation of the lower units; for, in addition to additive properties that can be predicted from a knowledge of the components, they exhibit genuinely new properties which, not being mere sums of the properties of the component units, are unpredictable on that basis. Given, for example, the weight of two volumes of hydrogen and one volume of oxygen, we could predict an additive property such as the weight of the compound, i.e. the water, formed by their combination. Other properties, of the compound, however, such as liquidity, are not foreshadowed by the properties of the component gases. Similarly, the weight of carbon disulphid (CS2) is an additive function of the com- bining weights of sulphur and carbon, but the other properties of this mobile liquid are not predictable on the basis of the properties of sul- phur and carbon. Hence two kinds of properties are distinguished: (1) additive (quantitative) properties called resultants, which are predict- able; (2) specificative (qualitative) properties called emergents, which are unprecedented and unpredictable. Freedom and intelligence, ac- cordingly, are pronounced to be emergents of matter organized to that degree of complexity which we find in man. This dualism of resultance and emergence is merely a new verbal vesture for the hylomorphic dualism of Aristotle. The additive proper- 234 THE CASE AGAINST EVOLUTION Two additional facts may be cited as bringing into strong relief the basic contrast existing between the higher or rational, and the lower or animal psychosis in man. The first is the occurrence of irreconcilable opposition or conflict. The imag- ination, for example, antagonizes the intellect by visualizing as an extended speck of chalk or charcoal the mathematical point, which the intellect conceives as destitute of extension and every other property except position. Similarly, the effort of our rational will to be faithful to duty and to uphold ties (resultants) are based on matter, which is the principle of continu- ity. The specificative (constituitive or qualitative) properties called emergents are rooted in entelechy (form), which is the principle of novelty. In fact, entelechy (form) itself is an emergent of matter just as the specificative properties are emergents of matter, with the sole difference that entelechy is the primary emergent of matter, whereas the specificative or qualitative properties are secondary emergents. For in Aristotelian philosophy, entelechy is not, as it is in Neo-vitalism, *'an alien principle inserted into matter" abruptly and capriciously "at the level of life," but a primary emergent and constituent of matter both living and non-living. In fine, entelechy is an emergent of matter in all the units of nature from the simplest atom to the most complex plant or animal organism. The only entelechy, which is not an emergent, but an insert into matter, is the spiritual human soul. Neither the human soul nor the superorganic functions rooted in it, namely, abstrac- tion, reflection, and election, are emergents. Here we have novelty without continuity, and therefore not emergence (eduction), but irir- sertion (infusion). In his "Emergent Evolution," 1923, Lloyd Morgan lays it down as axiomatic that emergence involves continuity — "There may often be resultants," he says, "without emergence; but there are no emergents that do not involve resultant effects also. Resultants give quantitative continuity which underlies new constitutive steps in emergence." (Op. cit., p. 5.) Now our proofs for human spirituality consist precisely in the complete exclusion of qiiantitative continuity between organic func- tions (e.g. sensation) and superorganic functions (e.g. conceptual thought and free volition). Hence, by the very axiom which Morgan himself formulates, the human soul and its superorganic functions are excluded from the category of material emergents. If there can be no emergence without quantitative continuity, then the human soul is not an emergent Jrom, but an insert into, matter. Free choice, too, it is need- less to say, is not an emergent of matter, but an expression of the super- material nature of the human soul. So much for the new-old dualism of emergence and resultance. THE ORIGIN OF THE HUMAN SOUL 235 ideals is antagonized by the sensual impulses of the animal appetite, which seek immediate gratification at the expense of remote considerations that are higher. Such antagonism is incompatible with any identification of the warring factors, that is, of our rational, with our sentient, functions; for, wher- ever opposition is in evidence, there a fortiori a real distinction must be recognized. The understanding and the will, there- fore, differ radically from sense and sensual appetite. The second significant fact is the domination exerted by reason and will over the cognitive and appetitive functions of the organic or sentient order. Our intellect criticizes, evaluates and corrects the data of sense-perception, it discriminates be- tween objective percepts and illusions and hallucinations, it distinguishes dreams from realities, it associates and dissoci- ates imagery for purposes of comparison, contrast, illustration, or analysis. Moreover, it not only shows its superiority to sense by supervising, revising, and appraising the data of sentient experience, but it manifests its discontent at the inac- curacy and limitation of sense by the invention and use of instrumentation {e.g. ear trumpets, spectacles, microscopes, telescopes, spectroscopes, polariscopes, periscopes, etc.) to rem- edy the defects or increase the range of sense-perception, etc. This phenomenon is without parallel among brute animals, and is a patent manifestation of the superiority of human psy- chology. In like manner, the will demonstrates its preemi- nence over the organic or animal appetite, by exerting supreme control over the passions and impulses of our lower nature. In fact, it is able to bridle and repress the impulses of sensu- ality even in the immediate presence of sensible stimuli that would irresistibly determine the brute to a gratification of its animal lusts ; and it can force the struggling and reluctant flesh to undergo a crucifixion for supersensible motives that make no appeal to the beast. The understanding and the will, there- fore, are essentially superior to the organic psychosis that they control, namely, the sentient consciousness and sensual appetite, which we share in common with the brute, but which. 236 THE CASE AGAINST EVOLUTION in the latter, give no evidence whatever of rational or moral control. § 4. Darwinian Anthropomorphism The spiritual mind of man represents an eminence to which evolving matter can never attain. This, then, is the hill that must needs be laid low, if the path of Darwinian materialism is to be a smooth one. There is, therefore, nothing very sur- prising in the fact that Darwin and his followers, from Huxley down to Robinson, have done all in their power to obscure and belittle the psychological differences between man and the brute. The objective of their strategy is twofold, namely, the brutalization of man and its converse, the humanization of the brute. The ascent will be easier to imagine, if man can be depressed, and the brute raised, to levels that are not far apart. To this end, the Darwinian zealots have, on the one hand, spared no pains to minimize the superiority and dignity of human reason by the dissemination of sensistic association- ism, psychophysical parallelism, and various other forms of "psychology without a soul"; and they have striven, on the other hand, to exalt to the utmost the psychic powers of the brute by means of a crude and credulous anthropomorphism, which, for all its scientific pretensions, is quite indistinguish- able from the naivete of the author of "Black Beauty" ^ and the sentimentality of S. P. C. A. fanatics, vegetarians, anti- vivisectionists, etc. The first of these tendencies we have already discussed, the second remains to be considered. When it comes to anthropomorphizing the brute, Darwin has not been outdistanced by the most reckless of his disciples. Three entire chapters of the "Descent of Man" are filled with this "vulgar psychology" (as Wundt so aptly styles it). It is the sum and substance of the entire fabric of argumentation, which he erects in support of his thesis that "the difference in 'Title of a horse's autobiography by Anna Sewall, the horse's alter ego. THE ORIGIN OF THE HUMAN SOUL 237 mind between man and the higher animals is certainly one of degree and not of kind." (C/. op. cit., chs. III-V.) Haeckel, Huxley, and Clifford attained to equal proficiency in the sport. Subsequent philosophers parroted their bold metaphors and smart aphorisms,