Hae yycaivieiese oman eer pee fies ni iy ° @ Ty att ran ANew Pork ~— State College of Agriculture At Cornell Gniversitp — Bthaca, N. D. Library Be ‘wae Cornell University Library The original of this book is in the Cornell University Library. There are no known copyright restrictions in the United States on the use of the text. http://www.archive.org/details/cu31924003044660 CHARLES DARWIN AND THE ORIGIN OF SPECIES ADDRESSES, ETC., IN AMERICA AND ENGLAND IN THE YEAR OF THE TWO ANNIVERSARIES BY EDWARD BAGNALL POULTON, D.Sc., M.A. Hon. LL.D. Princeton, F.R.S., V-P.L.S., F.Z.S., F.G.S., F.E.S. HOPE PROFESSOR OF ZOOLOGY IN THE UNIVERSITY OF OXFORD FELLOW OF JESUS COLLEGE, OXFORD MEMB, HON. 800, ENT. BELG. ; S00, HON. REAL 800, ESPAN, HIST. NAT, CORRESP. MEMB. ACAD. SCI., NEW YORK, AND SOO. NAT. HIST. BOSTON AUTHOR OF ‘ESSAYS ON EVOLUTION’, ETC. PUBLISHED NOV. 24, 1909, BEING THE FIFTIETH ANNIVERSARY OF THE PUBLICATION OF ‘THE ORIGIN OF SPECIES’ LONGMANS, GREEN, AND CoO. 39 PATERNOSTER ROW, LONDON NEW YORK, BOMBAY, AND CALCUTTA 1909 ty TO ALFRED RUSSEL WALLACE WHO GAVE TO HIS BOOK ON NATURAL SELECTION THE TITLE ‘DARWINISM’, THIS COLLECTION OF ADDRESSES ON DARWIN AND THE ‘ORIGIN’ IS AFFECTIONATELY DEDICATED PREFACE Dvurine the fourteen months preceding the date on which this volume is issued I have devoted all available time to work connected with the three inspiring anniversaries of July 1, 1908, Feb. 12, 1909, and Nov. 24, 1909. With all diffidence I have chosen the date which closes this period of work, as the day of publication. It may help in some small degree to keep in remembrance the birthday of a mighty epoch in the history of thought. The first Section of this book attempts to give a brief account of the history which led up to and followed the publication of the theory of Natural Selection and the Origin of Species. Darwin’s sure scientific insight, and his views on evolution by mutation, briefly treated in this Section, receive further consideration in Appendices A and B. The confusion of thought threatened by the unintentional but most unfortunate mis- representation of de Vries’s term, ‘ fluctuating variability, is pointed out in a footnote and further considered in Appendix D. I have given at the end of this Appendix a very brief account of certain phases of thought, during the past vi PREFACE half century, on the variations forming the material out of which the steps of evolutionary progress have been supposed to be built. The influence of Darwin’s personality upon the intellectual revolution of the past fifty years is considered in the second Section. The wide- spread misunderstanding of the changes which Darwin describes in his own mind, and the consequent injustice to scientific men generally, and especially to Darwin himself, not only form the subject of argument and protest in this Section, but also occupy nearly all the brief third Section, part of the seventh, and the whole of Appendix C. The unfortunate misinterpretations referred to above require, for their complete and final refuta- tion, the collection from Darwin’s correspondence of a large number of passages bearing upon health. These, placed together, may convey to the hasty reader an entirely wrong impression of Darwin’s heroic spirit, and I therefore trust that the words on p. 216 will be remembered whenever such passages may be read. In the fourth Section the relationship of Darwin to the two ancient English Universities, and especially to his own University of Cambridge, is very briefly considered. The fifth Section is concerned with one of the first and still perhaps the most striking of the PREFACE vii interpretations that have sprung from the theory of Natural Selection. The subject, ‘the Value of Colour in the Struggle for Life,’ is treated histori- cally. Darwin’s own hypotheses and discoveries in this line, and his keen interest in the hypotheses and discoveries of others are especially considered here and also in part of the seventh Section. The sixth Section deals with Mimicry, the most arresting of all the uses which colour may subserve in the struggle for existence. It is maintained that this complicated subject is best approached by the study of North American examples, and attention is directed to the number of inspiring problems which await a thorough and systematic attack by American naturalists. Darwin’s hitherto unpublished letters to Mr. Roland Trimen, F.R.S., form the subject of the seventh Section. An interesting account of Mr. Trimen’s first meeting with the illustrious naturalist fifty years ago is also included. In addition to the eighteen letters in Section VII, four written by Darwin to other correspondents are published in this volume—one in Section I, two in Section V, and one in Section VI. I desire to thank my friends for generously lending me these twenty-two deeply interesting letters, and Mr. Francis Darwin for kindly permitting their publication. viii PREFACE The occasions on which the addresses here printed were delivered are described in an introductory note at the beginning of each Section. Three out of the seven Sections of this volume, viz. I, IV, and V, have already appeared ; four are now published for the first time. I have especial reasons for being grateful to my American friends for permission to reprint the address contained in the first Section. The Publi- cation Committee of the American Association for the Advancement of Science did me the honour of choosing the title of my address as the title of the complete work—Fifty Years of Darwinism,—containing the eleven centennial addresses, in honour of Charles Darwin, delivered on Jan. 1, 1909. The-publishers who owned the copyright were very doubtful about the success of the work—unnecessarily as it happened, for I understand that a second edition is already being prepared. In spite of considerations which seemed at the time to be weighty, both Com- mittee and Publishers at once granted me the most free and cordial permission to reprint the address in the present work. The Syndics of the Cambridge University Press generously allowed the publication, on Nov. 24, of Section V, which had appeared as Essay XV of Darwin and Modern Science only eight months PREFACE ix earlier, the Preface being dated March 20, 1909. I also desire to acknowledge the kind permission to publish Section IV from Darwin Celebration, Cambridge, June, 1909. Speeches delivered at the Banquet held on June 28rd, printed for private cir- culation by Sir George Darwin and Mr. Francis Darwin. In these later years the multitudes seem, for the moment at least, to recognize a prophet in every reed shaken with the wind. It would be interesting to know the number of forgotten works, of works soon to be forgotten, of works dead before they were born, which have been proclaimed as ‘the most important contribu- tion to biological thought since the appearance of the Origin of Species’. I would that the multitudes were not mere followers of the fleeting scientific fashions of a day, but that they were right in their intuitions: I would that Newtons and Darwins might arise in every generation. I cannot admit that the inability to see them on every side is merely the natural consequence of a cynical and pessimistic spirit. I am fully aware of the intellectual rigidity that is so prone to develop with the passing years; but to know the danger is in some measure to be armed against it. I have steadily endeavoured to keep my mind elastic and flexible; and, in my own special x PREFACE line of work, have again and again abandoned the most dearly loved hypothesis when a new interpretation was seen to be more consistent with an ever-growing store of facts. And I submit that it is even more difficult to keep an open mind in the pursuit of a special line of research than in the consideration of the broadest and most far-reaching problems which confront the human intellect. Although the splendidly thorough work of the present day must rightly compel the warmest admiration, there are valid reasons why we should direct a searching and critical gaze upon the pro- clamation of each enthusiastic specialist that the foundations of organic evolution are wholly sur- rounded by the boundaries of his own field of inquiry. Organic evolution, to be understood, must be studied not in the light of one special line of work, but of all. This was the great secret of Darwin’s unique power in dealing with it. He could see the subject from all sides. And an ample measure of Darwin’s strength was possessed by his great comrades of half acentury ago. How we long for a little of the sure insight and com- prehensive vision of Asa Gray as we read the address of his distinguished living representative, Professor J. M. Coulter, who considers that an adaptive response to environment is destructive of Natural Selection, and finds it hard to imagine PREFACE si how Darwinism can account for the valuable mechanical functions of lifeless structures. And even more arresting is the contrast between Darwin’s outlook on the world of life and that of the eminent Dutch botanist who raised fresh strains, or perhaps sorted over again old mixtures of Evening Primroses, and straightway said to his friends: ‘Go to, let us build us an exalted theory of evolution based on the conception of an inborn transforming force violently discharged at regular intervals by every species of times past, present, and to come.’ And the historic fate of the too-ambitious builders of Babel is already evident ; for, when Professor de Vries, Professor Bateson, and Mr. R. C. Punnett begin to talk of variability in its commonest form, their language is confounded, ‘that they may not understand one another's speech.’ And when we remember that the two last-named authorities are the recog- nized English exponents of the views of the first- named, it will be realized that the confusion which has resulted from the misunderstanding of the words ‘acquired character’ and the word ‘Mimicry’ is as nothing to the confusion worse confounded which is even now upon us. The misunderstanding of de Vries by his exponents does however help us to solve one mystery,—the 1 Fifty Years of Darwinism, New York (1909), 61-5. See also the Quarterly Review (July, 1909), 7. 2 See 49, and Appendix D, 258. xii PREFACE extraordinary and,—as many naturalists think,— the unwarrantable exaggeration of the importance of the Dutch botanist’s contributions to evolution. Omne ignotum pro magnifico. If de Vries had indeed proved, as his exponents assert, that the ‘individual differences’ in which Darwin saw the steps of evolutionary progress—the ‘individual differences’ whose behaviour in heredity is the life- work of Francis Galton—that these are in fact non- transmissible to offspring, then surely the great- ness of him who demonstrated such a discovery to the world might be justly measured by the depth of the error into which his predecessors had fallen. I need hardly say that de Vries makes no such claim, but, on the contrary, shows us again and again that hereditary transmission to offspring is essential to his conception of ‘fluctuating varia- bility ’. For de Vries’s laborious and original investiga- tions every one must feel the warmest admiration. He and his friend Professor Hubrecht have always been most anxious to emphasize their conclusion that the Mutationstheorie is Darwinian, and they are equally anxious to disown and dis- credit any attempts to use it as a weapon against Darwin. They have even fallen into the error of maintaining that Darwin anticipated de Vries in holding the main conclusion of the Mutationstheorie —the origin of species by the selection of large PREFACE xiii single variations.’ It is with great reluctance that Thave protested against the unduly important posi- tion which, as I believe, is assigned to de Vries’s work and conclusions in the history of evolution. The Darwinian of the present day holds an inter- mediate position between the followers of Buffon and Lamarck, and the Mutationists, with whom the Mendelians are somewhat unnecessarily allied. The disciple of the two first-named naturalists, in these days calling himself an oecologist, main- tains that organisms are the product of their environment : the Mutationist holds that organ- isms are subject to inborn transformation, and that environment selects the fittest from among a crowd of finished products. The Darwinian believes that the finished product or species is gradually built up by the environmental selection of minute increments, holding that, among inborn variations of all degrees of magnitude, the small and not the large become the steps by which evolution proceeds. He attempts to avoid, as Darwin did, on the one hand the error of as- cribing the species-forming forces wholly to a creative environment, and, on the other, the perhaps more dangerous error of ascribing them wholly to creative internal tendencies. ! Both professors of course admit that Darwin also believed in an evolution founded on the selection of ‘individual differences ’. xiv PREFACE The failure of the earlier attacks on the Origin has been referred to in many pages of this book ; but my chief object throughout has been to speak of Darwinism and of Darwin himself. Hence Mendelism, entirely unknown to the illustrious naturalist, is on this occasion barely mentioned.’ The conception of evolution by mutation, on the other hand, is shown to have been from the first entirely familiar to Darwin, and entirely rejected by him. In the Quarterly Review? for July, 1909, I have ‘endeavoured to set forth—necessarily with brevity—the chief results of those modern investigations which, after fifty years, are now believed to be charged with menace for the Darwin-Wallace hypothesis’; and I will con- clude by quoting the final words of the article: ‘The inspiration of these investigations has at- tracted a numerous band of enthusiastic and devoted labourers, who have achieved and are achieving results of the highest interest and im- portance. No one of these, it is here maintained, can be reasonably held to make good the claims of the modern opponent of natural selection and evolution as conceived by Darwin. The only fundamental changes in the doctrine given to us ' See however the close of Appendix D Attention is directed in Section VI to certain North American butterflies which appear to afford a peculiarly favourable opportunity of testing the working of Mendel’s law under natural conditions. ; ? ‘The Centenary of Darwin: Darwin and his Modern Critics,’ -38. PREFACE XV in 1858 and 1859 are those brought about by the researches and the thoughts of Weismann ; and these have given to the great theory which will ever be associated with the names of the two illustrious English naturalists a position far higher than that ever assigned to it by Darwin himself.’ EDWARD B. POULTON. OxFoRD, Nov. 24, 1909. CONTENTS I. Firry Years or Darwinism (Baltimore, Jan. 1, i. w. -. @ «a a & II. Tar Personauity of Cuartes Darwin (Balti- more, Jan. 1, 1909) III. Tuz Darwin Centenary at Oxrorp (Feb. 12, S03 s “So af « & iw & IV. Cuarites Darwin AnD THE UNIVERSITY OF CAmM- BRIDGE (Cambridge, June 23, 1909) . V. Tue Vauve or CoLour IN THE STRUGGLE FoR LIFE VI. Mimicry 1n tHe Burrerriies oF NortH AMERICA (Baltimore, Dec, 31, 1908) . ‘ ; . VII. Lerrers rrom Cuarites Darwin To RoLanp Trimen (1863-71) ; . : . . APPENDIX A. Cuar.tes Darwin anp THE Hypo- THESIS OF MuLTIPLE ORIGINS . ‘ APPENDIX B. Darwin ann Evouution sy Mv- TATION . , ‘ ‘ j ‘ i ‘ APPENDIX ©. Furruer Proor tuat ScrEenriric WorK WAS NECESSARY FOR Darwin. APPENDIX D. De Vrtss’s ‘ Fiucruations’ HERE- DITARY ACCORDING TO DE VRIES, NON-TRANS- MISSIBLE ACCORDING TO BatTESON AND Punnett INDEX . : PAGE 144 213 247 254 256 258 281 I FIFTY YEARS OF DARWINISM One of the centennial addresses in honour of Charles Darwin, read before the American Association for the Advancement of Science, Baltimore, Friday, January 1, 1909. Revised and extended. On this historic occasion it is of special interest to reflect for a few moments on the part played by the New World in the origin and growth of the great intellectual force which dominates the past half-century. The central doctrine of evolu- tion, quite apart from any explanation of it, was first forced upon Darwin’s mind by his South American observations during the voyage of the Beagle; and we may be sure that his experience in this same country, teeming with innumerable and varied forms of life, confirmed and deepened his convictions as to the importance of adaptation and thus prepared the way for Natural Selection. Wallace, too, at first travelled in South America, and only later in the parts of the Old World tropics which stand next to South America in richness. Asa Gray in the New World represents Sir Joseph Hooker in the Old, as regards the help given to Darwin before the appearance of B 2 FIFTY YEARS OF DARWINISM the Origin; and in strenuous and most efficient defence after its appearance, Chauncey Wright similarly represents Henry Fawcett. Fritz Miller not only actively defended Darwin, but continually assisted him by the most admirable and original observations carried out at his Brazilian home. Turning to those who in some important respects differed from Darwin, I do not think a finer example of chivalrous con- troversy can be found than that carried on between him and Hyatt. The immense growth of evolutionary teaching, in which John Fiske played so important a part, although associated with the name of Herbert Spencer, must not be neglected on an occasion devoted to the memory of Darwin. Outside the conflict which raged round the Origin, we find Dana the only naturalist who at first supported Darwin in his views on the persistence of ocean basins and continental areas, and Alexander Agassiz, for many years the principal defender of the Darwinian theory of coral islands and atolls. American Palaeontology, famed throughout the world, has exercised a profound influence on the growth and direction of evolutionary thought. The scale and perfection of its splendid fossil records have attracted the services of a large band of the most eminent and successful labourers, of whom I can only mention the leaders :—Leidy, Cope, Marsh, Osborn, and Scott, in the Verte- AMERICA AND EVOLUTION 3 brata; Hall, Hyatt, and Walcott in the Inverte- brata. The study of American Palaeontology was at first believed to support a Neo-Lamarckian view of evolution, but this, as well as the hypo- thesis of polyphyletic or multiple origins (see Appendix A, p. 247), was undermined by the teachings of Weismann. Difficulties for which the Lamarckian theory had been invoked were met by the hypothesis of Organic Selection, sug- gested by Baldwin and Osborn, and in England by Lloyd Morgan. Weismann’s contention that inherent characters are alone transmissible by heredity has also received strong support from the immense body of Cytological, Mendelian, and Mutationist work to which other addresses to be delivered to-day will bear eloquent testimony.! Finally, the flourishing school of American Psy- chology, under the leadership of William James and James Mark Baldwin, accepts, and in accept- ing helps to confirm, the theory of Natural Selection. ERASMUS DARWIN AND LAMARCK Professor Henry F. Osborn, in his interesting work, From the Greeks to Darwin, concludes that Lamarck was unaware of Erasmus Darwin’s Zoo- nomia, and that the parallelism of thought is a coincidence.2 The following passage from 1 The addresses referred to are published in Fifty Years of Darwinism, New York, Henry Holt and Company, 1909. 2 From the Greeks to Darwin, New York, 1894, 152-5. Professor Osborn shows on p. 145 that Erasmus Darwin made use of the term B2 4 FIFTY YEARS OF DARWINISM a letter! written to Huxley, probably in 1859, and published since the appearance of Professor Osborn’s book, indicates that Charles Darwin suspected the French naturalist of borrowing from his grandfather :— ‘The history of error is quite unimportant, but it is curious to observe how exactly and accurately my grandfather (in Zoonomia, vol. iL, p. 504, 1794) gives Lamarck’s theory. I will quote one sentence. Speaking of birds’ beaks, he says: “All which seem to have been gradually produced during many generations by the perpetual endeavour of the creatures to supply the want of food, and to have been delivered to their posterity with constant improvement of them for the purposes required.” Lamarck published Hist. Zoolog. in 1809. The Zoonomia was translated into many languages.’ A careful comparison of the French transla- tion of the Zoonomia with Lamarck’s Philosophie Zoologique and with a preliminary statement of his views published in 1802, would probably decide this interesting question. THE INFLUENCE OF LYELL UPON CHARLES DARWIN The limits of space compel me to pass by the youth of Charles Darwin, with the influence of school, Edinburgh and Cambridge, including his intimacy with Henslow—a friendship leading to the voyage in the Beagle. We must also pass by his earliest convictions on evolution, the ‘acquired’ in the sense of ‘acquired characters’; ‘changement acquis’ is the form employed many years later by Lamarck. More Letters of Charles Darwin. Edited by Francis Darwin and ; Me Seward, London, 1903, i. 125. Hereafter quoted as More ellers. DARWIN’S DEBT TO LYELL 5 first note-book begun in 1837, the reading of Malthus and discovery of Natural Selection in October, 1838, the imperfect sketch of 1842, the completed sketch of 1844. It is necessary, however, to pause for a brief consideration of the influence of Sir Charles Lyell. Although the writings of the illustrious geologist have always been looked upon as among the chief of the forces brought to bear upon the mind of Darwin, evidence derived from the later volumes of correspondence justifies the belief that the effect was even greater and more signi- ficant than has been supposed. Huxley has maintained with great force that the way was paved for Darwin by Lyell’s Principles of Geology far more thoroughly than by any other work. ‘, . . consistent uniformitarianism postulates evolution as much in the organic as in the inorganic world. The origin of a new species by other than natural agencies would be a vastly greater “ catastrophe ” than any of those which Lyell successfully eliminated from sober geological specula- tion.’ When the first volume of the Principles appeared in 1830, Darwin was advised by Henslow to obtain and study it, ‘but on no account to accept the views therein advocated.’ Darwin took the volume with him on the voyage, and a study of the very first place at which the Beagle touched, 1 Life and Letters of Charles Darwin, edited by Francis Darwin, London, 1887, ii. 190. Hereafter quoted as Life and Letters. 6 FIFTY YEARS OF DARWINISM St. Jago, one of the Cape de Verde Islands, showed him the infinite superiority of Lyell’s teachings.? He wrote in 1876: ‘The science of Geology is enormously indebted to Lyell—more so, as I believe, than to any other man who ever lived.’? An even more remarkable tribute to his old teacher is paid by Darwin in the following words written to L. Horner, August 29, 1844 :— ‘IT have lately been reading with care A. d’Orbigny’s work on South America, and I cannot say how forcibly impressed I am with the infinite superiority of the Lyellian school of Geology over the continental. I always feel as if my books came half out of Lyell’s brain, and that I never acknowledge this sufficiently ; nor do I know how I can without saying so in so many words—for I have always thought that the great merit of the Principles was that it altered the whole tone of one’s mind, and therefore that, when seeing a thing never seen by Lyell, one yet saw it partially through his eyes—it would have been in some respects better if I had done this less... .’* This letter was written not two months after the date which marks the completion of the finished sketch of 1844. On July 5, Darwin wrote the letter to his wife begging her, in the event of his death, to arrange for the publication of the account he had just prepared. At this psychological moment in his career he wrote of the influence received from Lyell, and we are naturally led to observe how essentially Lyellian 1 Life and Letters, i. 62, 72, 73. 2 l.e., 72. 3 More Letters, ii. 117. LYELL’S DEBT TO DARWIN ; 7 are the three lines of argument—two based on geographical distribution, one on the relation between the living and the dead—which first led Darwin toward a belief in evolution. The thoughts which shook the world arose in a mind whose whole tone had been altered by Lyell’s teachings. Inasmuch as the founder of modern geology received his first inspiration from Buckland, Oxford may claim some share in moulding the mind of Darwin." It is deeply interesting to set beside the evidence of Darwin’s debt to Lyell the words in which Lyell gives us some conception of what Darwin’s friendship—even in its early days— meant for him. Not long after Darwin’s mar- riage (Jan. 29, 1889), when he and his wife were contemplating leaving London for the country, Lyell wrote :— ‘TI cannot tell you how often since your long illness I have missed the friendly intercourse which we had so frequently before, and on which I built more than ever after your marriage. It will not happen easily that twice in one’s life, even in the large world of London, a congenial soul so occupied with precisely the same pursuits and with an independence enabling him to pursue them will fall so nearly in my way, and to have had it snatched from me with the prospect of your residence somewhat far off is a privation I feel to be a very great one.’? 1 See also pp. 86, 87. . 2 July ?, 18419. More Letters, i. 31. Darwin left London for Down on Sept. 14, 1842. 8 FIFTY YEARS OF DARWINISM ‘COMING EVENTS CAST THEIR SHADOWS BEFORE’ The characteristic feature in which Natural Selection differs from every other attempt to solve the problem of evolution is the account taken of the struggle for existence, and the réle assigned to it. Professor Osborn! refers to the keen appreciation of this struggle in Tennyson’s noble poem, In Memoriam, the dedication of which is dated 1849, ten years before the Origin. The poet is disquieted by :— “Nature red in tooth and claw With ravine,.........- 4 and by ‘, .. finding that of fifty seeds She often brings but one to bear.’ It is interesting to note that the obvious under- statement of this last passage is corrected in the author’s notes published by his son a few years ago. In these we find ‘for fifty, read myriad’. The poignant sense of the waste of individual lives is brought into close relation in the poem with the destruction of the type or species :— ‘So careful of the type she seems, So careless of the single life ;’ ‘“ “So careful of the type?” but no, From scarped cliff and quarried stone She cries “ A thousand types are gone: I care for nothing, all shall go”.’ ' From the Greeks to Darwin, New York, 1894, 141. TENNYSON AND THE ‘ORIGIN’ 9 In this association between the struggle for existence waged by individuals and the extinction and succession of species we seem to approach the central idea of Darwin and Wallace. A few years before Tennyson’s death I asked Dr. Grove, of Newport, in the Isle of Wight, if he would point out the parallelism, so far as it existed, to his illustrious patient, hoping that some light might be thrown on the source of the inspiration. Nor was I disappointed. ‘Stay,’ said the aged poet when Dr. Grove had spoken, ‘In Memoriam was published long before the Origin of Species.’ ‘Oh! then you are the man,’ replied the doctor. ‘Yes, I am the man.’ There was silence for a time; then Tennyson said: ‘I don’t want you to go away with a wrong impression. The fact is that long before Darwin’s work appeared these ideas were known and talked about.’ From this deeply interesting conversation I think it is probable that, perhaps through mutual friends, some echo of Darwin’s researches and thoughts had reached the great author of In Memoriam. The light which has been recently thrown? upon Philip Gosse’s remarkable book, Omphalos, indicates that its appearance in 1858 was connected with the thoughts that were to arouse 1 In a valuable letter on Darwin and Tennyson in The Spectator for Aug. 7, 1909 (pp. 197, 198), the Rev. F. St. John Thackeray points out that the poet was from his youth deeply interested in evolution, and that in 1837 he studied Lyell’s Principles. It is shown above, however, that the appreciation of the struggle for existence is an essentially Darwinian idea. 2 In Father and Son, London, 1907. 10 FIFTY YEARS OF DARWINISM the world in the following year. The author of Omphalos was a keen and enthusiastic naturalist held fast in the grip of the narrowest of religious creeds. We learn with great interest that he and others were by Layell’s advice prepared beforehand for the central thoughts of the Origin. To the new teaching all the naturalist side of his nature responded, but from it the religious side recoiled. Religion conquered in the strife, but the naturalist found comfort in the perfectly logical conclusion that : — ‘any breach in the circular course of nature could be con- ceived only on the supposition that the object created bore false witness to past processes, which had never taken place.’ ' Thus the divergence between the literal inter- pretation of Scripture and the conclusions of both geologist and evolutionist were for this remarkable man reconciled by the conviction :— ‘that there had been no gradual modification of the surface of the earth, or slow development of organic forms, but that when the catastrophic act of creation took place, the world presented, instantly, the structural appearance of a planet on which life had long existed.’? Philip Gosse could not but believe that the thoughts which had brought so much comfort to himself would prove a blessing to others also. He offered Omphalos ‘with a glowing gesture, to atheists and Christians alike. . . . But, alas! atheists and Christians alike looked at it and laughed, and threw it away’? Charles Kingsley 11 e., 120, 121. * le. 120, 5 le, 122, THE CREATION OF FALSE WITNESS 11 expressed the objection felt by the Christian when he wrote that he could not ‘believe that God had written on the rocks one enormous and super- fluous lie’! About twenty years ago I was present when precisely the same conclusion was advanced by a high dignitary of the English Church. He argued that even if the history of the Universe were carried back to a single element such as hydrogen, the human mind would remain unsatis- fied and would inquire whence the hydrogen came, and that any and every underlying form of mat- ter must leave the inexorable question ‘ whence?’ still unanswered. Therefore if in the end the question must be given up, we may as well, he argued, admit the mystery of creation in the later stages as in the earlier. Thus he arrived at the belief in a world formed instantaneously, ready-made and complete, with its fossils, marks of denudation, and evidences of evolution —a going concern. Aubrey Moore, the clergyman who more than any other man was responsible for breaking down the antagonism towards evolution then widely felt in the English Church, replied very much as Kingsley had done, that he was unwilling to believe that the Creator had de- liberately cheated the intellectual powers He had 1 Tbid. It is possible that Darwin was referring to Omphalos when he wrote, Sept. 2, 1859, to Lyell, ‘our posterity will marvel as much about the current belief as we do about fossil shells having been thought to have been created as we now see them.’ Life and Letters, ii. 165. 12 FIFTY YEARS OF DARWINISM made. I may add that, inasmuch as science con- sists in the attempt to carry down causation as far as possible, it is above all the scientific side of the human intellect that is outraged—no weaker term can be used—by this more modern develop- ment of the argument of Omphalos. THE PUBLICATION OF THE DARWIN-WALLACE ESSAY In May, 1856, Darwin, urged by Lyell, began to prepare for publication. He had determined to present his conclusions in a volume, for he was unwilling to place any responsibility for his opinions on the Council of a Scientific Society. On this point, he was, as he told Sir Joseph Hooker, in the only fit state for asking advice, namely, with his mind firmly made up: ‘then . . . good advice was very comfortable, and it was easy to reject bad advice.’!| The work was con- tinued steadily until June 18, 1858, when Wal- lace’s letter and essay arrived from Ternate. As a result of the anniversary held in London on July 1, 1908, new light has been thrown upon the circumstances under which the joint essay was published fifty years before. In consequence of the death of the eminent botanist, Robert Brown, Vice-President and Ex- President of the Linnean Society, the last meeting of the summer session, called for June 17, was adjourned. The bye-laws required that the 1 Life and Letters, ii. 70. See also 68, 69, 71. THE EVENTS OF JULY 1, 1858 13 vacancy on the Council should be filled up within three months, and a special meeting was called for July 1 for this purpose. Darwin received Wallace’s essay on June 18, too late for the summer meetings of the Society, but in good time for Lyell and Hooker to present it to the special meeting. Hence, as Sir Joseph Hooker said on July 1, 1908, the death of Robert Brown caused the theory of Natural Selection to be ‘given to the world at least four months earlier than would otherwise have been the case’. Sir Joseph Hooker also informed us that from June 18, up to the evening of July 1, when he met Sir Charles Lyell at the Society, all the intercourse with Darwin and with each other was conducted by letter, and that no fourth person was admitted into their confidence. The joint essay was read by the Secretary of the Society. Darwin was not present, but both Lyell and Hooker ‘said a few words to emphasise the importance of the subject’! Among those who were present were Oliver, Fitton, Carpenter, Henfrey, Burchell, and Bentham,’ who was elected ‘ Darwin-Wallace Celebration of the Linnean Society of London (1908), 14, 15. ; : : 2 July 1, 1858, was an important date in the life of the great botanist George Bentham. He had himself prepared for that very meeting a long paper illustrating what he believed to be the fixity of species. ‘Most fortunately my paper had to give way to Mr. Darwin’s, and when once that was read, I felt bound to defer mine for reconsideration; I began to entertain doubts on the subject, and on the appearance of the “ Origin of Species”, I was forced, however reluctantly, to give up my long-cherished con- victions, the results of much labour and study, and I cancelled all that part of my paper which urged original fixity.’ Life and Letters, ii, 294. See also the Quarterly Review (July, 1909), 6. 14 FIFTY YEARS OF DARWINISM on the Council and nominated as Vice-President in place of Robert Brown. I cannot resist the temptation to reprint from the memorial volume issued by the Linnean Society of London some passages in the address which A, R. Wallace felt constrained to deliver on July 1, 1908, protesting against the too great credit which he believed had been assigned to himself. After describing Darwin’s discovery of Natural Selection and the twenty years devoted to confirmation and patient research, Wallace continued :— ‘How different from this long study and preparation— this philosophic caution—this determination not to make known his fruitful conception till he could back it up by overwhelming proofs—was my own conduct. The idea came to me, as it had come to Darwin, in a sudden flash of insight: it was thought out in a few hours—was written down with such a sketch of its various applications and developments as occurred to me at the moment,—then copied on thin letter-paper and sent off to Darwin—all with- in one week. J was then (as often since) the “‘ young man in a hurry”: he, the painstaking and patient student, seek- ing ever the full demonstration of the truth that he had discovered, rather than to achieve immediate personal fame. ‘Such being the actual facts of the case, I should have had no cause for complaint if the respective shares of Darwin and myself in regard to the elucidation of nature’s method of organic development had been thenceforth estimated as being, roughly, proportional to the time we had each bestowed upon it when it was thus first given to the world—that is to say, as 20 years is to one week. For, he had already made it his own. If the persuasion of his friends had prevailed with him, and he had published WALLACE’S WORDS ON JULY 1, 1908 15 his theory, after 10 years’—15 years’—or even 18 years’ elaboration of it—Z should have had no part in it what- ever, and he would have been at once recognised, and should be ever recognised, as the sole and undisputed dis- coverer and patient investigator of the great law of ‘‘ Natural Selection ” in all its far-reaching consequences. ‘It was really a singular piece of good luck that gave me any share whatever in the discovery. .. it was only Darwin’s extreme desire to perfect his work that allowed me to come in, as a very bad second, in the truly Olympian race in which all philosophical biologists, from Buffon and Erasmus Darwin to Richard Owen and Robert Chambers, were more or less actively engaged.’ ? ECHOES OF THE STORM It is impossible to do more than refer briefly to the storm of opposition with which the Origin was at first received. The reviewer in the Athenaeum for Nov. 19, 1859, left the author ‘to the mercies of the Divinity Hall, the Col- lege, the Lecture Room, and the Museum’? Dr. Whewell for some years refused to allow a copy of the Origin to be placed in the library of Trinity College, Cambridge.? My predecessor, Professor J. O. Westwood, proposed to the last Oxford University Commission the permanent endowment of a lecturer to combat the errors of Darwinism. ‘Lyell had difficulty in prevent- ing [Sir William] Dawson reviewing the Origin on hearsay, without having looked at it. No spirit of fairness can be expected from so biassed ' Darwin-Wallace Celebration of the Linnean Society of London (1908), 6, 7. i" 2 Life and Letters, ii, 228 n. 5 Tbid., 261 1. 16 FIFTY YEARS OF DARWINISM a judge.’* And even when naturalists began to be shaken by the force of Darwin’s reasoning, they were often afraid to own it. Thus Darwin wrote to H. Fawcett, on Sept. 18, 1861 :— ‘Many are so fearful of speaking out. A German naturalist came here the other day; and he tells me that there are many in Germany on our side, but that all seem fearful of speaking out, and waiting for some one to speak, and then many will follow. The naturalists seem as timid as young ladies should be, about their scientific reputation.’ ” Among the commonest criticisms in the early days, and one that Darwin felt acutely,? was the assertion that he had deserted the true method of scientific investigation. One of the best exam- ples of this is to be found in the letter of Darwin’s old teacher in geology, Adam Sedgwick :— ‘You have deserted—after a start in that tram-road of all solid physical truth—the true method of induction, and started us in machinery as wild, I think, as Bishop Wilkins’s locomotive that was to sail with us to the moon.’ 4 This ill-aimed criticism was soon set to rest by Henry Faweett’s article in Macmillan’s Magazine 1 From a letter written by Darwin to Hooker, Nov. 4, 1862. More Letters, i. 468. 2 More Letters, i. 196. 8 See Darwin’s letter to Henslow, May 8, 1860. More Letters, i. 149, 150. * Life and Letters, ii. 248. Sedgwick’s letter is dated Dec. 24, 1859, but the editors of More Letters (i. 150.) express the opinion that it must have been written in November at latest. See also the Quarterly Review for July, 1860. Sedgwick’s review in the Spectator, Mar. 24, 1860, contains the following passage: «”.. 1 cannot conclude without expressing my detestation of the theory, because of its unflinching materialism ;—because it has deserted the inductive track, the only track that leads to physical truth ;—because it utterly repudiates final causes, and thereby indicates a demoralised understanding on the part of its advocates.’ Quoted in Life and Letters, ii. 298. SUPPORT BY MILL AND FAWCETT 17 in 1860, and by a paper read before the British Association by the same author in 1861. _Refer- ring to this defence Fawcett wrote to Darwin, July 16, 1861 :— ‘TI was particularly anxious to point out that the method of investigation pursued was in every respect philosophically correct. I was spending an evening last week with my friend Mr. John Stuart Mill, and I am sure you will be pleased to hear from such an authority that he considers that your reasoning throughout is in the most exact accord- ance with the strict principles of logic. He also says the method of investigation you have followed is the only one proper to such a subject. ‘Tt is easy for an antagonistic reviewer, when he finds it difficult to answer your arguments, to attempt to dispose of the whole matter by uttering some such commonplace as “This is not a Baconian induction”. ... ‘As far as I am personally concerned, I am sure I ought to be grateful to you, for since my accident nothing has given me so much pleasure as the perusal of your book. Such studies are now a great resource to me.’ ! To this Darwin replied :— ‘You could not possibly have told me anything which would have given me more satisfaction than what you say about Mr. Mill’s opinion. Until your review appeared I began to think that perhaps I did not understand at all how to reason scientifically.’ * In the general truth of his theory Darwin felt an entire confidence born of the long years of pondering over difficulties throughout the whole realm of natural history. And it was the con- sciousness that a secure and undisturbed belief lay behind the fair and cautious statements of the 1 More Letters, i. 189, 190. 2 Tbid., 189. Cc 18 FIFTY YEARS OF DARWINISM Origin that was so intensely irritating to men whose antagonism was based on religious con- viction. Thus in Sedgwick’s letter, from which I have already quoted, we read :— ‘Lastly, then, I greatly dislike the concluding chapter— not as a summary, for in that light it appears good—but I dislike it from the tone of triumphant confidence in which you appeal to the rising generation . .. and prophecy of things not yet in the womb of time, nor (if we are to trust the accumulated experience of human sense and the inferences of its logic) ever likely to be found anywhere but in the fertile womb of man’s imagination.’! THE MATURITY OF THE ORIGIN CONTRASTED WITH THE CRUDITY OF RIVAL INTERPRETATIONS It is remarkable to contrast the maturity, the balance, the judgement, with which Darwin put forward his views, with the rash and haphazard objections and rival suggestions advanced by critics. It is doubtful whether so striking a con- trast is to be found in the history of science— on the one side, twenty years of thought and investigation pursued by the greatest of natura- lists; on the other, off-hand impressions upon a most complex problem hastily studied. and usually very imperfectly understood. It is not to be wondered at that Darwin found the early criticisms so entirely worthless. The following extract from an interesting letter to John Scott, 1 Life and Letters, ii. 250. RASHNESS OF RIVAL HYPOTHESES 19 written on Dec. 3, 1862?, shows how well aware he was of difficulties unnoticed by critics :— “ You speak of difficulties on Natural Selection: there are indeed plenty ; if ever you have spare time (which is not likely, as Iam sure you must be a hardworker) I should bevery glad to hear difficulties from one who has observed so much as you have. The majority of criticisms on the Origin are, in my opinion, not worth the paper they are printed on,’! From the very first the most extraordinarily crude and ill-considered suggestions were put for- ward by those who were unable to recognize the value of the theory of Natural Selection. A good example is to be found in Andrew Murray’s principle of sexual selection based on contrast :— ‘It is trite to a proverb, that tall men marry little women ... aman of genius marries a fool... and we are told that this is the result of the charm of contrast, or of qualities admired in others because we do not possess them. I do not so explain it. I imagine it is the effort of nature to preserve the typical medium of the race.’? Even in these later years the wildest imagin- ings may be put forward in all seriousness as the interpretation of the world of living organisms. Thus in Beccari’s interesting work on Borneo,’ the author compares the infancy and growth of the organic world with the development and education of an individual. In youth the indi- vidual learns easily, being unimpeded by the 1 More Letters, ii. 311. . 2 Life and Letters, ii. 261. The original paper is to be found in the Proc. R. Soc. Edin., 1860. 3 Wanderings in the Great Forests of Borneo, 209-16, English translation, London, 1904. ce 20 ‘FIFTY YEARS OF DARWINISM force of habits, while ‘with age heredity acts more strongly, instincts prevail, and adaptation to new conditions of existence and to new ideas become more difficult ; in a word, it is much less easy to combat hereditary tendencies ’. Similarly, in the state of maturity now reached by the organic world, Beccari believes that the power of adaptation is wellnigh non-existent. Heredity, through long accumulation in the course of endless generations, has become so powerful that species are now stereotyped and cannot undergo advan- tageous changes. For the same reason, he con- siders, acquired characters cannot now be trans- mitted to offspring. Beccari imagines that everything was different in early ages, when, as he supposes, life was young and heredity weak. In this assumed ‘ Plasmatic Epoch’ the environ- ment acted strongly upon organisms, evoking the responsive changes which have now been ren- dered fixed and immovable by heredity. Even the hypothesis proposed as a substitute for Natural Selection by so distinguished a botanist as Carl Nageli turns out to be most unsatisfactory the moment it is examined. The idea of evolution under the compulsion of an internal force residing in the idioplasm is in essence but little removed from special creation. On the subject of Nigeli’s criticisms Darwin wrote, Aug. 10, 1869, to Lord Farrer :— ‘It is to me delightful to see what appears a mere morpho- logical character found to be of use. It pleases me the more DARWIN’S DEBT TO HOOKER 21 as Carl Nageli has lately been pitching into me on this head. Hooker, with whom I discussed the subject, maintained that uses would be found for lots more structures, and cheered me by throwing my own orchids into my teeth.’ * DARWIN’S GREATEST FRIENDS IN THE TIME OF STRESS It is interesting to put side by side passages from two letters? written by Darwin to Hooker, one in 1845 at the beginning of their friendship, the other thirty-six years later, a few months before Darwin’s death. The first shows the instant growth of their friendship: ‘Farewell ! What a good thing is community of tastes! I feel as if I had known you for fifty years. Adios.’ The second letter expresses at the end of Darwin’s life the same feelings which find utterance ever and again throughout the long years of his friendship (see pp. 66, 67). ‘Your letter has cheered me, and the world does not look a quarter so black this morning as it did when I wrote before. Your friendly words are worth their weight in gold.’ It was to Hooker that Darwin first confided, Jan. 11, 1844, his belief in evolution, but did not at the time, even to him, give any account of natural selection :— ‘At last gleams of light have come, and I am almost convinced (quite contrary to the opinion I started with) that 1 More Letters, ii. 380. : ; 2 Tbid., i. 39. The passages here quoted are placed side by side by the editors of this work. 22 FIFTY YEARS OF DARWINISM species are not (it is like confessing a murder) immutable. . .. I think I have found out (here’s presumption !) the simple way by which species become exquisitely adapted to various ends. You will now groan, and think to yourself, ‘on what a man have I been wasting my time and writing to.” I should, five years ago, have thought so. ..’? Elaborate investigations of all kinds during the long years which led up to the central work of Darwin’s life were discussed in detail with the greatest of his friends, and it was an inestimable advantage that the ideas of the Origin were thus searchingly tried beforehand by so critical and, in the best sense, sceptical a mind as Hooker’s— ‘you terrible worrier of poor theorists!’? as Darwin called him. Again in 1868 :— ‘IT have got your photograph over my chimney-piece, and like it much; but you look down so sharp on me that I shall never be bold enough to wriggle myself out of any contradiction.’ ® The friendship with Asa Gray began with a meeting at Kew some years before the publication of Natural Selection. Darwin soon began to ask for help in the work which was ultimately to appear as the Origin. The following letter to Hooker, June 10, 1855, shows what he thought of the great American botanist :— ‘I have written him a very long letter, telling him some of 1 Life and Letters, ii. 28, 24. See also on p. 32 the letter, dated Oct. 12, [1845], in which Darwin confided his belief ‘that species are mutable’ tothe Rev. L. Jenyns (Blomefield). The passage from a letter dated Feb. 14, 1845, to the same correspondent, quoted on p. 42 n. 1, suggests that the communication of Oct. 12 was written in 1844 and not 1845, * Feb. 28, [1858]. More Letters, i. 105. 3 More Letters, ii. 376, 377. DARWIN’S DEBT TO ASA GRAY 23 the points about which I should feel curious. But on my life it is sublimely ridiculous, my making suggestions to such a man.”! ‘The friendship ripened very quickly, so that on July 20, 1856, Darwin gave Asa Gray an account of his views on evolution,? and on Sept. 5 of the following year, a tolerably full description of Natural Selection. From this last letter Darwin chose the extracts which formed part of his section of the joint essay published July 1, 1858. Asa Gray’s opinion on first reading the Origin was expressed not to Darwin but to Hooker in a letter written Jan. 5, 1860 :— ‘It is done in a masterly manner. It might well have taken twenty years to produce it. It is crammed full of most interesting matter—thoroughly digested—well ex- pressed—close, cogent, and taken as a system it makes out a better case than I had supposed possible. .. .’ After referring to Agassiz’s unfavourable opinion of the book he continues: ‘Tell Darwin all this. I will write to him when I get a chance. As I have promised, he and you shall have fair-play here... .’* A little later, when on Jan. 23 he wrote to Darwin himself, Asa Gray concluded: ‘I am free to say that I never learnt so much from one book as I have from yours. There remain a thousand things I long to say about it.’ ® 1 More Letters, i. 418. Asa Gray's generous reply appears on p. 421. 2 Life and Letters, ii. 78. 8 Thid., 120-5. - 4 Tbid., 268. 5 Ibid., 272. 24 FIFTY YEARS OF DARWINISM It is impossible to do justice on the present occasion to the numerous letters in which Darwin expressed his gratitude for the splendid manner in which Asa Gray kept his word and fought ‘like a hero in defence’! At a time when few naturalists were able to understand the drift of Darwin’s argument, the acute and penetrating mind of Asa Gray had in a moment mastered every detail. Thus Darwin wrote on July 22, 1860, concerning the article in the Proceedings of the American Academy for April 10 :— ‘,.. I cannot resist expressing my sincere admiration for your most clear powers of reasoning. As Hooker lately said in a note to me, you are more than any one else the thorough master of the subject. I declare that you know my book as well as I do myself; and bring to the question new lines of illustration and argument in a manner which excites my astonishment and almost my envy!... Every single word seems weighed carefully, and tells like a 32-pound shot.’ ? Some weeks later, on Sept. 26, 1860, Darwin again expressed the same admiration, and stated that Asa Gray understood him more perfectly than any other friend :— “, . » you never touch the subject without making it clearer. I look at it as even more extraordinary that you never say 2 word or use an epithet which does not express fully my meaning. Now Lyell, Hooker, and others, who perfectly understand my book, yet sometimes use expressions to which I demur.’$ 1 Life and Letters, i ae waa ais 2 Thid., 326. id., 344, 345. DARWIN’S DEBT TO HUXLEY 25 Darwin also sent! Asa Gray’s defence of the Origin to Sir Charles Lyell, whom he was extremely anxious to convince of the truth of evolution. Asa Gray’s religious convictions prevented the full acceptance of Natural Selection. He was ever inclined to believe in the Providen- tial guidance of the stream of variation. He also apparently differed from Darwin in the extent to which he was inclined to interpret instincts as inherited habits.? The same close intimacy and mutual help begun in the preparation of the Origin was continued in Darwin’s later botanical works. Thus Darwin owed his Climbing Plants to the study of a paper by Asa Gray, and he dedicated his Forms of Flowers to the American botanist ‘as a small tribute of respect and affection’. Concerning some of the researches which afterwards appeared in this book, Darwin wrote :— ‘I care more for your and Hooker’s opinion than for that of all the rest of the world, and for Lyell’s on geological points.’ § Another great name, that of Huxley, is especially associated in our minds with the defeat of those who would have denied that the subject was a proper one for scientific investiga- tion. In the strenuous and memorable years that followed the appearance of the Origin, the mighty warrior stands out as the man to whom 1 More Letters, i. 169. ia a Life and Letters, iii. 170. id., 300. 26 FIFTY YEARS OF DARWINISM more than to any other we owe the gift of free speech and free opinion in science,—the man so admirably described by Sir Ray Lankester at the Linnean Celebration as ‘the great and beloved teacher, the unequalled orator, the brilliant essayist, the unconquerable champion and literary swordsman—Thomas Henry Huxley’.! Comparing the friendships to which Darwin owed so much, Lyell was at first the teacher but finally the pupil,—unwilling and unconvinced at the outset, in the end convinced although still unwilling; Hooker in England and Asa Gray in America were the two intimate friends on whom Darwin chiefly depended for help in writing the Origin, and for support to its arguments ; Huxley was the great general in the field where religious convictions, expressed or unexpressed, were the foundation of a fierce and bitter antagonism. THE ATTACKS OF RICHARD OWEN AND ST. GEORGE MIVART An unnecessary bitterness was imported into the early controversies in England, because of the personality of the scientific leaders in the attacks on the Origin. Of these the chief was the great comparative anatomist, Sir Richard Owen. In spite of his leading scientific position, this remarkable man withdrew from contact with his brother zoologists, living in a self-imposed _isola- 1 Darwin-Wallace Celebration of the Linnean Society of London (1908), 29. See also pp. 66-8 of the present work. THE ATTACKS OF OWEN 27 tion which tended towards envy and bitterness. The same unavailing detachment had _ been carried much further by the great naturalist W. J. Burchell, who, as from a watch-tower, looked upon the world he strove to avoid with an absorbed and jealous interest. Prof. J. M. Baldwin has shown how inevitable and inexorable is the grip of the social environment: the more we attempt to evade it, the more firmly we seem to be held in its grasp. In the first years of the struggle, Owen’s bitter antagonism made itself felt in the part he took as ‘crammer’ to the Bishop of Oxford, and in his anonymous article in the Edinburgh Review for April, 1860. But Owen could not bear to remain apart from the stream of thought when there was no doubt about the way it was flowing, so that in a few years he was maintaining some of the chief conclusions of the Origin, although retracting nothing, but rather keeping up a bitter attack upon Darwin. This treatment received from one who was all affability when they met,' was natu- rally resented by Darwin, whose feelings on the subject are expressed in the following passage from a letter to Asa Gray, July 28, 1862. ‘ By the way, one of my chief enemies (the sole one who has annoyed me), namely Owen, I hear has been lecturing on birds; and admits that all have descended from one, and advances as his own idea that the oceanic wingless birds 1 ‘Mrs, Carlyle said that Owen’s sweetness always reminded her of sugar of lead.’ Life and Letters of T. H. Huxley, London, ii. 167. 28 FIFTY YEARS OF DARWINISM have lost their wings by gradual disuse. He never alludes to me, or only with bitter sneers, and coupled with Buffon and the Vestiges.’! In the historical sketch added to the later editions of the Origin, Owen is the only writer who is severely dealt with. In this introductory section Darwin said that he was unable to decide whether Owen did or did not claim to have originated the theory of Natural Selection.? If Owen had withdrawn from his former attitude of antagonism, as did Lyell, he would be entitled to the same honourable place in the memory of future generations. As it is, we must regret that he did not keep up the struggle to the 1 More Letters, i. 203. 2 Origin of Species, 6th Ed., xviii. See also the writer's article in the Quarterly Review for July, 1909, 4-6. The following remark- able episode, which I owe to the kindness of my friend Mr. Roland Trimen, F.R.S., is quoted from p. 5 :— “At Down, about the end of the year 1867, when conversing with Mr. Darwin about the already steadily increasing acceptance of the “Origin” among thinking naturalists, in contrast to the active hostility it encountered on and long after its first appearance only eight years before, I referred to the heavy artillery brought to bear against it in the “Quarterly” and ‘ ‘Wdinburgh ” Reviews, besides the host of other discharges from arms of minor calibre. Mr. Darwin asked me if I knew who wrote the “‘ Edinburgh ” article, and on my replying that I did not, but that I had heard Owen’ sname suggested amongst others, he said, ““Owen was the man.” I ven- tured to enquire whether he came to this conclusion from other evidence than that afforded by the style, tone, etc., of the article itself; and he answered, ‘‘The internal evidence made me almost sure that only Owen could have written it ; but when I taxed him with the authorship and he absolutely denied it—then I was quite certain.” ‘Words of such keen satire came with extraordinary effect from aman so eminently gentle and considerate, and so free from any touch of jealousy or self-assertion as Darwin. They made a deep and lasting impression on me—all the more because they were spoken very quietly and deliberately, and because they were the only words of censure I heard used by the greatest of naturalists.’ OWEN AND EVOLUTION IN 1881 29 end. How completely he abandoned it, and how sharp was the contrast between him and a still surviving warrior of the ‘Old Guard’, remains as one of my earliest and clearest memories of the scientific world. The stage was the meeting of the British Association at York, in 1881, when Prof. O. C. Marsh described the Berlin skeleton of Archaeopteryx. The lizard-like characteristics of the earlier fossil in the British Museum— bought, it was said, at the price of a dowry for a professor’s daughter—were far more clearly displayed in the later find. Prof. Marsh told me that he would have given almost any sum to secure this—probably the most valuable and interesting fossil in the world—for the museum at Yale. ‘I dare not do it,’ was the reply. ‘We let the other go, and I really believe they would kill me if I sold this one.’ So Prof. Marsh, pbliged to study the wonderful ancestral bird in Berlin, came, fresh from his work, to tell us about it at York. Owen, presiding over the zoological section at which the paper was read, seemed quite enthu- siastic over Archaeopteryx, and had not a word of criticism for the evolutionary history which it unfolded. He discoursed sweetly upon the teeth, believed to have been discovered in embryonic parrots, and, with his suave manner and venerable appearance, created a very pleasant impression. An entirely different scene was enacted, a day or two later, in the geological section, where Prof. 30 FIFTY YEARS OF DARWINISM H. G. Seeley exhibited a restoration of the same fossil. Dr. Wright, the palaeontologist, old and deaf, but staunch as ever, would have none of it. ‘ Archaeopteryx hasn’t got a head. How can it possibly have teeth?’ he asked angrily, thinking of the older specimen in the British Museum. But even in this, the remains -of the head, detached from the body, had been made out by Sir John Evans in a corner of the block of oolite, while the teeth were found scattered over the surface of the stone. Prof. Newton’s emphatic assertion that the bird had teeth left him quite unshaken, and even after Prof. Marsh, called on by the chairman, had drawn their form on the blackboard, and the section was proceeding to other business, Dr. Wright could be heard muttering savagely, ‘Archaeopteryx is a very good bird.’ And its excellence was in his opinion obviously incompatible with reptilian affinity. Disbelief in evolution was with him a matter of faith and could never have been affected by any amount of evidence. About twelve years after the appearance of the Origin, another opponent, St. George Mivart, produced something of the same bitterness as Owen, and for a similar reason. Thus Darwin wrote to Hooker, Sept. 16, 1871, as follows :— ‘You never read such strong letters Mivart wrote to me about respect towards me, begging that I would call on him, ete., ete. ; yet in the Q. Review [July, 1871] he shows the greatest scorn and animosity towards me, and with un- MIVART’S INCONSISTENCY 81 common cleverness says all that is most disagreeable. He makes me the most arrogant, odious beast that ever lived. I cannot understand him ; I suppose that accursed religious bigotry is at the root of it. Of course he is quite at liberty to scorn and hate me, but why take such trouble to express something more than friendship? It has mortified me a good deal.’! On other occasions at a much later date I have myself observed that there was something peculiar about the poise of Mivart’s mind, which seemed ever inclined to pass, with abrupt transition, from the extreme of an unnecessary effusiveness to an unnecessarily extreme antagonism. Mivart’s attack, contained in his book, The Genesis of Species, was effectively dealt with by Chauncey Wright in the North American Review for July, 1871. Darwin was so pleased with this defence that he obtained the author’s permission for an English reprint,? and with further additions it was published as a pamphlet by John Murray in 1871. sb tran Mlng Coririn EO Only a year and a half after the publication of the Origin, we find that Darwin wrote to Bates on the subject which was to provide such striking evidence of the truth of Natural Selection :— ‘I am glad to hear that you have specially attended to “mimetic” analogies—a most curious subject ; I hope you publish on it. I have for a long time wished to know whether what Dr. Collingwood asserts is true—that the most striking cases generally occur between insects inhabit- ing the same country.’? The next letter, written about six months later, reveals the remarkable fact that the illus- trious naturalist who had anticipated Edward Forbes in the explanation of arctic forms on alpine heights,” had also anticipated H. W. Bates in the theory of Mimicry :— ‘What a capital paper yours will be on mimetic re- 1 The letter is dated April 4, 1861. More Letters, i. 183. 2 “Twas forestalled in only one important point, which my vanity has always made me regret, namely, the explanation by means of the Glacial period of the presence of the same species of plants and of some few animals on distant mountain summits and in the arctic regions. This view pleased me so much that I wrote it out in extenso, and I believe that it was read by Hooker some years before E. Forbes published his celebrated memoir on the subject. In the very few points in which we differed, I still think that I was in the right. I have never, of course, alluded in print to my having independently worked out this view.’ Autobiography in Life and Letters, i. 88. 124 THE VALUE OF COLOUR semblances! You will make quite a new subject of it. Ihad thought of such cases as a difficulty ; and once, when corre- sponding with Dr. Collingwood, I thought of your explanation ; but I drove it from my mind, for I felt that I had not knowledge to judge one way or the other. Dr. C., I think, states that the mimetic forms inhabit the same country, but I did not know whether to believe him. What wonderful cases yours seem to be !’! The above passage will probably be as great a surprise to other naturalists as it was to the present writer. It would be very interesting to know whether Collingwood published any state- ments on the subject. His book,? quoted by Darwin in the Descent of Man, is dated 1868. Bates read his paper before the Linnean Society, Nov. 21, 1861, and Darwin’s impressions on hearing it were conveyed in a letter to the author dated Dec. 3 :— ‘Under a general point of view, I am quite convinced (Hooker and Huxley took the same view some months ago) that a philosophic view of nature can solely be driven into naturalists. by treating special subjects as you have done. Under a special point of view, I think you have solved one of the most perplexing problems which could be given to solve.’ * The memoir appeared in the following year, and after reading it Darwin wrote as follows, Nov. 20, 1862 :— ‘,.. In my opinion it is one of the most remarkable and admirable papers I ever read in my life... . I am rejoiced ? The letter is dated Sept. 25, 1861. More Letters, i. 197. ? C. Collingwood, Rambles of a Naturalist on the shores and waters of the China Seas, London, 1868. 3 Life and Letters, ii, 378, DARWIN AND BATES’S MEMOIR 125 that I passed over the whole subject in the Origin, for I should have made a precious mess of it. You have most clearly stated and solved a wonderful problem. . . . Your paper is too good to be largely appreciated by the mob of naturalists without souls; but, rely on it, that it will have lasting value, and I cordially congratulate you on your first great work. You will find, I should think, that Wallace will fully appreciate it.’? Four days later, Nov. 24, Darwin wrote to Hooker on the same subject :— ‘I have now finished this paper . ..; it seems to me admirable. To my mind the act of segregation of varieties into species was never so plainly brought forward, and there are heaps of capital miscellaneous observations.’ ? Darwin was here referring to the tendency of similar varieties of the same species to pair together, and on Nov. 25 he wrote to Bates asking for fuller information on this subject.2 If Bates’s opinion were well founded, Sexual Selection would bear a most important part in the establishment of such species. It must be admitted, however, that the evidence is as yet quite insufficient to establish this conclusion. It is interesting to observe how Darwin at once fixed on the part of Bates’s memoir which seemed to bear upon Sexual Selection. A review of Bates’s theory of Mimicry was contributed by Darwin to the Natural History 1 Life and Letters, ii. 391-3. 2 More Letters, i. 214. 3 More Letters,i. 215. See also parts of Darwin’s letter to Bates in Life and Letters, ii. 392. + See Poulton, Essays on Evolution, 1908, 65, 85-8. 126 THE VALUE OF COLOUR Review? and an account of it is to be found in the Origin and in the Descent of Man.? Darwin continually writes of the value of hypothesis as the inspiration of inquiry. We find an example in his letter to Bates, Nov. 22, 1860: ‘T have an old belief that a good observer really means a good theorist, and I fully expect to find your observations most valuable.’* Darwin’s letter refers to many problems upon which Bates had theorized and observed, but as regards Mimicry itself, the hypothesis was thought out after his return home from the Amazons, when he no longer had the opportunity of testing it by the observation of living Nature. It is by no means improbable that, had he been able to apply this test, Bates would have recognized that his division of butterfly resemblances into two classes—one due to the theory of Mimicry, the other to the influence of local conditions—could not be sustained. Fritz Miiller’s contributions to the problem of Mimicry were all made in S.E. Brazil, and numbers of them were communicated, with other observations on natural history, to Darwin, and by him sent to Professor R. Meldola who published many of the facts. Darwin’s letters to Meldola® contain abundant proofs of his interest in Miller’s work upon Mimicry. One deeply 1 New Ser,, iii. 1863, 219. Ed. 1872, 375-8, 3 Kd. 1874, 323-5. * More Letters, i. 176. 5 Poulton, Charles Darwin and the theory of Natural Selection, Lond. (1896), 199-218. SEXUAL VERSUS NATURAL SELECTION 127 interesting letter’ dated Jan. 23, 1872, proves that Fritz Muller before he originated the theory of Common Warning Colours (Synaposematic Resemblance or Miillerian Mimicry), which will ever be associated with his name, had conceived the idea of the production of mimetic likeness by Sexual Selection. Darwin’s letter to Meldola shows that he was by no means inclined to dismiss the suggestion as worthless, although he considered it daring. ‘You will also see in this letter a strange speculation, which I should not dare to publish, about the appreciation of certain colours being developed in those species which frequently behold other forms similarly ornamented. I do not feel at all sure that this view is as incredible as it may at first appear. Similar ideas have passed through my mind when considering the dull colours of all the organisms which inhabit dull-coloured regions, such as Patagonia and the Galapagos Is.’? A little later, on April 5, he wrote to Professor August Weismann on the same subject :— ‘It may be suspected that even the habit of viewing differently coloured surrounding objects would influence their taste, and Fritz Miller even goes so far as to believe that the sight of gaudy butterflies might influence the taste of distinct species.’ * This remarkable suggestion affords interesting evidence that F, Miller was not satisfied with the sufficiency of Bates’s theory. Nor is this surprising when we think of the numbers of 1 Thid., 201, 202. ? Darwin wrote, Aug. 2, 1871, in very similar terms to Fritz Miller himself. Life and Letters, iii. 151. * Life and Letters, iii. 157. 128 THE VALUE OF COLOUR abundant conspicuous butterflies which he saw exhibiting mimetic likenesses) The common instances in his locality, and indeed everywhere in tropical America, were anything but the hard- pressed struggling forms assumed by the theory of Bates. They belonged to the groups which were themselves mimicked by other butterflies. Fritz Miiller’s suggestion also shows that he did not accept Bates’s alternative explanation of a superficial likeness between models themselves, based on some unknown influence of local physico- chemical forces. At the same time Miller’s own suggestion was subject to this apparently fatal objection, that the Sexual Selection he invoked would tend to produce resemblances in the males rather than the females, while it is well known that when the sexes differ the females are almost invariably more perfectly mimetic than the males and in a high proportion of cases are mimetic while the males are non-mimetic. The difficulty was met several years later by Fritz Miiller’s well-known theory, published in 1879,! and immediately translated by Meldola and brought before the Entomological Society.? Darwin’s letter to Meldola dated June 6, 1879, shows ‘that the first introduction of this new and most suggestive hypothesis into this country was due to the direct influence of Darwin himself, who brought it before the notice of the one man who was likely to appreciate it at its true value ! Kosmos, May, 1879, 100. ® Proc. Ent. Soc. Lond., 1879, xx. MELDOLA AND MULLER’S THEORY 129 and to find the means for its presentation to English naturalists.’! Of the hypothesis itself Darwin wrote, ‘F. Miller’s view of the mutual protection was quite new to me.’? The hypothesis of Miillerian Mimicry was at first strongly opposed. Bates himself could never make up his mind to accept it. As the Fellows were walking out of the meeting at which Professor Meldola explained the hypothesis, an eminent entomolo- gist, now deceased, was heard to say to Bates: ‘It’s a case of save me from my friends!’ The new ideas encountered and still encounter to a great. extent the difficulty that the theory of Bates had so completely penetrated the literature of natural history. The present writer has observed that naturalists who have not thoroughly absorbed the older hypothesis are usually far more impressed by the newer one than are those whose allegiance has already been rendered. The acceptance of Natural Selection itself was at first hindered by similar causes, as Darwin clearly recognized :— ‘If you argue about the non-acceptance of Natural Selection, it seems to me a very striking fact that the New- tonian theory of gravitation, which seems to every one now so certain and plain, was rejected by a man so extraordinarily able as Leibnitz. The truth will not penetrate a preoccupied mind.’ * 1 Charles Darwin and the theory of Natural Selection, 214. 2 Ibid., 218. 8 To Sir J. Hooker, July 28, 1868, More Letters, i. 305. See also. the letter to A. R. Wallace, April 30, 1868, in More Letters, ii. 77, lines 6-8 from top. K 130 THE VALUE OF COLOUR There are many naturalists, especially students of insects, who appear to entertain an inveterate hostility to any theory of Mimicry. Some of them are eager investigators in the fascinating field of geographical distribution, so essential for the study of Mimicry itself. The changes of pattern undergone by a species of Erebia as we follow it over different parts of the mountain ranges of Europe is indeed a most interesting inquiry, but not more so than the differences between e.g. the Acraea johnstoni of S.E. Rhodesia and of Kilimanjaro. A naturalist who is interested by the Erebia should be equally interested by the Acraea; and so he would be if the student of Mimicry did not also record that the characteristics which distinguish the northern from the southern individuals of the African species correspond with the presence, in the north but not in the south, of certain entirely different butterflies. That this additional information should so greatly weaken, in certain minds, the appeal of a favourite study, is a psychological problem of no little interest. This curious antagonism is I believe confined to a few students of insects. Those naturalists who, standing rather farther off, are able to see the bearings of the subject more clearly, will usually admit the general support yielded by an ever-growing mass of observations to the theories of Mimicry propounded by H. W. Bates and Fritz Miller. In like manner Natural Selection itself was in the early days PREJUDICE AGAINST MIMICRY 131 often best understood and most readily accepted by those who were not naturalists. Thus Darwin wrote to D. T. Ansted, Oct. 27, 1860 :— ‘I am often in despair in making the generality of naturalists even comprehend me. Intelligent men who are not naturalists and have not a bigoted idea of the term species, show more clearness of mind.’ ! Even before the Origin appeared Darwin anticipated the first results upon the mind of naturalists. He wrote to Asa Gray, Dec. 21, 1859 :— . ‘I have made up my mind to be well abused; but I think it of importance that my notions should be read by intelligent men, accustomed to scientific argument, though not naturalists. It may seem absurd, but I think such men will drag after them those naturalists who have too firmly fixed in their heads that a species is an entity.’? Mimicry was not only one of the first great departments of zoological knowledge to be studied under the inspiration of Natural Selection, it is still and will always remain one of the most interesting and important of subjects in relation to this theory as well as to evolution. In Mimicry we investigate the effect of environment in its simplest form: we trace the effects of the pattern of a single species upon that of another far removed from it in the scale of classification. When there is reason to believe that the model is an invader from another region and has only recently become an element in the environment 1 More Letters, i, 175. 2 Life and Letters, ii. 245. See also pp. 32-3 of the present work. K2 182 THE VALUE OF COLOUR of the species native to its second home, the problem gains a special interest and fascination.’ We are chiefly dealing with the fleeting and changeable element of colour, and we expect to find and we do find evidence of a comparatively rapid evolution. The invasion of a fresh model is for certain species an unusually sudden change in the forces of the environment, and in some instances we have grounds for the belief that the mimetic response has not been long delayed. wf MIMICRY AND SEX Ever since Wallace’s classical memoir on Mimicry in the Malayan swallow-tail butterflies, those naturalists who have written on the subject have followed his interpretation of the marked prevalence of mimetic resemblance in the female sex as compared with the male. They have believed with Wallace that the greater dangers of the female, with slower flight and often alighting for oviposition, have been in part met by the high development of this special mode of protection. The fact cannot be doubted. It is extremely common for a non-mimetic male to be accom- panied by a beautifully mimetic female and often by two or three different forms of female, each mimicking a different model. Indeed in these latter cases the male is usually non-mimetic (e. g. Papilio dardanus=merope), or if a mimic 1 See pp. 159-77, which are devoted to the detailed considera- tion of an example of this kind. WALLACE AND FEMALE MIMICRY 133 (e.g. the Nymphaline genus Euripus) resembles a very different model. On the other hand, a non-mimetic female accompanied by a mimetic male is excessively rare. An example is afforded by the Oriental Nymphaline, Cethosia, in which the males of some species are rough mimics of the brown Danaines. When both sexes mimic, it is very common for the females to be better and often far better mimics than the males. Predominant female Mimicry is character- istic of butterflies and very rare in moths. If examples occur at all among the numberless mimetic Diptera, Coleoptera, &c., they are probably excessively scarce. In some of the orb- weaving spiders, however, the males mimic ants, while the much larger females are non-mimetic. Although still believing that Wallace's hypothesis in large part accounts for the facts briefly summarized above, the present writer has recently been led to doubt whether it offers a complete explanation. Mimicry in the male, even though less beneficial to the species than Mimicry in the female, would still surely be advantageous. Why then is it so often entirely restricted to the female? While the attempt to find an answer to this question was haunting me, I re-read a letter written by Darwin to Wallace, April 15, 1868, containing the following sentences :— ‘When female butterflies are more brilliant than their males you believe that they have in most cases, or in all 184 THE VALUE OF COLOUR cases, been rendered brilliant so as to mimic some other species, and thus escape danger. But can you account for the males not having been rendered equally brilliant and equally protected? Although it may be most for the welfare of the species that the female should be protected, yet it would be some advantage, certainly no disadvantage, for the unfortunate male to enjoy an equal immunity from danger. For my part, I should say that the female alone had happened to vary in the right manner, and that the beneficial variations had been transmitted to the same sex alone. Believing in this, I can see no improbability (but from analogy of domestic animals a strong probability) that variations leading to beauty must often have occurred in the males alone, and been transmitted to that sex alone. Thus I should account in many cases for the greater beauty of the male over the female, without the need of the protective principle.’* The consideration of the facts of Mimicry thus led Darwin to the conclusion that the female happens to vary in the right manner more commonly than the male, while the secondary sexual characters of males supported the conviction ‘that from some unknown cause such characters [viz. new charac- ters arising in one sex and transmitted to it alone] apparently appear oftener in the male than in the female ’.? Comparing these conflicting arguments, we are 1 More Letters, ii. 73, 74. On the same subject—‘the gay- coloured females of Pieris’ (Perrhybris (Mylothris) pyrrha of Brazil), Darwin wrote to Wallace, May 5, 1868, as follows: ‘1 believe I quite follow you in believing that the colours are wholly due to mimicry ; and I further believe that the male is not brilliant from not having received through inheritance colour from the female, and from not himself having varied; in short, that he has not been influenced by selection.’ It should be noted that the male of this species does exhibit a mimetic pattern on the under surface.—More Letters, ii. 78. : poles from Darwin to Wallace, May 5, 1867, More Letters, ii. 61. DARWIN AND FEMALE MIMICRY 135 led to believe that the first is the stronger. ‘Mimicry in the male would be no disadvantage but an advantage, and when it appears would be and is taken advantage of by selection. The -secondary sexual characters of males would be no advantage but a disadvantage to females, and, as “Wallace thinks, are withheld from this sex by selection. It is indeed possible that Mimicry has been hindered and often prevented from passing to the males by Sexual Selection. We know that Darwin was much impressed! by Thomas Belt’s daring and brilliant suggestion that the white patches which exist, although ordinarily concealed, on the wings of mimetic males of certain Pierinae (Dismorphia), have been preserved by preferential mating. He supposed this result to have been brought about by the females exhibiting a deep- seated preference for males that displayed the chief ancestral colour, inherited from periods before any mimetic pattern had been evolved in the species. But it has always appeared to me that Belt’s deeply interesting suggestion requires much solid evidence and repeated confirmation before it can be accepted as a valid interpretation of the facts. In the present state of our knowledge, at any rate of insects and especially of Lepidoptera, it is pro- bable that the female is more apt to vary than the male, and that an important element in the inter- pretation of prevalent female Mimicry is provided 1 Descent of Man, 325. 136 THE VALUE OF COLOUR by this fact. In order adequately to discuss the question of Mimicry and sex it would be necessary to analyse the whole of the facts, so far as they are known in butterflies. On the present occasion it is only possible to state the inferences which have been drawn from general impressions—in- ferences which it is believed will be sustained by future detailed inquiry. (1) Mimicry may occasionally arise in one sex because the differences which distinguish it from the other sex happen to be such as to afford a starting-point for the resemblance. Here the male is at no disadvantage as compared with the female, and the rarity of Mimicry in the male alone (e.g. Cethosia) is evidence that the great predominance of female Mimicry is not to be thus explained. (2) The greater colour-variability of the female, observed at least in certain groups of butterflies, and especially her more pronounced tendency to dimorphism and polymorphism, have been of much importance in determining this pre- dominance. Thus if the female appear in two different forms and the male in only one, it will be twice as probable that she will happen to possess a sufficient foundation for the evolution of Mimicry. (3) The appearance of melanic or partially melanic forms in the female has been of very great service, providing as it does a change of ground-colour. Thus the Mimicry of the black CONCLUSIONS ON MIMICRY AND SEX § 187 generally red-marked American ‘ Aristolochia swallow-tails’ (Pharmacophagus) by the females of Papilio swallow-tails was probably begun in this way. (4) It is probably incorrect to assume with Haase that Mimicry always arose in the female and was later acquired by the male. Both sexes of the third section of swallow-tails (Cosmodesmus) mimic Pharmacophagus in America, far more per- fectly than do the females of Papilio. But this is not due to Cosmodesmus presenting us with a later stage of the history begun in Papilio; for in Africa Cosmodesmus is still mimetic (of Danainae) in both sexes although the resemblances attained are imperfect, while many African species of Papilio have non-mimetic males with beautifully mimetic females. The explanation is probably to be sought in the fact that the females of Papilio are more variable and more often tend to become dimorphic than those of Cosmodesmus, while the latter group has more often happened to possess a sufficient foundation for the origin of the resemblance, in patterns which, from the start, were common to male and female. (5) In very variable species with sexes alike, Mimicry can be rapidly evolved in both sexes out of very small beginnings. Thus the reddish marks which are common in many individuals of Limenitis arthemis were almost certainly the starting-point for the evolution of the beautifully mimetic ZL. archippus. Nevertheless in such 138 THE VALUE OF COLOUR cases, although there is no reason to suspect any greater variability, the female is commonly a somewhat better mimic than the male and often a very much better mimic. Wallace’s principle seems here to supply the obvious in- terpretation ; but it is to be noted that the evo- lution of Mimicry is taking place in colours that are associated with sex. Otherwise, it is impos- sible to explain the fact that the more perfect Mimicry attained by one sex is not immediately transferred to the other. (6) When the difference between the patterns of model and presumed ancestor of mimic is very great, the female is often alone mimetic ; when the difference is comparatively small, both sexes are commonly mimetic. The Nymphaline genus Hypolimnas is a good example. In Hypolimnas itself the females mimic Danainae with patterns very different from those preserved by the non- mimetic males: in the sub-genus Evuralia, both sexes resemble the black and white Ethiopian Danaines with patterns not very dissimilar from that which we infer to have existed in the non- mimetic ancestor. (7) Although a melanic form or other large variation may be of the utmost importance in facilitating the start of a mimetic likeness, it is impossible to explain the evolution of any detailed resemblance in this manner. And even the large colour variation itself may well be the expression of a minute and ‘continuous’ change CONCLUSIONS ON MIMICRY AND SEX 139 in the chemical and physical constitution of pig- ments. (8) Female Mimicry is not by any means always a question of colour and pattern alone. Thus, the mimetic females of some Papilionidae lose the ‘tails’ which are retained by the non-mimetic males (e. g. P. dardanus = merope), and the females of the tropical American Nymphaline genus Evesia and Pierine genus Dismorphia and its allies, are not only better mimics in colour and pattern but also in shape of the wings. SEXUAL SELECTION (EPIGAMIC CHARACTERS) We do not know the date at which the idea of Sexual Selection arose in Darwin’s mind, but it was probably not many years after the ‘sudden flash of insight’ which, in October, 1838, gave to him the theory of Natural Selection. An excel- lent account of Sexual Selection occupies the concluding paragraph of Part I of Darwin’s Section of the Joint Essay on Natural Selection, read July 1, 1858, before the Linnean Society.! The principles are so clearly and sufficiently stated in these brief sentences that it is appro- priate to quote the whole : ‘Besides this natural means of selection, by which those individuals are preserved, whether in their egg, or larval, or mature state, which are best adapted to the place they fill in nature, there is a second agency at work in most unisexual animals, tending to produce the same effect, namely, the struggle of the males for the females. These struggles are 1 Journ. Proc. Linn. Soc., iii. 1859, 50. 140 THE VALUE OF COLOUR generally decided by the law of battle, but in the case of birds, apparently, by the charms of their song, by their beauty or their power of courtship, as in the dancing rock- thrush of Guiana. The most vigorous and healthy males, implying perfect adaptation, must generally gain the victory in their contests. This kind of selection, however, is less rigorous than the other; it does not require the death of the less successful, but gives to them fewer descendants. The struggle falls, moreover, at a time of year when food is generally abundant, and perhaps the effect chiefly produced would be the modification of the secondary sexual characters, which are not related to the power of obtaining food, or to defence from enemies, but to fighting with or rivalling other males. The result of this struggle amongst the males may be compared in some respects to that produced by those agriculturists who pay less attention to the careful selection of all their young animals, and more to the occasional use of a choice mate.’ A full exposition of Sexual Selection appeared in the Descent of Man in 1871, and in the greatly augmented second edition, in 1874. It has been remarked that the two subjects, The Descent of Man and Selection in Relation to Sex, seem to fuse somewhat imperfectly into the single work of which they form the title. The reason for their association is clearly shown in a letter to Wallace, dated May 28, 1864: ‘... I suspect that a sort of sexual selection has been the most powerful means of changing the races of man.’! Darwin, as we know from his Autobiography,? was always greatly interested in this hypothesis, and it has been shown in the preceding pages that he was inclined to look favourably upon it 1 More Letters, ii. 33. 2 Life and Letters, i, 94. DARWIN AND SEXUAL SELECTION 141 as an interpretation of many appearances usually explained by Natural Selection. Hence Sexual Selection, incidentally discussed in other sections of the present essay, need not be considered at any length, in the section specially allotted to it. Although so interested in the subject and not- withstanding his conviction that the hypothesis was sound, Darwin was quite aware that it was probably the most vulnerable part of the Origin. Thus he wrote to H. W. Bates, April 4, 1861 :— ‘If I had to cut up myself in a review I would have [worried ?] and quizzed sexual selection; therefore, though I am fully convinced that it is largely true, you may imagine how pleased I am at what you say on your belief.’ * The existence of sound-producing organs in the males of insects was, Darwin considered, the strongest evidence in favour of the operation of Sexual Selection in this group.? Such a con- clusion has received strong support in recent years by the numerous careful observations of Dr. F. A. Dixey* and Dr. G. B. Longstaff* on the scents of male butterflies. The experience of these naturalists abundantly confirms and ex- tends the account given by Fritz Miiller* of the scents of certain Brazilian butterflies. It is a remarkable fact that the apparently epigamic scents of male butterflies should be pleasing to 1 More Letters, i. 183. 2 Life and Letters, iii. 94, 138. 3 Proc. Ent. Soc, Lond., 1904, lvi.; 1905, xxxvii., liv. ; 1906, ii. * Proc. Ent. Soc. Lond., 1905, xxxv.; Trans. Ent, Soc. Lond., 1905, 136; 1908, 607. 5 Jen. Zeit., xi., 1877, 99; Trans. Ent. Soc. Lond., 1878, 211. 142 THE VALUE OF COLOUR man while the apparently aposematic scents in both sexes of species with warning colours should be displeasing to him. But the former is far more surprising than the latter. It is not per- haps astonishing that a scent which is ex hypothesi unpleasant to an insect-eating Vertebrate should be displeasing to the human sense; but it is certainly wonderful that an odour which is ex hypothesi agreeable to a female butterfly should also be agreeable to man. Entirely new light upon the seasonal appear- ance of epigamic characters is shed by the recent researches of C. W. Beebe,! who caused the scarlet tanager (Pivanga erythromelas) and the bobolink (Dolichonyx oryzivorus) to retain their breeding plumage through the whole year by means of fattening food, dim illumination and reduced activity. Gradual restoration to the light and the addition of meal-worms to the diet invariably brought back the spring song, even in the middle of winter. A sudden alteration of temperature, either higher or lower, caused the birds nearly to stop feeding, and one tanager lost weight rapidly and in two weeks moulted into the olivegreen winter plumage. After a year, and at the beginning of the normal breeding season, ‘individual tanagers and bobolinks were gradually brought under normal conditions and activities,’ and in every case moulted from nuptial plumage to nuptial plumage. ‘The dull colors of 1 The American Naturalist, xlii. No. 493, Jan. 1908, 34. CONTROL OF NUPTIAL PLUMAGE 143 the winter season had been skipped.’ The author justly claims to have established ‘that the se- quence of plumage in these birds is not in any way predestined through inheritance...... , but that it may be interrupted by certain factors in the environmental complex’. Mr. Beebe’s deeply interesting investigations on birds prove that external stimulus may be as necessary for the production of the tints displayed in courtship as for other colours that are character- istic of the species (p. 110). Birds may thus exhibit the individual susceptibility to environment so well known in numbers of insect larvae and pupae (p. 109). Although certain naturalists, especially the students of plant oecology,’ consider that re- sults of this kind are opposed to a Darwinian interpretation, it is perfectly clear that ‘the changes so produced must, like any other varia- tions, pass through the ordeal of the survival of the fittest’? And when each possible response is appropriate to the special environment which provides the stimulus, it is obvious that, so far from witnessing the elimination of Natural Selec- tion, we are in presence of its highest manifesta- tion. 1See J. M. Coulter in Fifty Years of Darwinism, New York, 1909, 61-3. 2 Hditors of More Letters, i. 214 n, 1. VI MIMICRY IN THE BUTTERFLIES OF NORTH AMERICA Written from the notes of the Anniversary Address de- livered to the Entomological Society of America, Baltimore, Thursday, December 31, 1908. INTRODUCTORY Wiruin a few weeks of the hundredth anni- versary of Darwin’s birth, and nearly midway between the fiftieth anniversaries of the publica- tion of Natural Selection on July 1 last and the Origin of Species on Nov. 24 next, it seemed to me specially appropriate to select for this address a subject that is closely associated with Darwinian teachings. Although he did not publish it during his lifetime, we now know from his correspond: ence that Darwin independently originated the interpretation of Mimicry which was afterwards suggested by H. W. Bates.1 Its development in the mind of the naturalist of the Amazons and the rival theory afterwards suggested by Fritz Miller, were both of them the direct outcome, in Bates’s case the very speedy outcome, of the Origin. The deep interest which Darwin took in the 1 See pp. 123-4. MIMICRY AND EVOLUTION 145 hypotheses of both naturalists is proved by many a letter in his published correspondence. All this forms a peculiarly fascinating chapter of ancient history,—nevertheless ancient history ; but if we desire to choose a subject because of the light it can throw to-day and is certain to throw to-morrow upon evolution and its causes, there is no study which for promise as well as performance can be set on a higher level than Mimicry. In the course of the following address the word ‘ Mimicry’ will be used with the restricted mean- ing attached to it by A. R. Wallace. It will be applied solely to the superficial resemblances between animals, and not to their likeness to vegetable or mineral surroundings for the purpose of concealment. The study of Mimicry is of the highest value in relation to both evolution itself and the motive causes of evolution. Apart from all question of the means by which Mimicry has been produced, it will be generally admitted that the mimetic species has in some way evolved a superficial resemblance to the pattern of one or more species, more or less remote from it in the scale of classification. Looking on the changes by which the resem- blance has been produced as a piece of evolu- tionary history, and, as I have said, disregarding for the moment their causes, we have one of the 1 See pp. 123-9. L 146 MIMICRY IN N. AMERICAN BUTTERFLIES very simplest and sharpest pictures of organic transformation presented for our investigation. An effect—generally a strongly marked and con- spicuous effect—has been brought about in those elements which make up the superficial appear- ance of a species, and this important change is manifestly in the direction of only a minute fraction of the infinitely complex organic environ- ment, viz. that fraction contributed by the super- ficial appearance of one or more very different species, commonly indeed of but a single one. When, as in North America, a recent invader becomes the model determining the direction of evolution in some constituent of the ancient butterfly fauna, the case becomes especially striking. The effects produced on the mimic are generally sharper and more distinct than those seen in the concealing resemblances to bark, lichen, earth, &c.,—the difference corresponding to the more definite and individual appearance usually presented by the pattern of the model as compared with such elements in the vegetable and mineral surroundings. There are also other important differences. The models of Mimicry are generally more restricted in their range, and differ more widely in different areas and in different parts of the same area than the models of cryptic resemblance. Differences between the local forms of the same model imply that the mimicked species has itself been subject to rapid MIMETIC AND CRYPTIC COLOURS 147 change, while the models of cryptic resemblance appear by comparison to be stereotyped and permanent. Furthermore the models as well as their mimics within the same area are liable to changes of distribution, whereas the models of cryptic resemblance are as a rule comparatively fixed. A mimetic species may often be found passing into an area where its model exists in a different form or does not exist at all, and highly instructive conclusions may be drawn from the study of the corresponding changes. In accordance with the facts briefly summarized in the above statements, we find that better and more numerous examples of rapid recent change are to be found in mimetic patterns than in those which promote concealment. Not only is this evident when we trace the geographical changes of model and mimic over a wide continuous area, but in many cases the same genus includes both mimetic and non-mimetic species, the latter enabling us to infer with more or less certainty the ancestral appearance of the former. The history thus unravelled may often be further confirmed by a study of the non-mimetic males of mimetic females. Many naturalists at the present day incline to return to the old belief that the history of evolu- tion has been ‘discontinuous’, proceeding by ‘mutations’ or large and definite steps of change. The comprehensive and detailed study of Mimicry as a piece of biological history certainly provides L2 148 MIMICRY IN N. AMERICAN BUTTERFLIES one of the best and safest means—perhaps the very best—of forming a judgement between this revived opinion and Darwin’s conclusion that, although the rate of transformation varied greatly and might slow down to nothing for long periods, the steps of change were small, forming a gradual and ‘ continuous ’ transition between the successive forms in the same evolutionary history.! The study of the causes of Mimicry is more difficult than that of the history of Mimicry, the conclusions far less certain. Nevertheless the evidence at present available yields much support to the theory of Natural Selection as the motive cause of evolution. The facts certainly do not point to any other interpretation. They negative the conclusion that mimetic resemblances have been produced by the direct action of external forces (Hypothesis of External Causes) or by variation unguided by selection (Hypothesis of In- ternal Causes). Nor do they support Fritz Miller’s earlier and daring speculation (see pp. 127-8) that female preferences were influenced by the sight of the patterns displayed by the models (Hypothesis of Sexual Selection). The only hypotheses which are in any way consistent with the body of facts, considered as a whole, are those which assume that the resemblances in question have been built up by the selection of variations beneficial in the struggle for life. In its concentration on a minute fraction of the 1 See pp. 42-51; also Appendix B, p. 254. SUGGESTED CAUSES OF MIMICRY 149 total organism as well as in the rapidity of the results achieved, the operation of Natural Selection in the production of Mimicry is more than ordi- narily akin to the methods of Artificial Selection. Indeed a very fascinating and promising line of investigation in a suitable locality would be the attempt to initiate or improve a mimetic likeness by means of Artificial Selection. Mimetic resemblances are of two kinds, re- spectively interpreted by two well-known hypo- theses, both based on the theory of Natural Selection. 1, Mimicry as interpreted by H. W. Bates is an advantageous deceptive resemblance borne by palatable or harmless species (the mimics) to others that are unpalatable or otherwise specially defended (the models’. Such resemblance will be spoken of as Batesian Mimicry, the examples as Batesian mimics, the interpretation as the Batesian Hypothesis. 2. The resemblances between specially defended species themselves, although well known to Bates, were not explained by his hypothesis as he con- ceived it. He suggested that they were an expression of the common results produced by forces common to the environment of the species in question. Such likenesses! were subsequently interpreted by Fritz Miller as the advantageous adoption of a common advertisement by specially 1 It is probable that these were the examples which Fritz Miiller had previously sought to explain by the theory of Sexual Selection. See pp. 127-8 of the present volume. 150 MIMICRY IN N. AMERICAN BUTTERFLIES defended species, whereby the loss of life incurred during the education of young inexperienced enemies was contributed between the similar forms, instead of by each species independently as would have been the case if they had been dissimilar, and possessed patterns requiring each a separate education. Such resemblance will be spoken of as Millerian Mimicry, the examples as Miillerian mimics, the interpretation as the Miil- lerian Hypothesis. SPECIAL ADVANTAGES OF THE NORTH AMERICAN BUTTERFLY FAUNA FOR THE STUDY OF MIMICRY The butterfly fauna of North America affords probably the best field in which to begin the study of Mimicry,—a subject which has been shown to possess the most profound significance in relation to the deepest problems by which the naturalist is confronted. The examples are sharp and striking, but not too numerous, and the inquiry can be approached without the confusion and excessive strain on the memory which must inevitably at first beset the student of Mimicry in the tropics. But outside the tropics it is also the best field for this study, as will be shown below. The western section of the Palaearctic Region is sharply cut off by the Sahara from the Ethiopian, and its ‘few examples of Mimicry are not such as would be likely to awaken the interest and enthusiasm of the beginner. The eastern Palae- SPECIAL ADVANTAGES OF N. AMERICA 151 arctic section suffers from the opposite defect. Separated by imperfect barriers from the Oriental Region, its butterfly fauna is complicated by much invasion of specially protected species from the tropics, and the examples of Mimicry are too numerous and too little known. North America occupies a position conveniently intermediate between the two sections of the Palaearctic por- tion of the circumpolar land-belt. It has been invaded by models from the eastern tropics of the Old World and also probably from the tropics of the New; but the species are few and their effects upon the indigenous butterflies sharp and distinct. The Mimicry itself affords striking and remarkable evidence of the lines of migration followed by some of the intruding models. The ancestral forms from which the mimics were derived, have nearly always persisted, and enable us to unravel the history of the change, with exceptional clearness. The examples bear in a most interesting manner upon the two great hypotheses associated respectively with the names of H. W. Bates and Fritz Miller. Although the butterfly fauna is as well known as that of any part of the world, the mimetic resemblances supply material for a large amount of much- needed original investigation, inviting the atten- tion of American naturalists in almost every locality. 152 MIMICRY IN N. AMERICAN BUTTERFLIES THE DANAINE MODELS OF NORTH AMERICA, AND THEIR RELATIONSHIP TO THE SOUTH AMERICAN AND OLD WORLD DANAINAE! The Danainae are the most important and most extensively mimicked of all specially protected butterflies in the Old World tropics. The Acraei- nae, so abundant in Africa, are also greatly mimicked, but to a far less extent than the com- paratively few species of Danainae found in the same Region, —all belonging to the section Danaini. The Ethiopian Acraeas in fact supply several mimics of the Danaines, but no example of the opposite relationship is known. In the tropical East, the Acraeinae are poorly represented, while the Danainae (Danaini, Euploeini, Hestia, Hama- dryas) are dominant in numbers as well as in the power of influencing the patterns of other butter- fly groups. In both Africa and the East, Miul- 1 The subject of the address from this point onwards is treated in considerable detail in the author’s memoir, Mimetic North American species of the Genus Limenitis (s.l.) and their models, in Trans. Ent. Soc. Lond., 1908, 447-88. Dr. Jordan’s later con- clusions as to the affinities of Danaida plexippus, added to the memoir in a terminal note (488) and somewhat at variance with his earlier conclusions quoted in the text, are here adopted throughout. A broader and less detailed treatment is followed in this address, special attention being directed to the numerous points on which further observations are required. Where no other authority is mentioned I have followed the synonymy and geographical distribution of Scudder’s great work, Butterflies of the Eastern United States and Canada, and, for the Papilionidae, Rothschild and Jordan's fine monograph (Nov. Zool., xiii, 1906, 411-752). I have not, however, followed Scudder in the general use of Basilarchia as a generic name, because I think that the whole group of Limenitis, in its widest acceptation, requires revision, and that until this has been accomplished it is inexpedient to adopt the terminology proposed for a portion of it. THE WORLD MODELS FOR MIMICRY 158 lerian Mimicry is evident between the different genera and sections of the specially protected groups themselves. In the richest and most remarkable butterfly fauna in the world, that of South America, the dominant specially protected group is composed of the Ithomiinae, allied to the Danainae, and called by Bates ‘ Danaoid Heliconidae’. Next in importance come the Heliconinae, allied to the Acraeinae, and called by Bates ‘ Acraeoid Heli- conidae ’. Both of these are extensively mimicked, especially the Ithomiinae : in fact it was the close and obvious Mimicry of these by certain species of the Heliconinae that puzzled Bates and ultimately received an interpretation in the Millerian Hy- pothesis. In addition to the above, this rich and varied Region contains numerous true Acraeinae, mimicked considerably, and a small number of true Danaine species. These latter, which are of extreme interest, fall into two groups. One of them, the Lycoraeini, containing the two genera Lycorea and Ituna, is confined to South America, and bears evident traces of long residence in the Region. The whole of the species are mimetic of various dominant Ithomiine genera, while at the same time some of them appear also to act as models for other butterflies, in a single case (Ituna phenarete) even for one of the rarer species (Eutresis imitatrix) belonging to the Ithomiinae themselves. It was the resemblance between the Lycoraeine genus tuna and the Ithomiine 154 MIMICRY IN N. AMERICAN BUTTERFLIES genus Thyridia that led Fritz Miiller to his hypothesis, and formed the title of the paper in which he first expounded it. The Lycoraeini are widely different from any of the Old World Danainae and are sometimes separated from them as a distinct sub-family. The second group of Danaines, found in North America as well as South, belongs to the Old World section Danaini, and is in every respect strongly contrasted with the Lycoraeini. Its species, divided into two genera Anosia and Tusitia by Moore, are not known to enter into mimetic relations with any of the other butterflies of this southern Region.! Furthermore, they not only belong to a dominant Old World section of the Danaines, but are even closely allied to particular species within it. It is probable that there are only two well-marked species of Danaini on the American Continent, and that the various forms encountered over this vast area are the geographical races or sub-species of these two. In north temperate America they are the well-known models for mimicry,—Anosia plexippus extending far into Canada, and Tasitia berenice and its form strigosa not ranging beyond the southern States. In 1897, at the Detroit meeting of the American Association for the Advancement of Science, I suggested * that the Mimicry of Anosia plexippus 1 It is possible, however, that there are incipient resemblances to Anosia in certain 8, American Acraeinae. * Proc. Am. Assoc, Adv. Sci., 1897, xlvi. 244. HISTORY INFERRED FROM MIMICRY 155 by Limenitis (Basilarchia) archippus was evidence that the model had long resided in North America, and that we might on this ground alone, even if we had not abundant positive evidence of its gradually increasing spread in the Old World during the past half-century, infer that Anosia had reached Fiji, Australia, Hong-Kong, &c., in comparatively recent times. This conclusion can hardly be doubted, and the argument might have been extended to enable us to infer the ancestral line of migration by which North America itself had been reached by this form. But in 1897 I followed what appeared to be the general view, that, in the New World, the original stream of Danaine invasion had run from the American tropics northward,! nor did I observe that the evidence based on the growth of mimetic resem- blance warranted the interesting conclusion that its flow had taken the opposite direction, and that the south had been peopled by way of the north. Accepting this conclusion the question arises: Whence came the Danaini of North America? The answer requires a somewhat careful comparison between the New and Old World butterflies of this group. Among the commonest of the Old World Danaini, are certain species with tawny colouring, a black border, and black white-barred apex to the fore wing. The under surface is even more 1 Verhandl. d. V. Internat. Zool. Congr. z. Berlin, 1901, Jena, 1902, 171. See also Essays on Evolution (1908), 274: also errata. 156 MIMICRY IN N. AMERICAN BUTTERFLIES conspicuous than the upper, being brighter in colour and the black border marked with white in a more striking manner. In one set of Oriental species, placed by Moore in his genus Salatura, the veins are heavily marked with black on both surfaces, conferring a very characteristic appearance, especially upon the hind wing. The other set of species in which the veins are com- paratively inconspicuous is placed by Moore in Limnas, including L. chrysippus, perhaps the commonest butterfly in the world, ranging from the Cape to Hong-Kong and perhaps to Japan. It is clear, however, that Africa is its ancestral home; for it is there mimicked far more exten- sively than in any other country.!' In the Malay Archipelago, both Salatura and Limnas are repre- sented by various forms, and in some of these the tawny colouring becomes much darkened. This tendency appears to be more frequent in LTimnas, and when both forms have darkened in the same island (e.g. Java) it is probable that Limnas has acted as the model for Salatura. There is a close general resemblance in colouring and pattern between Salatuwra of the Old World and Anosia of the New, as also between Limnas of the Old World and Tasitia of the New. Furthermore the two New World species differ from each other in the same points as do those of the Old. The dark, white-barred apex of the fore wing, so conspicuous in the Old World forms, is less 1 Proc. Am. Assoc. Adv. Sci., 1. ¢., 244. NEW AND OLD WORLD DANAIDAS 157 emphasized in those of the New, being especially evanescent in Tasitia where, however, traces of the white markings remain distinct. It is sig- nificant, however, that the black and white apex is also lost in one of the forms of L. chrysippus, viz. the variety dorippus (= klugii), abundant in many parts of Africa and also extending by way of Aden and the west coast of India as far as Ceylon. There is, in fact, much resemblance between the pattern of dorippus and such a form of Tasitia as berenice, the likeness being especially apparent in the indications of the former presence of the white apical bar. In the forms of TZasitia, as in some of Limnas, the ground-colour becomes darker and richer—a development especially well seen in J. berenice of Florida. Thus the two chief points in which the pattern of Tasitia differs from that of typical L. chrysippus, viz. the darker, richer ground-colour and the evanescent apical markings, are both presented by abundant Old World forms of the latter species. The superficial resemblances between these Old and New World Danaines are precise and often extend to minute details. Thus the scent-pouch on the hind wings of the male, best seen from the under surface, is similar in Salatura and Anosia, while the resem- blance between Limnas and Tasitia in this respect is even more striking. The resemblances above described suggested the investigation and comparison of structural charac- ters in order still further to test the relationship 158 MIMICRY IN N. AMERICAN BUTTERFLIES between these Old and New World Danaines, and also the validity of the genera created by Moore.! Such a comparison had already been partially made by Rothschild and Jordan, who in 1903 published the conclusion that Limnas and Tasitia cannot be generically separated.? I therefore wrote to my friend Dr. Jordan, asking if he would kindly extend his survey over all the four so-called genera. He found that in Salatura genutia and Anosia plexippus, having larvae with two pairs of fila- ments,* the male genitalia are of the same type ; while in Limnas chrysippus and Tasitia berenice, having larvae with three pairs of filaments, these genitalia are of a second type. The final opinion of this distinguished authority on the relationships between the Rhopalocera, was given in the fol- lowing words * :— ‘It appears to be certain that Anosia plexippus does not stand apart from the others. Therefore, if Tasitia berenice, Limnas chrysippus and Salatura genutia are placed in one 1 Proc. Zool. Soc. Lond., 1883, 201. 2 Nov. Zool. vol. x, Dec., 1903, 502, * Dr. Jordan was at first inclined to think that Anosia plexippus should be separated generically, basing his conclusion in part on the larval characters (Trans. Ent. Soc. Lond., 1908, 450). A more extended review of the Tring material pointed in the opposite direction, and Dr. Jordan wrote on December 10, 1908, as follows:— ‘T find from our specimens Had preserved larvae] that— (1) in Euploea (in the wide sense) there are 4 pairs of filaments, or three (the 3rd being absent), or two (the 8rd and 4th being absent). 2) In Danaidae, incl. of Anosia & Limnas, there are 3 pairs (the 3rd of the 4 pairs of Euploea being absent), or 2 pairs (the 2nd and 8rd being absent). I find that, for instance, genutia and purpurata have 2 pairs only, like plewippus. The larva therefore does not furnish any argument for separating plexippus as a enus.’ 4 In a letter to the author, dated December 15, 1908. ALL DANAIDAS CLOSELY RELATED 159 genus,’ plexippus also must be included. I do not think you need hesitate thus to simplify the classification of these insects.’ I have no hesitation in accepting this advice, and in fusing all the four genera created by Moore into the single genus Danaida. Within this genus it has been made evident that the group of forms ranged around Danaida plexippus is the New World representative and close ally of the group of D. genutia; while that of D. berenice is similarly representative of the group of D. chrysippus. It is interesting to note that both the American Danaidas have become much larger than the corresponding Old World species, and that the most northern forms are larger than the southern in both hemispheres—the probable result of a slower metamorphosis in a more temperate climate. EVIDENCE THAT DANAIDA IS AN OLD WORLD GENUS THAT HAS INVADED THE NEW The suggestion might perhaps be made that the New World forms of Danaida are the more ancestral, and that those of the Old World have been. derived from them by migration westward. There is no reason for concluding that the Danaidas of either geographical area possess a more primitive structure than those of the other ; we are therefore driven to consult other lines of 1 Dr, Jordan's opinion that these three genera should be united is quoted in Trans. Ent. Soc. Lond., 1908, 450. 160 MIMICRY IN N. AMERICAN BUTTERFLIES evidence. The following comparisons clearly indi- cate that Danaida is an Old World genus which has invaded America at no very remote period: (1) the far larger number of the Old World forms and the greater degree of specialization by which some of them are distinguished ; (2) the place of Danaida as one out of a number of nearly related genera making up the Danaini, a large and dominant Old World group, per contra its isolated position in the New World; (8) The highly developed and complex mimetic relationships of the Old World Danaidas, This last statement requires some expansion and exemplification. Allusion has already been made to the resemblances which have grown up between different species of Danaida in the same island,—resemblances in which the forms of chrysippus appear to act as models. Even more striking is the mimetic approach of certain Old World Danaidas to species of the other dominant Oriental section of the Danainae—the Euploeini. Thus in the Solomons, Danaida (Salatura) insolata is a beautiful mimic of the dark white-margined Euploea brenchleyi, while in the same islands, Danaida (Salatura) decipiens mimics the dark, white-spotted Huploea asyllus.1 Finally, and most convincing as evidence of long residence, are the numbers of mimics which in the Old World have taken on the superficial appearance of species of 1 See J. C. Moulton in Trans. Ent. Soc. Lond., 1908, 608, 604: Pl, XXXIV, figs. 5, 10. MIMICRY OF OLD WORLD DANAIDAS 161 Danaida., In addition to the extraordinary degree to which the Mimicry of D. chrysippus is carried in Africa, it is mimicked in the Oriental Region by the females of Hypolimnas misippus and of Argynnis niphe, and by the males of certain species of Cethosia. Danaida genutia and the forms related to it are also mimicked by male Cethosias and extensively by the females of species of Elymniinae, while incipient Mimicry is seen in the males of some of them. With the exception of Hypolimnas misippus, common to both Regions, the Oriental mimics of Danaida do not approach the degree of resemblance attained by the best African mimics of D. chrysippus. It has already been pointed out that the Oriental mimics of this genus are far less numerous than the African. On the other hand, it is a curious fact that the only North American mimic of D. plexippus,—Limenitis (Basilarchia) archippus—reaches a far higher degree of resemblance than that attained by any of the characteristically Oriental mimics of Danaida. The evidence as a whole enables us to decide that Danaida is an Old World genus and a com- paratively recent intruder into America, while the perfection of the likeness attained by an indigenous American mimic proves that, under favourable circumstances, such resemblances may be rapidly produced. I do not, of course, mean to imply that the transformation was in any way sudden, or by other than minute transitional M 162 MIMICRY IN N. AMERICAN BUTTERFLIES steps. The evidence for this conclusion will be clearer when some of these steps have been described in detail (see pp. 164-8). THE LINE OF MIGRATION BY WHICH DANAIDA ORIGINALLY ENTERED AMERICA There can be little doubt that D. plexippus invaded America by way of the north, probably following the line of the Aleutian Islands. In North America it possesses an astonishing distri- bution for a member of so tropical a group, ranging immensely further north than any other Danaine in the world. Furthermore, D. genutia, the probable representative of its Old World ancestor, extends far beyond the tropics into Western and Central China. A study of the distribution of the Asclepiad food-plants on the eastern coast of Asia might perhaps throw light on the problem. JD. plexippus was certainly the earlier of the two invaders of the New World. This is clearly shown by the extent of its own modification no less than by the changes it has itself produced. Its immense size, the shape of the hind-wing cell, and the form of the fore wings indicate that it is far more widely separated than is D. berenice from the nearest Old World species. It has furthermore been resident in North America long enough to effect profound changes in the pattern of an indigenous Nymphaline butterfly, rendering it an admirable mimic; whereas D, berenice, and probably its form strigosa INVASION FROM THE NORTH 163 also, have only effected comparatively slight modifications in the mimetic pattern already produced under the influence of plexippus (see pp. 168-72), It is impossible to feel equal confidence in suggesting the line by which the later invasion of the more tropical D. berenice took. place ; but it is on the whole probable that it too came by way of the north during some temporary period of warmth. It is tolerably certain that it did not invade North America from the south. For although D. berenice and strigosa have produced—as is shown above—far less change in the indigenous N. American fauna than plexippus, they have still caused distinct and perfectly effective modifications in a single species; whereas in South America their representatives have not been shown to have had any effect at all. It is probable that both the American Danaidas as they pressed southward were ‘held up’ for a considerable time at the northern borders of the Neotropical Region, unable at first to penetrate that crowded area. Finally they burst their way through and are now abundant throughout all the warmer parts of the Region, the forms of plexippus extending further into the temperate south, just as in the Northern Hemisphere they range further north than those of berenice. We are made to realize the recent date of the invasion of South America when we remember that nowhere else in the world do Danaine butterflies of equal abundance ‘range M2 164 MIMICRY IN N. AMERICAN BUTTERFLIES through a crowded area without producing any effect on any member of the Lepidopterous fauna, or without themselves being affected thereby.’! Abundant wide-ranging Danaines in the Old World, even when much smaller and with a less marked appearance, invariably produce some effect, and often themselves exhibit Miillerian resemblances. THE EVOLUTION OF LIMENITIS (BASILARCHIA) ARCHIPPUS AS A MIMIC OF THE INVADING DANAIDA PLEXIPPUS It has already been mentioned that a single species, undergoing corresponding modifications, provides a mimic for each of the three Danaine models (including strigosa). We will first con- sider the well-known beautiful mimic of D. plez- tppus; for it undoubtedly arose earlier than the others. The abundant Limenitis or Basilarchia archippus is closely related to the Palaearctic species of Limenitis, a group which includes the well-known British ‘White Admiral’ (L. sybilla). The ex- ample is unusually instructive, because the non- mimetic ancestor of the mimic is still very abundant in Canada and the north-eastern States, and we thus possess the material for reconstruct- ing the history by which the one form originated from the other. We know that this ancestor, Limenitis arthemis, has persisted almost unchanged, 1 Trans. Ent. Soc. Lond. (1908), 452. NON-MIMETIC PARENT OF MIMIC 165 because of the resemblance between its pattern and that of other species of Limenitis (using the name in the broad sense) from all parts of the circumpolar land-belt, including North America itself. The difference between the pattern of the mimic and that of its non-mimetic parent is enormous—probably as great as that between any two butterflies in the world; but the steps by which the transition was effected were long ago suggested by S. H. Scudder,’ and have recently been worked out in considerable detail by the present writer.? L. arthemis exhibits the characteristic ‘ White Admiral’ pattern—possessing on the upper sur- face a dark ground-colour with a broad white band crossing both wings, and white markings within the apex of the fore wing. Reddish or orange spots between the white bands and the margin are found in the hind wings of many individuals, more rarely in the fore wings. These latter markings are of the utmost importance, for, as Scudder long ago pointed out (l.c., 714), they undoubtedly provided the foundation for the change into the mimetic archippus. A careful comparison between arthemis and archippus reveals the most conclusive evidence of selection. The one species has become changed into the other precisely as if an artist were to paint the pattern of archippus upon the wings 1 Butterflies of the Eastern United States and Canada, Cambridge, Mass. (1889), 278, 714. 2. Trans. Ent. Soc. Lond. (1908), 454-60. 166 MIMICRY IN N. AMERICAN BUTTERFLIES of arthemis, retaining unchanged every minute part of the old markings that could be worked into the new, and obliterating all the rest. Thus, extending in this direction and wiping out in that, the great transformation has been effected and one of the most beautiful mimics in the world produced. The evolution of the mimetic pattern on the under surface has involved an even more elabo- rate change than on the upper; but it is not necessary to repeat here the details which have been only recently fully described.! I will, how- ever, allude to the fate of the most conspicuous feature of arthemis, the broad white band crossing both wings. Save for the traces mentioned below, this marking has disappeared from both surfaces of the hind wing of archippus, but its black outer border is retained, and, cutting across the radi- ate pattern formed by the strongly blackened veins, detracts considerably from the mimetic resemblance.2- On the under surface distinct 1 Trans. Ent. Soc. Lond. (1908), 454-60. ? In the course of the address on December 81, 1908, I remarked that if we could revisit the earth in a few hundred years we might expect to find that this black line had disappeared from the hind wing, and the mimetic resemblance correspondingly heightened. Atthe conclusion, Mr. John H. Cook of Albany, N.Y., informed me that he had discovered near his home many individuals in which the black line was wanting from the upper surface. A few days later he very kindly sent me a record of his observations, of which an abstract is printed as a note at the end of this address (see pp. 211-12). The study of Mr. Cook's facts shows that near the city of Albany not only did the stripeless variety occur commonly (1 in 14', during the three seasons in which the observations were conducted, but also transitional forms with more or less broken stripes were far commoner than the normal archippus (18 to 1). The ANCESTRAL TRACES IN THE MIMIC 167 traces of the white band may commonly be seen along the inner edge of the persistent black border. So far as my experience goes these traces are only to be found on the upper surface in the form hulsti (Edw.). The modification of the same marking in the fore wing is more in- teresting. Here towards the costal margin the black outer border is much expanded, invading the white band and cutting off from two to four white spots from its outer part. While the rest of the band disappears except on the costa itself, these black-surrounded white spots now repre- sent the sub-apical pale-spotted black bar of the model. The new marking is larger and more conspicuous on the under surface, corresponding with the strong development of white on this surface of the model. The costal margin of the fore wing of the latter is streaked with long narrow white markings. In correspondence with this we find, commonly on the under surface, more rarely on the upper, that the extreme fact that entirely stripeless individuals were invariably males is contrary to the rule that mimetic resemblance tends to develop more rapidly and fully in the other sex. But in this species I have observed another point in which the female tends to be more ancestral than the male, viz. the more frequent and complete development of the white spot in the cell of the fore-wing upper surface (a2 common feature of Limenitis, although now generally absent from L. arthemis). Mr. Cook's observations show that a single marking—and one so simple that we might have expected it to act as a ‘unit character ’, so small a fraction of the pattern that we could hardly speak of its sudden disappearance as ‘discontinuous’ evolution —that even this behaves differently on the two surfaces of the wing, while the individuals from which it has disappeared are immensely outnumbered by those in which it is transitional. 168 MIMICRY IN N. AMERICAN BUTTERFLIES costal end of the white band is retained, often for the full breadth of the marking, forming a linear streak. I have dwelt upon the changes undergone by the white band as an example of the way in which the new markings have been carved out of the old. The changes in the elaborate marginal pattern would have been equally convincing as evidence for a gradual and ‘continuous’ trans- formation. THE MODIFICATION OF THE LIMENITIS MIMIC OF DANAIDA PLEXIPPUS INTO A MIMIC OF D. BERENICE IN FLORIDA Danaida plexippus occurs together with D. bere- nice in Florida, but the latter far outnumbers the former, and the modification of Limenitis archippus into the form floridensis, Strecker (= eros, Edw.) is probably entirely due to the predominance of one model over the other. Data for determining the exact proportions in various localities would be of high interest. There is no reason for believing that berenice is in any way more or less distasteful than plexippus, but its abundance makes it a more conspicuous feature in the environment. It is evident that the change has been of the kind expressed in the above heading ; for, as has been already implied on pp. 162-8, traces of the former Mimicry of plexippus persist in floridensis and tend to detract from the resemblance more NEW MIMIC EVOLVED FROM OLD 169 recently developed. This is especially the case with the conspicuously blackened veins of archip- pus, which are so important a feature in the like- ness to plexippus. These, although obscured by the general darkening, are still recognizable in Jloridensis, diminishing its resemblance to berenice on the upper surface of both wings and on the under surface of the fore wing. Inasmuch as the details have been recently published else- where,! I will only dwell on one further point in the resemblance of jfloridensis to berenice—and that because the extensive observation of large numbers of specimens is greatly needed. I spoke on pp. 166-7 of the persistent traces of the white band on the hind-wing under surface in many individuals of LZ. archippus. These are ancestral features, diminishing the mimetic resemblance to D. plexippus. But in D. berenice there are conspicuous white spots towards the centre of the hind-wing under surface, and these, at any rate upon the wing, would bear some resemblance to the ancestral spots of the Limenitis mimic. Now in my very limited experience of floridensis these spots were sometimes exceptionally deve- loped and, outlined with black on their inner edges, were certainly far more distinct and con- spicuous than in L. archippus. The appearances I witnessed suggested the possibility of the recall of a vanishing feature in consequence of ' Trans. Ent. Soc. Lond. (1908), 460, 461. See also Scudder, loc, 718. 170 MIMICRY IN N. AMERICAN BUTTERFLIES selection based on a likeness to certain white spots present in the new model (berenice) but absent from the old (plexippus). But many hundreds of specimens from different localities scattered over the total area of distribution re- quire to be examined from this point of view. An even more interesting inquiry would be to trace the range of the floridensis form northward and determine the relationship of its limits to the zone in which berenice becomes scarce and disappears, and above all to ascertain whether Jloridensis on the borders of its range interbreeds with archippus and how far transitional varieties occur. Interbreeding between the two forms, if possible, would be of extraordinary interest. It is also of importance to ascertain precisely how far the one form penetrates the area of the other. Scudder indeed states that floridensis ranges into the Mississippi Valley and Dakota, far beyond the limits of Danaida berenice. It would be deeply interesting to make an exact comparison between such specimens and those from Florida, and also to ascertain the proportion which they bear to typical archippus. By far the most important feature in the evolution of Jloridensis is the general darkening of the ground- colour, and the material for such a transformation certainly exists freely in archippus, for the shade of brown varies immensely and may often be seen of as dark a tint as in floridensis, but not in my experience of precisely the same shade. INVESTIGATIONS REQUIRED 171 The proportion of such dark forms in various parts of the immense range of archippus would be another interesting inquiry. THE MODIFICATION OF THE LIMENITIS MIMIC OF DANAIDA PLEXIPPUS INTO A MIMIC OF THE STRIGOSA FORM OF D. BERENICE IN ARIZONA The differences between DL. archippus and the form hulsti (Edw.) are more striking than those which distinguish jfloridensis from the former. The upper surface of the hind wing of hulsti retains or more probably has recalled distinct traces of the white band, although the black stripe is evanescent. It is probable that, upon the wing, these vestigial white markings produce a general likeness to the pale-streaked hind-wing upper surface of strigosa. Other points in which hulsti differs from archippus and approaches stri- gosa are the reduction of black and the general appearance of the white spots in the subapical region of the fore wing, and the dull tint of the ground-colour. I have had hardly any experi- ence of this interesting form and owe the above details to Dr. W. J. Holland’s figure and descrip- tion. It is obvious that all the investigations suggested in the case of floridensis are, mutatis matandis, equally available and equally important in the form hulsti. 1 Butterfly Book, 84, 185, Pl. vii. f.5. Dr. Holland fully recog- nizes the mimetic significance of the pattern and colouring of hulsti. 172 MIMICRY IN N. AMERICAN BUTTERFLIES The geographical distribution of halsti strongly supports the conclusion that it was derived from archippus and not immediately from an arthemis-like ancestor. I have not yet had the opportunity of ascertaining whether this hypothesis is supported by evidence derived from a careful study of the pattern. It is deeply interesting to observe that the same Limenitis arthemis-like species, from which archip- pus, floridensis and hulsti—mimics respectively of the three Danaidas, plexippus, berenice and strigosa—have been directly or indirectly evolved, has also given rise to L. astyanax (ursula), the mimic of a Papilionine model. Evidence in favour of the comparatively recent origin of these mimicking forms is to be found in the well-supported facts which indicate that astyanax still interbreeds with arthemis along their geographical overlap, and that it may even occasionally pair with the sister species archippus.? The earlier stages of archippus and astyanaz are, according to Scudder (l.c., 254, 255), with difficulty distinguished from those of arthemis, but astyanax presents the closer likeness of the two; a fact which, together with those referred to in the last paragraph, points to the conclusion that it arose even more recently than archippus. The further consideration of astyanax is best deferred until some account has been given of the 1 Scudder, 1. c., 283,289. Trans. Ent. Soc. Lond. (1908), 473, 474- RECENT ORIGIN OF MIMICS 173 Papilionine models, and until certain general conclusions have been discussed in the following section. BEARING UPON THEORIES OF MIMICRY OF THE TRANSFORMATION WROUGHT BY THE INVADING DANAIDAS It has been shown that the Danaine models invaded America from the Old World tropics, probably following a northward route. Their patterns are but little changed in the new sur- roundings, and they still keep the characteristic appearance of Old World Danaidas. Furthermore, such changes as have taken place in the older invader, D. plexippus, during its residence in the New World, are also retained in those colonies which, during the past half-century, have been re-establishing themselves in the Old World. These facts support Darwin’s conclusion that the physico-chemical influences of soil, climate, &c., are of comparatively slight importance, a conclu- sion which made him feel ‘inclined to swear at the North Pole, and . . . to speak disrespectfully of the Equator ’. The mimics on the other hand are derived from characteristic and ancient inhabitants of the northern land-belt. If, as the followers of the theory of External Causes (see p, 148) maintain, species are the expression of the physical and 1 In a letter to Sir Charles Lyell, Oct. 11, 1859.—Life and Letters, ii. 212. 174 MIMICRY IN N. AMERICAN BUTTERFLIES chemical forces of the environment, then the Danaidas express the Old World tropics and the species of Limenitis the northern land-belt. We might expect on this theory that the Danaidas, when they invaded the northern zone, might come to resemble the Limenitis ; but the transformation that has actually occurred is entirely inconsistent with any such hypothesis. Although the Danaidas have undergone no important change in the new environment, their presence has entirely trans- formed and brought into a close superficial re- semblance to themselves the descendants of a member of an ancient group. Such a fact is in- consistent with any interpretation as yet offered except that which refers the change to the accu- mulation by selection of variations which promote a likeness to the Danaidas. The facts also bear upon the two theories of Mimicry associated with the names of H. W. Bates and Fritz Miller. According to Bates’s theory, Mimicry is a special form of protective or cryptic resemblance. In the ordinary examples of this principle, species are aided in the struggle by concealment, by a likeness to some object of no interest to their enemies (such as bark, earth, &c.); in these special examples (called mimetic) species are aided by resembling some object which is un- pleasant or even dangerous to their foes. Fritz Miller’s theory of Mimicry includes the cases in which the mimics, as well as their models, are specially defended, although generally to an DOMINANT FORMS BECOME MIMICS 175 unequal degree.! The resemblance is due to the advantages of a common advertisement. Before the growth of a mimetic likeness, Batesian mimics, it is reasonable to assume, belonged to the immense group of species possessing a cryptic appearance ; Miillerian mimics on the other hand may be assumed to have possessed warning or aposematic colours of their own previous to the adoption of those of another species. This test is more readily applied than might be supposed ; for a comparison with allied non-mimetic species, and with the non-mimetic males of mimetic females, will gene- rally indicate whether the ancestral pattern of a species now mimetic belonged to the group of concealing colours or to that of warning. The Danaidas invaded North America and entered an assemblage of butterflies of which the dominant species are ancient inhabitants of the northern land-belt. Among them are several, such as the species of Grapta or Polygonia (the ‘Comma’ butterflies), with beautifully cryptic patterns on the parts of the wing surface exposed in the rest- ing position. Nosuch forms have been influenced by the invaders, but with the whole fauna before them they have only produced changes in the dominant group Limenitis, known throughout the northern belt for a conspicuous under surface and a floating flight ; also believed to be mimicked by other butterflies, e.g. the females of the Apaturas 1 Tt is probable that relative abundance may determine the relationship of model and mimic in cases where there is no reason for suspecting any difference in the degree of unpalatability. 176 MIMICRY IN N. AMERICAN BUTTERFLIES (‘ Purple Emperors’) and the later brood of Avasch- nia levana.: Furthermore, the close allies of Li- menitis in South America, the abundant Adelphas, are beautifully mimicked, not only by females of the genus Chlorippe, which represents Apatura, but also by Erycinidae. In another point the facts are at variance with Bates’s interpretation but har- monize with Miiller’s. Bates supposed Mimicry to be an adaptation by which a scarce, hard-pressed form is enabled to hold its own in the struggle for existence. But L. arthemis, which represents with little or no change the species from which the mimics were derived, persists as a very abun- dant and flourishing species, while its mimetic descendant archippus has gained an immensely extended range and become almost universally commoner than any other species of its group (Scudder, l.c., 266). L. archippus extends from Hudson’s Bay to the Gulf of Mexico; over this vast area it is only rare in the west, and only unknown in Colorado, Arizona, and New Mexico (1.c., 278). It is to be observed that the range of archippus includes the whole of the area (Canada and the north-eastern States) occupied by the ancestral form arthemis. The facts indicate that the changes produced by the invaders were wrought in the conspicuous pattern of a dominant indigenous species, and that the transformed butterfly having adopted the 1 See also the mimetic resemblance to L. astyanax described on pp. 189-91. FACTS SUPPORT MULLER’S THEORY 177 advertisement of the still more unpalatable Danaida, became even more dominant and gained a far wider range than before. The mimetic resem- blance arose in a species which we have reason to believe possessed warning colours and some form of special protection before the change occurred. There is no evidence that the special protection was diminished after the assumption of Mimicry, and, if it remain, the new appearance is still a warning character, only one that is learnt by enemies more readily than the old because of the wide advertisement given to it by Danaida plex- ippus. The facts harmonize with the theory of Fritz Muller rather than with that of H. W. Bates. THE ‘POISON-EATING’ SWALLOW-TAIL BUTTER- FLIES (PHARMACOPHAGUS) AS MODELS FOR MIMICRY The late Erich Haase gave the name of Phar- macophagus or ‘ Poison-eater’ to the section of swallow-tail butterflies whose larvae feed upon Aristolochia or allied species, and he made the probable suggestion that the qualities which render them distasteful are derived from the juices of the food-plant. The poison-eating swallow-tails are abundant in tropical America and the Oriental Region, but with the exception of antenor in Madagascar are wanting from the Ethiopian Region. They are extensively mimicked by swallow-tails of the other two sections :—Papilio, of which machaon may be taken as a type, and N 178 MIMICRY IN N. AMERICAN BUTTERFLIES Cosmodesmus, of which podalirius serves as an example. The distinction between these three sections of Papilionidae extends to larval and pupal stages, as was originally discovered by Horsfield. It was made the basis of Haase’s classification,! recently confirmed and amplified by Rothschild and Jordan.? The latter authori- ties propose the names ‘Aristolochia Swallow- tails’, ‘ Fluted Swallow-tails’, and ‘ Kite Swallow- tails’, respectively for Haase’s sections Pharma- cophagus, Papilio, and Cosmodesmus, The Pharmacophagus swallow-tails are not so well known as models for Mimicry as are the Danainae, Acraeinae, &c., and it is therefore ex- pedient to say a few words about the section before considering the effect produced by one of its members in North America. In tropical America not only are the species of Pharmacophagus extensively mimicked but Mimicry is also strongly developed within the limits of the section itself, viz. between the two dominant groups Aeneas and Lysander. In these groups the males are commonly very different in appear- ance from the females and frequent more open habitats such as the banks of rivers, &c., the females being found in the forest. In the internal Mimicry between Aeneas and Lysander the males resemble the males, the females the females, but the female patterns are alone extensively mimicked 1 Researches on Mimicry, Pt. ii, Stuttgart, 1896, English trans- lation. ? Nov. Zool., xiii (1906), 411-752. THE ‘POISON-EATING’ MODELS 179 by other groups—Papilio, Cosmodesmus and certain Pierinae. I have as yet only come across a single example (a Cosmodesmus) in which the pattern and green markings of the males are mimicked. One or two species (e. g. Ph. hahnelt) of Pharmacophagus are themselves mimics of dominant Ithomiine genera. It has already been pointed out on p. 187 that in the Papilio mimics of Pharmacophagus the re- semblance is often attained by the females alone, a tendency exemplified in North America as shown on pp. 181-4. In Cosmodesmus, on the other hand, where the Mimicry of these models reaches a far higher level of perfection, it is equally pronounced in both sexes. In Africa, on the other hand, where, in default of Pharmacophagus models, the swallow-tails of both groups frequently mimic Danainae and Acraeinae, the resemblances attained by Cosmodesmus are far less striking than those of the other section ; yet the relationship of Mimicry to sex remains unchanged. In the Oriental Region the female Mimicry of Pharmacophagus is still characteristic of Papilio, also appearing in certain Cosmodesmus mimics of Danainae. Two remarkable features appear in this Region : (1) the development within Pharma- cophagus of the gigantic Ornithopteras which do not appear to be mimicked at all; (2) the appear- ance within the section Papilio of groups which are mimicked as extensively, perhaps even more extensively, than Pharmacophagus itself. Among N2 180 MIMICRY IN N. AMERICAN BUTTERFLIES the mimics of these Papilios are not only species of other groups in the same section but also, although in small proportion, Satyrine butterflies and day-flying moths. The fact that Pharmacophagus and certain groups of Papilio should be mimicked pre-eminently by other Papilionidae is evidence that Mimicry is most easily attained when there are initial resem- blances of size, shape, habits, and modes of flight upon which to build. PHARMACOPHAGUS (PAPILIO) PHILENOR, L., AS A MODEL FOR MIMICRY IN NORTH AMERICA Pharmacophagus is a tropical assemblage, but a few species have found their way into the northern belt in both the Old World and the New. Pharm. polydamas, with an immense range in South and Central America, also extends into the northern continent but does not there become the object of Mimicry. Pharm. philenor, ranging through Mexico and the United States (except the central district from Colorado northwards) but only as a straggler in New England and southern Canada, is on the other hand an important model for Mimicry. There is here no such interesting history of past migrations to unfold as we were able to trace in the American Danaidas. Ph. philenor is a member of the distinctively New World species of Pharmacophagus, associated together and sepa- rated from the Old World species by structural PHILENOR AN AMERICAN MODEL 181 characters. Rothschild and Jordan state that every species can be recognized as American by the examination of a single joint of one leg, and they are therefore justified in concluding that all the New World species were derived from a single ancestor possessing this character. There is no sufficient evidence that any of the numerous patterns are ancestral as compared with the others, although it is tolerably safe to conclude that the presence of hind-wing ‘ tails’ is primitive as com- pared with their absence. Following this indica- tion, we find that as a general rule the specialized and modern forms are predominant nearer to the Equator, the comparatively ancestral tailed forms occurring in latitudes more remote from it both north and south. Ph, philenor is a ‘tailed’ form, although its sub- species orswa in the Tres Marias Islands is nearly tailless. It is probably an intruder into North America from the tropics of the same Continent. It is well known to possess the characteristics of distasteful species—gregarious larvae, tenacity of life, and a strong, disagreeable scent. THE THREE PAPILIO MIMICS OF PH. PHILENOR IN NORTH AMERICA The three swallow-tail mimics of philenor belong to separate groups of Haase’s section Papilio. All of them range from the Atlantic to the Mississippi basin. 182 MIMICRY IN N. AMERICAN BUTTERFLIES The female of Papilio polyxenes asterius (Cr.) belonging to the Macnaon Group mimics philenor on both surfaces, the male on the under surface alone, except at Guerrero, Mexico, where a form (ampliata) mimetic on the upper surface is tran- sitional into the ordinary male. Papilio glaucus glaucus (L.) belongs to the Guaucus Group, next but one to the group con- taining asterius. The female is dimorphic, one form resembling the male and the other (the turnus? form, mimetic of philenor) becoming commoner in the southern part of the range. In the closely allied sub-species P. glaucus canadensis (Rothsch. and Jord.) the mimetic female form is unknown. Papilio troilus troilus (L.) belongs to the next succeeding Trortus Group, allied to the tropical and highly mimetic Ancuistapzs Group, with gregarious larvae. Both male and female of troilus mimic philenor on both wing surfaces. The most remarkable fact about these three mimics is not their moderate resemblance to the primary model philenor, but their extraordinary likeness to one another. Upon the wing or at rest at a little distance they would be indistin- guishable, and even in the cabinet they may be easily confused. It is to be expected that the species of allied groups, with patterns converging towards that of a single model, and approaching it by variations which tend to be produced in the 1 The species is commonly called P. turnus and its mimetic female the glaucus form. I follow Rothschild and J ordan in trans- posing these names. MIMICRY BETWEEN MIMICS 183 section to which they belong, should incidentally approach one another. But the strong likeness between the mimetic forms of trotlus, asterius, and glaucus seems to require something more than this, and supports the conclusion that there is secondary Mimicry between the mimics themselves. It is not necessary to repeat here the details of these secondary resemblances,' and as a matter of fact the likeness itself is stronger than might be inferred from a consideration of the details them- selves. It is necessary to see it in order to appreciate it. It is probable that troilus, mimetic in both sexes, is the oldest mimic; asterius, non-mimetic on the upper surface of the male or with very rough incipient Mimicry, the next to appear ; and glaucus, mimetic in only one form of the female, the youngest. These conclusions as to relative age are on the whole supported by the relative strength of the detailed resemblances to philenor in the three mimics. In attempting to trace the past history, here again we have the great advantage of knowing the more ancestral patterns from which the three mimics were derived :—troilus from a palamedes- like form ; asterius from the pattern of its male, which again leads back to the typical pattern of the MacHaon Group; the turnus female of glaucus from the male and non-mimetic female of the same species. 1 See Trans. Ent. Soc. Lond. (1908), 467-71. 184 MIMICRY IN N. AMERICAN BUTTERFLIES It is highly probable that the earliest steps in the direction of Mimicry in asterius and glaucus were favoured by the appearance of partially melanie varieties of the female, thus effecting suddenly that essential change which enables a butterfly with a yellow ground-colour to become the mimic of one in which it is black. But this transformation, immensely important as it is, supplies nothing more than a tinted paper for the new picture. That the melanic varieties were partial is clearly shown by the persistence (in glaucus) in a subdued and inconspicuous form of certain ancestral features that do not contribute to the Mimicry, but above all by the retention of every element in the original pattern that can be worked up into the new. By the modification of these elements in form or colour,—often in both form and colour,—the detailed mimetic pattern has been wrought upon the darkened surface. Valuable confirmation of the history suggested in the last paragraph is to be found in the dark form melasina (Rothsch. and Jord.) found in both sexes of P. polyxenes americus (Kollar), extending from North Peru to Colombia and Venezuela. This melanic variety probably represents the darkened form of asterius before the initiation of the detailed mimicry of philenor. The sub-species americus does not enter the range of philenor, and those ancestral elements which have been retained by its melanic form have not developed into the mimetic likeness seen in the more northern sub-species asterius. MIMICRY AND MELANISM 185 It is well known that all four species (including philenor) fly together. Even in my own limited experience I have taken three of them in adjacent streets on the outskirts of Chicago on the same day (Aug. 10, 1897), and the fourth in the same locality a little earlier (July 28). But precise knowledge of their relative proportions in different parts of their range would be of high interest. Again, troilus extends to the North-West Territory of Canada, probably far beyond the area in which philenor occurs as a straggler; and it would be very interesting to compare minutely large num- bers of such specimens with those from districts where the model is dominant. A similar study should be made of the Canadian specimens of asterius, although this species does not extend so far beyond the northern limits of the poison- eating model. From another point of view the interbreeding of the turnus female of glauwcus with a male from some northern district where twrnus is unknown or very scarce would be of the highest interest. We should here be able to test whether the Mendelian relationship exists between the parent form and its partially melanic variety further transformed by selection,—not a mere melanic ‘mutation’. I trust that my friend Prof. C. B. Davenport may be able to undertake this experi- ment at the Cold Spring Experimental Station. I cannot doubt that breeding could be easily carried through two generations in a large enclosed 186 MIMICRY IN N. AMERICAN BUTTERFLIES Space exposed to the sun and planted with abun- dant flowers and the food-plant of the species. It would probably be safe to use Long Island males, while female pupae or the freshly bred females themselves could be readily obtained from further south. THE EVOLUTION OF LIMENITIS (B.) ASTYANAX (F.) AS A MIMIC OF PH. PHILENOR AND ITS PAPILIO MIMICS Scudder states that L. astyanax ‘ranges from the Atlantic westward to the Mississippi Valley, and from the Gulf of Mexico northward to about the 48rd parallel of latitude”! It thus falls entirely within the area of philenor, The northern boundary of astyanax corresponds with the southern limit of its parent arthemis, and Scudder (1. c., 289) considers that they interbreed and that the intermediate form proserpina, found along the narrow belt where the two species or sub-species meet, is the resulting hybrid. Both arthemis and proserpina have been bred from the eggs of the latter. There seems little doubt that astyanax is a very recent development from arthemis in the southern part of its range,—so recent that the areas of distribution still remain distinct and parent and offspring only meet along a narrow line. It is probable that archippus arose in the same manner in part of the area of arthemis, but 1 A closely allied species or probably a form of the same species is recorded by Godman and Salvin from Mexico. EVOLUTION OF L. ASTYANAX 187 that later, after the separation had become com- plete, it spread northward over the whole range of its parent. The evolution of astyanax from arthemis was far simpler than that of archippus. The great difference in appearance between parent and offspring is brought about, as regards the upper surface, by the disappearance of the broad white band of arthemis together with all but a trace of the sub-apical white markings of the fore wings. Over and within the area formerly occupied by the white band a bluish or greenish iridescence spreads from the marginal region where it exists in arthemis. This marginal iridescence—just as in astyanax—is bluish in some individuals of arthemis, greenish in others. Reddish sub- marginal spots, although rarer in the hind wing of astyanax, are actually commoner in the fore wing than in arthemis. This curious fact, together with the evidence that astyanax and archippus may occasionally interbreed, suggests the pos- sibility of some connexion between the origins of the two mimics. The under surface of astyanax has not only similarly lost the white markings, but the chocolate-brown ground-colour of arthemis has become transformed into a dark iridescent greenish-brown. Against this background the reddish spots near the margin and base of the wings become far more conspicuous than in the parent form. The material for this transforma- 188 MIMICRY IN N. AMERICAN BUTTERFLIES tion in tint is still to be seen in the great variation of the ground-colour in arthemis. Although, as Scudder rightly maintains (1.c., 287), L. astyanax is a very poor mimic of Pharm. philenor, it bears considerable resemblance to the three Papilio mimics, especially troilus. Al- though the iridescent blue or green of its upper surface approaches rather more closely than the Papilios to the brilliant, steely lustre of philenor, it is still in this respect widely separated from the primary model and near to the mimics. The reddish spots of the under surface offer but a rough likeness to those of any of the above- named species, but there can be no doubt that their emphasis is an element in the mimetic resemblance. A careful examination of large numbers of astyanax from the extreme south of the range where it passes out of the area of glaucus and troilus but remains within that of philenor and asterius, might yield interesting results. An investigation of the proportion it bears to the four Papilionidae in various parts of their common range would also be of deep interest. Of the highest importance would be the attempt—which would probably be successful—to breed astyanax and arthemis and to ascertain whether the Mendelian proportions appear in the offspring of the hybrids. The pairing of astyanax and archippus, although in this case failure is probable, ought also to be attempted. DIANA THE MIMIC OF A MIMIC 189 THE FEMALE OF ARGYNNIS (SEMNOPSYCHE) DIANA (CR.) A MIMIC OF LIMENITIS ASTYANAX The comparatively narrow range of this species is, as Scudder points out, wholly included within that of astyanaz (l.¢., 1802). The Mimicry is confined to the upper surface, where the blue tint has even less sheen than that of any other member of the group clustered round the brilliant philenor. Apart from the blue expanse, which he admits to be mimetic, Dr. F. A. Dixey considers that the female of diana belongs to a set of dark female forms well known in Argynnis, forms which he believes to be ancestral.! It is probable that ‘the recent evolution of ZL. astyanax provided this ancestral form with a model which it could approach by small and easy steps of variation ’.? THE BEARING UPON THEORIES OF MIMICRY OF PHARM. PHILENOR AND ITS MIMICS Haase, who always shows an imperfect appre- ciation of the scope of Fritz Miiller’s principle, apparently regarded all the species mentioned in the preceding section as simple Batesian mimics of philenor, neglecting the mimetic relationships between the mimics themselves. This interpre- tation is unconvincing, and most naturalists will agree with Scudder in his hesitation to accept the two Nymphalines, astyanax and diana (female), as simple mimics of philenor. The Miillerian 1 Trans, Ent. Soc. Lond. (1890), 89-129. 2 Ibid. (1908), 475. 190 MIMICRY IN N. AMERICAN BUTTERFLIES hypothesis at once explains relationships that are mere coincidences under that of Bates. Pharm. philenor, a probable intruder from the American tropics, produced its effect upon the three large Papilios—butterflies with a conspicuous under surface pattern, in large part reproducing that of the upper surface, butterflies belonging to a section that provides models for extensive Mimicry in the Oriental Region. They may be regarded as Millerian Mimics of the primary Pharmacophagus model, exhibiting a certain amount of Secondary Mimicry of one another. The four above-named Papilionidae, but especially the three mimics acting as secondary models, then produced an effect upon L, arthemis— that same conspicuous, specially defended element in the North American butterfly fauna which was influenced in an entirely different direction by the Danaine invaders. The result of the former influence is seen in L. astyanax, a secondary mimic of the three Papilio mimics of philenor. One of the most interesting elements in this complex mimetic system is the final appearance of a tertiary mimic of astyanax, viz. the female of Argynnis diana. This was recognized by Scudder, although, not fully appreciating the Miillerian hypothesis, he was much puzzled by the fact.! The under surface of the female diana is incon- spicuous, and, considering also the restricted 1 1, ¢.,718, 1802: see, however, 266, where Scudder suggests that astyanax may possibly be specially protected. MIMICRY OF MIMICS 191 range and relative rarity of the species, it is probable that this member of the assemblage of species convergent round philenor is a Batesian mimic. But its resemblance to astyanax supports the conclusion that this latter and the sister- species archippus (and its forms) are Miillerian mimics and the parent arthemis a_ specially protected species. The resemblance of astyanar to the three species of the section Papilio, as well as the secondary resemblances between the three, similarly supports the conclusion that these mimics are Millerian. I have not hitherto called attention to the paramount need for experimental research and field observations directed to test for the presence of distasteful qualities and to estimate their effect upon enemies of the most varied kinds. It is of the utmost importance that such investigations should be undertaken on the largest possible scale. In the meantime the Millerian Hypothesis appears to explain a series of remarkable relation- ships which remain coincidences under any other hypothesis. THE RESEMBLANCES BETWEEN LIMENITIS (ADELPHA) CALIFORNICA (BUTL.) AND LIME- NITIS (NAJAS) LORQUINI (BOISD.) The examples of Mimicry which we have been considering hitherto are, with the exception of the widespread L. archippus, characteristic of the eastern side of North America. The present 192 MIMICRY IN N. AMERICAN BUTTERFLIES instance, the last of the examples known in this portion of the northern land-belt, is found on the Pacific coast. The resemblances are somewhat crude but of quite remarkable interest. LInmenitis californica, because of its pattern and colouring, is often placed in Adelpha, a large genus with over seventy species all confined to tropical America. Adelpha is separated from the closely allied northern genus Limenitis by the hairiness of the eyes in front. Californica is by this character as well as its more northern range associated with the heterogeneous assemblage ‘ Limenitis’, which so much requires a thorough revision. In adopting this view I accept the posi- tion assigned to the species by Scudder in 1875.1 Closely allied to californica, of Oregon, Cali- fornia, and Nevada, is ZL. bredowt (Hiibn.) of Arizona, Mexico, and Guatemala. A much needed investigation is the determination whether these two forms meet, and interbreed along the line of contact. The southern species or sub-species bredowi, is associated in Mexico and Guatemala with many true species of Adelpha of which no less than thirty-one extend into Central America. To these it, and to a less extent the northern cali- fornica, bear much likeness, especially to A. dyonysa (Hew.), massilia (Feld), lerna (Hew.), and Jessonia (Hew.). This likeness is probably a mimetic resemblance which extends beyond the 1 Bull. Buffalo Soc. N. Sc. (Feb., 1875), 238. MIMICRY ON THE PACIFIC COAST 193 range of the models into Arizona, and, with diminished effect, still further north into the allied sub-species. Although the details of the resemblance leave little doubt that this interpre- tation is correct for the southern bredowi, it is possible that californica represents an ancestral form connecting the Adelphas with Limenitis, a form left isolated and comparatively unchanged in the north,! while its southern allies have been modified by the presence of the dominant Adelphas. At any rate in one feature neither sub-species appears to be mimetic, viz. in the yellowish tint of the conspicuous band crossing both wings; for in all the Central American Adelphas at all resembling them this marking is pure white or bluish-white. We cannot hope to determine how far the pattern of californica is ancestral until the structural relationships and the early stages of Limenitis in the widest sense and Adelpha have been most minutely investigated. Limenitis lorquint, occurring with L. californica in Nevada, California, and Oregon, also extends far north of this species into British Columbia and Vancouver Island. Among all the North American species of Limenitis it is the one which comes nearest to the Old World forms, as Scudder recognized when he included it with the European L. populi in the genus Najas, separating all the other American forms of Limenitis except cali- 1 See, however, pp. 198-9. 10) 194. MIMICRY IN N. AMERICAN BUTTERFLIES Jornica and Basilarchia. Even such fleeting charac- ters as the markings show the Old World affinities of lorguini in the strong development of the pale spot in the fore wing cell and the position and form of the pale band crossing both wings. It is to be noted furthermore that its distribution, and especially its extension north- ward, along the Pacific coast, bring lorquini into closest proximity to the Old World species. In certain important respects the upper surface pattern of ZL. lorquinit is certainly mimetic of californica :— The conspicuous fulvous apical area of the fore wing; the yellowish tint of the band crossing both wings; and, although here the interpretation is less certain, the fulvous marking at the anal angle of the hind wing. 1. In the first and most important of these points of superficial resemblance there is, so far as my experience goes, a much greater average development of the fulvous patch in specimens of lorquini which enter the range of californica in Oregon and California than in those which come from Canada, entirely beyond the range of the model. The close relationship between californica and lorquint may incline naturalists to look on their resemblance as due to affinity and not to Mimicry. ‘It is commonly forgotten that mimicry, being independent of affinity, occurs between forms of all degrees of relationship, the closest as well as LORQUINI MIMICS CALIFORNICA 195 the most remote’;! although of course the latter are easy to interpret, while the former may be excessively difficult. In this case, however, there is neither doubt nor difficulty, for not only is there the geographical coincidence between the model and the average increase of the marking in the mimic, but the fulvous apical marking of lorquinti—of a somewhat richer, deeper shade than the tawny patch of californica—is due to the in- ward growth of a marginal marking, while that of the model occupies a clearly defined sub- marginal and sub-apical position. The resem- blance is, in fact, produced by markings which are essentially different; yet in some of the southern examples of lorquini in which the mark- ings extend inward to the greatest distance the superficial resemblance is very considerable. The above-stated conclusion that the chief mimetic element of lorquini is on the average subject to considerable strengthening in the southern part of its range, is founded on an examination of the few dozen specimens I have been able to study in English collections, and especially the Godman-Salvin material in the British Museum. I now trust that the subject may be taken up by American naturalists and many hundreds of specimens compared from all parts of the north and south range of the species. 2. In the second point also, the yellowish tint 1 Trans. Ent. Soc. Lond, (1908), 482. 02 196 MIMICRY IN N. AMERICAN BUTTERFLIES of the principal band, the resemblance is certainly mimetic and not due to affinity; for lorquini, ancestral in certain other features, has here lost the original whiteness of this marking, preserved not only in the Old World but in Limenitis arthemis and L. weidermeyeri (Edw.) of the New. An excessively slight deepening of the yellow tint could be made out in southern individuals from the area occupied by the model. In order to detect the difference, a long series of northern specimens should be placed beside a similar series from the south and the two compared in a strong light. But far larger numbers than I have seen ought to be examined from this point of view, and, if it were possible to make it, the comparison of perfectly fresh specimens would be most desirable. 3. The fulvous marking at the anal angle of the hind wing is excessively variable and often absent from specimens in all parts of the range. The comparison of a very large amount of mate- rial is necessary before we can reach any safe conclusions as to the existence of mimetic re- semblance in this feature, and the same is true of the extremely variable under surface of lor- quini, in which the development of the inner row of sub-marginal bluish lunules may be mime- tic of californica. This feature was generally suppressed in the Vancouver Island specimens I have seen. We now come to the consideration of certain PROBABLE RECIPROCAL MIMICRY 197 differences between L. californica and its southern form bredowi which promote a likeness to lorquini. If these are not mere coincidences, we can hardly escape the conclusion that there is Reciprocal Mimicry (Diaposematism) between californica and bredowt. 1. The wings of both sexes of californica are more rounded than those of the males of bredowi, in this respect resembling both sexes of lorquini. The fact that the southern females have rounded wings may indicate that this character is ances- tral in both sexes, the males alone having been modified in Mimicry of Adelpha. But it is a probable hypothesis that the presence of lorquini has prevented this mimetic feature from passing northward into the males of californica. It does pass far beyond