SUMMARY OF THE PAST CHANGES AND GENERAL RELATIONS OF THE SEVERAL REGIONS.
Having now closed our survey of the animal life of the whole earth—a survey which has necessarily been encumbered with a multiplicity of detail—we proceed to summarize the general conclusions at which we have arrived, with regard to the past history and mutual relations of the great regions into which we have divided the land surface of the globe.
All the palæontological, no less than the geological and physical evidence, at present available, points to the great land masses of the Northern Hemisphere as being of immense antiquity, and as the area in which the higher forms of life were developed. In going back through the long series of the Tertiary formations, in Europe, Asia, and North America, we find a continuous succession of vertebrate forms, including all the highest types now existing or that have existed on the earth. These extinct animals comprise ancestors or forerunners of all the chief forms now living in the Northern Hemisphere; and as we go back farther and farther into the past, we meet with ancestral forms of those types also, which are now either confined to, or specially characteristic of, the land masses of the Southern Hemisphere. Not only do we find that elephants, and rhinoceroses, and hippopotami, were once far more abundant in Europe than they are now in the tropics, but we also find that the apes of West Africa and Malaya, the lemurs of Madagascar, the Edentata of Africa and South America, and theMarsupials of America and Australia, were all represented in Europe (and probably also in North America) during the earlier part of the Tertiary epoch. These facts, taken in their entirety, lead us to conclude that, during the whole of the Tertiary and perhaps during much of the Secondary periods, the great land masses of the earth were, as now, situated in the Northern Hemisphere; and that here alone were developed the successive types of vertebrata from the lowest to the highest. In the Southern Hemisphere there appear to have been three considerable and very ancient land masses, varying in extent from time to time, but always keeping distinct from each other, and represented, more or less completely, by Australia, South Africa, and South America of our time. Into these flowed successive waves of life, as they each in turn became temporarily united with some part of the northern land. Australia appears to have had but one such union, perhaps during the middle or latter part of the Secondary epoch, when it received the ancestors of its Monotremata and Marsupials, which it has since developed into a great variety of forms. The South African and South American lands, on the other hand, appear each to have had several successive unions and separations, allowing first of the influx of low forms only (Edentata, Insectivora and Lemurs); subsequently of Rodents and small Carnivora, and, latest of all, of the higher types of Primates, Carnivora and Ungulata.
During the whole of the Tertiary period, at least, the Northern Hemisphere appears to have been divided, as now, into an Eastern and a Western continent; always approximating and sometimes united towards the north, and then admitting of much interchange of their respective faunas; but on the whole keeping distinct, and each developing its own special family and generic types, of equally high grade, and generally belonging to the same Orders. During the Eocene and Miocene periods, the distinction of the Palæarctic and Nearctic regions was better marked than it is now; as is shown by the floras no less than by the faunas of those epochs. Dr. Newberry, in his Report on the Cretaceous and Tertiary floras of the Yellowstone and Missouri Rivers, states, that although the Miocene flora of Central NorthAmerica corresponds generally with that of the European Miocene, yet many of the tropical, and especially the Australian types, such asHakeaandDryandra, are absent. Owing to the recent discovery of a rich Cretaceous flora in North America, probably of the same age as that of Aix-la-Chapelle in Europe, we are able to continue the comparison; and it appears, that at this early period the difference was still more marked. The predominant feature of the European Cretaceous flora seems to have been the abundance of Proteaceæ, of which seven genera now living in Australia or the Cape of Good Hope have been recognised, besides others which are extinct. There are also several species ofPandanus, or screw-pine, now confined to the tropics of the Eastern Hemisphere, and along with these, oaks, pines, and other more temperate forms. The North American Cretaceous flora, although far richer than that of Europe, contains no Proteaceæ orPandani, but immense numbers of forest trees of living and extinct genera. Among the former we have oaks, beeches, willows, planes, alders, dog-wood, and cypress; together with such American forms as magnolias, sassafras, and liriodendrons. There are also a few not now found in America, asAraucariaandCinnamomum, the latter still living in Japan. This remarkable flora has been found over a wide extent of country—New Jersey, Alabama, Kansas, and near the sources of the Missouri in the latitude of Quebec—so that we can hardly impute its peculiarly temperate character to the great elevation of so large an area. The intervening Eocene flora approximates closely, in North America, to that of the Miocene period; while in Europe it seems to have been fully as tropical in character as that of the preceding Cretaceous period; fruits ofNipa,Pandanus,Anona,Acacia, and many Proteaceæ, occurring in the London clay at the mouth of the Thames.
These facts appear, at first sight, to be inconsistent, unless we suppose the climates of Europe and North America to have been widely different in these early times; but they may perhaps be harmonised, on the supposition of a more uniform and a somewhat milder climate then prevailing over the whole Northern Hemisphere; the contrast in the vegetation of these countriesbeing due to a radical difference of type, and therefore not indicative of climate. The early European flora seems to have been a portion of that which now exists only in the tropical and sub-tropical lands of the Eastern Hemisphere; and, as much of this flora still survives in Australia, Tasmania, Japan, and the Cape of Good Hope, it does not necessarily imply more than a warm and equable temperate climate. The early North American flora, on the other hand, seems to have been essentially the same in type as that which now exists there, and which, in the Miocene period, was well represented in Europe; and it is such as now flourishes best in the warmer parts of the United States. But whatever conclusion we may arrive at on the question of climate, there can be no doubt as to the distinctness of the floras of the ancient Nearctic and Palæarctic regions; and the view derived from our study of their existing and extinct faunas—that these two regions have, in past times, been more clearly separated than they are now—receives strong support from the unexpected evidence now obtained as to the character and mutations of their vegetable forms, during so vast an epoch as is comprised in the whole duration of the Tertiary period.
The general phenomena of the distribution of living animals, combined with the evidence of extinct forms, lead us to conclude that the Palæarctic region of early Tertiary times was, for the most part, situated beyond the tropics, although it probably had a greater southward extension than at the present time. It certainly included much of North Africa, and perhaps reached far into what is now the Sahara; while a southward extension of its central mass may have included the Abyssinian highlands, where some truly Palæarctic forms are still found. This is rendered probable by the fossils of Perim Island a little further east, which show that the characteristic Miocene fauna of South Europe and North India prevailed so far within the tropics. There existed, however, at the extreme eastern and western limits of the region, two extensive equatorial land-areas, our Indo-Malayan and West African sub-regions—both of which must have been united for more or less considerable periods with the northern continent. They would then have receivedfrom it such of the higher vertebrates as were best adapted for the peculiar climatal and organic conditions which everywhere prevail near the equator; and these would be preserved, under variously modified forms, when they had ceased to exist in the less favourable and constantly deteriorating climate of the north. At later epochs, both these equatorial lands became united to some part of the great South African continent (then including Madagascar), and we thus have explained many of the similarities presented by the faunas of these distant, and generally very different countries.
During the Miocene period, when a subtropical climate prevailed over much of Europe and Central Asia, there would be no such marked contrast as now prevails between temperate and tropical zones; and at this time much of our Oriental region, perhaps, formed a hardly separable portion of the great Palæarctic land. But when, from unknown causes, the climate of Europe became less genial, and when the elevation of the Himalayan chain and the Mongolian plateau caused an abrupt difference of climate on the northern and southern sides of that great mountain barrier, a tropical and a temperate region were necessarily formed; and many of the animals which once roamed over the greater part of the older and more extensive region, now became restricted to its southern or northern divisions respectively. Then came the great change we have already described (vol. i. p. 288), opening the newly-formed plains of Central Africa to the incursions of the higher forms of Europe; and following on this, a still further deterioration of climate, resulting in that marked contrast between temperate and tropical faunas, which is now one of the most prominent features in the distribution of animal as well as of vegetable forms.
It is not necessary to go into any further details here, as we have already, in our discussion of the origin of the fauna of the several regions, pointed out what changes most probably occurred in each case. These details are, however, to a great extent speculative; and they must remain so till we obtain as much knowledge of the extinct faunas and past geological history of the southern lands, as we have of those of Europe and NorthAmerica. But the broad conclusions at which we have now arrived seem to rest on a sufficiently extensive basis of facts; and they lead us to a clearer conception of the mutual relations and comparative importance of the several regions than could be obtained at an earlier stage of our inquiries.
If our views of the origin of the several regions are correct, it is clear that no mere binary division—into north and south, or into east and west—can be altogether satisfactory, since at the dawn of the Tertiary period we still find our six regions, or what may be termed the rudiments of them, already established. The north and south division truly represents the fact, that the great northern continents are the seat and birth-place of all the higher forms of life, while the southern continents have derived the greater part, if not the whole, of their vertebrate fauna from the north; but it implies the erroneous conclusion, that the chief southern lands—Australia and South America—are more closely related to each other than to the northern continent. The fact, however, is that the fauna of each has been derived, independently, and perhaps at very different times, from the north, with which they therefore have a true genetic relation; while any intercommunion between themselves has been comparatively recent and superficial, and has in no way modified the great features of animal life in each. The east and west division, represents—according to our views—a more fundamental diversity; since we find the northern continent itself so divided in the earliest Eocene, and even in Cretaceous times; while we have the strongest proof that South America was peopled from the Nearctic, and Australia and Africa from the Palæarctic region: hence, the Eastern and Western Hemispheres are the two great branches of the tree of life of our globe. But this division, taken by itself, would obscure the facts—firstly, of the close relation and parallelism of the Nearctic and Palæarctic regions, not only now but as far back as we can clearly trace them in the past; and, secondly, of the existing radical diversity of the Australian region from the rest of the Eastern Hemisphere.
Owing to the much greater extent of the old Palæarctic region (including our Oriental), and the greater diversity ofMammalia it appears to have produced, we can have little doubt that here was the earliest seat of the development of the vertebrate type; and probably of the higher forms of insects and land-molluscs. Whether the Nearctic region ever formed one mass with it, or only received successive immigrations from it by northern land-connections both in an easterly and westerly direction, we cannot decide; but the latter seems the most probable supposition. In any case, we must concede the first rank to the Palæarctic and Oriental regions, as representing the most important part of what seems always to have been the Great Continent of the earth, and the source from which all the other regions were supplied with the higher forms of life. These once formed a single great region, which has been since divided into a temperate and a tropical portion, now sufficiently distinct; while the Nearctic region has, by deterioration of climate, suffered a considerable diminution of productive area, and has in consequence lost a number of its more remarkable forms. The two temperate regions have thus come to resemble each other more than they once did, while the Oriental retains more of the zoological aspect of the great northern regions of Miocene times. The Ethiopian, from having been once an insular region, where lower types of vertebrates alone prevailed, has been so overrun with higher types from the old Palæarctic and Oriental lands that it now rivals, or even surpasses, the Oriental region in its representation of the ancient fauna of the great northern continent. Both of our tropical regions of the Eastern Hemisphere possess faunas which are, to some extent, composite, being made up in different proportions of the productions of the northern and southern continents,—the former prevailing largely in the Oriental, while the latter constitutes an important feature in the Ethiopian fauna. The Neotropical region has probably undergone great fluctuations in early times; but it was, undoubtedly, for long periods completely isolated, and then developed the Edentate type of Mammals and the Formicaroid type of Passerine birds into a variety of forms, comparable with the diversified Marsupials of Australia, and typical Passeres of the Eastern Hemisphere.It has, however, received successive infusions of higher types from the north, which now mingle in various degrees with its lower forms. At an early period it must have received a low form of Primates, which has been developed into the two peculiar families of American monkeys; while its llamas, tapirs, deer, and peccaries, came in at a later date, and its opossums and extinct horses probably among the latest. The Australian region alone, after having been united with the great northern continent at a very early date (probably during the Secondary period) has ever since remained more or less completely isolated; and thus exhibits the development of a primeval type of mammal, almost wholly uninfluenced by any incursions of a later and higher type. In this respect it is unique among all the great regions of the earth.
We see, then, that each of our six regions has had a history of its own, the main outlines of which we have been able to trace with tolerable certainty. Each of them is now characterised—as it seems to have been in all past time of which we have any tolerably full record—by well-marked zoological features; while all are connected and related in the complex modes we have endeavoured to unravel. To combine any two or more of these regions, on account of existing similarities which are, for the most part, of recent origin, would obscure some of the most important and interesting features of their past history and present condition. And it seems no less impracticable to combine the whole into groups of higher rank; since it has been shown that there are two opposing modes of doing this, and that each of them represents but one aspect of a problem, which can only be solved by giving equal attention to all its aspects.
For reasons which have been already stated, and which are sufficiently obvious, we have relied almost exclusively on the distribution of living and extinct mammalia, in arriving at these conclusions. But we believe they will apply equally to elucidate the phenomena presented by the distribution of all terrestrial organisms, when combined with a careful consideration of thevarious means of dispersal of the different groups, and the comparative longevity of their species and genera. Even insects, which are perhaps of all animals the farthest removed from mammalia in this respect, agree, in the great outlines of their distribution, with the vertebrate orders. The Regions are admittedly the same, or nearly the same for both; and the discrepancies that occur are of a nature which can be explained by two undoubted facts—the greater antiquity, and the greater facilities for dispersal, of insects.
But this principle, if sound, must be carried farther, and be applied to plants also. There are not wanting indications that this may be successfully done; and it seems not improbable, that the reason why botanists have hitherto failed to determine, with any unanimity, which are the most natural phytological regions, and to work out any connected theory of the migrations of plants, is, because they have not been furnished with the clue to the past changes of the great land masses, which could only be arrived at by such an examination of the past and present distribution of the higher animals as has been here attempted. The difficulties in the way of the study of the distribution of plants, from this point of view, will be undoubtedly very great; owing to the unusual facilities for distribution many of them possess, and the absence of any group which might take the place of the mammalia among animals, and serve as a guide and standard for the rest. We cannot expect the regions to be so well defined in the case of plants as in that of animals; and there are sure to be many anomalies and discrepancies, which will require long study to unravel. The Six Great Regions here adopted, are however, as a whole, very well characterised by their vegetable forms. The floras of tropical America, of Australia, of South Africa, and of Indo-Malaya, stand out with as much individuality as do the faunas; while the plants of the Palæarctic and Nearctic regions, exhibit resemblances and diversities, of a character not unlike those found among the animals.
This is not a mere question of applying to the vegetable kingdom a series of arbitrary divisions of the earth which have beenfound useful to zoologists; for it really involves a fundamental problem in the theory of evolution. The question we have to answer, is, firstly—whether the distribution of plants is, like that of animals, mainly and primarily dependent on the past revolutions of the earth's surface; or, whether other, and altogether distinct causes, have had a preponderating influence in determining the range and limits of vegetable forms; and, secondly—whether those revolutions have been, in their general outlines, correctly interpreted by means of a study of the distribution and affinities of the higher animals. The first question is one for botanists alone to answer; but, on the second point, the author ventures to hope for an affirmative reply, from such of his readers as will weigh carefully the facts and arguments he has adduced.
The remaining part of this volume, will consist, of a systematic review of the distribution of each family of animals, and an application of the principles already established to elucidate the chief phenomena they present. The present chapter must, therefore, be considered as the conclusion of the argumentative and theoretical part of the present work; but it must be read in connection with the various discussions in Parts II. and III., in which the conclusions to be drawn from the several groups of facts have been successively given;—and especially in connection with the general observations at the end of each of the six chapters on the Zoological Regions.
The hypothetical view, as to the more recent of the great Geographical changes of the Earth's surface, here set forth, is not the result of any preconceived theory, but has grown out of a careful study of the facts accumulated, and has led to a considerable modification of the author's previous views. It may be described, as an application of the general theory of Evolution, to solve the problem of the distribution of animals; but it also furnishes some independent support to that theory, both by showing what a great variety of curious facts are explained by its means, and by answering some of the objections,which have been founded on supposed difficulties in the distribution of animals in space and time.
It also illustrates and supports the geological doctrine, of the general permanence of our great continents and oceans, by showing how many facts in the distribution of animals can only be explained and understood on such a supposition; and it exhibits, in a striking manner, the enormous influence of the Glacial epoch, in determining the existing zoological features of the various continents.
And, lastly, it furnishes a more consistent and intelligible idea than has yet been reached by any other mode of investigation, of all the more important changes of the earth's surface that have probably occurred during the entire Tertiary period; and of the influence of these changes, in bringing about the general features, as well as many of the more interesting details and puzzling anomalies, of the Geographical Distribution of Animals.
PART IV.
GEOGRAPHICAL ZOOLOGY:
A SYSTEMATIC SKETCH OF THE CHIEF FAMILIES OF LAND ANIMALS IN THEIR GEOGRAPHICAL RELATIONS.
INTRODUCTION.
In the preceding part of our work, we have discussed the geographical distribution of animals from the point of view of the geographer; taking the different regions of the earth in succession, and giving as full an account as our space would permit of their chief forms of animal life. Now, we proceed from the standpoint of the systematic zoologist; taking in succession each of the families with which we deal, and giving an account of the distribution, both of the entire family and, as far as practicable, of each of the genera of which it is composed. As in the former part, our mode of treatment led us to speculate on the past changes of the earth's surface; so here we shall endeavour to elucidate the past migrations of animals, and thus, to some extent, account for their actual distribution.
The tabular headings, showing the range of the family in each region, will enable the reader to determine at a glance the general distribution of the group, as soon as he has familiarised himself, by a study of our general and regional maps, with the limits of the regions and sub-regions, and the figures (1 to 4) by which the latter are indicated. Much pains have been taken, to give the number of the known genera and species in each family, correctly; but these numbers must, in most cases, only be looked upon as approximations; because, owing to constant accessions of fresh material on the one hand, and the discovery that many supposed species are only varieties, on the other, such statistics are in a continual state of fluctuation. In the number of genera there is the greatest uncertainty; as will be seen by the two sets of numbers sometimes given, which denote the genera according to different modern authorities.
There is also a considerable difference in the dependence to be placed on the details given in the different classes of animals. In Mammalia and Birds some degree of accuracy has, it is hoped, been attained; the classification of these groups being much advanced, and the materials for their study ample. In Reptiles this is not the case, as there is no recently published work dealing with the whole subject, or with either of the larger orders. An immense number of new species and new genera of snakes and lizards, have been described in the last twenty years; and Dr. Günther—our greatest authority on reptiles in this country—has kindly assisted me in incorporating such of these as are most trustworthy, in a general system; but until entire Orders have been described or catalogued on a uniform plan, nothing more than a general approximation to the truth can be arrived at. Still, so many of the groups are well defined, and have a clearly limited distribution, that some interesting and valuable comparisons may be made.
For Fishes, the valuable "Catalogue" of Dr. Günther was available, and it has rarely been attempted to go beyond it. A large number of new species have since been described, in all parts of the world; but it is impossible to say how many of these are really new, or what genera they actually belong to. The part devoted to this Class is, therefore, practically a summary of Dr. Günther's Catalogue; and it is believed that the discoveries since made will not materially invalidate the conclusions to be drawn from such a large number of species, which have been critically examined and classified on a uniform system by one of our most able naturalists. When a supplement to this catalogue is issued, it will be easier to make the necessary alterations in distribution, than if a mass of untrustworthy materials had been mixed up with it.
For Insects, excellent materials are furnished, in the Catalogue of Mr. Kirby for Butterflies and in that of Drs. Gemminger and Harold for Coleoptera. I have also made use of some recently published memoirs on the Insects of Japan and St. Helena, and a few other recent works; and have, I believe, elaborated a more extensive series of facts to illustrate the distribution of insects,than has been made use of by any previous writer. Several discussions on the bearing of the facts of insect distribution, will also be found under the several Regions, in the preceding part of this work.
Terrestrial Mollusca form a group, as to the treatment of which I have most misgivings; owing to my almost entire ignorance of Malacology, and the great changes recently made in the classification of shells. There is also much uncertainty as to genera and sub-genera, which is very puzzling to one who merely wishes to get at general results. Finding it impossible to incorporate the new matter with the old, or to harmonise the different classifications of modern conchologists, I thought it better to confine myself to the standard works of Martens and Pfeiffer, with such additions of new species as I could make without fear of going far wrong. In some cases I have made use of recent monographs—especially on the shells of Europe, North America, the West Indian Islands, and the Sandwich Islands; and have, I venture to hope, not fallen into much error in the general conclusions at which I have arrived.
THE DISTRIBUTION OF THE FAMILIES AND GENERA OF MAMMALIA.
Order I.—PRIMATES.
Family1.—SIMIIDÆ. (4 Genera, 12 Species).
The Simiidæ, or Anthropoid Apes, comprehend those forms of the monkey-tribe which, in general organization, approach nearest to man. They inhabit the tropics of the Old World, and are most abundant near the equator; but they are limited to certain districts, being quite unknown in eastern and southern Africa, and the whole peninsula of Hindostan.
The genusTroglodytes(orMimetes, as it is sometimes named) comprehends the chimpanzee and gorilla. It is confined to the West African sub-region, being found on the coast about 12° North and South of the equator, from the Gambia to Benguela, and as far inland as the great equatorial forests extend. There are perhaps other species of chimpanzee; since Livingstone met with what he supposed to be a new species in the forest region west of Lake Tanganyika, while Dr. Schweinfurth found one in the country beyond the western watershed of the Nile. The gorilla is confined within narrower limits on and near the equator.
We have to pass over more than 70° of longitude before we again meet with Anthropoid Apes, in the northern part of Sumatra—where a specimen of the orang-utan (Simia satyrus) now in the Calcutta Museum, was obtained by Dr. Abel, and described by him in theAsiatic Researches, vol. xv.—and in Borneo, from which latter island almost all the specimens in European museums have been derived. There are supposed to be two species ofSimiain Borneo, a larger and a smaller; but their distinctness is not admitted by all naturalists. Both appear to be confined to the swampy forests near the north, west, and south coasts.
The Gibbons, or long-armed apes, forming the genusHylobates, (7 species) are found in all the large islands of the Indo-Malayan sub-region, except the Philippines; and also in Sylhet and Assam south of the Brahmaputra river, eastward to Cambodja and South China to the west of Canton, and in the island of Hainan.
The Siamang (Siamanga syndactyla) presents some anatomical peculiarities, and has the second and third toes united to the last joint, but in general form and structure it does not differ fromHylobates. It is the largest of the long-armed apes, and inhabits Sumatra and the Malay peninsula.
Family2.—SEMNOPITHECIDÆ. (2 Genera, 30 Species.)
The Semnopithecidæ, are long-tailed monkeys without cheek-pouches, and with rather rounded faces, the muzzle not being prominent. They have nearly the same distribution as the last family, but are more widely dispersed in both Africa and Asia, one species just entering the Palæarctic region.
The Eastern genusPresbytesorSemnopithecus(29 species), is spread over almost the whole of the Oriental region wherever the forests are extensive. They extend along the Himalayas to beyond Simla, where a species has been observed at an altitude of 11,000feet, playing among fir-trees laden with snow wreaths. On the west side of India they are not found to the north of 14° N. latitude. On the east they extend into Arakan, and to Borneo and Java, but not apparently into Siam or Cambodja. Along the eastern extension of the Himalayas they again occur in East Thibet; a remarkable species with a large upturned nose (S. roxellana) having been discovered by Père David at Moupin (about Lat. 32° N.) in the highest forests, where the winters are severe and last for several months, and where the vegetation, and the other forms of animal life, are wholly those of the Palæarctic region. It is very curious that this species should somewhat resemble the young state of the proboscis monkey (S. nasalis), which inhabits one of the most uniform, damp, and hot climates on the globe—the river-swamps of Borneo.
Colobus, the African genus (11 species), is very closely allied to the preceding, differing chiefly in the thumb being absent or rudimentary. They are confined to the tropical regions—Abyssinia on the east, and from the Gambia to Angola and the island of Fernando Po, on the west.
Family3.—CYNOPITHECIDÆ. (7 Genera, 67 Species).
This family comprehends all the monkeys with cheek pouches, and the baboons. Some of these have very long tails, some none; some are dog-faced, others tolerably round-faced; but there are so many transitions from one to the other, and such a general agreement in structure, that they are now considered to form a very natural family. Their range is more extensive than any other family of Quadrumana, since they not only occur in every part of the Ethiopian and Oriental regions, but enter the Palæarctic region in the east and west, and the Australian region as far as the islands of Timor and Batchian. The African generaareMyiopithecus,Cercopithecus,Cercocebus,Theropithecus, andCynocephalus; the Oriental genera,Macacus, andCynopithecus.
Myiopithecus(1 species), consisting of the talapoin monkey of West Africa, differs from the other African monkeys in the structure of the last molar tooth; in the large ears, short face, and wide internasal septum; in this respect, as well as in its grace and gentleness, resembling some of the American monkeys.
Cercopithecus(24 species), contains all the more graceful and prettily coloured monkeys of tropical Africa, and comprises the guenons, the white-nosed, and the green monkeys. They range from the Gambia to the Congo, and from Abyssinia to the Zambesi.
Cercocebus(5 species), the mangabeys, of West Africa, are very closely allied to the eastern genusMacacus.
Theropithecus(2 species), including the gelada of Abyssinia and an allied species, resemble in form the baboons, but have the nostrils placed as in the last genus.
Cynocephalus(10 species), the baboons, are found in all parts of Africa. They consist of animals which vary much in appearance, but which agree in having an elongated dog-like muzzle with terminal nostrils, and being of terrestrial habits. Some of the baboons are of very large size, the mandrill (C. maimon) being only inferior to the orang and gorilla.
Macacus(25 species), is the commonest form of eastern monkey, and is found in every part of the Oriental region, as well as in North Africa, Gibraltar, Thibet, North China, and Japan; and one of the commonest species,M. cynomolgus, has extended its range from Java eastward to the extremity of Timor. The tail varies greatly in length, and in the Gibraltar monkey (M. innus) is quite absent. A remarkable species clothed with very thick fur, has lately been discovered in the snowy mountains of eastern Thibet.
Cynopithecus(? 2 sp.).—This genus consists of a black baboon-like Ape, inhabiting Celebes, Batchian, and the Philippine Islands; but perhaps introduced by man into the latter islands and into Batchian. It is doubtful if there is more than one species. The tail of this animal is a fleshy tubercle, the nostrils as inMacacus, but the muzzle is very prominent; and thedevelopment of the maxillary bones into strong lateral ridges corresponds to the structure of the most typical baboons. This species extends further east than any other quadrumanous animal.
Family4.—CEBIDÆ. (10 Genera, 78 Species.)
The Cebidæ, which comprehend all the larger American Monkeys, differ from those of the Old World by having an additional molar tooth in each jaw, and a broad nasal septum; while they have neither cheek-pouches nor ischial callosities, and the thumb is never completely opposable. Some have prehensile tails, especially adapting them for an arboreal life. They are divided into four sub-families,—Cebinæ, Mycetinæ, Pitheciinæ, and Nyctipithecinæ. The Cebidæ are strictly confined to the forest regions of tropical America, from the southern part of Mexico to about the parallel of 30° South Latitude. The distribution of the genera is as follows:—
Sub-family, Cebinæ.—Cebus(18 sp.), is the largest genus of American monkeys, and ranges from Costa Rica to Paraguay. They are commonly called sapajous.Lagothrix(5 sp.), the woolly monkeys, are rather larger and less active than the preceding; they are confined to the forests of the Upper Amazon Valley, and along the slopes of the Andes to Venezuela and Bolivia.Ateles(14 sp.), the spider monkeys, have very long limbs and tail. They range over the whole area of the family, and occur on the west side of the Equatorial Andes and on the Pacific coast of Guatemala.Eriodes(3 sp.), are somewhat intermediate between the last two genera, and are confined to the eastern parts of Brazil south of the equator. The three last mentioned genera have very powerful prehensile tails, the end being bare beneath; whereas the species ofCebushave the tailcompletely covered with hair, although prehensile, and therefore not so perfect a grasping organ.
Sub-family, Mycetinæ, consists of but a single genus,Mycetes(10 sp.), the howling monkeys, characterized by having a hollow bony vessel in the throat formed by an enlargement of the hyoid bone, which enables them to produce a wonderful howling noise. They are large, heavy animals, with a powerful and perfect prehensile tail. They range from East Guatemala to Paraguay. (Plate XIV., vol. ii., p.24.)
Sub-family, Pitheciinæ, the sakis, have a non-prehensile bushy tail.Pithecia(7 sp.), has the tail of moderate length; whileBrachiurus(5 sp.) has it very short. Both appear to be restricted to the great equatorial forests of South America.
Sub-family, Nyctipithecinæ, are small and elegant monkeys, with long, hairy, non-prehensile tails.Nyctipithecus(5 sp.), the night-monkeys or douroucoulis, have large eyes, nocturnal habits, and are somewhat lemurine in their appearance. They range from Nicaragua to the Amazon and eastern Peru.SaimirisorChrysothrix(3 sp.), the squirrel-monkeys, are beautiful and active little creatures, found in most of the tropical forests from Costa Rica to Brazil and Bolivia.Callithrix(11 sp.), are somewhat intermediate between the last two genera, and are found all over South America from Panama to the southern limits of the great forests.
Family5.—HAPALIDÆ. (2 Genera, 32 Species.)
The Hapalidæ, or marmosets, are very small monkeys, which differ from the true Cebidæ in the absence of one premolar tooth, while they possess the additional molar tooth; so that while they have the same number of teeth (thirty-two) as the Old World monkeys, they differ from them even more than do theCebidæ. The thumb is not at all opposable, and all the fingers are armed with sharp claws. The hallux, or thumb-like great toe, is very small; the tail is long and not prehensile. The two generaHapale(9 sp.), andMidas(24 sp.), are of doubtful value, though some naturalists have still further sub-divided them. They are confined to the tropical forests of South America, and are most abundant in the districts near the equator.
Sub-order—LEMUROIDEA.
Family6.—LEMURIDÆ. (11 Genera, 53 Species.)
The Lemuridæ, comprehending all the animals usually termed Lemurs and many of their allies, are divided by Professor Mivart—who has carefully studied the group—into four sub-families and eleven genera, as follows:—
Sub-familyIndrisinæ, consisting of the genusIndris(5 sp.), is confined to Madagascar.
Sub-familyLemurinæ, contains five genera, viz.:—Lemur, (15 sp.);Hapalemur(2 sp.);Microcebus(4 sp.);Chirogaleus(5 sp.); andLepilemur(2 sp.);—all confined to Madagascar.
Sub-familyNycticebinæ, contains four genera, viz.:—Nycticebus(3 sp.)—small, short-tailed, nocturnal animals, called slow-lemurs,—range from East Bengal to South China, and to Borneo and Java;Loris(1 sp.)—a very small, tail-less, nocturnal lemur, which inhabits Madras, Malabar, and Ceylon;Perodicticus(1 sp.)—the potto—a small lemur with almost rudimentary forefinger, found at Sierra Leone (Plate V., vol. i., p. 264);Arctocebus(1 sp.)—the angwantibo,—another extraordinary form in which the forefinger is quite absent and the first toe armed with a long claw,—inhabits Old Calabar.