ei aileatal Omit iF} ty abatater ely insults ei taaslatela} para)riaiwiel se ? wi Pity taleiee ay Mahal 4 , iit Welty ae Maile) ‘ at « Vr telat Mahe ene 4 sPiseiny tid iy snes i sg ar tefl tis" 4 atta tien hte r SN a4) ae atte bitte cia} np *y? ieee te batt 4h TESthts agers AR rately 4 HI atdtes ae, aE FoR { tf tat * ae fra taeateltane itt ant shetty 4 ite eeley aie iy Athy een Bytes! ene. a dieyretith! A . Hity Pee ty ik basal ye! tiny , a mye y ie | Hh eile} é m . ‘ \, eA Puy paige / ' i / 2) ie eid Pare La a) . tae 1 aie (kl ee b a : Pattee ris os tu #5 ” ie f yeh ay Aidt itn ty ie 4¥4 EHR Pen yt lbh ahah hye 4 byt 4 + eG ‘ ~ ine er st tnbs ry ‘ Ment te ahaa ait} ebay ices Pain oi? Sy ieate i Ly pipe ui 4 ” Ais bat et sage can hid PU tth il peril : ey Bary ay Byite Ped * i yt But OU Terai sie fy! ah i oe i ryt ’ eet 4 mea . es “a AUSTRALIAN MUSEUM, SYDNEY CATALOGUE No. 16. CATALOGUE AUSTRALIAN MAMMALS GENERAL MAMMALOGY J. DOUGLAS OGIDEY, Fellow of the Linnean Society of London. PRINTED BY ORDER OF TIE TRUSTEES. E. P. RAMSAY, F.R.S.E., Curator. WITH INTRODUCTORY NOTES 1892. Foo ER RE a SERN ORE Re PP re lS Se ee eS es a | ne F. W. WHITH, PRINTER, MARKET SPRRET WEST., 733. AG3X Momeon. Oo ee MUSEUM, SYDNEY, CATALOGUE No. 16. CATALOGUE — OF AUSTRALIAN MAMMALS Z WITH INTRODUCTORY NOTES a ON Fellow of the Linnean Society of London. PRINTED BY ORDER OF THE TRUSTEES. E. P. RAMSAY, F.R.S.E., Curator. 1892. <9 Timid ailawal ‘ Ye “aL i a A ue i ra ) ierret May | 1 nn ; : ‘i eae 5 Juin ene tape é rs ae ; A >. py MeetAly ty pei: AB). PREFACE. Mr. J. Dovetas Ocitey having been engaged by the Trustees of the Australian Museum to prepare a Catalogue of the Aus- tralian Mammals, the work now issued is the result. It contains careful descriptions of all known Mammals indigenous to Australia, with notes also on allied fossil forms, compiled from various sources of which the author gives due acknowledgment in his Introduction. Nearly all the species are represented by one or more specimens in the Museum, and those which are not so are indicated by an asterisk placed against their names in the Index. Mr. Ogilby has found it necessary to alter many of the generally recognised names, for reasons which he gives in each case, consequently some of the specimens exhibited in the Museum may not bear the same designation as in the Catalogue. These differences will, however, ‘be remedied on the labels as speedily as possible. E. P. Ramsay. December, 1892. Oa Seep iy ES PAGE Introduction ove See ree ae ar Ae we Sena ua General Introduction to Mammals __... ies cae iss sea Pie Prototheria ... Metatheria ... wis 60: Aue ive Soc bo on nee 4 EKutheria ... sec a sb aD Sab ae ae aa 00) Sirenia a ace ste See ee acs Ses ne soar (Os Cetacea ace oye 56 ne 36 sec ids Boe ween om Chiroptera ... a eae és 5.6 ae MiG sae een Rodentia ... 506 aes ies eee 56C as wae ago. GE Carnivora ... ses wee ae ae S0C sae ae bo UP Index sce bk aoe coe S06 sce Sc siee amlok Bist OF WOOD cu TS. FIG. PAGE 1. Lower jaw of Dasyurus viverrinus ... SoC b6t nee ny LG 2. Side view of skull of Phascolarctos cinereus es ocr Aer At, 8. Side view of skull of Bettongia gaimardi ... ace Pas per ee 4, Under surface of skull of Hydromys chrysogaster, showing palate and dentition ; 4a. Upper molars enlarged ; 4b. Side view of same ... Bac aes 0 ee sec boc aoe LO 5. Side view of skull of same ... oes ree Bee ee sae LOL 6. Lower jaw of same... re oie Ges eed oa ee 101 eine Pe ae ront-ctet “ie PB i utens Nyaa Lina Na -) Lal egty rit Sinn UA bak Pte [2 ery Tt = heh a Rt rene gh, Dak st rg ih uM Rb Ms oe be BS iat Coy Boroaeeets «ssionasoaite (tad bene’ Bae Die AN ane La tier nigavic eel os Live api YS: aCe OEE Bert wiht?! by: cine Na Lan, sehen gin ae Ar | mee: we ; ‘f ; ie Ni nt, a ‘a aie St bl INTRODUCTION. ’ Tue “Handlist,” here submitted to the public, has been compiled more for the use of students and collectors than for scientists, for whom it contains little that is new or of special interest ; but it is believed that it will prove helpful, to the student in his earlier endeavors to unravel the mysteries of Nature, and to the collector that it may enable him, round his camp fire in the evening, to determine the specimens which he has obtained during the day. There are, however, besides the student and the collector, scattered over the length and breadth of these Colonies hundreds of educated men, chiefly of the medical profession, who, with all the thirst for research which the study of that profession necessarily engenders, are unable, except at rare intervals, to consult the numerous works which are now indispensable to its comprehension ; to these also it is hoped that these pages will prove of assistance by bringing, in however imperfect a manner, the history of Australian Mammalogy up to date, and thus supplying a much needed want. To all I trust that the short introductory notice on mammalian Osteology may be of value, but especially to collectors, on whom the author would wish to impress the imperative necessity of conserving the skeletons, even to the very smallest bone—those of the wrist and the ankle, and the so-called “ marsupial bones” should be specially looked after—of all Mammals obtained. To all, again and again, I must impress the fact that, however beautiful or strange the outside covering of the body may be, _ the skeleton is of infinitely more value to science; and not to the mammalogist alone but to everyone who sincerely endeavors to com- prehend the relationship between the various Families, Orders, and Classes of living creatures with which our earth is peopled. Since the publication of Mr. Gerard Krefft’s “Australian Verte- brata—Fossil and Recent,” published in the Catalogue Nat. Industrial Prods. N.S. Wales (1877), no work dealing systemati- cally with Australian Mammalogy as a whole has been attempted. In Mr. Krefft’s list 174 recent species are catalogued as against viii. 209 species and 8 well marked varieties in the present list, but several of those entered in the former list as good species, or at least as good species with a query, are here treated as varieties or synonyms of other species. Tf this little work should in any degree draw the attention of some at least of those who are fortunate enough to live in the country districts, to the extraordinary richness and the marvellous forms of mammalian life, of which the land of their birth or their adoption is the home, the author’s aspirations will have been amply fulfilled. With two of the Orders of the Eutherian Mammals, the CeracEa and the Ropent1A, the want of material and of works of reference, and, more especially among the J/uride, the multiplication of species and the number of species insufficiently described, have made the task exceptionally difficult, and the author, therefore, trusts that any shortcomings in these Orders will be leniently dealt with. The work has been compiled from various sources, the chief of which are the British Museum Catalogues of Messrs. Thomas, Dobson, and Gray, the different articles relating to Mammals in the Encyclopedia Britannica, especially that under the heading “MamMALIA” by Professor Flower; but numerous other works and papers by the same authors, as well as by Owen, Huxley, Mivart, Allen, Scott, Stirling, and others have been consulted and freely drawn from. In conclusion, I have to tender my best thanks to many friends, in Zoology chiefly to Dr. Ramsay, and in Paleontology to Mr. R. Etheridge, Junr., for valuable hints received and acted on. J. Douauas OGILBY. Class_-MAMMALIA. GENERAL INTRODUCTION. Mammals are the most highly organized forms of vertebrate animals, and may conveniently be defined as follows :— Warm-blooded animals, having the heart divided into four cavities, two auricles and two ventricles, and with a complete double circulation ; having the lungs separated from the abdomen by a complete muscular partition, termed the diaphragm ; having the skin more or less clothed with hair in its different modifi- cations; and with the young produced alive (except in the case of the very few aberrant forms, which constitute the Monotremes or PRoToTHERIA, see p. 1), and nourished for some time after birth by means of the mammary glands with which the female is provided. Limbs.—In the majority of Mammals the two pairs of limbs are well developed, and specially adapted for progression on the surface of the earth, but they are, in many cases modified to suit the re- quirements of the particular mode of life to which each individual genus has become habituated. For instance :—in some the fore limbs are specially formed for burrowing, as in the Wombat and Mole ; in others for climbing, as in the Opossums and Monkeys ; in others for flying, as in the Bats; and in others again for swimming, as in the Seals and Whales, in which case the hind limbs are rudimentary or more often entirely suppressed. Tail.—Most Mammals are provided with a tail, which, however, may be rudimentary, and therefore functionless, as is the case with the Koala, the Ape, the Deer, and many other genera ; prehensile, or formed for grasping, as with the American Opossums, the Cuscus, and certain families of Monkeys ; or fluke-like and so formed for rapid motion through water, as with the Whales and Dolphins. TEGUMENTARY STRUCTURES. Epidermis.—Almost all Mammals are clothed, and in the majority of cases thickly clothed, with a peculiarly modified form of the outer skin, or epiderm, variously known as hair, fur, wool, etc., which has its root at the bottom of a cavity in the derm or true skin. This substance assumes various forms, and is of various sizes and degrees of rigidity, from the soft fur of our Flying Squirrels to the spines of the Echidnas. The obvious purpose of this covering is to protect the skin against external influences, such as cold and damp, and in some cases against the x. attacks of enemies. On the Pangolins (Manide) of Africa and southern Asia alone, true imbricated scales, for the protection of the body, are present; between which, however, isolated hairs occur. Similarly imbricated epidermal productions are also found on the tails of many Rodents, such as the Beaver and the Rat ; of some Insectivores, such as Myogale ; and of some Marsupials, such as the Didelphyide ; among these Groups, however, these scales are frequently confined to the under surface of the tail. Only the Armadillos of South America possess a true bony exo- skeleton (somewhat similar to that of the Tortoises), which is covered with scutes of horny epiderm, and which is eminently fitted for defence against all ordinary enemies. The horns of the Ruminants and Rhinoceroses are also modified forms of epidermis, as also are nails, claws, and hoofs, and the perforated spur of the Monotremes. DENTAL SYSTEM. Dentition.—In all mammals, except the Narwhal, the teeth of the opposite sides of each jaw are alike in number and character. There are two distinct forms of dentition, the Homodont and the Heterodont ; the former, of which the Dolphins are the best exemplars, being, as its name implies, the more simple; in these the crowns are single-pointed and slightly curved, the roots also single and tapering, and all of similar formation, those in the middle of the series being, however, as a rule longer than those at either extremity. In the Heterodont dentition, on the contrary, the teeth are of different forms; the front teeth, or Incisors, are simple and one-rooted, and are adapted for cutting and seizing, while the back teeth, or Molars, have tuberculated or ridged crowns, are supported by two or more roots, and are specially formed for crushing and grinding the food ; between these two series there is frequently a longer and more sharply pointed tooth, popularly known as the “‘eye-tooth,” and technically—on aceount of its having attained to its highest development in the Wolves and their allies (Canide )—termed the Canine. By a similar process of development, though under widely different circumstances, the Marsupial Wolf or Tiger of Tasmania (Thylacinus/ has arrived at a precisely similar tooth ; the use of the canines is principally the tearing of the flesh of their victims and the holding of struggling prey. The molariform series is divisible into two parts, such of the posterior teeth as are without milk-predecessors being termed * Molars,” such as have milk-predecessors ‘“ Premolars.” In the Eutherian Mammals this series is generally constituted of four premolars and three molars, with a milk dentition normally con- sisting of three, the last premolar having invariably a predecessor ; but among the Marsupials this order is reversed in the permanent teeth, the number of premolars being one less and of molars one more, while the milk dentition, if present, is limited to a single xi. tooth on either side of each jaw, which is the predecessor of the third and last pre-molar. Only in the Anteaters (Myrmeco- phagide ), the Pangolins (Manidw), and the Echidna, are teeth entirely absent at al/ stages of growth. SKELETON. Skeleton.—The skeleton may be briefly defined as that portion - of the body of vertebrate animals which forms the framework on which the muscles are supported. In the adult state the greater part of this framework consists of osseous tissue, or bone, the remainder being cartilage. Bone is mainly built up on a gelatinous basis, strongly impregnated with salts of lime, chiefly phosphate. After the teeth, the bones are the most imperishable of al] the organs of the body, and are, therefore, of great value in affording reliable means of affixing the aftinities of extinct with recent forms. The skeleton is divided into two parts, the axial, consisting of the skull and vertebral column, and the appendicular, pertaining to the limbs. Skull.—In the skull, or cranium, of adult Mammals, all the bones, with the exceptions of the lower jaw, the auditory ossicles, and the bones of the hyoid arch, are immovably articulated together. The cranium, thus formed of numerous originally independent ossifications, consists of a brain-case for the enclosure and protection of that organ, and a face for the support of the organs of sight, smell, taste, mastication, defence, and offence. The brain-case articulates directly with the first cervical vertebra by means of a pair of oval prominences, called condyles, placed on each side of the large median foramen, which transmits the spinal cord; this method of articulation is termed dicondylian, and is only present in one other class of Vertebrate Animals, the BaTrRACcHIA, and this, together with several other characters, com- mon to these classes only, has given authority to the apparently well-founded assertion of the remote common origin of the Mam- malian and Batrachian types. Vertebre.—The vertebral column consists of a series of distinct bones, called “vertebre,” arranged in close connection with one another along the dorsal aspect of the body in the median line, and extending from the posterior margin of the cranium (to which it is firmly articulated) to the tip of the tail. The number of distinct bones varies greatly, principally owing to the elongation, or other- wise, of that appendage. In the mammalian vertebre the ends of the centra are usually flattened, but in the cervical region of some UncuxatTa certain of the vertebre may be opisthoccelous, that is having the hinder surface concave. The vertebral column is for convenience divided into five regions, cervical, dorsal, lumbar, sacral, and caudal. Cervical.—The cervical region forms the anterior portion of the column, and its first vertebra, called the atlas, articulates Xil. with the occipital region of the cranium ; these vertebre con stitute the framework of the neck, and in all known recent Mammals, except three—the Manatee (Manatus australis), the Two-toed Sloth ( Cholepus hoffmanni) with six, and the Three-toed Sloth (Bradypus tridactylus/ with nine—consists of seven distinct bones, which, however, are in the case of several genera, notably belonging to the Cetacea, in a greater or less number ankylosed together so as to form a solid mass. The second cervical vertebra is termed the amis, and, except in certain CETACEANS, always de- velops a well defined odontoid process. Dorsal, or Thoracic.—Behind these lie the dorsal, or, since to its vertebre only are articulated the movable ribs which form the arch of the thorax, as it would be more correct to term it, thoracic region; the anterior rib is attached below to the sternum (vide infra), as are also usually several of those which follow. Lumbar.—The lumbar region consists of those vertebree in front of the sacrum which bear xo movable ribs. The number of vertebrz in the conjoined thoracic and lumbar regions is tolerably constant in any given group of animals, any increase of the one being at the expense of the other; the smallest number of thoracico-lumbar vertebre occurs in the Armadillos (/ Dasypodide ) which have only fourteen, while the greatest number is found in the Hyrax or Rock-Rabbit, the supposed Cony of the Scriptures, in which no less than thirty are present; in Man, the higher Apes, and most Bats, the number is seventeen; in nearly all Marsupials, nineteen. Sacral.—The sacral region is that which is situated between the lumbar and caudal regions; in it the vertebre are ankylosed together so as to form a single mass ; the number of vertebre included in the sacrum is variable, even in different individuals belonging to the same species, especially as age advances, when certain of the caudal vertebree become incorporated with those of the true sacrum. ‘These bones are absent in the CETACEA. Caudal.—The caudal vertebree are those placed behind the sacrum, and terminate the vertebral column. They naturally vary greatly in number, there being usually four only in Man, and those rudimentary, whereas in the West African Long-tailed Pangolin (Manis longicaudata) there are as many as forty-six. They are also, for obvious reasons, numerous and highly developed in the Macropodide and the CETACEA. Chevron Bones.—To the under-surface of the caudal vertebre of many Mammals, in which the tail is well developed, are attached by articulation small bones, of the shape of an inverted arch, which have received the name of “ chevron bones.” Sternum.—The mammalian breast-bone (sternum) is a bone, or series of bones, placed longitudinally in the mesial line, on the inferior aspect of the thorax, and connected with the vertebral column by a series of more or less ossified ribs. It is divided xiii. into three portions, the anterior segment or presternwm, the posterior or xiphisternum, and a varying number between the two called the mesosternum. In the Whalebone Whales ( Balenide) only the presternum, supporting a single pair of ribs, is developed. ftibs.—The ribs form a series of long, narrow, more or less flattened bones, extending laterally from the sides of the vertebral column and mostly joined directly or indirectly to the sternum. Those which articulate directly are known as “true” ribs, and always belong to the anterior portion of the series, while the posterior ribs, which are either attached each to the edge of its preceding rib, or are free, are called, in the former case “ false,” in the latter, “floating” ribs. The portion of each rib nearest to the sternum is usually imperfectly ossified or permanently cartilaginous, and such parts are termed the “costal cartilages” ; in the rare cases in which they are completely ossified, as in the Armadilios, they are known as “sternal ribs.” Appendicular Skeleton.—The appendicular portion of the frame- work consists, when fully developed, of two pairs of limbs, an anterior and a posterior. Anterior Limb.—The anterior limb is present and fully de- veloped in all Mammals, and is composed of a shoulder-girdle and three segments of the limb proper, the upper arm /brachiwm ), the fore-arm (antibrachium ), and the hand (manus ). Shoulder-girdle.—The shoulder girdle is in most Mammals in a modified condition, compared with that in which it exists among the four remaining classes of Vertebrate Animals. In all Mammals, except the Monotremes—in which it is complete and articulated with the sternum—the coracoid is only present in the form of a process or even minute tubercle. The blade-bone (scapula) is always well developed, has a ridge on its outer surface—the so-called spine of the scapula—which generally terminates exter- nally in a free curved process called the ‘‘acromion.” The form of the scapula and the development of its processes largely depends on the uses to which the limb is put, for instance whether it be for burrowing, climbing, swimming, or merely for the support of the body. The collar-bone (clavicle), an accessary bar which connects the scapula with the sternum, may be present, asin Man and all Marsupials, except the Bandicoots ( Peramelide/; rudimentary and floating free in the flesh, as in the Dog, Cat, é&e.; or entirely absent, as in Seals, Whales, Ungulates, ce. Brachium and Antibrachiwm.—The proximal segment of the limb consists of a single bone, the hwmerus, and the second segment of two bones, the radiws and ulna, placed side by side, and articulating with the humerus at their proximal, and with the carpus at their distal extremities. In most Mammals these bones cross each other, the radius in front of the ulna, so that the former, though—nominally in vertebrates—external at the upper end is internal at the lower. In the majority of Mammals the Xiv. bones are fixed in this position, but in a few, as in Man, a free movement of crossing and uncrossing—technically known as pro- nation and supination—is allowed. In most Quadrupeds the ulna is much reduced in size, and the radius, especially at its upper end, correspondingly increased, so that the articular surface of the latter extends across the entire anterior surface of the humerus, and thus the bones become anterior and _ posterior, instead of external and internal. Manus.—The skeleton of the terminal section of the anterior limb consists of three divisions :—(1) the carpus, a group of small, more or less rounded or angular bones, with flattened surfaces contiguous to one another, which, though articulating by synovial joints, that is joints enclosing a capsule which secretes a lubricating fluid, have, nevertheless, scarcely any motion between them; (2) the metacarpus, a series of bones, placed side by side, and with their proximal ends articulating by almost immovable joints with the carpus; and (3) the phalanges, or bones of the digits proper, which are usually three in number to each digit, and articulate to one another, and the first to the distal end of the corresponding metacarpal bone, by freely movable hinge- joints. Carpus.—The mammalian carpus consists of two transverse series of bones, of which the upper or proximal, series contains three bones, that on the radial side, from which side all these bones are counted, being known as the scaphoid, that in the middle the /unar, and that on the left the cuneiform bone; the lower or distal series contains five bones, of which the two outer are always united into a single bone, and receive a common name; these have been respectively termed the trapezium, trapezoid, magnum, and unciform; between these two series a single bone, the central, may or may not be present. ‘Two additional bones are generally developed in the tendons of the flexor muscles, one on each side of the carpus, which may be called the radial and ulna sesamoid bones ; the latter of these, which is the more constant, and generally the larger, has received the distinctive title of the pisiform bone. Metacarpus and Phalanges.—The metacarpal bones are never more than five in number, nor are the digits which they assist in supporting ; they are described numerically as first, second, ete. The digits have each a distinguishing name, the poles (thumb), index, medius, annulus, and minimus. One or more of these may be in a rudimentary condition, or altogether suppressed, and where only one is absent it is generally the pollex. No Mammals, except the Ceracna, have more than three phalanges to each digit, while in the pollex one of the three is constantl absent. The terminal phalanges are usually specially modified to support the nail, claw, or hoof, and are termed wngual phalanges. Distinguishing terms are applied to the mode of XV. progression employed by various quadrupeds, according to the amount of palmar and plantar surfaces in contact with the ground; thus those, as the Bears, which use the whole of the lower surface of the carpus, metacarpus, and phalanges, are termed “plantigrade”; those, as the Horse, which apply the distal surface of the ungual phalanx and the horny structures surrounding it, “‘ wnguligrade”; intermediate forms exist, such as “nhalangigrade” for the Camel, and “subplantigrade” for most Carnivores. In the Bats the digits are enormously elongated for the purpose of supporting a cutaneous expansion constituting the organs of flight ; while in the Whales and Dolphins the manus is formed into a paddle, covered by continuous integument, and without any trace of nails or claws, and the number of phalanges belonging to the second and third digits always exceeds the normal number in Mammals, and sometimes very considerably. Posterior limb.—The posterior limb consists of a pelvic girdle, and three segments belonging to the limb. proper, the thigh (femur), the leg (tibia and fibula), and the foot (pes). Pelvic girdle.—The pelvic girdle is present in some form in all Mammals, but in the Sirenians and Cetaceans it is in a very rudimentary condition. Hach half of this girdle consists of three bones, which in the adult state are ankylosed together into a solid mass, and the single bone thus formed is technically known as the “os innominatum.” Of the three sections of which this bone is composed, the upper (z/iwm) is firmly articulated to the sacrum, and of the two lower, the antero-inferior (pubis) forms a symphysis with its fellow of the opposite side, except in the Insectivorous genera, Soricide, Talpide, and Chrysochloride, where these bones are entirely separated, while the postero- inferior /ischiwm) are never united. These three sections unite around a cup-shaped cavity, the acetabulum, into which the proximal end of the femur is received. Between the pubis and ischium there is a large opening known as the “‘obtwrator foramen.” The two innominate bones, in conjunction with the sacral, form the pelvis. By this direct articulation of the innominate bones with the vertebral column, greater strength is given to the hind limbs to increase their powers of supporting and propeling the body. In the Monotremes and Marsupials an additional pair of thin, flat, elongated bones, called the “ epipubie” or “marsupial” bones, the exact function of which is but im- perfectly understood, is attached to the fore part of the pubis, and projects forward into the muscular wall of the abdomen. Thigh and Ley.—As with the fore-limb, the proximal segment of the hind limb has but one bone, the femur, and the second two, the tibiw and the fibula ; these lie parallel to one another, the former, which is much the more strongly developed being on the inner side and more to the front, while the latter is on the outer side and behind. They are never either permanently XVi. crossed or capable of any considerable amount of rotation, as in the corresponding bones of the antibrachium. In many Mammals the fibula is rudimentary, and in some, as certain ruminants, it forms, in old animals, a more or less complete ankylosis with the tibia. A large sesamoid bone, known as the knee-cap or “‘patella,” is developed in the tendon of the extensor muscle of the thigh, in front of and for the protection of the knee-joint, and is present in an ossified condition in all Mammals, excepting some of the Marsupials. Foot.—The terminal segment of the hind limb, like that of the fore limb, consists of three parts, of which the proximal is termed the tarsus, the median the metatarsus, and the distal the phalanges. In the tarsus the proximal series always consists of two bones, the astra/agus, representing the coalesced scaphoid and lunar of the hand, and the ca/ecaneum. The former is placed more to the dorsal side of the foot, and almost exclusively furnishes the tarsal portion of the ankle joint; the latter is situated more towards the plantar side of the foot, and is elongated backwards to form a more or less prominent tuberosity (the heel) to which the tendon of the great extensor muscles of the foot is attached. The navicular bone is interposed between the proximal and distal series on the inner side of the foot, thus leaving the two series in contact on the outer side. The distal series, when complete, contains four bones, which, beginning as usual on the inner side, are the three cuneiform, the internal being known as the first or ento-cuneiform, the median as the second or meso-cuneiform, and the external as the third or ecto- cuneiform ,; of these the second is the smallest, and all three are articulated to the distal surface of the navicular ; the fourth bone is the cuboid, and articulates with the calcaneum; in Mammals where the hallux is wanting, the ento-cuneiform may be rudi- mentary or altogether absent. The three cuneiform bones support the first, second, and third metatarsal bones, and the cuboid the fourth and fifth ; as in the hand sesamozd bones are developed in addition to the constant bones of the tarsus. The formation of the phalanges of the foot is in all respects similar to that of the hand, and, with the one exception of the inner digit—which is termed the hallux, and corresponds to the pollex of the hand— the names applied to the other digits of the foot are the same as those by which the corresponding digits of the hand are known. In the hallux, as in the pollex, one bone of the normal mamma- lian four—including the metacarpals and metatarsals—is wanting, and it is still a disputed question whether the missing bone is the first metatarsal, or the proximal phalanx. In the Srrenra and Ceracea no traces of the third or distal segment of the hind limb have been discovered, and only in certain members of the 1]: tter Order have even rudiments of the proximal and median segments been detected. Subclass I—PROTOTHERIA. The MonoTrREMATA or ORNITHODELPHIA, as the Prototherian Mammals have been variously, and more or less misleadingly termed, comprise the lowest, and in point of time the most ancient, types of mammalian life. Two families only, consisting of three genera, exist at the present time, the extent of their range being confined to Australia and Tasmania ( Ornithorhynchus and Echidna) and New Guinea (Proechidna and Echidna). They are oviparous, and the young are nourished after emerging from the egg by milk expressed from the mammary glands into a temporary pouch ; these glands are not provided with nipples, the milk being forced out through numerous apertures in the spongy skin. The method employed in hatching out the eggs differs materially in the two families, for while the Platypus forms a nest in its burrow on which to deposit its eggs, and hatches them out by the warmth of its body in the same manner as birds do,—the pouch being at no time sufficiently developed to enable the animal to retain the eggs therein—the Echidna carries its eggs about with it and hatches them out in its more highly specialized pouch. The males are provided with a perforated spur on the inside of the heel, which is connected by a duct with a postfemoral gland, and the functions of which are not as yet clearly understood; the assumption that it is a poison-organ is not however borne out by actual evidence, while on the contrary it is difficult to imagine of what possible value such an organ could be to animals so consti- tuted ; it is, however, possible that it may develop such a function in a greater or less degree during the breeding season, and be used as a weapon of defence in contesting for the favor of the femaies. The Monotremes possess an additional clavicular bone, in the shape of a large T-shaped interclavicle, which bone is not represented in either of the other mammalian Subclasses ; the coracoid bone is complete and articulates with the sternum. Epipubic bones are present. True functional teeth are absent in the adults. Order I.-—MONOTREMATA. Muzzle produced into a beak, which is either flattened or cylindrical. External ear-opening without a conch, Limbs sub- equal in length, short and powerful. Tail either short and broad or rudimentary. Mamme rudimentary. A bo ORNITHORHYNCHIDA. Family I.—ORNITHORHYNCHID/. Muzzle in the shape of a broad, flattened, horny beak. Tongue not extensile. Fur not mixed with spines. Tail well developed, broad, and flattened. Hands and feet modified as swimming- organs, the toes broadly webbed. Palms and soles naked, without pads. Teeth rudimentary, only found in young animals, in which there are two on either side of the upper jaw and three on either side of the lower jaw, these being persistent till the animal is rather more than one-third grown ; never cutting the gum; multi- cuspid ; replaced in the adults by strong, horny plates. Cerebral hemispheres smooth. Genus I.—ORNITHORHYNCHUS, Blumenbach (1800). Form elongate and depressed. Toes 5—5, all with long claws, which on the fore feet are broad and blunt, on the hind feet compressed and pointed. Beak short, with a basal projecting leathery flap both above and below. Cheeks pouched. Vertebre.—C. 7, D. 17, L. 2, S. 2, Cd. 20 or 21 = 48 or 49. Habits.—Aquatic ; fossorial ; feeding on crustaceans, mollusks, water-insects, worms, ce. _Note.—Under the name of Ornithorhynchus agilis, Mr. C. W. De Vis has described (Proc. Roy. Soc. Queensland, 1885, p. 35, pl. iv.), from a right tibia and the distal half of a right mandible, what appears to be a very distinct species of fossil Platypus ; re- versing the general law in such cases, this extinct species, which from the dentition is unquestionably adult, must have been of a considerably smaller size than its living representative. The fossils were excavated on King’s Creek, an affluent of the Conda- mine River, near Pilton, South Queensland. Shaw’s name Platypus (1799) having been employed by Herbst six years previously for a genus of Coleopterous Insects is inadmissable. 1. ORNITHORHYNCHUS ANATINUS, Shav, sp. (1799). Duck-billed Platypus; Water Mole. Male much larger than female. Fur short, close, and velvety. General color above deep umber- or blackish-brown; below grayish-white ; a white or yellowish spot round the eye; tail colored above like the back, generally naked below ; bill black above, yellow and black below. Dimensions.—Head and body of male, about eighteen, of female about fourteen inches; tail of male about six, of female about five inches. Habitat.—Queensland southwards of 18° 8. lat., New South Wales, Victoria, South Australia, and Tasmania. Aa ECHIDNA. 3 References.—Thomas, B. M. Catal. p. 388; Gould, Mamm. Austr. i. pl. i. Famly I1.—ECHIDNID. Muzzle in the shape of a slender cylindrical beak. Tongue extensile. Fur mixed with stout spines. Tailrudimentary. Toes not webbed. Palms and soles forming broad, fleshy cushions, without distinct pads. Teeth wholly absent, without functional successors. Palate and tongue spinous. Cerebral hemispheres convoluted. Genus I.—ECHIDNA, G@. Cuvier (1798). Form stout and depressed. Toes 55, all clawed, those on the fore feet broad, but little curved, and directed forwards ; on the hind feet slenderer, curved outwards, the second, or second and third, very long, much exceeding the fourth and fifth; that of hallux short, blunt, and rounded. Beak straight or with a slight upward curve. Tongue tapering at the tip, the spines restricted to the basal portion. Vertebree.—C. 7, D. 16, L. 3, 8. 3, Cd. 12=41. Habits.—Terrestrial ; fossorial ; feeding chiefly on ants and their eggs. Note.—In 1868 Mr. Gerard Krefft described (Ann. Nat. Hist. (4) i. p. 113) from a fragment of a humerus a fossil species from New South Wales, for which he proposed the name Lchidna oweni; subsequently numerous examples were obtained from the Welling- ton Caves, N.S.W., and were separated from the original species by Prof. Owen under the name of #. ramsayi. Paleontologists now, however, seem to be agreed that the two forms are identical. 1. Ecurpna acuLeata, Shaw, sp. (1792). Common Echidna; Native Porcupine. Sexes not markedly differing in size. General color of hair above black or dark brown; below brown. Spines of back long and stout, generally quite hiding the hair, their color normally yellow with a black tip. Tail short and conical, terminally naked. Several different species of Echidna have been described, but recent researches tend to prove that these are at best but geo- graphical races. The Port Moresby variety (2. lawesi, Ramsay) the type of which is in the Australian Museum, Sydney, differs in its smaller size and shorter dorsal spines; the Tasmanian variety (H. setosa, E. Geoffroy) in its larger size, longer hair which almost conceals the spines, and the much longer third claw of the hind feet, which almost equals the second claw. 4 METATHERIA, Dimensions.—Head and body, £. lawesi, about fourteen inches; E. aculeata, about seventeen, and £. sefosa about twenty. Habitat.—From South-eastern New Guinea throughout the whole of Australia to Tasmania. References.—Thomas, B. M. Catal. p. 377; Gould, Mamm., Austr. i. pls. ii. (#. aculeata), ii. (£. setosa ). Subclass II—METATHERIA. The Metatherian Mammals, more generally known as the DipELPHtIA or MARSUPIALIA, are at the present time, with the ex- ception of the True Opossums (Didelphyide) of the New World, confined to the Australian, Papuasian, and the eastern islands of the Austro-Malayan subregions ; the easternmost point to which their range extends being the Island of San Christoval, belonging to the western section of the Solomon Archipelago, where the short- headed variety of the Gray Cuscus (Phalanger orientalis var. breviceps) is found ; the Group was however at a former period much more generally distributed over the surface of the earth, species having been discovered in a fossil state in Europe, South Africa, and America. They differ from all other Mammals by the presence in the female of a permanent pouch (marsuprum)— obsolete in Myrmecobius and practically so in Phascologale— formed by a fold in the integument, and which is furnished with a varying number of teats, to which the young are attached at a very early stage of growth by the mother, who, by means of specially adapted muscles, forces the milk from the mamme into their mouths, their condition being for a considerable period so imperfect as to preclude the possibility of their obtaining nutri- ment of their own volition. Both sexes are provided with long epipubic bones, generally known as “marsupial bones,” though having in reality no connection whatever with the pouch; these bones are rudimentary in Zhylacinus, while in the Bandicoots (Peramelide) the clavicles are wanting. Order I.—MARSUPIALIA. Limbs subequal, or the hinder pair much the larger and form- ing the chief agents in progression. Tail almost invariably present, generally long, and often prehensile. Teeth very variable in structure. Mamme in varying numbers. Suborder I.—Polyprotodontia. Incisors numerous, four or five in the upper, three or four in the lower jaw, subequal, much smaller than the canines. Molars generally sharply cuspidate. Habits.—Carnivorous ; insectivorous ; rarely omnivorous. NOTORYCTES. 5 Family IL—NOTORYCTIDA. Limbs subequal, short, and very strong. Fore feet with five digits ; hind feet asyndactylous, with five toes ; hallux clawed; the other toes unequal in size. No visible external eyes. Ears without conch. Clavicle well developed. Chevron bones present. Genus I.—NOTORYCTES, Stirling (1891). Dorsal aspect of snout covered by a hard horny shield, which is divided into two segments by a transverse ridge. Mouth ven- tral in position. Ear openings present, but almost completely concealed by the overhanging fur. Tail hard, tough, and leathery, marked by conspicuous annular rings, thick at its insertion but rapidly decreasing in size towards its extremity, which is blunt and knob-like. The four inner toes of both fore and hind feet clawed, the fifth with a short, broad, horny nail. Palms and soles naked, covered with tough, leathery, wrinkled skin ; the latter traversed by oblique folds. The claws of the third and fourth digits enormously developed; those of the corresponding toes curved outwards and backwards. Pouch opening backwards. Mamme two, minute. Vertebrae.—C. 7, 1). 15, L, 4, 8. 6. C. 12 = 44. *)° 1.2.3.4 0 1.0.3.4 1.2.3.4 a 9 Dentition.—I. 23 C. 0 P; 1.0.3.40r0? M. 1234 x s4= 40 to 42. Habits.—Terrestrial ; fossorial ; insectivorous. Note.—The axis and four succeeding cervical vertebre are firmly ankylosed together, as are also all the sacral vertebre. In the dental formula given above I have preferred to consider the teeth, which Dr. Stirling figures as an upper and lower canine, as a fourth upper and third lower incisor. 1. Notorycres TyPHLOPS, Stirling (1888). Marsupial Mole. Size small, form stout. Fur long, soft, of a bright lustrous silken appearance ; sometimes darker across the loins ; a patch of darkish red fur surrounding the pouch ; interior of pouch sparsely lined with reddish fawn-colored hairs. Upper surface of tail clothed with fur similar to that of the back on its anterior half; the sides and lower surface naked. Dimensions.—Head and body about five inches ; tail about one and one-fifth inch. Habitat.—Central South Australia. References,—Stirling, Trans. Roy. Soc. South Austr. 1888, p. 21, and 1891, p. 154, pls. ii. — ix. Note.—In the attempt to formulate the above divisional and generic definitions for Dr. Stirling’s Motoryctes typhlops, I have 6 NOTORYCTES. experienced considerable difficulty in the selection of such char- acters as appear to be most suitable for the purpose. Dr. Stirling, in his papers quoted above, though at present the only scientist who has had the opportunity of examining the anatomical charac- ters, offers no suggestion as to the definite place which it should take in the zoological system, and I have therefore endeavored to intercalate it among those forms to which it seems to me to make the nearest approach from a structural point of view. The con- clusion at which I have arrived, after an exhaustive study of Dr. Stirling’s pamphlet, is that in this animal we have at last obtained a definite connecting link between the Monotremes and Marsupials. In the present initial state of our knowledge it would, in my judgment, be presumptuous to class otoryctes among the Monotremes proper, nevertheless several of our leading naturalists incline to the opinion that its affinities are closer to these Mammals than to the Marsupials; at present, however, I prefer to look upon it as an aberrant Polyprotodont. If the former view be correct we have here an adult Monotreme possess- ing fully developed teeth, and it must not be lost sight of that in Ornithorhynchus, as previously mentioned (vide p. 2), teeth are developed in both jaws until the animal is fully one-third grown, though our knowledge of the early life of this latter animal is not sufficient to enable us to decide whether these teeth are functional or otherwise ; it is, however, on this character, and so far as I can determine with the slender means at my disposal, on this character alone, that I base my opinion of its polyprotodont affinities; the absence of canine teeth, if I am correct in my suggestion that those considered by Dr. Stirling to be canines are respectively the fourth upper and third lower incisors, militates against: its position as a typical Polyprotodont, but strengthens its position as a true connecting link between the Monorremata and Poty- PROTODONTIA; if on the other hand Dr. Stirling has taken the correct view of the nature of the teeth in question, my contention as to the polyprotodont character of Motoryctes is materially strengthened; in any case our knowledge is so limited, and our lack | of information as to its milk dentition, if any, so absolute, that it would not be wise to separate it from the polyprotodont Mammals. Further the semirudimentary nature of the pouch, which wholly, or at any rate partially, disappears when not in use, points to a connection on the one hand with Myrmecobius and Phascologale, and on the other hand with the Prorotueria ; Dr. Stirling informs me in literis that a pair of minute mammary elevations are present, situated near the corners of the posteriorly expanded pouch. The form of the feet and the character of the horny shield on the snout also ally Votoryctes to Echidna. Putting aside these external characters, we have not far to seek in the skeleton for contir- matory evidence of its affinity to the Monotremes, the considerable DASYURIDA. sf development of the clavicle, which is connected by a ligament to the sternal apparatus, along with the rudimentary character of the epipubic bones, being also monotrematous ; this latter character, however, it shares with the Dasyurine Thylacinus. Referring back to the clavicular development the fact must not be lost sight of that this bone is reduced to a mere knob-like process in the Dasyures and is entirely absent in the Bandicoots, while in the Monotremes it connects by true ossification with the sternum. It may be sought to explain away this difference in the strength of the shoulder-girdle on the grounds that Notoryctes, Echidna, and Ornithorhynchus have the fore limbs strengthened, in order to enable them to burrow with the greater ease, but the superficiality of such a view is demonstrable at a glance if we take into con- sideration the fact that the Peramelide, which are also of fossorial habits, though not in so marked a degree as the genera mentioned above, are absolutely without rudiments of these bones. The method of reproduction in Woforyctes is undeniably one of the most interesting problems of the day in the world of science, and when solved will at once set at rest the question of its affinities. It seems probable that, though so essentially a burrowing animal, Votoryctes does not live in a burrow, but makes a nest in tussocks of grass or at the roots of small shrubs, burrowing, like the Peramelide, for food only. Its method of progression is some- what analogous to that of a Dolphin as, according to Dr. Stirling’s informants, it travels for varying distances at very few inches beneath the surface, then emerging crawls along the surface for a few feet and again dives below ; this seems to be necessary to the act of respiration. As fast as it bores by means of the fore feet and horny snout it closes up the burrow behind it with its hind feet. Finally, should the theory above advanced prove correct, we have now obtained a definite link between the proto- and meta- therian Sub-classes—a link which is somewhat analogous in position to that held by Branchiostoma between the vertebrate and invertebrate animals—and which will perhaps eventually bridge over the gulf which at present separates the Monotremes from the Marsupials. It is, however, probable that it is to embryological and palzontological research alone that we must look for the elucidation of the problem briefly hinted at above. In a work of this kind it is impossible to go more fully into the subject of this interesting animal. Family I1.—DASYURIDL. Thylacine; Native Cats; Pouched Mice, &c. Limbs subequal. Fore feet with five digits; hind feet asyn- dactylous, with four’ or five toes; hallux small and clawless, or 8 MYRMECOBIINE. absent ; the other toes subequal. Stomach simple. Ccecum absent. Pouch, when present, opening forwards or downwards, sometimes rudimentary, rarely obsolete. Subfamily [.—Myrmecosun2. Tongue long, cylindrical, and extensile. Rhinarium naked, grooved below. Lower lip pointed, projecting beyond the teeth. Chest with a complex gland opening to the surface by several large and distinct apertures. Molars small and delicate, more than four in number in each ramus, those of the lower jaw with the inner cusps larger than the outer. Genus I—MYRMECOBIUS, Waterhouse (1836). Form graceful and squirrel-like. Ears long and narrow. Toes 5 — 4, provided with long fossorial claws; hallux absent externally. Palms naked, soles partially so; pads small and granulated. Tail long and bushy. Pouch obsolete. Mamme four (Zhomas), but Gilbert states (Gould, Mamm. Austr.) that he has ‘observed seven young attached to the nipples.” 1.2.3.4 1.0.3.4 1.2.3.4.5.0 Dentition.—I. 753) (eres eng ap oe aReeROe eS OU Eee Habits.—Terrestrial ; LebSreAl ; insectivorous. Note.—A fourth incisor is rarely present in the lower jaw. 1. Myrmecosius Fasciatus, Waterhouse (1836). Marsupial Anteater. Fur short, close, and hispid. General color above bright rufous, grizzled on the head, darkening posteriorly, where it is transversely banded with white; a white stripe over each eye ; below clear pale yellow. Ears pointed, clothed with close, short hairs, rufous behind, yellowish inside. Claws dark horn-color. Third finger shorter than second or fourth. Palms with five small, round, finely granulated pads ; soles hairy along the edges, with only three pads. Tail long-haired above, shorter-haired below; the former grizzled yellow and black, the latter rich rufous. Dimensions.—Head and body about ten inches; tail about seven inches. Habitat.—South and West Australia. References.—Thomas, B.M. Catal. p. 312, pl. xxiii. fig. 10 (sole ); Gould, Mamm. Austr. i. pl. iv. Note.—Mr. Thomas remarks :—The chief interest of this remarkable genus lies in its close resemblance and, presumably, relationship to the Mesozoic Polyprotodont Marsupials (Phascolo- theriwm, Amphilestes, &c.) of the English Jurassic beds, the resem- SMINTHOPSIS. 9 blance being so close as to suggest that Myrmecobius, like Ceratodus, is actually an unmodified survivor from Mesozoic times. Subfamily II.—Dasyvurina. Tongue short, simple, not extensile, Lower lip rounded, not produced. Chest without gland. Molars large, four in number in each ramus; those of the lower jaw with the outer cusps larger than the inner. Genus IIl.—ANTECHINOMYS, Aref (1866), Body unspotted. Ears very large. Tail very long, tufted. Limbs unusually elongated ; the fore-arm, lower leg, and hind foot disproportionately long. Toes short and subequal ; hallux absent. Palms and soles without distinct pads, the greater part of the latter hairy. Mamme? Canines very small. Dentition.—I. 7334, 0.3, Pe coaa, M. 34 x 2=46. Habits.—Terrestrial ; saltatory ; insectivorous. 1. ANTECHINOMYS LANIGER, Gould, sp. (1856). Wooly Pouched Mouse; Jerboa Pouched Mouse. Size small; form slender and graceful. Fur long, soft, and fine. General color above slaty gray ; below white; a fawn-colored patch behind the ear. Ears ovoid, almost entirely clothed with short, fawn-colored hairs. Lower part of limbs, hands, and feet white. Tail very long, slender, short-haired, fawn-colored except the terminal inch which is tufted and black. Dimensions.—Head and body about three and a half inches ; tail about five inches. Habitat.—Interior of New South Wales and Southern Queens- land References.—Thomas, B.M. Catal. p. 309, pls. xxiii. fig. 9 (sole), xxv. figs. 11 & 12 (skuli); Gould, Mamm. Austr. i. pl. xxxiii.; Alston, P.Z.S. 1880, p. 545, pl. xlv. Note.—Through want of information respecting its habits Gould’s figure represents a pair seated on the bough of a tree ; the figures also are very misleading. Genus III.—SMINTHOPSIS, Thomas (1887). Body unspotted. Form slender and delicate. Ears large and broad. Tail moderate or short, short-haired, sometimes incras- sated. Feet slender and delicate. Toes subequal, with small, delicate claws; hallux present, short and clawless. Soles partially 10 SMINTHOPSIS. hairy, the naked part granulated, with or without pads, which, when present, are not or but indistinctly striated. Pouch well developed. Mamme eight or ten. . 12.3.4 cy 1 LOSI” ug LOM Meee Dentition. II. 123? C. Su igh 1.0.3.4 M. 1.2.3.4 x 2= 46. Habits.—Verrestrial ; insectivorous. Note.—Gould’s name Podabrus (1845) cannot stand, having been previously (1840) bestowed upon a genus of Coleopterous Insects by Fischer. 1. SMINTHOPSIS CRASSICAUDATA, Gould, sp. (1844). Thick-tailed Pouched Mouse. Size small; form light and delicate. Fur very soft and fine. General color above clear ashy-gray ; below grayish-white ; chin white. Ears very large and rather pointed, their backs dark brown anteriorly, strongly contrasting with the lighter hues posteriorly. Hands and feet white. Greater part of soles clothed with velvety hairs; naked parts granulated, without distinct striated pads. Tail short, incrassated, tapering, gray above, white below. Mamme ten. Dimensions.—Head and body about three and a half inches ; tail about two inches. Habitat.—All Australia except the extreme North. References.—Thomas, B.M. Catal. p. 306, pls. xxiii. fig. 8 (sole ), xxv. fig. 10 (teeth); Gould, Mamm. Austr. i. pls. xlvi. GS. mac- rurus), xvii. (S. crassicaudata ). 2. SMINTHOPSIS MURINA, Waterhouse, sp. (1837). Common Pouched Mouse. Size small ; form very slender and delicate. Fur soft and fine. General color above finely grizzled mouse-gray; below grayish- white ; chin white. Ears very variable in size, their backs uni- formly slaty flesh-color. Hands, feet, and sometimes fore-arms white. Greater part of soles naked, finely granulated, without distinct striated pads. Tail moderate, slender, not incrassated, brown above, gray or white below. Mamme eight. Dimensions.—Head and body about three and a half inches ; tail about the same. Habitat.—Australia south of the tropics. References. —Thomas, B.M. Catal. p. 303, pl. xxiii. fig. 7 (sole ); Gould, Mamm. Austr. i. pls. xli. (S. fuliginosus ), xlii. (iS. albipes ), xii. (S. murinus). PHASCOLOGALE. ll 3. SMINTHOPSIS LEUCOPUS, Cray, sp. (1842). White-footed Pouched Mouse. Size medium; form slender. Fur close, fine, and straight. General color above uniform dark grayish-brown or mouse-color, with no prominent markings; below white. Ears large and broad, their backs uniform slaty-gray. Hands and feet pure white. Palms finely granulated, with six pads. Soles finely hairy posteriorly, coarsely granulated anteriorly ; the pads small, four in number, and finely striated transversely. Tail moderate, slender, shorter in southern than in extreme northern specimens, gray or brown above, white below. Mamme? Dimensions.—Head and body about four inches; tail in southern examples about three and a half, in northern about four inches, Habitat.—Eastern Australia from Cape York to Tasmania. References.—Thomas, B.M. Catal. p. 302, pls. xxiii. figs. 5 (ear ), 6 (sole), xxv. figs. 7 (teeth), 8 and 9 (skull); Gould, Mamm. Austr. i. pls. xxxv. (S. leucopus), xxxvi. (S. ferruginetfrons ). 4. SMINTHOPSIS VIRGINLE, De Tarragon, sp. (1847). Striped-faced Pouched Mouse. Size large. Fur rather short, very soft and silky. General color above grizzled gray; below white or pale yellow. Face sandy rufous, ornamented with a central and on each side a lateral black longitudinal line. Cheeks, sides of neck, and basal ear-tufts bright rufous. Ears very large and nearly naked. Outside of upper arms and thighs like the back; rest of limbs white. Sole-pads probably similar to those of S. Jewcopus. Tail short-haired, dark brown above, paler below. Mamme ? Dimensions.—Head and body about five inches ; tail about the same. Habitat.—Herbert River District, Queensland. References.—Thomas, B.M. Catal. p. 300; Collett, P.Z.S. 1886, p- 548, pl. lx. (animal, skull and teeth ). Genus [V.—PHASCOLOGALE, Zemmuinck (1827). Body unspotted. Form slender and graceful. Ears rounded. Tail long; bushy, crested, or nearly naked. Feet broad and short. Toes subequal, with sharp, curved claws ; hallux present, short and clawless. Soles naked, granulated, with five transversely- striated pads ; the hallucal pad often divided into two. Pouch practically obsolete. Mamme four, six, eight, or ten. +: 1.2.3.4 1 1.03.4 a er oe Dentition.—I. 123” (Se Dp Ps 1.0.3.2 M. i234 x 2= 46. Habits.—Arboreal ; insectivorous. Note.—The fourth premolar is absent in P. cristicaudata. 12 PHASCOLOGALE. 1. PHASCOLOGALE CALURA, Gould (1844). Lesser Brush-tailed Pouched Mouse. Size medium ; form slender. Fur long, soft, and fine. General color above gray with a faint rufous tinge; below white. Ears very large, almost naked, with well-marked basal tufts of red hair. Hands and feet white. Soles with five pads, the hallucal very long, but undivided ; claws small and weak. Tail long; the basal half short-haired, rufous above, dark brown below ; the terminal half black, and slightly bushy all round. Mamme? Dimensions.—Head and body about five inches ; tail about six inches. Habitat. South and West Australia. References.—Thomas, B.M. Catal. p. 296, pls. xxiv. fig. 9 (upper view of skull), xxv. fig. 6 (teeth); Gould, Mamm. Austr. i. pl. xxxii. 2. PHASCOLOGALE PENICILLATA, Shaw, sp. (1800). Greater Brush-tailed Pouched Mouse. Size large; form stout and strong. Fur short and coarse. General color above finely grizzled pale gray ; below, chin white, chest, belly, and innerside of limbs white or pale gray, the pouch- hairs dull rufous. Muzzle with an indistinct darker stripe. Ears very large, nearly naked. Feet and hands gray. Soles with the five primary pads very long, the hallucal pad undivided, and a minute supplementary pad posteriorly on the outer margin ; claws long and strong. Tail long and thick, the terminal half or three- fifths thickly clothed all round with long black hairs, forming a prominent brush. Mamme ten. Dimensions.—Head and body about ten inches; tail about nine inches. Habitat.—All Australia, except the extreme North. References. —Thomas, B.M. Catal. p. 294, pls. xxiii. fig. 4 (sole), xxiv. fig. 4 (teeth) ; Gould, Mamm. Austr. i. pl. xxxi. 3. PHASCOLOGALE MINUTISSIMA, Gould, sp. (1851). Pigmy Pouched Mouse. Size very small. Fur short, soft, and fine, mainly composed of underfur. General color above finely grizzled mouse-gray; below, chin white, chest and belly similar to, but paler than back. Ears of medium size, thinly clothed with short hairs. Hands and feet pale brown. Soles naked, with seven pads. Tail of moderate length, short-haired. Pouch fairly developed. Mamme eight. Dimensions.—Head and body about three inches; tail about two and a half inches. Habitat.—Central and Southern Queensland. PHASCOLOGALE. 13 References.—Thomas, B.M. Catal. p. 292, pls. xxiv. fig. 8 (upper view of skull), xxv. fig. 3 (teeth); Gould, Mamm. Austr. i. pls. xliv. (P. maculata), xlv. (P. minutissima ). 4, PHASCOLOGALE FLAVIPES, Waterhouse (1837). Yellow-footed Pouched Mouse. Size small or medium ; form stout. Fur close and rather crisp. General color above gray suffused with yellow or rufous; below yellow or rufous. ars rather large, naked above, their bases tufted externally with yellow or gray. Limbs and feet more or less like the belly. Soles naked, with six pads, the hallucal usually divided. Claws small and delicate. Tail short-haired, brown or yellow above, paler below, the terminal inch sometimes black. Mamme eight. Dimensions.—Head and body about five inches; tail about three and a half inches. Habitat.—From New Guinea throughout Eastern Australia to South Australia. References.—Thomas, B.M. Catal. p. 289, pl. xxv. fig. 5 (teeth); Gould, Mamm. Austr. i. pls. xl. (P. flavipes), xxxvii. (P. wnicolor). 4a, P. FLAVIPES var. LEUCOGASTER, Gray (1841) White-bellied Pouched Mouse. Differs from the typical form only in the underside and limbs being white. Habitat.—Northern and Western Australia. References.—Thomas, B. M. Catal. p. 291; Gould, Mamm. Austr. i. pl. xxxviil. 5. PHASCOLOGALE MINIMA, Geoffroy, sp. (1804). Little Pouched Mouse. Size medium ; form murine. Fur thick and close, but rather harsh. General color above gray, suffused with yellow or rufous, more strongly posteriorly ; below, chin white, chest and belly dirty yellowish-gray. Ears short, nearly naked, generally tufted at the base. A yellow patch on the front and outside of the hips. Hands and feet gray, yellow, or brown. Soles naked, with five pads, but the hallucal sometimes divided. Claws very long and strong. Tail short, closely short-haired, brown above, paler below. Mamme ? Dimensions.—Head and body about five and a half inches ; tail about three and a half inches. Habitat.—Tasmania and the adjoining Islands. References.—Thomas, B.M. Catal. p. 287. 14 PHASCOLOGALE. 6. PHASCOLOGALE SWAINSONI, Waterhouse (1840). Swainson’s Pouched Mouse. Size medium. Fur very long, soft, and thick. General color above deep rufous- or umber-brown, below dull brownish-gray. Muzzle long. Ears short and broad, covered with short dark brown hairs. Hands and feet dark brown. Soles with five pads, the hallucal not, or scarcely divided. Fore claws very long and strong. Tail moderate, short-haired, uniformly dark brown. Mamme probably ten. Dimensions.—Head and body about five inches; tail about four inches. Habitat.—Tasmania ; South-east Victoria, References.—Thomas, B.M. Catal. p. 285, pls. xxiv. fig. 7 (wpper view of skull), xxv. fig. 4 (teeth); Gould, Mamm. Austr. i. pl. xxxiv. 7. PHASCOLOGALE APICALIS, Gray, (1842). Freckled Pouched Mouse. Size medium. Fur coarse. General color above freckled reddish-gray; below dull white or yellowish. A whitish ring round the eye. Ears short and rounded, clothed inside and out- side with short gray hairs. Front and outside of fore-arm rufous; rest of outsides of limbs dull gray. Hands and feet gray. Soles granulated ; hallucal pad rarely subdivided. Tail short, hairy, colored above like the back, below gray or yellowish-gray ; the extreme tip black. Mamme eight. Dimensions.—Head and body about five inches; tail about three and a half inches. Habitat.—West and probably North Australia. References.—Thomas, B.M. Catal. p. 277, pls. xxiv. fig. 5 (upper view of skull), xxv. fig. 1 (teeth); Gould, Mamm. Austr. i. pl. xxxix, 8. PHASCOLOGALE CRISTICAUDATA, Krefft, sp. (1866). Krefft’s Pouched Mouse. Size medium. Fur close and soft. General color above sandy- brown, below paler. Ears short, rounded, and very broad. Tail short, a prominent crest of black hairs, becoming longer towards the tip, on the upper side of its terminal half. Mamme ? Dimensions.—Head and body about five inches; tail about three and a half inches. Habitat.—South Australia. Type.—In the Australian Museum, Sydney. References.—Thomas, B.M. Catal. p. 276; Krefft, P.Z.S, 1866, p. 435, pl. xxxvi, DASYURUS. 15 Note.—As the only specimen known is mounted it is impossible to give any description of the palms and soles and their pads. In the type specimen, according to Krefft, the fourth premolar is absent, but seeing that it is present in all other members of the subfamily (except P. thorbeckiana, in which it is a variable character), this is doubtless an individual variation or peculiarity. Genus V.—DASYURUS, #. Geoffroy (1796). Body spotted. Form stout or slender, graceful. Ears long and narrow. Tail long, evenly- and thickly-haired throughout. Feet plantigrade. Toes subequal, with sharp, curved claws ; hallux very small or wanting. Soles granulated, nearly or wholly naked. Pouch opening vertically downwards. Mamme six or eight. +, 1 2.3.4 i 1.0.3.0 1.2.3.4 3 19 Dentition.—I. 123 (Ot p 12. 1.0.3.0? M. i234 x 2=42., Habits.—Terrestrial and arboreal; carnivorous and _insecti- vorous. Note.—The “ Native Cats” of the Australian region take the place of the Mustelide of the pale- and ne-arctic regions, and are equally destructive to poultry &c. 1, DasyuRUS HALLUCATUS, Gould (1842). North-Australian Native Cat. Size small; form slender. Fur short and coarse. General color above yellowish-brown spotted with white; below pale gray or yellow. ars large, thinly clothed with fine yellow hairs. Hallux present. Sole-pads smooth, well-defined, and transversely striated. Tail long, rather short-haired, its base colored like the body, but unspotted, the remainder black. Mamme eight. Dimensions.—Head and body about eleven inches ; tail about eight inches. Habitat.—Tropical Australia. References.—Thomas, B. M. Catal. p. 269; Gould, Mamm. Austr. i. pl. ii. 2. DasyuRuUS GEOFFROYI, Gould (1840). Black-tailed Native Cat. Size medium; form slender, Fur thick and soft. General color above olive-gray tinged with rufous and spotted with white; below white. Lars large, their backs brown with white margins. Hallux present. Soles granulated, the pads marked by rounded unstriated prominences. Tail long and rather bushy, the basal half above and fourth below colored like the back, but unspotted, the remainder black. Mamme six. 16 DASYURUS. Dimensions.—Head and body about sixteen inches ; tail about twelve inches. Habitat.—All Australia except the extreme North, and the coastal districts of the South-East. References.—Thomas, B.M. Catal. p. 268, pl. xxiii. figs. 1 (ear), 2 (sole); Gould, Mamm. Austr. i. pl. li. 3. DASYURUS VIVERRINUS, Shaw, sp. (1800). Common Native Cat. 1G I. Lower jaw of Dasyurus viverrinus, showing typical polyprotodont den- tition (natural size). Size medium; form slender. Fur thick and soft. General color above and below either pale gray or black, spotted with white. Ears large. Hallua absent. Soles granulated, without distinct pads. Tail bushy, its proximal three-fourths like the back, but unspotted, its tip white. Mamme six. Dimensions.—Head and body about eighteen inches ; tail about twelve inches. Habitat.—Eastern watershed of New South Wales ; Victoria ; South Australia ; Tasmania. References.—Thomas, B. M. Catal. p. 265; Gould, Mamm. Austr. i. pl. 1. Note.—This species, in both varieties, but mostly in the light- colored form, is as much, if not more, terrestrial than arboreal, living in dead logs, under rocks, or in holes in the cliffs, in which latter place they feed on dead fish, and probably crustaceans, mollusks, &c., and are thus frequently caught in baited fish-traps left bare by the tide or hauled up during bad weather. Fossil remains of this species have been discovered in the Wellington Caves, New South Wales, the Pleistocene Deposits of Gowrie, Queensland, and in Tasmania. DASYURUS. 17 4. Dasyurus GRAcILIS, Ramsay (1888). Slender Native Cat. Size small; form light and graceful. Fur short, close, and somewhat harsh to the touch. General color above and below deep blackish-brown, spotted with white, the spots on the sides and on the basal third of the tail largest and sometimes confluent. Ears rather short, thinly haired proximally outside, the inside with a tuft of long hairs on the anterior margin. Hallux present. Claws long and powerful. Tail long, slender, the terminal inch tufted, colored like the body. Mamme? Dimensions..—Head and body thirteen inches; tail nine and a half inches. Habitat.—Bellenden-Ker Range, Northern Queensland. Type.—In the Australian Museum, Sydney. Reference.—Ramsay, P.L.S. N.S. Wales, (2) iii. p. 1296 (1888). Note.—Were it not for the indisputably adult dentition of the unique specimen on which Dr. Ramsay has founded his new species, and that evidence, presumably reliable, points to the existence in the same district of a Spotted-tailed Dasyure as large as or even larger than the southern D. maculatus, I should have been inclined to consider this specimen as merely an aborted tropical form of that species; until, however, further research has undeniably proved the presence there of two so widely separated races it is perhaps better to keep them apart. It is worth mentioning that both in its fauna and flora the Bellenden-Ker Ranges shew more distinct affinities to the Papuan than to the restricted Australian Subregion ; for instance the Rhododendron flourishes in a wild state in these mountains only of Australia, having evidently travelled round from the Himalayas along the highlands of New Guinea, and so down the northern Queensland Ranges; similarly such typical Papuan forms as Dendrolagus among Mammals, Casuarius among Birds, Papuina among Molluscs, Pericheta among Earthworms, with many others, have found their way into our fauna. 5. Dasyurus macuuatus, Kerr, sp. (1792). Spotted-tailed Native Cat. Size large ; form stout and heavy. Fur thick and close. General color above dark brown with a rufous or orange tinge, but never black, with large white spots ; below white or pale yellow. Ears rather short and very thinly haired. Hallux present. Claws large and powerful. Tail very long, brown or rufous brown, spotted like the body. Mamme six. Dimensions.—Head and body about twenty-five inches ; tail about nineteen inches. B 18 SARCOPHILUS. Habitat.—From Central Queensland to Victoria, principally on the Ranges but extending to the coast line ; Tasmania. References.—Thomas, B.M. Catal. p. 263, pl. xxiv. fig. 3 (raght molar®); Gould, Mamm. Austr. i. pl. xlix. Tt seems to me that there must have been some extraordinary misapprehension on the part of Mr. Thomas, or some misrepre- sentation on the part of his correspondents, when he penned the sentence (loc. cit. p. 265) asserting the ‘“ great rarity on the continent ”—i.e. the mainland of Australia—of this species in comparison with its ‘‘commoness in Tasmania ;” as a matter of fact D. maculatus is by no means uncommon—nor seemingly has it any present intention of dying out—in the mountainous and coastal districts of eastern Australia from northern Queensland, through New South Wales and Victoria to South, and possibly West Australia. It may be worth mentioning that the largest, stoutest, and heaviest example I have yet seen was caught, in company with five others, on Manly Beach, a suburb of Sydney. For these and other reasons I cannot in any wise agree with Mr. Thomas as to the approaching extermination of this species on the mainland, nor can I allow, though confessedly unable to promulgate a more ostensible theory, that the causes which conduced to the annihilation, at what must have been a very recent period, of Sarcophilus and Thylacinus from Eastern Australia, can have in any degree affected D. maculatus, the former having been purely, or at the least mainly terrestrial, while the latter is most emphati- cally an arboreal Mammal. If the Dingo, as suggested by Mr. Thomas, had anything whatever to do with the extermination of our Native Cats, the first to disappear would have been D. viver- rinus by far the most terrestrial of all the Dasyures. Genus VI.—SARCOPHILUS, /. Cuvier (1837). Body blotched with white. Form very stout and powerful. Muzzle short and broad. Ears broad and rounded. Tail moderate, evenly hairy. Feet plantigrade. Toes subequal, with well- developed curved claws; hallux absent. Soles naked, without defined pads. a0 1.2.3.4 1.0.3.0 1.2.3.4 16) Dentition.—I. 753-> CE eae, ee Habits.—Fossorial ; carnivorous. Note.—A fossil species, S. laniarius, Owen, sp., is found in the Wellington Caves and at Gowrie, Queensland. 1. SaRcoPpHILUS URSINUS, Harris, sp. (1808). Tasmanian Devil. Fur thick and close, consisting largely of soft woolly underfur. General color above and below black or blackish-brown, with a BB PERAMELID&. 19 variable number of white patches on the neck, shoulders, rump, and chest, the pectoral patch only being constant. Ears hairy, with well-marked basal tufts. Soles naked, coarsely granulated, and without pads ; a small transversely-striated pad at the extreme tip of each toe. Tail short, uniformly thickly hairy. Mamme ? Dimensions.—Head and body about twenty-eight inches ; tail about twelve inches. Habitat.—Tasmania. References.—Thomas, B.M. Catal. p. 259, pl. xxiv. fig. 2 (right molar*); Gould, Mamm. Austr. i. pl. i: Genus VII.—THYLACINUS, Vemminck (1827). Back transversely banded with black. Size large; form wolf-like. Muzzle long and slender. Ears of medium size. Tail well developed, short-haired. Feet markedly digitigrade. Toes sub- equal, with short, thick, conical claws. Hallux absent. Pouch opening backwards. Mamme four. Marsupial bones rudimentary. 12.3.4 q 1 1.0.3.4 i, oo Denistion.—I. 75, , C. 3, P. Tam M- gag x 2=46 Habits.—Terrestrial ; carnivorous. Note.—Thylacinus speleus, Owen, a fossil form of larger size than the living representative is also known from the Wellington Caves and the Queensland Pleistocene. 1. THYLACINUS CYNOCEPHALUS, Harris, sp. (1808). Tasmanian Wolf. Fur short, close, and crisp. General color above pale finely grizzled gray- ‘brown, with a faint yellowish or tawny tinge ; below slightly paler. Round the eyes, edges and base of the ears "nearly white. Posterior part of back with about sixteen blackish-brown transverse bands, descending on the rump nearly to the knee. Soles naked, coarsely granulated, without defined pads. Tail with indistinct crests above and below, its tip blackish. Dimensions.—Head and body about forty-four inches ; tail about twenty-one inches. Habitat.—Tasmania. References.—Thomas, B.M. Catal. p. 255, pl. xxiv. fig. 1 (right nolar®); Gould, Mamm. Austr. i. pls. lili. (head), liv. Family I1.—PERAMELIDA. Bandicoots. Hind limbs decidedly the longer. Fore feet with two or gener- ally three of the middle digits long, and clawed, the others rudi- 20 CHCROPUS mentary or absent. Hind feet syndactylous, with four or five toes very unequal in size ; hallux rudimentary or absent ; second and third toes slender, united ; fourth strongest, long, with a large claw ; fifth present, clawed. Clavicles absent. Ccecum present. Pouch present, opening backwards. Genus I.—CH@ROPUS, W. Ogzlby (1838). Form light and slender. Muzzle short and narrow. Ears long and narrow. Fore feet with the first and fifth digits absent, the fourth rudimentary, the second and third fully developed with long, slender claws. Hind feet with the hallux absent, the fifth toe rudimentary, and the fourth very large. Tail cylindrical, slightly crested along the upper surface. Mamme eight. oye 1.2.3.4.5 1 1.0.3.4 1.2.3.4 ej ae Dentition.—I. [Loom C. p es 03! M. 1.234 x 2=48. Habits.—Terrestrial ; fossorial ; omnivorous. 1. Cua@Ropus CASTANOTIS, Gray (1842). Pig-footed Bandicoot. Size small ; form delicate. Fur coarse and straight, but not spiny. Ears thinly haired, dull chestnut-brown behind, darkening towards the tip. General color above coarse grizzled gray with a tinge of fawn ; below white. Limbs long and slender. Tail short, black above, gray on the sides and below. Dimensions.—Head and body about ten inches ; tail about four inches. Habitat.—Western New South Wales and Victoria; South and West Australia ; (Northern Territory ‘). Type.—tIn the Australian Museum, Sydney. References.—Thomas, B. M. Catal. p. 250; Gould, Mamm. Austr. i. pl. vi. Genus II.—PERAMELES, Geoffroy (1803). Form varying from stout and clumsy to light and delicate. Muzzle long and pig-like. Ears variable in size. Fore feet with the first and fifth digits short and clawless, and the three middle digits long and subequal with curved fossorial claws. Hind feet with the hallux short and clawless, the second and third toes with flat twisted nails, the fourth long and powerful with a stout pointed claw, and the fifth similar but smaller. Tail tapering ; short- haired or nearly naked. Mamme six or eight. OA 1.2.3.4.5 or 0 1 1.0.3.4 1.2.3.4 6 ee Dentition.—I1 iar ee C. Dp 1B. 103” M, 1234 xX 4 = 46 or 48, Habits. —Terrestrial ; fossorial ; omnivorous. Note.—The Bandicoots do a great amount of damage to culti- vated lands and gardens, not only by digging up and consuming PERAMELES. ' 21 large quantities of the seeds, roots, and bulbs planted by the farmers, but also by being the especial enemy of earth-worms, which by their constant and equable trituration of the soil, and their introduction below the surface by means of their excreta of such foreign substances as decaying leaves, &c., are generally ac- cepted now as most potent friends of agriculture. These animals fall naturally into two very distinct groups, the former of which, represented by P. gunnz and its allies, inhabits the “stony ridges of the hotter and more exposed parts,” while the latter, repre- sented by P. obesula and its allies, is restricted to “low swampy grounds covered with dense vegetation.” From the Caves of the Wellington Valley, N.S. Wales, numer- ous remains of Bandicoots have been secured in a fossil state, but agreeing so intimately with recent forms as to make it injudicious to separate them; the species represented are as follows: Pera- meles bougainvillir, P. nasuta, P. obesula, an undescribed species of Perameles and Peragale lagotis. 1, PERAMELES BOUGAINVILLII, Quoy & Gaimard (1824). Western Striped Bandicoot. Size small; form light and delicate. Fur coarse, but not spinous. Muzzle long and slender. Ears long, narrow, and pointed, reach- ing when laid forward beyond the eye; their backs grayish-flesh- color, slightly darker on the anterior portion of their terminal half. General color above grizzled olive-gray ; below white ; sides of rump with ill-defined stripes. Soles hairy and black posteriorly ; naked, granulated, and flesh-colored anteriorly; con- spicuous round pads at bases of fourth and fifth toes. Tail moderate, brown above, white below. Mamme eight. Dimensions.—Head and body about nine inches; tail about four and a quarter inches. Habitat.—West Australia. References.—Thomas, B.M. Catal. p. 246, pl. xxi. figs. 7 (ear), 8 (sole) ; Gould, Mamm, Austr. i. pl. x. la. P. BOUGAINVILLI, var. FAscIATA, Gray (1841). Eastern Striped Bandicoot. Differs from the typical form only in the stronger contrast between the dark and light patches on the back of the ears, and in the rump-stripes being well defined and conspicuous. Habitat.—South-eastern and southern Australia. References.—Thomas, B. M. Catal. p. 248; Gould, Mamm. Austr. i. pl. viii. 22 PERAMELES. 2, PERAMELES GUNNI, Gray (1838). Tasmanian Striped Bandicoot. Size large; form slender. Fur soft, not spinous. Muzzle long and slender. Ears long and pointed, reaching when laid forward beyond the eye ; their backs yellowish-brown, with a darker blotch on the anterior portion of their terminal half. General color above grizzled yellowish-brown; below white or yellowish-white ; sides of rump with four vertical light bands. Soles hairy and black posteriorly, naked and white anteriorly ; small round striated pads at bases of fourth and fifth toes. Tail very short, slender, white except on a short basal portion of the upper surface. Mammee ? Dimensions.—Head and body about sixteen inches ; tail less than four inches. Habitat.—Tasmania, and probably the coastal region of South- eastern Victoria. References.—Thomas, B. M. Catal. p. 245; Gould, Mamm. Austr. 1. pl. ix. 3. PERAMELES NASUTA, Geoffroy (1804). Long-nosed Bandicoot. Size large; form slender. Fur coarse, hispid, and slightly spinous. Muzzle very long and slender. General color above dull olivaceous-brown ; below white. Ears long, narrow, and pointed. Inner side of limbs and feet white. Soles granulated, black and thinly hairy posteriorly, white and naked anteriorly. Tail of moderate length, brown above, paler below. Mamme ? Dimensions.—Head and body about sixteen inches ; tail abou five inches. Habitat.—Eastern Australia. References.—Thomas, B. M. Catal. p. 242, pl. xxii. figs. 5 & 6 (skull) ; Gould, Mamm. Austr. 1. pl. xi. 4, PERAMELES MACRURA, Gould (1842). North Australian Bandicoot. Size large; form rather stout. Fur short, coarse, and spiny. General color above coarsely grizzled yellow and black ; below white or yellowish-white. Ears short and broad, their backs brown, narrowly margined with white. Hands and feet brown, or mixed brown and white. Soles naked and coarsely wrinkled. Tail rather long, brown above, white below. Mamme eight. Dimensions.—Head and body about sixteen inches ; tail about seven inches. Habitat.— Northern Australia. References.—Thomas, B.M. Catal. p. 234. PERAGALE. 23 5, PERAMELES AURATA, Ramsay (1887). Golden Bandicoot. Size small; form rather stout. Fur coarse and spiny. General color above rich golden brown pencilled with black ; below white. Kars short and broad. Dimensions.—Head and body about eight and a half inches. Habitat.—North-western Australia. 7T'ype.—In the Macleay Museum, Sydney University. Reference.—Ramsay, P.L.S., N.S. Wales (2) ii. p. 551 (1887). 6. PERAMELES OBESULA, Shaw, sp. (1793). Short-nosed Bandicoot. Size medium ; form stout. In all other respects externally resembling the P. macrura, except that the tail is shorter, the feet rather less heavy, and the general color lighter. Dimensions.—Head and body about fourteen inches ; tail about five and a half inches. Habitat.—Australia south of the tropics ; Tasmania. References.—Thomas, B.M. Catal. p. 231, pl. xxi. fig. 5 (ear); Gould, Mamm. Austr. i. pl. xii. Genus IIJ.—PERAGALE, Gray (1841). Form light and delicate. Muzzle long and narrow. Ears very long. Fore feet with the first and fifth toes rudimentary and clawless, and the three middle toes long, with powerful curved claws. Hind limbs much longer than the fore. Hallux absent externally. Soles hairy. Tail long, conspicuously crested on the terminal half above. + 1.2.3.4.5 1 p 1.0.34 1234. « Denitition.—I. 555, C. 3, P- rosa M- toaa x 2 = 48. Habits.—Terrestrial ; fossorial ; omnivorous. 1. PERAGALE LEUCURA, Zhomas (1887). White-tailed Rabbit-Bandicoot, Size small ; form slender. Fur long, soft, and silky. General color above pale yellowish-fawn ; below white. ars thinly clothed with fine silvery hairs. Limbs white. Greater part of the soles hairy. Tail moderate, slender, tapering, short-haired except on the terminal third above, uniform white. Dimensions. —Of adult unknown. Habitat.—Unknown ; probably Central or North-Central Australia. References: —Thomas, B.M. Catal. p. 225, pls. ii., xxi. figs. 9 (palm), 10 (sole). 24 é PERAGALE. 2. PERAGALE LAGoTIS, Reid, sp. (1836). Common Rabbit-Bandicoot. Size large ; form light and delicate. Fur very long, soft, and silky. General color above fawn-gray ; below white. Cheeks and bases of ears white or pale fawn. Ears nearly naked, their edges and the anterior part of the backs thinly clothed with pale brown hairs. An indistinct darker vertical band on the sides of the rump. Outer sides of the fore and backs of the hind limbs dark gray grizzled with white ; remainder of limbs white. Soles almost entirely thickly hairy. Tail of moderate length, thickly hairy throughout, the basal third colored like the body, the middle third black or dark brown, the terminal third white and prominently crested above. Dimensions.—Head and body about eighteen inches; tail about nine inches. Habitat.—South and West Australia. References.—Thomas, B. M. Catal. p. 223, pl. xxii. fig. 1 (hull ); Gould, Mamm. Austr. i. pl. vii. Suborder II.—Diprotodontia. Normal characters.—Incisors three in the upper, one in the lower jaw, the latter long and powerful. Canines usually small, much smaller than the incisors, almost invariably absent below. Molars bluntly tuberculate or ridged. Frugivorous, graminivorous, phytophagous, herbivorous, rhizo- phagous ; rarely insectivorous and mellivorous. Exceptions.—One upper incisor only in each ramus in Phasco- lomys ;, second lower incisor present in Phalanger, Trichoswrus, Gymnobelideus, Dromicia, Distechurus, and Acrobates ; occa- sionally in Pseudochirus and Petauroides ; second and third in Dactylopsila ; second and occasionally third in Petawrus. Family I1I.—PHASCOLOMYID/i. Wombats. Form stout and clumsy. Muzzle short and broad. Limbs subequal, very thick and strong. Fore feet with five subequal digits, each with a stout claw. Hind feet with the hallux short and clawless ; the other toes with long, curved claws; the second and third witha slight tendency to syndactyly. Tail rudimentary. Stomach simple. Ccecum present. Pouch present. Mamme ? Genus ].—PHASCOLOMYS, JZ. Geoffroy (1803). Characters as those of the family. PHALANGERIDA. 25 eet 1.0.0 ~ 0 0.0.0.4 2 Saw at ay Dentition.—I. yy ©-m P: soow M- Toaa Xx 2= 24. Habits.—Fossorial ; rhizophagous. 1. PHASCOLOMYS MITCHELLI, Owen (1838). Common Australian Wombat. Size large. Rhinarium large, naked, and black. Fur coarse, harsh, and hispid. Color above and below either yellow, grizzled yellow and black, or black. Ears short, rounded, and well- haired. Ribs of the exceptional number of fifteen. Dimensions.—Head and body about forty-four inches. Habitat.—New South Wales, Victoria, and South Australia. References.—Thomas, B. M. Catal. p. 213; Gould, Mamm. Austr, 1. pls. lvl. (head), lviii. 2. PHAscoLoMys uURSINUS, Shaw, sp. (1800). Tasmanian Wombat. Differs in no respect from the preceding except in its smaller size. Color above and below uniform dark grizzled grayish-brown. Dimensions.—Head and body about thirty-eight inches. Habitat.—Tasmania, and Islands in Bass’ Straits. References.—Thomas, B. M. Catal. p. 215; Gould, Mamm. Austr. 1. pls. lv. (head), lvi. 3. PHASCOLOMYS LATIFRONS, Owen (1845) Hairy-nosed Wombat. Size moderate. Rhinarium hairy, velvety to the touch, and white. Fur straight, soft, and silky. General color above mottled gray ; tip of muzzle, a spot above and below the eyes, cheeks, throat, and chest white ; chin black ; rest of underside dirty gray. Ears comparatively long, narrow, and pointed; outwardly sparsely clothed with black hairs, inwardly naked. Ribs of the normal number of thirteen. Dimensions.—Head and body about forty inches. Habitat.—South Australia. References.—Thomas, B. M. Catal. p. 217; Gould, Mamm. Austr. i. pls. lix. (head), 1x. Family I[V.—PHALANGERID. All the feet with five digits, those of the fore limbs generally subequal ; those of the hind limbs syndactylous, fairly stout and well developed ; fourth toe the longest, the fifth but little smaller ; 26 PHASCOLARCTIN ©. hallux present, large, widely opposable, with a broad, nailless, terminal pad. Tail (except in Phascolarctus) very long, and almost always prehensile. Stomach simple. Ccecum present (except in 7arsipes). Pouch well developed, opening backwards. Subfamily I.—PuHascoLarctinm. Tail wanting. Muzzle short and broad. Tongue not extensile. Cheek-pouches present. Ccoecum large and complicated. Teeth large. Genus IL—PHASCOLARCTUS, Slainville (1816). Size large ; form very stout and clumsy. Fur thick and woolly. Ears large, thickly furred. Flanks without flying-membrane. Fore toes subequal, their lengths in the following relative order— 4, 3, 5, 2, 1; the first and second opposable to the others. Claws thick, strong, and sharply pointed. Palms and soles granulated without striated pads. Tail rudimentary. Mammez two. Ribs numbering eleven only. Dentition.—I. 725, C. & P. gopa M. (84 x 2=30. Habits.—Arboreal ; phytophagous. Note.—A fifth lower molar is occasionally developed. 1. PHASCOLARCTUS CINEREUS, Goldf., sp. (1819). Koala; Native Bear. Fig. 2. Side view of skull of Phascolarctus cinereus, reduced one half. General color above gray ; below white or yellowish-white. Rhinarium thinly clothed with minute hairs. Ears rounded, the hairs on their backs black tipped with white ; elsewhere white. ~ rump dirty yellowish-white, sometimes irregularly spotted. Hands and feet white. TRICHOSURUS. rafg Dimensions.—Head and body about thirty-two inches. Habitat.—Eastern Australia. References.—Thomas, B. M. Catal. p. 210; Gould, Mamm. Austr. i. pls. xiii. (head), xiv. Subfamily I[.—PHaLancERinas. Australian Opossums. : Tail well developed, generally prehensile. Muzzle short and broad. Tongue not extensile. No cheek-pouches. Cocum present, large. Stomach simple. Teeth large. Genus IL—PHALANGER, Storr (1780). Size large or medium; form stout. Fur thick and woolly. Ears medium or short. Flanks without flying-membrane. Fore toes subequal, their lengths in the following relative order— 4, 3, 5, 2, 1. Claws long, stout, and curved. Soles naked, striated ; pads large and ill-defined. Tail strong, its terminal portion naked all round, smooth or granulated, prehensile. Mamme four. Dentition.—I. +25, C. % P. foep M. ey—16+4 x 2=40. Habits.—Arboreal ; phytophagous. 1. PHALANGER MACULATUS, ZL. Geoffroy, sp. (1803). Spotted Cuscus. Size large. Fur soft. Top of muzzle above rhinarium thinly haired. Ears small, thinly clothed both inside and outside with soft woolly hair. General colors above various combinations of white, rufous, and black; below white tinged with yellow or rufous. Tail generally deep yellow, furry from one-half to three- fourths of its length above, and from one-third to one-half below. Dimensions.—Head and body about twenty-six inches ; tail about nineteen inches. Habitat.—Northern Australia (Cape York District); Southern New Guinea ; Austro-Malayan subregion from Saleyer eastward. References.—Thomas, B. M. Catal. p. 197, pl. xxi. fig. 2 (ear); Gould, Mamm. Austr. i. pl. xxi. (@ ). Genus III.—TRICHOSURUS, Lesson (1828). Size large ; form stout. Fur thick and woolly. Ears medium or short. Flanks without flying membrane. Fore toes subequal, their lengths in the following relative order—4, 3, 2, 5, 1. Claws large and strong. Soles thickly hairy under the heels ; the rest naked, with low rounded ill-defined pads. Tail strong, its 28 TRICHOSURUS. terminal third or half naked beneath ; its extreme tip naked all round. , P- , M.S = 30. Habits.—Insectivorous. Note.—The generic title Phyllorrhina used by Bonaparte in 1831 for these Bats is inadmissable, no description having been given (see Blanford, Proc. Zool. Soc. 1887, p. 635). 1. HipposipERUS CERVINUS, Gould, sp. (1853). Fawn-colored Horseshoe Bat. Ears much shorter than the head ; lower third of the outer margin of conch with a small, acutely pointed projection. Horse- shoe much narrowed in front of the nasal apertures with two external secondary leaflets. Frontal glandular sac large. Thumbs MEGADERMA., 85 and feet small. Wing-membrane extending to the tarsus. Inter- femoral membrane of moderate size, triangular. Extreme tip of tail free. Fur reddish-brown, darkest above. Dimensions.—Head and body about two inches; tail about one inch ; forearm about one and three-fourths inch. Habitat.—York Peninsula; Aru Islands; Waigiou; New Guinea ; Duke of York Islands. References.—Dobson, B.M. Catal. Chiropt. p. 142, pl. ix. fig. 7 (front view of head); Gould, Mamm. Austr. iii. pl. xxxiv. 2. HIPPOSIDERUS BICOLOR, Zemminck, sp. (1835-1841). var. a. H. aruensis, Gray (1858). Brown Horseshoe Bat. Ears moderate, about equal in length to the head, oval ; the upper third of the outer margin straight. Horseshoe small and square, scarcely as wide as the transverse terminal leaf, the concave front surface of which is divided into four cells by three distinct vertical ridges ; no secondary leaflets ; frontal glandular sac well developed in males, rudimentary in females. Wing-membrane extending to the ankle or tarsus. Interfemoral membrane slightly angular behind. Extreme tip of tail free. Fur above very dark brown, almost black ; below grayish-brown. Dimensions.—Head and body about one and three fourths inch; tail rather less than an inch; forearm about one and a half inch. Habitat.— Albany Island, Cape York ; Aru Islands. Reference.—Dobson, B.M. Catal. Chiropt. p. 150. Family IZI.—NYCTERIDAs. Nasal apertures situated upon the upper surface of the muzzle, and margined by distinct cutaneous appendages. Ears large, united, with well developed tragi. Index finger with or without a short phalanx. Premaxillary bones cartilaginous or small. Upper incisors absent or very small; when present close together. Subfamily I.—MraaprermMina. Nostrils at the bottom of a concavity near the extremity of the muzzle, concealed by the base of a large cutaneous process ; tail very short, in the base of the large interfemoral membrane ; pre- maxillaries cartilaginous. Genus I.—MEGADERMA, Geoffroy (1810). Muzzle cylindrical, elongated. Nostrils in a slight depression near the extremity of the muzzle, surrounded by a naked cutane- 86 MEGADERMA. ous expansion, which forms a vertical process posteriorly. Lower lip projecting slightly beyond the upper. Ears large, partially connected ; tragus long, bifid. Index finger with a short bony phalanx. Toes subequal; the outer with two, the others with three phalanges. Calcaneum distinct. Tail very short, only discernible in skeletons. Interfemoral membrane large, concave behind. Dentition.—I. > Cp Pp >, (Australian and Oriental Regions) or i-5 (Ethiopian Region), M. $=) =28 or 26. Habits.—Carnivorous and insectivorous. Some, probably all, of the members of this genus are sanguinivorous and carnivorous, feeding not only on insects but also on smaller kinds of Bats and other small Mammals, and even Frogs and Fishes, while it may be presumed that small Birds and Reptiles would prove equally acceptable. This habit has been specially noticed by several observers in the Indian J. lyra. 1. MecapErMA GiIGcAs, Dobson (1880). Great Blood-sucking Bat. Lower jaw projecting beyond the upper. Ears considerably longer than the head, conjoined for nearly half the length of the inner margin, oval and rounded off above. Tragus large, bifid, the posterior lobe long, narrow, and acutely pointed, the anterior lobe scarcely half the length of the posterior, broad at the base, convex in front, and obtusely rounded above. Nose-leaf with convex sides, the anterior concave disc large, the external margin thickened and adherent to the muzzle beneath; base of the longi- tudinal process cordate. Extremity of the second finger extending beyond the middle of the first phalanx of the third finger. Wing- membrane from the back of the foot. Tail rudimentary. Inter- femoral membrane large. A well marked postorbital process not perforated by a foramen. Terminal third of the fur above pale grayish-brown, beneath almost white, as also are the ears, nose- leaf, and membranes. Dimensions.—Head and body about five and a third inches ; forearm about four and a fifth inches. Habitat.—Wilson’s River, Central Queensland. Reference.—Dobson, Proc. Zool. Soc. 1880, p. 461, pl. xlvi. figs. @ (animal), b (upper view of skull). Family IV.—VESPERTILIONIDA. Nasal apertures simple, crescentic or circular, situated at th® extremity of the muzzle, without cutaneous appendages. Ears large or medium, generally separate, with rather large tragi. Tail NYCTOPHILUS. 87 long, produced to the hinder margin of the large interfemoral membrane. Upper incisors distant from one another. Genus L—NYCTOPHILUS, Leach (1822). Muzzle narrow, thinly covered with short hairs; glandular prominences well developed. Crown of the head slightly elevated above the face line. Nostrils with their upper margins continu- ous with the base of a small cordate nose-leaf. Ears large, oval, and connected ; tragus short and triangular. Eyes large. Wings from the bases of the toes. ‘Tail slightly projecting beyond the interfemoral membrane. Upper incisors unicuspidate, close to the canines. Dentition.—I. 2, C. 5, P. > M. 3 =30. Habits.—Insectivorous. Note.—This genus takes the place in the Australian Region of the Pale- and Ne-arctic Plecotus. 1. NycToPHILUS TIMORIENSIS, Geoffroy, sp. (1806). Australian Long-eared Bat. Ears longer than the head, connected on the forehead by a well developed band ; the tip rounded ; upper third of outer margin of conch straight. Tragus short, triangular, and subacute. Glandular elevation behind the short nose-leaf longitudinally grooved in the middle. Broad extremity of nose-leaf upwards and free. Extreme tip of tail free. Fur above varying from dark to light brown; below from pale brown to white. Dimensions.—Head and body about two inches ; tail and fore- arm about one and four-fifths inch each. Habitat.—All Australia, Tasmania, and the neighboring Islands ; from Timor to the Fiji Islands. References.—Dobson, B.M. Catal. Chiropt. p. 172, pl. xi. fig. 7 (front view of head); Gould, Mamm. Austr. iii. pls. xxxvi., (. geoffroyt); xxxvil. (N. gouldi); xxxviii. (MN. unicolor); xxxix. (NV. timoriensis). Note.—Owing to the great variation in size, coloration, and the development of the glandular prominences Tomes divided J. timoriensis into four distinct forms under the specific names geoffroyt, tumoriensis, gouldi, and wnicolor; these however can at the most be only regarded as races of Geoffroy’s original species, 2. NYcTOPHILUS WALKERI, Thomas (1892). Walker’s Bat. Ears when laid forwards not quite reaching to the nose-leaf, connected by a band across the forehead ; the small lobe on the 88 VESPERUGO. inner surface of the base of the outer margin short and well defined. Fur shorter and paler in color than in the preceding species, especially on the under surface, where the hairs are tipped with dirty white. Dimensions.—Head and body of type specimen ( ? ) rather less than two inches; tail one and a half inch ; forearm one and one- third inch. Habitat.—Northern Territory (Adelaide River). Reference.—Thomas, Ann. Nat. Hist. (6) ix. p. 405. Note.—The almost entire absence of a transfrontal band, along with the larger size, longer and broader ears with a more convex inner margin, separate the WV. microtis, Thms. (Ann. Nat. Hist. (6) ii, p. 226) of South-eastern New Guinea from this species. Genus II.— VESPERUGO, Keyserling & Blasius (1839). Form comparatively stout. Muzzle very broad and obtuse ; glandular prominences well developed. Crown of head flat or very little elevated above the face line. Nostrils sublateral, simple, crescentic. Ears short, broad, and triangular, obtusely pointed, separate ; tragus generally short and obtuse. Calcaneum witha small postcalcaneal lobe on its posterior margin. Feet short and broad. Upper incisors in pairs separated by a wide interval. a 4 q 1-1 p 2-2, 1-1 3-3 ‘ Dentition. —I. 3, C. =, P. 5 or a=, M. Sy = 34 or 32. Habits.—Insectivorous. 1. VESPERUGO PUMILUS, Gray, sp. (1841). Little Bat. Muzzle not very obtuse. A shallow furrow between the muzzle and the glandular prominences. Ear-conches short and funnel- shaped ; middle third of outer margin and lower two-thirds of inner margin very convex; the tips short and rather abruptly rounded off. Tragus well developed and rather broad. Wings extending to the bases of the toes. Postcalcaneal lobe long and convex behind. Tip of tail free. Fur above and below black, the extreme tips above ashy or grayish, the terminal fifth below white or pale ash-color. Dimensions.—Head and body about one and a half inch ; tail about one anda third inch; forearm about one and a fourth inch. Habitat.—All Australia and Tasmania, References.—Dobson, B.M. Catal. Chiropt. p. 201, pl. xii. fig. 2 (ear); Gould, Mamm. Austr. iii. pl. xlvi. CHALINOLOBUS. 89 2. VESPERUGO ABRAMUS, Z'emminck, sp. (1835 - 1841). Yellow-headed Bat. Muzzle obtuse. Glandular prominences on the sides large and rounded, causing a furrow between them and the crown of the head. ar-conches broadly triangular, rounded at the tips; the outer margin almost straight. Tragus moderate. Wing-membrane attached to the bases of the toes. Postcalcaneal lobe distinct and rounded. Tip of tail free. Head and face between the eyes densely covered with moderately long fur ; space in front of the ears, about the eyes, and extremity of muzzle generally almost naked. Fur above dark brown, tipped with light yellowish-brown; head and neck wholly yellowish-brown ; below sooty-brown, the tips lighter than those of the upper surface. Dimensions.—Head and body about one and four-fifths inch ; tail about one and a half inch; forearm about one and a third inch. Habitat.—North Australia ; the Oriental Region from Ceylon to Southern Japan, and the Malay Archipelago ; and in summer entending westwards to Middle Europe. Reference.—Dobson, B.M. Catal. Chiropt. p. 226. 3. VESPERUGO KREFFTI, Peters (1869). Krefft’s Bat. Ear-conches shorter than the head, triangular, the tips rounded and, owing to a deep and abrupt emargination on the upper third of the outer margin, distinct, Tragus acutely pointed and curved inwards, with a distinct, acutely triangular lobe at the bases of the outer margin. Wing-membrane attached to the bases of the toes or to the metatarsus. Postcalcaneal lobe very shallow. Cartila- ginous extremity of tail only free. Face in front- of the ears nearly naked, the glandular prominences with a few long hairs. Fur above dark reddish-brown ; below paler. Dimensions.—Head and body about two and two-fifths inches ; tail about two inches ; forearm rather shorter than the tail. Habitat.—New South Wales ; Tasmania. feferences.—Dobson, B.M. Catal. Chiropt. p. 232; Gould, Mamm. Austr. iii. pl. xlviii. Genus ITI.—CHALINOLOBUS, Peters (1866). Muzzle broad, generally very short and obtuse: glandular prominences well developed. Crown of head slightly raised above face-line. Nostrils sublateral, forming a prominent flattened central ridge on the upper surface of the muzzle, separated from the glandular prominences by a distinct groove. Ears short, broad, rhomboidal or ovoid; the tragus expanded above and 90 CHALINOLOBUS. curved inwards. Lower lip with a distinct fleshy lobule on either side near the angle of the mouth, projecting horizontally outwards. Wings from the bases of the toes. Upper incisors unequal and unicuspid ; the poe ones shots bibs inner long. Dentition. ae my op —— P, 2 —* (Australian) or iS * (African), M. $=} = 34 or 32, Habits.—Insectivorous, 1. CHALINOLOBUS MORIO, Gray, sp. (1841). Chocolate or Small-toothed Bat. Ears small, rounded off above. Tragus narrow at the base, expanded in the middle. Nostrils opening slightly downwards, the margins of the apertures sharply cut and projecting above, separated by a rather wide concave space having a small median ridge. Postcalcaneal lobe well developed, supported internally by a cartilaginous prop, the curved extremity of which forms its posterior margin. Tail wholly contained within the interfemoral membraue. Fur above dark brown, almost black, on the head and anterior half of the body, passing into dark chestnut-brown posteriorly ; below similar but slightly paler. Body fur rather long and thick. Base of interfemoral membrane between the thighs only furry. Dimensions.—Head and body about one and four-fifths inch; tail about one and seven-tenths inch; forearm about one and a half inch. Habitat—From southern Queensland through New South Wales and Victoria to South Australia; Tasmania; New Zealand. References.— Dobson, B.M. Catal. Chiropt. p. 248, pl. xiv. figs. 1 (ear), la (muzzle); Gould, Mamm. Austr. iii. pl. xli. (S. morio), xlii. (S. microdon); Thomas, Ann. Nat. Hist. (6) iv. p. 462. 2. CHALINOLOBUS SIGNIFER, Dobson (1876). Dobson’s Bat. Ears and nostrils as in C. tuberculatus. An erect transverse process on the face between and slightly in front of the eyes ; its free upper margin regularly convex. All other characters similar to those of the preceding species. Dimensions.—Head and body about two inches; tail about one and three-fourths inch; forearm about one and two-fifths inch. Habitat.—South Central Queensland. Reference.—Dobson, B. M. Catal. Chiropt. p. 250, pl. xiv. figs. 2 (front view of head), 2a (muzzle). Note.—Probably not distinct from the preceding species. SCOTOPHILUS. 91 3. CHALINOLOBUS GOULDI, Gray, sp. (1841). Gould’s Bat. Ears rather angular on the upper half, the tips rounded. Tragus broad above, the tip subtruncate. Nostrils prominent above, separated on each side by a small sulcus from the well developed glandular prominences. Lower lip with a distinct fleshy lobe. Postcalcaneal lobe well developed and rounded. Extreme tip of the tail projecting. Fur above on the head, neck, and shoulders black with a very faint reddish tinge ; the back yellowish-brown; below, the breast reddish or ashy, the abdomen, sides, wing- and interfemoral membranes pale yellowish-white. Dimensions.—Head and body about two and a half inches ; tail about two and a quarter inches; forearm about one and four-fifths inch. Habitat.—Eastern and South-eastern Australia, and Tasmania. References.—Dobson, B.M. Catal. Chiropt. p. 250, pl. xiv. figs. 4 (side view of head), 4a (interfemoral membrane), 4b (upper incisors); Gould, Mamm. Austr. iii. pl. xl. 4. CHALINOLOBUS NIGROGRISEUS, Gould, sp. (1863). Pied or Blackish-gray Bat. Ears very rhomboidal; the tip rounded. Tragus expanded outwards above. Nostrils prominent on the upper surface of the muzzle, projecting slightly by their inner margins in front, and closer together than those of any other species of the genus. Post- calcaneal lobe well developed and rounded. Last rudimentary joint of the tail free. Fur above deep black with gray or pale brown tips to the hairs ; below similar but with ashy tips. Dimensions.—Head and body about one and three-fourths inch ; tail and forearm each one and one-third inch. Habitat.—Northern and Eastern Australia. References.—Dobson, B.M. Catal. Chiropt. p. 251, pl. xiv. figs. 3 (ear), 3a (muzzle); Gould, Mamm., Austr. iii. pls. xliii. (Scotophilus picatus), xliv. (S. nigrogriseus). Genus IV.—SCOTOPHILUS, Leach (1822). Form stout. Muzzle short, obtusely conical, naked; glandular prominences variable. Crown of the head but little elevated above the face line. Nostrils close together, simple, lunate, open- ing to the front or sublaterally, their inner margins projecting. Ears short, longer than broad, with rounded tips. Tragus taper- ing, subacutely pointed, and curved inwards. Terminal rudi- mentary vertebra of tail protruding beyond the interfemoral membrane. Calcaneum weak. Wings attached to, or close to 92 SCOTOPHILUS. bases of toes. Upper incisors long, unicuspidate, acute, basally close to'the canines. a: 2qlt p ll 3—3 Dentition.—I. 4, ©. >, P. 5, M. = = 30. Habits.—Insectivorous. 1. ScoroPHILUS RUEPPELLI, Peters, sp. (1866). Ruppell’s Bat. Ears short, the tips obtusely rounded. Tragus rather narrow, subacutely pointed, the basal half of the outer margin with two distinct emarginations, the upper half slightly convex and sloping inwards ; no transverse ridge on its outer surface. Fur short, on the upper surface almost wholly confined to the body; dark brown above and below, the extreme tips above and the terminal fourth below ashy ; sometimes with a chesnut tinge throughout. Dimensions.—Head and body about two and three-fourths inches; tail not quite two inches ; forearm two inches. Habitat.—New South Wales. Reference.—Dobson, B.M. Catal. Chiropt. p. 263, pl. xv. fig. 2 (side view of head). 2. ScoroPpHILus GREYI, (Gray) Dobson (1875). Grey’s Bat. Ears short, triangular, the tips rounded. Tragus broad, obtuse, the basal half of the outer margin straight, the terminal half convex and sloping inwards; no transverse ridge on its outer surface. Postcalcaneal lobe small, but distinct, rounded. Fur short, the face in front of the eyes nearly naked ; chestnut-brown above and below, the extreme tips of the latter ashy. Dimensions.—Head and body about one and three-fourths inch; tail and forearm about one and one-fifth inch. Habitat.—Port Essington ; Liverpool Ranges, References.—Dobson, B.M. Catal. Chiropt. p. 263, pl. xv. fig. 4 (ear); Gould, Mamm. Austr. iii. pl. xlv. Genus V.—VESPERTILIO, Keyserling & Blasius (1839). Muzzle long, thickly hairy; glandular prominences small. Crown of head vaulted, slightly elevated above face-line. Nostrils sub- lateral, simple, crescentic. Lars oval, longer than broad, separate; tragus long, generally acute and attenuated upwards. Postcal- caneal lobe absent or very small. Upper incisors nearly equal, in pairs close to the canines. oa 4 1—1 3—3 3—3 Dentition.—I. ? C. Tp P. 39) M. 3—3 — 38. Habits.—Insectivorous. KERIVOULA. 93 1. VESPERTILIO ADVERSUS, Horsfield (1824). Great-footed Bat. Extremity of ear broadly triangular, with the angle rounded off; upper half of outer margin straight. Tragus well developed, the extremity straight. Wings from the ankles and the sides of the body. Interfemoral membrane forming a very acute angle behind. Feet very large. Tail projecting beyond the membrane to some extent. Calcaneum very long, extending at least three- fourths of the distance between the ankle and the tail. Fur of moderate length. Second upper premolar extremely small, placed quite inside, in the angle between the first and third premolars, not visible from without. Dimensions.—Head and body about two inches; tail about one and three-quarters inch ; forearm about one and a half inch ; foot about half an inch. Habitat.—From Siam through Java, Borneo and the Celebes to the northern half of Australia. References.—Dobson, B.M. Catal. Chiropt. p. 292, pl. xviii. fig. 4 (ear enlarged); Gould, Mamm. Austr, iii. pl. xlvii. 2. VESPERTILIO AUSTRALIS, Dobson (1878). Small-footed Bat. Extremity of ear broad and very obtusely rounded ; upper third of outer margin deeply concave. Tragus well developed, the narrow extremity rounded and slightly curved outwards. Wings from the bases of the toes. Interfemoral membrane forming an obtuse angle behind. Feet of moderate size. Only the extreme tip of the tail projecting. Calcaneum extending about half-way between the ankle and the tail. Fur short. Second upper pre- molar small, but in the normal position and so visible from without. Brown, the extreme tips above and the terminal third below lighter. Dimensions.—Head and body about one and four-fifths inch ; tail and forearm about one and one half inch; foot about one-third of an inch. Habitat.—New South Wales. Reference.—Dobson, B.M. Catal. Chiropt. p. 317. Genus VI.—KERIVOULA, Gray, (1842). Muzzle narrow and elongated ; glandular prominences very small and indistinct. Crown of the head considerably vaulted. Nostrils simple, circular, sublateral. ars funnel-shaped, dia- phanous, studded with glandular papille; tragus long, narrow, and acutely pointed. Wings from the bases of the toes. Calcaneum 94 KERIVOULA. long and strong, curved backwards, without postcalcaneal lobe. Outer incisor shorter than the inner one, sometimes minute. Dentition.—I. 5, C.7—3, P. 33, M. 3 =38. ibe. namangeanal ; forest-haunting. 1. KERIVOULA PAPUENSIS, Dobson (1878). Eastern Forest Bat. Ears extending nearly to the end of the muzzle when laid for- wards, the tips rounded, the outer margin with a deep concavity occupying its upper fourth. Tragus with a distinct rounded lobe at the base of its outer margin, succeeded by a deep notch. Fur above dark brown, with the terminal fourth shining yellow ; below paler brown, with the extreme tips shining gray ; forearm clothed with short adpressed golden hairs. Dimensions.—Head and body about one and four-fifths inch ; tail about the same length ; forearm about one and a half inch. Habitat.—North-eastern Australia; South-eastern New Guinea. Reference.—Dobson, B.M. Catal. Chiropt. p. 339. Genus VII.—MINIOPTERUS, Bonaparte (1837). Muzzle rather short and broad; glandular prominences well developed. Crown of the head abruptly and considerably elevated above the face-line. Nostrils simple, lunate, sublateral. Ears rhomboidal, separate ; tragus short and obtuse. First phalanx of middle finger very short. Wings to the ankles or the tibiz, attached to the inferior surface. Feet long and slender; toes subequal. Upper incisors short, weak, separated from the canines. Dentition.—l. > CLS a Lan 2 » M. 2 = 36. RO Le ie 1. MINIOPTERUS SCHREIBERSI, Vatterer (1819). Schreibers’ Bat. A deep horizontal groove beneath the eye. Ears much shorter than the head, very much rounded above, the outer margin straight above. Tragus rather more than twice as long as broad, rounded above. Wings to the ankles or to the extremity of the tibia. Feet long and slender. Tail wholly contained within the inter- femoral membrane, which is nearly naked above. Fur above and below grayish, sometimes reddish, the basal half of the hairs dark grayish-brown. Dimensions.—Head and body about two and one-fifth inches ; tail about the same ; forearm about one and three-fourths inch. TAPHOZOUS. 95 Habitat.—Australia and the Islands of Torres Straits; from New Guinea and the Malay Archipelago westward through the wholeof southern Asia and Europe; Africa from the Mediterranean to the Cape of Good Hope. Reference.—Dobson, B.M. Catal. Chiropt. p. 348. 2. MINIOPTERUS AUSTRALIS, Zomes (1858). Differs chiefly from MW. schreibersi in its smaller size and the distribution of the fur. Interfemoral membrane clothed as far back as a line drawn from one ankle to the other ; tibise covered with fine hairs. Fur dark reddish-brown throughout above; below darker brown basally, the extremities grayish. Dimensions.—Head and body about one and three-fourths inch; tail about the same ; forearm about one and three-fifths inch. Habitat.—Australia ; Loyalty Islands. Reference.—Dobson, B.M. Catal. Chiropt. p. 351. Family V.EMBALLONURIDA. Nasal apertures simple or valvular, situated at the extremity of the muzzle, without distinct cutaneous appendages. Ears large, often united, with short tragi. Tail partially free, either perfor- ating the interfemoral membrane and appearing upon its upper surface, or produced far beyond its posterior margin. Upper incisors separated in front. Subfamily I.— EmpBaLionurinm. Tail slender, perforating the interfemoral membrane and appear- ing upon its upper surface, or terminating in it. Legs Inog; fibule very slender. Upper incisors weak. Genus I.—TAPHOZOUS, Geoffroy (1812). Muzzle very conical, broad behind, very narrow in front, ter- minated by the slightly projecting inner margin of the valvular nostrils. Ears separate; tragus short, narrow in the middle, expanded above. Lower lip as long or slightly longer than the upper. Generally a glandular sac, opening anteriorly, between the angles of the lower jaw, more or only developed in the males. Tail perforating the interfemoral membrane, and appearing on its upper surface, capable of being partially withdrawn. Upper incisors often absent in adults. Dentition.—I. 7, O. =, P. 53, M. 3 = 30. Habits.—Insectivorous. 96 TAPHOZOUS. 1. TAPHOZOUS AUSTRALIS, Gould (1853). Sharp-nosed Bat. Lower lip scarcely grooved. Gular sac distinct but rather small in the males, absent in the females. Ears large, as long as or longer than the head. Radio-metacarpal pouch well developed. Wings from the ankles or tarsus. Tail slender. Interfemoral membrane clothed with fur as far as the point perforated by it. Fur rather long and dense, basally pure white above and below, the remaining three-fourths above dark brown, below paler. Dimensions.—Head and body about three inches ; tail about one and a third inch ; forearm about two and three-fourths inches. Habitat.—Australia and New Guinea. References.—Dobson, B. M. Catal. Chiropt. p. 382; Gould, Mamm. Austr. ili. pl. xxxii. 2. TAPHOZOUS FLAVIVENTRIS, (Gould) Peters (1866). Yellow-bellied Bat. Differs only from 7’. australis, in its color and superior size. Fur above uniform dark brown, below pale ochraceous yellow, whitish basally. Habitat.— New South Wales. Reference.—Dobson, B.M. Catal. Chiropt. p. 382. Note.—Dr. Ramsay’s 7’. hargravii, of which the type is in the Australian Museum, Sydney, is founded on a dried skin in very bad condition, and is possibly identical with this species ; in any case until good specimens in the flesh are obtained and an extended examination and comparison thus rendered possible, it is premature to give it a place in our fauna. The specimen was obtained in the Wollongong District, N.S. Wales. It is but right to state that Dr. Ramsay still considers the species to be good ; for the reason given above | can venture on no opinion. 3. TApHozous AFFINIS, Dobson (1875). Var. a. 7’. insignis, Leche (1884). Leche’s Bat. Lower lip deeply grooved. Gular sac large in the males, rudimentary in the the females; behind its aperture a small duplication of the integument provided with thickened edges. Kars shorter than the head. Upper margin of tragus jagged. Radio-metacarpal pouch absent. Wings from the ankles. Inter- femoral membrane naked. Fur above black with white bases, below pure silky white. Antebrachial and interfemoral membranes and the portion of the wing-membrane between the forearm and NYCTONOMUS. 97 the third finger white, between the first and third fingers black mottled with white along the latter. Dimensions.—Head and body about three inches ; tail about one inch ; forearm nearly three inches. Habitat.—South Australia. Reference.—Leche, Proc. Zool. Soc. 1884, p. 51, fig. 4 a. (side view of head showing lobature of left tragus); B. (right tragus,; c. (under view of head showing subsidiary sac ). Note.—In enumerating the points of difference between the typical 7. affinis of Dobson and his variety insignis, Prof. W. Leche lays stress on the color of the wing-membrane between the forearm and the third finger, but his description is word for word that of Dr. Dobson, so that, unless some clerical error has been committed, this difference (?) must be excised. In regard to the tragus it is noticeable that the form of the lobature in the, pre- sumably typical, example figured is totally different on either side, as indeed is noticed by its describer, leading us to surmise that this may be the result of accident, or else an individual peculiarity ; if this should prove to be the case there is nothing by which to separate this form from the typical species, except a rudimentary subsidiary gular sac in the male, hardly a sufficient difference on which to form even a variety. Prof. Leche can in any case be congratulated on having added a very distinct species of Taphozous to the Australian Fauna. Subfamily II.—Motossinam. Tail thick, produced far beyond the posterior margin of the interfemoral membrane, which is movable upon it. Legs short and strong with well developed fibule. Feet large ; the first toe and often the fifth, much larger than the others. Upper incisors strong. Genus II.—NYCTONOMUS, Geoffroy (1812). Extremity of muzzle broad, very obliquely truncated, projecting considerably beyond the lower lip, and terminated by the sharply cut margin of the nostrils. Ears united on the muzzle, or close together by the bases of their inner margins ; tragus short, never linear. Upper lip expansible, generally deeply grooved by vertical wrinkles. First and fifth toes much thicker than the others; backs of all the toes with long curved hairs. Upper incisors close to the canines at their bases, separate in front, their cusps converg- ing inwards and forwards. pee abel i! 2—2 Dentition.—lI. | or 7, C. Page Oho 3 ¢ =p a> 30 or 32. Habits.—Insectivorous, G 98 NYCTONOMUS. 1. Nycronomus pLicatus, Buchanan-Hamilton, sp. (1800). Plicated Bat. Ears united by a low band in front, evenly and broadly rounded off above. Tragus very small and quadrate, the upper margin slightly concave. Upper lip very thick, deeply grooved by vertical wrinkles. No gular sac. Wing-membrane from the lower end of the tibia. Fur very soft and dense ; above bluish- or smoky- black, below paler. Dimensions.—Head and body about two and three-fourths inches; tail about one and three-fourths inch ; forearm nearly two inches. Habitat.—South Australia; Tasmania; Malay Peninsula; Java; Sumatra; Borneo; Philippine Islands; India. References.-—Dobson, B.M. Catal. Chiropt p. 425 ; Leche, Proc. Zool. Soc. 1884, p. 51. 2. NYcTONOMUS AUSTRALIS, Gray, sp. (1838). White-striped Bat. Ears large, their inner margins not united, but rising close together from distinct points of origin. Integument of the ear- conch rather thin. Tragus short and broad, the outer margin distinctly concave mesially. Upper lip with short vertical wrinkles. A large gular sac with outwardly projecting hairs in the male, and but little developed in the female. Wing-membrane from the distal third of the tibia. Fur moderately long and dense ; above dark reddish-brown, below paler ; in the male the fur cover- ing the wing-membrane beneath the humerus and femur, from the sides of the body outwards is pure white; in the female white largely mixed with brown. Dimensions. —Head and body about three inches; tail about one and three-fourths inch ; forearm about two and a third inches. Habitat.—Australia ; New Guinea. References.—Dobson, B.M. Catal. Chiropt. p. 433, pl. xxii. fig. 9 (head); Gould, Mamm. Austr. iii. pl. xxxi. 3. Nycronomus ALBipus, Leche, (1884). Leche’s White-striped Bat. Differs from WV. australis in the following particulars: Lars much longer than the head, and united by a low band. Integu- ment of ear-conch thick and opaque. The gular sac and the white band of fur along the inner margin of the wing beneath fully developed in the female. Ge RODENTIA. 99 Dimensions.—Head and body about three and a half inches ; tail about two inches ; forearm about two and two-fifths inches. Habitat.—South Australia. Reference.—Leche, Proc. Zool. Soc. 1884, p. 50, fig. 3. a. (front and lower view of head); B. (side view of upper jaw); C. (side view of lower jaw). 4. NYCTONOMUS NORFOLCENSIS, Gray, sp. (1839). Norfolk Island Bat. Ears triangular, shorter than the head, separate, the outer margin of the conch straight, the tip broadly rounded. Tragus triangular, rounded above. Muzzle flat and obtuse. Upper lip with shallow vertical wrinkles. Nostrils opening sublaterally. Gular sac small in the male, rudimentary in the female. Wing- membrane from the ankle. Fur reddish-brown above, paler beneath. Lower incisors six. Dimensions.—Head and body rather more than two inches ; tail about one and a fourth inch; forearm about one and a half inch. Habitat.—Eastern Australia ; Norfolk Island. Reference.—Dobson, B.M. Catal. Chiropt. p. 439 ; 5. Nycronomus pErTersi, Leche (1884). Peters’ Bat. Differs from WV. norfolcensis in the following particulars only. Nostrils opening forwards. Gular’ sac absent in both sexes. Wing-membrane arising from the tibia a short distance behind the ankle. Dimensions.—Head and body about two and two-fifths inches ; tail and forearm about one and a third inch. Habitat.—South Australia. Reference.—Leche, Proc. Zool. Soc. 1884, p. 49, fig. 1. A. (side view of upper jaw); B. (front view of lower jaw). Order IV.—RODENTIA. Terrestrial, rarely arboreal or natatorial, diphyodont, placental mammals of small size ; with plantigrade or semiplantigrade, generally pentadactyle, unguiculate, rarely subungulate feet ; with clavicles (sometimes imperfect or rudimentary) ; with never more than two incisors in the mandible, and without canines ; premolars and molars rooted or rootless ; with tuberculated or laminated crowns, and arranged in an unbroken series, 100 MURIDA. To the Ropentra belong the greater number of living Mammals, and their distribution is practically cosmopolitan, but, as with the remaining Orders of EurneEria, they are not well represented in Australia, only one of the eighteen recognised Families being indigenous. The absence of canines and the large chisel-shaped incisors distinguish them from all other Mammals. The dental formula is, asa rule, very constant, and may be cited typically as I. +, C. $, PM. + or 3, M. 2. There are usually five digits in the hand, the pollex, however, being sometimes rudimentary or even absent. Family I1—MURID. Rodents of various habit, but generally terrestrial ; with con- tracted frontals ; with the lower root of the maxillary zygomatic process more or less flattened into a perpendicular plate. Malar short and slender, generally reduced to a splint between the maxillary and squamosal processes. Typically with a high per- pendicular infraorbital foramen, wide above and narrow below. Lower incisors compressed ; molars rooted or rootless, tuberculate or with angular enamel folds; premolars none, except in Sminthus,; pollex rudimentary ; tail generaly subnaked and scaly. The Rats constitute more than a third of the known Rodents, and are represented by thirty-five genera with a cosmopolitan distribution. The presence or absence of roots to the molars divide these into two distinct sections. Subfamily I.—Hypromyinz. Molars 2, divided into transverse lobes ; infraorbital opening variable ; incisive foramina very small. Genus I.—HYDROMYS, Geoffroy (1805). Molars two only in each ramus, divided into transverse lobes. Infraorbital opening crescentic, scarcely narrowed above, its external wall without an anteriorly projecting plate. Incisive foramina very small. Toes partially webbed. Distribution.—Australia ; Tasmania ; New Guinea. Dentition.—I. 7, M.4 = 12. Habits.—Strictly aquatic, frequenting banks of rivers, creeks, water-holes, and inlets of the sea. In their habits they are rather shy, and strictly nocturnal or crepuscular. Note.—This and the succeeding genus differ from all other Rodents in the paucity of their molar teeth. Their food consists of mollusks, crustaceans, and other aquatic animals, along with vegetable products. HYDROMYS. 101 1. Hypromys curysoGastEr, Geoffroy (1805). Kastern Water Rat. Fig. 4. Fig. 4.—Under surface of skull to show palate and dentition (natural size). a, Upper molars, enlarged. b, Side view of same, enlarged. Fig. 5.—Side view of skull and ramus (natural size). Fig. 6.—Lower jaw. Head, ears, back, outer surface of hind limbs, the body behind them, and the root of the tail grizzled black and buff, the former color predominating ; sides of face and body, the entire under surface, and the inner side of the limbs rich deep reddish-orange or buffy-white ; outer surface of arms deep brown ; upper surface of hind feet pale glaucous-buff, passing into brown on the tips of the toes ; basal half of tail black, apical half white. Habitat.—Eastern Australia and Tasmania, ranging at least as far northwards as the Herbert River District. References.—Gould, Mamm. Austr. iil. pls. xxiv. (H. chryso- gaster) and xxvi. (H. leucogaster); Thomas, Proc. Zool. Soc. 1889, p. 247, pl. xxix. fig. 7 (anterior zygoma-root). Note.—The two forms here mentioned, though for many years kept separate as distinct species, are now generally allowed to be mere color varieties of one species. 102 HYDROMYS. 2. Hypromys FULvoLAvaTuSs, Gould (1863). Western Water Rat. General color of fur orange-buff or buffy-brown, but the numerous black hairs which are dispersed over the upper surface give those parts a dusky hue; the whiskers, which in the other species are entirely black, are in this mixed black and white , outer surface of limbs dark brown ; upper surface of hind limbs pale brown, deepening towards the toes ; nails white ; tail black, except the extreme tip which is white. Habitat.—South and West Australia, Reference.—Gould, Mamm. Austr. iii. pls. xxv.(H. fulvolavatus ) and xxvii. (H. fuliginosus ). Note.— As with its eastern representative there are two distinct color varieties of the Western Water Rat. Mr. Oldfield Thomas apparently considers (v. Proc. Zool. Soc., 1889, p. 247) all six described forms of //ydromys to belong to one and the same species. His words are as follows: ‘One of the most singular, and at the same time the most isolated genera of Murida is Hydromys, of which the on/y species is the well-known Australian Water-rat.” According to this H. chrysogaster is the name by which the sole species should be known. Genus II.—XEROMYS, Thomas (1889). External form murine. Tip of muzzle as in J/us, not as in Hydromys. Toes unwebbed. Tail scaly, very finely haired. Skull as in Mus, except that the supraorbital edges are rounded. teeth both in number and structure as in Hydromys. Infra- orbital foramen typically murine, the outer wall broad and slightly projecting forwards. Distribution.—Queensland. Dentition.—I. i M. : SI Habits.—Terrestrial. , 1. XeRomys myoipEs, Z’homas (1889). Thomas’ Rat. External appearance like that of an ordinary Rat. Lars short and rounded, laid forward they only reach to within three or four millimetres of the posterior canthus of the eye; their anterior edge without the supplementary flap found in Hydromys. Fur very short, uniform in length. Whiskers as in J/ws, fewer and slenderer than in Hydromys. General color above dark slaty-gray, below white. Ears gray. Arms and legs like the back ; hands and feet very thinly haired, almost naked terminally, MUS. 103 white. Palms and soles naked, the former with five, the latter with six pads, the last hind pad elongate. Pollex with a short broad nail, all the other digits with claws: fifth digit on each foot without claw, reaching just to the base of the fourth. Tail about the length of the body without the head, slender, scaly, the scales rather irregularly disposed, very small, averaging about twenty to twenty-two to the centimetre, the whole tail very thinly covered with fine white hairs; its substance pale flesh color above and below. Palate-ridges as in Hydromys, i.e. three predental, the third notched in the centre, three interrupted inter- dental ridges, and one uninterrupted posterior ridge. Mamme 0-2=4. Upper incisors long, less curved than in Mus, their front surfaces smooth, ungrooved, and orange in color: lower incisors very long, their front surfaces white. Habitat.—Port Mackay, Queensland. Dimensions.— 2 ad. Head and body about four and a half inches ; tail about three and a half inches. References.—Thomas, Proc. Zool. Soc. 1889, p. 247, pl. xxix. ff. 1—4 (skull), 5 (palate-ridges), 6 (anterior zygoma-root), 8 (ear), 9 (right hind foot), and 10 —12 (left upper and lower molars). Subfamily [1.—Muvrina. Rats and Mice. Molars tuberculate, at least in youth. Cheek-pouches absent. Tail scaly, more or less naked. This sub-family contains about two hundred and fifty species belonging to eighteen well defined genera. Genus ITI.—MUS, Linneus (1766). Incisors narrow, not grooved: molars small, with three series of cusps across each tooth. Incisive foramina long. Coronoid process of lower jaw well developed. yes and ears large. Fur soft, sometimes mixed with spines. Pollex with a short nail instead of a claw. No cheek-pouches. Tail long, nearly naked, with rings of overlapping scales. Distribution.—Eastern Hemisphere, except Madagascar. Dentition.—I. 7, M. 2 = 16. Mamme.—Varying from six to twenty. Habits.—Terrestrial or semiaquatic ; fossorial ; normally grani- vorous, but under pressure of hunger, or when a semidomesticated existence has been taken up—such, for instance, as in the case of the House Mouse, Mus musculus, and the Brown Rat, Mus decumanus—omnivorous. 104 MUS. Note.— This, the typical genus of the Family (RoDENT1A) is,” Mr. Oldfield Thomas writes, ‘by far the largest of the Order, and indeed of the whole Class MamMA.ia, containing not less than one hundred and twenty species spread over the whole of the Old World with the exception of Madagascar. The number of species is, on the whole, much more considerable in tropical than in temperate regions, while but few are found where the climate is excessively cold.” The following paragraph from the same pen is of more than ordinary interest, and to it we would call the attention of our northern zoologists, whose opportunities of examining the animals at different seasons and different altitudes so far exceeds ours. ‘It is an interesting fact in connection with climate that many of the species living in hot countries have their fur more or less mixed with flattened spines, and that these spines appear to be shed during the winter and to be replaced by hairs, the latter naturally affording a warmer covering for the animal than the former.” 1. Mus ruscipes, Waterh. (1840). Dusky-footed Rat. Form stout ; ears moderate ; tail equal in length to the body ; tarsi moderate ; fur very long. General color above blackish- brown with an admixture of gray ; below grayish-white. Feet brown: tail black, sparingly covered with short bristly hairs. Incisors orange. Dimensions.--Head and body to six and a half inches ; tail to four and a quarter inches. Habitat.—The entire southern half of Australia ; Tasmania ; Islands of Bass’ Strait. References.— Waterhouse, Voy. Beagle, Mamm. p. 66, pl. xxv. ; Gould, Mamm. Austr. iii. pl. i1. Note.—This Rat is partial to the neighborhood of water, frequenting the banks of streams and lagunes, swampy localities among long grass and dense brush, and swims with great ease and rapidity. 2. Mus VELLEROSUS, Gray (1847). Tawny Rat. Form stout ; ears moderate ; tail shorter than the body ; fur very long, close, and rather soft. General color above reddish- brown with interspersed whitish hairs; below paler. Feet, and tail brown, the latter with a few short bristly hairs. Incisors yellow. MUS. 105 Dimensions.—Head and body to seven and a half inches; tail to four and a half inches. Habitat.—Plains between the Murray and Glenelg Rivers, | South Australia. References.—Gray, Proc. Zool. Soc. 1847, p. 5; Gould, Mamm. Austr. iii. pl. xii. ° 3. Mus tingoxatus, Gould (1845). Plain Rat. Ears moderate ; tail longer than the body ; fur long and very soft. General color above deep slate-gray, with the tips and the longer interspersed hairs black ; below grayish-white more or less suffused with yellow; eye encircled with black. Feet rather small and white. Tail well clothed with small hairs, blackish above, white below. Dimensions.—Head and body to five and a-half inches ; tail to four and a half inches. Habitat.—Darling Downs, frequenting the open parts of the grassy plains. Reference.—-Gould, Mamm. Austr. iii. pl. xviii. 4. Mus assimixis, Gould (1857). Allied Rat. Fur soft and silky. General color above light brown, very finely pencilled with black, below grayish-buff. Feet clothed with very fine silvery hairs. Tail nearly naked, slightly longer than the body. Dimensions.—Head and body to seven and a quarter inches ; tail to six inches. Habitat.—From North-eastern Queensland to South-western Australia. References.—Gould, Mamm. Austr. iil. pl. xiii.; Collett, Zool. Jahr. ii. 1886-7, p. 838. 5. Mus mantcatus, Gould (1857). White-footed Rat. Habit medium ; ears rather large. General color above black, gradually shading into the deep gray of the under surface ; nose, fore part of the lips, stripe down the centre of the throat and chest, and all the feet, white ; whiskers deep black. Tail naked, a little shorter than the body. Dimensions.—Head and body up to seven inches ; tail up to five inches. 106 MUS. Habitat.—York Peninsula ; Mount Kosciusko. ? Reference.—Gould, Mamm. Austr. ili. pl. xvi. 6. Mus sorpipus, Gould (1867). _ Sordid Rat. Habit stout. Ears rather large. Hair rather coarse and wiry. General color above grizzled black and brown, the former prevailing on the dorsal aspect ; below grayish-buff; fore feet grayish-brown ; hind feet silvery-gray ; tail thinly clothed with extremely fine black hairs, about equal in length to the body. Dimensions.—Head and body to six and three-fourths inches ; tail to five inches. Habitat.—Darling Downs. Reference.—Gould, Mamm. Austr. ii. pl. xvii. Note.—According to Gilbert its food consists mostly of the roots of stunted shrubs, and while it is common on the plains it is also found occasionally on the banks of creeks. 7. Mus toneipiuis, Gould (1863). Long-haired Rat. Fur very long, hairy, and somewhat harsh to the touch, of a grayish-brown at the base and tawny-buff at the tip, numerously interspersed especially along the back with very long, fine black hairs ; below buffy-gray ; feet flesh color, sparingly clothed with silvery hairs. Tail thinly beset with fine, stiff, black hairs. Dimensions.— Head and body to seven and three-fourths inches ; tail to five and three-fourths inches. Habitat.—Victoria River ? Reference.—Gould, Mamm. Austr. iil. pl. xiii. 8. Mus vetutinus, Zhomas (1882). Velvet-furred Rat. Fur very tong, soft, and velvety. General color above yellowish olivaceous gray, the hairs dark slaty-gray for nine-tenths of their length, with their extreme tips yellow, and intermixed with many longer black hairs: below bluish-gray, the bases of the hairs light slate color, and the tips dirty white. ars, feet, and tail uniform dark brown. Dimensions.—Head and body up to six and a third inches ; tail to four inches. Habitat.—Tasmania. eference.—Thomas, Ann. Nat. Hist. (5) ix. 1882, p. 415, fig. 4 (front edge of anterior zygoma-root). MUS. 107 9. Mus BurtToNI, Ramsay (1887). Burton’s Rat. Fur close, thick, soft, of uniform texture, almost woolly. Ears moderate. Tail not quite the length of the body, naked. General color above uniform dull ashy-gray or mouse color, below lighter gray. Whiskers black, reaching to behind the ears. Dimensions.—Head and body—of type specimen—four- and four-fifths inches ; tail four and one-tenth inches. Habitat.—Derby, North-western Australia. feference.—Ramsay, Proc. Linn, Soc. N.S. Wales, (2) ii. p. 553, pl. xvii. figs. 1 - 3. (skull), 4 (hind foot) and 5 (fore foot). 10. Mus TERRH-REGINE, Alston (1879). Gray’s White-footed Rat. Fur stiff and harsh both above and below, most of the hairs being developed into flattened channelled spines ; many longer cylindrical hairs on the back. Tail almost naked, considerably shorter than the head and body. Whiskers mixed black and white. lars rather large, rounded, and naked. Feet very large and stout. General color above dark reddish-brown, the longer hairs black ; lips, lower parts of cheeks, all the under surfaces, and feet yellowish-white ; tail dusky, irregularly marked with yellowish patches and rings. Dimensions.—Head and body to eight and a quarter inches; tail to rather more than seven inches. Habitat.—Cape York, Queensland. References.—Gray, Proc. Zool. Soc. 1867, p. 598 (as Acanthomys leucopus); Alston, op. cit. 1879, p. 646. 11. Mus Gouxp1, Waterhouse (1840). Gould’s Rat. Ears rather large ; tail shorter than the head and body ; tarsi slender ; fur long and soft. General color pale ochreous-yellow, interspersed above with numerous long black hairs ; entire lower surfaces, the feet, and the claws, white; ears brown ; tail brown above, yellowish-white below ; upper incisors deep orange, lower yellow. Dimensions.—Head and body to four and two-thirds inches ; tail to three and a half inches. Habitat.—Southern and Eastern Australia. 108 MUS. Note.—Gould (l.c.) gives Mus greyi, Gray, in Grey’s Travels in Australia (App. ii. p. 410, 1841), as a synonym of Mus gouldi ; this, however, appears to be an error, Gray’s species being, according to Thomas and Collett, valid. 12. Mus oreyi, Gray (1841). Grey’s Rat. General color above intense reddish-brown, interspersed with long, slender, pale tipped, black hairs ; sides yellowish-brown ; lower surfaces yellowish ; feet reddish-brown ; ears nearly naked, with short grayish hairs ; tail brown, much shorter than the head and body. Dimensions.—Head and body to six inches; tail to four and three-fourths inches. Habitat.—From South Australia to North-eastern Queensland. feferences.— Waterhouse, Voy. Beagle, i. p. 67, pl. xxxiv. fig. 18 (molars); Gould, Mamm. Austr. iii. pl. xix. feferences.—Gray, Grey’s Trav. Austr. App. ii. p. 410; Collett, Zool. Jahr. ii. 1886-7, p. 837. Note.—Prof. Collett observes that this species ‘“ takes the place in houses of Mus decumanus” in the Herbert River District. 13. Mus nanus, Gould (1857). Little Rat. Fur coarse. General color above and the outer sides of the limbs brown, with numerous interspersed fine black hairs ; below grayish-white, becoming lighter and forming a conspicuous patch beneath the tail ; feet light brown ; base of the fur bluish-gray ; tail brown, shorter than the head and body. Dimensions.—Head and body to four inches ; tail to three and a fourth inches. Habitat.—West Australia. Reference.—Gould, Mamm. Austr. ili. pl. xx. 14. Mus ALBocInEREUS, Gould (1845). Grayish-white Mouse. Habit rather stout ; ears moderate ; tail nearly equal in length to the head and body ; tarsi very slender ; fur very long and soft. General color pale ashy-gray, with a slight brownish tint on the hinder part of the back ; below white with a faint grayish tinge ; head grayish-white, pencilled with black ; feet and tail white, the latter with scattered black hairs above. MUS. 109 Dimensions.—Slightly larger than Mus musculus. Habitat.—West Australia. | References.—Gould, Mamm. Austr. iii. pl. xxi. Note.—Gould remarks: “This pretty little Mouse inhabits the sandy districts bordering the sea-shore, particularly those at the back of the sand-hills to the northward of Freemantle.” 15, Mus Nov4&-HOLLANDI#, Waterhouse (1842). Common Field Mouse. Tail not nearly so long as the head and body. Tarsi rather long and slender ; fur rather long and very soft. General color above deep gray, tipped with brownish-yellow ; below less deep gray, tipped with white ; tail dusky above, white below. Dimensions.—Head and body to three inches; tail to two inches, Habitat.—New South Wales. References.—Waterh., Proc. Zool. Soc. 1842, p. 146; Gould, Mamm., Austr. iii. pl. xxii. 16. Mus pDELicatuuus, Gould (1842). Pigmy Mouse. Ears small; tarsi delicate; tail slender, nearly as long as the head and body ; fur soft and short. General color above pale yellowish-brown ; sides delicate yellow ; lower part of the sides of the muzzle, entire under surfaces, and feet, white; fur of uniform color on the throat and mesial line of the abdomen. Dimensions.—Head and body to two and a half inches ; tail to two and a fourth inches. Habitat.—Port Essington. Reference.—Gould, Mamm. Austr. iii. pl. xxiii. 17. Mus tompsoni, Ramsay (1881). Tompson’s Rat. . Tail longer than the head and body ; fur above rather harsh, below soft. Genera) color above light gray, with a fulvescent tinge, pencilled with black ; whiskers long and black, some near the angle of the mouth white ; lower surfaces pure white ; hands rather small, gray above; feet and claws white ; tail blackish, the hairs very short. Dimensions.—Head and body to six and two-thirds inches; tail to seven and a half inches. Habitat.—Interior of New South Wales. Reference.—Ramsay, Proc. Zool. Soc. N.S. Wales, vi. p. 763, figs. 1 (pinna), 2 (wnder surface of hand) and 3 (ditto of foot). 110 MUS. Note.—Dr. Ramsay is undecided as to whether this species should be placed in the genus Mus or in Hapalotis (Conilurus of this work). 18. Mus arcurus, Zhomas (1889). White-tailed Rat. Tail rather longer than the head and body. Ears rounded, reaching just beyond the middle of the eye when laid forward. General color above pale sandy-rufous, the hairs slate-colored basally ; muzzle and underside of body white, the hairs of the chest and belly rufous basally ; hands and feet pure white ; tail wholly white, more thickly clothed than usual, the tip slightly pencilled. Dimensions.—Head and body to three and a third inches; tail to four inches. Habitat.—South Australia. Reference.—Thomas, Ann. Nat. Hist. (6) ili. 1889, p. 433, fig. p. 434 (upper molar teeth ). Note.—As in the case of Dr. Ramsay’s species just described, Mr. Thomas was undecided as to the exact position to which to assign this curious form; he remarks: “ Mus argurus has the external characters and the skull of JMZ/us, with the molars of Hapalotis ; and I am somewhat in doubt as to which of the two it should be put into. It seems indeed probable that the charac- ters of these two genera will be found so to blend together in the different species as to necessitate their ultimate union, notwith- standing the very striking characters presented by the more typical species of Hapalotis.” The following eight forms of Jfws, which have been described by Messrs. Higgins & Petterd from Tasmania, are here introduced for the sake of comparison with southern continental species, as it is impossible for the writer with the data to hand to form an opinion as to their validity or otherwise. It is not, however, at all probable that the small island of Tasmania should possess no less than eleven indigenous species of Jus, while but seventeen have been described from Australia, one only being common to both islands. 19. Mus eriseocaRuLeEvs, H. & P. (1882). Blue Rat. Ears naked and moderately long ; tail shorter than the head and body, sparsely clothed; fur long. General color above bluish-gray, sides and below ashy-gray ; feet clothed with short yellow hairs, tail with short stiff black hairs, MUS. 111 Dimensions.—Head and body to seven and a half inches ; tail to six and three-fourths inches. Habitat.— Northern Tasmania. Reference.—Higgins & Petterd, Proc. Roy. Soc. Tas. 1882, p. 173, with plate, figs. 2, 2a. 20. Mus teucorus, H. & P. (1882). Short-tailed Rat. Ears long ; tail very much shorter than head and body ; fur long and soft. General color above dark brown tipped with pale fulvous-brown, below dirty ashy-gray ; snout gray, the extreme tip nearly white; ears clothed with almost black hairs ;. tail above with short dark hairs mixed with paler, below with white hairs ; feet white. Dimensions.—Head and body to five and three-fourths inches ; tail to three and three-fourths inches. Habitat.—Northern Tasmania. Reference.—Higgins & Petterd, Proc. Roy. Soc. Tas. 1882, p. 174, with plate, figs. 4, 4a. Note.—Should this prove to be a good species the name will require to be altered. 21. Mus variaBiLis, H. & P. (1882). Swan’s Rat. Ears rather large, broad, very much rounded above, and almost naked ; tail equal in length to the head and body ; fur rather long and soft. General color above dark bluish-gray or fawn, below pale bluish-gray or white; feet brownish, fawn color, or white ; tail dark brown. Dimensions.— Head and body to eight inches ; tail to the same length. Habitat.—Tasmania (St. Leonards). Reference.—Higgins & Petterd, Proc. Roy. Soc. Tas. 1882, p. 174, with plate, figs. 3, 3a. 22. Mus simsoni, H. & P. (1882). Simson’s Rat. Ear moderately long; tail longer than the head and body, thickened at the base. General color above grayish-brown inter- spersed with darker hairs, paler below ; face bluish-gray ; chin white ; ears brown ; feet yellowish-white ; tail pale brown. 112 MUS. Dimensions.—Head and body to two and five-eighths inches; tail to two and seven-eighths inches. Habitat.—Tasmania (Ringarooma). Reference.—Higgins & Petterd, Proc. Roy. Soc. Tas. 1882, p. 175, with plate, figs. 5, 5a. 23. Mus pacuyurus, H. & P. (1883). Thick-tailed Rat. Ear moderate, rounded ; tail thick, sparsely clothed, much shorter than the head and body ; fur moderately long and rather soft. General color above dark brown, below paler, especially behind, where it is grayish-brown. Fore feet thickly clothed with long brown hair, hind feet moderately so ; tail brown. Incisors yellow at the tip, white at the base. Dimensions.—Head and body to six and three-fourths inches ; tail to four and one-eighth inches. Habitat.—Tasmania (Long’s Plains). Reference.— Higgins & Petterd, Proc. Roy. Soc. Tas. 1883, p. 182, with plate, figs. 1 - 10. Note.—The molar teeth, if correctly figured, would necessitate the exclusion of this animal from the genus J/us as now restricted. 24. Mus castaneus, H. & P. (1883). Chestnut-colored Rat. Form very robust. Ears broad and roundly pointed; tail much shorter than the head and body ; fur very long, dense, and soft. General color above chestnut, interspersed with longer black hairs, below yellowish-ash ; nose, chin, and throat leaden- gray ; fur on the cheeks excessively long and bushy ; tail brown above, lighter below ; hands and feet leaden-gray. Upper incisors orange, lower yellow. Dimensions.—Head and body to six and three-fourths inches ; tail to four and three-eighths inches. Habitat.—Tasmania (Long’s Plains). Reference.—Higgins & Petterd, Proc. Roy. Soc. Tas. 1883, p. 185, with plate, figs. 2 - 20. ; 25. Mus ramarensis, H. & P. (1883). Tasmanian Water Rat. Ears rounded ; tail a trifle shorter than the head and body ; fur somewhat coarse and moderately long. General color above CONILURUS. 113 mottled yellowish-brown, below grayish-white ; a dark patch at the anterior portion of the base of the ear; fore feet grayish-white, hind feet and toes long and slender, pure white ; tail brown above, grayish-white below, with the tip almost black. Dimensions.—Head and body to six and three-fourths inches ; tail to six and a half inches. Habitat.—Northern Tasmania. Reference.—Higgins & Petterd, Proc. Roy. Soc. Tas. 1883, p. 185. Note.—The authors of the species state that M. tamarensis is “extremely abundant on the banks of the river Tamar, and probably widely distributed over the island. Settlers residing near the river suffer much from its destructive propensities.” In a later paper by the same authors describing yet another new Tasmanian species of Jus, a list of the “ Terrestrial Animals of Tasmania” is given. From this list the name of IL tamarensis is omitted, although no comment is made by the authors on the reason for the excision of this their iatest species. 26. Mus Tetraconurvus, H. & P. (1883), Quadrangular-tailed Rat. Form stout ; ears short and broadly rounded ; tail short, quadrangular ; fur very long and soft. General color above dark ashy-gray, thickly interspersed with longer blackish hairs ; lips and entire under surface slaty-gray ; hands and feet ashy-gray ; tail brown. Dimensions.—Head and body to six inches ; tail to less than four inches. Habitat.—Tasmania. Reference.—Higgins and Petterd, Proc. Roy. Soc. Tas. 1883, Par Lo. Genus IV._CONILURUS, W. Ogilby (1838). Hind limbs more or less elongated. Incisive foramina very large. No coronoid process to the lower jaw. Ears and tail long. Distribution.— Australia. Dentition.—I. 3, M.2 x 2 = 16. Note.—I have been reluctantly obliged to abandon the better known name /apalotis (Lichtenstein, 1829), in favor of the above, proposed by my father, since the former name was used by Hiibner in 1816 for a genus of Lepidopterous insects, and H 114 CONILURUS. cannot, therefore, be utilized again. The species on which the genus Conilurus was founded was named by its describer C. constructor, but further researches have proved its identity with the Hapalotis albipes of Lichtenstein. Major Mitchell’s original specimens were forwarded to the British Museum under the name of ‘Native Rabbit,” and the generic term selected above is intended to signify a “small rabbit with a long tail.” These graceful little animals supply in Australia the place of the Jerboas of Africa, South-eastern Europe, and Southern and Central Asia. 1, ConILuRUS ALBIPES, Lichtenstein, sp. (1827). White-footed Jerboa-Rat. Tail equal in length to the head and body or but little shorter ; fur long, soft, and close. Upper surface of the head and body, the ears, flanks, and outer surface of the limbs gray, tipped with ashy-brown, interspersed with numerous fine black-tipped hairs ; whiskers and a narrow band encircling the eye black ; under surface of body, inner surface of limbs, hands, and feet white ; tail above dark brown, sides, below, and extreme tip white. Dimensions.—Head and body to ten inches ; tail about the same length. Habitat.—South-eastern Australia ; southern portion of South Australia. References.—Ogilby, Trans. Linn. Soc. 1838, xviii. (description) p. 126, as C. constructor ; Gray, Ann. Nat. Hist. ii, 1839, p. 308; Gould, Mamm. Austr. iii. pl. i. Note.—According to Gould this species, though widely dis- persed within the limits indicated above, is nowhere very abun- dant. It is “strictly nocturnal in its habits, sleeping during the day in the hollow limbs of prostrate trees, or such hollow branches of the large Hucalypti as are near the ground, in which situations it may be found curled up in a warm nest of dried leaves.” Fossil remains of this species have been obtained in the Pleistocene of New South Wales. The following remarks from the pen of Sir George Grey touch- ing the method of carrying its young, adopted by this species and possibly by others of its congeners, but so totally at variance with the habits prevailing in the intimately allied genus Mus, are worthy of reproduction ; he writes, ‘The specimen I send you, a female, had three young ones attached to its teats when it was caught: the mother has no pouch, but the young attach them- selves with the same or even greater tenacity than is observable in the young of Marsupiata (Meraruerta of this Hand-list, Hu CONILURUS. 115 vide p. 4). “While life remained in the mother,” he continues, “they remained attached to her teats by their mouths, and grasped her body with their claws, thereby causing her to present the appearance of a Marsupial minus the pouch. On pulling the young from the teats of the dead mother, they seized hold of my glove with the mouth, and held on so strongly that it was diffi- cult to disengage them.” Should the above account be correct,—and with an observer whose veracity and accuracy are unquestionable, there can be no reason for doubting the statement,—and should the same habit be common to all, or even some, members of the genus,—I have failed to elicit any further information on the subject, either confirmatory or rebutting, from experienced zoologists and col- lectors—it raises the question whether Conilurus, a genus purely belonging to, and even in a fossil state so far confined to, con- tinental Australia, may not originally have been a marsupial Rodent, which is even now in a transition stage between the Metatherian and Eutherian types. The fact of Thomas’ Mus argurus having such close affinities (vide p. 110) to both genera, that even that talented writer is unable to say for certain to which genus this South Australian mammal belongs, would seem to strengthen the position here put forward. The discovery also by Dr. Stirling of the so-called ‘“ Marsupial Mole” (Notoryctes ), a form, which some of the foremost scientists of the age consider to be closely allied to the South African Golden Mole (Chryso- chloris), and in which the pouch is aborted or at the least rudimentary, again points to a gradual supersession of the older marsupial forms, and their immergence with the more recent and more highly developed monodelphian type. 2. ConILURUS MACRURUS, Peters, sp. (1876). Peters’ Jerboa-Rat. Ears large and rounded ; tail much longer than the head and body ; fur soft. General color above reddish-brown, intermixed with scattered longer black hairs ; below white ; ears rust-colored ; feet clothed with short white hairs: proximal fourth of the tail brown, clothed with short scattered bristles ; the rest densely covered with gradually lengthening white hairs, which at the tip exceed an inch in length. Dimensions.—Head and body to eight and a quarter inches; tail to twelve and a half inches. Habitat.—North-western Australia. Reference,—Peters, Mon. Ak. Berl. 1876, p. 355, plate, p. 366, 116 CONILURUS. 3. CoNILURUS BOWERI, Ramsay, sp. (1886). Bower's Jerboa-Rat. Ears small, with the tips rounded, and almost naked ; tail longer than the head and body. General color above light gray, pen- cilled with long black hairs; a broad, distinct, irregular, median band, rufescent on the nape and basal inch of the tail, golden- brown on the intervening portions ; next two inches of tail blackish, the rest white, terminating in a well defined brush ; under surfaces and feet white. Dimensions.—Head and body up to eleven inches ; tail to about thirteen inches. Habitat.—North-western Australia. Reference.—Ramsay, Proc. Linn. Soc. N.S. Wales (2) i. 1886, p. 1153, pl. xviii. Note.—This species is very closely allied to the preceding ; in fact, if it were not for the difference in the comparative dimen- sions of trunk to tail, I should have no hesitation in considering them identical. 4, CONILURUS APICALIS, Gould, sp. (1851). White-tipped Jerboa-Rat. General color above pale brown, interspersed with numerous fine black hairs ; below white ; face and sides of neck bluish-gray ; flanks mixed gray and buffy-white ; fore feet white with a dark brown spot on the fore-arm, hind feet and tarsi white ; proximal three-fourths of the tail brown, the remaining portion thinly clothed with white hairs. Dimensions.—Head and body to eight inches ; tail to eight and a half inches. Habitat.—South Australia. Reference.—Gould, Mamm. Austr. iil. pl. i. Note.—This species has been found in a fossil state in the Pleistocene of New South Wales. 5, CoNILURUS HEMILEUCURUS, Gray, sp. (1857). Hilsey’s Jerboa-Rat. Ears short ; tail shorter than the head and body; fur harsh and wiry. General color above light sandy-brown, with numerous scattered fine long black hairs ; below buffy-white, the feet, fore- arms, and tarsi even lighter; basal portion of the tail brown, deepening into black about the middle, beyond which it is white with a short apical tuft. CONILURUS. 117 Dimensions.—Head and body up to eight inches; tail to six and a half inches. Habitat.—Central Queensland. Reference.—Gould, Mamm. Austr. iil. pl. ili. 6. ConiLuRUs HIRSUTUS, Gould, sp. (1842). Long-haired Jerboa-Rat. Tail much longer than the head and body; fur coarse and . shaggy. General color above yellowish-brown with very numerous longer interspersed black hairs ; below rusty yellow tinged with brown on the neck and chest ; feet black, the claws whitish ; basal three-fourths of tail black, the remainder rusty white, the apical tuft exceeding an inch in length. Dimensions.—Head and body up to ten and a third inches; tail to thirteen inches. Habitat.—Northern Queensland. References.—Gould, Proc. Zool. Soe. 1842, p. 12, and Mamm. Austr. iii. pl. iv. 7. ConILURUS PENICILLATUS, Gould, sp. (1842). Black-tailed Jerboa-Rat. Tail slightly longer than the head and body ; fur rather spiny. General color above grayish-brown grizzled with buff, the occiput and neck tinged with rusty ; entire under surfaces, inner surfaces of the legs, and the feet white with a faint yellow tint ; apical half of the tail black and moderately tufted. Dimensions.—Head and body up to seven and a quarter inches ; tail to seven and three-fourths inches. Habitat.—Northern Queensland. References.—Gould, Proc. Zool. Soc. 1842, p. 12, and Mamm. Austr. i. pl. v. Wote.—Writing of the habits of C. penicillatus, Mr. Gilbert (vide Gould) remarks, “this little animal is only seen on the beach where there are large Casuarina trees, in the dead hollow branches of which it forms a nest of fine dry grass, and retires during the day ; in the evening it leaves its retreat and proceeds to the beach, where it may be seen running along at the edge of the surf as it rolls up and recedes, apparently feeding upon any animal matter washed up by the waves.” Personally Gould states that “its habits would seem to be somewhat singular, inasmuch as it is frequently found among the swamps on the sea-shore ; I have no evidence, however, that it 1s not also found in the interior of the country.” 118 CONILURUS. 8. CoNILURUS PERSONATUS, Krefft, sp. (1867). Krefft’s Jerboa-Rat. Tail much shorter than the head and body ; fur coarse. General color above reddish-brown, below sandy white; a black mark surrounding the eye and continued along the side of the snout. Tail covered with coarse irregular scales, between which a few stiff hairs are visible. Dimensions.—Head and body up to nine inches ; tail to six and a half inches. Habitat.—Northern Queensland. Reference.—Krefit, Proc. Zool. Soc. 1867, p. 318. 9. ConiLuRUS conpITOR, Gould, sp. (1849). Nest-building Jerboa-Rat. Ears large; tail equal in length to the head and naa ;far soft and silky. General color above grayish-brown, darkest down the middle of the head and back ; below pale buff; hands brown ; feet very large, pale brown ; tail brown above, paler beneath. Dimensions.—Head and body six inches. Habitat.—Interior of Eastern Australia. References—Ogilby, Trans. Linn. Soc. 1838, xviii. p. 127 (habits) ; Gould, in Sturt’s Exped. into Centr. Austr. i. p. 120, and ii. App. p. 7, and Mamm. Austr, iii. pl. vi. Note.—This species has received its specific name from its habit of constructing a large nest in which one or more families dwell ; in the latter case, however, each family occupies a separate compartment, but with a passage communicating between them ; these nests are built of small sticks, and are so firmly put together as to defy the attacks of a dog. The nests are somewhat in the form of a beehive, with a diameter of about four feet and a height of about three, and the method of construction is thus described by Major Mitchell: ‘“ For this purpose the little animal chooses some small bush or shrub as a fixed point dappui to commence its operations ; and by gradually working round this, and interlacing the materials of its fortalice, first of all with the growing branches of the centre bush, and afterwards with one another gradually extends it to the enormous dimensions speci- fied.” The inhabited compartments are warmly lined with grass. 10. ConiLuRUS mURINUS, Gould, sp. (1845). Mouse-like Jerboa-Rat. Ears large. Tail much shorter than the head and body ; fur remarkably soft and delicate. General color above delicate CONILURUS. 119 ochraceous-yellow with a considerable admixture of black ; below butfy-white, as also are the hands and feet ; tail moderately clothed, above mixed black and white, below pure white. Dimensions.—Head and body up to five and a half inches ; tail to three and three-fourths inches. Habitat.—Interior of New South Wales and South Australia. Reference.—Gould, Mamm. Austr. iii. pl. vii. 11. ConILuRUS LONGICAUDATUS, Gould, sp. (1844). Long-tailed Jerboa-Rat. Ears large and naked. Tail much longer than the head and body ; fur close and very soft. General color above pale sandy, intermixed with numerous fine black hairs, which are longest posteriorly ; below white ; ears dark brown ; feet and tarsi white ; basal half of the tail clothed with short dark brown hairs, apical half with longer black hairs tipped with white, the extreme tip white. Dimensions.—Head and body up to seven inches; tail to nine inches. Habitat.—Interior of Western Australia. Feferences.—Gould, Mamm. Austr. iii. pl. viii. Note.—Gould on the authority of Gilbert states that ‘the favorite haunt of this species is a stiff and clayey soil. It is also very partial to the mounds thrown up by SBettongia grayr (B. lesueurt of this work) and Peragale lagotis. It is less des- tructive to the sacks and bags of the storerooms, but, like H, mitchellt, is extremely fond of raisins.” 12. CoNILURUS MITCHELLI, Ogilby, sp. (1838). Mitchell’s Jerboa-Rat. Ears moderate, naked, and somewhat pointed ; tail longer than the head and body ; fur close and very soft. General color above very pale sandy, intermixed with fine black hairs which are longest posteriorly ; sides of face, under surface, inner side of the limbs, and the feet grayish-white ; a broad patch down the middle of the throat and chest pure silky white ; ears dark brown ; upper surface of the tail dark brown, and crested towards the tip ; lower surface white. Dimensions.—Head and body up to four and three-fourths inches ; tail to six inches. Habitat.—South and West Australia. 120 CONILURUS. References.—Ogilby, Proc. Linn. Soc. 1838, xviii. p. 1380 ; Gould, Mamm. Austr. iu. pl. ix. Type.—In the Australian Museum. Note.—Gould remarks that this species differs from the pre- ceding in preferring sandy districts, frequenting the sides of grassy hills tolerably well clothed with small trees growing in a light soil, in which it forms its burrow. 13. ConiLurus cERVINUS, Gould, sp. (1851). Fawn-colored Jerboa-Rat. Ears very large, pointed, and nearly naked ; tail longer than the head and body. General color above delicate fawn inter- mixed with numerous fine black hairs; nose and under surfaces white ; tail pale brown above, lighter below. Dimensions.—Head and body up to four and a half inches ; tail to five and a half inches. Habitat.—Interior of South Australia. Reference.—Gould, Mamm. Austr. iii. pl. x. Genus V.—MASTACOMYS, Thomas (1882). Similar to Mus, but with the molars remarkably broadened and the mammez reduced in number to four. 1. Masracomys Fuscus, Z’homas (1882). Broad-toothed Rat. Ears rather large ; tail shorter than the head and body; fur extremely long and soft. General color both above and below dark grayish-brown ; tail and upper side of feet clothed with dark brown hairs, those on the former not lighter below. Sole-pads five on the fore and six on the hind feet. Molars remarkably broad and heavy, the anterior ones each more than half as broad again as the palatal space between them ; middle lamina of the first molar and anterior lamina of the second with three cusps ; the additional ones external and very small. Dimensions.—Head and body up to five and three-fifths inches ; tail to three and three-fourths inches. Habitat. —Tasmania. Reference.—Thomas, Ann. Nat. Hist. (5) ix. p. 413, figs. 1 (inner view of upper jaw, &c.), 2 (molars), and 3 (front edge of anterior zygoma-root ). Note.—Fossil remains of this Rat have been obtained from the Wellington Caves, New South Wales. UROMYS. 121 Genus VI.—UROMYS, Peters (1867). Differs from J/us in having the scales of the tail not over- lapping, but set edge to edge, so as to form a sort of mosaic work. Distribution.—From Eastern Australia to the Aru Islands. 1. Uromys maAcropus, Gray, sp. (1866). Giant Rat. Ears moderate ; tail equal to or a little shorter than the head and body ; fur moderately soft, the long hairs rather bristly. General color above grayish-brown tinged with reddish, with coarse black-tipped hairs intermixed ; below white; whiskers very long, stiff, and black; feet white ; tail black on the basal, white or pale yellow on the apical half. , Dimensions.—Head and body up to fourteen and a half inches; tail to about the same length. Habitat.—North-Eastern Australia. Reference.—Gray, Proc. Zool. Soc. 1866, p. 221, and 1867, p- 597; Krefft, Proc. Zool. Soc. p. 316, figs. 1-7 (skull) ; Peters, Mon. Ac. Berl. 1867, p. 344 (animal, skull, and feet jigured ). 2. URoMYS CERVINIPES, Gould, sp. (1852). Buff-footed Rat. Fur short, soft, and adpressed, without lengthened hairs. General color of adult: above sandy-brown, below mottled bufty- white and gray ; feet and tarsi fawn color; tail purplish-flesh color. Young bluish-gray above, grayish-white below. Dimensions.—Head and body about six inches ; tail about five and a half inches. Habitat.— Eastern Australia. Reference.—-Gould, Mamm. Austr. i. pl. xiv. In 1867 Gray (Proc. Zool. Soc. p. 599) described, under the name of Hchiothrix leucurus (lege Echinothrix leucura) a remark- able Rat, having an extremely elongated muzzle, supposing it to have come from North Australia; it is now believed to be confined to the Celebes, whence only has it since been recorded. Numerous fossil Murine remains have been obtained in various parts of Australia, chiefly in the Wellington Caves, but no systematic attempt has been made as yet to work these out. 122 CARNIVORA. Order V.-CARNIVORA. Unguiculate Mammals with never less than four well developed toes on each foot, all of which are usually clawed. Pollex and hallux never opposable to the other digits. Dentition diphyodont and heterodont, the teeth always rooted, consisting, in each ramus, of generally three incisors, the outer one being always the largest ; of a strong, conical, pointed, recurved canine, and of a variable but usually more or less compressed, pointed, and trenchant series of molars. Brain never destitute of well marked convolutions. Stomach simple. Cccum absent or short and simple. Mamme abdominal and variable in number. Clavicle often entirely absent, and when present never complete. Habits.—Carnivorous and sanguivorous, sometimes omnivorous. Suborder I.—Fissipedia. Carnivores fitted for a terrestrial or mainly terrestrial pro- gression and mode of life. Incisors almost always % on each side. In the molar series there is always one specially modified tooth in each ramus, which is termed the ‘sectorial ” or ‘“ flesh-tooth,” and is usually enlarged ; in the upper this tooth is the last pre- molar, in the lower the first molar. Group—CYNOIDEA. Head elongate ; tail moderate or rather long ; limbs fairly developed, the feet digitigrade. Fore toes, except in the African genus Lycaon, five, the pollex, however, being short and non- functional; hind toes in all wild species four. Claws blunt, nearly straight, and non-retractile. Organs of scent, sight, and hearing highly developed. Auditory bulla much dilated, rounded, and subdivided. Paroccipital process flattened against the bulla and projecting behind. Condyloid and glenoid foramina distinct. Ceecum elongate and generally folded on itself. Clavicles rudi- mentary. Vertebre.—C. 7, D. 13, L. 7, 8..3, Cd. 17 = 22. Habits.—Carnivorous, but some, especially of the smaller forms, are omnivorous. Many of the species, such as the Wolf and the Cape Hunting Dog, are gregarious and hunt in packs, others, as for instance the Fox, hunt singly or at most in pairs, and show extraordinary cunning both in avoiding danger to themselves and in securing their prey ; many are fossorial. Note.—Prof. Huxley has divided this Group into two parallel series, the Thooid or Lupine forms and the Alopecoid or Vulpine forms, characterised by the presence of frontal air-sinuses in the CANIS. 123 former, which not only affect the external contour but to a still greater degree the shape of the anterior part of the cranial cavity. It is to the first of these series that the Australian species belongs. Thooid forms are not found in Africa or South America. Family IL—CANID. Characters similar to those of the Group of which this is the only family. Genus I.—CANIS, Linneeus (1766). Pupil, when contracted, round in some species, elliptical and vertical in others. Limbs of moderate proportions. Tail gener- ally forming a moderate brush. Mamme generally ten, more rarely eight. Teeth powerful. Dentition.—I. 4, C.i, P. 4, M.% x 2 = 42. Flower and Lydekker (Introduction to the Study of Mammals living and extinct, p. 546) remark: ‘‘The absence of the last upper molar (m *) alone distinguishes this from the generalised dentition of heterodonts, and this tooth is occasionally present in one species (C. cancrivorus). In certain Asiatic species (C. primevus and its allies) which on this account have been separated to form the genus Cyon of Hodgson, the last lower molar (m ,) appears to be constantly absent.” The first permanent premolar in both jaws is without a milk-predecessor, and in the upper jaw is decidedly smaller than the second. Distribution.—Cosmopolitan. 1. Canis pinco, Blumenbach (1780). Warrigal; Dingo; Native Dog. Of this too well known animal it is hardly necessary to give a description, more especially as it is the only terrestrial Carnivore existing in a wild state on Australian soil; nevertheless, the remarks of Prof. St. George Mivart on the subject may be suitably reproduced here. He writes :— “The Dingo varies in its coloration from red to black. There is a grayish underfur, but, save in the black variety, the long hairs are generally yellow or whitish. The top of the head and dorsal region generally are of a darker reddish-yellow, often intermixed with black. The underparts are paler and may be whiteish. The end of the tail is very often white, as are frequently 124 CANIS. the feet and sometimes the muzzle, though this is also sometimes black. The animal may be of an uniformly light reddish or yellowish brown, save that it is paler beneath, on the outside of the forelegs, below the elbow, as well as on the inside of the limbs and on the cheeks.” In reference to the vexed question as to whether the Warrigal is an indigene or has been brought hither through human instru- mentality, we consider, notwithstanding that the greater number of authors incline to the latter theory, that the recognition by Prof. McCoy of fossil remains, in no wise differing from those of recent individuals, and contemporaneous with similar remains of Thylacoleo, Diprotodon, &c., sets this question at rest, and goes far towards proving that this species is indigenous to continental Australia, and was an inhabitant thereof prior to its colonization by man, no human remains of such antiquity having as yet been discovered. As this question is so intimately connected with that of the origin of the domestic dog and its many varieties, no apology is needed for quoting largely from Prof. McCoy’s article (Prod. Paleont. Vict. dec. vil. pp. 7-10). He says :— “The origin of the domestic dog is a question of great difficulty and interest, which it has been suggested can be best investigated by a study of the Dog known to the lowest types of the human race ; and the aboriginal inhabitants of Australia were thought to afford these conditions. On the other hand the remarkable absence of the higher forms of Mammalian Quadrupeds in Aus- tralia was supposed to render it highly probable that the Dingo was not really a native of the place, but was brought at some remote period from some other country by human savage races arriving to constitute the population of Australia. Taking the case of the Dingo, it was certain that the native dogs of con- tinental Asia were not clearly related, to the extent of specific identity, with the Australian one, nor could any near analogies be found elsewhere ; while on the other hand the facts are beyond dispute: (1st) that the Dingo is singularly averse to domestication and man’s society when compared with other dogs ; (2nd) that it is extremely abundant, with little or no variation, over the whole of Australia; and (3rd) that the further you go from human haunts, near the coast, into the desert interior, the more numerous do the Dingoes appear, indicating that the species was a really indigenous one.” And again, alluding to its contemporaneity, mentioned above, with the great fossil Mammals of Australia, he remarks “ that the Dingo was really one of the most ancient of the indigenous mammals of the country, and abounded as now most probably before man himself appeared. . . . . Our present species, PINNIPEDIA. 125 although still living in great numbers, I have no doubt dates from the Pliocene Tertiary time, and I find, on the most minute comparison and measurements, no difference between the fossil and recent individuals, either of the adult age, or of the younger periods before the milk-teeth were shed to give place to the permanent molar teeth.” These remarks from so high an authority on Australian Zoology, having the concurrence of Prof. Mivart, cannot - be ignored, and, until proof to the contrary is forthcoming, we shall consider the honor of . being the original progenitor of our house- hold favorite as the due of the Australian Warrigal. Furthermore, Mr. R. Etheridge, jun., has kindly supplied the following note, extracted from Smyth’s Aboriginals of Victoria, i. p. 149, 1878: “Ina well section at Tower Hill, Western Vic- toria, sixty-three feet of volcanic ash was passed through, and then sixty feet of blue and yellow clay; here were found the skull and bones of the Dingo.” Again: “ At Lake Timboon, Western Victoria, bones of the Dingo were found associated with those of the Tasmanian Devil (Sarcophilus ursinus), those of Macropus titan, and bones and teeth of Diprotodon.” Suborder II.—Pinnipedia. Seals; Walruses. External form fitted for an aquatic life; limbs modified into swimming organs ; digits of the hand decreasing in length from the first to the fifth ; of the foot first and fifth largest and longest, the three middle ones subequal in length. Dentition simple, generally unspecialized, the molar series similar to each other in size and form. Habits.—More or less purely aquatic ; carnivorous, feeding on fishes, molluscs, and crustaceans, to all of which they are very destructive owing to their exceptional voracity. The develop- ment of the brain is very great, and they are, therefore, easily domesticated, becoming much attached to their keepers and readily learning various tricks ; they are also affectionate parents, and courageously defend their progeny from threatened attack. A curious habit, common to all Pinnipeds, and the reason of which is still a matter for conjecture, is that of swallowing numerous stones up to the size of a hen’s egg. Distribution.—Seas of the circumpolar and temperate regions of the Globe chiefly, only one genus (Monachus) being strictly tropical, while but few species, one of which is the Australian Zalophus lobatus, range into tropical waters. 126 GRESSIGRADA. Group I.—GRESSIGRADA. Eared Seals; Walruses, Hind limbs capable of being turned forwards, and used in terrestrial locomotion. Neck lengthened. Anterior feet nearly as large as the posterior, their digits rapidly decreasing in length from the first to the fifth, without distinct claws, and with a broad cartilaginous border extending beyond the digits. Only the three middle digits of the hind feet clawed, and all terminating jn long narrow cartilaginous flaps. Family 1.—OTARIIDA. Bared Seals. Fore limbs placed far back and comparatively free ; palms and soles and the greater part of the upper digital surface hairless. Scapula large. Ears witha subcylindrical external conch. Testes scrotal. Dentition.—I. 2, C. 7, M. 2 OF 2 x 2 = 34 or 36. Note.—The Group to which this Family belongs are gregarious and polygamous, and the males greatly exceed the females in size. During the breeding season they resort in large numbers to favorite breeding grounds, technically known to sealers as ‘‘rookeries,” where they leave the water and pass some weeks on land, often at a considerable distance from the shore ; at this period they rarely enter the water and consequently do not feed ; the males especially, on their return to what must be considered their natural element, are greatly emaciated. Genus I.—ZALOPHOUS, Gill (1866). Molars %, large, closely approximated, the last under the hinder edge of the zygomatic process of the maxillary. Muzzle narrow. Hinder edge of the palatine bones deeply concave. Sagittal crest, in very old males, forming a remarkably high, thin, bony plate, unparalleled in its great development in any other genus in the Family. 1. ZALOPHUS LOBATUS, Gray, sp. (1828). Australian Sea Lion. In the adult the face, front and sides of the neck, all the under surface, sides, and back dark- or blackish-brown, passing into dark slaty-gray on the extremities of the limbs ; the hinder half of the crown, the nape, and back of the neck rich deep fawn color ; eyes black. ARCTOCEPHALUS. 127 Dimensions.—Adult males up to ten feet; females much smaller. Habitat.—South and West Australia ; Japan. References.—Gould, Mamm. Austr. iii. pl. xlix.; Quoy & Gaimard, Voy. Astrolabe, Zool. i. p. 95, Atlas, 1833, pls. xiv., xv. Note.—Gilbert, writing to Gould, says, speaking of some thirty years ago: “This animal is extremely numerous on all the low islands of the Houtmann’s Abrolhos, particularly those having sandy beaches ; but it does not confine itself to such places, being often found on the ridges of coral and madrepores, over which we found it very painful walking, but over which the seals often outran us. On many of the islands they have been so seldom (perhaps, indeed, never before) disturbed, that I frequently came upon several females and their young in a group under the shade of the mangroves; and so little were they alarmed, that they allowed me to approach almost within the reach of my gun, when the young would play about the old ones, and bark and growl at us in the most amusing manner ; and it was only when westruck at them with clubs that they shewed any disposition to attack us or defend their young. The males, however, would generally attack the men when attempting to escape ; but, generally speak- ing, the animal may be considered harmless, for even after being disturbed, they seldom attempt to do more than take to the water as quickly as possible.” In the Prodromus of the Paleontology of Victoria (dec. v. pls. xli., xlii.) Prof. McCoy figures, under the name of Areto- cephalus williamsi, a fossil Seal from the Pliocene of Victoria obtained at Queenscliff and Cape Otway. Referring to this Allen remarks: ‘“ The skull figured, which he (2.e. McCoy) refers to as an ‘old male skull’ bears a close resemblance to the skull of a female of Zalophus lobatus, from which, judging from his description and figures, it does not very materially differ. Genus II.—ARCTOCEPHALUS, F. Cuvier (1824). Molars 2, triangular, pointed, and compressed, the last entirely behind the hinder edge of the zygomatic process of the maxillary. Muzzle slender, elongated, and pointed. 1. ARCTOCEPHALUS FORSTERI, Lesson, sp. (1828). Australian Sea Bear. In the adult male the entire upper surfaces are dark brown, the belly, limbs, tail and lips chestnut ; the female is of a gener- ally lighter coloration, The young are blackish-brown above, with the muzzle and throat yellowish, and the belly rust color. 128 REPTIGRADA. Dimensions.—Adult males up to eight feet ; females to five and a half feet. Habitat.—Southern and South-eastern Australia; New Zea- land; Falkland Islands. References.—Quoy & Gaimard, Voy. Astrolabe, Zool. i. p. 89, Atlas, pls. xil., xiii andxv. ; McCoy, Prodr. Zool. Vict., decs, iv. pl. xxxi. and viii. pl. 1xx1. Note.—Referring to the islands in Bass’ Straits, where these animals are still plentiful, the following extracts taken from Prof. McCoy’s later article (dec. vii.) on the subject, will be read with interest : ‘“‘The Seals come to the Rocks about the Ist of October. The time of bringing forth the pups is between the 10th of November and the 10th of December. They do not commence to breed until they are three years old. The male during the pupping season will ascend the rocks and remain for one or two months without food, and is extremely attentive to the female and pups. The cow generally brings forth one pup, sometimes two.” Group II.-REPTIGRADA. Harless Seals. Hind limbs incapable of being turned forwards, and not ser- viceable for terrestrial locomotion. Neck short. Anterior feet smaller than the posterior, the first digit little, if any, longer than the next succeeding ones, all armed with strong terminal claws. All the digits of the hind feet usually armed with strong claws, and without terminal cartilaginous flaps. Family I1.—PHOCID/:. Farless Seals. Fore limbs placed well forward. Hands and feet hairy. Scapula small. No external ear. Testes enclosed within the body. Jote.—The Earless Seals are monogamous, and there is no marked variation in size between the sexes. With the exception of the Sea Elephants (JMacrorhinus), which in their habits during the season of reproduction resemble the Otariide, by assembling in large numbers at well known resorts, these Seals do not so uniformly resort to particular breeding grounds on land, but, being confined almost entirely to the colder latitudes, usually bring forth their young on the ice, and leave the water only for short periods ; they are, however, as a general rule social in their habits and possessed of great affection for their young. A single OGMORHINUS. 129 calf only is commonly brought forth, and the period of gestation is said to range from nine to nearly twelve months. Seals are greatly attracted by musical sounds, and in one instance the writer can personally vouch for a Seal /Phoca vitulina), which, by the simple medium of whistling was induced to follow his boat to and from the fishing grounds for several days in succession, the animal frequently rising within an oar’s length of the boat ; strange to say it never attempted to seize any of the fish (mostly Cod and Ling) as they came up on the hook, though it was seen to hunt the small Sharks (Acanthias vulgaris and Galeus vulgaris ) which at that season infested the waters ; this occurred on the North Coast of Ireland. The food of Seals does not consist so greatly of fishes as is generally supposed, molluscs, crustaceans, and medusz being staple articles in their diet, with an occasional bird thrown in asa bonne bowche. Some species, such as the Bearded Seal (Hrignathus barbatus ), and the Ringed Seal (Phoca fetida), neither of which are to any extent migratory, are said to feed almost exclusively on small crustaceans, chiefly of the genus Gammarus. Various theories have been adduced as to the remarkable power which permits these warm-blooded, air-breathing mammals to remain under water for the space of, according to different authorities, from eight to twenty minutes, but, Mr. Allen pro- perly remarks, “ none of these theories seem satisfactory.” Genus II].—OGMORHINUS, Pefers (1875). Molar teeth separated from one another, with distinct pointed cusps, the middle cusp being the largest and slightly recurved. Muzzle compressed and elongated. Dentition.—I. 3 C. ES M. 2 x 2 = 32. Note.—F. Cuvier’s name, Stenorhynchus, having been pre- viously employed by Latreille for a genus of Coleopterous Insects, it becomes necessary to adopt the term proposed by Dr. Peters. 1. OamorHINUS LEPTONYX, Blainville, sp. (1820). Sea Leopard. Above ashy-gray with large spots and patches of yellowish- white, or greenish-gray shading into creamy-white on the sides which are blotched and spotted with black. Throat and belly grayish- or yellowish-white, with or without small dark spots. Dimensions.—Total length up to ten feet ; sexes not markedly different in size. {I 130 OGMORHINUS. Habitat.— Antarctic Ocean, occasionally straggling as far north as the southern shores of Australia and New Zealand ; Lord Howe Island. References.—Gray, Voy. Erebus & Terr. Mamm. p. 4, pls. iil. iv.; Gould, Mamm. Austr. iii. pl. 1.; McCoy, Prodr. Zool. Vict. dec. iii. pl. xxi. tr BSc oy! | Jo gel Se Species not represented in the Australian Museum are marked * against their names in the Index. PAGE *abramus (Vesperugo) 89 acetabulum a 500 sen XV Acrobates 24, 36 acromion ... .»-Xiil. aculeata (Echidna) fe 3, 4 adversus (Vespertilio)... EASE ipyprymnus cet . 43 *affinis (Tiaphozous) 96, 97 Agile Wallaby . a we 54 agilis (Macropus) ~ 54, 62 agilis (Ornithorhynchus) beat ne *albidus (Nyctonomus) 98 albipes (Conilurus) 114 albipes (Hapalotis) 114 »> (Sminthopsis) 10 *albocinereus (Mus) 108 Allied Rat 105 Alopecoid Carnivores 122 Ambergris 65 American Opossums dal EK Amphilestes Bec 8 anatinus (Ornithorhynchus) .. 2 annulus ‘xiv Anteater, Marsupial es oth 8 Anteaters .. i e xi., 61 Antechinomys ee not SiD anterior limb “epee tobe antibrachiwm SOC xiii. Antilopine Kangaroo ... 59 *antilopinus pean 59 Ape eee oes, Xs Apes ae eae xii., 61 apinalis (Conilurus) 116 : (Macropus) 57 ry (Phascologale) 14 apicalis (Potorous) 40 archeri (Pseudochirus) 29 Archer’s Opossum 29 Arctocephalus . 127 *argurus (Mus)... 110, 115 ariel (Petaurus) ... we 34 Armadillo ol Armadillos X., Xiil., 60 *aruensis pbpposiderus) . 85 assimilis (Mus) .. a .. 105 astralagus ooo xvi. atlas xis *aurantia (Rhinonycteris) 84 *aurata (Perameles) . ate PAGE Australian Long-eared Bat 87 7 Musk Rat ... 38 a Opossums ... 27 op Sea Bear 127 3 Sea Lion ... 126 Australian Water Rats ... 61 australis (Balena) 66 mages (Macroglossus) 81 3 (Miniopterus) . 95 i (Nyctonomus) . 98 3 (Petaurus) 33, 34 ae Wy (Taphozous) ... . 96 Pi ios (Vespertilio) .. 93 australis (Halicore) 64 » (Manatus) » xii. axis vas beg £4: wo. Xii. Aye-Aye ... aes a sem Ol Balena -. 66 Balenide... Xili., 66 Balenoptera . 68 Baleen 66 Baleen Whales 61 Banded Hare-Wallaby... 44 Bandicoot, Eastern Striped 21 3 Golden PP 23 a Long-nosed.. 22 33 North Australian . 22 3 Pig-footed .. 20 2) Short-nosed _ Jeon oo a Tasmanian Striped. 22 bs Western Striped ... 21 Bandicoots xili., 4, 7, 19, 20, 21 barbatus (Hrignathus) ... 129 Bat, Australian Long-eared ... 87 » Blackish-gray 91 », Brown Horseshoe 85 » Chocolate ... 90 » Dobson’s 90 » Hastern Forest 94, » Eawn-colored Horseshoe... 84 a), Gouldsshumess 91 » Great Blood-sucking 86 » Greater Horseshoe 30-88 » Great-footed uae «. 93 » Grey’s ade PED Poet » Krefft’s Be Pet sh) Oy luecho?s) 25 96 » Leche’s White Striped .. ive OS » (Petaurus) 132 INDEX PAGE PAGE Bat, Little ais 88 | breviceps (Phalanger) ... Tess » Little Fruit 81 | Bridled Wallaby MS aise wed » Norfolk Island 99 | Broad-faced Rat-Kangaroo ... 39 », Orange Horseshoe 84 | Broad-toothed Rat Aor ..- 120 » Pallas’ Fruit 81 | *brunneus (Pteropus) ... Owen’s 57 Horse-shoe Bat, Brown . 85 rf Plain Rat- .. 40 a Fawn-colored.. 84 Ss Queensland Tree- ... 44 oe Greater 83 PA Red ... re ace 38 s Orange 84. a Rufous-tailed Rat- ... 43 humerus : seoXtlle “a Tasmanian ... a5 Humpback ‘Whale 67 a Tasmanian Rat- 41 huttoni (Balenoptera)... 68 | Kangaroos 43 Hydromyine : ... 100 | Kerivoula 93 Hydromys si6%, 100, 102,103 | Killer... 73 Hyperoédon we 70, 71 | *kingi (Delphinapterus) 73 Hypsiprymnodon * ... 38] knee-cap ... xvi. Eesti unedbatine ise 38 | Kogia 70 Hyrax is Soo, bis || Mors Boe ix., 26 kreffti (Vesperugo) 89 ilium xv. | Krefft’s Bat cee 89 incisors pease us Jerboa-Rat 118 index seeXiVe - Pouched Mouse 14 Inia Bas . 64 imnominatum, os . .. xv. | Lagorchestes 45 inornata (Petrogale) . 49 | Lagostrophus 43 Insectivora : . 61 | lagotis (Peragale) “21, 24, 119 Insectivores .. x. | laniarius (Sarcophilus) . 18 insignis (Taphozous) 96, 97 | laniger (A ntechinomys) 9 interclavicle .- 1 | lanuginosus (Pseudochirus) 30 irma (Macropus) 51, 54 | lateralis (Petrogale) 49 Isabelline Kangaroo .. 58 | latifrons (Phascolomys) 25 *isabellinus (Macropus) 57, 58 | lawest (Echidna)... 3, 4 ischium ae F .. Xv. | layardi (Mesoplodon) ao, th *leadbeateri (Gymnobelideus)... 35 Jerboa Pouched Mouse... 9 | Leadbeater’s Opossum... 35 Jerboa-Rat, Black-tailed 117 | Leaf-nosed Bats... 82 - Bower’s ... 116 | Leche’s Bat ae 96 a Elsey’s LLG » White-striped Bat 98 - Fawn-colored .. 120 | leg. Ave x Krefft’s 118 leichhardti ‘(Lagorchestes) 46 on Long-haired 117 | Leichhardt’s Hare-Wallaby ... 46 5 Long-tailed 119 | lemuroides (Pseudochirus) 31 7 Mitchell’s... 119 | Lemurs... 61 FF Mouse-like 118 | Leopard, Sea... of . 129 a Nest-building 118 | *lepida (Dromicia) .. 36 % Peters’ . 115 | leporoides (Lagorchestes) 45 » 136 INDEX, PAGE PAGE leptonyx (Ogmorhinus) . 129 | maculata (Phascologale)... Sieh Lesser Brush-tailed Pouched maculatus (Dasyurus)... 17, 18 Mouse 56 soci 4 a ae 27, 62 Lesser Dormouse-Opossum 36 | magnum Bap abby » Flying Opossum .. 382 | *magnus (Macropus) 57 *lesueuri (Bettongia) ... 41, 42 | major (Macropus) weneg Lesueur’s Rat-Kangaroo 41 | Mammalia ob .. 104 leucas (Delphinapterus) 73 | Mammals, Eutheri ian 60, 61 leucogaster ee 5s} 53 Metatherian ... 4, 60 leucogaster (Hydromys) .. ao JKGHT ay Prototherian... oe *leucopus (Mus) ... 111 | Man ; xii., xiii. % (Sminthopsis) — » LL | Manatee ... : B50 Sat leucura (Echinothriz) ... 121 | Manatees ... ar noc 61, 68 *leucura (Peragale) .. 23| Manatus ... j .. 62 leucurus (Echiothria) ... 121 | manicatus (Mus) 105 limb, anterior ..xili. | Manide A Xs) kb » posterior “ae ... XV. | manus... i), OSL ove limbs i : oe: ... ix. | marginata (Neobalena) 67 lineolatus (Mus)... .. 105 | Marsupial Anteater... a8 Lion maa Oil tp Mole... ae 5, 115 Lion, Australian ‘Sea ... 126 | marsupial bones ... eee Xv., 4 Little Bat a 88 | Marsupialia ae 506 Ad: | rp, Leathe Bat... 81 | Marsupials... x., xil., xili., ee Xvi., » Pouched Mouse ne prea} ; 4 60 peat .. 108 | Marsupials, Mesozoic Potypete » Rock- Wallaby F su 48 dont . ; & *lobatus (7alcohiey, 125, 126, 127 | Mar. supiata 114 Long-eared Bat, Australian ... 87 | Marsupium Ee », haired Jerboa-Rat so tla) Massive-toothed Whale. val », haired Rat ... 106 | Mastacomys 120 »» nosed Bandicoot... 22 | medius xiv. », snouted Pouched Mouse.. 37 | Meduse 65 » tailed Jerboa-Rat alg Megachiroptera... 77 toothed Whale ... ... 71 | Megaderma 85 Long- -tailed Pangolin Fgh als Mesadermine : 85 longicaudata (Manis) Pej peli megaphyllus (Rhinclophus) 83 longicaudatus (Conilurus) —... 119 ; Megaptera di 67 longipilis (Mus) ... 106 | melanops (Macropus) . 60 lumbar vertebre .. ... xii. | melas (Globicephalus)... 74 lumholtzi (Dendrolagus) 44 | meso-cuneiform bone sive lunata Sega hed 47 | Mesoplodon Ses ye Per is lunar bone A xiv. | mesosternum er xiii Lupine Carnivores 122 | metacarpus 5) EE 1G Lee Lycaon ... : 122 | metatarsus . Xvi. lyra (Megaderma) 86 | Metatheria 4, 114 Mice ae Mn Mes: . 103 macrocephalus Ce tae 69 | Mice Pouched : 2?! ... oem Macroglossi 80 | Microchiroptera : 82 Macroglossus 81 | microdon (Chalinolobus) 90 ‘Macropodide xii, 88 | microtis (Nyctophilus) . 88 Macropodine 43 | *minima ears el aos Macropus : 51 | minimus ... 585 500 Xiv. macropus (Uromys) 121 | Miniopterus 94 Macrorhinus : 128 | minor (Petauroides) .. ia oe *macrura (Perameles) ... 22 | minutissima (Phascologale) 12, 18 *macrurus (Conilurus)... 115 | mitchelli (Conilurus) ... fel) macrurus (Sminthopsis) ... vie LO rf (Phascolomys) ia 25 INDEX 137 PAGE PAGE Mitchell’s Jerboa-Rat ... 119 | Narwhal . A x., 61 Molars ... ete .. xX, | nasuta (Perameles) 21, 22 Mole, Marsupial _ 5, 115 | Native Bear Fee 26 » South African Golden ise LD » Cat, Black- tailed 15 a Water -f'... 51 DOD ei % Cat, Common ... 16 Mole te wee th fd ERS 3 Cat, North- Australian... 15 Moles ais 61 » Cat, Slender... Bena d Wy Molossinz 97 rs Cat, Spotted-tailed 17 Monachus... 125 a Cats a scot PH LOD LS Monkeys ... ix.,61 op DYoy 123 Monodelphia i Porcupine Sue AOL Monotremata Native Rabbit 114 Monotremes TBs | XV.» 6, ", to navicular bone ... xvi. morio (Chalinolobus) . he Nest-building J erboa-Rat 118 moschatus (Hypsiprymnodon) 5 38 New Zealand. Dolphin ... soon 10) Mouse, Common Field... ... 109 | nigrogriseus (Chalinolobus) ... 91 » Common Pouched 10 | *norfolcensis (Nyctonomus) 99 » Freckled Pouched 14 | Norfolk Island Bat see 99 » Grayish-white .. ... 108 | North-Australian Bandicoot . 22 » Greater Brush-tailed Pouched cane de » Jerboa Pouched natant’) o Krefft’s Pouched 14 55 Lesser Brush-tailed Pouched : sete lee » Little Pouched.. 13 » Long-snouted Pouched 37 35 Pigmy ... uae . 109 Hf Pigmy Pouched 12 », Striped-faced Pouched.. 11 r Swainson’s Pouched ... 14 » Thick-tailed Pouched... 10 » White-bellied Pouched.. 13 » White-footed Pouched., 11 » Wooly Pouched 9 Yellow-footed Pouched 13 Mouse-like Jerboa-Rat.. sce wilfs! Muride do 100, 102 murina (Sminthopsis) sie LO Murine ... .. 103 murinus (Conilurus) 4 NSS murinus (Potorous) 40 Mus 102,103,110,112, 113, 114, 120, 121 musculus (Mus) . 103, 109 Musk-Ox ... be cee Musk Rat, ‘Australian . 38 Mustelide.. : 15 Myogale ... : vs Sao EX: *myoides (Xer omys) .. 102 Myrmecobius 4 2 8, Myrmecobiine ... “as Myrmecophagide... oa a Mystacoceti "64, 65 Nail-tailed Wallaby 48 nana (Dromicia) 36 *nanus (Mus) ... . 108 Native Cat... 15 notatus (Petawrus) on see) eee Notoryctes add oe 6, 7, 115 Notoryctidee é ies es *nove-hollandize (Mus) 109 nove-zealandize (Delphinus) ... 75 nove-zealandic (Megaptera) 68 Nycteride aoe 85 Nyctonomus 97 Nyctophilus Bee Ou obesula (Perameles) ... 21, 23 obturator foramen SESLEA YS *occidentalis (Pseudochirus) noce waX0) ocydromus (Macropus) . 59 ogilbyi (Bettongia) 43 Ogmorhinus 129 Onychogale 47 Oota ‘ wae 2400 opisthocelous vertebra ae gee Xde Opossum, Archer’s 29 ay Common . 28 } Common Dormouse.. 36 Hs Common Ring- tailed 30 ¥ Greater Flying Lay ll es Herbert River 30 ES Leadbeater’s 35 > Lesser Flying 32 5 Lesser Dormouse 36 fe Pigmy Flying 36 Le Short-eared .. 28 A Squirrel-like Flying 34 PA Sombre F 31 55 Striped 32 33 Tasmanian .., 28 Fs Tasmanian Ring-tailed 29 3 Western Ringtailed.. 30 a Western Dormouse... 35 a Yellow-bellied Flying 33 138 INDEX. PAGE PAGE Opossums, Australian ... 27 | Phyllorrhina eke 83, 84 Opossums ... ine nD ix., x. | Physeter ... 3 Oo 5 American : ... 1x. | Physeteride 69 UE HD. “cane nC .. 4] Physeterine ... 69 Orange Horseshoe Bat... .. 84] picatus (Scotophilus) . 91 Orca "a6 65, 73 | Pied Bat... 91 orientalis (Phalanger) oer .. 4] Pigmy Flying Opossum 36 Ornithodelphia ia’ 1, 60 » Mouse 109 Ornithorhynchide ae Jae pate. », Pouched- Mouse... 12 Ornithorhynchus ee SOROS » Right Whale ; 67 os innominatum .. 3 xv. | Pig-footed Bandicoot ... ee) Otariide ... res 126, ae Pilot Whale «ea owent (Echidna) ... : Pinnipedia 60, 125 Owen’s Kangaroo 57 pisiform bone . Xiv. Placentalia 60 *pachyurus (Mus) 112 | Plain-colored Rock- Wallaby . 49 Pademelon : 52 | Plain Rat a | 105 Pallas’ Fruit Bat. 81 » kat- Kangaroo 40 Pangolin, Long-tailed xii. | *planifrons (yperrgan) 71 EIS OTE : ou X., Xl. | plantigrade ie xv *papuensis ( (Kerivoula) 94 | Platanista 69 Papwuina 17 | platyops (Potorous) 39 parma (Macropus) 52 | Platypus ... seagligpe parryi (Macropus) 55 | Platypus, Duck-billed .. ate? ee Parry’s Wty .. 55] Plecotus nip ‘eee, patella .. Xvi. | Plicated Bat 98 pelvis aise .. Xv. | *plicatus (Nyctonomus) 98 peaiailata (Bettongia)... 42, 43 | Podabrus ... 10 es (Petrogale)... . 50] poliocephalus (Pteropus) 78 a (Phascologale) . 12 | pollex mae xiv. penicillatus (Conilurus) 117 Polyprotodontia.... : . 4,6 Peragale ... 23 | Porcupine, Native a0 oo 8! Perameles 20 | Porcupines 61 Peramelidee : xlil., a "7, 19 | Porpoises ... 65 peregrinus (Pseudochirus) 30 | posterior limb 5 2% Pericheta . se 17 | Potoroine 39 personatus ‘(Conilurus) 118 | Potorous.. 5 39 pes.. xv. | Pouched- Mouse, Common 10 Petaurista... 31 Fe Freckled 14 Petauroides Aor 24, 31 i Greater Brush- Petaurus . . 24, 38, 34 tailed 12 Peters’ Bat 0, eae 09: Pe Jerboa pee) », Jerboa- Rat . 115 38 Krefft’s 14 *petersi (Nyctonomius)... 99 35 Lesser Brush- Petrogale... .. 48 tailed 12 Phalanger 4, 24, 27 is Little... 13 Phalangerids 25 a Long-snouted. 37 Phalangerine ... aes 27 x Pigmy os SLD, phalanges ... sh epee exvile 35 Striped-faced.. 11 phalangigrade ae XV. x Swainson’s ... 14 Phascolarctine ... 26 x Thick-tailed... 10 Phascolarctus Bone 240) e White-bellied. 13 Phascologale it 4, 6,11 Fs White-footed.. 11 Phascolomyide ... sal 824: ae Wooly a! Phascolomys a an Pa a Yellow-footed.. 13 Phascolotherium ... ee ... 8] Pouched Mice ... : a wee Phocide ... 128 | premolars ... Sa nee ban, ao INDEX. 139 PAGE PAGE presternum xiii. | Rat, White-footed 105 primevus (Cyon)... 123 | ,, White-tailed 110 Primates ... ae Acc 61 | Rat-Kangaroo, Broad-faced ... 39 Proechidna oes AOC eae iL os Brush-tailed ... 42 Prototheria funy Ix G RS Common 40 Prototherian Mammals ... as a Gaimard’s 42 Pseudochirus 24, 29 ie Gilbert’s 39 Pseudorca ye 18 P Lesueur’s 41 Pteromys ... 31 i Plain .. 40 Pteropodide 77 ae Rufous 43 Pteropine Bats 78 on Tasmanian 41 Pteropus.. 77 | Rat-Kangaroos ... shes Hoe pubis wes xv. | Rats ed Shc 61, 103 pumilus (Vesperugo) os 88 | Rats, Australian Water .. ail pygmeus (Acrobates) ... 36 | Red Kangaroo ... 58 Red-legged Wallaby 53 Quadrangular-tailed Rat ... 118 | Red-necked Wallaby .. noo Quadrumana ‘ Hol 3 Wallaby, Tasmanian 56 Queensland Serub- Wallaby 57 | Rein-Deer... ie aor oe Gl on Tree-Kangaroo 44 | Reptigrada ; 128 Rhinoceroses ae aes sao) BSS Rabbit-Bandicoot,Common ... 24} Rhinolophide 82 ne White-tailed 23 | Rhinolophine 82 Rabbit, Native ee . 114 | Rhinolophus 82 Rabbits ; 61 | Rhinonycteris 83 radial sesamoid bones ..Xiv. | Rhododendron 17 vadws ... oe ... Xlil. | Rhytina 62 ramsayt (Behidna) See ... 3] Ribs, false... xiil. Rat sy ae Vili.| ,, floating xiii. Rat, Allied ae 105 | ,, sternal Xili. » Australian Musk . 38 Bue Liteenen. ee Xili. » Blue ets 110 | Right Whale, Pigmy fit 67 ss Broad-toothed 120 a Southern 66 » Bufi-footed 121 | Ringed Seal 55 lr48) » Burton’s 107 | Ring-tailed Opossum, Common.. 30 », Chestnut- colored .. 112 93 Opossum, Tasmanian 29 » Dusky-footed 104 Opossum, Western.. 30 » Hastern Water 101 | robustus (Macropus) 58 5 Giant 121 | Rock-Rabbit * Lexis aa OULAIS) |. os 107 | Rock-Wallaby, Brush- tailed . 50 - Gray’ s White-footed 107 33 Little ... 48 » Grey’s 108 wa Plain-colored... 49 » Little 108 - Short-eared 49 » Long-haired 106 in West Australian 49 » Plain 105 An Yellow-footed.. 50 Es Quadrangular-tailed 113 | Rodentia .. 61, 99, 100, 104 » Short-tailed 111 | Rodents ... ee Exe »» Simson’s 111 | rostrata (Balenopter a) . bc Back? (ste! » Sordid 106 | rostratus (Tarsipes) . 37 » Swan’s AS 111 | rueppelli (Scotophilus) | 92 » Tasmanian Water 112 | rufescens (Eipyprymnuus) 43 » Tawny 104 | ruficollis (Macropus) 56 »» Thick- tailed 112 * var. bennetti (Macropus) 56 3 ‘chomas’ 102 | Rufous-bellied Wallaby 51 », ‘Tlompson’s ... 109 53 Hare-Wallaby ... 45 » Velvet-furred 106 » Rat Kangaroo... 43 » Western Water 102 | rufus (Macropus) 58 140 INDEX. PAGE PAGE rufus (Dendrolagus) ... ... 45} Sombre Opossum as So! 3, (Potorous)... she 40 | Sordid Rat ae con +» 106 Ruminants 8 at ... x. | sordidus (Mus) ... As 106 Riippell’s Bat 92 | Soricide ... “68 Ser “os EWe Sotalia AK set Ge sacral vertebre xii. | Southern Bottlenose ... GT sacrum XV. ye Bottlenose Whale ... 71 Sarcophiius 18 5 Right Whale 66 scaphoid done xiv. e (White?) Whale ... 73 scapula... oe xii. | Spectacled Flying-Fox «se 80 scapulatus (Pteropus) xt 80 93 Hare Wallaby ... 46 Schreibers’ Bat . sed 94 | speleus (Thylacinus) . Ag *schreibersi, (Miniopterus) 94, 95 | Sperm Whale ... s08 «s« (69 sciureus (Petaurus) 34 a Short-headed ... 70 Scotophilus aie ne ... 91 | Sperm Whales ae » 65 Serub Wallaby ... 56 | Spotted Cuscus . bes em is yy Common . 57 | Spotted-tailed Native Cat veil 55 Queensland ... 57 | Squirrel-like Flying- gayi 34 Sea Bear, Australian ... 127 | Squirrels, Flying... 56 re » Hlephants .. 128 | Stenorhynchus .,.. 129 » Leopard ... 129 | sternal ribs sis ee xiii, + Lion 5 mee ... 126 | sternum ... Ps xi. Seal Ae 61 | stigmaticus (Macropus) . 53 Seals TS Ayr, GO! 65, 125 Striped- faced Pouched Mouse... 11 » Hared . 126 eA Opossum wae Ree a » Harless . 128 | structures, tegumentary ... ix. Seal, Bearded .. 129 | subplantigrade ... aes ‘ee We » Ringed ... 129 | Sulphur-bottom ... 68 sesamoid bones ...Xiv. | swainsoni (Phascologale) 14 setosa (Hchidna) ... .. 3, 4| Swainson’s Pouched Mouse 14 Sharp-nosed Bat ... 96] Swan’s Rat 111 Sheep ae gag ... OL | Swine . Ne 61 Short-eared Opossum ssi 28 | system, dental ... cia teal » eared Rock-Wallaby ... 49 » headed Sperm Whale ... 70 | tabernaculi (Halicore) 63 », nosed Bandicoot .. .. 2 | taal ies ah are Leis » tailed Rat.. Ms .. 111 | Talpide xv. tailed Wallaby ... 51 | *tamarensis (Mus) 112, 113 shoulder- -girdle sé ... xiii. | Taphozous 95, 97 Shrews 61 | Tapir 61 *sionifer (Chalinolobus) ... 90) Tarsipedins 37 simsoni (Mus) «os LD | Barsipes :.. 26, 37 Simson’s Rat sis ... L11 | tarsus xwle Sirenia xvi., 60, 61, 62 | Tasmanian Devil 18, 125 Sirenians ... xv., 62 oh Kangaroo ... Batt skeleton ... les wae Bee tipo, 33 Opossum 28 BS appendicular . soos atk. or Rat-Kangaroo 41 skull be eas ¥: Red-necked Wallaby 56 Slender Native Cat ile es Ring-tailed Opossum 29 Sloths 5 .. 60 ee Striped Bandicoot.. 22 Sloth, Three- £060. epexalits > Water Rat... .. 112 >» Lwo-toed . peexell ss Wolf 19 Small-footed Bat 93 = Wombat ee 15) >» toothed Bat a 90 | Tawny Rat ute ... LO4 », toothed Whale ... 72 | tegumentary structures ... Feet Lie Sminthopsis oes ee Se 9 Sminthus .,. oS .. LOO i agyen 493 terre-reginz (Mus) *tetragonurus (Mus) INDEX. 141 PAGE PAGE thetidis (Macropus) ... 52] Wallaby, Branded 53 Thick-tailed Pouched Mouse... 10 ry. Bridled 3: wien AT Rat 4 uf ly? re Brush-tailed Rock- oeto) thigh see : Be Ayo iS Cape York i be Thomas’ Rat . 102 i, Common Hare- 45 Thooid Carnivores 122, 123 ¥ Common Serub 57 thoracic vertebre .. 4 pally P Crescent 47 thorbeckiana (Phascologaie) 15 oF Grey’s =e. OO Three-toed Sloth . Agar - Leichhardt’s “Hare-... 46 Thylacine ae 7 a Little Rock-.. .. 48 Thylacinus Key ee ie 18, 19 5 Nail-tailed 48 Thylacoleo . 124 39 Parry’s ae KOO tibia e Sek abo Bae > Plain-colored Rock-.. 49 Tiger, Marsupial... > » Queensland Scrub ... 57 timoriensis (Nyctophilus) 87 Red-legged ... 53 titan (Macropus)... Wee 125 D Red-necked ... 56 *tompsoni (Mus) 109 9 Rufous-bellied 51 Tompson’s Rat ... 109 5 Rufous Hare- 45 Tortoises ... ore x. a Scrub.. 56 trapezium .. Xiv. _ Seont-caccd Bock- \. 49 trapezoid . Xiv. oS Short-tailed . 51 Tree-Kangaroo, Queensland w. 44 Py Spectacled Hare- 4.6 Trichosurus : F 24, 27 39 Tasmanian Red-necked 56 tridactylus (Potorous)... . 40 25 WestAustralian Rock- 49 tridactylus (Bradypus) . be 2k 5s White-throated 52 trivirgata (Dactylopsila) 32, 62 Yellow-footed Rock... 50 True Opossums ie 4 Wallaroo .. sou ie: tuberculatus (Chalinolobus) . 90) Walrus 61 Tula . aad 29 | Walruses... ‘60, 125, 126 Tursio 76 | Warrigal 123, 124, = Tursiops ... 76 | Water-Mole ac dc Two-toed Sloth Bs xii. | Water Rat, Eastern ae typhlops (Notoryctes) .. 5 Sar at. % Tasmanian . 112 vs Western .. .. 102 ulna oo x1 Wate nate Australian.. 61 ulna sesamoid bones Xiv.| Weasel ... 61 unciform bone XIV. | West Australian Rock ‘Wallaby 49 ungual phalanges... XlV. | Western Dormouse Opossum... 35 Ungulata... x1., 61 x Ring-tailed Opossum.. 30 Ungulates... xil. » Striped Bandicoot ... 21 unguligrade “ Xv. Water Rat 102 unicolor (Nyctophilus 87 Whale, Ca’ing ... 74, Uromys ... 121 » Hump-back 67 Uronycteris 80 » Long-toothed ... 71 *variabilis (Mus) ay ee Lenco atl ad 71 vellerosus (Mus)... 104 » Pigmy Right . 67 *velutinus (Mus) 106} » Hea eee va virgini = - 55 mall-toothe pretnae, (Sunintbopels) ae Fy Southern Bottlenose seas *walkeri Sea tome wa 87 » Southern Right 66 Walker’s Bat... es 87 Southern ee ?) 73 Wallabies ves 43 Whale-bone ae 65, 66 Wallaby, Agile .. fo 54 33 Whales xili., 65 7 Banded Hare- 44.| Whales ix., xlii., xv., 60, 65 Bs Black-gloved 54 » Baleen re Terk a Black-striped 55 » Sperm 61, 65 s Black-tailed ... 57 » Whalebone Xlil., 65 142 INDEX. PAGE PAGE White Bear See ... 61! Wombat, Common Australian... 25 White-bellied Pouched Mousee 13 nA Hairy-nosed .. 25 » footed Pouched Mouse... 11 Tasmanian sop » tooted Rat a 105 Woolly Pouched-Mouse iArng, » footed Rat, Gray’s so MG7/ » footed Jerboa-Rat - 114 | xanthopus (Petrogale) ... -. BO » striped Bat BY 98 Xeromys 102 », striped Bat, Leche’s 98 wiphisternum, ati » tailed Rabbit-Bandicoot 23 Lage i », tailed Rat Aa jos HINO) » throated Wallaby a 52||. X@p-pl %.. ooo . dl tipped Jerboa- Rat 116 Yellow- bellied Bat Sane 96 ileoxi (Macropus) 53 », bellied Flying-Opossum 33 williamsoni (Arctocephalus) . 127 » bellied Rock-Wallaby... 50 Wolf ae 61, 122 » footed Pouched Mouse.. 13 » Marsupial ... abc sia oXs » headed Bat . 89 Wolf, Tasmanian Bob we 19 Wolves... Ses a6 ... xX. | Zalophus... ... 126 Wombat ... aoe dc ... ix. | Zeuglodons 65 Wombats... 24} Ziphiine .. 70 : F, W. WHITE, PRINTER, | MARKET STREET, SYDNEY. PUBLICATIONS OF THE AUSTRALIAN MUSEUM. DECEMBER, 1892. I.—CATALOGUES. CATALOGUE OF THE SvEcIMENS OF NaTurAL History AND MISCELLANEOUS CURIOSITIES IN THE AUSTRALIAN Museum, by G. Bennett. 1837. 8vo. pp. 71. (Out of print.) CATALOGUE OF Mamaia IN THE COLLECTION oF THE AUSTRALIAN Musevuy, by G. Krefft. 1864. 12mo. pp. 133. (Out of print.) ‘CATALOGUE OF THE MINERALS AND Rocks IN THE COLLECTION OF THE AUSTRALIAN _ Muszum, by G. Krefft. 1873. 8vo. pp. xvii-115. (Out of print.) CATALOGUE OF THE AUSTRALIAN BirDS IN THE AUSTRALIAN MoseEvm, by E. P. Ramsay. Part I. Accipitres. 1876. 8vo. pp. viii-64. Boards, 2s.; cloth, 3s. Part II. Striges. 1890. 8vo. pp. 35. Wrapper, 1s. 6d. Part III. Psittaci. 1891. 8vo. pp. vili.-110. Wrapper, 5s. CATALOGUE OF THE AUSTRALIAN STALK AND SEsSILE-EYED CrusTacga, by W. A. Haswell. 1882. 8vo. pp. xxiv.-324, with 4 plates. (Scarce) Wrapper, 21s. CATALOGUE OF THE LIBRARY OF THE AUSTRALIAN Museum. 1883. 8vo. pp. 178. Wrapper, ls. 6d., with two supplements. (Out of print.) CaTaLogun or A CoLLECTION or FossILs IN THE AUSTRALIAN Museum, witH INTRODUC- Tory Norss, by F. Ratte. 1883. 8vo. pp. xxviii-160. Wrapper, 2s. 6d. CATALOGUE OF THE AUSTRALIAN Hyproip ZoopHyTEs, by W. M. Bale. 1884. 8vo pp. 198, with 19 plates. Wrapper, 3s. 6d. ; - Descriprive CATALOGUE OF THE GENERAL COLLECTION OF MinERALS IN THE AUSTRALIAN Museum, by F. Ratte. 1885. 8vo. pp. 221, with a plate. Boards, 2s.6d.; cloth, 3s.6d. 2nd Edit., 1890. _ Descriptive CATALOGUE OF THE MEDUS# OF .HE Austratian Sas. Part I. Scypho- meduse. Part II. Hydromeduse, by R. von Bendenfeld. 1887. 8vo. pp. 32 and 49, (Withdrawn from sale.) Descriptive CATALOGUE OF THE Nests AND Eaas OF AUSTRALIAN Birps, by A. J. North. 1889. 8vo. pp. iv. v.-407, with 21 plates. Wrapper, 12s. 6d. Coloured plates, £2 5s. Descriptive CATALOGUE OF THE SPONGES IN THE AUSTRALIAN Muszum, by R. von Lendenfeld, 1888. 8vo. pp. xiv.—260, with 12 plates. Boards, 7s. 6d.; cloth, 10s. 6d. CATALOGUE OF THE FisuEs IN THE AUSTRALIAN Museum. Part I. Paleichthyan Fishes, by J. Douglas Ogilby. 1888. 8vo. pp. 34. Wrapper, 2s. 6d.; boards, 3s. 6d. CATALOGUE OF THE Marine Snetis or AUSTRALIA AND TasmaniA, by J. Brazier. Part I. Cephalopoda, 1892. 8vo. pp. 20. Paper, 2s. 6d. Part Il. Pteropoda, 1892. 8vo. pp. 22. Paper, 2s. 6d. , CATALOGUE OF AUSTRALIAN Mamma .s, with Introductory Notes on General Mammalogy, by J. D. O gilby, 1892. 8vo. pp. xvi.-144. Wrapper, 3s. 6d. IIl.—_MOGNOGRAPHS. _ AusTRALIAN LEPIDOPTERA AND THEIR TRANSFORMATIONS, by the late A. W. Scott, with Illustrations by his daughters, Mrs. Morgan and Mrs. Forde. Edited and revised by A. §, Olliff and Mrs. Forde. Vol.II., Parts],2 & 3. Wrappers, 15s. each. TII.—MEMOIRS. . History AND DESCRIPTION OF THE SKELETON OF A NEW SPERM WHALE IN THE Ausrrauian Museum, by W. S. Wall. 1851. 8vo. pp. 66, with plates. Reprint 1887. Wrappers, 2s. 6d. . Lorp Howse Istanp, rvs ZooLoey, GroLogy, AND PuysIcaL CHARACTERS. 1889. 8yo. Pp: viii.-132 with 10 plates. Boards, 7s. 6d.; cloth, 10s. 6d | | 5 Publications of the Australian Museum.—Conrivzp. IV.—GUIDES. 1 GurpE TO THE AUSTRALIAN FossiLn REMAINS IN THE AUSTRALIAN Museum. 1870. (Out of print.) 2. GUIDE TO THE CONTENTS OF THE AUSTRALIAN Musrum. ‘1883. 8vo. pp. iv.t Wrapper, 3d. (Out of print.) 3. GUIDE TO THE CONTENTS OF THE AUSTRALIAN Musreum. 1890. 8vo. pp. Wrapper. V.—MISCELLANEOUS PUBLICATIONS. 1. List or Otp Documents AND RELICS IN THE AUSTRALIAN Musrum. 1884, Reprin' with additions, 1890. 8vo. pp. 4. 2. DescripTIvE List oF ABORIGINAL WEAPONS IMPLEMENTS &C., FROM THE DARLING Lacuian Rivers, by K. H. Bennett, F.L.S. 1887. 8vo. pp. 8. (Out of print.) . ~ 8. Notrs For CoLLecTors. 1887. S8vo. 1s. 4. HINTS FOR THE COLLECTORS OF GEOLOGICAL AND MINERALOGICAL SPECIMENS, by F. Ratt pp. 26, with a plate. 6d. » 5. Hints FoR THE PRESERVATION OF SPECIMENS Of NATURAL History, by E. P. Ramsa| 1891. 4th Edition. pp. 32. Is. VI.—RECORDS. Vol. I., March, 1890 to Decr. 1891. 8vo. pp. 202. 30 plates. Boards. Price 25s. Vol. II., No. 1. April, 1892. 8vo. pp. 22. 3 plates. “Wrappers. Price, 2s. 6d. » No. 2. -August, ,, 53 fc eP Pols. Aces, is 4 ) 2s. 6d. yo INO: ca-eeSte, os oD Dal Orie