PROCEEDINGS OF THE BIOLOGICAL SOCIETY OF WASHINGTON 116(3):699-709. 2003. Chromosomes of Philippine mammals (Insectivora, Dermoptera, Primates, Rodentia, Carnivora) Eric A. Rickart Utah Museum of Natural History, 1390 E Presidents Circle, University of Utah, Salt Lake City, Utah 84112, email: [email protected] — Abstract. Karyotypes of nine species of Philippine mammals representing five orders are presented. Chromosomes of six species are described for the first time, including three endemic insectivores (Podogymnura truei, Crocidura beatus, C. grayi), the endemic dermopteran {Cynocephalus volans), an endemic squirrel {Sundasciurus philippinensis), and a widespread viverrid {Viverra tan- galunga). Some species endemic to the oceanic Philippines have unique kar- yotypes whereas other endemics and widespread Asian species have karyotypes that are similar, or identical, to those ofrelated species or conspecifics occurring outside the archipelago. These data corroborate patterns of karyotype variation previously documented for Philippine bats and murid rodents. For more than a century, the terrestrial land), and 1993 (Mindanao Island). Live- mammal fauna of the Philippines has been trapped animals were processed and killed recognized as a unique assemblage (Thom- with sodium pentobarbital within 24 h of as 1898). All portions of this remarkable capture, and karyotypes prepared from fauna, which includes 179 species repre- bone marrow and/or spleen cells following senting nine orders, are characterized by a in vivo methodology (Patton 1967, Rickart high proportion of endemic species. More et al. 1989). Material from freshly killed an- than 60% of the mammal fauna, as a whole, imals caught in snap traps was processed in is endemic (Heaney et al. 1998). For bats vitro (Rickart et al. 1998). Cells were pro- and murid rodents, the two largest faunal cessed and fixed in the field, and standard components, cytogenetic studies have pro- (non-differentially stained) karyotypes were vided insight into how these groups have prepared from stored cell suspensions. diversified within the archipelago (Rickart Preparations of silver-stained nucleolus or- et al. 1989, Rickart & Musser 1993, Rickart ganizer regions (Ag-NORs; Howell & & et al. 1999, Rickart Heaney 2002). These Black 1980) and G-banded chromosomes studies suggest that chromosomal data on (Seabright 1971) were made for some taxa. other Philippine taxa may help clarify their A minimum of 10 chromosomal spreads phylogenetic and biogeographic relation- was examined from each preparation. Chro- ships. Accordingly, this report presents kar- mosome terminology follows Rickart and yotypes of nine species representing five or- Musser (1993). As used herein, fundamen- ders (Insectivora, Dermoptera, Primates, tal number (FN) refers to the total number Rodentia, and Carnivora). of chromosome arms in the female karyo- type (including those of sex chromosomes). Methods Species nomenclature follows Heaney et al. (1998). Specimens were collected during field Voucher specimens were prepared as studies conducted in 1987 (on Leyte, Bili- skins with partial skeletons, complete skel- ran and Negros islands), 1988 (Luzon Is- etons, or preserved in fluid, and are depos- —— 700 PROCEEDINGS OF THE BIOLOGICAL SOCIETY OF WASHINGTON ited in the Field Museum of Natural His- 459818); Mount Pangasugan, 8.5 km N, 2.5 tory, Chicago, IL (FMNH), the National km E Baybay, elev. 500 m, 10°45'30"N, Museum of Natural History, Smithsonian 124°49'30"E, 1 male (USNM 458723). Institution, Washington, DC (USNM), and Sundasciurus philippinensis (Water- — the Philippine National Museum, Manila house, 1839). Biliran Island, Leyte Prov- (PNM). Microscope slides of chromosomal ince, 5 km N, 10 km E Naval, elev. 850 m, preparations and photomicrograph nega- 11°36'N, 124°29'E, 1 male (USNM tives cross-referenced to cataloged voucher 459821). specimens are housed at the Utah Museum Paradoxurus hermaphroditus (Pallas, — of Natural History, University of Utah, Salt Mil). Leyte Island, Leyte Province, 7 km Lake City. N, 1.5 km E Baybay, elev. 50 m, 10°45'N, 124°48'E, 1 male (USNM 458891); Mount Specimens Examined Pangasugan, 10 km N, 2 km E Baybay, elev. 300 m, 10°46'N, 124°49'E, 1 male Podogymnura truei Mearns, 1905. (USNM 459999). — Mindanao Island, Bukidnon Province, Viverra tangalunga Gray, 1832. Leyte Mount Kitanglad Range, 16.5 km S, 4 km Island, Leyte Province, Mount Pangasugan, E Camp Phillips, elev. 1900 m, 8°10'30"N, 10 km N, 2 km E Baybay, elev. 300 m, 124°5rE, 2 males (FMNH 147793, 10°46'N, 124°49'E, 1 male (USNM 147798). 460000). — Crocidura beatus Miller, 1910. Leyte Island, Leyte Province, Mount Pangasugan, Results 10 km N, 4.5 km E Baybay, elev. 950 m, 10°47'N, 124°50'E, male (USNM Order Insectivora 1 Family Erinaceidae 457984). — Crocidura grayi Dobson, 1890. Luzon Podogymnura truei. 2N = 40, FN = 76, — Island, Camarines Sur Province, Mount Is- Fig. lA. The karyotype of the Mindanao arog, 4 km N, 22 km E Naga, elev. 1750 gymnure includes 1 1 pairs of small to large- m, 13°40'N, 123°22'E, 1 female, 1 male sized metacentric or submetacentric auto- (USNM 573607, 573617). — somes, 6 pairs of medium-sized subtelocen- Suncus murinus (Linnaeus, 1766). Ne- tric autosomes, and 2 pairs of small or me- gros Island, Negros Oriental Province, Sil- dium-sized telocentric autosomes. The liman Farm, Dumaguete, elev. 5 m, small X chromosome is submetacentric, (USNM 09°18'N, 123°18'E, 2 males and the minute Y chromosome appears to 457996, 457997); Mount Guinsayawan, 3 W be telocentric. km N, 17 km Dumaguete, elev. 1470 m, 9°22'N, 123°9'E, 1 female, 1 male (USNM Family Soricidae 458970, 458972). Cynocephalus volans (Linnaeus, Crocidura grayi. 2N = 38, FN = 58, Fig. — — 1758). Leyte Island, Leyte Province, 7 km IB. The karyotype of the Luzon shrew in- N Baybay, elev. 10 m, 10°45'N, cludes 4 pairs of small to medium-sized 124°47'30"E, 1 female (USNM 458982). submetacentric autosomes, 5 pairs of small Tarsius syrichta (Linnaeus, 1758). to large-sized subtelocentric autosomes, and Leyte Island, Leyte Province, 7 km N, 1.5 9 pairs of small to large-sized telocentric km E Baybay, elev. 50 m, 10°45'N, autosomes. The X chromosome is medium- 124°48'E, 1 male (PNM specimen, EAR sized and subtelocentric, and the small Y field number 1441); Mount Pangasugan, chromosome is submetacentric. 10.2 km N, 2.2 km E Baybay, elev. 320 m, Crocidura—beatus. 2N = 38(?), FN = ?, 10°46'N, 124°49'E, 1 male (USNM not figured. A poor quality in-vivo prep- VOLUME NUMBER 116, 3 701 A M KK jm %n XX ^j( »l «ft ^'ift^* lift ftft AA • - ? Y B XA XX XX ^A Kl^ on 0^ Ao 06 />o no aa Aa AA KM*''*-- )[y A«A« VV f(» Ali ft* Ao AO 9(\ An iio All Fig. 1. Karyotypes of: A) Podogymnura truei, male (FMNH 147793) from in vitro preparation, 2N = 40; B) Crocidura grayi, male (USNM 573617), 2N = 38; C) Suncus murinus, female (USNM 458970), 2N = 40. 702 PROCEEDINGS OF THE BIOLOGICAL SOCIETY OF WASHINGTON aration yielded preliminary information on Island includes 9 pairs of metacentric or the chromosomes of this species which is submetacentric autosomes, 7 pairs of sub- endemic to the Mindanao faunal region. telocentric autosomes, and 2 pairs of small The modal chromosome count from multi- telocentric autosomes. The medium-sized X ple spreads was 38, indicating a karyotype chromosome is submetacentric and the mi- similar to that of C grayi (Fig. IB). nute Y chromosome appears to be telocen- Suncus murinus. 2N = 40, FN = 60, Fig. tric. — IC. Specimens of the Asian house shrew from Negros Island have a karyotype that Order Carnivora includes 4 pairs of small to large-sized sub- Family Viverridae metacentric autosomes, 5 pairs of small to Paradoxurus hermaphroditus. 2N = 42, medium-sized subtelocentric autosomes, — FN = 72, Fig. 4A. Specimens of the com- and 10 pairs of medium to large-sized telo- X Y mon palm civet from Leyte Island have a centric autosomes. Both the and chro- karyotype that includes 8 pairs of small to mosomes are submetacentric. large-sized metacentric or submetacentric autosomes, 6 pairs of small to large-sized Order Dermoptera subtelocentric autosomes, and 6 pairs of Family Cynocephalidae small to medium-sized telocentric auto- Cynocephalus volans. 2N = 38, FN = somes. The medium-sized X chromosome — Y 40, Fig. 2. The standard karyotype of a is submetacentric, and the small chro- mosome female Philippine flying lemur from Leyte is telocentric. Island includes 18 pairs of small to large- Viverr—a tangalunga. 2N = 36, FN = 64, sized telocentric autosomes and a pair of Fig. 4B. The karyotype of a male Malay medium-sized submetacentric X chromo- civet from Leyte Island includes 7 pairs of somes. A G-banded preparation reveals G- small to large-sized metacentric or sub- positive bands on the nine largest auto- metacentric autosomes, 6 pairs of small to somes. The X chromosome is largely G- large-sized subtelocentric autosomes, and 4 positive. Ag-NORs are located terminally pairs of small telocentric autosomes. The X on the smallest telocentric autosomes. chromosome is large and submetacentric and the small Y chromosome is telocentric. Order Primates Discussion Family Tarsiidae Tarsius syrichta. 2N = 80, FN = 94, Fig. The 2N = 40, FN = 76 karyotype of — 3A. Karyotypes of male Philippine tarsi- Podogymnura truei (Fig. lA) is the first re- ported for the gymnure subfamily Hylo- ers from Leyte Island include 6 pairs of small to large-sized metacentric or sub- myinae. It differs substantially from those of hedgehogs (subfamily Erinaceinae) metacentric autosomes and 33 pairs of which have relatively uniform karyotypes small to large-sized telocentric autosomes. The submetacentric X and minute Y chro- of 2N = 48, FN = 90-96 and X chromo- mosomes are, respectively, the largest and somes that are substantially larger than that & of P. truei (Gropp 1969, Bhatnagar El- smallest elements in the karyotype. Azawi 1978, Hubner et al. 1991, Reumer & Meylan 1986). Order Rodentia The widespread genus Crocidura dis- Family Sciuridae plays extensive interspecific chromosomal Sundasciurus philippinensis. 2N = 38, variation (Maddalena & Ruedi 1994, Zima — FN = 72, Fig. 3B. The karyotype of a et al. 1998). There are seven species of & male Philippine tree squirrel from Biliran Crocidura in the Philippines (Heaney VOLUME NUMBER 1 16, 3 703 AIAO (JHA fik/ii (0 tk AA OA AO *>> X X B ^alw 4^^ z^ ^ as* Bstf HM St Ik* S II e*^ ftti A*^ f SA 9|i it e* !t;$ ftii il X X Fig. 2. Karyotypes of Cynocephalus volans, female (USNM 458982), 2N = 38: A) standard, inset of Ag- NOR sites; B) G-banded. 704 PROCEEDINGS OF THE BIOLOGICAL SOCIETY OF WASHINGTON 9noi AO Al 0) Ofi u M M id la Ai An An «n od (II 0» A0 <^0 %l\ ft<^ A^ AO At ^ ftO »»* ^ h u u ft^ ^Jf 5t« A^ AA 5^ #S^ AJS ii^ X Y Fig. 3. Karyotypes of: A) Tarsius syrichta, male (EAR 1441), 2N = 80; B) Sundasciurus philippinensis, male (USNM 459821), 2N = 38. VOLUME 116, NUMBER 3 705 A X Y A# •• nt% *•• iiA HA XX If XI XX M X Y oiiA 16 II Fig. 4. Karyotypes of: A) Paradoxurus hermaphroditus, male (USNM 458891), 2N = 42; B) Viverra tan- galunga male (USNM 460000), 2N = 36. Ruedi 1994) of which two have been kar- limited data available suggest that the di- yotyped (this study). The 2N = 38, FN = versification of Philippine Crocidura has C 58 karyotype of grayi (Fig. IB) resem- not involved major chromosomal rearrange- bles those of several species with 2N = 38, ments of the sort seen for members of the FN = 54-58 from islands of the Sunda genus in Sulewesi (Ruedi & Vogel 1995), & Shelf and from Sulewesi (Ruedi Vogel or for Philippine rodents of the genus Apo- & & 1995). It also is similar to the presumed an- mys (Rickart Musser 1993, Rickart cestral arrangement for Crocidura (Mad- Heaney 2002). & dalena Ruedi 1994). The apparent simi- Suncus murinus is a chromosomally larity in the karyotypes of C. grayi and C. polymorphic species (2N = 30-40) found beatus is consistent with morphometric and throughout much of southeast Asia (Yosh- allozyme data that place these species as ida 1985, Zima et al. 1998). It occurs & sister-taxa (Heaney Ruedi 1994). The throughout the Philippines as a non-native 706 PROCEEDINGS OF THE BIOLOGICAL SOCIETY OF WASHINGTON commensal (Heaney et al. 1998), and on Leyte Island (Fig. 3A) is identical to those Negros Island, it also is naturalized and previously reported for specimens from & abundant in primary forest habitat (Heaney Mindanao (Boer Boer-Van der Vlist & et al. 1989). Both commensal and natural- 1973, Dutrillaux Rumpler 1988). Tarsius ized animals from Negros have identical bancanus also has 2N = 80, FN = 94 karyotypes of 2N = 40, FN = 60 (Fig. IC). (Klinger 1963), but its karyotype differs This same arrangement has been reported from that of T. syrichta in the size and rel- for specimens from much of southeast Asia ative arm lengths of several of the biarmed (Zima et al. 1998). Medina and Leonard autosomes. Tarsius dianae from central Su- (1977) reported a karyotype of 2N = 40, lawesi is the only other tarsier that has been FN = 54 for S. luzoniensis (a synonym of karyotyped. Its arrangement of 2N = 46, S. murinus) from Luzon Island. The differ- FN = 82 (Niemitz et al. 1991) differs from ence in FN compared to the Negros speci- those of T. syrichta and T. bancanus by mens most likely reflects variable assess- multiple Robertsonian and non-Robertso- ment of minute secondary arms on subtel- nian events. Chromosomal data support ocentric autosomes. phylogenetic hypotheses based on compar- The 2N = 38, FN = 40 karyotype of ative morphology and behavior that asso- Cynocephalus volans (Fig. 2), one of two ciate the Philippine and Sundaic species {T. members of the mammalian order Dermop- syrichta and T. bancanus) as relatively spe- tera, is reported here for the first time. This cialized forms separate from the three spe- also corrects an erroneous report by Hsu cies of Sulawesian tarsiers (Niemitz 1977, & and Benirschke (1973). They published Musser Dagosto 1987, Dagosto et al. identical karyotypes of 2N = 56, FN = 72 2001). for a specimen of Galeopterus variegatus The 2N = 38, FN = 72 karyotype of from Malaysia and for an animal at the Lin- Sundasciurus philippinensis (Fig. 3B) is re- coln Park Zoo, Chicago, originally identi- ported here for the first time. It is identical fied as C volans. After the latter died, it to that of S. jentinki, the only other member was sent to the Field Museum where it was of the genus that has been karyotyped (Har- accessioned and correctly identified as Gal- ada & Kobayashi 1980). Among callosci- eopterus (FMNH 60308; W. Stanley, pers. urine squirrels, Dremomys rufigenis and comm.). The two dermopterans have sub- Callosciurus albescens also share this ar- & stantially different karyotypes. Cynocephal- rangement (Nadler Hoffmann 1970, Har- & us lacks nine pairs of autosomes present in ada Kobayashi 1980), and several other Galeopterus, including seven pairs of small species of Callosciurus have karyotypes of to large-sized biarmed chromosomes, and 2N = 40, FN = 70-74 that differ only the X chromosome of the former is sub- slightly from that of S. philippinensis (Nad- metacentric whereas that of the latter is ler et al. 1975, Yong Hoi-Sen et al. 1975, metacentric (Fig. 2; Hsu & Benirschke Oshida & Yoshida 1999). The available 1973). The Ag-NORs of Cynocephalus are data suggest that callosciurines are chro- located on the smallest autosomal pair (Fig. mosomally conservative. 2). In Galeopterus, this same pair bears sec- A karyotype of 2N = 42, FN = 78 was & ondary constrictions (Hsu Benirschke reported previously for Paradoxurus her- 1973). This chromosomal distinctiveness is maphroditus from India (Ray-Chaudhuri et in accord with the substantial morphologi- al. 1966). The karyotype of Philippine cal and ecological differences that suggest specimens (Fig. 4A) is similar, but appears ancient divergence of the two species and to have fewer subtelocentric and more telo- supports their placement in separate genera centric elements (FN = 72). In other re- & (Stafford Szalay 2000). spects, the two karyotypes are identical. The karyotype of Tarsius syrichta from The 2N = 36, FN = 64 karyotype of — VOLUME 116, NUMBER 3 707 Viverra tangalunga (Fig. 4B) is the first re- baranza, L. Tag-at, and R. Utzurrum for as- ported for this widespread southeast Asian sistance with field work. W. Stanley species. Viverra zibetha, the only other (FMNH) provided information on the iden- member of this genus that has been exam- tity and history of the dermopteran speci- ined has a substantially different karyotype men formerly at Lincoln Park Zoo. Com- of 2N = 38 and FN = 68 (Pathak 1971). ments from L. Heaney and two anonymous Among members of the subfamily Viverri- reviewers helped improve the manuscript. nae that have been examined, Viverricula Permits and logistical support were provid- indica is the only species with 2N = 36 ed by the Philippine Protected Areas and & (Wurster Benirschke 1968). However, Wildlife Bureau and the Philippine Bureau Viverra tangalunga has more telocentric of Forestry Development. Field work was and fewer subtelocentric autosomes, and a supported by grants from the National Sci- significantly smaller Y chromosome than ence Foundation (BSR 8514223), the John does Viverricula. D. and Catherine T. MacArthur Foundation Interpretation of these chromosome data (90-09272A), and the Barbara Brown and is limited, in some cases, by the lack of Ellen Thorne Smith funds of the Field Mu- comparative information on related taxa. seum. Nonetheless, some general patterns of var- iation are apparent. Members of the endem- Literature Cited ic genera Podogymnura and Cynocephalus have karyotypes that differ substantially Bhatnagar, A. N., & T. F. El-Azawi. 1978. A karyotype from those of related taxa. In contrast, en- study of two species of hedgehogs, Hemiechin- demic species of Tarsius, Crocidura, and us auritus and Paraechinus aethiopicus (Insec- — Sundasciurus, and the widespread species tivora: Mammalia). Cytologia 43:53-59. Suncus murinus and Paradoxurus herma- Boer, L. E. M. de, & J. de Boer-Van der Vlist. 1973. The somatic chromosomes and the idiogram of phroditus have karyotypes that are similar, Tarsius syrichta carbonahus Huede, 1898 (Pri- — or identical, to those of closely related spe- mates: Tarsioidea). Genen en Phaenen 16:65- cies or conspecifics occurring elsewhere in 71. & Asia. These results mirror patterns of chro- Dagosto, M., D. L. Gebo, C. Dolino. 2001. Posi- mosomal variation documented for Philip- tional behavior and social organizat—ion of the Philippine tarsier (Tarsius syrichta). Primates pine bats and murid rodents (Rickart et al. 42:233-243. & 1999, Rickart Heaney 2002). Most en- Dobson, G. E. 1890. Descriptions of new species of — demic taxa have karyotypes that are unique Crocidura. Annals and Magazine of Natural compared to relatives occurring outside of History, series 6, 6:494-497. the Philippines. Some widespread species Dutrillaux, B., & Y. Rumpler. 1988. Absence of chro- mosomal similarities between tarsiers {Tarsius exhibit chromosomal polymorphism, in — syrichta) and other primates. Folia Primato- which Philippine populations have unique logica 50:130-133. karyotypes. The general pattern is one of Gray, J. E. 1832. On the family of Viverridae and its chromosomal rearrangement occurring as a generic sub-divisions, with an enumeration of — result of isolation. The degree to which this the species of several new ones. Proceedings of the Committee of Science and Correspon- pattern is expressed appears to be largely a dence of the Zoological Society of London function of how long a particular group has 1832(2):63-68. been present within the archipelago. Gropp, A. 1969. Cytologic mechanisms of karyotype evolution in insectivores. Pp. 247-266 in Com- parative mammalian cytogenetics. Springer, Acknowledgments Berlin, 473 pp. Harada, M., & T. Kobayashi. 1980. Studies on the I thank N. Antoque, R. Fernandez, S. small mammal fauna of Sabah, east Malaysia Goodman, L. Heaney, P. Heideman, J. II. Karyological analysis of some Sabahan Klompen, D. Samson, D. Schmidt, B. Ta- mammals (Primates, Rodentia, Chiroptera). — . 708 PROCEEDINGS OF THE BIOLOGICAL SOCIETY OF WASHINGTON Contributions from the Biological Laboratory, Miller, G. S., Jr. 1910. Descriptions oftwo new genera Kyoto University 26:83-95. and sixteen new species of mammals from the — Heaney, L. R., & M. Ruedi. 1994. A preliminary anal- Philippine Islands. Proceedings of the United ysis of biogeography and phylogeny of Croci- States National Museum 38:391-404. dura from the Philippines. Pp. 357-377 in J. Musser, G. G., & M. Dagosto. 1987. The identity of Meritt, G. Kirkland, & R. Rose, eds.. Advances Tarsius pumilus, a pygmy species endemic to in the biology of shrews. Special Publication the montane mossy forests of central Sulawe- — 18, Carnegie Museum of Natural History, Pitts- si. American Museum Novitates 2867:1-53. burgh, 458 pp. Nadler, C. F, & R. S. Hoffmann. 1970. Chromosomes , P D. Heideman, E. A. Rickart, R. C. B. Ut- of some Asian and So—uth American squirrels zurrum, & J. S. H. Klompen. 1989. Elevational (Rodentia: Sciuridae). Experientia 26:1383- zonation of mammals in the central Philip- 1386. — pines. Journal of Tropical Ecology 5:259- , , & M. E. Hight. 1975. Chromosomes 280. of three species of Asian tree squirrels Callos- — , et al. 1998. A synopsis of—the mammalian ciurus (Rodentia: Sciuridae). Experientia 31: fauna ofthe Philippine Islands. Fieldiana: Zo- 166-167. ology, n.s. 88:1-61. Niemitz, C. 1977. Zur Funktionsmorphologie und Howell, W. M., & D. A. Black. 1980. Controlled silver Biometrie der Gattung Tarsius Storr, 1780. Her- staining of neucleolar organizer regions with a leitung von Evolutionsmechanismen bei einem — protective colloidal developer: a 1-step meth- Primaten. Courier der Senckenbergischen Na- — od. Experientia 36:1014-1015. turforschenden Gesellschaft 25:1-161. Hsu, T C. & K. Benirschke. 1973. Cynocephalus var- , A. Nietsch, S. Warter, & Y Rumpler. 1991. iegatus, C. volans (flying lemur) 2n = 56. An Tarsius dianae: a new primate species from — atlas ofmammalian chromosomes. Vol. 7, Folio central Sulawesi (Indonesia). Folia Primato- 303, Springer-Verlag, New York, unpaged. logica 56:105-116. Hubner, R., T Maddalena, & W. Poduschka. 1991. The Oshida, T, & M. C. Yoshida. 1999. Chromosomal lo- karyotype ofthe middle-African hedgehog Ate- calization of nucleolus organizer regions in — lerix albiventris Wagner, 1841 and its cytotax- eight Asian squirrel species. Chromosome onomical relationships to other Erinaceinae (In- Science 3:55-58. — sectivora: Erinaceidae). Genetica 83:243-246. Pallas, P S. 1777. Pg. 426 in Schreber, J. C. D. von. Klinger, H. P. 1963. The somatic chromosomes of 1774-1785. Die Saugethier in Abbildungen some primates (Tupaia glis, Tarsius bancanus, nach der Natur mit Beshreibungen. Erlangen Cercoc—ebus aterrimus, Symphalangus syndac- Wolfgang Walden, 1112 pp. tylus). Cytogenetics 2:140-151. Pathak, S. 1971. Karyotype ofthe Oriental Civet, Viv- Linnaeus, C. 1758. Systema naturae per regna tria na- erra zibetha, Linn. (Viverridae-Carnivora). turae, secundum classes, ordines, genera, spe- Mammalian Chromosomes Newsletter 12(2):61. cies, cum characteribus, differentiis, synonymis, Patton, J. L. 1967. Chromosome studies of certain locis, 10th edition. Laurentius Salvius, Stock- pocket mice, genus Perognathus (Rodentia: — holm 1:1-824. Heteromyidae). Journal of Mammalogy 48: . 1766. Systema naturae per regna tria naturae, 27-37. secundum classes, ordines, genera, species, cum Ray-Chaudhuri, S. P, P V. Ranjini, & T Sharma. 1966. characteribus, differentiis synonymis, locis, Somatic chromosomes of the common palm 12th edition. Laurentius Salvius, Stockholm 1: cive—t, Paradoxur—us hermaphroditus (Viverri- 1-532. dae Camivora). Experientia 22:740-741 Maddalena, T, & M. Ruedi. 1994. Chromosomal evo- Reumer, W. F, & A. Meylan. 1986. New developments lution in the genus Crocidura (Insectivora: Sor- in vertebrate cytotaxonomy IX: chromosome icidae). Pp. 335-344 in J. Merritt, G. Kirkland, numbers in the order Insectivora (Mamma- & R. Rose, eds., Advances in the biology of lia).—Genetica 70:119-151. shrews. Special Publication 18, Carnegie Mu- Rickart, E. A., & L. R. Heaney. 2002. Further studies seum of Natural History, Pittsburgh, 458 pp. on the chromoso—mes ofPhilippine rodents (Mu- Mearns, E. A. 1905. Description of some new genera ridae: Murinae). Proceedings ofthe Biological and species ofmammals from the Philippine Is- Society of Washington 115:473-487. — lands. Proceedings of the United States Na- & G. G. Musser. 1993. Philippine rodents: , tional Museum 28:425-460. chromosomal characteristics and their signifi- Medina, F I. S., & A. Leonard. 1977. Observations sur cance for phylogenetic inference am—ong 13 spe- les chromosomes de Suncus luzoniensis Pe- cies (Rodentia: Muridae: Murinae). American — ters. Acta Zoologica et Pathologica Antver- Museum Novitates 3064:1-34. piensia 69:183-188. , L. R. Heaney, & M. J. Rosenfeld. 1989. Chro-