taxonID	type	description	language	source
03DC6055C158FFEB52E2CC860DA3FB8F.taxon	discussion	CONTENT AND CONTEXT. Order Rodentia, suborder Sciuromorpha, family Sciuridae, subfamily Callosciurinae, genus Callosciurus. Number of subspecies is not known. Most named forms are distinguished based on coat color patterns, yet these are highly variable and may not indicate subspecific distinction. We found 64 named forms with 16 unintended misspellings and 4 unambiguous synonyms; thus, a total of 44 subspecies is possible. Alphabetically, these 44 names with parenthetical synonyms or misspellings are: armalis Lyon, 1911; atricapillus Schlegel, 1863 (= atrocapillus Gray, 1867); atrox Miller, 1913; baluensis Bonhote, 1901; bangkanus Schlegel, 1863 (= bankana Anderson, 1878; bangkannus Heaney, 1978); banksi Chasen, 1933; baramensis Chasen, 1940; borneoensis Müller and Schlegel, 1842 (= borneonensis Gray, 1867; borneensis Payne et al., 1985); caedis Chasen and Kloss, 1932; carimatae Miller, 1906 a; carimonensis Miller, 1906 b; caroli Bonhote, 1901; condurensis Miller, 1906 b; coomansi Sody, 1949; erythromelas Temminck, 1853; griseicauda Bonhote, 1901; harrisoni Stone and Rehn, 1902; humei Bonhote, 1901; kuchingensis Bonhote, 1901; medialis Allen and Coolidge, 1940; melanops Miller, 1902; mendanauus Lyon, 1906 (1907); mimellus Miller, 1900 (= mimelus Robinson and Kloss, 1918); mimiculus Miller, 1900; navigator Bonhote, 1901; nyx Lyon, 1908 b; palustris Lyon, 1908 a; pelapius Lyon, 1911 (pelapis Robinson and Kloss, 1918); penialius Lyon, 1908 b; piceus Peters, 1866 (= erebus Miller, 1903); pluto Gray, 1867; prevostii Desmarest, 1822 (= prevosti Thomas and Hartert, 1894; indica Müller and Schlegel, 1842; typicus Bonhote, 1901); proserpinae Lyon, 1907 (proscipinae Sody, 1949; prosperinae Corbet and Hill, 1992); rafflesii Vigors and Horsfield, 1828 (= rafflesi Ellermann, 1940); redimitus van der Boon Mesch, 1829; rufogularis Gray, 1842; rufonigra Gray, 1842 (= rufoniger Motley and Dillwyn, 1855); sanggaus Lyon, 1908 a; sarawakensis Gray, 1867 (sarwakensis Anderson, 1878); schlegelii Gray, 1867 (= erythrogenys Schlegel, 1863; schlegeli Bonhote, 1901); suffusus Bonhote, 1901; sumatranus Schlegel, 1863 (= sumatrana Anderson, 1878); waringensis Sody, 1949 (= waringentis Sody, 1949); wrayi Kloss, 1910.	en	Lurz, Peter W. W., Fielding, Isabella, Hayssen, Virginia (2017): Callosciurus prevostii (Rodentia: Sciuridae). Mammalian Species 49 (945): 40-50, DOI: 10.1093/mspecies/sex004, URL: http://dx.doi.org/10.1093/mspecies/sex004
03DC6055C158FFEB52E2CC860DA3FB8F.taxon	description	NOMENCLATURAL NOTES. The generic name, Callosciurus, often translated as “ beautiful squirrel, ” is from the Greek callo for beautiful, skia for shadow, and oura for tail (Borror 1960; Lurz et al. 2005). The species name, prevostii, honors the French geologist, Constant Prévost. Other common names are black squirrel (Davis 1962), tupai labang, tupai chelum, tupai bekarang (Banks 1931), and tricolored squirrel (Heaney 1978). The above 44 named forms or subspecies associated with prevostii (64 names minus 16 misspellings minus 4 unambiguous synonyms) vary with those summarized in the literature: Robinson and Kloss (1918): 35 subspecies (excludes banksi, baramensis, caedis, coomansi, indica, medialis, redimitus, rufogularis, sumatranus, waringensis; treat schlegelii = erythrogenys, piceus = erebus); Chasen (1940): 34 subspecies (excludes coomansi, erythrogenys = schlegelii, erythromelas, indica, kuchingensis, medialis, mimellus, redimitus, rufogularis, sumatranus, waringensis; treats piceus = erebus); Ellermann (1940): 39 subspecies (excludes baramensis, coomansi, indica, medialis, rufogularis, waringensis; treats schlegelii = erythrogenys, piceus = erebus); Heaney (1978): 39 subspecies (excludes indica, kuchingensis, medialis, redimitus, rufogularis, sumatranus; treats schlegelii = erythrogenys, piceus = erebus); Corbet and Hill (1992): 40 named forms (excludes baluensis, baramensis, erythromelas, medialis, schlegelii = erythrogenys, suffusus; includes both erebus and piceus); Thorington and Hoffmann (2005): 44 named forms (excludes baluensis, baramensis, medialis; treat schlegelii = erythrogenys; includes both piceus and erebus, as well as both rufonigra and rufoniger).	en	Lurz, Peter W. W., Fielding, Isabella, Hayssen, Virginia (2017): Callosciurus prevostii (Rodentia: Sciuridae). Mammalian Species 49 (945): 40-50, DOI: 10.1093/mspecies/sex004, URL: http://dx.doi.org/10.1093/mspecies/sex004
03DC6055C158FFEB52E2CC860DA3FB8F.taxon	diagnosis	DIAGNOSIS Callosciurus prevostii typically has a tricolored pattern with a black or dark back and red belly separated by a distinct white stripe (Fig. 1). This pelage character readily distinguishes this species from other sympatric, medium-sized tree-squirrels. Several species of Sundasciurus co-occur with C. prevostii, but, where they do so, they are either smaller in size (length of head and body <200 mm versus> 200 mm) or different in color with either a reddish back or a gray to white venter (Payne et al. 1985; Corbet and Hill 1992). C. prevostii also overlaps on the Malayan Peninsular with C. caniceps (gray-bellied squirrel), C. erythraeus (Pallas’s squirrel), and C. notatus (plantain squirrel — Thorington et al. 2012; Lurz et al. 2013). These species do not have the rufous venter of C. prevostii.	en	Lurz, Peter W. W., Fielding, Isabella, Hayssen, Virginia (2017): Callosciurus prevostii (Rodentia: Sciuridae). Mammalian Species 49 (945): 40-50, DOI: 10.1093/mspecies/sex004, URL: http://dx.doi.org/10.1093/mspecies/sex004
03DC6055C158FFEB52E2CC860DA3FB8F.taxon	description	GENERAL CHARACTERS Callosciurus prevostii is a medium-sized tree-squirrel without sexual dimorphism. Mean external measurements (mm or g, parenthetical n) for female and male C. prevostii, respectively, from Borneo were: total length, 477 (6), 469 (4); tail length, 243 (6), 231 (4); body mass, 433 (7), 439 (4 — Banks 1931). Mean external measurements (mm, n, mixed sexes) from Banka and Mendanau (islands between Borneo and Sumatra) were: length of head and body, 249.4 (16); length of tail vertebrae, 229.1 (15); hind foot length, 57.3 (16 — Lyon 1906 (1907 )). Mean external measurements (mm, n) for female and males, respectively, from Sumatra were: length of head and body, 264.0 (27), 263.5 (29); length of tail vertebrae, 256.6 (27), 251.56 (29); hind foot length, 64.3 (24), 64.0 (25 — Lyon 1908 b). Mean external measurements (mm, n) for females and males, respectively, from Borneo and adjacent islands were: length of head and body, 248.1 (44), 241.6 (46); length of tail vertebrae, 233.3 (43), 230.9 (45); hind foot length 59.5 (44), 59.2 (46 — Lyon 1908 a, 1911). Mean external measurements (mm, n) for adults of mixed sex from the north China Sea, Sumatra, Karimata Islands, Rhio-Linga archipelago, and Borneo were: length of head and body, 239.5 (63); length of tail vertebrae, 220.8 (63); hind foot length, 52.1 (63 — Miller 1900, 1902, 1903, 1906 a, 1906 b, 1913). Mean percent of tail relative to length of head and body for 275 C. prevostii from multiple subspecies was 95.6 % (range 69 – 128 — Sody 1949). At Samarakan, a single adult male representing the subspecies C. p. caroli was received from a local hunter (total length, 51; body mass, 360 g — Bonhote 1901). Body mass is 250 – 500 g in Borneo (Payne et al. 1985). Mean cranial measurements (mm, n, Fig. 2) from C. p. atricapillus and C. p. pluto were: greatest length of skull, 54.9 (8); length from condyles to gnathion, 47.6 (8); basicranial length, 47.8 (8); zygomatic width, 34.3 (9); greatest breadth of braincase, 24.1 (9); least interorbital breadth, 22.1 (9); least postorbital breadth, 19.1 (9); length of nasals medially, 16.5 (9); breadth of combined nasals anteriorly, 8.1 (9); breadth of combined nasals posteriorly, 4.5 (3); diastema, 13.0 (9); length of foramina incisive, 3.1 (3); length of upper toothrow, 10.4 (9 — Glydenstolpe 1919). Cranial and mandibular measurements (mm) of the male type of C. p. mendanauus were: greatest length, 54; basal length, 46.5; basilar length, 43.5; palatilar length, 23.5; diastema, 13.5; zygomatic breadth, 33; interorbital constriction, 22; least depth of ramus of mandible in front of toothrow, 5; maxillary toothrow, 11.25; mandibular toothrow, 11 (Lyon 1906 (1907 )). Mean cranial measurements (mm, n) for other male and female C. prevostii from Banka and Mendanau were: upper length of skull, 55.1 (14); zygomatic breadth, 34.2 (14); interorbital constriction, 22.9 (14); length of upper toothrow (alveoli), 8.5 (16 — Lyon 1906 (1907 )). Mean cranial measurements (mm, n) for females and males, respectively, from Sumatra were: greatest length of skull, 58.21 (27), 58.28 (29); interorbital constriction, 23.58 (27), 23.39 (29); zygomatic breadth, 35.78 (25), 35.21 (28 — Lyon 1908 b). Mean cranial measurements (mm, n) for females and males, respectively, from Borneo and adjacent islands were greatest length of skull, 55.68 (43), 54.90 (44); interorbital constriction, 22.16 (44), 21.85 (44); zygomatic breadth, 33.80 (42), 33.27 (44 — Lyon 1908 a, 1911). Mean cranial measurements (mm, n) for adults of both sexes from the north China Sea, Sumatra, Karimata Islands, Rhio-Linga archipelago, and Borneo were greatest length of skull, 54.7 (8); basal length (or condylobasilar length), 47.9 (9); basilar length, 44.6 (8); palatal length, 23.6 (6); diastema, 13.0 (5); length of nasals, 16.9 (7); breadth of nasals anteriorly, 8.3 (4); breadth of nasals posteriorly, 4.8 (3); interorbital breadth (or interorbital constriction), 21.9 (9); breadth between tips of postorbital processes, 29.5 (3); zygomatic breadth, 33.6 (9); mastoid breadth, 22.1 (3); breadth of palate between premolars, 7.1 (3); depth of rostrum at posterior extremity of nasals, 12.7 (3); mandibular length, 34.7 (9); depth of mandible at posterior root of large premolars, 8.1 (3); maxillary toothrow, 10.5 (9); breadth across both upper incisors together at rim of alveoli, 5.2 (3); mandibular toothrow, 10.5 (9 — Miller 1900, 1902, 1903, 1906 a, 1906 b, 1913). Mean length (mm) of the upper toothrow for 112 C. prevostii from multiple subspecies was 10.58 (range 9.0 – 11.6 — Sody 1949). Callosciurus prevostii has many color variations, but all individuals have red bellies (Payne et al. 1985), and the dorsum is usually black. The back and belly are often separated by a white or fawn stripe of variable width (Banks 1978).	en	Lurz, Peter W. W., Fielding, Isabella, Hayssen, Virginia (2017): Callosciurus prevostii (Rodentia: Sciuridae). Mammalian Species 49 (945): 40-50, DOI: 10.1093/mspecies/sex004, URL: http://dx.doi.org/10.1093/mspecies/sex004
03DC6055C158FFEB52E2CC860DA3FB8F.taxon	distribution	DISTRIBUTION Callosciurus prevostii occurs (Fig. 3) on the Isthmus of Kra in southern Thailand, south through Sumatra and Borneo (including nearby islands), and east to Sulawesi (Corbet and Hill 1992; Wilson et al. 2006; Thorington et al. 2012). Corbet and Hill (1992) specifically list the islands of Kundur, Great Karimon (Riau Island), Rupat, Penjalei, Bangka, Mendanau (Sumatra), Wai, Saint Barbe (Tambelan Island), Serasan (South Natuna Island), Karimata, Sanggau, Temaju, Panebangan, Pelapis, Labuan, Bangi, and Balembangan (Borneo). Its occurrence in northern Sulawesi (erythromelas, erythrogenys = schlegelii) is considered “ extralimital ” by Laurie and Hill (1954: 92) and “ introduced ” by Musser (1987: 80) based on Laurie and Hill (1954). Rather than subspecies, known type localities for the 44 named forms are given on the distribution map (Fig. 3) because ambiguities in the literature make the distributions of subspecies uncertain.	en	Lurz, Peter W. W., Fielding, Isabella, Hayssen, Virginia (2017): Callosciurus prevostii (Rodentia: Sciuridae). Mammalian Species 49 (945): 40-50, DOI: 10.1093/mspecies/sex004, URL: http://dx.doi.org/10.1093/mspecies/sex004
03DC6055C158FFEB52E2CC860DA3FB8F.taxon	description	FORM AND FUNCTION The iris is dark brown (Banks 1931). The “ thumb ” has a nail rather than a claw (Banks 1931). Claws are paler at their tips (Banks 1931). An illustration of the baculum is available (Davis 1962; see also Corbet and Hill 1992). Three pairs of mammae are present (Moore 1961; Davis 1962). The tail is “ of the fluebrush variety, hairs sticking out at right angles rom the long axis of the tail and not feathery and flattened ” (Banks 1931: 45). Body size is related to island size. “ The smallest squirrels occur on the smallest islands and increase in body size on islands up to about 104 km 2. ” On larger islands, “ body size decreases significantly as island area increases ” (Heaney 1978: 41 – 42). ONTOGENY AND REPRODUCTION Average litter size from 9 litters was 1.55 young with a range of 1 to 3 (Hayssen et al. 1993). Five gestations were 46 – 48 days (Hayssen et al. 1993). In north Borneo, pregnant females were found in June and August, and a lactating female was found in August (Davis 1962). Lactating females were found the first 3 months of the year in Borneo (Banks 1931). Two neonates weighed 15.9 and 16.8 g (Hayssen et al. 1993). “ Newborn young are altricial, hairless and grey with leathery skin and a thick membrane covering their eyes ” (Xanten et al. 1988: 284). Although without fur, pigmentation of the black back and chestnut belly were visible at age 14 days in a captive Callosciurus prevostii (Edwards 1978). Lateral stripe is pink in the juvenile rather than white as in adult pelage (Edwards 1978). Eyes open by 22 days after birth (Xanten et al. 1988).	en	Lurz, Peter W. W., Fielding, Isabella, Hayssen, Virginia (2017): Callosciurus prevostii (Rodentia: Sciuridae). Mammalian Species 49 (945): 40-50, DOI: 10.1093/mspecies/sex004, URL: http://dx.doi.org/10.1093/mspecies/sex004
03DC6055C158FFEB52E2CC860DA3FB8F.taxon	biology_ecology	ECOLOGY Population characteristics. — Population size fluctuate between years and seasons. Peak abundance in dipterocarp dominated, lowland primary forest in Sarawak, Malaysia occur after the peak of fruiting (Nakagawa et al. 2007). Of 4 sympatric Callosciurus species, C. prevostii is the 2 nd most abundant in the Ulu Mida Forest Reserve, Kedah, Malaysia with an estimated overall density of 3.29 km− 2 (Saiful and Nordin 2004). The estimate of 2.98 km− 2 from hill dipterocarp production forest in Sarawak (Zainuddin 1996, not seen, cited in Saiful and Nordin 2004) is low compared to estimates of 14.6 km− 2 from lowland dipterocarp forest in central Kalimantan, Indonesia (McConkey and Chivers 2004). C. prevostii was present both before and after selective logging in a dipterocarp forest (Dahaban et al. 1996). Callosciurus prevostii occurs in tall and secondary forests but will enter gardens and plantations (Payne et al. 1985). It occupies the middle story of the forest (Banks 1978). In Malaysia, C. prevostii was trapped in primary lowland forest dominated by dipterocarp trees in the emergent and canopy layers and species of Euphorbiaceae, Burseraceae, and Myristicaceae in the understory (Nakagawa et al. 2007). In this habitat, animals forage predominantly in the canopy but were occasionally observed on the ground (Nakagawa et al. 2007). In Selangor, oil palm estates are preferred habitat (Harrison and Traub 1950). At Sarawak from an area of disturbed logged forest interspersed with forest plantation of Acacia mangium, a specimen of C. p. sarawakensis was obtained from a local hunter (Wilson et al. 2006). C. p. pluto inhabits primary and old logged forests rather than clearings, newly logged forests, cultivated areas, or towns (Davis 1962). Diet. — Callosciurus prevostii pluto eats arthropods (5 – 40 %; ants, termites, and beetle larvae), as well as fruits and nuts (Davis 1962; Banks 1978; Payne et al. 1985). Finely divided pieces of pulpy fruits were present in the stomachs of 5 animals (Davis 1962). C. prevostii eats flowers and fruits of Gonystylus bancanus (Ismail et al. 2011) and fruits of Durio (Nakashima et al. 2008). In a captive zoo setting, feral mice were eaten (Xanten et al. 1988). Diseases and parasites. — Knowledge about parasites and diseases in this species is highly limited. Two captive animals lived 19 years, 2 months and 21 years, 1 month (Weigl 2005; Gorbunova et al. 2008). Endoparasites include Eimeria callosciuri in Callosciurus prevostii from Malaysia (Colley 1971) and alveolar echinococcosis, caused by the fox tapeworm Echinococcus multilocularis. The latter was detected in a C. p. borneoensis found dead in an outdoor enclosure at Zürich Zoo (Staebler et al. 2007). C. prevostii tested positive for eggs of Dicrocoelium dendriticum, Capilaria hepatica, an unidentified Strongyloides species, a pinworm (Syphacia), a gastrointestinal nematode (described as “ Nippostrongylus-like ”), and the cestode Hymenolepsis diminuta (D’Ovidio et al. 2014, 2015). BEHAVIOR Callosciurus prevostii is arboreal, only descending to the ground to cross gaps in the trees, and diurnal, with most activity in the early morning and late afternoon (Davis 1962; Payne et al. 1985). C. prevostii does not curl its tail over its back but carries it unbent behind and somewhat upwards (Banks 1931). When animals move, the forefeet are splayed out horizontally, whereas the hind feet are vertical (Banks 1931). When animals sit, the ischial region touches the back of the leg rather than the substrate (Banks 1931). The large, magpie-like nest has a thick outer layer of fairly big sticks and an inner layer lined with shredded bark and a few grass-like bents; the entrance is usually low on one side of the bundle (Banks 1931). Young are “ carried in the mouth by the scruff of the neck like a cat with a kitten ” (Banks 1931: 46). Callosciurus prevostii does not emit bird-like whistles but has a call described as “ a series of chuckles ” (Banks 1978: 199). It is active and noisy (Banks 1931). When eating, “ the food is held between the palms of the two ‘ hands’ and pieces chipped off by the lower pair of incisor teeth working against the upper pair ” (Banks 1931: 46). In captivity, “ prior to mating the male chases the female, emitting clicking and high-pitch ‘ twitter’ vocalisations to which she responds with a high-pitched twitter and screeches as the pursuit continues. This behavior continues for three to four-and-a-half hours with as many as ten mating encounters taking place, each encounter including one to three copulations ” (Xanten et al. 1988: 284).	en	Lurz, Peter W. W., Fielding, Isabella, Hayssen, Virginia (2017): Callosciurus prevostii (Rodentia: Sciuridae). Mammalian Species 49 (945): 40-50, DOI: 10.1093/mspecies/sex004, URL: http://dx.doi.org/10.1093/mspecies/sex004
03DC6055C158FFEB52E2CC860DA3FB8F.taxon	description	GENETICS Diploid number (2 n) of chromosomes is 40 with a fundamental number (FN) of 70. Autosomal chromosomes include 6 pairs of metacentrics, 10 pairs of submetacentrics, and 3 pairs of acrocentrics (Oshida and Yoshida 1994). The medium-sized X chromosome is submetacentric and the small Y chromosome is metacentric (Yong et al. 1975; Oshida and Yoshida 1994; Oshida et al. 1996). Cytochrome b sequences were used to investigate both the phylogenetic relationships of several Callosciurus species (Oshida et al. 2001, 2011) and the phylogeographical characteristics of C. prevostii in southeast Asia (Oshida et al. 2016). In both phylogenetic analyses, C. prevostii formed a well-supported lineage with C. nigrovittatus, the black-striped squirrel. Two nuclear genes (c-myc and RAG 1) were sequenced from C. prevostii (Steppan et al. 2004). Novel sequences for RNase 1, a gene which encodes secretory proteins, were identified in 4 squirrel species including C. prevostii (Siegel et al. 2009).	en	Lurz, Peter W. W., Fielding, Isabella, Hayssen, Virginia (2017): Callosciurus prevostii (Rodentia: Sciuridae). Mammalian Species 49 (945): 40-50, DOI: 10.1093/mspecies/sex004, URL: http://dx.doi.org/10.1093/mspecies/sex004
03DC6055C158FFEB52E2CC860DA3FB8F.taxon	conservation	CONSERVATION The International Union for the Conservation of Nature and Natural Resources Red List of Threatened Species lists Callosciurus prevostii as a species of “ Least Concern ” not only because it is common and widely distributed, but also because it is somewhat tolerant of habitat modification (Duckworth and Hedges 2008). However, the population trend is decreasing, and the remaining lowland habitat is under threat. In addition, the species is heavily hunted in parts of Sarawak for the pet trade (Duckworth and Hedges 2008).	en	Lurz, Peter W. W., Fielding, Isabella, Hayssen, Virginia (2017): Callosciurus prevostii (Rodentia: Sciuridae). Mammalian Species 49 (945): 40-50, DOI: 10.1093/mspecies/sex004, URL: http://dx.doi.org/10.1093/mspecies/sex004
