Transandinomys talamancae
Transandinomys talamancae | |
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Skull of a male from Gatun, Panama, seen from above[1] | |
Scientific classification | |
Domain: | Eukaryota |
Kingdom: | Animalia |
Phylum: | Chordata |
Class: | Mammalia |
Order: | Rodentia |
Family: | Cricetidae |
Subfamily: | Sigmodontinae |
Genus: | Transandinomys |
Species: | T. talamancae
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Binomial name | |
Transandinomys talamancae (J.A. Allen, 1891)
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Distribution of Transandinomys talamancae in southern Central America and northwestern South America[3] | |
Synonyms[13] | |
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Transandinomys talamancae is a
The species was first described in 1891 by
Active during the night, Transandinomys talamancae lives on the ground and eats plants and insects. Males move more and have larger
Taxonomy
In 1891, Joel Asaph Allen was the first to scientifically describe Transandinomys talamancae, when he named Oryzomys talamancae from a specimen from Talamanca, Costa Rica. He placed it in the genus Oryzomys, then more broadly defined than it is now, and compared it to both the marsh rice rat (O. palustris) and to O. laticeps.[14] Several other names that are now recognized as synonyms of Transandinomys talamancae were introduced in the following years. In 1899, Allen described Oryzomys mollipilosus, O. magdalenae, and O. villosus from Magdalena Department, Colombia.[15] Oldfield Thomas added O. sylvaticus from Santa Rosa, Ecuador in 1900[16] and O. panamensis from Panama City, Panama, in 1901.[17] In the same year, Wirt Robinson and Markus Lyon named Oryzomys medius from near La Guaira, Venezuela.[18] Allen added O. carrikeri from Talamanca, Costa Rica, in 1908.[19]
In 2006, Marcelo Weksler published a
Several common names have been proposed for Transandinomys talamancae, including "Talamanca Rice Rat",[31] "Transandean Oryzomys",[32] and "Talamancan Rice Rat".[2]
Description
Transandinomys talamancae is a medium-sized, brightly colored rice rat.[33] It is similar to T. bolivaris and the two are often confused.[34] They are about as large, but in T. talamancae the tail is longer and the hindfeet shorter.[35] Both species share uniquely long vibrissae, with both the mystacial (above the mouth) and superciliary vibrissae extending to or beyond the back margin of the ears when laid back against the head, but those in T. bolivaris are substantially longer.[12] H. alfaroi, a widespread species ranging from Mexico to Ecuador, is also similar.[36] It is smaller and darker, but young adult T. talamancae are similar in color to adult H. alfaroi and often misidentified.[37] Hylaeamys megacephalus,[Note 1] with which T. talamancae was synonymized for some decades, is similar in body size, but is not known to overlap with T. talamancae in range.[39]
The fur is short, dense and soft in Transandinomys talamancae;
Country | n[Note 2] | Head and body | Tail | Hindfoot | Ear |
---|---|---|---|---|---|
Panama | 22 | 124.4 (101–136) | 124.7 (110–143) | 29.2 (27–32) | 21.1 (16–25) |
Colombia | 13 | 135.2 (120–151) | 125.2 (114–140) | 29.5 (27–32) | 19.0 (18–22) |
Ecuador | 20[Note 3] | 124 (118–136) | 128.5 (118–137) | 29.1 (28–31) | – |
Measurements are in millimeters and in the form "average (minimum–maximum)". |
The sparsely haired tail is approximately as long as the head and body.[45] It is dark brown above and lighter below.[40] In contrast, the tail of H. megacephalus has little to no difference in color between the upper and lower surface.[43] In 2006, Weksler and colleagues noted tail coloration as a difference between the two species of Transandinomys (bicolored in T. talamancae and unicolored in T. bolivaris),[12] but in their 1998 study, Musser and colleagues could not find differences in tail coloration between their Panamanian samples of the two species.[47]
The hindfeet are long and have the three central digits longer than the two outer ones.
The length of the head and body is 105 to 151 mm (4.1 to 5.9 in), tail length 105 to 152 mm (4.1 to 6.0 in), hindfoot length 26 to 32 mm (1.0 to 1.3 in), ear length 17 to 24 mm (0.67 to 0.94 in), and body mass 38 to 74 g (1.3 to 2.6 oz).
Skull and teeth
The skull has a long rostrum (front part), a broad
The
The
The upper incisor is
Male reproductive anatomy
As is characteristic of Sigmodontinae, Transandinomys talamancae has a complex penis, with the distal (far) end of the baculum (penis bone) ending in a structure consisting of three digits.[71] As in most oryzomyines, the central digit is larger than the two at the sides.[72] The outer surface of the penis is mostly covered by small spines, but there is a broad band of nonspinous tissue.[73]
Some features of the accessory glands in the male genital region vary among oryzomyines. In Transandinomys talamancae,
Karyotype
The
The karyotype of an Ecuadorean sample from north of the Gulf of Guayaquil is similar to that of Venezuelan animals at 2n = 36, FN = 60; it includes four acrocentric and two subtelocentric pairs and no submetacentrics. In contrast, a sample from south of the Gulf had 2n = 54, FN = 60, including 23 pairs of acrocentrics and four pairs of metacentrics (with two equally long arms). Musser and colleagues termed the difference between the two Ecuadorian forms "impressive"[80] and noted that further research was needed to understand the karyotypic differentiation within the species more fully.[81] Both T. bolivaris and H. alfaroi have more chromosomes and arms, at 2n = 58, FN = 80 and 2n = 60–62, FN = 100–104 respectively.[82] Hylaeamys megacephalus has 2n = 54, FN = 58–62 and the similar Hylaeamys perenensis has 2n = 52, FN = 62; these karyotypes resemble that of southern Ecuadorean T. talamancae.[83]
Distribution and habitat
The distribution of Transandinomys talamancae extends from northwestern Costa Rica south and east to northern Venezuela and southwestern Ecuador, up to 1,500 m (5,000 ft) above sea level.
Transandinomys talamancae reaches the northern limit of its range in Costa Rica, but except for one record from the far northwest (in Guanacaste Province near the southern margin of Lake Nicaragua), it is known only from the southeastern third of the country. In contrast, T. bolivaris and H. alfaroi occur further north, into Honduras and Mexico respectively. It occurs throughout Panama at low elevations. Along the Pacific coast in Colombia and Ecuador, it is found on the coastal plain and the adjacent foothills of the Andes.[85] The southernmost known record is in far southwestern Ecuador, but the species may range into nearby Peru.[84]
It also occurs throughout northern Colombia at low elevations and into western Venezuela west of Lake Maracaibo and at the foot of the western part of the Venezuelan Coastal Range east to Guatopo National Park.[85] Hylaeamys megacephalus occurs further to the east in the eastern portion of the coastal range, separated by the coastal Eastern Caribbean Dry Zone.[43] There is a record from the Orinoco Delta of northeastern Venezuela, well within the range of Hylaeamys megacephalus, but Musser and colleagues suggest that this is based on mislabeled specimens.[86] The species has also been found on the narrow strip between the Llanos and the Andes (Cordillera Oriental and Cordillera de Mérida) in eastern Colombia and northwestern Venezuela.[85] The unforested Llanos separate these areas from Hylaeamys populations. Hylaeamys perenensis[Note 6] does, however, occur further south along the eastern foothills of the Cordillera Oriental in Colombia and it is possible that the two overlap in this area.[43]
Ecology and behavior
Transandinomys talamancae is a common, even abundant, species.
Males tend to travel longer distances than females. The average home range size in Fleming's study was 1.33 hectares (3.3 acres); males had larger home ranges on average.[92] Specimens that were once captured tended to be captured more frequently than those that had never been captured.[93] Fleming estimated that population densities reached peaks of up to 4.3 per ha (1.7 per acre) late in the rainy season (October–November), but dropped to near zero around June; however, these figures may well be underestimates.[94] In central Venezuela, population densities vary from 5.5 to 9.6 per ha (2.2 to 3.8 per acre).[95]
In Panama, this species breeds year-round without apparent seasonal variability.
Ten species of mites (
Conservation status
A widespread and common species, Transandinomys talamancae is listed as "
Notes
- ^ Oryzomys megacephalus, as used by Musser et al. (1998), was more broadly defined than the current Hylaeamys megacephalus (it was transferred to the new genus Hylaeamys by Weksler and colleagues in the same 2006 paper that introduced Transandinomys); in their definition, it occurred throughout Amazonia and north to Trinidad and south to Paraguay.[37] However, western Amazonian populations of the species have since been separated into a different species, Hylaeamys perenensis. In the following comparisons, based on Musser et al. (1998) who did not separate the two, only H. megacephalus is mentioned, but both species are morphologically virtually identical and are known to differ only in size, karyotype, and mitochondrial DNA sequences.[38]
- ^ Number of specimens measured.
- ^ 19 for tail length.
- ^ The male accessory glands of T. talamancae, and of a number of other sigmodontines, were described by Voss and Linzey (1981). Their sample of "Oryzomys capito" included specimens from Panama and Trinidad, representing Transandinomys talamancae and Hylaeamys megacephalus, respectively, but their description can be applied to both.[74]
- ^ In one specimen, it could not be determined whether FN was 66 or 67; the other three had 66.[78]
- ^ Reported as Oryzomys megacephalus by Musser et al. (1998), but only perenensis is currently recorded from Colombia.[87]
- ^ This species was described among others from specimens of "Oryzomys laticeps" from Rio Cobaría, Arauca Department[105] (actually in Boyacá Department);[106] San Juan Nepomuceno, Bolívar Department;[105] Socorre, upper Rio Sinu, Bolívar, Colombia;[107] and Cerro Azul, Panama.[104] "Oryzomys laticeps", as defined in the 1960s, included Transandinomys talamancae and no other species that occur in this region;[108] furthermore, Musser et al. (1998) listed Oryzomys talamancae for all these localities.[109]
References
- ^ a b Goldman, 1918, plate IV
- ^ . Retrieved 15 November 2021.
- ^ Musser et al., 1998, fig. 66; Linares, 1998, map 134
- ^ Allen, 1891, p. 193
- ^ Allen, 1899, p. 208
- ^ Allen, 1899, p. 209
- ^ Allen, 1899, p. 210
- ^ Thomas, 1900, p. 272
- ^ Thomas, 1901, p. 252
- ^ Robinson and Lyon, 1901, p. 142
- ^ Allen, 1908, p. 656
- ^ a b c d Weksler et al., 2006, p. 25
- ^ Musser et al., 1998, pp. 273–274
- ^ Allen, 1891, pp. 193–194
- ^ Allen, 1899, pp. 208–210; Musser et al., 1998, pp. 273–274
- ^ Thomas, 1900, pp. 272–273
- ^ Thomas, 1901, pp. 252–253
- ^ Robinson and Lyon, 1901, pp. 142–143
- ^ Allen, 1908, pp. 656–657
- ^ Goldman, 1918, pp. 71–74
- ^ Hershkovitz, 1960, p. 544; Musser et al., 1998, p. 179
- ^ Musser and Williams, 1985, p. 9
- ^ Musser and Williams, 1985, p. 7
- ^ Musser and Williams, 1985, pp. 13–14
- ^ Musser et al., 1998, pp. 275–276
- ^ Weksler, 2006, pp. 75–77
- ^ Weksler, 2006, figs. 34–39
- ^ Weksler et al., 2006, p. 26
- ^ Weksler, 2006, p. 3
- ^ Musser and Carleton, 2005
- ^ a b c d e f g Goldman, 1918, p. 73
- ^ a b Musser and Carleton, 2005, p. 1155
- ^ Musser and Williams, 1985, p. 14; Musser et al., 1998, p. 173
- ^ Musser et al., 1998, p. 125
- ^ Musser et al., 1998, p. 127
- ^ Musser et al., 1998, pp. 167, 169
- ^ a b c Musser et al., 1998, p. 169
- ^ Patton et al., 2000, p. 140
- ^ Musser and Williams, 1985, p. 18; Musser et al., 1998, p. 169
- ^ a b c d e f Musser and Williams, 1985, p. 14
- ^ Musser et al., 1998, pp. 127–128
- ^ a b Musser et al., 1998, pp. 128–129
- ^ a b c d e Musser et al., 1998, p. 173
- ^ a b Fleming, 1970, p. 479
- ^ a b Goldman, 1918, p. 71
- ^ Musser and Williams, 1985, table 2
- ^ a b c Musser et al., 1998, p. 129
- ^ a b Musser et al., 1998, p. 131
- ^ Goldman, 1918, pp. 71–72
- ^ Goldman, 1918, p. 72
- ^ Weksler et al., 2006, p. 25; Musser et al., 1998, p. 124
- ^ Linares, 1998, p. 287; Tirira, 2007, p. 200; Reid, 2009, p. 208
- ^ Weksler, 2006, pp. 17, 19
- ^ Steppan, 1995, table 5
- ^ Goldman, 1918, p. 73; Musser and Williams, 1985, p. 14
- ^ Weksler, 2006, pp. 31–32
- ^ Weksler, 2006, p. 29, table 5
- ^ a b Musser et al., 1998, p. 135
- ^ a b Musser et al., 1998, p. 174
- ^ Musser and Williams, 1985, p. 14; Weksler, 2006, pp. 34–35
- ^ Goldman, 1918, p. 73; Weksler, 2006, p. 35; Musser and Williams, 1985, p. 14
- ^ Weksler, 2006, pp. 38–39
- ^ a b Musser et al., 1998, p. 140
- ^ Weksler, 2006, p. 41
- ^ Weksler, 2006, p. 42
- ^ Weksler, 2006, p. 43
- ^ Weksler, 2006, pp. 43–44
- ^ Musser et al., 1998, pp. 140–141
- ^ Weksler, 2006, pp. 42–43
- ^ Goldman, 1918, plate V
- ^ Weksler, 2006, p. 55
- ^ Weksler, 2006, pp. 55–56
- ^ Weksler, 2006, pp. 56–57
- ^ Weksler, 2006, p. 58, footnote 10
- ^ Weksler, 2006, pp. 57–58; Voss and Linzey, 1981, p. 13
- ^ Goldman, 1918, plate VI
- ^ Musser et al., 1998, p. 163
- ^ Musser et al., 1998, pp. 163–164
- ^ Musser et al., 1998, pp. 164–165
- ^ a b Musser et al., 1998, p. 165
- ^ Musser et al., 1998, pp. 165–166
- ^ Musser et al., 1998, pp. 125, 169, table 13
- ^ Musser et al., 1998, p. 174; Patton et al., 2000, p. 140
- ^ a b Musser et al., 1998, p. 158
- ^ a b c d Musser et al., 1998, p. 157
- ^ Musser et al., 1998, pp. 157–158, footnote 9
- ^ Musser and Carleton, 2005, pp. 1151, 1153
- ^ Reid, 2009, p. 208; Tirira, 2007, p. 200
- ^ Fleming, 1970; 1971
- ^ Fleming, 1971, p. 5
- ^ Fleming, 1971, p. 60
- ^ Fleming, 1971, p. 50
- ^ Fleming, 1971, p. 22
- ^ Fleming, 1971, p. 23, fig. 6
- ^ a b c Linares, 1998, p. 288
- ^ Fleming, 1971, p. 40
- ^ Fleming, 1971, p. 65
- ^ Fleming, 1971, table 11
- ^ Fleming, 1971, p. 41
- ^ Fleming, 1971, p. 43
- ^ Fleming, 1971, p. 29
- ^ Fleming, 1971, p. 32
- ^ Fleming, 1971, p. 48
- ^ a b Lee and Strandtmann, 1967, p. 30
- ^ a b c Lee and Strandtmann, 1967, p. 28
- ^ Musser et al., 1998, p. 259
- ^ Lee and Strandtmann, 1967, p. 29
- ^ Hershkovitz, 1960, p. 544; see Musser et al. (1998) for review.
- ^ Musser et al., 1998, pp. 150 (locality 16), 151 (localities 52, 53), 153 (locality 68)
- ^ Tipton et al., 1966, p. 42
- ^ Clark, 1967
- ^ Brennan and Reed, 1979, p. 535
- ^ Brennan and Yunker, 1966, p. 262
- ^ Tipton and Méndez, 1966, p. 330
- ^ Durden and Musser, 1994, p. 30
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- Anderson, R.P.; Aguilera, M.; Gómez-Laverde, M.; Samudio, R.S. Jr.; Pino, J.L. (2017). "Transandinomys talamancae". IUCN Red List of Threatened Species. 2017: e.T15615A22332803. Retrieved 2 January 2020.
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- Musser, G.G., Carleton, M.D., Brothers, E.M. and Gardner, A.L. 1998. Systematic studies of oryzomyine rodents (Muridae: Sigmodontinae): diagnoses and distributions of species formerly assigned to Oryzomys "capito". Bulletin of the American Museum of Natural History 236:1–376.
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- Tipton, V.J., Altman, R.M. and Keenan, C.M. 1966. Mites of the subfamily Laelaptinae in Panama (Acarina: Laelaptidae). pp. 23–82 in Wenzel, R.L. and Tipton, V.J. (eds.). Ectoparasites of Panama. Chicago: Field Museum of Natural History.
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External links
- Media related to Oryzomys talamancae at Wikimedia Commons
- Data related to Transandinomys talamancae at Wikispecies