MarketHammond's rice rat
Company Profile

Hammond's rice rat

Mindomys hammondi, also known as Hammond's rice rat or Hammond's oryzomys, is an endangered species of rodent in the tribe Oryzomyini of family Cricetidae. Formerly considered to be related with Nectomys, Sigmodontomys, Megalomys, or Oryzomys, it is now placed in then genus Mindomys, but its relationships remain obscure; some evidence supports a placement near Oecomys or as a basal member of Oryzomyini.

Taxonomy
Discovery and classification in Nectomys In 1913, Oldfield Thomas of the British Museum of Natural History (BMNH) in London published the first description of Mindomys hammondi, using two specimens collected at Mindo in Pichincha Province, Ecuador, in the same year by Gilbert Hammond. He named the species Nectomys hammondi, classifying it in the genus Nectomys, which at the time included not only the large water rats currently placed in it, but also Sigmodontomys alfari and Oryzomys dimidiatus. He considered the animal to be most closely related to Nectomys russulus, a species he had himself described in 1897 and which is now recognized as a synonym of Sigmodontomys alfari. In his 1941 review The Families and Genera of Living Rodents, Sir John Ellerman retained N. hammondi as a species of Nectomys, but noted that the features of its teeth were atypical for the genus, as "the cusps appear to show no tendency to become suppressed." Reviewing the genus Nectomys in 1944, Philip Hershkovitz listed N. hammondi among species of Nectomys incertae sedis (of uncertain position), and considered its placement in Nectomys as dubious. Characters he listed as conflicting with a Nectomys identity of the species included the short hindfoot with a long fifth toe, the weakly developed posterolateral palatal pits (perforations of the palate near the third molars), and the orientation of the zygomatic plate. Classification in Oryzomys Hershkovitz published again on Nectomys in 1948 after examining additional material, including the holotype of N. hammondi. He now considered the latter to be a species of Oryzomys (at the time a large genus that included most of the current members of the tribe Oryzomyini), but distinctive enough to be placed in its own subgenus. Noting that the species was "extremely long-tailed", he introduced the subgeneric name Macruroryzomys for hammondi. In 1970, Hershkovitz treated the species in another publication and noted that his name Macruroryzomys was a nomen nudum ("naked name") because he had not explicitly mentioned characters differentiating it from other taxa in his 1948 publication. Nevertheless, he did not do anything to rectify the situation, and Macruroryzomys remains a nomen nudum. Hershkovitz rejected any relationship between O. hammondi and Nectomys or O. aphrastus and instead argued that O. hammondi was closely similar to Megalomys and may be close to the ancestor of Megalomys. In 1982, Steadman and Ray mentioned the animal in passing under the name Macruroryzomys hammondi and reaffirmed its relationship to Megalomys. In the 2005 third edition of Mammal Species of the World, Guy Musser and Michael Carleton listed O. hammondi as an Oryzomys of obscure affinities, but suggested that it may be related to Megalomys. Traits of O. hammondi that supported the latter placement include: a relatively short palate that does not extend behind the maxillary bones; simple posterolateral palatal pits; absence of a capsular process (a raising of the bone of the mandible, or lower jaw, at the back end of the incisor); and presence of the posteroloph on the upper third molar (a crest at the back of the tooth). In these characters, O. hammondi differs from many or most Oryzomyini and is similar to some species outside Oryzomyini, but all traits of O. hammondi are present in at least one other member of the tribe. Traits shared by O. hammondi and Oecomys included: tail with the same coloration above and below (unicolored); parietal bones extending to the sides of the skull; narrow zygomatic plate, without a zygomatic notch; posteroloph present on upper third molar; mesoflexus (a valley in the molar crown in front of the mesoloph crest) on upper second molar not divided in two. In Weksler's analysis, species placed in Oryzomys did not form a coherent (monophyletic) group, but instead were found at various positions across the oryzomyine tree, and he suggested that most of these species, including O. hammondi, should be placed in new genera. Later in 2006, Weksler and others described ten new genera for species formerly placed in Oryzomys, including Mindomys for hammondi. Noting its "enigmatic distribution" and uncertain but perhaps basal position within Oryzomyini, they labeled the species an "extraordinary rat" worthy of continued inquiry. ==Description==
Description
Mindomys hammondi is a large rice rat; all other rats known within its range are smaller. The fur is relatively short and woolly and is buffy with a grayish tone above and much paler—yellow or white—below, with the bases of the hairs grey. It has a long snout and small, dark ears that appear hairless. The vibrissae (whiskers) are long. The very long tail is dark both above and below The fifth digit reaches to about half the length of the second phalange of the fourth. In specimens with published measurements, head and body length is , tail length is , hindfoot length is , ear length is , and greatest length of skull is . Skull In the skull, the rostrum (front part) is large and robust. The zygomatic plate is narrow and lacks a zygomatic notch, an extension of the plate at the front. The plate's back margin is level with the front of the first upper molar. The narrowest part of the interorbital region, located between the eyes, is to the front and its margins exhibit strong beading. Various crests develop on the long braincase, especially in old animals. The incisive foramina, perforations of the palate between the incisors and the molars, are short, not extending between the molars. The condition of the posterolateral palatal pits is variable, with some individuals having small pits and others having larger pits that may be recessed into a fossa (depression). The palate is moderately long, extending beyond the molars but not beyond the posterior margins of the maxillary bone. In most specimens, the roof of the mesopterygoid fossa, the gap behind the back of the palate, is not perforated by sphenopalatine vacuities and thus it is fully ossified; if present, these vacuities are small. Mindomys lacks an alisphenoid strut; in some other oryzomyines, this extension of the alisphenoid bone separates two openings (foramina) in the skull, the masticatory–buccinator foramen and the foramen ovale accessorium. There are no openings in the mastoid bone. The squamosal bone lacks a suspensory process that contacts the tegmen tympani, the roof of the tympanic cavity, a defining character of oryzomyines. In the mandible, the mental foramen, an opening in the mandible just before the first molar, opens to the outside, not upwards as in a few other oryzomyines. The upper and lower masseteric ridges, which anchor some of the chewing muscles, join at a point below the first molar and do not extend forward beyond that point. Molars The molars are bunodont (with the cusps higher than the connecting crests) and brachydont (low-crowned). On the upper first and second molar, the outer and inner valleys between the cusps and crests interpenetrate. Many accessory crests are present, including the mesolophs and mesolophids. The anterocone and anteroconid, the front cusps on the upper and lower first molar, are not divided into smaller outer and inner cusps. so that each of the three upper molars has two roots on the outer side and one on the inner side and each of the lower molars has one root at the front and one at the back. ==Distribution and ecology==
Distribution and ecology
A rare species, Mindomys hammondi is known only from Ecuador. Between 1913 and 1980, eight specimens were collected at Mindo, a "tiny agricultural community" There are two other locations named "Concepción" in northwestern Ecuador, and Diego Tirira suggested in 2007 that the specimen may instead be from one of these. Another specimen is known from Chaco, Imbabura Province, at an altitude of . Almost nothing is known of the biology of Mindomys. in 2007, Tirira agreed, citing the animal's broad feet. Tirira also suggested that it is nocturnal (active during the night) and solitary and eats fruits, seeds, and insects. According to the 2009 IUCN Red List, it lives on the ground and "apparently has some affinity with water". ==Conservation status==
Conservation status
The IUCN Red List lists Mindomys hammondi as "endangered" in view of its small known distribution and a continuing decline in the extent and quality of its habitat. Up to 40% of its habitat may already have been destroyed, and the species was last recorded in 1980. It is not known to occur in any protected areas, but has been recorded close to the protected forest of Mindo-Nambillo. It prefers well-conserved primary forest. ==Notes==
Literature cited
• Eisenberg, J.F. and Redford, K.H. 1999. Mammals of the Neotropics. Volume 3, The central Neotropics: Ecuador, Peru, Bolivia, Brazil. University of Chicago Press, 624 pp.  • Ellerman, J.R. 1941. The families and genera of living rodents. Vol. 2. Family Muridae. London: British Museum of Natural History, 690 pp. • Hershkovitz, P. 1944. "A systematic review of the Neotropical water rats of the genus Nectomys". Miscellaneous Publications of the Museum of Zoology, University of Michigan 58:1–88. • Hershkovitz, P. 1948. "Mammals of northern Colombia. Preliminary report No. 3: Water rats (genus Nectomys), with supplemental notes on related forms". Proceedings of the United States National Museum 98:49–56. • Hershkovitz, P. 1970. "Supplementary notes on Neotropical Oryzomys dimidiatus and Oryzomys hammondi (Cricetinae)" (subscription required). Journal of Mammalogy 51(4):789–794. • McCain, C.M., Timm, R.M. and Weksler, M. 2007. "Redescription of the enigmatic long-tailed rat Sigmodontomys aphrastus (Cricetidae: Sigmodontinae) with comments on taxonomy and natural history" (subscription required). Proceedings of the Biological Society of Washington 120:117–136. • • Percequillo, A.R., Weksler, M. and Costa, L.P. 2011. "A new genus and species of rodent from the Brazilian Atlantic Forest (Rodentia: Cricetidae: Sigmodontinae: Oryzomyini), with comments on oryzomyine biogeography" (subscription required). Zoological Journal of the Linnean Society 161(2):357–390. • Ray, C.E. 1962. "The Oryzomyine Rodents of the Antillean Subregion". Doctor of Philosophy thesis, Harvard University, 211 pp. • Steadman, D.W. and Ray, C.E. 1982. "The relationships of Megaoryzomys curioi, an extinct cricetine rodent (Muroidea: Muridae) from the Galápagos Islands, Ecuador". Smithsonian Contributions to Paleobiology 51:1–23. • Thomas, O. 1913. "New mammals from South America". Annals and Magazine of Natural History (8)12:566–574. • Tirira, D. 2007. "Guia de campo de los mamíferos del Ecuador". Quito: Ediciones Murciélago Blanco, publicación especial sobre los mamíferos del Ecuador 6, 576 pp. (in Spanish). • • Weksler, M. 2006. "Phylogenetic relationships of oryzomyine rodents (Muroidea: Sigmodontinae): separate and combined analyses of morphological and molecular data". Bulletin of the American Museum of Natural History 296:1–149. • Weksler, M., Percequillo, A.R. and Voss, R.S. 2006. "Ten new genera of oryzomyine rodents (Cricetidae: Sigmodontinae)". American Museum Novitates 3537:1–29.
tickerdossier.comtickerdossier.substack.com