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Dipsas brevifacies (COPE, 1866)

IUCN Red List - Dipsas brevifacies - Least Concern, LC

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Higher TaxaColubridae (Dipsadinae), Colubroidea, Caenophidia, Alethinophidia, Serpentes, Squamata (snakes)
Subspecies 
Common NamesE: Short-faced snail eater, Snail-eating Thirst Snake
S: Caracolera de Cara Corta 
SynonymTropidodipsas brevifacies COPE 1866: 127
Dipsadomorus fasciatus BOCOURT 1884: 135
Leptognathus torquatus COPE 1885: 172 (substitute name for D. fasciatus)
Dirosema brevifacies — BOCOURT 1908 (fide VILLA et al. 1988)
Leptognathus brevifacies — WERNER 1910: 280
Sibynomorphus brevifacies — SCHMIDT & ANDREWS 1936 (fide VILLA et al.)
Dipsas brevifacies — PETERS 1960: 38
Dipsas brevifacies — PETERS & OREJAS-MIRANDA 1970: 86
Dipsas brevifacies — VILLA et al. 1988
Dipsas brevifacies — LINER 1994
Dipsas brevifacies — CAMPBELL 1998
Dipsas brevifacies — LINER 2007
Dipsas brevifacies — WALLACH et al. 2014: 231 
DistributionMexico (Yucatan, Campeche, Quintana Roo), Belize [HR 17: 67], Guatemala

Type locality: Yucatán.  
Reproductionoviparous 
TypesHolotype: USNM 24886, male. 
DiagnosisDESCRIPTION (apparently based on ~23 specimens). Rostral broader than deep, barely visible from above; internasals three-fourths the length of prefrontals; frontal as long as or slightly shorter than broad; nasal divided; loreal enters orbit; preoculars none, 1, 2 or 3 (loreal and preocular region extremely variable, see below); postoculars 3; suboculars none or 1; primary temporals 2, secondary temporals 3, tertiary temporals 4; upper labials 9, 4th and 5th entering orbit. Lower labials 9 to 13, the first 2 pairs in contact behind mental, 4 labials in contact with first chin shield; no lower labial enlarged; 2 pairs of chin shields.
Ventrals 167-176 in males, 166-174 in females; anal entire; subcaudals 83-100 in males, 69-87 in females. Dorsal scale rows 15 from 5th to 7th ventral to anus; vertebral row not to scarcely enlarged; caudodorsals:
Males: 6 2+3 (19-31) 4 1+2 (51-82) 2 (83-100)
Females: 6 2+3 (11-24) 4 1+2 (48-63) 2 (69-87)

Maxillary teeth 17-19 (9 individuals); palatine teeth 11-16 (7); pterygoid teeth 3-6 (9).

Body length, male 373 mm., female 357 mm., minimum 131 mm.; tail length, male 155 mm., female 123 mm., minimum 42 mm.

Coloration: Dorsal ground color cream to white, occasionally with pink cast, with, in males, 12-16 complete dark-brown to black rings on body, 6-11 on tail, in females, 10-14 on body, 5-8 on tail; which are longer anteriorly (15 to 20 scale rows) than posteriorly (8-12 scale rows), and shorter ventrally than dorsally by one or two scales; eight interspaces, 2 to 5 scale rows wide at vertebral row, wider ventrally when black ring is narrowed; both rings and interspaces unicolor, without lighter centers or spotting and stippling (Pl. Ia). Belly as in dorsum; dorsal bands meet uniformly on midventral line on body, may be irregular on tail, with edges widely separated.
Head unicolor black from tip of snout to posterior edge of parietals and to primary or secondary temporal rows; followed by a nuchal collar which is cream-colored a s are the rest of interspaces. Chin black to end of paired chin shields or to first unpaired gulars, edges usually confluent with the black of head.

Juvenile pattern as in adult.

Schmidt and Andrews (1936:175) stated that “In life the light body-bands were bittersweet pink alternating with black, with a flame scarlet neck-band.” (Peters 1960: 39).

Variation: see Fig. 5 in Peters 1960: 41 for variation in head scalation. 
CommentHabitat: fully arboreal (Harrington et al. 2018). 
References
  • Aguilar-López JL, Luría-Manzano R, Pineda E, Canseco-Márquez L 2021. Selva Zoque, Mexico: an important Mesoamerican tropical region for reptile species diversity and conservation. ZooKeys 1054: 127-153 - get paper here
  • Bocourt,M.F. 1884. Note sur quelques ophidiens nouveaux, provenant de l'Amerique inter-tropicale. Bull. Soc. Philomath. Paris (7) 8: 133-142 - get paper here
  • Calderon, R.; Cedeño-Vázquez, J.R. & Pozo, C. 2003. New distributional records for amphibians and reptiles from Campeche, Mexico. Herpetological Review 34 (3): 269-272 - get paper here
  • Campbell, J.A. 1998. Amphibians and reptiles of northern Guatemala, the Yucatán, and Belize. Norman: University of Oklahoma Press, xiii + 380 pp. - get paper here
  • Colston, Timothy J.; José António L. Barão-Nóbrega, Ryan Manders, Alice Lett, Jamie Wilmott, Gavin Cameron, Sidony Hunter, Adam Radage, Etienne Littlefair, Robert J. Williams, Antonio Lopez Cen, Kathy Slater 2015. Amphibians and reptiles of the Calakmul Biosphere Reserve, México, with new records. Check List 11 (5): 1759 - get paper here
  • Cope, E.D. 1866. Fourth contribution lo the herpetology of tropical America. Proc. Acad. nat. Sci. Philadelphia, 18: 123-132 - get paper here
  • Cope, E.D. 1885. Twelfth contribution to the herpetology of tropical America. Proc. Amer. Philos. Soc. 22: 167-194 [1884] - get paper here
  • Dundee, H. A., WHITE, D. A., & RICO GRAY,V. 1986. Observations on the distribution and biology of some Yucatán Peninsula amphibians and reptiles. Bull. Maryland Herp. Soc. 22 (2): 37-50 - get paper here
  • Gaige,H. 1936. Some reptiles and amphibians from Yucatan and Campeche, Mexico. Carnegie Inst. Wash. Publ., (457): 289-304.
  • Harrington, Sean M; Jordyn M de Haan, Lindsey Shapiro, Sara Ruane 2018. Habits and characteristics of arboreal snakes worldwide: arboreality constrains body size but does not affect lineage diversification. Biological Journal of the Linnean Society 125 (1): 61–71 - get paper here
  • Harvey, Michael B. and Dirk Embert 2008. Review of Bolivian Dipsas (Serpentes: Colubridae), with Comments on Other South American Species. Herpetological Monographs 22 (1): 54-105 - get paper here
  • Heimes, P. 2016. Snakes of Mexico. Chimaira, Frankfurt, 572 pp
  • Kofron, C.P. 1982. A review of the Mexican snail-eating snakes, Dipsas brevifacies and Dipsas gaigeae. Journal of Herpetology 16 (3): 270-286 - get paper here
  • Köhler, G. 2008. Reptiles of Central America. 2nd Ed. Herpeton-Verlag, 400 pp.
  • Köhler, Gunther, J. Rogelio Cedeño-Vázquez, Till Kirstein and Pablo Beutelspacher-García. 2016. The Chetumal Snake Census: generating biological data from road-killed snakes. Part 2. Dipsas brevifacies, Sibon sanniolus, and Tropidodipsas sartorii. Mesoamerican Herpetology 3 (3): 689–705 - get paper here
  • Lee, J. C. 2000. A field guide to the amphibians and reptiles of the Maya world. Cornell University Press, Ithaca,
  • Lee, J.C. 1996. The amphibians and reptiles of the Yucatán Peninsula. Comstock, Cornell University Press, Ithaca, 500 pp.
  • Liner, Ernest A. 2007. A CHECKLIST OF THE AMPHIBIANS AND REPTILES OF MEXICO. Louisiana State University Occasional Papers of the Museum of Natural Science 80: 1-60 - get paper here
  • Nahuat-Cervera, Pedro Enrique 2020. Amphibians and reptiles of the Hobonil Educative Center, Tzucacab, Yucatán, Mexico. Rev. Latinoamer. Herp. 3 (1): 53-65 - get paper here
  • Ortiz-Medina, J. A., Cabrera-Cen , D. I., Nahuat-Cervera, P. E. and Chable-Santos, J. B. 2020. New distributional records for the herpetofauna of Campeche and Yucatan, Mexico. Herpetological Review 51: 83-87. - get paper here
  • O’Shea, M. 2018. The Book of Snakes. Ivy Press / Quarto Publishing, London, - get paper here
  • Peters , J. A. 1960. The snakes of the subfamily Dipsadinae. Misc. Publ. Mus. Zool., Univ. Michigan (114): 224 pp. - get paper here
  • Schmidt, K. P, & ANDREWS, E. W. 1936. Notes on snakes from Yucatán. Field Mus. Nat Hist. Zool. Ser. 20: 167-187. - get paper here
  • Wallach, Van; Kenneth L. Williams , Jeff Boundy 2014. Snakes of the World: A Catalogue of Living and Extinct Species. [type catalogue] Taylor and Francis, CRC Press, 1237 pp.
  • Werner, F. 1910. Neue oder seltenere Reptilien des Musée Royal d'Histoire Naturelle de Belgique in Brüssel. [Mabuia dolloi, Mabuia polylepis]. Zool. Jb. Abt. Syst. Okol. Geogr. 28 [1909]: 263-288. - get paper here
 
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