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Dipsas vagrans (DUNN, 1923)

IUCN Red List - Dipsas vagrans - Least Concern, LC

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Higher TaxaColubridae (Dipsadinae), Colubroidea, Caenophidia, Alethinophidia, Serpentes, Squamata (snakes)
Subspecies 
Common NamesE: Dunn's Tree Snake 
SynonymPseudopareas vagrans DUNN 1923: 187
Pseudopareas vagrans — MARX 1958
Sibynomorphus vagrans — PETERS 1960: 161
Sibynomorphus vagrans — CADLE 2007: 233
Sibynomorphus vagrans — WALLACH et al. 2014: 671
Dipsas vagrans — ARTEAGA et al. 2018 
DistributionPeru (Cajamarca)

Type locality: Bellavista, Peru  
Reproductionoviparous 
TypesHolotype: MCZ 17284, adult female 
DiagnosisDiagnosis: Sibynomorphus vagrans is a brownish or grayish snake with a variable number (5–10) of broad dark crossbands anteriorly, much wider than the interspaces, and a posterior pattern consisting of an obscure network-like pattern, irregular flecks, or narrow, somewhat indistinct, irregular crossbands (much narrower than interspaces) (Fig. 28). The venter is unmarked (most specimens) or has a few dark spots that never form dense arrays. This species has a relatively low number of ventrals (149–155 in males, 154–159 in females) and relatively high number of subcaudals (80–87 in males, 72–79 in females). The top of the head is ornately patterned and the nape has a narrow pale collar with a characteristic obtuse angular shape.
Sibynomorphus vagrans is distinguished from all other species of the genus in northern South America by its combination of relatively low ventral counts and high subcaudal counts (Table 1). Sibynomorphus vagus is similar to S. vagrans in ventral counts but lacks well-defined crossbands anteriorly (and they are narrower than interspaces when present), lacks a pale nape collar, and has fewer subcaudals (60–65 in males, 56–60 in females). In addition, S. vagrans has a longer tail on average (25–29% of total length in males, 23–26% of total length in females) than S. vagus (23–24% in males, 20–21% in females).
Distinct broad anterior crossbands similar to those of S. vagrans are found only in S. oligozonatus and S. williamsi. Sibynomorphus oligozonatus differs from S. vagrans in having a foreshortened snout (compare Fig. 4 and Figs. 30, 31), fewer subcaudals, and fewer supralabials (6–7 vs. 8–9 in S. vagrans). Sibynomorphus williamsi differs from S. vagrans in having 6 supralabials (3–4 touching the eye) compared with 8 (usually) with 4–5 touching the eye in S. vagrans, higher ventral counts (173–188), lower subcaudal counts (56–73), and in S. williamsi, the dorsal crossbands are distinct virtually the entire length of the body (sometimes dorsal saddles and alternating lateral blotches posteriorly). Sibynomorphus oneilli differs from S. vagrans in having more ventrals (≥152 in males, ≥160 in females), fewer subcaudals (62–77 in males, 57–64 in females), a shorter tail (22–26% of total length in males, 20–22% in females), a less ornately patterned head, narrower anterior dorsal crossbands, and a venter heavily marked with bold black spots. Sibynomorphus petersi differs from S. vagrans in having more ventrals (>160), a primarily brown dorsum with narrower crossbands (when present), interspaces brown (compared with whitish in S. vagrans), and a venter densely patterned with dark brown markings. (Cadle 2007)


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CommentSibynomorphus vagrans is known only from the type series (n=27) collected by G. K. Noble, fide Cadle 2007.

Diet: primarily molluscs (T. de Lema, pers. comm., 16 Oct 2015).

Distribution: See map in Cadle 2007: 229 (Fig. 25)

Habitat: fully arboreal (Harrington et al. 2018). 
EtymologyDunn (1923: 187) did not elaborate on the meaning of his species epithet, saying only that Sibynomorphus vagrans was ‘‘a species closely allied to [S. vagus] but quite distinct.’’ To reflect his supposition that the two species were closely related, Dunn might have used the name vagrans (originally of Anglo-French and Germanic origin) because it is a latinized cognate associated with the Latin word vagus (meaning wandering or roaming or indefinite; from vagor, to wander). However, the color pattern of S. vagrans bears little resemblance to that of S. vagus. 
References
  • Arteaga A, Salazar-Valenzuela D, Mebert K, Peñafiel N, Aguiar G, Sánchez-Nivicela JC, Pyron RA, Colston TJ, Cisneros-Heredia DF, Yánez-Muñoz MH, Venegas PJ, Guayasamin JM, Torres-Carvajal O 2018. Systematics of South American snail-eating snakes (Serpentes, Dipsadini), with the description of five new species from Ecuador and Peru. ZooKeys 766: 79-147 - get paper here
  • Cadle, J.E. 2007. The snake genus Sibynomorphus (Colubridae: Dipsadinae: Dipsadini) in Peru and Ecuador, with comments on the systematics of Dipsadini. Bull. Mus. Comp. Zool. Harvard 158(5):183-283 - get paper here
  • Dunn, E. R. 1923. Some snakes from North Western Peru. Proc. Biol. Soc. Washington 36: 185-188 - get paper here
  • 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
  • KOCH, CLAUDIA; PABLO J. VENEGAS, ROY SANTA CRUZ, WOLFGANG BÖHME 2018. Annotated checklist and key to the species of amphibians and reptiles inhabiting the northern Peruvian dry forest along the Andean valley of the Marañón River and its tributaries. Zootaxa 4385 (1): 001–101 - get paper here
  • Marx,H. 1958. Catalogue of type specimens of reptiles and amphibians in Chicago Natural History Museum. Fieldiana Zool. 36: 407-496 - 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
  • 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.
 
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