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Dendrophidion apharocybe CADLE, 2012

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Higher TaxaColubridae, Colubrinae, Colubroidea, Caenophidia, Alethinophidia, Serpentes, Squamata (snakes)
Subspecies 
Common Names 
SynonymDendrophidion apharocybe CADLE 2012
Dendrophidion dendrophis — GAIGE et al 1937: 12 (part)
Dendrophidion vinitor — SMITH 1941: 74–75 (part)
Dendrophidion apharocybe — WALLACH et al. 2014: 224
Dendrophidion apharocybe — SUNYER & MARTÍNEZ-FONSECA 2023 
DistributionCosta Rica, Honduras, Nicaragua, Panama

Type locality: Finca La Selva, 40 m elevation, Heredia Province, Costa Rica  
Reproductionoviparous (not imputed, fide Zimin et al. 2022) 
TypesHolotype: LACM 148593, an adult male. Collected 9 December 1974 by C. Dock, Carl Lieb, and Catherine Toft. The holotype is 908 mm total length; 574 mm SVL; 334 mm tail length (complete); (Figs. 2B, 7, 14C). Paratypes: USNM 
DiagnosisDiagnosis: Dendrophidion apharocybe is characterized by (1) dorsocaudal reduction from 8 to 6 occurring posterior to subcaudal 25 (range, 26–63); (2) single anal plate; (3) relatively low subcaudal counts (<130 in males and females); (4) black-edged pale crossbands on the neck nearly always more than one scale row wide; (5) immaculate ventrals and subcaudals except for lateral dark pigment; (6) a relatively short hemipenis with a bulbous apex strongly inclined toward the sulcate side (asulcate edge of apex higher than sulcate edge) and largely devoid of ornamentation (apex nude). The combination of few subcaudals and a single anal plate will distinguish D. apharocybe from all other species of Dendrophidion except D. vinitor, D. crybelum, and D. paucicarinatum.
Dendrophidion apharocybe differs from species of the D. percarinatum group (D. bivittatum, D. brunneum, D. paucicarinatum,D.percarinatum)in having the dorsocaudal reduction from 8 to 6 usually posterior to subcaudal 30 (26–30 in some specimens from Costa Rica and Panama; see Sexual Dimorphism and Geographic Trends). A single anal plate will distinguish D. apharocybe from all of these except some individuals of D. paucicarinatum (anal plate variable in this species). Dendrophidion paucicarinatum usually has a more uniformly colored dorsum lacking distinct crossbands, has narrow dark lines across the venter in adults and many juveniles, has a higher number of ventrals (>175 compared with <170 in D. apharocybe), and has more weakly keeled dorsal scales. Dendrophidion apharocybe differs from D. boshelli in having 17 midbody scale rows (15 in D. boshelli). Dendrophidion apharocybe has fewer subcaudals (<130) and usually a shorter adult relative tail length (<60% of SVL) than D. nuchale auctorum and D. dendrophis (>130 and usually >60% of SVL, respectively); the anal plate may be either single or divided in these last two species, and their venters are often heavily marked with dark pigment (immaculate in D. apharocybe) (CADLE 2012: 200). 
CommentSimilar species: Dendrophidion apharocybe previously has been confused with another new species, D. crybelum, and with D. vinitor as redefined by CADLE 2012.

Distribution: map in CADLE 2012: 206.

Habitat: partly arboreal (Harrington et al. 2018).

Similar species: D. crybelum, D. vinitor. 
EtymologyNamed after the Greek words aphares (άϕαρής), meaning naked or unclad, and kybe (кύβη), meaning head. The ‘‘naked head’’ refers to the distinctive unadorned apex of the hemipenis of D. apharocybe compared with its sibling species. The species name is a feminine noun in apposition. 
References
  • Cadle, John E. 2012. Cryptic Species Within the Dendrophidion vinitor Complex In Middle America (Serpentes: Colubridae). Bull. Mus. Comp. Zool. Harvard 160 (4): 183-240. - get paper here
  • Fuentes, Rogemif; Aschcroft, Jesse; Erick Barría, Helio Quintero-Arrieta, Alexis Baules, Abel Batista, Eduardo Zambrano, Marcos Ponce 2023. Herpetological diversity in forests of Portobelo National Park, Colón Biological Corridor, Panama. Reptiles & Amphibians 30 (1): e18434 - 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
  • Hilje B, Chaves G, Klank J, Timmerman F, Feltham J, Gillingwater S, Piraino T, Rojas E 2020. Amphibians and Reptiles of the Tirimbina Biological Reserve: a baseline for conservation, research and environmental education in a lowland tropical wet forest in Costa Rica. Check List 16(6): 1633-1655 - get paper here
  • McCranie, James R. 2015. A checklist of the amphibians and reptiles of Honduras, with additions, comments on taxonomy, some recent taxonomic decisions, and areas of further studies needed. Zootaxa 3931 (3): 352–386 - get paper here
  • Morato, Sérgio Augusto Abrahão; Guilherme Nunes Ferreira; Michela Rossane Cavilha Scupino (eds.) 2018. Herpetofauna da Amazônia Central: Estudos na FLONA de Saracá-Taquera. Curitiba, Pr: STCP Engenharia de Projetos Ltda.; Porto Trombetas, Pa: MRN – Mineração Rio do Norte S.A., 2018.<br />210p. - get paper here
  • Ray, Julie M. and Patty Ruback 2015. Updated checklists of snakes for the provinces of Panamá and Panamá Oeste, Republic of Panama. Mesoamerican Herpetology 2 (2): 168-188 - get paper here
  • Solís, J. M., L. D. Wilson, and J. H. Townsend. 2014. An updated list of the amphibians and reptiles of Honduras, with comments on their nomenclature. Mesoamerican Herpetology 1: 123–144 - get paper here
  • Sunyer, Javier 2014. An updated checklist of the amphibians and reptiles of Nicaragua. Mesoamerican Herpetology 1 (2): 186–202. - get paper here
  • Sunyer, Javier & José́ Gabriel Martínez-Fonseca 2023. An updated country checklist to the amphibians and reptiles of Nicaragua. REVISTA NICARAGÜENSE DE BIODIVERSIDAD (100): 1-25 - 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.
  • Zimin, A., Zimin, S. V., Shine, R., Avila, L., Bauer, A., Böhm, M., Brown, R., Barki, G., de Oliveira Caetano, G. H., Castro Herrera, F., Chapple, D. G., Chirio, L., Colli, G. R., Doan, T. M., Glaw, F., Grismer, L. L., Itescu, Y., Kraus, F., LeBreton 2022. A global analysis of viviparity in squamates highlights its prevalence in cold climates. Global Ecology and Biogeography, 00, 1–16 - get paper here
 
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