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Bothriechis guifarroi TOWNSEND, MEDINA-FLORES, WILSON, JADIN & AUSTIN, 2013

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Higher TaxaViperidae, Crotalinae, Colubroidea, Caenophidia, Alethinophidia, Serpentes, Squamata (snakes)
Subspecies 
Common Names 
SynonymBothriechis guifarroi TOWNSEND, MEDINA-FLORES, WILSON, JADIN & AUSTIN 2013
Bothrops nigroviridis — MEYER 1969: 420 (part.)
Bothriechis marchi — CAMPBELL 1982: 381 (part.)
Bothrops marchii — WILSON & MEYER 1985: 120 (part.)
Bothriechis guifarroi — MASON et al. 2019 
DistributionHonduras (Atlántida), elevation 1,015–1,450 m

Type locality: La Liberacíon (Fig. 4A,C), 15.5302°N, 87.2939°W (DD), 1,015 m elevation, Refugio de Vida Silvestre Texíguat, Departamento de Atlántida, Honduras  
Reproductionviviparous (not imputed, fide Zimin et al. 2022) 
TypesHolotype: UTA R-60303 (Figs 2, 3), an adult male, collected 25 July 2010 by the field team of E. Aguilar, A. Contreras, L. Gray, L.A. Herrera-B., M. Medina-Flores, A. Portillo, A. Stubbs, and J. H. Townsend. Original field number JHT 3243. Genbank accession numbers: 16S (KC847259), cyt b (KC847275). Paratypes (8): HONDURAS: Departamento de Atlántida: Refugio de Vida Sil- vestre Texíguat: adult female (USNM 579875) collected 19 June 2010, two adult females (USNM 579876–77) collected 29 July 2010, and two unsexed neonates collected 18 June 2010 (USNM 579873–74), all from Cerro El Chino (Fig. 4B), 15.5225°N, 87.2802°W (DD), 1,360–1,450 m elevation, southeast of La Liberación. Two males (CM 156870 and MVZ 269305) collected 28 July 2010 from a ridge-top trail above La Liberación, 15.5418°N, 87.2891°W (DD), 1,290 m elevation. One male (USNM 579878) collected 30 July 2010 from La Liberación (Fig. 4A, C), 15.5302°N, 87.2939°W (DD), 1,015 m elevation. 
DiagnosisDiagnosis: Bothriechis guifarroi can be distinguished from the other members of the genus Bothriechis as follows (B. guifarroi features indicated first, those for species compared next): B. aurifer (distributed at moderate and intermediate elevations from extreme east-central Chiapas, Mexico, to east-central Guatemala) — adult color pattern (green vs. black-bordered yellow blotches on green background and prominent black postocular stripe) and juvenile color pattern (green with pale blue blotches or brown with pale paraventral stripe and dark dorsal blotches vs. pale lime green with black-bordered yellow blotches); B. bicolor (occurring marginally at low upward to intermediate elevations from southeastern Chiapas, Mexico, to south-central Guatemala) — number of dorsal scales at midbody (19 vs. 21) and condition of prelacunal and second supralabial scales (fused vs. separate); B. lateralis (moderate to marginally high elevations from northwestern Costa Rica to western Panama) — number of dorsal scale rows at midbody (19 vs. modal number of 23), adult color pattern (green vs. green with pale paravertebral bars and paraventral stripe), and juvenile color pattern (bi-morph pattern of green with blue dorsal blotching or brown with pale paraventral stripe and short unicolor dark blotches vs. uni-morph pattern of brown ground color with pale paraventral stripe and short bicolor dark and pale blotches); B. marchi (found marginally at low elevations up to intermediate elevations in northwestern Honduras and adjacent Guatemala) — condition of prelacunal and second supralabial scales (fused vs. separate), number of subcaudals in females (60–63 vs. 46–57); B. nigroviridis (moderate to intermediate elevations from north-central Costa Rica to west-central Panama) — adult color pattern (patternless green vs. green with very heavy black mottling), juvenile color pattern (green with pale blue blotches or brown with pale paraventral stripe and a series of short darker dorsal blotches vs. green with heavy black mottling), iris color (pale green, pale gray, or pale tan vs. almost black), numbers of ventral scales in both sexes (162–166 and 158–166 vs. 143–158 and 134–158), numbers of subcaudal in both sexes (60–68 and 60–63 vs. 49–56 and 44–58), and condition of prelacunal and second supralabial scales (fused vs. separate); B. rowleyi (moderate to intermediate elevations from extreme southeastern Oaxaca to northwestern Chiapas, Mexico) — condition of prelacunal and second supralabial scales (fused vs. almost always separate), iris color (pale green, pale gray, or pale tan vs. yellow), and juvenile color pattern (green with pale blue blotches or brown with pale paraventral stripe and a series of short darker dorsal blotches vs. pale yellowish green with brown or purple dorsal blotches); B. schlegelii (low to intermediate elevations from northwestern Chiapas, Mexico, southward through Central America and into northwestern South America as far as extreme western Venezuela and extreme northern Peru) — lack of superciliary scales in the former and their presence in the latter, number of suprala- bials (10–12, usually 10 vs. 7–10, usually 8), number of midbody dorsal scale rows (19 vs. 21–25, usually 23), and adult color pattern (green vs. extremely variable color and pattern involving ground color of yellow, pink, brown, gray, or green and dorsal blotching of a sizable array of colors, but sometimes absent; contrasting postocular stripe absent vs. present); B. supraciliaris (moderate to intermediate elevations from southwestern Costa Rica to west-central Panama) — lack of superciliary scales in the former and their presence in the latter, number of midbody dorsal scale rows (19 vs. 21–23, usually 23), number of ventral scales in both sexes (162–166 and 158–166 vs. 145–150 and 141–148), number of subcaudal scales in both sexes (60–68 and 60–63 vs. 48–54 and 45–52), and adult color pattern (green vs. extremely variable color and pattern involving ground color of shades of green, brown, or maroon and dorsal blotching of an array of colors contrasting with that of the ground color; contrasting postocular stripe absent vs. present); B. thalassinus (moderate to intermediate eleva- tions from extreme eastern Guatemala and extreme northwestern El Salvador to west- ern Honduras) — number of midbody dorsal scale rows (19 vs. 21–23, usually 21), and condition of prelacunal and second supralabial scales (fused vs. separate). (Townsend et al. 2013) 
CommentHabitat: fully arboreal (Harrington et al. 2018). 
Etymology“The specific name guifarroi is a patronym used to honor our colleague and friend, Honduran environmental leader Mario Guifarro of Olancho. Don Mario fearlessly led grassroots efforts to stop illegal logging in the indigenous Tawahka territory of eastern Honduras, despite repeated assassination attempts and threats on his own life and those of his compatriots. Don Mario was murdered on 15 September 2007, ironically Honduras’ Independence Day, while leading a mission to demarcate the boundaries of the Tawahka-Asangni Biosphere and stave off further illegal deforestation. On 21 July 2008, the only witness to Mario’s assassination, his son Shamir Guifarro Ramírez, was also murdered, along with Mario’s father-in-law, Henry Arturo Chacón, and mother-in-law, Nelda Ochoa, after they were followed out of the city of Juticalpa by unknown assailants.” 
References
  • García-Padilla E, DeSantis DL, Rocha A, Mata-Silva V, Johnson JD, Wilson LD. 2020. Conserving the Mesoamerican herpetofauna: the most critical case of the priority level one endemic species. Amphibian & Reptile Conservation 14(2) [General Section]: 73–132 (e240) - 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
  • Mason AJ; Grazziotin F; Zaher H; Lemmon A; Moriarty Lemmon E & Parkinson C 2019. Reticulate evolution in nuclear Middle America causes discordance in the phylogeny of palm-pitvipers (Viperidae: Bothriechis). Journal of Biogeography 46 (5): 833-844 - 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
  • OLIVEIRA-DALLAND, LUIS G.; LAURA R.V. ALENCAR, LEANDRO R. TAMBOSI, PAOLA A. CARRASCO, RHETT M. RAUTSAW, JESUS SIGALA-RODRIGUEZ, GUSTAVO SCROCCHI & MARCIO MARTINS. 2022. Conservation gaps for Neotropical vipers: Mismatches between protected areas, species richness and evolutionary distinctiveness. Biological Conservation 275(109750). - 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
  • Townsend, Josiah; Melissa Medina-Flores, Larry Wilson, Robert Jadin, James Austin 2013. A relict lineage and new species of green palm-pitviper (Squamata, Viperidae, Bothriechis) from the Chortís Highlands of Mesoamerica. ZooKeys 298 (2013): 77-105 - get paper here
  • 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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