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Crotalus unicolor LIDTH DE JEUDE, 1887

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Higher TaxaViperidae, Crotalinae, Colubroidea, Caenophidia, Alethinophidia, Serpentes, Squamata (snakes)
Subspecies 
Common NamesE: Aruba Island Rattlesnake
G: Aruba-Klapperschlange 
SynonymCrotalus horridus var. unicolor LIDTH DE JEUDE 1887: 133
Crotalus unicolor — KLAUBER 1936: 190
Crotalus durissus unicolor — DAAN & HILLENIUS 1966: 137
Crotalus unicolor — MCCRANIE 1986
Crotalus durissus unicolor — CAMPBELL & LAMAR 1989
Crotalus durissus unicolor — WELCH 1994: 45
Crotalus durissus unicolor — MCDIARMID et al. 1999
Crotalus durissus unicolor — CAMPBELL & LAMAR 2004
Crotalus durissus unicolor — QUIJADA-MASCAREÑAS & WÜSTER 2006
Caudisona unicolor — HOSER 2009
Crotalus unicolor — MARITZ et al. 2016
Crotalus unicolor — ZAHER et al. 2019 
DistributionAruba Island (off the coast of Venezuela)

Type locality: “Aruba”  
Reproductionovovivparous. Schuett et al. (1997) provide evidence for parthenogenesis in this C. d. unicolor. 
TypesHolotype: RMNH 613 
DiagnosisDIAGNOSIS. Crotalus unicolor is a stunted species related to C. durissus, ranging in size from about 230 mm at birth to 970 mm in the largest known specimen. Adults are pale gray or pale grayish brown dorsally with faint or nearly indistinguishable dorsal rhombs. Longitudinal stripes on the rear part of the head and on the neck are faintly evident in some adults and indistinguishable in others. When evident, the dorsal rhombs number 18 to 28. The venter is white or cream-colored. The tail is darker gray than the body. Juveniles have distinct dorsal rhombs and longitudinal stripes on the rear part of the head and on the neck. Traces of a frontal crossbar, a dark supraocular stripe, and 5-6 caudal crossbands are evident in some juveniles. All of these markings fade with age. Scutellation is as follows: 25-27 (usually 27) scale rows at midbody, all keeled except for the lowest 1-3; 155-164 ventrals in males, 163-169 in females; 26-31 subcaudals in males, 22-25 in females; 11-15 supralabials; 12-16 infralabials (first frequently divided); 2 preoculars. The rostral is triangular and higher than wide. The internasals are paired. The prefrontals are paired, in contact medially, and are larger than the internasals. Posterior to the prefrontals (frontal area) there are two large scales bordered posteriorly by smaller irregular scales in rows. Posterior to these irregular scales there is a pair of larger scales (vestiges of parietals) bordering the supraoculars. The remainder of the head is covered by small and fairly regular scales. The first supralabial contacts the prenasal. There are 1-3 loreals on each side of the head. A vertebral ridge is present in adults but is less pronounced than in Crotalus durissus. Crotalus unicolor differs from C. durissus in that the dorsal rhombs and the pair of longitudinal stripes present on the head and neck of durissus are largely absent in adult unicolor because of a faded color pattern. Crotalus unicolor is also a smaller species than durissus, with the largest known specimen of unicolor 970 mm in total length. Crotalus unicolor differs from C. vegrandis, another stunted species closely related to durissus, in that the latter has numerous scattered white-tipped scales on the head and body. (McCranie 1986)


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CommentVenomous! 
EtymologyNamed after Latin uni (meaning one) and color (meaning color), refering to the faded color pattern of the species. 
References
  • Booth, Warren; Gordon W. Schuett 2015. The emerging phylogenetic pattern of parthenogenesis in snakes. Biological Journal of the Linnean Society 118 (2): 172–186, DOI: 10.1111/bij.12744
  • Campbell, J.A. & Lamar, W.W. 1989. The Venomous Reptiles of Latin America. Comstock Publishing/Cornell University Press, Ithaca
  • Campbell, Jonathan A. and William W. Lamar 2004. The Venomous Reptiles of the Western Hemisphere, 2 vols. Comstock (Cornell University Press), Ithaca, NY, 962 pp. [review in Science 305: 182]
  • Daan, S. & Hillenius,D. 1966. Catalogue of the type specimens of amphibians and reptiles in the Zoological Museum, Amsterdam. Beaufortia 13: 117-144
  • Hoser, R. 2009. A reclassification of the rattlesnakes; species formerly exclusively referred to the genera Crotalus and Sistrurus. Australasian J. Herpetol. 3: 1-21 - get paper here
  • Klauber, Laurence M. 1936. A key to the rattlesnakes with summary of characteristics. Transactions of the San Diego Society of Natural History 8 (20): 185-276 + 1 foldout table - get paper here
  • Lidth de Jeude, Th. W. van. 1887. On a collection of reptiles and fishes from the West-Indies. Notes from the Leyden Museum 9: 129—139. - get paper here
  • Maritz, Bryan; Johannes Penner, Marcio Martins, Jelka Crnobrnja-Isailović, Stephen Spear, Laura R.V. Alencar, Jesús Sigala-Rodriguez, Kevin Messenger, Rulon W. Clark, Pritpal Soorae, Luca Luiselli, Chris Jenkins, Harry W. Greene 2016. Identifying global priorities for the conservation of vipers. Biological Conservation, doi:10.1016/j.biocon.2016.05.004 - get paper here
  • McCranie J R 1986. Crotalus unicolor van Lidth de Jeude. Aruba Island rattlesnake. Catalogue of American Amphibians and Reptiles ( 389: 1-2 - get paper here
  • McDiarmid, R.W.; Campbell, J.A. & Touré,T.A. 1999. Snake species of the world. Vol. 1. [type catalogue] Herpetologists’ League, 511 pp.
  • 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
  • Quijada-Mascareñas & Wüster, W. 2006. Crotalus durissus complex: from Yucatan to Patagonia: the natural history of the Neotropical rattlesnake. Reptilia (GB) (49): 66-73 - get paper here
  • Strimple, Pete 1993. Crotalus unicolor (Van Lidth de Jeude), Aruba island rattlesnake. Litteratura Serpentium 13 (1): 4-13 - get paper here
  • Voort, Marcel van der 2012. Pictures: Crotalus unicolor. Litteratura Serpentium 32 (4): 253 - get paper here
  • Welch, K. R. G. 1994. Snakes of the World. A Checklist. I. Venomous snakes. KCM Books, Somerset, England.
  • Zaher H, Murphy RW, Arredondo JC, Graboski R, Machado-Filho PR, Mahlow K, et al. 2019. Large-scale molecular phylogeny, morphology, divergence-time estimation, and the fossil record of advanced caenophidian snakes (Squamata: Serpentes). PLoS ONE 14(5): e0216148 - get paper here
 
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