Editorial Type:
Article Category: Research Article
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Online Publication Date: 28 Dec 2007

Genealogical Concordance between Mitochondrial and Nuclear DNAs Supports Species Recognition of the Panamint Rattlesnake (Crotalus mitchellii stephensi)

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Page Range: 920 – 932
DOI: 10.1643/0045-8511(2007)7[920:GCBMAN]2.0.CO;2
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Abstract

The Speckled Rattlesnake (Crotalus mitchellii) is a polytypic taxon presently composed of five subspecies that range across southwestern North America, including the Baja Peninsula and islands in the Pacific Ocean and Sea of Cortés. The principles of genealogical concordance were employed to test the taxonomic status of three of the five subspecies (C. m. mitchellii, C. m. pyrrhus, and C. m. stephensi). We used two molecular marker systems: mitochondrial (mt) DNA ATPase 8 and 6 genes (675 base pairs, bp), and introns 5 and 6 of the nuclear (n) DNA ribosomal protein (RP) gene (449 bp). These markers were evaluated across 104 individuals of C. mitchellii: C. m. mitchellii (n  =  3), C. m. pyrrhus (n  =  83), C. m. stephensi (n  =  18), with Sistrurus c. catenatus as the distant outgroup. Deep phylogenetic splits were detected in the subspecies of C. mitchellii, with 5.0–6.4% mtDNA sequence divergence (SD) separating C. m. mitchellii and C. m. pyrrhus, while C. m. mitchellii and C. m. stephensi had SD values of 6.4–7.3%. Similarly, C. m. pyrrhus and C. m. stephensi had SD values of 5.2–6.7%. In addition, C. m. mitchellii and C. m. pyrrhus were identical in all 449 intron bp, but C. m. stephensi differed from both at a single nucleotide polymorphism. Our molecular results diagnose C. m. stephensi as sister to mainland subspecies of the C. mitchellii complex, a result consistent with certain head scalation characters and its northernmost geographic distribution in this complex. Furthermore, four morphological synapomorphies (supraocular scales prominently ridged and/or creased, contact between rostral and prenasal scales, ground coloration of tail congruent with that of body, and black rings in the distal 15% of the tail) also diagnose C. m. stephensi from all other subspecies of C. mitchellii. We hypothesize that the northern distribution of C. m. stephensi likely resulted from two vicariant events: Pliocene expansion of the Sea of Cortés as the Salton Trough, and Pliocene development of the lacustrine Bouse Embayment along the Colorado River drainage. Despite earlier conclusions based on morphology, our molecular results showed no evidence of intergradation between C. m. pyrrhus and C. m. stephensi. Based on the principles of genealogical concordance, we advocate that C. m. stephensi be elevated to a full species, which renders a minimum of two species within the C. mitchellii clades we examined.

Copyright: 2007 by the American Society of Ichthyologists and Herpetologists
Figure 1
Figure 1

(A) Map depicting the distribution of Crotalus mitchellii, with subspecific designations ( = shaded areas) labeled (insular taxa not depicted). Sample localities (closed circles) and sample numbers (in some instances) correspond to data in the Appendix of Douglas et al. (2006). BC  =  Baja California (Norte), BCS  =  Baja California Sur. (B) Map designating molecular subclades (designated by ellipses) superimposed on the distribution of Crotalus mitchellii. Phylogenetic relationships of the Crotalus mitchellii clades are depicted.


Figure 2
Figure 2

(A) Crotalus mitchellii stephensi (adult male), Mono County, California, 26 September 2001, elevation 2,027 m (photo by Blake L. Thomason); (B) Crotalus mitchellii mitchellii (adult male), Mexico, Baja California Sur, 42 km S. Mulege, 11 October 1988 (photo by Blake L. Thomason); (C) Crotalus mitchellii pyrrhus (adult), Imperial Co., California, 2005 (photo by John Stoklosa); (D) Crotalus mitchellii pyrrhus (adult male), Yuma Co., Arizona, Kofa Mts., June 2001 (photo by Martin J. Feldner).


Figure 3
Figure 3

Relationships among mtDNA haplotypes found in Crotalus mitchellii based on: (A) Maximum likelihood (ML) analysis; (B) Maximum parsimony (MP) tree with bootstrap values. Two outgroup taxa (Sistrurus catenatus and Crotalus m. molossus) were removed to conserve space. CT  =  C. tigris; CMS  =  C. mitchellii stephensi; CMM  =  C. m. mitchellii; CMP  =  C. m. pyrrhus.


Figure 4
Figure 4

Morphological variation of location (and number) of black tail bands in Crotalus mitchellii stephensi: (A) Mono Co. California, 14.3 km N. on Gorge Rd., 1 km E. Hwy. 395, 22 September 2001 (photo by Blake L. Thomason); (B) Inyo Co. California, 2005 (photo by John Stoklosa); (C) Inyo Co. California, 24 km N. Bishop, 23 June 2001 (photo by Louis W. Porras). Arrow in (C) indicates the most basal rattle (which is black) rather than a black tail band.


Contributor Notes

Section editor: J. M. Quattro.

Michael E Douglas, (MED, MRD) Department of Fish, Wildlife and Conservation Biology, Colorado State University, Fort Collins, Colorado 80523-1474, e-mail: (MED) med@inhs.uiuc.edu(GWS) Department of Biology and Center for Behavioral Neuroscience, Georgia State University, Atlanta, Georgia 30303-3088(LWP) 7705 Wyatt Earp Avenue, Eagle Mountain, Utah 84005(BLT) 772 W. Los Altos, Clovis, California 93612. Present addresses: (MED) Ecology and Conservation Science Division, Illinois Natural History Survey, 1816 S. Oak Street, Champaign, Illinois 61820; and (MRD) Biodiversity and Ecological Entomology Division, Illinois Natural History Survey, 1816 S. Oak Street, Champaign, Illinois 61820. E-mail: (MED) med@inhs.uiuc.edu. Send reprint requests to MED.
Received: 22 Mar 2006
Accepted: 06 Mar 2007
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