Type Locality Restriction of <I>Hypsiglena Torquata</I> Gã¼nther

Total Page:16

File Type:pdf, Size:1020Kb

Type Locality Restriction of <I>Hypsiglena Torquata</I> Gã¼nther Great Basin Naturalist Volume 57 Number 1 Article 11 3-7-1997 Type locality restriction of Hypsiglena torquata Günther Wilmer W. Tanner Brigham Young University Follow this and additional works at: https://scholarsarchive.byu.edu/gbn Recommended Citation Tanner, Wilmer W. (1997) "Type locality restriction of Hypsiglena torquata Günther," Great Basin Naturalist: Vol. 57 : No. 1 , Article 11. Available at: https://scholarsarchive.byu.edu/gbn/vol57/iss1/11 This Note is brought to you for free and open access by the Western North American Naturalist Publications at BYU ScholarsArchive. It has been accepted for inclusion in Great Basin Naturalist by an authorized editor of BYU ScholarsArchive. For more information, please contact [email protected], [email protected]. Great Basin Naturalist 57(1), e 1997, pp. 79-82 TYPE LOCALITY RESTRICTION OF HYPSIGLENA TORQUATA GUNTHER Wilmer W Tannerl Key word.s: Hypsiglena lOrquata, Mexico, Nicaroguo.. Since the description ofHIJPsigl.ena torquata type when compared with specimens from by Giinther in 1860 and the designation of the Mazatlan, Sinaloa. He communicated his con­ type locality as Nicaragua, specimens have cern with Mr. J. C. Battersby at the British been collected only in central Mexico and Museum, who prOVided basic character infor­ north into the United States (Tanner 1946, mation for the type specimen. Dixon then con­ Dixon and Dean 1986). Just how far south in cluded that "the locality from which the type Mexico Hypsiglena may range is perhaps not specimen came is somewhat in doubt" and that yet known. Specimens have been taken in "until both co-types are examined and further Morelos, Guerrero, and Michoacan but not as collecting done, it would be unwise to change yet, to my knowledge, from the states of Mex­ the type locality, even though it appears to be ico, Puebla, Veracruz, Oaxaca, or Chiapas. If m. error." HIJPsigiena occurs in Nicaragua, the question The original description of Leptockira tor­ arises as to why additional specimens have not quata Gunther 1860 provides not only an ade­ been taken from the intervening areas. quate description based on scale patterns but There is now general agreement that Hyp­ also includes a draWing of the type specimen siglena does not occur south of Mexico, and (Fig. lA). The draWing exhibits a color pattern perhaps not in southern Mexico; however, that is similar to most specimens seen from Smith and Taylor (1945) list it as "perhaps to south central Mexico and is apparently repre­ Ecuador and Venezuela." Peters (1956) dis­ sentative of H. torquato from that area (Figs. cusses in detail the specimens responsible for IB, C, D). The ventral-caudal counts of 174­ placing HIJPsigl.ena in South America and con­ 174-46-50 listed in the origin.l description cludes that this genus does not occur south of total 220-224 for the two type specimens. This Costa Rica. Peters and Orejas-Miranda (1970) does not match the totals for specimens ofH. t. list the distribution of H. torquata as "South­ torquata listed from west central Mexico (Dixon western United States through Mexico and and Dean 1986). A series of 27 specimens that Baja Galifornia to Costa Rica." Savage and Villa (1986) do not include it in their Herpetofauna I have examined from Guanajuato, Guerrero, of Costa Rica, and Villa et al. (1988) do not list Morelos, Michoacan, J.lisco, and Colina have a it in their Middle American Herpetology. ventral-caudal range of202.--214. Ifthe ventrai­ Peters and Orejas-Miranda (1970) list it only to caudal counts for the types are correct as listed Costa Rica, without including additional records; in the original description, it would be difficult Savage and Villa (1986) and Villa et al. (1988) to include them in the populations of H. t. exclude Hypsiglerw from areas south of Mex­ torquata ofcentral and southwestern Mexico. ico. Dunn (1936:6) lists a specimen from Costa To verify the accuracy of the published data Rica (Museo Nacional) but provides no museum for the type, I contacted Dr. Colin McCarthy number. at the British Natur.l HistOlY Museum for Dixon (1965) recognized that there was a additional information concerning collecting problem in accepting Nicaragua as the type documentation and the accuracy of the scale locality for Hypsiglerw torquata Gunther. This counts published by Gunther (1860). The fol­ he based on the similar color pattern of the lowing response was received: 1M. L. Bean Ufe Science Museum, Brighun Young Unive:nlty, Provo, UT 84602. 79 80 GREAT BASIN NATURALIST [Volume 57 A c D •" B Fig. L Hypsiglena torquata. A, Drawing of Leptodeira torqu<lfa, as figured by Gunther (1860). B, C, D, Photos of speci­ mens ofH. t. torquata taken in west central Mexico: Band C, LACM 7269, 58.4 miles SE of Escuinapa, Nayarit; D, BYO 23787,25 miles S ofEI Salado, Sinaloa, Mexico. I am afraid that there is no additional documentary origin in central Mexico. The scale and color evidence here regarding the collectors of the speci­ patterns could place it in one ofthe states listed mens. I note that we received it from the Derby Museum, so I imagine that if there was ever any above or perhaps in one of several adjoining associated documentation of that sort it might be states. there. The Derby Museum is still in existence Other scale patterns of the type specimen though without any names or reference numbers I taken from the original description are similar would have thought it would be impossible for them to provide information. to specimens from central and western Mexico. Quoting Gunther (1860): "The medial lower Dr. McCarthy provided the following data labial is triangular and rather small; nine lower for the type specimen, 46.1.1.15 (formerly labials, the Ilrst of which is in contact with its 61.12.30.97 as published by Smith and Taylor fellow behind the median shield." One speci­ 1945): "ventrals 170 (Dowling count, add 2 if men (Taylor 5561, a female) from a series of 8 you prefer to couut from the first expanded specimens from Morelos has nearly all scale scale). Subcaudals 42 pairs (+1 terminal scale). pattern characteristics of the type specimen: It appears to be a female." ventrais 171, pre- and post-oculars 2-2, infra­ In counting ventrals I have always started labials 9-9, temporals 1-2. The only difference with the Ilrst scale that is noticeably wider is that the type has 8-8 supralabials rather than than long. It appears that there are in tb e type 7-7 as in the Taylor specimen. However, other 2 questionable scales that Dowling considered specimens from Morelos have 8-8 supralabials. gulars; they might be small ventrals. In count­ A specimen (USNM 46513 female) from ing caudals I have always included the termi­ Michoacan has 173 ventrals, 39 caudals (total nal scale in the count. Based on the present 212), and 9-10 infralabials. Other specimens data, ventrals of the type are either 170 or 172 from west central Mexico also approach the and caudals 43. These add to 213 or 215 ven­ scale pattern of the type based on the recount tral-caudals for the type specimen in the ofventrals and caudals ofthe type. British Museum, which is within the range for By carefully examining the drawing of the females in populations ofcentral or southwest­ type (Fig. 1A), oue can see that the artist ern Mexico. appears to have virtually duplicated the color The present information is not sufficient to pattern of tbe entire snake. The head, nape, place the type locality at a given location, but it and body pattern are near duplicates of some does provide sufflcient data to place the area of specimens from Mexico. The whi> band is 1997] NOTES 81 about 4 scales in length and the dark nape Liverpool wrote anything to suggest that they band 6 or 7. In the series from Morelos, the tllought it was in Nicaragua. On the contrary, Giin­ ther clearly states that his material was believed to white band is 4-5 scales long and the dark one originate from two quite separate places and mod­ 5-6 long. Dorsal body spots range fi'om 45 to ern citations of the type locality as "Laguna Island, 52. In the drawing of the type, I count 43, and Nicaragua" seem totally unjustified. In short, I sus­ there are some hidden by the head. If this is, pect that you have good reason to worry about the and it appears to be, an essentially accurate provenance of these specimens, hecause I can find no very compelling evidence that either snake came drawing ofthe type, it seemingly places it with from Nicaragua!! the Hypsiglena from west cenb·a1 Mexico. Malcom Largen, Curator of The color patterns are helpful in placing the Amphibians and Reptiles type in any of the listed Mexican states, but it is the scale patterns such as the ventral-caudal All data and the information from England totals and the infralabials that effectively relate seemed to confirm my conclusion that the types of H. Gunther had apparently the type to west central Mexico, perhaps to torquato either Marelos or Michoacan. come from Morelos, Mexico. I sent a rough In the original description 2 specimens were draft ofthe manuscript to Dr. Hobart M. Smith available to Gunther. I asked Dr. McCarthy if for his perusal and for any comments he might he knew the location of the 2nd specimen. He provide. His response is as follows: referred me to Mr. Malcom Largen at the Liver­ Isla Laguna makes no sense as a locality, but there pool Museum.
Recommended publications
  • A Taxonomic Study of the Genus Hypsiglena
    Great Basin Naturalist Volume 5 Number 3 – Number 4 Article 1 12-29-1944 A taxonomic study of the genus Hypsiglena Wilmer W. Tanner Provo High School Follow this and additional works at: https://scholarsarchive.byu.edu/gbn Recommended Citation Tanner, Wilmer W. (1944) "A taxonomic study of the genus Hypsiglena," Great Basin Naturalist: Vol. 5 : No. 3 , Article 1. Available at: https://scholarsarchive.byu.edu/gbn/vol5/iss3/1 This Article is brought to you for free and open access by the Western North American Naturalist Publications at BYU ScholarsArchive. It has been accepted for inclusion in Great Basin Naturalist by an authorized editor of BYU ScholarsArchive. For more information, please contact [email protected], [email protected]. ., .The Great Basin Naturalist 7>^^ of Comai;^^ Published by the A«'*^ Zootomy 'U\ I^KH.MMMKNT OF ZoOI.OC.Y AND ExTOMOI.OCV UtInrT i.99»fl46*) J BiMCHAM Young UxiVEKsny. Pkovo, Utah v.,-- / B K A Hj* Volume V DECEMBER 29, 1944 Nos. 3 & 4 )\( I A TA.\( ).\JK- STL'I)\' OV TH1^ GENUS 1 IN' 'Sl( ilJ-.XA WII.MI-'.K W. TANNKRi I'r.jvo Higli ScIkxiI. Provo, Utah IXTKODUe'lION In ihc Course ol my studies of Utah specimens of the genus Hypsiglena it became apparent that 1 could better understand this genus if a large series of specimens were secured for study. Accord- ingl_\- 1 set out tcj bring together by loan as many specimens as possible. As a result over 4(XJ specimens have been assembled and studied. This C(nil(l not have been accomplished without the aid of many workers and insiiiutions who ha\e so graciously allowed me to stutly their specimens.
    [Show full text]
  • Microhabitat and Prey Odor Selection in Hypsiglena Chlorophaea
    Copeia 2009, No. 3, 475–482 Microhabitat and Prey Odor Selection in Hypsiglena chlorophaea Robert E. Weaver1 and Kenneth V. Kardong1 We studied the effects of various shelter and prey odor combinations on selection of microhabitat characters by the Desert Nightsnake, Hypsiglena chlorophaea, a dipsadine snake. We also examined the activity patterns of these snakes over a 23-h period. Three prey odors were tested, based on field work documenting natural prey in its diet: lizard, snake, mouse (plus water as control). In the first experiment, each odor was tested separately in various shelter and odor combinations. We found that snakes preferred shelter to no shelter quadrants, and most often selected a quadrant if it also had prey odor in the form of lizard or snake scent. However, snakes avoided all quadrants containing mouse (adult) odor. In the second experiment, all three odors plus water were presented simultaneously. We found that snakes showed a preference for lizard odor over the others, but again showed an aversion to mouse odor, even compared to water. The circadian rhythms in both experiments showed generally the same pattern, namely an initial peak in activity, falling off as they entered shelters, but then again increasing even more prominently from lights off until about midnight. Thereafter, activity tapered off so that several hours before lights on in the morning, snakes had generally taken up residence in a shelter. Prey preference correlates with field studies of dietary frequency of lizards, while activity exhibits strong endogenous nocturnal movement patterns. EVERAL factors may influence habitat preference and (Stebbins, 2003), with an abundance of lizards, on which circadian patterns of activity.
    [Show full text]
  • Rediscovery of an Endemic Vertebrate from the Remote Islas Revillagigedo in the Eastern Pacific Ocean: the Clario´N Nightsnake Lost and Found
    Rediscovery of an Endemic Vertebrate from the Remote Islas Revillagigedo in the Eastern Pacific Ocean: The Clario´n Nightsnake Lost and Found Daniel G. Mulcahy1*, Juan E. Martı´nez-Go´ mez2, Gustavo Aguirre-Leo´ n2, Juan A. Cervantes-Pasqualli2, George R. Zug1 1 Department of Vertebrate Zoology, National Museum of Natural History, Smithsonian Institution, Washington DC, United States of America, 2 Instituto de Ecologı´a, Asociacio´n Civil, Red de Interacciones Multitro´ficas, Xalapa, Veracruz, Me´xico Abstract Vertebrates are currently going extinct at an alarming rate, largely because of habitat loss, global warming, infectious diseases, and human introductions. Island ecosystems are particularly vulnerable to invasive species and other ecological disturbances. Properly documenting historic and current species distributions is critical for quantifying extinction events. Museum specimens, field notes, and other archived materials from historical expeditions are essential for documenting recent changes in biodiversity. The Islas Revillagigedo are a remote group of four islands, 700–1100 km off the western coast of mainland Me´xico. The islands are home to many endemic plants and animals recognized at the specific- and subspecific-levels, several of which are currently threatened or have already gone extinct. Here, we recount the initial discovery of an endemic snake Hypsiglena ochrorhyncha unaocularus Tanner on Isla Clario´n, the later dismissal of its existence, its absence from decades of field surveys, our recent rediscovery, and recognition of it as a distinct species. We collected two novel complete mitochondrial (mt) DNA genomes and up to 2800 base-pairs of mtDNA from several other individuals, aligned these with previously published mt-genome data from samples throughout the range of Hypsiglena, and conducted phylogenetic analyses to infer the biogeographic origin and taxonomic status of this population.
    [Show full text]
  • Predation on the Black-Throated Sparrow Amphispiza Bilineata
    Herpetology Notes, volume 13: 401-403 (2020) (published online on 26 May 2020) Predation on the black-throated sparrow Amphispiza bilineata (Cassin, 1850) and scavenging behaviour on the western banded gecko Coleonyx variegatus (Baird, 1858) by the glossy snake Arizona elegans Kennicott, 1859 Miguel A. Martínez1 and Manuel de Luna1,* The glossy snake Arizona elegans Kennicott, 1859 is Robles et al., 1999a), no specific species have been a nocturnal North American colubrid found from central identified as a prey item until this paper, in which we California to southwestern Nebraska in the United States present evidence of predation on the black-throated and south through Baja California, Aguascalientes, San sparrow Amphispiza bilineata (Cassin, 1850). Luis Potosí and Sinaloa in Mexico (Dixon and Fleet, On 20 September 2017, at around 23:00 h, an 1976). Several species have been identified as prey adult specimen of Arizona elegans was found in the items of this snake (Rodríguez-Robles et al., 1999a) municipality of Hipólito (25.7780 N, -101.4017 W, including the mole Scalopus aquaticus (Linnaeus, 1758) 1195 m a.s.l.), state of Coahuila, Mexico. The snake (Eulipotyphla: Talpidae), the rodents Peromyscus sp. had caught and was in the process of killing and then (Rodentia: Cricetidae), Chaetodipus formosus (Merriam, consuming a small bird (Fig. 1); this act lasted close to 1889), Dipodomys merriami Mearns, 1890, Dipodomys 30 minutes. After completely swallowing its prey, the ordii Woodhouse, 1853, Dipodomys sp., Perognathus snake crawled away to a safe spot under a group of inornatus Merriam, 1889, Perognathus (sensu lato) sp. nearby dead Agave lechuguilla plants.
    [Show full text]
  • Reptiles Squamata/Charinidae [ ] Lichanura Trivirgata Rosy Boa
    National Park Service U.S. Department of the Interior Species Checklist for Mojave National Preserve (MOJA) This species list is a work in progress. It represents information currently in the NPSpecies data system and records are continually being added or updated by National Park Service staff. To report an error or make a suggestion, go to https://irma.nps.gov/npspecies/suggest. Scientific Name Common Name Reptiles Squamata/Charinidae [ ] Lichanura trivirgata rosy boa Squamata/Colubridae [ ] Arizona elegans glossy snake [ ] Chionactis occipitalis western shovel-nosed snake [ ] Coluber flagellum coachwhip [ ] Coluber taeniatus striped whipsnake [ ] Diadophis punctatus ring-necked snake [ ] Hypsiglena chlorophaea desert nightsnake [ ] Lampropeltis californiae California kingsnake [ ] Phyllorhynchus decurtatus spotted leaf-nosed snake [ ] Pituophis catenifer gopher snake [ ] Rhinocheilus lecontei long-nosed snake [ ] Salvadora hexalepis western patch-nosed snake [ ] Sonora semiannulata western groundsnake [ ] Tantilla hobartsmithi Smith's black-headed snake [ ] Trimorphodon biscutatus California lyresnake Squamata/Crotaphytidae [ ] Crotaphytus bicinctores Great Basin collared lizard [ ] Gambelia wislizenii long-nosed leopard lizard Squamata/Eublepharidae [ ] Coleonyx variegatus western banded gecko Squamata/Helodermatidae [ ] Heloderma suspectum gila monster Squamata/Iguanidae [ ] Dipsosaurus dorsalis desert iguana [ ] Sauromalus ater common chuckwalla [ ] Sceloporus occidentalis western fence lizard [ ] Sceloporus uniformis yellow-backed
    [Show full text]
  • Crotalus Tancitarensis. the Tancítaro Cross-Banded Mountain Rattlesnake
    Crotalus tancitarensis. The Tancítaro cross-banded mountain rattlesnake is a small species (maximum recorded total length = 434 mm) known only from the upper elevations (3,220–3,225 m) of Cerro Tancítaro, the highest mountain in Michoacán, Mexico, where it inhabits pine-fir forest (Alvarado and Campbell 2004; Alvarado et al. 2007). Cerro Tancítaro lies in the western portion of the Transverse Volcanic Axis, which extends across Mexico from Jalisco to central Veracruz near the 20°N latitude. Its entire range is located within Parque Nacional Pico de Tancítaro (Campbell 2007), an area under threat from manmade fires, logging, avocado culture, and cattle raising. This attractive rattlesnake was described in 2004 by the senior author and Jonathan A. Campbell, and placed in the Crotalus intermedius group of Mexican montane rattlesnakes by Bryson et al. (2011). We calculated its EVS as 19, which is near the upper end of the high vulnerability category (see text for explanation), its IUCN status has been reported as Data Deficient (Campbell 2007), and this species is not listed by SEMARNAT. More information on the natural history and distribution of this species is available, however, which affects its conservation status (especially its IUCN status; Alvarado-Díaz et al. 2007). We consider C. tancitarensis one of the pre-eminent flagship reptile species for the state of Michoacán, and for Mexico in general. Photo by Javier Alvarado-Díaz. Amphib. Reptile Conserv. | http://amphibian-reptile-conservation.org 128 September 2013 | Volume 7 | Number 1 | e71 Copyright: © 2013 Alvarado-Díaz et al. This is an open-access article distributed under the terms of the Creative Commons Attribution–NonCommercial–NoDerivs 3.0 Unported License, which permits unrestricted use for Amphibian & Reptile Conservation 7(1): 128–170.
    [Show full text]
  • Boletín De Prensa
    Comisión Nacional para el Conocimiento y Tel. (5255) 5004-5000 Uso de la Biodiversidad Fax. (5255) 5004-4931 Liga Periférico-Insurgentes Sur 4903 www.conabio.gob.mx Col. Parques del Pedregal, Del. Tlalpan 14010 México, D.F. Nota informativa 20 de mayo de 2014 Nota informativa CONABIO Núm. 66 México, D. F. LA SERPIENTE NOCTURNA DE LA ISLA CLARIÓN Identificada, desaparecida, reencontrada Imagen cortesía del Dr. Juan Esteban Martínez-Gómez / INECOL Serpiente nocturna de la Isla Clarión 20-May-2014. Una nueva especie de culebra se descubre en la isla mexicana más remota. El redescubrimiento de la culebra nocturna de la Isla Clarión marca todo un acontecimiento ya que no se había registrado desde 1936. En su reencuentro, el reptil se describe como una especie distinta de serpiente endémica de la isla. La descripción sale a la luz pública a un año de la expedición realizada por los investigadores que redescubrieron la especie entre mayo y junio de 2013 y coincidiendo con la 4ª. Semana de la Diversidad Biológica que se celebra en el país del 14 al 25 de mayo de 2014 y que tiene como tema Islas y biodiversidad www.biodiversidad.gob.mx/SDB. Las islas son el hogar de muchas plantas y animales endémicos, es decir, con distribución restringida a un espacio definido; varias de estas especies están actualmente amenazadas o ya se han extinguido. México posee más de mil islas; entre ellas, un grupo remoto de cuatro pequeños territorios conforman el Archipiélago de Revillagigedo: Isla Socorro, Isla San Benedicto, Isla Clarión y el Islote Roca Partida, pertenecientes al estado de Colima y ubicados entre los 700 y 1100 km de distancia con respecto a las costas en tierra firme.
    [Show full text]
  • Chapter 4: Amphibians and Reptiles
    1 Chapter 4: Amphibians and Reptiles The history of amphibians, reptiles, and even our own species, is an epic journey through time. But exactly how long? A hundred years ago? A thousand? A million? Well, what about 380 million years ago? Why so long? Well, everything just seems to take a lot longer than we think it should. Just think about how long it takes to get ready in the morning—or do a math assignment! It takes time to move continents, make new species, and change the world. Between 416 and 359 million years ago, the Earth started to change. This time period is called the Devonian. Somewhere around 380 million years ago, the first amphibians began making their way onto land, making them the first animals with a spine to do so. They were able to do this because they had developed lungs - allowing them to breathe oxygen by getting it straight from the air. This was a huge advantage because the oceans were running out of oxygen. Amphibians then, and even now, needed water to lay their eggs. Their eggs are soft and gooey. Without a shell to protect them, they will dry up and die. So remember— if you are trying to find an amphibian, find water first! After the amphibians made their way onto land, some of them started to change again. Some created eggs that had a leathery or hard shell. This one ad- aptation gave rise to the reptiles. Rep- tiles first appear in the Carboniferous period (359.2 million years to about 299.0 million years ago).
    [Show full text]
  • Life History Account for Desert Nightsnake
    California Wildlife Habitat Relationships System California Department of Fish and Wildlife California Interagency Wildlife Task Group DESERT NIGHTSNAKE Hypsiglena chlorophaea Family: COLUBRIDAE Order: SQUAMATA Class: REPTILIA R071 Written by: S. Morey Reviewed by: T. Papenfuss Edited by: R. Duke Updated by: CWHR Staff, November 2014 DISTRIBUTION, ABUNDANCE, AND SEASONALITY The desert nightsnake is locally common in suitable habitat in southern California deserts and from isolated localites in northern Siskiyou and eastern Modoc Co., although nightsnakes probably range throughout much of arid northeastern California. Found in a variety of desert shrub habitats. Elevation sea level to 1920 m (7000 ft). The species has been split and is now considered separate from H. ochrorhyncha, SPECIFIC HABITAT REQUIREMENTS Feeding: The saliva of this snake is mildly venomous, which may help them secure small prey, especially lizards and occasional amphibians (Stebbins 1954). Cover: When not active this snake seeks cover in crevices in rocky outcrops, under surface objects, and in mammal burrows. The subterranean tendencies of this snake are evidenced by its being found occasionally by roadbuilding crews. Reproduction: The eggs of this species are laid in crevices in rocky accumulations. Abandoned mammal burrows may also occasionally be utilized as nest sites. Water: No information on water requirements. This is a snake of arid regions and is often found far from standing water, which is not considered to be an important habitat element. Pattern: Nightsnakes are most commonly associated with rocky areas or rock outcrops in a variety of habitats. SPECIES LIFE HISTORY Activity Patterns: Nocturnal and crepuscular, night snakes are almost never encountered abroad during the day.
    [Show full text]
  • Conservation Status of the Herpetofauna of Baja California, México and Associated Islands in the Sea of Cortez and Pacific Ocean
    Herpetological Conservation and Biology 4(3):358-378. Submitted: 3 June 2009; Accepted: 11 October 2009. CONSERVATION STATUS OF THE HERPETOFAUNA OF BAJA CALIFORNIA, MÉXICO AND ASSOCIATED ISLANDS IN THE SEA OF CORTEZ AND PACIFIC OCEAN 1, 4 2 3 ROBERT E. LOVICH , L. LEE GRISMER , AND GUSTAVO DANEMANN 1Department of Earth and Biological Sciences, Loma Linda University, Loma Linda, California 92350,USA, 2Department of Biology, LaSierra University, Riverside, California, 92515 USA 3Pronatura Noroeste, Calle Décima Nº60, Zona Centro, Ensenada, Baja California, CP 22800, México 4Present Address: Naval Facilities Engineering Command, Southwest;1220 Pacific Highway, San Diego, California 92132, USA, e-mail: [email protected] Abstract.—The herpetofauna of the Baja California Peninsula represent a unique assemblage of the biodiversity and heritage of México. Pressure from increasing development and land conversion of the second longest peninsula in the world, and its islands, requires a modern synthesis of the conservation status of the herpetofauna. Herein, we evaluate the herpetofauna by assessing regulatory protections, natural protected land areas, and maintenance of ex situ species in accredited zoos. We also summarize recent changes to the taxonomy and nomenclature for this herpetofauna, as well as range extensions that further our understanding of species distributions, many of which are poorly understood. Recommendations are given to enhance and further strengthen conservation actions in Baja California, México. Key Words.—amphibians, Baja California, conservation, México, reptiles, Sea of Cortez INTRODUCTION the northwest Pacific Coast. Inland from the northern peninsula are the highest elevations comprising The Baja California Peninsula, in northwestern chaparral, oak woodland, and coniferous forest México, consists of the states of Baja California and communities (Wiggins 1980).
    [Show full text]
  • Coalescent Species Tree Inference of Coluber and Masticophis
    Copeia 105, No. 4, 2017, 642–650 Coalescent Species Tree Inference of Coluber and Masticophis Edward A. Myers1, Jamie L. Burgoon1, Julie M. Ray2, Juan E. Mart´ınez-Gomez´ 3, Noem´ı Mat´ıas-Ferrer4,5, Daniel G. Mulcahy6, and Frank T. Burbrink1 The genus-level taxonomy of the New World racers and whipsnakes (Coluber and Masticophis) has long been contentious regarding whether the two genera are mutually exclusive clades. This argument is based on morphological characters and largely single-locus analyses. Herein we examine the phylogenetic history of this group using multi-locus data in a coalescent framework, where paraphyly of Masticophis would result in support for the recognition of only a single genus (Coluber) for these species. We sample all currently recognized species and incorporate broad geographic sampling for the more widespread species groups to explore biogeographic patterns across North America. Our analyses suggest that Masticophis is monophyletic with respect to Coluber constrictor, albeit with low support. These results also demonstrate that there is undescribed cryptic diversity in this group, and we underscore additional avenues of study to further delimit unrecognized species in this clade. The biogeography of the island endemic, Masticophis anthonyi, is discussed with respect to what is known about other codistributed vertebrates. Lastly we provide an overview of the history of the arguments for or against the use of the generic name Masticophis and suggest its continued use. T is widely accepted that higher-level taxonomy should incompatible with the species history due to incomplete reflect evolutionary history, and while most modern lineage sorting (Edwards, 2009), a situation often exacerbated I researchers agree on this general principle, often current by rapid species diversification (e.g., Koblmuller¨ et al., 2010).
    [Show full text]
  • Reptiles and Amphibians
    Reptiles and Amphibians The McLaughlin Reserve has many of the typical reptile and amphibian (“herptile”) species of the Coast Range. In chaparral and oak woodland are western fence lizards and California whiptail lizards. In ponds and streams are California newts and rough- skinned newts. Some species that are common in similar habitats, such as the Coast Horned Lizard and the Ensatina (a large orange-and-brown spotted salamander) have surprisingly not been found at the reserve. Other species yet to be sighted include the arboreal salamander (Aneides lugubris), California slender salamander (Batrachoseps attenuatus), coachwhip (Masticophis flagellum), long-nosed snake (Rhinocheilus lecontei), night snake (Hypsiglena torquata), rubber boa (Charina bottae), and sharp- tailed snake (Contia teuis). The reserve is not known to have any rare herptile species. The herptile fauna of the McLaughlin Reserve has not yet been the subject of University research, but it is relatively well known from the pre-mine survey by the D’Appolonia company and the subsequent wildlife records kept by Homestake. These reports were used to generate the locality information and species list given here. Species descriptions have been adapted from the references by Basey (1991), Leviton (1971), and Stebbins (1972). A good field guide to herptiles of this area is Robert Stebbins’ (1972) Amphibians and Reptiles of California. Lizards California whiptails (Cnemidophorous tigris) are slender lizards that appear “jumpy” or “nervous”. They have a tail about twice as long as their bodies. When foraging they move their head frequently, shaking it from side to side. They are brownish with a striped pattern of white and brown scales and a bluish tail.
    [Show full text]