Anfibios Y Reptiles Del Estado De Jalisco
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Xenosaurus Tzacualtipantecus. the Zacualtipán Knob-Scaled Lizard Is Endemic to the Sierra Madre Oriental of Eastern Mexico
Xenosaurus tzacualtipantecus. The Zacualtipán knob-scaled lizard is endemic to the Sierra Madre Oriental of eastern Mexico. This medium-large lizard (female holotype measures 188 mm in total length) is known only from the vicinity of the type locality in eastern Hidalgo, at an elevation of 1,900 m in pine-oak forest, and a nearby locality at 2,000 m in northern Veracruz (Woolrich- Piña and Smith 2012). Xenosaurus tzacualtipantecus is thought to belong to the northern clade of the genus, which also contains X. newmanorum and X. platyceps (Bhullar 2011). As with its congeners, X. tzacualtipantecus is an inhabitant of crevices in limestone rocks. This species consumes beetles and lepidopteran larvae and gives birth to living young. The habitat of this lizard in the vicinity of the type locality is being deforested, and people in nearby towns have created an open garbage dump in this area. We determined its EVS as 17, in the middle of the high vulnerability category (see text for explanation), and its status by the IUCN and SEMAR- NAT presently are undetermined. This newly described endemic species is one of nine known species in the monogeneric family Xenosauridae, which is endemic to northern Mesoamerica (Mexico from Tamaulipas to Chiapas and into the montane portions of Alta Verapaz, Guatemala). All but one of these nine species is endemic to Mexico. Photo by Christian Berriozabal-Islas. amphibian-reptile-conservation.org 01 June 2013 | Volume 7 | Number 1 | e61 Copyright: © 2013 Wilson et al. This is an open-access article distributed under the terms of the Creative Com- mons Attribution–NonCommercial–NoDerivs 3.0 Unported License, which permits unrestricted use for non-com- Amphibian & Reptile Conservation 7(1): 1–47. -
New State Records for Amphibians and Reptiles from Colima, Mexico
STORERIA OCCIPITOMACULATA OCCIPITOMACULATA Herpetological Review, 2009, 40(1), 117–120. (Northern Red-bellied Snake). USA: IOWA: CHICKASAW CO.: © 2009 by Society for the Study of Amphibians and Reptiles Newell Road 0.2 km N of State Hwy 24 (43.0616°N, 92.2797°W; WGS84). 04 October 2007. Terry J. VanDeWalle. Verifi ed by James New State Records for Amphibians and Reptiles L. Christiansen. DOR specimen deposited in the Drake University from Colima, Mexico Research Collection (DRUC 7298). New county record. Although species is known from a number of adjacent counties, this specimen fi lls a gap in the distributional data in this portion of the state (J. JACOBO REYES-VELASCO* Centro Universitario de Ciencias Biologicas y Agropecuarias L. Christiansen, pers. comm.; http://www.herpnet.net/Iowa-Her- Carretera a Nogales Km. 15.5. Las Agujas, Nextipac, Zapopan, Jalisco, Mexico petology/). The closest record for this species found in the DRUC e-mail: [email protected] is from Bremer County 32.3 km to the south. Submitted by TERRY J. VANDEWALLE (e-mail: ISRAEL ALEXANDER HERMOSILLO-LOPEZ Centro Universitario de Ciencias Biologicas y Agropecuarias [email protected]), and STACEY J. CARLSON, Natu- Carretera a Nogales Km. 15.5. Las Agujas, Nextipac, Zapopan, Jalisco, Mexico ral Resources Consulting, Inc., 2300 Swan Lake Blvd., Suite 200, e-mail: [email protected] Independence, Iowa 50644, USA. CHRISTOPH I. GRÜNWALD 450 Jolina Way. Encinitas California 92024, USA TANTILLA HOBARTSMITHI (Smith’s Black-headed Snake). e-mail: [email protected] USA: TEXAS: IRION CO.: 2.2 air miles SW of Barnhart on CR311 (31.1134667ºN, 101.2040667ºW). -
Xenosaurus Phalaroanthereon Nieto-Montes De Oca, Campbell, and Flores-Villela, 2001
Xenosaurus phalaroanthereon Nieto-Montes de Oca, Campbell, and Flores-Villela, 2001. This knob-scaled lizard is endemic to the state of Oaxaca, where it occurs in the Montañas y Valles del Centro and Sierra Madre del Sur physiographic provinces at elevations from 1,670 (García- Padilla and Mata-Silva, 2014) to 2,185 m. Individuals of this live-bearing species occupy the interior of crevices, usually singly, in small granite boulders located on hillsides covered with oak and pine-oak forest. Populations persist, however, at sites converted to agricultural use, such as cornfields (Lemos-Espinal and Smith, 2005). Its EVS is calculated as 16, which places it in the middle portion of the high vulnerability category (Wilson et al., 2013a), and its IUCN status is Data Deficient. This species is one of 10 members of the monogeneric family Xenosauridae, which is endemic to Mesoamerica. All but one of the species is endemic to Mexico. ' © Elí García-Padilla 5 www.mesoamericanherpetology.com www.eaglemountainpublishing.com The herpetofauna of Oaxaca, Mexico: composition, physiographic distribution, and conservation status VICENTE MATA-SILVA1, JERRY D. JOHNSON1, LARRY DAVID WILSON2, AND ELÍ GARCÍA-PADILLA3 1Department of Biological Sciences, The University of Texas at El Paso, El Paso, Texas 79968-0500, United States. E-mail: [email protected] (Corresponding author); [email protected] 2Centro Zamorano de Biodiversidad, Escuela Agrícola Panamericana Zamorano, Departamento de Francisco Morazán, Honduras. E-mail: [email protected] 3Oaxaca de Juárez, Oaxaca 68023, Mexico. E-mail: [email protected] ABSTRACT: The herpetofauna of Oaxaca is the largest of any state in Mexico, consisting of 106 anurans, 41 salamanders, two caecilians, three crocodylians, 271 squamates, and 19 turtles (total 442 species). -
Amphibian Alliance for Zero Extinction Sites in Chiapas and Oaxaca
Amphibian Alliance for Zero Extinction Sites in Chiapas and Oaxaca John F. Lamoreux, Meghan W. McKnight, and Rodolfo Cabrera Hernandez Occasional Paper of the IUCN Species Survival Commission No. 53 Amphibian Alliance for Zero Extinction Sites in Chiapas and Oaxaca John F. Lamoreux, Meghan W. McKnight, and Rodolfo Cabrera Hernandez Occasional Paper of the IUCN Species Survival Commission No. 53 The designation of geographical entities in this book, and the presentation of the material, do not imply the expression of any opinion whatsoever on the part of IUCN concerning the legal status of any country, territory, or area, or of its authorities, or concerning the delimitation of its frontiers or boundaries. The views expressed in this publication do not necessarily reflect those of IUCN or other participating organizations. Published by: IUCN, Gland, Switzerland Copyright: © 2015 International Union for Conservation of Nature and Natural Resources Reproduction of this publication for educational or other non-commercial purposes is authorized without prior written permission from the copyright holder provided the source is fully acknowledged. Reproduction of this publication for resale or other commercial purposes is prohibited without prior written permission of the copyright holder. Citation: Lamoreux, J. F., McKnight, M. W., and R. Cabrera Hernandez (2015). Amphibian Alliance for Zero Extinction Sites in Chiapas and Oaxaca. Gland, Switzerland: IUCN. xxiv + 320pp. ISBN: 978-2-8317-1717-3 DOI: 10.2305/IUCN.CH.2015.SSC-OP.53.en Cover photographs: Totontepec landscape; new Plectrohyla species, Ixalotriton niger, Concepción Pápalo, Thorius minutissimus, Craugastor pozo (panels, left to right) Back cover photograph: Collecting in Chamula, Chiapas Photo credits: The cover photographs were taken by the authors under grant agreements with the two main project funders: NGS and CEPF. -
Pseudoeurycea Naucampatepetl. the Cofre De Perote Salamander Is Endemic to the Sierra Madre Oriental of Eastern Mexico. This
Pseudoeurycea naucampatepetl. The Cofre de Perote salamander is endemic to the Sierra Madre Oriental of eastern Mexico. This relatively large salamander (reported to attain a total length of 150 mm) is recorded only from, “a narrow ridge extending east from Cofre de Perote and terminating [on] a small peak (Cerro Volcancillo) at the type locality,” in central Veracruz, at elevations from 2,500 to 3,000 m (Amphibian Species of the World website). Pseudoeurycea naucampatepetl has been assigned to the P. bellii complex of the P. bellii group (Raffaëlli 2007) and is considered most closely related to P. gigantea, a species endemic to the La specimens and has not been seen for 20 years, despite thorough surveys in 2003 and 2004 (EDGE; www.edgeofexistence.org), and thus it might be extinct. The habitat at the type locality (pine-oak forest with abundant bunch grass) lies within Lower Montane Wet Forest (Wilson and Johnson 2010; IUCN Red List website [accessed 21 April 2013]). The known specimens were “found beneath the surface of roadside banks” (www.edgeofexistence.org) along the road to Las Lajas Microwave Station, 15 kilometers (by road) south of Highway 140 from Las Vigas, Veracruz (Amphibian Species of the World website). This species is terrestrial and presumed to reproduce by direct development. Pseudoeurycea naucampatepetl is placed as number 89 in the top 100 Evolutionarily Distinct and Globally Endangered amphib- ians (EDGE; www.edgeofexistence.org). We calculated this animal’s EVS as 17, which is in the middle of the high vulnerability category (see text for explanation), and its IUCN status has been assessed as Critically Endangered. -
Literature Cited in Lizards Natural History Database
Literature Cited in Lizards Natural History database Abdala, C. S., A. S. Quinteros, and R. E. Espinoza. 2008. Two new species of Liolaemus (Iguania: Liolaemidae) from the puna of northwestern Argentina. Herpetologica 64:458-471. Abdala, C. S., D. Baldo, R. A. Juárez, and R. E. Espinoza. 2016. The first parthenogenetic pleurodont Iguanian: a new all-female Liolaemus (Squamata: Liolaemidae) from western Argentina. Copeia 104:487-497. Abdala, C. S., J. C. Acosta, M. R. Cabrera, H. J. Villaviciencio, and J. Marinero. 2009. A new Andean Liolaemus of the L. montanus series (Squamata: Iguania: Liolaemidae) from western Argentina. South American Journal of Herpetology 4:91-102. Abdala, C. S., J. L. Acosta, J. C. Acosta, B. B. Alvarez, F. Arias, L. J. Avila, . S. M. Zalba. 2012. Categorización del estado de conservación de las lagartijas y anfisbenas de la República Argentina. Cuadernos de Herpetologia 26 (Suppl. 1):215-248. Abell, A. J. 1999. Male-female spacing patterns in the lizard, Sceloporus virgatus. Amphibia-Reptilia 20:185-194. Abts, M. L. 1987. Environment and variation in life history traits of the Chuckwalla, Sauromalus obesus. Ecological Monographs 57:215-232. Achaval, F., and A. Olmos. 2003. Anfibios y reptiles del Uruguay. Montevideo, Uruguay: Facultad de Ciencias. Achaval, F., and A. Olmos. 2007. Anfibio y reptiles del Uruguay, 3rd edn. Montevideo, Uruguay: Serie Fauna 1. Ackermann, T. 2006. Schreibers Glatkopfleguan Leiocephalus schreibersii. Munich, Germany: Natur und Tier. Ackley, J. W., P. J. Muelleman, R. E. Carter, R. W. Henderson, and R. Powell. 2009. A rapid assessment of herpetofaunal diversity in variously altered habitats on Dominica. -
Crocodylus Moreletii
ANFIBIOS Y REPTILES: DIVERSIDAD E HISTORIA NATURAL VOLUMEN 03 NÚMERO 02 NOVIEMBRE 2020 ISSN: 2594-2158 Es un publicación de la CONSEJO DIRECTIVO 2019-2021 COMITÉ EDITORIAL Presidente Editor-en-Jefe Dr. Hibraim Adán Pérez Mendoza Dra. Leticia M. Ochoa Ochoa Universidad Nacional Autónoma de México Senior Editors Vicepresidente Dr. Marcio Martins (Artigos em português) Dr. Óscar A. Flores Villela Dr. Sean M. Rovito (English papers) Universidad Nacional Autónoma de México Editores asociados Secretario Dr. Uri Omar García Vázquez Dra. Ana Bertha Gatica Colima Dr. Armando H. Escobedo-Galván Universidad Autónoma de Ciudad Juárez Dr. Oscar A. Flores Villela Dra. Irene Goyenechea Mayer Goyenechea Tesorero Dr. Rafael Lara Rezéndiz Dra. Anny Peralta García Dr. Norberto Martínez Méndez Conservación de Fauna del Noroeste Dra. Nancy R. Mejía Domínguez Dr. Jorge E. Morales Mavil Vocal Norte Dr. Hibraim A. Pérez Mendoza Dr. Juan Miguel Borja Jiménez Dr. Jacobo Reyes Velasco Universidad Juárez del Estado de Durango Dr. César A. Ríos Muñoz Dr. Marco A. Suárez Atilano Vocal Centro Dra. Ireri Suazo Ortuño M. en C. Ricardo Figueroa Huitrón Dr. Julián Velasco Vinasco Universidad Nacional Autónoma de México M. en C. Marco Antonio López Luna Dr. Adrián García Rodríguez Vocal Sur M. en C. Marco Antonio López Luna Universidad Juárez Autónoma de Tabasco English style corrector PhD candidate Brett Butler Diseño editorial Lic. Andrea Vargas Fernández M. en A. Rafael de Villa Magallón http://herpetologia.fciencias.unam.mx/index.php/revista NOTAS CIENTÍFICAS SKIN TEXTURE CHANGE IN DIASPORUS HYLAEFORMIS (ANURA: ELEUTHERODACTYLIDAE) ..................... 95 CONTENIDO Juan G. Abarca-Alvarado NOTES OF DIET IN HIGHLAND SNAKES RHADINAEA EDITORIAL CALLIGASTER AND RHADINELLA GODMANI (SQUAMATA:DIPSADIDAE) FROM COSTA RICA ..... -
An Integrative Multi-Approach Workflow Resolves Species Limits in the Southernmost Members of the Liolaemus Kingii Group (Squama
bioRxiv preprint doi: https://doi.org/10.1101/2020.07.02.185025; this version posted July 3, 2020. The copyright holder for this preprint (which was not certified by peer review) is the author/funder. All rights reserved. No reuse allowed without permission. An integrative multi-approach workflow resolves species limits in the southernmost members of the Liolaemus kingii group (Squamata: Liolaemini) Kevin I. Sanchez´ a,∗, Luciano J. Avilaa, Jack W. Sites Jr.b,1, Mariana Morandoa aInstituto Patag´onicopara el Estudio de los Ecosistemas Continentales, Consejo Nacional de Investigaciones Cient´ıficasy T´ecnicas(IPEEC-CONICET), Boulevard Almirante Brown 2915, Puerto Madryn, CT U9120ACD, Argentina bDepartment of Biology and M.L. Bean Life Science Museum, Brigham Young University (BYU), Provo, UT 84602, USA Abstract Recent conceptual and methodological advances have enabled an increasing number of studies to address the problem of species delimitation in a comprehensive manner. This is of particular interest in cases of species whose divergence times are recent, where the con- clusions obtained from a single source of evidence can lead to the incorrect delimitation of entities or assignment of individuals to species. The southernmost species of the Liolaemus kingii group (namely L. baguali, L. escarchadosi, L. sarmientoi, L. tari and the candidate species L. sp. A) show widely overlapping distributions as well as recent mitochondrial divergences, thus phylogenetic relationships and species boundaries are ambiguous. Here we use a comprehensive approach to assess species limits and corroborate their status as independent lineages through the use of four sources of molecular and morphological in- formation (mitochondrial cytochrome-b, nuclear sequences collected by ddRADseq, and linear, meristic and landmark-based morphometrics). -
Biogeographic Analysis Reveals Ancient Continental Vicariance and Recent Oceanic Dispersal in Amphibians ∗ R
Syst. Biol. 63(5):779–797, 2014 © The Author(s) 2014. Published by Oxford University Press, on behalf of the Society of Systematic Biologists. All rights reserved. For Permissions, please email: [email protected] DOI:10.1093/sysbio/syu042 Advance Access publication June 19, 2014 Biogeographic Analysis Reveals Ancient Continental Vicariance and Recent Oceanic Dispersal in Amphibians ∗ R. ALEXANDER PYRON Department of Biological Sciences, The George Washington University, 2023 G Street NW, Washington, DC 20052, USA; ∗ Correspondence to be sent to: Department of Biological Sciences, The George Washington University, 2023 G Street NW, Washington, DC 20052, USA; E-mail: [email protected]. Received 13 February 2014; reviews returned 17 April 2014; accepted 13 June 2014 Downloaded from Associate Editor: Adrian Paterson Abstract.—Amphibia comprises over 7000 extant species distributed in almost every ecosystem on every continent except Antarctica. Most species also show high specificity for particular habitats, biomes, or climatic niches, seemingly rendering long-distance dispersal unlikely. Indeed, many lineages still seem to show the signature of their Pangaean origin, approximately 300 Ma later. To date, no study has attempted a large-scale historical-biogeographic analysis of the group to understand the distribution of extant lineages. Here, I use an updated chronogram containing 3309 species (~45% of http://sysbio.oxfordjournals.org/ extant diversity) to reconstruct their movement between 12 global ecoregions. I find that Pangaean origin and subsequent Laurasian and Gondwanan fragmentation explain a large proportion of patterns in the distribution of extant species. However, dispersal during the Cenozoic, likely across land bridges or short distances across oceans, has also exerted a strong influence. -
Diverse Mite Family Acaridae
Disentangling Species Boundaries and the Evolution of Habitat Specialization for the Ecologically Diverse Mite Family Acaridae by Pamela Murillo-Rojas A dissertation submitted in partial fulfillment of the requirements for the degree of Doctor of Philosophy (Ecology and Evolutionary Biology) in the University of Michigan 2019 Doctoral Committee: Associate Professor Thomas F. Duda Jr, Chair Assistant Professor Alison R. Davis-Rabosky Associate Professor Johannes Foufopoulos Professor Emeritus Barry M. OConnor Pamela Murillo-Rojas [email protected] ORCID iD: 0000-0002-7823-7302 © Pamela Murillo-Rojas 2019 Dedication To my husband Juan M. for his support since day one, for leaving all his life behind to join me in this journey and because you always believed in me ii Acknowledgements Firstly, I would like to say thanks to the University of Michigan, the Rackham Graduate School and mostly to the Department of Ecology and Evolutionary Biology for all their support during all these years. To all the funding sources of the University of Michigan that made possible to complete this dissertation and let me take part of different scientific congresses through Block Grants, Rackham Graduate Student Research Grants, Rackham International Research Award (RIRA), Rackham One Term Fellowship and the Hinsdale-Walker scholarship. I also want to thank Fulbright- LASPAU fellowship, the University of Costa Rica (OAICE-08-CAB-147-2013), and Consejo Nacional para Investigaciones Científicas y Tecnológicas (CONICIT-Costa Rica, FI- 0161-13) for all the financial support. I would like to thank, all specialists that help me with the identification of some hosts for the mites: Brett Ratcliffe at the University of Nebraska State Museum, Lincoln, NE, identified the dynastine scarabs. -
Porthidium Dunni (Hartweg and Oliver, 1938)
Porthidium dunni (Hartweg and Oliver, 1938). Dunn’s Hognosed Pitviper is a “priority two species” that has been assessed Environmental Vulnerability Score of 16 (see the following article). This pitviper is found primarily at low elevations along the foothills of the Sierra Madre del Sur physiographic region and the coastal plain of the Planicie Costera del Pacífico and Planicie Costera de Tehuantepec physiographic regions (Mata-Silva et al., 2015b) in southern Oaxaca and extreme western Chiapas, Mexico. This individual was found ca. 3.6 km NNW of La Soledad, Municipio de Villa de Tututepec de Melchor Ocampo, Oaxaca. ' © Vicente Mata-Silva 543 www.mesoamericanherpetology.com www.eaglemountainpublishing.com The endemic herpetofauna of Mexico: organisms of global significance in severe peril JERRY D. JOHNSON1, LARRY DAVID WILSON2, VICENTE MATA-SILVA1, ELÍ GARCÍA-PADILLA3, AND DOMINIC L. DESANTIS1 1Department of Biological Sciences, The University of Texas at El Paso, El Paso, Texas 79968-0500, United States. E-mail: [email protected], and [email protected], and [email protected] 2Centro Zamorano de Biodiversidad, Escuela Agrícola Panamericana Zamorano, Departamento de Francisco Morazán, Honduras. E-mail: [email protected] 3Oaxaca de Juárez, Oaxaca 68023, Mexico. E-mail: [email protected] ABSTRACT: Life on Earth exists due to the interactions among the atmosphere, hydrosphere, and litho- sphere. Humans, however, have created and are faced with the consequences of an interrelated set of problems that impact all of these spheres, including the biosphere. The decline in the diversity of life is a problem of global dimensions resulting from a sixth mass extinction episode created by humans. -
A Statistical Assessment of Population Trends for Data Deficient Mexican Amphibians
A peer-reviewed version of this preprint was published in PeerJ on 16 December 2014. View the peer-reviewed version (peerj.com/articles/703), which is the preferred citable publication unless you specifically need to cite this preprint. Quintero E, Thessen AE, Arias-Caballero P, Ayala-Orozco B. 2014. A statistical assessment of population trends for data deficient Mexican amphibians. PeerJ 2:e703 https://doi.org/10.7717/peerj.703 A statistical assessment of population trends for data deficient Mexican amphibians Esther Quintero, Anne E. Thessen, Paulina Arias-Caballero, Bárbara Ayala-Orozco Background: Mexico is the fourth richest country in amphibians and the second country with the highest quantity of threatened amphibian species, and this number could be higher as many species are too poorly known to be accurately assigned to a risk category. The absence of a risk status or an unknown population trend can slow or halt conservation action, so it is vital to develop tools that in the absence of specific demographic data can assess a species’ risk of extinction, population trend, and to better understand which variables increase their vulnerability. Recent studies have demonstrated that the risk of species decline depends on extrinsic and intrinsic trait, thus including both of them for PrePrints assessing extinction might render more accurate assessment of threat. Methods: In this study harvested data from the Encyclopedia of Life (EOL) and the published literature for Mexican amphibians and used these data to assess the population trend of some of the Mexican species that have been assigned to the Data Deficient category of the IUCN using Random Forests, a Machine Learning method that gives a prediction of complex processes and identifies the most important variables that account for the predictions.