Check List LISTS of SPECIES Check List 11(3): 1642, April 2015 Doi: ISSN 1809-127X © 2015 Check List and Authors
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CAT Vertebradosgt CDC CECON USAC 2019
Catálogo de Autoridades Taxonómicas de vertebrados de Guatemala CDC-CECON-USAC 2019 Centro de Datos para la Conservación (CDC) Centro de Estudios Conservacionistas (Cecon) Facultad de Ciencias Químicas y Farmacia Universidad de San Carlos de Guatemala Este documento fue elaborado por el Centro de Datos para la Conservación (CDC) del Centro de Estudios Conservacionistas (Cecon) de la Facultad de Ciencias Químicas y Farmacia de la Universidad de San Carlos de Guatemala. Guatemala, 2019 Textos y edición: Manolo J. García. Zoólogo CDC Primera edición, 2019 Centro de Estudios Conservacionistas (Cecon) de la Facultad de Ciencias Químicas y Farmacia de la Universidad de San Carlos de Guatemala ISBN: 978-9929-570-19-1 Cita sugerida: Centro de Estudios Conservacionistas [Cecon]. (2019). Catálogo de autoridades taxonómicas de vertebrados de Guatemala (Documento técnico). Guatemala: Centro de Datos para la Conservación [CDC], Centro de Estudios Conservacionistas [Cecon], Facultad de Ciencias Químicas y Farmacia, Universidad de San Carlos de Guatemala [Usac]. Índice 1. Presentación ............................................................................................ 4 2. Directrices generales para uso del CAT .............................................. 5 2.1 El grupo objetivo ..................................................................... 5 2.2 Categorías taxonómicas ......................................................... 5 2.3 Nombre de autoridades .......................................................... 5 2.4 Estatus taxonómico -
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. -
Aquiloeurycea Scandens (Walker, 1955). the Tamaulipan False Brook Salamander Is Endemic to Mexico
Aquiloeurycea scandens (Walker, 1955). The Tamaulipan False Brook Salamander is endemic to Mexico. Originally described from caves in the Reserva de la Biósfera El Cielo in southwestern Tamaulipas, this species later was reported from a locality in San Luis Potosí (Johnson et al., 1978) and another in Coahuila (Lemos-Espinal and Smith, 2007). Frost (2015) noted, however, that specimens from areas remote from the type locality might be unnamed species. This individual was found in an ecotone of cloud forest and pine-oak forest near Ejido La Gloria, in the municipality of Gómez Farías. Wilson et al. (2013b) determined its EVS as 17, placing it in the middle portion of the high vulnerability category. Its conservation status has been assessed as Vulnerable by IUCN, and as a species of special protection by SEMARNAT. ' © Elí García-Padilla 42 www.mesoamericanherpetology.com www.eaglemountainpublishing.com The herpetofauna of Tamaulipas, Mexico: composition, distribution, and conservation status SERGIO A. TERÁN-JUÁREZ1, ELÍ GARCÍA-PADILLA2, VICENTE Mata-SILva3, JERRY D. JOHNSON3, AND LARRY DavID WILSON4 1División de Estudios de Posgrado e Investigación, Instituto Tecnológico de Ciudad Victoria, Boulevard Emilio Portes Gil No. 1301 Pte. Apartado postal 175, 87010, Ciudad Victoria, Tamaulipas, Mexico. Email: [email protected] 2Oaxaca de Juárez, Oaxaca, Código Postal 68023, Mexico. E-mail: [email protected] 3Department of Biological Sciences, The University of Texas at El Paso, El Paso, Texas 79968-0500, United States. E-mails: [email protected] and [email protected] 4Centro Zamorano de Biodiversidad, Escuela Agrícola Panamericana Zamorano, Departamento de Francisco Morazán, Honduras. E-mail: [email protected] ABSTRACT: The herpetofauna of Tamaulipas, the northeasternmost state in Mexico, is comprised of 184 species, including 31 anurans, 13 salamanders, one crocodylian, 124 squamates, and 15 turtles. -
A Review of the Cnemidophorus Lemniscatus Group in Central America (Squamata: Teiidae), with Comments on Other Species in the Group
TERMS OF USE This pdf is provided by Magnolia Press for private/research use. Commercial sale or deposition in a public library or website is prohibited. Zootaxa 3722 (3): 301–316 ISSN 1175-5326 (print edition) www.mapress.com/zootaxa/ Article ZOOTAXA Copyright © 2013 Magnolia Press ISSN 1175-5334 (online edition) http://dx.doi.org/10.11646/zootaxa.3722.3.1 http://zoobank.org/urn:lsid:zoobank.org:pub:4E9BA052-EEA9-4262-8DDA-E1145B9FA996 A review of the Cnemidophorus lemniscatus group in Central America (Squamata: Teiidae), with comments on other species in the group JAMES R. MCCRANIE1,3 & S. BLAIR HEDGES2 110770 SW 164th Street, Miami, Florida 33157-2933, USA. E-mail: [email protected] 2Department of Biology, 208 Mueller Laboratory, Pennsylvania State University, University Park, Pennsylvania 16802-5301, USA. E-mail: [email protected] 3Corresponding author. E-mail: [email protected] Abstract We provide the results of a morphological and molecular study on the Honduran Bay Island and mainland populations of the Cnemidophorus lemniscatus complex for which we resurrect C. ruatanus comb. nov. as a full species. Morphological comparison of the Honduran populations to Cnemidophorus populations from Panama led to the conclusion that the Pan- amanian population represents an undescribed species named herein. In light of these new results, and considering past morphological studies of several South American populations of the C. lemniscatus group, we suggest that three other nominal forms of the group are best treated as valid species: C. espeuti (described as a full species, but subsequently treat- ed as a synonym of C. lemniscatus or a subspecies of C. -
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. -
Other Contributions
Other Contributions NATURE NOTES Amphibia: Anura Family Bufonidae Incilius marmoreus (Wiegmann, 1833). Reproduction. The distribution of the Marbled Toad, Incilius marmo- reus, a Mexican endemic, extends from northern Sinaloa to Chiapas along the Pacific coastal plain, with an isolated population in Veracruz (Frost, 2017); on the Atlantic versant, Lemos Espinal and Dixon (2016: 354) also noted that this species occurs from “northern Hidalgo to the Isthmus of Tehuantepec.” Hardy and McDiarmid (1969) reported that most individuals in Sinaloa were found on the road at night during or just after rains, and that most females were collected in July and contained eggs. In Hidalgo, I. marmoreus aggregates in temporary ponds during the rainy season (Lemos Espinal and Dixon, 2016). Herein, I present data from a histological examination of I. marmoreus gonadal material from Colima and Sinaloa, and provide the minimum sizes for reproductive activity in males and females. The use of museum collections for obtaining reproductive data avoids removing additional animals from the wild. I examined 42 specimens of I. marmoreus (11 from Colima, collected in 1967, and 31 from Sinaloa, collected in 1960, 1962, 1963, and 1968). The combined samples consisted of 17 males (mean snout–vent length [SVL] = 54.5 mm ± 3.1 SD, range = 48–58 mm), 21 females (mean SVL = 60.9 mm ± 4.5 SD, range = 54–70 mm) and four juveniles from Sinaloa (mean SVL = 38.4 mm ± 7.1 SD, range = 29–44 mm); the specimens are maintained in the herpetology collection of the Natural History Museum of Los Angeles County (LACM), Los Angeles, California, United States (Appendix 1). -
Multi-National Conservation of Alligator Lizards
MULTI-NATIONAL CONSERVATION OF ALLIGATOR LIZARDS: APPLIED SOCIOECOLOGICAL LESSONS FROM A FLAGSHIP GROUP by ADAM G. CLAUSE (Under the Direction of John Maerz) ABSTRACT The Anthropocene is defined by unprecedented human influence on the biosphere. Integrative conservation recognizes this inextricable coupling of human and natural systems, and mobilizes multiple epistemologies to seek equitable, enduring solutions to complex socioecological issues. Although a central motivation of global conservation practice is to protect at-risk species, such organisms may be the subject of competing social perspectives that can impede robust interventions. Furthermore, imperiled species are often chronically understudied, which prevents the immediate application of data-driven quantitative modeling approaches in conservation decision making. Instead, real-world management goals are regularly prioritized on the basis of expert opinion. Here, I explore how an organismal natural history perspective, when grounded in a critique of established human judgements, can help resolve socioecological conflicts and contextualize perceived threats related to threatened species conservation and policy development. To achieve this, I leverage a multi-national system anchored by a diverse, enigmatic, and often endangered New World clade: alligator lizards. Using a threat analysis and status assessment, I show that one recent petition to list a California alligator lizard, Elgaria panamintina, under the US Endangered Species Act often contradicts the best available science. -
Herpetological Review
Herpetological Review Volume 41, Number 2 — June 2010 SSAR Offi cers (2010) HERPETOLOGICAL REVIEW President The Quarterly News-Journal of the Society for the Study of Amphibians and Reptiles BRIAN CROTHER Department of Biological Sciences Editor Southeastern Louisiana University ROBERT W. HANSEN Hammond, Louisiana 70402, USA 16333 Deer Path Lane e-mail: [email protected] Clovis, California 93619-9735, USA [email protected] President-elect JOSEPH MENDLELSON, III Zoo Atlanta, 800 Cherokee Avenue, SE Associate Editors Atlanta, Georgia 30315, USA e-mail: [email protected] ROBERT E. ESPINOZA KERRY GRIFFIS-KYLE DEANNA H. OLSON California State University, Northridge Texas Tech University USDA Forestry Science Lab Secretary MARION R. PREEST ROBERT N. REED MICHAEL S. GRACE PETER V. LINDEMAN USGS Fort Collins Science Center Florida Institute of Technology Edinboro University Joint Science Department The Claremont Colleges EMILY N. TAYLOR GUNTHER KÖHLER JESSE L. BRUNNER Claremont, California 91711, USA California Polytechnic State University Forschungsinstitut und State University of New York at e-mail: [email protected] Naturmuseum Senckenberg Syracuse MICHAEL F. BENARD Treasurer Case Western Reserve University KIRSTEN E. NICHOLSON Department of Biology, Brooks 217 Section Editors Central Michigan University Mt. Pleasant, Michigan 48859, USA Book Reviews Current Research Current Research e-mail: [email protected] AARON M. BAUER JOSHUA M. HALE BEN LOWE Department of Biology Department of Sciences Department of EEB Publications Secretary Villanova University MuseumVictoria, GPO Box 666 University of Minnesota BRECK BARTHOLOMEW Villanova, Pennsylvania 19085, USA Melbourne, Victoria 3001, Australia St Paul, Minnesota 55108, USA P.O. Box 58517 [email protected] [email protected] [email protected] Salt Lake City, Utah 84158, USA e-mail: [email protected] Geographic Distribution Geographic Distribution Geographic Distribution Immediate Past President ALAN M. -
The Impact of Climate Change Measured at Relevant Spatial Scales: New Hope for Tropical Lizards
Global Change Biology (2013) 19, 3093–3102, doi: 10.1111/gcb.12253 The impact of climate change measured at relevant spatial scales: new hope for tropical lizards MICHAEL L. LOGAN*, RYAN K. HUYNH† ,RACHELA.PRECIOUS‡ and RYAN G. CALSBEEK* *Department of Biology, Dartmouth College, 78 College St., Hanover, NH 03755, USA, †Department of Ecology and Evolutionary Biology, Princeton University, 106 Guyot Hall, Princeton, NJ 08544, USA, ‡Department of Natural Resource Conservation, University of Massachusetts-Amherst, 160 Holdsworth Way, Amherst, MA 01003, USA Abstract Much attention has been given to recent predictions that widespread extinctions of tropical ectotherms, and tropical forest lizards in particular, will result from anthropogenic climate change. Most of these predictions, however, are based on environmental temperature data measured at a maximum resolution of 1 km2, whereas individuals of most species experience thermal variation on a much finer scale. To address this disconnect, we combined thermal perfor- mance curves for five populations of Anolis lizard from the Bay Islands of Honduras with high-resolution tempera- ture distributions generated from physical models. Previous research has suggested that open-habitat species are likely to invade forest habitat and drive forest species to extinction. We test this hypothesis, and compare the vulnera- bilities of closely related, but allopatric, forest species. Our data suggest that the open-habitat populations we studied will not invade forest habitat and may actually benefit from predicted warming for many decades. Conversely, one of the forest species we studied should experience reduced activity time as a result of warming, while two others are unlikely to experience a significant decline in performance. -
THE ORIGIN and EVOLUTION of SNAKE EYES Dissertation
CONQUERING THE COLD SHUDDER: THE ORIGIN AND EVOLUTION OF SNAKE EYES Dissertation Presented in Partial Fulfillment for the Requirements for the Degree of Doctor of Philosophy in the Graduate School of The Ohio State University By Christopher L. Caprette, B.S., M.S. **** The Ohio State University 2005 Dissertation Committee: Thomas E. Hetherington, Advisor Approved by Jerry F. Downhower David L. Stetson Advisor The graduate program in Evolution, John W. Wenzel Ecology, and Organismal Biology ABSTRACT I investigated the ecological origin and diversity of snakes by examining one complex structure, the eye. First, using light and transmission electron microscopy, I contrasted the anatomy of the eyes of diurnal northern pine snakes and nocturnal brown treesnakes. While brown treesnakes have eyes of similar size for their snout-vent length as northern pine snakes, their lenses are an average of 27% larger (Mann-Whitney U test, p = 0.042). Based upon the differences in the size and position of the lens relative to the retina in these two species, I estimate that the image projected will be smaller and brighter for brown treesnakes. Northern pine snakes have a simplex, all-cone retina, in keeping with a primarily diurnal animal, while brown treesnake retinas have mostly rods with a few, scattered cones. I found microdroplets in the cone ellipsoids of northern pine snakes. In pine snakes, these droplets act as light guides. I also found microdroplets in brown treesnake rods, although these were less densely distributed and their function is unknown. Based upon the density of photoreceptors and neural layers in their retinas, and the predicted image size, brown treesnakes probably have the same visual acuity under nocturnal conditions that northern pine snakes experience under diurnal conditions. -
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. Amphib. Reptile Conserv. | http://redlist-ARC.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. -
Redalyc.Comparative Studies of Supraocular Lepidosis in Squamata
Multequina ISSN: 0327-9375 [email protected] Instituto Argentino de Investigaciones de las Zonas Áridas Argentina Cei, José M. Comparative studies of supraocular lepidosis in squamata (reptilia) and its relationships with an evolutionary taxonomy Multequina, núm. 16, 2007, pp. 1-52 Instituto Argentino de Investigaciones de las Zonas Áridas Mendoza, Argentina Disponible en: http://www.redalyc.org/articulo.oa?id=42801601 Cómo citar el artículo Número completo Sistema de Información Científica Más información del artículo Red de Revistas Científicas de América Latina, el Caribe, España y Portugal Página de la revista en redalyc.org Proyecto académico sin fines de lucro, desarrollado bajo la iniciativa de acceso abierto ISSN 0327-9375 COMPARATIVE STUDIES OF SUPRAOCULAR LEPIDOSIS IN SQUAMATA (REPTILIA) AND ITS RELATIONSHIPS WITH AN EVOLUTIONARY TAXONOMY ESTUDIOS COMPARATIVOS DE LA LEPIDOSIS SUPRA-OCULAR EN SQUAMATA (REPTILIA) Y SU RELACIÓN CON LA TAXONOMÍA EVOLUCIONARIA JOSÉ M. CEI † las subfamilias Leiosaurinae y RESUMEN Enyaliinae. Siempre en Iguania Observaciones morfológicas Pleurodonta se evidencian ejemplos previas sobre un gran número de como los inconfundibles patrones de especies permiten establecer una escamas supraoculares de correspondencia entre la Opluridae, Leucocephalidae, peculiaridad de los patrones Polychrotidae, Tropiduridae. A nivel sistemáticos de las escamas específico la interdependencia en supraoculares de Squamata y la Iguanidae de los géneros Iguana, posición evolutiva de cada taxón Cercosaura, Brachylophus,