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Other Contributions
Other Contributions NATURE NOTES Amphibia: Caudata Ambystoma ordinarium. Predation by a Black-necked Gartersnake (Thamnophis cyrtopsis). The Michoacán Stream Salamander (Ambystoma ordinarium) is a facultatively paedomorphic ambystomatid species. Paedomorphic adults and larvae are found in montane streams, while metamorphic adults are terrestrial, remaining near natal streams (Ruiz-Martínez et al., 2014). Streams inhabited by this species are immersed in pine, pine-oak, and fir for- ests in the central part of the Trans-Mexican Volcanic Belt (Luna-Vega et al., 2007). All known localities where A. ordinarium has been recorded are situated between the vicinity of Lake Patzcuaro in the north-central portion of the state of Michoacan and Tianguistenco in the western part of the state of México (Ruiz-Martínez et al., 2014). This species is considered Endangered by the IUCN (IUCN, 2015), is protected by the government of Mexico, under the category Pr (special protection) (AmphibiaWeb; accessed 1April 2016), and Wilson et al. (2013) scored it at the upper end of the medium vulnerability level. Data available on the life history and biology of A. ordinarium is restricted to the species description (Taylor, 1940), distribution (Shaffer, 1984; Anderson and Worthington, 1971), diet composition (Alvarado-Díaz et al., 2002), phylogeny (Weisrock et al., 2006) and the effect of habitat quality on diet diversity (Ruiz-Martínez et al., 2014). We did not find predation records on this species in the literature, and in this note we present information on a predation attack on an adult neotenic A. ordinarium by a Thamnophis cyrtopsis. On 13 July 2010 at 1300 h, while conducting an ecological study of A. -
Herpetological Information Service No
Type Descriptions and Type Publications OF HoBART M. Smith, 1933 through June 1999 Ernest A. Liner Houma, Louisiana smithsonian herpetological information service no. 127 2000 SMITHSONIAN HERPETOLOGICAL INFORMATION SERVICE The SHIS series publishes and distributes translations, bibliographies, indices, and similar items judged useful to individuals interested in the biology of amphibians and reptiles, but unlikely to be published in the normal technical journals. Single copies are distributed free to interested individuals. Libraries, herpetological associations, and research laboratories are invited to exchange their publications with the Division of Amphibians and Reptiles. We wish to encourage individuals to share their bibliographies, translations, etc. with other herpetologists through the SHIS series. If you have such items please contact George Zug for instructions on preparation and submission. Contributors receive 50 free copies. Please address all requests for copies and inquiries to George Zug, Division of Amphibians and Reptiles, National Museum of Natural History, Smithsonian Institution, Washington DC 20560 USA. Please include a self-addressed mailing label with requests. Introduction Hobart M. Smith is one of herpetology's most prolific autiiors. As of 30 June 1999, he authored or co-authored 1367 publications covering a range of scholarly and popular papers dealing with such diverse subjects as taxonomy, life history, geographical distribution, checklists, nomenclatural problems, bibliographies, herpetological coins, anatomy, comparative anatomy textbooks, pet books, book reviews, abstracts, encyclopedia entries, prefaces and forwords as well as updating volumes being repnnted. The checklists of the herpetofauna of Mexico authored with Dr. Edward H. Taylor are legendary as is the Synopsis of the Herpetofalhva of Mexico coauthored with his late wife, Rozella B. -
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. -
DISCUSSION of the FLORA of GUADALUPE ISLAND Dr. Reid Moran1
DISCUSSION OF THE FLORA OF GUADALUPE ISLAND Dr. Reid Moran1: Guadalupe Island lies about 250 miles south- southwest of San Diego, California, and about 160 miles off the peninsula of Baja California, Mexico. Volcanic in origin and sep arated from the peninsula by depths of about 12,000 feet, it is clearly an oceanic island. Among the vascular plants recorded from Guadalupe Island and its islets, apparently 164 species are native. Goats, introduced more than a century ago, have eliminated some species and re duced others nearly to extinction. Outer Islet, a goatless refugium two miles south of the main island, has a native florula of 36 species. Nine of these (including Euphorbia misera and Lavatera occidentalis) are very scarce on the main island, largely confined to cliffs inaccessible to goats; another one (Coreopsis gigantea) has not been collected there since 1875; and five others (includ ing Lavatera lindsayi, Dudleya guadalupensis, and Rhus integri¬ folia) have never been recorded from there. Although it is not known that these five ever did occur on the main island, presum ably they did but were exterminated by the goats. These five, comprising 14 per cent of the native florula of Outer Islet, give the only suggestion we have as to how many species must have been eliminated from the main island by the goats before they could be found by botanists. Also reported from Guadalupe Island are 42 species that prob ably are not native. Several of these, each found only once, ap parently have not persisted; but, with the severe reduction of many native plants by the goats, other introduced plants have become abundant. -
Molecular Phylogeny of Atractus (Serpentes, Dipsadidae)
A peer-reviewed open-access journal ZooKeys 661: 91–123 (2017)Molecular phylogeny of Atractus (Serpentes, Dipsadidae)... 91 doi: 10.3897/zookeys.661.11224 RESEARCH ARTICLE http://zookeys.pensoft.net Launched to accelerate biodiversity research Molecular phylogeny of Atractus (Serpentes, Dipsadidae), with emphasis on Ecuadorian species and the description of three new taxa Alejandro Arteaga1, Konrad Mebert2, Jorge H. Valencia3, Diego F. Cisneros-Heredia4, Nicolás Peñafiel5, Carolina Reyes-Puig6, José L. Vieira-Fernandes1, Juan M. Guayasamin4,5 1 Tropical Herping, Av. 6 de Diciembre N31-50 y Whymper. Torres Santa Fe, Quito, Ecuador 2 Universidade Estadual de Santa Cruz, Departamento de Ciências Biológicas, Rodovia Jorge Amado, Km 16, 45662-900 Salobrinho, Ilhéus, Bahia, Brazil 3 Fundación Herpetológica Gustavo Orcés, Av. Amazonas 3008 y Calle Rumipamba, Casilla Postal 17-033-448, Quito, Ecuador 4 Universidad San Francisco de Quito (USFQ), Colegio de Ciencias Biológicas y Ambientales, Laboratorio de Biología Evolutiva, Laboratorio de Zoología Terrestre, campus Cumbayá, Casilla Postal 17-1200-841, Quito, Ecuador 5 Centro de Investigación de la Biodiversidad y Cambio Climático (BioCamb), Facultad de Ciencias de Medio Ambiente, Ingeniería en Biodi- versidad y Recursos Genéticos, Universidad Tecnológica Indoamérica, Av. Machala y Sabanilla, Quito, Ecuador 6 Museo Ecuatoriano de Ciencias Naturales, Instituto Nacional de Biodiversidad, División de Herpetología, calle Rumipamba 341 y Av. de los Shyris, Casilla 17-07-8976, Quito, Ecuador Corresponding author: Alejandro Arteaga ([email protected]) Academic editor: R. Jadin | Received 17 November 2016 | Accepted 8 March 2017 | Published 15 March 2017 http://zoobank.org/7CBF7FB1-EFEA-4DC1-8F64-5BF862694AA0 Citation: Arteaga A, Mebert K, Valencia JH, Cisneros-Heredia DF, Peñafiel N, Reyes-Puig C, Vieira-Fernandes JL, Guayasamin JM (2017) Molecular phylogeny of Atractus (Serpentes, Dipsadidae), with emphasis on Ecuadorian species and the description of three new taxa. -
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. -
Squamate Reptiles Challenge Paradigms of Genomic Repeat Element Evolution Set by Birds and Mammals
ARTICLE DOI: 10.1038/s41467-018-05279-1 OPEN Squamate reptiles challenge paradigms of genomic repeat element evolution set by birds and mammals Giulia I.M. Pasquesi1, Richard H. Adams1, Daren C. Card 1, Drew R. Schield1, Andrew B. Corbin1, Blair W. Perry1, Jacobo Reyes-Velasco1,2, Robert P. Ruggiero2, Michael W. Vandewege3, Jonathan A. Shortt4 & Todd A. Castoe1 1234567890():,; Broad paradigms of vertebrate genomic repeat element evolution have been largely shaped by analyses of mammalian and avian genomes. Here, based on analyses of genomes sequenced from over 60 squamate reptiles (lizards and snakes), we show that patterns of genomic repeat landscape evolution in squamates challenge such paradigms. Despite low variance in genome size, squamate genomes exhibit surprisingly high variation among spe- cies in abundance (ca. 25–73% of the genome) and composition of identifiable repeat ele- ments. We also demonstrate that snake genomes have experienced microsatellite seeding by transposable elements at a scale unparalleled among eukaryotes, leading to some snake genomes containing the highest microsatellite content of any known eukaryote. Our analyses of transposable element evolution across squamates also suggest that lineage-specific var- iation in mechanisms of transposable element activity and silencing, rather than variation in species-specific demography, may play a dominant role in driving variation in repeat element landscapes across squamate phylogeny. 1 Department of Biology, University of Texas at Arlington, 501S. Nedderman Drive, Arlington, TX 76019, USA. 2 Department of Biology, New York University Abu Dhabi, Saadiyat Island, United Arab Emirates. 3 Department of Biology, Institute for Genomics and Evolutionary Medicine, Temple University, Philadelphia, PA 19122, USA. -
Bulletin of the Essex Institute
THE NORTH AMERICAN REPTILES AND BATRACHIANS. A LIST OF THE SPECIES OCCURRING NORTH OF THE ISTHMUS OF TEHUANTEPEC, WITH REFERENCES. BY SAMUEL GARMAN. The following list is presented in the shape in which it has proved most useful in my own work. As in other pub- lications, I have placed the date immediately after the au- thority, as one naturally thinks it. In order accurately to determine species, comparison should be made with the original description rather than with the opinion of a sub- sequent writer ; for this reason reference is made to the discoverer and not to one in whose opinion the species belonofs to a o^enus some other than that in which it was originally placed. Consequently, the references are under names unaffected by frequent changes from one genus to another. Heretofore, the faunal limit for North America has been patriotically placed at the Mexican boundary. The distribution of the reptiles and Batrachians proves this limit to be unscientific, and shows the nearest approach to a separation between the faunae of the Americas, North and South, at the southern extremity of the tableland of Mexico. Attempt is made in this list to include all the species known to occur north of that point. When several localities for a species are given, they are chosen to indicate the extent of its range as nearly as possible. With a slight modification, the binomial system is fol- lowed. For various reasons, as will be seen below, the tri- (3) 4 garman's list op or polynomiiils affected by different authors, can hardly be considered improvements. -
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. -
The Conservation of Forest Genetic Resources Case Histories from Canada, Mexico, and the United States
The Conservation of Forest Genetic Resources Case Histories from Canada, Mexico, and the United States value of gene banks in the conservation of forest genetic resources. By E Thomas Ledig, J.JesusVargas-Hernandez, and Kurt H. Johnsen Prepared as a task of the Forest Genetic Resources Study Group/North American Forestry CornrnissioniFood and Agriculture Organization of the United Nations. Reprinted from the Joul-rzal of Forestry, Vol. 96, No. 1, January 1998. Not for further reproduction. e Conservation of Forest Case Histories from Canada, Mexico, and the United States he genetic codes of living organ- taken for granted: release of oxygen and isms are natural resources no less storage of carbon, amelioration of cli- T than soil, air, and water. Genetic mate, protection of watersheds, and resources-from nucleotide sequences others. Should genetic resources be lost, in DNA to selected genotypes, popula- ecosystem function may also be dam- tions, and species-are the raw mater- aged, usually expressed as a loss of pri- ial in forestry: for breeders, for the for- mary productivity, the rate at which a est manager who produces an eco- plant community stores energy and pro- nomic crop, for society that reaps the duces organic matter (e.g., Fetcher and environmental benefits provided by Shaver 1990). Losses in primary pro- forests, and for the continued evolu- ductivity result in changes in nutrient tion of the species itself. and gas cycling in Breeding, of course, The loss g~f;a ecosystems (Bormann requires genetic variation. and Likens 1979). Continued improvement p population is Genetic diversity is in medicines, agricultural the most basic element By F.