Trade in Non-Native Amphibians and Reptiles in Texas: Lessons for Better Monitoring and Implications for Species Introduction
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Birds, Reptiles, Amphibians, Vascular Plants, and Habitat in the Gila River Riparian Zone in Southwestern New Mexico
Birds, Reptiles, Amphibians, Vascular Plants, and Habitat in the Gila River Riparian Zone in Southwestern New Mexico Kansas Biological Survey Report #151 Kelly Kindscher, Randy Jennings, William Norris, and Roland Shook September 8, 2008 Birds, Reptiles, Amphibians, Vascular Plants, and Habitat in the Gila River Riparian Zone in Southwestern New Mexico Cover Photo: The Gila River in New Mexico. Photo by Kelly Kindscher, September 2006. Kelly Kindscher, Associate Scientist, Kansas Biological Survey, University of Kansas, 2101 Constant Avenue, Lawrence, KS 66047, Email: [email protected] Randy Jennings, Professor, Department of Natural Sciences, Western New Mexico University, PO Box 680, 1000 W. College Ave., Silver City, NM 88062, Email: [email protected] William Norris, Associate Professor, Department of Natural Sciences, Western New Mexico University, PO Box 680, 1000 W. College Ave., Silver City, NM 88062, Email: [email protected] Roland Shook, Emeritus Professor, Biology, Department of Natural Sciences, Western New Mexico University, PO Box 680, 1000 W. College Ave., Silver City, NM 88062, Email: [email protected] Citation: Kindscher, K., R. Jennings, W. Norris, and R. Shook. Birds, Reptiles, Amphibians, Vascular Plants, and Habitat in the Gila River Riparian Zone in Southwestern New Mexico. Open-File Report No. 151. Kansas Biological Survey, Lawrence, KS. ii + 42 pp. Abstract During 2006 and 2007 our research crews collected data on plants, vegetation, birds, reptiles, and amphibians at 49 sites along the Gila River in southwest New Mexico from upstream of the Gila Cliff Dwellings on the Middle and West Forks of the Gila to sites below the town of Red Rock, New Mexico. -
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. -
HERPETOLOGICAL BULLETIN Number 106 – Winter 2008
The HERPETOLOGICAL BULLETIN Number 106 – Winter 2008 PUBLISHED BY THE BRITISH HERPETOLOGICAL SOCIETY THE HERPETOLOGICAL BULLETIN Contents RESEA R CH AR TICLES Use of transponders in the post-release monitoring of translocated spiny-tailed lizards (Uromastyx aegyptia microlepis) in Abu Dhabi Emirate, United Arab Emirates Pritpal S. Soorae, Judith Howlett and Jamie Samour .......................... 1 Gastrointestinal helminths of three species of Dicrodon (Squamata: Teiidae) from Peru Stephen R. Goldberg and Charles R. Bursey ..................................... 4 Notes on the Natural History of the eublepharid Gecko Hemitheconyx caudicinctus in northwestern Ghana Stephen Spawls ........................................................ 7 Significant range extension for the Central American Colubrid snake Ninia pavimentata (Bocourt 1883) Josiah H. Townsend, J. Micheal Butler, Larry David Wilson, Lorraine P. Ketzler, John Slapcinsky and Nathaniel M. Stewart ..................................... 15 Predation on Italian Newt larva, Lissotriton italicus (Amphibia, Caudata, Salamandridae), by Agabus bipustulatus (Insecta, Coleoptera, Dytiscidae) Luigi Corsetti and Gianluca Nardi........................................ 18 Behaviour, Time Management, and Foraging Modes of a West Indian Racer, Alsophis sibonius Lauren A. White, Peter J. Muelleman, Robert W. Henderson and Robert Powell . 20 Communal egg-laying and nest-sites of the Goo-Eater, Sibynomorphus mikanii (Colubridae, Dipsadinae) in southeastern Brazil Henrique B. P. Braz, Francisco L. Franco -
Leopard Geckos & African Fat-Tails Geckos
A Compassionate Commitment to Quality Pet Care! LEOPARD GECKOS & AFRICAN FAT-TAILS GECKOS SPECIES NAMES Leopard geckos (Eublepharis maclarius), African fat-tailed geckos (Hemitheconyx caudicinctus). Both are members of the Eublepharidae family, which includes all species of geckos with moveable eyelids. CAGING/HOUSING For a single gecko, a 10-gallon glass aquarium with a securely fastened wire mesh top is appropriate. For two or more geckos a 20- gallon or larger aquarium is necessary. For substrate use paper towels, newspaper, or artificial turf, washed orchard bark, or aquarium gravel. The use of sand or calcium-fortified sand (such as ReptiSand™ or Calci-Sand™) is not recommended for geckos less than 6 inches in length, due to the risk of ingestion and subsequent impaction in the gastrointestinal tract. A hide-box, or shelter, should be provided to allow the gecko a quiet retreat. LIGHTING/HEATING In order to properly thermo-regulate, leopard geckos need a temperature gradient that allows them to move from a cooler end of the tank to a warmer end. This temperature gradient should range between 70°F at the cool end at 85°F at the high end. African fat-tailed geckos require slightly higher temperatures ranging from between 80°F and 92°F. Since these geckos are nocturnal, UV lighting is not necessary. HUMIDITY A moderate level of humidity is required for these geckos, which can be provided by misting and providing a large water bowl for the animal to soak in. Low humidity levels can lead to problems with shedding. FEEDING Food items, as a general rule, should be no longer than the length, and less than half the width of the geckos head. -
Temperature-Induced Colour Change Varies Seasonally in Bearded
applyparastyle "body/p[1]" parastyle "Text_First" Biological Journal of the Linnean Society, 2018, 123, 422–430. With 4 figures. Temperature-induced colour change varies seasonally in Downloaded from https://academic.oup.com/biolinnean/article-abstract/123/2/422/4774525 by University of Melbourne Library user on 01 November 2018 bearded dragon lizards VIVIANA CADENA,1* KATRINA RANKIN,1 KATHLEEN R. SMITH,1 JOHN A. ENDLER,2 and DEVI STUART-FOX1 1School of BioSciences, The University of Melbourne, Parkville, VIC 3010, Australia 2Centre for Integrative Ecology, School of Life and Environmental Sciences, Deakin University, Waurn Ponds, VIC 3220, Australia Received 14 September 2017; revised 17 November 2017; accepted for publication 18 November 2017 The benefits of colour change are expected to vary seasonally because of changes in reproductive activity, tem- perature and, potentially, predation risk; yet temporal variation in colour change has seldom been examined. We measured colour change in spring and autumn using captive individuals from two differently coloured populations of the central bearded dragon lizard, Pogona vitticeps. We predicted that colour change should be greater in spring than autumn because of the added requirements of reproductive and territorial activity. To elicit colour change in a standardized way, we placed lizards inside temperature-controlled chambers and measured colour at 15, 25, 35 and 40 °C, repeating experiments in spring and autumn. Lizards from both populations changed from dark grey to light yellowish or orange-brown (increasing luminance and saturation) with increasing temperature in both seasons, and both populations changed colour to a similar extent. As predicted, the maximal extent of temperature-induced colour change (in particular, luminance change) was greater in spring than autumn. -
Intelligence of Bearded Dragons Sydney Herndon
Murray State's Digital Commons Honors College Theses Honors College Spring 4-26-2021 Intelligence of Bearded Dragons sydney herndon Follow this and additional works at: https://digitalcommons.murraystate.edu/honorstheses Part of the Behavior and Behavior Mechanisms Commons Recommended Citation herndon, sydney, "Intelligence of Bearded Dragons" (2021). Honors College Theses. 67. https://digitalcommons.murraystate.edu/honorstheses/67 This Thesis is brought to you for free and open access by the Honors College at Murray State's Digital Commons. It has been accepted for inclusion in Honors College Theses by an authorized administrator of Murray State's Digital Commons. For more information, please contact [email protected]. Intelligence of Bearded Dragons Submitted in partial fulfillment of the requirements for the Murray State University Honors Diploma Sydney Herndon 04/2021 i Abstract The purpose of this thesis is to study and explain the intelligence of bearded dragons. Bearded dragons (Pogona spp.) are a species of reptile that have been popular in recent years as pets. Until recently, not much was known about their intelligence levels due to lack of appropriate research and studies on the species. Scientists have been studying the physical and social characteristics of bearded dragons to determine if they possess a higher intelligence than previously thought. One adaptation that makes bearded dragons unique is how they respond to heat. Bearded dragons optimize their metabolic functions through a narrow range of body temperatures that are maintained through thermoregulation. Many of their behaviors are temperature dependent, such as their speed when moving and their food response. When they are cold, these behaviors decrease due to their lower body temperature. -
Comparative Chromosome Painting and NOR Distribution Suggest a Complex Hybrid Origin of Triploid Lepidodactylus Lugubris (Gekkonidae)
RESEARCH ARTICLE Comparative Chromosome Painting and NOR Distribution Suggest a Complex Hybrid Origin of Triploid Lepidodactylus lugubris (Gekkonidae) Vladimir A. Trifonov1,2*, Alessio Paoletti3, Vincenzo Caputo Barucchi3,5, Tatiana Kalinina1,2, Patricia C. M. O’Brien4, Malcolm A. Ferguson-Smith4, Massimo Giovannotti3 1 Institute of Molecular and Cellular Biology SB RAS, Novosibirsk, Russia, 2 Novosibirsk State University, Novosibirsk, Russia, 3 Dipartimento di Scienze della Vita e dell’Ambiente, Università Politecnica delle Marche, Ancona, Italy, 4 Cambridge Resource Centre for Comparative Genomics, University of Cambridge, Cambridge, United Kingdom, 5 Consiglio Nazionale delle Ricerche, Istituto di Scienze Marine Sezione Pesca Marittima,Ancona, Italy * [email protected] OPEN ACCESS Citation: Trifonov VA, Paoletti A, Caputo Barucchi V, Abstract Kalinina T, O’Brien PCM, Ferguson-Smith MA, et al. (2015) Comparative Chromosome Painting and NOR Parthenogenesis, unisexuality and triploidy are interesting but poorly studied phenomena Distribution Suggest a Complex Hybrid Origin of Triploid Lepidodactylus lugubris (Gekkonidae). PLoS occurring in some reptile species. The mourning gecko (Lepidodactylus lugubris) repre- ONE 10(7): e0132380. doi:10.1371/journal. sents a complex of diploid and triploid parthenogenetic mostly all-female populations pone.0132380 (males occur quite rarely) widely distributed in coastal areas of the Indian and Pacific Editor: Roscoe Stanyon, University of Florence, Oceans. Here, we study karyotypes of a male and two female L. lugubris (LLU) triploid indi- ITALY viduals (3n = 66) using comparative painting with Gekko japonicus, Hemidactylus turcicus Received: October 10, 2014 and H. platyurus chromosome specific probes to visualize the homologous regions and to Accepted: June 13, 2015 reveal genus specific rearrangements. -
The Herpetofauna of the Cubango, Cuito, and Lower Cuando River Catchments of South-Eastern Angola
Official journal website: Amphibian & Reptile Conservation amphibian-reptile-conservation.org 10(2) [Special Section]: 6–36 (e126). The herpetofauna of the Cubango, Cuito, and lower Cuando river catchments of south-eastern Angola 1,2,*Werner Conradie, 2Roger Bills, and 1,3William R. Branch 1Port Elizabeth Museum (Bayworld), P.O. Box 13147, Humewood 6013, SOUTH AFRICA 2South African Institute for Aquatic Bio- diversity, P/Bag 1015, Grahamstown 6140, SOUTH AFRICA 3Research Associate, Department of Zoology, P O Box 77000, Nelson Mandela Metropolitan University, Port Elizabeth 6031, SOUTH AFRICA Abstract.—Angola’s herpetofauna has been neglected for many years, but recent surveys have revealed unknown diversity and a consequent increase in the number of species recorded for the country. Most historical Angola surveys focused on the north-eastern and south-western parts of the country, with the south-east, now comprising the Kuando-Kubango Province, neglected. To address this gap a series of rapid biodiversity surveys of the upper Cubango-Okavango basin were conducted from 2012‒2015. This report presents the results of these surveys, together with a herpetological checklist of current and historical records for the Angolan drainage of the Cubango, Cuito, and Cuando Rivers. In summary 111 species are known from the region, comprising 38 snakes, 32 lizards, five chelonians, a single crocodile and 34 amphibians. The Cubango is the most western catchment and has the greatest herpetofaunal diversity (54 species). This is a reflection of both its easier access, and thus greatest number of historical records, and also the greater habitat and topographical diversity associated with the rocky headwaters. -
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. -
Computational Molecular Species Delimitation and Taxonomic Revision of the Gecko Genus Ebenavia Boettger, 1878
The Science of Nature (2018) 105:49 https://doi.org/10.1007/s00114-018-1574-9 ORIGINAL PAPER Computational molecular species delimitation and taxonomic revision of the gecko genus Ebenavia Boettger, 1878 Oliver Hawlitschek1 & Mark D. Scherz1,2 & Bernhard Ruthensteiner1 & Angelica Crottini3 & Frank Glaw1 Received: 22 February 2018 /Revised: 13 June 2018 /Accepted: 3 July 2018 # Springer-Verlag GmbH Germany, part of Springer Nature 2018 Abstract Cryptic species have been detected in many groups of organisms and must be assumed to make up a significant portion of global biodiversity. We study geckos of the Ebenavia inunguis complex from Madagascar and surrounding islands and use species delimitation algorithms (GMYC, BOLD, BPP), COI barcode divergence, diagnostic codon indels in the nuclear marker PRLR, diagnostic categorical morphological characters, and significant differences in continuous morphological characters for its taxonomic revision. BPP yielded ≥ 10 operational taxonomic units, whereas GMYC (≥ 27) and BOLD (26) suggested substantial oversplitting. In consequnce, we resurrect Ebenavia boettgeri Boulenger 1885 and describe Ebenavia tuelinae sp. nov., Ebenavia safari sp. nov., and Ebenavia robusta sp. nov., increasing the number of recognised species in Ebenavia from two to six. Further lineages of Ebenavia retrieved by BPP may warrant species or subspecies status, but further taxonomic conclusions are postponed until more data become available. Finally, we present an identification key to the genus Ebenavia, provide an updated distribution map, and discuss the diagnostic values of computational species delimitation as well as morphological and molecular diagnostic characters. Keywords BOLD . Operational Taxonomic Unit . Madagascar clawless gecko . Integrative taxonomy . Taxonomic inflation . Species complex Introduction taxa (Bickford et al. -
Repeated Origin and Loss of Adhesive Toepads in Geckos
Marquette University e-Publications@Marquette Biological Sciences Faculty Research and Publications Biological Sciences, Department of 6-27-2012 Repeated Origin and Loss of Adhesive Toepads in Geckos Tony Gamble Eli Greenbaum Todd R. Jackman Anthony P. Russell Aaron M. Bauer Follow this and additional works at: https://epublications.marquette.edu/bio_fac Part of the Biology Commons Repeated Origin and Loss of Adhesive Toepads in Geckos Tony Gamble1,2, Eli Greenbaum3¤, Todd R. Jackman3, Anthony P. Russell4, Aaron M. Bauer3* 1 Department of Genetics, Cell Biology and Development, University of Minnesota, Minneapolis, Minnesota, United States of America, 2 Bell Museum of Natural History, University of Minnesota, St. Paul, Minnesota, United States of America, 3 Department of Biology, Villanova University, Villanova, Pennsylvania, United States of America, 4 Department of Biological Sciences, University Department of Calgary, Calgary, Canada Abstract Geckos are well known for their extraordinary clinging abilities and many species easily scale vertical or even inverted surfaces. This ability is enabled by a complex digital adhesive mechanism (adhesive toepads) that employs van der Waals based adhesion, augmented by frictional forces. Numerous morphological traits and behaviors have evolved to facilitate deployment of the adhesive mechanism, maximize adhesive force and enable release from the substrate. The complex digital morphologies that result allow geckos to interact with their environment in a novel fashion quite differently from most other lizards. Details of toepad morphology suggest multiple gains and losses of the adhesive mechanism, but lack of a comprehensive phylogeny has hindered efforts to determine how frequently adhesive toepads have been gained and lost. Here we present a multigene phylogeny of geckos, including 107 of 118 recognized genera, and determine that adhesive toepads have been gained and lost multiple times, and remarkably, with approximately equal frequency. -
0174 Lampropeltis Zonata.Pdf
174.1 REPTILIA: SQUAMATA: SERPENTES: COLUBRIDAE LAMPROPELTIS ZONATA Catalogue of American Amphibians and Reptiles. numerous publications (e.g. Blanchard, 1921; Bocourt, 1886; Ditmars, 1940; Dixon, 1967; Perkins, 1949; Schmidt and Davis, ZWEIFEL,RICHARDG. 1974. Lampropeltis zonata. 1941; Stebbins, 1954; Van Denburgh, 1897, 1922; Wright and Wright, 1957). Lampropeltis zonata (Lockington ex Blainville) • DISTRIBUTION.The main body of the range is from northern California Mountain Kingsnake Kern County, California, northward along the western flank of the Sierra Nevada into southwestern Oregon and southward in ? [Coluber] (Zacholus) zonatus Blainville, 1835:293. Type• the eastern part of the Coast Ranges (avoiding the moist locality, "Californie". Holotype formerly in Paris Museum, coastal region) to the area north of San Francisco Bay. South not now known to exist, collected by Paul Emile Botta. of San Francisco Bay, the species occurs in disjunct populations Bellophis zonatus Lockington, 1876:52. Type-locality, "Northern in the Coast, Transverse and Peninsular Ranges, terminating in California" (see remarks under L. z. zonata). Syntypes the Sierra San Pedro Martir of Baja California. A remarkably destroyed, formerly California Acad. Sci. 334, 335, collected isolated population is found on tiny South Todos Santos Island by "Paymaster Stanton, U.S.N." near Ensenada, Baja California. The species may be present Ophibolus triangulus var. zonatus: Garman, 1883:155 (but not on Santa Catalina Island off the coast of southern California, p. 67). New combination. as inferred from the following statement by Holder (1910: Ophibolus pyrrhomelas: Cope, 1892:610. Considers zonatus of 194): "Between Little Harbor and the Isthmus ... I saw a Lockington a synonym. beautiful coral snake with alternate rings of red and black." The Coronella zonata: Boulenger, 1894:202.