Ecology of the Eastern Collared Lizard, Crotaphytus Collaris, at Its Only Known Locality in Illinois Beth Burke Department of Zo
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Life History of the Coppertail Skink (Ctenotus Taeniolatus) in Southeastern Australia
Herpetological Conservation and Biology 15(2):409–415. Submitted: 11 February 2020; Accepted: 19 May 2020; Published: 31 August 2020. LIFE HISTORY OF THE COPPERTAIL SKINK (CTENOTUS TAENIOLATUS) IN SOUTHEASTERN AUSTRALIA DAVID A. PIKE1,2,6, ELIZABETH A. ROZNIK3, JONATHAN K. WEBB4, AND RICHARD SHINE1,5 1School of Biological Sciences A08, University of Sydney, New South Wales 2006, Australia 2Present address: Department of Biology, Rhodes College, Memphis, Tennessee 38112, USA 3Department of Conservation and Research, Memphis Zoo, Memphis, Tennessee 38112, USA 4School of Life Sciences, University of Technology Sydney, Broadway, New South Wales 2007, Australia 5Present address: Department of Biological Sciences, Macquarie University, New South Wales 2109, Australia 6Corresponding author, e-mail: [email protected] Abstract.—The global decline of reptiles is a serious problem, but we still know little about the life histories of most species, making it difficult to predict which species are most vulnerable to environmental change and why they may be vulnerable. Life history can help dictate resilience in the face of decline, and therefore understanding attributes such as sexual size dimorphism, site fidelity, and survival rates are essential. Australia is well-known for its diversity of scincid lizards, but we have little detailed knowledge of the life histories of individual scincid species. To examine the life history of the Coppertail Skink (Ctenotus taeniolatus), which uses scattered surface rocks as shelter, we estimated survival rates, growth rates, and age at maturity during a three-year capture-mark- recapture study. We captured mostly females (> 84%), and of individuals captured more than once, we captured 54.3% at least twice beneath the same rock, and of those, 64% were always beneath the same rock (up to five captures). -
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. -
The Functional Significance of Panting As a Mechanism of Thermoregulation and Its Relationship to the Critical Thermal Maxima in Lizards Caleb L
© 2020. Published by The Company of Biologists Ltd | Journal of Experimental Biology (2020) 223, jeb224139. doi:10.1242/jeb.224139 RESEARCH ARTICLE The functional significance of panting as a mechanism of thermoregulation and its relationship to the critical thermal maxima in lizards Caleb L. Loughran* and Blair O. Wolf* ABSTRACT lizards and its importance for thermoregulation have not been Because most desert-dwelling lizards rely primarily on behavioral widely investigated (Tattersall et al., 2006). thermoregulation for the maintenance of active body temperature, the Because lizards thermoregulate primarily by shuttling between effectiveness of panting as a thermoregulatory mechanism for different microclimates or by postural adjustments to maintain a evaporative cooling has not been widely explored. We measured preferred body temperature (Tpref ) before initiating open-mouthed panting, the onset of panting has historically been viewed as an changes in body temperature (Tb) with increasing air temperature (Ta) for 17 species of lizards that range across New Mexico and Arizona emergent response to unavoidable heat exposure and of approaching ’ and quantified the temperatures associated with the onset of panting, lethal Tb values near the animal s critical thermal maximum (CTmax; Weese, 1917; Cowles and Bogert, 1944; Dawson and Templeton, and the capacity of individuals to depress Tb below Ta while panting, 1966, Vernon and Heatwole, 1970; Webb et al., 1972, Tattersall and estimated the critical thermal maxima (CTmax) for each individual. -
PREDATION of the ENDANGERED BLUNT-NOSED LEOPARD LIZARD (GAMBELIA SILA) in the SAN JOAQUIN DESERT of CALIFORNIA Author: David J
PREDATION OF THE ENDANGERED BLUNT-NOSED LEOPARD LIZARD (GAMBELIA SILA) IN THE SAN JOAQUIN DESERT OF CALIFORNIA Author: David J. Germano Source: The Southwestern Naturalist, 63(4) : 276-280 Published By: Southwestern Association of Naturalists URL: https://doi.org/10.1894/0038-4909-63-4-276 BioOne Complete (complete.BioOne.org) is a full-text database of 200 subscribed and open-access titles in the biological, ecological, and environmental sciences published by nonprofit societies, associations, museums, institutions, and presses. Your use of this PDF, the BioOne Complete website, and all posted and associated content indicates your acceptance of BioOne’s Terms of Use, available at www.bioone.org/terms-of-use. Usage of BioOne Complete content is strictly limited to personal, educational, and non-commercial use. Commercial inquiries or rights and permissions requests should be directed to the individual publisher as copyright holder. BioOne sees sustainable scholarly publishing as an inherently collaborative enterprise connecting authors, nonprofit publishers, academic institutions, research libraries, and research funders in the common goal of maximizing access to critical research. Downloaded From: https://bioone.org/journals/The-Southwestern-Naturalist on 22 Oct 2019 Terms of Use: https://bioone.org/terms-of-use Access provided by Southwestern Association of Naturalists THE SOUTHWESTERN NATURALIST 63(4): 276–280 PREDATION OF THE ENDANGERED BLUNT-NOSED LEOPARD LIZARD (GAMBELIA SILA) IN THE SAN JOAQUIN DESERT OF CALIFORNIA DAVID J. GERMANO Department of Biology, California State University, Bakersfield, CA 93311-1099 Correspondent: [email protected] ABSTRACT—Predation can significantly affect prey populations, which could be significant for recovering species threatened with extinction. -
Crotaphytus Collaris
NEIGHBOR ASSESSME TAD THE DEAR E EMY PHENOMENON IN COLLARED LIZARDS, CROTAPHYTUS COLLARIS By JERRY F. HUSAK Bachelor of Science Angelo State University San Angelo, Texas 1998 Submitted to the Faculty of the Graduate College ofthe Oklahoma State Univer ity in partial fulfillment of the requirements for the degree of MASTER OF SCIENCE May, 2001 T SIS d: II ACKNOWLEDGMENTS I would like to thank many people for help during all stages of this project. I extend a great debt of gratitude to OG & E Electric Services, especially Mr. Bill Greene, for access to Sooner Lake Dam, especially on such short notice when this project began. I would like to thank the Rob and Bessie Welder Wildlife Foundation for partially funding this research. The Department ofZoology at Oklahoma State University has been very supportive, and I especially want to thank my committee members Dr. David Duvall and Dr. Charles Peterson for all oftheir ideas and comments. Dr. Troy Baird at the University of Central Oklahoma provided very helpful discussions about this project and helped iron out some of the wrinkles. I would like to thank Daren Riedle for helping me with fieldwork and making office time a little more entertaining. lowe a great deal to my advisor Dr. Stanley Fox, whose knowledge of lizard social behavior and behavioral ecology in general have been an inspiration to me. A special thanks goes to my mom and dad for being extremely supportive throughout my college years. Thanks to my sister Melissa for keeping me down to earth and to my brother Michael for inspiration and discussions about things biological. -
Animal Health Requirements for Importation of Reptiles, Amphibians, and Invertebrates Into Denmark
INTERNATIONAL TRADE DIVISION ANIMAL HEALTH REQUIREMENTS FOR IMPORTATION OF REPTILES, AMPHIBIANS, AND INVERTEBRATES INTO DENMARK. La 23,0-2100 These animal health requirements concern veterinary import requirements and certification re- quirements alone and shall apply without prejudice to other Danish and EU legislation. Reptiles, amphibians and invertebrates meaning animals of the Family/Species listed below (please note the exceptions): Order Family/Species Crocodilia Ostaeolaemus spp. (Dwarf Crocodile), Paleosuchus spp. (Cuvier's Dwarf Caiman and Smooth-fronted (Crocodiles) Caiman) and Alligator sinensis (Chinese alligator) Rhynchocephalia Sphenodontidae (Tuataras) Squamata (Liz- Corytophanidae, Iguanidae , Phrynosomatidae, Polychrotidae, Tropiduridae, Crotaphytidae, Opluridae, ards and snakes) Hoplocercidae, Agamidae, Chamaeleonidae, Gekkonidae, Pygopodidae, Dibamidae, Scincidae, Cordy- lidae, Gerrhosauridae, Xantusiidae, Lacertidae, Teiidae, Gymnophthalmidae, Anguidae, Anniellidae, Xenosauridae, Varanidae (except Varanus komodoensis, Varanus salvator, Varanus salvadoiri, Vara- nus niloticus and Varanus ornatus), Lanthanotidae, Helodermatidae, Aniliidae, Anomochilidae, Boidae (except Eunectes murinus) , Bolyeriidae, Cylindrophiidae , Loxocemidae , Pythonidae (except Python molurus, Python sebae and Python reticulatus), Tropidophiidae , Uropeltidae, Xenopeltidae, Anomalepididae, Leptotyphlopidae, Typhlopidae, Acrochordidae, Atractaspididae (except Atractaspis spp. and Macrelaps spp.), Colubridae (except Thelotornis spp., Dispholidus -
Habitat Use and Home Range of Long-Nosed Leopard Lizards (Gambelia Wislizenii) in Canyons of the Ancients National Monument, Colorado
Herpetological Conservation and Biology 6(2):312–323. Submitted: 2 March 2011; Accepted: 14 July 2011. HABITAT USE AND HOME RANGE OF LONG-NOSED LEOPARD LIZARDS (GAMBELIA WISLIZENII) IN CANYONS OF THE ANCIENTS NATIONAL MONUMENT, COLORADO 1,3 1 2 ROBERT A. SCHORR , BRAD A. LAMBERT , AND ERIC FREELS 1Colorado Natural Heritage Program, Colorado State University, Fort Collins, Colorado 80523, USA 2Dolores Public Lands Office, San Juan Public Lands, 100 North Sixth Street, Box 210, Dolores, Colorado 81323, USA 3Corresponding author, e-mail: [email protected] Abstract.—An understanding of species’ habitat requirements is needed for effective land management decisions, but for many North American reptiles, habitat use information is lacking. Gambelia wislizenii (Long-nosed Leopard Lizard) is a predatory lizard of most North American deserts, and, although common in the interior of its range, appears to be declining at some peripheral populations. To understand habitat use and movement patterns, we used telemetry and two habitat comparison methods to study a G. wislizenii population at the eastern boundary of the range. Gambelia wislizenii home ranges at Canyons of the Ancients National Monument, Colorado, are the largest recorded. Habitat analysis using microsite-attribute comparisons and compositional analysis documented second-order habitat preference for Big Sagebrush- or Utah Juniper-dominated landscapes. Gambelia wislizenii were found in areas with moderate shrub and forb cover with much bare ground, but were not found in areas dominated with grass cover. Incorporating management strategies that limit grass encroachment and maintain bare ground cover with moderate tree and shrub cover may help sustain G. wislizenii populations. -
Life History Account for Long-Nosed Leopard Lizard
California Wildlife Habitat Relationships System California Department of Fish and Wildlife California Interagency Wildlife Task Group LONG-NOSED LEOPARD LIZARD Gambelia wislizenii Family: CROTAPHYTIDAE Order: SQUAMATA Class: REPTILIA R018 Written by: R. Marlow Reviewed by: T. Papenfuss Edited by: S. Granholm Updated by: CWHR Program Staff, March 2000 DISTRIBUTION, ABUNDANCE, AND SEASONALITY The long-nosed leopard lizard is widely distributed in the Southeastern Great Basin, Mojave, Sonoran and Colorado deserts of California and at the southern end of the Central Valley in Santa Barbara and eastern Kern cos. Frequents a variety of desert woodland and scrub habitats up to 1830 m (6000 ft) (Stebbins 1985). Prefers sandy or gravelly flats and plains, and is less common in rocky areas. The greatest densities have been observed in creosote flats. Becomes active later in the spring than do other lizards, usually not until mid-April, and is not found after mid-August (Stebbins 1954, McCoy 1967, Montanucci 1967, Parker and Pianka 1976, Tollestrup 1979, 1983). SPECIFIC HABITAT REQUIREMENTS Feeding: This lizard eats insects (grasshoppers, beetles, etc.), lizards (Callisaurus, Cnemidophorus, Phrynosoma, etc.) and occasionally some plant material (Stebbins 1954, Dixon 1967, Tollestrup 1979). Cover: This species excavates its own burrows in sandy and friable soils and probably uses rodent burrows. Reproduction: This lizard requires adequate food supplies for reproduction. Water: Not required. Pattern: This lizard occupies desert flats and woodlands with sandy or gravelly substrates. SPECIES LIFE HISTORY Activity Patterns: Adults are active from mid-April to mid-August. This lizard is diurnal and can be active all day when the weather is mild to warm. -
[email protected] Biodiversity @Maddreptiles
Timothy Colston Biological Science Harnessing NGS Technologies to Understand Biological Diversification: From Microbes to Macroevolutionary Patterns [email protected] Biodiversity @maddreptiles Source: International Conference on Biodiversity Motivation & Tools –Molecular [email protected] @maddreptiles (NGS) [email protected] Biodiversity @maddreptiles Source: International Conference on Biodiversity [email protected] Biodiversity @maddreptiles [email protected] Biodiversity –the “microbiome” @maddreptiles NGS Sequencing [email protected] Biodiversity –the “microbiome” @maddreptiles NGS Sequencing [email protected] Biodiversity –the “microbiome” @maddreptiles • Plants and Animals are “metagenomic organisms” – Co‐evolution • Host‐associated microbial cells ~ 10X number of host cells – Fitness/Selection – Heritable by Gaby D'Allesandro / © AMNH [email protected] Biodiversity –the “microbiome” @maddreptiles • Plants and Animals are “metagenomic organisms” – Co‐evolution • Host‐associated microbial genes > 10X number of host cells – Fitness/Selection – Heritable by Gaby D'Allesandro / © AMNH [email protected] Biodiversity –the “microbiome” @maddreptiles Mammals Fish Birds Amphibians Reptiles Colston, T.J. & Jackson, C.R. (2016) Molecular Ecology The Reptile Microbiome C h a m A a g e a A l m e m V o L i a p d n a h a i r H d a n i s e e L t T a n b h S l a r a i A o e A d o a c h X e d n g n a n e i n D e T e o n g r e o n i n t n r r a d i u i L t i s m o o e d o c i a e i d a p p a l s t d e i a y l h o i e a u d a i a l d t C c i B o r u -
California Wildlife Habitat Relationships System California Department of Fish and Wildlife California Interagency Wildlife Task Group
California Wildlife Habitat Relationships System California Department of Fish and Wildlife California Interagency Wildlife Task Group BAJA CALIFORNIA COLLARED LIZARD Crotaphytus vestigium Family: CROTAPHYTIDAE Order: SQUAMATA Class: REPTILIA R093 Written by: T. Kucera, 1998 Updated by: CWHR Staff, February 2008 DISTRIBUTION, ABUNDANCE, AND SEASONALITY The Baja California collared lizard inhabits the eastern face of the peninsular ranges and adjacent rocky slopes from the northern slope of the San Jacinto mountains to the Mexican border and south into Baja California, Mexico (Sanborn and Loomis 1979, McGuire 1996). It is generally restricted to rocky outcroppings on more rugged portions of alluvial fans, desert hillsides, canyons, and lava flows. It is most common in xeric, rocky areas with little vegetation, including desert succulent shrub, desert scrub, and desert wash habitats. Little has been written about its natural history. The Baja California collared lizard is active in the spring and summer and to a lesser extent in the fall. SPECIFIC HABITAT REQUIREMENTS Feeding: Little is known of the diet of this species. The diet of the closely related Mojave black- collared lizard (C. bicinctores) consists largely of arthropods and small vertebrates (Stebbins 1985, McGuire 1996). Plant material is also occasionally consumed. Cover: This species prefers rocky areas and seeks cover under rocks and in cracks and crevices and rodent holes (Stebbins 1985), occasionally bounding bipedally from stone to stone when disturbed (McGuire 1996). Reproduction: Little is known about the reproductive requirements of this species. The closely related Mojave black-collared lizard lays eggs and presumably constructs its own nest but there are no reports. -
Pdf> (Accessed of Life
Molecular Phylogenetics and Evolution 94 (2016) 537–547 Contents lists available at ScienceDirect Molecular Phylogenetics and Evolution journal homepage: www.elsevier.com/locate/ympev Combining phylogenomic and supermatrix approaches, and a time-calibrated phylogeny for squamate reptiles (lizards and snakes) based on 52 genes and 4162 species q ⇑ Yuchi Zheng a,b, John J. Wiens b, a Department of Herpetology, Chengdu Institute of Biology, Chinese Academy of Sciences, Chengdu 610041, China b Department of Ecology and Evolutionary Biology, University of Arizona, Tucson, AZ 85721-088, USA article info abstract Article history: Two common approaches for estimating phylogenies in species-rich groups are to: (i) sample many loci Received 26 May 2015 for few species (e.g. phylogenomic approach), or (ii) sample many species for fewer loci (e.g. supermatrix Revised 30 September 2015 approach). In theory, these approaches can be combined to simultaneously resolve both higher-level rela- Accepted 8 October 2015 tionships (with many genes) and species-level relationships (with many taxa). However, fundamental Available online 22 October 2015 questions remain unanswered about this combined approach. First, will higher-level relationships more closely resemble those estimated from many genes or those from many taxa? Second, will branch sup- Keywords: port increase for higher-level relationships (relative to the estimate from many taxa)? Here, we address Missing data these questions in squamate reptiles. We combined two recently published datasets, one based on 44 Phylogenomic Phylogeny genes for 161 species, and one based on 12 genes for 4161 species. The likelihood-based tree from the Squamata combined matrix (52 genes, 4162 species) shared more higher-level clades with the 44-gene tree (90% Supermatrix vs. -
Impacts of Off-Highway Motorized Vehicles on Sensitive Reptile Species in Owyhee County, Idaho
Impacts of Off-Highway Motorized Vehicles on Sensitive Reptile Species in Owyhee County, Idaho by James C. Munger and Aaron A. Ames Department of Biology Boise State University, Boise, ID 83725 Final Report of Research Funded by a Cost-share Agreement between Boise State University and the Bureau of Land Management June 1998 INTRODUCTION As the population of southwestern Idaho grows, there is a corresponding increase in the number of recreational users of off-highway motorized vehicles (OHMVs). An extensive trail system has evolved in the Owyhee Front, and several off-highway motorized vehicle races are proposed for any given year. Management decisions by the Bureau of Land Management (BLM) regarding the use of public lands for OHMV activity should take account of the impact of OHMV activity on wildlife habitat and populations. However, our knowledge of the impact of this increased activity on many species of native wildlife is minimal. Of particular interest is the herpetofauna of the area: the Owyhee Front includes the greatest diversity of reptile species of any place in Idaho, and includes nine lizard species and ten snake species (Table 1). Three of these species are considered to be "sensitive" by BLM and Idaho Department of Fish and Game (IDFG): Sonora semiannulata (western ground snake), Rhinocheilus lecontei (long-nosed snake), and Crotaphytus bicinctores (Mojave black-collared lizard). One species, Hypsiglena torquata (night snake), was recently removed from the sensitive list, but will be regarded as "sensitive" for the purposes of this report. Off-highway motorized vehicles could impact reptiles in several ways. First, they may run over and kill individuals.