Opportunistically Collected UV Exposure Data for Some Lizards in Cuba and Grand Cayman
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A New Subspecies of Anolis Porcatus (Sauna: Polychrotidae) from Western Cuba
Rev. Biol. Trop., 44(3)/45(1): 295-299, 1996-1997 A new subspecies of Anolis porcatus (Sauna: Polychrotidae) from Western Cuba O. Pérez-Beato 6780 W 2nd Ct. Apt. 212, Hialeah, Florida 33012, U.S.A. (Rec. l-IX-1995. Rev. ll-IX-1995. Acep. 22-11-1996) Abstract: A new subspecies of Anolis porcatus Gray, is described fromwestem Cuba. The main characters differenti ating Anolis porcattis aracelyae are a Iight blúe tint dorsum and an elongated ear opening. The distribution of the new taxon may be explained on the basis of allopatry in the Guaniguanico mountain range. Key words: Anolis porcatus, Cuba, Polychrotidae , subspecies Since the original description of Anolis por examined 325 additional specimens from popu catus (Gray 1840), this species was twice con lations throughout Cuba; unfortunately, sorne sidered a subspecies of Anolis carolinensis of tbis have been lost. Duméril and Bibron (Barbour 1937, Oliver The presence of a peculiar phenotype with a 1948), although Gray's allocation generally has light blue color in adult males and with an prevailed. The most complete systematic treat elongated ear opening in both sexes became ment was by Ruibal and Williams (1961). They evident in samples from western Cuba. This described the variability observed among and variation in ear shape had been noted by Ruibal between populations of A. porcatus across and Williams (1961) for Pinar de Río popula Cuba and proposed not fewer than four tions. The distribution of this phenotype hypotheses to explain the possible existence of ineludes almost the entire province of Pinar del several species and subspecies. -
Cfreptiles & Amphibians
HTTPS://JOURNALS.KU.EDU/REPTILESANDAMPHIBIANSTABLE OF CONTENTS IRCF REPTILES & AMPHIBIANSREPTILES • VOL15, & N AMPHIBIANSO 4 • DEC 2008 •189 28(1):44–46 • APR 2021 IRCF REPTILES & AMPHIBIANS CONSERVATION AND NATURAL HISTORY TABLE OF CONTENTS CubanFEATURE ARTICLES Green Anoles (Anolis porcatus): . Chasing Bullsnakes (Pituophis catenifer sayi) in Wisconsin: CommunalOn the Road to Understanding the Ecology Nestingand Conservation of the Midwest’s in Giant SerpentBromeliads ...................... Joshua M. Kapfer 190 . The Shared History of Treeboas (Corallus grenadensis) and Humans on Grenada: A Hypothetical Excursion ............................................................................................................................Robert W. Henderson 198 L. Yusnaviel García-Padrón RESEARCH ARTICLES Sociedad Espeleológica de Cuba, La Habana, Cuba; Sociedad Cubana de Zoología, La Habana 12000, Cuba ([email protected]) . The Texas Horned Lizard in Central and Western TexasPhotographs ....................... by the Emily author. Henry, Jason Brewer, Krista Mougey, and Gad Perry 204 . The Knight Anole (Anolis equestris) in Florida .............................................Brian J. Camposano, Kenneth L. Krysko, Kevin M. Enge, Ellen M. Donlan, and Michael Granatosky 212 CONSERVATION ALERT noles (Anolis spp.) lay single eggs buried in soil, under (22º32'20"N, 83º50'04"W; WGS 84; elev. 230 m asl). All of . World’s Mammals in Crisis ............................................................................................................................................................ -
The Development of Complex Tooth Shape in Reptiles
ORIGINAL RESEARCH ARTICLE published: 25 February 2014 doi: 10.3389/fphys.2014.00074 The development of complex tooth shape in reptiles Oldrich Zahradnicek 1,MarcelaBuchtova2,3, Hana Dosedelova 2,3 and Abigail S. Tucker 4* 1 Department of Teratology, Institute of Experimental Medicine, v.v.i., Academy of Sciences of the Czech Republic, Prague, Czech Republic 2 Laboratory of Animal Embryology, Institute of Animal Physiology and Genetics, v.v.i., Academy of Sciences of the Czech Republic, Brno, Czech Republic 3 Department of Anatomy, Histology and Embryology, Faculty of Veterinary Medicine, University of Veterinary and Pharmaceutical Sciences, Brno, Czech Republic 4 Department of Craniofacial Development and Stem Cell Biology, and Department of Orthodontics, King’s College London, Guy’s Hospital, London, UK Edited by: Reptiles have a diverse array of tooth shapes, from simple unicuspid to complex Cyril Charles, Ecole Normale multicuspid teeth, reflecting functional adaptation to a variety of diets and eating styles. Supérieure de Lyon, France In addition to cusps, often complex longitudinal labial and lingual enamel crests are Reviewed by: widespread and contribute to the final shape of reptile teeth. The simplest shaped Amel Gritli-Linde, University of Gothenburg, Sweden unicuspid teeth have been found in piscivorous or carnivorous ancestors of recent diapsid Daniel Graf, University of Zurich, reptiles and they are also present in some extant carnivores such as crocodiles and snakes. Switzerland However, the ancestral tooth shape for squamate reptiles is thought to be bicuspid, *Correspondence: indicating an insectivorous diet. The development of bicuspid teeth in lizards has recently Abigail S. Tucker, Department of been published, indicating that the mechanisms used to create cusps and crests are very Craniofacial Development and Stem Cell Biology, and Department of distinct from those that shape cusps in mammals. -
Caribbean Anolis Lizards
Animal Behaviour 85 (2013) 1415e1426 Contents lists available at SciVerse ScienceDirect Animal Behaviour journal homepage: www.elsevier.com/locate/anbehav Convergent evolution in the territorial communication of a classic adaptive radiation: Caribbean Anolis lizards Terry J. Ord a,*, Judy A. Stamps b, Jonathan B. Losos c a Evolution and Ecology Research Centre, and School of Biological, Earth and Environmental Sciences, University of New South Wales, Kensington, NSW, Australia b Department of Evolution and Ecology, University of California at Davis, Davis, CA, U.S.A. c Museum of Comparative Zoology and Department of Organismic and Evolutionary Biology, Harvard University, Cambridge, MA, U.S.A. article info To demonstrate adaptive convergent evolution, it must be shown that shared phenotypes have evolved Article history: independently in different lineages and that a credible selection pressure underlies adaptive evolution. Received 11 December 2012 There are a number of robust examples of adaptive convergence in morphology for which both these Initial acceptance 4 February 2013 criteria have been met, but examples from animal behaviour have rarely been tested as rigorously. Final acceptance 15 March 2013 Adaptive convergence should be common in behaviour, especially behaviour used for communication, Available online 3 May 2013 because the environment often shapes the evolution of signal design. In this study we report on the origins MS. number: A12-00933 of a shared design of a territorial display among Anolis species of lizards from two island radiations in the Caribbean. These lizards perform an elaborate display that consists of a complex series of headbobs and Keywords: dewlap extensions. The way in which these movements are incorporated into displays is generally species adaptation specific, but species on the islands of Jamaica and Puerto Rico also share fundamental aspects in display Anolis lizard design, resulting in two general display types. -
Phylogeography and Population Genetic Structure of the Ornate Dragon Lizard, Ctenophorus Ornatus
Phylogeography and Population Genetic Structure of the Ornate Dragon Lizard, Ctenophorus ornatus Esther Levy*, W. Jason Kennington, Joseph L. Tomkins, Natasha R. LeBas Centre for Evolutionary Biology, School of Animal Biology, The University of Western Australia, Perth, Western Australia Abstract Species inhabiting ancient, geologically stable landscapes that have been impacted by agriculture and urbanisation are expected to have complex patterns of genetic subdivision due to the influence of both historical and contemporary gene flow. Here, we investigate genetic differences among populations of the granite outcrop-dwelling lizard Ctenophorus ornatus, a phenotypically variable species with a wide geographical distribution across the south-west of Western Australia. Phylogenetic analysis of mitochondrial DNA sequence data revealed two distinct evolutionary lineages that have been isolated for more than four million years within the C. ornatus complex. This evolutionary split is associated with a change in dorsal colouration of the lizards from deep brown or black to reddish-pink. In addition, analysis of microsatellite data revealed high levels of genetic structuring within each lineage, as well as strong isolation by distance at multiple spatial scales. Among the 50 outcrop populations’ analysed, non-hierarchical Bayesian clustering analysis revealed the presence of 23 distinct genetic groups, with outcrop populations less than 4 km apart usually forming a single genetic group. When a hierarchical analysis was carried out, almost every outcrop was assigned to a different genetic group. Our results show there are multiple levels of genetic structuring in C. ornatus, reflecting the influence of both historical and contemporary evolutionary processes. They also highlight the need to recognise the presence of two evolutionarily distinct lineages when making conservation management decisions on this species. -
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. -
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. -
Cfreptiles & Amphibians
HTTPS://JOURNALS.KU.EDU/REPTILESANDAMPHIBIANSTABLE OF CONTENTS IRCF REPTILES & AMPHIBIANSREPTILES • VOL15, & N AMPHIBIANSO 4 • DEC 2008 •189 28(1):30–31 • APR 2021 IRCF REPTILES & AMPHIBIANS CONSERVATION AND NATURAL HISTORY TABLE OF CONTENTS CoprophagyFEATURE ARTICLES and Cannibalism in the Cuban . Chasing Bullsnakes (Pituophis catenifer sayi) in Wisconsin: GreenOn the Road Anole,to Understanding the Ecology Anolis and Conservation of theporcatus Midwest’s Giant Serpent ...................... Gray Joshua M. Kapfer1840 190 . The Shared History of Treeboas (Corallus grenadensis) and Humans on Grenada: A Hypothetical Excursion(Squamata: ............................................................................................................................ Dactyloidae)Robert W. Henderson 198 RESEARCH ARTICLES . The Texas Horned Lizard in Central and Western TexasLuis ....................... F. de Armas Emily Henry, Jason Brewer, Krista Mougey, and Gad Perry 204 . The Knight Anole (Anolis equestris) in Florida .............................................P.O. Box 4327, San AntonioBrian J. deCamposano, los Baños, Kenneth Artemisa L. Krysko, Province Kevin 38100,M. Enge, Cuba Ellen M.([email protected]) Donlan, and Michael Granatosky 212 CONSERVATION ALERT . World’s Mammals in Crisis ............................................................................................................................................................. 220 oprophagy in. herbivorousMore Than Mammals reptiles, .............................................................................................................................. -
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. -
Phenotypic Variation and the Behavioral Ecology of Lizards
Phenotypic Variation and the Behavioral Ecology of Lizards The Harvard community has made this article openly available. Please share how this access benefits you. Your story matters Citable link http://nrs.harvard.edu/urn-3:HUL.InstRepos:40046431 Terms of Use This article was downloaded from Harvard University’s DASH repository, and is made available under the terms and conditions applicable to Other Posted Material, as set forth at http:// nrs.harvard.edu/urn-3:HUL.InstRepos:dash.current.terms-of- use#LAA Phenotypic Variation and the Behavioral Ecology of Lizards A dissertation presented by Ambika Kamath to The Department of Organismic and Evolutionary Biology in partial fulfillment of the requirements for the degree of Doctor of Philosophy in the subject of Biology Harvard University Cambridge, Massachusetts March 2017 © 2017 Ambika Kamath All rights reserved. Dissertation Advisor: Professor Jonathan Losos Ambika Kamath Phenotypic Variation and the Behavioral Ecology of Lizards Abstract Behavioral ecology is the study of how animal behavior evolves in the context of ecology, thus melding, by definition, investigations of how social, ecological, and evolutionary forces shape phenotypic variation within and across species. Framed thus, it is apparent that behavioral ecology also aims to cut across temporal scales and levels of biological organization, seeking to explain the long-term evolutionary trajectory of populations and species by understanding short-term interactions at the within-population level. In this dissertation, I make the case that paying attention to individuals’ natural history— where and how individual organisms live and whom and what they interact with, in natural conditions—can open avenues into studying the behavioral ecology of previously understudied organisms, and more importantly, recast our understanding of taxa we think we know well. -
Curly-Tailed Lizard SCIENTIFIC NAME There Are Five Species, Leiocephalus Carinatus, L
Artwork by Dominic Cant Curly-tailed Lizard SCIENTIFIC NAME There are five species, Leiocephalus carinatus, L. greenwayi, L. inaguae, L. loxogrammus and L. punctatus and nine sub-species in the Bahamas. DESCRIPTION The curly tailed lizards are medium sized lizards averaging about 18 cm (7 inches) in total length. In the Bahamas they tend to range from brown to grey and have a range of different markings on them depending upon the species. In some species the females are noticeably smaller than the males and some even display a more conspicuous colouration than their male counterparts, particularly when gravid (egg bearing). The most characteristic feature of these lizards is their tail which curls over their back, similar to that of a scorpion, and lends the lizard its name. DIET Curly tails can be considered omnivores, however insects form a major part of their diet. They have been known to eat flowers such as the Rail road vine (Ipomoea pes-caprae), seeds, small fruits, anole lizards, small crustaceans, spiders, roaches, mosquitoes and large quantities of ants. In captivity some males have exhibited a cannibalistic behaviour. REPRODUCTION Male curly tailed lizards are very territorial and fight off rival males. They also display a range of territorial behaviours like head bobbing, tail curling, strutting and inflation of the sides of the neck. The young males begin to exhibit these courtship behaviours Reptiles of the Bahamas at about one year of age. These behaviours will begin in February and usually ends in October when the lizards become generally less active. The leathery eggs are cream coloured and about 25 mm (1 inch) in length with peak hatching time in mid July. -
Phylogeny, Ecomorphological Evolution, and Historical Biogeography of the Anolis Cristatellus Series
Uerpetological Monographs, 18, 2004, 90-126 © 2004 by The Herpetologists' League, Inc. PHYLOGENY, ECOMORPHOLOGICAL EVOLUTION, AND HISTORICAL BIOGEOGRAPHY OF THE ANOLIS CRISTATELLUS SERIES MATTHEW C. BRANDLEY^''^'"' AND KEVIN DE QUEIROZ^ ^Sam Noble Oklahoma Museum of Natural History and Department of Zoology, The University of Oklahoma, Norman, OK 73072, USA ^Department of Zoology, National Museum of Natural History, Smithsonian Institution, Washington, DC 20,560, USA ABSTRACT: TO determine the evolutionary relationships within the Anolis cristatellus series, we employed phylogenetic analyses of previously published karyotype and allozyme data as well as newly collected morphological data and mitochondrial DNA sequences (fragments of the 12S RNA and cytochrome b genes). The relationships inferred from continuous maximum likelihood reanalyses of allozyme data were largely poorly supported. A similar analysis of the morphological data gave strong to moderate support for sister relationships of the two included distichoid species, the two trunk-crown species, the grass-bush species A. poncensis and A. pulchellus, and a clade of trunk-ground and grass-bush species. The results of maximum likelihood and Bayesian analyses of the 12S, cyt b, and combined mtDNA data sets were largely congruent, but nonetheless exhibit some differences both with one another and with those based on the morphological data. We therefore took advantage of the additive properties of likelihoods to compare alternative phylogenetic trees and determined that the tree inferred from the combined 12S and cyt b data is also the best estimate of the phylogeny for the morphological and mtDNA data sets considered together. We also performed mixed-model Bayesian analyses of the combined morphology and mtDNA data; the resultant tree was topologically identical to the combined mtDNA tree with generally high nodal support.