2011: a Survey of Disease Conditions in Pet Store Reptiles with Diagnostic and Therapy Options
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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. -
UC Berkeley UC Berkeley Electronic Theses and Dissertations
UC Berkeley UC Berkeley Electronic Theses and Dissertations Title Neuromechanics of Maneuverability: Sensory-Neural and Mechanical Processing for the Control of High-Speed Locomotion Permalink https://escholarship.org/uc/item/1b79g7xw Author Mongeau, Jean-Michel Publication Date 2013 Peer reviewed|Thesis/dissertation eScholarship.org Powered by the California Digital Library University of California Neuromechanics of Maneuverability: Sensory-Neural and Mechanical Processing for the Control of High-Speed Locomotion By Jean-Michel Mongeau A dissertation submitted in partial satisfaction of the requirements for the degree of Doctor of Philosophy in Biophysics in the Graduate Division of the University of California, Berkeley Committee in charge: Professor Robert J. Full, Chair Professor Noah J. Cowan Professor Ronald S. Fearing Professor Frederic E. Theunissen Spring 2013 Neuromechanics of Maneuverability: Sensory-Neural and Mechanical Processing for the Control of High-Speed Locomotion 2013 by Jean-Michel Mongeau Abstract Neuromechanics of Maneuverability: Sensory-Neural and Mechanical Processing for the Control of High-Speed Locomotion by Jean-Michel Mongeau Doctor of Philosophy in Biophysics University of California, Berkeley Professor Robert J. Full, Chair Maneuverability in animals is unparalleled when compared to the most maneuverable human- engineered mobile robot. Maneuverability arises in part from animals’ ability to integrate multimodal sensory information with an ongoing motor program while interacting within a spatiotemporally -
COSTA RICA: the Introtour (Group 1) Feb 2017
Tropical Birding Trip Report COSTA RICA: The Introtour (Group 1) Feb 2017 A Tropical Birding set departure tour COSTA RICA: The Introtour 13th - 23rd February 2017 (Group 1) Tour Leader: Sam Woods (Report and all photos by Sam Woods) This Keel-billed Toucan lit up our first afternoon, near Braulio Carrillo National Park. The same day also featured Thicket Antpitta and THREE species of owl during the daytime… Ferruginous Pygmy, Crested and Spectacled Owls. 1 www.tropicalbirding.com +1-409-515-9110 [email protected] Page Tropical Birding Trip Report COSTA RICA: The Introtour (Group 1) Feb 2017 INTRODUCTION There can be few countries in the World as welcoming to birders as Costa Rica; everywhere we went birds were plentiful and frequently people with binoculars were in attendance too. Indeed, Costa Rica makes you feel odd if you are NOT wearing a pair. We enjoyed a fantastic tour of some of the most revered sites in Costa Rican birding; we started out near San Jose in the dry Central Valley, before driving over to the Caribbean side, where foothill birding was done in and around Braulio Carrillo National Park, and held beautiful birds from the outset, like Black-and-yellow Tanager, Black-thighed Grosbeak, and daytime Spectacled and Crested Owls. A tour first was also provided by a Thicket Antpitta seen well by all. From there we continued downslope to the lowlands of that side, and the world famous La Selva Biological Station. La Selva is a place where birds feel particularly plentiful, and we racked up a heady list of birds on our one and a half days there, including Rufous and Broad-billed Motmots, Black-throated Trogon, Pale-billed, Cinnamon and Chestnut-colored Woodpeckers, Keel-billed and Yellow-throated Toucans, and Great Curassow, to name just a few of the highlights, which also included several two-toed sloths, the iconic Red-eyed Tree Frog (photo last page), and Strawberry Poison Dart Frogs of the much publicized “blue jeans” form that adorns so many tourist posters in this Sarapiqui region. -
Evolution of the Iguanine Lizards (Sauria, Iguanidae) As Determined by Osteological and Myological Characters David F
Brigham Young University Science Bulletin, Biological Series Volume 12 | Number 3 Article 1 1-1971 Evolution of the iguanine lizards (Sauria, Iguanidae) as determined by osteological and myological characters David F. Avery Department of Biology, Southern Connecticut State College, New Haven, Connecticut Wilmer W. Tanner Department of Zoology, Brigham Young University, Provo, Utah Follow this and additional works at: https://scholarsarchive.byu.edu/byuscib Part of the Anatomy Commons, Botany Commons, Physiology Commons, and the Zoology Commons Recommended Citation Avery, David F. and Tanner, Wilmer W. (1971) "Evolution of the iguanine lizards (Sauria, Iguanidae) as determined by osteological and myological characters," Brigham Young University Science Bulletin, Biological Series: Vol. 12 : No. 3 , Article 1. Available at: https://scholarsarchive.byu.edu/byuscib/vol12/iss3/1 This Article is brought to you for free and open access by the Western North American Naturalist Publications at BYU ScholarsArchive. It has been accepted for inclusion in Brigham Young University Science Bulletin, Biological Series by an authorized editor of BYU ScholarsArchive. For more information, please contact [email protected], [email protected]. S-^' Brigham Young University f?!AR12j97d Science Bulletin \ EVOLUTION OF THE IGUANINE LIZARDS (SAURIA, IGUANIDAE) AS DETERMINED BY OSTEOLOGICAL AND MYOLOGICAL CHARACTERS by David F. Avery and Wilmer W. Tanner BIOLOGICAL SERIES — VOLUME Xil, NUMBER 3 JANUARY 1971 Brigham Young University Science Bulletin -
Prolonged Poststrike Elevation in Tongue-Flicking Rate with Rapid Onset in Gila Monster, <Emphasis Type="Italic">
Journal of Chemical Ecology, Vol. 20. No. 11, 1994 PROLONGED POSTSTRIKE ELEVATION IN TONGUE- FLICKING RATE WITH RAPID ONSET IN GILA MONSTER, Heloderma suspectum: RELATION TO DIET AND FORAGING AND IMPLICATIONS FOR EVOLUTION OF CHEMOSENSORY SEARCHING WILLIAM E. COOPER, JR. I'* CHRISTOPHER S. DEPERNO I and JOHNNY ARNETT 2 ~Department of Biology Indiana University-Purdue University Fort Wayne Fort Wayne. bldiana 46805 2Department of Herpetology Cincinnati Zoo and Botanical Garden Cincinnati, Ohio 45220 (Received May 6, 1994; accepted June 27, 1994) Abstract--Experimental tests showed that poststrike elevation in tongue-flick- ing rate (PETF) and strike-induced chemosensory searching (SICS) in the gila monster last longer than reported for any other lizard. Based on analysis of numbers of tongue-flicks emitted in 5-rain intervals, significant PETF was detected in all intervals up to and including minutes 41~-5. Using 10-rain intervals, PETF lasted though minutes 46-55. Two of eight individuals con- tinued tongue-flicking throughout the 60 rain after biting prey, whereas all individuals ceased tongue-flicking in a control condition after minute 35. The apparent presence of PETF lasting at least an hour in some individuals sug- gests that there may be important individual differences in duration of PETF. PETF and/or SICS are present in all families of autarchoglossan lizards stud- ied except Cordylidae, the only family lacking lingually mediated prey chem- ical discrimination. However, its duration is known to be greater than 2-rain only in Helodermatidae and Varanidae, the living representatives of Vara- noidea_ That prolonged PETF and S1CS are typical of snakes provides another character supporting a possible a varanoid ancestry for Serpentes. -
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. -
Evolution of Limblessness
Evolution of Limblessness Evolution of Limblessness Early on in life, many people learn that lizards have four limbs whereas snakes have none. This dichotomy not only is inaccurate but also hides an exciting story of repeated evolution that is only now beginning to be understood. In fact, snakes represent only one of many natural evolutionary experiments in lizard limblessness. A similar story is also played out, though to a much smaller extent, in amphibians. The repeated evolution of snakelike tetrapods is one of the most striking examples of parallel evolution in animals. This entry discusses the evolution of limblessness in both reptiles and amphibians, with an emphasis on the living reptiles. Reptiles Based on current evidence (Wiens, Brandley, and Reeder 2006), an elongate, limb-reduced, snakelike morphology has evolved at least twenty-five times in squamates (the group containing lizards and snakes), with snakes representing only one such origin. These origins are scattered across the evolutionary tree of squamates, but they seem especially frequent in certain families. In particular, the skinks (Scincidae) contain at least half of all known origins of snakelike squamates. But many more origins within the skink family will likely be revealed as the branches of their evolutionary tree are fully resolved, given that many genera contain a range of body forms (from fully limbed to limbless) and may include multiple origins of snakelike morphology as yet unknown. These multiple origins of snakelike morphology are superficially similar in having reduced limbs and an elongate body form, but many are surprisingly different in their ecology and morphology. This multitude of snakelike lineages can be divided into two ecomorphs (a are surprisingly different in their ecology and morphology. -
Lizard ID Guide
Lizards of Anderson County, TN Lizards are extraordinary gifts of nature. World-wide there are close to 6,000 species. The United States is home to more than100 native species, along with many exotic species that have become established, especially in Florida. Tennessee has 9 species, 6 of which are listed for Anderson County. Some are fairly widespread and easy to observe, such as the Common Five-lined Skink below. Unfortunately, the liberal use of pesticides, combined with predation by free roaming house cats have taken a heavy toll on our lizard populations. Most lizards are insect eating machines and their ecological services should be promoted through backyard and schoolyard wildlife habitat projects. Lizard watching is great fun, and over time, observers can gain interesting insights into lizard behavior. Your backyard may be a good place to start your lizarding career. This guide will be helpful for identifying our local lizards and will also provide you with examples of lizard behaviors to observe. Some species must be captured—this can be challenging—to insure accurate identification. Please see the back page for more resources. Lizarding Lizard watching, often referred to as lizarding, will likely never be as popular as bird watching (birding), but there is an advantage to being a “lizarder.” Unlike birders, you don’t need to be an early riser. Bright sunny days with warm temperatures are the keys for successful lizarding, but like birding, close-up binoculars are helpful. A lizard’s life centers around three performance activities: 1) avoiding predators, 2) feeding, and 3) reproduction. Lizard performance is all about optimal body temperature. -
Molecular Phylogenetics and Evolution 55 (2010) 153–167
Molecular Phylogenetics and Evolution 55 (2010) 153–167 Contents lists available at ScienceDirect Molecular Phylogenetics and Evolution journal homepage: www.elsevier.com/locate/ympev Conservation phylogenetics of helodermatid lizards using multiple molecular markers and a supertree approach Michael E. Douglas a,*, Marlis R. Douglas a, Gordon W. Schuett b, Daniel D. Beck c, Brian K. Sullivan d a Illinois Natural History Survey, Institute for Natural Resource Sustainability, University of Illinois, Champaign, IL 61820, USA b Department of Biology and Center for Behavioral Neuroscience, Georgia State University, Atlanta, GA 30303-3088, USA c Department of Biological Sciences, Central Washington University, Ellensburg, WA 98926, USA d Division of Mathematics & Natural Sciences, Arizona State University, Phoenix, AZ 85069, USA article info abstract Article history: We analyzed both mitochondrial (MT-) and nuclear (N) DNAs in a conservation phylogenetic framework to Received 30 June 2009 examine deep and shallow histories of the Beaded Lizard (Heloderma horridum) and Gila Monster (H. Revised 6 December 2009 suspectum) throughout their geographic ranges in North and Central America. Both MTDNA and intron Accepted 7 December 2009 markers clearly partitioned each species. One intron and MTDNA further subdivided H. horridum into its Available online 16 December 2009 four recognized subspecies (H. n. alvarezi, charlesbogerti, exasperatum, and horridum). However, the two subspecies of H. suspectum (H. s. suspectum and H. s. cinctum) were undefined. A supertree approach sus- Keywords: tained these relationships. Overall, the Helodermatidae is reaffirmed as an ancient and conserved group. Anguimorpha Its most recent common ancestor (MRCA) was Lower Eocene [35.4 million years ago (mya)], with a 25 ATPase Enolase my period of stasis before the MRCA of H. -
Evolution of the Iguanine Lizards (Sauria, Iguanidae) As Determined by Osteological and Myological Characters
Brigham Young University BYU ScholarsArchive Theses and Dissertations 1970-08-01 Evolution of the iguanine lizards (Sauria, Iguanidae) as determined by osteological and myological characters David F. Avery Brigham Young University - Provo Follow this and additional works at: https://scholarsarchive.byu.edu/etd Part of the Life Sciences Commons BYU ScholarsArchive Citation Avery, David F., "Evolution of the iguanine lizards (Sauria, Iguanidae) as determined by osteological and myological characters" (1970). Theses and Dissertations. 7618. https://scholarsarchive.byu.edu/etd/7618 This Dissertation is brought to you for free and open access by BYU ScholarsArchive. It has been accepted for inclusion in Theses and Dissertations by an authorized administrator of BYU ScholarsArchive. For more information, please contact [email protected], [email protected]. EVOLUTIONOF THE IGUA.NINELI'ZiUIDS (SAUR:U1., IGUANIDAE) .s.S DETEH.MTNEDBY OSTEOLOGICJJJAND MYOLOGIC.ALCHARA.C'l'Efi..S A Dissertation Presented to the Department of Zoology Brigham Yeung Uni ver·si ty Jn Pa.rtial Fillf.LLlment of the Eequ:Lr-ements fer the Dz~gree Doctor of Philosophy by David F. Avery August 197U This dissertation, by David F. Avery, is accepted in its present form by the Department of Zoology of Brigham Young University as satisfying the dissertation requirement for the degree of Doctor of Philosophy. 30 l'/_70 ()k ate Typed by Kathleen R. Steed A CKNOWLEDGEHENTS I wish to extend my deepest gratitude to the members of m:r advisory committee, Dr. Wilmer W. Tanner> Dr. Harold J. Bissell, I)r. Glen Moore, and Dr. Joseph R. Murphy, for the, advice and guidance they gave during the course cf this study. -
Muscle Biochemistry and Body Shape Explain Ontogenetic Variation of Anti
© 2016. Published by The Company of Biologists Ltd | Journal of Experimental Biology (2016) 219, 1649-1658 doi:10.1242/jeb.130740 RESEARCH ARTICLE Beyond body size: muscle biochemistry and body shape explain ontogenetic variation of anti-predatory behaviour in the lizard Salvator merianae Fábio Cury de Barros1, JoséEduardo de Carvalho2, Augusto Shinya Abe3 and Tiana Kohlsdorf1,* ABSTRACT When facing a predator and after choosing among possible anti- Anti-predatory behaviour evolves under the strong action of natural predatory strategies, animals are likely to adjust the characteristics selection because the success of individuals avoiding predation and intensity of the elected behavioural response according to the essentially defines their fitness. Choice of anti-predatory strategies is perceived level of predation risk (Brown et al., 2006; Greene, 1988; defined by prey characteristics as well as environmental temperature. Martín and López, 2003; Ydenberg and Dill, 1986). Many factors An additional dimension often relegated in this multilevel equation is might influence the choice and intensity of the elected anti- the ontogenetic component. In the tegu Salvator merianae, adults run predatory tactic, such as local conditions [i.e. environmental away from predators at high temperatures but prefer fighting when it is temperature, amount of light/period of day and vegetation cover/ cold, whereas juveniles exhibit the same flight strategy within a wide terrain characteristics (Savino and Stein, 1989; Christensen and thermal range. Here, we integrate physiology and morphology to Persson, 1993; Brodie and Russell, 1999; Shine et al., 2000, 2003; understand ontogenetic variation in the temperature-dependent shift Schulte et al., 2004; Durso and Mullin, 2014)] or type and density of of anti-predatory behaviour in these lizards. -
Class: Amphibia Amphibians Order
CLASS: AMPHIBIA AMPHIBIANS ANNIELLIDAE (Legless Lizards & Allies) CLASS: AMPHIBIA AMPHIBIANS Anniella (Legless Lizards) ORDER: ANURA FROGS AND TOADS ___Silvery Legless Lizard .......................... DS,RI,UR – uD ORDER: ANURA FROGS AND TOADS BUFONIDAE (True Toad Family) BUFONIDAE (True Toad Family) ___Southern Alligator Lizard ............................ RI,DE – fD Bufo (True Toads) Suborder: SERPENTES SNAKES Bufo (True Toads) ___California (Western) Toad.............. AQ,DS,RI,UR – cN ___California (Western) Toad ............. AQ,DS,RI,UR – cN ANNIELLIDAE (Legless Lizards & Allies) Anniella ___Red-spotted Toad ...................................... AQ,DS - cN BOIDAE (Boas & Pythons) ___Red-spotted Toad ...................................... AQ,DS - cN (Legless Lizards) Charina (Rosy & Rubber Boas) ___Silvery Legless Lizard .......................... DS,RI,UR – uD HYLIDAE (Chorus Frog and Treefrog Family) ___Rosy Boa ............................................ DS,CH,RO – fN HYLIDAE (Chorus Frog and Treefrog Family) Pseudacris (Chorus Frogs) Pseudacris (Chorus Frogs) Suborder: SERPENTES SNAKES ___California Chorus Frog ............ AQ,DS,RI,DE,RO – cN COLUBRIDAE (Colubrid Snakes) ___California Chorus Frog ............ AQ,DS,RI,DE,RO – cN ___Pacific Chorus Frog ....................... AQ,DS,RI,DE – cN Arizona (Glossy Snakes) ___Pacific Chorus Frog ........................AQ,DS,RI,DE – cN BOIDAE (Boas & Pythons) ___Glossy Snake ........................................... DS,SA – cN Charina (Rosy & Rubber Boas) RANIDAE (True Frog Family)