Peters's Rock Agama in Florida1
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Herpetological Journal SHORT NOTE
Volume 28 (April 2018), 93-95 SHORT NOTE Herpetological Journal Published by the British Intersexuality in Helicops infrataeniatus Jan, 1865 Herpetological Society (Dipsadidae: Hydropsini) Ruth A. Regnet1, Fernando M. Quintela1, Wolfgang Böhme2 & Daniel Loebmann1 1Universidade Federal do Rio Grande, Instituto de Ciências Biológicas, Laboratório de Vertebrados. Av. Itália km 8, CEP: 96203-900, Vila Carreiros, Rio Grande, Rio Grande do Sul, Brazil 2Zoologisches Forschungsmuseum A. Koenig, Adenauerallee 160, D-53113 Bonn, Germany Herein, we describe the first case of intersexuality in the are viviparous, and interestingly, H. angulatus exhibits Hydropsini tribe. After examination of 720 specimens both reproductive modes (Rossman, 1984; Aguiar & Di- of Helicops infrataeniatus Jan, 1865, we discovered Bernardo, 2005; Braz et al., 2016). Helicops infrataeniatus one individual that presented feminine and masculine has a wide distribution that encompasses south- reproductive features. The specimen was 619 mm long, southeastern Brazil, southern Paraguay, North-eastern with seven follicles in secondary stage, of different shapes Argentina and Uruguay (Deiques & Cechin, 1991; Giraudo, and sizes, and a hemipenis with 13.32 and 13.57 mm in 2001; Carreira & Maneyro, 2013). At the coastal zone of length. The general shape of this organ is similar to that southernmost Brazil, H. infrataeniatus is among the most observed in males, although it is smaller and does not abundant species in many types of limnic and estuarine present conspicuous spines along its body. Deformities environments (Quintela & Loebmann, 2009; Regnet found in feminine and masculine structures suggest that et al., 2017). In October 2015 at the Laranjal beach, this specimen might not be reproductively functional. municipality of Pelotas, state of Rio Grande do Sul, Brazil (31°46’S, 52°13’W), a remarkable aggregation of reptiles Key words: Follicles, hemipenis, hermaphroditism, water and caecilians occurred after a flood event associated to snake. -
Movement and Habitat Use by Adult and Juvenile Toad-Headed Agama Lizards (Phrynocephalus Versicolor Strauch, 1876) in the Eastern Gobi Desert, Mongolia
Herpetology Notes, volume 12: 717-719 (2019) (published online on 07 July 2019) Movement and habitat use by adult and juvenile Toad-headed Agama lizards (Phrynocephalus versicolor Strauch, 1876) in the eastern Gobi Desert, Mongolia Douglas Eifler1,* and Maria Eifler1,2 Introduction From 0700–1900 h we walked slowly throughout the study area in search of Toad-headed Agama lizards Phrynocephalus versicolor Strauch, 1876 is a (Phrynocephalus versicolor). When a lizard was small lizard (Agamidae) found in desert and semi- sighted, we captured the animal by hand or noose. desert regions of China, Mongolia, Kazakhstan and We then measured the lizard (snout-to-vent length Kyrgyzstan (Zhao, 1999). The species inhabits areas of (SVL; mm) and mass (g) and sexed adults by probing. sparse vegetation and can be relatively common, with Juveniles were too small to sex. Using non-toxic paint reported densities of up to 400 per hectare (Zhao, 1999). pens, we marked each lizard with a unique colour code In spite of its wide distribution and local abundance, for later identification and to avoid recapture or repeat relatively little detailed ecological information is observations. available, particularly in the northern areas of its range. All focal observations occurred on one day (26 We report our ecological observations on a population August). When an animal was sighted, we positioned of P. versicolor in the Gobi Desert of Mongolia with ourselves 3–5 m from the lizard, waited 5 min for regard to their movement and habitat use. the lizard to acclimate to our presence, and then we began a 10-min observation period. -
The Global Distribution of Tetrapods Reveals a Need for Targeted Reptile
1 The global distribution of tetrapods reveals a need for targeted reptile 2 conservation 3 4 Uri Roll#1,2, Anat Feldman#3, Maria Novosolov#3, Allen Allison4, Aaron M. Bauer5, Rodolphe 5 Bernard6, Monika Böhm7, Fernando Castro-Herrera8, Laurent Chirio9, Ben Collen10, Guarino R. 6 Colli11, Lital Dabool12 Indraneil Das13, Tiffany M. Doan14, Lee L. Grismer15, Marinus 7 Hoogmoed16, Yuval Itescu3, Fred Kraus17, Matthew LeBreton18, Amir Lewin3, Marcio Martins19, 8 Erez Maza3, Danny Meirte20, Zoltán T. Nagy21, Cristiano de C. Nogueira19, Olivier S.G. 9 Pauwels22, Daniel Pincheira-Donoso23, Gary Powney24, Roberto Sindaco25, Oliver Tallowin3, 10 Omar Torres-Carvajal26, Jean-François Trape27, Enav Vidan3, Peter Uetz28, Philipp Wagner5,29, 11 Yuezhao Wang30, C David L Orme6, Richard Grenyer✝1 and Shai Meiri✝*3 12 13 # Contributed equally to the paper 14 ✝ Contributed equally to the paper 15 * Corresponding author 16 17 Affiliations: 18 1 School of Geography and the Environment, University of Oxford, Oxford, OX13QY, UK. 19 2 Mitrani Department of Desert Ecology, The Jacob Blaustein Institutes for Desert Research, 20 Ben-Gurion University, Midreshet Ben-Gurion 8499000, Israel. (Current address) 21 3 Department of Zoology, Tel-Aviv University, Tel-Aviv 6997801, Israel. 22 4 Hawaii Biological Survey, 4 Bishop Museum, Honolulu, HI 96817, USA. 23 5 Department of Biology, Villanova University, Villanova, PA 19085, USA. 24 6 Department of Life Sciences, Imperial College London, Silwood Park Campus Silwood Park, 25 Ascot, Berkshire, SL5 7PY, UK 26 7 Institute of Zoology, Zoological Society of London, London NW1 4RY, UK. 27 8 School of Basic Sciences, Physiology Sciences Department, Universidad del Valle, Colombia. -
An Inventory of Online Reptile Images
Zootaxa 0000 (0): 000–000 ISSN 1175-5326 (print edition) https://www.mapress.com/j/zt/ Article ZOOTAXA Copyright © 2020 Magnolia Press ISSN 1175-5334 (online edition) https://doi.org/10.11646/zootaxa.0000.0.0 http://zoobank.org/urn:lsid:zoobank.org:pub:00000000-0000-0000-0000-00000000000 An inventory of online reptile images BENJAMIN MICHAEL MARSHALL1*, PAUL FREED2, LAURIE J. VITT3, PEDRO BERNARDO4, GERNOT VOGEL5, SEBASTIAN LOTZKAT6, MICHAEL FRANZEN7, JAKOB HALLERMANN8, RICHARD D. SAGE9, BRIAN BUSH10, MARCELO RIBEIRO DUARTE11, LUCIANO JAVIER AVILA12, DAVID JANDZIK13, BORIS KLUSMEYER14, BRAD MARYAN15, JIŘÍ HOŠEK16, PETER UETZ17* 1Suranaree University of Technology, Nakhon Ratchasima, Thailand �[email protected]; https://orcid.org/0000-0001-9554-0605 2Scotts Mills, Oregon 97375, USA. �[email protected] 3Sam Noble Museum, Norman, Oklahoma 73072, USA. �[email protected] 4Royal Ontario Museum, Toronto, ON, Canada. �[email protected] 5Society for Southeast Asian Herpetology, Heidelberg, Germany �[email protected]; https://orcid.org/0000-0002-4542-518X 6Staatliches Museum für Naturkunde Stuttgart, Stuttgart, Germany �[email protected]; https://orcid.org/0000-0001-8171-9321 7Zoologische Staatssammlung München (ZSM-SNSB), 81247 München, Germany. �[email protected] 8Universität Hamburg, Centrum für Naturkunde, Hamburg, Germany �[email protected]; https://orcid.org/0000-0002-8835-9303 9Museum of Vertebrate Zoology, University of California, Berkeley, California 94720, and Sociedad Naturalista Andino Patagónica (SNAP), S. C. de Bariloche, Río Negro, 8400, Argentina. �[email protected]; https://orcid.org/0000-0002-0897-6927 10Stoneville, WA, Australia. �[email protected]; https://orcid.org/0000-0002-3487-6620 11Instituto Butantan, Laboratório de Coleções Zoológicas, São Paulo, Brazil. -
Summary Report of Freshwater Nonindigenous Aquatic Species in U.S
Summary Report of Freshwater Nonindigenous Aquatic Species in U.S. Fish and Wildlife Service Region 4—An Update April 2013 Prepared by: Pam L. Fuller, Amy J. Benson, and Matthew J. Cannister U.S. Geological Survey Southeast Ecological Science Center Gainesville, Florida Prepared for: U.S. Fish and Wildlife Service Southeast Region Atlanta, Georgia Cover Photos: Silver Carp, Hypophthalmichthys molitrix – Auburn University Giant Applesnail, Pomacea maculata – David Knott Straightedge Crayfish, Procambarus hayi – U.S. Forest Service i Table of Contents Table of Contents ...................................................................................................................................... ii List of Figures ............................................................................................................................................ v List of Tables ............................................................................................................................................ vi INTRODUCTION ............................................................................................................................................. 1 Overview of Region 4 Introductions Since 2000 ....................................................................................... 1 Format of Species Accounts ...................................................................................................................... 2 Explanation of Maps ................................................................................................................................ -
Reptile Rap Newsletter of the South Asian Reptile Network ISSN 2230-7079 No.15 | January 2013 Date of Publication: 22 January 2013 1
Reptile Rap Newsletter of the South Asian Reptile Network No.15 | January 2013 ISSN 2230-7079 Date of publication: 22 January 2013 1. Crocodile, 1. 2. Crocodile, Caiman, 3. Gharial, 4.Common Chameleon, 5. Chameleon, 9. Chameleon, Flap-necked 8. Chameleon Flying 7. Gecko, Dragon, Ptychozoon Chamaeleo sp. Fischer’s 10 dilepsis, 6. &11. Jackson’s Frill-necked 21. Stump-tailed Skink, 20. Gila Monster, Lizard, Green Iguana, 19. European Iguana, 18. Rhinoceros Antillean Basilisk, Iguana, 17. Lesser 16. Green 15. Common Lizard, 14. Horned Devil, Thorny 13. 12. Uromastyx, Lizard, 34. Eastern Tortoise, 33. 32. Rattlesnake Indian Star cerastes, 22. 31. Boa,Cerastes 23. Python, 25. 24. 30. viper, Ahaetulla Grass Rhinoceros nasuta Snake, 29. 26. 27. Asp, Indian Naja Snake, 28. Cobra, haje, Grater African 46. Ceratophrys, Bombina,45. 44. Toad, 43. Bullfrog, 42. Frog, Common 41. Turtle, Sea Loggerhead 40. Trionychidae, 39. mata Mata 38. Turtle, Snake-necked Argentine 37. Emydidae, 36. Tortoise, Galapagos 35. Turtle, Box 48. Marbled Newt Newt, Crested 47. Great Salamander, Fire Reptiles, illustration by Adolphe Millot. Source: Nouveau Larousse Illustré, edited by Claude Augé, published in Paris by Librarie Larousse 1897-1904, this illustration from vol. 7 p. 263 7 p. vol. from 1897-1904, this illustration Larousse Librarie by published in Paris Augé, Claude by edited Illustré, Larousse Nouveau Source: Millot. Adolphe by illustration Reptiles, www.zoosprint.org/Newsletters/ReptileRap.htm OPEN ACCESS | FREE DOWNLOAD REPTILE RAP #15, January 2013 Contents A new record of the Cochin Forest Cane Turtle Vijayachelys silvatica (Henderson, 1912) from Shendurney Wildlife Sanctuary, Kerala, India Arun Kanagavel, 3–6pp New Record of Elliot’s Shieldtail (Gray, 1858) in Seshachalam Biosphere Reserve, Eastern Ghats, Andhra Pradesh, India M. -
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. -
Diversity and Conservation of Amphibians and Reptiles in North Punjab, Pakistan
Diversity and conservation of amphibians and reptiles in North Punjab, Pakistan. MUHAMMAD RAIS, SARA BALOCH, JAVERIA REHMAN, MAQSOOD ANWAR, IFTIKHAR HUSSAIN AND TARIQ MAHMOOD Department of Wildlife Management, PMAS Arid Agriculture University Rawalpindi, Pakistan. Corresponding Author: Muhammad Rais, Visiting Scholar, Department of Biology, Indiana-Purdue University Fort Wayne, Indiana, USA. Email: [email protected] ABSTRACT - Amphibians and reptiles are the most neglected and least studied wildlife groups in Pakistan. The present study was conducted in the selected areas of districts Rawalpindi, Islamabad and Chakwal, North Punjab, Pakistan, to obtain data on herpetofaunal species richness and abundance from February, 2010 to January, 2011 using area-constrained searches. A total of 35 species of amphibians and reptiles (29 genera, 16 families, four orders) were recorded from the study area. Of the recorded species, 30 were reptiles (25 genera, 13 families, three orders) and five were amphibians (four genera, three families and a single order). A total of 388 individuals belonging to 11 recognizable taxonomic units (RTUs) with a population density of 0.22 individuals/ ha. and 4.10 encounters were recorded. Of the recorded RTUs, two (lacertids and skinks) were rated as uncommon, seven (hard-shell turtles, soft-shell turtles, agamids, gekkonids, medium and large-sized lizards, non-venomous snakes and venomous snakes) as frequent and two (toads and frogs) as common. Districts Rawalpindi/ Islamabad had higher species richness while District Chakwal had relatively higher species diversity and evenness. Threatened species of the area included the Narrow-headed Soft-shell Turtle (Chitra indica), Indian Soft-shell Turtle (Nilssonia gangetica), Peacock Soft-shell Turtle (Aspideretes hurum), and Brown River Turtle (Pangshura smithii). -
Introduced Amphibians and Reptiles in the Cuban Archipelago
Herpetological Conservation and Biology 10(3):985–1012. Submitted: 3 December 2014; Accepted: 14 October 2015; Published: 16 December 2015. INTRODUCED AMPHIBIANS AND REPTILES IN THE CUBAN ARCHIPELAGO 1,5 2 3 RAFAEL BORROTO-PÁEZ , ROBERTO ALONSO BOSCH , BORIS A. FABRES , AND OSMANY 4 ALVAREZ GARCÍA 1Sociedad Cubana de Zoología, Carretera de Varona km 3.5, Boyeros, La Habana, Cuba 2Museo de Historia Natural ”Felipe Poey.” Facultad de Biología, Universidad de La Habana, La Habana, Cuba 3Environmental Protection in the Caribbean (EPIC), Green Cove Springs, Florida, USA 4Centro de Investigaciones de Mejoramiento Animal de la Ganadería Tropical, MINAGRI, Cotorro, La Habana, Cuba 5Corresponding author, email: [email protected] Abstract.—The number of introductions and resulting established populations of amphibians and reptiles in Caribbean islands is alarming. Through an extensive review of information on Cuban herpetofauna, including protected area management plans, we present the first comprehensive inventory of introduced amphibians and reptiles in the Cuban archipelago. We classify species as Invasive, Established Non-invasive, Not Established, and Transported. We document the arrival of 26 species, five amphibians and 21 reptiles, in more than 35 different introduction events. Of the 26 species, we identify 11 species (42.3%), one amphibian and 10 reptiles, as established, with nine of them being invasive: Lithobates catesbeianus, Caiman crocodilus, Hemidactylus mabouia, H. angulatus, H. frenatus, Gonatodes albogularis, Sphaerodactylus argus, Gymnophthalmus underwoodi, and Indotyphlops braminus. We present the introduced range of each of the 26 species in the Cuban archipelago as well as the other Caribbean islands and document historical records, the population sources, dispersal pathways, introduction events, current status of distribution, and impacts. -
The Mechanism of Tongue Projection in Chameleons Ii
J. exp. Biol. 168, 23-40 (1992) 23 Printed in Great Britain © The Company of Biologists Limited 1992 THE MECHANISM OF TONGUE PROJECTION IN CHAMELEONS II. ROLE OF SHAPE CHANGE IN A MUSCULAR HYDROSTAT BY PETER C. WAINWRIGHT* AND ALBERT F. BENNETT Department of Ecology and Evolutionary Biology, University of California, Irvine, CA 92717, USA Accepted 23 March 1992 Summary In this paper we investigate the interaction between the accelerator muscle (the muscle that powers tongue projection) and the entoglossal process (the tongue's skeletal support) that occurs during tongue projection in chamaeleonid lizards. Previous work has shown that there is a delay of about 185 ms between the onset of accelerator muscle activity and the onset of tongue projection. In conjunction with anatomical observations, in vitro preparations of the accelerator muscle mounted on isolated entoglossal and surrogate processes were stimulated tetanically, and the resulting movements were recorded on video at 200 fields s"1. Three results indicate that morphological features of the entoglossus and the accelerator muscle delay the onset of tongue projection following the onset of accelerator contrac- tion: (I) the entoglossus is parallel-sided along the posterior 90% of its shaft, only tapering at the very tip, (2) the sphincter-like portion of the accelerator muscle, which effects tongue projection, makes up the posterior 63% of the muscle and does not contact the tapered region of the entoglossus at rest, and (3) accelerator muscles mounted on the entoglossus undergo longitudinal extension and lateral constriction for 83 ms following the onset of electrical stimulation, before projecting off the entoglossus. -
Two Species of Malarial Parasite in a West African Lizard
Oecologia (1994) 97:326-332 Springer-Verlag 1994 ORIGINAL PAPER ? Joseph J. Schall Carl R. Bromwich Interspecific interactions tested: two species of malarial parasite in a West African lizard Received: 25 June 1993 / Accepted: 14 December 1993 Abstract Plasmodium giganteum and P. agamae, para- affecting communities of free-living species (competition sites of the rainbow lizard, Agama agama, in West Africa for resources, interference, mutualism, historical chance were studied to determine the nature of any interspecific events), but must also include the influence of the host's interactions between the two malaria species. The plas- immune system which is unique to parasites. The litera- modia are distributed in A. agama throughout the mesic ture on community ecology of free-living organisms has zone of Africa; P. agamae is sometimes found as a soli- long included debate on the relative importance of spe- tary malaria species in populations of the lizard, but P. cies interactions (especially competition) and random giganteum has not been found alone. In 3170 lizards events. This discussion is mirrored in the parasitological from Sierra Leone the prevalence of lizard malaria at 22 literature. Some workers hold that parasite communi- sites varied considerably (8-90% of lizards were infect- ties are structured primarily by competition and there ed), but the ratio of the two species was similar among are "assembly rules" governing coexisting parasite spe- sites (52-91% P. agamae). Larger lizards were more of- cies (Holmes 1961; Esch et al. 1990), whereas others ten infected. Mixed infections occurred 2-5 times more present evidence that these communities are noninterac- often than expected by chance. -
Observations of Infanticide and Cannibalism in Four Species of Cordylid Lizard (Squamata: Cordylidae) in Captivity and the Wild
Herpetology Notes, volume 14: 725-729 (2021) (published online on 21 April 2021) Observations of infanticide and cannibalism in four species of cordylid lizard (Squamata: Cordylidae) in captivity and the wild Daniel van Blerk1,†, Jens Reissig2,†, Julia L. Riley 3,†, John Measey1,*, and James Baxter-Gilbert1 Cannibalism, the consumption of conspecifics, of Africa (Reissig, 2014), from Ethiopia to South Africa is taxonomically widespread and occurs across a (latitudinally) and Angola to Ethiopia (longitudinally). diversity of reptilian species (Polis and Myers, 1985). Here, we present observations of cannibalism by four A long-standing, yet antiquated, perspective views species of cordylid lizard, two from free-living wild cannibalism as an aberrant behaviour (as discussed populations and another two from captive settings. Since in Fox, 1975), but contemporary investigations have the natural history of many cordylid species remains noted its important role in the ecology and evolution of deficient, and several species have been observed to many wild populations (Robbins et al., 2013; Cooper display reasonably high degrees of sociality, like group- et al., 2015; Van Kleek et al., 2018). Examples of this living in Armadillo Lizards, Ouroborus cataphractus include habitat partitioning and optimising resource (Boie, 1828) (Mouton, 2011) and Sungazers, Smaug availability, as seen in juvenile Komodo Dragons, giganteus (Smith, 1844) (Parusnath, 2020), these Varanus komodoensis Ouwens, 1912, taking to the trees observations provide important insights