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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. -
(Testudines: Geoemydidae) from the Azov Sea Coast in the Crimea
Official journal website: Amphibian & Reptile Conservation amphibian-reptile-conservation.org 10(2) [General Section]: 27–29 (e129). Short Communication A record of the Balkan Stripe-necked Terrapin, Mauremys rivulata (Testudines: Geoemydidae) from the Azov Sea Coast in the Crimea 1Oleg V. Kukushkin and 2Daniel Jablonski 1Department of Herpetology, Zoological Institute of Russian Academy of Sciences, Universitetskaya Emb. 1, 199034 Saint Pe- tersburg, RUSSIA 2Department of Zoology, Comenius University in Bratislava, Mlynská dolina, Ilkovičova 6, 842 15 Bratislava, SLOVAKIA Keywords. Mauremys rivulata, first record, Crimea, Kerch peninsula, Azov Sea, overseas dispersal, occasional relocation Citation: Kukushkin O V, Jablonski D. 2016. A record of the Balkan Stripe-necked Terrapin, Mauremys rivulata (Testudines: Geomydidae) from the Azov Sea Coast in Crimea. Amphibian & Reptile Conservation 10(2) [General Section]: 27–29 (e129). Copyright: © 2016 Kukushkin and Jablonski. This is an open-access article distributed under the terms of the Creative Commons Attribution- NonCommercialNoDerivatives 4.0 International License, which permits unrestricted use for non-commercial and education purposes only, in any medium, provided the original author and the official and authorized publication sources are recognized and properly credited. The official and authorized publication credit sources, which will be duly enforced, are as follows: official journal titleAmphibian & Reptile Conservation; official journal website <amphibian-reptile-conservation.org>. Received: 03 September 2016; Accepted: 7 November 2016; Published: 30 November 2016 The Crimean herpetofauna comprises such true Eastern- limestone rocks on the abrasion-accumulative sea coast Mediterranean species as Mediodactylus kotschyi and below the lake (Fig. 1B). In general, the locality remains Zamenis situla (Sillero et al. 2014). The occurrence of typical of habitats of M. -
Accessory Scutes and Asymmetries in European Pond Turtle, Emys
International Journal of Fauna and Biological Studies 2016; 3(3): 127-132 ISSN 2347-2677 IJFBS 2016; 3(3): 127-132 Accessory scutes and asymmetries in European pond Received: 20-03-2016 Accepted: 21-04-2016 turtle, Emys orbicularis (Linnaeus, 1758) and Balkan Enerit Saçdanaku terrapin, Mauremys rivulata (Valenciennes, 1833) from Research Center of Flora and Vlora Bay, western Albania Fauna, Faculty of Natural Sciences, University of Tirana, Albania Enerit Saçdanaku, Idriz Haxhiu Idriz Haxhiu Herpetological Albanian Society Abstract (HAS), Tirana, Albania This study aims to provide the first information about scute anomalies occurring in the population of Emys orbicularis and Mauremys rivulata in the understudied area of Vlora Bay, Albania. Two main different habitats, freshwater channels and ponds were monitored from March 2013 to October 2015. A total of 143 individuals of E. orbicularis and 46 individuals of M. rivulata were captured and checked for the presence of scute anomalies. We found that 3.5% of the captured individuals of E. orbicularis and 13.0% of M. rivulata had conspicuous carapacial scute anomalies. The most common anomaly in both populations of E. orbicularis and M. rivulata was the accessory scutes (between vertebrals, between one costal and one vertebral, etc.) present in 36.3% of individuals. It was observed that 80% of anomalous individuals of E. orbicularis had more than one scute anomaly, while all anomalous individuals of M. rivuata had only one anomaly. Different hypotheses are discussed to explain this findings. Keywords: anomaly, accessory scutes, Emys orbicularis, Mauremys rivulata, population Introduction European pond turtle Emys orbicularis (L., 1758) of the family Emydidae and Balkan Terrapin Mauremys rivulata (Valenciennes, 1883) from the family Geoemydidae are two of the hard- shelled freshwater turtles inhabiting in Albania. -
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 ................................................................................................................................ -
Significant New Records of Amphibians and Reptiles from Georgia, USA
GEOGRAPHIC DISTRIBUTION 597 Herpetological Review, 2015, 46(4), 597–601. © 2015 by Society for the Study of Amphibians and Reptiles Significant New Records of Amphibians and Reptiles from Georgia, USA Distributional maps found in Amphibians and Reptiles of records for a variety of amphibian and reptile species in Georgia. Georgia (Jensen et al. 2008), along with subsequent geographical All records below were verified by David Bechler (VSU), Nikole distribution notes published in Herpetological Review, serve Castleberry (GMNH), David Laurencio (AUM), Lance McBrayer as essential references for county-level occurrence data for (GSU), and David Steen (SRSU), and datum used was WGS84. herpetofauna in Georgia. Collectively, these resources aid Standard English names follow Crother (2012). biologists by helping to identify distributional gaps for which to target survey efforts. Herein we report newly documented county CAUDATA — SALAMANDERS DIRK J. STEVENSON AMBYSTOMA OPACUM (Marbled Salamander). CALHOUN CO.: CHRISTOPHER L. JENKINS 7.8 km W Leary (31.488749°N, 84.595917°W). 18 October 2014. D. KEVIN M. STOHLGREN Stevenson. GMNH 50875. LOWNDES CO.: Langdale Park, Valdosta The Orianne Society, 100 Phoenix Road, Athens, (30.878524°N, 83.317114°W). 3 April 1998. J. Evans. VSU C0015. Georgia 30605, USA First Georgia record for the Suwannee River drainage. MURRAY JOHN B. JENSEN* CO.: Conasauga Natural Area (34.845116°N, 84.848180°W). 12 Georgia Department of Natural Resources, 116 Rum November 2013. N. Klaus and C. Muise. GMNH 50548. Creek Drive, Forsyth, Georgia 31029, USA DAVID L. BECHLER Department of Biology, Valdosta State University, Valdosta, AMBYSTOMA TALPOIDEUM (Mole Salamander). BERRIEN CO.: Georgia 31602, USA St. -
Table 7 - National Wilderness Areas by State
Table 7 - National Wilderness Areas by State * Unit is in two or more States ** Acres estimated pending final boundary determination + Special Area that is part of a proclaimed National Forest State National Wilderness Area NFS Other Total Unit Name Acreage Acreage Acreage Alabama Cheaha Wilderness Talladega National Forest 7,400 0 7,400 Dugger Mountain Wilderness** Talladega National Forest 9,048 0 9,048 Sipsey Wilderness William B. Bankhead National Forest 25,770 83 25,853 Alabama Totals 42,218 83 42,301 Alaska Chuck River Wilderness 74,876 520 75,396 Coronation Island Wilderness Tongass National Forest 19,118 0 19,118 Endicott River Wilderness Tongass National Forest 98,396 0 98,396 Karta River Wilderness Tongass National Forest 39,917 7 39,924 Kootznoowoo Wilderness Tongass National Forest 979,079 21,741 1,000,820 FS-administered, outside NFS bdy 0 654 654 Kuiu Wilderness Tongass National Forest 60,183 15 60,198 Maurille Islands Wilderness Tongass National Forest 4,814 0 4,814 Misty Fiords National Monument Wilderness Tongass National Forest 2,144,010 235 2,144,245 FS-administered, outside NFS bdy 0 15 15 Petersburg Creek-Duncan Salt Chuck Wilderness Tongass National Forest 46,758 0 46,758 Pleasant/Lemusurier/Inian Islands Wilderness Tongass National Forest 23,083 41 23,124 FS-administered, outside NFS bdy 0 15 15 Russell Fjord Wilderness Tongass National Forest 348,626 63 348,689 South Baranof Wilderness Tongass National Forest 315,833 0 315,833 South Etolin Wilderness Tongass National Forest 82,593 834 83,427 Refresh Date: 10/14/2017 -
Herpetological Review: Geographic Distribution
296 GEOGRAPHIC DISTRIBUTION GEOGRAPHIC DISTRIBUTION C AUDATA — SALAMANDERS (2010. Lista Anotada de los Anfibios y Reptiles del Estado de Hi- dalgo, México. Univ. Autó. Estado de Hidalgo, CONABIO, Lito Im- AMBYSTOMA BARBOURI (Streamside Salamander). USA: OHIO: presos Bernal, S. A., Pachuca, Hidalgo, México. x + 104 pp.). The LAWRENCE CO.: Hamilton Township (38.57403°N 82.77565°W, salamander was found in pine-oak forest. WGS84). 21 February 2011. Jeffrey V. Ginger. Verified by Her- M . GUADALUPE LÓPEZ-GARDUÑO (e-mail: guadalupe.bio@hot- man Mays (based on DNA analysis). Cincinnati Museum Center mail.com) and FELIPE RODRÍGUEZ-ROMERO (e-mail: [email protected]), (CMC 12206). New county record (Pfingsten and Matson 2003. Facultad de Ciencias, Universidad Autónoma del Estado de México, Cam- Ohio Salamander Atlas. Ohio Biological Survey Misc. Contribu- pus El Cerrillo, Piedras Blancas, Carretera Toluca – Ixtlahuaca Km. 15.5, To- tion No. 9, Columbus). luca, Edo. de México C.P. 52000. The breeding site was a flooded ditch used as a breeding pool on Back Road. Collected from a ditch that was being used as a EURYCEA CHAMBERLAINI (Chamberlain’s Dwarf Salaman- breeding pool instead of a first or second order stream, the typi- der). USA: ALABAMA: COVINGTON CO.: Conecuh National Forest; cal habitat for the species (Petranka 1998. Salamanders of the Mossy Pond (31.13922°N 86.60119°W; WGS 84). 05 June 2011. C. United States and Canada. Smithsonian Institution Press, Wash- Thawley and S. Graham. Verified by Craig Guyer. AUM 39521. ington, DC. 587 pp.). New county record (Mount 1975. The Reptiles and Amphibians J EFFREY V. -
Amphibian and Reptile Checklist
KEY TO ABBREVIATIONS ___ Eastern Rat Snake (Pantherophis alleghaniensis) – BLUE RIDGE (NC‐C, VA‐C) Habitat: Varies from rocky timbered hillsides to flat farmland. The following codes refer to an animal’s abundance in ___ Eastern Hog‐nosed Snake (Heterodon platirhinos) – PARKWAY suitable habitat along the parkway, not the likelihood of (NC‐R, VA‐U) Habitat: Sandy or friable loam soil seeing it. Information on the abundance of each species habitats at lower elevation. AMPHIBIAN & comes from wildlife sightings reported by park staff and ___ Eastern Kingsnake (Lampropeltis getula) – (NC‐U, visitors, from other agencies, and from park research VA‐U) Habitat: Generalist at low elevations. reports. ___ Northern Mole Snake (Lampropeltis calligaster REPTILE C – COMMON rhombomaculata) – (VA‐R) Habitat: Mixed pine U – UNCOMMON forests and open fields under logs or boards. CHECKLIST R – RARE ___ Eastern Milk Snake (Lampropeltis triangulum) – (NC‐ U, VA‐U) Habitat: Woodlands, grassy balds, and * – LISTED – Any species federally or state listed as meadows. Endangered, Threatened, or of Special Concern. ___ Northern Water Snake (Nerodia sipedon sipedon) – (NC‐C, VA‐C) Habitat: Wetlands, streams, and lakes. Non‐native – species not historically present on the ___ Rough Green Snake (Opheodrys aestivus) – (NC‐R, parkway that have been introduced (usually by humans.) VA‐R) Habitat: Low elevation forests. ___ Smooth Green Snake (Opheodrys vernalis) – (VA‐R) NC – NORTH CAROLINA Habitat: Moist, open woodlands or herbaceous Blue Ridge Red Cope's Gray wetlands under fallen debris. Salamander Treefrog VA – VIRGINIA ___ Northern Pine Snake (Pituophis melanoleucus melanoleucus) – (VA‐R) Habitat: Abandoned fields If you see anything unusual while on the parkway, please and dry mountain ridges with sandier soils. -
Checklist of Amphibians, Reptiles, Birds and Mammals of New York
CHECKLIST OF AMPHIBIANS, REPTILES, BIRDS AND MAMMALS OF NEW YORK STATE Including Their Legal Status Eastern Milk Snake Moose Blue-spotted Salamander Common Loon New York State Artwork by Jean Gawalt Department of Environmental Conservation Division of Fish and Wildlife Page 1 of 30 February 2019 New York State Department of Environmental Conservation Division of Fish and Wildlife Wildlife Diversity Group 625 Broadway Albany, New York 12233-4754 This web version is based upon an original hard copy version of Checklist of the Amphibians, Reptiles, Birds and Mammals of New York, Including Their Protective Status which was first published in 1985 and revised and reprinted in 1987. This version has had substantial revision in content and form. First printing - 1985 Second printing (rev.) - 1987 Third revision - 2001 Fourth revision - 2003 Fifth revision - 2005 Sixth revision - December 2005 Seventh revision - November 2006 Eighth revision - September 2007 Ninth revision - April 2010 Tenth revision – February 2019 Page 2 of 30 Introduction The following list of amphibians (34 species), reptiles (38), birds (474) and mammals (93) indicates those vertebrate species believed to be part of the fauna of New York and the present legal status of these species in New York State. Common and scientific nomenclature is as according to: Crother (2008) for amphibians and reptiles; the American Ornithologists' Union (1983 and 2009) for birds; and Wilson and Reeder (2005) for mammals. Expected occurrence in New York State is based on: Conant and Collins (1991) for amphibians and reptiles; Levine (1998) and the New York State Ornithological Association (2009) for birds; and New York State Museum records for terrestrial mammals. -
Complex Associations of Environmental Factors May Explain Blanchard’S Cricket Frog, Acris Blanchardi Declines and Drive Population Recovery
bioRxiv preprint doi: https://doi.org/10.1101/272161; this version posted August 30, 2018. The copyright holder for this preprint (which was not certified by peer review) is the author/funder. All rights reserved. No reuse allowed without permission. BIORXIV/2018/272161 Complex associations of environmental factors may explain Blanchard’s Cricket Frog, Acris blanchardi declines and drive population recovery. Malcolm L. McCallum1,2 and Stanley E. Trauth3 1P.O. Box 150, Langston, Oklahoma 64040. 2Current Address: Aquatic Resources Center, School of Agriculture & Applied Sciences, E.L. Holloway Agriculture Research, Education, & Extension, Langston University, P.O. Box 1730, Langston, Oklahoma 73050, USA, e-mail: [email protected] 3P.O. Box 599, Department of Biological Sciences, Arkansas State University, State University, Arkansas 72467. Abstract.−Blanchard’s Cricket Frog, Acris blanchardi, is a small hylid frog that was once among the most common amphibians in any part of its range. Today, it remains abundant in much of the southern portion of its range, but is now disappearing elsewhere. Our analysis of habitat characters observed across several states revealed interesting relationships of these factors with the abundance or presence of Blanchard’s Cricket Frog. Further, we later established two ½ acre ponds based on these relationships that led to immediate colonization of the ponds by cricket frogs followed by explosive production of juveniles less than a year later. Our findings suggest that habitat management for this species should specifically manage the shoreline grade and especially the aquatic floating vegetation to maximize population growth and sustenance. Introduction Conservation strategies are impaired when we lack a broad understanding of target’s natural history (Bury 2006; McCallum and McCallum 2006; Gilpin 1986).