Development and Assessment of a Wildlife Habitat Relationship Model for Terrestrial Vertebrates in the State of Maryland
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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. -
Bull Snake Class: Reptilia
Pituophis catenifer sayi Bull Snake Class: Reptilia. Order: Squamata. Family: Colubridae. Other names: Gopher Snake, Pine Snake Physical Description: Bull snakes are usually yellow in color, with brown, black or reddish colored blotching or saddle spots on the sides of the snake. There are dark spots placed between the blotches or saddle spots. Below this is a further row of smaller dark spots. The belly is light brown. Many variations in color have been found, including albinos and white variations. This snake has a small head and a large nose shield, which it uses to dig. They often exceed 6 feet in length, with specimens of up to 100 inches being recorded. Males are generally larger then females. The bull snake is a member of the family of harmless snakes, or Colubridae. This is the largest order of snakes, representing two-thirds of all known snake species. Members of this family are found on all continents except Antarctica, widespread from the Arctic Circle to the southern tips of South America and Africa. All but a handful of species are harmless snakes, not having venom or the ability to deliver toxic saliva through fangs. Most harmless snakes subdue their prey through constriction, striking and seizing small rodents, birds or amphibians and quickly wrapping their body around the prey causing suffocation. While other small species such as the common garter snake lack powers to constrict and feed on only small prey it can overpower. Diet in the Wild: Bull snakes eat small mammals, such as mice, rats, large bugs as well as ground nesting birds, lizards and the young of other snakes. -
Wildlife Diversity Inventory of Maple Springs Wildlife Management Area
Wildlife Diversity Inventory of Maple Springs Wildlife Management Area Josh Campbell, Wildlife Diversity Coordinator Tennessee Wildlife Resources Agency Region 2 TWRA Wildlife Technical Report 14-14 Equal opportunity to participate in and benefit from programs of the Tennessee Wildlife Resources Agency is available to all persons without regard to their race, color, national origin, sex, age, disability, or military service. TWRA is also an equal opportunity/equal access employer. Questions should be directed to TWRA, Human Resources Office, P.O. Box 40747, Nashville, TN 37204, (615) 781-6594 (TDD 781-6691), or to the U.S. Fish and Wildlife Service, Office for Human Resources, 4401 N. Fairfax Dr., Arlington, VA 22203. 2 A small section of open, flooded grassland on Maple Springs Wildlife Management Area attracts waterfowl to the area. 3 Maple Springs Wildlife Management Area (WMA) is located in northeast Coffee County. Although Maple Springs WMA is small, approximately 100 acres, there are a number of differing habitats that include grasslands, forests, and wetlands. Private lands surround the WMA and two of the boundaries are Maple Springs Road and Rigney Road (Figure 1). Both big game and small game hunting occur on the WMA. Big game hunting is limited to the small forest patches occurring on the WMA. Figure 1: Location of Maple Springs WMA. Rabbit hunting is the primary use of the WMA. Once a working farm, the WMA has several ponds and ephemeral wetlands. The forests are mesophytic and there are remnants of Eastern Highland Rim Prairie and Barrens across the WMA. Succession is evident in the old fields. -
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. -
Mercury in Northern Green Frogs and Snapping Turtles from Onondaga Lake, New York
MERCURY IN NORTHERN GREEN FROGS AND SNAPPING TURTLES FROM ONONDAGA LAKE, NEW YORK Prepared by the New York Field Office of the U. S. Fish and Wildlife Service December 2015 For the Onondaga Lake Natural Resource Damage Assessment and Restoration Trustee Council i ABSTRACT This study was conducted to develop an initial understanding of the exposure of amphibians and reptiles at Onondaga Lake to mercury (Hg). Mercury in Onondaga Lake northern green frogs is within the range of Hg concentrations shown to affect metamorphosis and survival of southern leopard frog tadpoles and metamorphs, but less than concentrations associated with effects in wood frogs and American toads. Mercury in the toenails and blood of snapping turtles from Onondaga Lake was significantly higher than Hg in the toenails and blood of Hamlin Wildlife Management Area (reference area) snapping turtles. Onondaga Lake snapping turtles have more Hg in their keratinous tissue (toenails) than other snapping turtles sampled across New York State, but less Hg than found in keratinous tissues of snapping turtles from a Hg-contaminated area in Virginia. Snapping turtles appear fairly resistant to Hg, but the Hg concentrations found in Onondaga Lake snapping turtles are within the range of concentrations associated with altered thyroid function and immune suppression in other turtle species. Although the diversity of amphibians and reptiles has increased at Onondaga Lake over the past two decades, the herpetofaunal diversity and population densities remain lower than in surrounding areas. This study shows that Hg may be a factor inhibiting the reproduction and health of some amphibians and reptiles at Onondaga Lake. -
Deicing Salts Influence Ranavirus Outbreaks in Wood Frog (Lithobates Sylvaticus) Tadpoles Sarah Jacobson [email protected]
University of Connecticut OpenCommons@UConn Honors Scholar Theses Honors Scholar Program Spring 5-2-2019 Deicing Salts Influence Ranavirus Outbreaks in Wood Frog (Lithobates sylvaticus) Tadpoles Sarah Jacobson [email protected] Follow this and additional works at: https://opencommons.uconn.edu/srhonors_theses Part of the Animal Diseases Commons, Animal Experimentation and Research Commons, Biodiversity Commons, Population Biology Commons, Terrestrial and Aquatic Ecology Commons, and the Virus Diseases Commons Recommended Citation Jacobson, Sarah, "Deicing Salts Influence Ranavirus Outbreaks in Wood Frog (Lithobates sylvaticus) Tadpoles" (2019). Honors Scholar Theses. 618. https://opencommons.uconn.edu/srhonors_theses/618 Jacobson 1 Deicing Salts Influence Ranavirus Outbreaks in Wood Frog (Lithobates sylvaticus) Tadpoles Sarah K. Jacobson Department of Natural Resources and the Environment, Center for Wildlife and Fisheries Conservation Center, University of Connecticut Tracy A. G. Rittenhouse Department of Natural Resources and the Environment, Center for Wildlife and Fisheries Conservation Center, University of Connecticut Jacobson 2 Abstract Ecosystems are increasingly being exposed to anthropogenic stressors that could make animals and thus populations more susceptible to disease. For example, the application of deicing salts to roads is increasing in the northeastern United States. Chronic stress that larval amphibians experience when living in vernal pools with high salinity may alter their susceptibility to ranavirus, a pathogen responsible for mass mortality events worldwide. This project quantifies the effects of road salts and ranavirus exposure on larval wood frog (Lithobates sylvaticus) growth and survival. Using outdoor mesocsoms, we raised wood frog tadpoles in salt treatments and then exposed them to the FV3 strain of ranavirus, with the hypothesis that individuals raised in salt treatments would have lower survival, and metamorph earlier at larger size when exposed to ranavirus than those from no salt treatments. -
TPWD White List
TPWD White List Frogs and Toads Great Plains toad (Bufo cognatus) Green toad (Bufo debilis) Red-spotted toad (Bufo punctatus) Texas toad (Bufo speciosus) Gulf Coast toad (Bufo valliceps) Woodhouse’s toad (Bufo woodhousei) Green treefrog (Hyla cinerea) Bull frog (Rana catesbeiana) Couch’s spadefoot (Scaphiopus couchii) Plains spadefoot (Spea bombifrons) New Mexico spadefoot (Spea multiplicata) Salamanders Tiger salamander (Ambystoma tigrinum) Lizards Green anole (Anolis carolinensis) Chihuahuan spotted whiptail (Aspidoscelis exsanguis) Texas spotted whiptail (Aspidoscelis gularis) Marbled whiptail (Aspidoscelis marmoratus) Six-lined racerunner (Aspidoscelis sexlineatus) Checkered whiptail (Aspidoscelis tesselatus) Texas banded gecko (Coleonyx brevis) Greater earless lizard (Cophosaurus texanus) Collared lizard (Crotaphytus collaris) Five-lined skink (Eumeces fasciatus) Great plains skink (Eumeces obsoletus) Texas alligator lizard (Gerrhonotus infernalis) Lesser earless lizard (Holbrookia maculata) Crevice spiny lizard (Sceloporus poinsettii) Prairie lizard (Sceloporus undulatus) Ground skink (Scincella lateralis) Tree lizard (Urosaurus ornatus) Side-blotched lizard (Uta stansburiana) Snakes Copperhead (Agkistrodon contortrix) Cottonmouth (Agkistrodon piscivorus) Glossy snake (Arizona elegans) Trans-Pecos rat snake (Bogertophis subocularis) Racer (Coluber constrictor) Western diamondback rattlesnake (Crotalus atrox) Rock rattlesnake (Crotalus lepidus) Blacktail rattlesnake (Crotalus molossus) Mojave rattlesnake (Crotalus scutulatus) Prairie -
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 ................................................................................................................................ -
Snakes of the Everglades Agricultural Area1 Michelle L
CIR1462 Snakes of the Everglades Agricultural Area1 Michelle L. Casler, Elise V. Pearlstine, Frank J. Mazzotti, and Kenneth L. Krysko2 Background snakes are often escapees or are released deliberately and illegally by owners who can no longer care for them. Snakes are members of the vertebrate order Squamata However, there has been no documentation of these snakes (suborder Serpentes) and are most closely related to lizards breeding in the EAA (Tennant 1997). (suborder Sauria). All snakes are legless and have elongated trunks. They can be found in a variety of habitats and are able to climb trees; swim through streams, lakes, or oceans; Benefits of Snakes and move across sand or through leaf litter in a forest. Snakes are an important part of the environment and play Often secretive, they rely on scent rather than vision for a role in keeping the balance of nature. They aid in the social and predatory behaviors. A snake’s skull is highly control of rodents and invertebrates. Also, some snakes modified and has a great degree of flexibility, called cranial prey on other snakes. The Florida kingsnake (Lampropeltis kinesis, that allows it to swallow prey much larger than its getula floridana), for example, prefers snakes as prey and head. will even eat venomous species. Snakes also provide a food source for other animals such as birds and alligators. Of the 45 snake species (70 subspecies) that occur through- out Florida, 23 may be found in the Everglades Agricultural Snake Conservation Area (EAA). Of the 23, only four are venomous. The venomous species that may occur in the EAA are the coral Loss of habitat is the most significant problem facing many snake (Micrurus fulvius fulvius), Florida cottonmouth wildlife species in Florida, snakes included. -
Biological Resources and Management
Vermilion flycatcher The upper Muddy River is considered one of the Mojave’s most important Common buckeye on sunflower areas of biodiversity and regionally Coyote (Canis latrans) Damselfly (Enallagma sp.) (Junonia coenia on Helianthus annuus) important ecological but threatened riparian landscapes (Provencher et al. 2005). Not only does the Warm Springs Natural Area encompass the majority of Muddy River tributaries it is also the largest single tract of land in the upper Muddy River set aside for the benefit of native species in perpetuity. The prominence of water in an otherwise barren Mojave landscape provides an oasis for regional wildlife. A high bird diversity is attributed to an abundance of riparian and floodplain trees and shrubs. Contributions to plant diversity come from the Mojave Old World swallowtail (Papilio machaon) Desertsnow (Linanthus demissus) Lobe-leaved Phacelia (Phacelia crenulata) Cryptantha (Cryptantha sp.) vegetation that occur on the toe slopes of the Arrow Canyon Range from the west and the plant species occupying the floodplain where they are supported by a high water table. Several marshes and wet meadows add to the diversity of plants and animals. The thermal springs and tributaries host an abundance of aquatic species, many of which are endemic. The WSNA provides a haven for the abundant wildlife that resides permanently or seasonally and provides a significant level of protection for imperiled species. Tarantula (Aphonopelma spp.) Beavertail cactus (Opuntia basilaris) Pacific tree frog (Pseudacris regilla) -
Ecology of Upland Snake Communities in Managed Montane Longleaf Pine Habitats of Georgia Miranda Gulsby Kennesaw State University
Kennesaw State University DigitalCommons@Kennesaw State University Department of Ecology, Evolution, and Organismal Master of Science in Integrative Biology Theses Biology Summer 7-25-2019 Ecology of Upland Snake Communities in Managed Montane Longleaf Pine Habitats of Georgia Miranda Gulsby Kennesaw State University Follow this and additional works at: https://digitalcommons.kennesaw.edu/integrbiol_etd Part of the Integrative Biology Commons, and the Terrestrial and Aquatic Ecology Commons Recommended Citation Gulsby, Miranda, "Ecology of Upland Snake Communities in Managed Montane Longleaf Pine Habitats of Georgia" (2019). Master of Science in Integrative Biology Theses. 48. https://digitalcommons.kennesaw.edu/integrbiol_etd/48 This Thesis is brought to you for free and open access by the Department of Ecology, Evolution, and Organismal Biology at DigitalCommons@Kennesaw State University. It has been accepted for inclusion in Master of Science in Integrative Biology Theses by an authorized administrator of DigitalCommons@Kennesaw State University. For more information, please contact [email protected]. Ecology of Upland Snake Communities in Managed Montane Longleaf Pine Habitats of Georgia Miranda Louise Gulsby A Thesis Presented in Partial Fulfillment of Requirements of the Master of Science in Integrative Biology for the Department of Evolution, Ecology, and Organismal Biology Kennesaw State University 1000 Chastain Road Kennesaw, Ga 30144 July 2019 Major Advisor: Thomas McElroy, Ph. D. Committee Members: Joel McNeal, Ph.