Veterans Park Herpetological Report Manning 2015
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Queen Snake, Regina Septemvittata
Queen Snake, Regina septemvittata Status: State: Endangered Federal: Not listed Identification This slender snake can reach lengths of 16-24 in. (41-61 cm) when fully grown. The dorsal (or upper) surface of a queen snake is a solid, grayish-brown color. A yellow band is present on the lower half of the body and extends from the snake’s chin to its tail. The belly of the snake is a white to yellow color with four characteristic stripes that make for easy identification. Of these four stripes, the two outer stripes are visibly thicker than the inner pair. Queen snakes have keeled scales and an © Rudolf G. Arndt anal plate that is divided. Habitat This species is highly aquatic and a very adept swimmer. Authorities report that swiftly flowing creeks, brooks and streams are the preferred habitat for queen snakes (Wright and Wright 1957). But finding them along the edges of more slowly flowing rivers and streams, and sometimes lakes, is not uncommon in some states. The queen snake’s diet (see below) always keeps it close to water, where it can sometimes be seen with just its head above the surface of the water. On occasion, a lucky observer might find these snakes basking in high numbers along the banks of streams and even hanging from streamside vegetation (Golden, personal observation). Such aggregations are probably unlikely in New Jersey, however. The best strategy for finding this species in the state would be to look under flat rocks and other debris along the banks of the Delaware River and its tributaries. -
Mitochondrial Discordance and Gene Flow in a Recent Radiation of Toads
Molecular Phylogenetics and Evolution 59 (2011) 66–80 Contents lists available at ScienceDirect Molecular Phylogenetics and Evolution journal homepage: www.elsevier.com/locate/ympev Nuclear–mitochondrial discordance and gene flow in a recent radiation of toads ⇑ Brian E. Fontenot , Robert Makowsky 1, Paul T. Chippindale Department of Biology, University of Texas at Arlington, Arlington, TX 76019, United States article info abstract Article history: Natural hybridization among recently diverged species has traditionally been viewed as a homogenizing Received 28 April 2010 force, but recent research has revealed a possible role for interspecific gene flow in facilitating species Revised 12 December 2010 radiations. Natural hybridization can actually contribute to radiations by introducing novel genes or Accepted 23 December 2010 reshuffling existing genetic variation among diverging species. Species that have been affected by natural Available online 19 January 2011 hybridization often demonstrate patterns of discordance between phylogenies generated using nuclear and mitochondrial markers. We used Amplified Fragment Length Polymorphism (AFLP) data in conjunc- Keywords: tion with mitochondrial DNA in order to examine patterns of gene flow and nuclear–mitochondrial dis- Toads cordance in the Anaxyrus americanus group, a recent radiation of North American toads. We found high Hybridization Gene flow levels of gene flow between putative species, particularly in species pairs sharing similar male advertise- Speciation ment calls that occur in close geographic proximity, suggesting that prezygotic reproductive isolating AFLPs mechanisms and isolation by distance are the primary determinants of gene flow and genetic differenti- Nuclear–mitochondrial discordance ation among these species. Additionally, phylogenies generated using AFLP and mitochondrial data were markedly discordant, likely due to recent and/or ongoing natural hybridization events between sympatric populations. -
Distribution of the Queen Snake (Regina Septemvittata) in Arkansas Johnathan W
Journal of the Arkansas Academy of Science Volume 61 Article 17 2007 Distribution of the Queen Snake (Regina septemvittata) in Arkansas Johnathan W. Stanley Arkansas State University, [email protected] Stanley E. Trauth Arkansas State University Follow this and additional works at: http://scholarworks.uark.edu/jaas Part of the Zoology Commons Recommended Citation Stanley, Johnathan W. and Trauth, Stanley E. (2007) "Distribution of the Queen Snake (Regina septemvittata) in Arkansas," Journal of the Arkansas Academy of Science: Vol. 61 , Article 17. Available at: http://scholarworks.uark.edu/jaas/vol61/iss1/17 This article is available for use under the Creative Commons license: Attribution-NoDerivatives 4.0 International (CC BY-ND 4.0). Users are able to read, download, copy, print, distribute, search, link to the full texts of these articles, or use them for any other lawful purpose, without asking prior permission from the publisher or the author. This Article is brought to you for free and open access by ScholarWorks@UARK. It has been accepted for inclusion in Journal of the Arkansas Academy of Science by an authorized editor of ScholarWorks@UARK. For more information, please contact [email protected], [email protected]. Journal of the Arkansas Academy of Science, Vol. 61 [2007], Art. 17 -I Distribution of the Queen Snake (Regina septemvittata) in Arkansas llinOiS./ JONATHAN W. STANLEyl,2 AND STANLEY E. TRAUTH1 ~orgia. lDepartment ofBiological Sciences, Arkansas State University, PO Box 599, State University, AR 72467-0599 rabbi! NOods /. torrespondence: [email protected] I [MS , i ~rslty. I Abstract.-We documented the distribution ofthe queen snake, Regina septemvittata, in northern Arkansas during the 2005 and 2006 activity seasons. -
Checklist Reptile and Amphibian
To report sightings, contact: Natural Resources Coordinator 980-314-1119 www.parkandrec.com REPTILE AND AMPHIBIAN CHECKLIST Mecklenburg County, NC: 66 species Mole Salamanders ☐ Pickerel Frog ☐ Ground Skink (Scincella lateralis) ☐ Spotted Salamander (Rana (Lithobates) palustris) Whiptails (Ambystoma maculatum) ☐ Southern Leopard Frog ☐ Six-lined Racerunner ☐ Marbled Salamander (Rana (Lithobates) sphenocephala (Aspidoscelis sexlineata) (Ambystoma opacum) (sphenocephalus)) Nonvenomous Snakes Lungless Salamanders Snapping Turtles ☐ Eastern Worm Snake ☐ Dusky Salamander (Desmognathus fuscus) ☐ Common Snapping Turtle (Carphophis amoenus) ☐ Southern Two-lined Salamander (Chelydra serpentina) ☐ Scarlet Snake1 (Cemophora coccinea) (Eurycea cirrigera) Box and Water Turtles ☐ Black Racer (Coluber constrictor) ☐ Three-lined Salamander ☐ Northern Painted Turtle ☐ Ring-necked Snake (Eurycea guttolineata) (Chrysemys picta) (Diadophis punctatus) ☐ Spring Salamander ☐ Spotted Turtle2, 6 (Clemmys guttata) ☐ Corn Snake (Pantherophis guttatus) (Gyrinophilus porphyriticus) ☐ River Cooter (Pseudemys concinna) ☐ Rat Snake (Pantherophis alleghaniensis) ☐ Slimy Salamander (Plethodon glutinosus) ☐ Eastern Box Turtle (Terrapene carolina) ☐ Eastern Hognose Snake ☐ Mud Salamander (Pseudotriton montanus) ☐ Yellow-bellied Slider (Trachemys scripta) (Heterodon platirhinos) ☐ Red Salamander (Pseudotriton ruber) ☐ Red-eared Slider3 ☐ Mole Kingsnake Newts (Trachemys scripta elegans) (Lampropeltis calligaster) ☐ Red-spotted Newt Mud and Musk Turtles ☐ Eastern Kingsnake -
American Toad (Anaxyrus Americanus) Fowler's Toad (Anaxyrus Fowleri
Vermont has eleven known breeding species of frogs. Their exact distributions are still being determined. In order for these species to survive and flourish, they need our help. One way you can help is to report the frogs that you come across in the state. Include in your report as much detail as you can on the appearance and location of the animal; also include the date of the sighting, your name, and how to contact you. Photographs are ideal, but not necessary. When attempting to identify a particular species, check at least three different field markings so that you can be sure of what it is. To contribute a report, you may use our website (www.vtherpatlas.org) or contact Jim Andrews directly at [email protected]. American Bullfrog (Lithobates catesbeianus) American Toad (Anaxyrus americanus) The American Bullfrog is our largest frog and can reach 7 inches long. The Bullfrog is one of the three The American Toad is one of Vermont’s two toad species. Toads can be distinguished from other green-faced frogs in Vermont. It has a green and brown mottled body with dark stripes across its legs. frogs in Vermont by their dry and bumpy skin, and the long oval parotoid glands on each side of their The Bullfrog does not have dorsolateral ridges, but it does have a ridge that starts at the eye and goes necks. The American Toad has at least one large wart in each of the large black spots found along its around the eardrum (tympana) and down. The Bullfrog’s call is a deep low jum-a-rum. -
Annotated Checklist of Amphibian and Reptile Species Observed at the Gordon Natural Area (West Chester University, PA) 2008-2020
West Chester University Digital Commons @ West Chester University Gordon Natural Area Biodiversity Studies Documents Gordon Natural Area Biodiversity Studies 7-28-2020 Annotated Checklist of Amphibian and Reptile Species Observed at the Gordon Natural Area (West Chester University, PA) 2008-2020. Version I Nur Ritter Harry Tiebout Follow this and additional works at: https://digitalcommons.wcupa.edu/gna_bds_series Part of the Biodiversity Commons Annotated Checklist of Amphibian and Reptile Species Observed at the Gordon Natural Area (West Chester University, PA) 2008-2020. Version I Summary Data Number of Taxa: Species, in 14 Genera, 6 Families, and 4 Orders. Description Data were compiled from surveys by Dr. Harry Tiebout, augmented by observations from GNA staff (which, as used here, includes student interns), graduate student Steven Clay, the Stroud Water Research Center, additional WCU Faculty, and members of the WCU Grounds Department. Local residents who are regular visitors to the Gordon have also occasionally contributed observations. Because herptile data haven't been systematically archived by the GNA staff until recent years, there are many gaps in the observation timeline that are clearly artificial. For example, although the observation history for the Eastern American Toad, Eastern Redback Salamander, and Eastern Box Turtle suggests that there were a number of years in which one, or all, of these species were not seen at the GNA, it is very likely that all three of these species have been observed numerous times during every year that the GNA has been in existence. Hopefully, moving forward, we'll be able to maintain a more complete record of observations. -
Response of Reptile and Amphibian Communities to the Reintroduction of Fire T in an Oak/Hickory Forest ⁎ Steven J
Forest Ecology and Management 428 (2018) 1–13 Contents lists available at ScienceDirect Forest Ecology and Management journal homepage: www.elsevier.com/locate/foreco Response of reptile and amphibian communities to the reintroduction of fire T in an oak/hickory forest ⁎ Steven J. Hromadaa, , Christopher A.F. Howeyb,c, Matthew B. Dickinsond, Roger W. Perrye, Willem M. Roosenburgc, C.M. Giengera a Department of Biology and Center of Excellence for Field Biology, Austin Peay State University, Clarksville, TN 37040, United States b Biology Department, University of Scranton, Scranton, PA 18510, United States c Ohio Center for Ecology and Evolutionary Studies, Department of Biological Sciences, Ohio University, Athens, OH 45701, United States d Northern Research Station, U.S. Forest Service, Delaware, OH 43015, United States e Southern Research Station, U.S. Forest Service, Hot Springs, AR 71902, United States ABSTRACT Fire can have diverse effects on ecosystems, including direct effects through injury and mortality and indirect effects through changes to available resources within the environment. Changes in vegetation structure suchasa decrease in canopy cover or an increase in herbaceous cover from prescribed fire can increase availability of preferred microhabitats for some species while simultaneously reducing preferred conditions for others. We examined the responses of herpetofaunal communities to prescribed fires in an oak/hickory forest in western Kentucky. Prescribed fires were applied twice to a 1000-ha area one and four years prior to sampling, causing changes in vegetation structure. Herpetofaunal communities were sampled using drift fences, and vegetation attributes were sampled via transects in four burned and four unburned plots. Differences in reptile community structure correlated with variation in vegetation structure largely created by fires. -
Field Guide Field Journal Blanchard's Cricket Frog
Field Guide Frogs and Toads of the Washington, D.C. Area Field Journal Name: Date: Blanchard's cricket frog Location: Acris crepitans Baird, 1854 Weather: Time of Day: Observations / Data / Activity Overview General Description Acris crepitans is 1.6-3.5 cm long and has a blunt, pointed head with an occasional triangular marking. Its back and legs are covered with various dark markings. It has a middorsal bright green or brown stripe and the rear of its thigh has a distinct ragged dark stripe. A white bar extends from its eye to its foreleg. The body is slim-waisted and small while the skin is granular and warty. Hind toes are extensively webbed and toe pads are poorly developed (Stebbins 2003). Acris crepitans paludicola and Acris crepitans blanchardi are recognized as subspecies. A. c. paludicola has smooth skin with a pinkish patterned coloration. The throat Write down questions that you have for further exploration. remains pink, even for males during breeding season. A. c. blanchardi by comparison is wartier, bulkier, and heavier with a light brown or gray uniform coloration (Conant and Collins 1991). Males have more ventral spotting than females (Stebbins 2003). Distribution Unlike most small frogs in its range, A. c. crepitans does not leave the vicinity of water in its adult stage. It is found at the edge of ponds and slow-moving streams, tending to avoid wooded areas and dense vegetation (Hulse McCoy and Censky 2001). A. c. blanchardi is found in Michigan, Ohio, Nebraska, eastern Colorado, and most of Texas. A few have been spotted in Minnesota and New Mexico as well. -
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. -
Fisheries Order 224.21 Regulations on the Take of Reptiles and Amphibians
FO-224.21 FISHERIES ORDER Regulations on the Take of Reptiles and Amphibians Order 224.21 By authority conferred on the Natural Resources Commission and the Department of Natural Resources by Part 487 of 1994 PA 451, MCL 324.48701 to 324.48740, ordered on October 8, 2020, the following section(s) of the Fisheries Order shall read effective April 1, 2021, except as otherwise provided: It shall be unlawful to kill, take, trap, possess, buy, sell, offer to buy or sell, barter, or attempt to take, trap, possess or barter any reptile or amphibian from the wild, or the eggs of any reptile or amphibian from the wild, except as provided within this order. GENERAL 1. The following species of reptiles and amphibians shall not be taken from the wild and possessed except as authorized under a permit for scientific research, conservation, or educational purposes from the director: Eastern massasauga rattlesnake (Sistrurus catenatus catenatus) Queen snake (Regina septemvittata) Grey rat snake (Pantherophis spiloides) [formerly known as the Black rat snake (Elaphe obsoleta obsoleta)] – exception: albino color variations of this species commonly bred in the pet trade may be possessed without permit Butler’s garter snake (Thamnophis butleri) Smooth green snake (Opheodrys vernalis) [= Liochlorophis vernalis} Blanding's turtle (Emydoidea blandingii) Wood turtle (Glyptemys insculpta) Eastern box turtle (Terrapene carolina) Boreal chorus frog (Pseudarcris maculata) Mink frog (Rana septentrionalis) Pickerel frog (Rana palustris) Fowler’s toad (Bufo [Anaxyrus]fowleri) [= Bufo woodhousii fowleri] Mudpuppy (Necturus maculosus) Northern two-lined salamander (Eurycea bisleneata) Northern dusky salamander (Desmognathus fuscus) Western lesser siren (Siren intermedia nettingi) 2. -
Frogs and Toads of the Atchafalaya Basin
Frogs and Toads of the Atchafalaya Basin True Toads (Family Bufonidae) Microhylid Frogs and Toads Two true toads occur in the Atchafalaya Basin: (Family Microhylidae) True Toads Fowler’s Toad and the Gulf Coast Toad. Both The Eastern Narrow-Mouthed Toad is the Microhylid Frogs and Toads of these species are moderately sized and have only representative in the Atchafalaya Basin dry, warty skin. They have short hind limbs of this family. It is a plump frog with smooth and do not leap like other frogs, but rather skin, a pointed snout, and short limbs. There they make short hops to get around. They are is a fold of skin across the back of the head active primarily at night and use their short that can be moved forward to clear the hind limbs for burrowing into sandy soils eyes. They use this fold of skin especially during the day. They are the only two frogs when preying upon ants, a favorite food, to in the basin that lay long strings of eggs, as remove any attackers. Because of its plump opposed to clumps laid by other frog species. body and short limbs the male must secrete a Fowler’s Toad Gulf Coast Toad Both of these toad species possess enlarged sticky substance from a gland on its stomach Eastern Narrow-Mouthed Toad (Anaxyrus fowleri ) (Incilius nebulifer) glands at the back of the head that secrete a to stay attached to a female for successful (Gastrophryne carolinensis) white poison when attacked by a predator. mating; in most other frogs, the limbs are When handling these toads, one should avoid long enough to grasp around the female. -
Venomous Nonvenomous Snakes of Florida
Venomous and nonvenomous Snakes of Florida PHOTOGRAPHS BY KEVIN ENGE Top to bottom: Black swamp snake; Eastern garter snake; Eastern mud snake; Eastern kingsnake Florida is home to more snakes than any other state in the Southeast – 44 native species and three nonnative species. Since only six species are venomous, and two of those reside only in the northern part of the state, any snake you encounter will most likely be nonvenomous. Florida Fish and Wildlife Conservation Commission MyFWC.com Florida has an abundance of wildlife, Snakes flick their forked tongues to “taste” their surroundings. The tongue of this yellow rat snake including a wide variety of reptiles. takes particles from the air into the Jacobson’s This state has more snakes than organs in the roof of its mouth for identification. any other state in the Southeast – 44 native species and three nonnative species. They are found in every Fhabitat from coastal mangroves and salt marshes to freshwater wetlands and dry uplands. Some species even thrive in residential areas. Anyone in Florida might see a snake wherever they live or travel. Many people are frightened of or repulsed by snakes because of super- stition or folklore. In reality, snakes play an interesting and vital role K in Florida’s complex ecology. Many ENNETH L. species help reduce the populations of rodents and other pests. K Since only six of Florida’s resident RYSKO snake species are venomous and two of them reside only in the northern and reflective and are frequently iri- part of the state, any snake you en- descent.