Abstracts of Papers Presented at the Nineteenth Annual Meeting of the Mha
Total Page:16
File Type:pdf, Size:1020Kb
Load more
Recommended publications
-
Nonnative Reptilies in South Florida ID Guide
Nonnative Reptiles in South Florida Identification Guide • The nonnative reptiles shown here are native to Central and South America, Asia, and Nonnative species are Africa. They were introduced to south Florida by human activity. sometimes confused with • Invasive species harm native species through direct predation, competition for resources, the Florida natives shown spread of disease, and disruption of natural ecosystems. Many of the nonnative reptiles on because their colorations this guide are, or have the potential to become, invasive. and patterns are very • Use this guide to identify invasive species and immediately report sightings of the black similar. Pay attention to the and white tegu, Nile monitor, and all invasive snakes to 1-888-IVE-GOT1. Take a distinct characteristics and photo and note the location relative to street intersections or with a GPS if possible. typical adult sizes listed on this guide to avoid • More photos can be found at www.flmnh.ufl.edu/herpetology/herpetology.htm. confusion when you • Be certain that an animal is a nonnative species before removing it. Warning-most encounter these animals. reptiles will bite or scratch if provoked. Nonnative Lizards NATIVE :- • ,,.., •· t ..... Look-a-Likes . ... ·-tt-..... • •. .. l . 1 '\..\ =- ' . ----.....·~·-· - - ',-<•'-' ' . \:,' . <! •.t'- . ,. '\. Dav id 13,irbsv ~ ·- ~ 9111'.', o:'"' w:' Black and White Tegu 2 to 3 ft. Dark bands with plentiful white dots between them Eastern Fence Lizard 3.5 to 7.5 in. Northern Curly-Tailed Lizard 7 to 10.5 in . Gray to tan with curled tail Florida Scrub Lizard 3.5 to 5.5 in. American Alligator 6 to 9 ft. Nile Monitor 4 to 6 ft. -
Yellow-Bellied Water Snake Plain-Bellied Water
Nature Flashcards Snakes All photos are subject to the terms of the Creative Commons Public License Based on Nature Quiz Attribution-Non-Commercial 3.0 United States unless copyright otherwise By Phil Huxford noted. TMN-COT Meeting November, 2013 Texas Master Naturalist Cradle of Texas Chapter Cradle of Texas Chapter Yellow-bellied Water Snake Plain-bellied Water Snake Nerodia erythrogaster flavigaster Elliptical eye pupils Bright yellow underneath Found around ponds, lakes, swamps, and wet bottomland forests 2 – 3 feet long Cradle of Texas Chapter Broad-banded Water snake Nerodia fasciata confluens Dark, wide bands separated by yellow Bold, dark checked stripes Strong swimmer Cradle of Texas Chapter 2 – 4 feet long Blotched Water Snake Nerodia erythrogaster transversa Black-edged; dark brown dorsal markings Yellow or sometimes orange belly Lives in small ponds, ditches, and rain-filled pools Typically 2 – 5 feet long Cradle of Texas Chapter Diamond-back Water Snake Northern Diamond-back Water Snake Nerodia rhombifer Heavy-bodied, large girth Can be dark brown Head somewhat flattened and wide Texas’ largest Nerodia Strikes without warning and viciously 4 – 6’ long Cradle of Texas Chapter Photo by J.D. Wilson http://srelherp.uga.edu/snakes/ Western Mud Snake Mud Snake Farancia abacura Lives in our area but rarely seen Glossy black above Red belly with black lines in belly Found in wooded swampland and wet areas Does not bite when handled but pokes tail like stinger 3 – 4 feet long Cradle of Texas Chapter Texas Coral Snake Micrurus fulvius tenere Blunt head; shiny, slender body Round pupils Colors red, yellow, black Lives in partly wooded organic material Cradle of Texas Chapter Usually 2 – 3 feet long Record: 47 ¾ inches in Brazoria County ‘Red touches yellow – kill a fellow. -
Amphibians Present in the Barataria Preserve of Jean Lafitte National Historical Park and Preserve
Amphibians present in the Barataria Preserve of Jean Lafitte National Historical Park and Preserve. The species list was generated from data compiled from NPS observations and during a 2001-2002 reptile and amphibian inventory conducted by Noah J. Anderson and Dr. Richard A. Seigel, Southeastern Louisiana University, Hammond, Louisiana. Common Name Scientific Name Habitat Association Smallmouth salamander Ambystoma texanum hardwood forests Three-toed amphiuma Amphiuma tridactylum swamp, marsh, restricted to aquatic habitats in hardwood forests Dwarf salamander Eurycea quadridigitata hardwood forests, marsh Eastern newt Notophthalmus viridescens found in and near aquatic habitats Southern dusky salamander Desmognathus auriculatus hardwood forests Lesser siren Siren intermedia swamp, marsh Northern cricket frog Acris crepitans all habitats Gulf coast toad Bufo valliceps all habitats Greenhouse frog Eleutherodactylus planirostris hardwood forests Eastern narrowmouth toad Gastrophryne carolinensis all habitats Bird-voiced treefrog Hyla avivoca hardwood forests, swamp Green treefrog Hyla cinerea all habitats Squirrel treefrog Hyla squirella swamp, hardwood forests Spring peeper Pseudacris crucifer swamp, hardwood forests Chorus frog Pseudacris triseriata hardwood forests, swamp Bullfrog Rana catesbeiana hardwood forests, swamp Bronze frog Rana clamitans all habitats Pig frog Rana grylio marsh Southern leopard frog Rana sphenocephala swamp, marsh Reptiles present in the Barataria Preserve of Jean Lafitte National Historical Park and Preserve. -
Hybridization Between Multiple Fence Lizard Lineages in an Ecotone
Molecular Ecology (2007) 16, 1035–1054 doi: 10.1111/j.1365-294X.2006.03194.x HybridizationBlackwell Publishing Ltd between multiple fence lizard lineages in an ecotone: locally discordant variation in mitochondrial DNA, chromosomes, and morphology ADAM D. LEACHÉ* and CHARLES J. COLE†‡ *Museum of Vertebrate Zoology and Department of Integrative Biology, 3101 Valley Life Sciences Building, University of California, Berkeley, CA 94720-3160, USA, †Department of Herpetology, American Museum of Natural History, New York, NY 10024-5192, USA Abstract We investigated a hybrid zone between two major lineages of fence lizards (Sceloporus cowlesi and Sceloporus tristichus) in the Sceloporus undulatus species complex in eastern Arizona. This zone occurs in an ecotone between Great Basin Grassland and Conifer Wood- land habitats. We analysed spatial variation in mtDNA (N = 401; 969 bp), chromosomes (N = 217), and morphology (N = 312; 11 characters) to characterize the hybrid zone and assess species limits. A fine-scale population level phylogenetic analysis refined the boundaries between these species and indicated that four nonsister mtDNA clades (three belonging to S. tristichus and one to S. cowlesi) are sympatric at the centre of the zone. Esti- mates of cytonuclear disequilibria in the population closest to the centre of the hybrid zone suggest that the S. tristichus clades are randomly mating, but that the S. cowlesi haplotype has a significant nonrandom association with nuclear alleles. Maximum-likelihood cline- fitting analyses suggest that the karyotype, morphology, and dorsal colour pattern clines are all coincident, but the mtDNA cline is skewed significantly to the south. A temporal comparison of cline centres utilizing karyotype data collected in the early 1970s and in 2002 suggests that the cline may have shifted by approximately 1.5 km to the north over a 30-year period. -
Check List 17 (1): 27–38
17 1 ANNOTATED LIST OF SPECIES Check List 17 (1): 27–38 https://doi.org/10.15560/17.1.27 A herpetological survey of Edith L. Moore Nature Sanctuary Dillon Jones1, Bethany Foshee2, Lee Fitzgerald1 1 Biodiversity Research and Teaching Collections, Department of Ecology and Conservation Biology, Texas A&M University, College Station, TX, USA. 2 Houston Audubon, 440 Wilchester Blvd. Houston, TX 77079 USA. Corresponding author: Dillon Jones, [email protected] Abstract Urban herpetology deals with the interaction of amphibians and reptiles with each other and their environment in an ur- ban setting. As such, well-preserved natural areas within urban environments can be important tools for conservation. Edith L. Moore Nature Sanctuary is an 18-acre wooded sanctuary located west of downtown Houston, Texas and is the headquarters to Houston Audubon Society. This study compared iNaturalist data with results from visual encounter surveys and aquatic funnel traps. Results from these two sources showed 24 species belonging to 12 families and 17 genera of herpetofauna inhabit the property. However, several species common in surrounding areas were absent. Combination of data from community science and traditional survey methods allowed us to better highlight herpe- tofauna present in the park besides also identifying species that may be of management concern for Edith L. Moore. Keywords Community science, iNaturalist, urban herpetology Academic editor: Luisa Diele-Viegas | Received 27 August 2020 | Accepted 16 November 2020 | Published 6 January 2021 Citation: Jones D, Foshee B, Fitzgerald L (2021) A herpetology survey of Edith L. Moore Nature Sanctuary. Check List 17 (1): 27–28. https://doi. -
The Southern Watersnake (Nerodia Fasciata) in Folsom, California: History, Population Attributes, and Relation to Other Introduced Watersnakes in North America
THE SOUTHERN WATERSNAKE (NERODIA FASCIATA) IN FOLSOM, CALIFORNIA: HISTORY, POPULATION ATTRIBUTES, AND RELATION TO OTHER INTRODUCED WATERSNAKES IN NORTH AMERICA FINAL REPORT TO: U. S. Fish and Wildlife Service Sacramento Fish and Wildlife Office 2800 Cottage Way, Room W-2605 Sacramento, California 95825-1846 UNDER COOPERATIVE AGREEMENT #11420-1933-CM02 BY: ECORP Consulting, Incorporated 2260 Douglas Blvd., Suite 160 Roseville, California 95661 Eric W. Stitt, M. S., University of Arizona, School of Natural Resources, Tucson Peter S. Balfour, M. S., ECORP Consulting Inc., Roseville, California Tara Luckau, University of Arizona, Dept. of Ecology and Evolution, Tucson Taylor E. Edwards, M. S., University of Arizona, Genomic Analysis and Technology Core The Southern Watersnake (Nerodia fasciata) in Folsom, California: History, Population Attributes, and Relation to Other Introduced Watersnakes in North America CONTENTS INTRODUCTION ...............................................................................................................1 The Southern Watersnake (Nerodia fasciata)................................................................3 Study Area ....................................................................................................................6 METHODS ..........................................................................................................................9 Surveys and Hand Capture.............................................................................................9 Trapping.......................................................................................................................11 -
Missouri Herpetological Association Newsletter #8 (1995)
Missouri Herpetological Association NNeewwsslleetttteerr Number 8 1995 Copyright © 1995 Missouri Herpetological Association MISSOURI HERPETOLOGICAL ASSOCIATION NEWSLETTER NO. 8 CONTENTS INTRODUCTION ..........…………............................................................................................................................. 2 ANNOUNCEMENT OF THE NINTH ANNUAL MHA MEETING ....…………................................................ 2 ABSTRACTS OF PAPER PRESENTED AT THE EIGHTH ANNUAL MHA MEETING ...........…………... 3 Life history, evolution, and adaptive radiation of hemidactyliine salamanders (Caudata: Plethodontidae: Hemidactyliini). T.J. Ryan. Pheromone communication in the Northern Water Snake, Nerodia sipedon. R.D. Aldridge and A.A. Reeves. Seasonal patterns of feedings and coelomic fat mass in the Diamondback Water Snake (Nerodia rhombifer) in Veracruz, México. R.D. Aldridge and K. Williams. A herpetofaunal survey of Ted Shanks Conservation Area. J. Graves and J.M. Jones. Herps are where the habitat is: Ted Shanks Conservation Area. J.M. Jones. Amphibian and reptile surveys of Fort Leonard Wood, Pulaski County, Missouri. S. Sanborn and J. Sternberg. Ecological interactions of vegetation and plethodontid salamanders for Missouri Ozark forests. L.A. Herbeck and D.R. Larsen. Herpetofaunal communities on the Missouri Ozark Forest Ecosystem Project (MOFEP): consistency among communities in pretreatment years? R. B. Renken. Herpetofaunal sampling using the LCTA Method at Lake Wappapello, Butler County, Missouri. R.L. Essner, Jr., A.J. Henderschott, and J.S. Scheibe. Habitat analysis of the Ozark Hellbender, Cryptobranchus alleganiensis bishopi, in Missouri. T.M. Fobes and R.F. Wilkinson, Jr. The occurrence, habitat use, and breeding status of an aquatic salamander, Amphiuma tridactylum, in southeastern Missouri. C.A. Cunningham and S. Trautwein. Effects of female mate choice on offspring fitness in the Gray Treefrog (Hyla versicolor). A.M. Welch and R.D. Semlitsch. -
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. -
The Venomous Snakes of Texas Health Service Region 6/5S
The Venomous Snakes of Texas Health Service Region 6/5S: A Reference to Snake Identification, Field Safety, Basic Safe Capture and Handling Methods and First Aid Measures for Reptile Envenomation Edward J. Wozniak DVM, PhD, William M. Niederhofer ACO & John Wisser MS. Texas A&M University Health Science Center, Institute for Biosciences and Technology, Program for Animal Resources, 2121 W Holcombe Blvd, Houston, TX 77030 (Wozniak) City Of Pearland Animal Control, 2002 Old Alvin Rd. Pearland, Texas 77581 (Niederhofer) 464 County Road 949 E Alvin, Texas 77511 (Wisser) Corresponding Author: Edward J. Wozniak DVM, PhD, Texas A&M University Health Science Center, Institute for Biosciences and Technology, Program for Animal Resources, 2121 W Holcombe Blvd, Houston, TX 77030 [email protected] ABSTRACT: Each year numerous emergency response personnel including animal control officers, police officers, wildlife rehabilitators, public health officers and others either respond to calls involving venomous snakes or are forced to venture into the haunts of these animals in the scope of their regular duties. North America is home to two distinct families of native venomous snakes: Viperidae (rattlesnakes, copperheads and cottonmouths) and Elapidae (coral snakes) and southeastern Texas has indigenous species representing both groups. While some of these snakes are easily identified, some are not and many rank amongst the most feared and misunderstood animals on earth. This article specifically addresses all of the native species of venomous snakes that inhabit Health Service Region 6/5s and is intended to serve as a reference to snake identification, field safety, basic safe capture and handling methods and the currently recommended first aide measures for reptile envenomation. -
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. -
Ventral Coloration and Body Condition Do Not Affect Territorial Behavior in Two Sceloporus Lizards
Ventral coloration and body condition do not affect territorial behavior in two Sceloporus lizards 1Marina Kelada, 1Courtney Moulton, 2Casey Nguyen, 3Griselda Robles Olague 1University of California, Riverside; 2University of California, Irvine; 3University of California, Santa Barbara Sceloporus lizards are known to be defensive of their territories, which provide shelter, food, water, and mates. They often exhibit territorial behavior through visual displays of aggression, specifically with pushups. Along with aggression, this display can also expose the blue coloration on their ventral side, serving as an intraspecific communication between lizards that reveals information about their dominance, sex, and species membership. In this study, we compared how blue coloration and body condition affected territorial behavior in two Sceloporus lizards: the well-studied western fence (Sceloporus occidentalis) and the understudied sagebrush (Sceloporus graciosus), two closely related lizards with overlapping ranges in the San Jacinto Mountains. We also addressed whether these species would exhibit character displacement in their ventral coloration as a result of their sympatry. ImageJ and Adobe Photoshop were used for photo analyses to quantify the proportion and intensity of blue on each lizard’s ventral side. Territoriality was measured through number of pushups displayed and distance traveled. We found that both ventral coloration and body condition had no effect on the territoriality of either species, suggesting that territorial behavior -
Maryland Envirothon: Wildlife Section
3/17/2021 Maryland Envirothon: Class Amphibia & Reptilia KERRY WIXTED WILDLIFE AND HERITAGE SERVICE March 2021 1 Amphibia Overview •>40 species in Maryland •Anura (frogs & toads) •Caudata (salamanders & newts) •Lay soft, jelly-like eggs (no shell) •Have larval state with gills •Breathe & drink through skin Gray treefrog by Kerry Wixted Note: This guide is an overview of select species found in Maryland. 2 Anura • ~20 species in Maryland • Frogs & toads • Short-bodied & tailless (as adults) • Typically lay eggs in water & hatch into aquatic larvae Green treefrog by Kerry Wixted Order: Anura 3 1 3/17/2021 Family Bufonidae (Toads) Photo by Kerry Wixted by Photo Kerry Photo by Judy Gallagher CC 2.0 CC by by Photo Gallagher Judy American Toad (Anaxyrus americanus ) Fowler's Toad (Anaxyrus fowleri) 2-3.5”; typically 1-2 spots/ wart; parotoid gland is 2-3”; typically 3+ spots/ wart; parotoid gland separated from the cranial crest or connected narrowly is in contact w/ the cranial crest; Call: a short, by a spur; enlarged warts on tibia; Call: an elongated trill brash and whiny call lasting 2-4 seconds or whir lasting 5-30 seconds and resembles a simultaneous whistle and hum Order: Anura; Family Bufonidae 4 Family Hylidae (Treefrogs) Spring Peeper Gray Treefrog & Cope’s Gray Treefrog (Pseudacris crucifer) (Hyla versicolor & Hyla chrysoscelis) 0.75 - 1.25”; Brown, tan, or yellowish with dark X-shaped 1.25 - 2” (Identical in appearance); Gray to white with mark on back; Dark bar between eye; Mask from nose darker streaking, resembling a tree knot; Cream square through eye and tympanum, often extending down side below each eye; Inner thigh yellow or orange; enlarged Call: Clear, shrill, high-pitched whistle or peep toe pads; Call (H.