Effectiveness of Manual Palpation in the Northern Water Snake, Nerodia
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COTTONMOUTH Agkistrodon Piscivorus
COTTONMOUTH Agkistrodon piscivorus Agkistrodon is derived from ankistron and odon which in Greek mean “fishhook” and “tooth or teeth;” referring to the curved fangs of this species. Piscivorus is derived from piscis and voro which in Latin mean “fish” and “to eat”. Another common name for cottonmouth is water moccasin. The Cottonmouth is venomous. While its bite is rarely fatal, tissue damage is likely to occur and can be severe if not treated promptly. IDENTIFICATION Appearance: The cottonmouth is a stout- bodied venomous snake that reaches lengths of 30 to 42 inches as adults. Most adults are uniformly dark brown, olive, or black, tending to lose the cross banded patterning with age. Some individuals may have a dark cheek stripe (upper right image). The cottonmouth has the diagnostic features of the pit-viper family such as a wedge-shaped head, sensory pits between the eyes and nostrils, and vertical “cat-like” pupils. Juveniles are lighter and more boldly patterned with a yellow coloration toward the tip of the tail (lower right image). Dorsal scales are weakly keeled, and the subcaudal scales form only one row. Cottonmouths also have a single anal Mike Redmer plate. Subspecies: There are three subspecies of the cottonmouth. The Western Cottonmouth (A. p. leucostoma) is the only subspecies found in the Midwest. The term leucostoma refers to the white interior of mouth. Confusing Species: The non-venomous watersnakes (Nerodia) are commonly confused with Cottonmouths across their range, simply because they are snakes in water. Thus it is important to note that Cottonmouths are only found in southernmost Midwest. -
Northern Watersnake Selection of Fish Prey in Western Kentucky
Northern Watersnake Diet . Perkins and Eason Northern Watersnake Selection of Fish Prey in Western Kentucky Micah W. Perkins 1, Department of Biology, University of Louisville, 139 Life Sciences Building, Louisville, KY 40292 Perri K. Eason, Department of Biology, University of Louisville, 139 Life Sciences Building, Louisville, KY 40292 Abstract: Watersnakes serve a variety of important roles in aquatic ecosystems with many species being of conservation interest. The northern water- snake (Nerodia sipedon) has some populations of concern, but is found in a wide variety of aquatic habitats throughout North America. Although pre- vious studies have examined the diet of this typically piscivorous species, research has not addressed whether the northern watersnake is preferentially selecting particular fish as prey. In this study, we sampled snake stomach contents and used Chesson’s alpha selection index α( i) to investigate whether northern watersnakes are eating fish families in proportion to their availability or are preferentially selecting or avoiding specific fish families. At the Sloughs Wildlife Management Area in western Kentucky, the northern watersnake fed on fish from six families in 2013 (n = 15) and 2014 (n = 36). Five of those fish families were eaten in proportion to their availability but avoided pirate perch (Aphredoderus sayanus), the lone member of the family Aphredoderidae. This is the first study testing prey preferences in the northern watersnake. Key words: northern watersnake, Nerodia sipedon, diet selection, fish family, pirate perch Journal of the Southeastern Association of Fish and Wildlife Agencies 5:144–149 Many watersnakes are of conservation concern and can poten- igan shifted from a heavily amphibian-based diet to feeding only on tially be used as indicators to understand harmful human impacts fishes (Meyer 1992, Carbone 1993). -
Expanded Description of a Chinese Endemic Snake Opisthotropis Cheni (Serpentes: Colubridae: Natricinae)
Asian Herpetological Research 2010, 1(1): 57-60 DOI: 10.3724/SP.J.1245.2010.00057 Expanded Description of a Chinese Endemic Snake Opisthotropis cheni (Serpentes: Colubridae: Natricinae) LI Cao1, LIU Qin1 and GUO Peng 1, 2* 1 Department of Life Sciences and Food Engineering, Yibin University, Yibin 644000, Sichuan, China 2 Chendgu Institute of Biology, Chinese Academy of Sciences, Chengdu 610041, Sichuan, China Abstract Based on seven newly-collected specimens, we provide an expanded description for the rare Chinese snake Opisthotropis cheni. The new specimens are consistent with the type series in scale counts and body dimensions. How- ever, two individuals lack yellow cross-bands that are apparent in the type specimens. A key to the ten Chinese species of Opisthotropis is provided. Keywords snake, Opisthotropis cheni, morphology, China 1. Introduction 070140, 071041, 071046-071050) (Table 1), collected from the Nanling National Nature Reserve in Ruyuan The genus Opisthotropis Gǘnther (1872) is comprised of County, Guangdong Province, China (Figure 1), were 17 currently recognized species, and is widely distributed morphologically examined in this work. The specimens in eastern, southern, and southeastern Asia (Uetz, 2010). were preserved in 8% formalin for initial fixation, and Members of this genus are all small aquatic snakes, later transferred to 75% ethanol. All specimens were de- mainly inhabiting rapidly flowing streams or small rivers. posited at Yibin University (YBU), Sichuan Province, Ten species of Opisthotropis occur in China (Zhao, China. 2006). Snout-vent length (SVL) and tail length (TL) were Zhao (1999) described Opisthotropis cheni based on measured using a meter ruler to the nearest millimeter, four specimens collected from Mt. -
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. -
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. -
Fauna of Australia 2A
FAUNA of AUSTRALIA 26. BIOGEOGRAPHY AND PHYLOGENY OF THE SQUAMATA Mark N. Hutchinson & Stephen C. Donnellan 26. BIOGEOGRAPHY AND PHYLOGENY OF THE SQUAMATA This review summarises the current hypotheses of the origin, antiquity and history of the order Squamata, the dominant living reptile group which comprises the lizards, snakes and worm-lizards. The primary concern here is with the broad relationships and origins of the major taxa rather than with local distributional or phylogenetic patterns within Australia. In our review of the phylogenetic hypotheses, where possible we refer principally to data sets that have been analysed by cladistic methods. Analyses based on anatomical morphological data sets are integrated with the results of karyotypic and biochemical data sets. A persistent theme of this chapter is that for most families there are few cladistically analysed morphological data, and karyotypic or biochemical data sets are limited or unavailable. Biogeographic study, especially historical biogeography, cannot proceed unless both phylogenetic data are available for the taxa and geological data are available for the physical environment. Again, the reader will find that geological data are very uncertain regarding the degree and timing of the isolation of the Australian continent from Asia and Antarctica. In most cases, therefore, conclusions should be regarded very cautiously. The number of squamate families in Australia is low. Five of approximately fifteen lizard families and five or six of eleven snake families occur in the region; amphisbaenians are absent. Opinions vary concerning the actual number of families recognised in the Australian fauna, depending on whether the Pygopodidae are regarded as distinct from the Gekkonidae, and whether sea snakes, Hydrophiidae and Laticaudidae, are recognised as separate from the Elapidae. -
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. -
Nerodia Taxispilota)
ECOLOGY AND LIFE HISTORY OF THE BROWN WATER SNAKE (NERODIA TAXISPILOTA) by MARK S. MILLS (Under the direction of Dr. J. Whitfield Gibbons) ABSTRACT Population parameters, habitat, diet, reproductive traits, and other natural history characteristics of the brown water snake, Nerodia taxispilota, from the Savannah River Site, South Carolina, USA, were determined or estimated using mark-recapture data collected over an 8-yr period (1991-1998). Population size estimates for a 10-km section of the Savannah River ranged from 2782 - 3956 (approximately 0.14 - 0.20 snakes/m of shoreline). Growth was similar in juveniles of both sexes, but adult females grew significantly faster than adult males. Life history traits for this population include: 1) relatively high adult survivorship, 2) estimated ages at maturity of approximately 5-6 years for females and 3 years for males, 3) relatively long-lived (6+yr) individuals, 4) high fecundity (mean litter size =18.2), and 5) annual reproduction by females larger than 115 cm SVL. Litter size was positively correlated with female length and mass. No apparent trade-off exists between litter size and offspring size. Brown water snakes were not randomly distributed and were significantly associated with the steep-banked outer bends of the river and availability of potential perch sites. River sections with the highest number of captures were clustered within 200 m of backwater areas. Most (70%) of 164 recaptured N. taxispilota were <250 m from their previous capture site; however, three moved >1 km. Only large (>80 cm snout-vent length) individuals (n = 8) crossed the river (approximately 100 m). -
COPPERBELLY WATER SNAKE Nerodia Erythrogaster Neglecta Identification, Status, Ecology, and Conservation in the Midwest
COPPERBELLY WATER SNAKE Nerodia erythrogaster neglecta Identification, Status, Ecology, and Conservation in the Midwest IDENTIFICATION General Appearance Adult copperbellies are uniformly dark brown to black on their dorsal surface, and have an orange, red, or perhaps even yellowish belly, the color of which extends up onto the chin. The dark dorsal may appear as ‘finger- like’ projections of color ‘bleeding’ down from the lateral scales. In some cases, Copperbellies clean up pretty well. Their dark dorsal coloration the dark coloration can contrasts with a yellow or orange belly and throat color. Photo heavily invade the belly by M. Myers. color as dark bands. However, the dark coloration never occurs in half-moon crescents. Copperbellies can be quite large, with adults growing to lengths of 40-50 inches. Juveniles, in contrast to the adults, have a strongly blotched and banded pattern similar to that of other young water snakes. Comparisons Amongst Subspecies The copperbelly is the Midwestern representative subspecies of the “plainbelly” water snake, Nerodia erythrogaster, which ranges throughout the central and southeastern United States. The most similar plainbelly subspecies is the Redbelly Water Snake ( N. e. erythrogaster). However, this is an East Coast form. The Yellowbelly Water Snake (N. e. flavigaster) is the subspecies that is closest to the copperbelly geographically. Yellowbellies and copperbellies co-occur in areas of southern Illinois and western Kentucky, and some intergradation is apparent. As suggested by the name, the belly color of the yellowbelly is more typically yellow rather than orange. The dorsal color of the yellowbelly is more of a light brownish than the dark brown or “black” of the copperbelly. -
Garter Snake Population Dynamics from a 16-Year Study: Considerations for Ecological Monitoring
Ecological Applications, 15(1), 2005, pp. 294±303 q 2005 by the Ecological Society of America GARTER SNAKE POPULATION DYNAMICS FROM A 16-YEAR STUDY: CONSIDERATIONS FOR ECOLOGICAL MONITORING AMY J. LIND,1 HARTWELL H. WELSH,JR., AND DAVID A. TALLMON2 USDA Forest Service, Paci®c Southwest Research Station, Redwood Sciences Laboratory, 1700 Bayview Drive, Arcata, California 95521 USA Abstract. Snakes have recently been proposed as model organisms for addressing both evolutionary and ecological questions. Because of their middle position in many food webs they may be useful indicators of trophic complexity and dynamics. However, reliable data on snake populations are rare due to the challenges of sampling these patchily distributed, cryptic, and often nocturnal species and also due to their underrepresentation in the eco- logical literature. Studying a diurnally active stream-associated population of garter snakes has allowed us to avoid some of these problems so that we could focus on issues of sampling design and its in¯uence on resulting demographic models and estimates. From 1986 to 2001, we gathered data on a population of the Paci®c coast aquatic garter snake (Thamnophis atratus) in northwestern California by conducting 3±5 surveys of the population annually. We derived estimates for sex-speci®c survival rates and time-dependent capture probabilities using population analysis software and examined the relationship between our calculated capture probabilities and variability in sampling effort. We also developed population size and density estimates and compared these estimates to simple count data (often used for wildlife population monitoring). Over the 16-yr period of our study, we marked 1730 snakes and had annual recapture rates ranging from 13% to 32%. -
161-168, 1992 an Identification Key to the Reptiles of The
RIc. zool. SU1V. Indio, 91 (2) : 161-168, 1992 AN IDENTIFICATION KEY TO THE REPTILES OF THE KALAKAD WILDLIFE SANCTUARY, TAMI~ NADU, INDIA T. S. N. MURTHY Zoological Survey of India Madras 600 028 INTRODUCTION Reptiles, despite the fact that they are predominant, are neglected in the past by the resource managers and the administrators in-charge of the conservation areas such as the sanctuaries and the biosphere reserves in India. One reason is that the information on the herpetology of the protected areas is scanty and no keys covering the reptiles are published. Another is that the definitive volumes on Indian reptiles by Malcolm Smith (1931, 1935, 1943) were written with the specialist in mind. The present key, based on recent material taken from stations located in the heart of the KWLS by the scientists of the Southern Regional Station (SRS) of the Zoological Survey of India (ZSI) and the findings of other workers, is expected to fulfill an urgent need. The majority of reptiles inhabiting the sanctuary are included in the key, but further study is needed to determine the entire herpetofauna of KWLS. It is felt, therefore, that this work will enable the biologists/naturalists interested in the herpetology of the K WLS to identify the reptiles of the area and thereby facilitate future recognition of species not previously recorded from the sanctuary. PHYSIOGRAPHY OF THE KALAKAD SANCTUARY The Kalakad Wildlife Sanctuary is located in Nanguneri Taluq, Tirunelveli District of Tamil Nadu (See Maps 1-2) and lies between latitudes 8°2S'N and g03S'N and longitudes between 77°2S'E and 77°3S'E. -
Northern Watersnake, Nerodia Sipedon
Invasive Species Fact Sheet Northern watersnake, Nerodia sipedon General Description Northern watersnakes are thick-bodied, aquatic snakes that can reach up to 4 ½ feet in length. There are four subspecies of northern watersnake: Lake Erie, midland, common, and Carolina. All subspecies have black, dark brown, or reddish crossbands on the front section of the body that break up into rows of blotches from the middle to the end of the body. Their bellies can be white, yellow, or orange, and commonly have dark half-mooned shaped spots. Body color of northern watersnakes can vary from reddish to brown to gray to black. Older northern watersnakes often appear to be almost entirely dark Juvenile northern watersnake Photo by Todd Pierson brown or black in color. Northern watersnakes are not venomous, but when threatened will strike repeatedly and emit a foul-smelling musk mixed with feces. Current Distribution In California, northern watersnakes have been established and reproducing in Kaseberg Creek in the City of Roseville, Placer County since 2007. In 2014, they were discovered in another separate location within Roseville. Northern watersnakes do not naturally occur west of the Rocky Mountains. They are native to the eastern United States from Mississippi and Alabama, through the Carolinas to Maine in the east, and through Kansas and Nebraska to the Great Lakes region in the north. Habitat Preference Northern watersnakes live in freshwater habitats such as ditches, ponds, lakes, wetlands, and slow-moving streams and rivers. They are commonly found basking in the sun in shallow water areas on natural Adult northern watersnake; Placer County and manmade structures such as overhanging branches, logs, docks, Photo by Gary Nafis, California Herps and piers.