COURTSHIP BEHAVIOR of the QUEEN SNAKE Regina

Total Page:16

File Type:pdf, Size:1020Kb

COURTSHIP BEHAVIOR of the QUEEN SNAKE Regina tion of the first 6 to 20 cm of the neck. It did PLASTIC BAGS IN THE COURTSHIP BEHAVIOR not involve any lateral sliding of the body but OF THE QUEEN SNAKE in other regards did appear to be similar to the INTESTINAL TRACTS writhe-bump seen by Gillingham in Elaphe Regina septemvittata (1979). Each bounce lasted 0.05 seconds and OF LEATHERBACK the bounce rate alternated between 60 to Studies of courtship and mating behavior MARINE TURTLES 70/min. up to 91 to 115/min. The slower rate of snakes have only recently been conducted involved higher dorsoventral movement (1 to carefully enough so that evolutionary aspects 2 cm off the female, Fig. 1). The faster rate While collecting skeletal material of Der- of this activity can be examined. In particular, occurred with oscillations in which the male mochelys coriacea at a site in coastal Peru Gillingham has used methods of frame by did not lose contact with the female's dorsum. where leatherback carcasses were discarded frame analysis of movie films to make com- After a variable period of this behavior, the by fishermen, I found evidence of plastic in parative studies of snake reproductive behav- males would begin the tail-search copulatory the intestinal tracts of these specimens to be ior (Gillingham, 1979). His work has been attempts. As the typical natricine caudal- common. Plastic bags and film were noted in primarily with species exhibiting what Davis cephalic waves were absent this suggests the 19 of 140 (13%) specimens examined in (1936) defined as "coluber" type courtship. vertical oscillations substitute for this repro- November 1980 near Pucusana, Depto. Lima, Several other authors have examined the ductive cue. Peru. The xeric climate of coastal Peru had reproductive patterns of the natricine snakes Male activity while mounted on the female's mummified many carcasses and slowed bio- (Blanchard and Blanchard, 1942; Pisani, 1976; trunk appears to show more evolutionary logical decomposition of tissues. Although Mushinsky, 1979), but species differences variability than do other stages of courtship. all specimens examined had been butchered have not been discussed. Regina is known to Gillingham (1979), for example, compared some considerable time before discovery be a quite distinct genus of natricine snake, the variation in caudal-cephalic waves and (perhaps more than 14 months earlier), the particularly in several behavioral characteris- writhe-bumps in Elaphe occurring during this intestines had been left in the carapaces and tics, i.e. feeding behavior. Its reproductive period. Regina septemvittata's different tac- had dried in situ. No attempt was made to behavior might therefore also exhibit varia- tile behavior also supports this idea. It, there- open or examine the entire digestive tract due tion from the typical pattern. This report is the fore, seems likely that these species differen- to the dried, rotted, and often incomplete first dealing with courtship activity of any ces in tactile activity of males while aligned nature of the viscera. Consequently, all cases member of Regina and examines the mating on the female have evolutionary implications. where plastic was noted involved sizable behavior of the Queen snake, Regina septem- The most logical explanation is that they con- pieces of plastic which protruded or were vittata. vey species specific identification designed exposed from the intestine. In all cases the Male and female Regina septemvittata were to bring about female passivity. Examination plastic was noted to be within the lumen of collected in the springs of 1978 and 1979 from of the tactile-alignment behavior of both the digestive tract and in a twisted, elongate southwestern Ohio. Within a few days of cap- closely related and evolutionarily distinct form suggesting peristalic transport. Because ture, these snakes were placed together in a species should give more insight into this of the limiting conditions under which obser- large aquarium (1.5m x 1/2m) containing a possibility. vations were made, the actual occurrence of gravel substrate. Courtship behavior of four plastic in Dermochelys is probably much males was observed and filmed with a super 8 ACKNOWLEDGMENTS higher than recorded. movie camera. The films were then analyzed Hays and Brown (1981) found plastic bags frame by frame for certain behavioral com- I thank George Pisani and James Gilling- in 9 of 39 (23%) specimens of Chelonia mydas ponents of courtship. ham for their comments on this manuscript. captured near Pisco, Depto. Ica, Peru. Coast- In most regards, male queen snakes showed al Peru is an area of low human population courtship behavior closely paralleling other LITERATURE CITED density. Consequently, the high incidence of natricines. The male approached and tongue plastic bags in the intestinal tracts of marine flicked the female repeatedly. The male Blanchard, F. N. and Blanchard, F. C. 1942. turtles is noteworthy. mounted the female and proceeded to move Mating of the garter snake, Thamnophis Brongersma (1969; 1972) recorded plastic forward until aligned on her dorsum. At this sirtalis sirtalis (Linnaeus). Papers, Michi- materials in the intestinal tracts of two leather- time the male queen snakes began a behavior gan Acad. Sci., Arts and Let., 27:215-234. backs from European waters. Carr (in Corne- different from other colubrids. They pro- Davis, D. D. 1936. Courtship and mating lius, 1975) attributed a mass mortality of Che- ceeded to "bounce" dorsoventrally on the behavior in snakes. Field Mus. Nat. Hist. lonia in Costa Rica to the ingestion of plastic female. This movement was a vertical oscilla- Zool. Series 20:257-290. bags. Pritchard (1971) mentioned that plastic Gillingham, J. C. 1979. Reproductive behav- is found in leatherback intestines. Carr and ior of the rat snakes of Eastern North Pritchard did not detail their observations. America, genus Elaphe. Copeia 1979(2): Mrosovsky (1981) recently reviewed data from 319-331. 16 leatherback turtles, 7 of which (44%) con- A Mushinsky, H. R. 1979. Mating behavior of the tained plastic. He also noted that 7 of 8 leather- common water snake, Nerodia sipedon backs studied in France by Duron and Duron sipedon (Reptilia, Serpentes, Colubridae) (1980) had swallowed plastic. The informa- in Eastern Pennsylvania. J. Herp. 13(1): tion on plastic bags in Chelonia and Der- 127-129. mochelys in Peru is important in confirming Pisani, G. R. 1976. Comments of the court- the incidence in a specified number of animals. ship and mating mechanics of Thamno- Frazier (1980) noted that plastics are indigest- phis (Reptilia, Serpentes, Colubridae). J. ible and they may impact the gut. The green B Herp. 10(2):139-142. turtles studied by Hays and Brown (in press) and the leatherbacks described herein were NEIL B. FORD butchered animals which presumably were Department of Biology captured alive. Therefore the plastics found had not yet caused death. Thus, the inci- The University of Texas at Tyler Tyler, Texas 75701 dence of turtles dying because of plastics is • unknown. The possibility of death or malnu- trition resulting from plastic bag impaction of C the gut should be carefully considered and investigated in dead or distressed animals Figure 1. The sequence of movements in a from other sources. Marine turtles actively single "bounce" of a male queen snake, Regina feed on jellyfish, and plastic bags floating in septemvittata, courting a female. water potentially resemble jellyfish in color, 72 Herp Review 13(3), 1982 form, and texture. Therefore, it is possible the box is constructed from a single 4 X 8 ft that plastics are consumed whenever en- TECHNIQUES sheet of one half inch plywood and miscel- countered by foraging marine turtles. Since laneous hardware. The box incorporates a plastic film products are used and disposed light bulb heat source, ventilation holes, an of worldwide, the potential for effecting A TIME-EFFICIENT, escape barrier, and a hinged access lid with marine organisms, including turtles, is great. LOW COST METHOD an inspection window. The individual com- ponents and specifications required to con- LITERATURE CITED FOR THE LABORATORY struct the basic box are provided in Fig. 1. REARING OF FROGS. Brongersma, L. D. 1969. Miscellaneous notes Figure 1. on turtles. II A-B Proc. Kon. Ned. Akad. INTRODUCTION Wet., Amsterdam 72(1):76-102. Rearing procedure. — Crickets (Acheta 1972. European Atlantic turtles. Zoo- There has long been a need for a reliable domestica) thrive under the appropriate logische Verhandelingen (121):1-318. method whereby laboratory populations of temperature and humidity conditions when Cornelius, S. E. 1975. Marine turtle mortali- anurans could be both maintained and per- provided with adequate water and food. ties along the Pacific coast of Costa Rica. petuated at modest cost and with minimal Commercial pelletized rabbit feeds provide Copeia 1975:186-187. time expenditure. The availability of reliable an excellent food source for crickets of all Duron, M. and P. Duron. 1980. Title unknown. methods for the raising and maintenance of ages. Alternatively, chicken mash can be Courrier de la Nature. 69:37-41. (Cited by anurans in a time-efficient operation and at used, but it is subject to mold. A 100 watt Mrosovsky 1981). modest cost is important to biologists in incandescent light bulb will maintain an inner Frazier, J. 1980. Marine turtles and problems many disciplines. However, small scale frog box temperature of about 32-40° C when the in coastal management. Pages 23495-2411 rearing operations are not common because box is placed in a room at 20-25° C. In a in: B. L. Edge (ed.) Proceedings of the of several fundamental problems. These cooler room, a bulb or higher wattage or mul- Second Symposium on Coastal and Ocean include: design inadequacies of many com- tiple bulbs can be used to bring the internal Management Vol. III. 17-20 November mercially available rearing tanks; lack of an box temperature to about 32-40° C.
Recommended publications
  • 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.
    [Show full text]
  • Veterans Park Herpetological Report Manning 2015
    To Whom It May Concern, The information in this document is the summary of a series of volunteer reptile and amphibian observations conducted in Hamilton Veteran’s Park in Mercer County, NJ. The document has been prepared for the Township of Hamilton. The results presented are from field observations and data collected in 2012, 2013, 2014, and 2015. The data from the first three years was taken informally during morning and evening walks with family. The data from 2015 was taken for a volunteer reptile and amphibian survey performed upon the request of the Township of Hamilton, Mercer County, NJ. This information is presented voluntarily for use in conservation endeavors. General Profile: Hamilton Veteran’s Park is a 350‐acre park managed by the Township of Hamilton in Mercer County, New Jersey. The park features a diversity of habitats within its boundaries, including a field which was the site of a former farm, a wetlands meadow, a smaller upland meadow, several patches of deciduous forest, a man‐made lake, temporary and permanent wetlands, an intermittent stream, and several permanent streams. The park is located on the physiographic province known as the inner coastal plain. Comments on General Fauna: The Veteran’s Park property provides a variety of habitats for native fauna to flourish. Healthy numbers of invertebrates have been observed during the survey. Checking under logs and other cover debris reveals a multitude of native decomposers, such as ants, earthworms, slugs, centipedes, harvestmen, and others. Ticks are occasionally seen in the fields, however most of those observed were dog ticks.
    [Show full text]
  • 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.
    [Show full text]
  • 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
    [Show full text]
  • Catesbeiana Is Published Twice a Year by the Virginia Herpetological Society
    BULLETIN INFORMATION Catesbeiana is published twice a year by the Virginia Herpetological Society. Membership is open to all individuals interested in the study of amphibians and reptiles and includes a subscription to Catesbeiana, two newsletters, and admission to all meetings. Annual dues for regular membership are $15.00 (see application form on last page for other membership categories). Payments received after September 1 of any given year will apply to membership for the following calendar year. Dues are payable to: Dr. Paul Sattler, VHS Secretary/Treasurer, Department of Biology, Liberty University, 1971 University Blvd., Lynchburg, VA 24502. HERPETOLOGICAL ARTWORK Herpetological artwork is welcomed for publication in Catesbeiana. If the artwork has been published elsewhere, we will need to obtain copyright before it can be used in an issue. We need drawings and encourage members to send us anything appropriate, especially their own work. EDITORIAL POLICY The principal function of Catesbeiana is to publish observations and original research about Virginia herpetology. Rarely will articles be reprinted in Catesbeiana after they have been published elsewhere. All correspondence relative to the suitability of manuscripts or other editorial matters should be directed to Dr. Steven M. Roble, Editor, Catesbeiana, Virginia Department of Conservation and Recreation, Division of Natural Heritage, 217 Governor Street, Richmond, VA 23219. Major Papers Manuscripts submitted for publication should be typewritten (double-spaced) on good quality SY2 by 11 inch paper, with adequate margins. Consult the style of articles in this issue for additional information, including the appropriate format for literature citations. The metric system should be used for reporting all types of measurement data.
    [Show full text]
  • 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.
    [Show full text]
  • 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.
    [Show full text]
  • REPTILIA: SQUAMATA: COLUBRIDAE Storeria
    900.1 REPTILIA: SQUAMATA: COLUBRIDAE Storeria Catalogue of American Amphibians and Reptiles. Ernst, C.H. 2012. Storeria . Storeria Baird and Girard American Brownsnakes Coluber : Linnaeus 1758:216. See Remarks . Storeria Baird and Girard 1853:135. Type -species, Tropidonotus dekayi Holbrook 1842:135 (officially so designated by the International Commission of Zoological Nomenclature [ICZN] 1962:145; see Remarks ). Ischnognathus Duméril 1853:468. Type -species, FIGURE 1. Storeria dekayi texana . Photograph by Suzanne L. Tropidonontus dekayi Holbrook 1842:53) Collins. Tropidoclonium : Cope 1865:190. Hemigenius Dugès 1888:182. Type -species, Hemi- genius variabilis Dugès 1888:182 (= Tropidoclo- nium storerioides Cope 1865:190). Natrix : Cope 1889:391. Tropidonotus : Duméril, Bocourt, and Mocquard 1893: 750. Thamnophis : Amaral 1929:21. Tropidoclonion : Dunn 1931:163. Storeia : Gray 2004:94. Ex errore . • CONTENT . Four species are recognized: Storeria FIGURE 2. Storeria hidalgoensis . Photograph by Michael S. dekayi, Storeria hidalgoensis, Storeria occipidomacu - Price. lata , and Storeria storerioides . See Remarks . • DEFINITION . Snakes of the genus Storeria are slender, cylindrical, relatively short (max. TL 40.6 cm), live -bearing, terrestrial worm and slug predators. Trunk vertebrae are small and elongate, with vault - ed neural arches containing well developed low spines that extend posteriorly beyond the arch. The somewhat pointed hypapophyses is also directed posteriorly. Condyles and cotyles are usually round, with lateral forimina present on the cotyles. The pre- zygapophyseal accessory processes are well devel - oped. A distinct haemal keel and subcentral ridges are present; and paired lateral processes occur on some caudal vertebrae. In the skull, the dentary bone is essentially not motile on the articular. FIGURE 3. Storeria occipitomaculata occipitomaculata .
    [Show full text]
  • Nerodia Sipedon), the Diamondback Watersnake
    A COMPARATIVE STUDY OF STRESS PHYSIOLOGY IN THE COMMON WATERSNAKE (NERODIA SIPEDON), THE DIAMONDBACK WATERSNAKE (NERODIA RHOMBIFER), AND THE QUEEN SNAKE (REGINA SEPTEMVITTATA). by Katharine Louise McCallie A Thesis Submitted in Partial Fulfillment of the Requirements for the Degree of Master of Science in Biology Middle Tennessee State University May 2018 Thesis Committee: Dr. Matthew Klukowski, Chair Dr. Vincent Cobb Dr. Ryan Otter ABSTRACT Vertebrates respond to stressors in part by increasing the secretion of glucocorticoids from the adrenal gland. Both intrinsic and extrinsic factors (e.g., age, sex, season) have been shown to influence glucocorticoid secretion within a species, but understanding of species differences in glucocorticoid secretory patterns is limited. In this study, I examined corticosterone, progesterone, and testosterone levels in the common watersnake (Nerodia sipedon), the diamondback watersnake (Nerodia rhombifer), and the queen snake (Regina septemvittata) at a capture baseline and in response to an acute 30 minute confinement stress. I also examined the same steroids in Nerodia sipedon subjected to three weeks of laboratory housing, a known chronic stressor. All three species exhibited elevated corticosterone in response to acute stress but baseline and post- stress levels varied among species. Overall, Nerodia sipedon and Nerodia rhombifer exhibited similar corticosterone and testosterone levels both at capture baseline and after 30 minutes of confinement stress. Regina septemvittata had substantially higher corticosterone levels than the two Nerodia species. Nerodia sipedon subjected to chronic stress showed no significant changes in corticosterone levels from the baseline to post-lab housing, suggesting downregulation of the hypothalamo-pituitary-adrenocortical axis and glucocorticoid production. ii TABLE OF CONTENTS Page LIST OF TABLES .
    [Show full text]
  • Snakes of New Jersey Brochure
    Introduction Throughout history, no other group of animals has undergone and sur- Snakes: Descriptions, Pictures and 4. Corn snake (Elaphe guttata guttata): vived such mass disdain. Today, in spite of the overwhelming common 24”-72”L. The corn snake is a ➣ Wash the bite with soap and water. Snakes have been around for over 100,000,000 years and despite the Range Maps state endangered species found odds, historically, 23 species of snakes existed in New Jersey. However, sense and the biological facts that attest to the snake’s value to our 1. Northern water snake (Nerodia sipedon sipedon): ➣ Immobilize the bitten area and keep it lower than your environment, a good portion of the general public still looks on the in the Pine Barrens of NJ. It heart. most herpetologists believe the non-venomous queen snake is now 22”-53”L. This is one of the most inhabits sandy, forested areas SNAKES OF extirpated (locally extinct) in New Jersey. 22 species of snakes can still snake as something to be feared, destroyed, or at best relegated to common snakes in NJ, inhabit- preferring pine-oak forest with be found in the most densely populated state in the country. Two of our glassed-in cages at zoos. ing freshwater streams, ponds, an understory of low brush. It ➣ lakes, swamps, marshes, and What not to do if bitten by a snake species are venomous, the timber rattlesnake and the northern All snakes can swim, but only the northern water snake and may also be found in hollow queen snake rely heavily on waterbodies.
    [Show full text]
  • Kansas Herpetological Society Newsletter No. 86 November 1991
    KANSAS HERPETOLOGICAL SOCIETY NEWSLETTER NO. 86 NOVEMBER 1991 ANNOUNCEMENTS SSAR REGIONAL SOCIETY LIAISON COMMIT­ Cincinnati Herpetological Society (GCHS) and send or­ TEE 1992 REGIONAL SOCIETIES CONFERENCE ders to: Greater Cincinnati Herpetological Society, c/o AND CALL FOR PAPERS Cincinnati Museum of Natural History, 1720 Gilbert Av­ enue, Cincinnati, Ohio, 45202. At the 1992 annual meeting of the Society for the Study of Amphibians and Reptiles at El Paso, Te:xas, the NEW GRANTS IN HERPETOLOGY Regional Society Liaison Committee will be sponsoring a one-day conference on "Federal and State Wildlife Laws The Chicago Herpetological Society (CHS) announces and Regulations and How They Affect Regional Herpeto­ the establishment of a new program to provide financial aid logical Societies". At this time, the committee is issuing a for herpetological research, education, and conservation. call for papers for anyone wishing to speak on this topic. Grants not to exceed $500 will be awarded in the following Topics addressed can be on any subject pertaining to the categories: Herpetology in lllinois, Graduate Student conference title and can be as formal or informal as the Research, Undergraduate (including high school) Research, speaker desires. Papers will be limited to twenty (20) Field Studies, Conservation, Captive Management, Hus­ minutes in length. Complete audiovisual services will be bandry, and Propagation, and a miscellaneous category for available. Those wishing to present a paper should send proposals that do not fit the foregoing categories. Appli­ title and a briefabstract no later than 15 December 1991 to: cants must be dues paying member of CHS. Recipients of Eric M Rundquist, Department of Herpetology, Sedgwick SSAR grants will be ineligible in the same calendar year.
    [Show full text]
  • Comparative Growth and Demographics of Two Sympatric Natricine Snakes
    COMPARATIVE GROWTH AND DEMOGRAPHICS OF TWO SYMPATRIC NATRICINE SNAKES Kent A. Bekker A Thesis Submitted to the Graduate College of Bowling Green State University in partial fulfillment of the requirements for the degree of MASTER OF SCIENCE December 2007 Committee: Dr. Daniel M. Pavuk, Advisor Dr. Richard B. King Dr. Jeffery G. Miner ii ABSTRACT Dr. Daniel M. Pavuk, Advisor The northern water snake, Nerodia sipedon and the queen snake, Regina septemvittata, are two species of the subfamily Natricinae that occur sympatrically throughout much of their ranges in Ohio. Regina septemvittata does not appear to be as abundant as it once was in much of its range, and published natural history information is lacking. Nerodia sipedon, however, has exhibited no decrease in abundance, and there is a relative abundance of published natural history information on this species. This study compares growth and population size for both species utilizing mark-recapture techniques and skeletochronology at the Sandusky Bay Fishing Access Site in Ottawa County, Ohio. The Sandusky Bay fishing access site supports populations of the following snake species: the northern water snake, Nerodia sipedon, the queen snake, Regina septemvittata, the eastern garter snake, Thamnophis sirtalis, Butler’s garter snake, Thamnophis butlerii, the eastern fox snake, Elaphe gloydi, and Dekay’s snake, Storeria dekayi. Population estimates for Nerodia sipedon result in densities similar to published values for nearby populations. Population estimates for Regina septemvittata displayed a decline over the course of the study, which was mirrored in the relative abundance of queen snake within the total sample for each year. Growth has an impact on snake conservation through delayed maturation, longer time spend at a size class experiencing a higher rate of mortality, and reduced reproductive advantage.
    [Show full text]