American Corn Snake Risk Assessment
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Resource Selection by an Ectothermic Predator in a Dynamic Thermal Landscape
Received: 2 May 2017 | Revised: 16 August 2017 | Accepted: 17 August 2017 DOI: 10.1002/ece3.3440 ORIGINAL RESEARCH Resource selection by an ectothermic predator in a dynamic thermal landscape Andrew D. George1 | Grant M. Connette2 | Frank R. Thompson III3 | John Faaborg1 1Division of Biological Sciences, University of Missouri, Columbia, MO, USA Abstract 2Smithsonian Conservation Biology Institute, Predicting the effects of global climate change on species interactions has remained Front Royal, VA, USA difficult because there is a spatiotemporal mismatch between regional climate models 3U.S.D.A. Forest Service Northern Research and microclimates experienced by organisms. We evaluated resource selection in a Station, Columbia, MO, USA predominant ectothermic predator using a modeling approach that permitted us to Correspondence assess the importance of habitat structure and local real- time air temperatures within Andrew D. George, Department of Biology, Pittsburg State University, Pittsburg, KS USA. the same modeling framework. We radio- tracked 53 western ratsnakes (Pantherophis Email: [email protected] obsoletus) from 2010 to 2013 in central Missouri, USA, at study sites where this spe- cies has previously been linked to prey population demographics. We used Bayesian discrete choice models within an information theoretic framework to evaluate the sea- sonal effects of fine- scale vegetation structure and thermal conditions on ratsnake resource selection. Ratsnake resource selection was influenced most by canopy cover, canopy cover heterogeneity, understory cover, and air temperature heterogeneity. Ratsnakes generally preferred habitats with greater canopy heterogeneity early in the active season, and greater temperature heterogeneity later in the season. This sea- sonal shift potentially reflects differences in resource requirements and thermoregula- tion behavior. -
Downloaded from Brill.Com10/06/2021 09:29:00AM Via Free Access 42 Luiselli Et Al
Contributions to Zoology, 74 (1/2) 41-49 (2005) Analysis of a herpetofaunal community from an altered marshy area in Sicily; with special remarks on habitat use (niche breadth and overlap), relative abundance of lizards and snakes, and the correlation between predator abundance and tail loss in lizards Luca Luiselli1, Francesco M. Angelici2, Massimiliano Di Vittorio3, Antonio Spinnato3, Edoardo Politano4 1 F.I.Z.V. (Ecology), via Olona 7, I-00198 Rome, Italy. E-mail: [email protected] 2 F.I.Z.V. (Mammalogy), via Cleonia 30, I-00152 Rome, Italy. 3 Via Jevolella 2, Termini Imprese (PA), Italy. 4 Centre of Environmental Studies ‘Demetra’, via Tomassoni 17, I-61032 Fano (PU), Italy Abstract relationships, thus rendering the examination of the relationships between predators and prey an extreme- A field survey was conducted in a highly degraded barren en- ly complicated task for the ecologist (e.g., see Con- vironment in Sicily in order to investigate herpetofaunal com- nell, 1975; May, 1976; Schoener, 1986). However, munity composition and structure, habitat use (niche breadth and there is considerable literature (both theoretical and overlap) and relative abundance of a snake predator and two spe- empirical) indicating that case studies of extremely cies of lizard prey. The site was chosen because it has a simple community structure and thus there is potentially less ecological simple communities, together with the use of appropri- complexity to cloud any patterns observed. We found an unexpect- ate minimal models, can help us to understand the edly high overlap in habitat use between the two closely related basis of complex patterns of ecological relationships lizards that might be explained either by a high competition for among species (Thom, 1975; Arditi and Ginzburg, space or through predator-mediated co-existence i.e. -
Xenosaurus Tzacualtipantecus. the Zacualtipán Knob-Scaled Lizard Is Endemic to the Sierra Madre Oriental of Eastern Mexico
Xenosaurus tzacualtipantecus. The Zacualtipán knob-scaled lizard is endemic to the Sierra Madre Oriental of eastern Mexico. This medium-large lizard (female holotype measures 188 mm in total length) is known only from the vicinity of the type locality in eastern Hidalgo, at an elevation of 1,900 m in pine-oak forest, and a nearby locality at 2,000 m in northern Veracruz (Woolrich- Piña and Smith 2012). Xenosaurus tzacualtipantecus is thought to belong to the northern clade of the genus, which also contains X. newmanorum and X. platyceps (Bhullar 2011). As with its congeners, X. tzacualtipantecus is an inhabitant of crevices in limestone rocks. This species consumes beetles and lepidopteran larvae and gives birth to living young. The habitat of this lizard in the vicinity of the type locality is being deforested, and people in nearby towns have created an open garbage dump in this area. We determined its EVS as 17, in the middle of the high vulnerability category (see text for explanation), and its status by the IUCN and SEMAR- NAT presently are undetermined. This newly described endemic species is one of nine known species in the monogeneric family Xenosauridae, which is endemic to northern Mesoamerica (Mexico from Tamaulipas to Chiapas and into the montane portions of Alta Verapaz, Guatemala). All but one of these nine species is endemic to Mexico. Photo by Christian Berriozabal-Islas. Amphib. Reptile Conserv. | http://redlist-ARC.org 01 June 2013 | Volume 7 | Number 1 | e61 Copyright: © 2013 Wilson et al. This is an open-access article distributed under the terms of the Creative Com- mons Attribution–NonCommercial–NoDerivs 3.0 Unported License, which permits unrestricted use for non-com- Amphibian & Reptile Conservation 7(1): 1–47. -
Caudal Distraction by Rat Snakes (Colubridae, Elaphe): a Novel Behavior Used When Capturing Mammalian Prey
Great Basin Naturalist Volume 59 Number 4 Article 8 10-15-1999 Caudal distraction by rat snakes (Colubridae, Elaphe): a novel behavior used when capturing mammalian prey Stephen J. Mullin University of Memphis, Memphis, Tennessee Follow this and additional works at: https://scholarsarchive.byu.edu/gbn Recommended Citation Mullin, Stephen J. (1999) "Caudal distraction by rat snakes (Colubridae, Elaphe): a novel behavior used when capturing mammalian prey," Great Basin Naturalist: Vol. 59 : No. 4 , Article 8. Available at: https://scholarsarchive.byu.edu/gbn/vol59/iss4/8 This Article is brought to you for free and open access by the Western North American Naturalist Publications at BYU ScholarsArchive. It has been accepted for inclusion in Great Basin Naturalist by an authorized editor of BYU ScholarsArchive. For more information, please contact [email protected], [email protected]. Great Ba....in Naturalist 59(4), ©1999, pp. 361....167 CAUDAL DISTRACTION BY RAT SNAKES (COLUBHIDAE, ELAPHE): A NOVEL BEHAVIOR USED WHEN CAPTURING MAMMALIAN PREY Stephen]. Mullin1 AJ3S11UCT.--el.mthtl movement in snakes trulY serve ei.ther a pl'Cdatory (e.g., caudal luring) or defensive (e.g., rattling, aposem,ttism) fUllction, I descliho n new behavioral pattern of tai.l movement in snakes. Gray rat snakl.'$ (Elaphe OhSO!etd spiloid.es) fi)raging on ~ma11 mmnmnls (Mus d01ne~·ticus) Inoved. their tails in un erratic, whiplike fashion uIter detecting prey in their vidnity. The thrashing movement in the horizontal plfme was audibly and visually obviolls, resulting in dis placement of leaf litter around the hlil. All subjects displayed the behavior, hilt not in all foraging episodes. -
Proceedings of the Indiana Academy Of
Serological Relationships among some Midwestern Snakes Sherman A. Minton Jr., Department of Microbilogy and Immunology Indiana University School of Medicine, Indianapolis, Indiana 46202 Abstract Using immunoelectrophoresis, serum samples from 24 species of midwestern snakes were reacted against antiserums raised against serums of Elaphe obsoleta, Natrix sipedon, and Agkistrodon piscivorus. On the basis of immunoelectrophoretic patterns, three clusters of species can be recognized. One consists of Natrix (3 sp.), Thamnophis (2 sp.), Regina septemvittata, Clonophis kirtlandi, Storeria dekayi and Virginia valeriae. A second consists of Elaphe (2 sp.), Lampropeltis (3 sp.) and Pituophis melanoleucus. The third consists of Agkistrodon (2sp.), Sistrurus catenatus, and Crotalus horridus. Five species {Coluber constrictor, Diadophis punctatus, Carphophis amoenus, Farancia abacura, and Heterodon platyrhinos) do not fit well into any of the above groups nor do they appear closely related to each other. Immunoelectrophoretic patterns do not indicate a markedly closer relationship between the Natrix and Elaphe groups of nonvenomous snakes than exists between these groups and the Agkistrodon group of pit vipers. Elaphe, Natrix and Agkistrodon all have species in east Asia, and the American groups presumably evolved from this stock. Other relationships and their zoogeographic implications are discussed. Introduction About 38 species of snakes occur in Indiana and adjoining states. Traditional taxonomy divides them into two families, the venomous pit vipers (Crotalinae, now generally considered a subfamily of the Viperidae) and the "typical nonvenomous snakes" of the family Colubridae. However, work during the past decade by investigators using both morphological and nonmorphological criteria has shown the Colubridae to be a highly heterogenous group (2,6,9,12,13). -
"Black Snakes": Identification and Ecology1
WEC214 "Black Snakes": Identification and Ecology1 Steve A. Johnson and Monica E. McGarrity2 Introduction Black-Colored Snakes in the Southeast The southeastern United States is home to a great diversity of snakes. There are about 45 species of Some snake species look quite similar and may snakes (only 6 of which are venomous) that may be be difficult for those inexperienced with snakes to found along the Atlantic and Gulf coastal states from confidently identify. Among these are several species Louisiana to North Carolina. These snakes live in a of southeastern snakes commonly called “black variety of upland and wetland habitats and play snakes” because of their primarily black coloration. important roles in the region's ecology. They are These include the Black Swampsnake, Black both predators and prey, and thus form important Ratsnake, Ring-necked Snake, Red-bellied links in natural food webs. Mudsnake, Black Pinesnake, Eastern Indigo Snake and the Southern Black Racer. The latter two — Regrettably, populations of many species of Eastern Indigo and Black Racer—are the species snakes are declining not only throughout the most often referred to as “black snakes”. southeastern United States but also worldwide. These declines are largely due to habitat loss and In addition to those listed above, individuals of degradation, high mortality on roads and pollution several species of water snakes, the Eastern associated with development, agriculture and other Hog-nosed Snake and the venomous Cottonmouth human activities. In addition, introduction of Moccasin may be black colored to a great extent, invasive species, disease, parasitism and even climate depending on the age of the individual and the habitat change may exert negative effects on snake in which it is found. -
Prey-Handling Behavior of Hatchling Elaphe Helena (Colubridae)
Herpetologica, 59(4), 2003, 469–474 Ó 2003 by The Herpetologists’ League, Inc. PREY-HANDLING BEHAVIOR OF HATCHLING ELAPHE HELENA (COLUBRIDAE) 1,2 RITA S. MEHTA Department of Biology, University of Texas, Tyler, TX 75719, USA ABSTRACT: The effects of prey size on prey-handling behavior for 60 ingestively naive hatchling Elaphe helena were studied in the laboratory. Hatchlings were randomly assigned to one of three diet categories in which prey (Mus musculus) varied by relative mass differences of 20–35%, 40–46%, or 50–59% of an individual snake’s own body mass. The effects of prey size on capture position, direction of ingestion, condition of prey at ingestion (dead/alive), feeding duration, and prey-handling tactic were observed and recorded for each feeding episode. Results indicated that prey size significantly affected the prey-handling behavior of hatchling E. helena. In the largest relative mass category, hatchlings captured prey by the anterior end more often than in the smaller two relative mass categories. Prey from the smallest relative mass category were simply seized whereas, in the medium and large categories, pinion and constriction behaviors were observed. Time to subdue and ingest the prey item increased with prey size categories. Key words: Colubridae; Effects of prey size; Elaphe helena; Prey-handling behavior THE SIZE, type, and activity level of various (i.e., press prey against the substrate with the prey are thought to influence the feeding anterior portion of the body) and constrict behaviors for many advanced snakes (de small active mice than nestling rats. Further- Queiroz, 1984; Moon, 2000). -
Elaphe Subocularis (Brown) Trans-Pecos Rat Snake
268.1 REPTILIA: SQUAMATA: SERPENTES: COLUBRIDAE ELAPHE SUBOCULARIS Catalogue of American Amphibians and Reptiles. of the Edwards Plateau south through Coahuila and Chihuahua, Mexico, including portions of eastern Durango and western Nue• WORTHINGTON,RICHARDD. 1980. Elaphe subocularis. vo Leon. Literature records include the following: New Mexico (Lewis, 1948, 1950; Dowling, 1957; Jameson, 1957; Gehlbach, 1959); Texas (Raun and Gehlbach, 11172and references there• Elaphe subocularis (Brown) in; Mather and Dixon, 1976; Tryon, 1976; Worthington, 1976); Trans-Pecos rat snake Chihuahua (Axtell and Webb, 1963); Coahuila (Smith, 1939; Schmidt and Owens, 1944); Durango (Webb, 1960); Nuevo Coluber subocularis Brown, 1901:492. Type-locality, "Davis Leon (Martin del Campo, 1953; Conant, 1965). Mountains, fifty miles southwest of Pecos, near the head of Toyah Creek." Holotype, Acad. Natur. Sci. Philadelphia 13733, adult male, collected by Mr. E. Mayenberg, 1901 (not • FOSSIL RECORD. Brattstrom (1964) reported Elaphe sub• examined by author). ocularis from several Pleistocene cave deposits on the western Elaphe subocularis: Stejneger and Barbour, 1917:84. Name val• flank of Pyramid Peak, Organ Mountains, Dona Ana County, New idated by Internat!. Comm. Zoo!. Nomenc!., 1965:182. Mexico .. Elaphe sclerotica: Smith, 1941:135. Substitute name for Coluber subocularis Brown, a secondary homonym of Bascanion sub• • PERTINENTLITERATURE. Important reviews are Dowling oculare Cope, 1866; name invalidated by Internat!. Comm. (1957), Wright and Wright (1957), -
Amphibians and Reptiles of the State of Coahuila, Mexico, with Comparison with Adjoining States
A peer-reviewed open-access journal ZooKeys 593: 117–137Amphibians (2016) and reptiles of the state of Coahuila, Mexico, with comparison... 117 doi: 10.3897/zookeys.593.8484 CHECKLIST http://zookeys.pensoft.net Launched to accelerate biodiversity research Amphibians and reptiles of the state of Coahuila, Mexico, with comparison with adjoining states Julio A. Lemos-Espinal1, Geoffrey R. Smith2 1 Laboratorio de Ecología-UBIPRO, FES Iztacala UNAM. Avenida los Barrios 1, Los Reyes Iztacala, Tlalnepantla, edo. de México, Mexico – 54090 2 Department of Biology, Denison University, Granville, OH, USA 43023 Corresponding author: Julio A. Lemos-Espinal ([email protected]) Academic editor: A. Herrel | Received 15 March 2016 | Accepted 25 April 2016 | Published 26 May 2016 http://zoobank.org/F70B9F37-0742-486F-9B87-F9E64F993E1E Citation: Lemos-Espinal JA, Smith GR (2016) Amphibians and reptiles of the state of Coahuila, Mexico, with comparison with adjoining statese. ZooKeys 593: 117–137. doi: 10.3897/zookeys.593.8484 Abstract We compiled a checklist of the amphibians and reptiles of the state of Coahuila, Mexico. The list com- prises 133 species (24 amphibians, 109 reptiles), representing 27 families (9 amphibians, 18 reptiles) and 65 genera (16 amphibians, 49 reptiles). Coahuila has a high richness of lizards in the genus Sceloporus. Coahuila has relatively few state endemics, but has several regional endemics. Overlap in the herpetofauna of Coahuila and bordering states is fairly extensive. Of the 132 species of native amphibians and reptiles, eight are listed as Vulnerable, six as Near Threatened, and six as Endangered in the IUCN Red List. In the SEMARNAT listing, 19 species are Subject to Special Protection, 26 are Threatened, and three are in Danger of Extinction. -
Checklist of Grundy County Missouri Amphibians and Reptiles for 2020
X = Recent collection (1987 or after) Checklist of Grundy County Missouri Amphibians and Reptiles for 2020 / = Historical collection (before 1987) Western Lesser Siren Mole Salamander Three-toed Amphiuma Four-toed Salamander Siren intermedia Ambystoma talpoideum Amphiuma tridactylum Hemidactylium scutatum Hellbender Small-mouthed Salamander Long-tailed Salamander Western Slimy Salamander Cryptobranchus alleganiensis Ambystoma texanum Eurycea longicauda Plethodon albagula Ringed Salamander Eastern Tiger Salamander Cave Salamander Ozark Zigzag Salamander Ambystoma annulatum / Ambystoma tigrinum Eurycea lucifuga Plethodon angusticlavius Spotted Salamander Central Newt Grotto Salamander Southern Red-backed Salamander Ambystoma maculatum Notophthalmus viridescens Eurycea spelaea Plethodon serratus Marbled Salamander Mudpuppy Oklahoma Salamander Ambystoma opacum Necturus maculosus Eurycea tynerensis Eastern Spadefoot Cope's Gray Treefrog Boreal Chorus Frog Southern Leopard Frog Scaphiopus holbrookii Hyla chrysoscelis Pseudacris maculata X Lithobates sphenocephalus Plains Spadefoot Green Treefrog Northern Crawfish Frog Wood Frog Spea bombifrons Hyla cinerea Lithobates areolatus Lithobates sylvaticus American Toad Gray Treefrog Plains Leopard Frog Eastern Narrow-mouthed Toad X Anaxyrus americanus / Hyla versicolor / Lithobates blairi Gastrophryne carolinensis Great Plains Toad Spring Peeper American Bullfrog Western Narrow-mouthed Toad Anaxyrus cognatus Pseudacris crucifer / Lithobates catesbeianus Gastrophryne olivacea Fowler's Toad Upland Chorus -
A Guide to Missouri's Snakes
A GUIDE TO MISSOURI’S SNAKES MISSOURI DEPARTMENT OF CONSERVATION A Guide to Missouri’s Snakes by Jeffrey T. Briggler, herpetologist, and Tom R. Johnson, retired herpetologist, Missouri Department of Conservation Photographs by Jeffrey T. Briggler, Richard Daniel, Tom R. Johnson, and Jim Rathert Edited by Larry Archer Design by Susan Ferber Front cover: Eastern milksnake. Photo by Jim Rathert. mdc.mo.gov Copyright © 2017 by the Conservation Commission of the State of Missouri Published by the Missouri Department of Conservation PO Box 180, Jefferson City, Missouri 65102–0180 Equal opportunity to participate in and benefit from programs of the Missouri Depart- ment of Conservation is available to all individuals without regard to their race, color, religion, national origin, sex, ancestry, age, sexual orientation, veteran status, or disability. Questions should be directed to the Department of Conser- vation, PO Box 180, Jefferson City, MO 65102, 573-751-4115 (voice) or 800-735-2966 (TTY), or to Chief, Public Civil Rights, Office of Civil Rights, U.S. Department of the Interior, 1849 C Street, NW, Washington, D.C. 20240. GET TO KNOW MISSOURI’S SNAKES Snakes have generated more fear and misunderstanding than any other group of animals. Psychologists have proven that a fear of snakes (called ophidiophobia) is acquired; we are not born with it. Once people learn some of the interesting facts about snakes and discover that most of them are harmless and beneficial, their aversion may diminish. With patience and understanding, almost anyone can overcome a dread of snakes and actually enjoy studying them. One thing is certain — even people with a well-developed fear of snakes are curious about them. -
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.