Great Basin Gophersnake,Pituophis Catenifer Deserticola
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Birds, Reptiles, Amphibians, Vascular Plants, and Habitat in the Gila River Riparian Zone in Southwestern New Mexico
Birds, Reptiles, Amphibians, Vascular Plants, and Habitat in the Gila River Riparian Zone in Southwestern New Mexico Kansas Biological Survey Report #151 Kelly Kindscher, Randy Jennings, William Norris, and Roland Shook September 8, 2008 Birds, Reptiles, Amphibians, Vascular Plants, and Habitat in the Gila River Riparian Zone in Southwestern New Mexico Cover Photo: The Gila River in New Mexico. Photo by Kelly Kindscher, September 2006. Kelly Kindscher, Associate Scientist, Kansas Biological Survey, University of Kansas, 2101 Constant Avenue, Lawrence, KS 66047, Email: [email protected] Randy Jennings, Professor, Department of Natural Sciences, Western New Mexico University, PO Box 680, 1000 W. College Ave., Silver City, NM 88062, Email: [email protected] William Norris, Associate Professor, Department of Natural Sciences, Western New Mexico University, PO Box 680, 1000 W. College Ave., Silver City, NM 88062, Email: [email protected] Roland Shook, Emeritus Professor, Biology, Department of Natural Sciences, Western New Mexico University, PO Box 680, 1000 W. College Ave., Silver City, NM 88062, Email: [email protected] Citation: Kindscher, K., R. Jennings, W. Norris, and R. Shook. Birds, Reptiles, Amphibians, Vascular Plants, and Habitat in the Gila River Riparian Zone in Southwestern New Mexico. Open-File Report No. 151. Kansas Biological Survey, Lawrence, KS. ii + 42 pp. Abstract During 2006 and 2007 our research crews collected data on plants, vegetation, birds, reptiles, and amphibians at 49 sites along the Gila River in southwest New Mexico from upstream of the Gila Cliff Dwellings on the Middle and West Forks of the Gila to sites below the town of Red Rock, New Mexico. -
Pituophis Catenifer
COSEWIC Assessment and Status Report on the Gophersnake Pituophis catenifer Pacific Northwestern Gophersnake – P.c. catenifer Great Basin Gophersnake – P.C. deserticola Bullsnake – P.C. sayi in Canada EXTIRPATED - Pacific Northwestern Gophersnake – P.c. catenifer THREATENED - Great Basin Gophersnake – P.c. deserticola DATA DEFICIENT - Bullsnake – P.c. sayi 2002 COSEWIC COSEPAC COMMITTEE ON THE STATUS OF COMITÉ SUR LA SITUATION DES ENDANGERED WILDLIFE IN ESPÈCES EN PÉRIL CANADA AU CANADA COSEWIC status reports are working documents used in assigning the status of wildlife species suspected of being at risk. This report may be cited as follows: Please note: Persons wishing to cite data in the report should refer to the report (and cite the author(s)); persons wishing to cite the COSEWIC status will refer to the assessment (and cite COSEWIC). A production note will be provided if additional information on the status report history is required. COSEWIC 2002. COSEWIC assessment and status report on the Gophersnake Pituophis catenifer in Canada. Committee on the Status of Endangered Wildlife in Canada. Ottawa. vii + 33 pp. Waye, H., and C. Shewchuk. 2002. COSEWIC status report on the Gophersnake Pituophis catenifer in Canada in COSEWIC assessment and status report on the Gophersnake Pituophis catenifer in Canada. Committee on the Status of Endangered Wildlife in Canada. Ottawa. 1-33 pp. For additional copies contact: COSEWIC Secretariat c/o Canadian Wildlife Service Environment Canada Ottawa, ON K1A 0H3 Tel.: (819) 997-4991 / (819) 953-3215 Fax: (819) 994-3684 E-mail: COSEWIC/[email protected] http://www.cosewic.gc.ca Ếgalement disponible en français sous le titre Évaluation et Rapport du COSEPAC sur la situation de la couleuvre à nez mince (Pituophis catenifer) au Canada Cover illustration: Gophersnake — Illustration by Sarah Ingwersen, Aurora, Ontario. -
Bull Snake Class: Reptilia
Pituophis catenifer sayi Bull Snake Class: Reptilia. Order: Squamata. Family: Colubridae. Other names: Gopher Snake, Pine Snake Physical Description: Bull snakes are usually yellow in color, with brown, black or reddish colored blotching or saddle spots on the sides of the snake. There are dark spots placed between the blotches or saddle spots. Below this is a further row of smaller dark spots. The belly is light brown. Many variations in color have been found, including albinos and white variations. This snake has a small head and a large nose shield, which it uses to dig. They often exceed 6 feet in length, with specimens of up to 100 inches being recorded. Males are generally larger then females. The bull snake is a member of the family of harmless snakes, or Colubridae. This is the largest order of snakes, representing two-thirds of all known snake species. Members of this family are found on all continents except Antarctica, widespread from the Arctic Circle to the southern tips of South America and Africa. All but a handful of species are harmless snakes, not having venom or the ability to deliver toxic saliva through fangs. Most harmless snakes subdue their prey through constriction, striking and seizing small rodents, birds or amphibians and quickly wrapping their body around the prey causing suffocation. While other small species such as the common garter snake lack powers to constrict and feed on only small prey it can overpower. Diet in the Wild: Bull snakes eat small mammals, such as mice, rats, large bugs as well as ground nesting birds, lizards and the young of other snakes. -
Identifying Amphibians and Reptiles in Zoos and Aquariums ZOO VIEW
290 ZOO VIEW Herpetological Review, 2015, 46(2), 290–294. © 2015 by Society for the Study of Amphibians and Reptiles Identifying Amphibians and Reptiles in Zoos and Aquariums PLUS ҫa ChanGe, PluS C’eST la même ChoSe [The more ThinGS ChanGe, Snakes and their allies were traditionally placed in the genus THE MORE THEY STAY THE SAME] Elaphe but were recently referred to Pantherophis based on their —JEAN-BAPTISTE ALPHONSE KARR, 1849 close relationship to other lampropeltine colubrids of the New World (Burbrink and Lawson 2007). Different combinations are Reptiles and amphibians are relatively unique in the sense used by different authors and my colleagues are struggling with of constantly changing taxonomies. That phenomenon simply is these differences; in other words, which names should they use? not a big operative problem for bird and mammal zoo person- Some biologists believe that there is a rule that the most recent nel. To gain a sense of why this is happening, refer to Frost and taxonomic paper should be the one used but there is no such Hillis (1990). There is confusion caused by changes in both stan- established convention in the Code (The International Code of dard and scientific names in herpetology. The general principle Zoological Nomenclature). Recently, a convincing description of in a zoo is that one wants to be talking about the same species the dangers of taxonomic vandalism leading to potential desta- when putting live animals together for breeding or exhibit or bilization has appeared in the literature (Kaiser et al. 2013) and analyzing records for genealogy or research. -
Okanagan Range Ecoregion
Selecting Plants for Pollinators A Guide for Gardeners, Farmers, and Land Managers In the Okanagan Range Ecoregion Keremeos and Hedley Table of CONTENTS Why Support Pollinators? 4 Getting Started 5 Okanagan range 6 Meet the Pollinators 8 Plant Traits 10 Developing Plantings 12 Farms 13 Public Lands 14 Home Landscapes 15 Plants That Attract Pollinators 16 Habitat hints 20 Habitat and Nesting requirements 21 S.H.A.R.E. 22 Checklist 22 This is one of several guides for different regions of North America. Resources and Feedback 23 We welcome your feedback to assist us in making the future guides useful. Please contact us at [email protected] 2 Selecting Plants for Pollinators Selecting Plants for Pollinators A Guide for Gardeners, Farmers, and Land Managers In the Okanagan Range Ecoregion Keremeos and Hedley A NAPPC and Pollinator Partnership Canada™ Publication Okanagan Range 3 Why support pollinators? IN THEIR 1996 BOOK, THE FORGOTTEN POLLINATORS, Buchmann and Nabhan estimated that animal pollinators are needed for the reproduction “Flowering plants of 90% of fl owering plants and one third of human food crops. Each of us depends on these industrious pollinators in a practical way to provide us with the wide range of foods we eat. In addition, pollinators are part of the across wild, intricate web that supports the biological diversity in natural ecosystems that helps sustain our quality of life. farmed and even Abundant and healthy populations of pollinators can improve fruit set and quality, and increase fruit size. In farming situations this increases production per hectare. In the wild, biodiversity increases and wildlife urban landscapes food sources increase. -
Minfile Nts 082Ese - Grand Forks
MINFILE NTS 082ESE - GRAND FORKS Original release date: 1997 Researched and compiled by: B.N. Church and L.D. Jones The Grand Forks map area, located in south-central British Columbia, contains 261 documented mineral occurrences, including 108 past producers. The map area includes the historically important Greenwood mining camp, which continues to attract exploration interest and activity. Physiographic domains include the Okanagan Highland over most of the map area, and the Selkirk Mountains to the east of Lower Arrow Lake. The map area lies in the Omineca tectonic belt, which formed in Early to Middle Jurassic time as a result of the accretion of Paleozoic and Mesozoic oceanic and arc rocks of the Slide Mountain and Quesnel terranes. These terranes were delaminated from the oceanic lithosphere and stacked against the continental margin of the North America craton. The resulting calc-alkaline plutonism created a large number of Middle Jurassic intrusions of intermediate composition. These intrude the accreted terranes and the Proterozoic pericratonic Monashee Complex. Overprinting by Cretaceous Laramide and post-Laramide Tertiary transtensional structures has complicated the geology. Paleozoic age, unconformable bedded assemblages include the Knob Hill, Attwood and Anarchist groups. Knob Hill Group is Permo-Carboniferous, and possibly as old as Devonian, and consists of massive and banded MINFILE NTS 082ESE - Grand Forks metacherts and lesser amounts of quartz chlorite schist, amphibolitic schists and gneisses, and limestone bands. The rocks have been affected by deformation and metamorphism causing recrystallization and the development of foliation, quartz sweats parallel to foliation and much deformation of individual beds. The Attwood Group is Permian and consists of black argillite, sharpstone conglomerate, greywacke, limestone lenses and metavolcanic units. -
Adult Red-Headed Woodpecker Interac- Tion with Bullsnake After Arboreal Nest Depredation
University of Nebraska - Lincoln DigitalCommons@University of Nebraska - Lincoln The Prairie Naturalist Great Plains Natural Science Society 6-2017 ADULT RED-HEADED WOODPECKER INTERAC- TION WITH BULLSNAKE AFTER ARBOREAL NEST DEPREDATION Brittney J. Yohannes James L. Howitz Follow this and additional works at: https://digitalcommons.unl.edu/tpn Part of the Biodiversity Commons, Botany Commons, Ecology and Evolutionary Biology Commons, Natural Resources and Conservation Commons, Systems Biology Commons, and the Weed Science Commons This Article is brought to you for free and open access by the Great Plains Natural Science Society at DigitalCommons@University of Nebraska - Lincoln. It has been accepted for inclusion in The Prairie Naturalist by an authorized administrator of DigitalCommons@University of Nebraska - Lincoln. The Prairie Naturalist 49:23–25; 2017 ADULT RED-HEADED WOODPECKER INTERAC- 100 m away from the first observation. To our knowledge, TION WITH BULLSNAKE AFTER ARBOREAL this is the first documented observation of red-headed wood- NEST DEPREDATION—Nest success rates often are pecker nest depredation by any subspecies of gopher snake, higher among cavity nesting birds than those that nest in and the first documented case of an adult red-headed wood- open cups or on the ground (Martin and Li 1992, Wesołowski pecker actively defending its nest against snake predation. and Tomiłojć 2005). Among cavity nesting birds, woodpeck- On 10 June 2015, we were monitoring red-headed wood- ers have some of the highest rates of nest success (Johnson pecker nests at Cedar Creek Ecosystem Science Reserve in and Kermott 1994). A review of woodpecker nesting ecology East Bethel, MN with a nest cavity camera (IBWO.org, Little across species documented nest success ranging from 0.42 to Rock, Arkansas) and telescoping pole (Crain, Mound City, Il- 1.00 with a median of 0.80 (n = 84 populations), and that pre- linois). -
A Supplemental Bibliography of Herpetology in New Mexico
A Supplemental Bibliography of Herpetology in New Mexico --- Revised: 1 September 2005 --- Compiled by: James N. Stuart New Mexico Department of Game & Fish Conservation Services Division P.O. Box 25112 , Santa Fe, NM 87504-5112 and Curatorial Associate (Amphibians & Reptiles) Museum of Southwestern Biology University of New Mexico E-mail: [email protected] This document may be cited as: Stuart, J.N. 2005. A Supplemental Bibliography of Herpetology in New Mexico. Web publication (Revised: 1 September 2005): http://www.msb.unm.edu/herpetology/publications/stuart_supl_biblio.pdf Contents Section 1: Introduction and Acknowledgments Section 2: Alphabetical List of References Section 3: Index of References by Taxon or General Topic Appendix A: List of Standard English and Current Scientific Names for Amphibians and Reptiles of New Mexico Appendix B: List of State and Federally Protected Herpetofauna in New Mexico Section 1: Introduction and Acknowledgments The publication of Amphibians and Reptiles of New Mexico by W.G. Degenhardt, C.W. Painter, and A.H. Price in 1996 provided the first comprehensive review of the herpetofauna in New Mexico. Approximately 1,600 references were cited in the book and yet, as is the nature of scientific research, additional information continues to be published on the amphibian and reptile populations of this state. This supplemental bibliography was created to build on the information in Degenhardt et al. by compiling all pertinent references not included in their 1996 book or in their corrigenda to the book (Price et al. 1996). References include both peer-reviewed and non-reviewed (e.g., “gray literature”) sources such as journal and magazine articles, books, book chapters, symposium proceedings, doctoral dissertations, master’s theses, unpublished agency and contract reports, and on-line Web publications. -
Where Are Shortgrass Prairies in Wyoming? Basically, Shortgrass Prairie Is Found in the Eastern One-Third of Wyoming, in the Rain Shadow of the Rocky Mountains
Shortgrass Prairie Ecosystem Flashcards Shortgrass Prairie What is a shortgrass prairie? Short grass prairie habitat is flat to rolling terrain dominated by short grasses that form a nearly continuous carpet across the landscape. Grama grass and buffalo grass make up 70% to 90% of the plants growing on the short grass prairie. A few mid-grasses and forbs also grow there. Short grass prairie s is the westernmost and driest of the true North American grasslands. Average annual precipitation is 10 to 12 inches. Why are shortgrass prairies important? Shortgrass prairies provide essential habitat for many species of wildlife that live nowhere else. Grazing buffalo, deer, and pronghorn as well as burrowing mammals are the iconic animals of this landscape. However, the grasses are the real star of this ecosystem. They can withstand the harsh climate better than any other plants and help to protect the essential topsoil. Without the grasses, we’d have no plant or animal life, just dust. Where are shortgrass prairies in Wyoming? Basically, shortgrass prairie is found in the eastern one-third of Wyoming, in the rain shadow of the Rocky Mountains. It becomes and replaced by sagebrush grasslands and foothills shrub land as the terrain rises westward toward the Rocky Mountains. rockies.audubon.org plt.wyomingplt.org Shortgrass Prairie Ecosystem Flashcards American Badger Black-tailed Jackrabbit Swift Fox Northern Pocket Gopher Ferruginous Hawk Short-eared Owl Page 1 A rockies.audubon.org plt.wyomingplt.org Shortgrass Prairie Ecosystem Flashcards Western -
Okanagan Ecoregional Assessment Volume 1 Report
VOLUME Okanagan 1 Ecoregional Assessment REPORT October 2006 OKANAGAN ECOREGIONAL ASSESSMENT VOLUME 1 REPORT Okanagan Ecoregional Assessment October 2006 Prepared by Nature Conservancy of Canada The Nature Conservancy of Washington and the Washington Department of Fish and Wildlife OKANAGAN ECOREGIONAL ASSESSMENT VOLUME 1 REPORT Okanagan Ecoregional Assessment Volume 1 – Report Citation: Pryce, B., P. Iachetti, G. Wilhere, K. Ciruna, J. Floberg, R. Crawford, R. Dye, M. Fairbarns, S. Farone, S. Ford, M. Goering, M. Heiner, G. Kittel, J. Lewis, D. Nicolson, and N. Warner. 2006. Okanagan Ecoregional Assessment, Volume 1 – Report. Prepared by Nature Conservancy of Canada, The Nature Conservancy of Washington, and the Washington Department of Fish and Wildlife with support from the British Columbia Conservation Data Centre, Washington Department of Natural Resources Natural Heritage Program, and NatureServe. Nature Conservancy of Canada, Victoria, British Columbia. Cover Design: Paul Mazzucca Copyright © 2006 Nature Conservancy of Canada Vancouver, British Columbia Issued by: The Nature Conservancy of Canada Cover Photo Credits: #300 – 1205 Broad Street Methow Valley, Robin Dye; Western screech owl, Victoria, British Columbia, Canada V8W 2A4 A.M. Bezener/One Wild Earth Photography; Great Email: [email protected] basin spadefoot toad, A.M. Bezener/One Wild Earth Photography; Seton Lake, Ian Routley; Canadian Cataloguing in Publication Data: Townsends big-eared bat, Harry van Oort; Mormon metalmark, Orville Dyer; East Chopaka, ISBN 1-897386-00-1 Barbara Pryce; Mountain bluebird, Ian Routley; 1. Biological inventory and assessment – Sockeye salmon, Kristy Ciruna; Badgers, Philippe Okanagan. Verkerk; Lynx, Grant Merrill; Mountain lady’s I. Nature Conservancy of Canada. slipper, George Thornton; Long-billed curlew, Ian II. -
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). -
Observation of a Gopher Snake (Pituophis Catenifer)Constricting a Red-Tailed Hawk (Buteo Jamaicensis)
LETTERS J. Raptor Res. 46(3):000–000 E 2012 The Raptor Research Foundation, Inc. OBSERVATION OF A GOPHER SNAKE (PITUOPHIS CATENIFER)CONSTRICTING A RED-TAILED HAWK (BUTEO JAMAICENSIS) KEY WORDS: Red-tailed Hawk; Buteo jamaicensis; gopher snake; Pituophis catenifer; predation. On 5 September 2008 at 0928 H, I observed an approxi- mately 1.6-m (total length) gopher snake (Pituophis cateni- fer) constricting an adult Red-tailed Hawk (Buteo jamaicensis) on the side of Forest Road 10 in the Cibola National Forest near Magdalena, New Mexico, U.S.A. (34u10.389N, 107u25.059W), at an elevation of 2265 m asl. After approach- ing the snake, I noticed that the hawk was still alive but struggling to breathe, as it was immobilized by the snake (Fig. 1). The snake had coils around the throat, chest, and wings of the hawk. The Red-tailed Hawk did not have the gopher snake grasped in its talons or in its bill, and the snake did not have any visible external injuries. When I approached, the snake exhibited typical defensive behavior, including hissing and striking toward me (Sweet 1985, Young et al. 1995). Approximately 12 min (0940 H) after I began my observation, the snake released the hawk, per- Figure 1. Gopher snake constricting a Red-tailed Hawk haps due to my close proximity. Now released, the hawk on 5 September 2008 near Magdalena, New Mexico, U.S.A. quickly stood up, spread its wings, and stood back about 2 m from the snake for approximately 30 sec. It then flew first indication that gopher snakes may possibly represent into a dead tree 10 m away, where it rested for 2 min, before an occasional source of mortality for healthy adult Red- it flew off the side of the hill and out of view.