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Reptile Collection Application
Utah Division of Wildlife Resources Application for Reptile Collection Certificate of Registration Applications must be received through mail, email, or in person at the DWR Salt Lake Office Only by January 19, 2018 5:00 pm. Utah Division of Wildlife Resources, ATTN: Wildlife Registration Office, PO Box 146301; 1594 W North Temple, Ste. 2110; Salt Lake City, UT 84114-6301 or email [email protected]. There is a $10.00 non-refundable handling fee and must be included when submitting application. You may enclose a check or money order payable to DWR, pay in person at a Division Office or arrange to make a credit card payment over the phone. Please list your phone number here to arrange payment by phone. The $75.00 Certificate of Registration fee will be collected from successful applicants upon approval. If necessary, a drawing will be conducted for those species that have more applications than available permits on January 24. Remaining permits will be available January 25 on a first-come, first-served basis at the DWR Salt Lake Office. Name________________________________ Phone_______________________ Email________________________ Address____________________________ City___________________ State________ ZIP________________ Date of Birth___________________________ Limit Total Collection Species per Authorized County Permits Season County California Kingsnake 6 2 Garfield, Kane, and San Juan March 1 - Oct 31 Daggett, Duchesne, Salt Lake, Summit, Smooth Greensnake 6 1 March 1 - Oct 31 Utah, Uintah, Wasatch, and Weber Beaver, Daggett, -
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. -
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. amphibian-reptile-conservation.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. -
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. -
Life History Account for Western Threadsnake
California Wildlife Habitat Relationships System California Department of Fish and Wildlife California Interagency Wildlife Task Group WESTERN THREADSNAKE Rena humilis Family: LEPTOTYPHLOPIDAE Order: SQUAMATA Class: REPTILIA R045 Written by: R. Marlow Reviewed by: T. Papenfuss Edited by: R. Duke, J. Harris DISTRIBUTION, ABUNDANCE, AND SEASONALITY The western threadsnake (once known as the western blind snake) is widely distributed in southern California from the coast to the eastern border at elevations up to 1515 m (5000 ft). It seldom occurs in strictly sandy areas, alluvial flats or dry lakes. Little is known about abundance. A wide variety of habitats at lower elevations is occupied where conditions are suitable for burrowing, or hiding under surface objects and in crevices (Klauber 1940, Brattstrom 1953, Brattstrom and Schwenkmeyer 1951, Stebbins 1954, 1972). SPECIFIC HABITAT REQUIREMENTS Feeding: This snake eats ants, termites, their eggs, larvae and other soft-bodied insects (Stebbins 1954). Cover: This snake burrows, spending most of its time underground. It has also been taken under objects such as logs, rocks and among the roots of shrubs. They have also been taken under granite flakes (Stebbins 1954). Reproduction: No data. Water: The species seems to prefer moister habitats but is found in very arid environments, so permanent water is probably not required (Stebbins 1954). Pattern: This species prefers moist areas. In canyons, stony and sandy deserts, rocky slopes and boulder piles, and scrub. SPECIES LIFE HISTORY Activity Patterns: This snake appears on the surface at night but may be active underground at other times. Greatest seasonal activity occurs from April to August (Stebbins 1954). -
Life History of the Coppertail Skink (Ctenotus Taeniolatus) in Southeastern Australia
Herpetological Conservation and Biology 15(2):409–415. Submitted: 11 February 2020; Accepted: 19 May 2020; Published: 31 August 2020. LIFE HISTORY OF THE COPPERTAIL SKINK (CTENOTUS TAENIOLATUS) IN SOUTHEASTERN AUSTRALIA DAVID A. PIKE1,2,6, ELIZABETH A. ROZNIK3, JONATHAN K. WEBB4, AND RICHARD SHINE1,5 1School of Biological Sciences A08, University of Sydney, New South Wales 2006, Australia 2Present address: Department of Biology, Rhodes College, Memphis, Tennessee 38112, USA 3Department of Conservation and Research, Memphis Zoo, Memphis, Tennessee 38112, USA 4School of Life Sciences, University of Technology Sydney, Broadway, New South Wales 2007, Australia 5Present address: Department of Biological Sciences, Macquarie University, New South Wales 2109, Australia 6Corresponding author, e-mail: [email protected] Abstract.—The global decline of reptiles is a serious problem, but we still know little about the life histories of most species, making it difficult to predict which species are most vulnerable to environmental change and why they may be vulnerable. Life history can help dictate resilience in the face of decline, and therefore understanding attributes such as sexual size dimorphism, site fidelity, and survival rates are essential. Australia is well-known for its diversity of scincid lizards, but we have little detailed knowledge of the life histories of individual scincid species. To examine the life history of the Coppertail Skink (Ctenotus taeniolatus), which uses scattered surface rocks as shelter, we estimated survival rates, growth rates, and age at maturity during a three-year capture-mark- recapture study. We captured mostly females (> 84%), and of individuals captured more than once, we captured 54.3% at least twice beneath the same rock, and of those, 64% were always beneath the same rock (up to five captures). -
Amphibian Alliance for Zero Extinction Sites in Chiapas and Oaxaca
Amphibian Alliance for Zero Extinction Sites in Chiapas and Oaxaca John F. Lamoreux, Meghan W. McKnight, and Rodolfo Cabrera Hernandez Occasional Paper of the IUCN Species Survival Commission No. 53 Amphibian Alliance for Zero Extinction Sites in Chiapas and Oaxaca John F. Lamoreux, Meghan W. McKnight, and Rodolfo Cabrera Hernandez Occasional Paper of the IUCN Species Survival Commission No. 53 The designation of geographical entities in this book, and the presentation of the material, do not imply the expression of any opinion whatsoever on the part of IUCN concerning the legal status of any country, territory, or area, or of its authorities, or concerning the delimitation of its frontiers or boundaries. The views expressed in this publication do not necessarily reflect those of IUCN or other participating organizations. Published by: IUCN, Gland, Switzerland Copyright: © 2015 International Union for Conservation of Nature and Natural Resources Reproduction of this publication for educational or other non-commercial purposes is authorized without prior written permission from the copyright holder provided the source is fully acknowledged. Reproduction of this publication for resale or other commercial purposes is prohibited without prior written permission of the copyright holder. Citation: Lamoreux, J. F., McKnight, M. W., and R. Cabrera Hernandez (2015). Amphibian Alliance for Zero Extinction Sites in Chiapas and Oaxaca. Gland, Switzerland: IUCN. xxiv + 320pp. ISBN: 978-2-8317-1717-3 DOI: 10.2305/IUCN.CH.2015.SSC-OP.53.en Cover photographs: Totontepec landscape; new Plectrohyla species, Ixalotriton niger, Concepción Pápalo, Thorius minutissimus, Craugastor pozo (panels, left to right) Back cover photograph: Collecting in Chamula, Chiapas Photo credits: The cover photographs were taken by the authors under grant agreements with the two main project funders: NGS and CEPF. -
Multi-National Conservation of Alligator Lizards
MULTI-NATIONAL CONSERVATION OF ALLIGATOR LIZARDS: APPLIED SOCIOECOLOGICAL LESSONS FROM A FLAGSHIP GROUP by ADAM G. CLAUSE (Under the Direction of John Maerz) ABSTRACT The Anthropocene is defined by unprecedented human influence on the biosphere. Integrative conservation recognizes this inextricable coupling of human and natural systems, and mobilizes multiple epistemologies to seek equitable, enduring solutions to complex socioecological issues. Although a central motivation of global conservation practice is to protect at-risk species, such organisms may be the subject of competing social perspectives that can impede robust interventions. Furthermore, imperiled species are often chronically understudied, which prevents the immediate application of data-driven quantitative modeling approaches in conservation decision making. Instead, real-world management goals are regularly prioritized on the basis of expert opinion. Here, I explore how an organismal natural history perspective, when grounded in a critique of established human judgements, can help resolve socioecological conflicts and contextualize perceived threats related to threatened species conservation and policy development. To achieve this, I leverage a multi-national system anchored by a diverse, enigmatic, and often endangered New World clade: alligator lizards. Using a threat analysis and status assessment, I show that one recent petition to list a California alligator lizard, Elgaria panamintina, under the US Endangered Species Act often contradicts the best available science. -
2008 Amphibian Distribution Surveys in Wadeable Streams and Ponds in Western and Southeast Oregon
INFORMATION REPORTS NUMBER 2010-05 FISH DIVISION Oregon Department of Fish and Wildlife 2008 Amphibian Distribution Surveys in Wadeable Streams and Ponds in Western and Southeast Oregon Oregon Department of Fish and Wildlife prohibits discrimination in all of its programs and services on the basis of race, color, national origin, age, sex or disability. If you believe that you have been discriminated against as described above in any program, activity, or facility, or if you desire further information, please contact ADA Coordinator, Oregon Department of Fish and Wildlife, 3406 Cherry Drive NE, Salem, OR, 503-947-6000. This material will be furnished in alternate format for people with disabilities if needed. Please call 541-757-4263 to request 2008 Amphibian Distribution Surveys in Wadeable Streams and Ponds in Western and Southeast Oregon Sharon E. Tippery Brian L. Bangs Kim K. Jones Oregon Department of Fish and Wildlife Corvallis, OR November, 2010 This project was financed with funds administered by the U.S. Fish and Wildlife Service State Wildlife Grants under contract T-17-1 and the Oregon Department of Fish and Wildlife, Oregon Plan for Salmon and Watersheds. Citation: Tippery, S. E., B. L Bangs and K. K. Jones. 2010. 2008 Amphibian Distribution Surveys in Wadeable Streams and Ponds in Western and Southeast Oregon. Information Report 2010-05, Oregon Department of Fish and Wildlife, Corvallis. CONTENTS FIGURES....................................................................................................................................... -
BACKGROUND ENVIRONMENTAL REPORT Existing Conditions | January 2020
Thousand Oaks BACKGROUND ENVIRONMENTAL REPORT Existing Conditions | January 2020 EXISTING CONDITIONS REPORT: BACKGROUND ENVIRONMENTAL Age, including mastodon, ground sloth, and saber-toothed cat CHAPTER 1: CULTURAL (City of Thousand Oaks 2011). RESOURCES Native American Era The earliest inhabitants of Southern California were transient hunters visiting the region approximately 12,000 B.C.E., who were the cultural ancestors of the Chumash. Evidence of significant and Cultural Setting continuous habitation of the Conejo Valley region began around The cultural history of the City of Thousand Oaks and the 5,500 B.C.E. Specifically, during the Millingstone (5,500 B.C.E – surrounding Conejo Valley can be divided in to three major eras: 1,500 B.C.E.) and the Intermediate (1,500 B.C.E. – 500 C.E.) Native-American, Spanish-Mexican, and Anglo-American. periods, the Conejo Valley experienced a year-round stable Remnants from these unique eras exist in the region as a diverse population of an estimated 400-600 people. During this time, range of tribal, archaeological and architectural resources. The people typically lived in largely open sites along water courses Conejo Valley served as an integral part of the larger Chumash and in caves and rock shelters; however, a number of site types territory that extended from the coast and Channel Islands to have been discovered, including permanent villages, semi- include Santa Barbara, most of Ventura, parts of San Luis Obispo, permanent seasonal stations, hunting camps and gathering Kern and Los Angeles Counties. The late 18th and early 19th localities focused on plant resources (City of Thousand Oaks 2011). -
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. -
02186714 Colombia Finalrepo
2 TABLE OF CONTENTS Project partners & Collaborators ...................................................................................................................................... 3 SECTION 1 ....................................................................................................................................................................... 4 Summary ............................................................................................................................................................................... 4 Introduction ......................................................................................................................................................................... 4 Project members ................................................................................................................................................................. 6 SECTION 2 .....................................................................................................................................................................10 Aim and objectives ......................................................................................................................................................10 Changes to original project plan ...............................................................................................................................10 Methodology ................................................................................................................................................................11