Reptiles in Managed Woodlands

Total Page:16

File Type:pdf, Size:1020Kb

Reptiles in Managed Woodlands Woodland Fish & Wildlife • 2020 Reptiles in Managed Woodlands Tools for Family Forestland Owners Authors: Eliana Pool, Cafferata Consulting; Barbara Garcia, United States Forest Service; Susan Barnes, Oregon Department of Fish and Wildlife, Lauren Grand, Oregon State University Forestry Extension; and Jennifer Weikel, Oregon Department of Forestry Introduction Western Pond Turtle Reptiles are some of the most ancient and interesting animals on earth. Not only do they remind us of their dinosaur relatives, but reptiles are of great ecological impor- tance, serving critical roles in ecosystems. They are found on all continents, except Antarctica and there are 29 distinct species of reptiles found in Oregon and Washing- ton. They occur in upland (dry), aquatic (wet), or a combination of these habitats. They are both prey (eaten by fish, mam- mals, birds, and other reptiles) and preda- tors (eating insects, snails, slugs, worms, amphibians, other reptiles, and small mammals). The reptiles group includes a variety of species such as turtles (e.g., western pond turtle), lizards (e.g., western Photo by Keith Kohl fence lizard), and snakes (e.g., rubber boa). Reptiles may also provide species manage- growth and reproduction, and helps reptiles found in forested habitats in ment and disease control by eating animals them adapt to periodic shortages of food, Oregon and Washington and will describe such as rodents and slugs. water, and oxygen. Reptiles have limited common threats and management rec- Reptiles are scaly ectotherms, or cold- capability to move quickly out of harm’s ommendations to help provide for these blooded animals, who regulate their way, travel long distances or across bar- remarkable animals. Knowing the differ- internal temperature by the external riers such as roads, rivers, and developed ence between reptiles and amphibians can environment. Their specialized physiology landscapes. They often spend most of be confusing. Our callout box explains allows for more energy to be put toward their time at specific breeding locations or the differences. over-wintering sites to which they return Western Fence Lizard year after year, following particular migra- Rubber Boa Snake tion routes. These characteristics make reptiles sensitive to habitat loss, degrada- tion, fragmentation, and to disturbances at breeding and over-wintering sites. Woodland owners in Oregon and Wash- ington can promote habitat for reptiles on their property and improve overall ecosys- tem health. This publication focuses on Photo by Keith Kohl Photo by Simon Wray 1 Woodland Fish & Wildlife • 2020 Physical Traits Amphibian Reptile Smooth, moist and sometimes sticky Dry and scaly. Scales are made of keratin. Skin Texture skin. Laden with mucous glands. Skin is found underneath the scales. Have soft gel surrounding their eggs Amniotic egg. Have hard, leathery eggs Eggs/Young without any hard covering. Usually, laid on land or they keep eggs in their found in water or damp places. bodies until they hatch. Short fore limbs and long hind limbs Reptiles usually have four limbs, but some Limbs with four or five webbed digits. reptiles (snakes) have no limbs. Yes. Breathes water through gills until it No. Looks like a miniature adult when Metamorphosis* develops lungs. born. Method of breathing Gills and lungs Lungs Nails and teeth (some have venom). Toxic skin secretions and can bite. No Defense Reptiles have scales, which act as armor to nails. physically defend the body. Examples Frog, toad, newts, salamanders Snakes, lizards, turtles *Metamorphosis is the process of transformation from an immature form to an adult form in two or more distinct stages. Habitat pond turtle spends the winter buried under Many reptiles have periods of dormancy. Reptiles are found in forests, deserts, grass- leaf litter in forested habitats, sometimes This means that their bodies shut down lands, lakes, and everywhere in between. at the base of trees or near logs. When and conserve energy for the coming year. For many reptiles the utilization of a variety reptiles lay eggs, they need to find warm During this time, they may not eat, drink, of habitats is critical for their success, discrete hiding places, usually in sparsely defecate or move for several weeks. In the although populations and species diversity vegetated areas including forest edges and winter this dormancy period is referred are typically higher in dry sunny regions forest openings. Some snakes and lizards to as hibernation and in the summer, it is than in cooler, more temperate zones. lay their eggs in rock crevices or in empty called aestivation. rodent burrows. Others deposit their eggs Since reptiles are cold-blooded animals in or under rotting stumps or logs where Upland Habitats and therefore use the sun to thermoregu- the heat of the decomposing plant material late, they often bask in sunny places. All species of reptiles in Oregon and Wash- incubates the eggs. Thermoregulation is a process that allows ington use upland habitats, and for some, reptiles to maintain their basic metabolic it is the only habitat they will use over the course of their lifetime. Upland habitats, processes (Pilliod et. al. 2017). Reptiles Western Painted Turtle need help to maintain their body tempera- including forests, are very diverse and have tures in the right range to enable them to key habitat elements that meet various eat, hide, move, mate, nest and lay eggs critical life history needs like foraging and to keep their bodily functions work- areas and places to nest, lay eggs, and raise ing properly. The sun also helps them young. During periods of dormancy, rep- maintain healthy levels of vitamins and tiles may be found in many places within minerals. Both aquatic and upland habitat forested environments. For example, basking areas are important for reptiles. Northern alligator lizards will seek refuge They are so important, western painted under downed wood in coniferous forests. turtles have been observed using the backs Other forest habitat features used by rep- of loons to bask (Gelatt and Kelley 1995). tiles include abandoned mammal burrows, leaf litter, soil, and bark. Staying warm is a way of life for a reptile. For example, in cool wet places the western Photo by Scott Fitkin, WDFW 2 Woodland Fish & Wildlife • 2020 Forests are an important aspect of reptile habitat for some reptiles, they are gener- life history because they provide a less vari- It is well known that reptiles ally less desirable than natural habitats. able microclimate that protects dormant are known for needing lots of reptiles from harsh conditions. It is estimat- sunshine. However, did you Often on warm, sunny days turtles and ed that reptiles can reduce their energy use know that reptiles can overheat snakes can be seen lounging on logs by 90-95% during dormant phases, which too? Reptiles have no way to and other exposed objects that are cool down like people do and becomes a vital survival instinct during partially submerged in the water like must find shade or some way to particularly cold winters or during sum- rocks, fallen limbs, and floating vegeta- escape extreme heat. Reptiles tion. These basking sites are necessary mers with prolonged periods of drought have varying degrees of heat and high temperatures (ODFW 2015). for thermoregulation and also provide tolerances. protection from predators such as bass Aquatic Habitats and other large fish. Garter snakes are Some reptiles require aquatic habitats floodplains, and riparian fringes. Although often found in and near water and will too! Aquatic habitats include wetlands, artificial features such as fire and irrigation sometimes swim to hunt frogs and even rivers, streams, lakes, ponds, sloughs, ponds and ditches can provide aquatic fish. On cooler days, when cloud cover and Table1. Native Reptiles found in forested habitats of Oregon and Washington Species Range Habitat Turtles Eastern OR and WA; Found in slow-moving or still water (ponds, Western painted turtle* Columbia River in OR and sloughs, streams, rivers and oxbow lakes) with (Chrysemys picta bellii) WA; Puget Sound and mucky bottoms, floodplain woodlands, shrubby Willamette Valley fields, roadsides, pastures, and open beaches. Found in permanent and intermittent waters in- Willamette Valley, Coast cluding marshes, streams, rivers, ponds and lakes. Western pond turtle* Range and SW OR; Usually with areas of large amounts of vegetation (Clemmys marmorata) Columbia Plateau OR and and basking sites. Require upland areas adjacent WA, Puget Sound WA to water for egg laying and overwintering refugia. Require nearby forested areas for overwintering Lizards and Skinks Often found in moist meadows in coniferous Northern alligator lizard Western OR and WA forests and riparian areas, oak-pine forest and (Elgaria coerulea) and eastern WA. forest edges. Found in grasslands, chaparral, oak woodlands, Southern alligator lizard Western OR and WA as edges of coniferous forests, riparian zones, and (Elgaria multicarinata) well as in northcentral OR moist canyon bottoms. Throughout OR except Found in desert canyons, grasslands, hard- Western fence lizard the Coast Range and high wood and coniferous forests, rocky areas and (Sceloporus occidentalis) cascades; Puget Sound chaparral. Lowland, and central WA Mostly throughout OR Western skink Found in oak woodlands, less damp coniferous except coastal areas and (Eumeces skiltonianus) forests, pine and juniper woodlands. high elevations; eastern WA 3 Woodland Fish & Wildlife • 2020 Species Range Habitat Snakes Throughout most of OR Found in a wide variety of habitats. Usually Rubber boa and WA except the most occur in close proximity to water. In forests use (Charina bottae) coastal areas and some logs, bark, flat rocks, crevices, and forest litter. sagebrush areas. Throughout OR except the Found in sagebrush flats, juniper woodlands, Racer Coast and Cascade ranges chaparral, meadows, and fields where rocks, (Coluber constrictor) and eastern WA logs, or dense shrubs are present. OR Coast Range and the Sharptail snake Found in oak woodlands, river valleys and Willamette Valley and the (Contia tenuis) canyons.
Recommended publications
  • Evidence of Lingual-Luring by an Aquatic Snake
    Journal of Herpetology, Vol. 34 No. 1 pp 67-74, 2000 Copyright 2000 Society for the Study of Amphibians and Reptiles Evidence of Lingual-luring by an Aquatic Snake HARTWELL H. WELSH, JR. AND AMY J. LIND Pacific Southwest Research Station, USDA Forest Service, 1700 Bayview Dr., Arcata, California 95521, USA. E-mail: hwelsh/[email protected] ABSTRACT.-We describe and quantify the components of an unusual snake behavior used to attract fish prey: lingual-luring. Our earlier research on the foraging behavior of the Pacific Coast aquatic garter snake (Thamnophis atratus) indicated that adults are active foragers, feeding primarily on aquatic Pacific giant salamanders (Dicamptodon tenebrosus) in streambed substrates. Juvenile snakes, however, use primarily ambush tactics to capture larval anurans and juvenile salmonids along stream margins, behaviors that include the lingual-luring described here. We found that lingual-luring differed from typical chemosensory tongue-flicking by the position of the snake, contact of the tongue with the water surface, and the length of time the tongue was extended. Luring snakes are in ambush position and extend and hold their tongues out rigid, with the tongue-tips quivering on the water surface, apparently mimicking insects in order to draw young fish within striking range. This behavior is a novel adaptation of the tongue-vomeronasal system by a visually-oriented predator. The luring of prey by snakes has been asso- luring function (Mushinsky, 1987; Ford and ciated primarily with the use of the tail, a be- Burghardt, 1993). However, Lillywhite and Hen- havior termed caudal luring (e.g., Neill, 1960; derson (1993) noted the occurrence of a pro- Greene and Campbell, 1972; Heatwole and Dav- longed extension of the tongue observed in vine ison, 1976; Jackson and Martin, 1980; Schuett et snakes (e.g., Kennedy, 1965; Henderson and al., 1984; Chizar et al., 1990).
    [Show full text]
  • Ecology of the Cascades Frog (Rana Cascadae)
    Ecology of the Cascades Frog ( Rana cascadae) and Interactions with Garter Snakes and Nonnative Trout in the Trinity Alps Wilderness, California By: Justin M. Garwood and Hartwell H. Welsh Jr. December 2007 Final Report To: California Department of Fish and Game National Fish and Wildlife Foundation Habitat Conservation Planning Branch Bring Back The Natives Grant Program 1416 Ninth Street, Suite 1280 and 1120 Connecticut Avenue NW, Suite 900 Sacramento, CA 95814 Washington, DC 20036 Amphibian Specialist Group i Cascades Frog Ecology in California Cover Photos: Adult female Cascades frog ( Rana cascadae ), aquatic garter snake ( Thamnophis atratus ) captured in Echo Lake basin regurgitating an Eastern brook trout ( Salvelinus fontinalis ), surveying Atlantis meadows west of Red Mountain summit, Trinity Alps Wilderness, California. ( Photos: J. Garwood ) ii Cascades Frog Ecology in California ECOLOGY OF THE CASCADES FROG ( RANA CASCADAE ) AND INTERACTIONS WITH GARTER SNAKES AND NONNATIVE TROUT IN THE TRINITY ALPS WILDERNESS, CALIFORNIA December 2007 FINAL REPORT TO THE CALIFORNIA DEPARTMENT OF FISH AND GAME AND NATIONAL FISH AND WILDLIFE FOUNDATION DFG CONTRACT NO. P0385107 NFWF CONTRACT NO. 2004-0075-000, Bring Back The Natives Grant Administered By: Humboldt State University Sponsored Programs Foundation P.O. Box 1185 Arcata, CA 95518-1185 PRINCIPAL INVESTIGATORS: Justin M. Garwood and Hartwell H. Welsh, Jr. USDA Forest Service Pacific Southwest Research Station Redwood Sciences Laboratory 1700 Bayview Dr. Arcata, CA 95521 STATE OF CALIFORNIA CONTRACT MANAGER Betsy Bolster Staff Environmental Scientist Department of Fish and Game Wildlife Branch 1416 Ninth Street, Suite 1280 Sacramento, CA 95814 iii Cascades Frog Ecology in California ECOLOGY OF THE CASCADES FROG ( RANA CASCADAE ) AND INTERACTIONS WITH GARTER SNAKES AND NONNATIVE TROUT IN THE TRINITY ALPS 1/ WILDERNESS, CALIFORNIA December, 2007 By Justin M.
    [Show full text]
  • Garter Snake Population Dynamics from a 16-Year Study: Considerations for Ecological Monitoring
    Ecological Applications, 15(1), 2005, pp. 294±303 q 2005 by the Ecological Society of America GARTER SNAKE POPULATION DYNAMICS FROM A 16-YEAR STUDY: CONSIDERATIONS FOR ECOLOGICAL MONITORING AMY J. LIND,1 HARTWELL H. WELSH,JR., AND DAVID A. TALLMON2 USDA Forest Service, Paci®c Southwest Research Station, Redwood Sciences Laboratory, 1700 Bayview Drive, Arcata, California 95521 USA Abstract. Snakes have recently been proposed as model organisms for addressing both evolutionary and ecological questions. Because of their middle position in many food webs they may be useful indicators of trophic complexity and dynamics. However, reliable data on snake populations are rare due to the challenges of sampling these patchily distributed, cryptic, and often nocturnal species and also due to their underrepresentation in the eco- logical literature. Studying a diurnally active stream-associated population of garter snakes has allowed us to avoid some of these problems so that we could focus on issues of sampling design and its in¯uence on resulting demographic models and estimates. From 1986 to 2001, we gathered data on a population of the Paci®c coast aquatic garter snake (Thamnophis atratus) in northwestern California by conducting 3±5 surveys of the population annually. We derived estimates for sex-speci®c survival rates and time-dependent capture probabilities using population analysis software and examined the relationship between our calculated capture probabilities and variability in sampling effort. We also developed population size and density estimates and compared these estimates to simple count data (often used for wildlife population monitoring). Over the 16-yr period of our study, we marked 1730 snakes and had annual recapture rates ranging from 13% to 32%.
    [Show full text]
  • Snake Surveys in Jackson, Josephine and Southern Douglas Counties, Oregon
    Snake Surveys in Jackson, Josephine and Southern Douglas Counties, Oregon JASON REILLY ED MEYERS DAVE CLAYTON RICHARD S. NAUMAN May 5, 2011 For more information contact: Jason Reilly Medford District Bureau of Land Management [email protected] Introduction Southwestern Oregon is recognized for its high levels of biological diversity and endemism (Whittaker 1961, Kaye et al. 1997). The warm climate and broad diversity of habitat types found in Jackson and Josephine counties result in the highest snake diversity across all of Oregon. Of the 15 snake species native to Oregon, 13 occur in the southwestern portion of the state and one species, the night snake, is potentially found here. Three of the species that occur in Oregon: the common kingsnake, the California mountain kingsnake, and the Pacific Coast aquatic garter snake are only found in southwestern Oregon (Table 1, St. John 2002). Table 1. Snakes known from or potentially found in Southwestern Oregon and conservation status. Scientific Name Common Name Special Status Category1 Notes Charina bottae Rubber Boa None Common Sharp-tailed See Feldman and Contia tenuis None Snake Hoyer 2010 Recently described Forest Sharp-tailed Contia longicaudae None species see Feldman Snake and Hoyer 2010 Diadophis Ring-necked Snake None punctatus Coluber constrictor Racer None Masticophis Appears to be very Stripped Whipsnake None taeniatus rare in SW Oregon Pituophis catenifer Gopher Snake None Heritage Rank G5/S3 Lampropeltis Federal SOC Appears to be rare in Common Kingsnake getula ODFW SV SW Oregon ORBIC 4 Heritage Rank G4G5/S3S4 Lampropeltis California Mountain Federal SOC zonata Kingsnake ODFW SV ORBIC 4 Thamnophis sirtalis Common Garter Snake None Thamnophis Northwestern Garter None ordinoides Snake Thamnophis Western Terrestrial None elegans Garter Snake Thamnophis Pacific Coast Aquatic None atratus Garter Snake No records from SW Hypsiglena Oregon.
    [Show full text]
  • Morphological and Ecological Convergence in Two Natricine Snakes
    Blackwell Science, LtdOxford, UKBIJBiological Journal of the Linnean Society0024-4066The Linnean Society of London, 2005? 2005 85? 363371 Original Article CONVERGENCE IN NATRICINE SNAKES T. J. HIBBITTS and L. A. FITZGERALD Biological Journal of the Linnean Society, 2005, 85, 363–371. With 4 figures Morphological and ecological convergence in two natricine snakes TOBY J. HIBBITTS* and LEE A. FITZGERALD Department of Wildlife and Fisheries Sciences, Texas A & M University, College Station, TX 77843–2258, USA Received 23 February 2004; accepted for publication 27 September 2004 Similar morphologies between species may be due to shared ancestry or convergent evolution. Understanding instances of morphological and ecological convergence is central to evolutionary ecology because they help us under- stand the fit between organism and environment. Two species of stream-dwelling natricine snakes, Thamnophis rufipunctatus and Nerodia harteri present a model system for studying ecological and morphological convergence and adaptation. The species are allopatric and both live in shallow riffles in streams and forage visually for fish. We studied morphological similarity, trait evolution and functional significance of ecologically relevant traits in these and related species, and used mitochondrial DNA sequences for the ND4 gene to estimate their phylogenetic rela- tionships. Character mapping of head length and head width supported the hypothesis of independent evolution of head shape in T. rufipunctatus and N. harteri. The elongate snout is a derived trait in these two taxa that is asso- ciated with reduced hydrodynamic drag on the snakes’ heads when in a swift current, compared to other species with the ancestral blunt snout. We hypothesize that lower hydrodynamic drag facilitates prey capture success in these species that are known to forage by holding their position in currents and striking at fish prey.
    [Show full text]
  • Complete List of Amphibian, Reptile, Bird and Mammal Species in California
    Complete List of Amphibian, Reptile, Bird and Mammal Species in California California Department of Fish and Game Sept. 2008 (updated) This list represents all of the native or introduced amphibian, reptile, bird and mammal species known in California. Introduced species are marked with “I”, harvest species with “HA”, and vagrant species or species with extremely limited distributions with *. The term “introduced”, as used here, represents both accidental and intentional introductions. Subspecies are not included on this list. The most current list of species and subspecies with special management status is available from the California Natural Diversity Database (CNDDB) Taxonomy and nomenclature used within the list are the same as those used within both the CNDDB and CWHR software programs and data sets. If a discrepancy exists between this list and the ones produced by CNDDB, the CNDDB list can be presumed to be more accurate as it is updated more frequently than the CWHR data set. ________________________________________________________________________ ______________________________________________________________________ ______________________________________________________________________ AMPHIBIA (Amphibians) CAUDATA (Salamanders) AMBYSTOMATIDAE (Mole Salamanders and Relatives) Long-toed Salamander Ambystoma macrodactylum Tiger Salamander Ambystoma tigrinum I California Tiger Salamander Ambystoma californiense Northwestern Salamander Ambystoma gracile RHYACOTRITONIDAE (Torrent or Seep Salamanders) Southern Torrent Salamander Rhyacotriton
    [Show full text]
  • Thamnophis Sirtalis) Stomach Contents Detects Cryptic Range of a Secretive Salamander (Ensatina Eschscholtzii Oregonensis)
    Herpetological Conservation and Biology 5(3):395–402. Submitted: 28 July 2010; Accepted: 12 October 2010. PHYLOGENETIC ANALYSIS OF COMMON GARTER SNAKE (THAMNOPHIS SIRTALIS) STOMACH CONTENTS DETECTS CRYPTIC RANGE OF A SECRETIVE SALAMANDER (ENSATINA ESCHSCHOLTZII OREGONENSIS) 1,3 1,4 2 1,5 SEAN B. REILLY , ANDREW D. GOTTSCHO , JUSTIN M. GARWOOD , AND W. BRYAN JENNINGS 1Department of Biological Sciences, Humboldt State University, 1 Harpst St., Arcata, California 95521, USA 2Redwood Sciences Laboratory, Pacific Southwest Research Station, USDA Forest Service, 1700 Bayview Drive, Arcata, California 95521, USA 3Present Address: Museum of Vertebrate Zoology, 3101 Valley Life Sciences Building, University of California, Berkeley, California 94704, USA, email: [email protected] 4Present Address: Department of Biology, San Diego State University, 5500 Campanile Drive, San Diego, California 92182, USA 5Present Address: Universidade Federal do Rio de Janeiro, Museu Nacional, Departamento de Vertebrados, Rio de Janeiro, RJ, 20940-040, Brazil Abstract. Given the current global amphibian decline, it is crucial to obtain accurate and current information regarding species distributions. Secretive amphibians such as plethodontid salamanders can be difficult to detect in many cases, especially in remote, high elevation areas. We used molecular phylogenetic analyses to identify three partially digested salamanders palped from the stomachs of three Common Garter Snakes (Thamnophis sirtalis) from the Klamath Mountains in northern California. Our results conclusively show that the salamanders were all individuals of Ensatina eschscholtzii oregonensis, revealing a substantial vertical range extension for this sub-species, and documenting the first terrestrial breeding salamander living in the sub-alpine zone of the Klamath Mountains. Key Words. Common Garter Snake, distribution, Ensatina, Ensatina eschscholtzii, Klamath Mountains, mitochondrial DNA, Thamnophis sirtalis INTRODUCTION breeders.
    [Show full text]
  • Non-Native Fish in Mountain Lakes: Effects on a Declining Amphibian and Ecosystem Subsidy
    NON-NATIVE FISH IN MOUNTAIN LAKES: EFFECTS ON A DECLINING AMPHIBIAN AND ECOSYSTEM SUBSIDY Sharon P. Lawler and Karen L. Pope Department of Entomology, UC Davis Emails: [email protected] and [email protected] UC Water Resources Center Technical Completion Report Project No. W-987 October, 2006 Abstract Wilderness water resources often provide wildlife habitat and associated recreational opportunities, such as angling or birdwatching. Introduced trout in mountain lakes could affect terrestrial wildlife by changing ecosystem subsidy, which is the flow of nutrients and organisms from aquatic to terrestrial habitats. Trout prey upon larval amphibians and aquatic insects, and the adult stages of aquatic insects and amphibians are prey for bats, birds, snakes, and other terrestrial insectivores. The indirect effects of introduced fish on terrestrial wildlife have rarely been considered, and there have been no prior experiments testing effects of fish stocking on the Cascades frog (federal and California species of special concern). We conducted a four-year replicated whole-lake experiment to assess whether changes in fish abundance could aid frog recovery and whether trout predation of larval amphibians and aquatic invertebrates indirectly affects the density of terrestrial predators. Results show that non-native trout suppress the numbers of the declining Cascades frog and other amphibians, as well as large-bodied aquatic insects such as dragonflies and damselflies. After trout removals, these groups show a marked increase in abundance. We found differences in the species and abundance of garter snakes feeding at lakes with and without trout present. Over 100 species of birds and more than six species of bats use the lake basins during the snow-free season and we are currently assessing the data for patterns associated with trout abundances.
    [Show full text]
  • Inventory of Amphibians and Reptiles for Twelve National Parks in the Southern Colorado Plateau Network
    National Park Service Southern Colorado Plateau U.S. Department of the Interior Inventory and Monitoring Network Natural Resource Program Center Fort Collins, Colorado Inventory of Amphibians and Reptiles for Twelve National Parks in the Southern Colorado Plateau Network Trevor B. Persons and Erika M. Nowak USGS Southwest Biological Science Center, Colorado Plateau Research Station Northern Arizona University, Flagstaff, AZ 86011 April 2008 ON THE COVER Western Terrestrial Garter Snake from Walnut Canyon National Monument Photo by Trevor B. Persons PLEASE CITE THIS DOCUMENT AS: Nowak, E.M., and Trevor B. Persons. 2008. Inventory of Amphibians and Reptiles for Twelve National Parks in the Southern Colorado Plateau Network. Final report to the National Park Service, Southern Colorado Plateau Network, Flagstaff, AZ. Inventory of Amphibians and Reptiles for Twelve National Parks in the Southern Colorado Plateau Network Aztec Ruins National Monument Bandelier National Monument Chaco Culture National Historical Park El Malpais National Monument El Morro National Monument Glen Canyon National Recreation Area Petroglyph National Monument Salinas Pueblo Missions National Monument Sunset Crater National Monument Walnut Canyon National Monument Wupatki National Monument Yucca House National Monument Authors Trevor B. Persons and Erika M. Nowak USGS Southwest Biological Science Center, Colorado Plateau Research Station, Northern Arizona University, Flagstaff, AZ 86011 Project Manager Anne Cully National Park Service, Southern Colorado Plateau Network,
    [Show full text]
  • Jennings and Hayes 1994.Pdf
    AMPHIBIAN AND REPTILE SPECIES OF SPECIAL CONCERN IN CALIFORNIA Mark R. Jennings Research Associate Department of Herpetology, California Academy of Sciences Golden Gate Park, San Francisco, CA 94118-9961 and Marc P. Hayes Research Associate Department of Biology, Portland State University P.O. Box 751, Portland, OR 97207-0751 and Research Section, Animal Management Division, Metro Washington Park Zoo 4001 Canyon Road, Portland, OR 97221-2799 The California Department of Fish and Game commissioned this study as part of the Inland Fisheries Division Endangered Species Project. Specific recommendations from this study and in this report are made as options by the authors for the Department to consider. These recommendations do not necessarily represent the findings, opinions, or policies of the Department. FINAL REPORT SUBMITTED TO THE CALIFORNIA DEPARTMENT OF FISH AND GAME INLAND FISHERIES DIVISION 1701 NIMBUS ROAD RANCHO CORDOVA, CA 95701 UNDER CONTRACT NUMBER 8023 1994 Jennings and Hayes: Species of Special Concern i Date of Submission: December 8, 1993 Date of Publication: November 1, 1994 Jennings and Hayes: Species of Special Concern ii TABLE OF CONTENTS ABSTRACT . 1 PREFACE . 3 INTRODUCTION . 4 METHODS . 5 RESULTS . 11 CALIFORNIA TIGER SALAMANDER . 12 INYO MOUNTAINS SALAMANDER . 16 RELICTUAL SLENDER SALAMANDER . 18 BRECKENRIDGE MOUNTAIN SLENDER SALAMANDER . 20 YELLOW-BLOTCHED SALAMANDER . 22 LARGE-BLOTCHED SALAMANDER . 26 MOUNT LYELL SALAMANDER . 28 OWENS VALLEY WEB-TOED SALAMANDER . 30 DEL NORTE SALAMANDER . 32 SOUTHERN SEEP SALAMANDER . 36 COAST RANGE NEWT . 40 TAILED FROG . 44 COLORADO RIVER TOAD . 48 YOSEMITE TOAD . 50 ARROYO TOAD . 54 NORTHERN RED-LEGGED FROG . 58 CALIFORNIA RED-LEGGED FROG . 62 FOOTHILL YELLOW-LEGGED FROG .
    [Show full text]
  • California Wildlife Habitat Relationships System California Department of Fish and Game California Interagency Wildlife Task Group
    California Wildlife Habitat Relationships System California Department of Fish and Game California Interagency Wildlife Task Group Western Aquatic Garter Snake Thamnophis couchii R063 Winter Range Summer Range Yearlong Range County Boundaries Water Bodies Original Map: J Vindum (1999) Revision History: 0 25 50 100 Miles Range maps are based on available occurrence data and professional knowledge. They represent current, but not historic or potential, range. Unless otherwise noted above, maps were originally published in Zeiner, D.C., W.F. Laudenslayer, Jr., K.E. Mayer, and M. White, eds. 1988-1990. California's Wildlife. Vol. I-III. California Depart. of Fish and Game, Sacramento, California. Updates are noted in maps that have been added or edited since original publication. California Wildlife Habitat Relationships System California Department of Fish and Game California Interagency Wildlife Task Group WESTERN AQUATIC GARTER SNAKE Thamnophis couchii Family: NATRICIDAE Order: SQUAMATA Class: REPTILIA R063 Written by: T. Kucera, 1997 Updated by: CWHR Staff, February 2008 DISTRIBUTION, ABUNDANCE, AND SEASONALITY The Western aquatic garter snake occurs in the western Sierra Nevada from the Pit and Sacramento rivers south to the western end of the Tehachapi Mountains, and also in the Owens Valley (Rossman et al. 1996). Elevations range to about 2,438 m (7,500 ft) (Stebbins 1985). Rossman and Stewart (1987) demonstrated that T. couchii is a species distinct from T. atratus, T. gigas, and T. hammondii. Associated with permanent or semi-permanent bodies of water, especially rocky creeks, from slow-moving, low-elevation seasonal creeks to high-elevation mountain streams, ponds, and lakes in a variety of habitats including Montane Riparian, Montane Hardwood Conifer, Montane Chaparral, and Sierran Mixed Conifer (Rossman et al.
    [Show full text]
  • 3.4 Biological Resources for the Purpose of This EIR, Biological Resources Comprise Vegetation, Wildlife, Natural Communities, and Wetlands and Other Waters
    Impact Analysis Alameda County Community Development Agency Biological Resources 3.4 Biological Resources For the purpose of this EIR, biological resources comprise vegetation, wildlife, natural communities, and wetlands and other waters. Potential biological resource impacts associated with the program and the two individual projects are analyzed. Potential impacts are described quantitatively and qualitatively in Section 3.4.2, Environmental Impacts. This section also identifies specific and detailed measures to avoid, minimize, or compensate for potentially significant impacts on biological resources, where necessary. 3.4.1 Existing Conditions Regulatory Setting Federal Endangered Species Act Pursuant to the federal Endangered Species Act (ESA), USFWS and the National Marine Fisheries Service (NMFS) have authority over projects that may result in take of a species listed as threatened or endangered under the act. Take is defined under the ESA, in part, as killing, harming, or harassing. Under federal regulations, take is further defined to include habitat modification or degradation that results, or is reasonably expected to result, in death or injury to wildlife by significantly impairing essential behavioral patterns, including breeding, feeding, or sheltering. If a likelihood exists that a project would result in take of a federally listed species, either an incidental take permit, under Section 10(a) of the ESA, or a federal interagency consultation, under Section 7 of the ESA, is required. Several federally listed species—vernal pool fairy shrimp (Branchinecta lynchi), longhorn fairy shrimp (Branchinecta longiantenna), vernal pool tadpole shrimp (Lepidurus packardi), California tiger salamander (Ambystoma californiense), California red‐legged frog (Rana draytonii), Alameda whipsnake (Masticophis lateralis euryxanthus), and San Joaquin kit fox (Vulpes macrotis mutica)—have the potential to be affected by activities associated with the Golden Hills and Patterson Pass projects as well as subsequent repowering projects.
    [Show full text]