Here Describe This Pattern of Absence and Lay out a Plan for Restoring the Species to Areas Where the Species Has Recently Gone Extinct
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Noble et al. GigaScience (2016) 5:40 DOI 10.1186/s13742-016-0145-2 DATA NOTE Open Access A picture is worth a thousand data points: an imagery dataset of paired shrub-open microsites within the Carrizo Plain National Monument Taylor J. Noble1*, Christopher J. Lortie1, Michael Westphal2 and H. Scott Butterfield3 Abstract Background: Carrizo Plain National Monument (San Joaquin Desert, California, USA) is home to many threatened and endangered species including the blunt-nosed leopard lizard (Gambelia sila). Vegetation is dominated by annual grasses, and shrubs such as Mormon tea (Ephedra californica), which is of relevance to our target species, the federally listed blunt-nosed leopard lizard, and likely also provides key ecosystem services. We used relatively nonintrusive camera traps, or trail cameras, to capture interactions between animals and these shrubs using a paired shrub-open deployment. Cameras were placed within the shrub understory and in open microhabitats at ground level to estimate animal activity and determine species presence. Findings: Twenty cameras were deployed from April 1st, 2015 to July 5th, 2015 at paired shrub-open microsites at three locations. Over 425,000 pictures were taken during this time, of which 0.4 % detected mammals, birds, insects, and reptiles including the blunt-nosed leopard lizard. Trigger rate was very high on the medium sensitivity camera setting in this desert ecosystem, and rates did not differ between microsites. Conclusions: Camera traps are an effective, less invasive survey method for collecting data on the presence or absence of desert animals in shrub and open microhabitats. A more extensive array of cameras within an arid region would thus be an effective tool to estimate the presence of desert animals and potentially detect habitat use patterns. -
Target Species Mapping for the Green Visions Plan
Target Species Habitat Mapping California Quail and Mountain Quail (Callipepla californica and Oreortyx pictus) Family: Phasianidae Order: Galliformes Class: Aves WHR #: B140 and B141 Distribution: California quail are found in southern Oregon, northern Nevada, California, and Baja California, and have been introduced in other states such as Hawaii, Washington, Idaho, Colorado, and Utah (Peterson 1961). In California, they are widespread but absent from the higher elevations of the Sierra Nevada, the Cascades, the White Mountains, and the Warner Mountains, and are replaced by the related Gambel’s quail (C. gambelii) in some desert regions (Peterson 1961, Small 1994). In southern California, they are found from the Coast Range south to the Mexican border, and occur as far east as the western fringes of the Mojave and Sonoran deserts, such as in the Antelope Valley (Garrett and Dunn 1981, Small 1994). California quail range from sea level to about 5000 ft (1524 meters; Stephenson and Calcarone 1999) Mountain quail are resident from northern Washington and northern Idaho, south through parts of Oregon, northwestern Nevada, California, and northern Baja California (Peterson 1961). In southern California, mountain quail are found in nearly all of the mountain ranges west of the deserts, including the southern Coast Ranges, from the Santa Lucia Mountains south through Santa Barbara and Ventura counties, and the Peninsular Ranges south to the Mexican border (Garrot and Dunn 1981, Small 1994). In the Transverse Ranges, a small population occurs in the western Santa Monica Mountains, and larger populations occur in the San Gabriel and San Bernardino Mountains (Small 1994). Mountain quail are found at elevations from below 2000 ft (610 meters) to over 9000 ft (2743 meters; Stephenson and Calcarone 1999). -
Mckittrick Elementary School Relocation
Reconnaissance Level Biological Evaluation For APN 497-010-94 Section 20, T30S, R27E, MDB&M Bakersfield, California October 2019 Prepared for: The Nicholson Group 2101 San Gabriel Avenue Clovis, California 93611 Prepared by: _________________________________ Steven P. Pruett, Senior Biologist McCormick Biological, Inc. P.O. Box 80983 Bakersfield, California 93380 Table of Contents EXECUTIVE SUMMARY ............................................................................................................. 4 1.0 INTRODUCTION ..................................................................................................................... 4 1.1 Purpose and Background ................................................................................................... 4 1.2 Project Site and Surrounding Area Descriptions............................................................... 5 1.3.2 Migratory Bird Treaty Act ......................................................................................... 6 1.3.3 California Fish and Game Code (C.F.G.C. § 1580 et seq.) ....................................... 6 2.0 METHODS .............................................................................................................................. 12 3.0 RESULTS ................................................................................................................................ 14 3.1 General Conditions .......................................................................................................... 14 3.2 Special-status -
PREDATION of the ENDANGERED BLUNT-NOSED LEOPARD LIZARD (GAMBELIA SILA) in the SAN JOAQUIN DESERT of CALIFORNIA Author: David J
PREDATION OF THE ENDANGERED BLUNT-NOSED LEOPARD LIZARD (GAMBELIA SILA) IN THE SAN JOAQUIN DESERT OF CALIFORNIA Author: David J. Germano Source: The Southwestern Naturalist, 63(4) : 276-280 Published By: Southwestern Association of Naturalists URL: https://doi.org/10.1894/0038-4909-63-4-276 BioOne Complete (complete.BioOne.org) is a full-text database of 200 subscribed and open-access titles in the biological, ecological, and environmental sciences published by nonprofit societies, associations, museums, institutions, and presses. Your use of this PDF, the BioOne Complete website, and all posted and associated content indicates your acceptance of BioOne’s Terms of Use, available at www.bioone.org/terms-of-use. Usage of BioOne Complete content is strictly limited to personal, educational, and non-commercial use. Commercial inquiries or rights and permissions requests should be directed to the individual publisher as copyright holder. BioOne sees sustainable scholarly publishing as an inherently collaborative enterprise connecting authors, nonprofit publishers, academic institutions, research libraries, and research funders in the common goal of maximizing access to critical research. Downloaded From: https://bioone.org/journals/The-Southwestern-Naturalist on 22 Oct 2019 Terms of Use: https://bioone.org/terms-of-use Access provided by Southwestern Association of Naturalists THE SOUTHWESTERN NATURALIST 63(4): 276–280 PREDATION OF THE ENDANGERED BLUNT-NOSED LEOPARD LIZARD (GAMBELIA SILA) IN THE SAN JOAQUIN DESERT OF CALIFORNIA DAVID J. GERMANO Department of Biology, California State University, Bakersfield, CA 93311-1099 Correspondent: [email protected] ABSTRACT—Predation can significantly affect prey populations, which could be significant for recovering species threatened with extinction. -
Gambelia Sila) Including Another by the Long-Nosed Snake (Rhinocheilus Lecontei)
Western Wildlife 2:44–45 • 2015 Submitted: 20 November 2015; Accepted 22 November 2015. Peer Edited Notes Predation Events on the Endangered Blunt-nosed Leopard Lizard (Gambelia sila) Including Another by the Long-nosed Snake (Rhinocheilus lecontei) David J. Germano1,4, Erin N. Tennant2, and Lawrence R. Saslaw3 1Department of Biology, California State University, Bakersfield, California 93311-1022 2California Department of Fish and Wildlife, 1234 E. Shaw Avenue, Fresno, CA 93710 314700 Orchard Crest Avenue, Bakersfield, California 93314 4Corresponding author, e-mail: [email protected] Abstract.—In our initial report of predation of a Blunt-nosed Leopard lizard (Gambelia sila) by a Long-nosed Snake (Rhi- nocheilus lecontei), we speculated that the snake was not an important source of predation on this endangered lizard. Here we report a second instance of predation by the Long-nosed Snake and reassess its impact on Blunt-nosed Leopard Lizards. We also report other suspected predation events on Blunt-nosed Leopard Lizards by other predators that we found during radio-telemetry studies on the Lokern Natural Area, Semitropic Natural Area, and at Pixley National Wildlife Refuge in the San Joaquin Desert of California in 2015. Key Words.—birds; California; lizards; predators; Red-tailed Hawk; San Joaquin Desert; snakes Snakes are known predators of Blunt-nosed Leopard lizards (Gambelia sila) and recently we reported on an act of predation by a Long-nosed Snake (Rhinocheilus lecontei) at the Lokern Natural Area in Kern County, California (Germano and Saslaw 2015). Because of the small size of Long-nosed Snakes compared to leopard lizard adults and the relative scarcity of the snake in the San Joaquin Desert, we speculated that this snake likely was not an important source of predation on the endan- gered leopard lizard (Germano and Saslaw 2015). -
Habitat Use and Home Range of Long-Nosed Leopard Lizards (Gambelia Wislizenii) in Canyons of the Ancients National Monument, Colorado
Herpetological Conservation and Biology 6(2):312–323. Submitted: 2 March 2011; Accepted: 14 July 2011. HABITAT USE AND HOME RANGE OF LONG-NOSED LEOPARD LIZARDS (GAMBELIA WISLIZENII) IN CANYONS OF THE ANCIENTS NATIONAL MONUMENT, COLORADO 1,3 1 2 ROBERT A. SCHORR , BRAD A. LAMBERT , AND ERIC FREELS 1Colorado Natural Heritage Program, Colorado State University, Fort Collins, Colorado 80523, USA 2Dolores Public Lands Office, San Juan Public Lands, 100 North Sixth Street, Box 210, Dolores, Colorado 81323, USA 3Corresponding author, e-mail: [email protected] Abstract.—An understanding of species’ habitat requirements is needed for effective land management decisions, but for many North American reptiles, habitat use information is lacking. Gambelia wislizenii (Long-nosed Leopard Lizard) is a predatory lizard of most North American deserts, and, although common in the interior of its range, appears to be declining at some peripheral populations. To understand habitat use and movement patterns, we used telemetry and two habitat comparison methods to study a G. wislizenii population at the eastern boundary of the range. Gambelia wislizenii home ranges at Canyons of the Ancients National Monument, Colorado, are the largest recorded. Habitat analysis using microsite-attribute comparisons and compositional analysis documented second-order habitat preference for Big Sagebrush- or Utah Juniper-dominated landscapes. Gambelia wislizenii were found in areas with moderate shrub and forb cover with much bare ground, but were not found in areas dominated with grass cover. Incorporating management strategies that limit grass encroachment and maintain bare ground cover with moderate tree and shrub cover may help sustain G. wislizenii populations. -
Habitat Restoration Opportunities, Climatic Niche Contraction, and Conservation Biogeography in California's San Joaquin Desert
Habitat restoration opportunities, climatic niche contraction, and conservation biogeography in California's San Joaquin Desert Running head: Habitat restoration opportunities and climatic niche contraction in California's San Joaquin Desert Joseph A E Stewart1,2*, H Scott Butterfield3, Jonathan Q Richmond4, David J Germano5, Michael F Westphal6, Erin N Tennant7, Barry Sinervo1,2 1 Department of Ecology and Evolutionary Biology, University of California Santa Cruz, 1156 High St, Santa Cruz, CA 95064, USA. 2 Institute for the Study of Ecological and Evolutionary Climate Impacts, University of California, 100 Shaffer Road, Santa Cruz, CA 95060, USA. 3 The Nature Conservancy, 201 Mission St, San Francisco, CA, 94105, USA. 4 U.S. Geological Survey, 4165 Spruance Rd., Suite 200, San Diego, CA, 92101, USA. 5 Department of Biology, California State University Bakersfield, 9001 Stockdale Hwy, Bakersfield, CA, 93311, USA. 6 U.S. Bureau of Land Management, 940 2nd Ave., Marina, CA, 93933, USA. 7 Lands Unit, Central Region, California Department of Fish and Wildlife, 1234 E. Shaw Ave., Fresno, CA, 93710, USA. * To whom correspondence may be addressed. E-mail: [email protected] 1 PeerJ Preprints | https://doi.org/10.7287/peerj.preprints.26758v2 | CC0 Open Access | rec: 10 Jan 2019, publ: 10 Jan 2019 Abstract A recent global trend toward retirement of farmland presents opportunities to reclaim habitat for threatened and endangered species. We examine habitat restoration opportunities in one of the world’s most converted landscapes, California’s San Joaquin Desert (SJD). Despite the presence of 35 threatened and endangered species, agricultural expansion continues to drive habitat loss in the SJD, even as marginal farmland is retired. -
California Wildlife Habitat Relationships System California Department of Fish and Wildlife California Interagency Wildlife Task Group
California Wildlife Habitat Relationships System California Department of Fish and Wildlife California Interagency Wildlife Task Group SIERRA NEWT Taricha sierrae Family: SALAMANDRIDAE Order: CAUDATA Class: AMPHIBIA A075 Written by: S. Morey Reviewed by: T. Papenfuss Updated by: CWHR Staff May 2013 and Dec 2018 DISTRIBUTION, ABUNDANCE, AND SEASONALITY The Sierra newt is found the length of the Sierra, primarily in the foothills; an isolated population also occurs near the headwaters of Shasta Reservoir in Shasta Co. A few populations are also known from the floor of the Central Valley. Occurs primarily in valley- foothill hardwood, valley-foothill hardwood-conifer, coastal scrub and mixed chaparral, but is also known from annual grassland and mixed conifer types. Elevation range extends from near sea level to about 1830 m (6000 ft) (Jennings and Hayes 1994). SPECIFIC HABITAT REQUIREMENTS Feeding: Postmetamorphic juveniles and terrestrial adults take earthworms, snails, slugs, sowbugs, and insects (Stebbins 1972). Adult males at breeding ponds have been shown to take the eggs and hatching larvae of their own species (Kaplan and Sherman 1980) late in the breeding season, the eggs of other amphibians and trout, as well as adult and larval aquatic insects, small crustaceans, snails, and clams (Borell 1935). Aquatic larvae eat many small aquatic organisms, especially crustaceans. Cover: Terrestrial individuals seek cover under surface objects such as rocks and logs, within hollowed out trees, or in mammal burrows, rock fissures, or human-made structures such as wells. Aquatic larvae find cover beneath submerged rocks, logs, debris, and undercut banks. Reproduction: Eggs are laid in small firm clusters on the submerged portion of emergent vegetation, on submerged vegetation, rootwads, unattached sticks, and on the underside of cobbles off the bottom. -
A Co-Evolutionary Arms Race: Sierra Garter Snake Vs. Sierra Newt by Denise De Carion
FLOG A Co-Evolutionary Arms Race: Sierra garter snake vs. Sierra newt By Denise De Carion Photo credits: Patrick Hilton (left) and Denise De Carion (right). In the Tuolumne River watershed, there is a co-evolutionary arms race occurring between the Sierra garter snake (Thamnophis couchii) and the Sierra newt (Taricha sierrae) and it has become apparent that the Sierra garter snake is winning. The Sierra newt is an amphibious species whose conspicuous orange coloration provides a warning signal to predators (Petranka, 1998). This animal produces a potent neurotoxin called tetrodotoxin, which if ingested, binds to sodium ion channels in nerves and muscles, causing imminent mortality (Brodie, 2005). It is this molecular mechanism that allows the newt, which is slow-moving and often found out in exposed, shallow pool habitat, to avoid predation by almost all animals occupying higher trophic levels ―except for one. The Sierra garter snake has evolved an elevated resistance to tetrodotoxin, which prevents the toxin from binding to its pores. The deadly toxin is considered to be the phenotypic interface of interactions between these two species that has allowed them to co-evolve via natural selection. In other words, this example of a parallel “arms race” between predator and prey demonstrates that co-evolution of two species surrounding a toxin has been a result of each species having the genetic ability to respond and reciprocate to selection (Brodie et al., 2005). If you are planning to go ‘herping,’ or searching for reptiles and amphibians, on the Tuolumne River, the following words of advice should be followed. -
1 2 Habitat Restoration Opportunities, Climatic Niche Contraction, and Conservation Biog
1 Supplementary online information for: 2 3 Habitat restoration opportunities, climatic niche contraction, and conservation biogeography 4 in California's San Joaquin Desert 5 6 Joseph A E Stewart, H Scott Butterfield, Jonathan Q Richmond, David J Germano, Michael F 7 Westphal, Erin N Tennant, Barry Sinervo 8 9 Appendix S1. Discussion of potential impact of climate change. 10 Much uncertainty remains in how blunt-nosed leopard lizards (Gambelia sila) will 11 respond to climate change. Given uncertainty in the impacts of climate change, the ideal 12 conservation strategy may be functionally equivalent to the ideal conservation strategy in the 13 absence of climate change: managers should maintain a diverse portfolio of genetic lineages on 14 environmentally diverse habitats (Lawler, 2009). 15 On the mesic margin of the species’ distribution, historical and modern distributional 16 limits appear to be governed by herbaceous vegetation productivity (i.e. AET, Figure S2). This 17 limit to the species’ climatic niche is supported by multiple lines of evidence: demographic 18 decline in response to high precipitation years with high herbaceous biomass (Germano & 19 Williams, 2005), observations of G. sila having difficulty moving through dense thatch, the 20 apparent invasive-species-mediated climatic niche contraction we document in this paper 21 (Section 3.3) , and geographic patterns in occurrence data. Accordingly, our distribution models 22 are sensitive to changes in precipitation and evapotranspiration, with scenarios of decreased 23 future precipitation resulting in projections of peripheral range expansion and scenarios of 24 increased future precipitation resulting in projections of peripheral range contraction (Figure S4). 25 While the current distribution of G. -
Salamander Species Listed As Injurious Wildlife Under 50 CFR 16.14 Due to Risk of Salamander Chytrid Fungus Effective January 28, 2016
Salamander Species Listed as Injurious Wildlife Under 50 CFR 16.14 Due to Risk of Salamander Chytrid Fungus Effective January 28, 2016 Effective January 28, 2016, both importation into the United States and interstate transportation between States, the District of Columbia, the Commonwealth of Puerto Rico, or any territory or possession of the United States of any live or dead specimen, including parts, of these 20 genera of salamanders are prohibited, except by permit for zoological, educational, medical, or scientific purposes (in accordance with permit conditions) or by Federal agencies without a permit solely for their own use. This action is necessary to protect the interests of wildlife and wildlife resources from the introduction, establishment, and spread of the chytrid fungus Batrachochytrium salamandrivorans into ecosystems of the United States. The listing includes all species in these 20 genera: Chioglossa, Cynops, Euproctus, Hydromantes, Hynobius, Ichthyosaura, Lissotriton, Neurergus, Notophthalmus, Onychodactylus, Paramesotriton, Plethodon, Pleurodeles, Salamandra, Salamandrella, Salamandrina, Siren, Taricha, Triturus, and Tylototriton The species are: (1) Chioglossa lusitanica (golden striped salamander). (2) Cynops chenggongensis (Chenggong fire-bellied newt). (3) Cynops cyanurus (blue-tailed fire-bellied newt). (4) Cynops ensicauda (sword-tailed newt). (5) Cynops fudingensis (Fuding fire-bellied newt). (6) Cynops glaucus (bluish grey newt, Huilan Rongyuan). (7) Cynops orientalis (Oriental fire belly newt, Oriental fire-bellied newt). (8) Cynops orphicus (no common name). (9) Cynops pyrrhogaster (Japanese newt, Japanese fire-bellied newt). (10) Cynops wolterstorffi (Kunming Lake newt). (11) Euproctus montanus (Corsican brook salamander). (12) Euproctus platycephalus (Sardinian brook salamander). (13) Hydromantes ambrosii (Ambrosi salamander). (14) Hydromantes brunus (limestone salamander). (15) Hydromantes flavus (Mount Albo cave salamander). -
Amphibian Watch 2018 ELDORADO NATIONAL FOREST
Amphibian Watch 2018 ELDORADO NATIONAL FOREST PRESENTED BY HEATHER PERRY, PhD A Few Rules No handling of amphibians or reptiles under any circumstance Health and Safety of animals & humans No harassing of amphibians Especially during breeding No sharing of data Amphibian Morphology IN ALL THINGS OF NATURE THERE IS SOMETHING OF THE MARVELOUS ~ARISTOTLE Frogs and Toads Smooth skin Dry skin & warts/bumps Often reside near aquatic Parotoid glands that produce environments as adults defensive secretions, located behind eye Egg masses in clumps Migrate between terrestrial & aquatic ecosystems during breeding season Eggs laid in strings External Morphology Breeding & Egg Masses Toads in amplexus; eggs laid in string formation Frogs in amplexus; eggs laid in clumps/masses Amplexus: the mating method in frogs and toads where the male clasps the female about the back. Eggs are fertilized externally. Females are often larger than males. Salamanders and Newts Photo G. Nafis Rough-skinned when in the Well developed toes for digging terrestrial phase Long, rounded tails Aquatic during breeding Smooth skin season Paddle-like tail Breeding and Egg Masses Sierra Newts are more commonly encountered during mating season. They return to aquatic systems and can be seen in amplexus or mating balls. Eggs are laid and attached to submerged substrates. Long toed salamander eggs attached to submerged woody debris. Photos G. Nafis Tadpole vs. Larvae Tadpoles Larvae • Generally no external gills • External gills • Hind legs develop first • Forelegs develop first • Head is globular • Body is generally more slender Frogs & Toads THREATENED & ENDANGERED Sierra Nevada Yellow-legged Frog Distribution (Rana sierrae) High elevation species (ENDEMIC) Status: Endangered Declines are attributed to: pesticides, chytridiomycosus, and fish introductions Highly sensitive to climate change due to changes in wildfire and hydrologic regimes Audio by G.