About Nature: Amphibians and Reptiles
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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. -
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). -
91 Table F-10 Golden Eagle REA Mitigation
91 Table F-10 Golden Eagle REA Mitigation: Extrapolation of the Relative Productivity of Electric Pole Retrofitting in 2011 Over the 30 Years Associated with the Average Life Cycle of Wind Energy Projects Table F-11 Golden Eagle REA Scaling: Mitigation Owed for a 5-Year Permitted Take of 25 Golden Eagles (5 Eagles Annually) (REA Step 16) Total Debit 485.74 PV bird-years for 5 years of Golden Eagle take ÷ Relative Productivity of Electric Pole Retrofitting ÷4.20 Avoided loss of PV bird-years per retrofitted pole = Mitigation owed =115.61 Poles to be retrofitted to achieve no net loss PV=Present Value 92 APPENDIX G COMPENSATORY MITIGATION CASE STUDY7: POWER POLE RETROFITTING TO COMPENSATE FOR TAKE OF GOLDEN EAGLES To offset projected and permitted take, retrofitting of non- Avian Power Line Interaction Committee (APLIC) compliant power poles has been selected by the Service as the initial focus of compensatory mitigation projects. Raptor electrocution is a known source of eagle mortality in the United States (Franson et al. 1995, Millsap et al. 2004, APLIC 2006, Lehman et al. 2007, Lehman et al. 2010). In particular, Golden Eagles are electrocuted more than any other raptor in North America; Lehman et al. (2007) noted Golden Eagles accounted for 50 – 93% of all reported mortalities of raptor electrocutions. Eagles often come into contact with non-APLIC compliant electric transmission poles. These poles are often responsible for the high incidence of eagle mortality, especially in open habitat devoid of natural perches. Specific utility poles and line spans in need of retrofit due to known mortalities of eagles and other large raptors will be reviewed by the Service and selected for retrofit based on criteria specified below. -
Schall and Dearing.Pdf
Oecologia (Berlin) (1987) 73:389-392 LxA70u c Springer-Verlag 1987 Malarial parasitism and male competition for mates in the western fence lizard, Sceloporus occidentalis J.J. Schall and M.D. Dearing Department of Zoology, University of Vermont, Burlington, VT 05405, USA Summary. The effect of malarial parasitism on the ability the outcome of male-male interactions and female choice of male western fence lizards, Sceloporus occidentalis, to in the western fence lizard, Sceloporusoccidentalis, in Cali- compete for access to females was assessed experimentally. fornia, USA. The mating system of S. occidentalisis polyga- Pairs of male lizards, one infected with the malarial para- mous. Males interact agonistically toward other males and site, Plasmodium mexicanum, and the other not infected, vigorously court females during the reproductive season. were matched by size and color and placed in large semina- Their conspicuous stereotyped behaviors include bobbing, tural outdoor enclosures along with an adult female lizard. shaking, and display of brightly colored ventral color Infected males displayed to females and to other males less patches (Schall and Sarni 1987; Ressel 1986). At our study often than did noninfected male lizards. Noninfected lizards site approximately 25% of adult male fence lizards are in- were dominant in social interactionsmore often than malar- fected with the malarial parasite, Plasmodiummexicanum ious animals, based on duration and intensity of agonistic (Schall 1983; Bromwich and Schall 1986). This parasite re- encounters toward the other male, and time spent with the duces the ability of the fence lizard to engage in intense female. Thus, malarial infection hinders the ability of male activity; infected males also have smaller testes (Schall fence lizards to compete for mates. -
EUROPEAN WALL LIZARDS (Podarcis Muralis)
INVASIVE SPECIES ALERT! EUROPEAN WALL LIZARDS (Podarcis muralis) NATIVE RANGE European Wall Lizards are native to southern Belgium and Germany, south to northern Spain, and east to Turkey. The European Wall Lizards in B.C. are thought to be native to Italy. DESCRIPTION European Wall Lizards... Have a long, slender, flattened body Photo: Gavin Hanke Can grow to be 63 mm in length (snout to base of tail) Can have a tail 1.5 times the length of body Have small, bead-like scales on back and sides PRIMARY IMPACT: Have 6 rows of large rectangular scales on belly region Have long fingers and toes European Wall Do not have skin folds on back and sides of body Lizards may impact Are variable in colour, ranging from brown to grey to green May have black-blue spots on the flank (especially males) native species Adults usually have prominent flecks of green on the back, intensely through competition coloured over the shoulders and predation. WHY SHOULD WE CARE? European Wall Lizards... Can gather in large densities, which can potentially impact native DID YOU KNOW? species and ecosystems that are not adapted to their presence If a European Wall Lizard is Could compete for food and shelter with B.C.’s native Northern captured, it will drop its tail to Alligator Lizard (Elgaria coerulea) or endangered Sharp-Tailed Snake (Contia tenuis) escape. The tail keeps wiggling for a few minutes in order to LOOKALIKES distract the predator, giving European Wall Lizards can be confused with native Northern Alligator Lizards the lizard a chance to escape. -
Fluorescence Emission in a Marine Snake
Galaxea, Journal of Coral Reef Studies 21: 7-8(2019) Photogallery Fluorescence emission in a marine snake Takashi SEIKO and Yohey TERAI SOKENDAI (The Graduate University for Advanced Studies), Department of Evolutionary Studies of Biosystems, Shonan Village, Hayama, Kanagawa 240-0193, Japan. Corresponding authors: Y. Terai, T. Seiko Emails: [email protected]; [email protected] Communicated by Frederic Sinniger (Associate EditorsinChief) Keywords fluorescence, Laticauda, marine reptile, sea krait Coral reefs are one of the most colorful environments on Earth. Light in coral reefs includes fluorescence as well as reflectance of sunlight. In fluorescence, mole cules are excited by illuminating light and emit longer wavelength fluorescence than the excitation light wave length. In coral reefs, fluorescent light emission is observed in a range of taxa including cnidarians (e.g. corals), arthropods and fishes (e.g., Johnsen 2012). In marine reptiles, fluorescent emission has reported thus far only from sea turtles (Gruber and Sparks 2015). Here we report fluorescent light emission in a marine snake. Laticauda laticaudata Linnaeus, 1758 is a semi aquatic sea krait (Elapidae: Laticaudinae) often ob served in coral reefs. We examined a specimen that was freshly frozen after death and subsequently thawed. This speci men was caught at Oganzaki, Ishigaki island, Oki nawa, Japan (24°27′12.4″N; 124°04′37.4″E) Fig. 1 Photographs of a sea krait (Laticauda laticaudata) illuminated with white light (A) without a filter, and ultraviolet LED light (B) through a blue light cutting filter (<490 nm). (C) A reflectance and fluorescence light spectrum measured from a pale band. -
Northern Alligator Lizard Elgaria Coerulea (Weigmann,1828) Natural History Summary by Kate Durost
NORTHERN ALLIGATOR LIZARD ELGARIA COERULEA (WEIGMANN,1828) NATURAL HISTORY SUMMARY BY KATE DUROST Classification Kingdom: Animalia Phylum: Chordata Class: Reptilia Order: Squamata Family: Anguidae Genus: Elgaria Species: E. coerulea Description The Northern Alligator Lizard (Elgaria coerulea) ranges in color from gray, olive, and rust, to greenish or bluish dorsally with heavy blotching or barring in a dusky color. Its eyes are completely dark or dark around the pupils. There are dark stripes between the scale rows on the belly, though they can sometimes be absent. Dorsal scales are usually in 16 rows. Four subspecies have been described: E. c. coerulea, E. c. shastensis, E. c. principis, and E. c. palmeri, with E. c. principis, or the Northwestern Alligator Lizard being the one most likely to be found in Washington. The Northwestern Alligator Lizard tends to be small – less than 4 in long, with a broad dorsal stripe of tan, olive, golden brown, or gray and contrasting dusky sides. The dorsal scales are weakly keeled in 14 rows with the temporal scales also being weakly keeled (Stebbins 2003). Distribution The Northern Alligator Lizard is found along the western coast of North America. Elgaria coeruela principis has the largest range of any of the subspecies, ranging from southern Oregon to British Columbia, Canada while the others are concentrated in California (CaliforniaHerps 2017). Elgaria coerulea’s range map is available at Hammerson 2007. Diet The Northern Alligator Lizard primarily eats a variety of small invertebrates like ticks, spiders, centipedes, slugs, millipedes, snails, and worms as well as any of their larvae. It will also eat small lizards and small mammals and occasionally feed on bird eggs and young birds (CaliforniaHerps, 2017; Stebbins 2003). -
Biological Opinion (Opinion) in Accordance with Section 7 of the Endangered Species Act of 1973 (Act), As Amended (16 U.S.C
In Reply Refer to: FWS-SDG-15B0072-20F1452 November 17, 2020 Sent Electronically Memorandum To: Regional Endangered Species Program Manager Sacramento, California From: Field Supervisor, Carlsbad Fish and Wildlife Office Carlsbad, California Subject: Intra-Service Formal Section 7 Consultation for the Issuance of an Amendment to the County of San Diego’s Endangered Species Act Section 10(a)(1)(B) Permit (PRT-840414) for the Multiple Species Conservation Program, San Diego Subarea Plan to address the Otay Ranch Village 14 and Planning Areas 16 and 19, San Diego County, California This document transmits the U. S. Fish and Wildlife Service’s (Service) biological opinion (Opinion) in accordance with section 7 of the Endangered Species Act of 1973 (Act), as amended (16 U.S.C. 1531 et seq.), regarding the issuance of an amendment to the incidental take permit (ITP) for the Multiple Species Conservation Program (MSCP) County of San Diego (County) Subarea Plan (Subarea Plan) for Otay Ranch Village 14 and Planning Areas 16 and 19 (Project) pursuant to section 10(a)(1)(B) of the Act. The Service issued the Section 10(a)(1)(B) permit (PRT-840414) to the County for their Subarea Plan on March 17, 1998. The permit duration is for 50 years. The County is requesting the Amendment to change the footprint of the Project, as well as add incidental take coverage for the federally endangered Quino checkerspot butterfly (Euphydryas editha quino; QCB) and San Diego fairy shrimp (Branchinecta sandiegonensis; SDFS). The MSCP is a comprehensive, 50-year habitat conservation plan program that addresses urban development and the needs of 85 covered species and the preservation of natural vegetation communities within a 582,243-acre planning area in southwest San Diego County (City of San Diego 1998). -
Greater Short-Horned Lizard (Phrynosoma Hernandesi) Is the Only Species of Lizard Found in Alberta and Saskatchewan
COSEWIC Assessment and Update Status Report on the Greater Short-horned Lizard Phrynosoma hernandesi in Canada ENDANGERED 2007 COSEWIC COSEPAC COMMITTEE ON THE STATUS OF COMITÉ SUR LA SITUATION ENDANGERED WILDLIFE DES ESPÈCES EN PÉRIL IN 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: COSEWIC 2007. COSEWIC assessment and update status report on the Greater Short-horned Lizard Phrynosoma hernandesi in Canada. Committee on the Status of Endangered Wildlife in Canada. Ottawa. vi + 41 pp. (www.sararegistry.gc.ca/status/status_e.cfm). Previous report: Powell, G. Lawrence and Russell, Anthony P. 1992. COSEWIC status report on the Greater Short- horned Lizard Phrynosoma hernandesi in Canada. Committee on the Status of Endangered Wildlife in Canada. Ottawa. 1-21 pp. Production note: COSEWIC would like to acknowledge Janice James for writing the status report on the Greater Short- horned Lizard Phrynosoma hernandesi in Canada, prepared under contract with Environment Canada, overseen and edited by Ron Brooks, Co-chair (Reptiles) of the COSEWIC Amphibians and Reptiles Species Specialist Subcommittee. For additional copies contact: COSEWIC Secretariat c/o Canadian Wildlife Service Environment Canada Ottawa, ON K1A 0H3 Tel.: 819-953-3215 Fax: 819-994-3684 E-mail: COSEWIC/[email protected] http://www.cosewic.gc.ca Également disponible en français sous le titre Ếvaluation et Rapport de situation du COSEPAC sur le grand iguane à petites cornes (Phrynosoma hernandesi) au Canada – Mise à jour. Cover illustration: Greater Short-horned Lizard — Provided by author. -
Biodiversity of Amphibians and Reptiles at the Camp Cady Wildlife
Ascending and descending limbs of hydrograph Pulse flow ascending-descending limbs of hydrograph Low Peak Restora- Low Peak Pulse Low release release tion release release restoration Shape release mag- Shape mag- release Shape mag- Date and Shape mag- release de- mag- Date and Water nitude ascend- nitude (hector descend- nitude duration flow Total Low ascend- nitude (hector scend- nitude duration flow to Total Year Year Flow (m3/s) ing (m3/s) m) ing (m3/s) to base-flow days (m3/s) ing (m3/s) m) ing (m3/s) base-flow days 25 Apr-22 1995 na Pre-ROD 14 R 131 na G 27 28 May 1996 na Pre-ROD 9 R 144 na G, 1B 14 10 May-9 Jun 31 1997 na Pre-ROD 10 R 62 na G, 3B 13 2 May-2 Jul 62 1998 na Pre-ROD 47 R 192 na G 13 24 May-27 Jul 65 1999 na Pre-ROD 15 G 71 na G 13 8 May-18 Jul 72 2000 na Pre-ROD 9 R 66 na G 13 8 May-27 Jul 81 2002 normal Pre-ROD 9 R 171 59,540 G 13 27 Apr-25 Jun 28 2003 wet Pulse 9 R 74 55,272 G, 2B 12 29 Apr-22 Jul 85 13 R 51 4,194 G 12 23 Aug-18 Sep 27 2004 wet Pulse 9 R 176 80,300 G, 4B 12 4 May-22 Jul 80 16 R 48 4,465 G 14 21 Aug-14 Sep 25 2005 wet ROD 8 R, 2 B 197 79,880 G, 1B 13 27 Apr-22 Jul 87 2006 extra wet ROD 8 G, 5B 286 99,900 G, 2B 13 16 Apr-22 Jul 98 2007 dry ROD 8 R 135 55,963 G 13 25 Apr-25 Jun 62 2008 dry ROD 9 R, 1B 183 80,016 G, 3B 20 22 Apr-15 Jul 85 2009 dry ROD 8 R 125 54,952 G, 4B 12 24 Apr-6 Jul 74 2010 wet ROD 9 R 194 81,003 G, 3B 12 22 Apr-2 Aug 102 2011 wet ROD 7 R, 2B 329 89,033 G, 2B 13 26 Apr-1 Aug 98 2012 normal Pulse 9 R, 2B 172 79,819 G, 4B 13 4 Apr-26 Jul 114 13 R, 1B 39 4,811 R, 1B 13 12 Aug-20 Sep -
Ventral Coloration and Body Condition Do Not Affect Territorial Behavior in Two Sceloporus Lizards
Ventral coloration and body condition do not affect territorial behavior in two Sceloporus lizards 1Marina Kelada, 1Courtney Moulton, 2Casey Nguyen, 3Griselda Robles Olague 1University of California, Riverside; 2University of California, Irvine; 3University of California, Santa Barbara Sceloporus lizards are known to be defensive of their territories, which provide shelter, food, water, and mates. They often exhibit territorial behavior through visual displays of aggression, specifically with pushups. Along with aggression, this display can also expose the blue coloration on their ventral side, serving as an intraspecific communication between lizards that reveals information about their dominance, sex, and species membership. In this study, we compared how blue coloration and body condition affected territorial behavior in two Sceloporus lizards: the well-studied western fence (Sceloporus occidentalis) and the understudied sagebrush (Sceloporus graciosus), two closely related lizards with overlapping ranges in the San Jacinto Mountains. We also addressed whether these species would exhibit character displacement in their ventral coloration as a result of their sympatry. ImageJ and Adobe Photoshop were used for photo analyses to quantify the proportion and intensity of blue on each lizard’s ventral side. Territoriality was measured through number of pushups displayed and distance traveled. We found that both ventral coloration and body condition had no effect on the territoriality of either species, suggesting that territorial behavior -
Proceedings of the United States National Museum
scripps institution FCR BIOLOGICAL RESEARCH SMITHSONIAN INSTITUTION. UNITED STATES NATIONAL MUSEUM. THB MAKiNE B>OLOCICAL A^0CIATI0N PROCEEDINGS OF TUB UNITED STATES NATIONAL MUSEUM. 3 I) -. Volume XIV 1891. PUBLISHED UNDER THE DIRECTION OF THE SMITHSONIAN INSTITUTION. WASHINGTON: '^ GOVERNMENT PRINTING OFFICE. 1892. NOTES ON SOME NORTH AMERICAN SNAKES. BY Leonhard Stejneger, Curator of the Department of Reptiles and Batrachians. ' Rena humilis B. & G. The Museum has recently received from Mr. Herbert Brown, Tucson, Arizona (who on several occasions has favored us with valuable mater ial), four specimens of this worm-snake, making the first record of this rare species from eastern Arizona. They are especially valuable because they show the individual variatiou both in the position of the eye and the width and shape of the median cephalic series of scales. We have now specimens from southern California, from Yuma, from Tucson, and from the Cape region of Lower California. Professor Cope has recorded it from Batopilas, Mexico (Proc. Amer. Philos. Soc, xvm, p. 262), though no reference to this locality is found in his Catalogue of Batrachians aud Reptiles of Central America and Mexico (Bull. U. S. Nat. Mus., No. 32, 1887).* It also occurs at Colima, on the west coast of Mexico, if I am not mistaken in referring Bocourt's Siagonodon dugesii (Miss. Sc. Mex., Kept., livr. 8, 1882, p. 507, pi. xxix, fig. 9, pi. xxx, fig. 4), as a synomym to the present species. I can find no character in the description, nor in the figures, by which to separate it from B. humilis. Leptotyphlopa dulcis (B.