AMPHIBIANS and REPTILES in Arizona
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Birds, Reptiles, Amphibians, Vascular Plants, and Habitat in the Gila River Riparian Zone in Southwestern New Mexico
Birds, Reptiles, Amphibians, Vascular Plants, and Habitat in the Gila River Riparian Zone in Southwestern New Mexico Kansas Biological Survey Report #151 Kelly Kindscher, Randy Jennings, William Norris, and Roland Shook September 8, 2008 Birds, Reptiles, Amphibians, Vascular Plants, and Habitat in the Gila River Riparian Zone in Southwestern New Mexico Cover Photo: The Gila River in New Mexico. Photo by Kelly Kindscher, September 2006. Kelly Kindscher, Associate Scientist, Kansas Biological Survey, University of Kansas, 2101 Constant Avenue, Lawrence, KS 66047, Email: [email protected] Randy Jennings, Professor, Department of Natural Sciences, Western New Mexico University, PO Box 680, 1000 W. College Ave., Silver City, NM 88062, Email: [email protected] William Norris, Associate Professor, Department of Natural Sciences, Western New Mexico University, PO Box 680, 1000 W. College Ave., Silver City, NM 88062, Email: [email protected] Roland Shook, Emeritus Professor, Biology, Department of Natural Sciences, Western New Mexico University, PO Box 680, 1000 W. College Ave., Silver City, NM 88062, Email: [email protected] Citation: Kindscher, K., R. Jennings, W. Norris, and R. Shook. Birds, Reptiles, Amphibians, Vascular Plants, and Habitat in the Gila River Riparian Zone in Southwestern New Mexico. Open-File Report No. 151. Kansas Biological Survey, Lawrence, KS. ii + 42 pp. Abstract During 2006 and 2007 our research crews collected data on plants, vegetation, birds, reptiles, and amphibians at 49 sites along the Gila River in southwest New Mexico from upstream of the Gila Cliff Dwellings on the Middle and West Forks of the Gila to sites below the town of Red Rock, New Mexico. -
Tantilla Hobartsmithi Taylor Smith's Black-Headed Snake
318.1 REPTILIA: SQUAMATA: SERPENTES: COLUBRIDAE TANTILLA HOBARTSMITHI Catalogue of American Amphibians and Reptiles. CHARLESJ. COLEANDLAURENCEM. HARDY. 1983. Tantilla hobartsmithi. Tantilla hobartsmithi Taylor Smith's black-headed snake Tantilla nigriceps (not of Kennicott): Van Denburgh and Slevin, 5MM 1913:423-424. ~ Tantilla planiceps (not of Blainville): Stejneger and Barbour, 1917: 105 (part). FIGURE2. Color pattern of head and neck of Tantilla hobart• Tantilla nigriceps eiseni (not of Stejneger): Woodbury, 1931:107• smithi, American Museum of Natural History 107377 (from Cole 108. and Hardy, 1981:210). Tantllla atriceps (not of Giinther): Taylor, "1936" [1937]:339-340 (part). Tantilla hobartsmithi Taylor, "1936" [1937]:340-342. Type-lo• in 1-3 rows (minimum) approximately encircling spinose midsec• cality, "near La Posa, 10 mi. northwest of Guaymas," So• tion of hemipenis; supralabials 7; infralabials 6; naris in upper nora, Mexico (Taylor, "1936" [1937]:340-341). The holotype, half of nasal; postoculars usually 2; temporals 1 + 1; mental usu• University of Illinois Museum of Natural History 25066, an ally touching anterior pair of genials. Most similar to T. atriceps; adult male (examined by authors), was collected by Edward differing strikingly in hemipenis" (Cole and Hardy, 1981:221). H. Taylor, the night of 3 July 1934. • DESCRIPTIONS. See Cole and Hardy (1981) for a redescrip• Tantilla utahensis Blanchard, 1938:372-373. Type-locality, "St. tion of the holotype (including description of hemipenis); general George, Washington County, Utah" (Blanchard, 1938:372). descriptions of size, coloration, hemipenes, scutellation, maxil• The holotype, California Academy of Sciences 55214, an adult lae, and chromosomes; and analyses of geographic variation. female (examined by authors), was collected by V. -
Appendix B References
Final Tier 1 Environmental Impact Statement and Preliminary Section 4(f) Evaluation Appendix B, References July 2021 Federal Aid No. 999-M(161)S ADOT Project No. 999 SW 0 M5180 01P I-11 Corridor Final Tier 1 EIS Appendix B, References 1 This page intentionally left blank. July 2021 Project No. M5180 01P / Federal Aid No. 999-M(161)S I-11 Corridor Final Tier 1 EIS Appendix B, References 1 ADEQ. 2002. Groundwater Protection in Arizona: An Assessment of Groundwater Quality and 2 the Effectiveness of Groundwater Programs A.R.S. §49-249. Arizona Department of 3 Environmental Quality. 4 ADEQ. 2008. Ambient Groundwater Quality of the Pinal Active Management Area: A 2005-2006 5 Baseline Study. Open File Report 08-01. Arizona Department of Environmental Quality Water 6 Quality Division, Phoenix, Arizona. June 2008. 7 https://legacy.azdeq.gov/environ/water/assessment/download/pinal_ofr.pdf. 8 ADEQ. 2011. Arizona State Implementation Plan: Regional Haze Under Section 308 of the 9 Federal Regional Haze Rule. Air Quality Division, Arizona Department of Environmental Quality, 10 Phoenix, Arizona. January 2011. https://www.resolutionmineeis.us/documents/adeq-sip- 11 regional-haze-2011. 12 ADEQ. 2013a. Ambient Groundwater Quality of the Upper Hassayampa Basin: A 2003-2009 13 Baseline Study. Open File Report 13-03, Phoenix: Water Quality Division. 14 https://legacy.azdeq.gov/environ/water/assessment/download/upper_hassayampa.pdf. 15 ADEQ. 2013b. Arizona Pollutant Discharge Elimination System Fact Sheet: Construction 16 General Permit for Stormwater Discharges Associated with Construction Activity. Arizona 17 Department of Environmental Quality. June 3, 2013. 18 https://static.azdeq.gov/permits/azpdes/cgp_fact_sheet_2013.pdf. -
Watchable Wildlife Form
U.S. Fish & Wildlife Service Watchable Wildlife Bitter Lake National Wildlife Refuge Welcome Roundnose minnow Dionda episcopa Amphibians Bitter Lake National Wildlife Refuge is one Speckled chub Extrarius aestivalis Family Ambystomatidae – Mole Salamanders of New Mexico’s most important sanctuaries Plains minnow Hybognathus placitus Tiger salamander Ambystoma tigrinum Arkansas River shiner Notropis girardi and breeding grounds for migratory birds and Family Leptodactylidae – Tropical Frogs Rio Grande shiner Notropis jemezanus other wildlife. Established in 1937, the 24,500- Eastern barking frog Eleutherodactylus augusti Pecos bluntnose shiner Notropis simus pecosensis acre refuge is strategically located along the latrans Pecos River where the Chihuahuan Desert Fathead minnow Pimephales promelas Family Pelobatidae – Spadefoot Toads meets the Great Plains. The convergence of Family Catostomidae – Suckers Couch’s spadefoot toad Scaphiopus couchii these vastly different terrains has produced a River carpsucker Carpoides carpio diverse range of habitats, providing a home to New Mexico spadefoot toad Spea multiplicata a rich array of plant and animal life, including Family Ictaluridae – Catfishes Plains spadefoot toad Spea bombifrons Channel catfish Ictalurus punctatus a number of rare species. Family Bufonidae – Toads Bitter Lake NWR is best known for its Family Cyprinodontidae – Pupfish Woodhouse’s toad Bufo woodhousii spectacular variety of birds, particularly the Pecos pupfish Cyprinodon pecosensis Red-spotted toad Bufo punctatus Great Plains toad Bufo cognatus large migrations of ducks, geese, and cranes Family Fundulidae – Killifishes Texas toad Bufo speciosus during the fall and winter months. Many of Plains killifish Fundulus zebrinus Western green toad Bufo debilis insidior these creatures are drawn by the refuge’s Rainwater killifish Lucania parva wetlands, which offer an abundance of food as Family Hylidae – Treefrogs Family Poeciliidae – Livebearers well as ideal nesting habitat for some species. -
University of Texas at Arlington Dissertation Template
EVOLUTIONARY RELATIONSHIPS IN SOME NORTHERN GROUPS OF THE DIRECT-DEVELOPING FROG GENUS CRAUGASTOR (ANURA: CRAUGASTORIDAE) by JEFFREY W. STREICHER Presented to the Faculty of the Graduate School of The University of Texas at Arlington in Partial Fulfillment of the Requirements for the Degree of DOCTOR OF PHILOSOPHY THE UNIVERSITY OF TEXAS AT ARLINGTON May 2012 Copyright © by Jeffrey W. Streicher 2012 All Rights Reserved ACKNOWLEDGEMENTS During my time at UT Arlington I have been assisted by an outstanding community of individuals. First, I thank my fellow graduate students who have not only challenged me to be a better biologist, but also provided friendship and moral support. I thank Jesse Meik, Christian Cox, Coleman Sheehy III, Thomas Eimermacher, Brian Fontenot, Walter Schargel, Andrea Acevedo, Corey Roelke, Mike Logan, Matt Ingrasci, Jacobo Reyes-Velasco, Ben Anders, Utpal Smart, David Sanchez, Paul Pasichnyk, Alex Hall, and Matt Watson. Second, I thank my committee members; Eric Smith, Jon Campbell, Paul Chippindale, Esther Betrán, and Jeff Demuth, for their support and advice. Third, I thank the administrative staff; Linda Taylor, Gloria Burlingham, and Peggy Fisher for always answering my questions. I thank the following individuals for field companionship during our U.S.A., Mexico, Ecuador, South Africa, Costa Rica, India, and Guatemala trips: Coleman Sheehy III, Christian Cox, Thomas Eimermacher, Beryl Wilson, Jesse Meik, Matt Ingrasci, Mario Yanez, Carlos Vásquez Almazán, Gustavo Ruano Fajardo, Jacobo Reyes-Velasco, Oscar Flores-Villela, Virginia León-Règagnon, Elizabeth Martínez- Salizar, Elisa Cabrera-Guzman, Ruben Tovar, Paulino Ponce-Campos, Toni Arizmendi- Espinosa, Carl Franklin, Eric Smith, Jonathan Campbell, Butch Brodie Jr., and Robert Makowsky. -
The San Pedro River in Southeastern Arizona
Lowland Riparian Herpetofaunas: The San Pedro River in Southeastern Arizona Philip C. Rosen School of Natural Resources, University of Arizona, Tucson, AZ Abstract—Previous work has shown that southeastern Arizona has a characteristic, high diversity lowland riparian herpetofauna with 62-68 or more species along major stream corridors, and 46-54 species in shorter reaches within single biomes, based on intensive fieldwork and museum record surveys. The San Pedro River supports this characteristic herpetofauna, at least some of which still occurs in the lower basin within the Sonoran Desert. It has about 64 species (55 vouchered to date), with 48-53 species within each of three somewhat ecologically homogeneous portions of the basin. This assemblage is more similar to other lowland herpetofaunas than to an example of a canyon riparian herpetofauna. Most of the characteristic riparian species are not known to be abundant along the San Pedro, and some expected species are apparently absent, suggesting that the herpetofauna may have not yet recovered from the history of grassland, cienega, and bottomland degradation. effort has been most focused in the upper basin, and it is dif- Introduction ficult to entirely separate riparian and non-riparian records, so Remarkably, the riparian herpetofauna of southeastern I have summarized the latter for the upper basin; in the lower Arizona has not been accurately described between Ruthven’s reaches, so little collecting has been done away from the river (1907) and Van Denburgh and Slevin’s (1913) annotations that this was not possible. Museum records were excluded if and records for the Santa Cruz River riparian at Tucson and localities could not be located to an adequate precision, but I the present. -
Year of the Snake News No
Year of the Snake News No. 6 June 2013 www.yearofthesnake.org Snakes of Narrow Habitats by Andrew M. Durso known! Known to the native people Thermophis baileyi, of Tibet for centuries, hot-spring one of two species of snakes were first discovered in 1907 Tibetan Hot-springs by Lieutenant F. Bailey, after whom Snake, the highest snake in the world, a one of the two species was named. In native of the Tibetan 2008 a second species of Thermophis Plateau. Photo by Kai was discovered and named Wang. Thermophis zhaoermii for preeminent Chinese herpetologist Zhao Ermi. One reason we know only a little about Thermophis is its high mountain habitat. Most of the Many snake species are habitat spending your whole life in one! mountain ranges in China run east- generalists, such as the familiar North Now imagine being the size of a west, but the Hengduan Mountains, American ratsnakes, Australian pencil and unable to regulate your where Hot-spring Snakes are found, tiger snakes, and European grass own body temperature, and you’re stretch north-south (the name snakes. However, some snakes are doing a pretty good approximation ‘‘Hengduan” means ‘‘to transect” so specialized, it’s hard to believe. of a Tibetan Hot-spring Snake and ‘‘cut downward” in Chinese). Here, I’ll profile a few of the most (Thermophis). These tiny snakes Parallel north-south sub-ranges of specialized snakes (in terms of reach only 2.5 feet (76 cm) in the Hengduans are separated by habitat) on Earth. length and are found at elevations deep river valleys through which flow the famous Three Parallel Hot-spring Snakes above 14,000 feet (4267 m) on the Tibetan plateau in south-central Rivers: the Nujiang (Salween), Everyone likes a good soak in a hot China, higher than any other snake Lantsang (Mekong), and Jinshajiang spring now and again, but imagine continued on p. -
Amphibians and Reptiles of the State of Coahuila, Mexico, with Comparison with Adjoining States
A peer-reviewed open-access journal ZooKeys 593: 117–137Amphibians (2016) and reptiles of the state of Coahuila, Mexico, with comparison... 117 doi: 10.3897/zookeys.593.8484 CHECKLIST http://zookeys.pensoft.net Launched to accelerate biodiversity research Amphibians and reptiles of the state of Coahuila, Mexico, with comparison with adjoining states Julio A. Lemos-Espinal1, Geoffrey R. Smith2 1 Laboratorio de Ecología-UBIPRO, FES Iztacala UNAM. Avenida los Barrios 1, Los Reyes Iztacala, Tlalnepantla, edo. de México, Mexico – 54090 2 Department of Biology, Denison University, Granville, OH, USA 43023 Corresponding author: Julio A. Lemos-Espinal ([email protected]) Academic editor: A. Herrel | Received 15 March 2016 | Accepted 25 April 2016 | Published 26 May 2016 http://zoobank.org/F70B9F37-0742-486F-9B87-F9E64F993E1E Citation: Lemos-Espinal JA, Smith GR (2016) Amphibians and reptiles of the state of Coahuila, Mexico, with comparison with adjoining statese. ZooKeys 593: 117–137. doi: 10.3897/zookeys.593.8484 Abstract We compiled a checklist of the amphibians and reptiles of the state of Coahuila, Mexico. The list com- prises 133 species (24 amphibians, 109 reptiles), representing 27 families (9 amphibians, 18 reptiles) and 65 genera (16 amphibians, 49 reptiles). Coahuila has a high richness of lizards in the genus Sceloporus. Coahuila has relatively few state endemics, but has several regional endemics. Overlap in the herpetofauna of Coahuila and bordering states is fairly extensive. Of the 132 species of native amphibians and reptiles, eight are listed as Vulnerable, six as Near Threatened, and six as Endangered in the IUCN Red List. In the SEMARNAT listing, 19 species are Subject to Special Protection, 26 are Threatened, and three are in Danger of Extinction. -
Craugastor Augusti) in New Mexico Mason J
University of New Mexico UNM Digital Repository Faculty and Staff ubP lications Museum of Southwestern Biology 11-30-2015 Final Report: Status of Barking Frog (Craugastor augusti) in New Mexico Mason J. Ryan Ian M. Latella Jacek Tomasz Giermakowski Howard Snell Follow this and additional works at: https://digitalrepository.unm.edu/msb_fsp Recommended Citation Ryan, M. J., Latella, I. M., Giermakowski, J. T., & Snell, H. (2015). Final Report: Status of Barking Frog (Craugastor augusti) in New Mexico. https://doi.org/10.25844/7922-3R81 This Technical Report is brought to you for free and open access by the Museum of Southwestern Biology at UNM Digital Repository. It has been accepted for inclusion in Faculty and Staff ubP lications by an authorized administrator of UNM Digital Repository. For more information, please contact [email protected]. Final Report: Status of Barking Frog (Craugastor augusti) in New Mexico Delivered to New Mexico Department of Game and Fish on November 30, 2015 Permanently archived in the University of New Mexico Institutional Repository (https://repository.unm.edu/ ) with the identifier http://hdl.handle.net/1928/33082 Project Work Order: #150422 Reporting period: 1 May 2015–30 Nov 2015 Authorship: Mason J Ryan, Ian M Latella, J Tomasz Giermakowski, Howard L Snell University of New Mexico and Museum of Southwestern Biology, Albuquerque, NM. [email protected], 505-277-5130 Suggested citation: Ryan, MJ, IM Latella, JT Giermakowski, HL Snell. 2015. Final Report: Status of Barking Frog (Craugastor augusti) in New Mexico. Submitted to New Mexico Department of Game and Fish; Project Work Order: #150422. Albuquerque, New Mexico: University of New Mexico, November 30, 2015. -
Life History Account for Smith's Black-Headed Snake
California Wildlife Habitat Relationships System California Department of Fish and Wildlife California Interagency Wildlife Task Group SMITH'S BLACK-HEADED SNAKE Tantilla hobartsmithi Family: COLUBRIDAE Order: SQUAMATA Class: REPTILIA R069 Written by: R. Duke Reviewed by: T. Papenfuss Edited by: R. Duke Updated by: CWHR Staff, February 2008 DISTRIBUTION, ABUNDANCE AND SEASONALITY Smith's black-headed snake is an uncommon species found in California in Inyo, San Bernardino, Kings and Tulare cos. Recently redescribed (Cole and Hardy 1981), the species may be more widespread and common but few data are available. May also be present in Kern and Fresno cos., but there are no verified records. Elsewhere, the species ranges patchily throughout the southwest and into Mexico. These secretive, fossorial snakes are found in a variety of arid habitats, including desert riparian, pine-juniper, sagebrush, alkali scrub, Joshua tree and perennial grass. Ranges up to 1440 m (4750 ft) in the Kingston Mts, San Bernardino Co. (Stebbins 1954, Banta 1960, Cole and Hardy 1981, 1983). SPECIFIC HABITAT REQUIREMENTS Feeding: The few records available indicate a preference for invertebrate prey. Beetle larvae, and centipedes have been reported (Minton 1959). Millipedes, spiders and other invertebrates are probably taken as well. Cover: Fossorial. Friable, organic or sandy soil probably required. The species is often found under loose boards, logs, wood, rocks and fallen shrubs. Reproduction: Habitat requirements are unknown. Eggs are probably laid in crevices, rotting logs, or abandoned mammal burrows. Water: No data. More common near water sources. Pattern: Prefers moist niches in otherwise arid or semi-arid habitats, with debris, and friable soil. -
Ecography ECOG-01369 Cunningham, H
Ecography ECOG-01369 Cunningham, H. R., Rissler, L. J., Buckley, L. B. and Urban, M. C. 2015. Abiotic and biotic constraints across reptile and amphibian ranges. – Ecography doi: 10.1111/ecog.01369 Supplementary material Appendix 1 TABLE A1 The directional offsets and linear distances between the centroid of the observed and predicted range for all species. The ratio of predicted to actual range area North (Pn) or South (Ps) of the observed geometric centroids is listed for each species. If the ratio of habitat predicted to be suitable in the South and North (Ps/Pn) is greater than one, there is more overprediction in the South. Species with ranges abutting the Gulf of Mexico were excluded from the analysis. 31 Offset Offset Climate Sample Species Class Order Region Vector Distance Ps Pn Ps/Pn Variable of Size (degrees) (km) Importance Anaxyrus Amphibian Anura East 9.61 372.4 0.85 0.79 1.07 2231 16 americanus Lithobates Amphibian Anura East 26.79 329.49 0.35 0.37 0.95 41 1 septentrionalis Lithobates Amphibian Anura East 303.63 2018.7 0.17 0.24 0.72 194 15 sylvaticus Rhinophrynus Amphibian Anura East 261.13 78.85 2.09 1.33 1.57 35 7 dorsalis Anaxyrus boreas Amphibian Anura West 347.46 1616.8 7.21 7 1.03 1036 11 Anaxyrus Amphibian Anura West 168.77 502.33 16.2 5.86 2.76 7 18 californicus Anaxyrus canorus Amphibian Anura West 171.59 290.62 7 13 0.54 64 8 Anaxyrus cognatus Amphibian Anura West 349.05 98.12 0.89 0.98 0.91 577 2 Anaxyrus Amphibian Anura West 319.04 658.3 0.86 1.08 0.79 15 1 hemiophrys Anaxyrus punctatus Amphibian Anura West -
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often be ingested at night. A subsequent study on the acceptance of dead prey by snakes was undertaken by curator Edward George Boulenger in 1915 (Proc. Zool. POINTS OF VIEW Soc. London 1915:583–587). The situation at the London Zoo becomes clear when one refers to a quote by Mitchell in 1929: “My rule about no living prey being given except with special and direct authority is faithfully kept, and permission has to be given in only the rarest cases, these generally of very delicate or new- Herpetological Review, 2007, 38(3), 273–278. born snakes which are given new-born mice, creatures still blind and entirely un- © 2007 by Society for the Study of Amphibians and Reptiles conscious of their surroundings.” The Destabilization of North American Colubroid 7 Edward Horatio Girling, head keeper of the snake room in 1852 at the London Zoo, may have been the first zoo snakebite victim. After consuming alcohol in Snake Taxonomy prodigious quantities in the early morning with fellow workers at the Albert Public House on 29 October, he staggered back to the Zoo and announced that he was inspired to grab an Indian cobra a foot behind its head. It bit him on the nose. FRANK T. BURBRINK* Girling was taken to a nearby hospital where current remedies available at the time Biology Department, 2800 Victory Boulevard were tried: artificial respiration and galvanism; he died an hour later. Many re- College of Staten Island/City University of New York spondents to The Times newspaper articles suggested liberal quantities of gin and Staten Island, New York 10314, USA rum for treatment of snakebite but this had already been accomplished in Girling’s *Author for correspondence; e-mail: [email protected] case.