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Herpetological Information Service No
Type Descriptions and Type Publications OF HoBART M. Smith, 1933 through June 1999 Ernest A. Liner Houma, Louisiana smithsonian herpetological information service no. 127 2000 SMITHSONIAN HERPETOLOGICAL INFORMATION SERVICE The SHIS series publishes and distributes translations, bibliographies, indices, and similar items judged useful to individuals interested in the biology of amphibians and reptiles, but unlikely to be published in the normal technical journals. Single copies are distributed free to interested individuals. Libraries, herpetological associations, and research laboratories are invited to exchange their publications with the Division of Amphibians and Reptiles. We wish to encourage individuals to share their bibliographies, translations, etc. with other herpetologists through the SHIS series. If you have such items please contact George Zug for instructions on preparation and submission. Contributors receive 50 free copies. Please address all requests for copies and inquiries to George Zug, Division of Amphibians and Reptiles, National Museum of Natural History, Smithsonian Institution, Washington DC 20560 USA. Please include a self-addressed mailing label with requests. Introduction Hobart M. Smith is one of herpetology's most prolific autiiors. As of 30 June 1999, he authored or co-authored 1367 publications covering a range of scholarly and popular papers dealing with such diverse subjects as taxonomy, life history, geographical distribution, checklists, nomenclatural problems, bibliographies, herpetological coins, anatomy, comparative anatomy textbooks, pet books, book reviews, abstracts, encyclopedia entries, prefaces and forwords as well as updating volumes being repnnted. The checklists of the herpetofauna of Mexico authored with Dr. Edward H. Taylor are legendary as is the Synopsis of the Herpetofalhva of Mexico coauthored with his late wife, Rozella B. -
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. -
Summary of Amphibian Community Monitoring at Canaveral National Seashore, 2009
National Park Service U.S. Department of the Interior Natural Resource Program Center Summary of Amphibian Community Monitoring at Canaveral National Seashore, 2009 Natural Resource Data Series NPS/SECN/NRDS—2010/098 ON THE COVER Clockwise from top left, Hyla chrysoscelis (Cope’s grey treefrog), Hyla gratiosa (barking treefrog), Scaphiopus holbrookii (Eastern spadefoot), and Hyla cinerea (Green treefrog). Photographs by J.D. Willson. Summary of Amphibian Community Monitoring at Canaveral National Seashore, 2009 Natural Resource Data Series NPS/SECN/NRDS—2010/098 Michael W. Byrne, Laura M. Elston, Briana D. Smrekar, Brent A. Blankley, and Piper A. Bazemore USDI National Park Service Southeast Coast Inventory and Monitoring Network Cumberland Island National Seashore 101 Wheeler Street Saint Marys, Georgia, 31558 October 2010 U.S. Department of the Interior National Park Service Natural Resource Program Center Fort Collins, Colorado The National Park Service, Natural Resource Program Center publishes a range of reports that address natural resource topics of interest and applicability to a broad audience in the National Park Service and others in natural resource management, including scientists, conservation and environmental constituencies, and the public. The Natural Resource Data Series is intended for timely release of basic data sets and data summaries. Care has been taken to assure accuracy of raw data values, but a thorough analysis and interpretation of the data has not been completed. Consequently, the initial analyses of data in this report are provisional and subject to change. All manuscripts in the series receive the appropriate level of peer review to ensure that the information is scientifically credible, technically accurate, appropriately written for the intended audience, and designed and published in a professional manner. -
Herpetofaunal Inventories of the National Parks of South Florida and the Caribbean: Volume IV
Herpetofaunal Inventories of the National Parks of South Florida and the Caribbean: Volume IV. Biscayne National Park By Kenneth G. Rice1, J. Hardin Waddle1, Marquette E. Crockett 2, Christopher D. Bugbee2, Brian M. Jeffery 2, and H. Franklin Percival 3 1 U.S. Geological Survey, Florida Integrated Science Center 2 University of Florida, Department of Wildlife Ecology and Conservation 3 Florida Cooperative Fish and Wildlife Research Unit Open-File Report 2007-1057 U.S. Department of the Interior U.S. Geological Survey U.S. Department of the Interior DIRK KEMPTHORNE, Secretary U.S. Geological Survey Mark D. Myers, Director U.S. Geological Survey, Reston, Virginia: 2007 For product and ordering information: World Wide Web: http://www.usgs.gov/pubprod Telephone: 1-888-ASK-USGS Any use of trade, product, or firm names is for descriptive purposes only and does not imply endorsement by the U.S. Government. Although this report is in the public domain, permission must be secured from the individual copyright owners to reproduce any copyrighted materials contained within this report. Suggested citation: Rice, K.G., Waddle, J.H., Crockett, M.E., Bugbee, C.D., Jeffery, B.M., and Percival, H.F., 2007, Herpetofaunal Inventories of the National Parks of South Florida and the Caribbean: Volume IV. Biscayne National Park: U.S. Geological Survey Open-File Report 2007-1057, 65 p. Online at: http://pubs.usgs.gov/ofr/2007/1057/ For more information about this report, contact: Dr. Kenneth G. Rice U.S. Geological Survey Florida Integrated Science Center UF-FLREC 3205 College Ave. Ft. Lauderdale, FL 33314 USA E-mail: [email protected] Phone: 954-577-6305 Fax: 954-577-6347 Dr. -
Site-Specific Environmental Assessment
Environmental Assessment Rangeland Grasshopper and Mormon Cricket Suppression Program ARIZONA EA Number: AZ-20-01 Site-Specific Graham and Gila County portion within the San Carlos Apache Reservation; Mohave County Hualapai Reservation; Cochise County portion of Coronado National Forest – Winchester Mountains Prepared by: Animal and Plant Health Inspection Service 3640 East Wier Ave. Phoenix, Arizona 85040 May 6, 2020 1 Table of Contents I. Need for Proposed Action ...................................................................................................... 4 A. Purpose and Need Statement .............................................................................................. 4 B. Background Discussion ...................................................................................................... 5 C. About This Process ............................................................................................................. 7 II. Alternatives ............................................................................................................................ 7 A. No Action Alternative ......................................................................................................... 8 B. Insecticide Applications at Conventional Rates or Reduced Agent Area Treatments with Adaptive Management Strategy (Preferred Alternative) .......................................................................... 8 C. Experimental Treatments Alternative .............................................................................. -
Venom On-A-Chip: a Fast and Efficient Method for Comparative Venomics
toxins Article Venom On-a-Chip: A Fast and Efficient Method for Comparative Venomics Giulia Zancolli 1,*, Libia Sanz 2, Juan J. Calvete 2 and Wolfgang Wüster 1,* 1 Molecular Ecology and Fisheries Genetics Lab, School of Biological Sciences, Bangor University, Bangor LL57 2UW, UK 2 Venomics and Structural Proteomics Laboratory, Instituto de Biomedicina de Valencia, CSIC, Jaume Roig 11, Valencia 46010, Spain; [email protected] (L.S.); [email protected] (J.J.C.) * Correspondence: [email protected] (G.Z.); [email protected] (W.W.) Academic Editor: Kevin Arbuckle Received: 20 April 2017; Accepted: 24 May 2017; Published: 28 May 2017 Abstract: Venom research has attracted an increasing interest in disparate fields, from drug development and pharmacology, to evolutionary biology and ecology, and rational antivenom production. Advances in “-omics” technologies have allowed the characterization of an increasing number of animal venoms, but the methodology currently available is suboptimal for large-scale comparisons of venom profiles. Here, we describe a fast, reproducible and semi-automated protocol for investigating snake venom variability, especially at the intraspecific level, using the Agilent Bioanalyzer on-chip technology. Our protocol generated a phenotype matrix which can be used for robust statistical analysis and correlations of venom variation with ecological correlates, or other extrinsic factors. We also demonstrate the ease and utility of combining on-chip technology with previously fractionated venoms for detection of specific individual toxin proteins. Our study describes a novel strategy for rapid venom discrimination and analysis of compositional variation at multiple taxonomic levels, allowing researchers to tackle evolutionary questions and unveiling the drivers of the incredible biodiversity of venoms. -
211356675.Pdf
306.1 REPTILIA: SQUAMATA: SERPENTES: COLUBRIDAE STORERIA DEKA YI Catalogue of American Amphibians and Reptiles. and western Honduras. There apparently is a hiatus along the Suwannee River Valley in northern Florida, and also a discontin• CHRISTMAN,STEVENP. 1982. Storeria dekayi uous distribution in Central America . • FOSSILRECORD. Auffenberg (1963) and Gut and Ray (1963) Storeria dekayi (Holbrook) recorded Storeria cf. dekayi from the Rancholabrean (pleisto• Brown snake cene) of Florida, and Holman (1962) listed S. cf. dekayi from the Rancholabrean of Texas. Storeria sp. is reported from the Ir• Coluber Dekayi Holbrook, "1836" (probably 1839):121. Type-lo• vingtonian and Rancholabrean of Kansas (Brattstrom, 1967), and cality, "Massachusetts, New York, Michigan, Louisiana"; the Rancholabrean of Virginia (Guilday, 1962), and Pennsylvania restricted by Trapido (1944) to "Massachusetts," and by (Guilday et al., 1964; Richmond, 1964). Schmidt (1953) to "Cambridge, Massachusetts." See Re• • PERTINENT LITERATURE. Trapido (1944) wrote the most marks. Only known syntype (Acad. Natur. Sci. Philadelphia complete account of the species. Subsequent taxonomic contri• 5832) designated lectotype by Trapido (1944) and erroneously butions have included: Neill (195Oa), who considered S. victa a referred to as holotype by Malnate (1971); adult female, col• lector, and date unknown (not examined by author). subspecies of dekayi, Anderson (1961), who resurrected Cope's C[oluber] ordinatus: Storer, 1839:223 (part). S. tropica, and Sabath and Sabath (1969), who returned tropica to subspecific status. Stuart (1954), Bleakney (1958), Savage (1966), Tropidonotus Dekayi: Holbrook, 1842 Vol. IV:53. Paulson (1968), and Christman (1980) reported on variation and Tropidonotus occipito-maculatus: Holbrook, 1842:55 (inserted ad- zoogeography. Other distributional reports include: Carr (1940), denda slip). -
Checklist of Reptiles and Amphibians Revoct2017
CHECKLIST of AMPHIBIANS and REPTILES of ARCHBOLD BIOLOGICAL STATION, the RESERVE, and BUCK ISLAND RANCH, Highlands County, Florida. Voucher specimens of species recorded from the Station are deposited in the Station reference collections and the herpetology collection of the American Museum of Natural History. Occurrence3 Scientific name1 Common name Status2 Exotic Station Reserve Ranch AMPHIBIANS Order Anura Family Bufonidae Anaxyrus quercicus Oak Toad X X X Anaxyrus terrestris Southern Toad X X X Rhinella marina Cane Toad ■ X Family Hylidae Acris gryllus dorsalis Florida Cricket Frog X X X Hyla cinerea Green Treefrog X X X Hyla femoralis Pine Woods Treefrog X X X Hyla gratiosa Barking Treefrog X X X Hyla squirella Squirrel Treefrog X X X Osteopilus septentrionalis Cuban Treefrog ■ X X Pseudacris nigrita Southern Chorus Frog X X Pseudacris ocularis Little Grass Frog X X X Family Leptodactylidae Eleutherodactylus planirostris Greenhouse Frog ■ X X X Family Microhylidae Gastrophryne carolinensis Eastern Narrow-mouthed Toad X X X Family Ranidae Lithobates capito Gopher Frog X X X Lithobates catesbeianus American Bullfrog ? 4 X X Lithobates grylio Pig Frog X X X Lithobates sphenocephalus sphenocephalus Florida Leopard Frog X X X Order Caudata Family Amphiumidae Amphiuma means Two-toed Amphiuma X X X Family Plethodontidae Eurycea quadridigitata Dwarf Salamander X Family Salamandridae Notophthalmus viridescens piaropicola Peninsula Newt X X Family Sirenidae Pseudobranchus axanthus axanthus Narrow-striped Dwarf Siren X Pseudobranchus striatus -
Xenosaurus Tzacualtipantecus. the Zacualtipán Knob-Scaled Lizard Is Endemic to the Sierra Madre Oriental of Eastern Mexico
Xenosaurus tzacualtipantecus. The Zacualtipán knob-scaled lizard is endemic to the Sierra Madre Oriental of eastern Mexico. This medium-large lizard (female holotype measures 188 mm in total length) is known only from the vicinity of the type locality in eastern Hidalgo, at an elevation of 1,900 m in pine-oak forest, and a nearby locality at 2,000 m in northern Veracruz (Woolrich- Piña and Smith 2012). Xenosaurus tzacualtipantecus is thought to belong to the northern clade of the genus, which also contains X. newmanorum and X. platyceps (Bhullar 2011). As with its congeners, X. tzacualtipantecus is an inhabitant of crevices in limestone rocks. This species consumes beetles and lepidopteran larvae and gives birth to living young. The habitat of this lizard in the vicinity of the type locality is being deforested, and people in nearby towns have created an open garbage dump in this area. We determined its EVS as 17, in the middle of the high vulnerability category (see text for explanation), and its status by the IUCN and SEMAR- NAT presently are undetermined. This newly described endemic species is one of nine known species in the monogeneric family Xenosauridae, which is endemic to northern Mesoamerica (Mexico from Tamaulipas to Chiapas and into the montane portions of Alta Verapaz, Guatemala). All but one of these nine species is endemic to Mexico. Photo by Christian Berriozabal-Islas. Amphib. Reptile Conserv. | http://redlist-ARC.org 01 June 2013 | Volume 7 | Number 1 | e61 Copyright: © 2013 Wilson et al. This is an open-access article distributed under the terms of the Creative Com- mons Attribution–NonCommercial–NoDerivs 3.0 Unported License, which permits unrestricted use for non-com- Amphibian & Reptile Conservation 7(1): 1–47. -
Literature Cited in Lizards Natural History Database
Literature Cited in Lizards Natural History database Abdala, C. S., A. S. Quinteros, and R. E. Espinoza. 2008. Two new species of Liolaemus (Iguania: Liolaemidae) from the puna of northwestern Argentina. Herpetologica 64:458-471. Abdala, C. S., D. Baldo, R. A. Juárez, and R. E. Espinoza. 2016. The first parthenogenetic pleurodont Iguanian: a new all-female Liolaemus (Squamata: Liolaemidae) from western Argentina. Copeia 104:487-497. Abdala, C. S., J. C. Acosta, M. R. Cabrera, H. J. Villaviciencio, and J. Marinero. 2009. A new Andean Liolaemus of the L. montanus series (Squamata: Iguania: Liolaemidae) from western Argentina. South American Journal of Herpetology 4:91-102. Abdala, C. S., J. L. Acosta, J. C. Acosta, B. B. Alvarez, F. Arias, L. J. Avila, . S. M. Zalba. 2012. Categorización del estado de conservación de las lagartijas y anfisbenas de la República Argentina. Cuadernos de Herpetologia 26 (Suppl. 1):215-248. Abell, A. J. 1999. Male-female spacing patterns in the lizard, Sceloporus virgatus. Amphibia-Reptilia 20:185-194. Abts, M. L. 1987. Environment and variation in life history traits of the Chuckwalla, Sauromalus obesus. Ecological Monographs 57:215-232. Achaval, F., and A. Olmos. 2003. Anfibios y reptiles del Uruguay. Montevideo, Uruguay: Facultad de Ciencias. Achaval, F., and A. Olmos. 2007. Anfibio y reptiles del Uruguay, 3rd edn. Montevideo, Uruguay: Serie Fauna 1. Ackermann, T. 2006. Schreibers Glatkopfleguan Leiocephalus schreibersii. Munich, Germany: Natur und Tier. Ackley, J. W., P. J. Muelleman, R. E. Carter, R. W. Henderson, and R. Powell. 2009. A rapid assessment of herpetofaunal diversity in variously altered habitats on Dominica. -
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 -
Red Gap Ranch Biological Resource Evaluation
RED GAP RANCH BIOLOGICAL RESOURCE EVALUATION Prepared for: Southwest Ground-water Consultants, Inc. Prepared by: WestLand Resources, Inc. Date: February 14, 2014 Project No.: 1822.01 TABLE OF CONTENTS 1. BACKGROUND AND OBJECTIVES ................................................................................................ 1 2. EXISTING ENVIRONMENT AND BIOLOGICAL RESOURCES ................................................... 2 2.1. Approach ...................................................................................................................................... 2 2.2. Physical Environment ................................................................................................................... 2 2.3. Biological Environment and Resources ....................................................................................... 3 3. SCREENING ANALYSIS FOR SPECIES OF CONCERN ................................................................ 5 3.1. Approach ...................................................................................................................................... 5 3.2. Screening Analysis Results .......................................................................................................... 7 3.2.1. USFWS-listed Species ...................................................................................................... 7 3.2.2. USFS Coconino National Forest Sensitive Species ........................................................ 15 3.2.3. USFS Management Indicator Species ............................................................................