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At Perris Introduction
FIRE SALE S. San Jacinto Avenue W. 4th Street RESIDENTIAL LAND OPPORTUNITY 20 ACRES ±20 Acres at Perris Introduction Coldwell Banker Commercial So Cal Group has been exclusively retained by ownership to market this 20.14 acre development opportunity in Perris, California. The property is located at the end of Diana Street, near the W. San Jacinto Avenue intersection. The subject property is currently zoned RR - Rural Residential. A rezone to a higher density Residential use would provide a buyer with great upside. W. 4th Street PROPERTY OVERVIEW PROPERTY Navajo Road S. San Jacinto Ave. Industrial Land | Lake Elsinore | California | 92530 3 Property Description Project Location Perris, California Size 20.14 Acres Condition Vacant Assessor’s Parcel No. 326-150-009 Pricing $295,000 ($0.34/SF) Price/Acre $14,647 Zoning RR - Rural Residential PROPERTY OVERVIEW PROPERTY Public Works 1 City Hall 2 Metrolink Station 3 California Military Institute 4 Police Department 3 5 Historical Museum 6 Enchanted Hills Elementary School Surrounding Retail 7 Perris Indoor Swapmeet 4 1 8 2 9 PROPERTY OVERVIEW PROPERTY 6 5 7 10 9 8 10 Industrial Land | Lake Elsinore | California | 92530 7 Riverside Corona Lake Perris Perris 20 Minute Irvine Drive Lake Elsinore Murrieta LOCATION OVERVIEW LOCATION Mission Viejo ORANGE COUNTY San Juan Capistrano Temecula 32 Minute PACIFIC OCEAN Drive Industrial Land | Lake Elsinore | California | 92530 9 Inland Empire Riverside County The largest region of Southern California, the Inland Empire, region. The Inland Empire market continues to be one of Riverside County is one of the fastest growing counties in the United Demographics comprised of both Riverside and San Bernardino Counties, the largest and most dynamic areas in the country, with States, leading the rapidly changing Inland Empire market, with rivers, is one of the most significant economies in the United diminishing land supply as well as steady absorption and mountain peaks, deserts and fertile valleys, Riverside County offers Census 2010 Summary States. -
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. -
California Citrus State Historic Park 9400 Dufferin Ave
Our Mission California The mission of California State Parks is to provide for the health, inspiration and rassy, tree-shaded education of the people of California by helping G Citrus to preserve the state’s extraordinary biological diversity, protecting its most valued natural and areas evoke a quieter cultural resources, and creating opportunities State Historic Park for high-quality outdoor recreation. time — an era when the American dream might be found in a leafy evergreen grove, heavy California State Parks supports equal access. with golden fruit. Prior to arrival, visitors with disabilities who need assistance should contact the park at (951) 780-6222. If you need this publication in an alternate format, contact [email protected]. CALIFORNIA STATE PARKS P.O. Box 942896 Sacramento, CA 94296-0001 For information call: (800) 777-0369 (916) 653-6995, outside the U.S. 711, TTY relay service www.parks.ca.gov California Citrus State Historic Park 9400 Dufferin Ave. / Mail: 1879 Jackson St. Riverside, CA 92504 (951) 780-6222 © 2003 California State Parks (Rev. 2016) V isitors to California Citrus State NATIVE PEOPLE trauma, honoring their Historic Park are greeted at the park The area that is now Riverside County was cultural traditions, and entrance by a replica of an old-fashioned inhabited for centuries by diverse native contributing as vital roadside fruit stand. This charming “big peoples, including Serrano, Luiseño, community members. orange” structure, on the corner of Van Gabrielino-Tongva, Cupeño, Chemehuevi, CREATING THE Buren Boulevard and Dufferin Avenue in and Cahuilla. California Indians traveled CITRUS INDUSTRY Riverside, recalls an era that forever changed seasonally from village to village, following the landscape their food sources and The mission padres of Southern trade routes. -
A Review of the Cnemidophorus Lemniscatus Group in Central America (Squamata: Teiidae), with Comments on Other Species in the Group
TERMS OF USE This pdf is provided by Magnolia Press for private/research use. Commercial sale or deposition in a public library or website is prohibited. Zootaxa 3722 (3): 301–316 ISSN 1175-5326 (print edition) www.mapress.com/zootaxa/ Article ZOOTAXA Copyright © 2013 Magnolia Press ISSN 1175-5334 (online edition) http://dx.doi.org/10.11646/zootaxa.3722.3.1 http://zoobank.org/urn:lsid:zoobank.org:pub:4E9BA052-EEA9-4262-8DDA-E1145B9FA996 A review of the Cnemidophorus lemniscatus group in Central America (Squamata: Teiidae), with comments on other species in the group JAMES R. MCCRANIE1,3 & S. BLAIR HEDGES2 110770 SW 164th Street, Miami, Florida 33157-2933, USA. E-mail: [email protected] 2Department of Biology, 208 Mueller Laboratory, Pennsylvania State University, University Park, Pennsylvania 16802-5301, USA. E-mail: [email protected] 3Corresponding author. E-mail: [email protected] Abstract We provide the results of a morphological and molecular study on the Honduran Bay Island and mainland populations of the Cnemidophorus lemniscatus complex for which we resurrect C. ruatanus comb. nov. as a full species. Morphological comparison of the Honduran populations to Cnemidophorus populations from Panama led to the conclusion that the Pan- amanian population represents an undescribed species named herein. In light of these new results, and considering past morphological studies of several South American populations of the C. lemniscatus group, we suggest that three other nominal forms of the group are best treated as valid species: C. espeuti (described as a full species, but subsequently treat- ed as a synonym of C. lemniscatus or a subspecies of C. -
Life History of the Marbled Whiptail Lizard Aspidoscelis Marmorata from the Central Chihuahuan Desert, Mexico
Acta Herpetologica 8(2): 81-91, 2013 Life history of the Marbled Whiptail Lizard Aspidoscelis marmorata from the central Chihuahuan Desert, Mexico Héctor Gadsden1, Gamaliel Castañeda2 1 Instituto de Ecología, A. C.-Centro Regional Chihuahua, Cubículo 29C, Miguel de Cervantes No. 120, Complejo Industrial Chihuahua, C. P. 31109, Chihuahua, Chihuahua, México. Corresponding author. E-mail: [email protected] 2 Facultad de Ciencias Biológicas. Universidad Juárez del Estado de Durango. Avenida Universidad s/n. Fraccionamiento Filadelfia. Gómez Palacio, 35070, Durango, México Submitted on 2012, 5th December; revised on 2013, 10th August; accepted on 2013, 3rd September. Abstract. The life history of a population of marbled whiptail lizard, Aspidoscelis marmorata, was examined from 1989 to 1994 in the sand dunes of the Biosphere Reserve of Mapimí, in Northern México. Lizards were studied using mark- recapture techniques. Reproduction in females occurred between May and August, with birth hatchlings matching the wet season in August. Reproductive activity was highest in the early wet season (July). Males and females reached adult size class at an average age of 1.7 years and 1.8 years, respectively. Body size of males attained an asymptote around 90 mm snout-vent length and females around 82 mm snout-vent length, at an age of approximately 3.6 years and 3.0 years, respectively. The density varied from 7 to 85 individuals / 1.0 ha. The Mexican population had late maturity, relatively long life expectancy, and fewer offspring. Overall, the observed data for A. marmorata and the expectations of life history theory for a late maturing species (K-rate selection) are in agreement. -
Sexual Dimorphism and Natural History of the Western Mexico Whiptail, Aspidoscelis Costata (Squamata: Teiidae), from Isla Isabel, Nayarit, Mexico
NORTH-WESTERN JOURNAL OF ZOOLOGY 10 (2): 374-381 ©NwjZ, Oradea, Romania, 2014 Article No.: 141506 http://biozoojournals.ro/nwjz/index.html Sexual dimorphism and natural history of the Western Mexico Whiptail, Aspidoscelis costata (Squamata: Teiidae), from Isla Isabel, Nayarit, Mexico Raciel CRUZ-ELIZALDE1, Aurelio RAMÍREZ-BAUTISTA1, *, Uriel HERNÁNDEZ-SALINAS1,2, Cynthia SOSA-VARGAS3, Jerry D. JOHNSON4 and Vicente MATA-SILVA4 1. Centro de Investigaciones Biológicas (CIB), Universidad Autónoma del Estado de Hidalgo, Carretera Pachuca-Tulancingo, Km 4.5 s/n, Colonia Carboneras, Mineral de La Reforma, A.P. 1-69 Plaza Juárez, C.P. 42001, Hidalgo, México. 2. Instituto Politécnico Nacional, CIIDIR Unidad Durango, Sigma 119, Fraccionamiento 20 de Noviembre II, Durango, Durango 34220, México. 3. Laboratorio de Herpetología, Escuela de Biología, Benemérita Universidad Autónoma de Puebla, C. U. Boulevard Valsequillo y Av. San Claudio, Edif. 76, CP. 72570, Puebla, Puebla, México. 4. Department of Biological Sciences, University of Texas at El Paso, 500 West University Avenue, El Paso, TX 79968, USA. *Corresponding author, A. Ramírez-Bautista, E-mail: [email protected] Received: 25. April 2014 / Accepted: 13. June 2014 / Available online: 16. October 2014 / Printed: December 2014 Abstract. Lizard populations found in insular environments may show ecological and morphological characteristics that differ from those living in continents, as a result of different ecological and evolutionary processes. In this study, we analyzed sexual dimorphism, reproduction, and diet in a population of the whiptail lizard, Aspidoscelis costata, from Isla Isabel, Nayarit, Mexico, sampled in 1977 and 1981. Males and females from Isla Isabel showed no sexual dimorphism in many morphological structures, such as snout-vent length (SVL), but they did in femur length (FL) and tibia length (TL). -
Taxonomic Hypotheses and the Biogeography of Speciation in the Tiger Whiptail Complex (Aspidoscelis Tigris: Squamata, Teiidae)
a Frontiers of Biogeography 2021, 13.2, e49120 Frontiers of Biogeography RESEARCH ARTICLE the scientific journal of the International Biogeography Society Taxonomic hypotheses and the biogeography of speciation in the Tiger Whiptail complex (Aspidoscelis tigris: Squamata, Teiidae) Tyler K. Chafin1* , Marlis R. Douglas1 , Whitney J.B. Anthonysamy1,2, Brian K. Sullivan3, James M. Walker1, James E. Cordes4, and Michael E. Douglas1 1 Department of Biological Sciences, University of Arkansas, Fayetteville, Arkansas, 72701, USA; 2 St. Louis College of Pharmacy, 4588 Parkview Place, St. Louis, Missouri, 63110, USA; 3 School of Mathematical and Natural Sciences, P. O. Box 37100, Arizona State University, Phoenix, Arizona, 85069, USA; 4 Division of Mathematics and Sciences, Louisiana State University, Eunice, Louisiana, 70535, USA. *Corresponding author: Tyler K. Chafin, [email protected] Abstract Highlights Biodiversity in southwestern North America has a complex 1. Phylogeographies of vertebrates within the biogeographic history involving tectonism interspersed southwestern deserts of North America have been with climatic fluctuations. This yields a contemporary shaped by climatic fluctuations imbedded within pattern replete with historic idiosyncrasies often difficult broad geomorphic processes. to interpret when viewed from through the lens of modern ecology. The Aspidoscelis tigris (Tiger Whiptail) 2. The resulting synergism drives evolutionary processes, complex (Squamata: Teiidae) is one such group in which such as an expansion of within-species genetic taxonomic boundaries have been confounded by a series divergence over time. Taxonomic inflation often of complex biogeographic processes that have defined results (i.e., an increase in recognized taxa due to the evolution of the clade. To clarify this situation, arbitrary delineations), such as when morphological we first generated multiple taxonomic hypotheses, divergences fail to juxtapose with biogeographic which were subsequently tested using mitochondrial hypotheses. -
California State Parks
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0189 Xantusia Henshawi.Pdf (296.1Kb)
189.1 REPTILIA: SQUAMATA: SAURIA: XANTUSIIDAE XANTUSIA HENSHA WI Catalogue of Am.erican Am.phihians and Reptiles. sequently (Van Denburgh, 1922) placed Z ablepsis henshavii in the synonymy ofX. henshawi Stejneger. Cope (1895b) described, LEE, JULIANC. 1976. Xantusia henshawi. but failed to name a supposedly new species of Xantusia. In a later publication (Cope, 1895c) he corrected the oversight, and named Xantusia picta. Van Denburgh (1916) synonymized Xantusia henshawi Stejneger picta with X. henshawi, and traced the complicated history of Granite night lizard the type-specimen . Xantusia henshawi Stejneger, 1893:467. Type-locality, "Witch • ETYMOLOGY.The specific epithet honors H. W. Henshaw. Creek, San Diego County, California." Holotype, U. S. Nat. According to Webb (1970), "The name bolsonae refers to the Mus. 20339, collected in May 1893 by H. W. Henshaw (Holo• geographic position of this race in a southern outlier of the type not seen by author). Bolson de Mapimi." Zablepsis henshavii: Cope, 1895a:758. See NOMENCLATURAL HISTORY. 1. Xantusia henshawi henshawi Stejnege •. Xantusia picta Cope, 1895c:859. Type-locality, "Tejon Pass, California," probably in error, corrected by Van Denburgh Xantusia henshawi Stejneger, 1893:467. See species account. Xantusia henshawi henshawi: Webb, 1970:2. First use of tri- (1916:14) to Poway, San Diego County, California. Holotype, nomial. Acad. Natur. Sci. Philadelphia 12881 (Malnate, 1971), prob• ably collected by Dr. Frank E. Blaisdell (see NOMENCLATURAL • DEFINITIONANDDIAGNOSIS. The mean snout-vent length HISTORY). in males is 56 mm., and in females 62 mm. Distinct post• • CONTENT. Two subspecies are recognized: henshawi and orbital stripes are usually absent, and the dorsal color pattern bolsonae. -
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. -
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