Gecko Enano, Lepidoblepharis Miyatai
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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. -
From Four Sites in Southern Amazonia, with A
Bol. Mus. Para. Emílio Goeldi. Cienc. Nat., Belém, v. 4, n. 2, p. 99-118, maio-ago. 2009 Squamata (Reptilia) from four sites in southern Amazonia, with a biogeographic analysis of Amazonian lizards Squamata (Reptilia) de quatro localidades da Amazônia meridional, com uma análise biogeográfica dos lagartos amazônicos Teresa Cristina Sauer Avila-PiresI Laurie Joseph VittII Shawn Scott SartoriusIII Peter Andrew ZaniIV Abstract: We studied the squamate fauna from four sites in southern Amazonia of Brazil. We also summarized data on lizard faunas for nine other well-studied areas in Amazonia to make pairwise comparisons among sites. The Biogeographic Similarity Coefficient for each pair of sites was calculated and plotted against the geographic distance between the sites. A Parsimony Analysis of Endemicity was performed comparing all sites. A total of 114 species has been recorded in the four studied sites, of which 45 are lizards, three amphisbaenians, and 66 snakes. The two sites between the Xingu and Madeira rivers were the poorest in number of species, those in western Amazonia, between the Madeira and Juruá Rivers, were the richest. Biogeographic analyses corroborated the existence of a well-defined separation between a western and an eastern lizard fauna. The western fauna contains two groups, which occupy respectively the areas of endemism known as Napo (west) and Inambari (southwest). Relationships among these western localities varied, except between the two northernmost localities, Iquitos and Santa Cecilia, which grouped together in all five area cladograms obtained. No variation existed in the area cladogram between eastern Amazonia sites. The easternmost localities grouped with Guianan localities, and they all grouped with localities more to the west, south of the Amazon River. -
REPTILIA: SQUAMATA: GEKKONIDAE Thecadactylus Goldfuss I
REPTILIA: SQUAMATA: GEKKONIDAE THECADACTYLUS,T. RAPICAUDA Catalogue of American Amphibians and Reptiles. ETYMOLOGY. Thecadacrylus is derived from the Latin th- eta, meaning sheath, and dactylus, from the Greek daktylos Russell, A.P. and A.M. Bauer. 2002. Thecadactylus, T. rapi- meaning finger. The name refers to the sheathed claws that are cauda. diagnostic for this genus. Thecadactylus Goldfuss REMARKS. Cuvier (I817 [1816]) used the vernacular term "thecadactyles" in reference to several species of geckos, but Thecadactylus Goldfuss 1820: 157. Qpe species, Gecko laevis did not use a Latinized generic name. Goldfuss (l820), whose Daudin 1802:112 (= Thecadactylus rapicauda [Houttuyn citation of the name Thecadactylus in conjunction with the spe- 1782]), by monotypy. cies laevis made the name available, attributed the name to Thecodac~lus:Wagler 1830:142. Nomen substitutum. Cuvier. Avila-Pires ( 1995) attributed the name Thecadactylus Thecadacrylus: Amaral1948 (1949): 109. Error typographicus. to Oken (1817). but this usage, in a summary of Cuvier's (1817 Tecadactylus: Medina 1973:318. Lapsus. [1816]) classification system, has been regarded as a nomen nudum (e.g., Kluge 1993). Vanzolini (1968a) reviewed the his- CONTENT. A single species, Thecadactylus rapicauda, is tory of the generic name and incorrectly attributed it to Gray recognized (Kluge 1991, 1993; Rosler 2000). (1825). DEFINITION, DIAGNOSIS, DESCRIPTIONS, ILLUS- TRATIONS, DISTRIBUTION, FOSSIL RECORD, PERTI- NENT LITERATURE. See species account. HU~RUJ.r\uurt r rrrruuoLryrrr> rupLuuuu wlur rcgcr~crar~utat, rrutfl Rio Ituxi, Amazonas, Brazil (photograph by L.J. Vitt). FIGURE 4. Adult Thecadactylus rapicauda from Rio Formoso, RodBnia, Brazil, illustrating the golden colored iris and a dark dorsal pattern (photograph by L.J. -
Lepidoblepharis Sanctaemartae (RUTHVEN, 1916)
ZOBODAT - www.zobodat.at Zoologisch-Botanische Datenbank/Zoological-Botanical Database Digitale Literatur/Digital Literature Zeitschrift/Journal: Herpetozoa Jahr/Year: 2002 Band/Volume: 15_1_2 Autor(en)/Author(s): Rivas Fuenmayor Gilson, Manzanilla Jesus, Rivero Ramon, La Marca Enrique Artikel/Article: Lepidoblepharis sanctaemartae (RUTHVEN, 1916), a lizard new to the Venezuelan fauna 92-94 ©Österreichische Gesellschaft für Herpetologie e.V., Wien, Austria, download unter www.biologiezentrum.at 92 SHORT NOTE HERPETOZOA 15 (1/2) Wien, 30. Juni 2002 SHORT NOTE ales del Museo de Zoologìa, Mexico, DF; 9: 1-48. ela, at elevations between 50 and 70 m, one ETHERIDGE, R. E. (1982): Checklist of the the iguanine of us (RR) collected eight specimens of and Malagasy iguanid lizards, pp. 7-37. In: BURG- HARDT, G M. & RAND, A. S. (eds.): Iguanas of the Lepidoblepharis sanctaemartae (RUTHVEN, world. Park Ridge, N. J. (Noyes Pubi.), 472 pp. 1916) (fig. 1). The specimens were pre- GRJSMER, L. L. (1999): An evolutionary classification served in 10% formalin, transferred to 70% of reptiles on islands in the Gulf of California, México.- ethanol, and deposited in the Museo de la Herpetologica, Johnson City; 55 (4): 446-469. INEGI [Institute Nacional de Estadistica Geografia e Infor- Estación Biològica de Rancho Grande, esta- matica] (1992): Sintesis Geografica del Estado de do Aragua, Venezuela (EBRG). Hidalgo. 134 pp. KÖHLER, G & HASBUN, C. R. (2001): The specimens were active in the leaf A new species of spiny-tailed iguana from Mexico for- merly referred to Ctenosaura quinquecarinata (GRAY litter from 10.00 a.m. to 03.00 p.m. in semi- 1842) (Reptilia, Squamata, Iguanidae).- Sencken- deciduous forest ("bosque hümedo premon- bergiana biologica, Frankfurt a. -
Lepidoblepharis Sanctaemartae, Sabanas De San Ángel, Magdalena, Colombia
Lepidoblepharis sanctaemartae, Sabanas de San Ángel, Magdalena, Colombia. Photo by Juan Manuel Renjifo. Amphib. Reptile Conserv. 33 April 2015 | Volume 8 | Number 1 | e92 Official journal website: Amphibian & Reptile Conservation amphibian-reptile-conservation.org 8(1) [General Section]: 33–52 (e92). Amphibians and reptiles of an agroforestry system in the Colombian Caribbean 1Oscar Angarita-M., 2Andrés Camilo Montes-Correa, and 3Juan Manuel Renjifo Grupo de Investigación en Manejo y Conservación de Fauna, Flora y Ecosistemas Estratégicos Neotropicales (MIKU), Universidad del Magdalena, COLOMBIA Abstract.—Land-use change is a factor that may alter the assembly of herpetofaunal communities. To determine the effects of land use change, we characterized the herpetofaunal community of “La Gloria Project” in Magdalena, Colombia. Agroforestry crops (Red Gum, Pink Trumpet Tree, Beechwood, and Teak), native forest, wetlands, and built-up zones composing the site. From March to October 2012, we performed eleven field trips, of ten days (eight hours each) for a total sampling effort of 880 hours per observer. We implemented visual encounter surveys and pitfall traps for herpetofauna detection. We recorded 23 amphibian (3,555 individuals) and 37 reptile species (1,088 individuals); the highest diversity for both amphibians and reptiles were found in native forest. Comparing disturbed areas, Teak agroforest presented the highest diversity for both taxa relative to non-natural environments, by factors such as big leaf size, generating conditions to sustenance of some species. However, we demonstrated that short-term differences between natural and non- natural habitats are significant, since there has not been enough time for generalist species to displace the susceptible species and occupy their niches in all vegetation coverages in the study area. -
Proceedings of the United States National Museum ^^^5^^
Proceedings of the United States National Museum ^^^5^^ SMITHSONIAN INSTITUTION . WASHINGTON, D.C. THE LIZARDS OF ECUADOR, A CHECK LIST AND KEY By James A. Peters Curator, Division of Reptiles This paper constitutes the second of a series devoted to the establishment of a framework upon which additional studies on the ecology and zoogeog- raphy of the Ecuadorian herpetofauna can be based. The first paper dealt with the snakes (J. Peters, 1960), and later studies will be concerned with the amphibians. The principle established in the earlier list has been abrogated, at least in part, since I have been forced to revise the genus Ameiva strictly on the basis of the Ecuadorian political unit. But I repeat my earlier opinion that such analyses are dangerous and can easily result in perpetuation of difficulties. Methods The method of organization in this check list is the same as that of the list of Ecuadorian snakes (J. Peters, 1960). The genera are presented alphabetically, and the species are alphabetical within their genus. It is, I think, true that the average user of the list will be interested in ease and speed of use, not in my contribution to the intricacies of the higher categories i 2 PROCEEDINGS OF THE NATIONAL MUSEUM vol. 119 of lizard classification (the basic phylogenetic position of the genera con- cerned is presented on p. 3), For each taxon I have presented a very brief synonymy, beginning with a citation to the original description of that taxon and its type locality, plus the holotype and its location in paren- theses. -
Evolution and Ecology of Lizard Body Sizes PAPER Shai Meiri
Global Ecology and Biogeography, (Global Ecol. Biogeogr.) (2008) 17, 724–734 Blackwell Publishing Ltd RESEARCH Evolution and ecology of lizard body sizes PAPER Shai Meiri NERC Centre for Population Biology, Imperial ABSTRACT College London, Silwood Park, Ascot, Berkshire Aim Body size is instrumental in influencing animal physiology, morphology, SL5 7PY, UK ecology and evolution, as well as extinction risk. I examine several hypotheses regarding the influence of body size on lizard evolution and extinction risk, assessing whether body size influences, or is influenced by, species richness, herbivory, island dwelling and extinction risk. Location World-wide. Methods I used literature data and measurements of museum and live specimens to estimate lizard body size distributions. Results I obtained body size data for 99% of the world’s lizard species. The body size–frequency distribution is highly modal and right skewed and similar distributions characterize most lizard families and lizard assemblages across biogeographical realms. There is a strong negative correlation between mean body size within families and species richness. Herbivorous lizards are larger than omnivorous and carnivorous ones, and aquatic lizards are larger than non-aquatic species. Diurnal activity is associated with small body size. Insular lizards tend towards both extremes of the size spectrum. Extinction risk increases with body size of species for which risk has been assessed. Main conclusions Small size seems to promote fast diversification of disparate body plans. The absence of mammalian predators allows insular lizards to attain larger body sizes by means of release from predation and allows them to evolve into the top predator niche. Island living also promotes a high frequency of herbivory, which is also associated with large size. -
Communal Egg-Laying and Hatchling Size in the Pygmy Gecko Coleodactylus Natalensis (Squamata: Sphaerodactylidae) in an Atlantic Forest Site of Brazil
Herpetology Notes, volume 13: 377-383 (2020) (published online on 15 May 2020) Communal egg-laying and hatchling size in the pygmy gecko Coleodactylus natalensis (Squamata: Sphaerodactylidae) in an Atlantic Forest site of Brazil Raul F. D. Sales1,*, Olyana S. Furtado1, Daniel L. Santos-Junior1, Vinicius T. C. Silva1, André F. V. Duarte1, and Eliza M. X. Freire1 Abstract. Knowing the biology and natural history of a species is the first step to formulate conservation strategies. In this perspective, this study reports new data about the reproductive biology of Coleodactylus natalensis, an endemic and threatened species from Atlantic Forest remnants of Northeast Brazil. Our observations took place at the Floresta Nacional de Nísia Floresta, a protected area of Rio Grande do Norte state, during the months of March and April 2019. Along the 32 inspected quadrants (50 m2 each), we recorded a total of 18 eggs of C. natalensis in six distinct egg sites, all of them found in the soil below the leaf litter layer. Considering that this species has a clutch size of a single egg, we found strong evidence of communal egg-laying in one site with 10 eggs close to each other; another three sites had two eggs each, and two eggs were found solitary in the leaf litter. Egg sites did not differ in temperature, humidity or leaf litter depth from random points without eggs along the quadrants. Fifteen of the 18 eggs hatched in the lab, with an average incubation time of 46.6 ± 18.5 days (range 15–73). In addition, an egg laid by a gravid female in the lab hatched after 65 days (relative clutch mass: 0.252). -
A New Genus of Miniaturized and Pug-Nosed Gecko from South America (Sphaerodactylidae: Gekkota)
Marquette University e-Publications@Marquette Biological Sciences Faculty Research and Publications Biological Sciences, Department of 12-2011 A New Genus of Miniaturized and Pug-Nosed Gecko from South America (Sphaerodactylidae: Gekkota) Tony Gamble Marquette University, [email protected] Juan D. Daza Villanova University Guarino R. Colli Universidade de Brasília Laurie J. Vitt University of Oklahoma Aaron M. Bauer Villanova University Follow this and additional works at: https://epublications.marquette.edu/bio_fac Part of the Biology Commons Recommended Citation Gamble, Tony; Daza, Juan D.; Colli, Guarino R.; Vitt, Laurie J.; and Bauer, Aaron M., "A New Genus of Miniaturized and Pug-Nosed Gecko from South America (Sphaerodactylidae: Gekkota)" (2011). Biological Sciences Faculty Research and Publications. 757. https://epublications.marquette.edu/bio_fac/757 Marquette University e-Publications@Marquette Biological Sciences Faculty Research and Publications/College of Arts and Sciences This paper is NOT THE PUBLISHED VERSION; but the author’s final, peer-reviewed manuscript. The published version may be accessed by following the link in the citation below. Zoological Journal of the Linnean Society, Vol. 163, No. 4 (December 2011) : 1244-1266. DOI. This article is © Oxford University Press and permission has been granted for this version to appear in e-Publications@Marquette. Oxford University Press does not grant permission for this article to be further copied/distributed or hosted elsewhere without the express permission from Oxford University Press. A New Genus of Miniaturized and Pug- Nosed Gecko from South America (Sphaerodactylidae: Gekkota) TONY GAMBLE Department of Genetics, Cell Biology and Development, University of Minnesota, Minneapolis, MN JUAN D. DAZA CONICET, Instituto de Herpetología, Fundación Miguel Lillo, San Miguel de Tucuman, Argentina Department of Biology, Villanova University, Villanova, PA GUARINO R. -
Aprasiainis87 FAMILY
61 GENUS: Oedura GENUS; Lygodactylus GENUS: Phyllurus GENUS: Matoatoa GENUS: Pseudothecadactyl us GENUS: Microscalabotes* GENUS: Rhacodactylus GENUS; Nactus GENUS: Rhynchoedura* GENUS: Narudasia* GENUS: SaItuarius GENUS: Pachydactylus GENUS: Underwoodisaurus GENUS; PaImatogecko SUBFAMILY: Eublepbarinae'" GENUS; Psragehyra GENUS: Coleonyx GENUS: Psroedura GENUS: Eublepbaris GENUS; Perochirus GENUS: Goniurosaurus GENUS: Phelsuma GENUS: Hemitheconyx GENUS: Phyllodactylus GENUS: Holodactylus GENUS; Phyllopezus SUBFAMILY: Gekkoninae GENUS: Pristurus GENUS: Afroedura GENUS; Pseudogekko GENUS: Afrogecko GENUS; Pseudogonatodes GENUS: Agamura GENUS: Plenopus GENUS: Ailuronyx GENUS: Plychozoon GENUS: Alsophylax GENUS; Plyodactylus GENUS; Arlstelliger GENUS: Quedenfeldtia GENUS; Asaccus GENUS: Rhoptropus GENUS; Blaesodactylus GENUS; Saurodactylus GENUS: Bogertia* GENUS: Sphaerodactylus GENUS; Brlha* GENUS; Stenodactylus GENUS: Bunopus GENUS; Tarentola GENUS: Calodactylodes GENUS; Teratolepis GENUS: Carinatogecko GENUS; Thecadactylus* GENUS: Chondrodactyiu,* GENUS: Tropiocoiotes GENUS; Christinus GENUS; Urocotyledon GENUS: Cnemaspis GENUS: Uroplatus GENUS; Coleodactylus SUBFAMILY: Teratoscincinae GENUS; Colopus* GENUS: Teratoscincus GENUS: Cosymbotus FAMILY: Pygopodidae'" GENUS: Crossobamon SUBFAMILY: LiaIisinae GENUS: Cryptactites' TRIBE: Aprasiaini S87 GENUS; Cyrtodactylus GENUS; J\prasia GENUS: Cyrtopodion GENUS: Ophidiocephalus* GENUS: Dixonius GENUS; Pletholax* GENUS: Dravidogecko* TRIBE: Lialisini GENUS; Ebenavia GENUS: LiaIis GENUS; EuIeptes* -
Arachnida: Araneae) Feeding on Snakes (Reptilia: Squamata
2021. Journal of Arachnology 49:1–27 INVITED REVIEW Spiders (Arachnida: Araneae) feeding on snakes (Reptilia: Squamata) Martin Nyffeler1 and J. Whitfield Gibbons2: 1Section of Conservation Biology, Department of Environmental Sciences, University of Basel, CH-4056 Basel, Switzerland. Email: [email protected] 2Odum School of Ecology, University of Georgia, Athens, GA 30602, USA Abstract. In this paper, 319 incidents of snake predation by spiders are reported based on a comprehensive global literature and social media survey. Snake-catching spiders have been documented from all continents except Antarctica. Snake predation by spiders has been most frequently documented in USA (51% of all incidents) and Australia (29%). The captured snakes are predominantly small-sized with an average body length of 25.9 6 1.3 cm (median ¼ 27 cm; range: 5.8–100 cm). Altogether .90 snake species from seven families have been documented to be captured by .40 spider species from 11 families. About 60% of the reported incidents were attributable to theridiids (’0.6–1.1 cm body length), a spider family that uses strong tangle webs for prey capture. Especially the Australian redback spider (Latrodectus hasselti Thorell, 1870), the African button spider (Latrodectus indistinctus O. Pickard-Cambridge, 1904), an Israeli widow spider (Latrodectus revivensis Shulov, 1948), and four species of North American widow spiders (Latrodectus geometricus C.L. Koch, 1841, Latrodectus hesperus Chamberlin & Ivie, 1935, Latrodectus mactans (Fabricius, 1775), and Latrodectus variolus Walckenaer, 1837) – equipped with a very potent vertebrate-specific toxin (a- latrotoxin) – have proven to be expert snake catchers. The use of vertebrates as a supplementary food source by spiders represents an opportunity to enlarge their food base, resulting in enhanced survival capability. -
Population Genetic Structure and Species Delimitation of a Widespread, Neotropical Dwarf Gecko Brendan J
Marquette University e-Publications@Marquette Biological Sciences Faculty Research and Biological Sciences, Department of Publications 4-1-2019 Population Genetic Structure and Species Delimitation of a Widespread, Neotropical Dwarf Gecko Brendan J. Pinto Marquette University Guarino R. Colli Universidade de Brasília Timothy E. Higham University of California - Riverside Anthony P. Russell University of Calgary Daniel P. Scantlebury Resonate, Reston, VA See next page for additional authors Accepted version. Molecular Phylogenetics and Evolution, Vol. 133 (April 2019): 54-66. DOI. © 2018 Elsevier Inc. Used with permission. Authors Brendan J. Pinto, Guarino R. Colli, Timothy E. Higham, Anthony P. Russell, Daniel P. Scantlebury, Laurie J. Vitt, and Tony Gamble This article is available at e-Publications@Marquette: https://epublications.marquette.edu/bio_fac/675 Marquette University e-Publications@Marquette Biology Faculty Research and Publications/College of Arts and Sciences This paper is NOT THE PUBLISHED VERSION; but the author’s final, peer-reviewed manuscript. The published version may be accessed by following the link in th citation below. Molecular Phylogenetics and Evolution, Vol. 133 (April 2019): 54-66. DOI. This article is © Elsevier and permission has been granted for this version to appear in e-Publications@Marquette. Elsevier does not grant permission for this article to be further copied/distributed or hosted elsewhere without the express permission from Elsevier. Population genetic structure and species delimitation of a widespread, Neotropical dwarf gecko Brendan J. Pinto Department of Biological Sciences, Marquette University, Milwaukee, WI, USA Guarino R. Colli Departamento de Zoologia, Universidade de Brasília, Brasília, DF, Brazil Timothy E. Higham Department of Evolution, Ecology, and Organismal Biology, University of California, Riverside, Riverside, CA, USA Anthony P.