92 IRCF Reptiles & Amphibians • Vol 18, No 2 • Jun 2011 Young Aruba
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Predation on Ameiva Ameiva (Squamata: Teiidae) by Ardea Alba (Pelecaniformes: Ardeidae) in the Southwestern Brazilian Amazon
Herpetology Notes, volume 14: 1073-1075 (2021) (published online on 10 August 2021) Predation on Ameiva ameiva (Squamata: Teiidae) by Ardea alba (Pelecaniformes: Ardeidae) in the southwestern Brazilian Amazon Raul A. Pommer-Barbosa1,*, Alisson M. Albino2, Jessica F.T. Reis3, and Saara N. Fialho4 Lizards and frogs are eaten by a wide range of wetlands, being found mainly in lakes, wetlands, predators and are a food source for many bird species flooded areas, rivers, dams, mangroves, swamps, in neotropical forests (Poulin et al., 2001). However, and the shallow waters of salt lakes. It is a species predation events are poorly observed in nature and of diurnal feeding habits, but its activity peak occurs hardly documented (e.g., Malkmus, 2000; Aguiar and either at dawn or dusk. This characteristic changes Di-Bernardo, 2004; Silva et al., 2021). Such records in coastal environments, where its feeding habit is are certainly very rare for the teiid lizard Ameiva linked to the tides (McCrimmon et al., 2020). Its diet ameiva (Linnaeus, 1758) (Maffei et al., 2007). is varied and may include amphibians, snakes, insects, Found in most parts of Brazil, A. ameiva is commonly fish, aquatic larvae, mollusks, small crustaceans, small known as Amazon Racerunner or Giant Ameiva, and birds, small mammals, and lizards (Martínez-Vilalta, it has one of the widest geographical distributions 1992; Miranda and Collazo, 1997; Figueroa and among neotropical lizards. It occurs in open areas all Corales Stappung, 2003; Kushlan and Hancock 2005). over South America, the Galapagos Islands (Vanzolini We here report a predation event on the Ameiva ameiva et al., 1980), Panama, and several Caribbean islands by Ardea alba in the southwestern Brazilian Amazon. -
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. -
Helminths from Lizards (Reptilia: Squamata) at the Cerrado of Goiás State, Brazil Author(S): Robson W
Helminths from Lizards (Reptilia: Squamata) at the Cerrado of Goiás State, Brazil Author(s): Robson W. Ávila, Manoela W. Cardoso, Fabrício H. Oda, and Reinaldo J. da Silva Source: Comparative Parasitology, 78(1):120-128. 2011. Published By: The Helminthological Society of Washington DOI: 10.1654/4472.1 URL: http://www.bioone.org/doi/full/10.1654/4472.1 BioOne (www.bioone.org) is an electronic aggregator of bioscience research content, and the online home to over 160 journals and books published by not-for-profit societies, associations, museums, institutions, and presses. Your use of this PDF, the BioOne Web site, and all posted and associated content indicates your acceptance of BioOne’s Terms of Use, available at www.bioone.org/page/terms_of_use. Usage of BioOne content is strictly limited to personal, educational, and non-commercial use. Commercial inquiries or rights and permissions requests should be directed to the individual publisher as copyright holder. BioOne sees sustainable scholarly publishing as an inherently collaborative enterprise connecting authors, nonprofit publishers, academic institutions, research libraries, and research funders in the common goal of maximizing access to critical research. Comp. Parasitol. 78(1), 2011, pp. 120–128 Helminths from Lizards (Reptilia: Squamata) at the Cerrado of Goia´s State, Brazil 1,4 2 3 1 ROBSON W. A´ VILA, MANOELA W. CARDOSO, FABRI´CIO H. ODA, AND REINALDO J. DA SILVA 1 Departamento de Parasitologia, Instituto de Biocieˆncias, UNESP, Distrito de Rubia˜o Jr., CEP 18618-000, Botucatu, SP, Brazil, 2 Departamento de Vertebrados, Museu Nacional, Universidade Federal do Rio de Janeiro, Quinta da Boa Vista, CEP 20940- 040, Rio de Janeiro, RJ, Brazil, and 3 Universidade Federal de Goia´s–UFG, Laborato´rio de Comportamento Animal, Instituto de Cieˆncias Biolo´gicas, Campus Samambaia, Conjunto Itatiaia, CEP 74000-970. -
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). -
Lac Bay: Then and Now… a Historical Interpretation of Environmental Change During the 1900S
Lac Bay: Then and Now… A Historical Interpretation of Environmental Change During the 1900s A Site Characterization of Lac Bay for Resource Managers and Naturalists prepared for Bonaire Marine Park by Environics, N.V. Cynthia E. Lott, Environmental Consultant Final Edition October 2001 Lac Bay Then and Now A Historical Interpretation of Environmental Change During the 1900s A Site Characterization of Lac Bay For Resource Managers and Naturalists By Cynthia E. Lott Environmental Consultant Bonaire, Netherlands Antilles Final Edition October 2001 Copyright 2001 All rights reserved Title Page Map Credits: Top: Year 1866, Year 1911 (Hummelinck en Roos 1969); Middle: Year 1949, Year 1967 (Hummelinck en Roos 1969); Bottom left: Year 1961 (Hummelinck en Roos 1969); Bottom right: Year 1998 (Wing Group, N.V. 1998/Dec.) This Work is dedicated… In the fondest memory of My beloved friend, Dick Harrison, who encouraged me to believe in myself. God Bless Us Every One…. Lac Bay: Then and Now…A Historical Interpretation of Environmental Change During the 1900s A Site Characterization for Resource Managers and Naturalists Foreword by Boi Antoin, Editor of EXTRA, Bonaire's Daily Newspaper, and respected local historian LAC No tin duda ku Lac ta un sitio, un bahia, ku nos mester trata na protehá i konservá na tur manera. E historia, kultura i naturalesa di Lac hamas por bai pèrdí. Asina importante e lugá aki tabata I ta pa Boneiru. Despues di investigashonnan arkeológiko i ekológiko ku a tuma lugá di Lac, tabata nesesario, na mi konsepto, pa a bini ku un investigashon mas profundo i sientífiko di e área bunita aki. -
FOOD HABITS of the LIZARD Ameiva Ameiva (LINNAEUS, 1758) (SAURIA: TEIIDAE) in a TROPOPHIC FOREST of SUCRE STATE, VENEZUELA
Acta Biol. Venez.Vol. 28 (2): 53-59. Junio-Diciembre, 2008 FOOD HABITS OF THE LIZARD Ameiva ameiva (LINNAEUS, 1758) (SAURIA: TEIIDAE) IN A TROPOPHIC FOREST OF SUCRE STATE, VENEZUELA. HÁBITOS ALIMENTARIOS DEL LAGARTO Ameiva ameiva (LINNAEUS, 1758) (SAURIA: TEIIDAE) EN UN BOSQUE TROPÓFILO DEL ESTADO SUCRE, VENEZUELA. Luis Alejandro González S. 1-2, Jenniffer Velásquez2, Hernán Ferrer3, James García1, Francia Cala1 and José Peñuela1 1- Departamento de Biología, Laboratorio de Ecología Animal, Universidad de Oriente, Cumaná, Venezuela. ([email protected]); 2. Posgrado de Zoología, Instituto de Zoología Tropical, Facultad de Ciencias, Universidad Central de Venezuela ([email protected]); 3. Gerencia de Investigación y Desarrollo, Jardín Botánico de Caracas, Universidad Central de Venezuela, Caracas, Venezuela ([email protected]). ABSTRACT Food habits among sexes of Ameiva ameiva were evaluated by the frequency of occurrence, trophic dominance, and diet similarity methods during periods of rain and drought in a tropophic forest in La Llanada Vieja, Sucre State, Venezuela. 431 prey items were identified in 20 stomachs analyzed. Diet for both periods showed a high frequency for Coleoptera, plant material, Isoptera, Nematoda, Araneae, and reptilian rests. Males and females showed differences in diet during the climatic periods analyzed. Females showed higher stomach volumes values than males. Results suggest the species is mainly insectivorous. RESUMEN Se evaluaron los hábitos alimentarios de Ameiva ameiva, mediante el método de frecuencia de aparición, dominancia trófica y similitud de la dieta entre sexos, abarcando los periodos de lluvia y sequía. La captura se realizó en un bosque tropófilo de los alrededores de la Llanada Vieja, estado Sucre, Venezuela. -
The Bisexual Brain: Sex Behavior Differences and Sex Differences in Parthenogenetic and Sexual Lizards
BRAIN RESEARCH ELSEVIER Brain Research 663 (1994) 163-167 Short communication The bisexual brain: sex behavior differences and sex differences in parthenogenetic and sexual lizards Matthew S. Rand *, David Crews Institute of Reproductive Biology, Department of Zoology, University of Texas at Austin, Austin, TX 78712, USA Accepted 2 August 1994 Abstract The parthenogenetic lizard Cnemidophorus uniparens alternates in the display of male-like and female-like sexual behavior, providing a unique opportunity for determining the neuronal circuits subserving gender-typical sexual behavior within a single sex. Here we report a 6-fold greater [14C]2-fluoro-2-deoxyglucose uptake in the medial preoptic area of C. uniparens displaying male-like behavior in comparison with C. uniparens displaying female-like receptivity. The ventromedial nucleus of the hypothalamus showed greater 2DG accumulation in receptive C. uniparens than in courting C. uniparens. When a related sexual species (C. inornatus) was compared to the unisexual species, the anterior hypothalamus in C. inornatus males exhibited significantly greater activity. Keywords: 2-Deoxyglucose; Anterior hypothalamus; Medial preoptic area; Reptile; Ventromedial hypothalamus Female-typical and male-typical sex behavior are C. inornatus [7,17]. The aims of this study were to known to be integrated by specific hypothalamic nuclei determine: (1) if specific regions in the brains of in the vertebrate brain [6,18,22]. The ventromedial parthenogenetic and gonochoristic whiptail lizards ex- nucleus of the hypothalamus (VMH) and the medial hibit sexually dimorphic metabolic activity, as mea- preoptic area (mPOA) are involved in sexual receptiv- sured by the accumulation of [14C]2-fluoro-2-de- ity in females and both the mPOA and anterior hy- oxyglucose (2DG) in the brain during mating behavior, pothalamus (AH) play an important role in the regula- and (2) if these dimorphisms complement previous tion of copulatory behavior in males [6,18,19,22]. -
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. -
Endoparasites Infecting Two Species of Whiptail Lizard (<I
SHORT NOTES SHORT NOTES 1980; Ribas et al., 1995; 1998; Vrcibradic et al., 2000; Menezes et al., 2004). In this study we survey the en- doparasite faunas of two sympatric species of whiptail HERPETOLOGICAL JOURNAL, Vol. 15, pp. 133-137 (2005) lizards from Brazil, Cnemidophorus abaetensis Dias, ENDOPARASITES INFECTING TWO Rocha & Vrcibradic, 2002 and Cnemidophorus ocellifer (Spix, 1824). Cnemidophorus abaetensis is a recently SPECIES OF WHIPTAIL LIZARD described species whose geographic distribution is ap- (CNEMIDOPHORUS ABAETENSIS AND parently restricted to the northern coast of Bahia state C. OCELLIFER; TEIIDAE) IN A (Dias et al., 2002), whereas C. ocellifer is widespread in ‘RESTINGA’ HABITAT OF NORTH- South America south of the Amazonian region, from EASTERN BRAZIL north-eastern and central Brazil to Paraguay, Bolivia and northern Argentina (Vanzolini et al., 1980; Cei, EDUARDO JOSÉ R. DIAS, DAVOR VRCIBRADIC 1993). So far, nothing has been published about the AND CARLOS FREDERICO D. ROCHA endoparasites associated with these two species [in the study of Ribas et al., (1995) regarding nematodes of C. Setor de Ecologia, Instituto de Biologia, Universidade do ocellifer, the species under treatment is actually C. Estado do Rio de Janeiro, Rua São Francisco Xavier littoralis Rocha, Araújo, Vrcibradic & Costa, 2000, 524, 20550-011, Rio de Janeiro, RJ, Brazil which had not yet been formally described at the time We analysed the endoparasite fauna associated with (see Rocha et al., 2000a)]. two species of whiptail lizard (Cnemidophorus A total of 73 lizards (33 C. abaetensis and 40 C. abaetensis and C. ocellifer) from north-eastern Brazil. ocellifer) were collected by the first author with the aid Overall parasite prevalence was relatively low for both of elastic rubber bands at the coastal sand-dune species (18.2% in C. -
Ameiva Ameiva (Zandolie Or Jungle Runner)
UWI The Online Guide to the Animals of Trinidad and Tobago Ecology Ameiva ameiva (Zandolie or Jungle Runner) Family: Teiidae (Tegus and Whiptails) Order: Squamata (Lizards and Snakes) Class: Reptilia (Reptiles) Fig. 1. Zandolie, Ameiva ameiva. [https://c2.staticflickr.com/4/3804/13311081294_c5a2cfcfc8_b.jpg, downloaded 29 March 2015] TRAITS. Ameiva ameiva lizards are large bodied, streamlined in shape, their heads are pointed and their tongues are slightly forked. Their legs are short and their hind legs are very muscular (Fig. 1). These lizards display sexual dimorphism. The female body length is approximately 49cm and the male 56 cm (ttfnc.org, 2006). The males are larger than the females in size, their backs are dull green and their flanks are colourful, whereas the females are quite similar but they have much brighter green backs (Kenny, 2008). The males also have relatively larger heads than the females (Colli and Vitt, 1994). Juveniles have relatively large heads for their body size. Ameiva ameiva is also called the jungle runner or giant ameiva (Myfwc.com, 2015). DISTRIBUTION. According to Animal Diversity Web (2014), Ameiva ameiva is found in Central and South America and in some parts of the Caribbean. Countries include; Brazil, Panama, Trinidad and Tobago, Suriname, Colombia and many others. UWI The Online Guide to the Animals of Trinidad and Tobago Ecology HABITAT AND ACTIVITY. They are diurnal, found in open tropical forests, woodlands and agricultural land (Anapsid.org, 1995), in open, sunny, grassy areas. Biazquez (1996) says that both adults and juveniles liked sunny areas and they spend most of their time foraging and basking. -
Range Extension and Geographic Distribution of the Poorly Known Species, Contomastix Leachei Peracca, 1897
Check List 9(4): 844–846, 2013 © 2013 Check List and Authors Chec List ISSN 1809-127X (available at www.checklist.org.br) Journal of species lists and distribution N Range extension and geographic distribution of the poorly known species, Contomastix leachei Peracca, 1897 ISTRIBUTIO (Squamata: Teiidae) D 1,2* 1 1 RAPHIC Federico José Arias , Francisco Barrios and Antonio Palavecino G EO G 1 Universidad Nacional de Salta, Instituto de Bio y Geociencias del Noa (IBIGEO). Avenida Bolivia 5150, Salta 4400, Argentina.. N 2 Universidade de São Paulo, Instituto de Biociências, Departamento de Zoologia, Caixa Postal 11.46 1, CEP 05422-970, São Paulo, Brazil. O * Corresponding author. E-mail: [email protected] OTES N Abstract: The records of distribution of Contomastix leachei Peracca, 1897 indicate that this species is endemic of Southeast Jujuy Province, occurring only in the Ledesma Department. Here, we report the southernmost known locality of this species, from Alemanía, Salta Province, Argentina. This record represents the southern limit of distribution of the species. We also provide an updated range map for this species based on data from museum records and field studies. The Contomastix genus was recently proposed by transition”, which is characterized by being drier than the Harvey et al. (2012) for grouping the species of the “Yungas sensu stricto”, with vegetation typical of the semi- formerly called Cnemidophorus lacertoides group (Cei arid Chaco and “Chaco serrano” ecotones (Brown et al. 1993) in a monophyletic cluster. Five species are currently 2002). recognized for this new genus: C. lacertoides, C. leachei, In order to evaluate the taxonomic status of the C. -
Mjie,Ianjfuseum
MJie,ianJfuseum PUBLISHED BY THE AMERICAN MUSEUM OF NATURAL HISTORY CENTRAL PARK WEST AT 79TH STREET, NEW YORK 24, N.Y. NUMBER 1934 APRIL 22, 1959 Taxonomic Notes on a Collection of Venezuelan Reptiles in the American Museum of Natural History BY JANIS A. ROZE1 INTRODUCTION While visiting museums2 in the United States in an effort to prepare a monographic study of the Venezuelan snake fauna, I had the privi- lege of examining an unidentified reptile collection in the American Museum of Natural History. It contained 72 specimens, representing 25 species and subspecies, two of which proved to be undescribed. Notes on specimens from the United States National Museum (U.S.N.M.), Carnegie Museum, Pittsburgh (C.M.), and Museo de Biologia, Univer- sidad Central de Venezuela, Caracas, Venezuela (M.B.U.C.V.), are added. At present the state of our knowledge concerning the systematic position of the amphibians and reptiles, or, indeed, the flora and fauna, of South America in general and Venezuela in particular leaves much to be desired. The situation here is similar to the one existing about 50 to 70 years ago in Europe or North America; thus every speci- men collected contributes to our understanding of the various popula- tions within a given area, or discloses the existence of taxa not pre- ' Escuela de Biologia, Universidad Central de Venezuela. 2 The trip was financed by the Fundaci6n Creole, Caracas, Venezuela, and the Council Research Fund of the American Museum of Natural History. 2 AMERICAN MUSEUM NOVITATES NO. 1934 viously recognized. Not until rather exhaustive taxonomic studies have been completed can the zoogeographical and ecological problems be fully appreciated and worked out in detail.