(Lazell, 1989; Bartlett and Bartlett, 1999A). Devel

Total Page:16

File Type:pdf, Size:1020Kb

(Lazell, 1989; Bartlett and Bartlett, 1999A). Devel young hatch as miniature froglets (Lazell, animals ate numerous ants, mites, spiders, Villa, 1972; Meyer and Foster, 1996; Lev- 1989; Bartlett and Bartlett, 1999a). Devel- and longlegs (Stewart, 1979). ell, 1997; McCranie and Wilson, 2002). opment may be accelerated by warmer 0.Predators. In the Everglades, green- temperatures, with hatching occurring as house frogs are eaten by Cuban treefrogs 1. Historical versus Current Distribution. early as 13 d post-deposition (Lazell, (Osteopilus septentrionalis) and ring-necked White-lipped frogs (Leptodactylus bgilis) 1989). Lazell (1989) notes that hatching snakes (Dindophis punctatus; Wilson and are known throughout lowland Middle appears to be most successful with 100% Porras, 1983; Meshaka, 1994, 2001; Me- America to the north coast of South Amer- humidity. shaka et al., 2004). ica as far as Venezuela (Heyer, 1978,2002). i. Brood sltes. Eggs are laid on the P. Anti-Predator Mechanisms. Unknown. In the United States, these frogs margin- ground under moist cover (Lazell, 1989), a. Diseases. Unknown. ally occur in southernmost Texas, specifi- but females are not known to brood R. Parasites. None reported in the cally in the extreme southern edge of the (Goin, 1947a). United States. Lower Rio Grande Valley (Garrett and li. Parental care. None (Goin, 1947a). Barker, 1987). They are known historically D. Juvenile Habitat. Humid areas that 4. Conservation. from one locality in Cameron County, provide cover, such as leaf mold, flower Greenhouse frog populations appear to be two localities in Hidalgo County, and one beds, and moist litter (Goin, 1947a; Carr stable across much of their native range. locality from Starr County (Heyer, 1978). and Goin, 1955). They have been rapidly expanding their Dixon (1987, 1996) reported no new lo- E. Adult Habitat. Same as juveniles; distribution up peninsular Florida and calities. adults are found in humid habitats that along the Gulf Coast and have been intro- provide cover (Carr, 1940a). Greenhouse duced in Hawaii on Hawaii Island and 2. Historical versus Current Abundance. frogs are particularly common in gardens, Oahu, where they are considered an inva- Dixon (1987, p. 66) commented: "This greenhouses, nurseries, and other moist sive species (Bartlett and Bartlett, 1999a; frog may be extirpated from Texas substrates (Goin, 1944; Bartlett and Kraus et al., 1999; Meshaka et al., 2004; through the continuous dispersal of Bartlett, 1999a). These frogs will hide be- M. Stewart, personal communication). organophosphate chemicals in the Rio neath leaf litter, mulch, boards, or step- Greenhouse frogs are locally abundant Grande Valley." ping stones (Carr, 1940a; Bartlett and and occur across a wide range of habitats Bartlett, 1999a). Greenhouse frogs are also and regions in Florida (Carr, 1940a; Dal- 3. Life History Features. found outside of human influence in suit- rymple, 1988; Lips, 1991; Meshaka et al., A. Breeding. able natural habitats (Buttertield et al., 2000). In this connection, greenhouse i. Breeding migrations. Males have been 1997). They are secretive and nocturnal frogs have the potential to compete for found calling under clumps of grass, dirt except on warm, overcast, or rainy days food with lizards such as reef geckos clods, and from small depressions (Garrett (Carr, 1940a; Bartlett and Bartlett, 1999a). (Sphaerodactylus notatus) and mole skinks and Barker, 1987). F. Home Range Size. Unknown. (Eumeces egregius), which are already li. Breeding habitat. Brooding chambers, G. Territories. Unknown. threatened because they are habitat spe- excavated by males, are found under H. Aestivation/Avoiding Desiccation. Un- cialists and their habitat is rapidly disap- rocks, logs, or debris in clay soil (Dixon known. pearing. and Heyer, 1968). Dixon and Heyer (1968) I. Seasonal Migrations. None. note that these chambers may contain calling males or foam nests. J. Torpor (Hibernation). In late March in Leptodactylus fragilis Brocchi, 1877 B. Eggs. the southern Everglades of Florida, green- WHITE-LIPPED FROG house frogs have been found hibernating i. Egg deposition s~tes.Eggs are laid in W. Ronald Heyer underneath the loose bark of wild foam nests, created by. body. secretions, in tamarind (Lysiloma sp.), a small tree com- Author's note: Leptodactylus fragilis has small brooding chambers excavated by mon in the hammocks (Harper, 1935). been cited historically as either L. albi- adults (Maslin, 1963a,b; Garrett and K. lnterspecific Associations/Exclusions. labris (e.g., Metcalf, 1923, in part) or L. Barker, 1987).The foam aids in preventing Greenhouse frogs are found under the labialis (e.g., Mulaik, 1937; Maslin, 1963a,b; desiccation of the eggs during develop- same cover objects as eastern narrow- Dixon and Heyer, 1968; Heyer, 1971; ment (Garrett and Barker, 1987). mouthed toads (Gastrophryne carolinensis; Carr, 1940a; personal observations) and in the same habitats as many small fossorial and semi-fossorial amphibians and rep- White-lipped Frog (Leptodactylus fragilis) I tiles (Dalrymple, 1988; Conant and Collins, 1998; Meshaka et al., 2000; Me- shaka and Layne, 2002,2005), with which they may or may not compete. L. Age/Size at Reproductive Maturity. Sexually mature male greenhouse frogs range in size from 15.0-17.5 mm SVL; fe- males range from 19.5-25.0 mm SVL (Bartlett and Bartlett, 1999a). Lazell (1989) records a large adult measuring 32 mm. Sexual maturity is reached in 1 yr (Goin, 1947a; Duellman and Schwartz, 1958). M. Longevity. Unknown. N. Feeding Behavior. In order of occur- rence, greenhouse frogs eat ants, beetles, and roaches, but include other types of small invertebrates (Goin, 1947a; Duell- man and Schwartz, 1958; Lazell, 1989). In Jamaica, diet did not include roaches, but -- - ---- 11. Clutch s~ze-Afoam nest from Texas County (Heyer, 1978; see above). Dixa_n_- gles, 1952; B1ane~-1971; Gibbons and contained 86 yellow eggs_&iulaik, 1937). (1987, 1996) reported nmgities Coker,_l918; Braswell, 1988; Learm et al., Villa (1972, p. 122) reported 25-250 eggs/ and comments (1987, p. 66) "This frog 1999). Th-nct population In south- - - nest. may be extirpated from Texas through the eastern Iowa may be extirpated (Klimstra, C. Larvae/Metamorphosis. Early devel- continuous dispersal of organophosphate 1950; Nelson, 1972~). opment takes place in the foam nests chemicals in the Rio Grande Valley." within the brooding chamber; larvae are McCranie and Wilson (2002, p. 533) released to ponds during heavy rains state that white-lipped frogs are of low 2. Historicalversus Current Abundance. (Dixon and Ileyer, 1968). vulnerability in at least parts of their dis- Eastern narrow-mouthed toads are soli- tary, secretive, and common throughout I. Length of larval stage. Mulaik (1937) tribution. reported a larval duration of 30-35 d in a Alabama (Mount, 1975), Florida (Carr, Texas population. Meyer and Foster (1996) 1940a), and Louisiana (Penn, 1943; An- state that in Belize the tadpoles usually Family Microhylidae derson, 1954), and locally common in Illi- metamorphose in <2 wk. nois (Phillips et al., 2000) and Virginia Gastrophryne carolinensis (Holbrook, 1836) (Hoffman and Mitchell, 1996). Eastern 11. Larval requirements. Unknown. EASTERN NARROW-MOUTHED TOAD 11i.Larval polymorph~sms.None. narrow-mouthed toads are commonly Joseph C. Mitchell, Michael J. Lannoo captured in drift fences with pitfall traps IV. Features of metamorphos~s.See ''Length of larval stage" above. (Gibbons and Bennett, 1974; Buhlmann v. Post-metamorphic mlgratlons. Unknown. 1. Historical versus Current Distribution. et al., 1994; Enge, 1997). Some studies D. Juvenile Habitat. Likely the same as Eastern narrow-mouthed toads (Gas- have revealed large numbers in local pop- adults. trophryne carolinensis) occur in the south- ulations (e.g., Bennett et al., 1980; Gib- E. Adult Habitat. Adult white-lipped eastern and lower midwestern United bons and Semlitsch, 1981; Dodd, 1992, frogs have been found in a variety of habi- States, from Maryland south to the Florida 1995b), although annual variation in tats where moisture is sufficient (Garrett Keys, west to central Texas, and north to numbers encountered varies among sites and Barker, 1987). These frogs can be Kentucky, southern Illinois, southern Mis- and years (Dodd, 1995b; Semlitsch et al., found in semi-permanent water bodies souri, and extreme southeastern Nebraska 1996; Enge, 1997). such as prairie potholes, oxbow lakes, and (Carr, 1940a; Wright and Wright, 1949; Abundance estimates or counts are resacas (Edwards et al., 1989). Garrett and Duellman and Schwartz, 1958; Nelson, highly dependent on the sampling tech- Barker (1987) note that white-lipped frogs 1972c; Harris, 1975; Martof et al., 1980; nique used. Funnel traps along drift fences may be encountered in irrigated agricul- Ashton and Ashton, 1988; Dundee and revealed few individuals in a study in tural fields, Irrigation ditches, low grass- Rossman, 1989; Conant and Collins, northern Florida (Vickers et al., 1985). lands, and runoff areas. These frogs are 1991; Redmond and Scott, 1996; Bartlett Lamb et al. (1998) reported only 19 east- nocturnally active and may hide in bur- and Bartlett, 1999a; Mitchell and Reay, ern narrow-mouthed toads among 1,070 rows during the day (Garrett and Barker, 1999; Phillips et al., 1999; Dixon, 2000; frogs encountered under coverboards in a 1987). Johnson, 2000). Minton (2001) specu- North Carolina floodplain. Coverboards F. Home Range Size. Unknown. lated that this anuran may occur in Indi- in South Carolina produced few captures, G. Territories. Males call in association ana. They reach elevations to 549 m in the whereas drift fences with pitfall traps with incubating chambers (Dixon and Smoky Mountains National Park (Huheey yielded thousands of captures over the Heyer, 1968) and would be expected to de- and Stupka, 1967), although they are ab- same time period (Grant et al., 1992). fend these sites from other males, al- sent from most of the Blue Ridge Moun- However, Grant et al. (1994) recorded though this has yet to be documented. tains and the Appalachian region north of high numbers of narrow-mouthed toads H. Aestivation/Avoiding Desiccation. Un- Tennessee (Redmond and Scott, 1996).
Recommended publications
  • Herpetological Journal FULL PAPER
    Volume 26 (January 2017), 73–80 Herpetological Journal FULL PAPER Published by the British Herpetological Society Reproductive biology of the nest building vizcacheras frog Leptodactylus bufonius (Amphibia, Anura, Leptodactylidae), including a description of unusual courtship behaviour Gabriel Faggioni1, Franco Souza1, Masao Uetanabaro1, Paulo Landgref-Filho2, Joe Furman3 & Cynthia Prado1,4 1Programa de Pós-Graduação em Ecologia e Conservação, Universidade Federal de Mato Grosso do Sul, Campo Grande, Brasil 2Campo Grande, Brasil 3Houston, USA 4Departamento de Morfologia e Fisiologia Animal, Universidade Estadual Paulista, Jaboticabal, Brasil We describe the reproductive biology and sexual size dimorphism of a population of the vizcacheras frog Leptodactylus bufonius in the Brazilian Chaco. Reproduction takes place during the rainy months (September–March). During courtship, females emit reciprocal calls and both sexes perform vibratory movements of the body; the latter is described for the first time in anurans. Amplexus and oviposition occurred inside subterranean chambers. The temperature in closed chambers was lower than outside chambers, which may aid in reducing desiccation risks of eggs and tadpoles. Females were larger than males, but males had longer heads and shorter tibias, which may be related to digging. The study reinforces the importance of ongoing discoveries on anuran natural history. Keywords: Chaco, natural history, sexual size dimorphism, subterranean chamber, vibratory movements INTRODUCTION 1988; Haddad & Giaretta, 1999; Haddad & Sawaya, 2000; Lucas et al., 2008; Kokubum et al., 2009). he genus Leptodactylus Fitzinger, 1826, comprises 74 Species in the L. fuscus group reproduce in sub- species distributed from southern Texas to Argentina, terranean chambers which may vary in size, shape, includingT Caribbean islands (Frost, 2015).
    [Show full text]
  • Chec List a Checklist of the Amphibians and Reptiles of San
    Check List 10(4): 870–877, 2014 © 2014 Check List and Authors Chec List ISSN 1809-127X (available at www.checklist.org.br) Journal of species lists and distribution PECIES S OF A checklist * of the amphibians and reptiles of San Isidro de ISTS L Dota, Reserva Forestal Los Santos, Costa Rica Erick Arias and Federico Bolaños [email protected] Universidad de Costa Rica, Escuela de Biología, Museo de Zoología. San Pedro, 11501-2060, San José, Costa Rica. * Corresponding author. E-mail: Abstract: We present an inventory of amphibians and reptiles of San Isidro de Dota, northwest of the Cordillera de Talamanca in the Central Pacific of Costa Rica.Leptodactylus The study was insularum conduced from January to August 2012 in premontane wet Coloptychonforest from 689 rhombifer m to 800 m elevation. We found a total of 56 species, including 30 species of amphibians and 26 of reptiles. It results striking the presence of the frog , uncommon above 400 m elevation, and the lizard , a very uncommon species. DOI: 10.15560/10.4.870 Introduction datum, from 689 m to 800 N, 83°58′32.41″ W, WGS84et al. Lower Central America represents one of the regions m elevation). The region is dominated by premontane with the highest numberet al of amphibianset describedal. in the wet forest (Bolaños 1999) with several sites used Neotropics in relation to the area it represent (Savage for agriculture and pastures. The region presents the 2002; Boza-Oviedo . 2012; Hertz 2012). Much climate of the pacific slope of the Cordillera de Talamanca, of this richness of species iset associated al.
    [Show full text]
  • Draft Environmental Assessment for the Rio Grande City Station Road
    DRAFT FINDING OF NO SIGNIFIGANT IMPACT (FONSI) RIO GRANDE CITY STATION ROAD IMPROVEMENT PROJECT, RIO GRANDE CITY, TEXAS, RIO GRANDE VALLEY SECTOR, U.S. CUSTOMS AND BORDER PROTECTION DEPARTMENT OF HOMELAND SECURITY U.S. BORDER PATROL, RIO GRANDE VALLEY SECTOR, TEXAS U.S. CUSTOMS AND BORDER PROTECTION DEPARTMENT OF HOMELAND SECURITY WASHINGTON, D.C. INTRODUCTION: United States (U.S.) Customs and Border Protection (CBP) plans to upgrade and lengthen four existing roads in the U.S. Border Patrol (USBP) Rio Grande City (RGC) Station’s Area of Responsibility (AOR). The Border Patrol Air and Marine Program Management Office (BPAM-PMO) within CBP has prepared an Environmental Assessment (EA). This EA addresses the proposed upgrade and construction of the four aforementioned roads and the BPAM-PMO is preparing this EA on behalf of the USBP Headquarters. CBP is the law enforcement component of the U.S. Department of Homeland Security (DHS) that is responsible for securing the border and facilitating lawful international trade and travel. USBP is the uniformed law enforcement subcomponent of CBP responsible for patrolling and securing the border between the land ports of entry. PROJECT LOCATION: The roads are located within the RGC Station’s AOR, Rio Grande Valley (RGV) Sector, in Starr County, Texas. The RGC Station’s AOR encompasses approximately 1,228 square miles, including approximately 68 miles along the U.S.-Mexico border and the Rio Grande from the Starr/Zapata County line to the Starr/Hidalgo County line. From north to south, the four road segments are named Mouth of River to Chapeno Hard Top, Chapeno USIBWC Gate to Salineno, Salineno to Enron, and 19-20 Area to Fronton Fishing, and all of these segments are located south of Falcon International Reservoir (Falcon Lake), generally parallel to the Rio Grande.
    [Show full text]
  • Leptodactylus Bufonius Sally Positioned. the Oral Disc Is Ventrally
    905.1 AMPHIBIA: ANURA: LEPTODACTYLIDAE Leptodactylus bufonius Catalogue of American Amphibians and Reptiles. Schalk, C. M. and D. J. Leavitt. 2017. Leptodactylus bufonius. Leptodactylus bufonius Boulenger Oven Frog Leptodactylus bufonius Boulenger 1894a: 348. Type locality, “Asunción, Paraguay.” Lectotype, designated by Heyer (1978), Museum of Natural History (BMNH) Figure 1. Calling male Leptodactylus bufonius 1947.2.17.72, an adult female collected in Cordillera, Santa Cruz, Bolivia. Photograph by by G.A. Boulenger (not examined by au- Christopher M. Schalk. thors). See Remarks. Leptodactylus bufonis Vogel, 1963: 100. Lap- sus. sally positioned. Te oral disc is ventrally po- CONTENT. No subspecies are recognized. sitioned. Te tooth row formula is 2(2)/3(1). Te oral disc is slightly emarginated, sur- DESCRIPTION. Leptodactylus bufonius rounded with marginal papillae, and possess- is a moderately-sized species of the genus es a dorsal gap. A row of submarginal papil- (following criteria established by Heyer and lae is present. Te spiracle is sinistral and the Tompson [2000]) with adult snout-vent vent tube is median. Te tail fns originate at length (SVL) ranging between 44–62 mm the tail-body junction. Te tail fns are trans- (Table 1). Head width is generally greater parent, almost unspotted (Cei 1980). Indi- than head length and hind limbs are moder- viduals collected from the Bolivian Chaco ately short (Table 1). Leptodactylus bufonius possessed tail fns that were darkly pigment- lacks distinct dorsolateral folds. Te tarsus ed with melanophores, especially towards contains white tubercles, but the sole of the the terminal end of the tail (Christopher M. foot is usually smooth.
    [Show full text]
  • Cfreptiles & Amphibians
    HTTPS://JOURNALS.KU.EDU/REPTILESANDAMPHIBIANSTABLE OF CONTENTS IRCF REPTILES & AMPHIBIANSREPTILES • VOL15, & N AMPHIBIANSO 4 • DEC 2008 •189 28(1):98–99 • APR 2021 IRCF REPTILES & AMPHIBIANS CONSERVATION AND NATURAL HISTORY TABLE OF CONTENTS FEATUREPredation ARTICLES on a Middle American . Chasing Bullsnakes (Pituophis catenifer sayi) in Wisconsin: White-lippedOn the Road to Understanding the Ecology Frog and Conservation (Leptodactylus of the Midwest’s Giant Serpent ...................... Joshua fragilis M. Kapfer 190 ) . The Shared History of Treeboas (Corallus grenadensis) and Humans on Grenada: (Anura:Leptodactylidae)A Hypothetical Excursion ............................................................................................................................ by a CaribbeanRobert W. Henderson 198 RESEARCH ARTICLES . DitchfrogThe Texas Horned Lizard in Central and( WesternLeptodactylus Texas ....................... Emily Henry, Jason Brewer, insularum Krista Mougey, and Gad Perry 204) . The Knight Anole (Anolis equestris) in Florida (Anura:Leptodactylidae) .............................................Brian J. Camposano, Kenneth L. Krysko, Kevin M. Enge, Ellenin M. Donlan, Costa and Michael Granatosky Rica 212 CONSERVATION ALERT . World’s Mammals in Crisis ...............................................................................................................................Raby Nuñez Escalante and Maikol Marin Sánchez .............................. 220 . More Than Mammals .....................................................................................................................................................................
    [Show full text]
  • Systematics of the Fuscus Group of the Frog Genus Leptodactylus (Amphibia, Leptodactylidae)
    SYSTEMATICS OF THE FUSCUS GROUP OF THE FROG GENUS LEPTODACTYLUS (AMPHIBIA, LEPTODACTYLIDAE) By W. RONALD HEYER NATURAL HISTORY MUSEUM OF LOS ANGELES COUNTY SCIENCE BULLETIN 29 • DECEMBER 29, 1978 C<~;, \ TABLE OF CONTENTS ABSTRACT ........................................................................ INTRODUCTION .................................................................... ACKNOWLEDGMENTS AND MUSEUM ABBREVIATIONS ...................................... METHODS AND MATERIALS ........................................................... 2 PoPULATION ANALYSES .............................................................. 6 Leptodactylus albilabris . 6 Leptodactylus labia/is . 9 Leptodactylus fuscus-complex . 10 Leptodactylus bufonius-complex . 22 Leptodactylus latinasus-labialis . 26 Leptodactylus latinasus . 26 SUMMARY OF TAXONOMIC CoNCLUSIONS ......•........................................ 29 NoMENCLATURE . 29 SPECIES AccouNTS ....................... : . 37 Leptodactylus albilabris . 37 Leptodactylus amazonicus-new species . 38 Leptodactylus bufonius . 44 Leptodactylus elenae-new species ............................................... 45 Leptodactylus fragilis . 46 Leptodactylus fuscus . 50 Leptodactylus geminus ............................... ·. 52 Leptodactylus gracilis . 53 Leptodactylus labrosus . 56 Leptodactylus latinasus . 57 Leptodactylus !aurae-new species ............................................... 59 Leptodactylus longirostris ....................................................... 61 Leptodactylus marambaiae . 64
    [Show full text]
  • Crotalus Tancitarensis. the Tancítaro Cross-Banded Mountain Rattlesnake
    Crotalus tancitarensis. The Tancítaro cross-banded mountain rattlesnake is a small species (maximum recorded total length = 434 mm) known only from the upper elevations (3,220–3,225 m) of Cerro Tancítaro, the highest mountain in Michoacán, Mexico, where it inhabits pine-fir forest (Alvarado and Campbell 2004; Alvarado et al. 2007). Cerro Tancítaro lies in the western portion of the Transverse Volcanic Axis, which extends across Mexico from Jalisco to central Veracruz near the 20°N latitude. Its entire range is located within Parque Nacional Pico de Tancítaro (Campbell 2007), an area under threat from manmade fires, logging, avocado culture, and cattle raising. This attractive rattlesnake was described in 2004 by the senior author and Jonathan A. Campbell, and placed in the Crotalus intermedius group of Mexican montane rattlesnakes by Bryson et al. (2011). We calculated its EVS as 19, which is near the upper end of the high vulnerability category (see text for explanation), its IUCN status has been reported as Data Deficient (Campbell 2007), and this species is not listed by SEMARNAT. More information on the natural history and distribution of this species is available, however, which affects its conservation status (especially its IUCN status; Alvarado-Díaz et al. 2007). We consider C. tancitarensis one of the pre-eminent flagship reptile species for the state of Michoacán, and for Mexico in general. Photo by Javier Alvarado-Díaz. Amphib. Reptile Conserv. | http://amphibian-reptile-conservation.org 128 September 2013 | Volume 7 | Number 1 | e71 Copyright: © 2013 Alvarado-Díaz et al. This is an open-access article distributed under the terms of the Creative Commons Attribution–NonCommercial–NoDerivs 3.0 Unported License, which permits unrestricted use for Amphibian & Reptile Conservation 7(1): 128–170.
    [Show full text]
  • Identifying Priority Ecoregions for Amphibian Conservation in the U.S. and Canada
    Acknowledgements This assessment was conducted as part of a priority setting effort for Operation Frog Pond, a project of Tree Walkers International. Operation Frog Pond is designed to encourage private individuals and community groups to become involved in amphibian conservation around their homes and communities. Funding for this assessment was provided by The Lawrence Foundation, Northwest Frog Fest, and members of Tree Walkers International. This assessment would not be possible without data provided by The Global Amphibian Assessment, NatureServe, and the International Conservation Union. We are indebted to their foresight in compiling basic scientific information about species’ distributions, ecology, and conservation status; and making these data available to the public, so that we can provide informed stewardship for our natural resources. I would also like to extend a special thank you to Aaron Bloch for compiling conservation status data for amphibians in the United States and to Joe Milmoe and the U.S. Fish and Wildlife Service, Partners for Fish and Wildlife Program for supporting Operation Frog Pond. Photo Credits Photographs are credited to each photographer on the pages where they appear. All rights are reserved by individual photographers. All photos on the front and back cover are copyright Tim Paine. Suggested Citation Brock, B.L. 2007. Identifying priority ecoregions for amphibian conservation in the U.S. and Canada. Tree Walkers International Special Report. Tree Walkers International, USA. Text © 2007 by Brent L. Brock and Tree Walkers International Tree Walkers International, 3025 Woodchuck Road, Bozeman, MT 59715-1702 Layout and design: Elizabeth K. Brock Photographs: as noted, all rights reserved by individual photographers.
    [Show full text]
  • Antipredator Mechanisms of Leptodactylus Syphax Bokermann, 1969 (Anura: Leptodactylidae)
    Herpetology Notes, volume 14: 257-261 (2021) (published online on 01 February 2021) Antipredator mechanisms of Leptodactylus syphax Bokermann, 1969 (Anura: Leptodactylidae) Felipe P. Sena1, Rayone A. Silva1, Antonia Joyce S. Santos1, Claylton A. Costa1,2, Sâmia Caroline M. Araújo1,3, and Etielle B. Andrade1,* Amphibians are important components of the Sá et al., 2014; Frost, 2021). food chain acting as prey for both vertebrates and Leptodactylus syphax Bokermann, 1969 is a medium- invertebrates (Toledo, 2005; Toledo et al., 2007). This sized species, widely distributed in the central and prey-predator relationship leads species make use of northeastern of Brazil, southern Paraguay, and eastern defensive strategies to deter, avoid or confuse predators, Bolivia (Frost, 2021). It was initially included in the L. using morphological, physiological, and behavioural pentadactylus group by Heyer (1969), and posteriorly responses selected by natural selection (Duellman and was placed in the L. fuscus group based on molecular and Trueb, 1994; Wells, 2007). Anurans developed several bioacoustic characters (de Sá et al., 2014). Individuals anti-predatory mechanisms, placed in three phases of this species have smooth skin with tubers on the back (avoid detection, prevent attacks, and counterattack), limited by the sacral and post-sacral regions, and males overall involving aposematic colouration, defensive develop spines on the hands and chest and hypertrophied posture, and toxin production (Toledo and Jared, 1995; arms to hold the females during the reproductive period Toledo and Haddad, 2009; Toledo et al., 2011; Ferreira (Heyer et al., 2010; de Sá et al., 2014). et al., 2019). Despite increasing in recent years, studies on the Leptodactylidae currently comprises 231 species anurans defensive behaviour are still scarce (Toledo et of large, medium, and small-sized frogs distributed al., 2011).
    [Show full text]
  • Bibliography of the Anurans of the United States and Canada. Version 2, Updated and Covering the Period 1709 – 2012
    January 2018 Open Access Publishing Volume 13, Monograph 7 A female Western Toad (Anaxyrus boreas) from Garibaldi Provincial Park, British Columbia, Canada. This large bufonid occurs throughout much of Western North America. The IUCN lists it as Near Threatened because it is probably in significant decline (> 30% over 10 years) due to disease.(Photographed by C. Kenneth Dodd). Bibliography of the Anurans of the United States and Canada. Version 2, Updated and Covering the Period 1709 – 2012. Monograph 7. C. Kenneth Dodd, Jr. ISSN: 1931-7603 Indexed by: Zoological Record, Scopus, Current Contents / Agriculture, Biology & Environmental Sciences, Journal Citation Reports, Science Citation Index Extended, EMBiology, Biology Browser, Wildlife Review Abstracts, Google Scholar, and is in the Directory of Open Access Journals. BIBLIOGRAPHY OF THE ANURANS OF THE UNITED STATES AND CANADA. VERSION 2, UPDATED AND COVERING THE PERIOD 1709 – 2012. MONOGRAPH 7. C. KENNETH DODD, JR. Department of Wildlife Ecology and Conservation, University of Florida, Gainesville, Florida, USA 32611. Copyright © 2018. C. Kenneth Dodd, Jr. All Rights Reserved. Please cite this monograph as follows: Dodd, C. Kenneth, Jr. 2018. Bibliography of the anurans of the United States and Canada. Version 2, Updated and Covering the Period 1709 - 2012. Herpetological Conservation and Biology 13(Monograph 7):1-328. Table of Contents TABLE OF CONTENTS i PREFACE ii ABSTRACT 1 COMPOSITE BIBLIOGRAPHIC TRIVIA 1 LITERATURE CITED 2 BIBLIOGRAPHY 2 FOOTNOTES 325 IDENTICAL TEXTS 325 CATALOGUE OF NORTH AMERICAN AMPHIBIANS AND REPTILES 326 ADDITIONAL ANURAN-INCLUSIVE BIBLIOGRAPHIES 326 AUTHOR BIOGRAPHY 328 i Preface to Version 2: An Expanded and Detailed Resource. MALCOLM L.
    [Show full text]
  • Study of Amphibians of the Parque Natural
    Envr 451- Research in Panama April 25th, 2008 Amphibians of the Parque Natural Metropolitano, Panama A study of amphibians and the development of an environmental education program Guillaume Majeau-Bettez Adèle Michon Louis-Philippe Potvin Victor Thomasson Presented to Dr Roberto Ibañez McGill University Under the Supervision of Rafael Gómez and Amelia Muñoz Parque Natural Metropolitano 2 Executive Summary : Study of Amphibians of the Parque Natural Metropolitano By Guillaume Majeau-Bettez, Adèle Michon, Louis-Philippe Potvin, Victor Thomasson Parque Natural Metropolitano, Ave. Juan Pablo II, Apartado 5499, Balboa, Ancón, Panamá, República de Panamá. The Parque Natural Metropolitano (PNM) is definitely unique in many aspects. First of all, it is one of the only parks in the world that is found in the limits of a city. The Parque Natural Metropolitano is part of the Canal Zone protection corridor, along other major parks: Camino de Cruces and Soberania National Park. Due to the increasing pressure on land, it also represents one of the last refuges for dwellers of the Central-American dry tropical forest. Worldwide, the population of frogs is decreasing at an alarming rate. There is certainly fear to be felt from this change, since these creatures are considered to be indicators for environmental health. Because of their unique life traits, amphibians hold an extremely important ecological importance. They have been present on Earth for 360 millions of years, survived numerous mass extinctions periods, and so their decline should be taken very seriously. The objective of the project was to evaluate the diversity and the general state of the amphibians found in the park.
    [Show full text]
  • Anfibios Y Reptiles De Los Bosques De La Aguadita, Región Del Salto De Tequendama Y Puerto Salgar Departamento De Cundinamarca
    Anfibios y reptiles de los bosques de La Aguadita, región del Salto de Tequendama y Puerto Salgar departamento de Cundinamarca Informe final por José Vicente Rueda Almonacid Conservación Internacional Colombia Convenio # 00597 Agosto 19 de 2009 Tecnología análisis de la situación actual de las actividades de ecoturismo en la Reserva Forestal Pro- tectora Bosque Oriental de Bogotá. Recomendaciones para su reglamentación y manejo EDGAR ALFONSO BEJARANO MÉNDEZ DIRECTOR GENERAL Corporación Autónoma Regional de Cundinamarca - CAR FABIO ARJONA DIRECTOR EJECUTIVO Conservación Internacional-Colombia JOSÉ VICENTE RODRÍGUEZ MAHECHA DIRECTOR CIENTÍFICO Conservación Internacional-Colombia HEBERT GONZALO RIVERA SUBDIRECTOR DE ADMINISTRACIÓN DE RECURSOS NATURALES Y ÁREAS PROTEGIDAS Corporación Autónoma Regional de Cundinamarca - CAR DALILA CAMELO SALAMANCA Bióloga - Subdirección de Administración de Recursos Naturales y Áreas Protegidas Corporación Autónoma Regional de Cundinamarca – CAR. DIRECTOR DEL PROYECTO JOSÉ VICENTE RUEDA-ALMONACID Fotografías: JOSÉ VICENTE RUEDA-ALMONACID & GIOVANNI CHAVEZ, salvo que se indique el autor. Diagramación & Diseño ANDRÉS GONZÁLEZ HERNÁNDEZ MAYO 2010 BOGOTÁ D.C. Página opuesta pared de roca en el Parque Natural Chicaque 2 3 • Anfibios y reptiles de los Bosques de La Aguadita, Región Salto del Tequendama y Puerto Salgar - Departamento de Cundinamarca Tabla de Contenido Introducción ..............................................................................................................6 Metodología ..............................................................................................................8
    [Show full text]