Eastern Dwarf Treefrog (Litoria Fallax) 1 Native Range and Status in the United States
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Return Rates of Male Hylid Frogs Litoria Genimaculata, L. Nannotis, L
Vol. 11: 183–188, 2010 ENDANGERED SPECIES RESEARCH Published online April 16 doi: 10.3354/esr00253 Endang Species Res OPENPEN ACCESSCCESS Return rates of male hylid frogs Litoria genimaculata, L. nannotis, L. rheocola and Nyctimystes dayi after toe-tipping Andrea D. Phillott1, 2,*, Keith R. McDonald1, 3, Lee F. Skerratt1, 2 1Amphibian Disease Ecology Group and 2School of Public Health, Tropical Medicine and Rehabilitation Sciences, James Cook University, Townsville, Queensland 4811, Australia 3Threatened Species Branch, Department of Environment and Resource Management, PO Box 975, Atherton, Queensland 4883, Australia ABSTRACT: Toe-tipping is a commonly used procedure for mark-recapture studies of frogs, although it has been criticised for its potential influence on frog behaviour, site fidelity and mortality. We com- pared 24 h return rates of newly toe-tipped frogs to those previously toe-tipped and found no evi- dence of a stress response reflected by avoidance behaviour for 3 species: Litoria genimaculata, L. rheocola and Nyctimystes dayi. L. nannotis was the only studied species to demonstrate a greater reaction to toe-tipping than handling alone; however, return rates (65%) in the 1 to 3 mo after mark- ing were the highest of any species, showing that the reaction did not endure. The comparatively milder short-term response to toe-tipping in N. dayi (24% return rate) may have been caused by the species’ reduced opportunity for breeding. Intermediate-term return rates were relatively high for 2 species, L. nannotis and L. genimaculata, given their natural history, suggesting there were no major adverse effects of toe-tipping. Longer-term adverse effects could not be ruled out for L. -
Catalogue of the Amphibians of Venezuela: Illustrated and Annotated Species List, Distribution, and Conservation 1,2César L
Mannophryne vulcano, Male carrying tadpoles. El Ávila (Parque Nacional Guairarepano), Distrito Federal. Photo: Jose Vieira. We want to dedicate this work to some outstanding individuals who encouraged us, directly or indirectly, and are no longer with us. They were colleagues and close friends, and their friendship will remain for years to come. César Molina Rodríguez (1960–2015) Erik Arrieta Márquez (1978–2008) Jose Ayarzagüena Sanz (1952–2011) Saúl Gutiérrez Eljuri (1960–2012) Juan Rivero (1923–2014) Luis Scott (1948–2011) Marco Natera Mumaw (1972–2010) Official journal website: Amphibian & Reptile Conservation amphibian-reptile-conservation.org 13(1) [Special Section]: 1–198 (e180). Catalogue of the amphibians of Venezuela: Illustrated and annotated species list, distribution, and conservation 1,2César L. Barrio-Amorós, 3,4Fernando J. M. Rojas-Runjaic, and 5J. Celsa Señaris 1Fundación AndígenA, Apartado Postal 210, Mérida, VENEZUELA 2Current address: Doc Frog Expeditions, Uvita de Osa, COSTA RICA 3Fundación La Salle de Ciencias Naturales, Museo de Historia Natural La Salle, Apartado Postal 1930, Caracas 1010-A, VENEZUELA 4Current address: Pontifícia Universidade Católica do Río Grande do Sul (PUCRS), Laboratório de Sistemática de Vertebrados, Av. Ipiranga 6681, Porto Alegre, RS 90619–900, BRAZIL 5Instituto Venezolano de Investigaciones Científicas, Altos de Pipe, apartado 20632, Caracas 1020, VENEZUELA Abstract.—Presented is an annotated checklist of the amphibians of Venezuela, current as of December 2018. The last comprehensive list (Barrio-Amorós 2009c) included a total of 333 species, while the current catalogue lists 387 species (370 anurans, 10 caecilians, and seven salamanders), including 28 species not yet described or properly identified. Fifty species and four genera are added to the previous list, 25 species are deleted, and 47 experienced nomenclatural changes. -
The Journey of Life of the Tiger-Striped Leaf Frog Callimedusa Tomopterna (Cope, 1868): Notes of Sexual Behaviour, Nesting and Reproduction in the Brazilian Amazon
Herpetology Notes, volume 11: 531-538 (2018) (published online on 25 July 2018) The journey of life of the Tiger-striped Leaf Frog Callimedusa tomopterna (Cope, 1868): Notes of sexual behaviour, nesting and reproduction in the Brazilian Amazon Thainá Najar1,2 and Lucas Ferrante2,3,* The Tiger-striped Leaf Frog Callimedusa tomopterna 2000; Venâncio & Melo-Sampaio, 2010; Downie et al, belongs to the family Phyllomedusidae, which is 2013; Dias et al. 2017). constituted by 63 described species distributed in In 1975, Lescure described the nests and development eight genera, Agalychnis, Callimedusa, Cruziohyla, of tadpoles to C. tomopterna, based only on spawns that Hylomantis, Phasmahyla, Phrynomedusa, he had found around the permanent ponds in the French Phyllomedusa, and Pithecopus (Duellman, 2016; Guiana. However, the author mentions a variation in the Frost, 2017). The reproductive aspects reported for the number of eggs for some spawns and the use of more than species of this family are marked by the uniqueness of one leaf for confection in some nests (Lescure, 1975). egg deposition, placed on green leaves hanging under The nests described by Lescure in 1975 are probably standing water, where the tadpoles will complete their from Phyllomedusa vailantii as reported by Lescure et development (Haddad & Sazima, 1992; Pombal & al. (1995). The number of eggs in the spawns reported Haddad, 1992; Haddad & Prado, 2005). However, by Lescure (1975) diverge from that described by other exist exceptions, some species in the genus Cruziohyla, authors such as Neckel-Oliveira & Wachlevski, (2004) Phasmahylas and Prhynomedusa, besides the species and Lima et al. (2012). In addition, the use of more than of the genus Agalychnis and Pithecopus of clade one leaf for confection in the nest mentioned by Lescure megacephalus that lay their eggs in lotic environments (1975), are characteristic of other species belonging to (Haddad & Prado, 2005; Faivovich et al. -
The Phylogenetic Relationships of the Charismatic Poster Frogs, Phyllomedusinae (Anura, Hylidae)
Cladistics Cladistics 26 (2010) 227–261 10.1111/j.1096-0031.2009.00287.x The phylogenetic relationships of the charismatic poster frogs, Phyllomedusinae (Anura, Hylidae) Julia´ n Faivovicha,*, Ce´ lio F. B. Haddadb,De´ lio Baeˆ tac, Karl-Heinz Jungferd, Guilherme F. R. A´ lvarese, Reuber A. Branda˜ oe, Christopher Sheilf, Lucas S. Barrientosg,Ce´ sar L. Barrio-Amoro´ sh, Carlos A. G. Cruzc and Ward C. Wheeleri aDivisio´n Herpetologı´a, Museo Argentino de Ciencias Naturales-CONICET, Angel Gallardo 470, C1405DJR, Buenos Aires, Argentina; Departamento de Zoologia, I.B., Universidade Estadual Paulista, Rio Claro, CEP 13506-900, Sa˜o Paulo, Brazil; and Herpetology, Division of Vertebrate Zoology, American Museum of Natural History, New York, USA; bDepartamento de Zoologia, I.B., Universidade Estadual Paulista, Rio Claro, CEP 13506-900, Sa˜o Paulo, Brazil; cSetor de Herpetologia, Departamento de Vertebrados, Museu Nacional, Universidade Federal do Rio de Janeiro, Quinta da Boa Vista, s ⁄ n°,Sa˜o Cristo´va˜o, CEP 20940-040, Rio de Janeiro, RJ, Brazil; dPanoramastr. 14, 74405 Gaildorf, Germany; eLaborato´rio de Fauna e Unidades de Conservac¸a˜o, Departamento de Engenharia Florestal, Universidade de Brası´lia, Brası´lia-DF, CEP 70910-900, Brazil; fDepartment of Biology, Dolan Center for Science & Technology, John Carroll University, 20700 North Park Boulevard, University Heights, OH 44118, USA; gInstituto de Ciencias Naturales, Universidad Nacional de Colombia, calle 53, 2° edificio Bogota´, Colombia; hFundacio´n Andı´genA, Apartado Postal 210, 5101-A Me´rida, Venezuela; iDivision of Invertebrate Zoology, American Museum of Natural History, Central Park West at 79th St, New York, NY 10024, USA Accepted 8 August 2009 Abstract The leaf or monkey frogs of the hylid subfamily Phyllomedusinae are a unique group of charismatic anurans. -
Southern Brown Tree Frog
Our Wildlife Fact Sheet Southern Brown Tree Frog Southern Brown Tree Frogs are one of Victoria’s common frog species. Scientific name Litoria ewingi Did you know? The Southern Brown Tree Frog is an agile hunter. It can leap to catch insects in mid flight. Their large sticky toes make them great climbers. Figure 1. Southern Brown Tree Frog metamorphs © A. Houston Female Southern Brown Tree Frogs can lay up to 600 DSE 2008 eggs at a time. Distribution It takes between 12 and 26 weeks for Southern Brown Southern Brown Tree Frogs occur in southern Victoria, tadpoles to turn into frogs. Tasmania and along the south coast of New South Wales. Description They are found across most of southern, central and Southern Brown Tree Frogs grow up to about 50 mm in north-eastern Victoria, but do not occur in the north- length. west corner of the state. In north-central Victoria and in Their colour is true to their name as they are brown on parts of the state’s north-east they are replaced by the their backs. The backs of their thighs are yellowish to closely-related Plains Brown Tree Frog (Litoria bright orange, and they have a white grainy belly. They paraewingi). also have a distinctive white stripe from the eye to their fore-leg. Their skin is smooth with small lumps. They have webbing on their feet that goes half way up their toes while their fingers have no webbing at all. Breeding males have a light brown vocal sac. Diet Southern Brown Tree Frogs feed mainly on flying insects such as mosquitoes, moths and flies. -
Conservation Advice Litoria Dayi Lace-Eyed Tree Frog
THREATENED SPECIES SCIENTIFIC COMMITTEE Established under the Environment Protection and Biodiversity Conservation Act 1999 The Minister’s delegate approved this Conservation Advice on 13/07/2017. Conservation Advice Litoria dayi lace-eyed tree frog Conservation Status Litoria dayi (lace-eyed tree frog) is listed as Endangered under the Environment Protection and Biodiversity Conservation Act 1999 (Cwlth) (EPBC Act) effective 16 July 2000. The species is eligible for listing under the EPBC Act as on 16 July 2000 it was listed as Endangered under Schedule 1 of the preceding Act, the Endangered Species Protection Act 1992 (Cwlth). Species can also be listed as threatened under state and territory legislation. For information on the current listing status of this species under relevant state or territory legislation, see http://www.environment.gov.au/cgi-bin/sprat/public/sprat.pl . The main factor that was the cause of the species being eligible for listing in the Endangered category was a dramatic range contraction with an observed reduction in population size of greater than 50 percent. Populations are no longer present at altitudes greater than 300 m, likely due to chytridiomycosis (Hero et al. 2004). This species’ status under the EBPC Act is currently being reviewed as part of a species expert assessment plan for frogs. Description The lace-eyed tree frog was recently transferred to the genus Litoria from the genus Nyctimystes after Kraus (2013) showed that it did not meet the morphological characteristics for assignment to that genus (Cogger 2014). This species is a small to medium sized frog growing to 50 mm in snout-to-vent length. -
An Overdue Review and Reclassification of the Australasian
AustralasianAustralasian JournalJournal ofof HerpetologyHerpetology ISSN 1836-5698 (Print) ISSN 1836-5779 (Online) Hoser, R. T. 2020. For the first time ever! An overdue review and reclassification of Australasian Tree Frogs (Amphibia: Anura: Pelodryadidae), including formal descriptions of 12 tribes, 11 subtribes, 34 genera, 26 subgenera, 62 species and 12 subspecies new to science. Australasian Journal of Herpetology 44-46:1-192. ISSUE 46, PUBLISHED 5 JUNE 2020 Hoser, R. T. 2020. For the first time ever! An overdue review and reclassification of Australasian Tree Frogs (Amphibia: Anura: Pelodryadidae), including formal descriptions of 12 tribes, 11 subtribes, 34 genera, 26 130 Australasiansubgenera, 62 species Journal and 12 subspecies of Herpetologynew to science. Australasian Journal of Herpetology 44-46:1-192. ... Continued from AJH Issue 45 ... zone of apparently unsuitable habitat of significant geological antiquity and are therefore reproductively Underside of thighs have irregular darker patches and isolated and therefore evolving in separate directions. hind isde of thigh has irregular fine creamish coloured They are also morphologically divergent, warranting stripes. Skin is leathery and with numerous scattered identification of the unnamed population at least to tubercles which may or not be arranged in well-defined subspecies level as done herein. longitudinal rows, including sometimes some of medium to large size and a prominent one on the eyelid. Belly is The zone dividing known populations of each species is smooth except for some granular skin on the lower belly only about 30 km in a straight line. and thighs. Vomerine teeth present, but weakly P. longirostris tozerensis subsp. nov. is separated from P. -
A Preliminary Risk Assessment of Cane Toads in Kakadu National Park Scientist Report 164, Supervising Scientist, Darwin NT
supervising scientist 164 report A preliminary risk assessment of cane toads in Kakadu National Park RA van Dam, DJ Walden & GW Begg supervising scientist national centre for tropical wetland research This report has been prepared by staff of the Environmental Research Institute of the Supervising Scientist (eriss) as part of our commitment to the National Centre for Tropical Wetland Research Rick A van Dam Environmental Research Institute of the Supervising Scientist, Locked Bag 2, Jabiru NT 0886, Australia (Present address: Sinclair Knight Merz, 100 Christie St, St Leonards NSW 2065, Australia) David J Walden Environmental Research Institute of the Supervising Scientist, GPO Box 461, Darwin NT 0801, Australia George W Begg Environmental Research Institute of the Supervising Scientist, GPO Box 461, Darwin NT 0801, Australia This report should be cited as follows: van Dam RA, Walden DJ & Begg GW 2002 A preliminary risk assessment of cane toads in Kakadu National Park Scientist Report 164, Supervising Scientist, Darwin NT The Supervising Scientist is part of Environment Australia, the environmental program of the Commonwealth Department of Environment and Heritage © Commonwealth of Australia 2002 Supervising Scientist Environment Australia GPO Box 461, Darwin NT 0801 Australia ISSN 1325-1554 ISBN 0 642 24370 0 This work is copyright Apart from any use as permitted under the Copyright Act 1968, no part may be reproduced by any process without prior written permission from the Supervising Scientist Requests and inquiries concerning reproduction -
Antipredator Mechanisms of Post-Metamorphic Anurans: a Global Database and Classification System
Utah State University DigitalCommons@USU Ecology Center Publications Ecology Center 5-1-2019 Antipredator Mechanisms of Post-Metamorphic Anurans: A Global Database and Classification System Rodrigo B. Ferreira Utah State University Ricardo Lourenço-de-Moraes Universidade Estadual de Maringá Cássio Zocca Universidade Vila Velha Charles Duca Universidade Vila Velha Karen H. Beard Utah State University Edmund D. Brodie Jr. Utah State University Follow this and additional works at: https://digitalcommons.usu.edu/eco_pubs Part of the Ecology and Evolutionary Biology Commons Recommended Citation Ferreira, R.B., Lourenço-de-Moraes, R., Zocca, C. et al. Behav Ecol Sociobiol (2019) 73: 69. https://doi.org/ 10.1007/s00265-019-2680-1 This Article is brought to you for free and open access by the Ecology Center at DigitalCommons@USU. It has been accepted for inclusion in Ecology Center Publications by an authorized administrator of DigitalCommons@USU. For more information, please contact [email protected]. 1 Antipredator mechanisms of post-metamorphic anurans: a global database and 2 classification system 3 4 Rodrigo B. Ferreira1,2*, Ricardo Lourenço-de-Moraes3, Cássio Zocca1, Charles Duca1, Karen H. 5 Beard2, Edmund D. Brodie Jr.4 6 7 1 Programa de Pós-Graduação em Ecologia de Ecossistemas, Universidade Vila Velha, Vila Velha, ES, 8 Brazil 9 2 Department of Wildland Resources and the Ecology Center, Utah State University, Logan, UT, United 10 States of America 11 3 Programa de Pós-Graduação em Ecologia de Ambientes Aquáticos Continentais, Universidade Estadual 12 de Maringá, Maringá, PR, Brazil 13 4 Department of Biology and the Ecology Center, Utah State University, Logan, UT, United States of 14 America 15 16 *Corresponding author: Rodrigo B. -
ARAZPA YOTF Infopack.Pdf
ARAZPA 2008 Year of the Frog Campaign Information pack ARAZPA 2008 Year of the Frog Campaign Printing: The ARAZPA 2008 Year of the Frog Campaign pack was generously supported by Madman Printing Phone: +61 3 9244 0100 Email: [email protected] Front cover design: Patrick Crawley, www.creepycrawleycartoons.com Mobile: 0401 316 827 Email: [email protected] Front cover photo: Pseudophryne pengilleyi, Northern Corroboree Frog. Photo courtesy of Lydia Fucsko. Printed on 100% recycled stock 2 ARAZPA 2008 Year of the Frog Campaign Contents Foreword.........................................................................................................................................5 Foreword part II ………………………………………………………………………………………… ...6 Introduction.....................................................................................................................................9 Section 1: Why A Campaign?....................................................................................................11 The Connection Between Man and Nature........................................................................11 Man’s Effect on Nature ......................................................................................................11 Frogs Matter ......................................................................................................................11 The Problem ......................................................................................................................12 The Reason -
3Systematics and Diversity of Extant Amphibians
Systematics and Diversity of 3 Extant Amphibians he three extant lissamphibian lineages (hereafter amples of classic systematics papers. We present widely referred to by the more common term amphibians) used common names of groups in addition to scientifi c Tare descendants of a common ancestor that lived names, noting also that herpetologists colloquially refer during (or soon after) the Late Carboniferous. Since the to most clades by their scientifi c name (e.g., ranids, am- three lineages diverged, each has evolved unique fea- bystomatids, typhlonectids). tures that defi ne the group; however, salamanders, frogs, A total of 7,303 species of amphibians are recognized and caecelians also share many traits that are evidence and new species—primarily tropical frogs and salaman- of their common ancestry. Two of the most defi nitive of ders—continue to be described. Frogs are far more di- these traits are: verse than salamanders and caecelians combined; more than 6,400 (~88%) of extant amphibian species are frogs, 1. Nearly all amphibians have complex life histories. almost 25% of which have been described in the past Most species undergo metamorphosis from an 15 years. Salamanders comprise more than 660 species, aquatic larva to a terrestrial adult, and even spe- and there are 200 species of caecilians. Amphibian diver- cies that lay terrestrial eggs require moist nest sity is not evenly distributed within families. For example, sites to prevent desiccation. Thus, regardless of more than 65% of extant salamanders are in the family the habitat of the adult, all species of amphibians Plethodontidae, and more than 50% of all frogs are in just are fundamentally tied to water. -
Wiens Et Al. Page: 1
Wiens et al. page: 1 1 Supporting Information 2 Appendix S1 3 Expanded Materials and Methods 4 Appendix S1.A. Local Sites. We obtained data on the local species composition 5 of 123 sites throughout the range of Hylidae (Tables S1–S3). Our major source of 6 data was published studies of the amphibian faunas of local sites. We focused on 7 well-studied site, typically of several km2 in size, that represent a single biome or 8 habitat (e.g. tropical lowland rainforest), but include multiple microhabitats (e.g. 9 forest, stream edge, pond). We generally excluded sites spanning multiple 10 biomes, and from poorly known regions in which the observed hylid richness 11 was much lower than for other sites in the same region (possibly reflecting poor 12 sampling or human impacts). In some cases, we also included species lists from 13 national parks or reserves, particularly for regions where we could corroborate 14 these lists with published range maps (e.g. U.S., Australia). For some areas 15 having few obvious sites, we picked localities where large numbers of hylid 16 species have been collected, based on literature or museum records. For areas 17 with very low hylid diversity (e.g., Europe, Asia, Western North America), we 18 used museum records. 19 For most analyses, we used a single, well-studied locality to represent 20 each major biogeographic region (Table 1), in order to reduce potential problems 21 of uneven numbers of sites among biogeographic regions, spatial 22 autocorrelation, and inadequately surveyed sites. For a given region, we used Wiens et al.