Sanches PR, Et Al. First Record of Polymelia in the Paradox Frog Pseudis Paradoxa (Linnaeus, Copyright© Sanches PR, Et Al
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Histomorfología De La Glándula Tiroides Durante La Ontogenia En Pseudis Paradoxa (Anura, Hylidae)
Tesis Doctoral Histomorfología de la glándula tiroides durante la ontogenia en Pseudis paradoxa (Anura, Hylidae) Cruz, Julio César 2017 Este documento forma parte de las colecciones digitales de la Biblioteca Central Dr. Luis Federico Leloir, disponible en bibliotecadigital.exactas.uba.ar. Su utilización debe ser acompañada por la cita bibliográfica con reconocimiento de la fuente. This document is part of the digital collection of the Central Library Dr. Luis Federico Leloir, available in bibliotecadigital.exactas.uba.ar. It should be used accompanied by the corresponding citation acknowledging the source. Cita tipo APA: Cruz, Julio César. (2017). Histomorfología de la glándula tiroides durante la ontogenia en Pseudis paradoxa (Anura, Hylidae). Facultad de Ciencias Exactas y Naturales. Universidad de Buenos Aires. https://hdl.handle.net/20.500.12110/tesis_n6259_Cruz Cita tipo Chicago: Cruz, Julio César. "Histomorfología de la glándula tiroides durante la ontogenia en Pseudis paradoxa (Anura, Hylidae)". Facultad de Ciencias Exactas y Naturales. Universidad de Buenos Aires. 2017. https://hdl.handle.net/20.500.12110/tesis_n6259_Cruz Dirección: Biblioteca Central Dr. Luis F. Leloir, Facultad de Ciencias Exactas y Naturales, Universidad de Buenos Aires. Contacto: bibliotecadigital.exactas.uba.ar Intendente Güiraldes 2160 - C1428EGA - Tel. (++54 +11) 4789-9293 UNIVERSIDAD DE BUENOS AIRES Facultad de Ciencias Exactas y Naturales Departamento de Biodiversidad y Biología Experimental Histomorfología de la glándula tiroides durante la ontogenia -
Notes on the Paradox Frog, Pseudis Paradoxa, in Bolivia
British Herpetological Society Bullton. No. 68. 1999 NOTES ON THE PARADOX FROG, PSEUDIS PARADOXA, IN BOLIVIA IGNACIO DE LA RIVA Department of Biodiversity and Evolutionary Biology Museo Nacional de Ciencias Naturales a Jose Gutierrez Abascal 2, 28006 Madrid, Spain INTRODUCTION The South American Paradox Frog, Pseudis paradoxa (Plate. 1) is primarily a dweller of open, lowland areas, where it inhabits marshes, ponds and other types of lentic water bodies. It has a discontinuous distribution from Colombia to Argentina. Inter- populational differences primarily in colour pattern, as well a in some other features, have led to the recognition of seven subspecies [P. p. bolbodactyla and P. p. fusca were recently proposed to be elevated to specific status (Caramaschi and Cruz, 1998)]. DISTRIBUTION AND SUBSPECIES IN BOLIVIA For taxonomic and biogeographical reasons, the lowlands of Bolivia are an interesting area with respect to this frog. The distribution of the species in this country is poorly known. The first Bolivian record of P. paradoxa was provided by Muller and Hellmich (1936) at San Fermiin, Department of Santa Cruz. Since then, it was reported at some other localities, mostly in the Department of Santa Cruz [see De la Riva (1990) and below]. It was interesting that it was also discovered at two localities in southeastern Peru (Duellman and Salas, 1991; Henle, 1992). These discoveries made plausible that it ranges throughout the intermediate area of extensive, suitable habitat of humid savannas in the Bolivian Department of Beni. However, there is a surprising scarcity of published records for this huge and relatively (by Bolivian standards) well surveyed zone. -
Ecological Functions of Neotropical Amphibians and Reptiles: a Review
Univ. Sci. 2015, Vol. 20 (2): 229-245 doi: 10.11144/Javeriana.SC20-2.efna Freely available on line REVIEW ARTICLE Ecological functions of neotropical amphibians and reptiles: a review Cortés-Gomez AM1, Ruiz-Agudelo CA2 , Valencia-Aguilar A3, Ladle RJ4 Abstract Amphibians and reptiles (herps) are the most abundant and diverse vertebrate taxa in tropical ecosystems. Nevertheless, little is known about their role in maintaining and regulating ecosystem functions and, by extension, their potential value for supporting ecosystem services. Here, we review research on the ecological functions of Neotropical herps, in different sources (the bibliographic databases, book chapters, etc.). A total of 167 Neotropical herpetology studies published over the last four decades (1970 to 2014) were reviewed, providing information on more than 100 species that contribute to at least five categories of ecological functions: i) nutrient cycling; ii) bioturbation; iii) pollination; iv) seed dispersal, and; v) energy flow through ecosystems. We emphasize the need to expand the knowledge about ecological functions in Neotropical ecosystems and the mechanisms behind these, through the study of functional traits and analysis of ecological processes. Many of these functions provide key ecosystem services, such as biological pest control, seed dispersal and water quality. By knowing and understanding the functions that perform the herps in ecosystems, management plans for cultural landscapes, restoration or recovery projects of landscapes that involve aquatic and terrestrial systems, development of comprehensive plans and detailed conservation of species and ecosystems may be structured in a more appropriate way. Besides information gaps identified in this review, this contribution explores these issues in terms of better understanding of key questions in the study of ecosystem services and biodiversity and, also, of how these services are generated. -
Pseudis Paradoxa
__all_short_notes_sHoRt_note.qxd 12.02.2016 10:37 seite 26 192 sHoRt note HeRPetoZoa 28 (3/4) Wien, 30. Jänner 2016 sHoRt note Pseudis paradoxa (Linnaeus , 1758 ): um body size (svL 45-75 mm), relatively northward extension of the known small head and protruding eyes in dorsolat - distribution range in Colombia eral position with a yellow iris crossed by a brown bar ( LesCuRe & M aRty 2000). its common name makes reference to the extra - in spite of increasing knowledge about ordinary size of the tadpole relative to that the diversity of anuran amphibians in Co - of adult individuals ( eMeRson 1988). the lombia ( BeRnaL & L ynCH 2008; GaLvis - distribution of this species covers Colom - PeñueLa et al. 2011; aCosta -G aLvis 2012), bia, Guyana, suriname, Brazil, Bolivia, there are still many gaps with regard to the Peru, venezuela and the islands of trinidad known distribution of the species. Detec- and tobago ( FRost 2014). in Colombia, it tion of the presence of anuran species in is present in the the lower Rio Magdalena places from which they were previously area (Departments of antioquia, atlántico, unrecorded establishes a baseline for the Bolivar, Cesar, Cordoba, Magdalena, study of species richness, optimizing con - santander, sucre) as well as the departments servation plans, and research in the fields of of arauca and Meta in the eastern region of taxonomy, systematics and natural history. Colombia (Fig. 1a) ( RenGiFo & L unDBeRG this is the first report on the occurrence of 1999; aCosta -G aLvis 2000; Cuentas - the hylid frog Pseudis paradoxa (Linnaeus , MontaLvo 2002; aCosta -G aLvis 2014). 1758 ) in the north Colombian department of the authors recorded several individu - Guajira (Fig. -
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. -
Predation on the Paradoxical Frog Pseudis Paradoxa (Anura, Hylidae, Pseudinae) by the Great Egret Ardea Alba (Aves, Pelecaniformes, Ardeidae)
Herpetology Notes, volume 13: 965-967 (2020) (published online on 26 November 2020) Predation on the paradoxical frog Pseudis paradoxa (Anura, Hylidae, Pseudinae) by the great egret Ardea alba (Aves, Pelecaniformes, Ardeidae) Aline Emanuele Oliveira-Souza1,*, Girlan Dias-Silva2, and Carlos Eduardo Costa-Campos1 Anurans represent an important food source for a Fieldwork was conducted at the Ecological Station of wide range of invertebrates (Toledo, 2005; Toledo Maracá-Jipioca (ESEC), located in the coast of Amapá et al., 2007) and vertebrates, including birds (Poulin State, eastern Amazon, Brazil. The ESEC comprises et al., 2001; Toledo et al., 2004; Lopes et al., 2005). the Maracá and Jipioca islands; Maracá is divided Because they tend to occur in association with aquatic into North and South islands, which are separated by a environments, anurans are more vulnerable to aquatic channel called Igarapé do Inferno. The terrain is flat and predators (Toledo, 2003). In a review of records of composed by floodplains, mangroves, bamboo forest and vertebrate predators of anurans, Aves was the third most small areas of terra firme forest (França et al., 2018). On representative group, comprising approximately 20% of 11 October 2017 at 07:56 h, a camera-trapping, installed published reports (Toledo et al., 2007). Herein we report for the monitoring of jaguars, recorded an individual of on a predation event on an individual of the paradoxical A. alba preying upon an individual of P. paradoxa on frog Pseudis paradoxa (Linnaeus, 1758) by the great the margin of a pond in Bibi Lake (GPS coordinates egret Ardea alba (Linnaeus, 1758), in a coastal island = 2.1448°N; 50.5248°W), located at Maracá North of northern Brazil. -
What the Largest Tadpole Feeds On? a Detailed Analysis of the Diet Composition of Pseudis Minuta Tadpoles (Hylidae, Dendropsophini)
Anais da Academia Brasileira de Ciências (2016) 88(3): 1397-1400 (Annals of the Brazilian Academy of Sciences) Printed version ISSN 0001-3765 / Online version ISSN 1678-2690 http://dx.doi.org/10.1590/0001-3765201620150345 www.scielo.br/aabc What the largest tadpole feeds on? A detailed analysis of the diet composition of Pseudis minuta tadpoles (Hylidae, Dendropsophini) SÔNIA HUCKEMBECK2, LÍVIA T. ALVES2, DANIEL LOEBMANN2 and ALEXANDRE M. GARCIA1 1Instituto de Oceanografia, Universidade Federal do Rio Grande/ FURG, Av. Itália, Km 8, Carreiros, 96203-900 Rio Grande, RS, Brasil 2Instituto de Ciências Biológicas, Universidade Federal do Rio Grande/ FURG, Av. Itália, Km 8, Carreiros, 96203-900 Rio Grande, RS, Brasil Manuscript received on May 18, 2015; accepted for publication on August 10, 2015 ABSTRACT We analyzed the diet of 25 individuals of Pseudis minuta tadpoles which consisted in debris with more than 30%, follow by diatoms, euglenids, green algae, and desmids. With regard to the feeding strategy, P. minuta tadpoles are generalist consumer. The negative correlation between the abundance of items in the digestive tract and the mouth width indicate an effect of metamorphosis on the diet. Key words: algae, anuran, metamorphosis, trophic ecology. INTRODUCTION taxonomy (e.g. Barrio 1970, De Sá and Lavilla 1997, Kwet 2000), there is little information Neotropical frogs from the genera Pseudis on the trophic ecology of the larvae (Arias et al. encompass those hylids species most adapted to 2002, Vera-Candioti 2007). Consequently, little is live in aquatic environments (Huckembeck et al. known about the role species of tadpoles in aquatic 2014). The most conspicuous feature of this genus, environments (Santos et al. -
Satellite DNA Mapping in Pseudis Fusca (Hylidae, Pseudinae) Provides New Insights Into Sex Chromosome Evolution in Paradoxical Frogs
G C A T T A C G G C A T genes Article Satellite DNA Mapping in Pseudis fusca (Hylidae, Pseudinae) Provides New Insights into Sex Chromosome Evolution in Paradoxical Frogs Kaleb Pretto Gatto 1,* , Karin Regina Seger 1, Paulo Christiano de Anchieta Garcia 2 and Luciana Bolsoni Lourenço 1,* 1 Laboratory of Chromosome Studies, Department of Structural and Functional Biology, Institute of Biology, University of Campinas, Campinas 13083-863, SP, Brazil; [email protected] 2 Department of Zoology, Institute of Biological Sciences, Federal University of Minas Gerais, Belo Horizonte 31270-901, MG, Brazil; [email protected] * Correspondence: [email protected] (K.P.G.); [email protected] (L.B.L.); Tel.: +55-19-35216108 (L.B.L.) Received: 24 December 2018; Accepted: 8 February 2019; Published: 19 February 2019 Abstract: In the frog genus Pseudis, previous works found a sex-linked heteromorphism of the PcP190 satellite DNA in the nucleolus organizer region (NOR)-bearing chromosome pairs of Pseudis bolbodactyla and Pseudis tocantins, which possess a ZZ/ZW sex determination system. A pericentromeric inversion was inferred to have occurred during W chromosome evolution, moving a chromosomal cluster enriched by the PcP190 from the short arm (as observed in P. bolbodactyla) to the NOR-bearing long arm (as observed in P. tocantins). However, whether such an inversion happened in P. tocantins or in the common ancestor of Pseudis fusca and P. tocantins remained unclear. To assess this question, we mapped PcP190 in the karyotype of P. fusca from three distinct localities. Southern blotting was used to compare males and females. -
1704632114.Full.Pdf
Phylogenomics reveals rapid, simultaneous PNAS PLUS diversification of three major clades of Gondwanan frogs at the Cretaceous–Paleogene boundary Yan-Jie Fenga, David C. Blackburnb, Dan Lianga, David M. Hillisc, David B. Waked,1, David C. Cannatellac,1, and Peng Zhanga,1 aState Key Laboratory of Biocontrol, College of Ecology and Evolution, School of Life Sciences, Sun Yat-Sen University, Guangzhou 510006, China; bDepartment of Natural History, Florida Museum of Natural History, University of Florida, Gainesville, FL 32611; cDepartment of Integrative Biology and Biodiversity Collections, University of Texas, Austin, TX 78712; and dMuseum of Vertebrate Zoology and Department of Integrative Biology, University of California, Berkeley, CA 94720 Contributed by David B. Wake, June 2, 2017 (sent for review March 22, 2017; reviewed by S. Blair Hedges and Jonathan B. Losos) Frogs (Anura) are one of the most diverse groups of vertebrates The poor resolution for many nodes in anuran phylogeny is and comprise nearly 90% of living amphibian species. Their world- likely a result of the small number of molecular markers tra- wide distribution and diverse biology make them well-suited for ditionally used for these analyses. Previous large-scale studies assessing fundamental questions in evolution, ecology, and conser- used 6 genes (∼4,700 nt) (4), 5 genes (∼3,800 nt) (5), 12 genes vation. However, despite their scientific importance, the evolutionary (6) with ∼12,000 nt of GenBank data (but with ∼80% missing history and tempo of frog diversification remain poorly understood. data), and whole mitochondrial genomes (∼11,000 nt) (7). In By using a molecular dataset of unprecedented size, including 88-kb the larger datasets (e.g., ref. -
Advertisement Calls of Three Anuran Species (Amphibia) from the Cerrado, Central Brazil
South American Journal of Herpetology, 6(2), 2011, 67-72 © 2011 Brazilian Society of Herpetology ADVERTISEMENT CALLS OF THREE ANURAN SPECIES (AMPHIBIA) FROM THE CERRADO, CENTRAL BRAZIL ROGÉRIO P. BASTOS1, LUCIANA SIGNORELLI2,ALESSANDRO R. MORAIS2,5, TAÍS B. COSTA1, LEÔNCIO P. LIMA3, AND JOSÉ P. POMBAL JR.4 1 Departamento de Ecologia, ICB, UFG. Caixa Postal 131, CEP 74001-970, Goiânia, GO, Brasil. 2 Programa de Pós-Graduação em Ecologia e Evolução, ICB, UFG. Caixa Postal 131, 74001-970, Goiânia, GO, Brasil. E-mail: [email protected] 3 Instituto Chico Mendes de Conservação da Biodiversidade, CEP 74605-090, Goiânia, GO, Brasil. 4 Departamento de Vertebrados, Museu Nacional, UFRJ. CEP 20940-040, Rio de Janeiro, RJ, Brasil. 5 Corresponding author. ABSTRACT. Aspects of natural history, such as the advertisement call, of many frog species from central Brazil are unknown. This kind of vocalization is important for specific recognition, thus studies describing these calls are needed. Herein we describe the advertisement calls of three anuran species from the Cerrado Biome: (a) Allobates goianus (Aromobatidae); (b) Odontophrynus salvatori (Cycloramphidae); (c) Lysapsus caraya (Hylidae). From October to December/2001 and March/2009, the vocalizations of individuals of these species were recorded in three municipalities in Goiás state: Alto Paraíso, Araguapaz and Silvânia. The advertisement calls emitted by A. goianus presented modulation of frequency and those vocalizations emitted by O. salvatori and L. caraya showed pulsioned structure. In general, these species presented advertisement calls different from those emitted by other species in the same genus. This difference reinforces the importance of the advertisement calls for specific recognition and also the validity of these species. -
Leptodactylus Chaquensis (Anura, Leptodactylidae) As a Predator of Pseudis Platensis (Anura, Hylidae) in Southern Brazil
Lundiana International Journal of Biodiversity 12(1): 45-48. 2016. ISSN 1676-6180 © 2016 Instituto de Ciências Biológicas - UFMG Short Communication Leptodactylus chaquensis (Anura, Leptodactylidae) as a predator of Pseudis platensis (Anura, Hylidae) in southern Brazil Fabrício Hiroiuki Oda1,2*, Priscilla Guedes Gambale3 & Vinicius Guerra Batista3 1- Universidade Estadual de Maringá (UEM), Núcleo de Pesquisas em Limnologia, Ictiologia e Aqüicultura (Nupélia), Laboratório de Ictioparasitologia, Maringá, PR, Brazil. 2- Bolsista Pós-Doutorado Júnior (PDJ/CNPq). 3- Universidade Estadual de Maringá (UEM), Programa de Pós-Graduação em Ecologia de Ambientes Aquáticos Continentais (PEA). Maringá, PR, Brazil. *Corresponding author: [email protected] Abstract Frogs from the Family Leptodactylidae are among the most important opportunistic feeders on other anuran species. Here we report a case of predation of Pseudis platensis by the Cei’s white-lipped frog Leptodactylus chaquensis in breeding habitat from agricultural landscape, southern Brazil. Keywords: aquatic frog, breeding season, opportunistic predation, prey, terrestrial frog. Large and medium-sized anuran species temporary aquatic habitats of open areas are carnivorous, generalists and opportunistic (Uetanabaro et al. 2008, Oda et al. 2014). feeders that consume various prey items including their own or other species of Species of Pseudis are small and amphibians (Wells 2007, Santos & Vaz-Silva medium-sized aquatic frogs distributed from 2012). Among the Anura some of the most Guianas, northeastern Venezuela, Trinidad, important opportunistic feeders are species central to southern Brazil, Paraguay, from the Family Leptodactylidae (Toledo et al. southeastern Peru, eastern Bolivia, northeastern 2007). Argentina, and Uruguay (Frost 2014). This genus currently includes seven valid species Belonging to the L. -
Pseudis Paradoxa (Paradoxical Frog)
UWI The Online Guide to the Animals of Trinidad and Tobago Ecology Pseudis paradoxa (Paradoxical Frog) Family: Hylidae (Tree Frogs) Order: Anura (Frogs and Toads) Class: Amphibia (Amphibians) Fig. 1. Paradoxical frog, Pseudis paradoxa. [http://cdn-1.itsnature.org/wp-content/uploads/2010/06/14707595_437312.jpg, downloaded 29 March 2015] TRAITS. The adults’ heads are small compared to their bodies which are short and plump. Round and short snouts are also seen. Their eyes are yellow with a transverse brown bar, and are in a dorsolateral position on their heads. The fingers are free but the toes are webbed. Colour: Dorsal surface is green all through the anterior section of the body and brown along the back end of the body with dark spots (Fig. 1). The ventral surface has a whitish appearance with brown spots. There are also about three or four brown lines that connect near the thighs (Lescure and Marty 2000). Their croak sounds similar to a pig’s oink (Curious Creatures 2010). The tadpoles of the species are approximately 25cm long (Fig. 2) and the adults shrink to about 6.5-7.5cm UWI The Online Guide to the Animals of Trinidad and Tobago Ecology (Emerson 1988; Lescure and Marty 2000). This reduction of size from the tadpole to the sexually mature adult (Fig. 3) is how the species received its name. Tadpoles early in their lifecycle have a vertical stripe pattern along their bulk that helps in predator avoidance. They lose this striping as they grow (Sergeant 2011). DISTRIBUTION. It is found in some of the South American countries (Fig.