622<strong>Threatened</strong> <strong>Amphibian</strong>s of the WorldBibliography: Acosta-Galvis, A.R. (2000), Cochran, D.M. and Goin, C.J. (1970), Lynch, J.D. (1976b), Lynch, J.D. and Duellman, W.E.(1997), Lynch, J.D., Ruiz-Carranza, P.M. and Ardila-Robayo, M.C. (1994), Lynch, J.D., Ruiz-Carranza, P.M. and Ardila-Robayo, M.C. (1997),Ruiz-Carranza, P.M., Ardila-Robayo, M.C. and Lynch, J.D. (1996)Data Providers: Martha Patricia Ramírez Pinilla, Mariela Osorno-Muñoz, Jose Vicente Rueda, Adolfo Amézquita, María CristinaArdila-RobayoEleutherodactylus tayrona Lynch and Ruíz-Carranza, 1985This species is known from the Sierra Nevada de Santa Marta, in the departments of Cesar, Guajira and Magdalena,Colombia, from 1,300-2,700m asl. It is extremely abundant. This is a nocturnal species that can be observed perchingon arboreal bromeliads, in which it shelters during the day. Breeding is by direct development, and the eggs are alsolaid on arboreal bromeliads. The major threats to this species’ habitat are cultivation and fumigation of crops, andthe rearing of livestock. Its range includes Parque Nacional Natural Sierra Nevada de Santa Marta.Bibliography: Acosta-Galvis, A.R. (2000), Cochran, D.M. and Goin, C.J. (1970), Lynch, J.D. and Ruiz-Carranza, P.M. (1985a), Ruiz-Carranza,P.M., Ardila-Robayo, M.C. and Lynch, J.D. (1996)Data Providers: Martha Patricia Ramírez Pinilla, Mariela Osorno-Muñoz, Jose Vicente Rueda, Adolfo Amézquita, María CristinaArdila-RobayoEleutherodactylus vanadise La Marca, 1984This species is known from La Mucuy, Monterey, Monte Zerpa and the Bosque de San Weusebio, in Mérida State,in the Venezuelan Andes, from 1,800-2,600m asl. It is a common species. It lives in bushes and on the ground incloud forests and secondary forests. Breeding is by direct development. Its habitats are not seriously threatenedat present, and much of its range is in protected areas. Some populations are within Parque Nacional Sierra de LaCulata and Parque Nacional Sierra Nevada.Bibliography: Barrio Amorós, C.L. (2004), Frost, D.R. (1985), La Marca, E. (1984), La Marca, E. (1992), La Marca, E. (1997)Data Providers: Enrique La Marca, Juan Elías García-PérezEleutherodactylus vicarius Lynch and Ruíz-Carranza, 1983This species is known from the departments of Huila, Nariño and Cauca, on the east slope of the highlands of theCordillera Central, Colombia, from 2,900-3,275m asl. It is common. This nocturnal species occurs on vegetation upto 1.5m above ground, inside the forest as well as next to streams. During the day it can be found under rocks andlogs, and it is also found in páramo vegetation. Breeding is by direct development. The major threat to this species ishabitat loss, in particular in Nariño Department, caused by logging and agricultural development for crop cultivation(including illegal crops) and rearing of livestock. Other high-altitude, stream-breeding Eleutherodactylus specieshave undergone declines possibly due to chytridiomycosis, so this might be a potential future threat. The range ofthe species includes Parque Nacional Natural Puracé. Given the possible threat of chytridiomycosis this speciesshould be monitored carefully.Bibliography: Acosta-Galvis, A.R. (2000), Lynch, J.D. and Duellman, W.E. (1997), Lynch, J.D. and Ruiz-Carranza, P.M. (1983), Lynch, J.D.,Ruiz-Carranza, P.M. and Ardila-Robayo, M.C. (1997), Ruiz-Carranza, P.M., Ardila-Robayo, M.C. and Lynch, J.D. (1996)Data Providers: Fernando Castro, Maria Isabel Herrera, John LynchEleutherodactylus viridis Ruíz-Carranza, Lynch and Ardila-Robayo, 1997This species is known from three localities in the western part of Antioquia Department, on the western and easternslopes of the Cordillera Occidental, and from one locality in northern Antioquia Department, on the northern face ofthe Cordillera Occidental, Colombia, between 1,480 and 1,940m asl, It is an uncommon species. It is restricted tovery humid forests, and occurs on Araceae vegetation and ferns, up to 1.5m above the ground. Breeding is by directdevelopment. There are no threats to the species’ habitat at present as its known range is wholly within two parks.Three of the localities in which it occurs are within Parque Nacional de Las Orquídeas, and the fourth is in ParqueNacional Natural Paramillo.Bibliography: Acosta-Galvis, A.R. (2000), Lynch, J.D. (1998b), Lynch, J.D., Ruiz-Carranza, P.M. and Ardila-Robayo, M.C. (1997), Paez,V.P. et al. (2002), Ruiz-Carranza, P.M., Lynch, J.D. and Ardila-Robayo, M.C. (1997)Data Providers: Fernando Castro, Maria Isabel Herrera, John LynchEupsophus roseus (Duméril, Bibron, 11841)This species is known from 38°S to 40°S in Cautín and Valdivia Provinces, Chile, from 50-1,000m asl. It is locallycommon. This species can be found under logs close to swamps or streams in temperate Nothofagus forest, and itmay persist in fairly disturbed areas. Eggs are deposited in small, water-filled holes on hillsides. The major threat tothis species is habitat destruction caused by wood extraction and establishment of pine and eucalyptus plantations. Inthe northern part of its range it is threatened by forest fires. It occurs in Parque Nacional Tolhuaca and the MonumentoNatural Cerro Ñielol. Legislation to protect the Nothofagus forest habitat is needed.Taxonomy: Specimens from Argentina formerly referred to this species belong to Eupsophus calcaratus (E. Lavilla pers. comm.).Bibliography: Formas, J.R. (1995), Núñez, J.J., Zárraga, A.M. and Formas, J.R. (1999), Servicio Agrícola Ganadero (1998), Veloso, A.and Navarro, J. (1988)Data Providers: Alberto Veloso, Herman Núñez, Jose Núñez, Juan Carlos OrtizEupsophus vertebralis Grandison, 1961This species occurs in the lake region of Chile, approximately from 40°S to 44°S, and from a single locality in Argentina(Puerto Blest, Río Negro Province). Its altitudinal range is from 50-1,000m asl. It is uncommon even in suitable habitats.In Chile it was recorded as recently as November 2002, but there have been no records for Argentina since 1973. Thisspecies is found under large logs and rocks near streams in temperate Nothofagus forest. Eggs are deposited in small,water-filled holes on hillsides. The major threat to this species is habitat destruction caused by wood extraction andestablishment of pine and eucalyptus plantations. It occurs in Parque Nacional Tolhuaca and Parque Natural AlerceCostero in Chile. In Argentina, it occurs in Parque Nacional Nahuel Huapi. There is a need for improved legislationto protect remaining tracts of Nothogagus forest in the range of this species.Bibliography: Basso, N.G. and Ubeda, C.A. (1999), Formas, J.R. (1989), Formas, J.R. (1991), Formas, J.R. (1992), Formas, J.R. (1993),Formas, J.R. (1994), Formas, J.R. (1995), Lavilla, E.O. et al. (2000), Lavilla, E.O., Barrionuevo, S. and Baldo, D. (2002), Servicio AgrícolaGanadero (1998), Veloso, A. and Navarro, J. (1988)Data Providers: Alberto Veloso, Herman Núñez, Jose Núñez, Juan Carlos Ortiz, Carmen ÚbedaGastrotheca andaquiensis Ruíz-Carranza and Hernández, 1976This species occurs on the Amazonian slopes of the Andes in southern Colombia (in Caquetá, Huila, and PutumayoDepartments) and in Ecuador south to Zamora Province, at 1,000-2,000m asl. It is a moderately common species. It isarboreal, living on the vegetation next to water sources inside cloud forest. There is a record of an individual observedin a flat area on a ridge, with a relatively open canopy and many tree falls, but otherwise there is no information on itsadaptability to secondary habitats. The eggs are carried in a pouch on the female’s back, where they develop directlywithout a larval stage. The major threats are deforestation due to smallholder livestock ranching and cultivation ofcrops (including some illegal crops), logging, and human settlement, and pollution resulting from the spraying ofillegal crops. In Ecuador, its geographic range overlaps with the Reserva Ecológica Cayambe-Coca and the ReservaEcológica Antisana, and Parque Nacional Sumaco Napo-Galeras, Parque Nacional Llanganates, and Parque NacionalSangay. It is not known from any protected areas in Colombia.Taxonomy: This genus has recently been moved from the family Hylidae (Faivovich et al. 2005).Bibliography: Duellman, W.E. (1989a), Duellman, W.E. and Lynch, J.D. (1988), Duellman, W.E., Maxson, L.R. and Jesiolowski, C.A.(1988), Faivovich, J. et al. (2005), Ruiz-Carranza, P.M. and Hernández-Camacho, J.A. (1976a), Ruiz-Carranza, P.M., Ardila-Robayo, M.C.and Lynch, J.D. (1996)Data Providers: Wilmar Bolívar, Luis A. Coloma, Santiago RonGastrotheca aureomaculata Cochran and Goin, 1970This species is known from the departments of Cauca and Huila on the eastern slopes of the Cordillera Central insouth-central Colombia, from 2,000-2,600m asl. This is a common species. It is arboreal, occurring on vegetationalongside streams in Andean forests. It has also been recorded from relatively disturbed areas such as in trees infarmers’ gardens. Its main requirement is dense vegetation. The eggs develop in a pouch on the back of the femaleand then the larvae are transported to small pools where they develop further. A major threat resulting in destructionof its habitat is the cultivation of illegal crops. Water pollution is also a threat. The range of the species does notinclude any protected areas. More research into its extent of occurrence is needed, and establishment of a protectedarea for this species would be advisable.Taxonomy: This genus has recently been moved from the family Hylidae (Faivovich et al. 2005).Bibliography: Cochran, D.M. and Goin, C.J. (1970), Duellman, W.E. (1989a), Faivovich, J. et al. (2005)Data Providers: Fernando Castro, John LynchHemiphractus bubalus (Jiménez de la Espada, 1871)This species occurs in the lower Amazonian slopes of the Andes in Ecuador, Peru and Colombia (Caquetá to Putumayo),from 300-2,000m asl. It is a rare species. Individuals have been found in dense cloud forests where it favours perches,being found on the branches of bushes and small trees (Trueb 1974). At Cordillera del Cutucú, Ecuador, specimenshave been collected in very wet forest, where the ground and most trees were covered with moss (Duellman andLynch 1988); it was also collected at the same habitat type in Peru. It is not present in modified habitats. This speciesreproduces by direct development and the eggs are carried in a pouch on the female’s back. It is probably a specializedpredator on other frog species that only survives in areas of high frog density. This species is threatened by forestloss due to infrastructure development for human settlements, logging, and agricultural development (including forthe cultivation of crops and the rearing of livestock). Although much forest habitat remains within the range of thisspecies, it is very sensitive to slight habitat alteration and the rate of forest loss within the majority of its range (theEcuadorian portion) is very high. Its geographic range overlaps with the Reserva Ecológica Cayambe-Coca, ParqueNacional Sumaco Napo-Galeras, and Parque Nacional Sangay, in Ecuador. In Peru it is present in the Zona ReservadaSantiago-Comaina.Taxonomy: This genus has recently been moved from the family Hylidae (Faivovich et al. 2005).Bibliography: Duellman, W.E. and Lynch, J.D. (1988), Faivovich, J. et al. (2005), Jiménez de la Espada, M. (1871), Reynolds, R. andIcochea, J. (1997), Trueb, L. (1974)Data Providers: Luis A. Coloma, Santiago Ron, Diego Cisneros-Heredia, Fernando Castro, Jose Vicente RuedaHemiphractus fasciatus Peters, 1862This species occurs through much of the central and eastern cordilleras of Panama, south through the Pacific slopesof Colombia (in Antioquia and Cauca Departments, and almost certainly more widely) and the northern slopes ofthe western and central cordilleras, to north-western Ecuador (south to the Guajalito Protection Forest in PichinchaProvince). It is known only from a small number of localities within its overall range, from 300-2,000m asl. This is avery rare species. Its habitat is very humid lowland, lower montane and cloud forests; it inhabits primary forest only.By day, individuals have been found in leaf-litter on the forest floor, whereas by night they favour perches above theground. It lives only in areas of high frog densities, since it preys on other frogs. Breeding is by direct development;the eggs are carried on the back of the female. The major threats are deforestation due to agricultural development(including cultivation of illegal crops), logging, and human settlement, and pollution resulting from the spraying ofillegal crops. It has been recorded from Parque Internacional La Amistad, the Reserva Forestal Fortuna, and ParqueNacional Darién in Panama. In Ecuador, its geographic range overlaps with the Reserva Ecológica Cotacachi-Cayapas.It is not known from any protected areas in Colombia.Taxonomy: This genus has recently been moved from the family Hylidae (Faivovich et al. 2005).Bibliography: Duellman, W.E. (2001), Faivovich, J. et al. (2005), Ibáñez, R. et al. (2000), Peters, W.C.H. (1862), Ruiz-Carranza, P.M.,Ardila-Robayo, M.C. and Lynch, J.D. (1996), Trueb, L. (1974), Young, B. et al. (1999)Data Providers: Luis A. Coloma, Santiago Ron, Karl-Heinz Jungfer, Frank Solís, Roberto Ibáñez, César Jaramillo, Querube FuenmayorLepidobatrachus asper Budgett, 1899This species is known from the Chaco of Paraguay (in Central, Presidente Hayes, and Alto Paraguay Departments) andnorthern Argentina (in Chaco, Cordoba, Corrientes, Formosa, Santa Fe, and Santiago del Estero Provinces). In Paraguayit occurs up to 200m asl. It is a common species in Paraguay but is very rare in Argentina, where it was last collectedin 1986. Extensive work in an area in Cordoba where it was once recorded has not turned up any recent specimens.It inhabits dry scrubland and semi-arid areas, and breeds in temporary pools and water tanks on cattle farms. InArgentina, it occurs in vegetation near saline lakes. During the dry season individuals burrow underground and waitfor rains before emerging again. The breeding season is short and larval development is rapid. This species can bethreatened by fires, and potentially also by over-grazing by livestock. Its range includes Parque Nacional Defensoresdel Chaco in Paraguay, although it is not known from any protected areas in Argentina.Bibliography: Aquino, A.L., Scott, N.J. and Motte, M. (1996), Di Tada, I.E. et al. (1996)Data Providers: Lucy Aquino, Ismael di Tada, Julian FaivovichLeptodactylus laticeps Boulenger, 1918This species occurs in the Gran Chaco of Paraguay, Bolivia and Argentina, from 0-300m asl. It is common in parts ofParaguay and Bolivia but is rare in Argentina due to over-harvesting for the international pet trade. It is a terrestrialspecies of open habitats that breeds in temporary ponds. It probably does not adapt well to anthropogenic disturbance.Over-harvesting for the international pet trade is a major threat. It is collected in Paraguay and Argentina, and eachadult is worth $300-$600. It does occur in several protected areas, but monitoring of its population status is needed,and there is a need to ensure that harvesting of this species from the wild is managed in a sustainable manner.Bibliography: Alvarez, B.B. et al. (2002), Alvarez, B.B. et al. (2003), Aquino, A.L., Scott, N.J. and Motte, M. (1996), De la Riva, I. et al.(2000), Frost, D.R. (1985), Köhler, J. (2000a)Data Providers: Claudia Cortez, Steffen Reichle, Lucy Aquino, Ismael di Tada
<strong>Near</strong> <strong>Threatened</strong> <strong>Amphibian</strong> <strong>Species</strong> 623Phyllonastes lochites (Lynch, 1976)This species is known from moderate altitudes on the Amazonian slopes of the Andes from the Cordillera del Cóndorin Peru, and the Cordillera de Cutucú in Ecuador (in Pastaza, Zamora Chinchipe, and Morona Santiago Provinces). Ithas an altitudinal rage of 900-1,700m asl. It was recently recorded from the Alfonso Ugarte military post in AmazonasDepartment, Cordillera del Cóndor, Peru, at 1,138m asl. It is rarely encountered, possibly due to its secretive habits.The holotype was collected during the day in leaf-litter in cloud forest (Lynch 1976d), and it also occurs in old growthand secondary forest. Reproduction occurs via direct development. Its range in the Cordillera del Cóndor is not significantlythreatened since people are averse to entering the area due to the land mines left during the Ecuador-Peruborder war in 1995. Its geographic range overlaps Parque Nacional Sangay in Ecuador.Bibliography: Almendariz, A. (1997), Lynch, J.D. (1976d)Data Providers: Diego Cisneros-Heredia, Ana Almandáriz, Jorge Luis Martinez, Daniel Neirapresent in the muddy bottoms of streams. There is no information on its breeding biology, though it presumablytakes place by larval development in streams. It is affected by ongoing habitat loss and degradation, as a result oflogging and agricultural expansion. It is also threatened by water pollution and aquaculture. Despite these threatsits populations appear to be currently stable. However, chytridiomycosis is a potential future threat that could causeserious declines, but this has not yet been confirmed in this species. It occurs in Parque Nacional y Área Natural deManejo Integrado Cotapata, and Área Natural de Manejo Integrado Nacional Apolobamba. Given the possible threatof chytridiomycosis, this species should be monitored closely.Taxonomy: This species was formerly considered to be a synonym of Telmatobius marmoratus (Vellard 1970). It was resurrected as afull species by De la Riva et al. (2000). T. ifornoi is included as a synonym of this species, following De la Riva (2004).Bibliography: De la Riva, I. (2004), De la Riva, I. et al. (2000), Lavilla, E. and Ergueta, P. (1995), Lavilla, E. and Ergueta, P. (1999),Vellard, J. (1970)Data Providers: Claudia Cortez, Steffen Reichle, Ignacio De la Riva, Jörn KöhlerPleurodema bibroni Tschudi, 1838FOUR-EYED FROGTelmatobius jelskii (Peters, 1873)This species is known from Uruguay (in the departments of Canelones, Florida, Lavalleja, Maldonado, Montevideo,Rocha, San José and Treinta y Tres, Artigas, Durazno, and Río Negro) and from Brazil (Rio Grande do Sul), from 0-1,100masl. This species is rare and occurs in widely scattered populations. It is probably extinct in Montevideo Departmentbecause of habitat destruction. It occurs in coastal sand plains, open savannahs, rocky outcrops, grasslands and openmontane habitats, and probably does not tolerate habitat disturbance. Breeding takes place in temporary pools. Themain threat is habitat destruction due to encroaching cultivation of crops, establishment of pine plantations, andencroaching human settlements. It occurs in Floresta Nacional de São Francisco de Paula.Taxonomy: This form is probably a complex of more than one species. It was long confused with Pleurodema thaul, until the work ofDonoso-Barros (1969).Bibliography: Braun, C.A.S. (1973), Braun, P.C. and Braun, C.A.S. (1980), Klappenbach, M.A. and Langone, J.A. (1992), Langone, J.A.(1994), Lavilla, E.O. et al. (2000), Maneyro, R. and Langone, J.A. (2001)Data Providers: Débora Silvano, Esteban Lavilla, Paulo Garcia, Jose LangonePleurodema kriegi (Müller, 1926)This species is endemic to the Pampa de Achala, Cordoba Province, Argentina, from 1,800-2,600m asl. It is abundantwithin its small range, although it is seen only during the breeding season. It occurs in montane grasslands and associatedrocky outcrops. Adults live under rocks or in abandoned rodent holes outside the breeding season. It reproducesexplosively during the first rains in November and December. Pairs spin a gelatinous nest attached to vegetation intemporary pools, or sometimes in backwater pools of streams. Significant threats to this species have previouslyincluded extensive cattle ranching and the associated alteration of water sources. However, the recent declarationof protected areas within its range means that the future of this species now looks much more secure. It occurs inParque Nacional Quebrada del Condorito and the Reserva Hídrica Provincial de Pampa de Achala.Bibliography: Di Tada, I.E. et al. (1996), Lavilla, E.O. et al. (2000), Lavilla, E.O. and Cei, J.M. (2001)Data Providers: Esteban Lavilla, Ismael di TadaProceratophrys bigibbosa (Peters, 1872)This species is known from the Rio Grande do Sul, Brazil, and central districts of Misiones Province, Argentina, from300-1,200m asl. It has never been recorded as being abundant, and one population in Sao Francisco de Paula hasdisappeared. It inhabits Araucaria forests in mountainous regions, and breeds in small streams. Outside the breedingseason it occurs in leaf-litter. The eggs may be deposited under stones on streambeds. A major threat to this speciesis habitat loss due to deforestation, for smallholder livestock ranching, and the establishment of pine plantations.It is also threatened by pollution of soil and water due to agricultural practices and industrial pollution with organicwastes. This species’ range overlaps with several protected areas.Taxonomy: Proceratophrys palustris is similar to this species.Bibliography: Kwet, A. and Di-Bernardo, M. (1999), Kwet, A. and Faivovich, J. (2001), Lavilla, E.O. et al. (2000), Lavilla, E.O. and Cei,J.M. (2001)Data Providers: Débora Silvano, Axel Kwet, Paulo Garcia, Julian FaivovichRupirana cardosoi Heyer, 1999This species is restricted to the region of Chapada Diamantina, in the northern part of the Espinhaço Range in thestate of Bahia, eastern Brazil, at around 1,200m asl. This species is common within its small range. It lives on thebanks of small streams with white sand and rocks, in high-altitude grassy vegetation, and breeds in temporary streamsand ponds. The major threats are habitat loss due to expanding cultivation of crops and livestock grazing, and fire. Itoccurs in Parque Nacional Chapada da Diamantina.Bibliography: Heyer, W.R. (1999)Data Providers: Flora Junca, Débora SilvanoStefania satelles Señaris, Ayarzaguena and Gorzula, 1997 “1996”This species is known from Aprada tepui (tepuis are Venezuelan flat top mountains) at 2,500m asl, and from Angasimatepui (Adanta) and Upuigma tepui (El Castillo), from between 2,000 and 2,100m asl. The mountain chains ofAngasima tepui and Upuigma tepui are not physically connected, and lie about eight to 10km apart. Aprada tepuiis likewise separated from the Chimantá massif, and lies about 20km to the north-east of it. This species thereforehas a disjunct distribution. It is common on these summits. This is a nocturnal frog found on open, rocky surfaces,and in crevices and depressions close to watercourses. It carries its eggs and juveniles on its back, and breeds bydirect development. There are no known threats to the species’ habitat at present. This species occurs within ParqueNacional Canaima. In addition, Venezuelan flat top mountains (tepuis) are protected by law, so all the species occurringon them are protected.Taxonomy: This genus has recently been moved from the family Hylidae (Faivovich et al. 2005). Some specimens of this speciesresemble Stefania ginesi, but in these cases their general aspect is that of a somewhat slimmer and slightly smaller frog. Specimensfrom Terekeyuren (Murisipan) tepui and Kamarkawarai tepui, from the Los Testigos massif, closely resemble S. satelles, but were notassigned to this species pending further specimens becoming available.Bibliography: Barrio, C. (1998), Duellman, W.E. and Hoogmoed, M.S. (1984), Faivovich, J. et al. (2005), La Marca, E. (1997), MacCulloch,R.D. and Lathrop, A. (2002), Señaris, J.C., Ayarsagüena, J. and Gorzula, S. (1997)Data Providers: Celsa Señaris, Enrique La MarcaTelmatobius bolivianus Parker, 1940This species is known from much of the central Andes in Peru (from the departaments of Ayacucho, Huancavelica andJunín), from 2,700-4,500m asl. It was previously common, but has undergone declines. It is a semi-aquatic riparianfrog, and may be found in muddy beds of streams among shrublands and grasslands. It has been found in ditches onarable land. Breeding takes place in streams. This species is locally affected by harvesting for both food and traditionalmedicine, and by water pollution (from agrochemicals and domestic waste). Telmatobius populations living at highaltitudes might be particularly prone to becoming infected with chytridiomycosis, although this disease has yet to bereported from this species. It might be present in the Reserva Chacamarca although this requires confirmation. There isa need to regulate its harvesting and to reduce the local water pollution. Given the possible threat of chytridiomycosisthis species should be monitored closely.Bibliography: Rodríguez, L.O., Cordova, J.H. and Icochea, J. (1993), Sinsch, U. (1986), Sinsch, U. (1990), Sinsch, U., Salas, A.W. andCanales, V. (1995)Data Providers: Javier Icochea, Ulrich Sinsch, Edgar LehrTelmatobius simonsi Parker, 1940This species is endemic to the Bolivian Andes, where it has been recorded from the departments of Chuquisaca,Cochabamba and Santa Cruz (Köhler 2000a), from 1,000-2,800m asl. It is locally common, although it is apparently indecline. It is an aquatic species, occurring in both open and forest habitats, in inter-Andean valleys. It can be foundat night by the sides of roads, in waterways or trenches, or in ponds and small streams (Köhler 2000a). There is noinformation on its breeding biology, though it presumably takes place by larval development in water. It is probablydeclining because of water pollution, and habitat loss and degradation due to agricultural development, logging, andlivestock grazing. Telmatobius populations living at higher altitudes might be particularly prone to becoming infectedwith chytridiomycosis, so this disease might be a potential threat for this species in the future. It occurs in ParqueNacional El Palmar and Parque Nacional Amboró. Given the possible threat of chytridiomycosis there is a need forclose monitoring of the population status of this species.Taxonomy: Populations from the La Siberia area, previously considered to belong to Telmatobius simonsi, have recently been describedas T. sibiricus (De la Riva and Harvey 2003).Bibliography: De la Riva, I. and Harvey, M.B. (2003), Köhler, J. (2000a), Parker, H.W. (1940)Data Providers: Claudia Cortez, Steffen Reichle, Ignacio De la Riva, Jörn KöhlerThoropa saxatilis Cocroft and Heyer, 1988This species occurs in the southernmost part of the Atlantic forest in the states of Santa Catarina and Rio Grandedo Sul, southern Brazil, from 300-1,000m asl. It is rarely collected, although it was found in 2001, and it appearsto have disappeared from some localities. This species lives in forested areas on rocky cliffs; eggs are depositedunder waterfalls on rocks. Some populations of this species have been affected by changes in watercourses, andby sedimentation caused by road construction, as well as by general forest loss. However, these factors do notfully account for the recorded declines. Like amphibians in some other parts of the wet tropics, it appears to havedisappeared from areas of apparently suitable habitat, and chytridiomycosis cannot be ruled out as a threat, eventhough this disease has not yet been confi rmed from Brazil. This species occurs in Parque Nacional da Serra Geraland Parque Nacional de Aparados da Serra. Given the possible threat of chytridiomycosis, there is a need for closemonitoring of the population status of this species.Bibliography: Cocroft, R.B. and Heyer, W.R. (1988), Garcia, P.C.A. and Vinciprova, G. (1998)Data Providers: Paulo GarciaAdelotus brevis (Günther, 1863)LIMNODYNASTIDAETUSKED FROGThis Australian endemic has a disjunctive distribution, occurring in the Clarke Range (mid-eastern Queensland), thenfrom Shoalwater Bay (mid-eastern Queensland) south along the coast to Moss Vale (mid-eastern New South Wales),and inland to Blackdown Tableland and Carnarvon Gorge. It was formerly common across a broad altitudinal rangebut at present it is common only at altitudes of less than 400m asl. There is no information on the status of inlandpopulations of this species. Elswhere, it is now absent from some areas of apparently suitable habitat. For example,it has not been recorded along the Great Dividing Range in recent surveys. Upland populations in northern New SouthWales have also declined, and the species is listed as threatened in the region. There is no published informationon its overall population size, structure, genetics or dynamics. This species is found in wet forest and dry forestenvirons usually along streams, but also around dams. See Katsikaros and Shine (1997) for studies on diet, habitatuse, mating systems and sexual dimorphism. Breeding takes place in streams and ponds. Unpigmented eggs are laidin a foam nest hidden from the light, and development is usually complete within 71 days. The major threat to thisspecies is loss and degradation of its habitat through agricultural and urban development. Other significant threatsare the introduced predatory fi sh Gambusia holbrooki, and the spread of weeds. Dead frogs that have suffered fromchytridiomycosis have been found in south-eastern Queensland and north-eastern New South Wales. The range ofthe species includes several protected areas. Research into the spread of chytrid fungus and education on methodsof minimizing and preventing its spread is also needed as a conservation measure.Bibliography: Barker, J., Grigg, G. and Tyler, M. (1995), Czechura, G.V. (1986b), Hines, H., Mahony, M. and McDonald, K. (1999),Katsikaros, K. and Shine, R. (1997), Martin, A.A. (1967)Data Providers: Harry Hines, Ed Meyer, Jean-Marc Hero, David Newell, John ClarkeThis species is known only from the Yungas forests of La Paz Department, Bolivia, from 2,000-3,000m asl. Telmatobiusifornoi, known only from Chuspipata, in Nor Yungas Province, La Paz Department, at 3,050m asl, is now considered tobe a synonym (Lavilla and Ergueta 1999). This is the most common and widespread Telmatobius species in Bolivia.It is an aquatic species that occurs in fast-flowing rivers and streams in cloud forests and Yungas forest. It is often