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Introduction
Glassfrogs, anurans of the family Centrolenidae, have
received considerable attention during the last decade
(for a bibliographic review see Cisneros-Heredia and
McDiarmid, 2007). In particular, studies on the Glass-
frogs from the eastern slopes of the Andes and from the
Amazonian lowlands have revealed our lack of under-
standing of its diversity and distribution patterns (Cis-
neros-Heredia and McDiarmid, 2006a, 2006b, 2007;
Guayasamin et al., 2006; Cisneros-Heredia and Meza-
Ramos, 2007; Cisneros-Heredia et al., 2008). Herein we
present the rst country records of Hyalinobatrachium
iaspidiense from Ecuador and Peru that suggest a con-
tinuous distribution of this species across the Amazo-
nian basin.
Hyalinobatrachium iaspidiense is among the most
distinctive species of centrolenids by having a particu-
lar dorsal pattern only shared with Hyalinobatrachium
mesai (Cisneros-Heredia and McDiarmid, 2007; Barrio-
Amoros and Brewer-Carias, 2008). Both species show
large lime-green dorsal blotches that turn white when
individuals are preserved (Ayarzagüena, 1992; Lescure
and Marty, 2000; Señaris and Ayarzagüena, 2005; D.F.
Cisneros-Heredia, R.W. McDiarmid, J.P. Caldwell and
G. Rivas, pers. obs.). These marks are a unique colour
arrangement of the dorsal parietal peritoneum of centro-
lenids (Cisneros-Heredia and McDiarmid, 2007). The
most conspicuous difference between Hyalinobatra-
chium iaspidiense and H. mesai are the green bones of
the latter vs. white bones in the former.
Hyalinobatrachium iaspidiense was described based
on specimens collected at Quebrada Jaspe, state of
Bolivar, Guayana region of Venezuela (Ayarzagüena,
1992). Señaris and Ayarzagüena (2005) reported it from
Caño Colima on the slopes of Serranía de Imataca,
state of Bolivar, Venezuela. It has been reported as H.
nouraguense (a synonym, see below for details) in: four
localities in French Guiana (Lescure and Marty, 2000);
one in Guyana (Ernst, Rödel and Arjoon, 2005); four in
Suriname (Kok and Castroviejo-Fisher, 2008); and two
in Brazil (Cordeiro-Duarte et al., 2002; Caldwell and
Shepard, 2005). Thus, it has been reported so far only
from north-eastern areas of Amazonia.
Between 20th of May and 1st of June 2007 a male of
Hyalinobatrachium iaspidiense (DHMECN 04033,
Museo Ecuatoriano de Ciencias Naturales, Quito,
Ecuador; Fig. 1) was collected from the locality of
Totoa Nai’qui, Cofán-Dureno territory, province
of Sucumbíos, Republic of Ecuador (0.03442° S,
76.75278º W, ca. 280 m above sea level) by Mario
Yánez-Muñoz and Angel Chimbo. It was found on the
leaf of a bush directly over the water surface in a ooded
forest. This record represents the rst country record of
this species from Ecuador. Yánez-Muñoz and Chimbo
(2007) reported this specimen as “Hyalinobatrachium
sp. A” and Yánez-Muñoz and Cisneros-Heredia
(2008) as Hyalinobatrachium sp. N12”, commenting
that it was “apparently related or conspecic with
Hyalinobatrachium iaspidiense”.
Herpetology Notes, volume 2: 49-52 (2009) (published online on 06 May 2009)
New country records of Hyalinobatrachium iaspidiense (Amphibia,
Anura, Centrolenidae) from the Amazonian lowlands of Ecuador
and Peru
Mario Yánez-Muñoz1, Pedro Pérez-Peña2 and Diego Cisneros-Heredia*1,3,4
1 Museo Ecuatoriano de Ciencias Naturales, Sección Vertebra-
dos, División de Herpetología, calle Rumipamba No. 341 y
Ave. de Los Shyris, Quito, Ecuador.
2 Universidad Nacional de la Amazonía Peruana, calle Pevas
5ta Cuadra, Iquitos, Perú.
3 Universidad San Francisco de Quito, Colegio de Ciencias
Biológicas & Ambientales, calle Diego de Robles y Ave. In-
teroceánica, Campus Cumbayá, Edif. Maxwell, Casilla Postal
17-1200-841, Quito, Ecuador;
e-mail: diegofrancisco_cisneros@yahoo.com
4 King’s College London, Department of Geography, Strand,
London WC2R 2LS, United Kingdom.
* corresponding author
Abstract. We report the rst records of Hyalinobatrachium iaspidiense (Ayarzagüena, 1992) from Ecuador and Peru based on
voucher specimens collected in lowland Amazon rainforests. These are the westernmost records of this species and suggest a
continuous distribution across the entire Amazon basin.
Mario Yánez-Muñoz et al.
50
In November 2003 a female of Hyalinobatrachium
iaspidiense (MZUNAP 0517, Museo de Zoología,
Facultad de Ciencias Biológicas, Universidad Nacional
de la Amazonía Peruana, Iquitos, Peru; Fig. 2) was
collected at the Lago Preto-Paredón on the frontier
between Peru and Brazil in the province of Ramón
Castilla, department of Loreto, Republic of Peru
(4.46157° S, 71.75133° W, ca. 95 m above sea level)
by Pedro Pérez-Peña. The individual was found on the
leave of a shrub ca. 1.2 m above the ground and about
50 m away from a small lagoon in terra rme forest
dominated by Lepidocaryum tenue and represents
the rst record of this species from Peru. Pérez et al.
(2006) and Pérez (2007) regarded this specimen as
Hyalinobatrachium sp”.
Specimens DHMECN 04033 and MZUNAP 0517
show all diagnostic characteristics of Hyalinobatrachium
iaspidiense, including the dorsal coloration pattern,
white bones, transparent ventral parietal peritoneum and
most visceral peritonea covered by iridophores except
for the pericardium that is transparent; supporting their
specic identication.
These new records extend the known range of
Hyalinobatrachium iaspidiense nearly 1900 km from
the nearest known locality, the municipality of President
Figueiredo (state of Amazonas, Brazil) and represent
the westernmost record of this species suggesting that
H. iaspidiense is widely distributed across the entire
Amazonian lowlands (Fig. 3).
Ernst et al. (2005) as well as Cisneros-Heredia
and McDiarmid (2007) suggested synonymy of
Hyalinobatrachium iaspidiense and H. nouraguense
based on morphological characters. This hypothesis
was later supported by molecular data (Guayasamin
et al. 2007: Fig. 5 and 6) showing that almost no
differentiation between populations collected from
or near the respective type localities was evident. By
analysing the information presented by Ernst et al.
(2005), Cisneros-Heredia and McDiarmid (2007)
and Guayasamin et al. (2007) we treat both species
Figure 1. Hyalinobatrachium iaspidiense (DHMECN 04033) from the Cofán-Dureno territory, province of Sucumbíos, Republic
of Ecuador.
New records of H. iaspidiense from Ecuador and Peru 51
as conspecics of H. iaspidiense Ayarzagüena, 1992.
Cisneros-Heredia and McDiarmid (2007) reported
that H. nouraguensis and H. iaspidiense differed in
the condition of iridophores over the pericardium, but
a closer inspection showed that these differences are
preservation artefacts rather than valid intraspecic
differences (Lescure and Marty, 2000; Señaris
and Ayarzagüena, 2005; G. Rivas pers. comm.; S.
Castroviejo-Fisher pers. comm.). Cisneros-Heredia and
McDiarmid (2007) hypothesized that species with large
dorsal blotches of iridophores form a monophyletic
group but were uncertain about the relationships of this
group regarding other Hyalinobatrachium. We agree
with this hypothesis and consider that H. iaspidiense
and H. mesai form a monophyletic group supported by
the synapomorphy of blotches of iridophores on the
dorsal parietal peritoneum.
Figure 2. Hyalinobatrachium iaspidiense (MZUNAP 0517)
from Lago Preto-Paredón, department of Loreto, Republic of
Peru.
Figure 3. Map of northern South America showing the known localities of Hyalinobatrachium iaspidiense based on the new
localities reported herein (closed symbols) and literature records (open symbols): (1) Quebrada Jaspe, (2) Caño Colima, (3)
mountain areas of Kaw, Monts Trinité, Courcibo, and Saut Arataye/Nouragues Reserve, (4) President Figueiredo, (5) lower River
Cristalino region, (6) Mabura Hill Forest Reserve, (7) Sipaliwini district, (8) Cofán-Dureno territory, (9) Lago Preto-Paredón.
Country codes: Venezuela = Ve; Colombia = Co; Ecuador = Ec; Peru = Pe; Guyana = Gu; Suriname = Su; French Guiana = FG;
Brazil = Br; Bolivia = Bo.
Acknowledgments. We are grateful to Roy W. McDiarmid,
Janalee Caldwell, Gilson Rivas, and Santiago Castroviejo-Fisher
for their helpful comments and discussions. We thank Pablo
Puertas, Richard Bodmer, Angel Chimbo, Corine Vriesendorp,
Sebastian Descanse, and Alvaro del Campo for eld and
laboratory assistance, Mark Bowler for taking the pictures;
and María Olga Borja for pre-reviewing the manuscript. M.
Yánez-Muñoz’s research was supported by the Field Museum
of Chicago through their Rapid Biological Inventories,
Environmental and Conservation Program coordinated by Corine
Vriesendorp, Debora Moskovits, and Randall Borman. P. Pérez-
Peña’s research was supported by Wildlife Conservation Society–
Peru. D. Cisneros-Heredia’s research was supported by Ma. E.
Heredia and L. Heredia, the Smithsonian Women’s Committee,
the 2002 Research Training Program at the National Museum
of Natural History-Smithsonian Institution, King’s College
London, Universidad San Francisco de Quito, the Russel E. Train
Education for Nature Program of the Word Wildlife Fund WWF,
and the ‘‘Fernando Ortíz-Crespo’’ Endangered Species Program
managed by EcoCiencia and Conservation International.
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Mario Yánez-Muñoz et al.
52
Accepted by Sebastian Steinfartz
... Hyalinobatrachium iaspidiense is a poorly known glassfrog species that was originally described from the Venezuelan Guiana Shield (Ayarzagüena, 1992). Additional reports of this species include other localities in the Guianas (e.g., Kok and Castroviejo-Fisher, 2008 for the junior synonym H. nouraguense Lescure & Marty, 2000;Castroviejo-Fisher et al., 2011;Ouboter and Jairam, 2012;Cole et al., 2013) and major parts of the Amazon Basin in Brazil, Ecuador, and Peru (e.g., Guayasamin and North, 2009;Yánez-Muñoz et al., 2009). Herein, we report H. iaspidiense from two new localities, one from the upper Amazon Basin in Pastaza Province, Ecuador, and the other from Loreto Department, Peru. ...
... To the best of our knowledge, H. iaspidiense is now known from five localities in Ecuador, including in Napo, Orellana, Pastaza, and Sucumbíos provinces ( Fig. 3; Guayasamin and North, 2009;Yánez-Muñoz et al., 2009;Guayasamin et al., 2020; this study). The new record extends the species' range 43 km southwestwards, reaching into the Andean foothills. ...
... With an elevation of 950 m, this specimen corroborates the species' upper elevational limit, stated to be 800-1000 m (Ayarzagüena, 1992;Castroviejo-Fisher et al., 2011). The locality is situated substantially higher than the other Ecuadorian localities, which range from 280-405 m (Guayasamin and North, 2009;Yánez-Muñoz et al., 2009;Guayasamin et al., 2020). Hyalinobatrachium iaspidiense occurs at this locality in syntopy with at least two other centrolenid species, Teratohyla midas (Lynch & Duellman, 1973), and Chimerella mariaelenae (Cisneros-Heredia & McDiarmid, 2006), which were all found together along the same stream. ...
Article
Full-text available
We have added two new records (in Ecuador and Peru) and maximun altitude of the glass frog "Hyalinobatrachium iaspidiense"
... The only species with a similar dorsal coloration is H. mesai, a species known only from the southern slope of Sarisariñama-tepui, Venezuela [224]. It has been suggested, however, that H. mesai and H. iaspidiense represent the same species [223]. Diagnosis: (1) Vomerine teeth absent; (2) snout truncated in dorsal aspect and slightly protruding in profile; (3) tympanum not visible; supratympanic fold absent; (4) dorsal skin shagreen; (5) venter smooth; pair of enlarged subcloacal warts, but low and difficult to see; (6) ventral parietal peritoneum transparent (condition P0); pericardium transparent; white peritoneum covering intestines and stomach; transparent peritoneum on urinary bladder (condition V6); (7) liver bulbous, hepatic peritoneum white (condition H2); (8) humeral spines absent; (9) webbing absent between Fingers I, II, and III, moderate between outer fingers; webbing formula III (2-2 + ) -(1 + -2 − ) IV; (10) webbing between toes moderate; webbing formula on foot I (1-1 + ) -(2 + -2 1/3 ) II (1 + -1 1/3 ) -(2 + -2 1/4 ) III (1-1 + ) -(2-2 3/4 ) IV (2 + -2 1/4 ) -(1 + -1 1/4 ) V; (11) ulnar fold present, enameled; external tarsal fold present, enameled; internal tarsal fold short and low; (12) concealed prepollex; nuptial pad Type IV; (13) Finger II shorter than Finger I (Finger II about 93% of Finger I); (14) disc of Finger III width 39%-57% of eye diameter; (15) Color in life ( Figure 112): Dorsum translucent, with a yellowish-green background coloration, large lime-green blotches, and small black spots. ...
... Diagnosis: (1) Vomerine teeth absent; (2) snout truncated in dorsal aspect and slightly protruding in profile; (3) tympanum not visible; supratympanic fold absent; (4) dorsal skin shagreen; (5) venter smooth; pair of enlarged subcloacal warts, but low and difficult to see; (6) ventral parietal peritoneum transparent (condition P0); pericardium transparent; white peritoneum covering intestines and stomach; transparent peritoneum on urinary bladder (condition V6); (7) liver bulbous, hepatic peritoneum white (condition H2); (8) humeral spines absent; (9) webbing absent between Fingers I, II, and III, moderate between outer fingers; webbing formula III (2-2 + ) -(1 + -2 − ) IV; (10) webbing between toes moderate; webbing formula on foot I (1-1 + ) -(2 + -2 1/3 ) II (1 + -1 1/3 ) -(2 + -2 1/4 ) III (1-1 + ) -(2-2 3/4 ) IV (2 + -2 1/4 ) -(1 + -1 1/4 ) V; (11) ulnar fold present, enameled; external tarsal fold present, enameled; internal tarsal fold short and low; (12) concealed prepollex; nuptial pad Type IV; (13) Finger II shorter than Finger I (Finger II about 93% of Finger I); (14) disc of Finger III width 39%-57% of eye diameter; (15) Color in life ( Figure 112): Dorsum translucent, with a yellowish-green background coloration, large lime-green blotches, and small black spots. Venter transparent, pericardium transparent (red heart visible), visceral and hepatic peritonea white [223,225]. ...
... Type locality: "Saut Arataye (environs du camp de base), Réserve des Nouragues (bassin de l'Approuague), Guyane française". Placed in synonymy by Yánez-Muñoz, Pérez-Peña, and Cisneros-Heredia, 2009[223]. ...
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Glassfrogs (family: Centrolenidae) represent a fantastic radiation (~150 described species) of Neotropical anurans that originated in South America and dispersed into Central America. In this study, we review the systematics of Ecuadorian glassfrogs, providing species accounts of all 60 species, including three new species described herein. For all Ecuadorian species, we provide new information on the evolution, morphology, biology, conservation, and distribution. We present a new molecular phylogeny for Centrolenidae and address cryptic diversity within the family. We employ a candidate species system and designate 24 putative new species that require further study to determine their species status. We find that, in some cases, currently recognized species lack justification; specifically, we place Centrolene gemmata and Centrolene scirtetes under the synonymy of Centrolene lynchi; C. guanacarum and C. bacata under the synonymy of Centrolene sanchezi; Cochranella phryxa under the synonymy of Cochranella resplendens; and Hyalinobatrachium ruedai under the synonymy of Hyalinobatrachium munozorum. We also find that diversification patterns are mostly congruent with allopatric speciation, facilitated by barriers to gene flow (e.g., valleys, mountains, linearity of the Andes), and that niche conservatism is a dominant feature in the family. Conservation threats are diverse, but habitat destruction and climate change are of particular concern. The most imperiled glassfrogs in Ecuador are Centrolene buckleyi, C. charapita, C. geckoidea, C. medemi, C. pipilata, Cochranella mache, Nymphargus balionotus, N. manduriacu, N. megacheirus, and N. sucre, all of which are considered Critically Endangered. Lastly, we identify priority areas for glassfrog conservation in Ecuador.
... Males of this species lack humeral spines (Guayasamin and North 2009; Castroviejo-Fisher et al. 2011). Hyalinobatrachium iaspidiense is known from Brazil (Yáñez-Muñoz et al. 2009; Ávila-Pires et al. 2010; Castroviejo-Fisher et al. 2011 ), Ecuador (Muñoz et al. 2009; Guayasamin and North 2009), French Guiana (Lescure and Marty 2000; Castroviejo-Fisher et al. 2011), Guyana (Ernst et al. 2005; Cole et al. 2013), Peru Check List 12(2): 1849, 2 March 2016 doi: http://dx.doi.org/10.15560/12.2.1849 ISSN 1809-127X © 2016 Check List and Authors Brazil. ...
... Males of this species lack humeral spines (Guayasamin and North 2009; Castroviejo-Fisher et al. 2011). Hyalinobatrachium iaspidiense is known from Brazil (Yáñez-Muñoz et al. 2009; Ávila-Pires et al. 2010; Castroviejo-Fisher et al. 2011 ), Ecuador (Muñoz et al. 2009; Guayasamin and North 2009), French Guiana (Lescure and Marty 2000; Castroviejo-Fisher et al. 2011), Guyana (Ernst et al. 2005; Cole et al. 2013), Peru Check List 12(2): 1849, 2 March 2016 doi: http://dx.doi.org/10.15560/12.2.1849 ISSN 1809-127X © 2016 Check List and Authors Brazil. ...
... Silva e Silva and Costa-Campos | First record of Hyalinobatrachium iaspidiense for the state of Amapá (Yáñez-Muñoz et al. 2009; Castroviejo-Fisher et al. 2011Castroviejo-Fisher et al. 2011). Here we report a new record of Hyalinobatrachium iaspidiense in the municipality of Serra do Navio (00°54ʹ50ʺ N, 051°59ʹ59.2ʺ ...
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We report the first record of Hyalinobatrachium iaspidiense (Ayarzaguena, 1992) from Amapá state, Brazil. This record is 1,020 km east from the type locality at Quebrada de Jaspe, San Ignacio de Yuraní, Bolívar state, Venezuela, and extends the distribution of the species 345 km north of the nearest known locality in Para. We also provide a map of the localities reported in the literature.
... Desde el año 2004 se han publicado cerca de cuatro artículos por año relacionados con la diversidad de ranas de cristal (Centrolenidae) del Ecuador [1, 2, 3, 4, 5, 6,7,8,9,10,11,12,13,14,15,16,17,18,19,20,21,22,23,24,25]. Gran parte del incremento al conocimiento de este grupo se debe al proyecto "Ranas de Cristal" mentalizado y dirigido por Diego F. Cisneros-Heredia (entrar a centrolenidae.cisneros-heredia.org, ...
... Los ecosistemas de bosques de Neblina y Montanos en los sectores de las cuencas del Pastaza y Santiago no han sido bien estudiados; por ejemplo, mientras que al norte en la cuenca del Napo se han registrado hasta siete especies en bosques nublados; hacia el centro y sur solo se han reportado tres especies en ese ecosistema. Los métodos tradicionales para muestreos de anfibios (e.g., relevamientos de encuentros visuales) parecen no ser efectivos para registrar ranas centrolénidas; por ejemplo, a pesar de las prolijas colectas realizadas por Duellman [35] en la cuenca del Aguarico durante 6 años, nunca obtuvo registros de Hyalinobatrachium iaspiedensi o Nymphargus puyoensis, especies que si están presentes en esa zona [25]. Es trascendental juntar todos los esfuerzos posibles para investigar y conservar este grupo de la fauna ecuatoriana, en especial cuando las políticas gubernamentales apuestan por el extractivismo minero y una avalancha de proyectos hidroeléctricos en la región que afectarían a la supervivencia a largo plazo de la biodiversidad del oriente Ecuatoriano. ...
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Presentamos nueva información que extiende la distribución latitudinal y altitudinal de cinco especies de ranas de cristal recientemente descritas y poco conocidas de la región oriental de Ecuador. Incluimos datos novedosos sobre su tamaño corporal e historia natural. Se discute información sobre la diversidad y biogeografía de ranas centrolenidas del oriente de Ecuador, encontrando que se encuentran asociadas con seis formaciones vegetales comprendidas entre las estribaciones orientales y la baja Amazonia. Identificamos tres importantes zonas de diversidad y endemismo en la región oriental de Ecuador asociadas con las cuencas hidrográficas de los ríos Napo, Pastaza y Santiago. Los ecosistemas de bosques Montano Bajos y Piemontanos concentran la mayor diversidad y endemismo para ranas centrolenidas, sin embargo 77% de ellas están amenazadas. Es trascendental juntar todos los esfuerzos posibles para investigar y conservar este substancial grupo de la fauna ecuatoriana.
... Distribution: Region 5. Considered until recently endemic to the Venezuelan Gran Sabana. For several years, reports of this species have come from French Guiana, Surinam, Brazil, Ecuador, and Peru (Guayasamin and North 2009;Yánez-Muñoz et al. 2009), showing one of the widest distributions among centrolenid frogs. In Venezuela, however, only known from the southeastern sector (east of the Parima-Maigualida mountain chain). ...
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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. Eleutherodactylus terraebolivaris Rivero, 1961 is synonymized with Hylodes incertus Lutz, 1927 as Pristimantis incertus. Oreophrynella dendronastes Lathrop and MacCulloch, 2007, is considered a junior synonym of O. macconnelli (Boulenger 1895). Centrolene Jiménez de la Espada, 1872, is a feminine genus, so all species in the genus are amended. Centrolenella pulidoi Rivero, 1968 is considered a junior synonym of Hyla benitezi Rivero, 1961, as Boana benitezi. Centrolenella estevesi Rivero, 1968 is considered a junior synonym of Hyla jahni Rivero, 1961, as Hyloscirtus jahni. Illustrated herein are 300 species (77.5% of the total). Lastly, the distributions for all species are revised, species that possibly occur within Venezuela are suggested, and comments are provided on nomenclature and conservation issues. Resumen.—Se presenta una lista anotada de los anfibios de Venezuela, actualizada hasta diciembre de 2018. La última lista comprensiva (Barrio-Amorós 2019c) incluyó un total de 333 especies, mientras que la lista actual contiene 387 especies (370 anuros, 10 cecilias y siete salamandras), incluyendo 28 especies aun no descritas o identificadas propiamente. 50 especies y cuatro géneros se añaden a la lista previa, 25 especies se eliminan y 47 de ellas han experimentado cambios nomenclaturales. Eleutherodactylus terraebolivaris Rivero, 1961 se sinonimiza con Hylodes incertus Lutz, 1927, como Pristimantis incertus. Oreophrynella dendronastes Lathrop and MacCulloch, 2007, se considera sinónimo de O. macconnelli (Boulenger, 1895). Centrolene Jiménez de la Espada, 1872, es un género femenino, así que se emendan todos los nombres acorde. Centrolenella pulidoi Rivero, 1968 es considerado sinónimo de Hyla benitezi Rivero, 1961, como Boana benitezi. Centrolenella estevesi Rivero, 1968, se considera sinónimo de Hyla jahni Rivero, 1961, como Hyloscirtus jahni. Se presentan fotografías de 300 especies (77.5% del total). Por último, la distribución de todas las especies es revisada, se sugieren especies que podrían estar presentes en Venezuela y se presentan comentarios sobre nomenclatura y conservación.
... The diversity of species of frogs of the family Centrolenidae is highest in Colombia and Ecuador, diminishing northward and southward. The number of species in Ecuador has increased significantly since Lynch & Duellman (1973) and Duellman & Burrowes (1989), with 10 species described as new since 2004; and currently 32% (48 spp.) of the known anuran species of the family Centrolenidae (glassfrogs) have been reported to inhabit in the Republic of Ecuador (see subsequent publications: Cisneros-Heredia et al., 2008;Cisneros-Heredia & Morales-Mite, 2008;Guayasamin et al., 2008a;Yánez-Muñoz & Cisneros-Heredia, 2008;Yánez-Muñoz et al. 2009). Knowledge about the glassfrogs from Ecuador is still fragmented and its species richness is expected to increase with the study of unidentified museum specimens and the discovery of additional species with the exploration of previously uncollected areas (Cisneros-Heredia & McDiarmid 2006a, b, 2007. ...
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FIGURE 3. (A): Teratohyla amelie; (B): Teratohyla midas; (C): Teratohyla pulverata; (D): Teratohyla spinosa; (E): Teratohyla sornozai sp. nov. Photos by P. Meza-Ramos, A. Georges, M. H. Yánez-Muñoz, R. W. McDiarmid, and H. M. Ortega-Andrade, respectively.
... described Rulyrana mcdiarmidi from Ecuador and Peru, and presented the first record of Nymphargus posadae from Peru. Muñoz et al. (2009) reported the first Peruvian record of Hyalinobatrachium iaspidiense Ayarzagüena from Amazonian Peru. Castroviejo-Fisher et al. (2009) described Hyalinobatrachium carlesvilai Castroviejo-Fisher, Padial, Chaparro, Aguayo & de la Riva from the Amazonian slopes of central Andean Peru, assigned all previous records of H. munozorum from Peru either to H. carlesvilai or to H. bergeri, synonymized H. lemur with H. pellucidum Lynch & Duellman, and extended the distribution of the latter south to the department of Cusco, southern Peru. ...
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