ISSN 1827-9635 (print) © Firenze University Press ISSN 1827-9643 (online) www.fupress.com/ah Acta Herpetologica 7(2): 341-345, 2012 Range extension of the critically endangered true poison-dart frog, Phyllobates terribilis (Anura: Dendrobatidae), in western Colombia Roberto Márquez1,*, Germán Corredor2, Carlos Galvis3 Daniel Góez2, Adolfo Amézquita1 1 Department of Biological Sciences, Universidad de los Andes, AA 4976. Bogotá D.C., Colombia. *Cor- responding author. E-mail: roberto.marquez33@gmail.com 2 Biology Department, Universidad del Valle, AA 25360, Cali, Colombia 3 Cali Zoological Foundation, Carrera 2 oeste Calle 14 esquina, Barrio Santa Teresita. Cali, Colombia Submitted on: 2012, 26th September; revised on: 2012, 22nd October; accepted on: 2012, 24th October. Abstract. The poison-dart frog Phyllobates terribilis is currently classified as endan- gered or critically endangered due to its extremely restricted geographic distribution and intensive smuggling by pet traffickers. Based on molecular data, we here report two new localities representing a 60 km northward extension of its previously recog- nized range. The identity of other Phyllobates populations in western Colombia is dis- cussed, as well as the current morphological criteria used to distinguish P. terribilis and the similar P. bicolor. Keywords. Phyllobates terribilis, geographic distribution, DNA barcoding, conserva- tion status. The Golden Poison-Dart Frog, Phyllobates terribilis, is one of the three species that was used by the Emberá people of western Colombia to poison darts, and is by far the most toxic among them. The species was described by Myers et al. (1978), based on speci- mens collected at Quebrada Guangüí (type locality) and La Brea, about 8 km west of the type locality, in the Departamento del Cauca, Colombia, which remained the only known localities for almost 20 years. While topotypic specimens are yellow to orange, a mint- colored morph was later reported from La Sirpa near the mouth of the Saijá River, about 15 km west of Quebrada Guangüí (Lötters et al., 1997). In the same paper, two series of Phyllobates frogs collected about 50 km south of Buenaventura (Departamento del Valle del Cauca), and 70 km north of the type locality, were reported to exist at the herpetologi- cal collection of the Universidad del Valle, Cali (UVC 7208-7210, 7135-7137). These were tentatively diagnosed as Phyllobates bicolor, based on their snout-vent length (SVL) and their blackish distal limb and throat coloration. Moreover, it was suggested that P. terribilis 342 Roberto Márquez et al. could represent an extreme of clinal variation in P. bicolor (Lötters et al., 1997). Recent molecular analyses have, however, unambiguously supported P. bicolor and P. terribilis as two separate and well differentiated species (Grant et al., 2006). Because it was unclear whether specimens of Phyllobates occurring south of Bue- naventura, belonged to either P. bicolor, or P. terribilis, we used DNA barcoding to diag- nose frogs from two localities in southern Departamento del Valle del Cauca: (1) Río Naya (3°17’N, 77°24’W) and (2) Boca Yurumanguí (3°23’N, 77°18’W), in the Naya and Yurumanguí river drainages, respectively (Fig. 1). We refrain from providing more detailed coordinates due to the intensive smuggling suffered by this frog species and its very restricted distribution range, which led Castro (2004) to declare P. terribilis as one of the few critically endangered amphibian species in Colombia. We captured four individuals at Río Naya and two at Boca Yurumanguí. We measured their SVL and collected tissue samples by mouth-swabbing. Two frogs from each local- ity were maintained as vouchers (field numbers GECOH 355, GECOH 434, GECOH 643, and GECOH 1163; Fig. 2) and the other ones released. Specimens from Río Naya ranged 38-41 mm (mean 39.75, standard deviation 1.22) and those from Yurumanguí were 37 and 40 mm in SVL. DNA was extracted from the collected epithelial tissue using DNeasy Animal Blood and Tissue Kits (Qiagen), and the 5’ fragment of the Cytochrome c oxidase I (COI) mito- Fig. 1. Reported localities of Phyllobates terribilis, including those reported in this paper. 343Distribution of Phyllobates terribilis chondrial gene was sequenced by using the dgLCO1490 and dgHCO2198 primers (Meyer et al., 2005). The obtained sequences were deposited in GenBank under accession num- bers JX887784-JX887787. We then used the Barcode of Life Database Identification Sys- tem (BOLD IDS; http://www.boldsystems.org/) to identify the sequences that best matched the query sequences from our specimens. To further corroborate our results, we inferred Bayesian and maximum likelihood gene trees using MrBayes (Ronquist and Huelsen- beck, 2003) and RAxML (Stamatakis, 2006), respectively, from our sequences and all CO1 sequences from Phyllobates species available in GenBank (Fig. 3; Grant et al., 2006). The two sequences from Río Naya were 99.8% similar among them, and those from Boca Yurumanguí were identical. The BOLD IDS yielded a 0.992 probability of assign- ing the two Boca Yurumanguí sequences to P. terribilis, and 0.987–0.988 probabilities of assigning the Río Naya individuals to the same species, which was the best match for the four sequences. Assignment probabilities to P. bicolor (0.940, 0.935–0.936, respectively) were lower in all cases. Regarding the gene tree, the four query sequences were nested within a very well supported clade that included all the other P. terribilis sequences (Fig. 3). Hence, both the barcoding and phylogenetic analyses strongly support the frogs from Boca Yurumanguí and Río Naya as part of P. terribilis. Given the short geographic distance (Fig. 1) between the localities reported here and the other two localities referred to by Lötters et al. (1997) and the similar body size (all the collected adults range from 38.2–41.2 mm) among all these frogs, as well as their Fig. 2. Ventral and dorsal views of P. terribilis from A-B. Río Naya and C-D. Boca Yurumanguí. 344 Roberto Márquez et al. blackish distal limb and throat coloration, it is most likely that frogs referred by them (including those tentatively assigned to P. bicolor) are indeed P. terribilis. Myers et al. (1978) suggested that the only useful morphological characters at distin- guishing bicolor and terribilis were color pattern and body size. Our data suggest other- wise, posing a potential conflict between genetic and morphologic (traditionally based on body size and color) diagnosis of both species. Further taxonomic and phylogenetic stud- ies with much wider sampling are urgently needed to clarify this issue. Our results expand the distribution of P. terribilis about 60 km north of its previously known range, with the proposed distribution now including localities in two departments of western Colombia (Cauca and Valle del Cauca). Since one of the motives leading to the classification of P. terribilis as critically endangered (Rueda-Almonacid et al., 2004) or endangered (Bolivar and Lötters, 2004) was its very restricted extension of range, our findings could improve the conservation status of the species. However, further field cen- suses and studies are necessary to conduct a thorough reevaluation of the conservation status of P. terribilis. Fig. 3. Bayesian gene tree inferred from CO1 sequences of Phyllobates spp. available in GenBank and those of frogs collected in two new localities (in bold). The numbers on internodes represent Bayesian posterior probabilities followed by ML bootstrap values (1000 pseudoreplicates). 345Distribution of Phyllobates terribilis ACKNOWLEDGEMENTS The authors would like to thank the Epeara Siapidara indigenous community for their sup- port and hospitality, as well as the Fundación Zoológica de Cali and the Faculty of Sciences at Uni- versidad de los Andes for providing financial support. RM and AA were supported by a Colombia Biodiversa Scolarship from the Alejandro Ángel Escobar Foundation. We would also like to thank an anonymous reviewer and Ylenia Chiari whose comments improved the quality of the manuscript. REFERENCES Bolívar, W., Lötters, S. (2004): Phyllobates terribilis. In: IUCN Red List of Threatened Spe- cies. Version 2012.1. http://www.iucnredlist.org/details/biblio/55264/0. Sept. 15 2012. Castro, F. (2004): Rana venenosa dorada - Phyllobates terribilis. In: Libro rojo de los anfibi- os de Colombia, pp. 178–182. Rueda-Almonacid, J. V., Lynch, J. D., Amézquita, A., Eds, Conservación Internacional Colombia, Instituto de Ciencias Naturales, Univer- sidad Nacional de Colombia, Ministerio del Medio Ambiente. Bogotá, Colombia. Grant, T., Frost, D.R., Caldwell, J.P., Gagliardo, R., Haddad, C.F.B., Kok, P.J.R., Means, D.B., Noonan, B.P., Schargel, W.E., Wheeler, W.C. (2006): Phylogenetic systematics of dart-poison frogs and their relatives (Amphibia: Athesphatanura: Dendrobatidae). Bull. Amer. Mus. Nat. Hist. 299: 1-262. Lötters, S., Castro, F., Köhler, J., Richter, R. (1997): Notes on the distribution and color variation of poison frogs of the genus Phyllobates from western Colombia (Anura: Dendrobatidae). Rev. Fr. Aquariol. 24: 55-58. Meyer, C.P., Geller, J.B., Paulay, G. (2005): Fine scale endemism on coral reefs: archipe- lagic differentiation in turbinid gastropods. Evolution 59: 113-125. Myers, C.W., Daly, J., Malkin, B. (1978): A dangerously toxic new frog (Phyllobates) used by Emberá Indians of western Colombia, with discussion of blowgun fabrication and dart poisoning. Bull. Amer. Mus. Nat. Hist. 161: 311-366. Ronquist, F., Huelsenbeck, J.P. (2003): MrBayes 3: Bayesian phylogenetic inference under mixed models. Bioinformatics 19: 1572-1574. Stamatakis, A. (2006): RAxML-VI-HPC: maximum likelihood-based phylogenetic analy- ses with thousands of taxa and mixed models. Bioinformatics 22: 2688-2690. Acta Herpetologica Vol. 7, n. 2 - December 2012 Firenze University Press Advertisement call of species of the genus Frostius Cannatella 1986 (Anura: Bufonidae) Flora A. Juncá1, David L. Röhr2, Ricardo Lourenço-de-Moraes3, Flávio J. M. Santos1, Airan S. Protázio1, Ednei A. 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