Atelopus zeteki
Panamanian Golden Frog
family: Bufonidae

© 2013 John P. Clare (1 of 59)

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Conservation Status (definitions)
IUCN (Red List) Status Critically Endangered (CR)
CITES Appendix I
Other International Status None
National Status None
Regional Status None


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Atelopus zeteki, the Panamanian golden frog, is a small, brightly-colored frog. Adult dry forest males measure 35-40 mm in SVL and weigh 3-5 g; adult dry forest females measure 45-55 mm and weigh 4-7 g. Wet forest males and females are larger; adult males measure 39-48 mm in SVL and weigh 8-12 g, while adult females measure 55-63 mm and weigh 10-15 g (Poole 2006). The head is longer than broad, with a pointed, protuberant snout and rounded canthus rostralis (Savage 2002). The pupil is horizontally elliptical (Savage 1972). There is no tympanum, and the ostia pharyngea are slitlike or absent, implying the lack of other middle ear structures such as the auditory ossicle and middle ear cavity (in common with most other species of Atelopus) (Lindquist and Hetherington 1996). However, standard inner ears with well-developed auditory end organs are present (Savage 2002; Lindquist and Hetherington 1996). The body is slim with long limbs, and the upper surface is smooth with minute spicules; when magnified, the skin takes on a shagreened appearance (Savage 2002; Savage 1972). The fingers are elongate and narrow. The first finger is much shorter than the second, and there is basal webbing between the first and second fingers in atelopid males; the other fingers are free. The undersides of the hands are wrinkled and fleshy, having only a large rounded thenar tubercle but no other tubercles. The toes are extensively webbed with only toe IV substantially free of webbing, and the undersides of the feet are fleshy and wrinkled with smooth subarticular tubercles. No tarsal fold is present, and the inner and outer metatarsal tubercles are moderate, smooth, and rounded, with the inner metatarsal tubercle being larger. Paired elongate vocal slits are present along with a single internal vocal sac in adult atelopid males. Males also have a well-developed brownish nuptial pad on the upper and inner surface of the first finger (Savage 1972).

The sexes have similar coloration, and the coloration is usually uniform golden yellow with one to several large black dorsal markings (Savage 1972). Normally the abdomen is also yellow, but when carrying eggs, the female's ventral surface will have a lighter-colored abdomen (Poole 2006).

At stage 36, the tadpole body length is 5.8 mm, with a body width of 4.3 mm, and total length of 12.2 mm. The larval body is ovoid, with the greatest width at the body midpoint. The body is also depressed, and flattened ventrally, being about 3/5 as high as wide. Nares (nostrils) are small and located closer to the eyes than the tip of the snout. Eyes are dorsal and directed anterodorsolaterally; they are moderately large, nonbulging, and separated by a distance 1.5 times the diameter of the eye. Atelopus zeteki tadpoles are gastromyzophorous, possessing a large sucker that covers the anterior part of the belly and numerous tooth rows. The tadpole mouth is large, ventral, and surrounded by labia forming an unbroken oral disc 3.6 mm wide. The posterior lip has no papillae, while other lips bear a single row of small blunt papillae. The rows are complete and roughly equal in length. Beaks are thin and smooth. A large ventral suctorial disc extends and broadens from the posterior labium. The suctorial disc lacks papillae. On the venter, the spiracle is sinistral, medial, elongate, and directed posteriorly. The vent tube is moderate in length and medial. Caudal musculature is well defined and deep on the anterior half of the tail, narrowing abruptly at midlength and extending nearly to the tip. The tip of the tail is moderately rounded (Lindquist and Hetherington 1998b).

Tadpoles (at least in captivity) are completely white for the first few days post-hatching, developing pigmentation after a few days (Poole 2006). At that point the larval coloration begins to change to dark brown to black dorsally with metallic gold flecks. The venter is pale gray to translucent. Metamorphosing tadpoles (stage 45) have lost the gold flecking and gained small dark green markings against the dark brown dorsum, and are slightly darker than fully metamorphic juveniles (Lindquist and Hetherington 1998b).

Newly metamorphosed froglet size is 6 mm in SVL, in captive-bred frogs (Poole 2006). Recent metamorphs are vivid green with dark black or brown markings, matching the color of mosses growing on stones in or around the stream habitat (Lindquist and Hetherington 1998b). Dorsal markings on the metamorphs always include the following: brick-red warts inside the dorsal markings; a rostral spot or band running transversely, an interorbital "X" from the crest of the eyes to the suprascapular area, a single lumbar chevron with the point towards the anterior of the frog and ending at the flanks, a transverse post-sacral band, and 1-3 lateral bands encircling arms and legs. In addition,the digits sometimes have markings. Palmar and plantar surfaces are also yellow (Lindquist and Hetherington 1998b). The juvenile venter may be either yellow or white, without markings or spotted. If the venter is white, there is a yellow anal patch. Juveniles from El Cope, Panama, had differences in ventral coloration (yellow or white), and it is not known whether this might be sexually dimorphic. In contrast, juveniles at Campana Heights, Panama, had only yellow venters, but were also thought to be older than those observed at El Cope (Lindquist and Hetherington 1998). It is not until the frogs reach older juvenile to subadult age that they undergo ontogenetic color change and acquire the typical yellow or goldenrod overall ground color. In addition, adults that have black patterning have considerably narrower markings than do metamorphic or subadult frogs (Lindquist and Hetherington 1998b), implying that the extent of black marking also changes with age.

Distribution and Habitat

Country distribution from AmphibiaWeb's database: Panama


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Atelopus zeteki occurs in western-central Panama, in the Central Cordilleran rainforests and cloudforests (Lindquist and Hetherington 1998b), from 335-1,315 m above sea level (Stuart et al. 2008). They are found associated with montane streams in two habitat types, montane wet forest and montane dry forest. (Poole 2006).

Life History, Abundance, Activity, and Special Behaviors
Panamanian golden frogs are terrestrial, diurnal forest frogs that generally occur near rapid-flowing small streams (Savage 1972). Occasionally males are heard calling in the forest far from the water, more than 50 m away (Lindquist and Hetherington 1998b). These frogs move by a distinctive ambling walk (Savage 1972), and consume a variety of small invertebrates (Savage 2002). Panamanian golden frogs protect themselves from predators by skin secretions of a unique and potent nerve-poison called zetekitoxin (see Comments section below) (Savage 2002).

In wet forest stream habitats, the frogs are dispersed in and along streams. They can climb and are found up to 3 meters above ground, perching on large moss-covered boulders near waterfalls and along the banks of streams. In contrast, in dry forest stream habitats the frogs are smaller (2/3 the size), distributed mainly over the forest floor, and occur only up to 1.5 meters above ground. The population density of Panamanian Golden Frogs is higher in dry forests than in wet forests (Poole 2006).

Female frogs move into the forests in the late dry and early rainy season (February-March) and return to streams to breed in the late rainy and early dry season (November-January) (Karraker et al. 2006). Males tend to stay in streams year-round establishing territories and waiting for the females to return (Poole 2006). Male frogs perch on rocks in or along the banks of streams and waterfalls, and they defend their territory by semaphoring (hand-waving, plus an unusual form of foot-raising--not foot-flagging, and reorientation) (Lindquist and Hetherington 1996; Lindquist and Hetherington 1998a; Lindquist and Hetherington 1998b). Males also vocalize, but prefer semaphoring over vocalization, apparently due to the noisiness of waterfalls and stream flow in their natural habitat (Lindquist and Hetherington 1996). Females also semaphore in this species, as they do in the related species Atelopus varius (Lindquist and Hetherington 1998a; Crump 1988). There is a male-favored gender bias, resulting in the majority of males being single, and thus all females encountered in streams are amplexed (Poole 2006). Amplexus can last from a few days to two months in captivity (Poole 2006).

Oviposition occurs in wider stream sections along shallow margins, where the water runs quickly and there is slightly lower canopy closure, during periods of lower water flow (Karraker et al. 2006). The mean depth of preferred streams in Karraker et al.'s (2006) study was 16.5 � 15.7 cm, and the mean stream velocity was 0.34 � 0.15 m/s, with a mean water temperature of 23.4�C � 0.8�C. A single string of cream-colored eggs is attached to a rocky stream substrate, which is most often large (such as a boulder or bedrock) (Karraker et al. 2006). Selection of larger substrates in confined channels may reduce the risk of eggs being washed downstream in late rainy season storms (Karraker et al. 2006). The single strand is looped back upon itself, forming two or more layers of eggs in a loose, elongated mass (Karraker et al. 2006). Average clutch size is 370 eggs (ranging from 202-623), with an average ovum diameter of 1.8 mm (Karraker et al. 2006). Clutches are usually found within 2 m of the stream border and are evenly distributed between riffle and run habitats; they are generally placed 1.1 � 1.3 m apart, implying communal oviposition (Karraker et al. 2006). It has been suggested that if this is communal oviposition, it may occur in Atelopus zeteki in order to distribute the risk of predation and to accommodate a lack of suitable oviposition sites (Karraker et al. 2006). In captivity, the embryonic development ranged from 7-11 days at 22.0�C and averaged 8.9 � 1.3 days (Detroit Zoo unpublished cited in Karraker et al. 2006).

Tadpoles are commonly found resting on top of stones and stream gravel at the edges of shallow pools below cascades (Lindquist and Hetherington 1998). Their coloration is similar to the color of the sand, which is the predominant surrounding substrate (Karraker et al. 2006). They may live anywhere along the stream where water pools, as long as the pool is directly connected to flowing channels. They prefer water depths of 5-35 cm (Lindquist and Hetherington 1998b). The development of the larvae takes place with the onset of the wet season, and the possession of a large ventral adhesive disk allows the larvae to remain attached to objects on the bottom of the stream against the torrential current (Savage 1972). However, Karraker et al. (2006) observed that the ventral suctatorial disc of newly hatched Atelopus zeteki larvae is either undeveloped or not yet functional immediately upon hatching. It is not known at what point the disc acquires functionality.

Juveniles were always observed within 2 m of the stream (Lindquist and Hetherington 1998b). Interestingly, although adult males are territorial and do not allow conspecifics other than gravid females to approach, Lindquist and Hetherington (1998b) observed subadults in close proximity and sometimes even touching adult males. However, as soon as significant rainfall began, all juveniles vanished from open streamside areas used by adult males. Lindquist and Hetherington (1998b) hypothesized this might be due to rain triggering territorial defense behavior in adult A. zeteki males.

Trends and Threats
This species has declined in numbers by over 80% over the past decade, most likely due to chytridiomycosis (Stuart et al. 2008). It is also threatened by collection for local zoos and hotels, illegal pet trading, deforestation, and habitat alteration by logging and farming (Poole 2006). Project Golden Frog is an ongoing conservation consortium which connects the Republic of Panama and the United States, in an effort to ensure the survival of this species. Plans for captive breeding in Panama are being supported by Project Golden Frog. Captive breeding programs for this species are already in place at a number of zoos, including the Maryland Zoo in Baltimore, the Houston Zoo, the Denver Zoo, the Detroit Zoo, and the Oakland Zoo.

Relation to Humans
Atelopus zeteki is the Panamanian national animal. As a cultural symbol, it represents good fortune and is frequently shown on lottery tickets. Panamanian golden frogs are often captured and used to promote hotels, restaurants, and tourism. They were revered by Pre-Columbian indigenous people and images of this frog were crafted in gold and clay talismans called huacas (Poole 2006).

Possible reasons for amphibian decline

General habitat alteration and loss
Habitat modification from deforestation, or logging related activities
Local pesticides, fertilizers, and pollutants
Intentional mortality (over-harvesting, pet trade or collecting)

Atelopus zeteki is the most toxic species of Atelopus, with the skin of a single individual containing enough toxins to kill 1,200 20g mice (Savage 2002). Zetekitoxin AB, the major alkaloid in Atelopus zeteki's skin extracts, is an analog of saxitoxin and an extremely potent blocker of voltage-dependent sodium channels (Yotsu-Yamashita et al. 2004). Atelopus zeteki is currently the only known amphibian with saxitoxin-analog activity, producing zetekitoxin C as in addition to zekekitoxin AB (Yotsu-Yamashita et al. 2004). It has been hypothesized that zetekitoxin production requires the presence of symbiotic bacteria, as various forms of bacteria (marine, anaerobic, and cyanobacteria) are known to produce saxitoxin (Daly 2004; Yotsu-Yamashita et al. 2004).

This species appears to undergo an ontogenetic change in color, from cryptic green and black coloration in new and recently metamorphosed frogs and juveniles, to aposematic bright yellow, or yellow and black, in subadults and adults. Lindquist and Hetherington (1998b) hypothesized that this may parallel the acquisition of skin toxicity. They reported that metamorphs and young juveniles were secretive, unlike the adults which moved about openly (Lindquist and Hetherington 1998b).

The genus Atelopus, with 113 described and putative species, appears to be the most threatened clade of amphibians. At least 30 species appear to be extinct, having been missing from all known localities for at least 8 years. Only 52 of the surviving species have sufficient data with which to evaluate population trends; of these, 81% (42 of 52) have population sizes that have been reduced by at least half. Higher-elevation species (those living at least 1000 m asl) have been hit the worst, with 75% (21 of 28) having disappeared entirely. Chytridiomycosis is thought to be a primary factor in the decline and disappearance of species in this genus. Habitat loss has occurred within the ranges of many Atelopus species, but does not appear to be a major factor in the decline of most Atelopus species; 22 species declined despite occurring in protected areas. Many Atelopus species are local endemics, putting them at particular risk of extinction, with at least 26 species known only from a single population inhabiting a narrow altitudinal range (La Marca et al. 2005).

Atelopus zeteki is possibly extinct in the wild, with frogs having been removed to captive breeding facilities in 2006, to protect them against possible death from infection with Batrachochytrium dendrobatidis (Bd). The BBC filmed these frogs courting, wrestling, and semaphoring in the wild shortly before removal. The amphibian chytrid fungus (Batrachochytrium dendrobatidis, or Bd) is spreading through Central America, decimating frog populations (Lips et al. 2006), and overtook the study location soon after the filming.

Richards-Zawacki (2010) has shown that behavioral thermoregulation may be an important mechanism by which this species (and possibly other amphibians as well) can combat Bd infection. Body temperatures were collected before and during a Bd epidemic in Panama. Average body temperature was higher during the epidemic, regardless of air temperature, and this influenced the prevalence of chytrid fungal infection (Richards-Zawacki 2010).


Crump, M.L. (1988). ''Aggression in Harlequin Frogs: male-male competition and a possible conflict of interest between the sexes.'' Animal Behaviour, 36(4), 1064-1077.

Daly, J. W. (2004). ''Marine toxins and nonmarine toxins: convergence or symbiotic organisms?'' Journal of Natural Products, 67, 1211-1215.

Dunn, E. R. (1933). ''Amphibians and reptiles from El Valle de Anton, Panama.'' Occasional Papers of the Boston Society of Natural History, 8, 65-79.

Karraker, N. E., Richards, C. L., and Ross, H. L. (2006). ''Reproductive ecology of Atelopus zeteki and comparisons to other members of the genus.'' Herpetological Review, 37(3), 284-288.

La Marca, E., Lötters, S., Puschendorf, R., Ibáñez, R., Rueda-Almonacid, J. V., Schulte, R., Marty, C., Castro, F., Manzanilla-Puppo, J., García-Pérez, J. E., Bolaños, F., Chaves, G., Pounds, J. A., Toral, E., and Young, B. E. (2005). ''Catastrophic population declines and extinctions in neotropical harlequin frogs (Bufonidae: Atelopus).'' Biotropica, 37(2), 190-201.

Lindquist, E. D. and Hetherington, T. E. (1998). ''Semaphoring in an earless frog: the origin of a novel visual signal.'' Animal Cognition, 1, 83-87.

Lindquist, E. D. and Hetherington, T. E. (1998). ''Tadpoles and juveniles of the Panamanian Golden Frog, Atelopus zeteki (Bufonidae), with information on development of coloration and patterning.'' Herpetologica, 54(3), 370-376.

Lindquist, E. D., and Hetherington, T. E. (1996). ''Field studies on visual and acoustic signaling in the ''earless'' Panamanian Golden Frog, Atelopus zeteki.'' Journal of Herpetology, 30(3), 347-354.

Lips, K. R., Brem, F., Brenes, R., Reeve, J. D., Alford, R. A., Voyles, J., Carey, C., Livo, L., Pessier, A. P., and Collins, J. P. (2005). ''Emerging infectious disease and the loss of biodiversity in a Neotropical amphibian community.'' Proceedings of the National Academy of Sciences, 103(9), 3165-3170.

Poole, V. (2006). Golden Frog Husbandry Manual, 2nd ed. [Internet PDF]. Denver: Denver Zoological Foundation's Project Golden Frog. Retrieved 2 October 2007, from

Richards-Zawacki, C. L. (2010). ''Thermoregulatory behaviour affects prevalence of chytrid fungal infection in a wild population of Panamanian golden frogs.'' Proceedings of the Royal Society B, 277, 519-528.

Savage, J. M. (2002). The Amphibians and Reptiles of Costa Rica. University of Chicago Press, Chicago and London.

Savage, J.M. (1972). ''The harlequin frogs, genus Atelopus, of Costa Rica and western Panama.'' Herpetologica, 28(2), 77-94.

Stuart, S., Hoffmann, M., Chanson, J., Cox, N., Berridge, R., Ramani, P., and Young, B. (eds) (2008). Threatened Amphibians of the World. Lynx Edicions, IUCN, and Conservation International, Barcelona, Spain; Gland, Switzerland; and Arlington, Virginia, USA.

Yotsu-Yamashita, M., Kim, Y.H., Dudley, Jr., S.C., Choudhary, G., Pfahnl, A., Oshima, Y., and Daly, J.W. (2004). ''The structure of zetekitoxin AB, a saxitoxin analog from the Panamanian golden frog Atelopus zeteki: a potent sodium-channel blocker.'' Proceedings of the National Academy of Sciences of the United States of America, 101(13), 4346-4351.

Written by Christin Hong (cmhong AT, Museum of Vertebrate Zoology; University of California, Berkeley
First submitted 2007-10-10
Edited by Kellie Whittaker (2010-01-13)

Species Account Citation: AmphibiaWeb 2010 Atelopus zeteki: Panamanian Golden Frog <> University of California, Berkeley, CA, USA. Accessed Apr 25, 2017.

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Citation: AmphibiaWeb. 2017. <> University of California, Berkeley, CA, USA. Accessed 25 Apr 2017.

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