Overview

Comprehensive Description

Description

Phyllobates bicolor is a small frog, with males reaching an adult size of 32.1-39.5 mm and females reaching 35.7-42.7 mm (Myers et al. 1978). The skin is smooth (Silverstone 1976). Both premaxillary and maxillary teeth are present (Silverstone 1976). The first finger is longer than the second, and the digits have expanded discs (Silverstone 1976). Toes lack webbing (Silverstone 1976).

Phyllobates bicolor color patterning is very striking. The dorsum and sides are a uniform golden yellow or orange, as well as the dorsal surfaces of the upper arm and thigh (Myers et al. 1978). In contrast, the dorsal surfaces of the forearm and calf are black, and may or may not have dense yellow (or sometimes blue) spotting (Myers et al. 1978). The ventrum may be completely black, or washed with light orange, light gold, or bluish green (Myers et al. 1978). There is occasionally a black patch on the throat (Silverstone 1976). The tympanum is partly yellow-orange and partly black (Silverstone 1976). In some individuals, the tip of the snout is black (Silverstone 1976). Irises are black or reddish-brown (Silverstone 1976).

This species, like P. terribilis, exhibits an ontogenetic color change; juveniles are dark brown to black in color, with two yellowish dorsolateral bands. As the frogs reach maturity, the dorsolateral stripes disappear, and the frogs become more brightly colored. In contrast, the juvenile pattern of light stripes on a dark background is retained into adulthood in other members of the P. bicolor group, P. aurotaenia, P. lugubris and P. vittatus (Myers et al. 1978; Silverstone 1976).

Phyllobates bicolor closely resembles P. terribilis, but P. bicolor is smaller in size and has legs and venter of a different hue than the body color (Myers et al. 1978).
 

As is true of other species in the genus Phyllobates, this species produces batrachotoxins. However, captive-born and bred dendrobatid frogs lack toxicity, since the toxins are acquired at least in part from dietary sources such as ants, mites or beetles (Daly et al. 1980; Daly et al. 1992; Dumbacher et al. 2004). In contrast, the toxins persist in wild-caught animals even when they are maintained in captivity (Daly et al. 1978).

Myers et al. (1978) have speculated that there might be either hybridization or a cline between P. bicolor and P. aurotaenia in the upper San Juan drainage, due to the intermediate size and coloration of the Phyllobates found there.

  • Silverstone, P.A. (1976). ''A revision of the poison arrow frogs of the genus Phyllobates Bibron in Sagra (Family Dendrobatidae).'' Natural History Museum of Los Angeles County Science Bulletin, 27, 1-53.
  • Zimmermann, H. (1989). ''Conservation studies on the 'dart-poison' frogs Dendrobatidae in the field and in captivity.'' International Zoo Yearbook, 28, 31-44.
  • Myers, C. W., Daly, J. W., and Malkin, B. (1978). ''A dangerously toxic new frog (Phyllobates) used by Emberá Indians of Western Colombia, with discussion of blowgun fabrication and dart poisoning.'' Bulletin of the American Museum of Natural History, 161, 307-366.
  • Daly, J. W., Myers, C. W., Warnick, J. E., and Albuquerque, E. X. (1980). ''Levels of batrachotoxin and lack of sensitivity to its action in poison-dart frogs (Phyllobates).'' Science, 208, 1383-1385.
  • Daly, J.W., Secunda, S.I., Garraffo, H.M., Spande, T.F., Wisnieski, A., Nishihara, C., and Cover, J.F. (1992). ''Variability in alkaloid profiles in neotropical poison dart frogs (Dendrobatidae): genetic versus environmental determinants.'' Toxicon, 30, 887-898.
  • Dumbacher, J.P., Wako, A., Derrickson, S.R., Samuelson, A., Spande, T.F., and Daly, J.W (2004). ''Melyrid beetles (Choresine): a putative source for the batrachotoxin alkaloids found in poison-dart frogs and toxic passerine birds.'' Proceedings of the National Academy of Sciences of the United States of America, 101, 15857-15860.
  • IUCN, Conservation International, and NatureServe. (2006). Global Amphibian Assessment: Phyllobates bicolor. www.globalamphibians.org. Accessed on 7 May 2008.
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Distribution

Distribution and Habitat

The Black Leg Poison Dart Frog lives in the tropical rain forests of Colombia, on the western side of the northern part of the Cordillera Occidental, between 25-1,525 m above sea level. It occurs in the upper Atrato and San Juan drainages, the Río Raposo, and headwaters of the Río Sipí, in the Cordillera Occidental. This species inhabits the forest floor (Silverstone 1976; Myers et al. 1978). It is reported to survive in logged forest but not open habitat (IUCN 2006).
  • Silverstone, P.A. (1976). ''A revision of the poison arrow frogs of the genus Phyllobates Bibron in Sagra (Family Dendrobatidae).'' Natural History Museum of Los Angeles County Science Bulletin, 27, 1-53.
  • Zimmermann, H. (1989). ''Conservation studies on the 'dart-poison' frogs Dendrobatidae in the field and in captivity.'' International Zoo Yearbook, 28, 31-44.
  • Myers, C. W., Daly, J. W., and Malkin, B. (1978). ''A dangerously toxic new frog (Phyllobates) used by Emberá Indians of Western Colombia, with discussion of blowgun fabrication and dart poisoning.'' Bulletin of the American Museum of Natural History, 161, 307-366.
  • Daly, J. W., Myers, C. W., Warnick, J. E., and Albuquerque, E. X. (1980). ''Levels of batrachotoxin and lack of sensitivity to its action in poison-dart frogs (Phyllobates).'' Science, 208, 1383-1385.
  • Daly, J.W., Secunda, S.I., Garraffo, H.M., Spande, T.F., Wisnieski, A., Nishihara, C., and Cover, J.F. (1992). ''Variability in alkaloid profiles in neotropical poison dart frogs (Dendrobatidae): genetic versus environmental determinants.'' Toxicon, 30, 887-898.
  • Dumbacher, J.P., Wako, A., Derrickson, S.R., Samuelson, A., Spande, T.F., and Daly, J.W (2004). ''Melyrid beetles (Choresine): a putative source for the batrachotoxin alkaloids found in poison-dart frogs and toxic passerine birds.'' Proceedings of the National Academy of Sciences of the United States of America, 101, 15857-15860.
  • IUCN, Conservation International, and NatureServe. (2006). Global Amphibian Assessment: Phyllobates bicolor. www.globalamphibians.org. Accessed on 7 May 2008.
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Range Description

This species occurs on the western slopes of the Cordillera Occidental in Colombia, in Risaralda, Choco, Valle del Cauca, and Cauca Departments, between 500 and 1,500m asl.
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Geographic Range

Phyllobates bicolor inhabits the tropical rain forests of Central and South America. The Choco Indians report finding them most commonly in the Pacific River area of Western Colombia (National Aquarium in Baltimore, 1987).

Biogeographic Regions: neotropical (Native )

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Physical Description

Morphology

Physical Description

Phyllobates bicolor is typically golden-yellow in color and has black flecks on its hind legs. However, the color pattern varies widely. All of the poison-dart frogs have very bright aposematic coloration. This is used as a defense mechanism to warm potential predators of there extreme toxicity. These skin toxins are produced by special poison glands which are scattered all over the animal's body (National Aquarium in Baltimore, 1987). Phyllobates bicolor has terminal discs on its digits that allow them to climb well in shrubs and up mossy tree trunks (Mattison, 1987). Unlike males of most frog species, which are smaller than the females, male poison-dart frogs are relatively the same size when compared to the females (Badger et al, 1995).

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Ecology

Habitat

Habitat and Ecology

Habitat and Ecology
It lives in humid lowland and montane forests, usually occurring near streams, and can survive in logged forest, but not in open areas. The eggs are laid on the ground and the male transports the larvae to streams.

Systems
  • Terrestrial
  • Freshwater
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Habitat

Phyllobates bicolor are inhabitants of the tropical rain forests. They live colonially on the forest floor, often near small streams. They do well in the moist, humid conditions that the rainforests provide. The temperature rarely falls below 80 degrees Fahrenheit and the minimal annual rainfall is about 80 inches. Some areas may recieve as much as 400 inches of rain per year. This constant warmth and rainfall keep the habitat of Phyllobates bicolor green all year long (National Aquarium of Baltimore, 1987).

Terrestrial Biomes: rainforest

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Trophic Strategy

Food Habits

Phyllobates bicolor is primarily carnivorous. Adults feed on ants, termites, tiny beetles, and other small leaf litter arthropods. They capture their prey using their long, sticky retractable tongue. The young tadpoles may eat each other if placed together in a small area, but mostly they feed on insect larvae, detritis, and on unfertilized eggs left by a visiting female (National Aquarium in Baltimore, 1987).

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Life History and Behavior

Reproduction

Reproduction

Most populations of Phyllobates bicolor breed continuously througout the rainy season, some every other month or even more frequently. In order to attract a female, the male will sit on a leaf and call by trilling or buzzing. This may go on for several days. Once a female is attracted, the mating pair must find a suitable location to lay their eggs. In some species, the male will select a location for the eggs prior to obtaining a mate. They are usually laid in a moist place, such as, in the leaf litter, under rocks, or even on certain rain forest plants (National Aquarium in Baltimore, 1987). Phyllobates bicolor have external fertilization with the male fertilizing the eggs as the female deposits them. During amplexus, the male has to clasp his mate under her chin instead of around her waist due to the similarities in size between the males and females (Badger et al, 1995). The female lays from 4-30 eggs in a jelly-like mass, which keeps them moist. Then, they are usually gaurded by either parent until they are ready to hatch. At this point in their development, water is required. The attending parent will squat in the gelatinous mass and allow the young to wriggle up his/her legs and onto their back. The larvae may remain on the adult's back for a few minutes or for several hours. The young are firmly attached by a mucous secretion which is only broken down by the immersion in water (Mattison, 1987). The parent will take the tadpoles to a suitable body of water where they are able to continue their development. This may consist of a puddle in a tree hole or a water holding plant such as a bromelaid or the leaf axils of palms or aroids. It takes about 3 weeks for the tadpoles to complete metamorphosis. After this time, the young will return back to their natural arboreal or terrestrial habitat (Badger et al, 1995).

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Molecular Biology and Genetics

Molecular Biology

Barcode data: Phyllobates bicolor

The following is a representative barcode sequence, the centroid of all available sequences for this species. 

 
There is 1 barcode sequence available from BOLD and GenBank.   Below is the sequence of the barcode region Cytochrome oxidase subunit 1 (COI or COX1) from a member of the species.  See the BOLD taxonomy browser for more complete information about this specimen.  Other sequences that do not yet meet barcode criteria may also be available.
 
GBAP0346-06|DQ502884|Phyllobates bicolor| ---------------------------------------ACCTTGTACCTAGTGTTCGGCGCATGAGCCCGGATGGTAGGTACGGCCCTT---AGCCTATTAATTCGAGCAGAGCTAAGTCAACCCGGCTCTTTGCTAGGTGAT---GATCAAATTTATAATGTAATCGTCACCGCCCACGCCTTCGTAATAATTTTTTTTATGGTTATGCCAATTCTTATTGGTGGGTTCGGAAACTGACTTGTTCCTTTGATA---ATTGGGGCCCCTGACATAGCCTTCCCTCGAATGAACAACATAAGTTTTTGACTTCTCCCCCCCTCTTTTCTTCTCCTGTTAGCTTCAGCAGGGGTTGAAGCAGGCGCAGGCACAGGTTGGACAGTTTATCCCCCTCTCGCAAGCAACCTAGCCCATGCCGGACCATCAGTAGATTTA---ACAATTTTTTCACTCCATTTGGCTGGAGTGTCATCTATTCTAGGGGCAATTAATTTTATTACTACTACCCTAAACATAAAACCCCCTTCACTAACACAATATCAAACCCCCCTATTTGTGTGGTCCGTCTTAATCACCGCTATTCTCCTTCTCCTTTCCCTTCCAGTCTTGGCCGCA---GGCATTACAATGCTACTTACTGACCGAAACTTAAACACAACCTTCTTCGACCCCGCCGGAGGTGGGGACCCAGTTCTTTACCAACACTTA-------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------  
-- end --

Download FASTA File
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Statistics of barcoding coverage: Phyllobates bicolor

Barcode of Life Data Systems (BOLDS) Stats
Public Records: 1
Species: 1
Species With Barcodes: 1

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Conservation

Conservation Status

IUCN Red List Assessment


Red List Category
NT
Near Threatened

Red List Criteria

Version
3.1

Year Assessed
2004

Assessor/s
Wilmar Bolívar, Stefan Lötters

Reviewer/s
Global Amphibian Assessment Coordinating Team (Simon Stuart, Janice Chanson, Neil Cox and Bruce Young)

Justification
Listed as Near Threatened since although its Extent of Occurrence is less than 20,000 km2 and its habitat is declining, thus making the species close to qualifying for Vulnerable, it probably occurs in more than ten locations, and its range is probably not yet severely fragmented.
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Conservation Status

The pet trade and the destruction of the tropical rain forests are leading to a decline in the Dendrobatids such as Phyllobates bicolor. When the rain forests disappear, so do the animals that inhabit it (National Aquarium in Baltimore, 1987). One of the most spellbinding exhibits of live poison-dart frogs frogs in the United States is located at the National Aquarium in Baltimore, Maryland. Herpetologists there have had success breeding as many as 20 species, but they have also encountered a potential problem. Poison-dart frogs that are born in captivity do not secrete skin toxins. Scientists aren't sure why, but they speculate that the absence of certain bacteria in the environment or perhaps something missing in their diet may be the reason (Badger et al, 1995). The rain forest exhibit at the National Aquarium exists to make the public aware of the diversity of life found within the rain forests throughout the world. Hopefully, this awareness will create a desire to help protect the habitat of species like Phyllobates bicolor (National Aquarium in Baltimore, 1987).

CITES: appendix ii

IUCN Red List of Threatened Species: near threatened

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Population

Population
It is an abundant species.

Population Trend
Decreasing
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Life History, Abundance, Activity, and Special Behaviors

Like other dendrobatids, Phyllobates bicolor are diurnal and are very active. Little has been published on the reproductive behavior of this species in the wild. Zimmermann (1989) has published sonograms of P. bicolor calls, and reports that in captivity, P. bicolor, males initiate courtship by giving a "long-range" courtship call. The female then follows the male to a covered egg deposition site. Once the female approaches within 8 cm, the male emits a "short-range" courtship croak call, ceasing before the female oviposits. Circling and body-anal touching was observed but not amplexus. In captivity, a single female may lay up to three clutches of 12-20 eggs per month. The male moistens the clutch at irregular intervals (hydric brooding). Tadpoles hatch in about 14 days, after which the male transports them to a water-filled brooding site (Zimmermann 1989).

  • Silverstone, P.A. (1976). ''A revision of the poison arrow frogs of the genus Phyllobates Bibron in Sagra (Family Dendrobatidae).'' Natural History Museum of Los Angeles County Science Bulletin, 27, 1-53.
  • Zimmermann, H. (1989). ''Conservation studies on the 'dart-poison' frogs Dendrobatidae in the field and in captivity.'' International Zoo Yearbook, 28, 31-44.
  • Myers, C. W., Daly, J. W., and Malkin, B. (1978). ''A dangerously toxic new frog (Phyllobates) used by Emberá Indians of Western Colombia, with discussion of blowgun fabrication and dart poisoning.'' Bulletin of the American Museum of Natural History, 161, 307-366.
  • Daly, J. W., Myers, C. W., Warnick, J. E., and Albuquerque, E. X. (1980). ''Levels of batrachotoxin and lack of sensitivity to its action in poison-dart frogs (Phyllobates).'' Science, 208, 1383-1385.
  • Daly, J.W., Secunda, S.I., Garraffo, H.M., Spande, T.F., Wisnieski, A., Nishihara, C., and Cover, J.F. (1992). ''Variability in alkaloid profiles in neotropical poison dart frogs (Dendrobatidae): genetic versus environmental determinants.'' Toxicon, 30, 887-898.
  • Dumbacher, J.P., Wako, A., Derrickson, S.R., Samuelson, A., Spande, T.F., and Daly, J.W (2004). ''Melyrid beetles (Choresine): a putative source for the batrachotoxin alkaloids found in poison-dart frogs and toxic passerine birds.'' Proceedings of the National Academy of Sciences of the United States of America, 101, 15857-15860.
  • IUCN, Conservation International, and NatureServe. (2006). Global Amphibian Assessment: Phyllobates bicolor. www.globalamphibians.org. Accessed on 7 May 2008.
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Threats

Threats

Major Threats
The major threats are: deforestation due to agricultural development, cultivation of illegal crops, logging, and human settlement; introduction of alien predatory fish in streams; and pollution resulting from the spraying of illegal crops. It occurs in the international pet trade, but it is not known to what extent this poses a threat to the species. Chytridiomycosis might be a potential future threat.
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Life History, Abundance, Activity, and Special Behaviors

It occurs in one protected area, the Parque Nacional Natural Farallones de Cali. Major threats include habitat alteration due to deforestation for agriculture and logging, and human settlement; pollution from spraying illegal crops; and introduction of non-native predatory fish. Collection for the international pet trade occurs but it is difficult to assess the extent of this threat. Chytridiomycosis may be a potential future threat (IUCN 2006).
  • Silverstone, P.A. (1976). ''A revision of the poison arrow frogs of the genus Phyllobates Bibron in Sagra (Family Dendrobatidae).'' Natural History Museum of Los Angeles County Science Bulletin, 27, 1-53.
  • Zimmermann, H. (1989). ''Conservation studies on the 'dart-poison' frogs Dendrobatidae in the field and in captivity.'' International Zoo Yearbook, 28, 31-44.
  • Myers, C. W., Daly, J. W., and Malkin, B. (1978). ''A dangerously toxic new frog (Phyllobates) used by Emberá Indians of Western Colombia, with discussion of blowgun fabrication and dart poisoning.'' Bulletin of the American Museum of Natural History, 161, 307-366.
  • Daly, J. W., Myers, C. W., Warnick, J. E., and Albuquerque, E. X. (1980). ''Levels of batrachotoxin and lack of sensitivity to its action in poison-dart frogs (Phyllobates).'' Science, 208, 1383-1385.
  • Daly, J.W., Secunda, S.I., Garraffo, H.M., Spande, T.F., Wisnieski, A., Nishihara, C., and Cover, J.F. (1992). ''Variability in alkaloid profiles in neotropical poison dart frogs (Dendrobatidae): genetic versus environmental determinants.'' Toxicon, 30, 887-898.
  • Dumbacher, J.P., Wako, A., Derrickson, S.R., Samuelson, A., Spande, T.F., and Daly, J.W (2004). ''Melyrid beetles (Choresine): a putative source for the batrachotoxin alkaloids found in poison-dart frogs and toxic passerine birds.'' Proceedings of the National Academy of Sciences of the United States of America, 101, 15857-15860.
  • IUCN, Conservation International, and NatureServe. (2006). Global Amphibian Assessment: Phyllobates bicolor. www.globalamphibians.org. Accessed on 7 May 2008.
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Management

Conservation Actions

Conservation Actions
It occurs in Parque Nacional Natural Farallones de Cali. Management practices that could allow a commercial, sustainable harvest of this species should be investigated. Decree INDERENA No. 39 of 9 July, 1985, forbids the collection of Phyllobates spp. from the wild in Colombia for breeding (or other) purposes. It is listed on CITES Appendix II.
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Relevance to Humans and Ecosystems

Benefits

Economic Importance for Humans: Positive

Native peoples in Colombia collect brightly colored frogs and use their poisonous skin secretions to coat the ends of hunting arrows. This method, first reported by British naval captain, Charles Stuart Cochrane, is highly effective in hunting jaguars, monkeys, birds, and small game animals. These skin toxins are of great interest to medical researchers because of their remarkable potency. The batrachotoxins secreted by Phyllobates bicolor are especially valuable for medical science and the study of anesthetics, muscle relaxants, cardiac stimulants, and the control of rapid or irregular heartbeats (Badger et al, 1995).

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Economic Importance for Humans: Negative

Scientists believe that the skin toxins of Phyllobates bicolor are so toxic that .0000004 ounces may be enough to kill a human being. Toxins from these frogs work quickly, attacking the nerves and muscles. Nerve cells can no longer transmit impulses and muscle cells remain in an activated, contracted state. The result is death by respiratory or muscular paralysis (Badger et al, 1995).

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Risks

Relation to Humans

Phyllobates bicolor is one of only three species of frog (P. terribilis, P. aurotaenia, and P. bicolor) that have been documented as used by humans to poison darts. All are from the Pacific versant of Colombia, and used by various tribes of the Chocó Indians in western Colombia. All three species have high levels of batrachotoxins, with P. terribilis by far the most toxic and the other two species approximately equal in toxicity to each other. Phyllobates terribilis contains 700-1900 micrograms of batrachotoxin-homobatrachotoxin per frog, whereas P. bicolor contains 17-56 micrograms of combined toxins per frog. Batrachotoxin-containing skin secretions for poisoning dart tips are obtained either by simply rubbing the tip on the live frog's back (P. terribilis), or impaling the frog and also sometimes heating it (P. bicolor and P. aurotaenia) (Myers et al. 1978).
  • Silverstone, P.A. (1976). ''A revision of the poison arrow frogs of the genus Phyllobates Bibron in Sagra (Family Dendrobatidae).'' Natural History Museum of Los Angeles County Science Bulletin, 27, 1-53.
  • Zimmermann, H. (1989). ''Conservation studies on the 'dart-poison' frogs Dendrobatidae in the field and in captivity.'' International Zoo Yearbook, 28, 31-44.
  • Myers, C. W., Daly, J. W., and Malkin, B. (1978). ''A dangerously toxic new frog (Phyllobates) used by Emberá Indians of Western Colombia, with discussion of blowgun fabrication and dart poisoning.'' Bulletin of the American Museum of Natural History, 161, 307-366.
  • Daly, J. W., Myers, C. W., Warnick, J. E., and Albuquerque, E. X. (1980). ''Levels of batrachotoxin and lack of sensitivity to its action in poison-dart frogs (Phyllobates).'' Science, 208, 1383-1385.
  • Daly, J.W., Secunda, S.I., Garraffo, H.M., Spande, T.F., Wisnieski, A., Nishihara, C., and Cover, J.F. (1992). ''Variability in alkaloid profiles in neotropical poison dart frogs (Dendrobatidae): genetic versus environmental determinants.'' Toxicon, 30, 887-898.
  • Dumbacher, J.P., Wako, A., Derrickson, S.R., Samuelson, A., Spande, T.F., and Daly, J.W (2004). ''Melyrid beetles (Choresine): a putative source for the batrachotoxin alkaloids found in poison-dart frogs and toxic passerine birds.'' Proceedings of the National Academy of Sciences of the United States of America, 101, 15857-15860.
  • IUCN, Conservation International, and NatureServe. (2006). Global Amphibian Assessment: Phyllobates bicolor. www.globalamphibians.org. Accessed on 7 May 2008.
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Wikipedia

Black-legged dart frog

The black-legged dart frog (Phyllobates bicolor), also known as the bicolored dart frog or neari in Choco, is the second-most toxic of the wild poison dart frogs. This species obtained its name due to its normally yellow or orange body with black or dark blue hindlegs and forelimbs below the elbow. It lives in the lowland forests in the Chocó area in western Colombia, along the San Juan River, although some populations live further South in Quebrada Guangui. The frogs from Quebrada Guangui bear a striking resemblance to the yellow or orange forms of Phyllobates terribilis, and are sometimes confused for them by hobbyists.

In this species, the male transports tadpoles adhering on its back.[1]

Contents

Description

P. bicolor is one of the largest poison dart frogs. Males can reach a length of 45–50 mm from snout to vent, while the slightly larger females reach 50–55 mm in length from snout to vent. P bicolor ranges in color from earthy orange to pure yellow in coloration, often with a blue or black tinge on their legs, hence their name. They are smaller and more slender than their close relative, Phyllobates terribilis, and can resemble juvenile or subadult P. terribilis frogs. They also bear a resemblance to D. leucomelas, particularly the "netted" color morph of D. leucomelas.

Phyllobates bicolor01.jpg

Toxicity

While its toxicity is weaker than P. terribilis, P. bicolor is still a highly toxic animal, one of the few frogs confirmed to have caused human fatalities. Just 150 micrograms of its poison is enough to kill an adult human. This frog is often heated over a flame to make it "sweat" the liquid poison for hunting darts. The poison causes death by respiratory and muscular paralysis. Research is being conducted to determine medicinal uses for this batrachotoxin. As with all dart frogs, captive-raised individuals are not toxic; the animals require chemicals found only in their wild food sources, mainly insects. In captivity, these chemicals are not available to them from their food sources.

Behavior

P. bicolor can sometimes be kept in groups in captivity.

Like many of the Phyllobates genus, P. bicolor is mostly terrestrial, only taking to the trees when rearing young. Most are solitary animals, however wild groups can be found occasionally. Unlike many frog species, both males and females can be vocal, producing high-pitched, bird-like calls. The black-legged poison dart frog is mostly diurnal, retreating into the cover of the leaf litter at night. While most individuals are solitary, during the wet season, P. bicolor frogs, like all dendrobatids, gather in large breeding groups. One of the more dedicated of parents among anurans, P. bicolor males carry their tadpoles on their backs. The tadpoles stick to the mucus on the backs of their fathers, and are transported to puddles. There they are fed and protected until they become froglets, at which point they are completely independent, and leave to begin their adult lives.

Captive care

Care for P. bicolor is similar to Phyllobates terribilis, except P. bicolor can be kept in a slightly smaller enclosure. Both males and females of this species can be vocal.

References

  1. ^ Hickman, Cleveland P. Jr., et al. (2006). Integrated Principles of Zoology. McGraw-Hill New York. 

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