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Description ( Inglês )

fornecido por AmphibiaWeb articles
Lithodytes lineatus is a leaf-litter frog found primarily in the Amazon. Adult female L. lineatus are have a total length of 38.1 - 52.0 mm and significantly larger than adult males, who range from 34.9 - 47.0mm. When viewed from both the profile and above, its snout is rounded. The distinct tympanum is about the same diameter as its eye. The dorsum skin is finely speckled and the venter skin is smooth. Finger webbing is absent, and its first finger is longer than the second. The snout-vent length of juveniles collected in Rondonia state, northwestern Brazil between April 2001 and March 2002 ranged from 19.6 - 35.9 mm (Duellman 2005; Bernarde and Kokubum 2009).Tadpoles in Gosner Stage 34 typically have a body length of 18.1 mm. In dorsal view their body is elongated ovoid and is the widest (wider than high) at one-third of its length. It’s a total length of 47.4mm. The snout is bluntly rounded in profile view, but truncate in dorsal view. Its eyes are situated dorsally, are slightly anterodorsally, and directed laterally. The nares are situated about midway between the eyes and the tip of the snout and the spiracle is sinistral below the midline of the body. The interorbital distance is about four times the diameter of the eye. The spiracular tube started slightly posterior to the mid-length of the body and is attached to the body in its entirety. The spiracular tube’s opening is directed posterodorsally. The vent tube is moderately long, medial, and attached to the ventral fin with its tip free. The caudal musculature is highest at about one-third of the length of the tail and is moderately robust. It gradually narrows posteriorly and it ends just before the rounded tip of the tail. The dorsal fin and ventral fin start at the bottom of the tail. The dorsal fin is highest around mid-length while the ventral fin is highest at about one-third the length of the tail and is equal to the height of the dorsal fin at this point. In the middle of the tail, both fins are shallower than the caudal musculature and gradually narrow to come to a rounded tip. The oral disc is anteroventral and the anterior labium is bare; everywhere else there is a single row of long marginal papillae. There are no submarginal papillae. It’s jaw sheaths are finely serrate, broadly arched and sender. The labial tooth row formula (LTRF) is 0/1; the LTRF and the presence of jaw sheaths are variable, 0/0 to 2(2)/3(1) (Duellman 2005).Lithoydytes and Phyllobates fermoralis are two terrestrial species that may represent a case of amphibian (Batesian and Mullerian) mimicry. They both have yellow dorsolateral lines in almost the same position and have similar dorsal coloration and lash color. Lithodytes lineatus has wider dorsolateral lines than Phyllobates fermoralis (Dendrobatidae). Lithodytes Lineatus also has an orange stripe that starts at the groin and extends to its posterior face. It has dark tan limbs with dark spots on the proximal part of the thigh and black dorsal coloration with a slight tan coloring. Phyllobates femoralis has a black and white mottled venter and a cream ventro-lateral stripe that L. lineatus is missing. Pyllobates is known for having toxic skin secretions while L. lineatus has studded dorsal surfaces and granular tubercles which could suggest that it may also have dermal secretions used for protection (Nelson and Miller 1971). In life, L. lineatus has a black dorsum and flanks with a thick yellow stripe that extends from their snout to their to the groin. The belly and ventral surfaces of the hind limbs are grey, throat and chest are brown, and the upper arms are tan. Lithodytes lineatus has red spots on the posterior surfaces of thighs and there is a large red spot on the groin. The iris is a dark coppery bronze and fine black reticulations are present (Duellman 2005; Nelson and Miller 1971).Alive, the L. lineatus tadpole body is bright pink and has a short, white, metallic mid-dorsal stripe. Its fin is translucent pink and the color of the caudal musculature is similar to the body but is less intense distally (Duellman 2005).Lithodytes lineatus was previously known under the genus Lithodytes (Bernarde and Kokubum 2009). It was also first described as Rana lineata (Schneider 1799).This species is often considered to be a mimic of some Aromobatids and Dendrobatids because of its coloration and juvenile diurnal activity. The largest male of this species was found in Espigão do Oeste while the largest female was found in Cecília, Ecuador (Bernarde and Kokubum 2009). Lithodytes lineatus is synonomous with Leptodactylus lineatus (Kwet 2007)(image, http://amphibiaweb.org/images/amazing/amazing_logo.jpg) Featured in Amazing Amphibians on 1 April 2013 (http://amphibiaweb.org/amazing_amphibians/20130401_Lithodytes_lineatus.html)

Referências

  • Bernarde, P.S., Kokubum, M.N. de C. (2009). ''Seasonality, age structure and reproduction of Lithodytes (Lithodytes) lineatus (Anura, Leptodactylidae) in Rondônia state, southwestern Amazon, Brazil.'' Iheringia. Série Zoologia, 99(4), 368-372.
  • Kwet, A. 2007. Bioacoustic variation in the genus Adenomera in southern Brazil, with revalidation of Leptodactylus nanus Müller, 1922 (Anura, Leptodactylidae). Mitt. Mus. Nat.kd. Berl., Zool. Reihe 83(Supplement): 56–68
  • La Marca, E., Azevedo-Ramos, C., Coloma, L.A., Ron, S., Hardy, J. 2010. Lithodytes lineatus. In: IUCN 2012. IUCN Red List of Threatened Species. Version 2012.2. Downloaded on 05 February 2013.
  • Nelson, C., Miller, G.A. 1971. A possible case of mimicry in frogs. Herptelogical Review. 3(6):109
  • Rödel, M.-O. and Braun, U. (1999). ''Associations between anurans and ants in a West African savanna (Anura: Microhylidae, Hyperoliidae and Hymenoptera: Formicidae).'' Biotropica, 31(1), 178-183.
  • Rödel, M.O., Brede, C., Hirschfeld, M., Schmitt, T., Favreau, P., Stöcklin, R., Wunder, C., Mebs, D. (2013). ''Chemical camouflage – a frog’s strategy to coexist with aggressive ants.'' PLOS One, 8, e81950.
  • Schluter, A. Regos, J. 1996. The tadpole of Lithodytes lineatus - with notes on the frog resistance to leaf-cutting ants (Amphibia: Leptodactylidae). Stuttgarter Beitrage zur Naturkunde Ser. A, 536: 1-4
  • Schlüter, A., Löttker, P., and Mebert, K. (2009). ''Use of an active nest of the leaf cutter ant Atta cephalotes (Hymenoptera: Formicidae) as a breeding site of Lithodytes lineatus (Anura: Leptodactylidae).'' Herpetology Notes, 2, 101-105.
  • Schneider, J.G. 1799. Historiae Amphibiorum Naturalis et Literariae, volume 1. Friedrich Frommann, Jena.
  • de Lima Barros, A., López-Lozano, J.L., Lima, A.P. (2016). ''The frog Lithodytes lineatus (Anura: Leptodactylidae) uses chemical recognition to live in colonies of leaf-cutting ants of the genus Atta (Hymenoptera: Formicidae).'' Behavioral Ecology and Sociobiology, 70, 2195-2201.

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Distribution and Habitat ( Inglês )

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Lithodytes lineatus is often considered too rare to find in many studies of anuran habitats, but it is known for being widely distributed in Amazonian forests of Ecuador, Eastern Peru, Brazil, Venezuela, and the Guianas. It is found in both terrestrial and freshwater habitats but is primarily found in tropical rainforests. It can be found below leaf-litter, logs, and other forest cover (La Marca et al. 2012).
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Life History, Abundance, Activity, and Special Behaviors ( Inglês )

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Currently there is not enough information to distinguish proper threats to this species. According to the IUCN, L. lineatus is listed as Least Concern due to its wide distribution, presumably large population, and a possible ability to tolerate a degree of habitat alteration. Its ability to adapt over a long period of time is unknown. There are no current conservation measures being undertaken for this species because it is classified as Least Concern and it is found in many protected areas. In order to know if conservation measures need to be taken, more studies are needed to thoroughly understand this species and what it needs to maintain its stability (La Marca et al. 2012).
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Life History, Abundance, Activity, and Special Behaviors ( Inglês )

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In the past, Lithodytes lineatus has appeared to be a mostly forest dwelling species. Although this species is relatively abundant in Amazonian forests, knowledge of it is limited. What is well known is L. lineatus’ association with leaf cutter ants, Atta cephalotes. This relationship has been suggested to be a true symbiosis, with ant nests having been observed as a breeding site of L. lineatus during the October to March breeding season. Such a relationship has never been reported before. This association often impedes visual encounter surveys because males call from the ant nest burrows. Lithodytes lineatus, sports impressive yellow stripes along its back. Originally thought to be a Batesian mimic of other poison frogs, it turned out that this species is actually toxic, and hence likely to be a Mullerian co-mimic (Prates et al. 2012). Recent research on this species has revealed another fascinating component to its natural history – it chemically mimics ants. This species is typically found living in the nests of leaf-cutter ants (genus Atta), yet does not appear to suffer attacks from the ants, which are generally highly aggressive towards nest intruders. De Lima Barros et al. (2016) tested the hypothesis that the frogs use chemical mimicry, by producing or acquiring a coating of chemicals on their skin that deceives the ants into perceiving them as nest members rather than intruders. They tested individual L. lineatus against four similar species of frogs by confining them with leaf-cutter ants, and found that while all the other species were attacked, L. lineatus individuals were not and made no attempt to escape the ants. The researchers then prepared a skin extract from L. lineatus that they used to coat 10 individuals of another species (10 others were coated with purified water as a control). In contrast to the controls, the frogs coated with L. lineatus skin extract were not attacked by the ants. This provides experimental evidence that chemicals on the skin of L. lineatus provide an effective form of mimicry. Although chemical mimicry is more commonly found in parasitic insects, this is not the first time that such mimicry has been detected in frogs. For example, Rödel and Braun (1999) identified several species of African frogs that appear to chemically mimic ants, and Rödel et al. (2013) identified specific skin peptides that enable the African frog, Phrynomantis microps, to chemically mimic the ponerine ants that this species lives with. The benefits that these frog species derive from living with ants are not yet known, but obvious possibilities include protection from predators, access to a climatically optimal microenvironment inside ant nests, or even access to a food source.Calls of synchronus Lithodytes lineatus males’ have been recorded from inside of the same large nest of these ants, with advertisement calls consisting of a series of short whistles that are produced at a continuous rate of about 90 notes/minute. The notes are in three distinct harmonics at 1300, 2600 (dominant), and 3900Hz and each last about 0.12 seconds long. Egg-bearing females and calling males are often found most frequently between September and February (Duellman 2005; Bernarde and Kokubum 2009; Schlüter et al. 2009).An adult female that was collected in 1986 contained 211 unpigmented eggs with a diameter of 1.5 mm. Although, egg laying has not been observed, eggs have been found in foam nests on water, under pieces of bark in water on a terrarium, or at the mouth of a partially submerged burrow (Duellman 2005). Foam-nests adhere to the roots protruding from the otherwise smooth walls. Tadpoles in this type of nest have been found at all different developmental stages and leave the foam nests between 7-15 days after the nest was built. Tadpoles begin to feed about 3 days after they hatch, but their nutrition needs further investigation as most captive-raised tadpoles that were fed with commercial fish food died within a few weeks. Tadpoles have been found in water filled depressions at the end of a system of underwater burrows with a vertical tunnel directly above the pool that was around 25 cm in diameter. Adult frogs of this species have also been found in pathways in the forest or sitting in hollow logs that didn't show any obvious association to the ant nests (Duellman 2005; Schlüter et al.2009). It has been noted that all L. lineatus’ captured at the entrance of these Atta nests released an aromatic odor. It is suggested that this might be a chemical disguise or repellent to prevent ants, which usually try to kill intruders, from attacking. Experiments have been conducted in which specimens of L. lineatus did not have this odor and were immediately killed by the ants. Leptodctylus lineatus benefit from their association with leaf cutter ants because they can obtain suitable hiding places against predation, experience stable microclimates, and also possibly obtain food from these nests; it is unclear if L. lineatus feeds on invertebrate predators of leaf-cutter ants (Schlüter et al. 2009).The stomach contents of two individuals included nineteen ants making up 54.3% of the number of prey accounting for 8.1% of the volume. Other stomach contents included a cricket (33.9%), an earthworm (22.0%), isopods (12.6%), and insect larvae (12.4%) (Duellman 2005). Lithodytes lineatus has a seasonal recruitment pattern very similar to other species in the Central Amazon that depend on still water for larva development with juvenile recruitment occurring from February to June (the end of the rainy season and the beginning of the dry season). Females appear to reach sexual maturity at 38.1 mm. Mature ovarian egg sizes range from 1.50 to 1.92 mm and egg count ranges from 110 to 328. Egg count has a positive correlation with female snout-vent length (Bernarde and Kokubum 2009).
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Brief Summary ( Inglês )

fornecido por EOL authors

Lithodytes lineatus, the gold-striped frog, also known as the painted ant nest frog, is a fairly common terrestrial leptodactylid widely distributed in Amazonian forests of Ecuador, Eastern Peru, Brazil, Venezuela, and the Guianas. It is the only species in its genus, but molecular studies suggest diverges that indicate a split might be due (de Sá 2014). As it lives and forages under leaf-litter, logs, and other forest cover at forest edges, pastures, and flooded savannah forest, and is mostly active nocturnally, it is not commonly noticed and little is known about its ecology (La Marca et al. 2012).

Named for the yellow stripes flanking both sides of their black back, L. lineatus has grey belly, ventrum, and hind limbs, brown throat and chest, and tan upper arms. There are distinguishing red spots on the posterior surfaces of thighs and a large red spot on the groin.Adult female L. lineatus are have a total length of 38.1 - 52.0 mm and significantly larger than adult males, who range from 34.9 - 47.0 mm (Duellman 2005, Nelson and Miller 1971; as cited in Chiachi 2013).

Gold-striped frogs are remarkable in that they frequently associate with leaf cutter ants, Atta cephalotes, in a kind of relationship never before reported in which the frogs use the burrows of ant nests as breeding sites. The relationship was first described from in Peru when synchronous calling was heard from the inside of the ant nests, advertisement calls consisting of a series of short whistles that are produced at a continuous rate of about 90 notes/minute. The notes are in three distinct harmonics at 1300, 2600 (dominant), and 3900Hz and each last about 0.12 seconds long.This relationship benefits the frogs, which receive protected brooding sites with stable temperature and humidity. To protect themselves from attack from the ants, the frogs appear to produce a chemical odor that the ants recognize; frogs and tadpoles with this odor are ignored by the ants.Granular tubercles on their backs may be the source of these protective secretions. Some experimental work showed if the odor is removed from the frogs, the ants immediately attack andkill them.

There is evidence to suggest the L. lineatus/A. cephalotes relationship is a true symbiosis, with potential mutual benefits, as frogs do not appear to eat A. cephalotes ants (although much of their diet appears to be ants of other species), and furthermore the frogs appear to eat predators plaguing the ant nests such as assassin bugs, though further research is necessary to confirm this behavior is significant (Schlüter et al. 2009).

Frog breeding occurs during the rainy season, and adults build foam nests adhered to walls above puddles inside mud ant nest burrows, or at the edge of temporary pools. Into these foam nests females lay some 100-300 unpigmented eggs, 1.5 mm in diameter. The nests house various stages of pink tadpoles (backs crested with a short light strip) where they stay about 15 days. Tadpoles start to feed several days after they leave the nest.

Gold-striped frogs turn out to have multiple protective strategies in addition to their ant mutualism.They show striking resemblance to the toxic dendrobatid frog Phyllobates fermoralis, which also has yellow dorsolateral lines and similar dorsal coloration. Juvenile L. lineatus frogs appear to have diurnal habits (unlike the adults) and Cintra et al. 2014 and Schleuter et al. 2009 suggest this is convincing Batesian mimicry of P. fermoralis giving another protective strategy.Cintra et al. 2014 also point out that L. lineatus shows deimatic “body lifting posture,” yet a third method of defense, in which the frogs lift their rear to show off aposematic coloring, and lift nictitating membrane to protect eyes.

Referências

  • Chiachi, A. 2013 (Edited by A.T. Chang, April 2014). Lithodytes lineatus. AmphibiaWeb. Retrieved July 10 2015 from http://amphibiaweb.org/cgi/amphib_query?where-genus=Lithodytes&where-species=lineatus
  • Cintra, C. E. D., H. L. R. da Silva, and N. J. da Silva, Jr. 2014. First record of Lithodytes lineatus (Schneider, 1799) (Anura: Leptodactylidae) in the state of Tocantins, ecotone zone Amazon-Cerrado biomes, with notes on its natural history. Herpetology Notes 7: 179-184.
  • La Marca, E., C. Azevedo-Ramos, L.A. Coloma, S. Ron, J. Hardy 2010. Leptodactylus lineatus. The IUCN Red List of Threatened Species. Version 2015.2. Retrieved July 10, 2015 from http://www.iucnredlist.org/details/57177/0.
  • Schlüter, A., Löttker, P., and Mebert, K. 2009. Use of an active nest of the leaf cutter ant Atta cephalotes (Hymenoptera: Formicidae) as a breeding site of Lithodytes lineatus (Anura: Leptodactylidae). Herpetology Notes, 2, 101-105.

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Lithodytes ( Inglês )

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Lithodytes is a genus of frogs in the family of Leptodactylidae. It is monotypic, being represented by the single species, Lithodytes lineatus, also commonly known as the gold-striped frog[1] or painted antnest frog.[3] It is found in tropical South America[4] where it lives in humid forests among the leaf litter. These frogs build foam nests at the edge of temporary pools, and the tadpoles develop within these. The frogs also associate with certain leafcutter ants (Atta cephalotes) and breed inside their nests without being attacked by the ants.[5]

Description

The female Lithodytes lineatus grows to a length ranging from 38 and 52 mm (1.5 and 2.0 in), and the male is slightly smaller. It has a slender body and blunt snout. The overall color is black apart from a pair of yellow lateral stripes running from the snout to the groin, where there is a red or orange patch. The limbs are brown banded with black.[6]

This frog is similar in appearance to the brilliant-thighed poison frog (Allobates femoralis), Ameerega hahneli,[7] and the Amazonian poison-dart frog Ameerega picta.[8] By mimicking the appearance of the toxic species, Lithodytes lineatus avoids detection by predators.[6]

Development

Tadpoles of this species are bright pink in color, with the color intensity dimming near the tail. They possess translucent pink fins and dark eyes. A distinct white stripe runs down the middle of the back. Tadpoles remain in compact clusters when swimming. The distal half of the tail moves up and down rapidly to propel the tadpole forward. The presence of keratin jaws is inconsistent, and the anatomy of tooth rows also varies considerably.[9]

Distribution and habitat

Lithodytes lineatus is native to tropical South America. Its range includes the Orinoco basin and the Amazon basin and it presents in Colombia, Venezuela, the Guianas, Ecuador, Peru, Bolivia and Brazil, reaches as far as the state of Tocantins.[10] Its natural habitats are subtropical or tropical moist lowland forests, moist savanna, and intermittent freshwater marshes from altitudes ranging from sea level to 1,800 m (5,900 ft) above sea level. The species can be found below logs, among leaf-litter and in other concealed locations on the forest floor.[1]

Conservation

This common species of frog has a very wide distribution and is estimated to have a large total population. Its population may be in slight decline because of habitat degradation, but the frog seems to be able to adapt to secondary habitats. It is also present in a number of protected areas, so the International Union for Conservation of Nature (IUCN) has rated its conservation status as being of "least concern".[1]

Phylogeny

Close relatives

The genus Lithodytes is one of three subfamilies under the family Leptodactylidae, the two other subfamilies being Leiuperinae and Paratelmatobiinae. The Leptodactylidae family contains 223 total species as of 2020. Lithodytes are a distinct genus due to differences in larvae, adult morphology, and mitochondria.[8] There are also differentiating factors that distinguish the tadpoles of Lithodytes from other genera of the same family. This includes presence of labial tooth rows, unique papillae, differently shaped choanae, a long muscular tail, terminal oral disc position, and girthier trabeculae carneae.[7]

Distinct Features

Two distinct sperm types have been observed in Leptodactylidae frogs. Type I sperm has triangle-shaped head and discrete acrosome vesicles, while type II sperm has elongated head and clear acrosome vesicles. Lithodytes lineatus have type II sperm.[11] These sperm types likely evolved independently and are not connected to phylogeny, since some species have been observed to possess both types.[11] It is notable that the Lineatus have the longest sperm length of all species in the Leptodactylidae family. Males of this species also have relatively larger testes than others, indicating another distinguishing feature.[12]

Ecology and Mutualism

Lithodytes lineatus breeds in temporary pools, building foam nests in which the female lays 100 to 300 eggs. She then guards the developing eggs until the emerging tadpoles hatch.[6]

This frog is often found in association with the leaf-cutter ant, Atta cephalotes. Male Lithodytes lineatus has been observed calling from the interior of an active ants nest, seemingly unharmed by the ants.[6] The ants usually kill intruders in the nest, however it was found that the frogs captured at the entrance to the nest had a noticeable aromatic odor; researchers hypothesize that it is this odor that signals and prevents attack by the ants. In one instance, four male frogs were calling synchronously from the inside of a large ant nest, the call being a series of brief whistles at the rate of about 85 per minute.[6] Examination of another nest showed various passages and a wide vertical tunnel inside descending to the water table, with foam nests attached to roots in the wall of the tunnel and tadpoles at various stages of development in the underground pool. Ants were also moving along these tunnels.[6]

The frogs benefit from this association in that they have a well-protected breeding site and are safe from predation. The eggs of Lithodytes lineatus require protection from predatory animals such as spiders, beetles, wasps, snakes, and turtles that prey on terrestrial eggs. Additionally, ant nests provide a stable microenvironment of higher humidity than other environments, which is thought to be essential for reproduction and is optimal for frog egg development.[13] It is not clear whether the ants benefit from the arrangement, but an examination of the contents of two frogs' stomachs showed that their diet included earthworms, crickets, isopods and insect larvae, with less than 10% being ants.[14] The consumption of ants may be of benefit to ants and be tolerated by the species as it acts as a form of population control for the ants. Another possibility could be that these frogs are consuming competitors, enemies, and predatory insects of Atta cephalotes, thus decreasing competition and potentially benefiting the ants. Atta ants mainly feed on fungal symbionts growing within their nests and do not require other prey, so consumption of frog eggs in this inter-genus association is not a concern.[13][14]

Male frogs of this species have been observed calling at the entrance to, as well as from the inside of, an Atta laevigata nest. Juvenile frogs have been observed emerging from a nest of Atta sexdens.[3]

Lithodytes lineatus

Parental Care

The exact mechanism by which Lithodytes lineatus constructs foam nests remains unknown. However, studies of foam nest construction by other Leptodactylidae frogs may offer some insight into the construction process. There are a variety of ways foam nests can be made, but the most common seem to start with the male and female in an amplexus mating position, with the male on top of the female and grasping it with his front legs.[15] The pair rock back and forth, and the female discharges fertilized eggs and jelly. The male moves its legs in a motion resembling a windshield wiper, mixing air into the jelly to create foam around the fertilized eggs. This complete process takes around 4–5 seconds.[15]

The foam nests of Lithodytes lineatus are found in dry areas or seasonally wet environments of high temperature and fluctuating water levels.[16] It has been theorized that the foam prevents eggs from drying up, a disastrous result for the eggs.[17] Additionally, foam nests provide a thermal environment of elevated temperature and moisture, which allow eggs and larvae to develop rapidly. The structure of foam nests allows rapid warming and slowed heat loss.[18] The female frog stays in the center of the foam nest and guards against predators.

Studies on the composition of foam nests created by Leptodacylus vastus, a frog of the same family as Lithodytes lineatus, may lend some knowledge towards the chemical makeup of Leptodactylidae foam nests, which is still largely poorly understood. The general composition consists of a layer of surfactant proteins and a carbohydrate layer.[19] The surfactant proteins are theorized to have both hydrophilic and hydrophobic domains located at the air-water interface, allowing the formation of foam. It is assumed that these proteins must also be soluble, catalytically efficient, and non-toxic to biological tissues. Lv-RSN-1 is a notable surfactant protein since it was found to make up around 45% of the total protein composition.[19] Assays performed on this protein revealed that the presence of multiple disulfide bridges in its structure conveys high stability. This also explains resistance to heat denaturation. Along with other proteins in the nest, Lv-RSN-1 offers protection against heat and UV radiation.[19]

The foamy consistency of the nest deters a variety of predators. Snakes cannot easily swallow the nest, mammals, on the other hand, pay little attention, and insects such as ants, wasps, and beetles often become trapped in the foam and die.[17]

Social Behavior

Reproductive Behavior

Male frogs in competition have been observed to face each other when calling for mates. Their snouts oppose and almost touch each other. Males can hold this position, in the same location, for 7 consecutive nights.[12] These male frogs call in a rapid and alternating manner, generating a two-note call. The persistence of callings while facing each other suggest strong competition for mates as well as competition among males themselves. Such behavior continues without disturbance, even in the presence of close observation by humans and flashlights.[12]

Lithodytes lineatus breed during the rainy season, with pregnant females and calling males most frequently found during this time and juvenile frogs captured mostly towards the end of the season.[12] Like other species, this behavior is probably due to the requirement for standing water for development of frog larvae. It is notable that larger females lay more eggs than their smaller counterparts.[12]

Mating adults are most commonly found on the forest floor calling in close proximity to Atta nests. Large ant nests usually have multiple calling frogs.[9]

Defensive Behavior

This species employs deimatic behavior as a defense strategy.[12] During this defense, the head is lowered and rear lifted by vertical stretching of the legs. This defensive position protects the head from attack and exposes the aposematic colors of the inner thighs to potential predators. The nictitating membrane of eyes is also closed for protection during such deimatic behavior.[10]

The frog produces short and high-pitched calls when captured by predators and in distress. They also emit foamy, viscous skin secretions that have a strong bitter smell under stressful conditions.[8]

Researchers have shown that the ability of L. lineatus to safely exist in leaf-cutting Atta ant nests is connected to a biochemical compounds present in the skin of L. lineatus.[20] The exact chemical responsible for such protection against ants has yet to be determined, but this chemical produces a distinct odor.[20] Species closely related to Lithodytes lineatus (Adenomera, Allobates femoralis, and Ameerega picta) are heavily attacked by leafcutter ants while Lineatus frogs are unaffected.[20] When coated with Lineatus skin extracts, Rhinella major frogs are significantly protected from ant attack.[20] There is no observable difference between male and female skin extracts, suggesting that both sexes secrete the compound required to prevent attack by leafcutter ants.[20]

This phenomenon is not specific to L. lineatus as similar observations have been recorded in Phrynomantis microps, the West-African savanna frog, and Paltothyreus tarsatus, commonly known as Ponerine ants.[21] Recent studies have identified potential amino acids responsible for the lack of attack by these Ponerine ants.[21] These peptides were similarly studied as those in L. lineatus and when skin extract from P. microps was used to coat termites, the ants would no longer attack these termites.[21] Thus, similar resistance against ant attack was conferred through the skin extracts of these frogs. Researchers hypothesize that these peptides act as "appeasement allomones" and have potential applications in the reduction of insect aggression.[21]

Foraging Behavior

Adults usually hunt at night and are sometimes found away from shelter and residence, typically for the purpose of foraging.[9]

Protective Coloration and Behavior

Batesian mimicry

Lithodytes lineatus has been considered non-toxic and its morphological similarity to the poison dart frog Ameerega picta has resulted in conclusions of Batesian mimicry between the two organisms. However, studies of the skin and poison glands of L. lineatus revealed a limited diversity of proteins and peptides that potentially have toxic effects.[8] Comparisons of skin and glands between L. lineatus and A. picta show differences in gland shape, distribution, concentration, and in type of granule secreted. The poison of A. picta, unlike that of L. lineatus, contains no proteins and is instead composed of alkaloids and carbohydrates.[8]

Furthermore, the poison glands of L. lineatus are concentrated in the head and colored bands of the dorsum (yellow stripes and orange spots).[8] This localization of poison glands in L. lineatus is unlike A. picta and most anurans, which possess a homogenous distribution of glands.[8] Such localized distribution signals to predators that poison is actually located at the colored stripes and spots. A high concentration of glands on the head is theorized to be a result of frog predators starting consumption of anurans at the head.[17]

Müllerian mimicry

The recent finding of potentially poisonous characteristics in L. lineatus has resulted in a re-definition of the association between this species and A. picta. Predators could learn to avoid the shared color patterns between these two species, resulting in Müllerian mimicry.[8]

Use in Research

Analysis of anuran skin secretion chemical composition is important and is commonly done because substances found in such secretions can potentially serve as antimicrobials.[22] Benzocaine, a local anesthetic, is frequently orally administered in lethal dosages to humanely kill anurans for study. However, the use of this anesthetic was temporarily a cause for concern in 2018 due to the finding of benzocaine in the skin extracts of the species Melanophryniscus moreirae and Lithobates clamitans, potentially invalidating many compositional studies of skin extracts. Fortunately, it was confirmed in 2020 that orally administered gel benzocaine did not result in the detection of any benzocaine in the skin of Lithodytes lineatus.[22] Benzocaine in liquid form could result in false positives, but benzocaine in gel form applied at toxic doses in the mouths of frogs does not impact the chemical compositions of frog skin extracts and also should not confound any assays done with skin extracts.[22]

References

  1. ^ a b c d Enrique La Marca, Claudia Azevedo-Ramos, Luis A. Coloma, Santiago Ron, Jerry Hardy (2010). "Lithodytes lineatus". IUCN Red List of Threatened Species. 2010: e.T57177A11580398. doi:10.2305/IUCN.UK.2010-2.RLTS.T57177A11580398.en. Retrieved 15 November 2021.{{cite journal}}: CS1 maint: multiple names: authors list (link)
  2. ^ Frost, Darrel R. (2020). "Lithodytes lineatus (Schneider, 1799)". Amphibian Species of the World: An Online Reference. Version 6.1. American Museum of Natural History. doi:10.5531/db.vz.0001. Retrieved 28 May 2020.
  3. ^ a b Barros, Andre; Lozano, Jorge Luis Lopez; Lima, Albertina (2016). "Lithodytes lineatus (painted antnest frog) association with Atta ants". Herpetological Review. 47 (4): 643.
  4. ^ Frost, Darrel R. (2020). "Lithodytes Fitzinger, 1843". Amphibian Species of the World: An Online Reference. Version 6.1. American Museum of Natural History. doi:10.5531/db.vz.0001. Retrieved 28 May 2020.
  5. ^ "Amazonian frog has its own ant repellent". ScienceDaily. 2 October 2016. Retrieved 2 June 2020.
  6. ^ a b c d e f Halliday, Tim (2016). The Book of Frogs: A Life-Size Guide to Six Hundred Species from Around the World. University of Chicago Press. p. 244. ISBN 978-0-226-18465-4.
  7. ^ a b Nascimento, Filipe A. C. do; de Sá, Rafael O.; Garcia, Paulo C. de A. (2021-01-01). "Larval anatomy of monotypic painted ant nest frogs Lithodytes lineatus reveals putative homoplasies with the Leptodactylus pentadactylus group (Anura: Leptodactylidae)". Zoologischer Anzeiger. 290: 135–147. doi:10.1016/j.jcz.2020.12.003. ISSN 0044-5231. S2CID 234171975.
  8. ^ a b c d e f g h Prates, Ivan; Antoniazzi, Marta M.; Sciani, Juliana M.; Pimenta, Daniel C.; Toledo, Luís Felipe; Haddad, Célio F.B.; Jared, Carlos (2012). "Skin glands, poison and mimicry in dendrobatid and leptodactylid amphibians". Journal of Morphology. 273 (3): 279–290. doi:10.1002/jmor.11021. PMID 22025347. S2CID 6193152.
  9. ^ a b c Lamar, William W., and E. R. Wild. "Comments on the natural history of Lithodytes lineatus (Anura: Leptodactylidae), with a description of the tadpole." Herpetological Natural History 3, no. 2 (1995): 135-142.
  10. ^ a b Cintra, Carlos Eduardo Domingos. “First Record of Lithodytes Lineatus (Schneider, 1799) (Anura: Leptodactylidae) in the State of Tocantins, Ecotone Zone Amazon-Cerrado Biomes, with Notes on Its Natural History,” n.d., 7.
  11. ^ a b Salles, Natália M. E.; Zara, Fernando J.; Prado, Cynthia P. A. (2017). "Differences in sperm morphology in foam-nesting leptodactyline frogs (Anura, Leptodactylidae)". Acta Zoologica. 98: 1–12. doi:10.1111/azo.12144.
  12. ^ a b c d e f Bernarde, Paulo Sérgio; Kokubum, Marcelo N. de C. (2009). "Seasonality, age structure and reproduction of Leptodactylus (Lithodytes) lineatus (Anura, Leptodactylidae) in Rondônia state, southwestern Amazon, Brazil". Iheringia. Série Zoologia. 99 (4): 368–372. doi:10.1590/S0073-47212009000400005.
  13. ^ a b Barros, André de Lima. “INSTITUTO NACIONAL DE PESQUISAS DA AMAZÔNIA - INPA PROGRAMA DE PÓS-GRADUAÇÃO EM ECOLOGIA,” 2016, 36.
  14. ^ a b Schlüter, Andreas; Löttker, Petra & Mebe, Konrad (2009). "Use of an active nest of the leaf cutter ant Atta cephalotes (Hymenoptera: Formicidae) as a breeding site of Lithodytes lineatus (Anura: Leptodactylidae)". Herpetology Notes. 2: 101–105.
  15. ^ a b Heyer, W. Ronald, and A. Stanley Rand. "Foam nest construction in the leptodactylid frogs Leptodactylus pentadactylus and Physalaemus pustulosus (Amphibia, Anura, Leptodactylidae)." Journal of Herpetology 11, no. 2 (1977): 225-228.
  16. ^ Crump, Martha L. (2015). "Anuran Reproductive Modes: Evolving Perspectives". Journal of Herpetology. 49: 1–16. doi:10.1670/14-097. S2CID 85751247.
  17. ^ a b c Villa, Jaime, Roy W McDiarmid, and José M Gallardo. “ARTHROPOD PREDATORS OF LEPTODACTYLID FROG FOAM NESTS,” n.d., 14.
  18. ^ Dobkin, David S.; Gettinger, Ronald D. (1985). "Thermal Aspects of Anuran Foam Nests". Journal of Herpetology. 19 (2): 271–275. doi:10.2307/1564181. JSTOR 1564181.
  19. ^ a b c Hissa, Denise Cavalcante; Bezerra, Walderly Melgaço; Freitas, Cléverson Diniz Teixeira De; Ramos, Márcio Viana; Lopes, José Luiz De Souza; Beltramini, Leila Maria; Roberto, Igor Joventino; Cascon, Paulo; Melo, Vânia Maria Maciel (2016). "Frog Foam Nest Protein Diversity and Synthesis". Journal of Experimental Zoology Part A: Ecological Genetics and Physiology. 325 (7): 425–433. doi:10.1002/jez.2027. PMID 27460953.
  20. ^ a b c d e de Lima Barros, André; López-Lozano, Jorge Luis; Lima, Albertina Pimentel (2016-10-20). "The frog Lithodytes lineatus (Anura: Leptodactylidae) uses chemical recognition to live in colonies of leaf-cutting ants of the genus Atta (Hymenoptera: Formicidae)". Behavioral Ecology and Sociobiology. 70 (12): 2195–2201. doi:10.1007/s00265-016-2223-y. ISSN 0340-5443. S2CID 253815151.
  21. ^ a b c d Rödel, Mark-Oliver; Brede, Christian; Hirschfeld, Mareike; Schmitt, Thomas; Favreau, Philippe; Stöcklin, Reto; Wunder, Cora; Mebs, Dietrich (2013). "Chemical camouflage--a frog's strategy to co-exist with aggressive ants". PLOS ONE. 8 (12): e81950. Bibcode:2013PLoSO...881950R. doi:10.1371/journal.pone.0081950. ISSN 1932-6203. PMC 3859521. PMID 24349157.
  22. ^ a b c Barros, André de Lima; Lima, Albertina Pimentel; Fachin-Espinar, Maria Teresa; Nunez, Cecilia Veronica (2020). "Evaluation of benzocaine-based anesthetic gel in anuran skins extracts: A case study using the frog Lithodytes lineatus (Anura: Leptodactylidae)". PLOS ONE. 15 (12): e0243654. Bibcode:2020PLoSO..1543654B. doi:10.1371/journal.pone.0243654. PMC 7723253. PMID 33290419.

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Lithodytes: Brief Summary ( Inglês )

fornecido por wikipedia EN

Lithodytes is a genus of frogs in the family of Leptodactylidae. It is monotypic, being represented by the single species, Lithodytes lineatus, also commonly known as the gold-striped frog or painted antnest frog. It is found in tropical South America where it lives in humid forests among the leaf litter. These frogs build foam nests at the edge of temporary pools, and the tadpoles develop within these. The frogs also associate with certain leafcutter ants (Atta cephalotes) and breed inside their nests without being attacked by the ants.

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Lithodytes lineatus ( Espanhol; Castelhano )

fornecido por wikipedia ES

Lithodytes lineatus es una especie de anfibio anuro de la familia Leptodactylidae y única representante del género Lithodytes. Se encuentra en Bolivia, Brasil, Colombia, Ecuador, Guayana francesa, Guayana, Perú, Surinam, Venezuela, y posiblemente la isla Trinidad.

Referencias

  • Frost, D.R. «Lithodytes lineatus ». Amphibian Species of the World: an Online Reference. Version 6.1. (en inglés). Nueva York, EEUU: Museo Americano de Historia Natural. Consultado el 8 de junio de 2015.

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Lithodytes lineatus: Brief Summary ( Espanhol; Castelhano )

fornecido por wikipedia ES

Lithodytes lineatus es una especie de anfibio anuro de la familia Leptodactylidae y única representante del género Lithodytes. Se encuentra en Bolivia, Brasil, Colombia, Ecuador, Guayana francesa, Guayana, Perú, Surinam, Venezuela, y posiblemente la isla Trinidad.

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Leptodactylus lineatus ( Basco )

fornecido por wikipedia EU

Leptodactylus lineatus Leptodactylus generoko animalia da. Anfibioen barruko Leptodactylidae familian sailkatuta dago, Anura ordenan.

Erreferentziak

Ikus, gainera

(RLQ=window.RLQ||[]).push(function(){mw.log.warn("Gadget "ErrefAurrebista" was not loaded. Please migrate it to use ResourceLoader. See u003Chttps://eu.wikipedia.org/wiki/Berezi:Gadgetaku003E.");});
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Leptodactylus lineatus: Brief Summary ( Basco )

fornecido por wikipedia EU

Leptodactylus lineatus Leptodactylus generoko animalia da. Anfibioen barruko Leptodactylidae familian sailkatuta dago, Anura ordenan.

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Lithodytes lineatus ( Francês )

fornecido por wikipedia FR

Lithodytes lineatus, unique représentant du genre Lithodytes, est une espèce d'amphibiens de la famille des Leptodactylidae[1].

Répartition

Cette espèce se rencontre du niveau de la mer jusqu'à 1 800 m d'altitude dans l'est du Pérou, dans l'est de l'Équateur, en Bolivie, au Brésil, au Venezuela, en Guyane, au Guyana et au Suriname[1],[2].

Lithodytes lineatus.jpg

Publications originales

  • Fitzinger, 1843 : Systema Reptilium, fasciculus primus, Amblyglossae. Braumüller et Seidel, Wien, p. 1-106 (texte intégral).
  • Schneider, 1799 : Historiae amphibiorum naturalis et literariae fasciculus primus, vol. 1 (texte intégral).

Notes et références

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Lithodytes lineatus: Brief Summary ( Francês )

fornecido por wikipedia FR

Lithodytes lineatus, unique représentant du genre Lithodytes, est une espèce d'amphibiens de la famille des Leptodactylidae.

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Lithodytes lineatus ( Neerlandês; Flamengo )

fornecido por wikipedia NL

Herpetologie

Lithodytes lineatus is een kikker uit de familie fluitkikkers (Leptodactylidae). Het is de enige soort uit het monotypische geslacht Lithodytes. De groep werd voor het eerst wetenschappelijk beschreven door Johann Gottlob Schneider in 1799. Oorspronkelijk werd de wetenschappelijke naam Rana lineata gebruikt.[1] De soortaanduiding lineatus betekent vrij vertaald 'gestreept'.

Uiterlijke kenmerken

De kikker bereikt een lichaamslengte van ongeveer vier tot vijf centimeter, de mannetjes blijven kleiner dan de vrouwtjes. De snuit van de kikker is afgerond, de diameter van het tympanum of trommelvlies is ongeveer gelijk aan de diameter van het oog. De lichaamskleur donkerbruin tot zwart, van de snuit tot de lies is een gele streep aanwezig aan de bovenzijde van de flank die aan de snuitpunt verbonden zijn. Op de bovenzijde van de lies is een opvallende rode vlek aanwezig.

Verspreiding en habitat

Lithodytes lineatus komt voor in delen van Zuid-Amerika en leeft in de landen Bolivia, Brazilië, Colombia, Ecuador, Frans-Guyana, Guyana, Peru, Suriname en Venezuela.[2] De kikker leeft in tropische regenwouden en is te vinden in de strooisellaag tussen de bladeren en onder stukken hout.


Referenties
  1. Darrel R. Frost - Amphibian Species of the World: an online reference - Version 6.0 - American Museum of Natural History, Lithodytes lineatus.
  2. University of California - AmphibiaWeb, Lithodytes lineatus.
Bronnen
  • (en) - Darrel R. Frost - Amphibian Species of the World: an online reference - Version 6.0 - American Museum of Natural History - Lithodytes lineatus - Website Geconsulteerd 10 januari 2017
  • (en) - University of California - AmphibiaWeb - Lithodytes lineatus - Website
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Lithodytes lineatus: Brief Summary ( Neerlandês; Flamengo )

fornecido por wikipedia NL

Lithodytes lineatus is een kikker uit de familie fluitkikkers (Leptodactylidae). Het is de enige soort uit het monotypische geslacht Lithodytes. De groep werd voor het eerst wetenschappelijk beschreven door Johann Gottlob Schneider in 1799. Oorspronkelijk werd de wetenschappelijke naam Rana lineata gebruikt. De soortaanduiding lineatus betekent vrij vertaald 'gestreept'.

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Lithodytes lineatus ( Português )

fornecido por wikipedia PT

Sapito-listado (Lithodytes lineatus) é uma espécie de da família Leptodactylidae.

Habitat

Pode ser encontrada na Bolívia, Brasil, Colômbia, Equador, Guiana Francesa, Guiana, Peru, Suriname, Venezuela e possivelmente Trinidad e Tobago. O seu habitat natural são subtropicais ou tropicais húmidas baixa altitude florestas de baixa altitude tropicais ou subtropicais húmidas: savanas húmidas e marismas de água doce temporárias variando em altitude do nível do mar até 1800 m acima do nível do mar.

A espécie pode ser encontrada debaixo de troncos, detritos vegetais e outra tpo de cobertura florestal. Constroem ninhos de espuma na beira de charcos temporárias; as larvas desenvolvem-se dentro dessas massas de água.

Referências

  1. Enrique La Marca, Claudia Azevedo-Ramos, Luis A. Coloma, Santiago Ron, Jerry Hardy (2010). «Lithodytes lineatus». Lista Vermelha de Espécies Ameaçadas. 2010: e.T57177A11580398. doi:. Consultado em 15 de novembro de 2021
  2. Frost, Darrel R. (2020). «Lithodytes lineatus (Schneider, 1799)». American Museum of Natural History. Amphibian Species of the World: An Online Reference. Version 6.1. doi:10.5531/db.vz.0001. Consultado em 28 de maio de 2020
  • Este artigo foi inicialmente traduzido, total ou parcialmente, do artigo da Wikipédia em inglês, cujo título é «Sapito Listado», especificamente .
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Lithodytes lineatus: Brief Summary ( Português )

fornecido por wikipedia PT

Sapito-listado (Lithodytes lineatus) é uma espécie de da família Leptodactylidae.

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Lithodytes lineatus ( Vietnamita )

fornecido por wikipedia VI

Lithodytes lineatus là một loài ếch trong họ Leptodactylidae. Nó là đại diện duy nhất của chi Lithodytes.

Môi trường sống

Nó được tìm thấy ở Bolivia, Brasil, Colombia, Ecuador, Guyane thuộc Pháp, Guyana, Peru, Suriname, Venezuela, và có thể cả Trinidad và Tobago. Các môi trường sống tự nhiên của chúng là các khu rừng ẩm ướt đất thấp nhiệt đới hoặc cận nhiệt đới, xavan ẩm, và đầm nước ngọt có nước theo mùa.

Hình ảnh

Chú thích

  1. ^ La Marca, E., Azevedo-Ramos, C., Coloma, L.A., Ron, S. & Hardy, J. (2010). Lithodytes lineatus. Sách Đỏ IUCN các loài bị đe dọa. Phiên bản 2013.1. Liên minh Bảo tồn Thiên nhiên Quốc tế. Truy cập ngày 4 tháng 12 năm 2013.

Tham khảo


Hình tượng sơ khai Bài viết Leptodactylidae này vẫn còn sơ khai. Bạn có thể giúp Wikipedia bằng cách mở rộng nội dung để bài được hoàn chỉnh hơn.


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Lithodytes lineatus: Brief Summary ( Vietnamita )

fornecido por wikipedia VI

Lithodytes lineatus là một loài ếch trong họ Leptodactylidae. Nó là đại diện duy nhất của chi Lithodytes.

licença
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Wikipedia tác giả và biên tập viên
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site do parceiro
wikipedia VI