Frogs are amphibians in the order Anura (meaning "tail-less", from Greek an-, without + oura, tail), formerly referred to as Salientia (Latin salere (salio), "to jump"). Most frogs are characterized by a short body, webbed digits (fingers or toes), protruding eyes and the absence of a tail. Frogs are widely known as exceptional jumpers, and many of the anatomical characteristics of frogs, particularly their long, powerful legs, are adaptations to improve jumping performance. Due to their permeable skin, frogs are often semi-aquatic or inhabit humid areas, but move easily on land. They typically lay their eggs in puddles, ponds or lakes, and their larvae, called tadpoles, have gills and develop in water. Adult frogs follow a carnivorous diet, mostly of arthropods, annelids and gastropods. Frogs are most noticeable by their call, which can be widely heard during the night or day, mainly in their mating season.
The distribution of frogs ranges from tropic to subarctic regions, but most species are found in tropical rainforests. Consisting of more than 5,000 species described, they are among the most diverse groups of vertebrates. However, populations of certain frog species are declining significantly.
A popular distinction is often made between frogs and toads on the basis of their appearance, but this has no taxonomic basis. (Members of the anuran family Bufonidae are called true toads, but many species from other families are also called toads.) In addition to their ecological importance, frogs have many cultural roles, such as in literature, symbolism and religion, and they are also valued as food and as pets.
A distinction is often made between frogs and toads on the basis of their appearance, caused by the convergent adaptation among so-called toads to dry environments; however, this distinction has no taxonomic basis. The only family exclusively given the common name "toad" is Bufonidae, but many species from other families are also called "toads," and the species within the toad genus Atelopus are referred to as "harlequin frogs".
Frogs and toads are broadly classified into three suborders: Archaeobatrachia, which includes four families of primitive frogs; Mesobatrachia, which includes five families of more evolutionary intermediate frogs; and Neobatrachia, by far the largest group, which contains the remaining 24 families of "modern" frogs, including most common species throughout the world. Neobatrachia is further divided into the Hyloidea and Ranoidea. This classification is based on such morphological features as the number of vertebrae, the structure of the pectoral girdle, and the morphology of tadpoles. While this classification is largely accepted, relationships among families of frogs are still debated. Future studies of molecular genetics should soon provide further insights to the evolutionary relationships among anuran families.
Some species of anurans hybridise readily. For instance, the Edible Frog (Rana esculenta) is a hybrid of the Pool Frog (R. lessonae) and the Marsh Frog (R. ridibunda). Bombina bombina and Bombina variegata similarly form hybrids, although these are less fertile, giving rise to a hybrid zone.
Many characteristics are not shared by all of the approximately 5,250 described frog species. However, some general characteristics distinguish them from other amphibians. Frogs are usually well suited to jumping, with long hind legs and elongated ankle bones. They have a short vertebral column, with no more than ten free vertebrae, followed by a fused tailbone (urostyle or coccyx), typically resulting in a tailless phenotype.
Frogs range in size from (Brachycephalus didactylus of Brazil and Eleutherodactylus iberia of Cuba) to (goliath frog, Conraua goliath, of Cameroon). The skin hangs loosely on the body because of the lack of loose connective tissue. Skin texture varies: it can be smooth, warty or folded. Frogs have three eyelid membranes: one is transparent to protect the eyes underwater, and two vary from translucent to opaque. Frogs have a tympanum on each side of the head, which is involved in hearing and, in some species, is covered by skin. Most frogs have teeth, specifically pedicellate teeth in which the crown is separated from the root by fibrous tissue. Most only have teeth on the edge of the upper jaw (maxillary teeth) as well as vomerine teeth on the roof of their mouth. They do not have any teeth on their lower jaw, so they usually swallow their food whole. The teeth are mainly used to hold the prey and keep it in place till they can get a good grip on it and swallow their meal, assisted by retracting their eyes into their head. True toads lack any teeth at all, and some species (Pyxicephalus) which prey on relatively large organisms (including mice and other frogs) have cone shaped projections of bone, called odontoid processes, at the front of the lower jaw which function like teeth.
The structure of the feet and legs varies greatly among frog species, depending in part on whether they live primarily on the ground, in water, in trees, or in burrows. Frogs must be able to move quickly through their environment to catch prey and escape predators, and numerous adaptations help them do so.
Many frogs, especially those that live in water, have webbed toes. The degree to which the toes are webbed is directly proportional to the amount of time the species lives in the water. For example, the completely aquatic African dwarf frog (Hymenochirus sp.) has fully webbed toes, whereas the toes of White's tree frog (Litoria caerulea), an arboreal species, are only a half or a quarter webbed.
Arboreal frogs have "toe pads" to help grip vertical surfaces. These pads, located on the ends of the toes, do not work by suction. Rather, the surface of the pad consists of interlocking cells, with a small gap between adjacent cells. When the frog applies pressure to the toe pads, the interlocking cells grip irregularities on the substrate. The small gaps between the cells drain away all but a thin layer of moisture on the pad, and maintain a grip through capillarity. This allows the frog to grip smooth surfaces, and does not function when the pads are excessively wet.
In many arboreal frogs, a small "intercalary structure" in each toe increases the surface area touching the substrate. Furthermore, since hopping through trees can be dangerous, many arboreal frogs have hip joints that allow both hopping and walking. Some frogs that live high in trees even possess an elaborate degree of webbing between their toes, as do aquatic frogs. In these arboreal frogs, the webs allow the frogs to "parachute" or control their glide from one position in the canopy to another.
Ground-dwelling frogs generally lack the adaptations of aquatic and arboreal frogs. Most have smaller toe pads, if any, and little webbing. Some burrowing frogs have a toe extension—a metatarsal tubercle—that helps them to burrow. The hind legs of ground dwellers are more muscular than those of aqueous and tree-dwelling frogs.
Sometimes during the tadpole stage, one of the animal's rear leg stubs is eaten by a dragonfly nymph. In some of these cases, the full leg grows anyway, and in other cases, it does not, although the frog may still live out its normal lifespan with only three legs. Other times, a parasitic flatworm called Riberoria trematodes digs into the rear of a tadpole, where it rearranges the limb bud cells, which sometimes causes the frog to have extra legs.
While frog species can use a variety of locomotor modes (running, walking, gliding, swimming, and climbing), more are either proficient at jumping or descended from ancestors who were, with much of the musculo-skeletal morphology modified for this purpose. The tibia, fibula and tarsals have been fused into a single, strong bone, as have the radius and ulna in the forelimbs (which must absorb the impact of landing). The metatarsals have become elongated to add to the leg length and allow the frog to push against the ground for longer during a jump. The illium has elongated and formed a mobile joint with the sacrum which, in specialist jumpers such as Ranids or Hylids, functions as an additional limb joint to further power the leaps. This elongation of the limbs results in the frog being able to apply force to the ground for longer during a jump, which in turn results in a longer, faster jump.
The muscular system has been similarly modified. The hind limbs of the ancestor of frogs presumably contained pairs of muscles which would act in opposition (one muscle to flex the knee, a different muscle to extend it), as is seen in most other limbed animals. However, in modern frogs, almost all muscles have been modified to contribute to the action of jumping, with only a few small muscles remaining to bring the limb back to the starting position and maintain posture. The muscles have also been greatly enlarged, with the muscles involved in jumping accounting for over 17% of the total mass of the frog.
In some extremely capable jumpers, such as the cuban tree frog, the peak power exerted during a jump can exceed what muscle is capable of producing. Currently, it is hypothesized that frogs are storing muscular energy by stretching their tendons like springs, then triggering the release all at once, allowing the frog to increase the energy of its jump beyond the limits of muscle-powered acceleration. A similar mechanism has already been documented in locusts and grasshoppers.
Many frogs are able to absorb water and oxygen directly through the skin, especially around the pelvic area. However, the permeability of a frog's skin can also result in water loss. Some tree frogs reduce water loss with a waterproof layer of skin. Others have adapted behaviours to conserve water, including engaging in nocturnal activity and resting in a water-conserving position. This position involves the frog lying with its toes and fingers tucked under its body and chin, respectively, with no gap between the body and substrate. Some frog species will also rest in large groups, touching the skin of the neighbouring frog. This reduces the amount of skin exposed to the air or a dry surface, and thus reduces water loss. These adaptations only reduce water loss enough for a predominantly arboreal existence, and are not suitable for arid conditions.
Camouflage is a common defensive mechanism in frogs. Most camouflaged frogs are nocturnal, which adds to their ability to hide. Nocturnal frogs usually find the ideal camouflaged position during the day to sleep. Some frogs have the ability to change colour, but this is usually restricted to shades of one or two colours. For example, White's tree frog varies in shades of green and brown. Features such as warts and skin folds are usually found on ground-dwelling frogs, where a smooth skin would not disguise them effectively. Arboreal frogs usually have smooth skin, enabling them to disguise themselves as leaves.
Certain frogs change colour between night and day, as light and moisture stimulate the pigment cells and cause them to expand or contract.
Some frogs obtain poisons from the ants and other arthropods they eat; others, such as the Australian Corroboree Frogs (Pseudophryne corroboree and Pseudophryne pengilleyi), can manufacture an alkaloid not derived from their diet. Some native people of South America extract poison from the poison dart frogs and apply it to their darts for hunting, although few species are toxic enough to be used for this purpose. It was previously a misconception the poison was placed on arrows rather than darts. The common name of these frogs was thus changed from "poison arrow frog" to "poison dart frog" in the early 1980s. Poisonous frogs tend to advertise their toxicity with bright colours, an adaptive strategy known as aposematism. There are at least two non-poisonous species of frogs in tropical America (Eleutherodactylus gaigei and Lithodytes lineatus) that mimic the colouration of dart poison frogs' coloration for self-protection (Batesian mimicry).
Because frog toxins are extraordinarily diverse, they have raised the interest of biochemists as a "natural pharmacy". The alkaloid epibatidine, a painkiller 200 times more potent than morphine, is found in some species of poison dart frogs. Other chemicals isolated from the skin of frogs may offer resistance to HIV infection. Arrow and dart poisons are under active investigation for their potential as therapeutic drugs.
The skin secretions of some toads, such as the Colorado River toad and cane toad, contain bufotoxins, some of which, such as bufotenin, are psychoactive, and have therefore been used as recreational drugs. Typically, the skin secretions are dried and smoked. Skin licking is especially dangerous, and appears to constitute an urban myth. See psychoactive toad.
Frogs are known for their three-chambered heart, which they share with all tetrapods except birds, crocodilians and mammals. In the three-chambered heart, oxygenated blood from the lungs and de-oxygenated blood from the respiring tissues enter by separate atria, and are directed via a spiral valve to the appropriate vessel—aorta for oxygenated blood and pulmonary artery for deoxygenated blood. This special structure is essential to keeping the mixing of the two types of blood to a minimum, which enables frogs to have higher metabolic rates, and to be more active than otherwise.
Some species of frog have remarkable adaptations that allow them to survive in oxygen deficient water. The lake titicaca frog (Telmatobius culeus) is one such species and to survive in the poorly oxygenated waters of Lake Titicaca it has incredibly wrinkly skin that increases its surface area to enhance gas exchange. This frog will also do 'push-ups' on the lake bed to increase the flow of water around its body.
Eggs hatch and continue life as tadpoles (occasionally known as polliwogs), which typically have oval bodies and long, vertically flattened tails. At least one species (Nannophrys ceylonensis) has tadpoles that are semi-terrestrial and live among wet rocks, but as a general rule, free living larvae are fully aquatic. They lack eyelids and have a cartilaginous skeleton, a lateral line system, gills for respiration (external gills at first, internal gills later) and tails with dorsal and ventral folds of skin for swimming. From pretty early onward they develop a gill pouch that covers the gills and the front legs and also the lungs are developed in an early stage as an accessory breathing organ. Some species which go through the metamorphosis inside the egg and hatch to small frogs never develop gills, instead there are specialised areas of skin that takes care of the respiration. Tadpoles also lack true teeth, but the jaws in most species usually have two elongate, parallel rows of small keratinized structures called keradonts in the upper jaw while the lower jaw has three rows of keradonts, surrounded by a horny beak, but the number of rows can be lower or absent, or much higher. Tadpoles are typically herbivorous, feeding mostly on algae, including diatoms filtered from the water through the gills. Some species are carnivorous at the tadpole stage, eating insects, smaller tadpoles, and fish. Cannibalism has been observed among tadpoles. Early developers who gain legs may be eaten by the others, so the late bloomers survive longer. This has been observed in England in the species Rana temporaria (common frog).
Tadpoles are highly vulnerable to predation by fish, newts, predatory diving beetles and birds such as kingfishers. Poisonous tadpoles are present in many species, such as Cane Toads. The tadpole stage may be as short as a week, or tadpoles may overwinter and metamorphose the following year in some species, such as the midwife toad (Alytes obstetricans) and the common spadefoot (Pelobates fuscus). In the Pipidae, with the exception for Hymenochirus, the tadpoles have paired anterior barbels which make them resemble small catfish.
With the exception of the base of the tail, where a few vertebral structures develop to give rise to the urostyle later in life, the tail lacks the completely solid, segmental, skeletal elements of cartilage or bony tissue that are so typical for other vertebrates, although it does contain a notochord
At the end of the tadpole stage, frogs undergo metamorphosis, in which they undergo a transition into the adult form. This metamorphosis last typically only 24 hours and consists of:
Frogs and toads can live for many years; though little is known about their life span in the wild, captive frogs and toads are recorded living up to 40 years.
Frogs from temperate climates hibernate through the winter, and 4 species are known to freeze during this time, most notably Rana sylvatica.
Once at the breeding ground, male frogs call to attract a mate, collectively becoming a chorus of frogs. The call is unique to the species, and will attract females of that species. Some species have satellite males who do not call, but intercept females that are approaching a calling male.
The male and female frogs then undergo amplexus. This involves the male mounting the female and gripping her (sometimes with special nuptial pads) tightly. Fertilization is external: the egg and sperm meet outside of the body. The female releases her eggs, which the male frog covers with a sperm solution. The eggs then swell and develop a protective coating. The eggs are typically brown or black, with a clear, gelatin-like covering.
Most temperate species of frogs reproduce between late autumn and early spring. In the UK, most common frog populations produce frogspawn in February, although there is wide variation in timing. Water temperatures at this time of year are relatively low, typically between four and 10 degrees Celsius. Reproducing in these conditions helps the developing tadpoles because dissolved oxygen concentrations in the water are highest at cold temperatures. More importantly, reproducing early in the season ensures that appropriate food is available to the developing frogs at the right time.
The evolution of parental care in frogs is driven primarily by the size of the water body in which they breed. There is an inverse relationship between the level of parental care in a frog species and the degree of parental care they exhibit—frogs that breed in smaller water bodies tend to have more complex parental care behaviors. Water body size shows this strong relationship with parental care because it encompasses several important variables that interact to select for parental care: predation, desiccation, competition, and resource limitation. Because predation of eggs and larvae is high in large water bodies, a number of frog species evolved terrestrial oviposition. Once eggs are deposited on land, the desiccating terrestrial environment demands uniparental care in the form of egg hydration to ensure egg survival. The subsequent need to transport hatched tadpoles to a water source requires an even more intense form of uniparental care. In small water bodies where predators are mostly absent, such as phytotelmata (water-filled leaf axils or small woody cavities), inter-tadpole competition becomes the variable that constrains tadpole survival. Certain frogs species avoid this competition by evolving the use of smaller phytotelmata as tadpole deposition sites. However, while these smaller tadpole rearing sites are free of competition, they also lack nutrients. Because they do not have sufficient nutrients to support a tadpole without parental provisioning behavior, frog species that transitioned from the use of larger to smaller phytotelmata have evolved trophic (unfertilized) egg laying. In this complex form of biparental care, the female provides her offspring with nutritive eggs. While each of these variables select for different behaviors, they correlate with the size of a species' tadpole-rearing site and influence the degree of parental care displayed by a species.
Some frogs lack vocal sacs, such as those from the genera Heleioporus and Neobatrachus, but these species can still produce a loud call. Their buccal cavity is enlarged and dome-shaped, acting as a resonance chamber that amplifies their call. Species of frog without vocal sacs and that do not have a loud call tend to inhabit areas close to flowing water. The noise of flowing water overpowers any call, so they must communicate by other means.
The main reason for calling is to allow males to attract a mate. Males call either individually or in a group called a chorus. Females of many frog species, for example Polypedates leucomystax, produce calls reciprocal to the males', which act as the catalyst for the enhancement of reproductive activity in a breeding colony. A male frog emits a release call when mounted by another male. Tropical species also have a rain call that they make on the basis of humidity cues prior to a rain shower. Many species also have a territorial call that is used to chase away other males. All of these calls are emitted with the mouth of the frog closed.
A distress call, emitted by some frogs when they are in danger, is produced with the mouth open, resulting in a higher-pitched call. The effectiveness of the call is unknown; however, it is suspected the call intrigues the predator until another animal is attracted, distracting them enough for its escape.
Many species of frog have deep calls, or croaks. The English onomatopoeic spelling is "ribbit". The croak of the American bullfrog (Rana catesbiana) is sometimes spelt "jug o' rum". Other examples are Ancient Greek brekekekex koax koax for probably Rana ridibunda, and the description in Rigveda 7:103.6 gómāyur éko ajámāyur ékaħ = "one has a voice like a cow's, one has a voice like a goat's".
A Canadian study conducted in 2006, suggested heavy traffic near frog habitats as a large threat to frog populations. In a few cases, captive breeding programs have been attempted to alleviate the pressure on frog populations, and these have proved successful. In 2007, it was reported the application of certain probiotic bacteria could protect amphibians from chytridiomycosis. One current project, The Panama Amphibian Rescue and Conservation Project, has subsequently been developed in order to rescue species at risk of chytridiomycosis in eastern Panama, and to develop field applications of this probiotic cure.
Zoos and aquariums around the world named 2008 the Year of the Frog, to draw attention to the conservation issues.
Until the discovery of the Early Permian Gerobatrachus hottoni in 2008, a stem-batrachian with many salamander-like characteristics, the earliest known proto-frog was Triadobatrachus massinoti, from the 250 million year old early Triassic of Madagascar. The skull is frog-like, being broad with large eye sockets, but the fossil has features diverging from modern amphibia. These include a different ilium, a longer body with more vertebrae, and separate vertebrae in its tail (whereas in modern frogs, the tail vertebrae are fused, and known as the urostyle or coccyx). The tibia and fibula bones are unfused and separate, making it probable Triadobatrachus was not an efficient leaper.
Another fossil frog, Prosalirus bitis, was discovered in 1995. The remains were recovered from Arizona's Kayenta Formation, which dates back to the Early Jurassic epoch, somewhat younger than Triadobatrachus. Like Triadobatrachus, Prosalirus did not have greatly enlarged legs, but had the typical three-pronged pelvic structure. Unlike Triadobatrachus, Prosalirus had already lost nearly all of its tail and was well adapted for jumping.
The earliest known "true frog" is Vieraella herbsti, from the early Jurassic (188–213 million years ago). It is known only from the dorsal and ventral impressions of a single animal and was estimated to be from snout to vent. Notobatrachus degiustoi from the middle Jurassic is slightly younger, about 155–170 million years old. It is likely the evolution of modern Anura was completed by the Jurassic period. The main evolutionary changes involved the shortening of the body and the loss of the tail.
The earliest full fossil record of a modern frog is of sanyanlichan, which lived 125 million years ago and had all modern frog features, but bore 9 presacral vertebrae instead of the 8 of modern frogs.
Frog fossils have been found on all continents except Antarctica, but biogeographic evidence suggests they inhabited Antarctica when it was warmer.
Frogs have served as important model organisms throughout the history of science. Eighteenth-century biologist Luigi Galvani discovered the link between electricity and the nervous system through studying frogs. The African clawed frog or platanna (Xenopus laevis) was first widely used in laboratories in pregnancy assays in the first half of the 20th century. When human chorionic gonadotropin, a hormone found in substantial quantities in the urine of pregnant women, is injected into a female X. laevis, it induces them to lay eggs. In 1952, Robert Briggs and Thomas J. King cloned a frog by somatic cell nuclear transfer, the same technique later used to create Dolly the Sheep, their experiment was the first time successful nuclear transplantation had been accomplished in metazoans.
Frogs are used in cloning research and other branches of embryology because frogs are among the closest living relatives of man to lack egg shells characteristic of most other vertebrates, and therefore facilitate observations of early development. Although alternative pregnancy assays have been developed, biologists continue to use Xenopus as a model organism in developmental biology because it is easy to raise in captivity and has a large and easily manipulatable embryo. Recently, X. laevis is increasingly being displaced by its smaller relative X. tropicalis, which reaches its reproductive age in five months rather than one to two years (as in X. laevis), facilitating faster studies across generations. The genome sequence of X. tropicalis will probably be completed by 2015 at the latest.
The Moche people of ancient Peru worshipped animals and often depicted frogs in their art. In Panama local legend promised luck to anyone who spotted a golden frog in the wild and some believed that when Panamanian Golden Frogs died, they would turn into a gold talisman, known as a huaca. Today, despite being extinct in the wild, Panamanian Golden Frogs remain an important cultural symbol and can be found on decorative cloth molas made by the Kuna Indians, on T-shirts, as inlaid design on a new overpass in Panama City and even on lottery tickets.
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* Category:Articles containing video clips Category:Animals that can change color
ace:Cangguk af:Padda ar:ضفدع an:Anura az:Quyruqsuzlar bn:ব্যাঙ zh-min-nan:Chúi-ke be:Бясхвостыя земнаводныя be-x-old:Бясхвостыя bs:Žaba br:Anura bg:Безопашати земноводни ca:Anur cs:Žáby cy:Llyffant da:Frøer pdc:Frosch de:Froschlurche nv:Chʼał et:Päriskonnalised el:Βάτραχος es:Anura eo:Anuro eu:Anura fa:قورباغه hif:Medhak fr:Anoures ga:Frog gv:Rannag gl:Anuro gan:蝦蟆 glk:شوبوک hak:Kúai-é ko:개구리목 hi:मेंढक hr:Žabe id:Kodok dan katak iu:ᓈᕌᔩᖅ/naaraajiiq is:Froskar it:Anura he:חסרי זנב jv:Kodhok ka:ბაყაყი kk:Құйрықсыз қосмекенділер sw:Chura ht:Krapo ku:Beq la:Anura lv:Bezastainie abinieki lt:Beuodegiai varliagyviai li:Kwakkers en króddele hu:Békák mk:Жаба ml:തവള mr:बेडूक mzn:وک ms:Katak mdf:Ватракш mn:Мэлхий my:ဖား nl:Kikkers nds-nl:Kikvors ne:भ्यागुतो ja:カエル ce:Ph́id frr:Hobelfasker an poden no:Springpadder nn:Halelause padder nrm:Raînotte oc:Anura pnb:ڈڈو pl:Żaba pt:Anura ro:Broască qu:K'ayra rue:Жаба ru:Бесхвостые sah:Баҕа sq:Bretkoca simple:Frog sk:Žabotvaré sl:Žabe sr:Жабе sh:Žaba su:Bangkong fi:Sammakot sv:Stjärtlösa groddjur tl:Palaka ta:தவளை roa-tara:Marajòttole te:కప్ప th:กบ tg:Қурбоққа chr:ᏩᎶᏏ tr:Kuyruksuz kurbağalar uk:Безхвості ur:مینڈک vi:Bộ Không đuôi wa:Rinne (biesse) vls:Puut war:Pakla wuu:田鸡 yi:זשאבע yo:Kọ̀nkọ̀ zh-yue:蛙 zea:Puut'n zh:无尾目This text is licensed under the Creative Commons CC-BY-SA License. This text was originally published on Wikipedia and was developed by the Wikipedia community.
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