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~ Kazekage Sasori ~
Frogs are amphibians in the order Anura (meaning "tail-less", from Greek an-, without + oura, tail), formerly referred to as Salientia (Latin saltare, to jump). Most frogs are characterized by long hind legs, 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 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".

The name frog derives from Old English frogga, (compare Old Norse frauki, German Frosch, older Dutch spelling kikvorsch), cognate with Sanskrit plava (frog), probably deriving from Proto-Indo-European praw = "to jump".[1]

Contents [hide]
1 Taxonomy
2 Morphology and physiology
2.1 Feet and legs
2.2 Jumping
2.3 Skin
2.4 Poison
2.5 Respiration and circulation
2.6 Digestion and excretion
2.7 Nervous system
3 Natural history
3.1 Life cycle
3.2 Reproduction of frogs
3.3 Parental care
3.4 Call
4 Distribution and conservation status
5 Evolution
6 Uses in agriculture and research
7 Cultural beliefs
8 See also
9 Cited references
10 General references
11 External links
11.1 Media


Taxonomy
For more details on this topic, see List of Anuran families.
The order Anura contains 4,810 species[2] in 33 families, of which the Leptodactylidae (1100 spp.), Hylidae (800 spp.) and Ranidae (750 spp.) are the richest in species. About 88% of amphibian species are frogs.


European Fire-bellied Toad (Bombina bombina)The use of the common names "frog" and "toad" has no taxonomic justification. From a taxonomic perspective, all members of the order Anura are frogs, but only members of the family Bufonidae are considered "true toads". The use of the term "frog" in common names usually refers to species that are aquatic or semi-aquatic with smooth and/or moist skins, and the term "toad" generally refers to species that tend to be terrestrial with dry, warty skin. An exception is the fire-bellied toad (Bombina bombina): while its skin is slightly warty, it prefers a watery habitat.

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.[3] 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.[4]

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.

Morphology and physiology

Skeleton of RanaThe morphology of frogs is unique among amphibians. Compared with the other two groups of amphibians, (salamanders and caecilians), frogs are unusual because they lack tails as adults and their legs are more suited to jumping than walking. The physiology of frogs is generally like that of other amphibians (and differs from other terrestrial vertebrates) because oxygen can pass through their highly permeable skin. This unique feature allows frogs to "breathe" largely through their skin.[citation needed] Because the oxygen is dissolved in an aqueous film on the skin and passes from there to the blood, the skin must remain moist at all times; this makes frogs susceptible to many toxins in the environment, some of which can similarly dissolve in the layer of water and be passed into their bloodstream. This may be the cause of the decline in frog populations.[citation needed]

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.[citation needed]

Frogs range in size from 10 mm (0.39 in) (Brachycephalus didactylus of Brazil and Eleutherodactylus iberia of Cuba) to 300 mm (12 in) (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 do in fact have teeth of a sort. They have a ridge of very small cone teeth around the upper edge of the jaw. These are called maxillary teeth. Frogs often also have what are called vomerine teeth on the roof of their mouth. They do not have anything that could be called teeth on their lower jaw, so they usually swallow their food whole. The so-called "teeth" are mainly used to hold the prey and keep it in place till they can get a good grip on it and squash their eyeballs down to swallow their meal. Toads, however, do not have any teeth.[citation needed]

Feet and legs

Tyler's Tree Frog (Litoria tyleri) illustrates large toe pads and webbed feet
A bullfrog skeleton, showing elongate limb bones and extra joints. Red marks indicate bones which have been substantially elongated in frogs and joints which have become mobile. Blue indicates joints and bones which have not been modified or only somewhat elongated.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.[5]

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.[6]

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.[7]

Jumping
Frogs are generally recognized as exceptional jumpers, and the best jumper of all vertebrates. The Australian rocket frog, Litoria nasuta, can leap over 50 times its body length (5.5 cm), resulting in jumps of over 2 meters. The acceleration of the jump may be up to twice gravity. There are tremendous differences between species in jumping capability, but within a species, jump distance increases with increasing size, but relative jumping distance (body-lengths jumped) decreases.

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.[citation needed]

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.[citation needed]

Skin

Pouched Frog (Assa darlingtoni) camouflaged against leaf litter.
Microscopic view of frog skinMany 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.[citation needed]

Certain frogs change colour between night and day, as light and moisture stimulate the pigment cells and cause them to expand or contract.

Poison

Oophaga pumilio, a poison dart frog, contains numerous alkaloids which deter predatorsMany frogs contain mild toxins that make them unpalatable to potential predators. For example, all toads have large poison glands—the parotoid glands—located behind the eyes on the top of the head. Some frogs, such as some poison dart frogs, are especially toxic. The chemical makeup of toxins in frogs varies from irritants to hallucinogens, convulsants, nerve poisons, and vasoconstrictors. Many predators of frogs have adapted to tolerate high levels of these poisons. Others, including humans, may be severely affected.

Some frogs obtain poisons from the ants and other arthropods they eat;[8] others, such as the Australian Corroboree Frogs (Pseudophryne corroboree and Pseudophryne pengilleyi), can manufacture an alkaloid not derived from their diet.[9] Some native people of South America extract poison from the poison dart frogs and apply it to their darts for hunting,[10] 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).[11][12]

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.[13] Arrow and dart poisons are under active investigation for their potential as therapeutic drugs.[14]

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.

Respiration and circulation
The skin of a frog is permeable to oxygen and carbon dioxide, as well as to water. There are a number of blood vessels near the surface of the skin. When a frog is underwater, oxygen is transmitted through the skin directly into the bloodstream. On land, adult frogs use their lungs to breathe. Their lungs are similar to those of humans, but the chest muscles are not involved in respiration, and there are no ribs or diaphragm to support breathing. Frogs breathe by taking air in through the nostrils (which often have valves which close when the frog is submerged), causing the throat to puff out, then compressing the floor of the mouth, which forces the air into the lungs. In August 2007 an aquatic frog named Barbourula kalimantanensis was discovered in a remote part of Indonesia. The Bornean Flat-headed Frog (B. kalimantanensis) is the first species of frog known to science without lungs.

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.[15]

Digestion and excretion
The frog's digestive system begins with the mouth. Frogs have teeth along their upper jaw called the maxillary teeth, which are used to grind food before swallowing. These teeth are very weak, and cannot be used to catch or harm agile prey. Instead, the frog uses its sticky tongue to catch food (such as flies or other insects). The food then moves through the esophagus into the stomach. The food then proceeds to the small intestine (duodenum and ileum) where most digestion occurs. Frogs carry pancreatic juice from the pancreas, and bile (produced by the liver) through the gallbladder from the liver to the small intestine, where the fluids digest the food and extract the nutrients. When the food passes into the large intestine, the water is reabsorbed and wastes are routed to the cloaca. All wastes exit the body through the cloaca and the cloacal vent.

Nervous system
The frog has a highly developed nervous system which consists of a brain, spinal cord and nerves. Many parts of the frog's brain correspond with those of humans. The medulla oblongata regulates respiration, digestion, and other automatic functions. Muscular coordination and posture are controlled by the cerebellum. The relative size of the cerebrum of a frog is much smaller than that of a human. Frogs have ten cranial nerves (nerves which pass information from the outside directly to the brain) and ten pairs of spinal nerves (nerves which pass information from extremities to the brain through the spinal cord). By contrast, all amniotes (mammals, birds and reptiles) have twelve cranial nerves. Frogs do not have external ears; the eardrums (tympanic membranes) are directly exposed. As in all animals, the ear contains semicircular canals which help control balance and orientation.





 
 
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