Amplexus (Latin "embrace") is a type of mating behavior exhibited by some externally fertilizing species (chiefly amphibians and horseshoe crabs) in which a male grasps a female with his front legs as part of the mating process, and at the same time or with some time delay, he fertilizes the eggs, as they are released from the female's body. [1] In amphibians, females may be grasped by the head, waist, or armpits, and the type of amplexus is characteristic of some taxonomic groups.
Amplexus involves direct contact between male and female, distinguished from other forms of external fertilization, such as broadcast spawning, where sperm and eggs are freely shed into water without direct contact by individuals. In order for amplexus to be initiated, male frogs must first find a mate by attracting one through calls, typically in the evening. [2] Once a male has successfully attracted a mate, the process of amplexus begins, while the unsuccessful males are forced to continue their search for a mate through further calls. [2]
The competition for a female mate among males is considered intense, and it is not uncommon for a male amphibian to attack an already-amplexed pair of amphibians. [3] When a male amphibian attacks an amplexed pair of amphibians, he is trying to force the other male to release its grasp of the female, so he can then mate with her. [3] Male amphibians are also known to show mate-guarding behaviour, which is shown after amplexus, and it is the male's attempt to prevent the female amphibian from mating with other males. [3]
The duration of amplexus has been found to vary across species. In some species it may last for many days, while in others it may last a few hours. [4] Despite the variation in the duration of amplexus across species, typically all species that exhibit this behaviour have to use their forelimb muscles for the duration of amplexus. [4] Studies have found that this reproductive behaviour of amplexus can come with different fitness costs, due to the fact that amplexus can occur for prolonged periods of time. For instance, a study found that when a male amphibian is grasping and holding onto a female amphibian, this can lead to the impairment of the female's ability to move or to feed. [5] After conducting experiments, researchers confirmed that amplexus does decrease a female's locomotor performance (e.g., swimming, walking) as well as the feeding rates. [5] With regard to the cost to the male engaged in amplexus, male amphibians have been found to not feed at all during amplexus. [5]
Many types of amplexus are identified in the literature. However, two types of amplexus are more common than others, known as inguinal and axillary amplexus. [6] These two types of amplexus have been classified based on the position of the male amphibian relative to the female. [6] When a male amphibian clasps a female around her waist (inguinal region) using his forelimbs, this is considered inguinal amplexus. [6] By contrast, when a male amphibian clasps behind the forelimbs (axillary region) of the female, this is considered axillary amplexus. [6]
Amplexus has been found to involve different muscles in both male and female amphibians. The forelimb muscles in both males and females have been identified as the key muscles for amplexus that most species use. [4] These forelimb muscles that are used during amplexus are typically larger in males than females, and for males these muscles contain more oxidative fibers, which could mean that amplexus involves an increased rate of aerobic metabolism. [4] In addition to those forelimb muscles being larger in males, male frogs also typically have keratin pads or nuptial pads, which are located on their thumbs and contribute to the success of amplexus by assisting in gripping the female for the duration of amplexus. [7] This amplexus behaviour allows the amphibians' cloacae to be in close contact, while gametes are released. [8] Additionally, amplexus is thought to help with the alignment of the reproductive tracts of both males and females, which furthermore contributes to successful fertilization. [1] A female amphibian may not always be receptive to a male amphibian who is trying to initiate amplexus, as the female may not be ready to produce eggs. [1] When the female is not ready to engage in amplexus, she will simply vibrate her body, which will then be felt by the male who is clasped to her and he will then stop the amplexus behaviour. [1]
Two major hormones have been identified to be involved in amplexus. The hormone arginine vasotocin (AVT) has been identified as having an effect on the calling behaviours produced by these male amphibians when searching for a female mate, as AVT increased the amount of calling behaviour produced in male amphibians. [8] Additionally, it is believed that the gonadotropin-releasing hormone (GnRH) has an influence on amplexus in amphibians, as it has been found to produce or initiate this behaviour in many anuran amphibians. [8] Furthermore, both arginine vasotocin and gonadotropin-releasing hormone have been found to be involved in the sexual behaviour of male amphibians. [8] The stress hormone corticosterone has also been identified as associated with the sexual behaviour of amplexus. A study conducted on red-spotted newts found an acute increase in corticosterone for both males and females who were engaged in the behaviour of amplexus. [9] However, overall it was found that males have a higher level of corticosterone compared to females, as amplexus is seen as more energetically costly to males. [9] The increase in corticosterone found in females could be attributed to amplexus preventing them from foraging for food. [9]
Amplexus chiefly occurs aquatically, but some terrestrial anurans (frogs and toads) like the disc-tongued frogs (Discoglossidae) perform amplexus on land. In crown-group anurans, like the true frogs (Ranidae), the tree frogs (Hylidae), and the true toads (Bufonidae), amplexus is axillary (in the armpits). Other anurans (the Archaeobatrachia, Sooglossidae and Myobatrachidae), show the ancestral state which is inguinal or lumbar amplexus (abdominal, in front of the hindlegs). Some species show cephalic amplexus where the head of the female is held while others show complete lack of amplexus. [10] Additionally, anurans species have been observed to engage in multiple amplexus, which can also be referred to as a mating ball, as many toads attach themselves to a female trying to initiate amplexus. [11] However, multiple amplexus is not common among anurans, which could indicate that the costs associated with multiple amplexus are higher than the advantages associated with it. [11] For female anurans, the idea of multiple amplexus would probably be more advantageous, because mating with more than one male would increase fertilization chances or increase offspring genetic diversity. [11] Multiple amplexus would typically be common in explosive breeding amphibians, when there is a larger number of adults ready to breed at a breeding site in a short period of time. [1] When this occurs female amphibians are viewed as a very important resource for males, as there are typically more males present than females, thus leading to more chances for multiple amplexus to occur. [1]
In most anurans, the males deposit sperm onto the eggs as they are being laid, however males of the genus Ascaphus possess an intromittent organ, unique among anurans, for internal fertilization. Internal fertilization does occur in a few other genera, including Nectophrynoides , Mertensophryne , and Eleutherodactylus . [10] [12]
In the case of newts, the process of amplexus is often observed soon after the newts become seasonally active. In the Western USA, for example, this time is typically soon after the onset of the winter rainy season, when intermittent streams and vernal pools become available as a breeding habitat. The rough-skinned newt is a specific widespread example of a newt in the western USA that can be observed in quiet stream pools and shallow ponds engaging in amplexus. [13] During amplexus in newts, males will typically show the behaviour of tail fanning and chin rubbing which is thought to prompt the mating receptivity of the female newt. [14] Studies have shown that male newts who have deeper tail-fins have better control of females during amplexus and are also more successful in catching the females for amplexus. [14] Additionally, it has been found that the probability of a male newt who has a deeper tail-fin to achieve amplexus is greater than those newts who do not contain a deeper tail-fin, as male newts tend to use their tails during male-male competition. [14] When a male newt, who is unpaired, encounters a female and male newt engaged in amplexus, the unpaired newt will try to displace the paired male newt by using wrestling tactics. [15] A study examining the wrestling behaviour of newts found that of the observed wrestling encounters, 90% were "won" by the paired male, meaning he would retain the female newt. [15] The study found that the invading unpaired newt rarely successfully displaces the paired male newt, engaged in amplexus. [15]
Amplexus occurs in all four species of horseshoe crab. Horseshoe crabs typically go ashore for amplexus in high tide, and end up on beaches where the eggs are more protected. [16] The first pair of walking legs is used to tightly clasp the female in all species, and the second pair is also employed in all but Limulus polyphemus . [17] A male horseshoe crab develops modified claspers during sexual maturity when the male moults; these modified claspers can then help during the process of amplexus. [18] The male's pair of posterior claspers are known for having the ability to maintain long-term amplexus which have been found to always attach to the female's opisthosoma during amplexus. [18] In contrast, the male's anterior claspers have been found to attach to the female's opisthosoma as well, but on the lateral edges of the opisthosoma and function to resist displacement from environmental factors. [18] Uniquely, amplexus is most likely to occur between horseshoe crabs when the female horseshoe crab has a hard shell. [18] Additionally, males who inhabit a clean shell are more likely to enter amplexus, compared to males who contain a dirty shell, as it seems that females have a preference for clean shells on males. [18] A male horseshoe crab's claspers may also be an important factor of consideration for the initiation of amplexus. Since claspers are used for the attachment to the female, claspers that are in good condition are more successful for the initiation of amplexus. [19] If a male horseshoe crab has a damaged or missing clasper, then that puts the male at a disadvantage and increases the probability of being displaced by other competing male crabs. [19]
Fossil evidence suggests that a certain euthycarcinoid (an extinct arthropod) from the Cambrian may also have mated by amplexus. [20]
The American bullfrog, often simply known as the bullfrog in Canada and the United States, is a large true frog native to eastern North America. It typically inhabits large permanent water bodies such as swamps, ponds, and lakes. Bullfrogs can also be found in manmade habitats such as pools, koi ponds, canals, ditches and culverts. The bullfrog gets its name from the sound the male makes during the breeding season, which sounds similar to a bull bellowing. The bullfrog is large and is commonly eaten throughout its range, especially in the southern United States where they are plentiful.
The tailed frogs are two species of frogs in the genus Ascaphus, the only taxon in the family Ascaphidae. The "tail" in the name is actually an extension of the male cloaca. The tail is one of two distinctive anatomical features adapting the species to life in fast-flowing streams. These are the only North American frog species that reproduce by internal fertilization. They are among the most primitive known families of frogs.
The eastern newt is a common newt of eastern North America. It frequents small lakes, ponds, and streams or nearby wet forests. The eastern newt produces tetrodotoxin, which makes the species unpalatable to predatory fish and crayfish. It has a lifespan of 12 to 15 years in the wild, and it may grow to 5 in (13 cm) in length. These animals are common aquarium pets, being either collected from the wild or sold commercially. The striking bright orange juvenile stage, which is land-dwelling, is known as a red eft. Some sources blend the general name of the species and that of the red-spotted newt subspecies into the eastern red-spotted newt.
External fertilization is a mode of reproduction in which a male organism's sperm fertilizes a female organism's egg outside of the female's body. It is contrasted with internal fertilization, in which sperm are introduced via insemination and then combine with an egg inside the body of a female organism. External fertilization typically occurs in water or a moist area to facilitate the movement of sperm to the egg. The release of eggs and sperm into the water is known as spawning. In motile species, spawning females often travel to a suitable location to release their eggs.
Agalychnis callidryas, commonly known as the red-eyed tree frog, is a species of frog in the subfamily Phyllomedusinae. It is native to forests from Central America to north-western South America. This species is known for its bright coloration, namely its vibrant green body with blue and yellow stripes on the side. It has a white underside, brightly red and orange colored feet, and is named after its distinctive bright red eyes.
The American green tree frog is a common arboreal species of New World tree frog belonging to the family Hylidae. This nocturnal insectivore is moderately sized and has a bright green to reddish-brown coloration. Commonly found in the central and southeastern United States, the frog lives in open canopy forests with permanent water sources and abundant vegetation. When defending its territory, the frog either emits aggressive call signals or resolves to grapple with intruders, seldom leading to injury or death. To avoid predation, the frog will leap into the water or jump into the treetops.
Hyla japonica, commonly known as the Japanese tree frog, is a species of anuran native to Japan, China, and Korea. H. japonica is unique in its ability to withstand extreme cold, with some individuals showing cold resistance at temperatures as low as −30 °C for up to 120 days. H. japonica are not currently facing any notable risk of extinction and are classified by the IUCN as a species of "least concern". Notably, H. japonica have been sent to space in a study that explored the effect of microgravity on H. japonica. Hyla japonica is synonymous with Dryophytes japonicus.
The plains spadefoot toad is a species of American spadefoot toad which ranges from southwestern Canada, throughout the Great Plains of the western United States, and into northern Mexico. Like other species of spadefoot toads, they get their name from a spade-like projection on their hind legs which allows them to dig into sandy soils. Their name, in part, comes from their keratinized metatarsals, which are wide instead of "sickle shaped". The species name translates as buzzing leaf shaped. This refers to the species' distinguishing features; its buzzing mating call, and its leaf-shaped digging metatarsals. It was first described by Cope in 1863.
The Japanese common toad, Japanese warty toad or Japanese toad is a species of toad in the family Bufonidae. It is endemic to Japan. Its natural habitats are subarctic forests, temperate forests, temperate shrubland, swamps, freshwater marshes, intermittent freshwater marshes, freshwater springs, arable land, rural gardens, urban areas, ponds, and irrigated land. Amplexus is the mating behaviour involved in the Japanese common toad during the breeding season.
Allobates femoralis is a species of frog in the family Aromobatidae. It is found in Bolivia, Brazil, Colombia, Ecuador, French Guiana, Guyana, Peru, and Suriname. Its natural habitat is tropical lowland forests.
Rosenberg's treefrog, also known as Rosenberg's gladiator frog or Rosenberg's gladiator treefrog, is a species of frog in the family of tree frogs (Hylidae) and genus of gladiator frogs (Boana) found in Costa Rica, Panama, Colombia, Trinidad and Tobago and north-western Ecuador. Its scientific name is a testimony to Mr. W. F. H. Rosenberg who collected the type series, and its common name refers to the aggressiveness of males of the species.
The Panama cross-banded tree frog or pug-nosed tree frog is a species of frog in the family Hylidae found in the humid Pacific lowlands of southwestern Costa Rica to eastern Panama and in the Caribbean lowlands of Panama and northern Colombia. Males of the species utilize synchronous calling to hide their position from predators. Females create basins during amplexus and deposit fertilized eggs onto the surface of the water.
The Túngara frog is a species of frog in the family Leptodactylidae. It is a small nocturnal terrestrial frog found in Mexico, Central America, and the northeastern regions of South America.
The climbing mantella is a species of diurnal poison frog of the genus Mantella that resides in the subtropical regions of northeast Madagascar. Although it spends a significant amount of time in trees or bamboo forests, this frog species is not fully arboreal and actively seeks areas with a water source.
The grey foam-nest tree frog, or southern foam-nest tree frog, is a species of frog in the family Rhacophoridae. They are found in southern Africa.
Lithobates clamitans or Rana clamitans, commonly known as the green frog, is a species of frog native to eastern North America. The two subspecies are the bronze frog and the northern green frog.
A nuptial pad is a secondary sex characteristic present on some mature male frogs and salamanders. Triggered by androgen hormones, this breeding gland appears as a spiked epithelial swelling on the forearm and prepollex that aids with grip, which is used primarily by males to grasp females during amplexus. They can also be used in male–male combat in some species.
The Ranoidea are a superfamily of frogs in the order Anura. Members of this superfamily are characterised by having the pectoral girdle fused into a single complex unit, having no ribs, and using an axillary grip during amplexus. The larvae have a single spiracle on the left side and complex mouthparts, or in some species, undergo direct development. The taxonomy of these families has been under heavy debate for many years. In recent studies, molecular data has been used to better identify the phylogentic relationships of these frogs, rearranging and introducing new subfamilies to better distinguish between large groups of frogs.
Sexual selection in amphibians involves sexual selection processes in amphibians, including frogs, salamanders and newts. Prolonged breeders, the majority of frog species, have breeding seasons at regular intervals where male-male competition occurs with males arriving at the waters edge first in large number and producing a wide range of vocalizations, with variations in depth of calls the speed of calls and other complex behaviours to attract mates. The fittest males will have the deepest croaks and the best territories, with females making their mate choices at least partly based on the males depth of croaking. This has led to sexual dimorphism, with females being larger than males in 90% of species, males in 10% and males fighting for groups of females.
The femoral gland is a specialised gland found in some male frogs that plays a role in chemical communication and reproductive signalling. Particularly prominent within the frog family Mantellidae, these glands are located on the underside of the hindlimbs, usually on the inner thighs or shanks. Femoral glands can be identified by their swollen appearance and distinct colouration, which differ from the surrounding skin. Femoral glands are classified into four distinct morphological types, varying from minute granular structures to conspicuous patches characterised by large granules and prominent central indentations.