Hyla Temporal range: Eocene to recent | |
---|---|
European tree frog, Hyla arborea | |
Scientific classification | |
Domain: | Eukaryota |
Kingdom: | Animalia |
Phylum: | Chordata |
Class: | Amphibia |
Order: | Anura |
Family: | Hylidae |
Subfamily: | Hylinae |
Genus: | Hyla Laurenti, 1768 |
Species | |
See text | |
Synonyms [1] | |
|
Hyla is a genus of frogs in the tree frog family Hylidae. As traditionally defined, it was a wastebasket genus with more than 300 species found in Europe, Asia, Africa, and across the Americas. After a major revision of the family, most of these have been moved to other genera so that Hyla now only contains 17 extant (living) species from Europe, northern Africa and Asia. [2] The earliest known fossil member of this genus is † Hyla swanstoni from the Eocene of Saskatchewan, Canada, [3] but its designation to Hyla happened before the major revision, meaning that its position needs confirmation.
The genus was established by Josephus Nicolaus Laurenti in 1768. It was named after Hylas in Greek mythology, the companion of Hercules. The name is unusual in that – though Laurenti knew that Hylas was male – the name is unambiguously treated in the feminine grammatical gender for reasons unknown. The etymology of the name is also often incorrectly given as being derived from the Greek word ὕλη (hūlē, "forest" or "wood"). [4] [5]
Image | Binomial name | Common name | Distribution |
---|---|---|---|
H. annectans(Jerdon, 1870) | Jerdon's tree frog | northeast India (Assam, Nagaland, Manipur, and Meghalaya), northern Myanmar, and northern montane Vietnam and southwestern and central China (Yunnan, Guizhou, Sichuan, Hunan) | |
H. arborea(Linnaeus, 1758) | European tree frog | Albania; Armenia; Austria; Azerbaijan; Belarus; Belgium; Bosnia and Herzegovina; Bulgaria; Croatia; Cyprus; the Czech Republic; Denmark; France; Georgia; Germany; Greece; Hungary; Israel (found in the Ayalon Valley); Italy; Liechtenstein; Lithuania; Luxembourg; Macedonia, the Republic of; Moldova; Montenegro; the Netherlands; Poland; Portugal; Romania; the Russian Federation; Serbia; Slovakia; Slovenia; Sweden; Switzerland; Turkey; Ukraine. | |
H. carthaginiensisDufresnes, Beddek, Skorinov, Fumagalli, Perrin, Crochet, and Litvinchuk, 2019 | Carthaginian tree frog | northeastern Algeria and northwestern Tunisia. | |
H. chinensisGünther, 1858 | Common Chinese tree frog | southeastern and eastern China and in Taiwan | |
H. felixarabicaGvoždík, Moravec, Klütsch & Kotlík, 2010 | Arabian tree frog | Israel, Jordan, Saudi Arabia, Yemen, Syria and Lebanon. | |
H. hallowelliiThompson, 1912 | Hallowell's tree frog | Japan | |
H. intermediaBoulenger, 1882 | Italian tree frog | Italy, Slovenia, Switzerland, and possibly San Marino. | |
H. meridionalisBoettger, 1874 | Mediterranean tree frog | south-west Europe and north-west Africa | |
H. molleriBedriaga, 1889 | Moller's tree frog | Iberian Peninsula and southwesternmost France. | |
H. orientalis Bedriaga, 1890 | Oriental tree frog | Asia Minor and southeastern Europe | |
H. perriniDufresnes, Mazepa, Rodrigues, Brelsford, Litvinchuk, Sermier, Lavanchy, Betto-Colliard, Blaser, Borzée, Cavoto, Fabre, Ghali, Grossen, Horn, Leuenberger, Phillips, Saunders, Savary, Maddalena, Stöck, Dubey, Canestrelli, and Jeffries, 2018 | Perrin's tree frog | northern Italy, Switzerland (Ticino) and Slovenia | |
H. sanchiangensisPope, 1929 | San Chiang tree frog | China(Fujian, Guangdong, Guangxi, Guizhou, Anhui, Zhejiang, Hunan, Hubei, and Jiangxi) | |
H. sarda(De Betta, 1853) | Sardinian tree frog | Corsica, Sardinia, and the Tuscan Archipelago. | |
H. savignyiAudouin, 1827 | Middle East tree frog | Bulgaria, Armenia, Azerbaijan, Cyprus, Egypt, Georgia, Iran, Iraq, Israel, Jordan, Lebanon, Saudi Arabia, Syria, Turkey, and Yemen. | |
H. simplexBoettger, 1901 | Annam tree frog | southern China, Vietnam, and Laos | |
H. tsinlingensisLiu and Hu in Hu, Zhao, and Liu, 1966 | Shensi tree frog | China. | |
H. zhaopingensisTang and Zhang, 1984 | Zhaoping tree frog | China. | |
The mating systems across most species of Hyla largely feature female choice based on male calling effort. [6] [7] [8] The specific parameter of calling effort that is selected for can vary from species to species, however. In H. versicolor , for example, females show preference for calls of longer duration. [9] The selection of males which have calls of longer duration has shown to only be advantageous at low densities. This suggests that preference plasticity, based on environmental context, is beneficial. [9] Comparatively, males of H. arborea achieve a higher rate of mating success with increased chorus attendance, that is the number of nights spent calling at a given breeding site. [10] Moreover, increased chorus attendance carries with it a higher energy expenditure and risk of predation. Therefore, it may seem intuitive that males with higher chorus attendance are less likely to survive to the next breeding season. Conversely, these males are more likely to survive. This suggests that the fitness of these males is high enough to overcome the costs associated with chorus attendance. [10] This provides evidence for chorus attendance as an indicator of mate quality in H. arborea.
Although it is studied less frequently than female choice, sexual selection influenced by male-male intrasexual competition does exist in certain species of Hyla. Males of H. versicolor produce conspicuous advertisement calls in large groups at territories known to females. [11] This behavior, known as lekking, is common in many species of Hyla. In order to broadcast a clear acoustic communication to a female, males require distinct calling spaces within their respective leks. [11] When males infringe upon the calling space of one another, aggressive interactions may occur. Males of H. versicolor may choose to lower costs of aggressive encounters by first assessing one another's resource holding potential. [12] In simple terms, the resource holding potential (RHP) of an individual is its ability to win a fight. RHP can be based on a number of factors, including mass, size, weaponry, etc. In H. versicolor, the question of what determines an individual's RHP still stands. Aggressive interactions of this species are hard to observe within natural environments, because they occur briefly and infrequently. [11] Research has suggested that RHP in this species is not based on body size, however these findings were not based on in situ observations, but instead on the findings of a manipulated experiment. [12]
In terms of sexual selection, indirect selection refers to the selection of a specific trait based on its genetic correlation to overall fitness. H. arborea is a nocturnal species which depends on calling by males for female mate choice. [7] [9] In addition to its ability to detect acoustic communications, H. arborea, as well as most other Anuran species, possess specialized visual systems that function particularly well in low light. [13] This visual system allows for detection of observable male traits that could factor into female mate choice. Research has shown that H. arborea females have a preference for males with more conspicuous vocal sac coloration. [13] It is postulated that this preference may assist in localization and detection of males by searching females. However, vocal sac pigmentation is dictated by carotenoid levels, which must be ingested through food intake. [13] Thus, the presence of conspicuous vocal sac coloration could in turn signal higher male foraging ability and fitness. [13]
Sexual selection is a mode of natural selection in which members of one biological sex choose mates of the other sex to mate with, and compete with members of the same sex for access to members of the opposite sex. These two forms of selection mean that some individuals have greater reproductive success than others within a population, for example because they are more attractive or prefer more attractive partners to produce offspring. Successful males benefit from frequent mating and monopolizing access to one or more fertile females. Females can maximise the return on the energy they invest in reproduction by selecting and mating with the best males.
Amplexus is a type of mating behavior exhibited by some externally fertilizing species 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. In amphibians, females may be grasped by the head, waist, or armpits, and the type of amplexus is characteristic of some taxonomic groups.
A lek is an aggregation of male animals gathered to engage in competitive displays and courtship rituals, known as lekking, to entice visiting females which are surveying prospective partners with which to mate. A lek can also indicate an available plot of space able to be utilized by displaying males to defend their own share of territory for the breeding season. A lekking species is characterised by male displays, strong female mate choice, and the conferring of indirect benefits to males and reduced costs to females. Although most prevalent among birds such as black grouse, lekking is also found in a wide range of vertebrates including some bony fish, amphibians, reptiles, and mammals, and arthropods including crustaceans and insects.
Behavioral ecology, also spelled behavioural ecology, is the study of the evolutionary basis for animal behavior due to ecological pressures. Behavioral ecology emerged from ethology after Niko Tinbergen outlined four questions to address when studying animal behaviors: What are the proximate causes, ontogeny, survival value, and phylogeny of a behavior?
Hylidae is a wide-ranging family of frogs commonly referred to as "tree frogs and their allies". However, the hylids include a diversity of frog species, many of which do not live in trees, but are terrestrial or semiaquatic.
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 gray treefrog is a species of small arboreal holarctic tree frog native to much of the eastern United States and southeastern Canada.
Cope's gray treefrog is a species of treefrog found in the United States and Canada. It is almost indistinguishable from the gray treefrog, and shares much of its geographic range. Both species are variable in color, mottled gray to gray-green, resembling the bark of trees. These are treefrogs of woodland habitats, though they will sometimes travel into more open areas to reach a breeding pond. The only readily noticeable difference between the two species is the mating call — Cope's has a faster-paced and slightly higher-pitched call than D. versicolor. In addition, D. chrysoscelis is reported to be slightly smaller, more arboreal, and more tolerant of dry conditions than D. versicolor.
The squirrel tree frog is a small species of tree frog found in the south-eastern United States, from Texas to Virginia. This is an introduced species in the Bahamas. Squirrel tree frogs are small frogs, about 1.5 inches in length as adults. There are several color variations, but most commonly they are green and look very much like the American green tree frog. They can also be varying shades of yellow or brown, sometimes with white or brown blotching.
Teleogryllus oceanicus, commonly known as the Australian, Pacific or oceanic field cricket, is a cricket found across Oceania and in coastal Australia from Carnarvon in Western Australia and Rockhampton in north-east Queensland
Dryophytes gratiosus, commonly known as the barking tree frog, is a species of tree frog endemic to the south-eastern United States.
Mate choice is one of the primary mechanisms under which evolution can occur. It is characterized by a "selective response by animals to particular stimuli" which can be observed as behavior. In other words, before an animal engages with a potential mate, they first evaluate various aspects of that mate which are indicative of quality—such as the resources or phenotypes they have—and evaluate whether or not those particular trait(s) are somehow beneficial to them. The evaluation will then incur a response of some sort.
Dendropsophus ebraccatus, also known as the hourglass treefrog, referring to the golden-brown hourglass shape seen surrounded by skin yellow on its back. Their underbellies are yellow. Their arms and lower legs usually display bold patterns while their upper legs or thighs are light yellow giving them the appearance of wearing no pants. The species name "ebraccata" translates to "without trousers" in Latin.
The Italian tree frog is a species of frog in the family Hylidae, found in Italy, Slovenia, Switzerland, and possibly San Marino. Its natural habitats are temperate forests, rivers, intermittent rivers, freshwater marshes, intermittent freshwater marshes, arable land, and urban areas. It is threatened by habitat loss.
A courtship display is a set of display behaviors in which an animal, usually a male, attempts to attract a mate; the mate exercises choice, so sexual selection acts on the display. These behaviors often include ritualized movement ("dances"), vocalizations, mechanical sound production, or displays of beauty, strength, or agonistic ability.
Female copulatory vocalizations, also called female copulation calls or coital vocalizations, are produced by female primates, including human females, and female non-primates. Copulatory vocalizations usually occur during copulation and are hence related to sexual activity. Vocalizations that occur before intercourse, for the purpose of attracting mates, are known as mating calls.
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.
Reproductive interference is the interaction between individuals of different species during mate acquisition that leads to a reduction of fitness in one or more of the individuals involved. The interactions occur when individuals make mistakes or are unable to recognise their own species, labelled as ‘incomplete species recognition'. Reproductive interference has been found within a variety of taxa, including insects, mammals, birds, amphibians, marine organisms, and plants.
The sensory trap hypothesis describes an evolutionary idea that revolves around mating behavior and female mate choice. It is a model of female preference and male sexual trait evolution through what is known as sensory exploitation. Sensory exploitation, or a sensory trap is an event that occurs in nature where male members of a species perform behaviors or display visual traits that resemble a non-sexual stimulus which females are responsive to. This tricks females into engaging with the males, thus creating more mating opportunities for males. What makes it a sensory trap is that these female responses evolved in a non-sexual context, and the male produced stimulus exploits the female response which would not otherwise occur without the mimicked stimulus.