Microhyla Tschudi, 1838

Class: Amphibia > Order: Anura > Family: Microhylidae > Subfamily: Microhylinae > Genus: Microhyla
42 species

Microhyla Tschudi, 1838, Classif. Batr.: 71. Type species: "Hylaplesia achatina Boie, 1827" (nomen nudum) (= Microhyla achatina Tschudi, 1838), by monotypy.

MicrhylaDuméril and Bibron, 1841, Erp. Gen., 8: 28, 613. Unjustified emendation of Microhyla Tschudi, 1838.

Siphneus Fitzinger, 1843, Syst. Rept.: 19. Type species: Engystoma ornatum Duméril and Bibron, 1841, by original designation. Preoccupied by Siphneus Brants, 1827. Synonymy by Stejneger, 1907, Bull. U.S. Natl. Mus., 58: 87.

Dendromanes Gistel, 1848, Naturgesch. Thierr.: xi. Substitute name for Microhyla Tschudi, 1838.

Diplopelma Günther, 1859 "1858", Cat. Batr. Sal. Coll. Brit. Mus.: 50. Replacement name for Siphneus Fitzinger, 1843. Synonymy by Boulenger, 1882, Cat. Batr. Sal. Coll. Brit. Mus., Ed. 2: 164. Synonymy by Boulenger, 1882, Cat. Batr. Sal. Coll. Brit. Mus., Ed. 2: 164.

Scaptophryne Fitzinger, 1861 "1860", Sitzungsber. Akad. Wiss. Wien, Phys. Math. Naturwiss. Kl., 42: 416. Type species: Scaptophryne labyrinthica Fitzinger, 1861 "1860. Nomen nudum. Synonymy by Boulenger, 1882, Cat. Batr. Sal. Coll. Brit. Mus., Ed. 2: 164.

Copea Steindachner, 1864, Verh. Zool. Bot. Ges. Wien, 14: 286. Type species: Copea fulva Steindachner, 1864, by monotypy. Synonymy by Parker, 1932, Ann. Mag. Nat. Hist., Ser. 10, 10: 341.

Ranina David, 1872 "1871", Nouv. Arch. Mus. Natl. Hist. Nat. Paris, 7: 76. Type species: Ranina symetrica David, 1871, by monotypy. Junior homonym of Ranina Lamarck, 1801. Synonymy by Boulenger, 1882, Cat. Batr. Sal. Coll. Brit. Mus., Ed. 2: 164.

English Names

Rice Frogs (Frank and Ramus, 1995, Compl. Guide Scient. Common Names Amph. Rept. World: 90).

Distribution

Ryukyu Is. (Japan) and China south through India to Sri Lanka and through Southeast Asia to Sumatra, Borneo, Java, and Bali.

Comment

Taylor, 1962, Univ. Kansas Sci. Bull., 43: 539–563, reviewed the species in Thailand. Inger, 1966, Fieldiana, Zool., 52: 145–155, reviewed the Bornean species. Bourret, 1942, Batr. Indochine: 508–529, reviewed the Indochinese species. Liu and Hu, 1961, Tailless Amph. China: 295-304, reviewed the Chinese species. See Dubois, 1987, Alytes, 6: 1–9, for the subgenera (Diplopelma and Microhyla) and species group taxonomy used herein. See identification table by Manthey and Grossmann, 1997, Amph. Rept. Südostasiens: 46, to compare the species in the Sunda Shelf region. Malkmus, Manthey, Vogel, Hoffmann, and Kosuch, 2002, Amph. Rept. Mount Kinabalu: 131, provided a key to the species of Borneo. Fei, Hu, Ye, and Huang, 2009, Fauna Sinica, Amph. 2: 883-916, provided a key, accounts, and spot maps for China. Matsui, Hamidy, Belabut, Ahmad, Panha, Sudin, Khonsue, Oh, Yong, Jiang, and Nishikawa, 2011, Mol. Phylogenet. Evol., 61: 167–176, suggested on the basis of mtDNA that Microhyla may be paraphyletic, with a clade composed of Calluella and Glyphoglossus imbedded within it. Pyron and Wiens, 2011, Mol. Phylogenet. Evol., 61: 543–583, in their study of Genbank sequences, suggested their set of exemplar species to be monophyletic and the sister taxon of Glyphoglossus + Calluella. Poyarkov, Vassilieva, Orlov, Galoyan, Tran, Le, Kretova, and Geissler, 2014, Russ. J. Herpetol., 21: 89–148, rejected the subgenera formulated by Dubois, 1987, Alytes, 6: 1–9, as artificial but did discuss the provisional nature of the infrageneric taxonomy at present and the seeming conflict of morphology and molecules; these authors also provided and identification key and comments regarding systematics of the species found in Vietnam. Manthey and Denzer, 2014, Sauria, Berlin, 36: 3–21, discussed the species of Southeast Asia and provided natural history and systematic information. Yong, Song, Lim, Eamsobhana, and Tan, 2016, Biochem. Syst. Ecol., 66: 243–253, found Microhyla to be monophyletic on the basis of 13 protein-coding genes. Yuan, Suwannapoom, Yan, Poyarkov, Nguyen, Chen, Chomdej, Murphy, and Che, 2016, Curr. Zool., Chengdu, 62: 531–543, on the basis of molecular analysis, provided a discussion of Pleistocene climatic fluctuations on how they shaped the genetic structre of the Microhyla fissipes complex (Microhyla mukhlesuri and Microhyla fissipes).  Garg, Das, Kamei, and Biju, 2018, MtDNA, Part B, 3: 856–861, addressed the Microhyla ornata complex via DNA barcodes, and provided generalized range maps. The complex turned out to be fictitious in the sense that the Microhyla muklesuri + Microhyla mumensinghensis group, is distant from the Microhyla nilphamariensis + Microhyla teraiensis + Microhyla ornata group. 

Contained taxa (42 sp.):

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