Crayfish are freshwater crustaceans belonging to the clade Astacidea, which also contains lobsters. Taxonomically, they are members of the superfamilies Astacoidea and Parastacoidea. They breathe through feather-like gills. Some species are found in brooks and streams, where fresh water is running, while others thrive in swamps, ditches, and paddy fields. Most crayfish cannot tolerate polluted water, although some species, such as Procambarus clarkii, are hardier. Crayfish feed on animals and plants, either living or decomposing, and detritus.
Astacus is a genus of crayfish found in Europe and western Asia, comprising three extant (living) species and three extinct fossil species.
Reptantia is a clade of decapod crustaceans named in 1880 which includes lobsters, crabs and many other well-known crustaceans.
Pleocyemata is a suborder of decapod crustaceans, erected by Martin Burkenroad in 1963. Burkenroad's classification replaced the earlier sub-orders of Natantia and Reptantia with the monophyletic groups Dendrobranchiata (prawns) and Pleocyemata. Pleocyemata contains all the members of the Reptantia, as well as the Stenopodidea, and Caridea, which contains the true shrimp.
Pontastacus is a genus of freshwater crayfish occurring in eastern Europe and western Asia.
Astacidea is an infraorder of decapod crustaceans including lobsters, crayfish, and their close relatives.
The Parastacidae are the family of freshwater crayfish found in the Southern Hemisphere. The family is a classic Gondwana-distributed taxon, with extant members in South America, Madagascar, Australia, New Zealand, and New Guinea, and extinct taxa also in Antarctica.
Raninoida is a taxonomic section of the crabs, containing a single superfamily, Raninoidea. This group of crabs is unlike most, with the abdomen not being folded under the thorax. It comprises 46 extant species, and nearly 200 species known only from fossils.
Glypheidea is an infraorder of lobster-like decapod crustaceans, comprising a number of fossil forms and the two extant (living) genera Neoglyphea and Laurentaeglyphea: The infraorder was thought to be extinct until a living species, Neoglyphea inopinata, was discovered in 1975. They are now considered "living fossils", with over 256 fossil species discovered, and just two extant species.
Astacidae is a family of freshwater crayfish native to Europe and western North America. The family is made up of four extant (living) genera: The genera Astacus, Pontastacus, and Austropotamobius are all found throughout Europe and parts of western Asia, while Pacifastacus is found on the Pacific coast of the United States and British Columbia and includes the signal crayfish and the Shasta crayfish.
Thoracotremata is a clade of crabs, comprising those crabs in which the genital openings in both sexes are on the sternum, rather than on the legs. It comprises 17 families in four superfamilies .
Cyclodorippoida is a group of crabs, ranked as a section. It contains the single superfamily Cyclodorippoidea, which holds three families, Cyclodorippidae, Cymonomidae and Phyllotymolinidae.
Homoloidea is a superfamily of dromiacean crabs. Homoloidea belongs the group Dromiacea, taxonomically ranked as a section, and is the sister group to Dromioidea. Dromiacea is the most basal grouping of Brachyura crabs, and likely diverged from the rest of Brachyura around the Late Triassic or Early Jurassic. The close relation between Homoloidea and Dromioidea is primarily established through ultrastructural characteristics of the sperm.
Dromioidea is a superfamily of crabs mostly found in Madagascar. Dromioidea belongs the group Dromiacea, taxonomically ranked as a section, which is the most basal grouping of Brachyura crabs. Dromiacea likely diverged from the rest of Brachyura around the Late Triassic or Early Jurassic, and the earliest fossils attributable to the Dromioidea date from the Late Jurassic.
Podotremata is a traditionally used section of crabs (Brachyura), now considered to be invalid. It was the smaller grouping of crabs, separate from the larger Eubrachyura section. Morphological and molecular analyses do not reveal a monophyletic Podotremata, but rather that it is paraphyletic, and so the most recent classifications divide "Podotremata" into three sections: Dromiacea, Cyclodorippoidea and Raninoida.
Dromiacea is a group of crabs, ranked as a section. It contains 240 extant and nearly 300 extinct species. Dromiacea is the most basal grouping of Brachyura crabs, diverging the earliest in the evolutionary history, around the Late Triassic or Early Jurassic. Below is a cladogram showing Dromiacea's placement within Brachyura:
Polychelida is an infraorder of decapod crustaceans. Fossil representatives are known dating from as far back as the Upper Triassic. A total of 38 extant species, all in the family Polychelidae, and 55 fossil species have been described.
Eubrachyura is a group of decapod crustaceans comprising the more derived crabs. It is divided into two subsections, based on the position of the genital openings in the two sexes. In the Heterotremata, the openings are on the legs in the males, but on the sternum in females, while in the Thoracotremata, the openings are on the sternum in both sexes. This contrasts with the situation in other decapods, in which the genital openings are always on the legs. Heterotremata is the larger of the two groups, containing the species-rich superfamilies Xanthoidea and Pilumnoidea and all the freshwater crabs. The eubrachyura is well known for actively and constantly building its own burrows. The fossil record of the Eubrachyura extends back to the Cretaceous; the supposed Bathonian representative of the group, Hebertides jurassica, ultimately turned out to be Cenozoic in age.
Heterotremata is a clade of crabs, comprising those crabs in which the genital openings are on the sternum in females, but on the legs in males. It comprises 68 families in 28 superfamilies.
Gebiidea is an infraorder of decapod crustaceans. Gebiidea and Axiidea are divergent infraoders of the former infraorder Thalassinidea. These infraorders have converged ecologically and morphologically as burrowing forms. Based on molecular evidence as of 2009, it is now widely believed that these two infraorders represent two distinct lineages separate from one another. Since this is a recent change, much of the literature and research surrounding these infraorders still refers to the Axiidea and Gebiidea in combination as "thalassinidean" for the sake of clarity and reference. This division based on molecular evidence is consistent with the groupings proposed by Robert Gurney in 1938 based on larval developmental stages.
