Superfamily (taxonomy) in the context of "Crayfish"

Flea, the common name for the order Siphonaptera, includes 2,500 species of small flightless insects that live as external parasites of mammals and birds. Fleas live by ingesting the blood of their hosts. Adult fleas grow to about 3 millimetres (1⁄8 inch) long, are usually dark in color, and have bodies that are "flattened" sideways or narrow, enabling them to move through their hosts' fur or feathers. They lack wings; their hind legs are extremely well adapted for jumping. Their claws keep them from being dislodged, and their mouthparts are adapted for piercing skin and sucking blood. Some species can leap 50 times their body length, a feat second only to jumps made by another group of insects, the superfamily of froghoppers. Flea larvae are worm-like, with no limbs; they have chewing mouthparts and feed on organic debris left on their hosts' skin.

Genetic evidence indicates that fleas are a specialised lineage of parasitic scorpionflies (Mecoptera) sensu lato, most closely related to the family Nannochoristidae. The earliest known fleas lived in the Middle Jurassic; modern-looking forms appeared in the Cenozoic. Fleas probably originated on mammals first and expanded their reach to birds. Each species of flea specializes, more or less, on one species of host: many species of flea never breed on any other host; some are less selective. Some families of fleas are exclusive to a single host group; for example, the Malacopsyllidae are found only on armadillos, the Ischnopsyllidae only on bats, and the Chimaeropsyllidae only on elephant shrews.

Equidae (commonly known as the horse family) is the taxonomic family of horses and related animals, including asses, zebras, and many extinct species known only from fossils. The family evolved more than 50 million years ago, in the Eocene epoch, from a small, multi-toed ungulate into larger, single-toed animals. All extant species are in the genus Equus, which originated in North America. Equidae belongs to the order Perissodactyla, which includes the extant tapirs and rhinoceros, and several extinct families. It is more specifically grouped within the superfamily Equoidea, the only other family being the extinct Palaeotheriidae.

The term equid refers to any member of this family, including any equine.

Musteloidea is a superfamily of carnivoran mammals united by shared characteristics of the skull and teeth. Musteloids are the sister group of pinnipeds, the group which includes seals and allies.

Butterflies are winged insects from the lepidopteran superfamily Papilionoidea, characterised by large, often brightly coloured wings that often fold together when at rest, and a conspicuous, fluttering flight. The oldest butterfly fossils have been dated to the Paleocene, about 56 million years ago, though molecular evidence suggests that they likely originated in the Cretaceous.

Butterflies have a four-stage life cycle, and like other holometabolous insects they undergo complete metamorphosis. Winged adults lay eggs on plant foliage on which their larvae, known as caterpillars, will feed. The caterpillars grow, sometimes very rapidly, and when fully developed, pupate in a chrysalis. When metamorphosis is complete, the pupal skin splits, the adult insect climbs out, expands its wings to dry, and flies off.

Physeteroidea is a superfamily that includes three extant species of whales: the sperm whale, in the genus Physeter, and the pygmy sperm whale and dwarf sperm whale, in the genus Kogia. In the past, these genera have sometimes been united in a single family, the Physeteridae, with the two Kogia species in the subfamily Kogiinae; however, recent practice is to allocate the genus Kogia to its own family, the Kogiidae, leaving the Physeteridae as a monotypic (single extant species) family, although additional fossil representatives of both families are known.

Equoidea is a superfamily of hippomorph perissodactyls containing the Equidae, Palaeotheriidae, and other basal equoids of unclear affinities, of which members of the genus Equus are the only extant species. The earliest fossil record of the Equoidea proves unclear, but they possibly could have originated during the late Paleocene in Europe or Asia. Definite fossil records of equoids are recorded by the earliest Eocene, in which the earliest equids in North America and basal equoids of unclear affinities in Europe both appeared. Palaeotheres are thought to have originated later in the early Eocene of Europe, although some researchers disagree on whether the subfamily Pachynolophinae belongs to the Palaeotheriidae.

Equoids may in part be defined by dental synapomorphies from its molars. Equoids were originally brachyodont (low-crowned) in dentition, but the morphologies of their molars had changed to adapt to different diets. Living equids are hypsodont, the result of evolutionary adaptations towards grazing diets.

Hermit crabs are anomuran decapod crustaceans of the superfamily Paguroidea that have adapted to occupy empty scavenged gastropod shells to protect their fragile abdomens. There are over 800 species of hermit crab, most of which possess an asymmetric abdomen concealed by a snug-fitting shell. Hermit crabs' soft (non-calcified) abdominal exoskeleton means they must occupy shelter produced by other organisms or risk being defenseless.

The strong association between hermit crabs and their shelters has significantly influenced their biology. Almost 800 species carry mobile shelters (most often calcified snail shells); this protective mobility contributes to the diversity and multitude of these crustaceans which are found in almost all marine environments. In most species, development involves metamorphosis from symmetric, free-swimming larvae to morphologically asymmetric, benthic-dwelling, shell-seeking crabs. Such physiological and behavioral extremes facilitate a transition to a sheltered lifestyle, revealing the extensive evolutionary lengths that led to the superfamily's success.