Hypermetamorphosis should not be confused with Hypermorphosis.
Hypermetamorphosis, or heteromorphosis,[1] is a term used mainly in entomology; it refers to a class of variants of holometabolism, that is to say, complete insect metamorphosis. Hypermetamorphosis is exceptional in that some instars, usually larval instars, are functionally and visibly distinct from the rest. The differences between such instars usually reflect transient stages in the life cycle; for instance, one instar might be mobile while it searches for its food supply, while the following instar immediately sheds its locomotory organs and settles down to feed until it is fully grown and ready to change into the reproductive stage, which in turn, does not have the same nutritional requirements as the larvae.
Hypermetamorphosis, as the term normally is used in entomology, refers to a class of variants of holometabolism. In hypermetamorphosis some larval instars are functionally and morphologically distinct from each other. The general case in holometabolous insects such as flies, moths, or wasps, is that all larval stages look similar, growing larger as the insect matures. In hypermetamorphic insects however, at least one instar, usually the first, differs markedly from the rest. In many hypermetamorphic species, the first instars are numerous, tiny, very mobile larvae that must find their way to a food source. The general term for a mobile first instar is a planidium, from the Greek language πλάνος (planos) meaning "roaming".
In typical examples the first-instar larval morphology is campodeiform (meaning: elongated, flattened, and active, more or less resembling the morphology of insects in the genus Campodea). There is however, considerable variety in the forms of planidia that occur in various families and orders; in the beetle family Meloidae, the three-clawed planidium originally was called a triungulin, and similar planidia for example, those of the Strepsiptera, may also be called triungula.
In their planidial form, many species do not feed; they first change their skin and change their bodily form to a form suited to eating rather than seeking out food. The second instar is completely different in appearance and behavior, often becoming grub- or maggot-like in the instars before pupation. As a rule, the instars after the first ecdysis are of more or less constant form and not highly mobile, being specialised for feeding and growth until the final larval instar metamorphoses into the pupal form.[2]
The moth family Gracillariidae is an unusual case of hypermetamorphosis in that its first few larval instars do feed, but differently to later instars. Specifically, early instars feed on plant sap (and for this reason have modified mandibles) while later instars feed on plant tissue. Furthermore, instead of becoming less mobile during the larval stage, larvae become more mobile, with early instars lacking legs while later instars possess legs.[3]
There are examples of holometabolic species in which there are certain striking differences between the earliest instars and the later instars, though without their generally being regarded as hypermetamorphic. For example, early instars of many Papilionidae are of a colour, shape and texture that suggest bird droppings; later instars that are larger and would simply stand out in such camouflage, typically become green.[4] The prepupa or last larval instar of insects ceases to feed and (in some cases) searches for a place to pupate,[5] [6] but this also is not considered hypermetamorphosis.
Hypermetamorphosis usually occurs as an adaptation of the ontogeny of certain parasitoid insects, notably:
Technically, the subimago of the Ephemeroptera might be described as a stage in a form of hypermetamorphosis, but that is not common practice.[7]
Examples of hypermetamorphosis in any given insect order are analogous and not homologous to those in any other order; for example, hypermetamorphosis in the Acroceridae was not derived from the Strepsiptera.