caterpillar, larva of a butterfly or moth (Lepidoptera). Most caterpillars have cylindrical bodies consisting of multiple segments, with three pairs of true legs on the thorax and several pairs of short, fleshy prolegs on the abdomen. The head has six small eyes (stemmata) on each side that function in light detection but not in image formation. They have short segmented antennae and strong jaws. Many caterpillars within the order Lepidoptera are called worms, such as the measuring worm, silkworm, and armyworm.

Caterpillars are known for their voracious appetites. They generally eat leaves of various types of plants, though some species eat insects or other small animals. Leaf-eating species can cause extensive damage to fruit trees, crops, ornamental plants, hardwood trees, and shrubs. For example, caterpillars of the cabbage looper moth (Trichoplusia ni) can consume three times their body weight in leaf matter daily. In addition to the damage these caterpillars cause by eating the leaves of cabbages and allied crops, the fecal matter they produce, known as frass, can stain leaves and render the plants unsaleable. Examples of insect-eating caterpillars include those of harvester butterflies (Feniseca tarquinius), which prey on woolly aphids, and the butterfly Alesa amesis, which feeds on the nymphs of insects in the order Homoptera. The snail-eating Hyposmocoma molluscivora is the only lepidopteran known to feed on a type of gastropod.

Some caterpillars possess specialized underwater respiratory structures that enable them to survive in aquatic habitats. For example, the larvae of some pyralid moths (family Pyralidae) are aquatic, and several members of the genus Hyposmocoma (family Cosmopterigidae) have an amphibious caterpillar stage. Some caterpillars spin silk cases, which provide protective shelters. These cases often have leaves, pebbles, and other matter woven into them, thereby making the caterpillars appear as part of their natural surroundings. Some examples of case-making caterpillars include larvae of the Asian hydrilla moth (Parapoynx diminutalis) and larvae of Hyposmocoma.

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The appearance of caterpillars is highly variable, particularly concerning their coloration, which plays a fundamental role in their ability to protect themselves from predators. In many instances, a caterpillar’s appearance is meant to imitate that of its surroundings, and it changes as the larva grows. For example, young larvae of many swallowtail butterflies (Papilio) are white and brown and resemble bird droppings on leaves, but, as the caterpillars grow, their appearance changes such that their colours eventually serve as camouflage enabling them to blend in with the leaves and stems of plants. In some caterpillars, coloration is conspicuous or is augmented by the presence of features such as false eyespots, which may serve to deceive or frighten predators.

Other defense strategies used by caterpillars include the release of foul-smelling chemicals, the production of noises such as chirps, the generation of vibratory signals, and the sequestration in tissues of chemicals toxic to predators. Caterpillars of the giant peacock moth (Saturnia pyri) send out ultrasonic warning chirps to deter predators. In some cases, those chirps occur just prior to or in conjunction with the release of pungent chemical deterrents. The masked birch caterpillar (Drepana arcuata) produces vibratory signals in order to defend its territory against intruders of the same species; it produces the vibrations by drumming its mandibles on the leaf surface and by scratching its legs, which are covered by hairlike structures, against the leaf. Larvae of monarch butterflies (Danaus plexippus) rely on a system of defense associated with their unique ability to feed on milkweed plants (Asclepias). These plants produce compounds known as cardenolides, which are normally toxic to animals. Monarch larvae, however, are unaffected by the poison, and they are able to sequester the compound in their tissues. Because the poison stays with the insects as they mature through subsequent stages of development, they are toxic to vertebrate predators both as larvae and as adult butterflies.

Caterpillar-like, or eruciform, larvae also occur in other insect groups, namely the scorpionflies (Mecoptera) and the sawflies (Hymenoptera). These can be distinguished in that most Lepidoptera caterpillars have prolegs on segments 3 through 6 and 10 of the abdomen, although this number may be reduced. In Mecoptera, prolegs are present on segments 1 to 8, and segment 10 has either a pair of hooks or a suction disk. Sawfly larvae have prolegs on all abdominal segments.

The Editors of Encyclopaedia Britannica This article was most recently revised and updated by Adam Augustyn.

pollination, transfer of pollen grains from the stamens (the flower parts that produce them) to the ovule-bearing organs or to the ovules (seed precursors) themselves. In gymnosperm plants such as conifers and cycads, in which the ovules are exposed, the pollen is simply caught in a drop of fluid secreted by the ovule. In flowering plants, however, the ovules are contained within a hollow organ called the pistil, and the pollen is deposited on the pistil’s receptive surface, the stigma. There the pollen germinates and gives rise to a pollen tube, which grows down through the pistil toward one of the ovules in its base. In an act of double fertilization, one of the two sperm cells within the pollen tube fuses with the egg cell of the ovule, making possible the development of an embryo, and the other cell combines with the two subsidiary sexual nuclei of the ovule, which initiates formation of a reserve food tissue, the endosperm. The growing ovule then transforms itself into a seed.

As a prerequisite for fertilization, pollination is essential to the perpetuation of the vast majority of the world’s wild plants as well as to the production of most fruit and seed crops. It also plays an important part in programs designed to improve plants by breeding. Furthermore, studies of pollination are invaluable for understanding the evolution of flowering plants and their distribution in the world today. As sedentary organisms, plants usually must enlist the services of external agents for pollen transport. In flowering plants, these are (roughly in order of diminishing importance) insects, wind, birds, mammals, and water. See also major types of pollinators.

Types: self-pollination and cross-pollination

An egg cell in an ovule of a flower may be fertilized by a sperm cell derived from a pollen grain produced by that same flower or by another flower on the same plant, in either of which two cases fertilization is said to be due to self-pollination (autogamy); or, the sperm may be derived from pollen originating on a different plant individual, in which case the process is called cross-pollination (heterogamy). Both processes are common, but cross-pollination clearly has certain evolutionary advantages for the species: the seeds formed may combine the hereditary traits of both parents, and the resulting offspring generally are more varied than would be the case after self-pollination. In a changing environment, some of the individuals resulting from cross-pollination still may be found capable of coping with their new situation, ensuring survival of the species, whereas the individuals resulting from self-pollination might all be unable to adjust. Self-pollination, or selfing, although foolproof in a stable environment, thus is an evolutionary cul-de-sac. There also is a more direct, visible difference between selfing and outbreeding (cross-pollination): in those species where both methods work, cross-pollination usually produces more, and better quality, seeds. A dramatic demonstration of this effect is found with hybrid corn (maize), a superior product that results from cross-breeding of several especially bred lines.