Stalked spermatophore
of a collembolan
The Hexapods
Judging from the fossil record, hexapods must have diverged from myriapodan stock during the late Ordovician or early Silurian periods (400-500 million years ago). At this time in geological history, land masses were dotted with shallow inland seas, and plant life (mostly algae and bryophytes) was largely restricted to coastal habitats and other sites where water was readily available. The oldest hexapod fossils are found in rocks of the late Devonian period. These rocks also contain numerous other terrestrial arthropods (mites, spiders, centipedes, scorpions, etc.) suggesting that a major radiation of terrestrial life-forms must have occurred during the Ordovician or Silurian period.
At one time, all six-legged arthropods were considered "insects". It was a simple and elegant arrangement -- you just counted legs! But as we continue to learn more about these fascinating creatures, it has become increasingly difficult to justify grouping all "six-leggers" in a single class. There are major differences in external structures, organ systems, and post-embryonic development that seemingly point to evolutionary divergence between the "true" insects and three other closely allied groups: Protura, Diplura, and Collembola. Many entomologists still consider these three taxa to be "primitive" orders of insects, others prefer to classify them as orders in a separate class (the Entognatha), and still others insist that differences outnumber similarities and regard each taxon as a separate class of arthropods. This is the perennial debate between "splitters" and "lumpers". The controversy is not new and it will not be settled quickly. In this textbook, we have chosen to recognize Protura, Diplura, Collembola, and Insecta as four separate classes of hexapods, but we will accord the non-insect classes equal emphasis and parallel treatment to each of the orders within the class Insecta. Obviously, we want to have our cake, and eat it too!
Structurally and ecologically, the non-insect hexapods bear a close resemblance to myriapods. All members of these taxa exhibit ametabolous development (egg, young, adult); the proturans gain one abdominal segment during each of the first three molts (anamorphosis). Like myriapods, the Protura, Diplura, and Collembola are restricted to moist environments because their exoskeletons lack a protective layer of wax that seals, waterproofs, and minimizes desiccation. Their thin body wall also permits gas exchange with the
environment and serves as an important respiratory organ (some protura lack a tracheal system). During a molt, the exoskeleton of protura and collembola splits transversely behind the head (like millipedes and centipedes), rather than longitudinally along the back (as in the Insecta).
Protura have no antennae, but Diplura and Collembola have well-developed, multisegmented antennae. As in myriapods, the entire length of the antenna is musculated -- every segment is equipped with individual muscles, and every segment is independently capable of movement. Most evolutionary biologists regard this as a "primitive" state (pleisiomorphic condition) because all other six-legged arthropods (the true Insecta) have muscles in only the scape and pedicel, the two basal segments of the antennae.
External fertilization is another pleisiomorphic character that non-insect hexapods share with myriapods. In all of these groups, the sexes are separate (dioecious) but direct insemination of the female (copulation) does not occur. Instead, the male produces packets of sperm (spermatophores) that he sets on the ground or other substrate to be picked up by passing females. In general, spermatophores are deposited randomly in the environment and left for chance discovery by a receptive female. In some species, the males deposit spermatophores only in the vicinity of a prospective mate.
The most distinguishing characteristic of Protura, Diplura, and Collembola, and the one feature that sets them apart from all insects and myriapods, is the way their mouthparts are enclosed within the head capsule. This condition probably evolved through fusion of the labium and lateral head sclerites (hardened plates of the exoskeleton) along the lower portion of the head capsule. The mouthparts, therefore, are enclosed in a cavity that opens anteriorly. Food may be drawn into this cavity by suction and then chopped or ground by action of the mandibles and maxillae. Mouthparts enclosed within such a cavity are said to be entognathous, a term that is derived from the Greek "ento-" meaning inner and "gnathos" meaning jaw. All of the "true" insects are ectognathous: their mouthparts extend outside the head capsule.
