8.7 Superphylum Ecdysozoa: Arthropods

Morphology

Characteristic features of the arthropods include the presence of jointed appendages, body segmentation, and chitinized exoskeleton. Fusion of adjacent groups of segments gave rise to functional body regions called tagmata (singular = tagma). Tagmata may be in the form of a head, thorax, and abdomen, or a cephalothorax and abdomen, or a head and trunk, depending on the taxon. Commonly described tagmata may be composed of different numbers of segments; for example, the head of most insects results from the fusion of six ancestral segments, whereas the “head” of another arthropod may be made of fewer ancestral segments, due to independent evolutionary events. Jointed arthropod appendages, often in segmental pairs, have been specialized for various functions: sensing their environment (antennae), capturing and manipulating food (mandibles and maxillae), as well as for walking, jumping, digging, and swimming.

In the arthropod body, a central cavity, called the hemocoel (or blood cavity), is present, and the hemocoel fluids are moved by contraction of regions of the tubular dorsal blood vessel called “hearts.” Groups of arthropods also differ in the organs used for nitrogenous waste excretion, with crustaceans possessing green glands and insects using Malpighian tubules, which work in conjunction with the hindgut to reabsorb water while ridding the body of nitrogenous waste. The nervous system tends to be distributed among the segments, with larger ganglia in segments with sensory structures or appendages. The ganglia are connected by a ventral nerve cord.

Respiratory systems vary depending on the group of arthropods. Insects and myriapods use a series of tubes (tracheae) that branch through the body, ending in minute tracheoles. These fine respiratory tubes perform gas exchange directly between the air and cells within the organism. The major tracheae open to the surface of the cuticle via apertures called spiracles. We should note that these tracheal systems of ventilation have evolved independently in hexapods, myriapods, and arachnids. Although the tracheal system works extremely well in terrestrial environments, it also works well in freshwater aquatic environments. In fact, numerous species of aquatic insects in both immature and adult stages possess tracheal systems. However, although there are insects that live on the surface of marine environments, none is strictly marine—meaning that they complete their entire metamorphosis in salt water.

In contrast, aquatic crustaceans utilize gills, terrestrial chelicerates employ book lungs, and aquatic chelicerates use book gills (see figure below). The book lungs of arachnids (scorpions, spiders, ticks, and mites) contain a vertical stack of hemocoel wall tissue that somewhat resembles the pages of a book. Between each of the “pages” of tissue is an air space. This allows both sides of the tissue to be in contact with the air at all times, greatly increasing the efficiency of gas exchange. The gills of crustaceans are filamentous structures that exchange gases with the surrounding water.

The cuticle is the hard “covering” of an arthropod. It is made up of two layers: the epicuticle, which is a thin, waxy, water-resistant outer layer containing no chitin, and the layer beneath it, the chitinous procuticle, which itself is composed of an exocuticle and a lower endocuticle, all supported ultimately by a basement membrane. The exoskeleton is very protective (it is sometimes difficult to squish a big beetle!), but does not sacrifice flexibility or mobility. Both the exocuticle (which is secreted before a molt) and an endocuticle (which is secreted after a molt) are composed of chitin bound with a protein; chitin is insoluble in water, alkalis, and weak acids. The procuticle is not only flexible and lightweight, but also provides protection against dehydration and other biological and physical stresses. Some hexapods, such as the crustaceans, add calcium salts to their exoskeleton, which increases the strength of the cuticle, but does reduce its flexibility. In some cases, such as lobsters, the amount of calcium salt deposited within the chitin is extreme. In order to grow, the arthropod must “shed” the exoskeleton during the physiological process called molting, following by the actual stripping of the outer cuticle, called ecdysis (“to strip off”). At first, this seems to be a dangerous method of growth, because while the new exoskeleton is hardening, the animal is vulnerable to predation; however, molting and ecdysis also allow for growth and change in morphology, as well as for great diversification in size, simply because the numbers of molts can be modified through evolution.

Subphylum Chelicerata

This subphylum includes animals such as horseshoe crabs, sea spiders, spiders, mites, ticks, scorpions, whip scorpions (see figure below), and harvestmen. Chelicerates are predominantly terrestrial, although some freshwater and marine species also exist. An estimated 77,000 species of chelicerates can be found in almost all terrestrial habitats.

The body of chelicerates is divided into two tagmata: prosoma and opisthosoma, which are basically the equivalents of a cephalothorax (usually smaller) and an abdomen (usually larger). A distinct “head” tagma is not usually discernible. The phylum derives its name from the first pair of appendages: the chelicerae, which serve as specialized clawlike or fanglike mouthparts. We should note here that chelicerae are actually modified legs, but they are not the exact serial equivalent of mandibles, which are the modified leglike chewing mouthparts of insects and crustaceans: The chelicerae are borne on the first segment making up the prosoma, whereas the mandibles are embryonically on the fourth segment of the mandibulate head. The chelicerates have secondarily lost their antennae and hence do not have them. Some of the functions of the antennae (such as touch) are now performed by the second pair of appendages— the pedipalps, which may also be used for general sensing the environment as well as the manipulation of food. In some species, such as sea spiders, an additional pair of derived leg appendages, called ovigers, is present between the chelicerae and pedipalps. Ovigers are used for grooming and by males to carry eggs. In spiders, the chelicerae are often modified and terminate in fangs that inject venom into their prey before feeding.

 

Most chelicerates ingest food using a preoral cavity formed by the chelicerae and pedipalps. Some chelicerates may secrete digestive enzymes to pre-digest food before ingesting it. Parasitic chelicerates like ticks and mites have evolved blood-sucking apparatuses. Members of this subphylum have an open circulatory system with a heart that pumps blood into the hemocoel. Aquatic species, like horseshoe crabs, have gills, whereas terrestrial species have either tracheae or book lungs for gaseous exchange. Chelicerate hemolymph contains hemocyanin a copper-containing oxygen transport protein.

The nervous system in chelicerates consists of a brain and two ventral nerve cords. Chelicerates are dioecious, meaning that the sexes are separate. These animals use external fertilization as well as internal fertilization strategies for reproduction, depending upon the species and its habitat. Parental care for the young ranges from absolutely none to relatively prolonged care.

Subphylum Myriapoda comprises arthropods with numerous legs (see figure below). Although the name is misleading, suggesting that thousands of legs are present in these invertebrates, the number of legs typically varies from 10 to 750. This subphylum includes 16,000 species; the most commonly found examples are millipedes and centipedes. Virtually all myriapods are terrestrial animals and prefer a humid environment. Ancient myriapods (or myriapod-like arthropods) from the Silurian to the Devonian grew up to 10 feet in length (three meters). Unfortunately, they are all extinct!

Myriapods are typically found in moist soils, decaying biological material, and leaf litter. Subphylum Myriapoda is divided into four classes: Chilopoda, Symphyla, Diplopoda, and Pauropoda. Centipedes like Scutigera coleoptrata are classified as chilopods. These animals bear one pair of legs per segment, mandibles as mouthparts, and are somewhat dorsoventrally flattened. The legs in the first segment are modified to form forcipules (poison claws) that deliver poison to prey like spiders and cockroaches, as these animals are all predatory. Symphyla are similar to centipedes but lack the poison claws and are vegetarian. Millipedes bear two pairs of legs per diplosegment—a feature that results from the embryonic fusion of adjacent pairs of body segments. These arthropods are usually rounder in cross-section than centipedes, and are herbivores or detritivores. Millipedes have visibly more numbers of legs as compared to centipedes, although they do not have a thousand legs. The Pauropods are similar to millipedes, but have fewer segments.

Subphylum Crustacea

Crustaceans are the most dominant aquatic (both freshwater and marine) arthropods, with the total number of marine crustaceans standing at about 70,000 species. Krill, shrimp, lobsters, crabs, and crayfish are examples of crustaceans (see figure below). However, there are also a number of terrestrial crustacean species as well: Terrestrial species like the wood lice (Armadillidium spp.), also called pill bugs, roly-polies, potato bugs, or isopods, are also crustaceans. Nonetheless, the number of terrestrial species in this subphylum is relatively low.

Crustaceans typically possess two pairs of antennae, mandibles as mouthparts, and biramous (“two branched”) appendages, which means that their legs are formed in two parts called endopods and exopods, which appear superficially distinct from the uniramous (“one branched”) legs of myriapods and hexapods (see figure below). Since biramous appendages are also seen in the trilobites, biramous appendages represent the ancestral condition in the arthropods. Currently, we describe various arthropods as having uniramous or biramous appendages, but these are descriptive only, and do not necessarily reflect evolutionary relationships other than that all jointed legs of arthropods share common ancestry.

In most crustaceans, the head and thorax are fused to form a cephalothorax, which is covered by a plate called the carapace, thus producing a body plan comprising two tagmata: cephalophorax and abdomen. Crustaceans have a chitinous exoskeleton that is shed by molting and ecdysis whenever the animal requires an increase in size or the next stage of development. The exoskeletons of many aquatic species are also infused with calcium carbonate, which makes them even stronger than those of other arthropods. Crustaceans have an open circulatory system where blood is pumped into the hemocoel by the dorsally located heart (see figure below). Hemocyanin is the major respiratory pigment present in crustaceans, but hemoglobin is found in a few species and both are dissolved in the hemolymph rather than carried in cells.

As in the chelicerates, most crustaceans are dioecious. However, some species like barnacles may be hermaphrodites. Serial hermaphroditism, where the gonad can switch from producing sperm to ova, is also exhibited in some species. Fertilized eggs may be held within the female of the species or may be released in the water. Terrestrial crustaceans seek out damp spaces in their habitats to lay eggs.

Crustaceans possess a brain formed by the fusion of the first three segmental ganglia, as well as two compound eyes. A ventral nerve cord connects additional segmental ganglia. Most crustaceans are carnivorous, but herbivorous and detritivorous species, and even endoparasitic species are known. A highly evolved endoparasitic species, such as Sacculina spp., parasitizes its crab host and ultimately destroys it after it forces the host to incubate the parasite’s eggs! Crustaceans may also be cannibalistic when extremely high populations of these organisms are present.

Subphylum Hexapoda

The insects comprise the largest class of arthropods in terms of species diversity as well as in terms of biomass—at least in terrestrial habitats.

The name Hexapoda describes the presence of six legs (three pairs) in these animals, which differentiates them from other groups of arthropods that have different numbers of legs. In some cases, however, the number of legs has been evolutionarily reduced, or the legs have been highly modified to accommodate specific conditions, such as endoparasitism. Hexapod bodies are organized into three tagmata: head, thorax, and abdomen. Individual segments of the head have mouthparts derived from jointed legs, and the thorax has three pairs of jointed appendages, and also wings, in most derived groups. For example, in the pterygotes (winged insects), in addition to a pair of jointed legs on all three segments comprising the thorax: prothorax, mesothorax, and metathorax (see figure below).

Appendages found on other body segments are also evolutionarily derived from modified legs. Typically, the head bears an upper “lip” or labrum and mandibles (or derivation of mandibles) that serve as mouthparts; maxillae, and a lower “lip” called a labium: both of which manipulate food. The head also has one pair of sensory antennae, as well as sensory organs such as a pair of compound eyes, ocelli (simple eyes), and numerous sensory hairs. The abdomen usually has 11 segments and bears external reproductive apertures. The subphylum Hexapoda includes some insects that are winged (such as fruit flies) and others that are secondarily wingless (such as fleas). The only order of “primitively wingless” insects is the Thysanura, the bristletails. All other orders are winged or are descendants of formally winged insects.

The evolution of wings is a major, unsolved mystery. Unlike vertebrates, whose “wings” are simply preadaptations of “arms” that served as the structural foundations for the evolution of functional wings (this has occurred independently in pterosaurs, dinosaurs [birds], and bats), the evolution of wings in insects is a what we call a de novo (new) development that has given the pteryogotes domination over the Earth. Winged insects existed over 425 million years ago, and by the Carboniferous, several orders of winged insects (Paleoptera), most of which are now extinct, had evolved. There is good physical evidence that Paleozoic nymphs with thoracic winglets (perhaps hinged, former gill covers of semi-aquatic species) used these devices on land to elevate the thoracic temperature (the thorax is where the legs are located) to levels that would enable them to escape predators faster, find more food resources and mates, and disperse more easily. The thoracic winglets (which can be found on fossilized insects preceding the advent of truly winged insects) could have easily been selected for thermoregulatory purposes prior to reaching a size that would have allowed them the capacity for gliding or actual flapping flight. Even modern insects with broadly attached wings, such as butterflies, use the basal one-third of their wings (the area next to the thorax) for thermoregulation, and the outer two-thirds for flight, camouflage, and mate selection.

Many of the common insects we encounter on a daily basis—including ants, beetles, cockroaches, butterflies, crickets and flies—are examples of Hexapoda. Among these, adult ants, beetles, flies, and butterflies develop by complete metamorphosis from grub-like or caterpillar-like larvae, whereas adult cockroaches and crickets develop through a gradual or incomplete metamorphosis from wingless immatures. All growth occurs during the juvenile stages. Adults do not grow further (but may become larger) after their final molt. Variations in wing, leg, and mouthpart morphology all contribute to the enormous variety seen in the insects. Insect variability was also encouraged by their activity as pollinators and their coevolution with flowering plants. Some insects, especially termites, ants, bees, and wasps, are eusocial, meaning that they live in large groups with individuals assigned to specific roles or castes, like queen, drone, and worker. Social insects use pheromones—external chemical signals—to communicate and maintain group structure as well as a cohesive colony.