Chelicerata
The subphylum Chelicerata constitutes one of the major subdivisions of the phylum Arthropoda. Chelicerates include the sea spiders, horseshoe crabs, and arachnids, as well as a number of extinct lineages, such as the eurypterids and chasmataspidids.
Chelicerata split from Mandibulata by the mid-Cambrian, as evidenced by stem-group chelicerates like Habeliida and Mollisonia present by this time. The surviving marine species include the four species of xiphosurans, and possibly the 1,300 species of pycnogonids, if the latter are indeed chelicerates. On the other hand, there are over 77,000 well-identified species of air-breathing chelicerates, and there may be about 500,000 unidentified species.
Like all arthropods, chelicerates have segmented bodies with jointed limbs, all covered in a cuticle made of chitin and proteins. The chelicerate body plan consists of two tagmata, the prosoma and the opisthosoma – excepting the mites, which have lost any visible division between these sections. The chelicerae, which give the group its name, are the only appendages that appear before the mouth. In most sub-groups, they are modest pincers used to feed. However, spiders' chelicerae form fangs that most species use to inject venom into prey. The group has the open circulatory system typical of arthropods, in which a tube-like heart pumps blood through the hemocoel, which is the major body cavity. Marine chelicerates have gills, while the air-breathing forms generally have both book lungs and tracheae. In general, the ganglia of living chelicerates' central nervous systems fuse into large masses in the cephalothorax, but there are wide variations and this fusion is very limited in the Mesothelae, which are regarded the sister group to all other spiders. Most chelicerates rely on modified bristles for touch and for information about vibrations, air currents, and chemical changes in their environment. The most active hunting spiders also have very acute eyesight.
Chelicerates were originally predators, but the group has diversified to use all the major feeding strategies: predation, parasitism, herbivory, scavenging and eating decaying organic matter. Although harvestmen can digest solid food, the guts of most modern chelicerates are too narrow for this, and they generally liquidize their food by grinding it with their chelicerae and pedipalps and flooding it with digestive enzymes. To conserve water, air-breathing chelicerates excrete waste as solids that are removed from their blood by Malpighian tubules, structures that also evolved independently in insects.
While the marine horseshoe crabs rely on external fertilization, air-breathing chelicerates use internal but usually indirect fertilization. Many species use elaborate courtship rituals to attract mates. Most lay eggs that hatch as what look like miniature adults, but all scorpions and a few species of mites keep the eggs inside their bodies until the young emerge. In most chelicerate species the young have to fend for themselves, but in scorpions and some species of spider the females protect and feed their young.
The evolutionary origins of chelicerates from the early arthropods have been debated for decades. Although there is considerable agreement about the relationships between most chelicerate sub-groups, the inclusion of the Pycnogonida in this taxon has been questioned, and the exact position of scorpions is still controversial, though they were long considered the most sister to all other arachnids.
Venom has evolved three times in the chelicerates; spiders, scorpions and pseudoscorpions, or four times if the hematophagous secretions produced by ticks are included. In addition there have been unverified descriptions of venom glands in Solifugae. Chemical defense has been found in whip scorpions, shorttailed whipscorpions, harvestmen, beetle mites and sea spiders.
Although the venom of a few spider and scorpion species can be very dangerous to humans, medical researchers are investigating the use of these venoms for the treatment of disorders ranging from cancer to erectile dysfunction. The medical industry also uses the blood of horseshoe crabs as a test for the presence of contaminant bacteria. Mites can cause allergies in humans, transmit several diseases to humans and their livestock, and are serious agricultural pests.
Description
Segmentation and cuticle
The Chelicerata are arthropods as they have: segmented bodies with jointed limbs, all covered in a cuticle made of chitin and proteins; heads that are composed of several segments that fuse during the development of the embryo; a much reduced coelom; a hemocoel through which the blood circulates, driven by a tube-like heart. Chelicerates' bodies consist of two tagmata, sets of segments that serve similar functions: the foremost one, called the prosoma or cephalothorax, and the rear tagma is called the opisthosoma or abdomen. However, in the Acari there is no visible division between these sections.The prosoma is formed in the embryo by fusion of the ocular somite, which carries the eyes and labrum, with six post-ocular segments, which all have paired appendages. It was previously thought that chelicerates had lost the antennae-bearing somite 1, but later investigations reveal that it is retained and corresponds to a pair of chelicerae or chelifores, small appendages that often form pincers. Somite 2 has a pair of pedipalps that in most sub-groups perform sensory functions, while the remaining four cephalothorax segments have pairs of legs. In basal forms the ocular somite has a pair of compound eyes on the sides and four pigment-cup ocelli in the middle. The mouth is between somite 1 and 2.
The opisthosoma consists of thirteen or fewer segments, may or may not end with a telson. In some taxa such as scorpion and eurypterid the opisthosoma is divided into two groups, mesosoma and metasoma. The abdominal appendages of modern chelicerates are missing or heavily modified – for example in spiders the remaining appendages form spinnerets that extrude silk, while those of horseshoe crabs form gills.
Like all arthropods, chelicerates' bodies and appendages are covered with a tough cuticle made mainly of chitin and chemically hardened proteins. Since this cannot stretch, the animals must molt to grow. In other words, they grow new but still soft cuticles, then cast off the old one and wait for the new one to harden. Until the new cuticle hardens the animals are defenseless and almost immobilized.
Chelicerae and pedipalps
Chelicerae and pedipalps are the two pairs of appendages closest to the mouth; they vary widely in form and function and the consistent difference between them is their position in the embryo and corresponding neurons: chelicerae are deutocerebral and arise from somite 1, ahead of the mouth, while pedipalps are tritocerebral and arise from somite 2, behind the mouth.The chelicerae that give the sub-phylum its name normally consist of three sections, and the claw is formed by the third section and a rigid extension of the second. However, spiders' have only two sections, and the second forms a fang that folds away behind the first when not in use. The relative sizes of chelicerae vary widely: those of some fossil eurypterids and modern harvestmen form large claws that extended ahead of the body, while scorpions' are tiny pincers that are used in feeding and project only slightly in front of the head.
In some chelicerates, the pedipalps are unspecialized and subequal to the posterior pairs of walking legs. However, in sea spider and arachnids, the pedipalps are more or less specialized for sensory or prey-catching function – for example scorpions have pincers and male spiders have bulbous tips that act as syringes to inject sperm into the females' reproductive openings when mating.
Body cavities and circulatory systems
As in all arthropods, the chelicerate body has a very small coelom restricted to small areas round the reproductive and excretory systems. The main body cavity is a hemocoel that runs most of the length of the body and through which blood flows, driven by a tubular heart that collects blood from the rear and pumps it forward. Although arteries direct the blood to specific parts of the body, they have open ends rather than joining directly to veins, and chelicerates therefore have open circulatory systems as is typical for arthropods.Respiratory systems
These depend on individual sub-groups' environments. Modern terrestrial chelicerates generally have both book lungs, which deliver oxygen and remove waste gases via the blood, and tracheae, which do the same without using the blood as a transport system. The living horseshoe crabs are aquatic and have book gills that lie in a horizontal plane. For a long time it was assumed that the extinct eurypterids had gills, but the fossil evidence was ambiguous. However, a fossil of the long eurypterid Onychopterella, from the Late Ordovician period, has what appear to be four pairs of vertically oriented book gills whose internal structure is very similar to that of scorpions' book lungs.Feeding and digestion
The guts of most modern chelicerates are too narrow to take solid food. All scorpions and almost all spiders are predators that "pre-process" food in preoral cavities formed by the chelicerae and the bases of the pedipalps. However, one predominantly herbivore spider species is known, and many supplement their diets with nectar and pollen. Many of the Acari are blood-sucking parasites, but there are many predatory, herbivore and scavenger sub-groups. All the Acari have a retractable feeding assembly that consists of the chelicerae, pedipalps and parts of the exoskeleton, and which forms a preoral cavity for pre-processing food.Harvestmen are among the minority of living chelicerates that can take solid food, and the group includes predators, herbivores and scavengers. Horseshoe crabs are also capable of processing solid food, and use a distinctive feeding system. Claws at the tips of their legs grab small invertebrates and pass them to a food groove that runs from between the rearmost legs to the mouth, which is on the underside of the head and faces slightly backwards. The bases of the legs form toothed gnathobases that both grind the food and push it towards the mouth. This is how the earliest arthropods are thought to have fed.