Adult arachnids have eight
legs attached to the
cephalothorax, although the frontmost pair of legs in some species has converted to a sensory function, while in other species, different
appendages can grow large enough to take on the appearance of extra pairs of legs. The term is derived from the
Greek word ἀράχνη (aráchnē, 'spider'), from the myth of the hubristic human weaver
Arachne, who was turned into a spider.[2]
Almost all
extant arachnids are
terrestrial, living mainly on land. However, some inhabit freshwater environments and, with the exception of the
pelagic zone, marine environments as well. They comprise over 110,000 named
species, of which 51,000 are species of spiders.[3][4]
Morphology
Almost all adult arachnids have eight legs, unlike adult
insects which all have six legs. However, arachnids also have two further pairs of appendages that have become adapted for feeding, defense, and sensory perception. The first pair, the
chelicerae, serve in feeding and defense. The next pair of appendages, the
pedipalps, have been adapted for feeding, locomotion, and/or
reproductive functions. In scorpions, pseudoscorpions, and ricinuleids the pedipalps ends in a pair of pinchers, and in whip scorpions, Schizomida, Amblypygi, and most harvestmen, they are
raptorial and used for prey capture.[5] In
Solifugae, the palps are quite leg-like, so that these animals appear to have ten legs. The
larvae of mites and
Ricinulei have only six legs; a fourth pair usually appears when they
moult into
nymphs. However, mites are variable: as well as eight, there are adult mites with six or, like in
Eriophyoidea, even four legs.[6][7] And while the adult males in some members of Podapolipidae have six legs, the adult females have only a single pair.[8]
Arachnids are further distinguished from insects by the fact they do not have
antennae or
wings. Their body is organized into two
tagmata, called the
prosoma, or
cephalothorax, and the
opisthosoma, or
abdomen. (However, there is currently neither fossil nor embryological evidence that arachnids ever had a separate thorax-like division, so the validity of the term cephalothorax, which means a fused
cephalon, or head, and
thorax, has been questioned. There are also arguments against use of 'abdomen', as the opisthosoma of many arachnids contains organs atypical of an abdomen, such as a heart and respiratory organs.[9]) The prosoma, or cephalothorax, is usually covered by a single, unsegmented carapace. The abdomen is segmented in the more primitive forms, but varying degrees of fusion between the segments occur in many groups. It is typically divided into a preabdomen and postabdomen, although this is only clearly visible in scorpions, and in some orders, such as the
Acari, the abdominal sections are completely fused.[10] A
telson is present in scorpions, where it has been modified to a stinger, and into a flagellum in the Palpigradi, Schizomida (very short) and
whip scorpions.[11] At the base of the flagellum in the two latter groups there are gland who produce acetic acid as a chemical defense.[12] Except for a pair of pectines in scorpions,[13] and the spinnerets in spiders, the abdomen has no appendages.[14]
Like all arthropods, arachnids have an
exoskeleton, and they also have an internal structure of
cartilage-like tissue, called the
endosternite, to which certain muscle groups are attached. The endosternite is even calcified in some
Opiliones.[15]
Most arachnids lack
extensor muscles in the
distal joints of their appendages. Spiders and
whipscorpions extend their limbs hydraulically using the pressure of their
hemolymph.[16]Solifuges and some
harvestmen extend their knees by the use of highly elastic thickenings in the joint cuticle.[16]Scorpions,
pseudoscorpions and some harvestmen have evolved muscles that extend two leg joints (the femur-patella and patella-tibia joints) at once.[17][18] The equivalent joints of the pedipalps of scorpions though, are extended by elastic recoil.[19]
There are characteristics that are particularly important for the terrestrial lifestyle of arachnids, such as internal respiratory surfaces in the form of
tracheae, or modification of the
book gill into a
book lung, an internal series of
vascularlamellae used for
gas exchange with the air.[20] While the tracheae are often individual systems of tubes, similar to those in insects, ricinuleids, pseudoscorpions, and some spiders possess sieve tracheae, in which several tubes arise in a bundle from a small chamber connected to the
spiracle. This type of tracheal system has almost certainly evolved from the book lungs, and indicates that the tracheae of arachnids are not
homologous with those of insects.[21]
Further adaptations to terrestrial life are
appendages modified for more efficient locomotion on land, internal fertilisation, special sensory organs, and water conservation enhanced by efficient
excretory structures as well as a waxy layer covering the cuticle.
The excretory glands of arachnids include up to four pairs of
coxal glands along the side of the prosoma, and one or two pairs of
Malpighian tubules, emptying into the gut. Many arachnids have only one or the other type of excretory gland, although several do have both. The primary nitrogenous waste product in arachnids is
guanine.[21]
Arachnid blood is variable in composition, depending on the mode of respiration. Arachnids with an efficient tracheal system do not need to transport oxygen in the blood, and may have a reduced circulatory system. In scorpions and some spiders, however, the blood contains
haemocyanin, a copper-based pigment with a similar function to
haemoglobin in vertebrates. The
heart is located in the forward part of the abdomen, and may or may not be segmented. Some mites have no heart at all.[21]
Diet and digestive system
Arachnids are mostly
carnivorous, feeding on the pre-digested bodies of insects and other small animals. But ticks, and many mites, are parasites, some of which are carriers of disease. The diet of
mites also include tiny animals, fungi, plant juices and decomposing matter.[22] Almost as varied is the diet of
harvestmen, where we will find predators, decomposers and omnivores feeding on decaying plant and animal matter, droppings, animals and mushrooms.[23][24][25] The
harvestmen and some mites, such as the
house dust mite, are also the only arachnids able to ingest solid food, which exposes them to internal parasites,[26] although it is not unusual for spiders to eat their own silk. And
one species of spider is mostly herbivorous.[27] Scorpions, spiders and pseudoscorpions secrete
venom from specialized
glands to kill prey or defend themselves.[28] Their venom also contains pre-digestive enzymes that helps breaking down the prey.[29][30][31] The saliva of ticks contains anticoagulants and anticomplements, and several species produce a
neurotoxin.[32][33]
Arachnids produce digestive enzymes in their stomachs, and use their pedipalps and chelicerae to pour them over their dead prey. The digestive juices rapidly turn the prey into a broth of nutrients, which the arachnid sucks into a pre-buccal cavity located immediately in front of the mouth. Behind the mouth is a muscular, sclerotised
pharynx, which acts as a pump, sucking the food through the mouth and on into the
oesophagus and
stomach. In some arachnids, the oesophagus also acts as an additional pump.
The stomach is tubular in shape, with multiple
diverticula extending throughout the body. The stomach and its diverticula both produce digestive enzymes and absorb nutrients from the food. It extends through most of the body, and connects to a short sclerotised
intestine and
anus in the hind part of the abdomen.[21]
Senses
Arachnids have two kinds of eyes: the lateral and median
ocelli. The lateral ocelli evolved from
compound eyes and may have a
tapetum, which enhances the ability to collect light. With the exception of scorpions, which can have up to five pairs of lateral ocelli, there are never more than three pairs present. The median ocelli develop from a transverse fold of the
ectoderm. The ancestors of modern arachnids probably had both types, but modern ones often lack one type or the other.[26] The
cornea of the eye also acts as a lens, and is continuous with the cuticle of the body. Beneath this is a transparent vitreous body, and then the
retina and, if present, the tapetum. In most arachnids, the retina probably does not have enough light sensitive cells to allow the eyes to form a proper image.[21]
In addition to the eyes, almost all arachnids have two other types of sensory organs. The most important to most arachnids are the fine sensory hairs that cover the body and give the animal its sense of touch. These can be relatively simple, but many arachnids also possess more complex structures, called
trichobothria.
Finally, slit sense organs are slit-like pits covered with a thin membrane. Inside the pit, a small hair touches the underside of the membrane, and detects its motion. Slit sense organs are believed to be involved in
proprioception, and possibly also hearing.[21]
Arachnids may have one or two
gonads, which are located in the abdomen. The genital opening is usually located on the underside of the second abdominal segment. In most species, the male transfers sperm to the female in a package, or
spermatophore. The males in harvestmen and some mites have a penis.[34] Complex courtship rituals have evolved in many arachnids to ensure the safe delivery of the sperm to the female.[21] Members of many orders exhibit sexual dimorphism.[35]
Arachnids usually lay yolky
eggs, which hatch into immatures that resemble adults. Scorpions, however, are either
ovoviviparous or
viviparous, depending on species, and bear live young. Also some mites are ovoviviparous and viviparous, even if most lay eggs.[36] In most arachnids only the females provide parental care, with harvestmen being one of the few exceptions.[37][38]
Taxonomy and evolution
Phylogeny
The
phylogenetic relationships among the main subdivisions of arthropods have been the subject of considerable research and dispute for many years. A consensus emerged from about 2010 onwards, based on both morphological and molecular evidence; extant (living) arthropods are a
monophyletic group and are divided into three main clades: chelicerates (including arachnids), pancrustaceans (the
paraphyletic crustaceans plus insects and their allies), and myriapods (centipedes, millipedes and allies).[39][40][41][42][43] The three groups are related as shown in the
cladogram below.[41] Including fossil taxa does not fundamentally alter this view, although it introduces some additional basal groups.[44]
The extant chelicerates comprise two marine groups: Sea spiders and horseshoe crabs, and the terrestrial arachnids. These have been thought to be related as shown below.[40][43] (Pycnogonida (sea spiders) may be excluded from the chelicerates, which are then identified as the group labelled "Euchelicerata".[45]) A 2019 analysis nests Xiphosura deeply within Arachnida.[46]
Discovering relationships within the arachnids has proven difficult as of March 2016[update], with successive studies producing different results. A study in 2014, based on the largest set of molecular data to date, concluded that there were systematic conflicts in the phylogenetic information, particularly affecting the orders
Acariformes,
Parasitiformes and
Pseudoscorpiones, which have had much faster evolutionary rates. Analyses of the data using sets of genes with different evolutionary rates produced mutually incompatible
phylogenetic trees. The authors favoured relationships shown by more slowly evolving genes, which demonstrated the monophyly of Chelicerata, Euchelicerata and Arachnida, as well as of some clades within the arachnids. The diagram below summarizes their conclusions, based largely on the 200 most slowly evolving genes; dashed lines represent uncertain placements.[43]
Tetrapulmonata, here consisting of
Araneae,
Amblypygi and
Uropygi (Thelyphonida s.s.) (
Schizomida was not included in the study), received strong support. Somewhat unexpectedly, there was support for a clade comprising
Opiliones,
Ricinulei and
Solifugae, a combination not found in most other studies.[43] In early 2019, a molecular phylogenetic analysis placed the horseshoe crabs,
Xiphosura, as the sister group to Ricinulei. It also grouped pseudoscorpions with mites and ticks, which the authors considered may be due to
long branch attraction.[46] The addition of
Scorpiones to produce a clade called Arachnopulmonata was also well supported. Pseudoscorpiones may also belong here, as all six orders share the same ancient whole
genome duplication,[47] and analyses support pseudoscorpions as the sister group of scorpions.[48] Genetic analysis has not yet been done for Ricinulei, Palpigradi, or Solifugae, but horseshoe crabs have gone through two whole genome duplications, which gives them five Hox clusters with 34
Hox genes, the highest number found in any invertebrate, yet it is not clear if the oldest genome duplication is related to the one in Arachnopulmonata.[49][50]
More recent phylogenomic analyses that have densely sampled both genomic datasets and morphology have supported horseshoe crabs as nested inside Arachnida, suggesting a complex history of terrestrialization.[51][52] Morphological analyses including fossils tend to recover the Tetrapulmonata, including the extinct group the
Haptopoda,[53][54][55][56][57] but recover other ordinal relationships with low support.
A fossil arachnid in 100 million year old (mya)
amber from Myanmar, Chimerarachne yingi, has spinnerets (to produce silk); it also has a tail, like the
Palaeozoic Uraraneida, some 200 million years after other known fossils with tails. The fossil resembles the most primitive living spiders, the
mesotheles.[59][53]
Taxonomy
The subdivisions of the arachnids are usually treated as
orders. Historically,
mites and
ticks were treated as a single order, Acari. However, molecular phylogenetic studies suggest that the two groups do not form a single clade, with morphological similarities being due to convergence. They are now usually treated as two separate taxa – Acariformes, mites, and Parasitiformes, ticks – which may be ranked as orders or superorders. The arachnid subdivisions are listed below alphabetically; numbers of species are approximate.
Solifugae – solpugids, windscorpions, sun spiders or camel spiders (1,200 species)
Uropygi (also called Thelyphonida) – whip scorpions or vinegaroons, forelegs modified into sensory appendages and a long tail on abdomen tip (120 species)
Extinct forms
†
Haptopoda – extinct arachnids apparently part of the
Tetrapulmonata, the group including spiders and whip scorpions (1 species)
†
Phalangiotarbida – extinct arachnids of uncertain affinity (30 species)
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