The anatomy of spiders includes many characteristics shared with other arachnids. These characteristics include bodies divided into two tagmata (sections or segments), eight jointed legs, no wings or antennae, the presence of chelicerae and pedipalps, simple eyes, and an exoskeleton, which is periodically shed.
Spiders also have several adaptations that distinguish them from other arachnids. All spiders are capable of producing silk of various types, which many species use to build webs to ensnare prey. Most spiders possess venom, which is injected into prey (or defensively, when the spider feels threatened) through the fangs of the chelicerae. Male spiders have specialized pedipalps that are used to transfer sperm to the female during mating. Many species of spiders exhibit a great deal of sexual dimorphism. [1]
Spiders, unlike insects, have only two main body parts (tagmata) instead of three: a fused head and thorax (called a cephalothorax or prosoma) and an abdomen (also called an opisthosoma). The exception to this rule are the assassin spiders in the family Archaeidae, whose cephalothorax is divided into two parts by an elongated "neck". In the majority of spiders, the abdomen is not externally segmented. The exception is the Liphistiidae, a basal family, which retains this more primitive character; hence they are sometimes called segmented spiders. The abdomen and cephalothorax are connected by a thin waist called the pedicel. Unlike insects, spiders have an endoskeleton in addition to their exoskeleton. [2]
The cephalothorax, also called prosoma, is composed of two primary surfaces: a dorsal carapace and a ventral sternum. Most external appendages on the spider are attached to the cephalothorax, including the eyes, chelicerae and other mouthparts, pedipalps and legs.
Like other arachnids, spiders are unable to chew their food, so they have a mouth part shaped like a short drinking straw that they use to suck up the liquefied insides of their prey. However, they are able to eat their own silk to recycle proteins needed in the production of new spider webs. [3] Some spiders, such as the dewdrop spiders ( Argyrodes ), even eat the silk of other spider species. [4]
Spiders typically have eight walking legs (insects have six). They do not have antennae; the pair of appendages in front of the legs are the pedipalps (or just palps). Spiders' legs are made up of seven segments. Starting from the body end, these are the coxa, trochanter, femur, patella, tibia, metatarsus and tarsus. The tip of the tarsus bears claws, which vary in number and size. Spiders that spin webs typically have three claws, the middle one being small; hunting spiders typically have only two claws. Since they do not have antennae, spiders use specialised and sensitive setae on their legs to pick up scent, sounds, vibrations and air currents. [5] Some spiders, such as the Australian crab spider, do not have claws.
The pedipalps have only six segments: the metatarsus is missing. In adult males, the tarsus of each palp is modified to carry an elaborate and often species-specific structure used for mating (variously called a palpal bulb, palpal organ or copulatory bulb). [6] The basal segments of the pedipalps, the coxae, next to the mouth, are modified to assist with feeding, and are termed maxillae, although they are not homologous with the maxillae of mandibulate arthropods. In mesothele and mygalomorph spiders, the maxillae are only slightly modified; in araneomorph spiders, the anterior edge is often saw-like and is used in cutting up prey. [7]
Spiders usually have eight eyes, each with a single lens rather than multiple units as in the compound eyes of insects. The specific arrangement of the eyes is one of the features used in classifying different species. Most species of the Haplogynae have six eyes, although some have eight (Plectreuridae), four (e.g., Tetrablemma) or even two (most Caponiidae). Sometimes one pair of eyes is better developed than the rest, or even, in some cave species, there are no eyes at all. Several families of hunting spiders, such as jumping spiders and wolf spiders, have fair to excellent vision. The main pair of eyes in jumping spiders even sees in color. [8]
Net-casting spiders of genus Deinopis have their posterior median eyes enlarged into large forward-facing compound lenses. These eyes have a wide field of view and are able to gather available light more efficiently than the eyes of cats and owls. This is despite the fact that they lack a reflective layer (tapetum lucidum); instead, each night, a large area of light-sensitive membrane is manufactured within the eyes, and since arachnid eyes do not have irises, it is rapidly destroyed again at dawn. [9]
However, most spiders that lurk on flowers, webs, and other fixed locations waiting for prey tend to have very poor eyesight; instead they possess an extreme sensitivity to vibrations, which aids in prey capture. Vibration sensitive spiders can sense vibrations from such various mediums as the water surface, the soil or their silk threads. Changes in the air pressure can also be detected in search of prey.
The cephalothorax is joined to the abdomen by a thin flexible pedicel. This allows a spider to move its abdomen in all directions, and thus, for example, to spin silk without moving the cephalothorax. This waist is actually the last segment (somite) of the cephalothorax (the pregenital somite).
The abdomen is also known as the opisthosoma. On the ventral side of the abdomen are two hardened plates covering the book lungs. These are called the epigastric plates. A fold, known as the epigastric furrow, separates the region of the book lungs and epigyne from the more posterior part of the abdomen. In the middle of this furrow is the opening of the oviduct (in females) and at either end are the lung slits. [10] In most spiders the external segmentation is no longer visible, but is still noticeable internally. The first abdominal segment behind the pedicel contains both the openings to a pair of book lungs (absent in a few species) and the gonopore (genital opening). Then follows a segment with a second pair of book lungs (replaced with trachea in most modern spiders). The next two segments carry the spinnerets. In the majority of spiders the spinnerets have migrated to the posterior end of the body. The remaining abdominal segments are more difficult to distinguish. [11]
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The abdomen has no appendages except from one to four (usually three) modified pairs of movable telescoping organs called spinnerets, which produce silk. Originally, the common ancestor of spiders had four pairs of spinnerets, with two pairs on the tenth body segment and two pairs on the eleventh body segment, located in the middle on the ventral side of the abdomen. The suborder Mesothelae is unique in having only two types of silk glands – thought to be the ancestral condition. All other spiders have the spinnerets further towards the posterior end of the body where they form a small cluster, and the anterior central spinnerets on the tenth segment are lost or reduced (suborder Mygalomorphae), or modified into a specialised and flattened plate called the cribellum (suborder Araneomorphae). The cribellum (usually separated into a left and a right half) produces a thread made up of hundreds to thousands of very fine dry silk fibers (about 10 nm thick) around a few thicker core fibers, which then are combed into a woolly structure by using a group of specialized hairs on their fourth pair of legs. Once all araneomorph (modern) spiders had a cribellum, but today it only remains in the cribellate spiders (although it is sometimes missing even here), which are widespread around the world. Often, this plate lacks the ability to produce silk, and is then called the colulus. The colulus is reduced or absent in most species. [12] The cribellate spiders were the first spiders to build specialized prey-catching webs, later evolving into groups that used the spinnerets solely to make webs, instead using silk threads dotted with droplets of a sticky liquid (like pearls on a necklace) to capture small arthropods, and a few large species even small bats and birds. Other spiders do not build webs at all, but have become active hunters, like the highly successful jumping spiders.
Spiders, like most arthropods, have an open circulatory system, i.e., they do not have true blood, or the veins which transport it. Rather, their bodies are filled with haemolymph, which is pumped through arteries by a heart into spaces called sinuses surrounding their internal organs. The haemolymph contains hemocyanin, a respiratory protein similar in function to hemoglobin. Hemocyanin contains two copper atoms, tinting the haemolymph with a faint blue color. [13]
The heart is located in the abdomen a short distance within the middle line of the dorsal body-wall, and above the intestine. Unlike in insects, the heart is not divided into chambers, but consists of a simple tube. The aorta, which supplies haemolymph to the cephalothorax, extends from the anterior end of the heart. Smaller arteries extend from sides and posterior end of the heart. A thin-walled sac, known as the pericardium, completely surrounds the heart. [14]
Spiders have developed several different respiratory anatomies, based either on book lungs or on tracheae. Mesothele and mygalomorph spiders have two pairs of book lungs filled with haemolymph, where openings on the ventral surface of the abdomen allow air to enter and oxygen to diffuse in and carbon dioxide to diffuse out. This is also the case for some basal araneomorph spiders like the family Hypochilidae, but the remaining members of this group have just the anterior pair of book lungs intact while the posterior pair of breathing organs are partly or fully modified into tracheae, through which oxygen is diffused into the haemolymph or directly to the tissue and organs. This system has most likely evolved in small ancestors to help resist desiccation. The trachea were originally connected to the surroundings through a pair of spiracles, but in the majority of spiders this pair of spiracles has fused into a single one in the middle, and migrated posterior close to the spinnerets.
Among smaller araneomorph spiders there are species in which the anterior pair of book lungs have also evolved into tracheae, or are simply reduced or missing. In a very few species the book lungs have developed deep channels, apparently signs of evolution into tracheae. Some very small spiders in moist and sheltered habitats do not have any breathing organs at all, as gas exchange occurs directly through their body surface. In the tracheal system oxygen interchange is much more efficient, enabling cursorial hunting (hunting involving extended pursuit) and other advanced characteristics, such as having a smaller heart and the ability to live in drier habitats.
Digestion is carried out internally and externally. Spiders do not have powerful chelicerae, but secrete digestive fluids into their prey from a series of ducts perforating their chelicerae. The coxal glands are excretory organs that lie in the prosoma, and open to the outside at the coxae of the walking legs. In primitive spiders, such as the Mesothelae and the Mygalomorphae, two pairs of coxal glands open onto the posterior side of the first and third coxae. They release a fluid only during feeding and play an important role in ion and water balance. [15] Digestive fluids dissolve the prey's internal tissues. Then the spider feeds by sucking the partially digested fluids out. Other spiders with more powerfully built chelicerae masticate the entire body of their prey and leave behind only a relatively small amount of indigestible materials. Spiders consume only liquid foods. Many spiders will store prey temporarily. Web weaving spiders that have made a shroud of silk to quiet their envenomed prey's death struggles will generally leave them in these shrouds and then consume them at their leisure.
Almost all spiders reproduce sexually. They are unusual in that they do not transfer sperm directly, for example via a penis. Instead the males transfer it to specialized structures (palpal bulbs) on the pedipalps and then meander about to search for a mate. [16] These palps are then introduced into the female's epigyne. This was first described in 1678 by Martin Lister. In 1843 it was revealed that males build a nuptial web into which they deposit a drop of semen, which is then taken up by the copulatory apparatus (the palpal bulb) in the pedipalp. The structure of the copulatory apparatus varies significantly between males of different species. While the widened palpal tarsus of the southern house spider, Kukulcania hibernalis (Filistatidae), only forms a simple bulb containing the coiled blind duct, members of the genus Argiope have a highly complex structure.
Pedipalps are the secondary pair of forward appendages among chelicerates – a group of arthropods including spiders, scorpions, horseshoe crabs, and sea spiders. The pedipalps are lateral to the chelicerae ("jaws") and anterior to the first pair of walking legs.
The Mesothelae are a suborder of spiders. As of April 2024, two extant families were accepted by the World Spider Catalog, Liphistiidae and Heptathelidae. Alternatively, the Heptathelidae can be treated as a subfamily of a more broadly circumscribed Liphistiidae. There are also a number of extinct families.
Solifugae is an order of animals in the class Arachnida known variously as camel spiders, wind scorpions, sun spiders, or solifuges. The order includes more than 1,000 described species in about 147 genera. Despite the common names, they are neither true scorpions nor true spiders. Most species of Solifugae live in dry climates and feed opportunistically on ground-dwelling arthropods and other small animals. The largest species grow to a length of 12–15 cm (5–6 in), including legs. A number of urban legends exaggerate the size and speed of the Solifugae, and their potential danger to humans, which is negligible.
Cribellum literally means "little sieve", and in biology the term generally applies to anatomical structures in the form of tiny perforated plates.
Opisthothelae is a suborder of spiders within the order Araneae, containing Mygalomorphae and Araneomorphae, but excluding Mesothelae. The Opisthothelae are sometimes presented as an unranked clade and sometimes as a suborder of Araneae. In the latter case, Mygalomorphae and Araneomorphae are treated as infraorders.
Opiliones are an order of arachnids and share many common characteristics with other arachnids. However, several differences separate harvestmen from other arachnid orders such as spiders. The bodies of opiliones are divided into two tagmata : the abdomen (opisthosoma) and the cephalothorax (prosoma). Unlike spiders, the juncture between the abdomen and cephalothorax is often poorly defined. Harvestmen have chelicerae, pedipalps and four pairs of legs. Harvestmen were traditionally thought to have two eyes, except in the case of eyeless species. Developmental genetic work has shown that living species retain up to six eyes, including one pair of rudimentary median eyes and one pair of rudimentary lateral eyes.
Unicorn ("one horn", in Latin) is a genus of goblin spiders from South America, containing seven species that occur predominantly in high elevation, semi-desert regions of Bolivia, Chile, and Argentina. Individuals are relatively large for goblin spiders, measuring up to 3.0 mm (0.12 in) in body length. The genus name refers to a characteristic pointed projection between the eyes and jaws of males. In at least one species, broken-off tips of the male pedipalps have been found within the genitalia of females, postulated as a means of sperm competition. Unicorn possesses several traits that suggest it is a relatively "primitive" member of the Oonopidae, and is classified with other similar, soft-bodied goblin spiders in the subfamily Sulsulinae.
Tarantulas comprise a group of large and often hairy spiders of the family Theraphosidae. As of December 2023, 1,100 species have been identified, with 166 genera. The term "tarantula" is usually used to describe members of the family Theraphosidae, although many other members of the same infraorder (Mygalomorphae) are commonly referred to as "tarantulas" or "false tarantulas". Some of the more common species have become popular in the exotic pet trade. Many New World species kept as pets have setae known as urticating hairs that can cause irritation to the skin, and in extreme cases, cause damage to the eyes.
Spiders are air-breathing arthropods that have eight limbs, chelicerae with fangs generally able to inject venom, and spinnerets that extrude silk. They are the largest order of arachnids and rank seventh in total species diversity among all orders of organisms. Spiders are found worldwide on every continent except Antarctica, and have become established in nearly every land habitat. As of November 2023, 51,673 spider species in 136 families have been recorded by taxonomists. However, there has been debate among scientists about how families should be classified, with over 20 different classifications proposed since 1900.
Psalmopoeus irminia, also known as the Venezuelan suntiger, is a species of tarantula endemic to Venezuela, Guyana and Brazil. They were first described in 1994 by F. Saager.
This glossary describes the terms used in formal descriptions of spiders; where applicable these terms are used in describing other arachnids.
Agelena labyrinthica is a species of spider in the family Agelenidae. It is a widespread species in Europe and its range extends to Central and East Asia.
Aptostichus barackobamai is a large species of trapdoor spider in the family Euctenizidae named after the 44th President of the United States, Barack Obama. The species was first reported by Jason Bond of Auburn University in December 2012 as one of 33 new species of the genus Aptostichus. The species is endemic throughout northern California, forming burrows out of silk, dirt, and sand, from which it attacks prey. This spider is identified by its dark red to red-brown coloration with a stripped or chevron patterned abdomen. Breeding occurs during the winter and females tend to be larger than their male counterparts. A. barackobamai is part of the larger Aptostichus icenoglei species complex, and is a close relative to Aptostichus icenoglei and Aptostichus isabella.
Progradungula otwayensis, commonly known as the odd-clawed spider, is a species of cribellate spider endemic to the Great Otway National Park of Victoria, Australia. It is one of only two species in the gradungulid genus Progradungula.
The two palpal bulbs – also known as palpal organs and genital bulbs – are the copulatory organs of a male spider. They are borne on the last segment of the pedipalps, giving the spider an appearance often described as like wearing boxing gloves. The palpal bulb does not actually produce sperm, being used only to transfer it to the female. Palpal bulbs are only fully developed in adult male spiders and are not completely visible until after the final moult. In the majority of species of spider, the bulbs have complex shapes and are important in identification.
Hypochilus thorelli is a species of spider in the family Hypochilidae. Unlike almost all other araneomorph or "true" spiders, members of the family have four book lungs. They are often called "lampshade spiders" because of the shape of their webs which are usually built underneath ledges or projections. H. thorelli is found in the southern Appalachian Mountains of the eastern United States.
Thiratoscirtus obudu is a species of jumping spider in the genus Thiratoscirtus that lives in Nigeria. The species was first described in 2011 by Wanda Wesołowska and Russell-Smith. The holotype was found at an altitude of 1,900 m (6,200 ft) above sea level. on Obudu Plateau, Cross River State, after which it is named. Only the male has been described. It is a medium-sized spider, with a wider cephalothorax that is between 2.7 and 2.8 mm long and a thinner abdomen that is 2.2 and 2.4 mm in length, both oval in shape. The mouthparts include robust chelicerae and a short fang. It can be distinguished from other spiders in the genus by its copulatory organs. It has a small pedipalp with a rounded palpal bulb and a small spike on its palpal tibia called a tibial apophysis The apophysis is smaller than that found on other species.
Euophrys nana is a species of jumping spider in the genus Euophrys that is endemic to South Africa. The species was first described in 2014 by Wanda Wesołowska, Galina Azarkina and Anthony Russell-Smith. It is a small spider, with a body that consists of a cephalothorax that is typically 1 mm (0.04 in) long and an abdomen that is typically 1.5 mm (0.06 in) long. The carapace, the topside of the cephalothorax is brown a central yellow stripe. The underside of the cephalothorax, or sternum, is yellowish-brown. The abdomen has a distinctive pattern of brown and white stripes around its entire body. It is this pattern that differentiates the spider from related species. The copulatory organs are also unique amongst spiders in the genus, particularly the very long thin embolus on the palpal bulb of the male. The female has not been described.
Chimerarachne is a genus of extinct arachnids, containing five species. Fossils of Chimerarachne were discovered in Burmese amber from Myanmar which dates to the mid-Cretaceous, about 100 million years ago. It is thought to be closely related to spiders, but outside any living spider clade. The earliest spider fossils are from the Carboniferous, requiring at least a 170 myr ghost lineage with no fossil record. The size of the animal is quite small, being only 2.5 millimetres (0.098 in) in body length, with the tail being about 3 millimetres (0.12 in) in length. These fossils resemble spiders in having two of their key defining features: spinnerets for spinning silk, and a modified male organ on the pedipalp for transferring sperm. At the same time they retain a whip-like tail, rather like that of a whip scorpion and uraraneids. Chimerarachne is not ancestral to spiders, being much younger than the oldest spiders which are known from the Carboniferous, but it appears to be a late survivor of an extinct group which was probably very close to the origins of spiders. It suggests that there used to be spider-like animals with tails which lived alongside true spiders for at least 200 million years.
Detalik anthonyi is the type species for the genus Detalik. It is a species of jumping spider that is endemic to Nigeria and was first described in 2021 by Wanda Wesołowska. A small spider like all those in the genus, it has a cephalothorax measuring between 1.7 and 2.2 mm long and an abdomen between 1.5 and 2.7 mm long. The cephalothorax has a brown top or carapace that has wide white stripes on its back and a yellow underside or sternum. The abdomen differs between the sexes. The female abdomen is brownish-grey with a lighter streak running down it while the male has a mosaic-like pattern of brown dots at the very rear. The spider has distinctive copulatory organs. The male has an irregular-shaped palpal bulb with characteristic spikes, or apophyses. One, that is attached to the bulb itself, is large and sickle-shaped; two others are much shorter. The female has copulatory openings to the sides of the epigyne that lead to particularly long insemination ducts.
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