The Golden Silk Orb-Weavers (genus Nephila)
The golden silk orb-weavers (genus Nephila) are a genus of spiders noted for the impressive webs they weave. Nephila consists of numerous individual species found around the world. They are also commonly called golden orb-weavers, giant wood spiders or banana spiders. In North America, the golden silk orb-weavers (see also Nephila clavipes) are sometimes referred to as writing spiders due to occasional zigzag patterns (stabilimenta) built into their webs, though these occur much more frequently in the webs of Argiope, such as the St Andrew's Cross spider.
The name of the golden silk orb-weavers refers to the color of the spider silk, not the color of the spider itself.
Yellow threads of their web shine like gold in sunlight. Xanthurenic acid, two quinones and an unknown fourth compound contribute to the yellow color. Experimental evidence suggests that the silk's color may serve a dual purpose: sunlit webs ensnare bees that are attracted to the bright yellow strands, whereas in shady spots the yellow blends in with background foliage to act as a camouflage. The spider is able to adjust pigment intensity relative to background light levels and color; the range of spectral reflectance is specifically adapted to insect vision.
The webs of most Nephila spiders are complex, with a fine-meshed orb suspended in a maze of non-sticky barrier webs. As with many weavers of sticky spirals, the orb is renewed regularly if not daily, apparently because the stickiness of the orb declines with age. When weather is good (and no rain has damaged the orb web), subadult and adult Nephila often rebuild only a portion of the web. The spider will remove and consume the portion to be replaced, build new radial elements, then spin the new spirals. This partial orb renewal is distinct from other orb-weaving spiders that usually replace the entire orb web.
Typically, the golden orb-weaver first weaves a non-sticky spiral with space for 2-20 more spirals in between (the density of sticky spiral strands decreases with increasing spider size). When she has completed the coarse weaving, she returns and fills in the gaps. Whereas most orb-weaving spiders remove the non-sticky spiral when spinning the sticky spiral, Nephila leave it. This produces a "staff paper" effect when the orb is seen in the sun: groups of sticky spirals reflecting light with "gaps" where the non-sticky spiral does not reflect the light.
The circular-orb portion of a mature N. clavipes web can be more than 1 meter across, with support strands extending perhaps many more feet away. In relation to the ground, the webs of adults may be woven anywhere from eye-level upwards high into the tree canopy. The orb web is usually truncated by a top horizontal support strand, giving it an incomplete look.
Adjacent to one face of the main orb there may be a rather extensive and haphazard-looking network of guard-strands suspended a few inches distant across a free-space. This network is often decorated with a lumpy string or two of plant detritus and insect carcasses clumped with silk. This "barrier web" may function as a kind of early-warning system for incoming prey or against spider-hunting predators, or as a shield against windblown leaves; it may also be remnants of the owner's previous web. At least one reference explains the suspended debris-chain as a cue for birds to avoid blundering into and destroying the web.
Stabilimenta among N. clavipes are sometimes seen in the webs of immatures nearing molt, hence the names "molting webs" or "skeleton webs" (webs with radial strands but no spiral elements).
Young spiders do not generally build yellow-colored silk, and the young Nephila themselves can be easily mistaken for young Orchard Spiders (Leucauge) in general color and shape (both species sport silver stripes or patches on their abdomens, described in some references as a form of heat control). The best distinction between Leucauge and Nephila juveniles is web structure: Leucauge tends to build a horizontal orb that is a perfect circle, whereas Nephila build vertical, elliptical orbs that are incomplete (missing the portion of the orb over the hub, the center where the spider sits). Nephila seem to prefer more open habitat such as second-growth scrub or forest edges. Fences or building overhangs often do just as nicely.
In addition, young spiders demonstrate vibrational motion when approached by a predator. They will oscillate at approximately 40 Hz when the web is plucked — thought to be a response to a potential predator. If a predator persists in an attack, the spider will either run to a web-support strand and thus to nearby vegetation, bail out of the web on a silk line that remains connected to the web, or jump from the web after inducing oscillations in the web that aid the jump.
The Australian golden silk orb-weaver (Nephila edulis) has been observed on windy, rainy days dismantling the lower part of its web to allow strong wind to flow through a large opening in the web without breaking it.
Golden Orb Weavers have been seen and photographed eating small birds captured in their webs in Queensland, Australia.
N. clavipes (and many other Nephila species) are frequently victimized by Argyrodes, a genus of very small black-and-silver spiders that are kleptoparasitic. As many as a few dozen may infest a single Nephila web to feed from the host spider's captured prey. The frequent rebuilding or abandoning of webs by Nephila may be a tactic for controlling Argyrodes.
Golden silk orb-weavers are widespread in warmer regions throughout the world, with species in Australia, Asia, Africa (including Madagascar), and the Americas. One species, N. clavipes, occurs in the United States of America, where it ranges throughout the coastal southeast and inland, from North Carolina to Texas.
Nephila and humans
The venom of the golden silk orb-weaver is potent, but not lethal to humans. Its venom is a neurotoxin similar to that of the black widow spider; however, its venom is not nearly as powerful. Its bite causes local pain, redness, and blisters, but these symptoms usually disappear within a day (though the bite mark may leave a scar).
There were efforts to produce garments from Nephila silk. The spiders were fastened and the extruding thread coiled up until the spider was exhausted. However, this method did not prove commercially viable. Fishermen on coasts of the indopacific ocean remove Nephila webs and form them into a ball, which is thrown into the water. There it unfolds and is used to catch bait fish.
Nine golden orb-weavers from Australia perished in the Space Shuttle Columbia disaster. The "AstroSpider" experiment is part of an international program (STARS) that encourages students to design experiments for flight on the US Space Shuttle or International Space Station.
Spiders are air-breathing chelicerate arthropods that have two body segments, eight legs, and no chewing mouth parts. About 40,000 species have been identified. In spiders' bodies the usual arthropod segments are fused into two tagmata, the cephalothorax and abdomen, joined by a small, cylindrical pedicel. As in all arthropods the coelom is very small and the main body cavity is a hemocoel through which hemolymph delivers oxygen and nutrients to the tissues and removes waste products. The gut is so narrow that spiders cannot eat large lumps of solid matter, and spiders liquidize their food by flooding it with digestive enzymes and grinding it with the appendages around their mouths. In all except the most primitive group, the Mesothelae, spiders have the most centralized nervous systems of all arthropods, as all their ganglia are fused into one mass in the cephalothorax. Unlike most arthropods, spiders have no extensor muscles in their limbs and instead extend them by hydraulic pressure. Their abdomens bear appendages that have been modified into spinnerets that extrude silk from up to six types of silk gland within their abdomens. Spider silk provides a combination of lightness, strength and elasticity that is superior to that of synthetic materials, and spider silk genes have been inserted into mammals and plants to see if these can be used as silk factories. As a result of their wide range of behaviors, spiders have become common symbols in art and mythology, symbolizing various combinations of patience, cruelty and creative powers.
A vegetarian species was described in 2007, but all others are predators, mostly preying on insects and on other spiders, although a few large species also take birds and lizards. However the young of many spiders supplement their diet with nectar and there is statistical evidence that adults supplement theirs with pollen. Spiders' chelicerae are modified into fangs, which in most cases can inject venom into prey. While the venom of a few species is dangerous to humans, scientists are now researching the use of spider venoms in medicine and as non-polluting pesticides. Spiders capture prey by trapping it in sticky webs, waiting in ambush for it or running it down. Species that use webs or ambush tactics are extremely sensitive to vibrations in the air, ground and silk threads that they use as tripwires, while the active hunters have eyesight up to ten times as acute as that of dragonflies. Some active hunters also use different tactics for different prey, and show signs of intelligence by trying a variety of tactics against difficult prey and by learning very quickly what tactics to adopt against unfamiliar prey. Others have modified bodies and behavior patterns that enable them to mimic ants on which they prey. Spider's webs vary widely in size, shape and the amount of sticky thread used. It now appears that the spiral orb web may be one of the earliest forms. Orb-web spiders, although well-known and the most extensively studied, are a minority of spider species and spiders that produce other types of web are more abundant, possibly because their tangled webs present greater obstacles to predatory wasps.
In males spiders the pedipalps (appendages just below / behind the mouth) are modified as syringes that inject sperm into females' genitalia. To avoid being eaten before they can mate, male spiders identify themselves by a variety of complex courtship rituals. Males of most species survive a few matings, limited mainly by their short life spans, and in a few species males live for a while in their mates' webs. However males of a few species impale themselves on the females' fangs while mating, perhaps because ensuring that their mates are well-fed increases the likely number of offspring. Female spiders weave silk egg-cases, each of which may contain hundreds of eggs; the spiders then hatch as apparently miniature adults, although most are incapable of feeding until after their first molt. Females of many species care for their young, for example by carrying them around or by sharing food with them. A minority of species are social, building communal webs that may house anywhere from a few to 50,000 individuals. Social behavior ranges from precarious toleration, as in the aggressive widow spiders, to co-operative hunting and food-sharing. Although most spiders live for at most two years, tarantulas and other mygalomorph spiders can live up to 25 years in captivity.
Spider-like arachnids with silk-producing spigots appear in the Devonian period about 386 million years ago, but these animals apparently lacked spinnerets. True spiders have been found in Carboniferous rocks from 318 to 299 million years ago, and are very similar to the most primitive surviving order, the Mesothelae. The main groups of modern spiders, Mygalomorphae and Araneomorphae, first appear in the Triassic period, before 200 million years ago. After 130 million years ago fossil amber preserves details of spiders' anatomy and behavior, including mating, killing prey, producing silk and possibly caring for their young. In a few cases amber has preserved spiders' egg sacs and webs, occasionally with prey attached.
Spiders are chelicerates and therefore arthropods. As arthropods 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. Being chelicerates, their bodies consist of two tagmata, sets of segments that serve similar functions: the foremost one, called the cephalothorax or prosoma, is a complete fusion of the segments that in an insect would form two separate tagmata, the head and thorax; the rear tagma is called the abdomen or opisthosoma. The pattern of segment fusion that forms chelicerates' heads is unique among arthropods, and what would normally be the first head segment disappears at an early stage of development, so that chelicerates lack the antennae typical of most arthropods. In fact chelicerates' only appendages ahead of the mouth are a pair of chelicerae, and they lack anything that would function directly as "jaws". The first appendages behind the mouth are called pedipalps, and serve different functions within different groups of chelicerates.
Spiders and scorpions are members of one chelicerate group, the arachnids. While scorpions' chelicerae are generally a modest pair of claws that they use in feeding, spiders' terminate in fangs that are are generally venomous, and fold away behind the upper sections while not in use, while the upper sections generally have thick "beards" that filter solid lumps out of their food, as spiders can take only liquid food; On the other hand scorpions' pedipalps generally form large claws for capturing prey, while those of spiders are fairly small sensors whose bases also act as an extension of the mouth; in addition those of male spiders have enlarged last sections used for sperm transfer.
In spiders the cephalothorax and abdomen are joined by a small, cylindrical pedicel, which enables the abdomen to move independently when producing silk. The upper surface of the cephalothorax is covered by a single, convex carapace while the underside is covered by two rather flat plates. The abdomen is soft and egg-shaped. It shows no sign of segmentation, except that the primitive Mesothelae, whose living members are the Liphistiidae, have segmented plates on the upper surface.
Circulation and respiration; Spider's main organs; Nervous system; Digestive & excretory system; Circulatory system; Respiratory system; Reproductive system: 1 Fang (chelicera); 2 Venom gland; 3 Brain; 4 Pumping stomach; 5 Forward aorta branch; 6 Digestive cecum; 7 Heart; 8 Midgut; 9 Malphigian tubules; 10 Cloacal chamber; 11 Rear aorta; 12 Spinneret; 13 Silk gland; 14 Trachea; 15 Ovary (female); 16 Book lung; 17 Nerve cord; 18 Legs; 19 Pedipalp
Spider's main organs
Like other arthropods, spiders are coelomates in which the coelom is reduced to small areas round the reproductive and excretory systems. Its place is largely taken by a hemocoel, a cavity that runs most of the length of the body and through which blood flows. The heart is a tube in the upper part of the body, with a few ostia that act as non-return valves allowing blood to enter the heart from the hemocoel but prevent it from leaving before it reaches the front end, However in spiders it occupies only the upper part of the abdomen, and blood is discharged into the hemocoel by one artery that opens at the rear end of the abdomen and by branching arteries that pass through the pedicle and open into several parts of the cephalothorax. Hence spiders have open circulatory systems. The blood of many spiders that have book lungs contains the respiratory pigment hemocyanin to make oxygen transport more efficient.
Spiders have developed several different respiratory anatomies, based on book lungs, a tracheal system, or both. Mygalomorph and Mesothelae spiders have two pairs of book lungs filled with haemolymph, where openings on the ventral surface of the abdomen allow air to enter and diffuse oxygen. 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. The trachea system has most likely evolved in small ancestors to help resist desiccation. The trachea were originally connected to the surroundings through a pair of openings called spiracles, but in the majority of spiders this pair of spiracles has fused into a single one in the middle, and moved backwards close to the spinnerets. Spiders that have tracheae generally have higher metabolic rates and better water conservation.
Feeding, digestion and excretion
Uniquely among chelicerates, the final sections of spiders' chelicerae are fangs, and the great majority of spiders can use them to inject venom into prey from venom glands in the roots of the chelicerae. Like most arachnids including scorpions, spiders have a narrow gut that can only cope with liquid food and spiders have two sets of filters to keep solids out. They use one of two different systems of external digestion. Some pump digestive enzymes from the midgut into the prey and then suck the liquified tissues of the prey into the gut, eventually leaving behind the empty husk of the prey. Others grind the prey to pulp using the chelicerae and the bases of the pedipalps, while flooding it with enzymes; in these species the chelicerae and the bases of the pedipalps form a preoral cavity that holds the food they are processing.
The stomach in the cephalothorax acts as a pump that sends the food deeper into the digestive system. The mid gut bears many digestive ceca, compartments with no other exit, that extract nutrients from the food; most are in the abdomen, which is dominated by the digestive system, but a few are found in the cephalothorax.
Most spiders convert nitrogenous waste products into uric acid, which can be excreted as a dry material. Malphigian tubules ("little tubes") extract these wastes from the blood in the hemocoel and dump them into the cloacal chamber, from which they are expelled through the anus. Production of uric acid and its removal via Malphigian tubules are a water-conserving feature that has evolved independently in several arthropod lineages that can live far away from water, for example the tubules of insects and arachnids develop from completely different parts of the embryo. However a few primitive spiders, the sub-order Mesothelae and infra-order Mygalomorphae, retain the ancestral arthropod nephridia ("little kidneys"), which use large amounts of water to excrete nitrogenous waste products as ammonia.
Central nervous system
The basic arthropod central nervous system consists of: a pair of nerve cords running below the gut, with paired ganglia as local control centers in all segments; a brain formed by fusion of the ganglia for the head segments ahead of and behind the mouth, so that the esophagus is encircled by this conglomeration of ganglia. Except for the primitive Mesothelae, of which the Liphistiidae are the sole surviving family, spiders have the much more centralized nervous system that is typical of archnids: all the ganglia of all segments behind the esophagus are fused, so that the cephalothorax is largely filled with nervous tissue and there are no ganglia in the abdomen; in the Mesothelae, the ganglia of the abdomen and the rear part of the cephalothorax remain unfused.
Most spiders have four pairs of eyes on the top-front area of the cephalothorax, arranged in patterns that vary from one family to another. The pair at the front are of the type called pigment-cup ocelli ("little eyes"), which in most arthropods are only capable of detecting the direction from which light is coming, using the shadow cast by the walls of the cup. However the main eyes at the front of spiders' heads are pigment-cup ocelli that are capable of forming images. The other eyes are thought to be derived from the compound eyes of the ancestral chelicerates, but no longer have the separate facets typical of compound eyes. Unlike the main eyes, in many spiders these secondary eyes detect light reflected from a reflective tapetum, and wolf spiders can be spotted by torch light reflected from the tapeta. On the other hand jumping spiders' secondary eyes have no tapeta. Jumping spiders' visual acuity exceeds by a factor of ten that of dragonflies, which have by far the best vision among insects; in fact the human eye is only about five times sharper than a jumping spider's. They achieve this by a telephoto-like series of lenses, a four-layer retina and the ability to swivel their eyes and integrate images from different stages in the scan. The downside is that the scanning and integrating processes are relatively slow.
As with other arthropods, spider's cuticles would block out information about the outside world, except that they are penetrated by many sensors or connections from sensors to the nervous system. In fact spiders and other arthropods have modified their cuticles into elaborate arrays of sensors. Various touch sensors, mostly bristles called setae, respond to different levels of force, from strong contact to very weak air currents. Chemical sensors provide equivalents of taste and smell, often by means of setae. Spider also have in the joints of their limbs slit sensors that detect vibration. In web-building spiders all these mechanical and chemical sensors are more important than the eyes, while the eyes are most important to spiders that hunt actively.
Like most arthropods, spiders lack balance and acceleration sensors and rely on their eyes to tell them which way is up. Arthropods' proprioceptors, sensors that report the force exerted by muscles and the degree of bending in the body and joints, are well understood. On the other hand little is known about what other internal sensors spiders or other arthropods may have.
Although all arthropods use muscles attached to the inside of the exoskeleton to flex their limbs, spiders and a few other groups still use hydraulic pressure to extend them, a system inherited from their pre-arthropod ancestors. As a result a spider with a punctured cephalothorax cannot extend its legs, and the legs of dead spiders curl up. Spiders can generate pressures up to eight times their resting level in order to extend their legs, and jumping spiders can jump up to 50 times their own length by suddenly increasing the blood pressure in the third or fourth pair of legs.
Most spiders that hunt actively, rather than relying on webs, have dense tufts of fine hairs between the paired claws at the tips of their legs. These tufts, known as scopulae, consist of bristles whose ends are split into as many as 1,000 branches, and enable spiders with scopulae to walk up vertical glass and upside down on ceilings. It appears that scopulae get their grip from contact with extremely thin layers of water on surfaces. Spiders, like most other arachnids, keep at least four legs on the surface while walking or running.
Silk is mainly composed of a protein very similar to that used in insect silk. It is initially a liquid, and hardens not by exposure to air but as a result of being drawn out, which changes the internal structure of the protein. It is similar in tensile strength to nylon and biological materials such as chitin, collagen and cellulose, but is much more elastic, in other words it can stretch much further before breaking or losing shape.
Some spiders have a cribellum, a modified spinneret with up to 40,000 spigots, each of which produces a single very fine fiber. The fibers are pulled out by the calamistrum, a comb-like set of bristles on the jointed tip of the cribellum, and combined into a composite woolly thread that is very effective in snagging the bristles of insects. The earliest spiders had cribella, which produced the first silk capable of capturing insects, before spiders developed silk coated with sticky droplets. However most modern groups of spiders have lost the cribellum.
Even species that do not build webs to catch prey use silk in several ways: as wrappers for sperm and for fertilized eggs; as a "safety rope"; for nest-building; and as "parachutes" by the young of some species.
Reproduction and life cycle
Spiders reproduce sexually and fertilization is internal but indirect, in other words the sperm is not inserted into the female's body by the male's genitals but by an intermediate stage. Unlike many land-living arthropods, male spiders do not produce ready-made spermatophores (packages of sperm) but spin small sperm webs on to which they ejaculate and then transfer the sperm to syringe-like structures on the tips of their pedipalps. When a male detects signs of a female nearby he checks whether she is of the same species and whether she is ready to mate; for example in species that produce webs or "safety ropes", the male can identify the species and sex of these objects by "smell".
Spiders generally use elaborate courtship rituals to prevent the large females from eating the small males before fertilization, except where the male is so much smaller that he is not worth eating. In web-weaving species precise patterns of vibrations in the web are a major part of the rituals, while patterns of touches on the female's body are important in many spiders that hunt actively, and may "hypnotize" the female. Gestures and dances by the male are important for jumping spiders, which have excellent eyesight. If courtship is successful, the male injects his sperm from the pedipalps into the female's genital opening, known as the epigyne, on the underside of her abdomen. Female's reproductive tracts vary from simple tubes to systems that include seminal receptacles in which females store sperm and release it when they are ready.
Males of the genus Tidarren amputate one of their palps before maturation and enter adult life with one palp only. The palps are 20% of male's body mass in this species, and detaching one of the two improves mobility. In the Yemeni species Tidarren argo, the remaining palp is then torn off by the female. The separated palp remains attached to the female's epigynum for about four hours and apparently continues to function independently. In the meantime the female feeds on the palpless male. In over 60% of cases the female of the Australian redback spider kills and eats the male after it inserts its second palp into the female's genital opening; in fact the males co-operate by trying to impale themselves on the females' fangs. Observation shows that most male redbacks never get an opportunity to mate, and the "lucky" ones increase the likely number of offspring by ensuring that the females are well-fed. However males of most species survive a few matings, limited mainly by their short life spans. Some even live for a while in their mates' webs.
Females lay up to 3,000 eggs in one or more silk egg sacs, which maintain a fairly constant humidity level. In some species the females die afterwards, but females of other species protect the sacs by attaching them to their webs, hiding them in nests, carrying them in the chelicerae or attaching them to the spinnerets and dragging them along.
Baby spiders pass all their larval stages inside the egg and hatch as spiderlings, very small and sexually immature but similar in shape to adults. Some spiders care for their young, for example a wolf spider's brood cling to rough bristles on the mother's back, and females of some species respond to the "begging" behaviour of their young by giving them their prey, provided it is no longer struggling, or even regurgitate food.
Like other arthropods, spiders have to molt in order to grow as their cuticles ("skins") cannot stretch. In some species males mate with newly-molted females, which are too weak to be dangerous to the males. Most spiders live for only one to two years, although some tarantulas have lived in captivity for up to 25 years.
Spiders occur in a large range of sizes. The smallest, dwarf spiders of the subfamily Erigoninae, are less than 1 mm (about .05 inches) in body length. The largest and heaviest spiders occur among tarantulas, which can have body lengths up to 90 mm (about 3.5 inches) and leg spans up to 250 mm (about 10 inches).
Only three classes of pigment (ommochromes, bilins and guanine) have been identified in spiders, although other pigments have been detected but not yet characterized. Melanins, carotenoids and pterins, very common in other animals, are apparently absent. In some species the exocuticle of the legs and prosoma is modified by a tanning process, resulting in brown coloration. Bilins are found for example in Micrommata virescens, resulting in its green color. Guanine is responsible for the white markings of the European garden spider Araneus diadematus. It is in many species accumulated in specialized cells called guanocytes. In genera such as Tetragnatha, Leucauge, Argyrodes or Theridiosoma, guanine creates their silvery appearance. While guanine is originally an end-product of protein metabolism, its excretion can be blocked in spiders, leading to an increase in its storage. Structural colors occur in some species, which are the result of the diffraction, scattering or interference of light, for example by modified setae or scales. The white prosoma of Argiope results from hairs reflecting the light, Lycosa and Josa both have areas of modified cuticle that act as light reflectors.
Ecology and behavior
Although spiders are generally regarded as predatory, the jumping spider Bagheera kiplingi gets over 90% of its food from fairly solid plant material produced by acacias as part of a mutually beneficial relationship with a species of ant.
Juveniles of some spiders in the families Anyphaenidae, Corinnidae, Clubionidae, Thomisidae and Salticidae feed on plant nectar. Laboratory studies show that they do so deliberately and over extended periods, and periodically clean themselves while feeding. These spiders also prefer sugar solutions to plain water, which indicates that they are seeking nutrients. Since many spiders are nocturnal, the extent of nectar consumption by spiders may have been under-estimated. Nectar contains amino acids, lipids, vitamins and minerals in addition to sugars, and studies have shown that other spider species live longer when nectar is available. Feeding on nectar avoids the risks of struggles with prey, and the costs of producing venom and digestive enzymes.
Various species are known to feed on dead arthropods (scavenging), web silk, and their own shed exoskeletons. Pollen caught in webs may also be eaten, and studies have shown that young spiders have a better chance of survival if they have the opportunity to eat pollen. In captivity, several spider species are also known to feed on bananas, marmalade, milk, egg yolk and sausages. In one praying mantis species, juveniles also actively feed on pollen and adults that capture pollen-laden insects eat the pollen as well.
Methods of capturing prey
The best-known method of prey capture is by means of sticky webs. Varying placement of webs allows different species of spider to trap different insects in the same area, for example flat horizontal webs trap insects that fly up from vegetation underneath while flat vertical webs trap insects in horizontal flight. Web-building spiders have poor vision, but are extremely sensitive to vibrations.
Females of the water spider Argyroneta aquatica build underwater "diving bell" webs which they fill with air and use for digesting prey, molting, mating and raising offspring. They live almost entirely within the bells, darting out to catch prey animals that touch the bell or the threads that anchor it. A few spiders use the surfaces of lakes and ponds as "webs", detecting trapped insects by the vibrations that these cause while struggling.
Net-casting spiders weave only small webs but then manipulate them to trap prey. Those of the genus Hyptiotes and the family Theridiosomatidae stretch their webs and then release them when prey strike them, but do not actively move their webs. Those of the family Deinopidae weave even smaller webs, hold them outstretched between their first two pairs of legs, and lunge and push the webs as much as twice their own body length to trap prey, and this move may increase the webs' area by a factor of up to ten. Experiments have shown that Deinopis spinosus has two different techniques for trapping prey: backwards strikes to catch flying insects, whose vibrations it detects; and forward strikes to catch ground-walking prey that it sees. These two techniques have also been observed in other deinopids. Walking insects form most of the prey of most deinopids, but one population of Deinopis subrufus appears to live mainly on tipulid flies that they catch with the backwards strike.
Mature female bolas spiders of the genus Mastophora build "webs" that consist of only a single "trapeze line", which they patrol. They also construct a bolas made of a single thread, tipped with a large ball of very wet sticky silk. They emit chemicals that resemble the pheromones of moths, and then swing the bolas at the moths. Although they miss on about 50% of strikes, they catch about the same weight of insects per night as web-weaving spiders of similar size. The spiders eat the bolas if they have not made a kill in about 30 minutes, rest for a while, and then make new bolas. Juveniles and adult males are much smaller and do not make bolas. Instead they release different pheromones that attract moth flies, and catch them with their front pairs of legs.
The primitive Liphistiidae, the "trapdoor spiders" (family Ctenizidae) and many tarantulas are ambush predators that lurk in burrows, often closed by trapdoors and often surrounded by networks of silk threads that alert these spiders to the presence of prey. Other ambush predators do without such aids, including many crab spiders, and a few species that prey on bees, which see ultraviolet, can adjust their ultraviolet reflectance to match the flowers in which they are lurking. Wolf spiders, jumping spiders, fishing spiders and some crab spiders capture prey by chasing it, and rely mainly on vision to locate prey.
Some jumping spiders of the genus Portia hunt other spiders in ways that seem intelligent, outflanking their victims or luring them from their webs. Laboratory studies show that Portia's instinctive tactics are only starting points for a trial-and-error approach from which these spiders learn very quickly how to overcome new prey species. However they seem to be relatively slow "thinkers", which is not surprising as their brains are vastly smaller than those of mammalian predators.
Ant-mimicking spiders face several challenges: they generally develop slimmer abdomens and false "waists" in the cephalothorax to mimic the three distinct regions (tagmata) of an ant's body; they wave the first pair of legs in form to their heads to mimic antennae, which spiders lack, and to conceal the fact that they have eight legs rather than six; they develop large color patches round one pair of eyes to disguise the fact that they generally have eight simple eyes, while ants have two compound eyes; they cover their bodies with reflective hairs to resemble the shiny bodies of ants. In some spider species males and females mimic different ant species, as female spiders are usually much larger than males. Ant-mimicking spiders also modify their behavior to resemble that of the target species of ant, for example many adopt a zig-zag pattern of movement, ant-mimicking jumping spiders avoid jumping, and spiders of the genus Synemosyna walk on the outer edges of leaves in the same way as Pseudomyrmex. Ant-mimicry in many spiders and other arthropods may be for protection from predators that hunt by sight, including birds, lizards and spiders. However several ant-mimicking spiders prey either on ants or on the ants "livestock" such as aphids. When at rest the ant-mimicking crab spider Amyciaea does not closely resemble Oecophylla, but while hunting it imitates the behavior of a dying ant to attract worker ants. After a kill some ant-mimicking spiders hold their victims between themselves and large groups of ants to avoid being attacked.
There is strong evidence that spiders' coloration is camouflage that helps them to evade their major predators, birds and parasitic wasps, both of which have good color vision. Many spider species are colored so as to merge with their most common backgrounds, and some have disruptive coloration, stripes and blotches that break up their outlines. In a few species, such as the Hawaiian happy-face spider, Theridion grallator, several coloration schemes are present in a ratio that appears to remain constant, and this may make it more difficult for predators to recognize the species. Most spiders are insufficiently dangerous or unpleasant-tasting for warning coloration to offer much benefit. However a few species with powerful venoms, large jaws or irritant hairs have patches of warning colors, and some actively display these colors when threatened.
Many of the family Theraphosidae, which includes tarantulas and baboon spiders, have urticating hairs on their abdomens and use their legs to flick them at attackers. These hairs are fine setae (bristles) with fragile bases and a row of barbs on the tip. The barbs cause intense irritation but there is no evidence that they carry any kind of venom. A few defend themselves against wasps by including networks of very robust threads in their webs, giving the spider time to flee while the wasps are struggling with the obstacles. The golden wheeling spider Carparachne aureoflava of the Namibian desert escapes parasitic wasps by flipping onto its side and cartwheeling down sand dunes.
A few species of spiders that build webs live together in large colonies and show social behavior, although not as complex as in social insects. Anelosimus eximius (in the family Theridiidae) can form colonies of up to 50,000 individuals. The genus Anelosimus has a strong tendency towards sociality: all known American species are social, and species in Madagascar are at least somewhat social. Members of other species in the same family but several different genera have independently developed social behavior. For example although Theridion nigroannulatum belongs to a genus with no other social species, T. nigroannulatum build colonies thay may contain several thousand individuals that co-operate in prey capture and share food. Other communal spiders include several Philoponella species (family Uloboridae), Agelena consociata (family Agelenidae) and Mallos gregalis (family Dictynidae). Social predatory spiders need to defend their prey against kleptoparasites ("thieves"), and larger colonies are more successful in this. The vegetarian spider Bagheera kiplingi lives in small colonies which help to protect eggs and spiderlings. Even widow spiders (genus Latrodectus), which are notoriously aggressive and cannibalistic, have formed small colonies in captivity, sharing webs and feeding together.
There is no consistent relationship between the classification of spiders and the types of web they build: species in the same genera may build very similar or significantly different webs. Not is there much correspondence between spiders' classification and the chemical composition of their silks. Convergent evolution in web construction, in other words use of similar techniques by remotely-related species, is "rampant". Non-orb web designs and the spinning behaviors that produce them have received very little attention from arachnologists, despite the fact that the majority of spiders build non-orb webs. The basic radial-then-spiral sequence visible in orb webs and the "sense of direction" required to build them may have been inherited from the common ancestors of most spider groups. It used to be thought that the sticky orb web was an evolutionary innovation resulting in the diversification of the Orbiculariae. Now, however, it appears that non-orb spiders are a sub-group that evolved from orb-web spiders, and non-orb spiders have over 40% more species and are four times as abundant as orb-web spiders. Their greater success may be due to the fact that sphecid wasps, which are often the dominant predators on spiders, much prefer to attack spiders that have flat webs.
About half the potential prey that hit orb webs escape. A web has to perform three functions: intercepting the prey (intersection); absorbing its momentum without breaking (stopping); and trapping the prey by entangling it or sticking to it (retention). No single design is best for all prey. For example: wider spacing of lines will increase the web's area and hence its ability to intercept prey, but reduce its stopping power and retention; closer spacing, larger sticky droplets and thicker lines would improve retention, but would make it easier for potential prey to see and avoid the web,at least during the day. However there are no consistent differences between orb webs built for use during the day and those built for use at night. In fact there is no simple relationship between orb web design features and they prey they capture, as each orb-weaving species takes a wide range of prey.
The hubs of orb webs, where the spiders lurk, are usually above the center as the spiders can move downwards faster than upwards. If there is an obvious direction in which the spider can retreat to avoid its own predators, the hub is usually offset towards that direction.
Horizontal orb webs are fairly common, despite being less effective at intercepting and retaining prey and more vulnerable to damage by rain and falling debris. Various researchers have suggested that horizontal webs offer compensating advantages, such as: reduced vulnerability to wind damage; reduced visibility to prey flying upwards, because of the back-lighting from the sky; enabling oscillations to catch insects in slow horizontal flight. However there is no single explanation for the common use of horizontal orb webs.
Spiders often attach highly visible silk bands called decorations or stabilimenta to their webs. Field research suggests that webs with more decorative bands captured more prey per hour. However a laboratory study showed that spiders reduce the building of these decorations if they sense the presence of predators.
There are several unusual variants of orb web, many of them convergently evolved, including: attachment of lines to the surface of water, possibly to trap insects in or on the surface; webs with twigs through their centers, possibly to hide the spiders from predators; "ladder-like" webs that appear most effective in catching moths. However the significance of many variations is unclear.
In 1973, Skylab 3 took two orb-web spiders into space to test their web-spinning capabilities in zero gravity. At first both produced rather sloppy webs, but they adapted quickly.
Other types of webs
The Linyphiidae generally make horizontal but uneven sheets, with tangles of stopping threads above. Insects that hit the stopping threads fall on to the sheet or are shaken on to it by the spider, and are held by sticky threads on the sheet until the spider can attack from below.
Spider fossils are rare because spiders' bodies are very soft. The oldest known amber that contains fossil arthropods dates from 130 million years ago in the Early Cretaceous period. In addition to preserving spiders' anatomy in very fine detail, pieces of amber show spiders mating, killing prey, producing silk and possibly caring for their young. In a few cases amber has preserved spiders' egg sacs and webs, occasionally with prey attached; the oldest fossil web found so far is 100 million years old. Earlier spider fossils come from a few lagerstatten, places where conditions were exceptionally suited to preserving fairly soft tissues.
The oldest known arachnid is the trigonotarbid Palaeotarbus jerami, from about 420 million years ago in the Silurian period, and had a triangular cephalothorax and segmented abdomen, as well as eight legs and a pair of pedipalps. Attercopus fimbriunguis, from 386 million years ago in the Devonian period, bears the earliest known silk-producing spigots, and was therefore hailed as a spider. However these spigots may have been mounted on the underside of the abdomen rather than on spinnerets, which are modified appendages and whose mobility is important in the building of webs. Hence Attercopus and the similar Permian archnid Permarachne may not have been true spiders, and probably used silk for lining nests or producing egg-cases rather than for building webs.
Several Carboniferous spiders were members of the Mesothelae, a primitive group now represented only by the Liphistiidae. The mesothelid Paleothele montceauensis, from the Late Carboniferous over 299 million years ago, had five spinnerets. Although the Permian period 299 to 251 million years ago saw rapid diversification of flying insects, there are very few fossil spiders from this period.
The main groups of modern spiders, Mygalomorphae and Araneomorphae, first appear in the Triassic well before 200 million years ago. Some Triassic mygalomorphs appear to be members of the family Hexathelidae, whose modern members include the notorious Sydney funnel-web spider, and their spinnerets appear adapted for building funnel-shaped webs to to catch jumping insects. Araneomorphae account for the great majority of modern spiders, including those that weave the familiar orb-shaped webs. The Jurassic and Cretaceous periods provide a large number of fossil spiders, including representatives of many modern families.
It is now agreed that spiders (Araneae) are monophyletic, in other words members of a group that contains a common ancestor plus all and only its descendants. There has been debate about what are their closest evolutionary relatives and how all of these evolved from the ancestral chelicerates, which were marine animals. The cladogram on the right is based on J.W. Shultz' analysis (2007). Other views include proposals that: scorpions are more closely related to the extinct marine scorpion-like eurypterids than to spiders; spiders and Amblypygi are a monopyhletic group. The appearance of several multi-way branchings in the tree on the right shows that there are still uncertainties about relationships between the groups involved.
Arachnids lack some features of other checlicerates, including backward-pointing mouths and gnathobases ("jaw bases") at the bases of their legs; both of these features are part of the ancestral arthropod feeding system. Instead they have mouths that point forwards and downwards, and all have some means of breathing air. Spiders (Araneae) are distinguished from other arachnid groups by several characteristics, including spinnerets and, in males, pedipalps that are specially adapted for sperm transfer.
Spiders are divided into three sub-orders, Mesothelae, Mygalomorphae and Araneomorphae; the last two are often grouped under the name Opisthothelae. Almost 40,000 living species of spiders (order Araneae) have been identified and are currently grouped into about 110 families and about 3,500 genera by arachnologists.
The only living members of the primitive Mesothelae are the family Liphistiidae, found only in Southeast Asia, China, and Japan. Most of the Liphistiidae construct silk-lined burrows with thin trapdoors, although some species of the genus Liphistius build camouflaged silk tubes with a second trapdoor as an emergency exit. Members of the genus Liphistius run silk "tripwires" outwards from their tunnels to help them detect approaching prey, while those of genus Heptathela do not and instead rely on their built-in vibration sensors. Spiders of the genus Heptathela have no venom glands.
The extinct families Arthrolycosidae, found in Carboniferous and Permian rocks, and Arthromygalidae, so far found only in Carboniferous rocks, have been classified as members of the Mesothelae.
The Mygalomorphae, which first appeared in the Triassic period, are generally heavily-built and hairy, with large, robust chelicerae and fangs. Well-known examples include tarantulas, trapdoor spiders and the Australasian funnel-web spiders. Most spend the majority of their time in burrows, and some run silk tripwires out from these, but a few build webs to capture prey. However mygalomorphs cannot produce the pirifom silk that the Araneomorphae use as instant adhesive to glue silk to surfaces or to other strands of silk, and this makes web construction more difficult for mygalomorphs. Since mygalomorphs rarely "balloon" by using air currents for transport, their populations often form clumps. In addition to arthropods, mygalomorphs prey on frogs and lizards, and snails.
In addition to accounting for over 90% of spider species, the Araneomorphae have the most diverse lifestyles as they include orb-web spiders, the cursorial wolf spiders, and jumping spiders, as well as the only known vegetarian spider.
Most spiders will only bite humans in self-defense, and few produce worse effects than a mosquito bite or bee-sting. Most of those with medically serious bites, such as recluse spiders and widow spiders, are shy and bite only when they feel threatened, although this can easily arise by accident. Funnel web spiders' defensive tactics are aggressive, although they rarely inject much venom. On the other hand the Brazilian wandering spider requires very little provocation. There were about 100 reliably reported deaths from spider bites in the 20th century, but about 1,500 from jellyfish stings. Many alleged cases of spider bites may represent incorrect diagnoses, which would make it more difficult to check the effectiveness of treatments for genuine bites.
Benefits to humans
Cooked tarantula spiders are considered a delicacy in Cambodia, and by the Piaroa Indians of southern Venezuela - provided the highly irritant hairs, the spiders' main defense system, are removed first.
Spider venoms may be a less polluting alternative to conventional pesticides as they are deadly to insects but the great majority are harmless to vertebrates. Australian funnel web spiders are a promising source as most of the world's insect pests have had no opportunity to develop any immunity to their venom, and funnel web spiders thrive in captivity and are easy to "milk". It may be possible to target specific pests by engineering genes for the production of spider toxins into viruses that infect species such as cotton bollworms.
Possible medical uses for spider venoms are being investigated, for the treatment of cardiac arrhythmia, Alzheimer's disease, strokes, and erectile dysfunction.
Because spider silk is both light and very strong, attempts are being made to produce it in goats' milk and in the leaves of plants, by means of genetic engineering.
Arachnophobia is a specific phobia, an abnormal fear of spiders or anything reminiscent of spiders, such as webs or spider-like shapes. It may be an exaggerated form of an instinctive response that helped early humans to survive, or perhaps a cultural phenomenon that is most common in predominantly European societies.
Spiders have been the focus of fears, stories and mythologies of various cultures for centuries. They have symbolized patience due to their hunting technique of setting webs and waiting for prey, as well as mischief and malice for the painful death their venom causes. Web-spinning also caused the association of the spider with creation myths as they seem to have the ability to produce their own worlds. The Moche people of ancient Peru worshipped nature. They placed emphasis on animals and often depicted spiders in their art.
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