Spider behavior refers to the range of behaviors and activities performed by spiders. Spiders are air-breathing arthropods that have eight legs and chelicerae with fangs that inject venom. They are the largest order of arachnids and rank seventh in total species diversity among all other groups of organisms which is reflected in their large diversity of behavior.
Almost all known spider species are predators, mostly preying on insects and on other spiders, although a few species also take vertebrates such as frogs, lizards, fish, and even birds and bats. Spiders' guts are too narrow to take solids, and they liquidize their food by flooding it with digestive enzymes and grinding it with the bases of their pedipalps, as they do not have true jaws.
Though most known spiders are almost exclusively carnivorous, a few species, primarily of jumping spiders, supplement their diet with plant matter such as sap, nectar, and pollen. However, most of these spiders still need a mostly carnivorous diet to survive, and lab studies have shown that they become unhealthy when fed only plants. One exception is a species of jumping spider called Bagheera kiplingi, which is largely herbivorous, feeding mainly on the sugar rich Beltian bodies produced by acacia plants.
Many spiders, but not all, build webs. Other spiders use a wide variety of methods to capture prey.
Web: There are several recognised types of spider web
- Spiral orb webs, associated primarily with the family Araneidae
- Tangle webs or cobwebs, associated with the family Theridiidae
- Funnel webs,
- Tubular webs, which run up the bases of trees or along the ground
- Sheet webs
The net-casting spider weaves a small net which it attaches to its front legs. It then lurks in wait for potential prey and when such prey arrives, lunges forward to wrap its victim in the net, bite and paralyze it. Hence, this spider expends less energy catching prey than a primitive hunter and also avoids the energy loss of weaving a large orb web.
Bolas: Bolas spiders are unusual orb-weaver spiders that do not spin the webs. Instead, they hunt by using a sticky 'capture blob' of silk on the end of a line, known as a 'bolas'. By swinging the bolas at flying male moths or moth flies nearby, the spider may snag its prey rather like a fisherman snagging a fish on a hook. Because of this, they are also called angling or fishing spider. The prey is lured to the spider by the production of up to three pheromone analogues.
Hunting on land: Jumping spiders, Wolf spiders and many other types of spiders hunt freely. Some of these have enhanced eyesight, sometimes approaching that of a pigeon (although with a much smaller field of vision). They are generally robust and agile. Some are opportunistic hunters pouncing upon prey as they find it or even chasing it over short distances. Some will wait for passing prey in or near the mouth of a burrow.
Hunting on water: Dolomedes spiders hunt by waiting at the edge of a pool or stream. They hold on to the shore with their back legs while the rest of their body lies on the water, with legs stretched out. When they detect the ripples from prey, they run across the surface to subdue it using their foremost legs, which are tipped with small claws; like other spiders they then inject venom with their hollow jaws to kill and digest the prey. They mainly eat insects, but some larger species are able to catch small fish.
Female water spiders (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.
Deception: Some spiders hunt other spiders using deception; the jumping spider Portia mimics the movement of captured insect prey on the webs of other spiders. This attracts the owner of the web whereupon Portia pounces and overwhelms the owner.
Trapdoor: Trapdoor spiders construct burrows with a cork-like trapdoor made of soil, vegetation and silk. The trapdoor is difficult to see when it is closed because the plant and soil materials effectively camouflage it. The trapdoor is hinged on one side with silk. The spiders typically wait for prey while holding on to the underside of the door. Prey is captured when insects, other arthropods, or small vertebrates disturb the 'trip' lines the spider lays out around its trapdoor, alerting the spider to a meal within reach. The spider detects the prey by vibrations and, when it comes close enough, leaps out of its burrow to make the capture. Some Conothele species do not build a burrow, but construct a silken tube with trapdoor in bark crevices.
Basket: The Kaira spider uses a pheromone to attract moths and catches the insects with a basket formed from its legs.
Spiders perform cannibalism under a range of circumstances.
Females eating males: Perhaps the most widely known example of cannibalism in spiders is when females cannibalise males before, during or after copulation. For example, the male Australian redback spider (Latrodectus hasselti) is killed by the female after he inserts his second palpus in the female's genital opening; in over 60% of matings, the female then eats the male. However, the theory of the "sacrificial male" may have become greater than the truth. Some believe that this form of cannibalism only occurs in exceptional cases.
Males eating females: Male water spiders (Argyroneta aquatica) show a predilection for mating with larger females, while cannibalizing females smaller than themselves.
Non-reproductive cannibalism: Some spiders, such as Pholcus phalangioides, will prey on their own kind when food is scarce.
Death feigning can be used in reproductive behavior of spiders. In the nursery web spider, the male sometimes feigns death to avoid getting eaten by females during mating.
Other arachnids may reproduce asexually or sexually. This is seeing as their class makes up 3% of the animal kingdom. Some species are famous for the fact that the female tends to eat the male following copulation. They behave by running around on trees and in bushes and in tightly packed areas so they stay distracted from the others around them.
Spiders exhibit varying levels of sociality. Whereas most spiders are solitary and even aggressive toward other members of their own species, some hundreds of species in several families show a tendency to live in groups, often referred to as colonies. These can form relatively long-lasting aggregations. Some of these aggregations can contain as many as 50,000 individuals as in the case of Anelosimus eximius (in the family Theridiidae). The level of sociality often varies between species (interspecies) but can vary within a species (intraspecies) as well. Many of these social spiders show cooperative brood care, use the same nest (web), and have some amount of generational overlap. A few species, such as Anelosimus eximius, exhibit reproductive division of labor. Some biologists argue that this classifies these species as fully eusocial as these non-reproductives can be considered a non-sterile worker caste. This reproductive division of labor is a result of resource availability and monopolization of those resources.
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. Spiders can generate pressures up to eight times their resting level 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. Unlike smaller jumping spiders, though larger spiders use hydraulics to straighten their legs, they depend on their flexor muscles to generate the propulsive force for their jumps.
Ballooning is a term used for the mechanical kiting spiders use to disperse through the air. A spider or spiderling after hatching will climb as high as it can. The spider then stands on raised legs with its abdomen pointed upwards. After that, it starts releasing several silk threads from its abdomen into the air, which automatically form a triangular shaped parachute. The spider can then let itself be carried away by updrafts of winds, where even the slightest of breeze will suffice.
Spiders have been used in studies which indicate that invertebrates may experience pain. Under natural conditions, orb-weaving spiders (Argiope spp.) undergo autotomy (self-amputation) if they are stung in a leg by wasps or bees. Under experimental conditions, when spiders were injected in the leg with bee or wasp venom, they shed this appendage. But if they are injected with only saline, they rarely autotomize the leg, indicating it is not the physical insult or the ingress of fluid per se that causes autotomy. Spiders injected with venom components which cause injected humans to report pain (serotonin, histamine, phospholipase A2 and melittin) autotomize the leg, but if the injections contain venom components which do not cause pain to humans, autotomy does not occur.
- Sebastin, P.A. and Peter, K.V. (eds). (2009). Spiders of India. Universities Press/Orient Blackswan. ISBN 978-81-7371-641-6
- Watson, Traci (August 11, 2017). "Tiny Spiders Devour Lizards Three Times Their Size". National Geographic.
- Netburn, Deborah (June 19, 2014). "Fish-eating spiders? There are more than anyone thought". Los Angeles Times.
- Nyffeler, Martin; Knörnschild, Mirjam (2013). "Bat Predation by Spiders". PLOS ONE. 8 (3): e58120. doi:10.1371/journal.pone.0058120. PMC 3596325. PMID 23516436.
- Nyffeler, Martin; Olson, Eric G.; Symondson, William Oliver Christian (2016). "Plant-eating by spiders". Journal of Arachnology. 44: 15–27. doi:10.1636/P15-45.1 – via ORCA.
- Pappas, Stephanie (March 15, 2016). "These Spiders Like Some Greens with Their Insects". Live Science.
- Harmon, Katherine (October 12, 2009). "Unusual Spider Species Passes Up Live Prey for Plants". Scientific American.
- Meehan, C.J.; Olson, E.J.; Reudink, M.W.; Kyser, T.K.; Curry, R.L. (2009). "Herbivory in a spider through exploitation of an ant–plant mutualism". Current Biology. 19 (19): R892–3. doi:10.1016/j.cub.2009.08.049. PMID 19825348.
- Yeargan, K.V. and Quate, L.W., (1997). Adult male bolas spiders retain juvenile hunting tactics. Oecologia 112: 572–576. doi = 10.1007/s004420050347
- Barbour, T (1921). "Spiders feeding on small cyprinodonts" (PDF). Psyche. 28 (4): 131–132. doi:10.1155/1921/19421.
- University of Arkansas Museum Arthropod Museum web page: dark fishing spider (Dolomedes tenebrosus).
- Schütz, D.; Taborsky, M. (2003). "Adaptations to an aquatic life may be responsible for the reversed sexual size dimorphism in the water spider, Argyroneta aquatica" (PDF). Evolutionary Ecology Research. 5: 105–117. Archived from the original (PDF) on 2008-12-16.
- Murphy, F. and Murphy, J., (2000). An Introduction to the Spiders of South East Asia. Malaysian Nature Society, Kuala Lumpur.
- Levi, H.W. (1993). "The orb-weaver genus Kaira (Araneae: Araneidae)" (PDF). Journal of Arachnology. 21: 209–225.
- Foelix, Rainer F. Biology of Spiders, 1982.
- Roberts, Michael J. Spiders of Britain and Northern Europe, Collins, London, 1995.
- Dolores Schütz & Michael Taborsky (2005). "Mate choice and sexual conflict in the size dimorphic water spider Argyroneta aquatica (Araneae: Argyronetidae)" (PDF). Journal of Arachnology. 33 (3): 767–775. doi:10.1636/S03-56.1.
- Johnson, J.; Andrew Sih (August 2005). "Precopulatory sexual cannibalism in fishing spiders (Dolomedes triton): A role for behavioral syndromes". Behavioral Ecology and Sociobiology. 58 (4): 390–396. CiteSeerX 10.1.1.630.9443. doi:10.1007/s00265-005-0943-5.
- Hansen, L.S.; Gonzales, S.F.; Toft, S.; Bilde, T. (2008). "Thanatosis as an adaptive male mating strategy in the nuptial gift–giving spider Pisaura mirabilis". Behavioral Ecology. 19 (3): 546–551. CiteSeerX 10.1.1.507.7843. doi:10.1093/beheco/arm165.
- Wilder, Shawn M.; Rypstra, Ann L. (2008). "Sexual Size Dimorphism Predicts the Frequency of Sexual Cannibalism Within and Among Species of Spiders". The American Naturalist. 172 (3): 431–440. doi:10.1086/589518. PMID 18616388.
- Vollrath, F (1986). "Eusociality and extraordinary sex ratios in the spider Anelosimus eximius (Araneae: Theridiidae)". Behavioral Ecology and Sociobiology. 18 (4): 283–287. doi:10.1007/BF00300005.
- Agnarsson, I.; Aviles, L.; Coddington, J.A.; Maddison, W.P. (2006). "Sociality in Theridiid spiders: Repeated origins of an evolutionary dead end". Evolution. 60 (11): 2342–51. doi:10.1554/06-078.1. PMID 17236425.
- Rypstra, A.L. (1993). "Prey size, social competition, and the development of reproductive division of labor in social spider groups". The American Naturalist. 142 (5): 868–880. doi:10.1086/285577.
- Parry, D.A.; Brown, R.H.J. (1959). "The hydraulic mechanism of the spider leg". Journal of Experimental Biology. 36: 423–433.
- Ruppert, E.E., Fox, R.S. and Barnes, R.D., (2004). Invertebrate Zoology (7 ed.). Brooks/Cole. ISBN 0-03-025982-7
- Weihmann, T.; Günther, M.; Blickhan, R. (2012). "Hydraulic leg extension is not necessarily the main drive in large spiders". The Journal of Experimental Biology. 215 (4): 578–583. doi:10.1242/jeb.054585. PMID 22279064.
- Weyman, G.S. (1995). "Laboratory studies of the factors stimulating ballooning behavior by Linyphiid spiders (Araneae, Linyphiidae)". The Journal of Arachnology. 23: 75–84.
- Schneider, J.M.; Roos, J.; Lubin, Y.; Henschel, J.R. (2001). "Dispersal of Stegodyphus Dumicola (Araneae, Eresidae): They do balloon after all!" (PDF). The Journal of Arachnology. 29: 114–116. doi:10.1636/0161-8202(2001)029[0114:DOSDAE]2.0.CO;2.
- Bond, J.E. (1999). "Systamatic and evolution of the Californian trapdoor spider genus Aptostichus Simon (Araneae: Mygalomorphae: Euctenizidae)" (PDF). Virginia Polytechnic Institute and State University. Retrieved April 19, 2013.
- Eisner, T.; Camazine, S. (1983). "Spider leg autotomy induced by prey venom injection: An adaptive response to 'pain'?". Proceedings of the National Academy of Sciences. 80 (11): 3382–3385. doi:10.1073/pnas.80.11.3382. PMC 394047. PMID 16593325.