Portia is a genus of jumping spider that feeds on other spiders (i.e., they are araneophagic or arachnophagic). They are remarkable for their intelligent hunting behaviour, which suggests that they are capable of learning and problem solving, traits normally attributed to much larger animals.[2]
The genus was established in 1878 by German arachnologist Friedrich Karsch. The fringed jumping spider (Portia fimbriata) is the type species.[1]
Molecular phylogeny, a technique that compares the DNA of organisms to construct the tree of life, indicates that Portia is a member of a basal clade (i.e. quite similar to the ancestors of all jumping spiders) and that the Spartaeus, Phaeacius, and Holcolaetis genera are its closest relatives.[3]
Wanless divided the genus Portia into two species groups: the schultzi group, in which males' palps have a fixed tibialapophysis; and the kenti group, in which the apophysis of each palp in the males has a joint separated by a membrane.[4] The schultzi group includes P. schultzi, P. africana, P. fimbriata, and P. labiata.[4]
At least some species of Portia are in the state of reproductive isolation: in a laboratory, male P. africana copulated with female P. labiata, but no eggs were laid; during all cases, the female P. labiata twisted and lunged in an attempt to bite.[5]:435-466
Some specimens found trapped in Oligoceneamber were identified as related to Portia.[6]
Portia are vulnerable to larger predators such as birds and frogs, which a Portia often cannot identify because of the predator's size.[7] Some insects prey on Portia, for example, mantises, the assassin bugsNagusta sp. indet. and Scipinnia repax (that is, Scipinia rapax [8]).[9]
Appearance
Portia are relatively small spiders. For example, adult females of Portia africana are 5 to 10 millimetres (1⁄5 to 2⁄5in) in body length and adult males are 5 to 7 millimetres (1⁄5 to 3⁄10in) long.[10]
Intelligence
Portia often hunt in ways that seem intelligent.[11] All members of Portia have instinctive hunting tactics for their most common prey, but can improvise by trial and error against unfamiliar prey or in unfamiliar situations, and then remember the new approach.[7]
They exhibit spatial memory and object permanence,[12][13] and are capable of trying out a behavior to obtain feedback regarding success or failure, and they can plan ahead (as it seems from their detouring behavior).[14]
Portia species can make detours to find the best attack angle against dangerous prey, even when the best detour takes a Portia out of visual contact with the prey,[7] and sometimes the planned route leads to abseiling down a silk thread and biting the prey from behind. Such detours may take up to an hour,[15] and a Portia usually picks the best route even if it needs to walk past an incorrect route.[16]:422
Nonetheless, they seem to be relatively slow thinkers, as is to be expected since they solve tactical problems by using brains vastly smaller than those of mammalian predators.[11]Portia has a brain significantly smaller than the size of the head of a pin,[17] and it likely has less than 100,000 neurons[18] (for comparison, a mouse brain has about 70 million neurons[19] and a human brain has 86 billion[20]).
Portia can distinguish their own draglines from conspecifics', recognizing self from others, and also discriminate between known and unknown spiders.[21]
Hunting techniques
Their favorite prey appears to be web-building spiders between 10% and 200% of their own size. Portia looks like leaf detritus caught in a web, and this is often enough to fool web-building spiders, which have poor eyesight.[11]
When stalking web-building spiders, Portia try to make different patterns of vibrations in the web that aggressively mimic the struggle of a trapped insect or the courtship signals of a male spider, repeating any pattern that induces the intended prey to move towards the Portia.[22]Portia fimbriata has been observed to perform vibratory behavior for three days until the victim decided to investigate.[23] They time invasions of webs to coincide with light breezes that blur the vibrations that their approach causes in the target's web; and they back off if the intended victim responds belligerently. Other jumping spiders take detours, but Portia is unusual in its readiness to use long detours that break visual contact.[22]
Female P. fimbriata in a web
Laboratory studies show that Portia learns very quickly how to overcome web-building spiders that neither it nor its ancestors would have met in the wild. Portia's accurate visual recognition of potential prey is an important part of its hunting tactics. For example, in one part of the Philippines, local Portia spiders attack from the rear against the very dangerous spitting spiders, which themselves hunt jumping spiders. This appears to be an instinctive behavior, as laboratory-reared Portia of this species do this the first time they encounter a spitting spider. On the other hand, they will use a head-on approach against spitting spiders that are carrying eggs. However, experiments that pitted Portia against "convincing" artificial spiders with arbitrary but consistent behavior patterns showed that Portia's instinctive tactics are only starting points for a trial-and-error approach from which these spiders learn very quickly.[22]
Against other jumping spiders, which also have excellent vision, Portia may mimic fragments of leaf litter detritus. When close to biting range, Portia use different combat tactics against different prey spiders. On the other hand, when attacking unarmed prey, such as flies, they simply stalk and rush,[24] and they also capture prey by means of sticky webs.[22]
Portia can also rely on movement cues to locate prey. In this specific strategy, when potential prey knows it's been seen and stands still to avoid detection, undirected leaps occur in the vicinity of the prey. As a result, the prey will then react to this visual cue, believing itself to have been seen, providing motion that allows Portia to see and attack it.[25]
Portia may also scavenge corpses of dead arthropods they found,[26] and consume nectar.[27]
Social behavior
Members of the species Portia africana were observed living together and sharing prey.[28]
If a mature Portia male meets a sub-mature female, he will try to cohabitate with her.[5]:467
P. labiata females can discriminate between the draglines of familiar and unfamiliar individuals of the same species[29] and between their own draglines and those of conspecifics.[30] The ability to recognize individuals is a necessary prerequisite for social behavior.[31]
Vision
Eyes of Portia schultzi
Diagram of the visual fields of the spider as viewed from above
Portia species have complex eyes that support exceptional spatial acuity.[32][33] They have eight eyes. Three pairs of eyes positioned along the sides of the cephalothorax (called the secondary eyes) have a combined field-of-view of almost 360° and serve primarily as movement detectors. A pair of forward-facing anterior median eyes (called the principal eyes) are adapted for colour vision and high spatial acuity.[34]
The main eyes focus accurately on an object at distances from approximately 2 centimetres (0.79in) to infinity,[35][36] and in practice can see up to about 75 centimetres (30in).[35]:53 Like all jumping spiders, its main eyes can take in only a small visual field at one time,[37] as the most acute part of a main eye can see all of a circle up to 12 millimetres (1⁄2in) wide at 20 centimetres (8in) away, or up to 18 millimetres (3⁄4in) wide at 30 centimetres (12in) away.[38] Jumping spiders' main eyes can see from red to ultraviolet.[39]
The secondary eyes have low spatial resolving power, but a wide field of view.[40]
The inter-receptor angles of Portia's eyes may be as small as 2.4 minutes of arc, which is only six times worse than in humans, and is six times better than in the most acute insect eye.[41] It is also clearer in daylight than a cat's vision.[7]
P. africana relies on visual features of general morphology and colour (or relative brightness) when identifying prey types.[42]P. schultzi's hunting is stimulated only by vision, and prey close by but hidden causes no response.[43]P. fimbriata use visual cues to distinguish members of the same species from other salticids.[44]
Cross and Jackson (2014) suggest that P. africana is capable of mentally rotating visual objects held in its working memory.[42]
However, a Portia takes a relatively long time to see objects, possibly because getting a good image out of such small eyes is a complex process and requires a lot of scanning.[e] This makes a Portia vulnerable to much larger predators such as birds, frogs and mantises, which a Portia often cannot identify because of the predator's size.[7]
When not hunting for prey or a mate, Portia species adopt a special posture, called the "cryptic rest posture", pulling their legs in close to the body and their palps back beside the chelicerae ("jaws"), which obscures the outlines of these appendages. When walking, most Portia species have a slow, "choppy" gait that preserves their concealment: pausing often and at irregular intervals; waving their legs continuously and their palps jerkily up and down; moving each appendage out of time with the others;[45][46] and continuously varying the speed and timing.[16]
When disturbed, some Portia species are known to leap upwards about 100 to 150 millimetres (4 to 6in) often from the cryptic rest pose, and often over a wide trajectory. Usually the spider then either freezes or runs about 100 millimetres (4in) and then freezes.[5]
Portia exhibits a mating behavior and strategy different from that of other jumping spiders. In most jumping spiders, males mount females to mate. The Portia male shows off his legs and extends them stiffly and shakes them to attract the female.[47] The female then drums on the web. After the male mounts her, the female drops a dragline and they mate in mid-air. Mating with Portia spiders can occur off or on the web. The spider also practices cannibalism before and after copulation. The female usually twists and lunges at the mounted male. (P. fimbriata, however, is an exception; it does not usually exhibit such behavior.) If the male is killed before completing copulation, the male sperm is removed and the male is then eaten. If the male finishes mating before being killed, the sperm is kept for fertilization and the male is eaten. A majority of males are killed during sexual encounters.
Health
Portia species have a life span of about 1.5 years.[48]
P. fimbriata can regenerate a lost limb about 7 days after moulting.[49]
Portia's palps and legs break off very easily, which may be a defense mechanism, and Portias are often seen with missing legs or palps.[26]
Species
As of October2022[update] it contains 21 species, found in Africa, Asia, and Australia:[1]
Trial and error is a fundamental method of problem-solving characterized by repeated, varied attempts which are continued until success, or until the practicer stops trying.
Jumping spiders are a group of spiders that constitute the family Salticidae. As of 2019, this family contained over 600 described genera and over 6,000 described species, making it the largest family of spiders at 13% of all species. Jumping spiders have some of the best vision among arthropods and use it in courtship, hunting, and navigation. Although they normally move unobtrusively and fairly slowly, most species are capable of very agile jumps, notably when hunting, but sometimes in response to sudden threats or crossing long gaps. Both their book lungs and tracheal system are well-developed, and they use both systems. Jumping spiders are generally recognized by their eye pattern. All jumping spiders have four pairs of eyes, with the anterior median pair being particularly large.
Portia labiata is a jumping spider found in Sri Lanka, India, southern China, Burma (Myanmar), Malaysia, Singapore, Java, Sumatra and the Philippines. In this medium-sized jumping spider, the front part is orange-brown and the back part is brownish. The conspicuous main eyes provide vision more acute than a cat's during the day and 10 times more acute than a dragonfly's, and this is essential in P. labiata′s navigation, hunting and mating.
Phidippus audax, the Bold jumper or Daring jumping spider, is a common species of spider belonging to the genus Phidippus, a group of jumping spiders easily identified by their large eyes and their iridescent chelicerae. Like all jumping spiders, they have excellent stereoscopic vision that aids them in stalking prey and facilitates visual communication with potential mates during courting. Bold jumping spiders are native to North America and have been introduced to Hawaii, Nicobar Islands, Azores, and the Netherlands. They are typically black with a distinct white triangle on their abdomen.
Brettus is a genus of jumping spiders. Its six described species are found in southern Asia from India to China and Sulawesi, with a single species endemic to Madagascar.
Cocalus is a genus of jumping spiders that was first described by Carl Ludwig Koch in 1846, and is named after Cocalus, a Sicilian king of Greek mythology.
Phaeacius is a spider genus of the family Salticidae, found in sub-tropical China and between India and the Malay Peninsula, including Sri Lanka, Sumatra and the Philippines. Although other spiders can jump, salticids including Phaeacius have significantly better vision than other spiders, and their main eyes are more acute in daylight than a cat's and 10 times more acute than a dragonfly's. The main eyes focus accurately on an object at distances from approximately 2 centimetres (0.79 in) to infinity, and in practice can see up to about 75 centimetres (30 in). They do not spin webs.
Evarcha culicivora is a species of jumping spider found only around Lake Victoria in Kenya and Uganda. At maturity, E. culicivora spiders have an average size of 5 mm for both males and females. The range in size for either sex is quite small, with females being only slightly larger on average.
Maevia inclemens or the dimorphic jumping spider is a relatively common and colorful jumping spider of North America. In the males there are two forms, a very rare phenomenon in zoology. These use different courting displays, and differ in appearance: the "tufted" morph has a black body and pedipalps ("palps"), three black tufts across its "head", and pale legs; and the "gray" morph has black and white stripes all over its body and legs, orange palps, and no tufts. However, each form accounts for 50% of the adult males, and they are equally successful in mating. A female of Maevia inclemens is 6.5 to 8.0 millimetres long, while males are 4.75 to 6.50 millimetres long.
Pholcus phalangioides, commonly known as the cosmopolitan cellar spider, long-bodied cellar spider, house ghost spider or one of various types called a daddy long-legs spider, is a spider of the family Pholcidae. This is the only spider species described by the Swiss entomologist Johann Kaspar Füssli, who first recorded it in 1775. Its common name of "daddy long-legs" should not be confused with a different arachnid group with the same common name, the harvestman (Opiliones), or the crane flies of the superfamily Tipuloidea.
Trite planiceps, commonly known as the black-headed jumping spider, is a common jumping spider (Salticidae) endemic to New Zealand and one of about 150 species of jumping spiders in New Zealand.
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 September 2024, 52,309 spider species in 134 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.
Portia fimbriata, sometimes called the fringed jumping spider, is a jumping spider found in Australia and Southeast Asia. Adult females have bodies 6.8 to 10.5 millimetres long, while those of adult males are 5.2 to 6.5 millimetres long. Both sexes have a generally dark brown carapace, reddish brown chelicerae ("fangs"), a brown underside, dark brown palps with white hairs, and dark brown abdomens with white spots on the upper side. Both sexes have fine, faint markings and soft fringes of hair, and the legs are spindly and fringed. However, specimens from New Guinea and Indonesia have orange-brown carapaces and yellowish abdomens. In all species of the genus Portia, the abdomen distends when the spider is well fed or producing eggs.
Portia schultzi is a species of jumping spider which ranges from South Africa in the south to Kenya in the north, and also is found in West Africa and Madagascar. In this species, which is slightly smaller than some other species of the genus Portia, the bodies of females are 5 to 7 mm long, while those of males are 4 to 6 mm long. The carapaces of both sexes are orange-brown with dark brown mottling, and covered with dark brown and whitish hairs lying over the surface. Males have white tufts on their thoraces and a broad white band above the bases of the legs, and these features are less conspicuous in females. Both sexes have tufts of orange to dark orange above the eyes, which are fringed with pale orange hairs. Males' abdomens are yellow-orange to orange-brown with blackish mottling, and on the upper sides are black and light orange hairs, and nine white tufts. Those of females are pale yellow and have black markings with scattered white and orange-brown hairs on the upper side. P. schultzi has relatively longer legs than other Portia, and a "lolloping" gait.
Portia africana is a jumping spider found in Angola, Cameroon, the Central African Republic, Gabon, Ghana, the Ivory Coast, Sierra Leone, Zaire and Zambia. Its conspicuous main eyes provide vision more acute than a cat's during the day and 10 times more acute than a dragonfly's, and this is essential in P. africana′s navigation, hunting and mating.
Holocnemus pluchei, commonly known as the marbled cellar spider, is a species of Pholcidae, a family commonly referred to as "cellar spiders" or "daddy long-legs". This species is distributed across the North Pacific region of the United States, as well as in parts of North Africa, Europe, and the Mediterranean. It is considered a common household spider and builds its nest in attics, basements, and eaves of houses. Although some members of the species live in solitary webs, the majority join already existing webs and migrate to new webs multiple times throughout the course of their lives. A unique feature of H. pluchei is that while in many species of spiders, stridulation commonly occurs by males during sexual encounters, in H. pluchei, females also possess stridulatory organs, and both sexes engage in stridulation.
Brettus adonis, is a species of spider of the genus Brettus. It is endemic to Sri Lanka.
Brettus cingulatus is a species of jumping spider of the genus Brettus. It is found in Myanmar and India.
Maratus griseus, the white-banded house jumping spider, is a species of jumping spider in the family Salticidae. It is found in Australia and New Zealand.
Maevia intermedia is one of eight species of Salticidae, or jumping spider, in the genus Maevia, and is native to North America. This species was originally reported by American Zoologist Robert D. Barnes in 1955 as a needed distinguishment between the similar-looking Maevia species, especially those found in the Americas.
↑ "Archived copy"(PDF). agro.icm.edu.pl. Archived from the original(PDF) on 10 June 2016. Retrieved 22 May 2022.{{cite web}}: CS1 maint: archived copy as title (link)
↑ "Scipinia is a genus of true bugs in the family assassin bugs." Encyclopedia of Life. Scipinia Stål 1861. Scipinia rapax Miller 1941. https://eol.org/pages/9003840
↑ Wilcox, S. & Jackson, R. (2002). "Jumping Spider Tricksters"(PDF). In Bekoff, M.; Allen, C. & Burghardt, G.M. (eds.). The Cognitive Animal: Empirical and Theoretical Perspectives on Animal Cognition. MIT Press. pp.27–34. ISBN978-0-262-52322-6. Archived from the original(PDF) on 2011-07-21. Retrieved 12 May 2011.
↑ Barrett, Louise (24 April 2011). "The Implausible Nature of Portia". Beyond The Brain: How Body and Environment Shape Animal and Human Minds. Princeton, New Jersey 08540: Princeton University Press. p.60. ISBN978-0-691-12644-9.{{cite book}}: CS1 maint: location (link)
↑ Harland, D.P. & Jackson, R.R. (April 2006). "A knife in the back: use of prey-specific attack tactics by araneophagic jumping spiders (Araneae: Salticidae)". Journal of Zoology. 269 (3): 285–290. doi:10.1111/j.1469-7998.2006.00112.x.
↑ Clark, R. J.; Harland, D. P.; Jackson, R.R (2000). "Speculative hunting by an araneophagic salticid Spider". Behaviour. 137 (12): 1601–1612. doi:10.1163/156853900502736.
↑ Jackson, Robert R.; Pollard, Simon D.; Salm, Kathryn (2008). "Observations of Portia Africana , an araneophagic jumping spider, living together and sharing prey". New Zealand Journal of Zoology. 35 (3): 237–242. doi:10.1080/03014220809510119. S2CID84796264.
↑ Clark, R.J.; Jackson, R.R. (1995). "Araneophagic jumping spiders discriminate between the draglines of familiar and unfamiliar conspecifics". Ethology Ecology & Evolution. 7 (2): 185–190. Bibcode:1995EtEcE...7..185C. doi:10.1080/08927014.1995.9522964.
↑ Clark, R.J.; Jackson, R.R. (1994). "Self recognition in a jumping spider: Portia labiata females discriminate between their own draglines and those of conspecifics". Ethology Ecology. 6 (3): 371–375. Bibcode:1994EtEcE...6..371C. doi:10.1080/08927014.1994.9522987.
↑ Harland, D.P.; Li, D.; Jackson, R.R. (2012). "How jumping spiders see the world". In Lazareva, O.; Shimizu, T.; Wasserman, E.A. (eds.). How animals see the world: comparative behavior, biology, and evolution of vision. New York: Oxford University Press. pp.133–164.
↑ Jackson, Robert R. (1982). "The biology of Portia fimbriata, a web-building jumping spider (Araneae, Salticidae) from Queensland: intraspecific interactions". Journal of Zoology. 196 (2): 295–305. doi:10.1111/j.1469-7998.1982.tb03505.x. ISSN0952-8369.
D.Harland and R.Jackson. Portia Perceptions: the Umwelt of an Araneophagic Jumping Spider / Complex Worlds from Simpler Nervous Systems. MIT Press, 2004 ISBN9780262162234
Harland, D.P & Jackson R.R. (2000): 'Eight-legged cats' and how they see - a review of recent research on jumping spiders (Araneae: Salticidae). Cimbebasia16: 231-240 PDF - vision and behavior in Portia spiders.
Harland, D.P.; Jackson, R.R. (2006). "A knife in the back: use of prey-specific attack tactics by araneophagic jumping spiders (Araneae: Salticidae)". Journal of Zoology. 269 (3): 285–290. doi:10.1111/j.1469-7998.2006.00112.x.
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