Portia Schultzi

''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 long, while those of males are 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.

While most jumping spiders focus accurately up to about away, ''P. schultzi'' responds to a maximum of about in good light, and ignores everything in very subdued light. For prey, ''P. schultzi'' prefers web-based spiders, then jumping spiders, and finally insects. The females of ''P. schultzi'' and other ''Portia'' species build "capture webs" to catch prey, and often join their own webs on to web-based spiders to catch the other spiders or their prey.

If a ''P. schultzi'' female is mature, a male ''P. schultzi'' will try to copulate with her, or cohabit with a subadult female and copulate while she is moulting. They usually mate on a web or on a dragline made by the female, and ''P. schultzi'' typically copulates for about 100 seconds, while others in the genus can take several minutes or even several hours. Females try to kill and eat their mates during or after copulation, and subadult females mimic adult females to attract males as prey. Contests between ''Portia'' females are violent, and embraces in ''P. schultzi'' typically take 20 to 60 seconds. Sometimes, one female knocks the other on her back and the other may be killed and eaten if she does not right herself quickly and run away. When hunting, ''P. schultzi'' mature females emit olfactory signals that reduce the risk that any other females, males, or juveniles of the same species may contend for the same prey.

Body structure and appearance

The bodies of female ''P. schultzi''s are 5 to 7 mm long (smaller than other ''Portia'' species), while those of males are 4 to 6 mm long. The carapaces of both sexes are orange-brown with dark brown mottling, and they are covered with dark brown and whitish hairs lying over the surface. Males have white tufts on their thoraxes and 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. Females' chelicerae are pale yellow with black markings at the ends, while males' are orange-brown with darker markings, and those of both sexes have pale orange and white hairs. The abdomens of females are pale yellow with black markings, and the upper sides have scattered white and orange-brown 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, but no tufts. The legs of both sexes are unusually long and slender, and those of males are orange-brown with darker markings while those of females are light yellow with blackish markings. In both sexes the final two segment of each leg has no other decorations, but the other segments in both sexes have brownish hairs and many robust spines, and those of males also have scattered white tufts. The palps of both sexes have pale yellow hairs and white fringes. All species of the genus '' Portia'' have elastic abdomens, so that those of both sexes can become almost spherical when well fed, and females' can stretch as much when producing eggs.

Movement

When not hunting for prey or a mate, ''Portia'' species, including ''P. schultzi'', 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, and continuously varying the speed and timing. ''P. schultzi'' uses what Forster and Murphy (1986) call a "lolloping" gait, flexing and stretching the legs. They suggest that the long legs are advantageous for moving through webs, and that lolloping enables ''P. schultzi'' to use the long legs while keeping the body near the surface.

Like many species of spider, a ''P. schultzi'' lays a continuous dragline of silk as it moves, and from time to time anchors the dragline to a surface with a spot of sticky silk. This allows the spider to return to the surface if the animal is dislodged. A spider about to jump first lays a sticky silk anchor, and then lays out a dragline as it flies. Unlike those of most jumping spiders, ''P. schultzi''′s draglines stick to each other and, when a ''P. schultzi'' has laid a few lines across a gap, it uses these as walkways and reinforces them with additional silk as it moves.

When disturbed, most leap upwards about 100 to 150 mm, often from the cryptic rest pose, and often over a wide trajectory. Usually ''Portia'' then either freezes or runs about 100 mm and then freezes.

Senses

Although other spiders can also jump, salticids including ''P. schultzi'' 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. Jumping spiders have eight eyes, the two large ones in the center-and-front position (the anteriomedian eyes, also called "principal eyes") housed in tubes in the head and providing acute vision. The other six are secondary eyes, positioned along the sides of the carapace and acting mainly as movement detectors. In most jumping spiders, the middle pair of secondary eyes is very small and has no known function, but those of ''Portia'' are relatively large, and function as well as those of the other secondary eyes. Jumping spiders' main eyes can see from red to ultraviolet.

In most jumping spiders, the main eyes focus accurately on an object up to about 75 cm away. However, ''P. schultzi'' does not react at all to objectives when the light is under 100 lux. Between 100 and 500 lux, it detects and approaches the objective from distances up to 6 cm, from 500 lux to 1500 lux, its response distance increases gradually to a maximum of about 10 cm, and stronger light causes no increase in the response distance. For comparison, ''Trite auricoma'' swivels towards a movement up to 75 cm away and approaches targets from about 20 cm. Perhaps ''P. schultzi'' gains little from being alerted to objectives at distances because this spider moves so slowly that it is very unlikely to reach a more distant target in time to catch it.

Like all jumping spiders, ''P. schultzi'' can take in only a small visual field at one time, as the most acute part of a main eye can see all of a circle up to 12 millimeters wide at 20 centimeters away, or up to 18 millimeters wide at 30 centimeters away. A ''Portia'' spider takes a relatively long time to see objects, possibly because getting a good image out of such tiny eyes is a complex process and needs a lot of scanning. This makes a ''Portia'' vulnerable to much larger predators such as birds, frogs, and mantises, which it often cannot identify because of the other predator's size.

Spiders, like other arthropods, have sensors, often modified setae (bristles), for smell, taste, touch and vibration protruding through their cuticle ("skin"). Unlike insects, spiders and other chelicerates do not have antennae. A ''Portia'' can sense vibrations from surfaces, and use these for mating and for hunting other spiders in total darkness. It can use air- and surface "smells" to detect prey which it often meets, to identify members of the same species, to recognise familiar members, and to determine the sex of other member of the same species.

Hunting tactics

Tactics used by most jumping spiders and by most of genus ''Portia''

Members of the genus ''Portia'' have hunting tactics as versatile and adaptable as a lion's. All members of ''Portia'' have instinctive 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. They can also make detours to find the best attack angle against dangerous prey, even when the best detour takes it out of visual contact with the prey, 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, and it usually picks the best route even if it needs to walk past an incorrect route. If a ''Portia'' spider makes a mistake while hunting another spider, it may itself be killed.

While most jumping spiders prey mainly on insects and by active hunting, females of ''Portia'' also build webs to catch prey directly. These "capture webs" are funnel-shaped and widest at the top and are about 4,000 cm³ in volume. The web is initially built in about 2 hours, and then gradually made stronger. A ''Portia'' spider often joins her own web on to one of a web-based nonsalticid spider. When not joined to another spiders', a ''P. schultzi'' female's capture web may be suspended from rigid foundations such as boughs and rocks, or from pliant bases such as stems of shrubs. Males of ''Portia'' do not build capture webs.

''Portia''s hunt in all types of webs, while other cursorial spiders generally have difficulty moving on webs, and web-building spiders find it difficult to move in webs unlike those they build. Where the web is sparse, a ''Portia'' will use "rotary probing", in which it moves a free leg around until it meets a thread. When hunting in another spider's web, a ''Portia''′s slow, choppy movements and the flaps on its legs make it resemble leaf detritus caught in the web and blown in a breeze. ''P. schultzi'' and some other ''Portia''s use breezes and other disturbances as "smokescreens" in which these predators can approach web spiders more quickly, and revert to a more cautious approach when the disturbance disappears. A few web spiders run far away when they sense the un-rhythmical gait of a ''Portia'' entering the web - a reaction Wilcox and Jackson call "''Portia'' panic".

If a large insect is struggling in a web, ''Portia'' usually does not usually take the insect, but waits for up to a day until the insect stops struggling, even if the prey is thoroughly stuck. When an insect stuck in a web owned by ''P. schultzi'', '' P. labiata'' or any regional variant of '' P. fimbriata'', and next to a web spider's web, the web spider sometimes enters the ''Portia''′s web, and the ''Portia'' pursues and catches the web spider.

The webs of spiders on which ''Portia''s prey sometimes contain dead insects and other arthropods which are uneaten or partly eaten. ''P. schultzi'' and some other ''Portia''s such as ''P. fimbriata'' (in Queensland) and ''P. labiata'' sometimes scavenge these corpses if the corpses are not obviously decayed.

A ''Portia'' typically takes 3 to 5 minutes to pursuit prey, but some pursuits can take much longer, and in extreme cases close to 10 hours when pursuing a web-based spider.

All ''Portia''s eat eggs of other spiders, including eggs of their own species and of other cursorial spiders, and can extract eggs from cases ranging from the flimsy ones of ''Pholcus'' to the tough papery ones of '' Philoponella''. While only ''P. fimbriata'' (in Queensland) captures cursorial spiders in their nests, all ''Portia''s steal eggs from empty nests of cursorial spiders.

''Portia''s' venom is unusually powerful against spiders. When a ''Portia'' stabs a small to medium spider (up to the ''Portia''′s weight), including another ''Portia'', the prey usually runs away for about 100 to 200 millimetres, enters convulsions, becomes paralysed after 10 to 30 seconds, and continues convulsing for 10 seconds to 4 minutes. ''Portia'' slowly approaches the prey and takes it. ''Portia'' usually needs to inflict up to 15 stabbings to completely immobilise a larger spider(1.5 to 2 times to the ''Portia''′s weight), and then ''Portia'' may wait about 20 to 200 millimetres away for 15 to 30 minutes from seizing the prey. Insects are usually not immobilised so quickly but continue to struggle, sometimes for several minutes. If ''Portia'' cannot make further contact, all types of prey usually recover, making sluggish movements several minutes after the stabbing but often starting normal movement only after an hour.

Occasionally a ''Portia'' is killed or injured while pursuing prey up to twice ''Portia''′s size. In tests, ''P. schultzi'' is killed in 1.7% of pursuits and injured but not killed in 5.3%, ''P. labiata'' is killed in 2.1% and injured but not killed in 3.9%, and ''P. fimbriata'' in Queensland is killed in 0.06% of its pursuits and injured but not killed in another 0.06%. A ''Portia''′s especially tough skin often prevents injury, even when its body is caught in the other spider's fangs. When injured, ''Portia'' bleeds and may sometimes loses one or more legs. Spiders' palps and legs break off easily when attacked, ''Portia''′s palps and legs break off exceptionally easily, which may be a defence mechanism, and ''Portia''s are often seen with missing legs or palps, while other salticids in the same habitat are not seen with missing legs or palps.

Tactics used by ''Portia schultzi''

All performance statistics summarise result of tests in a laboratory, using captive specimens. The following table shows the hunting performance of adult females. In addition to ''P. schultzi'', the table shows for comparison the hunting performances of '' P. africana'', '' P. labiata'' and three regional variants of '' P. fimbriata''.

Notes on this table:

* "Tendency to pursue prey" is the percentage of tests in which the subject pursues the potential prey, and a pursuit starts when the ''Portia'' either approaches the prey or shakes the prey's web.
* "Efficiency in capturing prey" is the percentage of pursuits in which the subject captures the prey.
* ''P. schultzi'' specimens from Kenya were used in this analysis.
* "(Q)", "(NT)" and "(SL)" identify ''P. fimbriata''s from Queensland, Northern Territory and Sri Lanka.
* The prey used were: unspecified jumping spiders; amaurobiid and theridiid web-based spiders; and houseflies.

For resting, all ''Portia''s spin a horizontal web whose diameter is about twice the spider's body length and is suspended only 1 to 4 millimetres below a leaf. ''P. schultzi'' returns to its resting platform at night. While eating prey at dusk and with no platform nearby, one ''P. schultzi'' built a silk platform while holding the prey, and then continued eating.

''P. schultzi'' does not respond to prey if the light is under 100 lux (like a restaurant with only subdued artificial lighting), but responds to prey at distances from 6 to 10 centimetres as the light level increases. A test suggested that ''P. schultzi''′s hunting is stimulated only by vision, as prey close but hidden caused no response. A preliminary check showed that lures got the same responses from ''P. schultzi'' as live prey, and then more detailed testing with the lures showed that: if the target moved erratically, ''P. schultzi'' did not pursue it; if the target was totally stationary, the spider approached very slow (between 5 and 100 millimetres per minute), with very long pauses in the final stages, and the sequence was not completed in 43% of cases; if the lure jiggled on the same spot, ''P. schultzi'' approached much faster and the sequence was almost always completed; if a lure was pulled directly away from ''P. schultzi'', the spider followed, and faster if the lure was pulled, up to a limit (''P. schultzi'' generally moves very slowly).

A female ''P. schultzi'' more often pursues small jumping spiders and web spiders than larger prey. While it more often catches small jumping spiders than larger ones, it is about equally effective with all sizes of web spiders up to twice ''P. schultzi''′s size. A female ''P. schultzi'' is effective against insects up to twice ''P. schultzi''′s size when the insect is stuck in a non-salticid's web, and against insects not in webs and up to ''P. schultzi''′s size, while ''P. schultzi'' seldom pursues or catches a larger insect in the open. A female ''P. schultzi'' very seldom pursues or catches a larger insect in her own web, and is slightly less effective against smaller insects in ''P. schultzi''′s web than in other situations. Males are less efficient in all cases.

A test in 1997 showed that ''P. schultzi''′s preferences for different types of prey are in the order: web spiders; jumping spiders; and insects. These preferences apply to both live prey and motionless lures, and to ''P. schultzi'' specimens without prey for 7 days ("well-fed") and without prey for 14 days ("starved"). ''P. schultzi'' specimens without prey for 21 days ("extra-starved") showed no preference for different types of prey. The test included as prey several species of web spiders and jumping spiders, and the selection of the prey species showed no evidence of affecting the results. Insects were represented by the house fly '' Musca domestica''.

In a test, ''P. schultzi'' spiderlings took Drosophila ("fruit flies") almost as often as spiders. ''P. schultzi'' retreats from the sudden flights of houseflies found in the open, but sometimes takes flies entangled in a web. Out of its web, ''P. schultzi'' rarely capture thomisids (non-web sit-and-wait predators, usually under 13 millimetres long ) in the open, as thomisids often wave their front legs when threatened.

If a spider walks under a ''P. schultzi'' female's capture web and the vertical distance is less than 8 centimetres, the ''P. schultzi'' often drops onto the prey too fast for a human eye to follow. If the ''P. schultzi'' misses, it quickly returns up its safety line to its vantage point and looks for another chance - and seldom misses the second time. Most drops cover two to four centimetres, as longer drops are often obstructed by the web.

When hunting a web spider in the prey's web, a ''P. schultzi'' walks very slowly towards the prey and then, when two to three centimetres away, pauses for some minutes. During this time the ''P. schultzi'' quivers very quickly with its whole body at regular intervals. In almost all cases the prey stays motionless. ''P. schultzi'' never plucks the web as ''Portia fimbriata'' does.

Unlike the Queensland variant of ''P. frimbriata'', ''P. schultzi'' has no special tactics when hunting other jumping spiders.

When hunting, mature females of ''P. fimbriata'', ''P. africana'', ''P. fimbriata'', ''P. labiata'', and ''P. schultzi'' emit olfactory signals that reduce the risk that any other females, males or juveniles of the same species may contend for the same prey. The effect inhibits aggressive mimicry against a prey spider even if the prey spider is visible, and also if the prey is inhabiting any part of a web. If a female of one of these ''Portia''s smells a male of the same species, the female stimulates the males to court. These ''Portia'' species do not show this behaviour when they receive olfactory signals from members of other ''Portia'' species.

Reproduction and lifecycle

Before courtship, a male ''Portia'' spins a small web between boughs or twigs, and he hangs under that and ejaculates on to it. He then soaks the semen into reservoirs on his pedipalps, which are larger than those of females. Females of many spider species, including ''P. schultzi'', emit volatile pheromones into the air, and these generally attract males from a distance.

Among ''P. schultzi'' and some other ''Portia''s, when adults of the same species but opposite sexes recognise each other, they display at 10 to 30 centimetres. Males usually wait for 2 to 15 minutes before starting a display, but sometimes a female starts a display first. ''Portia''s sometimes use "propulsive displays", with which a member threatens a rival of the same species and sex, and unreceptive females also threaten males in this way. A propulsive display is a series of sudden, quick movements including striking, charging, ramming and leaps. In ''P. schultzi'' and in some other species, contests between males usually last only 5 to 10 seconds, and only their legs make contact. Contests between ''Portia'' females are violent and embraces in ''P. schultzi'' typically take 20 to 60 seconds. These occasionally include grappling that sometimes breaks a leg, but more usually the final move is a lunge. Sometimes one knocks the other on her back and the other may be killed and eaten if she does not right herself quickly and run away. If the loser has a nest, the winner takes over and eats any eggs there.

A female ''P. schultzi'' that sees a male may approach slowly or wait. The male then walks erect and displaying by waving his legs and palps. If the female does not run away, she gives a propulsive display first. If the male stands his ground and she does not run away or repeat the propulsive display, he approaches and, if she is mature, they copulate. If the female is sub-adult (one moult from maturity), a male may cohabit in the female's capture web. ''Portia''s usually mate on a web or on a dragline made by the female. ''P. schultzi'' typically copulates for about 100 seconds, while other genera can take several minutes or even several hours.

Females of ''P. schultzi'', like those of '' P. labiata'', try to kill and eat their mates during or after copulation, by twisting and lunging. The males wait until the females have hunched their legs, making this attack less likely. Males also try to abseil from a silk thread to approach from above, but females may manoeuvre to get the higher position. If the female moves at all, the male leaps and runs away.

Before being mature enough to mate, females of ''P. shultzi'' and also ''P. labiata'' mimic adult females to attract males as prey.

''P. schultzi'' usually lays eggs on dead, brown leaves about 20 millimetres long, suspended near the top of its capture web, and then cover the eggs with a sheet of silk. If there is no dead leaf available, the female will make a small horizontal silk platform in the capture web, lay the eggs on it, and then cover the eggs. ''P. schultzi'' has been seen laying eggs in a rolled-up leaf in a web of ''Ischnothele karschi''.

For moulting, all ''Portia''s spin a horizontal web whose diameter is about twice the spider's body length and is suspended only below a leaf. The spider lies head down, and often slides down during moulting. ''Portia''s spin a similar temporary web for resting. Like all arthropods, spiders moult and, after hatching, the life stage before each moult is called an "instar". The distinctive tufts of ''P. schultzi'' juveniles appear in the third instar.

''P. schultzi'' exuviae (discarded "skins") have been found both in their own webs and in those of ''I. karschi'', which has suggested that ''P. schultzi'' moults in the open. In one case, while its new skin was still pale and soft, its spinnerets were still stuck in the discarded skin, and the spider slowly twirled for about 90 seconds until it was free. The spider's body then darkened quickly to the normal colouration, and some time later the spider hung in its usual upside-down posture in the web.

Ecology

''P. schultzi''′s range runs from Durban (in South Africa) in the south to Malindi (in Kenya) in the north, and westwards to the East African Rift, and also in West Africa and Madagascar.

''P. schultzi'', along with a large variety of spiders and insects, is often found in the dense, large webs of the diplurid ''Ischnothele karschi'' (about 15 millimetres long), which are especially abundant in partly cleared secondary bush where rain forests have been cut down, and usually about one metre above the ground. A survey of one area suggested that there is about one ''P. schultzi'' per three ''I. karschi'' webs. ''P. schultzi'' is also found in its own web and those of other spiders, on tree trunks and the walls of buildings, and in leaf litter.

Taxonomy

''P. schultzi'' is one of 17 species in the genus '' Portia'' as of June 2011. ''Portia schultzi'' Karsch, 1878 is synonymous with ''Brettus martini'' Simon, 1900, ''Linus lesserti'' Lawrence, 1937 and ''Linus alboguttatus'' Lawrence, 1938.

Wanless divided the genus ''Portia'' into two species groups: the ''schultzi'' group, in which males' palps have a fixed tibial apophysis; and the ''kenti'' group, in which the apophysis of each palp in the males has a joint separated by a membrane. The ''schultzi'' group includes ''P. schultzi'', ''P. africana'', '' P. fimbriata'', and '' P. labiata''.

''Portia'' is in the subfamily Spartaeinae, which is thought to be primitive. Molecular phylogeny, a technique that compares the DNA of organisms to reconstruct the tree of life, indicates that ''Portia'' is a member of the clade Spartaeinae, that Spartaeinae is basal (quite similar to the ancestors of all jumping spiders), that ''Portia''′s closest relative is the genus '' Spartaeus'', and that the next closest are ''Phaeacius'' and ''Holcolaetis''.

Notes

References

External links

Salticidae: Diagnostic Drawings Library - Portia schultzi
by Jerzy Proszynski.

{{Taxonbar, from=Q2702827

Salticidae
Spiders of Africa
Spiders described in 1878
Taxa named by Ferdinand Karsch