Katipà  (pronounced or ; Latrodectus katipo) is a species of cobweb spider found only in New Zealand. It is one of many species in the genus Latrodectus and is most closely related to the Australian redback (L. hasseltii). It is venomous to humans, its bite being capable of producing the toxic syndrome latrodectism; symptoms include extreme pain and, potentially, hypertension or seizure. Bites are rare and antivenom is available in some hospitals. The female is in length; the male is . In the South Island and the lower half of the North Island the female has a distinct red stripe bordered in white on its abdomen; in more northern populations this stripe is absent, pale, yellow, or replaced with cream-coloured blotches. These two forms were previously thought to be separate species. The male is white with black stripes and red hourglass-shaped markings.
The katipà  is mainly found living in sand dunes close to the seashore. It is found throughout most of coastal New Zealand except the far south and the West Coast. It feeds mainly on ground-dwelling insects, caught in an irregular tangled web spun among dune plants or other debris. After mating, the female katipà  produces five or six egg sacs in November or December. The juveniles hatch after 20âÂÂ25 days and during January and February they disperse into surrounding plants. The common name is from MÃÂori for "night stinger", which is derived from the words (to sting) and (the night). Due to habitat loss, colonisation of their natural habitat by invasive spiders and hybridisation with L. hasseltii, the katipà  is listed as "in serious decline" by the New Zealand Threat Classification System.
The katipà  was reported as early as 1855 as the kÃÂtÃÂpo, but was not formally described in taxonomic literature until 1870 when New Zealand doctor Llewellyn Powell described it as Latrodectus katipo. Swedish arachnologist Tamerlan Thorell later placed it in Latrodectus scelio, a previous name for Latrodectus hasseltii (redback spider). Later, New Zealand arachnologist Arthur Urquhart unknowingly described it again as two species: Theridium melanozantha in 1887 and Theridium zebrinia in 1890. He also described Latrodectus katipo var. atritus, a subspecies of katipà  that was fully black in colour. In 1933 Urquhart's two species were later recognised to be the same as L. katipo by American arachnologist Elizabeth Bryant and thus were synonymised. Several taxonomic studies have disagreed over whether to treat L. katipo as a separate species or as a synonym of L. hasseltii with L. atritus as a subspecies. Eventually, it was concluded that L. katipo, together with L. katipo var. atritus, are separate from L. hasseltii.
There was further confusion over whether L. katipo and L. katipo var. atritus should be considered separate species due to their very similar morphology but notably different distributions. Although they were designated as separate species for a time, this was clarified when the species was revised again in 2008. In this revision, L. atritus was formally recognised to be the same as L. katipo on the basis of genetic data and thus was synonymised. It was proposed that the colour variation seen between these two groups is a cline, or gradual continuous variation over latitude and is correlated with mean annual temperature.
The katipà  is a member of the genus Latrodectus. This genus has a worldwide distribution with notable members such as Latrodectus mactans (black widow spider), Latrodectus geometricus (brown widow spider) and Latrodectus hasseltii (redback spider), the latter of which the katipà  is most closely related to. It is a member of the family Theridiidae, which are commonly known as cobweb spiders or comb-footed spiders.
The common name and specific name katipà  (singular and plural), often spelt "katipo", is MÃÂori for "night stinger", derived from the words kakati (to sting) and pà  (the night). It is one of the few MÃÂori words that refers to a specific species of spider. The fully black variant is referred to as black katipà Â.
A 2004 study examined the genetic relationships of Latrodectus spiders using sequences from part of the cytochrome c oxidase subunit I gene. The study found that the katipà  are most closely related to the Australian Latrodectus hasseltii (redback spider). The katipà  are so closely related to the redback that the katipà  was thought to be a subspecies of the redback. Further research has shown that the katipà  is genetically and morphologically distinct from the redback, having slight structural differences and striking differences in habitat preference.'
As an adult, the female has a body size of or if leg span is included. The red katipà Â, found in the South Island and the lower North Island, has a large black globular abdomen with a silky appearance and a distinctive white-bordered orange or red stripe on its upper surface that runs from the beginning of the abdomen back to the spinnerets. The underside of the abdomen is black and has a red patch or partial red hourglass-shaped marking. For the black katipà Â, found in the upper North Island, the abdomen differs in not having the upper red/orange stripe and is overall somewhat lighter in colour. The hourglass pattern on the underside of the abdomen may also be less distinct, losing the middle section. Rare variations in black katipà  also exist where the abdomen, cephalothorax, or entire body is brown, sometimes with a dull red or yellow stripe, or cream-coloured spots on its upper side.
The katipà  is most similar to its sister species Latrodectus hasselti. The katipà  can be distinguished from L. hasselti by the short setae (hair-like spines) of the abdomen, whereas on the abdomen of L. hasselti it is a mix of long and short setae. There are also minor differences in the shape of the female and male genitalia structures. It may also be confused for Steatoda species, which are often present in the same habitat. One of the species, Steatoda capensis is so similar that they are commonly referred to in New Zealand as "false katipà Â". The katipà  has a less shiny and more tapered abdomen and the lateral eyes (eyes at the side of the head) are further apart.
As juveniles, the female and male are identical until their fourth instar, a developmental stage that occurs between moults. Before this, they are coloured whitish and have black markings running vertically down the abdomen. The abdomen also frequently has traces of red. The male, which is in length, keeps this juvenile colour pattern as an adult.
The katipà  is only found in New Zealand. In the North Island it is found throughout the West Coast from North Cape to Wellington. On the east coast of the North Island it occurs irregularly, but it is abundant on Great Barrier Island. In the South Island it is found in coastal regions south to Dunedin on the east coast and south to Greymouth on the west coast. It has been proposed that this southern limit is due to the katipà  needing warmer temperatures to allow for the development of their eggs.
The red katipà  is found south of the western tip of Taranaki on the west coast, and just north of Waipatiki Beach in Hawke's Bay on the east coast. The black katipà  are found north of Aotea Harbour in the Waikato region on the west coast, and Waipiro Bay in the Gisbourne region on the east coast. Both forms are found in a transitionary area in between these aforementioned localities. These colour variants are strongly correlated with temperature, one study reporting that the red katipà  is found in cooler areas with average temperatures of 11.24âÂÂ13.85ðC. In contrast, the black katipà  is found in warmer areas with average temperatures of 13.64âÂÂ16.23ðC.
The katipà  is restricted to coastal sand dunes near the seashore. It generally resides on the landward side of dunes closest to the coast where it is most sheltered from storms and sand movement. It can sometimes be associated with dunes several kilometers from the sea when these dunes extend inland for long distances.Webs are typically established in low-growing dune plants and other vegetation such as the native pëngao (Ficinia spiralis) or the introduced marram grass (Ammophila arenaria). It may also build its web under driftwood, stones, or other debris such as rubbish. This behaviour can be exploited by researchers and conservationists by placing plywood lids in katipà  habitat, which the spider hides under and can thereby have its populations easily sampled. Webs are almost always constructed over open sand and near the ground so as to catch crawling insects for food. The katipà  inhabiting dune grasses constructs its web in open spaces between the grass tufts; the katipà  inhabiting areas of shrubbery does so on the underside of a plant overhanging open sand. It has been found that these patches of open sand are necessary for the katipà  to build its web as plants that envelop sand dunes in dense cover, such as invasive plants like kikuyu or buffalo grass, create an environment unsuitable for web construction. The katipà  commonly spins its web among pëngao as this plant's growth pattern leaves patches of sand between each plant. Marram grass has been extensively planted in New Zealand to help stabilise sand dunes and has largely replaced pëngao in many areas. Because marram grass grows in a very tight formation only leaving small gaps between tuffs, this makes it difficult for the katipà  to construct a suitable web for capturing prey. Due to this, it has been demonstrated that the katipà  is less abundant in dunes dominated by marram grass than they are in dunes dominated by pëngao.
Once it becomes an adult, the male begins to search for a female to mate with, possibly being guided by pheromones in female's silk. The male enters the female's web and gently vibrates the silk as he approaches her. The female is usually aggressive at first and will chase the male from the web. The courtship process consists of the male bobbing, plucking and tweaking the web along with periods of cautious approach and being chased by the female. Eventually, when she becomes docile and allows him to approach. The male moves to the underside of her abdomen, tapping her rapidly until their abdomens are aligned in the same direction. He then inserts his palps (appendages modified for reproduction) into the female's reproductive tract one at a time. Copulation occurs over 10 to 30 minutes. After mating, the male retreats to groom, which is performed by running his palps and legs through his fangs and wiping them over his body. The male is not eaten by the female unlike some other widow spiders.
The female lays its eggs in November or December. The eggs are round, about the size of a mustard seed, and are a transparent, purplish red. They are held together in a cream-coloured, round, ball shaped egg sac which is about in diameter. The female constructs five or six egg sacs over the next three to four weeks. Each egg sac contains about 70 to 90 fertilised eggs. The egg sacs are hung in the centre of the spider's web and the female spins more silk over them, which becomes covered in sand and conceals them somewhat.
The eggs hatch after 20âÂÂ25 days and continue to develop within the egg sac where they remain until the second instar, at which stage they feed on the wall of the egg sac. After four to six weeks of incubation, during January and February, the juveniles chew their way out of the egg sac. The young spiders then disperse from the web. In one 24-hour study of juveniles, 28% dispersed from the web by ballooningâÂÂusing air currents to carry themselves away from the nest on a single silk strand. The majority, 61%, used bridging, moving to nearby plants along silk threads, while 11% remained in the nest.
Because they are closely related, the male redback is able to successfully interbreed with a female katipà  to produce hybrid offspring. However, a male katipà  cannot mate with the female redback as the male katipà  is heavier than the male redback, and when it approaches the web it triggers a predatory response in the female leading to the male usually being eaten before mating can occur. There is evidence of interbreeding between katipà  and redbacks in the wild, one specimen reported to have redback DNA in its maternal lineage.
The proportion of females, males and juveniles in a population varies somewhat depending on site. As adults, the female is generally more abundant than the male, probably because the male lives on average 77 days whereas the female can live for two years. Along the Manawatu-Whanganui coastline, only adult females were found in some surveyed sites whereas at other sites the juveniles were more common than the adults. It has been proposed that sites with few juveniles detected may be due to low reproductive output.
Katipà  prey varies depending upon location, but it typically catches wandering ground invertebrates such as beetles (e.g. Cecyropa modesta) or amphipods (e.g. Bellorchestia quoyana), but it may occasionally catch moths, flies, and other spiders. The katipà  can catch insects much larger than it. These insects often become entangled in the web and in the ensuing struggle, the web's ground anchor line breaks. The silk's elasticity causes smaller prey to become suspended a few centimetres off the ground. Whether the prey is suspended, and how high, depends on how heavy the prey is. Earwigs caught in the web are not suspended at all whereas slaters, which are much lighter, can be suspended at varying heights. The katipà  then moves to the prey, turns so that the spinnerets are facing it and spins silk over it. Like most theridiids, the tarsi (last leg segment) of the hind legs have a row of strong curved bristles which are arranged as a comb. The katipà  uses these to scoop sticky silk from its spinnerets and throws it over the insect with a series of rapid movements. After the insect is firmly immobilised, the spider bites it several times, usually at the joints, before spinning more silk to strengthen the web, and then administering a last long bite which ultimately kills the insect. The spider then moves the prey up into the web until it is ready to eat. If food is readily available then it is common to see five or six insects hanging in the web waiting to be ingested. The male's hunting behaviour is similar to the female's, although may not be as powerful due to its smaller size.
Like other theridiid spiders, the web is a seemingly disorganised tangle of silk. The structure consists of a retreat for the katipà  to hide in and a catching web for obtaining prey. The retreat is loosely tube shaped with an open end and is generally formed inside the base of coastal tussocks or other debris. The walls of the retreat are interwoven and waterproof. The catching web extends out from the retreat and can be divided into three layers. The upper and middle layers are constructed horizontally. Of these, the upper layer is formed as a network of mesh that supports the middle layer, which forms a dense latticed sheet that extends in all directions. The lower layer is constructed vertically, with threads extending from the above layers to the ground. These threads have viscous droplets that can assist in capturing prey. The web is spun during the early morning and at night. If the web is destroyed it can be rebuilt overnight rather quickly.
The eggs of the katipà  have been observed being eaten by a small, undescribed native wasp from the family Ichneumonidae. It has also been proposed that house mice, which are not native to New Zealand, prey upon the katipà Â.
Under the New Zealand Threat Classification System, the katipà  is listed as "Declining", with the qualifiers of "Climate Impact", "Data Poor: Trend" and "Range Restricted". Several factors have contributed to its decline; the major ones appear to be habitat loss and the declining quality of the remaining habitat. Human interference with their natural habitat has been occurring for over a century following European settlement. Coastal dune modification resulting from agriculture, forestry, or urban development, along with recreational activities like the use of beach buggies, off-road vehicles, beach horse riding and driftwood collection have destroyed or changed areas where the katipà  lives. The introduction of many invasive invasive plants may have also contributed to the decline of suitable habitat. It has also been proposed that surfactants, which are used to improve herbicide efficiency, may pose a risk to the katipà Â.
Much of the katipà  habitat is also occupied by the invasive spider Steatoda capensis (commonly known as "false katipà Â" in New Zealand), a South African species that became common in New Zealand during the 20th century. Both species can be found sharing the same dune systems or even co-existing under the same piece of driftwood. There is evidence that displacement of the katipà  is occurring due to the ability of S. capensis to quickly recolonise areas from which the katipà  had been displaced after storms or other dune modifications. Furthermore, S. capensis breeds year-round, produces more offspring and lives in a greater range of habitats which leads to greater pressure on the katipà Â.
In 2010 the katipà  was one of a dozen species of previously unprotected invertebrate given full protection under the 1953 Wildlife Act, noted as "iconic, vulnerable to harm, and in serious decline". Under the Act, killing an absolutely-protected species such as the katipà  is punishable by a fine or even imprisonment. It has been proposed that restoration of sand dune habitat, including the replacing of marram grass (Ammophila arenaria) with native dune plants, would provide more suitable habitat for the katipà  to conserve their populations. Reducing activities that damage sand dunes, such as off-road driving and rubbish dumping may also protect the species.
The katipà  has venom that is medically significant in humans, meaning it has the potential to cause serious injury or death. Antivenom is available in some hospitals to treat bites. No deaths due to the bite have been recorded in medical settings. The incidence of bites is low as it is a shy, non-aggressive spider. Their narrow range, diminishing population, and human awareness of where they live means humans rarely encounter katipà Â. The katipà  will only bite defensively. If the female is with an egg sac it will remain close by it and be more aggressive. Envenomation from bites of the katipà  cause effects known as latrodectism. The venoms of all Latrodectus spiders are thought to contain similar components with the neurotoxin ñ-latrotoxin being the main agent responsible. One study reported that only the female is capable of biting humans.
MÃÂori legends recall deaths due to bites. One legend states that an entire group of MÃÂori camped out at the mouth of the Whanganui River were bitten overnight, and two died. In MÃÂori tradition, katipà  bite victims would be treated by bathing them in hot water or covering the bite wound in red ochre, which supposedly reduced swelling and pain. Alternatively they would also cover the victim in smoke. Bites are very rare, 23 of the 37 known hospitalisations for spider bites between 1967 and 1976 in New Zealand being attributed to katipà  bites. The most recent reported katipà  bites () were to a Canadian tourist in 2010 and a kayaker in 2012, both of which survived.
The symptoms of a katipà  bite are considered to be extremely similar to the bite of L. hasselti. Initially, the bite may be painful, but sometimes only feels like a pin prick or mild burning sensation. Within an hour victims generally develop more severe local pain with local sweating and sometimes piloerection (goosebumps). Pain, swelling and redness spread away from the site. Less commonly, systemic envenoming is heralded by swollen or tender regional lymph nodes; associated features include malaise, nausea, vomiting, abdominal or chest pain, generalised sweating, headache, fever and hypertension. The duration of effects can range from a few hours to days, with severe pain persisting for over 24 hours after being bitten in some cases.
Treatment is based on the severity of the bite; only oral analgesics being needed in less severe cases or parenteral analgesics being used in more severe cases. If symptoms do not resolve, then redback antivenom may be used, which can neutralise the katipà  venom. Stocks of the antivenom are available in some New Zealand hospitals. Unlike some other antivenoms, it is not limited to patients with signs of severe, systemic envenoming. Opioids and benzodiazepines can be used as an initial treatment for latrodectism.