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Biology

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According to the IUCN/SSC Invasive Species Specialist Group A. gracilipes is among the 100 most pervasive and destructive invasive species in the world (Lowe, et al., 2000), and is most notably implicated in the 'ecological meltdown' of Christmas Island (O'Dowd, et al., 2001;2003). Introduced populations of Anoplolepis gracilipes can exhibit unicolonial behavior by forming multiple, populous high-density supercolonies. On Christmas Island, A. gracilipes was recorded to achieve the highest density of foraging ants ever recorded (Abbott, 2005). Colonies are polydomous and polygynous and disperse by budding. Nests occasionally hosting hundreds of queens and thousands of workers. The species has generalized foraging and nesting habits, and often achieve high densities in agricultural landscapes. Part of the species invasion success has been attributed to its strong mutualisms with nectar and honeydew producing insects like scales and aphids.

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Distribution Notes

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Global (Wetterer 2005): In tropical Asia and tropical islands of the Indian and Pacific Oceans, A. gracilipes occurs throughout the moist lowlands, but is not commonly found in arid regions and sites above 1200 m elevation. In tropical Africa, it is known only from Dar es Salaam and nearby Zanzibar. In tropical Australia, A. gracilipes has been recorded primarily from moist monsoon rainforests along perennial springs and streams in the northern region and in a few towns on the north and east coasts. In the Neotropics, there are records of A. gracilipes from western Mexico. In subtropical Asia, A. gracilipes ranges up to 26-27N in northern India, southern China, and southern islands of Japan. I found only six records from latitudes >27, two from exterminated urban populations (Auckland, New Zealand; Brisbane, Australia) and three from probably temporary populations (Valparaso, Chile; Durban, South Africa; Zayul, Tibet). The sixth population, on Amami-Oshima Island, Japan, may or may not be temporary. Anoplolepis gracilipes is not yet known from many moist lowland tropical areas where it would probably thrive, including west-central Africa and much of the Neotropics. Populations in western Mexico are prevented from expanding eastward by a central mountain range, but may be able to spread south, around the mountains, to the Caribbean, Central America, and South America. Records from arid Baja California, Mexico indicate that A. gracilipes can invade and persist in areas with arid climates, perhaps due to moderating effects of irrigation.Fiji (Sarnat & Economo, in prep): Viti Levu, Vanua Levu, Taveuni, Kadavu, Gau, Koro, Moala, Lakeba, Beqa, Yasawa Is., Macuata Is., Nanui-i-Ra I.Hawaii: Kauai, Oahu, Maui and Hawaii
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Identification

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Anoplolepis gracilipes is a large, slender, brownish yellow species most easily identified by it extraordinarily long limbs. The antennal scapes are greater than 1.5x the head length, and the full antennae are longer than the entire body from the apical tip of the mandibles to the distal tip of the gaster. The head is ovoid and distinctly longer than broad. The antennae are 11-segmented and the mandibles have 8 teeth. The eyes are large and bulge well beyond the outline of the head in full face view. The mesosoma is long and slender. The pronotum in particular, is extended anteriorly giving the appearance of a long 'neck'. The mesonotal dorsum slopes downward towards the propodeum. The propodeum is gently rounded and convex, with approximately equal posterior and dorsal faces. The petiolar node is thick and upright with a longer posterior face than anterior face. The gaster is armed with an acidopore and tends to be darker than the rest of the body.

Among introduced ants, Anoplolepis gracilipes might be mistaken for Paratrechina longicornis (the Black Crazy Ant), which also has very long antennae and legs and eyes that break the outline of the head in full face view. In addition to the difference in color, A. gracilipes can also be distinguished by the lack of erect hairs on the mesosoma, petiole and gaster. Anoplolepis gracilipes can also be mistaken for species of Leptomyrmex and Oecophylla because of their similar sizes and very long limbs. Anoplolepis can be distinguished from Leptomyrmex by the presence of an acidopore. Anoplolepis can be distinguished from Oecophylla by the more compact petiole.Diagnosis among introduced and commonly intercepted ants.Antenna 11-segmented. Antennal club indistinct. Antennal scape length greater than 1.5x head length. Eyes large; break outline of head. Antennal sockets and posterior clypeal margin separated by a distance equal to or greater than the minimum width of antennal  scape. Dorsum of mesosoma with metanotal impression, but never with a deep and broad concavity. Metapleuron with a distinct gland orifice. Propodeum and petiolar node both lacking a pair of short teeth. Propodeum lacking posteriorly projecting protrusion. Propodeal declivity less than twice length of propodeal dorsum. Waist 1-segmented. Petiole upright and not appearing flattened. Gaster armed with acidopore. Distinct constriction not visible between abdominal segments 3+4. Hairs not long thick and produced in pairs. Yellowish-brown to reddish-brown. Monomorphic.

Male identification among New World Formicinae Antenna 12-merous; mandible with 8-9 denticles, with one or two offset denticles on basal margin; maxillary palps longer than maximum compound eye length; scape more than twice head length; compound eyes situated at about head midlength.

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Taxonomic History

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Formica gracilipes Smith, 1857a PDF: 55 (w.) SINGAPORE. Indomalaya. AntCat AntWiki HOL

Taxonomic history

Replacement name for Anoplolepis longipes (Jerdon, 1851). [Junior primary homonym of Pheidole longipes (Latreille, 1802).].[Note: Anoplolepis gracilipes (Smith, 1857) junior synonym of Anoplolepis longipes (Jerdon, 1851) (synonymy by Emery, 1887a PDF: 247, etc.); hence Anoplolepis gracilipes (Smith, 1857) first available replacement name for Anoplolepis longipes (Jerdon, 1851) (Bolton, 1995b: 67).].Mayr, 1867a PDF: 73 (q.).Combination in Prenolepis: Mayr, 1862 PDF: 698.Combination in Plagiolepis: Mayr, 1867a PDF: 73.Combination in Anoplolepis: Bolton, 1995b: 67.Junior synonym of Anoplolepis longipes (Jerdon, 1851): Emery, 1887a PDF: 247; Dalla Torre, 1893 PDF: 173; Pergande, 1894 PDF: 163; Forel, 1894c PDF: 415; Mayr, 1895 PDF: 149; Forel, 1899b PDF: 124; Wheeler, 1919f PDF: 101; Wheeler, 1922: 933; Emery, 1925d PDF: 17; Donisthorpe, 1932c PDF: 444; Baltazar, 1966 PDF: 266; Kempf, 1970b PDF: 30; Kempf, 1972b PDF: 22; Snelling & Hunt, 1975 PDF: 114.Status as species: Smith, 1858a PDF: 22; Smith, 1859a PDF: 136; Smith, 1860a PDF: 68; Mayr, 1862 PDF: 698; Roger, 1863b PDF: 10; Mayr, 1863a PDF: 451; Mayr, 1865 PDF: 50; Mayr, 1867a PDF: 73 (redescription); Smith, 1871a PDF: 305; Mayr, 1872 PDF: 144; Mayr, 1876 PDF: 78; Emery, 1883 PDF: 147; Rothney, 1889 PDF: 373; Mayr, 1893b PDF: 197; Bolton, 1995b: 67; Zhou, 2001a PDF: 174; Wetterer, 2002 PDF: 129; Blard et al., 2003 PDF: 129; Bolton, 2003 PDF: 267; Imai et al., 2003 PDF: 82; Wetterer & Vargo, 2003 PDF: 417; Jaitrong & Nabhitabhata, 2005 PDF: 13; Wetterer, 2005 PDF: 77; Wetterer, 2006 PDF: 415; Don, 2007: 201; Clouse, 2007b PDF: 223; Framenau & Thomas, 2008 PDF: 61; Terayama, 2009 PDF: 206; Mohanraj et al., 2010 PDF: 6; Collingwood et al., 2011 PDF: 448; Pfeiffer et al., 2011 PDF: 36; Ran & Zhou, 2011: 66; Borowiec & Salata, 2012 PDF: 463; Guénard & Dunn, 2012 PDF: 27; Sarnat & Economo, 2012 PDF: 43; Sarnat et al., 2013 PDF: 69; Borowiec, 2014 PDF: 8; Ramage, 2014 PDF: 56; Bharti et al., 2016 PDF: 23; Jaitrong et al., 2016 PDF: 26.Senior synonym of Anoplolepis trifasciata: Mayr, 1867a PDF: 73; Mayr, 1872 PDF: 144; Dalla Torre, 1893 PDF: 173; Bolton, 1995b: 67; Zhou, 2001a PDF: 174.
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Brief Summary

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The yellow crazy ant Anoplolepis gracilipes, also known as the long-legged ant or the Maldive ant, is one of the five species of “tramp ant” species, known for invasive behavior and devastating ecological effects. The Invasive Species Specialist Group (ISSG) considers it among the top 100 of the world’s worst invaders. Its native origin is not certain, but thought to be either in West Africa or Asia; it has been introduced across the world’s tropical and sub-tropical areas, including many Pacific Islands, Northern Australia, the Carribean, and some Indian Ocean islands. Perhaps its most notorious devastation is on Christmas Island, where it caused an “Invasional meltdown” (O’Dowd et al 2003), decimating red land crab (Gecarcoidea natalis) populations, a keystone species whose demise has significantly altered the islands ecology and negatively effected endemic species. There is grave concern about spread of A. gracilipes in northern and north-eastern Australia, where a huge eradication campaign is underway. Several features of the yellow crazy ant contribute to its destructive ecological impacts: • It has a generalist diet and is a competitive forager, making huge colonies (in some cases “supercolonies” containing multiple queens) with enormous nutritional needs. It preys on or interferes with the survival of a large variety of rainforest arthropods, reptiles, birds and mammals. • It forms tight mutualisms with sap-sucking scale insects, boosting scale populations and consequentially boosting sooty mold growth, both which negatively impact rainforest health. • It colonizes agricultural areas making it easily carried to new regions by humans in boats, road vehicles, and farm equipment. • It has a very rapid colony spread rate, in one instance on Christmas Island colony expansion was measured at 3 m/day. The yellow crazy ant is so called for its erratic, fast movements, especially when disturbed. For an invasive ant, this ant is large in size. It is yellow-orange in color and has long legs and antennae. (O'Dowd 2003, 2009; PiaKey; Wikipedia 2011)
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Yellow crazy ant

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The yellow crazy ant (Anoplolepis gracilipes), also known as the long-legged ant or Maldive ant, is a species of ant, thought to be native to West Africa or Asia. They have been accidentally introduced to numerous places in the world's tropics.[2][3]

The yellow crazy ant has colloquially been given the modifier "crazy" on account of the ant's erratic movements when disturbed. Its long legs and antennae make it one of the largest invasive ant species in the world.[1][4]

Like several other invasive ants, such as the red imported fire ant (Solenopsis invicta), the big-headed ant (Pheidole megacephala), the little fire ant (Wasmannia auropunctata), and the Argentine ant (Linepithema humile), the yellow crazy ant is a "tramp ant", a species that easily becomes established and dominant in new habitat due to traits such as aggression toward other ant species, little aggression toward members of its own species, efficient recruitment, and large colony size.[5]

It is on a list of "one hundred of the world's worst invasive species" formulated by the International Union for Conservation of Nature (IUCN),[6] having invaded ecosystems from Hawaii to the Seychelles, and formed supercolonies on Christmas Island in the Indian Ocean.[7]

In 2023, a scientific article postulated a unique reproductive cycle for A. gracilipes, suggesting that males are obligate chimeras.[8]

Physiology

Anoplolepis gracilipes is a relatively large, yellow to orange ant with long legs, large eyes and extremely long antennal scapes.

Although A. gracilipes is the only invasive species in the genus Anoplolepis, there are several other genera for which it can be mistaken. Both Leptomyrmex and Oecophylla can be confused with Anoplolepis because of their similar sizes and very long limbs. Anoplolepis can be distinguished from Leptomyrmex by the presence of an acidopore, while Anoplolepis can be distinguished from Oecophylla by the more compact petiole. Although both of these genera occur in the Pacific, neither contain any invasive species.

Several species of invasive ants belonging to the genera Camponotus and Paratrechina can appear similar to A. gracilipes. Although several invasive species of Pheidole can also be slender-bodied with long legs and long antennal scapes, they can be separated from A. gracilipes by their two-segmented waists.

A. gracilipes is widespread across the tropics, and populations are especially dense in the Pacific region. The species is most infamous for causing the ecological "meltdown" of Christmas Island.[9][7] Although widespread across the Pacific, A. gracilipes can cause significant damage to native biological diversity. Strong quarantine measures are encouraged to keep it from spreading to new localities.

Geographical range and dispersal

A dead gecko being dragged by yellow crazy ants in India

The yellow crazy ant's natural habitats are the moist tropical lowlands of Southeast Asia, and surrounding areas and islands in the Indian and Pacific Oceans.[10] It has been introduced into a wide range of tropical and subtropical environments including northern Australia, some of the Caribbean islands, some Indian Ocean islands (Seychelles, Madagascar, Mauritius, Réunion, the Cocos Islands and the Christmas Islands)[7] and some Pacific islands (New Caledonia, Hawaii, French Polynesia, Okinawa, Vanuatu, Micronesia, Johnston Atoll, and the Galapagos archipelago).[11][12] The species has been known to occupy such agricultural systems as cinnamon, citrus, coffee and coconut plantations. Because yellow crazy ants have generalized nesting habits, they are able to disperse via trucks, boats and other forms of human transport.[1]

Crazy ant colonies naturally disperse through "budding", i.e. when mated queens and workers leave the nest to establish a new one, and only rarely through flight via female winged reproductive forms. Generally, colonies that disperse through budding have a lower rate of dispersal, requiring human intervention to reach distant areas. It has been recorded that A. gracilipes moves as much as 400 m (1,300 ft) a year in the Seychelles.[11] A survey on Christmas Island, however, yielded an average spreading speed of 3 meters (9.8 ft) per day, the equivalent of one kilometer (0.6 mile) per year.[13]

Diet

A. gracilipes (yellow crazy ants) moving dead Blattidae sp. (cockroach) toward their nest in Pohnpei, Federated States of Micronesia

A. gracilipes has been described as a "scavenging predator" exhibiting a broad diet, a characteristic of many invasive species. It consumes a wide variety of foods, including grains, seeds, arthropods, and decaying matter such as vertebrate corpses. They have been reported to attack and dismember invertebrates such as small isopods, myriapods, molluscs, arachnids, land crabs, earthworms and insects.[13]

Like all ants, A. gracilipes requires a protein-rich food source for the queen to lay eggs and carbohydrates as energy for the workers. They get their carbohydrates from plant nectar and honeydew producing insects, especially scale insects, aphids, and other Sternorrhyncha. Studies indicate that crazy ants rely so much on scale insects that a scarcity of them can actually limit ant population growth.[11]

Reproduction

Similar to other ants, the queen produces eggs which are fertilized by male sperm that are stored in sperm stores. When an egg is fertilized, there are three distinct events that can happen: (i) the resulting diploid organism develops into a queen if the egg is fertilized by an R sperm or (ii) into an infertile diploid worker if the egg is fertilized by a W sperm. However, a third outcome has been described in a 2023 scientific study: (iii) the egg is fertilized by a W sperm but the parental nuclei bypasses the fusion of the two gametes and divide separately within the same egg, leading to a haploid male that is chimeric with a portion of cells carrying the W genome and a portion of cells carrying the R genome.[8] Interestingly, not all tissues have equal proportions of each cell line, with sperm cells mostly carrying the W genome and thus providing the W alleles with a fitness advantage.[8] This is the first known case of obligate chimerism in animals.[14][15]

Mutualism

Crazy ants obtain much of their food requirements from scale insects, serious plant pests that feed on sap of trees and release honeydew, a sugary liquid. Ants eat honeydew, and in return protect the scale from their enemies and spread them among trees, an example of mutualism. The honeydew not eaten by the ants drips onto the trees and encourages the growth of sooty mold over the leaves and stems. This gives plants an ugly black appearance and reduces their health and vigor.

The ants protect the insects by "nannying" the mobile crawler stages and protecting them against their natural enemies.[16] Experiments have shown that this connection is so strong that, in environments where A. gracilipes was removed, the density of scale insects dropped by 67% within 11 weeks, and to zero after 12 months.[17]

In Australia

In Australia, yellow crazy ants have been found at more than 30 sites in Queensland, and in Arnhem Land in the Northern Territory, where a large scattered population exists.[18] A single New South Wales infestation was detected and eradicated, and, in Western Australia, yellow crazy ants have been intercepted in shipping freight arriving at Fremantle.[19]

Queensland's main infestation is 830 hectares (2,100 acres) in and around Wet Tropics of Queensland rainforest, a World Heritage Site.[18] The Northern Territory infestation covers 2,500 square kilometres (970 sq mi),[19] an area larger than the Australian Capital Territory.[20]

Climate modelling indicates yellow crazy ants could spread across northern Australia from Queensland to Western Australia, across much of Queensland and into coastal and inland parts of New South Wales.[19] Areas with the most ideal habitat and climatic conditions, such as the Wet Tropics of Queensland rainforests, are likely to experience the highest impacts.[21]

A cost–benefit analysis by the Queensland government undertaken in 2012 found that yellow crazy ants could cost Australia's economy over A$3 billion if the ants were not treated. This analysis did not take potential impacts on Australia's biodiversity into account.[21] The known impacts of crazy ants in tropical rainforests overseas may provide useful insights into these impacts, bearing in mind that the most significant impacts are associated with relatively small islands, such as Christmas Island.[19][7]

Impact on Christmas Island

Crazy ants have had a profound impact on the biodiversity of Christmas Island.[19][7]

The crazy ant has a significant destructive impact on the island's ecosystem, killing and displacing crabs on the forest floor. The supercolonies also devastate crab numbers migrating to the coast. This has seen a rapid depletion in the number of land crabs[7] — killing up to 20 million of them[7] — which are vital to Christmas Island's biodiversity; land crabs are a keystone species in the forest ecology: they dig burrows, turn over the soil, and fertilize it with their droppings.[22]

Seedlings that were previously eaten by crabs started to grow and, as a result, changed the structure of the forest. Weeds have spread into the rainforest because there are no crabs to control them. One of the most noticeable changes in the forest is the increased numbers of the stinging tree Dendrocnide peltata, which now flourishes in many areas frequently visited by humans. The forest canopy also changed as the scale insects tended by yellow crazy ants multiplied and killed mature trees.[23][21]

Christmas Island red crabs are completely wiped out in infested areas.[7] Populations of other ground and canopy dwelling animals, such as reptiles and other leaf litter fauna, have also decreased. During crab migrations, many crabs move through areas infested with ants and are killed. Studies show that the ant has displaced an estimated 15–20 million[7] crabs by occupying their burrows, killing and eating resident crabs, and using their burrows as nest sites. This factor has greatly depleted red crabs, and made their annual land migrations far more perilous.[24][25]

Although crazy ants do not bite or sting, they spray formic acid as a defence mechanism and to subdue their prey. In areas of high ant density, the movement of a land crab disturbs the ants and, as a result, the ants instinctively spray formic acid as a form of defence. The high levels of formic acid at ground level eventually overwhelm the crabs, and they are usually blinded then eventually die from dehydration (while attempting to flush off the formic acid) and exhaustion. As the dead crabs decay, the protein becomes available to the ants.[21]

Crazy ants kill fauna, but encourage scale insects. Increased densities of scale insects cause forest die back, and even the death of large forest trees. These changes create a cascade of negative impacts, including weed invasion, significantly altering the forest landscape.

Supercolonies

Christmas Island is a focal point for international control efforts. These supercolonies spread farther and cause more damage than single colonies, and they pose the single greatest known threat to the island's biodiversity.

Staff from Christmas Island National Park have worked in recent years to keep ant numbers in check. With help from the Christmas Island Crazy Ant Scientific Advisory Panel and support from the Australian Government they are holding ground.

Another supercolony nearly devastated the bird fauna of Johnston Atoll in the Pacific Ocean. The single massive colony was found to occupy nearly a quarter of the island, with up to 1,000 queens in a plot of land 6 metres (20 ft) wide. The infestation is thought to have been eradicated.[26]

Control measures

To reduce the impacts of crazy ants on red crabs and Christmas Island's ecosystems the Parks Australia carried out a major aerial baiting program in 2009, to follow up the first aerial baiting conducted in 2002. The first step was conducting an extensive island-wide survey to determine the exact locations of the supercolonies. For several months, staff traversed the island surveying over 900 sites. The result was a map of crazy ant supercolonies and red crab burrow densities, together with other biodiversity data.

In September 2009, a helicopter was used to precisely bait crazy ant supercolonies, which covered 784 hectares (1,940 acres) of the island. A very low concentration of fipronil bait (0.1%) was used to control the ants. Monthly monitoring of these baited supercolony sites shows that crazy ant densities were reduced by 99%.

Park staff placed a high emphasis on minimising non-target impact of baiting. Food lures were dropped from a helicopter to attract robber crabs away from areas that were about to be baited. This technique, combined with the low concentration fipronil bait, proved to be highly successful with extremely low numbers of robber crabs and no red crabs known to be killed by the baiting.

While baiting has slowed the decline of the red crab, its effects on the crazy ant populations are only temporary, as escaping colonies invade the treated areas again, and it is expensive, requiring much man power. In an effort to find a better control, after research, Australian Parks in December 2016 imported Tachardiaephagus somervillei, a small (2 millimetres (564 in)) wasp and began breeding them for release. The wasp, which attacks only scale insects, is a voracious predator of what is believed to be one of the crazy ant's largest source of honeydew on Christmas Island, the yellow lac scale insect.[27]

Researchers from La Trobe University in Melbourne, funded by Parks Australia, began looking for biological controls in 2009. While the ants are omnivores, studies have shown honeydew is an important part of the diet of Christmas Island crazy ants. Samples of ants taken from colonies that are growing rapidly have more honeydew in their diet than when the colonies decline. Further, restricting access to honeydew, by binding trees where the scale insects feed, dramatically reduced the colony as ant activity on the ground fell by 95% in just four weeks.[28] In the laboratory, colonies with limited sources of sugar were compared to colonies with access to abundant sugar. Those with abundant sugar had more fertile queens and lower death rates among workers. The workers were also more aggressive toward other ant species and explored their environments more. This is believed to show why the ants decline when deprived of access to scale insects in the field, and confirm reduced honeydew will greatly reduce the ants' ability to form super colonies.[24]

While controlling the scale insect is expected to control the yellow crazy ant on Christmas Island, on mainland Australia it is thought this would not help. There are at least a dozen honeydew producing insects as well as extrafloral nectar from native acacia trees, all of which fuel yellow crazy ants.[27]

Experts continue to call for a fully funded, long term baiting program on mainland Australia.[29]

References

  1. ^ a b c Anoplolepis gracilipes. Global Invasive Species Database. ISSG.
  2. ^ Davies, Ella. "Battle of the Ants". BBC. BBC. Retrieved 2021-08-05.
  3. ^ "One Remote Island's Battle Against Acid-Spewing Ants". Audubon. 2015-06-26. Retrieved 2022-04-02.
  4. ^ "Pests and Diseases Image Library: Anoplolepis gracilipes". Archived from the original on 2008-07-29.
  5. ^ Kirschenbaum, R. and Grace, J. K. 2008. "Agonistic responses of the tramp ants Anoplolepis gracilipes, Pheidole megacephala, Linepithema humile, and Wasmannia auropunctata (Hymenoptera: Formicidae)" (PDF). Sociobiology. 51 (3): 673–84.{{cite journal}}: CS1 maint: multiple names: authors list (link)
  6. ^ One Hundred of the World's Worst Invasive Alien Species. Global Invasive Species Database. Invasive Species Specialist Group (ISSG), IUCN Species Survival Commission.
  7. ^ a b c d e f g h i "Help push back against the march of yellow crazy ants". Invasive Species Council. 2020-12-17. Retrieved 2020-12-30.
  8. ^ a b c Darras, H.; Berney, C.; Hasin, S.; Drescher, J.; Feldhaar, H.; Keller, L. (April 7, 2023). "Obligate chimerism in male yellow crazy ants". Science. 380 (6640): 55–58. doi:10.1126/science.adf0419. PMID 37023182. S2CID 257985666.
  9. ^ O'Dowd, Dennis J.; Green, Peter T.; Lake, P. S. (2003). "Invasional 'meltdown' on an oceanic island" (PDF). Ecology Letters. 6 (9): 812–817. doi:10.1046/j.1461-0248.2003.00512.x.
  10. ^ "Anoplolepis gracilipes". The Global Ant Biodiversity Informatics (GABI) database. Retrieved 23 January 2019.
  11. ^ a b c Holoway D.A., David A.; Lach, Lori; Suarez, Andrew V.; Tsutsui, Neil D.; Case, Ted J. (2002). "The causes and consequences of ant invasions". Annual Review of Ecology and Systematics. 33: 181–233. doi:10.1146/annurev.ecolsys.33.010802.150444. S2CID 16691880.
  12. ^ McGlynn T.P., Terrence P. (1999). "The Worldwide Transfer of Ants: Geographical Distribution and Ecological Invasions". Journal of Biogeography. 26 (3): 535–548. doi:10.1046/j.1365-2699.1999.00310.x. S2CID 83955798.
  13. ^ a b O’Dowd D.J. (1999). "Crazy Ant Attack". Wingspan. 9 (2): 7.
  14. ^ Bob Yirka. "Yellow crazy ant males have two sets of DNA".
  15. ^ Callaway, Ewen (April 6, 2023). "Crazy ants' strange genomes are a biological first". Nature. doi:10.1038/d41586-023-01002-3. S2CID 258007429 – via www.nature.com.
  16. ^ Ness, J.H.; Bronstein, J.L.; et al. (2004). "The Effects of Invasive Ants on Prospective ant Mutualists". Biological Invasions. 6 (4): 445–461. doi:10.1023/B:BINV.0000041556.88920.dd. S2CID 10180210.
  17. ^ Abbott, Kirsti L.; Green, Peter T.; et al. (2007). "Collapse of an ant-scale mutualism in a rainforest on Christmas Island". Oikos. 116 (7): 1238–1246. doi:10.1111/j.0030-1299.2007.15629.x.
  18. ^ a b Invasive Species Council; (2016) Yellow Crazy Ants In Australia, Invasive Species Council Fact Sheet.
  19. ^ a b c d e Csurhes, Steve and Hankamer, Clare; 2012 (updated 2016) "Invasive Animal Risk Assessment Yellow Crazy Ant"; Queensland Government of Australia. Retrieved 2017-03-17.
  20. ^ Area of Australia – States and Territories. Geoscience Australia
  21. ^ a b c d Hoskin, Conrad and Lach, Lori (2015). "Too much to lose: Yellow crazy ants in the wet tropics" (PDF). Wildlife Australia. 52 (3): 37–41. ISSN 0043-5481.{{cite journal}}: CS1 maint: multiple names: authors list (link)
  22. ^ "Red crab migration". Parks Australia. 2017.
  23. ^ Davis, Naomi; O’Dowd, Dennis; Green, Peter; MacNally, Ralf (15 July 2008). "Effects of an alien ant invasion on abundance, behaviour, and reproductive success of endemic island birds". Conservation Biology. 22 (5): 1165–1176. doi:10.1111/j.1523-1739.2008.00984.x. PMID 18637918. S2CID 36086986.
  24. ^ a b Christmas Island yellow crazy ant control program (PDF). environment.gov.au (Report). Department of the Environment, Australia.
  25. ^ Bittel, Jason (December 24, 2015). "The Christmas crab massacre". nrdc.org. Natural Resources Defense Council.
  26. ^ "Strike team vanquishes crazy ants at Johnston" (PDF). Environment Hawaii Newsletter. Conservation Registry. September 2012.
  27. ^ a b "Yellow crazy ant biological control arrives on Christmas Island". invasives.org.au (blog). 9 January 2017.
  28. ^ Lawler, Susan; Green, Peter (2016-12-02). "The wasp saving Christmas Island's crabs" (Press release). La Trobe University.
  29. ^ Bateman, Daniel (20 May 2016). "Federal funds finally found to combat yellow crazy ants in Far North Queensland". The Cairns Post. Retrieved 2017-03-24.

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wikipedia EN

Yellow crazy ant: Brief Summary

provided by wikipedia EN

The yellow crazy ant (Anoplolepis gracilipes), also known as the long-legged ant or Maldive ant, is a species of ant, thought to be native to West Africa or Asia. They have been accidentally introduced to numerous places in the world's tropics.

The yellow crazy ant has colloquially been given the modifier "crazy" on account of the ant's erratic movements when disturbed. Its long legs and antennae make it one of the largest invasive ant species in the world.

Like several other invasive ants, such as the red imported fire ant (Solenopsis invicta), the big-headed ant (Pheidole megacephala), the little fire ant (Wasmannia auropunctata), and the Argentine ant (Linepithema humile), the yellow crazy ant is a "tramp ant", a species that easily becomes established and dominant in new habitat due to traits such as aggression toward other ant species, little aggression toward members of its own species, efficient recruitment, and large colony size.

It is on a list of "one hundred of the world's worst invasive species" formulated by the International Union for Conservation of Nature (IUCN), having invaded ecosystems from Hawaii to the Seychelles, and formed supercolonies on Christmas Island in the Indian Ocean.

In 2023, a scientific article postulated a for A. gracilipes, suggesting that males are obligate chimeras.

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