Invasive Species Compendium

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Datasheet

Paratrechina longicornis
(crazy ant)

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Datasheet

Paratrechina longicornis (crazy ant)

Summary

  • Last modified
  • 20 November 2019
  • Datasheet Type(s)
  • Invasive Species
  • Pest
  • Natural Enemy
  • Preferred Scientific Name
  • Paratrechina longicornis
  • Preferred Common Name
  • crazy ant
  • Taxonomic Tree
  • Domain: Eukaryota
  •   Kingdom: Metazoa
  •     Phylum: Arthropoda
  •       Subphylum: Uniramia
  •         Class: Insecta
  • Summary of Invasiveness
  • Paratrechina longicornis, the crazy ant (not to be confused with the yellow crazy ant, Anoplolepis gracilipes) is a tramp ant, which, by definition, is an ant that is widely dispersed through commerce and other human-assisted ave...

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Pictures

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PictureTitleCaptionCopyright
Paratrechina longicornis (crazy ant); Adults. Lam Tsuen Country Park, Hong Kong. October 2017.
TitleAdults
CaptionParatrechina longicornis (crazy ant); Adults. Lam Tsuen Country Park, Hong Kong. October 2017.
Copyright©portioid/via iNaturalist - CC BY-SA 4.0
Paratrechina longicornis (crazy ant); Adults. Lam Tsuen Country Park, Hong Kong. October 2017.
AdultsParatrechina longicornis (crazy ant); Adults. Lam Tsuen Country Park, Hong Kong. October 2017.©portioid/via iNaturalist - CC BY-SA 4.0
Paratrechina longicornis (crazy ant); Adults. Dagny Johnson State Park, Key Largo, Florida, USA. December 2014.
TitleAdults
CaptionParatrechina longicornis (crazy ant); Adults. Dagny Johnson State Park, Key Largo, Florida, USA. December 2014.
Copyright©Judy Gallagher/via Flickr - CC BY 2.0
Paratrechina longicornis (crazy ant); Adults. Dagny Johnson State Park, Key Largo, Florida, USA. December 2014.
AdultsParatrechina longicornis (crazy ant); Adults. Dagny Johnson State Park, Key Largo, Florida, USA. December 2014.©Judy Gallagher/via Flickr - CC BY 2.0
Paratrechina longicornis (crazy ant); Adults. Ezhimala, Payyanur, India. May 2020.
TitleAdults
CaptionParatrechina longicornis (crazy ant); Adults. Ezhimala, Payyanur, India. May 2020.
Copyright©Manoj Karingamadathil (manojkmohan)/via iNaturalist - CC BY-SA 4.0
Paratrechina longicornis (crazy ant); Adults. Ezhimala, Payyanur, India. May 2020.
AdultsParatrechina longicornis (crazy ant); Adults. Ezhimala, Payyanur, India. May 2020.©Manoj Karingamadathil (manojkmohan)/via iNaturalist - CC BY-SA 4.0
Paratrechina longicornis (crazy ant); Colony on Mucuna gigantea seedpod. Honolua Lipoa Point, Maui, Hawaii. April 2018.
TitleColony
CaptionParatrechina longicornis (crazy ant); Colony on Mucuna gigantea seedpod. Honolua Lipoa Point, Maui, Hawaii. April 2018.
Copyright©Forest and Kim Starr/via Starr Environmental - CC BY 4.0
Paratrechina longicornis (crazy ant); Colony on Mucuna gigantea seedpod. Honolua Lipoa Point, Maui, Hawaii. April 2018.
ColonyParatrechina longicornis (crazy ant); Colony on Mucuna gigantea seedpod. Honolua Lipoa Point, Maui, Hawaii. April 2018.©Forest and Kim Starr/via Starr Environmental - CC BY 4.0
Paratrechina longicornis (crazy ant); Adult lateral view. Collected Le Port, Réunion. 2001.
TitleAdult museum specimen
CaptionParatrechina longicornis (crazy ant); Adult lateral view. Collected Le Port, Réunion. 2001.
Copyright©2021 California Academy of Sciences - taken by April Nobile. Specimen: CASENT0063128 from www.antweb.org. Accessed 30 June 2021 - CC BY 3.0
Paratrechina longicornis (crazy ant); Adult lateral view. Collected Le Port, Réunion. 2001.
Adult museum specimenParatrechina longicornis (crazy ant); Adult lateral view. Collected Le Port, Réunion. 2001.©2021 California Academy of Sciences - taken by April Nobile. Specimen: CASENT0063128 from www.antweb.org. Accessed 30 June 2021 - CC BY 3.0
Paratrechina longicornis (crazy ant); Adult dorsal view. Collected Le Port, Réunion. 2001.
TitleAdult museum specimen
CaptionParatrechina longicornis (crazy ant); Adult dorsal view. Collected Le Port, Réunion. 2001.
Copyright©2021 California Academy of Sciences - taken by April Nobile. Specimen: CASENT0063128 from www.antweb.org. Accessed 30 June 2021 - CC BY 3.0
Paratrechina longicornis (crazy ant); Adult dorsal view. Collected Le Port, Réunion. 2001.
Adult museum specimenParatrechina longicornis (crazy ant); Adult dorsal view. Collected Le Port, Réunion. 2001.©2021 California Academy of Sciences - taken by April Nobile. Specimen: CASENT0063128 from www.antweb.org. Accessed 30 June 2021 - CC BY 3.0
Paratrechina longicornis (crazy ant); Adult face close-up. Collected Le Port, Réunion. 2001.
TitleAdult museum specimen
CaptionParatrechina longicornis (crazy ant); Adult face close-up. Collected Le Port, Réunion. 2001.
Copyright©2021 California Academy of Sciences - taken by April Nobile. Specimen: CASENT0063128 from www.antweb.org. Accessed 30 June 2021 - CC BY 3.0
Paratrechina longicornis (crazy ant); Adult face close-up. Collected Le Port, Réunion. 2001.
Adult museum specimenParatrechina longicornis (crazy ant); Adult face close-up. Collected Le Port, Réunion. 2001.©2021 California Academy of Sciences - taken by April Nobile. Specimen: CASENT0063128 from www.antweb.org. Accessed 30 June 2021 - CC BY 3.0
Paratrechina longicornis (crazy ant); Winged adult. West Gulf Drive, Sanibel, Florida, USA. December 2015.
TitleWinged adult
CaptionParatrechina longicornis (crazy ant); Winged adult. West Gulf Drive, Sanibel, Florida, USA. December 2015.
Copyright©Even Dankowicz (edanko)/via iNaturalist - CC BY 4.0
Paratrechina longicornis (crazy ant); Winged adult. West Gulf Drive, Sanibel, Florida, USA. December 2015.
Winged adultParatrechina longicornis (crazy ant); Winged adult. West Gulf Drive, Sanibel, Florida, USA. December 2015.©Even Dankowicz (edanko)/via iNaturalist - CC BY 4.0
Paratrechina longicornis (crazy ant); Adults with scale. Ukumehame, Maui, Hawaii. February 2007.
TitleAdults
CaptionParatrechina longicornis (crazy ant); Adults with scale. Ukumehame, Maui, Hawaii. February 2007.
Copyright©Forest and Kim Starr - Starr Environmental/via Bugwood - CC BY 3.0 US
Paratrechina longicornis (crazy ant); Adults with scale. Ukumehame, Maui, Hawaii. February 2007.
AdultsParatrechina longicornis (crazy ant); Adults with scale. Ukumehame, Maui, Hawaii. February 2007.©Forest and Kim Starr - Starr Environmental/via Bugwood - CC BY 3.0 US
Paratrechina longicornis (crazy ant); Colony on Melaleuca quinquenervia. Kapalua, Maui, Hawaii. June 2002.
TitleColony
CaptionParatrechina longicornis (crazy ant); Colony on Melaleuca quinquenervia. Kapalua, Maui, Hawaii. June 2002.
Copyright©Forest and Kim Starr/via Starr Environmental - CC BY 4.0
Paratrechina longicornis (crazy ant); Colony on Melaleuca quinquenervia. Kapalua, Maui, Hawaii. June 2002.
ColonyParatrechina longicornis (crazy ant); Colony on Melaleuca quinquenervia. Kapalua, Maui, Hawaii. June 2002.©Forest and Kim Starr/via Starr Environmental - CC BY 4.0

Identity

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Preferred Scientific Name

  • Paratrechina longicornis (Latreille, 1802)

Preferred Common Name

  • crazy ant

Other Scientific Names

  • Formica gracilescens Nylander (1856)
  • Formica longicornis Latreille (1802)
  • Formica vagans Jerdon (1851)
  • Paratrechina currens Motschoulsky (1863)
  • Paratrechina longicornis (Latreille) (1925)
  • Prenolepis (Nylanderia) longicornis Emery (1910)
  • Prenolepis longicornis
  • Prenolepis longicornis Roger (1863)
  • Tapinoma gracilescens F. Smith (1858)

International Common Names

  • English: black crazy ant; crazy ant; hairy ant; higenaga-ameiro-ari; long-horned ant; slender crazy ant

EPPO code

  • PAATLO (Paratrechina longicornis)

Summary of Invasiveness

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Paratrechina longicornis, the crazy ant (not to be confused with the yellow crazy ant, Anoplolepis gracilipes) is a tramp ant, which, by definition, is an ant that is widely dispersed through commerce and other human-assisted avenues. The crazy ant’s ability to use many artificial environments is one explanation for its success as an invasive; its mode of reproduction may also contribute towards its invasive success (see ‘Distribution’ and ‘Biology and Ecology’ sections). P. longicornis is extremely easy to identify by observing its rapid and erratic movements. It is highly adaptable to various environments and can be a major pest. It occurs in large numbers in homes or outdoors and is capable of displacing other ants and possibly other invertebrates. It can also negatively affect agriculture by promoting sap-sucking pests, and may spread disease in the hospital environment. P. longicornis forages over long distances away from its nest, making the nest hard to find and the ants difficult to control.

Taxonomic Tree

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  • Domain: Eukaryota
  •     Kingdom: Metazoa
  •         Phylum: Arthropoda
  •             Subphylum: Uniramia
  •                 Class: Insecta
  •                     Order: Hymenoptera
  •                         Family: Formicidae
  •                             Genus: Paratrechina
  •                                 Species: Paratrechina longicornis

Description

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The crazy ant (Paratrechina longicornis) is extremely easy to identify by observing its rapid and erratic movements. The antennae have 12-segments without a club and the scape, the basal segment of the antenna, is extraordinarily long with the apex surpassing the posterior border of the head by at least one-half the scape length. Workers are relatively small (2.3-3mm). Head, thorax, petiole and gaster are dark brown to blackish and the body often has a faint bluish iridescence. All workers in a colony are monomorphic and have only one node between the propodeum and the gaster. Eyes are elliptical, strongly convex, and placed close to the posterior border of the head. Legs are extraordinarily long. The head is elongate and the mandibles narrow. Each mandible has five teeth. A stinger is lacking but P. longicornis may bite an intruder and curve its abdomen forward to inject a formic acid secretion from its acidopore onto the wound. Confirmation of identification may be made with the aid of a hand lens, through which the extremely long antennal scape, long legs and erect setae are very apparent. (Creighton, 1950; Harris and Berry, 2005; Nickerson and Barbara, 2000; and Onoyama and Morisita, 2003).

Please click on AntWeb: Paratrechina longicornis for more images and assistance with identification. The AntWeb image comparison tool lets you compare images of ants at the subfamily, genus, species or specimen level. You may also specify which types of images you would like to compare: head, profile, dorsal, or label.
Please see PaDIL (Pests and Diseases Image Library) Species Content Page Ants: Crazy ant for high quality diagnostic and overview images.

Please follow this link for a fully illustrated Lucid key to common invasive ants [Hymenoptera: Formicidae] of the Pacific Island region [requires the most recent version of Java installed]. The factsheet on Paratrechina longicornis contains an overview, diagnostic features, comparison charts, images, nomenclature and links. (Sarnat, 2008).

 

Distribution

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Paratrechina longicornis is one of the most widely distributed ant species. It is found throughout much of the tropics and subtropics where it is an agricultural and household pest, and is found in temperate zones as an indoor pest. The crazy ant’s widespread distribution is due, at least in part, to its ability to thrive in disturbed and artificial environments including on cargo ships at sea; in addition because they can live indoors in heated houses, their distribution is not restricted by latitude. P. longicornis is rarer in natural undisturbed habitats. It is also less common in inland areas except along major waterways such as the Nile, Congo and Amazon rivers, but P. longicornis may begin to spread more widely inland with increasing air commerce (Wetterer, 2008).

Native range: Africa and Asia (Nickerson and Barbara, 2000); Southeast Asia and Melanesia (Wetterer, 2008). Precise native range is ambiguous since the species has long been recorded as having a widespread distribution.
Known introduced range: Australasia-Pacific Region, Europe, North America, and South America (Andersen et al. 2004; Freitag et al. 2000; Nickerson and Barbara, 2000; and Torres and Snelling, 1997).

Distribution Table

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The distribution in this summary table is based on all the information available. When several references are cited, they may give conflicting information on the status. Further details may be available for individual references in the Distribution Table Details section which can be selected by going to Generate Report.

Last updated: 25 Feb 2021
Continent/Country/Region Distribution Last Reported Origin First Reported Invasive Reference Notes

Africa

AlgeriaPresent1962First reported: 1962
BeninPresent
Cabo VerdePresent1953First reported: 1953
CameroonPresent1916First reported: 1916
Central African RepublicPresent1911First reported: 1911
ComorosPresent1994First reported: 1994
Congo, Democratic Republic of thePresent1901First reported: 1901
EgyptPresent1880First reported: 1880
Equatorial GuineaPresent1940First reported: 1940
EritreaPresent1906First reported: 1906
EthiopiaPresent1933First reported: 1933
GambiaPresent2007First reported: 2007
GhanaPresent1968First reported: 1968
GuineaPresent1876First reported: 1876
KenyaPresentFirst reported: Earliest record < 2004
MadagascarPresent1891First reported: 1891
MaliPresent1970First reported: 1970
MauritiusPresent1942First reported: 1942
-RodriguesPresent1879First reported: 1879
MoroccoPresent1929First reported: 1929
NigeriaPresent1914First reported: 1914
RéunionPresent1895First reported: 1895
Saint HelenaPresentIntroduced1994
-AscensionPresentIntroduced1958
São Tomé and PríncipePresent1920First reported: 1920
SenegalPresent1802First reported: 1802
SeychellesPresent1897First reported: 1897
Sierra LeonePresent1976First reported: 1976
SomaliaPresent1913First reported: 1913
South AfricaPresent1922First reported: 1922
SudanPresent1911First reported: 1911
TanzaniaPresent1912First reported: 1912
UgandaPresent

Antarctica

French Southern TerritoriesPresent1964Europa Island, part of the 'Scattered Islands in the Indian Ocean'; First reported: 1964; Original citation: Wetterer (2008)

Asia

BahrainPresentIntroduced1951
BangladeshPresentIntroduced2005
British Indian Ocean TerritoryPresentIntroduced1971
ChinaPresentIntroduced1921
IndiaPresentIntroduced1851
IndonesiaPresentIntroduced1866
IranPresentIntroduced2000Invasive
IraqPresentIntroduced1917
IsraelPresentIntroduced1880
JapanPresentIntroduced1924
LebanonPresentIntroduced1970
MalaysiaPresentIntroduced1914
MaldivesPresentIntroduced2004
MyanmarPresentIntroduced1887
NepalPresentIntroduced1956
OmanPresentIntroduced1985
PakistanPresentIntroduced2007
PalestinePresent1880First reported: 1880; Original citation: Wetterer (2008)
PhilippinesPresentIntroduced1913
Saudi ArabiaPresentIntroduced1979
SingaporePresentIntroduced1931
Sri LankaPresentIntroduced1858
SyriaPresentIntroduced1880
TaiwanPresentIntroduced1909
ThailandPresentIntroduced1928
United Arab EmiratesPresentIntroduced1995
VietnamPresentIntroduced1920
YemenPresentIntroduced1880

Europe

CzechiaPresentIntroduced1937
DenmarkPresentIntroduced1996
EstoniaPresentIntroduced1887
FrancePresentIntroduced1856
GermanyPresentIntroduced1939Invasive
GibraltarPresentIntroduced1956
GreecePresentIntroduced1988
ItalyPresentIntroduced1981
MaltaPresentIntroduced1975
NetherlandsPresentIntroduced1909
PortugalPresentIntroducedInvasive
-AzoresPresentIntroduced1929Invasive
-MadeiraPresent1859First reported: 1859
SpainPresentIntroduced1998
-Balearic IslandsPresentIntroduced2004
-Canary IslandsPresent1893First reported: 1893
SwedenPresentIntroduced1957
SwitzerlandPresentIntroduced1999
United KingdomPresentIntroducedInvasive

North America

AnguillaPresentIntroduced2006
Antigua and BarbudaPresentIntroduced1918
ArubaPresentIntroduced1994
BahamasPresentIntroduced1904
BarbadosPresentIntroduced1918
BelizePresentIntroduced1906
BermudaPresentIntroduced1990Invasive
British Virgin IslandsPresentIntroducedInvasive
CanadaPresent
-British ColumbiaPresentIntroduced1994
-OntarioPresentIntroduced1978
-QuebecPresentIntroduced1963
Cayman IslandsPresentIntroduced2008
Costa RicaPresentIntroduced1899
CubaPresentIntroduced1876
DominicaPresentIntroduced
Dominican RepublicPresentIntroduced1915
El SalvadorPresentIntroduced1958
GrenadaPresentIntroduced1897
GuadeloupePresentIntroduced1990
GuatemalaPresentIntroduced1911
HaitiPresentIntroduced1907
HondurasPresentIntroduced1916
JamaicaPresentIntroduced1906Invasive
MartiniquePresentIntroduced1913
MexicoPresentIntroduced1859
MontserratPresentIntroduced1934
NicaraguaPresentIntroduced1897
PanamaPresentIntroduced1899Invasive
Puerto RicoPresentIntroduced1906
Saint Kitts and NevisPresentIntroduced1934
Saint LuciaPresentIntroduced1935Invasive
Saint Vincent and the GrenadinesPresentIntroduced1892
Sint MaartenPresent1994First reported: 1994; Original citation: Wetterer (2008)
Trinidad and TobagoPresentIntroduced1895
Turks and Caicos IslandsPresentIntroduced1953
U.S. Virgin IslandsPresentIntroduced1878
United StatesPresent
-AlabamaPresentIntroduced1910
-ArizonaPresentIntroduced1993
-ArkansasPresentIntroducedInvasive
-CaliforniaPresentIntroduced1967Invasive
-FloridaPresentIntroduced1906
-GeorgiaPresentIntroduced1913
-HawaiiPresentIntroduced1887
-IllinoisPresentIntroduced1988
-IndianaPresentIntroduced1921
-LouisianaPresentIntroduced1943
-MarylandPresentIntroduced1913
-MassachusettsPresentIntroduced1928Invasive
-MississippiPresentIntroduced1922
-MissouriPresentIntroduced1901
-New MexicoPresentIntroduced2000
-New YorkPresentIntroduced1886
-North CarolinaPresentIntroduced1937
-OhioPresentIntroduced1998
-OklahomaPresentIntroduced1935
-PennsylvaniaPresentIntroduced1906
-South CarolinaPresentIntroduced1934
-TexasPresentIntroduced1905
-VirginiaPresentIntroduced1915
-WashingtonPresentIntroduced1886

Oceania

AustraliaPresentIntroduced1886
-Northern TerritoryPresentIntroducedInvasive
Christmas IslandPresentIntroduced1933
Cook IslandsPresentIntroduced1925
Federated States of MicronesiaPresentIntroduced1935
FijiPresentIntroduced1920
French PolynesiaPresentIntroduced1907InvasiveWetterer (2008) notes earliest records on Austral Islands (2006) and Tuamotus (1996)
-Marquesas IslandsPresentIntroduced1925
KiribatiPresentIntroduced1914Wetterer (2008) notes earliest record on Banaba Island (1914) and on Gilbert Islands (1957)
-Line IslandsPresent1935First reported: 1935; Original citation: Wetterer (2008)
-Phoenix IslandsPresentIntroducedFirst reported: 1940-41
Marshall IslandsPresentIntroduced1937
New CaledoniaPresentIntroduced1914
New ZealandPresentIntroduced1926
NiuePresentIntroduced1967
Northern Mariana IslandsPresentIntroduced1911
PalauPresentIntroduced1952
Papua New GuineaPresentIntroduced1901
PitcairnPresentIntroduced1934
SamoaPresentIntroduced1870
Solomon IslandsPresentIntroduced1916
Timor-LestePresentIntroduced2005
TokelauPresentIntroduced1924Invasive
TongaPresentIntroduced1923
TuvaluPresentIntroduced1976
United States Minor Outlying Islands
-Wake IslandPresentIntroduced1957
VanuatuPresentIntroduced1930
Wallis and FutunaPresentIntroduced1965

South America

ArgentinaPresentIntroduced1915
BrazilPresentIntroduced1876
ChilePresentIntroduced1859
-Easter IslandPresentIntroduced1971
ColombiaPresentIntroduced1876
EcuadorPresentIntroduced1969
-Galapagos IslandsPresentIntroduced1906Invasive
French GuianaPresentIntroduced1868
GuyanaPresentIntroduced1911
ParaguayPresentIntroduced1997
PeruPresentIntroduced1939
SurinamePresentIntroduced1932
VenezuelaPresentIntroduced1935

Habitat

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The crazy ant (Paratrechina longicornis) is highly adaptable, living in both very dry and rather moist habitats. It often nests some distance away from its foraging area and is usually associated with disturbance. They are a common pest ant in houses and seem peculiarly adapted to the interior and immediate vicinity of human habitations. It nests in places such as trash, refuse, cavities in plants and trees, rotten wood, in soil under objects and nests have also been found under debris left standing in buildings for long periods of time. A crazy ant nest site can be found by looking for workers carrying food back to the nest. P. longicornis can also be found in other environments such as beaches, dry tortugas, geothermal areas, farms and even ships. It is also present in some native vegetation in the tropics, such as in conservation areas on offshore islands. In cold climates, the ants nest in centrally heated buildings. On beaches at high tide, nests can be found submerged underwater and are probably protected from flooding by air trapped in the nest galleries (Harris and Berry, 2005; Longino, 2004; and Nickerson and Barbara, 2000).

Habitat List

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CategorySub-CategoryHabitatPresenceStatus
Terrestrial ManagedCultivated / agricultural land Present, no further details Harmful (pest or invasive)
Terrestrial ManagedDisturbed areas Present, no further details Harmful (pest or invasive)
Terrestrial ManagedUrban / peri-urban areas Present, no further details Harmful (pest or invasive)

Host Plants and Other Plants Affected

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Plant nameFamilyContextReferences
Saccharum officinarum (sugarcane)PoaceaeMain

Biology and Ecology

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Nutrition
Crazy ant (Paratrechina longicornis) foragers are opportunistic omnivores, feeding on live and dead insects, seeds, honeydew, fruits, plant exudates and many household foods. P. longicornis thrive in places such as shops and cafes, where workers may be seen transporting crumbs and insects. They apparently have a seasonal preference for a high-protein diet and during the summer months may refuse honey or sugar baits. They are attracted to honeydew producing hemipterans in spring and autumn/fall. Honeydew is obtained by tending to the hemipternas – e.g. plant lice, mealy bugs and scales – the hemipterans may benefit from being tended by ants; for example, the ants may protect the hemipterans from predators and parasites (Koch et al. 2011). P. longicornis foragers will also collect seeds. Large prey items, such as a lizard, are carried by a highly concerted group action. Workers feed on many household foods, such as meat, grease, sweets, fruits, vegetables and liquids (Smith 1965)" (Harris and Berry, 2005; and Nickerson and Barbara, 2000).

Reproduction
Crazy ant (Paratrechina longicornis) colonies are polygyne. Nests contain up to 2000 workers and 40 queens. Reproduction is throughout the year in warm climates but more restricted in cooler climates. Workers are probably sterile. Colonies occur in temporary nests, are highly mobile, and will move if disturbed. These ants can nest in a variety of locations from dry to moist environments (Harris and Berry, 2005).

Recently, Pearcy et al. (2011) found that P. longicornis has an unusual mode of reproduction whereby workers are produced by normal sexual reproduction, but queens and males are clones of their mothers and fathers respectively.  In this way, the paternal and maternal lines remain distinct and genetically very different from each other; because of this, the sterile workers (which inherit from both the maternal and paternal lines) have high levels of heterozygosity, and this is true even if the queen mates with her brother. This could explain the crazy ant’s invasive success, since worker ants remain heterozygous (i.e. they do not suffer from inbreeding depression) even if produced by a small founder population, as would usually be the case if the species was introduced to a new area on a cargo ship for example.

Lifecycle stages
Crazy ant (Paratrechina longicornis) colonies range from moderate to heavily populous. The colonies may raise sexuals at any time of the year in warmer regions, but in the seasonal climate of north Florida, alate production is apparently limited to the warm rainy months of spring through late summer. On warm, humid evenings, large numbers of males gather outside nest entrances and may mill about excitedly. Workers patrol vegetation and other structures nearby. Periodically, a dealate queen emerges. Trager (1984) has suggested that mating occurs in such groupings around the nest entrance. Wings of queens are removed while still callow and males were never observed to fly or use their wings in any way. However, in several cases it has been observed that males frequently appear at lights (Nickerson and Barbara, 2000).

Means of Movement and Dispersal

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Introduction pathways to new locations
Nursery trade: On 26 October 1990, Greg Mayer, Tina Kuklenski, and Scott Miller sampled invertebrates from a large shipment (an entire barge) of potted plants being unloaded at Guana Island, British Virgin Islands (BVI). The shipment was infested with large numbers of insects and snails, and included P. longicornis (Miller, 1994).
Other: Human-mediated dispersal has helped the spread of P. longicornis at local, regional, national and international scales (Harris et al. 2005). It can be associated with any commodity and transport mode from countries with established populations and is commonly intercepted on air and sea cargo, including fresh produce, timber, empty sea containers and personal baggage (Simon O'Connor pers comm).

Local dispersal methods
Natural dispersal (local): Natural dispersal is primarily by budding. Neither queens nor males appear to fly (Trager 1984). It is a rapid coloniser and often the first species to arrive in a newly disturbed area (Lee 2002) (Harris and Berry, 2005).

Pathway Causes

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CauseNotesLong DistanceLocalReferences
Food Yes
Horticulture Yes
Timber trade Yes

Pathway Vectors

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VectorNotesLong DistanceLocalReferences
Bulk freight or cargo Yes
Luggage Yes
Plants or parts of plants Yes

Impact

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Crazy ant (Paratrechina longicornis) is an extremely hardy species. Its ability to invade a varying degree of habitats makes it a serious threat, and it can occur in large numbers in both homes and outdoors. P. longicornis is a common tramp ant that invades houses and heated buildings, including hospital buildings where it is known to transport pathogenic microbes. (Roxo et al. 2010). It can also be an indirect pest of agriculture, because, it can enhance populations of sap-sucking hemipterans such as aphids and scale insects (see Nutrition in the ‘Biology and Ecology’ section). P. longicornis is capable of displacing other ants and possibly other invertebrates. For example, Koch et al. (2011) suggested that crazy ants in Madagascar could threaten native stingless bee species by competing with them for honeydew.

Risk and Impact Factors

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Invasiveness
  • Highly adaptable to different environments
Impact mechanisms
  • Competition (unspecified)
  • Pest and disease transmission

Uses

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Paratrechina longicornis is involved in an important mutualistic relationship with the eggs of the lizard Mabuya longicaudata in its native range of Taiwan. In high moisture environments reptile eggs are able to condense water on their surfaces. These small water droplets are collected by P. longicornis. When water droplets and P. longicornis were experimentally removed from the eggs of M. longicaudata the eggs were attacked by the egg predator ant Pheidole taivanensis. Both ant species actively searched for the reptilian eggs, with P. taivanensis usually finding eggs first. In the absence of P. longicornis, P. taivanensis predation dramatically reduced lizard egg survival. However when P. longicornis found nests later they were usually able to displace the egg predator ant (Huang, 2008).

Detection and Inspection

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The Pacific Invasive Ant Key (PIAKey) manual Pacific Invasive Ants Taxonomy Workshop Manual can both be used in identifying invasive ants in the Pacific region.

Prevention and Control

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Due to the variable regulations around (de)registration of pesticides, your national list of registered pesticides or relevant authority should be consulted to determine which products are legally allowed for use in your country when considering chemical control. Pesticides should always be used in a lawful manner, consistent with the product's label.

Paratrechina longicornis forages long distances away from the nest and nests can be in cracks in concrete or around wharf piles, which often makes nests difficult to locate and control. (Harris and Berry, 2005; and Nickerson and Barbara, 2000). Many commercially available chemical controls show limited effectiveness, due to difficulties in attracting the ants to chemical baits (Stanley and Robinson, 2007; and see ‘Management Information’ for further details).

Preventative measures: Early detection by active surveillance and subsequent nest treatment is the best way to prevent any ant species from establishing in novel environments. Pitfalls and attractant baits are both methods that can yield good results (Ireneo and Navaareo, 2010; Simon O'Connor pers.comm).

The Pacific Ant Prevention Programme is a proposal prepared for the Pacific Plant Protection Organisation and Regional Technical Meeting for Plant Protection. This plan aims to prevent the red imported fire ant and other invasive ant species with economic, environmental or social impacts from establishing within or spreading between countries in the Pacific.

A detailed pest risk assessment for the eight species ranked as having the highest potential risk to New Zealand (Anoplolepis gracilipes, Lasius neglectus, Monomorium destructor, Paratrechina longicornis, Solenopsis geminata, Solenopsis richteri, Tapinoma melanocephalum, Wasmannia auropunctata) was prepared as part of 'The invasive ant risk assessment project', (Harris et al. 2005)., for Biosecurity New Zealand by Landcare Research. The invasive ant risk assessment for Paratrechina longicornis can be viewed at Paratrechina longicornis risk assessment
Please see Paratrechina longicornis information sheet for more information on biology, distribution, pest status and control technologies.

Cultural control: Non-chemical control is based on exclusion through good housekeeping practices and cleanliness, eliminating food sources. Crazy ants often nest outdoors so prevention of their entrance by caulking exterior penetrations and weather-stripping may aid in their control (Nickerson and Barbara, 2000).

Chemical control: Inside buildings, chemical controls are based on baits, dusts and spot treatments with residual sprays. Outdoor treatments include chemical formulations such as baits, granules, dusts, and sprays (Nickerson and Barbara, 2000).


Management Information

Compiled by IUCN SSC Invasive Species Specialist Group (ISSG)

 
1. Prevention

1.0 Preventative measures

Prevention, quarantine and rapid response are the best management strategies for preventing the establishment of invasive ants. To be successful they require active surveying, early detection and subsequent rapid treatment procedures, often along with quarantines. This type of pro-active management approach remains the most practical strategy for dealing with invasive ants (Krushelnycky, Loope and Reimer, 2005; see also 2.1 Cultural Control).

1.1 Risk Assessments

Risk assessment is a vital management tool for addressing the issue of invasive ants in a country or region. Mapping the potential range of invasive ant species is also a useful tool for assessing risk, preparing risk assessments and estimating the potential threat an invasive ant poses to people and the environment.
In New Zealand an invasive ant risk assessment project (prepared for Biosecurity New Zealand by Landcare Research) identified ant species which pose the greatest potential threat to New Zealand. This project was divided into five sections: (i) gathering data on native and non-native New Zealand ants, (ii) producing a preliminary risk, (iii) producing information sheets on medium-risk and high-risk taxa, (iv) producing a detailed pest risk assessment for the eight highest-risk species, and (v) re-ranking these eight species. Of the 75 ant taxa which were ranked the following ants present the greatest potential risk to New Zealand: Anoplolepis gracilipes, Lasius neglectus, Monomorium destructor, Paratrechina longicornis, Solenopsis geminata, Solenopsis richteri, Tapinoma melanocephalum and Wasmannia auropunctata (Harris undated). An assessment of the current risk of P. longicornis establishing itself in New Zealand (based on climate similarity of native and introduced ranges) led to the prediction that it may establish a limited distribution in non-urban habitat in northern New Zealand, and could establish in and around heated buildings elsewhere (R. Harris unpubl. data, in Stanley 2004). Stanley (2004) also believes that P. longicornis is likely to have a highly restricted distribution in New Zealand.

1.2 Ant Prevention in the Pacific Region

The Pacific island region includes over 25 countries, most of which are served by two important regional international organizations, the Secretariat of the Pacific Community (SPC), which addresses agricultural issues, and the South Pacific Regional Environment Programme (SPREP), which addresses biodiversity issues. The biodiversity of the Pacific is particularly vulnerable to effects of invasive species (SPREP 2000).
Special concern regarding ant invasions has arisen now that the red imported fire ant occurs at or near the coast on both sides of the Pacific, and the little fire ant has arrived in Hawaii and is spreading in the western Pacific. These and other species threaten all Pacific islands, including Hawaii and the U.S. affiliated islands of Guam, Commonwealth of the Northern Marianas, Federated States of Micronesia, American Samoa, and Palau.
The SPC-Plant Protection Service (SPC-PPS) works in partnership with 22 Pacific members to maintain effective quarantine systems and to assist with regionally coordinated eradication/containment efforts. Priorities for emphasis are determined by member countries, which meet periodically as the Pacific Plant Protection Organization (PPPO).
A workshop sponsored by the Invasive Species Specialist Group (ISSG) of IUCN was held in Auckland, New Zealand, in September 2003, and resulted in the compilation of a draft Pacific Ant Prevention Plan (Pacific Invasive Ant Group 2004). The Pacific Ant Prevention Plan was presented to and embraced by 21 Pacific island countries and territories present at a PPPO meeting, the “Regional Biosecurity, Plant Protection and Animal Health” meeting held by SPC in Suva, Fiji, in March 2004 (Pacific Plant Protection Organization 2004). Like Hawaii’s Red Imported Fire Ant Prevention Plan, the Pacific Ant Prevention Plan is still a conceptual work, but ISSG and others are working toward obtaining the international funding needed to implement the plan with the assistance of SPC. The project presents an exceptional opportunity for agriculture and conservation interests to work together with international and bilateral aid entities at regional and country levels to build much needed quarantine capacity. Increased quarantine protection is desperately needed by PICT in order to address invasions that jeopardize both agriculture and biodiversity.
The information for this section was sourced directly from Krushelnycky Loope and Reimer (2005).

 
2. Control

2.1 Cultural Control

Non-chemical control is based on exclusion through good housekeeping practices and cleanliness eliminating food sources. Crazy ants nest outdoors so prevention of their entrance by caulking exterior penetrations and weather-stripping may aid in their control (Nickerson and Barbara 2000).

2.2 Chemical Control
2.2.1 General Considerations

Most if not all ant eradications have employed the use of baits and toxicants, many of which are developed for agriculture or urban settings. However, indiscriminate pesticide use in natural areas and fragile island ecosystems is not advocated. While some toxins such as hydramethylnon break down quickly in the environment, any and all pesticide use is likely to be accompanied by at least some undesirable non-target effects. These include increased runoff or drift outside the intended area, adverse effects on beneficial insects and non-target impacts on native species (Krushelnycky Loope and Reimer 2005).
Non-target impacts must be weighed up carefully against the benefits of ant eradication. Cleary, treating whole ecosystems or islands is too risky as entire populations of rare invertebrates may be at risk of extinction. On the other hand, eradicating populations of exotic ants before they become established in a natural ecosystem or island has the potential to prevent the potentially disastrous consequences of ant invasions (Krushelnycky Loope and Reimer 2005).
Baits should be designed with the specific foraging strategies of the target ant in mind. The preferred size, type and dispersal of bait and the nesting, foraging and behavioural traits of the ant should be considered in the planning stages of the operation. The use of appropriately designed and chosen baits and toxins will help reduce the impact of toxins on native ants and non-target fauna (McGlynn 1999).

2.2.2 Ant Toxins

Ant toxins can be classed into three categories: “stomach” poisons (or metabolic inhibitors), Insect Growth Regulators (IGRs) and neurotoxins. Stomach toxins include hydramethylnon (eg: Maxforce® or Amdro®), sulfuramid and sodium tetraborate decahydrate (eg: Borax). IGRs include compounds such as methoprene, fenoxycarb or pyriproxyfen. Neurotoxins include fipronil (eg: Xstinguish®). Stomach poison kills all workers and reproductives it comes into contact with. IGRs work by disrupting development of the queens ovarian tissues, effectively sterilising the colony. Neurological inhibitors disrupt insect central nervous systems by blocking neuron receptors. The onset of mortality is contingent upon the type of active ingredient. In general, ant baits that contain active ingredients that are metabolic inhibitors have a two to three day delay before extensive mortality occurs in the colony (Oi Vail and Williams 2000). Baits containing IGRs take several weeks before colony populations are reduced substantially (Oi Vail and Williams 2000). The latter (IGRs) provide gradual long-term control, while metabolic inhibitors provide short-term, localised and rapid control (Oi Vail and Williams 2000). This is because while stomach poisons are faster than IGRs, they sometimes eliminate workers before the toxin can be effectively distributed throughout the colony (O’Dowd Green and Lake 1999).
Indoor chemical control is based on baits, dusts or spot treatments with residual sprays. Outdoor treatments include chemical formulations such as baits, granules, dusts and sprays. Read and follow label instructions and precautions before using any insecticide (Nickerson and Barbara 2000).
P. longicornis is notoriously difficult to control with bait (Hedges, 1996a; 1996b; Lee, 2000 in Stanley & Robinson, 2007). It has been reported that it does not feed for long enough on commercial baits to give effective control. Commercial baits are generally designed for control of the red imported fire ant (Solenopsis invicta) and are usually oil based. These baits are not preferred by P. longicornis.
Studies have shown that P. longicornis recruits well to Xstinguish™. HExterm-An-Ant® has also been used against P. longicornis, but although attractive to foragers, its ability to kill queens within the nest is unknown. Trials to compare the attractiveness of Xstinguish™ and Exterm-An-Ant® with other potential options for management of P. longicornis are being conducted in Western Australia"" (Harris et al. 2005).
Stanley (2004) found that the Australian-manufactured IGR baits developed for S. invicta control - Engage® (methoprene) and Distance® (pyriproxyfen) - have a lipid attractant and are unlikely to be attractive to such species as Linepithema humile, T. melanocephalum or P. longicornis. Lee et al. (2003) found some evidence that Protect-B® (0.5% methoprene) baits and Combat Ant Killer® bait stations (1% hydramethylnon) are not effective against P. longicornis (Stanley 2004).
Experiments testing food attractants found P. longicornis strongly preferred honey over peanut butter. Lee and Kooi (2004) report that baiting is seldom effective, particularly with paste and granular formulations, against P. longicornis in Singapore and Malaysia, but recommend sugar-based, liquid or gel formulations for control of P. longicornis. Stanley (2004) recommends using protein and carbohydrate, rather than lipid baits, as the attractants in baits for controlling P. longicornis.
In New Zealand Stanley (2004) recommends using Xstinguish® (fipronil) (already registered and available in New Zealand) in spring and summer as it is expected to be effective at controlling P. longicornis. Liquid boron-based baits <1% toxin) would be expected to be effective in autumn and winter (Stanley 2004).
Further research in New Zealand trialled a range of food types and commercial ant baits (Amdro, Maxforce, Xstinguish, Presto) and boric acid for attractiveness to P. longicornis. The most attractive baits were found to be tuna (no toxin), Xstinguish (non-toxic version), sugar water and sugar water + boric acid. The granular baits (Maxforce, Amdro and Presto) were not as attractive to P. longicornis foragers (Stanley & Robinson, 2007). The authors conclude that “Given that tuna is impractical for management programs, the effectiveness of boric acid, sweet liquid baits in eliminating P. longicornis colonies should be compared with that of the toxic version of Xstinguish. If both are effective at eliminating colonies, we recommend sweet liquid baits containing boric acid be used for small-scale incursions (one or two nests), but a more practicable solid bait, such as Xstinguish, be used for larger scale incursions (numerous nests)”
 

3.0 Research

3.1 Eradication Research

Experimental eradication of ants has been undertaken at several important wildlife refuges in Hawaii’s offshore islets. On Moky Nui (off the windward coast of Oahu, Hawaii) two broadcast applications of Amdro® caused significant declines in S. geminata and P. longicornis, both of which were abundant before treatment (Krushelnycky Loope and Reimer 2005). This small-island experiment is still being evaluated for its efficacy, feasibility and non-target effects and has not lead to standard management practices (Krushelnycky Loope and Reimer 2005).

3.2 Biosecurity New Zealand

Biosecurity New Zealand, the branch of government responsible for managing invasive species, has responded to a series of incursions of exotic invasive ant species by relying heavily on a small number of baits and toxins. The absence of a wide variety of effective baits may compromise the success of incursion responses. As a first step to ensuring effective incursion response, Biosecurity New Zealand commissioned Landcare Research to research and review international literature about the baits and toxins used for ant control (see Stanley 2004). The next step will be testing the most promising of these against a selected group of high-risk invasive ant species.

3.3 Bait and Toxin Research

Stanley (2004) recommends the New Zealand focus research efforts on the species that lack effective strategies and pose some risk to New Zealand (P. longicornis, T. melanocephalum and L. neglectus) to determine which baits can be used to effectively manage them. In an incursion event now, Xstinguish® should be used, but research is required to determine the most effective baits (Stanley 2004).
Stanley (2004) suggests that future research on P. longicornis focus on:
• Determining food preferences and attractants (as there is currently no established best practice for this species)
• Comparing the attractiveness and efficacy of Presto®, Xstinguish® and liquid boron-based baits on P. longicornis.


References
Harris, R. Undated. Invasive Ant Pest Risk Assessment Project. [Accessed 29 March 2007, from: http://issg.appfa.auckland.ac.nz/database/species/reference_files/Ant_RA/overview.pdf]
Krushelnycky, P.D., Loope, L.L. and Reimer, N.J. 2005. The Ecology, Policy, and Management of Ants in Hawaii, Proc. Hawaiian Entomol. Soc. 37. [Accessed 2 April 2007, from: http://www.ctahr.hawaii.edu/peps/museum/ant_website/Krushelnycky_et_al_Ant_review2005.pdf]
Nickerson, J.C., and K.A. Barbara. 2000. Featured Creatures: Crazy Ant: Scientific Name: Paratrechina longicornis (Latreille) (Insecta: Hymenoptera: Formicidae). University of Florida Institute of Food and Agricultural Sciences. Accessed 2 April 2007, from: http://creatures.ifas.ufl.edu/urban/ants/crazy_ant.htm]
O’Dowd, D.J., Green, P.T. and Lake, P.S. 1999. Status, Impact, and Recommendations for Research and Management of Exotic Invasive Ants in Christmas Island National Park. Centre for the Analysis and Management of Biological Invasions: Clayton (Victoria, Australia). [Accessed 4 April 2007, from: http://www.issg.org/database/species/reference_files/Christmas_Island_Report.pdf]
Oi, D.H., Vail, K.M. and Williams, D.F. 2000. Bait distribution among multiple colonies of Pharaoh ants (Hymenoptera: Formicidae), Journal of Economic Entomology 93 (4): 1247 - 1255. [Accessed 13 Friday 2007, from: http://www.bioone.org.ezproxy.auckland.ac.nz/archive/0022-0493/93/4/pdf/i0022-0493-93-4-1247.pdf]
Stanley, M.C. 2004. Review of the Efficacy of Baits Used for Ant Control and Eradication (Landcare Research Contract Report: LC0405/044). [Accessed 29 March 2007, from: http://www.landcareresearch.co.nz/research/biocons/invertebrates/ants/BaitEfficacyReport.pdf]
Stanley, M.C. & Robinson, W.A. (2007). Relative attractiveness of baits to Paratrechina longicornis (Hymenoptera: Formicidae). Journal of Economic Entomology 100 (2): 509-516.

Bibliography

Top of page

Andersen, A. N., J. C. Z. Woinarski, and B. D. Hoffmann. 2004. Biogeography of the ant fauna of the Tiwi Islands, in northern Australia's monsoonal tropics. Australian Journal of Zoology 52:97-110. http://publish.csiro.au/?act=view_file&file_id=ZO03013.pdf

AntWeb, 2006. Paratrechina longicornis http://antweb.org/getComparison.do?rank=species&genus=paratrechina&name=longicornis&project=&project=

Banks, W. A., and D. F. Williams. 1989. Competitive displacement of Paratrechina longicornis (Latreille) (Hymenoptera: Formicidae) from baits by fire ants in Mato Grosso, Brazil. Journal of Entomological Science [J. ENTOMOL. SCI.]. Vol. 24, no. 3, pp. 381-391. 1989. http://www.csa.com/partners/viewrecord.php?requester=gs&collection=ENV&recid=2132095

Blard, F. 2006. Les fourmis envahissantes de l’île de la Réunion : Interaction compétitives et facteurs d’invasion. Thèse de doctorat. Université de la Réunion. 97 pp

Espadaler, X., and V. Bernal. 2003. Exotic ants in the Canary Islands (Hymenoptera, Formicidae). Vieraea. 31 2003. 1-7.

Freitag, A., K. Dorn, and D. Cherix. 2000. First occurrence of the crazy ant Paratrechina longicornis (LATREILLE) (Hym. Formicidae: Formicinae) in Switzerland. Mitteilungen der Schweizerischen Entomologischen Gesellschaft. 73(3-4). 2000. 301-303.

Graham, R. 2006. Crazy Ant (Paratrechina longicornis) Pest and Diseases Image Library. Updated on 29/08/2006 10:34:14 AM. http://www.padil.gov.au/viewPestDiagnosticImages.aspx?id=186

Harris, R. & Abbott, K. (n.d.). Invasive ant risk assessment: Paratrechina longicornis. Landcare Research/MAF Biosecurity New Zealand.

Harris, R.; Abbott, K.; Barton, K.; Berry, J.; Don, W.; Gunawardana, D.; Lester, P.; Rees, J.; Stanley, M.; Sutherland, A.; Toft, R. 2005: Invasive ant pest risk assessment project for Biosecurity New Zealand. Series of unpublished Landcare Research contract reports to Biosecurity New Zealand. BAH/35/2004-1. http://www.landcareresearch.co.nz/research/biocons/invertebrates/Ants/ant_pest_risk.asp

Harris, R.J. & Barker, G. (2007). Relative risk of invasive ants (Hymenoptera: Formicidae) establishing in New Zealand. New Zealand Journal of Zoology 34: 161-178.

Heinze, J. 1986. A New find of Paratrechina longicornis Latreille 1802 on the Azores Portugal Hymenoptera Formicidae. Bocagiana (Funchal).(101). 1986. 1-3.

Hickman, B., and D. Bieman. 2004. Efficacy of Termidor and Phantom on Tropical Ant Complex in Santa Isabel, Puerto Rico.. National Conference on Urban Entomology May 20-22, 2004 Hyatt Regency Phoenix , Arizona.

Hoffmann, Benjamin D and O'Connor, Simon., 2004. Eradication of two exotic ants from Kakadu National Park. Ecological Management & Restoration, August 2004, vol. 5, no. 2, pp. 98-105(8)

Holway, D. A., L. Lach, A. V. Suarez, N. D. Tsutsui, and T. J. Case. 2002. The ecological causes and consequences of ant invasions. Annual review of ecology and systematics 33:181-233.

Huang, W.S. (2008). Resources exploitation by ants facilitates lizard egg survival. Ecological Entomology 33: 555–559.

Jourdan, H., Mille, C. 2006. Les invertébrés introduits dans l'archipel néo-calédonien : espèces envahissantes et potentiellement envahissantes. Première évaluation et recommandations pour leur gestion. In M.-L. Beauvais et al. (2006) : Les espèces envahissantes dans l’archipel néo-calédonien, Paris, IRD Éditions, 260 p.+ cédérom.

Kamura, C.M., Morini, M.S.C.,, Figueiredo, C.J., Bueno, O.C. &Campos-Farinha, A.E.C. (2007). Ant communities (Hymenoptera: Formicidae) in an urban ecosystem near the Atlantic Rainforest. Brazilian Journal of Biology 67(4): 635-641.

Lester, P. J., and A. Tavite. 2004. Long-legged ants, Anoplolepis gracilipes (Hymenoptera: Formicidae), have invaded Tokelau, changing composition and dynamics of ant and invertebrate communities.. Pacific Science, July 2004 v58 i3 p391(11). http://muse.jhu.edu/journals/pacific_science/v058/58.3lester.pdf

Lise, F., Roberto, F., Garcia, M. & Antonio, J. (2006). Association of ants (Hymenoptera: Formicidae) with bacteria in hospitals in the State of Santa Catarina. Revista da Sociedade Brasileira de Medicina Tropical 39(6): 523-526.

Longino, J. T. 2004. Paratrechina longicornis (Latreille 1802). Ants of Costa Rica: The Evergreen State College. http://www.evergreen.edu/ants/genera/paratrechina/species/longicornis/longicornis.html

McGlynn, T.P. 1999. The Worldwide Transfer of Ants: Geographical Distribution and Ecological Invasions, Journal of Biogeography 26(3): 535-548.

Miller, S. E. 1994. Dispersal of Plant Pests into the Virgin Islands. Florida Entomologist 77(4):520.

Neville, P.J., O'Dowd, D.J. & Yen, A.L. (2008). Issues and implications for research on disturbed oceanic islands illustrated through an ant survey of the Cocos (Keeling) Islands. Journal of Insect Conservation 12: 313–323.

Nickerson, J. C., and K. A. Barbara. 2000. Crazy ant: scientific name: Paratrechina longicornis (Latreille) (Insecta: Hymenoptera: Formicidae). Featured Creatures: University of Florida Institute of Food and Agricultural Sciences. http://entomology.ifas.ufl.edu/creatures/urban/ants/crazy_ant.htm

Onoyama, K., and M. Morisita. 2003. Paratrechina longicornis. Japanese Ant Database Group. http://ant.edb.miyakyo-u.ac.jp/E/Taxo/F80502.html

Pacheco, R. & Vasconcelos, H.L. (2007). Invertebrate conservation in urban areas: Ants in the Brazilian Cerrado. Landscape and Urban Planning 81: 193–199.

Pacific Ant Prevention Programme, March 2004. Pacific Invasive Ant Group (PIAG) on behalf of the IUCN/SSC Invasive Species Specialist Group (ISSG).

Pezzatti, B., T. Irzan, and D. Cherix. 1998. Ants (Hymenoptera, Formicidae) of Floreana . Lost Paradise?. From Noticias de Galápagos No.59 April 1998

Rizo, J. J. F. 1993. Ant fauna from Isla de la Juventud and from some keys of the Cuban Archipelago. Poeyana Instituto de Ecologia y Sistematica Academia de Ciencias de Cuba. 0(444). 1993. 1-7.

Sarnat, E. M. (December 4, 2008) PIAkey: Identification guide to ants of the Pacific Islands, Edition 2.0, Lucid v. 3.4. USDA/APHIS/PPQ Center for Plant Health Science and Technology and University of California — Davis. http://www.lucidcentral.org/keys/v3/PIAkey/index.html

Schembri, S. P., and C. A. Collingwood. 1981. A Revision of the Myrmeco fauna of the Maltese Island Hymenoptera Formicidae . del Museo Civico di Storia Naturale "Giacomo Doria". 83 1980, 1981. 417-442.

Stanley, M. C. 2004. Review of the efficacy of baits used for ant control and eradication. Landcare Research Contract Report: LC0405/044. Prepared for: Ministry of Agriculture and Forestry. http://www.landcareresearch.co.nz/research/biocons/invertebrates/ants/BaitEfficacyReport.pdf

Stewart, J. 2003. Crazy Ant Species Found . Biosecurity New Zealand.

Tinaut, A., and J. Luis Ano. 2000. Paratrechina longicornis, a new record for the Iberian Peninsula (Hymenoptera, Formicidae). Boletin de la Asociacion Espanola de Entomologia. 24(1-2). Junio, 2000. 253-254.

Torres, J. A., and R. R. Snelling. 1997. Biogeography of Puerto Rican ants: a non-equilibrium case? Biodiversity and Conservation 6, 1103±1121 (1997).

Wetterer, J. K. 2002. Ants of Tonga (1). (Statistical Data Included).Pacific Science, April 2002 v56 i2 p125(11).

Wetterer, J. K., and A. L. Wetterer. 2004. Ants (Hymenoptera: Formicidae) of Bermuda. Florida Entomologist 87(2):212-221. http://www.fcla.edu/FlaEnt/fe87p212.pdf

Wetterer, J. K., and B. C. O'Hara. 2002. Ants (Hymenoptera: Formicidae) of the Dry Tortugas, The outermost Florida Keys. Florida Entomologist 85(2):303-307.

Wetterer, J.K. & Keularts, J.L.W. (2008). Population explosion of the hairy crazy ant Paratrechina pubens (Hymenoptera: Formicidae) on St. Croix, US Virgin Islands. Florida Entomologist 91(3): 423-427.

Wetterer, J.K. (2008). Worldwide spread of the longhorn crazy ant, Paratrechina longicornis (Hymenoptera: Formicidae) Myrmecological News 11: 137-149.

Wetterer, J.K., Espadaler, X., Ashmole, P., Mendel, H., Cutler, C. & Endeman, J. (2007). Ants (Hymenoptera: Formicidae) of the South Atlantic islands of Ascension Island, St Helena, and Tristan da Cunha. Myrmecological News 10: 29-37.

Wetterer, J.K., Espadaler, X., Wetterer, A.L., Aguin-Pombo, D. & Franquinho-Aguiar, A.M. (2006). Long-term impact of exotic ants on the native ants of Madeira. Economic Entomology 31: 358–368.

Wilson, E. O. 1973. The Ants of Easter Island and Juan-Fernandez. Pacific Insects. 15(2). 1973. 285-287.

References

Top of page

Ireneo L; Navaaero MV, 2010. Effectiveness of thiamethoxam gel bait against the black crazy ant, Paratrechina longicornis (Latreille). The Philippine Entomologist, 24:77-86.

ISSG, 2011. Global Invasive Species Database (GISD). Invasive Species Specialist Group of the IUCN Species Survival Commission. http://www.issg.org/database

Koch H; Corcoran C; Jonker M, 2011. Honeydew collecting in Malagasy stingless bees (Hymenoptera: Apidae: Meliponini) and observations on competition with invasive ants. African Entomology, 19(1):36-41. http://journals.sabinet.co.za/essa

Krauss U, 2012. 161 Invasive Alien Species present in Saint Lucia and their current status. Caribbean Alien Invasive Species Network (CIASNET), 12 pp. http://www.ciasnet.org/wp-content/uploads/2010/08/IAS-present-in-SLU-May-2012-revision.pdf

Lokeshwari D; Kumar NKK; Manjunatha H, 2015. Record of ants (Hymenoptera: Formicidae) tending aphids with special reference to the melon aphid, Aphis gossypii Glover (Hemiptera: Aphididae). Pest Management in Horticultural Ecosystems, 21(1):31-37. http://aapmhe.in/index.php/pmhe/article/view/289/270

Peacock L, 2012. Plants and environment national invasive ant surveillance programme annual report 2011-2012. Surveillance (Wellington), 39(3):70-71. http://www.biosecurity.govt.nz/publications/surveillance/index.htm

Pearcy M; Goodisman MD; Keller L, 2010. Sib mating without inbreeding in the longhorn crazy ant. Proceedings of the Royal Society B:10.1098/rspb.2010.

Roxo E; Campos AEC; Alves MP; Couceiro APMR; Harakava R; Ikuno AA; Ferreira VCA; Baldassi L; Almeida EA; Spada DTA; Augusto M; Melo FAF, 2010. Ants' role (Hymenoptera: Formicidae) as potential vectors of mycobacteria dispersion. Arquivos do Instituto Biológico (São Paulo), 77(2):359-362. http://www.biologico.sp.gov.br/docs/arq/v77_2/roxo.pdf

Stanley MC; Robinson WA, 2007. Relative attractiveness of baits to Paratrechina longicornis (Hymenoptera: Formicidae). Journal of Economic Entomology, 100(2):509-516. http://www.bioone.org/doi/full/10.1603/0022-0493%282007%29100%5B509%3ARAOBTP%5D2.0.CO%3B2

Wetterer JK, 2008. .

Distribution References

Agboton C, Onzo A, Ouessou F I, Goergen G, Vidal S, Tamò M, 2014. Insect fauna associated with Anacardium occidentale (Sapindales: Anacardiaceae) in Benin, West Africa. Journal of Insect Science (Annapolis). 14 (229), 1-11. http://www.bioone.org/doi/full/10.1093/jisesa/ieu091

CABI Data Mining, Undated. CAB Abstracts Data Mining.,

CABI, Undated. Compendium record. Wallingford, UK: CABI

CABI, Undated a. CABI Compendium: Status as determined by CABI editor. Wallingford, UK: CABI

Invasive Species Specialist Group (ISSG), 2011. Global Invasive Species Database (GISD). In: Global Invasive Species Database (GISD), Auckland, New Zealand: University of Auckland. http://www.issg.org/database

Krauss U, 2012. 161 Invasive Alien Species present in Saint Lucia and their current status. In: Caribbean Alien Invasive Species Network (CIASNET), 12 pp. http://www.ciasnet.org/wp-content/uploads/2010/08/IAS-present-in-SLU-May-2012-revision.pdf

Lokeshwari D, Kumar N K K, Manjunatha H, 2015. Record of ants (Hymenoptera: Formicidae) tending aphids with special reference to the melon aphid, Aphis gossypii Glover (Hemiptera: Aphididae). Pest Management in Horticultural Ecosystems. 21 (1), 31-37. http://aapmhe.in/index.php/pmhe/article/view/289/270

Peacock L, 2012. Plants and environment national invasive ant surveillance programme annual report 2011-2012. Surveillance (Wellington). 39 (3), 70-71. http://www.biosecurity.govt.nz/publications/surveillance/index.htm

Vanderhaegen K, Naturinda Z, Kouakou L M M, Vanderheyden A, Dekoninck W, 2019. First record of the invasive longhorn crazy ant, Paratrechina longicornis (Latreille, 1802) (Hymenoptera: Formicidae) from Mt. Elgon, eastern Uganda. BioInvasions Records. 8 (3), 505-514. DOI:10.3391/bir.2019.8.3.05

Links to Websites

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WebsiteURLComment
GISD/IASPMR: Invasive Alien Species Pathway Management Resource and DAISIE European Invasive Alien Species Gatewayhttps://doi.org/10.5061/dryad.m93f6Data source for updated system data added to species habitat list.
Global register of Introduced and Invasive species (GRIIS)http://griis.org/Data source for updated system data added to species habitat list.

Contributors

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    Reviewed by: Simon O'Connor Coordinator, Pacific Ant Prevention Programme Secretariat of the Pacific Community New Zealand
      Compiled by: National Biological Information Infrastructure (NBII) & IUCN/SSC Invasive Species Specialist Group (ISSG)Updates with support from the Overseas Territories Environmental Programme (OTEP) project XOT603, a joint project with the Cayman Islands Government - Department of Environment

      Last Modified: Monday, October 04, 2010

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