Invasive Species Compendium

Detailed coverage of invasive species threatening livelihoods and the environment worldwide


Monomorium destructor
(Singapore ant)



Monomorium destructor (Singapore ant)


  • Last modified
  • 19 November 2019
  • Datasheet Type(s)
  • Invasive Species
  • Pest
  • Preferred Scientific Name
  • Monomorium destructor
  • Preferred Common Name
  • Singapore ant
  • Taxonomic Tree
  • Domain: Eukaryota
  •   Kingdom: Metazoa
  •     Phylum: Arthropoda
  •       Subphylum: Uniramia
  •         Class: Insecta
  • Summary of Invasiveness
  • Monomorium destructor (the Singapore ant) is described as a tramp ant as it is renowned for transporting itself around the world via human commerce and trade. Monomorium destructor is known to cause extensive economic damage in urban...

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Preferred Scientific Name

  • Monomorium destructor (Jerdon, 1851)

Preferred Common Name

  • Singapore ant

Other Scientific Names

  • Atta destructor Jerdon
  • Monomorium basale (Smith)
  • Monomorium gracillimum
  • Monomorium ominosa (Gerstaecker)
  • Myrmica atomaria Gerstaecker
  • Myrmica basalis Smith
  • Myrmica gracillima Smith
  • Myrmica ominosa Gerstaecker
  • Myrmica vexator Smith
  • Parholcomyrmex destructor

International Common Names

  • English: destructive trailing ant

Local Common Names

  • Japan: Mizo-hime-ari

EPPO code

  • MONODE (Monomorium destructor)

Summary of Invasiveness

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Monomorium destructor (the Singapore ant) is described as a tramp ant as it is renowned for transporting itself around the world via human commerce and trade. Monomorium destructor is known to cause extensive economic damage in urban environments by gnawing holes in fabric and rubber goods, removing rubber insulation from electric and phone lines and damaging polyethylene cable. 

Taxonomic Tree

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


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The length of workers is highly variable (Polymorphic) from 1.8 to 3.5mm. The body, from head to post petiole, is uniformly light yellow to dull brownish yellow. The gaster (swollen part of abdomen) is always darker. The head and body are mostly smooth, shining and unsculptured except on the very top of the head, which has fine transverse ridges (which are inconspicuous). The antennae have 12 segments, including a 3-segmented club. Club segments increase in size toward the apex. The eyes of M. destructor are relatively small, with 4-6 ommatidia in the longest rows. Mandibles have 3 strong teeth each; with a fourth tooth that is minute. Sparse body hairs cover the ant (Ferster et al. UNDATED; Harris et al. 2005).

Please click on AntWeb: Monomorium destrutor 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: Singapore 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 Monomorium destructor contains an overview, diagnostic features, comparision charts, images, nomenclature and links. (Sarnat, 2008).


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Native range: India, Ants of Africa (2006) describes the Singapore ant (Monomorium destructor) as 'a tramp species probably of Indian origin'.
Known introduced range: Australasia-Pacific, North America, and South America (Stanley, 2004; Wetterer and O'Hara, 2002; and Hickman and Bieman, 2004).

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: 17 Dec 2021
Continent/Country/Region Distribution Last Reported Origin First Reported Invasive Reference Notes


Congo, Democratic Republic of thePresentIntroduced
South AfricaPresentIntroduced


ChinaPresentPresent based on regional distribution.
Hong KongPresent
-Ryukyu IslandsPresentNative
Sri LankaPresentNative
United Arab EmiratesPresentIntroducedInvasive


SpainPresentPresent based on regional distribution.
-Balearic IslandsPresentIntroduced1992
-Canary IslandsPresentIntroduced

North America

Puerto RicoPresentIntroducedInvasive
United StatesPresentIntroducedInvasive


-Northern TerritoryPresentIntroducedInvasive
-Western AustraliaPresentIntroducedInvasive
Christmas IslandPresentIntroducedInvasive
Cook IslandsPresent
French PolynesiaPresent
New ZealandPresentIntroduced
Papua New GuineaPresent

Sea Areas

Atlantic - Western CentralPresentIntroducedInvasive

South America

EcuadorPresentPresent based on regional distribution.
-Galapagos IslandsPresentIntroducedInvasive


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Singapore ants (Monomorium destructor) nest outdoors or in buildings, depending largely on whether they occur in tropical, semitropical or temperate regions. In northern Western Australia they do not live far from houses where they live above the ground in wall and roof cavities. They are present in some tropical, irrigated, lowland rice fields in the Philippines, and coconut plantations in Sri Lanka. In Florida they nest in soil (lawns) or buildings. On Tiwi Island and in Australia's Northern Territory, M. destructor nests were only associated with urban areas; while there was some spread into surrounding bush land, they appear to be unable to establish in undisturbed habitat. In the United Arab Emirates the ants are present in a wide range of habitats, especially irrigated gardens and disturbed habitats close to water. In the Caribbean they were found nesting in trees in citrus orchards (in hollow twigs and branches) and on the ground (Collingwood et al. 1997; and Harris et al. 2005).

Habitat List

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Terrestrial ManagedDisturbed areas Present, no further details
Terrestrial ManagedUrban / peri-urban areas Present, no further details

Host Plants and Other Plants Affected

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Plant nameFamilyContextReferences
Saccharum officinarum (sugarcane)PoaceaeMain

Biology and Ecology

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The Singapore ant (Monomorium destructor) is a slow moving ant that forages along narrow trails. A generalist with a broad diet of living and dead insects, insect eggs, carbohydrates from tending sap-sucking insects, nectar, seeds; it will forage for sweets, fats and proteins. In households they will feed on almost any food available. M. destructor foragers are slow to find food compared with other tramp ants (Ferster et al. UNDATED; and Harris et al. 2005).

    Lifecycle stages
    Singapore ant (Monomorium destructor) form large colonies with multiple queens (Ferster et al. UNDATED).

      Means of Movement and Dispersal

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      Introduction pathways to new locations
      Other: Most significant is human-mediated dispersal, without which the ant may never have reached its current locations. M. destructor is a tramp ant, renowned for transportation via human commerce and trade. It is associated with a wide range of freight types, making it difficult to target any particular pathways (Harris et al. 2005).
      People sharing resources:M. destructor is a successful tramp species that has become very widely dispersed by trade (Harris et al. 2005).

      Local dispersal methods
      Natural dispersal (local):M. destructor also spreads naturally from established colonies in two ways: colony budding, where queens walk on foot accompanied by workers to a new nesting site; and winged dispersal of inseminated queens to uninfested areas where they start a new colony. This latter mechanism needs to be confirmed; it is most likely colony budding is the primary natural dispersal method (Harris et al. 2005).

        Pathway Causes

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        CauseNotesLong DistanceLocalReferences
        People sharing resources Yes Yes

        Impact Summary

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        Biodiversity (generally) Negative
        Economic/livelihood Negative


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        On a local level (and mostly in urban environments) decreases in ant species diversity have been observed with introductions of the Singapore ant (Monomorium destructor). Outside of urban environments this species is not a major component of ant communities, but it has been documented displacing native invertebrate fauna through aggression, and as such can be a threat to biodiversity. Foragers gnaw holes in fabric and rubber goods, remove rubber insulation from electric and phone lines, and damage polyethylene cable. Cars parked overnight in infested areas can fail to start the next day after the ants have shorted ignition systems. They also forage for sugars, fats and proteins in houses. M. destructor activities can result in high costs in terms of property damage (cars, telecommunication equipment, TVs, etc.) and treatment. Several house and car fires have been attributed to the ant (Harris et al. 2005; and Pacific Invasive Ant Group, 2004).

        Harris et al. 2005 has highlighted the disease-carrying potential of M. destructor, reporting that, a study found bubonic plague bacteria in the faeces of foragers that had fed on plague-infected rats. People being bitten in bed by the ants is very common in the Northern Territory, Australia and is an identifying feature of M. destructor (B. Hoffmann, pers.comm., 2006).

        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.

        Similarities to Other Species/Conditions

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        Monomorium destructor is similar to Monomorium latinode, but is distinguished by the presence of 4 teeth on each mandible (versus 5 in latinode), the distinct metanotal groove (shallow and indistinct in latinode), and the narrower postpetiole (1.5 times as long as broad in latinode).

        Monomorium mayri is separated from M. destructor by its being uniformly dark brown (other characters apparently being near identical); it is recorded from the Sahel countries of western Africa, plus across to Egypt and onwards to West Malaysia (Ants of Africa, 2006).

        Please see Ants of Africa-Monomorium group for high resolution images and detailed description of ants of genus Monomorium including M. destructor and M. mayri. Links to key for genus Monomorium and species from West Africa & the Congo Basin are also available.

          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.

          Preventative measures: 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 (Solenopsis invicta) 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. Monomorium destructor scored as a high-risk threat to New Zealand. The invasive ant risk assessment for M. destructor can be viewed at Monomorium destructor risk assessment. Please see Monomorium destructor information sheet for more information on biology, distribution, pest status and control technologies.

          Chemical: Dried granular corn grit baits are effective against this species. At least three formulations containing 7.3g/kg hydramethylnon (Drax Ant Kil Granular with Hydramethylnon; Garrards Granular Ant Bait; Faslane Granular Ant Bait), and one containing 10 g/kg hydramethylnon (Maxforce Granular Insect Bait) are registered for use against M. destructor in Australia in addition to Amdro (7.3 g/kg hydramethylnon). These baits are also recommended for use against Pheidole megacephala and Solenopsis geminata or ants in general. Engage® (methoprene) and Distance® (pyriproxyfen) have a lipid attractant and are also likely to be attractive to M. destructor. Amdro® has also been used effectively against M. destructor. Ascend® (Affirm®) has been effectively used to control S. invicta and has shown potential to control M. destructor in the field, although some recovery did occur after 2 weeks. Field trials in Malaysia using food attractants found peanut butter was strongly preferred over honey by M. destructor and the use of protein or sugar-based attractants is recommended in baits targeting M. destructor (Stanley, 2004).

          Management Information

          Compiled by the IUCN SSC Invasive Species Specialist Group (ISSG)

          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 management approach remains the most practical strategy for dealing with invasive ants (Krushelnycky Loope and Reimer 2005).
          1.1 Risk Assessments
          The first step to solving any problem is to identify whether it exists and define what it is. Preparing risk assessments is a vital management tool for addressing the issue of invasive ants in a country or region.
          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 M. destructor establishing itself in New Zealand (based on climate similarity of native and introduced ranges) lead to the prediction that it would be unlikely to establish outside but may achieve limited distribution in heated buildings (Harris unpubl. data, in Stanley 2004).
          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).

          2.0 Chemical
          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 affects 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 Bait Design
          Field trials in Malaysia using food attractants found peanut butter (80% of ants) was strongly preferred over honey (20% ants) by M. destructor (Lee 2002, in Stanley 2004). Lee and Kooi (2004, in Stanley 2004) recommend using protein or sugar-based attractants in baits targeting M. destructor. Davis et al. (1993b) found the soybean oil on corn grit bait matrix used is attractive to M. destructor in Western Australia. In food preference tests, plain white bread was the most attractive of a range of food types to M. destructor and was used to monitor ant activity before and after treatments were applied (Davis et al. 1993b).
          2.3 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).
          Amdro® is attractive and effective at controlling M. destructor. Stanley (2004) recommends following bait recommendations for S. invicta (ie: use Distance® (pyriproxyfen) for gradual control and Engage® (methoprene) near water bodies, follow up treatment with Amdro®. Both Engage® (methoprene) and Distance® (pyriproxyfen) have a lipid attractant and are therefore likely to be attractive to M. destructor.
          Davis et al. (1993b, in Stanley 2004) trialled several commercial ant baits developed for S. invicta with the soybean oil on corn grit bait matrix: Finitron® (sulfluramid); Ascend® (abamectin); Award® (fenoxycarb); Amdro®  (hydramethylnon); and Bushwacker® (boric acid in ground shrimp offal bait matrix). Finitron®, followed by Ascend® and Amdro®, were the most effective ant baits, with ant abundance reduced to almost zero (Davis et al. 1993b). However, while there was an untreated ‘control’ plot, there was no replication in this field trial, making it difficult to interpret the results. The efficacy of Finitron®, Ascend® and Amdro® was also tested in replicated laboratory trials with M. destructor colonies (Davis et al. 1993b). Each bait proved equally effective at killing workers while Amdro® caused significantly more queen mortality (75% queen mortality) (Davis et al. 1993b). Finitron® (sulfluramid) has been withdrawn from the US market since the Western Australian trials. The results of these trials resulted in the registration of Amdro® throughout Australia for the control of M. destructor (J. van Scahgen, pers. comm., M. Widmer, pers. comm., in Stanley 2004). At least four formulations containing hydramethylnon (Drax Ant Kil Granular with Hydramethylnon; Garrards Granular Ant Bait; Faslane Granular Ant Bait and Maxforce Granular Insect Bait) are also registered for use against M. destructor in Australia. Several of the more recent commercial baits developed for S. invicta control, such as
          indoxacarb and those containing IGRs, would be likely candidates for the effective control of M. destructor, although this requires testing (Stanley 2004).
          Hickman and Bieman (2004) report effective control of M. destructor with a dual treatment of Termidor for exterior application and Phantom for indoor application.

          3.0 Research
          3.1 Bait and Toxin Research
          Stanley (2004) suggests that future research on W. auropunctata focus on:
          • Trialling the attractiveness and efficacy of Distance® and Engage® on as many high risk species as possible (e.g. S. geminata; M. destructor; W. auropunctata).
          • Comparing the attractiveness and efficacy of Distance®, Engage®, Amdro®, Advion®, Xstinguish® and Chipco Firestar® to verify that S. invicta baits are adequate for M. destructor
          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 responces. 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.

          Harris, R. Undated. Invasive Ant Pest Risk Assessment Project. [Accessed 29 March 2007, from:] This document describes an ant risk assessment and ranking project.
          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]
          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:]
          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:]
          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:]



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          Alpert, G.D. & Wetterer, J.K. (2007). Ants of Samoa. [Accessed 27 March, 2009]

          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.

          AntWeb, 2006. Monomorium destructor AntWeb, 2006. Monomorium destructor

          Butler, G. D., and J. R. L. Usinger. 1963. Insects and other invertebrates from Laysan Island. ATOLL RESEARCH Bulletin NO 98 1963.

          Collingwood, C. A., B. J. Tigar, and D. Agosti. 1997. Introduced ants in the United Arab Emirates. Journal of Arid Environments (1997) 37: 505-512

          Collingwood, C.A. & Van Harten, A. (2001). The ants (Hym., Formicidae) of Niue, South West Pacific. Entomologist's Monthy Lagazine 137: 139-143.

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

          Ferster, B., M. Deyrup, and R. H. Scheffrahn. UNDATED. The Pest Ants of Florida. University of Florida, Fort Lauderdale R.E.C. Fort Lauderdale, FL

          Harris, R. (n.d.). Invasive ant risk assessment: Monomorium destructor. Landcare Research. [Accessed 27 March, 2009]

          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.

          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)

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

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

          Pacific Invasives Initiative (PII), 2006. Feasibility Study for Singapore ant Eradication in Hatohobei State, Republic of Palau.

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

          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.

          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.

          Taylor, R.W. (1967). Entomological survey of the Cook Islands and Niue. 1-Hymenoptera-Formicidae. New Zealand Journal of Science 10(4): 1092-1095.

          The Ants of Africa, 2006. Genus Monomorium - latinode-group, scabriceps-group & destructor-group

          Von Aesch, L. (2006). Introduced Ants in Galápagos (Floreana Island): Importance of Competition, Coexistence and Aggressive Behaviors. Université de Lausanne.

          Walker, K. 2006. Singapore ant (Monomorium destructor) Pest and Diseases Image Library. Updated on 29/08/2006 12:03:32 PM.

          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. (2002). Ants of Tonga. Pacific Science 56(2): 2:125–135.


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          ISSG, 2011. Global Invasive Species Database (GISD). Invasive Species Specialist Group of the IUCN Species Survival Commission.

          Peacock L, 2012. Plants and environment national invasive ant surveillance programme annual report 2011-2012. Surveillance (Wellington), 39(3):70-71.

          Sánchez Soto S, 2013. Presence of Monomorium destructor (Hymenoptera: Formicidae) in Mexico. (Presencia de Monomorium destructor (Hymenoptera: Formicidae) en México.) Fitosanidad, 17(2):97-99.

          Schotman CYL, 1989. Plant pests of quarantine importance to the Caribbean. RLAC-PROVEG, No. 21:80 pp.

          Distribution References

          CABI Data Mining, 2001. CAB Abstracts Data Mining.,

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

          CABI, Undated. CABI Compendium: Status inferred from regional distribution. 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.

          Peacock L, 2012. Plants and environment national invasive ant surveillance programme annual report 2011-2012. Surveillance (Wellington). 39 (3), 70-71.

          Sánchez Soto S, 2013. Presence of Monomorium destructor (Hymenoptera: Formicidae) in Mexico. (Presencia de Monomorium destructor (Hymenoptera: Formicidae) en México.). Fitosanidad. 17 (2), 97-99.

          Schotman C Y L, 1989. Plant pests of quarantine importance to the Caribbean. In: RLAC-PROVEG, 80 pp.

          Seebens H, Blackburn T M, Dyer E E, Genovesi P, Hulme P E, Jeschke J M, Pagad S, Pyšek P, Winter M, Arianoutsou M, Bacher S, Blasius B, Brundu G, Capinha C, Celesti-Grapow L, Dawson W, Dullinger S, Fuentes N, Jäger H, Kartesz J, Kenis M, Kreft H, Kühn I, Lenzner B, Liebhold A, Mosena A (et al), 2017. No saturation in the accumulation of alien species worldwide. Nature Communications. 8 (2), 14435.


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            Reviewed by: Dr Ben Hoffmann - Ant community ecologist CSIRO-TERC Australia
            Compiled by: National Biological Information Infrastructure (NBII) & IUCN/SSC Invasive Species Specialist Group (ISSG)
            Last Modified: Tuesday, October 27, 2009

          Distribution Maps

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