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Datasheet

Acanthaster planci
(crown-of-thorns starfish)

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Datasheet

Acanthaster planci (crown-of-thorns starfish)

Summary

  • Last modified
  • 20 November 2019
  • Datasheet Type(s)
  • Invasive Species
  • Preferred Scientific Name
  • Acanthaster planci
  • Preferred Common Name
  • crown-of-thorns starfish
  • Taxonomic Tree
  • Domain: Eukaryota
  •   Kingdom: Metazoa
  •     Phylum: Echinodermata
  •       Class: Stelleroidea
  •         Subclass: Asteroidea
  • Summary of Invasiveness
  • Coral gardens from Micronesia and Polynesia provide valuable marine resources for local communities and environments for native marine species such as marine fish. In coral ecosystems already affected by coral bleachi...

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Pictures

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PictureTitleCaptionCopyright
Crown of Thorns starfish (Acanthaster planci) on a Porites cylindrica colony; Mariana Islands, Guam. Image courtesy of David Burdick/NOAA - http://www.photolib.noaa.gov/
TitleCrown of thorns starfish
CaptionCrown of Thorns starfish (Acanthaster planci) on a Porites cylindrica colony; Mariana Islands, Guam. Image courtesy of David Burdick/NOAA - http://www.photolib.noaa.gov/
CopyrightDavid Burdick/NOAA
Crown of Thorns starfish (Acanthaster planci) on a Porites cylindrica colony; Mariana Islands, Guam. Image courtesy of David Burdick/NOAA - http://www.photolib.noaa.gov/
Crown of thorns starfishCrown of Thorns starfish (Acanthaster planci) on a Porites cylindrica colony; Mariana Islands, Guam. Image courtesy of David Burdick/NOAA - http://www.photolib.noaa.gov/David Burdick/NOAA

Identity

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Preferred Scientific Name

  • Acanthaster planci

Preferred Common Name

  • crown-of-thorns starfish

International Common Names

  • English: coral-eating starfish; coral-feeding starfish; crown of thorns starfish; giant thorny starfish

Local Common Names

  • Palau: rrusech

Summary of Invasiveness

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Coral gardens from Micronesia and Polynesia provide valuable marine resources for local communities and environments for native marine species such as marine fish. In coral ecosystems already affected by coral bleaching, excess tourism and natural events such as storms and El Nino, the effects of the invasive crown-of-thorns starfish (Acanthaster planci) on native coral communities contributes to an already dire state of affairs. Acanthaster planci significantly threatens the viability of these fragile coral ecosystems, and damage to coral gardens by the starfish has been quite extensive in some reef systems. Outbreaks in the Pacific appear to be more massive and widespread than those elsewhere. This may reflect different patterns of outbreak between Pacific and Indian Ocean populations, which have recently been shown to form separate clades of an A. planci species complex. (Vogler et al. 2008; and see 'Description' section).

Taxonomic Tree

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  • Domain: Eukaryota
  •     Kingdom: Metazoa
  •         Phylum: Echinodermata
  •             Class: Stelleroidea
  •                 Subclass: Asteroidea
  •                     Order: Valvatida
  •                         Family: Acanthasteridae
  •                             Genus: Acanthaster
  •                                 Species: Acanthaster planci

Description

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Recent molecular analysis has shown that Acanthaster planci is in fact a species complex consisting of four distinct clades from the Red Sea, the Pacific, the Northern and the Southern Indian Ocean. Benzie (1999) had previously demonstrated the genetic differentiation between A. planci from the Pacific and the Indian Ocean, and this genetic grouping is reflected in the distribution of colour morphs: grey-green to red-brown in the Pacific Ocean, and blue to pale red in the Indian Ocean (Benzie, 1999). Colour combinations can vary from purplish-blue with red tipped spines to green with yellow-tipped spines (Moran, 1997). Those on the Great Barrier Reef are normally brown or reddish grey with red-tipped spines, while those in Thailand are a brilliant purple (Moran, 1997). Adult A. planci usually range in diameter from around 20 to 30cm (PERSGA/GEF 2003) although specimens of up to 60cm (and even 80cm) in total diameter have been collected (Chesher, 1969; Moran, 1997). The juvenile starfish begins with 5 arms and develops into an adult with an astounding 16 to 20 arms, all heavily armed with poisonous spines 4 to 5cm in length, which can inflict painful wounds (Moran, 1997; Birk, 1979). Arm values vary between localities with a range of 14 to 18cm given for the Great Barrier Reef (Moran 1997). Starfish are usually concealed during daylight hours, hiding in crevices (Brikeland and Lucas, 1990; Chesher, 1969). Groups of starfish often move as huge masses of 20 to 200 individuals, presenting a terrifying "front" which destroys the reef as it moves through (Chesher, 1969). Signs of starfish presence are obvious; the coral skeleton is left behind as the result of starfish feeding and stands out sharply as patches of pure white, which eventually become overgrown with algae (Chesher, 1969). In some cases, herbivorous sea urchins move in to feed on algae, creating a pattern against the white coral that resembles the holes of swiss cheese (Tsuda et al. 1970).

Distribution

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The geographical range of Acanthaster planci extends from Mauritius in the western Indian Ocean, including the Red Sea, across the Pacific to the west coast of America (Sladen 1889, in Birkeland and Lucus 1990).

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: 10 Jan 2020
Continent/Country/Region Distribution Last Reported Origin First Reported Invasive Reference Notes

Africa

EgyptPresentInvasiveInvasive Species Specialist Group (ISSG) (2011)
KenyaPresentAppeltans et al. (2012)
MadagascarPresentInvasiveInvasive Species Specialist Group (ISSG) (2011)Also found at the Mascarene Basin (Appeltans et al. 2012)
MauritiusPresentInvasiveInvasive Species Specialist Group (ISSG) (2011)Also recorded at Cargados Carajos Shoals, northeast of Mauritius (Appeltans et al. 2012)
MozambiquePresentAppeltans et al. (2012)
SeychellesPresentAppeltans et al. (2012)
-Aldabra IslandsPresentCABI (Undated a)
South AfricaPresentInvasive Species Specialist Group (ISSG) (2011)
SudanPresentInvasive Species Specialist Group (ISSG) (2011)
TanzaniaPresentAppeltans et al. (2012)

Asia

British Indian Ocean Territory
-Chagos ArchipelagoPresentAppeltans et al. (2012)
Cocos IslandsPresentInvasiveInvasive Species Specialist Group (ISSG) (2011)
IndiaPresentInvasiveInvasive Species Specialist Group (ISSG) (2011)
IndonesiaPresentInvasiveInvasive Species Specialist Group (ISSG) (2011)
-Irian JayaPresentInvasive Species Specialist Group (ISSG) (2011)
-SulawesiPresentInvasive Species Specialist Group (ISSG) (2011)
JapanPresentInvasive Species Specialist Group (ISSG) (2011)
-Ryukyu IslandsPresentInvasiveInvasive Species Specialist Group (ISSG) (2011)
MalaysiaPresentCABI (Undated)Present based on regional distribution.
-Peninsular MalaysiaPresentInvasive Species Specialist Group (ISSG) (2011)
-SabahPresentInvasiveInvasive Species Specialist Group (ISSG) (2011)
MaldivesPresentInvasive Species Specialist Group (ISSG) (2011)
OmanPresentInvasiveInvasive Species Specialist Group (ISSG) (2011)
PhilippinesPresentInvasive Species Specialist Group (ISSG) (2011)An outbreak in 2009 affected the Tubbataha reef, Sulu Sea; a UNESCO World Heritage Site (Bos, 2010).
Saudi ArabiaPresentInvasiveInvasive Species Specialist Group (ISSG) (2011)
ThailandPresentInvasive Species Specialist Group (ISSG) (2011)

North America

Costa RicaPresentInvasive Species Specialist Group (ISSG) (2011)
PanamaPresentInvasive Species Specialist Group (ISSG) (2011)
United StatesPresentCABI (Undated)Present based on regional distribution.
-HawaiiPresentInvasive Species Specialist Group (ISSG) (2011)

Oceania

American SamoaPresentInvasiveInvasive Species Specialist Group (ISSG) (2011)
AustraliaPresentInvasiveInvasive Species Specialist Group (ISSG) (2011)
-Lord Howe IslandPresentInvasive Species Specialist Group (ISSG) (2011)
-Northern TerritoryPresentInvasive Species Specialist Group (ISSG) (2011)
-QueenslandPresentInvasiveInvasive Species Specialist Group (ISSG) (2011)
-Western AustraliaPresentInvasive Species Specialist Group (ISSG) (2011)
Cook IslandsPresentInvasiveInvasive Species Specialist Group (ISSG) (2011)
FijiPresentInvasiveInvasive Species Specialist Group (ISSG) (2011)
French PolynesiaPresentInvasiveInvasive Species Specialist Group (ISSG) (2011)
GuamPresentInvasiveInvasive Species Specialist Group (ISSG) (2011)
Marshall IslandsPresentInvasiveInvasive Species Specialist Group (ISSG) (2011)
New ZealandPresentCABI (Undated)Present based on regional distribution.
-Kermadec IslandsPresentInvasiveInvasive Species Specialist Group (ISSG) (2011)
Northern Mariana IslandsPresentInvasiveInvasive Species Specialist Group (ISSG) (2011)
PalauPresentInvasiveInvasive Species Specialist Group (ISSG) (2011)
Papua New GuineaPresentInvasiveInvasive Species Specialist Group (ISSG) (2011)
SamoaPresentInvasiveInvasive Species Specialist Group (ISSG) (2011)
VanuatuPresentInvasive Species Specialist Group (ISSG) (2011)

Sea Areas

Indian Ocean - WesternPresentInvasiveInvasive Species Specialist Group (ISSG) (2011)
Pacific - Western CentralPresentInvasiveInvasive Species Specialist Group (ISSG) (2011)

South America

ColombiaPresent2010Narváez and Zapata (2010)Malpelo Island

Habitat

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The crown-of-thorns starfish (A. planci) is limited by the location of its food source, coral, from just below spring tide level to a depth limit of 65 metres (Chesher, 1969). Soft substrate is avoided by the crown-of-thorns starfish as it lacks a gripping surface for the tube feet to hold on to (Chesher, 1969). In areas of strong wave action, sand can provide a barrier to movement of the starfish between reef patches (Chesher, 1969). The starfish prefers to live in more sheltered areas, such as lagoons, and in deeper water along reef fronts (Moran, 1997). They generally avoid shallow water on the tops of reefs, where the water conditions are likely to be more turbulent (Moran, 1997). When the weather is calm the potential range of the starfish increases and the starfish may cross sand patches and may feed in shallow water areas (Chesher, 1969; Moran, 1997).

Habitat List

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CategorySub-CategoryHabitatPresenceStatus
Marine Present, no further details Harmful (pest or invasive)

Biology and Ecology

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Nutrition

Acanthaster planci larvae feed on phytoplankton (Birkeland, 1982) and dissolved organic matter (Hoegh-Guldberg, 1994). Once they have developed into juvenile starfish they feed on encrusting algae (Moran, 1997). Adult Acanthaster planci feed primarily on coral, hence one of its names (coral-feeding starfish). The starfish feeds on polyps of corals by everting its stomach and secreting enzymes (Birk, 1979). Other animals feed on coral but none so efficiently as Acanthaster planci (Chesher, 1969), which is aptly referred to as a "corallivore" and spends on average about 45% of its time feeding (De'ath and Moran, 1998). A single starfish of Acanthaster planci can graze ten square metres a year of coral (Vicente, 1999). Measurement of feeding rates of Acanthaster planci have shown that feeding rates in summer are about twice that in winter, but are significantly depressed following the summer spawning season (Keesing and Lucas, 1992). In the laboratory, specimens have eaten molluscs and echinoderms, however scleractinian corals are their primary prey (Chesher, 1969). Scleractinia is an order of coral known as stony or hard corals which is made up of 18 families. Preferred species in the Western Pacific include Montipora spp., Acropora spp. and other members in the Acroporidae and Pocilloporidae families (Colgan, 1987; Quinn and Kojis, 2003). Acropora gemmifera, A. nasuta, A. loripes, Seriatopora hystrix, Pocillopora damicornis and Stylophora pistillata are preferred species too, however, they are protected by mutualistic crustaceans (see notes) (Colgan 1987; Glynn, 1976, 1980, 1983, in Colgan, 1987; Pratchett, 2001). In French Polynesia, Acanthaster planci show a feeding preference for all growth-forms of Acropora as well as the genus Montipora and Pocillopora (Faure, 1989).

Reproduction

Sexes are separate and females release huge amounts of gametes directly into the sea (Benzie, 1999). An individual female Acanthaster planci can produce up to 60 million eggs per year (Conand, 1985, in Babcock and Mundy, 1992). If conditions are favourable and there is an abundant larval survival, the high reproductive potential of even a few adult A. planci may allow the production of a massive settlement of juveniles (Birkeland, 1982). According to data derived from one location in the Great Barrier Reef, Australia, major spawning occurred in December 1991, with smaller spawning events following in January (Babcock and Mundy, 1992). Over two-thirds of the population aggregate to participate in this spawning event, which usually occurs in the morning or afternoon and may be driven by pheromones released into currents (Babcock and Mundy, 1992). A. planci often spawns in a characteristic arched posture, usually on top of elevated rocks or corals at elevations of 30m to reefs flats (Babcock and Mundy, 1992). Migration to shallow water is commonly associated with A. planci spawning (Babcock et al. 1994). Babcock and Mundy (1992) recorded 47% fertilisation rates between animals separated by 32m and 23% for animals separated by over 60m. Fertilisation rates achieved are two orders of magnitude greater than those recorded for other marine organisms, due to the large amounts of gametes produced (Babcock and Mundy, 1992).

Lifecycle stages

After the gametes (eggs and sperms) and hormones (which stimulate other individuals to release gametes) of A. planci are shed into the seawater the gametes have a short amount of time to become fertilised before they become unviable (Madl, 1998). After fertilisation, the zygote develops into a larva. After drifting around for two to three weeks, the 0.5mm small larva starts to morph and eventually settles and attaches itself to the sea floor where it completes its metamorphosis (Madl, 1998). Larval life may last longer than three weeks if conditions are unfavourable (Birkeland and Lucus, 1990, in Benzie, 1999). Various substrates, particularly crustose coralline algae with bacterial surface films, induce Acanthaster's planktonic larvae to settle and metamorphose (Johnson and Cartwright, 1996). One group of scientists found that thyroxine accelerates development in Acanthaster through larval stages (Johnson and Cartwright, 1996). After settlement, the larva metamorphoses into a juvenile starfish, a process which takes about two days (Moran, 1997). Initially the juvenile starfish has only five rudimentary arms, but additional arms develop rapidly as the starfish begins to feed on encrusting algae (Moran, 1997). At the end of six months, the starfish is about 1cm in size and begins to feed on corals (Moran, 1997). Individuals are able to reproduce after two years (Lucas, 1973, in Babcock and Mundy, 1992). Being a rapid grazer of coral polyps, it takes only three to four years for the crown-of-thorns starfish to reach a reasonable size of 30-35cm (Madl, 1998). After three to four years, it is thought to go into a senile phase where growth declines dramatically and reproduction is low (Moran, 1997). It is not known how long the starfish live, although they have been kept in aquaria for as long as eight years (Moran, 1997).

Associations

An interesting example of mutualism has been described between the sessile branching pocilloporid corals, which obviously have a limited behavioural capacity to fend off enemies, and crustacean species. The crab Trapezia ferruginea and the shrimp Alpheus lottini live on the coral as symbionts and are protected by coral mucus from predators. In return, they protect corals from enemy attacks, including predation by the crown-of-thorns starfish, Acanthaster planci (Glynn, 1976, in Hay et al. 2004). Species the starfish would readily feed on if it weren't for the presence of these mutualistic crustaceans include: Acropora gemmifera, A. nasuta, A. loripes, Seriatopora hystrix, Pocillopora damicornis and Stylophora pistillata (Pratchett, 2001).

Means of Movement and Dispersal

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Natural dispersal (local): Tagged specimens of A. planci move as far as 250m per week but feeding starfish move slower (Chesher 1969). Strong surges and high wave action can slow colonisation of new reef sites (Chesher 1969).
Water currents:Acanthaster larvae are carried by currents to widely-scattered areas, as has been the case in the Ryukyus (Japan) (Yamaguchi, 1986, in Nakamura 1986).

Pathway Vectors

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VectorNotesLong DistanceLocalReferences
Water Yes Yes Timmers et al., 2011

Impact Summary

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CategoryImpact
Biodiversity (generally) Negative
Economic/livelihood Negative

Impact

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Predation of corals by Acanthaster planci, storm damage, coral diseases and temperature-related stresses were the most commonly recorded natural impacts to coral reefs. The impact of crown-of-thorns starfish on natural coral assemblages can be severe and long-lasting. In some reefs 90% of live coral cover is lost.

General Impacts

Original text compiled by IUCN SSC Invasive Species Specialist Group (ISSG)

 Since the 1960’s outbreaks of the crown-of-thorns starfish Acanthaster planci have been recorded throughout the Indo-Pacific region. From the time these outbreaks were first recorded, it has been recognised that they pose a threat to the viability of coral reef habitats and the creatures that depend on them. The impact of outbreaks of the crown-of-thorns starfish on natural coral assemblages can be severe and long-lasting. On some reefs up to 90% of live coral cover has been lost, as was the case in areas of Saipan (Tsuda et al. 1970), the Marshall Islands (Pinca et al. Undated) and Guam (Chesher 1969). The impact of outbreaks can be profound. For example the branching corals of Iriomote Island (Ryukyu Islands, Japan) were completely decimated by A. planci and replaced by flat plains of rubble, significantly lower in fish diversity (Sano 2000). Similarly coral gardens at Tanguisson Reef (Guam) were devastated following the 1960s outbreak of the crown-of-thorns starfish and the composition of coral communities shifted from preferred prey species such as Montipora and Acropora to non-preferred prey species such as Porites, Millepora and Leptastrea (Colgan 1987). A study by Cameron, Endean and De Vantier (1991) found that coral structure was significantly different between A. planci affected and non-affected sites. Members of the Poritidae family were predominant on outbreak-affected reefs, while members of the Faviidae family were predominant on non-outbreak reefs. In addition few large (old) colonies occurred on the outbreak reefs, whereas such large corals were common on unaffected reefs. On the Great Barrier Reef and elsewhere significantly higher abundances of turf algae are found to occur on reefs affected by starfish predation in comparison with live coral (Hart and Klumpp 1996). Fortunately, secondary invasion by competitively strong groups of macro-benthos, such as soft corals or macro-algae, appears not to be a limiting factor when it comes to coral recovery (Fabricius 1996).

The changes in coral composition mentioned in the last paragraph may be long-lasting, as is the case in the western Pacific Islands of Rota, Saipan and Tinian where non-preferred coral prey such as Poritidae dominate and preferred prey Acroporidae and Pocilloporidae are kept low by A. planci (Quinn and Kojis 2003). Alternatively, such changes may be temporary. Data taken from reefs in both Guam and Japan suggests that coral reefs may recover (in terms of species richness, density and fish assemblages) from starfish damage in as little as 10 to 20 years (Colgan 1987; Sano 2000). Colgan (1987) commented that the rapid recovery of a coral community from natural disturbance by A. planci demonstrates that some reef ecosystems have a greater resilience than once estimated. On the other hand, evidence to the contrary exists which is both alarming and disheartening. A study by Seymour and Bradbury (1999) showed that the average reef recovery time on the Great Barrier Reef (Australia) is lengthening over time, and it is harder for reefs to recover from recent outbreaks of A. planci than it has been in the past. The authors believe this indicates that key features of reef community structure have been damaged over time. Lourey Ryan and Miller (2000) found that for coral cover in areas of the Great Barrier Reef damaged by A. planci to increase by 30%, it would take an estimated 5 years to 1000+ years. This highlights the variability of rate recovery times between reefs and raises the possibility that not all reefs will recover from sustained outbreaks of A. planci (Lourey, Ryan and Miller 2000).

The possible implications of ongoing outbreaks of A. planci are alarming. However what makes the scenario even more alarming is that, throughout its range, coral reefs are coming under increasing pressure from human impacts. A recent report (Wilkinson 2004) predicts that 24% of the world’s reefs are under imminent risk of collapse through human pressures; and a further 26% are under longer term threat of collapse. Human impacts exacerbate the effects of natural disturbance such as A. planci outbreaks by contributing to coral mortality and reducing a reef’s ability to recover. For example, large-scale silt depositions contribute to reef degradation in the Indian Ocean, where disease, predation and stress are listed as the key factors in causing coral mortality (Ravindran, Raghukumar and Raghukumar 1999). Similarly, the degradation of coral reefs in Oman was found to be due to both natural and human causes, with damage from fishery activities being recorded as the most common human impact (Al-Jufaili 2005). Other human impacts to coral ecosystems in the area include coastal construction, recreational activities, oil pollution and eutrophication (causing nuisance algal growth) (Al-Jufaili 2005). Predation of corals by A. planci, storm damage, coral diseases and temperature-related stresses were the most commonly recorded natural impacts to coral reefs in the country (Al-Jufaili 2005). In the Cocos Island (off the coast of Costa Rica) coral reefs, already significantly damaged by the 1982-83 El Nino event, became further degraded by high densities of the corallivores A. planci and Arothron meleagris (the Guinea fowl pufferfish) and the bio-eroding Diadema mexicanum (the Mexican Pacific sea urchin) (Guzman and Cortes 1992). Surveys from 1987 found that in some areas of the reef live coral cover was as low as 3% and scientists believe the coral reefs of the Cocos Islands will need a time-frame in the order of centuries to recover their original reef-framework and thickness (Guzman and Cortes 1992). While human impacts on coral reefs can be mitigated relatively easily by reducing human impacts on the reef ecosystem, it is difficult to predict outbreaks of A. planci starfish and harder still to manage their populations once they have reached significant proportions.

Destruction of living coral reef ecosystems is a potential economic disaster for small isles and atolls of Oceania. Most inhabitants of the region derive almost all their protein from marine resources. The destruction of reefs would result in the destruction of fisheries, as well as increasing land erosion along the coast (Chesher 1969). Crown-of-thorns starfish outbreaks have hindered traditional fishing in Samoa (Birkeland and Lucus 1990) and elsewhere and dying coral reefs have put livelihoods in jeopardy. Tour boat operations, diving expeditions, eco-tourism and other tourist attractions based on reef environments are all at risk of economic loss due damage caused by the crown-of-thorns starfish. Popular tourist destinations in the Great Barrier Reef have been significantly degraded by A. planci. On Grub Reef, for example, live coral remaining after an outbreak was so poor that tour boat operators had to cease tours to the site altogether (Birkeland and Lucus 1990). Such potential outcomes have prompted control teams in Palau to engage other stakeholders in control efforts, approaching dive shops and tour operators to "adopt a reef" (Quarterly Report 2002), a control-management strategy which should be encouraged on a wider scale.

Many factors impact on the size and extent of A. planci outbreaks. The exact causes of outbreaks have not been determined with any certainty and may in fact vary depending on local and regional factors. Currently there are considered to be two main hypotheses for the anthropogenic causes of outbreaks. The first of these is the predator removal hypothesis. According to this view decreased post settlement mortality by the removal of predators such as fish and the shellfish (i.e. the giant triton) allows adult starfish to persist and build up in numbers on a reef. For instance some studies have shown that predation is an important determinant of survival rates of juvenile starfish (Keesing et al. 1996). In Mauritius high A. planci numbers have been linked to low numbers of its main predator, the mollusc Charonia tritonis (Triton’s trumpet). In Egypt removal of fish in the families Lethrinidae, Balistidae and Tetraododontidae have been linked to outbreaks of the crown-of-thorns starfish (Ormond et al. 1990, in PERSGA/GEF 2003). The second anthropogenic theory is the nutrient enrichment hypothesis. This revolves around increased pre-settlement survivorship of larval crown-of-thorns starfish. In this scenario terrestrial runoff due to extreme rainfall events or eutrophication causes nutrient enrichment of coastal waters. The increase in nutrients results in an increase in phytoplankton, upon which the starfish larvae feed, thereby increases their survival in the water column. Because starfish produce such a vast quantity of eggs even a small increase in survivorship leads to larger settlement of larvae onto a reef, which in turn leads to an outbreak. This mechanism has been implicated in outbreaks in Micronesia and Polynesia (Birkeland 1982). Similarly, frequent A. planci outbreaks on the Great Barrier Reef have been linked to increased nutrient delivery from the land (Brodie et al. 2005). River-promoted eutrophication (algal growth) is a significant factor in the demise of fringing reefs in the inner Great Barrier Reef lagoon and recorded levels of nano plankton growth in some regions are sufficient to promote the survival of A. planci larvae and may be implicated to starfish outbreaks (Bell 1992).

Finally it is worth noting that A. planci is not only a physical danger to corals. The crown-of-thorns starfish (as its name may suggest) has an array of penetrating spines which can produce a painful wound, as well as redness, swelling, vomiting, numbness and paralysis in humans. In at least one case, A. planci triggered a very nasty inflammatory response in a patient, which resulted in local swelling of the hand and fingers. Even following effective drug treatment the movement of the fingers was still limited six months later (Adler Kaul and Jawad 2002).

 

Risk and Impact Factors

Top of page Impact outcomes
  • Ecosystem change/ habitat alteration
  • Negatively impacts human health
  • Negatively impacts livelihoods
  • Negatively impacts tourism
  • Reduced native biodiversity
  • Threat to/ loss of native species
Impact mechanisms
  • Causes allergic responses
  • Predation

Uses

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During Acanthaster planci outbreaks in Japan, the carcasses of starfish were used as fertiliser (M. Yamaguchi, pers. comm., in Birkeland and Lucus 1990). It has also been suggested that A. planci can be successfully used for animal feed and may have potential as a viable alternative to fish feed. (Luo Peng et al. 2011). Acanthaster planci is a significant coral predator and is known as a keystone species. It has the potential to alter coral ecosystems in significant and important ways. This makes it a useful indicator species and one which should be monitored when assessing the health of coral reef ecosystems (see Hill and Wilkinson 2004).

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.

There is substantial research and information on both ecological and management-based aspects of the crown-of-thorns starfish (Acanthaster planci) and its control. A. planci has been recently discovered to be a species complex (see ‘Description’) but it is unclear whether this finding has implications for future management, in terms of a possible need for species-specific management (Vogler et al. 2008).

Management Information

Original text compiled by IUCN SSC Invasive Species Specialist Group (ISSG)
 

It is important to first determine whether the starfish population is at normal levels or can be considered to be outbreaking. "Normal" densities of A. planci are considered to be in the range of between 1 and 15 per hectare, depending on the amount of coral cover available. It is not recommended that the starfish be controlled when occurring at this level, as damage to corals can be sustained with no obvious long-term damage when the starfish occur at low densities (Lassig, 1995). The difference between "normal" and outbreaking populations should be obvious, often involving up to a 10-fold increase in starfish numbers. The policy of the Great Barrier Reef Marine Park Authority is that control of A. planci should be limited to small-scale measures in areas important to tourism or science, unless it can be proven that the outbreak was caused or exacerbated by human activity (Lassig, 1995).

The Great Barrier Reef Marine Protection Authority recommend that any control programmes be carried out at a realistic scale (up to 2-4 ha), have adequate funding, and be initiated as soon as possible after the outbreak has been detected. Control programmes are rarely one-off operations, with starfish often moving into the cleared areas, hence it is necessary for there to be a long-term commitment to the programme (Lassig, 1995).

Control programs in Micronesia and the Great Barrier Reef have involved the killing of up to 350 000 individual starfish, but in many cases it is believed that the population of A. planci would have decreased in size anyway without a control program (Birkeland and Lucus 1990). Approximately 15 million starfish have been killed in control programs throughout the last 15 years in the Indo-Pacific region (Moran, 1997). By far the largest of these programs was undertaken in the Ryukyu Islands (Japan) where almost 13 million starfish were removed from the reefs in that region (Moran 1997). Despite this intensive Japanese effort (costing approximately A$6 million) the control program was regarded to have been unsuccessful in either eradicating the crown-of-thorns starfish or preventing further coral mortality. One of the greatest obstacles to any control project for A. planci has been the delay to initiate control before significant damage to coral ecosystems has occurred (Birkeland and Lucus 1990). Arranging volunteers, bad weather and funding availability can all delay control commencement (Birkeland and Lucus 1990). Research into accurate predictions of when and where A. planci outbreaks will occur are essential to improve future control and increase the chances of success (Birkeland and Lucus 1990). For example, a hydrodynamics study found that due to the interaction of tidal, gravity and wind flows, some areas within the reef retained higher numbers of larvae than others. Surveillance of these locations, which may be correlated with initial recruitment of A. planci, could provide an 'early warning' strategy for monitoring and controlling future outbreaks of this starfish on reefs (Black and Moran 1991).

In general there is substantial research and information on both ecological and management-based aspects of the crown-of-thorns starfish and its control. For example, since late 1985 the Australian Federal Government has provided about $A2.5 million for research; the Australian Institute of Marine Science and the Great Barrier Reef Marine Park Authority have also supported the effort (Moran 1997). As of 1997, about 70 scientists throughout Australia were collaborating on about 58 different projects. Topics of research include: larval dispersal, developing monoclonal antibodies for A. planci to identify them from other starfish larvae in samples, determining coral reef and fish recovery rates after outbreaks, use of satellite photography to investigate the effects of starfish outbreaks, developing mathematical models to understand starfish outbreaks, determining the efficacy of starfish control, investigating potential biological control options, undertaking a risk analysis of the starfish and investigating starfish predation (Moran 1997). Recently, an Australian team demonstrated the first successful induction of a transmissible disease in A. planci using injection of thiosulfate-citrate-bile-sucrose agar (TCBS) culture medium into the starfish; this technique has potential to be used in a biocontrol programme. (Rivera-Posada et al. 2011)

Research is not limited to Australia, however. Recently, scientists from Japan have identified a feeding attractant for this starfish derived from the viscera of the sea urchin (Toxopneustes pileolus). Arrachidonic acid and alpha-linolenic acid (both unsaturated fatty acids) are found to have biological activity and it is anticipated that these attractants could be used to control A. planci (Teruya et al. 2001).

The best general management policy according to the Palau Conservation Society (1999) is not to interfere with outbreaks unless the areas are small and of special value such as a tourist or heritage site. Visual searches for starfish infestations using speed boats are a useful tool for locating A. planci aggregations (Crown of thorns starfish clean-up 2002). Hand-harvesting is the only widespread method used to date and is only feasible for protecting small areas - large scale control is not known (Birkeland and Lucus 1990). An estimated 1% of starfish will regenerate from fragments, which means cutting the starfish and dumping them back on the reef is a viable control option (Birkeland and Lucus 1990). This method is better than using chemicals, which foul the reef and are potentially harmful to humans (Birkeland and Lucus 1990). Alternatively the starfish may be removed from the reef and disposed of by dumping on land; however, this removes nutrients from the reef ecosystem and increases soil salinity at dumping sites (Birkeland and Lucus 1990). Chemical treatment of starfish with lethal compounds eliminates the disposal problem and is more efficient, with 100+ starfish injected per person per hour (Birkeland and Lucus 1990). The following toxins have been used successfully for killing the crown-of-thorns starfish: sodium bisulphate (Palau Conservation Society 1999), 25ml concentrated formalin, 15ml concentrated ammonia, 10ml 16% hydrochloric acid (HCl) and 10ml saturated copper sulphate (CuSO4) (Birkeland and Lucus 1990). Copper sulfate is the cheapest option, however, it is known to be toxic to some marine animals and there is concern about its unwanted effects on the coral-reef ecosystem (Birkeland and Lucus 1990). Harriott et al. (2003) and Lassig (1995) recommend sodium bisulfate as the safest and most effective toxin, although it is extremely costly.

Control teams may consist of bounty collectors, volunteers and/or employed control teams. As the spines of this starfish are poisonous care should be taken when reef walking (Moran 1997). Bounties are usually at the rate of $US.10 to $.20 per starfish, while the costs for employing a control team is significantly higher (Birkeland and Lucus 1990). For example, the bounty system was used in the Ryukyus, Japan, and cost 0.18 per starfish, whereas a control team used at Shikoku, Japan, cost $US16.29 per starfish (Birkeland and Lucus 1990). Bounty systems have also been used with success in American Samoa and Palau, but have failed in Guam, Saipan, Tinian and Rota - probably due to the inaccessibility of the areas of starfish infestation (Birkeland and Lucus 1990). Starfish need to be accessible to snorkellers and waders and there needs to be easy access to the site by car if the bounty system is to work (Birkeland and Lucus 1990). Sites that need to be accessed by scuba diving or other specialised means will not be suitable (Birkeland and Lucus 1990). Another limitation of the bounty method is that bounty hunters tend to focus on making a profit rather than controlling the starfish so they move from one dense aggregation to another leaving behind them a thin dispersal of starfish released from the competitive pressures of other starfish (Birkeland and Lucus 1990). A possible solution to this would be to combine the efforts of both bounty hunters with a control team whose job it would be to scour the area afterwards picking up the individual starfish which the bounty hunters had missed. An alternative option would be to educate the hunters on the importance of collecting, if possible, every last individual from a site in order to reduce future damage to coral colonies. Thirdly, the initial bounty price could be increased for the few remaining individuals at a site to encourage bounty hunters to collect them.

The effect of increased run-off from human terrestrial systems into rivers and then into the sea and associated reef ecosystems has been implicated with eutrophication (algal growth) (Brodie et al. 2005; Bell 1992). This could well be a principal causative factor of crown-of-thorns starfish outbreaks (Bell 1992). Therefore, in areas of the Great Barrier Reef where elevated levels of nutrients and algal growth exist, special precautions need to be exercised in the control of sewage effluents and run-off in the vicinity of coral reefs (Bell 1992). Such management policies should be applied elsewhere in the world where fragile coral systems exist.

Lastly, the removal by humans of large predators from marine systems through fishing activity may directly or indirectly (through trophic cascades) contribute towards A. planci outbreaks, though the causal link is unsubstantiated. Nevertheless, Sweatman (2008) showed that no-take zones in the Great Barrier Reef were less frequently affected by outbreaks of crown-of-thorns starfish than were unprotected zones. This suggests a role for marine protected areas (MPAs) in preventing A. planci outbreaks.

Harriott et al. (2003) discuss three current theories as to what causes A. planci outbreaks. They are: (1) Population fluctuations are a natural phenomenon, (2) Removal of natural predators of the starfish has allowed populations to expand, and (3) Human factors such as increased nutrient run-off (mentioned above) have caused an increase in the planktonic food available to the starfish larvae, hence increased numbers of adult starfish. Fraser et al. (2000) provide a guide to best management practices in the control of A. planci.

 

Bibliography

Top of page

Adler, M., Kaul, A.and Jawad, A.S.M. 2002. Foreign body synovitis induced by a crown-of-thorns starfish, Rheumatology 41: 230-231.

Al-Jufaili, S., Al-Jabri, M., Al-Baluchi, A., Baldwin, R.M., Wilson, S.C., West, F. and Matthews, A.D. 1999. Human impacts on coral reefs in the Sultanate of Oman, Estuarine Coastal & Shelf Science. 49(SUPPL. A): 65-74.

Babcock, R.C. and Mundy, C.N. 1992. Reproductive Biology, Spawning and Field Fertilization Rates of Acanthaster planci, Aust. J. Mar. Freshwater Res. 43: 525-534.

Babcock, R.C., Mundy, C.N. and Whitehead, D. 1994. Sperm diffusion models and in situ confirmation of long-distance fertilization in the free-spawning asteroid Acanthaster planci, Biological Bulletin (Woods Hole) 186 (1): 17-28.

Baker, V.J. and Coleman, G.J. 2000. A guide to the reef monitoring database: Long-term monitoring of the Great Barrier Reef. Townsville: Australian Institute of Marine Science

Bell, P.R.F. 1992. Eutrophication and coral reefs some examples in the Great Barrier Reef lagoon, Water Research 26 (5): 553-568.

Benzie, J.A.H. 1999. Major genetic differences between crown-of-thorns starfish (Acanthaster planci) populations in the Indian and Pacific Oceans, Evolution 53 (6): 1782-1795.

Birk, S. 1979. Crown of thorns Management Plan May 1979.

Birkeland, C. 1982. Terrestrial Runoff As a Cause of Outbreaks of Acanthaster planci (Echinodermata: Asteroidea), Marine Biology 69: 175-185

Birkeland, C. and Lucus, J.S. 1990. Acanthaster planci: major management problems of coral reefs. Florida: CRC Press.

Black, K.P. and Moran, P.J. 1991. Influence of hydrodynamics on the passive dispersal and initial recruitment of larvae of Acanthaster Planci Echinodermata Asteroidea on the Great Barrier Reef, Marine Ecology Progress Series 69 (1-2): 55-65.

Brodie, J., Fabricius, K., De'ath, G. and Okaji, K. 2005. Are increased nutrient inputs responsible for more outbreaks of crown-of-thorns starfish?, Marine Pollution Bulletin 51 (1-4): 266-278.

Brook, F.J. 1999. The coastal scleractinian coral fauna of the Kermadec Islands, southwestern Pacific Ocean, Journal of the Royal Society of New Zealand 29 (4): 435-460. http://www.rsnz.org/publish/jrsnz/1999/27.pdf

Cameron, A.M., Endean, R. and De Vantier, L.M. 1991. Predation on massive corals: Are devastating population outbreaks of Acanthaster-planci novel events?, Marine Ecology Progress Series 75 (2-3): 251-258.

Centre for Environment, Fisheries & Aquaculture Science (CEFAS)., 2008. Decision support tools-Identifying potentially invasive non-native marine and freshwater species: fish, invertebrates, amphibians. http://www.cefas.co.uk/projects/risks-and-impacts-of-non-native-species/decision-support-tools.aspx

Chesher, R.H. 1969. Destruction of Pacific corals by the sea star Acanthaster planci, Science 165: 280-283.

Chess, J.R., Hobson, E.S. and Howard, D.F. 1997. Interactions between Acanthaster planci (Echinodermata, Asteroidea) and Scleractinian Corals at Kona, Hawai'I, Pacific Science 51 (2): 121-133.

Colgan, M.W. 1987. Coral Reef Recovery on Guam (Micronesia) After Catastrophic Predation by Acanthaster planci, Ecology 68 (6): 1592-1605.

Crown of thorns starfish clean-up report: Light House Reef 7-03-2002. 2002.

De Vantier, L.M. and Deacon, G. 1990. Distribution of Acanthaster planci at Lord Howe Island Solomon Islands South Pacific Ocean the southernmost Indo-Pacific reef, Coral Reefs 9 (3): 145-148.

De'ath, G. and Moran, P.J. 1998. Factors affecting the behaviour of crown-of-thorns starfish (Acanthaster planci L.) on the Great Barrier Reef: 1: Patterns of activity, Journal of Experimental Marine Biology & Ecology 220 (1): 83-106.

Done, T.J. 1988. Simulation of recovery of pre-disturbance size in populations of Porites spp. damaged by the of thorns starfish Acanthaster planci, Marine Biology 100: 51-61.

Done, T.J., Dayton, P.K., Dayton, A.E., and Steger, R. 1991. Regional and local variability in recovery of shallow coral communities Moorea French Polynesia South Pacific Ocean and Central Great Barrier Reef Australia, Coral Reefs 9 (4): 183-192.

Fabricius, K.E. 1996. Ecosystem recovery after episodic disturbance: Resilience of some coral reefs after Acanthaster outbreaks, Senckenbergiana Maritima 27 (3-6): 227-235.

Fagoonee, I. 1990. Coastal marine ecosystems of Mauritius, Hydrobiologia 208: 55-62.

Faure, G. 1989. Degradation of coral reefs at Moorea Island French Polynesia by Acanthaster planci, Journal of Coastal Research 5 (2): 295-305.

Fraser, N., Crawford, B.R. and Kusen, J. 2000. Best practices guide for crown-of-thorns clean-ups. Proyek Pesisir Special Publication. Coastal Resources Center Coastal Management Report #2225. Coastal Resources Center, University of Rhode Island, Narragansett, Rhode Island. 38 pages.

Glynn, P.W. 1984. An amphinomid worm predator of the crown-of-thorns sea-star and general predation on asteroids in Eastern and Western Pacific coral reefs, Bulletin of Marine Science 35 (1): 54-71.

Glynn, P.W. 1993. Monsoonal upwelling and episodic Acanthaster predation as probable controls of coral reef distribution and community structure in Oman, Indian Ocean, Atoll Research Bulletin 0 (379): 1-66.

Guzman, H.M. and Cortes, J. 1989. Coral reef community structure at Cano Island Pacific Costa Rica, Marine Ecology 10 (1): 23-42.

Guzman, H.M. and Cortes, J. 1992. Cocos Island (Pacific of Costa Rica) coral reefs after the 1982-1983 El Nino disturbance, Revista de Biologia Tropical 40 (3): 309-324.

Harriott, V., Goggin, L. and Sweatman, H. 2003. Crown-of-thorns starfish on the Great Barrier Reef. Current state of knowledge. November 2003 (revised edition). CRC Reef Research Centre Ltd.

Hart, A.M. and Klumpp, D.W. 1996. Response of herbivorous fishes to crown-of-thorns starfish Acanthaster planci outbreaks: I. Substratum analysis and feeding ecology of Acanthurus nigrofuscus and Scarus frenatus, Marine Ecology Progress Series 132 (1-3): 11-19.

Hay, M.E., Parker, J.D., Burkepile, D.E., Caudill, C.C., Wilson, A.E., Hallinan, Z.P. and Chequer, A.D. 2004. Mutualisms and Aquatic Community Structure: The Enemy of My Enemy Is My Friend, Annu. Rev. Ecol. Evol. Syst. 35: 175–97.

Hill, J. and Wilkinson, C. 2004. Methods for Ecological Monitoring of Coral Reefs - A Resource for Managers.Townsville: Australian Institute of Marine Science.

Hoegh-Guldberg, O. 1994. Uptake of dissolved organic matter by larval stage of the crown-of-thorns starfish Acanthaster planci, Marine Biology (Berlin) 120 (1): 55-63.

Johnson, D.B., Moran, P.J. and Driml, S. 1990. Evaluation of a crown-of-thorns starfish Acanthaster planci control Program at Grub Reef Central Great Barrier Reef Australia, Coral Reefs 9 (3): 167-171.

Johnson, L.G. and Cartwright, C.M. 1996. Thyroxine-accelerated larval development in the crown-of-thorns starfish, Acanthaster planci, Biological Bulletin (Woods Hole) 190 (3): 299-301.

Keesing J.K. and Lucas J.S. 1992. Field measurement of feeding and movement rates of the crown-of-thorns starfish Acanthaster Planci, Journal of Experimental Marine Biology & Ecology 156 (1): 89-104.

Keesing J.K., Bradbury, R.H., Devantier, L.M., Riddle, M.J. and; De'ath, G. 1992. Geological evidence for recurring outbreaks of the crown-of-thorns starfish a reassessment from an ecological perspective, Coral Reefs 11 (2): 79-85.

Keesing, J.K., Wiedermeyer, W.L., Okaji, K., Halford, A.R., Hall, K.C. and Cartwright, C.M. 1996. Mortality rates of juvenile starfish Acanthaster planci and Nardoa spp. measured on the Great Barrier Reef, Australia and in Okinawa, Japan, Oceanologica Acta 19 (3-4): 441-448.

Lane, D.J.W. 1996. A crown-of-thorns outbreak in the eastern Indonesian Archipelago, February 1996. Coral Reefs. 15: 209-210.

Lassig, B. Controlling crown-of-thorns starfish. 1995. Great Barrier Reef Marine Park Authority.

Lourey, M.J., Ryan, D.A.J. and Miller, I.R. 2000. Rates of decline and recovery of coral cover on reefs impacted by, recovering from and unaffected by crown-of-thorns starfish Acanthaster planci: A regional perspective of the Great Barrier Reef, Marine Ecology Progress Series 196: 179-186.

Madl, P. 1998. Marine Biology I : Colloquial Meeting of Marine Biology I: Acanthaster planci. http://www.sbg.ac.at/ipk/avstudio/pierofun/planci/planci.htm

McKenna, S.A. and G.R. Allen (eds.). 2005. A Rapid Marine Biodiversity Assessment of the Coral Reefs of Northwest Madagascar, Bulletin of the Rapid Assessment Program 31, Conservation International, Washington, DC.

Moran, P. 1997. Crown-of-thorns starfish questions and answers. Australian Institute of Marine Science (AIMS). http://www.aims.gov.au/pages/reflib/cot-starfish/pages/cot-000.html

Nakamura, R. 1986. A morphometric study on Acanthaster planci populations in the Ryukyu Islands Japan, Galaxea 5 (2): 223-238.

Palau Conservation Society. 1999. Crown of thorns starfish control strategy draft.

PERSGA/GEF. 2003. Coral Reefs in the Red Sea and Gulf of Aden. Surveys 1990 to 2000 Summary and Recommendations. PERSGA Technical Series No. 7. PERSGA, Jeddah.

Pinca, S., Beger, M., Jacobson, D and Keju, T. Undated. The State of Coral Reef Ecosystems of the Marshall Islands

Pratchett, M.S. 2001. Influence of coral symbionts on feeding preferences of crown-of-thorns starfish Acanthaster planci in the western Pacific, Source Marine Ecology Progress Series 214: 111-119.

Quinn, N.J. and Kojis, B.L. 2003. The dynamics of coral reef community structure and recruitment patterns around Rota, Saipan, and Tinian, western Pacific, Bulletin of Marine Science 72 (3): 979-996.

Ravindran, J., Raghukumar, C. and Raghukumar, S. 1999. Disease and stress-induced mortality of corals in Indian reefs and observations on bleaching of corals in the Andamans, Current Science (Bangalore) 76 (2): 233-237.

Salvat, B., Hutchings, P., Aubanel, A., Tatarata, M. and Dauphin, C. Undated. The status of the coral reefs and marine resources of French Polynesia

Sano, M. 2000. Stability of reef fish assemblages: Responses to coral recovery after catastrophic predation by Acanthaster planci, Marine Ecology Progress Series 198: 121-130.

Seymour, R. M. 1989. Is Acanthaster planci a near-optimal predator?, Ecological Modelling 46 (3-4): 239-260.

Seymour, R.M. and Bradbury, R.H.1999. Lengthening reef recovery times from crown-of-thorns outbreaks signal systemic degradation of the Great Barrier Reef, Marine Ecology Progress Series. 176 (0): 1-10.

Sluka, R.D. and Miller, M.W. 1999. Status of crown-of-thorns starfish in Laamu Atoll, Republic of Maldives, Bulletin of Marine Science 65 (1): 253-258.

Teruya, T., Suenaga, K. Koyama, T., Nakano, Y. and Uemura, D. 2001. Arachidonic acid and alpha-linolenic acid, feeding attractants for the crown-of-thorns sea star Acanthaster planci, from the sea urchin Toxopneustes pileolus, Journal of Experimental Marine Biology & Ecology 266 (2): 123-134.

Tsuda, R.T. 1971. Status of Acanthaster planci and coral reefs in the Mariana and Caroline Islands June 1970 to May 1971. University of Guam.

Tsuda, R.T., Jones, R.S., Randall, R.H. and Struck, M.R. 1970. Acanthaster planci crown of thorns starfish: Resurvey of Saipan and Tinian: Survey of Aguijan. University of Guam.

Vicente, N. 1999. Natural treasures under heavy pressure Oceanorama 30: 7-12.

WWF. 2003. Fiji Islands marine ecoregion: An overview of outstanding biodiversity, threats, opportunities and key stakeholders for conservation.

References

Top of page

Appeltans W; Bouchet P; Boxshall GA; Broyer CDe; Voogd NJde; Gordon DP; Hoeksema BW; Horton T; Kennedy M; Mees J; Poore GCB; Read G; Stöhr S; Walter TC; Costello MJ, 2012. World Register of Marine Species. World Register of Marine Species. http://www.marinespecies.org

Bos AR, 2010. Crown-of-thorns outbreak at the Tubbataha reefs UNESCO World Heritage Site. Zoological Studies, 49(1):124. http://zoolstud.sinica.edu.tw/default.htm

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

Luo P; Hu C; Xia J; Ren C; Jiang X, 2011. Chemical constituent analysis of the crown-of-thorns starfish Acanthaster planci and potential utilization value of the starfish as feed ingredient for animals. African Journal of Biotechnology, 10:13610-13616.

Narváez K; Zapata FA, 2010. First record and impact of the crown-of-thorns starfish, Acanthaster planci (Spinulosida: Acanthasteridae) on corals of Malpelo Island, Colombian Pacific. Revista de Biología Tropical, 58:139-4.

Rivera-Posada JA; Pratchett M; Cano-Gómez A; Arango-Gómez JD; Owens L, 2011. Injection of Acanthaster planci with thiosulfate-citrate-bile-sucrose agar (TCBS). I. Disease induction. Diseases of Aquatic Organisms, 97(2):85-94. http://www.int-res.com/articles/dao_oa/d097p085.pdf

Sweatman H, 2008. No-take reserves protect coral reefs from predatory starfish. Current Biology, 18:R598-R599.

Timmers MA; Andrews KR; Bird CE; deMaintenton MJ; Brainard RE; Toonen RJ, 2011. Widespread Dispersal of the Crown-of-Thorns Sea Star, Acanthaster planci, across the Hawaiian Archipelago and Johnston Atoll. Journal of Marine Biology:Article ID 934269.

Vogler C; Benzie J; Lessios H; Barber P; Wörheide G, 2008. A threat to coral reefs multiplied? Four species of crown-of-thorns starfish. Biology Letters, 4(6):696-699. http://rsbl.royalsocietypublishing.org/content/4/6/696.full

Distribution References

Appeltans W, Bouchet P, Boxshall GA, Broyer CDe, Voogd NJde, Gordon DP, Hoeksema BW, Horton T, Kennedy M, Mees J, Poore GCB, Read G, Stöhr S, Walter TC, Costello MJ, 2012. World Register of Marine Species. In: World Register of Marine Species, http://www.marinespecies.org

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

Narváez K, Zapata FA, 2010. First record and impact of the crown-of-thorns starfish, Acanthaster planci (Spinulosida: Acanthasteridae) on corals of Malpelo Island, Colombian Pacific. In: Revista de Biología Tropical, 58 139-4.

Contributors

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    Reviewed by: Ian Miller, Coordinator of Broadscale Surveys AIMS Long Term Monitoring Program Australian Institute of Marine Science. Australia
    Compiled by: IUCN/SSC Invasive Species Specialist Group (ISSG) with support from La Fondation d'entreprise Total
 
    Last Modified: Tuesday, 9 January 2007

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