Abstract
Outbreaks of coral predators are defined as increases (often rapid) in their abundance above threshold densities that can be sustained by local coral assemblages, which in turn depends on the abundance and turnover of coral prey. To investigate the outbreak densities of the corallivorous gastropod Drupella cornus, we conducted both in situ feeding and coral growth experiments at Mandu reef within the Ningaloo Marine Park, Western Australia. Over two 10-day periods, we tagged and photographed feeding scars on colonies of the tabulate coral Acropora spicifera that harboured Drupella feeding aggregations. We calculated a mean in situ Drupella consumption rate of 1.16 ± 1.1 cm2 coral area individual−1 d−1. We also determined coral growth rates by tagging and photographing 24 colonies of Acropora spicifera at time zero and then again 1 year later. We calculated a mean linear extension rate of 7.9 ± 3.7 cm yr−1 for actively growing Acropora spicifera, which we then used to estimate A. spicifera growth rates over a range of coral cover values. This combination allowed us to determine the maximum number of Drupella that could be sustained across a range of coral cover. Our data suggest that the outbreak density of Drupella at the average level of coral cover for back reef sites at Mandu reef (17.6 ± 13.7%) is approximately 0.95 individuals m−2 reef area. At the maximum coral cover observed at Mandu reef (60%), the outbreak density of Drupella is estimated to be approximately 2.83 individuals m−2 reef area. Establishing Drupella outbreak densities assists managers in predicting possible outbreak abundances and in monitoring coral reef health.
Similar content being viewed by others
References
Al-Horani FA, Hamdi M, Al-Rousan SA (2011) Prey selection and feeding rates of Drupella cornus (Gastropoda: Muricidae) on corals from the Jordanian Coast of the Gulf of Aqaba, Red Sea. Jordan J Biol Sci 4:191–198
Al-Moghrabi SM (1997) Bathymetric distribution of Drupella cornus and Coralliophila neritoidea in the Gulf of Aqaba (Jordan). Proceedings of the 8th International Coral Reef Symposium, 2:1345-1350
Antonius A, Riegl B (1997) A possible link between coral diseases and a corallivorous snail (Drupella cornus) outbreak in the Red Sea. Atoll Res Bull 447:1–9
Armstrong SJ (2009) Ningaloo Marine Park Drupella long-term monitoring program: data collected during the 2008 survey. Marine Science Program Data Report Series: MSPDR5. Department of Environment and Conservation, Western Australia
Ayling AM, Ayling AL (1987) Ningaloo Marine Park: preliminary fish density assessment and habitat survey, with information on coral damage due to Drupella grazing. Report to the Department of Conservation and Land Management, Western Australia
Ayling AM (2000) The effects of Drupella spp. grazing on coral reefs in Australia. Sea Research, http://www.searesearch.com.au/reports/drupella/drupella.html
Babcock RC, Plagányi ÉE, Morello EB, Rochester W (2014). What are the important thresholds and relationships to inform the management of COTS? Final Report, 30 June 2014. CSIRO, Australia
Babcock RC, Dambacher JM, Morello EB, Plagányi ÉE, Hayes KR, Sweatman HPA, Pratchett MS (2016) Assessing different causes of crown-of-thorns starfish outbreaks and appropriate responses for management on the Great Barrier Reef. PLOS One 11(12):e0169048
Baums IB, Miller MW, Szmant AM (2003) Ecology of a corallivorous gastropod, Coralliophila abbreviata, on two scleractinian hosts. II. Feeding, respiration and growth. Mar Biol 142:1093–1101
Black R, Johnson MS (1994) Growth rates in outbreak populations of the corallivorous gastropod Drupella cornus (Roding 1798) at Ningaloo Reef, Western Australia. Coral Reefs 13:145–150
Boucher L (1986) Coral predation by muricid gastropods of the genus Drupella at Enewetak, Marshall Islands. Bull Mar Sci 38:9–11
Bruckner AW, Coward G, Bimson K, Rattanawongwan T (2017) Predation by feeding aggregations of Drupella spp. inhibits the recovery of reefs damaged by a mass bleaching event. Coral Reefs 36:1181–1187
Bruckner RJ, Bruckner AW, Williams EH Jr (1997) Life history strategies of Coralliophila abbreviata Lamarck (Gastropoda:Coralliophilidae) on the southeast coast of Puerto Rico. Proc 8th Int Coral Reef Sym 1:627–632
Cassata L, Collins LB (2008) Coral reef communities, habitats and substrates in and near sanctuary zones of Ningaloo Marine Park. J Coast Res 24:139–151
Claremont M, Reid DG, Williams ST (2011) Evolution of corallivory in the gastropod genus Drupella. Coral Reefs 30:977–990
Cumming RL (1999) Predation on reef-building corals: multiscale variation in the density of three corallivorous gastropods, Drupella spp. Coral Reefs 18:147–157
Cumming RL (2009a) Population outbreaks and large aggregations of Drupella on the Great Barrier Reef. Great Barrier Reef Marine Park Authority, Research Publication 96, Townsville, Australia
Cumming RL (2009b) Case study: impact of Drupella spp. on reef-building corals of the Great Barrier Reef. Great Barrier Reef Marine Park Authority, Research Publication 97, Townsville, Australia
Drury C, Manzello D, Lirman D (2017) Genotype and local environment dynamically influence growth, disturbance response and survivorship in the threatened coral, Acropora cervicornis. PLoS ONE 12:e0174000
English S, Wilkinson C, Baker V (1997) Survey manual for tropical marine resources. Australian Institute of Marine Science, Townsville
Forde MJ (1992) Populations, behaviour and effects of Drupella cornus on the Ningaloo Reef, Western Australia. Department of Conservation and Land Management (CALM), CALM Occasional Paper 3/92, Western Australia
Fujioka Y, Yamazato K (1983) Host selection of some Okinawan coral associated gastropods belonging to the genera Drupella, Coralliophila and Quoyula. Galaxea 2:59–73
Hoeksema BW, Scott C, True JD (2013) Dietary shift in corallivorous Drupella snails following a major bleaching event at Koh Tao, Gulf of Thailand. Coral Reefs 32:423–428
Jonker MM, Johns KK, Osborne KK (2008) Surveys of benthic reef communities using underwater digital photography and counts of juvenile corals. Long-term Monitoring of the Great Barrier Reef. Standard Operational Procedure Number 10/2008. Australian Institute of Marine Science (AIMS)
Keesing JK, Lucas JS (1992) Field measurement of feeding and movement rates of the crown-of-thorns starfish Acanthaster planci (L.). J Exp Mar Bio Ecol 156:89–104
Kita M, Kitamura M, Tomoyuki K, Teruya T, Matsumoto H, Nakano Y, Uemura D (2005) Feeding attractants for the muricid gastropod Drupella cornus, a coral predator. Tetrahedron Lett 46:8583–8585
Kohn AJ (1961) Chemoreception in gastropod molluscs. Am Zool 1:291–308
Madin JS, Baird AH, Dornelas M, Connolly SR (2014) Mechanical vulnerability explains size dependent mortality of reef corals. Ecol Lett 17:1008–1015
Madin JS, Connolly SR (2006) Ecological consequences of major hydrodynamic disturbances on coral reefs. Nature 444:477–480
Moerland MS, Scott CM, Hoeksema BW (2016) Prey selection of corallivorous muricids at Koh Tao (Gulf of Thailand) four years after a major coral bleaching event. Contrib Zool 85:291–309
Moran PJ, De’ath G (1992) Estimates of the abundance of the crown-of-thorns starfish Acanthaster planci in outbreaking and non-outbreaking populations on reefs within the Great Barrier Reef. Mar Biol 113:509–515
Morton B, Blackmore G, Kwok CT (2002) Corallivory and prey choice by Drupella rugosa (Gastropoda: Muricidae) on Honk Kong. J Molluscan Stud 68:217–223
Moyer JT, Emerson WK, Ross M (1982) Massive destruction of scleractinian corals by the muricid gastropod, Drupella, in Japan and the Philippines. The Nautilus 96:69–82
Pratchett MS, Anderson KD, Hoogenboom MO, Widman E, Baird AH, Pandolfi JM, Edmunds PJ, Lough JM (2015) Spatial, temporal and taxonomic variation in coral growth—implications for the structure and function of coral reef ecosystems. Oceanogr Mar Biol 53:215–295
Pratchett M, Caballes C, Rivera-Posada J, Sweatman H (2014) Limits to understanding and managing outbreaks of crown-of-thorns starfish (Acanthaster spp.). Oceanogr Mar Biol Ann Rev 52:133–200
R Development Core Team (2011) R: A language and environment for statistical computing. www.R-project.org/ (accessed 1 January 2017)
Robertson R (1970) Review of the predators and parasites of stony corals, with special reference to symbiotic prosobranch gastropods. Pac Sci 24:43–54
Schneider CA, Rasband WS, Eliceiri KW (2012) NIH Image to ImageJ: 25 years of image analysis. Nat Methods 102:671
Schoepf V, Herler J, Zuschin M (2010) Microhabitat use and prey selection of the coral-feeding snail Drupella cornus in the northern Red Sea. Hydrobiologia 641:45–57
Shafir S, Gur O (2008) A Drupella cornus outbreak in the northern Gulf of Eilat and changes in coral prey. Coral Reefs 27:379
Shaver EC, Shantz AA, McMinds R, Burkepile DE, Thurber RLV, Silliman BR (2017) Effects of predation and nutrient enrichment on the success and microbiome of a foundational coral. Ecology 98:830–839
Simpson C (1988) Ecology of Scleractinian corals in the Dampier Archipelago, Western Australia. Technical Report No.23, Environmental Protection Authority, Western Australia
Speed CW, Babcock RC, Bancroft KP, Beckley LE, Bellchambers LM, Depczynski M, Field SN, Friedman KJ, Gilmour JP, Hobbs JPA, Kobryn HT, Moore JAY, Nutt CD, Shedrawi G, Thomson DP, Wilson SK (2013) Dynamic stability of coral reefs on the West Australian coast. PLoS ONE 8(7):e69863
Stimson J (1996) Wave-like outward growth of some table- and plate-forming corals, and a hypothetical mechanism. Bull Mar Sci 58:301–313
Turner SJ (1994) The biology and population outbreaks of the corallivorous gastropod Drupella on Indo-Pacific reefs. Oceanogr Mar Biol 32:461–530
Veron JEN (1986) Corals of Australia and the Indo-Pacific. Angus and Robertson, London, Sydney
Acknowledgements
This work was funded by the Gorgon Barrow Island Net Conservation Benefits Fund, which was administered by the WA Department of Parks and Wildlife. The work was conducted under the following permits: Department of Parks and Wildlife Regulation 17 and 4; #01-000096-1, SF010543, SF010083, SF010082, and CE005047, CE004661, CE004685; and Department of Fisheries Exemption 2418. We thank Mark Wilson and Ben Kelly for their logistical support. We also thank John Keesing, three anonymous reviewers, the handling editor, and the editor, Morgan Pratchett, for providing valuable suggestions to the manuscript.
Author information
Authors and Affiliations
Corresponding author
Ethics declarations
Conflicts of interest
The authors declare no conflicts of interest.
Additional information
Topic Editor Morgan S. Pratchett
Rights and permissions
About this article
Cite this article
Bessey, C., Babcock, R.C., Thomson, D.P. et al. Outbreak densities of the coral predator Drupella in relation to in situ Acropora growth rates on Ningaloo Reef, Western Australia. Coral Reefs 37, 985–993 (2018). https://doi.org/10.1007/s00338-018-01748-7
Received:
Accepted:
Published:
Issue Date:
DOI: https://doi.org/10.1007/s00338-018-01748-7