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Quantifying larvae of the coralivorous seastar Acanthaster cf. solaris on the Great Barrier Reef using qPCR

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dc.contributor Australian Inst Marine Sci
dc.contributor Australian Institute Of Marine Science UTHICKE, SVEN DOYLE, JASON R. MCKINNON, A. DAVID 2017-11-19T18:09:08Z 2017-11-19T18:09:08Z 2017-11-19T18:09:08Z 2017-11-19T18:09:08Z 2017-08-01
dc.identifier.citation Doyle JR, McKinnon AD, Uthicke S (2017) Quantifying larvae of the coralivorous seastar Acanthaster cf. solaris on the Great Barrier Reef using qPCR. Marine Biology 164: 176
dc.identifier.issn 0025-3162
dc.description.abstract Coral reefs are under threat from a variety of sources including the corallivorous seastar, Acanthaster cf. solaris. (Crown of Thorns Seastar; CoTS). Outbreak prediction is a strategic component of managing the impact of this boom and bust species. Details on the fate and dispersal of planktonic life stages are limited, with CoTS larval stages indistinct morphologically from many other asteroid larvae. Given the similarity of many larvae, quantification of marine larvae stages is a major challenge for marine ecologists. We describe a quantitative polymerase chain reaction (qPCR) assay that enables the enumeration of CoTS larvae in field collected plankton samples. Specific primers for the mitochondrial cytochrome oxidase subunit 1 gene (mtCOI) were developed and validated for specificity and sensitivity. Larval culture experiments with CoTS allowed us to determine the mtCOI copy number per larval stage which aided in relating copy numbers in the plankton to actual larval densities. We found the mtCOI copy number varied 3.6-fold across all CoTS planktonic life stages from unfertilised oocyte to competent brachiolaria and this variation was taken into account when determining CoTS larval densities in field samples on the Great Barrier Reef (GBR). CoTS larvae were detected at many locations in the CoTS 'initiation box' on the GBR between Cairns and Lizard Island in December 2014 with the highest mean CoTS larval density at 36.9 ( 23.7-84.3) CoTS larvae m(3) between Rudder and Tongue Reef (16.233 degrees S, 145.643 degrees E). Field negative samples taken outside spawning season along with DNA extraction recovery experiments confirmed our sampling, extraction and assay methods were robust. This method will greatly help further studies on understanding CoTS larval ecology and outbreaks, with methods developed also important tools for other ecologically and commercially important marine species.
dc.description.sponsorship The authors wish to thank Professor Gert Worheide of the Luwig Maximilians University, Germany for the generous donation of CoTS tissue from non-GBR locations. We are grateful to Association of Marine Park Tourism Operators for ongoing support in field sampling and provision of experimental animals. We would also like to extend our gratitude to the crew of the RV Cape Ferguson and staff from the National Sea Simulator (SeaSim) for their continuing support in marine research at AIMS. Funding for this research was provided by the Australian Institute of Marine Science and the Great Barrier Reef Marine Park Authority.
dc.language English
dc.subject Plankton
dc.subject Gene Flow
dc.subject Outbreaks
dc.subject Planci L.
dc.subject Echinodermata
dc.subject Plankton Samples
dc.subject Quantification
dc.subject Quantitative Pcr
dc.subject Environmental Dna
dc.subject Species-specific Detection
dc.subject Real-time Pcr
dc.subject Of-thorns Starfish
dc.subject Marine & Freshwater Biology
dc.title Quantifying larvae of the coralivorous seastar Acanthaster cf. solaris on the Great Barrier Reef using qPCR
dc.type journal article
dc.identifier.doi 10.1007/s00227-017-3206-x
dc.identifier.wos WOS:000410485700004

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