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RESEARCH ARTICLE

Discriminating populations of medusae (Chironex fleckeri, Cubozoa) using statolith microchemistry

Christopher J. Mooney A and Michael J. Kingsford A B
+ Author Affiliations
- Author Affiliations

A Marine Biology and Aquaculture, College of Science and Engineering and the ARC Centre of Excellence for Coral Reef Studies, James Cook University, Townsville, Qld 4811, Australia.

B Corresponding author. Email: michael.kingsford@jcu.edu.au

Marine and Freshwater Research 68(6) 1144-1152 https://doi.org/10.1071/MF16104
Submitted: 31 March 2016  Accepted: 19 August 2016   Published: 13 September 2016

Abstract

The structure of medusae populations is poorly known. Natural geochemical signatures based on elemental composition of calcified structures are a common tool for investigating population structure or connectivity in marine systems. Chironex fleckeri (Cubozoa) medusae have a hard calcified structure, the statolith. Laser ablation–inductively coupled plasma mass spectrometry was used to determine the elemental composition of statoliths at varying spatial scales. We investigated medusae population structure using both univariate (element : Ca ratios) and multivariate (multi-element : Ca signature) analyses. Significant differences in some elemental ratios were found among regions (separated by hundreds of kilometres) and among many sites (separated by kilometres) within regions. Canonical discriminant analyses of multi-element : Ca signatures successfully distinguished between both regions and sites within regions with correct classifications of 100% of samples to some locations. Statolith microchemistry can help discriminate populations of jellyfish, but a multiseason comparison demonstrated the need to calibrate spatial differences by season. Our evidence and recent ecological data suggest that populations of C. fleckeri medusae are highly localised at spatial scales of kilometres; potential causal factors are discussed.

Additional keywords: box jellyfish, laser ablation–inductively coupled plasma mass spectrometry, LA-ICP-MS, population substructure.


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