Free Standard AU & NZ Shipping For All Book Orders Over $80!
Register      Login
Marine and Freshwater Research Marine and Freshwater Research Society
Advances in the aquatic sciences
RESEARCH ARTICLE

Scale-dependent relationships between benthic habitat characteristics and abundances of blacklip abalone, Haliotis rubra (Leach)

Elisabeth M. A. Strain A B D and Craig R. Johnson A C
+ Author Affiliations
- Author Affiliations

A School of Zoology and TAFI, Private Bag 5, University of Tasmania, Hobart, Tasmania 7001, Australia.

B Present Address: Queen’s University, School of Biological Sciences, Medical Biology Centre, 97 Lisburn Road, Belfast, UK.

C Institute for Marine and Antarctic Studies, Private Bag 129, University of Tasmania, Hobart, Tasmania 7001, Australia.

D Corresponding author. Email: strain.beth@gmail.com

Marine and Freshwater Research 61(11) 1227-1236 https://doi.org/10.1071/MF09211
Submitted: 25 August 2009  Accepted: 19 May 2010   Published: 16 November 2010

Abstract

Habitat characteristics can influence marine herbivore densities at a range of spatial scales. We examined the relationship between benthic habitat characteristics and adult blacklip abalone (Haliotis rubra) densities across local scales (0.0625–16 m2), at 2 depths, 4 sites and 2 locations, in Tasmania, Australia. Biotic characteristics that were highly correlated with abalone densities included cover of non-calcareous encrusting red algae (NERA), non-geniculate coralline algae (NCA), a matrix of filamentous algae and sediment, sessile invertebrates, and foliose red algae. The precision of relationships varied with spatial scale. At smaller scales (0.0625–0.25 m2), there was a positive relationship between NERA and ERA, and negative relationships between sediment matrix, sessile invertebrates and abalone densities. At the largest scale (16 m2), there was a positive relationship between NERA and abalone densities. Thus, for some biotic characteristics, the relationship between NERA and abalone densities may be scalable. There was very little variability between depths and sites; however, the optimal spatial scale differed between locations. Our results suggest a dynamic interplay between the behavioural responses of H. rubra to microhabitat and/or to abalone maintaining NERA free of algae, sediment, and sessile invertebrates. This approach could be used to describe the relationship between habitat characteristics and species densities at the optimal spatial scales.

Keywords: correlation, H. rubra, percentage cover, quantile regression, scale-dependent.


Acknowledgements

We thank those who assisted with fieldwork, particularly Bob Connell, Michael Davis and Richard Holmes. This study was part of a PhD supported by an Australian Postgraduate Award. The research was supported by Tasmanian Aquaculture and Fisheries Institute and Tasmanian Abalone Council grants. The research was undertaken using the permits 5003, 5182 and 7038 issued by the Department of Environment and Primary Industries, Tasmania. We thank the editor Professor Andrew Boulton and two anonymous reviewers for their helpful comments on earlier versions of the manuscript.


References

Anderson, M. J. (2008). Animal–sediment relationships re-visited: characterising species’ distributions along an environmental gradient using canonical analysis and quantile regression splines. Journal of Experimental Marine Biology and Ecology 366, 16–27.
Crossref | GoogleScholarGoogle Scholar | Cohen J. (1998). ‘Statistical Power Analysis for Behavioural Sciences.’ (Hove and London: Hilldale, NJ, USA.)

Connell, S. D. (2003). The monopolization of understorey habitat by subtidal encrusting coralline algae: a test of combined effects of canopy-mediated light and sedimentation. Marine Biology 142, 1065–1071.
Nash W. J. (1995). The development of new techniques for assessing and managing the Australian abalone fisheries. Grant 88/94, Technical Report to the Fisheries Research and Development Corporation, Department of Primary Industries and Fisheries, Hobart, Tasmania.

Prince J. (1989). The fisheries biology of the Tasmanian stocks of Haliotis rubra. Ph.D. Thesis, University of Tasmania, Hobart.

R Development Core Team (2010). R: A Language and Environment for Statistical Computing (Version 2.8). Available at http://www.R-project.org

Shepherd, S. A. (1973). Studies on southern Australian abalone (genus Haliotis) I. Ecology of five sympatric species. Australian Journal of Marine and Freshwater Research 24, 217–257.
Crossref | GoogleScholarGoogle Scholar | Shepherd S. A., and Steinberg P. D. (1992). Food preferences of three abalone species with a review of the food of abalone. In ‘Abalone of The World: Biology, Fisheries and Culture’. (Eds S. A. Shepherd, M. J. Tegner and S. A. Guzman del Proo.) pp. 169–181. (Blackwell Scientific: Oxford.)

Shepherd, S. A. , and Turner, J. A. (1985). Studies on southern Australian abalone (genus Haliotis). 6. Habitat preferences, abundance and predators of juveniles. Journal of Experimental Marine Biology and Ecology 93, 285–298.
Crossref | GoogleScholarGoogle Scholar |

Steneck, R. S. (1982). A limpet coralline algae association: adaptations and defenses between a selection herbivore and its prey. Ecology 63, 507–522.
Crossref | GoogleScholarGoogle Scholar |

Syms, C. (1995). Multi-scale analysis of habitat association in a guild of blennioid fishes. Marine Ecology Progress Series 125, 31–43.
Crossref | GoogleScholarGoogle Scholar |

Valentine, J. P. , Tarbath, D. , Frusher, S. D. , Mundy, C. N. , and Buxton, C. D. (2010). Limited evidence for ecosystem-level change on reefs exposed to Haliotis rubra (‘blacklip abalone’) exploitation. Austral Ecology 35, 1–13.


Vaz, S. , Martin, C. S. , Eastwood, P. D. , Ernade, B. , and Carpentier, A. , et al. (2008). Modeling species distribution using regression quantiles. Journal of Applied Ecology 45, 204–217.
Crossref | GoogleScholarGoogle Scholar |