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Australian Journal of Zoology Australian Journal of Zoology Society
Evolutionary, molecular and comparative zoology
RESEARCH ARTICLE

Range decline and conservation status of Westralunio carteri Iredale, 1934 (Bivalvia : Hyriidae) from south-western Australia

Michael W. Klunzinger A B D , Stephen J. Beatty A , David L. Morgan A , Adrian M. Pinder C and Alan J. Lymbery A
+ Author Affiliations
- Author Affiliations

A Freshwater Fish Group and Fish Health Unit, Centre for Fish and Fisheries Research, School of Veterinary and Life Sciences, Murdoch University, Murdoch, WA 6150, Australia.

B Malacology Section, Department of Aquatic Zoology, Collections and Research Facility, Western Australian Museum, Welshpool, WA 6160, Australia.

C Science and Conservation Division, Department of Parks and Wildlife, Kensington, WA 6151, Australia.

D Corresponding author. Email: m.klunzinger@murdoch.edu.au

Australian Journal of Zoology 63(2) 127-135 https://doi.org/10.1071/ZO15002
Submitted: 5 January 2015  Accepted: 21 April 2015   Published: 12 May 2015

Abstract

Westralunio carteri is the only species of freshwater mussel found in south-western Australia and, owing to a lack of comprehensive information on its ecology, its conservation status has been speculative. To more accurately predict the true conservation status of this species, the historical and contemporary distributional records were modelled with environmental data that identified salinity, perenniality and total nitrogen as variables responsible for limiting the species’ current extent of occurrence, inferring threatening processes. The species was found to have undergone a 49% reduction in extent of occurrence in less than three generations, due primarily to secondary salinisation. Current distribution is bounded by Gingin Brook in the north to the Kent, Goodga and Waychinicup Rivers in the South, within 50–100 km of coastal south-western Australia. Field observations indicated that W. carteri was almost never found at sites where mean salinity was >1.6 g L–1. This was corroborated by laboratory tolerance trials that showed that W. carteri has an acute salinity tolerance (LD50) of 1.6–3.0 g L–1. Application of IUCN Red List criteria indicates that W. carteri qualifies for listing as vulnerable. Conservation management measures should focus on maintaining existing populations.

Additional keywords: freshwater mussel, salinity, species distribution model, threatened species.


References

Aldridge, D. C., Fayle, T. M., and Jackson, N. (2007). Freshwater mussel abundance predicts biodiversity in UK lowland rivers. Aquatic Conservation: Marine and Freshwater Ecosystems 17, 554–564.
Freshwater mussel abundance predicts biodiversity in UK lowland rivers.Crossref | GoogleScholarGoogle Scholar |

AWRC (1976). ‘Review of Australia’s Water Resources 1975’. (Australian Water Resources Council (AWRC), Department of Natural Resources: Canberra.)

Bartoñ, K. (2013). ‘MuMIn: Multi-model Inference. Version 1.9.5’. Available at: http://cran.r-project.org/web/packages/MuMIn [Accessed on 01 September 2013].

Beatty, S. J., Morgan, D. L., Rashnavadi, M., and Lymbery, A. J. (2011). Salinity tolerances of endemic freshwater fishes of south-western Australia: implications for conservation in a biodiversity hotspot. Marine and Freshwater Research 62, 91–100.
Salinity tolerances of endemic freshwater fishes of south-western Australia: implications for conservation in a biodiversity hotspot.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BC3MXmtFGlsg%3D%3D&md5=2c683c0dabbcd679cd9df47f8b853d1dCAS |

Bogan, A. E., and Roe, K. J. (2008). Freshwater bivalve (Unioniformes) diversity, systematics, and evolution: status and future directions. Journal of the North American Benthological Society 27, 349–369.
Freshwater bivalve (Unioniformes) diversity, systematics, and evolution: status and future directions.Crossref | GoogleScholarGoogle Scholar |

Brainwood, M. A., Klunzinger, M. W., and Walker, K. F. (2014). Now you see them, soon you won’t—freshwater mussel conservation in Australia. Australian Society for Fish Biology and Australian Society of Limnology Congress, 30 June – 4 July, 2014, Darwin, Northern Territory, Australia. (Abstract #13410).

Burnham, K. P., and Anderson, D. R. (2002). ‘Model Selection and Multi-Model Inference: A Practical Information-Theoretic Approach’. (Springer: New Jersey.)

Cañedo-Argüelles, M., Kefford, B. J., Piscart, C., Prat, N., Schäfer, R. B., and Schulz, C. J. (2013). Salinisation of rivers: An urgent ecological issue. Environmental Pollution 173, 157–167.
Salinisation of rivers: An urgent ecological issue.Crossref | GoogleScholarGoogle Scholar | 23202646PubMed |

Cardoso, P., Borges, P. A. V., Triantis, K. A., Ferrández, M. A., and Martín, J. L. (2012). The underrepresentation and misrepresentation of invertebrates in the IUCN Red List. Biological Conservation 149, 147–148.
The underrepresentation and misrepresentation of invertebrates in the IUCN Red List.Crossref | GoogleScholarGoogle Scholar |

Dormann, C. F., McPherson, J. M., Araújo, M. B., Bivand, R., Bolliger, J., Carl, G., Davies, R. G., Hirzel, A., Jetz, W., Kissling, W. D., Kühn, I., Ohlemüller, R., Peres-Neto, P. R., Reineking, B., Schröder, B., Schurr, F. M., and Wilson, R. (2007). Methods to account for spatial autocorrelation in the analysis of distributional species data: A review. Ecography 30, 609–628.
Methods to account for spatial autocorrelation in the analysis of distributional species data: A review.Crossref | GoogleScholarGoogle Scholar |

Elith, J., and Leathwick, J. (2009). Species distribution models: Ecological explanation and prediction across space and time. Annual Review of Ecology, Evolution and Systematics 40, 677–697.
Species distribution models: Ecological explanation and prediction across space and time.Crossref | GoogleScholarGoogle Scholar |

Freckleton, R. P. (2011). Dealing with collinearity in behavioural and ecological data: model averaging and the problems of measurement error. Behavioral Ecology and Sociobiology 65, 91–101.
Dealing with collinearity in behavioural and ecological data: model averaging and the problems of measurement error.Crossref | GoogleScholarGoogle Scholar |

Geoscience Australia (2003). ‘GEODATA TOPO 250K, Series 2’. (National Mapping Division, Commonwealth of Australia Department of Industry, Tourism and Resources: Canberra.)

Graf, D. L. (2013). Patterns of freshwater bivalve global diversity and the state of phylogenetic studies on the Unionoida, Sphaeriidae, and Cyrenidae. American Malacological Bulletin 31, 135–153.
Patterns of freshwater bivalve global diversity and the state of phylogenetic studies on the Unionoida, Sphaeriidae, and Cyrenidae.Crossref | GoogleScholarGoogle Scholar |

Graf, D. L., Jones, H., Geneva, A. J., Pfeiffer, J. M., and Klunzinger, M. W. (2015). Molecular phylogenetic analysis supports a Gondwanan origin of the Hyriidae (Mollusca: Bivalvia: Unionida) and the paraphyly of Australasian taxa. Molecular Phylogenetics and Evolution 85, 1–9.
Molecular phylogenetic analysis supports a Gondwanan origin of the Hyriidae (Mollusca: Bivalvia: Unionida) and the paraphyly of Australasian taxa.Crossref | GoogleScholarGoogle Scholar | 25659337PubMed |

Haag, W. R. (2013). ‘North American Freshwater Mussels: Natural History, Ecology and Conservation.’ (Cambridge University Press: New York.)

Halse, S. A., Ruprecht, J., and Pinder, A. M. (2003). Salinisation and prospects for biodiversity in rivers and wetlands of south-west Western Australia. Australian Journal of Botany 51, 673–688.
Salinisation and prospects for biodiversity in rivers and wetlands of south-west Western Australia.Crossref | GoogleScholarGoogle Scholar |

Heiberger, R. M. (2013). ‘HH: Statistical Analysis and Data Display. Version 2.3–37.’ Available at: http://cran.r-project.org/web/packages/HH/ [accessed 01 September 2013].

Hortal, J., Jiménez-Valverde, J., Goméz, J. F., Lobo, J. M., and Baselga, A. (2008). Historical bias in biodiversity inventories affects the observed environmental niche of the species. Oikos 117, 847–858.
Historical bias in biodiversity inventories affects the observed environmental niche of the species.Crossref | GoogleScholarGoogle Scholar |

Iredale, T. (1934). The freshwater mussels of Australia. Type species: Westralunio ambiguus carteri. Australian Zoologist 8, 57–78.

IUCN (1996). Mollusc Specialist Group 1996. Westralunio carteri. In ‘International Union for the Conservation of Nature Red List of Threatened Species. Version 2.3’. Available at: http://www.iucnredlist.org. [accessed 01 June 2009].

IUCN (2013). ‘Guidelines for using the IUCN Red List categories and criteria. Version 10’. Available at: http://www.iucnredlist.org/documents/RedListGuidelines.pdf. [accessed 01 May 2013].

Jones, H. A., and Byrne, M. (2014). Changes in the distributions of freshwater mussels (Unionoida: Hyriidae) in coastal south-eastern Australia and implications for their conservation status. Aquatic Conservation: Marine and Freshwater Ecosystems 24, 203–217.
Changes in the distributions of freshwater mussels (Unionoida: Hyriidae) in coastal south-eastern Australia and implications for their conservation status.Crossref | GoogleScholarGoogle Scholar |

Kelly, G. E. (2001). The median lethal dose – design and estimation. The Statistician 50, 41–50.
The median lethal dose – design and estimation.Crossref | GoogleScholarGoogle Scholar |

Kendrick, G. W. (1976). The Avon: faunal and other notes on a dying river in south-western Australia. Western Australian Naturalist (Perth) 13, 97–114.

Klunzinger, M., and Walker, K. F. (2014). Westralunio carteri. In ‘IUCN Red List of Threatened Species. Version 2014.3’. Available at: www.iucnredlist.org. [accessed 21 December 2014].

Klunzinger, M. W., Beatty, S. J., Morgan, D. L., Thomson, G. J., and Lymbery, A. J. (2012a). Glochidia ecology in wild fish populations and laboratory determination of competent host fishes for an endemic freshwater mussel of south-western Australia. Australian Journal of Zoology 60, 26–36.
Glochidia ecology in wild fish populations and laboratory determination of competent host fishes for an endemic freshwater mussel of south-western Australia.Crossref | GoogleScholarGoogle Scholar |

Klunzinger, M. W., Beatty, S. J., Morgan, D. L., Lymbery, A. J., Pinder, A. M., and Cale, D. J. (2012b). Distribution of Westralunio carteri Iredale 1934 (Bivalvia: Unionoida: Hyriidae) on the south coast of southwestern Australia, including new records of the species. Journal of the Royal Society of Western Australia 95, 77–81.

Klunzinger, M. W., Thomson, G. J., Beatty, S. J., Morgan, D. L., and Lymbery, A. J. (2013). Morphological and morphometrical description of the glochidia of Westralunio carteri Iredale, 1934 (Bivalvia: Unionoida: Hyriidae). Molluscan Research 33, 104–109.
Morphological and morphometrical description of the glochidia of Westralunio carteri Iredale, 1934 (Bivalvia: Unionoida: Hyriidae).Crossref | GoogleScholarGoogle Scholar |

Klunzinger, M. W., Beatty, S. J., Morgan, D. L., Lymbery, A. J., and Haag, W. R. (2014). Age and growth in the Australian freshwater mussel, Westralunio carteri, with an evaluation of the fluorochrome calcein for validating the assumption of annulus formation. Freshwater Science 33, 1127–1135.
Age and growth in the Australian freshwater mussel, Westralunio carteri, with an evaluation of the fluorochrome calcein for validating the assumption of annulus formation.Crossref | GoogleScholarGoogle Scholar |

Köhler, F. (2011). Westralunio carteri. In ‘IUCN Red List of Threatened Species. Version 2011.2’. Available at: http://www.iucnredlist.org. [accessed 03 February 2012].

Lamoreux, J., Akçakaya, H. R., Bennun, L., Collar, N. J., Boitani, L., Brackett, D., Brautigam, A., Brooks, T. M., da Fonseca, G. A. B., Mittermeier, R. A., Rylands, A. B., Gärdenfors, U., Hilton-Taylor, C., Mace, G., Stein, B. A., and Stuart, S. (2003). Value of the IUCN Red List. Trends in Ecology & Evolution 18, 214–215.
Value of the IUCN Red List.Crossref | GoogleScholarGoogle Scholar |

Leathwick, J. R., Rowe, D., Richardson, J., Elith, J., and Hastie, T. (2005). Using multivariate adaptive regression splines to predict the distributions of New Zealand’s freshwater diadromous fish. Freshwater Biology 50, 2034–2052.
Using multivariate adaptive regression splines to predict the distributions of New Zealand’s freshwater diadromous fish.Crossref | GoogleScholarGoogle Scholar |

Lopes-Lima, M., Teixiera, A., Froufe, E., Lopes, A., Varandas, S., and Sousa, R. (2014). Biology and conservation of freshwater bivalves: past, present and future perspectives. Hydrobiologia 735, 1–13.
Biology and conservation of freshwater bivalves: past, present and future perspectives.Crossref | GoogleScholarGoogle Scholar |

Mayer, X., Ruprecht, J., and Bari, M. (2005). Stream salinity status and trends in southwest Western Australia. Salinity and Land Use Impacts. SLUI 38. Department of Environment, Perth.

McMichael, D. F., and Hiscock, I. D. (1958). A monograph of the freshwater mussels (Mollusca: Pelecypoda) of the Australian region. Australian Journal of Marine and Freshwater Research 9, 372–507.
A monograph of the freshwater mussels (Mollusca: Pelecypoda) of the Australian region.Crossref | GoogleScholarGoogle Scholar |

Montgomery, D. C., and Peck, E. A. (1992). ‘Introduction to Linear Regression Analysis. ’ 2nd edn. (John Wiley & Sons: New York.)

Morgan, D. L., Thorburn, D. C., and Gill, H. S. (2003). Salinization of southwestern Western Australian rivers and the implications for the inland fish fauna – the Blackwood River, a case study. Pacific Conservation Biology 9, 161–171.

Murdoch University and SERCUL (2010). ‘Mussel Watch Western Australia.’ Archived by PANDORA, Australia’s Web Archive. National Library of Australia and Partners. Available at: http://nla.gov.au/nla.arc-131363. [archived 13 January 2012].

Murray, K., and Connor, M. M. (2009). Methods to quantify variable importance: implications for the analysis of noisy ecological data. Ecology 90, 348–355.
Methods to quantify variable importance: implications for the analysis of noisy ecological data.Crossref | GoogleScholarGoogle Scholar | 19323218PubMed |

Myers, R. (1990). ‘Classical and Modern Regression with Applications.’ (Duxbury: Boston.)

Newton, A. C. (2010). Use of a Bayesian network for Red Listing under uncertainty. Environmental Modelling & Software 25, 15–23.
Use of a Bayesian network for Red Listing under uncertainty.Crossref | GoogleScholarGoogle Scholar |

NLWRA (2001). Australian Dryland Salinity Assessment 2000: extent, impacts, processes, monitoring and management options. National Land and Water Resources Audit (NLWRA), Canberra.

Partridge, G. J., Lymbery, A. J., and George, R. J. (2008). Finfish mariculture in inland Australia: a review of potential water sources, species and production platforms. Journal of the World Aquaculture Society 39, 291–310.
Finfish mariculture in inland Australia: a review of potential water sources, species and production platforms.Crossref | GoogleScholarGoogle Scholar |

Pen, L. J. (1999). ‘Managing our Rivers. A Guide to the Nature and Management of the Streams of South-West Western Australia.’ (Water and Rivers Commission: East Perth.)

Pinder, A. M., Halse, S. A., McRae, J. M., and Shiel, R. J. (2004). Aquatic invertebrate assemblages of wetlands and rivers in the wheat belt region of Western Australia. Records of the Western Australian Museum, , 7–37.

Playford, T. J., and Walker, K. F. (2008). Status of the endangered Glenelg River mussel Hyridella glenelgensis (Unionoida: Hyriidae) in Australia. Aquatic Conservation: Marine and Freshwater Ecosystems 18, 679–691.
Status of the endangered Glenelg River mussel Hyridella glenelgensis (Unionoida: Hyriidae) in Australia.Crossref | GoogleScholarGoogle Scholar |

R Development Core Team (2013). ‘R: A Language and Environment for Statistical Computing. Version 3.0.1’. (R Foundation for Statistical Computing: Vienna.)

Rodrigues, A. S. L., Pilgrim, J. D., Lamoreux, J. F., Hoffmann, M., and Brooks, T. M. (2006). The value of the IUCN Red List for conservation. Trends in Ecology & Evolution 21, 71–76.
The value of the IUCN Red List for conservation.Crossref | GoogleScholarGoogle Scholar |

Seddon, M., Darwall, M., Bohn, M., Allen, D., and Smith, K. (2012). Update on the status of the Global Freshwater Mollusc Assessment. In ‘International Meeting on Biology and Conservation of Freshwater Bivalves: Book of Abstracts’. (Eds A. Teixiera, M. Lopes-Lima, S. Varandas, R. Sousa, E. Froufe and F. Teiga.) p. 30. (School of Agriculture, Polytechnic Institute of Bragança: Bragança, Portugal.)

Smith, T. G. (1996). The water quality and invertebrate fauna of the Avon River: a highly saline but productive aquatic ecosystem. B.Sc.(Honours) Thesis, Murdoch University, Perth.

Spooner, D. E., and Vaughn, C. C. (2006). Context‐dependent effects of freshwater mussels on stream benthic communities. Freshwater Biology 51, 1016–1024.
Context‐dependent effects of freshwater mussels on stream benthic communities.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD28XmvVymsrw%3D&md5=4b06e9b42fe5cf9f98f55c7205ebd92cCAS |

State of Western Australia (2014). Division 6 – Molluscs: 169. Westralunio carteri – Carter’s Freshwater Mussel. In ‘Wildlife Conservation (Specially Protected Fauna) Notice 2014 – Schedule 1 – Fauna that is Rare or is Likely to Become Extinct’. p. 4477. Government Gazette, WA: 2 December, 2014: No. 188. State Law Publisher of Western Australia, Perth.

Walker, K. F. 1981. ‘Ecology of Freshwater Mussels in the River Murray.’ (Australian Water Resources Council: Canberra.)

Walker, K. F., Byrne, M., Hickey, C. W., and Roper, D. S. (2001). Freshwater mussels (Hyriidae) of Australasia. In ‘Ecology and Evolution of the Freshwater Mussels Unionoida’. (Eds G. Bauer and K. Wächtler.) pp. 5–31. (Springer: Berlin.)

Walker, K. F., Jones, H. A., and Klunzinger, M. W. (2014). Bivalves in a bottleneck: taxonomy, phylogeography and conservation of freshwater mussels (Bivalvia: Unionoida) in Australasia. Hydrobiologia 735, 61–79.
Bivalves in a bottleneck: taxonomy, phylogeography and conservation of freshwater mussels (Bivalvia: Unionoida) in Australasia.Crossref | GoogleScholarGoogle Scholar |

White, W. T., Hall, N. G., and Potter, I. C. (2002). Size and age compositions and reproductive biology of the nervous shark Carcharhinus cautus in a large subtropical embayment, including an analysis of growth during pre- and postnatal life. Marine Biology 141, 1153–1164.
Size and age compositions and reproductive biology of the nervous shark Carcharhinus cautus in a large subtropical embayment, including an analysis of growth during pre- and postnatal life.Crossref | GoogleScholarGoogle Scholar |

Williams, W. D. (2001). Anthropogenic salinisation of inland waters. Hydrobiologia 466, 329–337.
Anthropogenic salinisation of inland waters.Crossref | GoogleScholarGoogle Scholar |

Williams, W. D., Taaffe, R. G., and Boulton, A. J. (1991). Longitudinal distribution of macroinvertebrates in two rivers subject to salinisation. Hydrobiologia 210, 151–160.
Longitudinal distribution of macroinvertebrates in two rivers subject to salinisation.Crossref | GoogleScholarGoogle Scholar |

Wintle, B. A., Elith, J., and Potts, J. M. (2005). Fauna habitat modelling and mapping: a review and case study in the Lower Hunter Central Coast region of NSW. Austral Ecology 30, 719–738.
Fauna habitat modelling and mapping: a review and case study in the Lower Hunter Central Coast region of NSW.Crossref | GoogleScholarGoogle Scholar |