Salinity tolerance of riverine microinvertebrates from the southern Murray–Darling Basin
Ben J. Kefford A C , Elizabeth J. Fields A , Colin Clay A B and Dayanthi Nugegoda AA Biotechnology and Environmental Biology, School of Applied Sciences, RMIT University, PO Box 71, Bundoora, Vic. 3083, Australia.
B Current address: PO Box 192, Boronia, Vic. 3155, Australia.
C Corresponding author. Email: ben.kefford@rmit.edu.au
Marine and Freshwater Research 58(11) 1019-1031 https://doi.org/10.1071/MF06046
Submitted: 20 March 2006 Accepted: 5 October 2007 Published: 3 December 2007
Abstract
Concern about the effect of rising salinity on freshwater biodiversity has led to studies investigating the salt tolerance of macroinvertebrates and fish, with less attention given to microinvertebrates. We investigated the acute lethal effects of salinity on 12 microinvertebrate species from rivers in the southern Murray–Darling Basin in central Victoria, Australia. For a subset of these species, sub-lethal salinity effects and the effect of water temperature on salinity tolerance were also investigated. The most sensitive microinvertebrates had broadly similar 72-h LC50 values to the most sensitive macroinvertebrates, reported in other studies. However, the most tolerant microinvertebrates tested were much more sensitive than the most tolerant macroinvertebrates and the microinvertebrates studied were more sensitive than most freshwater fish. Temperature affected the acute lethal toxicity of salinity but only to a small degree. In three of four species (the exception being Hydra viridissima), the effects of salinity on growth, development and/or reproduction at concentrations below their 72-h LC50 values were observed. However, different endpoints responded differently to salinity. The demonstrated effect of salinity on microinvertebrates has the potential to indirectly affect fish and salt-tolerant macroinvertebrates via changes to their prey species or ecological functions performed by microinvertebrates.
Additional keywords: microcrustaceans, Newnhamia fenestra, salinisation, Simocephalus, zooplankton.
Acknowledgements
This work was funded by Land and Water Australia (LWA) and the Murray–Darling Basin Commission, as part of the National River Contaminants Program (LWA project no. RMI 12), and the Queensland Department of Natural Resources and Mines. Kefford is currently supported by an Australian Research Council Fellowship (LP0882481). Rob Walsh is thanked for checking and correcting the identification of specimens. We appreciate the time given by Satish Choy, Brendan Edgar, Leon Metzeling, Richard Marchant, Daryl Nielsen, Carolyn Palmer and Phil Papas through their attendance on a steering committee and informal discussions and comments on a draft by Liliana Zalizniak and Richard Marchant.
Aladin, N. V. , and Potts, W. T. W. (1995). Osmoregulatory capacity of the Cladocera. Journal of Comparative Physiology. B, Biochemical, Systemic, and Environmental Physiology 164, 671–683.
| Crossref | GoogleScholarGoogle Scholar |
Blinn, D. W. , Halse, S. A. , Pinder, A. M. , Shiel, R. J. , and McRae, J. M. (2004). Diatom and micro-invertebrate communities and environmental determinants in western Australian wheatbelt: a response to salinization. Hydrobiologia 528, 229–248.
| Crossref | GoogleScholarGoogle Scholar |
Forbes, V. E. , and Calow, P. (1999). Is the per capita rate of increase a good measure of population-level effects in ecotoxicology? Environmental Toxicology and Chemistry 18, 1544–1556.
| Crossref | GoogleScholarGoogle Scholar |
Nielsen, D. L. , Brock, M. , Crossle, K. , Harris, K. , Healey, M. , and Jarosinski, I. (2003a). The effects of salinity on aquatic plant germination and zooplankton hatching from two wetlands sediments. Freshwater Biology 48, 2214–2223.
| Crossref | GoogleScholarGoogle Scholar |
Nielsen, D. L. , Brock, M. A. , Rees, G. N. , and Baldwin, D. S. (2003b). The effects of increasing salinity on freshwater ecosystems in Australia. Australian Journal of Botany 51, 655–665.
| Crossref | GoogleScholarGoogle Scholar |
Pinder, A. M. , Halse, S. A. , McRae, J. M. , and Shiel, R. J. (2005). Occurrence of aquatic invertebrates of the wheatbelt region of Western Australia in relation to salinity. Hydrobiologia 543, 1–24.
| Crossref | GoogleScholarGoogle Scholar |
Pinder, A. M. , Halse, S. A. , Shiel, R. J. , Cale, D. J. , and McRae, J. M. (2002). Halophile aquatic invertebrates in the wheatbelt region of south-western Australia. Verhandlungender Internatnationalen Verelinigung für Theoretische und Angewandte Limnologie 28, 1687–1694.
Pollino, C. A. , and Holdway, D. A. (1999). Potential of two hydra species as standard toxicity test animals. Ecotoxicology and Environmental Safety 43, 309–316.
| Crossref | GoogleScholarGoogle Scholar | PubMed |
Radke, L. C. , Howard, K. W. F. , and Gell, P. A. (2002). Chemical diversity in south-eastern Australian saline lakes. I: geochemical causes. Marine and Freshwater Research 53, 941–959.
| Crossref | GoogleScholarGoogle Scholar |
Schallenberg, M. , and Burns, C. W. (2003). A temperate, tidal lake-wetland complex. 2. Water quality and implications for zooplankton community structure. New Zealand Journal of Marine and Freshwater Research 37, 429–447.
Schallenberg, M. , Hall, C. J. , and Burns, C. W. (2003). Consequences of climate-induced salinity increases on zooplankton abundance and diversity in coastal lakes. Marine Ecology Progress Series 251, 181–189.
| Crossref | GoogleScholarGoogle Scholar |
Skinner, R. , Sheldon, F. , and Walker, K. F. (2001). Propagules in dry weland sediments as indicators of ecological health: effects of salinity. Regulated Rivers: Research and Management 17, 191–197.
| Crossref | GoogleScholarGoogle Scholar |
Sunderam, R. M. , Patra, R. W. , Julli, M. , and Warne, M. St. J. (2004). Use of the up- and- down acute toxicity test procedure to generate LC50 data for fish. Bulletin of Environmental Contamination and Toxicology 72, 873–880.
| Crossref | GoogleScholarGoogle Scholar | PubMed |
Sutcliffe, D. W. (1974). Sodium regulation and adaptation to freshwater in the isopod genus Asellus. The Journal of Experimental Biology 61, 719–736.
| PubMed |
Williams, D. D. , Williams, N. E. , and Cao, Y. (2000). Road salt contamination of groundwater in a major metropolitan area and development of a biological index to monitor its impact. Water Research 34, 127–138.
| Crossref | GoogleScholarGoogle Scholar |
Williams, W. D. (1999). Salinisation: a major threat to water resources in the arid and semi-arid regions of the world. Lakes and Reservoirs: Research and Management 4, 85–91.
| Crossref | GoogleScholarGoogle Scholar |
Zalizniak, L. , Kefford, B. J. , and Nugegoda, D. (2006). Is all salinity the same? I The effect of ionic proportions on the salinity tolerance of five species of freshwater invertebrates. Marine and Freshwater Research 57, 75–82.
| Crossref | GoogleScholarGoogle Scholar |
Zalizniak, L. , Kefford, B. J. , and Nugegoda, D. (in press a). Effects of different ionic compositions on survival and growth of Physa acuta. Aquatic Ecology. ,
| Crossref | GoogleScholarGoogle Scholar |
Zalizniak, L. , Kefford, B. J. , and Nugegoda, D. (in press b). Effects of pH on salinity tolerance of selected freshwater invertebrates. Aquatic Ecology. ,
| Crossref | GoogleScholarGoogle Scholar |