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Environmental Science and Pollution Research

, Volume 26, Issue 2, pp 1576–1583 | Cite as

Toxic effect and physiological disruption of sodium phosphate to the quagga mussel (Dreissena bugensis)

  • Kannappan VijayavelEmail author
  • Donna R. Kashian
Research Article
  • 33 Downloads

Abstract

Phosphorous is an essential nutrient for all forms of life; however, the question of toxicity to aquatic species remains largely unanswered, despite many systems that exceed natural phosphorus loads. This study determined the ecotoxicological threshold concentration of phosphorus to the freshwater bivalve Dreissena bugensis using a 96-h bioassay. Sublethal, medial lethal, and lethal levels of sodium phosphate to D. bugensis were found to be 125, 260, and 476 ppm. Physiological biomarkers such as the oxygen consumption and filtration rate were estimated by exposing D. bugensis to five different sublethal concentrations (25, 50, 75, 100, and 125 ppm) of sodium phosphate for 96 h. Both oxygen consumption and filtration rate gradually declined with increasing exposure concentrations and durations, which was significant (α < 0.05) for 75, 100, and 125 ppm of sodium phosphate concentrations. Based on the feeding rate and oxygen consumption endpoints, the no-observed effect concentration and the low observed effect concentration were 25 and 75 ppm, respectively. Maximum acceptable toxicant concentration of sodium phosphate was 43.3 ppm. Measured environmental concentration (MEC) of total phosphorus (0.015 ppm; n = 6) was obtained from seasonal field assessments in Saginaw Bay during the years 2008 to 2010. An assessment factor of 1000 was used for calculating the predicted no effect concentration (PNEC) of 0.025 ppm. Risk quotient (RQ) of “0.6” was therefore established using MEC/PNEC (real risk) ratio. Binary ecological classification (RQ < 1) suggested that there is no appreciable risk of phosphorus to D. bungensis in the Saginaw Bay of Lake Huron of Laurentian Great Lakes.

Keywords

Acute toxicity Sublethal stress Quagga mussel Phosphorus Bio-indicator 

Notes

Acknowledgements

We thank Hunter Oates, Sander Robinson, and Brittanie Dabney for their valuable help during mussel collection and laboratory assays.

Funding information

This research was sponsored by the National Oceanic and Atmospheric Administration Center for Sponsored Coastal Ocean Research and Wayne State University.

References

  1. Alexander JE Jr, Thorp JH, Fell RD (1994) Turbidity and temperature effects on oxygen consumption in the zebra mussel (Dreissena polymorpha). Can J Fish Aquat Sci 51:179–184CrossRefGoogle Scholar
  2. Bentley RE, Dean JW, Hollister TA, LeBlanc GA, Sauter A, Sleight BH, Wilson WG (1978) “Laboratory evaluation of the toxicity of elemental phosphorus (P4) to aquatic organisms”; U.S. Army Med. Res. Dev. Command, Washington, D.C.:105 p. (U.S. NTIS AD-A061785)Google Scholar
  3. Berg DJ, Fisher SW, Landrum PF (1996) Clearance and processing of algal particles by Zebra mussels (Dressiena). J Great Lakes Res 22(3):779–788CrossRefGoogle Scholar
  4. Chapman PM, Fairbrother A, Brown D (1998) A critical evaluation of safety (uncertainty) factors for ecological risk assessment. Environ Toxicol Chem 17:99–108CrossRefGoogle Scholar
  5. Chen LH, Yang JL (2007) Acute toxicity of antimony chloride (SbCl3) and its effects on oxygen consumption of common carp (Cyprinus carpio). Bull Environ Contam Toxicol 78:459–462CrossRefGoogle Scholar
  6. Chinni S, Khan RN, Yallapragada PR (2000) Oxygen consumption, ammonia-N-excretion and metal accumulation in Penaeus indicus post larvae exposed to lead. Bull Environ Contam Toxicol 64:144–151CrossRefGoogle Scholar
  7. Connon RE, Geist J, Werner I (2012) Effect-based tools for monitoring and predicting the ecotoxicological effects of chemicals in the aquatic environment. Sensors 12:12741–12771CrossRefGoogle Scholar
  8. De Lafontaine Y, Gagne F, Blaise C, Costan G, Gagnon P, Chan HM (2000) Biomarkers in zebra mussels (Dreissena polymorpha) for the assessment and monitoring of water quality of the St. Lawrence River (Canada). Aquat Toxicol 50:51–71CrossRefGoogle Scholar
  9. Effler SW, Boone SR, Siegfried C, Ashby SL (1998) Dynamics of zebra mussel oxygen demand in Seneca River, New York. Environ Sci Technol 32:807–812CrossRefGoogle Scholar
  10. Eggen RIL, Behra R, Burkhardt-Holm P, Escher BI, Schweigert N (2004) Challenges in ecotoxicology. Environ Sci Technol 38:58–64CrossRefGoogle Scholar
  11. Fanslow DL, Nalepa TF, Lang GA (1995) Filtration rates of the Zebra mussels (Dressena polymorpha) on the natural seston from Saginaw Bay, Lake Huron. J Great Lakes Res 21(4):489–500CrossRefGoogle Scholar
  12. Grobler E, Vanvuren JHJ, Du Preez HH (1989) Routine oxygen consumption of Tilapia sparrmanii (Cichlidae) following acute exposure to atrazine. Comp Biochem Physiol C 93(1):37–42CrossRefGoogle Scholar
  13. Hartmann JT, Beggel S, Auerswald K, Stoeckle BC, Geist J (2016) Establishing mussel behavior as a biomarker in ecotoxicology. Aquat Toxicol 170:279–288CrossRefGoogle Scholar
  14. International Joint Commission (1988) Great Lakes Water Quality Agreement (GLWQA) of 1978 as amended by Protocol signed November 18: 1987Google Scholar
  15. Karan V, Vitorvic S, Tutundzic V, Poleksic V (1998) Functional enzymes activity and gill histology of carp after copper sulfate exposure and recovery. Ecotoxicol Environ Saf 40:49–55CrossRefGoogle Scholar
  16. Kim E, Yoo S, Ro H, Han HJ, Baek YW, Eom IC, Kim HM, Kim P, Choi K (2013) Aquatic toxicity assessment of phosphate compounds. Environ Health Toxicol 28:1–7Google Scholar
  17. Lin P, Klump JV, Guo L (2016) Dynamics of dissolved and particulate phosphorus influenced by seasonal hypoxia in Green Bay, Lake Michigan. Sci Total Environ 541:1070–1082CrossRefGoogle Scholar
  18. Marvin CH, McCarry BE, Bryant DW (1994) Determination and genotoxicity of polycyclic aromatic hydrocarbons isolated from Dreissina polymorpha (zebra mussels) sampled from Hamilton Harbour. J Great Lakes Res 20:523–530CrossRefGoogle Scholar
  19. Nowicki CJ, Kashian DR, Van Heese E (2014) Comparative effects of sediment versus aqueous PCB exposure on benthic and planktonic invertebrates. Environ Toxicol Chem 33:641–647CrossRefGoogle Scholar
  20. Patel B, Anthony K (1991) Uptake of cadmium in tropical marine lamellibranchs, and effects on physiological behavior. Mar Biol 108:457–470CrossRefGoogle Scholar
  21. Rainbow PS, Wolowicz M, Fialkowski W, Smith BD, Sokolowski A (2000) Biomonitoring of trace metals in the gulf of Gdansk, using mussels (Mytilus trossulus) and barnacles (Balanus improvisus). Water Res 34:1823–1829CrossRefGoogle Scholar
  22. Richman LA, Somers K (2005) Can we use zebra and quagga mussels for biomonitoring contaminants in the Niagara River? Water Air Soil Pollut 167:155–178CrossRefGoogle Scholar
  23. Rutzke MA, Gutenmann WH, Lisk DJ, Mills EL (2000) Toxic and nutrient element concentrations in soft tissues of zebra and quagga mussels from lakes Erie and Ontario. Chemosphere 40:1353–1356CrossRefGoogle Scholar
  24. Stow CA, Dyble J, Kashian DR, Johengen TH, Winslow KP, Peacor SD, Mille D (2014) Phosphorus targets and eutrophication objectives in Saginaw Bay: a 35-year assessment. J Great Lakes Res 40:4–10CrossRefGoogle Scholar
  25. Sze PWC, Lee SY (2000) Effects of chronic copper exposure on the green mussel Perna viridis. Mar Biol 137(3):379–392CrossRefGoogle Scholar
  26. The Lake Huron Binational Partnership (2006) Phosphorus in Saginaw Bay have we met the target? Fact Sheet:1–4Google Scholar
  27. U.S. Environmental Protection Agency (1992) Probit analysis program used for calculating LC/EC values version 1.5. Ecological Monitoring. Research Division. Environmental Monitoring System Laboratory, CincinnatiGoogle Scholar
  28. Vijayavel K, Balasubramanian MP (2006) Changes in oxygen consumption and respiratory enzymes as stress indicators in an estuarine edible crab Scylla serrata exposed to naphthalene. Chemosphere 63(9):1523–1531CrossRefGoogle Scholar
  29. Vijayavel K, Balasubramanian MP (2007) Interaction of potash and decis on the ecophysiology of a fresh water fish Oreochromis mossambicus. Ecotoxicol Environ Saf 66(2):154–158CrossRefGoogle Scholar
  30. Watenpaugh DE, Beitinger TL (1985) Oxygen consumption in fathead minnows Pimephales bpromelas following acute exposure to water borne selenium. Comp Biochem Physiol C 80:253–256CrossRefGoogle Scholar
  31. Watling HR, Watling RJ (1982) Comparative effects of metals on the filtering rate of the brown mussel (Perna perna). Bull Environ Contam Toxicol 29:651–657CrossRefGoogle Scholar

Copyright information

© Springer-Verlag GmbH Germany, part of Springer Nature 2018

Authors and Affiliations

  1. 1.Department of Biological SciencesWayne State UniversityDetroitUSA

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