Skip to main content
Log in

Trace elements in Anadara spp. (Mollusca: Bivalva) collected along the coast of Vietnam, with emphasis on regional differences and human health risk assessment

  • Original Article
  • Environment
  • Published:
Fisheries Science Aims and scope Submit manuscript

Abstract

This study measured concentrations of 21 trace elements in whole soft tissue of the blood cockle Anadara spp., which is a common food for local people, collected along the coast of Vietnam. Results showed that concentrations of As, Sr, Mo, Sn, and Pb in cockles collected from Khanh Hoa Province in the Central Coastal Zone (CCZ) had higher values than those from the other regions, while cockles collected from the Mekong River Delta (MRD) showed the highest concentrations of Hg. Regional differences in trace element concentrations of the cockle may be due to differences in human activities, i.e., shipyards in the CCZ and agriculture in the MRD. Trace element concentrations measured in the soft tissues of blood cockles investigated here were within safe levels for human consumption following criteria by the European Commission (EC) and the United States Food and Drug Agency, but several specimens had Cd levels exceeding the EC guidelines of 1 μg/g wet weight. The estimated target hazard quotients for trace elements via consuming bivalves were <1, indicating that the cumulative noncarcinogenic risk was completely insignificant. However, the estimated target cancer risk values by assumed inorganic As concentrations seem to implicate consumption of these cockles as posing potential human health concerns.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Fig. 1
Fig. 2
Fig. 3
Fig. 4
Fig. 5
Fig. 6

Similar content being viewed by others

References

  1. MONRE (Vietnamese Ministry of Natural Resources and Environment) (2004) Country report on land based pollution in Vietnam 2004. MONRE, Hanoi

  2. MOFI (Vietnamese Ministry of Fisheries) (2006) Guidelines for environmental management of aquaculture investments in Vietnam. MOFI, Hanoi

  3. Huang H, Wu JY, Wu JH (2007) Heavy metal monitoring using bivalved shellfish from Zhejiang Coastal Waters, East China Sea. Environ Monit Assess 129:315–320

    Article  PubMed  CAS  Google Scholar 

  4. Phillips DJH, Rainbow PS (1988) Barnacles and mussels as biomonitors of trace elements: a comparative study. Mar Ecol Prog Ser 49:83–93

    Article  CAS  Google Scholar 

  5. Alkarkhi AFM, Ismail N, Easa AM (2008) Assessment of arsenic and heavy metal contents in cockles (Anadara granosa) using multivariate statistical techniques. J Hazard Mater 150:783–789

    Article  Google Scholar 

  6. Mat I (1994) Arsenic and trace metals in commercially important bivalves, Anadara granosa and Paphia undulata. Bull Environ Contam Toxicol 52:833–839

    Article  PubMed  CAS  Google Scholar 

  7. Mat I, Maah MJ, Johari A (1994) Trace metals in sediments and potential availability to Anadara granosa. Arch Environ Contam Toxicol 27:54–59

    Article  CAS  Google Scholar 

  8. Tu NPC, Ha NN, Agusa T, Ikemoto T, Tuyen BC, Tanabe S, Takeuchi I (2010) Concentrations of trace elements in Meretrix spp. (Mollusca: Bivalva) along the coasts of Vietnam. Fish Sci 76:677–686

    Article  Google Scholar 

  9. Broom MJ (1985) The biology and culture of marine bivalve molluscs of the genus Anadara. International Center for Living Aquatic Resources Management, Manila

    Google Scholar 

  10. Tu NPC, Ha NN, Ikemoto T, Tuyen BC, Tanabe S, Takeuchi I (2008) Bioaccumulation and distribution of trace elements in tissues of giant river prawn Macrobrachium rosenbergii (Decapoda: Palaemonidae) from South Vietnam. Fish Sci 74:109–119

    Article  Google Scholar 

  11. Tu NPC, Ha NN, Ikemoto T, Tuyen BC, Tanabe S, Takeuchi I (2008) Regional variations in trace element concentrations in tissues of black tiger shrimp Penaeus monodon (Decapoda: Penaeidae) from South Vietnam. Mar Pollut Bull 57:858–866

    Article  PubMed  Google Scholar 

  12. US EPA (United States Environmental Protection Agency) (2000) Guidance for assessing chemical contaminant data for use in fish advisories, volume II. Risk assessment and fish consumption limits. US EPA, Washington, DC

  13. EC (European Commission) (2004) Report from Task 3.2.11: assessment of the dietary exposure to arsenic, cadmium, lead and mercury of the population of the EU Member States. EC, Brussels

  14. Han BC, Jeng WL, Chen RY, Fang GT, Hung TC, Tseng RJ (1998) Estimation of target hazard quotients and potential health risks for metals by consumption of seafood in Taiwan. Arch Environ Contam Toxicol 35:711–720

    Article  PubMed  CAS  Google Scholar 

  15. Han BC, Jeng WL, Hung TC, Ling YC, Shieh MJ, Chien LC (2000) Estimation of metal and organochlorine pesticide exposures and potential health threat by consumption of oysters in Taiwan. Environ Pollut 109:147–156

    Article  PubMed  CAS  Google Scholar 

  16. MacIntosh DL, Spengler JD, Ozkaynak H, Tsai L, Ryan PB (1996) Dietary exposures to selected metals and pesticides. Environ Health Perspect 104:202–209

    PubMed  CAS  Google Scholar 

  17. Eisler R (1981) Trace metal concentrations in marine organisms. Pergamon, New York

    Google Scholar 

  18. Boyden CR (1974) Trace element content and body size in molluscs. Nature 251:311–314

    Article  PubMed  CAS  Google Scholar 

  19. Phillips DJH (1976) The common mussel Mytilus edulis as an indicator of pollution by zinc, cadmium, lead and copper. I. Effects of environmental variables on uptake of metals. Mar Biol 38:59–69

    Article  CAS  Google Scholar 

  20. Joiris CR, Azokwu MI (1999) Heavy metals in the bivalve Anadara (Senilia) senilis from Nigeria. Mar Pollut Bull 38:618–622

    Article  CAS  Google Scholar 

  21. Riget F, Johansen P, Asmund G (1996) Influence of length on element concentrations in blue mussels (Mytilus edulis). Mar Pollut Bull 32:745–751

    Article  CAS  Google Scholar 

  22. Vinh LT (2006) Impact assessment of heavy metal discharges from the Hyundai-Vinashin shipyard on the southwest part of Van Phong Bay, Vietnam. In: Proceedings of the workshop on finalization of the projects VS/RDE/02: management tools of coastal environment for sustainable development, Nha Trang, Vietnam, 5–7 May 2006

  23. Hung NN, Ve NB, Buresh RJ, Bayley M, Watanabe T (2005) Sustainability of paddy soil fertility in Vietnam. In: Rice is life: scientific perspectives for the 21st century. Proceedings of the World Rice Research Conference, Tokyo and Tsukuba, Japan, 4–7 November 2005

  24. Denton GRW, Burdon-Jones C (1981) Influence of temperature and salinity on the uptake, distribution and depuration of mercury, cadmium and lead by the black-lip oyster Saccostrea echinata. Mar Biol 64:317–326

    CAS  Google Scholar 

  25. Jackim E, Morrison G, Steele R (1977) Effects of environmental factors on radiocadmium uptake by four species of marine bivalves. Mar Biol 40:303–308

    Article  CAS  Google Scholar 

  26. Rainbow PS (1985) The biology of heavy metals in the sea. Int J Environ Stud 25:195–211

    Article  CAS  Google Scholar 

  27. Debenay JP, Luan BT (2006) Foraminiferal assemblages and the confinement index as tools for assessment of saline intrusion and human impact in the Mekong Delta and neighbouring areas (Vietnam). Rev Micropaleontol 49:74–85

    Article  Google Scholar 

  28. Carpenter KE, Niem VH (eds) (1998) FAO species identification guide for fishery purposes. The living marine resources of the Western Central Pacific. Seaweeds, corals, bivalves and gastropods, vol 1. FAO, Rome, pp 1–686

  29. Sarkar SK, Cabral H, Chatterjee M, Cardoso I, Bhattacharya AK, Satpathy KK, Alam MA (2008) Biomonitoring of heavy metals using the bivalve molluscs in Sunderban mangrove wetland, northeast coast of Bay of Bengal (India): possible risks to human health. Clean Soil Air Water 36:187–194

    Article  CAS  Google Scholar 

  30. Griscom SB, Fisher NS, Luoma SN (2000) Geochemical influences on assimilation of sediment-bound metals in clams and mussels. Environ Sci Technol 34:91–99

    Article  CAS  Google Scholar 

  31. Abdullah MH, Sidi J, Aris AZ (2007) Heavy metals (Cd, Cu, Cr, Pb and Zn) in Meretrix meretrix Roding, water and sediments from estuaries in Sabah, North Borneo. Int J Environ Sci Educ 2:69–74

    Google Scholar 

  32. MARD (Vietnamese Ministry of Agriculture and Rural Development) (2010) Promulgating the lists of food safety criteria and maximum levels thereof in certain domestically-produced or imported foodstuffs of animal origin under the management of the Ministry of Agriculture and Rural Development (No. 29/2010/TT-BNNPTNT). MARD, Hanoi

  33. EC (European Commission) (2006) Setting maximum levels for certain contaminants in foodstuffs. Commission regulation (EC) No 1881/2006. Off J Eur Union 364:5–24

  34. National Shellfish Sanitation Program (2009) Guide for the control of molluscan shellfish 2007 revision. US Department of Health and Human Services, Food and Drug Administration, Center for Food Safety and Applied Nutrition. National Shellfish Sanitation Program, Washington DC

  35. NAFIQAD (National Agro-Forestry-Fisheries Quality Assurance Department) (2010) Report on results of harvesting status and post-harvest treatment June 2010. NAFIQAD, Hanoi (in Vietnamese)

  36. Satarug S, Moore MR (2004) Adverse health effects of chronic exposure to low-level cadmium in foodstuffs and cigarette smoke. Environ Health Perspect 112:1099–1103

    Article  PubMed  CAS  Google Scholar 

  37. Satarug S, Haswell-Elkins MR, Moore MR (2000) Safe levels of cadmium intake to prevent renal toxicity in human subjects. Br J Nutr 84:791–802

    PubMed  CAS  Google Scholar 

  38. Widmeyer J, Bendell-Young L (2008) Heavy metal levels in suspended sediments, Crassostrea gigas, and the risk to humans. Arch Environ Contam Toxicol 55:442–450

    Article  PubMed  CAS  Google Scholar 

  39. Cheng WWL, Gobas FAPC (2007) Assessment of human health risks of consumption of cadmium contaminated cultured oysters. Hum Ecol Risk Assess 13:370–382

    Article  CAS  Google Scholar 

  40. Liu C-W, Liang C-P, Huang FM, Hsueh Y-M (2006) Assessing the human health risks from exposure of inorganic arsenic through oyster (Crassostrea gigas) consumption in Taiwan. Sci Total Environ 361:57–66

    Article  PubMed  CAS  Google Scholar 

  41. Peshut PJ, Morrison RJ, Brooks BA (2008) Arsenic speciation in marine fish and shellfish from American Samoa. Chemosphere 71:484–492

    Article  PubMed  CAS  Google Scholar 

Download references

Acknowledgments

We express our sincere thanks to Dr. Todd Miller, Center for Marine Environmental Studies (CMES), Ehime University, for critical review of the manuscript. This study was partially supported by a grant from the Research Revolution 2002 (RR2002) of the Project for Sustainable Coexistence of Humans, Nature, and the Earth (FY2002) from the Ministry of Education, Culture, Sports, Science, and Technology (MEXT) of Japan, and Global COE Program from MEXT. The Grants-in-Aid for Scientific Research for Postdoctoral Fellows by the Japan Society for the Promotion of Science (No. 2109237 to NPCT, and No. 207871 to TA) are also acknowledged.

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Ichiro Takeuchi.

Rights and permissions

Reprints and permissions

About this article

Cite this article

Tu, N.P.C., Ha, N.N., Agusa, T. et al. Trace elements in Anadara spp. (Mollusca: Bivalva) collected along the coast of Vietnam, with emphasis on regional differences and human health risk assessment. Fish Sci 77, 1033–1043 (2011). https://doi.org/10.1007/s12562-011-0410-3

Download citation

  • Received:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s12562-011-0410-3

Keywords

Navigation