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Preliminary Study of the Effects of CO2 on the Survival and Gowth of Olive Flounder (Paralichthys olivaceus) Juveniles

  • Hwang, In-Joon (Department of Marine Biology, Pukyong National University) ;
  • Park, Mun-Chang (Department of Marine Biology, Pukyong National University) ;
  • Baek, Hea-Ja (Department of Marine Biology, Pukyong National University)
  • Published : 2009.12.31

Abstract

As a result of human industrial development, carbon dioxide ($CO_2$) is currently accumulating in the atmosphere and dissolving into the oceans. Sequestration into the deep sea has been proposed as a possible solution to this increasing atmospheric $CO_2$, although the impact of such a program on marine ecosystems is unknown. We examined the effects of increased $CO_2$ levels on the growth of the olive flounder, Paralichthys olivaceus. Juvenile olive flounder 40 days post hatching were exposed to two levels of $CO_2$ (3.60-7.55 and 4.05-11.46 kPa) in running seawater for 26 days. During the exposure period, the pH and $CO_2$ levels of the water were measured, and the numbers of dead individuals were counted in each aquarium. Following the exposure period, the total lengths (mm) and body weights (mg) of the juvenile fish were measured. Both $CO_2$ treatments significantly increased fish mortality compared to controls ($19.87\pm4.53%$ vs. 7.14% and $75.96\pm1.36%$ vs. 7.14% for high and low doses, respectively). After the high $CO_2$ treatment, total length ($14.98\pm6.58$ mm vs. $19.52\pm1.83$ mm) and body weight ($28.92\pm13.85$ mg vs. $67.35\pm18.32$ mg) of the exposed flounder were reduced compared to the control fish; however, no significant differences in these values were observed after the low $CO_2$ dose. These results suggested that $CO_2$ exposure inhibits growth in the juvenile stage and that $CO_2$-enriched seawater is toxic in the early life stages of olive flounder.

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References

  1. Adams EE, Caulfield JA, Herzog HJ and Auerbach DI. 1997. Impacts of reduced pH from ocean CO$_2$ disposal: sensitivity of zooplankton mortality to model parameters. Waste Management 17, 375-380 https://doi.org/10.1016/S0956-053X(97)10038-1
  2. Auerbach DI, Caulfield JA, Adams EE and Herzog HJ. 1997. Impacts of ocean CO$_2$ disposal on marine life: A toxicological assessment intergrating constant-concentration laboratory assay data with variable-concentration field exposure. Environ Model Assess 2, 333-343 https://doi.org/10.1023/A:1019029931755
  3. Brouwer M, Larkin P, Brown-Peterson N, King C, Manning S and Denslow N. 2004. Effects of hypoxia on gene and protein expression in the blue crab, Callinectes sapidus. Mar Environ Res 58, 787-792 https://doi.org/10.1016/j.marenvres.2004.03.094
  4. Cole KH, Stegen GR and Spencer D. 1995. The capacity of the deep oceans to absorb carbon dioxide. In: Direct ocean disposal of carbon dioxide. Handa N and Ohsumi T, eds. Terra Sceintific Publishing Company Tokyo, Japan., 143-152
  5. Feely RA, Sabine CL, Lee K, Berelson W, Kleypas J, Fabry VJ and Millero FJ. 2004. Impact of anthro-pogenic CO$_2$ on the CaCO$_3$ system in the oceans. Science 305, 362-366 https://doi.org/10.1126/science.1097329
  6. Fivelstad S, Olsen AB, Kluften H, Ski H and Stefansson S. 1999. Effects of carbon dioxide on Atlantic salmon (Salmo salar L.) smolts, at constant pH in bicarbonate rich freshwater. Aquaculture 178, 171-187 https://doi.org/10.1016/S0044-8486(99)00125-8
  7. Fivelstad S, Olsen AB, Asgard T, Baeverfjord G, Rasmussen T, Vindheim T and Stefansson S. 2003. Long-term sublethal effects of carbon dioxide on Atlantic salmon smolts (Salmo salar L.): ion regula-tion, haematology, element composition, nephrocal-cinosis and growth parameters. Aquaculture 215, 301-319 https://doi.org/10.1016/S0044-8486(02)00048-0
  8. Fivelstad S, Waagb$\o$ R, Stefansson S, Olsen AB. 2007. Impacts of elevated water carbon dioxide partial pre-ssure at two temperatures on Atlantic salmon (Salmo salar L.) parr growth and haematology. Aquaculture. 269. 241-249 https://doi.org/10.1016/j.aquaculture.2007.05.039
  9. Gazeau F, Quiblier C, Jansen JM, Gattuso JP, Middelburg JJ and Heip CHR. 2007. Impact of elevated CO2 on shellfish calcification. Geophys Res Lett 34, 5
  10. Grottum JA and Sigholt T. 1996. Acute toxicity of carbon dioxide on European seabass (Dicentrachus labrax): Mortality and effects on plasma ions. Comp Biochem Physiol 115, 323-327 https://doi.org/10.1016/S0300-9629(96)00100-4
  11. Hayashi M, Kita J and Ishimatsu A. 2004. Acid-base responses to lethal aquatic hypercapnia in three marine fish. Mar Biol 144, 153-160 https://doi.org/10.1007/s00227-003-1172-y
  12. Iglesias-Rodriguez MD, Halloran PR, Rickaby REM, Hall IR, Colmenero-Hidalgo E, Gittins JR, Green DRH, Tyrrell T, Gibbs SJ, von Dassow P, Rehm E, Virginia Armbrust E and Boessenkooland KP. 2008. Phyto-plankton calcification in a high-COCO$_2$ world. Science 320, 336-340 https://doi.org/10.1126/science.1154122
  13. IPCC. 2001. Climate change 2001: Synthesis Report. A Contribution of Working Groups I, II and III to the Third Assessment Report of the Intergovernmental Panel on Climate Change. University Press, Cam-bridge
  14. Ingermann RL, Holcomb M, Robinson ML and Cloud JG. 2002. Carbon dioxide and pH affect sperm motility of white sturgeon (Acipenser transmontanus). J Exp Biol 205, 2885-2890
  15. Ishimatsu A, Kikkawa T, Hayashi M, Lee KS and Kita J. 2004. Effects of CO$_2$ on marine fish: Larvae and adults. J Oceanogr 60, 731-741 https://doi.org/10.1007/s10872-004-5765-y
  16. Ishimatsu A, Hayashi M and Kikkawa T. 2008. Fishes in high-CO$_2$, acidified oceans. Mar Ecol Prog Ser 373, 295-302 https://doi.org/10.3354/meps07823
  17. Kikkawa T, Ishimatsu A and Kita J. 2003. Acute CO$_2$ tolerance during the early developmental stages of four marine teleost. Environ Toxicol 18, 375-382 https://doi.org/10.1002/tox.10139
  18. Kaufman RC, Houck AG. Cech Jr. JJ. 2007. Effects of temperature and carbon dioxide on green sturgeon blood-oxygen equilibria. Environ Biol Fish 79, 201-210 https://doi.org/10.1007/s10641-006-9176-3
  19. Lee KS, Kita J and Ishimatsu A. 2003. Effects of lethal levels of environmental hypercapnia on cardio-vascular and blood-gas status in yellowtail, Seriola quinqueradiata. Zool Sci 20, 417-422 https://doi.org/10.2108/zsj.20.417
  20. Michaelidis B, Spring A and P$\ddot{o}$rtner HO. 2007. Effects of long-term acclimation to environmental hypercapnia on extracellular acid-base status and metabolic capacity in Mediterranean fish Sparus aurata. Mar Biol 150, 1417-1429 https://doi.org/10.1007/s00227-006-0436-8
  21. Ormerod B and Angel M. 1996. Ocean storage of carbon dioxide. Workshop 2-Environmental Impact. IEA Greenhouse and Gas R&D Programme, Cheltenham, UK. 131
  22. Parsons TR, Maita Y and Lalli CM. 1984. A Manual of Chemical and Biological Methods for Seawater Analysis. Pergamon, Oxford, U.K., 141-149
  23. Randall DJ. 1970. Gas exchange in fish. In: Hoar WS and Randall DJ,_eds. Fish Physiology IV. Academic Press, New York, U.S.A., 253-286
  24. Sabine CL, Feely RA, Gruber N, Key RM, Lee K, Bullister JL, Wanninkhof R, Wong CS, Wallace DWR, Tilbrook B, Millero FJ, Peng TH, Kozyr A, Ono T and Rios AF. 2004. The oceanic sink for anthropogenic CO$_2$. Science 305, 367-371 https://doi.org/10.1126/science.1097403
  25. Sato T and Sato K. 2002. Numerical prediction of the dilution process and its biological impacts in CO$_2$ ocean sequestration. Mar Sci Technol 6, 169-180 https://doi.org/10.1007/s007730200005