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Fisheries Science

, Volume 85, Issue 6, pp 1067–1075 | Cite as

Effects of total dissolved gas supersaturated water at varying suspended sediment concentrations on the survival of rock carp Procypris rabaudi

  • Cuixia Feng
  • Na Li
  • Yuanming Wang
  • Xiaoqing LiuEmail author
  • Xiaotao Shi
  • Chenghua Fu
  • Zhu Jiang
  • Yao Yang
  • Haoran Shi
Original Article Environment

Abstract

High total dissolved gas (TDG) levels and excessive suspended sediment (SS) concentrations greatly threaten the survival of fish downstream of dams when flood discharge occurs. However, few studies have investigated the impacts of TDG and SS on fish. To evaluate the effects of TDG and SS on rock carp, juveniles were exposed to 125, 130, 135 and 140% TDG supersaturated water with SS concentrations of 0, 200, 600 and 1000 mg/l, respectively, and after the exposure period, the rock carp showed noticeable abnormal behaviours and signs of gas bubble disease. The survival rate decreased with increases in the TDG levels and SS concentrations. Moreover, an increase in the SS concentration in the TDG supersaturated water resulted in a decrease in the median survival time (ST50). Combined exposure to TDG and SS exerted a significant effect on the survival of rock carp. This study indicates that TDG supersaturated water with SS might be a notable threat to rock carp survival during flood discharge.

Keywords

Total dissolved gas supersaturation (TDG) Suspended sediment (SS) Rock carp Procypris rabaudi Median survival time (ST50

Notes

Acknowledgements

This work was supported by the National Natural Science Foundation of China (Grant No. 51509213), Open Fund Research at the State Key Laboratory of Hydraulics and Mountain River Engineering, Sichuan University, China (Grant No. Skhl1823), Academic Cultivation Project of Key Laboratory of Fluid and Power Machinery of the Education Ministry, Xihua University (Grant Nos. SBZDPY-11-09 and SBZDPY-11-10), Young Scholars Program of Xihua University (Grant No. 0220170212), Innovation Fund of Postgraduate, Xihua University (Grant No. ycjj2018190) and Open Fund of Engineering Research Center of Eco-environment in Three Gorges Reservoir Region, Ministry of Education, China Three Gorges University (Grant No. KF2017-03).

References

  1. Bai YBLJ, Chen XR (2012) Research progress of impacts of sediment flushing on downstream fish. J Sediment Res 1:74–80 (in Chinese with English abstract) Google Scholar
  2. Beeman JW, Venditti DA, Morris RG, Gadomski DM, Adams BJ, Vanderkooi SP, Robinson TC, Maule AG (2003) Gas bubble disease in resident fish below Grand Coulee Dam: final report of research. USBR, BoiseGoogle Scholar
  3. Beiningen KT, Ebel WJ (1970) Effect of John Day Dam on dissolved nitrogen concentrations and salmon in the Columbia River. T Am Fish Soc 99:664–671CrossRefGoogle Scholar
  4. Bouck GR (1980) Etiology of gas bubble disease. T Am Fish Soc 109:703–707CrossRefGoogle Scholar
  5. Cao L, Liang RF, Tuo YC, Li Y, Li KF (2016a) Influence of total dissolved gas-supersaturated water on silver carp (Hypophthalmichthys molitrix). WSE 9:324–328Google Scholar
  6. Cao L, Li K, Liang R, Chen S, Jiang W, Li R (2016b) The tolerance threshold of Chinese sucker to total dissolved gas supersaturation. Aquac Res 47:2804–2813CrossRefGoogle Scholar
  7. Changjiang Water Resources Commission of the Ministry of Water Resources (2016) Changjiang Sediment Bulletin. Changjiang press, Beijing (in Chinese)Google Scholar
  8. Chen SC, Liu XQ, Jiang W, Li KF, Du J, Shen DZ, Gong Q (2012) Effects of total dissolved gas supersaturated water on lethality and catalase activity of Chinese sucker (Myxocyprinus asiaticus Bleeker). J Zhejiang Univ Sci B 13:791–796PubMedPubMedCentralCrossRefGoogle Scholar
  9. Counihan TD, Miller AI, Mesa MG, Parsely MJ (1998) The effects of dissolved gas supersaturation on white sturgeon larvae. T Am Fish Soc 127:316–322CrossRefGoogle Scholar
  10. Ding TP, Gao JF, Tian SH, Wang SH, Li M, Wang CY, Luo XR (2016) Chemical and isotopic characters of the water and suspended particulate materials in the Yellow River and their geological and environmental implications. Acta Geol Sin-Engl 90:285–351CrossRefGoogle Scholar
  11. Ebel WJ, Raymond HL (1976) Effect of atmospheric gas supersaturation on salmon and steelhead trout of the Snake and Columbia rivers. Marin Fish Rev 387:1–14Google Scholar
  12. Erich S (2000) Effects of sediment flushing on fish and invertebrates in Swiss alpine rivers. International Workshop and Symposium on Reservoir Sedimentation Management, ToyamaGoogle Scholar
  13. Feng JJ, Li R, Liang RF, Shen X (2014) Eco-environmentally friendly operational regulation: an effective strategy to diminish the TDG supersaturation of reservoirs. Hydrol Earth Syst Sc 18:1213–1223CrossRefGoogle Scholar
  14. Garric J, Migeon B, Vindimian E (1990) Lethal effects of draining on brown trout. A predictive model based on field and laboratory studies. Water Res 24:59–65CrossRefGoogle Scholar
  15. Gültepe N, Ates O, Hisar O, Beydemir S (2011) Carbonic anhydrase activities from the rainbow trout lens correspond to the development of acute gas bubble disease. J Aquat Anim Health 23:134–139PubMedCrossRefPubMedCentralGoogle Scholar
  16. Hasan MR, Macintosh DJ (1986) Acute toxicity of ammonia to common carp fry. Aquaculture 54:97–107CrossRefGoogle Scholar
  17. Henley WF, Patterson MA, Neves RJ, Lemly AD (2000) Effects of sedimentation and turbidity on lotic food webs: a concise review of natural resource managers. Rev Fish Sci 8:125–139CrossRefGoogle Scholar
  18. Huang X (2010) Effects of TDG supersaturation due to high dam flood discharge on survival in juvenile rock carp. PhD dissertation, Sichuan University of Urban Hydraulic Engineering and Water Security, Chengdu (in Chinese) Google Scholar
  19. Jensen JOT, Schnute J, Alderdice DF (1986) Assessing juvenile salmonid responses to gas supersaturation using a general multivariate dose–response model. Can J Fish Aquat Sci 43:1694–1709CrossRefGoogle Scholar
  20. Kleinbaum DG, Klein M (2005) Survival analysis. Statistics for biology and health. Springer, New YorkGoogle Scholar
  21. Krise WF (1993) Effects of one-year exposures to gas supersaturation on lake trout. Prog Fish Cult 55:169–176CrossRefGoogle Scholar
  22. Lake RG, Hinch SG (1999) Acute effects of suspended sediment angularity on juvenile coho salmon (Oncorhynchus kisutch). Can J Fish Aquat Sci 56:862–867CrossRefGoogle Scholar
  23. Lee ET (1992) Statistical methods for survival data analysis. John Wiley & Sons, New YorkGoogle Scholar
  24. Li R, Li J, Li K, Qu LJ, Feng J (2009) Field observation of total dissolved gas supersaturation downstream of Ertan high dam. IAHS Publ 335:254–258Google Scholar
  25. Liu J (2004) A quantitative analysis on threat and priority of conservation order of the endemic fishes in upper reaches of the Yangtze River. China Environ Sci 24:395–399 (in Chinese with English abstract) Google Scholar
  26. Marcello RA, Fairbanks RB (1976) Gas bubble disease of Atlantic menhaden, Brevoortia tyrannus, at a coastal nuclear power plant. In: Fickeisen DH, Schneider MJ (eds) Gas bubble disease. Technical Information Center, Energy Research and Development Administration, Oak Ridge, pp 75–80Google Scholar
  27. Marsh MC, Gorham FP (1905) The gas disease in fishes. Rep US Bur Fish 343–376Google Scholar
  28. Meekin TK, Turner BK (1974) Tolerance of salmonid eggs, juveniles and squawfish to supersaturated nitrogen. Nitrogen supersaturation investigations in the mid-Columbia River. Washington Department of Fisheries, Olympia, pp 78–126Google Scholar
  29. Mesa MG, Weiland LK, Maule AG (2000) Progression and severity of gas bubble trauma in juvenile salmonids. T Am Fish Soc 129:174–185CrossRefGoogle Scholar
  30. Newcombe CP, Macdonald DD (1991) Effects of suspended sediments on aquatic ecosystems. N Am J Fish Manag 11:72–82CrossRefGoogle Scholar
  31. Pauley GB, Nakatani RE (1967) Histopathology of “gas-bubble” disease in salmon fingerlings. J Fish Res Board Can 24:867–871CrossRefGoogle Scholar
  32. Pratap CD, Ayyappan S, Jena JK, Das BK (2004) Acute toxicity of ammonia and its sub-lethal effects on selected haematological and enzymatic parameters of mrigal, Cirrhinus mrigala (Hamilton). Aquac Res 35:134–143CrossRefGoogle Scholar
  33. Qiu XC, Tanoue W, Kawaguchi A, Yanagawa T, Seki M, Shimasaki Y, Honjo T, Oshima Y (2017) Interaction patterns and toxicities of binary and ternary pesticide mixtures to Daphnia magna estimated by an accelerated failure time model. Sci Total Environ 607–608:367–374PubMedCrossRefPubMedCentralGoogle Scholar
  34. Qiu XC, Iwasaki N, Chen K, Shimasaki Y, Oshima Y (2019a) Tributyltin and perfluorooctane sulfonate play a synergistic role in promoting excess fat accumulation in Japanese medaka (Oryzias latipes) via in ovo exposure. Chemosphere 220:687–695PubMedCrossRefPubMedCentralGoogle Scholar
  35. Qiu XC, Kim S, Kang IJ, Hano T, Shimasaki Y, Oshima Y (2019b) Combined toxicities of tributyltin and polychlorinated biphenyls on the development and hatching of Japanese medaka (Oryzias latipes) embryos via in ovo nanoinjection. Chemosphere 225:927–934CrossRefGoogle Scholar
  36. Qu L, Li R, Li J, Li KF, Deng Y (2011) Field observation of total dissolved gas supersaturation of high-dams. Sci China Ser E 54:156–162CrossRefGoogle Scholar
  37. Renfro WC (1963) Gas-bubble mortality of fishes in Galveston Bay, Texas. T Am Fish Soc 92:320–322CrossRefGoogle Scholar
  38. Richardson J, Rowe DK, Smith JP (2001) Effects of turbidity on the migration of juvenile banded kokopu (Galaxias fasciatus) in a natural stream. N Z J Mar Fresh 35:191–196CrossRefGoogle Scholar
  39. Rowe D, Hicks M, Smith J, Williams E (2009) Lethal concentrations of suspended solids for common native fish species that are rare in new Zealand rivers with high suspended solids loads. N Z J Mar Fresh 43:1029–1038CrossRefGoogle Scholar
  40. Rucker RR, Kangas PM (1974) Effect of nitrogen supersaturated water on coho and Chinook salmon. Prog Fish Cult 36:152–156CrossRefGoogle Scholar
  41. Servizi JA, Martens DW (1991) Effect of temperature, season, and fish size on acute lethality of suspended sediments to coho salmon (Oncorhynchus kisutch). Can J Fish Aquat Sci 48:493–497CrossRefGoogle Scholar
  42. Stroud RK, Bouck GR, Nebeker AV (1975) Pathology of acute and chronic exposure of salmonid fishes to supersaturated water. In: Adams WA (ed) Chemistry and physics of aqueous gas solutions. The Electrochemical Society, Princeton, pp 435–449Google Scholar
  43. Wang YM, Li KF, Li J, Li R, Deng Y (2015a) Tolerance and avoidance characteristics of Prenant’s schizothoracin Schizothorax prenanti to total dissolved gas supersaturated water. N Am J Fish Manag 35:827–834CrossRefGoogle Scholar
  44. Wang YM, Zhang LL, Zeng C, Li KF (2015b) Tolerance and avoidance responses of Schizothorax pernanti to total dissolved gas supersaturation. J Hydraul Eng 46:480–488Google Scholar
  45. Wang YM, An RD, Li Y, Li KF (2017) Swimming performance of rock carp Procypris rabaudi and Prenant’s schizothoracin Schizothorax prenanti acclimated to total dissolved gas supersaturated water. N Am J Fish Manag 37:827–834CrossRefGoogle Scholar
  46. Water Resources Protection Bureau of Yangtze River (1983) Investigation of gas bubble disease and spill of Gezhouba Dam. Water Resources Protection Bureau of Yangtze River, Wuhan (in Chinese) Google Scholar
  47. Weitkamp DE, Katz M (1980) A review of dissolved gas supersaturation literature. T Am Fish Soc 109:659–702CrossRefGoogle Scholar
  48. Wenger AS, Johansen JL, Jones GP (2012) Increasing suspended sediment reduces foraging, growth and condition of a planktivorous damselfish. J Exp Mar Biol Ecol 428:43–48CrossRefGoogle Scholar
  49. Westgard RL (1964) Physical and biological aspects of gas-bubble disease in impounded adult Chinook salmon at McNary spawning channel. T Am Fish Soc 93:306–309CrossRefGoogle Scholar
  50. Woodbury LA (1942) A sudden mortality of fishes accompanying a supersaturation of oxygen in Lake Waubesa, Wisconsin. T Am Fish Soc 71:112–117CrossRefGoogle Scholar
  51. Wyatt EJ, Beiningen KT (1971) Nitrogen gas bubble disease related to a hatchery water supply from the fore bay of a high head re-regulating dam. Fish Commission of Oregon, PortlandGoogle Scholar
  52. Yang GW, An LG (1999) A review on the researches of fish mucus cells. J Fish China 4:403–408 (in Chinese) Google Scholar
  53. Yuan Y, Yuan Q, Wang YM, An R, Li KF (2017a) Acute and chronic lethality of total dissolved gas supersaturated water on Leptobotia elongata. Adv Eng Sci 49:56–61 (in Chinese with English abstract) Google Scholar
  54. Yuan Q, Yuan Y, Wang YM, Li Y, Li KF (2017b) Avoidance characteristics of Leptobotia elongata to total dissolved gas supersaturation. J Hydroecol 38:77–81 (in Chinese with English abstract) Google Scholar
  55. Yuan Y, Wang YM, Zhou C, An RD, Li KF (2018) Tolerance of Prenant’s schizothoracin Schizothorax prenanti to total dissolved gas supersaturated water at varying temperatures. N Am J Aquacult 80:107–115CrossRefGoogle Scholar
  56. Zhang YR, Du QC, Wang YM, Li KF (2014) Effects of TDG supersaturated water with sediment on juvenile Schizothorax prenanti. J Hydraul Eng 45:1029–1037 (in Chinese with English abstract) Google Scholar

Copyright information

© Japanese Society of Fisheries Science 2019

Authors and Affiliations

  1. 1.Key Laboratory of Fluid and Power Machinery, Ministry of EducationXihua UniversityChengduChina
  2. 2.School of Energy and Power EngineeringXihua UniversityChengduChina
  3. 3.State Key Laboratory of Hydraulics and Mountain River EngineeringSichuan UniversityChengduChina
  4. 4.Engineering Research Center of Eco-environment in Three Gorges Reservoir Region, Ministry of EducationThree Gorges UniversityYichangChina

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