Abstract
Low-oxygen tolerance is important for aquaculture species, because exposure to hypoxia can result in heavy mortalities. This study evaluated the effects of strain, body weight, and gender on low-oxygen tolerance in channel catfish (Ictalurus punctatus) exposed to a lethal concentration of dissolved oxygen (0.1 mg/L). The variation in low-oxygen tolerance, assessed as the time to loss of equilibrium, of channel catfish from six strains (103KS, Kansas, KMix, Marion, Marion S, and Thompson) was examined. Catfish (15–179 g) showed a large variation in resistant time to hypoxia, ranging from 8 to 104 min, and both strain and body weight contributed significantly to this variation (P < 0.05). 103KS and Marion S strains had higher low-oxygen tolerance than the other strains, while the Marion strain had the poorest low-oxygen tolerance (P < 0.05). In addition to genetic background, body weight positively correlated with low-oxygen tolerance, but there were no significant differences between female and male catfish in low-oxygen tolerance. The results indicate that genetic background and body weight are important factors that contribute variations in low-oxygen tolerance.
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References
Aboagye DL, Allen PJ (2014) Metabolic and locomotor responses of juvenile paddlefish Polyodon spathula to hypoxia and temperature. Comp Biochem Phys A 169:51–59
Almeida-Val VM, Val AL, Duncan WP et al (2000) Scaling effects on hypoxia tolerance in the Amazon fish Astronotus ocellatus (Perciformes: Cichlidae): contribution of tissue enzyme levels. Comp Biochem Phys B 125:219–226
Bland JM, Altman DG (2004) The logrank test. BMJ 328:1073
Boyd CE, Tucker CS (2012) Pond aquaculture water quality management. Springer Science & Business Media, New York, US
Buentello JA, Gatlin DM, Neill WH (2000) Effects of water temperature and dissolved oxygen on daily feed consumption, feed utilization and growth of channel catfish (Ictalurus punctatus). Aquaculture 182:339–352
Burleson ML, Silva PE (2011) Cross tolerance to environmental stressors: effects of hypoxic acclimation on cardiovascular responses of channel catfish (Ictalurus punctatus) to a thermal challenge. J Therm Biol 36:250–254
Burleson ML, Wilhelm DR, Smatresk NJ (2001) The influence of fish size size on the avoidance of hypoxia and oxygen selection by largemouth bass. J Fish Biol 59:1336–1349
Burnham KP, Anderson DR (2004) Multimodel inference understanding AIC and BIC in model selection. Socio Meth Res 33:261–304
Cech JJ Jr, Massingill MJ, Vondracek B, Linden AL (1985) Respiratory metabolism of mosquitofish, Gambusia affinis: effects of temperature, dissolved oxygen, and sex difference. Environ Biol Fish 13:297–307
Dunham RA, Smitherman RO (1984) Ancestry and breeding of catfish in the United States, Cir. 273. Alabama Agricultural Experiment Station, Auburn, AL
Dunham RA, Ramboux AC, Perera DA (2014) Effect of strain on tolerance of low dissolved oxygen of channel X blue catfish hybrids. Aquaculture 420:25–28
Fox J, Andronic L, Ash M et al (2009) Rcmdr: R commander. R package version 1:5–4
Gjerde B, Odegard J, Thorland I (2011) Estimates of genetic variation in the susceptibility of Atlantic salmon (Salmo salar) to the salmon louse Lepeophtheirus salmonis. Aquaculture 314:66–72
Grambsch PM, Therneau TM (1994) Proportional hazards tests and diagnostics based on weighted residuals. Biometrika 81:515–526
Green BW, Rawles SD, Beck BH (2012) Response of channel × blue hybrid catfish to chronic diurnal hypoxia. Aquaculture 350:183–191
Henryon M, Jokumsen A, Berg P et al (2002) Genetic variation for growth rate, feed conversion efficiency, and disease resistance exists within a farmed population of rainbow trout. Aquaculture 209:59–76
Kaplan EL, Meier P (1958) Nonparametric estimation from incomplete observations. J Am Stat Assoc 53:457–481
Lin DY, Wei LJ (1989) The robust inference for the Cox proportional hazards model. J Am Stat Assoc 84:1074–1078
Miller RG Jr (2011) Survival analysis. John Wiley & Sons, New York
Nilsson GE, Östlund-Nilsson S (2008) Does size matter for hypoxia tolerance in fish? Biol Rev 83:173–189
Sloman K, Scott G, Wood S et al (2005) The effect of size on the physiological and behavioural responses of Oscar to hypoxia. Comp Biochem Phys A 141:176–177
Therneau T (2013) A package for survival analysis in S. R package version 2.37–4. URL http://CRAN.R-project.org/package=survival. Box. 980032, 23298–20032
Therneau TM, Grambsch PM (2000) Modeling survival data: extending the Cox model. Springer Science & Business Media, New York, US
Wang XZ, Liu SK, Jiang C et al (2017) Multiple across-strain and within-strain QTLs suggest highly complex genetic architecture for hypoxia tolerance in channel catfish. Mol Gen Genomics 292:63–76
Welker TL, Mcnulty ST, Klesius PH (2007) Effect of sublethal hypoxia on the immune response and susceptibility of channel catfish, Ictalurus punctatus, to enteric septicemia. J World Aquacult Soc 38:12–23
Acknowledgements
This work was supported by a grant from the USDA National Institute of Food and Agriculture (grant number 2014-70007-22395). The authors thank Dr. Ash Abebe for precious advice with statistical analysis. Thanks are given to C. Jiang, T. Zhou, N. Li, and H. Li for their help with fish culture and hypoxia challenge.
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All procedures involving the handling and treatment of fish in this study were approved by the Institutional Animal Care and Use Committee (IACUC) at Auburn University.
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Wang, X., Liu, S., Dunham, R. et al. Effects of strain and body weight on low-oxygen tolerance of channel catfish (Ictalurus punctatus). Aquacult Int 25, 1645–1652 (2017). https://doi.org/10.1007/s10499-017-0125-2
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DOI: https://doi.org/10.1007/s10499-017-0125-2