Skip to main content

The Effect of Hypoxia on Fish Swimming Performance and Behaviour

  • Chapter
  • First Online:

Abstract

Oxygen depletion, hypoxia, can be a common stressor in aquatic habitats, including aquaculture. Hypoxia limits aerobic swimming performance in fish, by limiting their aerobic metabolic scope. Hypoxia also elicits changes in spontaneous swimming activity, typically causing a decrease in swimming speed in sedentary species and an increase in active species. However, fish do have the capacity to avoid hypoxia and actively choose well-oxygenated areas. Hypoxia causes differences in fish behaviour in schools, it may reduce school density and size and influence activities such as shuffling within schools. Hypoxia also influences predator–prey interactions, in particular by reducing fast-start performance. Thus, through effects on swimming, hypoxia can have profound effects on species distributions in the field. In aquaculture, effects of hypoxia may be particularly significant in sea cages. It is therefore important to understand the nature and thresholds of effects of hypoxia on swimming activity to extrapolate to potential impacts on fish in aquaculture.

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

Buying options

Chapter
USD   29.95
Price excludes VAT (USA)
  • Available as PDF
  • Read on any device
  • Instant download
  • Own it forever
eBook
USD   129.00
Price excludes VAT (USA)
  • Available as EPUB and PDF
  • Read on any device
  • Instant download
  • Own it forever
Softcover Book
USD   169.99
Price excludes VAT (USA)
  • Compact, lightweight edition
  • Dispatched in 3 to 5 business days
  • Free shipping worldwide - see info
Hardcover Book
USD   169.99
Price excludes VAT (USA)
  • Durable hardcover edition
  • Dispatched in 3 to 5 business days
  • Free shipping worldwide - see info

Tax calculation will be finalised at checkout

Purchases are for personal use only

Learn about institutional subscriptions

References

  • Abrahams MV, Colgan P (1985) Risk of predation, hydrodynamic efficiency and their influence on school structure. Environ Biol Fishes 13:195–202

    Google Scholar 

  • Beamish FWH (1978) Swimming capacity. In: Hoar WS, Randall DJ (eds) Fish physiology, vol VII. Academic Press, New York, pp 101–187

    Google Scholar 

  • Bejda AJ, Studholme AL, Olla BL (1987) Behavioural responses of red hake, Urophycis chuss, to decreasing concentrations of dissolved oxygen. Environ Biol Fishes 19:611–621

    Google Scholar 

  • Boisclair D, Tang M (1993) Empirical analysis of the influence of swimming pattern on the net energetic cost of swimming in fishes. J Fish Biol 42:169–183

    Google Scholar 

  • Brady DC, Targett TE, Tuzzolino DM (2009) Behavioral responses of juvenile weakfish (Cynoscion regalis) to diel-cycling hypoxia: swimming speed, angular correlation, expected displacement, and effects of hypoxia acclimation. Can J Fish Aquat Sci 66:415–424

    Google Scholar 

  • Breitburg DL, Steinberg N, DuBeau S, Cooksey C, Houde ED (1994) Effects of low dissolved oxygen on predation on estuarine fish larvae. Mar Ecol Prog Ser 104:235–246

    Google Scholar 

  • Breitburg DL, Rose KA, Cowan JH (1999) Linking water quality to larval survival: predation mortality of fish larvae in an oxygen-stratified water column. Mar Ecol Prog Ser 178:39–54

    Google Scholar 

  • Brierly AS, Cox MJ (2010) Shapes of krill swarms and fish schools emerge as aggregation members avoid predators and access oxygen. Cur Biol 20(19):1758–1762

    Google Scholar 

  • Brown EJ, Bruce M, Pether S, Herbert NA (2011) Do swimming fish always grow fast? Investigating the magnitude and physiological basis of exercise-induced growth in juvenile New Zealand yellowtail kingfish, Seriola lalandi. Fish Physiol Biochem 37:327–336

    PubMed  CAS  Google Scholar 

  • Bumann D, Krause J, Rubenstein D (1997) Mortality risk of spatial position in animal groups: the danger of being in the front. Behaviour 134:1063–1076

    Google Scholar 

  • Burgetz IJ, Rojas-Vargas A, Hinch SG, Randall DJ (1998) Initial recruitment of anaerobic metabolism during sub-maximal swimming in rainbow trout (Oncorhynchus mykiss). J Exp Biol 201:2711–2721

    PubMed  Google Scholar 

  • Burleson ML, Smatresk NJ, Milsom WK (1992) Afferent inputs associated with cardioventilatory control in fish. In: Hoar WS, Randall DJ, Farrell AP (eds) Fish Physiology, vol XIIB. Academic Press, New York, pp 389–426

    Google Scholar 

  • Bushnell PG, Steffensen JF, Johansen K (1984) Oxygen consumption and swimming performance in hypoxia-acclimated rainbow trout Salmo gairdneri. J Exp Biol 113:225–235

    Google Scholar 

  • Cannas M, Domenici P, Lefrançois C (2012) The effect of hypoxia on ventilation frequency in startled common sole Solea solea. J Fish Biol 80:2636–2642

    PubMed  CAS  Google Scholar 

  • Chabot D, Claireaux G (2008) Environmental hypoxia as a metabolic constraint on fish: the case of Atlantic cod, Gadus morhua. Mar Pollut Bull 57:287–294

    PubMed  CAS  Google Scholar 

  • Chabot D, Dutil JD (1999) Reduced growth of Atlantic cod in non-lethal hypoxic conditions. J Fish Biol 55:472–491

    Google Scholar 

  • Chapman LJ, McKenzie DJ (2009) Behavioral responses and ecological consequences. In: Richards JG, Farrell AP, Brauner CJ (eds) Hypoxia. Elsevier, London, pp 25–77

    Google Scholar 

  • Claireaux G, Chabot D (2005) A review of the impact of environmental hypoxia on fish: the case of Atlantic cod. Comp Biochem Physiol 141A:S177

    Google Scholar 

  • Claireaux G, Webber DM, Lagardere JP, Kerr SR (2000) Influence of water temperature and oxygenation on the aerobic metabolic scope of Atlantic cod (Gadus morhua). J Sea Res 44:257–265

    Google Scholar 

  • Claireaux G, Handelsman C, Standen E, Nelson JA (2007) Thermal and temporal stability of swimming performance in the European sea bass. Physiol Biochem Zool 80(2):186–196

    PubMed  Google Scholar 

  • Cook DG, Herbert NA (2012) The physiological and behavioural response of juvenile kingfish (Seriola lalandi) differs between escapable and inescapble progressive hypoxia. J Exp Mar Biol Ecol 413:138–144

    Google Scholar 

  • Cook DG, Wells RMG, Herbert NA (2011) Anaemia adjusts the aerobic physiology of snapper (Pagrus auratus) and modulates hypoxia avoidance behaviour during oxygen choice presentations. J Exp Biol 214:2927–2934

    PubMed  Google Scholar 

  • Dahlberg ML, Shumway DL, Doudoroff O (1968) Influence of dissolved oxygen and carbon dioxide on swimming performance of largemouth bass and coho salmon. J Fish Res Bd Can 25:49–70

    CAS  Google Scholar 

  • Dean TL, Richardson J (1999) Responses of seven species of native freshwater fish and a shrimp to low levels of dissolved oxygen. N Z J Mar Freshw Res 33(1):99–106

    Google Scholar 

  • Diaz RJ (2001) Overview of hypoxia around the world. J Environ Qual 30:275–281

    PubMed  CAS  Google Scholar 

  • Diaz RJ, Rosenberg R (2008) Spreading dead zones and consequences for marine ecosystems. Science 321:926–929

    PubMed  CAS  Google Scholar 

  • Dizon AE (1977) Effect of dissolved oxygen concentration and salinity on swimming speed of two species of tunas. Fish B-NOAA 75:649–653

    Google Scholar 

  • Domenici P, Blake RW (1997) The kinematics and performance of fish fast start swimming. J Exp Biol 200:1165–1178

    PubMed  Google Scholar 

  • Domenici P, Steffensen JF, Batty RS (2000a) The effect of progressive hypoxia on swimming activity and schooling in Atlantic herring. J Fish Biol 57:1526–1538

    Google Scholar 

  • Domenici P, Batty RS, Simila T (2000b) Spacing of wild schooling herring while encircled by killer whales. J Fish Biol 57:831–836

    Google Scholar 

  • Domenici P, Ferrari RS, Steffensen JF, Batty RS (2002) The effect of progressive hypoxia on school structure and dynamics in Atlantic herring Clupea harengus. Proc R Soc B 269:2103–2111

    PubMed  Google Scholar 

  • Domenici P, Claireaux G, McKenzie DJ (2007a) Environmental constraints upon locomotion and predator–prey interactions in aquatic organisms: an introduction. Phil Trans R Soc 362:1929–1936

    CAS  Google Scholar 

  • Domenici P, Lefrançois C, Shingles A (2007b) The effect of hypoxia on the antipredator behaviours of fishes. Philos Trans R Soc 362:2105–2121

    CAS  Google Scholar 

  • Dommasnes A, Rey F, Røttingen I (1994) Reduced oxygen concentrations in herring wintering areas. ICES J Mar Sci 51:63–69

    Google Scholar 

  • Dupont-Prinet A, Chatain B, Grima L, Vandeputte M, Claireaux G, McKenzie DJ (2010) Physiological mechanisms underlying a trade-off between growth rate and tolerance of feed deprivation in the European sea bass (Dicentrarchus labrax). J Exp Biol 213:1143–1152

    PubMed  CAS  Google Scholar 

  • Eaton RC, Hackett JT (1984) The role of Mauthner cells in fast-starts involving escape in teleost fish. In: Eaton RC (ed) Neural mechanisms of startle behavior. Plenum Press, New York, pp 213–266

    Google Scholar 

  • Ellis T, Howell BR, Hughes RN (1997) The cryptic responses of hatchery-reared sole to a natural sand substratum. J Fish Biol 51:389–401

    Google Scholar 

  • Farmer CG, Jackson DC (1998) Air-breathing during activity in the fishes Amia calva and Lepisosteus oculatus. J Exp Biol 201(7):943–948

    PubMed  Google Scholar 

  • Farrell AP, Gamperl AK, Birtwell IK (1998) Prolonged swimming, recovery and repeat swimming performance of mature sockeye salmon Oncorhynchus nerka exposed to moderate hypoxia and pentachlorophenol. J Exp Biol 201:2183–2193

    PubMed  CAS  Google Scholar 

  • Fisher P, Rademacher K, Kils U (1992) In situ investigations on the respiration and behaviour of the eelpout Zoarces viviparus under short-terms hypoxia. Mar Ecol Prog Ser 88:181–184

    Google Scholar 

  • Fitzgibbon QP, Seymour RS, Buchanan J, Musgrove R, Carragher J (2010) Effects of hypoxia on oxygen consumption, swimming velocity and gut evacuation in southern bluefin tuna (Thunnus maccoyii). Environ Biol Fish 89:59–69

    Google Scholar 

  • Føre M, Dempster T, Alfredsen JA, Johansen V, Johansson D (2009) Modelling of Atlantic salmon (Salmo salar L.) behaviour in sea-cages: A Lagrangian approach. Aquaculture 288:196–204

    Google Scholar 

  • Fritsche R, Nilsson S (1989) Cardiovascular responses to hypoxia in the Atlantic cod, Gadus morhua. J Exp Biol 48:153–160

    CAS  Google Scholar 

  • Fry FEJ (1947) Effects of the environment on animal activity. University of Toronto studies Biological series, No. 55, pp 1–62

    Google Scholar 

  • Fry FEJ (1971) The effect of environmental factors on the physiology of fish. In: Hoar WS, Randall DJ (eds) Fish Physiology, vol 6. Academic Press, New York, pp 1–98

    Google Scholar 

  • Fu SJ, Brauner CJ, Cao ZD, Richards JG, Peng JL, Dhillon R, Wang YX (2011) The effect of acclimation to hypoxia and sustained exercise on subsequent hypoxia tolerance and swimming performance in goldfish (Carassius auratus). J Exp Biol 214:2080–2088

    PubMed  CAS  Google Scholar 

  • Graham JB (1997) Air breathing fishes: evolution, diversity, and adaptation. Academic Press, San Diego

    Google Scholar 

  • Graham JB (2006) Aquatic and aerial respiration. In: Evans DD, Claiborne JB (eds) The physiology of fishes, 3rd edn. CRC Press, Boca Raton, pp 85–117

    Google Scholar 

  • Gray JAB, Denton EJ (1991) Fast pressure pulses and communication between fish. J Mar Biol Assoc UK 71:83–106

    Google Scholar 

  • Green D, McFarland WN (1994) Impact of foraging blacksmiths on constituents in the water column: implications on school behaviour and structure. In Halverson WL, Maender GJ (eds) Proceedings of the 4th California Islands symposium: update on the status of resources.Santa Barbara Museum of Natural History, Santa Barbara, CA, pp 97–102

    Google Scholar 

  • Grigg GC (1965) Studies on the Queensland lungfish, Neoceratodus forsteri (Krefft) III Aerial respiration in relation to habits. Aust J Zool 13:413–421

    Google Scholar 

  • Herbert NA, Steffensen JF (2005) The response of Atlantic cod, Gadus morhua, to progressive hypoxia: fish swimming speed and physiological stress. Mar Biol 147:1403–1412

    Google Scholar 

  • Herbert NA, Steffensen JF (2006) Hypoxia increases the behavioural activity of schooling herring: a response to physiological stress or respiratory distress? Mar Biol 149:1217–1225

    Google Scholar 

  • Herbert NA, Skov PV, Wells RMG, Steffensen JF (2006) Whole blood-oxygen binding properties of four cold-temperate marine fishes: blood-affinity is independent of pH-dependent binding, routine swimming performance and environmental hypoxia. Physiol Biochem Zool 79:909–918

    PubMed  CAS  Google Scholar 

  • Herbert NA, Skjæraasen JE, Nilsen T, Salvanes AG, Steffensen JF (2011) The hypoxia avoidance behaviour of juvenile Atlantic cod (Gadus morhua L.) depends on the provision and pressure level of an O2 refuge. Mar Biol 158:737–746

    Google Scholar 

  • Herskin J, Steffensen JF (1998) Reduced tail beat frequency and oxygen consumption due to hydrodynamic interactions of schooling sea bass, Dicentrarchus labrax L. J Fish Biol 53:366–376

    Google Scholar 

  • Hognestad PT (1994) The Lake Rossfjord herring (Clupea harengus L.) and its environment. ICES J Mar Sci 51:281–292

    Google Scholar 

  • Israeli D, Kimmel E (1996) Monitoring the behavior of hypoxia-stressed Carassius auratus using computer vision. Aquacult Eng 15(6):423–440

    Google Scholar 

  • Jobling M (1994) Fish Bioenergetics. Chapman and Hall, London

    Google Scholar 

  • Johansen JL, Vaknin R, Steffensen JF, Domenici P (2010) Kinematics and energetic benefits of schooling in the labriform fish, striped surfperch Embiotoca lateralis. MEPS 420:221–229

    Google Scholar 

  • Jones DR (1971) The effect of hypoxia and anemia on the swimming performance of rainbow trout (Salmo gairdneri). J Exp Biol 55:541–551

    PubMed  CAS  Google Scholar 

  • Jordan AD, Steffensen JF (2007) The effect of ration size and hypoxia on the specific dynamic action in the cod. Physiol Biochem Zool 80:178–185

    PubMed  Google Scholar 

  • Jourdan-Pineau H, Dupont-Prinet A, Claireaux G, McKenzie DJ (2010) An investigation of metabolic prioritization in the European sea bass, Dicentrarchus labrax. Physiol Biochem Zool 83:68–77

    PubMed  Google Scholar 

  • Keeling RF, Kortzinger A, Gruber N (2010) Ocean deoxygenation in a warming world. Annu Rev Mar Sci 2:199–229

    Google Scholar 

  • Kemp PS, Tsuzaki T, Moser ML (2009) Linking behaviour and performance: intermittent locomotion in a climbing fish. J Zool 277(2):171–178

    Google Scholar 

  • Killen SS, Marras S, Ryan MR, Domenici P, McKenzie DJ (2012a) A relationship between metabolic rate and risk-taking behaviour is revealed during hypoxia in juvenile European sea bass. Funct Ecol. doi:10.1111/j.1365-2435.2011.01920.x

  • Killen SS, Marras S, Steffensen JF, McKenzie DJ (2012b). Aerobic capacity influences the spatial position of individuals within fish schools. Proc R Soc B. doi:10.1098/rspb.2011.1006

  • Kramer DL (1987) Dissolved oxygen and fish behaviour. Environ Biol Fish 18:81–92

    Google Scholar 

  • Kramer DL, Manley D, Bourgeois R (1983) The effect of respiratory mode and oxygen concentration on the risk of aerial predation in fishes. Can J Zool 61:653–665

    Google Scholar 

  • Kramer DL, Rangeley RW, Chapman LJ (1997) Habitat selection: patterns of spatial distribution from behavioural decisions. In Godin JGJ (ed) Behavioural ecology of teleost fishes. Oxford University Press, Oxford, pp 37–80

    Google Scholar 

  • Krause J (1993) The relationship between foraging and shoal position in a mixed shoal of roach (Rutilus rutilis) and chub (Leuciscus cephalus)—a field study. Oecologia 93(3):356–359

    Google Scholar 

  • Krause J, Ruxton GD (2002) Living in groups. Oxford University Press, Oxford

    Google Scholar 

  • Krause J, Reeves P, Hoare D (1998) Positioning behaviour in roach shoals: the role of body length and nutritional state. Behaviour 135:1031–1039

    Google Scholar 

  • Kutty MN (1968) Influence of ambient oxygen on the swimming performance of goldfish and rainbow trout. Can J Zool 46:647–653

    PubMed  CAS  Google Scholar 

  • Lefevre S, Huong DTT, Kim NT, Wang T, Phuong NT, Bayley M (2011) A telemetry study of swimming depth and oxygen level in a Pangasius pond in the Mekong Delta. Aquaculture 315:410–413

    Google Scholar 

  • Lefrançois C, Claireaux G (2003) Influence of ambient oxygenation and temperature on metabolic scope and scope for heart rate of the sole (Solea solea). Mar Ecol Prog Ser 259:273–284

    Google Scholar 

  • Lefrançois C, Domenici P (2006) Locomotor kinematics and responsiveness in the escape behaviour of European sea bass (Dicentrarchus labrax) exposed to hypoxia. Mar Biol 149:969–977

    Google Scholar 

  • Lefrançois C, Shingles A, Domenici P (2005) The effect of hypoxia on locomotor performance and behaviour during escape in the golden grey mullet (Liza aurata). J Fish Biol 67:1711–1729

    Google Scholar 

  • Lefrançois C, Ferrari RS, da Silva JM, Domenici P (2009) The effect of progressive hypoxia on spontaneous activity in single and shoaling golden grey mullet Liza aurata. J Fish Biol 75:1615–1625

    PubMed  Google Scholar 

  • Lowe TE, Brill RW, Cousins KL (2000) Blood oxygen-binding characteristics of bigeye tuna (Thunnus obesus), a high-energy-demand teleost that is tolerant of low ambient oxygen. Mar Biol 136:1087–1098

    Google Scholar 

  • Mallekh R, Lagardère JP (2002) Effect of temperature and dissolved oxygen concentration on the metabolic rate of the turbot and the relationship between metabolic scope and feeding demand. J Fish Biol 60(5):1105–1115

    Google Scholar 

  • McFarland WN, Moss SA (1967) Internal behavior in fish schools. Science 156:260–262

    PubMed  CAS  Google Scholar 

  • McKenzie DJ, Claireaux G (2010) Effects of environmental factors on the physiology of sustained aerobic exercise. In: Domenici P, Kapoor BG (eds) Fish Locomotion—an etho-ecological perspective. Science Publishers, New Hampshire, pp 296–332

    Google Scholar 

  • McKenzie DJ, Steffensen JF, Taylor EW, Abe AS (2012) The contribution of air-breathing to aerobic scope and exercise performance in the banded knifefish Gymnotus carapo L. J Exp Biol 215:1323–1330

    PubMed  Google Scholar 

  • Metcalfe JD, Butler PJ (1984) Changes in activity and ventilation in response to hypoxia in unrestrained, unoperated dogfish (Scyliorhinus canicula L.). J Exp Biol 180:153–162

    Google Scholar 

  • Milligan CL, Hooke GB, Johnson C (2000) Sustained swimming at low velocity following a bout of exhaustive exercise enhances metabolic recovery in rainbow trout. J Exp Biol 203:921–926

    PubMed  CAS  Google Scholar 

  • Moss SA, McFarland WN (1970) Influence of dissolved oxygen and carbon dioxide on fish schooling behavior. Mar Biol 5:100–107

    Google Scholar 

  • Neuenfeldt S, Andersen KH, Hinrichsen H-H (2009) Some Atlantic cod Gadus morhua in the Baltic Sea visit hypoxic water briefly but often. J Fish Biol 75(1):290–294

    PubMed  CAS  Google Scholar 

  • Nilsson GE, Rosen P, Johansson D (1993) Anoxic depression of spontaneous locomotor activity in crucian carp quantified by a computerized imaging technique. J Exp Biol 180:153–162

    Google Scholar 

  • Oppedal F, Dempster T, Stien LH (2011) Environmental drivers of Atlantic salmon behaviour in sea-cages: a review. Aquaculture 311:1–18

    Google Scholar 

  • Partridge BL, Pitcher TJ (1980) The sensory basis of fish schools: relative roles of lateral line and vision. J Comp Physiol 135:315–325

    Google Scholar 

  • Petersen CL (1987) Energy budgets for juvenile rainbow trout at various oxygen concentrations. Aquaculture 62:289–298

    Google Scholar 

  • Petersen LH, Gamperl AK (2010) Effect of acute and chronic hypoxia on the swimming performance, metabolic capacity and cardiac function of Atlantic cod (Gadus morhua). J Exp Biol 213:808–819

    PubMed  CAS  Google Scholar 

  • Pichavant K, Person-Le-Ruyet J, Le Bayon N, Sévère A, Le Roux A, Quémerer L, Maxime V, Nonotte G, Bœuf G (2000) Effects of hypoxia on growth and metabolism of juvenile turbot. Aquaculture 188:103–104

    Google Scholar 

  • Pitcher TJ, Partridge BL (1979) Fish school density and volume. Mar Biol 54:383–394

    Google Scholar 

  • Pitcher TJ, Wyche CJ, Magurran AE (1982) Evidence for position preferences in schooling mackerel. Anim Behav 30:932–934

    Google Scholar 

  • Plante S, Chabot D, Dutil JD (1998) Hypoxia tolerance in Atlantic cod. J Fish Biol 53:1342–1356

    Google Scholar 

  • Poulsen SB, Jensen LF, Nielsen KS, Malte H, Aarestrup K, Svendsen JC (2011) Behaviour of rainbow trout Oncorhynchus mykiss presented with a choice of normoxia and stepwise progressive hypoxia. J Fish Biol 79(4):969–979

    PubMed  CAS  Google Scholar 

  • Randall D (1982) The control of respiration and circulation in fish during exercise and hypoxia. J Exp Biol 100:275–288

    Google Scholar 

  • Randall DJ, Burggren WW, Farrell AP, Haswell MS (1981) The evolution of air-breathing in vertebrates. Cambridge University Press, Cambridge

    Google Scholar 

  • Richards JG (2009) Metabolic and molecular responses of fish to hypoxia. In: Richards JG, Farrell AP, Brauner CJ (eds) Hypoxia. Elsevier, London, pp 443–485

    Google Scholar 

  • Richards JG, Heigenhauser GJF, Wood CM (2002) Lipid oxidation fuels recovery from exhaustive exercise in white muscle of rainbow trout. Am J Physiol 282:R89–R99

    CAS  Google Scholar 

  • Robb T, Abrahams MV (2002) The influence of hypoxia on risk of predation and habitat choice by the fathead minnow, Pimephales promelas. Behav Ecol Sociobiol 52:25–30

    Google Scholar 

  • Rosa R, Seibel BA (2008) Synergistic effects of climate-related variables suggest future physiological impairment in a top oceanic predator. PNAS 105(52):20776–20780

    PubMed  CAS  Google Scholar 

  • Schurmann H, Steffensen JF (1994) Spontaneous swimming activity of Atlantic cod Gadus morhua exposed to graded hypoxia at three temperatures. J Exp Biol 197:129–142

    PubMed  Google Scholar 

  • Schurmann H, Steffensen JF (1997) Effects of temperature, hypoxia and activity on the metabolism of juvenile Atlantic cod. J Fish Biol 50:1166–1180

    Google Scholar 

  • Seymour RS, Christian K, Bennett MB, Baldwin J, Wells RMG, Baudinette RV (2004) Partitioning of respiration between the gills and air-breathing organ in response to aquatic hypoxia and exercise in the Pacific tarpon, Megalops cyprinoides. Physiol Biochem Zool 77:760–767

    PubMed  CAS  Google Scholar 

  • Seymour RS, Farrell AP, Christian K, Clark TD, Bennett MB, Wells RMG, Baldwin J (2007) Continuous measurement of oxygen tensions in the air-breathing organ of Pacific tarpon (Megalops cyprinoides) in relation to aquatic hypoxia and exercise. J Comp Physiol B 177:579–587

    PubMed  CAS  Google Scholar 

  • Shimps EL, Rice JA, Osborne JA (2005) Hypoxia tolerance in two juvenile estuary dependent fishes. J Exp Mar Biol Ecol 325:146–162

    Google Scholar 

  • Shingles A, McKenzie DJ, Claireaux G, Domenici P (2005) Reflex cardioventilatory responses to hypoxia in the flathead grey mullet (Mugil cephalus) and their behavioural modulation by perceived threat of predation and water turbidity. Physiol Biochem Zool 78:744–755

    PubMed  CAS  Google Scholar 

  • Shoji J, Masuda R, Yamashita Y, Tanaka M (2005) Effect of low dissolved oxygen concentrations on behavior and predation rates on red sea bream Pagrus major larvae by the jellyfish Aurelia aurita and by juvenile Spanish mackerel Scomberomorus niphonius. Mar Biol 147:863–868

    Google Scholar 

  • Smatresk NJ (1990) Chemoreceptor modulation of the endogenous respiratory rhythm in vertebrates. Am J Physiol 259:887–897

    Google Scholar 

  • Smith KJ, Able KW (2003) Dissolved oxygen dynamics in salt marsh pools and its potential impacts on fish assemblages. Mar Ecol Prog Ser 258:223–232

    CAS  Google Scholar 

  • Smith RS, Kramer DL (1986) The effect of apparent predation risk on the respiratory behavior of the Florida gar (Lepisosteus platyrhincus). Can J Zool 64:2133–2136

    Google Scholar 

  • Sollid J, Nilsson GE (2006) Plasticity of respiratory structures-adaptive remodeling of fish gills induced by ambient oxygen and temperature. Respir Physiol Neurobiol 154:241–251

    PubMed  CAS  Google Scholar 

  • Steffensen JF (1995) Possible limitations of speed and size of swimming fish schools, based on oxygen consumption of herring, Clupea harengus, measured at different swimming speeds. J Physiol 483:192

    Google Scholar 

  • Stierhoff KL, Targett TE, Power JH (2009) Hypoxia-induced growth limitation of juvenile fishes in an estuarine nursery: assessment of small-scale temporal dynamics using RNA:DNA. Can J Fish Aquat Sci 66:1033–1047

    CAS  Google Scholar 

  • Stramma L, Prince ED, Schmidtko S, Jiangang L, Hoolihan JP, Visbeck M, Wallace DWR, Brandt P, Körtzinger A (2012) Expansion of oxygen minimum zones may reduce available habitat for tropical pelagic fishes Nature. Clim Change 2:33–37

    CAS  Google Scholar 

  • Svendsen JC, Steffensen JF, Aarestrup K, Frisk M, Etzerodt A, Jyde M (2012) Excess posthypoxic oxygen consumption in rainbow trout (Oncorhynchus mykiss): recovery in normoxia and hypoxia. Can J Zool 90:1–11

    CAS  Google Scholar 

  • Taylor JC, Miller JM (2001) Physiological performance of juvenile southern flounder, Paralichthys lethostigma (Jordan and Gilbert 1884), in chronic and episodic hypoxia. J Exp Mar Biol Ecol 258(2):195–214

    PubMed  Google Scholar 

  • Thetmeyer H, Waller U, Black KD, Inselmann S, Rosenthal H (1999) Growth of European sea bass Dicentrarchus labrax L. under hypoxic and oscillating oxygen condition. Aquaculture 174:355–367

    Google Scholar 

  • Vagner M, Lefrancois C, Ferrari RS, Satta A, Domenici P (2008) The effect of acute hypoxia on swimming stamina at optimal swimming speed in flathead grey mullet Mugil cephalus. Mar Biol 155(2):183–190

    Google Scholar 

  • Walker JA, Ghalambor CK, Griset OL, Kenney DM, Reznick DN (2005) Do faster starts increase the probability of evading predators? Funct Ecol 19:808–815

    Google Scholar 

  • Webb PW (1998) Swimming. In: Evans DD (ed) The physiology of fishes, 2nd edn. CRC Press, Boca Raton, pp 3–24

    Google Scholar 

  • Weihs D (1973) Hydromechanics and fish schooling. Nature 241:290–291

    Google Scholar 

  • Weihs D (1974) Energetic advantages of burst swimming of fish. J Theor Biol 48(1):215–229

    PubMed  CAS  Google Scholar 

  • Wood CM (1991) Acid-base and ion balance, metabolism, and their interactions, after exhaustive exercise in fish. J Exp Biol 160:285–308

    CAS  Google Scholar 

  • Zhang W, Cao ZD, Peng JL, Chen BJ, Fu SJ (2010) The effects of dissolved oxygen level on the metabolic interaction between digestion and locomotion in juvenile southern catfish (Silurus meridionalis Chen). Comp Biochem Physiol 157A:212–219

    CAS  Google Scholar 

Download references

Acknowledgements

PD received funding from the European Community's Seventh Framework Programme (FP7/2007-2013) under Grant Agreement No. 266445 for the project Vectors of Change in Oceans and Seas Marine Life, Impact on Economic Sectors (VECTORS).

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to P. Domenici .

Editor information

Editors and Affiliations

Rights and permissions

Reprints and permissions

Copyright information

© 2013 Springer-Verlag Berlin Heidelberg

About this chapter

Cite this chapter

Domenici, P., Herbert, N.A., Lefrançois, C., Steffensen, J.F., McKenzie, D.J. (2013). The Effect of Hypoxia on Fish Swimming Performance and Behaviour. In: Palstra, A., Planas, J. (eds) Swimming Physiology of Fish. Springer, Berlin, Heidelberg. https://doi.org/10.1007/978-3-642-31049-2_6

Download citation

Publish with us

Policies and ethics