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B. García (1994)
Factores que influyen sobre el consumo de oxígeno, ingesta y crecimiento en la dorada leparus surata L.J : una aproximación al establecimiento de modelos lineales / Benjamín García García ; director Salvador Zamora Navarro
R. Weiss (1970)
The solubility of nitrogen, oxygen and argon in water and seawaterDeep Sea Research and Oceanographic Abstracts, 17
J. Steffensen, J. Lomholt, K. Johansen (1982)
Gill ventilation and O2 extraction during graded hypoxia in two ecologically distinct species of flatfish, the flounder (Platichthys flesus) and the plaice (Pleuronectes platessa)Environmental Biology of Fishes, 7
Ott Ott, Heisler Heisler, Ultsch Ultsch (1980)
A re‐evaluation of the relationship between temperature and the critical oxygen tension in freshwater fishesComp. Biochem. Physiol., 67A
V. Maxime, K. Pichavant, G. Boeuf, G. Nonnotte (2004)
Effects of hypoxia on respiratory physiology of turbot, Scophthalmus maximusFish Physiology and Biochemistry, 22
Hughes Gm, Saunders Rl (1970)
Responses of the respiratory pumps to hypoxia in the rainbow trout (Salmo gairdneri).The Journal of Experimental Biology, 53
M. Jobling (1982)
A study of some factors affecting rates of oxygen consumption of plaice, Pleuronectes platessa L.Journal of Fish Biology, 20
A. Kalinin, F. Rantin, M. Glass (1993)
Dependence on body size of respiratory function in Hoplias malabaricus (Teleostei, Erythrinidae) during graded hypoxiaFish Physiology and Biochemistry, 12
J. Valverde (2002)
Factores que afectan al consumo de oxígeno, concentraciones crítica y letal de oxígeno, y frecuencia de ventilación en el sargo picudo (diplodus puntazzo), el dentón común (dentex dentex) y el pulpo de roca (octopus vulgaris)
Maxime Maxime, Pichavant Pichavant, Boeuf Boeuf, Nonnote Nonnote (2000)
Effects of hypoxia on respiratory of turbot, Scophthalmus maximusFish Physiol. Biochem., 22
M. Hernández, M. Egea, F. Rueda, F. Aguado, F. Martínez, B. García (2001)
Effects of commercial diets with different P/E ratios on sharpsnout seabream (Diplodus puntazzo) growth and nutrient utilizationAquaculture, 195
Alzieu C. (1991)
3
M. Fernandes, F. Rantin (1989)
Respiratory responses of Oreochromis niloticus (Pisces, Cichlidae) to environmental hypoxia under different thermal conditionsJournal of Fish Biology, 35
H. Schurmann, J. Steffensen (1992)
Lethal oxygen levels at different temperatures and the preferred temperature during hypoxia of the Atlantic cod, Gadus morhua L.Journal of Fish Biology, 41
F. Rantin, A. Kalinin, M. Glass, M. Fernandes (1992)
Respiratory responses to hypoxia in relation to mode of life of two erythrinid species (Hoplias malabaricus and Hoplias lacerdae)Journal of Fish Biology, 41
D. Randall (1982)
The Control of Respiration and Circulation in Fish During Exercise and HypoxiaThe Journal of Experimental Biology, 100
Secor Secor, Gunderson Gunderson (1998)
Effects of hypoxia and temperature on survival, growth, and respiration of juvenile Atlantic sturgeon, Acipenser oxyrinchusFish. Bull., 96
L. Cariello, B. Salvato, G. Jori (1980)
Partial characterization of suberitine, the neurotoxic protein purified from Suberites domunculaComparative Biochemistry and Physiology B, 67
D. Chabot, J. Dutil (1999)
Reduced growth of Atlantic cod in non‐lethal hypoxic conditionsJournal of Fish Biology, 55
H. Schurmann, J. Steffensen (1997)
Effects of temperature, hypoxia and activity on the metabolism of juvenile Atlantic codJournal of Fish Biology, 50
D. Jones (1971)
Theoretical analysis of factors which may limit the maximum oxygen uptake of fish: the oxygen cost of the cardiac and branchial pumps.Journal of theoretical biology, 32 2
Summary The respiratory behaviour of the sharpsnout sea bream (Diplodus puntazzo) with fish weights between 15 and 509 g at temperatures of 15–29°C was studied, with special attention paid to critical and lethal oxygen saturation (Scrit and LC50, respectively) and ventilatory frequency (Vf). The species maintained a constant oxygen consumption rate regardless of the concentration of dissolved oxygen, until Scrit was reached. The mean of Scrit and LC50 was 34% (2.4 mg L−1) and 11% (0.8 mg L−1), respectively. The Scrit was independent of fish weight and temperature, whereas the LC50 values were positively correlated with both factors (P < 0.05). The higher resistance in small fish could be due to their greater Vf response to hypoxia than in larger animals. Furthermore, the increased metabolism resulting from the effect of temperature was offset by an increased Vf. The Vf remained constant down to a mean value of 67% oxygen saturation, regardless of fish weight and temperature. These findings suggest an optimum oxygen saturation of above 70% for D. puntazzo culture.
Journal of Applied Ichthyology – Wiley
Published: Dec 1, 2004
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