The effect of salinity change on the oxygen consumption and swimming activity of the high-shore rockpool copepod Tigriopus brevicornis

2001 ◽  
Vol 263 (2) ◽  
pp. 227-240 ◽  
Author(s):  
Rob McAllen ◽  
Alan Taylor
Author(s):  
G. S. Preece

High- and low-shore populations of Bathyporeia pilosa LindstrÖm, kept in the laboratory under natural day-night illumination and constant dark conditions, show distinct swimming rhythms of tidal frequency (12–4 h) with activity maxima on the early ebb tide. A diurnal component is evident, activity during thenight being greater than during the day. The tidal rhythm deteriorates under laboratory conditions, but swimming activity recurs after a semi-lunar period. Under natural illumination, both populations show a night tide swimming rhythm of semi-lunar frequency, activity occurring mainly over the 'falling' spring tides. Plankton sampling on night tides over the area of the beach occupied by high-shore B. pilosa shows that the animals emerge and swim on ebb tides which are in phase with darkness. The importance of exogenous factors such as wave action, pressure, temperature and light is discussed. Ecological implications and the possible function of the swimming rhythm are considered.


Parasitology ◽  
2000 ◽  
Vol 121 (1) ◽  
pp. 75-83 ◽  
Author(s):  
K. NIMETH ◽  
P. ZWERGER ◽  
J. WÜRTZ ◽  
W. SALVENMOSER ◽  
B. PELSTER

The ability of the nematode Anguillicola crassus to infect eel larvae (glass-eel stage) was tested. The results show that glass-eels fed on infected copepods, the natural intermediate host of the nematode, can be infected. Light microscopical examination of the infected developing swimbladder tissue revealed that the infection results in a significant thickening of the connective tissue. The basolateral labyrinth of gas gland cells is very much reduced in infected swimbladders, and the distance of gas gland cells to blood capillaries is enlarged. Critical swimming speed, defined as the speed where the larvae were no longer able to swim against the current, was similar in infected and uninfected animals. At intermediate speeds (about 60–80% of critical swimming speed) infected eels showed a slightly higher swimming activity than control animals. Resting oxygen consumption, measured as an index of metabolic activity, within the first 2 months of infection was higher in control animals, which may be due to a reduced rate of activity in infected glass-eels. By 4–5 months after the infection, however, it was significantly higher in infected animals. This may indicate that at this stage a higher activity of the animals is required to compensate for the increase in body density, but swimming performance of infected and non-infected glass-eels was not significantly different. Oxygen consumption during swimming activity, measured in a swim tunnel at 50% of maximal swimming speed, also was not affected. The results thus show that even glass-eels can be infected with A. crassus, and this probably contributes to the rapid spread of the nematode in Europe. While aerobic metabolism during swimming activity is not affected at this stage of infection, the swimbladder tissue shows severe histological changes, which most likely will impair swimbladder function.


1982 ◽  
Vol 97 (1) ◽  
pp. 359-373 ◽  
Author(s):  
G. G. Duthie

(1) The standard oxygen consumption and the oxygen consumption during measured swimming activity have been determined in three flatfish species at 5, 10 and 15 degrees C. (2) The relationship between weight and standard oxygen consumption for flatfish conform to the general relationship Y = aWb. On an interspecies basis, standard oxygen consumption of flatfish is significantly lower than that of roundfish. (3) A semilogarithmic model describes the relationship between oxygen consumption and swimming speed for the three species. Values for maximum oxygen consumption, metabolic scopes and critical swimming speeds are low in comparison to salmonids. (4) The optimum swimming speeds and critical swimming speeds of flatfish are similar. It is suggested that, over long distances, flatfish adopt a strategy of swimming at supercritical speeds with periods of intermittent rest to repay the accrued oxygen debt. (5) Elevated lactic acid levels in flounder white muscle after moderate swimming indicate an additional 15% anaerobic contribution to the cost of locomotion as calculated from aerobic considerations.


1968 ◽  
Vol 25 (12) ◽  
pp. 2603-2608 ◽  
Author(s):  
J. S. Hart

The respiratory metabolism of groups of goldeye was measured during rest and sustained swimming activity at 5, 10, and 15 C under conditions of continuous reduction in oxygen by the metabolism of the fish. The oxygen consumption fell progressively during swimming at all temperatures indicating dependence of metabolism on oxygen supply at all pO2 levels. During rest the oxygen consumption was relatively independent of pO2 until certain critical levels were reached. Respiration became markedly limited by CO2 in the medium when the pCO2 exceeded 50 mm Hg. It is apparent that survival possibilities of goldeye would be limited by pO2 and pCO2 between 20–40 mm Hg during the winter.


2007 ◽  
Vol 50 (1) ◽  
pp. 101-112 ◽  
Author(s):  
Edison Barbieri

This study aimed to investigate the toxicological effects of the LAS-C12 on Mugil platanus (mullet). Fishes exposed to 1.0 mg.L-1 for 24, 48, 72, 96 and 120 hours presented significant increase in specific routine metabolism. At the concentration of 0.5 mgL-1, the active metabolism presented a decreasing trend from 48 h of exposure on. However, only the consumption averages for 72 h were statistically different from the ones obtained for other periods of exposure. The lowest oxygen consumption in this concentration was observed for 24, 48 and 72 hours of exposure. Significant differences between the control and the concentration of 2.5 mgL-1 were observed for the different periods of exposure. It was not possible to measure the consumption of oxygen for 96 and 120 h, because the fishes got tired in less than one minute after they were placed in the respirometer. The time of swimming until exhausted for fish exposed to 2.5 mgL-1 of LAS-C12 for 24 h was 8 minutes. Following 72 hours of exposure to this concentration, the fish got exhausted after 3 minutes.


1972 ◽  
Vol 29 (1) ◽  
pp. 67-77 ◽  
Author(s):  
B. S. Muir ◽  
A. J. Niimi

Active and standard metabolism of Kuhlia sandvicensis increase with fish weight to a power of about 0.8 and active is nine times standard. No significant difference was found between experiments in fresh water and 30‰ sea water at 23 C. At low swimming speeds the fish may be unable to physically take up as much oxygen as at higher speeds. Swimming activity may be essential to circulatory adequacy.Elevated oxygen consumption lasted for 42 hr following a ration of 2.3% of body weight and for 60 hr after one of 4.5%. It amounted to about 76 mg O2/g ration, equivalent to about 16% of the energy of the ration, in both cases. For a nonswimming fish the highest oxygen consumption observed following the maximum daily ration is no more than half of the difference between active and standard rates.


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