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  • 1
    ISSN: 1432-136X
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Summary 1. The rates of oxygen consumption ( $$\dot V_{{\text{O}}_2 } $$ ) of individual crabs varied with their live mass. Mean $$\dot V_{{\text{O}}_2 } $$ increased with acclimation temperature in 100% seawater (Q10 2.36) but not in 50% seawater. 2. Exposure to 50% seawater caused a significant increase in $$\dot V_{{\text{O}}_2 } $$ to twice the rate in 100% seawater at 10°C. There was no significant increase in $$\dot V_{{\text{O}}_2 } $$ on dilution at 18°C (Fig. 5). 3. Heart rate, ventilation volume ( $$\dot V$$ ) and a-VO 2 content difference were unaffected by dilution. The rise in $$\dot V_{{\text{O}}_2 } $$ , following dilution at 10°C may, as far as the cardiovascular system is concerned, arise from an increase in cardiac stroke volume. 4. Crabs were isosmotic with 100% seawater at 10°C, 14°C and 18°C. In 50% seawater all crabs showed a significant reduction in blood osmolarity, though they maintained the ΔF.p. and Na+ concentration significantly above that of the medium. Crabs acclimated to 10°C maintained a significantly higher blood ΔF.p. and Na+ concentration in 50% seawater than crabs at 18°C (Fig. 6). 5. Crabs acclimated to 10°C were significantly more active after exposure to 50% seawater. There was no significant change in activity, following dilution, in crabs at 18°C (Fig. 7). 6. The variations in $$\dot V_{{\text{O}}_2 } $$ with temperature and salinity seem to relate to the measured changes in patterns of osmoregulation and activity. At 10°CCarcinus osmoregulates more effectively than at 18°C and is hyperactive in low salinities, which may represent an avoidance reaction. At 18°C, the summer temperature, the crab tolerates internal dilution and is relatively quiescent.
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  • 2
    ISSN: 1432-136X
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Summary 1. TheP IO2 at which crabs emerged from shallow seawater during progressive hypoxia (Table 1), as well as theP c levels for $$\dot V_{O_2 }$$ (Fig. 2) and $$\dot V_g $$ (Fig. 4) of submerged crabs, increased with acclimation temperature and following exposure to 50% seawater at low temperatures (Fig. 6). This pattern of variation resembles the changes in relative oxygen demand with temperature and salinity. 2. TheP c levels for heart rate increased with acclimation temperature but were unaffected by dilution (Fig. 6). 3. Percentage extraction of oxygen from the respired water (Table 2) as well as the levels of motor activity (Fig. 5) were not affected by exposure to hypoxia. 4. Lactic acid concentration in the blood of submerged crabs increased markedly during hypoxia and there was an enhanced $$\dot V_{O_2 }$$ on recovery in normoxia (Fig. 2), which apparently served to completely repay an accumulated oxygen debt. 5. It was concluded that when exposed to environmental hypoxiaCarcinus can adopt the alternative strategies of either accumulating an oxygen debt when in deep water or emerging into air from shallow water to aerate the branchial chambers.
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