Variation in the food intake of grass carp, Ctenopharyngodon idella (Val.), fed singly or in groups

Each animal may be assumed to possess a unique combination of physiological traits (Bennett, 1987). However, there is little information on thc effects of interindividual variation in fish (Cui and Liu, 1990). Individual differences in competitive ability, aggressiveness and or size can lead to the establishment of dominance hierarchies within groups of fish (Metcalfe, 1989; Metcalfe et al., 1989). The variation in growth rates in groups of fish are rclated to dominance hierarchies and preferential access to food resources by dominant individuals (Jenkins, 1969; Fausch, 1984; Koebele, 1985). Recently, radiography has been used to measure individual consumption rates for groups of salmonids and has demonstrated considerable inter-individual variation in food intake (Jobling et al., 1989; Carter et al., 1992a; McCarthy et al., 1992). Two aims of this study were to use radiography to examine the variation in the food consumption rate of grass carp, Ctenopharyngodon idellu (Val.), held together and to assess whcther variation in growth rates could bc explained by variation in consumption rates. A final aim of this study was to compare the day to day variation in consumption rates of grass carp held in a group to thosc held individually, in terms of the individual meal share, in order to examine the cffect of endogenous influences on appetite

Swimming physiology of European silver eels (Anguilla anguilla L.): energetic costs and effects on sexual maturation and reproduction

The European eel migrates 5,000–6,000 km to the Sargasso Sea to reproduce. Because they venture into the ocean in a pre-pubertal state and reproduce after swimming for months, a strong interaction between swimming and sexual maturation is expected. Many swimming trials have been performed in 22 swim tunnels to elucidate their performance and the impact on maturation. European eels are able to swim long distances at a cost of 10–12 mg fat/km which is 4–6 times more efficient than salmonids. The total energy costs of reproduction correspond to 67% of the fat stores. During long distance swimming, the body composition stays the same showing that energy consumption calculations cannot be based on fat alone but need to be compensated for protein oxidation. The optimal swimming speed is 0.61–0.67 m s−1, which is ~60% higher than the generally assumed cruise speed of 0.4 m s−1 and implies that female eels may reach the Sargasso Sea within 3.5 months instead of the assumed 6 months. Swimming trials showed lipid deposition and oocyte growth, which are the first steps of sexual maturation. To investigate effects of oceanic migration on maturation, we simulated group-wise migration in a large swim-gutter with seawater. These trials showed suppressed gonadotropin expression and vitellogenesis in females, while in contrast continued sexual maturation was observed in silver males. The induction of lipid deposition in the oocytes and the inhibition of vitellogenesis by swimming in females suggest a natural sequence of events quite different from artificial maturation protocols