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The validity of using extruded intra-ovarian oocytes for in vivo assessment of ovarian maturity in the grey mullet was established. The diameter of sampled, unfixed oocytes was used as a reference point for comparative purposes. Analysis of variations in oocyte diameters among samples removed from seven different ovarian locations indicated that mullet oocytes develop in synchrony and that in vivo samples taken from any area in the ovary would be representative of the entire ovary. Statistical analyses of oocyte diameters and diameter-frequency distributions data from duplicate in vivo samples removed from the same ovarian site in each of 17 females showed no significant differences and validated the accuracy of the method. Similar comparisons of data from in vivo and in vitro samples revealed no statistically significant differences.

Larvae from artificially bred grey mullet were reared in the laboratory and survival rates of 0.2 %, 5 % and 5 % achieved in three of six trials. Food consisted of wild zooplankton and Artemia nauplii. Feeding began on the fifth day, when the yolk sac was depleted, and intensified on the ninth day. The rate of yolk absorption and feeding intensity were reflected in the growth curve. Larval survival was not affected by withholding food from the larvae till the seventh day from hatching. Two critical periods associated with high larval mortality were apparent on the 2nd-3rd and 8th-11 th days after hatching. These were preceded by an increase in specific gravity of larvae followed by passive sinking to the bottom of the rearing tank. Larval length increased from 2 6 3 mm at hatching to 1769 mm at the end of the 42-day larval period. The larvae survived on benthic diatoms therefter. Maximum survival rates were achieved at 22" C. (Oceanic Institute Contribution No. 101).

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