Fecundity, Spawning, and Maturity of Female Dover Sole, Microstomus Pacificus, with an Evaluation of Assumptions and Precision

Southwest Fisheries Science Center, National Marine Fisheries Service, NOAA P.O. Box 271, La Jolla, California 92038 Fecundity, spawning, and maturity of female Dover sale Microstomus pacificus, with an evaluation of assumptions and precision Abstract.-The potential annual fecundity of Dover sole becomes fixed before the spawning season when the average diameter of the advanced stock of yolked oocytes exceeds 0.86 mm; hence potential annual fecundity is determinate. More central California females had atretic advanced oocytes than Oregon females, but rates of atresia were not sufficiently high to have an important effect on the potential annual fecundity of the population. A I-kg female matured about 83,000 advanced yolked oocytes at the beginning .of the season. Vitellogenesis continued for the advanced yolked oocytes during most of the spawning season while batches were repetitively matured and spawned. About nine batches were spawned over a six-month spawning season (December-May), and spawning ceased when the standing stock of advanced oocytes was exhausted. A I-kg female released about 10,000 eggs per spawning, except for the first and last batches which were smaller than the rest. Near the end of the season, females may spawn more frequently than earlier in the year, increasing the daily production of eggs by the population even though fewer females are reproductively active. Annual reproductive effort of Dover sole was equivalent to about 14% of body wet weight per year. Fifty percent of the females had become sexually mature when they reached 332mm total length. Various methodological issues were also treated in this paper, including validation of key assumptions underlying estimates of annual fecundity; fecundity sample-size requirements; evaluation of criteria and bias in estimating female sexual maturity; and comparisons of classification by histology and gross anatomy.

[1]  J. Hunter,et al.  FECUNDITY AND OTHER ASPECTS OF THE REPRODUCTION OF SABLEFISH, ANOPLOPOMA FIMBRIA, IN CENTRAL CALIFORNIA WATERS , 1989 .

[2]  D. Gunderson,et al.  Reproductive effort as a predictor of natural mortality rate , 1988 .

[3]  J. Lambert,et al.  The ovary of the Guppy, Poecilia reticulata , 1970, Zeitschrift für Zellforschung und Mikroskopische Anatomie.

[4]  J. Hunter,et al.  Measurement of Spawning Frequency in Multiple Spawning Fishes , 2004 .

[5]  D. Kimura,et al.  Mixtures of Empirical Distributions: An Iterative Application of the Age- Length Key , 1987 .

[6]  J. Alheit Reproductive biology of sprat (Sprattus sprattus): Factors determining annual egg production , 1986 .

[7]  L. Bretschneider,et al.  Sexual Endocrinology of Non-Mammalian Vertebrates , 1948 .

[8]  J. Hunter,et al.  BATHYMETRIC PATTERNS IN SIZE, AGE, SEXUAL MATURITY, WATER CONTENT, AND CALORIC DENSITY OF DOVER SOLE, MICROSTOMUS PACIFICUS , 1990 .

[9]  J. Hjort REPORT ON HERRING-INVESTIGATIONS UNTIL JANUARY 1910 , 1910 .

[10]  Vernon M. Chinchilli,et al.  An Asymptotic Confidence Region for the ED 100p From the Logistic Response Surface for a Combination of Agents , 1986 .

[11]  Charles C. Thigpen,et al.  A Sample-Size Problem in Simple Linear Regression , 1987 .

[12]  J. Horwood,et al.  Determinacy of fecundity in sole (Solea solea) from the Bristol Channel , 1990, Journal of the Marine Biological Association of the United Kingdom.

[13]  Keith,et al.  STOCHASTIC AGE-FREQUENCY ESTIMATION USING THE VON BERTALANFFY GROWTH EQUATION , 2004 .

[14]  Stephen R. Goldberg,et al.  SPAWNING INCIDENCE AND BATCH FECUNDITY IN NORTHERN ANCHOVY, ENGRAULIS MORDAX 1 , 1980 .