S. galilaeus was sampled from a small concrete pond (internal measurements, 6.3.X 1.4 X 1.6 m) at the Institute of Aquatic Biology in Ghana.

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' Aquacultiu-e. 25 (1981) 95 99 Elsevier Scientific Publishing Company, Amsterdam Printed in The Netherlands» Short Communication FECUNDITY AND SPAWNING FREQUENCY OF GAL/LA ENS IN A CONCRETE POND SAROTHERODON JOHN BLAY, JR. Institute of Aquatic Biology (C.S.I.R.), P.O. Box 38, Achimota (Ghana) (Accepted 29 September 1980) ABSTRACT Blay, J., Jr., 1981. Fecundity and spawning frequency ol Sarotherodon galilaeus in a concrete pond. Aquaculture, 25; 95 99. Fecundity of 26 specimens ol Sarolherodon galilaeiis cultured in a small concrete pond, 6.3 X 1.4 X 1.6 m, was determined by the "whole-count" method. The fish were not fed artificially but depended on natural piiytoplankton growth, mainly Chlorococcus and Chlorella, for food. Pond water temperatures varied between 26 and 32 C. Fecundity ranged from 69 to 302 (mean = 149) for fish measuring 6.7 to 11.0 cm total length with 'body weights of 6.2 to 22.3 g and gonad weights of 0.32 to 1.23 g. The relationship between fecundity and total length was non-linear while fecundity body weight and fecundity ovary weight relationships were linear. The frequency distribution of ova diameters in mature ovaries showed two separate modes representing mature and immature ova, suggesting that the species ha.s a restricted spawning period in the pond. INTRODUCTION Tiiapias, including Rarot/jerodo/?, ^a/i/aeus, are known to be prolific breeders and, in captivity, control over their breeding is usually a problem. On the other hand, under hatchery conditions it is often required to produce several thousands of fingerlings to stock production ponds in intensive fish culture. Studies on the fecundity of tiiapias under various culture conditions are therefore essential in estimating their reproductive potential in order to determine the need or otherwise for measures to control their breeding. In Ghana S.. galilaeus promises to be of great value in future tilapia culture in view of its ready availability and abundance in many rivers and lakes in the country. This work aims at contributing to information on the reproductive potential of the species in captivity in small ponds. MATERIALS AND METHODS S. galilaeus was sampled from a small concrete pond (internal measurements, 6.3.X 1.4 X 1.6 m) at the Institute of Aquatic Biology in Ghana. 0044-8486/81/0000-0000/$ 02.50 1981 Elsevier Scientific Publishing Company

96 The water level was maintained at 0.9 rn. The fish liad been cultured and maintained on natural phytoplanktori production of the pond for nearly 3 years, and were not fed on artificial feeds during the sampling period. The main phytoplantons were Chlorococcus and Chlorella. The fish were measured for total and standard lengths to the nearest 0.1 cm and weighed to the nearest 0.1 g. Ripe ovaries were weighed and stored in Gilson's fixative and the eggs separated from the ovarian tissue by frequent vigorous agitation of the specimen bottles after a week. The eggs were cleaned thoroughly by rinsing with the fixative three or four times. The ripe eggs were counted with a tally-counter ("whole-count" method) as they were large and few in number. The sizes of eggs (longest axis) of four mature ovaries were measured with the aid of a dissecting microscope fitted with a micrometer eyepiece, and their frequency distribution plotted. RESULTS Fecundity The fecundity defined by Bagenal and Braum (1968) as the number of ripe ova in the female prior to the next spawning period was determined by counting all mature eggs in the ripe ovary. The fecundity was expressed in relation to the length, body weight and ovary weight. In 26 ripe females, the fecundity varied from 69 to 302 with a mean of 149. This was determined in fish of total lengths 6.7 to 11.0 cm with body weights of 6.2 to 22.3 g and ovary weights of 0.32 to 1.23 g. The fecundity total length relationship (Fig. la) was curvilinear, described by the equation F - 0.7244 L''-'' where F is fecundity and L is total length in centimetres. Fecundity increased rapidly in fish of 8.5 cm length and above. Both fecundity body weight (Fig. lb) and fecundity ovary weight (Fig. Ic) relationships were rectilinear. The former is described by the equation F - 8.89 BW + 23.08 and the latter by the equation F = 193.29 GW- 10.77 where BW and GW are body weight and gonad weight, respectively, in grams. Ova diameter frequency The frequency distribution of ova diameters of four ovaries (Fig. 2) showed two distinct modes of small and large ova. The small ova had a modal diameter of 0.50 mm while the large ova had modal diameters ranging from

97 y "^"'S'" '9l Ovum Diameter XIO "'mrn) Fig. 1. Scatter diagram.s showing relationsliip between (a) fecundity and total length, (b) fecundity and body weight, and (c) fecundity and ovary weight in S. galilaeus. The curve and lines were fitted by the calculated regre,s.sions. n = number of fish; r = correlation coefficient. Fig. 2. The frequency distribution of ova diameters in ripe ovaries of S. galilaeus. TL = total body length; N = number of ova. 2.50 to 2.70 mm. The former are whitish and represent an immature egg stock while the latter are greenish or greenish-brown and represent mature eggs which may he ready to he spawned.

98 DISCUSSION Fish that protect their hrood in one way or another often have a low fecundity because of the presence of some mechanism for ensuring maximum survival of the hrood. Siddiqui (1977), for example, attributes the low fecundity of Tilapia leucosticta in Lake Naivasha, Kenya, to its mouthbrooding habit. Sarotherodon galilaeus is a mouth-brooder in which both males and females participate in the brooding of eggs and fry. The fecundity of the fish in the pond increased with increasing length, body weight and ovary weight (Fig. 1). The presence of ripe ovaries in specimens of 6.7 to 11.0 cm total length indicates that females in this size range me mature. This conforms with the observation of Hickling (1962) that tiiapias in fish ponds mature at a small size, a phenomenon referred to as "stunting". S. galilaeus matures at larger sizes in open environments (Ben-Tuvia, 1959; Lelek and Wuddah, 1968; lies and Holden, 1969) hut no report of mature specimens below 11.0 cm, the maximum length observed for females in this study, had been made. Recently, Blay (in preparation) observed specimens of 9.6 to 11.0 cm total length in the Dawhenya Reservoir, Ghana, with mature ovaries. There are no comparative data on the fecundity of S. galilaeus in the size range encountered in this study. Fecundities of over 500 have been observed (Lowe, 1955; Ben-Tuvia, 1959) in specimens of total length 16.0 cm and above. Extrapolation of fecundity qf specimens of 16.0 cm and longer from the equation, F = 0.7244 L^-^' determined for the fish in this study reveals that if the pond fishes could attain larger sizes, their fecundity would he similar to that of the wild populations. If somatic growth of the fish could he enhanced by supplementary feeding and/or delayed maturation of the gonads, comparable sizes to the wild populations with a corresponding increase in fecundity could he achieved. This would he desirable in the production of large numbers of fry in hatchery practices. Hickling and Rutenherg (1936) interpreted the occurrence of tvm separate groups of eggs in the ovary, one immature and the other mature, as indicative of a short and definite spawning period. Fryer and lies (1972) have observed that tiiapias exhibit protracted spawning, hut the present results indicate a probable restricted spawning period. Studies on the actual spawning behavior of the species in small ponds would he more conclusive in determining its spawning frequency under such conditions. ACKNOWLEDGEMENTS I thank the Institute of Aquatic Biology for the facilities used in this work. My thanks are also due to the Dixector of the Institute, Dr. M.A. Oc'ei, for

99 his useful criticism of the draft manuscript, and to the staff of the Fishery Section of the same Institute for their help. REFERENCES Bagcnal, T.B. and Braum, E., 1968. Egg.s and early life history. In: W.E. Richer (Editor), Methods for Asse.ssment of Fish Production in Freshwater. Biackweli, Oxford, pp. 159-178. Ben-Tuvia, A., 1959. The biology of the cichiid fishes of Lake Tiberias and Huieh. Bull. Res. Counc. Isr., 88 (4): 153-188. Fryer, G. and lies, T.D., 1972. The Cichiid Fishes of the Great Lakes of Africa; their Biology and Evolution. Oliver and Boyd, Edinburgh, 641 Hickiing, C.F,, 1962. Fish Culture. Faber and Faber, London, 295 pp. Hickiing, C.F. and Rutenberg, E., 1936. The ovary as an indicator of spawning period in fishes. J. Mar. Biol. A.ssoc. U.K., 21: 311 317. lies, T.D. and Hoiden, M.J., 1969. Biparental mouth-brooding in Tilapia galilaea (Pisces, Cichlidae). J. Zooh, Lond., 158(3): 327-333. Leiek, A. and Wuddah, A.A., 1968. Contribution to the maturity and fecundity of Tilapia galilaea (Linnaeus) in the Volta Lake. Vestn. Cesk. Zemed. Mus., 32(4): 342-349. Lowe, R.H., 1955. The fecundity of Tiiapia species. East Afr. J., 21(1): 45-52. Siddiqui, A.Q., 1977. Reproductive biology, length weight relationship and relative condition of Tilapia leucosticta (Trewavas) in Lake Naivasha, Kenya. J. Fish. Biol., (1977) 10(3): 251-260. pp.

VOL. 25 NO. 1 AQUACULTURE JULY 1981 CONTENTS t\bstracts/contents list published in: Aquatic Science and Fisheries Abstracts, Biologic Abstracts, Current Contents AB & ES, Freshwater and Aquacuiture Contents Tables) Commercial single-cell proteins either as sole food source or in formulated diets for intensive and continuous production of rotifers {Brachionus piicatiiis) F.-J. Gatesoupe 'Ascain, France) and J.H. Robin (Brest, France) 1 Mass production of freshwater rotifers on liquid wastes. I. The influence of some environmental factors on population growth of Brachionus rubens Ehrenberg 1838 M. Schliiier and J. Groeneweg (Jiilich, Federal Republic of Germany) 17 Mass production of fresliwater rotifers on liquid wastes. II. Mass production of Brachionus rubens Elirenberg 1838 in the effluent of high-rate algal ponds used for the treatment of piggery.vaste J. Groeneweg and M. Schliiter (Julich, Federal Republic of Germany) 25 Carbotiydrate in rainbow trout diets. III. Growth and chemical composition of fish from different families fed four levels of carbohydrate in the diet o T. Ref.stie and E. Austreng {As, Norway) 35 Tetraploid rainbow trout produced by cytochalasin B T. Ref.'itie (As, Norway) 51 Factors affecting androgen sex reversal of Tiiapia aurea W.L. Shelton, D. Rodriguez-Guerrero and J. Lopez-Macias (Auburn, AL, U.S.A.)... 59 Growth, food intake and evacuation rates of grass carp, Ctenopbaryngodon ide'la fry S.S. De Silva (Matara, Sri Lanka) and D.E.M, Weerakoon (Colombo, Sri Lar ka).... 67 Comparative effects of diets consisting of one or two algal species upon assimilation efficiencies and growth of juvenile oysters, Crassostrea virginica (Gmelin) H.P. Romberger and C.E. Epifanio (Lewes, DE, U.S.A.) 77 Brief Technical Note The use of a biodeposition collector for estimation of assimilation efficiency in oysters C.C. Valenti and C.E. Epifanio (Lewes, DE, U.S.A.) 89 Short Communication Fecui dity and spawning frequency of Sarotherodon gaiiiaeus in a concrete pcnd J. Blay, Jr. (Achimota, Ghana) 95