Effects of temperature and photoperiod on ovarian recrudescence in the cyprinid fish Mirogrex terrae‐sanctae

Mirogrex terrae-sanctae is a commercial, sardine-like cyprinid fish in the Sea of Galilee. The fish spawns from December to the end of March. Females collected at the quiescent phase of the cycle (June) were exposed to four combinations of photoperiod and temperature for 3 months. The highest GSI (2.44 ± 0.22) was found in females exposed to simulated winter conditions (16°C, 9L) while the lowest GSI (0.65 ± 0.04) was found in fish exposed to simulated summer conditions (27°C, 14L). The GSI of fish maintained at the unnatural combination of 16°C, 14L (1.30 ± 0.09) did not differ from that of fish maintained at the other unnatural combination of 27°C, 9L (1.07 ± 0.11). However, histological examinations revealed that vitellogenic oocytes were present only in fish maintained at low temperature regimes, which implies that the growth of the ovarian mass in the 27°C, 9L group was due mainly to oogonial proliferation and that vitellogenesis was inhibited in Mirogrex at a high temperature. Both protein and calcium concentrations increased in the serum of fish following injections of oestradiol-17β. The increase of calcium was evident only in the non-filtrable (bound) fraction, suggesting that the total serum calcium above 13 mg% could be used as an indirect parameter for circulating vitelloprotein. Fish collected at the quiescent phase were injected with oestradiol (50 μg/fish c. 15 g body weight) and subsequently transferred to tanks maintained at either 12°, 20° or 27°C. The total serum calcium increased to 23.0 ± 1.75 mg% in the fish maintained for 8 days at 20°C. This was significantly higher than the concentration of calcium in the serum of fish maintained at either 12°C (7.8 ± 0.52) or 27°C(l1.8 ± 0.77). This implies that the temperature may affect ovarian recrudescence by modulating the response of the liver to oestrogen, allowing the oestrogen-induced vitellogenesis to be relatively high in the cool environment during winter.

[1]  F. Menn Some aspects of vitellogenesis in a teleostean fish: Gobius niger L , 1979 .

[2]  M. Hodgins,et al.  Distribution of androgen metabolizing enzymes in isolated tissues of human forehead and axillary skin. , 1978, The Journal of endocrinology.

[3]  R. Billard,et al.  Ultrastructural studies on experimentally induced vitellogenesis in juvenile rainbow trout (Salmo gairdneri R.) , 1978 .

[4]  C. Gillet,et al.  Seasonal effects of exposure to temperature and photoperiod regimes on gonad growth and plasma gonadotropin in goldfish (Carassius auratus) , 1978 .

[5]  N. Bromage,et al.  The effects of alterations in photoperiod on ovarian development and spawning time in the rainbow trout (Salmo gairdneri) , 1978 .

[6]  Z. Yaron,et al.  Estrogens and estrogenic effects in Tilapia aurea (Cichlidae, Teleostei) , 1978 .

[7]  H. Salzer,et al.  Occurrence and biological activity of estradiol-17 beta in the intact and ovariectomized Tilapia aurea (Cichlidae, Teleostei). , 1977, General and comparative endocrinology.

[8]  V. L. Vlaming,et al.  Effects of pinealectomy on pituitary gonadotrophs, pituitary gonadotropin potency and hypothalamic gonadotropin releasing activity in Notemigonus crysoleucas , 1977 .

[9]  D. Idler,et al.  Hormonal control of vitellogenesis in hypophysectomized winter flounder (Pseudopleuronectes americanus walbaum). , 1976, General and comparative endocrinology.

[10]  V. L. Vlaming,et al.  Effects of photoperiod-temperature regimes on pituitary gonadotrophs, pituitary gonadotropin potency and hypothalamic gonadotropin releasing acitivity in the teleost notemigonus crysoleucas , 1976 .

[11]  I. Petersen,et al.  Natural occurrence, and experimental induction by estradiol-17-beta, of a lipophosphoprotein (vitellogenin) in flounder (Platichtys flesus, L.). , 1976, Comparative biochemistry and physiology. B, Comparative biochemistry.

[12]  B. Emmersen,et al.  Protein, RNA, and DNA metabolism in relation to ovarian vitellogenic growth in the flounder Platichthys flesus (L.). , 1976, Comparative biochemistry and physiology. B, Comparative biochemistry.

[13]  S. Gupta The development of carp gonads in warm water aquaria , 1975 .

[14]  V. L. Vlaming Effects of photoperiod and temperature on gonadal activity in the cyprinid teleost, Notemigonus crysoleucas. , 1975, The Biological bulletin.

[15]  V. D. Vlaming The role of the endocrine system in temperature-controlled reproductive cycling in the estuarine gobiid fish, Gillichthys mirabilis. , 1972 .

[16]  V. D. Vlaming Environmental control of teleost reproductive cycles: a brief review , 1972 .

[17]  Z. Yaron Observations on the granulosa cells of Acanthobrama terrae-sanctae and Tilapia nilotica (Teleostei). , 1971, General and comparative endocrinology.

[18]  N. Fraser,et al.  Incorporation of l-[C]leucine into egg proteins by liver slices from cod. , 1971, The Biochemical journal.

[19]  D. Pritchard,et al.  Egg proteins in cod serum. Natural occurrence and induction by injections of oestradiol 3-benzoate. , 1971, The Biochemical journal.

[20]  Z. Yaron Correlation between spawning, water temperature and thyroid activity in Acanthobrama terrae-sanctae (Cyprinidae) of Lake Tiberias. , 1969, General and comparative endocrinology.

[21]  S. V. Goswami,et al.  Effects of estrogen, progesterone, and testosterone on the pituitary and ovary of catfish, Heteropneustes fossilis (Bloch). , 1968, The Journal of experimental zoology.

[22]  W. E. Vanstone,et al.  Effect of Estradiol Monobenzoate on some Serum Constituents of Maturing Sockeye Salmon (Oncorhynchus nerka) , 1961 .

[23]  M. Urist,et al.  The Partition of Calcium and Protein in the Blood of Oviparous Vertebrates during Estrus , 1961, The Journal of general physiology.

[24]  Robert Whiting Harrincton Sexual photoperiodicity of the cyprinid fish, Notropis bifrenatus (Cope), in relation to the phases of its annual reproductive cycle. , 1957 .

[25]  O. H. Lowry,et al.  Protein measurement with the Folin phenol reagent. , 1951, The Journal of biological chemistry.