6 resultados para COURTSHIP

em Aquatic Commons


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Many species of reef f ish agg regate seasonally in large numbers to spawn at predictable times and sites (Johannes, 1978; Sadovy, 1996; Domeier and Colin, 1997). Although spawning behavior has been observed for many reef fish in the wild (Wicklund, 1969; Smith, 1972; Johannes, 1978; Sadovy et al., 1994; Aguilar Perera and Aguilar Davila, 1996), few records exist of observations on the courtship or natural spawning for the commercially important family Carangidae (jacks) (von Westernhagen, 1974; Johannes, 1981; Sala et al., 2003). In this study, we present the first observations on the natural spawning behavior of the economically-valuable permit (Trachinotus falcatus)(Linnaeus, 1758) from the full to new moon period at reef promontories in Belize, with notes on the spawning of the yellow jack (Carangoides bartholomaei) (Cuvier, 1833), and the courtship of five other carangid species.

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An illustrated description is given of the courtship and mating behaviour of P. monodon . Courtship and mating follow three distinct phases: (1) parallel swimming of male and female from the bottom to a height of 20-40 cm over distances of 50 to 80 cm; (2) male turns ventral side up to female; and (3) male turns perpendicular to female, arches body around the female and lifts head and tail. Mating is believed to take place generally at night, following moulting of the female. On the basis of thelycum structure and mating pattern, Penaeus may be divided into two groups: (1) those with a close thelycum in which mating follows moulting, such as P. merguiensis and P. monodon ; and (2) those with open thelycum where mating takes place immediately preceding spawning, as in P. stylirostris and P. vannamei .

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Research on the basic reproduction processes of Gammarus is summarized and reviewed, reproductive strategies in males and females being left to two later papers. The author describes the reproductive systems, the development of eggs (oocytes) in the ovaries, courtship and precopulatory amplexus, mating and the production of sperms, egg laying, mortality and diapause.

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In this study we describe the courtship and spawning behaviors of captive yellowfin tuna (Thunnus albacares), their spawning periodicity, the influence of physical and biological factors on spawning and hatching, and egg and early-larval development of this species at the Achotines Laboratory, Republic of Panama, during October 1996 through March 2000. Spawning occurred almost daily over extended periods and at water temperatures from 23.3° to 29.7°C. Water temperature appeared to be the main exogenous factor controlling the occurrence and timing of spawning. Courtship and spawning behaviors were ritualized and consistent among three groups of broodstock over 3.5 years. For any date, the time of day of spawning (range: 1330 to 2130 h) was predictable from mean daily water temperature, and 95% of hatching occurred the next day between 1500 and 1900 h. We estimated that females at first spawning averaged 1.6−2.0 years of age. Over short time periods (<1 month), spawning females increased their egg production from 30% to 234% in response to shortterm increases in daily food ration of 9% to 33%. Egg diameter, notochord length (NL) at hatching, NL at first feeding, and dry weights of these stages were estimated. Water temperature was significantly, inversely related to egg size, egg-stage duration, larval size at hatching, and yolksac larval duration.

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Spawning behaviour of hormone induced estuarine catfish, Mystus gulio was observed in captive condition. Spawning activities that include pairing, chasing and resting, nudging, and twisting, started about 5 hours post injection and ended with release of eggs within 1-2 hours of courtship. Three different dosages of "ovaprim" (1 ml/kg, 1.5 ml/kg, and 2 ml/kg in a single dose) were used in induced breeding of M gulio. The latency period was less (6-7 hours) with the dose of 1.5 and 2 ml/kg, while it was more (7-8 hours) with that of 1 ml/kg. However, all females spawned successfully with each of three different dosages, without any significant differences in the rate of fertilization and hatching. Eggs under all hormone dosages hatched between 18-20 hours after spawning. The hatching rate with 1, 1.5, and 2 ml/kg varied from 71.3-72.7%, corresponding to the fertilization rate of 80.7-84.7%.

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Induced breeding of Clarias gariepinus was conducted monthly in hapa pens, set up in Otamiri river for nineteen months (June 1993 - December 1994). Results of natural fertilization were unsatisfactory as few eggs were fertilized. Mean relative fecundity, percentage fertilization, percentage hatching and percentage fry survival were: 15.86 ± 1.95 x 10', 18.92 ± 5.28%, 13.50 ± 3.8% and 6.42 ± 0.72%. Results from artificial fertilization were as follows: Mean relative fecundity, 13.80 ± 2.85 x 10', percentage fertilization, 81.91 ± 2.28%, percentage hatching, 86.10 ± 2.46% and percentage fry survival, 21.40 ± 1.89% respectively. The success of artificial fertilization depended largely on the latency period of 9-11 hours and this suggests that induced breeding in pens is feasible. The poor results from natural fertilization were attributed to lack of adequate substrate for the male fish to display courtship and subsequent fertilization of eggs.