97 resultados para Ordelaffi, Francesco, d. 1374.


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Euphausiids vertical distribution on the Côte d'Ivoire continental shelf during different seasons, average zonal distrubution, mean distance to the shore, and seasonal variations in abundance computed for five years, suggest that the appearance, and the shifting of euphausiids across and along the shelf are related with the variations of the distance from the shore of the ivorian under-current. The author reports that Nyctiphanes capensis has not been found in the region.

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From Aug 1975 to Jan 1976 a fishing survey for deep-sea red crab Geryon quinquedens was executed along the Ivorian coast between 3{degree} and 7{degree}30'W. Three regions could be distinguished: a central one with poor catches (1.6 kg/trap/20h); an east region with the best catches (5 kg/trap/20h); and a west region, also with good catches (4.5 kg/trap/20h). For the whole survey, catches only took place between 300 and 700m, the best at 400 m. A distinct sexual segregation was observed according to bathymetry with the percentage of males increasing with depth. Nearly the same abundance was observed in Côte d'Ivoire, in Congo and North Angola, while in South Angola catches are somewhat higher.

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Descriptions of spawning and larval development of Ethmalosa, up to the vitelline vesicle resorption stage, are made from plankton samplings in the Ebrié coastal lagoon and from artificially fertilized eggs. Spawning takes place from November to June in waters with salinities of 18 to 26 parts per thousand, and temperatures of 22.8 to 30.2 degrees, for 13-14 cm long fishes.

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Seasonal variations of abundance and vertical distribution over the shelf are investigated for Ostracoda, Cladocera and Cirripede larvae. The main characteristics of the environment are the periodical enrichments mainly caused by upwellings, secondly by the river floods. Ostracoda abundance variations approximately follow phytoplankton outburst. Breeding occurs all over the year. Their vertical distribution is correlated with a discontinuity layer. Diurnal migration, when it occurs in warm season consists in an upward movement during the night towards surface layers. The Ostracoda inhabit bottom layers during the day and migrate at night in intermediate and surface layers. For the main two species of Cladocera, Penilia avirostris and Evadne tergestina, abundance periods follow upwellings, especially during the main cool season. However, Cladocera can grow in low salinity but rich waters. On average Penilia inhabits more superficial waters in cold than in warm seasons. Cirripede nauplii and cypris are more abundant off rocky coasts. Their maxima are in the upwelling periods.

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Cumacea were only observed in night plankton of the Côte d'Ivoire continental shelf. However they are not always observed and their occurrence seems to depend on the marine seasons. In September, December and April, the catches were very poor indeed, whereas May and June showed interesting results. Most of the species are rarely seen in the upper layer. Several activity rhythms could be shown for the most common species present in the hauls.

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Methods for the estimation of zooplankton biomasses, used in the Oceanographic Research Center of Abidjan are presented. They deal with settled and displacement volumes, dry weight and ash-free dry weight, elementary carbon, nitrogen and phosphorus composition. The dry weight method is detailed: elimination of salt by a fresh water stream, preservation of dry samples at -20 degrees Celsius, rehydration during weighing. A few comments on the 'CHN' analysed values are made: at 1,100 degrees Celsius, most of the carbon is organic, only 10% of the mineral fraction being analysed.

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Spawning of bonga (Ethmalosa fimbriata Bowdich) takes place in polyhalin waters (Sppt. > 5ppt.). Migrations of young fish were studied by the mean of length data observed in different points of the lagoon from the artisanal fishery. Bonga remain 4 months in the hatchery (6 cm), before they expand in the whole lagoon until the age of 9/10 months. After this expansion phase, the fishes come back to the spawning fields (spawning length: 14/15 cm). Postspawning fishes leave the lagoon. Between birth and spawning, bonga are not affected by salinity changes, but reproduction occurs only in waters where salinity is higher than 5ppt.

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This paper describes the fishery of Côte d'Ivoire and its evolution to the present day. The location of fishing off Côte d'Ivoire is specified for each area and each type of trawler. A comparison of productivity between the different areas shows disparities that allow to make clearer the repartition of effort of all types of trawlers in each area. The Côte d'Ivoire continental shelf is populated with demersal stocks of homogeneous densities.

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Graphs of variations of zooplankton biomasses expressed as ash-free dry weight (i.e. organic matter) are presented for the 1969-1979 period. The graph of the average year shows: an enrichment season from mid-July till mid-November in which the biomass is 2.3 times higher than the rest of the year and characterized by a slight decrease of the biomass in late August or early September. The warm season is divided into a period of moderate biomass from November till February, a period of moderate biomass from November till February and a period of steady decline of the biomass till the start of the upwelling at the end of June.

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Data are reported on: (1) date and place of ringing the juveniles and adults of the sea bird of the genus Sterna in Côte d'Ivoire, and (2) date and place of recapture during the winter periods of 1973-74 and 1974-75.

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Petersen disc tag marking experiments confirm the influence of animal size and marking time on the recapture rate. Westward migrations occur, probably following the Ivorian undercurrent. Catchability coefficients have been evaluated for the Grand-Bassam fishing ground and tentatively extrapolated to the other fishing areas. The extrapolated non weighted coefficient for the entire fishing areas is q=0.00069/fishing day for an area of 390 miles. The instantaneous coefficient of residual mortality X taken as a first and possibly slightly overestimated value of M the natural mortality, has been estimated at 0.155/month, strongly corroborating Berry's results (1967). This value is however much smaller than that given by earlier authors. It is suggested that q could have a higher value during the very first weeks of exploitation at sea, when the juveniles are concentrated near the lagoon outlets.

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The occurrence of seasonal variations in growth is confirmed. The mean annual growth curve obtained is not different from that obtained by modal progression analysis. The comparison with results obtained by other authors in Florida did not permit to point out any sensible difference and the author concludes that the phenomena are quite similar but that it would be better, for yield computations, to use the observed age-length keys instead of the computed parameters.

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Von Bertalanffy's growth curve parameters K, L∞ and t'o have been estimated for female Penaeus duorarum by modal progression analysis, using the "successive maximums method" of Gheno and Le Guen (1968) for the polymodal size frequency curves analysis and the Tomlinson and Abrahamson's least squares method for parameters computations. For the male the authors used an original method to get an age/length key. The parameters were calculated by Gulland's graphical method (1969).

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The analysis of the geographic and bathymetric distribution of Penaeus duorarum and, particularly P. d. notialis off Côte d'Ivoire and in its whole distribution area leads to the definition of the adult ecological requirements (temperature, salinity, grain size and sediment composition, organic matter) and the importance of the thermocline in the bathmetric distribution. The population structure study shows: (1) variations of size with depth, (2) variations of sex ratio, with size, depth and seasons.

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A computer program has been written in order to generate a population of fishes following a Von Bertalanffy growth curve with a random Gaussian variability for birth dates and growth parameters K and L ∞. Standard deviations for these 3 parameters are chosen separately for each run. Fishing and natural mortalities are applied to this population. Using as an input parameters usually taken for yellowfin in the eastern Atlantic, the simulation suggests a standard deviation between 1 and 2 months for the birth dates in this population. It also indicates that increasing levels of fishing mortalities must produce a better agreement between age and length for the larger fish.