22 resultados para Frequency-dependent parameters
Resumo:
The seasonally oscillating growth parameters and length-weight relationships for Scomber japonicus caught in the Gulf of Guayaquil, Ecuador, were determined based on length-frequency data from 1989 to 1996, using the FiSAT software package of Gayanilo et al. (1996). Estimates of growth parameters are in general agreement with previous studies on the same species. Results also imply that the growth of Scomber japonicus slows down during the cold season by approximately 50% with respect to the average growth. The mean value of the power b is significantly larger than 3, indicating that the model of allometric growth should be used for the length-weight relationship and calculation of the condition factor.
Resumo:
We consider estimation of mortality rates and growth parameters from length-frequency data of a fish stock and derive the underlying length distribution of the population and the catch when there is individual variability in the von Bertalanffy growth parameter L∞. The model is flexible enough to accommodate 1) any recruitment pattern as a function of both time and length, 2) length-specific selectivity, and 3) varying fishing effort over time. The maximum likelihood method gives consistent estimates, provided the underlying distribution for individual variation in growth is correctly specified. Simulation results indicate that our method is reasonably robust to violations in the assumptions. The method is applied to tiger prawn data (Penaeus semisulcatus) to obtain estimates of natural and fishing mortality.
Resumo:
At decadal period (10-20 years), dynamic linkage was evident between atmospheric low pressure systems over the North Pacific Ocean and circulation in a Pacific Northwest fjord (Puget Sound). As the Aleutian low pressure center shifts, storms arriving from the North Pacific Ocean deposit varying amounts of precipitation in the mountains draining into the estuarine system; in turn, the fluctuating addition of fresh water changes the density distribution near the fjord basin entrance sill, thereby constraining the fjord's vertical velocity structure. This linkage was examined using time series of 21 environmental parameters from 1899 to 1987. Covariation in the time series was evident because of the strong decadal cycles compared with long-term averages, interannual variability, and seasonal cycles.
Resumo:
An account and review of the simple methods for determining the operational parameters of fishing gear, underwater, such a tilt of otter boards (outwards or inwards, forwards or afterwards), vertical height of net, its horizontal spread, angle of divergence at bosom, spread between wing tips, angle of inclination of danlenos, butterfly, slope of legs and sweep-line has been given. The relationship of distance between the otter boards spread and the vertical height of net has been obtained as generally linear. The possibilities of regulating the vertical height of net (dependent variate) and spread of otter boards (independent variate) for increasing the fishing efficiency has been discussed. The angle of attack of oval shaped otter boards used during the operations still remain undetermined, however, it has been explained how the best angle of attack for increasing the efficiency of gear can be obtained by regulating the ratio of depth to warp for a given net. The inadequacy of the mere indices of catch per hour of trawling in comparing the relative efficiency of trawls in gear research studies has been indicated. The importance of estimating the operational parameters and its application to commercial fisheries depending upon the distribution pattern of fish and in gear research has been discussed. The efficiency of the jelly bottle method has been compared statistically with the observations made on the trawl gear underwater with instruments.
Resumo:
Data on age and growth of the following species were reviewed and von Bertalanffy's growth curves were fitted: Hilsa kelee, Decapterus russellii, D. macrosoma, Rastrelliger kanagurta, Pellona ditchela, Thryssa vitrirostris and Leiognathus equulus. For the five first species, microstructures in the otoliths were used for ageing. For most species growth curves based on size-frequency distributions are also presented. The reliability of the data presented is discussed.
Resumo:
A laboratory-feeding trail was conducted for 45 days with fry of common carp Cyprinus
carpio L. (0.45±0.03g) in aquaria in a static indoor fish rearing system. The fry were fed
on a pelleted diet containing 33% crude protein having fishmeal as major protein source.
The fish fry in five treatments A, B, C, D, and E, each with two replicates were fed on 5%
daily ration divided into different feeding frequencies of 2, 3, 4, 5 and 6 times a day
respectively in order to observe the growth performance. Each replicate contained 15 fry
having total initial weight of 6.87±0.31g. At the end of the feeding trial, significantly
different and higher (p<0.05) growth response was observed in treatment C having a
feeding frequencies of 4 times a day. Significantly the highest and the lowest percent
growth of 334.30 and 218.91% were observed in fish fed on the diet (Treatment C) with 4
times and (Treatment A) 2 times feeding frequencies per day, respectively. Food
conversion ratio (FCR) of 1.78 was significantly higher (p
Resumo:
Length-frequency data collected from fish landings on Lake Naivasha were used to estimate the growth parameters: total mortality (Z), growth performance index (Ø’), exploitation rate and recruitment pattern in Oreochromis leucostictus. The asymptotic length (L∞) was 38 cm and K 0.48 yr -1 Z was estimated as 3.5 yr -1, M was 0.19 yr -1, F was 2.6 yr -1 and E of 0.74. Recruitment occurs throughout the year, with a peak in January to March, while entry into the fishery occurs at a mean length of 15.9 cm. Existing restriction on the maximum number of gill nets allowed per fishing licence (10 per boat) and a minimum mesh size (10 cm) in the lake are not adhered to. Poaching using illegal mesh size nets as small as 5 cm and use of more than 10 nets per boat are common in the lake.