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Effects of thermal amplitude of diel fluctuating temperature on the growth, food consumption, food conversion efficiency and apparent digestibility coefficient of Chinese shrimp, Fenneropenaeus chinensis (Osbeck), with initial body weight of 0.36 ± 0.04 g were studied at average temperature 25, 28 and 31 °C from May to July, 2000. Among four diel different fluctuation amplitudes of ± 1, ± 2, ± 3 and ± 4°C, the growth rate of shrimp at 25 ± 2, 25 ± 3, 28 ± 2 and 31 ± 1 °C were significantly higher than those at corresponding constant temperatures of 25, 28 and 31 °C, respectively, while growth rate at 31 ± 4 °C was significantly lower than at 31 °C. There is a trend that the optimal thermal amplitude for shrimp growth decreased with the increase of average temperature in the present study. The growth rate of Chinese shrimp was a quadratic function of the thermal amplitude at the same average temperature. Such a growth model may be described byG=β0+β1(TA)+β2(TA)2where G represents the specific growth rate on a 33-day basis, TA is thermal amplitude in degree Celsius, β0 is intercept on G axis, and β1 and β2 are the regression coefficients. The optimal thermal amplitude for the growth of shrimp at sizes of this experiment at average temperature of 25, 28 and 31 °C was estimated to be ± 2.0, ± 2.2 and ± 1.4 °C, respectively. The changes of food conversion efficiency were similar to the growth rate, while the trends of food consumption of shrimp between fluctuating temperature and constant temperature were variable at different average temperatures. There was no significant difference in apparent digestibility coefficient between diel fluctuating temperatures and corresponding constant temperatures. Therefore, more food consumption, high food conversion efficiency and more energy partitioned into growth might account for the enhancement in the growth of shrimp at the diel fluctuating temperatures in the present study.  相似文献   

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The common practice among researchers who study fish growth is to a priori adopt the von Bertalanffy growth model (VBGM), which is the most used and ubiquitous equation in the fisheries literature. However, in many cases VBGM is not supported by the data and many species seem to follow different growth trajectories. The information theory approach frees the researcher from the limiting concept that a ‘true’ growth model exists. Multi‐model inference (MMI) based on information theory is proposed as a more robust alternative to study fish growth. The proposed methodology was applied to 133 sets of length‐at‐age data. Four candidate models were fitted to each data set: von Bertalanffy growth model (VBGM), Gompertz model, Logistic and the Power model; the three former assume asymptotic and the latter non‐asymptotic growth. In each case, the ‘best’ model was selected by minimizing the small‐sample, bias‐corrected form of the Akaike information criterion (AICc). To quantify the plausibility of each model, the ‘Akaike weight’wi of each model was calculated. Following a MMI approach, the model averaged asymptotic length for each case was estimated, by model averaging estimations of interpreting Akaike weights as a posterior probability distribution over the set of candidate models. The VBGM was not selected as the best model in 65.4% of the cases. Most often VBGM was either strongly supported by the data (with no other substantially supported model) or had very low or no support by the data. The estimation of asymptotic length was greatly model dependent; as estimated by VBGM was in every case greater than that estimated by the Gompertz model, which in turn was always greater than that estimated by the Logistic model. The percentage underestimation of the standard error of , when ignoring model selection uncertainty, was on average 18% with values as high as 91%. Ignoring model selection uncertainty may have serious implications, e.g. when comparing the growth parameters of different fish populations. Multi‐model inference by model averaging, based on Akaike weights, is recommended as a simple and easy to implement method to model fish growth, for making robust parameter estimations and dealing with model selection uncertainty.  相似文献   

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Understanding the processes that drive reproductive success in marine fish stocks is critical to effective fisheries management. These processes can be difficult to investigate, especially in age-structured populations, because they occur at transgenerational scales. Reproductive success is often attributed to a small portion of the adult population (<0.01%) and thought to be driven primarily by random external factors, consistent with the concept of sweepstake reproductive success (SRS). A competing concept, the reproductive resilience paradigm, posits that fishes have evolved complex spawner-recruit systems to achieve lifetime reproductive success and maintain population stability within highly variable environments. Here, we examine these two concepts. First, we analyse the popular sport fish red drum (Sciaenops ocellatus, Sciaenidae), drawing on genetic and reproductive data to estimate a plausible range for the ratio of effective population size ( N e ) to adult abundance ( N A ) and to infer variance in lifetime reproductive success ( V k * ). Then, we synthesize available data and infer V k * for two other fishes that have N e / N A ratios reportedly >0.10, the southern bluefin tuna (Thunnus maccoyii, Scombridae) and the silver seabream (Chrysophrys auratus, Sparidae). Although commonly regarded as an SRS species, red drum did not meet the SRS criterion. Overdispersed V k * values were inferred for all three species, with those for red drum and silver seabream being dependent upon population-closure assumptions. Results are presented within the conceptual framework of reproductive resilience, considering the roles of random extrinsic forces versus evolved traits to achieve lifetime reproductive success and population stability in high and variable mortality environments.  相似文献   

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The design of aquaculture systems requires an understanding of the drag forces on cultivated kelp. This study measured the drag on line segments of cultivated Saccharina latissima in a towing tank. The drag on segments of farm line with full kelp bundles and with stipes alone (fronds removed) was measured at tow speeds of 0.10 to 0.50 m/s. The drag on individual fronds cut from the line was also measured. Video images were collected to evaluate the plant reconfiguration. Both kelp blades and stipes contributed to the total drag force on the line bundle. Within the velocity range of our experiments, the kelp blades were essentially horizontal. However, the pronation of kelp stipes increased as flow velocity increased. The reconfiguration of kelp stipes was observed to decrease the vertical extent of the kelp bundle. Due to this reconfiguration, the measured force, F, increased with velocity, U, at a rate slower than quadratic, and was consistent with scaling laws derived for reconfiguration. Specifically, FUα with α=1.35±0.17.  相似文献   

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Eggs stripped from Coregonus albula were incubated at different constant temperatures. The duration of embryogenesis varied from 183 days at 1.1°C to 45 days at 9.9°C. We describe the course of embryogenesis using 16 easily recognizable developmental stages (DS j). Development rate (DR j) for any given stage (DS j) is expressed as the reciprocal of time (in days) from fertilization to attainment of a given developmental stage. The generalized equation relating rate of development to stages DS j with respect to temperature (x) is
DRj= abx cx2 dx3 fx4
The values of DR to the “eyed egg” stage and to 50% hatch, expressed as percentage per day of the total development period, were computed and tabulated for temperatures ranging from 0.1 to 9.9°C. To verify the derived regression model we observed the course of embryogenesis of C. albula eggs incubated in a commercial hatchery at fluctuating temperatures. The observed times of attainment of the successive developmental stages were compared to the predicted times based on mean daily water temperatures. The time observed agreed well with times predicted by the model; the only exception was the time of hatching, which was systematically overestimated (5 to 7 days) by the model. This was possibly due to the influence of dissolved oxygen on the time course of hatching processes, which was not considered in our regression model.  相似文献   

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