The effect of prey type and density on the foraging efficiency of juvenile perch, (Perca fluviatilis)

The foraging efficiency of juvenile perch (Perca fluviatilis), feeding on two types of prey, was studied in laboratory experiments. Waterfleas (Daphnia magna) and phantom midge larvae (Chaoborus flavicans) were offered in a range of densities, either separately or combined. Perch fed more efficiently on each prey type separately than when both were mixed. Foraging efficiency decreased with an increase of mixed prey density with both prey types present in equal numbers, but also when the proportion of Chaoborus increased. This could be caused by the existence of different hunting techniques, each of which is fully efficient in the presence of one prey type only. In the presence of two prey types, the predator constantly has to switch from one hunting technique to another.     

The distribution and abundance of young (I +–II +) perch, Perca fluviatilis L., in a deep eutrophic lake, England

Seasonal changes in the vertical and horizontal distribution of young (I +–II +) perch in Rostherne Mere, a deep (max. depth 31.0 m) eutrophic lake are described using sonar. During the summer (June–August), perch were present within the thermocline (9–14° C) between 7 and 10 m. There was no significant difference between samples during this period, nor was there any evidence of shoaling. From September onwards perch moved into deeper waters. By late winter fish had become patchy in their distribution. Total numbers, during the summer, were estimated to be 988 ha ¹ with 95% confidence limits of ±115 (biomass 98.8 kg ha ⁻¹). Densities (no. m⁻³) fell by over 90% after the autumn overturn. The implications for predators are discussed. Acoustic sampling provides a useful, non-destructive method of sampling eutrophic lakes on a routine basis. Information obtained is of ecological, behavioural and physiological interest.     

Comparing fish catches taken with gill nets of different combinations of mesh sizes

Based on net selectivity curves and the pooled relative efficiency of combinations of mesh sizes, models for comparing gill-net catches taken with different combinations of mesh sizes are presented for perch, burbot and, in more detail, for salmonids. The models enable comparison of length frequencies and the numbers of fish within any length range caught with an acceptable net efficiency. A standard for comparing salmonids is proposed.     

河鲈养殖与野生群体遗传多样性比较分析

正河鲈(Perca fluviatilis),又名五道黑,五彩斑鱼,于比利牛斯半岛以外的全欧洲,以及黑海、里海和咸海等水系广泛分布,是我国乌伦古河水系及额尔齐斯河的主要土著鱼类。为鲈形目(Perciformes)、鲈亚目(Percoidei)、鲈科(Percidae)、鲈属(Perca)的一种名贵肉食性冷温带淡水鱼~[1]。     

An application of a bioenergetics model to Eurasian perch (Perca fluviatilis L.)

A bioenergetics model was developed for Eurasian perch ( Perca fluviatilis L.) by revising an existing model for yellow perch and walleye. Data were gathered from field studies and the literature. Besides adjusting the original parameters of the model, effects of season on consumption and metabolic rates were added. The predictive capability of the revised model was high both concerning the levels of growth and its seasonal development in the Baltic coastal waters to which the model was applied. Perch young-of-the-year attained almost maximum consumption and growth except in the highest temperatures experienced. In larger fish, the model estimated consumption to be about 50 per cent of the maximum possible rate.     

Laboratory evaluation of two bioenergetics models applied to yellow perch: identification of a major source of systematic error

Laboratory growth and food consumption data for two size classes of age 2 year yellow perch Perca flavescens , each fed on two distinct feeding schedules at 21° C, were used to evaluate the abilities of the Wisconsin (WI) and Karas–Thoresson (KT) bioenergetics models to predict fish growth and cumulative consumption. Neither model exhibited consistently better performance for predicting fish body masses across all four fish size and feeding regime combinations. Results indicated deficiencies in estimates of resting routine metabolism by both models. Both the WI and KT models exhibited errors for predicting growth rates, which were strongly correlated with food consumption rate. Consumption-dependent prediction errors may be common in bioenergetics models and are probably the result of deficiencies in parameter values or assumptions within the models for calculating energy costs of specific dynamic action, feeding activity metabolism or egestion and excretion. Inter-model differences in growth and consumption predictions were primarily the result of differences in egestion and excretion costs calculated by the two models. The results highlighted the potential importance of parameters describing egestion and excretion costs to the accuracy of bioenergetics model predictions, even though bioenergetics models are generally regarded as being insensitive to these parameters. The findings strongly emphasize the utility and necessity of performing laboratory evaluations of all bioenergetics models for assurance of model accuracy and for facilitation of model refinement.     

Variation in food intake within groups of juvenile perch

The coefficient of variation of individual food intake was large in small groups of young-of-the-year perch Perca fluviatilis (45–60 mm L _T) and smaller when fish that were given the same feeding rank were placed together. No aggressive interactions were detected during feeding.     

Genetic divergence and phylogeographic relationships among european perch (Perca fluviatilis) populations reflect glacial refugia and postglacial colonization

We used the widely distributed freshwater fish, perch (Perca fluviatilis), to investigate the postglacial colonization routes of freshwater fishes in Europe. Genetic variability within and among drainages was assessed using mitochondrial DNA (mtDNA) D-loop sequencing and RAPD markers from 55 populations all over Europe as well as one Siberian population. High level of structuring for both markers was observed among drainages and regions, while little differentiation was seen within drainages and regions. Phylogeographic relationships among European perch were determined from the distribution of 35 mtDNA haplotypes detected in the samples. In addition to a distinct southern European group, which includes a Greek and a southern Danubian population, three major groups of perch are observed: the western European drainages, the eastern European drainages including the Siberian population, and Norwegian populations from northern Norway, and western side of Oslofjord. Our data suggest that present perch populations in western and northern Europe were colonized from three main refugia, located in southeastern, northeastern and western Europe. In support of this, nested cladistic analysis of mtDNA clade and nested clade distances suggested historical range expansion as the main factor determining geographical distribution of haplotypes. The Baltic Sea has been colonized from all three refugia, and northeastern Europe harbours descendants from both eastern European refugia. In the upper part of the Danube lineages from the western European and the southern European refugia meet. The southern European refugium probably did not contribute to the recolonization of other western and northern European drainages after the last glaciation. However, phylogenetic analyses suggest that the southern European mtDNA lineage is the most ancient, and therefore likely to be the founder of all present perch lineages. The colonization routes used by perch probably also apply to other freshwater species with similar distribution patterns.     

Growth,Reproduction and Condition of Roach (Rutilus rutilus (L.)), Perch (Perca fluviatilis,L.) and Ruffe (Gymnocephalus cernuus (L.)) in Eutrophic Lake Aydat (France)

The growth, reproduction and condition of adults of the three dominant fish species (roach, Rutilus rutilus, (L.); perch, Perca fluviatilis, L. and ruffe, Gymnocephalus cernuus, (L.)) in the eutrophic Lake Aydat were studied over one year cycle. Compared to published data, the growth of R. rutilus and G. cernuus was about average, while that of P. fluviatilis was below average. Comparing to literature, the fecundity of R. rutilus and G. cernuus was low but their oocytes were large. In contrast, P. fluviatilis had a high fecundity but small oocytes. At the end of summer, an abrupt decrease in the condition was recorded only for perch, probably due to stress as a result of environmental conditions. The sex-ratio was in favour of females for the three studied species but, in contrast to G. cernuus, the sex-ratio of R. rutilus and P. fluviatilis increased significantly also with age. It is concluded that Lake Aydat is a more favourable environment for R. rutilus and G. cernuus than for P. fluviatilis.     

Evaluation of low impact pressure waves as a quantitative sampling method for small fish in shallow water

Low impact pressure waves (LIMP) generated by small (< 1 g) underwater ignition capsules have been used to qualitatively and semi-quantitatively, as catch per unit effort, sample young-of-the-year (YOY) and juvenile fish in shallow (0-3 m) waters. In order to evaluate this method on small fish, four categories, 0+ and 1+ year Eurasian perch, 1+ year roach and 0+ to 1+ year pike, were subjected to the LIMP at distances of 0.5-5 m from the detonation point. At a distance < 1 m all specimens were stunned and either floated to the surface or sank to the bottom, whereas almost all were unaffected at distances > 3 m. The efficiency radius of the LIMP varied between 1.5 and 3.0 m, and the effective area was 7-28 m² depending on habitat and species. The average effective area for the two extensively studied categories (0+ perch and 1+ roach) was 17.9 m². Both depth and vegetation affected the effective area. The smallest area was obtained at < 1 m depth with vegetation present, and the largest at 1-2 m depths with no vegetation present. Within each fish category, the method sampled fish independently of length suggesting that a size/year-class is sampled equally. The proportion of affected fish that sank was large and species-dependent. In addition to the netting of surfaced fish, collecting fish from the bottom is recommended for achieving an accurate quantitative estimate. The tested parameters of the LIMP, P_max and Impulse, declined as a function of distance following a negative exponential growth model with a baseline. The similar-shaped responses among the fish categories suggest that the method works at depths < 3 m also in heterogeneous environments, and that the method can be used to quantitatively estimate abundance of small fish with swim bladders. A model for quantitative abundance estimates based on the evaluation is presented.