Effective population size and temporal genetic change in stream resident brown trout (Salmo trutta, L.)

Temporal genetic data may be used forestimating effective population size (N _e) and for addressing the `temporal stability' of population structure, two issues of central importance for conservation and management. In this paper we assess the amount of spatio-temporal genetic variation at 17 di-allelic allozyme loci and estimate current N _e in two populations of stream resident brown trout (Salmo trutta) using data collected over 20 years. The amount ofpopulation divergence was found to bereasonably stable over the studied time period.There was significant temporal heterogeneitywithin both populations, however, and N _e was estimated as 19 and 48 for the twopopulations. Empirical estimates of theprobability of detecting statisticallysignificant allele frequency differencesbetween samples from the same populationseparated by different numbers of years wereobtained. This probability was found to befairly small when comparing samples collectedonly a few years apart, even for theseparticular populations that exhibit quiterestricted effective sizes. We discuss someimplications of the present results for browntrout population genetics and conservation, andfor the analysis of temporal genetic change inpopulations with overlapping generations ingeneral.     

Weight of food and time required to satiate brown trout, Salmo trutta L.

Brown trout of different weights (range 8-358 g) were fed to satiation at fifteen different water temperatures (range 3.8–21.6°C. Both the weight of the trout (Wg) and the water temperature (T°C) affected the maximum weight of food (Q mg) consumed in a meal, and the relationship between the three variables was well described by a multiple regression equation which can be used to estimate the value of Q (with 95% confidence limits) for trout of different weights at different temperatures between 3.8°C and 21.6°C. The satiation time (with 95% confidence limits) can also be estimated from a multiple regression equation for trout of different weights at temperatures between 6.8°C and 18.1°C. Estimates from the multiple regression equations were applicable to a wide range of food organisms with the exception of larvae ofTenebrio molitor (mealworms). Appetite (measured by voluntary food intake) varied with temperature and was greatest between 13.3°C and 18.4°C. From comparisons with the results of other workers, it was concluded that the maximum amount of food consumed in a meal may provide sufficient calories for both the daily metabolic requirements and the daily maintenance requirements of a trout at temperatures between 3.8°C and 18.4°C, but not at temperatures above 18.4°C.     

Rates of gastric evacuation in brown trout, Salmo trutta L.

Brown trout of similar length and weight were fed a standard meal which contained a known number of food organisms of the same size-group and taxon (seven taxa were used). The weight of digestible organic matter in a trout stomach decreased exponentially with time. i.e. at a constant relative rate. At a particular water temperature, the food organisms were either evacuated from the stomach at similar rates (Group 1: Gammarus pulex, Baetis rhodani, Chironomidae, Oligochaetes) or at progressively slower rates (Group 2: Protonemura meyeri, Hydropsyche spp., Tenebrio molitor). Rates of gastric evacuation were not significantly different for food organisms of different size groups of the same taxon, or for different sized meals, or for different sizes of trout (range 20–30 cm), or for mixed and multiple meals (three meals over 16 h). Times are given for the gastric evacuation of 50%, 75%, 90% and 99% of the digestible organic matter in a meal. Starvation periods of 1, 2, 3,4 and 5 days prior to feeding did not affect evacuation rates. The rates were slightly, but not significantly, slower for starvation periods of 6 and 7 days, and were often significantly slower for starvation periods of 10, 15 and 20 days. Evacuation rates increased exponentially with increasing water temperature. It was possible to estimate both the rate and time for the gastric evacuation of different meals at water temperatures between 3–8°C and 19·1°C.     

Validation of scale-reading estimates of age and growth in a brown trout Salmo trutta population

In this study, we validated a scale-reading method estimating age and growth in brown trout Salmo trutta in wild, landlocked, stream-dwelling populations from mountain headwaters in the Elbe catchment area of the Czech Republic. The values estimated from scale reading were compared with measured values, collected using a mark-recapture program over eight consecutive years. The age-corrected absolute percentage error was 10.71%, primarily because the ages of the oldest individuals according to scale reading were underestimated, and the ages of juvenile individuals were slightly overestimated. The back-calculated length was slightly underestimated (the mean error was ?4.60 mm), but it was not significantly different from the real measured length. This study suggests that in cold mountain headwaters, scale reading is a sufficiently accurate method for age and growth estimation in juvenile brown trout; however, the results for adult individuals must be taken with caution.     

Reproductive investment of female brown trout, Salmo trutta L., in a stream and reservoir system in northern England

Within the basin of Cow Green reservoir, upper Teesdale, the brown trout, Salmo trutta L., spend their first two seasons in running water. After this some females remain resident and others migrate to Cow Green reservoir. A cohort of 1000 females at age 2 that remains resident in tributary streams will, during the lifetime of the cohort, lay, on average, 3·0 times as many eggs as a cohort which resides in the reservoir. This conclusion is apparently not consistent with the observation that most females take up reservoir residence.
Reservoir females have a higher growth rate (Walford constant k=0·61, c.f. 0·86 for stream residents) and shorter life expectancy ( M year⁻¹= 1·19, c.f. 0·56) than the stream residents. However, they are of larger average size than the stream residents, lay larger eggs (mean 0·074 g, c.f. 0·066 g) and bury them more deeply (mean depth 11·0 cm, c.f. 8·5 cm).     

The downstream drifting of eggs of brown trout, Salmo trutta L.

The occurrence of eggs in the drift samples was not related to fluctuations in flow rates, but was probably related to the presence of eggs in the gravel. Both the number ( Y eggs 3h⁻¹) and density ( Y eggs 100⁻¹ m⁻³) of eggs in the drift samples increased with increasing water velocity ( V m sec⁻¹), and the relationship between the two variables was well described by the regression equation Y=a V^b where a and b are constants. Comparisons were made between two streams and different, years.     

Thermoregulatory behavior of brown trout,Salmo trutta

Brown trout, Salmo trutta, were allowed to thermoregulate individually in an electronic shuttlebox. Pooled data for 6 fish showed a diel pattern of preferred temperature, with a diurnal minimum of 10.3°C, an early nocturnal maximum of 13.7°C, a less pronounced mid-scotophase minimum of 11.7°C, and a secondary dawn maximum of 12.8°C, in a somewhat crepuscular pattern. The 24-hour mean preferendum was 12.2°C.     

Daily energy intake and growth of piscivorous brown trout,Salmo trutta

• 1 The chief objectives were to determine the daily energy intake and growth of piscivorous brown trout (Salmo trutta), and to compare the observed values with those expected from models developed previously for brown trout feeding on freshwater invertebrates. Energy budgets for individual fish were obtained from experiments with 40 trout (initial live weight 250–318 g) bred from wild parents, and kept at five constant temperatures (5, 10, 13, 15, 18 °C) and 100% oxygen saturation. Each trout was fed to satiation on freshly killed sticklebacks (Gasterosteus aculeatus) over a period of 42 days.
• 2 Energy intake (C_IN cal day^‐1) and growth (C_G cal day^‐1) were measured directly and energy losses (C_Q cal day^‐1) were estimated by difference (C_Q = C_IN ‐ C_G). All three variables increased with temperature. A model previously used to predict the daily energy intake (C_IN(INV)) of trout feeding to satiation on invertebrates was adapted, by changing only one parameter, to provide an excellent model (R² = 0.998) for predicting the mean daily energy intake (C_IN(ST)) for the piscivorous trout. Values of C_IN(ST) were 58% (range 48–67%) higher than those for C_IN(INV). A simple model was also developed to estimate mean daily energy losses for piscivorous trout (R² = 0.999). Both models were combined to provide excellent estimates of the daily energy gain (growth) of the piscivorous trout, and this was about three times that for trout feeding on invertebrates. The optimum temperature for maximum growth in energy terms increased from 13.9 °C for trout feeding on invertebrates to 17.0 °C (range 16.6–17.4 °C) for piscivorous trout.
• 3 The models are basically an extension of those developed for trout feeding on invertebrates. They show clearly how energy intake, growth, and the optimum temperature for growth increase markedly when trout change their diet from invertebrates to fish. The implications of this are discussed and it is shown that, in theory, these increases should continue if a more energy‐rich diet was utilised by the trout.

     

Home range of juvenile Atlantic salmon, Salmo salar, and brown trout, Salmo trutta, in a Norwegian stream

SUMMARY. 1. The sizes of home ranges of juvenile Atlantic salmon (age 1 +) and brown trout (age 2+ to 9+) in a Norwegian coastal stream were estimated by local movements of batch-marked fish from 12.5 and 25 m long sections. Only recoveries made in the release section and in up-and downstream neighbouring sections were considered.
2. There was no significant difference in the average percentage of recaptures of salmon and trout between 12.5 and 25 m sections; a stream area of about 40–50 m² defines the size of home range for stocks of both species.
3. The fraction of brown trout recaptured in release sections increased with increasing fish densities, indicating a smaller home range under these conditions.     

Population genetic structure of brown trout (Salmo trutta L.) within a northern boreal forest stream

Brown trout (Salmo trutta L.) population genetic structure and its temporal stability were studied within a small forest stream in central Sweden using five microsatellite loci. Both resident and migrating brown trout are present in the watershed. Tissue samples were collected from seven sections of the stream during two consecutive years. No differences were found in multilocus FST estimates between years within sections except in one case. Moreover, differences between age cohorts within sample sections were rare. The low interannual variation and the low heterogeny between cohorts is interpreted as indications of temporal stability. Pairwise multilocus FST estimates increased with increasing geographic distance, indicating isolation by distance. It is argued that the brown trout of the F?rs?n stream represent a population complex. The structure is probably maintained by precise natal homing and a limited, but important, amount of gene flow between closely situated sections within the stream supporting a stepping-stone model of gene flow.     

D(+)-Glucose permeability in brown trout Salmo trutta L. erythrocytes

D(+)-Glucose penetration in trout erythrocytes was studied with osmotic and tracer methods.
Results give no evidence for a carrier mediated diffusion system like that concerned with glucose permeability as in human red cells. The data show that glucose fails to stimulate erythrocyte respiration.     

Abundance and distribution of a brown trout (Salmo trutta, L.) population in a remote high mountain lake

Brown trout (Salmo trutta) population of a remote high mountain lake (Lake Redó, Pyrenees, 2240 m above sea level) were studied during autumn using hydroacoustic techniques. This acoustic technique was for the first time used on fish at such high altitude in Spain. Sampling using multimesh nets fish catches and echosounding recording were carried out in September 1998. Mean density of fish was estimated to be 1.82 fish per 1000 m³ (597 fish ha^–1). The results exhibited mainly a littoral habitat, with the brown trout being preferentially in the 10–25 m deep layer, where the water was warmer and the richness and diversity of macroinvertebrates higher. The sampling by hydroacoustic technique found a length frequency range of fish higher than the multimesh gill nets but both of them estimated similar fish proportion for the common length range. The more frequent target strength (TS) for the population was –38 dB (TS range –37 to –39 dB). Good correlation was found between TS frequency distribution obtained by echosounding and that predicted by means of a model based on the log of the fish total length from multimesh gill nets captures.     

Compensatory response 'defends' energy levels but not growth trajectories in brown trout, Salmo trutta L

Compensatory growth is an organism's reaction to buffer deviations from targeted trajectories. We explored the compensatory patterns of juvenile brown trout under field and laboratory conditions. Divergence of size and condition trajectories was induced by manipulating food levels in the laboratory and then releasing the trout into a river. In the stream, the length trajectories of food-restricted and control fish were parallel, but food-restricted fish exhibited partial compensation for mass and rapid recovery of condition. A laboratory experiment on similar sized fish did not provide evidence for compensatory growth in length or mass. In contrast, data matched the compensatory patterns shown in the stream: length trajectories were parallel and the convergence of mass trajectories ceased as soon as food-restricted fish recovered condition to the level of controls. These results show that (i) brown trout did not compensate for depression in structural growth and (ii) mass recovery was targeted to reinstate condition or energy reserves, but not size at a given age. This does not support the common view that compensatory growth can be a general response to growth depression. Rather, compensation in other salmonids could be related to size thresholds associated with developmental switches at the onset of sexual maturation and migration.     

Phosphoglucose isomerase isozymes and allozymes of the brown trout, Salmo trutta L

1. In brown trout the Pgi-1 and Pgi-2 loci are predominantly expressed in white skeletal muscle; Pgi-3 being mainly expressed in most other tissues. 2. Total PGI activity determinations revealed that the allele formerly designated Pgi-2(65) is a null allele, Pgi-2(n). 3. Enzyme kinetic studies on the partially purified PGI homodimeric isozymes revealed that from 5 to 25 degrees C both PGI-1 and PGI-2 had significantly higher mean Km(F6P) values compared to PGI-3. 4. Distinct metabolic roles for the "muscle" (PGI-1, PGI-2) and "liver" (PGI-3) isozymes are proposed. 5. Significant Km (F6P) differences were found among the PGI-2 allozymes and among the PGI-3 allozymes.     

Endocrine responses of brown trout, Salmo trutta L., to acid, aluminium and lime dosing in a Welsh hill stream

Brown trout caged in an acidic, softwater, Welsh hill stream running through close-canopy conifer forest and in an adjacent, circumneutral, moorland stream were studied after a natural rainfall event and after experimental acid and aluminium dosing of the forest stream. Endocrine (cortisol and thyroxine) and metabolic (glucose) stress responses occurred in fish held in the forest stream. Liming downstream of the acid zones mitigated these responses.     

Interpopulation variation in reproductive traits of anadromous female brown trout, Salmo trutta L.

We studied reproductive traits in nine anadromous brown trout, Salmo trutta L., populations in seven Norwegian rivers. Within populations we found a positive significant correlation between fish length and fecundity in all populations, and between fish length and egg diameter in five populations. There were significant differences in these relationships between populations from different rivers, and between populations from different locations within rivers. When adjusted for variation in fish length, mean fecundity and mean egg diameter showed a negative significant correlation among populations. The ratio of gonadal weight to somatic weight (gonadosomatic index) varied significantly among populations but was not associated with variation in fish length. Comparatively few large eggs were found in brown trout populations co-existing with several other fish species.     

Acidophilic granular cells in the epidermis of the brown trout,Salmo trutta L.

Summary Acidophilic cells occur in the epidermis of several species of salmonid fish, although their abundance fluctuates considerably between individuals within the same population and at different times during the life cycle. The histology, histochemistry and ultrastructure of an acidophilic, granular celltype in the epidermis of the brown trout, Salmo trutta L., is described. At the light microscope level this cell type is easily distinguished from the large, mucus-secreting, epidermal goblet cells by its acidophilic, proteinaceous secretion. At the ultrastructural level this secretion consists of membrane-bound granules formed by the very active Golgi region. It is argued that the acidophilic, granular cell is not a transformed blood cell but constitutes a normal epidermal component of the brown trout. Possible roles of this cell in the function(s) of the epidermis are discussed.     

Otolith shape discriminates between juvenile Atlantic salmon, Salmo salar L., and brown trout, Salmo trutta L.

Otoliths of Atlantic salmon, Salmo salar L., are more slender than the otoliths of brown trout, Salmo trutta L. Discriminant analysis on otolith measurements of juvenile Atlantic salmon and brown trout from four river systems revealed a discriminant function which distinguished more than 94% of the cases. This function was tested by using data from a fifth river with cohabiting Atlantic salmon and brown trout: all Atlantic salmon and 91 % of the brown trout were correctly classified.