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.     

Anadromous trout threatened by whitefish gill‐net fisheries in the northern Baltic Sea

We estimated the effect of the gill‐net fisheries targeted at whitefish (Coregonus sp.) on anadromous sea trout, Salmo trutta, in the Gulf of Bothnia, Baltic Sea using separate data for fish species. The analysis of sea trout captures was based on tagging and recapture data collected in 1998–2011, while whitefish data were derived from individual samples of commercial fisheries from the same period. The mesh sizes used in gill‐net fishing and the seasonal and temporal distributions of recaptured sea trout and sampled whitefish were compared in the northern and southern Gulf of Bothnia. The trout had typically spent 1–2 years at sea, and they were mainly immature with a median body length of 40–43 cm at the time of recapture in gill nets. Despite the increase in the minimum permitted landing size from 40 to 50 cm in 2008, the median length of recaptured trout remained unchanged during the study period. Most (59%) of the gillnetted trout were caught in the southern Gulf of Bothnia in gill nets with mesh sizes of 40–45 mm, which were also used in the whitefish fishery (72%). In the northern Gulf of Bothnia, nets with a smaller mesh size of 25–39 mm took 83% of the whitefish catch and 39% from recaptured trout. In both areas, the overlap in mesh sizes used to gill‐net catch whitefish and sea trout increased during the study period. There were clear seasonal and areal differences in the relative probability of sea trout being captured in gill nets, suggesting that carefully tailored spatial and temporal restrictions on gill‐net fisheries could provide a tool to protect young sea trout without causing intolerable difficulties for the fisheries targeting other species.     

Eradication of Nonnative Fish by Gill Netting from a Small Mountain Lake in California

Nearly all mountain lakes in the western United States were historically fishless, but most now contain introduced trout populations. As a result of the impacts of these introductions on ecosystem structure and function, there is increasing interest in restoring some lakes to a fishless condition. To date, however, the only effective method of fish eradication is the application of rotenone, a pesticide that is also toxic to nontarget native species. The objective of this study was to assess the effectiveness of intensive gill netting in eradicating the trout population from a small subalpine lake in the Sierra Nevada, California. We removed the resident trout population and a second trout population accidentally stocked into the study lake within 18 and 15 gill net sets, respectively. Adult trout were highly vulnerable to gill nets, but younger fish were not readily captured until they reached approximately 110 mm. To determine the utility of gill netting as a fish eradication technique in other Sierra Nevada lakes, we used morphometry data from 330 Sierra Nevada lakes to determine what proportion had characteristics similar to the study lake (i.e., small, isolated lakes with little spawning habitat). We estimated that gill netting would be a viable eradication method in 15–20% of the high mountain lakes in the Sierra Nevada. We conclude that although gill netting is likely to be more expensive and time consuming than rotenone application, it is a viable alternative under some conditions and should be the method of choice when sensitive native species are present.     

The energy budget of the brown trout population of øvre Heimdalsvatn

Energy pathways of a natural brown trout Salmo trutta population were constructed. The main subjects taken into account were: the biomass, calorific values and production of the population, natural mortality and annual yield, energy intake, calorific values and composition of the food, efficiency of food absorption, spawning and migration of young trout. The specific energy value of trout increased with increasing weight of the fish. An energy decrease of almost 50% was demonstrated for the spawning trout of both sexes, and the calorific values prior to spawning were not reached before the next summer. Energy intake was estimated to 6.87, 10.31, 8.42 and 9.15 kcal m⁻² lake surface for the years 1969, 1970, 1971 and 1972 respectively. Although a great number of food items were found in the trout stomachs, the four groups Gammarus lacustris, Lepidurus arcticus , Trichoptera and Chironomidae accounted for 2/3 of the total consumption. The efficiency of food absorption varied between 42 and 53%. The mean age of trout entering the lake from the nursery streams was ca. 3 yr. The annual amount of this immigration was estimated to be 0.28 and 0.24 kcal m⁻² lake surface for 1969 and 1970 respectively. Annual production of trout in the take was estimated to be 1.46 and 2.66 kcal m⁻² respectively for the same years. For both these years balance was found between biomass at the beginning of the year plus immigration of young and total production, minus catch by man, natural mortality and spawning on the one hand and biomass at the end of the year on the other hand.     

The population density, growth rate and production of bream, Abramis brama, in Tjeukemeer, the Netherlands

A method of estimating the population density of bream in Tjeukemeer (21.3 km²) using 16 690 introduced fish (fin-clipped and opercular tagged) is described. Gill nets of the winter fishery proved to be a more effective method of sampling the population for marked fish than fyke nets. The population density of bream (⋝25 cm) was estimated to be 180 000. There was no significant difference between the estimates derived from fin-clipped and opercular tagged fish. The growth rate of bream in Tjeukemeer (L_∞=41 cm) is poor compared with that of bream in other waters, due to its high density and the scarcity of zoobenthos available to it.
The production of bream (I–XV) is estimated to be 34 kg ha⁻¹ of which 25% is contributed by two (1959, 1963) strong year classes. Of a total biomass of 37.5 kg ha⁻¹ available to the fishery in 1969 only 2.7 kg ha^−l was removed as yield. The average P/B ratio for the population was low (0.39). It is concluded that a major flow of energy to bream is through zooplankton.     

Evaluation of the contribution of supplemental plantings of brown trout Salmo trutta (L.) to a self-sustaining fishery in the Sydenham River, Ontario, Canada

An autumn planting of 4000 tagged yearling brown trout Salmo trutta (L.) in 1969 resulted in an over-winter survival of 26%, an angler recovery the following year of 8·1 % and made up 22 % of the March, 1970 standing population of the species. August standing populations of brown trout increased from 142 trout/ha (17·6 kg/ha) in 1969 to 360 trout/ha (39·3 kg/ha in 1970 while angler harvest of the species increased from 61 trout/ha (12·7 kg/ha) at a rate of 0·26 fish/h to 89 trout/ha (18·5 kg/ha) at a rate of 0·34/h. Using angler recovery and standing population as criteria the planting contributed substantially to the fishery. Actual contribution of stocked trout however, is questioned after detailed analysis of resident population structure and the potential of natural recruitment. It is suggested that the true benefit of stocked trout may be measured by the presence of those stocked fish in excess of the number of resident trout of that size predictable from a normal length distribution curve in waters with self-sustaining populations. Complexities in evaluating the merits of supplemental plantings of hatchery-reared brown trout to existing stream fisheries are examined.     

Growth, survival and production of juvenile salmon and trout in a Scottish stream, 1966–75

Investigations of the growth, survival and production of young salmon Salmo salar , brown trout and sea trout S. trutta in sections of a stream in Scotland were made during 1966–75. At the end of the growing season, in autumn, the size of the 0+ salmon ranged from a mean weight of 1.12 g in 1966 to 2.82 g in 1973, and the size of the 0+ trout ranged from a mean of 2.20 g in 1966 to 3.56 g (68.0 mm) in 1974. Growth rates of 0+ salmon between July to September were similar from year to year, as was the case with the 0+ trout. The greater size attained in their first year by trout, resulted from the longer feeding season, provided by earlier emergence of fry and ability to continue growing in colder weather in autumn. The lengths attained by 0+ salmon and 0+ trout in September were related to the population densities of 0+ salmon and the number of days above 0° C from 1 December. There was no discernible relationship between lengths of 0+ trout and the population densities of 0+ trout. Salmon and trout lost weight during the winter, which was made up by April. The densities of 0+ salmon in June varied between 2–12m ^–2. Rates of decrease of the population densities in their first year were related to their densities at the beginning of the season, and, more closely, to the densities of salmon and trout combined. At the end of the second year's growth there were between 0.06 and 0.25 salmon m ^–2. Size of the trout populations varied less from year to year than those of salmon. The life of a year class of salmon and trout could be divided into several stages characterized by different rates of decrease of the population.     

Direct estimates of the selectivity of a multimesh and a series of single gillnets for brown trout

Hatchery brown trout Salmo trutta (1406) of length 5–20 cm were released into a 7.5 ha shallow lake. They were recaptured with 28 multimesh gillnets of a type proposed for use in the Nordic countries and 42 single gillnets of mesh size 8–22 mm (knot to knot). Corrected for the effect of different twine thicknesses, the single nets showed the highest selectivity for 16.5 mm and smaller meshes and the multimesh nets for the larger meshes. The height of the selectivity curves increased exponentially with mesh size, and most distinctly for the multimesh nets. Over a limited range of mesh sizes the selectivity of the two types of net did not differ much. Extended over mesh sizes 10.0–55.0 mm, the catching abilities of the two types of net became considerably different.     

Some characteristics of a pike Esox lucius L. population in an Irish reservoir

A study of a stocked upland reservoir trout fishery, using gill nets, revealed the presence of a large stock of pike and poor trout numbers. The overall growth rate of pike was slow. Two year-classes of pike dominated, but the broad age and length frequency ranges, and the high average weight of individuals were indicative of an unexploited stock. Higher than normal water levels during the spawning period and into the summer period in both 1985 and 1986, coincided with the dominant pike year-classes recorded several years later. This revised version was published online in July 2006 with corrections to the Cover Date.     

Induction, isolation and a characterization of the lipid content of plasma vitellogenin from two Salmo species: rainbow trout (Salmo gairdneri) and sea trout (Salmo trutta)

Vitellogenin synthesis is induced in juvenile rainbow trout (Salmo gairdneri) and juvenile sea trout (Salmo trutta) by estradiol-17 beta. A purification procedure for vitellogenin from trout plasma by precipitation with MgCl2-EDTA and subsequent anion exchange chromatography on DEAE-Sephacel is described. The total lipid contents of purified rainbow trout and sea trout vitellogenins are 18 and 19%, respectively. Approximately 2/3 of the lipids are phospholipids, while the remainder consists of triglycerides and cholesterol. Phosphorus determinations on delipidated vitellogenin yield a phosphorus content of 0.63% in rainbow trout and 0.58% in sea trout vitellogenin. Native (dimeric) vitellogenins from rainbow trout and sea trout both have an apparent molecular weight of 440,000, when estimated by gel filtration on Sepharose 6B.     

Population dynamics of Gila trout in the Gila River drainage of the south-western United States

In some small, often unstable, streams of the Gila River drainage, New Mexico, Gila trout Oncorhynchus gilae populations fluctuated numerically seasonally and annually. Few differences were noted in length-weight and size-structure comparisons, but Fulton condition index varied significantly. Time of sample and time since disturbance (natural or human-caused) were often associated with differences in condition. Other factors may include availability of prey, cannibalism, and reproductive condition. The repeatedly sampled McKnight Creek population illustrated the resilience of Gila trout populations to natural disturbances. A scouring flood in 1988 caused a >90% reduction in numbers, but, by 1992, population structure was not substantially different from that of other streams. Likewise, juvenile/adult ratio, density, and per cent large specimens (≥ 200 mm total length) of most other samples were within the ranges for the McKnight Creek population. Gila trout density (no. fish min⁻¹ electrofishing) tended to increase with higher elevation and greater drainage density (stream km catchment⁻¹ km⁻²) but decreased with larger catchments. Information gained in this study demonstrates that a variety of factors must be considered when evaluating the relative well-being of Gila trout populations and illustrates the importance of larger, more hydrologically complex drainages to the long-term survival of Gila trout populations.     

Assessment and control of non‐indigenous brown bullhead Ameiurus nebulosus populations using fyke nets in shallow ponds

In order to evaluate fyke nets as a tool for population assessment and mass removal of brown bullhead Ameiurus nebulosus populations, small, shallow ponds were sampled during late summer in 1999 and 2000. Catch efficiency, species and size selectivity of fyke nets were investigated with the mark‐recapture method. Two different strategies were applied: (1) on six occasions, the mark‐recapture method was applied to entire populations, and (2) in six other cases, sampling was done in two replicated enclosed areas (625 m²). When applied to entire populations, fyke nets were found to be size selective, and capture efficiency significantly increased with standard length. Conversely, no size selectivity of fyke nets was found in enclosed areas. Sampling in replicated enclosures yielded reproducible estimates of population density and biomass. The results suggest that double fyke nets, when combined with the mark‐recapture technique, are a very useful tool for the efficient and reliable assessment of brown bullhead populations. The results of the study also suggest that double fyke nets may potentially be a cost‐effective tool for the mass removal of non‐indigenous brown bullhead populations.     

Evaluating catches of salmonids taken by gillnets

Data from 10 185 gillnetted brown trout ( Salmo trutta L.) and 5777 Arctic charr [ Salvelinus alpinus (L.)] were analysed. Relative to mesh size, the most efficiently caught fish length (the modal length) was somewhat larger with floated nets than with smaller nets placed on the bottom. There were no such consistent differences between the two species. Fish that exceeded the modal lengths were caught more efficiently than smaller fish. The relationship of most efficient mesh size to fish length and condition factor fitted excellently to a linear equation. Based on this equation, the selectivity curve for Arctic charr gillnetted in the Nesjø reservoir, the different efficiency of nets of 0.1 and 0.17mm twine and an equation expressing the increasing height of the selectivity curve with increasing mesh size, a model is presented to compare length frequencies and total numbers of gillnet catches taken with any combination of mesh sizes.     

The ghost of hybrids past: fixation of arctic charr (Salvelinus alpinus) mitochondrial DNA in an introgressed population of lake trout (S. namaycush)

Complete fixation of arctic charr ( Salvelinus alpinus ) mitochondrial DNA (mtDNA) was observed in a southern Québec population of lake trout ( S. namaycush ). This introgressed population otherwise appeared to be normal with regard to lake trout morphology and three species-diagnostic microsatellite loci. Arctic charr do not occur in the area, suggesting that the hybridization event was prehistoric. Of several possible hypotheses, the most plausible explanation for this aberrant population is that hybridization occurred in situ soon after deglaciation, with repeated backcrossing of hybrids with lake trout. Fixation of S. alpinus mtDNA in the population may have occurred either by chance (drift) or selection, although indirect evidence and data from similarly introgressed brook trout ( S. fontinalis ) populations in the region suggest that selection favouring the S. alpinus mitochondrial type and/or associated nuclear genes may have been involved.     

Estimating the long-term effects of stocking domesticated trout into wild brown trout (Salmo trutta) populations: an approach using microsatellite DNA analysis of historical and contemporary samples

Indigenous salmonid fish gene pools are affected by domesticated conspecifics, derived from aquaculture escapes and deliberate releases. Variability was examined at nine microsatellite loci in order to assess the long-term impact of stocking domesticated trout in two brown trout populations. The study was based on analysis of two historical samples (1945-56), represented by old scale collections, and seven contemporary samples (1986-2000). In one population historical and contemporary samples were remarkably genetically similar despite more than a decade of intense stocking. Estimation of admixture proportions showed a small genetic contribution from domesticated trout (approximately 6%), and individual admixture analysis demonstrated a majority of nonadmixed individuals. The expected genetic contribution by domesticated trout was 64%, assessed from the number of stocked trout and assuming equal survival and reproductive performance of wild and domesticated trout. This demonstrates poor performance and low fitness of domesticated trout in the wild. In another population there was a strong genetic contribution from domesticated trout (between 57% and 88% in different samples), both in samples from a broodstock thought to represent the indigenous population and in a sample of wild spawners. Survival of domesticated trout and admixture with indigenous fish in the broodstock and subsequent stocking into the river, combined with a low population size of native trout relative to the number of stocked trout, could explain the observed introgression. Few nonadmixed individuals remained in the introgressed population, and I discuss how individual admixture analysis can be used to identify and conserve nonintrogressed remains of the population.     

Experimental sea ranching of brook trout, Salvelinus fontinalis Mitchill

An experiment to induce anadromy in a population of wild brook trout, Salvelinus fontinalis , was conducted near Sept-Iles, Quebec, in 1978–1979. Brook trout were captured from the Matamek River, tagged and transported to the Matamek River estuary during late spring and early summer, and allowed free movement between an impassable waterfall 0.7 km upstream and the sea. Fish were recaptured in autumn as they returned to fresh water. Over two years, 34.0% of the released fish were recaptured. Best returns were in the 2+ and 3+ age classes with 38.0 and 62.1% recaptured, respectively. Straying of transplanted fish appeared to be <1%. All age classes included sea run brook trout (sea trout) but the largest percentages of sea trout occurred in older fish. Growth was better in sea trout than in fish which did not develop anadromy, presumably a function of an increased food supply at sea. Severe tagging effects stunted growth and probably suppressed anadromy, especially among younger fish. Sexual characteristics of recaptured fish indicated suppressed maturation of gonads in sea trout compared to fish remaining in fresh water and there was a shift to a larger percentage of females in the sea trout. Comparisons between our results and data on other anadromous Salvelinus species underscore the potential for sea-ranching of trout and char as a moderate effort, high yield aquaculture technique.     

The critical-period concept for juvenile survival and its relevance for population regulation in young sea trout, Salmo trutta

An example of density-dependent regulation is provided by a long-term investigation (1966-present) of a population of migratory trout (estuarine and sea trout), Salmo trutta L., in a Lake District stream. Evidence for the concept of a critical period for the survival of young fish is briefly reviewed and found to be rather equivocal. The concept is, however, relevant to the trout population. Loss rates were high before but low after a critical survival time ( t_c days after fry emergence) that varied between year-classes (range 33-70 days) and was inversely density-dependent on egg density. Survivor density and loss rates were strongly density-dependent on egg density before t _c, but proportionate survival with stable loss-rates occurred after t _c. Some trout established feeding territories soon after emergence and the number of fish without territories decreased from a high initial value to a negligible value at t _c. Fish size at t_c was not constant but increased as t _c increased. The range of t _c for the different year-classes was similar to that for survival times of unfed fry in the laboratory. A new stock-recruitment model, incorporating t _c, has been developed for the trout population and shown to be related to the model (Ricker curve) used in the long-term study. The critical time can also be regarded as the critical age for survival in young trout; this concept may be relevant to other fish species.     

Effects of species invasion on population dynamics,vital rates and life histories of the native species

Invasions occurring in natural environments provide the opportunity to study how vital rates change and life histories evolve in the presence of a competing species. In this work, we estimate differences in reproductive traits, individual growth trajectories, survival, life histories and population dynamics between a native species living in allopatry and in sympatry with an invasive species of the same taxonomic Family. We used as a model system marble trout Salmo marmoratus (native species) and rainbow trout Oncorhynchus mykiss (non-native) living in the Idrijca River (Slovenia). An impassable waterfall separates the stream into two sectors only a few 100 meters apart: a downstream sector in which marble trout live in sympatry with rainbow trout and an upstream sector in which marble trout live in allopatry. We used an overarching modelling approach that uses tag-recapture and genetic data (>2,500 unique marble and rainbow trout were sampled and genotyped) to reconstruct pedigrees, test for synchrony of population dynamics and model survival and growth, while accounting for individual heterogeneity. The population dynamics of the two marble trout populations and of rainbow trout were synchronous. We found higher prevalence of younger parents, higher mortality and lower population density in marble trout living in sympatry with rainbow trout than in marble trout living in allopatry. There were no differences in the average individual growth trajectories between the two marble trout populations. Faster life histories of marble trout living in sympatry with rainbow trout are consistent with predictions of life history theory.     

Comparison of brook trout reproductive success and recruitment in an acidic adirondack lake following whole lake liming and watershed liming

Limestone applications to the catchment of one tributary to Woods Lake were highly effective in reducing stream acidity and stabilizing seasonal fluctuations in pH. The resulting improvement in stream water quality also led to a dramatic shift in reproductive strategy of the Woods Lake brook trout population. Prior to catchment liming, brook trout in Woods Lake were restricted to spawning on poor quality near shore substrate with limited ground water seepage. Reproductive success was limited by high mortality of eggs and larvae and recruitment from in lake spawning was not successful. Spawning brook trout did not utilize the tributary for spawning prior to watershed liming. Mitigation of acidity in the tributary, by catchment liming, effectively extended the spawning habitat available to the Woods Lake brook trout population and one year following treatment brook trout spawned successfully in the tributary for the first time in 6 years of observation. Significant recruitment of young trout into the lake population occurred from 1991 through 1993, although the absolute number of fish captured was relatively small. In the fall of 1993, four year classes of naturally spawned brook trout were present in the lake. Although reproductive success was enhanced by improving tributary spawning habitat in the Woods Lake basin, self maintenance of the population may be limited by low recruitment rates of young trout, due to high levels of summer mortality resulting from predation. Mitigation of this constraint would require substantially higher levels of fry production than were observed in Woods Lake and/or enhanced refugia for young trout. The results of this experiment suggest that re-establishment of tributary spawning populations of brook trout may be possible, with future reductions in acidic deposition, in acidic Adirondack lakes with limited in-lake spawning habitat.     

Production of salmon and trout in a stream in Scotland

For three years the population size, rates of growth, standing stock, production and yield of all year classes of salmon and trout within three sections of a stream in Scotland were studied. Total salmon production as fresh weight per m² was 6.5 g in 1966, 10.6 g in 1967 and 11.1 g in 1968, and total trout production was 10.3g in 1966, 12.3 g in 1967 and 7.7g in 1968. Fish of 0+ and 1+ year old provided usually more than 90% of the total annual salmon production and 80 % of the annual trout production. Yield of salmon smolts (about 9 cm or longer after 2 years growth) per m² was 0.10 in 1966, 0.22 in 1967 and 0.15 in 1968. The smolt yield by weight was 29 % of the production of the 1966 year class of salmon and 16% of the 1967 year class. Numbers of trout of 9 cm or longer produced in the same time were higher and their weight was 60% of the total production of the 1966 year class and 32% of the 1967 year class.