Increased growth and recruitment of piscivorous perch, Perca fluviatilis, during a transient phase of expanding submerged vegetation in a shallow lake

1. In this study, we examine how a 7‐year period of expanding submerged stonewort (Chara spp.) vegetation during a shift from turbid to clear water in a shallow lake influenced individual growth and population size structure of perch (Perca fluviatilis). We expected that a shift from phytoplankton to macrophyte dominance and clear water would improve feeding conditions for perch during a critical benthivorous ontogenetic stage, and enhance the recruitment of piscivorous perch. 2. Growth analysis based on opercula showed that growth during the second year of life was significantly higher in years with abundant vegetation than in years with turbid water and sparse vegetation. Growth was not affected during the first, third and fourth year of life. Stable isotope analyses on opercula from 2‐year‐old perch showed that the increase in growth coincided with a change in carbon source in the diet. Stable nitrogen ratio did not change, indicating that the increased growth was not an effect of any change in trophic position. 3. Following the expansion of submerged vegetation, perch size range and abundance of piscivorous perch increased in central, unvegetated areas of the lake. In stands of stoneworts, however, mainly benthivorous perch were caught, and size range did not change with time. 4. Our findings provide empirical support for the notion that establishment of submerged vegetation may lead to increased recruitment of piscivorous perch, because of improved competitive conditions for perch during the benthivorous stage. This is likely to constitute a benthic‐pelagic feedback coupling, in which submerged vegetation and clear water promote the recruitment of piscivorous perch, which, in turn, may increase water clarity through top‐down effects in the pelagic.     

Impact of Juvenile Stocking Size on the Major Carp Production in a Minor Reservoir,Bibinagar, India

The present study deals with the impact of juvenile stocking sizes of the major carp on production in a minor reservoir, Bibinagar, Nalgonda, India. Reservoir surface area equaled over 23.8 ha and water from the reservoir was used for irrigation and fisheries. Four experiments were conducted for 4 years from 2000–2001 to 2003–2004. The experiments were planned in such a way that every year juvenile stocking size was held constant and subsequent fish production analyzed. During the first year’s experiment (2000–2001) a stocking size of 25–30 mm (fry) was maintained. Similarly 50–55 (advanced fry), 75–80 mm (fingerling) and 100–105 mm (advanced fingerling) were stocked during 2001–2002, 2002–2003 and 2003–2004 respectively. Uniform yearly stocking densities (2000/ha) were established in each experiment in the month of July and fish were harvested in June of the subsequent year. Major carp production was enhanced with larger stocking size. Yearly productions equaled 144.00, 231.48, 632.91 and 1005.03 kg/ha/year with the above stocking sizes. Variation in stocking sizes had significant (P<0.05) effects on fish production. The number of fish per kg production decreased gradually with increases in stocking size with an average value of 3.97. Reservoir production of catla was the most abundant species, followed by rohu, common carp, mrigal and grass carp. These results show that stocking size has a great impact on fish production and the stocking of advanced fingerlings will provide maximum carp production in minor reservoirs in India.     

Ontogenetic variation in density‐dependent growth of brown trout through habitat competition

1. Density‐dependent growth has been widely reported in freshwater fishes, but the ontogenetic evolution of competition and its subsequent effects on growth through a life span remains unclear. 2. Patterns of competition can be described by integrating population abundance data with habitat‐modelling results. Weighted usable area (WUA; m² WUA ha^?1) curves are obtained for each flow value and are then coupled with demographic data to obtain the occupancy rates (trout m^?2 WUA, the density of a given age class related to its suitable habitat) of the WUA for every age class, year and site. 3. We examined a long‐term data series searching for temporal variation in the influence of habitat occupancy rate on the growth of brown trout Salmo trutta. We tested whether (i) mean cohort mass (mean mass of the cohort during the first 3 years of life) is affected by the occupancy rate experienced across a life span; and (ii) the occupancy rate experienced at different ages influenced mean body size. 4. We observed a consistent negative power relationship between average cohort mass and mean occupancy rate through a life span, indicating that stronger cohorts were related to a reduced growth, with likely consequences for individual fitness. 5. The effects of occupancy rate on size‐at‐age were mainly detected in the size attained at the second year of life, but they were because of the competition at different times. Thus, the level of competition varied through ontogeny, in some of the rivers affecting growth since the first year of life, whereas in most of the rivers the main effects on body size resulted from the competition during the second year of life. 6. Occupancy rate appears more appropriate than density for assessing the occurrence of habitat competition in freshwater fishes, since it encompasses the differences in quantity and quality of suitable habitat for each age class. 7. Our study highlights the importance of density‐dependent growth as a key process in the dynamics of brown trout populations, its temporal variation depending on the temporal changes of density and the variation of competition associated with the habitat capacity for each life stage.     

Cohort‐specific estimates of first‐year survival are positively associated with size at stocking for lake sturgeon Acipenser fulvescens (Rafinesque 1817) stocked in Black Lake,Michigan, USA

The authors conducted a gillnet survey in 2013 in Black Lake, Michigan, USA to evaluate the lake sturgeon (Acipenser fulvescens) stocking programme that began in 2001. Objectives were to (i) estimate year‐class specific abundance of juvenile lake sturgeon in Black Lake; and (ii) determine year‐class specific survival of stocked year classes and determine whether year‐class‐specific first‐year survival was related to average size at the time of stocking. Deployed were 15 and 20 cm stretch mesh gillnets at 72 randomly selected sites in Black Lake over a 3‐week survey using a Schnabel multiple‐mark, multiple‐recapture estimator to determine overall abundance of stocked fish. Ages for captured fish were determined from fin ray cross sections and the presence of coded wire tags, and apportioned the overall abundance estimate of juveniles to year class using an age‐length key. Overall survival estimates were calculated by dividing the year‐class specific abundance estimates by the number of fish stocked that year. Also evaluated was the relationship between first‐year survival and average total length (TL) at time of stocking using logistic regression. Overall survival from stocking to 2013 ranged from 0.03 to 0.53. First‐year survival was positively associated with average TL at stocking, and ranged from 0.05 for fish stocked at 9 cm TL to 0.84 for fish stocked at 22 cm TL. Estimation of future cohort‐specific abundance based on size‐based expected survival allows managers to establish annual stocking targets that should lead to the achievement of long‐term population goals for adult abundance.     

Population cycles and changes in body size of the lynx in Alaska

The lynx Lynx canadensis is a common predator in the boreal forests of North America. Its population fluctuates during a 9- to 11-year cycle in synchrony with the population size of its main prey, the snowshoe hare Lepus americanus. Using adult museum specimens, we studied changes in skull (and hence body) size of the lynx in Alaska during the second half of the 20th century. The population cycle in Alaska averaged 9 years, similar to that reported in the neighbouring Yukon. Using harvest data of lynx as an estimate of population size, we found that skull size was negatively related to population size. This relationship was strongest not for the population density in the year of death (X), but for year X-3, a carry-over effect from the first year (or years) of life, indicating that conditions during the fast-growth years are determining body size. We suggest that the density-dependent effect is probably due to changes in food supply, either resulting from the adverse effects of competition or a possible diminished availability of food. Two skull parameters decreased significantly during the second half of the 20th century. We do not know the cause for the year effect and suggest that it might be due to a long-term change in the availability of prey. Canine size did not change during the study period, probably an indication that snowshoe hares maintained their status as the main prey of the lynx throughout the study period. Electronic supplementary material The online version of this article (doi:) contains supplementary material, which is available to authorized users.     

Carbon and nitrogen partitioning in the biennial monocarp Arctium tomentosum Mill

Summary Growth and nitrogen partitioning were investigated in the biennial monocarp Arctium tomentosum in the field, in plants growing at natural light conditions, in plants in which approximately half the leaf area was removed and in plants growing under 20% of incident irradiation. Growth quantities were derived from splined cubic polynomial exponential functions fitted to dry matter, leaf area and nitrogen data.Main emphasis was made to understanding of the significance of carbohydrate and nitrogen storage of a large tuber during a 2-years' life cycle, especially the effect of storage on biomass and seed yield in the second season. Biomass partitioning favours growth of leaves in the first year rosette stage. Roots store carbohydrates at a constant rate and increase storage of carbohydrates and nitrogen when the leaves decay at the end of the first season. In the second season the reallocation of carbohydrates from storage is relatively small, but reallocation of nitrogen is very large. Carbohydrate storage just primes the growth of the first leaves in the early growing season, nitrogen storage contributes 20% to the total nitrogen requirement during the 2nd season. The efficiency of carbohydrate storage for conversion into new biomass is about 40%. Nitrogen is reallocated 3 times in the second year, namely from the tuber to rosette leaves and further to flower stem leaves and eventually into seeds. The harvest index for nitrogen is 0.73, whereas for biomass it is only 0.19.     

Seasonal growth,density, reproductive phenology and agar quality of Gracilaria sordida (Gracilariales,Rhodophyta) at Mokomoko Inlet,New Zealand

Growth of mesh-enclosed Gracilaria sordida plants was determined monthly for one year at the Mokomoko mudflat, South Island, New Zealand. Growth of plants with permanent water cover was correlated with water temperature and was most rapid during summer months. Plants exposed at low tide grew only during early spring and late autumn. Bimonthly quadrat sampling of a mudflat population showed that all stages of the life cycle were present throughout the year. Spermatangial plant length and biomass were greatest in early spring; cystocarpic and tetrasporic plants were greatest in midsummer. Sterile plants were most numerous in the late summer. Agar yield showed little variation either seasonally or between different stages of the life cycle. Agar gel strengths for all life cycle stages were greatest at the time of peak plant size and abundance. Gels from spermatangial plants generally were weaker than those from other stages.     

Early social status and the development of life-history strategies in Atlantic salmon

Atlantic salmon have a variable life cycle. In good growing conditions, underyearling fish may metamorphose into the migratory smolt phase during their second spring, or delay at least a further year. The strategy adopted by particular fish appears to become fixed during their first summer. This paper examines whether either feeding efficiency or dominance in mid-summer correlates with the life-history strategy adopted. Eighty fish were individually marked and their feeding efficiency (= mean handling time for food items) and dominance rank measured under laboratory conditions in mid-July. Growth rates of the fish were then monitored over the next three months, until developmental strategies became apparent. Discriminant and logistic regression analyses revealed that both dominance rank and size attained by July were independent, significant predictors of future developmental pattern (the age at metamorphosis being correctly predicted on the basis of rank and size in 84% of cases) whereas feeding efficiency had no effect. Thus fish that were dominant or larger two months after first feeding or both had a greater probability of migrating after only one year in freshwater than those more subordinate or smaller or both.     

The growth and reproductive strategy of the gudgeon, Gobio gobio (L.), in two hard-water rivers in southern England

Scales from 682 gudgeon from the River Frome and 504 from the River Stour were used for age determinations. Growth in length was confined to the period May to October, but some weight increase occurred during the winter because of gonad development. Growth rates in the two rivers were the same, and were higher than most of those reported from other European rivers. Wide fluctuations, up to 12-fold, occurred in the year-class strengths of Frome gudgeon, caused by variations in the survival of juvenile gudgeon in their first year of life. Density-independent factors, particularly water temperature, were major influences. Female gudgeon grew marginally slower than the males, but they matured earlier and at a smaller size. They were fractional spawners but their total reproductive effort each season was high. Both sexes had low survival rates and their reproductive life spans were rarely more than three years. These life history traits support the premise that these gudgeon populations are r-selected.     

Testing mate choice and overdominance at MH in natural families of Atlantic salmon Salmo salar

This study aimed to test mate choice and selection during early life stages on major histocompatibility (MH) genotype in natural families of Atlantic salmon Salmo salar spawners and juveniles, using nine microsatellites to reconstruct families, one microsatellite linked to an MH class I gene and one minisatellite linked to an MH class II gene. MH‐based mate choice was only detected for the class I locus on the first year, with lower expected heterozygosity in the offspring of actually mated pairs than predicted under random mating. The genotype frequencies of MH‐linked loci observed in the juveniles were compared with frequencies expected from Mendelian inheritance of parental alleles to detect selection during early life stages. No selection was detected on the locus linked to class I gene. For the locus linked to class II gene, observed heterozygosity was higher than expected in the first year and lower in the second year, suggesting overdominance and underdominance, respectively. Within family, juveniles' body size was linked to heterozygosity at the same locus, with longer heterozygotes in the first year and longer homozygotes in the second year. Selection therefore seems to differ from one locus to the other and from year to year.     

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.     

Migration, growth and survival of wild and hatchery-reared anadromous Arctic charr (Salvelinus alpinus) in Finnmark, Northern Norway

Two groups of anadromous Arctic charr ( Salvelinus alpinus ) (size 200–350 mm) reared in heated water (6–12° C) under simulated natural photoperiod were individually tagged and released in spring 1988. The fish were released at two sites, in the estuary of the River Halselva and in the fjord, 2 km from the river mouth. Growth, timing of migration and survival of these hatchery-reared fish was compared to that of wild anadromous charr of the same size over a 4-year period. The hatchery-reared charr had poorer growth than the wild fish during their first year in sea water. They also resided longer in the sea and had a slightly lower survival than wild fish. During the second year, hatchery-reared charr displayed good growth, and after the third sea-season the fish were ready for slaughter at a size of approximately 800g. The results suggest that the successful development of Arctic charr ranching will be dependent upon production and release strategies that lead to improved migratory and feeding behaviour of the fish during their first season at sea.     

Validation and implications of a growth model for brown trout, Salmo trutta, using long-term data from a small stream in north-west England

Summary 1. The objectives were: (i) to check the validity of a new growth model; (ii) to examine the relationship between population density and both mean mass and mean growth rate and (iii) to discover if compensatory growth occurred. First (0+) and second (1+) year‐old juvenile sea‐trout were sampled by electrofishing at the beginning and end of the summer from 1967 to 2000. Additional samples were taken in some years in winter and in the critical period for survival when the fry first emerge from the gravel. The trout left the stream as pre‐smolts in May, soon after their second birthday. 2. A growth model ( Elliott, Hurley & Fryer, 1995 ) estimated the mean mass of the trout over the 2 years spent in fresh water. The date and mean mass at the start of the growth period were defined as the median date for fry emerging from the gravel and their mean mass at emergence, both being estimated from individual‐based models ( Elliott & Hurley, 1998a, b ). 3. The variation in mean mass among year‐classes was small for newly‐emerged fry (CV = 6.2%), maximum at the start of the first summer of the life cycle (CV = 38.1%), and then decreased gradually for successive life‐stages to a low value for pre‐smolts (CV = 10.8%). Mean mass was not related to population density and, therefore, mean growth rate was density‐independent. Growth in the first, but not the second, winter of the life cycle was lower than model prediction, but when it was assumed in the model that there was no first‐winter growth, there was good agreement in most year‐classes between model estimated values and observed mean mass. Exceptions were that mean masses and growth rates for 0+ trout after four summer droughts were lower than expected, but compensatory growth followed, so that observed and expected masses were similar for 1+ trout. 4. Pre‐smolt mean mass on 30 April measured total growth achieved in the freshwater phase of the life cycle. This was significantly related to mean mass at the end of the first and second summers of the life cycle, but not to the emergence date and mean mass of emerging fry. 5. These juvenile sea‐trout were growing at their maximum potential in most year‐classes but when this was not achieved, compensatory growth soon restored their mass to values expected from the model. This ensured a low variation in the mean mass of pre‐smolts just before they migrated to the sea. However, the latter mass was higher in more recent year‐classes (1987–98) than in previous ones (1967–86), demonstrating the effect of slightly higher stream temperature. This study has shown the importance of developing realistic growth models in order to detect departure from maximum potential growth, and the more subtle effects of temperature change, possibly due to the effects of climate change.     

The survival, growth and diet of pike fry, Esox lucius L., stocked at different densities in experimental ponds

Yolk-sac pike fry were stocked at densities of 0.74 – 81.4 m⁻² in two ponds, each divided into eight sectors (mean area 155.8 m²). Growth and survival were recorded from May to December 1985. The growth rates were variable within each sector. The size-range of sampled fish increased throughout the year, but showed no significant correlation with density. Fry survival was initially density-independent but switched by late June/July to density-dependence, ranging from 0.5 to 43.6% of initial stocking numbers. The highest mean daily mortality rates occurred during May-July. The final survival in December ranged between sectors from 0.059 to 11.25% of the starting stock densities. The final biomass per unit area of pike surviving in December was not related to initial stocking density. In Pond 1 the mean biomass produced was 2.21 gm⁻² and in Pond 2 was 3.49gm⁻².
Pike fry < 30 mm fed only on invertebrates; those 30–100 mm took a wide range of invertebrates, cyprinids. sticklebacks and other pike. Cannibalism occurred at most densities between 5.45 and 81.4 fish m⁻².
Where attempts are made to increase pike production in managed populations by releasing small fry, an upper stock density of 5 fry m⁻² is advised if large, density-dependent mortalities are to be avoided.     

Effects of stocking density and food density on survival,growth and yield of laboratory-reared larvae of sea bream Archosargus rhomboidalis (L.) (Sparidae)*

Growth and survival of sea bream, Archosargus rhomboidalis (L.) larvae were affected by both abundance of eggs that were initially stocked in 75 1 rearing systems and by the concentration of copepod nauplii and copepodites that were fed to larvae. Stocking levels were 2, 4, 8,16 or 32 per litre while food abundance was maintained at approximately 100, 500, 1500 or 3000 per litre. Experiments were of 16 days duration at 26° C. Survival was best, often exceeding 60%, when food levels were 1500 or 3000 per litre and when stocking density did not exceed 8 eggs per litre. Growth was best at the lowest stocking densities and highest food levels. The highest total yields in wet weight occurred at 8 per litre stock density and 3000 per litre food level. Mean wet weight per survivor and yield per stocked egg were greatest at the lowest stocking densities and highest food levels. A 500 per litre food level was marginal for growth and survival, and 100 per litre produced significant survival only at the 2 per litre stocking density. Two experiments at 6000 and 10 000 per litre food levels at 4 per litre stock density gave the best observed growth, and survival as good as in any other experiments. Possible relations between sea bream larvae and their food supply in the natural environment are discussed. Results also are discussed in terms of their possible contribution to aquaculture efforts.     

Development of partner preferences in Japanese Macaques (Macaca fuscata): Effects of gender and kinship during the second year of life

Quantitative data are presented on the effects of subject sex, partner sex,and kinship on the social interactions of 18 juveniles of the Oregon troop of Japanese macaques (Macaca fuscata).Data on these subjects as infants were also used to detail maturational changes in partner sex preferences. Nine males and nine females, whose multiparous mothers represented a cross section of dominance ranks, were observed using a focal-animal technique. Juveniles of both sexes engaged in more proximity, contact, grooming, mounting, aggression, and social play with kin than with nonkin partners. They initiated less contact with females and more contact with males during their second year. They initiated more grooming and aggression during their second year than their first year, with females displaying a strong preference for grooming females and males specifically aggressing males more during the second year. Aggression was higher between same-sexed partners than between opposite-sexed partners. Males engaged in more social interactions with males during the second year than the first year of life. Males played more than females during both years. Males played more with males during the second year than the first year, and males played with males more than did females during the second year. We conclude that sex differences in behavioral frequencies become evident during the first year of life, and sex differences in partner preferences emerge during the second year of life.     

Ontogenetic dynamics of the shell convolution diameter of the river snail Viviparus viviparus (Gastropoda, Pectinibranchia, Viviparidae)

The dynamics of the shell convolution diameter with regard to the mollusk age was studied for the river snail Viviparus viviparus. It was found that the diameter of the first (juvenile) convolution remained constant during the ontogenetic development. A weak, but significant increase in the diameter of the second and the third shell convolutions (also juvenile) was observed during the first year of postembryonic development. The forth and the fifth shell convolutions were formed during the first year of mollusk life after hatching; their diameters increased gradually during the second year, and remained constant for the remainder of the life span.     

Population development of the mosquitofish,Gambusia affinis,in rice fields

Synopsis Development of mosquitofish,Gambusia affinis, stocks in rice fields following stocking for mosquito control is poorly understood and highly variable. To characterize population development and explain observed variability, size distributions and total numbers of mosquitofish stocks were followed from stocking through the end of the summer rice season in several experimental rice paddies. Instead of the highly variable, logistic growth implied by previous studies in which only adult fish were sampled, we observed a consistent development of size structure between years, with some variability in specific demographic processes. Population development consists of: (1) an initial peak in numbers due to a pulse of recruitment, (2) a period of low recruitment and constant or declining numbers, and (3) a second peak caused by a second pulse of recruitment. Timing of the initial peak appears to depend on rice height. Differences in the rate of decline following the peak are apparently due to different mortality rates. The second peak in reproduction is probably due to a second parturition by stocked females, possibly followed by first reproduction by young born earlier. Since population development in rice fields following stocking in the spring is similar to development of natural populations in temperate regions in which there is no reproduction during the winter, results obtained here are relevant to natural as well as artificially stocked systems.     

High stocking density during larviculture and effect of size and diet on production of juvenile Lophiosilurus alexandri Steindachner, 1876 (Siluriformes: Pseudopimelodidae)

Different stocking densities were investigated in larviculture and feeding of Lophiosilurus alexandri, as well as analyses of the effects on juveniles of two size‐classes and two different commercial formulated diets. The first experiment was two‐phased: (a) larvae stocked at densities of 60, 120, 180, 240, and 300 larvae L⁻¹ fed with Artemia nauplii and reared for 15 days; (b) in phase 2, densities of 5, 10, 15, 30, and 40 juveniles L⁻¹ were evaluated during feed training (20 days). Mean water temperature in both phases was 28°C. In the first phase of experiment 1, the different stocking densities did not affect fish growth or survival. In phase 2, growth was similar in all densities; however, survival was lower at higher densities. The increased density provided a rise in biomass and number of individuals produced in both phases. In the second experiment, two size‐classes of feed‐trained juveniles (30.22 ± 1.84 and 34.66 ± 2.41 mm) were given pellets of two different diameters (1.2 and 2.6 mm) for 20 days. The largest juveniles fed the 1.2 mm inert diet had higher final weights and lengths. Larviculture and feed training of L. alexandri can thus be performed successfully at high stocking densities of 300 larvae L⁻¹ during the first 15 days of feeding, and at densities of up to 40 juveniles L⁻¹ during the 20 days of feed training, respectively.     

Individual variation in the growth of captive infant gorillas

Serial anthropometric data were obtained during the first year of life of six nursery-reared infant gorillas in the Columbus (Ohio) Zoo. Two of the infants are likely to be monozygotic twins as determined by DNA analysis. Growth curves were fitted to serial measures of cephalo-thoracic-abdominal length, arm length, leg length, head circumference, upper arm circumference, and weight from each gorilla, to describe individual patterns of variation in skeletal growth and body composition. Growth in skeletal measures tended to be curvilinear to varying degrees over the first year of life. Body composition varied more than skeletal measures throughout the first year as a consequence of individual health status. Individual growth and body composition variations appear to reflect both genetic and environmental influences in this small sample of captive infant gorillas.