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Density-dependent Growth (density-dependent + growth)

Distribution by Scientific Domains
Life Sciences77%
Earth and Environmental Science22%

Selected Abstracts

Density-dependent growth of young-of-the-year Atlantic salmon (Salmo salar) revisited

ECOLOGY OF FRESHWATER FISH, Issue 1 2010
I. Imre
Imre I, Grant JWA, Cunjak RA. Density-dependent growth of young-of-the-year Atlantic salmon (Salmo salar) revisited. Ecology of Freshwater Fish 2010: 19: 1,6. © 2009 John Wiley & Sons A/S Abstract,,, The length of individual young-of-the-year (YOY) Atlantic salmon (Salmo salar) in Catamaran Brook decreases with increasing population density following a negative power curve. Because most of this decrease in growth rate occurs at low densities (<1 fish·m,2), (Imre et al. 2005; Journal of Animal Ecology, 74: 508,516) suggested that exploitation competition for drifting prey rather than space limitation might be responsible for this pattern. Recently, (Ward et al. 2007; Journal of Animal Ecology, 76: 135,138) showed that the negative power curve of growth rate versus density can be caused by other mechanisms and suggested that Imre et al.'s evidence for density-dependent growth would have been stronger if we had analysed final size versus initial density rather than final density. We examined (i) whether the negative power curve of size versus density was also apparent in an analysis of final size versus initial density and tested two predictions that emerge from Ward et al.'s model, (ii) the variance in body size increases with population density, and (iii) the maximum fish size at a site is density-independent. The final size of YOY salmon decreased with increasing initial density following a negative power curve. Our data did not provide strong support for the above predictions emerging from Ward et al.'s model. Our analyses of different years, sites and seasons were consistent with the hypothesis of density-dependent growth of YOY salmon. [source]

Density-dependent growth of young-of-the-year Atlantic salmon Salmo salar in Catamaran Brook, New Brunswick

JOURNAL OF ANIMAL ECOLOGY, Issue 3 2005
I. IMRE
Summary 1While density-dependent mortality and emigration have been widely reported in stream salmonid populations, density-dependent growth is less frequently detected. A recent study suggests that density-dependent growth in stream salmonids occurs at low densities, whereas density-dependent mortality and emigration occur at high densities. 2To test the hypothesis that density-dependent growth occurs primarily at low rather than at high densities, we examined the relationship between average fork length and population density of young-of-the-year (YOY) Atlantic salmon at the end of the growing season using a 10-year data set collected on Catamaran Brook, New Brunswick. We tested whether (1) average body size decreases with increasing density; (2) the effect of density on average body size is greatest at low densities; (3) growth rate will decrease most rapidly at low effective densities [,(fork length)2]; (4) density-dependent growth is weaker over space than over time; and (5) the strength of density-dependent growth increases with the size of the habitat unit (i.e. spatial scale) when compared within years, but not between years. 3There was a strong negative relationship between the average body size and population density of YOY Atlantic salmon in the autumn, which was best described by a negative power curve. Similarly, a negative power curve provided the best fit to the relationship between average body size and effective density. Most of the variation in average body size was explained by YOY density, with year, location and the density of 1+ and 2+ salmon accounting for a minor proportion of the variation. 4The strength of density-dependent growth did not differ significantly between comparisons over space vs. time. Consistent with the last prediction, the strength of density-dependent growth increased with increasing spatial scale in the within-year, but not in the between-year comparisons. 5The effect of density on growth was strongest at low population densities, too low to expect interference competition. Stream salmonid populations may be regulated by two mechanisms: density-dependent growth via exploitative competition at low densities, perhaps mediated by predator-induced reductions in drift rate, and density-dependent mortality and emigration via interference competition at high densities. [source]

Density-dependent growth in hatchery-reared brown trout released into a natural stream

JOURNAL OF FISH BIOLOGY, Issue 5 2004
L. F. Sundström
Hatchery-reared brown trout Salmo trutta stocked in a natural stream in addition to resident wild brown trout grew more slowly than those stocked with an experimentally reduced density of brown wild trout. In both cases, hatchery-reared brown trout grew more slowly than resident wild fish in control sections. Mortality and movements did not differ among the three categories of fish. The results showed that growth of stocked hatchery-reared brown trout parr was density-dependent, most likely as a consequence of increased competition. Thus, supplementary release of hatchery-reared fish did not necessarily increase biomass. [source]

Density-dependent growth of young-of-the-year Atlantic salmon (Salmo salar) revisited

ECOLOGY OF FRESHWATER FISH, Issue 1 2010
I. Imre
Imre I, Grant JWA, Cunjak RA. Density-dependent growth of young-of-the-year Atlantic salmon (Salmo salar) revisited. Ecology of Freshwater Fish 2010: 19: 1,6. © 2009 John Wiley & Sons A/S Abstract,,, The length of individual young-of-the-year (YOY) Atlantic salmon (Salmo salar) in Catamaran Brook decreases with increasing population density following a negative power curve. Because most of this decrease in growth rate occurs at low densities (<1 fish·m,2), (Imre et al. 2005; Journal of Animal Ecology, 74: 508,516) suggested that exploitation competition for drifting prey rather than space limitation might be responsible for this pattern. Recently, (Ward et al. 2007; Journal of Animal Ecology, 76: 135,138) showed that the negative power curve of growth rate versus density can be caused by other mechanisms and suggested that Imre et al.'s evidence for density-dependent growth would have been stronger if we had analysed final size versus initial density rather than final density. We examined (i) whether the negative power curve of size versus density was also apparent in an analysis of final size versus initial density and tested two predictions that emerge from Ward et al.'s model, (ii) the variance in body size increases with population density, and (iii) the maximum fish size at a site is density-independent. The final size of YOY salmon decreased with increasing initial density following a negative power curve. Our data did not provide strong support for the above predictions emerging from Ward et al.'s model. Our analyses of different years, sites and seasons were consistent with the hypothesis of density-dependent growth of YOY salmon. [source]

Density-dependent growth of young-of-the-year Atlantic salmon Salmo salar in Catamaran Brook, New Brunswick

JOURNAL OF ANIMAL ECOLOGY, Issue 3 2005
I. IMRE
Summary 1While density-dependent mortality and emigration have been widely reported in stream salmonid populations, density-dependent growth is less frequently detected. A recent study suggests that density-dependent growth in stream salmonids occurs at low densities, whereas density-dependent mortality and emigration occur at high densities. 2To test the hypothesis that density-dependent growth occurs primarily at low rather than at high densities, we examined the relationship between average fork length and population density of young-of-the-year (YOY) Atlantic salmon at the end of the growing season using a 10-year data set collected on Catamaran Brook, New Brunswick. We tested whether (1) average body size decreases with increasing density; (2) the effect of density on average body size is greatest at low densities; (3) growth rate will decrease most rapidly at low effective densities [,(fork length)2]; (4) density-dependent growth is weaker over space than over time; and (5) the strength of density-dependent growth increases with the size of the habitat unit (i.e. spatial scale) when compared within years, but not between years. 3There was a strong negative relationship between the average body size and population density of YOY Atlantic salmon in the autumn, which was best described by a negative power curve. Similarly, a negative power curve provided the best fit to the relationship between average body size and effective density. Most of the variation in average body size was explained by YOY density, with year, location and the density of 1+ and 2+ salmon accounting for a minor proportion of the variation. 4The strength of density-dependent growth did not differ significantly between comparisons over space vs. time. Consistent with the last prediction, the strength of density-dependent growth increased with increasing spatial scale in the within-year, but not in the between-year comparisons. 5The effect of density on growth was strongest at low population densities, too low to expect interference competition. Stream salmonid populations may be regulated by two mechanisms: density-dependent growth via exploitative competition at low densities, perhaps mediated by predator-induced reductions in drift rate, and density-dependent mortality and emigration via interference competition at high densities. [source]

Density-dependent mortality is mediated by foraging activity for prey fish in whole-lake experiments

JOURNAL OF ANIMAL ECOLOGY, Issue 4 2003
Peter A. Biro
Summary 1Whereas the effects of density-dependent growth and survival on population dynamics are well-known, mechanisms that give rise to density dependence in animal populations are not well understood. We tested the hypothesis that the trade-off between growth and mortality rates is mediated by foraging activity and habitat use. Thus, if depletion of food by prey is density-dependent, and leads to greater foraging activity and risky habitat use, then visibility and encounter rates with predators must also increase. 2We tested this hypothesis by experimentally manipulating the density of young rainbow trout (Oncorhynchus mykiss) at risk of cannibalism, in a replicated single-factor experiment using eight small lakes, during an entire growing season. 3We found no evidence for density-dependent depletion of daphnid food in the nearshore refuge where most age-0 trout resided. Nonetheless, the proportion of time spent moving by individual age-0 trout, the proportion of individuals continuously active, and use of deeper habitats was greater in high density populations than in low density populations. Differences in food abundance among lakes had no effect on measures of activity or habitat use. 4Mortality of age-0 trout over the growing season was higher in high density populations, and in lakes with lower daphnid food abundance. Therefore, population-level mortality of age-0 trout is linked to greater activity and use of risky habitats by individuals at high densities. We suspect that food resources were depleted at small spatial and temporal scales not detected by our plankton sampling in the high density treatment, because food-dependent activity and habitat use by age-0 trout occurs in our lakes when food abundance is experimentally manipulated (Biro, Post & Parkinson, in press). [source]

Stocking density-dependent growth and survival of Asian sun catfish, Horabagrus brachysoma (Gunther 1861) larvae

JOURNAL OF APPLIED ICHTHYOLOGY, Issue 4 2010
S. K. Sahoo
Summary The aim of the experiment was to evaluate the growth and survival of Horabagrus brachysoma larvae at different stocking densities (3, 7, 13, 20, 27 and 33 larvae L,1) during their hatchery phase. Total length and wet weight of the larvae consistently decreased (P < 0.05) at the end of 14 and 28 days of rearing as the density increased. The specific growth rate was significantly (P < 0.05) highest at three larvae L,1 compared to the other five densities. The percent weight gain and survival of larvae was also highest at lowest density. The observation corroborates that catfish larvae can be reared at low densities in stagnant water conditions. Considering the value of larval growth, survival and overall weight gain, the stocking density of seven larvae L,1 has been identified as the maximum for larval rearing of H. brachysoma under hatchery conditions. [source]

Differential effects of genotoxic stress on both concurrent body growth and gradual senescence in the adult zebrafish

AGING CELL, Issue 2 2007
Stephanie B. Tsai
Summary Among vertebrates, fish and mammals show intriguing differences in their growth control properties with age. The potential for unlimited or indeterminate growth in a variety of fish species has prompted many questions regarding the senescent phenomena that appear during the aging process in these animals. Using zebrafish as our model system, we have attempted in our current study to examine the growth phenomena in fish in relation to the onset of senescence-associated symptoms, and to evaluate the effects of genotoxic stress on these processes. We observed in the course of these analyses that the zebrafish undergoes continuous growth, irrespective of age, past the point of sexual maturation with gradually decreasing growth rates at later stages. Animal population density, current body size and chronological age also play predominant roles in regulating zebrafish growth and all inversely influence the growth rate. Interestingly, the induction of genotoxic stress by exposure to ionizing radiation (IR) did not adversely affect this body growth ability in zebrafish. However, IR was found to chronically debilitate the regeneration of amputated caudal fins and thereby induce high levels of abnormal fin regeneration in the adult zebrafish. In addition, by resembling and mimicking the natural course of aging, IR treatments likewise enhanced several other symptoms of senescence, such as a decline in reproductive abilities, increased senescence-associated ,-galactosidase activity and a reduction in melatonin secretion. Our current data thus suggest that during the lifespan of zebrafish, the onset of senescence-associated symptoms occurs in parallel with continuous growth throughout mid-adulthood. Moreover, our present findings indicate that genotoxic DNA damage may play a role as a rate-limiting factor during the induction of senescence, but not in the inhibition of continuous, density-dependent growth in adult zebrafish. [source]