The interaction of temperature and fish size on growth of juvenile turbot

Growth rate of tagged juvenile turbot was significantly influenced by the interaction of temperature and fish size. The results suggest the optimum temperature for growth of juvenile turbot in the size range 25–75 g is between 16 and 19°C. Optimal temperature for growth decreased rapidly with increasing size, and is between 13 and 16°C for 100 g turbot. Although individual growth rates varied highly at all times within the temperature treatments, significant size rank correlations were maintained during the experimental period. The study confirms that turbot exhibit ontogenetic variation in temperature optimum, which might partly explain different spatial distribution of juvenile and adult turbot in ocean waters.     

Experimental and model analyses of the effects of competition on individual size variation in wood frog (Rana sylvatica) tadpoles

1. Size variation is a ubiquitous feature of animal populations and is predicted to strongly influence species abundance and dynamics; however, the factors that determine size variation are not well understood. 2. In a mesocosm experiment, we found that the relationship between mean and variation in wood frog (Rana sylvatica) tadpole size is qualitatively different at different levels of competition created by manipulating resource supply rates or tadpole density. At low competition, relative size variation (as measured by the coefficient of variation) decreased as a function of mean size, while at high competition, relative size variation increased. Therefore, increased competition magnified differences in individual performance as measured by growth rate. 3. A model was developed to estimate the contribution of size-dependent factors (i.e. based on size alone) and size-independent factors (i.e. resulting from persistent inherent phenotypic differences other than size that affect growth) on the empirical patterns. 4. Model analysis of the low competition treatment indicated that size-dependent factors alone can describe the relationship between mean size and size variation. To fit the data, the size scaling exponent that describes the dependence of growth rate on size was determined. The estimated value, 0-83, is in the range of that derived from physiological studies. 5. At high competition, the model analysis indicated that individual differences in foraging ability, either size-based or due to inherent phenotypic differences (size-independent factors), were much more pronounced than at low competition. The model was used to quantify the changes in size-dependent or size-independent factors that underlie the effect of competition on size-variation. In contrast to results at low competition, parameters derived from physiological studies could not be used to describe the observed relationships. 6. Our experimental and model results elucidate the role of size-dependent and size-independent factors in the development of size variation, and highlight and quantify the context dependence of individual (intrapopulation) differences in competitive abilities.     

Natal movement in juvenile Atlantic salmon: a body size-dependent strategy?

If competitive ability depends on body size, then the optimal natal movement from areas of high local population density can also be predicted to be size-dependent. Specifically, small, competitively-inferior individuals would be expected to benefit most from moving to areas of lower local density. Here we evaluate whether individual variation in natal movement following emergence from nests is consistent with such a size-dependent strategy in Atlantic salmon, and whether such a strategy is evident across a range of environmental conditions (principally predator presence and conspecific density). In stream channel experiments, those juveniles that stayed close to nests were larger than those that emigrated. This result was not sensitive to predator presence or conspecific density. These observations were mirrored in natural streams in which salmon eggs were planted in nests and the resulting offspring were sampled at high spatial resolution. A negative relationship was found between juvenile body size and distance from nests early in development whereas in those streams sampled later in ontogeny, individuals that had moved furthest were largest. Thus, movement away from nests appeared to result in a reduced competitive intensity and increased growth rate. The fact that there is ultimately a growth advantage associated with moving suggests that there is also a cost that selects against movement by the larger individuals. Thus, natal movement in juvenile Atlantic salmon appears to represent a body size-dependent strategy.     

Individual size variation and population stability in a seasonal environment: a discrete-time model and its calibration using grasshoppers

Much recent literature is concerned with how variation among individuals (e.g., variability in their traits and fates) translates into higher-level (i.e., population and community) dynamics. Although several theoretical frameworks have been devised to deal with the effects of individual variation on population dynamics, there are very few reports of empirically based estimates of the sign and magnitude of these effects. Here we describe an analytical model for size-dependent, seasonal life cycles and evaluate the effect of individual size variation on population dynamics and stability. We demonstrate that the effect of size variation on the population net reproductive rate varies in both magnitude and sign, depending on season length. We calibrate our model with field data on size- and density-dependent growth and survival of the generalist grasshopper Melanoplus femurrubrum. Under deterministic dynamics (fixed season length), size variation impairs population stability, given naturally occurring densities. However, in the stochastic case, where season length exhibits yearly fluctuations, size variation reduces the variance in population growth rates, thus enhancing stability. This occurs because the effect of size variation on net reproductive rate is dependent on season length. We discuss several limitations of the current model and outline possible routes for future model development.     

Size-dependent growth and the development of inequality in maize,sunflower and soybean

Links were investigated between allometry of plant growth and dynamics of size structure of well-fertilized, irrigated crops of soybean (Glycine max L.), sunflower (Helianthus annuus L.) and maize (Zea mays L.) grown at standard plant-population densities (D), as in commercial crops (D = 30, 6 and 8.5 plants m-2, respectively), and at high densities (2D). Patterns of size-dependent growth of shoot and seed mass accumulation were distinctly different among species. In soybean and sunflower, non-linear relationships between size and subsequent growth led to strong hierarchical populations in terms of both shoot and seed biomass. Curvilinear (soybean) and sigmoid (sunflower) size-dependent growth determined strongly asymmetrical (soybean) and bimodal (sunflower) frequency distributions of shoot biomass indicating predominantly size asymmetrical competition among individuals. In comparison, a lower plant-to-plant variation coupled with a typical linear allometry of growth to plant size indicated symmetrical two-sided plant interference in maize. Despite the weak development of hierarchies in shoot biomass, a strong inequality in reproductive output developed in crowded populations of maize indicating an apparent breakage of reproductive allometry.     

Shoot growth dynamics and size-dependent shoot fate of a clonal plant,Festuca rubra, in a mountain grassland

The relation of the within-season and between-season patterns of shoot growth were compared in a clonal grass with long-lived shoots,Festuca rubra, in a mown mountain grassland. The growth rate of shoot length from spring to summer in a year was almost constant for each shoot irrespective of spring shoot length each year. The annual shoot growth rate from spring to spring was negatively correlated with the shoot length in the first spring. Shoots of different length and age therefore tended to converge over time to a population of identical shoot size, suggesting an equalizing effect of growth pattern on size structure. Shoot size (shoot length and number of leaves) influenced the fates of shoots. Larger shoots showed an increased incidence of both flowering and formation of intravaginal daughter shoots and a decreased incidence of death in the subsequent time period. The fates of shoots were independent of their age. Although the negatively size-dependent springto-spring annual shoot growth rate acted to decrease shoot size variation, the remaining variation within the shoot population was still sufficient to generate different fates of shoots. These fates were not related to the previous life history of individual shoots. There was a significantly positive effect of the shoot size at initiation on its life expectancy. This was mainly attributable to the positively size-dependent survival rate of shoots in the early stage (<1 year old) of shoot life history. Later on (> 1 year old), shoot size had little effect on the survival rate of shoots. Once small young shoots have survived this early stage (< 1 year old) in life history, they can grow vigorously, little affected by competition regardless of shoot size, and converge to a stable size structure of shoots of similar size. Only shoot size in the early stage ( < 1 year old) of life history is important for the persistence of a shoot population.     

Regulation of growth in turbot (Scophthalmus maximus Rafinesque) and Atlantic halibut (Hippoglossus hippoglossus L.): aspects of environment × genotype interactions

This review is aimed atelucidating the mechanisms that regulate growthin cultured juvenile Atlantic halibut (Hippoglossus hippoglossus) and turbot (Scophthalmus maximus) by evaluating thesignificance of environmental factors(temperature, photoperiod) and the interactionsbetween them. In addition, we examine growthproperties in three populations of juvenilehalibut and turbot in order to elucidate anygeographical differences in growth and growthefficiency in these species. Both temperatureand photoperiod have a significant andpersistent effect on growth rate in bothspecies. Temperature tolerance, demonstrated bya wide temperature range supporting maximalgrowth, increased with size. Fish subjected tocontinuous light exhibited faster growth thanthose experiencing a natural photoperiod or aconstant short day. Moreover, when thephotoperiod increased naturally with day-lengthor when fish were abruptly switched from beingreared on short-day conditions to continuouslight, a subsequent increase in growth rate wasobserved. This growth enhancing effect ofextended photoperiods was more apparent in ashort time scale in Atlantic halibut than inturbot, but both species show significantlong-term effects of extended photoperiods.Enhanced growth in fish in continuous light waspartly explained by higher growth efficiency.In both species, there was a significantinteraction between temperature andphotoperiod, suggesting that thegrowth-enhancing effect of continuous light isrelatively stronger at lower temperatures.Growth rate in both species was alsosignificantly influenced by the interaction oftemperature and fish size, as the optimaltemperature for growth decreased rapidly withincreasing fish size. Differences in growth,food intake, food conversion efficiency,metabolism, ammonia excretion and RNA/DNAratios in white muscle were observed betweendifferent strains of halibut and turbot, withthe best growth properties being observed inthe northern populations. These findings onhalibut and turbot partly support the theory ofcountergradient variation in growth, suggestingthat populations from high latitudes havehigher growth capacity than populations fromlow latitudes.     

The influence of juvenile and adult environments on life-history trajectories

There is increasing evidence that the environment experienced early in life can strongly influence adult life histories. It is largely unknown, however, how past and present conditions influence suites of life-history traits regarding major life-history trade-offs. Especially in animals with indeterminate growth, we may expect that environmental conditions of juveniles and adults independently or interactively influence the life-history trade-off between growth and reproduction after maturation. Juvenile growth conditions may initiate a feedback loop determining adult allocation patterns, triggered by size-dependent mortality risk. I tested this possibility in a long-term growth experiment with mouthbrooding cichlids. Females were raised either on a high-food or low-food diet. After maturation half of them were switched to the opposite treatment, while the other half remained unchanged. Adult growth was determined by current resource availability, but key reproductive traits like reproductive rate and offspring size were only influenced by juvenile growth conditions, irrespective of the ration received as adults. Moreover, the allocation of resources to growth versus reproduction and to offspring number versus size were shaped by juvenile rather than adult ecology. These results indicate that early individual history must be considered when analysing causes of life-history variation in natural populations.     

Inequality of size and size increment in Pinus banksiana in relation to stand dynamics and annual growth rate

BACKGROUND AND AIMS: Changes in size inequality in tree populations are often attributed to changes in the mode of competition over time. The mode of competition may also fluctuate annually in response to variation in growing conditions. Factors causing growth rate to vary can also influence competition processes, and thus influence how size hierarchies develop. METHODS: Detailed data obtained by tree-ring reconstruction were used to study annual changes in size and size increment inequality in several even-aged, fire-origin jack pine (Pinus banksiana) stands in the boreal shield and boreal plains ecozones in Saskatchewan and Manitoba, Canada, by using the Gini and Lorenz asymmetry coefficients. KEY RESULTS: The inequality of size was related to variables reflecting long-term stand dynamics (e.g. stand density, mean tree size and average competition, as quantified using a distance-weighted absolute size index). The inequality of size increment was greater and more variable than the inequality of size. Inequality of size increment was significantly related to annual growth rate at the stand level, and was higher when growth rate was low. Inequality of size increment was usually due primarily to large numbers of trees with low growth rates, except during years with low growth rate when it was often due to small numbers of trees with high growth rates. The amount of competition to which individual trees were subject was not strongly related to the inequality of size increment. CONCLUSIONS: Differences in growth rate among trees during years of poor growth may form the basis for development of size hierarchies on which asymmetric competition can act. A complete understanding of the dynamics of these forests requires further evaluation of the way in which factors that influence variation in annual growth rate also affect the mode of competition and the development of size hierarchies.     

The effect of size-dependent growth and environmental factors on animal size variability

The origin of variation in animal growth rate and body size is not well understood but central to ecological and evolutionary processes. We develop a relationship that predicts the change in relative body size variation within a cohort will be approximately equal to the relative change in mean per unit size growth rate, when only size-dependent factors affect growth. When modeling cohort growth, relative size variation decreased, remained unchanged, or increased, as a function of growth rate-size scaling relationships, in a predictable manner. We use the approximation to predict how environmental factors (e.g., resource level) affect body size variation, and verified these predictions numerically for a flexible growth model using a wide range of parameter values. We also explore and discuss the assumptions underlying the approximation. We find that factors that similarly affect mean growth rate may differently affect size variation, and competition may increase body size variation without changing size-independent relationships. We discuss implications of our results to the choice of growth equations used in models where body size variation is an important variable or output.     

Effects of Group Membership and Size Distribution within a Group on Growth Rates of Juvenile Sablefish Anoplopoma fimbria

Group membership can confer both advantages and disadvantages to growth in juvenile fishes. The balance between costs and benefits of social interactions can shift depending on such factors as the composition of the group (density and size disparity) and the availability of food. We examined the effect of these factors on absolute growth and growth depensation in juvenile sablefish, Anoplopoma fimbria. Increasing density and increasing size disparity had little influence on absolute growth rates of juvenile sablefish and the effects of these social factors were not modified by ration level. In experiments testing density effects, absolute growth did not differ among groups of 1, 3, or 10 fish held at high rations, but at low rations single fish exhibited a different pattern of size-dependent growth compared to fish in groups. In experiments testing disparity effects, absolute growth did not differ between groups with an even size distribution and groups with a mixed size distribution. The relative size of an individual within a group, i.e., small, medium, or large, also did not modify growth, despite evidence of higher chasing behavior in mixed size distributions. Although the growth of small fish was not diminished in the presence of large fish, negative impacts of size disparity were expressed in high levels of cannibalism, which occurred in 42% of groups with a mixed size distribution. Significant growth depensation over time occurred in the density experiment, but not in the size disparity experiment, possibly due to the shorter duration of the latter experiment. We suggest that growth depensation was generated by individual variability in growth capacity rather than social effects on growth rates. Schooling behavior, measured by group cohesion indices, increased with fish size and was higher in groups with an even vs. a mixed size distribution. These results for sablefish are consistent with other schooling species in which growth variability is determined by exploitative competition and/or genetic variability in growth capacity rather than interference competition.     

The Roles of Spatial Pattern and Size Variation in Shaping Height Inequality of Plant Population

Game-theoretic models predict that there is an ESS height for the plant population to which all individual plants should converge. To attain this conclusion, the neighborhood factors were assumed to be equal for all the individual plants, and the spatial pattern and size variation of population were left without consideration, which is clearly not right for the scenario of plant competition. We constructed a spatially-explicit, individual-based model to explore the impacts of spatial structure and size variation on individual plant’s height and population’s height hierarchies under the light competition. The monomorphic equilibrium of height that all the individual plants will converge to only exists for a population growing in a strictly uniform spatial pattern with no size variation. When the spatial pattern of the population is non-uniform or there’s size variation among individual plants, the critical heights that individual plants will finally reach are different from each other, and the height inequality at the end of population growth will increase when the population’s spatial pattern’s degree of deviation from uniform and population’s size variation increase. Our results argue strongly for the importance of spatial pattern and neighborhood effects in generating the diversity of population’s height growth pattern.     

Simplifying a physiologically structured population model to a stage-structured biomass model

We formulate and analyze an archetypal consumer-resource model in terms of ordinary differential equations that consistently translates individual life history processes, in particular food-dependent growth in body size and stage-specific differences between juveniles and adults in resource use and mortality, to the population level. This stage-structured model is derived as an approximation to a physiologically structured population model, which accounts for a complete size-distribution of the consumer population and which is based on assumptions about the energy budget and size-dependent life history of individual consumers. The approximation ensures that under equilibrium conditions predictions of both models are completely identical. In addition we find that under non-equilibrium conditions the stage-structured model gives rise to dynamics that closely approximate the dynamics exhibited by the size-structured model, as long as adult consumers are superior foragers than juveniles with a higher mass-specific ingestion rate. When the mass-specific intake rate of juvenile consumers is higher, the size-structured model exhibits single-generation cycles, in which a single cohort of consumers dominates population dynamics throughout its life time and the population composition varies over time between a dominance by juveniles and adults, respectively. The stage-structured model does not capture these dynamics because it incorporates a distributed time delay between the birth and maturation of an individual organism in contrast to the size-structured model, in which maturation is a discrete event in individual life history. We investigate model dynamics with both semi-chemostat and logistic resource growth.     

Co-evolution of seed size and seed predation

Using the evolutionarily stable strategy (ESS) approach in a model for the co-evolution of seed size and seed predation, I show that seed size variation within individual plants is favoured if there is a trade-off in the predator's attack rate for different seed sizes. A single seed size is not evolutionarily stable because a predator that is optimally adapted to one particular seed size cannot prevent invasion by plants with a different seed size. The model generates the following predictions. The ESS consists of a continuous range of seed sizes. Small seeds tend to be attacked more frequently than big seeds. Plants with many resources and plants with low (frequency-independent) juvenile mortality have more variable seeds than plants with few resources and a high juvenile mortality. Seed size variation is higher in fluctuating populations regulated by seed predation alone than in stable populations (partially) regulated by seedling competition. Predator searching behaviour does not directly affect the ESS seed size range, but may have an indirect effect by affecting population stability or the significance of seedling competition as a population regulating mechanism. Moreover, seed size distributions are found to be more skewed in favour of small seeds if predation is spatially non-uniform than if predation is more even. Application of the model to systems of several co-evolving plant and predator species is discussed.     

Size-dependent sex change can be the ESS without any size advantage of reproduction when mortality is size-dependent

Almost all models of sex change evolution assume that reproductive rate increases with body size. However, size-dependent sex changing plants often show size-independent reproductive success, presumably due to pollen limitation. Can the observed size-dependent sex change pattern be the ESS in this case? To answer this question, we analyze a game model of size-dependent sex expression in plants. We assume: (1) reproductive rate is perfectly independent of size; (2) mortality decreases with size in the same way for both sexes; (3) growth rates decrease at maturity, more for females than males. We show that the ESS is size-dependent sex expression: small individuals are vegetative, intermediate individuals are male, and large individuals are female. These results demonstrate that mortality is important in size-dependent sex allocation even when mortality rate is independent of sex. They also offer an explanation of why we see populations in poor environments to have sex ratios more biased toward the first sex relative to high quality environments.     

Otolith accretion rates: Does size really matter?

This study examined the relationship between otolith size and growth in juvenile cod (Gadus morhua L.). Two groups of juvenile cod were reared under different food ration and temperature regimes to obtain fish of similar somatic size but with different sized otoliths. The two groups were subjected to alternating temperature regimes and intermediate ration levels. Large otoliths grew significantly faster than the small ones and variation between individuals was extensive. The ratio of otolith growth during cold and warm temperature exposure did not differ between groups, and the observed growth pattern is therefore not attributable to differential growth within individual temperature periods. The ratio decreased with otolith size, presumably as a result of ontogenetic decrease in otolith protein composition. These results suggest that processes coupled to the metabolic rate of the endolymphatic epithelium are the key driver behind otolith growth.     

The physiology of rainbow trout in social hierarchies: two ways of looking at the same data

Salmonids form dominance hierarchies in environments, where space or food are limiting. Our first objective was to investigate the physiology of individual rainbow trout in 4-fish hierarchies. Our second was to compare conclusions drawn from grouping physiological data on the basis of social rank with those based on relating individual physiology to individual aggressive behavior. To create a social hierarchy, groups of 4 juvenile trout were fed (1 % ration) using a darkened feeding container, twice daily (morning and evening). Each morning feeding was videotaped to record aggressive behavior, thereby facilitating the assignment of a social status rank to each fish. On days 5 and 10–11, physiological parameters were measured in fish fasted for 24 h. Social hierarchies formed in all tested groups. One fish would become dominant, whereas the three subordinate individuals would each assume a stable social rank. When classified according to this social rank, the three subordinate individuals all displayed similar physiology, different from the physiology of the dominant fish. The latter included higher ammonia excretion rate, greater protein utilization in aerobic metabolism, greater feeding, higher specific growth rate, greater increase in condition factor, and lower routine oxygen consumption rate. However, when individual aggression was taken into account, a continuous gradient was observed between aggression and physiology for most parameters, regardless of social status. These relationships could be improved by normalizing the aggression score to the overall level of aggression in each hierarchy. We argue that individual behavior should be considered instead of just social rank when studying the physiology of trout in social hierarchies.     

A model for the dynamics of an annual plant population

A model for the dynamics of a single species population of plants is proposed and its use demonstrated by the analysis of a simple example. The model incorporates the effects of microsite variation by allowing for individual differences in growth and death rates within each season. We demonstrate that an increase in the variance in individual growth rates may increase both the chances that a plant population will persist and the equilibrium size of that population. We also show that even if size-dependent death is occurring, it may not have a significant effect on the shape of the size frequency distribution. An extension of the model to multispecies communities of plants suggests an experimental procedure to determine whether competition is responsible for excluding a particular plant species from a community that appears otherwise to be suitable. A more detailed analysis of the model for a two-species community produces conditions for competitive coexistence reminiscent of those from the Lotka-Volterra competition equations. Another extension suggests that selection will favor those genotypes that maximize the product of germination probability and mass of seeds produced, if survivorship and growth are not substantially altered. Finally, an analog to r- and K-selection theory for animal populations is developed. Selection in low-density populations favors increasing growth rate, and in high-density populations favors minimizing the effect of neighbors on one's own growth rate.     

Size and growth relationships in juvenile steelhead: The advantage of large relative size diminishes with increasing water temperatures

In territorial stream salmonids, asymmetric competition can perpetuate individual size differences over time, but the extent to which this is manifested can be environmentally mediated. Here we study the variation in juvenile steelhead (Oncorhynchus mykiss) growth rates to identify the conditions (population density and water temperature) under which an individual’s size relative to its conspecifics conferred an advantage. Among steelhead rearing in the same stream section we found that relatively larger individuals on average grew faster than smaller conspecifics. However, comparing across stream sections there was a negative interaction between relative size and water temperature. The effect of an individual’s relative size on its growth rate decreased as temperatures were increasing, indicating that the advantages of being large diminished during periods of high temperatures or in locations with relatively higher temperatures. Compared to temperature, the effects of population density on the growth rate were less substantial. The results suggest that larger individuals on average acquire more resources than smaller individuals, and demonstrate that water temperature exerts an important, modulating control over growth performance in heterogeneous environments.     

青藏高原不同生境下湿生扁蕾(Gentianopsis paludosa)个体大小依赖的繁殖分配

植物对资源的投资和分配是生态学中的重要问题,它反映了植物应对环境变化时的生活史策略。选择青藏高原东缘同一海拔下的嵩草草甸(Kobresia sp.meadow)、金露梅灌丛(Potentilla fruticosa shrub meadow)以及草甸-灌丛交错带3种生境类型,并以3种生境下的湿生扁蕾(Gentianopsis paludosa)为对象,研究了其繁殖分配特征。结果发现:(1)在种群水平上,在生境从草甸经交错带到灌丛的变化中,湿生扁蕾个体大小和繁殖分配比例逐渐增加;3个种群湿生扁蕾的总花数目没有显著差异,但草甸生境湿生扁蕾的蕾期花数目显著高于灌丛生境,而果期花数目则显著低于灌丛生境;(2)在个体水平上,湿生扁蕾的繁殖绝对投入与个体大小显著正相关,且各种群植株都存在繁殖所需的个体大小阈值,而繁殖阈值在生境从草甸经交错带到灌丛的过渡中逐渐减小;湿生扁蕾的繁殖相对投入与个体大小负相关,但相关系数随着生境从草甸经交错带到灌丛的过渡中逐渐减小;各种群花数目与湿生扁蕾植株个体大小显著正相关。研究表明,湿生扁蕾的繁殖投资存在大小依赖效应,但生境差异会对其繁殖投资和生活史策略造成显著影响,而这种影响主要是由不同生境下自然条件的不同造成的。同时,资源分配也与湿生扁蕾的遗传特性和延迟自交的繁育系统特征有关。湿生扁蕾这种不同生境下个体大小依赖的繁殖投资差异是湿生扁蕾与其生境长期适应和进化(生境选择)的结果。