Atlantic salmon growth in strongly food-limited environments: Effects of egg size and paternal phenotype?

I manipulated egg size and followed individual mass trajectories from the egg stage in Atlantic salmon to test for effects of size, and for interactions between size and paternal body mass, on offspring performance in strongly food-limited environments. Egg size had a strong effect on body mass at yolk absorption, causing juveniles originating from large eggs to outgrow their siblings from small eggs. This corroborates previous findings of egg size effects under more benign environments, and demonstrates that positive effects of egg size on offspring success are manifested even under strong food-limitation. Previously reported negative effects of being large during the critical period for survival in dense populations are thus likely related to social interactions, rather than to effects of density on total food abundance in the environment. The effect of egg size on offspring performance, and hence the optimal egg size, was independent of paternal body mass.     

Life-history consequences of egg size in Drosophila melanogaster

We used a novel approach to study the effects of egg size on offspring fitness components in Drosophila melanogaster. Populations that differed genetically in egg size were crossed, and the female offspring from these reciprocal crosses were examined for life-history traits. These flies expressed effects of egg size, because they developed from eggs of different sizes as a result of maternal genetic effects, but displayed an equivalent range of nuclear genetic variation. The crosses used four independent pairs of outbred populations that differed in the pattern of covariation between egg size and life-history traits, so that the maternal genetic effects of egg size on offspring characters could be contrasted to the associations present among the parental populations. Egg size showed positive maternal genetic effects on embryonic viability and development rate, hatchling weight and feeding rate, and egg-larva and egg-adult development rate but no consistent effects on larval competitive ability, adult weight, or egg size in the offspring. Our method revealed a pattern of causality that could not be deduced from interpopulation comparisons and therefore provides a good way of disentangling the causes and consequences of variation in egg size while controlling for zygotic genetic effects.     

Bigger mothers are better mothers: disentangling size-related prenatal and postnatal maternal effects

Despite a vast literature on the factors controlling adult size, few studies have investigated how maternal size affects offspring size independent of direct genetic effects, thereby separating prenatal from postnatal influences. I used a novel experimental design that combined a cross-fostering approach with phenotypic manipulation of maternal body size that allowed me to disentangle prenatal and postnatal maternal effects. Using the burying beetle Nicrophorus vespilloides as model organism, I found that a mother''s body size affected egg size as well as the quality of postnatal maternal care, with larger mothers producing larger eggs and raising larger offspring than smaller females. However, with respect to the relative importance of prenatal and postnatal maternal effects on offspring growth, only the postnatal effects were important in determining offspring body size. Thus, prenatal effects can be offset by the quality of postnatal maternal care. This finding has implications for the coevolution of prenatal and postnatal maternal effects as they arise as a consequence of maternal body size. In general, my study provides evidence that there can be transgenerational phenotypic plasticity, with maternal size determining offspring size leading to a resemblance between mothers and their offspring above and beyond any direct genetic effects.     

Context-dependent intergenerational effects: the interaction between past and present environments and its effect on population dynamics

Intergenerational effects arise when parents' actions influence the reproduction and survival of their offspring and possibly later descendants. Models suggest that intergenerational effects have important implications for both population dynamical patterns and the evolution of life-history traits. However, these will depend on the nature and duration of intergenerational effects. Here we show that manipulating parental food environments of soil mites produced intergenerational effects that were still detectable in the life histories of descendents three generations later. Intergenerational effects varied in different environments and from one generation to the next. In low-food environments, variation in egg size altered a trade-off between age and size at maturity and had little effect on the size of eggs produced in subsequent generations. Consequently, intergenerational effects decreased over time. In contrast, in high-food environments, variation in egg size predominantly influenced a trade-off between fecundity and adult survival and generated increasing variation in egg size. As a result, the persistence and significance of intergenerational effects varied between high- and low-food environments. Context-dependent intergenerational effects can therefore have complex but important effects on population dynamics.     

Phylogenetic analyses of dimorphism in primates: evidence for stronger selection on canine size than on body size

Phylogenetic comparative methods were used to analyze the consequences of sexual selection on canine size and canine size dimorphism in primates. Our analyses of previously published body mass and canine size data revealed that the degree of sexual selection is correlated with canine size dimorphism, as well as with canine size in both sexes, in haplorhine but not in strepsirrhine primates. Consistent with these results, male and female canine size was found to be highly correlated in all primates. Since canine dimorphism and canine size in both sexes in haplorhines were found to be not only related to mating system but also to body size and body size dimorphism (characters which are also subject to or the result of sexual selection), it was not apparent whether the degree of canine dimorphism is the result of sexual selection on canine size itself, or whether canine dimorphism is instead a consequence of selection on body size, or vice versa. To distinguish among these possibilities, we conducted matched-pairs analyses on canine size after correcting for the effects of body size. These tests revealed significant effects of sexual selection on relative canine size, indicating that canine size is more important in haplorhine male-male competition than body size. Further analyses showed, however, that it was not possible to detect any evolutionary lag between canine size and body size, or between canine size dimorphism and body size dimorphism. Additional support for the notion of special selection on canine size consisted of allometric relationships in haplorhines between canine size and canine size dimorphism in males, as well as between canine size dimorphism and body size dimorphism. In conclusion, these analyses revealed that the effects of sexual selection on canine size are stronger than those on body size, perhaps indicating that canines are more important than body size in haplorhine male-male competition.     

Reduced fecundity in small populations of the rare plant Gentianopsis ciliate (Gentianaceae)

Habitat destruction is the main cause for the biodiversity crisis. Surviving populations are often fragmented, i.e., small and isolated from each other. Reproduction of plants in small populations is often reduced, and this has been attributed to inbreeding depression, reduced attractiveness for pollinators, and reduced habitat quality in small populations. Here we present data on the effects of fragmentation on the rare, self-compatible perennial herb Gentianopsis ciliata (Gentianaceae), a species with very small and presumably well-dispersed seeds. We studied the relationship between population size, plant size, and the number of flowers produced in 63 populations from 1996-1998. In one of the years, leaf and flower size and the number of seeds produced per fruit was studied in a subset of 25 populations. Plant size, flower size, and the number of seeds per fruit and per plant increased with population size, whereas leaf length and the number of flowers per plant did not. The effects of population size on reproduction and on flower size remained significant if the effects were adjusted for differences in plant size, indicating that they could not be explained by differences in habitat quality. The strongly reduced reproduction in small populations may be due to pollination limitation, while the reduced flower size could indicate genetic effects.     

Dispersal of the estuarine gastropod Pyrazus ebeninus is only weakly influenced by pneumatophore density

Studies on rocky intertidal gastropods indicate habitat complexity and body size to be major determinants of dispersal patterns. Considerations of effects of habitat complexity and body size on soft sediment gastropods are, however, less common. In neither habitat has the interaction between habitat complexity and body size been considered despite the increasing recognition in the general ecological literature that complexity effects are body-size-dependent. We tested independent and interacting effects of habitat complexity and body size on movement of the mud-whelk, Pyrazus ebeninus, by marking large (61-85 mm) and small (31-55 mm) snails in sites with low and high densities of pneumatophores and determining the distance and direction of their dispersal over periods of 1 week, 2 weeks and 1 month. Contrary to our expectation, we found no effect of pneumatophore density on the distance of snail migration over each of the temporal scales; net distance travelled by snails was determined only by body size and idiosynchratic, site-specific factors. The direction of snail movement was, by contrast, influenced on some temporal scales by both pneumatophore density and snail size. Over 1 week, site effects dominated patterns of movement and neither size of snail nor density of pneumatophore produced statistically significant effects. As the temporal scale increased, effects of size and pneumatophore density became increasingly apparent. Over the 1-month period, large snails at all sites and small snails at sites with high pneumatophore density migrated down the shore, while small snails at sites with low pneumatophore displayed non-directional movement. Thus, overall this study provides only weak support for effects of pneumatophore density on snail movement. In combination with other studies, our results suggest that, in comparison to on rocky shores where habitat complexity has strong effects on the distribution, abundance and behaviour of gastropods in soft-sediment systems habitat complexity is a less important structuring agent.     

The cost of reproduction induced by body size at birth and breeding density

Body size at birth has implications for the quality of individuals throughout their life. Although large body size is generally considered an advantage, the relationship between body size at birth and long-term fitness is often complicated. Under spatial or temporal variation in environmental conditions, such as the seasonally changing densities of Fennoscandian vole populations, selection should favor variation in offspring phenotypes, as different qualities may be beneficial in different conditions. We performed an experiment in which a novel hormonal manipulation method was used to increase phenotypic variance in body size at birth in the bank vole (Myodes glareolus). The effects of body size on the future fitness of young males and females were then studied at varying population densities in outdoor enclosures. Our results show that small body size at birth and high breeding density increase the survival costs of reproduction. However, there was no interaction between the effects of body size and density on survival, which suggests that the fitness effects of body size were strong enough to persist under environmental variation. Moreover, litter size and the probability of breeding were more sensitive to variation in breeding density than offspring size. Therefore, it is unlikely that individual fitness could be optimized by adjusting offspring body size to the prevailing population density through adaptive maternal effects. Our results highlight the significance of the costs of reproduction in the evolution of life-history traits, and give strong experimental support for the long-term fitness effects of body size at birth.     

Maternal effects on offspring size and number in mosquitofish,Gambusia holbrooki

Given a trade-off between offspring size and number, all mothers are predicted to produce the same optimal-sized offspring in a given environment. In many species, however, larger and/or older mothers produce bigger offspring. There are several hypotheses to explain this but they lack strong empirical support. In organisms with indeterminate growth, there is the additional problem that maternal size and age are positively correlated, so what are their relative roles in determining offspring size? To investigate this, we measured the natural relationship between maternal and offspring size in a wild population of Gambusia holbrooki (eastern mosquitofish), and experimentally disentangled the effects of maternal age and size on offspring size in the laboratory. In combination, our data indicate that the relationship between maternal and offspring size is nonlinear. Small mothers seem to produce larger than average offspring due to integer effects associated with very small broods. For extremely large mothers, which were only sampled in our wild data, these larger than average offspring may result from greater maternal resources or age effects. However, maternal age had no effect on offspring size or number in the laboratory experiment. Our results highlight the importance of sampling the full size–range of mothers when investigating maternal effects on offspring size. They also point to the difficulty of experimentally manipulating maternal size, because any change in size is invariably associated with a change in at least one factor affecting growth (be it temperature, food availability, or density) that might also have an indirect effect on offspring size.     

Maternal and paternal contributions to egg size and egg number variation in the blackfin pearl killifish <Emphasis Type="Italic">Austrolebias nigripinnis</Emphasis>

Reproductive effort, egg number and egg size are traditionally considered to be ‘female’ life history traits. However, females often adjust the amount of resources allocated to reproduction depending on their mate, causing male environmental effects on life history traits. If females respond to male traits which are genetically variable, then male environmental effects contain indirect genetic effects. Estimates of how much of the total variation in life history traits originates from female effects versus male environmental effects, seems mostly lacking. We have investigated variation in rates of egg production and in egg size in the annual Argentinian blackfin pearl killifish Austrolebias nigripinnis, in a crossed design where males were exchanged repeatedly between females. Our analysis of phenotypic variance components of reproductive effort, egg size and egg number indicates that the amount of variation contributed by male environmental effects is equal (egg size, reproductive effort) or larger (egg number) than that between females. For egg size and number, we find that male environmental effects consist of a male random effect representing the average response of females to male phenotype, plus a female-male interaction term. This term can be understood as the deviation from the population mean of an individual female’s response. For reproductive effort, we find that the male environmental effect consists of an interaction term only. Random effects on egg size and number additionally vary in magnitude depending on the weekday where we collected eggs, probably due to cyclic variation in experimental conditions. Since we find that both male phenotype and environmental conditions affect egg size and number as determined by females, our results suggest that selection on these life history traits will be frequency-dependent.     

The paradox of seed size and adaptation

Correlations between habitat and seed size suggest that this character is adaptive. Mean seed size is a relatively invariant species characteristic and seed size has marked effects upon fitness. These observations have previously led to the conclusion that seed size is under stabilizing selection. This conclusion, originally based mainly on evidence from crop plants grown in controlled environments, is questioned here on the grounds that recent studies of wild plants show marked phenotypic plasticity and low heritability of seed size. If seed size is not readily altered by natural selection in the wild, then its effects on fitness are evidence that this character is a constraint on habitat distribution. Constancy of mean seed size may be due to developmental canalization to a size set by previous selection, rather than a continuing process of stabilizing selection.     

On how risk and group size interact to influence vigilance

Vigilance allows animals to monitor their surroundings for signs of danger associated with predators or rivals. As vigilance is costly, models predict that it should increase when the risk posed by predators or rivals increases. In addition, vigilance is expected to decrease in larger groups that provide more safety against predators. Risk and group size are thus two key determinants of vigilance. Together, they could have additive or interactive effects. If risk and group size interacted, the magnitude of the group‐size effect on vigilance would vary depending on the level of risk experienced, implying that the benefits of sociality in terms of vigilance vary with risk. Depending on the model, vigilance is predicted to decrease more rapidly with group size at low risk or at high risk. Little work has focused directly on the interaction between risk and group size, making it difficult to understand under which conditions particular interactive effects arise and whether interactive effects are common in natural systems. I review the vast literature on vigilance in birds and mammals to assess whether interactive effects between risk and group size are common, and if present, which pattern occurs more frequently. In studies involving predation risk, the greatest proportion reported no statistically significant interactive effects. In other cases, vigilance decreased with group size more rapidly at low or high risk in a similar proportion of studies. In studies involving risk posed by rivals (social risk), most documented a more rapid decrease in vigilance with group size at low than at high risk, as predicted if the need to monitor rivals increases in larger groups. Low statistical power to detect interactive effects might have been an issue in several studies. The absence of interactive effects, on the other hand, might suggest constraints or limits on the ability of animals to adjust vigilance to current risk or group sizes. Interactive effects on vigilance have implications for the evolution of sociality and for our understanding of the phenotypic plasticity of predator‐ and competitor‐induced defences and deserve more attention in future studies.     

Factors affecting gastric evacuation in cod, Gadus morhua L., fed single-meals of natural prey

Functional relationships were derived in order to describe the effects of fish weight (262–2066 g), temperature (1–14° C), prey size and ration size (0.4–8.4% body weight) on gastric evacuation in cod fed four natural prey types. Interindividual (unexplained) differences among voluntary fed cod were relatively large. Power functions were appropriate for describing the effects of fish weight and ration size on the half-time of evacuation. Effects of meal and/or prey size appeared to counterbalance the effects of cod size. It is suggested that when cod of different sizes are fed fixed proportions of their body weight evacuation time is constant and independent of body size. There was found to be an exponential relationship between temperature and gastric evacuation time but, observations made at similar temperatures at different times of the year suggested that seasonal effects were of minor importance.     

Natural selection on body size is mediated by multiple interacting factors: a comparison of beetle populations varying naturally and experimentally in body size

Body size varies considerably among species and among populations within species, exhibiting many repeatable patterns. However, which sources of selection generate geographic patterns, and which components of fitness mediate evolution of body size, are not well understood. For many animals, resource quality and intraspecific competition may mediate selection on body size producing large-scale geographic patterns. In two sequential experiments, we examine how variation in larval competition and resource quality (seed size) affects the fitness consequences of variation in body size in a scramble-competing seed-feeding beetle, Stator limbatus. Specifically, we compared fitness components among three natural populations of S. limbatus that vary in body size, and then among three lineages of beetles derived from a single base population artificially selected to vary in size, all reared on three sizes of seeds at variable larval density. The effects of larval competition and seed size on larval survival and development time were similar for larger versus smaller beetles. However, larger-bodied beetles suffered a greater reduction in adult body mass with decreasing seed size and increasing larval density; the relative advantage of being large decreased with decreasing seed size and increasing larval density. There were highly significant interactions between the effects of seed size and larval density on body size, and a significant three-way interaction (population-by-density-by-seed size), indicating that environmental effects on the fitness consequences of being large are nonadditive. Our study demonstrates how multiple ecological variables (resource availability and resource competition) interact to affect organismal fitness components, and that such interactions can mediate natural selection on body size. Studying individual factors influencing selection on body size may lead to misleading results given the potential for nonlinear interactions among selective agents.     

Microbiota, fauna, and mesh size interactions in litter decomposition

Plant litter decomposition is a key process in carbon and nutrient cycling. The critical role of soil-faunal community composition in decomposition has been demonstrated using different mesh size litterbags to control exposure of litter to different faunal size classes. However, the faunal community surrounding the litterbags has not been manipulated despite potentially large indirect effects of their activity on biotic and abiotic processes that control litter decomposition at the habitat-scale.
We combined microcosm and litterbag techniques to facilitate a more comprehensive understanding of the role of direct and indirect effects of soil-faunal community composition on litter decomposition. We placed litterbags of three mesh sizes across model grassland miniecosystems manipulated to enable communities containing 1) microfauna; 2) micro- and meso-fauna; 3) micro-, meso- and macro-fauna. All communities contained bacteria and fungi. The approach permitted correction of mesh size artefacts inherent to field studies. Indirect effects have been divided into two separate terms, direct-indirect effects and indirect effects.
Decomposition in micromesh litterbags was significantly decreased by the indirect effects of meso- and macro-fauna. In macrofauna communities, increased mesh size significantly increased decomposition through mesh size per se and faunal effects. Relative effects of manipulated faunal community composition on litter mass loss and C:N ratio were equivalent for green and senesced litter. The presence of meso- and macro-fauna increased litter decomposition rate overall despite inhibiting decomposition by microfauna, bacteria and fungi through indirect effects.     

根田鼠瞬时摄入率对植物可利用性变量集功能反应的格局

在实验室条件下,以随机区组设计的新鲜紫花苜蓿叶片斑块,测定苜蓿叶片可利用性变量,叶片密度,生物量密度和叶片大小对根田鼠瞬时摄入率的作用格局。苜蓿叶片大小对根田鼠摄入率具有显作用（P＜0．01）,而叶片密度与生物量作用则不显（P＞0．05）;根田鼠摄入率对其口量变化能作出2倍以上的反应（P＜0．01）;观测摄入率与模型预测摄入率的回归显（P＜0．01）,研究结果证明,以叶片大小替代根田鼠口量是影响其摄率的独立变量;检验了植物大小是替代植食性哺乳动物口量的有效变量,以及植物大小是影响植食性哺乳动物摄入率潜在独立变量的假设。     

Size Effects on Mating and Egg Production in the Miami Blue Butterfly

Body size is often related to reproductive success in insects, but the direction and strength of this relationship differs greatly among systems. We studied the effects of adult size on probability of mating and egg production in the Miami blue butterfly. We found that likelihood of mating was invariant with respect to size. Larger females lived longer, and both size and lifespan positively influenced egg production. However, neither the number of copulations nor the size of male mates had any effect on female fecundity. We discuss these results in the context of butterfly mating systems, larval growth strategies and the possible effects of captive conditions on reproductive behavior.     

A global analysis of the determinants of alien geographical range size in birds

Aim Determining the causes of range size variation in the distributions of alien species is important for understanding the spread of invasive species. Factors influencing alien range size have been explored for some species at a regional level, but to date there has been no global analysis of an entire class. Here, we present such an analysis for birds, testing for the effects of introduction event, location and species‐level variables on alien range sizes. Location Global. Methods We used a novel dataset on the global distributions of alien bird species to test for relationships between alien range size and colonization pressure, residence time, extent of the global climatic niche, native range size, body mass and specialization, using a statistical approach based on phylogenetic generalized least squares models. We performed this analysis globally, and for separate biogeographical realms. Results Approximately half of the variation in alien bird range size is explained by colonization pressure in univariate analysis. We identified consistent effects of higher colonization pressure at global and realm levels, as well as support for effects of native range size and residence time. We found less support for effects of body mass, specialization or extent of the global climatic niche on alien range size. Main conclusions Alien bird range sizes are generally small relative to their native range sizes, and many are continuing to expand. Nevertheless, current variation is predictable, most strongly by the event‐level factor of colonization pressure. Whether a species is widespread is a better predictor of alien range size than whether a species could be widespread (estimated by global climatic niche extent), while we also find effects of residence time on alien range size. These relationships may help to identify those alien species that are more likely to spread and hence have greater environmental and economic impacts where they have been introduced.     

Parental environmental effects and cyclical dynamics in plant populations

Abstract Parental environmental effects have been widely reported in plants, but these effects are often weak relative to direct effects of current environmental conditions. Few studies have asked when consideration of such effects is necessary to understand long-term plant population dynamics. In this article, I show that inclusion of effects of parental density on offspring mass fundamentally changes population dynamics models by making recruitment a function of population size in two previous generations ([Formula: see text]), rather than one ([Formula: see text]). Models without parental density effects predict either stable population dynamics or sharp crashes from high to low population size (flip bifurcations). When parental effects are at least one-third the size of direct density effects, gradual cycles from high to low population size (Hopf bifurcations) are possible. In this study, I measured effects of parental and offspring density on offspring quality in an annual plant, Cardamine pensylvanica, by manipulating plant density independently in parent and offspring generations and by comparing the effects of parent and offspring density on offspring performance. Parental density effects were detectable but were noticeably weaker than offspring density effects. Nonetheless, the parental effect was large enough to change population dynamics predictions. Thus, parental effects may be an important component of the numerical dynamics of plant populations.     

Density dependence constrains mean growth rate while enhancing individual size variation in stream salmonids

The objective of this study was to elucidate the effects of density dependence on the individual size variation of brown trout (Salmo trutta) juveniles. Recruitment (the abundance of the youngest juveniles in May when they were 2 months old); the mean size attained by those individuals in September (6 months old) and the corresponding size variability around the mean size quantified with the coefficient of variation (CV) were examined in 22 year-classes at seven sites of two contrasting tributaries of the Rio Esva drainage (north-western Spain). Both mean size and CV tended to be site-specific but density dependence in the form of recruitment dependence affected both mean size and CV: the mean size depicted negative power relationships with increased recruitment whereas the CV increased positively with increased recruitment. However, this pattern differed among sites. At two out of seven sites, there was no obvious relationship between the mean size and recruitment. The CV increased positively with increased recruitment at all sites, although at several sites the CV described linear relationships and at others described power relationships. As a consequence, the stronger effects of density dependence on mean size occurred at low densities with minor effects at high densities, whereas density dependence operated on CV with continuous effects within the whole range of recruitment variation except at several sites where lower effects occurred at high densities. Thus, the occurrence, shape and intensity of competitive interactions underlying density dependence as a major cause of size variation differed across temporal and spatial scales.