The peri-saccadic perception of objects and space

Eye movements affect object localization and object recognition. Around saccade onset, briefly flashed stimuli appear compressed towards the saccade target, receptive fields dynamically change position, and the recognition of objects near the saccade target is improved. These effects have been attributed to different mechanisms. We provide a unifying account of peri-saccadic perception explaining all three phenomena by a quantitative computational approach simulating cortical cell responses on the population level. Contrary to the common view of spatial attention as a spotlight, our model suggests that oculomotor feedback alters the receptive field structure in multiple visual areas at an intermediate level of the cortical hierarchy to dynamically recruit cells for processing a relevant part of the visual field. The compression of visual space occurs at the expense of this locally enhanced processing capacity.     

An integrated approach to life-cycle evolution using selective landscapes

A model which defines fitness in terms of the intrinsic rate of increase of phenotypes is used to analyse which life cycles are appropriate to which ecological circumstances. The following predictions are made for asexual animals and those sexual animals producing on average more than one daughter per brood. If there are no behavioural or physiological interactions between variables, then number of offspring per breeding should be maximized, survival until first/next breeding should be maximized, and time to first/next breeding should be minimized. If interactions occur such that altering one life-cycle variable affects another, then there are trade-offs between variables and the optimum trade-off will maximize fitness.Number of offspring per breeding will generally affect adult survivorship until next breeding. Given certain reasonable assumptions about this trade-off, high juvenile survivorship selects towards semelparity (many offspring per brood), low juvenile survivorship selects towards iteroparity (few offspring per brood). If juvenile survival depends on adult feeding, as in altricial birds, then juvenile survivorship declines as clutch size is increased. Optimal clutch size maximizes the number of surviving offspring per brood.Two trade-offs involve parental care. If parents guard their offspring they should take more risks if brood size is larger. The amount that parents feed their offspring should depend on how effective feeding is in enhancing growth. Growth may also be enhanced by taking risks, in juveniles or adults. The extent of risk-taking should depend on how effective risk-taking is in enhancing growth.If the number of offspring per brood is related to growing conditions for offspring, the prediction is that more offspring per brood should be produced if growing conditions for offspring are better. If the adult can protect the offspring, for example by encapsulating them, the amount of protection provided should depend on how effective the protection is in increasing offspring survivorship.     

Energy allocation rules inDaphnia magna: clonal and age differences in the effects of food limitation

Summary The allocation of energy to carapace formation, respiration, growth, and reproduction were examined in two parthenogenetic clones ofDaphnia magna (Cladocera) cultured at two levels of food (Chlorella) concentration. Clonal differences in energy allocation were more apparent at high ration (1.5 g C mL^-1) than at low ration (0.3 g C mL^-1). These differences included respiratory and molting costs, and the timing of energy allocation to growth and reproduction. A comparison of active vs. anesthetized animals revealed that the interclonal difference in respiration rate was the result of a difference in activity level. In both clones mass-specific rates of respiration, growth, and brood production all decreased at low vs. high ration levels, whereas mass-specific molt-loss rate increased. Lowered food concentration decreased the relative allocation of energy to growth and reproduction, but increased allocation to maintenance (respiration and carapace formation). These allocation responses to food limitation indicated that for both clones the highest energy priority was carapace formation. However, the relative priority of respiration, growth and reproduction varied with age and clone. In juveniles (instars 1–4) the priority ranking of growth was essentially equal to that of respiration, whereas respiration always had higher priority in adults (instars 5–9). All three possibilities for the relative ranking of growth and reproduction (i.e., growth>reproduction, growth=reproduction, and reproduction>growth), as specified by different models in the literature, were observed depending on age and clone. The energy allocation rules were also shown to vary between other daphniid species. Furthermore, metabolic responses to chronic food limitation may be different from responses to acute food deprivation. In this study, one clone showed a greater decrease in respiration rate as a result of lifetime food limitation than did the other, but the opposite was true when these clones were exposed to 48 h of starvation. These differences in allocation rules and in acute vs. chronic responses may have to be considered when using physiological data to modelDaphnia populations.     

Comparative ecology of Gammarus pulex (L.) and Asellus aquaticus (L.) I: population dynamics and microdistribution

Gammarus pulex and Asellus aquaticus generally occupy different zones in rivers; the former occurs in upper reaches but is replaced by the latter in lower reaches. Microdistribution and life-history patterns of G. pulex and A. aquaticus in sympatry and allopatry, were analyzed. Both species exhibited similar patterns of microhabitat selection, with larger individuals associated predominantly with large-sized substratum particles, and juveniles with weed. Coexisting populations of G. pulex and A. aquaticus had similar densities and population dynamics. Within each species, differences in population dynamics of allopatric and sympatric populations were observed. Although variation in population dynamics of G. pulex may be explained in terms of competition between the two species, the evidence is weak and equivocal. Differences in the dynamics of the two A. aquaticus populations were possibly a consequence of coal-mine and organic pollution, reducing the survival of offspring in the allopatric population.     

Scope for growth in Gammarus pulex,a freshwater benthic detritivore

Although toxic substances affect the physiological processes of individual organisms, their ecological impacts occur at the population and community levels. However, physiological processes can often be assessed more easily and precisely than population and community ones. Here we argue that scope for growth, the difference between the energy input to an organism from its food and the output from respiratory metabolism, can give a good physiological measure of stress that, at least in principle, is straightforwardly related to population and community processes. We describe, in detail, how scope for growth can be measured in Gammarus pulex (Crustacea, Amphipoda). The results indicate that both zinc and low pH can significantly reduce the scope for growth of individuals and that the most sensitive component of the energy budget is food absorption.     

On the nature and possible utility of epilithic detritus

Epilithic detritus is recognized as a rich and potentially useful form of detrital material in aquatic habitats. It forms an adherent cover to the light-shaded, under-sides of submerged stones. Compared with other aquatic detrital materials it was found to be rich in organic material, protein and total potential energy content. It probably represents a primary seral stage in community succession which is prevented from maturing further by the absence of light. The potential usefulness of epilithic detritus, as food to aquatic detrivores, is discussed.     

Asexual reproduction in protozoa and invertebrates

A model which defines fitness in terms of rate of clone increase, and which assumes constant mortality, predicts that more smaller offspring should be produced in conditions which are good for individual growth. Evidence from the Protozoa, freshwater flatworms and anthozoan cnidarians support this prediction.Fitness is maximized by budding (or paratomous fission) if adult survivorship or growth is unaffected by offspring attachment to parent but time to first breeding is thereby reduced. Whether or not the adult is affected by offspring attachment is likely to depend on how mobile the adult is, so we assess the occurrence of offspring attachment in relation to adult mobility. It seems that budding is associated with a sessile life-style in the ciliated Protozoa, and usually in the cnidarians. Paratomy is associated with an interstitial existence in the mobile acoel and rhabdocoel turbellarians and the aeolosomatid and naidid annelids. Budding is rare in the solitary Anthozoa and the holothuroidean echinoderms, both of which are sessile. However in these animals survival of the adult is dependent on whole body contractions and would be impaired by the existence of buds.We predict what proportion of adult resources should be devoted to reproduction, and we consider the complication of encapsulation.     

Population growth rate as a basis for ecological risk assessment of toxic chemicals

Assessing the ecological risks of toxic chemicals is most often based on individual-level responses such as survival, reproduction or growth. Such an approach raises the following questions with regard to translating these measured effects into likely impacts on natural populations. (i) To what extent do individual-level variables underestimate or overestimate population-level responses? (ii) How do toxicant-caused changes in individual-level variables translate into changes in population dynamics for species with different life cycles? (iii) To what extent are these relationships complicated by population-density effects? These issues go to the heart of the ecological relevance of ecotoxicology and we have addressed them using the population growth rate as an integrating concept. Our analysis indicates that although the most sensitive individual-level variables are likely to be equally or more sensitive to increasing concentrations of toxic chemicals than population growth rate, they are difficult to identify a priori and, even if they could be identified, integrating impacts on key life-cycle variables via population growth rate analysis is nevertheless a more robust approach for assessing the ecological risks of chemicals. Populations living under density-dependent control may respond differently to toxic chemicals than exponentially growing populations, and greater care needs to be given to incorporating realistic density conditions (either experimentally or by simulation) into ecotoxicological test designs. It is impractical to expect full life-table studies, which record changes in survival, fecundity and development at defined intervals through the life cycle of organisms under specified conditions, for all relevant species, so we argue that population growth rate analysis should be used to provide guidance for a more pragmatic and ecologically sound approach to ecological risk assessment.