Migration speeds and orientation of Atlantic salmon and sea trout post-smolts in a Norwegian fjord system

We recorded the observed and actual swimming speeds of Atlantic salmon and sea trout post-smolts in a Norwegian fjord system, and initiated studies on the orientation mechanisms of the post-smolts. We tracked Atlantic salmon and sea trout with acoustic transmitters for up to 14 h after release. The actual swimming speed and direction of a fish relative to the ground is the vector sum of the observed movements of the fish and the movements of the water. We determined actual swimming speeds and directions of the post-smolts, which reflect their real swimming capacities and orientation, by corrections for the speed and direction of the water current. The post-smolts were actively swimming. The observed direction of movement was dependent on the actual movement of the fish and not the water current. Water currents were not systematically used as an orientation cue either in Atlantic salmon or sea trout, as the actual movements were random compared to the direction of the water current. The actual movement of sea trout were in all compass directions, with no systematic pattern. The Atlantic salmon also moved in all compass directions, but with the lowest frequency of actual movement towards the fjord.     

Feeding activity of Callinectes ornatus Ordway, 1863 and Callinectes danae Smith, 1869 (Crustacea, Brachyura, Portunidae) in Ubatuba, SP, Brazil

The feeding activity along the day cycle and the time consumed for extracellular digestion were evaluated in the portunids C. ornatus and C. danae. Swimming crabs were obtained from trawling in Ubatuba bay, São Paulo, Brazil, during both the rainy and dry seasons. In each season, daily scheduled samples were taken at dawn (±6 h), noon (±12 h), dusk (±18 h) and midnight (±24 h). All individuals were dissected and the degree of stomach replenishment was recorded. In order to estimate the time elapsed for extracellular digestion, crabs were fed, and groups were dissected at 30 min intervals to check the conditions of their stomachs. In general, both species show a higher feeding activity during periods of lower light intensity, as evidenced by an increased percentage of full stomachs in dusk and midnight samples. The obtained results support higher feeding activity at night in these species and indicate short time for extracellular digestion, not exceeding 8 h. Nevertheless, full stomachs were recorded in all sampling schedules. In this case, it should be considered that elimination of certain food items such as fish bones, mollusk shells and carapace fragments of crustaceans could take more time than other items. Additionally, some crab species could require a cycle of cell replacement in the midgut gland epithelium until they can take their next meal.     

Effects of temperature on larval fish swimming performance: the importance of physics to physiology

Temperature influences both the physiology offish larvae and the physics of the flow conditions under which they swim. For small larvae in low Reynolds number (Re) hydrodynamic environments dominated by frictional drag, temperature‐induced changes in the physics of water flow have the greatest effect on swimming performance. For larger larvae, in higher Re environments, temperature‐induced changes in physiology become more important as larvae swim faster and changes in swimming patterns and mechanics occur. Physiological rates at different temperatures have been quantified using Q₁₀s with the assumption that temperature only affected physiological variables. Consequently, Q₁₀s that did not consider temperature‐induced changes in viscosity overestimated the effect of temperature on physiology by 58% and 56% in cold‐water herring and cod larvae respectively. In contrast, in warm‐water Danube bleak larvae, Q₁₀s overestimated temperature‐induced effects on physiology by only 5–7%. This may be because in warm water, temperature‐induced changes affect viscosity to a smaller degree than in cold water. Temperature also affects muscle contractility and efficiency and at high swimming velocities, efficiency decreases more rapidly in cold‐exposed than in warm‐exposed muscle fibres. Further experiments are needed to determine whether temperature acts differently on swimming metabolism in different thermal environments. While hydrodynamic factors appear to be very important to larval fish swimming performance in cold water, they appear to lose importance in warm water where temperature effects on physiology dominate. This may suggest that major differences exist among locomotory capacities of larval fish that inhabit cold, temperate waters compared to those that live in warm tropical waters. It is possible that fish larvae may have developed strategies that affect dispersal and recruitment in different aquatic habitats in order to cope not only with temperature‐induced physiological challenges, but physical challenges as well.     

Shifting the balance between foraging and predator avoidance: the importance of food distribution for a schooling pelagic forager

It is widely held that when predator avoidance conflicts with other activities, such as feeding, avoidance of predators often takes precedence. In this study, we examine how predation risk and food distribution interact to influence the schooling behavior and swimming speed of foraging juvenile walleye pollock, Theragra chalcogramma. Fish were acclimated to either spatially and temporally clumped, or spatially and temporally dispersed food for 3 weeks. Fish were then monitored while feeding in the absence and presence of predatory sablefish, Anoplopoma fimbria. Fish foraging for clumped food swam rapidly in a loose school when predators were absent, but swam more slowly and adopted more cohesive schooling in the presence of predators, trading-off foraging opportunity for decreased vulnerability to predators. Fish foraging for dispersed food swam about slowly and did not engage in cohesive schooling in either the absence or presence of predators. These fish accepted greater predation risk in order to continue foraging, suggesting that the cost of schooling, in terms of decreased foraging opportunity, was greater when food was dispersed than when it was clumped. This lower responsiveness to predators among fish receiving dispersed food demonstrates that predator avoidance does not always take precedence over other activities, but rather, that a balance is maintained between predator avoidance and feeding, which shifts as food distribution changes.     

Transitions in functional morphology from “large branchiopods” to Cladocera: Video and confocal microscopic studies of Cyclestheria hislopi (Cyclestherida) and Sida crystallina (Cladocera: Ctenopoda)

Great diversity is found in morphology and functionality of arthropod appendages, both along the body axis of individual animals and between different life-cycle stages. Despite many branchiopod crustaceans being well known for displaying a relatively simple arrangement of many serially post-maxillary appendages (trunk limbs), this taxon also shows an often unappreciated large variation in appendage morphology. Diplostracan branchiopods exhibit generally a division of labor into locomotory antennae and feeding/filtratory post-maxillary appendages (trunk limbs). We here study the functionality and morphology of the swimming antennae and feeding appendages in clam shrimps and cladocerans and analyze the findings in an evolutionary context (e.g., possible progenetic origin of Cladocera). We focus on Cyclestheria hislopi (Cyclestherida), sister species to Cladocera and exhibiting many “large” branchiopod characters (e.g., many serially similar appendages), and Sida crystallina (Cladocera, Ctenopoda), which likely exhibits plesiomorphic cladoceran traits (e.g., six pairs of serially similar appendages). We combine (semi-)high-speed recordings of behavior with confocal laser scanning microscopy analyses of musculature to infer functionality and homologies of locomotory and filtratory appendages in the two groups. Our morphological study shows that the musculature in all trunk limbs (irrespective of limb size) of both C. hislopi and S. crystallina comprises overall similar muscle groups in largely corresponding arrangements. Some differences between C. hislopi and S. crystallina, such as fewer trunk limbs and antennal segments in the latter, may reflect a progenetic origin of Cladocera. Other differences seem related to the appearance of a specialized type of swimming and feeding in Cladocera, where the anterior locomotory system (antennae) and the posterior feeding system (trunk limbs) have become fully separated functionally from each other. This separation is likely one explanation for the omnipresence of cladocerans, which have conquered both freshwater and marine free water masses and a number of other habitats.     

Survival selection on escape performance and its underlying phenotypic traits: a case of many‐to‐one mapping

Selection often operates not directly on phenotypic traits but on performance which is important as several traits may contribute to a single performance measure (many‐to‐one mapping). Although largely ignored in the context of selection, this asks for studies that link all relevant phenotypes with performance and fitness. In an enclosure experiment, we studied links between phenotypic traits, swimming performance and survival in two Enallagma damselflies. Predatory dragonflies imposed survival selection for increased swimming propensity and speed only in E. annexum; probably E. aspersum was buffered by the former species’ presence. Accordingly, more circular caudal lamellae, structures involved in generating thrust while swimming, were selected for only in E. annexum. Other phenotypic traits that contributed to swimming speed were apparently not under selection, probably because of many‐to‐one mapping (functional redundancy). Our results indicate that not only the phenotypic distributions of syntopic prey organisms but also many‐to‐one mapping should be considered when documenting phenotype–performance–fitness relationships.     

The effects of starvation and repeated disturbance on mass loss,pit construction,and spatial pattern in a trap‐building predator

1. Starvation tolerance is an important trait for animals, as most will encounter starvation within their lifetime. Sit‐and‐wait predators are better adapted to starvation owing to their naturally low encounter rate with prey. 2. Starvation tolerance was studied under three levels of disturbance of wormlion larvae, a strict sit‐and‐wait predator that constructs pits. 3. Frequently disturbed wormlions constructed pits less often, and larger individuals continued to construct pits more frequently than smaller ones. It was expected that a high disturbance level would lead to a high rate of mass loss, however, surprisingly, the rate of mass loss was not higher for the frequently disturbed group. This suggests that the energetic cost of pit construction and maintenance is not as high as previously suggested for other pit‐building predators. 4. Larger individuals tolerated starvation better, in losing a lower proportion of their initial body mass and having higher chances of survival throughout the experiment. 5. The effect of starvation on the distance to neighbours was also investigated, and starved individuals were expected to maximise this distance in order to avoid interference competition. However, wormlions were usually clumped, and starvation or feeding had no effect on the pits' spatial pattern, suggesting that interference competition plays a minor role in this species. 6. Generally, wormlion larvae demonstrated a high starvation tolerance and low mortality rates even after 9 weeks of starvation.