Behavioural activity levels and expression of stress proteins under predation risk in two damselfly species

Abstract 1. It has become apparent that predators may strongly decrease prey fitness without direct contact with the prey, as they induce the development of defence systems that limit the availability of energy for growth and reproduction. Recent studies suggest that stress proteins may help prey organisms deal with this stress. The pattern is not general, however, and little is known about species differences in physiological traits in coping with predator stress, and covariation of physiological with other antipredator traits. 2. To explore these issues, we quantified levels of constitutive and fish‐induced stress proteins (Hsp60 and Hsp70) and anti‐predator behaviours in larvae of two damselfly species that differ in lifestyle. Both stress proteins were fixed at higher levels in Erythromma najas, which has a slow lifestyle, than in Lestes sponsa, which has a fast lifestyle. Similarly, anti‐predator behaviours were fixed at safer levels in E. najas than in L. sponsa. 3. These results suggest that stress proteins may be part of anti‐predator syndromes of damselfly larvae, and there may be trait co‐specialisation between stress proteins and behavioural anti‐predator traits. Studies formally testing these hypotheses in more species may prove rewarding in advancing our understanding of the functional integration of physiological anti‐predator traits in relation to the prey’s lifestyle.     

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.     

Daphnia community analysis in shallow Kenyan lakes and ponds using dormant eggs in surface sediments

1. Water fleas of the genus Daphnia are considered rare in tropical regions, and information on species distribution and community ecology is scarce and anecdotal. This study presents the results of a survey of Daphnia species distribution and community composition in 40 standing waterbodies in southern Kenya. The study sites cover a wide range of tropical standing aquatic habitats, from small ephemeral pools to large permanent lakes between approximately 700 and 2800 m a.s.l. Our analysis combines data on Daphnia distribution and abundance from zooplankton samples and dormant eggs in surface sediments. 2. Nearly 70% (27 of 40) of the sampled waterbodies were inhabited by Daphnia. Although their abundance in the active community was often very low, this high incidence shows that Daphnia can be equally widespread in tropical regions as in temperate regions. 3. Analysis of local species assemblages from dormant eggs in surface sediments was more productive than snapshot sampling of zooplankton communities. Surface‐sediment samples yielded eight Daphnia species in total, and allowed the detection of Daphnia in 25 waterbodies; zooplankton samples revealed the presence of only four Daphnia species in 16 waterbodies. 4. Daphnia barbata, D. laevis, and D. pulex were the most frequently recorded and most abundant Daphnia species. Canonical correspondence analysis of species–environment relationships indicates that variation in the Daphnia community composition of Kenyan waters was best explained by fish presence, temperature, macrophyte cover and altitude. Daphnia barbata and D. pulex tended to co‐occur with each other and with fish. Both species tended to occur in relatively large (>10 ha) and deeper (>2 m) alkaline waters (pH 8.5). Daphnia laevis mainly occurred in cool and clear, macrophyte‐dominated lakes at high altitudes.     

A cryptic invasion within an invasion and widespread introgression in the European water frog complex: consequences of uncontrolled commercial trade and weak international legislation

In Western Europe, many pond owners introduce amphibians for ornamental purposes. Although indigenous amphibians are legally protected in most European countries, retailers are circumventing national and international legislation by selling exotic nonprotected sibling species. We investigated to what extent non‐native species of the European water frog complex (genus Pelophylax) have become established in Belgium, using morphological, mitochondrial and nuclear genetic markers. A survey of 87 sampling sites showed the presence of non‐native water frogs at 47 locations, mostly Marsh frogs (Pelophylax ridibundus). Surprisingly, at least 19% of all these locations also harboured individuals with mitochondrial haplotypes characteristic of Anatolian water frogs (Pelophylax cf. bedriagae). Nuclear genotyping indicated widespread hybridization and introgression between P. ridibundus and P. cf. bedriagae. In addition, water frogs of Turkish origin obtained through a licensed retailer, also contained P. ridibundus and P. cf. bedriagae, with identical haplotypes to the wild Belgian populations. Although P. ridibundus might have invaded Belgium by natural range expansion from neighbouring countries, our results suggest that its invasion was at least partly enhanced by commercial trade, with origins as far as the Middle East. Also the invasion and rapid spread of Anatolian lineages, masked by their high morphological similarity to P. ridibundus, is likely the result of unregulated commercial trade. We expect that Anatolian frogs will further invade the exotic as well as the native range of P. ridibundus and other Pelophylax species elsewhere in Western and Central Europe, with risks of large‐scale hybridization and introgression.     

Hatching of Daphnia sexual eggs. I. Intraspecific differences in the hatching responses of D. magna eggs

• 1 To test the hypothesis that the variability in hatching response of the sexual eggs of Daphnia has a genetic component, hatching after a standardized decapsulation technique was studied in different D. magna families, resulting from intra- as well as interclonal crosses.
• 2 There were significant differences in hatching response between families. Average hatching rates ranged from 0.0% to 81.9%, depending on the family under study.
• 3 Offspring-on-parent regressions indicate that the hatching rate-of sexual eggs is to a large extent determined by the genotype of the mother (maternal inheritance).
• 4 Our results suggest that there is ample generic variation on a microgeographic scale for characteristics related to hatching of sexual eggs in Daphnia.

     

The relative importance of dispersal and local processes in structuring phytoplankton communities in a set of highly interconnected ponds

1. The recognition that both local and regional processes act together in shaping local communities makes determining their relative roles in natural communities central to understanding patterns in community structure. 2. We investigated the relative influence of these processes on the phytoplankton communities of a highly interconnected pond system. We sampled the phytoplankton communities of 28 ponds concurrently with 20 local environmental variables. 3. We found that phytoplankton community variation, in terms of both phytoplankton community composition (PCC) and diversity, was only significantly explained by local environmental variables. These were mainly associated with the contrasting clear‐water and turbid ecological states of the shallow ponds studied. Clear‐water conditions favoured only a few taxa, resulting in a significantly lower taxon diversity and richness under these conditions. 4. The failure to explain variation in PCC by a dispersal model based on the water flow between ponds points at very effective species sorting. This is attributed to the high population turn‐over rates and sensitivity to environmental conditions of phytoplankton communities. Some evidence was found, however, that dispersal influences local communities through mass effects between neighbouring ponds. 5. Overall, our results emphasize both the strong selection pressure that components of the food web exert on phytoplankton communities and the high potential of these communities to respond to such environmental change, thereby effectively opposing the homogenizing effects of continuous dispersal.     

Assembly of zooplankton communities in newly created ponds

1. The creation or severe disturbance of habitat patches is generally followed by a phase of community (re)assembly. After such an event, the trajectory of community assembly in habitat patches may be highly variable because of stochasticity during the dispersal and colonization process. Conversely, assembly patterns may also be deterministic if communities are shaped by prevalent environmental conditions in the habitat patches (species sorting), or by systematic differences in the dispersal capacities of species. 2. In this study, we investigated the pattern of community assembly of zooplankton species in 25 newly created ponds at 13 different sites in Flanders (Belgium). Over a period of three consecutive years, we assessed at what rate and with what frequency species of the regional species pool colonized the newly created ponds. We also studied the development of community structure over time and tested whether the dynamics were consistent across different ponds at the different locations. In addition, we characterized the dynamics of metacommunity features, such as alpha, beta and gamma diversity in clusters of ponds. 3. Even within the first year after their creation, the new ponds were rapidly colonized by a small subset of species from the regional species pool (Daphnia obtusa, Chydorus sphaericus and Simocephalus vetulus). These species dominated the cladoceran assemblages during the subsequent years. Other species in the regional species pools were only sporadically able to colonize ponds. 4. During the entire study period, we observed no significant shifts in species lists or in the occurrences of species among years. The low incidence of the majority of species may be the result of dispersal limitation or the failure of immigrants to establish due to priority effects exerted by the first colonizers. There was, nevertheless, a consistent change in the relative abundance of species, which was most probably mediated by differences in the hatching time among species influencing species composition in the first year. 5. In contrast to expectations, we observed no increase in average alpha diversity (local species richness) and gamma diversity (total richness of entire pond clusters) during the course of the study period. Beta diversity was relatively low from the beginning and remained constant throughout the study period. These deterministic patterns can mainly be attributed to the dominance of the three first colonizing species and the low success rate of other species in colonizing the ponds.     

Conservation of the introgressed European water frog complex using molecular tools

In Belgium, the Pelophylax esculentus complex has recently been subjected to multiple introductions of non-native water frogs, increasing the occurrence of hybridisation events. In the present study, we tested the reliability of morphometric and recently developed microsatellite tools to identify introgression and to determine the origin of exotic Belgian water frogs. By analysing 150 individuals of each taxon of the P. esculentus complex and an additional 60 specimens of the introduced P. cf. bedriagae , we show that neither of the currently available tools appears to have sufficient power to reliably distinguish all Belgian water frog species. We therefore aimed at increasing the discriminatory power of a microsatellite identification tool by developing a new marker panel with additional microsatellite loci. By adding only two new microsatellite loci (RlCA5 and RlCA1b20), all taxa of the P. esculentus complex could be distinguished from each other with high confidence. Three more loci (Res3, Res5 and Res17) provided a powerful discrimination of the exotic species.