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1.
  1. Native freshwater mussels are a guild of benthic, filter feeding invertebrates that perform important ecological functions in rivers. Because of their long lifespans (30–50 years or longer), mussels are slow to respond to human-induced alterations. Thus, development of sensitive indicators of mussel population responses to river conditions and management would be beneficial. Compared to marine species, estimation of vital rates (e.g. survival, growth) in freshwater mussels has received little attention.
  2. We placed passively integrated transponder tags on 578 mussels of four species (Amblema plicata, Cyclonaias pustulosa, Obliquaria reflexa, and Pleurobema sintoxia) in a well-studied mussel assemblage in a side channel of the upper Mississippi River. Growth and survival of tagged mussels were assessed annually for 4 years across core (high density) and peripheral (low density) areas of the assemblage.
  3. Overall survival was highly variable, ranging from c. 15 to 90%, and was related to life history, habitat quality, and hydrologic events. Survival, which varied significantly among species and over time, was consistently higher in the dense and species-rich core of the mussel assemblage, relative to the periphery because substrates were consistently more stable in the core of the mussel bed relative to the periphery. Substrate movement during low flows was an order of magnitude lower in the core relative to the periphery, and survival was inversely related to stability of river substrates. Patterns in habitat-specific survival indicate source–sink population dynamics such that mussels in the core habitat provide recruitment to the periphery, but mussels in the periphery are subject to unsustainably low survival; additional studies to track the source of recruitment in the periphery are needed to test this hypothesis.
  4. Growth rate did not vary significantly between core and peripheral areas but did vary by species. Growth rate (proportional change per year) declined with age, and was similar at mean age for A. plicata (0.016 per year), P. sintoxia (0.015 per year), and C. pustulosa (0.013 per year), but much lower for O. reflexa (0.008 per year).
  5. Effective management decisions for mussels requires a better understanding of how vital rates govern populations and how they vary across a suite of physical and biological factors. Information on how population vital rates vary among species and over time gives managers another tool to understand how mussels may respond to management actions such as habitat restoration projects. Given the importance of substrate stability inferred from this study, management actions that maintain or increase substrate stability are likely to result in high quality mussel assemblages and may restore a valuable component of ecosystem function in this region.
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River impoundments can fundamentally restructure downstream fish assemblages by altering flow regimes. However, the degree of alteration and associated ecological change may depend on pre-existing hydrologic regimes. We used long-term datasets to compare downstream hydrological and fish assemblage responses to impoundment in two catchments classified as having intermittent and perennial-flashy natural hydrologic regimes. We observed significant shifts in fish assemblage structure at both sites after stream impoundment. The historically intermittent stream shifted to a stable perennial flow regime. Changes in fish assemblage structure covaried with changes in five different components of the flow regime; most species that increased in abundance require fluvial habitats and likely benefited from increased flows during historically low flow seasons. Shifts in fish assemblage structure were also observed in the perennial stream, despite minimal flow alteration after impoundment; however, most species shifts were associated with lentic environments, and were more likely related to proximity of reservoirs in the drainage system rather than changes in stream flow. Findings from this study confirm that downstream fish assemblage response to river impoundment can be associated with high levels of hydrologic alteration, but other factors including expansion of lentic species into lotic environments also influence shifts in assemblage structure.  相似文献   

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Fish assemblage structure, rarefied species richness, species diversity and evenness of assemblages upstream of a reservoir in Oklahoma, U.S.A., were compared pre and post‐impoundment as well as in contemporary collections from streams above and below the reservoir. There were significant shifts in assemblage structure between historical and contemporary collections above the reservoir but not between contemporary assemblages above and below the impoundment. Indicator species analysis revealed that the sand shiner Notropis stramineus and fathead minnow Pimephales promelas have declined, whereas largemouth bass Micropterus salmoides and western mosquitofish Gambusia affinis have increased in relative abundance in assemblages upstream of the impoundment. Species richness was lower in contemporary assemblages compared with historical assemblages. Furthermore, contemporary assemblages below the dam had lower species richness, diversity and evenness compared with contemporary collections above the dam. These results highlight the spatial and temporal extent of reservoirs altering fish assemblages upstream of impoundments.  相似文献   

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  • 1 Effective environmental management requires a sound understanding of the causal mechanisms underlying the relationship of species with their environment. Mechanistic explanations linking species and environment are ultimately based on species traits. Many tools for ecological assessment and biomonitoring lack such explanations. Elsewhere, we have defined life‐history strategies, based on the interrelations between species traits and their functional implications.
  • 2 This study tests the hypothesis that life‐history strategies represent different solutions to particular ecological problems, thus connecting species and their environment through species traits. Data on aquatic macroinvertebrates in a variety of waterbodies were analysed in terms of life‐history strategies. These waterbodies differed in environmental conditions and macroinvertebrate assemblages. Solutions to the ecological problems present in each type of water body were expected to be reflected in the abundance of (species exhibiting) different life‐history strategies.
  • 3 Results show clear differences in strategy composition between the different water types, which could be related to the prevailing environmental conditions through mechanistic explanations. For example, species with a long period of juvenile development and a synchronized emergence of short‐lived adults were most dominant in large mesotrophic waterbodies with stable and predictable environmental conditions. In contrast, species that have a rapid development and spread successive reproduction attempts over a longer time period were most abundant in waterbodies with fluctuating and less predictable environmental conditions.
  • 4 Differences in strategy composition provide insight into the prevailing environmental conditions related to temporal predictability, and habitat favourability, from the perspective of the species themselves. By reducing diverse species assemblages to a small number of strategies, representing easily interpretable relationships, this approach may be useful in environmental quality assessment programmes, including those required by the European Water Framework Directive. Based on mechanistic explanations, life‐history strategies may generate testable predictions and guide future research. Further research may focus on expanding life‐history strategies to include other species groups and ecosystems.
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Beetle assemblages in ponds: effects of habitat and site age   总被引:11,自引:1,他引:10  
  • 1 Water beetle assemblages were sampled in each of 18 freshwater ponds, including 11 recently constructed sites designed to provide mitigation for wetlands destruction elsewhere, and seven older reference sites. There were three objectives: (a) to relate taxon richness and biomass of the beetles to the same properties of the wider aquatic invertebrate community, (b) to evaluate changes in beetle assemblage structure over time, and (c) to determine habitat effects on taxonomic composition, mean body size and trophic guild structure of the beetle assemblage.
  • 2 Forty‐seven beetle genera were identified, representing 77 species. The beetles represented an average of 21.5% of total generic richness, but only 3.7% of total wet biomass of the wider invertebrate community.
  • 3 Of all variables evaluated using canonical correspondence analysis (CCA), site age had the greatest influence on the beetle assemblage. Predatory dytiscids were early colonists at younger sites, while herbivorous curculionids and chrysomelids associated with particular types of vegetation typically occurred in older ponds. Mitigation ponds and reference ponds supported similar numbers of species. Reference sites, however, harboured substantially more unique species found at only a single site within the study area.
  • 4 The presence of fish was also strongly related to beetle assemblage structure. Ponds with few or no fish contained about 3‐fold higher biomass and 3‐fold greater mean wet weight per individual compared to ponds with substantial fish assemblages.
  • 5 Beetle assemblage composition varied among sites and sampling years, but beetle biomass, richness and species composition may be useful tools in evaluating the success of wetland mitigation efforts.
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  1. Assemblages of insect herbivores are structured by plant traits such as nutrient content, secondary metabolites, physical traits, and phenology. Many of these traits are phylogenetically conserved, implying a decrease in trait similarity with increasing phylogenetic distance of the host plant taxa. Thus, a metric of phylogenetic distances and relationships can be considered a proxy for phylogenetically conserved plant traits and used to predict variation in herbivorous insect assemblages among co‐occurring plant species.
  2. Using a Holarctic dataset of exposed‐feeding and shelter‐building caterpillars, we aimed at showing how phylogenetic relationships among host plants explain compositional changes and characteristics of herbivore assemblages.
  3. Our plant–caterpillar network data derived from plot‐based samplings at three different continents included >28,000 individual caterpillar–plant interactions. We tested whether increasing phylogenetic distance of the host plants leads to a decrease in caterpillar assemblage overlap. We further investigated to what degree phylogenetic isolation of a host tree species within the local community explains abundance, density, richness, and mean specialization of its associated caterpillar assemblage.
  4. The overlap of caterpillar assemblages decreased with increasing phylogenetic distance among the host tree species. Phylogenetic isolation of a host plant within the local plant community was correlated with lower richness and mean specialization of the associated caterpillar assemblages. Phylogenetic isolation had no effect on caterpillar abundance or density. The effects of plant phylogeny were consistent across exposed‐feeding and shelter‐building caterpillars.
  5. Our study reveals that distance metrics obtained from host plant phylogeny are useful predictors to explain compositional turnover among hosts and host‐specific variations in richness and mean specialization of associated insect herbivore assemblages in temperate broadleaf forests. As phylogenetic information of plant communities is becoming increasingly available, further large‐scale studies are needed to investigate to what degree plant phylogeny structures herbivore assemblages in other biomes and ecosystems.
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  1. Animals contribute significantly to nutrient cycling through excretion, but most studies consider their effects under relatively benign abiotic conditions. Disturbances such as drought may alter animals’ nutrient contributions through shifts in species composition and biomass. Headwater streams are particularly vulnerable to extreme climate events and thus might show rapid changes in stream biota and their ecosystem effects.
  2. We tested how biomass and subsequent ecosystem effects (nutrient cycling) of an intermittent prairie stream community changed during a drought. We quantified the biomass and contributions to nutrient cycling for assemblages comprising fishes, crayfish, and tadpoles in 12 isolated pools over 3 months encompassing the harshest drought on record for Kings Creek, KS, U.S.A. We predicted that macroconsumer biomass would decline with pool surface area and that differences in macroconsumer biomass and taxonomic composition would lead to different contributions of pool assemblages to nutrient cycling.
  3. The biomass of pool assemblages declined with decreasing pool size, a pattern apparently driven by mortality, emigration, or metamorphosis. We also observed a change in assemblage structure of drying pools during drought relative to pool size, shifting dominance toward species with more drought-resistant traits. Accordingly, assemblage nitrogen (N) excretion rates declined as pool biomass was reduced, leading to a 58% reduction in N available to epilithic biofilms. Phosphorus (P) excretion rates declined from June to July, but increased in August, as species with high P excretion rates maintained similar proportional biomass and biomass of a non-native fish increased. Molar N:P of pool assemblage excretion declined significantly throughout the drought and coincided with loss of southern redbelly dace (Chrosomus erythrogaster: Cyprinidae).
  4. Animal-mediated nutrient cycling was altered by the loss of biomass and stoichiometric traits of taxa that differed in their occurrences and ability to tolerate abiotic conditions during drought. Elevated availability of dissolved N in isolated pools may increase N uptake rates by biofilms during drought conditions, indicating the importance of N excreted by aggregated macroconsumers, especially those with unique stoichiometric traits. While the significance of shifts in the composition of freshwater communities to ecosystems is not entirely known, additional losses in ecosystem function and changes in community structure may follow episodes of severe drought.
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  1. Spatial grain of studies of communities is often based on arbitrary convention. Few studies have examined how spatial scaling of grain size affects estimates of compositional change over time, despite its broad implications.
  2. Fish assemblage structure was compared between 1974 and 2014 at 33 sampling locations in the Muddy Boggy River drainage, USA. The two main objectives for this comparison were to quantify change in assemblage structure and to test for a relationship between compositional change and spatial scale. Spatial scale was manipulated by pooling assemblage data into a continuous range of groups, which increased in size from K = 33 pairs (i.e., local scale) to K = 1 pair (i.e., global scale), via clustering algorithm based on pair‐wise fluvial distance.
  3. Local assemblages (stream reaches) varied in the degree of assemblage change over time (range = 0.10–0.99 dissimilarity; mean = 0.66). The global assemblage (drainage), however, remained relatively similar. A discontinuity in the relationship between compositional change and spatial scale occurred at K = 15 (mean dissimilarity = 0.56; p = .062), and this grouping is roughly the size of the headwater/tributary drainages (i.e., stream order ≤ 3) in the study system.
  4. Spatial scale can impact estimates of biodiversity change over time. These results suggest assemblages are more dynamic at individual stream reaches than at the scale of the entire drainage. The decline in assemblage change at the spatial scale of K = 15 deserves further attention given the marginal significance, despite a small sample size (n = 15). This pattern could suggest regional and meta‐community processes become more important in shaping assemblage dynamics at the scale of headwater drainages, whereas the factors responsible for driving individual stream reach dynamics (e.g., stochasticity) become less important. Defining assemblages at a larger scale will result in different estimates of species persistence. Biodiversity monitoring efforts must take the effect of spatial scaling into consideration.
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  1. Habitat fragmentation is one of the main threats to biodiversity. Barriers to dispersal caused by anthropogenic habitat alteration may affect phylogeographic patterns in freshwater mussels. Knowledge of the phylogenetic and phylogeographic patterns of unionoids is vital to inform protection of their biodiversity.
  2. Here, we assessed influences of dams and their environmental effects on the genetic diversity and population connectivity of a broadly distributed freshwater mussel, Nodularia douglasiae, in Poyang Lake Basin.
  3. The results showed high genetic diversity in areas without dams and low genetic diversity in areas with dams. High genetic differentiation and low gene flow were found among the 11 populations. Genetic variation was significantly correlated with dissolved oxygen levels.
  4. The observation of low genetic diversity in populations separated by dams indicated that those populations were subjected to genetic erosion and demographic decline because they are disconnected from other populations with higher diversity. High genetic differentiation and low gene flow among the 11 populations could be correlated with anthropogenic habitat alteration.
  5. These results indicated that anthropogenic habitat alterations have led to the decline in freshwater mussel diversity. Therefore, we recommend maintaining favourable habitat conditions and connectivity of rivers or lakes, and strengthening study of life histories with host-test experiments to identify potential host fish species to strengthen the knowledge base underpinning freshwater mussel conservation.
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Life-history strategies in freshwater macroinvertebrates   总被引:1,自引:0,他引:1  
  • 1 Explaining spatial and temporal differences in species assemblages is a central aim of ecology. It requires a sound understanding of the causal mechanisms underlying the relationship of species with their environment. A species trait is widely acknowledged to be the key that links pattern and process, although the enormous variety of traits hampers generalization about which combination of traits are adaptive in a particular environment.
  • 2 In three steps, we used species traits to match species and environment, and chose lentic freshwater ecosystems to illustrate our approach. We first identified key environmental factors and selected the species traits that enable the organism to deal with them. Secondly, we investigated how investments in these traits are related (e.g. through trade‐offs). Thirdly, we outlined 13 life‐history strategies, based on biological species traits, their interrelations known from life‐history theory and their functional implications.
  • 3 Species traits and environmental conditions are connected through life‐history strategies, with different strategies representing different solutions to particular ecological problems. In addition, strategies may present an integrated response to the environment as they are based on many different traits and their interrelationships. The presence and abundance of (species exhibiting) different life‐history strategies in a location may therefore give direct information about how a particular environment is experienced by the species present.
  • 4 Life‐history strategies can be used to (i) explain differences in species assemblages either between locations or in different periods; (ii) compare waterbodies separated by large geographical distances, which may comprise different regional species pools or span species distribution areas and (iii) reduce often very complex, biodiverse assemblages into a few meaningful, easily interpretable relationships.
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  1. South Africa is a megadiverse country. Here, natural communities are unevenly distributed across, and within, seven distinct biomes. In such heterogeneous landscapes, understanding spatial patterns of biodiversity is essential for planning and implementing efficient conservation measures.
  2. The southern Kalahari, forming part of South Africa's savanna biome, is an arid region of peculiarly high diversity and endemism. The responses of orthopteran assemblages to changing environmental conditions across the Kalahari were investigated by comparing alpha and beta diversity levels across discrete vegetation types in the Tswalu Kalahari Reserve. The degree of association between species and specific vegetation types were also studied and how a key life history trait - dispersal ability – influences community composition was determined.
  3. This study identified 46 grasshopper species within the reserve, which compares well with richness levels in other more productive habitats of the country. Local (alpha) diversity was higher in mountain and mountain-ecotone sites versus vegetation types on the plains, and species turnover was also exceptionally high – approaching 100% - across these two groups. The few (3) dispersal limited species recovered were associated only with the mountain-ecotone group, with emergent dominance patterns suggesting that competitive rather than dispersal abilities determine the species composition of unique assemblages in the landscape.
  4. Topology plays a key role in maintaining spatial diversity across the southern Kalahari landscape. Mountains, and their ecotones, promote not only species turnover, but also richness and functional diversity. These can be viewed as islands of diversity, and should be targeted priority areas for conservation beyond the boundaries of protected areas.
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