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Creators/Authors contains: "Hopper, Garrett_W"

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  1. Abstract The gut microbiome is influenced by host species and the environment, but how the environment influences the microbiome of animals introduced into a new ecosystem has rarely been investigated. Freshwater mussels are aquatic fauna, with some threatened or endangered species propagated in hatcheries and introduced into natural systems as part of conservation efforts. The effects of the environment on the freshwater mussel gut microbiome were assessed for two hatchery-propagated species (Lampsilis ovata, Lampsilis ornata) introduced into rivers within their natural range. Mussels were placed in rivers for 8 weeks, after which one subset was collected, another subset remained in that river, and a third subset was reciprocally transplanted to another river in the same river basin for a further 8 weeks. Gut microbiome composition and diversity were characterized for all mussels. After the initial 8 weeks, mussels showed increased gut bacterial species richness and distinct community composition compared to hatchery mussels, but gut microbiome diversity then decreased for mussels that remained in the same river for all 16 weeks. The gut bacterial community of mussels transplanted between rivers shifted to resemble that of mussels placed initially into the recipient river and that remained there for the whole study. All mussels showed high proportions of Firmicutes in their gut microbiome after 8 weeks, suggesting an essential role of this phylum in the gut of Lampsilis species. These findings show that the mussel gut microbiome shifts in response to new environments and provide insights into conservation strategies that involve species reintroductions. 
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  2. ABSTRACT Freshwater mussels (Bivalvia: Unionida) are among the most imperilled freshwater taxa. Yet, there is a lack of basic life history information for mussels, including data on their growth and longevity. These data help inform conservation efforts, as they can indicate whether species or populations may be vulnerable to decline and inform which species may be best adapted to certain habitats. We aimed to quantify growth and longevity in five mussel species from four river systems in the southeastern United States and test whether growth was related to stream flow. We also interpreted our findings in the context of life history theory.To model mussel growth and longevity, we cut radial thick sections from the shells of mussels and used high‐resolution photography to image the shells. We identified annual growth rings (annuli) and used von Bertalanffy growth models to estimate growth rate (K) and maximum age (Amax) across 13 mussel populations. We then used biochronological methods to remove age‐related variation in annual growth in each shell. We tested whether annual growth was correlated with stream flow using discharge‐based statistics.We found substantial variation inKandAmaxamong species and among populations of the same species.Kwas negatively related toAmax. We did not find consistent correlations between annual growth and stream flow.Our estimates ofKandAmaxalign with previous studies on closely related species and populations. They also match the eco‐evolutionary prediction that growth rate and longevity are negatively related. Life history theory predicts that short‐lived species with higher growth rates should be better adapted to environments with cyclical disturbance regimes, whereas longer‐lived species with low growth rates should be better adapted to stable environments. The lack of correlation between annual growth and stream flow suggests that mussel growth may be limited by other factors in our study system.While some species seem to have relatively narrow ranges for growth and longevity, other species show wide variation among populations. This highlights the need for species‐ and population‐specific conservation efforts. Fundamental life history information can be integrated with other species traits to predict how freshwater taxa may respond to ecological threats. 
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  3. ABSTRACT Emerging aquatic insects can be an important resource subsidy for a variety of terrestrial consumers, including spiders, birds, bats and lizards. Emergence flux is influenced by a variety of abiotic and biotic variables, such as temperature, drying, and predators and these variables can also control the body size of emergent insects. Despite their importance, these variables can change rapidly during drought conditions as water temperatures rise, surface area decreases and predator densities increase.During 2018, the Konza Prairie Biological Station experienced a record drought: flow ceased in the lower reaches of Kings Creek for the first time in over 40 years of observation, leaving a series of isolated pools. We studied how the drought affected aquatic insect emergence in 12 of these pools via elevated temperatures, decreased surface area, and concentration of predators (e.g. fishes and crayfish) over a four‐week period. We returned in 2020 and sampled emergence in the same pools over 2 weeks under non‐drought conditions to compare emergence between drought and non‐drought conditions.We found three overall patterns: (1) rates of areal emergence abundance and biomass (number or mg DM m−2d−1) did not differ between drought and non‐drought conditions. In contrast, pool‐scale emergence abundance, but not biomass (number or mg DM pool−1d−1), was lower during drought conditions; (2) average midge body size was larger during the drought relative to the non‐drought conditions; (3) environmental variables (e.g. temperature, pool surface area, predator biomass) were not predictive of emergence during drought and non‐drought conditions.Fewer, but larger emergent midges (as seen under drought conditions) may represent a higher quality resource for terrestrial consumers than many smaller midges due to increased per‐capita energy yield. However, due to the overall decrease in water availability throughout the stream network, the overall emergence flux was concentrated in reaches with remaining water during the drought, making pools emergence subsidy hotspots. Overall, these contrasting responses underscore the complex nature of community responses to shifting climatic conditions. 
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  4. Abstract Increases in species richness with habitat area (species–area relationship, or SAR) and increases in ecosystem function with species richness (biodiversity–ecosystem functioning, or BEF) are widely studied ecological patterns. Incorporating functional trait analysis into assemblage datasets may help clarify interpretations of SAR and BEF relationships in natural ecological systems. For example, life history theory can be used to make predictions about what species are most important in generating ecosystem function given a certain set of environmental conditions. We used quantitative assemblage data for freshwater mussels at nine sites in western Alabama, USA, to test for SAR and BEF relationships. At each site, we calculated species richness, mussel assemblage density, and two fundamental metrics of ecosystem function: biomass and secondary production. We also tested whether the proportional biomass and production contributions from species belonging to each of three life history strategies—opportunistic strategistsadapted to unstable or frequently disturbed habitats,periodic strategistsadapted to habitats subject to predictable large‐scale disturbances, andequilibrium strategistsadapted to stable habitats—varied longitudinally with stream drainage area, a proxy for habitat area. Species richness increased with stream size (SAR), and both biomass and production increased with species richness (BEF) and mussel density. There were few longitudinal changes in the proportional contributions of the different life history strategy classifications that we used, but the invasive clamCorbicula flumineacontributed proportionally more biomass and production at sites that had smaller drainage areas. This study provides further evidence for a clear longitudinal SAR in stream‐dwelling taxa. It also suggests BEF relationships for biomass and secondary production in natural assemblages but underscores the importance of assemblage density in BEF studies that use observational field data. Variation in proportional biomass and production contributions by different life history strategies was likely limited by the size of the stream size gradient in our study, as contributions were uniformly high for species with life history traits better adapted to stable and productive habitats such as mid‐sized rivers with low or predictable hydrologic disturbance frequencies. This highlights the need to understand how organisms' functional traits govern their relationships to the environment at different scales. 
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