Human society has used freshwater from rivers, lakes, groundwater, and wetlands for many different urban, agricultural, and industrial activities, but in doing so has overlooked its value in supporting ecosystems. Freshwater is vital to human life and societal well‐being, and thus its utilization for consumption, irrigation, and transport has long taken precedence over other commodities and services provided by freshwater ecosystems. However, there is growing recognition that functionally intact and biologically complex aquatic ecosystems provide many economically valuable services and long‐term benefits to society. The short‐term benefits include ecosystem goods and services, such as food supply, flood control, purification of human and industrial wastes, and habitat for plant and animal life—and these are costly, if not impossible, to replace. Long‐term benefits include the sustained provision of those goods and services, as well as the adaptive capacity of aquatic ecosystems to respond to future environmental alterations, such as climate change. Thus, maintenance of the processes and properties that support freshwater ecosystem integrity should be included in debates over sustainable water resource allocation. The purpose of this report is to explain how the integrity of freshwater ecosystems depends upon adequate quantity, quality, timing, and temporal variability of water flow. Defining these requirements in a comprehensive but general manner provides a better foundation for their inclusion in current and future debates about allocation of water resources. In this way the needs of freshwater ecosystems can be legitimately recognized and addressed. We also recommend ways in which freshwater ecosystems can be protected, maintained, and restored. Freshwater ecosystem structure and function are tightly linked to the watershed or catchment of which they are a part. Because riverine networks, lakes, wetlands, and their connecting groundwaters, are literally the “sinks” into which landscapes drain, they are greatly influenced by terrestrial processes, including many human uses or modifications of land and water. Freshwater ecosystems, whether lakes, wetlands, or rivers, have specific requirements in terms of quantity, quality, and seasonality of their water supplies. Sustainability normally requires these systems to fluctuate within a natural range of variation. Flow regime, sediment and organic matter inputs, thermal and light characteristics, chemical and nutrient characteristics, and biotic assemblages are fundamental defining attributes of freshwater ecosystems. These attributes impart relatively unique characteristics of productivity and biodiversity to each ecosystem. The natural range of variation in each of these attributes is critical to maintaining the integrity and dynamic potential of aquatic ecosystems; therefore, management should allow for dynamic change. Piecemeal approaches cannot solve the problems confronting freshwater ecosystems. Scientific definitions of the requirements to protect and maintain...
Whole-stream metabolism in a first-order stream was measured using upstream–downstream changes in dissolved oxygen (DO) concentration measured at 1-min intervals over a 40-h period. The measured change in DO was corrected for reaeration flux using a reaeration coefficient determined from injections of conservative and volatile tracers. The whole-stream metabolism measurement was compared in the spring with in situ chamber measurements performed a few days later in the same stream reach. Chamber measurements of community respiration extrapolated to a 24-h period (CR24) were about one third the whole-stream measurements, while gross primary production (GPP) measured at midday in the chambers was roughly 20% less than the whole-stream estimate. Whole-stream GPP was higher during the spring just prior to forest canopy closure than in summer or autumn. Community respiration exceeded whole-stream GPP on all dates and was greatest during the summer. Our results suggest that this whole-stream approach provides a measure of total stream metabolism that is relevant to other stream ecosystem processes measured on reach scales, such as nutrient spiralling.
With increasing pressure placed on natural systems by growing human populations, both scientists and resource managers need a better understanding of the relationships between cumulative stress from human activities and valued ecosystem services. Societies often seek to mitigate threats to these services through largescale, costly restoration projects, such as the over one billion dollar Great Lakes Restoration Initiative currently underway. To help inform these efforts, we merged high-resolution spatial analyses of environmental stressors with mapping of ecosystem services for all five Great Lakes. Cumulative ecosystem stress is highest in nearshore habitats, but also extends offshore in Lakes Erie, Ontario, and Michigan. Variation in cumulative stress is driven largely by spatial concordance among multiple stressors, indicating the importance of considering all stressors when planning restoration activities. In addition, highly stressed areas reflect numerous different combinations of stressors rather than a single suite of problems, suggesting that a detailed understanding of the stressors needing alleviation could improve restoration planning. We also find that many important areas for fisheries and recreation are subject to high stress, indicating that ecosystem degradation could be threatening key services. Current restoration efforts have targeted high-stress sites almost exclusively, but generally without knowledge of the full range of stressors affecting these locations or differences among sites in service provisioning. Our results demonstrate that joint spatial analysis of stressors and ecosystem services can provide a critical foundation for maximizing social and ecological benefits from restoration investments.Laurentian Great Lakes | cumulative impact | marine spatial planning | fresh water
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In this study we examined the role of nutrient cycling and herbivory in regulating stream periphyton communities. Population, community, and ecosystem—level properties were studied in laboratory stream channels that had nutrient inputs reduced compared to channels where ambient nutrient levels were maintained. We reduced nutrient inputs in four of eight channels by recirculating 90% of the flow, whereas the other four channels received once—through flow of spring water. We examined the interaction between herbivory and nutrients by varying the number of snails (Elimia clavaeformis) among streams with different nutrient input (circulation) regimes. Reduction in nutrient input viar recirculation resulted in lower concentrations of nutrients in the water but did not result in significant differences in biomass, carbon fixation, or algal taxonomic composition. However, herbivory had large effects on these characteristics by reducing biomass and areal rates of carbon fixation and simplifying periphyton taxonomy and physiognomy. Lower rates of nutrient input significantly affected characteristics associated with nutrient cycling. Streams with reduced nutrient inputs had lower periphyton nutrient contents, higher ratios of total : net uptake of P from water, and higher rates of phosphatase activity than streams with ambient nutrient inputs. However, the effects of reduced nutrient input on cycling characteristics were reduced or eliminated by intense herbivory. Our results indicate that nutrient cycling can increase in response to reductions in nutrient input once sufficient biomass or detritus accumulates to facilitate cycling, thereby allowing biomass accrual and carbon fixation rates to be maintained at levels achieved at higher nutrient inputs. In streams with low nutrient input, cycling can meet a large fraction of the nutrient demand of the periphyton. Because our experimental design involved a reduction from ambient nutrient levels rather than the usual enrichment techniques (e.g., additions to water, nutrient—diffusing substrates) in aquatic ecosystems, we have been able to observe how biological structure and processes are influenced by external nutrient inputs at the low natural levels of most undisturbed streams.
Periphyton communities have received relatively little attention in lake ecosystems. However, evidence is increasing that they play a key role in primary productivity, nutrient cycling, and food web interactions. This review summarizes those findings and places them in a conceptual framework to evaluate the functional importance of periphyton in lakes. The role of periphyton is conceptualized based on a spatial hierarchy. At the coarsest scale, landscape properties such as lake morphometry, influence the amount of available habitat for periphyton growth. Watershed-related properties, such as loading of dissolved organic matter, nutrients, and sediments influence light availability and hence periphyton productivity. At the finer scale of within the lake, both habitat availability and habitat type affect periphyton growth and abundance. In addition, periphyton and phytoplankton compete for available resources at the within-lake scale. Our review indicates that periphyton plays an important functional role in lake nutrient cycles and food webs, especially under such conditions as relatively shallow depths, nutrient-poor conditions, or high water-column transparency. We recommend more studies assessing periphyton function across a spectrum of lake morphometry and trophic conditions.
To investigate the influence of plant productivity on plant-herbivore interactions in stream ecosystems, we varied the productive capacity of algal assemblages by exposing periphyton to three levels of irradiance and two levels of grazing. We studied interactions between algal assemblages (grown from algae obtained from four Oregon streams) and herbivorous snails (Juga silicula) in 15 laboratory streams containing either 250 snails/m 2 or no snails. Biomass, production, export, and taxonomic structure of the algal community were measured at intervals throughout the 75-d study. Ingestion rate and assimilation efficiency of snails also were measured on six different dates using dual-isotope labeling, and snail growth was measured at the end of the experiment.Rates of primary production, algal biomass accumulation, and dominance by chlorophytes generally increased with higher irradiance, although these patterns were modified by herbivores. Ungrazed periphyton at low irradiance (photon flux density: 20 ~mol·m-2 • s-1 ) accumulated little biomass, which was further reduced by grazing snails. At intermediate (100 ~mol·m-2 ·s-1 ) and high (400 ~mol·m-2 ·s-1 ) irradiance, snails delayed the accumulation of algal biomass but did not affect the final biomass attained. After 43 d, net primary production (NPP) at high irradiance was unaffected by grazing, whereas grazing increased NPP at both low and intermediate irradiance. Algal export increased with both irradiance and the presence of grazers and constituted a significant loss of plant biomass from the streams. Grazing by Juga delayed algal succession and altered algal taxonomic structure and assemblage physiognomy by reducing the relative abundance of erect and non-attached algae, while increasing the abundance of adnate diatoms.Snails grew slowly at low irradiance, due to scant food resources, but had high growth rates at intermediate and high irradiance, probably because food was not limiting. Assimilation efficiencies for snails generally varied from 40 to 70% and were highest at low irradiance. At low irradiance, 90% of benthic production was harvested by grazers, whereas only 10% accumulated as attached biomass or was exported. At higher irradiances, < 15% of primary production was harvested by grazers, and >85% persisted as attached algae or was exported.In these stream ecosystems, the biomass and production of grazers were influenced by abiotic constraints placed on algal productive capacity (i.e., the ability of a plant assemblage to generate biomass). The structure and metabolism of algal assemblages were affected, in turn, by consumptive demand of herbivores. The productive capacity ofperiphyton modified the nature and outcome of plant-herbivore interactions. This capacity therefore has important implications for the operation of stream ecosystems.
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