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Edward G. Stets

Publications and source records attributed to Edward G. Stets.

44 records · Page 3Linked to original sources

Long-term trends in alkalinity in large rivers of the conterminous US in relation to acidification, agriculture, and hydrologic modification

Alkalinity increases in large rivers of the conterminous US are well known, but less is understood about the processes leading to these trends as compared with headwater systems more intensively examined in conjunction with acid deposition studies. Nevertheless, large rivers are important conduits of inorganic carbon and other solutes to coastal areas and may have substantial influence on coastal calcium carbonate saturation dynamics. We examined long-term (mid-20th to early 21st century) trends in alkalinity and other weathering products in 23 rivers of the conterminous US. We used a rigorous flow-weighting technique which allowed greater focus on solute trends occurring independently of changes in flow. Increasing alkalinity concentrations and yield were widespread, occurring at 14 and 13 stations, respectively. Analysis of trends in other weathering products suggested that the causes of alkalinity trends were diverse, but at many stations alkalinity increases coincided with decreasing nitrate + sulfate and decreasing cation:alkalinity ratios, which is consistent with recovery from acidification. A positive correlation between the Sen–Thiel slopes of alkalinity increases and agricultural lime usage indicated that agricultural lime contributed to increasing solute concentration in some areas. However, several stations including the Altamaha, Upper Mississippi, and San Joaquin Rivers exhibited solute trends, such as increasing cation:alkalinity ratios and increasing nitrate + sulfate, more consistent with increasing acidity, emphasizing that multiple processes affect alkalinity trends in large rivers. This study was unique in its examination of alkalinity trends in large rivers covering a wide range of climate and land use types, but more detailed analyses will help to better elucidate temporal changes to river solutes and especially the effects they may have on coastal calcium carbonate saturation state.

Science of the Total Environment↗

Inorganic carbon loading as a primary driver of dissolved carbon dioxide concentrations in the lakes and reservoirs of the contiguous United States

Accurate quantification of CO 2 flux across the air-water interface and identification of the mechanisms driving CO 2 concentrations in lakes and reservoirs is critical to integrating aquatic systems into large-scale carbon budgets, and to predicting the response of these systems to changes in climate or terrestrial carbon cycling. Large-scale estimates of the role of lakes and reservoirs in the carbon cycle, however, typically must rely on aggregation of spatially and temporally inconsistent data from disparate sources. We performed a spatially comprehensive analysis of CO 2 concentration and air-water fluxes in lakes and reservoirs of the contiguous United States using large, consistent data sets, and modeled the relative contribution of inorganic and organic carbon loading to vertical CO 2 fluxes. Approximately 70% of lakes and reservoirs are supersaturated with respect to the atmosphere during the summer (June–September). Although there is considerable interregional and intraregional variability, lakes and reservoirs represent a net source of CO 2 to the atmosphere of approximately 40 Gg C d –1 during the summer. While in-lake CO 2 concentrations correlate with indicators of in-lake net ecosystem productivity, virtually no relationship exists between dissolved organic carbon and p CO 2,aq . Modeling suggests that hydrologic dissolved inorganic carbon supports p CO 2,aq in most supersaturated systems (to the extent that 12% of supersaturated systems simultaneously exhibit positive net ecosystem productivity), and also supports primary production in most CO 2 -undersaturated systems. Dissolved inorganic carbon loading appears to be an important determinant of CO 2 concentrations and fluxes across the air-water interface in the majority of lakes and reservoirs in the contiguous United States.

Global Biogeochemical Cycles↗

Carbon dioxide and methane emissions from the Yukon River system

Carbon dioxide (CO 2 ) and methane (CH 4 ) emissions are important, but poorly quantified, components of riverine carbon (C) budgets. This is largely because the data needed for gas flux calculations are sparse and are spatially and temporally variable. Additionally, the importance of C gas emissions relative to lateral C exports is not well known because gaseous and aqueous fluxes are not commonly measured on the same rivers. We couple measurements of aqueous CO 2 and CH 4 partial pressures ( p CO 2 , p CH 4 ) and flux across the water-air interface with gas transfer models to calculate subbasin distributions of gas flux density. We then combine those flux densities with remote and direct observations of stream and river water surface area and ice duration, to calculate C gas emissions from flowing waters throughout the Yukon River basin. CO 2 emissions were 7.68 Tg C yr −1 (95% CI: 5.84 −10.46), averaging 750 g C m −2 yr −1 normalized to water surface area, and 9.0 g C m −2 yr −1 normalized to river basin area. River CH 4 emissions totaled 55 Gg C yr −1 or 0.7% of the total mass of C emitted as CO 2 plus CH 4 and ∼6.4% of their combined radiative forcing. When combined with lateral inorganic plus organic C exports to below head of tide, C gas emissions comprised 50% of total C exported by the Yukon River and its tributaries. River CO 2 and CH 4 derive from multiple sources, including groundwater, surface water runoff, carbonate equilibrium reactions, and benthic and water column microbial processing of organic C. The exact role of each of these processes is not yet quantified in the overall river C budget.

Yukon River Basin↗

The regional abundance and size distribution of lakes and reservoirs in the United States and implication for estimates of global lake extent

We analyzed complete geospatial data for the 3.5 million lakes and reservoirs larger than 0.001 km 2 , with a combined surface area of 131,000 km 2 , in the contiguous United States (excluding the Laurentian Great Lakes) and identified their regional distribution characteristics. For Alaska, we also analyzed (1) incomplete data that suggest that the state contains 1–2.5 million lakes larger than 0.001 km 2 covering over 50,000 km 2 and (2) localized high-resolution (5 m) data that suggest that the number of very small water bodies (< 0.001 km 2 ) may be comparable with the number of lakes > 0.001 km 2 in some areas. The Pareto distribution cannot accurately describe the lake abundance-size relationship across the entire size spectrum, and extrapolation of this density function to small size classes has likely resulted in the overestimation of the number of small lakes in the world. While small water bodies dominate in terms of numbers, they are not numerous enough to dominate in terms of surface area, as has been previously suggested. Extending our results to the global scale suggests that there are on the order of 64 million water bodies larger than 0.001 km 2 in the world, with a total surface area of approximately 3.8 million km 2 .

Limnology and Oceanography↗

Century-scale perspective on water quality in selected river basins of the conterminous United States

Nutrient pollution in the form of excess nitrogen and phosphorus inputs is a well-known cause of water-quality degradation that has affected water bodies across the Nation throughout the 20th century. The recognition of excess nutrients as pollution developed later than the recognition of other water-quality problems, such as waterborne illness, industrial pollution, and organic wastes. Nevertheless, long-term analysis of nutrient pollution is fundamental to our understanding of the current magnitude of the problem, as well the origins and the effects. This report describes the century-scale changes in water quality across a range streams in order to place current water-quality concerns in historical context and presents this history on a national scale as well as for selected river reaches. The primary focus is on nutrient pollution, but the development and societal responses to other water-quality problems also are considered. Land use and agriculture in the selected river reaches also are analyzed to consider how these factors may relate to nutrient pollution. Finally, the availability of relevant nutrient and inorganic carbon data are presented for the selected river reaches. Sources of these data included Federal agencies, State-level reports, municipal public works facilities, public health surveys, and sanitary surveys. The availability of these data extends back more than a century for most of the selected river reaches and suggests that there is a tremendous opportunity to document the development of nutrient pollution in these river reaches.

Scientific Investigations Report↗

Carbon export by rivers draining the conterminous United States

Material exports by rivers, particularly carbon exports, provide insight to basin geology, weathering, and ecological processes within the basin. Accurate accounting of those exports is valuable to understanding present, past, and projected basin-wide changes in those processes. We calculated lateral export of inorganic and organic carbon (IC and OC) from rivers draining the conterminous United States using stream gaging and water quality data from more than 100 rivers. Approximately 90% of land area and 80% of water export were included, which enabled a continental-scale estimate using minor extrapolation. Total carbon export was 41&ndash;49 Tg C yr &minus;1 . IC was >75% of export and exceeded OC export in every region except the southeastern Atlantic seaboard. The 10 largest rivers, by discharge, accounted for 66% of water export and carried 74 and 62% of IC and OC export, respectively. Watershed carbon yield for the conterminous United States was 4.2 and 1.3 g C m &minus;2 yr &minus;1 for IC and OC, respectively. The dominance of IC export was unexpected but is consistent with geologic models suggesting high weathering rates in the continental United States due to the prevalence of easily weathered sedimentary rock.

Inland Waters↗

Dissolved organic carbon export and internal cycling in small, headwater lakes

Carbon (C) cycling in freshwater lakes is intense but poorly integrated into our current understanding of overall C transport from the land to the oceans. We quantified dissolved organic carbon export (DOC X ) and compared it with modeled gross DOC mineralization (DOC R ) to determine whether hydrologic or within-lake processes dominated DOC cycling in a small headwaters watershed in Minnesota, USA. We also used DOC optical properties to gather information about DOC sources. We then compared our results to a data set of approximately 1500 lakes in the Eastern USA (Eastern Lake Survey, ELS, data set) to place our results in context of lakes more broadly. In the open-basin lakes in our watershed ( n = 5), DOC X ranged from 60 to 183 g C m &minus;2 lake area yr &minus;1 , whereas DOC R ranged from 15 to 21 g C m &minus;2 lake area yr &minus;1 , emphasizing that lateral DOC fluxes dominated. DOC X calculated in our study watershed clustered near the 75th percentile of open-basin lakes in the ELS data set, suggesting that these results were not unusual. In contrast, DOC X in closed-basin lakes ( n = 2) was approximately 5 g C m &minus;2 lake area yr &minus;1 , whereas DOC R was 37 to 42 g C m &minus;2 lake area yr &minus;1 , suggesting that internal C cycling dominated. In the ELS data set, median DOC X was 32 and 12 g C m &minus;2 yr &minus;1 in open-basin and closed-basin lakes, respectively. Although not as high as what was observed in our study watershed, DOC X is an important component of lake C flux more generally, particularly in open-basin lakes.

Global Biogeochemical Cycles↗

Quantification of surface water and groundwater flows to open‐ and closed‐basin lakes in a headwaters watershed using a descriptive oxygen stable isotope model

Accurate quantification of hydrologic fluxes in lakes is important to resource management and for placing hydrologic solute flux in an appropriate biogeochemical context. Water stable isotopes can be used to describe water movements, but they are typically only effective in lakes with long water residence times. We developed a descriptive time series model of lake surface water oxygen‐18 stable isotope signature ( δL ) that was equally useful in open‐ and closed‐basin lakes with very different hydrologic residence times. The model was applied to six lakes, including two closed‐basin lakes and four lakes arranged in a chain connected by a river, located in a headwaters watershed. Groundwater discharge was calculated by manual optimization, and other hydrologic flows were constrained by measured values including precipitation, evaporation, and streamflow at several stream gages. Modeled and observed δL were highly correlated in all lakes ( r = 0.84–0.98), suggesting that the model adequately described δL in these lakes. Average modeled stream discharge at two points along the river, 16,000 and 11,800 m 3 d −1 , compares favorably with synoptic measurement of stream discharge at these sites, 17,600 and 13,700 m 3 d −1 , respectively. Water yields in this watershed were much higher, 0.23–0.45 m, than water yields calculated from gaged streamflow in regional rivers, approximately 0.10 m, suggesting that regional groundwater discharge supports water flux through these headwaters lakes. Sensitivity and robustness analyses also emphasized the importance of considering hydrologic residence time when designing a sampling protocol for stable isotope use in lake hydrology studies.

Water Resources Research↗