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At least 973 records · Page 54Linked to original sources

USGS2006

Solute sources in stream water during consecutive fall storms in a northern hardwood forest watershed: A combined hydrological, chemical and isotopic approach

Understanding the effects of climate change including precipitation patterns has important implications for evaluating the biogeochemical responses of watersheds. We focused on four storms in late summer and early fall that occurred after an exceptionally dry period in 2002. We analyzed not only the influence of these storms on episodic chemistry and the role of different water sources in affecting surface water chemistry, but also the relative contributions of these storms to annual biogeochemical mass balances. The study site was a well studied 135-ha watershed in the Adirondack Park of New York State (USA). Our analyses integrated measurements on hydrology, solute chemistry and the isotopic composition of NO 3 − (δ 15 N and δ 18 O) and SO 4 2− (δ 34 S and δ 18 O) to evaluate how these storms affected surface water chemistry. Precipitation amounts varied among the storms (Storm 1: Sept. 14–18, 18.5 mm; Storm 2: Sept. 21–24, 33 mm; Storm 3: Sept. 27–29, 42.9 mm; Storm 4: Oct. 16–21, 67.6 mm). Among the four storms, there was an increase in water yields from 2 to 14%. These water yields were much less than in studies of storms in previous years at this same watershed when antecedent moisture conditions were higher. In the current study, early storms resulted in relatively small changes in water chemistry. With progressive storms the changes in water chemistry became more marked with particularly major changes in C b (sum of base cations), Si, NO 3 − , and SO 4 2− , DOC and pH. Analyses of the relationships between Si, DOC, discharge and water table height clearly indicated that there was a decrease in ground water contributions (i.e., lower Si concentrations and higher DOC concentrations) as the watershed wetness increased with storm succession. The marked changes in chemistry were also reflected in changes in the isotopic composition of SO 4 2− and NO 3 − . There was a strong inverse relationship between SO 4 2− concentrations and δ 34 S values suggesting the importance of S biogeochemical redox processes in contributing to SO 4 2− export. The isotopic composition of NO 3 − in stream water indicated that this N had been microbially processed. Linkages between SO 4 2− and DOC concentrations suggest that wetlands were major sources of these solutes to drainage waters while the chemical and isotopic response of NO 3 − suggested that upland sources were more important. Although these late summer and fall storms did not play a major role in the overall annual mass balances of solutes for this watershed, these events had distinctive chemistry including depressed pH and therefore have important consequences to watershed processes such as episodic acidification, and the linkage of these processes to climate change.

Biogeochemistry↗

USGS2020

Phosphorus, nitrogen and dissolved organic carbon fluxes from sediments in freshwater rivermouths entering Green Bay (Lake Michigan; USA)

Transitional areas between ecosystem types are often active biogeochemically due to resource limitation changes. Lotic-to-lentic transitions in freshwaters appear active biogeochemically, but few studies have directly measured nutrient processing rates to assess whether processing within the rivermouth is important for load estimates or the local communities. We measured oxic fluxes of inorganic nitrogen and phosphorus and dissolved organic carbon (DOC) from sediments in two rivermouths of Green Bay (Lake Michigan, USA). Soluble reactive phosphorus (SRP) flux was positive in most cases (overall mean 1.74 mg SRP m − 2 day − 1 ), as was ammonium (NH 4 ) flux (40.6 mg NH 4 m − 2 day − 1 ). Partial least square regression (PLSR) indicated a latent variable associated with both sediment [loosely bound phosphorus (P), iron bound P, organic content] and water column properties [temperature, DOC:dissolved inorganic nitrogen (DIN) and DOC:SRP ratios (negatively)] that was moderately associated with variation in SRP flux. PLSR analysis also indicated several sediment characteristics were moderately related to NH 4 flux, especially organic content, density (negative), and porosity. Flux of nitrates/nitrites (NO X ) and DOC were positively associated with the water column concentrations of NO X and DOC and qualitative estimates of the labile, non-humic types of DOC. In early summer, water column NO X and DOC concentrations were high and labile DOC may have fueled denitrification, resulting in net flux into sediments of both NO X and DOC. By late summer, water column NO X and DOC were very low and both these constituents were fluxing out of sediments into the water column. Based on our estimates for the entire period from April through September, rivermouth sediments were a net source of SRP and DIN, with a DIN:SRP ratio of ~ 44 and a NH 4 :NO X > 1. We estimated that the sediments in the Fox rivermouth probably contributed a small proportion of the total Fox River load during the growing season 2016 (< 5%), but at times may have contributed as much as 14% of the daily load. Despite the small size of the Fox rivermouth (< 0.5% of the watershed area), these results indicate that at times sediments can contribute substantially to the overall delivery of nitrogen and phosphorus to the nearshore zone.

Wisconsin↗

USGS2017

Piscivore diet response to a collapse in pelagic prey populations

Pelagic fish populations in the upper San Francisco Estuary have experienced significant declines since the turn of the century; a pattern known as the pelagic organism decline (POD). This study investigated food habits of piscivorous fishes over two consecutive fall seasons following the decline of pelagic fish prey. Specifically, this study addressed the contribution of pelagic versus benthic prey to piscivorous fish diets, including the frequency of predation on special-status pelagic species, and the spatial variability in prey consumption. The piscivore community was dominated by Striped Bass and also included small numbers of Sacramento Pikeminnow and Largemouth Bass. Overall, pelagic prey items contributed less than 10% of the diet by weight in both years, whereas pre-POD studies gleaned from the literature found contributions of 39–100%, suggesting a major switch from pelagic to benthic prey resources. Between-year variation in piscivore diets reflected differences in environmental conditions associated with variation in freshwater outflow. No special status fish species were detected in any of the piscivore stomachs examined. The consequences of this pelagic to benthic diet shift warrants further investigation to understand its ecological relevance.

California↗

USGS2005

Combined use of rapid bioassessment protocols and sediment quality triad to assess stream quality

Physical, chemical and biological conditions at five stations on a small southeastern stream were evaluated using the Rapid Bioassessment Protocols (RBP) and the Sediment Quality Triad (SQT) to assess potential biological impacts of a municipal wastewater treatment facility (WWTF) on downstream resources. Physical habitat, benthic macroinvertebrates and fish assemblages were impaired at Stations 1 and 2 (upstream of the WWTF), suggesting that the degraded physical habitat was adversely impacting the fish and benthic populations. The SQT also demonstrated that Stations 1 and 2 were degraded, but the factors responsible for the impaired conditions were attributed to the elevated concentrations of polycylclic aromatic hydrocarbons (PAHs) and metals (Mn, Pb) in the sediments. The source of contaminants to the upper reaches of the stream appears to be storm-water runoff from the city center. Increased discharge and stabilized base flow contributed by the WWTF appeared to benefit the physically-altered stream system. Although the two assessment procedures demonstrated biological impairment at the upstream stations, the environmental factors identified as being responsible for the impairment were different: the RBP provided insight into contributions associated with the physical habitat and the SQT contributed information on contaminants and sediment quality. Both procedures are important in the identification of physical and chemical factors responsible for environmental impairment and together they provide information critical to the development of appropriate management options for mitigation.

Environmental Monitoring and Assessment↗

USGS2012

Reconstruction of past methane availability in an Arctic Alaska wetland indicates climate influenced methane release during the past ~12,000 years

Atmospheric contributions of methane from Arctic wetlands during the Holocene are dynamic and linked to climate oscillations. However, long-term records linking climate variability to methane availability in Arctic wetlands are lacking. We present a multi-proxy ~12,000 year paleoecological reconstruction of intermittent methane availability from a radiocarbon-dated sediment core (LQ-West) taken from a shallow tundra lake (Qalluuraq Lake) in Arctic Alaska. Specifically, stable carbon isotopic values of photosynthetic biomarkers and methane are utilized to estimate the proportional contribution of methane-derived carbon to lake-sediment-preserved benthic (chironomids) and pelagic (cladocerans) components over the last ~12,000 years. These results were compared to temperature, hydrologic, and habitat reconstructions from the same site using chironomid assemblage data, oxygen isotopes of chironomid head capsules, and radiocarbon ages of plant macrofossils. Cladoceran ephippia from ~4,000 cal year BP sediments have δ13C values that range from ~−39 to −31‰, suggesting peak methane carbon assimilation at that time. These low δ13C values coincide with an apparent decrease in effective moisture and development of a wetland that included Sphagnum subsecundum. Incorporation of methane-derived carbon by chironomids and cladocerans decreased from ~2,500 to 1,500 cal year BP, coinciding with a temperature decrease. Live-collected chironomids with a radiocarbon age of 1,640 cal year BP, and fossil chironomids from 1,500 cal year BP in the core illustrate that ‘old’ carbon has also contributed to the development of the aquatic ecosystem since ~1,500 cal year BP. The relatively low δ13C values of aquatic invertebrates (as low as −40.5‰) provide evidence of methane incorporation by lake invertebrates, and suggest intermittent climate-linked methane release from the lake throughout the Holocene.

Alaska↗

USGS2018

Fire changes the spatial distribution and sources of soil organic carbon in a grassland-shrubland transition zone

Aims In many mixed grass-shrub ecosystems, increased shrub biomass tends to promote overall carbon storage, but the distribution of carbon pools may be complicated by disturbances such as wildfires. We investigated the spatial distribution of surface soil organic carbon (SOC) and its relative contribution from grasses and shrubs after fires in a grass-shrub transition zone in the northern Chihuahuan Desert, USA. Methods We used a prescribed fire to create a burned treatment, then collected soil and plant samples. The biogeochemical approaches, geostatistical analyses, and carbon partitioning analyses were used to quantify the SOC and soil δ 13 C spatial patterns. Results Before the prescribed fire, up to 98% of the spatial dependence of SOC was autocorrelated at a distance of 1.91 m, corresponding to the approximate average shrub canopy diameter, but the spatial dependence dropped to 81% at a larger autocorrelation distance (3.74 m) two windy seasons after the fire. C 4 grasses and C 3 shrubs contributed approximately equal amounts of carbon to the surface SOC pool before the prescribed fire. However, C 4 grasses became the dominant source of SOC two windy seasons following the fire. For individual microsites, a substantially increased proportion of SOC was derived from C 4 grasses at the shrub microsites following the fire. Conclusions The higher proportion of C 4 grasses-derived SOC at the shrub microsites post-fire suggests that SOC may have preferred pathways to move among different microsites following fire disturbance. The distinct spatial distribution patterns of δ 13 C, and the increased contribution of SOC from grasses may be explained by the rapid recovery of grasses following the fire. Overall, our results provide insights into how fire might be used as a management tool to alter soil carbon pools in the context of shrub encroachment.

Plant and Soil↗

USGS2008

A mass balance mercury budget for a mine-dominated lake: Clear Lake, California

The Sulphur Bank Mercury Mine (SBMM), active intermittently from 1873–1957 and now a USEPA Superfund site, was previously estimated to have contributed at least 100 metric tons (10 5 kg) of mercury (Hg) into the Clear Lake aquatic ecosystem. We have confirmed this minimum estimate. To better quantify the contribution of the mine in relation to other sources of Hg loading into Clear Lake and provide data that might help reduce that loading, we analyzed Inputs and Outputs of Hg to Clear Lake and Storage of Hg in lakebed sediments using a mass balance approach. We evaluated Inputs from (1) wet and dry atmospheric deposition from both global/regional and local sources, (2) watershed tributaries, (3) groundwater inflows, (4) lakebed springs and (5) the mine. Outputs were quantified from (1) efflux (volatilization) of Hg from the lake surface to the atmosphere, (2) municipal and agricultural water diversions, (3) losses from out-flowing drainage of Cache Creek that feeds into the California Central Valley and (4) biotic Hg removal by humans and wildlife. Storage estimates include (1) sediment burial from historic and prehistoric periods (over the past 150–3,000 years) from sediment cores to ca. 2.5m depth dated using dichloro diphenyl dichloroethane (DDD), 210 Pb and 14 C and (2) recent Hg deposition in surficial sediments. Surficial sediments collected in October 2003 (11 years after mine site remediation) indicate no reduction (but a possible increase) in sediment Hg concentrations over that time and suggest that remediation has not significantly reduced overall Hg loading to the lake. Currently, the mine is believed to contribute ca. 322–331 kg of Hg annually to Clear Lake, which represents ca. 86–99% of the total Hg loading to the lake. We estimate that natural sedimentation would cover the existing contaminated sediments within ca. 150–300 years.

Water, Air, & Soil Pollution↗

USGS2016

From "Duck Factory" to "Fish Factory": Climate induced changes in vertebrate communities of prairie pothole wetlands and small lakes

The Prairie Pothole Region’s myriad wetlands and small lakes contribute to its stature as the “duck factory” of North America. The fishless nature of the region’s aquatic habitats, a result of frequent drying, freezing, and high salinity, influences its importance to waterfowl. Recent precipitation increases have resulted in higher water levels and wetland/lake freshening. In 2012–13, we sampled chemical characteristics and vertebrates (fish and salamanders) of 162 Prairie Pothole wetlands and small lakes. We used non-metric multidimensional scaling, principal component analysis, and bootstrapping techniques to reveal relationships. We found fish present in a majority of sites (84 %). Fish responses to water chemistry varied by species. Fathead minnows ( Pimephales promelas ) and brook sticklebacks ( Culaea inconstans ) occurred across the broadest range of conditions. Yellow perch ( Perca flavescens ) occurred in a smaller, chemically defined, subset. Iowa darters ( Etheostoma exile ) were restricted to the narrowest range of conditions. Tiger salamanders ( Ambystoma mavortium ) rarely occurred in lakes with fish. We also compared our chemical data to similar data collected in 1966–1976 to explore factors contributing to the expansion of fish into previously fishless sites. Our work contributes to a better understanding of relationships between aquatic biota and climate-induced changes in this ecologically important area.

North Dakota↗

USGS1962

The solubility of quartz in water in the temperature interval from 25° to 300° C

The solubility of quartz in water was investigated by three sets of experiments at 1000 atm P H 2 O and temperatures ranging from 45° to 300°C at water pressures appropriate for the coexistence of three phases, gaseous water, liquid, and quartz, at temperatures ranging from 69° to 240°C a long term study of the dissolution of quartz grains which were continuously tumbled in water at room temperature. Saturated silica solutions in equilibrium with quartz were obtained in a few days at temperatures above 100°C. Equilibrium is shown by reproducible results for runs of different durations and by the precipitation of quartz from initially supersaturated solutions. The differential heat of solution derived from the data obtained at 1000 atm pressure is 5.38 kcal/mole. At room temperature and pressure, highly supersaturated silica solutions were obtained by continuously rotating quartz grains and water in plastic bottles at 75 rev/min. In one run the amount of silica in solution increased to a maximum value of 395 p.p.m. after 370 days. Another run reached 80 p.p.m. silica after 386 days and then dropped to 6 p.p.m. silica. It is concluded that quartz was precipitated at room temperature from this supersaturated solution and that 6 p.p.m. is essentially the true solubility of quartz at 25°C. In contrast to the runs rotated at 75 rev/min, quartz grains, and also silica glass grains, continuously rotated in water at rev/min, each contributed less than 1 p.p.m. colorimetric silica into solution after 1 year. Thus, vigorous agitation of the liquid is necessary to remove dissolved silica from the vicinity of surfaces of both quartz and glass. Two significant factors that may have contributed to the formation of supersaturated silica solutions in the runs rotated at 75 rev/min at room temperature are stresses and structural irregularities at the surfaces of the crushed quartz grains, which contributed silica into solution more readily than well crystallized quartz the very slow rate at which dissolved silica polymerizes to species appropriate to act as nuclei for quartz growth. At the termination of the runs rotated at 75 rev/min, spikelike projections were present on many of the quartz grains. These are interpreted as indicating that abrasion was not the dominant cause for the great supersaturations which were obtained.

Geochimica et Cosmochimica Acta↗

USGS1964

Minor-element composition and organic carbon content of marine and nonmarine shales of Late Cretaceous age in the western interior of the United States

The composition of nonmarine shales of Cretaceous age that contain less than 1 per cent organic carbon is assumed to represent the inherited minor-element composition of clayey sediments delivered to the Cretaceous sea that occupied the western interior region of North America. Differences in minor-element content between these samples and samples of 1. (a) nonmarine carbonaceous shales (1 to 17 per cent organic carbon), 2. (b) nearshore marine shales (less than 1 per cent organic carbon), and 3. (c) offshore marine shales (as much as 8 per cent organic carbon), all of the same age, reveal certain aspects of the role played by clay minerals and organic materials in affecting the minor-element composition of the rocks. The organic carbon in the nonmarine rocks occurs in disseminated coaly plant remains. The organic carbon in the marine rocks occurs predominantly in humic material derived from terrestrial plants. The close similarity in composition between the organic isolates from the marine samples and low-rank coal suggests that the amount of marine organic material in these rocks is small. The minor-element content of the two kinds of nonmarine shales is the same despite the relatively large amount of organic carbon in the carbonaceous shales. The nearshore marine shales, however, contain larger median amounts of arsenic, boron, chromium, vanadium and zinc than do the nonmarine rocks; and the offshore marine shales contain even larger amounts of these elements. Cobalt, molybdenum, lead and zirconium show insignificant differences in median content between the nonmarine and marine rocks, although as much as 25 ppm molybdenum is present in some offshore marine samples. The gallium content is lower in the marine than in the nonmarine samples. Copper and selenium contents of the two kinds of nonmarine rocks and the nearshore marine samples are the same, but those of the offshore samples are larger. In general, arsenic, chromium, copper, molybdenum, selenium, vanadium and zinc are concentrated in those offshore marine samples having the largest amounts of organic carbon, but samples with equal amounts of vanadium, for instance, may differ by a factor of 3 in their amount of organic carbon. Arsenic and molybdenum occur in some samples chiefly in syngenetic pyrite but also are present in relatively large amounts in samples that contain little pyrite. The data on nonmarine carbonaceous shales indicate that organic matter of terrestrial origin in marine shales contributes little to the minor-element content of such rocks. It is possible that marine organic matter, even though seemingly small in amount in marine shales, contributes to the minor-element composition of the shales. In addition to any such contribution, however, the great effectiveness in sorption processes of humic materials in conjunction with clay minerals suggests that such processes must have played an important role as these materials moved from the relatively dilute solutions of the nonmarine environment to the relatively concentrated solution of sea water. The volumes of sea water sufficient to supply for sorption the amounts of most minor elements in the offshore marine samples are insignificant compared to the volumes of water with which the clay and organic matter were in contact during their transportation and sedimentation. Consequently, the chemical characteristics of the environment in which the clay minerals and organic matter accumulated and underwent diagenesis probably were the most important factors in controlling the degree to which sorption processes and the formation of syngenetic minerals affected the final composition of the rocks.

Geochimica et Cosmochimica Acta↗

USGS1992

The dynamic relationship between ground water and the Columbia River: Using deuterium and oxygen-18 as tracers

Deuterium and oxygen-18 were used as natural tracers to investigate the hydraulic relationship between the Columbia River and the Blue Lake gravel aquifer near Portland, Oregon. A time series of stable-isotope data collected from surface and ground waters during a March 1990 aquifer test confirms that the river and aquifer are hydraulically connected. Calculations based on simple mixing show that the river contributed 40–50% of the yield of three wells after 5–6 days of pumping. Data collected during August 1990, show that the river contributed 65–80% of the yield of one well after 22 days of pumping and indicate that the contribution of the river was still increasing.

Journal of Hydrology↗

USGS1991

Modes of cross-shore sediment transport on the shoreface of the Middle Atlantic Bight

The mechanisms responsible for onshore and offshore sediment fluxes across the shoreface zone seaward of the surf zone were examined in a 3-year field study. The study was conducted in the southern part of the Middle Atlantic Bight in the depth region 7–17 m using instrumented tripods supporting electromagnetic current meters, pressure sensors, suspended sediment concentration sensors, and sonar altimeters. The observations embraced fairweather, moderate energy, swell-dominated, and storm conditions. Cross-shore mean flows ranged from near zero during fairweather to > 20 cm s −1 during the storm; oscillatory flows were on the order of 10 cm s −1 during fairweather and 100 cm s −1 during the storm. Suspended sediment concentrations at about 10 cm above the bed were < 0.1 kg m −3 under fairweather conditions, 1–2 kg m −3 under moderate swell conditions, and > 5 kg m −3 during the storm. Three methods were applied to evaluate the relative importance of incident waves, long-period oscillations, mean flows and gravity in effecting shoreward or seaward sediment flux: (1) an energetics transport model was applied to instantaneous near-bottom velocity data, (2) higher moments of near-bottom flows were estimated and compared, and (3) suspended sediment fluxes were estimated directly from the instantaneous products of cross-shore velocity and suspended sediment concentration. The results show that measurable contributions were made by all four of the processes. Most significantly, mean flows were seen to dominate and cause offshore fluxes during the storm and to contribute significantly to onshore and offshore flux during fairweather and moderate energy. Incident waves were, in all cases, the major source of bed shear stress but also caused shoreward as well as seaward net sediment advection. Low-frequency effects involving wave groups and long-period waves made secondary contributions to cross-shore sediment flux. Contrary to expectations, low-frequency fluxes were just as often shoreward as seaward. Whereas cross-correlations between suspended sediment concentration and the instantaneous near-bottom current speed were high and in phase under storm conditions, they were weak and out of phase during fairweather conditions. This suggests that simple energetics models are probably inadequate for predicting fairweather transport of suspended sediment.

Middle Atlantic Bight↗

USGS1991

Large-scale distribution of metal contamination in the fine-grained sediments of the Clark Fork River, Montana, U.S.A.

Historic discharges from the mining and smelting complex at the head-waters of the Clark Fork River have resulted in elevated Ag, Cd, Cu, Pb and Zn concentrations in the <60 μm fraction of both bed and flood-plain sediments of the river. Processes affecting the trends in longitudinal distributions of these metals were investigated by repeated sampling over a 380 km river reach between August 1986 and July 1989. At the most upstream site, bed-sediment metal concentrations were enriched 18–115 times above least enriched tributaries, depending on the metal. All metals decreased exponentially with distance downstream away from mining. The exponential model predicts that elevated metal concentrations should occur over 550 km downstream, in Lake Pend Oreille. Longitudinal trends, obvious on a scale of hundreds of kilometers, were obscured by small-scale spatial variability when shorter stretches of the river were considered. Longitudinal dispersion appeared to be controlled largely by physical dilution with less-contaminated sediments. Evidence suggests that erosion of contaminated flood-plains contributes to metal contamination in the bed sediments. Tributary input appeared to have little influence on the large-scale, downstream distribution of metals; however, it did contribute to local variability in bed-sediment metal concentrations. Association of metals with specific mineral grains, as well as variability in total organic C and Fe concentration, appeared also to contribute to variability. Some year-to-year variability in bed-sediment metal concentrations was observed, however, trends in longitudinal dispersion were not significantly different between at least two of the years sampled.

Montana↗

USGS2019

Reproductive failure in the Eastern Migratory Population: The interaction of research and management

The reintroduction of the Eastern Migratory Population of Whooping Cranes ( Grus americana ) has shown the most promise of any effort to date toward the establishment of a self-sustaining population. However, reproduction – including both nest success and chick survival – has been a major challenge. Here, we review the research and management efforts deployed to identify and address this challenge. While there is evidence that a proximal cause of nest failure is harassment by blood-feeding black flies ( Simulium spp. ), this is not likely to be the only contributing factor, and we present alternative hypotheses. There is less understanding of the causes of poor chick survival, and we present hypotheses for factors that may be contributing to chick mortality, including environmental, genetic, and behavioral factors. For both nest success and chick survival, we carried out a value of information analysis, using expert judgment, which allowed us to prioritize the alternative hypotheses for evaluation based on the expected management benefit of addressing each hypothesis. On the horizon are multiple opportunities to explore hypotheses about environmental factors as well as genetic and behavioral characteristics of the birds themselves that may contribute to poor reproduction. If bird-specific characteristics, such as genetics or rearing methods, are hindering reproduction, this has important implications for all efforts to restore Whooping Crane populations.

Book chapter↗

USGS2024

Characterizing variability in geochemistry and mineralogy of western US dust sources

Dust events originate from multiple sources in arid and semi-arid regions, making it difficult to quantify source contributions. Dust geochemical/mineralogical composition, if the sources are sufficiently distinct, can be used to quantify the contributions from different sources. To test the viability of using geochemical and mineralogical measurements to separate dust-emitting sites, we used dust samples collected between 2018 and 2020 from ten National Wind Erosion Research Network (NWERN) sites that are representative of western United States (US) dust sources. Dust composition varied seasonally at many of the sites, but within-site variability was smaller than across-site variability, indicating that the geochemical signatures are robust over time. It was not possible to separate all the sites using commonly applied principal component analysis (PCA) and cluster analysis because of overlap in dust geochemistry. However, a linear discriminant analysis (LDA) successfully separated all sites based on their geochemistry, suggesting that LDA may prove useful for separating dust sources that cannot be separated using PCA or other methods. Further, an LDA based on mineralogical data separated most sites using only a limited number of mineral phases that were readily explained by the local geologic setting. Taken together, the geochemical and mineralogical measurements generated distinct signatures of dust emissions across NWERN sites. If expanded to include a broader range of sites across the western US, a library of geochemical and mineralogical data may serve as a basis to track and quantify dust contributions from these sources.

Aeolian Research↗

USGS2005

Relation of baseflow to row crop intensity in Iowa

Increasing baseflow and baseflow percentage over the second half of the 20th century in Iowa has contributed to increasing nitrate-nitrogen concentrations measured in Iowa rivers because nitrate is primarily delivered to streams as baseflow and tile drainage. The relation of baseflow and baseflow percentage to row crop land use was evaluated for 11 Iowa rivers and their watersheds for their period of streamflow record (58-73 years period). Results indicated increasing baseflow in Iowa's rivers is significantly related to increasing row crop intensity. A 13-52% increase in row crop percentage in many Iowa watersheds has contributed to an increase of 33-135 mm increase in baseflow and 7-31% increase in baseflow percentage. Limited historical water quality data from two larger Iowa rivers (Cedar and Raccoon rivers) suggest that increasing row crop land use over the 20th century has produced more baseflow and contributed to increasing nitrate concentrations in Iowa's rivers. ?? 2004 Elsevier B.V. All rights reserved.

Agriculture, Ecosystems and Environment↗

USGS2014

Approximations of stand water use versus evapotranspiration from three mangrove forests in southwest Florida, USA

Leaves from mangrove forests are often considered efficient in the use of water during photosynthesis, but less is known about whole-tree and stand-level water use strategies. Are mangrove forests as conservative in water use as experimental studies on seedlings imply? Here, we apply a simple model to estimate stand water use ( S ), determine the contribution of S to evapotranspiration (ET), and approximate the distribution of S versus ET over annual cycles for three mangrove forests in southwest Florida, USA. The value of S ranged from 350 to 511 mm year −1 for two mangrove forests in Rookery Bay to 872 mm year −1 for a mangrove forest along the Shark River in Everglades National Park. This represents 34–49% of ET for Rookery Bay mangroves, a rather conservative rate of S , and 63–66% of ET for the Shark River mangroves, a less conservative rate of S . However, variability in estimates of S in mangroves is high enough to require additional study on the spatial changes related to forest structural shifts, different tidal regimes, and variable site-specific salinity concentrations in multiple mangrove forests before a true account of water use conservation strategies can be understood at the landscape scale. Evidence does suggest that large, well-developed mangrove forests have the potential to contribute considerably to the ET balance; however, regionally most mangrove forests are much smaller in stature in Florida and likely contribute less to regional water losses through stand-level transpiration.

Florida↗

USGS2010

Identifying sources of stream water sulfate after a summer drought in the Sleepers River watershed (Vermont, USA) using hydrological, chemical, and isotopic techniques

In many forested headwater catchments, peak SO 4 2 - concentrations in stream water occur in the late summer or fall following drought potentially resulting in episodic stream acidification. The sources of highly elevated stream water SO 4 2 - concentrations were investigated in a first order stream at the Sleepers River watershed (Vermont, USA) after the particularly dry summer of 2001 using a combination of hydrological, chemical and isotopic approaches. Throughout the summer of 2001 SO 4 2 - concentrations in stream water doubled from ???130 to 270 ??eq/L while flows decreased. Simultaneously increasing Na + and Ca 2+ concentrations and ?? 34 S values increasing from +7??? towards those of bedrock S (???+10.5???) indicated that chemical weathering involving hydrolysis of silicates and oxidation of sulfide minerals in schists and phyllites was the cause for the initial increase in SO 4 2 - concentrations. During re-wetting of the watershed in late September and early October of 2001, increasing stream flows were accompanied by decreasing Na + and Ca 2+ concentrations, but SO 4 2 - concentrations continued to increase up to 568 ??eq/L, indicating that a major source of SO 4 2 - in addition to bedrock weathering contributed to peak SO 4 2 - concentrations. The further increase in SO 4 2 - concentrations coincided with an abrupt decrease of ?? 34 S values in stream water SO 4 2 - from maximum values near +10??? to minimum values near -3???. Soil investigations revealed that some C-horizons in the Spodsols of the watershed contained secondary sulfide minerals with ?? 34 S values near -22???. The shift to negative ?? 34 S values of stream water SO 4 2 - indicates that secondary sulfides in C-horizons were oxidized to SO 4 2 - during the particularly dry summer of 2001. The newly formed SO 4 2 - was transported to the streams during re-wetting of the watershed contributing ???60% of the SO 4 2 - during peak concentrations in the stream water. Thereafter, the contribution of SO 4 2 - from oxidation of secondary sulfides in C-horizons decreased rapidly and pedogenic SO 4 2 - reemerged as a dominant SO 4 2 - source in concert with decreasing SO 4 2 - concentrations in spring of 2002. The study provides evidence that a quantitative assessment of the sources of stream water SO 4 2 - in forested watersheds is possible by combining hydrological, chemical and isotopic techniques, provided that the isotopic compositions of all potential SO 4 2 - sources are distinctly different. ?? 2010 Elsevier Ltd.

Applied Geochemistry↗