SEARCH · USGS Science

Results for “Chemistry”

Search indexed USGS publications on groundwater, aquifers, geologic maps, mineral resources and earthquakes. Explore source records by subject and place.

SourceResearch connectionFrom yearThrough year

Quote a phrase for an exact phrase match. Source license links do not imply unrestricted reuse.

At least 865 records · Page 48Linked to original sources

USGS2008

Discrimination of lichen genera and species using element concentrations

The importance of organic chemistry in the classification of lichens is well established, but inorganic chemistry has been largely overlooked. Six lichen species were studied over a period of 23 years that were growing in 11 protected areas of the northern Great Lakes ecoregion, which were not greatly influenced by anthropogenic particulates or gaseous air pollutants. The elemental data from these studies were aggregated in order to test the hypothesis that differences among species in tissue element concentrations were large enough to discriminate between taxa faithfully. Concentrations of 16 chemical elements that were found in tissue samples from Cladonia rangiferina, Evernia mesomorpha, Flavopunctelia flaventior, Hypogymnia physodes, Parmelia sulcata, and Punctelia rudecta were analyzed statistically using multivariate discriminant functions and CART analyses, as well as t-tests. Genera and species were clearly separated in element space, and elemental discriminant functions were able to classify 91-100 of the samples correctly into species. At the broadest level, a Zn concentration of 51 ppm in tissues of four of the lichen species effectively discriminated foliose from fruticose species. Similarly, a S concentration of 680 ppm discriminated C. rangiferina and E. mesomorpha , and a Ca concentration of 10 436 ppm discriminated H. physodes from P. sulcata . For the three parmelioid species, a Ca concentration >32 837 ppm discriminated Punctelia rudecta from the other two species, while a Zn concentration of 56 ppm discriminated Parmelia sulcata from F. flaventior . Foliose species also had higher concentrations than did fruticose species of all elements except Na. Elemental signatures for each of the six species were developed using standardized means. Twenty-four mechanisms explaining the differences among species are summarized. Finally, the relationships of four species based on element concentrations, using additive-trees clustering of a Euclidean-distance matrix, produced identical relationships as did analyses based on secondary product chemistry that used additive-trees clustering of a Jaccard similarity matrix. At least for these six species, element composition has taxonomic significance, and may be useful for discriminating other taxa.

Great Lakes↗

USGS1999

Inhibition of hydroxyl radical reaction with aromatics by dissolved natural organic matter

Reaction of aromatic compounds with hydroxyl radical is inhibited by dissolved natural organic matter (NOM). The degree of inhibition is significantly greater than that expected based on a simple model in which aromatic compound molecules bound to NOM are considered to be unreactive. In this study, hydroxyl radical was produced at steady-state concentrations using Fenton chemistry (H2O2 + Fe2+ ??? Fe3+ + HO- + HO??). Suwannee River fulvic acid and humic acid were used as NOM. The most likely mechanism for the observed inhibition is that hydroxyl radical formation occurs in microenvironmental sites remote from the aromatic compounds. In addition to changes in kinetics, pyrene hydroxyl radical reaction also exhibited a mechanistic change in the presence of fulvic acid. The mechanism changed from a reaction that was apparently firstorder in pyrene to one that was apparently secondorder in pyrene, indicating that pyrene self-reaction may have become the dominant mechanism in the presence of fulvic acid. Dissolved NOM causes significant changes in the rate and mechanism of hydroxyl radical degradation of aromatic compounds. Consequently, literature rate constants measured in pure water will not be useful for predicting the degradation of pollutants in environmental systems. The kinetic and mechanistic information in this study will be useful for developing improved degradation methods involving Fenton chemistry.Reaction of aromatic compounds with hydroxyl radical is inhibited by dissolved natural organic matter (NOM). The degree of inhibition is significantly greater than that expected based on a simple model in which aromatic compounds molecules bounds to NOM are considered to be unreactive. In this study, hydroxyl radical was produced at steady-state concentrations using Fenton chemistry (H2O2 + Fe2+ ??? Fe3+ + HO- + HO??). Suwannee River fulvic acid and humic acid were used as NOM. The most likely mechanisms for the observed inhibition is that hydroxyl radical formation occurs in microenvironmental sites remote from the aromatic compounds. In addition to changes in kinetics, pyrene hydroxyl radical reaction also exhibited a mechanistic change in the presence of fulvic acid. The mechanism changed from a reaction that was apparently first-order in pyrene to one that was apparently second-order in pyrene, indicating that pyrene self-reaction may have become the dominant mechanism in the presence of fulvic acid. Dissolved NOM causes significant changes in the rate and mechanism of hydroxyl radical degradation of aromatic compounds. Consequently, literature rate constants measured in pure water will not be useful for predicting the degradation of pollutants in environmental systems. The kinetic and mechanistic information in this study will be useful for developing improved degradation methods involving Fenton chemistry.

Environmental Science & Technology↗

USGS2020

The GFDL Earth System Model Version 4.1 (GFDL-ESM 4.1): Overall coupled model description and simulation characteristics

We describe the baseline coupled model configuration and simulation characteristics of GFDL's Earth System Model Version 4.1 (ESM4.1), which builds on component and coupled model developments at GFDL over 2013–2018 for coupled carbon-chemistry-climate simulation contributing to the sixth phase of the Coupled Model Intercomparison Project. In contrast with GFDL's CM4.0 development effort that focuses on ocean resolution for physical climate, ESM4.1 focuses on comprehensiveness of Earth system interactions. ESM4.1 features doubled horizontal resolution of both atmosphere (2° to 1°) and ocean (1° to 0.5°) relative to GFDL's previous-generation coupled ESM2-carbon and CM3-chemistry models. ESM4.1 brings together key representational advances in CM4.0 dynamics and physics along with those in aerosols and their precursor emissions, land ecosystem vegetation and canopy competition, and multiday fire; ocean ecological and biogeochemical interactions, comprehensive land-atmosphere-ocean cycling of CO 2 , dust and iron, and interactive ocean-atmosphere nitrogen cycling are described in detail across this volume of JAMES and presented here in terms of the overall coupling and resulting fidelity. ESM4.1 provides much improved fidelity in CO 2 and chemistry over ESM2 and CM3, captures most of CM4.0's baseline simulations characteristics, and notably improves on CM4.0 in (1) Southern Ocean mode and intermediate water ventilation, (2) Southern Ocean aerosols, and (3) reduced spurious ocean heat uptake. ESM4.1 has reduced transient and equilibrium climate sensitivity compared to CM4.0. Fidelity concerns include (1) moderate degradation in sea surface temperature biases, (2) degradation in aerosols in some regions, and (3) strong centennial scale climate modulation by Southern Ocean convection.

Journal of Advances in Modeling Earth Systems (JAM↗

USGS2010

Comparison of episodic acidification of Mid-Atlantic Upland and Coastal Plain streams

Episodic acidification was examined in five mid-Atlantic watersheds representing three physiographic provinces: Coastal Plain, Valley and Ridge, and Blue Ridge. Each of the watersheds receives a similar loading of atmospheric pollutants (SO 4 2− and NO 3 − ) and is underlain by different bedrock type. The purpose of this research was to quantify and compare the episodic variability in storm flow chemistry in Reedy Creek, Virginia (Coastal Plain), Mill Run and Shelter Run, Virginia (Valley and Ridge), and Fishing Creek Tributary and Hunting Creek, Maryland (Blue Ridge). Because episodic responses were similar from storm to storm in each of the watersheds, a representative storm from each watershed was discussed. Acidification, defined as the loss of acid-neutralizing capacity (ANC), was observed in all streams except Mill Run. Mill Run chemistry showed little episodic variability. During storms in the other streams, p H decreased while SO 4 2− , NO 3 − , and K + concentrations increased. Concentrations of Mg 2+ and Ca 2+ increased in Reedy Creek and Fishing Creek Tributary, but decreased in Shelter Run and Hunting Creek. Therefore the net effect of episodic changes on the acid-base status differed among the streams. In general, greater losses of ANC were observed during storms at Shelter Run and Hunting Creek, watersheds underlain by reactive bedrock (carbonate, metabasalt); comparatively smaller losses in ANC were observed at Reedy Creek and Fishing Creek Tributary, watersheds underlain by quartzites and unconsolidated quartz sands and cobbles. Increased SO 4 2− concentrations were most important during storms at Reedy Creek and Fishing Creek Tributary, but organic anions (inferred by anion deficit) were also a factor in causing the loss of ANC. Dilution of base cations was the most important factor in the loss of ANC at Shelter Run. Both increased sulfate and dilution of base flow were important in causing the episodic acidification at Hunting Creek. The role of SO 4 2− in contributing to episodic acidification in these watersheds is similar to that documented in studies conducted in other regions of the United States, Scandinavia, Canada, and the United Kingdom. The importance of SO 4 2− in mid-Atlantic United States streams contrasts with northeastern United States streams, in which increased NO 3 - derived from snowpack is more important in causing episodic acidification. Results support the importance of shallow subsurface processes in determining storm flow chemistry, regional climatic characteristics in determining the different sources of acidity during episodes, and the importance of bedrock geology in determining the amount of ANC loss.

Maryland, Virginia, West Virginia↗

USGS2010

Transport of reacting solutes in porous media: Relation between mathematical nature of problem formulation and chemical nature of reactions

Examples involving six broad reaction classes show that the nature of transport-affecting chemistry may have a profound effect on the mathematical character of solute transport problem formulation. Substantive mathematical diversity among such formulations is brought about principally by reaction properties that determine whether (1) the reaction can be regarded as being controlled by local chemical equilibria or whether it must be considered as being controlled by kinetics, (2) the reaction is homogeneous or heterogeneous, (3) the reaction is a surface reaction (adsorption, ion exchange) or one of the reactions of classical chemistry (e.g., precipitation, dissolution, oxidation, reduction, complex formation). These properties, as well as the choice of means to describe them, stipulate, for instance, (1) the type of chemical entities for which a formulation's basic, mass-balance equations should be written; (2) the nature of mathematical transformations needed to change the problem's basic equations into operational ones. These and other influences determine such mathematical features of problem formulations as the nature of the operational transport-equation system (e.g., whether it involves algebraic, partial-differential, or integro-partial-differential simultaneous equations), the type of nonlinearities of such a system, and the character of the boundaries (e.g., whether they are stationary or moving). Exploration of the reasons for the dependence of transport mathematics on transport chemistry suggests that many results of this dependence stem from the basic properties of the reactions' chemical-relation (i.e., equilibrium or rate) equations.

Water Resources Research↗

USGS2010

Geochemistry of groundwater in tertiary and cretaceous sediments of the southeastern Coastal Plain in eastern Georgia, South Carolina, and southeastern North Carolina

Geochemical samples of groundwater taken along hydrologic flow paths in eastern Georgia, South Carolina, and southeastern North Carolina, from noncalcareous sand aquifers, largely of Cretaceous age, are dominated by sodium and bicarbonate ions. Calcareous sand aquifers, largely of Tertiary age, contain water whose chemistry is dominated by calcium and bicarbonate ions, but may evolve downgradient to sodium and bicarbonate dominance. Water chemistry in both types of aquifer evolves to sodium chloride dominance as a result of fresh water mixing with subsurface brines or seawater present in the deeper downgradient parts of the aquifers. Principal aqueous chemical reactions appear to occur in five reaction zones in the aquifers and include feldspar hydrolysis to kaolinite, calcite dissolution, calcium-for-sodium cation exchange, and neoformation of sodium smectite in the downgradient parts of the aquifers. Redox reactions produce dissolved iron concentrations greater than 1 mg/L near the recharge areas. Organic matter in the aquifers is oxidized to CO 2 by iron reduction and sulfate reduction processes. Production of CO 2 by a methanogenic process may also occur. Geochemical mass-transfer models simulating the observed chemistry in western Alabama and eastern Mississippi have been extended to account for higher concentrations of sodium and bicarbonate observed in the South Carolina part of the aquifers.

Georgia, North Carolina, South Carolina↗

USGS2022

Sensitivity of headwater streamflow to thawing permafrost and vegetation change in a warming Arctic

Climate change has the potential to impact headwater streams in the Arctic by thawing permafrost and subsequently altering hydrologic regimes and vegetation distribution, physiognomy and productivity. Permafrost thaw and increased subsurface flow have been inferred from the chemistry of large rivers, but there is limited empirical evidence of the impacts to headwater streams. Here we demonstrate how changing vegetation cover and soil thaw may alter headwater catchment hydrology using water budgets, stream discharge trends, and chemistry across a gradient of ground temperature in northwestern Alaska. Colder, tundra-dominated catchments shed precipitation through stream discharge, whereas in warmer catchments with greater forest extent, evapotranspiration and infiltration are substantial fluxes. Forest soils thaw earlier, remain thawed longer, and display seasonal water content declines, consistent with greater evapotranspiration and infiltration. Streambed infiltration and water chemistry indicate that even minor warming can lead to increased infiltration and subsurface flow. Additional warming, permafrost loss, and vegetation shifts in the Arctic will deliver water back to the atmosphere and to subsurface aquifers in many regions, with the potential to substantially reduce discharge in headwater streams, if not compensated by increasing precipitation. Decreasing discharge in headwater streamflow will have important implications for aquatic and riparian ecosystems.

Alaska↗

USGS1996

Chemical evaluation of soil-solution in acid forest soils

Soil-solution chemistry is commonly studied in forests through the use of soil lysimeters.This approach is impractical for regional survey studies, however, because lysimeter installation and operation is expensive and time consuming. To address these problems, a new technique was developed to compare soil-solution chemistry among red spruce stands in New York, Vermont, New Hampshire, Maine. Soil solutions were expelled by positive air pressure from soil that had been placed in a sealed cylinder. Before the air pressure was applied, a solution chemically similar to throughfall was added to the soil to bring it to approximate field capacity. After the solution sample was expelled, the soil was removed from the cylinder and chemically analyzed. The method was tested with homogenized Oa and Bs horizon soils collected from a red spruce stand in the Adirondack Mountains of New York, a red spruce stand in east-central Vermont, and a mixed hardwood stand in the Catskill Mountains of New York. Reproducibility, effects of varying the reaction time between adding throughfall and expelling soil solution (5-65 minutes) and effects of varying the chemical composition of added throughfall, were evaluated. In general, results showed that (i) the method was reproducible (coefficients of variation were generally < 15%), (ii) variations in the length of reaction-time did not affect expelled solution concentrations, and (iii) adding and expelling solution did not cause detectable changes in soil exchange chemistry. Concentrations of expelled solutions varied with the concentrations of added throughfall; the lower the CEC, the more sensitive expelled solution concentrations were to the chemical concentrations of added throughfall. Addition of a tracer (NaBr) showed that the expelled solution was a mixture of added solution and solution that preexisted in the soil. Comparisons of expelled solution concentrations with concentrations of soil solutions collected by zero-tension and tension lysimetry indicated that expelled solution concentrations were higher than those obtained with either type of lysimeter, although there was less difference with tension lysimeters than zero-tension lysimeters. The method used for collection of soil solution should be taken into consideration whenever soil solution data are being interpreted.

New York, Vermont↗

USGS2004

Variation in responses to spawning Pacific salmon among three south-eastern Alaska streams

1. Pacific salmon are thought to stimulate the productivity of the fresh waters in which they spawn by fertilising them with marine-derived nutrients (MDN). We compared the influence of salmon spawners on surface streamwater chemistry and benthic biota among three southeastern Alaska streams. Within each stream, reaches up- and downstream of barriers to salmon migration were sampled during or soon after spawners entered the streams. 2. Within streams, concentrations of dissolved ammonium and soluble reactive phosphorus (SRP), abundance of epilithon (chlorophyll a and ash-free dry mass) and biomass of chironomids were significantly higher in reaches with salmon spawners. In contrast, biomass of the mayflies Epeorus spp. and Rhithrogena spp. was significantly higher in reaches lacking spawners. 3. Among streams, significant differences were found in concentrations of dissolved ammonium, dissolved organic carbon, nitrate and SRP, abundance of epilithon, and the biomass of chironomids and Rhithrogena. These differences did not appear to reflect differences among streams in spawner density, nor the changes in water chemistry resulting from salmon spawners. 4. Our results suggest that the 'enrichment' effect of salmon spawners (e.g. increased streamwater nutrient concentrations) was balanced by other concurrent effects of spawners on streams (e.g. sediment disturbance). Furthermore, the collective effect of spawners on lotic ecosystems is likely to be constrained by conditions unique to individual streams, such as temperature, background water chemistry and light attenuation.

Freshwater Biology↗

USGS2005

Geochemical variations in a core of hydrogeologic units near Freehold, New Jersey

Solutes were determined for 26 pore-water samples extracted from Tertiary and Cretaceous core material from a 1,320-foot-deep test borehole at Freehold, New Jersey. The cored materials are sediments that form a multilayered aquifer system of seven aquifers and eight confining units in the New Jersey Coastal Plain. The sediments are of marine origin in the upper 650 feet of the core and primarily nonmarine below 650 feet. Total concentrations of silica and major anions (SO 4 -2 and Cl - ) and cations (Ca +2 , Mg +2 , total Fe, Mn +2 , Na + , and K + ) in the pore-water samples varied with depth. Three core intervals are defined by water- chemistry variations, the environment of deposition (marine or nonmarine), and the degree of alteration (weathered or unweathered) of the units. Calcium, magnesium, sulfate, and total-ion concentrations were greater in the midcore (unweathered marine) interval than in the upper (weathered marine) and lower (fluviodeltaicsilicate) intervals of the core. Generally, pore-water chemical types in confining units were distinct from those found in aquifers–particularly in the midcore interval. In this interval, observed variations in pore-water chemistry in part reflect carbonate dissolution and cation exchange reactions common in Coastal Plain sediments. However, high concentrations of sulfate in unweathered marine sediments indicate novel processes may be important factors influencing pore-water chemistry in confining units.

Groundwater↗

USGS2005

Observed and simulated movement of bank-storage water

Detailed hydrologic and water-chemistry data were collected that document the movement of bank-storage water during March 7-April 17, 1990, in an alluvial aquifer adjacent to the Cedar River, Iowa. Hydrologic data included 745 daily ground-water-level measurements from 27 observation wells. Water-chemistry data indicate that bank-storage water had smaller specific conductance and larger concentration of atrazine than ambient ground water. To quantify the movement of the bank-storage water, a two-dimensional ground-water flow model was constructed, and the resulting calibrated model accurately simulated observed conditions. Analysis of water chemistry and model results indicate that a 2-meter rise in the river stage caused bank-storage water to move horizontally at least 30 meters into the aquifer and vertically about 4 meters below the river bottom, whereas the remaining 30 percent moved laterally through the riverbank. The model also showed that bank storage caused the ground-water flux to the river to increase by a factor of five during the first three weeks of base flow after runoff and that it required about five weeks for bank-storage water to discharge from the alluvial aquifer after the peak river stage. These results quantitatively demonstrate the importance of bank storage as a source of recharge to the alluvial aquifer and as a source of water to the river during early base-flow conditions.

Iowa↗

USGS2005

Geophysical monitoring of a field-scale biostimulation pilot project

The USGS conducted a geophysical investigation in support of a U.S. Naval Facilities Engineering Command, Southern Division field‐scale biostimulation pilot project at Anoka County Riverfront Park (ACP), downgradient of the Naval Industrial Reserve Ordnance Plant, Fridley, Minnesota. The goal of the pilot project is to evaluate subsurface injection of vegetable oil emulsion (VOE) to stimulate microbial degradation of chlorinated hydrocarbons. To monitor the emplacement and movement of the VOE and changes in water chemistry resulting from VOE dissolution and/or enhanced biological activity, the USGS acquired cross‐hole radar zero‐offset profiles, traveltime tomograms, and borehole geophysical logs during five site visits over 1.5 years. Analysis of pre‐ and postinjection data sets using petrophysical models developed to estimate VOE saturation and changes in total dissolved solids provides insights into the spatial and temporal distribution of VOE and ground water with altered chemistry. Radar slowness‐difference tomograms and zero‐offset slowness profiles indicate that the VOE remained close to the injection wells, whereas radar attenuation profiles and electromagnetic induction logs indicate that bulk electrical conductivity increased downgradient of the injection zone, diagnostic of changing water chemistry. Geophysical logs indicate that some screened intervals were located above or below zones of elevated dissolved solids; hence, the geophysical data provide a broader context for interpretation of water samples and evaluation of the biostimulation effort. Our results include (1) demonstration of field and data analysis methods for geophysical monitoring of VOE biostimulation and (2) site‐specific insights into the spatial and temporal distributions of VOE at the ACP.

Minnesota↗

USGS1973

Eclogites from southwestern Oregon

Eclogite, high-grade blueschist, and amphibolite blocks occur within the Mesozoic Otter Point Formation of southwestern Oregon and are inferred to have been tectonically emplaced by eastward-directed overthrusting involving Colebrooke Schist and serpentinite. Eclogite from southwestern Oregon is very similar in bulk chemistry and mineralogy to the well-studied eclogite of California. Calculations of phase equilibria at load pressures of 7 and 10 kb and T = 400°C to 550°C suggest that many of the hydrates found in eclogite could have been stable at very low H 2 O fugacities. The lack of lawsonite and the presence of almandine-grossular garnet set a maximum limit on H 2 O fugacity for a given P s -T. Chemically, Group C eclogite from Oregon and California characteristically is nepheline normative and is enriched in normative diopside relative to basaltic compositions. The present chemistry of this eclogite may be the result of metasomatism in an ultramafic environment with low a SiO 2 and high a Ca, but outside the stability field of serpentine. The generally high jadeite content of clinopyroxene from Group C eclogite compared with Group A and Group B eclogite is largely a function of bulk rock chemistry. Crystallization under low a SiO 2 conditions stabilizes jadeite in clinopyroxene at lower P s for a given T.

Oregon↗

USGS2026

Using sediment chemical fractions and multivariate statistics on water to identify sources, mobility, and bioavailability of aluminum in the Florida River near Durango, Colorado

The Florida River in southwestern Colorado, USA, flows through the Southern Ute Reservation and is a cultural and water resource to Tribal and non-Tribal communities. High concentrations of total Al, up to 16 400 µg l –1 , have been detected in the Florida River. Elevated Al concentrations in water may affect aquatic organisms’ ability to regulate ions and inhibit respiratory functions. Water chemistry collected during three sampling events in 2022 from the Florida River and two of its tributaries are used here to better understand the spatial distribution, seasonality, and sources of Al concentrations in the Florida River. Streambed sediment and rock chemistry is also used to infer geologic sources of Al in the watershed. A five-stage sequential extraction was performed on streambed sediment and rock samples to help determine Al transport processes. We assessed relations between major and trace elements in water using a principal component analysis, finding that high Al concentrations in the Florida River (>3500 µg l –1 total Al) are caused by the erosion of Al-laden sediments. We used a stepwise multiple linear regression to investigate the relationship between land use and Al concentrations. Land use did not reliably predict Al concentration, though increased streamflow connected to reservoir releases – particularly in the Salt Creek tributary – were found to contribute Al to the Florida River during the irrigation season. In this study, we demonstrate that successful metal source appropriation may be achieved through limited field sampling when performed with sufficient water chemistry analysis, sequential chemical extraction of stream sediments, and statistical and land-use analysis.

Colorado↗

USGS2016

Chemical and isotopic changes in Williston Basin brines during long-term oil production: An example from the Poplar dome, Montana

Brine samples were collected from 30 conventional oil wells producing mostly from the Charles Formation of the Madison Group in the East and Northwest Poplar oil fields on the Fort Peck Indian Reservation, Montana. Dissolved concentrations of major ions, trace metals, Sr isotopes, and stable isotopes (oxygen and hydrogen) were analyzed to compare with a brine contaminant that affected groundwater northeast of the town of Poplar. Two groups of brine compositions, designated group I and group II, are identified on the basis of chemistry and 87 Sr/ 86 Sr ratios. The solute chemistry and Sr isotopic composition of group I brines are consistent with long-term residency in Mississippian carbonate rocks, and brines similar to these contaminated the groundwater. Group II brines probably resided in clastic rocks younger than the Mississippian limestones before moving into the Poplar dome to replenish the long-term fluid extraction from the Charles Formation. Collapse of strata at the crest of the Poplar dome resulting from dissolution of Charles salt in the early Paleogene probably developed pathways for the ingress of group II brines from overlying clastic aquifers into the Charles reservoir. Such changes in brine chemistry associated with long-term oil production may be a widespread phenomenon in the Williston Basin.

Montana↗

USGS2024

Chemical and mineralogical characteristics of French green clays used for healing

The worldwide emergence of infectious diseases, together with the increasing incidence of antibiotic-resistant bacteria, elevate the need to properly detect, prevent, and effectively treat these infections. The overuse and misuse of common antibiotics in recent decades stimulates the need to identify new inhibitory agents. Therefore, natural products like clays, that display antibacterial properties, are of particular interest. The absorptive properties of clay minerals are well documented for healing skin and gastrointestinal ailments. However, the antibacterial properties of clays have received less scientific attention. French green clays have recently been shown to heal Buruli ulcer, a necrotic or ‘flesh-eating’ infection caused by Mycobacterium ulcerans . Assessing the antibacterial properties of these clays could provide an inexpensive treatment for Buruli ulcer and other skin infections. Antimicrobial testing of the two clays on a broad-spectrum of bacterial pathogens showed that one clay promotes bacterial growth (possibly provoking a response from the natural immune system), while another kills bacteria or significantly inhibits bacterial growth. This paper compares the mineralogy and chemical composition of the two French green clays used in the treatment of Buruli ulcer. Mineralogically, the two clays are dominated by 1 Md illite and Fe-smectite. Comparing the chemistry of the clay minerals and exchangeable ions, we conclude that the chemistry of the clay, and the surface properties that affect pH and oxidation state, control the chemistry of the water used to moisten the clay poultices and contribute the critical antibacterial agent(s) that ultimately debilitate the bacteria.

Clays and Clay Minerals↗

USGS2006

Upland disturbance affects headwater stream nutrients and suspended sediments during baseflow and stormflow

Because catchment characteristics determine sediment and nutrient inputs to streams, upland disturbance can affect stream chemistry. Catchments at the Fort Benning Military Installation (near Columbus, Georgia) experience a range of upland disturbance intensities due to spatial variability in the intensity of military training. We used this disturbance gradient to investigate the effects of upland soil and vegetation disturbance on stream chemistry. During baseflow, mean total suspended sediment (TSS) concentration and mean inorganic suspended sediment (ISS) concentration increased with catchment disturbance intensity (TSS: R2 = 0.7, p = 0.005, range = 4.0-10.1 mg L-1; ISS: R2 = 0.71, p = 0.004, range = 2.04-7.3 mg L-1); dissolved organic carbon (DOC) concentration (R2 = 0.79, p = 0.001, range = 1.5-4.1 mg L-1) and soluble reactive phosphorus (SRP) concentration (R2 = 0.75, p = 0.008, range = 1.9-6.2 ??g L-1) decreased with increasing disturbance intensity; and ammonia (NH 4+), nitrate (NO3-), and dissolved inorganic nitrogen (DIN) concentrations were unrelated to disturbance intensity. The increase in TSS and ISS during storms was positively correlated with disturbance (R2 = 0.78 and 0.78, p = 0.01 and 0.01, respectively); mean maximum change in SRP during storms increased with disturbance (r = 0.7, p = 0.04); and mean maximum change in NO3- during storms was marginally correlated with disturbance (r = 0.58, p = 0.06). Soil characteristics were significant predictors of baseflow DOC, SRP, and Ca 2+, but were not correlated with suspended sediment fractions, any nitrogen species, or pH. Despite the largely intact riparian zones of these headwater streams, upland soil and vegetation disturbances had clear effects on stream chemistry during baseflow and stormflow conditions. ?? ASA, CSSA, SSSA.

Journal of Environmental Quality↗

USGS2000

Comparing strengths of geographic and nongeographic classifications of stream benthic macroinvertebrates in the Mid-Atlantic Highlands, USA

The US Environmental Protection Agency’s (USEPA) Environmental Monitoring and Assessment Program (EMAP) sampled ∼500 wadeable streams in the Mid-Atlantic Highlands region of the US during the late spring of 1993 to 1995 for a variety of physical, chemical, and biological indicators of environmental condition. Eighty-eight sites that were minimally affected by human activities were chosen to determine the extent to which geographic and stream-based classifications accounted for variation in the composition of riffle macroinvertebrate assemblages. Bray–Curtis similarities among sites were calculated from the relative abundance of macroinvertebrates to assess the strength of classifications based on geography (ecoregions and catchments), habitat (slope and stream order), and water chemistry (conductivity). For comparison, a taxonomic classification (two-way indicator species analysis, TWINSPAN) and a gradient analysis (correspondence analysis, CA) were performed on the macroinvertebrate data. To assess the effect of taxonomic resolution, all analyses were completed at the family level and to lowest practical taxon. The large overall variation within and among ecoregions resulted in a low average classification strength ( CS ) of ecoregions, although some ecoregions had high CS. Stream order had the highest CS of the habitat and water chemistry classifications. Ecoregion CS increased, however, when stream sites were 1 st stratified by stream order (ecoregions nested within stream order). Nested ecoregion CS did not increase within 1 st -order streams, yet increased within 2 nd - and 3 rd -order streams. CA ordinations and TWINSPAN classification showed a clear gradient of streams along stream size (order), with a clear separation of 1 st - and 3 rd -order streams based on macroinvertebrate composition. The ordinations did not, however, show a distinct clustering of sites on the basis of ecoregions. Overall, the lowest practical taxon level of identification resulted in a clearer pattern of sites in ordination space than did family-level identification, yet only a slight improvement in the different classifications (geographic, habitat, and water chemistry) based on average similarity.

Maryland, New York, Pennsylvania, Virginia, West V↗