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N.S. Simon

Publications and source records attributed to N.S. Simon.

16 recordsLinked to original sources
USGS2009

Phosphorus fractionation in sediment cores collected in 2005 before and after onset of an Aphanizomenon flos-aquae bloom in upper Klamath Lake, OR, USA

We tested the hypothesis that there would be measurable losses of phosphorus (P) from surficial sediments of Upper Klamath Lake (UKL), Oregon, if sediments were a source of P during an algal bloom. We compared concentrations of total and forms of P at various depths in cores collected before and after the onset of a large Aphanizomenon flos-aquae bloom. Concentrations of inorganic P were determined in extraction solutions of MgCl 2 (1 M, pH 8), citrate-dithionite-bicarbonate, and 1 M HCl. Sediments below 2 cm were dominated by residual P which is defined as total P minus inorganic P. During the study period, data from the top 2-cm of sediment indicated (a) significant decrease in total P concentration, primarily associated with iron oxyhydroxides at one site, and (b) significant increase in total P concentration associated with residual P at a second site. Data from two other sites indicated no net changes in concentrations of total P. ?? 2009 US Government.

Water, Air, & Soil Pollution↗
USGS2005

Loosely bound oxytetracycline in riverine sediments from two tributaries of the Chesapeake Bay

The fate of antibiotics that bind to riverine sediment is not well understood. A solution used in geochemical extraction schemes to determine loosely bound species in sediments, 1 M MgCl 2 (pH 8), was chosen to determine loosely bound, and potentially bioavailable, tetracycline antibiotics (TCs), including oxytetracycline (5-OH tetracycline) (OTC) in sediment samples from two rivers on the eastern shore of the Chesapeake Bay. Bottom sediments were collected at sites upstream from, at, and downstream from municipal sewage-treatment plants (STPs) situated on two natural waterways, Yellow Bank Stream, MD, and the Pocomoke River, MD. Concentrations of easily desorbed OTC ranged from 0.6 to approximately 1.2 μg g -1 dry wt sediment in Yellow Bank Stream and from 0.7 to approximately 3.3 μg g -1 dry wt sediment in the Pocomoke River. Concentrations of easily desorbable OTC were generally smaller in sediment upstream than in sediment downstream from the STP in the Pocomoke River. STPs and poultry manure are both potential sources of OTC to these streams. OTC that is loosely bound to sediment is subject to desorption. Other researchers have found desorbed TCs to be biologically active compounds.

Chesapeake Bay↗
USGS2005

The distribution of phosphorus in Popes Creek, VA, and in the Pocomoke River, MD: Two watersheds with different land management practices in the Chesapeake Bay Basin

This paper compares phosphorus (P) concentrations in sediments from two watersheds, one with, and one without, intensive animal agriculture. The watersheds are in the coastal plain of the Chesapeake Bay and have similar physiographic characteristics. Agriculture in the Pocomoke River, MD, watershed supplied 2.7 percent of all broiler chickens produced in the USA in 1997. Poultry litter is an abundant, local source of manure for crops. Broiler chickens are not produced in the Popes Creek, VA, watershed and poultry manure is, therefore, not a major source of fertilizer. The largest concentrations of P in sediment samples are found in floodplain and main-stem bottom sediment in both watersheds. Concentrations of total P and P extracted with 1N HCl are significantly larger in main-stem bottom sediments from the Pocomoke River than in main-stem bottom sediments from Popes Creek. Larger concentrations of P are associated with what are potentially redox sensitive iron oxyhydroxides in sediment samples from the Pocomoke River watershed than are associated with what are potentially redox sensitive iron oxyhydroxides in sediment samples from the Popes Creek watershed. Data for P and iron (Fe) concentrations in sediments from the Popes Creek watershed provide a numerical framework (baseline) with which to compare P and Fe concentrations in sediment from the Pocomoke River watershed. ?? Springer 2005.

Water, Air, & Soil Pollution↗
USGS2004

Bog iron formation in the Nassawango Creek watershed, Maryland, USA

The Nassawango bog ores in the modern environment for surficial geochemical processes were studied. The formation of Nassawango bog ores was suggested to be due to inorganic oxidation when groundwater rich in ferrous iron emerges into the oxic, surficial environment. It was suggested that the process, providing a phosphorus sink, may be an unrecognized benefit for mitigating nutrient loading from agricultural lands. It is found that without the effect of iron fixing bacteria, bog deposites could not form at significant rates.

Conference Paper↗
USGS1999

The distribution of, and relation among, mercury and methylmercury, organic carbon, carbonate, nitrogen and phosphorus, in periphyton of the south Florida ecosystem

Periphyton samples from Water Conservation Areas, Big Cypress National Preserve, and Everglades National Park in south Florida were analyzed for concentrations of total mercury, methylmercury, nitrogen, phosphorus, organic carbon, and inorganic carbon. Concentrations of total mercury in periphyton decrease slightly along a gradient from north‐to‐south. Both total mercury and methylmercury are positively correlated with organic carbon, nitrogen and phosphorus in periphyton. In horizontal sections of periphyton mats, total mercury concentrations tend to be largest at the tops and bottoms of the mats. Methylmercury concentrations tend to be the largest near the bottom of mats. These localized elevated concentrations of methylmercury suggest that there are “hot spots”; of methylmercury in periphyton.

Florida↗
USGS1999

Copper, lead, mercury and zinc in periphyton from the south Florida ecosystem

Periphyton samples from the Big Cypress National Preserve were analyzed for concentrations of copper, lead, zinc, mercury, and methylmercury. Concentrations of organic carbon, inorganic carbon, nitrogen, and phosphorus in periphyton samples also were determined. The samples were extracted with sodium acetate solution at a pH of 5.5 to determine exchangeable and carbonate phase metal concentrations in periphyton. Total metal concentrations in the periphyton were directly related to the degree of calcite saturation in the water column. Exchangeable and carbonate phase metal concentrations were directly related to the percent inorganic carbon in the samples. A connection between the geochemistry of trace metals and calcite precipitation and dissolution is suggested.

Toxicological and Environmental Chemistry↗
USGS1998

Data for periphyton and water samples collected from the south Florida ecosystem, 1995 and 1996

This report presents data for samples of periphyton and water collected in 1995 and 1996 from Water Conservation Areas, the Big Cypress National Preserve, and the Everglades National Park in south Florida. Periphyton samples were analyzed for concentrations of total mercury, methylmercury, nitrogen, phosphorus, organic carbon, and inorganic carbon . Water-column samples collected on the same dates as the periphyton samples were analyzed for concentrations of major ions.

Florida↗
USGS1997

Supercritical fluid carbon dioxide extraction and liquid chromatographic separation with electrochemical detection of methylmercury from biological samples

Using the coupled methods presented in this paper, methylmercury can be accurately and rapidly extracted from biological samples by modified supercritical fluid carbon dioxide and quantitated using liquid chromatography with reductive electrochemical detection. Supercritical fluid carbon dioxide modified with methanol effectively extracts underivatized methylmercury from certified reference materials Dorm-1 (dogfish muscle) and Dolt-2 (dogfish liver). Calcium chloride and water, with a ratio of 5:2 (by weight), provide the acid environment required for extracting methylmercury from sample matrices. Methylmercury chloride is separated from other organomercury chloride compounds using HPLC. The acidic eluent, containing 0.06 mol L-1 NaCl, insures the presence of methylmercury chloride and facilitates the reduction of mercury on a glassy carbon electrode. If dual glassy carbon electrodes are used, a positive peak is observed at -0.65 to -0.70 V and a negative peak is observed at -0.90V with the organomercury compounds that were tested. The practical detection limit for methylmercury is 5 X 10-8 mol L-1 (1 X 10-12 tool injected) when a 20 ??L injection loop is used.

International Journal of Environmental Analytical ↗
USGS1994

Geochemistry and solid-phase association of chromium in sediment from the Calcasieu River and estuary, Louisiana, U.S.A.

Sediment samples were collected from the lower Calcasieu River and estuary, Louisiana, in a study of the release of metals from sediments to the overlying water column. Whole samples were characterized by analyses that included: (1) determination of total sediment ammonium concentrations; (2) determination of total sediment Cr, Mn and Fe concentrations; (3) extraction of sediment with hydrogen peroxide followed by dilute hydrochloric acid to obtain recoverable metals, including oxides; and (4) extraction of sediment with hydrogen peroxide plus pyrophosphate at a pH of 7-8 to recover organically-bound Cr but not metal oxides. Concentrations of Cr, Mn and Fe in sediment interstitial water were determined. The concentrations of Cr in interstitial water could not be predicted from total sediment concentrations of Cr. Degradation of organic matter appeared to be the mechanism that caused elevated Cr concentrations in the interstitial water. Concentrations of Cr in interstitial water were positively correlated with total concentrations of ammonium in sediment. Concentrations of Cr in interstitial water that exceeded water-column concentrations of Cr were found when the total concentrations of ammonium in sediment exceeded 1 ??mol per gram wet weight. Concentrations of metals in interstitial water that are larger than metal concentrations in the water column create a potential for diffusive flux and metal enrichment of the overlying water column. ?? 1994.

Chemical Geology↗
USGS1992

Comparison of methods for the removal of organic carbon and extraction of chromium, iron and manganese from an estuarine sediment standard and sediment from the Calcasieu River estuary, Louisiana, U.S.A.

U.S. National Bureau of Standards (NBS) estuarine sediment 1646 from the Chesapeake Bay, Maryland, and surface sediment collected at two sites in the Calcasieu River estuary, Louisiana, were used to evaluate the dilute hydrochloric acid extraction of Cr, Fe and Mn from air-dried and freeze-dried samples that had been treated by one of three methods to remove organic carbon. The three methods for the oxidation and removal of organic carbon were: (1) 30% hydrogen peroxide; (2) 30% hydrogen peroxide plus 0.25 mM pyrophosphate; and (3) plasma oxidation (low-temperature ashing). There was no statistically significant difference at the 95% confidence level between air- and freeze-dried samples with respect to the percent of organic carbon removed by the three methods. Generally, there was no statistically significant difference at the 95% confidence level between air- and freeze-dried samples with respect to the concentration of Cr, Fe and Mn that was extracted, regardless of the extraction technique that was used. Hydrogen peroxide plus pyrophosphate removed the most organic carbon from sediment collected at the site in the Calcasieu River that was upstream from industrial outfalls. Plasma oxidation removed the most organic carbon from the sediment collected at a site in the Calcasieu River close to industrial outfalls and from the NBS estuarine sediment sample. Plasma oxidation merits further study as a treatment for removal of organic carbon. Operational parameters can be chosen to limit the plasma oxidation of pyrite which, unlike other Fe species, will not be dissolved by dilute hydrochloric acid. Preservation of pyrite allows the positive identification of Fe present as pyrite in sediments.

Chemical Geology↗
USGS1989

Nitrogen cycling between sediment and the shallow-water column in the transition zone of the Potomac River and Estuary. II. The role of wind-driven resuspension and adsorbed ammonium

During periods of sediment resuspension, desorption of ammonium from sediment solids can be the major pathway for enriching the water column with the ammonium that is produced by bacterial degradation of organic matter in the bottom material. This hyopthesis is based on a three-year study of diffusive flux in the transition zone of the Potomac River at a site 35 m from the Virginia shore where the average water-column depth is approximately 1 m over sandy sediment. A diffusion-controlled sampler was used to collect water samples at the interface between the water column and sediment and at several tens of centimeters into the sediment. Interstitial water concentration gradients showed that diffusive flux of ammonium from the sandy shallow-water sediments was approximately 1% of the diffusive flux of ammonium from the silty channel sediments in the same zone of the Potomac River. Organic nitrogen and bound or adsorbed ammonium were the predominant nitrogen forms in the sediment. Adsorbed ammonium concentrations ranged from nondetectable to 3·7 μmol g −1 of sediment. Concentrations of adsorbed ammonium per gram of sediment were one to three orders of magnitude more than interstitial water ammonium concentrations. Desorption of ammonium from sediment solids appeared to be the controlling factor in the degree of water-column ammonium enrichment. In laboratory experiments that simulated sediment resuspension, 40–80% of the adsorbed ammonium predicted to desorb did so after approximately 30 min of mixing. Based on calculations for 1 m 2 to a depth of 4 cm, one resuspenion event lasting minutes could mix more ammonium into the water column from desorption of ammonium from sediment solids than could be delivered to the water column by diffusive flux from shallow-water sediments in 10–1000 days and would be comparable to enrichment by ammonium diffusive flux for 5–50 days from channel sediments in the same river zone.

Maryland, Virginia↗
USGS1988

Nitrogen cycling between sediment and the shallow-water column in the transition zone of the Potomac River and estuary. I. Nitrate and ammonium fluxes

A three-year study of seasonal variation in water-column and sediment nitrogen species was conducted in the transition zone of the Potomac River 35 m from the Virginia shore at a site with an average water-column depth of approximately 1 m over sandy sediment. A diffusion-controlled sampler was used to collect water samples from the water column, at the interface between the water column and sediment, and at several tens of centimeters into the sediment. Nitrate was the predominant dissolved nitrogen species in the water column. The importance of denitrification was inferred by nitrate fluxes which were directed into the sediment from the water column during approximately 75% of the sampling periods and ranged from 0·02 to 0·69 mmol m −2 day −1 . Flux of nitrate from the sediment into the water column, ⩾0·1 mmol m −2 day −1 , due possibly to nitrification in surficial sediment, occurred during one spring and two summer sampling periods. Ammonium fluxes were less than 0·1 mmol m −2 day −1 during 90% of the sampling periods. Of the ammonium fluxes that were >0·05 mmol m −2 day −1 , all were fluxes into the sediment during sampling periods when sediment resuspension occurred, and all were into the water column during periods of calm. The mean value of ammonium flux (0·005 ± 0·05 mmol m −2 day −1 ) from the sandy, shallow-water sediments was two orders of magnitude less than the ammonium fluxes from the deeper, silty channel sediments in the same reach of the river. Diffusive flux calculations suggest that approximately one order of magnitude more nitrate than ammonium is cycled between the shallow-water column and the sandy sediment in the transition zone of the Potomac River.

Maryland, Virginia↗
USGS1987

The distribution of nitrogen species and adsorption of ammonium in sediments from the tidal Potomac River and estuary

The distribution of dissolved ammonium, adsorbed ammonium and residual, organic and total nitrogen was measured in Potomac River tidal, transition zone and lower estuary sediments to a depth of 66 cm. For these sediments, exchangeable ammonium, and thereby adsorbed ammonium concentrations, were determined directly using an ammonia electrode in alkaline sediment suspensions. Ammonia electrode data were comparable to data obtained by KCl extraction of fresh sediment. The conventional unitless ammonium adsorption coefficient, calculated as the slope of the regression line drawn when sediment-adsorbed ammonium (μmol g −1 dry wt of sediment) is plotted against interstitial water ammonium (μmol g −1 dry wt sediment), is 1·5 for this system. When a modified ammonium adsorption coefficient is calculated from sediment-adsorbed ammonium concentrations and a ratio of interstitial water ammonium and potassium concentrations, the regression equation through the data has a zero intercept and is more nearly linear than the regression equation of data based on conventional calculations. The use of a ratio including ammonium and potassium concentrations in the interstitial water term takes into account ionic strength variations in the estuary and competition between ammonium and potassium for adsorption sites.

Maryland, Virginia↗
USGS1985

Evaluation and use of a diffusion-controlled sampler for determining chemical and dissolved oxygen gradients at the sediment-water interface

Field and laboratory evaluations were made of a simple, inexpensive diffusion-controlled sampler with ports on two sides at each interval which incorporates 0.2-??m polycarbonate membrane to filter samples in situ. Monovalent and divalent ions reached 90% of equilibrium between sampler contents and the external solution within 3 and 6 hours, respectively. Sediment interstitial water chemical gradients to depths of tens of centimeters were obtained within several days after placement. Gradients were consistent with those determined from interstitial water obtained by centrifugation of adjacent sediment. Ten milliliter sample volumes were collected at 1-cm intervals to determine chemical gradients and dissolved oxygen profiles at depth and at the interface between the sediment and water column. The flux of dissolved species, including oxygen, across the sediment-water interface can be assessed more accurately using this sampler than by using data collected from benthic cores. ?? 1985 Dr W. Junk Publishers.

Hydrobiologia↗
USGS1984

Methods for the collection of geochemical data from the sediments of the tidal Potomac River and estuary and data for 1978-1980

The chemical composition of bottom sediments and their associated pore waters from the tidal Potomac River and Estuary was studied from May 1978 through June 1980. Pore waters were routinely analyzed for pH, Eh, alkalinity, and concentrations of sulfide, sulfate, phosphate, carbon, ammonium, silica, iron, manganese, chloride, sodium, potassium, calcium, and magnesium. Porosity, weight loss on ignition, and carbon, nitrogen, and phosphorus contents were determined for the solid sediments. The range of salinity and chemical composition encountered in the estuary frequently necessitated modifications of standard methods of analysis. Therefore, the methods used, their modifications, and their limitations are presented in some detail. The appendix lists the data obtained from six sampling periods. (USGS)

Open-File Report↗