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At least 217 records · Page 12Linked to original sources
USGS1990

Trace elements in soil and biota in confined disposal facilities for dredged material

We studied the relation of trace element concentrations in soil to those in house mice (Mus musculus), common reed (Phragmites australis) and ladybugs (Coccinella septempunctata) at five disposal facilities for dredged material. The sites had a wide range of soil trace element concentrations, acid soils and a depauperate fauna. They were very poor wildlife habitat because they were dominated by the common reed. Bioassay earthworms exposed to surface soils from three of the five sites died, whereas those exposed to four of five soils collected a meter deep survived, presumably because the deeper, unoxidized soil, was not as acid. Concentrations of Ni and Cr in the biota from each of the sites did not seem to be related to the concentrations of the same elements in soil. Although Pb, Zn and Cu concentrations in biota were correlated with those in soil, the range of concentrations in the biota was quite small compared to that in soil. The concentrations of Pb detected in mice were about as high as the concentrations previously reported in control mice from other studies. Mice from the most contaminated site (530 ppm Pb in soil) contained only slightly more Pb (8 ppm dry wt) than did mice (2-6 ppm dry wt) from sites containing much less Pb (22-92 ppm in soil). Despite the acid soil conditions, very little Cd was incorporated into food chains. Rather, Cd was leaching from the surface soil. We concluded that even the relatively high concentrations of trace elements in the acid dredged material studied did not cause high, concentrations of trace elements in the biota.

Environmental Pollution↗
USGS1983

Scoresum - A technique for displaying and evaluating multi-element geochemical information, with examples of its use in regional mineral assessment programs

A technique called SCORESUM was developed to display a maximum of multi-element geochemical information on a minimum number of maps for mineral assessment purposes. The technique can be done manually for a small analytical data set or can be done with a computer for a large data set. SCORESUM can be used with highly censored data and can also weight samples so as to minimize the chemical differences of diverse lithologies in different parts of a given study area. The full range of reported analyses for each element of interest in a data set is divided into four categories. Anomaly scores — values of O (background), 1 (weakly anomalous), 2 (moderately anomalous), and 3 (strongly anomalous) — are substituted for all of the analyses falling into each of the four categories. A group of elements based on known or suspected association in altered or mineralized areas is selected for study and the anomaly scores for these elements are summed for each sample site and then plotted on a map. Some of the results of geochemical studies conducted for mineral assessments in two areas are briefly described. The first area, the Mokelumne Wilderness and vicinity, is a relatively small and geologically simple one. The second, the Walker Lake 1° × 2° quadrangle, is a large area that has extremely complex geology and that contains a number of different mineral deposit environments. These two studies provide examples of how the SCORESUM technique has been used (1) to enhance relatively small but anomalous areas and (2) to delineate and rank areas containing geochemical signatures for specific suites of elements related to certain types of alteration or mineralization.

Journal of Geochemical Exploration↗
USGS1994

Modes of occurrence of potentially hazardous elements in coal: Levels of confidence

The modes of occurrence of the potentially hazardous elements in coal will be of significance in any attempt to reduce their mobilization due to coal combustion. Antimony and selenium may be present in solid solution in pyrite, as minute accessory sulfides dispersed throughout the organic matrix, or in organic association. Because of these modes of occurrence it is anticipated that less than 50% of these elements will be routinely removed by conventional coal cleaning procedures. Arsenic and mercury occur primarily in late-stage coarse-grained pyrite therefore physical coal cleaning procedures should be successful in removing substantial proportions of these elements. Cadmium occurs in sphalerite and lead in galena. Both of these minerals exhibit a wide range of particle sizes and textural relations. Depending on the particle size and textural relations, physical coal cleaning may remove as little as 25% of these elements or as much as 75%. Manganese in bituminous coal occurs in carbonates, especially siderite. Physical coal cleaning should remove a substantial proportion of this element. More information is needed to elucidate the modes of occurrence of beryllium, chromium, cobalt, and nickel.

Fuel Processing Technology↗
USGS2013

Atmospheric mercury and fine particulate matter in coastal New England: implications for mercury and trace element sources in the northeastern United States

Intensive sampling of ambient atmospheric fine particulate matter was conducted at Woods Hole, Massachusetts over a four-month period from 3 April to 29 July, 2008, in conjunction with year-long deployment of the USGS Mobile Mercury Lab. Results were obtained for trace elements in fine particulate matter concurrently with determination of ambient atmospheric mercury speciation and concentrations of ancillary gasses (SO 2 , NO x , and O 3 ). For particulate matter, trace element enrichment factors greater than 10 relative to crustal background values were found for As, Bi, Cd, Cu, Hg, Pb, Sb, V, and Zn, indicating contribution of these elements by anthropogenic sources. For other elements, enrichments are consistent with natural marine (Na, Ca, Mg, Sr) or crustal (Ba, Ce, Co, Cs, Fe, Ga, La, Rb, Sc, Th, Ti, U, Y) sources, respectively. Positive matrix factorization was used together with concentration weighted air-mass back trajectories to better define element sources and their locations. Our analysis, based on events exhibiting the 10% highest PM 2.5 contributions for each source category, identifies coal-fired power stations concentrated in the U.S. Ohio Valley, metal smelting in eastern Canada, and marine and crustal sources showing surprisingly similar back trajectories, at times each sampling Atlantic coastal airsheds. This pattern is consistent with contribution of Saharan dust by a summer maximum at the latitude of Florida and northward transport up the Atlantic Coast by clockwise circulation of the summer Bermuda High. Results for mercury speciation show diurnal production of RGM by photochemical oxidation of Hg° in a marine environment, and periodic traverse of the study area by correlated RGM-SO 2 (NO x ) plumes, indicative of coal combustion sources.

Massachusetts↗
USGS2017

Leaching of trace elements from Pittsburgh coal mill rejects compared with coal combustion products from a coal-fired power plant in Ohio, USA

We investigated the leachability of elements from mill rejects from the high-sulfur, bituminous Upper Pennsylvanian Pittsburgh coal, using the synthetic groundwater leaching procedure (SGLP), long-term leaching (LTL), and the U.S. Environmental Protection Agency's (EPA's) toxicity characteristic leaching procedure (TCLP), and compared their leaching behavior with that of three coal combustion products (CCPs)—bottom ash, economizer fly ash , and fly ash—from the same coal. None of the environmentally hazardous Resource Conservation and Recovery Act of 1976 (RCRA) metals analyzed in the leachates from the mill rejects or the CCPs exceeded U.S. EPA toxicity characteristics (As, Ba, Cd, Cr, Hg, Pb, and Se). Most trace elements leached the least from mill rejects and bottom ash and leached the most from fly ash. The elements Ca, Co, Mg, Mn, and Sr, however, were more concentrated in mill reject leachates than CCP leachates. Most trace elements increased in concentration with increasing SGLP and LTL leaching duration, but As and V decreased in concentration with time in mill reject leachates, suggesting sorption or precipitation of these elements was occurring.

Ohio↗
USGS2012

Dissolved and colloidal trace elements in the Mississippi River Delta outflow after Hurricanes Katrina and Rita

The Mississippi River delta outflow region is periodically disturbed by tropical weather systems including major hurricanes, which can terminate seasonal bottom water hypoxia and cause the resuspension of shelf bottom sediments which could result in the injection of trace elements into the water column. In the summer of 2005, Hurricanes Katrina and Rita passed over the Louisiana Shelf within a month of each other. Three weeks after Rita, we collected water samples in the Mississippi River delta outflow, examining the distributions of trace elements to study the effect of Hurricanes Katrina and Rita. We observed limited stratification on the shelf and bottom waters that were no longer hypoxic. This resulted, for instance, in bottom water dissolved Mn being lower than is typically observed during hypoxia, but with concentrations still compatible with Mn–O2 trends previously reported. Interestingly, for no element were we able to identify an obvious effect of sediment resuspension on its distribution. In general, elemental distributions were compatible with previous observations in the Mississippi outflow system. Co and Re, which have not been reported for this system previously, showed behavior consistent with other systems: input for Co likely from desorption and conservative mixing for Re. For Cs, an element for which there is little information regarding its estuarine behavior, conservative mixing was also observed. Our filtration method, which allowed us to distinguish the dissolved (<0.02 μm) from colloidal (0.02–0.45 μm) phase, revealed significant colloidal fractions for Fe and Zn, only. For Fe, the colloidal phase was the dominant fraction and was rapidly removed at low salinity. Dissolved Fe, in contrast, persisted out to mid-salinities, being removed in a similar fashion to nitrate. This ability to distinguish the smaller Fe (likely dominantly organically complexed) from larger colloidal suspensates may be useful in better interpreting the bioavailablity of the Fe in estuarine systems.

Mississippi River↗
USGS2018

Mapping the relationships between trail conditions and experiential elements of long-distance hiking

Trail users that experience acceptable social and ecological conditions are more likely to act as trail stewards, exhibit proper trail etiquette, and use low-impact practices. However, the relationships between specific trail conditions and experiential elements of long-distance hiking are not well understood. Therefore, the purpose of this study was to identify how trail conditions influence particular elements of the long-distance hiking experience. The researchers used a mixed-methods approach involving semi-structured interviews ( n = 17), quantitative questionnaires ( n = 336), ecological measurements of trail conditions ( n = 21–5 km sections), and modified Recreation Suitability Mapping (RSM) techniques to quantify the relationships between five trail conditions (trail incision, muddiness, rugosity, trail width, and gradient) and four experiential elements of long-distance hiking (level of challenge, perceived impact to musculoskeletal system, valuation of tread aesthetics, and ability to maintain an ideal hiking pace). Quantified values were weighted, analyzed, and mapped using SPSS 22.0 and ArcMap 10.2.2. Significant differences exist in the scores and distributions of ecological measures across all sections, indicating that trail conditions vary significantly across sampled trail sections. Although, long-distance hikers felt all four experiential elements were important, tread aesthetics was ranked by 50.2% of sampled hikers as the most important experiential element to the overall experience. The resulting information after applying the weights suggests what particular type of experience is likely for each trail section considering the presence of trail conditions.

Appalachian Trail↗
USGS2022

Post-landing major element quantification using SuperCam laser induced breakdown spectroscopy

The SuperCam instrument on the Perseverance Mars 2020 rover uses a pulsed 1064 nm laser to ablate targets at a distance and conduct laser induced breakdown spectroscopy (LIBS) by analyzing the light from the resulting plasma. SuperCam LIBS spectra are preprocessed to remove ambient light, noise, and the continuum signal present in LIBS observations. Prior to quantification, spectra are masked to remove noisier spectrometer regions and spectra are normalized to minimize signal fluctuations and effects of target distance. In some cases, the spectra are also standardized or binned prior to quantification. To determine quantitative elemental compositions of diverse geologic materials at Jezero crater, Mars, we use a suite of 1198 laboratory spectra of 334 well-characterized reference samples. The samples were selected to span a wide range of compositions and include typical silicate rocks, pure minerals (e.g., silicates, sulfates, carbonates, oxides), more unusual compositions (e.g., Mn ore and sodalite), and replicates of the sintered SuperCam calibration targets (SCCTs) onboard the rover. For each major element (SiO 2 , TiO 2 , Al 2 O 3 , FeO T , MgO, CaO, Na 2 O, K 2 O), the database was subdivided into five “folds” with similar distributions of the element of interest. One fold was held out as an independent test set, and the remaining four folds were used to optimize multivariate regression models relating the spectrum to the composition. We considered a variety of models, and selected several for further investigation for each element, based primarily on the root mean squared error of prediction (RMSEP) on the test set, when analyzed at 3 m. In cases with several models of comparable performance at 3 m, we incorporated the SCCT performance at different distances to choose the preferred model. Shortly after landing on Mars and collecting initial spectra of geologic targets, we selected one model per element. Subsequently, with additional data from geologic targets, some models were revised to ensure results that are more consistent with geochemical constraints. The calibration discussed here is a snapshot of an ongoing effort to deliver the most accurate chemical compositions with SuperCam LIBS.

Spectrochimica Acta B↗
USGS2005

Elemental content of lichens of the Point Reyes Peninsula, northern California

The Point Reyes peninsula in northern California is about 45 km northwest of San Francisco and occasionally receives air masses from the city contributing to haze and lowered visibility. Although gaseous pollutants are not a problem, fine particulates containing carbon and other elements are measurable at the park. In this study, five lichen species were sampled along a 40-km linear transect from southeast to northwest from the town of Bolinas at the southern end of the peninsula. Elevated levels of Na and S and the Na/S ratio at localities nearer the ocean confirmed there is a definite marine aerosol influence on lichen elemental content. Elevated potassium and mercury concentrations were also found at high elevation sites that intercept fog. However, arsenic and lead were found to decrease with distance from Bolinas along the transect, suggesting these two elements originate in the fine particulate haze that enters the park from San Francisco. Concentrations of elements were not at enriched levels for other lichen species. A possible local influence of roads on element content needs further study.

California↗
USGS2001

Determination of element affinities by density fractionation of bulk coal samples

A review has been made of the various methods of determining major and trace element affinities for different phases, both mineral and organic in coals, citing their various strengths and weaknesses. These include mathematical deconvolution of chemical analyses, direct microanalysis, sequential extraction procedures and density fractionation. A new methodology combining density fractionation with mathematical deconvolution of chemical analyses of whole coals and their density fractions has been evaluated. These coals formed part of the IEA-Coal Research project on the Modes of Occurrence of Trace Elements in Coal. Results were compared to a previously reported sequential extraction methodology and showed good agreement for most elements. For particular elements (Be, Mo, Cu, Se and REEs) in specific coals where disagreement was found, it was concluded that the occurrence of rare trace element bearing phases may account for the discrepancy, and modifications to the general procedure must be made to account for these.

Fuel↗
USGS1997

Quantitative analysis of major elements in silicate minerals and glasses by micro-PIXE

The Guelph micro-PIXE facility has been modified to accommodate a second Si(Li) X-ray detector which records the spectrum due to light major elements (11 ??? Z ??? 20) with no deleterious effects from scattered 3 MeV protons. Spectra have been recorded from 30 well-characterized materials, including a broad range of silicate minerals and both natural and synthetic glasses. Sodium is mobile in some of the glasses, but not in the studied mineral lattices. The mean value of the instrumental constant H for each of the elements Mg, Al, and Si in these materials is systematically 6-8% lower than the H-value measured for the pure metals. Normalization factors are derived which permit the matrix corrections requisite for trace-element measurements in silicates to be based upon pure metal standards for Mg, Al and Si, supplemented by well-established, silicate mineral standards for the elements Na, K and Ca. Rigorous comparisons of electron microprobe and micro-PIXE analyses for the entire, 30-sample suite demonstrate the ability of micro-PIXE to produce accurate analysis for the light major elements in silicates. ?? 1997 Elsevier Science B.V.

Nuclear Instruments and Methods in Physics Researc↗
USGS1998

Elemental contaminants in the livers and ingesta of four subpopulations of the American coot (Fulica americana): An herbivorous winter migrant in San Francisco Bay

Water birds with diets high in animal foods in the San Francisco Bay area are exposed to trace elements that are potentially health impairing. Water birds with herbivorous diets have been less thoroughly examined. The concentrations of trace elements in the livers and the esophageal contents of an herbivorous water bird, the American coot ( Fulica americana ) were measured to compare levels of contaminant exposure among different locations in the Bay system and with other water birds. A total of 39 coots were collected from four sites: Napa River and Mare Island Strait in the north, Berkeley in the middle, and Coyote Creek in the south. Livers of Berkeley samples differed significantly from those of Napa River and Mare Island Strait by their greater concentrations of As and B and lower concentrations of Cu, but they seemed to be within normal ranges for birds. Otherwise the concentrations of trace elements in the livers did not differ among sites. Ingesta samples from Berkeley differed from the other sites because they tended to be higher in Al, V, and Zn. In contrast to waterfowl, livers from the herbivorous coots in San Francisco Bay showed little exposure to Cd, Hg, Pb, or Se. Coot ingesta showed few samples with measurable levels of Cd, Hg, or Se and had low levels of Pb. The herbivorous diet of coots may shield them from exposure to such elements. However, high levels of V were present in coot livers and ingesta from all four sites, suggesting adaptation to this toxic element.

California↗
USGS2004

Chapter 8 Petrogenesis and mineralogic residence of selected elements in the meade peak phosphatic shale member of the permian phosphoria formation, Southeast Idaho

The Meade Peak Phosphatic Shale Member of the Permian Phosphoria Formation hosts the ore mined by the phosphate industry of southeast Idaho. It also hosts environmentally sensitive elements (ESE) such as Se, As, Hg, Ni, Cd, Zn, and Cr. Primary chemistry, elemental distribution patterns, and mineralogy within the Meade Peak were modified by element migration and possibly the introduction of elements. Fluids moved within the Meade Peak throughout its history, although the passage of fluids was highly variable in space and time, resulting in small domains of different rock chemistry and different mineralogy. Timing of major events affecting the Meade Peak and mineral habit are used to differentiate among detrital, diagenetic, epigenetic, and supergene mineral assemblages. Cross-cutting relationships among minerals are too rare to provide much paragenetic infor- mation. Carbonate fluorapatite (CFA) occurs in several forms, but dominantly as pelloids, some of which may have formed in situ during diagenesis. The other volumetrically signifi- cant form of CFA is interstitial cement that formed during diagenesis. Beginning during diagenesis and continuing intermittently, multiple generations of carbonate (dolomite and calcite) formed overgrowths and texturally complex carbonate cements. Movement and precipitation of silica followed a similar pattern. The ammonium feldspar buddingtonite, which generally rims orthoclase, also formed during diagenesis. Bacteria apparently played a significant role during diagenesis as well as during supergene processes, resulting in extreme fractionation of S isotopes and the possible bacterially mediated formation of minerals such as glauconite and sphalerite. Catagenesis, apparently culminating in oil generation, was the last significant diagenetic change. Thrusting accompanied by fluid (oil and brine) migration began during catagenesis in the Late Jurassic or Cretaceous and continued into the early Eocene. Fluorite ± carbonate ± barite± bitumen veins formed as a result of brittle deformation and accompanying fluid movement. This fracturing event may have been associated with a period of extension and normal faulting (Neogene to Holocene). Passage of the Yellowstone hot spot to the north of the area during the Neogene is marked by silicic domes and basaltic flows. The enrichment of Hg in fracture coatings might be the result of deposition from warm fluids associated with the emplacement of the silicic domes or a generally elevated, regional thermal gradient associated with the volcanism. Many of the fracture systems are still open and continue to provide fluid pathways that are the primary depositional sites for a wide variety of supergene minerals (such as Se, efflorescent salts) and element associations (such as Hg, Cd-S, Fe-Cr-O) in which many of the ESE are concentrated. Native Se is the most commonly identified host of Se in the studied samples. The largest concentration of Se occurs in open-fracture systems that cross-cut waste rock and ore units. The age(s) of native Se formation is not known; how- ever, the latest period of Se mobility is the present. Direct measurement of efflorescent “salts” forming on new mine faces indicate that several ESE, including both Se and Zn, are concentrated on the faces soon after they are exposed. Zinc is present as hydrous sulfates, but the residence of Se in these “salts” is unknown.

Idaho↗
USGS2002

Back-extraction of trace elements from organometallic-halide extracts for determination by flameless atomic absorption spectrometry

The M ethyl isobutyl ketone- A mine syner G istic I odkte C omplex (MAGIC) extraction system offers the advantage that a large number of trace elements can be rapidly determined with a single sample preparation procedure. However, many of the elements extracted by the MAGIC system form volatile organometallic halide salts when the organic extract is heated in the graphite furnace. High concentrations of some elements such as Cu and Zn extracted by the system from anomalous geological samples produce serious interferences when certain other elements are determined by flameless atomic absorption. Stripping systems have been developed using solutions of HNO 3 , H 2 SO 4 , and CH 3 COOH individually or combined with H 2 O 2 in order to circumvent these problems. With these systems most of the elements in the organic extract can be sequentially stripped into an aqueous phase. Organometallic volatilization and the most serious interelement interferences, therefore, can be eliminated by stripping with various combinations of reagents in a series of steps.

Analytical Chemistry↗
USGS2002

Determination of thorium and of rare earth elements in cerium earth minerals and ores

The conventional oxalate method for precipitating thorium and the rare earth elements in acid solution exhibits definite solubilities of these elements. The present work was undertaken to establish conditions overcoming these solubilities and to find optimum conditions for precipitating thorium and the rare earth elements as hydroxides and sebacates. The investigations resulted in a reliable procedure applicable to samples in which the cerium group elements predominate. The oxalate precipitations are made from homogeneous solution at pH 2 by adding a prepared solution of anhydrous oxalic acid in methanol instead of the more expensive crystalline methyl oxalate. Calcium is added as a carrier. Quantitative precipitation of thorium and the rare earth elements is ascertained by further small additions of calcium to the supernatant liquid, until the added calcium precipitates as oxalate within 2 minutes. Calcium is removed by precipitating the hydroxides of thorium and rare earths at room temperature by adding ammonium hydroxide to pH > 10. Thorium is separated as the sebacate at pH 2.5, and the rare earths are precipitated with ammonium sebacate at pH 9. Maximum errors for combined weights of thorium and rare earth oxides on synthetic mixtures are ± 0.6 mg. Maximum error for separated thoria is ± 0.5 mg.

Analytical Chemistry↗
USGS1993

Finite-element mesh generation from mappable features

A vector-based geographical information system (GIS) is used to generate a variably-sized triangular element finite-element mesh from mappable features. Important digitally-mapped features are automatically linked to nodes in the finite-element model, ensuring an efficient, virtually error-free alternative to the tedious process of mesh design and data-input preparation by other methods. The procedure permits the user to work interactively with graphically-displayed hydrologic information about the study area allowing different mesh sizes to be used as needed, based on hydrologic complexity. The mesh-generaiion programs are stand-alone macros within the GIS that set up the basic data defining a finite-element mesh for many different finite-element model programs.

International Journal of Geographical Information ↗
USGS1981

Rare-earth element geochemistry of the island-arc volcanic rocks of Rabaul and Talasea, New Britain

The island-arc volcanic rocks of Rabaul and Talasea, New Britain, range in composition from basalt through rhyolite. Rare-earth elements have been determined by mass-spectrometric isotope dilution in 16 samples. Chondrite-normalized rare-earth element patterns are distinct for each volcanic center, but all are relatively flat (Ce/Yb E.F. = 1.1 to 3.0). Within each center, rare-earth element concentrations increase from basalt to dacite, and Eu anomalies become progressively more negative from basalt to dacite (Eu/Eu* = 1.0 to 0.8). Lavas inferred to contain cumulate phenocrysts show positive Eu anomalies (Eu/Eu* of up to 1.2). The observed variations are consistent with fractional crystallization of basalt or basaltic andesite by removal or accumulation of the observed phenocrysts, including olivine, plagioclase, pyroxene, and opaque minerals. Quantitative trace-element models for Talasea lavas indicate precipitation of 50 wt percent of phenocrysts from basalt to produce andesite and an additional 22 wt percent to produce dacite. A total-equilibrium model provides the best approximation to observed concentrations, implying that the process took place at a depth sufficient to allow slow cooling of the magma as precipitation proceeded. The “least fractionated” basalts and basaltic andesites are similar in rare-earth element pattern to those of corresponding type suites in other oceanic-island arcs, implying a widespread uniformity of source and process in the production of each magma type.

Geological Society of America Bulletin↗
USGS1971

Minor elements in water

A complete characterization of natural waters includes a determination of the concentrations of 30 or more minor elements. Emission spectrochemical methods are uniquely suited to the determination of a comparatively large number of minor elements, mainly those classified as heavy metals. Spectro-chemical data published by Braidech and Emory in 1935 and more recent data by Durfor and Becker, and by Barnett, Skougstad, and Miller, provide some insight into the minor-element character of the raw- and finished-water supplies of most of the major U.S. cities. Such data permit assessment of those supplies that contain either comparatively high or low concentrations of minor elements. The concentrations of many minor elements are unchanged by the municipal treatment-plant operations between the raw- and finished-water supply. On the other hand, part of the copper in a raw-water supply may be removed during treatment, even though the over-all result is a net increase in copper in the finished water. The aluminum concentration of finished water is greater than in the raw-water supply when aluminum sulfate is used as a coagulant aid. Significant amounts of iron may be removed during treatment.

Book chapter↗