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At least 595 records · Page 33Linked to original sources
USGS1995

Surface-water-quality assessment of the lower Kansas River Basin, Kansas and Nebraska: Distribution of trace-element concentrations in dissolved and suspended phases, streambed sediment, and fish samples, May 1987 through April 1990

The distribution of trace elements in dissolved and suspended phases, streambed sediment, and fish samples is described for principal streams in the lower Kansas River Basin, Kansas and Nebraska, from May 1987 through April 1990. Large median concentrations of dissolved lithium and strontium in the Kansas River were related to saline ground-water discharge, and large median concentrations of dissolved strontium in Mill Creek near Paxico, Kansas were related to Permian limestone and shale. Large concentrations of arsenic, chromium, and lead in water were identified downstream from three reservoirs, which may be attributed to resuspension of bed sediment in turbulent flow near the dams or release of water from near the bottom of the reservoirs. Trace elements in streambed sediments greater than background concentrations were identified downstream from the Aurora, Nebraska, wastewater-treatment plant, from industrial or urban areas near Kansas City, Kansas, and from the dam at Perry Lake, Kansas. Median and 90th-percentile concentrations of mercury in fish-tissue samples approximately doubled from 1979-86 to 1987-90. However, concentrations in samples collected during the latter period were less than the National Academy of Sciences and National Academy of Engineering 1972 criterion of 500 micrograms per kilogram for mercury in fish tissue.

Kansas, Nebraska↗
USGS1997

Geographical distribution and potential for adverse biological effects of selected trace elements and organic compounds in streambed sediment in the Connecticut, Housatonic, and Thames River basins, 1992-94

Streambed-sediment samples were collected in 1992-94 at selected sites in the Connecticut, Housatonic, and Thames River Basins to determine the geographical distribution of trace elements and organic compounds and their potential for adverse biological effects on aquatic organisms. Chromium, copper, lead, mercury, nickel, zinc, chlordane, DDT, PAHs, and PCBs were detected in samples from throughout the basins, but concentrations of these constituents generally were lowest in the northern forested drainage basins and highest in the southern urbanized drainage basins of Springfield, Massachusetts, and Hartford, New Haven and Bridgeport, Connecticut. Possible anthropogenic sources of these contaminants include industrial effluent; municipal wastewater; runoff from agricultural, urban and forested areas; and atmospheric deposition. Some organic compounds pose the greatest threat to biological organisms in terms of exceedances of sediment-quality guidelines; those compounds are present at sufficiently high concentrations to potentially cause severe effects at several locations in the basins. Some trace elements represent the most geographically widespread threat to living organisms. These exceed sediment-quality guidelines over a wider geographical area, although usually by lower ratios of contaminant concentration to sediment-quality guideline than the organic compounds.

Connecticut, Massachusetts, New Hampshire, New Yor↗
USGS2002

Assimilation and retention of selenium and other trace elements from crustacean food by juvenile striped bass (Morone saxatilis)

Estimates of the assimilation and retention of trace elements from food by fish are useful for linking toxicity with the biogeochemical cycling of these elements through aquatic food webs. Here we use pulse-chase radiotracer techniques to estimate the assimilation and retention of Se and four trace metals, Ag, Am, Zn, and Cd, by 43- and 88-d-old juvenile striped bass, Morone saxatilis, from crustacean food. Brine shrimp nauplii, Artemia franciscana , or adult copepods, Acartia tonsa , were fed radiolabeled diatoms and then fed to juvenile striped bass. Assimilation efficiencies (AEs ± SD) for 43-d-old fish were 18 ± 2%, 6 ± 1%, 23 ± 4%, 33 ± 3%, and 23 ± 2% for Ag, Am, Cd, Se, and Zn, respectively. For 88-d-old fish, the AEs were 28 ± 1%, 42 ± 5%, and 40 ± 5% for Cd, Se, and Zn, respectively. The higher AEs in the older fish may result from longer gut passage times for larger fish. The 44-d-old fish excreted 5 ± 0.8%, 4 ± 2.0%, 7 ± 0.3%, 9 ± 0.4%, and 1.3 ± 0.9% of the Ag, Am, Cd, Se, and Zn, respectively, they ingested from food per day, whereas the 88-d-old fish excreted 3 ± 1.0%, 8 ± 0.5%, and 3 ± 0.5% of the assimilated Cd, Se, and Zn per day, respectively. Predictions of steady state Se concentrations in juvenile striped bass tissues made using a biokinetic model and the measured AE and efflux rates ranged from 1.8 to 3.0 mg Se g -1 dry wt for muscle tissue and 6.8 to 11.6 mg Se g -1 dry wt for gut tissue. These predictions agreed well with average values of 2.1 and 13 mg Se g -1 dry wt measured independently in North San Francisco Bay, where elevated Se concentrations are of concern. The model results imply that the planktonic food web, including juvenile striped bass, does not transfer Se as efficiently to top consumers as does the benthic food web.

Limnology and Oceanography↗
USGS1991

Accumulation of trace elements and organochlorines by surf scoters wintering in the Pacific northwest

Selenium, cadmium, mercury, copper, manganese, zinc, aluminum, lead, PCBs and DDE were accumulated by segments of the surf scoter (Melanitta perspicillata) population that winters in the Pacific Northwest, but whether the uptake occurred on breeding and/or wintering grounds was uncertain for some contaminants. Surf scoters collected in Puget Sound and San Francisco Bay (in another study) during the same period (January 1985) contained similar concentrations of cadmium, but Alsea Bay scoters contained more. Cadmium was inversely related to both liver and body weights of Northwest scoters in January; similar weight losses were reported in experimental laboratory studies. Northwest and north San Francisco Bay scoters contained similar mercury concentrations, but those in south San Francisco Bay contained higher concentrations. San Francisco Bay scoters contained higher arsenic and selenium concentrations than those in the Northwest; however, the 43.4 ppm (geometric mean, dry wt) selenium in livers at Commencement Bay in January was above levels associated with the reproductive problems in aquatic birds at Kesterson National Wildlife Refuge. Even higher concentrations of some elements may be found in surf scoters in March, because a later collection (March) at San Francisco Bay yielded higher concentrations than found there in January. Trace element concentrations in birds at a given wintering location are variable among species and may be influenced by diet, breeding grounds, and physiology (e.g., at Commencement Bay surf scoters with a sediment-associated diet contained 50X more cadmium in their kidneys than did fish-eating western grebes [Aechmophorus occidentalis]). The numerous wildlife species that live on estuaries require further attention.

Northwestern Naturalist↗
USGS1993

Sampling and major element chemistry of the recent (A.D. 1631-1944) Vesuvius activity

Detailed sampling of the Vesuvius lavas erupted in the period A.D. 1631-1944 provides a suite of samples for comprehensive chemical analyses and related studies. Major elements (Si, Ti, Al, Fetotal, Mn, Mg, Ca, Na, K and P), volatile species (Cl, F, S, H2O+, H2O- and CO2), and ferrous iron (Fe2+) were determined for one hundred and forty-nine lavas and five tephra from the A.D. 1631-1944 Vesuvius activity. The lavas represent a relatively homogeneous suite with respect to SiO2, TiO2, FeOtotal, MnO and P2O5, but show systematic variations among MgO, K2O, Na2O, Al2O3 and CaO. The average SiO2 content is 48.0 wt.% and the rocks are classified as tephriphonolites according to their content of alkalis. All of the lavas are silica-undersaturated and are nepheline, leucite, and olivine normative. There is no systematic variation in major-element composition with time, over the period A.D. 1631-1944. The inter-eruption and intra-eruption compositional differences are the same magnitude. The lavas are highly porphyritic with clinopyroxene and leucite as the major phases. Fractionation effects are not reflected in the silica content of the lavas. The variability of MgO, K2O, Na2O, and CaO can be modelled as a relative depletion or accumulation of clinopyroxene. ?? 1993.

Journal of Volcanology and Geothermal Research↗
USGS2000

NASQAN: The design and implementation of a large-river suspended sediment and trace element flux programme

In 1996 the US Geological Survey (USGS) began a national flux-based water quality monitoring programme in the Mississippi, Columbia, Colorado, and Rio Grande basins. Suspended sediment flux estimates for periods greater than a year are generally accurate within ??15%. Discharge and suspended sediment concentrations varied much more than chemical levels. Most trace element concentrations are not elevated except Zn and Hg in the Ohio River, and Ag, Cu, Pb, Zn, Cd, Cr, Co, Ba, Mo, Sb, Hg, and Fe in the upper Columbia River, which is impacted by mining waste. The majority (???70%) of Cu, Zn, Cr, Ni, Ba, P, As, Fe, Mn, and Al are transported by suspended sediment; Sr transported seems dominated by the dissolved phase, whereas the transport of Li and TOC seem to be divided equally between both phases.In 1996 the US Geological Survey (USGS) began a national flux-based water quality monitoring programme in the Mississippi, Columbia, Colorado, and Rio Grande basins. Suspended sediment flux estimates for periods greater than a year are generally accurate within ??15%. Discharge and suspended sediment concentrations varied much more than chemical levels. Most trace element concentrations are not elevated except Zn and Hg in the Ohio River, and Ag, Cu, Pb, Zn, Cd, Cr, Co, Ba, Mo, Sb, Hg, and Fe in the upper Columbia River, which is impacted by mining waste. The majority (???70%) of Cu, Zn, Cr, Ni, Ba, P, As, Fe, Mn, and Al are transported by suspended sediment; Sr transported seems dominated by the dissolved phase, whereas the transport of Li and TOC seem to be divided equally between both phases.

Conference Paper↗
USGS2003

Changes in sediment-associated trace element concentrations in the Seine river basin (1994-2001)

In the 1980's, based on the concentrations of particulate-associated Hg, Cd, Pb, Cu and Zn relative to very low natural background levels, the Seine River Basin was one of the most impacted in the world. Over the past 20 years, there has been a general decline in these elevated concentrations that parallels declines in Paris sewage sludge trace element levels. Within the basin, marked differences in spatial and temporal geochemical patterns have been observed: (1) between major tributaries, (2) between trace elements, and (3) with stream order and population density, all of which illustrate the complexity of the geochemical processes ongoing in the basin.

Conference Paper↗
USGS2009

Defining fish nursery habitats: An application of otolith elemental fingerprinting in Tampa Bay, Florida

Fishing in Tampa Bay enhances the quality of life of the area's residents and visitors. However, people's desire to settle along the Bay's shorelines and tributaries has been detrimental to the very habitat believed to be crucial to prime target fishery species. Common snook (Centropomus undecimalis) and red drum (Sciaenops ocellatus) are part of the suite of estuarine fishes that 1) are economically or ecologically prominent, and 2) have complex life cycles involving movement between open coastal waters and estuarine nursery habitats, including nursery habitats that are located within upstream, low-salinity portions of the Bay?s tidal tributaries. We are using an emerging microchemical technique -- elemental fingerprinting of fish otoliths -- to determine the degree to which specific estuarine locations contribute to adult fished populations in Tampa Bay. In ongoing monitoring surveys, over 1,000 young-of-the-year common snook and red drum have already been collected from selected Tampa Bay tributaries. Using laser ablation-inductively coupled plasma - mass spectrometry (LA-ICP-MS), we are currently processing a subsample of these archived otoliths to identify location-specific fingerprints based on elemental microchemistry. We will then analyze older fish from the local fishery in order to match them to their probable nursery areas, as defined by young-of-the-year otoliths. We expect to find that some particularly favorable nursery locations contribute disproportionately to the fished population. In contrast, other nursery areas may be degraded, or act as 'sinks', thereby decreasing their contribution to the fish population. Habitat managers can direct strategic efforts to protect any nursery locations that are found to be of prime importance in contributing to adult stocks.

Florida↗
USGS1975

Spectrochemical determination of trace elements in galena

A semiquantitative spectrochemical method is described by means of which 10-mg samples of galena can be analyzed for their trace element content. Results on 40 elements are reported as six logarithmically spaced intervals per order of magnitude and obtained by visual comparison with standards prepared in spectrographically pure lead sulfide. Detection limits are generally between 1 and 20 ppm (except for Ce, Na, Sr, Ta, and Zn, which are 50 to 100 ppm). Replicate analyses of galena samples indicate a precision comparable to other semiquantitative spectrochemical methods used for the analysis of geochemical samples. Results obtained from the analysis of 129 galena samples are summarized.

Journal of Research of the U.S. Geological Survey↗
USGS2001

Chemical weathering of the Panola Granite: Solute and regolith elemental fluxes and the weathering rate of biotite

Present-day elemental and mineral weathering rates based on solute fluxes are compared quantitatively to past long-term rates determined from solid-state elemental fractionation in a saprolitic granite regolith at Panola, Georgia, USA. Saturated fluid flow across a low-permeability kaolin duripan controls the rate of steady-state unsaturated flow in the underlying saprolite. Water and Cl mass balances and experimental conductivities produce a minimum fluid flux density of 8x10 -2 m yr -1 and a fluid residence time of 12 years. Solute Si flux, based on pore water concentrations and infiltration rates, is 27 mmoles yr -1 , compared to a long-term flux rate of 17 mmoles yr -1 , based on regolith Si loss and reported 36 Cl dating of the regolith surface. Similarities in short- and long-term fluxes imply that parameters influencing silicate weathering, including precipitation, temperature, and vegetative cover, while not necessarily constant, have not significantly impacted Si leaching rates during the last several hundred thousand years. Linear decreases in solid-state Mg with decreasing regolith depth permit the calculation of the long-term biotite weathering rate under isovolumetric steady-state weathering conditions. A rate constant of 3x10 -17 moles m -2 s -1 is up to 5 orders of magnitude slower than that reported for experimental dissolution of biotite, implying very different reaction kinetics during natural weathering. Short-term biotite weathering fails to produce expected increases in solute Mg and K concentrations with increasing depth and fluid residence times in the regolith. This discrepancy indicates that ion exchange disequilibrium and open-system biologic uptake in an aggrading forest ecosystem are of sufficient magnitudes to overwhelm solute fluxes resulting from biotite weathering.

Georgia↗
USGS2005

187Os/188Os And Highly Siderophile Element Systematics Of Apollo 17 Aphanitic Melt Rocks

Generally chondritic relative abundances and high absolute abundances of the highly siderophile elements (HSE: Ru, Rh, Pd, Re, Os, Ir, Pt, Au) in Earth's upper mantle provide strong evidence that these elements were added to the Earth following the last major interaction between its metallic core and silicate fraction. So called "late accretion" may have added materials comprising as much as 0.8% of the total mass of the Earth and possibly a similar proportion of mass to the Moon. We have begun to study the chemical nature of late accreted materials to the Earth-Moon system by examining the HSE contained in lunar impact-melt rocks. The HSE contained in melt rocks were largely added to the Moon during the period of time from the origin of the lunar highlands crust (4.4-4.5 Ga) to the end of the late bombardment period (ca. 3.9 Ga). These materials provide the only direct chemical link to the late accretionary period. The chemical fingerprints of the HSE in late accreted materials may enable us to ascertain under what conditions and where in the solar system the late accreted materials formed. The 1870s/1880s ratios (reflecting long-term Re/Os), coupled with ratios of other HSE, can be diagnostic for identifying the nature of the impactor. A critical issue, however, will be deconvolving the exogenous from indigenous components. Herein we examine the Os isotopic and HSE systematics of Apollo 17 aphanitic melt rocks 73215 and 73255. The HSE in these rocks were likely added at ~3.9 Ga from the impactor that formed the Serenitatis basin.

Conference Paper↗
USGS2021

Interagency Ecological Program long-term monitoring element review: Pilot approach and methods development (2020)

This report describes the first-year, pilot-phase of what is intended to be a larger, multiple-year review of all IEP core long-term monitoring elements (LTMEs). Here we hope to provide evidence that the review team arrangement and communication schedule was effective at developing a framework to objectively evaluate a suite of LTMEs. We focused on developing methods for an effective review, documenting the process of methods development, and compiling recommendations for applications of these methods to future reviews. We also gathered recommendations to improve data collection, catchability-adjustment, and record keeping processes which will be useful for all LTMEs regardless of when they are to be reviewed. Although we did not complete a comprehensive review of the long-term monitoring elements due to our short timeline, we believe this report represents a substantial effort towards that review and will serve as an invaluable guide for subsequent IEP LTME reviews.

Report↗
USGS2024

Energy-related rare earth element sources

Energy-related materials such as coal, coal-bearing wastes, and coal combustion products are traditionally thought of as sources or by-products of electric power generation. Increasingly, these materials are considered resources for their content of rare earth elements (REEs) and other useful constituents. In this chapter, we examine the distribution, modes of occurrence, and relative extractability of REEs from coal-derived materials. We also consider economic factors associated with recovery of REEs from these sources. While several coal-derived sources show promise for REE recovery at the pilot scale, in all cases, REE contents are much below those of primary ores, such that extraction and concentrating the REEs require new and innovative approaches that are largely developmental. Among coal-related sources, fly ash is the most REE-enriched, as REEs from coal are strongly retained in these refractory solids remaining after coal combustion. Partitioning of coal-derived elements into fly ash has been known for decades but this has yet to be commercially exploited. A key drawback shown in this chapter is that a significant fraction of REEs in fly ash is contained in highly insoluble aluminosilicate glasses that make up the largest portion of this material. In addition to testing chemical or physical pretreatment approaches to help improve the extractability of REEs from fly ash, current research is applying modern analytical approaches to better understand the distribution of REEs on increasingly smaller scales, in the interest of targeting their recovery. Next-most REE-enriched among coal-related materials are solid waste products of coal mining and wastes from coal preparation, both of which are REE-enriched relative to coal itself. These waste coals concentrate mineralogical constituents that are excluded during mining or removed during coal preparation because they do not contribute to the heating value of coal for power generation. Recovery of REEs from coal waste has shown promise at the pilot scale and has the added benefit of converting a waste into useful constituents. Total REE contents of commercial coals are, on average, much below the 300 parts per million interest level for REE recovery set by the U.S. Department of Energy (DOE). However, as reviewed in this chapter, certain horizons within coal beds show preferential REE enrichment and could be targeted by selective mining. Beyond this, certain coals are REE-enriched overall due to their unique geologic histories involving derivation from REE-enriched sediment sources, deposition of volcanic ash during coal formation, or interaction of coal with REE-bearing fluids. Acidic drainage from abandoned coal mines is produced by the breakdown of pyrite (FeS 2 ), which is unstable in oxygenated conditions. While these acidic fluids have lower REE contents than any of the coal-based solids described above, they are proportionally enriched in certain heavy rare earths, especially yttrium (Y). Precipitates from coal-based acid-mine drainage concentrate REEs to levels that are of interest for recovery, and these are also promising sources for extraction at the pilot scale.

Book chapter↗
USGS2022

Determination and prediction of rare earth element eeochemical associations in acid mine drainage treatment wastes

Acid mine drainage (AMD) has been proposed by various researchers as a novel source of rare earth elements (REE), a group of elements that include critical metals for clean energy and modern technologies. REE tend to be sequestered in the Fe-Al-Mn-rich solids produced during the treatment of AMD. These solids are typically managed as waste, but could be a low-cost, readily available REE source. Here, results from field sampling, solids characterization, and geochemical modeling are presented to identify the mechanism(s) of REE attenuation and determine the minerals/solid phases in AMD solids that are enriched in REE. This study reveals that solids produced from low-pH AMD that was passively treated by limestone contain elevated concentrations of REE with Al, Fe, and/or Mn. AMD solid characterization via sequential extraction demonstrated that Al and Mn oxides were more abundant than Fe oxides and that the REEs are mainly associated with Al/Mn phases. Additionally, sequential extractions demonstrate that for the AMD solids evaluated, acidic and/or reducing extractions are required to mobilize the REE. Finally, the “CausticTitrationREYs.exe” geochemical equilibrium model demonstrated in this study indicates that the observed dissolved REE attenuation can be explained via surface complexation on Fe, Al, and Mn oxides/hydroxides and not by REE compound precipitation. The model accurately predicts the pH dependent removal of dissolved REE and that Al and Mn oxides/hydroxides are largely responsible for dissolved REE removal for the systems evaluated. The modeling results are consistent with the characterization results that show that Al and Mn hydroxides are important hosting phases of REEs in AMD treatment systems. The results presented here can be used to identify conditions favorable for accumulation of REE-enriched AMD solids and possible chemical treatment(s) to mobilize REE. The geochemical model can be applied to active and/or passive AMD treatment systems to predict REE attenuation with Fe, Al, and Mn during treatment and what phases may be enriched in REE. This information can be used to engineer AMD systems to produce specific phases enriched in REE. The recovery of REE from AMD solids is an opportunity to transform the environmental and economical challenge of polluted mine drainage into an asset.

Conference Paper↗
USGS2025

Assessing lunar rare earth element resources

Rare Earth Elements (REEs) are increasingly attracting attention globally due to their pivotal role in enhancing the performance of various hightech devices. Small amounts of these elements greatly improve the performance of materials, making magnets stronger, lenses clearer, lights brighter, batteries last longer, etc. Here we examine the notion that REEs from the Moon might compete with mining on Earth.

Conference Paper↗
USGS1951

List of current and planned projects of the trace elements program, U.S. Geological Survey

This summary lists the Geological Survey's current and future investigations of uranium and other elements of related interest. The titles of the investigations are grouped under the headings listed in the table of contents. Entries in each category are listed alphabetically, according to author or project leader, and numbered consecutively.

Trace Elements Investigations↗
USGS1952

Numerical list of U.S. Geological Survey trace elements reports to September 15, 1952

This report lists in numerical order U.S. Geological Survey Trace Elements Investigations and Memorandum Reports and supersedes a similar report issued in January 1952 (TEI-202). This report contains lists not only of reports that have been transmitted to the U.S. Atomic Energy Commission, that is, those reports followed by a date, but also those reports for which tentative titles were available prior to the date of completion of this list, September 14, 1952. The reports that are in preparation and subject to change in title are indicated by an asterisk. The classifications that are shown for some of the reports issued prior to 1947 are uncertain; classifications shown are based on the best information available at the time that this report was prepared. To keep the numerical lists up to date, periodic supplements will be issued. The supplementary pages will be prepared so that they can be substituted for the pages in the present report. The Geological Survey does not have additional copies for permanent distribution of most of the reports listed, but copies of many of the completed reports can be loaned to organizations or individuals who are cooperating with the Atomic Energy Commission.

Trace Elements Investigations↗
USGS1953

Numerical list of U.S. Geological Survey Trace Elements Reports to April 30, 1953

This report contains 1) a list in numerical order of U.S. Geological Survey Trace Elements Investigations and Memorandum Reports, and 2) an author index for these reports. It supercedes TEI-30, issued in November 1952. This report contains lists not only of reports that have been transmitted to the U.S Atomic Energy Commission, that is, those reports followed by a date, but also those reports for which tentative titles were available prior to the date of completion of this list, April 30, 1953. The reports that are in preparation and subject to change in title are indicated by an asterisk. The classifications that are shown for some of the reports issued prior to 1947 are uncertain: classifications shown are based on the best information available at the time that this report was prepared. The Geological Survey does not have additional copies for permanent distribution of most of the reports listed, but copies of many of the completed reports can be loaned to organizations or individuals who are cooperating with the Atomic Energy Commission.

Trace Elements Investigations↗