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At least 1,459 records · Page 81Linked to original sources
USGS2004

Comparison of aerodynamically and model-derived roughness lengths (zo) over diverse surfaces, central Mojave Desert, California, USA

The vulnerability of dryland surfaces to wind erosion depends importantly on the absence or the presence and character of surface roughness elements, such as plants, clasts, and topographic irregularities that diminish wind speed near the surface. A model for the friction velocity ratio has been developed to account for wind sheltering by many different types of co-existing roughness elements. Such conditions typify a monitored area in the central Mojave Desert, California, that experiences frequent sand movement and dust emission. Two additional models are used to convert the friction velocity ratio to the surface roughness length (zo) for momentum. To calculate roughness lengths from these models, measurements were made at 11 sites within the monitored area to characterize the surface roughness element. Measurements included (1) the number of roughness species (e.g., plants, small-scale topography, clasts), and their associated heights and widths, (2) spacing among species, and (3) vegetation porosity (a measurement of the spatial distribution of woody elements of a plant). Documented or estimated values of drag coefficients for different species were included in the modeling. At these sites, wind-speed profiles were measured during periods of neutral atmospheric stability using three 9-m towers with three or four calibrated anemometers on each. Modeled roughness lengths show a close correspondence (correlation coefficient, 0.84-0.86) to the aerodynamically determined values at the field sites. The geometric properties of the roughness elements in the model are amenable to measurement at much higher temporal and spatial resolutions using remote-sensing techniques than can be accomplished through laborious ground-based methods. A remote-sensing approach to acquire values of the modeled roughness length is particularly important for the development of linked surface/atmosphere wind-erosion models sensitive to climate variability and land-use changes in areas such as the southwestern United States, where surface roughness has large spatial and temporal variations. ?? 2004 Elsevier B.V. All rights reserved.

Geomorphology↗
USGS2018

Geochemical and Pb isotopic characterization of soil, groundwater, human hair, and corn samples from the Domizio Flegreo and Agro Aversano area (Campania region, Italy)

A geochemical survey was carried out to investigate metal contamination in the Domizio Littoral and Agro Aversano area (Southern Italy) by means of soil, groundwater, human hair and corn samples. Pb isotope ratios were also determined to identify the sources of metals. Specifically, the investigation focused on topsoils ( n = 1064), groundwater ( n = 26), 25 human hair ( n = 24) and corn samples ( n = 13). Topsoils have been sampled and analysed in a previous study for 53 elements (including potentially harmful ones), and determined by ICP-MS after dissolving with aqua regia. Groundwater was analysed for 72 elements by ICP-MS and by ICP-ES. Samples of human hair were prepared and analysed for 16 elements by ICP-MS. Dried corn collected at several farms were also analysed for 53 elements by ICP-MS. The isotopic ratios of 206 Pb/ 207 Pb and 208 Pb/ 207 Pb in selected topsoil ( n = 24), groundwater ( n = 9), human hair ( n = 9) and corn ( n = 4) samples were analysed from both eluates and residues to investigate possible anthropogenic contamination and geogenic contributions. All data were processed and mapped by ArcGis software to produce interpolated maps and contamination factor maps of potentially harmful elements, in accordance with Italian Environmental Law (Legislative Decree 152/06). Results show that soil sampling sites are characterized by As, Cd, Co, Cr, Cu, Hg, Pb, Se, and Zn contents exceeding the action limits established for residential land use (RAL) and, in some cases, also the action limits for industrial land use (IAL) as established by Legislative Decree 152/06. A map of contamination factors and a map showing the degrees of contamination indicate that the areas in the municipalities of Acerra, Casoria and Giugliano have been affected by considerable anthropogenic-related pollution. To interpret the isotopic data and roughly estimate proportion of Pb from an anthropogenic source we broadly defined possible natural and anthropogenic Pb end-member fields based on literature data. For example, we summarized data for Vesuvius and Campi Flegrei volcanic rocks, gasoline, and aerosol deposits. Lead isotope data show mixing between geogenic and anthropogenic sources. Topsoil, groundwater, human hair and corn samples show a greater contribution from geogenic sources like the Yellow Tuff (from Campi Flegrei) and volcanic rocks from Mt. Vesuvius. Aerosols, fly ash and gasoline (anthropogenic sources) have also been contributors. In detail, 46% of the topsoil residues, 96% of topsoil leachates, 88% of groundwater, 90% of human hair, and 25% of corn samples indicate that > 50% percent of the lead in this area can be ascribed to anthropogenic activity.

Campania region↗
USGS2016

Paleozoic magmatism and porphyry Cu-mineralization in an evolving tectonic setting in the North Qilian Orogenic Belt, NW China

The NWW-striking North Qilian Orogenic Belt records the Paleozoic accretion–collision processes in NW China, and hosts Paleozoic Cu–Pb–Zn mineralization that was temporally and spatially related to the closure of the Paleo Qilian-Qinling Ocean. The Wangdian Cu deposit is located in the eastern part of the North Qilian Orogenic Belt, NW China. Copper mineralization is spatially associated with an altered early Paleozoic porphyritic granodiorite, which intruded tonalites and volcaniclastic rocks. Alteration zones surrounding the mineralization progress outward from a potassic to a feldspar-destructive phyllic assemblage. Mineralization consists mainly of quartz-sulfide stockworks and disseminated sulfides, with ore minerals chalcopyrite, pyrite, molybdenite, and minor galena and sphalerite. Gangue minerals include quartz, orthoclase, biotite, sericite, and K-feldspar. Zircon LA-ICPMS U–Pb dating of the ore-bearing porphyritic granodiorite yielded a mean 206 Pb/ 238 U age of 444.6 ± 7.8 Ma, with a group of inherited zircons yielding a mean U–Pb age of 485 ± 12 Ma, consistent with the emplacement age (485.3 ± 6.2 Ma) of the barren precursor tonalite. Rhenium and osmium analyses of molybdenite grains returned model ages of 442.9 ± 6.8 Ma and 443.3 ± 6.2 Ma, indicating mineralization was coeval with the emplacement of the host porphyritic granodiorite. Rhenium concentrations in molybdenite (208.9–213.2 ppm) suggest a mantle Re source. The tonalities are medium-K calc-alkaline. They are characterized by enrichment of light rare-earth elements (LREEs) and large-ion lithophile elements (LILEs), depletion of heavy rare-earth elements (HREEs) and high-field-strength elements (HFSEs), and minor negative Eu anomalies. They have ε Hf ( t ) values in the range of +3.6 to +11.1, with two-stage Hf model ages of 0.67–1.13 Ga, suggesting that the ca. 485 Ma barren tonalites were products of arc magmatism incorporating melts from the mantle wedge and the lithosphere. In contrast, the 40-m.y.-younger ore-bearing porphyritic granodiorite is sub-alkaline and peraluminous. They are enriched in LREEs and LILEs, depleted in HFSEs, and show weak negative Eu anomalies. They display ε Hf ( t ) values of captured or inherited zircons in the range of +8.5 to +10.0, and younger two-stage Hf model ages of 0.78 Ga and 0.86 Ga, similar to those of ca. 485 Ma tonalite. The ca. 445 Ma zircons have ε Hf ( t ) values of −2.1 to +9.9, with two-stage Hf model ages of 0.75–1.27 Ga. Moreover, they have relatively high oxygen fugacity than that of the precursor barren tonalite. The ca. 445 Ma magmas at Wangdian thus formed in a subduction setting, and incorporated melts from the subduction-modified lithosphere that had previously been enriched by additions of chalcophile and siderophile element-rich materials by the earlier magmatism and metasomatism during the Paleo Qilian-Qinling Ocean subduction event.

North Qilian Orogenic Belt↗
USGS2018

The geochemistry of loess: Asian and North American deposits compared

Loess is widely distributed over Asia and North America and constitutes one of the most important surficial deposits that serve as terrestrial records of the Quaternary. The oldest Pleistocene loess in China is likely ∼2.6 Ma, thus spanning much or all of the Pleistocene. In North America, most loess is no older than the penultimate glacial period, with the exception of Alaska, where the record may go back to ∼3.0 Ma. On both continents, loess deposits date primarily to glacial periods, and interglacial or interstadial periods are represented by paleosols. Both glacial and non-glacial sources of silts that comprise the bulk of loess deposits are found on both continents. Although loess has been considered to be representative of the average upper continental crust, there are regionally distinctive compositions of loess in both Asia and North America. Loess deposits in Asia from Yakutia, Tajikistan, and China have compositionally distinct major element compositions, due to varying abundances of silicate minerals, carbonate minerals, and clay minerals. In North America, loess in the Mississippi River valley, the Great Plains, and Alaska are also distinguishable with regard to major element composition that reflects highly diverse source sediments. Trace element geochemistry (Sc-Th-Zr and the rare earth elements) also shows regional diversity of loess bodies, in both Asia and North America. On both continents, most loess bodies show significant contributions from later-cycle, altered sedimentary rocks, as opposed to direct derivation from igneous rocks. Further, some loess bodies have detectable contributions from mafic igneous rocks as well as major contributions from average, upper-crustal, felsic rocks. Intercalated paleosols in loess sections show geochemical compositions that differ significantly from the underlying loess parent materials. Ratios of soluble-to-insoluble elements show depletions in paleosols due to chemical weathering losses of calcite, dolomite, plagioclase, mica, apatite, and smectite. In Asia and North America, the last interglacial paleosol is more weathered than equivalent modern soils, which could be due either to a climate that was warmer and more humid, a longer period of pedogenesis, or both. In Asia, early Pleistocene loess and paleosols are both more weathered than those from the middle and late Pleistocene, forming prior to a mid-Pleistocene aridification of Asia from uplift of the Tibetan Plateau. Understanding the geochemistry of loess and paleosols can tell us much about past atmospheric circulation, past temperature and moisture regimes, and even tectonic processes.

Journal of Asian Earth Sciences↗
USGS2004

Contaminants in molting long-tailed ducks and nesting common eiders in the Beaufort Sea

In 2000, we collected blood from long-tailed ducks (Clangula hyemalis) and blood and eggs from common eiders (Somateria mollissima) at near-shore islands in the vicinity of Prudhoe Bay, Alaska, and at a reference area east of Prudhoe Bay. Blood was analyzed for trace elements and egg contents were analyzed for trace elements, organochlorine pesticides, polychlorinated biphenyls, and polycyclic aromatic hydrocarbons. Except for Se (mean=36.1 ??g/g dry weight (dw) in common eiders and 48.8 ??g/g dw in long-tailed ducks), concentrations of trace elements in blood were low and, although several trace elements differed between areas, they were not consistently higher at one location. In long-tailed ducks, Se in blood was positively correlated with activities of two serum enzymes, suggestive of an adverse effect of increasing Se levels on the liver. Although common eiders had high Se concentrations in their blood, Se residues in eggs were low (mean=2.28 ??g/g dw). Strontium and Ni were higher in eggs near Prudhoe Bay than at the reference area, but none of the other trace elements or organic contaminants in eggs differed between locations. Concentrations of Ca, Sr, Mg, and Ni differed among eggs having no visible development, early-stage embryos, or late-stage embryos. Residues of 4,4???-DDE, cis-nonachlor, dieldrin, hexachlorobenzene, oxychlordane, and trans-nonachlor were found in 100% of the common eider eggs, but at low concentrations (means of 2.35-7.45 ??g/kg wet weight (ww)). The mean total PCB concentration in eggs was 15.12 ??g/kg ww. Of PAHs tested for, residues of 1- and 2-methylnaphthalene and naphthalene were found in 100% of the eggs, at mean concentrations of 0.36-0.89 ??g/kg ww.

Alaska↗
USGS2000

Heavy metals in wild rice from northern Wisconsin

Wild rice grain samples from various parts of the world have been found to have elevated concentrations of heavy metals, raising concern for potential effects on human health. It was hypothesized that wild rice from north-central Wisconsin could potentially have elevated concentrations of some heavy metals because of possible exposure to these elements from the atmosphere or from water and sediments. In addition, no studies of heavy metals in wild rice from Wisconsin had been performed, and a baseline study was needed for future comparisons. Wild rice plants were collected from four areas in Bayfield, Forest, Langlade, Oneida, Sawyer and Wood Counties in September, 1997 and 1998 and divided into four plant parts for elemental analyses: roots, stems, leaves and seeds. A total of 194 samples from 51 plants were analyzed across the localities, with an average of 49 samples per part depending on the element. Samples were cleaned of soil, wet digested, and analyzed by ICP for Ag, As, Cd, Cr, Cu, Hg, Mg, Pb, Se and Zn. Roots contained the highest concentrations of Ag, As, Cd, Cr, Hg, Pb, and Se. Copper was highest in both roots and seeds, while Zn was highest just in seeds. Magnesium was highest in leaves. Seed baseline ranges for the 10 elements were established using the 95% confidence intervals of the medians. Wild rice plants from northern Wisconsin had normal levels of the nutritional elements Cu, Mg and Zn in the seeds. Silver, Cd, Hg, Cr, and Se were very low in concentration or within normal limits for food plants. Arsenic and Pb, however, were elevated and could pose a problem for human health. The pathway for As, Hg and Pb to the plants could be atmospheric.

Wisconsin↗
USGS1997

Petrography and geochemistry of selected lignite beds in the Gibbons Creek mine (Manning Formation, Jackson Group, Paleocene) of east-central Texas

This study examined the petrographic and geochemical characteristics of two lignite beds (3500 and 4500 beds, Manning Formation, Jackson Group, Eocene) that are mined at the Gibbons Creek mine in east-central Texas. The purpose of the study was to identify the relations among sample ash yield, coal petrography, and trace-element concentrations in lignite and adjoining rock layers of the Gibbons Creek mine. Particular interest was given to the distribution of 12 environmentally sensitive trace elements (As, Be, Cd, Cr, Co, Hg, Mn, Ni, Pb, Sb, Se, and U) that have been identified as potentially hazardous air pollutants (HAPs) in the United States Clean Air Act Amendments of 1990. Eleven lignite, floor, and rock parting samples were collected from incremental channel samples of the 3500 and 4500 beds that were exposed in a highwall of pit A3 at the Gibbons Creek mine. Short proximate and ultimate and forms of sulfur analyses were performed on all lignite samples, and lignite and rock samples were analyzed for 60 major, minor and trace elements. Representative splits of all lignite samples were ground and cast into pellets, and polished for petrographic analyses in blue-light fluorescence and reflected white light to determine liptinite, inertinite, and huminite maceral group percentages. The following observations summarize our results and conclusions about the geochemistry, petrography, and sedimentology of the 3500 and 4500 beds of the Gibbons Creek lignite deposit: (1) Weighted average dry (db) ash yield for the two beds is 29.7%, average total sulfur content is 2.6%, and average calorific value is 7832 Btu (18.22 MJ/kg). Ash yields are greatest in the lower bench (59.33% db) of the 3500 bed and in the upper bench of the 4500 bed (74.61% db). (2) For lignite samples (on a whole-coal basis), the distributions of two of the HAPs (Pb and Sb) are positively related to ash yield, probably indicating an inorganic affinity for these elements. By using cluster analysis we found that Be and Cd were poorly associated with ash yield, indicating a possible organic affinity, and that Ni, Se, Hg, U, and Pb cluster with most of the rare-earth elements. (3) The dominance of the crypto-eugelinite maceral subgroup over the crypto-humotelinite subgroup suggests that all Gibbons Creek lignites were subjected to peat-forming conditions (either biogenic or chemical) conducive to the degradation of wood cellular material into matrix gels, or that original plant material was not very woody and was prone to formation of matrix gels. The latter idea is supported by pollen studies of Gibbons Creek lignite beds; results indicate that the peat was derived in part from marsh plants low in wood tissue. (4) The occurrence of siliceous sponge spicules in the lower benches of the 3500 bed suggests the original peat in this part of the bed was deposited in standing, fresh water. (5) The petrographic data indicate that the upper sample interval of the 3500 bed contains more inertinite (3%) than the other samples studied. Increases in inertinite content in the upper part of the 3500 bed may have been associated with alteration of the peat by acids derived from the volcanic ash or could have been caused by fire, oxidation and drying, or biologic alteration of the peat in the paleo-mire.

International Journal of Coal Geology↗
USGS2004

Chapter 21 Western phosphate field - Depositional and economic deposit models

The Western Phosphate Field (WPF), composed of Permian marine sedimentary strata that cover over 300,000 km 2 in the middle Rocky Mountains of Idaho, Montana, Utah, and Wyoming in the United States, contains vast resources of phosphate mined for fertilizer and a range of other industrial applications. The richest deposits of phosphate in the WPF occur in the Meade Peak Phosphatic Shale Member of the Phosphoria Formation in southeast Idaho. Phosphate is an essential and even limiting nutrient of algal production, which occurs at the bottom of the marine food web in the oceanic photic zone. The high concentrations of phosphate and trace elements in the Phosphoria Formation reflect a low accumulation rate of diluting phases, such as terrigenous siliciclastic debris and carbonate, rather than an unusually high level of primary productivity at the time of deposition. Indeed, the mean rate of accumulation of PO 4 3 required a continuous flux of PO 4 3 into the basin and the photic zone of the water column, but only at a moderate level. This flux was maintained by upwelling of nutrient-rich seawater, imported at depth from the open ocean. Although only a fraction of the organic matter that hosted the PO 4 3 and other nutrients (NO 3 , Cd, Cu, Mo, Ni, and Zn) actually escaped oxidation in the water column, their rate of accu- mulation on the sea floor defined the basin hydrography. Rates of accumulation of Cr, U, V, and rare-earth elements by precipitation and adsorp- tion reactions identify redox conditions in the bottom water as having been denitrifying, maintained by a balance between the rate of oxidation of organic matter settling through the water column and the flux of open-ocean seawater at depth. Atmospheric mixing maintained oxygen respiration in the uppermost several tens of meters of the water column. This hydrography and seawater chemistry are present in several sedimentary envi- ronments in the ocean today. In the WPF, there is an estimated surface mineable reserve base and subeconomic resource of 7.6 billion mt, at an average grade of 24% P 2 O 5 ; a subeconomic underground- mineable resource of 17 billion mt, at a grade of 28%; and 507 billion mt of subresource- grade phosphatic material that underlie the WPF at a depth greater than 305 m. The relationship between phosphate-ore specifications and weathering suggests that significant changes in processing, with associated cost increases, will be required to extend recovery of ore below the relatively strongly weathered zone near the surface. Four open pit mines currently extract phosphate from two moderately to steeply dipping ore zones that typically contain between 20% and 35% P 2 O 5 . Although the shales are enriched in trace elements, especially As, Cd, Cr, Cu, Mo, Se, U, V, Zn, and rare-earth elements, the relative concentration of organic carbon and selected major element oxides determines the suitability of phosphate-rich rock for feed to processing plants and its other applications. Selected specifications from the four operating mines include the following: minimum P 2 O 5 of 18-20% and average of 26-27%; maximum A1 2 O 3 of 1.6-5.0%; maximum MgO of 0.3-0.6%; a CaO/P 2 O 5 ratio of 1.5-1.6; and total carbon content of 4%-5%. Weathering to a depth of as much as 100 m significantly enhances ore quality by decreasing the proportions of calcite, dolomite, and organic matter relative to carbonate fluorapatite, the primary ore mineral

Colorado, Idaho, Montana, Nebraska, North Dakota, ↗
USGS2017

Clarifying atomic weights: A 2016 four-figure table of standard and conventional atomic weights

To indicate that atomic weights of many elements are not constants of nature, in 2009 and 2011 the Commission on Isotopic Abundances and Atomic Weights (CIAAW) of the International Union of Pure and Applied Chemistry (IUPAC) replaced single-value standard atomic weight values with atomic weight intervals for 12 elements (hydrogen, lithium, boron, carbon, nitrogen, oxygen, magnesium, silicon, sulfur, chlorine, bromine, and thallium); for example, the standard atomic weight of nitrogen became the interval [14.00643, 14.00728]. CIAAW recognized that some users of atomic weight data only need representative values for these 12 elements, such as for trade and commerce. For this purpose, CIAAW provided conventional atomic weight values, such as 14.007 for nitrogen, and these values can serve in education when a single representative value is needed, such as for molecular weight calculations. Because atomic weight values abridged to four figures are preferred by many educational users and are no longer provided by CIAAW as of 2015, we provide a table containing both standard atomic weight values and conventional atomic weight values abridged to four figures for the chemical elements. A retrospective review of changes in four-digit atomic weights since 1961 indicates that changes in these values are due to more accurate measurements over time or to the recognition of the impact of natural isotopic fractionation in normal terrestrial materials upon atomic weight values of many elements. Use of the unit “u” (unified atomic mass unit on the carbon mass scale) with atomic weight is incorrect because the quantity atomic weight is dimensionless, and the unit “amu” (atomic mass unit on the oxygen scale) is an obsolete term: Both should be avoided.

Journal of Chemical Education↗
USGS2023

Attenuation of barium, strontium, cobalt, and nickel plumes formed during microbial iron-reduction in a crude-oil-contaminated aquifer

We assessed the spatial distribution of 35 elements in aquifer sediments and groundwater of a crude-oil-contaminated aquifer and show evidence of the dissolution of barium (Ba), strontium (Sr), cobalt (Co), and nickel (Ni) during hydrocarbon oxidation coupled to historic microbial Fe(III)-reduction near the oil. Trace element plumes occur in the crude-oil-contaminated aquifer, where 50% Co, 47% Ni, 24% Ba, and 15% Sr have been mobilized from the sediment near the oil into groundwater, resulting in dissolved masses >33, 18, three, and two times greater than estimated dissolved masses prior to contamination, respectively. Ba 2+ and Ni 2+ concentrations exceeded the World Health Organization’s drinking-water guidelines of 700 and 20 μg/L, respectively. Sediments attenuate trace element plumes in two geochemically distinct zones, resulting in <0.01% total trace element masses dissolved in groundwater, despite the substantial mobilization near the oil body. Geochemical modeling of the modern Fe(III)-reducing zone suggests trace elements are likely attenuated via coprecipitation with/without sorption on iron carbonate precipitates. In the suboxic transition zone at the leading edge of the plume, Fe(III)-hydroxides sorb Ba 2+ , Sr 2+ , Co 2+ , and Ni 2+ . This study emphasizes that slow but persistent biogeochemical activity can substantially alter aquifer chemistry over decadal timeframes, a phenomenon we term biogeochemical gradualism.

Minnesota↗
USGS2012

Igneous history of the Koyukuk terrane, western Alaska: Constraints on the origin, evolution, and ultimate collision of an accreted island arc terrane

The Koyukuk terrane of western Alaska consists of volcanic, volcaniclastic, and plutonic rocks which range from Late Paleozoic to Early Cretaceous in age. The terrane crops out in a U-shaped belt which is roughly paralleled by outer belts of ultramafic rocks, oceanic plate basalts and cherts, and retrograded blueschist facies rocks of continental protolith. These rocks have been interpreted as components of a volcanic arc terrane that collided with the North American continental margin in Early Cretaceous time. The Koyukuk terrane consists of four time-stratigraphic units: (1) pre-Middle Jurassic basalts, (2) Middle and Late Jurassic granitic rocks, (3) lower Lower Cretaceous volcanic rocks, and (4) upper Lower Cretaceous volcanic rocks. Limited chemical data from the basalts of unit 1 indicate that they were erupted in a nonarc tectonic environment, possibly in an oceanic island or back arc setting. Units 2, 3, and 4 have the characteristics of subduction-related volcanic rocks (i.e., depleted Nb and Ta and enriched alkaline elements, relative to the light rare earth elements). Unit 3 contains tholeiitic, calc-alkaline, and alkaline rocks with chondrite-normalized rare earth element patterns that range from flat (La N /Yb N = 1) to highly light rare earth element enriched (La N /Yb N > 15). The highly alkaline or shoshonitic lavas were erupted toward the end of unit 3 time (Valanginian) during the final stages of arc-continent collision. These alkaline lavas could have been derived by very small degrees of partial melting of a similar source to that of the earlier arc lavas. Unit 4 lavas are also alkaline or shoshonitic, but their incompatible element composition indicates that they were derived from a different source than that of the earlier arc lavas. These late alkaline lavas are chemically similar to crosscutting mid-Cretaceous plutons whose isotopic compositions (Arth et al., this issue ( a )) suggest derivation by partial melting of distinctly older subcontinental lithosphere. We speculate that the parental magmas of unit 4 lavas may also have been derived by partial melting of this subcontinental mantle which was underthrust beneath the Koyukuk arc terrane during the final stage of arc-continent collision.

Journal of Geophysical Research Solid Earth↗
USGS2012

Water-soluble material on aerosols collected within volcanic eruption clouds

In February and March of 1978, filter samplers mounted on an aircraft were used to collect the aerosol fraction of the eruption clouds from three active Guatemalan volcanoes (Fuego, Pacaya, and Santiaguito). The samples were collected on Teflon (Fluoropore) filters with a nominal pore diameter of 0.5μm. The mass of air sampled by the filters ranged from 0.15 to 6.6 kg. The particulate material collected consisted of fragments of angular silicate ash and droplets of what is interpreted as dilute H 2 SO 4 and HCl. After collection of the samples, each filter was rinsed with 60 ml of distilled-deionized water. Splits of each extract were centrifuged to remove particles greater than or equal to 0.1 μm in diameter, acidified, and analyzed for B, Ba, Be, Ca, Cd, Co, Cu, Fe, Li, Mg, Mn, Mo, Na, Pb, Si, Sr, V, and Zn by inductively coupled plasma—optical emission spectroscopy. Separate splits were analyzed for F and Cl by specific-ion-electrode methods and for U by a fission track technique. The elements dissolved in the aqueous extracts represent components of water-soluble material either formed directly in the eruption cloud or derived from interaction of ash particles and aerosol components of the plume. Calculations of enrichment factors, based upon concentration ratios, showed the elements most enriched in the extracts relative to bulk ash composition were Cd, Cu, V, F, Cl, Zn, and Pb. These elements represent a subset (with the addition of Cl and F) of elements previously reported enriched in atmospheric aerosols in remote regions as well as in volcanic areas. This suggests that some of the enriched elements were widely dispersed as volatile halides emitted from a volcanic source.

Journal of Geophysical Research - Oceans↗
USGS1999

Baseline sediment trace metals investigation: Steinhatchee River estuary, Florida, Northeast Gulf of Mexico

This Florida Geological Survey/U.S. Department of the Interior, Minerals Management Service Cooperative Study provides baseline data for major and trace metal concentrations in the sediments of the Steinhatchee River estuary. These data are intended to provide a benchmark for comparison with future metal concentration data measurements. The Steinhatchee River estuary is a relatively pristine bay located within the Big Bend Wildlife Management Area on the North Central Florida Gulf of Mexico coastline. The river flows 55 km through woodlands and planted pines before emptying into the Gulf at Deadman Harbor. Water quality in the estuary is excellent at present. There is minimal development within the watershed. The estuary is part of an extensive system of marshes that formed along the Florida Gulf coast during the Holocene marine transgression. Sediment accretion rate measurements range from 1.4 to 4.1 mm/yr on the basis of lead-210 measurements. Seventy-nine short cores were collected from 66 sample locations, representing four lithofacies: clay- and organic-rich sands, organic-rich sands, clean quartz sands, and oyster bioherms. Samples were analyzed for texture, total organic matter, total carbon, total nitrogen, clay mineralogy, and major and trace-metal content. Following these analyses, metal concentrations were normalized against geochemical reference elements (aluminum and iron) and against total weight percent organic matter. Metals were also normalized granulometrically against total weight percent fines (<0.062 mm). Concentrations were determined by inductively coupled plasma-atomic emission spectrometry (ICP-AES) for all metals except mercury. Mercury concentrations were determined by cold-flameless atomic absorption spectrometry (AAS). Granulometric measurements were made by sieve and pipette analyses. Organic matter was determined by two methods: weight loss upon ignition and elemental analysis (by Carlo-Erba Furnace) of carbon and nitrogen. X-ray diffraction was used to determine clay mineralogy. Trace-metal concentrations were best correlated when normalized with respect to sediment aluminum concentrations. Normalizations indicate that most major and trace-metal concentrations fall within 95% prediction limits of the expected value. This finding suggests that little significant metal contamination occurred within this system prior to 1994 sediment sampling. Exceptions include lead, mercury, copper, zinc, potassium, and phosphorous. Lead and mercury are elements that generally enter this watershed through atmospheric deposition; thus, anomalous levels of these metals are not necessarily associated with activities within the watershed of the Steinhatchee River estuary. Anomalous concentrations of other metals such as zinc, copper, and phosphorous probably do originate within the Steinhatchee watershed. Copper failed to correlate well with any geochemical or granulometric normalizer, and this condition was not limited to a single facies or area within the estuary. This finding may indicate copper contamination in the system. Increased zinc and copper levels may be attributed to marine paints. Phosphorous levels also appeared to be elevated in a few locations in the two marsh facies sampled. This may be due to nutrient loading from two small communities, Jena and Steinhatchee, or from the application of this element in fertilizer to reduce moisture stress to young planted pines on tree farms within the watershed.The Florida Geological Survey/US Department of the Interior, Minerals Management Service Cooperative Study provides baseline data for major and trace metal concentrations in the sediments of the Steinhatchee River estuary. The data are intended to provide a benchmark for comparison with metal concentration data measurements. Seventy nine short cores were collected from 66 sample locations and analyzed. Metal concentrations were normalized against geochemical reference elements and against total weight percen

Marine Georesources and Geotechnology↗
USGS1990

Calc-alkaline, shoshonitic, and primitive tholeiitic lavas from monogenetic volcanoes near Crater Lake, Oregon

Quaternary monogenetic volcanism in the High Cascades of Oregon is manifested by cinder cones, lava fields, and small shields. Near Crater Lake caldera, monogenetic lava compositions include: low-K (as low as 0·09% K 2 O) high-alumina olivine tholeiite (HAOT); medium-K. calc-alkaline basalt, basaltic andesite, and andesite; and shoshonitic basaltic andesite (2·1% K 2 O, 1750 ppm Sr at 54% SiO 2 ). Tholeiites have MORB-like trace element abundances except for elevated Sr, Ba, and Th and low high field strength elements (HFSE), and they represent near-primary liquids. They are similar to HAOTs from the Cascades and adjacent Basin and Range, and to many primitive basalts from intraoceanic arcs. Calc-alkaline lavas show a well-developed arc signature of high large-ion lithophile elements (LILE) and low HFSE. Their Zr and Hf concentrations are at least partly decoupled from those of Nb and Ta; HREE are low relative to HAOT. Incompatible element abundances and ratios vary widely among basaltic andesites. Some calc-alkaline lavas vented near Mount Mazama contain abundant gabbroic microxcnoliths, and are basaltic andesitic magmas contaminated with olivine gabbro. A calc-alkaline basalt and a few basaltic andesites have MgO and compatible trace element contents that suggest only minor fractionation. There appears to be a compositional continuum between primitive tholeiitic and calc-alkaline lavas. Compositional variation within suites of comagmatic primitive lavas, both tholeiitic and calc-alkaline, mainly results from different degrees of partial melting. Sources of calc-alkaline primary magmas were enriched in LILE and LREE by a subduction component and contained residual garnet, whereas sources of HAOTs had lower LILE and LREE concentrations and contained residual clinopyroxene. High and variable LILE and LREE contents of calc-alkaline lavas reflect variations in fluid-transported subduction component added to the mantle wedge, degree of partial melting, and possibly also interaction with rocks or partial melts in the lower crust. Andesites were derived from calc-alkaline basaltic andesites by fractionation of plagioclase+augite+magnetite+apatite ± orthopyroxene or olivine, commonly accompanied by assimilation. Many andesites are mixtures of andesitic or dacitic magma and a basaltic or basaltic andesitic component, or are contaminated with gabbroic material. Mingled basalt, andesite, and dacite of Williams Crater formed by multi-component, multi-stage mixing of basaltic andesitic magma, gabbro, and dacitic magma. The wide range of compositions vented from monogenetic volcanoes near Crater Lake is a result of the thick crust coupled with mild tectonic extension superimposed on a subduction-related magmatic arc.

Oregon↗
USGS1993

Emplacement and differentiation of the york haven diabase sheet, Pennsylvania

Many of the high-Ti quartz-normative tholeiitic intrusive sheets in the early Mesozoic rift basins of the Eastern USA exhibit lateral differentiation from mafic cumulate units, through diabase, to relatively evolved iron-rich rock types. We have investigated a representative example in detail, the York Haven sheet in the Gettysburg basin of south-central Pennsylvania. It ranges in thickness from 330 m to 675 m, and we have sampled it from base to top along four separate stratigraphic sections evenly spaced over the extent of the intrusion. The easternmost section (York Haven) is entirely basaltic bronzite cumulate (average 15 vol. % bronzite), whereas the westernmost (Reesers Summit) consists of diabase and low-MgO diabase with a middle to upper 'sandwich zone' of ferrogabbro. The intervening sections feature rock types transitional between the two end-member sequences. Chemically, the rock series shows a gradual east to west depletion of compatible elements (Mg, Ca, Ni, and Cr), and enrichment of incompatible elements [Ti, Fe, Na, K, P, Cu, Zr, Th, Ta, Hf, Sb, Cs, As, platinum group elements (PGEs), and rare earth elements (REEs)].We suggest two main processes for the trends observed in the York Haven sheet. First, flow differentiation during ascent and lateral injection of the parental magma produced a tongue of basaltic bronzite cumulate that thins from southeast to northwest and passes laterally into diabase, and, at the distal end of the intrusion, into low-MgO diabase. Then, in the latter stages of crystallization, densitydriven hydrothermal fluids transported incompatible elements westward, into structurally higher parts of the intrusion. Reaction of this residual aqueous fluid with partly crystallized low-MgO diabase produced a zone of ferrogabbro rich in hydrothermal replacement products (e.g., Cl-amphibole, biotite, ferrohypersthene, and skeletal ilmenite) and precipitates (e.g., quartz, fayalite, Cl-apatite, sulfides, and PGE minerals). © 1993 Oxford University Press.

Pennsylvania↗
USGS2012

Lower-crustal xenoliths from Jurassic kimberlite diatremes, upper Michigan (USA): Evidence for Proterozoic orogenesis and plume magmatism in the lower crust of the southern Superior Province

Jurassic kimberlites in the southern Superior Province in northern Michigan contain a variety of possible lower-crustal xenoliths, including mafic garnet granulites, rare garnet-free granulites, amphibolites and eclogites. Whole-rock major-element data for the granulites suggest affinities with tholeiitic basalts. P–T estimates for granulites indicate peak temperatures of 690–730°C and pressures of 9–12 kbar, consistent with seismic estimates of crustal thickness in the region. The granulites can be divided into two groups based on trace-element characteristics. Group 1 granulites have trace-element signatures similar to average Archean lower crust; they are light rare earth element (LREE)-enriched, with high La/Nb ratios and positive Pb anomalies. Most plot to the left of the geochron on a 206 Pb/ €204 Pb vs 207 Pb/ €204 Pb diagram, and there was probably widespread incorporation of Proterozoic to Archean components into the magmatic protoliths of these rocks. Although the age of the Group 1 granulites is not well constrained, their protoliths appear to be have been emplaced during the Mesoproterozoic and to be older than those for Group 2 granulites. Group 2 granulites are also LREE-enriched, but have strong positive Nb and Ta anomalies and low La/Nb ratios, suggesting intraplate magmatic affinities. They have trace-element characteristics similar to those of some Mid-Continent Rift (Keweenawan) basalts. They yield a Sm–Nd whole-rock errorchron age of 1046 ± 140 Ma, similar to that of Mid-Continent Rift plume magmatism. These granulites have unusually radiogenic Pb isotope compositions that plot above the 207 Pb/ €204 Pb vs 206 Pb/ €204 Pb growth curve and to the right of the 4·55 Ga geochron, and closely resemble the Pb isotope array defined by Mid-Continent Rift basalts. These Pb isotope data indicate that ancient continental lower crust is not uniformly depleted in U (and Th) relative to Pb. One granulite xenolith, S69-5, contains quartz, and has a unique peraluminous composition. It has the lowest εNd and εHf values of the suite. Its isotopic compositions indicate that it is significantly older than the other granulites. Broken zircon cores encased by younger overgrowths suggest that this granulite includes a large component of pre-existing sedimentary rocks. Two distinct populations of zircons from S69-5 were dated by sensitive high-resolution ion microprobe. Abundant rounded zircons yield ages of 1104 ± 42 (2σ) Ma, which coincide with the Mid-Continent Rift flood basalt eruptions. Their morphology is similar to those found in lower-crustal rocks that have undergone granulite-facies metamorphism and thus they are considered to represent the age of Group 2 granulites. Also present are less abundant elongate zircon grains that yield a mean age of 1387 ± 32 (2σ) Ma. Their elongate shapes indicate growth from a melt or fluid, possibly associated with 1·3–1·5 Ga anorogenic granite magmatism exposed in the shallow crust to the south in Wisconsin, or related to an initial encroachment of the Keweenawan plume upon the lower crust. Older ages recognized in zircon cores are less well constrained but may be related to tectono-magmatic events in the southern Superior craton. Within the studied suite only S69-5 was recognized as a remnant of the Late Archean lower crust into which the Group 1 and 2 mafic granulite precursor basalts were intruded. Collectively, the data show that the lower crust beneath northern Michigan formed in Archean times and underwent a variety of tectono-magmatic processes throughout the Proterozoic, including orogenesis, partial melting and mafic magmatic underplating in response to upwelling mantle plumes.

Michigan↗
USGS2014

Geochemical and Nd-Sr-Pb isotopic evolution of metabasites from rifting of continental lithosphere, Seward Peninsula, Alaska, and implications for paleogeographic reconstruction

The chemical character of mafic rocks from the Arctic Alaska–Chukotka terrane records rifting of continental crust during the early Paleozoic, possibly during the Ordovician. The mafic rocks are part of a metamorphosed Neoproterozoic to Devonian continental margin sequence preserved in a Mesozoic metamorphic terrane, the Nome Complex, of Seward Peninsula, Alaska. Protoliths of the mafic rocks include basalt and mafic clastic rocks, which were interlayered with calcareous, pelitic, and feldspathic sediments, and gabbro and diabase, likely feeder dikes and sills to the basalt. Major-element, trace-element, and rare-earth element (REE) analyses of these mafic rocks, together with analyses of Nd, Pb, and Sr isotopes, form two compositional groups. The two groups differ in Nb/Y (one plots as basalt, the other as alkali to subalkali basalt), TiO 2 , P 2 O 5 , and Nb (and other elements). The high-Ti group is characterized by enrichment of light REE; the low-Ti group lacks such enrichment. The trace-element and isotopic characteristics of the two groups resemble typical non-arc magmas derived from the mantle: the low-Ti group has compositions between normal mid-ocean ridge basalt (N-MORB) and enriched mid-ocean ridge basalt (E-MORB), while those of the high-Ti group are between E-MORB and ocean-island basalt (OIB). The two groups have overlapping positive values of ε Nd (+0.34 to +7.40). TiO 2 /Yb ratios suggest the high-Ti group formed from melts generated under normal thickness of continental crust, while the low-Ti group formed from melts generated at shallower conditions, presumably after rift-related crustal thinning had progressed. Geologic, paleontologic, and geochronologic characteristics of the Nome Complex support an origin along the NE margin of Baltica. The rift-related magmatism in the Nome Complex likely occurred during the opening of the Uralian ocean along that margin; by implication, related parts of the Arctic Alaska–Chukotka terrane may have experienced a similar origin.

Alaska↗
USGS2025

Origin and evolution of mafic volcanism associated with 3 m.y. of andesite production at the Goat Rocks volcanic cluster, southern Washington Cascade Range

More than 3 m.y. of mafic volcanism near the Goat Rocks volcanic cluster in the southern Washington Cascade Range, USA, lends insight into the evolution of basalts and the subarc mantle at a long-lived, major arc volcanic locus. We contribute field observations, 40 Ar/ 39 Ar dates, paleomagnetic directions, and bulk rock and mineral compositions to characterize nine mafic units that erupted in association with the Goat Rocks volcanic cluster. The time frame of mafic volcanism, ca. 3.6 Ma to 60 ka, encompasses the lifespan of the central volcanic cluster (3.1 Ma to 115 ka), with a lull from ca. 2.7 Ma to 1.4 Ma. A climactic period of voluminous mafic activity and far-traveled lava flows, including construction of the Hogback Mountain shield volcano, coincided with voluminous andesite eruptions from the central volcanic cluster. The basaltic rocks in the Goat Rocks area are calc-alkaline to barely tholeiitic and have high field strength element depletion relative to large-ion lithophile elements characteristic of calc-alkaline basalts (CAB) of the Cascade volcanic arc. Unlike at neighboring andesitic volcanic centers (Mounts Adams, St. Helens, and Rainier), no other mafic end members such as high-aluminum olivine tholeiite (HAOT) or intraplate-type basalt (IPB) are present at or near the Goat Rocks volcanic cluster, although some of the calc-alkaline basalts in this study have IPB-like affinities. The Goat Rocks mafic units exhibit two main temporal trends in composition: (1) the most primitive basalts erupted earlier, compared to less primitive and more evolved compositions later, and (2) high field strength element concentrations are higher in the younger basalt units relative to the oldest two. In contrast to these temporal trends, the mafic units define two compositional groups that recur through time, a low-Sr and a high-Sr group, each with distinct trace element and Sr and Nd isotope ratios. Although radiogenic isotope ratios are generally aligned with High Cascades CAB and HAOT, some extend toward IPB of Mount Adams and Simcoe Mountains volcanic field. Olivine-dominated crystal fractionation at shallow pressure from a small range of parent magma compositions accounts for much of the variation among the basalts and basaltic andesites. A high-pressure fractionation model is plausible for only one of the youngest basalt units (basalt of Walupt Lake volcano). Mafic recharge and crustal assimilation accounts for the incompatible-element enriched composition of basaltic andesites erupted during construction of the largest andesitic centers, further supporting sustained basalt mass flux and thermal energy driving andesite genesis. We model the most primitive members of the Goat Rocks mafic units as partial melts of successively less depleted mantle in time. Variable degrees of fluxing with fluids and melts from subduction explain the distinction between high-Sr and low-Sr groups. We propose that mantle metasomatism by ancestral subduction and fluid-flux melting is heterogeneously distributed through the local subarc mantle and played a greater role in the genesis of the high-Sr basalt group. The limited range of primitive basalt types around the Goat Rocks volcanic cluster contrasts with the much greater diversity of basalts throughout the southern Washington to northern Oregon Cascade arc. On the other hand, the central volcanic cluster encompasses nearly the entire diversity observed at neighboring composite volcanoes. In the case of the Goat Rocks area at least, and perhaps attributable to the entire region, this means that the genesis of diverse intermediate magmas is independent from and does not require vastly different parental basalt compositions.

California, Oregon, Washington↗