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R. M. Bouse

Publications and source records attributed to R. M. Bouse.

14 recordsLinked to original sources
USGS2003

Microbial cycling of mercury in contaminated pelagic and wetland sediments of San Pablo Bay, California

San Pablo Bay is an estuary, within northern San Francisco Bay, containing elevated sediment mercury (Hg) levels because of historic loading of hydraulic mining debris during the California gold-rush of the late 1800s. A preliminary investigation of benthic microbial Hg cycling was conducted in surface sediment (0–4 cm) collected from one salt-marsh and three open-water sites. A deeper profile (0–26 cm) was evaluated at one of the open-water locations. Radiolabeled model Hg-compounds were used to measure rates of both methylmercury (MeHg) production and degradation by bacteria. While all sites and depths had similar total-Hg concentrations (0.3–0.6 ppm), and geochemical signatures of mining debris (as εNd, range: –3.08 to –4.37), in-situ MeHg was highest in the marsh (5.4±3.5 ppb) and ≤0.7 ppb in all open-water sites. Microbial MeHg production (potential rate) in 0–4 surface sediments was also highest in the marsh (3.1 ng g –1 wet sediment day –1 ) and below detection (<0.06 ng g –1 wet sediment day –1 ) in open-water locations. The marsh exhibited a methylation/demethylation (M/D) ratio more than 25× that of all open-water locations. Only below the surface 0–4-cm horizon was significant MeHg production potential evident in the open-water sediment profile (0.2–1.1 ng g –1 wet sediment day –1 ). In-situ Hg methylation rates, calculated from radiotracer rate constants, and in-situ inorganic Hg(II) concentrations compared well with potential rates. However, similarly calculated in-situ rates of MeHg degradation were much lower than potential rates. These preliminary data indicate that wetlands surrounding San Pablo Bay represent important zones of MeHg production, more so than similarly Hg-contaminated adjacent open-water areas. This has significant implications for this and other Hg-impacted systems, where wetland expansion is currently planned.

California↗
USGS2000

Linkage of bioaccumulation and biological effects to changes in pollutant loads in south San Francisco Bay

The developed world has invested billions of dollars in waste treatment since the 1970s; however, changes in ecological or biological responses are rarely associated with reductions in metal pollutants. Here we present a novel, 23-yr time series of environmental change from a San Francisco Bay mudflat located 1 km from the discharge of a suburban domestic sewage treatment plant. Samples of surface sediment, the bioindicator Macoma balthica , and metals loading data were used to establish links between discharge, bioaccumulation, and effects. Mean annual Ag concentrations in M. balthica were 106 μg/g in 1978 and 3.67 μg/g in 1998. Concentrations of Cu declined from 287 μg/g in 1980 to a minimum of 24 μg/g in 1991. Declining Cu bioaccumulation was strongly correlated with decreasing Cu loads from the plant between 1977 and 1998. Relationships with bioaccumulation and total annual precipitation suggested that inputs from nonpoint sources were most important in controlling Zn bioavailability during the same period. Ecoepidemiological criteria were used to associate failed gamete production in M. balthica to a metals-enriched environment. Reproduction persistently failed between the mid-1970s and mid-1980s; it recovered after metal contamination declined. Other potential environmental causes such as food availability, sediment chemistry, or seasonal salinity fluctuations were not related to the timing of the change in reproductive capability. The results establish an associative link, suggesting that it is important to further investigate the chemical interference of Cu and/or Ag with invertebrate reproduction at relatively moderate levels of environmental contamination.

California↗
USGS1999

Lead isotope compositions of Late Cretaceous and early Tertiary igneous rocks and sulfide minerals in Arizona: Implications for the sources of plutons and metals in porphyry copper deposits

Porphyry copper deposits in Arizona are genetically associated with Late Cretaceous and early Tertiary igneous complexes that consist of older intermediate volcanic rocks and younger intermediate to felsic intrusions. The igneous complexes and their associated porphyry copper deposits were emplaced into an Early Proterozoic basement characterized by different rocks, geologic histories, and isotopic compositions. Lead isotope compositions of the Proterozoic basement rocks define, from northwest to southeast, the Mojave, central Arizona, and southeastern Arizona provinces. Porphyry copper deposits are present in each Pb isotope province. Lead isotope compositions of Late Cretaceous and early Tertiary plutons, together with those of sulfide minerals in porphyry copper deposits and of Proterozoic country rocks, place important constraints on genesis of the magmatic suites and the porphyry copper deposits themselves. The range of age-corrected Pb isotope compositions of plutons in 12 Late Cretaceous and early Tertiary igneous complexes is 206 Pb/ 204 Pb = 17.34 to 22.66, 207 Pb/ 204 Pb = 15.43 to 15.96, and 208 Pb/ 204 Pb = 37.19 to 40.33. These Pb isotope compositions and calculated model Th/U are similar to those of the Proterozoic rocks in which the plutons were emplaced, thereby indicating that Pb in the younger rocks and ore deposits was inherited from the basement rocks and their sources. No Pb isotope differences distinguish Late Cretaceous and early Tertiary igneous complexes that contain large economic porphyry copper deposits from less rich or smaller deposits that have not been considered economic for mining. Lead isotope compositions of Late Cretaceous and early Tertiary plutons and sulfide minerals from 30 metallic mineral districts, furthermore, require that the southeastern Arizona Pb province be divided into two subprovinces. The northern subprovince has generally lower 206 Pb/ 204 Pb and higher model Th/U, and the southern subprovince has higher 206 Pb/ 204 Pb and lower model Th/U. These Pb isotope differences are inferred to result from differences in their respective post-1.7 Ga magmatic histories. Throughout Arizona, Pb isotope compositions of Late Cretaceous and early Tertiary plutons and associated sulfide minerals are distinct from those of Jurassic plutons and also middle Tertiary igneous rocks and sulfide minerals. These differences most likely reflect changes in tectonic setting and magmatic sources. Within Late Cretaceous and early Tertiary igneous complexes that host economic porphyry copper deposits, there is commonly a decrease in Pb isotope composition from older to younger plutons. This decrease in Pb isotope values with time suggests an increasing involvement of crust with lower U/Pb than average crust in the source(s) of Late Cretaceous and early Tertiary magmas. Lead isotope compositions of the youngest porphyries in the igneous complexes are similar to those in most sulfide minerals within the associated porphyry copper deposit. This Pb isotope similarity argues for a genetic link between them. However, not all Pb in the sulfide minerals in porphyry copper deposits is magmatically derived. Some sulfide minerals, particularly those that are late stage, or distal to the main orebody, or in Proterozoic or Paleozoic rocks, have elevated Pb isotope compositions displaced toward the gross average Pb isotope composition of the local country rocks. The more radiogenic isotopic compositions argue for a contribution of Pb from those rocks at the site of ore deposition. Combining the Pb isotope data with available geochemical, isotopic, and petrologic data suggests derivation of the young porphyry copper-related plutons, most of their Pb, and other metals from a hybridized lower continental crustal source. Because of the likely involvement of subduction-related mantle-derived basaltic magma in the hybridized lower crustal source, an indiscernible mantle contribution is probable in the porphyry magmas. Clearly, in addition, Pb was contributed from the local country rocks. This is most evident in sulfide minerals in veins that are late stage, hosted in Proterozoic gneiss, and/or peripheral to the porphyry copper deposit.

Economic Geology↗
USGS1999

Stable lead isotopic analyses of historic and contemporary lead contamination of San Francisco Bay estuary

Variations in stable lead isotopic composition (240Pb, 206Pb, 207Pb, 208Pb) in three sediment cores from the San Francisco Bay estuary document temporal changes in sources of lead during the past two centuries. Sediment, with lead from natural geologic sources, and relatively homogeneous lead isotopic compositions are overlain by sediments whose isotopic compositions indicate change in the sources of lead associated with anthropogenic modification of the estuary. The first perturbations of lead isotopic composition in the cores occur in the late 1800s concordant with the beginning of industrialization around the estuary. Large isotopic shifts, toward lower 206Pb/207Pb, occur after the turn of the century in both Richardson and San Pablo Bays. A similar relationship among lead isotopic compositions and lead concentrations in both Bays suggest contamination from the same source (a lead smelter). The uppermost sediments (post 1980) of all cores also have a relatively homogenous lead isotopic composition distinct from pre-anthropogenic and recent aerosol signatures. Lead isotopic compositions of leachates from fourteen surface sediments and five marsh samples from the estuary were also analyzed. These analyses suggest that the lead isotopic signature identified in the upper horizons of the cores is spatially homogeneous among recently deposited sediments throughout the estuary. Current aerosol lead isotopic compositions [Smith, D.R., Niemeyer, S., Flegal, A.R., 1992. Lead sources to California sea otters: industrial inputs circumvent natural lead biodepletion mechanisms. Environmental Research 57, 163-175] are distinct from the isotopic compositions of the surface sediments, suggesting that the major source of lead is cycling of historically contaminated sediments back through the water column. Both the upper core sediments and surface sediments apparently derive their lead predominantly from sources internal to the estuary. These results support the idea that geochemical cycling of lead between sediments and water accounts for persistently elevated lead concentrations in the water column despite 10-fold reduction of external source inputs to San Francisco Bay [Flegal, A.R., Rivera-Duarte, I., Ritson, P.I., Scelfo, G., Smith, G.J., Gordon, M., Sanudo-Wilhelmy, S.A., 1996. Metal contamination in San Francisco Waters: historic perturbations, contemporary concentrations, and future considerations in San Francisco Bay. In: Hollobaugh, J.T. (Ed.), The Ecosystem. AAAS, pp. 173-188].

California↗
USGS1993

Isotopic and trace-element constraints on mantle and crustal contributions to Siberian continental flood basalts, Noril'sk area, Siberia

We present a tightly controlled and comprehensive set of analytical data for the 250-Ma Siberian flood-basalt province. Consideration of major- and trace-element compositions, along with strontium, lead and neodymium isotopic compositions, strongly supports earlier Russian subdivision of this magmatism into three magmatic cycles, giving rise to three assemblages of eleven basalt suites in the ascending order Ivakinsky-Gudchikhinsky, Khakanchansky-Nadezhdinsky and Morongovsky-Samoedsky. Geochemical and isotopic discontinuities of varying magnitude characterize most of the boundaries between the eleven recognized basalt suites in the Noril'sk area. Although we conclude that the dominant volume of erupted magma originated from an asthenospheric mantle plume, none of the lavas is interpreted to directly represent asthenospheric melts, which would have been far more magnesian. On the basis of thermal considerations, we consider it unlikely that vast volumes of basaltic melt were produced directly from the continental lithospheric mantle beneath the Siberian craton. Moreover, there is little evidence from mantle xenoliths that the geochemical signatures of such melts would correspond to those of the Siberian flood basalts. Studies of melt migration lead us to conclude that transport of asthenospheric melt through the lithospheric mantle would be rapid, by fracture propagation. Lavas from the Gudchikhinsky suite have negligible Ta-Nb anomalies and positive ϵ Nd values and their parental magmas presumably interacted little with the continental lithospheric mantle or crust. All other lavas have negative Ta-Nb anomalies and lower ϵ Nd values that we attribute to interaction with continental crust. The model that we have developed requires discrete contributions from the plume and complex processing of all erupted magmas in the continental crust. The earliest magmas represent small percentages of melt formed in equilibrium with garnet. Over time, the percentage of melting in the source region and the volume of magma produced increased, and garnet was no longer stable in the plume source. All of the plume-derived melts initially contained more than 20 wt% MgO and became less Mg rich by fractionation of olivine as they traversed the lithospheric mantle. We conclude, however, that the most significant control on the geochemical and isotopic compositions of all the erupted lavas was processing of mantle-derived magma in crustal reservoirs during periodic replenishment, periodic tapping, continuous crystal fractionation and wallrock assimilation. Rapid eruption of an extremely large volume of processed magma that varied little in chemical and isotopic composition produced the sequence of relatively monotonous tholeiitic basalts that constitute the 2,300-m-thick third assemblage of the Siberian flood-basalt province near Noril'sk.

Geochimica et Cosmochimica Acta↗
USGS1988

Pb isotopes in sulfides from mid-ocean ridge hydrothermal sites

We report Pb isotope ratios of sulfides deposited at seven recently active mid-ocean ridge (MOR) hydrothermal vents. Sulfides from three sediment-starved sites on the Juan de Fuca Ridge contain Pb with isotope ratios identical to their local basaltic sources. Lead in two deposits from the sediment-covered Escanaba Trough, Gorda Ridge, is derived from the sediments and does not appear to contain any basaltic component. There is a range of isotope ratios in a Guaymas Basin deposit, consistent with a mixture of sediment and MOR basalt Pb. Lead in a Galapagos deposit differs slightly from known Galapagos basalt Pb isotope values. The faithful record of Pb isotope signatures of local sources in MOR sulfides indicates that isotope ratios from ancient analogues can be used as accurate reflections of ancient oceanic crustal values in ophiolite-hosted deposits and continental crustal averages in sediment-hosted deposits. The preservation of primary ophiolitic or continental crustal Pb isotope signatures in ancient MOR sulfides provides a powerful tool for investigation of crustal evolution and for "fingerprinting" ancient terranes.

Geology↗