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851.
Sediment tracing using geochemical properties is an efficient way to identify the spatial sources of transported sediments delivered to waterways. Here, the contribution of soil sources to river bed sediments has been quantified in Emu Creek, a headwater catchment in south eastern Queensland, Australia. Soil samples were collected from the eight major rock types present in the catchment and were related to river bed sediments collected from eight sites along the main channel. Geochemistry, as characterized by 39 elemental concentrations, was measured using inductively coupled plasma mass spectrometry and inductively coupled plasma optical emission spectrometry. Three particle size fractions were examined, <10, 10–63 and 63–212 µm, with the three resultant mixing models showing divergent results. We conclude that the results of sediment mixing models based on the analysis of one grain size should not be assumed to apply across the entire particle size range of transported sediment, emphasizing the need to match the size fraction used in tracing studies to that size fraction of interest in downstream sinks. Furthermore, we present results highlighting the control transport distance plays in source dominance, with this particularly evident in the coarser fraction, where local sources dominate over more distant sources. Copyright © 2015 John Wiley & Sons, Ltd. 相似文献
852.
Scott Harlan Peter Jenniskens Michael E. Zolensky Qing‐Zhu Yin Kenneth L. Verosub Douglas J. Rowland Matthew Sanborn Magdalena Huyskens Emily R. Creager A. J. Timothy Jull 《Meteoritics & planetary science》2016,51(4):757-772
Meteorites have been found on the small Misfits Flat dry lakebed near Stagecoach, Nevada (119.382W, +39.348N). Since the first find on Sept. 22, 2013, a total of 58 stones of weathering stage W2/3 with a combined mass of 339 g have been collected in 19 visits to the area. This small (3.3 × 3.6 km) lakebed is now a newly designated dense collection area (DCA). Most meteorites were found in a small 350 × 180 m area along the north shore and most are fragments of several broken individual stones. Three of these fragments were classified as an LL4/5 of shock stage S2, now named Misfits Flat 001, one of which (stone MF33) fell 8.1 ± 1.3 ka ago based on the 14C terrestrial age, assuming it came from a 20–80 cm diameter meteoroid. In addition, a small darkly crusted meteorite MF34, now named Misfits Flat 002, was found 820 m WSW from the main mass. This meteorite is classified as an LL5 ordinary chondrite with shock stage S4/5. The meteorite is saturated in 14C at 63 dpm kg?1, suggesting it originated from the center of a 0.5 m diameter meteoroid, or deep inside a ~1.0 m meteoroid, less than 300 yr ago. Accounts exist of a fireball seen at 13:15 UT on March 2, 1895, that are consistent with the find location of Misfits Flat 002. 相似文献
853.
The Gao‐Guenie impact melt breccia—Sampling a rapidly cooled impact melt dike on an H chondrite asteroid?
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Martin Schmieder David A. Kring Timothy D. Swindle Jade C. Bond Carleton B. Moore 《Meteoritics & planetary science》2016,51(6):1022-1045
The Gao‐Guenie H5 chondrite that fell on Burkina Faso (March 1960) has portions that were impact‐melted on an H chondrite asteroid at ~300 Ma and, through later impact events in space, sent into an Earth‐crossing orbit. This article presents a petrographic and electron microprobe analysis of a representative sample of the Gao‐Guenie impact melt breccia consisting of a chondritic clast domain, quenched melt in contact with chondritic clasts, and an igneous‐textured impact melt domain. Olivine is predominantly Fo80–82. The clast domain contains low‐Ca pyroxene. Impact melt‐grown pyroxene is commonly zoned from low‐Ca pyroxene in cores to pigeonite and augite in rims. Metal–troilite orbs in the impact melt domain measure up to ~2 mm across. The cores of metal orbs in the impact melt domain contain ~7.9 wt% of Ni and are typically surrounded by taenite and Ni‐rich troilite. The metallography of metal–troilite droplets suggest a stage I cooling rate of order 10 °C s?1 for the superheated impact melt. The subsolidus stage II cooling rate for the impact melt breccia could not be determined directly, but was presumably fast. An analogy between the Ni rim gradients in metal of the Gao‐Guenie impact melt breccia and the impact‐melted H6 chondrite Orvinio suggests similar cooling rates, probably on the order of ~5000–40,000 °C yr?1. A simple model of conductive heat transfer shows that the Gao‐Guenie impact melt breccia may have formed in a melt injection dike ~0.5–5 m in width, generated during a sizeable impact event on the H chondrite parent asteroid. 相似文献
854.
Noel Gourmelen Timothy H. Dixon Falk Amelung Gina Schmalzle 《Earth and Planetary Science Letters》2011,301(1-2):337-344
We present new space geodetic data indicating that the present slip rate on the Hunter Mountain–Panamint Valley fault zone in Eastern California (5.0 ± 0.5 mm/yr) is significantly faster than geologic estimates based on fault total offset and inception time. We interpret this discrepancy as evidence for an accelerating fault and propose a new model for fault initiation and evolution. In this model, fault slip rate initially increases with time; hence geologic estimates averaged over the early stages of the fault's activity will tend to underestimate the present-day rate. The model is based on geologic data (total offset and fault initiation time) and geodetic data (present day slip rate). The model assumes a monotonic increase in slip rate with time as the fault matures and straightens. The rate increase follows a simple Rayleigh cumulative distribution. Integrating the rate-time path from fault inception to present-day gives the total fault offset. 相似文献
855.
This paper provides a review of bacterial transport experiments conducted by a multiinvestigator, multiinstitution, multidisciplinary team of researchers under the auspices of the U.S. Department of Energy (DOE). The experiments were conducted during the time period 1999-2001 at a field site near the town of Oyster, Virginia known as the South Oyster Site, and included four major experimental campaigns aimed at understanding and quantifying bacterial transport in the subsurface environment. Several key elements of the research are discussed here: (1) quantification of bacterial transport in physically, chemically, and biologically heterogeneous aquifers, (2) evaluation of the efficacy of conventional colloid filtration theory, (3) scale effects in bacterial transport, (4) development of new methods for microbial enumeration and screening for low adhesion strains, (5) application of novel hydrogeophysical techniques for aquifer characterization, and (6) experiences regarding management of a large field research effort. Lessons learned are summarized in each of these areas. The body of literature resulting from South Oyster Site research has been widely cited and continues to influence research into the controls exerted by aquifer heterogeneity on reactive transport (including microbial transport). It also served as a model (and provided valuable experience) for subsequent and ongoing highly-instrumented field research efforts conducted by DOE-sponsored investigators. 相似文献
856.
Nicole C. Lautze Thomas W. Sisson Margaret T. Mangan Timothy L. Grove 《Contributions to Mineralogy and Petrology》2011,161(2):331-347
Diffusive coarsening (Ostwald ripening) of H2O and H2O-CO2 bubbles in rhyolite and basaltic andesite melts was studied with elevated temperature–pressure experiments to investigate
the rates and time spans over which vapor bubbles may enlarge and attain sufficient buoyancy to segregate in magmatic systems.
Bubble growth and segregation are also considered in terms of classical steady-state and transient (non-steady-state) ripening
theory. Experimental results are consistent with diffusive coarsening as the dominant mechanism of bubble growth. Ripening
is faster in experiments saturated with pure H2O than in those with a CO2-rich mixed vapor probably due to faster diffusion of H2O than CO2 through the melt. None of the experimental series followed the time1/3 increase in mean bubble radius and time−1 decrease in bubble number density predicted by classical steady-state ripening theory. Instead, products are interpreted
as resulting from transient regime ripening. Application of transient regime theory suggests that bubbly magmas may require
from days to 100 years to reach steady-state ripening conditions. Experimental results, as well as theory for steady-state
ripening of bubbles that are immobile or undergoing buoyant ascent, indicate that diffusive coarsening efficiently eliminates
micron-sized bubbles and would produce mm-sized bubbles in 102–104 years in crustal magma bodies. Once bubbles attain mm-sizes, their calculated ascent rates are sufficient that they could
transit multiple kilometers over hundreds to thousands of years through mafic and silicic melt, respectively. These results
show that diffusive coarsening can facilitate transfer of volatiles through, and from, magmatic systems by creating bubbles
sufficiently large for rapid ascent. 相似文献
857.
Zahra Badrzadeh Timothy J. Barrett Jan M. Peter Domingo Gimeno Mossaieb Sabzehei Mehraj Aghazadeh 《Mineralium Deposita》2011,46(8):905-923
The Sargaz Cu–Zn massive sulfide deposit is situated in the southeastern part of Kerman Province, in the southern Sanandaj–Sirjan Zone of Iran. The stratigraphic footwall of the Sargaz deposit is Upper Triassic to Lower Jurassic (?) pillowed basalt, whereas the stratigraphic hanging wall is andesite. Mafic volcanic rocks are overlain by andesitic volcaniclastics and volcanic breccias and locally by heterogeneous debris flows. Rhyodacitic flows and volcaniclastics overlie the sequence of basaltic and andesitic rocks. Based on the bimodal nature of volcanism, the regional geologic setting and petrochemistry of the volcanic rocks, we suggest massive sulfide mineralization in the Sargaz formed in a nascent ensialic back-arc basin. The current reserves (after ancient mining) of the Sargaz deposit are 3 Mt at 1.34% Cu, 0.38% Zn, 0.08%Pb, 0.24 g/t Au, and 7 g/t Ag. The structurally dismembered massive sulfide lens is zoned from a pyrite-rich base, to a pyrite?±?chalcopyrite-rich central part, and a sphalerite–chalcopyrite-rich upper part, with a sphalerite-rich zone lateral to the upper part. The main sulfide mineral is pyrite, with lesser chalcopyrite and sphalerite. The feeder zone, comprised of a vein stockwork consists of quartz–sulfide–sericite pesudobreccia and, in the deepest part, chlorite–quartz–pyrite pesudobreccia. Footwall hydrothermal alteration extends at least 70–80 m below the massive sulfide lens and more than a hundred meters along strike from the massive sulfide lens. Jasper and Fe–Mn bearing chert horizons lateral to the sulfide deposit represent low-temperature hydrothermal precipitates of the evolving hydrothermal system. Based on mineral textures and paragenetic relationships, the growth history of the Sargaz deposit is complex and includes: (1) early precipitation of sulfides (protore) on the seafloor as precipitation of fine-grained anhedral pyrite, sphalerite, quartz, and barite; (2) anhydrite precipitation in open spaces and mineral interstices within the sulfide mound followed by its subsequent dissolution, formation of breccia textures, and mound clasts and precipitation of coarse-grained pyrite, sphalerite, tetrahedrite–tennantite, galena and barite; (3) replacement of pre-existing sulfides by chalcopyrite precipitated at higher temperatures (zone refining); (4) continued “refining” led to the dissolution of stage 3 chalcopyrite and formation of a base-metal-depleted pyrite body in the lowermost part of the massive sulfide lens; (5) carbonate veins were emplaced into the sulfide lens, replacing stage 2 barite. The δ34S composition of the sulfides ranges from +2.8‰ to +8.5‰ (average, +5.6‰) with a general increase of δ34S ratios with depth within the massive sulfide lens and underlying stockwork zone. The heavier values indicate that some of the sulfur was derived from seawater sulfate that was ultimately thermochemically reduced in deep hydrothermal reaction zones. 相似文献
858.
Relative contribution of foliar and fine root pine litter to the molecular composition of soil organic matter after in situ degradation 总被引:1,自引:0,他引:1
Stefania Mambelli Jeffrey A. Bird Gerd Gleixner Todd E. Dawson Margaret S. Torn 《Organic Geochemistry》2011,42(9):1099-1108
The influence of litter quality on soil organic matter (SOM) stabilization rate and pathways remains unclear. We used 13C/15N labeled litter addition and Curie-point pyrolysis gas chromatography–mass spectrometry combustion-isotope ratio mass spectrometry (Py–GC–MS–C–IRMS) to explore the transformation of litter with different composition and decay rate (ponderosa pine needle vs. fine root) to SOM during 18 months in a temperate conifer forest mineral (A horizon) soil. Based on 13C Py–GC–MS–C–IRMS the initial litter and bulk soil had ∼1/3 of the total pyrolysis products identified in common. The majority was related either to carbohydrates or was non-specific in origin. In bulk soil, carbohydrates had similar levels of enrichment after needle input and fine root input, while the non-specific products were more enriched after needle input. In the humin SOM fraction (260 yr C turnover time) we found only carbohydrate and alkyl C-derived compounds and greater 13C enrichment in the “carbohydrate” pool after fine root decomposition. 15N Py–GC–MS–C–IRMS of humic substances showed that root litter contributed more than needle litter to the enrichment of specific protein markers during initial decomposition.We found little evidence for the selective preservation of plant compounds considered to be recalcitrant. Our findings suggest an indirect role for decomposing plant material composition, where microbial alteration of fine root litter seems to favor greater initial stabilization of microbially derived C and N in SOM fractions with long mean turnover times, such as humin, compared to needles with a faster decay rate. 相似文献
859.
Tommy G. Jensen Timothy J. Campbell Richard A. Allard Richard Justin Small Travis A. Smith 《Ocean Dynamics》2011,61(5):657-674
The coupled ocean atmosphere mesoscale prediction system that includes the Navy Coastal Ocean Model has been configured for
the Kuroshio Extension region using multiple one-way nested high-resolution grids. The coupled model system was used to simulate
a strong cold-air outbreak event from 31 Jan to 7 Feb 2005 in good agreement with meteorological data from a surface buoy
data and QuikSCAT scatterometer winds. Latent heat fluxes and sensible heat fluxes were computed during the event with daily
averages in excess of 1,500 W/m2 and 500 W/m2, respectively, and combined instantaneous turbulent heat fluxes up to 2,300 W/m2. The largest heat fluxes were found in two large meanders of the Kuroshio and along its southern flank. Strong gradients
in turbulent heat fluxes coincided with strong sea surface temperature gradients and were maintained during the cold-air outbreak
simulation. The large turbulent heat fluxes lead to significant subtropical mode water formation during the event at a rate
about 10 Sv in the cyclonic recirculation region south of the Kuroshio. This increased the volume of core layer mode water
within the temperature range 16°C to 18°C by 10% and increased the surface area of that layer directly exposed to the atmosphere
by a factor close to 5 in the model domain. 相似文献
860.
Allison E. Ray John R. Bargar Alice C. Dohnalkova Brent M. Peyton Timothy S. Magnuson 《Geochimica et cosmochimica acta》2011,75(10):2684-6510
Microbial reduction of hexavalent uranium has been studied widely for its potential role in bioremediation and immobilization of soluble U(VI) in contaminated groundwater. More recently, some microorganisms have been examined for their role in immobilization of U(VI) via precipitation of uranyl phosphate minerals mediated by microbial phosphate release, alleviating the requirement for long-term redox control. Here, we investigated the mechanism of U(VI) removal mediated by an environmental isolate, strain UFO1, that is indigenous to the Field Research Center (FRC) in Oak Ridge, TN and has been detected in U(VI)-contaminated sediments. Changes in U(VI) speciation were examined in the presence and absence of the electron-shuttling moiety, anthraquinone-2,6-disulfonate (AQDS). Cell suspensions were capable of nearly complete removal of 100 μM U(VI) from solution within 48 h; U(VI) removal was not dependent on the presence of an exogenous electron donor or AQDS, although AQDS increased the rate of U(VI) removal. X-ray Absorption Near Edge Structure (XANES) and Extended X-ray Absorption Fine Structure (EXAFS) spectroscopic measurements indicated that U(IV) was the predominant oxidation state of uranium in cell suspensions in both the absence and presence of 100 μM AQDS. Interestingly, 17% of the cell-associated precipitates in a U(VI)-treated suspension that lacked AQDS had spectral characteristics consistent with a uranyl phosphate solid phase. The potential involvement of phosphate was consistent with observed increases in soluble phosphate concentrations over time in UFO1 cell suspensions, which suggested phosphate liberation from the cells. TEM-EDS confirmed the presence of uranyl phosphate with a U:P ratio consistent with autunite (1:1). EXAFS analyses further suggested that U(IV) was bound to low-Z neighbors such as C or P, inferred to be present as functional groups on biomass. These results suggest that strain UFO1 has the ability to facilitate U(VI) removal from solution via reductive and phosphate precipitation mechanisms. Both mechanisms offer potential for the remediation of U-contaminated sediments at the FRC or elsewhere. 相似文献