Post-Wisconsinan Chemical Weathering Rates and Trajectories From a 13,400-Year Sediment Core Record of Lead Isotopic Ratios in Maine

Science.gov (United States)

Perry, R. H.; Norton, S. A.; Koons, P. O.; Handley, M.

2008-12-01

Lead isotopic ratios recorded in a 5.3-m 13.4-ka 14C-dated lake sediment core from Sargent Mountain Pond, Maine (USA) are interpreted as an archive of post-glacial chemical weathering. Early weathering yielded highly radiogenic sediment from the preferential release of U and Th decay products (206Pb, 207Pb, and 208Pb) from accessory mineral phases in the catchment's predominantly-granitic till and bedrock relative to non-radiogenic 204Pb from the more abundant primary minerals. Values for 207Pb/206Pb in the sediment increased rapidly from 0.799 to 0.814 in the catchment's first 4,000 years of post-Wisconsinan weathering, and thereafter increased only slightly to just prior to the 19th century. Values for 208Pb/204Pb, 207Pb/204Pb, and 206Pb/204Pb decline over the same time-scale, as a result of decreasing radiogenic Pb being released from catchment weathering. Our results are consistent with: (1) the published interpretation of Pb isotopic variation in ferromanganese ocean crusts as a reflection of continental-scale glacial-interglacial chemical weathering cycles, (2) bench-scale whole-rock weathering experiments, and (3) soil chronosequence Pb isotope dissolution experiments and bridge the gap between short-term, mineral-scale experiments and long-term, ocean sediment records. We establish a time-scale for depletion of accessory minerals, and loss of their Pb isotopic signature at one catchment, and document the concurrent shift to slower primary mineral-controlled chemical weathering after deglaciation.

Biologically enhanced mineral weathering: what does it look like, can we model it?

Science.gov (United States)

Schulz, M. S.; Lawrence, C. R.; Harden, J. W.; White, A. F.

2011-12-01

The interaction between plants and minerals in soils is hugely important and poorly understood as it relates to the fate of soil carbon. Plant roots, fungi and bacteria inhabit the mineral soil and work symbiotically to extract nutrients, generally through low molecular weight exudates (organic acids, extracelluar polysachrides (EPS), siderophores, etc.). Up to 60% of photosynthetic carbon is allocated below ground as roots and exudates, both being important carbon sources in soils. Some exudates accelerate mineral weathering. To test whether plant exudates are incorporated into poorly crystalline secondary mineral phases during precipitation, we are investigating the biologic-mineral interface. We sampled 5 marine terraces along a soil chronosequence (60 to 225 ka), near Santa Cruz, CA. The effects of the biologic interactions with mineral surfaces were characterized through the use of Scanning Electron Microscopy (SEM). Morphologically, mycorrhizal fungi were observed fully surrounding minerals, fungal hyphae were shown to tunnel into primary silicate minerals and we have observed direct hyphal attachment to mineral surfaces. Fungal tunneling was seen in all 5 soils by SEM. Additionally, specific surface area (using a nitrogen BET method) of primary minerals was measured to determine if the effects of mineral tunneling are quantifiable in older soils. Results suggest that fungal tunneling is more extensive in the primary minerals of older soils. We have also examined the influence of organic acids on primary mineral weathering during soil development using a geochemical reactive transport model (CrunchFlow). Addition of organic acids in our models of soil development at Santa Cruz result in decreased activity of Fe and Al in soil pore water, which subsequently alters the spatial extent of primary mineral weathering and kaolinite precipitation. Overall, our preliminary modeling results suggest biological processes may be an important but underrepresented aspect of

Modeling the influence of organic acids on soil weathering

Science.gov (United States)

Lawrence, Corey R.; Harden, Jennifer W.; Maher, Kate

2014-01-01

Biological inputs and organic matter cycling have long been regarded as important factors in the physical and chemical development of soils. In particular, the extent to which low molecular weight organic acids, such as oxalate, influence geochemical reactions has been widely studied. Although the effects of organic acids are diverse, there is strong evidence that organic acids accelerate the dissolution of some minerals. However, the influence of organic acids at the field-scale and over the timescales of soil development has not been evaluated in detail. In this study, a reactive-transport model of soil chemical weathering and pedogenic development was used to quantify the extent to which organic acid cycling controls mineral dissolution rates and long-term patterns of chemical weathering. Specifically, oxalic acid was added to simulations of soil development to investigate a well-studied chronosequence of soils near Santa Cruz, CA. The model formulation includes organic acid input, transport, decomposition, organic-metal aqueous complexation and mineral surface complexation in various combinations. Results suggest that although organic acid reactions accelerate mineral dissolution rates near the soil surface, the net response is an overall decrease in chemical weathering. Model results demonstrate the importance of organic acid input concentrations, fluid flow, decomposition and secondary mineral precipitation rates on the evolution of mineral weathering fronts. In particular, model soil profile evolution is sensitive to kaolinite precipitation and oxalate decomposition rates. The soil profile-scale modeling presented here provides insights into the influence of organic carbon cycling on soil weathering and pedogenesis and supports the need for further field-scale measurements of the flux and speciation of reactive organic compounds.

The role of chemical weathering in the neutralization of acid rain

International Nuclear Information System (INIS)

Asolekar, S.R.

1991-01-01

Chemical weathering of soils/minerals is an important process which controls the long-term neutralization of acid rain as well as the quality of surface water, ground water, and oceans. Few laboratory studies have been conducted to evaluate the response of real whole soils or soil fractions to acidification. In this research experiments were performed in a laboratory semi-continuous pH-stat reactor over the pH range 2.7 to 4.7 using Band C-horizon soil fractions from the Bear Brook Watershed, Maine, and in presence/absence of 1 to 20 mmol/L oxalate ligand in the bulk solution. Acid consumption rate and the corresponding release rates of sodium, calcium, magnesium, aluminum, iron, and silica were monitored in the laboratory reactor. Both H + -ion and oxalate promoted weathering rates were fractional order based on the concentration in bulk solution. The mixed kinetic model for the soils is: WR T = WR H + WR ox = K H (H + ) m + K ox [OX TD ] p , where m and p are fractional orders. The hydrogen ion consumption rates were approximately equal to cation release rates on an equivalent basis for hydrogen ion promoted weathering situations where secondary precipitation was unlikely (pH < 4.7) as well as for weathering of C-horizon light fraction at pH 4.0 and oxalate concentration 1 and 5 mmol/L. The relative proportions of released species were in the neighborhood of stoichiometric ratios of bulk soil chemistry for weatherable minerals in Band C-horizon soil fractions. The experimental ratios of H/Si, Al/Si, Fe/Si, Ca/Si, Na/Si, and Mg/Si for linear weathering rates of Band C-horizon soil fractions were fairly constant in the presence and absence of oxalate ligand and strongly suggested that silica may be used as a tracer for primary mineral weathering assuming quartz is inert

Predicting soil formation on the basis of transport-limited chemical weathering

Science.gov (United States)

Yu, Fang; Hunt, Allen Gerhard

2018-01-01

Soil production is closely related to chemical weathering. It has been shown that, under the assumption that chemical weathering is limited by solute transport, the process of soil production is predictable. However, solute transport in soil cannot be described by Gaussian transport. In this paper, we propose an approach based on percolation theory describing non-Gaussian transport of solute to predict soil formation (the net production of soil) by considering both soil production from chemical weathering and removal of soil from erosion. Our prediction shows agreement with observed soil depths in the field. Theoretical soil formation rates are also compared with published rates predicted using soil age-profile thickness (SAST) method. Our formulation can be incorporated directly into landscape evolution models on a point-to-point basis as long as such models account for surface water routing associated with overland flow. Further, our treatment can be scaled-up to address complications associated with continental-scale applications, including those from climate change, such as changes in vegetation, or surface flow organization. The ability to predict soil formation rates has implications for understanding Earth's climate system on account of the relationship to chemical weathering of silicate minerals with the associated drawdown of atmospheric carbon, but it is also important in geomorphology for understanding landscape evolution, including for example, the shapes of hillslopes, and the net transport of sediments to sedimentary basins.

Tectonic uplift and denudation rate influence soil chemical weathering intensity in a semi-arid environment, southeast Spain: physico-chemical and mineralogical evidence

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Ameijeiras-Mariño, Yolanda; Opfergelt, Sophie; Schoonejans, Jérôme; Vanacker, Veerle; Sonnet, Philippe; Delmelle, Pierre

2015-04-01

Tectonic uplift is known to influence denudation rates. Denudation, including chemical weathering and physical erosion, affects soil production rates and weathering intensities. At topographic steady state, weathering can be transport- or weathering-limited. In the transport-limited regime, low denudation rates should lead to comparatively high weathering intensities, while in the weathering-limited case high denudation rates are associated with lower weathering intensities. Here, we test if this relationship applies to semi-arid environments where chemical weathering is generally slow. Three catchments (EST, FIL and CAB) were studied in the Internal Zone of the Betic Cordillera in southeast Spain, spanning a range of increasing uplift rates (10-170 mm/kyr) and increasing denudation rates (20-250 mm/kyr) from EST to CAB. In each catchment, two ridgetop soil profiles were sampled down to the bedrock. The three catchments have similar vegetation and climatic conditions, with precipitation of 250- 315 mm/yr and mean annual temperature of 15-17 °C. The mineralogy of the bedrock, as determined by XRD, is similar across the three catchments and is characterized by the presence of quartz, muscovite, clinochlore, biotite and plagioclase. This primary mineral assemblage is also found in the catchment soils, indicating that the soils studied derive from the same parent material. The soil clay-size fraction is dominated by kaolinite, vermiculite and illite. However, the proportions of the soil primary and secondary minerals vary between the catchment sites. The abundance of biotite decreases from CAB (14%) to EST (4%), whereas the quartz and clay contents show an opposite tendency (from 30 to 69% and 9.9 to 14.3%, respectively). Further, the abundance of vermiculite increases from CAB to EST. The results are interpreted in terms of increasing weathering intensity from CAB to EST by weathering of biotite into vermiculite and enrichment of soils on more weathering resistant

Soil Chemical Weathering and Nutrient Budgets along an Earthworm Invasion Chronosequence in a Northern Minnesota Forest

Science.gov (United States)

Resner, K. E.; Yoo, K.; Sebestyen, S. D.; Aufdenkampe, A. K.; Lyttle, A.; Weinman, B. A.; Blum, A.; Hale, C. M.

2011-12-01

We are investigating the impact of exotic earthworms on the rate of nutrient and ion release from soil chemical weathering along an ~200 m invasion chronosequence in a northern Minnesota sugar maple forest. The earthworms belong to three ecological groups that represent different feeding and burrowing behaviors, all of which were introduced from Europe to the previously earthworm-free Great Lakes Region through fishing and agricultural activities. As earthworms digest and mix the soil, we hypothesize that they significantly alter chemical weathering processes by incorporating mineral surfaces to new geochemical environments in their intestines and at different soil depths. The effect of mixing on soil morphology is dramatic, but biogeochemical changes remain largely unknown and therefore are poorly coupled to the current and potential changes in forest ecosystems under the threat of exotic earthworms. We analyze the activities of short-lived isotopes 137-Cs and 210-Pb along with the inorganic chemistry of soil, water, and leaf litter across an invasion transect and link these measurements to the biomass and species composition of exotic earthworms. Earthworms vertically relocate minerals and organic matter largely within the top ~10 cm, which is reflected in the depth profiles of the short-lived isotopes. Among the inorganic nutrients analyzed, Ca is of particular interest due to sugar maple's aptitude for recycling Ca. Fractional mass loss values (tau) of Ca, relative to the soil's parent material, show an enrichment factor of 14 in the least invaded A horizon soils. However, such a high enrichment factor declines dramatically in the heavily invaded soils, suggesting that earthworm activities contribute to leaching Ca. In contrast, the enrichment factor of Fe increases with greater degrees of earthworm invasion, which is consistent with the extraction chemistry data showing greater quantities of pedogenic crystalline iron oxides and greater mineral specific

Long-term evolution of radio-active waste storage in geological formations: analogy with the weathering of mineral deposits

International Nuclear Information System (INIS)

Cantinolle, P.; Griffault, L.; Jebrak, M.

1986-01-01

The aim of this study was to select examples of mineral deposits and their weathering environment, showing the long-term behaviour, in geological time, measuring (area, volume) some constituent elements of radio-active waste storage subject to the hazards of hydrogeochemical weathering. Initially, a feasibility study was made to collate data available within the BRGM (mining group and public service) and from literature dealing with weathering of deposits. It was thus discovered that the analogy between radio-active waste storage and mineral deposits could be approached in two different yet complementary ways: - one approach is to observe the behaviour of a mineral deposit in relation to the country rocks. For this a bibliographic metallogenic study was made. The other approach is to observe the behaviour of chemical elements during deposition of a mineral deposit whose genesis is similar to the spatial and thermal environment of a deposit of radio-active waste in a geological formation. For this two sites were selected corresponding to hydrothermal systems showing strong analogies to those expected in the neighbourhood of the storage sites. These two sites, Langenberg in the Vosges and La Telhaie in Brittany, were the subject of complementary analytical work [fr

Topographic imprint on chemical weathering in deeply weathered soil-mantled landscapes (southern Brazil)

Science.gov (United States)

Vanacker, Veerle; Schoonejans, Jerome; Ameijeiras-Marino, Yolanda; Opfergelt, Sophie; Minella, Jean

2017-04-01

The regolith mantle is defined as the thin layer of unconsolidated material overlaying bedrock that contributes to shape the Earth's surface. The development of the regolith mantle in a landscape is the result of in-situ weathering, atmospheric input and downhill transport of weathering products. Bedrock weathering - the physical and chemical transformations of rock to soil - contributes to the vertical development of the regolith layer through downward propagation of the weathering front. Lateral transport of soil particles, aggregates and solutes by diffusive and concentrated particle and solute fluxes result in lateral redistribution of weathering products over the hillslope. In this study, we aim to expand the empirical basis on long-term soil evolution at the landscape scale through a detailed study of soil weathering in subtropical soils. Spatial variability in chemical mass fluxes and weathering intensity were studied along two toposequences with similar climate, lithology and vegetation but different slope morphology. This allowed us to isolate the topographic imprint on chemical weathering and soil development. The toposequences have convexo-concave slope morphology, and eight regolith profiles were analysed involving the flat upslope, steep midslope and flat toeslope part. Our data show a clear topographic imprint on soil development. Along hillslope, the chemical weathering intensity of the regolith profiles increases with distance from the crest. In contrast to the upslope positions, the soils in the basal concavities develop on in-situ and transported regolith. While the chemical weathering extent on the slope convexities (the upslope profiles) is similar for the steep and gentle toposequence, there is a clear difference in the rate of increase of the chemical weathering extent with distance from the crest. The increase of chemical weathering extent along hillslope is highest for the steep toposequence, suggesting that topography enhances soil particle

Mechanisms for chemostatic behavior in catchments: implications for CO2 consumption by mineral weathering

Science.gov (United States)

Clow, David W.; Mast, M. Alisa

2010-01-01

Concentrations of weathering products in streams often show relatively little variation compared to changes in discharge, both at event and annual scales. In this study, several hypothesized mechanisms for this “chemostatic behavior” were evaluated, and the potential for those mechanisms to influence relations between climate, weathering fluxes, and CO2 consumption via mineral weathering was assessed. Data from Loch Vale, an alpine catchment in the Colorado Rocky Mountains, indicates that cation exchange and seasonal precipitation and dissolution of amorphous or poorly crystalline aluminosilicates are important processes that help regulate solute concentrations in the stream; however, those processes have no direct effect on CO2 consumption in catchments. Hydrograph separation analyses indicate that old water stored in the subsurface over the winter accounts for about one-quarter of annual streamflow, and almost one-half of annual fluxes of Na and SiO2 in the stream; thus, flushing of old water by new water (snowmelt) is an important component of chemostatic behavior. Hydrologic flushing of subsurface materials further induces chemostatic behavior by reducing mineral saturation indices and increasing reactive mineral surface area, which stimulate mineral weathering rates. CO2 consumption by carbonic acid mediated mineral weathering was quantified using mass-balance calculations; results indicated that silicate mineral weathering was responsible for approximately two-thirds of annual CO2 consumption, and carbonate weathering was responsible for the remaining one-third. CO2 consumption was strongly dependent on annual precipitation and temperature; these relations were captured in a simple statistical model that accounted for 71% of the annual variation in CO2 consumption via mineral weathering in Loch Vale.

Chemical weathering and loess inputs to soils in New Zealand's Wairarapa region

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Lukens, C. E.; Norton, K. P.

2017-12-01

fluxes are remarkably low in these soils, which sit atop fractured graywacke that likely contributes very few weatherable primary minerals. The significant loess flux in this region may have important implications for estimates of total denudation and soil production, and must be accounted for to determine patterns in chemical weathering.

Chemical and Biological Catalytic Enhancement of Weathering of Silicate Minerals and industrial wastes as a Novel Carbon Capture and Storage Technology

Science.gov (United States)

Park, A. H. A.

2014-12-01

Increasing concentration of CO2 in the atmosphere is attributed to rising consumption of fossil fuels around the world. The development of solutions to reduce CO2 emissions to the atmosphere is one of the most urgent needs of today's society. One of the most stable and long-term solutions for storing CO2 is via carbon mineralization, where minerals containing metal oxides of Ca or Mg are reacted with CO2 to produce thermodynamically stable Ca- and Mg-carbonates that are insoluble in water. Carbon mineralization can be carried out in-situ or ex-situ. In the case of in-situ mineralization, the degree of carbonation is thought to be limited by both mineral dissolution and carbonate precipitation reaction kinetics, and must be well understood to predict the ultimate fate of CO2 within geological reservoirs. While the kinetics of in-situ mineral trapping via carbonation is naturally slow, it can be enhanced at high temperature and high partial pressure of CO2. The addition of weak organic acids produced from food waste has also been shown to enhance mineral weathering kinetics. In the case of the ex-situ carbon mineralization, the role of these ligand-bearing organic acids can be further amplified for silicate mineral dissolution. Unfortunately, high mineral dissolution rates often lead to the formation of a silica-rich passivation layer on the surface of silicate minerals. Thus, the use of novel solvent mixture that allows chemically catalyzed removal of this passivation layer during enhanced Mg-leaching surface reaction has been proposed and demonstrated. Furthermore, an engineered biological catalyst, carbonic anhydrase, has been developed and evaluated to accelerate the hydration of CO2, which is another potentially rate-limiting step of the carbonation reaction. The development of these novel catalytic reaction schemes has significantly improved the overall efficiency and sustainability of in-situ and ex-situ mineral carbonation technologies and allowed direct

Radionuclide Incorporation in Secondary Crystalline Minerals Resulting from Chemical Weathering of Selected Waste Glasses: Progress Report: Task kd.5b

International Nuclear Information System (INIS)

Mattigod, Shas V.; Serne, R. Jeffrey; Legore, Virginia L.; Parker, Kent E.; Orr, Robert D.; McCready, David E.; )

2003-01-01

Experiments were conducted by Pacific Northwest National Laboratory to evaluate potential incorporation of radionuclides in secondary mineral phases that form from weathering vitrified nuclear waste glasses. These experiments were conducted as part of the Immobilized Low-Activity Waste-Performance Assessment (ILAW-PA) to generate data on radionuclide mobilization and transport in a near-field environment of disposed vitrified wastes. The results of these experiments demonstrated that radionuclide sequestration can be significantly enhanced by promoting the formation of cage structured minerals such as sodalite from weathering glasses. These results have important implications regarding radionuclide sequestration/mobilization aspects that are not currently accounted for in the ILAW PA. Additional studies are required to confirm the results and to develop an improved understanding of the mechanisms of sequestration of radionuclides into the secondary and tertiary weathering products o f the ILAW glass to help refine how contaminants are released from the near-field disposal region out into the accessible environment. Of particular interest is to determine whether the contaminants remain sequestered in the glass weathering products for hundreds to thousands of years. If the sequestration can be shown to continue for long periods, another immobilization process can be added to the PA analysis and predicted risks should be lower than past predictions

Water geochemistry of the Xijiang basin rivers, South China: Chemical weathering and CO2 consumption

International Nuclear Information System (INIS)

Xu Zhifang; Liu Congqiang

2010-01-01

Research highlights: → The Xijiang River is the second largest river in China and flows through a large carbonate rock region in South China. → Sulfuric acid, which emanate from acid precipitation and the oxidation of sulfide minerals, is involved as a proton donor in weathering reactions in the Xijiang basin. → Calculated results show that the contribution of cations from rock weathering induced by sulfuric acid accounts for approximately 11.2%. → The flux of CO 2 released into the atmosphere is approximately 0.41 x 10 12 gC yr -1 produced by sulfuric acid-induced carbonate weathering in the Xijiang basin. → Sulfuric acid-induced carbonate weathering could counterbalance a significant part of the CO 2 consumed by silicate weathering. - Abstract: The Xijiang River, the mainstream of the Zhujiang (Pearl) River, which is the second largest river in China in terms of discharge, flows through a large carbonate rock region in South China. The chemical and Sr isotopic compositions of the Xijiang waters were determined during the high-flow season in order to understand the chemical weathering processes, associated CO 2 consumption and anthropogenic influences within the carbonate-dominated basin. The major ion compositions of the river waters are characterized by the dominance of Ca 2+ , Mg 2+ , HCO 3 - and are significantly rich in SO 4 2- . The SO 4 2- is mainly derived from the oxidation of sulfide minerals and acid precipitation caused by coal combustion. Chemical and Sr isotopic compositions of the river waters indicate that four reservoirs (carbonates, silicates, evaporites and anthropogenic inputs) contribute to the total dissolved loads. The chemical weathering rates of carbonates and silicates for the Xijiang basin are estimated to be approximately 78.5 and 7.45 ton km -2 a -1 , respectively. The total chemical weathering rate of rocks for the Xijiang basin is approximately 86.1 ton km -2 a -1 or 42 mm ka -1 , which is much higher than global mean

Variation of lithium isotope geochemistry during basalt weathering and secondary mineral transformations in Hawaii

Science.gov (United States)

Ryu, Jong-Sik; Vigier, Nathalie; Lee, Sin-Woo; Lee, Kwang-Sik; Chadwick, Oliver A.

2014-11-01

Lithium isotopes are a potential tracer of silicate weathering but the relationship between lithium isotope compositions and weathering state still need to be established with precision. Here, we report Li concentrations and Li isotope compositions of soils developed along a 4 million year humid-environment chronosequence in the Hawaiian Islands. Li concentrations are variable with depth and age, ranging from 0.24 to 21.3 ppm, and significant Li depletions (up to 92%) relative to parent basalts are systematically enhanced towards the surface. Our calculations show that the relative contribution from atmospheric deposits to the Li soil budget remains small, with a maximum contribution from dust Li of 20% at the oldest site. This is explained by the capacity of the weathering products to retain, within the profiles, the Li coming from basalt alteration, and allows us to explore more specifically the role of alteration processes on soil Li isotope signatures. The δ7Li values display a large range between -2.5‰ and +13.9‰. The youngest soils (0.3 ka) display the same δ7Li value as fresh basalt, regardless of depth, despite ∼30% Li loss by leaching, indicating that there is little Li isotope fractionation during the incipient stage of weathering. δ7Li values for the older soils (⩾20 ka) vary non-linearly as a function of time and can be explained by progressive mineral transformations starting with the synthesis of metastable short-range order (nano-crystalline) minerals and followed by their transformation into relatively inert secondary minerals. Results highlight significant Li isotope fractionation during secondary mineral formation and in particular during Li uptake by kaolinite. Finally, we suggest that the non-monotonous evolution of the regolith δ7Li value over the last 4 Ma is consistent with climatic variations, where congruent release of Li isotopes occurs during warmer periods.

Impact of grain size and rock composition on simulated rock weathering

Science.gov (United States)

Israeli, Yoni; Emmanuel, Simon

2018-05-01

Both chemical and mechanical processes act together to control the weathering rate of rocks. In rocks with micrometer size grains, enhanced dissolution at grain boundaries has been observed to cause the mechanical detachment of particles. However, it remains unclear how important this effect is in rocks with larger grains, and how the overall weathering rate is influenced by the proportion of high- and low-reactivity mineral phases. Here, we use a numerical model to assess the effect of grain size on chemical weathering and chemo-mechanical grain detachment. Our model shows that as grain size increases, the weathering rate initially decreases; however, beyond a critical size no significant decrease in the rate is observed. This transition occurs when the density of reactive boundaries is less than ˜ 20 % of the entire domain. In addition, we examined the weathering rates of rocks containing different proportions of high- and low-reactivity minerals. We found that as the proportion of low-reactivity minerals increases, the weathering rate decreases nonlinearly. These simulations indicate that for all compositions, grain detachment contributes more than 36 % to the overall weathering rate, with a maximum of ˜ 50 % when high- and low-reactivity minerals are equally abundant in the rock. This occurs because selective dissolution of the high-reactivity minerals creates large clusters of low-reactivity minerals, which then become detached. Our results demonstrate that the balance between chemical and mechanical processes can create complex and nonlinear relationships between the weathering rate and lithology.

Typhoon impacts on chemical weathering source provenance of a High Standing Island watershed, Taiwan

Science.gov (United States)

Meyer, Kevin J.; Carey, Anne E.; You, Chen-Feng

2017-10-01

Chemical weathering source provenance changes associated with Typhoon Mindulle (2004) were identified for the Choshui River Watershed in west-central Taiwan using radiogenic Sr isotope (87Sr/86Sr) and major ion chemistry analysis of water samples collected before, during, and following the storm event. Storm water sampling over 72 h was conducted in 3 h intervals, allowing for novel insight into weathering regime changes in response to intense rainfall events. Chemical weathering sources were determined to be bulk silicate and disseminated carbonate minerals at the surface and silicate contributions from deep thermal waters. Loss on ignition analysis of collected rock samples indicate disseminated carbonate can compose over 25% by weight of surface mineralogy, but typically makes up ∼2-3% of watershed rock. 87Sr/86Sr and major element molar ratios indicate that Typhoon Mindulle caused a weathering regime switch from normal flow incorporating a deep thermal signature to that of a system dominated by surface weathering. The data suggest release of silicate solute rich soil pore waters during storm events, creating a greater relative contribution of silicate weathering to the solute load during periods of increased precipitation and runoff. Partial depletion of this soil solute reservoir and possible erosion enhanced carbonate weathering lead to increased importance of carbonates to the weathering regime as the storm continues. Major ion data indicate that complex mica weathering (muscovite, biotite, illite, chlorite) may represent an important silicate weathering pathway in the watershed. Deep thermal waters represent an important contribution to river solutes during normal non-storm flow conditions. Sulfuric acid sourced from pyrite weathering is likely a major weathering agent in the Choshui River watershed.

Mechanism and kinetics of mineral weathering under acid conditions

NARCIS (Netherlands)

Anbeek, C.

1994-01-01

This study deals with the relationships between crystal structure, grain diameter, surface morphology and dissolution kinetics for feldspar and quartz under acid conditions.

Intensively ground samples from large, naturally weathered mineral fragments are frequently used in

Evolution of porosity and diffusivity associated with chemical weathering of a basalt clast

Energy Technology Data Exchange (ETDEWEB)

Navarre-Sitchler, A.; Steefel, C.I.; Yang, L.; Tomutsa, L.; Brantley, S.L.

2009-02-15

Weathering of rocks as a result of exposure to water and the atmosphere can cause significant changes in their chemistry and porosity. In low-porosity rocks, such as basalts, changes in porosity, resulting from chemical weathering, are likely to modify the rock's effective diffusivity and permeability, affecting the rate of solute transport and thus potentially the rate of overall weathering to the extent that transport is the rate limiting step. Changes in total porosity as a result of mineral dissolution and precipitation have typically been used to calculate effective diffusion coefficients through Archie's law for reactive transport simulations of chemical weathering, but this approach fails to account for unconnected porosity that does not contribute to transport. In this study, we combine synchrotron X-ray microcomputed tomography ({mu}CT) and laboratory and numerical diffusion experiments to examine changes in both total and effective porosity and effective diffusion coefficients across a weathering interface in a weathered basalt clast from Costa Rica. The {mu}CT data indicate that below a critical value of {approx}9%, the porosity is largely unconnected in the basalt clast. The {mu}CT data were further used to construct a numerical pore network model to determine upscaled, effective diffusivities as a function of total porosity (ranging from 3 to 30%) for comparison with diffusivities determined in laboratory tracer experiments. By using effective porosity as the scaling parameter and accounting for critical porosity, a model is developed that accurately predicts continuum-scale effective diffusivities across the weathering interface of the basalt clast.

Chemical weathering as a mechanism for the climatic control of bedrock river incision

Science.gov (United States)

Murphy, Brendan P.; Johnson, Joel P. L.; Gasparini, Nicole M.; Sklar, Leonard S.

2016-04-01

Feedbacks between climate, erosion and tectonics influence the rates of chemical weathering reactions, which can consume atmospheric CO2 and modulate global climate. However, quantitative predictions for the coupling of these feedbacks are limited because the specific mechanisms by which climate controls erosion are poorly understood. Here we show that climate-dependent chemical weathering controls the erodibility of bedrock-floored rivers across a rainfall gradient on the Big Island of Hawai‘i. Field data demonstrate that the physical strength of bedrock in streambeds varies with the degree of chemical weathering, which increases systematically with local rainfall rate. We find that incorporating the quantified relationships between local rainfall and erodibility into a commonly used river incision model is necessary to predict the rates and patterns of downcutting of these rivers. In contrast to using only precipitation-dependent river discharge to explain the climatic control of bedrock river incision, the mechanism of chemical weathering can explain strong coupling between local climate and river incision.

Geochemical and mineralogical study of selected weathered samples from Olkiluoto site

International Nuclear Information System (INIS)

Lindberg, A.

2009-02-01

Optical microscopy, chemical analyses and X-ray diffraction method were used to study the influence of weathering from 11 drill core samples from shallow depths (< 25 m). The samples, 4 to 22 cm in length were drilled from Olkiluoto study site, Eurajoki, and they represent the common rock types of local bedrock: mica gneiss, tonalitic and granodioritic gneiss. Two of the samples were macroscopically unweathered and 9 of them were remarkably altered. The alteration was shown as porosity, the abundance of chlorite instead of biotite and pink, unclear feldspars. Many samples also contained red-brown hematite and fractures, some of them coated with secondary minerals, even clay. Microscopically the most visible feature of weathering was the total alteration of plagioclase and cordierite to sericite. In many samples also biotite was richly altered to chlorite and opaque minerals. Microfractures were common and they were filled by hematite, kaolinite and fine-grained muscovite (sericite). Hematite was, in some cases, also largely replacing the weathered minerals, feldspars and cordierite. Chemical alteration was not clear, because the alteration of main minerals have produced secondary minerals with almost the same chemical composition without any reasonable depleting or enrichment of certain elements. X-ray diffraction determination of samples proved, that often plagioclase was replaced by mica and biotite by chlorite. In some cases the samples contained products of chemical weathering, kaolinite and smectite. (orig.)

Mineral weathering in acid saprolites from subtropical, southern Brazil Intemperismo subtropical de minerais em saprolitos ácidos do Sul do Brasil

Directory of Open Access Journals (Sweden)

Celso Augusto Clemente

2007-12-01

Full Text Available Because weathering of minerals releases chemical elements into the biogeochemical cycle, characterization of their weathering products helps to better model groundwater quality, formation of secondary minerals and nutrient flux through the trophic chain. Based on microscopic and elemental analyses, weathering of riodacite from Serra Geral formation was characterized and weathering paths proposed. Three weathering paths of plagioclase phenocrystals were identified: plagioclase to gibbsite (Pg1; plagioclase to gels and gibbsite (Pg2; and plagioclase to gels, gibbsite and kaolinite (Pg3. Pyroxenes weathered to smectite and goethite (Py1, or to goethite and gibbsite (Py2, and magnetite weathered directly into iron oxides. Rock matrix comprises 90% of rock volume, and weathered to kaolinite and gibbsite, which explains why these minerals were the most abundant in the weathering products of these saprolites.O intemperismo de minerais primários disponibiliza elementos químicos no ciclo biogeoquímico, que por sua vez influencia a qualidade da água subterrânea, formação de minerais secundários e o fluxo de nutrientes na cadeia trófica. Com base na análise microscópica e elemental, o intemperismo de riodacito da formação Serra Geral foi caracterizado e mecanismos de intemperismo propostos. Três processos principais de intemperismo de fenocristais de plagioclásios foram identificados: plagioclásio para gibbsita (Pg1; plagioclásio para gel e gibbsita (Pg2, e plagioclásio para gel, gibbsita e caulinita (Pg3. Piroxênios intemperizaram-se para esmectita e goetita (Py1, ou para goethita e gibbsita (Py2, e magnetita intemperizou-se para óxidos de ferro. A matriz da rocha compõe 90% do volume total, e intemperiza-se para caulinita e gibbsita, o que explica a abundância destes minerais nos produtos de intemperismo destes saprolitos.

Fossil Microorganisms and Formation of Early Precambrian Weathering Profiles

Science.gov (United States)

Rozanov, A. Yu; Astafieva, M. M.; Vrevsky, A. B.; Alfimova, N. A.; Matrenichev, V. A.; Hoover, R. B.

2009-01-01

Weathering crusts are the only reliable evidences of the existence of continental conditions. Often they are the only source of information about exogenous processes and subsequently about conditions under which the development of the biosphere occurred. A complex of diverse fossil microorganisms was discovered as a result of Scanning Electron Microscope investigations. The chemical composition of the discovered fossils is identical to that of the host rocks and is represented by Si, Al, Fe, Ca and Mg. Probably, the microorganisms fixed in rocks played the role of catalyst. The decomposition of minerals comprising the rocks and their transformation into clayey (argillaceous) minerals, most likely occurred under the influence of microorganisms. And may be unique weathering crusts of Early Precambrian were formed due to interaction between specific composition of microorganism assemblage and conditions of hypergene transformations. So it is possible to speak about colonization of land by microbes already at that time and about existence of single raw from weathering crusts (Primitive soils) to real soils.

Chemical dispersibility testing of fresh and weathered oils

International Nuclear Information System (INIS)

Brandvik, P.J.; Daling, P.S.; Aareskjold, K.

1991-05-01

This activity in the DIspersants on Weathered Oils-project (DIWO) is a continuation and an extended study of the dispersibility study described in DIWO report No. 3. The main objective has been to study the chemical dispersibility of fresh and weathered oils produced or transported in Norwegian waters. Other important aims of this study have been: To correlate the effectiveness results obtained by three different laboratory methods; to determine the relationship between the dispersant effectiveness and the change in the oils' physico-chemical properties due to weathering (topping, photo-oxidation and w/o-emulsification). This study has been performed with 8 different oil types and 12 different weathering degrees of each oil type. The work performed clearly demonstrates that the oil type and especially the weathering properties are essential for the performance of dispersants at sea. 41 figs., 5 tabs., 16 refs

Forest soil mineral weathering rates: use of multiple approaches

Science.gov (United States)

Randy K. Kolka; D.F. Grigal; E.A. Nater

1996-01-01

Knowledge of rates of release of base cations from mineral dissolution (weathering) is essential to understand ecosystem elemental cycling. Although much studied, rates remain enigmatic. We compared the results of four methods to determine cation (Ca + Mg + K) release rates at five forested soils/sites in the northcentral U.S.A. Our premise was that multiple...

Mineral weathering experiments to explore the effects of vegetation shifts in high mountain region (Wind River Range, Wyoming, USA)

Science.gov (United States)

Mavris, Christian; Furrer, Gerhard; Dahms, Dennis; Anderson, Suzanne P.; Blum, Alex; Goetze, Jens; Wells, Aaron; Egli, Markus

2015-04-01

Climate change influences the evolution of soil and landscape. With changing climate, both flora and fauna must adapt to new conditions. It is unknown in many respects to what extent soils will react to warming and vegetation change. The aim of this study was to identify possible consequences for soils in a dry-alpine region with respect to weathering of primary minerals and leaching of elements under expected warming climate conditions due to shifts in vegetation. To achieve this, a field empirical approach was used in combination with laboratory weathering experiments simulating several scenarios. Study sites located in Sinks Canyon and in Stough Basin of the Wind River Range, Wyoming, USA, encompass ecotones that consist of tundra, forest, or sagebrush (from moist to dry, with increasing temperature, respectively). All soils are developed on granitoid moraines. The mineralogy of the soils along the altitudinal sequence was analysed using cathodoluminescence and X-ray diffraction, and revealed clear mineral transformations: biotite and plagioclase were both weathered to smectite while plagioclase also weathered to kaolinite. Cooler, wetter, altitude-dependent conditions seemed to promote weathering of these primary minerals. To test the impact of soil solutions from different ecotones on mineral weathering, aqueous extracts from topsoils (A horizons) were reacted with subsoils (B horizons) in batch experiments. Aqueous extracts of topsoil samples were generated for all three ecotones, and these solutions were characterized. For the batch experiments, the topsoil extracts were reacted for 1800 hours with the subsoil samples of the same ecotone, or with the subsoil samples from higher altitude ecotones. Solutions collected periodically during the experiments were measured using ICP-OES and ion chromatography. Dissolved Ca, Mg and K were mainly controlled by the chemical weathering of oligoclase, K-feldspar and biotite. With increasing altitude (and consequently

Climatic control on clay mineral formation

Indian Academy of Sciences (India)

Many physico-chemical variables like rock-type,climate,topography and exposure age affect weathering environments.In the present study,an attempt is made to understand how the nature of clay minerals formed due to weathering differs in tropical regions receiving high and low rainfall. Clay mineralogy of weathering pro ...

Process-based modeling of silicate mineral weathering responses to increasing atmospheric CO2 and climate change

Science.gov (United States)

Banwart, Steven A.; Berg, Astrid; Beerling, David J.

2009-12-01

A mathematical model describes silicate mineral weathering processes in modern soils located in the boreal coniferous region of northern Europe. The process model results demonstrate a stabilizing biological feedback mechanism between atmospheric CO2 levels and silicate weathering rates as is generally postulated for atmospheric evolution. The process model feedback response agrees within a factor of 2 of that calculated by a weathering feedback function of the type generally employed in global geochemical carbon cycle models of the Earth's Phanerozoic CO2 history. Sensitivity analysis of parameter values in the process model provides insight into the key mechanisms that influence the strength of the biological feedback to weathering. First, the process model accounts for the alkalinity released by weathering, whereby its acceleration stabilizes pH at values that are higher than expected. Although the process model yields faster weathering with increasing temperature, because of activation energy effects on mineral dissolution kinetics at warmer temperature, the mineral dissolution rate laws utilized in the process model also result in lower dissolution rates at higher pH values. Hence, as dissolution rates increase under warmer conditions, more alkalinity is released by the weathering reaction, helping maintain higher pH values thus stabilizing the weathering rate. Second, the process model yields a relatively low sensitivity of soil pH to increasing plant productivity. This is due to more rapid decomposition of dissolved organic carbon (DOC) under warmer conditions. Because DOC fluxes strongly influence the soil water proton balance and pH, this increased decomposition rate dampens the feedback between productivity and weathering. The process model is most sensitive to parameters reflecting soil structure; depth, porosity, and water content. This suggests that the role of biota to influence these characteristics of the weathering profile is as important, if not

Constitutive mass balance relations between chemical composition, volume, density, porosity, and strain in metasomatic hydrochemical systems: Results on weathering and pedogenesis

Science.gov (United States)

Brimhall, George H.; Dietrich, William E.

1987-03-01

Relations characterizing the chemical, physical, and mechanical changes resulting from metasomatic hydrochemical processes are developed using mass balance models which formally link chemical composition to bulk density, mineral density, volumetric properties, porosity, and amount of deformation (strain). Rigorous analysis of aqueous solute transport effects is then made possible in a variety of porous media flow environments including chemical weathering, pedogenesis (soil formation), diagenesis, ore deposition and enrichment, and metamorphism. Application of these linear constitutive relations to chemical weathering profiles shows that immobile and locally mobile chemical elements, with masses conserved on the scale of soil profiles, can be accurately identified from analysis of appropriate data arrays and then used as natural geochemical tracers to infer the nature and extent of hydrochemical weathering processes and volume changes during pedogenesis. Assumptions commonly made in the past about the supposed immobility of certain elements, e.g., Ti and Zr, become unnecessary. Quantitative differentiation between the effects of residual and supergene fractionation is then easily made. These methods are applied to Ni-rich laterites developed by weathering of ultramafic rocks, showing that during ordinary residual enrichment, Ni is concentrated by as much as 4× protolith peridotite concentrations. This occurs simply by silicate mineral dissolution and removal of chemical elements other than Ni ( e.g., Mg) with a corresponding reduction in saprolite density and increase in bulk porosity without significant deformation. In contrast, laterites with mineable concentrations of Ni which are similarly undeformed (such as the Nickel Mountain Mine in Riddle, Oregon) have experienced, in addition to residual enrichment, strong supergene enrichment by fractionation of ore elements between a leached zone from which Ni is extracted and a complementary enriched zone positioned

Chemical and Physical Weathering of Granites in a Semi-Arid Savanna

Science.gov (United States)

Khomo, L.; Hartshorn, A.; Chadwick, O.; Kurtz, A.; Heimsath, A.; Rogers, K.

2005-12-01

The catena concept describes soil properties on hillslopes and implies a hydrological mass redistribution process that has been applied differently in different parts of the Earth. In tectonically active regions, it is mostly used to describe the redistribution of mass by overland flow leading to thickening soil mantles downslope. This application is somewhat different from its initial and still popular usage in tectonically inactive areas of Africa, where it defines long-term soil property differentiation along hillslopes as controlled by internal soil hydrology as opposed to overland flow. Many ecologists have found the "African" catena concept to be useful as an organizing principal for savanna studies, but there has been little recent research on catenas per se in Africa. Elsewhere however, there is a growing body of research that places the concept ever more strongly into a landscape evolution context. Here, we apply these new approaches to catenas in a South African savanna underlain by a heterogeneous suite of Basement granites straddling a gradient in effective precipitation. We constrain the weathering extent of hilly terrains formed on these oldrocks by calculating element losses with solid-phase mass-balance calculations augmented by cosmogenic (26Al/10Be) derived rates of landscape denudation. We test the efficacy of Ti, Zr and Nb as immobile elements to benchmark chemical losses and gains in these semi-arid weathering environments. We also trace and quantify the abundance of the host minerals for these elements (Ti = rutile and ilmenite, Nb = columbite and Zr = zircon and baddleyite) in a variety of rocks in the basement complex. This analysis provides the boundary conditions for assigning immobile elements to parent materials required for the mass balance calculations. We calculate total denudation using the cosmogenic isotopes and then partition it into chemical and physical loss vectors using the mass balance calculations for representative

Natural weathering in dry disposed ash dump: Insight from chemical, mineralogical and geochemical analysis of fresh and unsaturated drilled cores.

Science.gov (United States)

Akinyemi, S A; Akinlua, A; Gitari, W M; Khuse, N; Eze, P; Akinyeye, R O; Petrik, L F

2012-07-15

Some existing alternative applications of coal fly ash such as cement manufacturing; road construction; landfill; and concrete and waste stabilisation use fresh ash directly collected from coal-fired power generating stations. Thus, if the rate of usage continues, the demand for fresh ash for various applications will exceed supply and use of weathered dry disposed ash will become necessary alternative. As a result it's imperative to understand the chemistry and pH behaviour of some metals inherent in dry disposed fly ash. The bulk chemical composition as determined by XRF analysis showed that SiO2, Al2O3 and Fe2O3 were the major oxides in fresh ash and unsaturated weathered ashes. The unsaturated weathered ashes are relatively depleted in CaO, Fe2O3, TiO2, SiO2, Na2O and P2O5 due to dissolution and hydrolysis caused by chemical interaction with ingressing CO2 from the atmosphere and infiltrating rain water. Observed accumulations of Fe2O3, TiO2, CaO, K2O, Na2O and SO3 and Zn, Zr, Sr, Pb, Ni, Cr and Co in the lower layers indicate progressive downward movement through the ash dump though at a slow rate. The bulk mineralogy of unsaturated weathered dry disposed ash, as determined by XRD analysis, revealed quartz and mullite as the major crystalline phases; while anorthite, hematite, enstatite, lime, calcite, and mica were present as minor mineral phases. Pore water chemistry revealed a low concentration of readily soluble metals in unsaturated weathered ashes in comparison with fresh ash, which shows high leachability. This suggests that over time the precipitation of transient minor secondary mineral phases; such as calcite and mica might retard residual metal release from unsaturated weathered ash. Chloride and sulphate species of the water soluble extracts of weathered ash are at equilibrium with Na+ and K+; these demonstrate progressive leaching over time and become supersaturated at the base of unsaturated weathered ash. This suggests that the ash dump does not

A Reactive Transport Model for Marcellus Shale Weathering

Science.gov (United States)

Li, L.; Heidari, P.; Jin, L.; Williams, J.; Brantley, S.

2017-12-01

Shale formations account for 25% of the land surface globally. One of the most productive shale-gas formations is the Marcellus, a black shale that is rich in organic matter and pyrite. As a first step toward understanding how Marcellus shale interacts with water, we developed a reactive transport model to simulate shale weathering under ambient temperature and pressure conditions, constrained by soil chemistry and water data. The simulation was carried out for 10,000 years, assuming bedrock weathering and soil genesis began right after the last glacial maximum. Results indicate weathering was initiated by pyrite dissolution for the first 1,000 years, leading to low pH and enhanced dissolution of chlorite and precipitation of iron hydroxides. After pyrite depletion, chlorite dissolved slowly, primarily facilitated by the presence of CO2 and organic acids, forming vermiculite as a secondary mineral. A sensitivity analysis indicated that the most important controls on weathering include the presence of reactive gases (CO2 and O2), specific surface area, and flow velocity of infiltrating meteoric water. The soil chemistry and mineralogy data could not be reproduced without including the reactive gases. For example, pyrite remained in the soil even after 10,000 years if O2 was not continuously present in the soil column; likewise, chlorite remained abundant and porosity remained small with the presence of soil CO2. The field observations were only simulated successfully when the specific surface areas of the reactive minerals were 1-3 orders of magnitude smaller than surface area values measured for powdered minerals, reflecting the lack of accessibility of fluids to mineral surfaces and potential surface coating. An increase in the water infiltration rate enhanced weathering by removing dissolution products and maintaining far-from-equilibrium conditions. We conclude that availability of reactive surface area and transport of H2O and gases are the most important

A review of operational, regional-scale, chemical weather forecasting models in Europe

Directory of Open Access Journals (Sweden)

J. Kukkonen

2012-01-01

Full Text Available Numerical models that combine weather forecasting and atmospheric chemistry are here referred to as chemical weather forecasting models. Eighteen operational chemical weather forecasting models on regional and continental scales in Europe are described and compared in this article. Topics discussed in this article include how weather forecasting and atmospheric chemistry models are integrated into chemical weather forecasting systems, how physical processes are incorporated into the models through parameterization schemes, how the model architecture affects the predicted variables, and how air chemistry and aerosol processes are formulated. In addition, we discuss sensitivity analysis and evaluation of the models, user operational requirements, such as model availability and documentation, and output availability and dissemination. In this manner, this article allows for the evaluation of the relative strengths and weaknesses of the various modelling systems and modelling approaches. Finally, this article highlights the most prominent gaps of knowledge for chemical weather forecasting models and suggests potential priorities for future research directions, for the following selected focus areas: emission inventories, the integration of numerical weather prediction and atmospheric chemical transport models, boundary conditions and nesting of models, data assimilation of the various chemical species, improved understanding and parameterization of physical processes, better evaluation of models against data and the construction of model ensembles.

Nitrogen fixation in lichens is important for improved rock weathering

Indian Academy of Sciences (India)

MADU

1996), suggesting that fungal acid production is altered in the lichen. Weathering .... 5019 biofilm, (vii) S. recemosum + B. elkanii SEMIA 5019 biofilm, and (viii) the .... chemical factors in soil mineral wethering; in Interactions of soil minerals with ...

Mesocosm-Scale Experimental Quantification of Plant-Fungi Associations on Carbon Fluxes and Mineral Weathering

Science.gov (United States)

Andrews, M. Y.; Palmer, B.; Leake, J. R.; Banwart, S. A.; Beerling, D. J.

2009-12-01

The rise of land plants in the Paleozoic is classically implicated as driving lower atmospheric CO2 levels through enhanced weathering of Ca and Mg bearing silicate minerals. However, this view overlooks the fact that plants coevolved with associated mycorrhizal fungi over this time, with many of the weathering processes usually ascribed to plants actually being driven by the combined activities of roots and mycorrhizal fungi. Here we present initial results from a novel mesocosm-scale laboratory experiment designed to allow investigation of plant-driven carbon flux and mineral weathering at different soil depths under ambient (400 ppm) and elevated (1500 ppm) atmospheric CO2. Four species of plants were chosen to address evolutionary trends in symbiotic mycorrhizal association and rooting depth on biologically driven silicate weathering under the different CO2 regimes. Gymnosperms were used to investigate potential differences in weathering capabilities of two fungal symbioses: Sequoia sempervirens and Metasequoia glyptostroboides (arbuscular mycorrhizal, AM) and Pinus sylvestris (ectomycorrhizal, EM), and the shallow rooted ancient fern, Osmunda regalis, used to provide a contrast to the three more deeply rooted trees. Plants were grown in a cylindrical mesocosm with four horizontal inserts at each depth. These inserts are a mesh-covered dual-core unit whereby an inner core containing silicate minerals can be rotated within an outer core. The mesh excludes roots from the cylinders allowing fungal-rock pairings to be examined at each depth. Each core contains either basalt or granite, each with severed (rotated cores) or intact (static cores) mycorrhizae. This system provides a unique opportunity to examine the ability of a plant to weather minerals with and without its symbiotic fungi. Preliminary results indicate marked differences in nutritional and water requirements, and response to elevated CO2 between the species. The bulk solution chemistries (p

Kinetically limited weathering at low denudation rates in semiarid climatic conditions

Science.gov (United States)

Schoonejans, Jérôme; Vanacker, Veerle; Opfergelt, Sophie; Ameijeiras-Mariño, Yolanda; Christl, Marcus

2016-02-01

Biogeochemical cycling within the Critical Zone depends on the interactions between minerals and fluids controlling chemical weathering and physical erosion rates. In this study, we explore the role of water availability in controlling soil chemical weathering in semiarid climatic conditions. Weathering rates and intensities were evaluated for nine soil profiles located on convex ridge crests of three mountain ranges in the Spanish Betic Cordillera. We combine a geochemical mass balance with 10Be cosmogenic nuclides to constrain chemical weathering intensities and long-term denudation rates. As such, this study presents new data on chemical weathering and 10Be-derived denudation for understudied semiarid climate systems. In the Betic Cordillera, chemical weathering intensities are relatively low (~5 to 30% of the total denudation of the soil) and negatively correlated with the magnitude of the water deficit in soils. Chemical mass losses are inversely related to denudation rates (14-109 mm/kyr) and positively to soil thickness (14-58 cm); these results are consistent with kinetic limitation of chemical weathering rates. A worldwide compilation of chemical weathering data suggests that soil water balance may regulate the coupling between chemical weathering and physical erosion by modulating soil solute fluxes. Therefore, future landscape evolution models that seek to link chemical weathering and physical erosion should include soil water flux as an essential driver of weathering.

Coupling of physical erosion and chemical weathering after phases of intense human activity

Science.gov (United States)

Schoonejans, Jerome; Vanacker, Veerle; Opfergelt, Sophie; Ameijeiras-Mariño, Yolanda; Kubik, Peter W.

2014-05-01

Anthropogenic disturbance of natural vegetation profoundly alters the lateral and vertical fluxes of soil nutrients and particles at the land surface. Human-induced acceleration of soil erosion can thereby result in an imbalance between physical erosion, soil production and chemical weathering. The (de-)coupling between physical erosion and chemical weathering in ecosystems with strong anthropogenic disturbances is not yet fully understood, as earlier studies mostly focused on natural ecosystems. In this study, we explore the chemical weathering intensity for four study sites located in the Internal Zone of the Spanish Betic Cordillera. Most of the sites belong to the Nevado-Filabres complex, but are characterized by different rates of long-term exhumation, 10Be catchment-wide denudation and hill slope morphology. Denudation rates are generally low, but show large variation between the three sites (from 23 to 246 mm kyr-1). The magnitude of denudation rates is consistent with longer-term uplift rates derived from marine deposits, fission-track measurements and vertical fault slip rates. Two to three soil profiles were sampled per study site at exposed ridge tops. All soils overly fractured mica schist, and are very thin (< 60cm). In each soil profile, we sampled 5 depth slices, rock fragments and the (weathered) bedrock. In total, 38 soil and 20 rock samples were analyzed for their chemical composition. The chemical weathering intensity is constrained by the Chemical Depletion Fraction that is based on a chemical mass balance approach using Zr as an immobile element. Chemical weathering accounts for 5 to 35% of the total mass lost due to denudation. We observe systematically higher chemical weathering intensities (CDFs) in sites with lower denudation rates (and vice versa), suggesting that weathering is supply-limited. Our measurements of soil elemental losses from 10 soil profiles suggest that the observed variation in chemical weathering is strongly associated

Anthropogenically enhanced chemical weathering and carbon evasion in the Yangtze Basin

Science.gov (United States)

Guo, Jingheng; Wang, Fushun; Vogt, Rolf David; Zhang, Yuhang; Liu, Cong-Qiang

2015-01-01

Chemical weathering is a fundamental geochemical process regulating the atmosphere-land-ocean fluxes and earth’s climate. It is under natural conditions driven primarily by weak carbonic acid that originates from atmosphere CO2 or soil respiration. Chemical weathering is therefore assumed as positively coupled with its CO2 consumption in contemporary geochemistry. Strong acids (i.e. sulfuric- and nitric acid) from anthropogenic sources have been found to influence the weathering rate and CO2 consumption, but their integrated effects remain absent in the world largest river basins. By interpreting the water chemistry and overall proton budget in the Yangtze Basin, we found that anthropogenic acidification had enhanced the chemical weathering by 40% during the past three decades, leading to an increase of 30% in solute discharged to the ocean. Moreover, substitution of carbonic acid by strong acids increased inorganic carbon evasion, offsetting 30% of the CO2 consumption by carbonic weathering. Our assessments show that anthropogenic loadings of sulfuric and nitrogen compounds accelerate chemical weathering but lower its CO2 sequestration. These findings have significant relevance to improving our contemporary global biogeochemical budgets. PMID:26150000

Artificial Weathering of Biotite and Uranium Sorption Characteristics

International Nuclear Information System (INIS)

Lee, Seung Yeop; Baik, Min Hoon; Lee, Jae Kwang

2009-01-01

An experiment for uranium sorption onto fresh and weathered biotites was performed. After centrifugation, concentrations of uranium in the supernatants were analyzed using ICP-MS, and biotite samples were investigated using XRD and SEM. With powdered biotites (<3 mm in size), we have conducted uranium sorption experiments about fresh and weathered biotites to obtain uranium sorption amounts in various pH conditions. The uranium sorption was not high at a low pH (e.g., pH 3), but increased with increasing pH. There were lower uranium sorption by the weathered biotites than by the fresh ones, and the difference was much larger at higher pH (e.g., pH 11). The lower sorption values of uranium by the weathered biotites may be caused by a change of mineral surfaces and a chemical behavior of surrounding dissolved elements. It seems that the uranium-mineral interaction has been diminished, especially, in the weathered biotite by a destruction and dissolution of preferential sorption sites on the mineral surfaces and by the colloidal formation from dissolved elements.

Natural mineral waters: chemical characteristics and health effects

Science.gov (United States)

Quattrini, Sara; Pampaloni, Barbara; Brandi, Maria Luisa

2016-01-01

Summary Water contributes significantly to health and a daily intake of 1.5 to 2 liters of water should be guaranteed, because a good hydration is essential to maintain the body water equilibrium, although needs may vary among people. However, worldwide population is far from the Recommended Allowance for water intake. Among the waters for human uses, there are ‘waters (treated or not), intended for drinking, used for the food and beverages preparation or for other domestic purposes’ and natural mineral waters, that are ‘originated from an aquifer or underground reservoir, spring from one or more natural or bore sources and have specific hygienic features and, eventually, healthy properties’. According to the European Legislation (2009/54/EC Directive), physical and chemical characterization is used to make a classification of the different mineral waters, basing on the analysis of main parameters. Mineral composition enables to classify natural mineral waters as bicarbonate mineral waters, sulphate mineral waters, chloride mineral waters, calcic mineral waters, magnesiac mineral waters, fluorurate mineral waters, ferrous mineral waters and sodium-rich mineral waters. Although the concerns about bottled mineral waters (due to plasticizers and endocrine disruptors), many are the health effects of natural mineral waters and several studies explored their properties and their role in different physiological and pathological conditions. PMID:28228777

Weathering Profiles in Phosphorus-Rich Rocks at Gusev Crater, Mars, Suggest Dissolution of Phosphate Minerals into Potentially Habitable Near-Neutral Waters.

Science.gov (United States)

Adcock, Christopher T; Hausrath, Elisabeth M

2015-12-01

Abundant evidence indicates that significant surface and near-surface liquid water has existed on Mars in the past. Evaluating the potential for habitable environments on Mars requires an understanding of the chemical and physical conditions that prevailed in such aqueous environments. Among the geological features that may hold evidence of past environmental conditions on Mars are weathering profiles, such as those in the phosphorus-rich Wishstone-class rocks in Gusev Crater. The weathering profiles in these rocks indicate that a Ca-phosphate mineral has been lost during past aqueous interactions. The high phosphorus content of these rocks and potential release of phosphorus during aqueous interactions also make them of astrobiological interest, as phosphorus is among the elements required for all known life. In this work, we used Mars mission data, laboratory-derived kinetic and thermodynamic data, and data from terrestrial analogues, including phosphorus-rich basalts from Idaho, to model a conceptualized Wishstone-class rock using the reactive transport code CrunchFlow. Modeling results most consistent with the weathering profiles in Wishstone-class rocks suggest a combination of chemical and physical erosion and past aqueous interactions with near-neutral waters. The modeling results also indicate that multiple Ca-phosphate minerals are likely in Wishstone-class rocks, consistent with observations of martian meteorites. These findings suggest that Gusev Crater experienced a near-neutral phosphate-bearing aqueous environment that may have been conducive to life on Mars in the past. Mars-Gusev Crater-Wishstone-Reactive transport modeling-CrunchFlow-Aqueous interactions-Neutral pH-Habitability.

NATO Advanced Research Workshop on The Chemistry of Weathering

CERN Document Server

1985-01-01

Several important developments in our understanding of the chemistry of weathering have occurred in the last few years: 1. There has been a major breakthrough in our understanding of the mechanisms controlling the kinetics of sil icate dissolution, and there have been major advances in computer modeling of weathering processes. 2. There has been a growing recognition of the importance of organic solutes in the weathering process, and hence of the inter-relationships between mineral weathering and the terrestrial ecosystem. 3. The impact of acid deposition ("acid rain") has been widely recognized. The processes by which acid deposition is neutral ized are closely related to the processes of normal chemical weathering; an understanding of the chemistry of weathering is thus essential for predicting the effects of acid deposition. 4. More high-qual ity data have become available on the chemical dynamics of smal I watersheds and large river systems, which represent the integrated effects of chemical weathering.

Climatic control on clay mineral formation: Evidence from ...

Indian Academy of Sciences (India)

are the most important factors that determine kinetics of chemical weathering. Mineral alteration ... perature, pressure and microbial activity. Among various factors ... physical factor) and rainfall (a chemical factor). (Velde 1992, p. 118).

Isotopic chemical weathering behaviour of Pb derived from a high-Alpine Holocene lake-sediment record

Science.gov (United States)

Gutjahr, Marcus; Süfke, Finn; Gilli, Adrian; Anselmetti, Flavio; Glur, Lukas; Eisenhauer, Anton

2017-04-01

Several studies assessing the chemical weathering systematics of Pb isotopes provided evidence for the incongruent release of Pb from source rocks during early stages of chemical weathering, resulting in runoff compositions more radiogenic (higher) than the bulk source-rock composition [e.g. 1]. Deep NW Atlantic seawater Pb isotope records covering the last glacial-interglacial transition further support these findings. Clear excursions towards highly radiogenic Pb isotopic input in the deep NW Atlantic seen during the early Holocene, hence after the large-scale retreat of the Laurentide Ice Sheet in North America, are interpreted to be controlled by preferential release of radiogenic Pb from U- and Th-rich mineral phases during early stages of chemical weathering that are less resistant to chemical dissolution than other rock-forming mineral phases [2-4]. To date, however, no terrestrial Pb isotope record exists that could corroborate the evidence from deep marine sites for efficient late deglacial weathering and washout of radiogenic Pb. We present a high-resolution adsorbed Pb isotope record from a sediment core retrieved from Alpine Lake Grimsel (1908 m.a.s.l.) in Switzerland, consisting of 117 Pb compositions over the past 10 kyr. This high-Alpine study area is ideally located for incipient and prolonged chemical weathering studies. The method used to extract the adsorbed lake Pb isotope signal is identical to previous marine approaches targeting the authigenic Fe-Mn oxyhydroxides fraction within the lake sediments [5, 6]. The Pb isotope compositions are further accompanied by various elemental ratios derived from the same samples that equally trace climatic boundary conditions in the Grimsel Lake area. The Pb isotopic composition recorded in Lake Grimsel is remarkably constant throughout the majority of the Holocene until ˜2.5 ka BP, despite variable sediment composition and -age, and isotopically relatively close to the signature of the granitic source rock

Carbon mineralization and pyrite oxidation in groundwater: Importance for silicate weathering in boreal forest soils and stream base-flow chemistry

International Nuclear Information System (INIS)

Klaminder, J.; Grip, H.; Moerth, C.-M.; Laudon, H.

2011-01-01

Research highlights: → Organic compounds is mineralized during later transport in deep groundwater aquifers. → Carbonic acid generated by this process stimulates dissolution of silicate minerals. → Protons derived from pyrite oxidation also affects weathering in deep groundwater. → The identified weathering mechanisms affect base-flow chemistry in boreal streams. - Abstract: What role does mineralized organic C and sulfide oxidation play in weathering of silicate minerals in deep groundwater aquifers? In this study, how H 2 CO 3 , produced as a result of mineralization of organic matter during groundwater transport, affects silicate weathering in the saturated zone of the mineral soil along a 70 m-long boreal hillslope is demonstrated. Stream water measurements of base cations and δ 18 O are included to determine the importance of the deep groundwater system for downstream surface water. The results suggest that H 2 CO 3 generated from organic compounds being mineralized during the lateral transport stimulates weathering at depths between 0.5 and 3 m in the soil. This finding is indicated by progressively increasing concentrations of base cations-, silica- and inorganic C (IC) in the groundwater along the hillslope that co-occur with decreasing organic C (OC) concentrations. Protons derived from sulfide oxidation appear to be an additional driver of the weathering process as indicated by a build-up of SO 4 2- in the groundwater during lateral transport and a δ 34 S per mille value of +0.26-3.76 per mille in the deep groundwater indicating S inputs from pyrite. The two identified active acids in the deep groundwater are likely to control the base-flow chemistry of streams draining larger catchments (>1 km 2 ) as evident by δ 18 O signatures and base cation concentrations that overlap with that of the groundwater.

Carbon mineralization and pyrite oxidation in groundwater: Importance for silicate weathering in boreal forest soils and stream base-flow chemistry

Energy Technology Data Exchange (ETDEWEB)

Klaminder, J., E-mail: jonatan.klaminder@emg.umu.se [Department of Forest Ecology and Management, SLU, SE-901 83 Umea (Sweden)] [Department of Ecology and Environmental Science, Umea University, SE-901 87 (Sweden); Grip, H. [Department of Forest Ecology and Management, SLU, SE-901 83 Umea (Sweden); Moerth, C.-M. [Department of Geological Sciences, Stockholm University, 106 91 Stockholm (Sweden); Laudon, H. [Department of Forest Ecology and Management, SLU, SE-901 83 Umea (Sweden)

2011-03-15

Research highlights: {yields} Organic compounds is mineralized during later transport in deep groundwater aquifers. {yields} Carbonic acid generated by this process stimulates dissolution of silicate minerals. {yields} Protons derived from pyrite oxidation also affects weathering in deep groundwater. {yields} The identified weathering mechanisms affect base-flow chemistry in boreal streams. - Abstract: What role does mineralized organic C and sulfide oxidation play in weathering of silicate minerals in deep groundwater aquifers? In this study, how H{sub 2}CO{sub 3}, produced as a result of mineralization of organic matter during groundwater transport, affects silicate weathering in the saturated zone of the mineral soil along a 70 m-long boreal hillslope is demonstrated. Stream water measurements of base cations and {delta}{sup 18}O are included to determine the importance of the deep groundwater system for downstream surface water. The results suggest that H{sub 2}CO{sub 3} generated from organic compounds being mineralized during the lateral transport stimulates weathering at depths between 0.5 and 3 m in the soil. This finding is indicated by progressively increasing concentrations of base cations-, silica- and inorganic C (IC) in the groundwater along the hillslope that co-occur with decreasing organic C (OC) concentrations. Protons derived from sulfide oxidation appear to be an additional driver of the weathering process as indicated by a build-up of SO{sub 4}{sup 2-} in the groundwater during lateral transport and a {delta}{sup 34}S per mille value of +0.26-3.76 per mille in the deep groundwater indicating S inputs from pyrite. The two identified active acids in the deep groundwater are likely to control the base-flow chemistry of streams draining larger catchments (>1 km{sup 2}) as evident by {delta}{sup 18}O signatures and base cation concentrations that overlap with that of the groundwater.

Three Packets of Minerals of the Periodic Table of Chemical Elements and Chemical Compounds

OpenAIRE

Labushev, Mikhail M.

2013-01-01

The concepts of alpha- and beta-packets of the periodic table of chemical elements and chemical compounds are defined. The first of the 47 minerals alpha-packets is composed. In it all minerals are arranged in increasing Iav index of proportionality of atomic weights of composing chemical elements, the same way as chemical elements are located in increasing atomic weights in the Periodic table. The packet includes 93 known minerals and two compounds - N2O5 and CO2 - being actually minerals. B...

The effects of climate and landscape position on chemical denudation and mineral transformation in the Santa Catalina mountain critical zone observatory

International Nuclear Information System (INIS)

Lybrand, Rebecca; Rasmussen, Craig; Jardine, Angie; Troch, Peter; Chorover, Jon

2011-01-01

Highlights: → Depth to paralithic contact generally increased with elevation. → Q/P ratios were higher in divergent landscape positions compared to adjacent convergent hollows. → Clay mineral assemblages changed as a function of elevation. → Climate, landscape position and erosion interactively control soil and regolith development. - Abstract: Understanding the interactions of climate, physical erosion, chemical weathering and pedogenic processes is essential when considering the evolution of critical zone systems. Interactions among these components are particularly important to predicting how semiarid landscapes will respond to forecasted changes in precipitation and temperature under future climate change. The primary goal of this study was to understand how climate and landscape structure interact to control chemical denudation and mineral transformation across a range of semiarid ecosystems in southern Arizona. The research was conducted along the steep environmental gradient encompassed by the Santa Catalina Mountains Critical Zone Observatory (SCM-CZO). The gradient is dominated by granitic parent materials and spans significant range in both mean annual temperature (>10 deg. C) and precipitation (>50 cm a -1 ), with concomitant shift in vegetation communities from desert scrub to mixed conifer forest. Regolith profiles were sampled from divergent and convergent landscape positions in five different ecosystems to quantify how climate-landscape position interactions control regolith development. Regolith development was quantified as depth to paralithic contact and degree of chemical weathering and mineral transformation using a combination of quantitative and semi-quantitative X-ray diffraction (XRD) analyses of bulk soils and specific particle size classes. Depth to paralithic contact was found to increase systematically with elevation for divergent positions at approximately 28 cm per 1000 m elevation, but varied inconsistently for convergent

The effects of climate and landscape position on chemical denudation and mineral transformation in the Santa Catalina mountain critical zone observatory

Energy Technology Data Exchange (ETDEWEB)

Lybrand, Rebecca, E-mail: rlybrand@email.arizona.edu [Department of Soil, Water and Environmental Science, University of Arizona, Tucson, AZ 85721 (United States); Rasmussen, Craig [Department of Soil, Water and Environmental Science, University of Arizona, Tucson, AZ 85721 (United States); Jardine, Angie; Troch, Peter [Department of Hydrology and Water Resources, University of Arizona, Tucson, AZ 85721 (United States); Chorover, Jon [Department of Soil, Water and Environmental Science, University of Arizona, Tucson, AZ 85721 (United States)

2011-06-15

Highlights: > Depth to paralithic contact generally increased with elevation. > Q/P ratios were higher in divergent landscape positions compared to adjacent convergent hollows. > Clay mineral assemblages changed as a function of elevation. > Climate, landscape position and erosion interactively control soil and regolith development. - Abstract: Understanding the interactions of climate, physical erosion, chemical weathering and pedogenic processes is essential when considering the evolution of critical zone systems. Interactions among these components are particularly important to predicting how semiarid landscapes will respond to forecasted changes in precipitation and temperature under future climate change. The primary goal of this study was to understand how climate and landscape structure interact to control chemical denudation and mineral transformation across a range of semiarid ecosystems in southern Arizona. The research was conducted along the steep environmental gradient encompassed by the Santa Catalina Mountains Critical Zone Observatory (SCM-CZO). The gradient is dominated by granitic parent materials and spans significant range in both mean annual temperature (>10 deg. C) and precipitation (>50 cm a{sup -1}), with concomitant shift in vegetation communities from desert scrub to mixed conifer forest. Regolith profiles were sampled from divergent and convergent landscape positions in five different ecosystems to quantify how climate-landscape position interactions control regolith development. Regolith development was quantified as depth to paralithic contact and degree of chemical weathering and mineral transformation using a combination of quantitative and semi-quantitative X-ray diffraction (XRD) analyses of bulk soils and specific particle size classes. Depth to paralithic contact was found to increase systematically with elevation for divergent positions at approximately 28 cm per 1000 m elevation, but varied inconsistently for convergent

Physical-chemical study of hydroxi-phosphates and associated minerals occurring in the Pirocaua Plateau (MA) and Jandia hill (PA)

International Nuclear Information System (INIS)

Reymao, M. de F.F.

1983-01-01

A lateritic profile rich in alumino-calcic and aluminum hidroxi-phosphates (Pirocaua, MA), and another also rich in alumino-calcic and containning iron and calcium hidroxi-phosphates (Jandia, PA) has been investigated in order to elucidate the formation of the secondary minerals and the trace element behaviour during tropical weathering. For such purposes it was decided to use X-ray diffractometry and chemical analysis and it was pointed out the applicability of infrared absorption spectroscopy and differential thermal analysis for the mineral characterization. In order to relate the geochemical alterations it was included a theoretical thermodynamic study. Infrared absorption spectroscopy and differential thermal analysis have been demonstrated to be valuables methods for studying minerals. Results are presented which demonstrate the usefullness of these techniques. These studies show that it is now possible to correlate differential thermal analysis and infrared data with that from other techniques (chemical analysis, X-ray diffraction patterns) and that the methods yields valuable supplemental information. Theoretical calculations and the use of thermodynamic data (standard free energie and solubility products) reveal some important conclusions about chemical equilibria, mineral formation, solubility and stability relations. (Author) [pt

Mineral composition and geochemistry of the Upper Cretaceous siliciclastics (Nubia Group), Aswan District, south Egypt: Implications for provenance and weathering

Science.gov (United States)

Hassan, Abdallah M.

2017-11-01

The Upper-Cretaceous clastic succession (Nubia Group) in the area northeast of Aswan includes three rock units, from base upwards: Abu Aggag Formation (Turonian), Timsah Formation (Coniacian -Santonian) and Um Barmil Formation (Santonian - Campanian). Quartz and clay minerals are the predominant phases throughout the whole succession while feldspars are very rare. Kaolinite is overwhelming among the clay minerals, in addition to less important amounts of illite and illite/smectite. The ultrastable heavy minerals are the prevailing non- opaque phases and they significantly change in relative abundance upsection. SiO2, Al2O3 and Fe2O3 are the dominant chemical components. The statistical examination had revealed that the chemical constituents are loaded on three main geochemical trends; the siliceous, the argillaceous and the ferruginous. The enrichment factor shows that the geochemical behavior of the major and trace elements is uniform throughout the sandstones and mudstones of the Abu Aggag Formation. A significant geochemical contrast is documented between the sandstones and mudstones of both the Timsah and the Um Barmil formations. The provenance - critical elemental ratios Ti/Nb and Ti/Y are nearly constant throughout the sandstones and mudstones of the Abu Aggag Formation, and they fall within the range of granitic-granodioritic composition. The Timsah sandstones have Ti/Nb and Ti/Y ratios that are consistent with those of the Abu Aggag rocks, suggesting a similar provenance. These elemental ratios are extremely higher in the Timsah mudstones, reflecting a great influx of mafic material. The Um Barmil sandstones exhibit exceedingly dispersed values of Ti/Nb and Ti/Y, reflecting their derivation from large catchment's areas of different rock types with the eroded products being mixed in various relative proportions. The Ti/Nb and Ti/Y of the Um Barmil mudstones are closely akin to those of the Timsah mudstones suggesting analogous source. The chemical index of

Relationships between CO2, thermodynamic limits on silicate weathering, and the strength of the silicate weathering feedback

Science.gov (United States)

Winnick, Matthew J.; Maher, Kate

2018-03-01

Recent studies have suggested that thermodynamic limitations on chemical weathering rates exert a first-order control on riverine solute fluxes and by extension, global chemical weathering rates. As such, these limitations may play a prominent role in the regulation of carbon dioxide levels (pCO2) over geologic timescales by constraining the maximum global weathering flux. In this study, we develop a theoretical scaling relationship between equilibrium solute concentrations and pCO2 based on equilibrium constants and reaction stoichiometry relating primary mineral dissolution and secondary mineral precipitation. We test this theoretical scaling relationship against reactive transport simulations of chemical weathering profiles under open- and closed-system conditions, representing partially and fully water-saturated regolith, respectively. Under open-system conditions, equilibrium bicarbonate concentrations vary as a power-law function of pCO2 (y = kxn) where n is dependent on reaction stoichiometry and k is dependent on both reaction stoichiometry and the equilibrium constant. Under closed-system conditions, bicarbonate concentrations vary linearly with pCO2 at low values and approach open-system scaling at high pCO2. To describe the potential role of thermodynamic limitations in the global silicate weathering feedback, we develop a new mathematical framework to assess weathering feedback strength in terms of both (1) steady-state atmospheric pCO2 concentrations, and (2) susceptibility to secular changes in degassing rates and transient carbon cycle perturbations, which we term 1st and 2nd order feedback strength, respectively. Finally, we discuss the implications of these results for the effects of vascular land plant evolution on feedback strength, the potential role of vegetation in controlling modern solute fluxes, and the application of these frameworks to a more complete functional description of the silicate weathering feedback. Most notably, the dependence

Chemical weathering outputs from the flood plain of the Ganga

Science.gov (United States)

Bickle, Michael J.; Chapman, Hazel J.; Tipper, Edward; Galy, Albert; De La Rocha, Christina L.; Ahmad, Talat

2018-03-01

Transport of sediment across riverine flood plains contributes a significant but poorly constrained fraction of the total chemical weathering fluxes from rapidly eroding mountain belts which has important implications for chemical fluxes to the oceans and the impact of orogens on long term climate. We report water and bedload chemical analyses from the Ganges flood-plain, a major transit reservoir of sediment from the Himalayan orogen. Our data comprise six major southern tributaries to the Ganga, 31 additional analyses of major rivers from the Himalayan front in Nepal, 79 samples of the Ganga collected close to the mouth below the Farakka barrage every two weeks over three years and 67 water and 8 bedload samples from tributaries confined to the Ganga flood plain. The flood plain tributaries are characterised by a shallow δ18O - δD array, compared to the meteoric water line, with a low δDexcess from evaporative loss from the flood plain which is mirrored in the higher δDexcess of the mountain rivers in Nepal. The stable-isotope data confirms that the waters in the flood plain tributaries are dominantly derived from flood plain rainfall and not by redistribution of waters from the mountains. The flood plain tributaries are chemically distinct from the major Himalayan rivers. They can be divided into two groups. Tributaries from a small area around the Kosi river have 87Sr/86Sr ratios >0.75 and molar Na/Ca ratios as high as 6. Tributaries from the rest of the flood plain have 87Sr/86Sr ratios ≤0.74 and most have Na/Ca ratios waters have lost up to 70% of their Ca (average ∼ 50%) to precipitation of secondary calcite which is abundant as a diagenetic cement in the flood plain sediments. 31% of the Sr, 8% of the Ca and 45% of the Mg are calculated to be derived from silicate minerals. Because of significant evaporative loss of water across the flood plain, and in the absence of hydrological data for flood plain tributaries, chemical weathering fluxes from the

Chemical and colloidal aspects of collectorless flotation behavior of sulfide and non-sulfide minerals.

Science.gov (United States)

Aghazadeh, Sajjad; Mousavinezhad, Seyed Kamal; Gharabaghi, Mahdi

2015-11-01

Flotation has been widely used for separation of valuable minerals from gangues based on their surface characterizations and differences in hydrophobicity on mineral surfaces. As hydrophobicity of minerals widely differs from each other, their separation by flotation will become easier. Collectors are chemical materials which are supposed to make selectively valuable minerals hydrophobic. In addition, there are some minerals which based on their surface and structural features are intrinsically hydrophobic. However, their hydrophobicities are not strong enough to be floatable in the flotation cell without collectors such as sulfide minerals, coal, stibnite, and so forth. To float these minerals in a flotation cell, their hydrophobicity should be increased in specific conditions. Various parameters including pH, Eh, size distribution, mill types, mineral types, ore characterization, and type of reaction in flotation cells affect the hydrophobicity of minerals. Surface analysis results show that when sulfide minerals experience specific flotation conditions, the reactions on the surface of these minerals increase the amount of sulfur on the surface. These phenomenons improve the hydrophobicity of these minerals due to strong hydrophobic feature of sulfurs. Collectorless flotation reduces chemical material consumption amount, increases flotation selectivity (grade increases), and affects the equipment quantities; however, it can also have negative effects. Some minerals with poor surface floatability can be increased by adding some ions to the flotation system. Depressing undesirable minerals in flotation is another application of collectorless flotation.

Chemical weathering in response to tectonic uplift and denudation rate in a semi-arid environment, southeast Spain

Science.gov (United States)

Ameijeiras-Mariño, Yolanda; Opfergelt, Sophie; Schoonejans, Jérôme; Vanacker, Veerle; Sonnet, Philippe; Delmelle, Pierre

2014-05-01

Soil thickness reflects the balance between soil production and denudation by chemical weathering and physical erosion. At topographic steady state, the soil weathering intensity is expected to be higher at low denudation rate (transport-limited) than at high denudation rate (weathering-limited). We tested this hypothesis for the first time in a semi-arid environment where chemical weathering processes are generally slow. The study site is the Internal Zone of the Betic Cordillera in Southeast Spain, Almeria province. The lithology is mainly mica-schist and quartzite with local presence of phyllite. Three catchments (EST, FIL, CAB) were selected upstream local faults along a gradient of increasing uplift rates (10-170 mm/kyr) and increasing denudation rates (20-250 mm/kyr), following the sequence ESTweathering intensity. Three independent indices were used to compare soil weathering intensity across the EST, FIL and CAB catchments: the Total Reserve in Bases (TRB = [Ca2+] + [Na+] + [K+] + [Mg2+]); the soil Fed/Fet ratio that reflects the formation of secondary Fe-oxides, and the Cation Exchange Capacity (CEC) that varies with the amount of secondary clay minerals and organic matter. The difference in TRB between the soil and the bedrock (ΔTRB = TRB soil - TRB bedrock) should be more negative as weathering increases, whereas the Fed/Fet ratio is expected to augment with the intensity of weathering. Since these soils have low organic carbon content, the CEC should increase with weathering degree. Our results indicate that the ΔTRB (cmolc.kg-1) is -8±14 (n=8), -79±2 (n=8) and -51±38 (n=9) for CAB, FIL and EST, respectively. The Fed/Fet ratio for CAB, FIL and EST is 0.20±0.05 (n=8), 0.20±0.03 (n=8) and 0.29±0.05 (n=9), respectively. The CEC (cmolc.kg-1) increases from 3.3�

A subsurface Fe-silicate weathering microbiome

Science.gov (United States)

Napieralski, S. A.; Buss, H. L.; Roden, E. E.

2017-12-01

from enrichment cultures provides insight into the role of FeOB in Fe(II)-mineral alteration as well as furthering our understanding of the biotic reactions contributing the globally important biogeochemical phenomenon of chemical weathering.

Constraints on continental crustal mass loss via chemical weathering using lithium and its isotopes

Science.gov (United States)

Rudnick, R. L.; Liu, X. M.

2012-04-01

The continental crust has an "intermediate" bulk composition that is distinct from primary melts of peridotitic mantle (basalt or picrite). This mismatch between the "building blocks" and the "edifice" that is the continental crust points to the operation of processes that preferentially remove mafic to ultramafic material from the continents. Such processes include lower crustal recycling (via density foundering or lower crustal subduction - e.g., relamination, Hacker et al., 2011, EPSL), generation of evolved melts via slab melting, and/or chemical weathering. Stable isotope systems point to the influence of chemical weathering on the bulk crust composition: the oxygen isotope composition of the bulk crust is distinctly heavier than that of primary, mantle-derived melts (Simon and Lecuyer, 2005, G-cubed) and the Li isotopic composition of the bulk crust is distinctly lighter than that of mantle-derive melts (Teng et al., 2004, GCA; 2008, Chem. Geol.). Both signatures mark the imprint of chemical weathering on the bulk crust composition. Here, we use a simple mass balance model for lithium inputs and outputs from the continental crust to quantify the mass lost due to chemical weathering. We find that a minimum of 15%, a maximum of 60%, and a best estimate of ~40% of the original juvenile rock mass may have been lost via chemical weathering. The accumulated percentage of mass loss due to chemical weathering leads to an average global chemical weathering rate (CWR) of ~ 1×10^10 to 2×10^10 t/yr since 3.5 Ga, which is about an order of magnitude higher than the minimum estimates based on modern rivers (Gaillardet et al., 1999, Chem. Geol.). While we cannot constrain the exact portion of crustal mass loss via chemical weathering, given the uncertainties of the calculation, we can demonstrate that the weathering flux is non-zero. Therefore, chemical weathering must play a role in the evolution of the composition and mass of the continental crust.

The importance of non-carbonate mineral weathering as a soil formation mechanism within a karst weathering profile in the SPECTRA Critical Zone Observatory, Guizhou Province, China

Institute of Scientific and Technical Information of China (English)

Oliver W.Moore; Heather L.Buss; Sophie M.Green; Man Liu; Zhaoliang Song

2017-01-01

Soil degradation,including rocky desertification,of the karst regions in China is severe.Karst landscapes are especially sensitive to soil degradation as carbonate rocks are nutrient-poor and easily eroded.Understanding the balance between soil formation and soil erosion is critical for long-term soil sustainability,yet little is known about the initial soil forming processes on karst terrain.Herein we examine the initial weathering processes of several types of carbonate bedrock containing varying amounts of non-carbonate minerals in the SPECTRA Critical Zone Observatory,Guizhou Province,Southwest China.We compared the weathering mechanisms of the bedrock to the mass transfer of mineral nutrients in a soil profile developed on these rocks and found that soil formation and nutrient contents are strongly dependent upon the weathering of interbedded layers of more silicate-rich bedrock (marls).Atmospheric inputs from dust were also detected.

Chemical weathering from the CoDA (Compositional Data Analysis) point of view: new insights for the Alpine rivers geochemistry

Science.gov (United States)

Gozzi, Caterina; Buccianti, Antonella; Frondini, Francesco

2017-04-01

The aim of this contribution is to explore the relationship among weathering reactions, the sample space of compositional data and fractals by means of distributional analysis. Weathering reactions represent the transfer of heat and entropy to the environment in geochemical cycles. Chemical weathering is a key process for understanding the global cycle of elements, both on long and short-terms and chemical weathering rates are complex functions of many factors including dissolution kinetics of minerals, mechanical erosion, lithology. Compositional data express the relative (proportional) abundance of chemical elements/species in a given total (i.e. volume or weight) so that compositions pertaining to the peculiar geometry of the simplex sample space. Fractals are temporal or spatial objects with self-similarity and scale invariance, so that internal structures repeat themselves over multiple levels of magnification or scales of measurement. Gibbs's free energy and the application of the Law Mass Action can be used to model weathering reactions, under the hypothesis of chemical equilibrium. Compositional data are obtained in the analytical phase after the determination of the concentrations of chemicals in sampled solid, liquid or gaseous materials. Fractals can be measured by using their fractal dimensions. The presence of fractal structures can be observed when the frequency distribution of isometric log-ratio coordinates is investigated, showing the logarithm of the cumulative number of samples exceeding a certain coordinate value plotted against the coordinate value itself. Isometric log-ratio coordinates (or balances) can be constructed by using the sequential binary partition (SBP) method. The balances can be identified to maintain, as far as possible, the similarity with a corresponding weathering reaction (Buccianti & Zuo, 2016). As an alternative, balances can be derived after the multivariate investigation of the variance-covariance structure of the

Chemical weathering of a marine terrace chronosequence, Santa Cruz, California I: Interpreting rates and controls based on soil concentration-depth profiles

Science.gov (United States)

White, A.F.; Schulz, M.S.; Vivit, D.V.; Blum, A.E.; Stonestrom, David A.; Anderson, S.P.

2008-01-01

The spatial and temporal changes in element and mineral concentrations in regolith profiles in a chronosequence developed on marine terraces along coastal California are interpreted in terms of chemical weathering rates and processes. In regoliths up to 15 m deep and 226 kyrs old, quartz-normalized mass transfer coefficients indicate non-stoichiometric preferential release of Sr > Ca > Na from plagioclase along with lesser amounts of K, Rb and Ba derived from K-feldspar. Smectite weathering results in the loss of Mg and concurrent incorporation of Al and Fe into secondary kaolinite and Fe-oxides in shallow argillic horizons. Elemental losses from weathering of the Santa Cruz terraces fall within the range of those for other marine terraces along the Pacific Coast of North America. Residual amounts of plagioclase and K-feldspar decrease with terrace depth and increasing age. The gradient of the weathering profile bs is defined by the ratio of the weathering rate, R to the velocity at which the profile penetrates into the protolith. A spreadsheet calculator further refines profile geometries, demonstrating that the non-linear regions at low residual feldspar concentrations at shallow depth are dominated by exponential changes in mineral surface-to-volume ratios and at high residual feldspar concentrations, at greater depth, by the approach to thermodynamic saturation. These parameters are of secondary importance to the fluid flux qh, which in thermodynamically saturated pore water, controls the weathering velocity and mineral losses from the profiles. Long-term fluid fluxes required to reproduce the feldspar weathering profiles are in agreement with contemporary values based on solute Cl balances (qh = 0.025-0.17 m yr-1). During saturation-controlled and solute-limited weathering, the greater loss of plagioclase relative to K-feldspar is dependent on the large difference in their respective solubilities instead of the small difference between their respective

Quantifying chemical weathering rates along a precipitation gradient on Basse-Terre Island, French Guadeloupe: new insight from U-series isotopes in weathering rinds

Science.gov (United States)

Engel, Jacqueline M.; May, Linda; Sak, Peter B.; Gaillardet, Jerome; Ren, Minghua; Engle, Mark A.; Brantley, Susan L.

2016-01-01

Inside soil and saprolite, rock fragments can form weathering clasts (alteration rinds surrounding an unweathered core) and these weathering rinds provide an excellent field system for investigating the initiation of weathering and long term weathering rates. Recently, uranium-series (U-series) disequilibria have shown great potential for determining rind formation rates and quantifying factors controlling weathering advance rates in weathering rinds. To further investigate whether the U-series isotope technique can document differences in long term weathering rates as a function of precipitation, we conducted a new weathering rind study on tropical volcanic Basse-Terre Island in the Lesser Antilles Archipelago. In this study, for the first time we characterized weathering reactions and quantified weathering advance rates in multiple weathering rinds across a steep precipitation gradient. Electron microprobe (EMP) point measurements, bulk major element contents, and U-series isotope compositions were determined in two weathering clasts from the Deshaies watershed with mean annual precipitation (MAP) = 1800 mm and temperature (MAT) = 23 °C. On these clasts, five core-rind transects were measured for locations with different curvature (high, medium, and low) of the rind-core boundary. Results reveal that during rind formation the fraction of elemental loss decreases in the order: Ca ≈ Na > K ≈ Mg > Si ≈ Al > Zr ≈ Ti ≈ Fe. Such observations are consistent with the sequence of reactions after the initiation of weathering: specifically, glass matrix and primary minerals (plagioclase, pyroxene) weather to produce Fe oxyhydroxides, gibbsite and minor kaolinite.Uranium shows addition profiles in the rind due to the infiltration of U-containing soil pore water into the rind as dissolved U phases. U is then incorporated into the rind as Fe-Al oxides precipitate. Such processes lead to significant U-series isotope disequilibria in the rinds

Biogeochemical weathering of serpentinites: An examination of incipient dissolution affecting serpentine soil formation

International Nuclear Information System (INIS)

Baumeister, Julie L.; Hausrath, Elisabeth M.; Olsen, Amanda A.; Tschauner, Oliver; Adcock, Christopher T.; Metcalf, Rodney V.

2015-01-01

Highlights: • Dissolution of primary minerals is important to porosity generation in serpentinites. • Mineral weathering extent in serpentinites follows the order Fe > Mg > Al rich minerals. • Fe-oxidizing bacteria may mediate Fe-rich primary and serpentine mineral alteration. • Serpentinite weathering is strongly impacted by degree of serpentinization. - Abstract: Serpentinite rocks, high in Mg and trace elements including Ni, Cr, Cd, Co, Cu, and Mn and low in nutrients such as Ca, K, and P, form serpentine soils with similar chemical properties resulting in chemically extreme environments for the biota that grow upon them. The impact of parent material on soil characteristics is most important in young soils, and therefore the incipient weathering of serpentinite rock likely has a strong effect on the development of serpentine soils and ecosystems. Additionally, porosity generation is a crucial process in converting rock into a soil that can support vegetation. Here, the important factors affecting the incipient weathering of serpentinite rock are examined at two sites in the Klamath Mountains, California. Serpentinite-derived soils and serpentinite rock cores were collected in depth profiles from each sampling location. Mineral dissolution in weathered serpentinite samples, determined by scanning electron microscopy, energy dispersive spectrometry, electron microprobe analyses, and synchrotron microXRD, is consistent with the order, from most weathered to least weathered: Fe-rich pyroxene > antigorite > Mg-rich lizardite > Al-rich lizardite. These results suggest that the initial porosity formation within serpentinite rock, impacting the formation of serpentine soil on which vegetation can exist, is strongly affected both by the presence of non-serpentine primary minerals as well as the composition of the serpentine minerals. In particular, the presence of ferrous Fe appears to contribute to greater dissolution, whereas the presence of Al within the

Weathering of the New Albany Shale, Kentucky, USA: I. Weathering zones defined by mineralogy and major-element composition

Science.gov (United States)

Tuttle, M.L.W.; Breit, G.N.

2009-01-01

Comprehensive understanding of chemical and mineralogical changes induced by weathering is valuable information when considering the supply of nutrients and toxic elements from rocks. Here minerals that release and fix major elements during progressive weathering of a bed of Devonian New Albany Shale in eastern Kentucky are documented. Samples were collected from unweathered core (parent shale) and across an outcrop excavated into a hillside 40 year prior to sampling. Quantitative X-ray diffraction mineralogical data record progressive shale alteration across the outcrop. Mineral compositional changes reflect subtle alteration processes such as incongruent dissolution and cation exchange. Altered primary minerals include K-feldspars, plagioclase, calcite, pyrite, and chlorite. Secondary minerals include jarosite, gypsum, goethite, amorphous Fe(III) oxides and Fe(II)-Al sulfate salt (efflorescence). The mineralogy in weathered shale defines four weathered intervals on the outcrop-Zones A-C and soil. Alteration of the weakly weathered shale (Zone A) is attributed to the 40-a exposure of the shale. In this zone, pyrite oxidization produces acid that dissolves calcite and attacks chlorite, forming gypsum, jarosite, and minor efflorescent salt. The pre-excavation, active weathering front (Zone B) is where complete pyrite oxidation and alteration of feldspar and organic matter result in increased permeability. Acidic weathering solutions seep through the permeable shale and evaporate on the surface forming abundant efflorescent salt, jarosite and minor goethite. Intensely weathered shale (Zone C) is depleted in feldspars, chlorite, gypsum, jarosite and efflorescent salts, but has retained much of its primary quartz, illite and illite-smectite. Goethite and amorphous FE(III) oxides increase due to hydrolysis of jarosite. Enhanced permeability in this zone is due to a 14% loss of the original mass in parent shale. Denudation rates suggest that characteristics of Zone C

Differential chemical fractionation of dissolved organic matter during sorption by Fe mineral phases in a tropical soil from the Luquillo Critical Zone Observatory

Science.gov (United States)

Plante, A. F.; Coward, E.; Ohno, T.; Thompson, A.

2017-12-01

Fe-bearing mineral phases contribute substantially to adsorption and stabilization of soil organic matter (SOM), due largely to their high specific surface area (SSA) and reactivity. While the importance of adsorption onto mineral surfaces has been well-elucidated, selectivity of various mineral and organic phases remains poorly understood. The goals of this work were to: 1) quantify the contributions of Fe-minerals of varying crystallinity to dissolved organic matter (DOM) sorption, and 2) characterize the molecular fractionation of DOM induced by reactions at the mineral interface, using a highly-weathered Oxisol from the Luquillo Critical Zone Observatory (LCZO). Three selective dissolution experiments targeting Fe-mineral phases were followed by specific surface area (SSA) analysis of the residues and characterization of extracted DOM by high resolution mass spectrometry (FT-ICR-MS). Fe-depleted extraction residue samples, untreated control soil samples, and Fe-enriched ferrihydrite-coated soil samples were then subjected to a batch sorption experiment with litter-derived DOM. Results of selective dissolution experiments indicated that a substantial proportion of soil SSA was derived from extracted Fe-bearing phases, and FT-ICR-MS analysis of extracted DOM revealed distinct chemical signatures. Sorbed C concentrations were well correlated with Fe contents induced by treatments, and thus SSA. Molecular characterization of the DOM post-sorption indicated that poorly crystalline Fe phases preferentially adsorbed highly unsaturated aromatic compounds, and higher-crystallinity Fe phases were associated with more aliphatic compounds. These findings suggests that molecular fractionation via organomineral complexation may act as a physicochemical filter of DOM released to the critical zone.

Chemical weathering on Mars. Collection of papers. LPI-MSATT Workshop on Chemical Weathering on Mars, Cocoa Beach, FL (USA), 10 - 12 Sep 1992.

Science.gov (United States)

Burns, R. G.; Banin, A.

1993-10-01

The Workshop on Chemical Weathering on Mars consisted of thirty papers, extended abstracts of which were published in the LPI Technical Report, No. 92-04. The collection of seven papers in this issue report new data and interpretations about the chemical evolution of the Martian surface.

The effects of weathering on the physical and mechanical properties of igneous and metamorphic saprolites

DEFF Research Database (Denmark)

Rocchi, Irene; Coop, M. R.; Maccarini, M.

2017-01-01

The present paper presents three extensive datasets of laboratory testing on weathered geomaterials, which are emblematic of soil types widely found worldwide. The overall dataset includes soils originating from igneous and metamorphic rocks, either coarse or fine grained and having either felsic...... or mafic minerals. In particular, the data are interpreted to highlight the effects that weathering has on the physical and mechanical properties of these natural geomaterials comparing them with published data with the aim to provide a general framework of interpretation that takes into account...... this geological process and links soil mechanics to engineering geology. Generally, weathering induces a reduction in the grain size, both due to physical actions (e.g. opening of grain contacts) and to the chemical decomposition of minerals resulting in the formation of clay minerals. As weathering proceeds...

Assessment of the geoavailability of trace elements from minerals in mine wastes: analytical techniques and assessment of selected copper minerals

Science.gov (United States)

Driscoll, Rhonda; Hageman, Phillip L.; Benzel, William M.; Diehl, Sharon F.; Adams, David T.; Morman, Suzette; Choate, LaDonna M.

2012-01-01

In this study, four randomly selected copper-bearing minerals were examined—azurite, malachite, bornite, and chalcopyrite. The objectives were to examine and enumerate the crystalline and chemical properties of each of the minerals, to determine which, if any, of the Cu-bearing minerals might adversely affect systems biota, and to provide a multi-procedure reference. Laboratory work included use of computational software for quantifying crystalline and amorphous material and optical and electron imaging instruments to model and project crystalline structures. Chemical weathering, human fluid, and enzyme simulation studies were also conducted. The analyses were conducted systematically: X-ray diffraction and microanalytical studies followed by a series of chemical, bio-leaching, and toxicity experiments.

Space-weathering processes and products on volatile-rich asteroids

Science.gov (United States)

Britt, D.; Schelling, P.; Consolmagno, G.; Bradley, T.

2014-07-01

Space weathering is a generic term for the effects on atmosphereless solid bodies in the solar system from a range of processes associated with direct exposure to the space environment. These include impact processes (shock, vaporization, fragmentation, heating, melting, and ejecta formation), radiation damage (from galactic and solar cosmic rays), solar-wind effects (irradiation, ion implantation, and sputtering), and the chemical reactions driven by these processes. The classic example of space weathering is the formation of the lunar spectral red slope associated with the production of nanophase Fe (npFe0) in the dusty lunar regolith (C.R. Chapman, 2004, Annual Review of Earth & Planet. Sci. 32, C.M. Pieters, 2000, MAPS 35). Similar npFe0 has been recovered from asteroid (25143) Itokawa and some asteroid classes do exhibit modest spectral red slopes (T. Noguchi, 2011, Science 333). Space weathering can be thought of as driven by a combination of the chemical environment of space (hard vacuum, low oxygen fugacity, solar-wind implantation of hydrogen) along with thermal energy supplied by micrometeorite impacts. The forward modeling of space weathering as thermodynamically-driven decomposition of common rock-forming minerals suggests the production of a range of daughter products: (1) The silicate products typically lose oxygen, other volatile elements (i.e., sulfur and sodium), and metallic cations, producing minerals that are typically more disordered and less optically active than the original parent materials. (2) The decomposed metallic cations form in nano-sized blebs including npFe0, on the surfaces or in condensing rims of mineral grains. This creates a powerful optical component as seen in the lunar red slope. Surfaces with exposed npFe0 are an ideal environment for catalyzing further reactions. (3) The liberated volatile elements and gases (O, S, Na) may form an observable exosphere (e.g., Moon and Mercury) and can either escape from the body or

Does Silicate Weathering of Loess Affect Atmospheric CO2?

Science.gov (United States)

Anderson, S. P.

2002-12-01

Weathering of glacial loess may be a significant, yet unrecognized, component of the carbon cycle. Glaciers produce fine-grained sediment, exposing vast amounts of mineral surface area to weathering processes, yet silicate mineral weathering rates at glacier beds and of glacial till are not high. Thus, despite the tremendous potential for glaciers to influence global weathering rates and atmospheric CO2 levels, this effect has not been demonstrated. Loess, comprised of silt-clay sizes, may be the key glacial deposit in which silicate weathering rates are high. Loess is transported by wind off braid plains of rivers, and deposited broadly (order 100 km from the source) in vegetated areas. Both the fine grain size, and hence large mineral surface area, and presence of vegetation should render loess deposits highly susceptible to silicate weathering. These deposits effectively extend the geochemical impact of glaciation in time and space, and bring rock flour into conditions conducive to chemical weathering. A simple 1-d model of silicate weathering fluxes from a soil profile demonstrates the potential of loess deposition to enhance CO2 consumption. At each time step, computed mineral dissolution (using anorthite and field-based rate constants) modifies the size of mineral grains within the soil. In the case of a stable soil surface, this results in a gradual decline in weathering fluxes and CO2 consumption through time, as finer grain sizes dissolve away. Computed weathering fluxes for a typical loess, with an initial mean grain size of 25 μm, are an order of magnitude greater than fluxes from a non-loess soil that differs only in having a mean grain size of 320 μm. High weathering fluxes are maintained through time if loess is continually deposited. Deposition rates as low as 0.01 mm/yr (one loess grain thickness per year) can lead to a doubling of CO2 consumption rates within 5 ka. These results suggest that even modest loess deposition rates can significantly

Changes in the chemical composition of the light crude by short-term weathering

International Nuclear Information System (INIS)

Luo, X.; Ma, Q.M.

2006-01-01

In the event of an oil spill, it is important to unambiguously identify the oil and link it to the known source in order to determine environmental impact and legal liability. The fate and behaviour of spilled oil depends on several physical, chemical and biological factors such as evaporation, dissolution, microbial degradation and photooxidation. The chemical composition of the spilled oil changes with weathering. The changes can have a significant effect on the oil's toxicity and can add to the difficulty of identifying spilled oil. This paper presents the results of changes in chemical composition of light crude oil by weathering under natural environmental conditions. Oil samples were analyzed on a gas chromatograph equipped with a mass selective detector. Light crude oil was obtained from the oil cabin of a tanker which spilled oil near the Dalian Sea near China in April 2005. It was shown that the saturated hydrocarbons of light crude oil distribute between n-C 8 and n-C 23 . The most abundant n-alkanes are found in the n-C 10 to n-C 16 . The main chemical compositions of the light crude oil are the n-alkanes and the isoprenoids. The aromatic compounds are subordinate chemical compositions of the light crude oil. A simulated weathering experiment showed that less than n-C 12 of the n-alkanes, toluene, 1,3-dimethyl benzene is lost after 1 day of weathering. The n-C 13 , n-C 14 , naphthalene and 2-methyl-naphthalene are lost on the fifth day of weathering. N-C 15 alkane composition indicates some weatherproof capability. The ratios of n-C 17 /pristine and n-C 18 /phytane were unchanged and useful in identifying the source of the light crude oil during the first 8-day weathering period. By the twenty-first day of weathering, the chemical composition underwent extreme alteration, and the source of the pollution could not be determined by the ratios of pristine/phytane. 12 refs., 3 tabs., 7 figs

Identification of provenance rocks based on EPMA analyses of heavy minerals

Science.gov (United States)

Shimizu, M.; Sano, N.; Ueki, T.; Yonaga, Y.; Yasue, K. I.; Masakazu, N.

2017-12-01

Information on mountain building is significant in the field of geological disposal of high-level radioactive waste, because this affects long-term stability in groundwater flow system. Provenance analysis is one of effective approaches for understanding building process of mountains. Chemical compositions of heavy minerals, as well as their chronological data, can be an index for identification of provenance rocks. The accurate identification requires the measurement of as many grains as possible. In order to achieve an efficient provenance analysis, we developed a method for quick identification of heavy minerals using an Electron Probe Micro Analyzer (EPMA). In this method, heavy mineral grains extracted from a sample were aligned on a glass slide and mounted in a resin. Concentration of 28 elements was measured for 300-500 grains per sample using EPMA. To measure as many grains as possible, we prioritized swiftness of measurement over precision, configuring measurement time of about 3.5 minutes for each grain. Identification of heavy minerals was based on their chemical composition. We developed a Microsoft® Excel® spread sheet input criteria of mineral identification using a typical range of chemical compositions for each mineral. The grains of 110 wt.% total were rejected. The criteria of mineral identification were revised through the comparison between mineral identification by optical microscopy and chemical compositions of grains classified as "unknown minerals". Provenance rocks can be identified based on abundance ratio of identified minerals. If no significant difference of the abundance ratio was found among source rocks, chemical composition of specific minerals was used as another index. This method was applied to the sediments of some regions in Japan where provenance rocks had lithological variations but similar formation ages. Consequently, the provenance rocks were identified based on chemical compositions of heavy minerals resistant to

Radiogenic Isotopes in Weathering and Hydrology

Science.gov (United States)

Blum, J. D.; Erel, Y.

2003-12-01

There are a small group of elements that display variations in their isotopic composition, resulting from radioactive decay within minerals over geological timescales. These isotopic variations provide natural fingerprints of rock-water interactions and have been widely utilized in studies of weathering and hydrology. The isotopic systems that have been applied in such studies are dictated by the limited number of radioactive parent-daughter nuclide pairs with half-lives and isotopic abundances that result in measurable differences in daughter isotope ratios among common rocks and minerals. Prior to their application to studies of weathering and hydrology, each of these isotopic systems was utilized in geochronology and petrology. As in the case of their original introduction into geochronology and petrology, isotopic systems with the highest concentrations of daughter isotopes in common rocks and minerals and systems with the largest observed isotopic variations were introduced first and have made the largest impact on our understanding of weathering and hydrologic processes. Although radiogenic isotopes have helped elucidate many important aspects of weathering and hydrology, it is important to note that in almost every case that will be discussed in this chapter, our fundamental understanding of these topics came from studies of variations in the concentrations of major cations and anions. This chapter is a "tools chapter" and thus it will highlight applications of radiogenic isotopes that have added additional insight into a wide spectrum of research areas that are summarized in almost all of the other chapters of this volume.The first applications of radiogenic isotopes to weathering processes were based on studies that sought to understand the effects of chemical weathering on the geochronology of whole-rock samples and geochronologically important minerals (Goldich and Gast, 1966; Dasch, 1969; Blaxland, 1974; Clauer, 1979, 1981; Clauer et al., 1982); as well

Experimental Simulation of Long Term Weathering in Alkaline Bauxite Residue Tailings

Directory of Open Access Journals (Sweden)

Talitha C. Santini

2015-07-01

Full Text Available Bauxite residue is an alkaline, saline tailings material generated as a byproduct of the Bayer process used for alumina refining. Developing effective plans for the long term management of potential environmental impacts associated with storage of these tailings is dependent on understanding how the chemical and mineralogical properties of the tailings will change during weathering and transformation into a soil-like material. Hydrothermal treatment of bauxite residue was used to compress geological weathering timescales and examine potential mineral transformations during weathering. Gibbsite was rapidly converted to boehmite; this transformation was examined with in situ synchrotron XRD. Goethite, hematite, and calcite all precipitated over longer weathering timeframes, while tricalcium aluminate dissolved. pH, total alkalinity, and salinity (electrical conductivity all decreased during weathering despite these experiments being performed under “closed” conditions (i.e., no leaching. This indicates the potential for auto-attenuation of the high alkalinity and salinity that presents challenges for long term environmental management, and suggests that management requirements will decrease during weathering as a result of these mineral transformations.

Does runoff or temperature control chemical weathering rates?

International Nuclear Information System (INIS)

Eiriksdottir, Eydis Salome; Gislason, Sigurdur Reynir; Oelkers, Eric H.

2011-01-01

Highlights: → The rate chemical weathering is affected by both temperature and runoff. Separating out these two factors is challenging because runoff tends to increase with increasing temperature. → In this study, natural river water samples collected on basaltic catchments over a five year period are used together with experimentally derived dissolution rate model for basaltic glass to pull apart the effects of runoff and temperature. → This study shows that the rate of chemical denudation is controlled by both temperature and runoff, but is dominated by runoff. - Abstract: The rate of chemical denudation is controlled by both temperature and runoff. The relative role of these two factors in the rivers of NE Iceland is determined through the rigorous analysis of their water chemistry over a 5-a period. River catchments are taken to be analogous to laboratory flow reactors; like the fluid in flow reactors, the loss of each dissolved element in river water is the sum of that of the original rainwater plus that added from kinetically controlled dissolution and precipitation reactions. Consideration of the laboratory determined dissolution rate behaviour of basalts and measured water chemistry indicates that the maximum effect of changing temperature on chemical denudation in the NE Icelandic rivers was 5-25% of the total change, whereas that of runoff was 75-95%. The bulk of the increased denudation rates with runoff appear to stem from an increase in reactive surface area for chemical weathering of catchment solids.

Platinum-Group Minerals in Chromitites of the Niquelândia Layered Intrusion (Central Goias, Brazil: Their Magmatic Origin and Low-Temperature Reworking during Serpentinization and Lateritic Weathering

Directory of Open Access Journals (Sweden)

Nelson Angeli

2012-10-01

Full Text Available A variety of platinum-group-minerals (PGM have been found to occur associated with the chromitite and dunite layers in the Niquelândia igneous complex. Two genetically distinct populations of PGM have been identified corresponding to phases crystallized at high temperatures (primary, and others formed or modified during post-magmatic serpentinization and lateritic weathering (secondary. Primary PGM have been found in moderately serpentinized chromitite and dunite, usually included in fresh chromite grains or partially oxidized interstitial sulfides. Due to topographically controlled lateritic weathering, the silicate rocks are totally transformed to a smectite-kaolinite-garnierite-amorphous silica assemblage, while the chromite is changed into a massive aggregate of a spinel phase having low-Mg and a low Fe3+/Fe2+ ratio, intimately associated with Ti-minerals, amorphous Fe-hydroxides, goethite, hematite and magnetite. The PGM in part survive alteration, and in part are corroded as a result of deep chemical weathering. Laurite is altered to Ru-oxides or re-crystallizes together with secondary Mg-ilmenite. Other PGM, especially the Pt-Fe alloys, re-precipitate within the altered chromite together with kaolinite and Fe-hydroxides. Textural evidence suggests that re-deposition of secondary PGM took place during chromite alteration, controlled by variation of the redox conditions on a microscopic scale.

Intensity and duration of chemical weathering: An example from soil clays of the southeastern Koolau Mountains, Oahu, Hawaii

Science.gov (United States)

Johnsson, Mark J.; Ellen, Stephen D.; McKittrick, Mary Anne

1993-01-01

Orographic precipitation on the southern flank of the southeastern Koolau Mountains produces a pronounced precipitation gradient. The corresponding gradient in the intensity of the chemical weathering environment provides an opportunity to address the effects of varying chemical weathering intensity on the composition of clay-size weathering products in soils developed on basalt. In addition, little-modified remnants of the constructional surface of the Koolau Volcano, isolated by stream dissection, remain as facets on the southern ends of the parallel ridges of the study area. By comparing clay mineralogy of soils developed on these older geomorphic surfaces with those developed on the younger sharp-crested ridges and steep side slopes, the effects of weathering duration on clay mineralogy can also be addressed.Soil clays in this part of the Koolau Mountains are mineralogically complex; principal phases include smectite, kaolinite, and halloysite, but pure end member phases are uncommon. Rather, most phases contain some amount of mixed layering. Smectite may contain small (Volcano are markedly more leached than those from younger landscapes in the same precipitation regime. Although smectite may be present, kaolinite is the dominant phase, and accumulations of Fe and Ti occur in the uppermost soil levels. Enrichment of Zr and Ti in these soils, as compared to concentrations in the original basaltic parent material, indicates that as much as 75% of the parent material has been lost. Thus weathering duration may affect soil clay composition in the same way as weathering intensity.Because smectite and halloysite are expandable clay minerals, their presence in soils may decrease slope stability and influence the nature of slope processes. Soil avalanches occur on steep slopes throughout the study area, whereas slow-moving landslides appear to be restricted to gentler slopes in drier parts of the study area where smectite is abundant. The clay mineralogy of soils thus

The role of soil weathering and hydrology in regulating chemical fluxes from catchments (Invited)

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Maher, K.; Chamberlain, C. P.

2010-12-01

Catchment-scale chemical fluxes have been linked to a number of different parameters that describe the conditions at the Earth’s surface, including runoff, temperature, rock type, vegetation, and the rate of tectonic uplift. However, many of the relationships relating chemical denudation to surface processes and conditions, while based on established theoretical principles, are largely empirical and derived solely from modern observations. Thus, an enhanced mechanistic basis for linking global solute fluxes to both surface processes and climate may improve our confidence in extrapolating modern solute fluxes to past and future conditions. One approach is to link observations from detailed soil-based studies with catchment-scale properties. For example, a number of recent studies of chemical weathering at the soil-profile scale have reinforced the importance of hydrologic processes in controlling chemical weathering rates. An analysis of data from granitic soils shows that weathering rates decrease with increasing fluid residence times and decreasing flow rates—over moderate fluid residence times, from 5 days to 10 years, transport-controlled weathering explains the orders of magnitude variation in weathering rates to a better extent than soil age. However, the importance of transport-controlled weathering is difficult to discern at the catchment scale because of the range of flow rates and fluid residence times captured by a single discharge or solute flux measurement. To assess the importance of transport-controlled weathering on catchment scale chemical fluxes, we present a model that links the chemical flux to the extent of reaction between the soil waters and the solids, or the fluid residence time. Different approaches for describing the distribution of fluid residence times within a catchment are then compared with the observed Si fluxes for a limited number of catchments. This model predicts high solute fluxes in regions with high run-off, relief, and

Comparison of mineral weathering and biomass nutrient uptake in two small forested watersheds underlain by quartzite bedrock, Catoctin Mountain, Maryland, USA

Science.gov (United States)

Rice, Karen; Price, Jason R.

2014-01-01

To quantify chemical weathering and biological uptake, mass-balance calculations were performed on two small forested watersheds located in the Blue Ridge Physiographic Province in north-central Maryland, USA. Both watersheds, Bear Branch (BB) and Fishing Creek Tributary (FCT), are underlain by relatively unreactive quartzite bedrock. Such unreactive bedrock and associated low chemical-weathering rates offer the opportunity to quantify biological processes operating within the watershed. Hydrologic and stream-water chemistry data were collected from the two watersheds for the 9-year period from June 1, 1990 to May 31, 1999. Of the two watersheds, FCT exhibited both higher chemical-weathering rates and biomass nutrient uptake rates, suggesting that forest biomass aggradation was limited by the rate of chemical weathering of the bedrock. Although the chemical-weathering rate in the FCT watershed was low relative to the global average, it masked the influence of biomass base-cation uptake on stream-water chemistry. Any differences in bedrock mineralogy between the two watersheds did not exert a significant influence on the overall weathering stoichiometry. The difference in chemical-weathering rates between the two watersheds is best explained by a larger proportion of reactive phyllitic layers within the bedrock of the FCT watershed. Although the stream gradient of BB is about two-times greater than that of FCT, its influence on chemical weathering appears to be negligible. The findings of this study support the biomass nutrient uptake stoichiometry of K1.0Mg1.1Ca0.97 previously determined for the study site. Investigations of the chemical weathering of relatively unreactive quartzite bedrock may provide insight into critical zone processes.

Environmental Impact Specification for Direct Space Weathering of Kuiper Belt and Oort Cloud Objects

Science.gov (United States)

Cooper, John F.

2010-01-01

The Direct Space Weathering Project of NASA's Outer Planets Research Program addresses specification of the plasma and energetic particle environments for irradiation and surface chemical processing of icy bodies in the outer solar system and the local interstellar medium. Knowledge of the radiation environments is being expanded by ongoing penetration of the twin Voyager spacecraft into the heliosheath boundary region of the outer heliosphere and expected emergence within the next decade into the very local interstellar medium. The Voyager measurements are being supplemented by remote sensing from Earth orbit of energetic neutral atom emission from this boundary region by NASA's Interstellar Boundary Explorer (IBEX). Although the Voyagers long ago passed the region of the Classical Kuiper Belt, the New Horizons spacecraft will encounter Pluto in 2015 and thereafter explore one or more KBOs, meanwhile providing updated measurements of the heliospheric radiation environment in this region. Modeling of ion transport within the heliosphere allows specification of time-integrated irradiation effects while the combination of Voyager and IBEX data supports projection of the in-situ measurements into interstellar space beyond the heliosheath. Transformation of model ion flux distributions into surface sputtering and volume ionization profiles provides a multi-layer perspective for space weathering impact on the affected icy bodies and may account for some aspects of color and compositional diversity. Other important related factors may include surface erosion and gardening by meteoritic impacts and surface renewal by cryovolcanism. Chemical products of space weathering may contribute to energy resources for the latter.

The nanophase iron mineral(s) in Mars soil

Science.gov (United States)

Banin, A.; Ben-Shlomo, T.; Margulies, L.; Blake, D. F.; Mancinelli, R. L.; Gehring, A. U.

1993-01-01

A series of surface-modified clays containing nanophase (np) iron oxide/oxyhydroxides of extremely small particle sizes, with total iron contents as high as found in Mars soil, were prepared by iron deposition on the clay surface from ferrous chloride solution. Comprehensive studies of the iron mineralogy in these "Mars-soil analogs" were conducted using chemical extractions, solubility analyses, pH and redox, x ray and electron diffractometry, electron microscopic imaging, specific surface area and particle size determinations, differential thermal analyses, magnetic properties characterization, spectral reflectance, and Viking biology simulation experiments. The clay matrix and the procedure used for synthesis produced nanophase iron oxides containing a certain proportion of divalent iron, which slowly converts to more stable, fully oxidized iron minerals. The clay acted as an effective matrix, both chemically and sterically, preventing the major part of the synthesized iron oxides from ripening, i.e., growing and developing larger crystals. The precipitated iron oxides appear as isodiametric or slightly elongated particles in the size range 1-10 nm, having large specific surface area. The noncrystalline nature of the iron compounds precipitated on the surface of the clay was verified by their complete extractability in oxalate. Lepidocrocite (gamma-FeOOH) was detected by selected area electron diffraction. It is formed from a double iron Fe(II)/Fe(III) hydroxy mineral such as "green rust," or ferrosic hydroxide. Magnetic measurements suggested that lepidocrocite converted to the more stable maghemite (gamma-Fe2O3) by mild heat treatment and then to nanophase hematite (alpha-Fe2O3) by extensive heat treatment. After mild heating, the iron-enriched clay became slightly magnetic, to the extent that it adheres to a hand-held magnet, as was observed with Mars soil. The chemical reactivity of the iron-enriched clays strongly resembles, and offers a plausible mechanism

Trace contaminant concentration affects mineral transformation and pollutant fate in hydroxide-weathered Hanford sediments

International Nuclear Information System (INIS)

Perdrial, Nicolas; Rivera, Nelson; Thompson, Aaron; O’Day, Peggy A.; Chorover, Jon

2011-01-01

Highlights: ► Fate of Sr, Cs and I tracked during hydroxide-weathering of sediments. ► pCO 2 and contaminant concentration affected mineral transformation. ► Sodalite/cancrinite formed at μM levels, chabazite at mM levels. ► Absence of CO 2 resulted in calcite dissolution and strätlingite formation. ► Trace contaminant concentrations modified their own sequestration path. - Abstract: Prior work has shown that when silicaceous sediments are infused with caustic radioactive waste, contaminant fate is tightly coupled to ensuing mineral weathering reactions. However, the effects of local aqueous geochemical conditions on these reactions are poorly studied. Thus, we varied contaminant concentration and pCO 2 during the weathering of previously uncontaminated Hanford sediments over 6 months and 1 year in a solution of caustic waste (pH 13, high ionic strength). Co-contaminants Sr, Cs and I were added at “low” (Cs/Sr: 10 −5 m; I: 10 −7 m) and “high” (Cs/Sr: 10 −3 m; I: 10 −5 m) concentrations, and headspace was held at atmospheric or undetectable ( 2 partial pressure. Solid phase characterization revealed the formation of the zeolite chabazite in “high” samples, whereas feldspathoids, sodalite and cancrinite, were formed preferentially in “low” samples. Sr, Cs and I were sequestered in all reacted sediments. Native calcite dissolution in the CO 2 -free treatment drove the formation of strätlingite (Ca 2 Al 2 SiO 7 ·8H 2 O) and diminished availability of Si and Al for feldspathoid formation. Results indicate that pCO 2 and contaminant concentrations strongly affect contaminant speciation in waste-weathered sediments, and are therefore likely to impact reaction product stability under any remediation scenario.

Influence of pH during chemical weathering of bricks: Long term exposure

DEFF Research Database (Denmark)

Rörig-Dalgaard, Inge; Charola, A. Elena

2016-01-01

Within the framework of environmental weathering of bricks in historical structures, this study focuses on new bricks currently employed for restoration projects. The bricks were subjected to an accelerated chemical weathering test by immersion in solutions with pH ranging from 3 to 13 for differ...

Historical Weathering Based on Chemical Analyses of Two Spodosols in Southern Sweden

International Nuclear Information System (INIS)

Melkerud, Per-Arne; Bain, Derek C.; Olsson, Mats T.

2003-01-01

Chemical weathering losses were calculated for two conifer stands in relation to ongoing studies on liming effects and ash amendments on chemical status, soil solution chemistry and soil genesis. Weathering losses were based on elemental depletion trends in soil profiles since deglaciation and exposure to the weathering environment. Gradients in total geochemical composition were assumed to reflect alteration over time. Study sites were Horroed and Hassloev in southern Sweden. Both Horroed and Hassloev sites are located on sandy loamy Weichselian till at an altitude of 85 and 190 m a.s.l., respectively. Aliquots from volume determined samples from a number of soil levels were fused with lithium metaborate, dissolved in HNO 3 , and analysed by ICP - AES. Results indicated highest cumulative weathering losses at Hassloev. The weathering losses for the elements are in the following order:Si > Al > K > Na > Ca > MgTotal annual losses for Ca+Mg+K+Na, expressed in mmol c m -2 yr -1 , amounted to c. 28 and 58 at Horroed and Hassloev, respectively. Variations between study sites could not be explained by differences in bulk density, geochemistry or mineralogy. The accumulated weathering losses since deglaciation were larger in the uppermost 15 cm than in deeper B horizons for most elements studied

Burkholderia susongensis sp. nov., a mineral-weathering bacterium isolated from weathered rock surface.

Science.gov (United States)

Gu, Jia-Yu; Zang, Sheng-Gang; Sheng, Xia-Fang; He, Lin-Yan; Huang, Zhi; Wang, Qi

2015-03-01

A novel type of mineral-weathering bacterium was isolated from the weathered surface of rock (mica schist) collected from Susong (Anhui, China). Cells of strain L226(T) were Gram-stain-negative. The strain grew optimally at 30 °C, with 1 % (w/v) NaCl and at pH 7.0 in trypticase soy broth. On the basis of 16S rRNA gene phylogeny, strain L226(T) was shown to belong to the genus Burkholderia and the closest phylogenetic relatives were Burkholderia sprentiae WSM5005(T) (98.3 %), Burkholderia acidipaludis NBRC 101816(T) (98.2 %), Burkholderia tuberum STM678(T) (97.2 %) and Burkholderia diazotrophica JPY461(T) (97.1 %). The DNA G+C content was 63.5 mol% and the respiratory quinone was Q-8. The major fatty acids were C16 : 0, C17 : 0 cyclo and C19 : 0 cyclo ω8c. The polar lipid profile of strain L226(T) consisted of a mixture of phosphatidylethanolamine, phosphatidylglycerol, diphosphatidylglycerol, unknown lipids and unidentified aminophospholipids. Based on the low level of DNA-DNA relatedness (ranging from 25.8 % to 34.4 %) to the tested type strains of species of the genus Burkholderia and unique phenotypic characteristics, it is suggested that strain L226(T) represents a novel species of the genus Burkholderia, for which the name Burkholderia susongensis sp. nov., is proposed. The type strain is L226(T) ( = CCTCC AB2014142(T) = JCM 30231(T)). © 2015 IUMS.

A reactive transport model for Marcellus shale weathering

Science.gov (United States)

Heidari, Peyman; Li, Li; Jin, Lixin; Williams, Jennifer Z.; Brantley, Susan L.

2017-11-01

Shale formations account for 25% of the land surface globally and contribute a large proportion of the natural gas used in the United States. One of the most productive shale-gas formations is the Marcellus, a black shale that is rich in organic matter and pyrite. As a first step toward understanding how Marcellus shale interacts with water in the surface or deep subsurface, we developed a reactive transport model to simulate shale weathering under ambient temperature and pressure conditions, constrained by soil and water chemistry data. The simulation was carried out for 10,000 years since deglaciation, assuming bedrock weathering and soil genesis began after the last glacial maximum. Results indicate weathering was initiated by pyrite dissolution for the first 1000 years, leading to low pH and enhanced dissolution of chlorite and precipitation of iron hydroxides. After pyrite depletion, chlorite dissolved slowly, primarily facilitated by the presence of CO2 and organic acids, forming vermiculite as a secondary mineral. A sensitivity analysis indicated that the most important controls on weathering include the presence of reactive gases (CO2 and O2), specific surface area, and flow velocity of infiltrating meteoric water. The soil chemistry and mineralogy data could not be reproduced without including the reactive gases. For example, pyrite remained in the soil even after 10,000 years if O2 was not continuously present in the soil column; likewise, chlorite remained abundant and porosity remained small if CO2 was not present in the soil gas. The field observations were only simulated successfully when the modeled specific surface areas of the reactive minerals were 1-3 orders of magnitude smaller than surface area values measured for powdered minerals. Small surface areas could be consistent with the lack of accessibility of some fluids to mineral surfaces due to surface coatings. In addition, some mineral surface is likely interacting only with equilibrated pore

Evaluating the influence of chemical weathering on the composition of the continental crust using lithium and its isotopes

Science.gov (United States)

Rudnick, R. L.; Liu, X.

2011-12-01

The continental crust has an "intermediate" bulk composition that is distinct from primary melts of peridotitic mantle (basalt or picrite). This mismatch between the "building blocks" and the "edifice" of the continental crust points to the operation of processes that preferentially remove mafic to ultramafic material from the continents. Such processes include lower crustal recycling (via density foundering or lower crustal subduction - e.g., relamination, Hacker et al., 2011, EPSL), generation of evolved melts via slab melting, and/or chemical weathering. Stable isotope systems document the influence of chemical weathering on the bulk crust composition: the oxygen isotope composition of the bulk crust is distinctly heavier than that of primary, mantle-derived melts (Simon and Lecuyer, 2005, G-cubed) and the Li isotopic composition of the bulk crust is distinctly lighter than that of mantle-derive melts (Teng et al., 2004, GCA; 2008, Chem. Geol.). Both signatures mark the imprint of chemical weathering on the bulk crust composition. Here, we use a simple mass balance model for lithium inputs and outputs from the continental crust to quantify the mass lost due to chemical weathering. We find that a minimum of 15%, a maximum of 60%, and a best estimate of ~40% of the original juvenile rock mass may have been lost via chemical weathering. The accumulated percentage of mass loss due to chemical weathering leads to an average global chemical weathering rate (CWR) of ~ 8×10^9 to 2×10^10 t/yr since 3.5 Ga, which is about an order of magnitude higher than the minimum estimates based on modern rivers (Gaillardet et al., 1999, Chem. Geol.). While we cannot constrain the exact portion of crustal mass loss via chemical weathering, given the uncertainties of the calculation, we can demonstrate that the weathering flux is non-zero. Therefore, chemical weathering must play a role in the evolution of the composition and mass of the continental crust.

COST ES0602: towards a European network on chemical weather forecasting and information systems

Directory of Open Access Journals (Sweden)

J. Kukkonen

2009-04-01

Full Text Available The COST ES0602 action provides a forum for benchmarking approaches and practices in data exchange and multi-model capabilities for chemical weather forecasting and near real-time information services in Europe. The action includes approximately 30 participants from 19 countries, and its duration is from 2007 to 2011 (http://www.chemicalweather.eu/. Major efforts have been dedicated in other actions and projects to the development of infrastructures for data flow. We have therefore aimed for collaboration with ongoing actions towards developing near real-time exchange of input data for air quality forecasting. We have collected information on the operational air quality forecasting models on a regional and continental scale in a structured form, and inter-compared and evaluated the physical and chemical structure of these models. We have also constructed a European chemical weather forecasting portal that includes links to most of the available chemical weather forecasting systems in Europe. The collaboration also includes the examination of the case studies that have been organized within COST-728, in order to inter-compare and evaluate the models against experimental data. We have also constructed an operational model forecasting ensemble. Data from a representative set of regional background stations have been selected, and the operational forecasts for this set of sites will be inter-compared and evaluated. The Action has investigated, analysed and reviewed existing chemical weather information systems and services, and will provide recommendations on best practices concerning the presentation and dissemination of chemical weather information towards the public and decision makers.

Hydrologic exchange and chemical weathering in a proglacial watershed near Kangerlussuaq, west Greenland

Science.gov (United States)

Deuerling, Kelly M.; Martin, Jonathan B.; Martin, Ellen E.; Scribner, Cecilia A.

2018-01-01

The exchange of proglacial river water with active layer pore water could alter water chemical compositions in glacial outwash plains and oceanic solute fluxes. To evaluate effects of this exchange, we sampled Watson River and adjacent pore water during the 2013 melt season at two sandurs in western Greenland; one in Sandflugtdalen and the other near the confluence with Søndre Strømfjord. We measured temperature, specific conductivity, and head gradients between the river and bank over a week-long period at Sandflugtdalen, as well as sediment hydraulic conductivity and chemical compositions of waters from both sites. Specific conductivity of pore water is four to ten times greater than river water as solutes are concentrated from weathering reactions, cryoconcentration, and evaporation. Pore water compositions are predominantly altered by carbonate dissolution and sulfide mineral oxidation. High concentrations of HCO3 and SO4 result from solute recycling and dissolution of secondary Ca-Mg carbonate/sulfate salts initially formed by near-surface evaporation in the summer and at depth by freeze-in of the active layer and cryoconcentration in the winter. High hydraulic conductivity (10-5 to 10-4 m/s) and diurnal fluctuations of river stage during our study caused exchange of river and pore water immediately adjacent to the river channel, with a net loss of river water to the bank. Pore water >6 m from the river continuously flowed away from the river. Approximately 1-8% of the river discharge through the Sandflugtdalen was lost to the river bank during our 6.75 day study based on calculations using Darcy's Law. Although not sampled, some of this water should discharge to the river during low river stage early and late in the melt season. Elevated pore water solute concentrations in sandurs and water exchange at diurnal and seasonal frequency should impact fluxes of solutes to the ocean, although understanding the magnitude of this effect will require long

Biotite weathering in a natural forest setting near Derome, Sweden

Science.gov (United States)

Balogh-Brunstad, Z.; Negrich, K.; Hassenkam, T.; Wallander, H.; Stipp, S. L.

2011-12-01

Chemical weathering is a key process in non-nitrogen nutrient acquisition by microbes, fungi and plants. Biotite is commonly the major source of potassium, magnesium and iron. A unique opportunity arose to study natural weathering of biotite by mixed conifer and hardwood forest vegetation and associated microbes and fungi at an abandoned mine site. After the mining stopped over 30 years ago biotite was left behind in piles and the forest vegetation progressively colonized the site. Samples were collected from the top 40 cm of the biotite piles in a vicinity of pine, spruce and birch trees and included some young seedlings. Macroscopic observations documented abundant hyphal growth between the sheets of biotite. We hypothesized that fungal hyphae grow between the sheets to explore the nutrient source and weather the biotite leaving hyphal-sized etched channels on the basal surfaces. Biotite surfaces were examined with atomic force microscopy (AFM) and environmental scanning electron microscopy (ESEM) in their natural state and after removing the biological material from the mineral surfaces. The ESEM images show extensive hyphal colonization and patchy biofilm cover of the entire biotite surface on and within the sheets and at the edges of the particles. Fungal hyphae did not attach strongly to the basal surfaces of the biotite flakes as a result of small particles on the surfaces and the uneven micro-topography. The AFM images illustrate a complex microbial community around the fungal hyphae and detailed fungal morphology. High resolution AFM images show unique globular features of diameter 10-100 nm on all biofilm surfaces. However, removal of the biological material resulted in smooth and un-etched surfaces indicating that either our removal techniques are too invasive and destroy the surface layers of interest, or the etching of the basal surface is not the main mechanism for chemical weathering and base-cation nutrient immobilization in this natural setting

Weathering of the New Albany Shale, Kentucky: II. Redistribution of minor and trace elements

Science.gov (United States)

Tuttle, M.L.W.; Breit, G.N.; Goldhaber, M.B.

2009-01-01

During weathering, elements enriched in black shale are dispersed in the environment by aqueous and mechanical transport. Here a unique evaluation of the differential release, transport, and fate of Fe and 15 trace elements during progressive weathering of the Devonian New Albany Shale in Kentucky is presented. Results of chemical analyses along a weathering profile (unweathered through progressively weathered shale to soil) describe the chemically distinct pathways of the trace elements and the rate that elements are transferred into the broader, local environment. Trace elements enriched in the unweathered shale are in massive or framboidal pyrite, minor sphalerite, CuS and NiS phases, organic matter and clay minerals. These phases are subject to varying degrees and rates of alteration along the profile. Cadmium, Co, Mn, Ni, and Zn are removed from weathered shale during sulfide-mineral oxidation and transported primarily in aqueous solution. The aqueous fluxes for these trace elements range from 0.1 g/ha/a (Cd) to 44 g/ha/a (Mn). When hydrologic and climatic conditions are favorable, solutions seep to surface exposures, evaporate, and form Fe-sulfate efflorescent salts rich in these elements. Elements that remain dissolved in the low pH (pH. Neutralization of the weathering solution in local streams results in elements being adsorbed and precipitated onto sediment surfaces, resulting in trace element anomalies. Other elements are strongly adsorbed or structurally bound to solid phases during weathering. Copper and U initially are concentrated in weathering solutions, but become fixed to modern plant litter in soil formed on New Albany Shale. Molybdenum, Pb, Sb, and Se are released from sulfide minerals and organic matter by oxidation and accumulate in Fe-oxyhydroxide clay coatings that concentrate in surface soil during illuviation. Chromium, Ti, and V are strongly correlated with clay abundance and considered to be in the structure of illitic clay. Illite

Geochemistry of radioactive elements in the process of weathering of carbonatites, acidic and alkali rocks

International Nuclear Information System (INIS)

Zhmodik, S.M.

1984-01-01

Geochemical peculiarities of uranium and thorium behaviour under formation of area crusts of weathering of granitoids, alkali rocks and carbonatites of certain areas of East Siberia are considered. The presented crysts of weathering have been formed under different climatic conditions, they have different age (in the limit of upper Cretaceous period - Neogene up to Quaternary time), chemical and mineral composition. Factors determining and controlling the level of uranium and thorium concentrations in weathering products are disclosed on the basis of facts using the methods of neutron-fragmentary radiography and by-fractional balances. Uranium and thorium distribution in granulometric fractions of crysts of weathering is considered in detail. Data on change in forms of radioactive elements under weathering, effect of fine-dispersed hypergene minerals (kaolinite, montmorillonite, goethite, etc.) on the character of uranium and thorium distribution in eluvial products as well as on sources of migrating uranium in crusts of weathering are presented. Scales of uranium and thorium redistribution under weathering are revealed. Supposition on the source of uranium and throium in sediments is made

Interplay between black carbon and minerals contributes to long term carbon stabilization and mineral transformation

Science.gov (United States)

Liang, B.; Weng, Y. T.; Wang, C. C.; Chiang, C. C.; Liu, C. C.; Lehmann, J.

2017-12-01

Black carbon receives increasing global wide research attention due to its role in carbon sequestration, soil fertility enhancement and remediation application. Generally considered chemically stable in bulk, the reactive surface of BC can interplays with minerals and form strong chemical bondage, which renders physical protection of BC and contributes to its long term stabilization. Using historical BC-rich Amazonian Dark Earth (ADE), we probe the in-situ organo-mineral association and transformation of BC and minerals over a millennium scale using various synchrotron-based spectroscopic (XANES, FTIR) and microscopic (TXM) methods. Higher content of SRO minerals was found in BC-rich ADE compare to adjacent tropical soils. The iron signature found in BC-rich ADE was mainly ferrihydrite/lepidocrocite, a more reactive form of Fe compared to goethite, which was dominant in adjacent soil. Abundant nano minerals particles were observed in-situ associated with BC surface, in clusters and layers. The organo-mineral interaction lowers BC bioavailability and enhances its long-term stabilization in environment, while at the same time, transforms associated minerals into more reactive forms under rapid redox/weathering environment. The results suggest that mineral physical protection for BC sequestration may be more important than previous understanding. The scale up application of BC/biochar into agricultural systems and natural environments have long lasting impact on the in-situ transformation of associated minerals.

Quantifying elemental compositions of primary minerals from granitic rocks and saprolite within the Santa Catalina Mountain Critical Zone Observatory

Science.gov (United States)

Lybrand, R. A.; Rasmussen, C.

2011-12-01

Granitic terrain comprises a significant area of the earth's land surface (>15%). Quantifying weathering processes involved in the transformation of granitic rock to saprolite and soil is central to understanding landscape evolution in these systems. The quantification of primary mineral composition is important for assessing subsequent mineral transformations and soil production. This study focuses on coupling detailed analysis of primary mineral composition to soil development across an array of field sites sampled from the Santa Catalina Mountain Critical Zone observatory (SCM-CZO) environmental gradient. The gradient spans substantial climate-driven shifts in vegetation, ranging from desert scrub to mixed conifer forests. The parent material is a combination of Precambrian and Tertiary aged granites and quartz diorite. Primary mineral type and composition are known to vary among the various aged granitic materials and this variability is hypothesized to manifest as significant variation in regolith forming processes across the SCM-CZO. To address this variability, the mineral composition and mineral formulae of rock and saprolite samples were determined by electron microprobe chemical analyses. The rocks were pre-dominantly quartz, biotite, muscovite, orthoclase and calcium/sodium-rich plagioclase feldspars. Trace minerals observed in the samples included sphene, rutile, zircon, garnet, ilmenite, and apatite. Mineral formulae from electron microprobe analyses were combined with quantitative x-ray diffraction (QXRD) and x-ray fluorescence (XRF) data to quantify both primary and secondary mineralogical components in soil profiles from each of the field sites. Further, electron microprobe analyses of <2mm mixed conifer saprolite revealed weathered plagioclase grains coated with clay-sized particles enriched in silica and aluminum (~25% and 15%, respectively), suggesting kaolin as the secondary phase. The coatings were interspersed within each plagioclase grain, a

The Mineralosphere Concept: Mineralogical Control of the Distribution and Function of Mineral-associated Bacterial Communities.

Science.gov (United States)

Uroz, Stephane; Kelly, Laura Catherine; Turpault, Marie-Pierre; Lepleux, Cendrella; Frey-Klett, Pascale

2015-12-01

Soil is composed of a mosaic of different rocks and minerals, usually considered as an inert substrata for microbial colonization. However, recent findings suggest that minerals, in soils and elsewhere, favour the development of specific microbial communities according to their mineralogy, nutritive content, and weatherability. Based upon recent studies, we highlight how bacterial communities are distributed on the surface of, and in close proximity to, minerals. We also consider the potential role of the mineral-associated bacterial communities in mineral weathering and nutrient cycling in soils, with a specific focus on nutrient-poor and acidic forest ecosystems. We propose to define this microbial habitat as the mineralosphere, where key drivers of the microbial communities are the physicochemical properties of the minerals. Copyright © 2015 Elsevier Ltd. All rights reserved.

The Evolution of Porosity During Weathering of Serpentinite and the Creation of Thin Regolith in the Appalachian Piedmont

Science.gov (United States)

Marcon, V.; Gu, X.; Brantley, S. L.

2017-12-01

Life on Earth relies on the breakdown of impermeable bedrock into porous weathered rock to release nutrients and open pathways for gases and fluids to move through the subsurface. Serpentinites, though rare, are found across the globe and often have thin soils. Few studies have evaluated how porosity, a first order control on weathering, evolves from unweathered serpentinite bedrock to the soil. In this study, we evaluated weathering of serpentinites from bedrock to soil along a ridgetop in Nottingham Park, PA. A suite of geochemical analyses were used to determine chemical and physical changes during weathering. We used neutron scattering to measure pores 2nm to 20 microns in size (referred to here as nanoporosity). As this serpentinite weathers, small pores ( 1nm in diameter) are occluded and total nanoporosity and pore connectivity decrease throughout the weathered rock. Specifically, total nanoporosity decreases from 10% in the unweathered parent material to 5% in the weathered rock. However, in the upper meter of the profile, total nanoporosity increases as Fe, Mg, Mn, Si, Ni, Cr, and V are depleted. Additionally, bulk density and strain calculations suggest total volume expansion throughout the weathered rock followed by volume collapse in the upper 0.5m of the profile. We propose that low temperature reactions alter olivine in the parent material to serpentine minerals at the parent-weathered rock interface, resulting in a volume expansion and the loss of nanopores 1-100nm in size in this weathered rock zone. Volume expansion has long been reported to occur during low temperature serpentinization. We also infer that this loss of porosity limits the infiltration of reactive meteoric fluids into the deeper rock material and restricts the depth of regolith development. Following low temperature serpentinization, serpentine minerals (e.g. antigorite and lizardite) dissolve higher in the weathered rock. Because serpentinite rocks lack a non-reactive mineral such

Elevated olivine weathering rates and sulfate formation at cryogenic temperatures on Mars.

Science.gov (United States)

Niles, Paul B; Michalski, Joseph; Ming, Douglas W; Golden, D C

2017-10-17

Large Hesperian-aged (~3.7 Ga) layered deposits of sulfate-rich sediments in the equatorial regions of Mars have been suggested to be evidence for ephemeral playa environments. But early Mars may not have been warm enough to support conditions similar to what occurs in arid environments on Earth. Instead cold, icy environments may have been widespread. Under cryogenic conditions sulfate formation might be blocked, since kinetics of silicate weathering are typically strongly retarded at temperatures well below 0 °C. But cryo-concentration of acidic solutions may counteract the slow kinetics. Here we show that cryo-concentrated acidic brines rapidly chemically weather olivine minerals and form sulfate minerals at temperatures as low as -60 °C. These experimental results demonstrate the viability of sulfate formation under current Martian conditions, even in the polar regions. An ice-hosted sedimentation and weathering model may provide a compelling description of the origin of large Hesperian-aged layered sulfate deposits on Mars.

Use of Sr isotopes as a tool to decipher the soil weathering processes in a tropical river catchment, southwestern India

International Nuclear Information System (INIS)

Gurumurthy, G.P.; Balakrishna, K.; Tripti, M.; Riotte, Jean; Audry, Stéphane; Braun, Jean-Jacques; Udaya Shankar, H.N.

2015-01-01

River water composition (major ion and "8"7Sr/"8"6Sr ratio) was monitored on a monthly basis over a period of three years from a mountainous river (Nethravati River) of southwestern India. The total dissolved solid (TDS) concentration is relatively low (46 mg L"−"1) with silica being the dominant contributor. The basin is characterised by lower dissolved Sr concentration (avg. 150 nmol L"−"1), with radiogenic "8"7Sr/"8"6Sr isotopic ratios (avg. 0.72041 at outlet). The composition of Sr and "8"7Sr/"8"6Sr and their correlation with silicate derived cations in the river basin reveal that their dominant source is from the radiogenic silicate rock minerals. Their composition in the stream is controlled by a combination of physical and chemical weathering occurring in the basin. The molar ratio of SiO_2/Ca and "8"7Sr/"8"6Sr isotopic ratio show strong seasonal variation in the river water, i.e., low SiO_2/Ca ratio with radiogenic isotopes during non-monsoon and higher SiO_2/Ca with less radiogenic isotopes during monsoon season. Whereas, the seasonal variation of Rb/Sr ratio in the stream water is not significant suggesting that change in the mineral phase being involved in the weathering reaction could be unlikely for the observed molar SiO_2/Ca and "8"7Sr/"8"6Sr isotope variation in river water. Therefore, the shift in the stream water chemical composition could be attributed to contribution of ground water which is in contact with the bedrock (weathering front) during non-monsoon and weathering of secondary soil minerals in the regolith layer during monsoon. The secondary soil mineral weathering leads to limited silicate cation and enhanced silica fluxes in the Nethravati river basin. - Highlights: • Systematic monthly geochemical monitoring of a mountainous tropical river. • Soil weathering has dominant control on the surface water chemistry in the basin. • Soil redox process plays a dominant role in leaching of soil minerals. • Soil mineral weathering in

Impact of landsliding on chemical weathering in the volcanic island of Reunion

Science.gov (United States)

Gayer, E.; Lucas, A.; Bouchez, J.; Sy, A.; Louvat, P.; Gaillardet, J.; Dosseto, A.; Kuessner, M.; Michon, L.; Yokochi, R.

2017-12-01

Tropical precipitation regimes allow for strong erosion that creates dramatic landscapes. Understanding and quantifying erosion processes in tropical volcanic islands is important for both scientific challenges (e.g. regarding their implications for global biogeochemical cycles and their links with climate) and societal matters (e.g. socio-economic and ecosystem damages in highly populated areas). Despite the fact that the link between chemical weathering and physical erosion has long been studied, most research has focused on active mountain ranges. Here we use Reunion Island as a natural laboratory to explore this link in a tectonically inactive environment.In Reunion, estimates show that intense erosion rates are mainly due to stochastic bedrock landsliding. Although landslides affect only a small portion of the landscape they supply rivers with huge amounts of fresh broken rocks and organic matter, which are then available for chemical alteration and for transport. In this study, we measured water chemistry of several streams in Reunion and of landslide seepage water sampled on 2 majors landslides ("Grand Éboulis" and "Mahavel", both > 50 yrs old). Seepage samples from Grand Éboulis show high Total Dissolved Solids (TDS) compared to local streams, in agreement with previous observations showing that landslides promote chemical weathering [1]. However, the low TDS of the Mahavel seep water samples compared to local streams, suggest that the impact of landslides on weathering fluxes may strongly depend on the rate at which landslide debris are transferred downstream and their subsequent residence time in the catchment. In order to calculate such sediment transfer rates in Mahavel, we developed an automated photogrammetric workflow allowing for deriving Digital Elevation Models from historical aerial photos. Using the 30 years of images archived at the Institut Geographique National (5 campaigns), we will be able to delineate the extent of landslide debris, to

77 FR 56717 - Specifications for Medical Examinations of Underground Coal Miners

Science.gov (United States)

2012-09-13

... CFR Part 37 Specifications for Medical Examinations of Underground Coal Miners; Final Rule #0;#0... 0920-AA21 Specifications for Medical Examinations of Underground Coal Miners AGENCY: Centers for... medical examinations of underground coal miners. Existing regulations established specifications for...

Mapping Weathering and Alteration Minerals in the Comstock and Geiger Grade Areas using Visible to Thermal Infrared Airborne Remote Sensing Data

Science.gov (United States)

Vaughan, Greg R.; Calvin, Wendy M.

2005-01-01

To support research into both precious metal exploration and environmental site characterization a combination of high spatial/spectral resolution airborne visible, near infrared, short wave infrared (VNIR/SWIR) and thermal infrared (TIR) image data were acquired to remotely map hydrothermal alteration minerals around the Geiger Grade and Comstock alteration regions, and map the mineral by-products of weathered mine dumps in Virginia City. Remote sensing data from the Airborne Visible Infrared Imaging Spectrometer (AVIRIS), SpecTIR Corporation's airborne hyperspectral imager (HyperSpecTIR), the MODIS-ASTER airborne simulator (MASTER), and the Spatially Enhanced Broadband Array Spectrograph System (SEBASS) were acquired and processed into mineral maps based on the unique spectral signatures of image pixels. VNIR/SWIR and TIR field spectrometer data were collected for both calibration and validation of the remote data sets, and field sampling, laboratory spectral analyses and XRD analyses were made to corroborate the surface mineralogy identified by spectroscopy. The resulting mineral maps show the spatial distribution of several important alteration minerals around each study area including alunite, quartz, pyrophyllite, kaolinite, montmorillonite/muscovite, and chlorite. In the Comstock region the mineral maps show acid-sulfate alteration, widespread propylitic alteration and extensive faulting that offsets the acid-sulfate areas, in contrast to the larger, dominantly acid-sulfate alteration exposed along Geiger Grade. Also, different mineral zones within the intense acid-sulfate areas were mapped. In the Virginia City historic mining district the important weathering minerals mapped include hematite, goethite, jarosite and hydrous sulfate minerals (hexahydrite, alunogen and gypsum) located on mine dumps. Sulfate minerals indicate acidic water forming in the mine dump environment. While there is not an immediate threat to the community, there are clearly sources of

Experimental Acid Weathering of Fe-Bearing Mars Analog Minerals and Rocks: Implications for Aqueous Origin of Hematite-Bearing Sediments in Meridiani Planum, Mars

Science.gov (United States)

Golden, D. C.; Koster, A. M.; Ming, D. W.; Morris, R. V.; Mertzman, S. A.

2011-01-01

A working hypothesis for Meridiani evaporite formation involves the evaporation of fluids derived from acid weathering of Martian basalts and subsequent diagenesis [1, 2]. However, there are no reported experimental studies for the formation of jarosite and gray hematite (spherules), which are characteristic of Meridiani rocks from Mars analog precursor minerals. A terrestrial analog for hematite spherule formation from basaltic rocks under acidic hydrothermal conditions has been reported [3], and we have previously shown that the hematite spherules and jarosite can be synthetically produced in the laboratory using Fe3+ -bearing sulfate brines under hydrothermal conditions [4]. Here we expand and extend these studies by reacting Mars analog minerals with sulfuric acid to form Meridiani-like rock-mineral compositions. The objective of this study is to provide environmental constraints on past aqueous weathering of basaltic materials on Mars.

Mineralogical and geochemical characterization of weathering profiles developed on mylonites in the Fodjomekwet-Fotouni section of the Cameroon Shear Zone (CSZ), West Cameroon

Science.gov (United States)

Tematio, P.; Tchaptchet, W. T.; Nguetnkam, J. P.; Mbog, M. B.; Yongue Fouateu, R.

2017-07-01

The mineralogical and geochemical investigation of mylonitic weathering profiles in Fodjomekwet-Fotouni was done to better trace the occurrence of minerals and chemical elements in this area. Four representative soil profiles were identified in two geomorphological units (upland and lowland) differentiating three weathering products (organo-mineral, mineral and weathered materials). Weathering of these mylonites led to some minerals association such as vermiculite, kaolinite, goethite, smectite, halloysite, phlogopite and gibbsite. The minerals in a decreasing order of abundance are: quartz (24.2%-54.8%); kaolinite (8.4%-36.0%); phlogopite (5.5%-21.9%); goethite (7.8%-16.1%); vermiculite (6.7%-15.7%); smectite (10.2%-11.9%); gibbsite (9.0%-11.8%) and halloysite (5.6%-11.5%) respectively. Patterns of chemical elements allow highlighting three behaviors (enriched elements, depleted elements and elements with complex behavior), depending on the landscape position of the profiles. In the upland weathering products, K, Cr and REEs are enriched; Ca, Mg, Na, Mn, Rb, S and Sr are depleted while Si, Al, Fe, Ti, Ba, Co, Cu, Ga, Mo, Nb, Ni, Pb, Sc, V, Y, Zn and Zr portray a complex behavior. Contrarily, the lowland weathering profiles enriched elements are Fe, Ti, Co, Cr, Cu, V, Zr, Pr, Sm, Tb, Dy, Er and Yb; while depleted elements are Ca, Mg, K, Na, Mn, Ba, Ga, S, Sr, Y, Zn, La, Ce and Nd; and Si, Al, Mo, Nb, Ni, Pb, Rb, Sc evidenced complex behaviors. In all the studied weathering products, the REEs fractionation was also noticeable with a landscape-position dependency, showing light REEs (LREEs) enrichment in the upland areas and heavy REEs (HREEs) in lowland areas. SiO2, Al2O3 and Fe2O3 are positively correlated with most of the traces and REEs (Co, Cu, Nb, Ni, Mo, Pb, Sc, V, Zn, Zr, La, Ce, Sm, Tb, Dy, Er, Yb), pointing to the fact that they may be incorporated into newly formed clay minerals and oxides. Ba, Cr, Ga, Rb, S, Sr, Y, Pr and Nd behave like alkalis and

Silica Retention and Enrichment in Open-System Chemical Weathering on Mars

Science.gov (United States)

Yen, A. S.; Ming, D. W.; Gellert, R.; Clark, B. C.; Mittlefehldt, D. W.; Morris, R. V.; Thompson, L. M.; Berger, J.

2015-01-01

Chemical signatures of weathering are evident in the Alpha Particle X-ray Spectrometer (APXS) datasets from Gusev Crater, Meridiani Planum, and Gale Crater. Comparisons across the landing sites show consistent patterns indicating silica retention and/or enrichment in open-system aqueous alteration.

High potential for weathering and climate effects of non-vascular vegetation in the Late Ordovician

Science.gov (United States)

Porada, Philipp; Lenton, Tim; Pohl, Alexandre; Weber, Bettina; Mander, Luke; Donnadieu, Yannick; Beer, Christian; Pöschl, Ulrich; Kleidon, Axel

2017-04-01

Early non-vascular vegetation in the Late Ordovician may have strongly increased chemical weathering rates of surface rocks at the global scale. This could have led to a drawdown of atmospheric CO2 and, consequently, a decrease in global temperature and an interval of glaciations. Under current climatic conditions, usually field or laboratory experiments are used to quantify enhancement of chemical weathering rates by non-vascular vegetation. However, these experiments are constrained to a small spatial scale and a limited number of species. This complicates the extrapolation to the global scale, even more so for the geological past, where physiological properties of non-vascular vegetation may have differed from current species. Here we present a spatially explicit modelling approach to simulate large-scale chemical weathering by non-vascular vegetation in the Late Ordovician. For this purpose, we use a process-based model of lichens and bryophytes, since these organisms are probably the closest living analogue to Late Ordovician vegetation. The model explicitly represents multiple physiological strategies, which enables the simulated vegetation to adapt to Ordovician climatic conditions. We estimate productivity of Ordovician vegetation with the model, and relate it to chemical weathering by assuming that the organisms dissolve rocks to extract phosphorus for the production of new biomass. Thereby we account for limits on weathering due to reduced supply of unweathered rock material in shallow regions, as well as decreased transport capacity of runoff for dissolved weathered material in dry areas. We simulate a potential global weathering flux of 2.8 km3 (rock) per year, which we define as volume of primary minerals affected by chemical transformation. Our estimate is around 3 times larger than today's global chemical weathering flux. Furthermore, chemical weathering rates simulated by our model are highly sensitive to atmospheric CO2 concentration, which implies

Effect of electromagnetic radiation on the physico-chemical properties of minerals

International Nuclear Information System (INIS)

Lopez M, A.; Delgadillo G, J. A.; Vega C, H. R.

2014-08-01

The electromagnetic radiation effect represented by gamma rays was investigated through; chemical analysis, X-ray diffraction (XRD), scanning electron microscopy (Sem) and magnetization when applied at a dose of 0.5704 Gy (0.5704 J/ kg) at a feed relation of 18.40 ± 1.13 mGy/ h., in different minerals; in order to characterize the impact of the same from 137 Cs in the physicochemical properties of these minerals. All the irradiated samples showed chemical stability at this stage undetectable other both in the XRD study and in the images analysis obtained by Sem; and at present almost the same chemical composition as the non-irradiated samples. So the same patterns of X-ray diffraction thereof, show a tendency to slightly lower the intensity of the most representative peaks of each mineral phase, which may be due to a decrease in crystallinity or preferential crystallographic orientation in crystals. In the micrographs analysis obtained by Sem on the irradiated samples, some holes (open pores) present in the particles were observed, mainly chalcopyrite and sphalerite lesser extent, seen this fact may be due to Compton Effect, in the radiation process. In relation to the magnetization property, a variation is obtained in the saturation magnetization (Ms) for the irradiated samples containing iron and more significantly in the chalcopyrite case. Therefore, with the radiation level used; slight changes occurring in the physical properties of minerals, whereas they remained stable chemically. These small changes may represent a signal that electromagnetic radiation applied at higher doses, is a viable option for improving the mineral processing. (author)

The role of mineral elements and other chemical compounds used in balneology: data from double-blind randomized clinical trials

Science.gov (United States)

Morer, Carla; Roques, Christian-François; Françon, Alain; Forestier, Romain; Maraver, Francisco

2017-12-01

The aims of this study were to conduct a systematic literature review on balneotherapy about the specific therapeutic role of mineral elements and other chemical compounds of mineral waters and derivate peloids/muds and to discuss the study methods used to evaluate it (in musculoskeletal conditions). We searched Medline by PubMed using the following key words: "spa therapy" "balneotherapy" "mud" "peloid" "mud pack Therapy" in combination with "randomized controlled trial" "double blind trial." We also reviewed the reference list of articles retrieved by the Medline search. We selected the double-blind randomized clinical trials that assessed the effects of mineral water or mud treatments compared to tap water, attenuated peloid/mud therapy or similar treatments without the specific minerals or chemical compounds of the treatment group ("non-mineral"). We evaluated the internal validity and the quality of the statistical analysis of these trials. The final selection comprised 27 double-blind randomized clinical trials, 20 related to rheumatology. A total of 1118 patients with rheumatological and other musculoskeletal diseases were evaluated in these studies: 552 of knee osteoarthritis, 47 of hand osteoarthritis, 147 chronic low back pain, 308 of reumathoid arthritis, and 64 of osteoporosis; 293 of these participants were assigned to the experimental groups of knee osteoarthritis, 24 in hand osteoarthritis, 82 of low back pain, 152 with reumathoid arthritis, and 32 with osteoporosis. They were treated with mineral water baths and/or mud/peloid (with or without other forms of treatment, like physical therapy, exercise…). The rest were allocated to the control groups; they received mainly tap water and/or "non-mineral" mud/peloid treatments. Mineral water or mud treatments had better and longer improvements in pain, function, quality of life, clinical parameters, and others in some rheumatologic diseases (knee and hand osteoarthritis, chronic low back pain

1.3. Chemical and mineral additives of concretes and water used for concrete mix preparation

International Nuclear Information System (INIS)

Saidov, D.Kh.

2011-01-01

It is known that chemical and mineral additives increase physicochemical properties of concretes, thus, chemical and mineral additives, including super plasticizer and organo mineral additives are examined in this work. It was noted that along with salt water fresh water can also be used for concrete mix preparation.

Experimental weathering rates of aluminium silicates

International Nuclear Information System (INIS)

Gudbrandsson, Snorri

2013-01-01

The chemical weathering of primary rocks and minerals in natural systems has a major impact on soil development and its composition. Chemical weathering is driven to a large extent by mineral dissolution. Through mineral dissolution, elements are released into groundwater and can readily react to precipitate secondary minerals such as clays, zeolites, and carbonates. Carbonates form from divalent cations (e.g. Ca, Fe and Mg) and CO 2 , and kaolin clay and gibbsite formation is attributed to the weathering of aluminium-rich minerals, most notably the feldspars. The CarbFix Project in Hellisheidi (SW-Iceland) aims to use natural weathering processes to form carbonate minerals by the re-injection of CO 2 from a geothermal power plant back into surrounding basaltic rocks. This process is driven by the dissolution of basaltic rocks, rich in divalent cations, which can combine with injected CO 2 to form and precipitate carbonates. This thesis focuses on the dissolution behaviour of Stapafell crystalline basalt, which consists of three major phases (plagioclase, pyroxene, and olivine) and is rich in divalent cations. Steady-state element release rates from crystalline basalt at far-from-equilibrium conditions were measured at pH from 2 to 11 and temperatures from 5 to 75 C in mixed-flow reactors. Steady-state Si and Ca release rates exhibit a U-shaped variation with pH, where rates decrease with increasing pH at acid condition but increase with increasing pH at alkaline conditions. Silicon release rates from crystalline basalt are comparable to Si release rates from basaltic glass of the same chemical composition at low pH and temperatures ≥25 C but slower at alkaline pH and temperatures ≥50 C. In contrast, Mg and Fe release rates decrease continuously with increasing pH at all temperatures. This behaviour is interpreted to stem from the contrasting dissolution behaviours of the three major minerals comprising the basalt: plagioclase, pyroxene, and olivine. Element

A review of operational, regional-scale, chemical weather forecasting models in Europe

Czech Academy of Sciences Publication Activity Database

Kukkonen, J.; Olsson, T.; Schultz, D.M.; Baklanov, A.; Klein, T.; Miranda, A.I.; Monteiro, A.; Hirtl, M.; Tarvainen, V.; Boy, M.; Peuch, V.H.; PoupKou, A.; Kioutsioukis, I.; Finardi, S.; Sofiev, M.; Sokhi, R.; Lehtinen, K.E.J.; Karatzas, K.; San José, R.; Astitha, M.; Kallos, G.; Schaap, M.; Reimer, E.; Jakobs, H.; Eben, Kryštof

2012-01-01

Roč. 12, - (2012), s. 1-87 ISSN 1680-7316 Institutional research plan: CEZ:AV0Z10300504 Keywords : chemical weather * numerical models * operational forecasting * air Subject RIV: DG - Athmosphere Sciences, Meteorology Impact factor: 5.510, year: 2012

Mineral transformation controls speciation and pore-fluid transmission of contaminants in waste-weathered Hanford sediments

Science.gov (United States)

Perdrial, Nicolas; Thompson, Aaron; O'Day, Peggy A.; Steefel, Carl I.; Chorover, Jon

2014-09-01

Portions of the Hanford Site (WA, USA) vadose zone were subjected to weathering by caustic solutions during documented releases of high level radioactive waste (containing Sr, Cs and I) from leaking underground storage tanks. Previous studies have shown that waste-sediment interactions can promote variable incorporation of contaminants into neo-formed mineral products (including feldspathoids and zeolites), but processes regulating the subsequent contaminant release from these phases into infiltrating background pore waters remain poorly known. In this paper, reactive transport experiments were conducted with Hanford sediments previously weathered for one year in simulated hyper-alkaline waste solutions containing high or low 88Sr, 127I, and 133Cs concentrations, with or without CO2(aq). These waste-weathered sediments were leached in flow-through column experiments with simulated background pore water (characteristic of meteoric recharge) to measure contaminant release from solids formed during waste-sediment interaction. Contaminant sorption-desorption kinetics and mineral transformation reactions were both monitored using continuous-flow and wet-dry cycling regimes for ca. 300 pore volumes. Less than 20% of contaminant 133Cs and 88Sr mass and less than 40% 127I mass were released over the course of the experiment. To elucidate molecular processes limiting contaminant release, reacted sediments were studied with micro- (TEM and XRD) and molecular- (Sr K-edge EXAFS) scale methods. Contaminant dynamics in column experiments were principally controlled by rapid dissolution of labile solids and competitive exchange reactions. In initially feldspathoidic systems, time-dependent changes in the local zeolitic bonding environment observed with X-ray diffraction and EXAFS are responsible for limiting contaminant release. Linear combination fits and shell-by-shell analysis of Sr K-edge EXAFS data revealed modification in Sr-Si/Al distances within the zeolite cage. Wet

Strontium stable isotope behaviour accompanying basalt weathering

Science.gov (United States)

Burton, K. W.; Parkinson, I. J.; Gíslason, S. G. R.

2016-12-01

The strontium (Sr) stable isotope composition of rivers is strongly controlled by the balance of carbonate to silicate weathering (Krabbenhöft et al. 2010; Pearce et al. 2015). However, rivers draining silicate catchments possess distinctly heavier Sr stable isotope values than their bedrock compositions, pointing to significant fractionation during weathering. Some have argued for preferential release of heavy Sr from primary phases during chemical weathering, others for the formation of secondary weathering minerals that incorporate light isotopes. This study presents high-precision double-spike Sr stable isotope data for soils, rivers, ground waters and estuarine waters from Iceland, reflecting both natural weathering and societal impacts on those environments. The bedrock in Iceland is dominantly basaltic, d88/86Sr ≈ +0.27, extending to lighter values for rhyolites. Geothermal waters range from basaltic Sr stable compositions to those akin to seawater. Soil pore waters reflect a balance of input from primary mineral weathering, precipitation and litter recycling and removal into secondary phases and vegetation. Rivers and ground waters possess a wide range of d88/86Sr compositions from +0.101 to +0.858. Elemental and isotope data indicate that this fractionation primarily results from the formation or dissolution of secondary zeolite (d88/86Sr ≈ +0.10), but also carbonate (d88/86Sr ≈ +0.22) and sometimes anhydrite (d88/86Sr ≈ -0.73), driving the residual waters to heavier or lighter values, respectively. Estuarine waters largely reflect mixing with seawater, but are also be affected by adsorption onto particulates, again driving water to heavy values. Overall, these data indicate that the stability and nature of secondary weathering phases, exerts a strong control on the Sr stable isotope composition of silicate rivers. [1] Krabbenhöft et al. (2010) Geochim. Cosmochim. Acta 74, 4097-4109. [2] Pearce et al. (2015) Geochim. Cosmochim. Acta 157, 125-146.

Carbon dioxide sequestration by mineral carbonation. Feasibility of enhanced natural weathering as a CO2 emission reduction technology

International Nuclear Information System (INIS)

Huijgen, W.J.J.

2007-01-01

A possible technology that can contribute to the reduction of carbon dioxide emissions is CO2 sequestration by mineral carbonation. The basic concept behind mineral CO2 sequestration is the mimicking of natural weathering processes in which calcium or magnesium containing minerals react with gaseous CO2 and form solid calcium or magnesium carbonates. Potential advantages of mineral CO2 sequestration compared to, e.g., geological CO2 storage include (1) the permanent and inherently safe sequestration of CO2, due to the thermodynamic stability of the carbonate product formed and (2) the vast potential sequestration capacity, because of the widespread and abundant occurrence of suitable feedstock. In addition, carbonation is an exothermic process, which potentially limits the overall energy consumption and costs of CO2 emission reduction. However, weathering processes are slow, with timescales at natural conditions of thousands to millions of years. For industrial implementation, a reduction of the reaction time to the order of minutes has to be achieved by developing alternative process routes. The aim of this thesis is an investigation of the technical, energetic, and economic feasibility of CO2 sequestration by mineral carbonation. In Chapter 1 the literature published on CO2 sequestration by mineral carbonation is reviewed. Among the potentially suitable mineral feedstock for mineral CO2 sequestration, Ca-silicates, more particularly wollastonite (CaSiO3), a mineral ore, and steel slag, an industrial alkaline solid residue, are selected for further research. Alkaline Ca-rich residues seem particularly promising, since these materials are inexpensive and available near large industrial point sources of CO2. In addition, residues tend to react relatively rapidly with CO2 due to their (geo)chemical instability. Various process routes have been proposed for mineral carbonation, which often include a pre-treatment of the solid feedstock (e.g., size reduction and

Structure and chemical characteristics of natural mineral deposit Terbunskaya (Lipetsk region, Russia)

Energy Technology Data Exchange (ETDEWEB)

Motyleva, S., E-mail: motyleva-svetlana@mail.ru; Mertvishcheva, M. [All-Russian Horticular Institute for Breeding, Agrotechnology and Nursery Russian Academy of Agricultural Sciences, Moskow (Russian Federation); Shchuchka, R.; Gulidova, V. [Yelets state university named after I. A. Bunin, Yelets (Russian Federation)

2015-07-22

New knowledge about the mineralogical features Terbunsky mineral. Investigated 5 fractions isolated from the incision (2-2,5 m). Terbunskaya deposit belongs to minerals Santonian age. Scanning electron microscopy and energy dispersive analysis of fractions isolated studied in detail. In the coarse fractions found ancient organic remains of algae and micro-organisms that have been sedimented together with the mineral component during geological periods. The share of organic inclusions does not exceed 1.5%. Chemical composition confirms the presence of silicon and carbonate organisms. Advantageously proportion of minerals having a layered structure with a plurality of micro and nano pore size 600 - 80-nm and an average chemical composition (wt%): Na (0,64), Mg (0,54), Al (13.48), Si (27 57), K (2.39) Ca (0.75)

Testing the control of mineral supply rates on chemical erosion in the Klamath Mountains

Science.gov (United States)

West, N.; Ferrier, K.

2017-12-01

The relationship between rates of chemical erosion and mineral supply is central to many problems in Earth science, including the role of tectonics in the global carbon cycle, nutrient supply to soils and streams via soil production, and lithologic controls on landscape evolution. We aim to test the relationship between mineral supply rates and chemical erosion in the forested uplands of the Klamath mountains, along a latitudinal transect of granodioritic plutons that spans an expected gradient in mineral supply rates associated with the geodynamic response to the migration of the Mendocino Triple Junction. We present 10Be-derived erosion rates and Zr-derived chemical depletion factors, as well as bulk soil and rock geochemistry on 10 ridgetops along the transect to test hypotheses about supply-limited and kinetically-limited chemical erosion. Previous studies in this area, comparing basin-averaged erosion rates and modeled uplift rates, suggest this region may be adjusted to an approximate steady state. Our preliminary results suggest that chemical erosion at these sites is influenced by both mineral supply rates and dissolution kinetics.

Impact of Poultry Litter Cake, Cleanout, and Bedding following Chemical Amendments on Soil C and N Mineralization

Directory of Open Access Journals (Sweden)

Dexter B. Watts

2012-01-01

Full Text Available Poultry litter is a great alternative N source for crop production. However, recent poultry litter management changes, and increased chemical amendment use may impact its N availability. Thus, research was initiated to evaluate the effect that broiler cake and total cleanout litter amended with chemical additives have on C and N mineralization. A 35-day incubation study was carried out on a Hartsells fine sandy loam (fine-loamy, siliceous, subactive, thermic Typic Hapludults soil common to the USA Appalachian Plateau region. Three poultry litter components (broiler cake, total cleanout, and bedding material from a broiler house were evaluated and compared to a soil control. Chemical amendments lime (CaCO3, gypsum (CaSO4, aluminum sulfate (AlSO4, and ferrous sulfate (FeSO4 were added to the poultry litter components to determine their impact on C and N mineralization. Litter component additions increased soil C mineralization in the order of broiler cake > total cleanout > bedding > soil control. Although a greater concentration of organic C was observed in the bedding, broiler cake mineralized the most C, which can be attributed to differences in the C : N ratio between treatments. Chemical amendment in addition to the manured soil also impacted C mineralization, with AlSO4 generally decreasing mineralization. Nitrogen mineralization was also significantly affected by poultry litter component applications. Broiler cake addition increased N availability followed by total cleanout compared to soil control, while the bedding resulted in net N immobilization. Chemical amendments impacted N mineralization primarily in the broiler cake amended soil where all chemical amendments decreased mineralization compared to the no chemical amendment treatment. This short-term study (35-day incubation indicates that N availability to crops may be different depending on the poultry litter component used for fertilization and chemical amendment use which could

Selective detection of Fe and Mn species at mineral surfaces in weathered granite by conversion electron yield X-ray absorption fine structure

International Nuclear Information System (INIS)

Itai, Takaaki; Takahashi, Yoshio; Uruga, Tomoya; Tanida, Hajime; Iida, Atsuo

2008-01-01

A new method for the speciation of Fe and Mn at mineral surfaces is proposed using X-ray absorption fine structure in conversion electron yield mode (CEY-XAFS). This method generally reflects information on the species at the sub-μm scale from the particle surface due to the limited escape depth of the inelastic Auger electron. The surface sensitivity of this method was assessed by experiments on two samples of granite showing different degrees of weathering. The XANES spectra of the Fe-K and Mn-K edge clearly gave different information for CEY and fluorescence (FL) modes. These XANES spectra of Fe and Mn show a good fit upon application of least-squares fitting using ferrihydrite/MnO 2 and biotite as the end members. The XANES spectra collected by CEY mode provided more selective information on the secondary phases which are probably present at the mineral surfaces. In particular, CEY-XANES spectra of Mn indicated the presence of Mn oxide in unweathered granite despite a very small contribution of Mn oxide being indicated by FL-XANES and selective chemical-extraction analyses. Manganese oxide could not be detected by micro-beam XANES (beam size: 5 x 5 μm 2 ) in unweathered granite, suggesting that Mn oxide thinly and ubiquitously coats mineral surface at a sub-μm scale. This information is important, since Mn oxide can be the host for various trace elements. CEY-XAFS can prove to be a powerful tool as a highly sensitive surface speciation method. Combination of CEY and FL-XAFS will help identify minor phases that form at mineral surfaces, but identification of Fe and Mn oxides at mineral surfaces is critical to understand the migration of trace elements in water-rock interaction

Selective detection of Fe and Mn species at mineral surfaces in weathered granite by conversion electron yield X-ray absorption fine structure

Energy Technology Data Exchange (ETDEWEB)

Itai, Takaaki [Department of Earth and Planetary Systems Science, Hiroshima University, Kagamiyama, Higashi-Hiroshima, Hiroshima 739-8526 (Japan)], E-mail: itai-epss@hiroshima-u.ac.jp; Takahashi, Yoshio [Department of Earth and Planetary Systems Science, Hiroshima University, Kagamiyama, Higashi-Hiroshima, Hiroshima 739-8526 (Japan); Uruga, Tomoya; Tanida, Hajime [Japan Synchrotron Radiation Research Institute, 1-1-1 Kouto, Sayo-cho, Sayo-gun, Hyogo 679-5198 (Japan); Iida, Atsuo [Photon Factory, National Laboratory for High Energy Physics, O-ho, Tsukuba, Ibaraki 305 (Japan)

2008-09-15

A new method for the speciation of Fe and Mn at mineral surfaces is proposed using X-ray absorption fine structure in conversion electron yield mode (CEY-XAFS). This method generally reflects information on the species at the sub-{mu}m scale from the particle surface due to the limited escape depth of the inelastic Auger electron. The surface sensitivity of this method was assessed by experiments on two samples of granite showing different degrees of weathering. The XANES spectra of the Fe-K and Mn-K edge clearly gave different information for CEY and fluorescence (FL) modes. These XANES spectra of Fe and Mn show a good fit upon application of least-squares fitting using ferrihydrite/MnO{sub 2} and biotite as the end members. The XANES spectra collected by CEY mode provided more selective information on the secondary phases which are probably present at the mineral surfaces. In particular, CEY-XANES spectra of Mn indicated the presence of Mn oxide in unweathered granite despite a very small contribution of Mn oxide being indicated by FL-XANES and selective chemical-extraction analyses. Manganese oxide could not be detected by micro-beam XANES (beam size: 5 x 5 {mu}m{sup 2}) in unweathered granite, suggesting that Mn oxide thinly and ubiquitously coats mineral surface at a sub-{mu}m scale. This information is important, since Mn oxide can be the host for various trace elements. CEY-XAFS can prove to be a powerful tool as a highly sensitive surface speciation method. Combination of CEY and FL-XAFS will help identify minor phases that form at mineral surfaces, but identification of Fe and Mn oxides at mineral surfaces is critical to understand the migration of trace elements in water-rock interaction.

Colluvial deposits as a possible weathering reservoir in uplifting mountains

Science.gov (United States)

Carretier, Sébastien; Goddéris, Yves; Martinez, Javier; Reich, Martin; Martinod, Pierre

2018-03-01

The role of mountain uplift in the evolution of the global climate over geological times is controversial. At the heart of this debate is the capacity of rapid denudation to drive silicate weathering, which consumes CO2. Here we present the results of a 3-D model that couples erosion and weathering during mountain uplift, in which, for the first time, the weathered material is traced during its stochastic transport from the hillslopes to the mountain outlet. To explore the response of weathering fluxes to progressively cooler and drier climatic conditions, we run model simulations accounting for a decrease in temperature with or without modifications in the rainfall pattern based on a simple orographic model. At this stage, the model does not simulate the deep water circulation, the precipitation of secondary minerals, variations in the pH, below-ground pCO2, and the chemical affinity of the water in contact with minerals. Consequently, the predicted silicate weathering fluxes probably represent a maximum, although the predicted silicate weathering rates are within the range of silicate and total weathering rates estimated from field data. In all cases, the erosion rate increases during mountain uplift, which thins the regolith and produces a hump in the weathering rate evolution. This model thus predicts that the weathering outflux reaches a peak and then falls, consistent with predictions of previous 1-D models. By tracking the pathways of particles, the model can also consider how lateral river erosion drives mass wasting and the temporary storage of colluvial deposits on the valley sides. This reservoir is comprised of fresh material that has a residence time ranging from several years up to several thousand years. During this period, the weathering of colluvium appears to sustain the mountain weathering flux. The relative weathering contribution of colluvium depends on the area covered by regolith on the hillslopes. For mountains sparsely covered by regolith

Hillslope chemical weathering across Paraná, Brazil: A data mining-GIS hybrid approach

Science.gov (United States)

Iwashita, Fabio; Friedel, Michael J.; Filho, Carlos Roberto de Souza; Fraser, Stephen J.

2011-09-01

Self-organizing map (SOM) and geographic information system (GIS) models were used to investigate the nonlinear relationships associated with geochemical weathering processes at local (~100 km 2) and regional (~50,000 km 2) scales. The data set consisted of 1) 22 B-horizon soil variables: P, C, pH, Al, total acidity, Ca, Mg, K, total cation exchange capacity, sum of exchangeable bases, base saturation, Cu, Zn, Fe, B, S, Mn, gammaspectrometry (total count, potassium, thorium, and uranium) and magnetic susceptibility measures; and 2) six topographic variables: elevation, slope, aspect, hydrological accumulated flux, horizontal curvature and vertical curvature. It is characterized at 304 locations from a quasi-regular grid spaced about 24 km across the state of Paraná. This data base was split into two subsets: one for analysis and modeling (274 samples) and the other for validation (30 samples) purposes. The self-organizing map and clustering methods were used to identify and classify the relations among solid-phase chemical element concentrations and GIS derived topographic models. The correlation between elevation and k-means clusters related the relative position inside hydrologic macro basins, which was interpreted as an expression of the weathering process reaching a steady-state condition at the regional scale. Locally, the chemical element concentrations were related to the vertical curvature representing concave-convex hillslope features, where concave hillslopes with convergent flux tends to be a reducing environment and convex hillslopes with divergent flux, oxidizing environments. Stochastic cross validation demonstrated that the SOM produced unbiased classifications and quantified the relative amount of uncertainty in predictions. This work strengthens the hypothesis that, at B-horizon steady-state conditions, the terrain morphometry were linked with the soil geochemical weathering in a two-way dependent process: the topographic relief was a factor on

Hillslope chemical weathering across Paraná, Brazil: a data mining-GIS hybrid approach

Science.gov (United States)

Iwashita, Fabio; Friedel, Michael J.; Filho, Carlos Roberto de Souza; Fraser, Stephen J.

2011-01-01

Self-organizing map (SOM) and geographic information system (GIS) models were used to investigate the nonlinear relationships associated with geochemical weathering processes at local (~100 km2) and regional (~50,000 km2) scales. The data set consisted of 1) 22 B-horizon soil variables: P, C, pH, Al, total acidity, Ca, Mg, K, total cation exchange capacity, sum of exchangeable bases, base saturation, Cu, Zn, Fe, B, S, Mn, gammaspectrometry (total count, potassium, thorium, and uranium) and magnetic susceptibility measures; and 2) six topographic variables: elevation, slope, aspect, hydrological accumulated flux, horizontal curvature and vertical curvature. It is characterized at 304 locations from a quasi-regular grid spaced about 24 km across the state of Paraná. This data base was split into two subsets: one for analysis and modeling (274 samples) and the other for validation (30 samples) purposes. The self-organizing map and clustering methods were used to identify and classify the relations among solid-phase chemical element concentrations and GIS derived topographic models. The correlation between elevation and k-means clusters related the relative position inside hydrologic macro basins, which was interpreted as an expression of the weathering process reaching a steady-state condition at the regional scale. Locally, the chemical element concentrations were related to the vertical curvature representing concave–convex hillslope features, where concave hillslopes with convergent flux tends to be a reducing environment and convex hillslopes with divergent flux, oxidizing environments. Stochastic cross validation demonstrated that the SOM produced unbiased classifications and quantified the relative amount of uncertainty in predictions. This work strengthens the hypothesis that, at B-horizon steady-state conditions, the terrain morphometry were linked with the soil geochemical weathering in a two-way dependent process: the topographic relief was a factor on

Mineralogic sources of metals in leachates from the weathering of sedex, massive sulfide, and vein deposit mining wastes

Science.gov (United States)

Diehl, S.F.; Hageman, P.L.; Seal, R.R.; Piatak, N.M.; Lowers, H.

2011-01-01

Weathered mine waste consists of oxidized primary minerals and chemically unstable secondary phases that can be sources of readily soluble metals and acid rock drainage. Elevated concentrations of metals such as Cd, Cu, Fe, Mn, Ni, Pb, and Zn are observed in deionized water-based leachate solutions derived from complex sedex and Cu-Pb-Zn mine wastes. Leachate (USGS FLT) from the Elizabeth mine, a massive sulfide deposit, has a pH of 3.4 and high concentrations of Al (16700 ug/L), Cu (440 ug/L), and Zn (8620 ug/L). Leachate from the sedex Faro mine has a pH of 3.5 and high concentrations of Al (2040 ug/L), Cu (1930 ug/L), Pb (2080 ug/L), and Zn (52900 ug/L). In contrast, higher-pH leachates produced from tailings of polymetallic vein deposits have order of magnitude lower metal concentrations. These data indicate that highly soluble secondary mineral phases exist at the surface of waste material where the samples were collected. Sulfide minerals from all sites exhibit differential degrees of weathering, from dissolution etched grain rims, to rinds of secondary minerals, to skeletal remnants. These microscale mineral-dissolution textures enhance weathering and metal teachability of waste material. Besides the formation of secondary minerals, sulfide grains from dried tailings samples may be coated by amorphous Fe-Al-Si minerals that also adsorb metals such as Cu, Ni, and Zn.

Formation of halloysite from feldspar: Low temperature, artificial weathering versus natural weathering

Science.gov (United States)

Parham, Walter E.

1969-01-01

Weathering products formed on surfaces of both potassium and plagioclase feldspar (An70), which were continuously leached in a Soxhlet extraction apparatus for 140 days with 7.21 of distilled water per day at a temperature of approximately 78°C, are morphologically identical to natural products developed on potassium feldspars weathered under conditions of good drainage in the humid tropics. The new products, which first appear as tiny bumps on the feldspar surface, start to develop mainly at exposed edges but also at apparently random sites on flat cleavage surfaces. As weathering continues, the bumps grow outward from the feldspar surface to form tapered projections, which then develop into wide-based thin films or sheets. The thin sheets of many projections merge laterally to form one continuous flame-shaped sheet. The sheets formed on potassium feldspars may then roll to form tubes that are inclined at a high angle to the feldspar surface. Etch pits of triangular outline on the artificially weathered potassium feldspars serve as sites for development of continuous, non-rolled, hollow tubes. It is inferred from its morphology that this weathering product is halloysite or its primitive form. The product of naturally weathered potassium feldspars is halloysite . 4H2O.The flame-shaped films or sheets formed on artificially weathered plagioclase feldspar do not develop into hollow tubes, but instead give rise to a platy mineral that is most probably boehmite. These plates form within the flame-shaped films, and with continued weathering are released as the film deteriorates. There is no indication from this experiment that platy pseudohexagonal kaolinite forms from any of these minerals under the initial stage of weathering.

The acid and alkalinity budgets of weathering in the Andes-Amazon system: Insights into the erosional control of global biogeochemical cycles

Science.gov (United States)

Torres, Mark A.; West, A. Joshua; Clark, Kathryn E.; Paris, Guillaume; Bouchez, Julien; Ponton, Camilo; Feakins, Sarah J.; Galy, Valier; Adkins, Jess F.

2016-09-01

The correlation between chemical weathering fluxes and denudation rates suggests that tectonic activity can force variations in atmospheric pCO2 by modulating weathering fluxes. However, the effect of weathering on pCO2 is not solely determined by the total mass flux. Instead, the effect of weathering on pCO2 also depends upon the balance between 1) alkalinity generation by carbonate and silicate mineral dissolution and 2) sulfuric acid generation by the oxidation of sulfide minerals. In this study, we explore how the balance between acid and alkalinity generation varies with tectonic uplift to better understand the links between tectonics and the long-term carbon cycle. To trace weathering reactions across the transition from the Peruvian Andes to the Amazonian foreland basin, we measured a suite of elemental concentrations (Na, K, Ca, Mg, Sr, Si, Li, SO4, and Cl) and isotopic ratios (87Sr/86Sr and δ34S) on both dissolved and solid phase samples. Using an inverse model, we quantitatively link systematic changes in solute geochemistry with elevation to downstream declines in sulfuric acid weathering as well as the proportion of cations sourced from silicates. With a new carbonate-system framework, we show that weathering in the Andes Mountains is a CO2 source whereas foreland weathering is a CO2 sink. These results are consistent with the theoretical expectation that the ratio of sulfide oxidation to silicate weathering increases with increasing erosion. Altogether, our results suggest that the effect of tectonically-enhanced weathering on atmospheric pCO2 is strongly modulated by sulfide mineral oxidation.

Bacterially-mediated weathering of crystalline and amorphous Cu-slags

International Nuclear Information System (INIS)

Potysz, Anna; Grybos, Malgorzata; Kierczak, Jakub; Guibaud, Gilles; Lens, Piet N.L.; Hullebusch, Eric D. van

2016-01-01

Two types of Cu-slags (CS: crystalline massive slag and GS: granulated amorphous slag) exhibiting a different chemical and mineral phase composition were compared with respect to their susceptibility to bacterial weathering using Pseudomonas aeruginosa (n° CIP 105094). Abiotic conditions e.g. sterile growth medium and ultrapure water were used for comparison. The experiments were extended up to 112 days with a systematic liquid phase renewal every 14 days. The results revealed significant release of elements in the bacterially mediated weathering experiments. Concentrations of elements (Si, Fe, Cu, Zn and Pb) in the biotic solutions were increased at least by 20% up to 99% compared to abiotic ones. From 3 to 77% of the leached elements were associated to the fraction >0.22 μm. Scanning electron microscope observations demonstrated greater weathering of mineral phases in biotic experiments than in abiotic ones which is in accordance with the solution chemistry exhibiting higher concentrations of elements leached in biotic set-ups. In the case of CS, glass and sulfides weathering was yet observed in abiotic experiment, whereas partial dissolution of fayalite (Fe_2SiO_4) was solely affected by the presence of bacteria. GS having a higher bulk content of metallic elements was found to be more stable than sulfide-bearing CS, while its (GS) glass matrix was found to weather easier under biotic conditions. - Highlights: • Pseudomonas aeruginosa significantly enhance the release of elements from Cu-slags. • Bacteria and/or associated metabolites assist as biosorbent (e.g. Zn). • Amorphous slag is more susceptible to bio-weathering. • Metal carriers of crystalline slag are prone to dissolution. • Fe-bearing fayalite is altered solely due to the presence of bacteria.

Weather elements, chemical air pollutants and airborne pollen influencing asthma emergency room visits in Szeged, Hungary: performance of two objective weather classifications.

Science.gov (United States)

Makra, László; Puskás, János; Matyasovszky, István; Csépe, Zoltán; Lelovics, Enikő; Bálint, Beatrix; Tusnády, Gábor

2015-09-01

Weather classification approaches may be useful tools in modelling the occurrence of respiratory diseases. The aim of the study is to compare the performance of an objectively defined weather classification and the Spatial Synoptic Classification (SSC) in classifying emergency department (ED) visits for acute asthma depending from weather, air pollutants, and airborne pollen variables for Szeged, Hungary, for the 9-year period 1999-2007. The research is performed for three different pollen-related periods of the year and the annual data set. According to age and gender, nine patient categories, eight meteorological variables, seven chemical air pollutants, and two pollen categories were used. In general, partly dry and cold air and partly warm and humid air aggravate substantially the symptoms of asthmatics. Our major findings are consistent with this establishment. Namely, for the objectively defined weather types favourable conditions for asthma ER visits occur when an anticyclonic ridge weather situation happens with near extreme temperature and humidity parameters. Accordingly, the SSC weather types facilitate aggravating asthmatic conditions if warm or cool weather occur with high humidity in both cases. Favourable conditions for asthma attacks are confirmed in the extreme seasons when atmospheric stability contributes to enrichment of air pollutants. The total efficiency of the two classification approaches is similar in spite of the fact that the methodology for derivation of the individual types within the two classification approaches is completely different.

Links between climate change, water-table depth, and water chemistry in a mineralized mountain watershed

Science.gov (United States)

Manning, Andrew H.; Verplanck, Philip L.; Caine, Jonathan S.; Todd, Andrew S.

2013-01-01

Recent studies suggest that climate change is causing rising solute concentrations in mountain lakes and streams. These changes may be more pronounced in mineralized watersheds due to the sensitivity of sulfide weathering to changes in subsurface oxygen transport. Specific causal mechanisms linking climate change and accelerated weathering rates have been proposed, but in general remain entirely hypothetical. For mineralized watersheds, a favored hypothesis is that falling water tables caused by declining recharge rates allow an increasing volume of sulfide-bearing rock to become exposed to air, thus oxygen. Here, we test the hypothesis that falling water tables are the primary cause of an increase in metals and SO4 (100-400%) observed since 1980 in the Upper Snake River (USR), Colorado. The USR drains an alpine watershed geologically and climatologically representative of many others in mineralized areas of the western U.S. Hydrologic and chemical data collected from 2005 to 2011 in a deep monitoring well (WP1) at the top of the USR watershed are utilized. During this period, both water table depths and groundwater SO4 concentrations have generally increased in the well. A numerical model was constructed using TOUGHREACT that simulates pyrite oxidation near WP1, including groundwater flow and oxygen transport in both saturated and unsaturated zones. The modeling suggests that a falling water table could produce an increase in metals and SO4 of a magnitude similar to that observed in the USR (up to 300%). Future water table declines may produce limited increases in sulfide weathering high in the watershed because of the water table dropping below the depth of oxygen penetration, but may continue to enhance sulfide weathering lower in the watershed where water tables are shallower. Advective air (oxygen) transport in the unsaturated zone caused by seasonally variable recharge and associated water table fluctuations was found to have little influence on pyrite

Chemical evolution of the early Martian hydrosphere

International Nuclear Information System (INIS)

Schaefer, M.W.

1990-01-01

The chemical evolution of the early Martian hydrosphere is discussed. The early Martian ocean can be modeled as a body of relatively pure water in equilibrium with a dense carbon dioxide atmosphere. The chemical weathering of lavas, pyroclastic deposits, and impact melt sheets would have the effect of neutralizing the acidity of the juvenile water. As calcium and other cations are added to the water by chemical weathering, they are quickly removed by the precipitation of calcium carbonate and other minerals, forming a deposit of limestone beneath the surface of the ocean. As the atmospheric carbon dioxide pressure and the temperature decrease, the Martian ocean would be completely frozen. Given the scenario for the chemical evolution of the northern lowland plains of Mars, it should be possible to draw a few conclusions about the expected mineralogy and geomorphology of this regions

Alligator Rivers Analogue project. Weathering and its effects on uranium redistribution

International Nuclear Information System (INIS)

Isobe, H.; Ohnuki, T.; Yanase, N.; Sato, T.; Kimura, H.; Sekine, K.; Nagano, T.; Klessa, D.A.; Conoley, C.; Nakashima, S.; Ewing, R.C.

1992-01-01

In the vicinity of the uranium ore deposit at Koongarra, quartz-chlorite schist, the ore host rock, has been subjected to weathering. Although quartz is resistant to weathering, chlorite has been altered to clays and iron minerals. The chlorite weathering and the uranium association with the weathered minerals are the main topics of this study. In order to clarify the weathering of chlorite and its effects on the redistribution of uranium, the processes, mechanisms, and kinetics of the chlorite weathering, and the uranium concentrations in minerals were examined by various methods: X-ray diffraction analysis, scanning electron microscopy, electron microprobe analysis, transmission electron microscopy, autoradiography, visible spectroscopy, alpha and gamma spectrometry. The observed results were compared to those calculated, based on two different models developed for the present study. Water-rock interactions have resulted in the weathering of chlorite and precipitation and sorption of uranyl from the groundwaters with the weathering products. It is concluded that the chlorite weathering affects the uranium retardation factor, and thus uranium redistribution at Koongarra. 55 refs., 20 tabs., 120 figs

Genetic interpretations of elemental and chemical differences in a soil chronosequence, California

Science.gov (United States)

Harden, J.W.

1988-01-01

Soils developed on fluvial terraces in central California have similar parent materials, climatic settings, vegetation cover and slopes but range in age from 40,000 to 3,000,000 years. The soils have chemical compositions that change systematically with increasing age. Such chemical differentiation is most likely the result of long-term weathering and mineralogical transformations that occurred since deposition of terrace fills and stabilization of the geomorphic surfaces. The changes in composition with time closely mimic other studies on mineral weathering, in which alkali and alkali-earth elements are lost more rapidly than transitional elements. The relative rates of element loss were determined by changes in element ratios over time. Net losses and gains of elements in different size fractions were monitored by their concentrations relative to Zr, the most stable constituent. Both sand and finer size fractions have lost considerable amounts of Ca, Mg, Na and K. Aluminum appears to have been lost from the sand fraction and gained in the fine fraction over a 3-million-year-time-span. Although there is no evidence for losses of Fe and Ti from sands, there is a net influx of Fe and Ti into finer fractions, probably gained from undetectable yet significant weathering of sand grains. Etching of sand grains, clay mineralogy, and microprobe analyses also indicate that the soils have undergone these chemical transformations during their formation. Mineralogical analyses also mimic other studies on mineral weathering, in which the pyroxenes weather more rapidly than hornblende, which weathers more rapidly than sphene or zircon. ?? 1988.

Geological and Chemical Factors that Impacted the Biological Utilization of Cobalt in the Archean Eon

Science.gov (United States)

Moore, Eli K.; Hao, Jihua; Prabhu, Anirudh; Zhong, Hao; Jelen, Ben I.; Meyer, Mike; Hazen, Robert M.; Falkowski, Paul G.

2018-03-01

The geosphere and biosphere coevolved and influenced Earth's biological and mineralogical diversity. Changing redox conditions influenced the availability of different transition metals, which are essential components in the active sites of oxidoreductases, proteins that catalyze electron transfer reactions across the tree of life. Despite its relatively low abundance in the environment, cobalt (Co) is a unique metal in biology due to its importance to a wide range of organisms as the metal center of vitamin B12 (aka cobalamin, Cbl). Cbl is vital to multiple methyltransferase enzymes involved in energetically favorable metabolic pathways. It is unclear how Co availability is linked to mineral evolution and weathering processes. Here we examine important biological functions of Co, as well as chemical and geological factors that may have influenced the utilization of Co early in the evolution of life. Only 66 natural minerals are known to contain Co as an essential element. However, Co is incorporated as a minor element in abundant rock-forming minerals, potentially representing a reliable source of Co as a trace element in marine systems due to weathering processes. We developed a mineral weathering model that indicates that dissolved Co was potentially more bioavailable in the Archean ocean under low S conditions than it is today. Mineral weathering, redox chemistry, Co complexation with nitrogen-containing organics, and hydrothermal environments were crucial in the incorporation of Co in primitive metabolic pathways. These chemical and geological characteristics of Co can inform the biological utilization of other trace metals in early forms of life.

Effect of Bacillus subtilis on Granite Weathering: A Laboratory Experiment

Science.gov (United States)

Song, W.; Ogawa, N.; Oguchi, C. T.; Hatta, T.; Matsukura, Y.

2006-12-01

We performed a comparative experiment to investigate how the ubiquitous soil bacterium Bacillus subtilis weathers granite and which granite-forming minerals weather more rapidly via biological processes. Batch type experiments (granite specimen in a 500 ml solution including NaCl, glucose, yeast extract and bacteria Bacillus subtilis at 27°E C) were carried out for 30 days. Granite surfaces were observed by SEM before and after the experiment. Bacillus subtilis had a strong influence on granite weathering by forming pits. There were 2.4 times as many pits and micropores were 2.3 times wider in granite exposed to Bacillus subtilis when compared with bacteria-free samples. Bacillus subtilis appear to preferentially select an optimum place to adhere to the mineral and dissolve essential elements from the mineral to live. Plagioclase was more vulnerable to bacterial weathering than biotite among the granite composing minerals.

Seismic Wave Propagation from Underground Chemical Explosions: Sensitivity to Velocity and Thickness of a Weathered Layer

Science.gov (United States)

Hirakawa, E. T.; Ezzedine, S. M.

2017-12-01

Recorded motions from underground chemical explosions are complicated by long duration seismic coda as well as motion in the tangential direction. The inability to distinguish the origins of these complexities as either source or path effects comprises a limitation to effective monitoring of underground chemical explosions. With numerical models, it is possible to conduct rigorous sensitivity analyses for chemical explosive sources and their resulting ground motions under the influence of many attributes, including but not limited to complex velocity structure, topography, and non-linear source characteristics. Previously we found that topography can cause significant scattering in the direct wave but leads to relatively little motion in the coda. Here, we aim to investigate the contribution from the low-velocity weathered layer that exists in the shallow subsurface apart from and in combination with surface topography. We use SW4, an anelastic anisotropic fourth order finite difference code to simulate chemical explosive source in a 1D velocity structure consisting of a single weathered layer over a half space. A range of velocity magnitudes are used for the upper weathered layer with the velocities always being lower than that of the granitic underlaying layer. We find that for lower weathered layer velocities, the wave train is highly dispersed and causes a large percentage of energy to be contained in the coda in relation to the entire time series. The percentage of energy contained in the coda grows with distance from the source but saturates at a certain distance that depends on weathered layer velocity and thickness. The saturation onset distance increases with decreasing layer thickness and increasing velocity of the upper layer. Measurements of relative coda energy and coda saturation onset distance from real recordings can provide an additional constraint on the properties of the weathered layer in remote sites as well as test sites like the Nevada

Carbon storage and nutrient mobilization from soil minerals by deep roots and rhizospheres

DEFF Research Database (Denmark)

Callesen, Ingeborg; Harrison, Robert; Stupak, Inge

2016-01-01

studies on potential release of nutrients due to chemical weathering indicate the importance of root access to deep soil layers. Nutrient release profiles clearly indicate depletion in the top layers and a much higher potential in B and C horizons. Reviewing potential sustainability of nutrient supplies......Roots mobilize nutrients via deep soil penetration and rhizosphere processes inducing weathering of primary minerals. These processes contribute to C transfer to soils and to tree nutrition. Assessments of these characteristics and processes of root systems are important for understanding long......-term supplies of nutrient elements essential for forest growth and resilience. Research and techniques have significantly advanced since Olof Tamm’s 1934 “base mineral index” for Swedish forest soils, and the basic nutrient budget estimates for whole-tree harvesting systems of the 1970s. Recent research...

Final Report: Caustic Waste-Soil Weathering Reactions and Their Impacts on Trace Contaminant Migration and Sequestration

International Nuclear Information System (INIS)

O'Day, Peggy A.; Chorover, J.; Mueller, K.T.; Serne, R.J.

2006-01-01

The principal goal of this project was to assess the molecular nature and stability of radionuclide (137-Cs, 90-Sr, and 129-I) immobilization during weathering reactions in bulk Hanford sediments and their high surface area clay mineral constituents. We focused on the unique aqueous geochemical conditions that are representative of waste-impacted locations in the Hanford site vadose zone: high ionic strength, high pH and high Al concentrations. The specific objectives of the work were to (i) measure the coupling of clay mineral weathering and contaminant uptake kinetics of Cs+, Sr2+ and I-; (ii) determine the molecular structure of contaminant binding sites and their change with weathering time during and after exposure to synthetic tank waste leachate (STWL); (iii) establish the stability of neoformed weathering products and their sequestered contaminants upon exposure of the solids to more ''natural'' soil solutions (i.e., after removal of the caustic waste source); and (iv) integrate macroscopic, microscopic and spectroscopic data to distinguish labile from non-labile contaminant binding environments, including their dependence on system composition and weathering time. During this funding period, we completed a large set of bench-scale collaborative experiments and product characterization aimed at elucidating the coupling between mineral transformation reactions and contaminant sequestration/stabilization. Our experiments included three representative Hanford sediments: course and fine sediments collected from the Hanford Formation and Ringold Silt, in addition to investigations with specimen clay minerals illite, vermiculite, smectite and kaolinite. These experiments combined macroscopic measurements of element release, contaminant uptake and subsequent neoformed mineral dissolution behavior, with detailed studies of solid phase products using SEM and TEM microscopy, NMR, XAS and FTIR spectroscopy. Our studies have shown direct coupling between mineral

Colluvial deposits as a possible weathering reservoir in uplifting mountains

Directory of Open Access Journals (Sweden)

S. Carretier

2018-03-01

Full Text Available The role of mountain uplift in the evolution of the global climate over geological times is controversial. At the heart of this debate is the capacity of rapid denudation to drive silicate weathering, which consumes CO2. Here we present the results of a 3-D model that couples erosion and weathering during mountain uplift, in which, for the first time, the weathered material is traced during its stochastic transport from the hillslopes to the mountain outlet. To explore the response of weathering fluxes to progressively cooler and drier climatic conditions, we run model simulations accounting for a decrease in temperature with or without modifications in the rainfall pattern based on a simple orographic model. At this stage, the model does not simulate the deep water circulation, the precipitation of secondary minerals, variations in the pH, below-ground pCO2, and the chemical affinity of the water in contact with minerals. Consequently, the predicted silicate weathering fluxes probably represent a maximum, although the predicted silicate weathering rates are within the range of silicate and total weathering rates estimated from field data. In all cases, the erosion rate increases during mountain uplift, which thins the regolith and produces a hump in the weathering rate evolution. This model thus predicts that the weathering outflux reaches a peak and then falls, consistent with predictions of previous 1-D models. By tracking the pathways of particles, the model can also consider how lateral river erosion drives mass wasting and the temporary storage of colluvial deposits on the valley sides. This reservoir is comprised of fresh material that has a residence time ranging from several years up to several thousand years. During this period, the weathering of colluvium appears to sustain the mountain weathering flux. The relative weathering contribution of colluvium depends on the area covered by regolith on the hillslopes. For mountains

Adsorption of Nucleic Acid Bases, Ribose, and Phosphate by Some Clay Minerals

Directory of Open Access Journals (Sweden)

Hideo Hashizume

2015-02-01

Full Text Available Besides having a large capacity for taking up organic molecules, clay minerals can catalyze a variety of organic reactions. Derived from rock weathering, clay minerals would have been abundant in the early Earth. As such, they might be expected to play a role in chemical evolution. The interactions of clay minerals with biopolymers, including RNA, have been the subject of many investigations. The behavior of RNA components at clay mineral surfaces needs to be assessed if we are to appreciate how clays might catalyze the formation of nucleosides, nucleotides and polynucleotides in the “RNA world”. The adsorption of purines, pyrimidines and nucleosides from aqueous solution to clay minerals is affected by suspension pH. With montmorillonite, adsorption is also influenced by the nature of the exchangeable cations. Here, we review the interactions of some clay minerals with RNA components.

Mobility of nutrients and trace metals during weathering in the late Archean

Science.gov (United States)

Hao, Jihua; Sverjensky, Dimitri A.; Hazen, Robert M.

2017-08-01

The evolution of the geosphere and biosphere depends on the availability of bio-essential nutrients and trace metals. Consequently, the chemical and isotopic variability of trace elements in the sedimentary record have been widely used to infer the existence of early life and fluctuations in the near-surface environment on the early Earth, particularly fluctuations in the redox state of the atmosphere. In this study, we applied late Archean weathering models (Hao et al., 2017), developed to estimate the behavior of major elements and the composition of late Archean world average river water, to explore the behavior of nutrient and trace metals and their potential for riverine transport. We focused on P, Mn, Cr, and Cu during the weathering of olivine basalt. In our standard late Archean weathering model (pCO2,g = 10-1.5 bars, pH2,g = 10-5.0 bars), crustal apatite was totally dissolved by the acidic rainwater during weathering. Our model quantitatively links the pCO2,g of the atmosphere to phosphate levels transported by rivers. The development of late Archean river water (pH = 6.4) resulted in riverine phosphate of at least 1.7 μmolar, much higher than at the present-day. At the end of the early Proterozoic snowball Earth event when pCO2,g could be 0.01-0.10 bars, river water may have transported up to 70 μmolar phosphate, depending on the availability of apatite, thereby stimulating high levels of oxygenic photosynthesis in the marine environment. Crustal levels of Mn in olivine dissolved completely during weathering, except at large extents of weathering where Mn was stored as a component of a secondary carbonate mineral. The corresponding Mn content of river water, about 1.2 μmolar, is higher than in modern river water. Whiffs of 10-5 mole O2 gas or HNO3 kg-1 H2O resulted in the formation of pyrolusite (MnO2) and abundant hematite and simultaneous dramatic decreases in the concentration of Mn(II) in the river water. Chromite dissolution resulted in negligible

Differential rates of feldspar weathering in granitic regoliths

Science.gov (United States)

White, A.F.; Bullen, T.D.; Schulz, M.S.; Blum, A.E.; Huntington, T.G.; Peters, N.E.

2001-01-01

Differential rates of plagioclase and K-feldspar weathering commonly observed in bedrock and soil environments are examined in terms of chemical kinetic and solubility controls and hydrologic permeability. For the Panola regolith, in the Georgia Piedmont Province of southeastern United States, petrographic observations, coupled with elemental balances and 87Sr/86Sr ratios, indicate that plagioclase is being converted to kaolinite at depths > 6 m in the granitic bedrock. K-feldspar remains pristine in the bedrock but subsequently weathers to kaolinite at the overlying saprolite. In contrast, both plagioclase and K-feldspar remain stable in granitic bedrocks elsewhere in Piedmont Province, such as Davis Run, Virginia, where feldspars weather concurrently in an overlying thick saprolite sequence. Kinetic rate constants, mineral surface areas, and secondary hydraulic conductivities are fitted to feldspar losses with depth in the Panola and Davis Run regoliths using a time-depth computer spreadsheet model. The primary hydraulic conductivities, describing the rates of meteoric water penetration into the pristine granites, are assumed to be equal to the propagation rates of weathering fronts, which, based on cosmogenic isotope dating, are 7 m/106 yr for the Panola regolith and 4 m/106 yr for the Davis Run regolith. Best fits in the calculations indicate that the kinetic rate constants for plagioclase in both regoliths are factors of two to three times faster than K-feldspar, which is in agreement with experimental findings. However, the range for plagioclase and K-feldspar rates (kr = 1.5 x 10-17 to 2.8 x 10-16 mol m-2 s-1) is three to four orders of magnitude lower than for that for experimental feldspar dissolution rates and are among the slowest yet recorded for natural feldspar weathering. Such slow rates are attributed to the relatively old geomorphic ages of the Panola and Davis Run regoliths, implying that mineral surface reactivity decreases significantly with

Thermodynamic Cconstraints on Coupled Carbonate-Pyrite Weathering Dynamics and Carbon Fluxes

Science.gov (United States)

Winnick, M.; Maher, K.

2017-12-01

Chemical weathering within the critical zone regulates global biogeochemical cycles, atmospheric composition, and the supply of key nutrients to terrestrial and aquatic ecosystems. Recent studies suggest that thermodynamic limits on solute production act as a first-order control on global chemical weathering rates; however, few studies have addressed the factors that set these thermodynamic limits in natural systems. In this presentation, we investigate the effects of soil CO2 concentrations and pyrite oxidation rates on carbonate dissolution and associated carbon fluxes in the East River watershed in Colorado, using concentration-discharge relationships and thermodynamic constraints. Within the shallow subsurface, soil respiration rates and moisture content determine the extent of carbonic acid-promoted carbonate dissolution through their modulation of soil pCO2 and the balance of open- v. closed-system weathering processes. At greater depths, pyrite oxidation generates sulfuric acid, which alters the approach to equilibrium of infiltrating waters. Through comparisons of concentration-discharge data and reactive transport model simulations, we explore the conditions that determine whether sulfuric acid reacts to dissolve additional carbonate mineral or instead reacts with alkalinity already in solution - the balance of which determines watershed carbon flux budgets. Our study highlights the importance of interactions between the chemical structure of the critical zone and the hydrologic regulation of flowpaths in determining concentration-discharge relationships and overall carbon fluxes.

Specificity of pyrometamorphic minerals of the ellestadite group

Science.gov (United States)

Zateeva, S. N.; Sokol, E. V.; Sharygin, V. V.

2007-12-01

Numerous rare and new mineral species are synthesized during the process of pyrometamorphism (Gross, 1977; Chesnokov et al., 1987; Chesnokov and Shcherbakova, 1991; Chesnokov, 1999), including silicooxides, chloride-, fluoride, and sulfate-silicates, carbonate-sulfides, chloride-oxides, etc. Having made sense of numerous findings of compounds of this type, Chesnokov (1999) set forth the concept of the crystallochemical transition at extreme temperatures attaining 1200-1450°C in pyrogenic systems. First of all, intertype transitions (oxygen-bearing-oxygen-free) and interclass transitions (chloride-silicate, carbonate-sulfide, chlorideoxide) are realized. The specificity of pyrometamorphic mineral assemblages consists in the abundance of silicates with additional anions (F-, Cl-, (CO3)2-) (Sokol et al., 2005). Minerals of the ellestadite group Ca10(SiO4)3 - x (SO4)3 - x (PO4)2 x (OH,F,Cl)2 are a spectacular example of these features. In the general case, they are silicate-sulfate-phosphate-hydroxide-chlorides-fluorides. The detailed description of these minerals based on the study of the original collection of pyrometamorphic minerals is presented in this paper.

Geochemical behavior under tropical weathering of the Barama-Mazaruni greenstone belt at Omai gold mine, Guiana Shield

Energy Technology Data Exchange (ETDEWEB)

Voicu, G. [Universite du Quebec a Montreal (Canada). Dept. des Sciences de la Terre et de l' Atmosphere; Omai Gold Mines, Georgetown (Guyana); Bardoux, M. [Universite du Quebec a Montreal (Canada). Dept. des Sciences de la Terre et de l' Atmosphere

2002-07-01

Mineralogical, petrographical, and geochemical studies of the weathering profile have been carried out at Omai Au mine, Guyana. The area is underlain by felsic to mafic volcanic and sedimentary rocks of the Barama-Mazaruni Supergroup, part of the Paleoproterozoic greenstone belts of the Guiana Shield. Tropical rainy climate has favoured extensive lateritization processes and formation of a deeply weathered regolith. The top of the weathering profile consists of lateritic gravel or is masked by the Pleistocene continental-deltaic Berbice Formation. Mineralogical composition of regolith consists mainly of kaolinite, goethite and quark, and subordinately sericite, feldspar, hematite, pyrite, smectite, heavy minerals, and uncommon mineral phases (nacrite, ephesite, corrensite, guyanaite). A specific feature of the weathering profile at Omai is the preservation of fresh hydrothermal pyrite in the saprolith horizon. Chemical changes during the weathering processes depend on various physicochemical and structural parameters. Consequently, the depth should not be the principal criterion for comparison purposes of the geochemical behavior within the weathering profile, but rather an index that measures the degree of supergene alteration that has affected each analyzed sample, independently of the depth of sampling. Thus, the mineralogical index of alteration (MIA) can provide more accurate information about the behavior of major and trace elements in regolith as opposed to unweathered bedrock. It can also aid in establishing a quantitative relationship between intensity of weathering and mobility (leaching or accumulation) of each element in each analyzed sample. At Omai, some major and trace elements that are commonly considered as immobile (ex: TiO{sub 2}, Zr, etc.) during weathering could become mobile in several rock types and cannot be used to calculate the mass and volume balance. In addition, due to higher ''immobile element'' ratios, the

Basis for paleoenvironmental interpretation of magnetic properties of sediment from Upper Klamath Lake (Oregon): Effects of weathering and mineralogical sorting

Science.gov (United States)

Rosenbaum, J.G.; Reynolds, R.L.

2004-01-01

Studies of magnetic properties enable reconstruction of environmental conditions that affected magnetic minerals incorporated in sediments from Upper Klamath Lake. Analyses of stream sediment samples from throughout the catchment of Upper Klamath Lake show that alteration of Fe-oxide minerals during subaerial chemical weathering of basic volcanic rocks has significantly changed magnetic properties of surficial deposits. Titanomagnetite, which is abundant both as phenocrysts and as microcrystals in fresh volcanic rocks, is progressively destroyed during weathering. Because fine-grained magnetite is readily altered due to large surface-to-volume ratios, weathering causes an increase in average magnetic grain size as well as reduction in the quantity of titanomagnetite both absolutely and relative to hematite. Hydrodynamic mineralogical sorting also produces differences in magnetic properties among rock and mineral grains of differing sizes. Importantly, removal of coarse silicate and Fe-oxide grains by sorting concentrated extremely fine-grained magnetite in the resulting sediment. The effects of weathering and sorting of minerals cannot be completely separated. These processes combine to produce the magnetic properties of a non-glacial lithic component of Upper Klamath Lake sediments, which is characterized by relatively low magnetite content and coarse magnetic grain size. Hydrodynamic sorting alone causes significant differences between the magnetic properties of glacial flour in lake sediments and of fresh volcanic rocks in the catchment. In comparison to source volcanic rocks, glacial flour in the lake sediment is highly enriched in extremely fine-grained magnetite.

Quantifying nutrient uptake as driver of rock weathering in forest ecosystems by magnesium stable isotopes

Directory of Open Access Journals (Sweden)

D. Uhlig

2017-06-01

Full Text Available Plants and soil microbiota play an active role in rock weathering and potentially couple weathering at depth with erosion at the soil surface. The nature of this coupling is still unresolved because we lacked means to quantify the passage of chemical elements from rock through higher plants. In a temperate forested landscape characterised by relatively fast (∼ 220 t km−2 yr−1 denudation and a kinetically limited weathering regime of the Southern Sierra Critical Zone Observatory (SSCZO, California, we measured magnesium (Mg stable isotopes that are sensitive indicators of Mg utilisation by biota. We find that Mg is highly bio-utilised: 50–100 % of the Mg released by chemical weathering is taken up by forest trees. To estimate the tree uptake of other bio-utilised elements (K, Ca, P and Si we compared the dissolved fluxes of these elements and Mg in rivers with their solubilisation fluxes from rock (rock dissolution flux minus secondary mineral formation flux. We find a deficit in the dissolved fluxes throughout, which we attribute to the nutrient uptake by forest trees. Therefore both the Mg isotopes and the flux comparison suggest that a substantial part of the major element weathering flux is consumed by the tree biomass. The enrichment of 26Mg over 24Mg in tree trunks relative to leaves suggests that tree trunks account for a substantial fraction of the net uptake of Mg. This isotopic and elemental compartment separation is prevented from obliteration (which would occur by Mg redissolution by two potential effects. Either the mineral nutrients accumulate today in regrowing forest biomass after clear cutting, or they are exported in litter and coarse woody debris (CWD such that they remain in solid biomass. Over pre-forest-management weathering timescales, this removal flux might have been in operation in the form of natural erosion of CWD. Regardless of the removal mechanism, our approach provides entirely novel means towards

Quantifying nutrient uptake as driver of rock weathering in forest ecosystems by magnesium stable isotopes

Science.gov (United States)

Uhlig, David; Schuessler, Jan A.; Bouchez, Julien; Dixon, Jean L.; von Blanckenburg, Friedhelm

2017-06-01

Plants and soil microbiota play an active role in rock weathering and potentially couple weathering at depth with erosion at the soil surface. The nature of this coupling is still unresolved because we lacked means to quantify the passage of chemical elements from rock through higher plants. In a temperate forested landscape characterised by relatively fast (˜ 220 t km-2 yr-1) denudation and a kinetically limited weathering regime of the Southern Sierra Critical Zone Observatory (SSCZO), California, we measured magnesium (Mg) stable isotopes that are sensitive indicators of Mg utilisation by biota. We find that Mg is highly bio-utilised: 50-100 % of the Mg released by chemical weathering is taken up by forest trees. To estimate the tree uptake of other bio-utilised elements (K, Ca, P and Si) we compared the dissolved fluxes of these elements and Mg in rivers with their solubilisation fluxes from rock (rock dissolution flux minus secondary mineral formation flux). We find a deficit in the dissolved fluxes throughout, which we attribute to the nutrient uptake by forest trees. Therefore both the Mg isotopes and the flux comparison suggest that a substantial part of the major element weathering flux is consumed by the tree biomass. The enrichment of 26Mg over 24Mg in tree trunks relative to leaves suggests that tree trunks account for a substantial fraction of the net uptake of Mg. This isotopic and elemental compartment separation is prevented from obliteration (which would occur by Mg redissolution) by two potential effects. Either the mineral nutrients accumulate today in regrowing forest biomass after clear cutting, or they are exported in litter and coarse woody debris (CWD) such that they remain in solid biomass. Over pre-forest-management weathering timescales, this removal flux might have been in operation in the form of natural erosion of CWD. Regardless of the removal mechanism, our approach provides entirely novel means towards the direct quantification of

Chemical Alteration of Soils on Earth as a Function of Precipitation: Insights Into Weathering Processes Relevant to Mars

Science.gov (United States)

Amundson, R.; Chadwick, O.; Ewing, S.; Sutter, B.; Owen, J.; McKay, C.

2004-12-01

Soils lie at the interface of the atmosphere and lithosphere, and the rates of chemical and physical processes that form them hinge on the availability of water. Here we quantify the effect of these processes on soil volume and mass in different rainfall regimes. We then use the results of this synthesis to compare with the growing chemical dataset for soils on Mars in order to identify moisture regimes on Earth that may provide crude analogues for past Martian weathering conditions. In this synthesis, the rates of elemental gains/losses, and corresponding volumetric changes, were compared for soils in nine soil chronosequences (sequences of soils of differing ages) - sequences formed in climates ranging from ~1 to ~4500 mm mean annual precipitation (MAP). Total elemental chemistry of soils and parent materials were determined via XRF, ICP-MS, and/or ICP-OES, and the absolute elemental gains or losses (and volume changes) were determined by normalizing data to an immobile index element. For the chronosequences examined, the initial stages of soil formation (103^ to 104^ yr), regardless of climate, generally show volumetric expansion due to (1) reduction in bulk density by biological/physical turbation, (2) addition of organic matter, (3) accumulation of water during clay mineral synthesis, and/or (4) accumulation of atmospheric salts and dust. Despite large differences in parent materials (basalt, sandstone, granitic alluvium), there was a systematic relationship between long-term (105^ to 106^ yr) volumetric change and rainfall, with an approximate cross-over point between net expansion (and accumulation of atmospheric solutes and dust) and net collapse (net losses of Si, Al, and alkaline earths and alkali metals) between approximately 20 and 100 mm MAP. Recently published geochemical data of soils at Gusev Crater (Gellert et al. 2004. Science 305:829), when normalized to Ti, show apparent net losses of Si and Al that range between 5 and 50% of values relative to

Beneath it all: bedrock geology of the Catskill Mountains and implications of its weathering.

Science.gov (United States)

Ver Straeten, Charles A

2013-09-01

The Devonian-age bedrock of the Catskill Mountains has been the focus of many studies. This paper reviews the character and composition of the rocks of the Catskills, and examines weathering (rock decay) processes and their implications in the Catskills. Rocks of the Catskills and closest foothills consist of siliciclastic rocks (sandstones, mudrocks, conglomerates) with minimal, locally dispersed carbonate rocks. The former are dominated by quartz, metamorphic and sedimentary rock fragments, and clay minerals. Other minor sediment components include cements, authigenic and heavy minerals, and fossil organic matter. Physical, chemical, and biological weathering of the Catskill bedrock since uplift of the Appalachian region, combined with glaciation, have dissected a plateau of nearly horizontally layered rocks into a series of ridges, valleys, and peaks. The varied weathering processes, in conjunction with many factors (natural and anthropogenic), fragment the rocks, forming sediment and releasing various elements and compounds. These may have positive, neutral, or negative implications for the region's soils, waters, ecology, and human usage. A new generation of studies and analyses of the Catskill bedrock is needed to help answer a broad set of questions and problems across various fields of interest. © 2013 New York Academy of Sciences.

Microbially mediated mineral carbonation

Science.gov (United States)

Power, I. M.; Wilson, S. A.; Dipple, G. M.; Southam, G.

2010-12-01

Mineral carbonation involves silicate dissolution and carbonate precipitation, which are both natural processes that microorganisms are able to mediate in near surface environments (Ferris et al., 1994; Eq. 1). (Ca,Mg)SiO3 + 2H2CO3 + H2O → (Ca,Mg)CO3 + H2O + H4SiO4 + O2 (1) Cyanobacteria are photoautotrophs with cell surface characteristics and metabolic processes involving inorganic carbon that can induce carbonate precipitation. This occurs partly by concentrating cations within their net-negative cell envelope and through the alkalinization of their microenvironment (Thompson & Ferris, 1990). Regions with mafic and ultramafic bedrock, such as near Atlin, British Columbia, Canada, represent the best potential sources of feedstocks for mineral carbonation. The hydromagnesite playas near Atlin are a natural biogeochemical model for the carbonation of magnesium silicate minerals (Power et al., 2009). Field-based studies at Atlin and corroborating laboratory experiments demonstrate the ability of a microbial consortium dominated by filamentous cyanobacteria to induce the precipitation of carbonate minerals. Phototrophic microbes, such as cyanobacteria, have been proposed as a means for producing biodiesel and other value added products because of their efficiency as solar collectors and low requirement for valuable, cultivable land in comparison to crops (Dismukes et al., 2008). Carbonate precipitation and biomass production could be facilitated using specifically designed ponds to collect waters rich in dissolved cations (e.g., Mg2+ and Ca2+), which would allow for evapoconcentration and provide an appropriate environment for growth of cyanobacteria. Microbially mediated carbonate precipitation does not require large quantities of energy or chemicals needed for industrial systems that have been proposed for rapid carbon capture and storage via mineral carbonation (e.g., Lackner et al., 1995). Therefore, this biogeochemical approach may represent a readily

Weathering of Roofing Materials-An Overview

Energy Technology Data Exchange (ETDEWEB)

Berdahl, Paul; Akbari, Hashem; Levinson, Ronnen; Miller, William A.

2006-03-30

An overview of several aspects of the weathering of roofing materials is presented. Degradation of materials initiated by ultraviolet radiation is discussed for plastics used in roofing, as well as wood and asphalt. Elevated temperatures accelerate many deleterious chemical reactions and hasten diffusion of material components. Effects of moisture include decay of wood, acceleration of corrosion of metals, staining of clay, and freeze-thaw damage. Soiling of roofing materials causes objectionable stains and reduces the solar reflectance of reflective materials. (Soiling of non-reflective materials can also increase solar reflectance.) Soiling can be attributed to biological growth (e.g., cyanobacteria, fungi, algae), deposits of organic and mineral particles, and to the accumulation of flyash, hydrocarbons and soot from combustion.

Rare earth minerals and resources in the world

Energy Technology Data Exchange (ETDEWEB)

Kanazawa, Yasuo [Human Resource Department, National Institute of Advanced Industrial Science and Technology (AIST), 1-1-1 Umezono, Tsukuba 305-8568 (Japan)]. E-mail: y.kanazawa@aist.go.jp; Kamitani, Masaharu [Institute for Geo-Resources and Environment, National Institute of Advanced Industrial Science and Technology (AIST), 1-1-1 Higashi, Tsukuba 305-8567 (Japan)

2006-02-09

About 200 rare earth (RE) minerals are distributed in a wide variety of mineral classes, such as halides, carbonates, oxides, phosphates, silicates, etc. Due to the large ionic radii and trivalent oxidation state, RE ions in the minerals have large coordination numbers (c.n.) 6-10 by anions (O, F, OH). Light rare earth elements (LREEs) tend to occupy the larger sites of 8-10 c.n. and concentrate in carbonates and phosphates. On the other hand, heavy rare earth elements (HREEs) and Y occupy 6-8 c.n. sites and are abundant in oxides and a part of phosphates. Only a few mineral species, such as bastnaesite (Ce,La)(CO{sub 3})F, monazite (Ce,La)PO{sub 4}, xenotime YPO{sub 4}, and RE-bearing clay have been recovered for commercial production. Bayan Obo, China is the biggest RE deposit in the world. One of probable hypotheses for ore geneses is that the deposit might be formed by hydrothermal replacement of carbonate rocks of sedimentary origin. The hydrothermal fluid may be derived from an alkaline-carbonatite intrusive series. Following Bayan Obo, more than 550 carbonatite/alkaline complex rocks constitute the majority of the world RE resources. The distribution is restricted to interior and marginal regions of continents, especially Precambrian cratons and shields, or related to large-scale rift structures. Main concentrated areas of the complexes are East African rift zones, northern Scandinavia-Kola peninsula, eastern Canada and southern Brazil. Representative sedimentary deposits of REE are placer- and conglomerate-types. The major potential countries are Australia, India, Brazil, and Malaysia. Weathered residual deposits have been formed under tropical and sub-tropical climates. Bauxite and laterite nickel deposit are the representative. Ion adsorption clay without radioactive elements is known in southern China. Weathering processes concentrate REE in a particular clay mineral-layer in the weathered crusts whose source were originally REE-rich rocks like granite

Rare earth minerals and resources in the world

International Nuclear Information System (INIS)

Kanazawa, Yasuo; Kamitani, Masaharu

2006-01-01

About 200 rare earth (RE) minerals are distributed in a wide variety of mineral classes, such as halides, carbonates, oxides, phosphates, silicates, etc. Due to the large ionic radii and trivalent oxidation state, RE ions in the minerals have large coordination numbers (c.n.) 6-10 by anions (O, F, OH). Light rare earth elements (LREEs) tend to occupy the larger sites of 8-10 c.n. and concentrate in carbonates and phosphates. On the other hand, heavy rare earth elements (HREEs) and Y occupy 6-8 c.n. sites and are abundant in oxides and a part of phosphates. Only a few mineral species, such as bastnaesite (Ce,La)(CO 3 )F, monazite (Ce,La)PO 4 , xenotime YPO 4 , and RE-bearing clay have been recovered for commercial production. Bayan Obo, China is the biggest RE deposit in the world. One of probable hypotheses for ore geneses is that the deposit might be formed by hydrothermal replacement of carbonate rocks of sedimentary origin. The hydrothermal fluid may be derived from an alkaline-carbonatite intrusive series. Following Bayan Obo, more than 550 carbonatite/alkaline complex rocks constitute the majority of the world RE resources. The distribution is restricted to interior and marginal regions of continents, especially Precambrian cratons and shields, or related to large-scale rift structures. Main concentrated areas of the complexes are East African rift zones, northern Scandinavia-Kola peninsula, eastern Canada and southern Brazil. Representative sedimentary deposits of REE are placer- and conglomerate-types. The major potential countries are Australia, India, Brazil, and Malaysia. Weathered residual deposits have been formed under tropical and sub-tropical climates. Bauxite and laterite nickel deposit are the representative. Ion adsorption clay without radioactive elements is known in southern China. Weathering processes concentrate REE in a particular clay mineral-layer in the weathered crusts whose source were originally REE-rich rocks like granite and

Specific weather biotrop factors in the mountain resorts of North Caucasus

Science.gov (United States)

Efimenko, Natalia; Chalaya, Elena; Povolotckaia, Nina; Senik, Irina; Slepykh, Victor

2015-04-01

Key aspects of weather therapeutic action in the mountain resorts of the Northern Caucasus (RNC) are formed under the combined influence of global, regional and local atmospheric processes, picturesque landscape, vegetation which create specificity and attraction of the weather regime for the interests of resort rehabilitation, recreation and tourism practically during the whole year. They include high purity of surface atmosphere (background level of aerosols for the countryside, the transparency of the atmosphere 0.780 -0.890); natural hypo barium and hypoxia (5-10%); increased natural aeroionization (N+=400-1000 ion/cm3; N- = 600-1200 ion/cm3; KUI = 0.8 -1.0); the softness of temperature rate (± 600 W/m ); regime of solar radiation favourable for heliotherapy. Pathogenic effects in the mountains can occur both in front atmospheric processes and in conditions of relatively favorable weather. For example, in a stable anti-cyclonic air mass with the sunny weather, foehn effects can happen that are accompanied by excessively low air humidity (lower than 20-30%), the air temperature rises in the afternoon (in winter until 15- 20°C, in summer - up to 25-35°C). The situation can be worsened by ozone intrusion (O3) with the increase of its concentration by 20 ppb or more, temperature stratification change, formation of pollution accumulation conditions in the gorges and valleys where the resort towns are located. We can observe: the increase in the concentration of aerosol pollution from 1.78 to 4 and even up to 8-10 particles/cm (particle diameter is 500-1000 nm); the rise in mass concentration of submicron aerosol up to 75 mkg/m3 and the gas pollution (CO, COx, O3) of the surface atmosphere. Against this backdrop the effects of rapid changes in the chemical composition of natural ions due to the formation of positive nitrogen ions (often with a prevalence of positive over negative air ions) can be sometimes developed. In such situations people suffering from

Geochemical Weathering in Glacial and Proglacial Environments

Science.gov (United States)

Tranter, M.

2003-12-01

It seems counterintuitive that chemical erosion in glaciated regions proceeds at rates comparable to those of temperate catchments with comparable specific runoff (Anderson et al., 1997). All the usual factors that are associated with elevated rates of chemical weathering ( Drever, 1988, 1994), such as water, soil, and vegetation, are either entirely absent or absent for much of the year. For example, glaciated regions are largely frozen for significant periods each year, the residence time of liquid water in the catchment is low ( Knight, 1999), there are thin, skeletal soils at best, and vegetation is either absent or limited ( French, 1997). Other chapters in this volume have highlighted how these factors are important in other, more temperate and tropical environments. Even so, chemical erosion rates in glaciated terrain are usually near to or greater than the continental average ( Sharp et al., 1995; Wadham et al., 1997; Hodson et al., 2000). This is because glaciated catchments usually have high specific runoff, there are high concentrations of freshly comminuted rock flour, which is typically silt sized and coated with microparticles, and adsorbed organic matter or surface precipitates that may hinder water-rock interactions are largely absent ( Tranter, 1982). In short, the rapid flow of water over fine-grained, recently crushed, reactive mineral surfaces maximizes both the potential rates of chemical weathering and chemical erosion.A range of both lab- and field-based studies of glacial chemical weathering have been undertaken, mainly on the smaller glaciers of Continental Europe (e.g., Brown et al., 1993a, b), Svalbard (e.g., Hodson et al., 2002), and North America (e.g., Anderson et al., 2000). The field-based studies typically generate hydrographs of glacier runoff, which show a characteristic diurnal cycle during summer in low latitudes ( Figure 1), and more subdued diurnal cycles at high latitudes (Figure 2 and Figure 3). The concentration of ions in

Non-autoclaved aerated concrete with mineral additives

Science.gov (United States)

Il'ina, L. V.; Rakov, M. A.

2016-01-01

We investigated the effect of joint grinding of Portland cement clinker, silica and carbonate components and mineral additives to specific surface of 280 - 300 m2/kg on the properties (strength, average density and thermal conductivity) of non-autoclaved aerated concrete, and the porosity of the hardened cement paste produced from Portland cement clinker with mineral additives. The joint grinding of the Portland cement clinker with silica and carbonate components and mineral additives reduces the energy consumption of non-autoclaved aerated concrete production. The efficiency of mineral additives (diopside, wollastonite) is due to the closeness the composition, the type of chemical bonds, physical and chemical characteristics (specific enthalpy of formation, specific entropy) to anhydrous clinker minerals and their hydration products. Considering the influence of these additions on hydration of clinker minerals and formation of hardened cement paste structure, dispersed wollastonite and diopside should be used as mineral additives. The hardness and, consequently, the elastic modulus of diopside are higher than that of hardened cement paste. As a result, there is a redistribution of stresses in the hardened cement paste interporous partitions and hardening, both the partitions and aerated concrete on the whole. The mineral additives introduction allowed to obtain the non-autoclaved aerated concrete with average density 580 kg/m3, compressive strength of 3.3 MPa and thermal conductivity of 0.131 W/(m.°C).

Chemical composition and mineral elements of edible insects (at ...

African Journals Online (AJOL)

The Chemical Composition and Mineral Elements of two edible insects' larvae and termite soldiers were assayed. Their ash content were between 1.01% and 7.50%. The legless larva (LS) had 28.52% fat, while the solider ant had 7.14% and the Legged larva (LG) had 1.50%. The white ant (SA) had 15.61% protein while ...

Multifaceted role of clay minerals in pharmaceuticals

OpenAIRE

Khurana, Inderpreet Singh; Kaur, Satvinder; Kaur, Harpreet; Khurana, Rajneet Kaur

2015-01-01

The desirable physical and physiochemical properties of clay minerals have led them to play a substantial role in pharmaceutical formulations. Clay minerals like kaolin, smectite and palygorskite-sepiolite are among the world's most valuable industrial minerals and of considerable importance. The elemental features of clay minerals which caused them to be used in pharmaceutical formulations are high specific area, sorption capacity, favorable rheological properties, chemical inertness, swelli...

The correlation between selenium adsorption and the mineral and chemical composition of Taiwan local granite samples

Energy Technology Data Exchange (ETDEWEB)

Wang, TsingHai; Chiang, Chu-Ling; Wang, Chu-Fang [National Tsing Hua Univ., Hsinchu, Taiwan (China). Biomedical Engineering and Environmental Sciences

2015-07-01

Selenium-79 (Se-79) is a radioactive isotope of selenium, which is considered as one of the highly mobile nuclides since Se-79 would be presented in an anion species when dissolving into the intruded groundwater. Being an anionic species, the transport of Se-79 would be regulated by the metal oxides relevant minerals such as goethite and hematite (Jan et al., 2008). This is true that the transport of selenium in the shallow surface environment could be relatively easy to estimate by considering the amount of these metal oxides presenting in the soils and sediments. However, when dealing with deep geological repository, the transport of Se-79 becomes less predictable because of the much less content of metal oxide residing in the host rock such as granite. In order to conduct a reliable performance assessment of repository, it is very important to establish the correlation between selenium adsorption and the properties of potential host rock, in this study, the mineral and chemical compositions of Taiwan local granite. From this point of view, selenium adsorption experiments were conducted with 54 different Taiwan local granite samples collected from the depth ranging from 100 ∝ 400 meters below the surface. These granite samples represent a variety of deep geological environments, including the intact rock, groundwater intruded zones, and some weathered samples. Based upon our preliminary results, several solid conclusions could be made. First, the correlation coefficients between the Kd values and the mineral and chemical compositions are rather low (R-square values are often < 0.2). This points out the complexity of these geological samples and strongly suggests more efforts should be put into to acquire more relevant information. Second, the correlation between the selenium Kd values and the content of iron oxide (R-square 0.110) is much higher than that between the CEC of these granite samples (R-square 0.001). This clearly indicates that the minerals that

Weathering behavior of mine tailings and waste rock: A surface investigation

International Nuclear Information System (INIS)

Domvile, S.J.; Li, M.G.; Sollner, D.D.; Nesbitt, W.

1994-01-01

A study focusing on the ion movement in the near surface of sulfide minerals was conducted to better understand the weathering mechanisms of mine waste materials. Tailings and waste rock samples from Canadian mines were subjected to controlled weathering studies using various chemical leachants. Leachates were analyzed for various parameters, and petrographic analyses were conducted on the solid residues. Laboratory oxidation studies of pure pyrrhotite and arsenopyrite were carried out using the surface techniques X-ray photoelectron spectroscopy (XPS) and auger electron spectroscopy (AES). The data derived from the weathering study and the surface techniques were correlated to determine mechanisms of oxidation. Several results were observed during the project: ferric iron constitutes one third of the iron present in pyrrhotite, sulfide oxidation is initiated when rock is blasted, sulfide sulfur is oxidized to di- and poly-sulfides prior to forming sulfates, and significantly more sulfate is produced upon exposure to aqueous environments than to air alone

Testing the Control of Mineral Supply Rates on Chemical Erosion Rates in the Klamath Mountains

Science.gov (United States)

West, N.; Ferrier, K.

2016-12-01

The relationship between rates of chemical erosion and mineral supply is central to many problems in Earth science, including how tightly Earth's climate should be coupled to tectonics, how strongly nutrient supply to soils and streams depends on soil production, and how much lithology affects landscape evolution. Despite widespread interest in this relationship, there remains no consensus on how closely coupled chemical erosion rates should be to mineral supply rates. To address this, we have established a network of field sites in the Klamath Mountains along a latitudinal transect that spans an expected gradient in mineral supply rates associated with the geodynamic response to the migration of the Mendocino Triple Junction. Here, we present new measurements of regolith geochemistry and topographic analyses that will be compared with cosmogenic 10Be measurements to test hypotheses about supply-limited and kinetically-limited chemical erosion on granodioritic ridgetops. Previous studies in this area suggest a balance between rock uplift rates and basin wide erosion rates, implying the study ridgetops may have adjusted to an approximate steady state. Preliminary data are consistent with a decrease in chemical depletion fraction (CDF) with increasing ridgetop curvature. To the extent that ridgetop curvature reflects ridgetop erosion rates, this implies that chemical erosion rates at these sites are influenced by both mineral supply rates and dissolution kinetics.

Spatial gradient of chemical weathering and its coupling with physical erosion in the soils of the Betic Cordillera (SE Spain)

Science.gov (United States)

Schoonejans, Jerome; Vanacker, Veerle; Opfergelt, Sophie; Ameijeiras-Mariño, Yolanda; Kubik, Peter

2015-04-01

The production and denudation of soil material are controlled by chemical weathering and physical erosion which influence one another. Better understanding and quantification of this relationship is critical to understand biogeochemical cycles in the critical zone. The intense silicate weathering that is taking place in young mountain ranges is often cited to be a negative feedback that involves a long-term reduction of the atmospheric CO2 and the temperature cooling. However the possible (de)coupling between weathering and erosion is not fully understood for the moment and could reduce the effect of the feedback. This study is conducted in the eastern Betic Cordillera located in southeast Spain. The Betic Cordillera is composed by several mountains ranges or so-called Sierras that are oriented E-W to SE-NW and rise to 2000m.a.s.l. The Sierras differ in topographic setting, tectonic activity, and slightly in climate and vegetation. The mountain ranges located in the northwest, such as the Sierra Estancias, have the lowest uplift rates ( ~20-30 mm/kyr); while those in the southeast, such as the Sierra Cabrera, have the highest uplift rates ( >150mm/kyr). The sampling was realised into four small catchments located in three different Sierras. In each of them, two to three soil profiles were excavated on exposed ridgetops, and samples were taken by depth slices. The long-term denudation rate at the sites is inferred from in-situ 10Be CRN measurements. The chemical weathering intensity is constrained using a mass balance approach that is based on the concentration of immobile elements throughout the soil profile (CDF). Our results show that the soil depth decreases with an increase of the denudation rates. Chemical weathering accounts for 5 to 35% of the total mass lost due to denudation. Higher chemical weathering intensities (CDFs) are observed in sites with lower denudation rates (and vice versa). The data suggest that chemical weathering intensities are strongly

Paleo and present-day chemical weathering in lacustrine and riverine sediments in Northern Patagonia, Argentina

Energy Technology Data Exchange (ETDEWEB)

Roman Ross, Gabriela [Comision Nacional de Energia Atomica, San Carlos de Bariloche (Argentina). Centro Atomico Bariloche. Lab. de Analisis por Activacion Neutronica; Arribere, Maria A.; Guevara, Sergio Ribeiro [Universidad Nacional de Cuyo, XX (Argentina)

1996-07-01

Neutron activation analysis was used to study the abundance, distribution and fraction of REE (Rare Earth Elements) and diagnostic elements (Th, Co, Cr, Sc, Rb, Sr) in sediments from Mascardi lake and Upper Manso river. The local weathering patterns of this watershed show a strong influence of volcanic rocks with a selective mobilization of the more soluble elements. These patterns are very similar to those observed in a sedimentary lacustrine core from Mascardi lake. Paleolimnological record indicates a change in local fluxes of water and sediments, and an increase in organic matter content since the last full-glacial maximum. However, the chemical composition of the sedimentary inputs has not changed significantly during the last 14000 years. Our data support the hypothesis that present-day and Holocene chemical weathering have similar characteristics. All of the above conclusions are based on geochemical parameters only. (author)

Paleo and present-day chemical weathering in lacustrine and riverine sediments in Northern Patagonia, Argentina

International Nuclear Information System (INIS)

Roman Ross, Gabriela

1996-01-01

Neutron activation analysis was used to study the abundance, distribution and fraction of REE (Rare Earth Elements) and diagnostic elements (Th, Co, Cr, Sc, Rb, Sr) in sediments from Mascardi lake and Upper Manso river. The local weathering patterns of this watershed show a strong influence of volcanic rocks with a selective mobilization of the more soluble elements. These patterns are very similar to those observed in a sedimentary lacustrine core from Mascardi lake. Paleolimnological record indicates a change in local fluxes of water and sediments, and an increase in organic matter content since the last full-glacial maximum. However, the chemical composition of the sedimentary inputs has not changed significantly during the last 14000 years. Our data support the hypothesis that present-day and Holocene chemical weathering have similar characteristics. All of the above conclusions are based on geochemical parameters only. (author)

A literature survey of mineral-specific sorption data on radionuclides with relevance to the disposal of radioactive waste

International Nuclear Information System (INIS)

Delakowitz, B.; Meinrath, G.; Spiegel, W.

1996-01-01

A comparative review of mineral-specific radionuclide sorption databases created for performance assessment and reported in both the open literature and 'grey literature' (e.g. technical reports) has in part shown poor quality of documentation describing the database selection procedures. Inadequate information is available on the chemical species of the radionuclide under consideration and the laboratory conditions for determining K d -values. Sorption data derived from literature are neither comparable nor generally applicable due to the wide range in the composition of the aqueous and the solid phase applied in migration experiments. Subsequently, standardized characterization and determination procedures are needed. To improve the reliability of a mathematical model for the prediction of radionuclide sorption on cementitious and ash-type binder materials, determination of mineral-specific sorption coefficients is indispensable. (author). 31 refs., 1 fig., 2 tabs

Mineral and inorganic chemical composition of the Pernik coal, Bulgaria

Energy Technology Data Exchange (ETDEWEB)

Yossifova, Mariana G. [Geological Institute, Acad. G. Bonchev Str., Bl.24, Bulgarian Academy of Sciences, 1113 Sofia (Bulgaria)

2007-11-22

The mineral and inorganic chemical composition of five types of samples from the Pernik subbituminous coals and their products generated from the Pernik preparation plant were studied. They include feed coal, low-grade coal, high-grade coal, coal slime, and host rock. The mineral matter of the coals contains 44 species that belong mainly to silicates, carbonates, sulphates, sulphides, and oxides/hydroxides, and to a lesser extent, chlorides, biogenic minerals, and organic minerals. The detrital minerals are quartz, kaolinite, micas, feldspars, magnetite, cristobalite, spessartine, and amphibole. The authigenic minerals include various sulphides, silicates, oxihydroxides, sulphates, and carbonates. Several stages and substages of formation were identified during the syngenetic and epigenetic mineral precipitations of these coals. The authigenic minerals show the greatest diversity of mineral species as the epigenetic mineralization (mostly sulphides, carbonates, and sulphates) dominates qualitatively and quantitatively. The epigenetic mineralization was a result of complex processes occurring mostly during the late development of the Pernik basin. These processes indicate intensive tectonic, hydrothermal and volcanic activities accompanied by a change from fresh to marine sedimentation environment. Thermally altered organic matter due to some of the above processes was also identified in the basin. Most of the trace elements in the Pernik coals (Mo, Be, S, Zr, Y, Cl, Ba, Sc, Ga, Ag, V, P, Br, Ni, Co, Pb, Ca, and Ti) show an affinity to OM and phases intimately associated with OM. Some of the trace elements (Sr, Ti, Mn, Ba, Pb, Cu, Zn, Co, Cr, Ni, As, Ag, Yb, Sn, Ga, Ge, etc.) are impurities in authigenic and accessory minerals, while other trace elements (La, Ba, Cu, Ce, Sb, Bi, Zn, Pb, Cd, Nd, etc.) occur as discrete phases. Elements such as Sc, Be, Y, Ba, V, Zr, S, Mo, Ti, and Ga exceed Clarke concentrations in all of the coal types studied. It was also found that

Chemical and morphological characteristics of mineral trioxide aggregate and Portland cements.

Science.gov (United States)

Khan, Shahbaz; Kaleem, Muhammad; Fareed, Muhammad Amber; Habib, Amir; Iqbal, Kefi; Aslam, Ayesha; Ud Din, Shahab

2016-01-01

The purpose of this study was to investigate the chemical composition and particle morphology of white mineral trioxide aggregate (WMTA) and two white Portland cements (CEM 1 and CEM 2). Compositional analysis was performed by energy dispersive X-ray spectroscopy, X-ray fluorescence spectrometry and X-ray diffraction whereas, morphological characteristics were analyzed by scanning electron microscope and Laser scattering particle size distribution analyzer. The elemental composition of WMTA, CEM 1 and CEM 2 were similar except for the presence of higher amounts of bismuth in WMTA. Calcium oxide and silicon oxide constitute the major portion of the three materials whereas, tricalcium silicate was detected as the major mineral phase. The particle size distribution and morphology of WMTA was finer compared to CEM 1 and CEM 2. The three tested materials had relatively similar chemical composition and irregular particle morphologies.

Weathering of post-impact hydrothermal deposits from the Haughton impact structure: implications for microbial colonization and biosignature preservation.

Science.gov (United States)

Izawa, M R M; Banerjee, Neil R; Osinski, G R; Flemming, R L; Parnell, J; Cockell, C S

2011-01-01

active hydrothermal circulation produced primary mineral assemblages, including Fe sulfides, and was succeeded by a period dominated by oxidation and low-temperature hydration of primary minerals by surface waters. Active hydrothermal circulation can enable the rapid delivery of nutrients to microbes. Nutrient availability following the cessation of hydrothermal circulation is likely more restricted; therefore, the biological importance of chemical energy from hydrothermal mineral deposits increases with time. Weathering of primary hydrothermal deposits and dissolution and reprecipitation of mobile weathering products also create many potential habitats for endolithic microbes. They also provide a mechanism that may preserve biological materials, potentially over geological timescales. © Mary Ann Liebert, Inc.

The main chemical properties of hot and cold mineral waters in Bayankhongor, Mongolia

Directory of Open Access Journals (Sweden)

D Oyuntsetseg

2014-12-01

Full Text Available In the current study, hot and cold mineral springs and sub mineral waters in the Bayankhongor province were examined for their chemical characteristics and identified cold mineral waters classification according to mineral water classification of Mongolia. The hot spring waters belong to Na+-HCO3- and Na+-SO42- types. The cold mineral spring of Lkham belongs to Ca2+-HCO3- type. All sub mineral waters are generally located in the two areas (northern part or mountain forest area and the southern part or Gobi desert area. TDS concentrations of cold springs of the southern part in the study area were higher than northern part’s cold springs. The total dissolved silica content of cold spring was ranged from 4.5mg/L to 26 mg/L which did not correspond to requirements of mineral water standard of Mongolia. Thus, these cold springs are belonging to sub mineral water classification. The sub mineral waters were characterized into four types such as a Ca2+-SO42-, Na+-SO42-, Na+-HCO3 and Ca2+ - HCO3 by their chemical composition in the study area. The values for the quartz, chalcedony geothermometer and the Na/K geothermometer were quite different. The silica-enthalpy mixing model predicts a subsurface reservoir temperature between 124 and 197°C and most of the hot waters have been  probably mixed with cold water. The result shows that an averaged value of calculated temperature ranges from 77°C to 119°C which indicates that studied area has low temperature geothermal resources. DOI: http://doi.dx.org/10.5564/mjc.v15i0.324 Mongolian Journal of Chemistry 15 (41, 2014, p56-62

ANALYSES OF ROCK SURFACE COLOUR CHANGES DUE TO WEATHERING

OpenAIRE

GOKAY, Mehmet Kemal

2018-01-01

Description parameters of rock masses and minerals include their colours as well. Colours appear in daylight for surfaced rock masses are changing slightly due to weathering layers which have been covering its surface gradually. Healthy human eyes can manage to differentiate visible light spectrum to identify colours of substances including rock masses. Then visible blackish colours of magnetite minerals, reddish colours of Terra- Rosa soils, greenish colours of weathered copper ore, pure whi...

ANALYSES OF ROCK SURFACE COLOUR CHANGES DUE TO WEATHERING

OpenAIRE

GÖKAY, Mehmet Kemal

2018-01-01

Description parameters of rock masses and minerals include their colours as well. Colours appear in daylight for surfaced rock masses are changing slightly due to weathering layers which have been covering its surface gradually. Healthy human eyes can manage to differentiate visible spectrum to identify the colours of substance including rock masses. Then visible blackish colours of magnetite minerals, reddish colours of Terra- Rosa soils, greenish colours of weathered copper ore, pure white ...

Potential and costs of carbon dioxide removal by enhanced weathering of rocks

Science.gov (United States)

Strefler, Jessica; Amann, Thorben; Bauer, Nico; Kriegler, Elmar; Hartmann, Jens

2018-03-01

The chemical weathering of rocks currently absorbs about 1.1 Gt CO2 a-1 being mainly stored as bicarbonate in the ocean. An enhancement of this slow natural process could remove substantial amounts of CO2 from the atmosphere, aiming to offset some unavoidable anthropogenic emissions in order to comply with the Paris Agreement, while at the same time it may decrease ocean acidification. We provide the first comprehensive assessment of economic costs, energy requirements, technical parameterization, and global and regional carbon removal potential. The crucial parameters defining this potential are the grain size and weathering rates. The main uncertainties about the potential relate to weathering rates and rock mass that can be integrated into the soil. The discussed results do not specifically address the enhancement of weathering through microbial processes, feedback of geogenic nutrient release, and bioturbation. We do not only assess dunite rock, predominantly bearing olivine (in the form of forsterite) as the mineral that has been previously proposed to be best suited for carbon removal, but focus also on basaltic rock to minimize potential negative side effects. Our results show that enhanced weathering is an option for carbon dioxide removal that could be competitive already at 60 US  t-1 CO2 removed for dunite, but only at 200 US  t-1 CO2 removed for basalt. The potential carbon removal on cropland areas could be as large as 95 Gt CO2 a-1 for dunite and 4.9 Gt CO2 a-1 for basalt. The best suited locations are warm and humid areas, particularly in India, Brazil, South-East Asia and China, where almost 75% of the global potential can be realized. This work presents a techno-economic assessment framework, which also allows for the incorporation of further processes.

Advances in chemical and physical properties of electric arc furnace carbon steel slag by hot stage processing and mineral mixing.

Science.gov (United States)

Liapis, Ioannis; Papayianni, Ioanna

2015-01-01

Slags are recognised as a highly efficient, cost effective tool in the metal processing industry, by minimising heat losses, reducing metal oxidation through contact with air, removing metal impurities and protecting refractories and graphite electrodes. When compared to natural aggregates for use in the construction industry, slags have higher specific weight that acts as an economic deterrent. A method of altering the specific weight of EAFC slag by hot stage processing and mineral mixing, during steel production is presented in this article. The method has minimal interference with the production process of steel, even by limited additions of appropriate minerals at high temperatures. Five minerals are examined, namely perlite, ladle furnace slag, bauxite, diatomite and olivine. Measurements of specific weight are accompanied by X-ray diffraction (XRD) and fluorescence (XRF) analysis and scanning electron microscopy spectral images. It is also shown how altering the chemical composition is expected to affect the furnace refractory lining. Additionally, the process has been repeated for the most suitable mix in gas furnace and physical properties (FI, SI, LA, PSV, AAV, volume stability) examined. Alteration of the specific weight can result in tailoring slag properties for specific applications in the construction sector. Copyright © 2014 Elsevier B.V. All rights reserved.

Modeling Silicate Weathering for Elevated CO2 and Temperature

Science.gov (United States)

Bolton, E. W.

2016-12-01

A reactive transport model (RTM) is used to assess CO2 drawdown by silicate weathering over a wide range of temperature, pCO2, and infiltration rates for basalts and granites. Although RTM's have been used extensively to model weathering of basalts and granites for present-day conditions, we extend such modeling to higher CO2 that could have existed during the Archean and Proterozoic. We also consider a wide range of surface temperatures and infiltration rates. We consider several model basalt and granite compositions. We normally impose CO2 in equilibrium with the various atmospheric ranges modeled and CO2 is delivered to the weathering zone by aqueous transport. We also consider models with fixed CO2 (aq) throughout the weathering zone as could occur in soils with partial water saturation or with plant respiration, which can strongly influence pH and mineral dissolution rates. For the modeling, we use Kinflow: a model developed at Yale that includes mineral dissolution and precipitation under kinetic control, aqueous speciation, surface erosion, dynamic porosity, permeability, and mineral surface areas via sub-grid-scale grain models, and exchange of volatiles at the surface. Most of the modeling is done in 1D, but some comparisons to 2D domains with heterogeneous permeability are made. We find that when CO2 is fixed only at the surface, the pH tends toward higher values for basalts than granites, in large part due to the presence of more divalent than monovalent cations in the primary minerals, tending to decrease rates of mineral dissolution. Weathering rates increase (as expected) with increasing CO2 and temperature. This modeling is done with the support of the Virtual Planetary Laboratory.

Applications of micro-spectroscopy and chemical imaging to delineate contaminant associations in heterogeneous mineral environments

International Nuclear Information System (INIS)

Hunter, D.

1998-01-01

Full text: Chemical speciation of a contaminant in the environment controls its mobility, bioavailability and ultimately its toxicity to organisms, including man. Transport models for environmental contaminants have continually failed because of an incomplete understanding of the physicochemical controls regulating the chemical speciation of both inorganic and organic contaminants. One of the greatest analytical difficulties to studying contaminant behavior in the subsurface is the inherent heterogeneity of mineral and organic constituents. Added to the multiplicity, of geological component surfaces that contaminants can interact with is the synergistic (both positive and negative) effects that occur due to non-conservative interactions between these components. Modern spectroscopic techniques can provide detailed quantitative and qualitative information on how contaminants behave within a specific mineral's surface-water interface. In general, the information is so rich as to be un interpretable in heterogeneous systems where multiple binding environments exist on competing multi-mineralic surfaces. None-the-less, it is the behaviour of contaminants in complex heterogeneous environments that is tantamount to understanding and predicting transport behaviour under field conditions. One solution is micro-spot spectroscopy. In micro-spot spectroscopy, chemical composition is determined by dispersing light absorbed or emitted from a highly localized spatial position within a heterogeneous sample. Such examples include FT-IR, Raman, fluorescence, and X-Ray absorption spectroscopies where spatial resolutions of 1 to 10 μm can be achieved. This scale can be still far too large to fully spectroscopically probe binding behaviour that is heterogeneous on colloidal scales ranging down to nanometers. However, it can provide a bridge to established characterization techniques such as optical petrography, since the challenge lies not only in identifying the speciation and

Mineral Fractionation during Sediment Comminution and Transport in Fluvio-Deltaic and Lacustrine Rocks of the Bradbury Group, Gale Crater, Mars

Science.gov (United States)

Siebach, K. L.; Baker, M. B.; Grotzinger, J. P.; McLennan, S. M.; Gellert, R.; Thompson, L. M.; Hurowitz, J.

2017-12-01

Mineral distribution patterns in sediments of the Bradbury group in Gale crater, interpreted from observations by the Mars Science Laboratory rover Curiosity, show the importance of transport mechanics in source-to-sink processes on Mars. The Bradbury group is comprised of basalt-derived mudstones to conglomerates exposed along the modern floor of Gale crater and analyzed along a 9-km traverse of the Curiosity rover. Over 110 bulk chemistry analyses of the rocks were acquired, along with two XRD mineralogical analyses of the mudstone. These rocks are uniquely suited for analysis of source-to-sink processes because they exhibit a wide range of compositions, but (based on multiple chemical weathering proxies) they appear to have experienced negligible cation-loss during weathering and erosion. Chemical variations between analyses correlate with sediment grain sizes, with coarser-grained rocks enriched in plagioclase components SiO2, Al2O3, and Na2O, and finer-grained rocks enriched in components of mafic minerals, consistent with grain-size sorting of mineral fractions during sediment transport. Further geochemical and mineralogical modeling supports the importance of mineral fractionation: even though the limited XRD data suggests that some fraction (if not all) of the rocks contain clays and an amorphous component, models show that 90% of the compositions measured are consistent with sorting of primary igneous minerals from a plagioclase-phyric subalkaline basalt (i.e., no corrections for cation-loss are required). The distribution of K2O, modeled as a potassium feldspar component, is an exception to the major-element trends because it does not correlate with grain size, but has an elevation-dependent signal likely correlated with the introduction of a second source material. However, the dominant compositional trends within the Bradbury group sedimentary rocks are correlated with grain size and consistent with mineral fractionation of minimally-weathered

Areal variation and chemical modification of weathered shale infiltration characteristics

International Nuclear Information System (INIS)

Luxmoore, R.J.; Spalding, B.P.; Munro, I.M.

1981-01-01

Spatial variability of infiltration into a weathered shale subsoil was evaluated at a site proximal to one used for shallow land burial of low-level radioactive waste at Oak Ridge National Laboratory. Double-ring infiltometers were installed at 48 locations on a 2- by 2-m grid after the removal of 1 to 2 m of soil (Litz-Sequoia association, Typic Hapludults). Infiltration rates were measured before and during the 0- to 20- and 239- to 259-day periods following treatment with solutions of NaOH, KOH, NaF, NaAlO 2 , and Na 2 SiO 3 at rates of 151 equivalents/m 2 . None of these chemical treatments significantly altered infiltration rate, indicating that chemical modification of soil exchange properties may be achieved without inducing hydrologic disturbance in these subsoils. A semivariogram analysis of infiltration data showed that areal variability was random; any spatial patterning must therefore occur at a smaller scale than 2 m

Mineralogical and geochemical trends in lateritic weathering profiles ...

African Journals Online (AJOL)

The absence of bauxite minerals like gibbsite and diaspora in the profiles shows that the trend of weathering is towards iron enrichment (ferralitization) and not aluminum accumulation (bauxitization). The CIA values of the lateritic layers shows that the weathering process is matured and has reached advanced stage.

Study on investigation and evaluation methods of deep seated sedimentary rocks. Chemical weathering, pore water squeezing and relationships of physical properties of sedimentary rocks

International Nuclear Information System (INIS)

Oyama, Takahiro; Suzuki, Koichi

2006-01-01

Chemical weathering, porewater squeezing and physical properties for the sedimentary rocks were examined. Chemical weathering potential of rocks was described by the sulfur as a acceleration factor of weathering and carbonate contents as a neutralization factor of it. The carbonate contents in the rocks were measured accurately by the gas pressure measurement method. Pore water squeezing method was applied for the semi-hard sedimentary rocks (Opalinusclay). The chemical change of extracted pore water under high pressure conditions was estimated. Physical property of sedimentary rocks have relationship among the porosity and permeability and resistivity coefficient in the same rock types. It is possible to estimate the water permeability from the geophysical tests. (author)

Chemical variation in hydrothermal minerals of the Los Humeros geothermal system, Mexico

Energy Technology Data Exchange (ETDEWEB)

Martinez-Serrano, R.G. [Universidad Nacional Autonoma de Mexico, Mexico, D.F. (Mexico). Insituto de Geofisica

2002-10-01

The Los Humeros geothermal system is composed of more than 2200 m of Quaternary altered volcanic rocks and an underlying Cretaceous sedimentary sequence. The low salinity of the fluids discharged at present (Na{sup +} and Cl{sup -} concentrations <500 ppm), and the excess steam, indicate that the reservoir contains a mixture of steam and dilute groundwater. Water-rock equilibrium is not attained. Hydrothermal minerals are present in veinlets, vugs, and replacing primary minerals. Three mineral zones are recognized: 1) a shallow argillic zone (<400 m depth), 2) a propylitic zone (ranging between 500 and 1800 m) and 3) a skarn zone (>1800 m). Petrographic examination of cuttings from five wells and temperature data indicate at least two stages of hydrothermal activity. Temperature is the main factor that affects the chemical composition of chlorite, epidote and biotite. Fe{sup 2+} and Al{sup IV} increase in chlorite with temperature [from 1.4 formula position unit (fpu) to 2.8, and from 0.7 to 2.4 fpu, respectively]. The pistacite content of epidote varies from 18 to 33 mol% in high-temperature regions (>270 {sup o}C) and from 13 to 26 mol% in low-temperature regions (<250 {sup 0}C). Biotite displays a slight increase in Al{sup IV} contents (1.55-2.8) and octahedral occupancy (5.93-6.0 fpu) with temperature. Whole rock composition and variations in oxygen fugacity condition are factors that also affect the concentrations of Fe, Al and Mg in the octahedral sites of chlorite, epidote, biotite and amphiboles. Chemical variations observed in alteration minerals at different depths in the Colapso Central-Xalapazco region could be used as indicator of relict physico-chemical conditions in the reservoir, before the present economic exploitation. (author)

Study on minerals status of dairy cows and their supplementation through area specific mineral mixture in the state of Jharkhand

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B. M. Bhanderi

2016-12-01

Full Text Available Abstract Background Deficiency of macro and micro-minerals in the ration of dairy cows adversely affects growth, milk production and reproduction efficiency. It is essential to examine mineral concentrations in feeds offered to dairy cows in practical farms. Methods Two villages from each taluka were selected at random for taking representative samples of feeds, forages and hair. Within the village, help was sought from village milk producers and district animal husbandry officer for identification of 4 to 5 farmers and collection of representative samples. All the samples were processed and analyzed for chemical composition as well as major macro and micro-minerals, using Inductively Coupled Plasma-Optical Emission Spectrometer. Results Ca content in wheat straw (0.29%, crushed maize (0.02% and wheat bran (0.12% was found to be below the critical level (0.30%. The P content in concentrate ingredients was high (0.26–0.96%, but low in dry roughages (0.06–0.12%. Cereal straws (0.14% and grains (0.12% were deficient in Mg. Feeds and forages were found to be adequate in K (1.50%. Cereals straws were found to be deficient in S (0.11%. Greens were good source of Cu (12.02 ppm. Wheat straw was found to be low in Zn (18 ppm, but high in Mn (225 ppm and Fe (509 ppm. Local grasses and azolla green were found to be rich source of Co (>1.00 ppm. Se (0.63 ppm was present in appreciable quantities in most of the feedstuffs. Conclusions From the present study, it was apparent that the feeds and forages available in the state of Jharkhand may not meet the requirements for Ca, P, Mg, Cu, Zn and Co in order to sustain a milk production of ~10 kg/day. Therefore, it is necessary to supplement these deficient minerals through area specific mineral mixture in the ration of dairy cows for improving productivity and reproduction efficiency.

Behaviour of elements in soils developed from nephelinites at Mount Etinde (Cameroon): Impact of hydrothermal versus weathering processes

Science.gov (United States)

Etame, J.; Gerard, M.; Bilong, P.; Suh, C. E.

2009-05-01

The progressive weathering of 0.65 Ma nephelinites from Mount Etinde (South Western Cameroon) in a humid tropical setting has resulted in the formation of a 150 cm thick weathering crust. The soil profiles consist of three horizons: Ah/Bw/C. A major differentiation of the chemical and mineralogical parameters is related to the complexity of the saprolites, some of which were hydrothermally altered. Bulk geochemical and microgeochemical analyses were performed on selected minerals from the different horizons of two reference profiles, of which one (E 4) was developed from unaltered nephelinite (nephelinite U) while the other (BO 1) formed from hydrothermally altered nephelinite (nephelinite H). The results show that the primary minerals (clinopyroxene, nepheline, leucite, haüyne, titanomagnetite, perovskite, apatite and sphene) experienced differential weathering rates with primary minerals rich in rare earth elements (titanomagnetite, perovskite, apatite and sphene) surviving in the saprolite and the Bw horizons. The weathering of the primary minerals is reflected in the leaching of alkaline and alkaline-earth elements, except for Ba and Rb in the hydrothermalised nephelinite soil. The order of mobility is influenced by hydrothermal processes: Na > K > Rb > Ca > Cs > Sr in nephelinite U soil , Na > K > Sr > Ca > Mg in nephelinite H soil; Rb/Sr and Sr/Mg can be used as indicators of the kinetic of the weathering on nephelinite U and on nephelinite H. Barium enrichment is related to variable concentrations in the nephelinites, to the formation of crandallites and the leaching of surface horizons. The content of metallic elements is higher in nephelinite H soil than in the nephelinite U soil. Results show that hydrothermal alteration leads to an enrichment of light (La, Ce, Nd) and intermediate (Sm, Eu, Dy) rare earth elements. The enrichment in Cr and Pb in the surface horizons is discussed in relation to organic matter activity, the dissolution of magnetites, and

Seafloor weathering buffering climate: numerical experiments

Science.gov (United States)

Farahat, N. X.; Archer, D. E.; Abbot, D. S.

2013-12-01

Continental silicate weathering is widely held to consume atmospheric CO2 at a rate controlled in part by temperature, resulting in a climate-weathering feedback [Walker et al., 1981]. It has been suggested that weathering of oceanic crust of warm mid-ocean ridge flanks also has a CO2 uptake rate that is controlled by climate [Sleep and Zahnle, 2001; Brady and Gislason, 1997]. Although this effect might not be significant on present-day Earth [Caldeira, 1995], seafloor weathering may be more pronounced during snowball states [Le Hir et al., 2008], during the Archean when seafloor spreading rates were faster [Sleep and Zahnle, 2001], and on waterworld planets [Abbot et al., 2012]. Previous studies of seafloor weathering have made significant contributions using qualitative, generally one-box, models, and the logical next step is to extend this work using a spatially resolved model. For example, experiments demonstrate that seafloor weathering reactions are temperature dependent, but it is not clear whether the deep ocean temperature affects the temperature at which the reactions occur, or if instead this temperature is set only by geothermal processes. Our goal is to develop a 2-D numerical model that can simulate hydrothermal circulation and resulting alteration of oceanic basalts, and can therefore address such questions. A model of diffusive and convective heat transfer in fluid-saturated porous media simulates hydrothermal circulation through porous oceanic basalt. Unsteady natural convection is solved for using a Darcy model of porous media flow that has been extensively benchmarked. Background hydrothermal circulation is coupled to mineral reaction kinetics of basaltic alteration and hydrothermal mineral precipitation. In order to quantify seafloor weathering as a climate-weathering feedback process, this model focuses on hydrothermal reactions that influence carbon uptake as well as ocean alkalinity: silicate rock dissolution, calcium and magnesium leaching

Practical Weathering for Geology Students.

Science.gov (United States)

Hodder, A. Peter

1990-01-01

The design and data management of an activity to study weathering by increasing the rate of mineral dissolution in a microwave oven is described. Data analysis in terms of parabolic and first-order kinetics is discussed. (CW)

Application of chemical tools to evaluate phytoremediation of weathered hydrocarbons

International Nuclear Information System (INIS)

Camp, H.; Kulakow, P.; Smart, D.R.; O'Reilly, K.

2002-01-01

The effectiveness of using phytoremediation methods to treat soils contaminated with hydrocarbons was tested in a three-year study at a site in northern California at a treatment pond for refinery process water. The treatment pond was drained several years ago and is targeted for cleanup. The petroleum hydrocarbons from the refinery waste were already highly degraded from natural weathering processes by the time the study began. The soil consists of about 23 per cent sand, 38 per cent silt, and 39 per cent clay. The study followed the Environmental Protection Agency's standardized field protocol and analytical approach. During the study, chemical data for several hydrocarbon parameters was gathered. Soil samples were Soxhlet-extracted in organic solvent and measured for oil and grease and total petroleum hydrocarbons using gravimetric techniques. One of the objectives was to develop an accurate quantitative way to identify sites and conditions where phytoremediation will be effective to supplement decision-tree-type approaches. The focus of the study is the application of chemical data in evaluating the effectiveness of the treatment process. Phytoremediation uses living plants for in situ remediation of polluted soils. The basic benefits of the techniques is that it is aesthetically pleasing, natural and passive. In addition, it is effective in cleaning up sites with low to moderate levels of pollution at shallow depths. A particular form of phytoremediation called rhizodegradation or enhanced rhizosphere biodegradation was the treatment used in this study. It is a treatment in which microorganisms digest organic substances and beak them down by biodegradation while being supported in the plant root structure. Test results indicate that the effects of phytoremediation treatments are subtle for highly weathered source material. It was noted that more statistical analysis will be performed with the data to determine compositional changes due to phytoremediation

The Specific Features of the Course of Critical Conditions in Miners

Directory of Open Access Journals (Sweden)

V. V. Moroz

2012-01-01

Full Text Available Objective: to improve treatment results in miners, by studying the specific features of the course of their critical conditions caused by severe traumatic injuries, and to develop differentiated intensive therapeutic regimens for detected abnormalities. Subjects and methods. A total of 1107 subjects were examined during the study. Central hemodynamic function was explored in 371 healthy miners with various lengths of underground mining; a control group included 30 healthy volunteers unexposed to occupational hazards. Examinations were made in 386 severe brain injury victims, including 218 victims with no length of underground work and 115 injured miners with an underground work length of more than 5 years. A control group comprised 53 apparently healthy donors. One hundred and twenty-two miners with severe thermal injury were examined. A control group consisted of 39 apparently healthy volunteers. One hundred and six victims with acute respiratory distress syndrome in the presence of severe concomitant injury were examined under mechanical ventilation. Sixty-three injured miners formed a study group; a comparison group included 43 subjects with no length of underground mining. Conclusion. Upon longer exposure to occupational hazards, the prenosological changes occur in the miners' organs and systems, which display a regular phasic pattern, fit in the picture of general adjustment syndrome, and determine the specific features of critical conditions. The peculiarities of the critical conditions caused by severe traumatic injuries in miners are the early development and high frequency of complications, the more severe course and late recovery of the body's lost functions, unlike the victims unexposed to occupational hazards. Differentiated intensive therapy for critical conditions in miners with severe traumatic injuries makes it possible to improve treatment results and to reduce death rates. 

Radioactivity of heavy minerals and geochemistry of trace elements and radon, resulting from the weathering of the ophiolitic complex, Northwest of Syria

International Nuclear Information System (INIS)

Kattaa, B.; Al-Hilal, M.; Jubeli, Y.

1999-06-01

Geochemical and radiometric survey of stream sediments resulting from the weathering of ophiolitic complex at Al-Basit area were carried out. Several exploration techniques have been used to evaluate the radioactive elements and minerals in the area, and to estimate the significance of the radioactivity of the source rocks of these elements and minerals. determination of radioelements and some trace elements in stream sediments, in addition to gamma-ray spectrometry and radon gas measurement in water of springs and wells were carried out in the study area. The results show that the high values of radioactive elements and radon concentration are related to the occurrence of syenite nepheline and plageogranite, characterized by higher content of these elements compared to mafic and ultramafic rocks. Mineralogical study of the heavy minerals shows that the abundant minerals are pyroxene and amphibole, while less abundant minerals are iron oxides (limonite and hematite), chromite, ilmenite, olivine and magnetite. Rare minerals are zircon, apatite, barite, tourmaline and sphen. The absence of monazite, xenotime and thorite in the collected samples is mainly attributed to the very limited occurrence of their source rocks. However, this results is rather restricted to the collected samples. High concentration of magnetite and ilmenite in some samples was noted, in addition to the presence of mineral called galaxite which was not reported previously. Gold flake was also found in one of the samples. The study of grain morphology suggests that the heavy minerals were transported for short distance from their source rocks. Grain size analyse of heavy minerals reveals that the concentration of economic minerals such as chromite and ilmenite increases with the decrease of the grain size. (author)

Ca isotopes, chemical weathering, and geomorphic controls on long-term climate

Science.gov (United States)

Moore, J.; Jacobson, A. D.; Holmden, C. E.; Craw, D.

2009-12-01

Calcium isotope geochemistry (δ44Ca) offers a unique opportunity to directly quantify proportions of riverine Ca originating from silicate versus carbonate weathering, which is essential for understanding how geomorphic processes affecting landscape evolution, such as tectonic uplift and glaciation, influence the long-term cycling of atmospheric CO2. We measured the elemental and δ44Ca chemistry of river and rock samples from the New Zealand Southern Alps. In combination with our geochemical data, we used runoff and suspended sediment fluxes to elucidate relationships between chemical weathering, mechanical erosion, and long-term climate. The S. Alps have uniform bedrock chemistry but significant tectonic and climatic gradients. West of the main topographic divide, watersheds drain schist and experience high runoff, uplift, and erosion rates. East of the main divide, watersheds drain greywacke or schist and experience lower runoff, uplift, and erosion rates. Glaciated watersheds with high erosion rates are present throughout the mountain range. Both schist and greywacke contain up to 3% metamorphic and hydrothermal calcite. Waters exhibit two-component mixing between calcite and silicate end-members when plotted as δ44Ca versus Ca/Sr. Scatter about the mixing curve is generally smaller than the analytical uncertainty of the measurements and likely reflects variability of the end-member compositions rather than fractionation. We used the mixing relationships to calculate percentages of Ca from silicate weathering. Rivers draining greywacke average 27.6% of Ca from silicate weathering with glaciated and non-glaciated watersheds yielding 41.8 and 19.5%, respectively. Rivers draining schist average 9.8% with glaciated and non-glaciated watersheds yielding 17.7 and 3.9%, respectively. Although Ca fluxes are larger west of the main divide where erosion and runoff are higher, the percentage of Ca from silicate weathering is smaller. Hence, long-term atmospheric CO2

Chemical-mineralogical study of the ferrosialitic lateritic profiles in the Teneme, Farallones and Cayo Guam sectors in north east Cuba

International Nuclear Information System (INIS)

Njila, Tendai; Diaz Martinez, Roberto

2016-01-01

The results of a chemical-mineralogical study on the ferrosialitic lateritic weathering profile are presented. Analysis was done using x Ray Fluorescence and Diffraction. The chemical composition of these profile reflects a typical pattern normally observed within such weathering crusts. The sesquioxides of aluminium, iron are concentrated in the upper parts of the profiles as a result of the leaching of alkalis, alkaline-earth elements, and to a lesser extent, silica. Ferrosialitic lateritic profiles formed on Cretaceous and Paleogene islands arcs consist of secondary minerals such as gibbsite, kaolinite, goethite, hematite and montmorillonite, while those associated with basic and volcanogenic-sedimentary rocks of ophiolitic affinity in Cayo Guam are composed of gibbsite and iron oxides. Brings new chemical-mineralogical information on the ferrosialitic lateritic profiles associated with rocks of oceanic nature in north-eastern Cuba, which will help in the exploration for industrial minerals and rocks and their application in industry. (author) [es

Strontium and cesium release mechanisms during unsaturated flow through waste-weathered Hanford sediments

International Nuclear Information System (INIS)

Chang, Hyun-Shik; Um, Wooyong; Rod, Kenton A.; Serne, R. Jeffrey; Thompson, Aaron; Perdrial, Nicolas; Steefel, Carl I.; Chorover, Jon

2011-01-01

Leaching behavior of Sr and Cs in the vadose zone of Hanford site (WA, USA) was studied with laboratory-weathered sediments mimicking realistic conditions beneath the leaking radioactive waste storage tanks. Unsaturated column leaching experiments were conducted using background Hanford pore water focused on first 200 pore volumes. The weathered sediments were prepared by 6 months reaction with a synthetic Hanford tank waste leachate containing Sr and Cs (10-5 and 10-3 molal representative of LO- and HI-sediment, respectively) as surrogates for 90Sr and 137Cs. The mineral composition of the weathered sediments showed that zeolite (chabazite-type) and feldspathoid (sodalite-type) were the major byproducts but different contents depending on the weathering conditions. Reactive transport modeling indicated that Cs leaching was controlled by ion-exchange, while Sr release was affected primarily by dissolution of the secondary minerals. The later release of K, Al, and Si from the HI-column indicated the additional dissolution of a more crystalline mineral (cancrinite-type). A two-site ion-exchange model successfully simulated the Cs release from the LO-column. However, a three-site ion-exchange model was needed for the HI-column. The study implied that the weathering conditions greatly impact the speciation of the secondary minerals and leaching behavior of sequestrated Sr and Cs.

The mineralogic evolution of the Martian surface through time: Implications from chemical reaction path modeling studies

Science.gov (United States)

Plumlee, G. S.; Ridley, W. I.; Debraal, J. D.; Reed, M. H.

1993-01-01

Chemical reaction path calculations were used to model the minerals that might have formed at or near the Martian surface as a result of volcano or meteorite impact driven hydrothermal systems; weathering at the Martian surface during an early warm, wet climate; and near-zero or sub-zero C brine-regolith reactions in the current cold climate. Although the chemical reaction path calculations carried out do not define the exact mineralogical evolution of the Martian surface over time, they do place valuable geochemical constraints on the types of minerals that formed from an aqueous phase under various surficial and geochemically complex conditions.

Crystal-Chemical Analysis Martian Minerals in Gale Crater

Science.gov (United States)

Morrison, S. M.; Downs, R. T.; Blake, D. F.; Bish, D. L.; Ming, D. W.; Morris, R. V.; Yen, A. S.; Chipera, S. J.; Treiman, A. H.; Vaniman, D. T.;

Phyllosilicate weathering pathways in chlorite-talc bearing soil parent materials, D.R. Congo: early findings.

Science.gov (United States)

Dumon, Mathijs; Oostermeyer, Fran; Timmermans, Els; De Meulemeester, Aschwin; Mees, Florias; Van Driessche, Isabel; Erens, Hans; Bazirake Mujinya, Basile; Van Ranst, Eric

2015-04-01

The study of the formation and transformation of clay minerals is of the upmost importance to understand soil formation and to adjust land-use management to the land surface conditions. These clay minerals determine to a large extent the soil physical and chemical properties. It is commonly observed that over time the mineralogy of any parent material is transformed to a simple assemblage composed mostly of Al and Fe oxides and low-activity clays, e.g. kaolinite. This is especially obvious in the humid tropics, which have been protected from glacial erosion, allowing deep, highly weathered soils to form. Despite the abundant presence of kaolinite in these soils, its formation pathways are still under debate: either neoformation by dissolution-crystallisation reactions or solid-state transformation of 2:1 phyllosilicates. To elucidate this, weathering sequences in a unique 40 m core taken below a termite mound, reaching a talc-chlorite bearing substrate in the Lubumbashi area, Katanga, DR Congo are being investigated in detail using a.o. quantitative X-ray diffraction analysis, chemical characterization, micromorphology and µXRF-scanning with the main objective to improve the understanding of the formation pathways of kaolinite subgroup minerals in humid tropical environments. Based on an initial characterization of the core, two zones of interest were selected for more detailed analysis, for which the early findings will be presented. The first zone extends from ca. 9 m to 11 m below the surface is dominated by kaolinite but shows early traces of primary talc and micas. The second zone extends from 34 to 36 m below the surface and contains large amounts of chlorite, with smaller amounts of talc, micas and kaolinite.

GEM-AQ, an on-line global multiscale chemical weather modelling system: model description and evaluation of gas phase chemistry processes

Directory of Open Access Journals (Sweden)

J. W. Kaminski

2008-06-01

Full Text Available Tropospheric chemistry and air quality processes were implemented on-line in the Global Environmental Multiscale weather prediction model. The integrated model, GEM-AQ, was developed as a platform to investigate chemical weather at scales from global to urban. The current chemical mechanism is comprised of 50 gas-phase species, 116 chemical and 19 photolysis reactions, and is complemented by a sectional aerosol module with 5 aerosols types. All tracers are advected using the semi-Lagrangian scheme native to GEM. The vertical transport includes parameterized subgrid-scale turbulence and large scale deep convection. Dry deposition is included as a flux boundary condition in the vertical diffusion equation. Wet deposition of gas-phase species is treated in a simplified way, and only below-cloud scavenging is considered. The emissions used include yearly-averaged anthropogenic, and monthly-averaged biogenic, ocean, soil, and biomass burning emission fluxes, as well as NO_x from lightning. In order to evaluate the ability to simulate seasonal variations and regional distributions of trace gases such as ozone, nitrogen dioxide and carbon monoxide, the model was run for a period of five years (2001–2005 on a global uniform 1.5°×1.5° horizontal resolution domain and 28 hybrid levels extending up to 10 hPa. Model results were compared with observations from satellites, aircraft measurement campaigns and balloon sondes. We find that GEM-AQ is able to capture the spatial details of the chemical fields in the middle and lower troposphere. The modelled ozone consistently shows good agreement with observations, except over tropical oceans. The comparison of carbon monoxide and nitrogen dioxide with satellite measurements emphasizes the need for more accurate, year-specific emissions fluxes for biomass burning and anthropogenic sources. Other species also compare well with available observations.

Rock weathering by indigenous heterotrophic bacteria of Bacillus spp. at different temperature: a laboratory experiment

Science.gov (United States)

Štyriaková, I.; Štyriak, I.; Oberhänsli, H.

2012-07-01

The bio-weathering of basalt, granite and gneiss was experimentally investigated in this study. These rock-forming minerals weathered more rapidly via the ubiquitous psychrotrophic heterotrophic bacteria . With indigenous bacteria of Bacillus spp. from sediments of Lake Baikal, we traced the degradation process of silicate minerals to understand the weathering processes occurring at the change temperature in the subsurface environment with organic input. The bacteria mediated dissolution of minerals was monitored with solution and solid chemistry, X-ray analyses as well as microscopic techniques. We determined the impact of the bacteria on the mineral surface and leaching of K, Ca, Mg, Si, Fe, and Al from silicate minerals. In the samples the release of major structural elements of silicates was used as an overall indicator of silicate mineral degradation at 4°C and 18°C from five medium exchanges over 255 days of rock bioleaching. The increase of temperature importantly affected the efficiency of Fe extraction from granite and basalt as well as Si extraction from granite and gneiss. In comparison with elemental extraction order at 4°C, Ca was substituted first by Fe or Si. It is evident that temperature influences rock microbial weathering and results in a change of elements extraction.

What's weathering? Mineralogy and field leach studies in mine waste, Leadville and Montezuma mining districts, Colorado

Science.gov (United States)

Diehl, S.F.; Hageman, Phil L.; Smith, Kathleen S.

2006-01-01

Weathering is important in the development of rock fabrics that control porosity in mine-waste materials, and in turn, porosity affects metal transport through and from mine-waste piles into watersheds. Mine-waste piles are dynamic physical and chemical systems as evidenced by remnant Fe-oxide boxwork structures after sulfide minerals, development of alteration rinds and etch pits on grains, and precipitation of secondary minerals under low temperature conditions. These microscale changes in the mine-waste materials are the result of partial to total dissolution of sulfide and other minerals. Mine-waste materials from the Dinero, Lower Chatauqua, and Saints John sites, Leadville and Montezuma mining districts, Colorado, exhibit rock fabrics that indicate that weathering products, e.g., Fe oxyhydroxides, jarosite, and clays, have been transported in suspension through the waste piles and deposited in voids and as coatings on rock fragments. Microscale characterization of weathered, partially dissolved minerals lends insight into the source of leachable metals in these mine-waste sites. Mineralogic studies show that galena in the Lower Chatauqua waste is enriched in Ag. Qualitative and semiquantitative microanalysis of weathered, altered galena grains from all three sites show that the Ag-bearing galena is more susceptible to dissolution. It is not surprising, then, that solutions experimentally leached from Lower Chatauqua waste are higher in Pb (2310 ppb) compared to leachates from the Dinero (31 ppb) and Saints John (1360 ppb) wastes. The mobility of metals is increased at acidic pH. Using the USGS Field Leach Test protocol, leachate derived from the Dinero waste has a pH of 3 and high concentrations of Al (443 ppb), Fe (441 ppb), and Zn (7970 ppb). Leachate from Sts. John tailings has a pH about 4 and high concentrations of Mn (1520 ppb), Zn (2240 ppb), and Pb (1360 ppb). Leachate from the Lower Chatauqua waste has an intermediate pH of 5, but in addition to the

Zeolite Formation and Weathering Processes in Dry Valleys of Antartica: Martian Analogs

Science.gov (United States)

Gibson, E. K., Jr.; Wentworth, S. J.; McKay, D. S.; Socki, R. A.

2004-01-01

Terrestrial weathering processes in cold-desert climates such as the Dry Valleys of Antarctica may provide an excellent analog to chemical weathering and diagenesis of soils on Mars. Detailed studies of soil development and the chemical and mineralogical alterations occurring within soil columns in Wright Valley, Antarctica show incredible complexity in the upper meter of soil. Previous workers noted the ice-free Dry Valleys are the best terrestrial approximations to contemporary Mars. Images returned from the Pathfinder and Spirit landers show similarities to surfaces observed within the Dry Valleys. Similarities to Mars that exist in these valleys are: mean temperatures always below freezing (-20 C), no rainfall, sparse snowfall-rapidly removed by sublimation, desiccating winds, diurnal freeze-thaw cycles (even during daylight hours), low humidity, oxidative environment, relatively high solar radiation and low magnetic fields . The Dry Valley soils contain irregular distributions and low abundances of soil microorganisms that are somewhat unusual on Earth. Physical processes-such as sand abrasion-are dominant mechanisms of rock weathering in Antarctica. However, chemical weathering is also an important process even in such extreme climates. For example, ionic migration occurs even in frozen soils along liquid films on individual soil particles. It has also been shown that water with liquid-like properties is present in soils at temperatures on the order of approx.-80 C and it has been observed that the percentage of oxidized iron increases with increasing soil age and enrichments in oxidized iron occurs toward the surface. The presence of evaporates is evident and appear similar to "evaporite sites" within the Pathfinder and Spirit sites. Evaporites indicate ionic migration and chemical activity even in the permanently frozen zone. The presence of evaporates indicates that chemical weathering of rocks and possibly soils has been active. Authogenic zeolites have

Mass-production of Cambro-Ordovician quartz-rich sandstone as a consequence of chemical weathering of Pan-African terranes: Environmental implications [rapid communication

Science.gov (United States)

Avigad, D.; Sandler, A.; Kolodner, K.; Stern, R. J.; McWilliams, M.; Miller, N.; Beyth, M.

2005-12-01

A vast sheet of mature quartz sand blanketed north Africa and Arabia from the Atlantic coast to the Persian Gulf in Cambro-Ordovician times. U-Pb geochronology of a representative section of Cambrian sandstone in southern Israel shows that these sediments are dominated by 550-650 Ma detrital zircons derived from Neoproterozoic Pan-African basement. The short time lag between magmatic consolidation of a Pan-African source and deposition of its erosional products indicates that, despite their significant mineralogical maturity, the voluminous quartz-rich sandstones on the northern margin of Gondwana are essentially first-cycle sediments. Mass production of these voluminous first-cycle quartz-rich sandstones resulted from widespread chemical weathering of the Pan-African continental basement. We suggest that conditions favoring silicate weathering, particularly a warm and humid climate, low relief and low sedimentation rates prevailed over large tracts of Gondwana in the aftermath of the Pan-African orogeny. An unusually corrosive Cambro-Ordovician atmosphere and humid climate enhanced chemical weathering on the vegetation-free landscape. We infer that late Neoproterozoic-Cambro-Ordovician atmospheric pCO 2 rose as a consequence of widespread late Neoproterozoic volcanism, followed by an uptake of CO 2 by chemical weathering to produce the Cambro-Ordovician sandstone as a negative feedback.

The effect of mechanical activation of cements with mineral ...

African Journals Online (AJOL)

... it comes that the increase of the specific surface and the chemical composition of cements to the mineral additions are the principal responsibles to the improvement of the latent reactivity of mineral additions and increase the mechanical strengths of the concretes. Journal of Civil Engineering Research and Practice Vol.

A geochemical record of the link between chemical weathering and the East Asian summer monsoon during the late Holocene preserved in lacustrine sediments from Poyang Lake, central China

Science.gov (United States)

Huang, Chao; Wei, Gangjian; Li, Wuxian; Liu, Ying

2018-04-01

This paper presents relatively high-resolution geochemical records spanning the past 4000 cal yr BP obtained from the lacustrine sediments of Poyang Lake in central China. The variations in the intensity of the East Asian summer monsoon (EASM) are traced using the K/Na, Ti/Na, Al/K, kaolinite/illite and clay/feldspar ratios, together with the chemical index of alteration (CIA), as indicators of chemical weathering. During the last 4000 years, the proxy records of chemical weathering from Poyang Lake exhibit an overall enhanced trend, consistent with regional hydrological changes in previous independent records. Further comparisons and analyses demonstrate that regional moisture variations in central China is inversely correlated with the EASM intensity, with weak EASM generating high precipitation in central China. Our data reveal three intervals of dramatically dry climatic conditions (i.e., ca. 4000-3200 cal yr BP, ca. 2800-2400 cal yr BP, and ca. 500-200 cal yr BP). A period of weak chemical weathering, related to cold and dry climatic conditions, occurred during the Little Ice Age (LIA), whereas more intense chemical weathering, reflecting warm and humid climatic conditions, was recorded during the Medieval Warm Period (MWP). Besides, an intensification of chemical weathering in Poyang Lake during the late Holocene agrees well with strong ENSO activity, suggesting that moisture variations in central China may be predominantly driven by ENSO variability.

Considering the Specific Impact of Harsh Conditions and Oil Weathering on Diversity, Adaptation, and Activity of Hydrocarbon-Degrading Bacteria in Strategies of Bioremediation of Harsh Oily-Polluted Soils

Science.gov (United States)

Al Disi, Zulfa; Jaoua, Samir; Al-Thani, Dhabia; Al-Meer, Saeed

2017-01-01

Weathering processes change properties and composition of spilled oil, representing the main reason of failure of bioaugmentation strategies. Our purpose was to investigate the metabolic adaptation of hydrocarbon-degrading bacteria at harsh conditions to be considered to overcome the limitations of bioaugmentation strategies at harsh conditions. Polluted soils, exposed for prolonged periods to weathered oil in harsh soils and weather conditions, were used. Two types of enrichment cultures were employed using 5% and 10% oil or diesel as sole carbon sources with varying the mineral nitrogen sources and C/N ratios. The most effective isolates were obtained based on growth, tolerance to toxicity, and removal efficiency of diesel hydrocarbons. Activities of the newly isolated bacteria, in relation to the microenvironment from where they were isoalted and their interaction with the weathered oil, showed individual specific ability to adapt when exposed to such factors, to acquire metabolic potentialities. Among 39 isolates, ten identified ones by 16S rDNA genes similarities, including special two Pseudomonas isolates and one Citrobacter isolate, showed particularity of shifting hydrocarbon-degrading ability from short chain n-alkanes (n-C12–n-C16) to longer chain n-alkanes (n-C21–n-C25) and vice versa by alternating nitrogen source compositions and C/N ratios. This is shown for the first time. PMID:28243605

Considering the Specific Impact of Harsh Conditions and Oil Weathering on Diversity, Adaptation, and Activity of Hydrocarbon-Degrading Bacteria in Strategies of Bioremediation of Harsh Oily-Polluted Soils

Directory of Open Access Journals (Sweden)

Zulfa Al Disi

2017-01-01

Full Text Available Weathering processes change properties and composition of spilled oil, representing the main reason of failure of bioaugmentation strategies. Our purpose was to investigate the metabolic adaptation of hydrocarbon-degrading bacteria at harsh conditions to be considered to overcome the limitations of bioaugmentation strategies at harsh conditions. Polluted soils, exposed for prolonged periods to weathered oil in harsh soils and weather conditions, were used. Two types of enrichment cultures were employed using 5% and 10% oil or diesel as sole carbon sources with varying the mineral nitrogen sources and C/N ratios. The most effective isolates were obtained based on growth, tolerance to toxicity, and removal efficiency of diesel hydrocarbons. Activities of the newly isolated bacteria, in relation to the microenvironment from where they were isoalted and their interaction with the weathered oil, showed individual specific ability to adapt when exposed to such factors, to acquire metabolic potentialities. Among 39 isolates, ten identified ones by 16S rDNA genes similarities, including special two Pseudomonas isolates and one Citrobacter isolate, showed particularity of shifting hydrocarbon-degrading ability from short chain n-alkanes (n-C12–n-C16 to longer chain n-alkanes (n-C21–n-C25 and vice versa by alternating nitrogen source compositions and C/N ratios. This is shown for the first time.

Identification of Uranium Minerals in Natural U-Bearing Rocks Using Infrared Reflectance Spectroscopy

Energy Technology Data Exchange (ETDEWEB)

Beiswenger, Toya N. [Pacific Northwest National Laboratory, Richland, WA, USA; Gallagher, Neal B. [Eigenvector Research, Inc., Manson, WA, USA; Myers, Tanya L. [Pacific Northwest National Laboratory, Richland, WA, USA; Szecsody, James E. [Pacific Northwest National Laboratory, Richland, WA, USA; Tonkyn, Russell G. [Pacific Northwest National Laboratory, Richland, WA, USA; Su, Yin-Fong [Pacific Northwest National Laboratory, Richland, WA, USA; Sweet, Lucas E. [Pacific Northwest National Laboratory, Richland, WA, USA; Lewallen, Tricia A. [Pacific Northwest National Laboratory, Richland, WA, USA; Johnson, Timothy J. [Pacific Northwest National Laboratory, Richland, WA, USA

2017-10-24

The identification of minerals, including uranium-bearing minerals, is traditionally a labor-intensive-process using x-ray diffraction (XRD), fluorescence, or other solid-phase and wet chemical techniques. While handheld XRD and fluorescence instruments can aid in field identification, handheld infrared reflectance spectrometers can also be used in industrial or field environments, with rapid, non-destructive identification possible via spectral analysis of the solid’s reflectance spectrum. We have recently developed standard laboratory measurement methods for the infrared (IR) reflectance of solids and have investigated using these techniques for the identification of uranium-bearing minerals, using XRD methods for ground-truth. Due to the rich colors of such species, including distinctive spectroscopic signatures in the infrared, identification is facile and specific, both for samples that are pure or are partially composed of uranium (e.g. boltwoodite, schoepite, tyuyamunite, carnotite, etc.) or non-uranium minerals. The method can be used to detect not only pure and partial minerals, but is quite sensitive to chemical change such as hydration (e.g. schoepite). We have further applied statistical methods, in particular classical least squares (CLS) and multivariate curve resolution (MCR) for discrimination of such uranium minerals and two uranium pure chemicals (U3O8 and UO2) against common background materials (e.g. silica sand, asphalt, calcite, K-feldspar) with good success. Each mineral contains unique infrared spectral features; some of the IR features are similar or common to entire classes of minerals, typically arising from similar chemical moieties or functional groups in the minerals: phosphates, sulfates, carbonates, etc. These characteristic 2 infrared bands generate the unique (or class-specific) bands that distinguish the mineral from the interferents or backgrounds. We have observed several cases where the chemical moieties that provide the

Mountain range specific analog weather forecast model for ...

Indian Academy of Sciences (India)

used to draw weather forecast for that mountain range in operational weather forecasting mode, three days ... various road management activities and for better .... −0.8. 1.5. 0.0. Pir Panjal range (HP). 1989–90 to 2002–03. 14. Snow day. 2.2. −4.1 ..... ed days,. S. = snow day,. N. S. = no-snow day and. P. C. = per cent correct).

Hydrokinesitherapy in thermal mineral water

Directory of Open Access Journals (Sweden)

Rendulić-Slivar Senka

2013-01-01

Full Text Available The treatment of clients in health spa resorts entails various forms of hydrotherapy. Due to specific properties of water, especially thermal mineral waters, hydrokinesitherapy has a positive effect on the locomotor system, aerobic capabilities of organism and overall quality of human life. The effects of use of water in movement therapy are related to the physical and chemical properties of water. The application of hydrotherapy entails precautionary measures, with an individual approach in assessment and prescription. The benefits of treatment in thermal mineral water should be emphasized and protected, as all thermal mineral waters differ in composition. All physical properties of water are more pronounced in thermal mineral waters due to its mineralisation, hence its therapeutical efficiency is greater, as well.

Chromium isotope fractionation during oxidative weathering of a modern basaltic weathering profile

DEFF Research Database (Denmark)

D'Arcy, Joan Mary; Døssing, Lasse Nørbye; Frei, Robert

Chromium can be used as a tracer of redox sensitive environmental processes. In soils Cr (III) is inert, immobile and resides predominantly in minerals, clays and oxides. Cr (VI) is toxic, soluble and mobile and is usually lost from the soil to local run off. Chromium isotopes have been shown...... to fractionate under both reducing and oxidizing conditions [1, 2]. Recent studies on d53Cr isotopes in laterite soils show that oxidative weathering of Cr-bearing rocks is accompanied by an isotopic fractionation, where by the lighter isotopes are retained in the residual soil and the heavier isotope...... is enriched in local runoff [1]. This study aims to quantify the stable Cr isotope composition of two modern basaltic weathering profiles, to help better understand the processes that oxidize inert Cr (III) to toxic Cr (VI). We sampled basaltic weathering profiles and associated river waters from areas of two...

Micro-scale novel stable isotope fractionation during weathering disclosed by femtosecond laser ablation

Science.gov (United States)

Schuessler, J. A.; von Blanckenburg, F.

2012-12-01

The stable isotope fractionation of metals and metalloids during chemical weathering and alteration of rocks at low temperature is a topic receiving increasing scientific attention. For these systems, weathering of primary minerals leads to selective partitioning of isotopes between the secondary minerals formed from them, and the dissolved phase of soil or river water. While the isotopic signatures of these processes have been mapped-out at the catchment or the soil scale, the actual isotopic fractionation is occurring at the mineral scale. To identify the processes underlying such micro-scale fractionation, the development of micro-analytical tools allows to investigate mechanisms of isotope fractionation in-situ, in combination with textural information of weathering reactions. We have developed a second-generation UV femtosecond (fs) laser system at GFZ Potsdam. The advantage of UV-fs laser ablation is the reduction of laser-induced isotopic and elemental fractionation by avoiding 'thermal effects' during ablation, such that accurate isotope ratios can be measured by standard-sample-standard bracketing using laser ablation multicollector ICP-MS; where the matrix of the bracketing standard does not need to match that of the sample [1]. Our system consists of the latest generation femtosecond solid-state laser (Newport Spectra Physics Solstice), producing an ultra short pulse width of about 100 femtoseconds at a wavelength of 196 nm. The system is combined with a custom-build computer-controlled sample stage and allows fully automated isotope analyses through synchronised operation of the laser with the Neptune MC-ICP-MS. To assess precision and accuracy of our laser ablation method, we analysed various geological reference materials. We obtained δ30Si values of -0.31 ± 0.23 (2SD, n = 13) for basalt glass BHVO-2G, and -1.25 ± 0.21 (2SD, n = 27) for pure Si IRMM17 when bracketed against NBS-28 quartz. δ56Fe and δ26Mg values obtained from non-matrix matched

Chemical analysis of minerals in granitic rocks by electron probe micro analyser

International Nuclear Information System (INIS)

Hiraoka, Yoshihiro

1994-01-01

The chemical compositions of minerals in a few granitic rocks were determined by electron probe micro analyser (EPMA). The accurate analytical data for standard feldspar groups were obtained by correcting the low analytical values of sodium and potassium that were arised from the damage in EPMA analysis. Using this method, feldspar groups and biotites in three granitic rocks gathered from Hiei, Hira and Kurama areas respectively, were analyzed. As the results, the local characteristics were observed in the kinds of feldspar groups and the chemical compositions of biotites that were contained in granitic rocks. (author)

Microbial and Chemical Enhancement of In-Situ Carbon Mineralization in Geological Formation

Energy Technology Data Exchange (ETDEWEB)

Matter, J.; Chandran, K.

2013-05-31

Predictions of global energy usage suggest a continued increase in carbon emissions and rising concentrations of CO{sub 2} in the atmosphere unless major changes are made to the way energy is produced and used. Various carbon capture and storage (CCS) technologies are currently being developed, but unfortunately little is known regarding the fundamental characteristics of CO{sub 2}-mineral reactions to allow a viable in-situ carbon mineralization that would provide the most permanent and safe storage of geologically-injected CO{sub 2}. The ultimate goal of this research project was to develop a microbial and chemical enhancement scheme for in-situ carbon mineralization in geologic formations in order to achieve long-term stability of injected CO{sub 2}. Thermodynamic and kinetic studies of CO{sub 2}-mineral-brine systems were systematically performed to develop the in-situ mineral carbonation process that utilizes organic acids produced by a microbial reactor. The major participants in the project are three faculty members and their graduate and undergraduate students at the School of Engineering and Applied Science and at the Lamont-Doherty Earth Observatory at Columbia University: Alissa Park in Earth and Environmental Engineering & Chemical Engineering (PI), Juerg Matter in Earth and Environmental Science (Co-PI), and Kartik Chandran in Earth and Environmental Engineering (Co-PI). Two graduate students, Huangjing Zhao and Edris Taher, were trained as a part of this project as well as a number of graduate students and undergraduate students who participated part-time. Edris Taher received his MS degree in 2012 and Huangjing Zhao will defend his PhD on Jan. 15th, 2014. The interdisciplinary training provided by this project was valuable to those students who are entering into the workforce in the United States. Furthermore, the findings from this study were and will be published in referred journals to disseminate the results. The list of the papers is given at

Weathering of the Rio Blanco Quartz Diorite, Luquillo Mountains, Puerto Rico: Coupling Oxidation, Dissolution, And Fracturing

International Nuclear Information System (INIS)

Buss, H.L.; Sak, P.B.; Webb, S.M.; Brantley, S.L.

2008-01-01

In the mountainous Rio Icacos watershed in northeastern Puerto Rico, quartz diorite bedrock weathers spheroidally, producing a 0.2-2 m thick zone of partially weathered rock layers (∼2.5 cm thickness each) called rindlets, which form concentric layers around corestones. Spheroidal fracturing has been modeled to occur when a weathering reaction with a positive ΔV of reaction builds up elastic strain energy. The rates of spheroidal fracturing and saprolite formation are therefore controlled by the rate of the weathering reaction. Chemical, petrographic, and spectroscopic evidence demonstrates that biotite oxidation is the most likely fracture-inducing reaction. This reaction occurs with an expansion in d (0 0 1) from 10.0 to 10.5 (angstrom), forming 'altered biotite'. Progressive biotite oxidation across the rindlet zone was inferred from thin sections and gradients in K and Fe(II). Using the gradient in Fe(II) and constraints based on cosmogenic age dates, we calculated a biotite oxidation reaction rate of 8.2 x 10 -14 mol biotite m -2 s -1 . Biotite oxidation was documented within the bedrock corestone by synchrotron X-ray microprobe fluorescence imaging and XANES. X-ray microprobe images of Fe(II) and Fe(III) at 2 (micro)m resolution revealed that oxidized zones within individual biotite crystals are the first evidence of alteration of the otherwise unaltered corestone. Fluids entering along fractures lead to the dissolution of plagioclase within the rindlet zone. Within 7 cm surrounding the rindlet-saprolite interface, hornblende dissolves to completion at a rate of 6.3 x 10 -13 mol hornblende m -2 s -1 : the fastest reported rate of hornblende weathering in the field. This rate is consistent with laboratory-derived hornblende dissolution rates. By revealing the coupling of these mineral weathering reactions to fracturing and porosity formation we are able to describe the process by which the quartz diorite bedrock disaggregates and forms saprolite. In the

Study of properties of chemically modified samples of halloysite mineral with X-ray fluorescence and X-ray powder diffraction methods

International Nuclear Information System (INIS)

Banaś, D.; Kubala-Kukuś, A.; Braziewicz, J.; Majewska, U.; Pajek, M.; Wudarczyk-Moćko, J.; Czech, K.; Garnuszek, M.; Słomkiewicz, P.; Szczepanik, B.

2013-01-01

Elemental and chemical composition of raw and activated samples of halloysite mineral using wavelength dispersive X-ray fluorescence (WDXRF), total reflection X-ray fluorescence (TXRF) and X-ray powder diffraction (XRPD) methods were determined. As the result, it has been shown that application of the complementary X-ray spectrometry techniques allows very precise observation of changes in composition of halloysite mineral samples caused by its chemical modifications. Sample preparation procedure and usability of the research methods applied are described in details. Procedure of activation of raw halloysite mineral samples by etching them in sulfuric acid of various concentrations has been described and discussed. The ability of the samples to adsorb lead from intentionally contaminated water was tested and confirmed. - Author-Highlights: • We measured elemental and chemical composition of raw and activated halloysite mineral samples. • We showed that X-ray techniques allow precise study of changes in the sample composition. • We describe procedure of activation of the samples by etching them in sulfuric acid. • We tested ability of halloysite mineral to absorb lead from contaminated water

Geochemical mass-balance to study the relative weathering rates of various formations in a complex watershed of lower Himalayas

Science.gov (United States)

Chattopadhyay, Pallavi; Kar, Swagat; Chouhan, Ramesh

2017-04-01

Weathering of rocks is a major process and believed to have the potential to alter Earth's surface. Aglar, a watershed in Garhwal Lesser Himalayas is identified and various formations of this complex geology are studied to understand the weathering process. A stream passes through the fault that divides the watershed into two slopes which have different lithotectonic units. Paligar and Belgar are the two main tributaries of Aglar stream flowing along the slopes respectively and joining at the valley near Thatyur village, India. Rocks like quartzite and limestone are generally hard, massive and resistant to weathering. However, sedimentary rocks are vulnerable to weathering and erosion. On the other hand, phyllites and schists are characterized by flaky minerals which weather quickly and promote instability . Aglar has all of them. The weathering processes are studied first using the hydrochemistry of Aglar river through major cations (Ca2+, Mg2+, Na+, K+) and major anions (SO42-, HCO-3, Cl-, NO3-). The discharges at various sampling points are calculated using area - velocity method. The basic idea in describing the discharge of material in a river is to estimate the mass of the substances transported through a cross section of the river per second. Dominance of Ca2+, Mg2+ and HCO-3 indicates that carbonate weathering is the major chemical weathering process near Belgar river. Paligar river has lower conductivity values compared to Belgar river which illustrates lower ionic concentrations. Mass-balance calculations are found often skewed and suggest the role of subsurface groundwater flow to explain the uncharacterized load. Southern side of the watershed with higher percentage of forest cover is found to have higher chemical weathering rates compared to the other slope having relatively lesser vegetation. These higher rates demonstrate the higher stream discharge load in that slope.

Advances in chemical and physical properties of electric arc furnace carbon steel slag by hot stage processing and mineral mixing

International Nuclear Information System (INIS)

Liapis, Ioannis; Papayianni, Ioanna

2015-01-01

Highlights: • Addition of 10% perlite decreases specific weight of the slag by approx. 7.5%. • Slag-crucible interaction and thin coating layer result in variations in XRF. • XRD shows high glass content and smaller crystalline sizes due to rapid cooling. • SEM shows higher homogeneity and lower crystallisation for SiO 2 /CaO-rich samples. • Physical properties (LA, PSV, AAV) of modified slag show limited deterioration. - Abstract: Slags are recognised as a highly efficient, cost effective tool in the metal processing industry, by minimising heat losses, reducing metal oxidation through contact with air, removing metal impurities and protecting refractories and graphite electrodes. When compared to natural aggregates for use in the construction industry, slags have higher specific weight that acts as an economic deterrent. A method of altering the specific weight of EAFC slag by hot stage processing and mineral mixing, during steel production is presented in this article. The method has minimal interference with the production process of steel, even by limited additions of appropriate minerals at high temperatures. Five minerals are examined, namely perlite, ladle furnace slag, bauxite, diatomite and olivine. Measurements of specific weight are accompanied by X-ray diffraction (XRD) and fluorescence (XRF) analysis and scanning electron microscopy spectral images. It is also shown how altering the chemical composition is expected to affect the furnace refractory lining. Additionally, the process has been repeated for the most suitable mix in gas furnace and physical properties (FI, SI, LA, PSV, AAV, volume stability) examined. Alteration of the specific weight can result in tailoring slag properties for specific applications in the construction sector

Advances in chemical and physical properties of electric arc furnace carbon steel slag by hot stage processing and mineral mixing

Energy Technology Data Exchange (ETDEWEB)

Liapis, Ioannis, E-mail: iliapis@sidenor.vionet.gr [AEIFOROS SA, 12th km Thessaloniki-Veroia Rd, PO Box 59, 57008 Ionia, Thessaloniki (Greece); Papayianni, Ioanna [Laboratory of Building Materials, Department of Civil Engineering, Aristotle University of Thessaloniki, 54124 Thessaloniki (Greece)

2015-02-11

Highlights: • Addition of 10% perlite decreases specific weight of the slag by approx. 7.5%. • Slag-crucible interaction and thin coating layer result in variations in XRF. • XRD shows high glass content and smaller crystalline sizes due to rapid cooling. • SEM shows higher homogeneity and lower crystallisation for SiO{sub 2}/CaO-rich samples. • Physical properties (LA, PSV, AAV) of modified slag show limited deterioration. - Abstract: Slags are recognised as a highly efficient, cost effective tool in the metal processing industry, by minimising heat losses, reducing metal oxidation through contact with air, removing metal impurities and protecting refractories and graphite electrodes. When compared to natural aggregates for use in the construction industry, slags have higher specific weight that acts as an economic deterrent. A method of altering the specific weight of EAFC slag by hot stage processing and mineral mixing, during steel production is presented in this article. The method has minimal interference with the production process of steel, even by limited additions of appropriate minerals at high temperatures. Five minerals are examined, namely perlite, ladle furnace slag, bauxite, diatomite and olivine. Measurements of specific weight are accompanied by X-ray diffraction (XRD) and fluorescence (XRF) analysis and scanning electron microscopy spectral images. It is also shown how altering the chemical composition is expected to affect the furnace refractory lining. Additionally, the process has been repeated for the most suitable mix in gas furnace and physical properties (FI, SI, LA, PSV, AAV, volume stability) examined. Alteration of the specific weight can result in tailoring slag properties for specific applications in the construction sector.

Global comparison reveals biogenic weathering as driven by nutrient limitation at ecosystem scale

Science.gov (United States)

Boy, Jens; Godoy, Roberto; Dechene, Annika; Shibistova, Olga; Amir, Hamid; Iskandar, Issi; Fogliano, Bruno; Boy, Diana; McCulloch, Robert; Andrino, Alberto; Gschwendtner, Silvia; Marin, Cesar; Sauheitl, Leopold; Dultz, Stefan; Mikutta, Robert; Guggenberger, Georg

2017-04-01

A substantial contribution of biogenic weathering in ecosystem nutrition, especially by symbiotic microorganisms, has often been proposed, but large-scale in vivo studies are still missing. Here we compare a set of ecosystems spanning from the Antarctic to tropical forests for their potential biogenic weathering and its drivers. To address biogenic weathering rates, we installed mineral mesocosms only accessible for bacteria and fungi for up to 4 years, which contained freshly broken and defined nutrient-baring minerals in soil A horizons of ecosystems along a gradient of soil development differing in climate and plant species communities. Alterations of the buried minerals were analyzed by grid-intersection, confocal lascer scanning microscopy, energy-dispersive X-ray spectroscopy, and X-ray photoelectron spectroscopy on the surface and on thin sections. On selected sites, carbon fluxes were tracked by 13C labeling, and microbial community was identified by DNA sequencing. In young ecosystems (protosoils) biogenic weathering is almost absent and starts after first carbon accumulation by aeolian (later litter) inputs and is mainly performed by bacteria. With ongoing soil development and appearance of symbiotic (mycorrhized) plants, nutrient availability in soil increasingly drove biogenic weathering, and fungi became the far more important players than bacteria. We found a close relation between fungal biogenic weathering and available potassium across all 16 forested sites in the study, regardless of the dominant mycorrhiza type (AM or EM), climate, and plant-species composition. We conclude that nutrient limitations at ecosystem scale are generally counteracted by adapted fungal biogenic weathering. The close relation between fungal weathering and plant-available nutrients over a large range of severely contrasting ecosystems points towards a direct energetic support of these weathering processes by the photoautotrophic community, making biogenic weathering a

Weathering of oils at sea: model/field data comparisons

International Nuclear Information System (INIS)

Daling, Per S.; Stroem, Tove

1999-01-01

The SINTEF Oil Weathering Model (OWM) has been extensively tested with results from full-scale field trials with experimental oil slicks in the Norwegian NOFO Sea trials in 1994 and 1995 and the AEA 1997 trials in UK. The comparisons between oil weathering values predicted by the model and ground-truth obtained from the field trials are presented and discussed. Good laboratory weathering data of the specific oil as input to the model is essential for obtaining reliable weathering predictions. Predications provided by the SINTEF-OWM enable oil spill personnel to estimate the most appropriate 'window of opportunity' for use of chemical dispersants under various spill situations. Pre-spill scenario analysis with the SINTEF Oil Spill Contingency and Response (OSCAR) model system, in which the SINTEF-OWM is one of several components, has become an important part of contingency plans as well as contingency training of oil spill personnel at refineries, oil terminals and offshore installations in Norway. (Author)

Chemical changes of minerals trapped in the lichen Trapelia involuta. Implication for lichen effect on mobility of uranium and toxic metals

International Nuclear Information System (INIS)

Kasama, Takeshi; Murakami, Takashi; Ohnuki, Toshihiko

2002-01-01

To elucidate development of minerals trapped in a lichen, we examined the lichen Trapelia involuta growing directly on secondary uranyl minerals and U-enriched Fe oxide and hydroxide minerals. Sericite and other minerals in the underlying rock are trapped in the lichen T. involuta during its biological growth and chemically changed by lichen activities. The presence of chemically changed sericite accompanied by an Fe-bearing mineral in the lichen suggests that dissolution of sericite is promoted mainly by polysaccharides excreted by the lichen. Oxalic acid or lichen acids absent in the medulla may not play an important role in the dissolution. Our results suggest that lichens on metal-rich surface affect the mobility of uranium and other toxic metals through dissolution followed by trap of minerals from the underlying rock. (author)

The natural weathering of staurolite: crystal-surface textures, relative stability, and the rate-determining step

Science.gov (United States)

Michael A. Velbel; Charles L. Basso; Michael J. Zieg

1996-01-01

Mineral surface-textures on naturally weathered crystals of staurolite [monoclinic, pseudo-orthorhombic; Fe4Al18Si8O46(OH)2] indicate that staurolite weathering is generally interface-limited. Etch pits on naturally weathered staurolites are disk-shaped,...

Copper leaching of MSWI bottom ash co-disposed with refuse: effect of short-term accelerated weathering.

Science.gov (United States)

Su, Lianghu; Guo, Guangzhai; Shi, Xinlong; Zuo, Minyu; Niu, Dongjie; Zhao, Aihua; Zhao, Youcai

2013-06-01

Co-disposal of refuse with municipal solid waste incinerator (MSWI) bottom ash (IBA) either multi-layered as landfill cover or mixed with refuse could pose additional risk to the environment because of enhanced leaching of heavy metals, especially Cu. This study applied short-term accelerated weathering to IBA, and monitored the mineralogical and chemical properties of IBA during the weathering process. Cu extractability of the weathered IBA was then evaluated using standard leaching protocols (i.e. SPLP and TCLP) and co-disposal leaching procedure. The results showed that weathering had little or no beneficial effect on Cu leaching in SPLP and TCLP, which can be explained by the adsorption and complexation of Cu with DOM. However, the Cu leaching of weathered IBA was reduced significantly when situated in fresh simulated landfill leachate. This was attributed to weakening Cu complexation with fulvic acid or hydrophilic fractions and/or intensifying Cu absorption to neoformed hydr(oxide) minerals in weathered IBA. The amount of total leaching Cu and Cu in free or labile complex fraction (the fraction with the highest mobility and bio-toxicity) of the 408-h weathered IBA were remarkably decreased by 86.3% and 97.6% in the 15-day co-disposal leaching test. Accelerated weathering of IBA may be an effective pretreatment method to decrease Cu leaching prior to its co-disposal with refuse. Copyright © 2013 Elsevier Ltd. All rights reserved.

Detecting Anthropogenic Disturbance on Weathering and Erosion Processes

Science.gov (United States)

Vanacker, V.; Schoonejans, J.; Bellin, N.; Ameijeiras-Mariño, Y.; Opfergelt, S.; Christl, M.

2014-12-01

Anthropogenic disturbance of natural vegetation can profoundly alter the physical, chemical and biological processes within soils. Rapid removal of topsoil during intense farming can result in an imbalance between soil production through chemical weathering and physical erosion, with direct implications on local biogeochemical cycling. However, the feedback mechanisms between soil erosion, chemical weathering and biogeochemical cycling in response to anthropogenic forcing are not yet fully understood. In this paper, we analyze dynamic soil properties for a rapidly changing anthropogenic landscape in the Spanish Betic Cordillera; and focus on the coupling between physical erosion, soil production and soil chemical weathering. Modern erosion rates were quantified through analysis of sediment deposition volumes behind check dams, and represent catchment-average erosion rates over the last 10 to 50 years. Soil production rates are derived from in-situ produced 10Be nuclide concentrations, and represent long-term flux rates. In each catchment, soil chemical weathering intensities were calculated for two soil-regolith profiles. Although Southeast Spain is commonly reported as the European region that is most affected by land degradation, modern erosion rates are low (140 t ha-1 yr-1). About 50 % of the catchments are losing soils at a rate of less than 60 t km-2 yr-1. Our data show that modern erosion rates are roughly of the same magnitude as the long-term or cosmogenically-derived erosion rates in the Betic Cordillera. Soils developed on weathered metamorphic rocks have no well-developed profile characteristics, and are generally thin and stony. Nevertheless, soil chemical weathering intensities are high; and question the occurrence of past soil truncation.

Effects of different mineral admixtures on the properties of fresh concrete.

Science.gov (United States)

Khan, Sadaqat Ullah; Nuruddin, Muhammad Fadhil; Ayub, Tehmina; Shafiq, Nasir

2014-01-01

This paper presents a review of the properties of fresh concrete including workability, heat of hydration, setting time, bleeding, and reactivity by using mineral admixtures fly ash (FA), silica fume (SF), ground granulated blast furnace slag (GGBS), metakaolin (MK), and rice husk ash (RHA). Comparison of normal and high-strength concrete in which cement has been partially supplemented by mineral admixture has been considered. It has been concluded that mineral admixtures may be categorized into two groups: chemically active mineral admixtures and microfiller mineral admixtures. Chemically active mineral admixtures decrease workability and setting time of concrete but increase the heat of hydration and reactivity. On the other hand, microfiller mineral admixtures increase workability and setting time of concrete but decrease the heat of hydration and reactivity. In general, small particle size and higher specific surface area of mineral admixture are favourable to produce highly dense and impermeable concrete; however, they cause low workability and demand more water which may be offset by adding effective superplasticizer.

Weathering and weathering rates of natural stone

Science.gov (United States)

Winkler, Erhard M.

1987-06-01

Physical and chemical weathering were studied as separate processes in the past. Recent research, however, shows that most processes are physicochemical in nature. The rates at which calcite and silica weather by dissolution are dependent on the regional and local climatic environment. The weathering of silicate rocks leaves discolored margins and rinds, a function of the rocks' permeability and of the climatic parameters. Salt action, the greatest disruptive factor, is complex and not yet fully understood in all its phases, but some of the causes of disruption are crystallization pressure, hydration pressure, and hygroscopic attraction of excess moisture. The decay of marble is complex, an interaction between disolution, crack-corrosion, and expansion-contraction cycies triggered by the release of residual stresses. Thin spalls of granites commonly found near the street level of buildings are generally caused by a combination of stress relief and salt action. To study and determine weathering rates of a variety of commercial stones, the National Bureau of Standards erected a Stone Exposure Test Wall in 1948. Of the many types of stone represented, only a few fossiliferous limestones permit a valid measurement of surface reduction in a polluted urban environment.

Controls on Weathering of Pyrrhotite in a Low-Sulfide, Granitic Mine-Waste Rock in the Canadian Arctic

Science.gov (United States)

Langman, J. B.; Holland, S.; Sinclair, S.; Blowes, D.

2013-12-01

Increased environmental risk is incurred with expansion of mineral extraction in the Arctic. A greater understanding of geochemical processes associated with hard-rock mining in this cold climate is needed to evaluate and mitigate these risks. A laboratory and in-situ experiment was conducted to examine mineral weathering and the generation of acid rock drainage in a low-sulfide, run-of-mine waste rock in an Arctic climate. Rock with different concentrations of sulfides (primarily pyrrhotite [Fe7S8] containing small amounts of Co and Ni) and carbonates were weathered in the laboratory and in-situ, large-scale test piles to examine leachate composition and mineral weathering. The relatively larger sulfide-containing rock produced sufficient acid to overcome carbonate buffering and produced a declining pH environment with concomitant release of SO4, Fe, Co, and Ni. Following carbonate consumption, aluminosilicate buffering stabilized the pH above 4 until a reduction in acid generation. Results from the laboratory experiment assisted in determining that after consumption of 1.6 percent of the total sulfide, the larger sulfide-concentration test pile likely is at an internal steady-state or maximal weathering rate after seven years of precipitation input and weathering that is controlled by an annual freeze-thaw cycle. Further weathering of the test pile should be driven by external factors of temperature and precipitation in this Arctic, semi-arid region instead of internal factors of wetting and non-equilibrium buffering. It is predicted that maximal weathering will continue until at least 20 percent of the total sulfide is consumed. Using the identified evolution of sulfide consumption in this Arctic climate, a variable rate factor can now be assessed for the possible early evolution and maximal weathering of larger scale waste-rock piles and seasonal differences because of changes in the volume of a waste-rock pile undergoing active weathering due to the freeze

Chemical, Mechanical, and Durability Properties of Concrete with Local Mineral Admixtures under Sulfate Environment in Northwest China.

Science.gov (United States)

Nie, Qingke; Zhou, Changjun; Shu, Xiang; He, Qiang; Huang, Baoshan

2014-05-13

Over the vast Northwest China, arid desert contains high concentrations of sulfate, chloride, and other chemicals in the ground water, which poses serious challenges to infrastructure construction that routinely utilizes portland cement concrete. Rapid industrialization in the region has been generating huge amounts of mineral admixtures, such as fly ash and slags from energy and metallurgical industries. These industrial by-products would turn into waste materials if not utilized in time. The present study evaluated the suitability of utilizing local mineral admixtures in significant quantities for producing quality concrete mixtures that can withstand the harsh chemical environment without compromising the essential mechanical properties. Comprehensive chemical, mechanical, and durability tests were conducted in the laboratory to characterize the properties of the local cementitious mineral admixtures, cement mortar and portland cement concrete mixtures containing these admixtures. The results from this study indicated that the sulfate resistance of concrete was effectively improved by adding local class F fly ash and slag, or by applying sulfate resistance cement to the mixtures. It is noteworthy that concrete containing local mineral admixtures exhibited much lower permeability (in terms of chloride ion penetration) than ordinary portland cement concrete while retaining the same mechanical properties; whereas concrete mixtures made with sulfate resistance cement had significantly reduced strength and much increased chloride penetration comparing to the other mixtures. Hence, the use of local mineral admixtures in Northwest China in concrete mixtures would be beneficial to the performance of concrete, as well as to the protection of environment.

Eco-chemical knowledge, behavior and engagement of workers employed in the mineral fertilizer industry in Novi Sad

Directory of Open Access Journals (Sweden)

Cvjetićanin Stanko

2006-01-01

Full Text Available The level of environmental pollution is influenced by the knowledge, behavior and ecological engagement of both the individual and society. The mineral fertilizer industry represents a potential source of pollution. The issue examined in this study is the level of eco-chemical knowledge, behavior and ecological engagement of the workers employed in the mineral fertilizer industry in Novi Sad. We have concluded that the workers hover low level of knowledge, behavior and engagement. The results obtained could be used for the selection of methods to enhance the eco-chemical knowledge of the employees.

Weathering profiles in granitoid rocks of the Sila Massif uplands, Calabria, southern Italy: New insights into their formation processes and rates

Science.gov (United States)

Scarciglia, Fabio; Critelli, Salvatore; Borrelli, Luigi; Coniglio, Sabrina; Muto, Francesco; Perri, Francesco

2016-05-01

In this paper we characterized several weathering profiles developed on granitoid rocks in the Sila Massif upland (Calabria, southern Italy), integrating detailed macro- and micromorphological observations with physico-mechanical field tests and petrographic, mineralogical and geochemical analyses. We focused our attention on the main weathering and pedogenetic processes, trying to understand apparent discrepancies between weathering grade classes based on field description and geomechanical properties, and two common weathering indices, such as the micropetrographic index (Ip) and the chemical index of alteration (CIA). Our results showed that sericite on plagioclase and biotite chloritization, that represent inherited features formed during late-stage hydrothermal alteration of granitoid rocks, may cause an overestimation of the real degree of weathering of primary mineral grains under meteoric conditions, especially in lower weathering grade classes. Moreover, the frequent identification of Fe-Mn oxides and clay coatings of illuvial origin (rather than or in addition to those formed in situ), both at the macro- and microscale, may also explain an overestimation of the weathering degree with respect to field-based classifications. Finally, some apparent inconsistencies between field geomechanical responses and chemical weathering were interpreted as related to physical weathering processes (cryoclastism and thermoclastism), that lead to rock breakdown even when chemical weathering is not well developed. Hence, our study showed that particular caution is needed for evaluating weathering grades, because traditional field and geochemical-petrographic tools may be biased by inherited hydrothermal alteration, physical weathering and illuvial processes. On the basis of chronological constraints to soil formation obtained from a 42 ka-old volcanic input (mixed to granite parent materials) detected in the soil cover of the Sila Massif upland, a first attempt to estimate

Chemical analyses of rocks, minerals, and detritus, Yucca Mountain--Preliminary report, special report No. 11

International Nuclear Information System (INIS)

Hill, C.A.; Livingston, D.E.

1993-09-01

This chemical analysis study is part of the research program of the Yucca Mountain Project intended to provide the State of Nevada with a detailed assessment of the geology and geochemistry of Yucca Mountain and adjacent regions. This report is preliminary in the sense that more chemical analyses may be needed in the future and also in the sense that these chemical analyses should be considered as a small part of a much larger geological data base. The interpretations discussed herein may be modified as that larger data base is examined and established. All of the chemical analyses performed to date are shown in Table 1. There are three parts to this table: (1) trace element analyses on rocks (limestone and tuff) and minerals (calcite/opal), (2) rare earth analyses on rocks (tuff) and minerals (calcite/opal), and (3) major element analyses + CO 2 on rocks (tuff) and detritus sand. In this report, for each of the three parts of the table, the data and its possible significance will be discussed first, then some overall conclusions will be made, and finally some recommendations for future work will be offered

Effect of chemical mixing state on the hygroscopicity and cloud nucleation properties of calcium mineral dust particles

Directory of Open Access Journals (Sweden)

R. C. Sullivan

2009-05-01

Full Text Available Atmospheric mineral dust particles can alter cloud properties and thus climate by acting as cloud condensation nuclei (CCN that form cloud droplets. The CCN activation properties of various calcium mineral dust particles were studied experimentally to investigate the consequences of field observations showing the segregation of sulphate from nitrate and chloride between individual aged Asian dust particles, and the enrichment of oxalic acid in Asian dust. Each mineral's observed apparent hygroscopicity was primarily controlled by its solubility, which determines the degree to which the mineral's intrinsic hygroscopicity can be expressed. The significant increase in hygroscopicity caused by mixing soluble hygroscopic material with insoluble mineral particles is also presented. Insoluble minerals including calcium carbonate, representing fresh unprocessed dust, and calcium sulphate, representing atmospherically processed dust, had similarly small apparent hygroscopicities. Their activation is accurately described by a deliquescence limit following the Kelvin effect and corresponded to an apparent single-hygroscopicity parameter, κ, of ~0.001. Soluble calcium chloride and calcium nitrate, representing atmospherically processed mineral dust particles, were much more hygroscopic, activating similar to ammonium sulphate with κ~0.5. Calcium oxalate monohydrate (κ=0.05 was significantly less CCN-active than oxalic acid (κ=0.3, but not as inactive as its low solubility would predict. These results indicate that the common assumption that all mineral dust particles become more hygroscopic and CCN-active after atmospheric processing should be revisited. Calcium sulphate and calcium oxalate are two realistic proxies for aged mineral dust that remain non-hygroscopic. The dust's apparent hygroscopicity will be controlled by its chemical mixing state, which is determined by its mineralogy and the chemical reaction pathways it experiences

Future Missions for Space Weather Specifications and Forecasts

Science.gov (United States)

Onsager, T. G.; Biesecker, D. A.; Anthes, R. A.; Maier, M. W.; Gallagher, F. W., III; St Germain, K.

2017-12-01

The progress of technology and the global integration of our economic and security infrastructures have introduced vulnerabilities to space weather that demand a more comprehensive ability to specify and to predict the dynamics of the space environment. This requires a comprehensive network of real-time space-based and ground-based observations with long-term continuity. In order to determine the most cost effective space architectures for NOAA's weather, space weather, and environmental missions, NOAA conducted the NOAA Satellite Observing System Architecture (NSOSA) study. This presentation will summarize the process used to document the future needs and the relative priorities for NOAA's operational space-based observations. This involves specifying the most important observations, defining the performance attributes at different levels of capability, and assigning priorities for achieving the higher capability levels. The highest priority observations recommended by the Space Platform Requirements Working Group (SPRWG) for improvement above a minimal capability level will be described. Finally, numerous possible satellite architectures have been explored to assess the costs and benefits of various architecture configurations.

Uranium fixation by mineralization at the redox front

International Nuclear Information System (INIS)

Isobe, Hiroshi

1998-01-01

The behavior of actinide elements including uranium in geomedia is controlled by redox conditions. Under the oxidized conditions, uranium forms uranyl ion (UO 2 2+ ) and its complexes, and dissolves in ground water. Under the reduced conditions, U(IV) has much lower solubility than uranyl ion. In the Koongarra uranium deposit, Australia, lead-bearing uraninite, uranyl lead oxide and uranyl silicate minerals occur in the unweathered, primary ore zone, and uranyl phosphate minerals occur in the weathered, secondary ore zone. Between unweathered and weathered zones, the transition zone exists as a redox front. In the transition zone, graphite and sulfide minerals react as reducing agents for species dissolved in ground water. By SEM, spherical grains of uraninite were observed in veins with graphite. Pyrite had coffinite rim with crystals of uraninite. Calculation based on the ground water chemistry and hydrology at Koongarra shows that the uranium in the transition zone may be fixed from the ground water. In the Koongarra transition zone, recent mineralization of uranium by reduction takes place. Mineralization is much stronger fixation mechanism than adsorption on clay minerals. Pyrite in the buffer materials of possible radioactive waste repositories can fix radionuclides in oxidized ground water by mineralization with reducing reactions. (author)

[Research on characteristics of soil clay mineral evolution in paddy field and dry land by XRD spectrum].

Science.gov (United States)

Zhang, Zhi-dan; Li, Qiao; Luo, Xiang-li; Jiang, Hai-chao; Zheng, Qing-fu; Zhao, Lan-po; Wang, Ji-hong

2014-08-01

The present paper took the typical saline-alkali soil in Jilin province as study object, and determinated the soil clay mineral composition characteristics of soil in paddy field and dry land. Then XRD spectrum was used to analyze the evolutionary mechanism of clay mineral in the two kinds of soil. The results showed that the physical and chemical properties of soil in paddy field were better than those in dry land, and paddy field would promote the weathering of mineral particles in saline-alkali soil and enhance the silt content. Paddy field soil showed a strong potassium-removal process, with a higher degree of clay mineral hydration and lower degree of illite crystallinity. Analysis of XRD spectrum showed that the clay mineral composition was similar in two kinds of soil, while the intensity and position of diffraction peak showed difference. The evolution process of clay mineral in dry land was S/I mixture-->vermiculite, while in paddy field it was S/I mixture-->vermiculite-->kaolinite. One kind of hydroxylated 'chlorite' mineral would appear in saline-alkali soil in long-term cultivated paddy field. Taking into account that the physical and chemical properties of soil in paddy field were better then those in dry land, we could know that paddy field could help much improve soil structure, cultivate high-fertility soil and improve saline-alkali soil. This paper used XRD spectrum to determine the characteristics of clay minerals comprehensively, and analyzed two'kinds of land use comparatively, and was a new perspective of soil minerals study.

Cross correlation of chemical profiles in minerals: insights into the architecture of magmatic reservoirs

Science.gov (United States)

Probst, Line; Caricchi, Luca; Gander, Martin; Wallace, Glenn

2016-04-01

Analysis of chemical zoning in minerals offers the opportunity to reconstruct the pre-eruptive conditions and the temporal evolution of magmatic reservoirs. The chemical composition of minerals is a function of the thermodynamic conditions of the reservoir from which they grow and therefore minerals record the evolution and variation of residual melt chemistry and intensive parameters within the magmatic system. A quantitative approach is required to determine if similar crystals actually shared a portion of their crystallisation history. These analyses are in many cases extremely time consuming and rather expensive. Therefore, it is not always possible to analyse a statically significant number of crystals, especially within their textural context in thin sections and that is the main reason to build automated methods. We are presenting a numerical cross-correlation method that compares the zonation pattern of minerals to identify if they share the totality or part of their growth history. We modified the method first developed by Wallace and Bergantz (2004) to compare profiles in minerals also from samples collected in different outcrops and that can be used for any dataset (i.e. geochemical proxies in stratigraphic sections). The main purpose of this method is to objectively compare chemical profiles in minerals (collected by electron microprobe, LA-ICP-MS or cathodoluminescence images) and quantify their degree of similarity. For this purpose, we use a well-known mathematical tool: the cross correlation which is a way of quantifying the difference between two given signals at a given position. Once our program was built, we performed tests using a set of synthetic profiles, profiles acquired along different transects of the same mineral and also on different minerals. Finally we applied our program to about 100 zircons from Kilgore Tuff, Heise Volcanic Field (USA) collected at different stratigraphic levels in two different outcrops. The correlation shows that

Raman and Fourier Transform Infrared (FT-IR) Mineral to Matrix Ratios Correlate with Physical Chemical Properties of Model Compounds and Native Bone Tissue.

Science.gov (United States)

Taylor, Erik A; Lloyd, Ashley A; Salazar-Lara, Carolina; Donnelly, Eve

2017-10-01

Raman and Fourier transform infrared (FT-IR) spectroscopic imaging techniques can be used to characterize bone composition. In this study, our objective was to validate the Raman mineral:matrix ratios (ν 1 PO 4 :amide III, ν 1 PO 4 :amide I, ν 1 PO 4 :Proline + hydroxyproline, ν 1 PO 4 :Phenylalanine, ν 1 PO 4 :δ CH 2 peak area ratios) by correlating them to ash fraction and the IR mineral:matrix ratio (ν 3 PO 4 :amide I peak area ratio) in chemical standards and native bone tissue. Chemical standards consisting of varying ratios of synthetic hydroxyapatite (HA) and collagen, as well as bone tissue from humans, sheep, and mice, were characterized with confocal Raman spectroscopy and FT-IR spectroscopy and gravimetric analysis. Raman and IR mineral:matrix ratio values from chemical standards increased reciprocally with ash fraction (Raman ν 1 PO 4 /Amide III: P Raman ν 1 PO 4 /Amide I: P Raman ν 1 PO 4 /Proline + Hydroxyproline: P Raman ν 1 PO 4 /Phenylalanine: P Raman ν 1 PO 4 /δ CH 2 : P Raman and IR mineral:matrix ratio values were strongly correlated ( P Raman mineral:matrix bone composition parameter correlates strongly to ash fraction and to its IR counterpart. Finally, the mineral:matrix ratio values of the native bone tissue are similar to those of both chemical standards and theoretical values, confirming the biological relevance of the chemical standards and the characterization techniques.

Weathering model for the quantification of atmospheric oxygen evolution during the Paleoproterozoic

Science.gov (United States)

Yokota, Kohei; Kanzaki, Yoshiki; Murakami, Takashi

2013-09-01

A weathering model has been developed to quantify atmospheric oxygen evolution during the Paleoproterozoic. The weathering model calculates the concentrations of Fe2+ dissolved from Fe2+-bearing primary minerals and oxidized Fe3+ out of the dissolved Fe2+ at a given partial pressure of atmospheric oxygen (PO2) during weathering and establishes the relationships between PO2 and ϕ, where ϕ is the ratio of oxidized and then precipitated Fe3+ out of the Fe2+ dissolved from primary minerals to the dissolved Fe2+ in a whole weathering profile. The weathering model considers controlling factors of the redistribution of Fe during weathering, that is, the dissolution rate of Fe2+-bearing primary minerals, the oxidation rate of Fe2+, and the groundwater flow rate. The validity of the model was confirmed by applying the model to the experimental data of olivine dissolution carried out under low O2 conditions. The sensitivity analysis of the model has revealed that the formation time of weathering, the mineral dissolution rate and the diffusion of O2 into a weathering profile have no or slight influence on ϕ, resulting in ˜0, 0 and 0.3 changes in log(PO2) caused by four orders of magnitude change of the formation time, more than 10 orders change of the mineral dissolution rate, and assumed change of the O2 diffusion, respectively. On the other hand, the temperature, the pH and the groundwater flow rate have moderate to large effects on ϕ: 0.6, 1.4 and 1.5 changes in log(PO2) for changes of 5 °C in temperature, 0.5 in pH, and one order of magnitude in groundwater flow rate, respectively. Using possible surface temperature, pH and groundwater flow rate estimated from the literature, we calculated the ϕ-PO2 relationships which were then applied to the ϕ values of paleosols (fossil weathering profiles) formed between 2.5 and 1.8 Ga. Taking account of the constraints given by the records of mass independent fractionation in sulfur isotopes and other geological proxies (i

Radiolysis of alanine adsorbed in a clay mineral

Energy Technology Data Exchange (ETDEWEB)

Aguilar-Ovando, Ellen Y.; Negron-Mendoza, Alicia [Instituto de Ciencias Nucleares, Universidad Nacional Autonoma de Mexico (UNAM), Circuito Exterior s/n, Ciudad Universitaria, Apartado Postal 70-543, Deleg. Coyoacan, C.P. 04510 (Mexico)

2013-07-03

Optical activity in molecules is a chemical characteristic of living beings. In this work, we examine the hypothesis of the influence of different mineral surfaces on the development of a specific chirality in organic molecules when subjected to conditions simulating the primitive Earth during the period of chemical evolution. By using X-ray diffraction techniques and HPLC/ELSD to analyze aqueous suspensions of amino acids adsorbed on minerals irradiated in different doses with a cobalt-60 gamma source, the experiments attempt to prove the hypothesis that some solid surfaces (like clays and meteorite rocks) may have a concentration capacity and protective role against external sources of ionizing radiation (specifically {gamma}-ray) for some organic compounds (like some amino acids) adsorbed on them. Preliminary results show a slight difference in the adsorption and radiolysis of the D-and L-alanine.

Radiolysis of alanine adsorbed in a clay mineral

International Nuclear Information System (INIS)

Aguilar-Ovando, Ellen Y.; Negrón-Mendoza, Alicia

2013-01-01

Optical activity in molecules is a chemical characteristic of living beings. In this work, we examine the hypothesis of the influence of different mineral surfaces on the development of a specific chirality in organic molecules when subjected to conditions simulating the primitive Earth during the period of chemical evolution. By using X-ray diffraction techniques and HPLC/ELSD to analyze aqueous suspensions of amino acids adsorbed on minerals irradiated in different doses with a cobalt-60 gamma source, the experiments attempt to prove the hypothesis that some solid surfaces (like clays and meteorite rocks) may have a concentration capacity and protective role against external sources of ionizing radiation (specifically γ-ray) for some organic compounds (like some amino acids) adsorbed on them. Preliminary results show a slight difference in the adsorption and radiolysis of the D-and L-alanine

Impacts of cold weather on all-cause and cause-specific mortality in Texas, 1990-2011.

Science.gov (United States)

Chen, Tsun-Hsuan; Li, Xiao; Zhao, Jing; Zhang, Kai

2017-06-01

Cold weather was estimated to account for more than half of weather-related deaths in the U.S. during 2006-2010. Studies have shown that cold-related excessive mortality is especially relevant with decreasing latitude or in regions with mild winter. However, only limited studies have been conducted in the southern U.S. The purpose of our study is to examine impacts of cold weather on mortality in 12 major Texas Metropolitan Areas (MSAs) for the 22-year period, 1990-2011. Our study used a two-stage approach to examine the cold-mortality association. We first applied distributed lag non-linear models (DLNM) to 12 major MSAs to estimate cold effects for each area. A random effects meta-analysis was then used to estimate pooled effects. Age-stratified and cause-specific mortalities were modeled separately for each MSA. Most of the MSAs were associated with an increased risk in mortality ranging from 0.1% to 5.0% with a 1 °C decrease in temperature below the cold thresholds. Higher increased mortality risks were generally observed in MSAs with higher average daily mean temperatures and lower latitudes. Pooled effect estimate was 1.58% (95% Confidence Interval (CI) [0.81, 2.37]) increase in all-cause mortality risk with a 1 °C decrease in temperature. Cold wave effects in Texas were also examined, and several MSAs along the Texas Gulf Coast showed statistically significant cold wave-mortality associations. Effects of cold on all-cause mortality were highest among people over 75 years old (1.86%, 95% CI [1.09, 2.63]). Pooled estimates for cause-specific mortality were strongest in myocardial infarction (4.30%, 95% CI [1.18, 7.51]), followed by respiratory diseases (3.17%, 95% CI [0.26, 6.17]) and ischemic heart diseases (2.54%, 95% CI [1.08, 4.02]). In conclusion, cold weather generally increases mortality risk significantly in Texas, and the cold effects vary with MSAs, age groups, and cause-specific deaths. Copyright © 2017 Elsevier Ltd. All rights reserved.

What is CCZN-armalcolite? A crystal-chemical discussion and an ad-hoc incursion in the crichtonite-minerals group

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Gavril Sabau

2007-10-01

Full Text Available The status of CCZN-armalcolite, commonly still believed to be a variety of armalcolite s.s., is questionable in view of partial evidence suggesting that it would represent a distinct phase, as initially claimed by its discoverers. Because of the rarity of the mineral, combined with its habitual small grain-size, no successful structural investigation could be undertaken so far. Therefore we attempted a chemical overview of existing and original data pertaining to CCZN-armalcolite. With the view of systematizing structure-composition relationships, we analyzed the topology of large cations – bearing close-packed oxides, while extending the nomenclature in use in order to accommodate further topologies. By using relevant chemical plots, a fair compositional match between CCZN-armalcolite and the crichtonite group minerals was demonstrated, as well as a chemical incompatibility with armalcolite. Stoichiometric crichtonite compositions and matching optical properties allowed identification of at least part of “CCZN-armalcolites” with the mineral loveringite of the crichtonite group. A detailed inspection of structure-composition relationships in crichtonites allowed an insight in their trends and range of chemical variation, as well as a comparison between them and a group of “CCZN-armalcolites” slightly differing from known crichtonites. These “CCZN-armalcolites” departing from normal chemical trends in crichtonites either represent an ordered variety of non-stoichiometric crichtonite or a new group of close-packed oxides. Their composition clustering around formula AM16O30 is temptingly consistent with an hypothetical structure intermediate between magnetoplumbites and crichtonites, based on close-packed stacking of layers made up by triangular clusters of octahedra, stuffed with large cations. A model of such a structure, not encountered so far in minerals, is outlined, displaying a hexagonal symmetry P , with a ≈ 7.45Å and c �

Calcium Isotope Fractionation during Carbonate Weathering in the Northern Guangdong, South China

Science.gov (United States)

Liu, F.; Mao, G.; Wei, G.; Zhang, Z.

2017-12-01

CO2 is consumed during the weathering of carbonates, whereas carbonates are precipitated rapidly in the oceans, which are pivotal to modulate atmospheric CO2, oceanic pH and climate. Calcium carbonate in limestone is one of the largest reservoirs of carbon at the Earth's surface, so calcium is an important element that links the lithosphere, hydrosphere, biosphere, and the atmosphere. Compared with silicate rocks, carbonate rocks have more rapid rates of physical and chemical erosions, so the carbonate weathering will respond more quickly to the climatic changes. In the southeast of China, enormous of carbonate rocks are widely distributed. Due to the influence of the subtropical monsoon climate, the rocks experienced strong chemical weathering and pedogenic process, resulting in red weathering crust of carbonate rocks. This type of weathering crust is geochemistry-sensitive and ecology-vulnerable, which can provide important insights into the recycle of supergene geochemistry in the karst areas. In this study, we report calcium isotopic compositions of saprolites from a weathering profile developed on argillaceous carbonate rocks in northern Guangdong, South China. The acid-leachable fraction, which was extracted by 1N hydrochloride acid, showed limited variation of δ44/40Ca(NIST 915a) spanning from 0.55 ± 0.06‰ (2SD) to 0.72 ± 0.05‰ (2SD) despite CaO content ranging from 0.01 wt.% to 45.7 wt.%, implying that Ca isotope didn't fractionate much which may due to the congruent dissolution of limestone minerals. In contrast, radiogenic 87Sr/86Sr ratios of the whole rocks changed with depth from 0.710086 ± 6 (2SE) at the base rock to 0.722164± 8 (2SE) at the top-soil, which are possibly attributed to the mixing effect between carbonate and silicate fractions. Sr is an analogue for Ca due to its similar ionic size and charge; however, these two systems can differ in certain respects. The coupled study of Ca and Sr will be helpful to verify sources of Ca and the

Age specific interactions between smoking and radon among United States uranium miners

International Nuclear Information System (INIS)

Steenland, K.

1994-01-01

United States uranium miners who smoked have death rates from lung cancer that are intermediate between the rates predicted by the additive and multiplicative models (on a ratio scale) across all age groups. Age specific patterns of interaction have not been thoroughly examined, and most analyses have been internal ones in which there was no truly non-exposed group. Here age specific death rates of lung cancer among ever smoking uranium miners have been examined for conformity with the additive and multiplicative models. The multiplicative model fits well for the youngest and oldest categories, but poorly for the middle age ranges. In the middle age range, predicted rates under the multiplicative model were quite high, surpassing the corresponding United States death rates for all causes combined. (Author)

Initiation of soil formation in weathered sulfidic Cu-Pb-Zn tailings under subtropical and semi-arid climatic conditions.

Science.gov (United States)

You, Fang; Dalal, Ram; Huang, Longbin

2018-08-01

Field evidence has been scarce about soil (or technosol) formation and direct phytostabilization of base metal mine tailings under field conditions. The present study evaluated key attributes of soil formation in weathered and neutral Cu-Pb-Zn tailings subject to organic amendment (WC: woodchips) and colonization of pioneer native plant species (mixed native woody and grass plant species) in a 2.5-year field trial under subtropical and semi-arid climatic conditions. Key soil indicators of engineered soil formation process were characterized, including organic carbon fractions, aggregation, microbial community and key enzymatic activities. The majority (64-87%) of the OC was stabilized in microaggregate or organo-mineral complexes in the amended tailings. The levels of OC and water soluble OC were elevated by 2-3 folds across the treatments, with the highest level in the treatment of WC and plant colonization (WC+P). Specifically, the WC+P treatment increased the proportion of water stable macroaggregates. Plants further contributed to the N rich organic matter in the tailings, favouring organo-mineral interactions and organic stabilization. Besides, the plants played a major role in boosting microbial biomass and activities in the treated tailings. WC and plants enhanced the contents of organic carbon (OC) associated with aggregates (e.g., physically protected OC), formation of water-stable aggregates (e.g., micro and macroaggregates), chemical buffering capacity (e.g., cation exchange capacity). Microbial community and enzymatic activities were also stimulated in the amended tailings. The present results showed that the formation of functional technosol was initiated in the eco-engineered and weathered Cu-Pb-Zn tailings under field conditions for direct phytostabilization. Copyright © 2018 Elsevier Ltd. All rights reserved.

40Ar/39Ar Geochronology of Supergene K-bearing Sulfate Minerals: Cenozoic Continental Weathering, Landscape Evolution and Paleoclimates in the Tu-Ha Basin, Northwestern China

Science.gov (United States)

Yang, J.; Zheng, D.; Chen, W.; Hough, B.; Qiu, H.; Wang, W.; Wu, Y.; Yang, L.

2017-12-01

40Ar/39Ar incremental-heating analyses of supergene jarosite and yavapaiite from three weathering profiles at the Hongshan, Liuhuangshan, and Caihuagou deposits in the Tu-Ha Basin, China, were carried out to provide numerical constraints on the timing and duration of weathering and derive insights into local paleoclimatic and landscape evolution. Well-constrained plateau ages and best-fitting inverse isochrons have been obtained for 11 samples, yield 40Ar/39Ar ages ranging from 33.3±0.5 Ma to 3.3±0.4 Ma (1σ). Our 40Ar/39Ar ages, combined with the published ages, indicate that the high elevations sites hosting the most complete and complex weathering profiles present. The presence of ancient weathering ages in current outcrop in the Tu-Ha Basin suggests that denudation was not homogeneous, and the landscape evolution follow a scarp retreat model. These geochronological results suggest that a protracted history of weathering and supergene enrichment and, by inference, arid-semiarid climate (with at least a moderate amount of precipitation (>10 cm/y)) favorable to intense chemical weathering emerged at 33.3 Ma, 27.7-23.3 Ma, and 16.4-14.7 Ma, and prevailed from 11-7.8 Ma. Then, a progressive change from arid-semiarid towards hyperarid conditions and predominantly hyperarid conditions may have persisted since at least ca. 3.3 Ma. The climatic implications inferred from the weathering geochronology are in agreement with the chemical parameters and isotopic compositions of the Cenozoic sedimentary sequence from the Lianmuqin section in the Tu-Ha Basin, attesting to the reliability of weathering geochronology by the 40Ar/39Ar method as an indicator of paleoclimate in arid areas. Our results suggest that the retreat of the Paratethys Sea, which would have reduced eastward water vapor transport by the westerlies to the Tu-Ha Basin, led to its aridification in the Oligocene and that increased rain shadow effects, resulting from uplift of the Tibetan Plateau and Tian Shan

Degradative crystal–chemical transformations of clay minerals under the influence of cyanobacterium-actinomycetal symbiotic associations

Directory of Open Access Journals (Sweden)

Ekaterina Ivanova

2014-04-01

Full Text Available Cyanobacteria and actinomycetes are essential components of soil microbial community and play an active role in ash elements leaching from minerals of the parent rock. Content and composition of clay minerals in soil determine the sorption properties of the soil horizons, water-holding capacity of the soil, stickiness, plasticity, etc. The transformative effect of cyanobacterial–actinomycetes associations on the structure of clay minerals – kaolinite, vermiculite, montmorillonite, biotite and muscovite – was observed, with the greatest structural lattice transformation revealed under the influence of association in comparison with monocultures of cyanobacterium and actinomycete. The range of the transformative effect depended both on the type of biota (component composition of association and on the crystal–chemical parameters of the mineral itself (trioctahedral mica – biotite, was more prone to microbial degradation than the dioctahedral – muscovite. The formation of the swelling phase – the product of biotite transformation into the mica–vermicullite mixed-layered formation was revealed as a result of association cultivation. Crystal chemical transformation of vermiculite was accompanied by the removal of potassium (К, magnesium (Mg and aluminum (Al from the crystal lattice. The study of such prokaryotic communities existed even in the early stages of the Earth's history helps to understand the causes and nature of the transformations undergone by the atmosphere, hydrosphere and lithosphere of the planet.contribution of treatments on structure induces and model parameters are discussed in the paper.

Study and interpretation of the chemical characteristics of natural water

Science.gov (United States)

Hem, John David

1985-01-01

The chemical composition of natural water is derived from many different sources of solutes, including gases and aerosols from the atmosphere, weathering and erosion of rocks and soil, solution or precipitation reactions occurring below the land surface, and cultural effects resulting from human activities. Broad interrelationships among these processes and their effects can be discerned by application of principles of chemical thermodynamics. Some of the processes of solution or precipitation of minerals can be closely evaluated by means of principles of chemical equilibrium, including the law of mass action and the Nernst equation. Other processes are irreversible and require consideration of reaction mechanisms and rates. The chemical composition of the crustal rocks of the Earth and the composition of the ocean and the atmosphere are significant in evaluating sources of solutes in natural freshwater.

Municipalities' Preparedness for Weather Hazards and Response to Weather Warnings.

Science.gov (United States)

Mehiriz, Kaddour; Gosselin, Pierre

2016-01-01

The study of the management of weather-related disaster risks by municipalities has attracted little attention even though these organizations play a key role in protecting the population from extreme meteorological conditions. This article contributes to filling this gap with new evidence on the level and determinants of Quebec municipalities' preparedness for weather hazards and response to related weather warnings. Using survey data from municipal emergency management coordinators and secondary data on the financial and demographic characteristics of municipalities, the study shows that most Quebec municipalities are sufficiently prepared for weather hazards and undertake measures to protect the population when informed of imminent extreme weather events. Significant differences between municipalities were noted though. Specifically, the level of preparedness was positively correlated with the municipalities' capacity and population support for weather-related disaster management policies. In addition, the risk of weather-related disasters increases the preparedness level through its effect on population support. We also found that the response to weather warnings depended on the risk of weather-related disasters, the preparedness level and the quality of weather warnings. These results highlight areas for improvement in the context of increasing frequency and/or severity of such events with current climate change.

Incorporating residual temperature and specific humidity in predicting weather-dependent warm-season electricity consumption

Science.gov (United States)

Guan, Huade; Beecham, Simon; Xu, Hanqiu; Ingleton, Greg

2017-02-01

Climate warming and increasing variability challenges the electricity supply in warm seasons. A good quantitative representation of the relationship between warm-season electricity consumption and weather condition provides necessary information for long-term electricity planning and short-term electricity management. In this study, an extended version of cooling degree days (ECDD) is proposed for better characterisation of this relationship. The ECDD includes temperature, residual temperature and specific humidity effects. The residual temperature is introduced for the first time to reflect the building thermal inertia effect on electricity consumption. The study is based on the electricity consumption data of four multiple-street city blocks and three office buildings. It is found that the residual temperature effect is about 20% of the current-day temperature effect at the block scale, and increases with a large variation at the building scale. Investigation of this residual temperature effect provides insight to the influence of building designs and structures on electricity consumption. The specific humidity effect appears to be more important at the building scale than at the block scale. A building with high energy performance does not necessarily have low specific humidity dependence. The new ECDD better reflects the weather dependence of electricity consumption than the conventional CDD method.

Modified clay minerals efficiency against chemical and biological warfare agents for civil human protection.

Science.gov (United States)

Plachá, Daniela; Rosenbergová, Kateřina; Slabotínský, Jiří; Kutláková, Kateřina Mamulová; Studentová, Soňa; Martynková, Gražyna Simha

2014-04-30

Sorption efficiencies of modified montmorillonite and vermiculite of their mono ionic Na and organic HDTMA and HDP forms were studied against chemical and biological warfare agents such as yperite and selected bacterial strains. Yperite interactions with modified clay minerals were observed through its capture in low-density polyethylene foil-modified clay composites by measuring yperite gas permeation with using chemical indication and gas chromatography methods. The antibacterial activities of synthetized organoclays were tested against selected Gram-positive and Gram-negative bacterial species in minimum inhibitory concentration tests. The obtained results showed a positive influence of modified clay minerals on the significant yperite breakthrough-time increase. The most effective material was the polyethylene-Na form montmorillonite, while the polyethylene-Na form vermiculite showed the lowest efficiency. With increasing organic cations loading in the interlayer space the montmorillonite efficiency decreased, and in the case of vermiculite an opposite effect was observed. Generally the modified montmorillonites were more effective than modified vermiculites. The HDP cations seem to be more effective compare to the HDTMA. The antibacterial activity tests confirmed efficiency of all organically modified clay minerals against Gram-positive bacteria. The confirmation of antibacterial activity against Y. pestis, plague bacteria, is the most interesting result of this part of the study. Copyright © 2014 Elsevier B.V. All rights reserved.

Organic and mineral fertilization and chemical composition of lemon balm (Melissa officinalis essential oil

Directory of Open Access Journals (Sweden)

Ana Carolina B. Sodré

2011-10-01

Full Text Available Melissa officinalis L., Lamiaceae, is an herb with great growth prospects in the cosmetic industry due to its essential oil. In order to improve its production, it is necessary to study related agricultural practices. This study evaluated the effect of organic and mineral fertilization on the chemical composition of lemon balm (Melissa officinalis L. essential oil. The assay was conducted at the "Fazenda Experimental do Glória" of the Federal University of Uberlândia, and essential oil extraction and GC/MS analyses were completed by the Centre for Research and Development on Plant Genetic Resources of the Campinas Agronomic Institute. The assay was conducted in a randomized complete block design with three replications. The tested treatments were six types of fertilization (0, 1, 2, 4, 8 kg.m-2 of cattle manure and mineral fertilizing with 60 g.m-2 of NPK 4-14-8 + 4 g.m-2 of boric acid with four replications. The essential oil was extracted by hydrodistillation in a modified Clevenger apparatus. The chemical composition was analyzed by GC/MS. The essential oil presented the same compounds for all treatments; however, the relative proportion of some chemical constituents was altered according to the treatment. Neral, geranial, and citronellal were the major constituents.

Organic and mineral fertilization and chemical composition of lemon balm (Melissa officinalis essential oil

Directory of Open Access Journals (Sweden)

Ana Carolina B. Sodré

2012-02-01

Full Text Available Melissa officinalis L., Lamiaceae, is an herb with great growth prospects in the cosmetic industry due to its essential oil. In order to improve its production, it is necessary to study related agricultural practices. This study evaluated the effect of organic and mineral fertilization on the chemical composition of lemon balm (Melissa officinalis L. essential oil. The assay was conducted at the "Fazenda Experimental do Glória" of the Federal University of Uberlândia, and essential oil extraction and GC/MS analyses were completed by the Centre for Research and Development on Plant Genetic Resources of the Campinas Agronomic Institute. The assay was conducted in a randomized complete block design with three replications. The tested treatments were six types of fertilization (0, 1, 2, 4, 8 kg.m-2 of cattle manure and mineral fertilizing with 60 g.m-2 of NPK 4-14-8 + 4 g.m-2 of boric acid with four replications. The essential oil was extracted by hydrodistillation in a modified Clevenger apparatus. The chemical composition was analyzed by GC/MS. The essential oil presented the same compounds for all treatments; however, the relative proportion of some chemical constituents was altered according to the treatment. Neral, geranial, and citronellal were the major constituents.

AWE: Aviation Weather Data Visualization Environment

Science.gov (United States)

Spirkovska, Lilly; Lodha, Suresh K.; Norvig, Peter (Technical Monitor)

2000-01-01

Weather is one of the major causes of aviation accidents. General aviation (GA) flights account for 92% of all the aviation accidents, In spite of all the official and unofficial sources of weather visualization tools available to pilots, there is an urgent need for visualizing several weather related data tailored for general aviation pilots. Our system, Aviation Weather Data Visualization Environment AWE), presents graphical displays of meteorological observations, terminal area forecasts, and winds aloft forecasts onto a cartographic grid specific to the pilot's area of interest. Decisions regarding the graphical display and design are made based on careful consideration of user needs. Integral visual display of these elements of weather reports is designed for the use of GA pilots as a weather briefing and route selection tool. AWE provides linking of the weather information to the flight's path and schedule. The pilot can interact with the system to obtain aviation-specific weather for the entire area or for his specific route to explore what-if scenarios and make "go/no-go" decisions. The system, as evaluated by some pilots at NASA Ames Research Center, was found to be useful.

The influence of condensed tannin structure on rate of microbial mineralization and reactivity to chemical assays.

Science.gov (United States)

Norris, Charlotte E; Preston, Caroline M; Hogg, Karen E; Titus, Brian D

2011-03-01

We examined how tannin structure influences reactivity in tannin assays and carbon and nitrogen mineralization. Condensed tannins from the foliage of ten tree and shrub species and from pecan shells (Carya illinoensis) had different proportions of: (a) epicatechin (cis) and catechin (trans) isomers, (b) procyanidin (PC) and prodelphinidin (PD) monomers, and (c) different chain lengths. The response of each tannin to several widely used tannin assays was determined. Although there was some variation in response to proanthocyanidin (butanol/HCl) and Folin Ciocalteu assays, we did not deduce any predictable relationship between tannin structure and response to either assay. There was little variation in protein precipitation among the different tannins. To assess biological activity, six of the tannins were incubated with forest humus for 22 days. We determined that, while PC-based tannins remained at least partly extractable for the duration of the incubation, tannins with a high proportion of PD subunits rapidly became unextractable from soil. There was a positive correlation between net nitrogen mineralization and cis chemical structure. Carbon mineralization was enhanced initially by the addition of tannins to humus, but after 22 days, a negative correlation between the proportion of cis subunits and respiration was determined. Overall, we were not able to demonstrate consistent effects of structure on either microbial mineralization or reactivity to chemical assays; such relationships remain elusive.

Surficial weathering of iron sulfide mine tailings under semi-arid climate.

Science.gov (United States)

Hayes, Sarah M; Root, Robert A; Perdrial, Nicolas; Maier, Raina; Chorover, Jon

2014-09-15

Mine wastes introduce anthropogenic weathering profiles to the critical zone that often remain unvegetated for decades after mining cessation. As such, they are vulnerable to wind and water dispersion of particulate matter to adjacent ecosystems and residential communities. In sulfide-rich ore tailings, propagation to depth of the oxidative weathering front controls the depth-variation in speciation of major and trace elements. Despite the prevalence of surficial mine waste deposits in arid regions of the globe, few prior studies have been conducted to resolve the near-surface profile of sulfide ore tailings weathered under semi-arid climate. We investigated relations between gossan oxidative reaction-front propagation and the molecular speciation of iron and sulfur in tailings subjected to weathering under semi-arid climate at an EPA Superfund Site in semi-arid central Arizona (USA). Here we report a multi-method data set combining wet chemical and synchrotron-based X-ray diffraction (XRD) and X-ray absorption near-edge spectroscopy (XANES) methods to resolve the tight coupling of iron (Fe) and sulfur (S) geochemical changes in the top 2 m of tailings. Despite nearly invariant Fe and S concentration with depth (130-140 and 100-120 g kg -1 , respectively), a sharp redox gradient and distinct morphological change was observed within the top 0.5 m, associated with a progressive oxidative alteration of ferrous sulfides to (oxyhydr)oxides and (hydroxy)sulfates. Transformation is nearly complete in surficial samples. Trends in molecular-scale alteration were co-located with a decrease in pH from 7.3 to 2.3, and shifts in Fe and S lability as measured via chemical extraction. Initial weathering products, ferrihydrite and gypsum, transform to schwertmannite, then jarosite-group minerals with an accompanying decrease in pH. Interestingly, thermodynamically stable phases such as goethite and hematite were not detected in any samples, but ferrihydrite was observed even in

Surficial weathering of iron sulfide mine tailings under semi-arid climate

Science.gov (United States)

Hayes, Sarah M.; Root, Robert A.; Perdrial, Nicolas; Maier, Raina M.; Chorover, Jon

2014-09-01

Mine wastes introduce anthropogenic weathering profiles to the critical zone that often remain unvegetated for decades after mining cessation. As such, they are vulnerable to wind and water dispersion of particulate matter to adjacent ecosystems and residential communities. In sulfide-rich ore tailings, propagation to depth of the oxidative weathering front controls the depth-variation in speciation of major and trace elements. Despite the prevalence of surficial mine waste deposits in arid regions of the globe, few prior studies have been conducted to resolve the near-surface profile of sulfide ore tailings weathered under semi-arid climate. We investigated relations between gossan oxidative reaction-front propagation and the molecular speciation of iron and sulfur in tailings subjected to weathering in a semi-arid climate at an EPA Superfund Site in central Arizona (USA). Here we report a multi-method data set combining wet chemical and synchrotron-based X-ray diffraction (XRD) and X-ray absorption near-edge spectroscopy (XANES) methods to resolve the tight coupling of iron (Fe) and sulfur (S) geochemical changes in the top 2 m of tailings. Despite nearly invariant Fe and S concentration with depth (130-140 and 100-120 g kg-1, respectively), a sharp redox gradient and distinct morphological change was observed within the top 0.5 m, associated with a progressive oxidative alteration of ferrous sulfides to (oxyhydr)oxides and (hydroxy)sulfates. Transformation is nearly complete in surficial samples. Trends in molecular-scale alteration were co-located with a decrease in pH from 7.3 to 2.3, and shifts in Fe and S lability as measured via chemical extraction. Initial weathering products, ferrihydrite and gypsum, transform to schwertmannite, then jarosite-group minerals with an accompanying decrease in pH. Interestingly, thermodynamically stable phases such as goethite and hematite were not detected in any samples, but ferrihydrite was observed even in samples with

Study on Mineral Weathering induced by Soil Ecosystem Engineers

OpenAIRE

阿部, 進

2016-01-01

研究成果の概要（和文）：本研究ではまず、土壌動物による鉱物風化作用に関する研究の現状と課題を明らかにするため、既往の研究のレビューを行った。また、ナイジェリア産のシロアリ塚土壌の試料を用いて、対照土壌との鉱物組成の比較を行なった結果、土壌動物が鉱物風化に及ぼす影響は小さいため、野外調査でその影響を定量的に調査することが難しいことを確認した。他方、熱帯の強風下土壌におけるシロアリの営巣活動に起因する遊離酸化鉱物の移動・集積が土壌生成過程で無視できない影響を及ぼすことを示唆した。この他、インドネシアの火山灰土壌地帯において、土地利用や管理主方が土壌動物相の変遷と非晶質鉱物の含有量に変化をもたらすことを明らかにした。研究成果の概要（英文）：First of all, the present study reviewed the literature on mineral weathering by soil fauna to highlight the current status and future challenges in this study topic. Then, the...

Chemical Force Spectroscopy Evidence Supporting the Layer-by-Layer Model of Organic Matter Binding to Iron (oxy)Hydroxide Mineral Surfaces

KAUST Repository

Chassé , Alexander W.; Ohno, Tsutomu; Higgins, Steven R.; Amirbahman, Aria; Yildirim, Nadir; Parr, Thomas B.

2015-01-01

© 2015 American Chemical Society. The adsorption of dissolved organic matter (DOM) to metal (oxy)hydroxide mineral surfaces is a critical step for C sequestration in soils. Although equilibrium studies have described some of the factors controlling this process, the molecular-scale description of the adsorption process has been more limited. Chemical force spectroscopy revealed differing adhesion strengths of DOM extracted from three soils and a reference peat soil material to an iron (oxy)hydroxide mineral surface. The DOM was characterized using ultrahigh-resolution negative ion mode electrospray ionization Fourier Transform ion cyclotron resonance mass spectrometry. The results indicate that carboxyl-rich aromatic and N-containing aliphatic molecules of DOM are correlated with high adhesion forces. Increasing molecular mass was shown to decrease the adhesion force between the mineral surface and the DOM. Kendrick mass defect analysis suggests that mechanisms involving two carboxyl groups result in the most stable bond to the mineral surface. We conceptualize these results using a layer-by-layer "onion" model of organic matter stabilization on soil mineral surfaces.

Chemical Force Spectroscopy Evidence Supporting the Layer-by-Layer Model of Organic Matter Binding to Iron (oxy)Hydroxide Mineral Surfaces

KAUST Repository

Chassé, Alexander W.

2015-08-18

© 2015 American Chemical Society. The adsorption of dissolved organic matter (DOM) to metal (oxy)hydroxide mineral surfaces is a critical step for C sequestration in soils. Although equilibrium studies have described some of the factors controlling this process, the molecular-scale description of the adsorption process has been more limited. Chemical force spectroscopy revealed differing adhesion strengths of DOM extracted from three soils and a reference peat soil material to an iron (oxy)hydroxide mineral surface. The DOM was characterized using ultrahigh-resolution negative ion mode electrospray ionization Fourier Transform ion cyclotron resonance mass spectrometry. The results indicate that carboxyl-rich aromatic and N-containing aliphatic molecules of DOM are correlated with high adhesion forces. Increasing molecular mass was shown to decrease the adhesion force between the mineral surface and the DOM. Kendrick mass defect analysis suggests that mechanisms involving two carboxyl groups result in the most stable bond to the mineral surface. We conceptualize these results using a layer-by-layer "onion" model of organic matter stabilization on soil mineral surfaces.

Effects of Climate on Co-evolution of Weathering Profiles and Hillscapes

Science.gov (United States)

Anderson, R. S.; Rajaram, H.; Anderson, S. P.

2017-12-01

Considerable debate revolves around the relative importance of rock type, tectonics, and climate in creating the architecture of the critical zone. It has recently been proposed that differences in the depths and patterns of weathering between landscapes in Colorado's Front Range and South Carolina's piedmont can be attributed to the state of stress in the rock imposed by the magnitude and orientation the regional stresses with respect to the ridgelines (St. Claire et al., 2016). We argue for the importance of the climate, and in particular, in temperate regions, the amount of recharge. We employ numerical models of hillslope evolution between bounding erosional channels, in which the degree of rock weathering governs the rate of transformation of rock to soil. As the water table drapes between the stream channels, fresh rock is brought into the weathering zone at a rate governed by the rate of incision of the channels. We track the chemical weathering of rock, represented by alteration of feldspar to clays, which in turn requires calculation of the concentration of reactive species in the water along hydrologic flow paths. We present results from analytic solutions to the flow field in which travel times can be efficiently assessed. Below the water table, flow paths are hyperbolic, taking on considerable lateral components as they veer toward the bounding channels that serve as drains to the hillslope. We find that if water is far from equilibrium with respect to weatherable minerals at the water table, as occurs in wet, slowly-eroding landscapes, deep weathering can occur well below the water table to levels approximating the base of the bounding channels. In dry climates, on the other hand, the weathering zone is limited to a shallow surface - parallel layer. These models capture the essence of the observed differences in depth to fresh rock in both wet and dry climates without appeal to the state of stress in the rock.

Using High-Precision Specific Gravity Measurements to Study Minerals in Undergraduate Geoscience Courses

Science.gov (United States)

Brandriss, Mark E.

2010-01-01

This article describes ways to incorporate high-precision measurements of the specific gravities of minerals into undergraduate courses in mineralogy and physical geology. Most traditional undergraduate laboratory methods of measuring specific gravity are suitable only for unusually large samples, which severely limits their usefulness for student…

Using Weather Types to Understand and Communicate Weather and Climate Impacts

Science.gov (United States)

Prein, A. F.; Hale, B.; Holland, G. J.; Bruyere, C. L.; Done, J.; Mearns, L.

2017-12-01

A common challenge in atmospheric research is the translation of scientific advancements and breakthroughs to decision relevant and actionable information. This challenge is central to the mission of NCAR's Capacity Center for Climate and Weather Extremes (C3WE, www.c3we.ucar.edu). C3WE advances our understanding of weather and climate impacts and integrates these advances with distributed information technology to create tools that promote a global culture of resilience to weather and climate extremes. Here we will present an interactive web-based tool that connects historic U.S. losses and fatalities from extreme weather and climate events to 12 large-scale weather types. Weather types are dominant weather situations such as winter high-pressure systems over the U.S. leading to very cold temperatures or summertime moist humid air masses over the central U.S. leading to severe thunderstorms. Each weather type has a specific fingerprint of economic losses and fatalities in a region that is quantified. Therefore, weather types enable a direct connection of observed or forecasted weather situation to loss of life and property. The presented tool allows the user to explore these connections, raise awareness of existing vulnerabilities, and build resilience to weather and climate extremes.

Kinetically limited weathering at low denudation rates in semi-arid climates

Science.gov (United States)

Vanacker, V.; Schoonejans, J.; Opfergelt, S.; Ameijeiras-Marino, Y.; Christl, M.

2016-12-01

On Earth, the Critical Zone supports terrestrial life, being the near-surface environment where interactions between the atmosphere, lithosphere, hydrosphere, and biosphere take place Quantitative understanding of the interaction between mechanical rock breakdown, chemical weathering, and physical erosion is essential for unraveling Earth's biogeochemical cycles. In this study, we explore the role of soil water balance on regulating soil chemical weathering under water deficit regimes. Weathering rates and intensities were evaluated for nine soil profiles located on convex ridge crests of three mountain ranges in the Spanish Betic Cordillera. We present and compare quantitative information on soil weathering, chemical depletion and total denudation that were derived based on geochemical mass balance, 10Be cosmogenic nuclides and U-series disequilibria. Soil production rates determined based on U-series isotopes (238U, 234U, 230Th and 226Ra) are of the same order of magnitude as 10Be-derived denudation rates, suggesting steady state soil thickness, in two out of three sampling sites. The chemical weathering intensities are relatively low (˜5 to 30% of the total denudation of the soil) and negatively correlated with the magnitude of the water deficit in soils. Soil weathering extents increase (nonlinearly) with soil thickness and decrease with increasing surface denudation rates, consistent with kinetically limited or controlled weathering. Our study suggests that soil residence time and water availability limit weathering processes in semi-arid climates, which has not been validated previously with field data. An important implication of this finding is that climatic regimes may strongly regulate soil weathering by modulating soil solute fluxes.

A Comparative Analyses of Granulometry, Mineral Composition and Major and Trace Element Concentrations in Soils Commonly Ingested by Humans

Directory of Open Access Journals (Sweden)

Veronica M. Ngole-Jeme

2015-07-01

Full Text Available This study compared the granulometric properties, mineralogical composition and concentrations of major and trace element oxides of commonly ingested soils (geophagic soil collected from different countries with a view of understanding how varied they may be in these properties and to understand the possible health implications of ingesting them. Soil samples were collected from three different countries (South Africa, Swaziland and Democratic Republic of Congo (DRC and their granulometric properties, concentrations of major and trace element oxides as well as mineralogical composition determined. Differences were observed in the granulometric properties of geophagic soil from the three different countries with most of them having <20% clay content. The soils also showed varied degrees of weathering with values of Chemical Index of Alteration (CIA and Chemical Index of Weathering (CIW being between 60% and 99.9% respectively. The mineral assemblages of the soils from South Africa and Swaziland were dominated by the primary minerals quartz and feldspar whereas soils from DRC had more of kaolinite, a secondary mineral than primary minerals. Soils from DRC were associated with silt, clay, Al2O3, and CIA unlike most samples from South Africa which were associated with SiO2, sand, K2O, CaO, and MgO. The soils from Swaziland were closely associated with silt, H2O and Fe2O3(t. These associations reflect the mineralogy of the samples. These soils are not likely to serve as nutrient supplements because of the low concentrations of the nutrient elements contained. The coarse texture of the samples may also result in dental destruction during mastication. Sieving of the soils before ingestion to remove coarse particles is recommended to reduce the potential health threat associated with the ingestion of coarse-textured soils.

A Comparative Analyses of Granulometry, Mineral Composition and Major and Trace Element Concentrations in Soils Commonly Ingested by Humans

Science.gov (United States)

Ngole-Jeme, Veronica M.; Ekosse, Georges-Ivo E.

2015-01-01

This study compared the granulometric properties, mineralogical composition and concentrations of major and trace element oxides of commonly ingested soils (geophagic soil) collected from different countries with a view of understanding how varied they may be in these properties and to understand the possible health implications of ingesting them. Soil samples were collected from three different countries (South Africa, Swaziland and Democratic Republic of Congo (DRC)) and their granulometric properties, concentrations of major and trace element oxides as well as mineralogical composition determined. Differences were observed in the granulometric properties of geophagic soil from the three different countries with most of them having soils also showed varied degrees of weathering with values of Chemical Index of Alteration (CIA) and Chemical Index of Weathering (CIW) being between 60% and 99.9% respectively. The mineral assemblages of the soils from South Africa and Swaziland were dominated by the primary minerals quartz and feldspar whereas soils from DRC had more of kaolinite, a secondary mineral than primary minerals. Soils from DRC were associated with silt, clay, Al2O3, and CIA unlike most samples from South Africa which were associated with SiO2, sand, K2O, CaO, and MgO. The soils from Swaziland were closely associated with silt, H2O and Fe2O3(t). These associations reflect the mineralogy of the samples. These soils are not likely to serve as nutrient supplements because of the low concentrations of the nutrient elements contained. The coarse texture of the samples may also result in dental destruction during mastication. Sieving of the soils before ingestion to remove coarse particles is recommended to reduce the potential health threat associated with the ingestion of coarse-textured soils. PMID:26264010

Calcium weathering in forested soils and the effedt of different tree species

NARCIS (Netherlands)

Dijkstra, F.A.; Breemen, van N.; Jongmans, A.G.; Davies, G.R.; Likens, G.E.

2003-01-01

Soil weathering can be an important mechanism to neutralize acidity in forest soils. Tree species may differ in their effect on or response to soil weathering. We used soil mineral data and the natural strontium isotope ratio Sr-87/Sr-86 as a tracer to identify the effect of tree species on the Ca

Chemical and radiochemical specifications - PWR power plants

International Nuclear Information System (INIS)

Stutzmann, A.

1997-01-01

Published by EDF this document gives the chemical specifications of the PWR (Pressurized Water Reactor) nuclear power plants. Among the chemical parameters, some have to be respected for the safety. These parameters are listed in the STE (Technical Specifications of Exploitation). The values to respect, the analysis frequencies and the time states of possible drops are noticed in this document with the motion STE under the concerned parameter. (A.L.B.)

Developing biogeochemical tracers of apatite weathering by ectomycorrhizal fungi

Science.gov (United States)

Vadeboncoeur, M. A.; Bryce, J. G.; Hobbie, E. A.; Meana-Prado, M. F.; Blichert-Toft, J.

2012-12-01

Chronic acid deposition has depleted calcium (Ca) from many New England forest soils, and intensive harvesting may reduce phosphorus (P) available to future rotations. Thin glacial till soils contain trace amounts of apatite, a primary calcium phosphate mineral, which may be an important long-term source of both P and Ca to ecosystems. The extent to which ECM fungi enhance the weathering rate of primary minerals in soil which contain growth-limiting nutrients remains poorly quantified, in part due to biogeochemical tracers which are subsequently masked by within-plant fractionation. Rare earth elements (REEs) and Pb isotope ratios show some potential for revealing differences in soil apatite weathering rates across forest stands and silvicultural treatments. To test the utility of these tracers, we grew birch seedlings semi-hydroponically under controlled P-limited conditions, supplemented with mesh bags containing granite chips. Our experimental design included nonmycorrhizal (NM) as well as ectomycorrhizal cultures (Cortinarius or Leccinum). Resulting mycorrhizal roots and leachates of granite chips were analyzed for these tracers. REE concentrations in roots were greatly elevated in treatments with granite relative to those without granite, demonstrating uptake of apatite weathering products. Roots with different mycorrhizal fungi accumulated similar concentrations of REEs and were generally elevated compared to the NM cultures. Ammonium chloride leaches of granite chips grown in contact with mycorrhizal hyphae show elevated REE concentrations and significantly radiogenic Pb isotope signatures relative to bulk rock, also supporting enhanced apatite dissolution. Our results in culture are consistent with data from field-collected sporocarps from hardwood stands in the Bartlett Experimental Forest in New Hampshire, in which Cortinarius sporocarp Pb isotope ratios were more radiogenic than those of other ectomycorrhizal sporocarps. Taken together, the experimental

Chemical cleaning specification: few tube test model

International Nuclear Information System (INIS)

Hampton, L.V.; Simpson, J.L.

1979-09-01

The specification is for the waterside chemical cleaning of the 2 1/4 Cr - 1 Mo steel steam generator tubes. It describes the reagents and conditions for post-chemical cleaning passivation of the evaporator tubes

Amorphous silica maturation in chemically weathered clastic sediments

Science.gov (United States)

Liesegang, Moritz; Milke, Ralf; Berthold, Christoph

2018-03-01

A detailed understanding of silica postdepositional transformation mechanisms is fundamental for its use as a palaeobiologic and palaeoenvironmental archive. Amorphous silica (opal-A) is an important biomineral, an alteration product of silicate rocks on the surface of Earth and Mars, and a precursor material for stable silica phases. During diagenesis, amorphous silica gradually and gradationally transforms to opal-CT, opal-C, and eventually quartz. Here we demonstrate the early-stage maturation of several million year old opal-A from deeply weathered Early Cretaceous and Ordovician sedimentary rocks of the Great Artesian Basin (central Australia). X-ray diffraction, scanning electron microscopy, and electron probe microanalyses show that the mineralogical maturation of the nanosphere material is decoupled from its chemical properties and begins significantly earlier than micromorphology suggests. Non-destructive and locally highly resolved X-ray microdiffraction (μ-XRD2) reveals an almost linear positive correlation between the main peak position (3.97 to 4.06 Å) and a new asymmetry parameter, AP. Heating experiments and calculated diffractograms indicate that nucleation and growth of tridymite-rich nanodomains induce systematic peak shifts and symmetry variations in diffraction patterns of morphologically juvenile opal-A. Our results show that the asymmetry parameter traces the early-stage maturation of amorphous silica, and that the mineralogical opal-A/CT stage extends to smaller d-spacings and larger FWHM values than previously suggested.

Iron isotopic fractionation during continental weathering

Energy Technology Data Exchange (ETDEWEB)

Fantle, Matthew S.; DePaolo, Donald J.

2003-10-01

The biological activity on continents and the oxygen content of the atmosphere determine the chemical pathways through which Fe is processed at the Earth's surface. Experiments have shown that the relevant chemical pathways fractionate Fe isotopes. Measurements of soils, streams, and deep-sea clay indicate that the {sup 56}Fe/{sup 54}Fe ratio ({delta}{sup 56}Fe relative to igneous rocks) varies from +1{per_thousand} for weathering residues like soils and clays, to -3{per_thousand} for dissolved Fe in streams. These measurements confirm that weathering processes produce substantial fractionation of Fe isotopes in the modern oxidizing Earth surface environment. The results imply that biologically-mediated processes, which preferentially mobilize light Fe isotopes, are critical to Fe chemistry in weathering environments, and that the {delta}{sup 56}Fe of marine dissolved Fe should be variable and negative. Diagenetic reduction of Fe in marine sediments may also be a significant component of the global Fe isotope cycle. Iron isotopes provide a tracer for the influence of biological activity and oxygen in weathering processes through Earth history. Iron isotopic fractionation during weathering may have been smaller or absent in an oxygen-poor environment such as that of the early Precambrian Earth.

Deep Soil Carbon in the Critical Zone: Amount and Nature of Carbon in Weathered Bedrock, and its Implication for Soil Carbon Inventory

Science.gov (United States)

Moreland, K. C.; Tian, Z.; Berhe, A. A.; O'Geen, A. T.

2017-12-01

Globally, soils store more carbon (C) than the vegetation and the atmosphere combined. Up to 60-80% of the C stored in soils is found in below 30cm soil depth, but there is little data on C storage in weathered bedrock or saprolite. Deep soil organic matter (SOM) can be a mixture of new and old SOM; that is rendered relatively stable due to burial, aggregation, its disconnection from decomposers, and chemical association that organic matter forms with soil minerals. The limited data available on deep SOM dynamics suggests that stock, distribution, and composition of deep SOM are strongly correlated to climate. The overall objective of this research is to investigate how climate regulates OM storage, composition, stability, and stabilization mechanisms. Expecting that the amount of OM stored in deep soil and the stability are a function of soil thickness and availability of weathering products (i.e. reactive minerals), the stock and stability of deep SOM is expected to follow a similar relationship with climate, as does the intensity of weathering. This research is conducted in the NSF funded Southern Sierra Critical Zone Observatories that is located along a climosequence, the western slopes of the Sierra Naevada Mountains of California. Here we will present results derived from characterization of soils and weathered bedrock using elemental and stable isotope elemental analysis, and Fourier Transformed Infrared Spectroscopy to determine OM concentration and functional group level composition of bulk SOM. Our findings show that adding in subsoil and weathered bedrock C stocks increases estimates of soil C stock by 1/3rd to 2/3rd.

Cave breakdown by vadose weathering.

Directory of Open Access Journals (Sweden)

Osborne R. Armstrong L.

2002-01-01

Full Text Available Vadose weathering is a significant mechanism for initiating breakdown in caves. Vadose weathering of ore bodies, mineral veins, palaeokarst deposits, non-carbonate keystones and impure, altered or fractured bedrock, which is intersected by caves, will frequently result in breakdown. Breakdown is an active, ongoing process. Breakdown occurs throughout the vadose zone, and is not restricted to large diameter passages, or to cave ceilings. The surfaces of disarticulated blocks are commonly coated, rather than having fresh broken faces, and blocks continue to disintegrate after separating from the bedrock. Not only gypsum, but also hydromagnesite and aragonite are responsible for crystal wedging. It is impossible to study or identify potential breakdown foci by surface surveys alone, in-cave observation and mapping are essential.

A Weighty Subject: Exploration for Heavy Minerals Across the State of Mississippi

Science.gov (United States)

Gifford, J.; Woolsey, A. I.; Yarbrough, L. D.; Platt, B. F.; Widanagamage, I. H.; Easson, G. L.

2017-12-01

collection is needed to confirm if heavy mineral enrichment is related to specific geomorphologic features, depositional features, or a combination of weathering specific source material at particular times in the geologic record.

Chemical analysis of mineral water available in the local markets of Pakistan

International Nuclear Information System (INIS)

Iqbal, M.A.; Zaib, S.; Sher, N.; Tariq, S.

2009-01-01

Chemical analysis of mineral water of different companies was carried out asses the quality of mineral water available in the local market. The results were compared with WHO standards. Na/sup +/ and K/sup +/ were determined with the help of flame emissions spectrophotometer while Cl/sup 1/, HCO/sub 3/, Ca/sup +2/ and Mg/sup +2/ were determined by titrimetric methods. The physical parameters such as pH, EC, and TDS were determined by pH meter, EC meter and TDS meter respectively. It was observed that about 80 percentage of the sample obey the WHO standards regarding Na/sup +/ and K/sup +/ whereas only 20 percentage samples fall within the permissible limit regarding Cl/sup -/ ions. The concentration of Ca/sup +2/ in all the sample exceeds the permissible limits. It was concluded that some brands need to improve their quality. (author)

Uranium mineralization by ground water in sedimentary rocks, Japan

International Nuclear Information System (INIS)

Doi, K.; Hirono, S.; Sakamaki, Y.

1975-01-01

To solve the mechanism of uranium concentration in stratabound uranium deposits occurring in the basal part of Neogene sediments overlying granite basement, attention was paid to uranium leaching from weathered granite by circulating carbonated fissure waters, to effective adsorbents for fixing uranium from uraniferous ground waters, to structural features controlling the ground-water circulation, and other relevant factors. The evidence for uranium transportation by hydothermal solutions, including hot spring waters, is hard to observe. Conclusions are summarized as follows: Uranium in the deposits is supplied from surrounding source rocks, mostly from granite. Uranium is transported by circulating ground-water solutions. The uranium dissolved in ground water is fixed in minerals in various ways, the most important being adsorption by carbonaceous matter. Ore-grade uranium concentrated from very dilute solutions occurs by multiple repetition of a leaching-and-fixation cycle between minerals or adsorbents and circulating uraniferous ground water. Important factors for uranium mineralization are sufficient uranium, supplied mostly from granite, the existence of effective adsorbents such as carbonaceous matter in the host rocks, and favorable geological, geochemical, and geophysical environments. The last seem to require not only physical and chemical conditions but also correct flow and volume of ground water. (U.S.)

The effect of weathering on the distribution of uranium and associated elements at Koongarra, Northern Territory, Australia

International Nuclear Information System (INIS)

Edis, Robert

1992-03-01

The aim of work described in this thesis was to investigate some aspects of the redistribution of U and other elements, at the Koongarra No.1 U ore deposit in the Northern Territory of Australia. Aspects of the redistribution of U which are considered in this thesis include the spatial patterns of remobilised U; the associations of U with minerals and elements and how these change with weathering, and transport of material by colloids present in the groundwater. The Koongarra No.1 U ore deposit is currently being studied as a natural analogue of a high level radioactive waste repository, as part of the Alligator Rivers Analogue Project. As spent fuel is a proposed waste form for geological burial, the study of uraninite leaching in an ore body makes a very good analogue of a breached repository. Work presented in this thesis was undertaken as part of that study. Aspects of the redistribution considered here include spatial patterns of redistributed U, associations between U, other elements and minerals, and transport of material by groundwater colloids. Techniques employed include:- thin section analyses (optical analysis, autoradiography, electron microprobe, and scanning electron microscopy); mineralogical and chemical analyses (x-ray diffraction, x-ray fluorescence, PIXE-PIGME, neutron activation, and infra-red spectrophotometry); groundwater colloid sampling and concentrating (tangential and stirred cell ultrafiltration); transmission electron microscopy for the examination of colloids and scanning electron microscopy for the examination of prefilters. The redistribution of U during weathering appeared to follow the distribution of Fe oxides. Uranium present in the groundwater responsible for the weathering would then have absorbed onto the freshly precipitated and highly sorptive Fe oxides. Uranium concentrations appeared to be correlative to the degree of weathering, and the corresponding amount of Fe oxides. 339 refs., 36 tabs., 83 figs

Mercury's Weather-Beaten Surface: Understanding Mercury in the Context of Lunar and Asteroidal Space Weathering Studies

Science.gov (United States)

Domingue, Deborah L.; Chapman, Clark. R.; Killen, Rosemary M.; Zurbuchen, Thomas H.; Gilbert, Jason A.; Sarantos, Menelaos; Benna, Mehdi; Slavin, James A.; Schriver, David; Travnicek, Pavel M.;

The nanosphere iron mineral(s) in Mars soil

Science.gov (United States)

Banin, A.; Ben-Shlomo, T.; Margulies, L.; Blake, D. F.; Mancinelli, R. L.; Gehring, A. U.

1993-01-01

A series of surface-modified clays containing nanophase (np) iron/oxyhydroxides of extremely small particle sizes, with total iron contents as high as found in Mars soil, were prepared by iron deposition on the clay surface from ferrous chloride solution. Comprehensive studies of the iron mineralogy in these 'Mars-soil analogs' were conducted using chemical extractions, solubility analyses, pH and redox, x ray and electron diffractometry, electron microscopic imaging specific surface area and particle size determinations, differential thermal analyses, magnetic properties characterization, spectral reflectance, and Viking biology simulation experiments. The clay matrix and the procedure used for synthesis produced nanophase iron oxides containing a certain proportion of divalent iron, which slowly converts to more stable, fully oxidized iron minerals. The noncrystalline nature of the iron compounds precipitated on the surface of the clay was verified by their complete extractability in oxalate. Lepidocrocite (gamma-FeOOH) was detected by selected area electron diffraction. It is formed from a double iron Fe(II)/Fe(III) hydroxyl mineral such as 'green rust', or ferrosic hydroxide. Magnetic measurements suggested that lepidocrocite converted to the more stable meaghemite (gamma-Fe203) by mild heat treatment and then to nanophase hematite (aplha-Fe203) by extensive heat treatment. Their chemical reactivity offers a plausible mechanism for the somewhat puzzling observations of the Viking biology experiments. Their unique chemical reactivities are attributed to the combined catalytic effects of the iron oxide/oxyhydroxide and silicate phase surfaces. The mode of formation of these (nanophase) iron oxides on Mars is still unknown.

Strontium isotopes reveal weathering processes in lateritic covers in southern China with implications for paleogeographic reconstructions

Science.gov (United States)

Wei, Xiao; Wang, Shijie; Ji, Hongbing; Shi, Zhenhua

2018-01-01

The isotope ratios of Sr are useful tracers for studying parent material sources, weathering processes, and biogeochemical cycling. Mineralogical and geochemical investigations of two lateritic weathering covers, in an area close to the Tropic of Cancer (Guangxi Province, southern China), were undertaken to study the regional weathering processes and Sr isotopic sources. We found that weathering and decomposition of Rb- and Sr-bearing minerals change the Sr isotopic composition in weathering products (lateritic soils). Weathering of illite lowered the 87Sr/86Sr ratio whereas dissolving and leaching of carbonate minerals increased the 87Sr/86Sr ratio. An Fe nodular horizon is widely developed on the top of the weathering covers in the studied area and it differs from the lateritic soil horizon in mineral composition, construction, and elemental concentration. Furthermore, both Fe2O3 and P2O5 (concentrations) are negatively correlated with the 87Sr/86Sr ratios, suggesting fixation of apatite by Fe oxides is a controlling factor of the Sr isotopic composition in the Fe nodular horizon. The 87Sr/86Sr and Nb/Sr ratios imply the contents and proportions of Fe nodules and clay are critical in controlling the changes of Sr isotopic composition in the Fe nodular horizon. The two stages of the weathering process of carbonate rocks are revealed by the87Sr/86Sr versus Nb/Sr diagram. The 87Sr/86Sr and Rb/Sr ratios suggest that Sr isotopes in the weathering covers within the studied area are derived mainly from parent rock weathering and that the contributions from allothogenic Sr isotopes are limited. A comparison of Sr isotopic composition signatures in the weathering covers of the studied area and Guizhou Province provided insight into the Sr isotopic source and paleogeographic evolution of southern China. From the Permian to the Triassic, the continental fragment sources of the South China sedimentary basin changed significantly. In the Permian, Southern China presented the

Strontium isotopes reveal weathering processes in lateritic covers in southern China with implications for paleogeographic reconstructions.

Directory of Open Access Journals (Sweden)

Xiao Wei

Full Text Available The isotope ratios of Sr are useful tracers for studying parent material sources, weathering processes, and biogeochemical cycling. Mineralogical and geochemical investigations of two lateritic weathering covers, in an area close to the Tropic of Cancer (Guangxi Province, southern China, were undertaken to study the regional weathering processes and Sr isotopic sources. We found that weathering and decomposition of Rb- and Sr-bearing minerals change the Sr isotopic composition in weathering products (lateritic soils. Weathering of illite lowered the 87Sr/86Sr ratio whereas dissolving and leaching of carbonate minerals increased the 87Sr/86Sr ratio. An Fe nodular horizon is widely developed on the top of the weathering covers in the studied area and it differs from the lateritic soil horizon in mineral composition, construction, and elemental concentration. Furthermore, both Fe2O3 and P2O5 (concentrations are negatively correlated with the 87Sr/86Sr ratios, suggesting fixation of apatite by Fe oxides is a controlling factor of the Sr isotopic composition in the Fe nodular horizon. The 87Sr/86Sr and Nb/Sr ratios imply the contents and proportions of Fe nodules and clay are critical in controlling the changes of Sr isotopic composition in the Fe nodular horizon. The two stages of the weathering process of carbonate rocks are revealed by the87Sr/86Sr versus Nb/Sr diagram. The 87Sr/86Sr and Rb/Sr ratios suggest that Sr isotopes in the weathering covers within the studied area are derived mainly from parent rock weathering and that the contributions from allothogenic Sr isotopes are limited. A comparison of Sr isotopic composition signatures in the weathering covers of the studied area and Guizhou Province provided insight into the Sr isotopic source and paleogeographic evolution of southern China. From the Permian to the Triassic, the continental fragment sources of the South China sedimentary basin changed significantly. In the Permian, Southern

Laboratory of minerals purification

International Nuclear Information System (INIS)

2002-01-01

The laboratory of minerals purification was organized in 1962 where with application of modern physical and chemical methods were investigated the mechanism of flotation reagents interaction with minerals' surface, was elaborated technologies on rising complexity of using of republic's minerals

Weather is not significantly correlated with destination-specific transport-related physical activity among adults: A large-scale temporally matched analysis.

Science.gov (United States)

Durand, Casey P; Zhang, Kai; Salvo, Deborah

2017-08-01

Weather is an element of the natural environment that could have a significant effect on physical activity. Existing research, however, indicates only modest correlations between measures of weather and physical activity. This prior work has been limited by a failure to use time-matched weather and physical activity data, or has not adequately examined the different domains of physical activity (transport, leisure, occupational, etc.). Our objective was to identify the correlation between weather variables and destination-specific transport-related physical activity in adults. Data were sourced from the California Household Travel Survey, collected in 2012-3. Weather variables included: relative humidity, temperature, wind speed, and precipitation. Transport-related physical activity (walking) was sourced from participant-recorded travel diaries. Three-part hurdle models were used to analyze the data. Results indicate statistically or substantively insignificant correlations between the weather variables and transport-related physical activity for all destination types. These results provide the strongest evidence to date that transport-related physical activity may occur relatively independently of weather conditions. The knowledge that weather conditions do not seem to be a significant barrier to this domain of activity may potentially expand the universe of geographic locations that are amenable to environmental and programmatic interventions to increase transport-related walking. Copyright © 2017 Elsevier Inc. All rights reserved.

The role of forest trees and their mycorrhizal fungi in carbonate rock weathering and its significance for global carbon cycling.

Science.gov (United States)

Thorley, Rachel M S; Taylor, Lyla L; Banwart, Steve A; Leake, Jonathan R; Beerling, David J

2015-09-01

On million-year timescales, carbonate rock weathering exerts no net effect on atmospheric CO2 concentration. However, on timescales of decades-to-centuries, it can contribute to sequestration of anthropogenic CO2 and increase land-ocean alkalinity flux, counteracting ocean acidification. Historical evidence indicates this flux is sensitive to land use change, and recent experimental evidence suggests that trees and their associated soil microbial communities are major drivers of continental mineral weathering. Here, we review key physical and chemical mechanisms by which the symbiotic mycorrhizal fungi of forest tree roots potentially enhance carbonate rock weathering. Evidence from our ongoing field study at the UK's national pinetum confirms increased weathering of carbonate rocks by a wide range of gymnosperm and angiosperm tree species that form arbuscular (AM) or ectomycorrhizal (EM) fungal partnerships. We demonstrate that calcite-containing rock grains under EM tree species weather significantly faster than those under AM trees, an effect linked to greater soil acidification by EM trees. Weathering and corresponding alkalinity export are likely to increase with rising atmospheric CO2 and associated climate change. Our analyses suggest that strategic planting of fast-growing EM angiosperm taxa on calcite- and dolomite-rich terrain might accelerate the transient sink for atmospheric CO2 and slow rates of ocean acidification. © 2014 The Authors. Plant, Cell & Environment published by John Wiley & Sons Ltd.

Study of arsenopyrite weathering products in mine wastes from abandoned tungsten and tin exploitations

Energy Technology Data Exchange (ETDEWEB)

Murciego, A. [Department of Geology, Plza. de los Caidos s/n. Salamanca University, 37008 Salamanca (Spain); Alvarez-Ayuso, E., E-mail: esther.alvarez@irnasa.csic.es [Department of Environmental Geochemistry, IRNASA (CSIC), Apdo. 257, 37071 Salamanca (Spain); Pellitero, E. [Department of Geology, Plza. de los Caidos s/n. Salamanca University, 37008 Salamanca (Spain); Rodriguez, M.A. [Faculty of Sciences, Crystallography and Mineralogy Area, Avd. Elvas s/n. Extremadura University, 06071 Badajoz (Spain); Garcia-Sanchez, A. [Department of Environmental Geochemistry, IRNASA (CSIC), Apdo. 257, 37071 Salamanca (Spain); Tamayo, A.; Rubio, J.; Rubio, F. [Ceramic and Glass Institute (CSIC), c/Kelsen, 5, 28049 Cantoblanco, Madrid (Spain); Rubin, J. [Material Science Institute of Aragon, CSIC-Zaragoza University, c/Maria de Luna 3, 50009 Zaragoza (Spain)

2011-02-15

Arsenopyrite-rich wastes from abandoned tungsten and tin exploitations were studied to determine the composition and characteristics of the secondary phases formed under natural weathering conditions so as to assess their potential environmental risk. Representative weathered arsenopyrite-bearing rock wastes collected from the mine dumps were analysed using the following techniques: X-ray powder diffraction (XRD) analysis, polarizing microscopy analysis, electron microprobe analysis (EMPA) and microRaman and Moessbauer spectroscopies. Scorodite, pharmacosiderite and amorphous ferric arsenates (AFA) with Fe/As molar ratios in the range 1.2-2.5 were identified as secondary arsenic products. The former showed to be the most abundant and present in the different studied mining areas. Its chemical composition showed to vary in function of the original surrounding rock mineralogy in such a way that phosphoscorodite was found as the mineral variety present in apatite-containing geoenvirons. Other ever-present weathering phases were goethite and hydrous ferric oxides (HFO), displaying, respectively, As retained amounts about 1 and 20% (expressed as As{sub 2}O{sub 5}). The low solubility of scorodite, the relatively low content of AFA and the formation of compounds of variable charge, mostly of amorphous nature, with high capacity to adsorb As attenuate importantly the dispersion of this element into the environment from these arsenopyrite-bearing wastes.

Study of arsenopyrite weathering products in mine wastes from abandoned tungsten and tin exploitations

International Nuclear Information System (INIS)

Murciego, A.; Alvarez-Ayuso, E.; Pellitero, E.; Rodriguez, M.A.; Garcia-Sanchez, A.; Tamayo, A.; Rubio, J.; Rubio, F.; Rubin, J.

2011-01-01

Arsenopyrite-rich wastes from abandoned tungsten and tin exploitations were studied to determine the composition and characteristics of the secondary phases formed under natural weathering conditions so as to assess their potential environmental risk. Representative weathered arsenopyrite-bearing rock wastes collected from the mine dumps were analysed using the following techniques: X-ray powder diffraction (XRD) analysis, polarizing microscopy analysis, electron microprobe analysis (EMPA) and microRaman and Moessbauer spectroscopies. Scorodite, pharmacosiderite and amorphous ferric arsenates (AFA) with Fe/As molar ratios in the range 1.2-2.5 were identified as secondary arsenic products. The former showed to be the most abundant and present in the different studied mining areas. Its chemical composition showed to vary in function of the original surrounding rock mineralogy in such a way that phosphoscorodite was found as the mineral variety present in apatite-containing geoenvirons. Other ever-present weathering phases were goethite and hydrous ferric oxides (HFO), displaying, respectively, As retained amounts about 1 and 20% (expressed as As 2 O 5 ). The low solubility of scorodite, the relatively low content of AFA and the formation of compounds of variable charge, mostly of amorphous nature, with high capacity to adsorb As attenuate importantly the dispersion of this element into the environment from these arsenopyrite-bearing wastes.

Radio nuclides in mineral rocks and beach sand minerals in south east coast, Odisha

International Nuclear Information System (INIS)

Vidya Sagar, D.; Sahoo, S.K.; Essakki, Chinna; Tripathy, S.K.; Ravi, P.M.; Tripathi, R.M.; Mohanty, D.

2014-01-01

The primordial and metamorphic mineral rocks of the Eastern Ghats host minerals such as rutile, ilmenite, Silmenite, zircon, garnet and monazite in quartz matrix. The weathered material is transported down to the sea by run-off through Rivers and deposited back in coastal beach as heavy mineral concentrates. The minerals are mined by M/S Indian Rare Earths Ltd at the Chatrapur plant in Odisha coast to separate the individual minerals. Some of these minerals have low level radioactivity and may pose external and internal radiation hazard. The present paper deals with natural Thorium and Uranium in the source rocks with those observed in the coastal deposits. The study correlates the nuclide activity ratios in environmental samples in an attempt to understand the ecology of the natural radio nuclides of 238 U, 232 Th, 40 K and 226 Ra in environmental context. Further work is in progress to understand the geological process associated with the migration and reconcentration of natural radio-nuclides in the natural high background radiation areas

Mobility of rare earth element in hydrothermal process and weathering product: a review

Science.gov (United States)

Lintjewas, L.; Setiawan, I.

2018-02-01

The Rare Earth Element (REE), consists of La, Ce, Pr, Nd, Pm, Sm, Eu, Gd, Tb, Dy, Lu, Ho, Er, Tm, Yb, are important elements to be used as raw materials of advanced technology such as semiconductors, magnets, and lasers. The research of REE in Indonesia has not been done. Several researches were conducted on granitic rocks and weathering product such as Bangka, Sibolga, West Kalimantan, West Sulawesi and Papua. REE can be formed by hydrothermal processes such as Bayan Obo, South China. The REE study on active hydrothermal system (geothermal) in this case also has the potential to produce mineral deposits. The purpose of this review paper is to know the mobility of REE on hydrothermal process and weathering products. Mobility of REE in the hydrothermal process can change the distribution patterns and REE content such as Ce, Eu, La, Lu, Nd, Sm, and Y. Another process besides the hydrothermal is weathering process. REE mobility is influenced by weathering products, where the REE will experience residual and secondary enrichment processes in heavier minerals.

Physical properties and chemical composition of Segamat Kaolin, Johor, Malaysia

International Nuclear Information System (INIS)

Umar Hamzah; Learn, K.K.; Sahibin Rahim

2010-01-01

Kaolin is a source of secondary mineral as a product of a weathering process of primary minerals. Its main component is fine grain kaolinite (< 2 μm) and it also contains other elements such as aluminium and iron phyllosilicate as the pigment. Aluminium rich kaolin is light in colour with high plasticity and is normally used in the ceramic, plastic, paint, paper, pesticide, pharmacology and cosmetic industries. The physical and chemical characteristics of kaolins are important for its potential application. In this study, about 25 kaolin samples were hand-augered from depths of 1-2 m at Buloh Kasap Segamat, Johor, Malaysia. Chemical analysis carried out included determination of oxides and types of minerals by X-ray diffraction and X-ray fluorescence. Shrinkage rate, rupture modulus and water absorption rate tests were carried out in the physical properties analysis. Plastic and liquid limits of the kaolin were also measured for plastic index. The Segamat kaolin was light in colour due to its high silicate composition. The highest mineral content in the kaolin was kaolinite and quartz occurred as impurities. The low shrinkage rate showed that the kaolin was dense with little voids, hence very suitable for use in the ceramic industry. This kaolin has low water absorption, plasticity and durable according to the rupture modulus test. (author)

Simulation of weathering processes of uranium-nickel ore from Key Lake, Sask., Canada - a contribution of uranium mineralogy to environmental protection

International Nuclear Information System (INIS)

Pechmann, E. von; Voultsidis, V.

1979-01-01

The impact of frost and rain on stockpiles of uranium-nickel or from the Key Lake deposits has been investigated in simulation tests. Frost splitting causes strong disaggregation of the rock and fragmentation of the mineral grains. The ore is much less affected in the sandstone than in the mylonitized basement. During the tests, the uranium minerals have nearly not been weathered. The nickel minerals are quickly transformed into water soluble secondary minerals (sulphates and arsenate). The weathering effects on stored ore depend on the degree of ore comminution and its exposition to the atmospheric elements. (orig.) [de

Chemical composition, antioxidant capacity, and mineral extractability of Sudanese date palm (Phoenix dactylifera L.) fruits

Science.gov (United States)

Mohamed, Rania M A; Fageer, Aisha S M; Eltayeb, Mohamed M; Mohamed Ahmed, Isam A

2014-01-01

The aim of the present work was to investigate the chemical composition, mineral extractability, and antioxidant capacity of six date palm varieties grown in Sudan. The results showed that Sudanese date varieties contained significantly different (P varieties contained significantly varied (P varieties were as follows: ferric-reducing antioxidant power (FRAP) was within the range of 2.82–27.5 mmol/100 g, chelation of Fe2+ ion ranged from 54.31% to 94.98%, and scavenging of H2O2 ranged from 38.48% to 49.13%. There were many correlations (positive, negative, and weak) between antioxidant and mineral extractability of Sudanese date fruits. PMID:25473506

Weathering patinas on the medieval (S. XIV) stained glass windows of the Pedralbes Monastery (Barcelona, Spain).

Science.gov (United States)

Aulinas, Meritxell; Garcia-Valles, Maite; Gimeno, Domingo; Fernandez-Turiel, Jose Luis; Ruggieri, Flavia; Pugès, Montserrat

2009-06-01

moderately weathered stained glass windows, the combination of XRD and FTIR techniques is very useful to obtain a fast preliminary evaluation of the degree of weathering of a stained glass window. The presence of specific mineral phases in the patina (e.g., thenardite) confirms the Na composition of the original stained glass. This is important since Na-rich glass underwent a lesser degree of weathering than K- or K-Ca-rich glass. However, their absence cannot preclude other possibilities. It has been extensively evidenced through time that environmental conditions play an important role on the formation of the different mineral phases which form part of the patinas. The first step in the restoration of a stained glass window is the evaluation of the degree of deterioration of the glass. This evaluation includes a chemical analysis of the glass as well as a characterization of the patinas developed on their surfaces. The obtained results will be essential in order to define the best restoration practices to be followed.

Quantifying Heterogeneities in Soil Cover and Weathering in the Bitterroot and Sapphire Mountains, Montana: Implications for Glacial Legacies and their Morphologic Control on Soil Formation

Science.gov (United States)

Benjaram, S. S.; Dixon, J. L.

2017-12-01

To what extent is chemical weathering governed by a landscape's topography? Quantifying chemical weathering in both steep rocky landscapes and soil-mantled landscapes requires describing heterogeneity in soil and rock cover at local and landscape scales. Two neighboring mountain ranges in the northern Rockies of western Montana, USA, provide an ideal natural laboratory in which to investigate the relationship between soil chemical weathering, persistence of soil cover, and topography. We focus our work in the previously glaciated Bitterroot Mountains, which consist of steep, rock-dominated hillslopes, and the neighboring unglaciated Sapphire Mountains, which display convex, soil-mantled hillslopes. Soil thickness measurements, soil and rock geochemistry, and digital terrain analysis reveal that soils in the rock-dominated Bitterroot Mountains are only slightly less weathered than those in the Sapphire Mountains. However, these differences are magnified when adjusted for rock fragments at a local scale and bedrock cover at a landscape scale, using our newly developed metric, the rock-adjusted chemical depletion fraction (RACDF) and rock-adjusted mass transfer coefficient (RA τ). The Bitterroots overall are 30% less weathered than the Sapphires despite higher mean annual precipitation in the former, with an average rock-adjusted CDF of 0.38 in the postglacial Bitterroots catchment and 0.61 in the nonglacial Sapphire catchment, suggesting that 38% of rock mass is lost in the conversion to soil in the Bitterroots, whereas 61% of rock mass is lost in the nonglaciated Sapphires. Because the previously glaciated Bitterroots are less weathered despite being wetter, we conclude that the glacial history of this landscape exerts more influence on soil chemical weathering than does modern climate. However, while previous studies have correlated weathering intensity with topographic parameters such as slope gradient, we find little topographic indication of specific controls

Profiling contents of water-soluble metabolites and mineral nutrients to evaluate the effects of pesticides and organic and chemical fertilizers on tomato fruit quality.

Science.gov (United States)

Watanabe, Masami; Ohta, Yuko; Licang, Sun; Motoyama, Naoki; Kikuchi, Jun

2015-02-15

In this study, the contents of water-soluble metabolites and mineral nutrients were measured in tomatoes cultured using organic and chemical fertilizers, with or without pesticides. Mineral nutrients and water-soluble metabolites were determined by inductively coupled plasma-atomic emission spectrometry and (1)H nuclear magnetic resonance spectrometry, respectively, and results were analysed by principal components analysis (PCA). The mineral nutrient and water-soluble metabolite profiles differed between organic and chemical fertilizer applications, which accounted for 88.0% and 55.4%, respectively, of the variation. (1)H-(13)C-hetero-nuclear single quantum coherence experiments identified aliphatic protons that contributed to the discrimination of PCA. Pesticide application had little effect on mineral nutrient content (except Fe and P), but affected the correlation between mineral nutrients and metabolites. Differences in the content of mineral nutrients and water-soluble metabolites resulting from different fertilizer and pesticide applications probably affect tomato quality. Copyright © 2014 Elsevier Ltd. All rights reserved.

Exploring Space Weathering on Mercury Using Global UV-VIS Reflectance Spectroscopy

Science.gov (United States)

Izenberg, N. R.; Denevi, B. W.

2018-05-01

We apply UV analysis methods used on lunar LROC data to Mercury to explore space weathering maturity and possibly evidence of shocked minerals. What says the UV // about shock, maturity // on dear Mercury?

Chemical and radiochemical specifications - PWR power plants; Specifications chimiques et radiochimiques - Centrales REP

Energy Technology Data Exchange (ETDEWEB)

Stutzmann, A [Electricite de France (EDF), 93 - Saint-Denis (France)

1997-07-01

Published by EDF this document gives the chemical specifications of the PWR (Pressurized Water Reactor) nuclear power plants. Among the chemical parameters, some have to be respected for the safety. These parameters are listed in the STE (Technical Specifications of Exploitation). The values to respect, the analysis frequencies and the time states of possible drops are noticed in this document with the motion STE under the concerned parameter. (A.L.B.)

Weathering of rock 'Ginger'

Science.gov (United States)

1997-01-01

One of the more unusual rocks at the site is Ginger, located southeast of the lander. Parts of it have the reddest color of any material in view, whereas its rounded lobes are gray and relatively unweathered. These color differences are brought out in the inset, enhanced at the upper right. In the false color image at the lower right, the shape of the visible-wavelength spectrum (related to the abundance of weathered ferric iron minerals) is indicated by the hue of the rocks. Blue indicates relatively unweathered rocks. Typical soils and drift, which are heavily weathered, are shown in green and flesh tones. The very red color in the creases in the rock surface correspond to a crust of ferric minerals. The origin of the rock is uncertain; the ferric crust may have grown underneath the rock, or it may cement pebbles together into a conglomerate. Ginger will be a target of future super-resolution studies to better constrain its origin.Mars Pathfinder is the second in NASA's Discovery program of low-cost spacecraft with highly focused science goals. The Jet Propulsion Laboratory, Pasadena, CA, developed and manages the Mars Pathfinder mission for NASA's Office of Space Science, Washington, D.C. The Imager for Mars Pathfinder (IMP) was developed by the University of Arizona Lunar and Planetary Laboratory under contract to JPL. Peter Smith is the Principal Investigator. JPL is an operating division of the California Institute of Technology (Caltech).

Technical note: Mineralogical, chemical, morphological, and optical interrelationships of mineral dust re-suspensions

Directory of Open Access Journals (Sweden)

J. P. Engelbrecht

2016-08-01

Full Text Available This paper promotes an understanding of the mineralogical, chemical, and physical interrelationships of re-suspended mineral dusts collected as grab samples from global dust sources. Surface soils were collected from arid regions, including the southwestern USA, Mali, Chad, Morocco, Canary Islands, Cabo Verde, Djibouti, Afghanistan, Iraq, Kuwait, Qatar, UAE, Serbia, China, Namibia, Botswana, Australia, and Chile. The  <  38 µm sieved fraction of each sample was re-suspended in a chamber, from which the airborne mineral dust could be extracted, sampled, and analyzed. Instruments integrated into the entrainment facility included two PM10 and two PM2.5 filter samplers, a beta attenuation gauge for the continuous measurement of PM10 and PM2.5 particulate mass fractions, an aerodynamic particle size analyzer, and a three-wavelength (405, 532, 781 nm photoacoustic instrument with integrating reciprocal nephelometer for monitoring absorption and scattering coefficients during the dust re-suspension process. Filter sampling media included Teflon® membrane and quartz fiber filters for chemical analysis and Nuclepore® filters for individual particle analysis by scanning electron microscopy (SEM. The  <  38 µm sieved fractions were also analyzed by X-ray diffraction for their mineral content while the  >  75,  <  125 µm soil fractions were mineralogically assessed by optical microscopy. Presented here are results of the optical measurements, showing the interdependency of single-scattering albedos (SSA at three different wavelengths and mineralogical content of the entrained dust samples. To explain the elevated concentrations of iron (Fe and Fe ∕ Al ratios in the soil re-suspensions, we propose that dust particles are to a large extent composed of nano-sized particles of micas, clays, metal oxides, and ions of potassium (K+, calcium (Ca2+, and sodium (Na+ evenly dispersed as a colloid or adsorbed in amorphous

Room temperature 57Fe Moessbauer spectroscopy of ordinary chondrites from the Atacama Desert (Chile): constraining the weathering processes on desert meteorites

International Nuclear Information System (INIS)

Valenzuela, M.; Abdu, Y.; Scorzelli, R. B.; Duttine, M.; Morata, D.; Munayco, P.

2007-01-01

We report the results of a study on the weathering products of 21 meteorites found in the Atacama Desert (Chile) using room temperature 57 Fe Moessbauer spectroscopy (MS). The meteorites are weathered ordinary chondrites (OCs) with unknown terrestrial ages and include the three chemical groups (H, L, and LL). We obtained the percentage of all the Fe-bearing phases for the primary minerals: olivine, pyroxene, troilite and Fe-Ni metal, and for the ferric alteration products (composed of the paramagnetic Fe 3+ component and the magnetically ordered Fe 3+ components) which gives the percentage of oxidation of the samples. From the Moessbauer absorption areas of these oxides, the terrestrial oxidation of the Atacama OC was found in the range from ∼5% to ∼60%. The amount of silicates as well as the opaques decreases at a constant rate with increasing oxidation level.

A case of the tail wagging the dog? Reverse weathering and Earth's CO2 thermostat.

Science.gov (United States)

Higgins, J. A.

2017-12-01

Feedbacks between climate, the global carbon cycle, and the chemistry of seawater stabilize Earth's surface temperature on geologic timescales and are likely responsible for its habitability over billions of years of Earth history. The most important component of the geologic carbon cycle is the precipitation and burial of carbonate sediments. The amount of carbonate sediment produced depends, in turn, on the alkalinity generated during silicate weathering less the amount consumed during the formation of secondary clay minerals both on the continents and in the ocean. In marine enviroments this process, often referred to as reverse weathering, consumes seawater alkalinity (and cations) via reaction with degraded Al-silicate minerals. Because these reactions constitute a sink of seawater alkalinity, changes in the amount of reverse weathering will lead to imbalances between alkalinity sources and sinks. The net effect is that on timescales greater than the timescale of carbonate compensation (< 10 kyr), changes in reverse weathering will lead to changes in the rate of continental silicate weathering through the dependence of continental silicate weathering on atmospheric CO2 and climate. This mechanism is capable of changing rates of continental silicate weathering without changing either the rate of volcanic outgassing or the rate constant for continental silicate weathering (i.e. through mountain-building or the exposure of different rock types) and as a result represents a unique way of modulating the global carbon cycle and Earth's climate on geologic timescales.

Biologically controlled minerals as potential indicators of life

Science.gov (United States)

Schwartz, D. E.; Mancinelli, R. L.; Kaneshiro, E.

1991-01-01

Minerals can be produced and deposited either by abiotic or biologic means. Regardless of their origin, mineral crystals reflect the environment conditions (e.g., temperature, pressure, chemical composition, and redox potential) present during crystal formation. Biologically-produced mineral crystals are grown or reworked under the control of their host organism and reflect an environment different from the abiotic environment. In addition, minerals of either biologic or abiotic origin have great longevities. For these reasons, biologically produced minerals have been proposed as biomarkers. Biomarkers are key morphological, chemical, and isotopic signatures of living systems that can be used to determine if life processes have occurred. Studies of biologically controlled minerals produced by the protist, Paramecium tetraurelia, were initiated since techniques have already been developed to culture them and isolate their crystalline material, and methods are already in place to analyze this material. Two direct crystalline phases were identified. One phase, whose chemical composition is high in Mg, was identified as struvite. The second phase, whose chemical composition is high in Ca, has not been previously found occurring naturally and may be considered a newly discovered material. Analyses are underway to determine the characteristics of these minerals in order to compare them with characteristics of these minerals in order to compare them with characteristics of minerals formed abiotically, but with the same chemical composition.

Experiments and results of nuclear mineral dressing in Argentina

International Nuclear Information System (INIS)

Mochulsky, M.; Finkesltein, B.; Andres, R.

1992-01-01

This contribution has the purpose to resume the studies and specifics activities of the Physical Processing Division, which deals with the separation of valueless mineral or of those of commercial value, present in Uranium ores. Some general present in Uranium ores. Some general conclusions on the physical techniques of mineral dressing and examples of their application and results obtained by applying several techniques, are shown. The solution of hygroscopicity problems posed by certain chemicals used for the production of potassium fluoro zirconate were also considered. (author)

Complexity of clay mineral formation during 120,000 years of soil development along the Franz Josef chronosequence, New Zealand

International Nuclear Information System (INIS)

Dietel, J.; Dohrmann, R.; Guggenberger, G.; Meyer-Stueve, S.; Turner, S.; Schippers, A.; Kaufhold, S.; Butz-Braun, R.; Condron, L.M.; Mikutta, R.

2017-01-01

Weathering of primary silicates to secondary clay minerals over time affects multiple soil functions such as the accumulation of organic matter and nutrient cations. However, the extent of clay mineral (trans)formation as a function of soil development is poorly understood. In this study, the degree of weathering of sediments along a 120 kyr soil formation gradient was investigated using X-ray diffraction, Fourier transform infrared spectroscopy and X-ray fluorescence spectroscopy. Irrespective of site age, mica and chlorite were the dominant clay minerals. During weathering, a remarkable suite of transitional phases such as vermiculite and several interstratifications with vermiculitic, smectitic, chloritic and micaceous layers developed. The degree of weathering was correlated with soil pH and depletion of K, Ca, Na, Fe and Al, regarding both soil depth and site age. Kaolinite occurred especially at the 120 kyr site, indicating slow formation via transitional phases. The findings of this study revealed that long-term soil development caused complex clay mineral assemblages, both temporally and spatially, and linking this variability to soil functioning warrants further research. (author).

Sorption and Transport of Pharmaceutical chemicals in Organic- and Mineral-rich Soils

Science.gov (United States)

Vulava, V. M.; Schwindaman, J.; Murphey, V.; Kuzma, S.; Cory, W.

2011-12-01

OC, again indicating that these PhACs preferentially partition into the soil OM. Such a correlation was absent for cetirizine. Breakthrough curves of PhACs measured in homogeneous packed soil columns indicated that PhAC transport was affected by chemical nonequilibrium processes depending on the soil and PhAC chemistry. The shape of the breakthrough curves indicated that there were two distinct sorption sites - OM and clay minerals - which influence nonequilibrium transport of these compounds. The retardation factor estimated using the distribution coefficient, Kd, measured from the sorption experiments was very similar to the measured value. While the sorption and transport data do not provide mechanistic information regarding the nature of PhAC interaction with chemical reactive components within geological materials, they do provide important information regarding potential fate of such compounds in the environment. The results also show the role that soil OM and mineral surfaces play in sequestering or transporting these chemicals. These insights have implications to the quality of the water resources in our communities.

Effect of electromagnetic radiation on the physico-chemical properties of minerals; Efecto de la radiacion electromagnetica en las propiedades fisicoquimicas de los minerales

Energy Technology Data Exchange (ETDEWEB)

Lopez M, A.; Delgadillo G, J. A. [Universidad Autonoma de San Luis Potosi, Instituto de Metalurgia, Doctorado Institucional de Ingenieria y Ciencia de Materiales, Av. Sierra Leona 550, 78210 San Luis Potosi (Mexico); Vega C, H. R., E-mail: alopezm6@yahoo.com.mx [Universidad Autonoma de Zacatecas, Unidad Academica de Estudios Nucleares, Cipres No. 10, Fracc. La Penuela, 98068 Zacatecas (Mexico)

2014-08-15

The electromagnetic radiation effect represented by gamma rays was investigated through; chemical analysis, X-ray diffraction (XRD), scanning electron microscopy (Sem) and magnetization when applied at a dose of 0.5704 Gy (0.5704 J/ kg) at a feed relation of 18.40 ± 1.13 mGy/ h., in different minerals; in order to characterize the impact of the same from {sup 137}Cs in the physicochemical properties of these minerals. All the irradiated samples showed chemical stability at this stage undetectable other both in the XRD study and in the images analysis obtained by Sem; and at present almost the same chemical composition as the non-irradiated samples. So the same patterns of X-ray diffraction thereof, show a tendency to slightly lower the intensity of the most representative peaks of each mineral phase, which may be due to a decrease in crystallinity or preferential crystallographic orientation in crystals. In the micrographs analysis obtained by Sem on the irradiated samples, some holes (open pores) present in the particles were observed, mainly chalcopyrite and sphalerite lesser extent, seen this fact may be due to Compton Effect, in the radiation process. In relation to the magnetization property, a variation is obtained in the saturation magnetization (Ms) for the irradiated samples containing iron and more significantly in the chalcopyrite case. Therefore, with the radiation level used; slight changes occurring in the physical properties of minerals, whereas they remained stable chemically. These small changes may represent a signal that electromagnetic radiation applied at higher doses, is a viable option for improving the mineral processing. (author)

Dual-functioning peptides discovered by phage display increase the magnitude and specificity of BMSC attachment to mineralized biomaterials.

Science.gov (United States)

Ramaraju, Harsha; Miller, Sharon J; Kohn, David H

2017-07-01

Design of biomaterials for cell-based therapies requires presentation of specific physical and chemical cues to cells, analogous to cues provided by native extracellular matrices (ECM). We previously identified a peptide sequence with high affinity towards apatite (VTKHLNQISQSY, VTK) using phage display. The aims of this study were to identify a human MSC-specific peptide sequence through phage display, combine it with the apatite-specific sequence, and verify the specificity of the combined dual-functioning peptide to both apatite and human bone marrow stromal cells. In this study, a combinatorial phage display identified the cell binding sequence (DPIYALSWSGMA, DPI) which was combined with the mineral binding sequence to generate the dual peptide DPI-VTK. DPI-VTK demonstrated significantly greater binding affinity (1/K D ) to apatite surfaces compared to VTK, phosphorylated VTK (VTK phos ), DPI-VTK phos , RGD-VTK, and peptide-free apatite surfaces (p biomaterial surfaces and subsequently increase cell proliferation and differentiation. These new peptides expand biomaterial design methodology for cell-based regeneration of bone defects. This strategy of combining cell and material binding phage display derived peptides is broadly applicable to a variety of systems requiring targeted adhesion of specific cell populations, and may be generalized to the engineering of any adhesion surface. Copyright © 2017 Elsevier Ltd. All rights reserved.

New Au-U deposit type in the weathering crust in tectonicmetasomatite zones of Pre-Cambrian shields

International Nuclear Information System (INIS)

Tarkhanov, A.

2014-01-01

Au-U mineralization is widely distributed in the tectonic-metasomatite zones of Pre-Cambrian shields (Aldan Shield, Ukraine Shield and others). The industrial ores are located only in several areas at depths of more than 150-300 m. Uranium mineralization is represented by uranotitnates and the gold mineralization by auriferous pyrite. The zone of weathering is present to the depth of 100-150 m. The feldspars are replaced by the clay minerals, carbonates are dissovled, sulfides are oxidized and the secondary minerals of uranium replace uranotitanates.The golden mineralization in the envelope of weathering is represented by the fine-grained native gold. The particle size is 40-50 nm. Uranium mineralization is in the form of relict brannerite, tuyamunite, torbernite, carnotite. The gold content is 1-2 g/t, and uranium content 0.01- 0.05% U. Ore bodies of gold and uranium are located inside the tectonic-metasomatite zones. The zones of maximum concentration of these metals may not coincide. The gold ore bodies have the length of hundreds meters and a thickness of 1-5 m. The vertical extent of the secondary Au-U mineralization is 100-150 m. 20 laboratory samples of ore from the weathered zone were tested by the method of heap leaching. The first stage is the uranium leach by diluted sulfuric acid. The second stage is the cyanation of gold and silver. The experimental data indicates leach rate of uranium 75%, gold 80-97%, silver 50-60%. Gold resources in the continous zone is estimated to be 80 t. Gold resources of the several other zones inside the area of 100 km 2 are estimated as 220 t. The heap leach process can be used for profitable development of the low-grade deposits. This method helps to increase the resources of gold and uranium. (author)

Post-precipitation bias in band-tailed pigeon surveys conducted at mineral sites

Science.gov (United States)

Overton, C.T.; Schmitz, R.A.; Casazza, Michael L.

2005-01-01

Many animal surveys to estimate populations or index trends include protocol prohibiting counts during rain but fail to address effects of rainfall preceding the count. Prior research on Pacific Coast band-tailed pigeons (Patagioenas fasciata monilis) documented declines in use of mineral sites during rainfall. We hypothesized that prior precipitation was associated with a short-term increase in use of mineral sites following rain. We conducted weekly counts of band-tailed pigeons at 19 Pacific Northwest mineral sites in 2001 and 20 sites in 2002. Results from regression analysis indicated higher counts ???2 days after rain (11.31??5.00% [x????SE]) compared to ???3 days. Individual index counts conducted ???2 days after rain were biased high, resulting in reduced ability to accurately estimate population trends. Models of band-tailed pigeon visitation rates throughout the summer showed increased mineral-site counts during both June and August migration periods, relative to the July breeding period. Our research supported previous studies recommending that mineral-site counts used to index the band-tailed pigeon population be conducted during July. We further recommend conducting counts >3 days after rain to avoid weather-related bias in index estimation. The design of other population sampling strategies that rely on annual counts should consider the influence of aberrant weather not only coincident with but also preceding surveys if weather patterns are thought to influence behavior or detection probability of target species.

Structural control of weathering processes within exhumed granitoids: Compartmentalisation of geophysical properties by faults and fractures

Science.gov (United States)

Place, J.; Géraud, Y.; Diraison, M.; Herquel, G.; Edel, J.-B.; Bano, M.; Le Garzic, E.; Walter, B.

2016-03-01

In the latter stages of exhumation processes, rocks undergo weathering. Weathering halos have been described in the vicinity of structures such as faults, veins or dykes, with a lateral size gradually narrowing with depth, symmetrically around the structures. In this paper, we describe the geophysical characterisation of such alteration patterns on two granitoid outcrops of the Catalan Coastal Ranges (Spain), each of which is affected by one major fault, as well as minor faults and fractures. Seismic, electric and ground penetrating radar surveys were carried out to map the spatial distribution of P-wave velocity, electrical resistivity and to identify reflectors of electromagnetic waves. The analysis of this multi-method and complementary dataset revealed that, at shallow depth, geophysical properties of the materials are compartmentalised and asymmetric with respect to major and subsidiary faults affecting the rock mass. This compartmentalisation and asymmetry both tend to attenuate with depth, whereas the effect of weathering is more symmetric with respect to the major structure of the outcrops. We interpret such compartmentalisation as resulting from the role of hydraulic and mechanical boundaries played by subsidiary faults, which tend to govern both the chemical and physical alterations involved in weathering. Thus, the smoothly narrowing halo model is not always accurate, as weathering halos can be strongly asymmetrical and present highly irregular contours delimiting sharp contrasts of geophysical properties. These results should be considered when investigating and modelling fluid storage and transfer in top crystalline rock settings for groundwater applications, hydrocarbon or geothermal reservoirs, as well as mineral deposits.

Chemical characteristics and mineral composition of quinoa by near-infrared spectroscopy.

Science.gov (United States)

González Martín, M Inmaculada; Wells Moncada, Guillermo; Fischer, Susana; Escuredo, Olga

2014-03-30

Quinoa (Chenopodium quinoa Willd.) has been traditionally used as a foodstuff in the Andes and it has gained increasing interest in recent years owing to its high nutritional value. The potential of near-infrared spectroscopy (NIRS) for estimating chemical compounds in quinoa was studied because of the possibility of conducting direct measurement without prior sample treatment. The use of NIRS technology with a remote reflectance fiber-optic probe for the analysis of major compounds and mineral composition of 48 quinoa samples was studied. The calibration of the NIRS instrument was conducted using modified partial least squares (MPLS) analysis. This allowed the determination of protein (16.0-20.2 g 100g⁻¹), crude fiber (1.8-3.1 g 100g⁻¹), fat (4.4-7.5 g 100g⁻¹), calcium (298.8-1164.5 mg kg⁻¹), iron (0-948.5 mg kg⁻¹) and phosphorus (2735.0-4543.3 mg kg⁻¹). The correlation coefficients (RSQ) were 0.83 for protein, 0.73 for crude fiber, 0.93 for fat; 0.60 for calcium; 0.76 for iron and 0.75 for phosphorus. The robustness of the equations obtained was verified by external validation on unknown quinoa samples. NIRS with fiber-optic probe provides an alternative for the determination of chemical compounds of quinoa, faster and at lower cost, with results comparable with chemical methods. © 2013 Society of Chemical Industry.

Impact of Poultry Litter Cake, Cleanout, and Bedding following Chemical Amendments on Soil C and N Mineralization

OpenAIRE

Watts, Dexter B.; Smith, Katy E.; Torbert, H. A.

2012-01-01

Poultry litter is a great alternative N source for crop production. However, recent poultry litter management changes, and increased chemical amendment use may impact its N availability. Thus, research was initiated to evaluate the effect that broiler cake and total cleanout litter amended with chemical additives have on C and N mineralization. A 35-day incubation study was carried out on a Hartsells fine sandy loam (fine-loamy, siliceous, subactive, thermic Typic Hapludults) soil common to t...

Geochemical interpretation of the Precambrian basement and overlying Cambrian sandstone on Bornholm, Denmark: Implications for the weathering history

Science.gov (United States)

Zhou, Lingli; Friis, Henrik; Yang, Tian; Nielsen, Arne Thorshøj

2017-08-01

A geochemical study of the Precambrian basement granites from the Borggård borehole on Bornholm, Denmark, suggests that the granites were moderately weathered (Chemical Index of Alteration-CIA = 66-71) during subaerial exposure in a humid climate. The microcline is well preserved, whereas plagioclase was thoroughly altered to clay minerals (Plagioclase Index of Alteration-PIA = 93-99) which is likely due to its original Ca-rich composition. The primary Fe-Ti accessory minerals were oxidized to hematite and anatase. Evidence from REE distribution patterns and immobile element ratios, e.g. Zr/Hf and Nb/Ta, between the weathered basement granite from the Borggård borehole and regional granitoids on Bornholm, constrains the Svaneke Granite as the original basement lithology. A tau (τ) mass transport model (assuming immobile Ti) was applied to quantify the mass transfer during weathering of the basement granite. The results show a depletion of major elements in the following order: Na > Ca > Mg > Si; Al and Ti are immobile and stay constant; K shows sample dependent enrichment or depletion; Fe is slightly enriched. The Cambrian sandstone overlying the basement in the Borggård borehole, assigned to the Gadeby Member of the Nexø Formation, is feldspathic litharenite-litharenite in composition. Provenance indicators including (Gd/Yb)N, Zr/Hf and Nb/Ta ratios and petrological features indicate that source material was derived from both weathered and fresh basement granite of intermediate composition. The Gadeby Member equivalents in Germany, the basal lower Cambrian Adlergrund Konglomerat Member (AKM) in the offshore G-14 well north of Rügen, and the approximately coeval Lubmin Sandstein Formation (LSF) from the Loissin-1 borehole, mainland Germany, must have been sourced from a basement with compositions comparable to the intermediate group of the regional granitoids on Bornholm. The source materials for the AKM (CIA = 71-72, PIA = 94-96), the Gadeby Member in the

Questa Baseline and Pre-mining Ground-Water Quality Investigation, 7. A Pictorial Record of Chemical Weathering, Erosional Processes, and Potential Debris-flow Hazards in Scar Areas Developed on Hydrothermally Altered Rocks

Science.gov (United States)

Plumlee, Geoffrey S.; Ludington, Steve; Vincent, Kirk R.; Verplanck, Philip L.; Caine, Jonathan S.; Livo, K. Eric

2009-01-01

Erosional scar areas developed along the lower Red River basin, New Mexico, reveal a complex natural history of mineralizing processes, rapid chemical weathering, and intense physical erosion during periodic outbursts of destructive, storm-induced runoff events. The scar areas are prominent erosional features with craggy headwalls and steep, denuded slopes. The largest scar areas, including, from east to west, Hottentot Creek, Straight Creek, Hansen Creek, Lower Hansen Creek, Sulfur Gulch, and Goat Hill Gulch, head along high east-west trending ridges that form the northern and southern boundaries of the lower Red River basin. Smaller, topographically lower scar areas are developed on ridge noses in the inner Red River valley. Several of the natural scar areas have been modified substantially as a result of large-scale open-pit and underground mining at the Questa Mine; for example, much of the Sulfur Gulch scar was removed by open pit mining, and several scars are now partially or completely covered by mine waste dumps.

Thermo-mineral waters of Hammam Meskoutine (north-east Algeria: Composition and origin of mineralization

Directory of Open Access Journals (Sweden)

Benamara Abdelwaheb

2017-09-01

Full Text Available The extreme north-eastern Algeria, in particular the Guelma city conceals thermal springs, whose waters circulating at great depths allow the rain-waters to warm up (according to the average geothermal gradient of 1°C per 33 m and to acquire a mineralization which depends on the traversed rock. The goal of this research work was to determine mineralization origin of the thermo-mineral waters of Hammam Meskoutine (Algerian N-E. A hydro-chemical study involved analyses of a number of physical and chemical parameters of waters such as: temperature, hydrogen potential, electrolytical conductivity, Cl-, SO4 2-, HCO3 -, Ca2+, Mg2+, K+ and Na+. The data processing on the diagram revealed two dominating chemical facies: sulphate-magnesium and bicarbonate magnesium. With a high conductivity in excess of 2300 μS·cm-1, the temperature reaches 97°C. Calculation of the saturation index shows that the waters are supersaturated in carbonate minerals (calcite, dolomite and aragonite and less saturated with evaporite minerals (halite, anhydrite, sylvite and gypsum. The reconstitution in dissolved salts reveals a dominant salt rich in calcium bicarbonates, in calcium sulphates and secondarily in magnesium salts. Geological sections used in the study zone affirm that the chemical composition of the spring waters comes from the neritic limestone dissolution and the gypso-saline complex of Hammam Meskoutine.

Selective intake of potassium from K-bearing silicate minerals by sunflower and upland rice inferred from Eu anomaly. Implication for weathering as a direct consequence of plant physiology

International Nuclear Information System (INIS)

Akagi, Tasuku; Saito, Sakura; Watanabe, Shin-ichi; Sugiyama, Megumi; Ae, Noriharu

2006-01-01

Two crops (sunflower and upland rice) cultivated using three K-bearing minerals and KCl by Sugiyama and Ae (2000) were analyzed for rare earth elements (REEs). The two crops had been reported by them to general more available silica in soil (especially in the case of sunflower) and absorbed silica in plants (especially in the case of upland rice) than that available originally in soil. The K-bearing minerals included biotite, muscovite, and K-feldspar. The REE patterns of individual crop specimens exhibited different extents of Eu anomaly; upland rice exhibited more varying extent of Eu anomaly than sunflower. It is inferred that REEs released from the K-bearing minerals had a longer contact with soil in the case of sunflower than in the case of upland rice. By the scrutiny of the extent of the Eu anomaly, it was found that upland rice took in K and REEs from all the K-bearing minerals, including hardly-soluble feldspar. Eu anomaly can be a good proxy of sources of inorganic nutrients in plants as well as of the directness of absorption of the nutrients. When the present results are viewed from a different angle, they endorse that plant-induced weathering is equivalent to physiological action of plants. (author)

Weathering processes and the composition of inorganic material transported through the orinoco river system, Venezuela and Colombia

Science.gov (United States)

Stallard, R.F.; Koehnken, L.; Johnsson, M.J.

1991-01-01

The composition of river-borne material in the Orinoco River system is related primarily to erosion regime, which in turn is related to tectonic setting; especially notable is the contrast between material derived from tectonically active mountain belts and that from stable cratonic regions. For a particular morpho-tectonic region, the compositional suites of suspended sediment, bed material, overback deposits, and dissolved phases are fairly uniform are are typically distinct from whose of other regions. For each region, a consistent set of chemical weathering reactions can be formulated to explain the composition of dissolved and solid loads. In developing these formulations, erosion on slopes and storage of solids in soils and alluvial sediments are important considerations. Compositionally verymature sediment is derived from areas of thick soils where erosion is transport limited and from areas where sediments are stored for extended periods of time in alluvial deposits. Compositionally immature sediments are derived from tectonically active mountain belts where erosion is weathering limited. Weathering-limited erosion also is important in the elevated parts of the Guayana Shield within areas of sleep topography. Compared to the mountain belts, sediments derived from elevated parts of the Shield are more mature. A greater degree of chemical weathering seems to be needed to erode the rock types typical of the Shield. The major-element chemistry and mineral composition of sediment delivered by the Orinoco River to the ocean are controlled by rivers that have their headwaters in mountain belts and cross the Llanos, a region of alluvial plains within the foreland basin. The composition of sediments in rivers that drain the Shield seems to be established primarily at the site of soil formation, whereas for rivers that drain the mountain belts, additional weathering occurs during s episodes of storage on alluvial plains as sediments are transported across the Llanos

Trace-element analysis of Antarctic H chondrites: Chemical weathering and comparisons with their non-Antarctic counterparts

International Nuclear Information System (INIS)

Kwok, J.E.

1986-01-01

Large numbers of meteorites have been discovered in Antarctica over the last decade (7000 fragments probably representing over 1200 separate events). They are important for their numbers and for their complement of unique or rare specimens; they also have long terrestrial ages (up to 1,000,000 years) compared to non-Antarctic falls (usually < 200 years). We report compositional data for mobile/volatile trace elements Ag, Au, Bi, Cd, Co, Cs, In, Rb, Sb, Se, Te, Ti, U, and Zn in a suite of Antarctic H chondrites. Our data show that heavily oxidized H chondrites are leached of a portion of their trace elements and, therefore, have been chemically compromised by their stay in Antarctica. The less oxidized specimens seem to have retained their chemical integrity. We suggest possibilities for using chemical data to measure the degree of a chondrite's chemical weathering. We compare our data to that obtained previously for non-Antarctic H chondrites (Linger et al., 1986), by petrologic type (H4, H5, H6, H4-6) and shock-loading (moderately shocked facies a-c, heavily shocked facies d-f). Many statistically significant differences are found between non-Antarctic and Victoria Land, Antarctica H chondrites of each petrologic type and of shock facies d-f

Uranium Release from Acidic Weathered Hanford Sediments: Single-Pass Flow-Through and Column Experiments.

Science.gov (United States)

Wang, Guohui; Um, Wooyong; Wang, Zheming; Reinoso-Maset, Estela; Washton, Nancy M; Mueller, Karl T; Perdrial, Nicolas; O'Day, Peggy A; Chorover, Jon

2017-10-03

The reaction of acidic radioactive waste with sediments can induce mineral transformation reactions that, in turn, control contaminant fate. Here, sediment weathering by synthetic uranium-containing acid solutions was investigated using bench-scale experiments to simulate waste disposal conditions at Hanford's cribs (Hanford, WA). During acid weathering, the presence of phosphate exerted a strong influence over uranium mineralogy and a rapidly precipitated, crystalline uranium phosphate phase (meta-ankoleite [K(UO 2 )(PO 4 )·3H 2 O]) was identified using spectroscopic and diffraction-based techniques. In phosphate-free system, uranium oxyhydroxide minerals such as K-compreignacite [K 2 (UO 2 ) 6 O 4 (OH) 6 ·7H 2 O] were formed. Single-pass flow-through (SPFT) and column leaching experiments using synthetic Hanford pore water showed that uranium precipitated as meta-ankoleite during acid weathering was strongly retained in the sediments, with an average release rate of 2.67 × 10 -12 mol g -1 s -1 . In the absence of phosphate, uranium release was controlled by dissolution of uranium oxyhydroxide (compreignacite-type) mineral with a release rate of 1.05-2.42 × 10 -10 mol g -1 s -1 . The uranium mineralogy and release rates determined for both systems in this study support the development of accurate U-release models for the prediction of contaminant transport. These results suggest that phosphate minerals may be a good candidate for uranium remediation approaches at contaminated sites.

Uranium Release from Acidic Weathered Hanford Sediments: Single-Pass Flow-Through and Column Experiments

Energy Technology Data Exchange (ETDEWEB)

Wang, Guohui [Pacific Northwest National Laboratory, Richland, Washington 99354, United States; Um, Wooyong [Pacific Northwest National Laboratory, Richland, Washington 99354, United States; Pohang University of Science and Technology (POSTECH), Pohang, South Korea; Wang, Zheming [Pacific Northwest National Laboratory, Richland, Washington 99354, United States; Reinoso-Maset, Estela [Sierra; Washton, Nancy M. [Pacific Northwest National Laboratory, Richland, Washington 99354, United States; Mueller, Karl T. [Pacific Northwest National Laboratory, Richland, Washington 99354, United States; Perdrial, Nicolas [Department; Department; O’Day, Peggy A. [Sierra; Chorover, Jon [Department

2017-09-21

The reaction of acidic radioactive waste with sediments can induce mineral transformation reactions that, in turn, control contaminant fate. Here, sediment weathering by synthetic uranium-containing acid solutions was investigated using bench-scale experiments to simulate waste disposal conditions at Hanford’s cribs, USA. During acid weathering, the presence of phosphate exerted a strong influence over uranium mineralogy and a rapidly precipitated, crystalline uranium phosphate phase (meta-ankoleite [K(UO2)(PO4)·3H2O]) was identified using spectroscopic and diffraction-based techniques. In phosphate-free system, uranium oxyhydroxide minerals such as K-compreignacite [K2(UO2)6O4(OH)6·7H2O] were formed. Single-pass flow-through (SPFT) and column leaching experiments using synthetic Hanford pore water showed that uranium precipitated as meta-ankoleite during acid weathering was strongly retained in the sediments, with an average release rate of 2.67E-12 mol g-1 s-1. In the absence of phosphate, uranium release was controlled by dissolution of uranium oxyhydroxide (compreignacite-type) mineral with a release rate of 1.05-2.42E-10 mol g-1 s-1. The uranium mineralogy and release rates determined for both systems in this study support the development of accurate U-release models for prediction of contaminant transport. These results suggest that phosphate minerals may be a good candidate for uranium remediation approaches at contaminated sites.

How biological crusts are stabilizing the soil surface? The devolpment of organo-mineral interactions in the initial phase

Science.gov (United States)

Fischer, T.; Veste, M.; Wiehe, W.; Lange, P.

2009-04-01

First colonizers of new land surfaces are cryptogames which often form biological soil crusts (BSC) covering the first millimetre of the top soil in many ecosystems from polar to desert ecosystems. These BSC are assemblages of cyanobacteria, green algae, mosses, liverworts, fungi and/or lichens. The development of soil surface crusts plays a major role for the further vegetation pattern through changes to the physico-chemical conditions and influencing various ecosystem processes. We studied the development of BSC on quaternary substrate of an initial artificial water catchment in Lusatia, Germany. Due to lack of organic matter in the geological substrate, photoautotrophic organisms like green algae and cyanobacteria dominated the initial phases of ecosystem development and, hence, of organo-mineral ineractions. We combined SEM/EDX and FTIR microscopy to study the contact zone of extracellular polymeric substances (EPS) of green algae and cyanobacteria with quartz, spars and mica on a >40 µm scale in undisturbed biological soil crusts, which had a maximum thickness of approx. 2 mm. SEM/EDX microscopy was used to determine the spatial distribution of S, Ca, Fe, Al, Si and K in the profiles, organic compounds were identified using FTIR microscopy. Exudates of crust organisms served as cementing material between sand particles. The crust could be subdivided into two horizontal layers. The upper layer, which had a thickness of approx. 200 µm, is characterized by accumulation of Al and K, but absence of Fe in microbial derived organic matter, indicating capture of weathering products of feldspars and mica by microbial exudates. The pore space between mineral particles was entirely filled with organic matter here. The underlying layer can be characterized by empty pores and organo-mineral bridges between the sand particles. Contrarily to the upper layer of the crust, Fe, Al and Si were associated with organic matter here but K was absent. Highest similarity of the FTIR

NASA Aviation Safety Program Weather Accident Prevention/weather Information Communications (WINCOMM)

Science.gov (United States)

Feinberg, Arthur; Tauss, James; Chomos, Gerald (Technical Monitor)

2002-01-01

Weather is a contributing factor in approximately 25-30 percent of general aviation accidents. The lack of timely, accurate and usable weather information to the general aviation pilot in the cockpit to enhance pilot situational awareness and improve pilot judgment remains a major impediment to improving aviation safety. NASA Glenn Research Center commissioned this 120 day weather datalink market survey to assess the technologies, infrastructure, products, and services of commercial avionics systems being marketed to the general aviation community to address these longstanding safety concerns. A market survey of companies providing or proposing to provide graphical weather information to the general aviation cockpit was conducted. Fifteen commercial companies were surveyed. These systems are characterized and evaluated in this report by availability, end-user pricing/cost, system constraints/limits and technical specifications. An analysis of market survey results and an evaluation of product offerings were made. In addition, recommendations to NASA for additional research and technology development investment have been made as a result of this survey to accelerate deployment of cockpit weather information systems for enhancing aviation safety.

Weather Augmented Risk Determination (WARD) System

Science.gov (United States)

Niknejad, M.; Mazdiyasni, O.; Momtaz, F.; AghaKouchak, A.

2017-12-01

Extreme climatic events have direct and indirect impacts on society, economy and the environment. Based on the United States Bureau of Economic Analysis (BEA) data, over one third of the U.S. GDP can be considered as weather-sensitive involving some degree of weather risk. This expands from a local scale concrete foundation construction to large scale transportation systems. Extreme and unexpected weather conditions have always been considered as one of the probable risks to human health, productivity and activities. The construction industry is a large sector of the economy, and is also greatly influenced by weather-related risks including work stoppage and low labor productivity. Identification and quantification of these risks, and providing mitigation of their effects are always the concerns of construction project managers. In addition to severe weather conditions' destructive effects, seasonal changes in weather conditions can also have negative impacts on human health. Work stoppage and reduced labor productivity can be caused by precipitation, wind, temperature, relative humidity and other weather conditions. Historical and project-specific weather information can improve better project management and mitigation planning, and ultimately reduce the risk of weather-related conditions. This paper proposes new software for project-specific user-defined data analysis that offers (a) probability of work stoppage and the estimated project length considering weather conditions; (b) information on reduced labor productivity and its impacts on project duration; and (c) probabilistic information on the project timeline based on both weather-related work stoppage and labor productivity. The software (WARD System) is designed such that it can be integrated into the already available project management tools. While the system and presented application focuses on the construction industry, the developed software is general and can be used for any application that involves

A microbial-mineralization approach for syntheses of iron oxides with a high specific surface area.

Science.gov (United States)

Yagita, Naoki; Oaki, Yuya; Imai, Hiroaki

2013-04-02

Of minerals and microbes: A microbial-mineralization-inspired approach was used to facilitate the syntheses of iron oxides with a high specific surface area, such as 253 m(2)g(-1) for maghemite (γ-Fe(2)O(3)) and 148 m(2)g(-1) for hematite (α-Fe(2)O(3)). These iron oxides can be applied to electrode material of lithium-ion batteries, adsorbents, and catalysts. Copyright © 2013 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

The greenhouse effect and extreme weather

International Nuclear Information System (INIS)

Groenaas, Sigbjoern; Kvamstoe, Nils Gunnar

2002-01-01

The article asserts that an anthropogenic global warming is occurring. This greenhouse effect is expected to cause more occurrences of extreme weather. It is extremely difficult, however, to relate specific weather catastrophes to global warming with certainty, since such extreme weather conditions are rare historically. The subject is controversial. The article also discusses the public debate and the risk of floods

30 CFR 48.26 - Experienced miner training.

Science.gov (United States)

2010-07-01

... the physical and health hazards of chemicals in the miner's work area, the protective measures a miner... occurred during the miner's absence and that could adversely affect the miner's health or safety. (1) A... Mineral Resources MINE SAFETY AND HEALTH ADMINISTRATION, DEPARTMENT OF LABOR EDUCATION AND TRAINING...

Glacial alteration of volcanic terrains: A chemical investigation of the Three Sisters, Oregon, USA.

Science.gov (United States)

Rutledge, Alicia; Horgan, Briony; Havig, Jeff

2017-04-01

Glacial silica cycling is more efficient than previously reported, and in some settings, particularly glaciated mafic volcanics, can be the dominant weathering process. Based on field work at glaciated volcanic sites, we hypothesize that this is due to a combination of high rates of silica dissolution from mafic bedrock and reprecipitation of silica in the form of opaline silica coatings and other poorly crystalline silicate alteration phases. The high rate of bedrock comminution in subglacial environments results in high rates of both chemical and physical weathering, due to the increased reactive mineral surface area formed through glacial grinding. In most bedrock types, carbonate weathering is enhanced and silica fluxes are depressed in glacial outwash compared with global average riverine catchment runoff due to low temperatures and short residence times. However, in mafic systems, higher dissolved SiO2 concentrations have been observed. The major difference between observed glacial alteration of volcanic bedrock and more typical continental terrains is the absence of significant dissolved carbonate in the former. In the absence of carbonate minerals which normally dominate dissolution processes at glacier beds, carbonation of feldspar can become the dominant weathering process, which can result in a high proportion of dissolved silica fluxes in glacial outwash waters compared to the total cation flux. Mafic volcanic rocks are particularly susceptible to silica mobility, due to the high concentration of soluble minerals (i.e. plagioclase) as compared to the high concentration of insoluble quartz found in felsic rocks. To investigate melt-driven chemical weathering of mafic volcanics, water and rock samples were collected during July 2016 from glaciated volcanic bedrock in the Three Sisters Wilderness, Oregon, U.S.A. (44°9'N, 121°46'W): Collier Glacier (basaltic andesite, andesite), Hayden Glacier (andesite, dacite), and Diller Glacier (basalt). Here we

TUCS/phosphate mineralization of actinides

Energy Technology Data Exchange (ETDEWEB)

Nash, K.L. [Argonne National Lab., IL (United States)

1997-10-01

This program has as its objective the development of a new technology that combines cation exchange and mineralization to reduce the concentration of heavy metals (in particular actinides) in groundwaters. The treatment regimen must be compatible with the groundwater and soil, potentially using groundwater/soil components to aid in the immobilization process. The delivery system (probably a water-soluble chelating agent) should first concentrate the radionuclides then release the precipitating anion, which forms thermodynamically stable mineral phases, either with the target metal ions alone or in combination with matrix cations. This approach should generate thermodynamically stable mineral phases resistant to weathering. The chelating agent should decompose spontaneously with time, release the mineralizing agent, and leave a residue that does not interfere with mineral formation. For the actinides, the ideal compound probably will release phosphate, as actinide phosphate mineral phases are among the least soluble species for these metals. The most promising means of delivering the precipitant would be to use a water-soluble, hydrolytically unstable complexant that functions in the initial stages as a cation exchanger to concentrate the metal ions. As it decomposes, the chelating agent releases phosphate to foster formation of crystalline mineral phases. Because it involves only the application of inexpensive reagents, the method of phosphate mineralization promises to be an economical alternative for in situ immobilization of radionuclides (actinides in particular). The method relies on the inherent (thermodynamic) stability of actinide mineral phases.

Experimental study of the uranium mobility due to the weathering action at the uraniferous district of Caetite/Lagoa Real, Bahia, Brazil

International Nuclear Information System (INIS)

Scislewski, Alexandro Rocha

2004-01-01

In the present research, the proposal was to develop a preliminary study about the geochemical behavior of determined chemical elements, mainly the uranium, during the action of weathering processes in the rocks that bear the uranium mineralizations of the Caetite-Lagoa Real region, State of Bahia, more specifically of the Jazida Cachoeira uranium mine. To reach this purpose were used samples that represent several stages of the milling process of the uranium ore, so selecting representatives of the host rock, the ore and the treated ore (waste from the milling plant) to be used in the laboratory-controlled experiments. The samples were dried, sieved and finally introduced in the reactors, these adapted from the Flow-Through Reactor of Brantley and Chen. In the geochemical point of view, the results of the experiments showed a distinct behavior between the samples. It was observed that the treated ore, in relation to the host rocks of the ore and the own ore, shown a faster and homogeneous interaction with the leaching solution; it was also noted that in the output solution of the treated ore samples existed a significant complexation of the uranium by the sulfate (S0 4 -2 ), ), instead of the non treated samples (host rock and ore) that were complexed mainly by the carbonate (C0 3 -2 ). These different results are attributed to the alterations imposed to the rock during the milling process, and occur mainly, during the acid attack in the leaching process of the milling plant. The results and conclusions of this research, in spite of been preliminary, are essential to understand the behavior of the geochemical speciation of the effluent solutions; to understand the alterations of a rock matrix, and finally, to understand the migration chemical behavior of the related chemical elements. It is expected that these results contribute, in the future, to a deeper knowledge of the processes that control the chemical composition of the natural waters from this region in

Weathering of plagioclase across variable flow and solute transport regimes

NARCIS (Netherlands)

Pacheco, F.A.L.; Weijden, C.H. van der

2012-01-01

The study area is situated in a fault zone with fractured granites and metasediments. In a conceptual model, infiltrating water first passes the bedrock cover of soil and saprolite and then partly enters the fractures. Weathering reactions of minerals occur in small pores and fissures in the bedrock

On nutrients and trace metals: Effects from Enhanced Weathering

Science.gov (United States)

Amann, T.; Hartmann, J.

2015-12-01

The application of rock flour on suitable land ("Enhanced Weathering") is one proposed strategy to reduce the increase of atmospheric CO2 concentrations. At the same time it is an old and established method to add fertiliser and influence soil properties. Investigations of this method focused on the impact on the carbonate system, as well as on engineering aspects of a large-scale application, but potential side effects were never discussed quantitatively. We analysed about 120,000 geochemically characterised volcanic rock samples from the literature. Applying basic statistics, theoretical release rates of nutrients and potential contaminants by Enhanced Weathering were evaluated for typical rock types. Applied rock material can contain significant amounts of essential or beneficial nutrients (potassium, phosphorus, micronutrients). Their release can partly cover the demand of major crops like wheat, rice or corn, thereby increasing crop yield on degraded soils. However, the concentrations of considered elements are variable within a specific rock type, depending on the geological setting. High heavy metal concentrations are found in (ultra-) basic rocks, the class with the highest CO2 drawdown potential. More acidic rocks contain less or no critical amounts, but sequester less CO2. Findings show that the rock selection determines the capability to supply significant amounts of nutrients, which could partly substitute industrial mineral fertiliser usage. At the same time, the release of harmful trace element has to be considered. Through careful selection of regionally available rocks, benefits could be maximised and drawbacks reduced. The deployment of Enhanced Weathering to sequester CO2 and to ameliorate soils necessitates an ecosystem management, considering the release and fate of weathered elements in plants, soils and water. Cropland with degraded soils would benefit while having a net negative CO2 effect, while other carbon dioxide removal strategies, like

Recovering byproduct heavy minerals from sand and gravel, placer gold, and industrial mineral operations

Energy Technology Data Exchange (ETDEWEB)

Gomes, J.M.; Martinez, G.M.; Wong, M.M.

1979-01-01

The Bureau of Mines, as part of an effort to maximize minerals and metals recovery from domestic resources, has investigated the feasibility of recovering heavy minerals as byproducts from sand and gravel, placer gold, and industrial mineral operations in northern California. Sand samples from about 50 locations were treated by gravity separation to yield heavy-mineral cocentrates (black sands). Mineral compositions of the concentrates were determined by chemical analysis and mineralogical examination. Individual zircon, ilmenite, magnetite, platinum-group metals, thoria, and silica products were prepared from heavy-mineral concentrates by selective separation using low- and high-intensity magnetic, high-tension, and flotation equipment.

Modelling of water-gas-rock geo-chemical interactions. Application to mineral diagenesis in geological reservoirs

International Nuclear Information System (INIS)

Bildstein, Olivier

1998-01-01

Mineral diagenesis in tanks results from interactions between minerals, water, and possibly gases, over geological periods of time. The associated phenomena may have a crucial importance for reservoir characterization because of their impact on petrophysical properties. The objective of this research thesis is thus to develop a model which integrates geochemical functions necessary to simulate diagenetic reactions, and which is numerically efficient enough to perform the coupling with a transport model. After a recall of thermodynamic and kinetic backgrounds, the author discusses how the nature of available analytic and experimental data influenced choices made for the formalization of physical-chemical phenomena and for behaviour laws to be considered. Numerical and computational aspects are presented in the second part. The model is validated by using simple examples. The different possible steps during the kinetic competition between two mineral are highlighted, as well the competition between mineral reaction kinetics and water flow rate across the rock. Redox reactions are also considered. In the third part, the author reports the application of new model functions, and highlights the contribution of the modelling to the understanding of some complex geochemical phenomena and to the prediction of reservoir quality. The model is applied to several diagenetic transformations: cementation of dolomitic limestone by anhydride, illite precipitation, and thermal reduction of sulphates [fr

Mineral-microorganism interactions in Acid Mine Drainage environments: preliminary results

Science.gov (United States)

Carbone, Cristina; Zotti, Mirca; Pozzolini, Marina; Giovine, Marco; Di Piazza, Simone; Mariotti, Mauro; Lucchetti, Gabriella

2014-05-01

Minerals play a key role in controlling the mobility and distribution of metals and metalloids of environmental concern in supergenic environments. These are involved in a variety of processes, spanning the alteration of primary minerals to the formation of secondary authigenic phases and can represent a source or a trap for Potentially Ecotoxic Elements (PTEs). Soil, sediments, and waters heavily polluted with PTEs through AMD processes are a reservoir of a unusual bacteria and fungi well adapted to these toxic environments. Classical studies of biotic weathering have mainly focused on water-mineral interaction and on the ability of microorganism to influence the soil solution chemical composition. In this work, we analyzed two different representative ochreous and greenish-blue AMD colloidal precipitates in order to i) characterize the biota population present in these colloidal minerals and ii) verify the bioaccumulation of PTEs into the fungi and the potential impact of bacteria in the geochemistry of the system. The samples are composed by nanocrystalline goethite which contains high amounts of Fe, Cu, Zn, Pb, and Ni and woodwardite that is characterized by Cu, Zn, Ni, Y, and Ce. These precipitates were examined in order to evaluate the presence of fungal strains and to extract bacteria DNA. The preliminary results of fungi characterization show an interesting and selected mycobiota able to survive under unfavourable environmental conditions. A significant number of fungal strains was isolated in pure culture. Most of them belong to the genus Mucor and Penicillium. It is worth noting the presence of Trametes versicolor, a macrofungal lignicolous species already known for heavy metal biosorption capability from aqueous solution (Gülay et al 2003). The same colloidal precipitates have been processed to extract bacteria DNA, using a specific procedure developed for DNA extraction from sediments. The results gave a good yield of nucleic acids and the positive PCR

CO2 driven weathering vs plume driven weathering as inferred from the groundwater of a persistently degassing basaltic volcano: Mt. Etna

Science.gov (United States)

Liotta, Marcello; D'Alessandro, Walter

2016-04-01

At Mt. Etna the presence of a persistent volcanic plume provides large amounts of volcanogenic elements to the bulk deposition along its flanks. The volcanic plume consists of solid particles, acidic droplets and gaseous species. After H2O and CO2, S, Cl and F represent the most abundant volatile elements emitted as gaseous species from the craters. During rain events acidic gases interact rapidly with droplets lowering the pH of rain. This process favors the dissolution and dissociation of the most acidic gases. Under these conditions, the chemical weathering of volcanic rocks and ashes is promoted by the acid rain during its infiltration. Subsequently during groundwater circulation, chemical weathering of volcanic rocks is also driven by the huge amount of deep magmatic carbon dioxide (CO2) coming up through the volcanic edifice and dissolving in the water. These two different weathering steps occur under very different conditions. The former occurs in a highly acidic environment (pH rates depend strongly on the pH, while the latter usually occurs under slightly acidic conditions since the pH has been already neutralized by the interaction with volcanics rocks. The high content of chlorine is mainly derived from interactions between the plume and rainwater, while the total alkalinity can be completely ascribed to the dissociation of carbonic acid (H2CO3) after the hydration of CO2. The relative contributions of plume-derived elements/weathering and CO2-driven weathering has been computed for each element. In addition, the comparison between the chemical compositions of the bulk deposition and of groundwater provides a new understanding about the mobility of volatile elements. Other processes such as ion exchange, iddingsite formation, and carbonate precipitation can also play roles, but only to minor extents. The proposed approach has revealed that the persistent plume strongly affects the chemical composition of groundwater at Mt. Etna and probably also at other

Characterization of a copper mineral from Rio Grande do Sul (RS, Brazil) by Moessbauer spectroscopy and chemical analysis

Energy Technology Data Exchange (ETDEWEB)

Ribeiro, T H [Rio Grande do Sul Univ., Porto Alegre (Brazil). Inst. de Quimica; Frank, E [Rio Grande do Sul Univ., Porto Alegre (Brazil). Inst. de Fisica; Bristoti, A [Rio Grande do Sul Univ., Porto Alegre (Brazil). Programa de Pos-graduacao de Engenharia Metalurgica e dos Materiais

1980-01-01

A sample from a copper-based mineral is analysed by Moessbauer spectroscopy. The results are compared with those from X-ray diffraction and microscopic analyses. A graphic correlation between the areas in the chalcopyrite spectra and the copper contents determined by chemical analysis is also made.

Niger Republic mineral planning : Part four Second volume : Main mineral substances specific study and their geological context

International Nuclear Information System (INIS)

Franconi, Antoine; Joo', Julien; Zibo, Idde

1981-01-01

This volume describes Niger Republic mineral substances capable of rising economic interest. After relating minerals occurrence , indices and deposits types, conclusions and recommendations have been made for mineral prospecting. Mineral substances described are : Copper, lead and zinc, molybdena, iron, manganese, titanium, vanadium, nickel and chrome ( cobalt and platinoid ), lithium, lignite, diamond and diverse substances rare earth, beryllium, silver, bismuth arsenic and antimony, barytine, alunite, talc and asbestos ( graphite and diatomite) [fr

Clay mineral facies and lateritization in basalts of the southeastern Parana Basin, Brazil

International Nuclear Information System (INIS)

Oliveira, M.T.G. de; Formoso, M.L.L.; Trescases, J.J.; Meunier, A.

1998-01-01

Seventeen samples from two lateritic profiles, each with five facies, were studied. These profiles occur on the old planation surface of the plateau basalts of the southern part of ParanáBasin, Brazil. Optical microscopy, X-ray diffraction, electron microprobe, Mössbauer spectroscopy and Fourier Transform Infrared Spectra were used to obtain information about the nature and chemical composition of each weathering facies. In addition, scanning electron microscopy and analyses of clay minerals were performed to detect microcrystalline environmental changes. Both profiles have two major parts: a loose red-clay latosol separated from an underlying mottled clay and an alterite facies; a stone line may or may not be present between the latosol and the underlying units. In both profiles the latosol consists principally of kaolinite, hematite and goethite. Two alterite facies, shaped by differential weathering, are also present in the lower profile: a halloysite–nontronite clayey matrix with a well developed fissure system occurs in the argillaceous alterite and a network of Al–goethite aggregates is typical of the highly porous cortex of the boulder alterite that is found in the stone line and below it. Gibbsite has crystallized in the large pores of porphyritic boulder alterite but is absent in the small pores of the subaphyric boulder alterite. Clay minerals observed in fissures include halloysite associated with goethite and manganese oxides. The basalt has hydrothermal green-clays (mixed layers and trioctahedral smectites) that formed between primary plagioclase, pyroxene and Ti–magnetite crystals while fresh corestones of the boulder alterite have cryptocrystalline iron-rich material. The study of these profiles shows one principal evolutionary trend for clay minerals. This trend is from smectite and mixed layers that form green clays in altered bedrock at the base of the profile to an intermediate association of nontronite and halloysite in the argillaceous

Transmission Electron Microscopy of Minerals and Rocks

Science.gov (United States)

McLaren, Alex C.

1991-04-01

Of the many techniques that have been applied to the study of crystal defects, none has contributed more to our understanding of their nature and influence on the physical and chemical properties of crystalline materials than transmission electron microscopy (TEM). TEM is now used extensively by an increasing number of earth scientists for direct observation of defect microstructures in minerals and rocks. Transmission Electron Microscopy of Rocks and Minerals is an introduction to the principles of the technique and is the only book to date on the subject written specifically for geologists and mineralogists. The first part of the book deals with the essential physics of the transmission electron microscope and presents the basic theoretical background required for the interpretation of images and electron diffraction patterns. The final chapters are concerned with specific applications of TEM in mineralogy and deal with such topics as planar defects, intergrowths, radiation-induced defects, dislocations and deformation-induced microstructures. The examples cover a wide range of rock-forming minerals from crustal rocks to those in the lower mantle, and also take into account the role of defects in important mineralogical and geological processes.

Different weathering stages indicated by the magnetization of limestones: An example from the southeast Pyrenees, Spain

Science.gov (United States)

Keller, P.; Gehring, A. U.

1992-06-01

Paleomagnetic and structural data from the Pedraforca thrust sheet in the southeast Pyrenees show that the chemical weathering of the late Cretaceous limestones is a multistage process. The first weathering stage, of latest Eocene to early Oligocene age, is indicated by a chemical remanent magnetization carried by hematite. The formation of hematite as the dominant weathering product suggests a subtropical climate in northeast Spain during this period. The second weathering stage is indicated by the presence of goethite, which carries a chemical remanent magnetization parallel to the present earth field. This suggests formation of the goethite since the late Pleistocene under cooler climatic conditions similar to the present-day climate in the Pyrenees.

Chemical composition, mineral content and amino acid and lipid profiles in bones from various fish species.

Science.gov (United States)

Toppe, Jogeir; Albrektsen, Sissel; Hope, Britt; Aksnes, Anders

2007-03-01

The chemical composition, content of minerals and the profiles of amino acids and fatty acids were analyzed in fish bones from eight different species of fish. Fish bones varied significantly in chemical composition. The main difference was lipid content ranging from 23 g/kg in cod (Gadus morhua) to 509 g/kg in mackerel (Scomber scombrus). In general fatty fish species showed higher lipid levels in the bones compared to lean fish species. Similarly, lower levels of protein and ash were observed in bones from fatty fish species. Protein levels differed from 363 g/kg lipid free dry matter (dm) to 568 g/kg lipid free dm with a concomitant inverse difference in ash content. Ash to protein ratio differed from 0.78 to 1.71 with the lowest level in fish that naturally have highest swimming and physical activity. Saithe (Pollachius virens) and salmon (Salmo salar) were found to be significantly different in the levels of lipid, protein and ash, and ash/protein ratio in the bones. Only small differences were observed in the level of amino acids although species specific differences were observed. The levels of Ca and P in lipid free fish bones were about the same in all species analyzed. Fatty acid profile differed in relation to total lipid levels in the fish bones, but some minor differences between fish species were observed.

Antimony sinks in the weathering crust of bullets from Swiss shooting ranges

International Nuclear Information System (INIS)

Ackermann, Sonia; Giere, Reto; Newville, Matthew; Majzlan, Juraj

2009-01-01

Shooting ranges represent sites heavily polluted by Pb, Sb, Cu, Ni, and Zn, which are released during the weathering of bullets. The pristine bullets are made of a Pb-Sb core, Fe mantle, and minor amounts of Cu, Ni, and Zn in an interlayer between the core and mantle. At two selected sampling sites (Losone and Lucerne, both in Switzerland), corroding bullets were collected to determine the sinks of Sb within the weathering crust of the bullets. Bulk Sb concentrations in the crust were found to be as high as 1.3 wt.%. The oxalate-extractable fraction of Fe showed that the amorphous Fe oxides (e.g., ferrihydrite) prevail over goethite and lepidocrocite, which were identified by bulk X-ray diffraction experiments. Crystalline Pb phases are litharge (only found by X-ray diffraction) and cerussite, which result from weathering of the Pb core. No distinct Sb minerals were identified by X-ray diffraction. Investigations with electron microprobe (EMP) showed that Sb is mostly accumulated in those regions in the weathering crust where there is also a high concentration of Fe. In the weathering crust from Losone, such Fe-rich regions with Sb are represented by material that cements or rims silicate mineral grains. The cement was identified as lepidocrocite by micro-Raman analysis. At Lucerne, Sb is found in Fe-oxide aggregates, in sawdust particles where it may be bound to organic matter, or in aggregates enriched in Pb and depleted in Fe. Bulk EXAFS experiments suggested that the Fe oxides are the most important sink for Sb. Our modelling of Sb next-nearest neighbours suggests two types of inner-sphere complexes on the surfaces of Fe oxides. These are edge- and corner-sharing adsorption complexes. Hence, the predominant sink of Sb in the weathering crust of the bullets at the selected shooting ranges is Fe oxides, amorphous or crystalline

A Milestone in Commercial Space Weather: USTAR Center for Space Weather

Science.gov (United States)

Tobiska, W.; Schunk, R. W.; Sojka, J. J.; Thompson, D. C.; Scherliess, L.; Zhu, L.; Gardner, L. C.

2009-12-01

As of 2009, Utah State University (USU) hosts a new organization to develop commercial space weather applications using funding that has been provided by the State of Utah’s Utah Science Technology and Research (USTAR) initiative. The USTAR Center for Space Weather (UCSW) is located on the USU campus in Logan, Utah and is developing innovative applications for mitigating adverse space weather effects in technological systems. Space weather’s effects upon the near-Earth environment are due to dynamic changes in the Sun’s photons, particles, and fields. Of the space environment domains that are affected by space weather, the ionosphere is the key region that affects communication and navigation systems. The UCSW has developed products for users of systems that are affected by space weather-driven ionospheric changes. For example, on September 1, 2009 USCW released, in conjunction with Space Environment Technologies, the world’s first real-time space weather via an iPhone app. Space WX displays the real-time, current global ionosphere total electron content along with its space weather drivers; it is available through the Apple iTunes store and is used around the planet. The Global Assimilation of Ionospheric Measurements (GAIM) system is now being run operationally in real-time at UCSW with the continuous ingestion of hundreds of global data streams to dramatically improve the ionosphere’s characterization. We discuss not only funding and technical advances that have led to current products but also describe the direction for UCSW that includes partnering opportunities for moving commercial space weather into fully automated specification and forecasting over the next half decade.

Illuminating pathways of forest nutrient provision: relative release from soil mineral and organic pools

Science.gov (United States)

Hauser, E.; Billings, S. A.

2017-12-01

Depletion of geogenic nutrients during soil weathering can prompt vegetation to rely on other sources, such as organic matter (OM) decay, to meet growth requirements. Weathered soils also tend to permit deep rooting, a phenomenon sometimes attributed to vegetation foraging for geogenic nutrients. This study examines the extent to which OM recycling provides nutrients to vegetation growing in soils with diverse weathering states. We thus address the fundamental problem of how forest vegetation obtains sufficient nutrition to support productivity despite wide variation in soils' nutrient contents. We hypothesized that vegetation growing on highly weathered soils relies on nutrients released from OM decay to a greater extent than vegetation growing on less weathered, more nutrient-rich substrates. For four mineralogically diverse Critical Zone Observatories (CZO) and Critical Zone Exploratory Network sites, we calculated weathering indices and approximated vegetation nutrient demand and nutrient release from OM decay. We also measured nutrient release rates from OM decay at each site. We then assessed the relationship between degree of soil weathering and the estimated fraction of nutrient demand satisfied by OM derived nutrients. Results are consistent with our hypothesis. The chemical index of alteration (CIA), a weathering index that increases in value with mineral depletion, varies predictably from 90 at the highly weathered Calhoun CZO to 60 at the Catalina CZO, where soils are more recently developed. Estimates of rates of K release from OM decay increase with CIA values. The highest release rate is 2.4 gK m-2 y-1 at Calhoun, accounting for 30% of annual vegetation K uptake; at Catalina, less than 0.5 gm-2 y-1 K is released, meeting 14% of vegetation demand. CIA also co-varies with rooting depth across sites: the deepest roots at the Calhoun sites are growing in soils with the highest CIA values, while the deepest roots at Catalina sites are growing in soils

Caustic Waste-Soil Weathering Reactions and Their Impacts on Trace Contaminant Migration and Sequestration

International Nuclear Information System (INIS)

Dr. Jon Chorover; Dr. Karl T. Mueller; Dr. Peggy O'Day; R. Jeff Serne

2006-01-01

The principal goal of this project was to assess the molecular nature and stability of radionuclide immobilization during weathering reactions in bulk Hanford sediments and their high surface area clay mineral constituents

Structural analysis of heat-treated birch (Betule papyrifera) surface during artificial weathering

International Nuclear Information System (INIS)

Huang Xianai; Kocaefe, Duygu; Kocaefe, Yasar; Boluk, Yaman; Krause, Cornélia

2013-01-01

Highlights: ► Investigate detailed structural changes of heat-treated wood due to weathering. ► Identify connection between physical structural changes and chemical degradation. ► Study effect of heat treatment conditions on weathering degradation process. - Abstract: Effect of artificial weathering on the surface structural changes of birch (Betule papyrifera) wood, heat-treated to different temperatures, was studied using the fluorescence microscopy and the scanning electron microscopy (SEM). Changes in the chemical structure of wood components were analyzed by FTIR in order to understand the mechanism of degradation taking place due to heat treatment and artificial weathering. The results are compared with those of the untreated (kiln-dried) birch. The SEM analysis results show that the effect of weathering on the cell wall of the untreated birch surface is more than that of heat-treated samples. The FTIR spectroscopy results indicate that lignin is the most sensitive component of heat-treated birch to the weathering degradation process. Elimination of the amorphous and highly crystallised cellulose is observed for both heat-treated and untreated wood during weathering. It is also observed that heat treatment increases the lignin and crystallised cellulose contents, which to some extent protects heat-treated birch against degradation due to weathering.

The archaeometry study of the chemical and mineral composition of pottery from Brazil's Northeast

International Nuclear Information System (INIS)

Santos, J.O.; Santos, J.O.; Munita, C.S.; Toyota, R.G.; Oliveira, P.M.S.; Vergne, C.; Silva, R.S.

2009-01-01

Chemical and mineralogical analysis was performed on ceramics and clay samples from Barracao archaeological site located in Baixo Sao Francisco River by means of instrumental neutron activation analysis (INAA) and by differential scanning calorimetry (DSC). The data set was studied by means of cluster analysis (CA) and discriminant analysis (DA). The results showed that the raw material used in ceramics is not local. By using DSC it was possible to discover that the principal minerals in the samples are quartz, feldspars, mica and kaolinite. (author)

An overview of hydrodynamic studies of mineralization

Directory of Open Access Journals (Sweden)

Guoxiang Chi

2011-07-01

Full Text Available Fluid flow is an integral part of hydrothermal mineralization, and its analysis and characterization constitute an important part of a mineralization model. The hydrodynamic study of mineralization deals with analyzing the driving forces, fluid pressure regimes, fluid flow rate and direction, and their relationships with localization of mineralization. This paper reviews the principles and methods of hydrodynamic studies of mineralization, and discusses their significance and limitations for ore deposit studies and mineral exploration. The driving forces of fluid flow may be related to fluid overpressure, topographic relief, tectonic deformation, and fluid density change due to heating or salinity variation, depending on specific geologic environments and mineralization processes. The study methods may be classified into three types, megascopic (field observations, microscopic analyses, and numerical modeling. Megascopic features indicative of significantly overpressured (especially lithostatic or supralithostatic fluid systems include horizontal veins, sand injection dikes, and hydraulic breccias. Microscopic studies, especially microthermometry of fluid inclusions and combined stress analysis and microthermometry of fluid inclusion planes (FIPs can provide important information about fluid temperature, pressure, and fluid-structural relationships, thus constraining fluid flow models. Numerical modeling can be carried out to solve partial differential equations governing fluid flow, heat transfer, rock deformation and chemical reactions, in order to simulate the distribution of fluid pressure, temperature, fluid flow rate and direction, and mineral precipitation or dissolution in 2D or 3D space and through time. The results of hydrodynamic studies of mineralization can enhance our understanding of the formation processes of hydrothermal deposits, and can be used directly or indirectly in mineral exploration.

Oxidation–hydration weathering of uraninite: the current state-of-knowledge

Czech Academy of Sciences Publication Activity Database

Plášil, Jakub

2014-01-01

Roč. 59, č. 2 (2014), s. 99-114 ISSN 1802-6222 R&D Projects: GA ČR GP13-31276P Institutional support: RVO:68378271 Keywords : weathering of uraninite * paragenetic sequence * bond-valence theory * uranyl–oxide minerals * radiogenic lead * thermodynamics Subject RIV: DB - Geology ; Mineralogy Impact factor: 1.405, year: 2014

Age of mineralization of the Nansatsu type gold deposits, Kagoshima, Japan

International Nuclear Information System (INIS)

Izawa, Eiji; Urashima, Yukitoshi; Okubo, Yoshikazu.

1984-01-01

Gold-bearing massive silicified rocks occur in the volcanic piles of the Neogene Tertiary age in the Makurazaki district, southern Kyushu and are termed as the Nansatsu type gold deposits. Currently three mines, Kasuga, Iwato and Akeshi, are operating. The argillized zones consisting mainly of quartz, kaolinite and minor goethite surround the silicified rocks. Alunite series minerals occur in and around the silicified rocks. Ages of mineralization have been discussed for many years but were unanswered. K-Ar dating of selected alunite and alunite-bearing rocks from three mines yields ages of 5.5 - 3.7 m.y. K-Ar ages at Mt. Sonomi of the Kasuga mine (5.5 +- 0.4 m.y.) and at the Arabira orebody of the Iwato mine (4.7 +- 1.0 m.y.) probably represent the ages of gold mineralization. Slightly younger ages at Mt. Iwato of the Iwato mine (4.4 +- 0.7 m.y.) and at the No. 1 orebody of the Akeshi mine (3.7 +- 1.1 m.y.) might reflect possible changes in chemical composition of alunite during weathering after mineralization. Gold-silver mineralization in southern Kyushu took place in the Pliocene to early Pleistocene, except minor silver-rich vein type deposits in the middle Miocene time. This study shows that four values are concordant with each other and indicate the latest Miocene to early Pliocene ages for mineralization of the Nansatsu type gold deposits in the Makurazaki district. The ages are comparable with the vein type gold deposits of the early Pliocene time such as Kushikino (4.0 +- 0.3 m.y.) and Hanakago (4.8 +- 2.9 m.y.). Another gold mineralization were known in the early Pleistocene time such as Hishikari (1.5 +- 0.3 m.y.) and Ora (1.8 +- 0.2 m.y.). At present there seems to be only minor gold mineralization between 4 and 2 m.y. (author)

Vegetation controls on weathering intensity during the last deglacial transition in southeast Africa

Science.gov (United States)

Ivory, Sarah J.; McGlue, Michael M.; Ellis, Geoffrey S.; Lézine, Anne-Marie; Cohen, Andrew S.; Vincens, Annie

2015-01-01

Tropical climate is rapidly changing, but the effects of these changes on the geosphere are unknown, despite a likelihood of climatically-induced changes on weathering and erosion. The lack of long, continuous paleo-records prevents an examination of terrestrial responses to climate change with sufficient detail to answer questions about how systems behaved in the past and may alter in the future. We use high-resolution records of pollen, clay mineralogy, and particle size from a drill core from Lake Malawi, southeast Africa, to examine atmosphere-biosphere-geosphere interactions during the last deglaciation (~18–9 ka), a period of dramatic temperature and hydrologic changes. The results demonstrate that climatic controls on Lake Malawi vegetation are critically important to weathering processes and erosion patterns during the deglaciation. At 18 ka, afromontane forests dominated but were progressively replaced by tropical seasonal forest, as summer rainfall increased. Despite indication of decreased rainfall, drought-intolerant forest persisted through the Younger Dryas (YD) resulting from a shorter dry season. Following the YD, an intensified summer monsoon and increased rainfall seasonality were coeval with forest decline and expansion of drought-tolerant miombo woodland. Clay minerals closely track the vegetation record, with high ratios of kaolinite to smectite (K/S) indicating heavy leaching when forest predominates, despite variable rainfall. In the early Holocene, when rainfall and temperature increased (effective moisture remained low), open woodlands expansion resulted in decreased K/S, suggesting a reduction in chemical weathering intensity. Terrigenous sediment mass accumulation rates also increased, suggesting critical linkages among open vegetation and erosion during intervals of enhanced summer rainfall. This study shows a strong, direct influence of vegetation composition on weathering intensity in the tropics. As climate change will likely impact

Catchment chemostasis revisited: water quality responds differently to variations in weather and climate

Science.gov (United States)

Godsey, Sarah; Kirchner, James

2017-04-01

Solute concentrations in streamflow typically vary systematically with stream discharge, and the resulting concentration-discharge relationships are important signatures of catchment (bio)geochemical processes. Solutes derived from mineral weathering often exhibit decreasing concentrations with increasing flows, suggesting dilution of a kinetically limited weathering flux by a variable flux of water. However, Godsey et al. (2009) showed that concentration-discharge relationships of weathering-derived solutes in 59 headwater catchments were much flatter than this simple dilution model would predict. Instead, their analysis showed that these catchments behaved almost like chemostats, with rates of solute production and/or mobilization that were nearly proportional to water fluxes, on both event and inter-annual time scales. Here we re-examine these findings using data from roughly 1000 catchments, ranging from ˜10 to >1,000,000 km2 in drainage area, and spanning a wide range of lithologic and climatic settings. Concentration-discharge relationships among this much larger set of much larger catchments are broadly consistent with the chemostatic behavior described by Godsey et al. (2009). Among these same catchments, however, site-to-site variations in mean concentrations are strongly (negatively) correlated with long-term average precipitation and discharge, suggesting strong dilution of stream concentrations under long-term leaching of the critical zone. The picture that emerges is one in which, on event and inter-annual time scales, stream solute concentrations are chemostatically buffered by groundwater storage and fast chemical reactions (such as ion exchange), but on much longer time scales, the catchment's chemostatic "set point" is determined by climatically driven critical zone evolution. Examples illustrating the different influences of (short-term) weather and (long-term) climate on water quality will be presented, and their implications will be discussed

Characterization of a Copper mineral from Rio Grande do Sul (RS, Brazil) by Moessbauer spectroscopy and chemical analysis

International Nuclear Information System (INIS)

Ribeiro, T.H.; Frank, E.; Bristoti, A.

1980-01-01

A sample from a copper-based mineral is analysed by Moessbauer spectroscopy. The results are compared with those form X-ray diffraction and microscopic analyses. A graphic correlation between the areas in the chalcopyrite spectra and the copper contents determined by chemical analysis is also made. (C.L.B.) [pt

Surface analytical techniques applied to minerals processing

International Nuclear Information System (INIS)

Smart, R.St.C.

1991-01-01

An understanding of the chemical and physical forms of the chemically altered layers on the surfaces of base metal sulphides, particularly in the form of hydroxides, oxyhydroxides and oxides, and the changes that occur in them during minerals processing lies at the core of a complete description of flotation chemistry. This paper reviews the application of a variety of surface-sensitive techniques and methodologies applied to the study of surface layers on single minerals, mixed minerals, synthetic ores and real ores. Evidence from combined XPS/SAM/SEM studies have provided images and analyses of three forms of oxide, oxyhydroxide and hydroxide products on the surfaces of single sulphide minerals, mineral mixtures and complex sulphide ores. 4 refs., 2 tabs., 4 figs

The effect of chemical admixtures and mineral additives on the properties of self-compacting mortars

Energy Technology Data Exchange (ETDEWEB)

Mustafa Sahmaran; Heru Ari Christianto; Ismail Ozgur Yaman [Middle East Technical University, Ankara (Turkey). Department of Civil Engineering

2006-05-15

Mortar serves as the basis for the workability properties of self-compacting concrete (SCC) and these properties could be assessed by self-compacting mortars (SCM). In fact, assessing the properties of SCM is an integral part of SCC design. The objective of this study was to evaluate the effectiveness of various mineral additives and chemical admixtures in producing SCMs. For this purpose, four mineral additives (fly ash, brick powder, limestone powder, and kaolinite), three superplasticizers (SP), and two viscosity modifying admixtures (VMA) were used. Within the scope of the experimental program, 43 mixtures of SCM were prepared keeping the amount of mixing water and total powder content (Portland cement and mineral additives) constant. Workability of the fresh mortar was determined using mini V-funnel and mini slump flow tests. The setting time of the mortars, were also determined. The hardened properties that were determined included ultrasonic pulse velocity and strength determined at 28 and 56 days. It was concluded that among the mineral additives used, fly ash and limestone powder significantly increased the workability of SCMs. On the other hand, especially fly ash significantly increased the setting time of the mortars, which can, however, be eliminated through the use of ternary mixtures, such as mixing fly ash with limestone powder. The two polycarboxyl based SPs yield approximately the same workability and the melamine formaldehyde based SP was not as effective as the other two.

The radiogenic and stable Sr isotope geochemistry of basalt weathering in Iceland: Role of hydrothermal calcite and implications for long-term climate regulation

Science.gov (United States)

Andrews, M. Grace; Jacobson, Andrew D.

2017-10-01

Several studies have examined the geochemistry of Icelandic rivers to quantify the relationship between basalt weathering and long-term climate regulation. Recent research has suggested that the chemical weathering of hydrothermal and metamorphic calcite contributes significant quantities of HCO3- to the Icelandic riverine flux (Jacobson et al., 2015). Because the HCO3- derives from volcanic CO2 that was sequestered in mineral form prior to atmospheric injection, the strength of the basalt weathering feedback occurring in Iceland may be lower than previously realized. To test these hypotheses, we analyzed the radiogenic and stable Sr isotope composition (87Sr/86Sr and δ88/86Sr) of the same suite of water, rock, and mineral samples as examined in Jacobson et al. (2015), and we developed a simple model of the long-term C cycle that considers the transformation of volcanic CO2 to HCO3- during subsurface silicate weathering, which is a precursor to hydrothermal calcite formation. Interpretations based on 87Sr/86Sr and Ca/Sr ratios suggest that conservative, three-component mixing between basalt, calcite, and atmospheric deposition adequately explains river geochemistry. On average, the δ88/86Sr values of glacial and non-glacial rivers (0.414‰ and 0.388‰, respectively) are generally higher than those for basalt (0.276‰); however, calcite δ88/86Sr values (0.347‰) are also higher than those for basalt and span the range of riverine values. Thus, riverine δ88/86Sr values are also consistent three-component mixing between basalt, calcite, and atmospheric deposition. Isotopic fractionation is not required to explain riverine trends. Finally, model equations for the long-term C cycle demonstrate that subsurface silicate weathering reduces the magnitude of the volcanic CO2 degassing flux, which in turn causes the atmosphere to stabilize at lower pCO2 values compared to the case where no subsurface silicate weathering occurs. However, the proportion of the net

Mineralogical characterization of a highly-weathered soil by the Rietveld Method Caracterização mineralógica de um solo altamente intemperizado pelo Método de Rietveld

Directory of Open Access Journals (Sweden)

André Maurício Brinatti

2010-08-01

Full Text Available The mineralogical characterization through mineral quantification of Brazilian soils by X-ray diffraction data using the Rietveld Method is not common. A mineralogical quantification of an Acric Ferralsol from the Ponta Grossa region, state of Paraná, Brazil, was carried out using this Method with X-Ray Diffraction data to verify if this method was suitable for mineral quantification of a highly-weathered soil. The A, AB and B3 horizons were fractioned to separate the different particle sizes: clay, silt, fine sand (by Stokes Law and coarse sand fractions (by sieving, with the procedure free of chemical treatments. X-ray Fluorescence, Inductively Coupled Plasma Atomic Emission Spectrometry, Infrared Spectroscopy and Mössbauer Spectroscopy were used in order to assist the mineral identification and quantification. The Rietveld Method enabled the quantification of the present minerals. In a general way, the quantitative mineralogical characterization by the Rietveld Method revealed that quartz, gibbsite, rutile, hematite, goethite, kaolinite and halloysite were present in the clay and silt fractions of all horizons. The silt fractions of the deeper horizons were different from the more superficial ones due to the presence of large amounts of quartz. The fine and the coarse sand fractions are constituted mainly by quartz. Therefore, a mineralogical quantification of the finer fraction (clay and silt by the Rietveld Method was successful.A caracterização mineralógica por meio da quantificação dos minerais presentes em solos brasileiros por difração de raios X usando o Método de Rietveld é, ainda, pouco comum. Neste trabalho foi realizada a quantificação mineralógica de um Latossolo Vermelho ácrico da região de Ponta Grossa, Paraná, Brasil, utilizando o Método de Rietveld com dados de Difração de Raios X e também verificado se o método foi adequado na quantificação mineral de um solo altamente intemperizado. Os horizontes A

Characterization of weathered petroleum hydrocarbons during a landfarming bioremediation study

Directory of Open Access Journals (Sweden)

Maletić Snežana

2012-01-01

Full Text Available Landfarming bioremediation was performed over 2 years on soil heavily polluted with weathered oil and oil derivatives: 23200 mg kg-1 of mineral oil, 35300 mg kg-1 total hydrocarbons, and 8.65 mg kg-1 of total PAHs. During the experiment, mineral oil, total hydrocarbon and PAH concentrations decreased by approximately 53%, 27% and 72%, respectively. A GC/MS-Scan was used to identify the crude oil components that persist after bioremediation treatment of contaminated soil and the metabolites generated during this process. The data shows that in weathered-hydrocarbons contaminated soil, the number of initially detected compounds after the bioremediation process further decreased over a 2 year period, and at the same time several new compounds were observed at the end of experiment. Higher persistence was also shown for heavier n-alkanes and branched alkanes, which could be detected over a longer period of time. The analysis highlights the importance of n-alkanes, their substituted derivatives and polycyclic aromatic hydrocarbons as the most significant pollutants.

N2-fixing legumes are linked to enhanced mineral dissolution and microbiome modulations in Neotropical rainforests

Science.gov (United States)

Epihov, Dimitar; Batterman, Sarah; Hedin, Lars; Saltonstall, Kristin; Hall, Jefferson; Leake, Jonathan; Beerling, David

2017-04-01

Legumes represent the dominant family of many tropical forests with estimates of 120 billion legume trees in the Amazon basin alone. Many rainforest legume trees form symbioses with N2-fixing bacteria. In the process of atmospheric N2-fixation large amounts of nitrogen-rich litter are generated, supplying half of all nitrogen required to support secondary rainforest succession. However, it is unclear how N2-fixers affect the biogeochemical cycling of other essential nutrients by affecting the rates of mineral dissolution and rock weathering. Here we show that N2-fixing legumes in young Panamanian rainforests promote acidification and enhance silicate rock weathering by a factor of 2 compared to non-fixing trees. We report that N2-fixers also associate with enhanced dissolution of Al- and Fe-bearing secondary minerals native to tropical oxisols. In legume-rich neighbourhoods, non-fixers benefited from raised weathering rates relative to those of legume-free zones thus suggesting a positive community effect driven by N2-fixers. These changes in weathering potential were tracked by parallel functional and structural changes in the soil and rock microbiomes. Our findings support the view that N2-fixing legumes are central components of biogeochemical cycling, associated with enhanced release of Fe- and Al-bound P and primary mineral products (Mg, Mo). Rainforest legume services therefore bear important implications to short-term C cycling related to forest growth and the long-term C cycle related to marine carbonate deposition fuelled by silicate weathering.

Differences in the importance of weather and weather-based decisions among campers in Ontario parks (Canada)

Science.gov (United States)

Hewer, Micah J.; Scott, Daniel J.; Gough, William A.

2017-10-01

Parks and protected areas represent an important resource for tourism in Canada, in which camping is a common recreational activity. The important relationship between weather and climate with recreation and tourism has been widely acknowledged within the academic literature. Howbeit, the need for activity-specific assessments has been identified as an on-going need for future research in the field of tourism climatology. Furthermore, very little is known about the interrelationships between personal characteristics and socio-demographics with weather preferences and behavioural thresholds. This study uses a stated climate preferences approach (survey responses) to explore differences in the importance of weather and related weather-based decisions among summer campers in Ontario parks. Statistically significant differences were found among campers for each of the four dependent variables tested in this study. Physically active campers placed greater importance on weather but were still more tolerant of adverse weather conditions. Older campers placed greater importance on weather. Campers travelling shorter distances placed greater importance on weather and were more likely to leave the park early due to adverse weather. Campers staying for longer periods of time were less likely to leave early due to weather and were willing to endure longer durations of adverse weather conditions. Beginner campers placed greater importance on weather, were more likely to leave early due to weather and recorded lower temporal weather thresholds. The results of this study contribute to the study of tourism climatology by furthering understanding of how personal characteristics such as gender, age, activity selection, trip duration, distance travelled, travel experience and life cycles affect weather preferences and decisions, focusing this time on recreational camping in a park tourism context.

Optimizing Placement of Weather Stations: Exploring Objective Functions of Meaningful Combinations of Multiple Weather Variables

Science.gov (United States)

Snyder, A.; Dietterich, T.; Selker, J. S.

2017-12-01

Many regions of the world lack ground-based weather data due to inadequate or unreliable weather station networks. For example, most countries in Sub-Saharan Africa have unreliable, sparse networks of weather stations. The absence of these data can have consequences on weather forecasting, prediction of severe weather events, agricultural planning, and climate change monitoring. The Trans-African Hydro-Meteorological Observatory (TAHMO.org) project seeks to address these problems by deploying and operating a large network of weather stations throughout Sub-Saharan Africa. To design the TAHMO network, we must determine where to place weather stations within each country. We should consider how we can create accurate spatio-temporal maps of weather data and how to balance the desired accuracy of each weather variable of interest (precipitation, temperature, relative humidity, etc.). We can express this problem as a joint optimization of multiple weather variables, given a fixed number of weather stations. We use reanalysis data as the best representation of the "true" weather patterns that occur in the region of interest. For each possible combination of sites, we interpolate the reanalysis data between selected locations and calculate the mean average error between the reanalysis ("true") data and the interpolated data. In order to formulate our multi-variate optimization problem, we explore different methods of weighting each weather variable in our objective function. These methods include systematic variation of weights to determine which weather variables have the strongest influence on the network design, as well as combinations targeted for specific purposes. For example, we can use computed evapotranspiration as a metric that combines many weather variables in a way that is meaningful for agricultural and hydrological applications. We compare the errors of the weather station networks produced by each optimization problem formulation. We also compare these

Mineralization of 14C-labeled agrochemicals in soil

International Nuclear Information System (INIS)

Xu Bujin; Huang Xiaohua; Hu Xiuqing; Zhang Yongxi

2001-01-01

14 C-labeled compounds were used to study the mineralization of methamidophos, 2,4-D and metsulfuron in soil. Mineralization rate was influenced by the type of soil, concentration of chemical in the soil, the initial soil microbial population and the nature of the chemical. (author)

Improving aerosol interaction with clouds and precipitation in a regional chemical weather modeling system

Science.gov (United States)

Zhou, C.; Zhang, X.; Gong, S.; Wang, Y.; Xue, M.

2016-01-01

A comprehensive aerosol-cloud-precipitation interaction (ACI) scheme has been developed under a China Meteorological Administration (CMA) chemical weather modeling system, GRAPES/CUACE (Global/Regional Assimilation and PrEdiction System, CMA Unified Atmospheric Chemistry Environment). Calculated by a sectional aerosol activation scheme based on the information of size and mass from CUACE and the thermal-dynamic and humid states from the weather model GRAPES at each time step, the cloud condensation nuclei (CCN) are interactively fed online into a two-moment cloud scheme (WRF Double-Moment 6-class scheme - WDM6) and a convective parameterization to drive cloud physics and precipitation formation processes. The modeling system has been applied to study the ACI for January 2013 when several persistent haze-fog events and eight precipitation events occurred.The results show that aerosols that interact with the WDM6 in GRAPES/CUACE obviously increase the total cloud water, liquid water content, and cloud droplet number concentrations, while decreasing the mean diameters of cloud droplets with varying magnitudes of the changes in each case and region. These interactive microphysical properties of clouds improve the calculation of their collection growth rates in some regions and hence the precipitation rate and distributions in the model, showing 24 to 48 % enhancements of threat score for 6 h precipitation in almost all regions. The aerosols that interact with the WDM6 also reduce the regional mean bias of temperature by 3 °C during certain precipitation events, but the monthly means bias is only reduced by about 0.3 °C.

Improving aerosol interaction with clouds and precipitation in a regional chemical weather modeling system

Directory of Open Access Journals (Sweden)

C. Zhou

2016-01-01

Full Text Available A comprehensive aerosol–cloud–precipitation interaction (ACI scheme has been developed under a China Meteorological Administration (CMA chemical weather modeling system, GRAPES/CUACE (Global/Regional Assimilation and PrEdiction System, CMA Unified Atmospheric Chemistry Environment. Calculated by a sectional aerosol activation scheme based on the information of size and mass from CUACE and the thermal-dynamic and humid states from the weather model GRAPES at each time step, the cloud condensation nuclei (CCN are interactively fed online into a two-moment cloud scheme (WRF Double-Moment 6-class scheme – WDM6 and a convective parameterization to drive cloud physics and precipitation formation processes. The modeling system has been applied to study the ACI for January 2013 when several persistent haze-fog events and eight precipitation events occurred.The results show that aerosols that interact with the WDM6 in GRAPES/CUACE obviously increase the total cloud water, liquid water content, and cloud droplet number concentrations, while decreasing the mean diameters of cloud droplets with varying magnitudes of the changes in each case and region. These interactive microphysical properties of clouds improve the calculation of their collection growth rates in some regions and hence the precipitation rate and distributions in the model, showing 24 to 48 % enhancements of threat score for 6 h precipitation in almost all regions. The aerosols that interact with the WDM6 also reduce the regional mean bias of temperature by 3 °C during certain precipitation events, but the monthly means bias is only reduced by about 0.3 °C.

Mineral and chemical composition of rock core and surface gas composition in Horonobe Underground Research Laboratory project. Phase 1

International Nuclear Information System (INIS)

Hiraga, Naoto; Ishii, Eiichi

2008-02-01

The following three kinds of analyses were conducted for the 1st phase of the Horonobe Underground Research Laboratory Project. Mineral composition analysis of core sample. Whole rock chemical composition analysis of core sample. Surface gas composition analysis. This document summarizes the results of these analyses. (author)

Changes in zinc speciation with mine tailings acidification in a semiarid weathering environment.

Science.gov (United States)

Hayes, Sarah M; O'Day, Peggy A; Webb, Sam M; Maier, Raina M; Chorover, Jon

2011-09-01

High concentrations of residual metal contaminants in mine tailings can be transported easily by wind and water, particularly when tailings remain unvegetated for decades following mining cessation, as is the case in semiarid landscapes. Understanding the speciation and mobility of contaminant metal(loid)s, particularly in surficial tailings, is essential to controlling their phytotoxicities and to revegetating impacted sites. In prior work, we showed that surficial tailings samples from the Klondyke State Superfund Site (AZ, USA), ranging in pH from 5.4 to 2.6, represent a weathering series, with acidification resulting from sulfide mineral oxidation, long-term Fe hydrolysis, and a concurrent decrease in total (6000 to 450 mg kg(-1)) and plant-available (590 to 75 mg kg(-1)) Zn due to leaching losses and changes in Zn speciation. Here, we used bulk and microfocused Zn K-edge X-ray absorption spectroscopy (XAS) data and a six-step sequential extraction procedure to determine tailings solid phase Zn speciation. Bulk sample spectra were fit by linear combination using three references: Zn-rich phyllosilicate (Zn(0.8)talc), Zn sorbed to ferrihydrite (Zn(adsFeOx)), and zinc sulfate (ZnSO(4) · 7H(2)O). Analyses indicate that Zn sorbed in tetrahedral coordination to poorly crystalline Fe and Mn (oxyhydr)oxides decreases with acidification in the weathering sequence, whereas octahedral zinc in sulfate minerals and crystalline Fe oxides undergoes a relative accumulation. Microscale analyses identified hetaerolite (ZnMn(2)O(4)), hemimorphite (Zn(4)Si(2)O(7)(OH)(2) · H(2)O) and sphalerite (ZnS) as minor phases. Bulk and microfocused spectroscopy complement the chemical extraction results and highlight the importance of using a multimethod approach to interrogate complex tailings systems.

Sorption kinetics and chemical forms of Cd(II) sorbed by thiol-functionalized 2:1 clay minerals

International Nuclear Information System (INIS)

Malferrari, D.; Brigatti, M.F.; Laurora, A.; Pini, S.; Medici, L.

2007-01-01

The interaction between Cd(II) in aqueous solution and two 2:1 expandable clay minerals (i.e., montmorillonite and vermiculite), showing different layer charge, was addressed via batch sorption experiments on powdered clay minerals both untreated and amino acid (cysteine) treated. Reaction products were characterized via X-ray powder diffraction (XRDP), chemical analysis (elemental analysis and atomic absorption spectrophotometry), thermal analysis combined with evolved gasses mass spectrometry (TGA-MSEGA) and synchrotron-based X-ray absorption spectroscopy via extended X-ray absorption fine structure (EXAFS) characterization. Sorption isotherms for Cd(II) in presence of different substrates, shows that Cd(II) uptake depends both on Cd(II) starting concentration and the nature of the substrate. Thermal decomposition of Cd-cysteine treated clay minerals evidences the evolution of H 2 O, H 2 S, NO 2 , SO 2 , and N 2 O 3 . These results are well consistent with XRDP data collected both at room and at increasing temperature and further stress the influence of the substrate, in particular cysteine, on the interlayer. EXAFS studies suggest that Cd(II) coordinates with oxygen atoms, to give monomer complexes or CdO molecules, either on the mineral surface and/or in the interlayer. For Cd-cysteine complexes EXAFS data agree with the existence of Cd-S clusters, thus suggesting a predominant role of the thiol group in the bonding of Cd with the amino acid