Near-surface clay authigenesis in exhumed fault rock of the Alpine Fault Zone (New Zealand); O-H-Ar isotopic, XRD and chemical analysis of illite and chlorite

NASA Astrophysics Data System (ADS)

Boles, Austin; Mulch, Andreas; van der Pluijm, Ben

2018-06-01

Exhumed fault rock of the central Alpine Fault Zone (South Island, New Zealand) shows extensive clay mineralization, and it has been the focus of recent research that aims to describe the evolution and frictional behavior of the fault. Using Quantitative X-ray powder diffraction, 40Ar/39Ar geochronology, hydrogen isotope (δD) geochemistry, and electron microbeam analysis, we constrain the thermal and fluid conditions of deformation that produced two predominant clay phases ubiquitous to the exposed fault damage zone, illite and chlorite. Illite polytype analysis indicates that most end-member illite and chlorite material formed in equilibrium with meteoric fluid (δD = -55 to -75‰), but two locations preserve a metamorphic origin of chlorite (δD = -36 to -45‰). Chlorite chemical geothermometry constrains crystal growth to T = 210-296 °C. Isotopic analysis also constrains illite growth to T < 100 °C, consistent with the mineralogy, with Ar ages <0.5 Ma. High geothermal gradients in the study area promoted widespread, near-surface mineralization, and limited the window of clay authigenesis in the Alpine Fault Zone to <5 km for chlorite and <2 km for illite. This implies a significant contrast between fault rock exposed at the surface and that at depth, and informs discussions about fault strength, clays and frictional behavior.

PROGRESS REPORT ON GEOLOGIC STUDIES OF THE RANGER OREBODIES, NORTHERN TERRITORY, AUSTRALIA.

USGS Publications Warehouse

Nash, J. Thomas; Frishman, David; ,

1985-01-01

The Ranger No. 1 and No. 3 orebodies contain about 124,000 tonnes U//3O//8 in highly chloritized metasediments of the lower Proterozoic Cahill Formation within about 500 m of the projected sub-Kombolgie Formation unconformity. In both orebodies, oxidized and reduced uranium minerals occur chiefly in quartzose schists that have highly variable amounts of muscovite, sericite, and chlorite. The effects of several periods of alteration are pervasive in the vicinity of orebodies where biotite and garnet are altered to chlorite, and feldspars to white mica or chlorite. Oxidized uranium minerals, associated with earthy iron oxides, occur from the surface to a depth of about 60 m. Below the oxidized zone, uranium occurs chiefly as uraninite and pitchblende disseminated through thick sections of quartz-chlorite-muscovite schist and has no apparent association with graphite or sulphides. The geologic age(s) of uranium emplacement are obscure because there are few age criteria. Reduced uranium minerals are younger than 1. 8-b. y. -old granite dykes, and some occur locally in 1. 65-b. y. -old Kombolgie Formation.

Magnesium isotopic behavior during the formation of chlorite-rich hydrothermal sediment in the middle Okinawa Trough

NASA Astrophysics Data System (ADS)

Shao, H.; Yang, S.; Teng, F. Z.; Cai, D.; Humphris, S. E.

2016-12-01

Chlorite is a common alteration product during water-rock reactions in seafloor hydrothermal systems. This chlorite is commonly characterized by high concentrations of magnesium. However, the source of the Mg and its behavior during hydrothermal alteration have yet to be clarified. Mg isotopes have been used in recent years to investigate a variety of geological processes, including low temperature weathering and metamorphism processes, and Mg cycling in sediments. In this study, we investigate the source of Mg and its behavior in chlorite-rich sediments collected during IODP Expedition 331 from the active hydrothermal Iheya North Knoll field in the middle Okinawa Trough — an intra-continental rift in continental crust. This area is characterized by hemipelagic muds with interbedded thick layers of felsic pumiceous volcanic material. Based on mineralogical, geochemical, and isotopic data, we have previously suggested that the chlorite-rich sediments resulted from hydrothermal alteration of the pumiceous layers at temperatures of 220-300°C. Prior to Mg isotope analysis, all selected samples were pretreated with 1N HCl in order to remove carbonates and other unstable minerals, and measurements were made on both the residues (mainly chlorite) and leachates, as well as on bulk samples. The residues are expected to show higher δ26Mg than the leachates reflecting the Mg isotopic signature of the pumiceous material precursor and provide insight into the behavior of Mg isotopes during the high-temperature hydrothermal processes.

Examination of chloritization of biotite as a tool for reconstructing the physicochemical parameters of mineralization and associated alteration in the Zafarghand porphyry copper system, Ardestan, Central Iran: mineral-chemistry and stable isotope analyses

NASA Astrophysics Data System (ADS)

Aminroayaei Yamini, Maryam; Tutti, Faramarz; Aminoroayaei Yamini, Mohammad Reza; Ahmadian, Jamshid; Wan, Bo

2017-10-01

The chloritization of biotite and stable isotopes of silicate have been studied for the Zafarghand porphyry copper deposit, Ardestan, Iran. The studied area, in the central part of the Urumieh-Dokhtar magmatic belt, contains porphyry-style Cu mineralization and associated hydrothermal alteration within the Miocene (19-26 Ma, Zircon U-Pb age) granodioritc stock and adjacent andesitic to rhyodacitic volcanic rocks (ca. 56 Ma, zircon U-Pb age). The primary and secondary biotite that formed during potassic alteration in this porphyry and these volcanic host rocks are variably chloritized. Chloritization of biotite pseudomorphically is characterized by an increase in MgO, FeOt, and MnO, with decreasing in SiO2, K2O, and TiO2. Based on the Ti-in-biotite geothermometer of Henry et al. (Am Mineral 90:316-328, 2005) and Al-in-chlorite geothermometer of Cathelineau (Clay Miner 23:417-485, 1988), crystallization temperatures of primary biotite representative of magmatic conditions and later chloritization temperature range from 617° to 675 °C ± 24 °C and 177° to 346 °C, respectively. Calculated isotopic compositions of fluids that chloritized primary and secondary biotite display isotopic compositions of 1.1 to 1.7 per mil for δ18O and -19.9 to -20.5 per mil for δD consistent with meteoric water. Sericite, barren, and A-type-quartz veins from phyllic alteration were produced by mixed magmatic and meteoric water with δ18O values from -2.8 to 2.5 and δD values of ˜ -23 per mil; the narrow range of δD values of the propylitic epidote may be due to a meteoric water with δ18O values from 0.8 to 1.6 and δD values from -14.6 to -16.9 per mil.

Scales of equilibrium and disequilibrium during cleavage formation in chlorite and biotite-grade phyllites, SE Vermont

USGS Publications Warehouse

McWilliams, C.K.; Wintsch, R.P.; Kunk, Michael J.

2007-01-01

Detailed electron microprobe analyses of phyllosilicates in crenulated phyllites from south-eastern Vermont show that grain-scale zoning is common, and sympathetic zoning in adjacent minerals is nearly universal. We interpret this to reflect a pressure-solution mechanism for cleavage development, where precipitation from a very small fluid reservoir fractionated that fluid. Multiple analyses along single muscovite, biotite and chlorite grains (30–200 μm in length) show zoning patterns indicating Tschermakitic substitutions in muscovite and both Tschermakitic and di/trioctahedral substitutions in biotite and chlorite. Using cross-cutting relationships and mineral chemistry it is shown that these patterns persist in cleavages produced at metamorphic conditions of chlorite-grade, chlorite-grade overprinted by biotite-grade and biotite-grade. Zoning patterns are comparable in all three settings, requiring a similar cleavage-forming mechanism independent of metamorphic grade. Moreover, the use of 40Ar/39Ar geochronology demonstrates this is true regardless of age. Furthermore, samples with chlorite-grade cleavages overprinted by biotite porphyroblasts suggest the closure temperatures for the diffusion of Al, Si, Mg and Fe ions are greater than the temperature of the biotite isograd (>∼400 °C). Parallel and smoothly fanning tie lines produced by coexisting muscovite–chlorite, and muscovite–biotite pairs on compositional diagrams demonstrate effectively instantaneous chemical equilibrium and probably indicate simultaneous crystallization.These results do not support theories suggesting cleavages form in fluid-dominated systems. If crenulation cleavages formed in systems in which the chemical potentials of all major components are fixed by an external reservoir, then the compositions of individual grains defining these cleavages would be uniform. On the contrary, the fine-scale chemical zoning observed probably reflects a grain-scale process consistent with a pressure-solution mechanism in which the aqueous activities of major components are defined by local dissolution and precipitation. Thus the role of fluids was probably limited to one of catalysing pressure-solution and fluids apparently did not drive cleavage development.

Production of bio-sugar and bioethanol from coffee residue (CR) by acid-chlorite pretreatment.

PubMed

Kim, Ho Myeong; Choi, Yong-Soo; Lee, Dae-Seok; Kim, Yong-Hwan; Bae, Hyeun-Jong

2017-07-01

Nowadays, coffee residue (CR) after roasting is recognized as one of the most useful resources in the world for producing the biofuel and bio-materials. In this study, we evaluated the potential of bio-sugar and bioethanol production from acid-chlorite treated CR. Notably, CR treated three times with acid-chlorite after organic solvent extraction (OSE-3), showed the high monosaccharide content, and the efficient sugar conversion yield compared to the other pretreatment conditions. The OSE-3 (6% substrate loading, w/v) can produce bio-sugar (0.568g/g OSE-3). Also, simultaneous saccharification and fermentation (SSF) produced ethanol (0.266g/g OSE-3), and showed an ethanol conversion yield of 73.8% after a 72-h reaction period. These results suggest that acid-chlorite pretreatment can improve the bio-sugar and bioethanol production of CR by removing the phenolic and brown compounds. Copyright © 2017 Elsevier Ltd. All rights reserved.

Hydrothermal and metamorphic berthierine from the Kidd Creek volcanogenic massive sulfide deposit, Timmins, Ontario

USGS Publications Warehouse

Slack, J.F.; Wei-Teh, Jiang; Peacor, D.R.; Okita, P.M.

1992-01-01

Berthierine, a 7 A?? Fe-Al member of the serpentine group, occurs in the footwall stringer zone of the Archean Kidd Creek massive sulfide deposit, associated with quartz, muscovite, chlorite, pyrite, sphalerite, chalcopyrite, and local tourmaline, cassiterite, and halloysite. Petrographic and scanning electron microscopic (SEM) studies reveal different types of berthierine occurrences, including interlayers within the rims on deformed chlorite, intergrowths with muscovite and halloysite, and discrete coarse grains. This is the first reported occurrence of berthierine from volcanogenic massive sulfide deposits. Textural relations suggest that most of the berthierine formed as a primary hydrothermal mineral at relatively high temperatures (~350??C) in the footwall stringer zone, probably by the replacement of a pre-existing aluminous phase such as muscovite or chlorite. However, the intergrowth textures observed by SEM and TEM suggest that some of the berthierine originated by syn- or post-metamorphic replacement of chlorite. -from Authors

Chlorite (sodium salt)

Integrated Risk Information System (IRIS)

Chlorite ( sodium salt ) ; CASRN 7758 - 19 - 2 Human health assessment information on a chemical substance is included in the IRIS database only after a comprehensive review of toxicity data , as outlined in the IRIS assessment development process . Sections I ( Health Hazard Assessments for Noncarc

Wynoochee Dam Foundation Report

DTIC Science & Technology

1988-01-01

schists and in propylitized andesite volcanic rocks. Tests on chlorite-bearing graywackes (Lumni Island and Robe Quarry, Seattle District) and... propylitized chlorite-bearing andesites (Blue River and Lookout Point Dams, Portland District) have shown these rocks to be durable materials with only minor

Oxygen isotope fractionation between chlorite and water from 170 to 350 C: A preliminary assessment based on partial exchange and fluid/rock experiments

DOE Office of Scientific and Technical Information (OSTI.GOV)

Cole, D.R.; Ripley, E.M.

1999-02-01

Oxygen isotope fractionations in laboratory systems have been determined between chlorite and water at 170--350 C. In one series of experiments, the Northrop-Clayton partial exchange method was used where three (sometimes four) isotopically different waters were reacted with chlorite. The percents of exchange determined for the four times from shortest to longest are 4.4, 6.5, 8.0, and 11.9. The fractionations calculated from the Northrop and Clayton method are in modest agreement for the four run durations: 0.13, 0.26, {minus}0.46, and {minus}0.55 per mil. Errors associated with each of these fractionations are quite large (e.g. {+-}1.2 per mil for the longestmore » run). The value determined for the longest run of {approximately}20 weeks is the most reliable of the group and compares very closely with a value of {approximately}{minus}0.7 per mil estimated by Wenner and Taylor based on natural chlorides. Good agreement is also observed with the estimates, {minus}1.2 and {minus}1.3% calculated at 350 C for chlorite compositions with [({Sigma}Fe)/{Sigma}Fe + Mg] = 0.313 and 0.444, respectively, from equations given by Savin and Lee based on their empirical bond-type method. Additional fractionation data have been estimated from hydrothermal granite-fluid experiments where chlorite formed from biotite. Detailed thin section, scanning electron microscope (SEM), x-ray diffraction (XRD), and electron microprobe analyses demonstrate that biotite is altered exclusively to chlorite in 13 granite-fluid experiments conducted at the following conditions: T = 170--300 C, P = vapor saturation - 200 b, salinity = H{sub 2}O, 0.1 and 1 m NaCl, fluid/biotite mass ratios = 3--44, run durations = 122--772 h. The amount of chlorite, quantified through point counting and XRD, increased with increasing temperature, salinity, and time. The isotope compositions of chlorite were calculated from mass balance and compared to the final measured {delta}{sup 18}O of the fluids. The 10{sup 3}ln {alpha} values averaged 0.14, 0.8 and 2.9 per mil for 300, 250, and 200 C, respectively. A least-squares regression model of the combined data set (all T`s) is presented.« less

Temperature micro-mapping and redox conditions of a chlorite zoning pattern in green-schist facies fault zone

NASA Astrophysics Data System (ADS)

Trincal, Vincent; Lanari, Pierre; Lacroix, Brice; Buatier, Martine D.; Charpentier, Delphine; Labaume, Pierre; Muñoz, Manuel

2014-05-01

Faults are major discontinuities driving fluid flows and playing a major role in precipitation of ore deposits. Mineral paragenesis and crystal chemistry depend on Temperature (T) condition, fluid composition but also on the redox environment of precipitation. The studied samples come from the Pic de Port Vieux thrust sheet, a minor thrust sheet associated to Gavarnie thrust fault zone (Central Pyrenees). The Pic de Port Vieux Thrust sheet comprises a 1-20 meter thick layer of Triassic red beds and mylonitized Cretaceous limestone. The thrust sheet is affected by faults and cleavage; the other important deformation product is a set of veins filled by quartz and chlorite. Microstructural and mineralogical investigations were performed based on the previous work of Grant (1992). The crystallization of chlorite is syn-tectonic and strongly controlled by the fluid circulation during the Gavarnie thrust sheet emplacement. Chlorite precipitated in extension veins, crack-seal shear veins or in open cavities. The chlorite filling the open cavities occurs as pseudo-uniaxial plates arranged in rosette-shaped aggregates. These aggregates appear to have developed as a result of radial growth of the chlorite platelets. According to point and microprobe X-ray images, these chlorites display oscillatory chemical zoning patterns with alternating iron rich and magnesium rich bands. The chlorite composition ranges from Fe rich pole (Si2.62Al1.38O10(Al1.47Fe1.87Mg2.61)6(OH)8) to Mg rich pole (Si2.68Al1.31O10(Al1.45Fe1.41Mg3.06)6(OH)8). In metamorphic rocks, zoning pattern or rimmed minerals results for varying P or T conditions and can be used to unravel the P-T history of the sample. In the present study, temperature maps are derived from standardized microprobe X-ray images using the program XMapTools (Lanari et al 2014). The (Fe3+/Fetot) value in chlorite was directly measured using μXANES spot analyses collected at the Fe-K edge. The results indicate a homogeneous temperature of 300-350° C throughout the crystallization. This result excludes the T as the main parameter to explain the Fe and Mg zoning patterns. Several other origins can be proposed and discussed in order to understand zoning patterns such as fluid chemistry, pressure, pH or redox variations of the fluid. Grant, N.T., 1992. Post-emplacement extension within a thrust sheet from the central Pyrenees. Journal of the Geological Society 149, 775-792. Lanari, P., Vidal, O., De Andrade, V., Dubacq, B., Lewin, E., Grosch, E.G., Schwartz, S., 2014. XMapTools: A MATLAB©-based program for electron microprobe X-ray image processing and geothermobarometry. Computers & Geosciences 62, 227-240.

Sorption and reduction of selenite on chlorite surfaces in the presence of Fe(II) ions.

PubMed

Baik, Min Hoon; Lee, Seung Yeop; Jeong, Jongtae

2013-12-01

The sorption and reduction of selenite on chlorite surfaces in the presence of Fe(II) ions were investigated as a function of pH, Se(IV) concentration, and Fe(II) concentration under an anoxic condition. The sorption of Se(IV) onto chlorite surfaces followed the Langmuir isotherm regardless of the presence of Fe(II) ions in the solution. The Se(IV) sorption was observed to be very low at all pH values when the solution was Fe(II)-free or the concentration of Fe(II) ions was as low as 0.5 mg/L. However, the Se(IV) sorption was enhanced at a pH > 6.5 when the Fe(II) concentration was higher than 5 mg/L because of the increased sorption of Fe(II) onto the chlorite surfaces. XANES (X-ray absorption near edge structure) spectra of the Se K-edge showed that most of the sorbed Se(IV) was reduced to Se(0) by Fe(II) sorbed onto the chlorite surfaces, especially at pH > 9. The combined results of field-emission scanning electron microscopy (FE-SEM) and X-ray diffraction (XRD) also showed that elemental selenium and goethite were formed and precipitated on the chlorite surfaces during the sorption of selenite. Consequently it can be concluded that Se(IV) can be reduced to Se(0) in the presence of Fe(II) ions by the surface catalytic oxidation of Fe(II) into Fe(III) and the formation of goethite at neutral and particularly alkaline conditions. Thus the mobility of selenite in groundwater is expected to be reduced by the presence of a relatively higher concentration of Fe(II) in subsurface environments. Copyright © 2013 Elsevier Ltd. All rights reserved.

Development of an automated on-line electrochemical chlorite ion sensor.

PubMed

Myers, John N; Steinecker, William H; Sandlin, Zechariah D; Cox, James A; Gordon, Gilbert; Pacey, Gilbert E

2012-05-30

A sensor system for the automatic, in-line, determination of chlorite ion is reported. Electroanalytical measurements were performed in electrolyte-free liquids by using an electrochemical probe (EC), which enables in-line detection in high-resistance media such as disinfected water. Cyclic voltammetry scan rate studies suggest that the current arising from the oxidation of chlorite ion at an EC probe is mass-transfer limited. By coupling FIA with an EC probe amperometric cell, automated analysis was achieved. This sensor is intended to fulfill the daily monitoring requirements of the EPA DBP regulations for chlorite ion. Detection limits of 0.02-0.13 mg/L were attained, which is about one order of magnitude below the MRDL. The sensor showed no faradaic signal for perchlorate, chlorate, or nitrate. The lifetime and stability of the sensor were investigated by measuring calibration curves over time under constant-flow conditions. Detection limits of <0.1 mg/L were repeatedly achieved over a period of three weeks. Copyright © 2012 Elsevier B.V. All rights reserved.

“Development of an Automated On-line Electrochemical Chlorite Ion Sensor”

PubMed Central

Myers, John N.; Steinecker, William H.; Sandlin, Zechariah D.; Cox, James A.; Gordon, Gilbert; Pacey, Gilbert E.

2012-01-01

A sensor system for the automatic, in-line, determination of chlorite ion is reported. Electroanalytical measurements were performed in electrolyte-free liquids by using an electrochemical probe (EC), which enables in-line detection in high-resistance media such as disinfected water. Cyclic voltammetry scan rate studies suggest that the current arising from the oxidation of chlorite ion at an EC probe is mass-transfer limited. By coupling FIA with an EC probe amperometric cell, automated analysis was achieved. This sensor is intended to fulfill the daily monitoring requirements of the EPA DBP regulations for chlorite ion. Detection limits of 0.02-0.13 mg/L were attained, which is about one order of magnitude below the MRDL. The sensor showed no faradaic signal for perchlorate, chlorate, or nitrate. The lifetime and stability of the sensor were investigated by measuring calibration curves over time under constant-flow conditions. Detection limits of <0.1 mg/L were repeatedly achieved over a period of three weeks. PMID:22608440

Manganese oxides and associated minerals as constituents of dispersed mineralization of metasomatic rocks in the Dukat ore field

NASA Astrophysics Data System (ADS)

Filimonova, L. G.; Sivtsov, A. V.; Trubkin, N. V.

2010-08-01

Lithiophorite and coronadite—varieties of vernadite and todorokite—make up finely dispersed colloform mixtures along with minor grains and nanoparticles of aluminosilicates and ore minerals in metasomatic rocks of the Dukat ore field, which were formed in local areas of fluid and hydrothermal-solution discharge at the upper level of the ore-forming system. Fe-vernadite associates with feroxyhyte, magnetite, apatite, K-feldspar, native silver, and acanthite in greisenized granitoids and with epidote, cerianite, plattnerite, and Fe-chlorite in quartz-garnet-chlorite propylites. Todorokite with high Pb, Tl, and Sn contents associates with epidote, albite, bitumen, and native silver in quartz-epidote-chlorite propylites. Al-vernadite, coronadite, and lithiophorite associate with opal, kaolinite, Fe-chlorite, zincite, uraninite, native silver, and acanthite in argillisites. These data allowed us to estimate the conditions of manganese accumulation in the epithermal ore-forming system and deposition conditions of Mn-rich, finely dispersed mineral mixtures in mineralized zones hosted in metasomatic rocks of the ore field.

Tetramethylbenzidine method for monitoring the free available chlorine and microbicidal activity of chlorite-based sanitizers under organic-matter-rich environments.

PubMed

Yamaoka, H; Nakayama-Imaohji, H; Horiuchi, I; Yamasaki, H; Nagao, T; Fujita, Y; Maeda, H; Goda, H; Kuwahara, T

2016-01-01

Chlorine is a principal disinfectant for food and environmental sanitation. Monitoring of free available chlorine (FAC) is essential for ensuring the efficacy of food disinfection processes that rely on chlorine. N,N-diethyl-p-phenylenediamine (DPD) is commonly used for FAC monitoring. However, here, we show that upon contact with bovine serum albumin (BSA) or broiler carcasses, chlorite (HClO2 )-based sanitizers acquire a pink colour, which can interfere with measurement of oxidized DPD absorbance at 513-550 nm. Alternatively, the pink colour did not interfere with 3,3',5,5'-tetramethylbenzidine (TMB)-based FAC monitoring. The FAC levels of NaClO and weakly acidified chlorous acid water (WACAW) were first adjusted by the TMB method and the killing activity of these sanitizers towards methicillin-resistant Staphylococcus aureus (MRSA) and feline calicivirus (FCV) was compared in the presence or absence of 0·5% BSA. At 200 ppm FAC, NaClO lost its bactericidal activity against MRSA after 10-min incubation with 0·5% BSA. Meanwhile, under the same conditions WACAW reduced the number of bacteria to below the detection limit. Similar results were obtained with FCV, indicating that the chlorite-based WACAW sanitizer is relatively stable under organic-matter-rich conditions. Moreover, TMB is suitable for in situ FAC monitoring of chlorite-based sanitizers in food and environmental disinfection processes. For practical applications of chlorine in food processing, monitoring of FAC is critical to validate disinfection efficacy. In this study we found that chlorite-based sanitizers acquired a pink colour upon contact with BSA or broiler carcasses. This pink colour interfered with FAC monitoring by methods that measure oxidized N,N-diethyl-p-phenylenediamine absorbance between 513-550 nm. Alternatively, FAC levels of chlorite-based sanitizers could be monitored using the absorbance of 3,3',5,5'-tetramethylbenzidine at 650 nm, which does not overlap with the acquired pink colour. These data provide valuable information for safety management of disinfection processes that use chlorite-based sanitizers. © 2015 The Society for Applied Microbiology.

The importance of the location of sodium chlorite application in a multipollutant flue gas cleaning system.

PubMed

Krzyzynska, Renata; Hutson, Nick D

2012-06-01

In this study, removing sulfur dioxide (SO2), nitrogen oxides (NO(x)), and mercury (Hg) from simulated flue gas was investigated in two laboratory-sized bubbling reactors that simulated an oxidizing reactor (where the NO and Hg(0) oxidation reactions are expected to occur) and a wet limestone scrubber, respectively. A sodium chlorite solution was used as the oxidizing agent. The sodium chlorite solution was an effective additive that enhanced the NO(x), Hg, and SO2 capture from the flue gas. Furthermore, it was discovered that the location of the sodium chlorite application (before, in, or after the wet scrubber) greatly influences which pollutants are removed and the amount removed. This effect is related to the chemical conditions (pH, absence/presence of particular gases) that are present at different positions throughout the flue gas cleaning system profile. The research results indicated that there is a potential to achieve nearly zero SO2, NO(x), and Hg emissions (complete SO2, NO, and Hg removals and -90% of NO(x) absorption from initial values of 1500 ppmv of SO2, 200 ppmv of NO(x), and 206 microg/m3 of Hg(0)) from the flue gas when sodium chlorite was applied before the wet limestone scrubber. However applying the oxidizer after the wet limestone scrubber was the most effective configuration for Hg and NO(x) control for extremely low chlorite concentrations (below 0.002 M) and therefore appears to be the best configuration for Hg control or as an additional step in NO(x) recleaning (after other NO(x) control facilities). The multipollutant scrubber, into which the chlorite was injected simultaneously with the calcium carbonate slurry, appeared to be the least expensive solution (when consider only capital cost), but exhibited the lowest NO(x) absorption at -50%. The bench-scale test results presented can be used to develop performance predictions for a full- or pilot-scale multipollutant flue gas cleaning system equipped with wet flue gas desulfurization scrubber.

Kikuchi-Fujimoto disease presenting after consumption of ‘Miracle Mineral Solution’ (sodium chlorite)

PubMed Central

Loh, John Ming Ren; Shafi, Humaira

2014-01-01

We present a case report of a 41-year-old woman of Malay ethnicity who presented with an 11-day history of fever and left-sided lymphadenopathy after consuming ‘Miracle Mineral Solution’ (sodium chlorite solution) for the first time. A diagnosis of Kikuchi-Fujimoto disease was established via lymph node biopsy after other differentials were excluded. The aetiology of Kikuchi-Fujimoto disease remains controversial, but viral, autoimmune and physicochemical causes have been suggested as possibilities. In this case, we hypothesise that oxidative injury from sodium chlorite initiated an inflammatory response, which triggered the onset of Kikuchi-Fujimoto disease. PMID:25422331

Chlorite dissolution kinetics at pH 3–10 and temperature to 275°C

DOE PAGES

Smith, Megan M.; Carroll, Susan A.

2015-12-02

Sheet silicates and clays are ubiquitous in geothermal environments. Their dissolution is of interest because this process contributes to scaling reactions along fluid pathways and alteration of fracture surfaces which could affect reservoir permeability. Here, in order to better predict the geochemical impacts on long-term performance of engineered geothermal systems, we have measured chlorite dissolution and developed a generalized kinetic rate law applicable over an expanded range of solution pH and temperature. Chlorite, (Mg,Al,Fe) 12(Si,Al) 8O 20(OH) 16, commonly occurs in many geothermal host rocks as either a primary mineral or alteration product.

Chlorite dissolution kinetics at pH 3–10 and temperature to 275°C

DOE Office of Scientific and Technical Information (OSTI.GOV)

Smith, Megan M.; Carroll, Susan A.

Sheet silicates and clays are ubiquitous in geothermal environments. Their dissolution is of interest because this process contributes to scaling reactions along fluid pathways and alteration of fracture surfaces which could affect reservoir permeability. Here, in order to better predict the geochemical impacts on long-term performance of engineered geothermal systems, we have measured chlorite dissolution and developed a generalized kinetic rate law applicable over an expanded range of solution pH and temperature. Chlorite, (Mg,Al,Fe) 12(Si,Al) 8O 20(OH) 16, commonly occurs in many geothermal host rocks as either a primary mineral or alteration product.

Mineralogical, IR-spectral and geochemical monitoring of hydrothermal alteration in a deformed and metamorphosed Jurassic VMS deposit at Arroyo Rojo, Tierra del Fuego, Argentina

NASA Astrophysics Data System (ADS)

Biel, C.; Subías, I.; Acevedo, R. D.; Yusta, I.; Velasco, F.

2012-04-01

The Arroyo Rojo Zn-Pb-Cu volcanogenic massive sulfide deposit is the main deposit of the Fin del Mundo District in the Fuegian Andes, Argentina. This deposit is hosted by a Middle Jurassic volcanic and volcanoclastic sequence forming the Lemaire Formation. The latter consists, from the base up, of the following: rhyolitic and dacitic porphyritic rocks, ignimbrite, tuff, and flow. It is underlain by a pre-Jurassic basement and overlain by the hyaloclastic andesites of the Yahgán Formation. The Arroyo Rojo consists of stacked lenticular lenses that are associated with disseminated mineralization in both the footwall and the hanging wall. The internal structure of the ore lenses is marked by the occurrence of massive, semi-massive and banded facies, along with stringer and brecciated zones and minor ore disseminations. The mineral assemblage comprises mainly pyrite and sphalerite, with minor amounts of galena and chalcopyrite and rare pyrrhotite, arsenopyrite, tetrahedrite and bournonite. The ores and the volcanic host rocks have metamorphosed to greenschist facies and were overprinted by a penetrative tectonic foliation, which led to the development of mylonitic, and cataclastic textures, recrystallization and remobilization. Primary depositional characteristics and regional and hydrothermal alteration patterns were preserved despite deformation and metamorphism. Therefore, primary banding was preserved between facies boundaries. In addition, some remnants of magmatic origin are recognizable in preserved phenocrysts and volcaniclastic phenoclasts. Most of the volcanic and volcaniclastic rocks of the host sequence show a rhyolitic to rhyo-dacitic composition. Regional seafloor alteration, characterized by the presence of clinozoisite, Fe-chlorite and titanite, along with quartz and albite, is partially obliterated by hydrothermal alteration. The hydrothermal alteration is stratabound with the following assemblages, which developed from the base to top: (1) Quartz-Chlorite ± Sericite, (2) Quartz-Chlorite, (3) Chlorite ± Quartz-Sericite-Calcite, (4) Quartz-Chlorite ± Calcite and (5) Sericite + Quartz ± Chlorite ± Calcite. Magnesium-chlorite and phengitic white mica typically occur in the vicinity of the Arroyo Rojo ore lenses. To provide field criteria for exploration vectoring, the chemical composition of chlorite and the phengitic and paragonitic content of the white mica were determined and correlated with PIMA Fe-OH and Al-OH absorption wavelengths, respectively, relative to their proximity to the mineralized lenses. The results of this study can be used to help identify (1) felsic proximal facies associations, (2) ore horizons and (3) favorable hydrothermal alteration zones in other parts of the Fin del Mundo district.

Chlorite dismutases – a heme enzyme family for use in bioremediation and generation of molecular oxygen

PubMed Central

Hofbauer, Stefan; Schaffner, Irene; Furtmüller, Paul G; Obinger, Christian

2014-01-01

Chlorite is a serious environmental concern, as rising concentrations of this harmful anthropogenic compound have been detected in groundwater, drinking water, and soil. Chlorite dismutases (Clds) are therefore important molecules in bioremediation as Clds catalyze the degradation of chlorite to chloride and molecular oxygen. Clds are heme b-containing oxidoreductases present in numerous bacterial and archaeal phyla. This review presents the phylogeny of functional Clds and Cld-like proteins, and demonstrates the close relationship of this novel enzyme family to the recently discovered dye-decolorizing peroxidases. The available X-ray structures, biophysical and enzymatic properties, as well as a proposed reaction mechanism, are presented and critically discussed. Open questions about structure-function relationships are addressed, including the nature of the catalytically relevant redox and reaction intermediates and the mechanism of inactivation of Clds during turnover. Based on analysis of currently available data, chlorite dismutase from “Candidatus Nitrospira defluvii” is suggested as a model Cld for future application in biotechnology and bioremediation. Additionally, Clds can be used in various applications as local generators of molecular oxygen, a reactivity already exploited by microbes that must perform aerobic metabolic pathways in the absence of molecular oxygen. For biotechnologists in the field of chemical engineering and bioremediation, this review provides the biochemical and biophysical background of the Cld enzyme family as well as critically assesses Cld's technological potential. PMID:24519858

Genotoxicity of Swimming Pool Water and Carcinogenicity of Drinking Water

EPA Science Inventory

Among the 11 disinfection by-products (DBPs) in drinking water that are regulated by the U.S. EPA, (a) 2 DBPs (chloroaceticacid and chlorite) are not carcinogenic-in either of2 species; (b) chlorite is not carcinogenic in 3 rodent assays and has never been tested for genotoxicity...

Genotoxicity of Swimming Pool Water and Carcinogenicity of Drinking Water**

EPA Science Inventory

Among the 11 disinfection by-products (DBPs) in drinking water that are regulated by the U.S. EPA, (a) 2 DBPs (chloroaceticacid and chlorite) are not carcinogenic-in either of2 species; (b) chlorite is not carcinogenic in 3 rodent assays and has never been tested for genotoxicity...

21 CFR 173.325 - Acidified sodium chlorite solutions.

Code of Federal Regulations, 2010 CFR

2010-04-01

... 21 Food and Drugs 3 2010-04-01 2009-04-01 true Acidified sodium chlorite solutions. 173.325 Section 173.325 Food and Drugs FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES (CONTINUED) FOOD FOR HUMAN CONSUMPTION (CONTINUED) SECONDARY DIRECT FOOD ADDITIVES PERMITTED IN FOOD FOR...

OVERVIEW OF DRINKING WATER MUTAGENICITY AND CARCINOGENICITY AND RISK FOR BLADDER CANCER

EPA Science Inventory

Among the 11 disinfection by-products (DBPs) in drinking water that are regulated by the U.S. EPA, (a) 2 DBPs (chloroacetic acid and chlorite) are not carcinogenic-in either of 2 species; (b) chlorite is not carcinogenic in 3 rodent assays and has never been tested for genotoxici...

Combined effects of sodium chlorite dip treatment and chitosan coatings on the quality of fresh-cut d’Anjou pears

USDA-ARS?s Scientific Manuscript database

This study evaluated the effects of sodium chlorite (SC) alone and its sequential treatment with edible coatings on browning inhibition and quality maintenance of fresh-cut d’Anjou pears. Edible coatings were prepared from chitosan (CH) and its water soluble derivative: carboxymethyl chitosan (CMCH...

Dual effectiveness of sodium chlorite for enzymatic browning inhibition and Escherichia coli inactivation on fresh-cut apples

USDA-ARS?s Scientific Manuscript database

This study investigated the dual effectiveness of sodium chlorite (SC) for browning inhibition and microbial inactivation on fresh-cut apples. The SC treatment exhibited a strong inhibition on browning reaction of fresh-cut Red Delicious apples during cold storage. Test results from examination of t...

A case of severe chlorite poisoning successfully treated with early administration of methylene blue, renal replacement therapy, and red blood cell transfusion: case report.

PubMed

Gebhardtova, Andrea; Vavrinec, Peter; Vavrincova-Yaghi, Diana; Seelen, Mark; Dobisova, Anna; Flassikova, Zora; Cikova, Andrea; Henning, Robert H; Yaghi, Aktham

2014-08-01

The case of a 55-year-old man who attempted suicide by ingesting <100 mL of 28% sodium chlorite solution is presented. On arrival in the intensive care unit, the patient appeared cyanotic with lowered consciousness and displayed anuria and chocolate brown serum.Initial laboratory tests revealed 40% of methemoglobin. The formation of methemoglobin was effectively treated with methylene blue (10% after 29 hours).To remove the toxin, and because of the anuric acute renal failure, the patient received renal replacement therapy. Despite these therapeutic measures, the patient developed hemolytic anemia and disseminated intravascular coagulation, which were treated with red blood cell transfusion and intermittent hemodialysis. These interventions led to the improvement of his condition and the patient eventually fully recovered. Patient gave written informed consent.This is the third known case of chlorite poisoning that has been reported. Based upon this case, we suggest the management of sodium chlorite poisoning to comprise the early administration of methylene blue, in addition to renal replacement therapy and transfusion of red blood cells.

A Case of Severe Chlorite Poisoning Successfully Treated With Early Administration of Methylene Blue, Renal Replacement Therapy, and Red Blood Cell Transfusion

PubMed Central

Gebhardtova, Andrea; Vavrinec, Peter; Vavrincova-Yaghi, Diana; Seelen, Mark; Dobisova, Anna; Flassikova, Zora; Cikova, Andrea; Henning, Robert H.; Yaghi, Aktham

2014-01-01

Abstract The case of a 55-year-old man who attempted suicide by ingesting <100 mL of 28% sodium chlorite solution is presented. On arrival in the intensive care unit, the patient appeared cyanotic with lowered consciousness and displayed anuria and chocolate brown serum. Initial laboratory tests revealed 40% of methemoglobin. The formation of methemoglobin was effectively treated with methylene blue (10% after 29 hours). To remove the toxin, and because of the anuric acute renal failure, the patient received renal replacement therapy. Despite these therapeutic measures, the patient developed hemolytic anemia and disseminated intravascular coagulation, which were treated with red blood cell transfusion and intermittent hemodialysis. These interventions led to the improvement of his condition and the patient eventually fully recovered. Patient gave written informed consent. This is the third known case of chlorite poisoning that has been reported. Based upon this case, we suggest the management of sodium chlorite poisoning to comprise the early administration of methylene blue, in addition to renal replacement therapy and transfusion of red blood cells. PMID:25144325

[Study on pipe material's influence on chlorine dioxide drinking water disinfection].

PubMed

He, Tao; Yue, Yinling; Ling, Bo; Zhang, Lan

2010-09-01

To study the pipe material's influence on chlorine dioxide drinking water disinfection. 0.8 mg/L chlorine dioxide solution was injected into 5 kinds of pipes respectively, PPR, PVC-U, Steel with Zinc coating, copper and PE pipes. Dipped free from light for 48 hours and the concentrations of chlorine dioxide, chlorite and chlorate were tested from samples taken from each kind of pipe at 1, 2, 3, 4, 5, 6, 12, 24 and 48 hours respectively. Chlorine dioxides decay rates in the water dipping the pipes increase as the dipping time increases and the decay of chlorine dioxide mainly occurs within 6 hours after the dipping. But for different pipe, the influence of decay differs. The consumption of chlorine dioxide of the metal pipes is more than that of the plastic pipes. And with 2 hours after the dipping experiment begins, the concentrations of the chlorite of the copper pipe and of the steel with zinc coating pipe increase quickly and reach the maximum concentration. But then the chlorite concentration decreases greatly. After dipped 24 hours, the chlorite in the water in the pipe can not be detected. For other plastic piples, all the chlorite concentrations in the dipping water increase as the dipping time increase. Compared with the start of the dipping experiment, the chlorate concentration in the dipping water of each pipe has no obvious change. The material of the water transportation pipe does have influence on chlorine dioxide drinking water disinfection.

Evaluation of gaseous chlorine dioxide for the inactivation of Tulane virus on blueberries.

PubMed

Kingsley, David H; Pérez-Pérez, Rafael E; Niemira, Brendan A; Fan, Xuetong

2018-05-20

To determine the effectiveness of gaseous chlorine dioxide (gClO 2 ) against a human norovirus surrogate on produce, gClO 2 was generated and applied to Tulane virus-coated blueberries in a 240 ml-treatment chamber. gClO 2 was produced by an acidifying sodium chlorite solution. Initial assessments indicated that blueberries treated with gClO 2 generated from ≤1 mg acidified sodium chlorite in the small chamber appeared unaffected while gClO 2 generated from ≥10 mg of acidified sodium chlorite solution altered the appearance and quality of the blueberries. Treatments of inoculated blueberries with gClO 2 generated from 0.1 mg sodium chlorite reduced the virus populations by >1 log after exposure for 30 to 330 min. For the 1 mg sodium chlorite treatments, the virus populations were reduced by >2.2 log after 15 min exposure and to non-detectable levels (>3.3 logs reductions) after 180 min exposure. Measured concentrations of gClO 2 peaked in the treatment chamber at 0.9 μg/l after 10 min for 0.1 mg treatments and 600 μg/l after around 20 min for 1 mg treatment. Overall results indicate that gClO 2 could be a feasible waterless intervention for blueberries and other produce. Published by Elsevier B.V.

A new occurrence of ambient inclusion trails from the ~1900-million-year-old Gunflint Formation, Ontario: nanocharacterization and testing of potential formation mechanisms.

PubMed

Wacey, D; Saunders, M; Kong, C; Kilburn, M R

2016-09-01

Ambient inclusion trails (AITs) are tubular microstructures thought to form when a microscopic mineral crystal is propelled through a fine-grained rock matrix. Here, we report a new occurrence of AITs from a fossilized microbial mat within the 1878-Ma Gunflint Formation, at Current River, Ontario. The AITs are 1-15 μm in diameter, have pyrite as the propelled crystal, are infilled with chlorite and have been propelled through a microquartz (chert) or chlorite matrix. AITs most commonly originate at the boundary between pyrite- and chlorite-rich laminae and chert-filled fenestrae, with pyrite crystals propelled into the fenestrae. A subset of AITs originate within the fenestrae, rooted either within the chert or within patches of chlorite. Sulphur isotope data ((34) S/(32) S) obtained in situ from AIT pyrite have a δ(34) S of -8.5 to +8.0 ‰, indicating a maximum of ~30 ‰ fractionation from Palaeoproterozoic seawater sulphate (δ(34) S ≈ +20 ‰). Organic carbon is common both at the outer margins of the fenestrae and in patches of chlorite where most AITs originate, and can be found in smaller quantities further along some AITs towards the terminal pyrite grain. We infer that pyrite crystals now found within the AITs formed via the action of heterotrophic sulphate-reducing bacteria during early diagenesis within the microbial mat, as pore waters were becoming depleted in seawater sulphate. Gases derived from this process such as CO2 and H2 S were partially trapped within the microbial mat, helping produce birds-eye fenestrae, while rapid microquartz precipitation closed porosity. We propose that propulsion of the pyrite crystals to form AITs was driven by two complementary mechanisms during burial and low-grade metamorphism: firstly, thermal decomposition of residual organic material providing CO2 , and potentially CH4 , as propulsive gases, plus organic acids to locally dissolve the microquartz matrix; and secondly, reactions involving clay minerals that potentially led to enhanced quartz solubility, plus increases in fluid and/or gas pressure during chlorite formation, with chlorite then infilling the AITs. This latter mechanism is novel and represents a possible way to generate AITs in environments lacking organic material. © 2016 John Wiley & Sons Ltd.

Combination of sodium chlorite and calcium propionate reduces enzymatic browning and microbial population of fresh-cut ‘Granny Smith’ apples

USDA-ARS?s Scientific Manuscript database

Tissue browning and microbial growth are the main concerns associated with fresh-cut apples. In this study, effects of sodium chlorite (SC) and calcium propionate (CP), individually and combined, on quality and microbial population of apple slices were investigated. ‘Granny Smith’ apple slices, dipp...

Polyacetal Carboxylic Acids: a New Group of Antiviral Polyanions

PubMed Central

Claes, P.; Billiau, A.; De Clercq, E.; Desmyter, J.; Schonne, E.; Vanderhaeghe, H.; De Somer, P.

1970-01-01

Chlorite-oxidized oxypolysaccharides are polyacetal carboxylic acids. They inhibited the cytopathic effect of vesicular stomatitis virus in mouse embryo cell cultures challenged at low input multiplicity. After intraperitoneal injection of these compounds in mice, interferon appeared in the circulation. The compounds also protected mice against lethal mengovirus infection and against the development of experimental pox lesions on the tail. Chlorite-oxidized oxyamylose was antiviral only when at least 64% of the glucopyranose units were oxidized, an observation which suggested a correlation between charge density and antiviral effect. The antiviral activity was also influenced by the molecular weight, as demonstrated by the fact that chlorite-oxidized dextrans which had a high intrinsic viscosity were more active than those with low intrinsic viscosity. PMID:4314553

Groups at potentially high risk from chlorine dioxide treated water.

PubMed

Moore, G S; Calabrese, E J; Ho, S C

1980-09-01

Chlorite, a by-product of chlorine dioxide disinfection of water, is a strong oxidant compound that produces markedly exaggerated effects in vitro on red cells of G6PD deficient humans when compared to normal human cells. Levels of methemoglobin are significantly greater and GSH levels significantly lower in the G6PD deficient cells than in normal cells after chlorite exposure. Persons with G6PD deficiency may be 3 to 4 times more likely to develop hemolytic anemia from chlorite exposure as persons with normal activity levels when GSH levels are used as a measure of susceptibility. The proposed use of chlorine dioxide as an alternate disinfectant for drinking water supplies should consider this potential high risk group.

Genesis and significance of the silico-aluminous nodules in the Ordovician of the Montagne Noire and the Massif Armoricain (France)

NASA Astrophysics Data System (ADS)

Becq-Giraudon, Jean-François; Bouillé, Suzanne; Chauvel, Jean-Jacques

1992-04-01

Siliceous nodules of the Arenigian of the Montagne Noire (southern France) and the Massif Armoricain (western France) are made up of quartz, illite and chlorite with secondary apatite and, less frequently, dolomite. Diffractometrical and geochemical data indicate that the chlorite is a chamosite (trioctahedral 2:1 chlorite), whose development may be accompanied by that of apatite and diminution of illite. Three types of nodules are defined: Type 1, siliceous nodules, with more than 85% of SiO 2, very frequent in the Montagne Noire; Type II, nodules made of a micaceous siltstone with chlorite matrix, abundant in the Massif Armoricain but present also in the Montagne Noire; Type III, chloritic nodules with a finely globular structure, especially developed in the Massif armoricain but observed in the Montagne Noire as well. The nodules are always poorer in illite than their host sediments and often show traces of the initial sediments. Their formation occurs after the deposition and prior to the development of foliation. The frequent presence of undistorted fossil remains suggests an early formation linked to the physico-chemical modifications occurring in an unconsolidated sediment around a decaying organism. The post-depositional mineralogical evolution should have started with an illite/dolomite assemblage and end up with a chamosite-dominant one, under cold climatic conditions. The simultaneous presence of the three types of nodules in the same formation, or even in the same beds, shows that this mineralogical differentiation is not strictly related to the diagenetic and metamorphic transformation of this material.

Influence of drinking water treatments on chlorine dioxide consumption and chlorite/chlorate formation.

PubMed

Sorlini, Sabrina; Gialdini, Francesca; Biasibetti, Michela; Collivignarelli, Carlo

2014-05-01

Disinfection is the last treatment stage of a Drinking Water Treatment Plant (DWTP) and is carried out to maintain a residual concentration of disinfectant in the water distribution system. Chlorine dioxide (ClO2) is a widely used chemical employed for this purpose. The aim of this work was to evaluate the influence of several treatments on chlorine dioxide consumption and on chlorite and chlorate formation in the final oxidation/disinfection stage. A number of tests was performed at laboratory scale employing water samples collected from the DWTP of Cremona (Italy). The following processes were studied: oxidation with potassium permanganate, chlorine dioxide and sodium hypochlorite, coagulation/flocculation with ferric chloride and aluminum sulfate, filtration and adsorption onto activated carbon. The results showed that the chlorine dioxide demand is high if sodium hypochlorite or potassium permanganate are employed in pre-oxidation. On the other hand, chlorine dioxide leads to the highest production of chlorite and chlorate. The coagulation/flocculation process after pre-oxidation shows that chlorine dioxide demand decreases if potassium permanganate is employed as an oxidant, both with ferric chloride and aluminum sulfate. Therefore, the combination of these processes leads to a lower production of chlorite and chlorate. Aluminum sulfate is preferable in terms of the chlorine dioxide demand reduction and minimization of the chlorite and chlorate formation. Activated carbon is the most effective solution as it reduced the chlorine dioxide consumption by about 50% and the DBP formation by about 20-40%. Copyright © 2014 Elsevier Ltd. All rights reserved.

HP LT Variscan metamorphism in the Cubito-Moura schists (Ossa-Morena Zone, southern Iberia)

NASA Astrophysics Data System (ADS)

Booth-Rea, Guillermo; Simancas, José Fernando; Azor, Antonio; Azañón, José Miguel; González-Lodeiro, Francisco; Fonseca, Paulo

2006-12-01

Multi-equilibrium thermobarometry shows that low-grade metapelites (Cubito-Moura schists) from the Ossa-Morena Zone underwent HP-LT metamorphism from 340-370 °C at 1.0-0.9 GPa to 400-450 °C at 0.8-0.7 GPa. These HP-LT equilibriums were reached by parageneses including white K mica, chlorite and chloritoid, which define the earliest schistosity (S 1) in these rocks. The main foliation in the schists is a crenulation cleavage (S 2), which developed during decompression from 0.8-0.7 to 0.4-0.3 GPa at increasing temperatures from 400-450 °C to 440-465 °C. Fe 3+ in chlorite decreased greatly during prograde metamorphism from molar fractions of 0.4 determined in syn-S 1 chlorites down to 0.1 in syn-S 2 chlorites. These new data add to previous findings of eclogites in the Moura schists indicating that a pile of allochtonous rocks situated next to the Beja-Acebuches oceanic amphibolites underwent HP-LT metamorphism during the Variscan orogeny. To cite this article: G. Booth-Rea et al., C. R. Geoscience 338 (2006).

Estimating the Mg# and AlVI content of biotite and chlorite from shortwave infrared reflectance spectroscopy: Predictive equations and recommendations for their use

NASA Astrophysics Data System (ADS)

Lypaczewski, Philip; Rivard, Benoit

2018-06-01

Shortwave infrared (SWIR, 1000-2500 nm) reflectance spectra of biotite and chlorite were investigated to establish quantitative relationships between spectral metrics and mineral chemistry, determined by electron microprobe analysis (EMPA). Samples spanning a broad range of mineral compositions were used to establish regression equations to Mg#, which can be estimated to ±3 and ±5 Mg#, and to AlVI content, which can be estimated to ±0.044 AlVI (11 O) and ±0.09 AlVI (14 O), respectively for biotite and chlorite. Both minerals have absorptions at common positions (1400, 2250, 2330 nm), and spectral interference may occur in mineral mixtures. For an equivalent Mg#, absorptions of chlorite are offset to 1-15 nm higher wavelengths relative to those of biotite. If the incorrect mineral is identified, errors in the estimation of composition may occur. Additionally, the 2250 nm absorption, which is related to Al(Mg,Fe)-OH in both minerals, is strongly affected by both the AlVI content and Mg#. This can lead to erroneous Mg# estimations in low AlVI samples. Recommendations to mitigate these issues are presented.

Low grade metamorphism fluid circulation in a sedimentary environment thrust fault zone: properties and modeling

NASA Astrophysics Data System (ADS)

Trincal, Vincent; Lacroix, Brice; Buatier, Martine D.; Charpentier, Delphine; Labaume, Pierre; Lahfid, Abdeltif

2014-05-01

In fold-and-thrust belts, shortening is mainly accommodated by thrust faults that can constitute preferential pathways for fluid circulation. The present study focuses on the Pic de Port Vieux thrust, a second-order thrust related to major Gavarnie thrust in the Axial Zone of the Pyrenees. The fault juxtaposes lower Triassic red siltstones and sandstones in the hanging-wall and Upper Cretaceous limestone in the footwall. A dense network of synkinematic quartz-chlorite veins is present in outcrop and allows to unravel the nature of the fluid that circulated in the fault zone. The hanging wall part of fault zone comprises a core which consists of intensely foliated phyllonite; the green color of this shear zone is related to the presence of abundant newly-formed chlorite. Above, the damage zone consists of red pelites and sandstones. Both domains feature kinematic markers like S-C type shear structures associated with shear and extension quartz-chlorite veins and indicate a top to the south displacement. In the footwall, the limestone display increasing mylonitization and marmorization when getting close to the contact. In order to investigate the mineralogical and geochemical changes induced by deformation and subsequent fluid flow, sampling was conducted along a complete transect of the fault zone, from the footwall limestone to the red pelites of the hanging wall. In the footwall limestone, stable isotope and Raman spectroscopy analyzes were performed. The strain gradient is strongly correlated with a high decrease in δ18OV PDB values (from -5.5 to -14) when approaching the thrust (i.e. passing from limestone to marble) while the deformation temperatures estimated with Raman spectroscopy on carbon remain constant around 300° C. These results suggest that deformation is associated to a dynamic calcite recrystallization of carbonate in a fluid-open system. In the hanging wall, SEM observations, bulk chemical XRF analyses and mineral quantification from XRD analyses were conducted in order to compare the green phyllonites from the fault core zone with the red pelites from the damage zone. Quartz, muscovite 2M1, chlorite (clinochlore), calcite and rutile are present in all samples. Hematite occurs in the damage zone but is absent in the core zone. Synkinematic chlorites are abundant in the core and damage zones and are mainly located in veins, sometimes in association with quartz. The temperature of formation of these newly-formed chlorites is 300-350° C according to Inoue (2009) geothermometer. Mössbauer spectroscopic analyses were performed on bulk rock samples. In the damage zone, Fe3+/Fetotal vary between 0.7 and 0.8, whereas in the core zone Fe3+/Fetotal is about 0.35. This decrease in Fe3+ from the damage zone to the core zone can be related to the dissolution of hematite. In contrast, Fe3+/Fetotal in phyllosilicates is clearly related to the chlorite content relative to mica, as Fe2+ increases with chlorite content. All these data allow us to propose a model of fluid circulation in relation with the Pic de Port Vieux thrust activity. The origin of the fluid, its interactions with host-rock and the consequences on fault zone mineralizations will be discussed. Inoue, A., Meunier, A., Patrier-Mas, P., Rigault, C., Beaufort, D., Vieillard, P., 2009. Application of chemical geothermometry to low-temperature trioctahedral chlorites. Clay Clay Min. 57, 371-382.

Boron isotope fractionation during high-pressure dehydration of antigorite serpentinite

NASA Astrophysics Data System (ADS)

Harvey, J.; Garrido, C.; Agostini, S.; Padron Navarta, J.; López Sánchez-Vizcaíno, V.; Savov, I. P.; Marchesi, C.

2011-12-01

During subduction, antigorite-serpentinite is present in large volumes in both the downgoing slab and the overlying mantle wedge. There is strong evidence to suggest that deserpentinisation reactions are a source for several fluid mobile elements, including boron. The ultramafic rocks of Cerro del Almirez, Betic Cordillera, Spain are the only known outcrops that preserve evidence for the transition between antigorite-serpentinite and chlorite-harzburgite i.e., Almirez antigorite-serpentinite represents an early stage of prograde subduction zone metamorphism overprinting previously hydrated oceanic mantle. The stability of chlorite beyond the antigorite breakdown reaction limits the release of H2O to about 6-7 wt% (in the absence of chlorite up to 12 wt% H2O would be lost), i.e. the reaction at the antigorite-serpentinite / chlorite harzburgite front is a dehydration reaction which may fractionate boron isotopes because of the mineralogical change, because of the loss of fluid over a range of temperatures, or a combination of both. Although the behaviour of boron isotopes under closely controlled experimental conditions with a limited number of variables is reasonably well constrained, the mechanism or combination of mechanisms that fractionate 11B from 10B in natural samples can be complex and difficult to interpret, especially in samples of the sub-arc mantle wedge which is seldom accessible for direct examination. This study investigates the influence of dehydration reactions in the sub-arc region where fluid loss accompanies prograde metamorphism under well constrained pressure and temperature conditions. Initial results suggest that isotopes of boron are strongly fractionated during the dehydration of antigorite-serpentinite with marked differences in δ11B across the antigorite-serpentinite to chlorite-harzburgite isograd. Antigorite-serpentinite has a δ11B of +22.4 (± 0.9) whereas the dehydration reaction product, chlorite-harzburgite, has a δ11B ranging from +2.7 (± 0.4) to -3.5 (± 0.3). A single sample with a transitional antigorite-chlorite serpentinite lithology, taken from as near to the isograd as possible, preserves a δ11B of +3.3 (± 0.3). This suggests that a substantial proportion of fluid loss, and therefore the potential fractionation of boron isotopes, occurs early on in the prograde reaction - the largest changes in δ11B occurring between antigorite-serpentinite and the transitional lithology, while the prograde lithology preserves a narrower, yet still markedly heterogeneous range of δ11B. This suggests that dehydration of serpentinite results in a strong fractionation of boron isotopes and that the results of the dehydration reaction survive high P-T condition (650 °C, 1.7 GPa). Moreover, this may also indicate that a chlorite-hosted, B-rich reservoir with a heterogeneous δ11B can persist in the lithospheric mantle elsewhere and may modify basaltic melts with which it interacts.

Higher acid-chlorite reactivity of cell corner middle lamella lignin in black spruce

Treesearch

Umesh P. Agarwal

2007-01-01

To determine if there was a delignification behavior difference between secondary wall (S2) and middle lamella (cell corner or CC) lignin, black spruce cross-sections were acid-chlorite delignified and the tissue was evaluated in-situ by Raman imaging. Lignin concentration in S2 and CC was determined in numerous latewood cell areas in the two hour delignified cross...

Pore water evolution in sandstones of the Groundhog Coalfield, northern Bowser Basin, British Columbia

NASA Astrophysics Data System (ADS)

Cookenboo, H. O.; Bustin, R. M.

1999-01-01

The succession of sandstone cements in chert and volcanic lithic arenites and wackes from the northern Bowser Basin of British Columbia comprises a record of diagenesis in shallow marine, deltaic, and coastal plain siliciclastic sediments that pass through the oil window and reach temperatures near the onset of metamorphism. The succession of cements is consistent with seawater in the sandstones mixing with acid waters derived from dewatering of interbedded organic rich muds. Sandstone cement paragenesis includes seven discrete cement stages. From earliest to latest the cement stages are: (1) pore-lining chlorite; (2) pore-lining to pore-filling illite; (3) pore-filling kaolinite; (4) oil migration through some of the remaining connected pores; (5) chlorite dissolution; (6) quartz cement; and (7) calcite cement. These seven cement stages are interpreted as a record of the evolution of pore waters circulating through the sandstones after burial. The earliest cement stages, as well as the depositional environments, are compatible with seawater as the initial pore fluid. Seawater composition changed during transport through the sandstones, first by loss of Mg 2+ and Fe 2+ during chlorite precipitation (stage 1). Dewatering of interbedded organic-rich mudstones probably added Mg 2+ and Fe 2+ to partially buffer the loss of these cations to chlorite. Acids produced during breakdown of organic matter are presumed to have mixed into sandstone pore fluids due to further compaction of the muds, leading to reduction of initial alkalinity. Reduction in alkalinity, in turn, favours change from chlorite to illite precipitation (stage 2), and finally to kaolinite (stage 3). Pore waters likely reached their peak acidity at the time of oil migration (stage 4). Chlorite dissolution (stage 5) and quartz precipitation (stage 6) occurred when pores were filled by these hydrocarbon-bearing and presumably acidic fluids. Fluid inclusions in fracture-filling quartz cements contain petroleum, high-pressure methane, and methane-rich aqueous solutions. Homogenization temperatures from primary two-phase inclusions are consistent with quartz cementation during progressive heating between approximately 100 and 200°C. Following quartz precipitation, alkaline pore waters were re-established, as evidenced by late-stage calcite cement (stage 7).

Manipulating Conserved Heme Cavity Residues of Chlorite Dismutase: Effect on Structure, Redox Chemistry, and Reactivity

PubMed Central

2013-01-01

Chlorite dismutases (Clds) are heme b containing oxidoreductases that convert chlorite to chloride and molecular oxygen. In order to elucidate the role of conserved heme cavity residues in the catalysis of this reaction comprehensive mutational and biochemical analyses of Cld from “Candidatus Nitrospira defluvii” (NdCld) were performed. Particularly, point mutations of the cavity-forming residues R173, K141, W145, W146, and E210 were performed. The effect of manipulation in 12 single and double mutants was probed by UV–vis spectroscopy, spectroelectrochemistry, pre-steady-state and steady-state kinetics, and X-ray crystallography. Resulting biochemical data are discussed with respect to the known crystal structure of wild-type NdCld and the variants R173A and R173K as well as the structures of R173E, W145V, W145F, and the R173Q/W146Y solved in this work. The findings allow a critical analysis of the role of these heme cavity residues in the reaction mechanism of chlorite degradation that is proposed to involve hypohalous acid as transient intermediate and formation of an O=O bond. The distal R173 is shown to be important (but not fully essential) for the reaction with chlorite, and, upon addition of cyanide, it acts as a proton acceptor in the formation of the resulting low-spin complex. The proximal H-bonding network including K141-E210-H160 keeps the enzyme in its ferric (E°′ = −113 mV) and mainly five-coordinated high-spin state and is very susceptible to perturbation. PMID:24364531

Thermodynamic properties of chlorite and berthierine derived from calorimetric measurements

NASA Astrophysics Data System (ADS)

Blanc, Philippe; Gailhanou, Hélène; Rogez, Jacques; Mikaelian, Georges; Kawaji, Hitoshi; Warmont, Fabienne; Gaboreau, Stéphane; Grangeon, Sylvain; Grenèche, Jean-Marc; Vieillard, Philippe; Fialips, Claire I.; Giffaut, Eric; Gaucher, Eric C.; Claret, F.

2014-09-01

In the context of the deep waste disposal, we have investigated the respective stabilities of two iron-bearing clay minerals: berthierine ISGS from Illinois [USA; (Al0.975FeIII0.182FeII1.422Mg0.157Li0.035Mn0.002)(Si1.332Al0.668)O5(OH)4] and chlorite CCa-2 from Flagstaff Hill, California [USA; (Si2.633Al1.367)(Al1.116FeIII0.215Mg2.952FeII1.712Mn0.012Ca0.011)O10(OH)8]. For berthierine, the complete thermodynamic dataset was determined at 1 bar and from 2 to 310 K, using calorimetric methods. The standard enthalpies of formation were obtained by solution-reaction calorimetry at 298.15 K, and the heat capacities were measured by heat-pulse calorimetry. For chlorite, the standard enthalpy of formation is measured by solution-reaction calorimetry at 298.15 K. This is completing the entropy and heat capacity obtained previously by Gailhanou et al. (Geochim Cosmochim Acta 73:4738-4749, 2009) between 2 and 520 K, by using low-temperature adiabatic calorimetry and differential scanning calorimetry. For both minerals, the standard entropies and the Gibbs free energies of formation at 298.15 K were then calculated. An assessment of the measured properties could be carried out with respect to literature data. Eventually, the thermodynamic dataset allowed realizing theoretical calculations concerning the berthierine to chlorite transition. The latter showed that, from a thermodynamic viewpoint, the main factor controlling this transition is probably the composition of the berthierine and chlorite minerals and the nature of the secondary minerals rather than temperature.

Acid--chlorite pretreatment and liquefaction of cornstalk in hot-compressed water for bio-oil production.

PubMed

Liu, Hua-Min; Feng, Bing; Sun, Run-Cang

2011-10-12

In this study, cornstalk was pretreated by an acid-chlorite delignification procedure to enhance the conversion of cornstalk to bio-oil in hot-compressed water liquefaction. The effects of the pretreatment conditions on the compositional and structural changes of the cornstalk and bio-oil yield were investigated. It was found that acid-chlorite pretreatment changed the main components and physical structures of cornstalk and effectively enhanced the bio-oil yield. Shorter residence time favored production of the total bio-oil products, whereas longer time led to cracking of the products. A high water loading was found to be favorable for high yields of total bio-oil and water-soluble oil. GC-MS analysis showed that the water-soluble oil and heavy oil were the complicated products of C(5-10) and C(8-11) organic compounds.

EVALUATION OF THE IMMUNOMODULATORY EFFECTS OF THE DISINFECTION BYPRODUCT, SODIUM CHLORITE, IN FEMALE B6C3F1 MICE: A DRINKING WATER STUDY

EPA Science Inventory

Evaluation of the Immunomodulatory Effects of the Disinfection By-product, Sodium chlorite, in Female B6C3f1 mice: A Drinking Water Study.

Niel A. Karrow, Tal, L. Guo, J. Ann McCay, Greg W. Johnson, Ronnetta D. Brown, Debrorah L. Musgrove, Dori R. Germolec, Robert W. Lueb...

Redox Thermodynamics of High-Spin and Low-Spin Forms of Chlorite Dismutases with Diverse Subunit and Oligomeric Structures

PubMed Central

2012-01-01

Chlorite dismutases (Clds) are heme b-containing oxidoreductases that convert chlorite to chloride and dioxygen. In this work, the thermodynamics of the one-electron reduction of the ferric high-spin forms and of the six-coordinate low-spin cyanide adducts of the enzymes from Nitrobacter winogradskyi (NwCld) and Candidatus “Nitrospira defluvii” (NdCld) were determined through spectroelectrochemical experiments. These proteins belong to two phylogenetically separated lineages that differ in subunit (21.5 and 26 kDa, respectively) and oligomeric (dimeric and pentameric, respectively) structure but exhibit similar chlorite degradation activity. The E°′ values for free and cyanide-bound proteins were determined to be −119 and −397 mV for NwCld and −113 and −404 mV for NdCld, respectively (pH 7.0, 25 °C). Variable-temperature spectroelectrochemical experiments revealed that the oxidized state of both proteins is enthalpically stabilized. Molecular dynamics simulations suggest that changes in the protein structure are negligible, whereas solvent reorganization is mainly responsible for the increase in entropy during the redox reaction. Obtained data are discussed with respect to the known structures of the two Clds and the proposed reaction mechanism. PMID:23126649

The Effect of Treatment with Hydrogen Peroxide and the Mehra-Jackson Reagent on X-ray Diffraction Patterns of Clay Fractions

NASA Astrophysics Data System (ADS)

Sokolova, T. A.; Tolpeshta, I. I.; Izosimova, Yu. G.; Umnova, V. A.; Lashukov, P. V.

2017-12-01

X-ray diffraction patterns of clay fractions from the AEL and EL horizons of pale-podzolic soil before and after treatment with 10% H2O2 and the Mehra-Jackson reagent in different sequences have been examined. The successive treatment with 10% H2O2 and then with the Mehra-Jackson reagent causes dissolution of Al-hydroxy-interlayers in pedogenic chlorites and the respective increase in the content of labile minerals because of a dramatic decrease in pH upon the treatment with hydrogen peroxide. The rate of these changes depends on the degree of chloritization of pedogenic chlorites in the initial samples. The result of the reverse sequence of the treatments of clay fractions (initially with the Mehra-Jackson reagent and then with hydrogen peroxide) is opposite: the chloritization of labile minerals becomes more intensive. It is provided by pH values that do not drop below 7.5 at any treatment stage. At particular stages, pH values favors the mobilization of Al compounds and their subsequent polymerization in the interlayer space of labile structures. We suppose that hydroxyl-aluminosilicate layers may be formed in the interlayer space upon this treatment sequence.

Controlled Release of Antimicrobial ClO2 Gas from a Two-Layer Polymeric Film System.

PubMed

Bai, Zhifeng; Cristancho, Diego E; Rachford, Aaron A; Reder, Amy L; Williamson, Alexander; Grzesiak, Adam L

2016-11-16

We report a two-component label system comprising a chlorite-containing polymer film and an acid-containing polymer film that can release antimicrobial ClO 2 gas upon adhering the two films together to enable a reaction of the chlorite and acid under moisture exposure. The chlorite-containing film comprises a commercial acrylate-based pressure-sensitive adhesive polymer impregnated with sodium chlorite. The acid-containing film comprises a commercial poly(vinyl alcohol) polymer loaded with tartaric acid. Both of the films were prepared on low ClO 2 -absorbing substrate films from stable aqueous systems of the polymers with high reagent loading. Rapid and sustained releases of significant amounts of ClO 2 gas from the label system were observed in an in situ quantification system using UV-vis spectroscopy. It was found that the ClO 2 release is slower at a lower temperature and can be accelerated by moisture in the atmosphere and the films. Controlled release of ClO 2 gas from the label system was demonstrated by tailoring film composition and thickness. A model was developed to extract release kinetics and revealed good conversions of the label system. This two-component system can potentially be applied as a two-part label without premature release for applications in food packaging.

Surface energy of talc and chlorite: Comparison between electronegativity calculation and immersion results.

PubMed

Douillard, Jean-Marc; Salles, Fabrice; Henry, Marc; Malandrini, Harold; Clauss, Frédéric

2007-01-15

The surface energies of talc and chlorite is computed using a simple model, which uses the calculation of the electrostatic energy of the crystal. It is necessary to calculate the atomic charges. We have chosen to follow Henry's model of determination of partial charges using scales of electronegativity and hardness. The results are in correct agreement with a determination of the surface energy obtained from an analysis of the heat of immersion data. Both results indicate that the surface energy of talc is lower than the surface energy of chlorite, in agreement with observed behavior of wettability. The influence of Al and Fe on this phenomenon is discussed. Surface energy of this type of solids seems to depend more strongly on the geometry of the crystal than on the type of atoms pointing out of the surface; i.e., the surface energy depends more on the physics of the system than on its chemistry.

Cycling of Volatiles and Stable Isotopes During High-P Subduction Dehydration of Serpentinite

NASA Astrophysics Data System (ADS)

Alt, J.; Garrido, C. J.; Shanks, W. C.; Turchyn, A. V.; López-Sánchez-Vizcaíno, V.; Gómez-Pugnaire, M.

2009-12-01

We present volatile contents and stable isotope compositions of high-P antigorite serpentinites and their chlorite-harzburgite dehydration products from the Cerro del Almirez complex, Spain. The serpentinites are former Tethyan seafoor consisting of antigorite with olivine, diopside, chlorite, magnetite, tremolite, and Ti-clinohumite, dehydrated to chlorite-harzburites comprising spinifex-like olivine + orthopyroxene, with chlorite, tremolite, and magnetite, at T> 650°C and P>2 GPa. The serpentinites have elevated H2O, S, and C contents, averaging (n=10) 1000 ppm S and 10 wt% H2O, and with 180-1280 ppm total C. Bulk δ18O values of 7.9-9.1‰ and δD= -49 to -61‰ are consistent with serpentinization by seawater at 50-100°C. The high sulfide contents and preliminary δ34S analyses of ~10‰ likely reflect microbial reduction of seawater sulfate, and δ13C (total C) values of -10.9 to -20.2‰ are consistent with the presence of an organic carbon component. These data and processes are similar to those for modern seafloor serpentinites. High-P dehydration of the serpentinites resulted in loss of about half of their H2O and S: chlorite-harzburgites (n=11) average 5.7 wt% H2O and 610 ppm S. The δ34S (-5.1 to 10.2‰) and δ18O (6.4-9.5‰) of the metamorphic harzburgites are unchanged from serpentinite, but hydrogen isotopes are fractionated during dehydration, from serpentinite δD values around -55‰ to chlorite-harzburgite values of ~ -70 to -90‰. Carbon contents and δ13C values of the two rock types overlap, with a broad trend of decreasing C contents and δ13C, from ~1200 to 200 ppm and -9.6 to -20.3‰, perhaps reflecting loss of CO2. Our results indicate: 1) significant uptake of H2O, S and C during serpentinization on the seafloor; 2) that recycling of serpentinites to high P and T results in loss of isotopically fractionated sulfur, water and possibly carbon to the sub-arc mantle; and 3) that fractionated sulfur, water and carbon in serpentinite dehydration products can be recycled into the mantle where they can contribute to isotope heterogeneities.

How active site protonation state influences the reactivity and ligation of the heme in chlorite dismutase

PubMed Central

Streit, Bennett R.; Blanc, Béatrice; Lukat-Rodgers, Gudrun S.; Rodgers, Kenton R.; DuBois, Jennifer L.

2010-01-01

Chlorite dismutase catalyzes O2 release from chlorite with exquisite efficiency and specificity. The spectroscopic properties, ligand binding affinities, and steady state kinetics of chlorite dismutase from Dechloromonas aromatica were examined over pH 3–11.5 to gain insight into how the protonation state of the heme environment influences dioxygen formation. An acid/base transition was observed by UV/visible and resonance Raman spectroscopy with a pKa of 8.7, 2–3 pH units below analogous transitions observed in typical His-ligated peroxidases. This transition marks the conversion of a five coordinate high spin Fe(III) to a mixed high/low spin ferric-hydroxide, as confirmed by resonance Raman (rR) spectroscopy. The two Fe–OH stretching frequencies are quite low, consistent with a weak Fe–OH bond, despite the nearly neutral imidazole side chain of the proximal histidine ligand. The hydroxide is proposed to interact strongly with a distal H-bond donor, thereby weakening the Fe–OH bond. The rR spectra of Cld-CO as a function of pH reveal two forms of the complex, one in which there is minimal interaction of distal residues with the carbonyl oxygen and another, acidic form in which the oxygen is under the influence of positive charge. Recent crystallographic data reveal arginine 183 as the lone H-bond donating residue in the distal pocket. It is likely that this Arg is the strong, positively charged H-bond donor implicated by vibrational data to interact with exogenous axial heme ligands. The same Arg in its neutral (pKa ~ 6.5) form also appears to act as the active site base in binding reactions of protonated ligands, such as HCN, to ferric Cld. The steady state profile for the rate of chlorite decomposition is characterized by these same pKas. The 5 coordinate high spin acidic Cld is more active than the alkaline hydroxide-bound form. The acid form decomposes chlorite most efficiently when the distal Arg is protonated/cationic (maximum kcat = 2.0 (±0.6) × 105 s−1, kcat/KM = 3.2 (±0.4) × 107 M−1s−1, pH 5.2, 4 °C) and to a somewhat lesser extent when it acts as a H-bond donor to the axial hydroxide ligand under alkaline conditions. PMID:20356038

Geochemical signatures of copper redistribution in IOCG-type mineralisation, Gawler Craton, South Australia

NASA Astrophysics Data System (ADS)

Uvarova, Yulia A.; Pearce, Mark A.; Liu, Weihua; Cleverley, James S.; Hough, Robert M.

2018-04-01

The Emmie Bluff iron oxide, copper, gold (IOCG) prospect is located in the Olympic Dam district, South Australia, and hosts sub-economic 150-m-thick Cu-Au mineralisation associated with the hematite-chlorite-sericite alteration with chalcopyrite commonly replacing pre-existing pyrite at a depth of 800 m. With the use of cutting-edge synchrotron X-ray fluorescence microscopy and field emission gun-scanning electron microscopy, it is shown for the first time that sub-economic IOCG mineralisation in the Olympic Dam district was affected by a late fluid event, which resulted in partial dissolution of Cu mineralisation and transport of Cu in the form of chloride complexes. The porous chlorite-sericite matrix associated with the late alteration of chalcopyrite hosts a Cu-Cl-OH phase previously undescribed in IOCG rocks, which was identified as one of the polymorphs of the atacamite group of minerals, Cu2Cl(OH)3. Thermodynamic modelling shows that "atacamite" is produced during dissolution of chalcopyrite by an oxidised, Cl-bearing fluid. An acidic environment is produced within millimetres of the chalcopyrite grains during oxidation. This process drives chlorite recrystallisation that is recorded by compositional variation of chlorite proximal to chalcopyrite. The existence of the atacamite is discussed in the context of fluid evolution and interaction with IOCG-type mineralisation and its implications to ore preservation versus destruction and remobilisation.

Microtectonic-assisted P-T determination on low-grade Alpine metamorphic rocks from the "Tisia Mega-Unit" of the Slavonian Mountains in Croatia

NASA Astrophysics Data System (ADS)

Balen, Dražen; Lihter, Iva; Massonne, Hans-Joachim

2016-04-01

The internal structure of the Tisia (Tisza) Mega-Unit in the Alpine-Carpathian-Dinaridic orogenic system encompasses large Alpine nappe systems brought to its present-day position by complex regional-scale movements. The Slavonian Mountains are part of the Bihor nappe system which is below the Codru and above the Mecsek nappe systems. The low-grade metamorphic schist unit of the Slavonian Mountains includes numerous rocks which were previously related to Precambrian and/or Lower Paleozoic orogeneses. However, recent studies (e.g. Balen, 2014, European Geosciences Union General Assembly, EGU 2014-6122) show that the metapelites of this unit should be attributed to the Alpine orogeny and the poorly known P-T conditions, which they experienced, should be refined. Although metapelites can be sensitive to changes of metamorphic conditions and, therefore, be suitable for the P-T estimation of metamorphic event(s), the extraction of mineral assemblages, being in equilibrium, and associated microtectonic data for particular low-grade metamorphic rocks is not straightforward. On the contrary, due to lack of suitable minerals and complex mictotectonic features, one can be faced with a severe problem concerning (dis)equilibrium. To avoid this, the observation scale in the research was set to the sub-mm level taking into account microtectonic positions of minerals. The investigated samples from the Slavonian Mountains are fine-grained schists consisting of chlorite (15-30 vol. %), white mica (15-25 vol. %), quartz (10-25 vol. %), feldspars (albite 10-15 vol. %; some K-feldspar), biotite (<5 vol. %), opaques (<5 vol. %), and accessory minerals (zircon, monazite, xenotime, apatite, chalcopyrite, pyrite, barite, parisite-(Ce), rutile). The schists show complex microtectonic fabric including well-developed foliations, pervasive folding, crenulation and cleavage. Foliations are defined by the preferred orientation of phyllosilicates and thin quartz and feldspar ribbons. Chlorite and white mica oriented along the S1 foliation are up to 50 μm long grains whereas those oriented along the S2 foliation are as large as 500 μm. Chlorite is ripidolite; potassic white mica is muscovite to phengite. Both minerals show a systematic variation in chemical composition such as higher Si contents in white mica and lower XFe in chlorite of the S1 assemblage compared to the S2 assemblage. The application of classical chlorite thermometers, based on Si, Al, Fe, and Mg contents of chlorite, and phengite gave P-T conditions of 325-350 °C around 4.6 kbar and 315-330 °C around 3.8 kbar for the S1 and S2 minerals, respectively. Constructions of pseudosections in the system MnNCKFMASHTO with PERPLEX confirmed these P-T ranges yielding 3.1-4.7 kbar and 300-360 °C based on intersections of XFe (chlorite) and Si (phengite) isopleths. The P-T range is in accordance with the critical reaction chlorite + K-feldspar = biotite + K-white mica in the presence of quartz and H2O. The presented refinement of the P-T data for the studied metapelites combined with two sets of known monazite ages (113±20 and 82±23 Ma; Balen, 2014) has a significance in clarifying details of the geodynamic evolution during the Alpine orogeny. Financial support by the Croatian Science Foundation (IP-2014-09-9541) and T. Theye's help during microprobe work is greatly acknowledged.

Microscale mapping of alteration conditions and potential biosignatures in basaltic-ultramafic rocks on early Earth and beyond.

PubMed

Grosch, Eugene G; McLoughlin, Nicola; Lanari, Pierre; Erambert, Muriel; Vidal, Olivier

2014-03-01

Subseafloor environments preserved in Archean greenstone belts provide an analogue for investigating potential subsurface habitats on Mars. The c. 3.5-3.4 Ga pillow lava metabasalts of the mid-Archean Barberton greenstone belt, South Africa, have been argued to contain the earliest evidence for microbial subseafloor life. This includes candidate trace fossils in the form of titanite microtextures, and sulfur isotopic signatures of pyrite preserved in metabasaltic glass of the c. 3.472 Ga Hooggenoeg Formation. It has been contended that similar microtextures in altered martian basalts may represent potential extraterrestrial biosignatures of microbe-fluid-rock interaction. But despite numerous studies describing these putative early traces of life, a detailed metamorphic characterization of the microtextures and their host alteration conditions in the ancient pillow lava metabasites is lacking. Here, we present a new nondestructive technique with which to study the in situ metamorphic alteration conditions associated with potential biosignatures in mafic-ultramafic rocks of the Hooggenoeg Formation. Our approach combines quantitative microscale compositional mapping by electron microprobe with inverse thermodynamic modeling to derive low-temperature chlorite crystallization conditions. We found that the titanite microtextures formed under subgreenschist to greenschist facies conditions. Two chlorite temperature groups were identified in the maps surrounding the titanite microtextures and record peak metamorphic conditions at 315 ± 40°C (XFe3+(chlorite) = 25-34%) and lower-temperature chlorite veins/microdomains at T = 210 ± 40°C (lower XFe3+(chlorite) = 40-45%). These results provide the first metamorphic constraints in textural context on the Barberton titanite microtextures and thereby improve our understanding of the local preservation conditions of these potential biosignatures. We suggest that this approach may prove to be an important tool in future studies to assess the biogenicity of these earliest candidate traces of life on Earth. Furthermore, we propose that this mapping approach could also be used to investigate altered mafic-ultramafic extraterrestrial samples containing candidate biosignatures.

Deciphering the dynamics of olivine nucleation and growth during antigorite breakdown

NASA Astrophysics Data System (ADS)

Dilissen, Nicole; Kahl, Wolf-Achim; Garrido, Carlos J.; López Sánchez-Vizcaíno, Vicente; Hidas, Károly

2016-04-01

Subduction zones are dynamic convergent plate boundaries associated with arc volcanism and earthquakes, which are believed to be controlled by fluids released during devolatilization reactions from the downgoing slab. The high-pressure breakdown of antigorite-serpentinite to prograde chlorite-harzburgite is considered to be the most significant source of water in subduction zones. The Cerro del Almirez ultramafic massif (Betic Cordillera, SE Spain) is a unique exhumed subduction terrane that preserves this dehydration reaction as a sharp front. A key to the understanding of the metamorphic conditions prevailing during serpentinite dehydration is to study the two prominent textures, granofels and spinifex-like chlorite harzburgite, which are the reaction products of antigorite breakdown. The textural study of these two types of Chl-harzburgite can provide insights into the kinetic of serpentinite dehydration reaction and the key factors controlling the overstepping of the reaction. Detailed mapping of textural variations in chlorite-harzburgite unveiled a network of granofels and spinifex-like lenses in the Almirez massif. In this work, we focus in the detailed textural variations across a well-exposed lens of spinifex-like chlorite-harzburgite, surrounded by granofels chlorite-harzburgite. This outcrop allowed us to make a very detailed oriented sampling (every 0.1-0.5 m across the 6 m thick lens) from the granofels into spinifex textures. The petrological study shows a developing transition of the olivine crystal shape, with premature mm-sized spinifex-like olivine crystals at the lens rims and well developed cm-sized spinifex-like grains in the core of the lens. The micro-CT study of oriented cores, together with EBSD study of thin sections from the same cores, allows the 3D reconstruction of olivine shapes and their lattice preferred orientation (LPO), constraining how olivine shapes and LPO differ from one texture to the other. This study provides valuable information on the kinetic of crystallization of olivine and how different textures formed in space and time, associated with the antigorite breakdown reaction.

Distinguishing Active Site Characteristics of Chlorite Dismutases with Their Cyanide Complexes.

PubMed

Geeraerts, Zachary; Celis, Arianna I; Mayfield, Jeffery A; Lorenz, Megan; Rodgers, Kenton R; DuBois, Jennifer L; Lukat-Rodgers, Gudrun S

2018-03-06

O 2 -evolving chlorite dismutases (Clds) efficiently convert chlorite (ClO 2 - ) to O 2 and Cl - . Dechloromonas aromatica Cld ( DaCld) is a highly active chlorite-decomposing homopentameric enzyme, typical of Clds found in perchlorate- and chlorate-respiring bacteria. The Gram-negative, human pathogen Klebsiella pneumoniae contains a homodimeric Cld ( KpCld) that also decomposes ClO 2 - , albeit with an activity 10-fold lower and a turnover number lower than those of DaCld. The interactions between the distal pocket and heme ligand of the DaCld and KpCld active sites have been probed via kinetic, thermodynamic, and spectroscopic behaviors of their cyanide complexes for insight into active site characteristics that are deterministic for chlorite decomposition. At 4.7 × 10 -9 M, the K D for the KpCld-CN - complex is 2 orders of magnitude smaller than that of DaCld-CN - and indicates an affinity for CN - that is greater than that of most heme proteins. The difference in CN - affinity between Kp- and DaClds is predominantly due to differences in k off . The kinetics of binding of cyanide to DaCld, DaCld(R183Q), and KpCld between pH 4 and 8.5 corroborate the importance of distal Arg183 and a p K a of ∼7 in stabilizing complexes of anionic ligands, including the substrate. The Fe-C stretching and FeCN bending modes of the DaCld-CN - (ν Fe-C , 441 cm -1 ; δ FeCN , 396 cm -1 ) and KpCld-CN - (ν Fe-C , 441 cm -1 ; δ FeCN , 356 cm -1 ) complexes reveal differences in their FeCN angle, which suggest different distal pocket interactions with their bound cyanide. Conformational differences in their catalytic sites are also reported by the single ferrous KpCld carbonyl complex, which is in contrast to the two conformers observed for DaCld-CO.

Mechanical Mixing and Metamorphism of Mafic and Ultramafic Lithologies during Mylonisis at the ST. Paul Transform System, Mid-Atlantic Ridge

NASA Astrophysics Data System (ADS)

Adrião, Á.; Maia, M.; Hemond, C.; Kaczmarek, M. A.; Briais, A.; Vincent, C.; Brunelli, D.

2017-12-01

The St. Paul Transform System offsets by 630 km the Equatorial Mid Atlantic Ridge at 1° N. It consists of four major faults separating three intra transform ridge axes. This region shows a transition from a transpressive, hot spot affected, regional-scale shear zone to the North to a region dominated by a particular oceanic core complex spreading to the South (Vincent et al., this congress). Samples collected in the region during the COLMEIA cruise (Maia et al., 2016) were studied for textures and whole-rock major and trace element contents. All samples experienced pervasive deformation at ductile to brittle conditions overprinted by late low-T alteration. Mylonitic and ultramylonitic rocks can be grouped in three main types: peridotitic, gabbroic and talc-chlorite schist. Peridotitic ultramylonites preserve few opx, cpx and sp porphyroclasts; they have homogeneous nano-micro grain size groundmass, banded foliation and late amphibole and sulfide crystallization. Locally S-C fabric overprints the mylonitic texture. Micro cracks, filled with serpentine, chlorite and oxides are common, as well fluid inclusions trails in olivine and plagioclase crystals of peridotite and gabbros respectively. Major and trace element content of the peridotitic mylonites plot in the depleted field of the abyssal peridotites; however, they present marked LREE enrichment and Eu positive anomaly. Gabbroic and talc-chlorite mylonites display REE-enriched patterns (up to 100x CI) and variable Eu anomalies. Major elements show a remarkable linear trend in the talc-chlorite group suggesting mixing of pure talc and chlorite end-members. These compositional characteristics suggest variable assimilation of MORB and E-MORB during mylonisis or early melt-rock interaction and hydrothermal evolution at variable metamorphic conditions. Vincent et al., 2017. Particular Oceanic Core Complex evolution …; this congress Maia et al., 2016. Extreme mantle uplift and exhumation ... Nat. Geo. doi:10.1038/ngeo2759

Evidence for low-grade metamorphism, hydrothermal alteration, and diagenesis on Mars from phyllosilicate mineral assemblages

USGS Publications Warehouse

Ehlmann, Bethany L.; Mustard, John F; Clark, Roger N.; Swayze, Gregg A.; Murchie, Scott L.

2011-01-01

The enhanced spatial and spectral resolution provided by the Compact Reconnaissance Imaging Spectrometer for Mars (CRISM) on the Mars Reconnaissance Orbiter (MRO) has led to the discovery of numerous hydrated silicate minerals on Mars, particularly in the ancient, cratered crust comprising the southern highlands. Phases recently identified using visible/near-infrared spectra include: smectite, chlorite, prehnite, high-charge phyllosilicates (illite or muscovite), the zeolite analcime, opaline silica, and serpentine. Some mineral assemblages represent the products of aqueous alteration at elevated temperatures. Geologic occurrences of these mineral assemblages are described using examples from west of the Isidis basin near the Nili Fossae and with reference to differences in implied temperature, fluid composition, and starting materials during alteration. The alteration minerals are not distributed homogeneously. Rather, certain craters host distinctive alteration assemblages: (1) prehnite-chlorite-silica, (2) analcime-silica-Fe,Mg-smectite-chlorite, (3) chlorite-illite (muscovite), and (4) serpentine, which furthermore has been found in bedrock units. These assemblages contrast with the prevalence of solely Fe,Mg-smectites in most phyllosilicate-bearing terrains on Mars, and they represent materials altered at depth then exposed by cratering. Of the minerals found to date, prehnite provides the clearest evidence for subsurface, hydrothermal/metamorphic alteration, as it forms only under highly restricted conditions (T = 200–400ºC). Multiple mechanisms exist for forming the other individual minerals; however, the most likely formation mechanisms for the characteristic mineralogic assemblages observed are, for (1) and (2), low-grade metamorphism or hydrothermal (<400ºC) circulation of fluids in basalt; for (3), transformation of trioctahedral smectites to chlorite and dioctahedral smectites to illite during diagenesis; and for (4), low-grade metamorphism or hydrothermal (<400ºC) circulation of fluids in ultramafic rocks. Evidence for high-grade metamorphism at elevated pressures or temperatures >400ºC has not been found.

Creep and Sliding in Clays Slopes: Mutual Effects of Interlayer Swelling and Ice Jacking.

DTIC Science & Technology

1984-01-11

chlorite 14% (6-21%) calcite 6,5% (1 - 15%) kaolinite 2% ( 1- 5%) dolomite 0,5% (0 - 4%) montmorillonite 23% (15-35%) Non clay phases 19% (15-30%) Clay...iconcretions, 200 mm coal lenses RE 3 4 Calcite N Quartz Feldspar Illite-muscovite Z Chlorite E Kaolinite montmori 1 loni te Fig. 10: Mineral content... montmorillonite , belong to a fluviatile fresh water cycle and are possibly influenced by volcanic ash falls. The series under investigation belongs to the upper

The fate of metaclinopyroxenite during serpentinite subduction

NASA Astrophysics Data System (ADS)

Padrón-Navarta, J. A.; Gómez-Pugnaire, M. T.; López Sánchez-Vizcaíno, V.; Garrido, C. J.; Marchesi, C.

2012-04-01

Subduction of the partially hydrated section of the lithosphere is widely accepted as the major water carrier to sub-arc depths. Geodynamic models and geochemical mass balances assume that this section is comprised almost exclusively by the maximum hydrated counterpart of harzburgite, i.e. antigorite-serpentinite. The common wisdom gained through the study of oceanic and continental lithospheric sequences indicates, however, that this assumption is an oversimplification and that the widespread occurrence of other lithologies, such as clinopyroxenites, should not be disregarded. It is obvious, however, that the role of these non-conventional lithologies in the subduction factory will also depend on their ability to record hydration and dehydration reactions. Here we report the textural and mineral assemblage evolution of clinopyroxene-tremolite bearing serpentinite, metaclinopyroxenite bodies and associated diopside-chlorite schists interlayered in serpentinites from the Cerro del Almirez (Betic Cordillera, Spain), the only place known where the high-pressure antigorite dehydration front is preserved (Trommsdorff et al., 1998; Padrón-Navarta et al., 2011). Cpx-Tr serpentinite bodies are unevenly distributed at the decametric scale in the serpentinite sequence and occurs as isoclinally foliated layers. Tremolite in these rocks was formed by the reaction: antigorite + diopside = tremolite + olivine + fluid [1] These rocks have been traditionally interpreted as strongly dismembered clinopyroxenite layers finely intermixed at the cm-scale with serpentinite. The following observations regarding the relationship between metaclinopyroxenite bodies and diopside-chlorite schists are, however, against this hypothesis. Detailed observations in almost undeformed coarse grained (cm-sized) metaclinopyroxenite bodies show that incipient transformation of mantle clinopyroxene occurs along former exsolution lamellae by the reaction: clinopyroxene + fluid = diopside + chlorite [2] Further deformation along these weak zones eventually results in the development of diopside-chlorite schists. The systematic lack of chlorite in Cpx-Tr serpentinite strongly suggests that these lithologies do not necessary represent an intermixing of antigorite-serpeninite with clinopyroxenite layers. Instead, they might be derived from more lherzolitic protoliths, where the Al-content in the mantle clinopyroxenes, and released during progressive metamorphism, was accommodated by antigorite (which can reach up to 3.5 wt. % Al2O3). Although rare, diopside-chlorite schists should then be considered as an important host for Ti and REE. Futhermore, the stability of this assemblage beyond the antigorite breakdown conditions has further implications for the deeper recycling of these elements in subduction zones. Padrón-Navarta, J.A., López Sánchez-Vizcaíno, V., Garrido, C.J., Gómez-Pugnaire, M.T., 2011. Metamorphic record of high-pressure dehydration of antigorite serpentinite to chlorite harzburgite in a subduction setting (Cerro del Almirez, Nevado-Filábride Complex, Southern Spain). J Petrology 52, 2047-2078. Trommsdorff, V., López Sánchez-Vizcaíno, V.L., Gómez-Pugnaire, M.T., Müntener, O, 1998. High pressure breakdown of antigorite to spinifex-textured olivine and orthopyroxene, SE Spain. Contrib Mineral Petr 132, 139-148.

Alteration minerals in impact-generated hydrothermal systems - Exploring host rock variability

NASA Astrophysics Data System (ADS)

Schwenzer, Susanne P.; Kring, David A.

2013-09-01

Impact-generated hydrothermal systems have been previously linked to the alteration of Mars’ crust and the production of secondary mineral assemblages seen from orbit. The sensitivity of the resultant assemblages has not yet been evaluated as a function of precursor primary rock compositions. In this work, we use thermochemical modeling to explore the variety of minerals that could be produced by altering several known lithologies based on martian meteorite compositions. For a basaltic host rock lithology (Dhofar 378, Humphrey) the main alteration phases are feldspar, zeolite, pyroxene, chlorite, clay (nontronite, kaolinite), and hematite; for a lherzolithic host rock lithology (LEW 88516) the main alteration phases are amphibole, serpentine, chlorite, clay (nontronite, kaolinite), and hematite; and for an ultramafic host rock lithology (Chassigny) the main minerals are secondary olivine, serpentine, magnetite, quartz, and hematite. These assemblages and proportions of phases in each of those cases depend on W/R and temperature. Integrating geologic, hydrologic and alteration mineral evidence, we have developed a model to illustrate the distribution of alteration assemblages that occur in different levels of an impact structure. At the surface, hot, hydrous alteration affects the ejecta and melt sheet producing clay and chlorite. Deeper in the subsurface and depending on the permeability of the rock, a variety of minerals - smectite, chlorite, serpentine, amphiboles and hematite - are produced in a circulating hydrothermal system. These modeled mineral distributions should assist with interpretation of orbital observations and help guide surface exploration by rovers and sample return assets.

Petrological evolution of subducted rodingite from seafloor metamorphism to dehydration of enclosing antigorite-serpentinite (Cerro del Almirez massif, southern Spain)

NASA Astrophysics Data System (ADS)

Laborda-López, Casto; López Sánchez-Vizcaíno, Vicente; Marchesi, Claudio; Gómez-Pugnaire, María Teresa; Garrido, Carlos J.; Jabaloy-Sánchez, Antonio; Padrón-Navarta, José Alberto

2016-04-01

Rodingites are common rocks associated with serpentinites in exhumed terrains that experienced subduction and high pressure metamorphism. However, the response of these rocks to devolatilization and redox reactions in subduction settings is not well constrained. In the Cerro del Almirez ultramafic massif (southern Spain) rodingites constitute about 1-2% of the total volume of exposed rocks. Metarodingites are enclosed in antigorite-serpentinite and chlorite-harzburgite separated by a transitional zone that represents the front of prograde serpentinite-dehydration in a paleo-subduction setting (Padrón-Navarta et al., 2011). Metarodingites occur as boudin lenses, 1 to 20 m in length and 30 cm to 2 m in thickness. During serpentinization of peridotite host rocks, dolerites and basalts precursor of rodingites underwent intense seafloor metasomatism, causing the enrichment in Ca and remobilization of Na and K. Subsequent metamorphism during subduction transformed the original igneous and seafloor metamorphic mineralogy into an assemblage of garnet (Ti-rich hydrogrossular), diopside, chlorite, and epidote. During prograde metamorphism, garnet composition changed towards higher andradite contents. High-pressure transformation of enclosing antigorite-serpentinite to chlorite-harzburgite released fluids which induced breakdown of garnet to epidote in metarodingites. Ti liberation by this latter reaction produced abundant titanite. Released fluids also triggered the formation of amphibole by alkalis addition. Highly recrystallized metarodingites in chlorite-harzburgite present a new generation of idiomorphic garnet with composition equal to 10-30% pyrope, 30-40% grossular and 35-55% almandine + spessartine. This garnet has titanite inclusions in the core and rutile inclusions in the rim. The contact between metarodingites and ultramafic rocks consists of a metasomatic zone (blackwall) with variable thickness (7 to 40 cm) constituted by chlorite, diopside, and titanite. Close to the contact with the blackwall, antigorite-serpentinite is very rich in diopside, olivine and Ti-clinohumite. In this study we present a thermodynamic model of phase relationships in rodingites and transitional blackwalls during their metamorphic history. We mainly aim to establish the evolution of P-T conditions experienced by metarodingites during subduction and the influence of fluids in the formation of mineral assemblages at different metamorphic stages. REFERENCES Padrón-Navarta, J.A., López Sánchez-Vizcaíno, V., Garrido, C.J., Gómez-Pugnaire, M.T., (2011): Metamorphic record of high-pressure dehydration of antigorite serpentinite to chlorite harzburgite in a subduction setting (Cerro Del Almirez, Nevado-Filábride Complex, Southern Spain). Journal of Petrology, 52, 2047-2078.

Chlorite, Biotite, Illite, Muscovite and Feldspar Dissolution Kinetics at Variable pH and Temperatures up to 280 deg C

DOE Data Explorer

Carroll, Susan; Smith, Megan M.; Lammers, Kristin

2017-02-24

Chemical reactions pose an important but poorly understood threat to EGS long-term success because of their impact on fracture permeability. This report summarizes the dissolution rate equations for layered silicates where data were lacking for geothermal systems. Here we report updated rate laws for chlorite (Carroll and Smith 2013), biotite (Carroll and Smith, 2015), illite (Carroll and Smith, 2014), and for muscovite. Also included is a spreadsheet with rate data and rate equations for use in reactive transport simulators.

Enhanced chlorine dioxide decay in the presence of metal oxides: relevance to drinking water distribution systems.

PubMed

Liu, Chao; von Gunten, Urs; Croué, Jean-Philippe

2013-08-06

Chlorine dioxide (ClO2) decay in the presence of typical metal oxides occurring in distribution systems was investigated. Metal oxides generally enhanced ClO2 decay in a second-order process via three pathways: (1) catalytic disproportionation with equimolar formation of chlorite and chlorate, (2) reaction to chlorite and oxygen, and (3) oxidation of a metal in a reduced form (e.g., cuprous oxide) to a higher oxidation state. Cupric oxide (CuO) and nickel oxide (NiO) showed significantly stronger abilities than goethite (α-FeOOH) to catalyze the ClO2 disproportionation (pathway 1), which predominated at higher initial ClO2 concentrations (56-81 μM). At lower initial ClO2 concentrations (13-31 μM), pathway 2 also contributed. The CuO-enhanced ClO2 decay is a base-assisted reaction with a third-order rate constant of 1.5 × 10(6) M(-2) s(-1) in the presence of 0.1 g L(-1) CuO at 21 ± 1 °C, which is 4-5 orders of magnitude higher than in the absence of CuO. The presence of natural organic matter (NOM) significantly enhanced the formation of chlorite and decreased the ClO2 disproportionation in the CuO-ClO2 system, probably because of a higher reactivity of CuO-activated ClO2 with NOM. Furthermore, a kinetic model was developed to simulate CuO-enhanced ClO2 decay at various pH values. Model simulations that agree well with the experimental data include a pre-equilibrium step with the rapid formation of a complex, namely, CuO-activated Cl2O4. The reaction of this complex with OH(-) is the rate-limiting and pH-dependent step for the overall reaction, producing chlorite and an intermediate that further forms chlorate and oxygen in parallel. These novel findings suggest that the possible ClO2 loss and the formation of chlorite/chlorate should be carefully considered in drinking water distribution systems containing copper pipes.

Understanding How the Distal Environment Directs Reactivity in Chlorite Dismutase: Spectroscopy and Reactivity of Arg183 Mutants

PubMed Central

Blanc, Béatrice; Mayfield, Jeffery A.; McDonald, Claudia A.; Lukat-Rodgers, Gudrun S.; Rodgers, Kenton R.; DuBois, Jennifer L.

2012-01-01

The chlorite dismutase from Dechloromonas aromatica (DaCld) catalyzes the highly efficient decomposition of chlorite to O2 and chloride. Spectroscopic, equilibrium thermodynamic, and kinetic measurements have indicated that Cld has two pH sensitive moieties; one is the heme, and Arg183 in the distal heme pocket has been hypothesized to be the second. This active site residue has been examined by site-directed mutagenesis to understand the roles of positive charge and hydrogen bonding in O–O bond formation. Three Cld mutants, Arg183 to Lys (R183K), Arg183 to Gln (R183Q), and Arg183 to Ala (R183A), were investigated to determine their respective contributions to the decomposition of chlorite ion, the spin state and coordination states of their ferric and ferrous forms, their cyanide and imidazole binding affinities, and their reduction potentials. UV–visible and resonance Raman spectroscopies showed that DaCld(R183A) contains five-coordinate high-spin (5cHS) heme, the DaCld(R183Q) heme is a mixture of five-coordinate and six-coordinate high spin (5c/6cHS) heme, and DaCld(R183K) contains six-coordinate low-spin (6cLS) heme. In contrast to wild-type (WT) Cld, which exhibits pKa values of 6.5 and 8.7, all three ferric mutants exhibited pH-independent spectroscopic signatures and kinetic behaviors. Steady state kinetic parameters of the chlorite decomposition reaction catalyzed by the mutants suggest that in WT DaCld the pKa of 6.5 corresponds to a change in the availability of positive charge from the guanidinium group of Arg183 to the heme site. This could be due to either direct acid–base chemistry at the Arg183 side chain or a flexible Arg183 side chain that can access various orientations. Current evidence is most consistent with a conformational adjustment of Arg183. A properly oriented Arg183 is critical for the stabilization of anions in the distal pocket and for efficient catalysis. PMID:22313119

Zeta Potential Measurements on Three Clays from Turkey and Effects of Clays on Coal Flotation

PubMed

Hussain; Dem&idot;rc&idot;; özbayoğlu

1996-12-25

There is a growing trend of characterizing coal and coal wastes in order to study the effect of clays present in them during coal washing. Coarse wastes from the Zonguldak Coal Washery, Turkey, were characterized and found to contain kaolinite, illite, and chlorite. These three clays, obtained in almost pure form from various locations in Turkey, have been subjected to X-ray diffraction (XRD) analysis to assess their purity and zeta potential measurements in order to evaluate their properties in terms of their surface charge and point of zero charge (pzc) values. It was found from XRD data that these clays were almost pure and their electrokinetic potential should therefore be representative of their colloidal behavior. All three clay minerals were negatively charged over the range from pH 2.5 to 11. Chlorite and illite have pzc at pH 3 and pH 2.5, respectively, whereas kaolinite has no pzc. The effect of these clays in Zonguldak coal, wastes, and black waters on coal flotation was studied by floating artificial mixtures of Zonguldak clean coal (4.5% ash) and individual clay. The flotation tests on coal/individual clay revealed that each clay influences coal flotation differently according to its type and amount. Illite had the worst effect on coal floated, followed by chlorite and kaolinite. The loss of yield in coal was found to be 18% for kaolinite, 20% for chlorite, and 28% for illite, indicating the worst effect of illite and least for kaolinite during coal flotation.

Provenance of Holocene sediment on the Chukchi-Alaskan margin based on combined diffuse spectral reflectance and quantitative X-Ray Diffraction analysis

USGS Publications Warehouse

Ortiz, J.D.; Polyak, L.; Grebmeier, J.M.; Darby, D.; Eberl, D.D.; Naidu, S.; Nof, D.

2009-01-01

Sediment clay and silt mineral assemblages provide an excellent means of assessing the provenance of fine-grained Arctic sediment especially when a unique mineral assemblage can be tied to specific source areas. The diffuse spectral reflectance (DSR) first derivative measurements and quantitative X-Ray Diffraction (qXRD) on a high-resolution sediment core from the continental slope north of Alaska constrain the sediment mineralogy. DSR results are augmented by measurements on several adjacent cores and compared to surface sediment samples from the northern Alaskan shelf and slope. Using Principal Component Analysis (PCA), we infer that the three leading DSR modes relate to mixtures of smectite + dolomite, illite + goethite, and chlorite + muscovite. This interpretation is consistent with the down core qXRD results. While the smectite + dolomite, and illite + goethite factors show increased variability down core, the chlorite + muscovite factor had highest positive loadings in the middle Holocene, between ca. 6.0 and 3.6??ka. Because the most likely source of the chlorite + muscovite suite in this vicinity lies in the North Pacific, we argue that the oscillations in chlorite + muscovite values likely reflect an increase in the inflow of Pacific water to the Arctic through the Bering Strait. The time interval of this event is associated in other parts of the globe with a non-linear response of the climate system to the decrease in insolation, which may be related to changes in water exchange between the Pacific and Arctic Ocean. ?? 2009 Elsevier B.V.

Peroxidase-type reactions suggest a heterolytic/nucleophilic O–O joining mechanism in the heme-dependent chlorite dismutase†

PubMed Central

Mayfield, Jeffrey A.; Blanc, Béatrice; Rodgers, Kenton R.; Lukat-Rodgers, Gudrun S.; DuBois, Jennifer L.

2015-01-01

Heme-containing chlorite dismutases (Clds) catalyze a highly unusual O–O bond forming reaction. The O–O cleaving reactions of hydrogen peroxide and peracetic acid (PAA) with the Cld from Dechloromonas aromatica (DaCld) were studied to better understand the Cl–O cleavage of the natural substrate and subsequent O–O bond formation. While reactions with H2O2 resulted in slow destruction of the heme, at acidic pH, heterolytic cleavage of the O–O bond of PAA cleanly yielded the ferryl porphyrin cation radical (Compound I). At alkaline pH, the reaction proceeds more rapidly and the first observed intermediate is a ferryl heme. Freezequench EPR confirmed that the latter has an uncoupled protein-based radical, indicating that Compound I is the first intermediate formed at all pH values and that radical migration is faster at alkaline pH. These results suggest by analogy that two-electron Cl–O bond cleavage to yield a ferryl-porphyrin cation radical is the most likely initial step in O–O bond formation from chlorite. PMID:24001266

Deposition of talc - kerolite-smectite - smectite at seafloor hydrothermal vent fields: Evidence from mineralogical, geochemical and oxygen isotope studies

USGS Publications Warehouse

Dekov, V.M.; Cuadros, J.; Shanks, Wayne C.; Koski, R.A.

2008-01-01

Talc, kerolite-smectite, smectite, chlorite-smectite and chlorite samples from sediments, chimneys and massive sulfides from six seafloor hydrothermal areas have been analyzed for mineralogy, chemistry and oxygen isotopes. Samples are from both peridotite- and basalt-hosted hydrothermal systems, and basaltic systems include sediment-free and sediment-covered sites. Mg-phyllosilicates at seafloor hydrothermal sites have previously been described as talc, stevensite or saponite. In contrast, new data show tri-octahedral Mg-phyllosilicates ranging from pure talc and Fe-rich talc, through kerolite-rich kerolite-smectite to smectite-rich kerolite-smectite and tri-octahedral smectite. The most common occurrence is mixed-layer kerolite-smectite, which shows an almost complete interstratification series with 5 to 85% smectitic layers. The smectite interstratified with kerolite is mostly tri-octahedral. The degree of crystal perfection of the clay sequence decreases generally from talc to kerolite-smectite with lower crystalline perfection as the proportion of smectite layers in kerolite-smectite increases. Our studies do not support any dependence of the precipitated minerals on the type/subtype of hydrothermal system. Oxygen isotope geothermometry demonstrates that talc and kerolite-smectite precipitated in chimneys, massive sulfide mounds, at the sediment surface and in open cracks in the sediment near seafloor are high-temperature (> 250????C) phases that are most probably the result of focused fluid discharge. The other end-member of this tri-octahedral Mg-phyllosilicate sequence, smectite, is a moderate-temperature (200-250????C) phase forming deep within the sediment (??? 0.8??m). Chlorite and chlorite-smectite, which constitute the alteration sediment matrix around the hydrothermal mounds, are lower-temperature (150-200????C) phases produced by diffuse fluid discharge through the sediment around the hydrothermal conduits. In addition to temperature, other two controls on the precipitation of this sequence are the silica activity and Mg/Al ratio (i.e. the degree of mixing of seawater with hydrothermal fluid). Higher silica activity favors the formation of talc relative to tri-octahedral smectite. Vent structures and sedimentary cover preclude complete mixing of hydrothermal fluid and ambient seawater, resulting in lower Mg/Al ratios in the interior parts of the chimneys and deeper in the sediment which leads to the precipitation of phyllosilicates with lower Mg contents. Talc and kerolite-smectite have very low trace- and rare earth element contents. Some exhibit a negative or flat Eu anomaly, which suggests Eu depletion in the original hydrothermal fluid. Such Eu depletion could be caused by precipitation of anhydrite or barite (sinks for Eu2+) deeper in the system. REE abundances and distribution patterns indicate that chlorite and chlorite-smectite are hydrothermal alteration products of the background turbiditic sediment. ?? 2007 Elsevier B.V. All rights reserved.

The Damage and Geochemical Signature of a Crustal Scale Strike-Slip Fault Zone

NASA Astrophysics Data System (ADS)

Gomila, R.; Mitchell, T. M.; Arancibia, G.; Jensen Siles, E.; Rempe, M.; Cembrano, J. M.; Faulkner, D. R.

2013-12-01

Fluid-flow migration in the upper crust is strongly controlled by fracture network permeability and connectivity within fault zones, which can lead to fluid-rock chemical interaction represented as mineral precipitation in mesh veins and/or mineralogical changes (alteration) of the host rock. While the dimensions of fault damage zones defined by fracture intensity is beginning to be better understood, how such dimensions compare to the size of alteration zones is less well known. Here, we show quantitative structural and chemical analyses as a function of distance from a crustal-scale strike-slip fault in the Atacama Fault System, Northern Chile, to compare fault damage zone characteristics with its geochemical signature. The Jorgillo Fault (JF) is a ca. 18 km long NNW striking strike-slip fault cutting Mesozoic rocks with sinistral displacement of ca. 4 km. In the study area, the JF cuts through orthogranulitic and gabbroic rocks at the west (JFW) and the east side (JFE), respectively. A 200 m fault perpendicular transect was mapped and sampled for structural and XRF analyses of the core, damage zone and protolith. The core zone consists of a ca. 1 m wide cataclasite zone bounded by two fault gouge zones ca. 40 cm. The damage zone width defined by fracture density is ca. 50 m wide each side of the core. The damage zone in JFW is characterized by NW-striking subvertical 2 cm wide cataclastic rocks and NE-striking milimetric open fractures. In JFE, 1-20 mm wide chlorite, quartz-epidote and quartz-calcite veins, cut the gabbro. Microfracture analysis in JFW reveal mm-wide cataclasitic/ultracataclasitic bands with clasts of protolith and chlorite orientated subparallel to the JF in the matrix, calcite veins in a T-fractures orientation, and minor polidirectional chlorite veins. In JFE, chlorite filled conjugate fractures with syntaxial growth textures and evidence for dilational fracturing processes are seen. Closest to the core, calcite veins crosscut chlorite veins. Whole-rock XRF analyses show Al and Ca content decrease with increasing Si, whereas Na increases towards the core. This can be interpreted as compositional changes of plagioclase to albite-rich ones due to chloritic-propylitic alteration. In the damage zone, LOI increases towards the core but decreases inside of it. This is explained by H2O-rich clays and gypsum in the fault core boundary represented as fault gouge zones whereas in the cataclastic core zone, the decrease in LOI is explained by epidote. Our results show the JF had an evolving permeability structure where a cataclasite-rich core is formed at an early stage, and then a gouge-bounded core is developed which acted as a barrier to fluid from east to west of the fault.

Mobility of gold during metamorphism of the Dalradian in Scotland

NASA Astrophysics Data System (ADS)

Pitcairn, I. K.; Skelton, A. D. L.; Wohlgemuth-Ueberwasser, C. C.

2015-09-01

Mobility of Au and related metals during metamorphism has been suggested to be the source of metals enriched in orogenic Au deposits. This study investigates the mobility of Au, As, and Sb during metamorphism of the Dalradian metasedimentary rocks of Scotland. The metamorphic processes in the Dalradian of Scotland are extremely well studied, and the terrane is an ideal area to investigate mobility of these metals. Our results show that of the 25 major and trace elements analysed, only Au, As, Sb, S and volatile contents as shown by loss on ignition (LOI) values show systematic variation with the metamorphic grade of the samples. Average Au concentrations decrease from 1.1 ± 0.55 ppb and 0.72 ± 0.34 ppb in chlorite and biotite zone rocks down to 0.4 ± 0.22 ppb and 0.34 ± 0.13 ppb in kyanite and sillimanite zone rocks. Average As concentrations decrease from 4.8 ppm (range 0.5 to 17.8 ppm) and 1.96 ± 1.9 ppm in chlorite and biotite zone rocks down to 0.24 ± 0.15 ppm and 0.2 ± 0.12 ppm in kyanite and sillimanite zone rocks. Average Sb concentrations decrease from 0.18 ± 0.15 ppm and 0.11 ± 0.10 ppm in chlorite and biotite zone rocks down to 0.04 ± 0.02 ppm in both kyanite and sillimanite zone rocks. Sulphur and LOI concentrations also show significant decreases. Mass balance calculations indicate that compared to chlorite and biotite zone samples, sillimanite zone samples have an average mass loss of 62 ± 14%, 94 ± 4% and 74 ± 14% for Au, As, and Sb respectively. Every 1 km3 of chlorite-biotite zone mixed psammitic-pelitic protolith rock that is metamorphosed to sillimanite zone conditions would release 1.5 t Au, 8613 t As, 270 t Sb, and 1.02 Mt S. The mobility of these elements is strongly controlled by the paragenesis of sulphide minerals. Pyrite, sphalerite, galena and cobaltite (as well as gersdorffite) decrease in abundance with increasing metamorphic grade in the Dalradian metasedimentary rocks. A critical aspect of the sulphide paragenesis is the transition of pyrite to pyrrhotite. This transition is complete by mid greenschist facies in the Loch Lomond samples but is more gradual at Glen Esk occurring between biotite and sillimanite zones. The Au, As, and Sb content of the sulphide assemblage also decreases with increasing metamorphic grade, and we suggest that this is a controlling factor on the mobility of these metals from the Dalradian metasedimentary rocks during metamorphism. Chlorite may be an important host mineral for As in the greenschist facies rocks. Breakdown of chlorite indirectly drives the mobility of Au, As, and Sb, as this produces the bulk of metamorphic fluid that drives transition between pyrite and pyrrhotite. We suggest that there is potential for significant undiscovered mineralisation in the Central and SW Highlands of Scotland. However, as the total mass of gold mobilised is lower than observed in other metasedimentary terranes such as the Otago and Alpine Schist's, New Zealand, very efficient fluid focussing and trapping mechanisms would be required to form large deposits in the Dalradian of Scotland.

Dimeric chlorite dismutase from the nitrogen‐fixing cyanobacterium C yanothece sp. PCC7425

PubMed Central

Schaffner, Irene; Hofbauer, Stefan; Krutzler, Michael; Pirker, Katharina F.; Bellei, Marzia; Stadlmayr, Gerhard; Mlynek, Georg; Djinovic‐Carugo, Kristina; Battistuzzi, Gianantonio; Furtmüller, Paul G.; Daims, Holger

2015-01-01

Summary It is demonstrated that cyanobacteria (both azotrophic and non‐azotrophic) contain heme b oxidoreductases that can convert chlorite to chloride and molecular oxygen (incorrectly denominated chlorite ‘dismutase’, Cld). Beside the water‐splitting manganese complex of photosystem II, this metalloenzyme is the second known enzyme that catalyses the formation of a covalent oxygen–oxygen bond. All cyanobacterial Clds have a truncated N‐terminus and are dimeric (i.e. clade 2) proteins. As model protein, Cld from C yanothece sp. PCC7425 (CCld) was recombinantly produced in E scherichia coli and shown to efficiently degrade chlorite with an activity optimum at pH 5.0 [k cat 1144 ± 23.8 s−1, KM 162 ± 10.0 μM, catalytic efficiency (7.1 ± 0.6) × 106 M−1 s−1]. The resting ferric high‐spin axially symmetric heme enzyme has a standard reduction potential of the Fe(III)/Fe(II) couple of −126 ± 1.9 mV at pH 7.0. Cyanide mediates the formation of a low‐spin complex with k on = (1.6 ± 0.1) × 105 M−1 s−1 and k off = 1.4 ± 2.9 s−1 (KD ∼ 8.6 μM). Both, thermal and chemical unfolding follows a non‐two‐state unfolding pathway with the first transition being related to the release of the prosthetic group. The obtained data are discussed with respect to known structure–function relationships of Clds. We ask for the physiological substrate and putative function of these O2‐producing proteins in (nitrogen‐fixing) cyanobacteria. PMID:25732258

Reaction softening by dissolution–precipitation creep in a retrograde greenschist facies ductile shear zone, New Hampshire, USA

USGS Publications Warehouse

McAleer, Ryan J.; Bish, David L.; Kunk, Michael J.; Sicard, Karri R.; Valley, Peter M.; Walsh, Gregory J.; Wathen, Bryan A.; Wintsch, R.P.

2016-01-01

We describe strain localization by a mixed process of reaction and microstructural softening in a lower greenschist facies ductile fault zone that transposes and replaces middle to upper amphibolite facies fabrics and mineral assemblages in the host schist of the Littleton Formation near Claremont, New Hampshire. Here, Na-poor muscovite and chlorite progressively replace first staurolite, then garnet, and finally biotite porphyroblasts as the core of the fault zone is approached. Across the transect, higher grade fabric-forming Na-rich muscovite is also progressively replaced by fabric-forming Na-poor muscovite. The mineralogy of the new phyllonitic fault-rock produced is dominated by Na-poor muscovite and chlorite together with late albite porphyroblasts. The replacement of the amphibolite facies porphyroblasts by muscovite and chlorite is pseudomorphic in some samples and shows that the chemical metastability of the porphyroblasts is sufficient to drive replacement. In contrast, element mapping shows that fabric-forming Na-rich muscovite is selectively replaced at high-strain microstructural sites, indicating that strain energy played an important role in activating the dissolution of the compositionally metastable muscovite. The replacement of strong, high-grade porphyroblasts by weaker Na-poor muscovite and chlorite constitutes reaction softening. The crystallization of parallel and contiguous mica in the retrograde foliation at the expense of the earlier and locally crenulated Na-rich muscovite-defined foliation destroys not only the metastable high-grade mineralogy, but also its stronger geometry. This process constitutes both reaction and microstructural softening. The deformation mechanism here was thus one of dissolution–precipitation creep, activated at considerably lower stresses than might be predicted in quartzofeldspathic rocks at the same lower greenschist facies conditions.

Efficacy of chlorine, acidic electrolyzed water and aqueous chlorine dioxide solutions to decontaminate Escherichia coli O157:H7 from lettuce leaves.

PubMed

Keskinen, Lindsey A; Burke, Angela; Annous, Bassam A

2009-06-30

This study compared the efficacy of chlorine (20-200 ppm), acidic electrolyzed water (50 ppm chlorine, pH 2.6), acidified sodium chlorite (20-200 ppm chlorite ion concentration, Sanova), and aqueous chlorine dioxide (20-200 ppm chlorite ion concentration, TriNova) washes in reducing populations of Escherichia coli O157:H7 on artificially inoculated lettuce. Fresh-cut leaves of Romaine or Iceberg lettuce were inoculated by immersion in water containing E. coli O157:H7 (8 log CFU/ml) for 5 min and dried in a salad spinner. Leaves (25 g) were then washed for 2 min, immediately or following 24 h of storage at 4 degrees C. The washing treatments containing chlorite ion concentrations of 100 and 200 ppm were the most effective against E. coli O157:H7 populations on Iceberg lettuce, with log reductions as high as 1.25 log CFU/g and 1.05 log CFU/g for TriNova and Sanova wash treatments, respectively. All other wash treatments resulted in population reductions of less than 1 log CFU/g. Chlorine (200 ppm), TriNova, Sanova, and acidic electrolyzed water were all equally effective against E. coli O157:H7 on Romaine, with log reductions of approximately 1 log CFU/g. The 20 ppm chlorine wash was as effective as the deionized water wash in reducing populations of E. coli O157:H7 on Romaine and Iceberg lettuce. Scanning electron microscopy indicated that E. coli O157:H7 that was incorporated into biofilms or located in damage lettuce tissue remained on the lettuce leaf, while individual cells on undamaged leaf surfaces were more likely to be washed away.

Chlorite, Biotite, Illite, Muscovite, and Feldspar Dissolution Kinetics at Variable pH and Temperatures up to 280 C

DOE Office of Scientific and Technical Information (OSTI.GOV)

Carroll, S.; Smith, M.; Lammers, K.

2016-10-05

Summary Sheet silicates and clays are ubiquitous in geothermal environments. Their dissolution is of interest because this process contributes to scaling reactions along fluid pathways and alteration of fracture surfaces, which could affect reservoir permeability. In order to better predict the geochemical impacts on long-term performance of engineered geothermal systems, we have measured chlorite, biotite, illite, and muscovite dissolution and developed generalized kinetic rate laws that are applicable over an expanded range of solution pH and temperature for each mineral. This report summarizes the rate equations for layered silicates where data were lacking for geothermal systems.

Characterizing Isozymes of Chlorite Dismutase for Water Treatment

PubMed Central

Mobilia, Kellen C.; Hutchison, Justin M.; Zilles, Julie L.

2017-01-01

This work investigated the potential for biocatalytic degradation of micropollutants, focusing on chlorine oxyanions as model contaminants, by mining biology to identify promising biocatalysts. Existing isozymes of chlorite dismutase (Cld) were characterized with respect to parameters relevant to this high volume, low-value product application: kinetic parameters, resistance to catalytic inactivation, and stability. Maximum reaction velocities (Vmax) were typically on the order of 104 μmol min-1 (μmol heme)-1. Substrate affinity (Km) values were on the order of 100 μM, except for the Cld from Candidatus Nitrospira defluvii (NdCld), which showed a significantly lower affinity for chlorite. NdCld also had the highest susceptibility to catalytic inactivation. In contrast, the Cld from Ideonella dechloratans was least susceptible to catalytic inactivation, with a maximum turnover number of approximately 150,000, more than sevenfold higher than other tested isozymes. Under non-reactive conditions, Cld was quite stable, retaining over 50% of activity after 30 days, and most samples retained activity even after 90–100 days. Overall, Cld from I. dechloratans was the most promising candidate for environmental applications, having high affinity and activity, a relatively low propensity for catalytic inactivation, and excellent stability. PMID:29312158

Chlorine dioxide-induced and Congo red-inhibited Marangoni effect on the chlorite-trithionate reaction front

NASA Astrophysics Data System (ADS)

Liu, Yang; Ren, Xingfeng; Pan, Changwei; Zheng, Ting; Yuan, Ling; Zheng, Juhua; Gao, Qingyu

2017-10-01

Hydrodynamic flows can exert multiple effects on an exothermal autocatalytic reaction, such as buoyancy and the Marangoni convection, which can change the structure and velocity of chemical waves. Here we report that in the chlorite-trithionate reaction, the production and consumption of chlorine dioxide can induce and inhibit Marangoni flow, respectively, leading to different chemo-hydrodynamic patterns. The horizontal propagation of a reaction-diffusion-convection front was investigated with the upper surface open to the air. The Marangoni convection, induced by gaseous chlorine dioxide on the surface, produced from chlorite disproportionation after the proton autocatalysis, has the same effect as the heat convection. When the Marangoni effect is removed by the reaction of chlorine dioxide with the Congo red (CR) indicator, an oscillatory propagation of the front tip is observed under suitable conditions. Replacing CR with bromophenol blue (BPB) distinctly enhanced the floating, resulting in multiple vortexes, owing to the coexistence between BPB and chlorine dioxide. Using the incompressible Navier-Stokes equations coupled with reaction-diffusion and heat conduction equations, we numerically obtain various experimental scenarios of front instability for the exothermic autocatalytic reaction coupled with buoyancy-driven convection and Marangoni convection.

Blueschist metamorphism and its tectonic implication of Late Paleozoic-Early Mesozoic metabasites in the mélange zones, central Inner Mongolia, China

NASA Astrophysics Data System (ADS)

Zhang, Jinrui; Wei, Chunjing; Chu, Hang

2015-01-01

Blueschists in central Inner Mongolia are distributed as layers and blocks in mélanges including the southern zone in Ondor Sum area and the northern zone in Manghete and Naomuhunni areas. They have been attributed to the subduction of Early Paleozoic oceanic crust. Blueschists from Ondor Sum and Naomuhunni are characterized by occurrence of sodic amphibole coexisting with epidote, albite, chlorite, calcic amphibole (in Ondor Sum) and muscovite (in Naomuhunni). Blueschists in Manghete contain porphyroblastic albite with inclusions of garnet and epidote in a matrix dominated by calcic-sodic amphibole, epidote, chlorite, albite and muscovite. Phase equilibria modeling for three blueschist samples using pseudosection suggest that the AlM2 contents in sodic amphibole can be used as a good barometer in the limited assemblage involving sodic amphibole + actinolite + epidote + chlorite + albite + quartz under pressures <4-6 kbar, while this barometer is largely influenced by temperature and bulk Fe2O3 contents in the actinolite-absent assemblage sodic amphibole + epidote + chlorite + albite + quartz of higher pressure and the AlM2 contents are not pressure-controlled in the albite-absent assemblage sodic amphibole + epidote + chlorite + quartz under pressures > 7-10 kbar. In the sodic amphibole-bearing assemblages, the NaM4 contents in sodic amphibole mainly decrease as temperature rises, being a potential thermometry. The calculated pseudosections constrain the P-T conditions of blueschists to be 3.2-4.2 kbar/355-415 °C in Ondor Sum, 8.2-9.0 kbar/455 °C-495 °C in Manghete and 6.6-8.1 kbar/420-470 °C in Naomuhunni. These P-T estimates indicate a rather high geothermal gradient of 18-25 °C/km for the blueschist metamorphism, being of intermediate P/T facies series. Available zircon U-Pb age data suggests that the protoliths of blueschists were formed later than Late Paleozoic-Early Mesozoic and metamorphosed soon afterwards. An alternative interpretation for the tectonic implication of blueschists in central Inner Mongolia is that they may be a new type attributed to closure of limited ocean basins and do not represent a tectonic regime occurred in conventional subduction setting.

Chemistry, mineralogy and alteration intensity of hydrothermal altered Mt Unzen conduit rocks (Shimabara/Japan)

NASA Astrophysics Data System (ADS)

Hess, Kai-Uwe; Yilmaz, Tim; Gilg, H. Albert; Janots, Emilie; Mayer, Klaus; Nakada, Setsuya; Dingwell, Donald

2017-04-01

Investigations were carried out on hydrothermally altered coherent dacitic dykes samples from (USDP-4) drill core at Mt Unzen stratovolcano (Shimabara/Japan). XRF, XRD, EMPA, C-O-isotope, hot-cathode CL and SEM analysis led to insights concerning chemistry, mineralogy, and intensity and type of alteration as well as the origin of carbonate-precipitating fluids. Additionally a textural characterization of the occurring replacement features in the volcanic conduit rocks was performed. The occurrence of the main secondary phases such as chlorite, pyrite, carbonates, and R1 (Reichweite parameter) illite-smectite and kaolinite group minerals indicate a weak to moderate propylitic to phyllic hydrothermal alteration. The dacitic samples of the dykes show different hydrothermal alteration features: (i) carbonate and chlorite pseudomorphs after hornblende as well as core and zonal textures due to replacement of plagioclase by R1 illite-smectite as well as kaolinite group minerals, (ii) colloform banded fracture fillings and fillings in dissolution vugs, and (iii) chlorite, R1 illite-smectite as well as kaolinite group minerals in the groundmass. Late chlorite veins crosscut precipitates of R1 illite-smectite as well as kaolinite group minerals. Carbonates in fractures and in pseudomorphs after hornblende comprise iron-rich dolomite solid solutions ("ankerite") and calcite. Isotopic values indicate a hydrothermal-magmatic origin for the carbonate formation. The chlorite-carbonate-pyrite index (CCPI) and the Ishikawa alteration index (AI), applied to the investigated samples show significant differences (CCPI=52.7-57.8; AI=36.1-40.6) indicating their different degree of alteration. According to Nakada et al., 2005, the C13 to C16 dykes represent the feeder dyke from the latest eruption (1991-1995) whereas C8 represents an earlier dyke feeder dyke from an older eruption. Weakest alteration, which was obtained in samples C16-1-5 and C13-2-5, correlates with the alteration degree of the pristine dome rocks. The highest CCPI value was determined for sample C14-1-5 and the highest AI value was determined for sample C15-2-6. The degrees of alteration do not indicate highest alteration of the samples C8-1-2 and C8-2-1 from the older dykes.

Environment of ore deposition in the Creede mining district, San Juan Mountains, Colorado; Part IV, source of fluids, from oxygen, hydrogen, and carbon isotope studies

USGS Publications Warehouse

Bethke, P.M.; Rye, R.O.

1979-01-01

The hydrogen isotopic composition of fluids responsible for formation of the near-surface silver-base metal vein deposits at Creede was measured by direct analysis of inclusion fluids in sphalerite, quartz, and rhodochrosite and was estimated from analyses of illite and chlorite. The oxygen isotopic composition was determined directly on inclusion fluids in sphalerite and was estimated from analyses of quartz, illite, rhodochrosite, siderite, and adularia. The carbon isotopic composition was estimated from analyses of rhodochrosite and siderite. The ranges in isotopic composition for water and CO2 in the fluids associated with the formation of each of the minerals is given below (number of determinations given in parentheses):Mineral delta D (sub H2) O ppm delta 18 O (sub H2) O ppm delta 13 C (sub CO2) ppmSphalerite -81 to -54 (4) -10.1 to -4.5 (4)Quartz -97 to -86 (4) -5.9 to 1.8 (18)Illite -62 to -50 (8) -1.6 to 1.2(7)Chlorite -64 to -55 (10) -2.2 to 0.8 (10)Adularia 4.2 (1)Rhodochrosite -82 to -78 (2) 4.2 to 9.4 (9) -5.7 to -4.2 (9)Siderite 4.9 to 9.9 (6) -6.9 to -2.7 (6)The delta D (sub H2) O and delta 18 O (sub H2) O values of fluids associated with the formation of sphalerite, quartz, illite/chlorite, and carbonate minerals differ substantially from one another, and these differences appear to have been maintained throughout the depositional history, regardless of the positions of the minerals in the paragenetic sequence.The data suggest that waters from three coexisting reservoirs fed the vein system alternately and episodically during vein formation, and apparently there was little mixing of the fluids from the different reservoirs. The hydrogen, oxygen, and carbon isotope data suggest that the carbonate waters were deep seated, probably dominantly magmatic, in origin. The sphalerite and illite/chlorite waters must have been dominantly meteoric in origin and substantially oxygen shifted by exchange with the volcanic country rocks. The quartz waters were also oxygen shifted meteoric waters but were some 40 per mil lower in deuterium content than the sphalerite and illite/chlorite waters.We propose that the quartz fluids entered the vein system from reservoirs beneath the mountainous areas to the north in the vicinity of the present Continental Divide, but that the sphalerite and illite/chlorite fluids entered the vein system from a topographically low area to the south along the structural moat of the Creede caldera. The difference in delta D between the two meteoric waters may reflect differences in altitude of the recharge areas for the two reservoirs or may be clue to isotopic evolution of the closed-basin lake and interstitial waters in the moat surrounding the Creede caldera.

Oxygen-isotope, X-ray-diffraction and scanning-electron-microscope examinations of authigenic-layer-silicate minerals from Mississippian and Pennsylvanian sandstones in the Michigan Basin

USGS Publications Warehouse

Zacharias, K.F.; Sibley, D.F.; Westjohn, D.B.; Weaver, T. L.

1993-01-01

Oxygen-isotope compositions of authigenic-layer silicates (<2-micrometer fraction) extracted from Mississippian and Pennsylvanian sandstones in the Lower Peninsula of Michigan were determined. Petrographic and scanning-electron-microscope examinations, and X-ray diffractograms show that chlorite and kaolinite are the most common authigenic-layer silicates in Mississippian sandstones. The range of oxygen-isotope compositions of chlorite and kaolinite are +10.3 to +11.9 and +12.9 to +19.3 pars per thousand (per mil) (relative to Standard Mean Ocean Water), respectively. Kaolinite is the only authigenic-isotopic compositions of kaolinite range from +16.8 to +19.0 per mil.

Comparative study of microfacies variation in two samples from the Chittenango member, Marcellus shale subgroup, western New York state, USA

DOE Office of Scientific and Technical Information (OSTI.GOV)

Balulla, Shama, E-mail: shamamohammed77@outlook.com; Padmanabhan, E., E-mail: eswaran-padmanabhan@petronas.com.my; Over, Jeffrey, E-mail: over@geneseo.edu

This study demonstrates the significant lithologic variations that occur within the two shale samples from the Chittenango member of the Marcellus shale formation from western New York State in terms of mineralogical composition, type of lamination, pyrite occurrences and fossil content using thin section detailed description and field emission Scanning electron microscope (FESEM) with energy dispersive X-Ray Spectrum (EDX). This study is classified samples as laminated clayshale and fossiliferous carbonaceous shale. The most important detrital constituents of these shales are the clay mineral illite and chlorite, quartz, organic matter, carbonate mineral, and pyrite. The laminated clayshale has a lower amountmore » of quartz and carbonate minerals than fossiliferous carbonaceous shale while it has a higher amount of clay minerals (chlorite and illite) and organic matter. FESEM analysis confirms the presence of chlorite and illite. The fossil content in the laminated clayshale is much lower than the fossiliferous carbonaceous shale. This can provide greater insights about variations in the depositional and environmental factors that influenced its deposition. This result can be compiled with the sufficient data to be helpful for designing the horizontal wells and placement of hydraulic fracturing in shale gas exploration and production.« less

Evaluation of Sanitizing Methods for Reducing Microbial Contamination on Fresh Strawberry, Cherry Tomato, and Red Bayberry.

PubMed

Wei, Wei; Wang, Xu; Xie, Zhongwen; Wang, Wen; Xu, Junfeng; Liu, Yuanjing; Gao, Haiyan; Zhou, Yu

2017-01-01

Strawberries, cherry tomatoes, and red bayberries, which are the most popular types of fresh produce in China, are vulnerable to microbial contamination. In this study, different sanitizing methods [treatment with 2% organic acids, 0.02% sodium hypochlorite (SH), 0.1% sodium chlorite (SC), and 0.1% acidified sodium chlorite (ASC)] were applied to fresh strawberry, cherry tomato, and red bayberry, and their abilities to reduce aerobic bacteria, Escherichia coli O157:H7, mold, yeast, and Salmonella Typhimurium were evaluated. The commercially used SH method reduced the background microbiota on strawberry, cherry tomato, and red bayberry by 0.20-2.07 log cfu/g. The ASC method reduced background microbiota (except for mold) on strawberry and cherry tomato by more than 3.0 log cfu/g. ASC was the only sanitizer that significantly reduced mold on red bayberry, and lactic acid was the only organic acid sanitizer that effectively reduced yeast on red bayberry. The ASC method had the best sterilizing effect on the three fresh fruits and also required the shortest sanitizing time and low chlorite content. The application of ASC method significantly reduced the microbiota on retail grocery samples, and the effect was similar to that achieved by sanitizing methods comparison.

Evaluation of Sanitizing Methods for Reducing Microbial Contamination on Fresh Strawberry, Cherry Tomato, and Red Bayberry

PubMed Central

Wei, Wei; Wang, Xu; Xie, Zhongwen; Wang, Wen; Xu, Junfeng; Liu, Yuanjing; Gao, Haiyan; Zhou, Yu

2017-01-01

Strawberries, cherry tomatoes, and red bayberries, which are the most popular types of fresh produce in China, are vulnerable to microbial contamination. In this study, different sanitizing methods [treatment with 2% organic acids, 0.02% sodium hypochlorite (SH), 0.1% sodium chlorite (SC), and 0.1% acidified sodium chlorite (ASC)] were applied to fresh strawberry, cherry tomato, and red bayberry, and their abilities to reduce aerobic bacteria, Escherichia coli O157:H7, mold, yeast, and Salmonella Typhimurium were evaluated. The commercially used SH method reduced the background microbiota on strawberry, cherry tomato, and red bayberry by 0.20–2.07 log cfu/g. The ASC method reduced background microbiota (except for mold) on strawberry and cherry tomato by more than 3.0 log cfu/g. ASC was the only sanitizer that significantly reduced mold on red bayberry, and lactic acid was the only organic acid sanitizer that effectively reduced yeast on red bayberry. The ASC method had the best sterilizing effect on the three fresh fruits and also required the shortest sanitizing time and low chlorite content. The application of ASC method significantly reduced the microbiota on retail grocery samples, and the effect was similar to that achieved by sanitizing methods comparison. PMID:29259594

Disinfection aboard cruise liners and naval units: formation of disinfection by-products using chlorine dioxide in different qualities of drinking water.

PubMed

Ufermann, Petra; Petersen, Hauke; Exner, Martin

2011-12-01

The world-wide deployment of cruise liners and naval units has caused an increased need for the disinfection of drinking water. The main cause for this is the unknown quality of drinking water in foreign harbours--besides the formation of bio-films due to the climatically disadvantageous conditions in the operational area. Water conduits on board are currently disinfected with calcium hypochlorite in case of microbiological contamination. Chemical and physical analyses after disinfection with calcium hypochlorite have shown that organic by-products consisting of trihalomethanes develop in considerable amounts during disinfection. Furthermore, the method is susceptible to handling errors and thus often leads to insufficient disinfection results. Hitherto, the use of other disinfection methods allowed by government regulations, especially chlorine dioxide, is not widely spread. Unlike disinfection with calcium hypochlorite, chlorine dioxide does not lead to the formation of trihalomethanes. Typical disinfection by-products (DBP) are the anions chlorite and chlorate, which are formed in oxidative processes. The formation conditions of these anions have not yet been elucidated. For this reason, the probability of the generation of inorganic by-products after disinfection with chlorine dioxide has been determined, and their occurrence in drinking water on board has been examined with respect to a possible correlation between water quality and the formation of chlorate and chlorite. Therefore, a chromatographic method was developed and validated in order to determine the periodical development of chlorate and chlorite from chorine dioxide in purified water at different pH-values as well as in actual drinking water samples from water conduits on board. The formation of the by-products chlorite and chlorate after disinfection with chlorine dioxide is influenced neither by pH-value nor by chemical properties of the disinfected water. Considering the examined conditions, chlorine dioxide is suitable for usage on board due to its simple handling and the low potential of producing by-products. Copyright © 2011 Elsevier GmbH. All rights reserved.

Abiotic CO2 reduction during geologic carbon sequestration facilitated by Fe(II)-bearing minerals

NASA Astrophysics Data System (ADS)

Nielsen, L. C.; Maher, K.; Bird, D. K.; Brown, G. E.; Thomas, B.; Johnson, N. C.; Rosenbauer, R. J.

2012-12-01

Redox reactions involving subsurface minerals and fluids and can lead to the abiotic generation of hydrocarbons from CO2 under certain conditions. Depleted oil reservoirs and saline aquifers targeted for geologic carbon sequestration (GCS) can contain significant quantities of minerals such as ferrous chlorite, which could facilitate the abiotic reduction of carbon dioxide to n-carboxylic acids, hydrocarbons, and amorphous carbon (C0). If such reactions occur, the injection of supercritical CO2 (scCO2) could significantly alter the oxidation state of the reservoir and cause extensive reorganization of the stable mineral assemblage via dissolution and reprecipitation reactions. Naturally occurring iron oxide minerals such as magnetite are known to catalyze CO2 reduction, resulting in the synthesis of organic compounds. Magnetite is thermodynamically stable in Fe(II) chlorite-bearing mineral assemblages typical of some reservoir formations. Thermodynamic calculations demonstrate that GCS reservoirs buffered by the chlorite-kaolinite-carbonate(siderite/magnesite)-quartz assemblage favor the reduction of CO2 to n-carboxylic acids, hydrocarbons, and C0, although the extent of abiotic CO2 reduction may be kinetically limited. To investigate the rates of abiotic CO2 reduction in the presence of magnetite, we performed batch abiotic CO2 reduction experiments using a Dickson-type rocking hydrothermal apparatus at temperatures (373 K) and pressures (100 bar) within the range of conditions relevant to GCS. Blank experiments containing CO2 and H2 were used to rule out the possibility of catalytic activity of the experimental apparatus. Reaction of brine-suspended magnetite nanoparticles with scCO2 at H2 partial pressures typical of reservoir rocks - up to 100 and 0.1 bars respectively - was used to investigate the kinetics of magnetite-catalyzed abiotic CO2 reduction. Later experiments introducing ferrous chlorite (ripidolite) were carried out to determine the potential for heterogeneous catalysis in GCS systems.

Specific Features of Profile Distribution and Crystallochemistry of Phyllosilicates in Soils of the Cisbaikal Forest-Steppe

NASA Astrophysics Data System (ADS)

Chizhikova, N. P.; Gamzikov, G. P.; Chechetko, E. S.

2018-01-01

The mineralogical composition of agrogray, dark gray, and agro-dark gray soils (Luvic Greyzemic Retic Phaeozems); agro-dark gray residual-calcareous soils (Calcaric Cambic Phaeozems); clay-illuvial agrochernozems (Luvic Chernic Phaeozems); and agrochernozems with migrational-mycelial carbonates (Haplic Chernozems) developed in the forest-steppe of Central Siberia within the Irkutsk Depression has been studied. The clay (<1 μm) fraction separated from these soils consists of mixed-layer minerals with alternating layers of hydromica, smectite, vermiculite, and chlorite; the proportions between them change within the soil profiles. The clay fraction also contains hydromicas, kaolinite, chlorite, and some admixture of the fine-dispersed quartz. Each type of the soils is characterized by its own distribution pattern of clay material with specific alternation of layers in the mixed-layer formations. Mixed-layer minerals of the chlorite-vermiculite type predominate in the upper horizons of texture-differentiated soils. Down the soil profile, the content of mixed-layer mica-smectitic minerals increases. In the clay fraction of arable dark gray-humus soils with residual carbonates, the distribution of the clay fraction and major mineral phases in the soil profile is relatively even. An increased content of well-crystallized kaolinite is typical of these soils. The parent material of agrochernozems has a layered character: the upper horizons are generally depleted of clay, and the middle-profile and lower horizons are characterized by the considerable kaolinite content. In general, the clay material of soils of the Tulun-Irkutsk forest-steppe differs considerably from the clay material of foreststeppe soils developed from loesslike and mantle loams in the European part of Russia. In particular, this difference is seen in the proportions between major mineral phases and between biotitic and muscovitic components, as well as in the degree of crystallinity and behavior of kaolinite and chlorite.

Diagenesis and reservoir quality of Bhuban sandstones (Neogene), Titas Gas Field, Bengal Basin, Bangladesh

NASA Astrophysics Data System (ADS)

Aminul Islam, M.

2009-06-01

This study deals with the diagenesis and reservoir quality of sandstones of the Bhuban Formation located at the Titas Gas Field of Bengal Basin. Petrographic study including XRD, CL, SEM and BSE image analysis and quantitative determination of reservoir properties were carried out for this study. The sandstones are fine to medium-grained, moderately well to well sorted subfeldspathic arenites with subordinate feldspathic and lithic arenites. The diagenetic processes include clay infiltration, compaction and cementation (quartz overgrowth, chlorite, kaolinite, calcite and minor amount of pyrite, dolomite and K-feldspar overgrowth). Quartz is the dominant pore occluding cement and generally occurred as small euhedral crystals, locally as large pyramidal crystals in the primary pores. Pressure solution derived from grain contact is the main contributor of quartz overgrowths. Chlorite occurs as pore-lining and pore filling cement. In some cases, chlorite helps to retain porosity by preventing quartz overgrowth. In some restricted depth interval, pore-occlusion by calcite cement is very much intense. Kaolinite locally developed as vermiform and accelerated the minor porosity loss due to pore-occlusion. Kaolinite/chlorite enhances ineffective microporosity. Kaolinite is a by-product of feldspar leaching in the presence of acidic fluid produced during the maturation of organic matter in the adjacent Miocene or deeper Oligocene source rocks. The relation between diagenesis and reservoir quality is as follows: the initial porosity was decreased by compaction and cementation and then increased by leaching of the metastable grains and dissolution of cement. Good quality reservoir rocks were deposited in fluvial environment and hence quality of reservoir rocks is also environment selective. Porosity and permeability data exhibit good inverse correlation with cement. However, some data points indicate multiple controls on permeability. Reservoir quality is thus controlled by pore occluding cement, textural parameters (grain size, pore size and sorting) and depositional environment. The reservoir finally resumed partly its pre-cementation quality after development of secondary porosity.

The Geology and Petrography of Yücebelen and Surrounding Area, Torul-Gümüşhane

NASA Astrophysics Data System (ADS)

Doǧacan, Özcan; Özpınar, Yahya

2013-04-01

The study area is located in the tectono-stratigraphic zone named "Eastern Pontide Zone" from the northeastern part of Turkey. Eastern Pontides were formed by the subduction of Tethys Ocean under the Eurasian plate, during the Early Cretaceous - Late Eocene. Eastern Pontide orogenic zone can be divided in two tectono-stratigraphic subgroups as the northern and southern zones. The study area is located very close to border of these two subgroups but located in northern zone. In this project, the first geological map of the study area at the scale 1:5000 was made. Subsequently, detailed geological maps at the scale 1:2000 were made for the areas rich in ores. In the study area, Upper Cretaceous volcanic rocks consisting of basalts and basaltic andesites take place at the bottom of the rock sequence. Basalts and basaltic andesites with hyaloophitic, vitrophiric and microporphyric texture comprise plagioclase +pyroxene +chlorite +calcite ±epidote ±chalcedony ±opaque minerals. They are overlain by concordant pyroclastic and dacitic-rhyodacitic rocks. Quarts + K-feldispar ±plagioclase? ±biotite ±chlorite ±calcite ±chalcedony minerals are determined as a result of microscope investigation on samples taken from these rocks. These rocks are overlain by sedimentary rocks intercalated with pyroclastic rocks. All those units mentioned above, were intruded by granitoids of supposed Upper Cretaceous-Eocene age. Granitoids that crop out in the area were classified in terms of Q-ANOR parameters as granodiorites (Adile Hamlet occurrence - investigated in detail), diorites (Tuzlak Hill occurrence- eastern-part of study area) and quartz monzodiorites (İstavroma Hill occurrence- northern part of study area). Adile Hamlet granodiorites comprise plagioclase +pyroxene +chlorite +calcite ±quarts ±epidote +opaque minerals. A sequence of quarts +orthoclase +plagioclase ±chlorite ±epidote ±calcite ±opaque minerals have been determined after investigation of the rock samples collected from Tuzlak Hill surrounding area. Also, petrographic investigation gave us plagioclase +hornblende ±biotite ±chlorite ±calcite ±quarts ±opaque minerals mineral sequence for the occurrences seen around İstavroma Hill. All of these units are intruded Late Eocene andesitic and dacitic dykes. It was determined that Cu-Pb-Zn mineralization depends on the quartz veins developed in the fracture zones of the granitoid body and its contacts with sedimentary rocks. These veins revealed a paragenesis consisting Cu-Pb-Zn minerals. Key words: Eastern Pontides, Gümüşhane-Torul, Granitoid, Cu-Pb-Zn mineralization, Gümüşhane-Torul

Steatite and schist as contenders for the Global Heritage Stone Resource due to their importance in Brazil's natural stone built heritage

NASA Astrophysics Data System (ADS)

Gilberto Costa, Antônio

2013-04-01

In Brazil, European natural stones, such as marble and limestone, were used as building material at historically important buildings and monuments, mainly in coastal cities, as well as in contemporary urban centers. However, in the country's central region, these Italian and Portuguese marbles and limestones were scarcely used. Instead, they were substituted for soapstone and several types of schist. As of 1755, the former was employed because of the ease with which it can be worked, essentially in the sculptural art and in the production of ornamental elements. Characterized by the presence of talc, steatite can feature other minerals such as serpentine, chlorite, carbonate, amphiboles, oxides like hematite and magnetite, and sulfites like pyrite, all in broadly variable amounts, which can result in modification of its technological properties (Volumetric Weight, Porosity, Water Absorption, Uniaxial Compression, Abrasion Resistance, Thermal Expansion etc.). In such rocks, talc content will be a decisive factor in their coloration. The higher its talc content is the clearer and softer the stone type will be, which ends up being known as talc stone. In such cases, the rock can display different hues of green, blue and gray. When compared to other rocks, texture patterns containing talc crystals, chlorite and carbonate contribute to low absorption and porosity for steatites. Schists were equally used at historical buildings in the Brazilian inland, especially in constructions in Minas Gerais towns, both in the production of structural elements such as bases, corners, pillars and foundations and in the creation of ornaments. Featuring different compositions, such rocks - which almost always occur interlayered with other ones such as quartzite - display coloration ranging from hues of gray to green to blue. They can be quartz-sericite-albite-chlorite schists featuring great or no amounts of carbonate, magnetite, epidote and tourmaline, sometimes with garnet, such as in some of Caeté's monuments. They can range from silverfish to light green, such as the quartz-sericite schist from Diamantina, some of which contain variable amounts of kyanite, chlorite, or even chloritoid, as well as the presence of whitish bands rich with carbonate and quartz crystals, such as in Caeté and Sabará. They can be serpentine schist and chlorite schist, from quarries around Caraça Ridge and employed in historical buildings in Brumal and Catas Altas do Mato Dentro, to name but a few. They can as well be kyanite-garnet-mica schists, with coloration ranging from green to bluish green, outcropping on Itacolomy Ridge, near Passagem de Mariana, or, simply, sericite schist from Santo Antônio Hill, in the same region. They can also be muscovite-chlorite-quartz schists with magnetite either dispersed or concentrated in thin bands, extracted around Ouro Preto and locally applied, or those used in buildings in São João d'El Rey and Tiradentes which were extracted from old quarries situated in the Candoga region, between Santa Cruz and Tiradentes, or from quarries in the Mangue region.

Witness of fluid-flow organization during high-pressure antigorite dehydration

NASA Astrophysics Data System (ADS)

López Sánchez-Vizcaíno, Vicente; Padrón-Navarta, José Alberto; Garrido, Carlos J.; Gómez-Pugnaire, María. Teresa

2010-05-01

The link between devolatilization reactions and fluid flow is crucial to unravel important geodynamic processes in subduction zones as deformation and element transfer is extremely controlled by the presence of water. At high confining pressure, significant fluid pressure gradients are expected in a reacting rock being dehydrated, because of its rather limited permeability [1]. Compactation-driven fluid flow seems to be an intrinsic mechanism occurring at devolatilization of viscolastic rocks. Nevertheless, and despite the important implications of this coupled deformation/fluid-migration mechanism for fluid transport, a conclusive confirmation of these processes by petrological and textural evidences in metamorphic terrains has been hampered by the scarcity of devolatilization fronts in the geological record. Evidences of high-pressure antigorite dehydration found at Cerro del Almirez (Betic Cordillera, Spain) [2] represent a noteworthy exception. Here, the transition between the hydrous protolith (antigorite serpentinite) and the prograde product assemblage (olivine + orthopyroxene + chlorite, chlorite harzburgite) is extremely well preserved and can be surveyed in detail. The maximum stability of the antigorite has been experimentally determined at ~680°C at 1.6-1.9 GPa [3]. Antigorite dehydration is accompanied by release of high amounts of high-pressure water-rich fluids (~ 9 wt.% fluid). Distinctive layers (up to 1 m thick) of transitional lithologies occur in between atg-serpentinite and chl-harburgite all along the devolatilization front, consisting of (1) chlorite-antigorite olivine-serpentinite, which gradually changes to (2) chlorite-antigorite-olivine-orthopyroxene serpentinite. These transitional lithologies are more massive and darker in color than atg-serpentinite and largely consist of coarse sized grains of antigorite and chlorite (250-500 μm). Antigorite in these assemblages is characterized by microstructural disorder features, which are lacking in antigorite far from the devolatilization front [4]. The sharp appearance of chlorite (Chl-in), crosscutting the serpentinite foliation, and coarsening of olivine define the upper limit of the transitional lithologies, whereas the lower limit (Atg-out) is gradational to chl-harzburgite. The modal increase of orthopyroxene is concomitant with the gradual disappearance of antigorite. The gradual disappearance of antigorite over short distances leads to the final prograde assemblage in the Chl-harzburgite with two contrasting textures: (1) coarse granular texture and (2) an intriguing spinifex-like texture (arborescent growth of centimeter-sized olivine and orthopyroxene). Both textures alternate at the meter to tens of meters scale over the entire massif. We interpret these textures as the result of contrasting pore fluid overpressure, reaction rates and fluid-flow organization shortly after the antigorite breakdown. These observations will be discussed on the frame of the reaction kinetic and the propagation of deformation associated to fluid pressure gradients. [1] Connolly, Journal of Geophysical Research 112 (B8), 18 (1997). [2] Trommsdorff, López Sánchez-Vizcaíno, Gómez-Pugnaire et al., Contrib Mineral Petr 132 (2), 139 (1998). [3] Padrón-Navarta, Hermann, Garrido et al., Contrib Mineral Petr 159 (1), 25 (2010). [4] Padrón-Navarta, López Sánchez-Vizcaíno, Garrido et al., Contrib Mineral Petr 156 (5), 679 (2008).

TRACE ELEMENT DISTRIBUTION IN SEDIMENTS OF THE MID-ATLANTIC RIDGE.

DTIC Science & Technology

MARINE GEOLOGY, ATLANTIC OCEAN), (*OCEAN BOTTOM, MINERALS), SEDIMENTATION, IRON, COBALT, MANGANESE, STRONTIUM, CHLORITES, NEUTRON ACTIVATION, GEOCHEMISTRY, CALCITE , CARBONATES, X RAY DIFFRACTION, CLAY MINERALS, THESES

Direct effect of chlorine dioxide, zinc chloride and chlorhexidine solution on the gaseous volatile sulfur compounds.

PubMed

Kim, Ju-Sik; Park, Ji-Woon; Kim, Dae-Jung; Kim, Young-Ku; Lee, Jeong-Yun

2014-11-01

This study focused on the ability of aqueous anti-volatile-sulfur-compound (VSC) solutions to eliminate gaseous VSCs by direct contact in a sealed space to describe possible mode of action of anti-VSC agents. Twenty milliliters of each experimental solution, 0.16% sodium chlorite, 0.25% zinc chloride, 0.1% chlorhexidine and distilled water, was injected into a Teflon bag containing mixed VSCs, hydrogen sulfide, methyl mercaptan and dimethyl sulfide and mixed vigorously for 30 s. The VSC concentration was measured by gas chromatography before, immediately after, 30 min and 60 min after mixing. The sodium chlorite solution reduced the VSC concentration remarkably. After mixing, nearly all VSCs were eliminated immediately and no VSCs were detected at 30 and 60 min post-mixing. However, in the other solutions, the VSC concentration decreased by ∼30% immediately after mixing and there was no further decrease. The results suggest that sodium chlorite solution has the effect of eliminating gaseous VSCs directly. This must be because it can release chlorine dioxide gas which can react directly with gaseous VSCs. In the case of other solutions that have been proved to be effective to reduce halitosis clinically, it can be proposed that their anti-VSC effect is less likely due to the direct chemical elimination of gaseous VSCs in the mouth.

Spectral properties and ASTER-based alteration mapping of Masahim volcano facies, SE Iran

NASA Astrophysics Data System (ADS)

Tayebi, Mohammad H.; Tangestani, Majid H.; Vincent, Robert K.; Neal, Devin

2014-10-01

This study applies Advanced Spaceborne Thermal Emission and Reflection Radiometer (ASTER) data and the Mixture Tuned Matched Filtering (MTMF) algorithm to map the sub-pixel distribution of alteration minerals associated with the Masahim volcano, SE Iran for understanding the spatial relationship between alteration minerals and volcano facies. Investigations of the alteration mineralogy were conducted using field-spectroscopy, X-ray diffraction (XRD) analysis and ASTER Short Wave Infrared (SWIR) spectral data. In order to spectrally characterize the stratovolcano deposits, lithological units and alteration minerals, the volcano was divided into three facies: the Central, Proximal, and Medial-distal facies. The reflectance spectra of rock samples show absorption features of a number of minerals including white mica, kaolinite, montmorillonite, illite, goethite, hematite, jarosite, opal, and chlorite. The end-members of key alteration minerals including sericite (phyllic zone), kaolinite (argillic zone) and chlorite (propylitic zone) were extracted from imagery using the Pixel Purity Index (PPI) method and were used to map alteration minerals. Accuracy assessment through field observations was used to verify the fraction maps. The results showed that most prominent altered rocks situated at the central facies of volcano. The alteration minerals were discriminated with the coefficient of determination (R2) of 0.74, 0.81, and 0.68 for kaolinite, sericite, and chlorite, respectively. The results of this study have the potential to refine the map of alteration zones in the Masahim volcano.

21 CFR 173.325 - Acidified sodium chlorite solutions.

Code of Federal Regulations, 2011 CFR

2011-04-01

... and processed root, tuber, bulb, legume, fruiting (i.e., eggplant, groundcherry, pepino, pepper... leafy vegetables (i.e., vegetables other than root, tuber, bulb, legume, fruiting, and cucurbit...

Chlorite dismutases, DyPs, and EfeB: 3 microbial heme enzyme families comprise the CDE structural superfamily

PubMed Central

Goblirsch, Brandon; Kurker, Richard C.; Streit, Bennett R.; Wilmot, Carrie M.; DuBois, Jennifer L.

2011-01-01

Heme proteins are extremely diverse, widespread, and versatile biocatalysts, sensors, and molecular transporters. The chlorite dismutase family of hemoproteins received its name due to the ability of the first-isolated members to detoxify anthropogenic ClO2−, a function believed to have evolved only in the last few decades. Family members have since been found in fifteen bacterial and archaeal genera, suggesting ancient roots. A structure- and sequence-based examination of the family is presented, in which key sequence and structural motifs are identified and possible functions for family proteins are proposed. Newly identified structural homologies moreover demonstrate clear connections to two other large, ancient, and functionally mysterious protein families. We propose calling them collectively the CDE superfamily of heme proteins. PMID:21354424

Chlorite Dissolution Rates From 25 to 275 degrees and pH 3 to 10

DOE Data Explorer

Carroll, Susan

2013-09-27

We have calculated a chlorite dissolution rate equation at far from equilibrium conditions by combining new data (20 experiments at high temperature) with previously published data Smith et al. 2013 and Lowson et al. 2007. All rate data (from the 127 experiments) are tabulated in this data submission. More information on the calculation of the rate data can be found in our FY13 Annual support (Carroll LLNL, 2013) which has been submitted to the GDR. The rate equation fills a data gap in geothemal kinetic data base and can be used directly to estimate the impact of chemical alteration on all geothermal processes. It is especially important for understanding the role of chemical alteration in the weakening for shear zones in EGS systems.

Mineralogy of parent rock and peaty-podzolic soil of Iremel Ridge, Southern Urals

NASA Astrophysics Data System (ADS)

Khalitov, R. M.; Perova, E. N.; Abakumov, E. V.; Suleimanov, R. R.

2017-08-01

The mineralogy of soils and parent rocks of the Iremel Ridge has been studied by the methods of micromorphology, laser diffraction, computed X-ray microtomography, and X-ray fluorescence analysis. In hard rock and soil, the major minerals have been identified: quartz, illite, and a chlorite-group mineral (Fe analogue of sudoite), as well as accessory minerals: monazite, xenotime, rutile, zircon, and florencite. It has been found that chlorite, illite, and quartz are present in all horizons of the studied peaty-podzolic soil. Insignificant amounts of mixed-layered mineral and kaolinite could be suggested in the T and EL horizons of peaty-podzolic soil. The mixed-layered mineral is most probably of soil origin, which is related to the transformation of illites inherited from the parent rock under acidic conditions.

Dissimilatory perchlorate reduction linked to aerobic methane oxidation via chlorite dismutase

NASA Astrophysics Data System (ADS)

Oremland, R. S.; Baesman, S. M.; Miller, L. G.

2013-12-01

The presence of methane (CH4) in the atmosphere of Mars is controversial yet the evidence has aroused scientific interest, as CH4 could be a harbinger of extant or extinct microbial life. There are various oxidized compounds present on the surface of Mars that could serve as electron acceptors for the anaerobic oxidation of CH4, including perchlorate (ClO4-). We examined the role of perchlorate, chlorate (ClO3-) and chlorite (ClO2-) as oxidants linked to CH4 oxidation. Dissimilatory perchlorate reduction begins with reduction of ClO4- to ClO2- and ends with dismutation of chlorite to yield chloride (Cl-) and molecular oxygen (O2). We explored the potential for aerobic CH4 oxidizing bacteria to couple with oxygen derived from chlorite dismutation during dissimilatory perchlorate reduction. Methane (0.2 kPa) was completely removed within several days from the N2-flushed headspace above cell suspensions of methanotrophs (Methylobacter albus strain BG8) and perchlorate reducing bacteria (Dechloromonas agitata strain CKB) in the presence of 5 mM ClO2-. Similar rates of CH4 consumption were observed for these mixed cultures whether they were co-mingled or segregated under a common headspace, indicating that direct contact of cells was not required for methane consumption to occur. We also observed complete removal of 0.2 kPa CH4 in bottles containing dried soil (enriched in methanotrophs by CH4 additions over several weeks) and D. agitata CKB and in the presence of 10 mM ClO2-. This soil (seasonally exposed sediment) collected from the shoreline of a freshwater lake (Searsville Lake, CA) demonstrated endogenous CH4 uptake as well as perchlorate, chlorate and chlorite reduction/dismutation. However, these experiments required physical separation of soil from the aqueous bacterial culture to allow for the partitioning of O2 liberated from chlorite dismutation into the shared headspace. Although dissimilatory reduction of ClO4- and ClO3- could be inferred from the accumulation of chloride ions either in spent media or in slurries prepared from Searsville Lake soil, neither of these oxyanions evoked methane oxidation when added to either anaerobic mixed cultures or soils enriched in methanotrophs. This result leads us to surmise that the release of O2 during enzymatic perchlorate reduction was low, and that the oxygen produced was unavailable to the aerobic methanotrophs. This was borne out by patterns of O2 and CO2 production during experiments with lake soil, growth media, and pure cultures of dissimilatory perchlorate reducing bacteria. We observed that O2 release during incubation of D. agitata CKB with 10 mM ClO4- or ClO3- was decoupled from metabolism. More O2 was released during incubations without added acetate than with 10 mM acetate and an even greater amount of O2 was released during incubation with heat-killed cells. This suggests a chemical mechanism of O2 production during reaction with ClO4- and ClO3-. Hence, perchlorate reducing bacteria need not be present to facilitate O2 release from the surface of Mars, in support of recent interpretations of Viking LR and GEx experiments.

21 CFR 173.300 - Chlorine dioxide.

Code of Federal Regulations, 2012 CFR

2012-04-01

... chlorate with hydrogen peroxide in the presence of sulfuric acid. (iii) Treating an aqueous solution of sodium chlorite by electrolysis. (2) The generator effluent contains at least 90 percent (by weight) of...

21 CFR 173.300 - Chlorine dioxide.

Code of Federal Regulations, 2013 CFR

2013-04-01

... chlorate with hydrogen peroxide in the presence of sulfuric acid. (iii) Treating an aqueous solution of sodium chlorite by electrolysis. (2) The generator effluent contains at least 90 percent (by weight) of...

Septate-tubular textures in 2.0-Ga pillow lavas from the Pechenga Greenstone Belt: a nano-spectroscopic approach to investigate their biogenicity.

PubMed

Fliegel, D; Wirth, R; Simonetti, A; Furnes, H; Staudigel, H; Hanski, E; Muehlenbachs, K

2010-12-01

Pillow lava rims and interpillow hyaloclastites from the upper part of the Pechenga Greenstone Belt, Kola Peninsula, N-Russia contain rare tubular textures 15-20 μm in diameter and up to several hundred μm long in prehnite-pumpellyite to lower greenschist facies meta-volcanic glass. The textures are septate with regular compartments 5-20 μm across and exhibit branching, stopping and no intersecting features. Synchrotron micro-energy dispersive X-ray was used to image elemental distributions; scanning transmission X-ray microscopy, Fe L-edge and C K-edge were used to identify iron and carbon speciation at interfaces between the tubular textures and the host rock. In situ U-Pb radiometric dating by LA-MC-ICP-MS (laser ablation multicollector inductively coupled plasma mass spectrometry) of titanite from pillow lavas yielded a metamorphic age of 1790 ± 89 Ma. Focused ion-beam milling combined with transmission electron microscopy was used to analyze the textures in three dimensions. Electron diffraction showed that the textures are mineralized by orientated pumpellyite. On the margins of the tubes, an interface between mica or chlorite and the pumpellyite shows evidence of dissolution reactions where the pumpellyite is replaced by mica/chlorite. A thin poorly crystalline Fe-phase, probably precipitated out of solution, occurs at the interface between pumpellyite and mica/chlorite. This sequence of phases leads to the hypothesis that the tubes were initially hollow, compartmentalized structures in volcanic glass that were mineralized by pumpellyite during low-grade metamorphism. Later, a Fe-bearing fluid mineralized the compartments between the pumpellyite and lastly the pumpellyite was partially dissolved and replaced by chlorite during greenschist metamorphism. The most plausible origin for a septate-tubular texture is a progressive etching of the host matrix by several generations of microbes and subsequently these tubes were filled by authigenic mineral precipitates. This preserves the textures in the rock record over geological time. The micro textures reported here thus represent a pumpellyite-mineralized trace fossil that records a Paleoproterozoic sub-seafloor biosphere. © 2010 Blackwell Publishing Ltd.

Telescoping metamorphic isograds: Evidence from 40Ar/39A dating in the Orange-Milford belt, southern Connecticut

USGS Publications Warehouse

Kunk, Michael J.; Walsh, Gregory J.; Growdon, Martha L.; Wintsch, Robert P.

2013-01-01

New 40Ar/39Ar ages for hornblende and muscovite from the Orange-Milford belt in southern Connecticut reflect cooling from Acadian amphibolite facies metamorphism between ∼380 to 360 Ma followed by retrograde recrystallization of fabric-forming muscovite and chlorite during lower greenschist facies Alleghanian transpression at ∼280 Ma. Reported field temperature and pressure gradients are improbably high for these rocks and a NW metamorphic field gradient climbing from chlorite-grade to staurolite-grade occurs over less than 5 km. Simple tilting cannot account for this compressed isograd spacing given the geothermal gradient of ∼20 °C/km present at the time of regional metamorphism. However, post-metamorphic transpression could effectively telescope the isograds by stretching the belt at an oblique angle to the isograd traces. Textures in the field and in thin section reveal several older prograde schistosities overprinted by lower greenschist facies fabrics. The late cleavages commonly occur at the scale of ∼100 μm and these samples contain multiple age populations of white mica. 40Ar/39Ar analysis of these poly-metamorphic samples with mixed muscovite populations yield climbing or U-shaped age spectra. The ages of the low temperature steps are late Paleozoic, while the ages of the older steps are late Devonian. These results support our petrologic interpretation that the younger cleavage developed under metamorphic conditions below the closure temperature for Ar diffusion in muscovite, that is, in the lower greenschist facies. The correlation of a younger regionally reproducible age population with a pervasive retrograde muscovite ± chlorite cleavage reveals an Alleghanian (∼280 Ma) overprint on the Acadian metamorphic gradient (∼380 Ma). Outcrop-scale structures including drag folds and imbricate boudins suggest that Alleghanian deformation and cleavage development occurred in response to dextral transpression along a northeast striking boundary. Alleghanian oblique collision of accreting terranes from the northeast would have resulted in northeast-southwest dextral transpression against the New York promontory. This deformation was responsible for crystallization of pervasive retrograde muscovite + chlorite cleavages and associated telescoping of the Acadian metamorphic isograds in southern Connecticut at ∼280 Ma.

Alteration and mineralization of an oceanic forearc and the ophiolite-ocean crust analogy

USGS Publications Warehouse

Alt, J.C.; Teagle, D.A.H.; Brewer, T.; Shanks, Wayne C.; Halliday, A.

1998-01-01

Mineralogical, chemical, and isotopic (O, C, S, and Sr) analyses were performed on minerals and bulk rocks from a forearc basement section to understand alteration processes and compare with mid-ocean ridges (MOR) and ophiolites. Ocean Drilling Program Hole 786B in the Izu-Bonin forearc penetrates 103 m of sediment and 725 m into volcanic flows, breccias, and basal dikes. The rocks comprise boninites and andesites to rhyolites. Most of the section was affected by low-temperature (<100??C) seawater alteration, with temperatures increasing downward. The rocks are partly (5-25%) altered to smectite, Fe-oxyhydroxide, calcite, and phillipsite, and exhibit gains of K, Rb, and P, loss of Ca, variable changes in Si, Na, Mg, Fe, Sr, and Y, and elevated ??18O and 87Sr/86Sr. Higher temperatures (???150??C) in the basal dikes below 750 m led to more intense alteration and formation of chlorite-smectite, corrensite, albite, K-feldspar, and quartz (??chlorite). A 5 m thick hydrothermally altered and pyritized zone at 815 m in the basal dikes reacted with mixtures of seawater and hydrothermal fluids to Mg-chlorite, albite, and pyrite, and gained Mg and S and lost Si and Ca. Focused flow of hydrothermal fluids produced sericitization halos (Na-K sericite, quartz, pyrophyllite, K-feldspar, and pyrite) along quartz veins at temperatures of 200??-250??C. High 87Sr/86Sr ratios of chloritized (???0.7055) and sericitized (???0.7065) rocks indicate involvement of seawater via mixing with hydrothermal fluids. Low ??34S of sulfide (???2 to -5.5???) and sulfate (12.5???) are consistent with input of magmatic SO2 into hydrothermal fluids and disproportionation to sulfide and sulfate. Alteration processes were generally similar to those at MORs, but the arc section is more intensively altered, in part because of the presence of abundant glassy rocks and mafic phases. The increase in alteration grade below 750 m and the mineralization in the basal dikes are analogous to changes that occur near the base of the volcanic section in MOR and the Troodos ophiolite.

21 CFR 173.300 - Chlorine dioxide.

Code of Federal Regulations, 2010 CFR

2010-04-01

... sodium chlorite by electrolysis. (2) The generator effluent contains at least 90 percent (by weight) of... Health Association, 800 I St. NW., Washington, DC 20001-3750. You may inspect a copy at the Center for...

HemQ: An iron-coproporphyrin oxidative decarboxylase for protoheme synthesis in Firmicutes and Actinobacteria

DOE PAGES

Dailey, Harry A.; Gerdes, Svetlana

2015-02-21

Genes for chlorite dismutase-like proteins are found widely among heme-synthesizing bacteria and some Archaea. It is now known that among the Firmicutes and Actinobacteria these proteins do not possess chlorite dismutase activity but instead are essential for heme synthesis. These proteins, named HemQ, are ironcoproporphyrin (coproheme) decarboxylases that catalyze the oxidative decarboxylation of coproheme III into protoheme IX. As purified, HemQs do not contain bound heme, but readily bind exogeneously supplied heme with low micromolar affinity. We find that the heme-bound form of HemQ has low peroxidase activity and in the presence of peroxide the bound heme may be destroyed.more » Furthermore, it is possible that HemQ may serve a dual role as a decarboxylase in heme biosynthesis and a regulatory protein in heme homeostasis.« less

Methane oxidation linked to chlorite dismutation

USGS Publications Warehouse

Miller, Laurence G.; Baesman, Shaun M.; Carlström, Charlotte I.; Coates, John D.; Oremland, Ronald S.

2014-01-01

We examined the potential for CH4 oxidation to be coupled with oxygen derived from the dissimilatory reduction of perchlorate, chlorate, or via chlorite (ClO−2) dismutation. Although dissimilatory reduction of ClO−4 and ClO−3 could be inferred from the accumulation of chloride ions either in spent media or in soil slurries prepared from exposed freshwater lake sediment, neither of these oxyanions evoked methane oxidation when added to either anaerobic mixed cultures or soil enriched in methanotrophs. In contrast, ClO−2 amendment elicited such activity. Methane (0.2 kPa) was completely removed within several days from the headspace of cell suspensions of Dechloromonas agitata CKB incubated with either Methylococcus capsulatus Bath or Methylomicrobium album BG8 in the presence of 5 mM ClO−2. We also observed complete removal of 0.2 kPa CH4 in bottles containing soil enriched in methanotrophs when co-incubated with D. agitata CKB and 10 mM ClO−2. However, to be effective these experiments required physical separation of soil from D. agitata CKB to allow for the partitioning of O2 liberated from chlorite dismutation into the shared headspace. Although a link between ClO−2 and CH4 consumption was established in soils and cultures, no upstream connection with either ClO−4 or ClO−3 was discerned. This result suggests that the release of O2 during enzymatic perchlorate reduction was negligible, and that the oxygen produced was unavailable to the aerobic methanotrophs.

Diagenetic contrast of sandstones in hydrocarbon prospective Mesozoic rift basins (Ethiopia, UK, USA)

NASA Astrophysics Data System (ADS)

Wolela, A.

2014-11-01

Diagenetic studied in hydrocarbon-prospective Mesozoic rift basins were carried out in the Blue Nile Basin (Ethiopia), Ulster Basin (United Kingdom) and Hartford Basin (United States of America). Alluvial fan, single and amalgamated multistorey meandering and braided river, deep and shallow perennial lake, shallow ephemeral lake, aeolian and playa mud-flat are the prominent depositional environments. The studied sandstones exhibit red bed diagenesis. Source area geology, depositional environments, pore-water chemistry and circulation, tectonic setting and burial history controlled the diagenetic evolution. The diagenetic minerals include: facies-related minerals (calcrete and dolocrete), grain-coating clay minerals and/or hematite, quartz and feldspar overgrowths, carbonate cements, hematite, kaolinite, illite-smectite, smectite, illite, chlorite, actinolite, laumontite, pyrite and apatite. Diversity of diagenetic minerals and sequence of diagenetic alteration can be directly related to depositional environment and burial history of the basins. Variation in infiltrated clays, carbonate cements and clay minerals observed in the studied sandstones. The alluvial fan and fluviatile sandstones are dominated by kaolinite, illite calcite and ferroan calcite, whereas the playa and lacustrine sandstones are dominated by illite-smectite, smectite-chlorite, smectite, chlorite, dolomite ferroan dolomite and ankerite. Albite, pyrite and apatite are predominantly precipitated in lacustrine sandstones. Basaltic eruption in the basins modified mechanically infiltrated clays to authigenic clays. In all the studied sandstones, secondary porosity predominates over primary porosity. The oil emplacement inhabited clay authigenesis and generation of secondary porosity, whereas authigenesis of quartz, pyrite and apatite continued after oil emplacement.

Paleozoic-Mesozoic boundary in the Berry Creek Quadrangle, northwestern Sierra Nevada, California

USGS Publications Warehouse

Hietanen, Anna Martta

1977-01-01

Structural and petrologic studies in the Berry Creek quadrangle at the north end of the western metamorphic belt of the Sierra Nevada have yielded new information that helps in distinguishing between the chemically similar Paleozoic and Mesozoic rocks. The distinguishing features are structural and textural and result from different degrees of deformation. Most Paleozoic rocks are strongly deformed and thoroughly recrystallized. Phenocrysts in meta volcanic rocks are granulated and drawn out into lenses that have sutured outlines. In contrast, the phenocrysts in the Mesozoic metavolcanic rocks show well-preserved straight crystal faces, are only slightly or not at all granulated, and contain fewer mineral inclusions than do those in the Paleozoic rocks. The groundmass in the Paleozoic rocks is recrystallized to a fairly coarse grained albite-epidote-amphibole-chlorite rock, whereas in the Mesozoic rocks the groundmass is a very fine grained feltlike mesh with only spotty occurrence of well-recrystallized finegrained albite-epidote-chlorite-actinolite rock. Primary minerals, such as augite, are locally preserved in the Mesozoic rocks but are altered to a mixture of amphibole, chlorite, and epidote in the Paleozoic rocks. In the contact aureoles of the plutons, and within the Big Bend fault zone, which crosses the area parallel to the structural trends, all rocks are thoroughly recrystallized and strongly deformed. Identification of the Paleozoic and Mesozoic rocks in these parts of the area was based on the continuity of the rock units in the field and on gradual changes in microscopic textures toward the plutons.

40 CFR 180.1070 - Sodium chlorite; exemption from the requirement of a tolerance.

Code of Federal Regulations, 2010 CFR

2010-07-01

... AGENCY (CONTINUED) PESTICIDE PROGRAMS TOLERANCES AND EXEMPTIONS FOR PESTICIDE CHEMICAL RESIDUES IN FOOD... agricultural practice as a seed-soak treatment in the growing of the raw agricultural commodities vegetable...

40 CFR 180.1070 - Sodium chlorite; exemption from the requirement of a tolerance.

Code of Federal Regulations, 2011 CFR

2011-07-01

... AGENCY (CONTINUED) PESTICIDE PROGRAMS TOLERANCES AND EXEMPTIONS FOR PESTICIDE CHEMICAL RESIDUES IN FOOD... agricultural practice as a seed-soak treatment in the growing of the raw agricultural commodities vegetable...

Fe-SAPONITE and Chlorite Growth on Stainless Steel in Hydrothermal Engineered Barrier Experiments

NASA Astrophysics Data System (ADS)

Cheshire, M. C.; Caporuscio, F. A.; McCarney, M.

2012-12-01

The United States recently has initiated the Used Fuel Disposition campaign to evaluate various generic geological repositories for the disposal of high-level, spent nuclear fuel within environments ranging from hard-rock, salt/clay, to deep borehole settings. Previous work describing Engineered Barrier Systems (EBS) for repositories focused on low temperature and pressure conditions. The focus of this experimental work is to characterize the stability and alteration of a bentonite-based EBS with different waste container materials in brine at higher heat loads and pressures. All experiments were run at ~150 bar and 125 to 300 C for ~1 month. Unprocessed bentonite from Colony, Wyoming was used in the experiments as the clay buffer material. The redox conditions for each system were buffered along the magnetite-iron oxygen fugacity univariant curve using Fe3O4 and Feo filings. A K-Na-Ca-Cl-based salt solution was chosen to replicate deep groundwater compositions. The experimental mixtures were 1) salt solution-clay; 2) salt solution -clay-304 stainless steel; and 3) salt solution -clay-316 stainless steel with a water/bentonite ratio of ~9. Mineralogy and aqueous geochemistry of each experiment was evaluated to monitor the reactions that took place. No smectite illitization was observed in these reactions. However, it appears that K-smectite was produced, possibly providing a precursor to illitization. It is unclear whether reaction times were sufficient for bentonite illitization at 212 and 300 C or whether conditions conducive to illite formation were obtained. The more notable clay mineral reactions occurred at the stainless steel surfaces. Authigenic chlorite and Fe-saponite grew with their basal planes near perpendicular to the steel plate, forming a 10 - 40 μm thick 'corrosion' layer. Partial dissolution of the steel plates was the likely iron source for chlorite/saponite formation; however, dissolution of the Feo/Fe3O4 may also have acted as an iron source, with the steel plates acting as a substrate for chlorite/saponite growth. Trace amounts of pyrite in the bentonite appeared to have reacted to form H2S gas and pentlandite ((Ni,Fe)8S9). Mineral growth on the waste containers was influenced by the container, buffer, and fluid compositions, in addition to pressure and temperature conditions. No significant mineralogical changes were apparent away from the steel-smectite interface. Results of this research show that the waste container may act as a substrate for mineral growth in response to corrosion. However, it is presently unknown whether chlorite and Fe-saponite will act as passivating agents or whether their presence will facilitate further corrosion of the waste containers. The role of these Fe-rich minerals on the stability of steel canisters at elevated heat loads is currently under investigation. LA-UR-12-23845

Unlocking the Secrets of the Mantle Wedge: New Insights Into Melt Generation Processes in Subduction Zones

NASA Astrophysics Data System (ADS)

Grove, T. L.

2007-05-01

Recent laboratory studies of the melting and crystallization behavior of mantle peridotite and subduction zone lavas have led to new insights into melting processes in island arc settings. Melting of the mantle wedge in the presence of H2O begins at much lower temperatures than previously thought. The solidus of mantle peridotite at 3 GPa is ~ 800 °C, which is 200 °C below previous estimates. At pressures greater than 2.4 GPa chlorite becomes a stable phase on the solidus and it remains stable until ~ 3.5 GPa. Therefore, melting over this pressure range occurs in the presence of chlorite, which contains ~ 12 wt. % H2O. Chlorite stabilized on the peridotite solidus by slab-derived H2O may be the ultimate source of H2O for subduction zone magmatism. Thus, chlorite could transport large amounts of H2O into the descending mantle wedge to depths where it can participate in melting to generate hydrous arc magmas. Our ability to identify primitive mantle melts at subduction zones has led to the following observations. 1) Primitive mantle melts show evidence of final equilibration at shallow depths near the mantle - crust boundary. 2) They contain variable amounts of dissolved H2O (up to 6 wt. %). 3) They record variable extents of melting (up to > 25 wt. %). To produce melts with such variable characteristics requires more than one melting process and requires consideration of a new type of melting called hydrous flux melting. Flux melting occurs when the H2O - rich melt initially produced on the solidus near the base of the mantle wedge ascends and continuously reacts with overlying hotter, shallower mantle. The mantle melts and magmatic H2O content is constantly diluted as the melt ascends and reacts with shallower, hotter mantle. Anhydrous mantle melts are also found in close temporal and spatial proximity to hydrous flux melts. These melts are extracted at similar depths near the top of the mantle wedge when mantle is advected up and into the wedge corner and melted by adiabatic decompression. In light of these new insights into the chemical processes that lead to melt generation in subduction zones, further study of the influence of mantle dynamics and physical processes on melting is crucial. Variations in mantle permeability near the base of the wedge may exercise important controls on the access of fluids and/or melts to the overlying wedge. The presence of chlorite in the wedge may also influence rheological properties and seismicity in the vicinity of the slab - wedge interface. Improved knowledge of rheology and permeability will help us to develop more robust models of mantle flow and temperature distribution in the mantle wedge. These are crucial for refining melting models. By combining evidence from petrology, geochemistry and geophysics the mysteries that attend the generation of melt in the mantle wedge can be resolved.

40 CFR 141.53 - Maximum contaminant level goals for disinfection byproducts.

Code of Federal Regulations, 2014 CFR

2014-07-01

... byproduct MCLG(mg/L) Bromodichloromethane zero Bromoform zero Bromate zero Chlorite 0.8 Chloroform 0.07 Dibromochloromethane 0.06 Dichloroacetic acid zero Monochloroacetic acid 0.07 Trichloroacetic acid 0.02 [63 FR 69465...

40 CFR 141.53 - Maximum contaminant level goals for disinfection byproducts.

Code of Federal Regulations, 2012 CFR

2012-07-01

... byproduct MCLG(mg/L) Bromodichloromethane zero Bromoform zero Bromate zero Chlorite 0.8 Chloroform 0.07 Dibromochloromethane 0.06 Dichloroacetic acid zero Monochloroacetic acid 0.07 Trichloroacetic acid 0.02 [63 FR 69465...

40 CFR 141.53 - Maximum contaminant level goals for disinfection byproducts.

Code of Federal Regulations, 2011 CFR

2011-07-01

... byproduct MCLG(mg/L) Bromodichloromethane zero Bromoform zero Bromate zero Chlorite 0.8 Chloroform 0.07 Dibromochloromethane 0.06 Dichloroacetic acid zero Monochloroacetic acid 0.07 Trichloroacetic acid 0.02 [63 FR 69465...

40 CFR 141.53 - Maximum contaminant level goals for disinfection byproducts.

Code of Federal Regulations, 2013 CFR

2013-07-01

... byproduct MCLG(mg/L) Bromodichloromethane zero Bromoform zero Bromate zero Chlorite 0.8 Chloroform 0.07 Dibromochloromethane 0.06 Dichloroacetic acid zero Monochloroacetic acid 0.07 Trichloroacetic acid 0.02 [63 FR 69465...

Geology and hydrothermal alteration at the Madh adh Dhahab epithermal precious-metal deposit, Kingdom of Saudi Arabia

USGS Publications Warehouse

Doebrich, J.L.; LeAnderson, J.P.

1984-01-01

Vein-related alteration consisting of quartz-sericite-pyrite, chloritic, argillic, and silicic halos was superimposed on broad zones of pervasive silicic, potassic, and argillic alteration that surrounds the rhyolite intrusive body. Quartz-sericite-pyrite alteration associated with the earliest stage of mineralization was followed by broad, pervasive, stratigraphically controlled potassic alteration. Subsequent mineralization was accompanied by quartz-sericitepyrite alteration and was followed by the main stage of mineralization that formed strong chloritic alteration halos. Development of broad zones and halos of argillic alteration also may have been related to the main stage of mineralization. Development of silicic halos was characteristic of the late stages of mineralization. Broad, pervasive propylitic alteration was then superimposed on all alteration types and represents cooling and inward encroachment of the hydrothermal system. All alteration, except the early silicic alteration is interpreted to have been related to circulating meteoric fluids heated by the rhyolite.

Mineralogy and geochemistry of the Lower Cretaceous siliciclastic rocks of the Morita Formation, Sierra San José section, Sonora, Mexico

NASA Astrophysics Data System (ADS)

Madhavaraju, J.; Pacheco-Olivas, S. A.; González-León, Carlos M.; Espinoza-Maldonado, Inocente G.; Sanchez-Medrano, P. A.; Villanueva-Amadoz, U.; Monreal, Rogelio; Pi-Puig, T.; Ramírez-Montoya, Erik; Grijalva-Noriega, Francisco J.

2017-07-01

Clay mineralogy and geochemical studies were carried out on sandstone and shale samples collected from the Sierra San José section of the Morita Formation to infer the paleoclimate and paleoweathering conditions that prevailed in the source region during the deposition of these sediments. The clay mineral assemblages (fraction < 2 μm) of the Sierra San José section are composed of chlorite and illite. The abundance of illite and chlorite in the studied samples suggest that the physical weathering conditions were dominant over chemical weathering. Additionally, the illite and chlorite assemblages reflect arid or semi-arid climatic conditions in the source regions. K2O/Al2O3 ratio of shales vary between 0.15 and 0.26, which lie in the range of values for clay minerals, particularly illite composition. Likewise, sandstones vary between 0.06 and 0.13, suggesting that the clay minerals are mostly kaolinte and illite types. On the chondrite-normalized diagrams, sandstone and shale samples show enriched light rare earth elements (LREE), flat heavy rare earth elements (HREE) patterns and negative Eu anomalies. The CIA and PIA values and A-CN-K plot of shales indicate low to moderate degree of weathering in the source regions. However, the sandstones have moderate to high values of CIA and PIA suggesting a moderate to intense weathering in the source regions. The SiO2/Al2O3 ratios, bivariate and ternary plots, discriminant function diagram and elemental ratios indicate the felsic source rocks for sandstone and shale of the Morita Formation.

Algal toxicity of the alternative disinfectants performic acid (PFA), peracetic acid (PAA), chlorine dioxide (ClO2) and their by-products hydrogen peroxide (H2O2) and chlorite (ClO2-).

PubMed

Chhetri, Ravi Kumar; Baun, Anders; Andersen, Henrik Rasmus

2017-05-01

Environmental effect evaluation of disinfection of combined sewer overflow events with alternative chemical disinfectants requires that the environmental toxicity of the disinfectants and the main by-products of their use are known. Many disinfectants degrade quickly in water which should be included in the evaluation of both their toxicity as determined in standardized tests and their possible negative effect in the water environment. Here we evaluated according to the standardized ISO 8692 test the toxicity towards the green microalgae, Pseudokirchneriella subcapitata, of three disinfectants: performic acid (PFA), peracetic acid (PAA) and chlorine dioxide (ClO 2 ) as well as two by-products of their use: hydrogen peroxide (H 2 O 2 ) and chlorite. All of the five chemicals investigated showed clear toxicity to the algae with well-defined dose response curves. The EC 50 values ranged from 0.16 to 2.9mg/L based on nominal concentrations leading to the labeling of the chemicals as either toxic or very toxic. The five investigated chemicals decreased in toxicity in the order chlorine dioxide, performic acid, peracetic acid, chlorite and hydrogen peroxide. The stability of the chemicals increased in the same order as the toxicity decrease. This indicates that even though ClO 2 has the highest environmental hazard potential, it may still be suitable as an alternative disinfectant due to its rapid degradation in water. Copyright © 2016 Elsevier GmbH. All rights reserved.

Geochemistry of volcanogenic clayey marine sediments from the Hazar-Maden Basin (Eastern Turkey)

NASA Astrophysics Data System (ADS)

Akkoca, Dicle Bal; Kürüm, Sevcan; Huff, Warren D.

2013-12-01

The Hazar-Madeıı Basin sediments were deposited along the southern branch of the Neotethys Ocean margin during Late Maastrichtian-Middle Eocene times. X-ray powder diffraction (XRD), ICP-AES, ICP-MS and scanning electron microscopy (SEM) were performed on samples of the Upper Maastrichtian-Middle Eocene Hazar Group and the Middle Eocene Maden Complex from the Hazar-Maden Basin to investigate the main effects of depositional envi- ronmental parameters in three sections belonging to deeper marine (slope), proximal arc volcanic (Mastarhill and Yukaribag sections) and shallow platform marine (Sebken section) settings. Marine sediments contain clay minerals (smectite, smectite/chlorite, chlorite, illite, interstratified illite/smectite, illite/chlorite, palygorskite), clinoptilolite, quartz, feldspar, calcite, dolomite, opal-CT and hematite. The clays are dominated by iron-rich smectites. La, Zr and Th concentrations are high in the shallow marginal Sebken section where the terrestrial detrital contribution is significant, while Sc and Co are more dominant in the deeper marine (slope) Yukaribag section, which is represented by basic-type volcanism and a higher contribution of hydrothermal phases. In a chondrite-normalized REE diagram, the negative Eu anomaly in samples from Sebken, the section which was deposited in a shallow marine environment, is less significant than that of the other two sections indicating the presence of a high terrestrial contribution in that part of the basin. A decrease in LREE v/HREEiV and Lajv/Ybv, LaiV/Sin v ratios from Sebken to Mastarhill and the Yukaribag sections indi- cates deepening of the basin and an increasing contribution of volcanism in that direction.

40 CFR 141.132 - Monitoring requirements.

Code of Federal Regulations, 2011 CFR

2011-07-01

... discretion. (2) Chlorite. Community and nontransient noncommunity water systems using chlorine dioxide, for... samples. (ii) Reduced monitoring. Monitoring may not be reduced. (2) Chlorine dioxide—(i) Routine... three chlorine dioxide distribution system samples. If chlorine dioxide or chloramines are used to...

Uranium speciation as a function of depth in contaminated hanford sediments--a micro-XRF, micro-XRD, and micro- and bulk-XAFS study.

PubMed

Singer, David M; Zachara, John M; Brown, Gordon E

2009-02-01

The distribution and speciation of U and Cu in contaminated vadose zone and aquifer sediments from the U.S. DOE Hanford site (300 Area) were determined using a combination of synchrotron-based micro-X-ray fluorescence (microXRF) imaging, micro-X-ray absorption near edge structure (microXANES) spectroscopy, and micro-X-ray diffraction (microXRD) techniques combined with bulk U LIII-edge X-ray absorption fine structure (XAFS) spectroscopy. Samples were collected from within the inactive North Process Pond (NPP2) at 8 ft (2.4 m, NPP2-8) depth and 12 ft (3.7 m, NPP2-12) depth in the vadose zone, and fines were isolated from turbid groundwater just below the water Table (12-14 ft, approximately 4 m, NPP2-GW). microXRF imaging, microXRD, and microXANES spectroscopy revealed two major U occurrences within the vadose and groundwater zones: (1) low to moderate concentrations of U(VI) associated with fine-textured grain coatings that were consistently found to contain clinochlore (referred to here as chlorite) observed in all three samples, and (2) U(VI)-Cu(II) hotspots consisting of micrometer-sized particles associated with surface coatings on grains of muscovite and chlorite observed in samples NPP2-8' and NPP2-GW. In the aquifer fines (NPP2-GW), these particles were identified as cuprosklodowskite (cps: Cu[(UO2)(SiO2OH)]2 x 6H2O) and metatorbernite (mtb: Cu(UO2)2(PO4)2 x 8H2O). In contrast, the U-Cu-containing particles in the vadose zone were X-ray amorphous. Analyses of U LIII-edge XAFS spectra by linear-combination fitting indicated that U speciation consisted of (1) approximately 75% uranyl sorbed to chlorite and approximately 25% mtb-like X-ray amorphous U-Cu-phosphates (8 ft depth), (2) nearly 100% sorbed uranyl (12 ft depth), and (3) approximately 70% uranyl sorbed to chlorite and approximately 30% cps/mtb (groundwater zone). These findings suggest that dissolution of U(VI)-Cu(II)-bearing solids as well as desorption of U(VI), mainly from phyllosilicates, are important persistent sources of U(VI) to the associated uranium groundwater plume in Hanford Area 300.

Microstructures Indicate Large Influence of Temperature and Fluid Pressure on the Reactivation of the Alpine Fault, New Zealand

NASA Astrophysics Data System (ADS)

Schuck, B.; Janssen, C.; Schleicher, A.; Toy, V.; Dresen, G.

2017-12-01

The transpressional Alpine Fault within New Zealand's South Island is the major structure that accommodates relative motion between the Pacific and the Australian Plates. It has been intensively studied, because it is late in its 291-year seismic cycle (Cochran et al., 2017; doi: 10.1016/j.epsl.2017.02.026), is likely to generate large (i.e. MW > 8) earthquakes, thus presents the biggest seismic hazard in the region. However, because it is severely misoriented in the present-day stress field for reactivation (Boese et al., 2013; doi: 10.1016/j.epsl.2013.06.030), supra-lithostatic fluid-pressures are required for rupture nucleation. We have analyzed microstructures (SEM and TEM), geochemistry (ICP-OES) and mineralogy (XRD) of outcrop samples of the fault core to investigate the influence of fluids on the geomechanical behavior of the fault. Fluid-related alteration is pervasive within 20 m of the principal slip zone (PSZ) (Sutherland et al., 2012; doi: 10.1130/G33614.1), which is an incohesive, cemented and repeatedly reworked fault gouge mostly consisting of a fine-grained matrix composed of comminuted detrital quartz and feldspar as well as authigenic chlorite and calcite. Authigenic phases seal the PSZ for interseismic cross-fault fluid flow and enable fluid pressure to build-up. Notable, smectite, previously considered to significantly influence propagation of Alpine Fault ruptures, is not present in these samples. Undeformed, euhedral chlorite grains suggest that the processes leading to fault sealing are not only active at greater depths but also close to the surface. The absence of smectite and the presence of undeformed chlorite at very shallow depths can be attributed to the fault's high geothermal gradient of > 120 °C km-1 (Sutherland et al., 2012; doi:10.1038/nature22355), which gives temperature conditions unfavorable for smectite to be stable and fostering chlorite growth. A pervasive network of anastomosing calcite veins in the fault core, depicting mutual cross-cutting relations, attests for episodic fluid flow and mineralization within the PSZ. We interpret these as microstructural evidence for transient fault core permeability resulting from rupture nucleation due to supra-lithostatic fluid pressures following during fault-valve behavior.

Metamorphic mineral assemblages of slightly calcic pelitic rocks in and around the Taconic Allochthon, southwestern Massachusetts and adjacent Connecticut and New York

USGS Publications Warehouse

Zen, E-an

1981-01-01

The mineral assemblages from metamorphosed slightly calcic pelitic rocks of the Taconic Range in southwestern Massachusetts and adjacent areas of Connecticut and New York were studied petrographically and chemically. These rocks vary in metamorphic grade from those below the chloritoid zone through the chloritoid and garnet zones into the kyanite-staurolite zone. Microprobe data on the ferromagnesian minerals show that the sequence of increasing Fe/ (Fe+Mg) value is, from the lowest, chlorite, biotite, hornblende, chloritoid, staurolite, garnet. Hornblende, epidote, garnet, and plagioclase are the most common minerals that carry significant calcium. Biotite is persistently deficient in alkali but is abnormally rich in octahedral aluminum to such an extent that the overall charge balance can be ascribed to an AI=K+ (Fe,Mg) diadochy. Muscovite contains small though persistent amounts of iron and magnesium in octahedral positions but has a variable K/Na ratio, which is potentially useful as a geothermometer. One low-grade muscovite is highly phengitic, but the white micas in rocks from metamorphic grades higher than chloritoid zone do not contain significant phengite components. Chlorite is persistently high in aluminum and so its ratio of divalent ions to aluminum is approximately that of garnet. Many garnets show pronounced zoning in manganese and less pronounced zoning in calcium. Garnet coexisting with hornblende contains a high proportion of the grossularitic component. The calcium content is significant in all the analyzed garnets, except those from a cummingtonite-bearing sample that is free of muscovite. This suggests that in slightly calcic pelitic rocks, calcium-free garnet cannot coexist with muscovite. Most of the mineral assemblages formed in the presence of excess quartz and muscovite. The phase-petrologic analysis, made with the aid of an eight-phase multisystematic model, shows the following major points: 1. Chloritoid and staurolite coexist in a definite interval of prograde metamorphism. 2. Biotite-chloritoid does not constitute an alternative assemblage to garnet-chlorite-muscovite, because the former combination is found predominantly in the presence of the latter combination. Because the garnet contains lime, all five phases are stable together in lowlime pelitic rocks. 3. The first appearance of staurolite in the area does not correspond to the reaction leading to the first intrinsic stable existence of this phase. Inasmuch as the first appearanc,e of staurolite is always in chlorite-bearing as semblages, I suggest that the mapped staurolite zone marker corresponds to a reaction whereby staurolitechlorite becomes stable. The probable lower grade chemical equivalent, for example, chloritoid-aluminum silicate, however, has not been found in the area of study. Several staurolite-forming reactions discussed in the literature are ruled out because of the relative siderophility of the minerals. A second staurolite isograd involves the reaction, chloritoid+chlorite+muscovite= staurolite+biotite. A third isograd involves staurolite+ chlorite=biotite+kyanite; this reaction is postulated on the basis of the observed assemblage biotite-kyanitesta urolite-garnet-muscoviteplagioclase-quartzilmenite. 4. In low-grade rocks, epidote is stable considerably before the first appearance of chloritoid. The nature of the high-aluminum phase in low-grade rocks that leads to the formation of chloritoid remains obscure. The epidote is always rich in ferric iron (pistacite content of about 1/ 4 to 1/3). Garnet-bearing assemblages (with or without epidote) are formed next as metamorphic grade increases. The next more calcium-rich silicate is hornblende, and despite the meager data on assemblages that include hornblende, the first intrinsic appearance of this phase has probably been recorded. At highstaurolite grade, the most calcium-rich assemblage in pelitic rocks is hornblende-garnet-biotite-plagioclase (bytownit

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

NASA Astrophysics Data System (ADS)

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.

Disinfection by-products of chlorine dioxide (chlorite, chlorate, and trihalomethanes): Occurrence in drinking water in Qatar.

PubMed

Al-Otoum, Fatima; Al-Ghouti, Mohammad A; Ahmed, Talaat A; Abu-Dieyeh, Mohammed; Ali, Mohammed

2016-12-01

The occurrence of chlorine dioxide (ClO 2 ) disinfection by-products (DBPs) in drinking water, namely, chlorite, chlorate, and trihalomethanes (THMs), was investigated. Two-hundred-ninety-four drinking water samples were collected from seven desalination plants (DPs), four reservoirs (R), and eight mosques (M) distributed within various locations in southern and northern Qatar. The ClO 2 concentration levels ranged from 0.38 to <0.02 mg L -1 , with mean values of 0.17, 0.12, and 0.04 mg L -1 for the DPs, Rs, and Ms, respectively. The chlorite levels varied from 13 μg L -1 to 440 μg L -1 , with median values varying from 13 to 230 μg L -1 , 77-320 μg L -1 , and 85-440 μg L -1 for the DPs, Rs, and Ms, respectively. The chlorate levels varied from 11 μg L -1 to 280 μg L -1 , with mean values varying from 36 to 280 μg L -1 , 11-200 μg L -1 , and 11-150 μg L -1 in the DPs, Rs, and Ms, respectively. The average concentration of THMs was 5 μg L -1 , and the maximum value reached 77 μg L -1 However, all of the DBP concentrations fell within the range of the regulatory limits set by GSO 149/2009, the World Health Organization (WHO), and Kahramaa (KM). Copyright © 2016 Elsevier Ltd. All rights reserved.

Link between Indian monsoon rainfall and physical erosion in the Himalayan system during the Holocene

NASA Astrophysics Data System (ADS)

Joussain, Ronan; Liu, Zhifei; Colin, Christophe; Duchamp-Alphonse, Stéphanie; Yu, Zhaojie; Moréno, Eva; Fournier, Léa.; Zaragosi, Sébastien; Dapoigny, Arnaud; Meynadier, Laure; Bassinot, Franck

2017-09-01

Mineralogical and geochemical analyses conducted on cores located on the active channel-levee system of the northern Bengal Fan are used to establish changes in the weathering pattern and the sediment transport of the Himalayan system, and evaluate the effect of Indian summer monsoon rainfall during the Holocene. Our data indicate that during the Holocene, sediments from the northern Bengal Fan originate mainly from the G-B river system without any significant changes in the relative contribution of these rivers. From 9.8 to around 6 ka, relatively low smectite/(illite+chlorite) ratios and relatively high K/Si* ratios indicate high physical denudation rates of the Himalayan highlands together with a rapid transfer of the detrital material to the Bengal Fan. The period between 9.2 and 7 ka is associated to lower values of K/Si* and corresponds to the maximum of Indian monsoon rainfall which indicates a more important chemical weathering material that rapidly transits by the G-B river system without a long storage in the Indo-Gangetic plain. From 6.0 ka to present day, higher smectite/(illite+chlorite) ratio and lower K/Si* ratio document a gradual increase of sediments originated from the Indo-Gangetic plain, characterized by higher degree of chemical weathering. During the last 2.5 ka, the drastic increase in the smectite/(illite+chlorite) ratio could be associated to enhanced alteration of the plain soils due to anthropogenic activity. The comparison of mineralogical and geochemical data with previous reconstructions of the Indian monsoon dynamic indicates a rapid response of erosion and sediment transfer of the G-B river system to changes of monsoon rainfall intensity.

High-affinity nitrate/nitrite transporters NrtA and NrtB of Aspergillus nidulans exhibit high specificity and different inhibitor sensitivity

PubMed Central

Akhtar, Naureen; Karabika, Eugenia; Kinghorn, James R.; Glass, Anthony D.M.; Unkles, Shiela E.

2015-01-01

The NrtA and NrtB nitrate transporters are paralogous members of the major facilitator superfamily in Aspergillus nidulans. The availability of loss-of-function mutations allowed individual investigation of the specificity and inhibitor sensitivity of both NrtA and NrtB. In this study, growth response tests were carried out at a growth-limiting concentration of nitrate (1 mM) as the sole nitrogen source, in the presence of a number of potential nitrate analogues at various concentrations, to evaluate their effect on nitrate transport. Both chlorate and chlorite inhibited fungal growth, with chlorite exerting the greater inhibition. The main transporter of nitrate, NrtA, proved to be more sensitive to chlorate than the minor transporter, NrtB. Similarly, the cation caesium was shown to exert differential effects, strongly inhibiting the activity of NrtB, but not NrtA. In contrast, no inhibition of nitrate uptake by NrtA or NrtB transporters was observed in either growth tests or uptake assays in the presence of bicarbonate, formate, malonate or oxalate (sulphite could not be tested in uptake assays owing to its reaction with nitrate), indicating significant specificity of nitrate transport. Kinetic analyses of nitrate uptake revealed that both chlorate and chlorite inhibited NrtA competitively, while these same inhibitors inhibited NrtB in a non-competitive fashion. The caesium ion appeared to inhibit NrtA in a non-competitive fashion, while NrtB was inhibited uncompetitively. The results provide further evidence of the distinctly different characteristics as well as the high specificity of nitrate uptake by these two transporters. PMID:25855763

Controlled clinical evaluations of chlorine dioxide, chlorite and chlorate in man.

PubMed Central

Lubbers, J R; Chauan, S; Bianchine, J R

1982-01-01

To assess the relative safety of chronically administered chlorine water disinfectants in man, a controlled study was undertaken. The clinical evaluation was conducted in the three phases common to investigational drug studies. Phase I, a rising dose tolerance investigation, examined the acute effects of progressively increasing single doses of chlorine disinfectants to normal healthy adult male volunteers. Phase II considered the impact on normal subjects of daily ingestion of the disinfectants at a concentration of 5 mg/l. for twelve consecutive weeks. Persons with a low level of glucose-6-phosphate dehydrogenase may be expected to be especially susceptible to oxidative stress; therefore, in Phase III, chlorite at a concentration of 5 mg/l. was administered daily for twelve consecutive weeks to a small group of potentially at-risk glucose-6-phosphate dehydrogenase-deficient subjects. Physiological impact was assessed by evaluation of a battery of qualitative and quantitative tests. The three phases of this controlled double-blind clinical evaluation of chlorine dioxide and its potential metabolites in human male volunteer subjects were completed uneventfully. There were no obvious undesirable clinical sequellae noted by any of the participating subjects or by the observing medical team. In several cases, statistically significant trends in certain biochemical or physiological parameters were associated with treatment; however, none of these trends was judged to have physiological consequence. One cannot rule out the possibility that, over a longer treatment period, these trends might indeed achieve proportions of clinical importance. However, by the absence of detrimental physiological responses within the limits of the study, the relative safety of oral ingestion of chlorine dioxide and its metabolites, chlorite and chlorate, was demonstrated. PMID:6961033

Clay Mineralogy of AN Alluvial Aquifer in a Mountainous, Semiarid Terrain, AN Example from Rifle, Colorado

NASA Astrophysics Data System (ADS)

Elliott, W. C.; Lim, D.; Zaunbrecher, L. K.; Pickering, R. A.; Williams, K. H.; Navarre-Sitchler, A.; Long, P. E.; Noel, V.; Bargar, J.; Qafoku, N. P.

2015-12-01

Alluvial sediments deposited along the Colorado River corridor in the semi-arid regions of central to western Colorado can be important hosts for legacy contamination including U, V, As and Se. These alluvial sediments host aquifers which are thought to provide important "hot spots" and "hot moments" for microbiological activity controlling organic carbon processing and fluxes in the subsurface. Relatively little is known about the clay mineralogy of these alluvial aquifers and the parent alluvial sediments in spite of the fact that they commonly include lenses of silt-clay materials. These lenses are typically more reduced than coarser grained materials, but zones of reduced and more oxidized materials are present in these alluvial aquifer sediments. The clay mineralogy of the non-reduced parent alluvial sediments of the alluvial aquifer located in Rifle, CO (USA) is composed of chlorite, smectite, illite, kaolinite and quartz. The clay mineralogy of non-reduced fine-grained materials at Rifle are composed of the same suite of minerals found in the sediments plus a vermiculite-smectite intergrade that occurs near the bottom of the aquifer near the top of the Wasatch Formation. The clay mineral assemblages of the system reflect the mineralogically immature character of the source sediments. These assemblages are consistent with sediments and soils that formed in a moderately low rainfall climate and suggestive of minimal transport of the alluvial sediments from their source areas. Chlorite, smectite, smectite-vermiculite intergrade, and illite are the likely phases involved in the sorption of organic carbon and related microbial redox transformations of metals in these sediments. Both the occurrence and abundance of chlorite, smectite-vermiculite, illite and smectite can therefore exert an important control on the contaminant fluxes and are important determinants of biogeofacies in mountainous, semiarid terrains.

High-temperature quartz cement and the role of stylolites in a deep gas reservoir, Spiro Sandstone, Arkoma Basin, USA

USGS Publications Warehouse

Worden, Richard H.; Morad, Sadoon; Spötl, C.; Houseknecht, D.W.; Riciputi, L.R.

2000-01-01

The Spiro Sandstone, a natural gas play in the central Arkoma Basin and the frontal Ouachita Mountains preserves excellent porosity in chloritic channel-fill sandstones despite thermal maturity levels corresponding to incipient metamorphism. Some wells, however, show variable proportions of a late-stage, non-syntaxial quartz cement, which post-dated thermal cracking of liquid hydrocarbons to pyrobitumen plus methane. Temperatures well in excess of 150°C and possibly exceeding 200°C are also suggested by (i) fluid inclusions in associated minerals; (ii) the fact that quartz post-dated high-temperature chlorite polytype IIb; (iii) vitrinite reflectance values of the Spiro that range laterally from 1.9 to ≥ 4%; and (iii) the occurrence of late dickite in these rocks. Oxygen isotope values of quartz cement range from 17.5 to 22.4‰ VSMOW (total range of individual in situ ion microprobe measurements) which are similar to those of quartz cement formed along high-amplitude stylolites (18.4–24.9‰). We favour a model whereby quartz precipitation was controlled primarily by the availability of silica via deep-burial stylolitization within the Spiro Sandstone. Burial-history modelling showed that the basin went from a geopressured to a normally pressured regime within about 10–15 Myr after it reached maximum burial depth. While geopressure and the presence of chlorite coats stabilized the grain framework and inhibited nucleation of secondary quartz, respectively, stylolites formed during the subsequent high-temperature, normal-pressured regime and gave rise to high-temperature quartz precipitation. Authigenic quartz growing along stylolites underscores their role as a significant deep-burial silica source in this sandstone.

Mass changes during hydrothermal alteration/mineralization in the gold-bearing Astaneh granitoid, western Iran

NASA Astrophysics Data System (ADS)

Zahra Afshooni, Seyedeh; Esmaeily, Dariush

2010-05-01

The Astaneh granitoid massif, located in western Iran, is a part of Sanandaj-Sirjan structural Zone. This body, mainly consist of granodioritic rocks, is widely affected under hydrothermal alteration and four alteration zones including phyllic (sericitic), chloritic, propylitic and argillic zones could be identified in this area. Four main mineralization- related alteration episodes have been studied in terms of mass transfer and element mobility during the hydrothermal evolution of Astaneh deposit. In order to illustrate these changes quantitatively, isocon plots have been applied. Isocon plots illustrate that Al, Ti, Ga and Tm was relatively immobile during alteration and that mass were essentially conserved during alteration. Phyllic alteration was accompanied by the depletion of Na and Fe and the enrichment of Si and Cu. The loss of Na and Fe reflects the sericitization of alkali feldspar and the destruction of ferromagnesian minerals. The addition of Si is consistent with widespread silicification wich is a major feature of phyllic alteration. All of the HFSE (except in Y), were enriched but all REEs were depleted in this zone. The overall obtained results show that major oxides such as SiO2, Al2O3, Fe2O3, MnO, MgO, CaO, Na2O, K2O, P2O5 and TiO2 and also LOI show dissimilar behaviors in the different zones. All of the LFSE, HFSE and FTSM (except in Cu and Mo) were depleted in argillic alteration but show dissimilar behaviors in the other alteration zones. The results shown strong depletion in REE, in particular LREE, in all of the alteration facies (except in chloritic zone), equivalent fresh rocks. In chloritic zone, compared with HREE, the LREE represent more enrichment.

Clay mineralogical record on the upper continental slope of the northwestern South China Sea since the Last Glacial Maximum

NASA Astrophysics Data System (ADS)

CHEN, Q.; Liu, Z.; Stattegger, K.

2012-12-01

Clay mineralogy of two gravity cores (18428 and 18429) on the upper continental slope of the northwestern South China Sea was investigated in order to understand terrigenous sediment sources and to evaluate the contribution from the Red River since the Late Glacial Maximum. Planktonic foraminiferal oxygen isotope and carbonate stratigraphies suggest that Core 18428 is constrained in Holocene while Core 18429 covers the period of MIS 1-2. Clay mineral assemblages of two cores are composed mainly of smectite (18-57%) and illite (21-41%), with minor chlorite (12-21%) and kaolinite (8-26%). In despite of relatively constant values of illite crystallinity, ranging among 0.14°-0.20° Δ2θ, the time series variation in clay mineral distributions indicates a strong glacial-interglacial shift. Contents of illite, chlorite, and kaolinite (Core 18429) in the Holocene are lower than in the glacial period, and vice versa for the smectite content. The provenance analysis based on clay mineralogy suggests the Red River as a predominant sedimentary source of illite, chlorite, and kaolinite during all the depositional period of MIS 1-2. The sea level change actually controlled the variations of clay mineral assemblages on the upper slope since the Last Glacial Maximum. When the sea level was low during the last glacial period, more terrigenous sediments from the Red River could reach the continental slope in the northwestern South China Sea. However, when the sea level is closed to the present situation during the Holocene, most of Red River sediments could be trapped in the Gulf of Tonkin, instead of draining in the deep South China Sea.

Identification of spectrally similar materials using the USGS Tetracorder algorithm: The calcite-epidote-chlorite problem

USGS Publications Warehouse

Dalton, J.B.; Bove, D.J.; Mladinich, C.S.; Rockwell, B.W.

2004-01-01

A scheme to discriminate and identify materials having overlapping spectral absorption features has been developed and tested based on the U.S. Geological Survey (USGS) Tetracorder system. The scheme has been applied to remotely sensed imaging spectroscopy data acquired by the Airborne Visible and Infrared Imaging Spectrometer (AVIRIS) instrument. This approach was used to identify the minerals calcite, epidote, and chlorite in the upper Animas River watershed, Colorado. The study was motivated by the need to characterize the distribution of calcite in the watershed and assess its acid-neutralizing potential with regard to acidic mine drainage. Identification of these three minerals is difficult because their diagnostic spectral features are all centered at 2.3 ??m, and have similar shapes and widths. Previous studies overestimated calcite abundance as a result of these spectral overlaps. The use of a reference library containing synthetic mixtures of the three minerals in varying proportions was found to simplify the task of identifying these minerals when used in conjunction with a rule-based expert system. Some inaccuracies in the mineral distribution maps remain, however, due to the influence of a fourth spectral component, sericite, which exhibits spectral absorption features at 2.2 and 2.4 ??m that overlap the 2.3-??m absorption features of the other three minerals. Whereas the endmember minerals calcite, epidote, chlorite, and sericite can be identified by the method presented here, discrepancies occur in areas where all four occur together as intimate mixtures. It is expected that future work will be able to reduce these discrepancies by including reference mixtures containing sericite. ?? 2004 Elsevier Inc. All rights reserved.

In-situ generation of chlorine dioxide for surface decontamination of produce

USDA-ARS?s Scientific Manuscript database

Fruits and vegetables, particularly fresh-cut products, are frequently contaminated with bacterial pathogens and implicated in foodborne illnesses. The objective of this study was to develop a unique in-situ sequential surface decontamination method for produce using sodium chlorite and acid. The ...

Multiple hydrothermal and metamorphic events in the Kidd Creek volcanogenic massive sulphide deposit, Timmins, Ontario: evidence from tourmalines and chlorites

USGS Publications Warehouse

Slack, J.F.; Coad, P.R.

1989-01-01

The tourmalines and chlorites record a series of multiple hydrothermal and metamorphic events. Paragenetic studies suggest that tourmaline was deposited during several discrete stages of mineralization, as evidence by brecciation and cross-cutting relationships. Most of the tourmalines have two concentric growth zones defined by different colours (green, brown, blue, yellow). Some tourmalines also display pale discordant rims that cross-cut and embay the inner growth zones and polycrystalline, multiple-extinction domains. Late sulphide veinlets (chalcopyrite, pyrrhotite) transect the inner growth zones and pale discordant rims of many crystals. The concentric growth zones are interpreted as primary features developed by the main ore-forming hydrothermal system, whereas the discordant rims, polycrystalline domains, and cross-cutting sulphide veinlets reflect post-ore metamorphic processes. Variations in mineral proportions and mineral chemistry within the deposit mainly depend on fluctuations in temperature, pH, water/rock ratios, and amounts of entrained seawater. -from Authors

Authigenic chlorite as a controlling factor in the exploration of Turonian/Coniacian turbidites in the Santos Basin

DOE Office of Scientific and Technical Information (OSTI.GOV)

Porsche, E.; Lopes de Freitas, E.

1996-08-01

Upper Turonian/Coniacian and Campanian turbidites are major targets for petroleum exploration in the Santos Basin, southeastern Brazil. They occur between 140 and 1000 m of present water depth, are buried at about 4500 m, and reach thickness of up to 60 m. The main reservoir facies is composed of unstratified, fine to very fine grained, poorly sorted sandstones, which framework is compositionally immature, including a high proportion of feldspars and volcanic rock fragments. Early coating of grains by authigenic chlorite inhibited pressure solution and quartz cementation in the reservoir. This diagenetic characteristic allowed important preservation of primary porosity (>20%) inmore » the reservoir; nevertheless its permeability never exceeds 30 ml. The study of sedimentary facies and related depositional processes has been conducted to predict the distribution of petroleum-bearing turbidites throughout the Santos Basin; this comprises a major challenge for the petroleum exploration in this important Brazilian exploration frontier.« less

Reverse osmosis membrane composition, structure and performance modification by bisulphite, iron(III), bromide and chlorite exposure.

PubMed

Ferrer, O; Gibert, O; Cortina, J L

2016-10-15

Reverse osmosis (RO) membrane exposure to bisulphite, chlorite, bromide and iron(III) was assessed in terms of membrane composition, structure and performance. Membrane composition was determined by Rutherford backscattering spectrometry (RBS) and membrane performance was assessed by water and chloride permeation, using a modified version of the solution-diffusion model. Iron(III) dosage in presence of bisulphite led to an autooxidation of the latter, probably generating free radicals which damaged the membrane. It comprised a significant raise in chloride passage (chloride permeation coefficient increased 5.3-5.1 fold compared to the virgin membrane under the conditions studied) rapidly. No major differences in terms of water permeability and membrane composition were observed. Nevertheless, an increase in the size of the network pores, and a raise in the fraction of aggregate pores of the polyamide (PA) layer were identified, but no amide bond cleavage was observed. These structural changes were therefore, in accordance with the transport properties observed. Copyright © 2016 Elsevier Ltd. All rights reserved.

Production of Dioxygen in the Dark: Dismutases of Oxyanions

PubMed Central

Ojha, Sunil

2016-01-01

O2 generating reactions are exceedingly rare in biology and difficult to mimic synthetically. Perchlorate-respiring bacteria enzymatically detoxify chlorite (ClO2−), the end product of the perchlorate (ClO4−) respiratory pathway, by rapidly converting it to dioxygen (O2) and chloride (Cl−). This reaction is catalyzed by a heme-containing protein, called chlorite dismutase (Cld), which bears no structural or sequence relationships with known peroxidases or other heme proteins and is part of a large family of proteins with more than one biochemical function. The original assumptions from the 1990s that perchlorate is not a natural product and that perchlorate respiration might be confined to a taxonomically narrow group of species have been called into question, as have the roles of perchlorate respiration and Cld-mediated reactions in the global biogeochemical cycle of chlorine. In this chapter, the chemistry and biochemistry of Cld-mediated O2 generation, as well as the biological and geochemical context of this extraordinary reaction, are described. PMID:25707466

The magnetic fabrics of experimentally deformed artificial clay-water dispersions

NASA Astrophysics Data System (ADS)

Richter, Carl; Frisch, Wolfgang; Ratschbacher, Lothar; Schwarz, Hans-Ulrich

1991-12-01

The development of magnetic fabrics in artificial clay-water dispersions and natural, hematite-bearing mudstones is investigated in plane-strain pure shear laboratory experiments under strain rates of 1.6 × 10 -5 and 2 × 10 -4s-1. The mixtures contain 0,15, 30 and 45% chlorite in an illite matrix, and 0, 1, 3, 6 and 8% magnetite in a kaolin matrix. Shortening up to 40% is imposed. The resulting fabrics show the following characteristics: (1) In the clay mixtures, the principal susceptibility axes ( kmax ≥ kint ≥ kmin) rotate away from the well defined initial fabric orientations into the princip strain directions ( e1 ≥ e2 ≥ e3) at strains > 30%. (2) Both mineralogical composition and initial magnetic fabric, but not the applied strain, influence the magnitudes of the principal susceptibility axes. (3) The illite-chlorite mixture series show an almost linear correlation between mineral concentration and susceptibility magnitudes. (4) Magnetite dominates the fabric of the magnetite-kaolin mixtures; the fabric is independent of the magnetite concentration.

Antiviral Activity of Chlorite-Oxidized Oxyamylose, a Polyacetal Carboxylic Acid

PubMed Central

Billiau, A.; Desmyter, J.; De Somer, P.

1970-01-01

Intraperitoneal injection of chlorite-oxidized oxyamylose (COAM) protected mice against mengo, vaccinia, Semliki Forest, and influenza APR8 viruses. Topical administration in the eye of rabbits partially inhibited the development of experimental herpetic keratoconjunctivitis. COAM resembled polyacrylic acid in many aspects, but it was markedly less toxic. For systemic administration, the therapeutic index was on the order of magnitude of 1:300 to 1:500. Although the in vivo antiviral effect of COAM wore off faster than that of polyacrylic acid, protection lasted for several weeks. Against mengovirus, such prolonged protection was achieved only when polymer and virus were injected intraperitoneally. Protection against intravenous vaccinia virus was not dependent on the injection route of COAM. Experiments on the mode of action of COAM pointed to macrophages as possible mediators of the antiviral effect. The fact that small amounts of interferon appeared in the serum after administration of high doses of COAM suggests that interferon may play a role in the induction of antiviral resistance by COAM. PMID:4314554

Continuum-based DFN-consistent numerical framework for the simulation of oxygen infiltration into fractured crystalline rocks

NASA Astrophysics Data System (ADS)

Trinchero, Paolo; Puigdomenech, Ignasi; Molinero, Jorge; Ebrahimi, Hedieh; Gylling, Björn; Svensson, Urban; Bosbach, Dirk; Deissmann, Guido

2017-05-01

We present an enhanced continuum-based approach for the modelling of groundwater flow coupled with reactive transport in crystalline fractured rocks. In the proposed formulation, flow, transport and geochemical parameters are represented onto a numerical grid using Discrete Fracture Network (DFN) derived parameters. The geochemical reactions are further constrained by field observations of mineral distribution. To illustrate how the approach can be used to include physical and geochemical complexities into reactive transport calculations, we have analysed the potential ingress of oxygenated glacial-meltwater in a heterogeneous fractured rock using the Forsmark site (Sweden) as an example. The results of high-performance reactive transport calculations show that, after a quick oxygen penetration, steady state conditions are attained where abiotic reactions (i.e. the dissolution of chlorite and the homogeneous oxidation of aqueous iron(II) ions) counterbalance advective oxygen fluxes. The results show that most of the chlorite becomes depleted in the highly conductive deformation zones where higher mineral surface areas are available for reactions.

Characterization of the Fault Core and Damage Zone of the Borrego Fault, 2010 M7.2 Rupture

NASA Astrophysics Data System (ADS)

Dorsey, M. T.; Rockwell, T. K.; Girty, G.; Ostermeijer, G.; Mitchell, T. M.; Fletcher, J. M.

2017-12-01

We collected a continuous sample of the fault core and 23 samples of the damage zone out to 52 m across the rupture trace of the 2010 M7.2 El Mayor-Cucapa earthquake to characterize the physical damage and chemical transformations associated with this active seismic source. In addition to quantifying fracture intensity from macroscopic analysis, we cut a continuous thin section through the fault core and from various samples in the damage zone, and ran each sample for XRD analyses for clay mineralogy, XRF for bulk geochemical analyses, and bulk and grain density from which porosity and volumetric strain were derived. The parent rock is a hydrothermally-altered biotite tonalite, with biotite partially altered to chlorite. The presence of epidote with chlorite suggests that these rocks were subjected to relatively high temperatures of 300-400° C. Adjacent to the outermost damage zone is a chaotic breccia zone with distinct chemical and physical characteristics, indicating possible connection to an ancestral fault to the southwest. The damage zone consists of an outer zone of protocataclasite, which grades inward towards mesocataclasite with seams of ultracataclasite. The fault core is anomalous in that it is largely composed of a sliver of marble that has been translated along the fault, so direct comparison with the damage zone is impaired. From collected data, we observe that chloritization increases into the breccia and damage zones, as does the presence of illite. Porosity reaches maximum values in the damage zone adjacent to the core, and closely follows trends in fracture intensity. Statistically significant gains in Mg, Na, K, Mn, and total bulk mass occurred within the inner damage zone, with losses of Ca and P mass, which led to the formation of chlorite and albite. The outer damage zone displays gains in Mg and Na mass with losses in Ca and P mass. The breccia zone shows gains in mass of Mg and Mn and loss in total bulk mass. A gain in LOI in both the breccia and damage zones is attributed to formation of clay. Volumetric strain tracks porosity, as expected, and increases towards the core. Notably, damage appears to be superposed on chemical alterations, which supports the idea that much of the hydrothermal alteration occurred at depth followed by brecciation and cataclasis once the fault zone rocks were exhumed closer to the surface.

Formation of A-type granites in the Lower Yangtze River Belt: A perspective from apatite geochemistry

NASA Astrophysics Data System (ADS)

Jiang, Xiao-Yan; Li, He; Ding, Xing; Wu, Kai; Guo, Jia; Liu, Ji-Qiang; Sun, Wei-Dong

2018-04-01

Apatite is ubiquitous in A-type granites, and can be used to elucidate the volatile contents of the silicate melt, which reflect its source characteristics. A-type granites have been recognized as a distinct group of granites. A1- and A2-type subgroups are produced under different extensional settings. However, the details of the mechanisms behind the distinctive geochemical characteristics of A1- and A2-type granites remain obscure. Belts of Cretaceous A1- and A2-type granites occur along the Lower Yangtze River Belt in eastern China. Here we investigated the major and trace element compositions of apatites from contemporary A1- and A2-type granites at different localities along the Lower Yangtze River Belt, in order to decipher their discrepant source processes. Apatites from A1- and A2-type granites show similar major and trace elements, but differ in their F and Cl concentrations. Apatites from A1-type granites in the eastern part of the Lower Yangtze River Belt have much lower F and higher Cl concentrations compared to A2-type granites in the western part. Moreover, from the east to the west, the F concentrations of apatites from A1-type granites increase, while the Cl concentrations decline. In a subducted plate, F is retained by amphibole, chlorite, serpentine and mica minerals through the amphibolite stage, and finally by phengite and lawsonite during the eclogite stage, whereas, Cl is controlled by amphibole, chlorite and serpentine. The high and varied Cl concentrations in A1 subgroup apatites, therefore, may be attributed to the breakdown of amphibole, chlorite and/or serpentine decomposition during partial melting of subducted oceanic crust releasing a large amount of Cl at shallower depth. In contrast, F is transported to deeper depths in the subducted oceanic crust, and released through breakdown of phengite and lawsonite, making an important contribution to the formation of A2-type granites. Apatites from A1- and A2-type granite samples show regular changes in LREE/HREE, LREE/MREE and MREE/HREE ratios with increasing distance from the location of the subduction zone, probably as the result of nonsynchronous dehydration of the serpentine and phengite at different stages during subduction. We propose that A1- and A2-type granites on the Lower Yangtze River Belt were derived from sources metasomatised by fluids originating from the breakdown of amphibole, chlorite and/or serpentine with higher Cl, lower F, and from phengite and/or lawsonite with relatively higher F but lower Cl, respectively.

Dissection of the mechanism of manganese porphyrin-catalyzed chlorine dioxide generation.

PubMed

Umile, Thomas P; Wang, Dong; Groves, John T

2011-10-17

Chlorine dioxide, an industrially important biocide and bleach, is produced rapidly and efficiently from chlorite ion in the presence of water-soluble, manganese porphyrins and porphyrazines at neutral pH under mild conditions. The electron-deficient manganese(III) tetra-(N,N-dimethyl)imidazolium porphyrin (MnTDMImP), tetra-(N,N-dimethyl)benzimidazolium (MnTDMBImP) porphyrin, and manganese(III) tetra-N-methyl-2,3-pyridinoporphyrazine (MnTM23PyPz) were found to be the most efficient catalysts for this process. The more typical manganese tetra-4-N-methylpyridiumporphyrin (Mn-4-TMPyP) was much less effective. Rates for the best catalysts were in the range of 0.24-32 TO/s with MnTM23PyPz being the fastest. The kinetics of reactions of the various ClO(x) species (e.g., chlorite ion, hypochlorous acid, and chlorine dioxide) with authentic oxomanganese(IV) and dioxomanganese(V)MnTDMImP intermediates were studied by stopped-flow spectroscopy. Rate-limiting oxidation of the manganese(III) catalyst by chlorite ion via oxygen atom transfer is proposed to afford a trans-dioxomanganese(V) intermediate. Both trans-dioxomanganese(V)TDMImP and oxoaqua-manganese(IV)TDMImP oxidize chlorite ion by 1-electron, generating the product chlorine dioxide with bimolecular rate constants of 6.30 × 10(3) M(-1) s(-1) and 3.13 × 10(3) M(-1) s(-1), respectively, at pH 6.8. Chlorine dioxide was able to oxidize manganese(III)TDMImP to oxomanganese(IV) at a similar rate, establishing a redox steady-state equilibrium under turnover conditions. Hypochlorous acid (HOCl) produced during turnover was found to rapidly and reversibly react with manganese(III)TDMImP to give dioxoMn(V)TDMImP and chloride ion. The measured equilibrium constant for this reaction (K(eq) = 2.2 at pH 5.1) afforded a value for the oxoMn(V)/Mn(III) redox couple under catalytic conditions (E' = 1.35 V vs NHE). In subsequent processes, chlorine dioxide reacts with both oxomanganese(V) and oxomanganese(IV)TDMImP to afford chlorate ion. Kinetic simulations of the proposed mechanism using experimentally measured rate constants were in agreement with observed chlorine dioxide growth and decay curves, measured chlorate yields, and the oxoMn(IV)/Mn(III) redox potential (1.03 V vs NHE). This acid-free catalysis could form the basis for a new process to make ClO(2).

Development of chlorine dioxide releasing film and its application in decontaminating fresh produce

USDA-ARS?s Scientific Manuscript database

A feasibility study was conducted to develop chlorine dioxide releasing packaging films for decontaminating fresh produce. Sodium chlorite and citric acid powder were incorporated into polylactic acid (PLA) polymer. Films made with different amount of PLA (100 & 300 mg), percentage of reactant (5-60...

Evaluation of gaseous chlorine dioxide for the inactivation of tulane virus on blueberries

USDA-ARS?s Scientific Manuscript database

To determine the effectiveness of gaseous chlorine dioxide against a human norovirus surrogate on produce, chlorine dioxide was generated and applied to Tulane virus coated blueberries in a 240 ml treatment chamber. Chlorine dioxide was produced by acidifying sodium chlorite solution. Initial asse...

Thermal inactivation of Salmonella Typhimurium on dressed chicken skin previously exposed to acidified sodium chlorite or carvacrol

USDA-ARS?s Scientific Manuscript database

Salmonella is a leading cause of foodborne illness, and live poultry is a main reservoir of this pathogen. Cross-contamination and transportation of contaminated poultry meat act as an important vehicle of Salmonella infections in humans. In this study, we assessed the effect of two antimicrobials:...

Ultrasound enhanced sanitizer efficacy in reduction of Escherichia coli O157:H7 population on spinach leaves

USDA-ARS?s Scientific Manuscript database

The use of ultrasound to enhance the efficacy of selected sanitizers in reduction of Escherichia coli O157:H7 populations on spinach was investigated. Spot-inoculated spinach samples were treated with water, chlorine, acidified sodium chlorite (ASC), peroxyacetic acid (POAA), and acidic electrolyzed...

Continuum-based DFN-consistent numerical framework for the simulation of oxygen infiltration into fractured crystalline rocks.

PubMed

Trinchero, Paolo; Puigdomenech, Ignasi; Molinero, Jorge; Ebrahimi, Hedieh; Gylling, Björn; Svensson, Urban; Bosbach, Dirk; Deissmann, Guido

2017-05-01

We present an enhanced continuum-based approach for the modelling of groundwater flow coupled with reactive transport in crystalline fractured rocks. In the proposed formulation, flow, transport and geochemical parameters are represented onto a numerical grid using Discrete Fracture Network (DFN) derived parameters. The geochemical reactions are further constrained by field observations of mineral distribution. To illustrate how the approach can be used to include physical and geochemical complexities into reactive transport calculations, we have analysed the potential ingress of oxygenated glacial-meltwater in a heterogeneous fractured rock using the Forsmark site (Sweden) as an example. The results of high-performance reactive transport calculations show that, after a quick oxygen penetration, steady state conditions are attained where abiotic reactions (i.e. the dissolution of chlorite and the homogeneous oxidation of aqueous iron(II) ions) counterbalance advective oxygen fluxes. The results show that most of the chlorite becomes depleted in the highly conductive deformation zones where higher mineral surface areas are available for reactions. Copyright © 2017 Elsevier B.V. All rights reserved.

Synergistic Effect of Sodium Chlorite and Edible Coating on Quality Maintenance of Minimally Processed Citrus grandis under Passive and Active MAP.

PubMed

Ban, Zhaojun; Feng, Jianhua; Wei, Wenwen; Yang, Xiangzheng; Li, Jilan; Guan, Junfeng; Li, Jiang

2015-08-01

Edible coating has been an innovation within the bioactive packaging concept. The comparative analysis upon the effect of edible coating, sodium chlorite (SC) and their combined application on quality maintenance of minimally processed pomelo (Citrus grandis) fruits during storage at 4 °C was conducted. Results showed that the combination of edible coating and SC dipping delayed the microbial development whereas the sole coating or dipping treatment was less efficient. The synergetic application of edible coating and SC treatment under modified atmosphere packaging (MAP, 10% O2 , 10% CO2 ) was able to maintain the total soluble solids level and ascorbic acid content, while reduce the weight loss as well as development of mesophiles and psychrotrophs. Nonetheless, the N, O-carboxymethyl chitosan solely coated samples showed significantly higher level of weight loss during storage with comparison to the untreated sample. Furthermore, the combined application of edible coating and SC dipping under active MAP best maintained the sensory quality of minimally processed pomelo fruit during storage. © 2015 Institute of Food Technologists®

Foliation boudinage

NASA Astrophysics Data System (ADS)

Arslan, Arzu; Passchier, Cees W.; Koehn, Daniel

2008-03-01

Foliation boudinage is a form of boudinage that develops in foliated rocks independent of lithology contrast. This paper describes foliation boudins from the Çine Massif in SW Turkey and the Furka Pass-Urseren Zone in central Switzerland. Four common types of foliation boudin structures can be distinguished in the field, named after vein geometries in their boudin necks in sections normal to the boudin axis: lozenge-, crescent-, X- and double crescent-type. The boudin necks are mostly filled with massive quartz in large single crystals, commonly associated with tourmaline, feldspar and biotite and in some cases with chlorite spherulites. The presence of blocky crystals and chlorite spherulites suggests that these veins formed as open, fluid-filled cavities during the initiation and development of foliation boudin structures, even in ductilely deforming gneiss at a depth of mid-crustal levels (7-10 kbar). The presence of cavities allowed the formation of closed fishmouth structures that are typical for many foliation boudins. The geometry of foliation boudin structures mainly depends on initial fracture orientation, propagation of the fracture during further deformation, and flow type in the wall rock.

Paleoproterozoic volcanic centers of the São Félix do Xingu region, Amazonian craton, Brazil: Hydrothermal alteration and metallogenetic potential

NASA Astrophysics Data System (ADS)

da Cruz, Raquel Souza; Fernandes, Carlos Marcello Dias; Villas, Raimundo Netuno Nobre; Juliani, Caetano; Monteiro, Lena Virgínia Soares; Lagler, Bruno; Misas, Carlos Mario Echeverri

2016-06-01

Geological, petrographic, scanning electron microscopy, and X-ray diffraction studies revealed hydrothermalized lithotypes evidenced by overprinted zones of potassic, propylitic, sericitic, and intermediate argillic alterations types, with pervasive and fracture-controlled styles, in Paleoproterozoic volcano-plutonic units of the São Félix do Xingu region, Amazonian craton, northern Brazil. The Sobreiro Formation presents propylitic (epidote + chlorite + carbonate + clinozoisite + sericite + quartz ± albite ± hematite ± pyrite), sericitic (sericite + quartz + carbonate), and potassic (potassic feldspar + hematite) alterations. The prehnite-pumpellyite pair that is common in geothermal fields also occurs in this unit. The Santa Rosa Formation shows mainly potassic (biotite + microcline ± magnetite), sericitic (sericite + quartz + carbonate ± chlorite ± gold), and intermediate argillic (montmorillonite + kaolinite/halloysite + illite) alterations. These findings strongly suggest the involvement of magma-sourced and meteoric fluids and draw attention to the metallogenetic potential of these volcanic units for Paleoproterozoic epithermal and rare and base metal porphyry-type mineralizations, similar to those already identified in other portions of the Amazonian craton.

Strength of the Subduction Plate Interface beneath the Seismogenic Zone: A Microstructural Investigation of Deformation Mechanisms within a Phyllosilicate- and Amphibole-rich Shear Zone

NASA Astrophysics Data System (ADS)

Seyler, C.; Kirkpatrick, J. D.; Šilerová, D.

2017-12-01

Localization of strain at plate boundaries requires rheological weakening of the lithosphere. The rheology of the subduction plate interface is dictated by the dominant grain-scale deformation mechanisms. However, little is known about the deformation mechanisms within phases commonly found in subduction zones, such as phyllosilicates and amphiboles. We investigate the Leech River Shear Zone on Vancouver Island, British Columbia to explore deformation processes downdip of the seismogenic zone and evaluate the bulk rheology of the plate interface. This shear zone juxtaposes a metamorphosed accretionary prism against a metabasaltic oceanic plateau, representing a paleo-plate interface from the ancient Cascadia subduction zone. Preliminary geothermometry results record a prograde deformation temperature of 573.6±11.2 ˚C in the overriding accretionary wedge, and the hornblende-chlorite-epidote-plagioclase mineral assemblage suggests upper greenschist to lower amphibolite facies metamorphism of the downgoing oceanic crust. Detailed mapping of the plate interface documents a 200 m wide mylonitic shear zone developed across the lithologic contact. Asymmetric shear fabrics, isoclinal folding, boudinage, and a steeply plunging, penetrative stretching lineation are consistent with sinistral-oblique subduction. Numerous discordant quartz veins are variably sheared into sigmoidal shapes as well as isoclinally folded and boudinaged, indicating cyclical synkinematic fracture and vein formation. At the grain-scale, interconnected, anastomosing layers of muscovite, chlorite, and graphite in the accretionary prism rocks likely deformed through kinking and dislocation glide. Framework minerals such as quartz and feldspar deformed by dislocation creep. In the metabasalt, hornblende and chlorite form a continuous S—C fabric in which asymmetric hornblende porphyroclasts deformed by rigid grain rotation and dissolution-precipitation creep. The strength of the subduction plate interface beneath the seismogenic zone was therefore controlled by multiple syn-kinematic mechanisms, with overall strength dominated by the rheology of phyllosilicates and amphibole, generating very low viscosities at the plate interface and enhancing strain localization.

Laramide alteration of proterozoic diabase: A likely contributor of copper to porphyry systems in the dripping spring mountains area, Southeastern Arizona

USGS Publications Warehouse

Force, E.R.

1998-01-01

Proterozoic diabase of the Dripping Spring range occurs as sills in the Proterozoic Apache Group and the Troy Quartzite and as intrusive sheets in basement rocks. The aggregate thickness of the diabase sills and intrusive sheets averages about 450 m in the part of the range showing little mid-Tertiary extension. Laramide alteration is of two types, dominated by chlorite and actinolite, respectively, and formed mostly from clinopyroxene. Actinolite-dominated assemblages are higher in Na and Ca. Hydrothermal biotite is common in the central areas of both alteration types. Laramide alteration forms two distribution patterns: a subequant pattern centered on Laramide intrusions and small porphyry deposits, characterized by actinolitic alteration, and a more extensive branching linear pattern that follows Laramide structures, centered on the larger Ray porphyry deposit, extending toward other Laramide districts and showing both alteration types. Alteration has apparently mobilized copper and other metals from diabase. The freshest diabase samples average about 120 ppm copper with little variation. In chloritic alteration, about 100 ppm of this copper is expelled in the most completely altered rocks. In actinolitic alteration, diabase may either gain or lose copper during alteration. Chloritic alteration constitutes roughly 70 percent of the diabase alteration in the study area, where alteration averages 41 percent complete. This implies liberation of about 9 ?? 106 tons (t) copper from diabase alteration, significantly less than the 16 ?? 106 t copper in Laramide mineral deposits of the superdistrict (Ray, Superior, Chilito, Christmas). However, diabase alteration may have been a significant component of the supply of copper to the Laramide mineral districts of the area. Synmineral magmatic sources of copper are not documented in this area. The distribution of Proterozoic diabase coincides with the central part of the southeastern Arizona copper province, which may thus owe much copper availability to an unusual abundance of diabase. However, many unanswered questions remain about metal supply from altering diabase.

Late Miocene to Pleistocene Mineralogy of ODP Site 1146

NASA Astrophysics Data System (ADS)

Arnold, E. M.

2001-12-01

ODP Site 1146 (19° 27.40'N, 116° 16.37'E, 2092 m depth) was drilled on the continental slope of the South China Sea. A composite section, comprised of three stratigraphic units, extends down to 640 mcd. Unit 1 is late Pliocene to Pleistocene nannofossil clay (0 - 243 mcd); Unit 2, middle Miocene to Late Pliocene foraminifera - nannofossil - clay mixed sediment (243 - 553 mcd); Unit 3, early to middle Miocene nannofossil clay (553 - 642 mcd). This study reports the < 2 μ m mineralogy from the late Miocene through early Pleistocene. Samples were analyzed at approximately 1.5 m intervals from 150 to 225 mcd, and 1 m intervals from 225 to 440 mcd, with an age resolution of ~25 ka and ~35 ka, respectively. Illite, chlorite, quartz and plagioclase concentrations decrease with increasing depth through Unit 1. Kaolinite and calcite concentrations increase with depth, while smectite values are constant in this unit. Illite, quartz and plagioclase show high variability in Unit 1 compared with the underlying Unit 2. Unit 2 has more uniform sediment composition, with constant illite, chlorite, and quartz concentrations. Kaolinite concentration increases with depth, following a drop in concentration across the Unit 1/2 boundary. Plagioclase concentration shows a small, steady decrease throughout this unit. Smectite concentration does not change across the Unit 1/2 boundary, decreases to a steady low value from 310 - 400 mcd, and increases again towards the bottom. The mineralogy of sediments recovered at Site 1146 suggest a classic pattern of source region aridification from the middle Pliocene through the Pleistocene, indicated in Unit 1 mineralogy as a decrease in kaolinite with decreasing depth, concomitant with an increase in quartz, plagioclase, illite and chlorite. The mineral variability in this interval suggests glacial - interglacial control of the terrigenous sedimentation. The sediment sources and source area weathering regimes were relatively constant throughout Unit 2, as indicated by low mineral variability and relatively constant mineral concentrations.

Mid Carboniferous lamprophyres, Cobequid Fault Zone, eastern Canada, linked to sodic granites, voluminous gabbro, and albitization

NASA Astrophysics Data System (ADS)

Pe-Piper, Georgia; Piper, David J. W.; Papoutsa, Angeliki

2018-01-01

Major intra-continental shear zones developed during the later stages of continental collision in a back-arc setting are sites of prolonged magmatism. Mantle metasomatism results from both melting of subducted sediments and oceanic crust. In the Cobequid Fault Zone of the northern Appalachians, back-arc A-type granites and gabbros dated ca. 360 Ma are locally intruded by lamprophyric dykes dated ca. 335 Ma. All the lamprophyres are kersantites with biotite and albite, lesser ilmenite, titanite and fluorapatite, and minor magmatic calcite, allanite, pyrite, magnetite, quartz and K-feldspar in some samples. The lamprophyres show enrichment in Rb, Ba, K, Th and REE and classify as calc-alkaline lamprophyre on the basis of biotite and whole rock chemistry. Pb isotopes lie on a mixing line between normal mantle-derived gabbro and OIB magma. Nd isotopes range from 1.3-3.5 εNdt, a little lower than in local gabbro. Most lamprophyres have δ18O = 3.8-4.4‰. Country rock is cut by pyrite-(Mg)-chlorite veins with euhedral allanite crystals that resemble the lamprophyres mineralogically, with the Mg-chlorite representing chloritized glass. Early Carboniferous unenriched mafic dykes and minor volcanic rocks are widespread along the major active strike-slip fault zones. The lamprophyres are geographically restricted to within 10 km of a small granitoid pluton with some sodic amphibole and widespread albitization. This was displaced by early Carboniferous strike-slip faulting from its original position close to the large Wentworth Pluton, the site of mantle-derived sodic amphibole granite, a major late gabbro pluton, and a volcanic carapace several kilometres thick, previously demonstrated to be the site of mantle upwelling and metasomatism. The age of the lamprophyres implies that enriched source material in upper lithospheric mantle or lower crust was displaced 50 km by crustal scale strike-slip faulting after enrichment by the mantle upwelling before lamprophyre emplacement. This indicates a multi-stage process to emplace lamprophyric magma.

Textural and chemical evolution of pyroxene during hydration and deformation: A consequence of retrograde metamorphism

NASA Astrophysics Data System (ADS)

Centrella, Stephen; Putnis, Andrew; Lanari, Pierre; Austrheim, Håkon

2018-01-01

Centimetre-sized grains of Al-rich clinopyroxene within the granulitic anorthosites of the Bergen Arcs, W-Norway undergo deformation by faults and micro-shear zones (kinks) along which fluid has been introduced. The clinopyroxene (11 wt% Al2O3) reacts to the deformation and hydration in two different ways: reaction to garnet (Alm41Prp32Grs21) plus a less aluminous pyroxene (3 wt% Al2O3) along kinks and the replacement of the Al-rich clinopyroxene by chlorite along cleavage planes. These reactions only take place in the hydrated part of a hand specimen that is separated from dry, unreacted granulite by a sharp interface that defines the limit of hydration. We use electron probe microanalysis (EPMA) and X-Ray mapping together with electron backscatter diffraction (EBSD) mapping to investigate the spatial and possible temporal relationships between these two parageneses. Gresens' analysis (Gresens, 1967) has been used to determine the mass balance and the local volume changes associated with the two reactions. The reaction to garnet + low-Al clinopyroxene induces a loss in volume of the solid phases whereas the chlorite formation gains volume. Strain variations result in local variation in undulose extinction in the parent clinopyroxene. EBSD results suggest that the density-increasing reaction to garnet + low-Al clinopyroxene takes place where the strain is highest whereas the density-decreasing reaction to chlorite forms away from shear zones where EBSD shows no significant strain. Modelling of phase equilibria suggest that the thermodynamic pressure of the assemblage within the shear zones is > 6 kbar higher than the pressure conditions for the whole rock for the same range of temperature ( 650 °C). This result suggests that the stress redistribution within a rock may play a role in determining the reactions that take place during retrograde metamorphism.

Clay-mineral suites, sources, and inferred dispersal routes: Southern California continental shelf

USGS Publications Warehouse

Hein, J.R.; Dowling, J.S.; Schuetze, A.; Lee, H.J.

2003-01-01

Clay mineralogy is useful in determining the distribution, sources, and dispersal routes of fine-grained sediments. In addition, clay minerals, especially smectite, may control the degree to which contaminants are adsorbed by the sediment. We analyzed 250 shelf sediment samples, 24 river-suspended-sediment samples, and 12 river-bed samples for clay-mineral contents in the Southern California Borderland from Point Conception to the Mexico border. In addition, six samples were analyzed from the Palos Verdes Headland in order to characterize the clay minerals contributed to the offshore from that point source. The <2 ??m-size fraction was isolated, Mg-saturated, and glycolated before analysis by X-ray diffraction. Semi-quantitative percentages of smectite, illite, and kaolinite plus chlorite were calculated using peak areas and standard weighting factors. Most fine-grained sediment is supplied to the shelf by rivers during major winter storms, especially during El Nin??o years. The largest sediment fluxes to the region are from the Santa Ynez and Santa Clara Rivers, which drain the Transverse Ranges. The mean clay-mineral suite for the entire shelf sediment data set (26% smectite, 50% illite, 24% kaolinite+chlorite) is closely comparable to that for the mean of all the rivers (31% smectite, 49% illite, 20% kaolinite+chlorite), indicating that the main source of shelf fine-grained sediments is the adjacent rivers. However, regional variations do exist and the shelf is divided into four provinces with characteristic clay-mineral suites. The means of the clay-mineral suites of the two southernmost provinces are within analytical error of the mineral suites of adjacent rivers. The next province to the north includes Santa Monica Bay and has a suite of clay minerals derived from mixing of fine-grained sediments from several sources, both from the north and south. The northernmost province clay-mineral suite matches moderately well that of the adjacent rivers, but does indicate some mixing from sources in adjacent provinces.

Metamorphic P-T evolution of the Gotsu blueschists from the Suo metamorphic belt in SW Japan: Implications for tectonic correlation with the Heilongjiang Complex, NE China

NASA Astrophysics Data System (ADS)

Kabir, Md. Fazle; Takasu, Akira; Li, Weimin

2018-05-01

In the Gotsu area of the c. 200 Ma high-P/T Suo metamorphic belt in the Inner Zone of southwest Japan, blueschists occur as lenses or layers within pelitic schists. Prograde, peak, and retrograde stages are distinguished in the blueschists, and the prograde and the peak metamorphic conditions are determined using pseudosection modelling in the NCKFMASHO system. The prograde metamorphic stage is defined by inclusions in porphyroblastic epidote and glaucophane, such as phengite, chlorite, albite, epidote and glaucophane/winchite, and the estimated metamorphic conditions are <325 °C and < 4-5 kbar at the boundary between the glaucophane schist facies and the greenschist facies. The peak metamorphic stage is well-defined by the schistosity-forming minerals, i.e. epidote, glaucophanic amphibole, phengite, and chlorite, suggesting the glaucophane schist facies conditions of 475-500 °C and 14-16 kbar. Actinolite/magnesiohornblende, chlorite, and albite replacing the peak stage minerals suggest the retrograde metamorphism into the greenschist facies. The metamorphic facies series of the Suo belt is defined by pumpellyite-actinolite facies to epidote-blueschist facies, and it has a relatively lower-P/T compared with the c. 300 Ma Renge belt in the Inner Zone of southwest Japan, which is defined by a sequence of lawsonite-blueschist facies to glaucophane-eclogite facies. The P- {M}_{{H}_2O} pseudosection and water isopleth show that the rocks were dehydrated during the initial stage of the exhumation and remained in water-saturated conditions. Similarities of the detrital zircon and peak metamorphic ages of the blueschists from the Suo metamorphic belt in southwest Japan and the Heilongjiang Complex in northeast China suggest that both metamorphic belts were probably formed in the same Paleo-Pacific subduction system in the Late Triassic to Jurassic period.

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

USGS Publications Warehouse

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 were acquired over 1 Ma. Compositional differences between soil and Zone C are largely attributed to illuvial processes, formation of additional Fe(III) oxides and incorporation of modern organic matter.

Mineral types of hydrothermal alteration zones in the Dukat ore field and their relationships to leucogranite and epithermal gold-silver ore, northeastern Russia

NASA Astrophysics Data System (ADS)

Filimonova, L. G.; Trubkin, N. V.; Chugaev, A. V.

2014-05-01

The paper considers the localization of potassic and propylitic hydrothermal alteration zones in the domal volcanic-plutonic structure controlling the position of the Dukat ore field with the eponymous unique epithermal Au-Ag deposit. Comprehensive mineralogical and geochemical data on rocks and minerals in hydrothermal alteration zones and associated intrusions have shown that quartz-jarosite-sericite, quartz-pyrite-sericite, and quartz-adularia-chlorite alterations were formed with the participation of fluid flows related to a fingerlike projection of a high-K leucogranite porphyry intrusion with large phenocrysts. These hydrothermal alterations developed in the rifted graben under conditions of divergent plate boundaries, whereas quartz-clinozoisite-calcite, epidote-chlorite, and garnet-calcite-chlorite alterations were linked to K-Na leucogranite intrusive bodies and developed under conditions of convergent plate boundaries reactivated as a result of formation of the marginal Okhotsk-Chukotka volcanic belt. Phase separation and coagulation of specific portions of ascending fluids resulted in the formation and stabilization of small-sized particles of native silver and other ore components, which enabled involvement in flows of secondary geothermal solutions and ore-forming fluids. The Sr, Nd, and Pb isotopic compositions of rocks and minerals from the hydrothermal alteration zones, associated intrusions, and economic orebodies at the Dukat deposit indicate that their components have been derived from the juvenile continental crust, which was altered in pre-Cretaceous periods of endogenic activity. The components of gangue minerals of potassic and propylitic hydrothertmal alterations and associated intrusions have been taken from deep sources differing in 87Sr/86Sr and 143Nd/144Nd at similar U/Pb and Th/Pb ratios. Chalcophile lead in products of hydrothermal activity and melanocratic inclusions in leucogranite has been taken from regions with elevated U/Pb and Th/Pb ratios.

Distribution of clay minerals on the Alaskan margin near Barrow Canyon revealed by Diffuse Spectral Reflectance measurements

NASA Astrophysics Data System (ADS)

Orsburn, C.; Ortiz, J. D.; Polyak, L.; Grebmeier, J. M.; Darby, D.

2007-12-01

Sediment clay mineral assemblages provide an excellent means of assessing the provenance of Arctic sediment due to the variety of sediment transport mechanisms at work and the existence of distinct weathering sources from differing bedrock geology. During HOTRAX Leg 1 aboard the USCG Ice breaker Healy (cruise HLY0501), we collected jumbo piston cores on the Alaskan margin near Barrow Canyon which provide detailed Holocene sedimentary records. Measurements of Diffuse Spectral Reflectance (DSR) were collected at 1cm resolution from the split surface of the cores using a Minolta CM-2600d UV/VIS spectrophotometer (400-700nm wavelength range; 10nm resolution; 3mm spot size). To interpret the resulting downcore records, we present a preliminary study using 28 coretop sediment samples collected by the Shelf-Basin Interaction program in 2004 arrayed in four transects across the shelf near Barrow Canyon. The samples were analyzed using an ASD Labspec Pro FR UV/VIS/NIR spectrometer (250-2500nm wavelength range, 2-10nm resolution; 20mm spot size). Our results indicate that the measurements from the two instruments are offset by constant factors, but can be easily compared. To estimate the clay mineralogy of the cores, we decomposed the matrix of DSR measurements from the coretop and downcore samples using principle component analysis and compared the resulting factor score patterns with mineral diffuse spectral reflectance signatures from known samples measured in our lab or available from version 5 of the USGS Digital Spectral Library. The three leading modes extracted by principle component analysis of the downcore samples are applicable to the coretops. We infer that the first principle component mode relates to smectite, the second to chlorite, and the third to a mixture of illite and goethite (herein referred to as illite - goethite). The geographic and bathymetric trends in the coretop data indicate that (1) the smectite and illite - goethite components both increase with depth and reach greater values in the two western transects than in the two eastern transects closest to the coast and Barrow Canyon, (2) the smectite and illite- goethite components are anticorrelated in the two western transects, but not in the two eastern transects, (3) chlorite decreases with depth and is highest in the two transects closest to Barrow Canyon. These results suggest that the chlorite on the Alaskan margin is transported by nearshore currents from the Bering Straight and then by bottom currents flowing through the Barrow Canyon. Accordingly, we interpret downcore chlorite peaks inferred from DSR measurements in our sediment cores as evidence of times of enhanced input of Pacific water to the Alaskan Margin.

Paragenesis and chemistry of multistage tourmaline formation in the sullivan Pb-Zn-Ag deposit, British Columbia

USGS Publications Warehouse

Jiang, S.-Y.; Palmer, M.R.; Slack, J.F.; Shaw, D.R.

1998-01-01

Detailed petrographic study, scanning electron microscope imaging, and electron microprobe analyses of tourmalines from the Sullivan Pb-Zn-Ag massive sulfide deposit (British Columbia, Canada) document multiple paragenetic stages and large compositional variations. The tourmalines mainly belong to two common solid-solution series: dravite-schorl and dravite-uvite. Ca- and Fe-rich feruvite and alkali-deficient tourmalines are present locally. Products of tourmaline-forming stages include (from oldest to youngest): (1) rare Fe-rich dravite-schorl within black tourmalinite clasts in footwall fragmental rocks; (2) widespread Mg-rich, very fine grained, felted dravite in the footwall (the main type of tourmaline in the footwall tourmalinite pipe); (3) recrystallized, Fe-rich dravite-schorl (locally Ca-Fe feruvite) in the tourmalinite pipe, which preferentially occurs near postore gabbroic intrusions; (4) Mg-rich dravite or uvite associated with chlorite-pyrrhotite and chlorite-albite-pyrite-altered rocks in the shallow footwall and hanging wall; (5) discrete Mg-rich tourmaline grains associated with chlorite and discordant Mg-rich tourmaline rims which occur on disseminated Fe-rich schorl in the bedded Pb-Zn-Ag ores. The timing of rare Fe-rich schorl in the bedded ores is uncertain, but it most likely occurred during or between stages 2 and 3. The different paragenetic stages and their respective tourmaline compositions are interpreted in terms of a multistage evolution involving contributions from: (1) variable mixtures of synsedimentary, Fe-rich hydrothermal fluids and entrained seawater; (2) postore, Fe-rich, gabbro-related hydrothermal fluids; and (3) postore metamorphic reactions. Early synsedimentary, Fe-rich hydrothermal fluids which contained little or no entrained seawater formed Fe-rich black tourmalinite clasts locally in the footwall. The major type of tourmaline in the footwall tourmalinite pipe is Mg rich, recording seawater entrainment under high water/rock conditions, rather than control by the chemical composition of the original host sediments. Rare Fe-rich schorl within the bedded Pb-Zn-Ag ores is believed to have formed on the sea floor by reaction of an Fe-rich brine pool with detrital aluminous sediments. Postore emplacement of gabbro sills and local dikes in the footwall produced Fe-rich hydrothermal fluids, which were responsible for formation of minor Fe-rich dravite-schorl which overprinted earlier dravite. Postore, but synsedimentary, hydrothermal alteration involving entrained seawater was responsible for deposition of dravite and uvite in the hanging wall and for dravite in the brown tourmalinites of the shallow footwall. Mg-rich dravite-uvite associated with chlorite and in discordant rims on schorl in the bedded ores formed by sulfide-silicate reactions during greenschist facies regional metamorphism.

Use of chemical sanitizers to reduce microbial populations and maintain quality of whole and fresh-cut cantaloupe

USDA-ARS?s Scientific Manuscript database

Whole cantaloupes either not inoculated or inoculated with Salmonella Poona were submerged in water, 100 ppm chlorine, acidified calcium sulfate (ACS: 1.2% Safe2O ACS50), 1000 ppm acidified sodium chlorite (Sanova), 80 ppm peroxyacetic acid (Tsunami), and combination of ACS and Tsunami for 10 min. ...

The heat capacities of osumilite from 298.15 to 1000 K, the thermodynamic properties of two natural chlorites to 500 K, and the thermodynamic properties of petalite to 1800 K.

USGS Publications Warehouse

Hemingway, B.S.; Robie, R.A.; Kittrick, J.A.; Grew, E.S.; Nelen, J.A.; London, D.

1984-01-01

Modifications to an automated low-T, adiabatic calorimeter are described. Thermodynamic data obtained with this instrument are reported for minerals from metamorphic terrains. (U.S. Bureau of Mines Report of Investigations 8451)-J.A.Z.

Weathering characteristics of wood plastic composites reinforced with extracted or delignified wood flour

Treesearch

Yao Chen; Nicole M. Stark; Mandla A. Tshabalala; Jianmin Gao; Yongming Fan

2016-01-01

This study investigated weathering performance of an HDPE wood plastic composite reinforced with extracted or delignified wood flour (WF). The wood flour was pre-extracted with three different solvents, toluene/ethanol (TE), acetone/water (AW), and hot water (HW), or sodium chlorite/acetic acid. The spectral properties of the composites before and after artificial...

Decay resistance of wood-plastic composites reinforced with extracted or delignified wood flour

Treesearch

Rebecca E. Ibach; Yao Chen; Nicole M. Stark; Mandla A. Tshabalala; Yongming Fan; Jianmin Gao

2014-01-01

The moisture and decay resistance of wood-plastic composites (WPCs) reinforced with extracted or delignified wood flour (WF) was investigated. Three different extractions were preformed: toluene/ethanol (TE), acetone/water (AW), and hot water (HW). Delignification (DL) was performed using a sodium chlorite/acetic acid solution. All WPCs specimens were made with 50% by...

21 CFR 173.325 - Acidified sodium chlorite solutions.

Code of Federal Regulations, 2012 CFR

2012-04-01

... a prechiller or chiller tank; (ii) In a prechiller or chiller solution for application to the intact... a prechiller or chiller solution for application to poultry carcass parts; or (v) As a component of... a level sufficient to achieve a solution pH of 2.3 to 2.9. (3) When used in a prechiller or chiller...

Moisture Performance of wood-plastic composites reinforced with extracted and delignified wood flour

Treesearch

Yao Chen; Nicole M. Stark; Mandla A. Tshabalala; Jianmin Gao; Yongming Fan

2014-01-01

This study investigated the effect of using extracted and delignified wood flour on water sorption properties of wood–plastic composites. Wood flour (WF) extraction was performed with three solvent systems: toluene/ethanol (TE), acetone/water (AW), and hot water (HW); delignification was conducted using sodium chlorite/acetic acid solution. A 24 full-factorial...

Properties of wood-plastic composites (WPCs) reinforced with extracted and delignified wood flour

Treesearch

Yao Chen; Nicole M. Stark; Mandla A. Tshabalala; Jianmin Gao; Yongming Fan

2014-01-01

The water sorption and mechanical properties of wood-plastic composites (WPCs) made of extracted and delignified wood flour (WF) has been investigated. WF was prepared by extraction with the solvent systems toluene/ethanol (TE), acetone/water (AW), and hot water (HW), and its delignification was conducted by means of sodium chlorite/acetic acid (AA) solution. A 2 4...

Revealing organization of cellulose in wood cell walls by Raman imaging

Treesearch

Umesh P. Agarwal; Sally A. Ralph

2007-01-01

Anisotropy of cellulose organization in mature black spruce wood cell wall was investigated by Raman imaging using a 1 [mu]m lateral-resolution capable confocal Raman microscope. In these studies, wood cross sections (CS) and radial longitudinal sections (LS) that were partially delignified by acid chlorite treatment were used. In the case of CS where latewood cells...

Disinfecting capabilities of oxychlorine compounds.

PubMed Central

Noss, C I; Olivieri, V P

1985-01-01

The bacterial virus f2 was inactivated by chlorine dioxide at acidic, neutral, and alkaline pH values. The rate of inactivation increased with increasing pH. Chlorine dioxide disproportionation products, chlorite and chlorate, were not active disinfectants. As chlorine dioxide solutions were degraded under alkaline conditions, they displayed reduced viricidal effectiveness, thereby confirming the chlorine dioxide free radical as the active disinfecting species. PMID:3911893

Mid-Holocene Strengthening of the Bering Strait Inflow to the Arctic and its Linkage With the North Atlantic Subpolar Gyre Circulation

NASA Astrophysics Data System (ADS)

Yamamoto, M.; Nam, S. I.; Polyak, L.; Kobayashi, D.; Suzuki, K.; Irino, T.; Shimada, K.

2017-12-01

The Bering Strait inflow (BSI) is an important element of the Arctic Ocean circulation system. We report records of the chlorite/illite ratios in three sediment cores from the northern Chukchi Sea providing insights into the long-term dynamics of the BSI during the Holocene. The BSI approximation by the chlorite/illite record, despite a considerable geographic variability, consistently shows intensified flow from the Bering Sea to the Arctic during the middle Holocene, which is attributed primarily to the effect of higher atmospheric pressure over the Aleutian Basin. The intensified BSI was associated with decrease in sea-ice concentrations and increase in marine production, as indicated by biomarker concentrations, suggesting a major influence of the BSI on sea-ice and biological conditions in the Chukchi Sea. Multi-century to millennial fluctuations, presumably controlled by solar activity, were also identified. This middle Holocene strengthening of the BSI was coeval with intense subpolar gyre circulation in the North Atlantic. We propose that the BSI is linked with the North Atlantic circulation via an atmospheric teleconnection between the Aleutian and Icelandic Lows.

The Nature of Hololignin

DOE Office of Scientific and Technical Information (OSTI.GOV)

Meng, Xianzhi; Pu, Yunqiao; Sannigrahi, Poulomi

Acid chlorite delignification is frequently used to obtain a mixture of cellulose and hemicellulose known as holocellulose from biomass. While a majority of lignin is removed after holocellulose pulping, there appears to be a minor fraction of lignin that is more resistant to acid chlorite treatment and remains in the holocellulose even after repeated delignification treatment. This type of lignin, defined as hololignin, has not been characterized, is likely to contribute to biomass recalcitrance and is clearly of fundamental interest to understand its structural characteristics. In this study, hololignin isolated from poplar holocellulose was characterized with a wide array ofmore » techniques including GPC, quantitative 13C, DEPT-135, HSQC, and 31P NMR. The results were then compared to those from milled wood lignin (MWL), the representative native lignin isolated from poplar. NMR analysis demonstrated a depletion of cinnamyl aldehyde, acetyl group, and decrease of p-hydroxybenzoate structural units in hololignin. An enrichment of condensed structures in hololignin was observed. Hololignin also had a significantly lower molecular weight than MWL. Finally, hololignin is relatively enriched in guaiacyl units and has a lower S/G ratio, lower β-O-4 ether linkages, fewer aliphatic and phenolic hydroxyl groups, and more carboxylic acid groups than MWL.« less

Slip localization on the southern Alpine Fault, New Zealand

NASA Astrophysics Data System (ADS)

Barth, N. C.; Boulton, C.; Carpenter, B. M.; Batt, G. E.; Toy, V. G.

2013-06-01

of a detailed field study of the southern onshore portion of New Zealand's Alpine Fault reveal that for 75 km along-strike, dextral-normal slip on this long-lived structure is highly localized in phyllosilicate-rich fault core gouges and along their contact with more competent rocks. At three localities (Martyr River, McKenzie Creek, and Hokuri Creek), we document complete cross sections through the fault. New 40Ar/39Ar dates on mylonites, combined with microstructural and mechanical data on phyllosilicate-rich fault core gouges show that modern slip is localized onto a single, steeply dipping 1 to 12 m-thick fault core composed of impermeable (k = 10-20 to 10-22 m2), frictionally weak (μs = 0.12-0.37), velocity-strengthening, illite-chlorite, and saponite-chlorite-lizardite fault gouges. Fault core materials are (1) comparable to those of other major weak-cored faults (e.g., San Andreas Fault) and (2) most compatible with fault creep, despite paleoseismic evidence of quasiperiodic large magnitude earthquakes (Mw > 7) on this portion of the Alpine Fault. We conclude that frictional properties of gouges at the surface do not characterize the overall seismogenic behavior of the southern Alpine Fault.

The Nature of Hololignin

DOE PAGES

Meng, Xianzhi; Pu, Yunqiao; Sannigrahi, Poulomi; ...

2017-11-07

Acid chlorite delignification is frequently used to obtain a mixture of cellulose and hemicellulose known as holocellulose from biomass. While a majority of lignin is removed after holocellulose pulping, there appears to be a minor fraction of lignin that is more resistant to acid chlorite treatment and remains in the holocellulose even after repeated delignification treatment. This type of lignin, defined as hololignin, has not been characterized, is likely to contribute to biomass recalcitrance and is clearly of fundamental interest to understand its structural characteristics. In this study, hololignin isolated from poplar holocellulose was characterized with a wide array ofmore » techniques including GPC, quantitative 13C, DEPT-135, HSQC, and 31P NMR. The results were then compared to those from milled wood lignin (MWL), the representative native lignin isolated from poplar. NMR analysis demonstrated a depletion of cinnamyl aldehyde, acetyl group, and decrease of p-hydroxybenzoate structural units in hololignin. An enrichment of condensed structures in hololignin was observed. Hololignin also had a significantly lower molecular weight than MWL. Finally, hololignin is relatively enriched in guaiacyl units and has a lower S/G ratio, lower β-O-4 ether linkages, fewer aliphatic and phenolic hydroxyl groups, and more carboxylic acid groups than MWL.« less

Efficacy of Sodium Hypochlorite and Acidified Sodium Chlorite in Preventing Browning and Microbial Growth on Fresh-Cut Produce

PubMed Central

Sun, Shih Hui; Kim, Su Jin; Kwak, Soo Jin; Yoon, Ki Sun

2012-01-01

The use of suitable sanitizers can increase the quality of fresh-cut produce and reduce the risk of foodborne illnesses. The objective of this study was to compare the washing effects of 100 mg/L sodium hypochlorite (SH) and 500 mg/L acidified sodium chlorite (ASC) on the prevention of enzymatic browning and the growth of microbial populations, including aerobic plate counts, E. coli, and coliforms, throughout storage at 4°C and 10°C. Fresh-cut zucchini, cucumbers, green bell peppers, and root vegetables such as potatoes, sweet potatoes, carrots, and radishes were used. Compared to SH washing, ASC washing significantly (p<0.05) reduced microbial contamination on the fresh-cut produce and prevented browning of fresh-cut potatoes and sweet potatoes during storage. More effective inhibition of aerobic plate counts and coliforms growth was observed on fresh-cut produce treated with ASC during storage at 10°C. Polyphenol oxidase (PPO) activity of fresh-cut potatoes and sweet potatoes was more effectively inhibited after washing with ASC. The use of 500 mg/L ASC can provide effective antimicrobial and anti-browning treatments of fresh-cut produce, including processed root vegetables. PMID:24471086

Efficacy of sodium hypochlorite and acidified sodium chlorite in preventing browning and microbial growth on fresh-cut produce.

PubMed

Sun, Shih Hui; Kim, Su Jin; Kwak, Soo Jin; Yoon, Ki Sun

2012-09-01

The use of suitable sanitizers can increase the quality of fresh-cut produce and reduce the risk of foodborne illnesses. The objective of this study was to compare the washing effects of 100 mg/L sodium hypochlorite (SH) and 500 mg/L acidified sodium chlorite (ASC) on the prevention of enzymatic browning and the growth of microbial populations, including aerobic plate counts, E. coli, and coliforms, throughout storage at 4°C and 10°C. Fresh-cut zucchini, cucumbers, green bell peppers, and root vegetables such as potatoes, sweet potatoes, carrots, and radishes were used. Compared to SH washing, ASC washing significantly (p<0.05) reduced microbial contamination on the fresh-cut produce and prevented browning of fresh-cut potatoes and sweet potatoes during storage. More effective inhibition of aerobic plate counts and coliforms growth was observed on fresh-cut produce treated with ASC during storage at 10°C. Polyphenol oxidase (PPO) activity of fresh-cut potatoes and sweet potatoes was more effectively inhibited after washing with ASC. The use of 500 mg/L ASC can provide effective antimicrobial and anti-browning treatments of fresh-cut produce, including processed root vegetables.

Rodingitization and hydration of the oceanic lithosphere as developed in the Leka ophiolite, north central Norway

NASA Astrophysics Data System (ADS)

Austrheim, H.; Prestvik, T.

2008-08-01

Ophiolite complexes in mountain chains may give supplementary information on the hydration of the oceanic lithosphere to that obtained from dredged and drilled samples from the ocean floor. The ultramafic (mantle) and the layered ultramafic to anorthositic (crustal) sequences of the Cambrian (497 Ma) Leka ophiolite are variably serpentinized and chloritized. Grossular-rodingite (rodingite s.s.) has been found over a c.500 m long and tens of meters wide zone in the layered, crustal section of the complex and is developed in both pyroxenites and gabbro/anorthosite layers. Shear zones and meter wide fracture zones, where the rock has developed a fracture cleavage, are oriented at high angel to the layering and these zones were the main conduits for transport of fluid and solute between the various lithologies. Some 5-15 cm thick layers of anorthosite (or leucogabbro) have been rodingitized around such a fractures zone, with the development of three distinct metasomatic zones along the plagioclase layer. A central grossular-dominated zone with clinopyroxene, clinozoisite, prehnite, chlorite and minor titanite (rodingite zone) extends for up to 3 m along strike and gives way to a clinozoisite-dominated zone (typically 0.5 m wide) with additional grossular, clinopyroxene and chlorite which is followed outward by a LILE-enriched zone (LILE-zone) with clinozoisite, phlogopite, K-feldspar, plagioclase and preiswerkite. The LILE-zone extends more than 3 m out from the clinozoisite-dominated zone (Clz-zone). Assuming constant volume, the rodingite formed from the plagioclase layer by addition of 20 g of CaO per 100 g of rock. All Na 2O (c. 2 g) was removed from both rodingite- and Clz-zones. Ti and V increase almost 10× in the rodingite compared to its protolith. K, Ba, Rb and Cs are strongly enriched in the LILE-zone compared to the protolith and suggest interaction with sea water. The lithologies alternating with the plagioclase layers (clinopyroxenite, wehrlite, websterite and dunite) display textures indicating a number of Ca-releasing (Cpx → Chl, Cpx → Srp, Cpx → Amph) and Ca-consuming (Opx → Cpx2, Ol → Cpx2, Cpx1 → Cpx2) reactions. The replacement textures are distributed around fracture and shear zones, with the Ca -releasing reactions in the core and the Ca -consuming reactions in distal parts, forming a metasomatic column out from the fluid pathways. Serpentinization and chloritization of clinopyroxene was the main Ca-source for the rodingitization process. This first description of rodingite in a layered sequence of an ophiolite complex indicates that the hydration of the oceanic lithosphere occurred at various structural levels and was associated with Ca-metasomatism also in places where rodingite s.s. is lacking. The different lithologies exchanged elements through transport on shear and fracture zones.

Viability of Listeria monocytogenes on uncured turkey breast commercially-prepared with and without buffered vinegar during extended storage at 4 degrees and 10 degrees C

USDA-ARS?s Scientific Manuscript database

We determined the viability of Listeria monocytogenes on uncured turkey breast containing buffered vinegar (BV) and surface treated with a stabilized solution of sodium chlorite in vinegar (VSC). Commercially-produced, uncured, deli-style turkey breast was formulated with BV (0.0, 2.0, 2.5, or 3.0%)...

Color and Surface Chemistry Changes of Pine Wood Flour after Extraction and Delignification

Treesearch

Yao Chen; Mandla A. Tshabalala; Jianmin Gao; Nicole M. Stark; Yongming Fan

2014-01-01

A detailed study was undertaken to examine the color and chemistry changes of pine wood flour when its extractives are removed and when it is delignified. The solvent systems employed were toluene/ethanol (TE), acetone/water (AW), and hot-water (HW), while sodium chlorite/acetic acid were used for delignification (i.e., lignin removal (LR)). Samples were analyzed by...

Mössbauer study of Brazilian soapstone

NASA Astrophysics Data System (ADS)

Gonçalves, M. A.; de Jesus Filho, M. F.; Garg, V. K.

1991-11-01

Steatite mineral rocks, soapstone, have been studied by X-ray diffraction, optical microscopic analysis (modal analysis), electron probe micro analysis and Mössbauer spectroscopy for characterization, mineral percentages and chemical composition. Mössbauer spectra show both, magnetic interactions corresponding to magnetite and doublets corresponding to talc. chlorite, dolomite and tremolite. The temperature dependence of the quadrupole splitting in dolomite has been explained in terms of crystal field interaction.

Oceanic Lithosphere Magnetization: Marine Magnetic Investigations of Crustal Accretion and Tectonic Processes in Mid-Ocean Ridge Environments

DTIC Science & Technology

2007-09-01

vs TiO2 ...................... . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 238 A2.4 Discussion...types can not be formed by metamorphic processes. Diabase samples have a green color that is characteristic of chlorite, a low temperature greenschist...grain boundaries of altered olivine and plagioclase (Fig. 3-14c and 13d). Zoning is observed within the oxides indicating alteration; light colored oxides

Kulkeite, a new metamorphic phyllosilicate mineral: Ordered 1∶1 chlorite/talc mixed-layer

NASA Astrophysics Data System (ADS)

Schreyer, W.; Medenbach, O.; Abraham, K.; Gebert, W.; Müller, W. F.

1982-09-01

Kulkeite occurs as platy, colorless, porphyroblastic, single crystals up to 2 mm in size in a low-grade dolomite rock associated with a Triassic meta-evaporite series at Derrag, Tell Atlas, Algeria, It is associated with sodian aluminian talc, unusual chlorite polytypes, and both K and Na phlogopite. Kulkeite is optically biaxial, negative, n x=1.552, n y=1.5605, n z=1.5610, 2Vz=24° (obs.). Based on microprobe analysis the empirical formula is (Na0.38K0.01Ca0.01)(Mg8.02Al0.99)[Al1.43Si6.57O20](OH)10 with some variation in Na, Si, and tetrahedral Al. The crystals are monoclinic with a=5.319(1), b=9.195(2), c=23.897(10) Å, β=97° 1(3)'; Z=2; the calculated density is 2.70 g cm-3. The four strongest lines in the X-ray powder pattern are (d, I, hkl): 7.90, 100, 003; 1.533, 100, 060; 7.42, 80, 002; 3.38, 80, 007; the 001 reflection with 23.7 Å has intensity 10. Transmission electron microscopy confirms the nature of a regular 1∶1 mixed-layer, which consists of 14 Å chlorite (clinochlore) sheets alternating with sheets of one-layer (9.5 Å) talc characterized by the lattice substitution NaAl→Si just as in the talc occurring as a discrete mineral co-existing with kulkeite. Kulkeite is intergrown with lamellae of clinochlore that represent two-layer and five-layer (70 Å) polytypes with optical birefringence exceeding the normal value for clinochlore by a factor of 3. The origin of kulkeite is due to low-grade metamorphism with temperatures probably not exceeding 400° C. As the clinochlore lamellae and sodian aluminian talc are found in mutual contact, kulkeite seems to represent a metastable mineral at least during the latest phase of metamorphism. However, at an earlier stage, prior to clinochlore formation, kulkeite might have been stable, and the incorporation of Na and Al into its talc component could indeed be the decisive factor for the formation of the mixed-layer.

A Reactive Transport Model for Marcellus Shale Weathering

NASA Astrophysics Data System (ADS)

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 factors affecting chemical weathering of the Marcellus shale in the shallow subsurface. This study documents the utility of reactive transport modeling for complex subsurface processes. Such modelling could be extended to understand interactions between injected fluids and Marcellus shale gas reservoirs at higher temperature and pressure.

Pressure Solution Creep and Textural Softening in Greenschist Facies Phyllonites

NASA Astrophysics Data System (ADS)

Wintsch, R. P.; Attenoukon, M.; Kunk, M. J.; McAleer, R. J.; Wathen, B.; Yi, D.

2016-12-01

We have found evidence for dissolution-precipitation creep (DPC) in phyllites and phyllonites naturally deformed at greenschist facies conditions. Since the experiments of Kronenberg et al. (1990) and Mares and Kronenberg (1993) micas are known to be among the weakest of rock-forming minerals. They deform by dislocation glide in their basal plane and when these micas are aligned and contiguous in an orientation favorable for glide they tend to localize strain into shear zones. Therefore, these closed-system experiments suggest that dislocation glide should be the dominant deformation mechanism in mica-rich shear zones from near surface through greenschist facies conditions. In contrast, in naturally deformed rocks we have found strong textural and chemical evidence that micas deform by dissolution-precipitation creep in phyllites at upper and lower greenschist facies conditions. In the Littleton Formation (N.H.) we find retrograde muscovite (pg5)-rich folia (Sn) truncating amphibolite facies Na-rich muscovite and biotite grains that define earlier foliations. Na-rich muscovite grains are also selectively replaced along crenulation axes and boudin necks where plastic and elastic strain are highest. In biotite grade regional metamorphic rocks in the Tananao schist of Taiwan muscovite-rich folia (Sn) truncate crenulated muscovite-biotite schists at high angles. In still lower (chlorite) grade phyllonitic fault zones marking terrane boundaries in southern New England (East Derby shear zone) and in Taiwan (Daugan shear zone) crenulated older fabrics are cut by new undeformed muscovite grains in chlorite-free planar folia. Further evidence for recrystallization rather than dislocation glide comes from the 40Ar/39Ar ages of muscovite in the new Sn folia younger than the age of the truncated folia. The younger ages in each case demonstrate that recrystallization was activated at lower shear stresses than dislocation glide, and that the recrystallization occurred at lower greenschist facies conditions below the closure temperature for diffusion of argon in muscovite. The increase in muscovite/chlorite ratios and change in microchemistry of Sn muscovite, the truncating microstructures, and isotopic results are all incompatible with deformation by dislocation creep.

Past environmental/climatic changes in the northern part of the South China Sea, input from multi-proxy analysis of core MD12-3432

NASA Astrophysics Data System (ADS)

Chen, Quan; Kissel, Catherine; Liu, Zhifei

2017-04-01

In the South China Sea, the magnetic component of marine sediment is a powerful recorder of paleoenvironmental changes linked to the regional and global climate. Based on the knowledge of the sedimentary signature of the potential sources for terrigenous sediments, the composition of marine sediments can be used to decipher the different mechanisms, forcing, and transport vectors. We report here the analysis of the magnetic properties combined with sortable silt and clay mineralogy of a 51 m long sedimentary sequence retrieved from the northern South China Sea and covering the last 400 ka. Magnetic minerals with different coercivities (magnetite, pyrrhotite and hematite) are mixed in the sequence and their relative concentration varies with time. Glacial low sea-levels reduce the land-site distance and they are illlustrated by higher concentrations in magnetites and iron-sulfides (pyrrhotite) related to the sediments previously deposited on the continental shelf and re-worked by the river. This is accompanied by increasing kaolinite content within the clay assemblage (Pearl River signature) and by coarser grains. Superimposed to this eccentricity periodicity, hematite content and smectite/(illite+chlorite) ratio present a predominant precession periodicity synchronous with the northern hemisphere summer insolation changes and therefore with that of the East Asian summer monsoon. Events of high hematite content, in phase with finer grains, coincide with precession lows, while smectite/(illite+chlorite) ratio is maximum during precession highs. Knowing that smectite is mainly produced by contemporaneous chemical weathering intensity in Luzon, we use the smectite/(illite+chlorite) ratio as a tracer for increasing weathering rate in Luzon, in turn related to enhanced East Asian summer monsoon. Hematite is not produced in large amount on adjacent lands and its association with fine sediment grains suggests that its periodic supply is related to the eolian dust transported from the Central China deserts to the studied site. Higher hematite content at this latitude may therefore be used as a tracer for weak East Asian summer monsoon intensity.

Geology and preliminary hydrogeologic characterization of the cell-house site, Berlin, New Hampshire, 2003-04

USGS Publications Warehouse

Degnan, James R.; Clark, Stewart F.; Harte, Philip T.; Mack, Thomas J.

2005-01-01

At the cell-house site, thin, generally less than 20-foot thick overburden, consisting of till and demolition materials, overlies fractured crystalline bedrock. Bedrock at the site consists of gneiss with thin discontinuous lenses of chlorite schist and discontinuous tabular pegmatite. Two distinct fracture domains, with principal trends to the west and northwest, and to the north, overlap near the site. The cell-house site shows principal trends common to both domains. Gneiss is the most abundant rock at the site. Steeply dipping fractures within the gneiss terminate on subhorizontal contacts with pegmatite and on moderately dipping contacts with chlorite schist. Steeply northwest-dipping en Echelon fracture zones, parallel joint zones, and silicified brittle faults show consistent strikes to the northeast. Gently east-dipping to subhorizontal fractures, sub-parallel to gneissosity, strike northeast. The impermeable cap, barrier wall, and bedrock surface topography affect ground-water flow in the overburden. There is relatively little ground-water flow in the overburden in the capped area and a poor hydraulic connection between the overburden and the underlying bedrock over most of the site. The overburden beneath the cap may receive inflow through or beneath the barrier wall, or by flow through vertical fractures in the underlying bedrock beneath the barrier wall. The bedrock aquifer near the river is well connected to the river and head difference in the bedrock across the site are large (greater than 13 ft). Horizontal hydraulic conductivities of 0.2 to 20 ft/d were estimated for the bedrock. Individual fractures or fracture zones likely have hydraulic conductivities greater than the bulk rock. Subhorizontal fractures occur at pegmatite contacts or along chlorite schist lenses and may serve as ground-water conduits to the steeply dipping fractures in gneiss. The effective hydraulic conductivity across the site is likely to be in the low range of the estimated values (0.2 ft/d). Ground water discharges to the river from the bedrock aquifer and is greatest during periods of large river stage fluctuations.

Hydrothermal Alteration of the Mt Unzen Conduit (Shimabara/Japan)

NASA Astrophysics Data System (ADS)

Yilmaz, T. I.; Mayer, K.; Hess, K. U.; Janots, E.; Gilg, H. A.; Dingwell, D. B.

2016-12-01

Investigations were carried out on hydrothermally altered coherent dacitic dykes samples from (USDP-4) drill core at Mt Unzen stratovolcano (Shimabara/Japan). XRF, XRD, EMPA, and C-O-isotope analysis led to insights concerning chemistry, mineralogy, and intensity of alteration as well as the origin of carbonate-precipitating fluids. Additionally a textural characterization of the occurring replacement features in the magma conduit zone was performed. The occurrence of the main secondary phases such as chlorite, pyrite, carbonates, and R1 (Reichweite parameter) illite-smectite indicate a weak to moderate propylitic to phyllic hydrothermal alteration. The dacitic samples of the dykes show different hydrothermal alteration features: (i) carbonate pseudomorphs after hornblende as well as core and zonal textures due to replacement of plagioclase by R1 illite-smectite, (ii) colloform banded fracture fillings and fillings in dissolution vugs, and (iii) chlorite and R1 illite-smectite in the groundmass. Carbonates in fractures comprise iron-rich dolomite solid solutions ("ankerite") and calcite. Isotopic values of d13Cvpdb = -4.59 ± 0.6‰ and d18Ovpdb = -21.73 ± 0.5‰ indicate a hydrothermal-magmatic origin for the carbonate formation. The chlorite-carbonate-pyrite index (CCPI) and the Ishikawa alteration index (AI), applied to the investigated samples show significant differences (CCPI=52.7-57.8; AI=36.1-40.6) indicating their different degree of alteration. According to Nakada et al., 2005, the C13 to C16 dykes represent the feeder dyke from the latest eruption (1991-1995) whereas C8 represents an earlier dyke feeder dyke from an older eruption. Weakest conduit alteration, which was obtained in samples C16-1-5 and C13-2-5, correlates with the alteration degree of the pristine dome rocks. Highest CCPI value was determined for sample C14-1-5 and the highest AI value was determined for sample C15-2-6. The degrees of alteration do not indicate highest alteration of the samples C8-1-2 and C8-2-1 from the older dykes.

Role of clay minerals in the transportation of iron

USGS Publications Warehouse

Carroll, D.

1958-01-01

The clay minerals have iron associated with them in several ways: 1. (1) as an essential constituent 2. (2) as a minor constituent within the crystal lattice where it is in isomorphous substitution and 3. (3) as iron oxide on the surface of the mineral platelets. Nontronite, "hydromica," some chlorites, vermiculite, glauconite and chamosite contain iron as an essential constituent. Kaolinite and halloysite have no site within the lattice for iron, but in certain environments iron oxide (goethite or hematite) is intimately associated as a coating on the micelles. Analyses of clay minerals show that the content of Fe2O3 varies: 29 per cent (nontronite), 7??3 per cent (griffithite), 4.5 per cent ("hydromica"), 5.5 per cent (chlorite), 4 per cent (vermiculite) and 18 per cent (glauconite). The FeO content is: 40 per cent (chamosite), 7.8 per cent (griffithite), 1-2 per cent ("hydromica"), 3 per cent (glauconite) and 2 per cent (chlorite). The iron associated with the clay minerals remains stable in the environment in which the minerals occur, but if either pH or Eh or both are changed the iron may be affected. Change of environment will cause: 1. (1) removal of iron by reduction of Fe3+ to Fe2+; 2. (2) ion-exchange reactions; 3. (3) instability of the crystal lattice. Experiments using bacterial activity to produce reducing conditions with kaolinite and halloysite coated with iron oxides and with nontronite in which ferric iron is in the octahedral position within the lattice showed that ferric oxide is removed at Eh +0??215 in fresh water and at Eh +0.098 in sea water. Hematite, goethite, and indefinite iron oxides were removed at different rates. Red ferric oxides were changed to black indefinite noncrystalline ferrous sulphide at Eh -0.020 but reverted to ferric oxide under oxidizing conditions. Nontronite turned bright green under reducing conditions and some of the ferrous iron remained within the lattice on a return to oxidizing conditions. Bacterial activity seems to be necessary for maintaining reducing conditions in the environments studied. ?? 1958.

Development of weathering profile of a forest hillslope in clay-rich sedimentary system

NASA Astrophysics Data System (ADS)

Nicklas, R. W.; Kim, H.; Bishop, J. K.; Rempe, D. M.

2012-12-01

Hillslopes are an essential element to the understanding of landscape evolution, storm flow generation and biogeochemical processes. Since 2008, extensive studies of climate variables, vegetation, soil moisture, subsurface hydrology, and water chemistry have taken place at a small forested hillslope, "Rivendell", at the Angelo Coast Range Reserve located at the headwaters of the Eel River, California. Here we report on the signature of weathering processes through analysis of core and soil samples collected during well drilling campaigns. Core samples from multiple depths at four wells (at creek edge, mid-slope, up-slope, and ridge-top) were selected and include 1) soil; 2) unsaturated fractured/ weathered zone; 3) zone of seasonal water table fluctuation within weathered bedrock; and 4) chronically saturated fresh bedrock zone. We also include soil samples from a groundwater seep located at the toe of the slope. The mineralogy of these samples was identified using X-ray diffraction. Samples were analyzed for salt and Ca(Mg)CO3 concentrations, and cation exchange capacity using Milli-Q water and acetic acid extraction and BaCl2-NH4Cl treatments, respectively. To further quantify the mineral dissolution and secondary mineral precipitation, a sequential extraction of trace metals were conducted - 1) exchangeable using MgCl2; 2) bound to carbonates using NaOAc; 3) bound to Fe-Mn oxides using NH2OH HCl; and 4) bound to organic matters using H2O2 and HNO3. The total elemental contents were determined using HF-HNO3-HClO4 dissolution. The mineralogy of the fresh bedrock zone showed similar patterns throughout the site -for clay minerals, chlorite, illite, interstratified illite/smectite were dominant; K-feldspar dominated the primary minerals. Shallow (<30 cm) soils had kaolinite, and chlorite was absent in some samples. CaCO3 was also predominantly found in the fresh bedrock zone and progressively increased with depth. The depletion profile of major cations (Ca, Na, Mg, K, and Si) and trace metals (Fe, Mn and Al) show the mineral dissolution fronts. K-feldspar, chlorite and CaCO3 dissolution and secondary mineral precipitation are thus the major processes that are critical to the interpretation of groundwater chemistry.

Microstructure and seismic anisotropy of phyllite from Geumseongri Formation and Munjuri Formation in Korea

NASA Astrophysics Data System (ADS)

Han, S.; Jung, H.

2016-12-01

Mica is a mineral group that shows the strongest seismic anisotropy among the minerals comprising continental crust of the Earth. It is also noteworthy that alignment of mica can strongly affect magnitude and symmetry of seismic anisotropy if a seismic wave passes through a rock composed of mica more than 20-40%. Thus, it is highly necessary to analyze mica-rich rocks to investigate the origin of seismic anisotropy observed in continental crust. In this study, muscovite-quartz phyllites from Geumseongri and Munjuri Formation in Korea were analyzed using Electron Backscattered Diffraction (EBSD) to measure lattice preferred orientation (LPO) of minerals. The samples are mainly composed of muscovite, quartz, albite, chlorite, and biotite with minor calcite and rutile. The EBSD analysis showed that the muscovite [001] axis was strongly aligned normal to the foliation while both [100] and [010] axes were dispersed parallel to the foliation. Chlorite and biotite also exhibited similar LPO except for the chlorite [001] axis in the sample 2619, dispersed normal to the lineation. LPOs of quartz were weak in most samples. The albite (010) pole in the sample 2363M and (001) pole in the sample 2364Q were aligned normal to the foliation. Seismic anisotropy was calculated based on the LPO and modal composition of the specimens. The anisotropy of P-wave (Vp) for quartz was in the range of 4.3 - 9.3% and 3.3 - 6.7% for albite. The maximum shear wave anisotropy (AVs) was in the range of 5.3 - 11.2% for quartz and 3.9 - 5.4% for albite. The Vp anisotropy and maximum AVs anisotropy of mica were in the range of 19.3 - 53.4% and 11.6 - 62.9%, respectively, which are much larger than those of other minerals. As a result, The Vp and maximum AVs anisotropy for whole rock were in the range of 11.8 - 44% and 11.6 - 51.8%, respectively. These results show that modal composition and alignment of mica mainly control the magnitude and symmetry of seismic anisotropy.

Development of a Portable Binary Chlorine Dioxide Generator for Decontamination

DTIC Science & Technology

2010-03-01

chlorine dioxide forms slowly from chlorite solutions through either acid release or a radical chain reaction that we observed at neutral pH. Task 7... Chlorine dioxide and water in methanol - no agent control F. 5.25% Bleach G. Methanol only 3.0 PROCEDURES 3.1 METHOD VALIDATION The reaction...error range in gas chromatography measurements. For the chlorine dioxide containing samples, mass spectra were analyzed to determine potential

Mineralogical textural and compositional data on the alteration of basaltic glass from Kilauea, Hawaii to 300 degrees C: Insights to the corrosion of a borosilicate glass waste-form. [Yucca Mountain Project

DOE Office of Scientific and Technical Information (OSTI.GOV)

Smith, D.K.

1990-01-01

Mineralogical, textural and compositional data accompanying greenschist facies metamorphism (to 300{degrees}C) of basalts of the East Rift Zone (ERZ), Kilauea, Hawaii may be evaluated relative to published and experimental results for the surface corrosion of borosilicate glass. The ERZ alteration sequence is dominated by intermittent palagonite, interlayered smectite-chlorite, chlorite, and actinolite-epidote-anhydrite. Alteration is best developed in fractures and vesicles where surface reaction layers root on the glass matrix forming rinds in excess of 100 microns thick. Fractures control fluid circulation and the alteration sequence. Proximal to the glass surface, palagonite, Fe-Ti oxides and clays replace fresh glass as the surfacemore » reaction layer migrates inwards; away from the surface, amphibole, anhydrite, quartz and calcite crystallize from hydrothermal fluids in contact with the glass. The texture and composition of basaltic glass surfaces are similar to those of a SRL-165 glass leached statically for sixty days at 150 {degrees}C. While the ERZ reservoir is a complex open system, conservative comparisons between the alteration of ERZ and synthetic borosilicate glass are warranted. 31 refs., 2 figs.« less

Fracturing, fluid-rock interaction and mineralisation during the seismic cycle along the Alpine Fault

NASA Astrophysics Data System (ADS)

Williams, Jack N.; Toy, Virginia G.; Smith, Steven A. F.; Boulton, Carolyn

2017-10-01

The Alpine Fault has a <50 m wide geochemically distinct hanging-wall alteration zone. Using a combination of petrological and cathodoluminescence (CL) microscopy, Energy Dispersive Spectroscopy and X-ray diffraction, we document the habitat and mineralising phases of macro- and micro-fractures within the alteration zone using samples derived from outcrop and the Deep Fault Drilling Project. Veins predominantly contain calcite, chlorite, K-feldspar or muscovite. Gouge-filled fractures are also observed and reflect filling from mechanical wear and chlorite mineralisation. CL imaging suggests that each calcite vein was opened and sealed in one episode, possibly corresponding to a single seismic cycle. The thermal stability of mineralising phases and their mutually cross-cutting relationships indicates a cyclic history of fracture opening and mineralisation that extends throughout the seismogenic zone. Cataclasites contain intragranular veins that are hosted within quartzofeldspathic clasts, as well as veins that cross-cut clasts and the surrounding matrix. Intragranular calcite veins formed prior to or during cataclasis. Cross-cutting veins are interpreted to have formed by fracturing of relatively indurated cataclasites after near-surface slip localisation within the Alpine Fault's principal slip zone gouges (PSZs). These observations clearly demonstrate that shear strain is most localised in the shallowest part of the seismogenic zone.

Effects of CO 2 on mechanical variability and constitutive behavior of the Lower Tuscaloosa formation, Cranfield Injection Site, USA

DOE PAGES

Rinehart, Alex J.; Dewers, Thomas A.; Broome, Scott T.; ...

2016-08-25

We characterize geomechanical constitutive behavior of reservoir sandstones at conditions simulating the “Cranfield” Southeast Regional Carbon Sequestration Partnership injection program. From two cores of Lower Tuscaloosa Formation, three sandstone lithofacies were identified for mechanical testing based on permeability and lithology. These include: chlorite-cemented conglomeratic sandstone (Facies A); quartz-cemented fine sandstone (Facies B); and quartz- and calcite-cemented very fine sandstone (Facies C). We performed a suite of compression tests for each lithofacies at 100 °C and pore pressure of 30 MPa, including hydrostatic compression and triaxial tests at several confining pressures. Plugs were saturated with supercritical CO 2-saturated brine. Chemical environmentmore » affected the mechanical response of all three lithofacies, which experience initial plastic yielding at stresses far below estimated in situ stress. Measured elastic moduli degradation defines a secondary yield surface coinciding with in situ stress for Facies B and C. Facies A shows measurable volumetric creep strain and a failure envelope below estimates of in situ stress, linked to damage of chlorite cements by acidic pore solutions. Furthermore, the substantial weakening of a particular lithofacies by CO 2 demonstrates a possible chemical-mechanical coupling during injection at Cranfield with implications for CO 2 injection, reservoir permeability stimulation, and enhanced oil recovery.« less

DOE Office of Scientific and Technical Information (OSTI.GOV)

Huntsman, J.R.

Eastern slate belt lithologies in the central Flowers quadrangle consist of metavolcanic and metasedimentary rocks. Very fine-grained quartz-white mica phyllite containing narrow, discontinuous layers of thinly laminated chlorite-rich rock and fine-grained, thinly layered, feldspar crystal felsic metatuff comprise the dominant, mappable units consistent across the quadrangle. An increase in grain size accompanied by a replacement of chlorite-rich lithologies with biotite [+-] garnet assemblages suggest metamorphic grade increases towards the western half of the quadrangle (quartz-muscovite schist and biotite-quartz-muscovite-feldspar gneiss). An early, northeast-trending foliation (050[degree] to 060[degree]) dipping moderately to steeply southeast persists across the quadrangle and is axial planar tomore » tight to isoclinal, recumbent to moderately inclined folds. Later non-coaxial folding produced steeply plunging, northerly trending (000[degree] to 020[degree]), open, asymmetric structures verging towards the east/southeast. Shear zones formed locally along the axial trend of these later folds and produced protomylonitic to mylonitic ( ) fabrics. Map patterns and cross-sectional interpretations are best explained by modification of zig-zag fold interference patterns. Thin section examination reveals garnets growing across the early axial planar foliation. The observed increase in metamorphic grade across the quadrangle matches the regional Alleghanian prograde event and constrains relative timing of observed deformational fabrics. Noticeably absent are regional, late-stage upright folds.« less

Elucidation of the mechanism of enzymatic browning inhibition by sodium chlorite.

PubMed

He, Qiang; Luo, Yaguang; Chen, Pei

2008-10-15

Sodium chlorite (SC) is a well known anti-microbial agent and its strong inhibitory effect on enzymatic browning of fresh-cut produce has recently been identified. We investigated the effect of SC on polyphenol oxidase (PPO) and its substrate, chlorogenic acid (CA), as it relates to the mechanisms of browning inhibition by SC. Results indicate that the browning reaction of CA (1.0mM) catalyzed by PPO (33U/mL) was significantly inhibited by 1.0mM SC at pH 4.6. Two PPO isoforms were identified by native polyacrylamide gel electrophoresis, and both were inactivated by SC (3.0mM). This suggests that SC serves as a PPO inhibitor to prevent enzymatic browning. Furthermore, the effect of SC on the stability of CA in both acidic (pH 4.5) and basic conditions (pH 8.3) was studied by UV-Vis scan and LC-MS analysis. The results showed that at the presence of SC (3.0mM), CA (0.1mM) degraded to quinic acid and caffeic acid as well as other intermediates. Hence, the anti-browning property of SC can be attributed to the two modes of action: the inactivation of polyphenol oxidase directly and the oxidative degradation of phenolic substrates. Published by Elsevier Ltd.

Immature pea seeds: effect of storage under modified atmosphere packaging and sanitation with acidified sodium chlorite.

PubMed

Collado, Elena; Venzke Klug, Tâmmila; Martínez-Sánchez, Ascensión; Artés-Hernandez, Francisco; Aguayo, Encarna; Artés, Francisco; Fernández, Juan A; Gómez, Perla A

2017-10-01

Appropriate sanitation is a priority for extending the shelf life and promoting the consumption of immature pea seeds, as processing accelerates quality deterioration and microbial growth. The combined effect of disinfection with acidified sodium chlorite (ASC) or sodium hypochlorite (SH) and packaging under a passive modified atmosphere (MAP) at 1 or 4 °C on quality was analysed. After 14 days, greenness and vitamin C had decreased, especially in the SH-disinfected samples. Total phenols and antioxidant capacity were not affected by disinfection. Proteins levels fell by around 27%, regardless of the sanitizer and storage temperature. Compared with the initial microbial load, samples stored at 1 °C showed an increase of 1 log CFU g -1 in psychrophiles when treated with SH, whereas no increase of note occurred with ASC. In general, microbial counts were always below 3 log CFU g -1 for all the treatments. Immature pea seeds could be stored for 14 days at 1-4 °C under MAP with only minor quality changes. Disinfection with ASC resulted in better sensory quality, higher content of vitamin C and lower psychrophile counts. More research is needed to analyse the effect of these treatments on other quality parameters. © 2017 Society of Chemical Industry. © 2017 Society of Chemical Industry.

Re-evaluation of the petrogenesis of the Proterozoic Jabiluka unconformity-related uranium deposit, Northern Territory, Australia

NASA Astrophysics Data System (ADS)

Polito, Paul A.; Kurt Kyser, T.; Thomas, David; Marlatt, Jim; Drever, Garth

2005-11-01

The world class Jabiluka unconformity-related uranium deposit in the Alligator Rivers Uranium Field, Australia, contains >163,000 tons of contained U3O8. Mineralization is hosted by shallow-to-steeply dipping basement rocks comprising graphitic units of chlorite-biotite-muscovite schist. These rocks are overlain by flat-lying coarse-grained sandstones belonging to the Kombolgie Subgroup. The deposit was discovered in 1971, but has never been mined. The construction of an 1,150 m decline into the upper eastern sector of the Jabiluka II deposit combined with closely spaced underground drilling in 1998 and 1999 allowed mapping and sampling from underground for the first time. Structural mapping, drill core logging and petrographic studies on polished thin sections established a detailed paragenesis that provided the framework for subsequent electron microprobe and X-ray diffraction, fluid inclusion, and O-H, U-Pb and 40Ar/39Ar isotope analysis. Uranium mineralization is structurally controlled within semi-brittle shears that are sub-conformable to the basement stratigraphy, and breccias that are developed within the hinge zone of fault-related folds adjacent to the shears. Uraninite is intimately associated with chlorite, sericite, hematite ± quartz. Electron microprobe and X-ray diffraction analysis of syn-ore illite and chlorite indicates a mineralization temperature of 200°C. Pre- and syn-ore minerals extracted from the Kombolgie Subgroup overlying the deposit and syn-ore alteration minerals in the Cahill Formation have δ18Ofluid and δ D fluid values of 4.0±3.7 and -27±17‰, respectively. These values are indistinguishable from illite separates extracted from diagenetic aquifers in the Kombolgie Subgroup up to 70 km to the south and east of the deposit and believed to be the source of the uraniferous fluid. New fluid inclusion microthermometry data reveal that the mineralising brine was saline, but not saturated. U-Pb and 207Pb/206Pb ratios of uraninite by laser-ablation ICP-MS suggest that massive uraninite first precipitated at ca. 1,680 Ma, which is coincident with the timing of brine migration out from the Kombolgie Subgroup as indicated by 40Ar/39Ar ages of 1,683±11 Ma from sandstone-hosted illite. Unmineralized breccias cemeted by chlorite, quartz and sericite cross-cut the mineralized breccias and are in turn cut by straight-sided, high-angle veins of drusy quartz, sulphide and dolomite. U-Pb and 207Pb/206Pb ratios combined with fluid inclusion and stable isotope data indicate that these post-ore minerals formed when mixing between two fluids occurred sometime between ca. 1,450 and 550 Ma. Distinct 207Pb/206Pb age populations occur at ca. 1,302±37, 1,191±27 and 802±57 Ma, which respectively correlate with the intrusion of the Maningkorrirr/Mudginberri phonolitic dykes and the Derim Derim Dolerite between 1,370 and 1,316 Ma, the amalgamation of Australia and Laurentia during the Grenville Orogen at ca. 1,140 Ma, and the break-up of Rodinia between 1,000 and 750 Ma.

Dehydration-driven topotaxy in subduction zones

NASA Astrophysics Data System (ADS)

Padrón-Navarta, José Alberto; Tommasi, Andréa; Garrido, Carlos J.

2014-05-01

Mineral replacement reactions play a fundamental role in the chemistry and the strength of the lithosphere. When externally or internally derived fluids are present, interface-coupled dissolution-precipitation is the driving mechanism for such reactions [1]. One of the microstructural features of this process is a 3D arrangement of crystallographic axes across internal interfaces (topotaxy) between reactant and product phases. Dehydration reactions are a special case of mineral replacement reaction that generates a transient fluid-filled porosity. Among others, the dehydration serpentinite is of special relevance in subduction zones because of the amount of fluids involved (potentially up to 13 wt.%). Two topotatic relationships between olivine and antigorite (the serpentine mineral stable at high temperature and pressure) have been reported in partially hydrated mantle wedge xenoliths [2]. Therefore, if precursor antigorite serpentine has a strong crystallographic preferred orientation (CPO) its dehydration might result in prograde peridotite with a strong inherited CPO. However for predicting the importance of topotactic reactions for seismic anisotropy of subduction zones we also need to consider the crystallization orthopyroxene + chlorite in the prograde reaction and, more importantly, the fact that this dehydration reaction produces a transient porosity of ca. 20 % vol. that results in local fluctuations of strain during compaction and fluid migration. We address this issue by a microstructural comparison between the CPO developed in olivine, orthopyroxene and chlorite during high-pressure antigorite dehydration in piston cylinder experiments (at 750ºC and 20 kbar and 1000ºC and 30 kbar, 168 h) and that recorded in natural samples (Cerro del Almirez, Betic Cordillera, Spain). Experimentally developed CPOs are strong. Prograde minerals show a significant inheritance of the former antigorite foliation. Topotactic relations are dominated by (001)atg//(100)ol// (100)opx//(001)chl. The relation [010]atg// [001]ol //[001]opx can also be inferred but it is weaker. Similar topotactic relations are observed in the Cerro del Almirez samples, but the CPOs are weaker and more complex. The complexity arises from constant interfacial angles and systematic low-index interfacial contacts between orthopyroxene-olivine-chlorite (e.g. (001)chl // (100)opx). As a consequence the inheritance from the antigorite serpentinite is partially obliterated. Compaction-related microstructural features are also present including: (1) smooth bending of the former foliation and diffuse olivine veinlets perpendicular to it, (2) gradual crystallographic misorientation (up to 15º) of prismatic enstatite due to buckling, (3) localized orthoenstatite(Pbca)/low clinoenstatite (P21/c) inversion, and (4) brittle fracturing of prismatic enstatite wrapped by plastically deformed chlorite. These observations suggest that topotactic crystrallographic relations are dominant in undrained systems, but that the mechanisms allowing for compaction and fluid draining significantly affect the final texture in drained systems. Because the second case prevails in subduction zones, compaction mechanisms need to be better understood for modelling the development of CPOs after foliated protoliths in the slab and the mantle wedge. [1] Putnis, A., 2009. Reviews in Mineralogy and Geochemistry 70, 87-124. [2] Boudier, F., et al. 2010 J. Petrology 51, 495-512.

Geologic map of the Dusar area, Herat Province, Afghanistan; Modified from the 1973 original map compilations of V.I. Tarasenko and others

USGS Publications Warehouse

Tucker, Robert D.; Stettner, Will R.; Masonic, Linda M.; Bogdanow, Anya K.

2017-10-24

The geologic maps and cross sections presented in this report are redrafted and modified versions of the Geologic map and map of useful minerals of the Dusar area (scale 1:50,000) and Geologic sketch map of the Dusar and Namak-sory ore occurrences (scale 1:10,000), located in the Herat Province, Afghanistan. The original maps and cross sections are contained in unpublished Soviet report no. 0290 (Tarasenko and others, 1973) prepared in cooperation with the Ministry of Mines and Industries of the Royal Government of Afghanistan, in Kabul during 1973 under contract no. 50728. The redrafted maps and cross sections (modified from Tarasenko and others, 1973) illustrate the geological structure and mineral occurrences of the Dusar copper-gold-silver-lead-zinc prospect area of western Afghanistan, located within the Dusar-Shaida copper and tin area of interest (AOI), Herat Province, Afghanistan.Mineralization in the Dusar area is hosted within Early Jurassic to Early Cretaceous stratified volcanic and sedimentary rocks associated with numerous diabase and gabbro-diabase intrusive bodies and is generally near a major northeast-trending system of faults and quartz veins. Host rocks consist of quartz keratophyre and quartz-feldspar porphyry, with layers of schist, phyllite, and quartz-chlorite and chlorite-sericite slate; and limestone and shale, with schist and carbonate-chlorite and chlorite slate. Known mineralization includes an extensive quartz vein system, shown on the map as the “northern occurrence,” as well as the Dusar and Namak-sory gossan zones, interpreted to have formed from remnant pyrite mineralization. The veins of the northern occurrence and their altered host rocks are known to contain anomalous to economic concentrations of precious and base metals, with concentrations locally in excess of 2 parts per million gold, 100 parts per million silver, 5 percent copper, and 1 percent lead. These veins occur in swarms, and are hosted along structures that are approximately concordant with the plane of the metamorphic fabric. The veins consist mostly of quartz, with minor carbonate and sulfide minerals, and display weak alteration halos along their margins. The gossans are locally anomalous in these metals, but their size and extent makes them attractive exploration targets for potential massive sulfide mineralization.The Dusar gossan zone is a massive, ochreous, and siliceous limonitic rock, approximately 2,200 meters long, 30 to 250 meters wide, and 2.0 to 7.2 meters thick. Drilling below the Dusar gossan intersected a siliceous, sericitic, and limonitic rock underlain by quartz keratophyre with abundant disseminated pyrite. Mineralized sections grade 0.06 weight percent copper and up to 0.05 weight percent zinc. The Namak-sory gossan zone contains a similar deposit with anomalous concentrations of copper, zinc, and gold.The redrafted maps and cross sections reproduce the topology of rock units, contacts, and faults of the original Soviet maps and cross sections, and include minor modifications based on examination of the originals and observations made during two brief field visits by USGS staff in August, 2010, and June, 2013.

Spinifex-textured komatiites in the south border of the Carajas ridge, Selva Greenstone belt, Carajás Province, Brazil

NASA Astrophysics Data System (ADS)

Siepierski, Lincoln; Ferreira Filho, Cesar Fonseca

2016-03-01

Spinifex-textured komatiites in the Selva greenstone belt are the first unequivocal examples of komatiites in the Transition Subdomain of the Carajás Mineral Province. Outcrops of spinifex-textured komatiites, located ∼1.5 km to the south of the Carajás ridge, were discovered during regional exploration for Ni-Cu-(PGE) sulfide deposits by VALE. They are associated with a 3.8 km long unit consisting of variable types of ultramafic rocks (talc schist, serpentinite and spinifex-textured komatiite). This ultramafic unit follows the steep dipping NW-SE trending Selva greenstone belt composed mainly by quartz-chlorite schists (interpreted as metasediments) and chlorite-actinolite schists (interpreted as metabasalts). Greenschist facies metamorphic parageneses characterize all rock types in the Selva greenstone belt. The komatiitic rocks in the Selva belt comprise a sequence of flows consisting of an upper spinifex-textured layer and a lower olivine cumulate layer. Although the spinifex and cumulus textures are well preserved in the field, the primary mineralogy of the komatiites has been completely replaced by greenschist facies metamorphic minerals. Platy olivine spinifex texture, consisting of an array of roughly parallel olivine plates, and random spinifex texture, consisting of randomly oriented olivine plates, are the most common primary volcanic textures in komatiites in the Selva greenstone belt. Platy and random spinifex texture is defined by former plates of olivine replaced by serpentine with minor actinolite, chlorite and magnetite, alternating with former matrix replaced by abundant actinolite and minor chlorite, talc, serpentine, and magnetite. The domains between olivine plates in both platy and random spinifex-textured rocks contain irregular arrays of fine-grained parallel crystals, representing primary fine-grained "quench" clinopyroxene crystals replaced by actinolite. Spinifex-textured komatiites have MgO contents bracket between 22.8 and 26.9 wt.%, and cumulate textured komatiites have MgO contents up to 40.6 wt.%. When plotted vs MgO contents, most major and minor elements fall on well-defined linear trends indicating control by olivine fractionation or accumulation. Komatiites from the Selva and Seringa (located in the Rio Maria Domain) belts are Al-undepleted with Al2O3/TiO2 ratios close to 20. Results for CaO, Na2O, and REE suggest that these elements were mobile and their abundances have been modified during metasomatic alteration. REE contents in some samples are very high (up to 40 times primitive mantle values) and REE patterns vary from flat (La/YbMN ∼ 1) to highly enriched in LREE (La/YbMN up to ∼ 10). The REE mobility may be related to hydrothermal alteration associated to Cu-Au mineralization in the region. The identification of spinifex-textured komatiites close to the Carajás Basin suggests the continuation of 3.0-2.9 Ga greenstone belts of the Rio Maria Domain within the Transition Subdomain, and enlarges the area with potential to host komatiite-associated Ni-Cu-PGE deposits.

Palaeoproterozoic Volcanic Massive Sulphides (VMS) in the Lithuanian crystalline basement: evidences for a back-arc tectonic setting

NASA Astrophysics Data System (ADS)

Skridlaite, Grazina; Siliauskas, Laurynas

2014-05-01

In the southwestern part of the East European Craton (EEC), several events of Palaeoproterozoic volcanic arc magmatic activity were recognized in the concealed crystalline basement. In Lithuania, the TTG suites of 1.89 Ga and 1.86-1.84 Ga were later metamorphosed in amphibolite and granulite facies conditions. Remnants of a volcano-sedimentary sequence metamorphosed in green schist and amphibolite facies conditions were discovered in central and southern Lithuania. In southern Lithuania, the upper part of the Lazdijai 13 (Lz13) drilling (at c. 493 m depth) consists of exhalitic quartz chlorite cherts mixed with andesitic rocks. The rocks are impregnated with magnetite in some places replacing calcite. Most of the magnetite grains are overgrown by a dendritic kovelite, which may have formed while magnetite was still in aqueous surrounding. Other accessory minerals are xenotime, zircon, apatite, Sr-Ba sulphates etc. The cherts are underlain by a metaandesite which volcanic structures were obscured by hydrothermal alteration, i.e. the idiomorphic magnetite crystals and porphyritic plagioclase grains were replaced by clay minerals and quartz or muscovite in many places. Thin metamorphosed mudstone layers turned into garnet, biotite (+/-staurolite) and chlorite schists. The rocks were affected by silicification, chloritization, argilitization and carbonatization. Taking into account the rock composition, micro and macro scale alteration zones and absence of breccia, the whole package resembles an outer part of the VMS stockwork. The lower boundary at 526 m is sharp, marked by a quartz vein, below which lies quartz, biotite (+/- chlorite) bearing schist with minor tremolite (former sandstone). It was intensely affected by silicification, and was enriched in Na, K and Ca. Accessory minerals are monazite, xenotime, apatite and detrital zircon. The schist exhibits fine mineral foliation, and is fine-grained. A 4 m thick granitic vein cuts the rock at 654 m depth, below which there are amphibolites with layers or lenses of skarns formed in marbles. Some amphibolites resemble porphyritic basalts. These might be dikes of basalts, which are common for back arc VMS surroundings. The volcano-clastic rock from the Lz13 yielded c. 1.83 Ga and c. 1.80 Ga ages. The whole rock Sm-Nd isotopic composition points towards juvenile origin of the rock (TDM=2.08 Ga, ɛNd (1.9) +1.8). After the comparison of the obtained data set with VMS deposits formed in different environments, it is most likely that the volcano-sedimentary sequence of Lz13 was formed in a back arc tectonic setting. The volcano-sedimentary sequence can be correlated with the 1.83 Ga Oskarshamn-Jönköping Belt (Mansfeld et al., 2005) and the volcano-sedimentary Vetlanda formation (Makowsky and Mansfeld, 2013) in southeastern Sweden. The c. 1.83-1.80 Ga volcanic arc and back-arc system continues from southeastern Sweden through the Baltic Sea to Lithuania. This is a contribution to the Open Access Centre activities Mansfeld, J., Beunk, F.F. and Barling, J., 2005. GFF, 127: 149-157 Makowsky, F., Mansfeld, J., 2013. 31st Nordic Geological Winter Meeting, Lund, Sweden, 89-90.

Fluid-rock interaction controlling clay-mineral crystallization in quartz-rich rocks and its influence on the seismicity of the Carboneras fault area (SE Spain)

NASA Astrophysics Data System (ADS)

Jimenez-Espinosa, R.; Abad, I.; Jimenez-Millan, J.; Lorite-Herrera, M.

2009-04-01

The Carboneras Fault zone is one of the longest fault in the Betic Cordillera (SE Spain) and it would be a good candidate to generate large magnitude earthquakes (Gracia et al., 2006). Seismicity in the region is characterised by low to moderate magnitude events, although large destructive earthquakes have occurred, which reveals significant earthquake and tsunami hazards (Masana et al., 2004). Due to the internal architecture of the fault zone, shear lenses of post-orogenic sediments of Miocene and Pliocene age including marls and sandstones sequences are juxtaposed to the predominant slaty gouges of the Alpine basement. Microcataclasites and gouges of the quartz-rich post-orogenic sediments are also developed as cm- to m-scale bands, allowing the comparison between the deformed materials and their protoliths. Red, yellow and white sandstones and their respective cataclasites can be identified. This communication is concerned with the clay mineral crystallization events in these materials and its possible influence on the seismicity model of the region. The presence of phyllosilicates in fault zones as either neoformed or inherited clays is commonly related with fluid circulation and a mechanically weak fault behaviour (e.g., Wang, 1984). A critical factor for the understanding of the mechanical role of clays in fault rocks is to determine the timing of formation of mineral assemblages and microstructure of fault rocks and protolith. The effects of post-faulting alteration limit inferences about fault behaviour that can be made from exhumed rocks. The Carboneras fault zone provides good opportunities to study mineral processes enhanced by deformation, given that it is located in a region of arid climate and shows outcroppings of quartzitic rocks included in slaty rocks. Combined XRD, optical microscopy and SEM analyses reveal that deformed quartzitic rocks are enriched in phyllosilicates, increasing especially the amount of chlorite. The samples strongly damaged are characterised also by the presence of dolomite and gypsum. The deformation is highly localized, developing phyllosilicate-rich bands highly foliated due to the presence of fine-sized aligned clays (chlorite and mica). In some undeformed lenses of the cataclastic rocks, variable-sized patches of phyllosilicates containing random oriented stacks of chlorite and mica are developed. BSE images reveal that the stacks are made of two intergrown compositional types of chlorite. These results lead to conclude that limited clay growth during faulting occurred. The absence of significant compositional differences between undeformed and deformed phyllosilicates suggests that whereas fluids were present during strike-slip faulting, fluids were not preferentially focused along the quartz-rich rocks of the fault zone by phyllosilicates avoiding the development of the synkinematic clay alteration process. However, clays played an important role for the mechanical behaviour of the quartzitic rocks in the fault zone. Deformation is highly localized in chlorite-rich sandstones. These sandstones show substantial clay crystallization which texture can be related with a hydrothermal origin before strike-slip faulting, likely associated with the volcanic activity of the area leading to form of chlorite/mica patches. These data indicate that, although elevated fluid pressure confined by clay fabric cannot be appealed for the mechanical behaviour of the sandstones of the Carboneras fault, clay fabrics developed during deformation dominated the fault-weakening mechanism. We consider that lubricating properties of phyllosilicates in the quartzitic rocks were an important factor controlling movement mechanisms promoting the predominance of creep as regards seismic stick-slip (Bedrosian et al., 2004) reducing the possibility of larger seismogenic events that nucleate on localized fault planes developed within quartzitic rocks contained within the fault zone. Finally the crystallization of dolomite and gypsum in the highly damaged areas of the microcataclasites could be related with recent low-temperature and high-salinity water circulation episodes, suggesting that cataclasis may control pathways and focus circulation of the current aquifer systems. References Bedrosian, P.A., Unsworth, M.J., Egbert, G.D., Thuerber, C.H. (2004): Geophysical images of creeping segment of the San Andreas Fault: Implications for the role of crustal fluids in the earthquake process. Tectonophysics, 385, 137-158. Gracia, E., Palla, R., Soto, J.I., Comas, M., Moreno, X., Masana, E., Santanach, P., Diez, S., García, M., Dañobeitia, J. & HITS scientific party (2006): Active faulting offshore SE Spain (Alboran Sea): Implications for earthquake hazard assessment in the Southern Iberian Margin. Earth and Planetary Science Letters, 241, 734-749. Masana E., Martínez-Díaz, J.J., Hernández-Enrile, J.L. & Santanach, P. (2004): The Alhama de Murcia fault (SE Spain), a seismogenic fault in a diffuse plate boundary: seismotectonic implications for the Ibero-Magrebian region. J. Geophys. Res., 109, 1-17. Wang, C.Y. (1984): On the constitution of the San Andreas fault zone in central California. J. Geophys. Res., 89, 5858-5866.

Investigation of Cyclodextrin-Enhanced Electrokinetic Soil Remediation. Fate and Transport of Nitroaromatic Contaminants and Cyclodextrin Amendments in Expansive Clays

DTIC Science & Technology

2004-09-01

report increasing adsorption capacity depending on the specific clay type, in the order kaolinite < illite < montmorillonite (11). This finding suggests... kaolinite , illite, and montmorillonite . Finally, there is a wide varia- tion in adsorption constants among the different nitroaromatic compounds...common to micas, chlorites, pyrophyllite, talc, kaolinite , and gibbsite . As is now known, clays typically consist of layered crystalline structures

Post-metamorphic fluid infiltration into granulites from the Adirondack Mountains, USA

NASA Technical Reports Server (NTRS)

Morrison, J.; Valley, John W.

1988-01-01

Post-metamorphic effects in the anorthosites of the Adirondacks, New York were described. Calcite-chlorite-sericite assemblages occur as veins, in disseminated form and as clots, and document retrograde fluid infiltration. These features are associated with late-state CO2-rich fluid inclusions. Stable isotope analyses of calcites indicates that the retrograde fluids interacted with meta-igneous and supracrustal lithologies, but the precise timing of the retrogression is as yet unknown.

Water disinfection agents and disinfection by-products

NASA Astrophysics Data System (ADS)

Ilavský, J.; Barloková, D.; Kapusta, O.; Kunštek, M.

2017-10-01

The aim of this work is to describe factors of water quality change in the distribution network and legislative requirements in Slovakia for disinfectants and disinfection byproducts (DBPs). In the experimental part, the time dependence of the application of the chlorine dioxide and sodium hypochlorite on the formation of some by-products of disinfection for drinking water from WTP Hriňová is studied. We monitored trihalomethanes, free chlorine, chlorine dioxide and chlorites.

The "green stones" of Valtellina and Valchiavenna (central Alps, northern Italy)

NASA Astrophysics Data System (ADS)

Cavallo, Alessandro

2015-04-01

Valtellina and Val Chiavenna (Sondrio, Central Alps, northern Italy) are traditionally areas of production of building and ornamental stones (e.g. Serizzo Ghiandone, Serizzo Valmasino, San Fedelino Granite), and among these the "green stones" have a leading position. These stones had an extensive use in Lombardy, as well as abroad (e.g Switzerland). The "green stones" are related to the two mafic-ultramafic bodies of Valmalenco and Chiavenna, where the two largest quarrying districts of the Province of Sondrio are located. Until the early decades of the XX century, serpentinites (and other lithologies from Valtellina) were also extracted from the erratic boulders of Brianza (north of Milan), but at present time the law protects the few remaining boulders. The extracted and processed materials are various: serpentinites, ophicalcites, soapstones. Even the "Stone of Tresivio", used in the past in important monuments of Valtellina, could be classified among the "green stones" in a broad sense: it is a green chloritic schist with scarce and thin ferriferous calcitic veins, pertaining to the sedimentary "Servino" Formation. In recent times, the ancient quarries of this stone were rediscovered near the homonymous village, a few kilometers from Sondrio. There are also historic reports about other "green stones", used in ancient times, such as the "Stone of Grosio", a chloritic schist, and the "Bormio Prasinite". Currently the extraction and processing of "green stones" occurs mostly in Valmalenco, with 22 active serpentinite quarries and a gross volume of 70000 m3 extracted per year, with a yield of about 50%. The Malenco serpentinite (interpreted as sub-continental mantle rocks) forms a 1-2 km thick tabular body, outcropping over an area of about 170 km2, almost entirely confined within the boundaries of the valley. The antigoritic serpentinites (with variable amounts of olivine, clinopyroxene, chlorite and magnetite) are moderately up to strongly foliated, sometimes folded, and are processed in two main commercial varieties: schistose ("serpentinoscisto") and massive ("serpentino da taglio"). In Valmalenco, the extraction and processing of schistose serpentinites for the production of slabs ("piode", splitted by hand with hammer and chisel), used in roofing and flooring, dates back at least to the XIV century. From the traditional underground extraction, the quarrying activities moved to the modern open-cast extraction in the seventies. The renowned quality of the secular serpentinite roof coverings is related to the excellent physical and mechanical properties, especially the flexural strength (average values around 90-100 MPa), very low porosity and the thaw/freezing resistance. The "massive" serpentinite achieved a special place in the national and international market of ornamental stones: the several extracted varieties (Serpentino Classico, Verde Vittoria, Verde Perlato, Verde Mare, Verde Principe, Verde Torre S. Maria), in addition to the excellent technical properties (flexural strength and thermal properties) that promote specific uses, make these stones much appreciated worldwide (e.g. Bundestag in Berlin, Germany). As part of the "green stones" of Valmalenco, two currently abandoned ophicalcite quarries have been active in the recent past. The extraction and processing of soapstone ("pietra ollare" or "pietra laugera", a talc and/or chlorite rich ultramafic/mafic rock) in Valmalenco and Valchiavenna probably dates back to the Iron Age; in Valchiavenna it is documented with certainty since Roman times and the Middle Ages. The extraction and processing of soapstone peaked around the middle of the XVIII century, with a dozen quarries and about 300 workers involved, between Chiavenna and Piuro. A limited production of soapstone is still active in the municipalities of Piuro (talc-olivine-tremolite fels) and Chiesa in Valmalenco (chlorite schist), where in addition to the traditional cooking pots ("Lavecc"), there is a growing art work and gift items production. With the exception of two companies that have reached an industrial production level, the remaining 24 companies operating in Valmalenco are on an artisan level, and are grouped in the "Consorzio Artigiani Cavatori Valmalenco". The consortium, already engaged in the management of a permanent storage of explosives at the service of the quarries, promotes and subsidizes economically various initiatives aimed at the enhancement of stone products and the development of this craft. The consortium is a promoter of a cultural initiative aimed at the restoration of an underground quarry and the ancient paths of "Giovello", a historic site for the extraction and processing of serpentinite.

Two-stage fluid flow and element transfers in shear zones during collision burial-exhumation cycle: Insights from the Mont Blanc Crystalline Massif (Western Alps)

NASA Astrophysics Data System (ADS)

Rolland, Y.; Rossi, M.

2016-11-01

The Mont-Blanc Massif was intensely deformed during the Alpine orogenesis: in a first stage of prograde underthrusting at c. 30 Ma and in a second stage of uplift and exhumation at 22-11 Ma. Mid-crustal shear zones of 1 mm-50 m size, neighbouring episyenites (quartz-dissolved altered granite) and alpine veins, have localised intense fluid flow, which produced substantial changes in mineralogy and whole-rock geochemistry. Four main metamorphic zones are oriented parallel to the strike of the massif: (i) epidote, (ii) chlorite, (iii) actinolite-muscovite ± biotite and (iv) muscovite ± biotite. In addition, phlogopite-bearing shear zones occur in the chlorite zone, and calcite-bearing shear zones are locally found in the muscovite zone. The initial chemical composition of the granitic protolith is relatively constant at massif scale, which allows investigating compositional changes related to shear zone activity, and subsequent volume change and elements mobility. The variations of whole-rock composition and mineral chemistry in shear zones reflect variations in fluid/rock ratios and fluid's chemistry, which have produced specific mineral reactions. Estimated time-integrated fluid fluxes are of the order of 106 m3/m2. The mineral assemblages that crystallised upon these fluid-P-T conditions are responsible for specific major and trace element enrichments. The XFe (Fe/Fe + Mg) pattern of shear zone phyllosilicates and the δ13C pattern of vein calcite both show a bell-type pattern across the massif with high values on the massif rims and low values in the centre of the massif. These low XFe and δ13C values are explained by down temperature up-flow of a Fe-Mg-CO2-rich and silica-depleted fluid during stage 1, while the massif was underthrusting. These produced phlogopite, chlorite and actinolite precipitation and quartz hydrolysis, resulting in strong volume losses. In contrast, during stage 2 (uplift), substantial volume gains occurred on the massif rims due to the precipitation of quartz, epidote and muscovite from a local fluid hosted in the Helvetic cover. These two fluids advocate for the presence of an upper-crustal scaled fluid convection cell, with up-going fluids through the lower crust and likely down-going fluids in the 15 km upper crust.

Recycling of water, carbon, and sulfur during subduction of serpentinites: A stable isotope study of Cerro del Almirez, Spain

NASA Astrophysics Data System (ADS)

Alt, Jeffrey C.; Garrido, Carlos J.; Shanks, W. C.; Turchyn, Alexandra; Padrón-Navarta, José Alberto; López Sánchez-Vizcaíno, Vicente; Gómez Pugnaire, María Teresa; Marchesi, Claudio

2012-04-01

We use the concentrations and isotope compositions of water, carbon, and sulfur in serpentinites and their dehydration products to trace the cycling of volatiles during subduction. Antigorite serpentinites from the Cerro del Almirez complex, Spain, contain 9-12 wt.% H2O and 910 ± 730 ppm sulfur, and have bulk δ18O values of 8.6 ± 0.4‰, δD = - 54 ± 5‰, and δ34S = 5.0‰, consistent with serpentinization at temperatures of ~ 200 °C by seawater hydrothermal fluids in a seafloor setting. The serpentinites were dehydrated to chlorite-harzburgite (olivine + orthopyroxene + chlorite) at 700 °C and 1.6-1.9 GPa during subduction metamorphism, resulting in loss of water, and sulfur. The chlorite-harzburgites contain 5.7 ± 1.9 wt.% H2O, and have bulk δ18O = 8.0 ± 0.9‰, and δD = - 77 ± 11‰. The rocks contain 650 ± 620 ppm sulfur having δ34S = 1.2‰. Dehydration of serpentinite resulted in loss of 5 wt.% H2O having δ18O = 8-10‰ and δD = - 27 to - 65‰, and loss of 260 ppm sulfur as sulfate, having δ34S = 14.5‰. The contents and δ13C of total carbon in the two rock types overlap, with a broad trend of decreasing carbon contents and δ13C from ~ 1300 to 200 ppm and - 9.6 to - 20.2‰. This reflects mixing between reduced carbon in the rocks (210 ppm, δ13C ≈ - 26‰) and seawater-derived carbonate (δ13C ≈ - 1‰). Our results indicate: 1) Serpentinized oceanic peridotites carry significant amounts of isotopically fractionated water, carbon and sulfur into subduction zones; 2) Subduction of serpentinites to high P and T results in loss of water, and sulfur, which can induce melting and contribute to 18O, D, and 34S enrichments and oxidation of the sub-arc mantle wedge; and 3) Isotopically fractionated water, carbon, and sulfur in serpentinite dehydration products are recycled deeper into the mantle where they can contribute to isotope heterogeneities and may be significant for volatile budgets of the deep Earth.

Clay minerals trap hydrogen in the Earth's crust: Evidence from the Cigar Lake uranium deposit, Athabasca

NASA Astrophysics Data System (ADS)

Truche, Laurent; Joubert, Gilles; Dargent, Maxime; Martz, Pierre; Cathelineau, Michel; Rigaudier, Thomas; Quirt, David

2018-07-01

Hydrogen (H2)-rich fluids are observed in a wide variety of geologic settings including gas seeps in serpentinized ultramafic rocks, sub-seafloor hydrothermal vents, fracture networks in crystalline rocks from continental and oceanic crust, and volcanic gases. Natural hydrogen sources can sustain deep microbial ecosystems, induce abiotic hydrocarbons synthesis and trigger the formation of prebiotic organic compounds. However, due to its extreme mobility and small size, hydrogen is not easily trapped in the crust. If not rapidly consumed by redox reactions mediated by bacteria or suitable mineral catalysts it diffuses through the rocks and migrates toward the surface. Therefore, H2 is not supposed to accumulate in the crust. We challenge this view by demonstrating that significant amount of H2 may be adsorbed by clay minerals and remain trapped beneath the surface. Here, we report for the first time H2 content in clay-rich rocks, mainly composed of illite, chlorite, and kaolinite from the Cigar Lake uranium ore deposit (northern Saskatchewan, Canada). Thermal desorption measurements reveal that H2 is enriched up to 500 ppm (i.e. 0.25 mol kg-1 of rock) in these water-saturated rocks having a very low total organic content (<0.5 wt%). Such hydrogen uptake is comparable and even exceeds adsorbed methane capacities reported elsewhere for pure clay minerals or shales. Sudoite (Al-Mg di-trioctahedral chlorite) is probably the main mineral responsible for H2 adsorption in the present case. The presence of multiple binding sites in interlinked nanopores between crystal layers of illite-chlorite particles offers the ideal conditions for hydrogen sorption. We demonstrate that 4 to 17% of H2 produced by water radiolysis over the 1.4-Ga-lifetime of the Cigar Lake uranium ore deposit has been trapped in the surrounding clay alteration haloes. As a result, sorption processes on layered silicates must not be overlooked as they may exert an important control on the fate and mobility of H2 in the crust. Furthermore, the high capacity of clay minerals to sorb molecular hydrogen may also open up new opportunities for exploration of unexpected energy resources and for H2 storage based on geo-inspired materials.

Aqueous alteration revealed by diverse mineralogy at Amazonian-aged Lyot crater, Mars

NASA Astrophysics Data System (ADS)

Pan, L.; Ehlmann, B. L.

2016-12-01

Located close to the hemispheric dichotomy, Lyot crater is the largest (with diameter 220 km) and deepest impact crater in the northern lowlands of Mars. The impact event could have released substantial amount of volatiles and strongly influenced the evolution of Amazonian Mars climate [1]. Previous works have shown that the impact event probably induced overland flow that formed the channels north of Lyot [2] and within the crater, kilometer-long valleys have formed in micro-environments that post-date the impact [3]. These features suggest that groundwater may have been mobilized in the subsurface, and there was melting of ice-rich deposits after the impact event. In a recent mineralogy survey [4], diverse hydrated minerals in and around Lyot crater have been revealed by data acquired from Compact Reconnaissance Imaging Spectrometer for Mars (CRISM). The concentration of hydrated minerals in this region is much greater than average northern plains, suggesting substantial aqueous alteration directly associated to the Lyot impact or in the regional stratigraphy. We have found 7 Fe/Mg phyllosilicate detections, likely smectite or mixed-layer smectite-chlorite, in the central ring region; 10 chlorite/prehnite detections (identified with a typical 2.35 µm absorption, in which 2 have an additional 1.48 µm absorption that matches prehnite, confirming [5]) in the central ring, crater floor, outer rim, and ejecta blanket; and 9 locations with absorptions at 2.21 µm with/without the coexistence with the 2.35 µm feature, which can be explained by illite/muscovite or a mixture of hydrated silica and chlorite/prehnite. The unit with 2.21-µm absorptions is often associated with the smooth mantling deposit, superposed on the valleys within the crater and on the crater rim. Further morphological analysis over these units with distinct mineralogy will shed light on the aqueous activity that formed these minerals. Combined with geological map of the region, we will establish the timeline of aqueous activities associated with the impact and provide insights into the climatic influence of Lyot impact in the Amazonian age. [1] Toon et al. (2010) Ann. Rev Earth Plan. Sci 38 [2] Harrison et al. (2010) GRL 37(21) [3] Dickson et al. (2010) GRL 36(8) [4] Pan, Ehlmann, Carter, Ernst, JGR Planets, submitted [5] Carter et al., (2010) Science.

Sequence-stratigraphic controls on sandstone diagenesis: An example from the Williams Fork formation, Piceance Basin, Colorado

NASA Astrophysics Data System (ADS)

Aboktef, Adel

This study documents the distribution of diagenetic alterations in Williams Fork fluvial sandstones, assess sequence stratigraphic controls on diagenetic features, and addresses diagenetic impacts on porosity. Petrographic point counts of 220 thin sections from six wells forms the database. The near absence of potassium feldspar and volcanic rock fragments in the lower Williams Fork interval and increasing plagioclase content upward represent changes in sediment provenance rather than stratigraphic variability in diagenesis. The lower Williams Fork sands are from sedimentary sources whereas middle and upper Williams Fork sands include input from magmatic arcs and basement uplifts. Compaction, early and late cementation, dissolution, and replacement by calcite or clay minerals combined to alter Williams Fork sandstones. Infiltration of clays occurred prior to any burial. Chlorite, quartz, non-ferroan calcite, compaction and dissolution features, and kaolinite formed during eo-diagenesis at <70°C. More quartz, compaction and dissolution features, plus albite, illite, mixed-layer illite/smectite, ferroan calcite, and dolomite formed in the meso-diagenetic realm (>70°C). Four of these features show spatial variability with respect to systems tracts. Infiltrated clays are concentrated in lowstand systems tracts (LST) and highstand systems tracts (HST) because accommodation space rose slow or fell during deposition of those sands, which led to prolonged sand body exposure on floodplain and ample opportunities for downward percolation of mud during flood events. Concentration of pseudomatrix (mud intraclasts) in HST and LST deposits resulted from floodplain erosion when base-level fell with decreasing accommodation space. Authigenic chlorite formed in the HST and transgressive systems tracts (TST) of the upper half of the Williams Fork Formation because volcanic clasts are abundant in that interval. Quartz overgrowths are more likely to exceed 7% in TST deposits for reasons that are unknown. High total clay content (infiltrated, grain coatings, pseudomatrix) does inhibit quartz overgrowths in all systems tracts. Williams Fork sandstones form low-permeability tight-gas reservoirs. Primary porosity was almost entirely destroyed by compaction and cementation. Reservoir rock resulted from one of two pathways. Eogenetic authigenic chlorite and/or calcite inhibited quartz cementation, minimized compaction and protected some primary porosity. Alternately, dissolution of framework grains or cements created secondary porosity. The later pathway tends to be the more dominant.

Genesis of the Abu Marawat gold deposit, central Eastern Desert of Egypt

NASA Astrophysics Data System (ADS)

Zoheir, Basem A.; Akawy, Ahmed

2010-06-01

Gold mineralisation at the Abu Marawat mine, central Eastern Desert of Egypt, is related to a system of massive and sheared, milky quartz veins cutting a sequence of Neoproterozoic island arc metavolcanic/volcaniclastic rocks and related banded iron formation (BIF). Sulphide-bearing quartz veins and related hydrothermal breccia bodies display a range of textures including sheared, boudinaged and recrystallised quartz, open space filling and microbreccia. These variable textures imply a complex history of crack-seal mechanism characterising the relation between mineral deposition and a major N-S-trending shear zone, during a late brittle-ductile deformation event which affected the area at about 550 Ma. Gold-base metal mineralisation is associated with brecciation and fracturing of the iron ore bands, close to silicified shears and related quartz veins. The auriferous quartz lodes are characterised by the occurrence of visible pyrite-chalcopyrite ± pyrrhotite ± sphalerite ± galena mineralisation. Gold is refractory in pyrite and chalcopyrite, but rare visible gold/electrum and telluride specks were observed in a few samples. Hydrothermal alteration includes pervasive silicification, pyritisation, sericitisation, carbonatisation confined to a delicate set of veins and altered shears, and a more widespread propylitic alteration assemblage (quartz + chlorite + pyrite + calcite ± epidote). Fluid inclusion petrography and microthermometric studies suggest heterogeneous trapping of a low-salinity (1.4-6.7 wt.% eq. NaCl) aqueous solution and a carbonic fluid. Evidence for fluid immiscibility during ore formation includes variable liquid/vapour ratios in inclusions along individual trails and bulk inclusion homogenisation into liquid and occasionally to vapour at comparable temperatures. The trapping conditions of intragranular aqueous-carbonic inclusions approximate 264-378 °C at 700-1300 bar. Similar temperature estimates have been obtained from Al-in-chlorite geothermometry of chlorite associated with sulphides in the mineralised quartz veins. Fracturing enhanced fluid circulation through the wallrock and related BIF, allowing reaction of the S-bearing ore fluid with iron oxides. This caused pyrite formation and concomitant Au precipitation, enhanced by fluid immiscibility as H 2S partitioned preferentially into the carbonic phase. The ore fluids may have originated from granitoid intrusions (likely the post-Hammamat felsites, whereas gold and base metals might have been leached from the Abu Marawat basic metavolcanics.

Metabasalts from the Mid-Atlantic Ridge: new insights into hydrothermal systems in slow-spreading crust

NASA Astrophysics Data System (ADS)

Gillis, Kathryn M.; Thompson, Geoffrey

1993-12-01

An extensive suite of hydrothermally altered rocks were recovered by Alvin and dredging along the MARK [Mid-Atlantic Ridge, south of the Kane Fracture Zone (23 24°N)] where detachment faulting has provided a window into the crustal component of hydrothermal systems. Rocks of basaltic composition are altered to two assemblages with these characteristics: (i) type I: albitic plagioclase (An02 10)+mixed-layer smectite/chlorite or chlorite±actinolite±quartz±sphene, <10% of the clinopyroxene is altered, and there is no trace metal mobility; (ii) type II: plagioclase (An10 30)+amphibole (actinolite-magnesio-hornblende) +chlorite+sphene, >20% of the clinopyroxene is altered, and Cu and Zn are leached. The geochemical signature of these alteration types reflects the relative proportion and composition of secondary minerals, and the degree of alteration of primary phases, and does not show simple predictive relationships. Element mobilities indicate that both alteration types formed at low water/rock ratios. The MARK assemblages are typical of the greenschist and transition to the amphibolite facies, and represent two distinct, albeit overlapping, temperature regimes: type I-180 to 300°C and type II-250 to 450°C. By analogy with DSDP/ODP Hole 504B and many ophiolites, the MARK metabasalts were altered within the downwelling limb of a hydrothermal cell and type I and II samples formed in the upper and lower portions of the sheeted like complex, respectively. Episodic magmatic and hydrothermal events at slow-spreading ridges suggest that these observed mineral assemblages represent the cumulative effects of more than one hydrothermal event. Groundmass and vein assemblages in the MARK metabasalts indicate either that alteration conditions did not change during successive hydrothermal events or that these assemblages record only the highest temperature event. Lack of retrograde reactions or overprinting of lower temperature assemblages (e.g., zeolites) suggests that there is a continuum in alteration conditions while crustal segments remain in the ridge axis environment. The type II samples may be representative of the reaction zone where compositions of hydrothermal fluids actively venting at the seafloor today become fixed. This prediction necessitates interaction between hydrothermal fluids and intersertal glass and/or mafic phases, in addition to plagioclase, in order to produce the observed range in vented fluid pH.

Hydrothermal alteration of felsic volcanic rocks at the Helen Siderite Deposit, Wawa, Ontario

DOE Office of Scientific and Technical Information (OSTI.GOV)

Morton, R.L.; Nebel, M.L.

1984-09-01

Felsic lavas and pyroclastic rocks, underlying the Archean Helen iron-formation, have been variably altered by hydrothermal solutions which, when discharged onto the sea floor, formed the Helen siderite deposit. Within the footwall volcanic sequence five chemically and mineralogically distinct alteration types have been defined: least altered, sericite, chlorite chloritoid, and ankerite. Based on mineralogy and chemistry of the altered rocks and on the geometry of the alteration zones, an alteration model is proposed.

Mineralogical constraints on the paleoenvironments of the Ediacaran Doushantuo Formation

PubMed Central

Bristow, Thomas F.; Kennedy, Martin J.; Derkowski, Arkadiusz; Droser, Mary L.; Jiang, Ganqing; Creaser, Robert A.

2009-01-01

Assemblages of clay minerals are routinely used as proxies for paleoclimatic change and paleoenvironmental conditions in Phanerozoic rocks. However, this tool is rarely applied in older sedimentary units. In this paper, the clay mineralogy of the Doushantuo Formation in South China is documented, providing constraints on depositional conditions of the Ediacaran Yangtze platform that host the earliest animal fossils in the geological record. In multiple sections from the Yangtze Gorges area, trioctahedral smectite (saponite) and its diagenetic products (mixed-layer chlorite/smectite, corrensite, and chlorite) are the dominant clays through the lower 80 m of the formation and constitute up to 30 wt% of the bulk rock. Saponite is interpreted as an in situ early diagenetic phase that formed in alkaline conditions (pH ≥ 9). The absence of saponite in stratigraphically equivalent basin sections, 200–400 km to the south, indicates that alkaline conditions were localized in a nonmarine basin near the Yangtze Gorges region. This interpretation is consistent with crustal abundances of redox-sensitive trace elements in saponitic mudstones deposited under anoxic conditions, as well as a 10‰ difference in the carbon isotope record between Yangtze Gorges and basin sections. Our findings suggest that nonmarine environments may have been hospitable for the fauna preserved in the Yangtze Gorges, which includes the oldest examples of animal embryo fossils and acanthomorphic acritarchs. PMID:19666508

Environmental implication of subaqueous lava flows from a continental Large Igneous Province: Examples from the Moroccan Central Atlantic Magmatic Province (CAMP)

NASA Astrophysics Data System (ADS)

El Ghilani, S.; Youbi, N.; Madeira, J.; Chellai, E. H.; López-Galindo, A.; Martins, L.; Mata, J.

2017-03-01

The Late Triassic-Early Jurassic volcanic sequence of the Central Atlantic Magmatic Province (CAMP) of Morocco is classically subdivided into four stratigraphic units: the Lower, Middle, Upper and Recurrent Formations separated by intercalated sediments deposited during short hiatuses in volcanic activity. Although corresponding to a Large Igneous Province formed in continental environment, it contains subaqueous lava flows, including dominant pillowed flows but also occasional sheet flows. We present a study of the morphology, structure and morphometry of subaqueous lava flows from three sections located at the Marrakech High-Atlas (regions of Aït-Ourir, Jbel Imzar and Oued Lhar-Herissane), as well as an analysis of the sediments, in order to characterize them and to understand their environmental meaning. The analysis of clays by the diffraction method X-ray revealed the presence of illite, mica, phengite, céladonite, talc and small amounts of quartz, hematite, calcite and feldspar, as well as two pairs of interbedded irregular (chlorite Smectite/chlorite-Mica). Fibrous minerals such as sepiolite and palygorskite were not detected. The peperite of Herissane region (Central High Atlas) provided an excellent overview on the factors favoring the magma-sediment interaction. These are the products of a mixture of unconsolidated or poorly consolidated sediments, low permeability with a low viscosity magma. The attempt of dating palynology proved unfortunately without results.

Petrography and character of the bedrock surface beneath western Cape Cod, Massachusetts

USGS Publications Warehouse

Hallett, B.W.; Poppe, L.J.; Brand, S.G.

2004-01-01

Cores collected during recent drilling in western Cape Cod, Massachusetts provide insight into the topography and petrology of the underlying bedrock. 62 drill sites spread over a ???140 km2 study area produced cores of granitoids (31), orthogneisses (20), basalts/diabases (4), amphibolites (3), felsic mylonites (2), and dolomitic rock (2). Granitoid cores range in composition from granite to tonalite to quartz diorite, but are dominated by single-mica granites. Alteration is common in nearly all cores examined in this study, and is evidenced by the secondary growth of chlorite and epidote. The granitoids resemble rocks of the Dedham and Fall River terranes (Wones and Goldsmith 1991). Gneisses from the study area generally contain the mineral assemblage hornblende+plagioclase+quartz+biotite+epidote??chlorite?? sphene??K-feldspar??sericite+oxides. Based on mineral assemblages, we estimate peak metamorphic grade to be of lower amphibolite facies. X-ray powder diffraction of unmetamorphosed dolomitic cores shows presence of layered silicates (clays), plagioclase, and possible magnesite. Contours of the bedrock surface show locally irregular topography suggesting erosion by glacial scour. The distribution of lithologies suggests a possible continuation of the New Bedford gneissic terrane that outcrops 25 km to the west. Dolomitic rocks may represent a lithified fault gouge material at the eastern edge of the gneissic zone. Basalts/diabases are interpreted to be post-metamorphic dikes of Late Paleozoic age, or possibly associated with Mesozoic rifting.

Chlorate reductase is cotranscribed with cytochrome c and other downstream genes in the gene cluster for chlorate respiration of Ideonella dechloratans.

PubMed

Hellberg Lindqvist, Miriam; Nilsson, Thomas; Sundin, Pontus; Rova, Maria

2015-03-01

The chlorate-respiring bacterium Ideonella dechloratans is a facultative anaerobe that can use both oxygen and chlorate as terminal electron acceptors. The genes for the enzymes chlorate reductase (clrABDC) and chlorite dismutase, necessary for chlorate metabolism and probably acquired by lateral gene transfer, are located in a gene cluster that also includes other genes potentially important for chlorate metabolism. Among those are a gene for cytochrome c (cyc) whose gene product may serve as an electron carrier during chlorate reduction, a cofactor biosynthesis gene (mobB) and a predicted transcriptional regulator (arsR). Only chlorate reductase and chlorite dismutase have been shown to be expressed in vivo. Here, we report the in vivo production of a single polycistronic transcript covering eight open reading frames including clrABDC, cyc, mobB and arsR. Transcription levels of the cyc and clrA genes were compared to each other by the use of qRT-PCR in RNA preparations from cells grown under aerobic or chlorate reducing anaerobic conditions. The two genes showed the same mRNA levels under both growth regimes, indicating that no transcription termination occurs between them. Higher transcription levels were observed at growth without external oxygen supply. Implications for electron pathway integration following lateral gene transfer are discussed. © FEMS 2015. All rights reserved. For permissions, please e-mail: journals.permissions@oup.com.

[Effects of Long-term Implementation of the Flow-Sediment Regulation Scheme on Grain and Clay Compositions of Inshore Sediments in the Yellow River Estuary].

PubMed

Wang, Miao-miao; Sun, Zhi-gao; Lu, Xiao-ning; Wang, Wei; Wang, Chuan-yuan

2015-04-01

Based on the laser particle size and X-ray diffraction (XRD) analysis, 28 sediment samples collected from the inshore region of the Yellow River estuary in October 2013 were determined to discuss the influence of long-term implementation of the flow-sediment regulation scheme (FSRS, initiated in 2002) on the distributions of grain size and clay components (smectite, illite, kaolinite and chlorite) in sediments. Results showed that, after the FSRS was implemented for more than 10 years, although the proportion of sand in inshore sediments of the Yellow River estuary was higher (average value, 23.5%) than those in sediments of the Bohai Sea and the Yellow River, silt was predominated (average value, 59.1%) and clay components were relatively low (average value, 17.4%). The clay components in sediments of the inshore region in the Yellow River estuary were close with those in the Yellow River. The situation was greatly changed due to the implementation of FSRS since 2002, and the clay components were in the order of illite > smectite > chlorite > kaolinite. This study also indicated that, compared to large-scale investigation in Bohai Sea, the local study on the inshore region of the Yellow River estuary was more favorable for revealing the effects of long-term implementation of the FSRS on sedimentation environment of the Yellow River estuary.

Clay mineralogical and geochemical proxies of the East Asian summer monsoon evolution in the South China Sea during Late Quaternary

PubMed Central

Chen, Quan; Liu, Zhifei; Kissel, Catherine

2017-01-01

The East Asian summer monsoon controls the climatic regime of an extended region through temperature and precipitation changes. As the East Asian summer monsoon is primarily driven by the northern hemisphere summer insolation, such meteorological variables are expected to significantly change on the orbital timescale, influencing the composition of terrestrial sediments in terms of both mineralogy and geochemistry. Here we present clay mineralogy and major element composition of Core MD12-3432 retrieved from the northern South China Sea, and we investigate their relationship with the East Asian summer monsoon evolution over the last 400 ka. The variability of smectite/(illite + chlorite) ratio presents a predominant precession periodicity, synchronous with the northern hemisphere summer insolation changes and therefore with that of the East Asian summer monsoon. Variations in K2O/Al2O3 are characterized by eccentricity cycles, increasing during interglacials when the East Asian summer monsoon is enhanced. Based on the knowledge of sediment provenances, we suggest that these two proxies in the South China Sea are linked to the East Asian summer monsoon evolution with different mechanisms, which are (1) contemporaneous chemical weathering intensity in Luzon for smectite/(illite + chlorite) ratio and (2) river denudation intensity for K2O/Al2O3 ratio of bulk sediment. PMID:28176842

Clay mineralogical and geochemical proxies of the East Asian summer monsoon evolution in the South China Sea during Late Quaternary.

PubMed

Chen, Quan; Liu, Zhifei; Kissel, Catherine

2017-02-08

The East Asian summer monsoon controls the climatic regime of an extended region through temperature and precipitation changes. As the East Asian summer monsoon is primarily driven by the northern hemisphere summer insolation, such meteorological variables are expected to significantly change on the orbital timescale, influencing the composition of terrestrial sediments in terms of both mineralogy and geochemistry. Here we present clay mineralogy and major element composition of Core MD12-3432 retrieved from the northern South China Sea, and we investigate their relationship with the East Asian summer monsoon evolution over the last 400 ka. The variability of smectite/(illite + chlorite) ratio presents a predominant precession periodicity, synchronous with the northern hemisphere summer insolation changes and therefore with that of the East Asian summer monsoon. Variations in K 2 O/Al 2 O 3 are characterized by eccentricity cycles, increasing during interglacials when the East Asian summer monsoon is enhanced. Based on the knowledge of sediment provenances, we suggest that these two proxies in the South China Sea are linked to the East Asian summer monsoon evolution with different mechanisms, which are (1) contemporaneous chemical weathering intensity in Luzon for smectite/(illite + chlorite) ratio and (2) river denudation intensity for K 2 O/Al 2 O 3 ratio of bulk sediment.

Nucleation and growth of strike slip faults in granite.

USGS Publications Warehouse

Segall, P.; Pollard, D.P.

1983-01-01

Fractures within granodiorite of the central Sierra Nevada, California, were studied to elucidate the mechanics of faulting in crystalline rocks, with emphasis on the nucleation of new fault surfaces and their subsequent propagation and growth. Within the study area the fractures form a single, subparallel array which strikes N50o-70oE and dips steeply to the S. Some of these fractures are identified as joints because displacements across the fracture surfaces exhibit dilation but no slip. The joints are filled with undeformed minerals, including epidote and chlorite. Other fractures are identified as small faults because they display left-lateral strike slip separations of up to 2m. Slickensides, developed on fault surfaces, plunge 0o-20o to the E. The faults occur parallel to, and in the same outcrop with, the joints. The faults are filled with epidote, chlorite, and quartz, which exhibit textural evidence of shear deformation. These observations indicate that the strike slip faults nucleated on earlier formed, mineral filled joints. Secondary, dilational fractures propagated from near the ends of some small faults contemporaneously with the left-lateral slip on the faults. These fractures trend 25o+ or -10o from the fault planes, parallel to the direction of inferred local maximum compressive stress. The faults did not propagate into intact rock in their own planes as shear fractures. -from Authors

Effects of water, sodium hypochlorite, peroxyacetic acid, and acidified sodium chlorite on in-shell hazelnuts inoculated with Salmonella enterica serovar Panama.

PubMed

Weller, Lisa D; Daeschel, Mark A; Durham, Catherine A; Morrissey, Michael T

2013-12-01

Recent foodborne disease outbreaks involving minimally processed tree nuts have generated a need for improved sanitation procedures. Chemical sprays and dips have shown promise for reducing pathogens on fresh produce, but little research has been conducted for in-shell hazelnuts. This study analyzed the effectiveness of 3 chemical sanitizers for reducing Salmonella on in-shell hazelnuts. Treatments of water, sodium hypochlorite (NaOCl; 25 and 50 ppm), peroxyacetic acid (PAA; 80 and 120 ppm), and acidified sodium chlorite (ASC; 450, 830, and 1013 ppm) were sprayed onto hazelnut samples inoculated with Salmonella enterica serovar Panama. Hazelnut samples were immersed in liquid cultures of S. Panama for 24 h, air-dried, and then sprayed with water and chemical treatments. Inoculation achieved S. Panama populations of approximately 8.04 log CFU/hazelnut. Surviving S. panama populations were evaluated using a nonselective medium (tryptic soy agar), incubated 3 h, and then overlaid with selective media (xylose lysine deoxycholate agar). All of the chemical treatments significantly reduced S. Panama populations (P ≤ 0.0001). The most effective concentrations of ASC, PAA, and NaOCl treatments reduced populations by 2.65, 1.46, and 0.66 log units, respectively. ASC showed the greatest potential for use as a postharvest sanitation treatment. © 2013 Institute of Food Technologists®

Direct injection ion chromatography for the control of chlorinated drinking water: simultaneous estimation of nine haloacetic acids and quantitation of bromate, chlorite and chlorate along with the major inorganic anions.

PubMed

Garcia-Villanova, Rafael J; Raposo Funcia, César; Oliveira Dantas Leite, M Vilani; Toruño Fonseca, Ivania M; Espinosa Nieto, Miguel; Espuelas India, Javier

2014-09-01

Most methods for the analysis of haloacetic acids published in recent years are based on ion chromatography with direct injection, employing a gradient elution with potassium hydroxide (KOH). This work reports the exploration of an alternative eluent, a buffer of sodium carbonate/sodium hydrogen carbonate, aimed at the simultaneous analysis of nine haloacetic acids along with bromate, chlorite and chlorate. The alternative of both a less alkaline eluent and a lower temperature of operation may prevent the partial decomposition of some of the haloacetic acids during the analytical process, especially the more vulnerable brominated ones. Gradient elution at temperature of 7 °C yielded the best results, with an acceptable separation of 17 analytes (which includes the major natural inorganic anions) and a good linearity. Precision ranges from 0.3 to 23.4 (% V.C.), and detection limits are within units of μg L⁻¹, except for tribromoacetic acid - somewhat high in comparison with those of the official methods. Nonetheless, with the basic instrumentation setup herein described, this method may be suitable for monitoring when the drinking water treatments are to be optimized. This is especially interesting for small communities or for developing/developed countries in which regulations on disinfection by-products others than trihalomethanes are being addressed.

Acidified sodium chlorite optimisation assessment to improve quality of fresh-cut tatsoi baby leaves.

PubMed

Tomás-Callejas, Alejandro; López-Velasco, Gabriela; Artés, Francisco; Artés-Hernández, Francisco

2012-03-15

The fresh-cut industry commonly uses sodium hypochlorite (NaClO) for disinfection. However, there are certain problems related to its use, and acidified sodium chlorite (ASC) could be an alternative sanitiser to replace it. There is limited research evaluating the effect of ASC on the overall quality of fresh-cut produce, especially sensory quality. In this study the decontamination efficacy and quality attribute effects of ASC on fresh-cut tatsoi after application and during storage were investigated. Tatsoi baby leaves were minimally processed at 8 °C and stored under passive modified atmosphere packaging for up to 11 days at 5 and 10 °C. Low to moderate doses of ASC (100-500 mg L⁻¹) showed an initial antimicrobial efficacy on natural microflora and Escherichia coli as effective as that of NaClO. Regarding contact time, ASC was effective in reducting the E. coli population during the first 30 s of washing, and an increase in contact time did not improve the antimicrobial effect. Sensory quality attributes were well kept for up to 11 days at 5 °C but for only 5 days at the abusive temperature of 10 °C. ASC provides an alternative sanitising technique to NaClO for maintaining the quality and safety of fresh-cut tatsoi baby leaves for up to 11 days at 5 °C. Copyright © 2011 Society of Chemical Industry.

Water incorporation in NAMs after antigorite and chlorite dehydration reactions

NASA Astrophysics Data System (ADS)

Padrón-Navarta, José Alberto; Hermann, Jörg

2014-05-01

Subduction zones play a fundamental role in the deep water cycle making the Earth unique among other terrestrial planets. Water is incorporated into hydrous minerals during seafloor alteration of the oceanic lithosphere. During subduction of the oceanic lithosphere, dehydration of these hydrous minerals produces a fluid phase. A part of this fluid phase will be recycled back to the Earth's surface through hydrothermal aqueous fluids or through hydrous arc magmas, whereas another part of the water will be transported to the deep mantle by Nominally Anhydrous Minerals (NAMs) such as olivine, pyroxene and garnet. The partitioning of water between these two processes is crucial for our understanding of the mantle-scale water recycling in the Earth. This can be investigated experimentally under water-saturated conditions because this situation is met during dehydration reactions. However relatively low temperature conditions for such reactions make challenging these experiments. An alternative can be found in the natural record. The Alpine Betic-Rif orogen together with Central and Western Alps offer an invaluable diversity of ultramafic lenses that record a significant range of pressure-temperature and cooling rates. Hence these samples portray an excellent data set of 24 samples to survey the transfer of fluids from hydrous phases (brucite, antigorite and chlorite) to NAMs (olivine, orthopyroxene, clinopyroxene and garnet). Well-studied samples from these localities have been selected for water measurement using FTIR spectroscopy. The selected suite comprises the following high-pressure peridotite outcrops: Malenco serpentinite, Cerro del Almirez (1.6-1.9 GPa and 680-710ºC), Alpe Arami (3.2 GPa and 840ºC), Cima di Gagnone (3.0 GPa and 750-800ºC) and Alpe Albion (0.6 GPa and 730ºC). The infrared signature of olivine in all localities contains water (hydroxyl groups) associated to intrinsic defects (mostly point defects related to Ti4+) and extrinsic submicroscopic hydrous lamellae (titanoclinohumite). In the following only water contents related to intrinsic defects are reported. At low temperature (400-450 ºC) the spectra of olivine coexisting with antigorite are dominated by OH associated to silica-vacancies and contains 12-20 wt. ppm H2O (using site-specific infrared OH absorption coefficients from [1]). Olivine in equilibrium with orthopyroxene and chlorite formed after the antigorite breakdown (650-700 ºC) at high pressure (1.6-1.9 GPa) from Cerro del Almirez contains 14-17 ppm and is associated to Ti4+ and abundant extrinsic defects. Surprisingly the associated orthopyroxene is nearly dry (1-3 wt. ppm) resulting in D[opx/ol] 1. After chlorite breakdown (750-800ºC) olivine contains 21-68 wt. ppm H2O. In summary there is a systematic correlation between PT conditions and water content in olivine and orthopyroxene. The dependence is however different for both resulting in significant changes in the water partition coefficient. This dataset represents a first step in the quantification of the water budget in the slab and in the mantle wedge of NAMs coexisting with hydrous phases and after their breakdown. [1] Kovacs, I., O'Neill, H.S.C., Hermann, J., Hauri, E.H., 2010. Site-specific infrared O-H absorption coefficients for water substitution into olivine. Am. Miner. 95, 292-299.

The blueschits from the Kopina Mt., West Sudetes, Poland - what do they tell us about accretion of the Variscides?

NASA Astrophysics Data System (ADS)

Majka, Jarosław; Mazur, Stanisław; Kośmińska, Karolina; Dudek, Krzysztof

2015-04-01

Blueschists are tracers of sutures, thus marking fossil subduction zones at convergent plate boundaries and providing important constraints on plate tectonic reconstructions. Their occurrences are scarce in the Variscan belt owing to a strong collisional overprint but just because of that each locality deserves particular attention. The Variscan blueschists must have formed during the early stage of the Variscan Orogeny and may represent a vestige of missing marginal basins fringing the Rheic Ocean at the onset of subduction. The studied rocks from the Kopina Mt. consist mainly of garnet, glaucophane, clinozoisite-epidote, chlorite-I, titanite, hematite and quartz. The original high-pressure assemblage is overprinted by later, lower pressure paragenesis, which comprises mostly Ca-amphiboles, chlorite-II, albite and K-feldspar. The latter occurs in polymineral inclusions in other phases together with albite and chlorite that are interpreted as phengite breakdown products. Garnet shows chemical compositional variation from Alm54Prp3Grs30Sps13 in the cores to Alm66Prp4Grs29Sps1 in the rims. The almandine zoning is bowl-shaped, whereas spessartine profiles show bell-shaped trends. The grossular and pyrope contents are generally constant throughout the grain. Rather gradual changes in the chemical zoning suggest a progressive, one-step garnet growth pattern. Glaucophane, although commonly well preserved, in some cases disintegrates to the albite-chlorite assemblage. The pressure-temperature (P-T) conditions were estimated using the phase equilibrium modelling in the NCKFMMnASHTO system using the PerpleX software. The compositional isopleths cross cut in the stability field of Grt+Gln+Ep+Chl+Pheng+Ttn+Hem+Q. P-T estimates indicate that the peak conditions occur at c. 14-17 kbar and 470-500°C, which corresponds to quite a low geothermal gradient in the range of 8-10°C/km. The P-T conditions estimated lie on a low temperature geotherm that is typical for a relatively cool subduction of the oceanic crust. Therefore, the origin of the studied rocks dates back to the time preceding accretion of the eastern Variscides and defines one of the key tectonic boundaries in the Bohemian Massif. A mechanism for syn-collisional emplacement and exhumation of the Kopina blueschists can be tentatively explained through activation of the double subduction system operating towards the east. First subduction commenced already in the Early Devonian and operated beneath an island arc located in proximity to the Saxothuringian margin, within the Rheic Ocean. After the mid-Devonian exhumation of the Central Sudetes allochthon, another subduction system was initiated along the eastern margin of the Rheic Ocean, beneath the Brunia microplate. Subducted oceanic crust of the Rheic Ocean (including the Kopina Mt. blueschists) reached peak metamorphic conditions in the Late Devonian, the event pronounced by a continental arc volcanism along the Brunian margin. Exhumation of the subducted oceanic crust was accommodated by the slab roll-back, which is inferred from the bimodal age and spatial distribution of the volcanic activity within the Brunian active margin. Shortly after the Kopina Mt. blueschists exhumation this eastern subduction system became probably inactive. In contrast, the western one involving the Saxothuringian margin was still operating leading to the subsequent collision with Brunia in the Early Carboniferous that produced a widespread high temperature overprint mostly wiping up the earlier metamorphic history.

Interstellar dust spectra between 2.5 and 3.3 microns - A search for hydrated silicates

NASA Technical Reports Server (NTRS)

Knacke, R. F.; Mccorkle, S.; Puetter, R. C.; Erickson, E.

1985-01-01

Spectra in the 2.5-3.3 micron wavelength region of VI Cyg 12, AFGL 2205, and AFGL 2885 were obtained in a search for bound water, hydroxyl groups, and hydrated minerals in interstellar dust. No new absorption bands were found. Comparison of expected strengths of bands of serpentine and chlorite-like minerals with the data suggests that less than 25 percent and 50 percent, respectively, of the silicate in the grains is composed of these materials.

Synthesis of the 1-Monoester of 2-Ketoalkanedioic Acids, e.g., Octyl α-Ketoglutarate

PubMed Central

Jung, Michael E.; Deng, Gang

2012-01-01

Oxidative cleavage of cycloalkene-1-carboxylates, made from the corresponding carboxylic acids, and subsequent oxidation of the resulting ketoaldehyde afforded the important 1-monoesters of 2-ketoalkanedioic acids. Thus ozonolysis of octyl cyclobutene-1-carboxylate followed by sodium chlorite oxidation afforded the 1-monooctyl 2-ketoglutarate. This is a cell-permeable prodrug form of α-ketoglutarate, an important intermediate in the tricarboxylic acid (TCA, Krebs) cycle and a promising therapeutic agent in its own right. PMID:23163977

Density fingering in spatially modulated Hele-Shaw cells

DOE Office of Scientific and Technical Information (OSTI.GOV)

Toth, Tamara; Horvath, Dezso; Toth, Agota

Density fingering of the chlorite-tetrathionate reaction has been studied experimentally in a periodically heterogeneous Hele-Shaw cell where the heterogeneity is introduced in the form of spatial modulation of gap width along the front. Depending on the spatial wavelength, gap width, and chemical composition, three types of cellular structures have been observed. The initial evolution is characterized by dispersion curves, while the long time behavior is described by the change in the autocorrelation function of the front profile and in the mixing length of the patterns.

Hydrothermal karst and associated breccias in Neoproterozoic limestone from the Barker-Villa Cacique area (Tandilia belt), Argentina

NASA Astrophysics Data System (ADS)

Dristas, Jorge A.; Martínez, Juan C.; van den Kerkhof, Alfons M.; Massonne, Hans-Joachim; Theye, Thomas; Frisicale, María C.; Gregori, Daniel A.

2017-07-01

In the Barker-Villa Cacique area (Tandilia belt), remarkable megabreccias, limestone breccias and phosphate-bearing breccias hosted in black limestone and along the contact with the upper section of the sedimentary succession are exposed. These rocks are the result of extensive hydrothermal alteration of the original micritic limestone and other fine-grained clastic sediments. Typical alteration minerals are sericite, chlorite, interstratified chlorite/K-white mica, kaolinite, dickite, pyrite, chalcopyrite, goethite, quartz, calcite, Fe-calcite, dolomite, ankerite, fluor-apatite, barite and aluminium-phosphate-sulfate (APS) minerals. Quartz and calcite cements from hydraulic breccias in the limestone contain low-salinity aqueous fluid inclusions. Corresponding homogenization temperatures display 200-220 °C and 110-140 °C in hydrothermal quartz, and 130-150 °C in late calcite cement. Carbon and oxygen stable isotope analyses of carbonates from the Loma Negra quarry (LNQ) support the major role of hydrothermal activity. A significant difference was found between δ18Ocar values from unaltered micritic limestone (ca. 23.8‰ SMOW) and secondary calcite (ca. 18.5‰ SMOW). The lower δ18Ocar values are interpreted as a result of calcite precipitation from hot hydrothermal fluids. At a late stage, the hydrothermal fluid containing H2S mixed with descending and oxidizing meteoric waters. Circulation of the ensuing acid fluids resulted in the partly dissolution and collapse brecciation of the Loma Negra Formation. The hydrothermal stage can be tentatively dated ca. 590-620 Ma corresponding to the Brasiliano orogeny.

Alteration Minerals Extraction Using Airborne Hyperspectral Data Casi and Sasi in Wuyi Metallogenic Belt, China

NASA Astrophysics Data System (ADS)

Huang, Z.; Zheng, J.

2018-04-01

Hydrothermal alteration is an important content in the study of epithermal deposit, and its deep part is often accompanied by porphyry mineralization. The objective of research is to mapping the alteration minerals for mineral exploration using mixture tuned matched filtering (MTMF) approach based on airborne hyperspectral data CASI and SASI in Wuyi metallogenic belt, China, which has complex geological structure and excellent mineralization conditions and high regional forest coverage rate. Gold mineralization is closely related to the Yanshan period epithermal intrusive rocks, and often exists in external contact zone of allgovite, monzomite porphyrite, granite porphyry, quarz porphyry, et al.. The main mineral alteration types include silicification (quartz), sericitization (sericite, illite), pyritization (pyrite), chloritization (chlorite), and partial calcitization (calcite). The alteration minerals extraction based on integrated CASI_SASI reflectance data were processed by MTMF algorithm with the input imagery which was pre-processed by MNF and the input endmember spectra measured by SVC spectrometer to performs MF and add an infeasibility image. The MTMF results provide an estimate to mineral subpixel fractions leading to the abundances of alteration minerals at each pixel and alteration minerals distribution. The accuracy of alteration mineral extraction refers to the extent which it agrees with a set of reference data measured in the field reconnaissance. So the CASI_SASI airborne hyperspectral image provides the efficient way to map the detailed alteration minerals distribution for mineral exploration in high forest coverage area.

Mineralogy of a perudic Andosol in central Java, Indonesia

DOE Office of Scientific and Technical Information (OSTI.GOV)

Van Ranst, Eric; Utami, S. R.; Verdoodt, A.

2008-02-15

We studied the mineralogy of a perudic Andosol developed on the Dieng Tephra Sequence in central Java, Indonesia. The objective was to confirm the presence and determine the origin and stability of 2:1 and interlayered 2:1 phyllosilicates in well-drained Andosols. This was and still is a debated topic in the literature. Total elemental and selective dissolution, as well as microscopic and X-ray diffraction analyses, were performed on the soil samples collected from this site. These analyses confirmed that andic properties were present in the soil samples. The allophane content determined by selective dissolution was 3-4% in the A horizons, andmore » increased to 12-18% in the deeper subsoil horizons. In addition, the clay fraction contained dioctahedral smectite, hydroxy-Al-interlayered 2:1 minerals (HIS), Al-chlorite, kaolinite, pyrophyllite, mica, cristobalite and some gibbsite. The silt and sand fractions were rich in plagioclase and pyroxene. The 2:1 minerals (smectite and pyrophyllite), as well as chlorite and kaolinite were of hydrothermal origin and were incorporated in the tephra during volcanic eruption. Besides desilication during dissolution of unstable minerals, Al interlayering of 2:1 layer silicates was most likely the most prominent pedogenic process. Although hydroxy-Al polymeric interlayers would normally stabilize the 2:1 clay phases, the strong weakening, and even disappearance of the characteristic XRD peaks, indicated instability of these minerals in the upper A horizons due to the perudic and intensive leaching conditions.« less

The influence of continuous rice cultivation and different waterlogging periods on morphology, clay mineralogy, Eh, pH and K in paddy soils.

PubMed

Bahmanyar, M A

2007-09-01

The effect of different rice cultivation periods on the properties of selected soils in alluvial plain were studied in Mazandaran province (north of Iran) in 2004. Soils were sampled form 0, 6, 16, 26 and over 40 years rice cultivation fields. In each treatment three soil profiles and six nearby auger holes were studied. The present study results indicated that continuous rice cultivation have changed soil moisture regime from xeric to aquic, soil color from brown to grayish, surface horizons from mollic to ochric epipedon and soil structure changed from granular or blocky to massive. Therefore, the soil order has changed from Mollisols to Inceptisols. No illuviation and eluviation of clay minerals occurred as a consequence of rice cultivation. X-ray diffraction analysis showed that clay minerals in non-rice cultivated field were illite, vermiculite, montmorillonite, kaolinite and chlorite, but in rice field were illite, montmorillonite, kaolinite and chlorite, respectively. In contrast of montmorillonite, the amount of illite and vermiculite have been decreased by increasing periods of rice cultivation. The pH values of the saturated soil surface in six weeks past plantation have shifted toward neutrality. While Eh value of non-paddy soils were about +90 mv, surface horizons of paddy soils at field conditions had Eh value about +40, -12, -84, -122 mv, respectively. The amounts of organic matter and available Fe, Mn, Zn and Cu were increased whereas available K was decreased in paddy soils.

Fluid-related inclusions in Alpine high-pressure peridotite reveal trace element recycling during subduction-zone dehydration of serpentinized mantle (Cima di Gagnone, Swiss Alps)

NASA Astrophysics Data System (ADS)

Scambelluri, Marco; Pettke, Thomas; Cannaò, Enrico

2015-11-01

Serpentinites release at sub-arc depths volatiles and several fluid-mobile trace elements found in arc magmas. Constraining element uptake in these rocks and defining the trace element composition of fluids released upon serpentinite dehydration can improve our understanding of mass transfer across subduction zones and to volcanic arcs. The eclogite-facies garnet metaperidotite and chlorite harzburgite bodies embedded in paragneiss of the subduction melange from Cima di Gagnone derive from serpentinized peridotite protoliths and are unique examples of ultramafic rocks that experienced subduction metasomatism and devolatilization. In these rocks, metamorphic olivine and garnet trap polyphase inclusions representing the fluid released during high-pressure breakdown of antigorite and chlorite. Combining major element mapping and laser-ablation ICP-MS bulk inclusion analysis, we characterize the mineral content of polyphase inclusions and quantify the fluid composition. Silicates, Cl-bearing phases, sulphides, carbonates, and oxides document post-entrapment mineral growth in the inclusions starting immediately after fluid entrapment. Compositional data reveal the presence of two different fluid types. The first (type A) records a fluid prominently enriched in fluid-mobile elements, with Cl, Cs, Pb, As, Sb concentrations up to 103 PM (primitive mantle), ∼102 PM Tl, Ba, while Rb, B, Sr, Li, U concentrations are of the order of 101 PM, and alkalis are ∼2 PM. The second fluid (type B) has considerably lower fluid-mobile element enrichments, but its enrichment patterns are comparable to type A fluid. Our data reveal multistage fluid uptake in these peridotite bodies, including selective element enrichment during seafloor alteration, followed by fluid-rock interaction along with subduction metamorphism in the plate interface melange. Here, infiltration of sediment-equilibrated fluid produced significant enrichment of the serpentinites in As, Sb, B, Pb, an enriched trace element pattern that was then transferred to the fluid released at greater depth upon serpentine dehydration (type A fluid). The type B fluid hosted by garnet may record the composition of the chlorite breakdown fluid released at even greater depth. The Gagnone study-case demonstrates that serpentinized peridotites acquire water and fluid-mobile elements during ocean floor hydration and through exchange with sediment-equilibrated fluids in the early subduction stages. Subsequent antigorite devolatilization at subarc depths delivers aqueous fluids to the mantle wedge that can be prominently enriched in sediment-derived components, potentially triggering arc magmatism without the need of concomitant dehydration/melting of metasediments or altered oceanic crust.

A reactive transport model for Marcellus shale weathering

NASA Astrophysics Data System (ADS)

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 fluids. An increase in the water infiltration rate enhanced weathering by removing dissolution products and maintaining far-from-equilibrium conditions. We conclude from these observations that availability of reactive surface area and transport of H2O and gases are the most important factors affecting rates of Marcellus shale weathering of the in the shallow subsurface. This weathering study documents the utility of reactive transport modeling for complex subsurface processes. Such modelling could be extended to understand interactions between injected fluids and Marcellus shale gas reservoirs at higher temperature, pressure, and salinity conditions.

Metamorphic reprocessing of a serpentinized carbonate-bearing peridotite after detachment from the mantle wedge: A P-T path constrained from textures and phase diagrams in the system CaO-MgO-Al 2O 3-SiO 2-CO 2-H 2O

NASA Astrophysics Data System (ADS)

Mposkos, E.; Baziotis, I.; Proyer, A.

2010-08-01

In the central Rhodope mountains of Greece a carbonate-bearing metaperidotite lens ˜ 200 × 500 m in size crops out as part of the high- to ultrahigh-pressure metamorphic Upper Sidironero Complex ˜ 500 m SE of the Gorgona Village, north of Xanthi town. It is composed primarily of coarse grained (3-20 mm in size) olivine and orthopyroxene, medium grained clinohumite and medium to fine grained tremolite, chlorite, dolomite, magnesite, talc, antigorite and various spinel phases. Whole-rock chemistry, mineral textures and compositions, and phase diagram calculations show that the metaperidotite was subjected to a prograde HP metamorphism, isofacial with the surrounding migmatitic gneisses, metapelites and amphibolites. The prograde character of metamorphism is demonstrated by inclusions of talc, antigorite, chlorite, dolomite, magnesite and Ti-clinohumite in ferrit-chromite, olivine, and orthopyroxene, as well as of olivine in orthopyroxene, and by the typical change in composition of zoned spinel minerals from ferrit-chromite in the core to chromian spinel at the rim. The prograde path is characterized by successive growth of amphibole, Ti-clinohumite, olivine and orthopyroxene, followed by the breakdown of Ti-clinohumite to olivine + Mg-ilmenite and of chlorite to olivine + spinel, probably during exhumation. The construction of a partial petrogenetic P- T grid in the system CaO-MgO-Al 2O 3-SiO 2-CO 2-H 2O (CMASCH) for Ca-poor ultramafic bulk compositions has proven highly useful for the reconstruction of the metamorphic evolution and a P- T path, indicating that the use of univariant reactions in mixed volatile systems is highly warranted. The P- T path is clearly constrained to pressures below 1.5-1.7 GPa by the absence of clinopyroxene. These pressures are slightly lower than those recorded in the closely associated Jurassic eclogites and much lower than those recorded in the diamond-bearing gneisses 5 km to the south in the same tectonic unit. The carbonate-bearing metaperidotite from Gorgona probably represents a fragment of the hydrated mantle wedge. This is indicated by the REE compositions which differ from those of ophiolitic peridotites and resemble those of spinel or garnet peridotites of sub-continental origin. The ultramafic slice was incorporated tectonically into the subduction channel, most likely by tectonic erosion in the Early Jurassic, but did not experience ultrahigh-pressure metamorphism like the nearby metapelites that exhumed along the same subduction channel.

Fluid-induced Blueschist Preservation on Syros, Cyclades, Southern Greece

NASA Astrophysics Data System (ADS)

Kleine, B. I.; Huet, B.; Skelton, A. D. L.

2012-04-01

Local examples of preservation of high-pressure, low-temperature (HP-LT) mineral assemblages within retrograde metamorphosed greenschist are recorded from the Cyclades, Greece. Several models have been proposed to explain the preservation of HP-LT rocks in these areas. On Sifnos, a capping effect of impermeable marble units below the preserved blueschists caused diversion of the upward, cross-layer infiltration of retrograde fluids [1]. On Tinos, blueschist preservation occurred due to retrograde fluid flow channelization along lithological contacts with high flux rates [2]. HP-LT minerals were preserved in regions adjacent to these contacts where fluid fluxes were smaller. We propose a different mechanism of blueschist preservation based on observations from a costal section near Fabrika on Syros. At this locality a high strain zone cuts through a retrograde greenschist. Along the fault a dark blue halo occurs within the greenschist. Whole rock analyses along a profile from the fault into the greenschist show that only the areas directly adjacent to the deformation zone show chemical evidence of metasomatism, whereas the areas further away are chemically similar to greenschist. Point counting of 1000 evenly spaced points in thin sections of the profile shows a clear blueschist to greenschist transition with a blueschist mineral assemblage (glaucophane+phengite+calcite) nearer to the metasomatic zone and a typical greenschist mineral assemblage (epidote+chlorite+albite) farther away. We propose the following model to explain preservation of HP-LT mineral assemblage in this locality. During retrograde metamorphism a water-rich fluid infiltrated the blueschist rock from below. This occurred close to the brittle-ductile transition. This fluid caused a reaction front to propagate into the overlying blueschist at which its mineral assemblage glaucophane+phengite+calcite was replaced by the greenschist mineral assemblage epidote+albite+chlorite. Upwards-flowing fluid passing through the reaction front is buffered to higher X(CO2) by the reaction glaucophane+phengite+calcite+H2O=albite+chlorite+epidote+quartz+CO2. This fluid travels faster along paths of structural weakness (e.g. shear zones, faults). If this fluid reaches colder regions more rapidly such that the fluid chemistry is unable to "keep up" with the position of the reaction equilibria as the temperature falls, X(CO2) will be effectively shifted back into the blueschist stability field and blueschist will be preserved, specifically within high flux regions, such as shear zones and faults. [1] Matthews & Schliestedt (1984), Contributions to Mineralogy and Petrology, 88, 150-163. [2] Breeding et al. (2003), Geochemistry Geophysics Geosystems, 4, 1-11.

Combination of sodium chlorite and calcium propionate reduces enzymatic browning and microbial population of fresh-cut "Granny Smith" apples.

PubMed

Guan, Wenqiang; Fan, Xuetong

2010-03-01

Tissue browning and microbial growth are the main concerns associated with fresh-cut apples. In this study, effects of sodium chlorite (SC) and calcium propionate (CP), individually and combined, on quality and microbial population of apple slices were investigated. "Granny Smith" apple slices, dipped for 5 min in CP solutions at 0%, 0.5%, 1%, and 2% (w/v) either alone or in combination with 0.05% (w/v) SC, were stored at 3 and 10 degrees C for up to 14 d. Color, firmness, and microflora population were measured at 1, 7, and 14 d of storage. Results showed that CP alone had no significant effect on the browning of cut apples. Even though SC significantly inhibited tissue browning initially, the apple slices turned brown during storage at 10 degrees C. The combination of CP and SC was able to inhibit apple browning during storage. Samples treated with the combination of SC with CP did not show any detectable yeast and mold growth during the entire storage period at 3 degrees C. At 10 degrees C, yeast and mold count increased on apple slices during storage while CP reduced the increase. However, high concentrations of CP reduced the efficacy of SC in inactivating E. coli inoculated on apples. Overall, our results suggested that combination of SC with 0.5% and 1% CP could be used to inhibit tissue browning and maintain firmness while reducing microbial population. Practical Application: Apple slices, which contain antioxidants and other nutrient components, have emerged as popular snacks in food service establishments, school lunch programs, and for family consumption. However, the further growth of the industry is limited by product quality deterioration caused by tissue browning, short shelf-life due to microbial growth, and possible contamination with human pathogens during processing. Therefore, this study was conducted to develop treatments to reduce microbial population and tissue browning of "Granny Smith" apple slices. Results showed that an antimicrobial compound, sodium chlorite, is effective in not only eliminating microbes but also inhibiting tissue browning of apple slices. However, the compound caused tissue softening and its antibrowning effect was short-lived, lasting only for a few days. Combination of the compound with a calcium-containing food additive was able to improve firmness and freshness of apple slices while reducing population of Escherichia coli artificially inoculated on samples and inhibiting the growth of yeast and mold during storage.

Modelling Iron-Bentonite Interactions

NASA Astrophysics Data System (ADS)

Watson, C.; Savage, D.; Benbow, S.; Wilson, J.

2009-04-01

The presence of both iron canisters and bentonitic clay in some engineered barrier system (EBS) designs for the geological disposal of high-level radioactive wastes creates the potential for chemical interactions which may impact upon the long-term performance of the clay as a barrier to radionuclide migration. Flooding of potential radionuclide sorption sites on the clay by ferrous ions and conversion of clay to non-swelling sheet silicates (e.g. berthierine) are two possible outcomes deleterious to long-term performance. Laboratory experimental studies of the corrosion of iron in clay show that corrosion product layers are generally thin (< 1 µm) with magnetite, siderite, or ‘green rust' occurring depending upon temperature and ambient partial pressure of carbon dioxide. In theory, incorporation of iron into clay alteration products could act as a ‘pump' to accelerate corrosion. However, the results of laboratory experiments to characterise the products of iron-bentonite interaction are less than unequivocal. The type and amounts of solid products appear to be strong functions of time, temperature, water/clay ratio, and clay and pore fluid compositions. For example, the products of high temperature experiments (> 250 °C) are dominated by chlorite, whereas lower temperatures produce berthierine, odinite, cronstedtite, or Fe-rich smectite. Unfortunately, the inevitable short-term nature of laboratory experimental studies introduces issues of metastability and kinetics. The sequential formation in time of minerals in natural systems often produces the formation of phases not predicted by equilibrium thermodynamics. Evidence from analogous natural systems suggests that the sequence of alteration of clay by Fe-rich fluids will proceed via an Ostwald step sequence. The computer code, QPAC, has been modified to incorporate processes of nucleation, growth, precursor cannibalisation, and Ostwald ripening to address the issues of the slow growth of bentonite alteration products. This, together with inclusion of processes of iron corrosion and diffusion, has enabled investigation of a representative model of the alteration of bentonite in a typical EBS environment. Simulations with fixed mineral surface areas show that berthierine dominates the solid product assemblage, with siderite replacing it at simulation times greater than 10 000 years. Simulations with time-dependent mineral surface areas show a sequence of solid alteration products, described by: magnetite -> cronstedtite -> berthierine -> chlorite. Using plausible estimates of mineral-fluid interfacial free energies, chlorite growth is not achieved until 5 000 years of simulation time. The results of this modelling work suggest that greater emphasis should be placed upon methods to up-scale the results of laboratory experiments to timescales of relevance to performance assessment.

Mineralogical and Geochemical Study of Titanite Associated With Copper Mineralization in the Hopper Property, Yukon Territory, Canada

NASA Astrophysics Data System (ADS)

Blumenthal, V. H.; Linnen, R. L.

2009-05-01

Copper mineralization in central Yukon is well known, but the metallogeny of the Ruby Range batholith, west of the copper belt, is poorly understood. The Hopper property, situated in the south western part of the Yukon in the Yukon-Tanana terrane, contains copper mineralization hosted by granodiorite and quartz feldspar porphyry of cal-alkaline affinity. These rock units, interpreted to be part of the Ruby Range batholith, intruded metasediments of the Ashihik Metamorphic Suite rocks. Mafic dykes cross cut the intrusion followed by aplite dykes. Small occurrences of skarn also occur in the area and some of these contain copper mineralization. The copper mineralization at the Hopper property appears to have a porphyry-type affinity. However, it is associated with a shear zone and propylitic alteration unlike other typical copper porphyry-type deposits. This raises the question whether or not the mineralization is orthomagmatic in origin, i.e., whether or not this is a true porphyry system. The main zone of mineralization is 1 kilometer long and 0.5 kilometer wide. It is characterized by disseminated chalcopyrite and pyrite, which also occur along fractures. Molybdenite mineralization was found to be associated with slickensides. Alteration minerals associated with the copper mineralization are chlorite, epidote-clinozoisite, carbonate and titanite. Chlorite and epidote-clinozoisite are concentrated in the mineralized zone, whereas an earlier potassic alteration shows a weaker spatial correlation with the mineralization. The association of the mineralization with propylitic alteration leads us to believe the mineralization is shear related, although a deeper porphyritic system may be present at depth. Two populations of titanite at the Hopper property are recognized based on their shape, size and association with other minerals. The first population, defined by a length of 100 micrometers to 1 centimeter, euhedral boundaries, and planar contacts with other magmatic phases, is interpreted to be magmatic in origin. The second population is 10 to 500 micrometers long, anhedral and shows a close association with chlorite and chalcopyrite. This type of titanite is hydrothermal in origin. Preliminary electron microprobe analyses of titanite show the magmatic titanite grains have higher concentrations of Al, Fe, Nb, Ce, Zr and Mn, and lower concentrations of Ti and Ca compared to hydrothermal titanite grains. This corresponds with substitutions of Al, Fe, Nb, and Ce to Ti and substitutions of Ce, Zr to Ca. The association of titanite with propylitic alteration and its susceptibility to trace element substitutions make this an ideal test case to evaluate magmatic versus hydrothermal titanite.

Mineral resource of the month: Vermiculite

USGS Publications Warehouse

Tanner, Arnold O.

2014-01-01

Vermiculite comprises a group of hydrated, laminar magnesium-aluminum-iron silicate minerals resembling mica. They are secondary minerals, typically altered biotite, iron-rich phlogopite or other micas or clay-like minerals that are themselves sometimes alteration products of amphibole, chlorite, olivine and pyroxene. Vermiculite deposits are associated with volcanic ultramafic rocks rich in magnesium silicate minerals, and flakes of the mineral range in color from black to shades of brown and yellow. The crystal structure of vermiculite contains water molecules, a property that is critical to its processing for common uses.

Geotechnical Data Inventory, Southern California Coastal Zone, Cape San Martin (Monterey County) to Mexican Border.

DTIC Science & Technology

1985-12-01

Adequate Several moderate to snail Santa Ynez Mts. sized creeks and streams The largest potential source for sediment is La Honda Canyon. Major drainage...Sized or Area Relative Size Sediment Rate Drainage Basin(s) Santa Ynez River (See note 5) Large 48,000 cu. yds./yr. Ref: 66 Honda Ck (See note 5) Small...Hematite- Ilmenite, Epidote. Ref: 4A Heavy Minerals* Ref: 56A Epidote Augite Hornblende Chlorite Opaques Los Angeles 9 6 23 12 33 Cliffs Laguna Beach "Coarse

Mineralogical, geochemical and radiological characterisation of Selmo Formation in Batman area, Turkey.

PubMed

Isik, Umit; Damla, Nevzat; Akkoca, Dicle Bal; Cevik, Uğur

2012-06-01

This work deals with the mineralogical, geochemical and radiological characterisations of Selmo Formation in Batman neighbourhood. The upper Miocene-Pliocene Selmo Formation is common in the centre of Batman and composed of carbonated sandy claystones and silty-sandy stone lenses. The common whole minerals of the samples are quartz, feldspars, calcite and dolomite. The clay minerals are smectite, illite, chlorite and mixed-layer clay (chlorite-smectite). The geochemical mean values of the samples are 51.7% SiO(2); 12.6% Al(2)O(3); 6.2% Fe(2)O(3); 3.6% MgO; 6.3% CaO; 1.1% Na(2)O; 1.7% K(2)O; 0.8% TiO(2); 0.2% P(2)O(5); 0.1% MnO; and 0.03% Cr(2)O(3). In addition, baseline maps for the concentrations of each radionuclide, the radium equivalent activity and the outdoor gamma dose rate distributions have been plotted for the study area. The mean activity concentrations of (226)Ra, (232)Th, (40)K and (137)Cs were determined to be 32, 24, 210 and 9 Bq kg(-1), respectively. The assessments of the radiological hazard indices, such as radium equivalent activity, absorbed dose rate in air, annual effective dose equivalent, excess lifetime cancer risk, external hazard index and internal hazard index, were calculated and compared with the internationally accepted reference values. This study shows that the concentrations of radioactivities in the measured samples were within the recommended safety limits and did not pose to be any significant source of radiation hazard.

The efficacy and safety of add-on 0.1% brimonidine tartrate preserved with sodium chlorite in on-treatment Japanese normal-tension glaucoma patients.

PubMed

Tsumura, Toyoaki; Yoshikawa, Keiji; Kimura, Tairo; Suzumura, Hirotaka; Kawashima, Miwako; Nanno, Mami; Ishijima, Kiyotaka; Takeda, Ryuji

2014-01-01

To evaluate the efficacy and safety of newly formulated brimonidine (0.1% brimonidine tartrate preserved with sodium chlorite: brimonidine) as add-on therapy in on-treatment Japanese normal-tension glaucoma (NTG) patients. Brimonidine was added to on-treatment NTG patients with intraocular pressures (IOP) of between 13 mmHg and 16 mmHg after three consecutive IOP measurements. The time courses of IOP, conjunctival hyperemia, superficial punctate keratitis, and adverse events were examined at 4, 8, and 12 weeks after brimonidine instillation. Though 75 of 83 patients (31 males and 52 females; mean age: 63.4±11.6 years) completed the study, six patients discontinued because of side effects and two patients withdrew. The mean IOP after brimonidine addition at week 4 (12.6±1.8 mmHg, P<0.001), week 8 (12.4±1.7 mmHg, P<0.001), and week 12 (12.6±1.8 mmHg, P<0.001) was significantly decreased compared with that before the addition of brimonidine (13.9±1.2 mmHg). No significant changes in superficial punctate keratitis or conjunctival hyperemia scores were observed throughout the study. Dizziness, sleepiness, eye pain, and itching (mild to moderate) were noted in five, four, three, and three patients, respectively. The addition of newly formulated brimonidine to on-treatment Japanese NTG patients with IOP of 13-16 mmHg further reduced the levels of IOP with minimal side effects and adverse events.

Origin of the Okrouhlá Radouň episyenite-hosted uranium deposit, Bohemian Massif, Czech Republic: fluid inclusion and stable isotope constraints

NASA Astrophysics Data System (ADS)

Dolníček, Zdeněk; René, Miloš; Hermannová, Sylvie; Prochaska, Walter

2014-04-01

The Okrouhlá Radouň shear zone hosted uranium deposit is developed along the contact of Variscan granites and high-grade metasedimentary rocks of the Moldanubian Zone of the Bohemian Massif. The pre-ore pervasive alteration of wall rocks is characterized by chloritization of mafic minerals, followed by albitization of feldspars and dissolution of quartz giving rise to episyenites. The subsequent fluid circulation led to precipitation of disseminated uraninite and coffinite, and later on, post-ore quartz and carbonate mineralization containing base metal sulfides. The fluid inclusion and stable isotope data suggest low homogenization temperatures (˜50-140 °C during pre-ore albitization and post-ore carbonatization, up to 230 °C during pre-ore chloritization), variable fluid salinities (0-25 wt.% NaCl eq.), low fluid δ18O values (-10 to +2 ‰ V-SMOW), low fluid δ13C values (-9 to -15 ‰ V-PDB), and highly variable ionic composition of the aqueous fluids (especially Na/Ca, Br/Cl, I/Cl, SO4/Cl, NO3/Cl ratios). The available data suggest participation of three fluid endmembers of primarily surficial origin during alteration and mineralization at the deposit: (1) local meteoric water, (2) Na-Ca-Cl basinal brines or shield brines, (3) SO4-NO3-Cl-(H)CO3 playa-like fluids. Pre-ore albitization was caused by circulation of alkaline, oxidized, and Na-rich playa fluids, whereas basinal/shield brines and meteoric water were more important during the post-ore stage of alteration.

Peptide Biomarkers as Evidence of Perchlorate Biodegradation▿ †

PubMed Central

Bansal, Reema; Crawford, Ronald L.; Paszczynski, Andrzej J.

2011-01-01

Perchlorate is a known health hazard for humans, fish, and other species. Therefore, it is important to assess the response of an ecosystem exposed to perchlorate contamination. The data reported here show that a liquid chromatography-mass spectrometry-based proteomics approach for the detection of perchlorate-reducing enzymes can be used to measure the ability of microorganisms to degrade perchlorate, including determining the current perchlorate degradation status. Signature peptides derived from chlorite dismutase (CD) and perchlorate reductase can be used as biomarkers of perchlorate presence and biodegradation. Four peptides each derived from CD and perchlorate reductase subunit A (PcrA) and seven peptides derived from perchlorate reductase subunit B (PcrB) were identified as signature biomarkers for perchlorate degradation, as these sequences are conserved in the majority of the pure and mixed perchlorate-degrading microbial cultures examined. However, chlorite dismutase signature biomarker peptides from Dechloromonas agitata CKB were found to be different from those in other cultures used and should also be included with selected CD biomarkers. The combination of these peptides derived from the two enzymes represents a promising perchlorate presence/biodegradation biomarker system. The biomarker peptides were detected at perchlorate concentrations as low as 0.1 mM and at different time points both in pure cultures and within perchlorate-reducing environmental enrichment consortia. The peptide biomarkers were also detected in the simultaneous presence of perchlorate and an alternate electron acceptor, nitrate. We believe that this technique can be useful for monitoring bioremediation processes for other anthropogenic environmental contaminants with known metabolic pathways. PMID:21115710

Oxygen-isotope exchange and mineral alteration in gabbros of the Lower Layered Series, Kap Edvard Holm Complex, East Greenland

USGS Publications Warehouse

Fehlhaber, Kristen L.; Bird, Dennis K.

1991-01-01

Multiple intrusions of gabbros, mafic dikes, and syenites in the Kap Edvard Holm Complex gave rise to prolonged circulation of meteoric hydrothermal solutions and extreme isotope exchange and mineral alteration in the 3600-m-thick Lower Layered Series gabbros. In the Lower Layered Series, δ18O of plagioclase varies from +0.3‰ to -5.8‰, and it decreases with an increase in the volume of secondary talc, chlorite, and actinolite. In the same gabbros, pyroxenes have a more restricted range in δ18O, from 5.0‰ to 3.8‰ and values of δ18Opyroxene are independent of the abundance of secondary minerals, which ranges from 14% to 30%. These relations indicate that large amounts of water continued to flow through the rocks at temperatures of <500-600°C, altering the gabbros to assemblages of talc + chlorite + actinolite ± epidote ±albite and causing significant oxygen-isotope exchange in plagioclase, but not in pyroxene. The extensive low-temperature secondary mineralization and 18O depletion of plagioclase in the Lower Layered Series are associated with the later emplacement of dikes and gabbros and syenites, which created new fracture systems and provided heat sources for hydrothermal fluid circulation. This produced subsolidus mineral alteration and isotope exchange in the Lower Layered Series that are distinct from those in the Skaergaard and Cuillin gabbros of the North Atlantic Tertiary province, but are similar to those observed in some oceanic gabbros.

Phanerozoic extensional faulting and alteration control on uranium mineralization in trachytes of the Central Eastern Desert of Egypt

NASA Astrophysics Data System (ADS)

Hamdy, Mohamed M.; Waheeb, Anton G.; Aly, Samir M.; Farag, Nagdy M.; Sadek, Adel F.

2017-12-01

The Gabal Nasb El Atshan Upper Carboniferous-Lower Permian altered trachytes include uranium up to 3165 ppm. The paleostress and resolved shear stress analyses of the deformation systems in Gabal Nasb El Atshan area indicate that the trachyte was subjected to WNW-ESE to E-W tensile shear stress directed extensional regimes. The low-stress regions in the vicinity of extensional faults and their associated joints were favorable locations for fluid flow and the consequence alteration and U-mineralization. This occurred more extensively along the contacts between the sills of trachyte and the Hammamat sedimentary rocks; where the latter acted as a physical barrier for the alteration fluids migration outward. Alteration styles include albitization, aegirinization, arfvedsonization, chloritization and ferruginisation. The albitization is the most common sodic metasomatism, giving sanidine from Or98.8Ab0.7 to Or62.3Ab37.6, anorthoclase from Or51.4Ab48.0 to Or12.2Ab87.6 and albite from Or11.0Ab89.0 to Or0.8Ab99.2. Aegirine and arfvedsonite formed due to decreasing sodium activity in the metasomatic fluids. Sodic metasomatism may be the source of uranium-enrichment, taking place during the late magmatic to deuteric processes. This was followed by a retrograde alteration of chloritization between 175 and 42 °C toward precipitation of Fe-oxides and alteration of primary uranium. Surficial low-temperature alteration remobilized and redistributed the produced uranylhydroxides and ferruginisation caused the reduction and adsorption of U forming betafite, uranophane, soddyite, umohoite, uranotile and uranopilite.

Depositional environment, sand provenance, and diagenesis of the Basal Salina Formation (lower Eocene), northwestern Peru

NASA Astrophysics Data System (ADS)

Marsaglia, K. M.; Carozzi, A. V.

The Basal Salina Formation is a lower Eocene transgressive sequence consisting of interbedded shales, siltstones, and conglomeratic sandstones. This formation occurs in the Talara basin of northwestern Peru and is one of a series of complexly faulted hydrocarbon-producing formations within this extensional forearc basin. These sediments were probably deposited in a fan-delta complex that developed along the ancestral Amotape Mountains during the early Eocene. Most of the sediment was derived from the low-grade metamorphic and plutonic rocks that comprise the Amotape Mountains, and their sedimentary cover. Detrital modes of these sandstones reflect the complex tectonic history of the area, rather than the overall forearc setting. Unlike most forearc sediments, these are highly quartzose, with only minor percentages of volcanic detritus. This sand is variably indurated and cemented by chlorite, quartz, calcite, and kaolinite. Clay-mineral matrix assemblages show gradational changes with depth, from primarily detrital kaolinite to diagenetic chlorite and mixed-layered illite/smectite. Basal Salina sandstones exhibit a paragenetic sequence that may be tied to early meteoric influx or late-stage influx of thermally driven brines associated with hydrocarbon migration. Much of the porosity is secondary, resulting from a first-stage dissolution of silicic constituents (volcanic lithic fragments, feldspar, and fibrous quartz) and a later dissolution of surrounding carbonate cement. Types of pores include skeletal grains, grain molds, elongate pores, and fracture porosity. Measured porosity values range up to 24% and coarser samples tend to be more porous. Permeability is enhanced by fractures and deterred by clay-mineral cements and alteration residues.

Adsorption of organic ligands on low surface charge clay minerals: the composition in the aqueous interface region.

PubMed

Jelavić, S; Stipp, S L S; Bovet, N

2018-06-27

An understanding of the mechanisms that control the adsorption of organic molecules on clay minerals is of interest in several branches of science and industry. Oil production using low salinity injection fluids can increase yields by as much as 40% over standard injection with seawater or formation water. The mechanism responsible for the low salinity response is still debated, but one hypothesis is a change in pore surface wettability. Organic contamination in soil and drinking water aquifers is a challenge for municipal water suppliers and for agriculture. A better understanding is needed for how mineral species, solution composition and pH affect the desorption of low molecular weight organic ligands from clay minerals and consequently their wettability. We used X-ray photoelectron spectroscopy under cryogenic conditions to investigate the in situ composition in the mineral-solution interface region in a series of experiments with a range of pH and ion concentrations. We demonstrate that both chlorite and kaolinite release organic molecules under conditions relevant for low salinity water flooding. This release increases with a higher solution pH but is only slightly affected by the character of the organic ligand. This is consistent with the observation that low salinity enhanced oil recovery correlates with the presence of chlorite and kaolinite. Our results indicate that the pore surface charge and salinity of formation water and injection fluids are key parameters in determining the low salinity response. In general, our results imply that clay mineral surface charge influences the composition in the interface through an affinity for organic molecules.

Distribution and composition of gold in porphyry gold systems: example from the Biely Vrch deposit, Slovakia

NASA Astrophysics Data System (ADS)

Koděra, Peter; Kozák, Jaroslav; Brčeková, Jana; Chovan, Martin; Lexa, Jaroslav; Jánošík, Michal; Biroň, Adrián; Uhlík, Peter; Bakos, František

2018-03-01

The Biely Vrch deposit in the Western Carpathians is assigned to the shallow, sulfide-poor porphyry gold deposit type and has an exceptionally low Cu/Au ratio. According to 3-D geochemical models, there is a limited spatial correlation between Au and Cu due to the primary introduction of gold by a salt melt and Cu by low-density vapor. Despite a rough spatial correlation of gold grades with quartz stockwork intensity, gold is hosted mostly by altered rock, exclusively in native form. Three main gold mineral assemblages were recognized here. In the deepest parts of the system, the K- and Ca-Na silicate gold assemblage is associated with minerals of high-temperature alteration (plagioclase, K-feldspar, actinolite), with gold grades and fineness depending on depth and potassium content of the host rock: K-silicate alteration hosts the lowest fineness gold ( 914), whereas Ca-Na silicate alteration has the highest ( 983). The intermediate argillic gold assemblage is the most widespread, with gold hosted mainly by chlorite, illite, smectite, and interstratified illite-chlorite-smectite minerals. The gold fineness is mostly variable (875-990) and inherited from the former gold mineral assemblages. The latest advanced argillic gold assemblage has its gold mostly in kaolinite. The extremely high fineness ( 994) results from gold remobilization by late-stage aqueous magmatic-hydrothermal fluids. Uncommon bonanza-grade appears where the earlier gold mineral assemblages were further enriched by this remobilized gold. Primary precipitation of gold occurred during ascent and cooling of salt melts at 450 to 309 °C, mostly during retrograde quartz solubility.

The Žermanice sill: new insights into the mineralogy, petrology, age, and origin of the teschenite association rocks in the Western Carpathians, Czech Republic

NASA Astrophysics Data System (ADS)

Matýsek, Dalibor; Jirásek, Jakub; Skupien, Petr; Thomson, Stuart N.

2018-04-01

The Žermanice locality represents the best-exposed example of the meta-basaltoid/meta-gabbroic rock type of the teschenite association. It forms a subhorizontal volcanic body (sill) 27-30 m thick. The subvolcanic rock is inhomogeneous and slightly differentiated. The predominant rock type is a basaltoid (diabase-dolerite), medium-grained, speckled, mesocratic rock exhibiting an evident subophitic texture. Miarolitic cavities are abundant in some places. The major rock constituents are albite, microcline, chlorite, and pyroxene, as well as analcime and plagioclase in places. The accessory magmatic phases are biotite, ilmenite, fluorapatite, sulphides, Ti-rich magnetite, Nb-rich baddeleyite, and chevkinite-(Ce) or perrierite-(Ce). A large extent of alteration is evident from the presence of chloritization, albitization of plagioclases, and zeolitization (analcimization). Geochemical analyses reveal an affinity for metaluminous igneous rocks. The best fit is with the within-plate basalts or the within-plate volcanic zones. The classification of this rock is problematic because of the mixed intrusive and extrusive features; the choice is between meta-alkali basalt and metadolerite (meta-microgabbro). 207Pb common lead-corrected U-Pb apatite dating yields a weighted mean age of 120.4 ± 9.6 Ma, which corresponds to the middle Aptian. The igneous body is at most ca. 10 Ma younger than the surrounding late Hauterivian sediments and might have been emplaced into unconsolidated or partly consolidated sediments. According to our research, it is evident that at least some teschenite association rocks are in fact low-grade metamorphic rocks.

Metallogenic and tectonic significance of oxygen isotope data and whole-rock potassium-argon ages of the Nikolai Greenstone, McCarthy Quadrangle, Alaska

USGS Publications Warehouse

Silberman, M.L.; MacKevett, E.M.; Connor, C.L.; Matthews, Alan

1980-01-01

The Middle and (or) Late Triassic Nikolai Greenstone, part of the allochthonous terrane of Wrangellia, is typically altered and locally metamorphosed to prehnite-pumpellyite facies with chlorite and epidote as the most common secondary minerals. Intrinsic copper content averages 155 ppm, and two types of concentrations of copper in the Nikolai are common: (1) native copper fillings of amygdules and rubble zones typically near flow tops, and (2) veins and thin replacement zones that contain native copper and copper-iron sulfides in quartz-epidote or calcite gangue in faults and fractures. Oxygen isotope data from quartz and epidote from three copperbearing veins yield calculated ore fluid temperatures of approximately 200°C and 6180 of approximately +1 per mil in agreement with a metamorphicsegregation origin of these deposits, as suggested by Sinclair (1977). Seven K-Ar ages of chloritized greenstone, including those adjacent to veins fall on an initial argon diagram with a zero intercept and a slope which yields an isochron age of 112 + 11 m.y. The ages define a Cretaceous thermalmetamorphic episode which is responsible for alteration and mineralization. The episode is younger than a major Jurassic progeny, accompanied by granitic intrusion, in the area, and appears to be unaffected by minor granitic intrusion in the middle to late Tertiary. We believe the Cretaceous event is related to accretion of Wrangellia to its present relative position in North America. This age of accretion agrees with stratigraphic and structural evidence cited by other workers. 

Fluvial/lacustrine diagenesis: Significance for hydrocarbon production and entrapment in the carboniferous Albert Fm, Moncton basin, NB

DOE Office of Scientific and Technical Information (OSTI.GOV)

Noble, J.P.A.; Chowdhury, A.H.; Yu, H.

1996-12-31

The Carboniferous Horton Group Albert Formation sediments include lacustrine source-rock oil shales and fluvial porous reservoir sandstones. The petrography, stable isotopes, fluid inclusions, cathodoluminescence and mirror/trace element chemistry of these sandstones are used to establish the diagenetic history and controlling factors. Early diagenetic calcite, quartz and albite cements with minor chlorite and kaolinite are variably present and related to depositional mineralogy and lake levels winch controlled the porewater chemistry. Antitaxial veins occurring preferentially in shales are shown, from heavy {delta}C{sup 13} values and fluid inclusions, to be related to methanogenesis in overpressured zones at shallow depths. Later burial calcite andmore » extensive albitisation are related to mineral reactions during the phase of rapid subsidence at temperatures of 80{degrees} to 150{degrees} in the deepest segment of the basin, together with significant dissolution of carbonates and feldspars related mainly to organic acids generated by organic maturation processes. Mass balance calculations indicate that not enough organic matter was present to account for all the estimated secondary porosity and some evidence suggests that reactions between kaolinite and calcite/ankerite to produce chlorite, and mixed layer illite-smectite ordering reactions, produced significant secondary porosity. Burial history reconstructions and thermal modelling of the Albert Fm. sediments using Arrhenius type maturity models and reflectance and rock-eval data suggest locally variable maturation and reservoir production related to the locally different fault tectonic histories characteristic of strike-slip lacustrine segmented basins. The Horton depositional cycle was followed by major dextral transpression with local faulting and inversion and vein cementation.« less

Fluvial/lacustrine diagenesis: Significance for hydrocarbon production and entrapment in the carboniferous Albert Fm, Moncton basin, NB

DOE Office of Scientific and Technical Information (OSTI.GOV)

Noble, J.P.A.; Chowdhury, A.H.; Yu, H.

1996-01-01

The Carboniferous Horton Group Albert Formation sediments include lacustrine source-rock oil shales and fluvial porous reservoir sandstones. The petrography, stable isotopes, fluid inclusions, cathodoluminescence and mirror/trace element chemistry of these sandstones are used to establish the diagenetic history and controlling factors. Early diagenetic calcite, quartz and albite cements with minor chlorite and kaolinite are variably present and related to depositional mineralogy and lake levels winch controlled the porewater chemistry. Antitaxial veins occurring preferentially in shales are shown, from heavy [delta]C[sup 13] values and fluid inclusions, to be related to methanogenesis in overpressured zones at shallow depths. Later burial calcite andmore » extensive albitisation are related to mineral reactions during the phase of rapid subsidence at temperatures of 80[degrees] to 150[degrees] in the deepest segment of the basin, together with significant dissolution of carbonates and feldspars related mainly to organic acids generated by organic maturation processes. Mass balance calculations indicate that not enough organic matter was present to account for all the estimated secondary porosity and some evidence suggests that reactions between kaolinite and calcite/ankerite to produce chlorite, and mixed layer illite-smectite ordering reactions, produced significant secondary porosity. Burial history reconstructions and thermal modelling of the Albert Fm. sediments using Arrhenius type maturity models and reflectance and rock-eval data suggest locally variable maturation and reservoir production related to the locally different fault tectonic histories characteristic of strike-slip lacustrine segmented basins. The Horton depositional cycle was followed by major dextral transpression with local faulting and inversion and vein cementation.« less

Hydrothermal alteration, ore fluid characteristics, and gold depositional processes along a trondhjemite-komatiite contact at Tarmoola, Western Australia

USGS Publications Warehouse

Duuring, P.; Hagemann, S.G.; Cassidy, K.F.; Johnson, C.A.

2004-01-01

Tarmoola is a structurally controlled Archean orogenic gold deposit hosted in greenschist facies metamorphosed komatiite and trondhjemite in the Leonora district of the Eastern Goldfields province, Yilgarn craton. High-grade (>1 g/t Au) orebodies are located in komatiite wall rock adjacent to the eastern and northeastern margins of the asymmetrical, north-south-striking, Tarmoola trondhjemite intrusion. Gold-bearing veins post-date trondhjemite emplacement (ca. 2700 Ma), quartz diorite dikes (ca. 2667 Ma), and regional greenschist facies metamorphism. Textures and crosscutting relationships in gold-bearing veins indicate two stages of hydrothermal fluid infiltration associated with a single gold-related hydrothermal event: a volumetrically dominant, but gold-poor, stage I fluid and a gold-rich stage II fluid. Gold-bearing veins contain stage I milky quartz and pyrite that are overprinted by stage II quartz-ankerite-muscovite-chalcopyrite-sphalerite-galena-gold-tellurides ?? albite ?? chlorite ?? fuchsite ?? epidote ?? scheelite. Stage I hydrothermal alteration assemblages are different in trondhjemite and komatiite due to contrasting reactions between a common ore fluid and disparate wall-rock chemistry. Stage II fluid-wall rock interaction was minor compared to stage I and is indicated by the overprinting of stage I mineral assemblages by stage II microveins. Wall-rock alteration proximal to veins in trondhjemite is characterized by replacement of igneous plagioclase, amphibole, biotite, and metamorphic chlorite by hydrothermal quartz, muscovite, ankerite, calcite, pyrite, chalcopyrite, sphalerite, galena, tellurides, and gold, whereas in proximal alteration in komatiite, metamorphic chlorite and talc are replaced by ankerite, quartz, muscovite, albite, chlorite, fuchsite, pyrite, chalcopyrite, sphalerite, galena, tellurides, and gold. The stage II fluid was enriched in H2O, CO2, Si, Ca, K, Na, S, Au, Ag, Cu, Pb, W, Bi, As, Mo, Zn, and Te. Based on fluid inclusion studies and stage II mineral equilibria, gold deposited from a homogeneous, neutral to slightly alkaline (pH 5.1-5.5), reduced, low-salinity (<5.5 wt % NaCl equiv) fluid that had a bulk composition of 78 mole percent H2O and 21 mole percent CO2, and trace amounts of CH4, C2H6, H2, Ar, H2S, and He. Gold deposition occurred at 300?? ?? 50??C and 0.5 to 3.0 kbars. Assuming lithostatic fluid pressures, gold precipitated at a 2- to 10-km depth. Stage II gray quartz ??18Ofluid values range from 5.9 to 7.5 per mil, whereas ??Dfluid values calculated from the dehydration of muscovite grains and measured directly from bulk fluid inclusion analyses of stage II gray quartz have ranges of -9 to -35 and -27 to -28 per mil, respectively. Hydrothermal ore fluids were transported from greater crustal depths to the site of gold deposition during the district-scale D3 event by shallowly W dipping, reverse brittle-ductile shear zones in supracrustal rock and along the steeply east dipping trondhjemite contact. Associated subhorizontal east-west shortening caused the reactivation of the eastern trondhjemite margin and subparallel foliation, which facilitated the transport of hydrothermal fluids and the generation of gold-bearing veins and hydrothermal alteration zones in komatiite. East-west-striking fractures in trondhjemite aided the lateral migration of ore fluids away from trondhjemite margins and the formation of east-west-striking gold-bearing veins and broad alteration zones. Gold was most likely transported in the stage II fluid as bisulfide complexes. The sulfidation of trondhjemite and komatiite wall rock by the stage II fluid caused the destabilization of An bisulfide complexes and gold deposition. Potassium, Ca, and CO2 metasomatism of komatiite wall rock may have enhanced gold deposition via the acidification of the stage II fluid. The physicochemical characteristics of the Tarmoola ore fluid and relative timing of gold mineralization are consistent with the Yilgarn-wide,

Aqueous Alteration of the Grosnaja CV3 Carbonaceous Chondrite

NASA Astrophysics Data System (ADS)

Keller, L. P.; McKay, D. S.

1993-07-01

Previous petrographic studies have shown that aqueous alteration products are locally well developed in some of the CV3 falls [e.g., 1-3]. In this abstract, we describe our transmission electron microscope (TEM) study of the extent of aqueous alteration in matrix and in chondrules in the Grosnaja CV3 carbonaceous chondrite. Grosnaja is an observed fall and belongs to the oxidized subgroup of the CV chondrites [4]. We obtained fragments of Grosnaja from the Naturhistorisches Museum in Vienna. Regions of interest were extracted from polished thin sections and prepared for TEM observation by ion milling. Quantitative energy-dispersive X-ray (EDX) analyses were obtained using a JEOL 2000FX TEM equipped with a LINK thin- window EDX detector. Grosnaja has undergone aqueous alteration, which has resulted in the formation of phyllosilicates in matrix and in chondrules. The suprising result from Grosnaja is that three different types of phyllosilicates are intimately intergrown. Serpentine is the most abundant phyllosilicate in matrix and occurs as fine-grained packets along grain boundaries and as fracture-fillings and veinlets that cross cut olivine and pyroxene grains. Mixed with the serpentine are packets of fine-grained phyllosilicates with a distinct 1.4-nm basal spacing that is probably a chlorite group mineral. Rare packets of smectite occur as epitaxial intergrowths with olivine, but are not interstratified with serpentine as observed in the CI chondrites. Phyllosilicates in Grosnaja matrix occur with Mg-rich carbonates, fine-grained magnetite, chromite and pentlandite, and poorly-crystalline FeNi- oxide/hydroxides, which stain the matrix a brownish-red color. Some of the rust may be of terrestrial origin (Grosnaja fell in 1861). Although the matrix phyllosilicates are too small to obtain single-phase chemical analyses in the TEM, quantitative EDX analyses suggest that the serpentine contains significant Fe (Mg/Mg + Fe ~0.5). The serpentine/chlorite forms as an alteration product of matrix olivine. Olivine in matrix is equilibrated (Fa(sub)50). The matrix olivines contain numerous planar defects along (100) planes, which results in strong streaking along a* in electron diffraction patterns. These planar defects in matrix olivines are common in other CV chondrites, including Bali [3] and Mokoia [1]. Chondrule mesostasis is extensively altered to coarse-grained Na-saponite that is coherently interstratified with a 1.4-nm phyllosilicate (as shown by selected-area electron diffraction patterns). The 1.4-nm layers occur individually and in groups up to five layers wide. Serpentine has not been observed in chondrules. The Mg/Mg + Fe (atomic) ratio for the saponite is ~0.9, the same as for the host chondrule olivines. The formation of phyllosilicates in Grosnaja was controlled by local bulk compositions. The abundance of Na and Al in chondrule mesostasis stabilized Na-saponite, while in matrix, the high olivine content resulted in formation of serpentine. Grosnaja is unusual for a CV chondrite in that the dominant phyllosilicates in matrix are serpentine and chlorite, whereas smectite is the dominant phyllosilicate for the other altered CV chondrites [3]. This result suggests that alteration conditions were different for Grosnaja relative to the other CV falls. We believe that the occurrence of chlorite in both matrix and chondrules indicates alteration at temperatures higher than those experienced by the other altered CV chondrites. The heat source for the alteration reactions may be related to the thermal event that equilibrated matrix olivines. Acknowledgements: We thank G. Kurat of the Naturhistorisches Museum for samples of Grosnaja. This work was supported by NASA RTOPs 152-17-40-23 and 199-52-11-02. References: [1] Tomeoka K. and Buseck P. R. (1990) GCA, 54, 1745. [2] Keller L. P. and Buseck P. R. (1990) GCA, 54, 2113. [3] Keller L. P. and Thomas K. L. (1991) LPS XXII, 705. [4] McSween H. Y. (1977) GCA, 41, 1777.

Chlorine dioxide water disinfection: a prospective epidemiology study

DOE Office of Scientific and Technical Information (OSTI.GOV)

Michael, G.E.; Miday, R.K.; Bercz, J.P.

An epidemiologic study of 198 persons exposed for 3 months to drinking water disinfected with chlorine dioxide was conducted in a rural village. A control population of 118 nonexposed persons was also studied. Pre-exposure hematologic and serum chemical parameters were compared with test results after 115 days of exposure. Chlorite ion levels in the water averaged approximately 5 ppM during the study period. Statistical analysis (ANOVA) of the data failed to identify any significant exposure-related effects. This study suggests that future evaluations of chlorine dioxide disinfection should be directed toward populations with potentially increased sensitivity to hemolytic agents.

Petrology and sedimentology of the Horlick Formation (Lower Devonian), Ohio Range, Transantarctic Mountains

USGS Publications Warehouse

McCartan, Lucy; Bradshaw, Margaret A.

1987-01-01

The Horlick Formation of Early Devonian age is as thick as 50 m and consists of subhorizontal, interbedded subarkosic sandstone and chloritic shale and mudstone. The Horlick overlies an erosion surface cut into Ordovician granitic rocks and is, in turn, overlain by Carboniferous and Permian glacial and periglacial deposits. Textures, sedimentary structures, and ubiquitous marine body fossils and animal traces suggest that the Horlick was deposited on a shallow shelf having moderate wave energy and a moderate tidal range. The source terrane probably lay to the north, and longshore transport was toward the west.

Spontaneous Symmetry Breaking Turing-Type Pattern Formation in a Confined Dictyostelium Cell Mass

NASA Astrophysics Data System (ADS)

Sawai, Satoshi; Maeda, Yasuo; Sawada, Yasuji

2000-09-01

We have discovered a new type of patterning which occurs in a two-dimensionally confined cell mass of the cellular slime mold Dictyostelium discoideum. Besides the longitudinal structure reported earlier, we observed a spontaneous symmetry breaking spot pattern whose wavelength shows similar strain dependency to that of the longitudinal pattern. We propose that these structures are due to a reaction-diffusion Turing instability similar to the one which has been exemplified by CIMA (chlorite-iodide-malonic acid) reaction. The present finding may exhibit the first biochemical Turing structure in a developmental system with a controllable boundary condition.

Interpretation of 40Ar/39Ar Age-spectra in Low-grade Polymetamorphic Rocks: The Importance of Petrologic constraints

NASA Astrophysics Data System (ADS)

Kunk, M. J.

2007-12-01

40Ar/39Ar age-spectra of white micas from low-grade polymetamorphic terranes can be difficult to interpret, because these low-grade rocks frequently have multiple generations of cleavage-forming white mica that grew at temperatures below their closure for diffusion of argon (~350°C). Under such conditions, each generation of cleavage-forming white mica will retain its original growth age. In addition, rocks from metamorphic terranes can also contain populations of detrital and diagenetic white micas which also have distinct ages associated with them. A final complication, frequently found in these low-grade polymetamorphic samples is the presence of inseparable, intergrown chlorite and the problems with associated 39Ar recoil during irradiation of the samples, prior to sample analysis. The shapes of 40Ar/39Ar age spectra of white micas separated from such samples are frequently complex and are quite variable in shape. Some age spectra show a steady increase in age with increase in the temperature of release, while others have sigmoidal or saddle-shaped patterns. The age of most of the steps in such age spectra are mixtures of the various age populations of white mica in the sample, and as such are geologically meaningless. Nonetheless, useful constraints on the ages of at least some events recorded in these complex low-grade polymetamorphic rocks can be discerned with the help of petrographic observations, and by placing the results in a spatial context to test for reproducibility and/or the occurrence of meaningful patterns. If no chlorite is present and the sample contains no detrital white mica, an estimate of the maximum age of the youngest component and the minimum age of the oldest cleavage forming white mica populations can frequently be discerned. If the sample contains detrital white mica, a minimum age for its cooling or crystallization can be estimated. The presence of a small amount of intimately intergrown chlorite masks the age of the youngest white mica population, but the minimum age of the oldest generation of white mica may still be estimated. Samples from the Blue Ridge anticlinorium in northern VA indicate cleavage formation during both the Devonian and the Pennsylvanian. Similar, but somewhat more complex samples from the Potomac terrane in the eastern Piedmont of northern VA and MD indicate discrete tectonothermal events in the Ordovician, Silurian, and Pennsylvanian, while samples from the Westminster terrane in the westerm Piedmont of MD suggest cleavage formation in the middle Silurian, the Devonian and the Pennsylvanian. While the results are not of high precision, they are very useful at the orogenic level.

Clay minerals behaviour in thin sandy clay-rich lacustrine turbidites (Lake Hazar, Turkey)

NASA Astrophysics Data System (ADS)

El Ouahabi, Meriam; Hubert-Ferrari, Aurelia; Lamair, Laura; Hage, Sophie

2017-04-01

Turbidites have been extensively studied in many different areas using cores or outcrop, which represent only an integrated snapshot of a dynamic evolving flow. Laboratory experiments provide the missing relationships between the flow characteristics and their deposits. In particular, flume experiments emphasize that the presence of clay plays a key role in turbidity current dynamics. Clay fraction, in small amount, provides cohesive strength to sediment mixtures and can damp turbulence. However, the degree of flocculation is dependent on factors such as the amount and size of clay particles, the surface of clay particles, chemistry and pH conditions in which the clay particles are dispersed. The present study focuses on thin clayey sand turbidites found in Lake Hazar (Turkey) occurring in stacked thin beds. Depositional processes and sources have been previously studied and three types were deciphered, including laminar flows dominated by cohesion, transitional, and turbulence flow regimes (Hage et al., in revision). For the purpose of determine the clay behavior in the three flow regimes, clay mineralogical, geochemical measurements on the cores allow characterising the turbidites. SEM observations provide further information regarding the morphology of clay minerals and other clasts. The study is particularly relevant given the highly alkaline and saline water of the Hazar Lake. Clay minerals in Hazar Lake sediments include kaolinite (1:1-type), illite and chlorite (2:1-type). Hazar lake water is alkaline having pH around 9.3, in such alkaline environment, a cation-exchange reaction takes place. Furthermore, in saline water (16‰), salts can act as a shield and decrease the repulsive forces between clay particle surfaces. So, pH and salt content jointly impact the behaviour of clays differently. Since the Al-faces of clay structures have a negative charge in basic solutions. At high pH, all kaolinite surfaces become negative-charged, and then kaolinite particles are dispersed, and the suspension is stabilized supported by our SEM observations. In alkaline water, kaolinite reveals a lower degree of consolidation. While, alkaline water has no measurable effect on illite and chlorite surface properties due to the absence of modifications in charge. Illite and chlorite form with other clasts clusters or aggregate structures in suspension when the particle interactions are dominated by attractive energies were formed. The aggregate structure plays a major part in the flow behavior of clay suspensions. Flocs will immobilize the suspending medium, and give rise to increasing viscosity and yield strength of the suspension. S. Hage, A. Hubert-Ferrari, L. Lamair, U. Avşar, M. El Ouahabi, M. Van Daele, F. Boulvain, M.A. Bahri, A. Seret, Al. Plenevaux. Flow dynamics at the origin of thin sandy clay-rich lacustrine turbidites: Examples from Lake Hazar, Turkey, submitted to Sedimentology, in revision.

Rodingite in Layered Gabbro of the Leka Ophiolite Complex, North-Central Caledonides of Norway

NASA Astrophysics Data System (ADS)

Prestvik, T.; Austrheim, H.

2006-12-01

Both the ultramafic (mantle) and the layered ultramafic to gabbroic (crustal) sequences of the Cambrian (497 Ma) Leka ophiolite are characterized by extensive serpentinization. Rodingite, containing grossular garnet, clinopyroxene, clinozoisite, prehnite, chlorite and preiswerkite, which has been found in the lowermost plagioclase-rich layers of the gabbro sequence seems to represent an unusual (new?) mode of rodingite occurrence compared to the more common rodingitized basaltic dikes described from many ultramafic complexes worldwide. The 5 to 15 cm wide rodingitized plagioclase layers, that alternate with less altered layers of wehrlite, clinopyroxenite, and websterite, are located c. 10 m away from a 10 m wide layer of serpentinized dunite. The whole sequence is cut by numerous fractures oriented almost perpendicular to the layering, and rodingite occurs where the fractures transect the plagioclase layers. In the adjacent lithologies, the fractures can be followed as thin veins filled with grossular, clinopyroxene, amphibole, epidote, and chlorite. These fractures were most likely channelways for the rodingite-forming fluids. Gresen analysis, assuming constant volume, shows that the rodingite formed from the plagioclase-rich layers by addition of c. 22 g of CaO, 6 g of FeO and SiO2 and removal of 10 g of Al2O3 and all (2 g) of Na2O per 100 g of protolith. Microtextures show chlorite and serpentine pseudomorphs after primary clinopyroxene, demonstrating that the alteration took place at constant volume. This reaction is the most likely Ca source for the rodingitization, possibly in addition to the serpentinization of olivine in the dunite layers. Furthermore, Ca-enriched and Al2O3- depleted clinopyroxene of the rodingite - compared to the primary clinopyroxene of the layered sequence - attest to the mobil nature of these elements. While both the protolith and the rodingite are almost K2O-free, one of the plagioclase-rich layers has K2O in the 1.1 to 1.4% range for several meters along strike and has abundant secondary phlogopite. The source for K is not easily accounted for and may suggest large scale transport. LA-ICP-MS analysis of trace elements in grossular garnet shows a strongly LREE depleted pattern with a considerable (10x) positive Eu anomaly. We interpret this as evidence for reduced conditions during formation of the rodingite (or that the garnet inherited the Eu anomaly from primary plagioclase). This first description of rodingite at Leka indicates that serpentinization and rodingitization were related and most likely took place as part of a large scale Cambrian hydrothermal system associated with an oceanic rift. It further implies that the hydrothermal alteration affected rocks at sub-Moho level.

The significance of visitors' pressure for soil status in an urban park in Tel-Aviv

NASA Astrophysics Data System (ADS)

Zhevelev, Helena; Sarah, Pariente; Oz, Atar

2010-05-01

A park is one of the most important elements of sustainable development and optimization of the urban environment. The equilibrium within the complex of natural and anthropogenic factors defines the status of a park's ecosystem. The seasonal dynamics and spatial variations of soil properties in areas under differing levels of visitors' pressure were studied in a park in Tel-Aviv. Soil was sampled twice a year, in wet (March) and dry (July) seasons, from three types of areas, subjected to differing levels of visitors' pressure: high, low and none (control). In each type of area samples were taken from two depths (0-2 cm and 5-10 cm), at 14-39 points. In total, 268 soil samples were taken. Before the soil sampling, penetration depth was determined at each point. In addition, the numbers of barbecue fires in each of the three areas were counted. Gravimetric soil moisture, organic matter, pH, electrical conductivity, and soluble ions were measured in 1:1 water extraction. Penetration depth and electrical conductivity, and organic matter, sodium, potassium and chlorite contents differed under differing levels of visitors' pressure, whereas soil moisture, pH and calcium content exhibited only minor differences. Soil moisture, electrical conductivity, and magnesium and chlorite contents exhibited strong seasonal changes, whereas the organic matter, potassium and pH levels were unaffected by seasonal dynamics. Calcium, organic matter, magnesium and chlorite contents, and electrical conductivity were significantly affected by the depth of soil sampling, whereas pH was not so affected. The seasonal changes in soil properties in the area subjected to high visitors' pressure were higher than in the one under low visitors' pressure. In most cases, visitors' pressure led to increases in variance and coefficient of variation. Different soil properties were differently affected by visitors' pressure, seasonal dynamics and soil depth. The surface of the soil was more sensitive to both seasonal dynamics and visitors' pressure, than the deeper layer. Visitors' pressure increased seasonal changes in the studied soil properties, and also increased the spatial heterogeneity of the soil. The differences in organic matter, electrical conductivity and soluble ions among the areas under differing visitors' pressure are attributed to anthropogenic additions, which accompanied the recreational activities in the urban parks: remnants of barbecue fires and meals, and excreta of urban animals. Addition of urban dust, enriched in CaCO3, minimized the effect of visitors' pressure on soil calcium content. All the above anthropogenic additions enhance the differentiation in soil layers. The notable effect of visitors' pressure on variations in soil properties highlighted its high significance for urban parks.

Ubiquity and Diversity of Dissimilatory (Per)chlorate-Reducing Bacteria

PubMed Central

Coates, John D.; Michaelidou, Urania; Bruce, Royce A.; O’Connor, Susan M.; Crespi, Jill N.; Achenbach, Laurie A.

1999-01-01

Environmental contamination with compounds containing oxyanions of chlorine, such as perchlorate or chlorate [(per)chlorate] or chlorine dioxide, has been a constantly growing problem over the last 100 years. Although the fact that microbes reduce these compounds has been recognized for more than 50 years, only six organisms which can obtain energy for growth by this metabolic process have been described. As part of a study to investigate the diversity and ubiquity of microorganisms involved in the microbial reduction of (per)chlorate, we enumerated the (per)chlorate-reducing bacteria (ClRB) in very diverse environments, including pristine and hydrocarbon-contaminated soils, aquatic sediments, paper mill waste sludges, and farm animal waste lagoons. In all of the environments tested, the acetate-oxidizing ClRB represented a significant population, whose size ranged from 2.31 × 103 to 2.4 × 106 cells per g of sample. In addition, we isolated 13 ClRB from these environments. All of these organisms could grow anaerobically by coupling complete oxidation of acetate to reduction of (per)chlorate. Chloride was the sole end product of this reductive metabolism. All of the isolates could also use oxygen as a sole electron acceptor, and most, but not all, could use nitrate. The alternative electron donors included simple volatile fatty acids, such as propionate, butyrate, or valerate, as well as simple organic acids, such as lactate or pyruvate. Oxidized-minus-reduced difference spectra of washed whole-cell suspensions of the isolates had absorbance maxima close to 425, 525, and 550 nm, which are characteristic of type c cytochromes. In addition, washed cell suspensions of all of the ClRB isolates could dismutate chlorite, an intermediate in the reductive metabolism of (per)chlorate, into chloride and molecular oxygen. Chlorite dismutation was a result of the activity of a single enzyme which in pure form had a specific activity of approximately 1,928 μmol of chlorite per mg of protein per min. Analyses of the 16S ribosomal DNA sequences of the organisms indicated that they all belonged to the alpha, beta, or gamma subclass of the Proteobacteria. Several were closely related to members of previously described genera that are not recognized for the ability to reduce (per)chlorate, such as the genera Pseudomonas and Azospirllum. However, many were not closely related to any previously described organism and represented new genera within the Proteobacteria. The results of this study significantly increase the limited number of microbial isolates that are known to be capable of dissimilatory (per)chlorate reduction and demonstrate the hitherto unrecognized phylogenetic diversity and ubiquity of the microorganisms that exhibit this type of metabolism. PMID:10583970

Hydrothermal alteration and mass exchange in the hornblende latite porphyry, Rico, Colorado

USGS Publications Warehouse

Larson, P.B.; Cunningham, C.G.; Naeser, C.W.

1994-01-01

The Rico paleothermal anomaly, southwestern Colorado, records the effects of a large hydrothermal system that was active at 4 Ma. This hydrothermal system produced the deep Silver Creek stockwork Mo deposit, which formed above the anomaly's heat source, and shallower base and precious-metal vein and replacement deposits. A 65 Ma hornblende latite porphyry is present as widespread sills throughout the area and provided a homogenous material that recorded the effects of the hydrothermal system up to 8 km from the center. Hydrothermal alteration in the latite can be divided into a proximal facies which consists of two assemblages, quartz-illite-calcite and chlorite-epidote, and a distal facies which consists of a distinct propylitic assemblage. Temperatures were gradational vertically and laterally in the anomaly, and decreased away from the centra heat source. A convective hydrothermal plume, 3 km wide and at least 2 km high, was present above the stock-work molybdenum deposit and consisted of upwelling, high-temperature fluids that produced the proximal alteration facies. Distal facies alteration was produced by shallower cooler fluids. The most important shallow base and precious-metal vein deposits in the Rico district are at or close to the boundary of the thermal plume. Latite within the plume had a large loss of Na2O, large addition of CaO, and variable SiO2 exchante. Distal propylitized latite samples lost small amounts of Na2O and CaO and exchanged minor variable amounts of SiO2. The edge of the plume is marked by steep Na2O exchange gradients. Na2O exchange throughout the paleothermal anomaly was controlled by the reaction of the albite components in primary plagioclase and alkali feldspars. Initial feldspar alteration in the distal facies was dominated by reaction of the plagioclase, and the initial molar ratio of reactants (alkali feldspar albite component to plagioclase albite component) was 0.35. This ratio of the moles of plagioclase to alkali feldspar albite components that reacted evolved to 0.92 as the reaction progressed. Much of the alkali feldspar albite component in the proximal facies reacted while the, primary plagioclase was still unreacted, but the ratio for these assemblages increased to 1.51 when the plagioclase entered the reaction paragenesis. Plagioclase reaction during distal propylitic alteration resulted in pseudomorphic albite mixed with illite and a loss of Na2O. CaO is lost in the distal facies as hornblende reacts to chlorite, although some calcium may be fixed in calcite. CaO is added to the proximal facies as the quantity of chlorite replacing hornblende increases and epidote and calcite are produced. ?? 1994 Springer-Verlag.

The Marianas-San Marcos vein system: characteristics of a shallow low sulfidation epithermal Au-Ag deposit in the Cerro Negro district, Deseado Massif, Patagonia, Argentina

NASA Astrophysics Data System (ADS)

Vidal, Conrado Permuy; Guido, Diego M.; Jovic, Sebastián M.; Bodnar, Robert J.; Moncada, Daniel; Melgarejo, Joan Carles; Hames, Willis

2016-08-01

The Cerro Negro district, within the Argentinian Deseado Massif province, has become one of the most significant recent epithermal discoveries, with estimated reserves plus resources of ˜6.7 Moz Au equivalent. The Marianas-San Marcos vein system contains about 70 % of the Au-Ag resources in the district. Mineralization consists of Upper Jurassic (155 Ma) epithermal Au- and Ag-rich veins of low to intermediate sulfidation style, hosted in and genetically related to Jurassic intermediate composition volcanic rocks (159-156 Ma). Veins have a complex infill history, represented by ten stages with clear crosscutting relationships that can be summarized in four main episodes: a low volume, metal-rich initial episode (E1), an extended banded quartz episode with minor mineralization (E2), a barren waning stage episode (E3), and a silver-rich late tectonic-hydrothermal episode (E4). The first three episodes are interpreted to have formed at the same time and probably from fluids of similar composition: a 290-230 °C fluid dominated by meteoric and volcanic waters (-3‰ to -0‰ δ18Owater), with <3 % NaCl equivalent salinity and with a magmatic source of sulfur (-1 to -2 ‰ δ34Swater). Metal was mainly precipitated at the beginning of vein formation (episode 1) due to a combination of boiling at ˜600 to 800 m below the paleowater table, and associated mixing/cooling processes, as evidenced by sulfide-rich bands showing crustiform-colloform quartz, adularia, and chlorite-smectite banding. During episodes 2 and 3, metal contents progressively decrease during continuing boiling conditions, and veins were filled by quartz and calcite during waning stages of the hydrothermal system, and the influx of bicarbonate waters (-6 to -8.5 ‰ δ18Owater). Hydrothermal alteration is characterized by proximal illite, adularia, and silica zone with chlorite and minor epidote, intermediate interlayered illite-smectite and a distal chlorite halo. This assemblage is in agreement with measured fluid inclusion temperatures. A striking aspect of the Marianas-San Marcos vein system is that the high-grade/high-temperature veins are partially covered by breccia and volcaniclastic deposits of acidic composition, and are spatially associated with hot spring-related deposits and an advanced argillic alteration blanket. A telescoped model is therefore proposed for the Marianas-San Marcos area, where deeper veins were uplifted and eroded, and then partially covered by non-explosive, post-mineral rhyolitic domes and reworked volcaniclastic deposits, together with shallow geothermal features. The last tectonic-hydrothermal mineralization episode (E4), interpreted to have formed at lower temperatures, could be related to this late tectonic and hydrothermal activity.

Thermodynamic modeling of phase relations and metasomatism in shear zones

NASA Astrophysics Data System (ADS)

Goncalves, P.; Oliot, E.; Marquer, D.

2009-04-01

Ductile shear zones have been recognized for a long time as privileged sites of intense fluid-rock interactions in the crust. In most cases they induce focused changes in mineralogy and bulk chemical composition (metasomatism) which in turn may control the deformation and fluid-migration processes. Therefore understanding these processes requires in a first step to be able to model phase relations in such open system. In this contribution, emphasizes in placed on metasomatic aspects of the problem. Indeed , in many ductile shear zones reported in metagranites, deformation and fluid-rock interactions are associated with gain in MgO and losses of CaO and Na2O (K2O is also a mobile component but it can be either gained or lost). Although the mineralogical consequences of this so-called Mg-metasomatism are well-documented (replacement of K-feldspar into phengite, breakdown of plagioclase into ab + ep, crystallization of chlorite), the origin of this coupled mass-transfer is still unknown. We have performed a forward modeling of phase relationships using petrogenetic grids and pseudosections that consider variations in chemical potential (μ) of the mobile elements (MgO, CaO, Na2O). Chemical potential gradients being the driving force of mass transfer, μ-μ diagrams are the most appropriate diagrams to model open systems where fluid-rock interactions are prominent. Chemical potential diagrams are equivalent to activity diagrams but our approach differs from previous work because (1) solid solutions are taken into account (2) phase relations are modeled in a more realistic chemical system (Na2O-CaO-K2O-FeO-MgO-Al2O3-SiO2-H2O) and (3) the use of pseudosections allows to predict changes of the mineralogy (modes, composition) for the specific bulk composition studied. A particular attention is paid to the relationships between component concentrations and chemical potentials, which is not obvious in multi-component system. The studied shear zone is located in the Grimsel granodiorite (Swiss Alps). Fourteen samples have been taken along a 80 meter-wide strain gradient from the undeformed granodiorite protolith to the ultramylonitic zone. The metastable magmatic assemblage consists of oligoclase (50 vol%), quartz ( 20 vol%), K-feldspar (17 vol%), and biotite (13 %). With increasing strain, K-feldspar and oligoclase rapidly disappear to produce albite and epidote porphyroblast (up to 45 and 5 vol% respectively) with phengite in shear planes (15 vol%). In the mylonite and ultramylonite, magmatic phases have been completely recrystallized and the metamorphic albite volume decreases down to 25 vol% whereas phengite constitutes up to 30 vol% of the rock. Epidote is absent in the ultramylonite. In localized shear bands, the metamorphic assemblage consists of phengite, chlorite, biotite and quartz. Mass balance calculations show that the ultramylonite is enriched in MgO (up to 130%) while CaO and Na2O are remove (80% and 45% respectively). However, mass transfer is even stronger in the chlorite-bearing shear bands, where CaO and Na2O have been completely leached out. Chemical potential pseudosections are constructed using the bulk composition of the unaltered granodiorite, with K2O, FeO, Al2O3 and SiO2 content remaining constant. Deformation occurred under water-saturated conditions at 6 kbar and 450°C. MgO, CaO and Na2O are considered as "perfectly mobile" components and therefore their chemical potentials, which is fixed by the externally-derived fluid, control the stability of the phases. μMgO vs μCaO and μMgO vs μNa2O diagrams, show that the breakdown of a Kf-ab-ep assemblage into phengite and the subsequent crystallization of chlorite require the introduction of a fluid with a μCaO and μNa2O significantly lower than in the unaltered metamorphic assemblage (Kf-ab-ep-Kf-Bio-q). Equalizing the chemical potential gradient of CaO and Na2O, established between the fluid and the metamorphic assemblage, is achieved by the complete removal of CaO and Na2O. The most striking result is that chemical potential diagram predicts that the loss of CaO and Na2O and the crystallization of chlorite-bearing assemblage at the expense of Kf-ep-ab imply a gain of MgO to reach equilibrium: "Mg-metasomatism" is therefore controlled and induced by the metamorphic assemblage. Finally fluid-rock interactions and mass transfer result in an increase in phyllosilicates in the shear zone from 13 to 32 vol%, which should strongly enhance the strain localization process. To conclude, our approach allows to predict and to quantify the mineralogical changes induced by fluid-rock interactions in a shear zone for any bulk composition or P-T composition.

Chlorate origin and fate in shallow groundwater below agricultural landscapes.

PubMed

Mastrocicco, Micòl; Di Giuseppe, Dario; Vincenzi, Fabio; Colombani, Nicolò; Castaldelli, Giuseppe

2017-12-01

In agricultural lowland landscapes, intensive agricultural is accompanied by a wide use of agrochemical application, like pesticides and fertilizers. The latter often causes serious environmental threats such as N compounds leaching and surface water eutrophication; additionally, since perchlorate can be present as impurities in many fertilizers, the potential presence of perchlorates and their by-products like chlorates and chlorites in shallow groundwater could be a reason of concern. In this light, the present manuscript reports the first temporal and spatial variation of chlorates, chlorites and major anions concentrations in the shallow unconfined aquifer belonging to Ferrara province (in the Po River plain). The study was made in 56 different locations to obtain insight on groundwater chemical composition and its sediment matrix interactions. During the monitoring period from 2010 to 2011, in June 2011 a nonpoint pollution of chlorates was found in the shallow unconfined aquifer belonging to Ferrara province. Detected chlorates concentrations ranged between 0.01 and 38 mg/l with an average value of 2.9 mg/l. Chlorates were found in 49 wells out of 56 and in all types of lithology constituting the shallow aquifer. Chlorates concentrations appeared to be linked to NO 3 - , volatile fatty acids (VFA) and oxygen reduction potential (ORP) variations. Chlorates behaviour was related to the biodegradation of perchlorates, since perchlorates are favourable electron acceptors for the oxidation of labile dissolved organic carbon (DOC) in groundwater. Further studies must take into consideration to monitor ClO 4 - in pore waters and groundwater to better elucidate the mass flux of ClO 4 - in shallow aquifers belonging to agricultural landscapes. Copyright © 2017 Elsevier Ltd. All rights reserved.

Formation of albitite-hosted uranium within IOCG systems: the Southern Breccia, Great Bear magmatic zone, Northwest Territories, Canada

NASA Astrophysics Data System (ADS)

Montreuil, Jean-François; Corriveau, Louise; Potter, Eric G.

2015-03-01

Uranium and polymetallic U mineralization hosted within brecciated albitites occurs one kilometer south of the magnetite-rich Au-Co-Bi-Cu NICO deposit in the southern Great Bear magmatic zone (GBMZ), Canada. Concentrations up to 1 wt% U are distributed throughout a 3 by 0.5 km albitization corridor defined as the Southern Breccia zone. Two distinct U mineralization events are observed. Primary uraninite precipitated with or without pyrite-chalcopyrite ± molybdenite within magnetite-ilmenite-biotite-K-feldspar-altered breccias during high-temperature potassic-iron alteration. Subsequently, pitchblende precipitated in earthy hematite-specular hematite-chlorite veins associated with a low-temperature iron-magnesium alteration. The uraninite-bearing mineralization postdates sodic (albite) and more localized high-temperature potassic-iron (biotite-magnetite ± K-feldspar) alteration yet predates potassic (K-feldspar), boron (tourmaline) and potassic-iron-magnesium (hematite ± K-feldspar ± chlorite) alteration. The Southern Breccia zone shares attributes of the Valhalla (Australia) and Lagoa Real (Brazil) albitite-hosted U deposits but contains greater iron oxide contents and lower contents of riebeckite and carbonates. Potassium, Ni, and Th are also enriched whereas Zr and Sr are depleted with respect to the aforementioned albitite-hosted U deposits. Field relationships, geochemical signatures and available U-Pb dates on pre-, syn- and post-mineralization intrusions place the development of the Southern Breccia and the NICO deposit as part of a single iron oxide alkali-altered (IOAA) system. In addition, this case example illustrates that albitite-hosted U deposits can form in albitization zones that predate base and precious metal ore zones in a single IOAA system and become traps for U and multiple metals once the tectonic regime favors fluid mixing and oxidation-reduction reactions.

Role of upwelling hydrothermal fluids in the development of alteration patterns at fast spreading ridges: Evidence from the sheeted dike complex at Pito Deep

NASA Astrophysics Data System (ADS)

Heft, Kerri L.; Gillis, Kathryn M.; Pollock, Megan A.; Karson, Jeffery A.; Klein, Emily M.

2008-05-01

Alteration of sheeted dikes exposed along submarine escarpments at the Pito Deep Rift (NE edge of the Easter microplate) provides constraints on the crustal component of axial hydrothermal systems at fast spreading mid-ocean ridges. Samples from vertical transects through the upper crust constrain the temporal and spatial scales of hydrothermal fluid flow and fluid-rock reaction. The dikes are relatively fresh (average extent of alteration is 27%), with the extent of alteration ranging from 0 to >80%. Alteration is heterogeneous on scales of tens to hundreds of meters and displays few systematic spatial trends. Background alteration is amphibole-dominated, with chlorite-rich dikes sporadically distributed throughout the dike complex, indicating that peak temperatures ranged from <300°C to >450°C and did not vary systematically with depth. Dikes locally show substantial metal mobility, with Zn and Cu depletion and Mn enrichment. Amphibole and chlorite fill fractures throughout the dike complex, whereas quartz-filled fractures and faults are only locally present. Regional variability in alteration characteristics is found on a scale of <1-2 km, illustrating the diversity of fluid-rock interaction that can be expected in fast spreading crust. We propose that much of the alteration in sheeted dike complexes develops within broad, hot upwelling zones, as the inferred conditions of alteration cannot be achieved in downwelling zones, particularly in the shallow dikes. Migration of circulating cells along rides axes and local evolution of fluid compositions produce sections of the upper crust with a distinctive character of alteration, on a scale of <1-2 km and <5-20 ka.

Lithology, petrography and Cu occurrence of the Neoproterozoic glacial Mwale Formation at the Shanika syncline (Tenke Fungurume, Congo Copperbelt; Democratic Republic of Congo)

NASA Astrophysics Data System (ADS)

Mambwe, Pascal; Milan, Luke; Batumike, Jacques; Lavoie, Sébastien; Jébrak, Michel; Kipata, Louis; Chabu, Mumba; Mulongo, Sonya; Lubala, Toto; Delvaux, Damien; Muchez, Philippe

2017-05-01

The Mwale Formation that constitutes the base of the Nguba Group in the Neoproterozoic Katanga Supergroup has recently attracted renewed interest for copper mineral exploration. We present new field observations combined with detailed logging and petrography of MWAS0001 drill hole at Shanika syncline in the Tenke Fungurume Mining District. Our study has enabled us to subdivide the Mwale Formation into 7 distinct sequences. This succession is host to glaciogenic, glaciomarine, glaciofluvial and glaciolacustrine deposits. Glaciomarine beds are typically a deposit by debris flow in deep water marine environment, induced by basin wide tectonics and glaciation influence. Glaciofluvial beds were deposited in shallow water, fluvial deltaic environment. The glaciolacustrine environment is indicated by dropstones occurring in the laminated mudstone and rhythmites with dispersed clasts observed in the siltstone and conglomerate. These beds are interlayered within the glaciogenic beds, and are characterised by variable clast composition (felsic, mafic and metamorphic). The clasts are very poorly sorted, angular, rounded to moderately rounded, faceted or striated, and supported in a sandy argillaceous or mud matrix. Two main episodes of sulphide mineralisation are distinguished in the Mwale Formation. The diagenetic episode consists of disseminated euhedral and framboidal pyrites. The hydrothermal episode is associated with Mg-metasomatism and characterised by low grade copper mineralisation that occurs (i) in veins filled with carbonate-chlorite and carbonate-quartz-chlorite-Cu sulphides, such as chalcocite, chalcopyrite and bornite, and (ii) as disseminated sulphides within the host rock. This second episode is late to post-orogenic and can be correlated with late brittle tectonics within the Lufilian arc. The other alteration types include silicification and potassic alteration; however, these alterations are not associated with mineralisation.

Geological and geochemical studies of the Shujiadian porphyry Cu deposit, Anhui Province, Eastern China: Implications for ore genesis

NASA Astrophysics Data System (ADS)

Wang, Shiwei; Zhou, Taofa; Yuan, Feng; Fan, Yu; White, Noel C.; Lin, Fengjie

2015-05-01

Most porphyry deposits in the world occur in magmatic arc settings and are related to subduction of oceanic plates. A small proportion of porphyry deposits occur in intracontinental settings, however they are still poorly understood. Shujiadian, a newly-discovered porphyry Cu deposit, is located in the Middle-Lower Yangtze River Valley metallogenic belt and belongs to the intracontinental class. The deposit has classic alteration zones defined by a core of potassic alteration and local Ca-silicate alteration, which is overprinted by a feldspar-destructive alteration zone and cut by veins containing epidote and chlorite. Wallrocks of the deposit are unreactive quartz-rich sedimentary rocks. Three main paragenetic stages have been recognized based on petrographic observations; silicate stage, quartz-sulfide stage, and sulfide-carbonate stage. Quartz + pyrite + chalcopyrite ± molybdenite veins, and quartz + chalcopyrite + pyrite veins of the quartz-sulfide stage contribute most of the copper, and chalcopyrite + chlorite ± pyrite ± pyrrhotite ± quartz ± illite veins of the sulfide-carbonate stage also contribute part of the copper; all the mineralized veins are associated with feldspar-destructive alteration. Investigations on the fluid inclusions in Shujiadian indicate that the ore-forming fluids had four evolutionary episodes: immiscibility and overpressure in the silicate stage, boiling in the quartz-sulfide stage and mixing with meteoric water in the sulfide-carbonate stage. Sulfur and strontium isotope studies suggest that ore metals were mainly derived from magmatic-hydrothermal fluids, and combined with our study of fluid inclusions, we infer that decompression, changes in oxygen fugacity and sulfur content were the main factors that caused Cu precipitation. Compared with porphyry deposits in magmatic arc settings, there are some differences in the ore-bearing rock, alteration, and the composition of ore-forming fluids.

Mineralogical and geochemical features of the alteration processes of magmatic ores in the Beni Bousera ultramafic massif (north Morocco)

NASA Astrophysics Data System (ADS)

Hajjar, Zaineb; Gervilla, Fernando; Essaifi, Abderrahim; Wafik, Amina

2017-08-01

The Beni Bousera ultramafic massif (Internal Rif, Morocco) is characterized by the presence of two types of small-scale magmatic mineralizations (i) a mineralization consisting mainly of chromite and Ni arsenides associated to orthopyroxene and cordierite (Cr-Ni ores), and (ii) a mineralization mainly composed of magmatic Fe-Ni-Cu sulfides containing variable amounts of graphite and chromite associated to phlogopite, clinopyroxène and plagioclase (S-G ores). Theses ores underwent High-T (450-550 °C) and Low-T (150-300 °C) alteration processes. The High-T alteration processes are tentatively related to intrusion of leucogranite dykes. They are preserved in the Galaros Cr-Ni ore deposit where nickeline is partly dissolved and transformed to maucherite, and orthopyroxene alters to phlogopite. Ni and Co were mobilized to the fluid phase, rising up their availability and promoting their diffusion into chromite and phlogopite, which have significantly higher contents in Ni and Co in phlogopite-rich ores than in orthopyroxene- and nickeline-rich ones. The Low-T alteration processes are related to serpentinization/weathering spatially associated with a regional shear zone. They affected both the Cr-Ni and S-G ores. In the Cr-Ni ores, Ni-arsenides were completely leached out while chromite is fractured within a matrix of chlorite, vermiculite and Ni-rich serpentine. In S-G ores, the silicates were altered into amphibole, Fe-rich chlorite and pectolite in clinopyroxene- and plagioclase-bearing ores while sulfides were completely leached out in phlogopite-bearing ores where iron oxides and hydroxides, and Fe-rich vermiculite were deposited. Chromite composition is not affected by the Low-T alteration processes.

Clay mineralogy of the ocean sediments from the Wilkes Land margin, east Antarctica: implications on the paleoclimate, provenance and sediment dispersal pattern

NASA Astrophysics Data System (ADS)

Verma, Kamlesh; Bhattacharya, Sanjeeb; Biswas, P.; Shrivastava, Prakash K.; Pandey, Mayuri; Pant, N. C.

2014-11-01

Core U1359 collected from the continental rise off Wilkes Land, east Antarctica, is analyzed for the clay mineralogy and carbon content. The temporal variation of the clay mineralogical data shows a dominance of illite with chlorite, smectite and kaolinite in decreasing concentration. Clay mineral illite is negatively correlated with smectite which shows enrichment during 6.2-6.8, 5.5-5.8, 4.5 and 2.5 Ma. The mineralogical analyses on the silt size fraction (2-53 μm) of some selected samples were also carried out. The combined result of both the size fractions shows the presence of chlorite and illite in both size fractions, smectite and kaolinite only in clay size fraction (<2 μm) and similarity in the crystallinity and chemistry of illite in both fractions. Similar nature of illite in both fractions suggests negligible role of sorting probably due to the deposition from the waxing ice sheet. During times of ice growth, nearby cratonic east Antarctica shield provided biotite-rich sediments to the depositional site. On the other hand, the presence of smectite, only in the clay size fraction, suggests the effective role of sorting probably due to the deposition from distal source in ice retreat condition. During times of ice retreat, smectite-rich sediment derived from Ross Orogen is transported to the core site through surface or bottom water currents. Poor crystallinity of illite due to degradation further corroborates the ice retreat condition. The ice sheet proximal sediments of U1359 show that in the eastern part of Wilkes Land, the `warming' was initiated during late Miocene.

Distributions of clay minerals in surface sediments of the middle Bay of Bengal: Source and transport pattern

NASA Astrophysics Data System (ADS)

Li, Jingrui; Liu, Shengfa; Shi, Xuefa; Feng, Xiuli; Fang, Xisheng; Cao, Peng; Sun, Xingquan; Wenxing, Ye; Khokiattiwong, Somkiat; Kornkanitnan, Narumol

2017-08-01

The clay mineral contents in 110 surface sediment samples collected from the middle of the Bay of Bengal were analyzed by X-ray diffraction (XRD) to investigate the provenance and transport patterns. The illite content was highest, followed by chlorite, kaolinite and then smectite, with average weight percent distributions of 52%, 22%, 14% and 12%, respectively. Illite and chlorite had similar distribution pattern, with higher contents in the northern and central areas and lower contents in the southern area, whereas smectite showed the opposite distribution pattern. Kaolinite show no obvious higher or lower areas and the southern ;belt; was one of the highest content areas. Based on the spatial distribution characteristics and cluster analysis results, the study area can be classified into two provinces. Province I covers the southwestern area and contains high concentrations of illite and smectite sediments. Province II covers most sites and is also characterized by high concentrations of illite, but the weight percent of smectite is only half of that of province I. According to a quantitative estimate using end-member clay minerals contents, the relative contributions from the Himalayan source and the Indian source are 63% and 37% on average, respectively. Integrative analysis indicates that the hydrodynamic environment in the study area, especially the turbidity and surface monsoonal circulation, plays an important role in the spatial distribution and dispersal of the clay fraction in the sediments. The sediments in province I are mainly from the Indian source transported by the East Indian Coastal Current (EICC) and the surface monsoon circulation with minor contributions from the Himalayan source while the sediments in province II are mainly from the Himalayan source transported by turbidity and surface monsoonal circulation with little contribution from Indian river materials.

Continental weathering as a driver of Late Cretaceous cooling: new insights from clay mineralogy of Campanian sediments from the southern Tethyan margin to the Boreal realm

NASA Astrophysics Data System (ADS)

Chenot, Elise; Deconinck, Jean-François; Pucéat, Emmanuelle; Pellenard, Pierre; Guiraud, Michel; Jaubert, Maxime; Jarvis, Ian; Thibault, Nicolas; Cocquerez, Théophile; Bruneau, Ludovic; Razmjooei, Mohammad J.; Boussaha, Myriam; Richard, James; Sizun, Jean-Pierre; Stemmerik, Lars

2018-03-01

New clay mineralogical analyses have been performed on Campanian sediments from the Tethyan and Boreal realms along a palaeolatitudinal transect from 45° to 20°N (Danish Basin, North Sea, Paris Basin, Mons Basin, Aquitaine Basin, Umbria-Marche Basin and Tunisian Atlas). Significant terrigenous inputs are evidenced by increasing proportions of detrital clay minerals such as illite, kaolinite and chlorite at various levels in the mid- to upper Campanian, while smectitic minerals predominate and represented the background of the Late Cretaceous clay sedimentation. Our new results highlight a distinct latitudinal distribution of clay minerals, with the occurrence of kaolinite in southern sections and an almost total absence of this mineral in northern areas. This latitudinal trend points to an at least partial climatic control on clay mineral sedimentation, with a humid zone developed between 20° and 35°N. The association and co-evolution of illite, chlorite and kaolinite in most sections suggest a reworking of these minerals from basement rocks weathered by hydrolysis, which we link to the formation of relief around the Tethys due to compression associated with incipient Tethyan closure. Diachronism in the occurrence of detrital minerals between sections, with detrital input starting earlier during the Santonian in the south than in the north, highlights the northward progression of the deformation related to the anticlockwise rotation of Africa. Increasing continental weathering and erosion, evidenced by our clay mineralogical data through the Campanian, may have resulted in enhanced CO2 consumption by silicate weathering, thereby contributing to Late Cretaceous climatic cooling.

[X-ray diffraction (XRD) and near infrared spectrum (NIR) analysis of the soil overlying the Bairendaba deposit of the Inner Mongolia Grassland].

PubMed

Luo, Song-ying; Cao, Jian-jin; Wu, Zheng-quan

2014-08-01

The soil samples uniformly overlying the Bairendaba deposit of the Inner Mongolia grassland were collected, and ana- lyzed with X-ray diffraction (XRD) and near infrared spectrum (NIR), for exploring the origins of the soil from the, grassland mining area and the relationship with the underground rock. The results show that the samp]s consist of quartz, graphite, carbonate, hornblende, mica, chlorite, montmorillonite, illite, berlinite, diaspore, azurite, hen tite, etc. These indicate that the soil samples were not only from the weathering products of the surface rock, but also from the underground rock mass and the alteration of the wall rock. The azurite and the hematite contained in the soil, mainly coming from the oxidation zone of the orebodies, can be used as the prospecting marks. The alteration mineral assemblage is mainly chlorite-illite-montmorillonite and it experienced the alteration process of potassic alteration-->silicification-->carbonatization-->silk greisenization-->clayization. Also, the wall rock alteration and the physical weathering processes can be accurately restored by analyzing the combination of the alteration minerals, which can provide important reference information for the deep ore prospecting and the ore deposit genesis study, improving the rate of the prospecting. The XRD and NIR with the characteristics of the economy and quickness can be used for the identification of mineral composition of soil, and in the study of mineral and mineral deposits. Especially, NIR has its unique superiority, that is, its sample request is low, and it can analyze a batch of samples quickly. With the development of INR, it will be more and more widely applied in geological field, and can play an important role in the ore exploration.

Reassessing the biogenicity of Earth’s oldest trace fossil with implications for biosignatures in the search for early life

PubMed Central

Grosch, Eugene G.; McLoughlin, Nicola

2014-01-01

Microtextures in metavolcanic pillow lavas from the Barberton greenstone belt of South Africa have been argued to represent Earth’s oldest trace fossil, preserving evidence for microbial life in the Paleoarchean subseafloor. In this study we present new in situ U–Pb age, metamorphic, and morphological data on these titanite microtextures from fresh drill cores intercepting the type locality. A filamentous microtexture representing a candidate biosignature yields a U–Pb titanite age of 2.819 ± 0.2 Ga. In the same drill core hornfelsic-textured titanite discovered adjacent to a local mafic sill records an indistinguishable U–Pb age of 2.913 ± 0.31 Ga, overlapping with the estimated age of intrusion. Quantitative microscale compositional mapping, combined with chlorite thermodynamic modeling, reveals that the titanite filaments are best developed in relatively low-temperature microdomains of the chlorite matrix. We find that the microtextures exhibit a morphological continuum that bears no similarity to candidate biotextures found in the modern oceanic crust. These new findings indicate that the titanite formed during late Archean ca. 2.9 Ga thermal contact metamorphism and not in an early ca. 3.45 Ga subseafloor environment. We therefore question the syngenicity and biogenicity of these purported trace fossils. It is argued herein that the titanite microtextures are more likely abiotic porphyroblasts of thermal contact metamorphic origin that record late-stage retrograde cooling in the pillow lava country rock. A full characterization of low-temperature metamorphic events and alternative biosignatures in greenstone belt pillow lavas is thus required before candidate traces of life can be confirmed in Archean subseafloor environments. PMID:24912193

Reassessing the biogenicity of Earth's oldest trace fossil with implications for biosignatures in the search for early life.

PubMed

Grosch, Eugene G; McLoughlin, Nicola

2014-06-10

Microtextures in metavolcanic pillow lavas from the Barberton greenstone belt of South Africa have been argued to represent Earth's oldest trace fossil, preserving evidence for microbial life in the Paleoarchean subseafloor. In this study we present new in situ U-Pb age, metamorphic, and morphological data on these titanite microtextures from fresh drill cores intercepting the type locality. A filamentous microtexture representing a candidate biosignature yields a U-Pb titanite age of 2.819 ± 0.2 Ga. In the same drill core hornfelsic-textured titanite discovered adjacent to a local mafic sill records an indistinguishable U-Pb age of 2.913 ± 0.31 Ga, overlapping with the estimated age of intrusion. Quantitative microscale compositional mapping, combined with chlorite thermodynamic modeling, reveals that the titanite filaments are best developed in relatively low-temperature microdomains of the chlorite matrix. We find that the microtextures exhibit a morphological continuum that bears no similarity to candidate biotextures found in the modern oceanic crust. These new findings indicate that the titanite formed during late Archean ca. 2.9 Ga thermal contact metamorphism and not in an early ca. 3.45 Ga subseafloor environment. We therefore question the syngenicity and biogenicity of these purported trace fossils. It is argued herein that the titanite microtextures are more likely abiotic porphyroblasts of thermal contact metamorphic origin that record late-stage retrograde cooling in the pillow lava country rock. A full characterization of low-temperature metamorphic events and alternative biosignatures in greenstone belt pillow lavas is thus required before candidate traces of life can be confirmed in Archean subseafloor environments.

Hydrated silicate minerals on Mars observed by the Mars Reconnaissance Orbiter CRISM instrument

USGS Publications Warehouse

Mustard, J.F.; Murchie, S.L.; Pelkey, S.M.; Ehlmann, B.L.; Milliken, R.E.; Grant, J. A.; Bibring, J.-P.; Poulet, F.; Bishop, J.; Dobrea, E.N.; Roach, L.; Seelos, F.; Arvidson, R. E.; Wiseman, S.; Green, R.; Hash, C.; Humm, D.; Malaret, E.; McGovern, J.A.; Seelos, K.; Clancy, T.; Clark, R.; des Marais, D.; Izenberg, N.; Knudson, A.; Langevin, Y.; Martin, T.; McGuire, P.; Morris, Robert; Robinson, M.; Roush, T.; Smith, M.; Swayze, G.; Taylor, H.; Titus, T.; Wolff, M.

2008-01-01

Phyllosilicates, a class of hydrous mineral first definitively identified on Mars by the OMEGA (Observatoire pour la Mineralogie, L’Eau, les Glaces et l’Activitié) instrument1,2, preserve a record of the interaction of water with rocks on Mars. Global mapping showed that phyllosilicates are widespread but are apparently restricted to ancient terrains and a relatively narrow range of mineralogy (Fe/Mg and Al smectite clays). This was interpreted to indicate that phyllosilicate formation occurred during the Noachian (the earliest geological era of Mars), and that the conditions necessary for phyllosilicate formation (moderate to high pH and high water activity3) were specific to surface environments during the earliest era of Mars’s history4. Here we report results from the Compact Reconnaissance Imaging Spectrometer for Mars (CRISM)4 of phyllosilicate-rich regions. We expand the diversity of phyllosilicate mineralogy with the identification of kaolinite, chlorite and illite or muscovite, and a new class of hydrated silicate (hydrated silica). We observe diverse Fe/Mg-OH phyllosilicates and find that smectites such as nontronite and saponite are the most common, but chlorites are also present in some locations. Stratigraphic relationships in the Nili Fossae region show olivine-rich materials overlying phyllosilicate-bearing units, indicating the cessation of aqueous alteration before emplacement of the olivine-bearing unit. Hundreds of detections of Fe/Mg phyllosilicate in rims, ejecta and central peaks of craters in the southern highland Noachian cratered terrain indicate excavation of altered crust from depth. We also find phyllosilicate in sedimentary deposits clearly laid by water. These results point to a rich diversity of Noachian environments conducive to habitability.

Intermediate-Depth Subduction Earthquakes Recorded by Pseudotachylyte in Dry Eclogite-Facies Oceanic Lithosphere from the Alps

NASA Astrophysics Data System (ADS)

Scambelluri, M.; Pennacchioni, G.; Gilio, M.; Bestmann, M.

2016-12-01

While geophysical studies and laboratory experiments provide much information on subduction earthquakes, field studies identifying the rock types for earthquake development and the deep seismogenic environments are still scarce. To date, fluid overpressure and volume decrease during hydrous mineral breakdown the widely favoured trigger of subduction earthquakes in serpentinized lithospheric mantle and hydrated low-velocity layers atop slabs. Here we document up to 40 cm-thick pseudotachylyte (PST) in Alpine oceanic gabbro and peridotite (2-2.5 GPa-550-620°C), the analogue of a modern cold subducting oceanic lithosphere. These rocks mostly remained unaltered dry systems; only very minor domains (<1%) record partial hydration and static eclogitic metamorphism. Meta-peridotite shows high-pressure olivine + antigorite (garnet + zoisite + chlorite after mantle plagioclase); meta-gabbro develops omphacite + zoisite + talc + chloritoid + garnet. Abundant syn-eclogitic pseudotachylyte cut the dry gabbro-peridotite and the eclogitized domains. In meta-peridotite, PST shows olivine, orthopyroxene, spinel microliths and clasts of high-pressure olivine + antigorite and garnet + zoisite + chlorite aggregates. In metagabbro, microfaults in damage zones near PST cut brecciated igneous pyroxene cemented by omphacite. In unaltered gabbro, glassy PST contains micron-scale garnet replacing plagioclase microliths during, or soon after, PST cooling. In the host rock, garnet coronas between igneous olivine and plagioclase only occur near PST and between closely spaced PST veins. Absence of garnet away from PST indicates that garnet growth was triggered by mineral seeds and by heat released by PST. The above evidence shows that pseudotachylyte formed at eclogite-facies conditions. In such setting, strong, dry, metastable gabbro-peridotite concentrate stress to generate large intermediate depth subduction earthquakes without much involvement of free fluid.

Magnetic fabric and flow direction in the Ediacaran Imider dyke swarms (Eastern Anti-Atlas, Morocco), inferred from the Anisotropy of Magnetic Susceptibility (AMS)

NASA Astrophysics Data System (ADS)

Otmane, Khadija; Errami, Ezzoura; Olivier, Philippe; Berger, Julien; Triantafyllou, Antoine; Ennih, Nasser

2018-03-01

Located in the Imiter Inlier (Eastern Saghro, Anti-Atlas, Morocco), Ediacaran volcanic dykes have been studied for their petrofabric using Anisotropy of Magnetic Susceptibility (AMS) technique. Four dykes, namely TF, TD, FF and FE show andesitic compositions and are considered to belong to the same dyke swarm. They are oriented respectively N25E, N40E, N50E, and N10E and have been emplaced during a first tectonic event. The dyke FW, oriented N90E displays a composition of alkali basalt and its emplacement is attributed to a subsequent tectonic event. These rocks are propylitized under greenschist facies conditions forming a secondary paragenesis constituted by calcite, chlorite, epidote and sericite. The dykes TF, TD, FF and FE are sub-volcanic calc-alkaline, typical of post-collisional basalts/andesites, belonging to plate margin andesites. The FW dyke shows a within-plate basalt signature; alkaline affinity reflecting a different petrogenetic process. The thermomagnetic analyses show a dominantly ferromagnetic behaviour in the TF dyke core carried by single domain Ti-poor magnetite, maghemite and pyrrhotite. The dominantly paramagnetic susceptibilities in TF dyke rims and TD, FE, FF and FW dykes are controlled by ilmenite, amphibole, pyroxene and chlorite. The magnetic fabrics of the Imider dykes, determined by our AMS study, allows us to reconstitute the tectonic conditions which prevailed during the emplacement of these two generations of volcanic dykes. The first tectonic event was characterized by a roughly NE-SW compression and the second tectonic event is characterized by an E-W shortening followed by a relaxation recording the end of the Pan-African orogeny in the eastern Anti-Atlas.

Hydrothermal alteration in oceanic ridge volcanics: A detailed study at the Galapagos Fossil Hydrothermal Field

USGS Publications Warehouse

Ridley, W.I.; Perfit, M.R.; Josnasson, I.R.; Smith, M.F.

1994-01-01

The Galapagos Fossil Hydrothermal Field is composed of altered oceanic crust and extinct hydrothermal vents within the eastern Galapagos Rift between 85??49???W and 85??55???W. The discharge zone of the hydrothermal system is revealed along scarps, thus providing an opportunity to examine the uppermost mineralized, and highly altered interior parts of the crust. Altered rocks collected in situ by the submersible ALVIN show complex concentric alteration zones. Microsamples of individual zones have been analysed for major/minor, trace elements, and strontium isotopes in order to describe the complex compositional details of the hydrothermal alteration. Interlayered chlorite-smectite and chlorite with disequilibrium compositions dominate the secondary mineralogy as replacement phases of primary glass and acicular pyroxene. Phenocrysts and matrix grains of plagioclase are unaffected during alteration. Using a modification of the Gresens' equation we demonstrate that the trivalent rare earth elements (REEs) are relatively immobile, and calculate degrees of enrichment and depletion in other elements. Strontium isotopic ratios increase as Sr concentrations decrease from least-altered cores to most-altered rims and cross-cutting veins in individual samples, and can be modeled by open system behaviour under low fluid-rock ratio (< 10) conditions following a period of lower-temperature weathering of volcanics within the rift zone. The complex patterns of element enrichment and depletion and strontium isotope variations indicate mixing between pristine seawater and ascending hot fluids to produce a compositional spectrum of fluids. The precipitation of base-metal sulfides beneath the seafloor is probably a result of fluid mixing and cooling. If, as suggested here, the discharge zone alteration occurred under relatively low fluid-rock ratios, then this shallow region must play an important role in determining the exit composition of vent fluids in marine hydrothermal systems. ?? 1994.

Tracing mineral weathering reactions in the critical zone using Mg, Ca, and Sr isotopes, Luquillo Mountains, Puerto Rico

NASA Astrophysics Data System (ADS)

Buss, H. L.; White, A. F.; Vivit, D.; Bullen, T. D.; Blum, A. E.; Dessert, C.; Gaillardet, J.

2008-12-01

Mineral weathering in the critical zone directly impacts the availability of many important soil nutrients. As part of the USGS Water Energy and Biogeochemical Budgets (WEBB) program and the Critical Zone Exploration Network, we are investigating mineral nutrient distributions and fluxes in depth profiles (to 16 m) at five sites in the Bisley 1 catchment in the Luquillo Mountains of Puerto Rico. The Bisley 1 catchment contains a thick regolith developed on marine bedded, andesitic, volcaniclastic bedrock. Pore waters were sampled as a function of depth from nested suction water samplers. Pore water chemistry was analyzed and compared to total chemistry of solid samples taken from augered cores. Mg, Ca and Sr isotope ratios were measured of the pore waters at the Institut de Physique du Globe de Paris (Mg) and at the USGS in Menlo Park, CA (Ca, Sr). The Mg isotope ratios increase with increasing depth from δ26Mg = -0.772 at the surface to - 0.267 at depth, relative to the DSM3 standard. Sr isotope ratios vary from 0.70922 to 0.71016 87Sr/86Sr, with no discernible depth trend. The regolith is highly weathered and is depleted in primary minerals (except quartz) with respect to bedrock. Volumetric strain, calculated with respect to quartz, indicates approximately 25% volume collapse occurred relative to the original volume of the bedrock. Plagioclase, chlorite, pyroxene, and amphibole weather at the bedrock-regolith interface. The regolith contains quartz, kaolinite, other clays, and iron and manganese oxides. Increasing solid and pore water Mg concentrations and δ26Mg with depth likely indicate a two step weathering process wherein high-Mg chlorite dissolves at the bedrock-regolith interface and forms Mg-containing secondary clays and oxides, which then dissolve within the regolith profile.

Pseudotachylyte in the Tananao Metamorphic Complex, Taiwan: Occurrence and dynamic phase changes of fossil earthquakes

NASA Astrophysics Data System (ADS)

Chu, Hao-Tsu; Hwang, Shyh-Lung; Shen, Pouyan; Yui, Tzen-Fu

2012-12-01

Pseudotachylyte veins and cataclasites were studied in the mylonitized granitic gneiss of the Tananao Metamorphic Complex at Hoping, Eastern Taiwan. The aphanitic pseudotachylyte veins vary in thickness, ranging from millimeters to about 1 cm. Field and optical microscopic observations show that such pseudotachylyte veins cut across cataclasites, which, in turn, transect the mylonitized granitic gneiss. Scanning electron microscopic images also show that both the pseudotachylyte veins and the cataclasites have been metasomatized by a K-rich fluid, resulting in the replacement of Na-plagioclase by K-feldspar (veins). Analytical electron microscopic observations reveal further details of physical and chemical changes (mainly fragmentation, dislocations, cleaving-healing with inclusions and relic voids, and retention of high-temperature albite) of quartz and feldspar in crushed grains. Pseudotachylytes occur as dark veins having a higher content of chlorite-biotite, clinozoisite-epidote and titanite fragments than cataclasites. These veins, coupled with hematite/jarosite-Fe-rich amorphous shell/carbonaceous material, indicate that crushing, healing/sintering, and inhomogeneous melt/fluid infiltration involving incipient and intermediate/high temperature melt patches, before and/or contemporaneous with the metasomatic K-rich fluid, prevailed in a coupled or sequential manner in the faulting event to form nonequilibrium phase assemblage. The chlorite-biotite, carbonaceous material and other nanoscale minerals could be vulnerable in future earthquakes under the influence of water. The timing of the formation of these pseudotachylyte veins should be later than the area's age of mylonitization of granitic gneiss of approximately 4.1-3.0 Ma (Wang et al., 1998). The formation of pseudotachylytes registers the fossil earthquakes during early stages in the exhumation history of the uplifting Taiwan Mountain belt since the Plio-Pleistocene Arc-Continent collision.

Provenance and accommodation pathways of late Quaternary sediments in the deep-water northern Ionian Basin, southern Italy

NASA Astrophysics Data System (ADS)

Perri, Francesco; Critelli, Salvatore; Dominici, Rocco; Muto, Francesco; Tripodi, Vincenzo; Ceramicola, Silvia

2012-12-01

The northern Calabria along the southeastern coast of Italy provides a favorable setting in which to study complete transects from continental to deep-marine environments. The present northern Ionian Calabrian Basin is a wedge-top basin within the modern foreland-basin system of southern Italy. The Ionian margin of northern Calabria consists of a moderately developed fluvial systems, the Crati and Neto rivers, and diverse smaller coastal drainages draining both the Calabria continental block (i.e., Sila Massif) and the southern Apennines thrust belt (i.e., Pollino Massif). The main-channel sand of the Crati and Neto rivers is quartzofeldspathic with abundant metamorphic and plutonic lithic fragments (granodiorite, granite, gneiss, phyllite and sedimentary lithic fragments). Sedimentary lithic fragments were derived from Jurassic sedimentary successions of the Longobucco Group. The mud samples contain mostly phyllosilicates, quartz, calcite, feldspars and dolomite. Traces of gypsum are present in some samples. The I-S mixed layers, 10 Å-minerals (illite and micas), chlorite and kaolinite are the most abundant phyllosilicates, whereas smectite and chlorite/smectite mixed layers are in small amounts. The geochemical signatures of the muds reflect a provenance characterized by both felsic and mafic rocks with a significant input from carbonate rocks. Furthermore, the degree of source-area weathering was most probably of low intensity rather than moderately intense because CIA values for the studied mud samples are low. Extrapolation of the mean erosion budget from 1 to 25 Ma suggests that at least 5 to 8 km of crust have been removed from the Calabrian orogenic belt and deposited in the marine basins. The Calabrian microplate played an important role in the dynamic evolution of southern Italian fossil and modern basins, representing the key tectonic element of the entire orogenic belt.

Clay mineralogy and its palaeoclimatic significance in the Luochuan loess-palaeosols over ˜1.3 Ma, Shaanxi, northwestern China

NASA Astrophysics Data System (ADS)

Won, Changdok; Hong, Hanlie; Cheng, Feng; Fang, Qian; Wang, Chaowen; Zhao, Lulu; Churchman, Gordon Jock

2018-03-01

To understand climate changes recorded in the Luochuan loess-palaeosols, Shaanxi province, northwestern China, clay mineralogy was studied using X-ray diffraction (XRD), high-resolution transmission electron microscopy (HRTEM), and scanning electron microscopy (SEM) methods. XRD results show that clay mineral compositions in the Luochuan loess-palaeosols are dominantly illite, with minor chlorite, kaolinite, smectite, and illite-smectite mixed-layer clays (I/S). Illite is the most abundant species in the sediments, with a content of 61%-83%. The content of chlorite ranges from 5%-22%, and the content of kaolinite ranges from 5%-19%. Smectite (or I/S) occurs discontinuously along the loess profile, with a content of 0-8%. The Kübler index of illite (IC) ranges from 0.255°-0.491°, and the illite chemical index (ICI) ranges from 0.294-0.394. The CIA values of the loesspalaeosols are 61.9-69.02, and the R3+/(R3+ + R2+ + M+) values are 0.508-0.589. HRTEM observations show that transformation of illite to illite-smectite has occurred in both the loess and palaeosol, suggesting that the Luochuan loess-palaeosols have experienced a certain degree of chemical weathering. The Luochuan loess-palaeosols have the same clay mineral assemblage along the profile. However, the relative contents of clay mineral species, CIA, ICI, and IC values fluctuate frequently along the profile, and all these parameters display a similar trend. Moreover, climate changes suggested by the clay index are consistent with variations in the deep-sea δ18O records and the magnetic susceptibility value, and thus, climate changes in the Luochuan region have been controlled by global climate change.

Distribution and possible immobilization of lead in a forest soil (Luvisol) profile.

PubMed

Sipos, Péter; Németh, Tibor; Mohai, Ilona

2005-02-01

Geochemical analyses using a sequential extraction method and lead adsorption studies were carried out in order to characterize the distribution and adsorption of lead on each genetic horizon of a Luvisol profile developed on a pelagic clayey aleurolite. Clay illuviation is the most important pedogenic process in the profile studied. Its clay mineralogy is characterized by chlorite/vermiculite species with increasing chlorite component downward. The amount of carbonate minerals strongly increases in the lower part of the profile resulting in an abrupt rise in soil pH within a small distance. The Pb content of the soil profile exceeds the natural geochemical background only in the Ao horizon, and its amount decreases with depth in the profile without correcting for differences in bulk density, suggesting the binding of Pb to soil organic matter. According to the sequential extraction analysis the organic matter and carbonate content of the soil have the most significant effect on lead distribution. This effect varies in the different soil horizons. Lead adsorption experiments were carried out on whole soil samples, soil clay fractions, as well as on their carbonate and organic matter free variant. The different soil horizons adsorb lead to different extents depending on their organic matter, clay mineral and carbonate content; and the mineralogical features of soil clays significantly affect their lead adsorption capacity. The clay fraction adsorbs 25% more lead than the whole soil, while in the calcareous subsoil a significant proportion of lead is precipitated due to the alkaline conditions. 10 and 5% of adsorbed Pb can be leached with distilled water in the organic matter and clay mineral dominated soil horizons, respectively. These results suggest that soil organic matter plays a decisive role in the adsorption of Pb, but the fixation by clay minerals is stronger.

Evaluation of mineral-aqueous chemical equilibria of felsic reservoirs with low-medium temperature: A comparative study in Yangbajing geothermal field and Guangdong geothermal fields

NASA Astrophysics Data System (ADS)

Li, Jiexiang; Sagoe, Gideon; Yang, Guang; Lu, Guoping

2018-02-01

Classical geothermometers are useful tools for estimating reservoir temperatures of geothermal systems. However, their application to low-medium temperature reservoirs is limited because large variations of temperatures calculated by different classical geothermometers are usually observed. In order to help choose the most appropriate classical geothermometer for calculating the temperatures of low-medium temperature reservoirs, this study evaluated the mineral-aqueous equilibria of typical low-medium temperature felsic reservoirs in the Yangbajing geothermal field and Guangdong geothermal fields. The findings of this study support that reservoirs in the Guangdong geothermal fields have no direct magma influence. Also, natural reservoirs may represent the intermediate steady state before reaching full equilibrium, which rarely occurs. For the low-medium temperature geothermal systems without the influence of magma, even with seawater intrusion, the process of minerals reaching mineral-aqueous equilibrium is sequential: chlorite and chalcedony are the first, then followed by K-feldspar, kaolinite and K-mica. Chlorite may reach equilibrium at varying activity values, and the equilibrium between K-feldspar and kaolinite or K-feldspar and K-mica can fix the contents of K and Al in the solutions. Although the SiO2 and Al attain equilibrium state, albite and laumontite remain unsaturated and thus may affect low-medium temperature calculations. In this study, the chalcedony geothermometer was found to be the most suitable geothermometer for low-medium temperature reservoirs. The results of K-Mg geothermometer may be useful to complement that of the chalcedony geothermometer in low-medium temperature reservoir systems. Na-K geothermometer will give unreliable results at low-medium temperatures; and Na-K-Ca will also be unsuitable to calculate reservoir temperatures lower than 180 °C, probably caused by the chemical imbalance of laumontite.

Environmental effect and genetic influence: a regional cancer predisposition survey in the Zonguldak region of Northwest Turkey

NASA Astrophysics Data System (ADS)

Kadir, Selahattin; Önen-Hall, A. Piril; Aydin, S. Nihal; Yakicier, Cengiz; Akarsu, Nurten; Tuncer, Murat

2008-03-01

The Cretaceous-Eocene volcano-sedimentary units of the Zonguldak region of the western Black Sea consist of subalkaline andesite and tuff, and sandstone dominated by smectite, kaolinite, accessory chlorite, illite, mordenite, and analcime associated with feldspar, quartz, opal-CT, amphibole, and calcite. Kaolinization, chloritization, sericitization, albitization, Fe-Ti-oxidation, and the presence of zeolite, epidote, and illite in andesitic rocks and tuffaceous materials developed as a result of the degradation of a glass shards matrix, enclosed feldspar, and clinopyroxene-type phenocrysts, due to alteration processes. The association of feldspar and glass with smectite and kaolinite, and the suborientation of feldspar-edged, subparallel kaolinite plates to fracture axes may exhibit an authigenic smectite or kaolinite. Increased alteration degree upward in which Al, Fe, and Ti are gained, and Si, Na, K, and Ca are depleted, is due to the alteration following possible diagenesis and hydrothermal activities. Micromorphologically, fibrous mordenite in the altered units and the presence of needle-type chrysotile in the residential buildings in which cancer cases lived were detected. In addition, the segregation pattern of cancer susceptibility in the region strongly suggested an environmental effect and a genetic influence on the increased cancer incidence in the region. The most likely diagnosis was Li-Fraumeni syndrome, which is one of the hereditary cancer predisposition syndromes; however, no mutations were observed in the p53 gene, which is the major cause of Li-Fraumeni syndrome. The micromorphology observed in the altered units in which cancer cases were detected may have a role in the expression of an unidentified gene, but does not explain alone the occurrence of cancer as a primary cause in the region.

Mineralogy, morphology, and textural relationships in coatings on quartz grains in sediments in a quartz-sand aquifer

USGS Publications Warehouse

Zhang, Shouliang; Kent, Douglas B.; Elbert, David C.; Shi, Zhi; Davis, James A.; Veblen, David R.

2011-01-01

Mineralogical studies of coatings on quartz grains and bulk sediments from an aquifer on Western Cape Cod, Massachusetts, USA were carried out using a variety of transmission electron microscopy (TEM) techniques. Previous studies demonstrated that coatings on quartz grains control the adsorption properties of these sediments. Samples for TEM characterization were made by a gentle mechanical grinding method and focused ion beam (FIB) milling. The former method can make abundant electron-transparent coating assemblages for comprehensive and quantitative X-ray analysis and the latter technique protects the coating texture from being destroyed. Characterization of the samples from both a pristine area and an area heavily impacted by wastewater discharge shows similar coating textures and chemical compositions. Major constituents of the coating include Al-substituted goethite and illite/chlorite clays. Goethite is aggregated into well-crystallized domains through oriented attachment resulting in increased porosity. Illite/chlorite clays with various chemical compositions were observed to be mixed with goethite aggregates and aligned sub-parallel to the associated quartz surface. The uniform spatial distribution of wastewater-derived phosphorus throughout the coating from the wastewater-contaminated site suggests that all of the coating constituents, including those adjacent to the quartz surface, are accessible to groundwater solutes. Both TEM characterization and chemical extraction results indicate there is a significantly greater amount of amorphous iron oxide in samples from wastewater discharge area compared to those from the pristine region, which might reflect the impact of redox cycling of iron under the wastewater-discharge area. Coating compositions are consistent with the moderate metal and oxy-metalloid adsorption capacities, low but significant cation exchange capacities, and control of iron(III) solubility by goethite observed in reactive transport experimental and modeling studies conducted at the site.

Alteration mineralogy, mineral chemistry and stable isotope geochemistry of the Eocene pillow lavas from the Trabzon area, NE Turkey

NASA Astrophysics Data System (ADS)

Abdioğlu Yazar, Emel

2018-02-01

The Eocene subaqueous volcanic units in NE Turkey developed as pillow, closely packed pillow, isolated pillow, pillow breccia, hyaloclastite breccia and rare peperitic facies with red micritic limestones. They are locally set on volcaniclastic sandstone and claystone alternations and gradually pass to tuffs and volcanic breccias. The pillow lava samples generally exhibit intersertal, intergranular, microlitic porphyritic, variolitic, vesicular and glomeroporphyritic and glassy textures with clinopyroxene (Wo47-52En40-45Fs6-8), plagioclase (An10 to An96), olivine (Fo79-87) and Fe-Ti oxides (Usp0-0.27). Saponite, interlayered chlorite/saponite, rare beidellite and calcite were determined after olivine, rarely after plagioclase as well as in the glassy groundmass. Illite was restricted to plagioclase and the glassy groundmass. Na-Ca zeolites, chlorites/saponites, beidellite, dolomite and calcite occur as void infillings and in the glassy groundmass. Mineralogical, lithochemical and isotopic interpretations as well as thermometric calculations reveal a low-temperature seawater alteration in a semi-closed environment for the alteration of primary minerals and volcanic glass in addition to sealed vesicles and open systems for crosscutting veins. Due to the short exposure time intervals of seawater to rocks, the total chemistry of the rocks is not fully changed and most of the elements seem to be immobile, remaining in the system as a result of precipitation in voids and cracks. Thermometric estimations indicate that, the temperature of heated seawater is approximately 160 °C at the highest point especially in the vesicles, and decreases to approximately 85 °C due to circulation, resulting in alterations of the primary phases and volcanic glass.

The CR (Renazzo-type) carbonaceous chondrite group and its implications

NASA Technical Reports Server (NTRS)

Weisberg, Michael K.; Prinz, Martin; Clayton, Robert N.; Mayeda, Toshiko K.

1993-01-01

A petrologic, geochemical, and oxygen isotropic study of the CR chondrites including Renazzo, Al Rais, El Djouf 001 and the paired Acfer meteorites, EET87770 and the paired samples, MAC87320, Y790112, Y793495, and Y791498 is presented. It is concluded that the CR group is characterized by abundant large multilayered, Fe, Ni metal-rich, type I chondrules; abundant matrix and dark inclusions; unique assemblages of serpentine and chlorite-rich phyllosilicates and Ca-carbonates; Ca-carbonate rims on chondrules; abundant Fe, Ni metal with a positive Ni vs. Co trend and a solar Ni:Co ratio; and amoeboid olivine aggregates with Mn-rich and Mn-poor forsterite.

HYDROTHERMAL MINERALOGY OF RESEARCH DRILL HOLE Y-3, YELLOWSTONE NATIONAL PARK, WYOMING.

USGS Publications Warehouse

Bargar, Keith E.; Beeson, Melvin H.

1984-01-01

The approximate paragenetic sequence of hydrothermal minerals in the Y-3 U. S. Geological Survey research diamond-drill hole in Lower Geyser Basin, Yellowstone National Park, Wyoming, is: hydrothermal chalcedony, hematite, pyrite, quartz, clay minerals (smectite and mixed-layer illite-smectite), calcite, chlorite, fluorite, pyrite, quartz, zeolite minerals (analcime, dachiardite, laumontite, stilbite, and yugawaralite), and clay minerals (smectite and mixed-layer illite-smectite). A few hydrothermal minerals that were identified in drill core Y-3 (lepidolite, aegirine, pectolite, and truscottite) are rarely found in modern geothermal areas. The alteration minerals occur primarily as vug and fracture fillings that were deposited from cooling thermal water. Refs.

Stratigraphic setting and mineralogy of the Arctic volcanogenic massive sulfide prospect, Ambler district, Alaska.

USGS Publications Warehouse

Schmidt, J.M.

1986-01-01

The Arctic prospect, south central Brooks Range, is among the 30 largest of 508 volcanic-hosted massive sulphide deposits in the world. The massive sulphide lenses are interlayered with graphitic schist between metamorphosed rhyolite porphyries in Middle Devonian to early Mississippian metamorphosed volcanic, volcaniclastic and sedimentary rocks. Hydrothermal alteration is of three types: chloritic, phyllic s.l., and pyrite-phengite, each type strata-distinctively and respectively below, in, and above the sulphides. Maximum alteration conforms with metal zoning in the sulfides to suggest predominantly northwestward dispersal from a linear vent area in the elongate basin containing the deposit.-G.J.N.

Geology and ore deposits of the Mahd Adh Dhahab District, Kingdom of Saudi Arabia

USGS Publications Warehouse

Luce, Robert W.; Bagdady, Abdulaziz; Roberts, Ralph Jackson

1976-01-01

The principal ore minerals are pyrite, chalcopyrite, sphalerite, galena, and minor tetrahedrite, argentite, and native gold and silver. The gold and silver occurs finely disseminated in the veins and in the altered selvages of the veins. Widespread potassic and propylitic alteration accompanied the ore-forming processes. Potassium feldspar was introduced during an early stage of vein formation. Isotopic analyses of lead in vein potassium feldspar and galena yield a model age of about 900-1050 million years with the possibility of the original lead source having been remobilized about 600 million years ago. Chlorite and carbonate are also prominent vein minerals.

Mineralogy and diagenesis of low-permeability sandstones of Late Cretaceous age, Piceance Creek Basin, northwestern Colorado

USGS Publications Warehouse

Hansley, Paula L.; Johnson, Ronald C.

1980-01-01

This report presents preliminary results of a mineralogic and diagenetic study of some low-permeability sandstones from measured surface sections and cores obtained from drill holes in the Piceance Creek Basin of northwestern Colorado. A documentation of the mineralogy and diagenetic history will aid in the exploration for natural gas and in the development of recovery technology in these low-permability sandstones. These sandstones are in the nonmarine upper part of the Mesaverde Formation (or Group) of Late Cretaceous age and are separated from overlying lower Tertiary rocks by a major regional unconformity. Attention is focused on the sandstone units of the Ohio Creek Member, which directly underlies the unconformity; however, comparisons between the mineralogy of the Ohio Creek strata and that of the underlying sandstone units are made whenever possible. The Ohio Creek is a member of the Hunter Canyon Formation (Mesaverde Group) in the southwestern part of the basin, and the Mesaverde Formation in the southern and central parts of the basin. The detrital mineralogy is fairly constant throughout all of these nonrnarine Cretaceous sandstone units; however, in the southeastern part of the basin, there is an increase in percentage of feldspar, quartzite, and igneous rock fragments in sandstones of the Ohio Creek Member directly underlying the unconformity. In the southwestern part of the basin, sandstones of the Ohio Creek Member are very weathered and are almost-entirely comprised of quartz, chert, and kaolinite. A complex diagenetic history, partly related to the overlying unconformity, appears to be responsible for transforming these sandstones into potential gas reservoirs. The general diagenetic sequence for the entire Upper Cretaceous interval studied is interpreted to be (early to late): early(?) calcite cement, chlorite, quartz overgrowths, calcite cement, secondary porosity, analcime (surface only), kaolinite and illite, and late carbonate cements. Authigenic high-iron chlorite, which occurs on grain rims and in pore throats, is primarily responsible for the low-permeability of the subsurface sandstones of the Ohio Creek Member in the center of the basin. Kaolinite is the most abundant pore-filling authigenic clay in these sandstones, from the southwestern part of the basin and is responsible for their distinctive white-weathering color in outcrop. In the sandstones below the Ohio Creek Member, however, chlorite and kaolinite occur locally, and authigenic calcite and illite are more abundant. The occurrence and distribution of secondary porosity is one of the most important aspects of the diagenetic history of these sandstones. It is present as moldic intra- and intergranular porosity, as well as microporosity among authigenic clay pariicles. Although present locally in most sandstone units, secondary porosity is particularly common in the uppermost sandstone units and is interpreted to have formed primarily asa result ofweathering during the time represented by the Cretaceous-Tertiary unconformity.

The Freyenstein Shear Zone - Implications for exhumation of the South Bohemian Batholith (Moldanubian Superunit, Strudengau, Austria)

NASA Astrophysics Data System (ADS)

Griesmeier, Gerit; Iglseder, Christoph; Konstantin, Petrakakis

2016-04-01

The Moldanubian superunit is part of the internal zone of the Variscan Orogen in Europe and borders on the Saxothuringian and Sudetes zones in the north. In the south, it is blanketed by the Alpine foreland molasse. Tectonically it is subdivided into the Moldanubian Nappes (MN), the South Bohemian Batholith (SBB) and the Bavarian Nappes. This work describes the ~ 500 m thick Freyenstein shear zone, which is located at the southern border of the Bohemian Massif north and south of the Danube near Freyenstein (Strudengau, Lower Austria). The area is built up by granites of Weinsberg-type, which are interlayered by numerous dikes and paragneisses of the Ostrong nappe system. These dikes include medium grained granites and finegrained granites (Mauthausen-type granites), which form huge intrusions. In addition, smaller intrusions of dark, finegrained diorites und aplitic dikes are observed. These rocks are affected by the Freyenstein shear zone und ductily deformed. Highly deformed pegmatoides containing white mica crystals up to one cm cut through the deformed rocks and form the last dike generation. The Freyenstein shear zone is a NE-SW striking shear zone at the eastern edge of the SBB. The mylonitic foliation is dipping to the SE with angles around 60°. Shear-sense criteria like clast geometries, SĆ structures as well as microstructures show normal faulting top to S/SW with steep (ca. 50°) angles. The Freyenstein shear zone records a polyphase history of deformation and crystallization: In a first phase, mylonitized mineral assemblages in deformed granitoides can be observed, which consist of pre- to syntectonic muscovite-porphyroclasts and biotite as well as dynamically recrystallized potassium feldspar, plagioclase and quartz. The muscovite porphyroclasts often form mica fishes and show top to S/SW directed shear-sense. The lack of syntectonic chlorite crystals points to metamorphic conditions of lower amphibolite-facies > than 450° C. In a later stage fluid infiltration under lower greenschist-facies conditions locally lead to sericitization of feldspar and development of pseudomorphs after it. In addition, syn-mylonitic biotite has been chloritized mimetically. Chlorite growth across the mylonitic foliation occurs rarely. Brittle faulting, overprinting the shear zone features, is documented by the occurrence of numerous harnish planes. They show normal faulting to the N with angles around 30° and locally sinistral shear-sense. The Freyenstein shear zone belongs to a system of NE-SW striking shear zones and faults in the Moldanubian superunit and is located at the border between the SBB and MN ductily deforming both. Therefore, it plays an important role in exhumation processes of last stage SBB (synkinematic) intrusions during Late Variscan orogenic extension. According to cooling ages in other shear zones and (synkinematic) intrusions an age of ca. 320-290 Ma for the ductile deformation can be assumed.

The dynamics of serpentinite dehydration reactions in subduction zones: Constrains from the Cerro del Almirez ultramafic massif (Betic Cordillera, SE Spain)

NASA Astrophysics Data System (ADS)

Dilissen, Nicole; Garrido, Carlos J.; López Sánchez-Vizcaíno, Vicente; Padrón-Navarta, José Alberto

2015-04-01

Arc volcanism, earthquakes and subduction dynamics are controlled by fluids from downgoing slabs and their effect on the melting and rheology of the overlying mantle wedge. High pressure dehydration of serpentinite in the slab and the subduction channel is considered as one of the main sources of fluids in subduction zones. Even though this metamorphic reaction is essential in subduction activities, the behavior of the fluids, the kinetics and thermodynamics during the breakdown reaction are still poorly understood. The Cerro del Almirez (Nevado-Filábride Complex, Betic Cordillera, SE Spain) uniquely preserves the dehydration front from antigorite serpentinite to chlorite-harzburgite and constitutes a unique natural laboratory to investigate high-pressure dehydration of serpentinite. This reaction occurred in a subduction setting releasing up to 13 wt% of water, contributing significantly to the supply of fluids to the overlying mantle wedge. A key to the understanding of the metamorphic conditions prevailing during serpentinite dehydration is to study the two prominent textures -granofels and spinifex-like chlorite harzburgite- occurring in this reaction product. The detailed texture differences in the Chl-harzburgite can provide insights into diverse kinetic and thermodynamic conditions of this dehydration reaction due to variations in effective pressure and drainage conditions. It has been proposed that difference in overpressure (P') and deviation from growth equilibrium, i.e. overstepping, is responsible for these two types of textures [Padrón-Navarta et al., 2011]. The magnitude and duration of P' is highly dependent on dehydration kinetics [Connolly, 1997]. The fast pressure drop, with spinifex-texture as a product, can be linked to draining events expected after hydrofracturing, which are recorded in grain size reduction zones in this massif. According to this hypothesis, mapping of textural variation in Chl-harzburgite might be used as a proxy to investigate the hydrodynamics of serpentinite dehydration reaction. During an intensive detailed field mapping of a well-exposed area of ca. 0.87 km2 in the W-SW part of the massif, we mapped textural variations of Chl-harzburgite every three to ten meters. Granofels and spinifex lenses occur within scales of decimetres to decametres. These spatial scale constrains can be linked to temporal scales of the reactions and to the spatial and temporal variation of fluid release during dehydration of serpentinite. REFERENCES Connolly, J. A. D. (1997), Devolatilization-generated fluid pressure and deformation-propagated fluid flow during prograde regional metamorphism, J. Geophys. Res.-Solid Earth, 102(B8), 18149-18173, doi:10.1029/97jb00731. Padrón-Navarta, J. A., V. López Sánchez-Vizcaíno, C. J. Garrido, and M. T. Gómez-Pugnaire (2011), Metamorphic record of high-pressure dehydration of antigorite serpentinite to chlorite harzburgite in a subduction setting (Cerro del Almirez, Nevado-Filábride Complex, southern Spain), Journal of Petrology, 52(10), 2047-2078.

Greenschist-Facies Pseudotachylytes and Gouge: a Microstructural Study of the Deformation Propagation at the Boundary Between Hp-Metabasite and Calcite Bearing Metasediments

NASA Astrophysics Data System (ADS)

Crispini, L.; Scambelluri, M.; Capponi, G.

2013-12-01

Recent friction experiments on calcite-bearing systems reproduce pseudotachylyte structures, that are diagnostic of dinamic calcite recrystallization related to seismic slip in the shallow crust. Here we provide the study of a pseudotachylyte (PT) bearing low angle oblique-slip fault. The fault is linked to the exhumation of Alpine HP-ophiolites and it is syn- to post-metamorphic with respect to retrograde greenschist facies metamorphism. The observed microstructures developed at the brittle-ductile transition and suggest that seismic and interseismic slip was enhanced by interaction with fluids. The fault zone is in-between high-pressure eclogite-facies metabasites (hangingwall) and calcite bearing metasediments (footwall). The mafic rocks largely consist of upper greenschist facies hornblende, albite, chlorite, epidote with relict eclogitic garnet, Na-pyroxene and rutile; metasediments correspond to calcschist and micaschist with quartz, phengite, zoisite, chlorite, calcite and relics of garnet. Key features of the oucrop are: the thickness and geometry of the PT and gouge; the multiple production of PT characterized by overprinting plastic and brittle deformation; the occurrence in footwall metasediments of mm-thick bands of finely recrystallized calcite coeval with PT development in the hangingwall. The damage zone is ca. 2 m-thick and is characterized by two black, ultra-finegrained straight and sharp Principal Slip Zones (PSZ) marked by PT. The damage zone shows a variety of fault rocks (cataclasite and ultracataclasite, gouge and PT) with multiple crosscutting relationships. Within the two main PSZ, PT occurs in 10-20 cm thick layer, in small scale injection veins and in microfractures. In the mafic hanging wall, the PT is recrystallized and does not preserve glass: it shows flow structures with subrounded, embayed and rebsorbed quartz in a fine grained matrix composed of isotropic albite + chlorite + quartz + epidote + titanite, suggesting recrystallization at ca. 270-300°C, 8-10 km of the original glass. PT show plastic deformations overprinted by shear bands and fracturing. The matrix of cataclastic layers has the same mineral assemblage as PT and clasts of recrystallised PT, to indicate polyphase PSZ formation. In the metasedimentary footwall, the original foliation is deflected parallel to the PSZ and is cut by cm-spaced shear bands parallel to PSZ. Deformation propagates in the footwall through mm-thick injections veins, shear bans, P-shears and veins. Pockets of recrystallized PT occur along the pre-existing mylonitic foliation of metasediments. Worthnote is the presence of mm-thick deformation bands (CDB) that are post-mylonitic foliation and mainly composed of fine grained calcite bounded by dissolution seams or ribbon grains of deformed calcite. CDB are characterised by subrounded embayed and rebsorbed quartz grains rimmed by new Ca-Mg amphibole, K-feldspar (90-93%K), in a dinamic recrystallized calcite 2-10 micron in size and slightly elongated. The features of the CDB suggest that these structures can be considered as diagnostic of localised deformation during coesismic slip in metasedimentary rocks.

Geology and geochemistry of paleosols developed on the Hekpoort Basalt, Pretoria Group, South Africa

NASA Technical Reports Server (NTRS)

Rye, R.; Holland, H. D.

2000-01-01

The Hekpoort paleosols comprise a regional paleoweathering horizon developed on 2.224 +/- 0.021 Ga basaltic andesite lavas at the top of the Hekpoort Formation of the Pretoria Group, Transvaal Supergroup, South Africa. In five separate profiles, from outcrops along road cuts near Waterval Onder and the Daspoort Tunnel and in three drill cores from the Bank Break Area (BB3, BB8, and BB14), the top of the paleosol is a sericite-rich zone. The sericite zone grades downward into a chlorite-rich zone. In core BB8 and in the road cut at the Daspoort Tunnel, we sampled the underlying or parent basaltic andesite into which the chlorite zone grades. We did not obtain samples of the parent material at Waterval Onder and in cores BB3 and BB14, but chemical analyses indicate that the chlorite and sericite zones in these profiles derive from underlying lavas similar to the ones we sampled in core BB8 and at the Daspoort Tunnel. The presence of apparent rip-up clasts of the paleosol in the overlying ironstones of the Strubenkop Formation in the cores from Bank Break makes it very unlikely that most of the alteration was a result of interactions with hydrothermal fluids. Desiccation cracks at the top of the paleosol that were filled with sand during the deposition of the overlying sediments at Waterval Onder point to a subaerial weathering origin. Very little, if any, Al, Ti, Zr, V, or Cr moved a discernible distance during weathering of any of the five profiles. The vertical distribution of Fe, Mg, Mn, Ni, and Co indicates that these elements were largely removed from the top of the soil during weathering. The overall abundance of these elements in each of the profiles indicates that a significant fraction of the complement lost from the top subsequently reprecipitated in the lower portion of the soil as constituents of an Fe2(+) -rich smectite. The loss of Fe from the top of the soil during weathering of the Hekpoort paleosols indicates that atmospheric PO2 was less than 8 x 10(-4) atm about 2.22 Ga. Fe2(+) -rich smectite should only precipitate during soil formation if atmospheric PCO2 is less than or equal to 2 x 10(-2) atm (Rye, Kuo, and Holland, 1995). Ca and Na were largely lost during weathering. Some Na was apparently added to the sericite zone in cores BB3, BB8, and BB14 after weathering. All five profiles are enriched in K and Rb, and most are enriched in Ba. The distribution of these elements indicates that they all were added during post-weathering hydrothermal metasomatism. Rb-Sr analysis of the paleosol at the Daspoort Tunnel indicates that metasomatism last affected that profile 1.925 +/- 0.032 Ga (Macfarlane and Holland, 1991).

The Fortuna gold skarn, Nambija district, Ecuador - A mineralogical and fluid inclusion study

NASA Astrophysics Data System (ADS)

Markowski, A.; Fontboté, L.; Chiaradia, M.

2003-04-01

La Fortuna gold skarn is located in the nothern part of the Nambija gold district, southern Ecuador. As other Nambija deposits (Meinert, 2000) it is an oxidized-calcic gold skarn. The skarn has developed on volcanic rocks belonging to the Triassic Piunza Formation and nearby undated felsic intrusions. Main skarn bodies and Au concentrations occur near major N40°-60°faults. Garnet is the dominant phase at the Fortuna skarn, which displays two types according to garnet color and composition: a brown massive garnet (Ad99-37) skarn and a green garnet (Ad55-13) skarn. Garnets are strongly zoned and compositions out of these ranges exist too. Additionally, the correlation between color and composition is not always clear. Some honey-reddish garnet (Ad97.0-99.5) nodules up to a few centimeters in size occur both within the brown and the green garnet skarns. Because of its position typically at the borders of open space fillings, this garnet is interpreted to reflect the composition of the fluid. Pyroxene is present as a minor phase except in the northern part of the concession and around the presently mined site ("mina 2") where pyroxene and pyroxene-garnet skarns are recognized, respectively. Compositions range from Hd42Di47Jo11 to Hd17Di63Jo20. Increases in Mn (2.5-6 wt%) and, less pronounced, in Fe (7-11 wt%) are recognized from the presently mined site to 1 km to the north. Pyroxene occurs mainly as small subidiomorphic grains, which in part appear to replace garnet (mainly the green variety). In the northern part of the mine, epidote (Epi9.8-17.7) occurs as the main phase, and is a retrograde product of garnet. The small amount of amphibole present at Fortuna is attributed to the original scarcity of pyroxene of which amphibole is the typical retrograde product. Chlorite is also an abundant phase, mainly nearby faults, and reveals variable compositions with a F/FM ranging from 0.87 to 0.38. As pyroxene, chlorite shows an enrichement in Mn (up to 4 wt.%) to the north. Other retrograde minerals are K-feldspar, plagioclase, quartz and calcite. These minerals, together with epidote and chlorite, occur mainly within cm-wide veins (N40E-N60E) and irregular open spaces. Thinner calcite veinlets do not show preferential orientation. Native gold (Ag content: 5.9 to 14.6 wt%, traces of Cu and Hg) occurs with calcite and quartz within garnet fractures or between mineral joints. Hematite seems to appear more frequently than pyrite when gold is present and could indicate a high oxygen fugacity during gold deposition. Quartz inclusions have homogenization temperatures between 350°C and 200°C, low salinities (1.2-6.0 wt% NaCl eq.), and variable liquid/vapor ratios.

Effets thermique et hydrothermal de la coulée de basalte triasico-liasique sur les argiles du bassin d'Argana (Maroc)Thermal and hydrothermal effects of Triassic Liassic basalt flow deposition on clays (Agana Basin, Morocco)

NASA Astrophysics Data System (ADS)

Daoudi, Lahcen; Pot de Vin, Jean-Luc

Thermal and hydrothermal effects of Triassic-Liassic basalt flow deposition on sedimentary series of the Argana Basin are responsible for major modifications in detrital clays, until 20 m in depth. It expressed by transformation of detrital smectite to corrensite and moreover to chlorite, and by increasing illite crystallinity. On the 2 m of sediments located immediately under the flow, magnesium-rich hydrothermal fluids have caused precipitation of new mineral phases. To cite this article: L. Daoudi, J.-L. Pot de Vin, C. R. Geoscience 334 (2002) 463-468.

Rayleigh-type parametric chemical oscillation.

PubMed

Ghosh, Shyamolina; Ray, Deb Shankar

2015-09-28

We consider a nonlinear chemical dynamical system of two phase space variables in a stable steady state. When the system is driven by a time-dependent sinusoidal forcing of a suitable scaling parameter at a frequency twice the output frequency and the strength of perturbation exceeds a threshold, the system undergoes sustained Rayleigh-type periodic oscillation, wellknown for parametric oscillation in pipe organs and distinct from the usual forced quasiperiodic oscillation of a damped nonlinear system where the system is oscillatory even in absence of any external forcing. Our theoretical analysis of the parametric chemical oscillation is corroborated by full numerical simulation of two well known models of chemical dynamics, chlorite-iodine-malonic acid and iodine-clock reactions.

Detection of hexamethonium-perchlorate association complexes using NACE-MS.

PubMed

Groom, Carl A; Hawari, Jalal

2007-02-01

Perchlorate (ClO(4) (+)) and other chlorine oxide anions were observed to complex weakly with hexamethonium (1,6-bis-(trimethylammonium)-hexane) in both aqueous and polar nonaqueous solvents. The resultant positively charged complexes were resolved by NACE using 2-propanol/acetone electrolytes prior to mass spectrometric detection using an Agilent(3D)CE system coupled to a Bruker Esquire 3000+ quadrupole IT mass detector. Using electrokinetic injection, the method detection limit for perchlorate in nonaqueous media was 10 microg/L. The isotope patterns due to the presence of (35)Cl and (37)Cl in complex mass spectra allowed for unambiguous identification of perchlorate, chlorate (ClO(3) (+)), chlorite (ClO(2) (+)), and chloride (Cl(+)) in photoreaction samples.

Geomorphological stability of Permo-Triassic albitized profiles - case study of the Montseny-Guilleries High (NE Iberia)

NASA Astrophysics Data System (ADS)

Parcerisa, D.; Casas, L.; Franke, C.; Gomez-Gras, D.; Lacasa, G.; Nunez, J. A.; Thiry, M.

2010-05-01

Massif paleoalteration profiles (≥ 200 m) occur in the upper parts of the Montseny-Guilleries High (NE Catalan Coastal Ranges). The profiles consist of hard albitized-chloritized-hematized facies in the lower part and softer kaolinized-hematized facies in the upper part of the section. Preliminary paleomagnetic data show Triassic ages for both, the albitized and the kaolinized parts, and point to a surficial formation altered under oxidising conditions. Similar paleoalteration profiles have already been described and dated to Triassic ages elsewhere in Europe [Schmitt, 1992; Ricordel et al., 2007; Parcerisa et al., 2009]. These Permian-Triassic alterations are following a succession of different mineral transformations from the top to the base of the profile: 1) Red facies are defined by an increase in the amount and size of haematite crystals leading to the red colour of the rocks. The increase on haematite content is pervasively affecting the whole rock and is accompanied by the kaolinitization of the feldspars. 2) Pink facies: here, the granite shows an uniform pink colouration, which is mainly due to the albitization of the primary Ca-bearing plagioclases, accompanied by a precipitation of minute haematite, sericite, and calcite crystals inside the albite. Additionally primary biotite is fully chloritized. The pink granites are much more resistant to the present-day weathering than the "unaltered" facies at the base of the profile. 3) Spotted facies is characterized by a partial alteration of the rock, which caused a pink-screened aspect to the rock. The alteration developed along the fractures and is less well developed or absent in the non-fractured zones. In the pink-screened facies, the plagioclases are partially albitized and contain numerous hematite inclusions. Biotites are usually almost entirely chloritized. 4) Unaltered facies: These granites are coloured white to greyish, containing plagioclase and K-feldspar that do not show any trace of albitization. Biotites are not or weakly chloritized. However, these "unaltered" (or primary) granites are strongly weathered into granite boulders embedded in grus by the present-day climatic conditions. The maturest paleoprofiles occur at the northern part of the Catalan Coastal Ranges (i.e. the Montseny-Guilleries High) where the Variscan basement remained exposed during Triassic times. Towards the South the profiles progressively disappear and Triassic sediments acquire their maximum thickness here. The alteration profiles are related with the Permo-Triassic paleosurface still outcroping on wide areas [Gómez-Gras and Ferrer, 1999]. They are partially covered by Triassic fluvial sandstones (Buntsandstein facies) in the South [Gómez-Gras, 1993] and by Palaeocene alluvial conglomerates in the West [Anadón et al., 1979]. The Triassic paleosurface shows a remarkable stability successively outcropping during Mesozoic and Tertiary times, the pre-Tertiary exhumation and even the present day weathering affected very little these albitized profiles. The hardness and thus preservation of the Triassic paleosurface is mainly related to the albitization. The albitized granites are entirely lacking anorthitic plagioclase, which is much more sensitive to chemo-mechanical weathering. Development of albite and additional chloritization of the primary biotite crystals render the rocks much more resistant to weathering and erosion. This stability is particularly well expressed in case of the Montseny-Guilleries High, which is limited by a high fault scarp at the south-eastern margin. The albitized top of the scarp shows remarkably hard fresh rocks, whereas the base of the scarp (formed of primary, non-albitized facies) is deeply weathered into gruss. This is causing much smother landscape reliefs in the valleys and thalwegs. Since a long time the remarkable persistence of the Triassic paleosurface expressed in the Paleozoic massifs has been highlighted by geomorphologists. Only recently we could draw the link of the paleosurface preservation to its albitisation [Battiau-Queney, 1996; Widdowson, 1997]. Anadón, P., Colombo, F., Esteban, M., Marzo, M., Robles, S., Santanach, P., Solé-Sugrañes, L.., 1979. Evolución tectonostratigráfica de los Catalánides. Acta Geológica Hispánica, 14: 242-270. Battiau-Queney Y., 1996, A tentative classification of paleoweathering formations based on geomorphological criteria. Geomorphology, 16, p. 87-102. Gómez-Gras, D., 1993. El Permotrias de la Cordillera Costero Catalana: facies y petrologia sedimentaria (Parte I). Boletin Geologico y Minero, 104(2): 115-161. Gómez-Gras, D., Ferrer, C., 1999. Caracterización petrológica de perfiles de meteorización antiguos desarrollados en granitos tardihercínicos de la Cordillera Costero Catalana. Revista de la Sociedad Geológica de España, 12(2): 281-299. Parcerisa, D., Thiry, M., Schmitt, J.M., 2009. Albitisation related to the Triassic unconformity in igneous rocks of the Morvan Massif (France). International Journal of Earth Sciences (Geol Rundsch). DOI 10.1007/s00531-008-0405-1 Ricordel, C., Parcerisa, D., Thiry, M., Moreau, M.G., Gómez-Gras, D., 2007. Triassic magnetic overprints related to albitization in granites from the Morvan massif (France). Palaeogeography, Palaeoclimatology, Palaeoecology, 251: 268-282. Schmitt J.M., 1992, Triassic albitization in southern France : an unusual mineralogical record from a major continental paleosurface. in : Mineralogical and geochemical records of paleoweathering, IGCP 317, Schmitt J.M., Gall Q., (eds), E.N.S.M.P. Mém. Sc. de la Terre, 18, p. 115-132. Widdowson M., 1997, The geomorphological and geological importance of palaeosurfaces. in: Widdowson M. (ed.), Palaeosurfaces: recognition, reconstruction and palaeoenvironmental interpretation. Geol. Soc. Special Publ., 120, p. 1-12.

Chemical and mineralogical analysis of devonian black-shale samples from Martin County, Kentucky; Carroll and Washington counties, Ohio; Wise County, Virginia; and Overton County, Tennessee, U.S.A.

USGS Publications Warehouse

Leventhal, J.S.; Hosterman, J.W.

1982-01-01

Core samples of Devonian shales from five localities in the Appalachian basin have been analyzed chemically and mineralogically. The amounts of major elements are similar; however, the minor constituents, organic C, S, phosphate and carbonate show ten-fold variations in amounts. Trace elements Mo, Ni, Cu, V, Co, U, Zn, Hg, As and Mn show variations in amounts that can be related to the minor constituents. All samples contain major amounts of quartz, illite, two types of mixed-layer clays, and chlorite in differing quantities. Pyrite, calcite, feldspar and kaolinite are also present in many samples in minor amounts. Dolomite, apatite, gypsum, barite, biotite and marcasite are present in a few samples in trace amounts. Trace elements listed above are strongly controlled by organic C with the exception of Mn which is associated with carbonate minerals. Amounts of organic C generally range from 3 to 6%, and S is in the range of 2-5%. Amounts of trace elements show the following general ranges in ppm (parts per million): Co, 20-40; Cu, 40-70; U, 10-40; As, 20-40; V, 150-300; Ni, 80-150; high values are as much as twice these values. The organic C was probably the concentrating agent, and the organic C and sulfide S together created an environment that immobilized and preserved these trace elements. Closely spaced samples showing an abrupt transition in color also show changes in organic C, S and trace-element contents. Several associations exist between mineral and chemical content. Pyrite and marcasite are the only minerals found to contain sulfide-S. In general, the illite-chlorite mixed-layer clay mineral shows covariation with organic C if calcite is not present. The enriched trace elements are not related to the clay types, although the clay and organic matter are intimately associated as the bulk fabric of the rock. ?? 1982.

Diversity of Mineralogy and Occurrences of Phyllosilicates on Mars

NASA Astrophysics Data System (ADS)

Clark, R. N.; Swayze, G. A.; Murchie, S. L.; Mustard, J. F.; Milliken, R. E.; Ehlmann, B. L.; McKeown, N. K.; Calvin, W. M.; Wray, J. J.; Bishop, J. L.

2008-12-01

Minerals and their occurrences tell us about the chemistry, pressure,and temperatures of past environments, and the possible conditions for past habitability. To date, a fair number of phyllosilicates and other minerals have been detected on Mars (e.g., Poulet et al., Nature v438,p623, 2005; Mustard et al., Nature, v454, p309, 2008; Bishop et al., Science, V321, p830, 2008, and references therein). Minerals and amorphous materials detected and mapped over large areas include kaolinite/halloysite, montmorillonite, Fe/Mg-smectite, nontronite, saponite, chlorite, opal/hydrated glass, illite, muscovite, magnesite, prehnite, olivine, high- and low-calcium pyroxene, hematite, jarosite, alunite, kieserite, gypsum, coquimbite or ferricopiapite, possible szomolnokite and others yet to be identified. Phyllosilicate minerals are generally seen associated with Noachian outcrops and are thought to result from aqueous alteration, perhaps over sustained periods. Poly- and mono-hydrated Mg-sulphates appear to have been formed after the phyllosilicates. The patterns and occurrences of minerals so far mapped do not appear to show classic hydrothermal systems as have been observed on Earth (e.g., Yellowstone, Wyoming, and Cuprite, Nevada). Prehnite, previously identified on Mars as scapolite, a low-temperature phyllosilicate commonly found in mafic volcanics on Earth, appears widespread on Mars, often in association with Fe/Mg-smectite or chlorite. Phyllosilicates are observed in local outcrops, but occur regionally, generally indicating the effects of a common alteration process during the Noachian epoch. The discovery of mineralogies indicating both acidic and alkaline environments using CRISM and OMEGA data show that conditions were locally diverse. If the environments for the regional phyllosilicate deposits are found to be hostile to past habitability, perhaps studying the smaller mineralogically diverse areas may prove more fruitful. This talk will review the minerals and their diversity, and geologic environments on Mars and how they compare to terrestrial environments.

A possible source of water in seismogenic subduction zones

NASA Astrophysics Data System (ADS)

Kameda, J.; Yamaguchi, A.; Kimura, G.; Iodp Exp. 322 Scientists

2010-12-01

Recent works on the subduction megathrusts have emphasized the mechanical function of fluids contributing dynamic slip-weakening. Basalt-hosting fault zones in on-land accretionary complexes present several textures of seismic slip under fluid-assisted condition such as implosion breccia with carbonate matrix and decrepitation of fluid inclusion. In order to clarify initiation and evolution processes of such fault zones as well as possible source of fluid in the seismogenic subduction zone, we examined a mineralogical/geochemical feature of basaltic basement recovered by IODP Exp. 322 at C0012, that is a reference site for subduction input in the Nankai Trough. A total of 10 samples (about 4 m depth interval from the basement top) were analyzed in this study. XRD analyses indicate that all of the samples contain considerable amount of smectite. The smectite does not appear as a form of interstratified phase with illite or chlorite. Preliminary chemical analyses by EDS in TEM suggest that the smectite is trioctahedral saponite with Ca as a dominant interlayer cation. To determine the saponite content quantitatively, cation exchange capacity (CEC) of bulk samples was measured. The samples show almost similar CEC of around 30 meq/100g, implying that bulk rock contains about 30 wt% of saponite, considering a general CEC of 100 meq/100g for monomineralic saponite. Such abundance of saponite might be a result from intense alteration of oceanic crust due to sea water circulation at low temperature. Previous experimental work suggests that saponite might be highly hydrated (two to three water layer hydration form) at the seismogenic P-T condition. Hence, altered upper oceanic crust is a possible water sink in the seismogenic zone. The water stored in the smectite interlayer region will be expelled via smectite to chlorite transition reaction, that might contribute to the dynamic weakening of the seimogenic plate boundary between the basement basalt and overlying accretionary prism.

San Rafael, Peru: geology and structure of the worlds richest tin lode

NASA Astrophysics Data System (ADS)

Mlynarczyk, Michael S. J.; Sherlock, Ross L.; Williams-Jones, Anthony E.

2003-08-01

The San Rafael mine exploits an unusually high grade, lode-type Sn-Cu deposit in the Eastern Cordillera of the Peruvian Central Andes. The lode is centered on a shallow-level, Late Oligocene granitoid stock, which was emplaced into early Paleozoic metasedimentary rocks. It has a known vertical extent exceeding 1,200 m and displays marked vertical primary metal zoning, with copper overlying tin. The tin mineralization occurs mainly as cassiterite-quartz-chlorite veins and as cassiterite in breccias. The bulk of it is hosted by a K-feldspar megacrystic, biotite- and cordierite-bearing leucomonzogranite, which is the most distinctive phase of the pluton. Copper mineralization occurs predominantly in the veins that straddle the metasedimentary rock-intrusion contact or are hosted entirely by slates. Both tin and copper mineralization are associated with strong chloritic alteration, which is superimposed on an earlier episode of sericitization and tourmaline-quartz veining. Based on the distribution of alteration and ore mineralogy, cassiterite deposition and subsequent chalcopyrite precipitation are believed to have been the result of a single, prolonged hydrothermal event. The source of the metals is inferred to be a highly evolved, peraluminous magma, related to the leucomonzogranitic phase of the San Rafael pluton. Preliminary fluid inclusion microthermometry suggests that ore deposition took place during the mixing of moderate and low salinity fluids, which were introduced in a series of pulses. Several large fault-jogs, created by sinistral-normal, strike-slip movement, are interpreted to have focused synkinematic magmatic fluids and permitted their effective mixing with meteoric waters. It is proposed that this mixing led to rapid oxidation of Sn (II) chloride species and caused supersaturation of the fluids in cassiterite, resulting in the development of localized, high-grade ore shoots. A favorable structural regime that promoted large-scale mixing of two fluids originating under very different physico-chemical conditions appears to have been the key factor responsible for the unusual richness of the deposit.

Influences of petrographic parameters on technological properties of greywackes used for crushed stone production

NASA Astrophysics Data System (ADS)

Prikryl, Richard; Cermak, Martin; Krutilova, Katerina

2014-05-01

This study focuses on the influence of petrographic parameters on technological properties of greywackes. These sedimentary rocks make about 27 % of crushed stone market in the Czech Republic. Mainly in Moravia (eastern part of the Czech Republic), greywackes represent almost exclusive high quality aggregate. The behaviour of greywackes varies, however, from quarry to quarry. In this study, we have selected the most important deposits that cover major lithological variation of local greywackes. Studied greywackes were analysed for their petrographic parameters quantitatively (using image analysis of thin sections). The pore space characteristics were determined by using fluorescent dye - epoxy resin impregnated specimens. The studied rocks are composed of subangular and angular quartz grains, lithoclasts (stable rocks: quartzites, and unstable rocks: phylites, metaphylites, siltstones, slates, greywackes, and less frequently acid eruptive rocks), feldspars (orthoclas, microcline, plagioclase), and detrital micas. Detrital and authigenic chlorite has been found as well. The matrix which represents the largest volume of rock-forming components contains a mixture of sericite, chlorite, clay minerals, cements, and clasts in aleuropelitic size. Based on the microscopic examination, all studied rock types were classified as greywacke with fine- to medium-grained massive rock fabric. Only specimen from Bělkovice has shown partly layered structure. Alteration of feldspars and unstable rock fragments represents common feature. Diagenetic features included pressure dissolution of quartz clasts and formation of siliceous and/or calcite cements. Based on the experimental study of technological performance of studied greywackes and its correlation to petrographic features, the average size of clasts and volume of matrix make the driving factors affecting the LA values. The LA values decrease with the increasing of volume of matrix (R = 0.61) and with decreasing average grain size (R = 0.44). The degree of sorting influences LA values as well; more graded greywackes tend to show higher LA values. Regarding PSV, its values increase with increasing volume of quartz clasts.

Constraints from geochemistry and oxygen isotopes for the hydrothermal origin of orthoamphibole mafic gneiss in the New Jersey Highlands, north-central Appalachians, USA

NASA Astrophysics Data System (ADS)

Volkert, Richard A.; Peck, William H.

2017-12-01

Rare exposures of orthoamphibole mafic (Oam) gneiss of Mesoproterozoic age in the north-central Appalachians are confined to the northwestern New Jersey Highlands where they form thin lens-shaped bodies composed of gedrite and sparse anthophyllite, oligoclase (An13-An20), biotite, magnetite, and local fluorapatite, rutile, and ilmenite. The gneiss is penetratively foliated and has sharp, conformable contacts against enclosing supracrustal paragneiss and marble. Orthoamphibole mafic gneiss is characterized by low SiO2 (48 ± 2.5 wt%), CaO (1.9 ± 1.3 wt%), and high Al2O3 (18 ± 1.2 wt%), Fe2O3 (10.5 ± 1.6 wt%), and MgO (12 ± 2.3 wt%). Trace element abundances overlap those of unaltered amphibolites in the study area and, coupled with δ18O values of 9.45 ± 0.6‰ (VSMOW) from gedrite separates, support an origin from a basalt protolith. The geochemical and isotopic data are consistent with the formation of Oam gneiss through sea floor hydrothermal alteration of basalt at low temperature of 150-200 °C. Mass-balance calculations indicate gains during alteration mainly in MgO and Al2O3 and losses in CaO, Sr, and light rare earth elements. Our results are compatible with the pre-metamorphic alteration of the basalt protoliths through chloritization and plagioclase dissolution that produced a Mg-rich and Ca-poor rock. Subsequent metamorphism of this chlorite-rich rock to the current mineral assemblage of Oam gneiss took place at ca. 1045 Ma, during the Ottawan phase of the Grenvillian Orogeny. The close spatial association in the study area of Oam gneiss bodies and sulfide occurrences suggests an affinity to the style of mineralization associated with volcanogenic massive sulfide (VMS)-type deposits.

Arsenic release and geochemical evolution of groundwater in an alluvial aquitard, West Bengal, India.

NASA Astrophysics Data System (ADS)

Desbarats, A. J.; Pal, T.; Mukherjee, P. K.; Beckie, R. D.

2017-12-01

According to the World Health Organization, contamination of groundwater by geogenic arsenic (As) represents the largest mass poisoning in history. At a field site in West Bengal, India, the source of As affecting a shallow aquifer was traced to silty sediments filling an abandoned river meander. Along with As-bearing phases, these sediments also contain 0.46 % organic carbon. The release of As within the channel fill is investigated using a geochemical mass balance model supported by detailed field observations of aqueous chemistry, sequential extraction analyses of sediment chemistry, and analyses of sediment mineralogy. The model explores the evolution of groundwater chemistry along a flow path extending from its recharge point in an abandoned channel pond, through the channel-fill sequence, to the underlying aquifer. Variations in groundwater composition within the host sediments are explained in terms of mineral weathering driven by organic carbon decay. The model yields reaction coefficients expressing amounts of minerals (and gases) reacting or precipitating along the flow path. Arsenic and phosphorus cycles appear closely linked as these species are hosted by goethite, Fe-rich chlorite, and vivianite. Arsenic is released through the rapid reductive dissolution of goethite and the slower weathering of chlorite. Concomitantly, some As is sequestered in precipitating vivianite. These competing processes reach equilibrium deeper in the channel-fill sequence as groundwater As concentrations stabilize. Using groundwater residence time in channel fill obtained from a numerical flow model and the calculated reaction coefficients, rates of organic carbon oxidation, goethite dissolution, and net As release are estimated at 1.15 mmol C L-1 a-1, 0.18 mmol L-1 a-1, and 4.57 10-4 mmol L-1 a-1, respectively. Fine-grained yet slightly permeable deposits such as channel-fill silts containing reactive organic carbon and As-bearing goethite and phyllosilicates are localized centers of intense chemical weathering conducive to As mobilization.

Validation of lactic acid bacteria, lactic acid, and acidified sodium chlorite as decontaminating interventions to control Escherichia coli O157:H7 and Salmonella Typhimurium DT 104 in mechanically tenderized and brine-enhanced (nonintact) beef at the purveyor.

PubMed

Echeverry, Alejandro; Brooks, J Chance; Miller, Markus F; Collins, Jesse A; Loneragan, Guy H; Brashears, Mindy M

2010-12-01

After three different outbreaks were linked to the consumption of nonintact meat products contaminated with Escherichia coli O157:H7, the U.S. Food Safety and Inspection Service published notice requiring establishments producing mechanically tenderized and moisture-enhanced beef products to reassess their respective hazard analysis and critical control point systems, due to potential risk to the consumers. The objective of this study was to validate the use of lactic acid bacteria (LAB), acidified sodium chlorite (ASC), and lactic acid (LA) sprays when applied under a simulated purveyor setting as effective interventions to control and reduce E. coli O157:H7 and Salmonella Typhimurium DT 104 in inoculated U.S. Department of Agriculture (USDA) Choice strip loins (longissimus lumborum muscles) pieces intended for either mechanical blade tenderization or injection enhancement with a brine solution after an aging period of 14 or 21 days at 4.4°C under vacuum. After the mechanical process, translocation of E. coli O157:H7 and Salmonella Typhimurium DT 104 from the surface into the internal muscles occurred at levels between 1.00 and 5.72 log CFU/g, compared with controls. LAB and LA reduced internal E. coli O157:H7 loads up to 3.0 log, while ASC reduced the pathogen 1.4 to 2.3 log more than the control (P < 0.05), respectively. Salmonella Typhimurium DT 104 was also reduced internally 1.3 to 2.8, 1.0 to 2.3, and 1.4 to 1.8 log after application of LAB, LA, and ASC, respectively. The application of antimicrobials by purveyors prior to mechanical tenderization or enhancement of steaks should increase the safety of these types of products.

Validation of intervention strategies to control Escherichia coli O157:H7 and Salmonella typhimurium DT 104 in mechanically tenderized and brine-enhanced beef.

PubMed

Echeverry, Alejandro; Brooks, J Chance; Miller, Markus F; Collins, Jesse A; Loneragan, Guy H; Brashears, Mindy M

2009-08-01

After three different outbreaks were linked to the consumption of nonintact meat products contaminated with Escherichia coli O157:H7, the U.S. Department of Agriculture, Food Safety and Inspection Service published notice requiring establishments producing mechanically tenderized and moisture-enhanced beef products to reassess their respective hazard analysis and critical control point system, due to potential risk to the consumers. The purpose of this study was to determine the effectiveness of different intervention strategies (lactic acid, lactic acid bacteria, and acidified sodium chlorite) to control E. coli O157:H7 and Salmonella enterica serotype Typhimurium definitive phage type 104 in mechanically tenderized and brine-enhanced beef strip loins when applied to the steaks prior to packaging and shipment for processing. After the mechanical process, translocation of E. coli O157:H7 and Salmonella Typhimurium DT 104 from the surface into the internal muscles occurred at levels between 2.0 and 4.0 log CFU/g (from an initial inoculation level of 5.0 log) after mechanical tenderization, and at levels of 1.0 to 3.0 log CFU/g after injection, with all the interventions consistently presenting lower microbial counts (P < 0.05) than did the controls. Lactic acid bacteria reduced internal E. coli O157:H7 loads 1.2 to > 2.2 log cycles, while the acidified sodium chlorite and lactic acid reduced them between 0.8 and 3.0 log, respectively. Salmonella Typhimurium DT 104 was also reduced internally after application of all interventions between 0.9 and 2.2 log. The application of antimicrobials to the steaks prior to packaging and shipment on day 0 was effective in reducing internalization of both pathogens in nonintact beef products stored for both 14 and 21 days.

Metasomatic hydration of the Oeyama forearc peridotites: Tectonic implications

NASA Astrophysics Data System (ADS)

Nozaka, Toshio

2014-01-01

In contrast to the widely recognized aspects of serpentinization, initial stages of hydration and tectonic processes of unserpentinized peridotites are still unclear, but have important implications for understanding the lithospheric architecture of supra-subduction zones. This study provides petrological evidence from the Oeyama ophiolite, SW Japan, of the effects of high-temperature metasomatic hydration immediately before the cooling and ductile deformation of forearc peridotites. Key findings in this study are: 1) complex association of high-temperature metasomatic minerals: tremolitic amphibole, cummingtonite, phlogopite, chlorite, olivine and orthopyroxene in veins and in mylonites; 2) the systematic variation in Si and Na + K contents of the tremolitic amphibole, corresponding to its mode of occurrence and mineral association; and 3) the presence of thin (< 0.7 mm) veins of fine-grained olivine accompanied by a narrow diffusion zone of the host primary olivine. On the basis of petrography and mineral chemistry, the temporal sequence of hydration and deformation of the Oeyama ophiolite is considered as follows: 1) infiltration of slab-derived fluids, causing decomposition of primary pyroxene and chemical modification of primary olivine, 2) metasomatic formation of variable modal amounts of amphibole, phlogopite, chlorite, vein-forming olivine and secondary orthopyroxene at 650-750 °C; 3) early-stage mylonitization of the hydrous peridotites in localized shear zones; and 4) syntectonic serpentinization at 400-600 °C to form serpentinite mylonites. Paragenesis and amphibole compositions suggest comparable temperature conditions for metasomatism and early-stage mylonitization. Mylonitization occurred exclusively in hydrous peridotites, and the peridotite mylonites were preferentially overprinted by syntectonic serpentinization. Diffusion profiles of olivine cut by a vein suggest rapid cooling immediately after the metasomatic fluid infiltration. From these observations and calculations, it is concluded that the exhumation of the forearc peridotites was closely related to the infiltration of high-temperature metasomatic fluids and hydration occurred under a wide range of temperature conditions.

Metallogeny of the Mont-de-l'Aigle IOCG deposit, Gaspé Peninsula, Québec, Canada

NASA Astrophysics Data System (ADS)

Simard, M.; Beaudoin, G.; Bernard, J.; Hupé, A.

2006-09-01

The Mont-de-l’Aigle deposit is located in the northern part of Dome Lemieux, in the Connecticut Valley-Gaspé Synclinorium, Gaspé Peninsula, Québec. The Dome Lemieux is a subcircular antiform of Siluro-Devonian sedimentary rocks that is cut by numerous mafic and felsic sills and dikes of Silurian to Late Devonian age. Plutonism occurred in a continental within-plate extensional setting typical of orogenic collapse. The Cu-Fe (± Au) mineralization of Mont-de-l’Aigle occurs in veins, stockworks, and breccias. Mineralization is located near or within N-S and NW-SE faults cutting sedimentary rocks. IOCG mineralization postdates intrusions, skarns, hornfels, and epithermal mineralization typical of the southern part of the Dome Lemieux. The paragenetic sequence comprises: (1) pervasive sodic, potassic, chlorite, and silica alteration, (2) hematite, quartz, pyrite, magnetite, and chalcopyrite veins, stockworks and breccias and, (3) dolomite ± hematite veins and veinlets cutting the earlier mineralization. Intrusions display proximal sodic and potassic alteration, whereas sedimentary rocks have proximal decalcification, silicification, and potassic alteration. Both intrusive and sedimentary rocks are affected by a pervasive distal chlorite (± silica) alteration. The sulfur isotope composition of pyrite and chalcopyrite (δ34S=-1.5 to 4.8‰) suggests that sulfur was derived mainly from igneous rocks. Fluid δ18O (-0.4 to 2.65‰) indicates meteoric or seawater that reacted with the country rocks. Mixing of hot magmatic fluids with a cooler fluid, perhaps meteoric or seawater is suggested for mineral deposition and alteration of the Mont-de-l’Aigle deposit. The mineralogy, alteration, and sulfur isotope composition of the Mont-de-l’Aigle deposit compare well with IOCG deposits worldwide, making the Mont-de-l’Aigle deposit a rare example of Paleozoic IOCG mineralization, formed at shallow depth, within a low metamorphic grade sedimentary rock sequence.

Diagenetic history of the Surma Group sandstones (Miocene) in the Surma Basin, Bangladesh

NASA Astrophysics Data System (ADS)

Rahman, M. Julleh Jalalur; McCann, Tom

2012-02-01

This study examines the various diagenetic controls of the Miocene Surma Group sandstones encountered in petroleum exploration wells from the Surma Basin, which is situated in the northeastern part of the Bengal Basin, Bangladesh. The principal diagenetic minerals/cements in the Surma Group sandstones are Fe-carbonates (with Fe-calcite dominating), quartz overgrowths and authigenic clays (predominantly chlorite, illite-smectite and minor kaolin). The isotopic composition of the carbonate cement revealed a narrow range of δ 18O values (-10.3‰ to -12.4‰) and a wide range of δ 13C value (+1.4‰ to -23.1‰). The δ 13C VPDB and δ 18O VPDB values of the carbonate cements reveal that carbon was most likely derived from the thermal maturation of organic matter during burial, as well as from the dissolution of isolated carbonate clasts and precipitated from mixed marine-meteoric pore waters. The relationship between the intergranular volume (IGV) versus cement volume indicates that compaction played a more significant role than cementation in destroying the primary porosity. However, cementation also played a major role in drastically reducing porosity and permeability in sandstones with poikilotopic, pore-filling blocky cements formed in early to intermediate and deep burial areas. In addition to Fe-carbonate cements, various clay minerals including illite-smectite and chlorite occur as pore-filling and pore-lining authigenic phases. Significant secondary porosity has been generated at depths from 2500 m to 4728 m. The best reservoir rocks found at depths of 2500-3300 m are well sorted, relatively coarse grained; more loosely packed and better rounded sandstones having good porosities (20-30%) and high permeabilities (12-6000 mD). These good quality reservoir rocks are, however, not uniformly distributed and can be considered to be compartmentalized as a result of interbedding with sandstone layers of low to moderate porosities, low permeabilities owing to poor sorting and extensive compaction and cementation.

Hematite (U-Th)/He thermochronometry constrains intraplate strike-slip faulting on the Kuh-e-Faghan Fault, central Iran

NASA Astrophysics Data System (ADS)

Calzolari, Gabriele; Rossetti, Federico; Ault, Alexis K.; Lucci, Federico; Olivetti, Valerio; Nozaem, Reza

2018-03-01

The Kuh-e-Faghan strike-slip fault system (KFF), located to the northern edge of the Lut Block in central Iran, developed through a Neogene-Quaternary pulsed history of eastward fault propagation and fault-related exhumation. This system is a consequence of the residual stresses transmitted from the Arabia-Eurasia convergent plate boundary. Here we integrate structural and textural analysis with new and previously published apatite fission-track (AFT) and apatite (U-Th)/He (apatite He) results, chlorite thermomentry, and hematite (U-Th)/He data from hematite-coated brittle fault surfaces to constrain the timing of tectonic activity and refine patterns of late Miocene-Pliocene burial and exhumation associated with the propagation of the KFF. Twenty-nine hematite (U-Th)/He (hematite He) dates from three striated hematite coated slip surfaces from the KFF fault core and damage zone yield individual dates from 12-2 Ma. Petrographic analysis and chlorite thermometry of a polyphase, fossil fluid system in the KFF fault core document that fluid circulation and mineralization transitioned from a closed system characterized by pressure solution and calcite growth to an open system characterized by hot hydrothermal (T = 239 ± 10 °C) fluids and hematite formation. Hematite microtextures and grain size analysis reveal primary and secondary syntectonic hematite fabrics, no evidence of hematite comminution and similar hematite He closure temperatures ( 60-85 °C) in each sample. Integration of these results with thermal history modeling of AFT and apatite He data shows that KFF activity in the late Miocene is characterized by an early stage of fault nucleation, fluid circulation, hematite mineralization, and eastward propagation not associated with vertical movement that lasted from 12 to 7 Ma. Hematite He, AFT, and apatite He data track a second phase of fault system activity involving fault-related exhumation initiating at 7 Ma and continuing until present time. Our new data constrain the onset of the recognized Late Miocene-Pliocene tectonic reorganization in north-central Iran.

Types and Mechanisms of Alterations on the Mesozoic Ophiolites (Lake Van Region-Turkey): Petrographical and Geochemical Approach

NASA Astrophysics Data System (ADS)

Yazıcı, Ömer; Üner, Tijen; Mutlu, Sacit; Depçi, Tolga

2017-04-01

Mesozoic ophiolites are widely located in the eastern part of Lake Van Basin. The ophiolitic rocks deformed during the rifting and/or closure period of the Neo-Tethyan Ocean are observed as tectonic slices in the region. These ophiolites are represented by volcano-sedimentary units, isolated dikes, and mafic-ultramafic rocks. The formation, emplacement and post-emplacement processes of these ophiolitic rocks can be understood owing to alterations as rodingitization, serpentinization, and listwaenitization. Three stages of sequent mineralization are detected in the ophiolitic rocks. First stage is pyrometasomatization, represented by metamorphic minerals (garnet, chlorite etc.), observed in intruded dikes. Second stage is hydrothermal alteration of mafic-ultramafic rocks namely serpentinization. Listwaenite alteration is the last stage of mineralization. According to petrographical investigations, garnet+chlorite+diopsite minerals are detected in rodengites. The conversion of the plagioclase minerals to the calcsilicatic minerals in rodengites suggests that these rocks are metasomatic rocks produced by Ca-rich fluids derived from serpentinization of the ultramafic rocks. The serpentine minerals (chrysotile-lizardite) can be distinguished from each other by their morphology as being platy or fibrous. Listwaenite alteration is followed by the formation of carbonate, silica, oxides and hydroxides. Chemical analysis of these rocks show that the listwaenites have an enrichment in Ni and Co contents while the rodingites have low SiO2 and high CaO and MgO values (SiO2 28,50 - 36,67%, CaO 11,99 - 20,88%, and MgO 7,99 - 17,73%). Alteration types observed on the ophiolitic rocks demonstrate that these rocks are metamorphised by low pressure and low to middle temperature conditions (greenshist facies). Serpentinization is pointing out an alteration which occurred during the emplacement of the ophiolites or the latter period. This study has been supported by Project number 2013-FBE-YL072 of the Department of Scientific Research Projects of Yüzüncü Yıl University.

Co-evolution of monsoonal precipitation in East Asia and the tropical Pacific ENSO system since 2.36 Ma: New insights from high-resolution clay mineral records in the West Philippine Sea

NASA Astrophysics Data System (ADS)

Yu, Zhaojie; Wan, Shiming; Colin, Christophe; Yan, Hong; Bonneau, Lucile; Liu, Zhifei; Song, Lina; Sun, Hanjie; Xu, Zhaokai; Jiang, Xuejun; Li, Anchun; Li, Tiegang

2016-07-01

Clay mineralogical analysis and scanning electron microscope (SEM) analysis were performed on deep-sea sediments cored on the Benham Rise (core MD06-3050) in order to reconstruct long-term evolution of East Asian Summer Monsoon (EASM) rainfall in the period since 2.36 Ma. Clay mineralogical variations are due to changes in the ratios of smectite, which derive from weathering of volcanic rocks in Luzon Island during intervals of intensive monsoon rainfall, and illite- and chlorite-rich dusts, which are transported from East Asia by winds associated with the East Asian Winter Monsoon (EAWM). Since Luzon is the main source of smectite to the Benham Rise, long-term consistent variations in the smectite/(illite + chlorite) ratio in core MD06-3050 as well as ODP site 1146 in the Northern South China Sea suggest that minor contributions of eolian dust played a role in the variability of this mineralogical ratio and indicate strengthening EASM precipitation in SE Asia during time intervals from 2360 to 1900 kyr, 1200 to 600 kyr, and after 200 kyr. The EASM rainfall record displays a 30 kyr periodicity suggesting the influence of El Niño-Southern Oscillation (ENSO). These intervals of rainfall intensification on Luzon Island are coeval with a reduction in precipitation over central China and an increase in zonal SST gradient in the equatorial Pacific Ocean, implying a reinforcement of La Niña-like conditions. In contrast, periods of reduced rainfall on Luzon Island are associated with higher precipitation in central China and a weakening zonal SST gradient in the equatorial Pacific Ocean, thereby suggesting the development of dominant El Niño-like conditions. Our study, therefore, highlights for the first time a long-term temporal and spatial co-evolution of monsoonal precipitation in East Asia and of the tropical Pacific ENSO system over the past 2.36 Ma.

Spatial and mineralogic variation of Na-Ca alteration in Laramide porphyry systems of Arizona

NASA Astrophysics Data System (ADS)

Runyon, S.; Seedorff, E.; Barton, M. D.; Mazdab, F. K.; Lecumberri-Sanchez, P.; Steele-MacInnis, M.

2017-12-01

Na-Ca alteration is characterized by the metasomatic addition of Ca ± Na and the loss of K. Minor volumes of Na-Ca alteration in Laramide porphyry systems develops from 3 to 8 km paleodepth. Mineral assemblages, mineral compositions, hydrogen isotopes, whole-rock analyses, and reconnaissance fluid inclusion characteristics have been documented for Na-Ca alteration in Laramide porphyry systems such as Tea Cup and Sierrita. Volumetrically minor Na-Ca alteration in Laramide porphyry systems documented in this study commonly takes the form of one of three mineral assemblages: albite-epidote-chlorite, Na-plagioclase-actinolite ± epidote, and garnet- or diopside-stable Na-plagioclase-actinolite ± epidote. These different Na-Ca mineral assemblages have broad spatial relationships, from shallow albite-chlorite-epidote to deeper Na-plagioclase-actinolite within a given district. Hydrogen isotope data on Na-Ca alteration minerals shows consistently distinct δD compositions of Na-Ca alteration minerals compared to igneous minerals in a given district. Further, calculated hydrogen isotope composition of fluids in equilibrium with Na-Ca alteration minerals are consistently enriched in δD compared to magmatic-hydrothermal fluids. Whole-rock analyses show consistent losses of K and variable addition of Na and Ca across different Na-Ca alteration assemblages. Na-Ca alteration has been well documented associated with the Jurassic arc. Previous studies demonstrated through mass balance, timing and spatial relationships, isotopic, and fluid inclusion studies that Na-Ca alteration associated with the Jurassic arc likely formed from the circulation of external, highly saline, non-magmatic fluids (e.g., Battles and Barton, 1995; Dilles et al., 1995). Na-Ca alteration documented in Laramide systems is generally similar to Na-Ca alteration documented along the Jurassic arc in mineral assemblages, compositions, and timing, but the volume of Na-Ca alteration in the Laramide systems is small as compared to the voluminous Na-Ca alteration documented in systems associated with the Jurassic arc.

Ore deposits and epithermal evidences associated with intra-magmatic faults at Aïn El Araâr-Oued Belif ring structure (NW of Tunisia)

NASA Astrophysics Data System (ADS)

Aissa, Wiem Ben; Aissa, Lassaâd Ben; Amara, Abdesslem Ben Haj; Tlig, Said; Alouani, Rabah

2017-03-01

Hydrothermal ore deposits at Aïn El Araâr-Oued Belif location are classified as epithermal deposits type. The ore bodies are hosted by upper Turonian (8-9 M.y) volcanic rhyodacitic complex. Polymetallic sulfide orebodies are mainly concentrated within intra-magmatic faults. Petrographic, XRD, and TEM-STEM investigations revealed that ore minerals are essentially, arsenopyrite, pyrite, chalcopyrite, pyrrhotite, hematite, goethite and magnetite with Au, Ag and Pt trace metals. Gangue minerals are mainly adularia, quartz, sericite, alunite, tridymite, chlorite, phlogopite and smectite. Epithermal alteration is well zoned with four successive characteristic zones: (1) zone of quartz-adularia-sericite and rare alunite; (2) zone of kaolinite and plagioclase albitization; (3) intermediate zone of illite-sericite; (4) sapropelic alteration type zone of chlorite-smectite and rare illite. This can be interpreted as a telescoping of two different acidity epithermal phases; low sulfidation (adularia-sericite) and high sulfidation (quartz-alunite), separated in time or due to a gradual increase of fluids acidity and oxicity within the same mineralization phase. Brecciated macroscopic facies with fragments hosting quartz-adularia-sericite minerals (low-sulfidation phase) without alunite, support the last hypothesis. Geodynamic context and mineral alteration patterns are closely similar to those of Maria Josefa gold mine at SE of Spain which exhibit a volcanic-hosted epithermal ore deposit in a similar vein system, within rhyolitic ignimbrites, altered to an argillic assemblage (illite-sericite abundant and subordinate kaolinite) that grades outwards into propylitic alteration (Sanger-von Oepen et al. (1990)). Mineralogical and lithologic study undertaken in the volcanic host rock at Aïn El Araâr-Oued Belif reveals a typical epithermal low-sulfidation and high-sulfidation ore deposits with dominance of low-sulfidation. Host rocks in these systems range from silicic to intermediate for adularia-sericite type (low sulfidation) to rhyodacite for quartz-alunite type (high sulfidation).

Experimental Evaluation of pH and Temperature Effects on the Adsorption of Boron onto Clay Minerals

NASA Astrophysics Data System (ADS)

Hoenisch, B.; Marone, D.; Ruprecht, J.

2017-12-01

Modeling the secular evolution of the concentration [B] and isotopic composition (δ11B) of boron in seawater is hampered by limited constraints on the relative sources (i.e. riverine input of weathering products, hydrothermal convection at mid-ocean ridges and fluids expelled from accretionary prisms) and sinks (i.e. alteration of the oceanic crust, adsorption onto clays, and co-precipitation in carbonates) of boron to and from the ocean. Clays remove approximately 28% of total boron from the ocean and quantification of this sink thus represents a major factor for reconstructing the secular evolution of seawater [B] and δ11B over the Cenozoic. However, the relative strength of the clay sink could have been much smaller in the early Cenozoic compared to today, because borate ion as the charged species is preferentially adsorbed onto detrital clays over boric acid, and because the relative abundance of borate in seawater should have been lower under the more acidic conditions of the early Cenozoic. In addition, different clay minerals tend to fractionate boron isotopes differentially, and the relative composition of clay minerals has varied in the past with the dominant climate and weathering patterns on the continents. We have conducted a range of pH (7.5-8.4) and temperature (3-32°C) experiments with four clay minerals (Kaolinite, Illite, Montmorillonite and Chlorite), to build on previously published but limited experimental data. Similar to a previous study and as expected based on the relative abundance of borate ion in seawater, boron adsorption onto these clays increases at higher pH and lower temperatures, but whereas Montmorillonite and Illite absorb similar quantities of boron, Kaolinite is most and Chlorite least efficient in this process. We are now in the process of characterizing the boron isotope fractionation associated with these adsorption experiments.

Syntectonic fluid flux during rift faulting: Record from the MIS core, Victoria Land Basin, Antarctica

NASA Astrophysics Data System (ADS)

Millan, C.; Wilson, T. J.; Paulsen, T. S.

2009-12-01

The McMurdo Ice Shelf project successfully recovered 1285 m of Neogene sedimentary core from the Victoria Land Basin, a large rift basin within the West Antarctic Rift System (WARS) of Antarctica. The core contains 1475 natural fractures that were logged as faults, veins and clastic dikes, associated with the southern extension of the Neogene-active? Terror Rift fault zone. Veins constitute about 625 of this population. Most veins are filled with calcite, although zeolites and minor chlorite are common towards the bottom of the core. In the lower ~300 m of the core, veins contain opening-mode fiber fills and are wavy to tightly folded due to vertical shortening. Folded, opening-mode folded veins are filled by calcite fibers that grew normal to vein walls, indicating the host sediment was cohesive enough to fracture but was not fully lithified and accommodated vein buckling during compaction. Fold hinges are fractured and wedging of vein segments is marked by overlapping tips separated by zones with strong chlorite and clay fabrics, suggesting shearing during further vertical contraction of the host rock. Calcite veins are commonly strongly twinned. Cathodoluminescence microscopy shows minor changes in color and intensity and minimal concentric or sectoral zoning, suggesting relatively rapid crystallization of fluids of similar chemistry. However, stable isotope analyses reveal large variations in values, with carbon values ranging from -21.91 to -7.15 (VPBD) and oxygen values ranging from -5.35 to -11.97 (VPBD). Further detailed investigation of the fracture fills using cathodoluminescence and electron microscopy combined with isotopic analysis of carbon and oxygen will document the generations of the filling material in more detail and will constrain the sources and evolution of the fluids. There has clearly been significant structural control on fluid pathways during lithification, compaction and diagenesis of strata deforming within the Terror Rift zone.

Characterization and origin of spongillite-hosting sediment from João Pinheiro, Minas Gerais, Brazil

NASA Astrophysics Data System (ADS)

Almeida, A. C. S.; Varajão, A. F. D. C.; Gomes, N. S.; Varajão, C. A. C.; Volkmer-Ribeiro, C.

2010-03-01

Spongillite from João Pinheiro, Minas Gerais, Brazil is mainly known for its use in brick production and in the refractory industry. Very few studies have focused on its geological context. Spongillite-rich deposits occur in shallow ponds on a karstic planation surface developed on rocks of the Neoproterozoic São Francisco Supergroup. Cenozoic siliciclastic sediments are related to this surface. A field study of these deposits and analysis of multispectral images showed a SE-NW preferential drainage system at SE, suggesting that Mesozoic Areado Group sandstones were the source area of the spongillite-hosting sediments. Mineralogical and textural characterization by optical microscopic analysis, X-ray diffraction (XRD), differential and gravimetric thermal analysis (DTA-GTA), infrared spectroscopy (IR) and scanning electron microscopy (SEM) of seven open-pit spongillite-rich deposits (Avião, Carvoeiro, Vânio, Preguiça, Divisa, Severino, Feijão) showed a sedimentological similarity between the deposits. They are lens-shaped and are characterized at the bottom by sand facies, in the middle by spicules-rich muddy-sand facies and at the top by organic matter-rich muddy-sand facies. Petrographically, the spongillite-hosting sediments and the siliclastic sediments of the Areado Group show detrital phases with similar mineralogical and textural features, such as the presence of well-sorted quartz grains and surface features of abrasion typical of aeolian reworking that occurred in the depositional environment in which the sandstones of the Areado Group were formed. Detrital heavy minerals, such as staurolite, zircon, tourmaline, and clay minerals, such as kaolinite, low amounts of illite, scarce chlorite and mixed-layer chlorite/smectite and illite/smectite occur in the spongillite-hosting sediments and in sandstones from the Areado Group. In both formations, staurolite has similar chemical composition. These mineralogical and textural features show that the sediments of the Areado Group constitute the main source of the pond sediments that host spongillite.

Listvenite formation from peridotite: Insights from Oman Drilling Project hole BT1B and preliminary reaction path model approach.

NASA Astrophysics Data System (ADS)

de Obeso, J. C.; Kelemen, P. B.; Manning, C. E.; Michibayashi, K.; Harris, M.

2017-12-01

Oman Drilling Project hole BT1B drilled 300 meters through the basal thrust of the Samail ophiolite. The first 200 meters of this hole are dominated by listvenites (completely carbonated peridotites) and serpentinites. Below 200 meters the hole is mainly composed of metasediments and metavolcanics. This core provides a unique record of interaction between (a) mantle peridotite in the leading edge of the mantle wedge and (b) hydrous, CO2 rich fluids derived from subducting lithologies similar to those in the metamorphic sole. We used EQ3/6 to simulate a reaction path in which hydrous fluid in equilibrium with qtz + calcite + feldspar + chlorite or smectite reacts with initially fresh peridotite at 100°C (the estimated temperature of alteration, Falk & Kelemen GCA 2015) and 5 kb. Water was first equilibrated with minerals observed during core description in the metamorphic sole at 100°C and 5kb. This fluid is then reacted with olivine enstatite and diopside (Mg#90) approximating the average composition of residual mantle peridotite (harzburgite) in Oman. Secondary minerals resulting from complete reaction are then reacted again with the initial fluid in an iterative process, up to water/rock > 1000. Water/rock close to 1 results in complete serpentinization of the peridotite, with chrysotile, brucite and magnetite as the only minerals. Water/rock >10 produces carbonates, chlorite and talc. Further increasing water/rock to > 100 produces assemblages dominated by carbonates and quartz with minor muscovite, similar to listvenites of hole BT1B that contain qtz + carbonates + Fe-oxyhydroxides + relict spinel ± chromian muscovite and fuchsite. The results of this preliminary model are consistent with the complex veining history of core from BT1B, with carbonate/iron oxide veins in both listvenites and serpentinites interpreted to be the earliest record of peridotite carbonation after initial serpentinization.

Geochemical models of metasomatism in ultramafic systems: Serpentinization, rodingitization, and sea floor carbonate chimney precipitation

USGS Publications Warehouse

Palandri, J.L.; Reed, M.H.

2004-01-01

In a series of water-rock reaction simulations, we assess the processes of serpentinization of harzburgite and related calcium metasomatism resulting in rodingite-type alteration, and seafloor carbonate chimney precipitation. At temperatures from 25 to 300??C (P = 10 to 100 bar), using either fresh water or seawater, serpentinization simulations produce an assemblage commonly observed in natural systems, dominated by serpentine, magnetite, and brucite. The reacted waters in the simulations show similar trends in composition with decreasing water-rock ratios, becoming hyper-alkaline and strongly reducing, with increased dissolved calcium. At 25??C and w/r less than ???32, conditions are sufficiently reducing to yield H2 gas, nickel-iron alloy and native copper. Hyperalkalinity results from OH- production by olivine and pyroxene dissolution in the absence of counterbalancing OH- consumption by alteration mineral precipitation except at very high pH; at moderate pH there are no stable calcium minerals and only a small amount of chlorite forms, limited by aluminum, thus allowing Mg2+ and Ca2+ to accumulate in the aqueous phase in exchange for H+. The reducing conditions result from oxidation of ferrous iron in olivine and pyroxene to ferric iron in magnetite. Trace metals are computed to be nearly insoluble below 300??C, except for mercury, for which high pH stabilizes aqueous and gaseous Hg??. In serpentinization by seawater at 300??C, Ag, Au, Pd, and Pt may approach ore-forming concentrations in sulfide complexes. Simulated mixing of the fluid derived from serpentinization with cold seawater produces a mineral assemblage dominated by calcite, similar to recently discovered submarine, ultramafic rock-hosted, carbonate mineral deposits precipitating at hydrothermal vents. Simulated reaction of gabbroic or basaltic rocks with the hyperalkaline calcium- and aluminum-rich fluid produced during serpentinization at 300??C yields rodingite-type mineral assemblages, including grossular, clinozoisite, vesuvianite, prehnite, chlorite, and diopside. ?? 2004 Elsevier Ltd.

P-T and structural constraints of lawsonite and epidote blueschists from Liberty Creek and Seldovia: Tectonic implications for early stages of subduction along the southern Alaska convergent margin

NASA Astrophysics Data System (ADS)

López-Carmona, Alicia; Kusky, Timothy M.; Santosh, M.; Abati, Jacobo

2011-01-01

The southern Alaska convergent margin contains several small belts of sedimentary and volcanic rocks metamorphosed to blueschist facies, located along the Border Ranges fault on the contact between the Wrangellia and Chugach terranes. These belts are significant in that they are the most inboard, and thus probably contain the oldest record of Triassic-Jurassic northward-directed subduction beneath Wrangellia. The Liberty Creek HP-LT schist belt is the oldest and the innermost section of the Chugach terrane. Within this belt lawsonite blueschists contains an initial high-pressure assemblage formed by lawsonite + phengite + chlorite + sphene + albite ± apatite ± carbonates and quartz. Epidote blueschists are composed of sodic, sodic-calcic and calcic amphiboles + epidote + phengite + chlorite + albite + sphene ± carbonates and quartz. P-T pseudosections computed from four representative samples constrain maximum pressures at 16 kbar and 250-280 °C for the Lawsonite-bearing blueschists, and 15 kbar and 400-500 °C for the epidote-bearing blueschists, suggesting a initial subduction stage of 50-55 km depth. The growth of late albite porphyroblasts in all samples suggests a dramatic decompression from ca. 9 kbar to 5 kbar. The Liberty Creek schists can be correlated with the Seldovia blueschist belt on the Kenai Peninsula. Metamorphism in both terranes took place in the Early Jurassic (191-192 Ma), recording an early stage of subduction beneath Wrangellia. In the nearby terranes of the same margin, the age of metamorphism records an early stage of subduction at 230 Ma. Based on this difference in age, a maximum of 40 Ma were necessary to subduct the protoliths of the Seldovia and Liberty Creek blueschists to depths of circa 50-55 km, suggesting a minimum vertical component of subduction of 1.2-1.5 cm/year.

Mass change calculations of hydrothermal alterations within the volcanogenic metasediments hosted Cu-Pb (-Zn) mineralization at Halilar area, NW Turkey

NASA Astrophysics Data System (ADS)

Kiran Yildirim, Demet; Abdelnasser, Amr; Doner, Zeynep; Kumral, Mustafa

2016-04-01

The Halilar Cu-Pb (-Zn) mineralization that is formed in the volcanogenic metasediments of Bagcagiz Formation at Balikesir province, NW Turkey, represents locally vein-type deposit as well as restricted to fault gouge zone directed NE-SW along with the lower boundary of Bagcagiz Formation and Duztarla granitic intrusion in the study area. Furthermore, This granite is traversed by numerous mineralized sheeted vein systems, which locally transgress into the surrounding metasediments. Therefore, this mineralization closely associated with intense hydrothermal alteration within brecciation, and quartz stockwork veining. The ore mineral assemblage includes chalcopyrite, galena, and some sphalerite with covellite and goethite formed during three phases of mineralization (pre-ore, main ore, and supergene) within an abundant gangue of quartz and calcite. The geologic and field relationships, petrographic and mineralogical studies reveal two alteration zones occurred with the Cu-Pb (-Zn) mineralization along the contact between the Bagcagiz Formation and Duztarla granite; pervasive phyllic alteration (quartz, sericite, and pyrite), and selective propylitic alteration (albite, calcite, epidote, sericite and/or chlorite). This work, by using the mass balance calculations, reports the mass/volume changes (gain and loss) of the chemical components of the hydrothermal alteration zones associated with Halilar Cu-Pb (-Zn) mineralization at Balikesir area (Turkey). It revealed that the phyllic alteration has enrichments of Si, Fe, K, Ba, and LOI with depletion of Mg, Ca, and Na reflect sericitization of alkali feldspar and destruction of ferromagnesian minerals. This zone has high Cu and Pb with Zn contents represents the main mineralized zone. On the other hand, the propylitic zone is characterized by addition of Ca, Na, K, Ti, P, and Ba with LOI and Cu (lower content) referring to the replacement of plagioclase and ferromagnesian minerals by albite, calcite, epidote, and sericite with chlorite. Keywords: Mass balance calculations; hydrothermal alterations; Cu-Pb (-Zn) mineralization; Halilar area; NW Turkey

Dissolution-precipitation creep at mid-crustal levels of the Scandian Caledonides: the COSC-1 case study

NASA Astrophysics Data System (ADS)

Giuntoli, Francesco; Menegon, Luca; Warren, Clare

2017-04-01

The thermo-mechanical properties of the middle and lower crust exert a fundamental control on the structure of orogenic belts, and on the amount and style of shortening during continental collision. By virtue of the deep erosional level, the internal parts of the Scandinavian Caledonides expose middle and lower crustal sections involved in subduction-exhumation history and nappe stacking. In this study we analysed the development of a mylonitic microstructure and the associated deformation mechanisms in amphibolites from the middle portion (1.5-2.2 km of depth) of the COSC-1 drill core, central Sweden. Mylonitic amphibolites are common in the drill core. They are composed of hornblende, plagioclase, chlorite, quartz, epidote, carbonate and ilmenite. The plagioclase displays two generations: (1) fractured millimetric porphyroclast cores (Plag1; Ab 99), which are wrapped by the foliation and are dark in the SEM-cathodoluminescence images, and (2) rims (Plag2; Ab 80-90), some tens of microns in size, are bright in the cathodoluminescence images, heal the fractures and overgrow the cores of Plag1. Plag2 grows syn-deformationally, as it is commonly found in strain shadows around Plag1 porphyroclasts. The hornblende preserves corroded cores (Amp1) with higher Mg number compared to the rims (Amp2). The Amp2 is lengthened as the foliation and shows intergrowths with Plag2 and chlorite in strain shadows. Amphibole crystals are commonly boudinaged parallel to the foliation, with chlorite filling the boudin necks. Preliminary pressure and temperature estimates, using Amp2 and Plag2 pairs, constrain their growth at 600°C and 1GPa. EBSD analysis indicates a homogeneous orientation of the porphyroclastic Plag1 without the development of low-angle boundaries, suggesting that Plag1 crystals are strain free. Furthermore, the fractures are sealed by the Plag2 with the same crystallographic orientation as the plagioclase core. The Plag2 grains have their [100] axes oriented subparallel to the stretching lineation, but they are also internally strain free. Thus, we interpret the CPO of Plag2 as a result of oriented grain growth during dissolution-precipitation creep. The enrichment of Ca in Plag2 could reflect either a difference in the PT conditions compared to the growth of Plag1 or a possible metasomatic event characterized by an influx of a Ca-rich fluid, as suggested by the presence of intergranular calcite crystals as well as discrete calcite veins. The X-ray chemical maps and the EBSD maps suggest that (micro)cracking and dissolution- precipitation creep were responsible for the development of the mylonitic amphibolites, and that crystal plasticity was not a dominant deformation mechanism, although deformation occurred at pressure and temperature conditions at which plagioclase is expected to deform by dislocation creep. In conclusion, in middle crustal levels the presence of water at the grain boundaries enhances chemical reaction and is responsible for deformation through dissolution and precipitation processes that create a strong preferred crystallographic orientation in the newly grown minerals.

A-type and I-type granitoids and mylonitic granites of Hassan Salaran area of SE Saqqez, Kurdistan, Iran

NASA Astrophysics Data System (ADS)

Abdullah, Fakhraddin Mohammad; Saeed Ahmad, Sheler

2014-05-01

The Hassan Salarn area is located 20km to southeast of Saqqez city in Kurdistan Province, western Iran. In this area there are two distinct granitic rock suites consisting A-type and I-type granites and also mylonitic granites. These A-type and I-type granites have various petrological and geochemical characteristics. They also have different origins and petrogenesis. A-type granitoids comprise alkali feldspar granite, syenogranite and quartz alkali feldspar syenite, whereas I-type granitoids are composed of monzogranite, granodiorite and tonalite. Geochemically, A-type granitoids are peralkaline and acmite-normative but I-type granitoids are subalkaline (calc-alkaline), metaluminous and diopside-normative. A-type granitoids are also ferroan alkali and ferroan alkali-calcic whereas I-type granitoids are magnesian and calcic. A-type granitoids resemble to within plate granites and post-orogenic granites whereas I-type granitoids resemble to volcanic arc granites. A-type granitoids contain higher concentrations of alkalies, Zr, Rb, Nb, Y, Th, Ce, high FeO/MgO ratios and lower concentrations of Mg, Ca and Sr, resembling post-orogenic A-type granites. It is possible that heat from a mantle-derived magma which intruded into the lower crust, and/or rapid crustal extension have been essential generation of approriate melts producing A-type granitoids. Thus we can conclude that A-type granitoids were generated from a mixed mantle-crust source. Negative Nb anomalies and low contents of Ti and P probably indicate a subduction-related origin for protolith of I-type granitoids. Negative Nb anomalies and enrichment in Ce relative to its adjacent elements can be related to involvement of continental crust in magmatic processes. I-type granitoids are also enriched in Rb, Ba, K, Th, Ce and depleted in Nb, Zr and Y, indicating that they have had interacted with crust. I-type granitoids may result from contamination of mantle-derived magmas by continental crust during a subduction event. The mylonitic granites are elongated masses with a NE-SW trend and their contacts with the A-type and I-type granitoids are fault contact. Hand specimens have a layered appearance with green bands made from chlorite and epidote and grey to white bands with quartz and feldspar. These rocks contain plagioclase, quartz and orthoclase under the microscope. Also fine-grained minerals such as quartz, sericite, epidote, chlorite and opaque minerals make the groundmass wrapping the porphyroclasts. Pressure shadows around porphyroclasts of plagioclase and quartz and crystallization of fine-grained quartz and sericite in these places along with intense alteration of plagioclase to epidote and sericite, existence of quartz with different sizes, andaluse extinction in quartz crystals, and elongation of chlorites, resulted from dynamic recrystallisation of biotites all indicate effect of stresses on the rocks. Considering the similar mineralogical composition of the mylonitic rocks with I-type granitoid, it could be concluded that the granodioritic magma, after intrusion and solidification, is changed to mylonite in a shear zone due to tectonical forces.

Geologic and mineralogic controls on acid and metal-rich rock drainage in an alpine watershed, Handcart Gulch, Colorado

USGS Publications Warehouse

Bove, Dana J.; Caine, Jonathan S.; Lowers, Heather

2012-01-01

The surface and subsurface geology, hydrothermal alteration, and mineralogy of the Handcart Gulch area was studied using map and drill core data as part of a multidisciplinary approach to understand the hydrology and affects of geology on acid-rock drainage in a mineralized alpine watershed. Handcart Gulch was the locus of intense hydrothermal alteration that affected an area of nearly 3 square kilometers. Hydrothermal alteration and accompanied weak mineralization are spatially and genetically associated with small dacite to low-silica rhyolite stocks and plugs emplaced about 37-36 Ma. Felsic lithologies are commonly altered to a quartz-sericite-pyrite mineral assemblage at the surface, but alteration is more variable in the subsurface, ranging from quartz-sericite-pyrite-dominant in upper core sections to a propylitic variant that is more typical in deeper drill core intervals. Late-stage, hydrothermal argillic alteration [kaolinite and(or) smectite] was superimposed over earlier-formed alteration assemblages in the felsic rocks. Smectite in this late stage assemblage is mostly neoformed resulting from dissolution of chlorite, plagioclase, and minor illite in more weakly altered rocks. Hydrothermally altered amphibolites are characterized by biotitic alteration of amphibole, and subsequent alteration of both primary and secondary biotite to chlorite. Whereas pyrite is present both as disseminations and in small veinlets in the felsic lithologies, it is mostly restricted to small veinlets in the amphibolites. Base-metal sulfides including molybdenite, chalcopyrite, sphalerite, and galena are present in minor to trace amounts in the altered rocks. However, geologic data in conjunction with water geochemical studies indicate that copper mineralization may be present in unknown abundance in two distinct areas. The altered rocks contain an average of 8 weight percent fine pyrite that is largely devoid of metals in the crystal structure, which can be a significant source of trace metals in other areas with acid rock drainage. Thus, elevated base-metal concentrations in the trunk stream and discrete springs in the study area, as determined in previous studies, are likely derived from discrete metal-rich sources, rather than the abundant pyrite veins or disseminations. Pyrite is oxidized in nearly all outcrops examined. Drill core data show that zones of pyrite oxidation range in depth from 100 meters below the surface at higher elevations to just a few meters depth at the lowest elevations in the study area. However, discrete pyrite oxidation zones are present in drill core to depths of several hundred meters below the pervasive near-surface oxidation zones. These deeper discrete oxidation zones, which are present where fresh pyrite predominates, are spatially associated with fractures, small faults, and breccias. Quartz-sericite-pyrite-altered rocks containing unoxidized pyrite likely have the highest acid-generating capacity of all alteration assemblages in the study area. Hydrothermal alteration has left these rocks base-cation leached and thus acid-neutralizing potential is negligible. In contrast, propylitic-altered felsic rocks commonly contain trace to minor calcite and abundant chlorite, which provide some amount of acid-neutralization despite the presence of a few percent pyrite.

Lower Paleozoic Through Archean Detrital Zircon Ages From Metasedimentary Rocks of the Nome Group, Seward Peninsula, Alaska

NASA Astrophysics Data System (ADS)

Amato, J. M.; Miller, E. L.; Gehrels, G.

2003-12-01

Metamorphic rocks of Seward Peninsula have been divided into two groups based on their metamorphic grade and history: The Nome Group and the Kigluaik Group. Although it is sometime been assumed that the higher structural position of the Nome Group versus the Kigluaik Group indicates the Kigluaik Group is older, this relationship and the age of the protoliths of these rocks has never been well-established. The Nome Group includes (delete the) lower grade blueschist and greenschist facies rocks which are widespread across the Seward Peninsula (delete) Rock types include pelitic schist, more mafic chlorite-white mica-albite schist, marble, quartzite, and metabasite. An early metamorphic event (pre-120 Ma) occurred at high pressure and relatively low temperature, and is everywhere overprinted by younger deformation and greenschist facies Rare eclogite facies assemblages are preserved in metabasites, and garnet-glaucophane in some of the pelitic schists. The Kigluaik Group includes upper greenschist to granulite facies rocks that are exposed in the core of a gneiss dome. They record a younger event (~91 Ma) that occurred at higher temperatures and resulted in partial thermal overprinting of the Nome Group and upper greenschist to granulite facies assemblages forming in the Kigluaik Group. The Kigluaik Group and equivalent rocks in the Bendeleben and Darby Mountains represent at least in part similar protoliths to many of the units in the Nome Group (Till and Dumoulin, 1994). The boundary between the rocks of the Nome Group and those clearly affected by the second metamorphic event is placed arbitrarily at the "Biotite-in" isograd along the flanks of the gneiss dome. In order to assess the protolith ages and source rock ages for these units, detrital zircon ages were obtained from three samples from the Nome Group, with Kigluaik Group ages forthcoming. LA-MC-ICPMS U/Pb isotope analysis was used for dating. Two samples were collected from the western Kigluaik Mountains near Eldorado Creek and one further south along the Feather River. Each sample yielded 90-105 analyses and all uncertainties are 1 sigma. Chlorite schist MC-74 has a range of ages from the two youngest grains at 484 +/- 18 Ma and 510 +/- 7 Ma to 2984 +/- 2 Ma. Chlorite schist LMC-30 has a youngest grain at 521 +/- 2 Ma and an oldest grain of 2027 +/- 12. Quartz-mica schist LMC-58 also has a youngest grain at 521 +/- 2 Ma and an oldest grain of 2655 +/- 7 Ma. All three therefore have lower Paleozoic zircons, suggesting Lower Cambrian or younger depositional ages. Combining the data from all three rocks results in peaks on a cumulative probability plot at (in descending order of importance): 600 Ma, 683 Ma, 1593 Ma, 522 Ma, and 2985 Ma, with several smaller peaks between 774-1540 Ma and 1685-1960 Ma. Published ages from Nome Group orthogneisses are 680 Ma, suggesting the samples so far analyzed are likely in part sourced from local basement rocks that were eroded to provide ~680 Ma detrital zircons to sedimentary protoliths of part of the Nome Group.

Bioreduction of Fe-bearing clay minerals and their reactivity toward pertechnetate (Tc-99)

DOE Office of Scientific and Technical Information (OSTI.GOV)

Bishop, Michael E.; Dong, Hailiang; Kukkadapu, Ravi K.

2011-07-01

99Technetium (99Tc) is a fission product of uranium-235 and plutonium-239 and poses a high environmental hazard due to its long half-life (t1/2 = 2.13 x 105 y), abundance in nuclear wastes, and environmental mobility under oxidizing conditions [i.e., Tc(VII)]. Under reducing conditions, Tc(VII) can be reduced to insoluble Tc(IV). Ferrous iron [Fe(II)], either in aqueous form or in mineral form, has been used to reduce Tc(VII) to Tc(IV). However, the reactivity of Fe(II) from clay minerals, other than nontronite, toward immobilization of Tc(VII) and its role in retention of reduced Tc(IV) have not been investigated. In this study the reactivitymore » of a suite of clay minerals toward Tc(VII) reduction and immobilization was evaluated. The clay minerals chosen for this study included five members in the smectite-illite (S-I) series, (montmorillonite, nontronite, rectorite, mixed layered I-S, and illite), chlorite, and palygorskite. Fe-oxides were removed from these minerals with a modified dithionite-citrate-bicarbonate (DCB) procedure. The total Fe content of these clay minerals, after Fe-oxide removal, ranged from 0.7 to 30.4% by weight, and the Fe(III)/Fe(total) ratio ranged from 44.9 to 98.5%. X-ray diffraction (XRD) and Mössbauer spectroscopy results showed that after Fe oxide removal the clay minerals were free of Fe-oxides. Scanning electron microscopy (SEM) revealed that little dissolution occurred during the DCB treatment. Bioreduction experiments were performed in bicarbonate buffer (pH-7) with Fe(III) in the clay minerals as the sole electron acceptor, lactate as the sole electron donor, and Shewanella Putrifaciens CN32 cells as mediators. In select tubes, anthraquinone-2,6-disulfate (AQDS) was added as electron shuttle to facilitate electron transfer. The extent of Fe(III) bioreduction was the highest for chlorite (~43 wt%) and the lowest for palygorskite (~4.17 wt%). In the S-I series, NAu-2 was the most reducible (~31 %) and illite the least (~0.4 %). The extent and initial rate of bioreduction were positively correlated with the percent smectite in the S-I series (i.e., layer expandability). Fe(II) in the bioreduced clay minerals subsequently was used to reduce Tc(VII) to Tc(IV) in PIPES buffer. Similar to the trend of bioreduction, in the S-I series, reduced smectite showed the highest reactivity toward Tc(VII), and reduced illite exhibited the least. The initial rate of Tc(VII) reduction, after normalization to clay and Fe(II) concentrations, was positively correlated with the percent smectite in the S-I series. Fe(II) in chlorite and palygorskite was also reactive toward Tc(VII) reduction. These data demonstrate that crystal chemical parameters (layer expandability, Fe and Fe(II) contents, and surface area etc.) play important roles in controlling the extent and rate of bioreduction and the reactivity toward Tc(VII) reduction. Reduced Tc(IV) resides within clay mineral matrix, and this association could minimize any potential of reoxidation over long term.« less

Celestine-bearing geodes from Wayne and Emery counties, southeastern Utah: Genesis and mineralogy

USGS Publications Warehouse

Kile, Daniel E.; Dayvault, Richard D.; Hood, William C.; Hatch, H. Steven

2015-01-01

Geodes containing celestine with associated quartz, calcite, chlorite, and other minerals occur in the Jurassic Curtis Formation of Emery and Wayne counties off the east and south flanks of the San Rafael Swell in southeastern Utah. The two areas discussed in this article produce geodes to 25 cm wide containing bladed to tabular celestine crystals that are as much as 4.5 cm in length. An evaporative littoral system resulting in the formation of anhydrite nodules is proposed as the initial environment for this deposit. Subsequent silicification of the nodules and, in some cases, the formation of hollow spaces within the silicified nodules, provided a geode structure for the eventual crystallization of celestine and associated minerals.

Alteration of Al-rich inclusions inside amoeboid olivine aggregates in the Allende meteorite

NASA Technical Reports Server (NTRS)

Hashimoto, Akihiko; Grossman, Lawrence

1987-01-01

The primary phases of Al-rich inclusions in amoeboid olivine aggregates have undergone alteration reactions with the solar nebular gas. The simplest interpretation of the present observations is that melilite was the first primary phase to disappear with falling temperature, and was replaced by grossular + anorthite + feldspathoids, followed by fassaite; spinel was the last phase to be altered. Thermodynamic calculations suggest that Na-rich phlogopite could have formed at about 470 K and chlorite at about 328 K at a water fugacity of 0.000001, which is that of a gas of solar composition in this temperature range. The olivine around Al-rich inclusions is not serpentized, indicating the cessation of gas-solid equilibrium above 274 K.

Contact Electrification of Regolith Particles and Chloride Electrolysis: Synthesis of Perchlorates on Mars.

PubMed

Tennakone, K

2016-10-01

Contact electrification of chloride-impregnated martian regolith particles due to eolian agitation and moisture condensation on coalesced oppositely charged grains may lead to spontaneous electrolysis that generates hypochlorite, chlorite, chlorate, and perchlorate with a concomitant reduction of water to hydrogen. This process is not curtailed even if moisture condenses as ice because chloride ionizes on the surface of ice. Limitations dictated by potentials needed for electrolysis and breakdown electric fields enable estimation of the required regolith grain size. The estimated dimension turns out to be of the same order of magnitude as the expected median size of martian regolith, and a simple calculation yields the optimum rate of perchlorate production. Key Words: Mars oxidants-Perchlorate-Dust electrification-Electrolysis. Astrobiology 16, 811-816.

Analysis of mixed-layer clay mineral structures

USGS Publications Warehouse

Bradley, W.F.

1953-01-01

Among the enormously abundant natural occurrences of clay minerals, many examples are encountered in which no single specific crystallization scheme extends through a single ultimate grain. The characterization of such assemblages becomes an analysis of the distribution of matter within such grains, rather than the simple identification of mineral species. It having become established that the particular coordination complex typified by mica is a common component of many natural subcrystalline assemblages, the opportunity is afforded to analyze scattering from random associations of these complexes with other structural units. Successful analyses have been made of mixed hydration states of montmorillonite, of montmorillonite with mica, of vermiculite with mica, and of montmorillonite with chlorite, all of which are variants of the mica complex, and of halloysite with hydrated halloysite.

Le volcanisme cambrien du Maroc central : implications géodynamiquesThe Central Morocco Cambrian volcanism: geodynamic implications

NASA Astrophysics Data System (ADS)

Ouali, Houssa; Briand, Bernard; Bouchardon, Jean-Luc; Capiez, Paul

2003-05-01

In southeastern Central Morocco, the Bou-Acila volcanic complex is considered of Cambrian age. In spite of low-grade metamorphic effect, initial volcanic texture and mineralogy can be recognized and volcanic rocks are dominated by dolerites and porphyric dolerites. The initial mineralogy is composed of plagioclases, pyroxenes and dark minerals. A secondary mineral assemblage is composed of albite, epidote, chlorite and calcite. According to their immobile elements compositions, the southeastern central Morocco metavolcanites are of within-plate continental tholeiites. This volcanism and those recognized in many other areas in Morocco confirm a Cambrian extensive episode within the Gondwana supercontinent. To cite this article: H. Ouali et al., C. R. Geoscience 335 (2003).To cite this article: H. Ouali et al., C. R. Geoscience 335 (2003).

Mineralogy of a mudstone at Yellowknife Bay, Gale crater, Mars.

PubMed

Vaniman, D T; Bish, D L; Ming, D W; Bristow, T F; Morris, R V; Blake, D F; Chipera, S J; Morrison, S M; Treiman, A H; Rampe, E B; Rice, M; Achilles, C N; Grotzinger, J P; McLennan, S M; Williams, J; Bell, J F; Newsom, H E; Downs, R T; Maurice, S; Sarrazin, P; Yen, A S; Morookian, J M; Farmer, J D; Stack, K; Milliken, R E; Ehlmann, B L; Sumner, D Y; Berger, G; Crisp, J A; Hurowitz, J A; Anderson, R; Des Marais, D J; Stolper, E M; Edgett, K S; Gupta, S; Spanovich, N

2014-01-24

Sedimentary rocks at Yellowknife Bay (Gale crater) on Mars include mudstone sampled by the Curiosity rover. The samples, John Klein and Cumberland, contain detrital basaltic minerals, calcium sulfates, iron oxide or hydroxides, iron sulfides, amorphous material, and trioctahedral smectites. The John Klein smectite has basal spacing of ~10 angstroms, indicating little interlayer hydration. The Cumberland smectite has basal spacing at both ~13.2 and ~10 angstroms. The larger spacing suggests a partially chloritized interlayer or interlayer magnesium or calcium facilitating H2O retention. Basaltic minerals in the mudstone are similar to those in nearby eolian deposits. However, the mudstone has far less Fe-forsterite, possibly lost with formation of smectite plus magnetite. Late Noachian/Early Hesperian or younger age indicates that clay mineral formation on Mars extended beyond Noachian time.

Parametric spatiotemporal oscillation in reaction-diffusion systems.

PubMed

Ghosh, Shyamolina; Ray, Deb Shankar

2016-03-01

We consider a reaction-diffusion system in a homogeneous stable steady state. On perturbation by a time-dependent sinusoidal forcing of a suitable scaling parameter the system exhibits parametric spatiotemporal instability beyond a critical threshold frequency. We have formulated a general scheme to calculate the threshold condition for oscillation and the range of unstable spatial modes lying within a V-shaped region reminiscent of Arnold's tongue. Full numerical simulations show that depending on the specificity of nonlinearity of the models, the instability may result in time-periodic stationary patterns in the form of standing clusters or spatially localized breathing patterns with characteristic wavelengths. Our theoretical analysis of the parametric oscillation in reaction-diffusion system is corroborated by full numerical simulation of two well-known chemical dynamical models: chlorite-iodine-malonic acid and Briggs-Rauscher reactions.

Evidence of Phyllosilicate in Wooly Patch+: An Altered Rock Encountered on the Spirit Rover Traverse

NASA Technical Reports Server (NTRS)

Wang, Alian; Haskin, Larry A.; Korotev, Randy L.; Jolliff, Brad L.; deSouza, Paulo, Jr.; Kusack, Alastair G.

2005-01-01

In the course of examining rocks along the traverse of the Spirit rover toward the Columbia Hills [1, 9], we noticed that the chemistry of a rock named "Wooly Patch" was neither basaltic as the rocks near the landing site [8] nor slightly altered basalt inferred from regolith in plains trenches [10]. The major cation ratios appear to match those of phyllosilicates [11]. The presence of phyllosilicate minerals on Mars has been predicted [12]; reasons for the rarity or absence of phyllosilicates have also been discussed [13]. We have thus done as detailed an analysis of Wooly Patch as the data enable, which suggests phyllosilicates of kaolinite, serpentine, and chlorite types, plus some feldspar and pyroxene are prime candidates to constitute Wooly Patch.

A study of the depth of weathering and its relationship to the mechanical properties of near-surface rocks in the Mojave Desert

USGS Publications Warehouse

Stierman, D.J.; Healy, J.H.

1985-01-01

Weathered granite extends 70 m deep at Hi Vista in the arid central Mojave Desert of southern California. The low strength of this granite is due to the alteration of biotite and chlorite montmorillonite. Deep weathering probably occurs in most granites, although we cannot rule out some anomalous mechanisms at Hi Vista. Geophysical instruments set in these slightly altered rocks are limited by the unstable behavior of the rocks. Thus, tectonic signals from instruments placed in shallow boreholes give vague results. Geophysical measurements of these weathered rocks resemble measurements of granitic rocks near major faults. The rheology of the rocks in which instruments are placed limits the useful sensitivity of the instruments. ?? 1985 Birkha??user Verlag.

Parametric spatiotemporal oscillation in reaction-diffusion systems

NASA Astrophysics Data System (ADS)

Ghosh, Shyamolina; Ray, Deb Shankar

2016-03-01

We consider a reaction-diffusion system in a homogeneous stable steady state. On perturbation by a time-dependent sinusoidal forcing of a suitable scaling parameter the system exhibits parametric spatiotemporal instability beyond a critical threshold frequency. We have formulated a general scheme to calculate the threshold condition for oscillation and the range of unstable spatial modes lying within a V-shaped region reminiscent of Arnold's tongue. Full numerical simulations show that depending on the specificity of nonlinearity of the models, the instability may result in time-periodic stationary patterns in the form of standing clusters or spatially localized breathing patterns with characteristic wavelengths. Our theoretical analysis of the parametric oscillation in reaction-diffusion system is corroborated by full numerical simulation of two well-known chemical dynamical models: chlorite-iodine-malonic acid and Briggs-Rauscher reactions.

A method for the concentration of fine-grained rutile (TiO2) from sediment and sedimentary rocks by chemical leaching

USGS Publications Warehouse

Commeau, Judith A.; Valentine, Page C.

1991-01-01

Most of the sample analyzed by the method described were marine muds collected from the Gulf of Maine (Valentine and Commeau, 1990). The silt and clay fraction (up to 99 wt% of the sediment) is composed of clay minerals (chiefly illite-mica and chlorite), silt-size quartz and feldspar, and small crystals (2-12 um) of rutile and hematite. The bulk sediment samples contained an average of 2 to 3 wt percent CaCO3. Tiher samples analyzed include red and gray Carboniferous and Triassic sandstones and siltstones exposed around the Bay of Fundy region and Paleozoic sandstones, siltstones, and shales from northern Maine and New Brunswick. These rocks are probable sources for the fine-grained rutile found in the Gulf of Maine.

Geology of the Cupsuptic quadrangle, Maine

USGS Publications Warehouse

Harwood, David S.

1966-01-01

The Cupsuptic quadrangle, in west-central Maine, lies in a relatively narrow belt of pre-Silurian rocks extending from the Connecticut River valley across northern New Hampshire to north-central Maine. The Albee Formation, composed of green, purple, and black phyllite with interbedded-quartzite, is exposed in the core of a regional anticlinorium overlain to the southeast by greenstone of the Oquossoc Formation which in turn is overlain by black slate of the Kamankeag Formation. In the northern part of the quadrangle the Albee Formation is overlain by black slate, feldspathic graywacke, and minor greenstone of the Dixville Formation. The Kamankeag Formation is dated as 1-ate Middle Ordovician by graptolites (zone 12) found near the base of the unit. The Dixville Formation is correlated with the Kamankeag Formation and Oquossoc Formation and is considered to be Middle Ordovician. The Albee Formation is considered to be Middle to Lower Ordovician from correlations with similar rocks in northeastern and southwestern Vermont. The Oquossoc and Kamankeag Formations are correlated with the Amonoosuc and Partridge Formations of northern New Hampshire. The pre-Silurian rocks are unconformably overlain by unnamed rocks of Silurian age in the southeast, west-central, and northwest ninths of the quadrangle. The basal Silurian units are boulder to cobble polymict conglomerate and quartz-pebble conglomerate of late Lower Silurian (Upper Llandovery) age. The overlying rocks are either well-bedded slate and quartzite, silty limestone, or arenaceous limestone. Thearenaceous limestone contains Upper Silurian (Lower Ludlow) brachiopods. The stratified rocks have been intruded by three stocks of biotite-muscovite quartz monzonite, a large body of metadiorite and associated serpentinite, smaller bodies of gabbro, granodiorite, and intrusive felsite, as well as numerous diabase and quartz monzonite dikes. The metadiorite and serpentinite, and possibly the gabbro and granodiorite are Late Ordovician in age. The quartz monzonite is considered to be Late Devonian. Five tectonic events are inferred from the structural features in the area. The earliest was a period of folding producing tightly-appressed, northeast-trending folds in the rocks of pre-Silurian age. In the second stage the folded pre-Silurian rocks were uplifted, eroded, and truncated to produce a major unconformity between the Middle Ordovician and Lower Silurian rocks. These events constitute the Taconic orogeny. The third tectonic event was a period of folding, probably of Middle Devonian age, that warped the unconformity and overlying rocks into open, gently-plunging, east-trending folds. This period of folding undoubtedly changed the attitude of the early folds in the pre-Silurian units but it did not produce any recognizable, cross-cutting planar features in the older rocks. The fourth tectonic event was a period of igneous intrusion that locally deformed the northeast-trending folds in the pre-Silurian rocks into a macroscopic drag fold plunging at 80 degrees in a direction S.10?w. A north-trending, subvertical slip cleavage was produced locally during this period of Late Devonian (?) deformation. A period of faulting, possibly of Triassic age, dislocated some of the earlier features. The rocks are in the chlorite zone of regional metamorphism, but have been contact metamorphosed to sillimanite-bearing hornfels adjacent to the quartz monzonite stocks. The chemical changes in chlorite, biotite, garnet, cordierite, and muscovite in the chlorite, biotite, andalusite, and sillimanite zones have been-studied by optical and x-ray methods and by partial chemical analyses. The progressive changes in mineral assemblages have been graphically portrayed on quaternary diagrams and ternary projections.

Poly-phase Deformation Recorded in the Core of the Coast Plutonic Complex, Western British Columbia

NASA Astrophysics Data System (ADS)

Hamblock, J. M.; Andronicos, C. L.; Hurtado, J. M.

2006-05-01

The Coast Plutonic Complex of western British Columbia constitutes the largest batholith within the North American Cordillera. The field area for this study is Mt. Gamsby, an unexplored region above the Kitlope River, east of the Coast Shear Zone and at the southern end of the Central Gneiss Complex. The dominant lithologies on Mt. Gamsby include amphibolite and metasedimentary gneiss, gabbro-diorite, and orthogneiss. The amphibolite gneiss contains alternating amphibolite and felsic layers, with chlorite and epidote pervasive in some regions and garnet rare. This unit is commonly migmatized and contains various folds, boudins, and shear zones. The metasedimentary gneiss contains quartz, k-spar, graphite, chlorite, and perhaps cordierite, but appears to lack muscovite and aluminosilicates. The gabbro-diorite is salt and pepper in color and contains ca. 50% pyroxene and plagioclase. The orthogneiss is light in color and plagioclase-rich, with a texture varying from coarse-grained and undeformed to mylonitic. In some regions, this unit contains abundant mafic enclaves. At least four deformational events (D1-4) are observed. The second generation of folding, F2, is dominant in the area and resulted in the production of a large synform during sinistral shearing. The S1 foliation is observed only in the amphibolite gneiss and is orthogonal to S2, creating mushroom- type fold interference patterns. S2 foliations strike NW-SE and dip steeply to the SW, suggesting SW-NE directed shortening. L2 lineations developed on S2 plunge shallowly to the NW and SE, implying strike-slip motion. Although both dextral and sinistral motions are indicated by shear band data, sinistral motion is dominant. The average right and left lateral shear band orientation is nearly identical to S2, suggesting that right and left lateral shearing were synchronous. Foliations within the orthogneiss are parallel to the axes of S2 folds and boudins in the amphibolite gneiss, suggesting that emplacement of orthogneiss was concurrent with S2 deformation of the amphibolite gneiss. Tectonic strains calculated by the Rf-φ method using mafic enclaves in the orthogneiss vary from 4 to 10 within an area <1 km2, suggesting strong strain gradients during D2. S3 foliations strike WNW-ESE to E-W and dip shallowly to the south, suggesting NNE-SSW to N-S shortening. L3 lineations plunge shallowly to the SW and SE, and are associated low-angle shear bands with greenschist facies mineral assemblages which overprint higher temperature assemblages. Deformation phase D4 is characterized by low temperature, brittle deformation as shown by discrete fault surfaces with abundant chlorite. The following tectonic history can be determined based on structural observations. Amphibolite and immature sedimentary material formed from supracrustal (e.g. basalt flows?) and intrusive protoliths. These units were then intruded by the gabbro- diorite, which was deformed by right and left lateral shear zones sometime after crystallization. Both the amphibolite and gabbro-diorite were intruded by the orthogneiss, which was emplaced as sills during right and left lateral shearing and F2 folding. This geologic history is similar to that preserved in other parts of the Coast Plutonic Complex where dextral transpression and sinistral transtension are documented. The localization of low angle normal shear zones with greenschist facies mineral assemblages suggests extension occurred during cooling of the arc.

Fluid-related modifications of Cr-spinel and olivine from ophiolitic peridotites by contact metamorphism of granitic intrusions in the Ablah area, Saudi Arabia

NASA Astrophysics Data System (ADS)

Ahmed, Ahmed Hassan; Surour, Adel Abdullah

2016-05-01

The Ablah serpentinized peridotites and overlying layered metagabbros represent an allochthonous piece of a dismembered ophiolite in the southern Hijaz terrane that belongs to the Neoproterozoic Arabian Shield in Saudi Arabia. On both sides, the ophiolite is bounded by wider domains of granitic intrusions and volcano-sedimentary successions, all together follow a N-S trend. The protolith of the Ablah serpentinized peridotites is mainly harzburgite which is partly or totally serpentinized. Carbonate veins of variable sizes invade and hydrate the serpentinized peridotites. Away from the contact with the granitic intrusions, fresh primary (igneous) olivine and Cr-spinel are preserved in the partly serpentinized peridotites. These relict primary minerals are used to infer their tectonic setting of formation as a nascent spreading center rock association of mid-ocean ridge or back-arc basin setting. Based on the re-distribution of elements related to different thermal effects, three patterns of Cr-spinel modification can be defined. The first pattern can be followed in the partly serpentinized peridotites where Cr-spinel displays simple zoning that is characterized by sharp contact between primary Al-rich cores and secondary Fe3+-rich rims. These cores and rims are homogeneous and show progressive decrease in Mg, Al and Cr, but with remarkable increase in Fe3+ and Fe2+ toward the rims. Mineral assemblage in equilibrium with this type of Cr-spinel is primary olivine + antigorite + chlorite ± talc ± chrysotile. The second pattern of Cr-spinel modification is represented by homogeneous weakly zoned Cr-rich spinel with no distinct sharp contacts between Cr-rich cores and magnetite rims. Cr-spinel cores of this type are rich in Cr and Fe2+, and poor in Mg, Al and Fe3+. The mineral assemblage in equilibrium with this Cr-spinel type is Fe-rich olivine + antigorite + enstatite + chlorite + tremolite + anthophyllite ± talc. The third pattern is defined by pervasive heterogeneous modification in which the alteration starts from the cores outwards forming a very characteristic "atoll" textured SiO2- and Cr-rich porous spinel. This type is characterized by core-to-rim increase in Cr, Fe3+, Si, Mn, Ni and Ti, and decrease in Mg, Al and Fe2+. The mineral assemblage in equilibrium with this pattern is chlorite + carbonates + lizardite/chrysotile ± antigorite. The first modification pattern is suggested to form under nearly solid-state conditions in the distal part from the granitic intrusion. The second pattern could be formed under reducing conditions with high temperature and fluid/rock ratio near the contact zone. The peak metamorphic temperature of this stage ranges from 500 to 650 °C that indicate upper amphibolite facies conditions. During retrograde metamorphism, the hydrothermal fluids are cooler and oxidizing which lead to the precipitation of thick marble-like carbonate veins within the serpentinized peridotites. In such a case, the aqueous fluids attack the Al- and Mg-rich cores, which are less resistant and replicable than the Fe-rich rims, and form the third chemical modification pattern of porous SiO2-rich spinel. The high SiO2 content in Cr-spinel is most probably attributed to the formation of Mg- and Al-rich silicates within the sub-microscopic pores of altered Cr-spinel.

Geology and porphyry copper-type alteration-mineralization of igneous rocks at the Christmas Mine, Gila County, Arizona

USGS Publications Warehouse

Koski, Randolph A.

1979-01-01

The Christmas copper deposit, located in southern Gila County, Arizona, is part of the major porphyry copper province of southwestern North America. Although Christmas is known for skarn deposits in Paleozoic carbonate rocks, ore-grade porphyry-type copper mineralization also occurs in a composite granodioritic intrusive complex and adjacent mafic volcanic country rocks. This study considers the nature, distribution, and genesis of alteration-mineralization in the igneous rock environment at Christmas. At the southeast end of the Dripping Spring Mountains, the Pennsylvanian Naco Limestone is unconformably overlain by the Cretaceous Williamson Canyon Volcanics, a westward-thinning sequence of basaltic volcanic breccia and lava flows, and subordinate clastic sedimentary rocks. Paleozoic and Mesozoic strata are intruded by Laramide-age dikes, sills, and small stocks of hornblende andesite porphyry and hornblende rhyodacite porphyry, and the mineralized Christmas intrusive complex. Rocks of the elongate Christmas stock, intruded along an east-northeast-trending fracture zone, are grouped into early, veined quartz diorite (Dark Phase), biotite granodiorite porphyry (Light Phase), and granodiorite; and late, unveined dacite porphyry and granodiorite porphyry. Biotite rhyodacite porphyry dikes extending east and west from the vicinity of the stock are probably coeval with biotite granodiorite porphyry. Accumulated normal displacement of approximately 1 km along the northwest-trending Christmas-Joker fault system has juxtaposed contrasting levels (lower, intrusive-carbonate rock environment and upper, intrusive-volcanic rock environment) within the porphyry copper system. K-Ar age determinations and whole-rock chemical analyses of the major intrusive rock types indicate that Laramide calc-alkaline magmatism and ore deposition at Christmas evolved over an extended period from within the Late Cretaceous (~75-80 m.y. ago) to early Paleocene (~63-61 m.y. ago). The sequence of igneous rocks is progressively more alkaline and silicic from basalt to granodiorite. Early (Stage I) chalcopyrite-bornite (-molybdenite) mineralization and genetically related K-silicate alteration are centered on the Christmas stock. K-silicate alteration is manifested by pervasive hornblende-destructive biotitization in the stock, biotitization of basaltic volcanic wall rocks, and a continuous stockwork of K-feldspar veinlets and quartz-K-feldspar veins in the stock and quartz-sulfide veins in volcanic rocks. Younger (Stage II) pyrite-chalcopyrite mineralization and quartz-sericite-chlorite alteration occur in a zone overlapping with but largely peripheral to the zone of Stage I stockwork veins. Within the Christmas intrusive complex, K-silicate-altered rocks in the central stock are flanked east and west by zones of fracture-controlled quartz-sericite alteration and strong pyritization. In volcanic rocks quartz-chlorite-pyrite-chalcopyrite veins are superimposed on earlier biotitization and crosscut Stage I quartz-sulfide veins. Beyond the zones of quartz-sericite alteration, biotite rhyodacite porphyry dikes contain the propylitic alteration assemblage epidote-chlorite-albite-sphene. Chemical analyses indicate the following changes during pervasive alteration of igneous rocks: (1) addition of Si, K, H, S, and Cu, and loss of Fe 3+ and Ca during intense biotitization of basalt; (2) loss of Na and Ca, increase of Fe3+/Fe2+, and strong H-metasomatism during sericitization of quartz diorite; and (3) increase in Ca, Na, and Fe3+/Fe2+, and loss of K during intense propylitization of biotite rhyodacite porphyry dikes. Thorough biotitization of biotite granodiorite porphyry in the Christmas stock was largely an isochemical process. Fluid-inclusion petrography reveals that Stage I veins are characterized by low to moderate populations of moderate-salinity and gas-rich inclusions, and sparse but ubiquitous halite-bearing inclusions. Moderate-salinity an

Geochemical, microtextural and petrological studies of the Samba prospect in the Zambian Copperbelt basement: a metamorphosed Palaeoproterozoic porphyry Cu deposit.

NASA Astrophysics Data System (ADS)

Master, Sharad; Mirrander Ndhlovu, N.

2015-04-01

Ever since Wakefield (1978, IMM Trans., B87, 43-52) described a porphyry-type meta-morphosed Cu prospect, the ca 50 Mt, 0.5% Cu Samba deposit (12.717°S, 27.833°E), hosted by porphyry-associated quartz-sericite-biotite schists in northern Zambia, there has been controversy about its origin and significance. This is because it is situated in the basement to the world's largest stratabound sediment-hosted copper province, the Central African Copperbelt, which is hosted by rocks of the Neoproterozoic Katanga Supergroup. Mineralization in the pre-Katangan basement has long played a prominent role in ore genetic models, with some authors suggesting that basement Cu mineralization may have been recycled into the Katangan basin through erosion and redeposition, while others have suggested that the circulation of fluids through Cu-rich basement may have leached out the metals which are found concentrated in the Katangan orebodies. On the basis of ca 490-460 Ma Ar-Ar ages, Hitzman et al. (2012, Sillitoe Vol., SEG Spec. Publ., 16, 487-514) suggested that Samba represents late-stage impregnation of copper mineralization into the basement, and that it was one of the youngest copper deposits known in the Central African Copperbelt. If the Samba deposit really is that young, then it would have post-dated regional deformation and metamorphism (560-510 Ma), and it ought to be undeformed and unmetamorphosed. The Samba mineralization consists of chalcopyrite and bornite, occurring as disseminations, stringers and veinlets, found in a zone >1 km along strike, in steeply-dipping lenses up to 10m thick and >150m deep. Our new major and trace element XRF geochemical data (14 samples) show that the host rocks are mainly calc-alkaline metadacites. Cu is correlated with Ag (Cu/Ag ~10,000:1) with no Au or Mo. Our study focused on the microtextures and petrology of the Samba ores. We confirm that there is alteration of similar style to that accompanying classical porphyry Cu mineralization, including potassic (biotite+sericite+ quartz), propylitic (clinozoisite+chlorite+saussuritized plagioclase), phyllic (sericite+quartz+ pyrite+hydromuscovite/illite) and argillic (kaolinite+chlorite+dolomite) alteration. The clays were identified with XRD. All the rocks show penetrative deformational textures and fabrics. Our textural studies show that phyllic zone pyrite crystals have quartz-rich pressure shadows, and they predate all phases of deformation. Similarly, in the potassic zone, fracture-controlled biotite stringers in particular orientations are deformed, and partly replaced by chlorite, again showing their pre-deformational, pre-metamorphic origin. Copper sulfide-bearing quartz veinlets are deformed. Many of the alteration assemblages containing biotite or sericite have been deformed into crenulated schists, showing that they were formed early in the deformation history. Coupled with the dating of a Samba metavolcanic rock at 1964±12 Ma (Rainaud et al., 2005, JAES, 42, 1-31), we regard the Samba deposit as a metamorphosed Palaeoproterozoic porphyry-type Cu deposit, which has undergone deformation, and retrograde metamorphism of its alteration assemblages, during the Neoproterozoic Lufilian Orogeny, followed by post-tectonic cooling, which occurred throughout the Copperbelt at about 480±20 Ma. Samba, together with the Mkushi deposits, is part of a long-lived (>100 Ma) Palaeoproterozoic porphyry-Cu province in the Zambian Copperbelt basement, and ore genetic theories for the Copperbelt mineralization must now seriously take this into account.

Clay minerals, metallic oxides and oxy-hydroxides and soil organic carbon distribution within soil aggregates in temperate forest soils

NASA Astrophysics Data System (ADS)

Gartzia-Bengoetxea, Nahia; Fernández-Ugalde, Oihane; Virto, Iñigo; Arias-González, Ander

2017-04-01

Soil mineralogy is of primary importance for key environmental services provided by soils like carbon sequestration. However, current knowledge on the effects of clay mineralogy on soil organic carbon (SOC) stabilization is based on limited and conflicting data. In this study, we investigated the relationship between clay minerals, metallic oxides and oxy-hydroxides and SOC distribution within soil aggregates in mature Pinus radiata D.Don forest plantations. Nine forest stands located in the same geographical area of the Basque Country (North of Spain) were selected. These stands were planted on different parent material (3 on each of the following: sandstone, basalt and trachyte). There were no significant differences in climate and forest management among them. Moreover, soils under these plantations presented similar content of clay particles. We determined bulk SOC storage, clay mineralogy, the content of Fe-Si-Al-oxides and oxyhydroxides and the distribution of organic C in different soil aggregate sizes at different soil depths (0-5 cm and 5-20 cm). The relationship between SOC and abiotic factors was investigated using a factor analysis (PCA) followed by stepwise regression analysis. Soils developed on sandstone showed significantly lower concentration of SOC (29 g C kg-1) than soils developed on basalts (97 g C kg-1) and trachytes (119 g C kg-1). The soils on sandstone presented a mixed clay mineralogy dominated by illite, with lesser amounts of hydroxivermiculite, hydrobiotite and kaolinite, and a total absence of interstratified chlorite/vermiculite. In contrast, the major crystalline clay mineral identified in the soils developed on volcanic rocks was interstratified chlorite/vermiculite. Nevertheless, no major differences were observed between basaltic and trachytic soils in the clay mineralogy. The selective extraction of Fe showed that the oxalate extractable iron was significantly lower in soils on sandstone (3.7%) than on basalts (11.2%) and trachytes (8.2%) with no significant differences between the last two. On the other hand, ditionithe extractable iron was significantly different among all soils with the following content: sandstone (13%) < trachytes (23%) < basalts (27%). Short-range order inorganic phases of Al and Fe were significantly higher in soils developed on volcanic parent materials. The distribution of organic C in soil aggregates revealed that as much as 50% of the organic C was concentrated in mega (20-10 mm and 10-5 mm) and large-(5-2 mm) aggregates in soils developed in sandstones, while 25% and 36% of the total organic C was found in theses aggregates in basaltic and trachytic soils respectively. Basaltic soils showed significantly higher proportion of organic C (>20%) in microaggregates (0.25-0.053 mm) and silt+clay size aggregates (< 0.053 mm) than the other two soils (<10%). The regression analysis revealed that short-range order minerals influence the amount of SOC via microaggregation and that chlorite-vermiculite mixed layer minerals had a significant influence on the amount of SOC relating this stabilization mechanism to macroagregation. This study highlights that dynamic models of SOC turnover in acid soils from temperate forest should include proxies for clay mineralogy and for the content of Fe and Al oxides and oxy-hydro-oxides.

Origins of chromite and magnetite in sedimentary rocks deposited in a shallow water environment in the 3.2 Ga Moodies Group, South Africa

NASA Astrophysics Data System (ADS)

Otake, T.; Sakamoto, Y.; Itoh, S.; Yurimoto, H.; Kakegawa, T.

2012-12-01

*Otake, T. totake@eng.hokudai.ac.jp Div. of Sustainable Resources Engineering, Hokkaido Univ., Sapporo, Japan Sakamoto, Y. yu.sakamoto12@gmail.com Dep. of Earth Science, Tohoku Univ., Sendai, Japan Itoh, S. sitoh@ep.sci.hokudai.ac.jp Dep. of Natural History Sciences, Hokkaido Univ., Sapporo, Japan Yurimoto. H. yuri@ep.sci.hokudai.ac.jp Dep. of Natural History Sciences, Hokkaido Univ., Sapporo, Japan Kakegawa, T. kakegawa@m.tohoku.ac.jp Dep. of Earth Science, Tohoku Univ., Sendai, Japan Geochemical data from ferruginous chemical sedimentary rocks (e.g., Banded Iron Formation: BIF) have been used to reconstruct the surface environments of early Earth. However, only a few studies have investigated the geochemical characteristics of BIFs deposited in a shallow water environment during the Archean, which may have differed from those deposited in a deep water environment. Therefore, we investigated geological, petrographic and geochemical characteristics of ferruginous rocks deposited in a shallow water environment in the Moodies group, in the Barberton Greenstone Belt, South Africa. We obtained ferruginous rock samples in the Moodies group from both an outcrop and underground gold mine, and compared the characteristics of these samples. The 70 sedimentary rock samples were divided into groups based on the dominant Fe minerals they contain: Hematite-rich jaspilite (HM group), Magnetite-rich iron formation/shale/sandstone (MT group), and Siderite-rich sandstone (SD group). Samples in the HM group are predominantly composed of fine-grained quartz (< 20 μm) and hematite (< 5 μm), which are interpreted to be chemical precipitates. Samples in the MT group contain quartz, magnetite, siderite, ankerite, chlorite, biotite and chromite. The grain size of magnetite is much larger (20-150 μm) than that of hematite in the HM group. The magnetite is interpreted as a secondary mineral transformed from hematite during early diagenesis. Results of in situ oxygen isotope analysis by SIMS showed that magnetite in the Moodies group has similar δ18O values to those in the least metamorphosed BIFs. All chromite observed in the MT group is overgrown by magnetite. Samples in the SD group contain quartz, siderite, chlorite, biotite, and chromite; the chromite is included in Mg-rich siderite or silicate minerals (e.g., chlorite and biotite). Oxygen isotope compositions indicate that chromite in both the MT and SD groups, was hydrothermally altered. Results of geochemical analyses of the bulk outcrop samples showed that FeTotal/Ti and Cr/Ti ratios of outcrop samples increase concordantly in the ferruginous zone, particularly in the MT group. The Cr/Ti ratios of the underground samples also increase with increasing the Fetotal/Ti ratios. On the other hand, Th/U ratios of both the outcrop and underground samples decrease with increasing FeTotal/Ti ratios. The correlations of Fetotal/Ti ratios with U/Th and Cr/Ti ratios indicate that dissolved Cr and U species in the ocean were coprecipitated with ferric (hydr)oxides during the formation of ferruginous rocks of the Moodies Group. These results suggest that Cr and U were chemically mobile, possibly as oxidized species, in the Earth's surface environment at ~3.2 Ga.

MINERALOGY, PETROGRAPHY, AND RADIOACTIVITY OF REPRESENTATIVE SAMPLES OF CHATTANOOGA SHALE

DOE Office of Scientific and Technical Information (OSTI.GOV)

Bates, T.F.; Strahl, E.O.

1957-01-01

Qualitative and quantitative mineralogical studies of the Chattanooga Shale are in progress. Problems of separation and analysis of mineral and organic components are difficult because the rock is fine-grained. However, the applicaiion of light and electron microscopy, x-ray diffraction, nuclear-track study, and other methods has provided data of interest. Megascopically, the shalc is a massive chocolate-brown sediment which displays faint indications of lamination. Some pyrite lenses, nodules, and crystals and a few mica flakes are large enough to be seen with a hand lens. In thin section the rock is seen to consist of grains of quartz and feldspar inmore » a matrix of yellow to red--brown organic material, which incorporates shreds of mica and probably clay particles and is dotted by small clusters of pyrite. Larger organic fragments with associated pyrite are common and take various forms. Individual mineral particles range from pyrite cubes less than 0.15 micron on a side to quartz and feldspar grains as large as 0.10 mm. X-ray studies show the clay minerals to be illite, kaolinite, and chlorite in decreasing order of abundance. Tourmaline, zircon, and apatite are the characteristic heavy minerals of the sediment. Quantitative studies, accomplished by a combination of chemical and mineralogical methods, have shown the composition of a batch sample of this rock to be approxiinately: 22% quartz, 9% feldspar, 31% illite and kaolinite, 22% organic matter, 11% pyrite and marcasite, 2% chlorite, 2% iron oxides, and l% tourmaline, zircon, and apatite. Alphatrack studies of cniulsion-covered thin sections indicate that no uranium mineral is present. Approximately 70% of the uranium atoms is randomly distributed throughout the finegrained matrix of the rock, whereas another 25% is concentrated in organic-pyrite-clay complexes such as pyrite nodules and discrete organic bodies. In unweathered samples there is no relationship between uranium distribution and textural fcatures such as bedding. The data indicate that the uranium was precipitated from sea water under reducing conditions and has not been redistributed following compaction of the sediment. (auth)« less

Structures, microfabrics and textures of the Cordilleran-type Rechnitz metamorphic core complex, Eastern Alps☆

PubMed Central

Cao, Shuyun; Neubauer, Franz; Bernroider, Manfred; Liu, Junlai; Genser, Johann

2013-01-01

Rechnitz window group represents a Cordilleran-style metamorphic core complex, which is almost entirely located within nearly contemporaneous Neogene sediments at the transition zone between the Eastern Alps and the Neogene Pannonian basin. Two tectonic units are distinguished within the Rechnitz metamorphic core complex (RMCC): (1) a lower unit mainly composed of Mesozoic metasediments, and (2) an upper unit mainly composed of ophiolite remnants. Both units are metamorphosed within greenschist facies conditions during earliest Miocene followed by exhumation and cooling. The internal structure of the RMCC is characterized by the following succession of structure-forming events: (1) blueschist relics of Paleocene/Eocene age formed as a result of subduction (D1), (2) ductile nappe stacking (D2) of an ophiolite nappe over a distant passive margin succession (ca. E–W to WNW–ESE oriented stretching lineation), (3) greenschist facies-grade metamorphism annealing dominant in the lower unit, and (4) ductile low-angle normal faulting (D3) (with mainly NE–SW oriented stretching lineation), and (5) ca. E to NE-vergent folding (D4). The microfabrics are related to mostly ductile nappe stacking to ductile low-angle normal faulting. Paleopiezometry in conjunction with P–T estimates yield high strain rates of 10− 11 to 10− 13 s− 1, depending on the temperature (400–350 °C) and choice of piezometer and flow law calibration. Progressive microstructures and texture analysis indicate an overprint of the high-temperature fabrics (D2) by the low-temperature deformation (D3). Phengitic mica from the Paleocene/Eocene high-pressure metamorphism remained stable during D2 ductile deformation as well as preserved within late stages of final sub-greenschist facies shearing. Chlorite geothermometry yields two temperature groups, 376–328 °C, and 306–132 °C. Chlorite is seemingly accessible to late-stage resetting. The RMCC underwent an earlier large-scale coaxial deformation accommodated by a late non-coaxial shear with ductile low-angle normal faulting, resulting in subvertical thinning in the extensional deformation regime. The RMCC was rapidly exhumed during ca. 23–18 Ma. PMID:27065502

Identification of mineral composition and weathering product of tuff using reflectance spectroscopy

NASA Astrophysics Data System (ADS)

Hyun, C.; Park, H.

2009-12-01

Tuff is intricately composed of various types of rock blocks and ash matrixes during volcanic formation processes. Qualitative identification and quantitative assessment of mineral composition of tuff usually have been done using manual inspection with naked-eyes and various chemical analyses. Those conventional methods are destructive to objects, time consuming and sometimes carry out biased results from subjective decision making. To overcome limits from conventional methods, assessment technique using reflectance spectroscopy was applied to tuff specimens. Reflectance spectroscopy measures electromagnetic reflectance on rock surface and can extract diagnostic absorption features originated from chemical composition and crystal structure of constituents in the reflectance curve so mineral species can be discriminated qualitatively. The intrinsic absorption feature from particular mineral can be converted to absorption depth representing relative coverage of the mineral in the measurement area by removing delineated convex hull from raw reflectance curve. The spectral measurements were performed with field spectrometer FieldSpec®3 of ASD Inc. and the wavelength range of measurement was form 350nm to 2500nm. Three types of tuff blocks, ash tuff, green lapilli tuff and red lapilli tuff, were sampled from Hwasun County in Korea and the types of tuffs. The differences between green tuff and red tuff are from the color of their matrixes. Ash tuff consists of feldspars and quartz and small amount of chalcedony, calcite, dolomite, epidote and basalt fragments. Green lapilli tuff consists of feldspar, quartz and muscovite and small amount of calcite, chalcedony, sericite, chlorite, quartzite and basalt fragments. Red lapilli tuff consists of feldspar, quartz and muscovite and small amount of calcite, chalcedony, limonite, zircon, chlorite, quartzite and basalt fragments. The tuff rocks were coarsely crushed and blocks and matrixes were separated to measure standard spectral reflectance of each constituent. Unmixing of mineral composition and their weathering products of blocks and matrixes in tuff were conducted and the ratio of mineral composition was calculated for each specimen. This study was supported by National Research Institute of Cultural Heritage (project title: Development on Evaluation Technology for Weathering Degree of Stone Cultural Properties, project no.: 09B011Y-00150-2009).

Determination of Geochemical Bio-Signatures in Mars-Like Basaltic Environments

PubMed Central

Olsson-Francis, Karen; Pearson, Victoria K.; Steer, Elisabeth D.; Schwenzer, Susanne P.

2017-01-01

Bio-signatures play a central role in determining whether life existed on early Mars. Using a terrestrial basalt as a compositional analog for the martian surface, we applied a combination of experimental microbiology and thermochemical modeling techniques to identify potential geochemical bio-signatures for life on early Mars. Laboratory experiments were used to determine the short-term effects of biota on the dissolution of terrestrial basalt, and the formation of secondary alteration minerals. The chemoorganoheterotrophic bacterium, Burkholderia sp. strain B_33, was grown in a minimal growth medium with and without terrestrial basalt as the sole nutrient source. No growth was detected in the absence of the basalt. In the presence of basalt, during exponential growth, the pH decreased rapidly from pH 7.0 to 3.6 and then gradually increased to a steady-state of equilibrium of between 6.8 and 7.1. Microbial growth coincided with an increase in key elements in the growth medium (Si, K, Ca, Mg, and Fe). Experimental results were compared with theoretical thermochemical modeling to predict growth of secondary alteration minerals, which can be used as bio-signatures, over a geological timescale. We thermochemically modeled the dissolution of the basalt (in the absence of biota) in very dilute brine at 25°C, 1 bar; the pH was buffered by the mineral dissolution and precipitation reactions. Preliminary results suggested that at the water to rock ratio of 1 × 107, zeolite, hematite, chlorite, kaolinite, and apatite formed abiotically. The biotic weathering processes were modeled by varying the pH conditions within the model to adjust for biologic influence. The results suggested that, for a basaltic system, the microbially-mediated dissolution of basalt would result in “simpler” secondary alteration, consisting of Fe-hydroxide and kaolinite, under conditions where the abiotic system would also form chlorite. The results from this study demonstrate that, by using laboratory-based experiments and thermochemical modeling, it is possible to identify secondary alteration minerals that could potentially be used to distinguish between abiotic and biotic weathering processes on early Mars. This work will contribute to the interpretation of data from past, present, and future life detection missions to Mars. PMID:28943863

Combining Textural Techniques to Explore Effects of Diagenesis and Low-grade Metamorphism on Iron Mineralogy and Iron Speciation

NASA Astrophysics Data System (ADS)

Slotznick, S. P.; Webb, S.; Eiler, J. M.; Kirschvink, J. L.; Fischer, W. W.

2016-12-01

Iron chemistry and mineralogy in the sedimentary rocks provide a valuable tool for studying paleoenvironmental conditions due to the fact that iron atoms can take on either the +II or +III valence state under geological redox conditions. One method utilizing this redox chemistry is `iron speciation', a bulk chemical sequential extraction technique that maps proportions of iron species to redox conditions empirically calibrated from modern sediments. However, all Precambrian and many Phanerozoic rocks have experienced post-depositional processes; it is vital to explore their effects on iron mineralogy and speciation. We combined light and electron microscopy, magnetic microscopy, (synchrotron-based) microprobe x-ray spectroscopy, and rock magnetic measurements in order to deconvolve secondary overprints from primary phases and provide quantitative measurement of iron minerals. These techniques were applied to excellently-preserved shale and siltstone samples of the 1.4 Ga lower Belt Supergroup, Montana and Idaho, USA, spanning a metamorphic gradient from sub-biotite to garnet zone. Previously measured Silurian-Devonian shales, sandstones, and carbonates in Maine and Vermont, USA spanning from the chlorite to kyanite zone provided additional well-constrained, quantitative data for comparison and to extend our analysis. In all of the studied samples, pyrrhotite formation occurred at the sub-biotite or sub-chlorite zone. Pyrrhotite was interpreted to form from pyrite and/or other iron phases based on lithology; these reactions can affect the paleoredox proxy. Iron carbonates can also severely influence iron speciation results since they often form in anoxic pore fluids during diagenesis; textural analyses of the Belt Supergroup samples highlighted that iron-bearing carbonates were early diagenetic cements or later diagenetic overprints. The inclusion of iron from diagenetic minerals during iron speciation analyses will skew results by providing a view of pore-fluid redox, not ancient water column chemistry. While our analyses and biological indicators suggest that the studied samples of the lower Belt Supergroup and New England were deposited in oxic water columns, iron speciation results imply anoxic/ferruginous conditions due to diagenetic alterations affecting the record.

Determination of Geochemical Bio-Signatures in Mars-Like Basaltic Environments.

PubMed

Olsson-Francis, Karen; Pearson, Victoria K; Steer, Elisabeth D; Schwenzer, Susanne P

2017-01-01

Bio-signatures play a central role in determining whether life existed on early Mars. Using a terrestrial basalt as a compositional analog for the martian surface, we applied a combination of experimental microbiology and thermochemical modeling techniques to identify potential geochemical bio-signatures for life on early Mars. Laboratory experiments were used to determine the short-term effects of biota on the dissolution of terrestrial basalt, and the formation of secondary alteration minerals. The chemoorganoheterotrophic bacterium, Burkholderia sp. strain B_33, was grown in a minimal growth medium with and without terrestrial basalt as the sole nutrient source. No growth was detected in the absence of the basalt. In the presence of basalt, during exponential growth, the pH decreased rapidly from pH 7.0 to 3.6 and then gradually increased to a steady-state of equilibrium of between 6.8 and 7.1. Microbial growth coincided with an increase in key elements in the growth medium (Si, K, Ca, Mg, and Fe). Experimental results were compared with theoretical thermochemical modeling to predict growth of secondary alteration minerals, which can be used as bio-signatures, over a geological timescale. We thermochemically modeled the dissolution of the basalt (in the absence of biota) in very dilute brine at 25°C, 1 bar; the pH was buffered by the mineral dissolution and precipitation reactions. Preliminary results suggested that at the water to rock ratio of 1 × 10 7 , zeolite, hematite, chlorite, kaolinite, and apatite formed abiotically. The biotic weathering processes were modeled by varying the pH conditions within the model to adjust for biologic influence. The results suggested that, for a basaltic system, the microbially-mediated dissolution of basalt would result in "simpler" secondary alteration, consisting of Fe-hydroxide and kaolinite, under conditions where the abiotic system would also form chlorite. The results from this study demonstrate that, by using laboratory-based experiments and thermochemical modeling, it is possible to identify secondary alteration minerals that could potentially be used to distinguish between abiotic and biotic weathering processes on early Mars. This work will contribute to the interpretation of data from past, present, and future life detection missions to Mars.

Provenance and composition of unusually chrome and nickel-rich bucket-shaped pottery from Rogaland (southwestern Norway)

NASA Astrophysics Data System (ADS)

Zimmermann, Udo; Kristoffersen, Elna Siv; Fredriksen, Per Ditlef; Bertolino, Silvana A. R.; Andò, Sergio; Bersani, Danilo

2016-05-01

We report results from FE-SEM-EDS, geochemical, mineralogical analyses and Raman spectroscopy of pottery of bucket-shaped ceramic from Rogaland (southwestern Norway) dated between the 5th and 6th Century. The study reveals a very rare pottery composition including asbestos-group minerals and an unusual enrichment in compatible elements like Cr (8-27 × Post Archean average shale (PAS), McLennan et al., 2006), Ni (2-8 × normal shale) and Co (2-3 × PAS). X-Rray diffraction and Raman spectroscopy could pinpoint that Ni is introduced by specific Ni-rich talc mineral and chlorite minerals and Cr occurs in a rare Cr-rich talc, and possibly in a Cr-chlorite, these minerals are the most abundant in the pottery, which is supported by strong enrichment in Mg (10-20 × PAS). The addition of Mg, Cr, Ni and Co and other compatible trace elements is to our current knowledge not caused by anthropogenic activity but related to the used materials, which are alteration products of mafic and ultramafic rocks or genetically related to mafic and ultramafic rocks. Rocks of this type are exposed in vicinity of the sampling areas in a region called Karmøy, hosting a world famous ophiolite complex, which is identified as the major source for the mafic and ultramafic component, as the next succession of a similar composition is far further north located in Norway and a number of rock types on Karmøy matches the chemical composition of the pottery. The here reported composition is spectacular and extremely rare - if ever found - in pottery. Our study shows that unusual material sources have been used in pottery production, and this opens for discussion whether the materials were deliberately selected by the manufacturers, thereby expressing a specific social function, in a time period where more functional clay types and additives, and certainly functional and sufficient for use in pottery, where abundant in areas of Rogaland closer to where the pots were found.

Slab melting and magma formation beneath the southern Cascade arc

USGS Publications Warehouse

Walowski, Kristina J.; Wallace, Paul J.; Clynne, Michael A.; Rasmussen, D.J.; Weis, D.

2016-01-01

The processes that drive magma formation beneath the Cascade arc and other warm-slab subduction zones have been debated because young oceanic crust is predicted to largely dehydrate beneath the forearc during subduction. In addition, geochemical variability along strike in the Cascades has led to contrasting interpretations about the role of volatiles in magma generation. Here, we focus on the Lassen segment of the Cascade arc, where previous work has demonstrated across-arc geochemical variations related to subduction enrichment, and H-isotope data suggest that H2O in basaltic magmas is derived from the final breakdown of chlorite in the mantle portion of the slab. We use naturally glassy, olivine-hosted melt inclusions (MI) from the tephra deposits of eight primitive (MgO>7 wt%) basaltic cinder cones to quantify the pre-eruptive volatile contents of mantle-derived melts in this region. The melt inclusions have B concentrations and isotope ratios that are similar to mid-ocean ridge basalt (MORB), suggesting extensive dehydration of the downgoing plate prior to reaching sub-arc depths and little input of slab-derived B into the mantle wedge. However, correlations of volatile and trace element ratios (H2O/Ce, Cl/Nb, Sr/Nd) in the melt inclusions demonstrate that geochemical variability is the result of variable addition of a hydrous subduction component to the mantle wedge. Furthermore, correlations between subduction component tracers and radiogenic isotope ratios show that the subduction component has less radiogenic Sr and Pb than the Lassen sub-arc mantle, which can be explained by melting of subducted Gorda MORB beneath the arc. Agreement between pMELTS melting models and melt inclusion volatile, major, and trace element data suggests that hydrous slab melt addition to the mantle wedge can produce the range in primitive compositions erupted in the Lassen region. Our results provide further evidence that chlorite-derived fluids from the mantle portion of the slab (∼7–9 km below the slab top) cause flux melting of the subducted oceanic crust, producing hydrous slab melts that migrate into the overlying mantle, where they react with peridotite to induce further melting.

Geochemical and tectonic implications on plate-interface evolution achieved from high-pressure ultramafic rocks in mélange settings

NASA Astrophysics Data System (ADS)

Cannaò, E.; Agostini, S.; Scambelluri, M.; Tonarini, S.

2014-12-01

Geochemical studies of fluid-mobile elements (FME) joined with B, Sr and Pb isotopic analyses of high-pressure mélanges terranes help constraining tectonic processes and mass transfer during accretion of slab and suprasubduction mantle in plate-interface domains. Here we focus on ultramafic rocks from two plate interface settings: (I) metasediment-dominated mélange (Cima di Gagnone, CdG, Adula Unit), where eclogite-facies de-serpentinized garnet peridotite and chlorite harzburgite lenses are embedded in paraschist; (II) dominated by high-pressure serpentinite (Erro-Tobbio, ET, and Voltri Units, VU, Ligurian Alps). CdG metaperidotite shows low [B], negative δ 11B and high Sr and Pb isotopic ratios. As, Sb loss from metasediment and gain by garnet and chlorite metaperidotite points to exchange between the two systems. Presence of As and Sb in eclogite-facies peridotite minerals and preferential low-T mobility of such elements suggest that exchange was during early subduction burial and prior to eclogitization. Based on high [B], positive δ11B, oxygen and hydrogen isotope, the ET serpentinties were recently interpreted as supra-subduction mantle flushed by slab fluids (Scambelluri & Tonarini, 2012, Geology, 40, 907-910). Their 206Pb/204Pb and 87Sr/86Sr isotope ratios range between 18.300-18.514 and 0.7048-0.7060, respectively. Compared with ET rocks, VU serpentinites have higher As, Sb (up to 1.3 and 0.39 ppm, respectively) and are enriched in radiogenic Sr (up to 0.7105 87Sr/86Sr). This signature reflects interaction with fluids that exchanged with sedimentary rocks, either in outer rise environments or during accretion atop the slab. In the above cases, the serpentinized mantle rocks fingerprint interaction with fluids from different sources, indicating a timing of accretion to plate interface domains. We provide evidence that serpentinized mantle slices of different size and provenance (slab or wedge) accreted to plate interface domains since early subduction stages. They also represent FME and radiogenic isotope sources for arcs and for deep mantle refertilization.

Petrogenesis of cataclastic rocks within the San Andreas fault zone of Southern California U.S.A.

NASA Astrophysics Data System (ADS)

Lawford Anderson, J.; Osborne, Robert H.; Palmer, Donald F.

1980-08-01

This paper petrologically characterizes cataclastic rocks derived from four sites within the San Andreas fault zone of southern California. In this area, the fault traverses an extensive plutonic and metamorphic terrane and the principal cataclastic rock formed at these upper crustal levels is unindurated gouge derived from a range of crystalline rocks including diorite, tonalite, granite, aplite, and pegmatite. The mineralogical nature of this gouge is decidedly different from the "clay gouge" reported by Wu (1975) for central California and is essentially a rock flour with a quartz, feldspar, biotite, chlorite, amphibole, epidote and oxide mineralogy representing the milled-down equivalent of the original rock. Clay development is minor (less than 4 wt. %) to nonexistent and is exclusively kaolinite. Alterations involve hematitic oxidation, chlorite alteration on biotite and amphibole, and local introduction of calcite. Electron microprobe analysis showed that in general the major minerals were not reequilibrated with the pressure—temperature regime imposed during cataclasis. Petrochemically, the form of cataclasis that we have investigated is largely an isochemical process. Some hydration occurs but the maximum amount is less than 2.2% added H 2O. Study of a 375 m deep core from a tonalite pluton adjacent to the fault showed that for Si, Al, Ti, Fe, Mg, Mn, K, Na, Li, Rb, and Ba, no leaching and/or enrichment occurred. Several samples experienced a depletion in Sr during cataclasis while lesser number had an enrichment of Ca (result of calcite veining). Texturally, the fault gouge is not dominated by clay-size material but consists largely of silt and fine sand-sized particles. An intriguing aspect of our work on the drill core is a general decrease in particulate size with depth (and confining pressure) with the predominate shifting sequentially from fine sand to silt-size material. The original fabric of these rocks is commonly not disrupted during the cataclasis. It is evident that the gouge development in these primarily igneous crystalline terranes is largely an in situ process with minimal mixing of rock types. Fabric analyses reveal that brecciation (shattering), not shearing, is the major deformational mechanism at these upper crustal levels.

Geologic setting, genesis and transformation of sulfide deposits in the northern part of Khetri copper belt, Rajasthan, India — an outline

NASA Astrophysics Data System (ADS)

Sarkar, S. C.; Dasgupta, Somnath

1980-07-01

The present study is confined to the northern part of the Khetri copper belt that extends for about 100 km in northern Rajasthan. Mineralization is more or less strata-bound and is confined to the garnetiferous chlorite schist and banded amphibolite quartzite, occurring towards the middle of the Proterozoic Delhi Supergroup. Preserved sedimentary features and re-estimation of the composition of the pre-metamorphic rocks suggest that the latter were deposited in shallow marine environment characterized by tidal activity. Cordierite-orthoamphibole-cummingtonite rock occurring in the neighbourhood of the ores is discussed, and is suggested to be isochemically metamorphosed sediment. The rocks together with the ores were deformed in two phases and metamorphosed in two progressive and one retrogressive events of metamorphism. Study of the host rocks suggests that the maximum temperature and pressure attained during metamorphism are respectively 550 600°C and < 5.5 kb. Principal ore minerals in Madan Kudan are chalcopyrite, pyrrhotite, pyrite and locally magnetite. In Kolihan these are chalcophyrite, pyrrhotite and cubanite. Subordinate phases are sphalerite, ilmenite, arsenopyrite, mackinawite, molybdenite, cobaltite and pentlandite. The last two are very rare. Gangue minerals comprise quartz, chlorite, garnet, amphiboles, biotite, scapolite, plagioclase and graphite. The ores are metamorphosed at temperatures > 491°C. Sulfide assemblages are explained in terms of fS 2 during metamorphism. Co-folding of the ore zone with the host rocks, confinement of the ores to the carbonaceous pelites or semi-pelitic rocks, strata-bound and locally even stratiform nature of the orebodies, lack of finite ‘wall rock alteration’, metamorphism of the ores in the thermal range similar to that for the host rocks, absence of spatial and temporal relationship with the granitic rocks of the region led the authors to conclude that the entire mineralization was originally sedimentary-diagenetic. Any loss of primitive features and development of incongruency are due to subsequent deformation and metamorphism to which the ores and their hosts were together subjected.

Decreased dosage of acidified sodium chlorite reduces microbial contamination and maintains organoleptic qualities of ground beef products.

PubMed

Bosilevac, Joseph M; Shackelford, Steven D; Fahle, Rick; Biela, Timothy; Koohmaraie, Mohammad

2004-10-01

Acidified sodium chlorite (ASC) spray was evaluated at decreased dosages and application rates to determine its efficacy for reducing bacterial contamination on boneless beef trimmings used for production of raw ground beef products while maintaining desirable consumer qualities in the finished ground beef products. Two different applications of ASC (600 ppm applied at a rate of 1.3 oz/lb and 300 ppm applied at a rate of 1 oz/lb) were used to treat boneless beef trimmings before grinding. The effect of ASC treatment on 50/50 lean beef trimmings was greater than on 90/10 trimmings. ASC at 600 ppm reduced both the aerobic plate counts (APC) and Enterobacteriaceae counts (EBC) by 2.3 log CFU/g on 50/50 trimmings, whereas treatment with 300 ppm ASC reduced APC and EBC of 50/50 trimmings by 1.1 and 0.7 log CFU/g, respectively. Ground beef formulations of 90/10 and 73/27 were produced from the treated boneless beef trim and packaged in chubs and in modified atmosphere packaging. The efficacy of ASC spray treatment to inhibit APC and EBC over the shelf life of each ground beef product was monitored. The APC and EBC in ground beef chubs were reduced by 1.0 to 1.5 log CFU/g until day 20. The APC and EBC for products in modified atmosphere packaging were reduced 1.5 to 3.0 log CFU/g throughout their shelf life. Both decreased dosages of ASC were equally effective on 90/10 lean ground beef, but the 300 ppm ASC treatment was slightly better at reducing the EBC of 73/27 ground beef. The organoleptic qualities (color, odor, and taste) of the ground beef products treated with 300 ppm ASC were found to be superior to those treated with 600 ppm ASC. Our results indicated that decreased dosages of ASC reduce contamination and lengthen the shelf life of ground beef. Furthermore, the 300 ppm ASC treatment reduced bacterial counts while maintaining desirable organoleptic ground beef qualities.

Origin of CaCl2 brines by basalt-seawater interaction: Insights provided by some simple mass balance calculations

NASA Astrophysics Data System (ADS)

Hardie, Lawrence A.

1983-06-01

Modern rift zone hydrothermal brines are typically CaCl2-bearing brines, an unusual chemical signature they share with certain oil field brines, fluid inclusions in ore minerals and a few uncommon saline lakes. Many origins have been suggested for such CaCl2 brines but in the Reykjanes, Iceland, geothermal system a strong empirical case can be made for a basalt-seawater interaction origin. To examine this mechanism of CaCl2 brine evolution some simple mass balance calculations were carried out. Average Reykjanes olivine tholeiite was “reacted” with average North Atlantic seawater to make an albite-chlorite-epidotesphene rock using Al2O3 as the conservative rock component and Cl as the conservative fluid component. The excess components released by the basalt to the fluid were “precipitated” at 275° C as quartz, calcite, anhydrite, magnetite and pyrite to complete the conversion to greenstone. The resulting fluid was a CaCl2 brine of seawater chlorinity with a composition remarkably similar to the actual Reykjanes brine at 1750 m depth. Thus, the calculations strongly support the idea that the Reykjanes CaCl2 brines result from “closed system” oceanic basalt-seawater interaction (albitization — chloritization mechanism) at greenschist facies temperatures. The calculation gives a seawater: basalt mass ratio of 3∶1 to 4∶1 (vol. ratio of 9∶1 to 12∶1), in keeping with experimental results, submarine vent data and with ocean crust cooling calculations. The brine becomes anoxic because there is insufficient dissolved or combined oxygen to balance all the Fe released from the basalt during alteration. Large excesses of Ca are released to the fluid and precipitate out in the form of anhydrite which essentially sweeps the brine free of sulfate leaving an elevated Ca concentration. The calculated rock-water interaction basically involves Na + Mg + SO4 ⇌ Ca + K, simulating chemical differences observed between oceanic basalts and greenstones from many mid-ocean ridges.

Textures and compositions of cobalt pentlandite and cobaltian mackinawite from the Madan-Kudan copper deposit, Khetri Copper Belt, Rajasthan, India

NASA Astrophysics Data System (ADS)

Baidya, Abu Saeed; Sen, Atlanta; Pal, Dipak C.

2018-06-01

The Khetri Copper Belt (KCB), a part of the Proterozoic Delhi-Aravalli fold belt in western India, hosts several Cu deposits, which are known to contain considerable Au, Ag, Co and Ni. Although many Co-bearing phases have been reported from the KCB and adjacent areas, detailed textural and geochemical data are either unavailable or scant except for mackinawite. In this study, we describe the textures and compositions (determined by EPMA) of two very rare Co-rich phases, namely cobaltian mackinawite (containing up to 12.68 wt.% Co, 1.90 wt.% Ni and 2.52 wt.% Cu) and cobalt-pentlandite (containing up to 49.30 wt.% Co and 10.19 wt.% Ni), identified based on composition, from the Madan-Kudan deposit. To the best of our knowledge, neither cobalt-pentlandite nor such highly Co-rich mackinawite have previously been reported from this area. The common sulphide minerals viz. chalcopyrite, pyrrhotite and rare pyrite occur in chalcopyrite-pyrrhotite ± pyrite-magnetite-chlorite-blue amphibole (Cl-rich hastingsite-pargasite-sadanagaite) ± marialitic scapolite ± allanite ± uraninite veins in amphibole-bearing feldspathic quartzite and garnetiferous chlorite schist. Cobaltian mackinawite is invariably associated with chalcopyrite and occurs as exsolution and inclusion within chalcopyrite or outside, but at the contact of chalcopyrite. On the other hand, cobalt-pentlandite is invariably associated with pyrrhotite and shows similar textural relation with pyrrhotite as that of mackinawite with chalcopyrite. Mineralogically diverse undeformed sulphide veins comprising Cl-rich amphibole and locally Cl-rich marialitic scapolite suggests epigenetic hydrothermal mineralization involving Cl-rich saline fluid in the Madan-Kudan deposit. Transport of metals, derived from a mafic source rock with high intrinsic Ni:Co ratio, by Cl-rich fluid can suitably explain the high Co:Ni ratio of the studied ore minerals. Presence of such highly Co-rich phases and other circumstantial evidences, enumerated in this work, are consistent with variants of Fe oxide (-Cu-Au) (IOCG) style mineralization, at least for some stages of mineralization in the Madan-Kudan deposit.

Constraining the thermal structure beneath Lusi: insights from temperature record in erupted clasts

NASA Astrophysics Data System (ADS)

Malvoisin, Benjamin; Mazzini, Adriano; Miller, Stephen

2016-04-01

Sedimentary units beneath Lusi from surface to depth are the Pucangan formation, the Upper Kalibeng formation where shales and then volcanoclastic clasts are found, the Kujung-Propuh-Tuban formation composed of carbonates and the Ngimbang formation composed of shales. Water and gas geochemistry as well as surface deformation indicate that Lusi is a hydrothermal system rooted at >4 km depth. However, the thermal structure beneath Lusi is still poorly constrained whereas it has first-order impacts on the physical and chemical processes observed during the eruption. In the framework of the Lusi Lab project (ERC grant n° 308126) and of a project of the Swiss National Science Foundation (n°160050) we studied erupted clasts collected at the crater site to determine their source and temperature record. Three types of clasts were studied based on morphological and mineralogical basis. The first type is limestones mainly composed of Ca- and Fe-bearing carbonates. The clasts of the second type are light grey shales (LGS) containing carbonaceous matter, illite/smectite mixture, plagioclase and quartz. The third type is also a shale with a black colour containing hydrocarbons (black shales, BS) and with the additional presence of Na-rich plagioclase, biotite and chlorite. The presence of these latter minerals indicates hydrothermal activity at relatively high temperature. Better constraints on temperature were obtained by using both Raman spectroscopic carbonaceous material thermometry (RSCM) and chlorite geothermometry. Temperatures below 200°C were determined for the LGS with RSCM. BS recorded two temperatures. The first one, around 170°C, is rather consistent with an extrapolation of the geothermal gradient measured before the eruption up to 4,000 m depth. Combined with mineralogical observations, this suggests that BS originate from the Ngimbang formation. The second recorded higher temperature around 250°C indicates heating, probably through interaction with high temperature hydrothermal fluids. Calculations performed for such a heating indicate that associated clay dehydration is sufficient to provide the water released during the eruption and that heating-induced overpressure could favor fluid ascent. These results confirm the hydrothermal scenario in which Lusi eruption is fed by high temperature fluid circulation from the neighboring Arjuno-Welirang volcanic complex.

Long-term variations of clay mineral composition in the Andaman Sea (IODP Exp. 353 Site U1447): preliminary result

NASA Astrophysics Data System (ADS)

Lee, J.; Khim, B. K.; Cho, H. G.; Kim, S.; 353 Scientists, I. E.

2016-12-01

Clay mineral studies in the Bengal Fan have allowed the reconstruction of the erosional history of the Himalayan-Tibetan complex since the Early Miocene. Several factors such as climate change and tectonic activity are important for the erosion rate of the Himalaya-Tibet complex. IODP Expedition 353 Site U1447 (10°47.4'N, 93°00'E; 1391 mbsl) was drilled on a ridge 45 km offshore Little Andaman Island in the Andaman Sea, penetrating to total depths of 738 m. Riverine sediments supplied mainly by the Irrawaddy and Salween (draining the Indo-Burman Ranges; smectite-rich) and the Ganga/Brahmaputra (draining the Himalaya; illite-rich) via the surface currents have been known to deposit in the Andaman Sea. We measured clay minerals of 38 sediment samples collected from 150 to 737 m CSF-A at Site U1447 in order to reveal long-term variation patterns of clay minerals and their controlling factors. Age reconstruction of Site U1447 aided by shipboard biostratigraphic and paleomagnetic data defined the study interval spanning from the Late Miocene ( 10 Ma) to Early Pleistocene ( 1.25 Ma). At this interval, clay minerals consist mainly of smectite (28-61% with an average of 47%) followed by illite (20-41% with an average of 29%), kaolinite (9-19% with an average of 14%), and chlorite (5-15% with an average of 10%). Variation of clay mineral compositions is divided into three stages; almost consistent variations of all clay minerals (from 750 to 570 m CSF-A; 10.0 to 7.5 Ma), gradual decrease of smectite and increase of illite and chlorite (from 570 to 400 m CSF-A; 7.5 to 4.5 Ma), and great fluctuation of all clay minerals (from 400 to 150 m CSF-A; 4.5 to 1.1 Ma). Such long-term clay mineral changes may be related to provenance switches, tectonic evolution of the source regions, climatic variations, degree of volcanism with basin evolution, sedimentation history by sea level changes or some combination of these factors.

Fault-zone structure and weakening processes in basin-scale reverse faults: The Moonlight Fault Zone, South Island, New Zealand

NASA Astrophysics Data System (ADS)

Alder, S.; Smith, S. A. F.; Scott, J. M.

2016-10-01

The >200 km long Moonlight Fault Zone (MFZ) in southern New Zealand was an Oligocene basin-bounding normal fault zone that reactivated in the Miocene as a high-angle reverse fault (present dip angle 65°-75°). Regional exhumation in the last c. 5 Ma has resulted in deep exposures of the MFZ that present an opportunity to study the structure and deformation processes that were active in a basin-scale reverse fault at basement depths. Syn-rift sediments are preserved only as thin fault-bound slivers. The hanging wall and footwall of the MFZ are mainly greenschist facies quartzofeldspathic schists that have a steeply-dipping (55°-75°) foliation subparallel to the main fault trace. In more fissile lithologies (e.g. greyschists), hanging-wall deformation occurred by the development of foliation-parallel breccia layers up to a few centimetres thick. Greyschists in the footwall deformed mainly by folding and formation of tabular, foliation-parallel breccias up to 1 m wide. Where the hanging-wall contains more competent lithologies (e.g. greenschist facies metabasite) it is laced with networks of pseudotachylyte that formed parallel to the host rock foliation in a damage zone extending up to 500 m from the main fault trace. The fault core contains an up to 20 m thick sequence of breccias, cataclasites and foliated cataclasites preserving evidence for the progressive development of interconnected networks of (partly authigenic) chlorite and muscovite. Deformation in the fault core occurred by cataclasis of quartz and albite, frictional sliding of chlorite and muscovite grains, and dissolution-precipitation. Combined with published friction and permeability data, our observations suggest that: 1) host rock lithology and anisotropy were the primary controls on the structure of the MFZ at basement depths and 2) high-angle reverse slip was facilitated by the low frictional strength of fault core materials. Restriction of pseudotachylyte networks to the hanging-wall of the MFZ further suggests that the wide, phyllosilicate-rich fault core acted as an efficient hydrological barrier, resulting in a relatively hydrous footwall and fault core but a relatively dry hanging-wall.

Metaultramafic schists and dismembered ophiolites of the Ashe Metamorphic Suite of northwestern North Carolina, USA

USGS Publications Warehouse

Raymond, Loren A.; Merschat, Arthur J.; Vance, R. Kelly

2016-01-01

Metaultramafic rocks (MUR) in the Ashe Metamorphic Suite (AMS) of northwestern North Carolina include quartz ± feldspar-bearing QF-amphibolites and quartz-deficient, locally talc-, chlorite-, and/or Mg-amphibole-bearing TC-amphibolites. Some workers divide TC-amphibolites into Todd and Edmonds types, based on mineral and geochemical differences, and we provisionally add a third type – olivine ± pyroxene-rich, Rich Mountain-type rocks. Regionally, MUR bodies range from equant, Rich Mountain- to highly elongate, Todd-TC-amphibolite-type bodies. The MURs exhibit three to five mineral associations containing assemblages with olivine, anthophyllitic amphibole, Mg-hornblende, Mg-actinolite, cummingtonite, and serpentine representing decreasing eclogite to greenschist facies grades of metamorphism over time. MUR protoliths are difficult to determine. Southwestern MUR bodies have remnant olivine ± pyroxene-rich assemblages representing ultrabasic-basic, dunite-peridotite-pyroxenite protoliths. Northeastern TC-amphibolite MURs contain hornblende and actinolitic amphiboles plus chlorites – aluminous and calcic assemblages suggesting to some that metasomatism of basic, QF-amphibolites yields all TC-amphibolites. Yet MgO-CaO-Al2O3 and trace element chemistries of many TC-amphibolites resemble compositions of plagioclase peridotites. We show that a few AMS TC-amphibolites had basaltic/gabbroic protoliths, while presenting arguments opposing application of the metasomatic hypothesis to all TC-amphibolites. We establish that MUR bodies are petrologically heterolithic and that TC-amphibolites are in contact with many rock types; that those with high Cr, Ni, and Mg have olivine- or pyroxene-dominated protoliths; that most exhibit three or more metamorphic mineral associations; and that contacts thought to be metasomatic are structural. Clearly, different MUR bodies have different chemistries representing various protoliths, and have different mineral assemblages, reflecting both chemical composition and metamorphic history. Spot sampling of heterolithic MUR bodies does not reveal MUR body character or history or allow ‘type’ designations. We recommend that the subdivision of MUR bodies into ‘types’ be abandoned and that the metasomatic hypothesis be carefully applied. AMS MURs and associated metamafic rocks likely represent fragments of dismembered ophiolites from various ophiolite types.

Effects of chemical alteration on fracture mechanical properties in hydrothermal systems

NASA Astrophysics Data System (ADS)

Callahan, O. A.; Eichhubl, P.; Olson, J. E.

2015-12-01

Fault and fracture networks often control the distribution of fluids and heat in hydrothermal and epithermal systems, and in related geothermal and mineral resources. Additional chemical influences on conduit evolution are well documented, with dissolution and precipitation of mineral species potentially changing the permeability of fault-facture networks. Less well understood are the impacts of chemical alteration on the mechanical properties governing fracture growth and fracture network geometry. We use double-torsion (DT) load relaxation tests under ambient air conditions to measure the mode-I fracture toughness (KIC) and subcritical fracture growth index (SCI) of variably altered rock samples obtained from outcrop in Dixie Valley, NV. Samples from southern Dixie Valley include 1) weakly altered granite, characterized by minor sericite in plagioclase, albitization and vacuolization of feldspars, and incomplete replacement of biotite with chlorite, and 2) granite from an area of locally intense propylitic alteration with chlorite-calcite-hematite-epidote assemblages. We also evaluated samples of completely silicified gabbro obtained from the Dixie Comstock epithermal gold deposit. In the weakly altered granite KIC and SCI are 1.3 ±0.2 MPam1/2 (n=8) and 59 ±25 (n=29), respectively. In the propylitic assemblage KIC is reduced to 0.6 ±0.1 MPam1/2 (n=11), and the SCI increased to 75 ±36 (n = 33). In both cases, the altered materials have lower fracture toughness and higher SCI than is reported for common geomechanical standards such as Westerly Granite (KIC ~1.7 MPam1/2; SCI ~48). Preliminary analysis of the silicified gabbro shows a significant increase in fracture toughness, 3.6 ±0.4 MPam1/2 (n=2), and SCI, 102 ±45 (n=19), compared to published values for gabbro (2.9 MPam1/2 and SCI = 32). These results suggest that mineralogical and textural changes associated with different alteration assemblages may result in spatially variable rates of fracture initiation and growth in different parts of hydrothermal systems. Contrasting fracture mechanical properties between alteration assemblages may constitute a new mechanism of chemical-mechanical feedback that contributes to the localization of conduits in hydrothermal systems.

Chemical characterization of surface snow in Istanbul (NW Turkey) and their association with atmospheric circulations.

PubMed

Baysal, Asli; Baltaci, Hakki; Ozbek, Nil; Destanoglu, Orhan; Ustabasi, Gul Sirin; Gumus, Gulcin

2017-06-01

The understanding of the impurities in natural snow is important in realizing its atmospheric quality, soil characteristics, and the pollution caused to the environment. Knowledge of the occurrence of major ions and trace metals in the snow in the megacity of Istanbul is very limited. This manuscript attempts to understand the origin of major soluble ions (fluoride, acetate, formate, chlorite, chloride, nitrite, chlorate, bromide, nitrate, sulfate, phosphate, and perchlorate) and some trace metals (Fe, Mn, Cd, Co, Ni, Pb, Zn, Cu) in winter surface snow, collected in Istanbul, Turkey. The sampling of the surface snow was conducted after each precipitation during the winter of 2015-2016 at three sites in the city. Besides the statistical evaluation of the major ions, and some trace metal concentrations, the chemical variations along with atmospheric circulations, which are important modification mechanisms that influence the concentrations, were investigated in the study. At examined locations and times, 12 major anions were investigated and in these anions fluoride, chlorite, chlorate, bromide, and perchlorate in the snow samples were below the detection limit; only SO 4 2- , NO 3 - , and CI - were found to be in the range of 1.11-17.90, 0.75-4.52, and 0.19-3.01 mg/L. Also, according to the trace element determination, the concentration was found to be 29.2-53.7, 2.0-16.1, 1.0-2.2, 50.1-71.1, 24.2-35.2, ND-7.9, 43.2-106.6, and 3.0-17.7 μg/L for Fe, Mn, Cd, Co, Ni, Pb, Zn, and Cu, respectively. The major anions and investigated trace elements here originated mainly from anthropogenic and atmospheric circulation and mainly influenced by northerly and southerly circulation patterns. While the main limitations in the present study may be the low number of samples that may not be entirely representative, accurately reflect identification, or support other previously observed local measurements, we believe that the type of data presented in this study has the potential to be used in the field of environmental risk assessment and, as result, for human health.

Constraints on the timing of Marinoan ``Snowball Earth'' glaciation by 187Re-187Os dating of a Neoproterozoic, post-glacial black shale in Western Canada

NASA Astrophysics Data System (ADS)

Kendall, Brian S.; Creaser, Robert A.; Ross, Gerald M.; Selby, David

2004-06-01

New Re-Os isotopic data were obtained from chlorite-grade black shales from the upper Old Fort Point Formation (Windermere Supergroup), a post-glacial Neoproterozoic marker horizon in western Canada. A Re-Os isochron date of 634±57 Ma (MSWD=65, n=5) was determined using the conventional inverse aqua regia digestion medium. However, dissolution of the same samples with a new CrO 3-H 2SO 4 dissolution technique [Chem. Geol. 200 (2003) 225] yielded a much more precise date of 607.8±4.7 Ma (MSWD=1.2). Both dates are in agreement with existing U-Pb age constraints that bracket the Old Fort Point Formation between ˜685 and ˜570 Ma. The distinctive Re-Os systematics recorded by the two analytical protocols is explained by dissolution of a variably radiogenic, detrital Os component by the aqua regia method. In contrast, the CrO 3-H 2SO 4 technique minimizes this detrital component by selectively dissolving organic matter that is dominated by hydrogenous (seawater) Re and Os. The date of 607.8±4.7 Ma is thus interpreted as the depositional age for the upper Old Fort Point Formation providing a minimum age constraint for the timing of the second Windermere glaciation in western Canada. This ice age is correlative with the Marinoan (˜620-600 Ma) ice age and older than the ˜580-Ma Gaskiers glaciation of northeastern North America. The new Re-Os age determined from the CrO 3-H 2SO 4 digestion technique thus provides further support to a growing body of evidence for a global Marinoan glacial episode. Such an interpretation would not be discernable from the imprecise Re-Os date obtained with the aqua regia protocol. These results also indicate the potential for Re-Os radiometric dating of black shales that was not previously recognized. Importantly, neither chlorite-grade metamorphism nor the low organic content (TOC <1%) of the Old Fort Point Formation precluded the determination of a precise Re-Os depositional age using the CrO 3-H 2SO 4 analytical protocol.

Geochemistry, Metamorphic Assemblages, and Microstructures in Small Ultramafic Bodies from the Northern Nason Terrane, Washington

NASA Astrophysics Data System (ADS)

Magloughlin, J. F.

2014-12-01

Ultramafic bodies ranging from <1 to 2500 m in length occur in multiple settings across the northern part of the Nason Terrane in the North Cascade Mountains of Washington State. Within the Wenatchee Ridge Orthogneiss (WRO) the bodies are approximately equidimensional, ranging from dm-scale metasomatized lenses up to an exposed diameter of (typically) approximately 40 m. Some bodies are completely serpentinized, but others include dunite, harzburgite, and rare seams of pyroxenite. Many are rimmed by blackwall (talc, phlogopite, tremolite, chlorite, serpentine) coinciding with the Late Cretaceous metamorphism. The Napeequa Ultramafic Body (NUB), cut through and well exposed by the Napeequa River west of Lake Wenatchee, is within the White River Shear Zone (WRSZ, Magloughlin & McEwan, 1988). Though highly variable, it consists of dunite and peridotite and is variably serpentinized with common Mg-amphibole. Assemblages include serp+carb+chl+talc+opq and suggest upper greenschist to low amphibolite facies overprinting. Rare high-strain zones resemble relict pseudotachylyte veins. More common are ultramylonitic zones with olivine grain sizes of <5 microns, suggesting terrane-boundary paleostresses of >250 MPa. The Nine Mile Creek Ultramafic Body (NMCUB) and Grave Ultramafic Body (GUB) are the largest bodies outside of the White River Shear Zone, and are approximately 300 m and 800 long, respectively. Both are characterized by ol+talc+amph along with chlorite pseudomorphs, commonly cut by <40 micron thick ribbons of calcite, and rarely containing Si defined by chromite. These tectonites contain fine-grained olivine, but post-deformational, metamorphic cummingtonite and tremolite. In both bodies, a moderate to strong foliation is developed. It is suggested both bodies are retrogressed garnet peridotites. An interesting problem is why the possible retrogressed garnet peridotite bodies are present south of the WRSZ and surrounded by the metatonalites of the WRO, but none are present within the WRSZ. The extreme variability of the ultramafic bodies south of the WRSZ, and their presence within the WRO pluton, suggests a possible stoping mechanism from a heterogeneous ultramafic-rich sole of the WRSZ, or a possibly now-eroded splay of that shear zone.

Implications of spinel compositions for the petrotectonic history of abyssal peridotite from Southwest Indian Ridge (SWIR)

NASA Astrophysics Data System (ADS)

Chen, T.; Jin, Z.; Wang, Y.; Tao, C.

2012-12-01

Abyssal peridotites generate at mid-ocean ridges. Lherzolite and harzburgite are the main rock types of peridotites in the uppermost mantle. The lherzolite subtype, less depleted and less common in ophiolites, characterizes mantle diapirs and slow-spreading ridges. Along the Earth's mid-ocean ridges, abyssal peridotites undergo hydration reactions to become serpentinite minerals, especially in slow to ultraslow spreading mid-ocean ridges. Spinel is common in small quantities in peridotites, and its compositions have often been used as petrogenetic indicators [1]. The Southwest Indian Ridge (SWIR) is one of the two ultraslow spreading ridges in the world. The studied serpentinized peridotite sample was collected by the 21st Voyage of the Chinese oceanic research ship Dayang Yihao (aka Ocean No. 1) from a hydrothermal field (63.5°E, 28.0°S, and 3660 m deep) in SWIR. The studied spinels in serpentinized lherzolite have four zones with different compositions: relic, unaltered core is magmatic Al-spinels; micro- to nano- sized ferrichromite zoned particles; narrow and discontinuous magnetite rim; and chlorite aureoles. The values Cr# of the primary Al-spinels indicate the range of melting for abyssal peridotites from SWIR extends from ~4% to ~7% [2]. The alteration rims of ferrichromite have a chemical composition characterized by Fe enrichment and Cr# increase indicating chromite altered under greenschist-amphibolite facies. Magnetites formed in syn- and post- serpentinization. Chlorite (clinochlore) formed at the boundary and crack of spinel indicating it had undergone with low-temperature MgO- and SiO2-rich hydrothermal fluids [3]. It suggests that serpentinized lherzolite from SWIR had undergone poly-stage hydration reactions with a wide range of temperature. Acknowledgments: EMPA experiment was carried out by Xihao Zhu and Shu Zheng in The Second Institute of Oceanography and China University of Geosciences, respectively. The work was supported by NSFC. References [1] Dick, H.J.B., et al., Contrib Mineral Petr., 86:54, 1984. [2] Hellebrand et al., Nature, 410: 677, 2001. [3] Hamdy, M.M. , et al., JGMR, 3(9): 232, 2011.

Evidence of negative-index refraction in nonlinear chemical waves.

PubMed

Yuan, Xujin; Wang, Hongli; Ouyang, Qi

2011-05-06

The negative index of refraction of nonlinear chemical waves has become a recent focus in nonlinear dynamics researches. Theoretical analysis and computer simulations have predicted that the negative index of refraction can occur on the interface between antiwaves and normal waves in a reaction-diffusion (RD) system. However, no experimental evidence has been found so far. In this Letter, we report our experimental design in searching for such a phenomenon in a chlorite-iodide-malonic acid (CIMA) reaction. Our experimental results demonstrate that competition between waves and antiwaves at their interface determines the fate of the wave interaction. The negative index of refraction was only observed when the oscillation frequency of a normal wave is significantly smaller than that of the antiwave. All experimental results were supported by simulations using the Lengyel-Epstein RD model which describes the CIMA reaction-diffusion system.

Evaluating the effect of spatial subsetting on subpixel unmixing methodology applied to ASTER over a hydrothermally altered terrain

NASA Astrophysics Data System (ADS)

Ayoobi, Iman; Tangestani, Majid H.

2017-10-01

This study investigates the effect of spatial subsets of Advanced Spaceborne Thermal Emission and Reflection radiometer (ASTER) L1B visible-near infrared and short wave-infrared (VNIR-SWIR) data on matched filtering results at the central part of Kerman magmatic arc, where abundant porphyry copper deposits exist. The matched filtering (MF) procedure was run separately at sites containing hydrothermal minerals such as sericite, kaolinite, chlorite, and jarosite to map the abundances of these minerals on spatial subsets containing 100, 75, 50, and 25 percent of the original scene. Results were evaluated by comparing the matched filtering scores with the mineral abundances obtained by semi-quantitative XRD analysis of corresponding field samples. It was concluded that MF method should be applied to the whole scene prior to any data subsetting.

Partial structural characterization and antioxidant activity of a phenolic-xylan from Castanea sativa hardwood.

PubMed

Renault, Emmanuel; Barbat-Rogeon, Aline; Chaleix, Vincent; Calliste, Claude-Alain; Colas, Cyril; Gloaguen, Vincent

2014-09-01

4-O-Methylglucuronoxylans (MGX) were isolated from chestnut wood sawdust using two different procedures: chlorite delignification followed by the classical alkaline extraction step, and an unusual green chemistry process of delignification using phthalocyanine/H2O2 followed by a simple extraction with hot water. Antioxidant properties of both MGX were evaluated against the stable radical 2,2-diphenyl-1-picrylhydrazyl (DPPH) by electronic spin resonance (ESR). IC50 of water-extracted MGX was found to be less than 225 μg mL(-1), in contrast with alkali-extracted MGX for which no radical scavenging was observed. Characterization of extracts by colorimetric assay, GC, LC-MS and NMR spectroscopy provided some clues to understanding structure-function relationships of MGX in connection with their antioxidant activity. Copyright © 2014 Elsevier B.V. All rights reserved.

Threat of plastic ageing in marine environment. Adsorption/desorption of micropollutants.

PubMed

Kedzierski, Mikaël; D'Almeida, Mélanie; Magueresse, Anthony; Le Grand, Adélaïde; Duval, Hélène; César, Guy; Sire, Olivier; Bruzaud, Stéphane; Le Tilly, Véronique

2018-02-01

Ageing of various plastics in marine environment was monitored after immersion of two synthetic (polyvinylchloride, PVC, and polyethylene terephthalate, PET) and one biodegradable (poly(butylene adipate co-terephtalate), PBAT) plastics for 502days in the bay of Lorient (Brittany, France). Data analysis indicates that aged PVC rapidly releases estrogenic compounds in seawater with a later adsorption of heavy metals; PET undergoes a low weakening of the surface whereas no estrogenic activity is detected; PBAT ages faster in marine environment than PVC. Aged PBAT exhibits heterogeneous surface with some cavities likely containing clay minerals from the chlorite group. Besides, this degraded material occasionally shows a high estrogenic activity. Overall, this study reports, for the first time, that some aged plastics, without being cytotoxic, can release estrogenic compounds in marine environment. Copyright © 2017. Published by Elsevier Ltd.

Influence of microwaves on the leaching kinetics of uraninite from a low grade ore in dilute sulfuric acid.

PubMed

Madakkaruppan, V; Pius, Anitha; T, Sreenivas; Giri, Nitai; Sarbajna, Chanchal

2016-08-05

This paper describes a study on microwave assisted leaching of uranium from a low-grade ore of Indian origin. The host rock for uranium mineralization is chlorite-biotite-muscovite-quartzo-feldspathic schist. The dominant presence of siliceous minerals determined leaching of uranium values in sulfuric acid medium under oxidizing conditions. Process parametric studies like the effect of sulfuric acid concentration (0.12-0.50M), redox potential (400-500mV), particle size (600-300μm) and temperature (35°-95°C) indicated that microwave assisted leaching is more efficient in terms of overall uranium dissolution, kinetics and provide relatively less impurities (Si, Al, Mg and Fe) in the leach liquor compared to conventional conductive leaching. The kinetics of leaching followed shrinking core model with product layer diffusion as controlling mechanism. Copyright © 2016 Elsevier B.V. All rights reserved.

Hydrothermal alteration maps of the central and southern Basin and Range province of the United States compiled from Advanced Spaceborne Thermal Emission and Reflection Radiometer (ASTER) data

USGS Publications Warehouse

Mars, John L.

2013-01-01

Advanced Spaceborne Thermal Emission and Reflection Radiometer (ASTER) data and Interactive Data Language (IDL) logical operator algorithms were used to map hydrothermally altered rocks in the central and southern parts of the Basin and Range province of the United States. The hydrothermally altered rocks mapped in this study include (1) hydrothermal silica-rich rocks (hydrous quartz, chalcedony, opal, and amorphous silica), (2) propylitic rocks (calcite-dolomite and epidote-chlorite mapped as separate mineral groups), (3) argillic rocks (alunite-pyrophyllite-kaolinite), and (4) phyllic rocks (sericite-muscovite). A series of hydrothermal alteration maps, which identify the potential locations of hydrothermal silica-rich, propylitic, argillic, and phyllic rocks on Landsat Thematic Mapper (TM) band 7 orthorectified images, and geographic information systems shape files of hydrothermal alteration units are provided in this study.

Organic matter diagenesis as the key to a unifying theory for the genesis of tabular uranium-vanadium deposits in the Morrison Formation, Colorado Plateau

USGS Publications Warehouse

Hansley, P.L.; Spirakis, C.S.

1992-01-01

Interstitial, epigenetic amorphous organic matter is intimately associated with uranium in the Grants uranium region and is considered essential to genetic models for these deposits. In contrast, uranium minerals are intimately associated with authigenic vanadium chlorite and vanadium oxides in amorphous organic matter-poor ores of the Slick Rock and Henry Mountains mining districts and therefore, in some genetic models amorphous organic matter is not considered crucial to the formation of these deposits. Differences in organic matter content can be explained by recognizing that amorphous organic matter-poor deposits have been subjected to more advanced stages of diagenesis than amorphous organic matter-rich deposits. Evidence that amorphous organic matter was involved in the genesis of organic matter-poor, as well as organic matter-rich, deposits is described. -from Authors

Potential of using multiscale kenaf fibers as reinforcing filler in cassava starch-kenaf biocomposites.

PubMed

Zainuddin, Siti Yasmine Zanariah; Ahmad, Ishak; Kargarzadeh, Hanieh; Abdullah, Ibrahim; Dufresne, Alain

2013-02-15

Biodegradable materials made from cassava starch and kenaf fibers were prepared using a solution casting method. Kenaf fibers were treated with NaOH, bleached with sodium chlorite and acetic buffer solution, and subsequently acid hydrolyzed to obtain cellulose nanocrystals (CNCs). Biocomposites in the form of films were prepared by mixing starch and glycerol/sorbitol with various filler compositions (0-10 wt%). X-ray diffraction revealed that fiber crystallinity increased after each stage of treatment. Morphological observations and size reductions of the extracted cellulose and CNCs were studied using field emission scanning electron microscopy and transmission electron microscopy. The effects of different treatments and filler contents of the biocomposites were evaluated through mechanical tests. Results showed that the tensile strengths and moduli of the biocomposites increased after each treatment and the optimum filler content was 6%. Copyright © 2012 Elsevier Ltd. All rights reserved.

Metamorphism, argon depletion, heat flow and stress on the Alpine fault

NASA Technical Reports Server (NTRS)

Scholz, C. H.; Beavan, J.; Hanks, T. C.

1978-01-01

The Alpine fault of New Zealand is a major continental transform fault which was uplifted on its southeast side 4 to 11 km within the last 5 m.y. This uplift has exposed the Haast schists, which were metamorphosed from the adjacent Torlesse graywackes. The Haast schists increase in metamorphic grade from prehnite-pumpellyite facies 9-12 km from the fault through the chlorite and biotite zones of the greenschist facies to the garnet-oligoclase zone amphibolite facies within 4 km of the fault. These metamorphic zone boundaries are subparallel to the fault for 350 km along the strike. The K-Ar and Rb-Sr ages of the schists increase with distance from the fault: from 4 m.y. within 3 km of the fault to approximately 110 m.y. 20 km from the fault. Field relations show that the source of heat that produced the argon depletion aureole was the fault itself.

Analysis of the Importance of Oxides and Clays in Cd, Cr, Cu, Ni, Pb and Zn Adsorption and Retention with Regression Trees

PubMed Central

González-Costa, Juan José; Reigosa, Manuel Joaquín; Matías, José María; Fernández-Covelo, Emma

2017-01-01

This study determines the influence of the different soil components and of the cation-exchange capacity on the adsorption and retention of different heavy metals: cadmium, chromium, copper, nickel, lead and zinc. In order to do so, regression models were created through decision trees and the importance of soil components was assessed. Used variables were: humified organic matter, specific cation-exchange capacity, percentages of sand and silt, proportions of Mn, Fe and Al oxides and hematite, and the proportion of quartz, plagioclase and mica, and the proportions of the different clays: kaolinite, vermiculite, gibbsite and chlorite. The most important components in the obtained models were vermiculite and gibbsite, especially for the adsorption of cadmium and zinc, while clays were less relevant. Oxides are less important than clays, especially for the adsorption of chromium and lead and the retention of chromium, copper and lead. PMID:28072849

The effect of non-structural components and lignin on hemicellulose extraction.

PubMed

Liu, Kai-Xuan; Li, Hong-Qiang; Zhang, Jie; Zhang, Zhi-Guo; Xu, Jian

2016-08-01

As the important structural component of corn stover, hemicellulose could be converted into a variety of high value-added products. However, high quality hemicellulose extraction is not an easy issue. The present study aims to investigate the effects of non-structural components (NSCs) and lignin removal on alkaline extraction of hemicellulose. Although NSCs were found to have a minimal effect on hemicellulose dissolution, they affected the color values of the hemicellulose extracts. The lignin limited the hemicellulose dissolution and increased the color value by binding to hemicellulose molecules and forming lignin-carbohydrate complexes. Sodium chlorite method can remove about 90% lignin from corn stover, especially the lignin connected to hemicellulose through p-coumaric and ferulic acids. Which increased the hemicellulose dissolution ratio to 93% and reduced the color value 14-28%, but the cost is about 20% carbohydrates lost. Copyright © 2016 Elsevier Ltd. All rights reserved.

Petrology of Impact-Melt Rocks at the Chicxulub Multiring Basin, Yucatan, Mexico

NASA Technical Reports Server (NTRS)

Schuraytz, Benjamin C.; Sharpton, Virgil L.; Marin, Luis E.

1994-01-01

Compositions and textures of melt rocks from the upper part of the Chicxulub structure are typical of melt rocks at other large terrestrial impact structures. Apart from variably elevated iridium concentrations (less than 1.5 to 13.5 +/- 0.9 ppb) indicating nonuniform dissemination of a meteoritic component, bulk rock and phenocryst compositions imply that these melt rocks were derived exclusively from continental crust and platform-sediment target lithologies. Modest differences in bulk chemistry among samples from wells located approximately 40 km apart suggest minor variations in relative contributions of these target lithologies to the melts. Subtle variations in the compositions of early-formed pyroxene and plagioclase also support minor primary differences in chemistry between the melts. Evidence for pervasive hydrothermal alteration of the porous mesostasis includes albite, K-feldspar, quartz, epidote, chlorite, and other phyllosilicates, as well as siderophile element-enriched sulfides, suggesting the possibility that Chicxulub, like Sudbury, may host important ore deposits.

Lake-sediment evidence for the date of deglaciation of the Hidden Lake area, Kenai Peninsula, Alaska

NASA Astrophysics Data System (ADS)

Rymer, Michael J.; Sims, John D.

1982-06-01

An abrupt environmental change is reflected in a core from Hidden Lake, Alaska, by differences in sediment type, chlorite crystallinity, and content of organic carbon and water of the sediments. This abrupt change in the sedimentary record occurred about 14,500 14C yr ago and probably marks the time of recession of the glacier from the Hidden Lake drainage basin. Deglaciation of the area was then underway, and rock flour was being deposited in the lake. After recession of the glacier from the Hidden Lake drainage basin, rock flour was no longer introduced, and organic-matter content of the sediment increased. By the dating of these changes in sediment type, we show that retreat of glaciers in this area took place significantly earlier than previously estimated; this agrees with the timing of retreat of alpine glaciers elsewhere in western North America.

Weathering Characteristics of Wood Plastic Composites Reinforced with Extracted or Delignified Wood Flour

PubMed Central

Chen, Yao; Stark, Nicole M.; Tshabalala, Mandla A.; Gao, Jianmin; Fan, Yongming

2016-01-01

This study investigated weathering performance of an HDPE wood plastic composite reinforced with extracted or delignified wood flour (WF). The wood flour was pre-extracted with three different solvents, toluene/ethanol (TE), acetone/water (AW), and hot water (HW), or sodium chlorite/acetic acid. The spectral properties of the composites before and after artificial weathering under accelerated conditions were characterized by Fourier transform infrared (FTIR) spectroscopy, the surface color parameters were analyzed using colorimetry, and the mechanical properties were determined by a flexural test. Weathering of WPC resulted in a surface lightening and a decrease in wood index (wood/HDPE) and flexural strength. WPCs that were reinforced with delignified wood flour showed higher ΔL* and ΔE* values, together with lower MOE and MOR retention ratios upon weathering when compared to those with non-extracted control and extracted WF. PMID:28773732

Methods for enhancing mapping of thermal fronts in oil recovery

DOEpatents

Lee, David O.; Montoya, Paul C.; Wayland, Jr., James R.

1987-01-01

A method for enhancing the resistivity contrasts of a thermal front in an oil recovery production field as measured by the CSAMT technique is disclosed. This method includes the steps of: (a) preparing a CSAMT-determined topological resistivity map of the production field; (b) introducing a solution of a dopant material into the production field at a concentration effective to alter the resistivity associated with the thermal front; said dopant material having a high cation exchange capacity which might be selected from the group consisting of montmorillonite, illite, and chlorite clays; said material being soluble in the connate water of the production field; (c) preparing a CSAMT-determined topological resistivity map of the production field while said dopant material is moving therethrough; and (d) mathematically comparing the maps from step (a) and step (c) to determine the location of the thermal front. This method is effective with the steam flood, fire flood and water flood techniques.

Soap-stone in architecture of North European cities. A nomination as a candidate for a Global Heritage Stones Resource

NASA Astrophysics Data System (ADS)

Bulakh, Andrey

2016-04-01

Soap stone represents soft Proterozoic rock type from the deposit Nunnalahti situated on the western shore of the big Lake Pielinen in Eastern Finland. It consists of talc (40 - 50 %), magnesite MgCO3 (40 - 50 %), chlorite (5 - 8 %), dolomite, calcite, etc. The colour of the stone is very spectacular and varies from yellow and brownish-yellow to grey, greenish grey. The soft stone is a highly workable material for a sculptor's chisel. It was one of the most popular ornamental rocks used architecture of the Modern style in St Petersburg, Helsinki, Turku, Tampere and other North European cities lately in the XIX-th centuries. Examples are given and discussed. References: Bulakh, A.G., Abakumova, N.B., and Romanovsky, J.V. St Petersburg: a History in Stone. 2010. Print House of St Petersburg State University. 173 p. (In English).

Isolation and characterization of autotrophic, hydrogen-utilizing, perchlorate-reducing bacteria.

PubMed

Shrout, Joshua D; Scheetz, Todd E; Casavant, Thomas L; Parkin, Gene F

2005-04-01

Recent studies have shown that perchlorate (ClO(4) (-)) can be degraded by some pure-culture and mixed-culture bacteria with the addition of hydrogen. This paper describes the isolation of two hydrogen-utilizing perchlorate-degrading bacteria capable of using inorganic carbon for growth. These autotrophic bacteria are within the genus Dechloromonas and are the first Dechloromonas species that are microaerophilic and incapable of growth at atmospheric oxygen concentrations. Dechloromonas sp. JDS5 and Dechloromonas sp. JDS6 are the first perchlorate-degrading autotrophs isolated from a perchlorate-contaminated site. Measured hydrogen thresholds were higher than for other environmentally significant, hydrogen-utilizing, anaerobic bacteria (e.g., halorespirers). The chlorite dismutase activity of these bacteria was greater for autotrophically grown cells than for cells grown heterotrophically on lactate. These bacteria used fumarate as an alternate electron acceptor, which is the first report of growth on an organic electron acceptor by perchlorate-reducing bacteria.

Water and Sediment Quality in the Yukon River Basin, Alaska, During Water Year 2005

DTIC Science & Technology

2007-01-01

Disordered Kaolinite 0.6 0.5 0.4 0.7 0.6 1.0 0.4 Ferruginous smectite 7.4 9.5 6.1 4.9 9.4 10.6 12.4 Illite + Smectite 6.8 4.8 5.2 6.6 6.6 5.5 4.9...64.7 Clays: Goethite 0.1 0.1 0.3 0.1 0.1 0.3 0.1 Disordered Kaolinite 0.6 0.9 0.3 0.7 0.9 0.6 0.7 Ferruginous smectite 7.0 6.8 7.1...7.9 7.6 16.4 15.7 Illite + Smectite 10.2 7.7 8.1 7.9 6.8 1.2 3.2 Chlorite 8.0 9.5 9.6 9.4 10.7 10.8 12.2 Muscovite (2M1) 4.1 6.0 5.2 4.8 4.1 4.8

Mineralogy and geochemistry of Eocene Helete formation , Adiyaman, Turkey

NASA Astrophysics Data System (ADS)

Choi, J.; Lee, I.; Yildirim, E.

2013-12-01

Helete formation is located at Adiyaman, Turkey which is in the Alpine-Himalayan orogeny belt. Helete formation is represented by andesitic, basaltic and gabbroic rocks cut by localized felsic intrusions and overlain by open-marine Nummulitic carbonate sediments. Electron microprobe analyses were conducted for 15 rocks samples of Helete formation. These rock samples are named as basalt, andesite, gabbro, diorite, dacite, and granite. Basalt and andesite samples are composed of clinopyroxene(augite), plagioclase(Ab98-96), carbonate, and hyaline. Gabbro samples have wide range of plagioclase composition from anorthite to albite(Ab92-16), and other minerals like clinopyroxene(augite) and amphibole(hornblende and actinolite). Diabase samples consist of epidote group minerals and sphene with plagioclase(Ab80), pyroxene and hornblende. Dacite samples are composed of dolomite and quartz. Granite samples are composed of quartz, chlorite, and plagioclase which range from albite to oligoclase in composition (Ab98-89).

Chemometric analysis of the consumption of oral rinse chlorite (ClO2-) by human salivary biomolecules.

PubMed

Chang, Hubert; Blackburn, John; Grootveld, Martin

2013-12-01

Oral rinse formulations containing chlorite anion (ClO(2)(-)) as an active agent exert a range of valuable oral healthcare activities. However, salivary biomolecules which chemically react with this oxidant can, at least in principle, serve as potentially significant barriers to these therapeutic properties in the oral environment. Therefore, in this investigation, we have explored the extent of ClO(2)(-) consumption by biomolecules which scavenge this agent in human salivary supernatants (HSSs) in vitro. HSS samples were equilibrated with oral rinse formulations containing this active agent (30 s at 35 °C in order to mimic oral rinsing episodes). Differential spectrophotometric and ion-pair reversed-phase high-performance liquid chromatographic analyses were employed to determine residual ClO(2)(-) in these admixtures. Bioanalytical data acquired revealed the rapid consumption of ClO(2)(-) by biomolecular electron donors and/or antioxidants present in HSS samples. Mean ± 95 % confidence interval (CI) consumption levels of 7.14 ± 0.69 and 5.34 ± 0.69 % of the total ClO(2)(-) available were found for oral rinse products containing 0.10 and 0.40 % (w/v) ClO(2)(-), respectively. A mixed model analysis-of-variance performed on experimental data acquired demonstrated highly-significant differences between oral rinse ClO(2)(-) contents (p < 0.0001), trial participants (p < 0.001) and sampling days-within-participants (p < 0.001), and also revealed non-additive ClO(2)(-)-scavenging responses of participants' HSSs to increases in the oral rinse content of this oxidant (p < 0.0001). A slower, second phase of the reaction process (t (1/2) = 1.7-2.8 h) involved the oxidative consumption of salivary urate. These data clearly demonstrate that for recommended 30 s oral rinsing episodes performed at physiological temperature, <10 % of the total oral rinse ClO(2)(-) available is chemically and/or reductively consumed by HSS biomolecules for both oral rinse formulations investigated. These observations are of much clinical significance in view of the retention of these products' active agent, i.e. <10 % of ClO(2)(-) is consumed by HSS biomolecules within recommended 30 s oral rinsing episodes, and hence, the bulk of this oxyhalogen oxidant (>90 %) may effectively exert its essential microbicidal, anti-periodontal and oral malodour-neutralising actions.

Structure and water exchange dynamics of hydrated oxo halo ions in aqueous solution using QMCF MD simulation, large angle X-ray scattering and EXAFS.

PubMed

Eklund, Lars; Hofer, Tomas S; Persson, Ingmar

2015-01-28

Theoretical ab initio quantum mechanical charge field molecular dynamics (QMCF MD) has been applied in conjunction with experimental large angle X-ray scattering (LAXS) and EXAFS measurements to study structure and dynamics of the hydrated oxo chloro anions chlorite, ClO2(-), chlorate, ClO3(-), and perchlorate, ClO4(-). In addition, the structures of the hydrated hypochlorite, ClO(-), bromate, BrO3(-), iodate, IO3(-) and metaperiodate, IO4(-), ions have been determined in aqueous solution by means of LAXS. The structures of the bromate, metaperiodate, and orthoperiodate, H2IO6(3-), ions have been determined by EXAFS as solid sodium salts and in aqueous solution as well. The results show clearly that the only form of periodate present in aqueous solution is metaperiodate. The Cl-O bond distances in the hydrated oxo chloro anions as determined by LAXS and obtained in the QMCF MD simulations are in excellent agreement, being 0.01-0.02 Å longer than in solid anhydrous salts due to hydration through hydrogen bonding to water molecules. The oxo halo anions, all with unit negative charge, have low charge density making them typical structure breakers, thus the hydrogen bonds formed to the hydrating water molecules are weaker and more short-lived than those between water molecules in pure water. The water exchange mechanism of the oxo chloro anions resembles those of the oxo sulfur anions with a direct exchange at the oxygen atoms for perchlorate and sulfate. The water exchange rate for the perchlorate ion is significantly faster, τ0.5 = 1.4 ps, compared to the hydrated sulfate ion and pure water, τ0.5 = 2.6 and 1.7 ps, respectively. The angular radial distribution functions show that the chlorate and sulfite ions have a more complex water exchange mechanism. As the chlorite and chlorate ions are more weakly hydrated than the sulfite ion the spatial occupancy is less well-defined and it is not possible to follow any well-defined migration pattern as it is difficult to distinguish between hydrating water molecules and bulk water in the region close to the ions.

Records of near-isothermal decompression and clockwise P-T history from the Paleoproterozoic Mahakoshal Belt, Central Indian Tectonic Zone: Constraints from pseudosection modelling and monazite geochronology

NASA Astrophysics Data System (ADS)

Deshmukh, Tanzil; Naraga, Prabhakar; Bhattacharya, Abhijit; Kaliappan, Madhavan

2017-04-01

The Mahakoshal Belt (MB) is regarded as the oldest subunit along the northern collar of the Central Indian Tectonic Zone (CITZ) arguably representing the zone of accretion between the North India Block and the South India Block. The following study focuses on deciphering the structural and metamorphic P-T-t history of the schists/phyllites from the eastern part of the belt, and provides insights into the Paleoproterozoic tectonic development in the CITZ. The schists comprise phengite, quartz, andalusite, biotite, muscovite and margarite, and are associated with veins of rare andalusite + corundum + quartz assemblage. The field relations combined with deformation microtextures in the MB schists suggests three episodes of metamorphism, M1, M2 and M3, corresponding with D1, D2 and D3 deformation events respectively. Inclusion trails (S1) of phengite + biotite + quartz ± chlorite in syn/post-S2 andalusite porphyroblasts constrain the M1 metamorphic event in pelitic schists. The application of pseudosection modelling estimated peak metamorphic conditions at ˜8 kbar and 520 ˚ C. Near isothermal decompression (<4 kbar) resulted in the formation of the andalusite + muscovite bearing retrograde assemblage that stabilized at the expense of phengite-bearing assemblage. Further, andalusite porphyroblasts are replaced by margarite + muscovite + chlorite pseudomorphs (2-3 kbar) during syn/post-S3 fluid-aided metamorphism. Th-U-total Pb dating of monazite grains yield core populations at 1.8-1.9 Ga, and rim populations at 1.7-1.8 Ga and 1.5-1.6 Ga. Thus, the peak metamorphism in MB schists was Paleoproterozoic in age, 1.8-1.9 Ga, and the clockwise P-T path was recorded at 1.7-1.8 Ga, which overlaps with the emplacement of blastoporphyritic granitoids along southern margin of the MB. The results obtained in this study combined with the existing structural-metamorphic-chronological information demonstrate the CITZ to be a composite of desperately-evolved crustal domains. With some major omissions, the tectono-thermal events identified in the CITZ partly overlap with those observed in the Capricorn Orogen (Western Australia) and the Trans North China Orogen. Therefore, these global correlations possibly corroborate new configurations on the assembly and fragmentation of Columbia Supercontinent, but await further studies and robust age determinations in the various parts of CITZ.

Porosity evolution during weathering of Marcellus shale

NASA Astrophysics Data System (ADS)

Gu, X.; Brantley, S.

2017-12-01

Weathering is an important process that continuously converts rock to regolith. Shale weathering is of particular interest because 1) shale covers about 25% of continental land mass; 2) recent development of unconventional shale gas generates large volumes of rock cuttings. When cuttings are exposed at earth's surface, they can release toxic trace elements during weathering. In this study, we investigated the evolution of pore structures and mineral transformation in an outcrop of Marcellus shale - one of the biggest gas shale play in North America - at Frankstown, Pennsylvania. A combination of neutron scattering and imaging was used to characterize the pore structures from nm to mm. The weathering profile of Marcellus shale was also compared to the well-studied Rose Hill shale from the Susquehanna Shale Hills critical zone observatory nearby. This latter shale has a similar mineral composition as Marcellus shale but much lower concentrations of pyrite and OC. The Marcellus shale formation in outcrop overlies a layer of carbonate at 10 m below land surface with low porosity (<3%). All the shale samples above the carbonate layer are almost completely depleted in carbonate, plagioclase, chlorite and pyrite. The porosities in the weathered Marcellus shale are twice as high as in protolith. The pore size distribution exhibits a broad peak for pores of size in the range of 10s of microns, likely due to the loss of OC and/or dissolution of carbonate during weathering. In the nearby Rose Hill shale, the pyrite and carbonate are sharply depleted close to the water table ( 15-20 m at ridgetop); while chlorite and plagioclase are gradually depleted toward the land surface. The greater weathering extent of silicates in the Marcellus shale despite the similarity in climate and erosion rate in these two neighboring locations is attributed to 1) the formation of micron-size pores increases the infiltration rate into weathered Marcellus shale and therefore promotes mineral weathering; 2) the pyrite/carbonate ratio is higher in the Marcellus shale than in Rose Hill shale, and thus excess acidity generated through pyrite oxidation enhances the dissolution of silicates. We seek to use these and other observations to develop a global model for shale weathering that incorporates both mineral composition and porosity change.

Pre-impact tectonothermal evolution of the crystalline basement-derived rocks in the ICDP-USGS Eyreville B core, Chesapeake Bay impact structure

USGS Publications Warehouse

Gibson, R.L.; Townsend, G.N.; Horton, J. Wright; Reimold, W.U.

2009-01-01

Pre-impact crystalline rocks of the lowermost 215 m of the Eyreville B drill core from the Chesapeake Bay impact structure consist of a sequence of pelitic mica schists with subsidiary metagraywackes or felsic metavolcanic rocks, amphibolite, and calc-silicate rock that is intruded by muscovite (??biotite, garnet) granite and granite pegmatite. The schists are commonly graphitic and pyritic and locally contain plagioclase porphyroblasts, fi brolitic sillimanite, and garnet that indicate middle- to upper-amphibolite-facies peak metamorphic conditions estimated at ??0.4-0.5 GPa and 600-670 ??C. The schists display an intense, shallowly dipping, S1 composite shear foliation with local micrometer- to decimeter-scale recumbent folds and S-C' shear band structures that formed at high temperatures. Zones of chaotically oriented foliation, resembling breccias but showing no signs of retrogression, are developed locally and are interpreted as shear-disrupted fold hinges. Mineral textural relations in the mica schists indicate that the metamorphic peak was attained during D1. Fabric analysis indicates, however, that subhorizontal shear deformation continued during retrograde cooling, forming mylonite zones in which high-temperature shear fabrics (S-C and S-C') are overprinted by progressively lower- temperature fabrics. Cataclasites and carbonate-cemented breccias in more competent lithologies such as the calc-silicate unit and in the felsic gneiss found as boulders in the overlying impactite succession may refl ect a fi nal pulse of low-temperature cataclastic deformation during D1. These breccias and the shear and mylonitic foliations are cut by smaller, steeply inclined anastomosing fractures with chlorite and calcite infill (interpreted as D2). This D2 event was accompanied by extensive chlorite-sericitecalcite ?? epidote retrogression and appears to predate the impact event. Granite and granite pegmatite veins display local discordance to the S1 foliation, but elsewhere they are affected by high-temperature mylonitic shear deformation, suggesting a late-D1 intrusive timing close to the metamorphic peak. The D1 event is tentatively interpreted as a thrusting event associated with westward-verging collision between Gondwana and Laurentia before or during the Permian-Carboniferous Alleghanian orogeny. It is unclear whether subsequent brittle deformation, described here as D2, could be part of regional dextral Alleghanian strike-slip faulting or younger Mesozoic normal faulting. ?? 2009 The Geological Society of America.

Provenance analysis of heavy minerals in beach sands (Falkland Islands/Islas Malvinas) - A view to mineral deposits and the geodynamics of the South Atlantic Ocean

NASA Astrophysics Data System (ADS)

Dill, Harald G.; Skoda, Radek

2017-10-01

Beach sands are ideal traps to collect heavy minerals (HM) from different geodynamic settings and mineral deposits. The coastal sediments contain a mixture of HM derived from the submarine shelf and from source rocks in the hinterland. This is true in a transgressive periglacial regime, where drowned valleys and estuaries are instrumental in draining HM to the arenaceous beach sediments from more distal basement lithologies. A scenario like this can be found in the Falkland Islands/Islas Malvinas. The site under study is the missing link between South Africa and South America, the splitting-apart of which is mirrored by the HM distribution predominantly concentrated in the backshore and dune belt along the coast. The HM are subdivided into three HM associations reflecting the geodynamic evolution of the South Atlantic Ocean and of some of the prominent mineral deposits on the Gondwana Continent: (1) Gondwana cratons and Proterozoic orogens, with Cr and BIF deposits (rutile, zircon, ilmenite, tourmaline, garnet, Cr spinel), (2) rift-related and break-apart magmatic lithologies with mantle-derived pipe rocks such as kimberlites (zircon, pyroxene, spinel, Mg ilmenite), (3) Cordillera-type lithologies with polymetallic stratabound deposits (tourmaline, amphibole, chlorite, REE phosphates). The variation of the major HM from the stable craton (Kalahari-Kaapvaal Craton) in the East to the mobile fold belt (Andes) in the West follows the order of stability of HM. In addition to these 3 geodynamic HM groups, sporadic occurrences of HM originating from alteration (leucoxene, chlorite s.s.s. (= solid solution series)) are part of armored relics such as "nigrine" which on transport disintegrated and thereby released these HM. The major ultrastable and stable HM zircon, rutile, tourmaline s.s.s., spinel s.s.s., and garnet s.s.s. are displayed in a synoptical x-y plot showing the mantle and crustal trends of fractionation and formation of cumulates by means of particular mineral associations as well as the chemical composition of their s.s.s. Five different geodynamic-lithological patterns, each represented by a set of type-lithologies are established for the cratonic magmatic-metamorphic lithosphere. Based on the HM, the geodynamic setting under study is dominated by source rocks typical of a primitive, cratonic setting.

The in vitro reduction of sodium [36Cl]chlorate in bovine ruminal fluid.

PubMed

Oliver, C E; Bauer, M L; Caton, J S; Anderson, R C; Smith, D J

2007-08-01

Sodium chlorate effectively reduces or eliminates gram-negative pathogenic bacteria in the gastrointestinal tracts of live cattle. Limitations to the in vivo efficacy of chlorate are its rapid absorption from the gastrointestinal tract and its presumed reduction to chloride within the gastrointestinal tract. We hypothesized that chlorate would be reduced via ruminal bacteria in a ruminal in vitro system and that the reduction of chlorate would be influenced by the dietary for-age:concentrate ratio; thus, 4 ruminally cannulated steers were fed 20 or 80% concentrate diets in a crossover design. Ruminal fluid was collected in 2 periods and dispensed into in vitro tubes containing sodium [36Cl]chlorate, which was sufficient for 100 or 300 mg/L final chlorate concentrations. The tubes were incubated for 0, 1, 4, 8, 16, or 24 h; autoclaved, control ruminal fluid, fortified with sodium [36Cl]chlorate, was incubated for 24 h. Chlorate remaining in each sample was measured by liquid scintillation counting after [36Cl]chloride was precipitated with silver nitrate. A preliminary study indicated that chlorite, a possible intermediate in the reduction of chlorate, had a half-life of approximately 4.5 min in freshly collected (live) ruminal fluid; chlorite was, therefore, not specifically measured in ruminal incubations. The chlorate dose did not affect in vitro DM digestion (P > or = 0.11), whereas in vitro DM digestibility was decreased (P < or = 0.05) by 80% forage content. By 24 h, 57.5 +/- 2.6% of the chlorate remained in 100-mg/L incubations, whereas 78.2 +/- 2.6% of the chlorate remained in the 300-mg/L incubations. When the data were expressed on a concentration basis (mg/L), diet had no effect (P > or = 0.18) on chlorate reduction; however, when chlorate reduction was expressed on a percentage basis, chlorate reduction tended to be greater (P > or = 0.09) at 8 and 16 h in the incubations containing the low-concentrate diet. Chlorate remaining in autoclaved controls at 24 h was intermediate (P < 0.01) between chlorate remaining in live ruminal fluid samples incubated for 0 or 24 h. Attempts to isolate chlorate-respiring bacteria from 2 sources of ruminal fluid were not successful. These data indicate that microbial-dependent or chemical-dependent, or both, reduction of chlorate occurs in bovine ruminal fluid and that dietary concentrate had a negligible effect on chlorate reduction.

Late Ordovician (Ashgillian) glacial deposits in southern Jordan

NASA Astrophysics Data System (ADS)

Turner, Brian R.; Makhlouf, Issa M.; Armstrong, Howard A.

2005-11-01

The Late Ordovician (Ashgillian) glacial deposits in southern Jordan, comprise a lower and upper glacially incised palaeovalley system, occupying reactivated basement and Pan-African fault-controlled depressions. The lower palaeovalley, incised into shoreface sandstones of the pre-glacial Tubeiliyat Formation, is filled with thin glaciofluvial sandstones at the base, overlain by up to 50 m of shoreface sandstone. A prominent glaciated surface near the top of this palaeovalley-fill contains intersecting glacial striations aligned E-W and NW-SE. The upper palaeovalley-fill comprises glaciofluvial and marine sandstones, incised into the lower palaeovalley or, where this is absent, into the Tubeiliyat Formation. Southern Jordan lay close to the margin of a Late Ordovician terrestrial ice sheet in Northwest Saudi Arabia, characterised by two major ice advances. These are correlated with the lower and upper palaeovalleys in southern Jordan, interrupted by two subsidiary glacial advances during late stage filling of the lower palaeovalley when ice advanced from the west and northwest. Thus, four ice advances are now recorded from the Late Ordovician glacial record of southern Jordan. Disturbed and deformed green sandstones beneath the upper palaeovalley-fill in the Jebel Ammar area, are confined to the margins of the Hutayya graben, and have been interpreted as structureless glacial loessite or glacial rock flour. Petrographic and textural analyses of the deformed sandstones, their mapped lateral transition into undeformed Tubeiliyat marine sandstones away from the fault zone, and the presence of similar sedimentary structures to those in the pre-glacial marine Tubeiliyat Formation suggest that they are a locally deformed facies equivalent of the Tubeiliyat, not part of the younger glacial deposits. Deformation is attributed to glacially induced crustal stresses and seismic reactivation of pre-existing faults, previously weakened by epeirogenesis, triggering sediment liquefaction and deformation typical of earthquake generated seismites. Deformation, confined to an area of not more than 4 km wide adjacent to the major fault zone, implies earthquake magnitudes of at least 6 (M o). The high authigenic chlorite content of deformed Tubeiliyat sandstones compared to undeformed ones is attributed to a post-seismic hydrothermal system driven by compactional dewatering and hydrofracturing of the bedrock which acted as a groundwater recharge area, supplied by subglacial meltwater from beneath the ice sheet. Fluid movement along glacial seismotectonically reactivated faults infiltrated the adjacent Tubeiliyat sandstones under pressure and elevated geothermal gradient, where chlorite was precipitated from solution.

Structure and water exchange dynamics of hydrated oxo halo ions in aqueous solution using QMCF MD simulation, large angle X-ray scattering and EXAFS

PubMed Central

Eklund, Lars; Hofer, Tomas S.

2014-01-01

Theoretical ab initio quantum mechanical charge field molecular dynamics (QMCF MD) has been applied in conjunction with experimental large angle X-ray scattering (LAXS) and EXAFS measurements to study structure and dynamics of the hydrated oxo chloro anions chlorite, ClO2−, chlorate, ClO3−, and perchlorate, ClO4−. In addition, the structures of the hydrated hypochlorite, ClO−, bromate, BrO3−, iodate, IO3− and metaperiodate, IO4−, ions have been determined in aqueous solution by means of LAXS. The structures of the bromate, metaperiodate, and orthoperiodate, H2IO63−, ions have been determined by EXAFS as solid sodium salts and in aqueous solution as well. The results show clearly that the only form of periodate present in aqueous solution is metaperiodate. The Cl-O bond distances in the hydrated oxo chloro anions as determined by LAXS and obtained in the QMCF MD simulations are in excellent agreement, being 0.01–0.02 Å longer than in solid anhydrous salts due to hydration through hydrogen bonding to water molecules. The oxo halo anions, all with unit negative charge, have low charge density making them typical structure breakers, thus the hydrogen bonds formed to the hydrating water molecules are weaker and more short-lived than those between water molecules in pure water. The water exchange mechanism of the oxo chloro anions resembles those of the oxo sulfur anions with a direct exchange at the oxygen atoms for perchlorate and sulfate. The water exchange rate for the perchlorate ion is significantly faster, τ0.5=1.4 ps, compared to the hydrated sulfate ion and pure water, τ0.5=2.6 and 1.7 ps, respectively. The angular radial distribution functions show that the chlorate and sulfite ions have a more complex water exchange mechanism. As the chlorite and chlorate ions are more weakly hydrated than the sulfite ion the spatial occupancy is less well-defined and it is not possible to follow any well-defined migration pattern as it is difficult to distinguish between hydrating water molecules and bulk water in the region close to the ions. PMID:25473816

Structure and water exchange dynamics of hydrated oxo halo ions in aqueous solution using QMCF MD simulation, large angle X-ray scattering and EXAFS

DOE PAGES

Eklund, Lars; Hofer, Tomas S.; Persson, Ingmar

2014-11-26

Theoretical ab initio quantum mechanical charge field molecular dynamics (QMCF MD) has been applied in conjunction with experimental large angle X-ray scattering (LAXS) and EXAFS measurements to study structure and dynamics of the hydrated oxo chloro anions chlorite, ClO 2 –, chlorate, ClO 3 –, and perchlorate, ClO 4 –. In addition, the structures of the hydrated hypochlorite, ClO –, bromate, BrO 3 –, iodate, IO 3 – and metaperiodate, IO 4 –, ions have been determined in aqueous solution by means of LAXS. The structures of the bromate, metaperiodate, and orthoperiodate, H 2IO 6 3–, ions have been determinedmore » by EXAFS as solid sodium salts and in aqueous solution as well. The results show clearly that the only form of periodate present in aqueous solution is metaperiodate. The Cl–O bond distances in the hydrated oxo chloro anions as determined by LAXS and obtained in the QMCF MD simulations are in excellent agreement, being 0.01–0.02 Å longer than in solid anhydrous salts due to hydration through hydrogen bonding to water molecules. The oxo halo anions, all with unit negative charge, have low charge density making them typical structure breakers, thus the hydrogen bonds formed to the hydrating water molecules are weaker and more short-lived than those between water molecules in pure water. The water exchange mechanism of the oxo chloro anions resembles those of the oxo sulfur anions with a direct exchange at the oxygen atoms for perchlorate and sulfate. Here, the water exchange rate for the perchlorate ion is significantly faster, τ 0.5 = 1.4 ps, compared to the hydrated sulfate ion and pure water, τ 0.5 = 2.6 and 1.7 ps, respectively. The angular radial distribution functions show that the chlorate and sulfite ions have a more complex water exchange mechanism. As the chlorite and chlorate ions are more weakly hydrated than the sulfite ion the spatial occupancy is less well-defined and it is not possible to follow any well-defined migration pattern as it is difficult to distinguish between hydrating water molecules and bulk water in the region close to the ions.« less

Experimental investigation of CO2-brine-rock interactions at simulated in-situ conditions

NASA Astrophysics Data System (ADS)

Słomski, Piotr; Lutyński, Marcin; Mastalerz, Maria; Szczepański, Jacek; Derkowski, Arkadiusz; Topór, Tomasz

2017-04-01

Geological sequestration of carbon dioxide (CO2) in deep formations (e.g. saline aquifers, oil and gas reservoirs and coalbeds) is one of the most promising options for reducing concentration of this anthropogenic greenhouse gas in the atmosphere. CO2 injected into the rock formations can be trapped by several mechanisms including structural and stratigraphic trapping, capillary CO2 trapping, dissolution trapping and mineral trapping. During dissolution trapping, CO2 dissolves in the formation brine and sinks in the reservoir as the CO2-enriched brine has an increased density. In comparison, in mineral trapping, CO2 is bound by precipitating new carbonate minerals. The latter two mechanisms depend on the temperature, pressure, and the mineralogy of the reservoir rock and the chemical composition of the brine. This study discusses laboratory scale alterations of Ordovician and Silurian shale rocks from potential CO2 sequestration site B1 in the Baltic Basin. In the reported experiment, rocks submerged in brine in specially constructed reactors were subjected to CO2 pressure of 30-35 MPa for 30-45 days at temperature of 80 oC. Shale samples were analyzed in terms of mineral composition and mesopore surface area and volume, before and after experiments, by means of X-ray diffraction and N2 low-pressure adsorption, respectively, for possible CO2 induced changes. Comparison of mineral composition before and after experiments demonstrated subtle mineral changes. The most conspicuous was a release of Fe in the form of Fe-oxyhydroxides, most probably related to the decomposition of Fe-bearing minerals like pyrite, chlorite and, less frequently, ankerite. With regard to porosity, interestingly, the most significant increase in mesopore surface area and mesopore volume was observed in samples with the largest drop of chlorite amount. The less significant mineral changes were associated with formation of kaolinite related to breakdown of feldspars and dissolution of carbonate minerals represented by calcite, dolomite, and ankerite. In the analyzed samples, no new carbonate minerals were formed during the experiments. An increase of carbonates was recorded only in three out of 13 samples. However, concentration of carbonates in these three samples is too low to conclude CO2 mineral trapping in new carbonate phases. Acknowledgments: the study was supported from grant SHALESEQ (No PL12-0109) funded by the National Centre for Research and Development.

Evidence for intense hydrothermal alteration associated with flood basalt volcanism during the birth of the Azores Plateau

NASA Astrophysics Data System (ADS)

Bach, W.; Busch, A.; Genske, F. S.; Beier, C.; Krumm, S.

2017-12-01

A stratigraphic section comprising >1000 m of upper crust in the Princess Alice Bank (PAB) of the western Azores Plateau was sampled during RV Meteor cruise M128 in July of 2016, using the ROV MARUM Quest 4000m. Twenty-two samples were recovered between 2484 and 1439 m water depth from the southfacing footwall of the Master fault bounding a prominent NW-SE striking rift zone within the PAB. Our geochemical and petrographic results show that virtually all samples are pervasively altered. The deeper part of the section (up to 1750 m water depth) was altered under greenschist-facies conditions to assemblages that include epidote, chlorite, albite, titanite, and actinolite. These rocks show 87Sr/86Sr values between 0.7036 and 0.7050. The topmost section was altered under lower metamorphic grades to chlorite/smectite-quartz-anatase. These rocks show severe losses of Ca and Sr, and gains in Mg, Li, and B, with 87Sr/86Sr ratios as high as 0.708. These geochemical signatures indicate an intensity of hydrothermal exchange between seawater and crust that is unmatched by any in situ section of upper ocean crust sampled by ocean drilling to date. Oxygen isotope data for epidote-calcite veins indicate temperatures of 250-300°C. Later quartz gives about 200°C. The implications of the intense hydrothermal alteration for crust-seawater exchange budgets can be evaluated in the light of the geological evolution of the PAB. Based on immobile element ratios of whole rocks and REE characteristics of relict clinopyroxene in the only incompletely altered sample, an E-type MORB primary composition of the basalts can be reconstructed. Our data suggest that the degrees of mantle melting were much higher than during extrusion of the <4 Ma old alkali-basalts recovered from the top of PAB (Beier et al., 2015, doi:10.1130/2015.2511(02)), and even higher than modern MORB at the adjacent mid-Atlantic Ridge. These results lead us to suggest that the deeper sections of the PAB formed during the initial stages of flood basalt activity. The extreme hydrothermal alteration may hence be directly linked to the prolonged magmatic period during which excess melting produced a 13-km thick igneous crust. Our results indicate that marine plateau-forming events may cause transient highs in hydrothermal flux rates.

Universal Immunoprobe for (Per)Chlorate-Reducing Bacteria

PubMed Central

O'Connor, Susan M.; Coates, John D.

2002-01-01

Recent studies in our lab have demonstrated the ubiquity and diversity of microorganisms which couple growth to the reduction of chlorate or perchlorate [(per)chlorate] under anaerobic conditions. We identified two taxonomic groups, the Dechloromonas and the Dechlorosoma groups, which represent the dominant (per)chlorate-reducing bacteria (ClRB) in the environment. As part of these studies we demonstrated that chlorite dismutation is a central step in the reductive pathway of (per)chlorate that is common to all ClRB and which is mediated by the enzyme chlorite dismutase (CD). Initial studies on CD suggested that this enzyme is highly conserved among the ClRB, regardless of their phylogenetic affiliation. As such, this enzyme makes an ideal target for a probe specific for these organisms. Polyclonal antibodies were commercially raised against the purified CD from the ClRB Dechloromonas agitata strain CKB. The obtained antiserum was deproteinated by ammonium sulfate precipitation, and the antigen binding activity was assessed using dot blot analysis of a serial dilution of the antiserum. The titers obtained with purified CD indicated that the antiserum had a high affinity for the CD enzyme, and activity was observed in dilutions as low as 10−6 of the original antiserum. The antiserum was active against both cell lysates and whole cells of D. agitata, but only if the cells were grown anaerobically with (per)chlorate. No response was obtained with aerobically grown cultures. In addition to D. agitata, dot blot analysis employed with both whole-cell suspensions and cell lysates of several diverse ClRB representing the alpha, beta, and gamma subclasses of Proteobacteria tested positive regardless of phylogenetic affiliation. Interestingly, the dot blot response obtained for each of the ClRB cell lysates was different, suggesting that there may be some differences in the antigenic sites of the CD protein produced in these organisms. In general, no reactions were observed with cells or cell lysates of the organisms closely related to the ClRB which could not grow by (per)chlorate reduction. These studies have resulted in the development of a highly specific and sensitive immunoprobe based on the commonality of the CD enzyme in ClRB which can be used to assess dissimilatory (per)chlorate-reducing populations in environmental samples regardless of their phylogenetic affiliations. PMID:12039773

Structural Characterization of the Foliated-Layered Gabbro Transition in Wadi Tayin of the Samail Ophiolite, Oman; Oman Drilling Project Holes GT1A and GT2A

NASA Astrophysics Data System (ADS)

Deans, J. R.; Crispini, L.; Cheadle, M. J.; Harris, M.; Kelemen, P. B.; Teagle, D. A. H.; Matter, J. M.; Takazawa, E.; Coggon, J. A.

2017-12-01

Oman Drilling Project Holes GT1A and GT2A were drilled into the Wadi Tayin massif, Samail ophiolite and both recovered ca. 400 m of continuous core through a section of the layered gabbros and the foliated-layered gabbro transition. Hole GT1A is cut by a discrete fault system including localized thin ultracataclastic fault zones. Hole GT2A is cut by a wider zone of brittle deformation and incipient brecciation. Here we report the structural history of the gabbros reflecting formation at the ridge to later obduction. Magmatic and high temperature history- 1) Both cores exhibit a pervasive, commonly well-defined magmatic foliation delineated by plagioclase, olivine and in places clinopyroxene. Minor magmatic deformation is present. 2) The dip of the magmatic foliation varies cyclically, gradually changing dip by 30o from gentle to moderate over a 50 m wavelength. 3) Layering is present throughout both cores, is defined by changes in mode and grain size ranging in thickness from 2 cm to 3 m and is commonly sub-parallel to the foliation. 4) There are no high temperature crystal-plastic shear zones in the core. Key observations include: no simple, systematic shallowing of dip with depth across the foliated-layered gabbro transition and layering is continuous across this transition. Cyclic variation of magmatic foliation dip most likely reflects the process of plate separation at the ridge axis. Near-axis faulting- i) On or near-axis structures consist of epidote-amphibole bearing hydraulic breccias and some zones of intense cataclasis with intensely deformed epidote and seams of clay and chlorite accompanied by syntectonic alteration of the wall rock. Early veins are filled with amphibole, chlorite, epidote, and anhydrite. ii) The deformation ranges from brittle-ductile, causing local deflection of the magmatic foliation, to brittle offset of the foliation and core and mantle structures in anhydrite veins. iii) The prevalent sense of shear is normal and slickenfibers indicate oblique offset. Obduction related faulting- i) Low temperature brittle faults and veins with laumontite, clay, and gypsum crosscut all structures. ii) Faults show a reverse sense of shear and crosscut, possibly reactivate, normal faults. Our observations suggest formation of reverse faults and late veins during obduction of the ophiolite.

Metamorphism Near the Dike-Gabbro Transition in the Ocean Crust Based on Preliminary Results from Oman Drilling Project Hole GT3A

NASA Astrophysics Data System (ADS)

Manning, C. E.; Nozaka, T.; Harris, M.; Michibayashi, K.; de Obeso, J. C.; D'Andres, J.; Lefay, R.; Leong, J. A. M.; Zeko, D.; Kelemen, P. B.; Teagle, D. A. H.

2017-12-01

Oman Drilling Project Hole GT3A intersected 400 m of altered basaltic dikes, gabbros, and diorites. The 100% recovery affords an unprecedented opportunity to study metamorphism and hydrothermal alteration near the dike-gabbro transition in the ocean crust. Hydrothermal alteration is ubiquitous; all rocks are at least moderately altered, and mean alteration intensity is 54%. The earliest alteration in all rock types is background replacement of igneous minerals, some of which occurred at clinopyroxene amphibolite facies, as indicated by brown-green hornblende, calcic plagioclase, and secondary cpx. In addition, background alteration includes greenschist, subgreenschist, and zeolite facies minerals. More extensive alteration is locally observed in halos around veins, patches, and zones related to deformation. Dense networks of hydrothermal veins record a complex history of fluid-rock alteration. During core description, 10,727 individual veins and 371 vein networks were logged in the 400 m of Hole GT3A. The veins displayed a range of textures and connectivities. The total density of veins in Hole GT3A is 26.8 veins m-1. Vein density shows no correlation with depth, but may be higher near dike margins and faults. Vein minerals include amphibole, epidote, quartz, chlorite, prehnite, zeolite (chiefly laumontite) and calcite in a range of combinations. Analysis of crosscutting relations leads to classification of 4 main vein types. In order of generally oldest to youngest these are: amphibole, quartz-epidote-chlorite (QEC), zeolite-prehnite (ZP), and calcite. QEC and ZP vein types may contain any combination of minerals except quartz alone; veins filled only by quartz may occur at any relative time. Macroscopic amphibole veins are rare and show no variation with depth. QEC vein densities appear to be higher (>9.3 veins m-1) in the upper 300 m of GT3A, where dikes predominate. In contrast, there are 5.5 veins m-1 at 300-400 m, where gabbros and diorites are abundant. ZP veins increase in density downhole; the highest density of 17.5 ZP veins/m occurs in the lowest 100 m where substantial faulting is observed. Equilibrium coexistence of laumontite and prehnite in ZP veins implies formation at 100-250 °C, lower than amphibole and QEC veins. Calcite veins are abundant only in the uppermost 100 m of the hole.

Hydrothermal Alteration of the Lower Oceanic Crust: Insight from OmanDP Holes GT1A and GT2A.

NASA Astrophysics Data System (ADS)

Harris, M.; Zihlmann, B.; Mock, D.; Akitou, T.; Teagle, D. A. H.; Kondo, K.; Deans, J. R.; Crispini, L.; Takazawa, E.; Coggon, J. A.; Kelemen, P. B.

2017-12-01

Hydrothermal circulation is a fundamental Earth process that is responsible for the cooling of newly formed ocean crust at mid ocean ridges and imparts a chemical signature on both the crust and the oceans. Despite decades of study, the critical samples necessary to resolve the role of hydrothermal circulation during the formation of the lower ocean crust have remained poorly sampled in the ocean basins. The Oman Drilling Project successfully cored 3 boreholes into the lower crust of the Semail ophiolite (Holes GT1A layered gabbros, GT2A foliated gabbros and GT3A dike/gabbro transition). These boreholes have exceptionally high recovery ( 100%) compared to rotary coring in the oceans and provide an unrivalled opportunity to quantitatively characterise the hydrothermal system in the lower oceanic crust. Hydrothermal alteration in Holes GT1A and GT2A is ubiquitous and manifests as secondary minerals replacing primary igneous phases and secondary minerals precipitated in hydrothermal veins and hydrothermal fault zones. Hole GT1A is characterised by total alteration intensities between 10 -100%, with a mean alteration intensity of 60%, and shows no overall trend downhole. However, there are discrete depth intervals (on the scale of 30 -100 m) where the total alteration intensity increases with depth. Alteration assemblages are dominated by chlorite + albite + amphibole, with variable abundances of epidote, clinozoisite and quartz. Hole GT1A intersected several hydrothermal fault zones, these range from 2-3 cm up to >1m in size and are associated with more complex secondary mineral assemblages. Hydrothermal veins are abundant throughout Hole GT1A, with a mean density of 37 vein/m. Hole GT2A is characterised by total alteration intensities between 6-100%, with a mean alteration intensity of 45%, and is highly variable downhole. Alteration halos and patches are slightly more abundant than in Hole GT1A. The secondary mineral assemblage is similar to Hole GT1A, but Hole GT2A has higher abundances of epidote, clinozoisite, quartz, laumontite and iron-oxydroxides. Vein density in Hole GT2A is 61 veins/m. In both holes, cross cutting vein relationships indicate a relative timing from earliest to latest of: amphibole; epidote + zoisite + qtz; chlorite + prehnite + qtz, calcite-laumontite-anhydrite; gypsum.

Thermal Expansivity Between 150 and 800°C of Hydrothermally Altered Conduit Dyke Samples from USDP-4 Drill Core (Mt Unzen, Shimabara, Japan)

NASA Astrophysics Data System (ADS)

Yilmaz, T. I.; Hess, K. U.; Vasseur, J.; Wadsworth, F. B.; Gilg, H. A.; Nakada, S.; Dingwell, D. B.

2017-12-01

When hot magma intrudes the crust, the surrounding rocks expand. Similarly, the cooling magma contracts. The expansion and contraction of these multiphase materials is not simple and often requires empirical constraint. Therefore, we constrained the thermal expansivity of Unzen dome and conduit samples using a NETZSCH® DIL 402C. Following experiments, those samples were scanned using a Phoenix v|tome|x m to observe the cracks that may have developed during the heating and cooling. The dome samples do not show petrological or chemical signs of alteration. However, the alteration of the conduit dykes is represented by the occurrence of the main secondary phases such as chlorite, sulfides, carbonates, R1 (Reichweite parameter) illite-smectite, and kaolinite. These alteration products indicate an (I) early weak to moderate argillic magmatic alteration, and a (II) second stage weak to moderate propylitic hydrothermal alteration. The linear thermal expansion coefficient aL of the dome material is K-1 between 150° and 800°C and shows a sharp peak of up to K-1 around the alpha-beta-quartz-transition ( 573°C). In contrast, aL of the hydrothermally altered conduit samples starts to increase around 180° and reaches K-1 at 400°C. We interpret this effect as being due to the water content of the kaolinite and the R1 illite-smectite, which induces larger expansions per degree temperature change. Furthermore, the altered conduit samples show a more pronounced increases of aL between 500 and 650°C of up to peaks at K-1, which is generated by the breakdown of chlorite, iron-rich dolomite solid solutions, calcite, and pyrite. We use a 1D conductive model of heat transfer to explore how the country rock around the Unzen conduit zone would heat up after intrusion. In turn, we convert these temperature profiles to thermal stress profiles, assuming the edifice is largely undeformable. We show that these high linear thermal expansion coefficients of the hydrothermally altered conduit rocks may large induce thermal stresses in the surrounding host rock and therefore promotes cracking, which may in turn lead to edifice instability.

Dismantling processes of basaltic shield volcanoes - origin of the Piton des Neiges breccias - Reunion Island

NASA Astrophysics Data System (ADS)

Arnaud, A.; Bachèlery, B.; Cruchet, C.

2003-04-01

Reunion Island is mainly composed by two volcanic massifs: the active Piton de la Fournaise to the southeast and the Piton des Neiges to the northwest that has been inactive for about 12000 years. The latter corresponds to a dismantled volcanic massif, deeply cut by valleys and by three vast depressions, called “cirques” around the centre of the volcano. They offer the opportunity to observe the inside of a basaltic shield volcano. The first work dealing with the origin of the “cirques” very quickly showed the existence of a significant cover of breccia deposits. These breccias were often interpreted as the result of a major stage of erosion considered as partly at the origin of the “cirques” formation. Geological campaigns mainly achieved in the “cirque de Salazie” (eastern of the Piton des Neiges), allow to establish a first typology based on morphological, phenomenological and sedimentary features of the deposits. Two main complexes of breccias have been distinguished. An old complex outcropping in the internal parts of the cirque and an upper complex generally overlaying the lower complex. The old complex comprises two main units of breccias. These units show a strong alteration marked by the presence of clays, chlorites, serpentines and zeolites. In the inner part of the cirque, these breccias are closely related to the old lava formations from which they come. These units show frequent jigsaw-cracks, a chaotic stratigraphy, as well as large amounts of chlorite. The upper complex is constituted by four main units which are more or less geographically separated in the cirque of Salazie. Their limits are not yet well identified because of the significant relief and a strong vegetable cover. Several units display a very strong fracturation, jigsaw-cracks and a chaotic stratigraphy whereas many lava flows are pulverised and locally injected in scoria levels. Recent work on Saint-Gilles breccias (Fèvre et al., this meeting) allowed to identify several sub-aerials deposits of debris avalanches. These new data, the analysis of geology and sedimentary figures observed within the breccia units in the “cirque de Salazie”, evidence several major gravitational collapse affecting the northeast flank of Piton des Neiges volcano. Considering that, the “cirque de Salazie” appears as partly bounded by gravitational collapse affecting the flanks of the volcano.

Modification of the magnetic mineralogy in basalts due to fluid-rock interactions in a high-temperature geothermal system (Krafla, Iceland)

NASA Astrophysics Data System (ADS)

Oliva-Urcia, Belén; Kontny, Agnes; Vahle, Carsten; Schleicher, Anja M.

2011-07-01

Active high-temperature (>150 °C) geothermal areas like the Krafla caldera, NE-Iceland, often show distinct magnetic lows in aeromagnetic anomaly maps suggesting a destruction of magnetic minerals by hydrothermal activity. The main alteration processes in such an environment are low-temperature oxidation (<350 °C, maghemitization) and fluid-rock interactions. We investigated the rock magnetic properties [natural remanent magnetization (NRM) magnetic susceptibility and their temperature and field variation] and the mineralogy, using X-ray diffraction, microscopic methods and electron microprobe analyses, of two drill cores (KH1 and KH3) from the rim of the Krafla caldera. The drill cores have distinctly lower NRM values (average <3 A m-1) compared to younger surface basalts (average 20 A m-1) along with a large variation in magnetic susceptibility (1.3 × 10-7- 4.9 × 10-5 m3 kg-1). The secondary mineral assemblage (sulphides, sphene, rutile and chlorite) indicates an alteration within the chlorite-smectite zone for both cores without depth zoning. Optical miscroscopy in combination with the Bitter technique and backscatter electron microscopy along with the thermomagnetic analyses allow distinguishing two different magnetomineralogical groups of titanomaghemite: (1) titanomaghemite with intermediate titanium concentration and probably high vacancy concentration, and (2) titanomaghemite with low titanium concentration and low vacancy concentration. The mineral assemblages, textures and magnetic properties deduced from the mentioned magnetic measurements indicate two-stage transformation mechanism: (1) Dissolution of titanium at low pH under oxidizing conditions. The ulvöspinel component of titanomagnetite and ilmenite forms rutile or sphene, and Fe2 + migrates out of the spinel lattice forming titanomaghemite. (2) Formation of pyrite and dissolution of remaining titanomaghemite under reducing and acidic conditions. The latter mechanism produces ghost textures (all titanomaghemite is transformed and only their former grain shapes are preserved), with only paramagnetic minerals left and ferrimagnetic minerals nearly dissolved. This mechanism could explain the significant magnetization loss, which is seen in many local magnetic anomaly lows within the oceanic crust and volcanic islands like Iceland or Hawaii. The production of nanoporous textures in titanomaghemites is suggested as a mechanism for the enhancement of the magnetic susceptibility values related to the hydrothermal alteration of Krafla.

Isotopic exchange in mineral-fluid systems. IV. The crystal chemical controls on oxygen isotope exchange rates in carbonate-H 2O and layer silicate-H 2O systems

NASA Astrophysics Data System (ADS)

Cole, David R.

2000-03-01

Oxygen isotope exchange between minerals and water in systems far from chemical equilibrium is controlled largely by surface reactions such as dissolution-precipitation. In many cases, this behavior can be modeled adequately by a simple pseudo-first order rate model that accounts for changes in surface area of the solid. Previous modeling of high temperature isotope exchange data for carbonates, sulfates, and silicates indicated that within a given mineral group there appears to be a systematic relationship between rate and mineral chemistry. We tested this idea by conducting oxygen isotope exchange experiments in the systems, carbonate-H 2O and layer silicate-H 2O at 300 and 350°C, respectively. Witherite (BaCO 3), strontianite (SrCO 3) and calcite (CaCO 3) were reacted with pure H 2O for different lengths of time (271-1390 h) at 300°C and 100 bars. The layer silicates, chlorite, biotite and muscovite were reacted with H 2O for durations ranging from 132 to 3282 h at 350°C and 250 bars. A detailed survey of grain sizes and grain habits using scanning electron microscopy (SEM) indicated that grain regrowth occurred in all experiments to varying extents. Changes in the mean grain diameters were particularly significant in experiments involving withertite, strontianite and biotite. The variations in the extent of oxygen isotope exchange were measured as a function of time, and fit to a pseudo-first order rate model that accounted for the change in surface area of the solid during reaction. The isotopic rates (ln r) for the carbonate-H 2O system are -20.75 ± 0.44, -18.95 ± 0.62 and -18.51 ± 0.48 mol O m -2 s -1 for calcite, strontianite and witherite, respectively. The oxygen isotope exchange rates for layer silicate-H 2O systems are -23.99 ± 0.89, -23.14 ± 0.74 and -22.40 ± 0.66 mol O m -2 s -1 for muscovite, biotite and chlorite, respectively. The rates for the carbonate-H 2O systems increase in order from calcite to strontianite to witherite. This order clearly reflects the influence of the change in cation chemistry, i.e., Ba > Sr > Ca. A similar pattern is observed for the layer silicate-H 2O systems, where chlorite>biotite>muscovite. The link between cation chemistry and rate is more complicated in this case, but in general, the order follows a trend where Mg-Fe > K-Mg > K, with an associated increase in Si and Al, and decrease in hydroxyl. The isotopic-chemical relations suggest that oxygen isotope exchange behavior monitored experimentally in this study is the net result of bond-breaking and dissolution of the mineral, complex ion formation in solution and growth of the mineral, whose structure is controlled, in large part, by the lattice energy. We compared the rates against the electrostatic attractive lattice energies (neglecting the repulsive forces), normalized per number of cations. The correlations between rates and lattice energies are quite good for both mineral-H 2O systems. The increase in rates correlated with a decrease in the electrostatic attractive lattice energies, i.e., the greater the lattice energy required to break up the crystal, the more sluggish the rates for both chemical and isotopic exchange. By establishing an unambiguous relationship between rate, lattice energy, and ultimately temperature, we can begin to develop empirical equations useful in predicting rates of isotopic exchange for minerals for which experimental data are lacking.

Cataclastic rocks of the San Gabriel fault—an expression of deformation at deeper crustal levels in the San Andreas fault zone

NASA Astrophysics Data System (ADS)

Anderson, J. Lawford; Osborne, Robert H.; Palmer, Donald F.

1983-10-01

The San Gabriel fault, a deeply eroded late Oligocene to middle Pliocene precursor to the San Andreas, was chosen for petrologic study to provide information regarding intrafault material representative of deeper crustal levels. Cataclastic rocks exposed along the present trace of the San Andreas in this area are exclusively a variety of fault gouge that is essentially a rock flour with a quartz, feldspar, biotite, chlorite, amphibole, epidote, and Fe-Ti oxide mineralogy representing the milled-down equivalent of the original rock (Anderson and Osborne, 1979; Anderson et al., 1980). Likewise, fault gouge and associated breccia are common along the San Gabriel fault, but only where the zone of cataclasis is several tens of meters wide. At several localities, the zone is extremely narrow (several centimeters), and the cataclastic rock type is cataclasite, a dark, aphanitic, and highly comminuted and indurated rock. The cataclastic rocks along the San Gabriel fault exhibit more comminution than that observed for gouge along the San Andreas. The average grain diameter for the San Andreas gouge ranges from 0.01 to 0.06 mm. For the San Gabriel cataclastic rocks, it ranges from 0.0001 to 0.007 mm. Whereas the San Andreas gouge remains particulate to the smallest grain-size, the ultra-fine grain matrix of the San Gabriel cataclasite is composed of a mosaic of equidimensional, interlocking grains. The cataclastic rocks along the San Gabriel fault also show more mineralogiec changes compared to gouge from the San Andreas fault. At the expense of biotite, amphibole, and feldspar, there is some growth of new albite, chlorite, sericite, laumontite, analcime, mordenite (?), and calcite. The highest grade of metamorphism is laumontite-chlorite zone (zeolite facies). Mineral assemblages and constrained uplift rates allow temperature and depth estimates of 200 ± 30° C and 2-5 km, thus suggesting an approximate geothermal gradient of ~50°C/km. Such elevated temperatures imply a moderate to high stress regime for the San Andreas, which is consistent with experimental rock failure studies. Moreover, these results suggest that the previously observed lack of heat flow coaxial with the fault zone may be the result of dissipation rather than low stress. Much of the mineralogy of the cataclastic rocks is still relict from the earlier igneous or metamorphic history of the protolith; porphyroclasts, even in the most deformed rocks, consist of relict plagioclase (oligoclase to andesine), alkali feldspar, quartz, biotite, amphibole, epidote, allanite, and Fe-Ti oxides (ilmenite and magnetite). We have found no significant development of any clay minerals (illite, kaolinite, or montmorillonite). For many sites, the compositions of these minerals directly correspond to the mineral compositions in rock types on one or both sides of the fault. Whole rock major and trace element chemistry coupled with mineral compositions show that mixing within the zone of cataclasis is not uniform, and that originally micaceous foliated, or physically more heterogeneous rock units may contribute a disproportionally large amount to the resultant intrafault material. As previously found for the gouge along the San Andreas, chemical mobility is not a major factor in the formation of cataclastic rocks of the San Gabriel fault. We see only minor changes for Si and alkalies; however, there is a marked mobility of Li, which is a probable result of the alteration and formation of new mica minerals. The gouge of the San Andreas and San Gabriel faults probably formed by cataclastic flow. There is some indication, presently not well constrained, that the fine-grained matrix of the cataclasite of from the San Gabriel fault formed in response to superplastic flow.

Mineralogy of metasomatic rocks and geochronology of the Olhovka porphyry-copper deposit, Chukotka, Russia

NASA Astrophysics Data System (ADS)

Rogacheva, Lyuba; Baksheev, Ivan

2010-05-01

The Olkhovka porphyry-copper deposit located on the border of foreland of the Okhotsk-Chukotka volcanic belt (OCVB) and a ledge composed of the Late Jurassic-Early Cretaceous Uda-Murgal arc (J3-K1) rocks is hosted by monzonite stock attributed to the Upper Cretaceous Kavralyan complex - K2) We estimated age of the Olkhovka monzonite by Rb-Sr and U-Pb methods. Rb-Sr age was determine om the basis of isotopic analysis of 8 monomineralic samples (potassium feldspar, plagioclase, amphibole, and dark mica). Isochron constructed on the basis of Rb-Sr data corresponds to the age of 78 + 2.6 Ma (MSWD=0.23). The Rb-Sr age is supported by U-Pb data derived from zircon of the same rock. One hundred and three single crystals of zircon were analyzed. Uranium content ranges from 52.66 ppm to 579.64 ppm; U/Th isotopic ratio varies from 0.567 to 1.746; age is 78.02+0.65 Ma (MSWD = 2.8). Monzonite is propylitized in variable degree. Propylite is composed of actinolite, chlorite, albite, quartz, and calcite. Propylite are cut by quartz-tourmaline veins. In addition, quartz-tourmaline metasomatic rock was identified in rhyolite ignimbrite out of the stock. Microscopically, tourmaline crystals of both types are oscilatory zoned that is caused by variable Fe content. Tourmalines of both assemblages can be classified as intermediate member of the schorl ("oxy-schorl")-dravite ("oxy-dravite") series. The Fetot/ (Fetot+Mg) varies from 0.31 to 0.95 in propylitic tourmaline and from 0.11 to 0.49, in quartz-tourmaline altered rocks from ignimbrite. Despite similar composition of both tourmalines, the major isomorphic substitutions in them are different. In propylite tourmaline, it is Fe → Al, whereas in the second case, it is Fe → Mg with certain effect of the Fe → Al type. Fe → Al isomorphic substitution is typical of porphyry style deposits (Baksheev et al., 2009 [1]). Therefore, we can conclude that quartz-tourmaline alteration in ignimbrite does not related to the formation of the deposit. Chlorite from propylitized monzonite occurs as flakes up to few hundred microns in size. The mineral is associated with muscovite and actinolite. The Fetot/ (Fetot+Mg) ratio ranges from 0.27 to 0.46 that allowing attribution this chlorite to Fe-rich clinochlore. White mica studied here belongs to muscovite ( 3.04-3.33 apfu Si). Amphiboles evolved from primary magnesihorblende (6.86 apfu Si, 0.48 apfu Na, 1.72 apfu Ca, Mg# 0.71) through early metasomatic actinolite hornblende (7.54 apfu Si, 0.18 apfu Na, 1.81 apfu Ca, Mg# 0.71) to late metasomatic actinolite (7.76 apfu Si, 0.07 apfu Na, 1.74 apfu Ca, Mg# 0.69). Thus, we obtained first data on age of monzonite stock, which hosts porphyry-copper deposit. Monzonite is of rather young age probably corresponding to the final stage of the OCVB evolution (Tikhomirov et al., 2006 [2]), . Mineralogy and chemical composition of minerals from propylite were studied. In general chemical data are consistent with those from other porphyry-copper deposits. References: [1] Baksheev I.A, TikhomirovP.L., Yapaskurt, V.O., Vigasina M.F., Prokofev V.Yu.&. Ustinov V.I. (2009): Tourmaline of the Mramorny tin cluster, Chukotka Peninsula, Russia. Canad. Mineral. 47 (5), 1177-1194. [2] P.L Tikhomirov, V.V. Akinin V.O. Ispolatov P. Alexsandr et al. Age of north part of OCVB: New Ar-Ar and U-Pb geochronology data. (2006) Stratigrafiya. Geologicheskaya korrelyatsiya.14. 5. 81-95 in russian.

Prograde and retrograde metamorphic processes in high-pressure subduction zone serpentinites from East Thessaly, Greece

NASA Astrophysics Data System (ADS)

Koutsovitis, Petros

2016-04-01

The East Thessaly region, Central Greece, includes metaophiolitic mélange formations which extend from the eastern foothills of Mt. Olympus and Ossa, throughout the Agia basin, Mt. Mavrovouni (Sklithro region), South Pelion and reaching up to northeast Othris (regions of Aerino and Velestino). They appear in the form of dispersed and deformed thrust sheets having been variably emplaced onto Mesozoic platform series rocks of the Pelagonian tectonostratigraphic zone[1]. These formations consist mainly of serpentinites, as well as metasediments, metagabbros, metadolerites, rodingites, ophicalcites, talc-schists and chromitites. Based upon petrographic observations, mineral chemistry data and XRD patterns, the subduction zone-related serpentinites from the regions of Potamia, Anavra, Aetolofos and Kalochori-Chasanbali (Agia basin), as well as from the regions of Aerino and Velestino, are characterized by the progressive transformation of lizardite to antigorite and are distinguished into two groups. The first group includes serpentinites from the metaophiolitic formations of Potamia, Anavra, Aerino and Velestino, which are marked by destibillization of lizardite to antigorite, mostly along the grain boundaries of the lizardite mesh textured relics. The presence of lizardite and antigorite in almost equal amounts indicates medium-temperature blueschist facies metamorphic conditions (˜340-370 ° C; P≈10-11 kbar)[2,3,4]. The second serpentinite group appears in the regions of Aetolofos and Kalochori, characterized by the predominance of antigorite, the minor occurrence of lizardite and the complete replacement of spinel by Cr-magnetite. The absence of metamorphic olivine suggests that these serpentinites were most likely formed at slightly higher temperature and pressure conditions compared to the first serpentinite group, corresponding to medium or high temperature blueschist facies metamorphism (˜360-380 ° C; P≈12 kbar)[2,3,4]. These metamorphic conditions are highly comparable with the P-T estimates from the East Thessaly metabasic rocks (˜350 ° C; P≈10-11 kbars)[5], suggesting that the entire metaophiolitic formation underwent blueschist facies metamorphism, comparable with high-pressure metaophiolitic formations appearing in Evia, Attica and the Cyclades. The East Thessaly serpentinites exhibit significantly high PM-normalized Pb, U enrichments and rather high Cs, La, As and Sb concentrations, which are comparable with subduction-related serpentinites, formed after mantle wedge peridotite hydration, and that have interacted with sedimentary derived fluids [2,6,7,8]. These serpentinites were also partly affected by de-serpentinization retrograde metamorphism (estimated at P<8 kbar and T<350 ° C) which is noticed by the following: secondary crosscuting antigorite veins occasionally with chlorite, coronas of chlorite along Cr-magnetite crystals, appearance of secondary calcite veins and talc. In the Kalochori-Chasanbali area, intense carbonization processes formed ophicalcite breccias enveloped by imbricated serpentinites[9], whereas talc-rich serpentinites appear in the region of Sklithro. Retrograde metamorphism may have occurred during exhumation, possibly within a serpentinite channel[8]. In addition, their retrograde history can also be indirectly identified through the study of their rodingite intrusions and more specifically through the formation of late-stage vesuvianite-rich dykes at low-moderate temperature conditions (T=250-300 oC) and subsequent derodingitization processes, forming metarodingites. The latter include abundant high-Mg replacive chlorite formed by continuous serpentinization which provided Mg2+ to the infiltrating fluids, causing the partial breakdown of Ca-bearing minerals. References. [1] Pe-Piper & Piper 2002: Borntraeger, Stuttgart, 1-645; [2] Lafay et al 2013: Chem Geol 343, 38-54; [3] Schwartz et al 2013: Lithos 178, 197-210; [4] Guillot, et al 2015: Tectonophysics 646, 1-19; [5] Perraki et al 2002: Geologica Carpathica 53, 164-165; [6] Deschamps, et al 2013: Lithos 178, 96-127; [7] Hattori & Guillot, 2007: G-Cubed 8 (9); [8] Barnes et al 2014: Chemi Geol 389, 29-47; [9] Melfos et al 2009: Geoph. Res. Abst, 11.

High resolution remote sensing information identification for characterizing uranium mineralization setting in Namibia

NASA Astrophysics Data System (ADS)

Zhang, Jie-Lin; Wang, Jun-hu; Zhou, Mi; Huang, Yan-ju; Xuan, Yan-xiu; Wu, Ding

2011-11-01

The modern Earth Observation System (EOS) technology takes important role in the uranium geological exploration, and high resolution remote sensing as one of key parts of EOS is vital to characterize spectral and spatial information of uranium mineralization factors. Utilizing satellite high spatial resolution and hyperspectral remote sensing data (QuickBird, Radarsat2, ASTER), field spectral measurement (ASD data) and geological survey, this paper established the spectral identification characteristics of uranium mineralization factors including six different types of alaskite, lower and upper marble of Rössing formation, dolerite, alkali metasomatism, hematization and chloritization in the central zone of Damara Orogen, Namibia. Moreover, adopted the texture information identification technology, the geographical distribution zones of ore-controlling faults and boundaries between the different strata were delineated. Based on above approaches, the remote sensing geological anomaly information and image interpretation signs of uranium mineralization factors were extracted, the metallogenic conditions were evaluated, and the prospective areas have been predicted.

Mineralogy of mine waste at the Vermont Asbestos Group mine, Belvidere Mountain, Vermont

USGS Publications Warehouse

Levitan, D.M.; Hammarstrom, J.M.; Gunter, M.E.; Seal, R.R.; Chou, I.-Ming; Piatak, N.M.

2009-01-01

Samples from the surfaces of waste piles at the Vermont Asbestos Group mine in northern Vermont were studied to determine their mineralogy, particularly the presence and morphology of amphiboles. Analyses included powder X-ray diffraction (XRD), optical microscopy, scanning electron microscopy (SEM), electron probe microanalysis (EPMA), and Raman spectroscopy. Minerals identified by XRD were serpentine-group minerals, magnetite, chlorite, quartz, olivine, pyroxene, and brucite; locally, mica and carbonates were also present. Raman spectroscopy distinguished antigorite and chrysotile, which could not be differentiated using XRD. Long-count, short-range XRD scans of the (110) amphibole peak showed trace amounts of amphibole in most samples. Examination of amphiboles in tailings by optical microscopy, SEM, and EPMA revealed non-fibrous amphiboles compositionally classified as edenite, magnesiohornblende, magnesiokatophorite, and pargasite. No fibrous amphibole was found in the tailings, although fibrous tremolite was identified in a sample of host rock. Knowledge of the mineralogy at the site may lead to better understanding of potential implications for human health and aid in designing a remediation plan.

Caractérisation des paragenèses et des paléocirculations fluides dans l'indice d'or de Bleïda (Anti-Atlas, Maroc)Characterization of the paragenesis and the fluid palaeo-circulations in the gold showings of Bleida (Anti-Atlas, Morocco)

NASA Astrophysics Data System (ADS)

Barakat, Ahmed; Marignac, Christian; Boiron, Marie-Christine; Bouabdelli, Mohamed

2002-01-01

The gold showings at Bleida are hosted in Late Pan-African N50-80 °E quartz-hematite-chlorite 1 tension lenses that are related to the activity of major sinistral sub-east-west thrusts. Ores result from three superimposed stages of fluid migration. Gold occurs in microcracks offsetting the earlier minerals. Fluids evolved from COHN compositions with a saline component to boiling aqueous fluids. Pressure and temperature decreased from 50 MPa and 300 °C to less than 4 MPa and 150 °C. Thus, the gold showings at Bleida were formed in a typical geothermal (epithermal) setting, likely controlled by the Late Pan-African magmatism. To cite this article: A. Barakat et al., C. R. Geoscience 334 (2002) 35-41

Apports des phyllosilicates dans la différenciation entre altération hypogène et altération supergène dans le basalte triasique du Moyen Atlas (Maroc)Contribution of phyllosilicates to distinguish between hypogene alteration and weathering in Triassic basalt from Middle Atlas (Morocco)

NASA Astrophysics Data System (ADS)

Dekayir, Abdelilah; Danot, Michel; Allali, Nabil

2002-09-01

Triassic basalt of the Middle Atlas has been subject to metamorphic transformation then weathering. Occurrence in both metabasalt and saprolite of ubiquitous clay minerals, such as smectite and mixed layers chlorite-smectite, makes it difficult to distinguish between the two alteration facies and explains the interest of complementary sources of information. In the Bhallil weathering profile, petrographical and mineralogical analyses of primary igneous minerals and their alteration products coupled with Fe oxidation state determination in clay fractions allow to identify three alteration facies: ( i) metamorphic basalt, where iron occurs mainly as the ferrous form; ( ii) the lower part of saprolite, where iron is partially oxidized to its ferric form; ( iii) the upper part of saprolite, where iron is completely oxidized. To cite this article: A. Dekayir et al., C. R. Geoscience 334 (2002) 877-884.

Characterization of alkyl carbon in forest soils by CPMAS 13C NMR spectroscopy and dipolar dephasing

USGS Publications Warehouse

Kogel-Knabner, I.; Hatcher, P.G.

1989-01-01

Samples obtained from forest soils at different stages of decomposition were treated sequentially with chloroform/methanol (extraction of lipids), sulfuric acid (hydrolysis), and sodium chlorite (delignification) to enrich them in refractory alkyl carbon. As revealed by NMR spectroscopy, this treatment yielded residues with high contents of alkyl carbon. In the NMR spectra of residues obtained from litter samples, resonances for carbohydrates are also present, indicating that these carbohydrates are tightly bound to the alkyl carbon structures. During decomposition in the soils this resistant carbohydrate fraction is lost almost completely. In the litter samples the alkyl carbon shows a dipolar dephasing behavior indicative of two structural components, a rigid and a more mobile component. As depth and decomposition increase, only the rigid component is observed. This fact could be due to selective degradation of the mobile component or to changes in molecular mobility during decomposition, e.g., because of an increase in cross linking or contact with the mineral matter of the soil.

Degradation of carbohydrates during dilute sulfuric acid pretreatment can interfere with lignin measurements in solid residues.

PubMed

Katahira, Rui; Sluiter, Justin B; Schell, Daniel J; Davis, Mark F

2013-04-03

The lignin content measured after dilute sulfuric acid pretreatment of corn stover indicates more lignin than could be accounted for on the basis of the untreated corn stover lignin content. This phenomenon was investigated using a combination of (13)C cross-polarization/magic-angle spinning (CP/MAS) solid-state nuclear magnetic resonance (NMR) spectroscopy and lignin removal using acid chlorite bleaching. Only minimal contamination with carbohydrates and proteins was observed in the pretreated corn stover. Incorporating degradation products from sugars was also investigated using (13)C-labeled sugars. The results indicate that sugar degradation products are present in the pretreatment residue and may be intimately associated with the lignin. Studies comparing whole corn stover (CS) to extractives-free corn stover [CS(Ext)] clearly demonstrated that extractives are a key contributor to the high-lignin mass balance closure (MBC). Sugars and other low molecular weight compounds present in plant extractives polymerize and form solids during pretreatment, resulting in apparent Klason lignin measurements that are biased high.

Preliminary report on the clay mineralogy of the Upper Devonian Shales in the southern and middle Appalachian Basin

USGS Publications Warehouse

Hosterman, John W.; Loferski, Patricia J.

1978-01-01

The distribution of kaolinite in parts of the Devonian shale section is the most significant finding of this work. These shales are composed predominately of 2M illite and illitic mixed-layer clay with minor amounts of chlorite and kaolinite. Preliminary data indicate that kaolinite, the only allogenic clay mineral, is present in successively older beds of the Ohio Shale from south to north in the southern and middle parts of the Appalachian basin. This trend in the distribution of kaolinite shows a paleocurrent direction to the southwest. Three well-known methods of preparing the clay fraction for X-ray diffraction analysis were tested and evaluated. Kaolinite was not identified in two of the methods because of layering due to differing settling rates of the clay minerals. It is suggested that if one of the two settling methods of sample preparation is used, the clay film be thin enough for the X-ray beam to penetrate the entire thickness of clay.

Geological sources of fluoride and acceptable intake of fluoride in an endemic fluorosis area, southern Iran.

PubMed

Battaleb-Looie, Sedigheh; Moore, Farid; Jacks, Gunnar; Ketabdari, Mohammad Reza

2012-10-01

The present study is the first attempt to put forward possible source(s) of fluoride in the Dashtestan area, Bushehr Province, southern Iran. In response to reports on the high incidence of dental fluorosis, 35 surface and groundwater samples were collected and analysed for fluoride. The results indicate that dissolved fluoride in the study area is above the maximum permissible limit recommended by the World Health Organization (WHO). An additional 35 soil and rock samples were also collected and analysed for fluoride, and rock samples were subjected to petrographic investigations and X-ray diffraction. The results of these analyses show that the most likely source for fluoride in the groundwater is from clay minerals (chlorite) and micas (muscovite, sericite, and biotite) in the soils and rocks in the area. We also note that due to the high average temperatures all year round and excessive water consumption in the area, the optimum fluoride dose level should be lower than that recommended by the WHO.

Online characterization of planetary surfaces: PlanetServer, an open-source analysis and visualization tool

NASA Astrophysics Data System (ADS)

Marco Figuera, R.; Pham Huu, B.; Rossi, A. P.; Minin, M.; Flahaut, J.; Halder, A.

2018-01-01

The lack of open-source tools for hyperspectral data visualization and analysis creates a demand for new tools. In this paper we present the new PlanetServer, a set of tools comprising a web Geographic Information System (GIS) and a recently developed Python Application Programming Interface (API) capable of visualizing and analyzing a wide variety of hyperspectral data from different planetary bodies. Current WebGIS open-source tools are evaluated in order to give an overview and contextualize how PlanetServer can help in this matters. The web client is thoroughly described as well as the datasets available in PlanetServer. Also, the Python API is described and exposed the reason of its development. Two different examples of mineral characterization of different hydrosilicates such as chlorites, prehnites and kaolinites in the Nili Fossae area on Mars are presented. As the obtained results show positive outcome in hyperspectral analysis and visualization compared to previous literature, we suggest using the PlanetServer approach for such investigations.

Methods for enhancing mapping of thermal fronts in oil recovery

DOEpatents

Lee, D.O.; Montoya, P.C.; Wayland, J.R. Jr.

1984-03-30

A method for enhancing the resistivity contrasts of a thermal front in an oil recovery production field as measured by the controlled source audio frequency magnetotelluric (CSAMT) technique is disclosed. This method includes the steps of: (1) preparing a CSAMT-determined topological resistivity map of the production field; (2) introducing a solution of a dopant material into the production field at a concentration effective to alter the resistivity associated with the thermal front; said dopant material having a high cation exchange capacity which might be selected from the group consisting of montmorillonite, illite, and chlorite clays; said material being soluble in the conate water of the production field; (3) preparing a CSAMT-determined topological resistivity map of the production field while said dopant material is moving therethrough; and (4) mathematically comparing the maps from step (1) and step (3) to determine the location of the thermal front. This method is effective with the steam flood, fire flood and water flood techniques.

Mineral resource assessment of the Dillon 1 degree x 2 degrees Quadrangle, Idaho and Montana

USGS Publications Warehouse

Pearson, Robert Carl; Trautwein, C.M.; Ruppel, E.T.; Hanna, W.F.; Rowan, L.C.; Loen, J.S.; Berger, B.R.

1992-01-01

The Dillon 1°x2° quadrangle in southwestern Montana and east-central Idaho was investigated as part of the U.S. Geological Survey's Conterminous United States Mineral Assessment Program (CUSMAP) to determine its mineral resource potential. An interdisciplinary study was made of geology, geochemistry, geophysics (gravity and aeromagnetics), remote sensing, and mineral deposits. The results of those studies, as well as mineral resource assessment of numerous mineraldeposit types, are published separately as a folio of maps. This report summarizes the studies, provides background information on them, and presents a selected bibliography relevant to the geology and mineral resources of the quadrangle. The quadrangle contains large resources of gold and substantial resources of talc and chlorite, all of which were being mined in the 1980's and early 1990's. Submarginal resources of molybdenum, copper, tungsten, and iron range from moderately large to large. Other commodities that may be present in significant amounts are chromite, lead, zinc, silver, barite, zeolite minerals, and various nonmetallic metamorphic minerals.

Petrology, composition, and age of intrusive rocks associated with the Quartz Hill molybdenite deposit, southeastern Alaska.

USGS Publications Warehouse

Hudson, T.; Smith, James G.; Elliott, R.L.

1979-01-01

A large porphyry molybdenum deposit (Quartz Hill deposit) was recently discovered in the heart of the Coast Range batholithic complex about 70 km E of Ketchikan, SE Alaska. Intrusive rocks associated with the mineral deposit form two composite epizonal to hypabyssal stocks and many dikes in country rocks. All observed metallization and alteration is within the Quartz Hill stock. Molybdenite forms fracture coatings and occurs in veins with quartz. Alteration is widespread and includes development of secondary quartz, pyrite, K-feldspar, biotite, white mica, chlorite, and zeolite. Field relations indicate that the stocks were emplaced after regional uplift and erosion of the Coast Range batholithic complex, and K-Ar data show that intrusion and alteration took place in late Oligocene time, about 27 to 30 Ma ago. Data from the Ketchikan quadrangle indicate that porphyry molybdenum metallization in the Coast Range batholithic complex is associated with regionally extensive but spotty, middle Tertiary or younger, felsic magmatism. -from Authors

Widespread abiotic methane in chromitites.

PubMed

Etiope, G; Ifandi, E; Nazzari, M; Procesi, M; Tsikouras, B; Ventura, G; Steele, A; Tardini, R; Szatmari, P

2018-06-07

Recurring discoveries of abiotic methane in gas seeps and springs in ophiolites and peridotite massifs worldwide raised the question of where, in which rocks, methane was generated. Answers will impact the theories on life origin related to serpentinization of ultramafic rocks, and the origin of methane on rocky planets. Here we document, through molecular and isotopic analyses of gas liberated by rock crushing, that among the several mafic and ultramafic rocks composing classic ophiolites in Greece, i.e., serpentinite, peridotite, chromitite, gabbro, rodingite and basalt, only chromitites, characterized by high concentrations of chromium and ruthenium, host considerable amounts of 13 C-enriched methane, hydrogen and heavier hydrocarbons with inverse isotopic trend, which is typical of abiotic gas origin. Raman analyses are consistent with methane being occluded in widespread microfractures and porous serpentine- or chlorite-filled veins. Chromium and ruthenium may be key metal catalysts for methane production via Sabatier reaction. Chromitites may represent source rocks of abiotic methane on Earth and, potentially, on Mars.

Mapping Hydrothermal Alterations in the Muteh Gold Mining Area in Iran by using ASTER satellite Imagery data

NASA Astrophysics Data System (ADS)

Asadi Haroni, Hooshang; Hassan Tabatabaei, Seyed

2016-04-01

Muteh gold mining area is located in 160 km NW of Isfahan town. Gold mineralization is meso-thermal type and associated with silisic, seresitic and carbonate alterations as well as with hematite and goethite. Image processing and interpretation were applied on the ASTER satellite imagery data of about 400 km2 at the Muteh gold mining area to identify hydrothermal alterations and iron oxides associated with gold mineralization. After applying preprocessing methods such as radiometric and geometric corrections, image processing methods of Principal Components Analysis (PCA), Least Square Fit (Ls-Fit) and Spectral Angle Mapper (SAM) were applied on the ASTER data to identify hydrothermal alterations and iron oxides. In this research reference spectra of minerals such as chlorite, hematite, clay minerals and phengite identified from laboratory spectral analysis of collected samples were used to map the hydrothermal alterations. Finally, identified hydrothermal alteration and iron oxides were validated by visiting and sampling some of the mapped hydrothermal alterations.

A field trip guidebook to the type localities of Marland Billings' 1935 Paleozoic bedrock stratigraphy near Littleton, New Hampshire

USGS Publications Warehouse

Rankin, Douglas W.; Rankin, Mary B.

2014-01-01

Marland Billings' classic paper published in 1937 in the Geological Society of America Bulletin established a succession of six stratigraphic units in rocks of low metamorphic grade near Littleton, New Hampshire. The two youngest units are fossiliferous in the area, with ages established at the time as “middle” Silurian and Early Devonian. Billings and students mapped the same stratigraphic section in adjacent areas of progressively higher regional metamorphic grade. This work laid the foundation upon which a major part of subsequent work in New England has been directly or indirectly built. This guidebook was written for a field trip held in March 2013 to visit roadcuts that are as close as possible in March to the type localities or areas of Billings’ six-fold stratigraphic succession. Ten stops are in rocks of chlorite grade of Acadian(?) metamorphism; the final stop visits amphibolite of the Ammonoosuc Volcanics. Fieldwork by the authors over the past 20 years confirms Billings’ broad conclusions.

Geology of the Bir Nifazi Quadrangle, Kingdom of Saudi Arabia

USGS Publications Warehouse

Quick, James E.; Bosch, Paul S.

1990-01-01

A north-trending, 10-km-long belt of gossans crops out within the ophiolite beneath the upper-basalt sequence at Jabal Mardah. Reconnaissance drilling indicates that one of the larger gossans is underlain by a steeply dipping, 15-m-thick, sulfide-rich volcanic wacke that averages 1 percent nickel locally. The ore is composed of pyrite, millerite, polydymite, and minor sphalerite that fill interstices between clasts of the wacke and are intimately intergrown with quartz and nickel-rich epidote and chlorite. These textures and assemblages suggest that the sulfides crystallized in situ from infiltrating hydrothermal fluids. Tuffs and basalt flows appear to have acted as impermeable barriers that channeled the hydrothermal fluids through the more permeable wacke where sulfides were deposited. Carbonate-replaced serpentinized peridotite at the base of the ophiolite is considered a potential source for the nickel. In contrast to most nickel deposits, the mineralized rocks at Jabal Mardah have extremely high Ni/Cu (130 to 260) and negligible concentrations (< 5 ppb) of platinum-group elements.

Feruvite from the Sullivan Pb-Zn-Ag deposit, British Columbia

USGS Publications Warehouse

Jiang, S.-Y.; Palmer, M.R.; McDonald, A.M.; Slack, J.F.; Leitch, C.H.B.

1996-01-01

Feruvite, an uncommon Ca- and Fe2+-rich tourmaline species, has been discovered in the footwall of the Sullivan Pb-Zn-Ag deposit (British Columbia) near gabbro sills and dikes. Its chemical composition varies according to occurrence: feruvite from the shallow footwall has lower Ca, higher Al, and higher X-site vacancies than that from the deep footwall. The major chemical substitution involved in the feruvite is the exchange vector CaMgO???-1Al-1(OH)-1. The most important factor controlling feruvite formation at Sullivan is likely the reaction of Fe-rich hydrothermal fluids with Ca-rich minerals in gabbro and host rocks. This reaction led to the breakdown of Ca-rich minerals (plagioclase and hornblende), with release of Ca to solution and its incorporation into feruvite. This process probably postdated the main stages of formation of fine-grained, intermediate schorl-dravite in the tourmalinite pipe in the footwall, and is attributed to postore intrusion of gabbro and associated albite-chlorite-pyrite alteration.

Effects of simulated clay gouges on the sliding behavior of Tennessee sandston

NASA Astrophysics Data System (ADS)

Shimamoto, Toshihiko; Logan, John M.

1981-06-01

The effects of simulated fault gouge on the sliding behavior of Tennessee sandstone are studied experimentally with special reference to the stabilizing effect of clay minerals mixed into the gouge. About 30 specimens with gouge composed of pure clays, of homogeneously mixed clay and anhydrite, or of layered clay and anhydrite, along a 35° precut are deformed dry in a triaxial apparatus at a confining pressure of 100 MPa, with a shortening rate of about 5 · 10 -4/sec, and at room temperature. Pure clay gouges exhibit only stable sliding, and the ultimate frictional strength is very low for bentonite (mont-morillonite), intermediate for chlorite and illite, and considerably higher for kaolinite. Anhydrite gouge shows violent stick-slip at 100 MPa confining pressure. When this mineral is mixed homogeneously with clays, the frictional coefficient of the mixed gouge, determined at its ultimate frictional strength, decreases monotonically with an increase in the clay content. The sliding mode changes from stick-slip to stable sliding when the frictional coefficient of the mixed clay-anhydrite gouge is lowered down below 90-95% of the coefficient of anhydrite gouge. The stabilizing effect of clay in mixed gouge is closely related to the ultimate frictional strength of pure clays; that is, the effect is conspicuous only for a mineral with low frictional strength. Only 15-20% of bentonite suppresses the violent stick-slip of anhydrite gouge. In contrast, violent stick-slip occurs even if the gouge contains as much as 75% of kaolinite. The behavior of illite and chlorite is intermediate between that of kaolinite and bentonite. Bentonite—anhydrite two-layer gouge exhibits stable sliding even when the bentonite content is only 5%. Thus, the presence of a thin, clay-rich layer in a fault zone stabilizes the behavior much more effectively than do the clay minerals mixed homogeneously with the gouge. This result brings out the mechanical significance of internal structures of a fault zone in understanding the effects of intrafault materials on the fault motion. Based on the present experimental results incorporated with some other experimental data, it is argued that although the stabilizing effect of montmorillonite and vermiculite is indeed remarkable at room temperature, the effect should be much less pronounced at elevated temperatures, due perhaps to the dewatering of the clays. In most geological environments where shallow earthquakes occur, the stabilizing effect of clays is probably not so conspicuous as to completely suppress the unstable motion of a fault.

In search of early life: Carbonate veins in Archean metamorphic rocks as potential hosts of biomarkers

NASA Astrophysics Data System (ADS)

Peters, Carl A.; Piazolo, Sandra; Webb, Gregory E.; Dutkiewicz, Adriana; George, Simon C.

2016-11-01

The detection of early life signatures using hydrocarbon biomarkers in Precambrian rocks struggles with contamination issues, unspecific biomarkers and the lack of suitable sedimentary rocks due to extensive thermal overprints. Importantly, host rocks must not have been exposed to temperatures above 250 °C as at these temperatures biomarkers are destroyed. Here we show that Archean sedimentary rocks from the Jeerinah Formation (2.63 billion yrs) and Carawine Dolomite (2.55 billion yrs) of the Pilbara Craton (Western Australia) drilled by the Agouron Institute in 2012, which previously were suggested to be suitable for biomarker studies, were metamorphosed to the greenschist facies. This is higher than previously reported. Both the mineral assemblages (carbonate, quartz, Fe-chlorite, muscovite, microcline, rutile, and pyrite with absence of illite) and chlorite geothermometry suggest that the rocks were exposed to temperatures higher than 300 °C and probably ∼400 °C, consistent with greenschist-facies metamorphism. This facies leads to the destruction of any biomarkers and explains why the extraction of hydrocarbon biomarkers from pristine drill cores has not been successful. However, we show that the rocks are cut by younger formation-specific carbonate veins containing primary oil-bearing fluid inclusions and solid bitumens. Type 1 veins in the Carawine Dolomite consist of dolomite, quartz and solid bitumen, whereas type 2 veins in the Jeerinah Formation consist of calcite. Within the veins fluid inclusion homogenisation temperatures and calcite twinning geothermometry indicate maximum temperatures of ∼200 °C for type 1 veins and ∼180 °C for type 2 veins. Type 1 veins have typical isotopic values for reprecipitated Archean sea-water carbonates, with δ13CVPDB ranging from - 3 ‰ to 0‰ and δ18OVPDB ranging from - 13 ‰ to - 7 ‰, while type 2 veins have isotopic values that are similar to hydrothermal carbonates, with δ13CVPDB ranging from - 18 ‰ to - 4 ‰ and δ18OVPDB ranging from - 18 ‰ to - 12 ‰. Evidently, the migration and entrapment of hydrocarbons occurred after peak metamorphism under temperatures congruous with late catagenesis and from fluids of different compositions. The relatively high temperatures of vein formation and the known geotectonic history of the rocks analysed suggest a probable minimum age of 1.8 billion yrs (Paleoproterozoic). Our results demonstrate that post peak-metamorphic veins provide an exciting opportunity in the search for evidence of early life. The integration of petrological and organic geochemical techniques is crucial for any future studies that use biomarkers to reconstruct the early biosphere.

A Developed Spectral Identification Tree for Mineral Mapping using Hyperspectral Data

NASA Astrophysics Data System (ADS)

Gan, Fuping; Wang, Runsheng; Yan, Bokun; Shang, Kun

2016-04-01

The relationship between the spectral features and the composition of minerals are the basis of mineral identification using hyperspectral data. The reflectance spectrum of minerals results from the systematic combination of several modes of interaction between electromagnetic energy and mineral particles in the form of reflection and absorption. Minerals tend to have absorbing features at specific wavelengths with a characteristic shape, which can be used as diagnostic indicators for identification. The spectral identification tree (SIT) method for mineral identification is developed in our research to map minerals accurately and applied in some typical mineral deposits in China. The SIT method is based on the diagnostic absorption features of minerals through comparing and statistically analyzing characteristic spectral data of minerals. We establish several levels of identification rules for the type, group and species of minerals using IF-THEN rule according to the spectral identification criteria so that the developed SIT can be further used to map minerals at different levels of detail from mineral type to mineral species. Identifiable minerals can be grouped into six types: Fe2+-bearing, Fe3+-bearing, Mn2+-bearing, Al-OH-bearing, Mg-OH-bearing and carbonate minerals. Each type can be further divided into several mineral groups. Each group contains several mineral species or specific minerals. A mineral spectral series, therefore, can be constructed as "type-group-species-specific mineral (mineral variety)" for mineral spectral identification. It is noted that the mineral classification is based mainly on spectral reflectance characteristics of minerals which may not be consistent with the classification in mineralogy. We applied the developed SIT method to the datasets acquired at the Eastern Tianshan Mountains of Xinjiang (HyMap data) and the Qulong district of Xizang (Hyperion data). In Xinjiang, the two major classes of Al-OH and Mg-OH minerals were mapped firstly. Then montmorillonite, kaolinite and muscovite were identified in the area of the Al-OH bearing minerals, and chlorite and epidote were identified in the area of the Mg-OH bearing minerals. Muscovite of rich Al and poor Al were further identified in the area of muscovite. In Xizang, Al-rich and Al-poor muscovite, kaolinite, chlorite and malachite were identified using SIT method. In all, the developed SIT method can further reduce the effect of other materials and focus on targeted minerals. In particular, the discrimination accuracy will be improved when the most diagnostic absorption spectral features are used in the developed SIT method.

Reduction And Immobilization Of Hexavalent Chromium By Microbially Reduced Fe-bearing Clay Minerals

DOE Office of Scientific and Technical Information (OSTI.GOV)

Bishop, Michael E.; Glasser, Paul; Dong, Hailiang

Hexavalent chromium (Cr6+) is a major contaminant in the environment. As a redox-sensitive element, the fate and toxicity of chromium is controlled by reduction-oxidation (redox) reactions. Previous research has shown the ability of structural Fe(II) in naturally present and chemically reduced clay minerals to reduce Cr6+ to Cr(III) as a way of immobilization and detoxification. However, it is still poorly known whether or not structural Fe(II) in biologically reduced clay minerals exhibits a similar reactivity and if so, what the kinetics and mechanisms of Cr6+ reduction are. The objective of this study was to determine the kinetics and possible mechanismsmore » of Cr6+ reduction by structural Fe(II) in microbially reduced clay minerals and the nature of reduced Cr(III). Structural Fe(III) in nontronite (NAu-2), montmorillonite (SWy-2), chlorite (CCa-2), and clay-rich sediments from the Ringold Formation of the Hanford site of Washington State, USA was first bioreduced to Fe(II) by an iron-reducing bacterium Geobacter sulfurreducens with acetate as the sole electron donor and anthraquinone-2,6-disulfate (AQDS) as electron shuttle in synthetic groundwater (pH 7). Biogenic Fe(II) was then used to reduce aqueous Cr6+ at three different temperatures, 10°, 20°, and 30°C, in order to determine the temperature dependence of the redox reaction between Cr6+ and clay-Fe(II). The results showed that nontronite and montmorillonite were most effective in reducing aqueous Cr6+ at all three temperatures. In contrast, most Fe(II) in chlorite was not reactive towards Cr6+ reduction at 10°C, though at 30°C there was some reduction. For all the clay minerals, the ratio of total Fe(II) oxidized to Cr6+ reduced was close to the expected stoichiometric value of 3. Characterization of the Cr-clay reaction product with scanning electron microscopy with focused ion beam and transmission electron microscopy with electron energy loss spectroscopy revealed that reduced chromium was possibly in the form of sub-nanometer Cr2O3 in association with residual clay minerals as micro-aggregates. This textural association was expected to minimize the chance of Cr(III) reoxidation upon exposure to oxidants. These results are important for our understanding of how various clay minerals may be used to reductively immobilize the heavy metal contaminant Cr in the environment.« less

The redox budget of crust-derived fluid phases at the slab-mantle interface

NASA Astrophysics Data System (ADS)

Malaspina, N.; Langenhorst, F.; Tumiati, S.; Campione, M.; Frezzotti, M. L.; Poli, S.

2017-07-01

The redox processes taking place in the portion of the mantle on top of the subducting slab are poorly investigated and the redox potential of crust-derived fluid phases is still poorly constrained. A case study of supra-subduction mantle affected by metasomatism from crust-derived fluid phases is represented by garnet orthopyroxenites from the Maowu Ultramafic Complex (China) deriving from harzburgite precursors metasomatised at ∼4 GPa, 750-800 °C by a silica- and incompatible trace element-rich fluid phase. This metasomatism produced poikilitic orthopyroxene and inclusion-rich garnet porphyroblasts. Solid multiphase primary micro-inclusions in garnet display negative crystal shapes and infilling minerals (spinel, ±orthopyroxene, amphiboles, chlorite, ±talc, ±mica) occur with constant modal proportions, indicating that they derive from trapped solute-rich aqueous fluids. FT-IR hyper spectral imaging analyses and Raman spectroscopy, together with X-ray microtomography performed on single inclusions indicate that liquid water is still preserved at least in some inclusions (±spinel). To investigate the redox budget of these fluid phases, we measured for the first time the Fe3+ concentration of the micron-sized precipitates of the multiphase inclusions using EELS on a TEM. Results indicate that spinel contains up to 12% of Fe3+ with respect to the total iron, amphibole about 30%, while the ratio in inclusion phases such as chlorite and phlogopite may reach 70%. The Fe3+ fraction of the host garnet is equal to that measured in spinel as also confirmed by Flank Method EPMA measurements. Forward modelling fO2 calculations indicate that the garnet orthopyroxenites record ΔFMQ = -1.8 ÷ -1.5, therefore resulting apparently more reduced with respect to metasomatised supra-subduction garnet-peridotites. On the other hand, oxygen mass balance, performed both on the Maowu hybrid orthopyroxenite and on metasomatised supra-subduction garnet peridotites, indicate that the excess of oxygen (nO2) is the same (10 mol m-3). The oxygen mass balance of the crust-derived fluids (multiphase inclusions) also indicates that the fluid precipitates are more oxidised than the host rock, reaching up to 400 mol m-3 of nO2. This suggests that even after their interaction with the metasomatic orthopyroxenites, the residual fluid phases could be potentially carrier of oxidised components when it escapes the slab-mantle interface. Because of this gradient in nO2, a metasomatic front develops from the oxidised slab to the overlying lithospheric mantle wedge passing through a transitional layer of hybrid rocks at the slab-mantle interface.

Mineralogy and geochemistry of two metamorphosed sedimentary manganese deposits, Sierra Nevada, California, USA

USGS Publications Warehouse

Flohr, M.J.K.; Huebner, J.S.

1992-01-01

Laminated to massive rhodochrosite, hausmannite, and Mn-silicates from the Smith prospect and Manga-Chrome mine, Sierra Nevada, California were deposited as ocean floor sediments associated with chert and shale. The principal lithologies at Smith are chert, argillite, rhodochrosite-, hausmannite- and chlorite-rich layers, and relatively uncommon layers of jacobsite. The Manga-Chrome mine also contains layers rich in manganoan calcite and caryopilite. Tephroite, rhodonite, spessartine, and accessory alleghanyite and sonolite formed during metamorphism. Volcaniclastic components are present at Manga-Chrome as metavolcanic clasts and as Mn-poor, red, garnet- and hematite-rich layers. There is no evidence, such as relict lithologies, that Mn was introduced into Mn-poor lithologies such as chert, limestone or mudstone. Replacement of Mn-poor phases by Mn-rich phases is observed only in the groundmass of volcanic clasts that appear to have fallen into soft Mn-rich mud. Manganiferous samples from the Smith prospect and Manga-Chrome mine have high Mn Fe and low concentrations of Ni, Cu, Zn, Co, U, Th and the rare-earth elements that are similar to concentrations reported from other ancient Mn deposits found in chert-greenstone complexes and from manganiferous sediments and crusts that are forming near modern sea floor vents. The Sierra Nevada deposits formed as precipitates of Mn-rich sediments on the sea floor, probably from mixtures of circulating hydrothermal fluids and seawater. The composition of a metabasalt from the Smith prospect is consistent with those of island-arc tholeiites. Metavolcanic clasts from the Manga-Chrome mine are compositionally distinct from the Smith metabasalt and have alkaline to calc-alkaline affinities. A back-arc basin is considered to be the most likely paleoenvironment for the formation of the Mn-rich lenses at the Manga-Chrome mine and, by association, the Smith prospect. Layers of rhodochrosite, hausmannite and chert preserve the composition and some textures of the sedimentary protoliths at both Sierra Nevada deposits. Jacobsite-rich layers probably represent a Fe-rich protolith. Caryopilite and manganoan calcite represent additional protoliths at the Manga-Chrome mine. The metamorphic assemblage prehnite-chlorite-epidote-calcite in a metabasalt from the Smith prospect constrains regional metamorphic conditions to a maximum temperature of 325??C and a pressure of 2 kbar. Slightly higher temperatures are indicated by the presence of actinolite in another metabasalt. Compositions of Mn-rich minerals in Smith samples are consistent with these metamorphic conditions. ?? 1992.

Unusual Rocks of the Yap Ridge - Metamorphosed Basal Cumulates of an Arc ?

NASA Astrophysics Data System (ADS)

Hawkins, J. W.; Castillo, P. R.; Batiza, R.

2002-12-01

The 8 to 9 km deep Yap trench, and adjacent Yap Ridge, extend from the southwest end of the Mariana Trench near 11o N, to near 7o 15' N where the trench swings west to intersect the Palau Trench. Unlike other western Pacific subduction systems, the Yap Ridge rises directly from the trench, it has no forearc, neither a remnant nor active volcanic arc, and no inclined seismic zone. The few seismic events recorded are mainly < 70 km depth. Yap Ridge crest depths range from 2.5 km to emergent; there are no emergent volcanoes. Rocks from the islands Yap and Map, are mainly strongly schistose, amphibole-rich, mafic and ultramafic rocks. Metamorphic lineations, and meter-sized mullions having lenticular cross-sections, define inclined (15o southerly dip) tectonic transport. Yap and Map schists are in greenschist facies (actinolite - chlorite - Na-plagioclase, rare titanite and epidote). Talc - tremolite schists, serpentinite, and chlorite-pyroxenite are less common. Small areas of altered andesite are present; quartz diorite and hornblende-rich gabbro occur as clasts in breccias, bomb craters yielded fragments of basalt and diabase. Scattered blankets of laterite several meters thick, and jungle, obscure many details. Deeper crustal rocks exposed on inner wall of Yap Trench, (5 - 2.5 km depths) include amphibolite (Al-hornblende-andesine-titanite) interlayered with calcite- diopside - grossularite marble, and calc-silicate gneisses. Rocks dredged from Yap Ridge include metabasite similar toYap schists, island arc tholeiite series basalt, basaltic andesite, and 2-PX gabbro. These have late Miocene ages (Beccaluva et al., AGU Mon. 23, 1980). Assuming isochemical behavior for immobile elements, protolith for mafic and ultramafic schists had high Mg# (52-83), CaO/Al2O3 0.7-6, Cr 288-1490, Ni 64-609, Zr 13-145, Y 3-28 (ppm).These data suggest picrite, high-Mg basalt, boninite, or OL-PX rich ultramafic cumulates as parents. REE data, e.g. negative slope and (La/Sm)N 0.9-1.9 indicate sub-arc PX-rich cumulates as a likely protolith (from late-Oligocene to late Miocene West Mariana Ridge ?). Basalt, andesite and gabbro have arc-like depleted HFSE and REE patterns. Yap Ridge crust probably formed in a subduction setting; the inactive trench is preserved but subduction has ended. Thick crust of the Caroline Ridge, lying outboard of the Yap Trench, may inhibit subduction. Yap Ridge schists may represent ultramafic cumulates metamorphosed when thrust over arc or forearc crust.

Sulphur isotope constraints on formation conditions of the Luiswishi ore deposit, Democratic Republic of Congo (DRC)

NASA Astrophysics Data System (ADS)

Lerouge, C.; Cailteux, J.; Kampunzu, A. B.; Milesi, J. P.; Fléhoc, C.

2005-07-01

Luiswishi is a Congo-type Neoproterozoic sediment-hosted stratiform Cu-Co ore deposit of the Central Africa Copperbelt, located northwest of Lubumbashi (DRC). The ores form two main Cu-Co orebodies hosted by the Mines Subgroup, one in the lower part of the Kamoto Formation and the other at the base of the Dolomitic Shales Formation. Sulphides occur essentially as early parallel layers of chalcopyrite and carrolite, and secondarily as late stockwork sulphides cross-cutting the bedding and the early sulphide generation. Both types of stratiform and stockwork chalcopyrite and carrolite were systematically analyzed for sulphur isotopes, along the lithostratigraphic succession of the Mine Series. The quite similar δ 34S values of stratiform sulphides and late stockwork sulphides suggest an in situ recrystallization or a slight remobilization of stockwork sulphides without attainment of isotopic equilibrium between different sulphide phases (chalcopyrite and carrolite). The distribution of δ 34S values (-14.4‰ to +17.5‰) combined with the lithology indicates a strong stratigraphic control of the sulphur isotope signature, supporting bacterial sulphate reduction during early diagenesis of the host sediments, in a shallow marine to lacustrine environment. Petrological features combined with sulphur isotopic data of sulphides at Luiswishi and previous results on nodules of anhydrite in the Mine Series indicate a dominant seawater/lacustrine origin for sulphates, precluding a possible hydrothermal participation. The high positive δ 34S values of sulphides in the lower orebody at Luiswishi, hosted in massive chloritic-dolomitic siltite (known as Grey R.A.T.), fine-grained stratified dolostone (D.Strat.) and silicified-stromatolitic dolomites alternating with chloritic-dolomitic silty beds (R.S.F.), suggest that they were probably deposited during a period of regression in a basin cut off from seawater. The variations of δ 34S values (i.e. the decrease of δ 34S values from the Kamoto Formation to the overlying Dolomitic Shales and then the slight increase from S.D.2d to S.D.3a and S.D.3b members) are in perfect agreement with the inferred lithological and transgressive-regressive evolution of the ore-hosting sedimentary rocks [Cailteux, J., 1994. Lithostratigraphy of the Neoproterozoic Shaba-type (Zaire) Roan Supergroup and metallogenesis of associated stratiform mineralization. In: Kampunzu A.B., Lubala, R.T. (Eds.), Neoproterozoic Belts of Zambia, Zaire and Namibia. Journal of African Earth Sciences 19, 279-301].

2.9-1.9 Ga paleoalterations of Archean granitic basement of the Franceville basin (Gabon)

NASA Astrophysics Data System (ADS)

Mouélé, Idalina Moubiya; Dudoignon, Patrick; El Albani, Abderrazak; Meunier, Alain; Boulvais, Philippe; Gauthier-Lafaye, François; Paquette, Jean-Louis; Martin, Hervé; Cuney, Michel

2014-09-01

The Archean granitoids in the Kiéné area, Gabon, are overlained by the Paleoproterozoic sediments of the Franceville basin (2.1 Ga). The basin is known for its high-grade uranium deposits among which some have been forming natural nuclear fission reactors. Most of the studies were dedicated to the FA-FB Paleoproterozoic sediments hosting these uranium deposits. Little is known on the Archean basement itself and specifically on the hydrous alteration events it experienced before and after the sediment deposition. The present work is focused on their petrographical, mineralogical and geochemical characterization. Dating the successive alteration events has been attempted on altered monazite crystals. Rocks in different alteration states have been sampled from eight drill cores crosscutting the Archean - Paleoproterozoic unconformity. The Archean granitoids observed in the deepest levels exhibit typical petrographical features of a propylitic alteration while they are intensely illitized up to the unconformity. The propylitic alteration is mainly pervasive but the original texture of the granitoïds is conserved in spite of the formation of new minerals: Mg-chlorite, allanite and epidote forming a typical paragenesis. The illitic alteration is much more invasive near the unconformity. The illitization process leads to the replacement of feldspars and the corrosion of quartz crysals by an illitic matrix while the ferromagnesian minerals are pseudomorphosed by a Fe-chlorite + phengite + hematite assemblage. The final fluid-rock interaction step is marked by fissural deposits of calcite and anhydrite. The δ13C isotopic data show that the fissural carbonates precipitated from diagenetic fluids enriched carbon products deriving from the maturation of organic matter. The U-Pb isotopic analyzes performed on monazite crystals have dated three distinct events: 3.0-2.9 Ga (magmatic), 2.6 Ga (propylitic alteration) and 1.9 Ga (diagenetic illitization). The calculation of geochemical mass balances suggests that the water-rock ratio during the propylitic alteration event was weak. On the contrary, it was much higher during the overprinted illitization which is characterized by an intense leaching of Na, Ca, Mg, Sr, REE and an enrichment in K, Rb,Cs. Neither the petrographic features nor the geochemical data militate for an Archean weathering event (paleosol). In the present case, diagenetic fluids have percolated from the unconformity into the basement where they overprinted the illitization processes upon the previously propylitized rocks. These fluids were probably oxidant as they are also responsible of the U mobilization which led to the formation of the ore deposits close to the FA-FB interface.

Iron speciation and isotope fractionation during silicate weathering and soil formation in an alpine glacier forefield chronosequence

NASA Astrophysics Data System (ADS)

Kiczka, Mirjam; Wiederhold, Jan G.; Frommer, Jakob; Voegelin, Andreas; Kraemer, Stephan M.; Bourdon, Bernard; Kretzschmar, Ruben

2011-10-01

The chemical weathering of primary Fe-bearing minerals, such as biotite and chlorite, is a key step of soil formation and an important nutrient source for the establishment of plant and microbial life. The understanding of the relevant processes and the associated Fe isotope fractionation is therefore of major importance for the further development of stable Fe isotopes as a tracer of the biogeochemical Fe cycle in terrestrial environments. We investigated the Fe mineral transformations and associated Fe isotope fractionation in a soil chronosequence of the Swiss Alps covering 150 years of soil formation on granite. For this purpose, we combined for the first time stable Fe isotope analyses with synchrotron-based Fe-EXAFS spectroscopy, which allowed us to interpret changes in Fe isotopic composition of bulk soils, size fractions, and chemically separated Fe pools over time in terms of weathering processes. Bulk soils and rocks exhibited constant isotopic compositions along the chronosequence, whereas soil Fe pools in grain size fractions spanned a range of 0.4‰ in δ 56Fe. The clay fractions (<2 μm), in which newly formed Fe(III)-(hydr)oxides contributed up to 50% of the total Fe, were significantly enriched in light Fe isotopes, whereas the isotopic composition of silt and sand fractions, containing most of the soil Fe, remained in the range described by biotite/chlorite samples and bulk soils. Iron pools separated by a sequential extraction procedure covered a range of 0.8‰ in δ 56Fe. For all soils the lightest isotopic composition was observed in a 1 M NH 2OH-HCl-25% acetic acid extract, targeting poorly-crystalline Fe(III)-(hydr)oxides, compared with easily leachable Fe in primary phyllosilicates (0.5 M HCl extract) and Fe in residual silicates. The combination of the Fe isotope measurements with the speciation data obtained by Fe-EXAFS spectroscopy permitted to quantitatively relate the different isotope pools forming in the soils to the mineral weathering reactions which have taken place at the field site. A kinetic isotope effect during the Fe detachment from the phyllosilicates was identified as the dominant fractionation mechanism in young weathering environments, controlling not only the light isotope signature of secondary Fe(III)-(hydr)oxides but also significantly contributing to the isotope signature of plants. The present study further revealed that this kinetic fractionation effect can persist over considerable reaction advance during chemical weathering in field systems and is not only an initial transient phenomenon.

A middle Permian ophiolite fragment in Late Triassic greenschist- to blueschist-facies rocks in NW Turkey: An earlier pulse of suprasubduction-zone ophiolite formation in the Tethyan belt

NASA Astrophysics Data System (ADS)

Topuz, Gültekin; Okay, Aral I.; Schwarz, Winfried H.; Sunal, Gürsel; Altherr, Rainer; Kylander-Clark, Andrew R. C.

2018-02-01

The Eastern Mediterranean region within the Tethyan belt is characterised by two main pulses of suprasubduction-zone ophiolite formation during the Early-Middle Jurassic and Late Cretaceous. Despite vast exposures of the Permo-Triassic accretionary complexes, related suprasubduction-zone ophiolites and the timing of subduction initiation leading to the formation of Permo-Triassic accretionary complexes are unknown so far. Here we report on a 40 km long and 0.3 to 1.8 km wide metaophiolite fragment within transitional greenschist- to blueschist-facies oceanic rocks from NW Turkey. The metaophiolite fragment is made up mainly of serpentinite and minor dykes or stocks of strongly sheared metagabbro with mineral assemblages involving actinolite/winchite, chlorite, epidote, albite, titanite and phengite. The metagabbro displays (i) variable CaO and MgO contents, (ii) anomalously high Mg# (= 100 ∗ molar MgO/(MgO + FeOtot)) of 75-88, and (iii) positive Eu anomalies, together with low contents of incompatible elements such as Ti, P and Zr, suggesting derivation from former plagioclase cumulates. The serpentinites comprise serpentine, ± chlorite, ± talc, ± calcite and relict Cr-Al spinel surrounded by ferrichromite to magnetite. Relict Cr-Al spinels are characterised by (i) Cr/(Cr + Al) ratios of 0.45-0.56 and Mg/(Mg + Fe2 +) ratio of 0.76-0.22, (ii) variable contents of ZnO and MnO, and (iii) extremely low TiO2 contents. Zn and Mn contents are probably introduced into Cr-Al spinels during greenschist- to blueschist metamorphism. Compositional features of the serpentinite such as (i) Ca- and Al-depleted bulk compositions, (ii) concave U-shaped, chondrite-normalised rare earth element patterns (REE) with enrichment of light and heavy REEs, imply that serpentinites were probably derived from depleted peridotites which were refertilised by light rare earth element enriched melts in a suprasubduction-zone mantle wedge. U-Pb dating on igneous zircons from three metagabbro samples indicates igneous crystallisation at 262 Ma (middle Permian). Timing of the metamorphism is constrained by incremental 40Ar/39Ar dating on phengitic white mica at 201 Ma (latest Triassic). We conclude that the metaophiolite represents a fragment of middle Permian suprasubduction-zone oceanic lithosphere, involved in a latest Triassic subduction zone. These data, together with several reports in literature, indicate that the middle Permian was a time of suprasubduction-zone ophiolite formation in the Tethyan belt.

Minerals and clay minerals assemblages in organic-rich facies: the case study of the Sinemurian-Pliensbachian carbonate deposits of the western Lusitanian Basin (Portugal)

NASA Astrophysics Data System (ADS)

Caniço, Ana; Duarte, Luís V.; Silva, Ricardo L.; Rocha, Fernando; Graciano Mendonça Filho, João

2015-04-01

The uppermost Sinemurian-Pliensbachian series of the western part of the Lusitanian Basin is composed by hemipelagic carbonates particularly enriched in organic matter. Great part of this succession, considered to be one of the most important potential source rock intervals of Portugal, crops out in the S. Pedro de Moel and Peniche sectors, belonging to the Água de Madeiros and Vale das Fontes formations. In this study, supported by a detailed and integrated stratigraphic framework, we analyzed 98 marly samples (whole-rock mineralogy and clay minerals assemblages) from the aforementioned formations in the S. Pedro de Moel and Peniche sectors. X-ray Diffraction analysis followed the standard procedures and the semi-quantification of the different mineral phases was calculated using MacDiff 4.2.6. The goals of this work are to demonstrate the vertical variability of the mineral composition of these two units and investigate the relationship between the clay minerals assemblages and the content in organic matter (Total organic carbon: TOC). Besides the abundance of calcite and phyllosilicates, whole-rock mineralogy revealed the presence of quartz, potassium feldspar, dolomite, and pyrite (trace amounts). Other minerals like anhydrite, barite and gypsum occur sporadically. The clay minerals assemblages are dominated by illite+illite/smectite mixed-layers (minimum of 59%), always associated with kaolinite (maximum of 37%) and chlorite (maximum of 25%); sporadically smectite occurs in trace amounts. Generally, high TOC levels (i.e., black shale facies with TOC reaching up to 22 wt.% in both units, see Duarte et al., 2010), show a major increase in chlorite and kaolinite (lower values of illite+illite/smectite mixed layers). A kaolinite enrichment is also observed just above the Sinemurian-Pliensbachian boundary (base of Praia da Pedra Lisa Member of Água de Madeiros Formation; values varying between 30 and 37%). This event is associated with a second-order regressive phase, and marks the disappearance of the organic-rich facies and increase of carbonate sedimentation. This enrichment was likely favored by the development of more humid conditions at the Sinemurian-Pliensbachian transition. References Duarte, L.V., Silva, R.L., Oliveira, L.C.V., Comas-Rengifo, M.J., Silva, F. 2010. Organic-rich facies in the Sinemurian and Pliensbachian of the Lusitanian Basin, Portugal: Total Organic Carbon distribution and relation to transgressive-regressive facies cycles. Geologica Acta 8, 325-340.

Hydrothermal alteration and Cu–Ni–PGE mobilization in the charnockitic rocks of the footwall of the South Kawishiwi intrusion, Duluth Complex, USA

PubMed Central

Benkó, Zsolt; Mogessie, Aberra; Molnár, Ferenc; Krenn, Kurt; Poulson, Simon R.; Hauck, Steven; Severson, Mark; Arehart, Greg B.

2015-01-01

In the Neoarchean (~ 2.7 Ga) contact metamorphosed charnockitic footwall of the Mesoproterosoic (1.1 Ga) South Kawishiwi intrusion of the Duluth Complex, the primary metamorphic mineral assemblage and Cu–Ni–PGE sulfide mineralization is overprinted by an actinolite + chlorite + cummingtonite + prehnite + pumpellyite + quartz + calcite hydrothermal mineral assemblage along 2–3 cm thick veins. In calcite, hosted by the hydrothermal alteration zones and in a single recrystallized quartz porphyroblast, four different fluid inclusion assemblages are documented; the composition of these fluid inclusions provide p–T conditions of the fluid flow, and helps to define the origin of the fluids and evaluate their role in the remobilization and reprecipitation of the primary metamorphic sulfide assemblage. Pure CO2 fluid inclusions were found as early inclusions in recrystallized quartz porphyroblast. These inclusions may have been trapped during the recrystallization of the quartz during the contact metamorphism of the footwall charnockite in the footwall of the SKI. The estimated trapping pressure (1.6–2.0 kbar) and temperature (810–920 °C) conditions correspond to estimates based on felsic veins in the basal zones of the South Kawishiwi intrusion. Fluid inclusion assemblages with CO2–H2O–NaCl and CH4–N2–H2O–NaCl compositions found in this study along healed microfractures in the recrystallized quartz porphyroblast establish the heterogeneous state of the fluids during entrapment. The estimated trapping pressure and temperature conditions (240–650 bar and 120–150 °C for CO2–H2O–NaCl inclusions and 315–360 bar and 145–165 °C for CH4–N2–H2O–NaCl inclusions) are significantly lower than the p–T conditions (> 700 °C and 1.6–2 kbar) during the contact metamorphism, indicating that this fluid flow might not be related to the cooling of the Duluth Complex and its contact aureole. The presence of chalcopyrite inclusions in these fluid inclusions and in the trails of these fluid inclusion assemblages confirms that at least on local scale these fluids played a role in base metal remobilization. No evidences have been observed for PGE remobilization and transport in the samples. The source of the carbonic phase in the carbonic assemblages (CO2; CH4) could be the graphite, present in the metasedimentary hornfelsed inclusions in the basal zones of the South Kawishiwi intrusion. The hydrothermal veins in the charnockite can be characterized by an actinolite + cummingtonite + chlorite + prehnite + pumpellyite + calcite (I–II) + quartz mineral assemblage. Chlorite thermometry yields temperatures around 276–308 °C during the earliest phase of the fluid flow. In the late calcite (II) phase, high salinity (21.6–28.8 NaCl + CaCl2 equiv. wt.%), low temperature (90–160 °C), primary aqueous inclusions were found. Chalcopyrite (± sphalerite ± millerite), replacing and intersecting the early hydrothermal phases, are associated to the late calcite (II) phase. The composition of the formational fluids in the Canadian Shield is comparable with the composition of the studied fluid inclusions. This suggests that the composition of the fluids did not change in the past 2 Ga and base metal remobilization by formational fluids could have taken place any time after the formation of the South Kawishiwi intrusion. Sulfur isotope studies carried out on the primary metamorphic (δ34S = 7.4–8.9‰) and the hydrothermal sulfide mineral assemblage (δ34S = 5.5–5.7‰) proves, that during the hydrothermal fluid flow the primary metamorphic ores were remobilized. PMID:26594080

Composition and properties of the Pierre Shale and equivalent rocks, northern Great Plains region

USGS Publications Warehouse

Schultz, Leonard Gene; Tourtelot, H.A.; Gill, J.R.; Boerngen, J.G.

1980-01-01

The Pierre Shale and equivalent rocks of Late Cretaceous age consist in the east-central Dakotas of several hundred feet of offshore-marine shale and minor marl; in west-central Montana near the sediment source the equivalents of the Pierre Shale consist of several thousand feet of volcanic-rich and mostly nonmarine sediments; and in the area between, both types of rock are separated by tongues of nearshore-marine siltstone and sandstone that mark three major transgressions of the sea across the area. The major-, minor-, and trace-element composition was determined for 226 samples of these rocks, and the mineralogical composition was determined for 1,350 samples. Slurry pH, Atterberg limits, and grain and bulk densities were determined on some samples. The arithmetic mean, in percent, and standard deviation (in parentheses) of major and minor elements, mostly in shale and siltstone and excluding the 23 chemically analyzed bentonite samples, are as follows: SiO2 60.8 (7.9) Al2O3 14.4 (2.5) Fe2O3 3.4 (1.4) FeO 1.1 (1.2) MgO 2.2 (1.0) CaO 2.7 (0.48) Na2O 1.1 (0.56) K2O 2.4 (0.57) H2O- 3.2 (1.3) H2O+ 4.3 (1.2) TiO2 0.58 (0.12) P2O5 0.14 (0.073) S 0.37 (1.1) F 0.71 (0.15) Cl 0.16 (0.024) CO2 2.1 (7.0) C, organic 0.94 (1.8) The mean and standard deviation of minerals as determined by X-ray methods, excluding bentonite samples, is as follows: clay minerals, 53 (20); quartz, 24 (13); cristobalite, 1 (5); potassium-feldspar, 1 (2); plagioclase, 6 (7); anorthite content from 20 to 40 percent; calcite, 5 (14); dolomite, 4 (7); organic matter, 1 (2); and sparsely scattered gypsum, jarosite, pyrite, zeolites, augite, siderite, and probably minor amounts of hydrated iron-manganese (Fe-Mn) oxides. The mean and standard deviation of the clay-mineral fraction is as follows: mixed-layer illite-smectite, 70 (20); illite, 16 (9); chlorite, 3 (6); and kaolinite, 9 (13). The mixed-layer clay, except in the Montana disturbed belt, is a random interlayering of 20 to 60 percent illite-type layers, about 35 percent beidelite-type layers, and the remainder montmorillonite-type layers; chlorite or vermiculite layers are rare. Most bentonite differs from shale in its small quartz content, rarely more than a few percent, in the more calcic composition and hightemperature thermal state of its plagioclase, and in its rare kaolinite, near absence of chlorite, and lack of illite-either free or mixed layered with smectite. Bentonite commonly consists of more than 90 percent smectite in which montmorillonite is interlayered with a smaller amount of beidellite. The clay-mineral composition of marine rock, including proportions of layers in the dominant illite-smectite, averages about the same as in the nonmarine rock, though in the latter the composition is more variable. The average content of major chemical constituents also is closely similar, partly because the large clay content of fine-grained offshore-marine shale is balanced by the small clay content of nearshore-marine siltstone and sandstone. In addition, the alumina and alkalic elements in an average of 10 percent more clay in marine rock are partly balanced by these constituents in the 5 percent more feldspar in nonmarine rock. Much of the observed regional and stratigraphic variation in maj or constituents is the result of the three major east-west migrations of the depositional sites of nearshore-marine sandstone and siltstone. Dolomite is found almost exclusively in relatively coarse-grained rock, particularly in nearshore-marine siltstone where diagenetic dolomite is expected, but it is found almost as frequently in nonmarine siltstone. Amounts of minor constituents are nearly equal in marine and nonmarine rocks, except that pyrite and consequently sulfur are relatively sparse in nonmarine rock. Average amounts of organic matter found in marine and nonmarine rocks are nearly identical. However, organic matter in nonmarine rock occurs almost entirely in volumetric

Using ASD data to identify the altered minerals for exploring of gold deposit in the Beishan area, North China

NASA Astrophysics Data System (ADS)

Ren, G. L.; Yi, H.; Yang, M.; Liang, N.; Li, J. Q.; Yang, J. L.

2016-11-01

Hyperspectral information of altered minerals plays an important role in the identifications of mineralized zones. In this study, the altered minerals of two gold deposits from Fangshankou-Laojinchang regions of Beishan metallogenic belt were measured by ASD field Spectrometer. Many gold deposits would have a close relationship with Variscan magma intrusion, which have been found in study region. The alteration minerals have been divided six types by the spectral results, i.e. sericite, limonite, dolomite, chlorite, epidote and calcite. The distribution characteristics and formations of altered minerals were discussed here. By the ASD, the spectral curve of different geological units in the Jintanzi and Fangshankou gold deposits were analysed and summarized. The results show that the sericite and limonite are mainly related with the gold mineralization and widely occurred in the gold deposits. Therefore, we proposed that the sericite and limonite are the iconic alteration mineral assemblages for gold mineralization and the models of altered minerals for gold deposits could be established in this region.

Analysis of ERTS-1 linear features in New York State

NASA Technical Reports Server (NTRS)

Isachsen, Y. W. (Principal Investigator); Fakundiny, R. H.; Forster, S. W.

1974-01-01

The author has identified the following significant results. All ERTS-1 linears confirmed to date have topographic expression although they may appear as featureless tonal linears on the imagery. A bias is unavoidably introduced against any linears which may parallel raster lines, lithological trends, or the azimuth of solar illumination. Ground study of ERTS-1 topographic lineaments in the Adirondacks indicates: outcrops along linears are even more rare than expected, fault breccias are found along some NNE lineaments, chloritization and slickensiding without brecciation characterize one EW lineament whereas closely-spaced jointing plus a zone of plastic shear define another. Field work in the Catskills suggests that the prominent new NNE lineaments may be surface manifestations of normal faulting in the basement, and that it may become possible to map major joint sets over extensive plateau regions directly on the imagery. Fall and winter images each display some unique linears, and long linears on the fall image commonly appear as aligned segments on the winter scene. A computer-processed color composite image permitted the extraction or additional information on the shaded side of mountains.

Chemical modification of cellulose-rich fibres to clarify the influence of the chemical structure on the physical and mechanical properties of cellulose fibres and thereof made sheets.

PubMed

López Durán, Verónica; Larsson, Per A; Wågberg, Lars

2018-02-15

Despite the different chemical approaches used earlier to increase the ductility of fibre-based materials, it has not been possible to link the chemical modification to their mechanical performance. In this study, cellulose fibres have been modified by periodate oxidation, alone or followed either by borohydride reduction, reductive amination or chlorite oxidation. In addition, TEMPO oxidation, and TEMPO oxidation in combination with periodate oxidation and further reduction with sodium borohydride have also been studied. The objective was to gain understanding of the influence of different functional groups on the mechanical and structural properties of handsheets made from the modified fibres. It was found that the modifications studied improved the tensile strength of the fibres to different extents, but that only periodate oxidation followed by borohydride reduction provided more ductile fibre materials. Changes in density, water-holding capacity and mechanical performance were also quantified and all are dependent on the functional group introduced. Copyright © 2017 Elsevier Ltd. All rights reserved.

Mapping alteration using imagery from the Tiangong-1 hyperspectral spaceborne system: Example for the Jintanzi gold province, China

NASA Astrophysics Data System (ADS)

Liu, Lei; Feng, Jilu; Rivard, Benoit; Xu, Xinliang; Zhou, Jun; Han, Ling; Yang, Junlu; Ren, Guangli

2018-02-01

The Tiangong-1 Hyperspectral Imager (HSI) is a relatively new spaceborne hyperspectral remote sensing system that was launched by the Chinese government on September 29th 2011. The system has 64 shortwave infrared (SWIR) spectral bands (1000-2500 nm) and imagery is at a spatial resolution of 20 m. This study represents an evaluation of Tiangong-1 data for the production of alteration mineral maps. Alteration mineral maps resulting from the analysis of Tiangong-1 HSI data and airborne SASI (Shortwave infrared Airborne Spectrographic Imager) data are compared for the Jintanzi area, Beishan, Gansu province, northwest China where gold bearing veins are documented. The results illustrate the detection of muscovite, kaolinite, chlorite, epidote, calcite and dolomite from Tiangong-1 HSI data and most anomalies seen in the airborne SASI data are captured. The Tiangong-1 data appears to be well suited for the detection of surface mineralogy in support of regional mapping and exploration. The data complements that which will be offered by the Chinese GF-5 Hyperspectral Imager and the German EnMAP system, both scheduled for launch in 2018.

A mineralogical petrographic and geochemical study of samples from wells in the geothermal field of Milos Island (Greece)

DOE Office of Scientific and Technical Information (OSTI.GOV)

Liakopoulos, A.

1991-01-01

This paper presents a study of hydrothermal alteration on Milos Island, Greece. Examination of cores and cuttings from the two drill sites, obtained from a depth of about 1100 m in Milos geothermal field, showed that the hydrothermal minerals occurring in the rock include: K-feldspar, albite, chlorite, talc, diopside, epidote, muscovite, tremolite, kaolinite, montmorillonite, alunite, anhydrite, gypsum, calcite, and opaque minerals. The chemical composition of the minerals (104 analyses) was determined with Electron Probe Microanalysis. The composition of the hydrothermal fluid was determined and correlated with the mineralogy. Isotopic ratios of C and O for one calcite sample taken frommore » 341 m depth were determined and used for geochemical calculations. A number of reactions feasible at the P-T conditions of the geothermal field are given to establish the chemical evolution of the hydrothermal fluid. The distribution of the hydrothermal minerals indicates the dilution of the K-, Na- Cl-rich hydrothermal fluid of the deep reservoir by a Ca-, Mg-rich cold water at a shallower level.« less

Global distribution of clay-size minerals on land surface for biogeochemical and climatological studies

PubMed Central

Ito, Akihiko; Wagai, Rota

2017-01-01

Clay-size minerals play important roles in terrestrial biogeochemistry and atmospheric physics, but their data have been only partially compiled at global scale. We present a global dataset of clay-size minerals in the topsoil and subsoil at different spatial resolutions. The data of soil clay and its mineralogical composition were gathered through a literature survey and aggregated by soil orders of the Soil Taxonomy for each of the ten groups: gibbsite, kaolinite, illite/mica, smectite, vermiculite, chlorite, iron oxide, quartz, non-crystalline, and others. Using a global soil map, a global dataset of soil clay-size mineral distribution was developed at resolutions of 2' to 2° grid cells. The data uncertainty associated with data variability and assumption was evaluated using a Monte Carlo method, and validity of the clay-size mineral distribution obtained in this study was examined by comparing with other datasets. The global soil clay data offer spatially explicit studies on terrestrial biogeochemical cycles, dust emission to the atmosphere, and other interdisciplinary earth sciences. PMID:28829435

Quintinite-1 M from the Mariinsky Deposit, Ural Emerald Mines, Central Urals, Russia

NASA Astrophysics Data System (ADS)

Zhitova, E. S.; Popov, M. P.; Krivovichev, S. V.; Zaitsev, A. N.; Vlasenko, N. S.

2017-12-01

The paper describes the first finding of quintinite [Mg4Al2(OH)12][(CO3)(H2O)3] at the Mariinsky deposit in the Central Urals, Russia. The mineral occurs as white tabular crystals in cavities within altered gabbro in association with prehnite, calcite, and a chlorite-group mineral. Quintinite is the probable result of late hydrothermal alteration of primary mafic and ultramafic rocks hosting emerald-bearing glimmerite. According to electron microprobe data, the Mg: Al ratio is 2: 1. IR spectroscopy has revealed hydroxyl and carbonate groups and H2O molecules in the mineral. According to single crystal XRD data, quintinite is monoclinic, space group C2/ m, a =5.233(1), b = 9.051(2), c = 7.711(2) Å, β = 103.09(3)°, V = 355.7(2) Å3. Based on structure refinement, the polytype of quintinite should be denoted as 1M. This is the third approved occurrence of quintinite-1M in the world after the Kovdor complex and Bazhenovsky chrysotile-asbestos deposit.

Modern halolites (halite oolites) in the Tuz Gölü, Turkey

NASA Astrophysics Data System (ADS)

Tekin, E.; Ayyildiz, T.; Gündoğan, İ.; Orti, F.

2007-03-01

Halite oolites (halolites) and pisoids (halopisoids) precipitate yearly (in summer) in the brine conduits of the saltpans in the Tuz Gölü saline lake (Central Anatolia, Turkey). These halolites are well rounded and spherical, ranging between 0.7 and 2 cm in size. They are composed of coarse-grained halite crystals as the nucleus, and by concentric halite laminae with a radial fabric as the cortex. The cortex is subdivided into inner, middle, and outer zones, each zone showing different mineralogical and morphological features. These features include the presence of: organic matter particles, native sulphur globules, gypsum-anhydrite-calcite laminae, quartz-chlorite-celestite-thermonatrite laminae, submicroscopic halite crystals, and microborings, cavities and corrosion-like structures. Our observations in the Tuz Gölü saltpan environment and in the halolite fabrics suggest that (1) an intermittent supply of heavy brines from the saline lake into the saltpan conduits, which occur under agitated conditions during pumping operations, is the main genetic reason for the halolite formation; and that (2) physical, chemical and biological factors exert a significant influence on the mineralogical-textural complexity of the cortex.

Influence of thermal effects on buoyancy-driven convection around autocatalytic chemical fronts propagating horizontally.

PubMed

Rongy, L; Schuszter, G; Sinkó, Z; Tóth, T; Horváth, D; Tóth, A; De Wit, A

2009-06-01

The spatiotemporal dynamics of vertical autocatalytic fronts traveling horizontally in thin solution layers closed to the air can be influenced by buoyancy-driven convection induced by density gradients across the front. We perform here a combined experimental and theoretical study of the competition between solutal and thermal effects on such convection. Experimentally, we focus on the antagonistic chlorite-tetrathionate reaction for which solutal and thermal contributions to the density jump across the front have opposite signs. We show that in isothermal conditions the heavier products sink below the lighter reactants, providing an asymptotic constant finger shape deformation of the front by convection. When thermal effects are present, the hotter products, on the contrary, climb above the reactants for strongly exothermic conditions. These various observations as well as the influence of the relative weight of the solutal and thermal effects and of the thickness of the solution layer on the dynamics are discussed in terms of a two-dimensional reaction-diffusion-convection model parametrized by a solutal R(C) and a thermal R(T) Rayleigh number.

Preparation of micro-fibrillated cellulose based on sugar palm ijuk (Arenga pinnata) fibres through partial acid hydrolysis

NASA Astrophysics Data System (ADS)

Saputro, A.; Verawati, I.; Ramahdita, G.; Chalid, M.

2017-07-01

The aim of this study was to isolate and characterized micro-fibrillated cellulose (MFC) from sugar palm/ijuk fibre (Arenga pinnata) by partial sulfuric acid hydrolysis. Cellulose fibre was prepared by repeated treatments with 5 wt% sodium hydroxide 2 h at 80°C, followed by bleaching with 1.7 wt% sodium chlorite for 2 h at 80°C in acidic environment under stirring. MFC was prepared by partial hydrolysis with sulfuric acid in various concentrations (30, 40, 50, and 60 % for 45 min at 45 °C) under stirring. Fourier Transform Infrared, Field Emission Scanning Electron Microscope, Thermo Gravimetric Analyzer and X-ray Diffraction characterized cellulose fibre and MFC. FTIR measurements showed that alkaline and bleaching treatments were effective to remove non-cellulosic constituents such as wax, lignin and hemicellulose. FESEM observation revealed conversion into more clear surface and defibrillation of cellulosic fibre after pre-treatments. XRD measurement revealed increase in crystallinity after pre-treatments and acid hydrolysis from 54.4 to 87.8%. Thermal analysis showed that increasing acid concentration reduced thermal stability.

Clay minerals in sediments of Portuguese reservoirs and their significance as weathering products from over-eroded soils: a comparative study of the Maranhão, Monte Novo and Divor Reservoirs (South Portugal)

NASA Astrophysics Data System (ADS)

Fonseca, Rita M. F.; Barriga, Fernando J. A. S.; Conceição, Patrícia I. S. T.

2010-12-01

The Southern region of Portugal is subjected to several forms of over-erosion. Most leached products, mainly composed of fine particles containing nutrients, metals or pesticides, are easily transported by river flows. When these are hindered by a physical barrier such as a dam, the particulate load accumulates on the bottom of the reservoirs, often leading to a pronounced decrease of water quality. Bottom sediments from three reservoirs were subjected to grain-size analysis and a study of clay minerals by X-ray diffraction. Most sediments contain a diverse set of clay minerals, mostly illites, smectites, chlorites and kaolinites. The nature of the clay minerals reflects the nature of the parent rocks. During the cycles of transport and temporary deposition, they may undergo significant chemical and physical transformations, which lead to an increase of expandable properties and therefore, to a higher cationic exchange capacity, determining its important role as vehicles of environmental pollutants.

Evidence of phyllosilicates in Wooly Patch, an altered rock encountered at West Spur, Columbia Hills, by the Spirit rover in Gusev crater, Mars

USGS Publications Warehouse

Wang, A.; Korotev, R.L.; Jolliff, B.L.; Haskin, L.A.; Crumpler, L.; Farrand, W. H.; Herkenhoff, K. E.; de Souza, Jr.; Kusack, A.G.; Hurowitz, J.A.; Tosca, N.J.

2006-01-01

On its traverse to Columbia Hills, the Mars Exploration Rover Spirit investigated an outcrop designated "Wooly Patch" that exhibited morphological, mineralogical, and geochemical characteristics at the extreme ends of ranges observed among rocks studied at West Spur, a westward projecting salient near the foot of the Columbia Hills, Gusev crater. The major-element composition and Fe-mineralogy, as determined by the Alpha-Particle X-ray Spectrometer and Mo??ssbauer Spectrometer, are inconsistent with any reasonable assemblage of basaltic minerals in that there is an excess of Si and Al. The combined data are best explained by the presence of 14-17% phyllosilicate minerals. Phyllosilicates that account for the composition and cation ratios include members of the kaolinite, serpentine, chlorite, and septechlorite groups. The potential existence of kaolinite-type Al-rich phyllosilicates within the Wooly Patch outcrop suggests a mildly acidic environment (pH 4-6) in the past and an open hydrologic system with good drainage conditions in the environment where these rocks were altered. Copyright 2006 by the American Geophysical Union.

Short-wave infrared reflectance investigation of sites of paleobiological interest: applications for Mars exploration.

PubMed

Brown, Adrian; Walter, Malcolm; Cudahy, Thomas

2004-01-01

Rover missions to the rocky bodies of the Solar System and especially to Mars require lightweight, portable instruments that use minimal power, require no sample preparation, and provide suitably diagnostic mineralogical information to an Earth-based exploration team. Short-wave infrared (SWIR) spectroscopic instruments such as the Portable Infrared Mineral Analyser (PIMA, Integrated Spectronics Pty Ltd., Baulkham Hills, NSW, Australia) fulfill all these requirements. We describe an investigation of a possible Mars analogue site using a PIMA instrument. A survey was carried out on the Strelley Pool Chert, an outcrop of stromatolitic, silicified Archean carbonate and clastic succession in the Pilbara Craton, interpreted as being modified by hydrothermal processes. The results of this study demonstrate the capability of SWIR techniques to add significantly to the geological interpretation of such hydrothermally altered outcrops. Minerals identified include dolomite, white micas such as illite-muscovite, and chlorite. In addition, the detection of pyrophyllite in a bleached and altered unit directly beneath the succession suggests acidic, sulfur-rich hydrothermal activity may have interacted with the silicified sediments of the Strelley Pool Chert.

Observations on Cretaceous abyssal hills in the northeast Pacific

USGS Publications Warehouse

Eittreim, S.L.; Piper, D.Z.; Chezar, H.; Jones, D.R.; Kaneps, A.

1984-01-01

An abyssal hills area of 50 ?? 60 km in the northeast Pacific was studied using bottom transponder navigation, closely spaced survey lines, and long-traverse oblique photography. The block-faulted north-south hills are bounded by scarps, commonly with 40?? slopes. On these steep scarps sedimentation is inhibited and pillow basalts often crop out. An ash layer of high acoustic reflectivity at about 7 m subbottom depth blankets the area. This ash occurs in multiple beds altered to phillipsite and is highly consolidated. A 24 m.y. age for the ash is based on ichthyolith dates from samples in the overlying sediments. Acoustically transparent Neogene sediments above the ash are thickest in trough bottoms and are absent or thin on steep slopes. These Neogene sediments are composed of pale-brown pelagic clays of illite, quartz, smectite, chlorite and kaolinite. Dark-brown pelagic clays, rich in smectite and amorphous iron oxides, underlie the Neogene surficial sediments. Manganese nodules cover the bottom in varying percentages. The nodules are most abundant near basement outcrops and where the subbottom ash layer is absent. ?? 1984.

Geochemistry of vanadium in an epigenetic, sandstone-hosted vanadium- uranium deposit, Henry Basin, Utah

USGS Publications Warehouse

Wanty, R.B.; Goldhaber, M.B.; Northrop, H.R.

1990-01-01

The epigenetic Tony M vanadium-uranium orebody in south-central Utah is hosted in fluvial sandstones of the Morrison Formation (Upper Jurassic). Measurements of the relative amounts of V+3 and V +4 in ore minerals show that V+3 is more abundant. Thermodynamic calculations show that vanadium was more likely transported to the site of mineralization as V+4. The ore formed as V+4 was reduced by hydrogen sulfide, followed by hydrolysis and precipitation of V+3 in oxide minerals or chlorite. Uranium was transported as uranyl ion (U+6), or some complex thereof, and reduced by hydrogen sulfide, forming coffinite. Detrital organic matter in the rocks served as the carbon source for sulfate-reducing bacteria. Vanadium most likely was derived from the dissolution of iron-titanium oxides. Uranium probably was derived from the overlying Brushy Basin Member of the Morrison Formation. Previous studies have shown that the ore formed at the density-stratified interface between a basinal brine and dilute meteoric water. The mineralization processes described above occurred within the mixing zone between these two fluids. -from Authors

CO2–rock–brine interactions in Lower Tuscaloosa Formation at Cranfield CO2 sequestration site, Mississippi, U.S.A.

USGS Publications Warehouse

Lu, Jiemin; Kharaka, Yousif K.; Thordsen, James J.; Horita, Juske; Karamalidis, Athanasios; Griffith, Craig; Hakala, J. Alexandra; Ambats, Gil; Cole, David R.; Phelps, Tommy J.; Manning, Michael A.; Cook, Paul J.; Hovorka, Susan D.

2012-01-01

A highly integrated geochemical program was conducted at the Cranfield CO2-enhanced oil recovery (EOR) and sequestration site, Mississippi, U.S.A.. The program included extensive field geochemical monitoring, a detailed petrographic study, and an autoclave experiment under in situ reservoir conditions. Results show that mineral reactions in the Lower Tuscaloosa reservoir were minor during CO2 injection. Brine chemistry remained largely unchanged, which contrasts with significant changes observed in other field tests. Field fluid sampling and laboratory experiments show consistently slow reactions. Carbon isotopic composition and CO2 content in the gas phase reveal simple two-end-member mixing between injected and original formation gas. We conclude that the reservoir rock, which is composed mainly of minerals with low reactivity (average quartz 79.4%, chlorite 11.8%, kaolinite 3.1%, illite 1.3%, concretionary calcite and dolomite 1.5%, and feldspar 0.2%), is relatively unreactive to CO2. The significance of low reactivity is both positive, in that the reservoir is not impacted, and negative, in that mineral trapping is insignificant.

Chemical composition and osmium-isotope systematics of primary and secondary PGM assemblages from high-Mg chromitite of the Nurali lherzolite massif, the South Urals, Russia

NASA Astrophysics Data System (ADS)

Malitch, K. N.; Anikina, E. V.; Badanina, I. Yu.; Belousova, E. A.; Pushkarev, E. V.; Khiller, V. V.

2016-01-01

The isotopic and geochemical characteristics of PGE mineralization in high-Mg chromitite from the banded dunite-wehrlite-clinopyroxenite complex of the Nurali lherzolite massif, the South Urals, Russia is characterized for the first time. Electron microprobe analysis and LA MC-ICP-MS mass spectrometry are used for studying Cr-spinel and platinum-group minerals (PGM). Two processes synchronously develop in high-Mg chromitite subject to metamorphism: (1) the replacement of Mg-Al-rich Cr-spinel, orthopyroxene, and diopside by chromite, Cr-amphibole, chlorite, and garnet; (2) the formation of a secondary mineral assemblage consisting of finely dispersed ruthenium or Ru-hexaferrum aggregate and silicate-oxide or silicate matter on the location of primary Ru-Os-sulfides of the laurite-erlichmanite solid solution series. Similar variations of Os-isotopic composition in both primary and secondary PGM assemblages are evidence for the high stability of the Os isotope system in PGM and for the possibility of using model 187Os/188Os ages in geodynamic reconstructions.

Evidence of the impacting body of the Ries crater - the discovery of Fe-Cr-Ni veinlets below the crater bottom

USGS Publications Warehouse

El, Goresy A.; Chao, E.C.T.

1976-01-01

Fe-Cr-Ni particles and veinlets have been discovered in the top 15 m of the compressed zone with abundant shatter cones below the bottom of the Ries crater. The metallic particles are less than a few microns across. They occur in various minerals along healed intergranular and locally in intragranular microfractures in quartz diorite, amphibolite and chloritized granite of the basement crystalline rocks. The particles consist of major Fe, Cr, and Ni with minor Si and Ca. Origin due to contamination is absolutely ruled out. We believe that these Fe-Cr-Ni particles are probably condensed from the vaporized impacting body which produced the Ries crater. These particles were injected with high velocity into microfractures near the top of the compressed zone, implanted in and across various minerals before these microfractures were resealed. The presence of Si and Ca as well as the fact that the Cr content is nearly twice that of Ni, led us to conclude that the Ries impacting body is very likely not an iron meteorite but a stony meteorite. ?? 1976.

Introduction to the hydrogeochemical investigations within the International Stripa Project

USGS Publications Warehouse

Nordstrom, D. Kirk; Olsson, T.; Carlsson, L.; Fritz, P.

1989-01-01

The International Stripa Project (1980-1990) has sponsored hydrogeochemical investigations at several subsurface drillholes in the granitic portion of an abandoned iron ore mine, central Sweden. The purpose has been to advance our understanding of geochemical processes in crystalline bedrock that may affect the safety assessment of high-level radioactive waste repositories. More than a dozen investigators have collected close to a thousand water and gas samples for chemical and isotopic analyses to develop concepts for the behavior of solutes in a granitic repository environment. The Stripa granite is highly radioactive and has provided an exceptional opportunity to study the behavior of natural radionuclides, especially subsurface production. Extensive microfracturing, low permeability with isolated fracture zones of high permeability, unusual water chemistry, and a typical granitic mineral assemblage with thin veins and fracture coatings of calcite, chlorite, seriate, epidote and quartz characterize the site. Preliminary groundwater flow modeling indicates that the mine has perturbed the flow environment to a depth of about 3 km and may have induced deep groundwaters to flow into the mine. ?? 1989.

Highly oxidising fluids generated during serpentinite breakdown in subduction zones.

PubMed

Debret, B; Sverjensky, D A

2017-09-04

Subduction zones facilitate chemical exchanges between Earth's deep interior and volcanism that affects habitability of the surface environment. Lavas erupted at subduction zones are oxidized and release volatile species. These features may reflect a modification of the oxidation state of the sub-arc mantle by hydrous, oxidizing sulfate and/or carbonate-bearing fluids derived from subducting slabs. But the reason that the fluids are oxidizing has been unclear. Here we use theoretical chemical mass transfer calculations to predict the redox state of fluids generated during serpentinite dehydration. Specifically, the breakdown of antigorite to olivine, enstatite, and chlorite generates fluids with high oxygen fugacities, close to the hematite-magnetite buffer, that can contain significant amounts of sulfate. The migration of these fluids from the slab to the mantle wedge could therefore provide the oxidized source for the genesis of primary arc magmas that release gases to the atmosphere during volcanism. Our results also show that the evolution of oxygen fugacity in serpentinite during subduction is sensitive to the amount of sulfides and potentially metal alloys in bulk rock, possibly producing redox heterogeneities in subducting slabs.

Mineralogy, textures, and relative age relationships of massive sulfide ore in the West Shasta district, California ( USA).

USGS Publications Warehouse

Howe, S.S.

1985-01-01

The Devonian massive sulfide orebodies of the West Shasta district in N California are composed primarily of pyrite, with lesser amounts of other sulfide and gangue minerals. Examination of polished thin sections of more than 100 samples from the Mammoth, Shasta King, Early Bird, Balaklala, Keystone, and Iron Mountain mines suggests that mineralization may be divided into 6 paragenetic stages, the last 5 each separated by an episode of deformation: 1) precipitation of fine-grained, locally colloform and framboidal pyrite and sphalerite; 2) deposition of fine-grained arsenopyrite and coarse-grained pyrite; 3) penetration and local replacement of sulfide minerals of stages 1 and 2 along growth zones and fractures by chalcopyrite, sphalerite, galena, tennantite, pyrrhotite, bornite, and idaite; 4) recrystallization and remobilization of existing minerals; 5) deposition of quartz, white mica, chlorite, and calcite; and 6) formation of bornite, digenite, chalcocite, and covellite during supergene enrichment of several orebodies at the Iron Mountain mine. Mineralogic and textural evidence do not support a second major episode of massive sulfide mineralization during the Permian. -from Author