The peterson limestone — early cretaceous lacustrine carbonate deposition in western wyoming and southeastern idaho

The lacustrine Peterson Limestone of western Wyoming and southeastern Idaho comprises six lithofacies throughout its 20,000 km² aerial extent. These are: (1) calcareous sandstone and shale, (2) red nodular limestone, (3) pink sandy micrite, (4) biomicrite, (5) graded silty micrite, and (6) limestone conglomerate. The first two represent floodplain deposition and paleosols, whereas the remaining are shallow nearshore and deeper lacustrine sediments.This sequence was developed in a large fresh, hardwater lake surrounded by fluvial systems and associated flood plains in a warm temperate climate. Well-oxidized sandy terrigenous rocks, together with calcareous paleosol nodules, indicate that flood-plain deposition both preceded and was concurrent with lacustrine carbonate deposition. Micrite and biomicrite formed in deeper parts of the basin while sandy and silty carbonate accumulated in shallower lake-margin areas. Less-calcareous shale units which are interbedded with deeper-water carbonate were deposited either during rapid basin subsidence and deepening of the lake center or during periods of slower carbonate precipitation. Turbidity currents and subaqueous debris flows generated along steeper lake margins, resulted in the deposition of rhythmic layers of graded silty micrite and diamictic limestone conglomerate in the deepest part of the basin. The carbonate-rich sediments comprising these two lithofacies were originally deposited on shallow lake-margin benches and subsequently were transported downslope toward the lake center.Comparison with other carbonate-precipitating lacustrine systems indicates that this lake was not like modern playas. Although no known modern lacustrine system is precisely like Lake Peterson, the flora, fauna, composition, and distribution of facies within modern temperate-region lakes most closely resemble those of the Peterson Limestone.     

Mo isotope fractionation during adsorption to Fe (oxyhydr)oxides

Molybdenum (Mo) isotopes have great potential as a paleoredox indicator, but this potential is currently restricted by an incomplete understanding of isotope fractionations occurring during key (bio)geochemical processes. To address one such uncertainty we have investigated the isotopic fractionation of Mo during adsorption to a range of Fe (oxyhydr)oxides, under variable Mo/Fe-mineral ratios and pH. Our data confirm that Fe (oxyhydr)oxides can readily adsorb Mo, highlighting the potential importance of this removal pathway for the global Mo cycle. Furthermore, adsorption of Mo to Fe (oxyhydr)oxides is associated with preferential uptake of the lighter Mo isotopes. Fractionations between the solid and dissolved phase (Δ⁹⁸Mo) increase at higher pH, and also vary with mineralogy, increasing in the order magnetite (Δ⁹⁸Mo = 0.83 ± 0.60‰) < ferrihydrite (Δ⁹⁸Mo = 1.11 ± 0.15‰) < goethite (Δ⁹⁸Mo = 1.40 ± 0.48‰) < hematite (Δ⁹⁸Mo = 2.19 ± 0.54‰). Small differences in isotopic fractionation are also seen at varying Mo/Fe-mineral ratios for individual minerals. The observed isotopic behaviour is consistent with both fractionation during adsorption to the mineral surface (a function of vibrational energy) and adsorption of different Mo species/structures from solution. The different fractionation factors determined for different Fe (oxyhydr)oxides suggests that these minerals likely exert a major control on observed natural Mo isotope compositions during sediment deposition beneath suboxic through to anoxic (but non-sulfidic) bottom waters. Our results confirm that Mo isotopes can provide important information on the spatial extent of different paleoredox conditions, providing they are used in combination with other techniques for evaluating the local redox environment and the mineralogy of the depositing sediments.     

Ordovician eclogites from the Chinese Beishan: implications for the tectonic evolution of the southern Altaids

Numerous lenses of eclogite occur in a belt of augen orthogneisses in the Gubaoquan area in the southern Beishan orogen, an eastern extension of the Tianshan orogen. With detailed petrological data and phase relations, modelled in the system NCFMASHTO with thermocalc , a quantitative P–T path was estimated and defined a clockwise P–T path that showed a near isothermal decompression from eclogite facies (>15.5 kbar, 700–800 °C, omphacite + garnet) to high‐pressure granulite facies (12–14 kbar, 700–750 °C, clinopyroxene + sodic plagioclase symplectitic intergrowths around omphacite), low‐pressure granulite facies (8–9.5 kbar, ～700 °C, orthopyroxene + clinopyroxene + plagioclase symplectites and coronas surrounding garnet) and amphibolite facies (5–7 kbar, 600–700 °C, hornblende + plagioclase symplectites). The major and trace elements and Sm–Nd isotopic data suggest that most of the Beishan eclogite samples had a protolith of oceanic crust with geochemical characteristics of an enriched or normal mid‐ocean ridge basalt. The U–Pb dating of the Beishan eclogites indicates an Ordovician age of c. 467 Ma for the eclogite facies metamorphism. An ³⁹Ar/⁴⁰Ar age of c. 430 Ma for biotite from the augen gneiss corresponds to the time of retrograde metamorphism. The combined data from geological setting, bulk composition, clockwise P–T path and geochronology support a model in which the Beishan eclogites started as oceanic crust in the Palaeoasian Ocean, which was subducted to eclogite depths in the Ordovician and exhumed in the Silurian. The eclogite‐bearing gneiss belt marks the position of a high‐pressure Ordovician suture zone, and the calculated clockwise P–T path defines the progression from subduction to exhumation.     

Enhanced bioremoval of refractory compounds from dyeing wastewater using optimized sequential anaerobic/aerobic process

The upflow anaerobic sludge blanket process followed by the biological aerated filter process was employed to improve the removal of color and recalcitrant compounds from real dyeing wastewater. The highest removal efficiency for color was observed in the anaerobic process, at 8-h hydraulic retention time, seeded with the sludge granule. In the subsequent aerobic process packed with the microbe-immobilized polyethylene glycol media, the removal efficiency for chemical oxygen demand increased significantly to 75 %, regardless of the empty bed contact time. The average influent non-biodegradable soluble chemical oxygen demand was 517 mg/L, and the average concentration in effluent from the anaerobic reactor was 363 mg/L, suggesting the removal of some recalcitrant matters together with the degradable ones. The average non-biodegradable soluble chemical oxygen demand in effluent from the aerobic reactor was 87, 93, and 118 mg/L, with the removal efficiency of 76, 74, and 67 %, at 24-, 12-, and 8-h empty bed contact time, respectively. The combined anaerobic sludge blanket and aerobic cell-entrapped process was effective to remove the refractory compounds from real dyeing wastewater as well as in reducing organic loading to meet the effluent discharge limits. This integrated process is considered an effective and economical treatment technology for dyeing wastewater.     

Isotopic constraints on Columbia River flood basalt genesis and the nature of the subcontinental mantle

Pb, O, Nd, and Sr isotopic data for the Columbia River basalts paint a complex picture for the origin of this flood basalt province. At least 3 distinct mantle sources appear to have been involved, superimposed upon which are the effects of crystal fractionation and mass exchange with evolved crustal wallrocks. To a large degree, the initiation of Columbia River volcanism and the geochemical characteristics of the basalts appear to have been influenced by subduction of the Juan de Fuca plate beneath the North American plate in a manner analogous to the origin of back-arc basins. The physical structure of the crust appears to have influenced the late stage evolution of the magmas by directing the locus of eruption to the border between the ancient continental interior and much younger crust to the south and west. This proximity to the continental interior also allowed old enriched subcontinental mantle to become involved in the very late stages of Columbia River volcanism. An important consequence of the existence of enriched mantle regions beneath continents is that the combination, crust plus enriched mantle, requires more incompatible elements to have been extracted from the remainder of the mantle than would be the case if no enriched mantle existed.     

Function of a deltaic silt deposit as a repository and long-term source of sulfate and related weathering products in a glaciofluvial aquifer derived from organic-rich shale (North Dakota,USA)

A shallow unconfined glaciofluvial aquifer in North Dakota (USA) has largest groundwater sulfate concentrations near the bottom boundary. A deltaic silt layer underlying the aquifer, at >16 m, is the modern proximate sulfate source for the aquifer. The original sulfate source was pyrite in the organic-rich shale component of the aquifer and silt grain matrix. An oxidizing event occurred during which grain-matrix pyrite sulfur was oxidized to sulfate. Thereafter the silt served as a “conserving” layer, slowly feeding sulfate into the lower part of the aquifer and the underlying till. A method was developed for estimating the approximate initial sulfate concentration in the source layer and the redistribution time since the oxidizing event, using a semi-generic convection–dispersion model. The convection–dispersion model and a model for the evolution of modern sulfate δ ³⁴S in silt-layer pore water from the initial grain-matrix pyrite δ ³⁴S, both estimated that the oxidizing event occurred several thousand years ago, and was likely related to the dry conditions of the Hypsithermal Interval. The silt layer also serves as an arsenic source. Results indicate that deltaic silts derived from organic-rich shale parent materials in a glacial environment can provide long-term sources for sulfate and arsenic and possibly other related oxidative weathering products.     

Cumberland Falls chondritic inclusions: Mineralogy/petrology of a forsterite chondrite suite

As previously found for a chondritic inclusion of unknown affinity, mineralogic and petrologic properties of 9 inclusions in the Cumberland Falls enstatitc achondrite are primitive members of the forsterite (F) chondrite group, hitherto defined by 4 meteorites of similar redox state. The inclusions define a primitive suite with properties indicating 8 as F3 and one of even lower petrologic type. The abundant minerals include: low-Ca pyroxene, olivine, plagioclase, kamacite, taenite, schreibersite, troilite, ferroan alabandite and daubreelite. Diopside, oldhamite and a Ti-rich sulfide are present in one or two inclusions. Petrologic textures and jadeitic pyroxene, hitherto unidentified in meteorites, indicate substantial degree of shock. The inclusions acquired their chemical characteristics during nebular condensation and accretion over a broad redox range (metal-silicate trends in them verify Prior's Rules): their parent body later impacted the enstatite meteorite parent body. During impact, the inclusions were shocked and incorporated with enstatite achondrite host as a breccia that would become Cumberland Falls.     

Kinetic and equilibrium study of Ni(II) sorption from aqueous solutions onto Peganum harmala-L

In this study, the adsorption behavior of Ni(II) in an aqueous solution system using natural adsorbent Peganum harmala-L was measured via batch mode. The prepared sorbent was characterized by scanning electron microscope, Fourier transform infrared spectroscopy, N₂ adsorption–desorption and pH_zpc. Adsorption experiments were carried out by varying several conditions such as contact time, metal ion concentration and pH to assess kinetic and equilibrium parameters. The equilibrium data were analyzed based on the Langmuir, Freundlich, Temkin and Dubinin–Radushkevich isotherms. Kinetic data were analyzed using the pseudo-first-order, pseudo-second-order and intra-particular diffusion models. Experimental data showed that at contact time 60 min, metal ion concentration 50 mg/L and pH 6, a maximum amount of Ni(II) ions can be removed. The experimental data were best described by the Langmuir isotherm model as is evident from the high R ² value of 0.988. The adsorption capacity (q _m) obtained was 68.02 mg/g at an initial pH of 6 and a temperature of 25 °C. Kinetic studies of the adsorption showed that equilibrium was reached within 60 min of contact and the adsorption process followed the pseudo-first-order model. The obtained results show that P. harmala-L can be used as an effective and a natural low-cost adsorbent for the removal of Ni(II) from aqueous solutions.     

Low molecular weight polyacrylamide-based polymers as modifiers in phosphate beneficiation

The phosphate industry currently uses several natural polymers such as starch and guar as modifiers to achieve better separation of phosphate from silicates and carbonates. These natural products have many drawbacks: poor selectivity, low performance/dosage ratio, instability and sensitivity to aging, batch variability in composition, and deleterious down-stream effects. Several new, synthetic, low molecular weight polymers have recently been developed as cost-effective alternatives to natural products. These polymers have not only overcome many of the problems associated with natural products, but also have high activity and selectivity.The approach used in designing the synthetic polymers was to incorporate functional groups that would adsorb selectively on the mineral surface thereby rendering it hydrophilic. The phosphate modifier (depressant) developed recently is a low molecular weight polyacrylamide containing both hydroxyl and carboxylic acid functional groups. This polymer has provided excellent selectivity in the separation of apatite from siliceous gangue. The role of this and related polymers in the selective cationic flotation of quartz from apatite is discussed in this paper. The structure-activity relationships have been studied by determining the modifier activity of a range of polyacrylamides containing hydroxyl, carboxyl or carboxymethylol groups.     

Stability of Yoderite in the Absence and in the Presence of Quartz: an Experimental Study in the System MgO-Al2O3-Fe2O3-SiO2-H2O

The water-pressure temperature stability field of yoderite,ideally Mg₂Al_5.6Fe^{3 +} _0.4Si₄O₁₈(OH)₂, was determined at highoxygen fugacities by high-pressure bracketing runs on eightpossible breakdown reactions involving the phases chlorite,kyanite, talc, staurolite, pyrope, enstatite, boron-free kornerupine,cordierite, quartz, and invariably an excess of hematite. Yoderitewas found to be stable over the surprisingly large PT rangefrom 6 to 25 kbar water pressure and 590 to 795 C. It is thusa high-pressure mineral covering the upper amphibolite and portionsof the eclogite facies. In the presence of quartz its upperpressure stability is reduced to some 15 kbar, and its uppertemperature stability to 715 C. Two of the yoderite-producingreactions are anomalous as they show dehydration in the directiontowards lower temperatures. Importantly, this is also true forthe reaction kyanite + talc + hematite+H₂O=yoderite+quartz whichis responsible for the only yoderite occurrence in nature atMautia Hill, Tanzania. Preliminary thermodynamic calculationsindicate that—owing to this unusual dehydration behavior—thestability field for the assemblage yoderite+quartz disappearsfor water activities lower than 0.5. The rarity of yoderitein natural rocks, which is in contrast to its large PT stabilityfield, must be explained on chemical rather than on physicalgrounds. Yoderite can only occur in whiteschist-type bulk compositionsrich in MgO, Al₂O₃, SiO₂, and containing some iron, but poorin alkalis and CaO. Oxygen fugacities must be unusually highto keep Fe trivalent, and—at least for rocks with excessquartz—the water activity must be high as well. In anenvironment of this kind, yoderite formation in the Mautia Hillwhiteschist may have occurred even at constant total pressureand temperature simply by an influx of hydrous fluid duringthe late stages of metamorphism under amphibolite facies conditions.