Chemical Fluxes of Asian Rivers into Oceans and their Controlling Factors

Chemical fluxes of Asian rivers into oceans bear different regional variations. Three zones are characteristic of distinct dissolved sediment loads and yields and ionic concentration.Rivers into oceans in China play an important role in Asia because of their different chemical fluxes, among which those draining the Loess Plateau have high ionic concentration, low water discharges and dissolved sediment loads and yields.Climate, vegetation, soil and strata lithology, chemical weathering intensity and tectonic activity dominate chemical fluxes of Asian rivers into oceans, and different factors have different effects on the chemical fluxes of separate regional rivers. Rising of the Tibet Plateau also exerts an important influence on chemical compositions of rivers originating from it.     

我国海水制盐工艺改革的设计研究

从技术上和工艺上的可能性、可行性和合理性，论证了海水制盐工艺改革的必要性，并且提出了实现海水制盐工艺改革的各种设计方案。它对我国的海水制盐工业的发展将具有深远意义。     

Geochemical Eccentricity of Ground Water Allied to Weathering of Basalts from the Deccan Volcanic Province,India: Insinuation on CO<Subscript>2</Subscript> Consumption

Analyses of 72 samples from Upper Panjhara basin in the northern part of Deccan Plateau, India, indicate that geochemical incongruity of groundwater is largely a function of mineral composition of the basaltic lithology. Higher proportion of alkaline earth elements to total cations and HCO₃>Cl + SO₄ reflect weathering of primary silicates as chief source of ions. Inputs of Cl, SO₄, and NO₃ are related to rainfall and localized anthropogenic factors. Groundwater from recharge area representing Ca + Mg–HCO₃ type progressively evolves to Ca + Na–HCO₃ and Na–Ca–HCO₃ class along flow direction replicates the role of cation exchange and precipitation processes. While the post-monsoon chemistry is controlled by silicate mineral dissolution + cation exchange reactions, pre-monsoon variability is attributable chiefly to precipitation reactions + anthropogenic factors. Positive correlations between Mg vs HCO₃ and Ca + Mg vs HCO₃ supports selective dissolution of olivine and pyroxene as dominant process in post-monsoon followed by dissolution of plagioclase feldspar and secondary carbonates. The pre-monsoon data however, points toward the dissolution of plagioclase and precipitation of CaCO₃ supported by improved correlation coefficients between Na + Ca vs HCO₃ and negative correlation of Ca vs HCO₃, respectively. It is proposed that the eccentricity in the composition of groundwater from the Panjhara basin is a function of selective dissolution of olivine > pyroxene followed by plagioclase feldspar. The data suggest siallitization (L < R and R _k) as dominant mechanism of chemical weathering of basalts, stimulating monosiallitic (kaolinite) and bisiallitic (montmorillonite) products. The chemical denudation rates for Panjhara basin worked out separately for the ground and surface water component range from 6.98 to 36.65 tons/km²/yr, respectively. The values of the CO₂ consumption rates range between 0.18 × 10⁶ mol//km²/yr (groundwater) and 0.9 × 10⁶ mol/km²/yr (surface water), which indicates that the groundwater forms a considerable fraction of CO₂ consumption, an inference, that is, not taken into contemplation in most of the studies.     

内蒙古正镶白旗碎斑熔岩岩石学特征及其岩相划分

白旗碎斑熔岩为不规则穹状体,可分为边缘玻质碎斑熔岩、过渡霏细碎斑熔岩、中心粒状碎斑熔岩和根部花岗斑岩四个岩性带。从玻质碎斑熔岩到粒状碎斑熔岩,斑晶碎裂度逐渐减弱,珠边结构在粒状碎斑熔岩中最发育,根部花岗斑岩与正常次火山岩相近。碎斑熔岩中钾长石有序度低,指示了岩石高温成因特征。白旌碎斑熔岩属太平洋岩系钙碱质系列,原始岩浆由来源于上地幔和下地壳熔体的混熔作用形成。     

On the role of heat flow, lithosphere thickness and lithosphere density on gravitational potential stresses

Gravitational potential stresses (GPSt) are known to play a first-order role in the state of stress of the Earth's lithosphere. Previous studies focussed mainly on crust elevation and structure and little attention has been paid to modelling GPSt using realistic lithospheric structures. The aim of the present contribution is to quantify gravitational potential energies and stresses associated with stable lithospheric domains. In order to model realistic lithosphere structures, a wide variety of data are considered: surface heat flow, chemical depletion of mantle lithosphere, crustal thickness and elevation. A numerical method is presented which involves classical steady-state heat equations to derive lithosphere thickness, geotherm and density distribution, but additionally requires the studied lithosphere to be isostatically compensated at its base. The impact of varying surface and crustal heat flow, topography, Moho depth and crust density on the signs and magnitudes of predicted GPSt is systematically explored. In clear contrast with what is assumed in most previous studies, modelling results show that the density structure of the mantle lithosphere has a significant impact on the value of the predicted GPSt, in particular in the case of thick lithospheres. Using independent information from the literature, the method was applied to get insights in the state of stress of continental domains with contrasting tectono-thermal ages. The modelling results suggest that in the absence of tectonic stresses Phanerozoic and Proterozoic lithospheres are spontaneously submitted to compression whereas Archean lithospheres are in a neutral to slightly tensile stress state. These findings are in general in good agreement with global stress measurements and observed geoid undulations.     

Platinum and palladium mobility in supergene environment: The residual origin of the Pirogues River mineralization, New Caledonia

Eluvial concentration of platinum-group minerals (PGM) has developed in the south of New Caledonia, from the weathering of a mafic and ultramafic cumulate. The platinum/palladium (Pt/Pd) ratio evolution from the bottom to the top of the weathering profile indicates a chemical mobilization of Pd in supergene environment. The examination by scanning electron microscopy of the residual PGM collected in the weathering profile and their chemical characterization by electronic microprobe show a preservation of the structure and chemical signature (in the core of the grains) of the fresh PGM. This clearly demonstrates that the PGM studied here are residual and are affected by dissolution process.     

Cosmogenic nuclide methods for measuring long-term rates of physical erosion and chemical weathering

Understanding the evolution of geochemical and geomorphic systems requires measurements of long-term rates of physical erosion and chemical weathering. Erosion and weathering rates have traditionally been estimated from measurements of sediment and solute fluxes in streams. However, modern sediment and solute fluxes are often decoupled from long-term rates of erosion and weathering, due to storage or re-mobilization of sediment and solutes upstream from the sampling point. Recently, cosmogenic nuclides such as ¹⁰Be and ²⁶Al have become important new tools for measuring long-term rates of physical erosion and chemical weathering. Cosmogenic nuclides can be used to infer the total denudation flux (the sum of the rates of physical erosion and chemical weathering) in actively eroding terrain. Here we review recent work showing how this total denudation flux can be partitioned into its physical and chemical components, using the enrichment of insoluble tracers (such as Zr) in regolith relative to parent rock. By combining cosmogenic nuclide measurements with the bulk elemental composition of rock and soil, geochemists can measure rates of physical erosion and chemical weathering over 1000- to 10,000-year time scales.     

Airborne gamma-ray spectrometry to quantify chemical erosion processes

Airborne gamma-ray spectrometry data (uranium, potassium and thorium contents) reveal geochemical heterogeneities within the monolithological Hyrôme watershed (ca. 150 km²) in the Armorican massif (western France). Our observations and computations provide important constraints on the spatial distribution and the associated magnitudes of chemical erosion processes at the scale of a small watershed. Two distinct, partially preserved, weathering profiles exhibit a strong correlation between regolith evolution and airborne-derived K/Th ratios, suggesting that the variability is linked to supergene processes. Using both airborne data and laboratory measurements on rock samples, the total net export of potassium has been estimated at 422 ± 50 kg/m² and the chemical weathering rate of potassium at 17 ± 2 kg/km²/a.     

Forests, climate, and silicate rock weathering

Over time periods of 10⁶ years and longer, atmospheric carbon dioxide content is largely controlled by a balance between silicate rock weathering and CO₂ sources (degassing from the Earth plus net organic carbon oxidation). Vegetation cover can affect silicate rock weathering rates by increasing soil CO₂ content, stabilizing soil cover, and producing organic acids. Forests absorb more solar radiation than most other ecosystems; this tends to warm Earth's climate, especially outside of the tropics; this warmth would tend to increase silicate rock weathering rates. Here, we develop preliminary parameterizations of this effect that could be incorporated into carbonate–silicate cycle models, based on the results of general circulation model simulations.     

Genesis of monazite and Y zoning in garnet from the Black Hills, South Dakota

The paragenesis of monazite in metapelitic rocks from the contact aureole of the Harney Peak Granite, Black Hills, South Dakota, was investigated using zoning patterns of monazite and garnet, electron microprobe dating of monazite, bulk-rock compositions, and major phase mineral equilibria. The area is characterized by low-pressure and high-temperature metamorphism with metamorphic zones ranging from garnet to sillimanite zones. Garnet porphyroblasts containing euhedral Y annuli are observed from the garnet to sillimanite zones. Although major phase mineral equilibria predict resorption of garnet at the staurolite isograd and regrowth at the andalusite isograd, textural and mass balance analyses suggest that the formation of the Y annuli is not related to the resorption-and-regrowth of garnet having formed instead during garnet growth in the garnet zone. Monazite grains in Black Hills pelites were divided into two generations on the basis of zoning patterns of Y and U: monazite 1 with low-Y and -U and monazite 2 with high-Y and -U. Monazite 1 occurs in the garnet zone and persists into the sillimanite zone as cores shielded by monazite 2 which starts to form in the andalusite zone. Pelites containing garnet porphyroblasts with Y annuli and monazite 1 with patchy Th zoning are more calcic than those with garnet with no Y annuli and monazite with concentric Th zoning. Monazite 1 is attributed to breakdown of allanite in the garnet zone, additionally giving rise to the Y annuli observed in garnet. Monazite 2 grows in the andalusite zone, probably at the expense of garnet and monazite 1 in the andalusite and sillimanite zones. The ages of the two different generations of monazite are within the precision of chemical dating of electron microprobe. The electron microprobe ages of all monazites from the Black Hills show a single ca. 1713 Ma population, close to the intrusion age of the Harney Peak Granite (1715 Ma). This study demonstrates that Y zoning in garnet and monazite are critical to the interpretation of monazite petrogenesis and therefore monazite ages.