Magmatic and hydrothermal R.E.E. fractionation in the Xihuashan granites (SE China)

The Xihuashan stock (South Jiangxi, China) is composed of cogenetic granitic units (granites Xe, a, c, d and b) and emplaced during the Yanshanian orogeny (153±0.2 Ma). They are two feldspars, Fe-rich biotite±garnet and slightly peraluminous granites. Primary accessory minerals are apatite 1, monazite, zircon, uranothorite±xenotime in granites Xe and a, zircon, uranothorite, uraninite, betafite, xenotime 1; hydrothermal minerals are monazite altered into parisite and apatite 2, Y-rich parisite, yttroparisite, Y-rich fluorite and xenotime 2 in granites c and b. Petrographic observations, major element, REE, Y and Rb–Sr isotropic data point to a magmatic suite (granites Xe and a granites c and d granite b) distinct from hydrothermal Na-or K-alteration of b. From granite Xe to granite b, LREE, Eu, Th and Zr content are strongly depleted, while HREE, Y and U content increase. During K-alteration of b, these variations are of minor importance. Major and accessory mineral evidences, geochemical and fluid inclusion results indicate two successive alteration fluids interacting with b, (1) a late-magmatic F^– and CO₂–rich fluid and (2) a post-magmatic, aqueous and slightly saline fluid. The depletion of LREE and Th content and the increase in HREE, Y and U content correspond, in the magmatic suite to the early fractionation of monazite in the granites where there is no hydrothermal alteration (granites Xe and e) and to the hydrothermal alteration of monazite into parisite and secondary apatite, intense new formation of yttroparisite, Y enrichment and U loss in the uranothorite and late crystallization of uraninite in the granites c and b. Moreover, simulated crystallization of monazite and temperature of monazite saturation show early fractionation of monazite from the magma in the less evolved granites (Xe and e) and prevailing hydrothermal leaching of monazite in the most evolved granites (c-d and b) related to a late-magmetic event. The slight variations of REE, Y, Th and U content in the K-altered granites compared to granite b emphazes the distinct chemical nature of the successive hydrothermal fluids. Rb–Sr and Sm–Nd isotopic results point to a 30 Ma period of time between the late-magmatic and the post-magmatic fluid circulation.     

Contribution of E.S.R. analysis toward diagenic mechanisms in bituminous deposits

The E.S.R. g-values of a variety of bituminous materials have been plotted against a function of their heteroatom content ∑δ_κX_κ, where δ is the splitting coefficient of the given heteroatom κ, and X is its atomic fraction. Three discrete series are evident: two coal series, one exhibiting direct variation of g with ∑δ_κX_κ (Series I), the other exhibiting an inverse relationship (Series II). The petroleum asphaltenes, as well as most asphaltites and asphaltoids (Series III), lie above and roughly parallel to Series I. Sulfur-treated asphaltics approach Series I, whereas heated asphaltenes and resins are situated around the intersection of Series II and III.Bituminous deposits may transform through diagenesis to their mature forms, as evidenced by their increase in the delocalization (increased aromaticity) with a decrease in heteroatom content. The diagenesis of coal is reliant on oxygen whose elimination may result in aromatization (Series I), and further transformations may increase active peripheral oxygen function groups (Series II). The intersection of Series I and II contains the delocalization states. There exist major differences in the precursors and mode of transformation between members of the coal and asphaltene series.     

Magmatic fluids in the Fen carbonatite complex,S.E. Norway

Three different types of carbonatite magma may be recognized in the Cambrian Fen complex, S.E. Norway: (1) Peralkaline calcite carbonatite magma derived from ijolitic magma; (2) Alkaline magnesian calcite carbonatite magma which yielded biotite-amphibole søvite and dolomite carbonatite; and (3) ferrocarbonatite liquids, related to (2) and/or to alkaline lamprophyre magma (damjernite). Apatite formed during the pre-emplacement evolution of (2) contains inclusions of calcite and dolomite, devitrified mafic silicate glass and aqueous fluid. All of these inclusions have a magmatic origin, and were trapped during a mid-crustal fractionation event (P4 kbars, T625° C), where apatite and carbonates precipitated from a carbonatite magma which coexisted with a mafic silicate melt. The fluid inclusions contain water, dissolved ionic species (mainly NaCl, with minor polyvalent metal salts) and in some cases CO₂. Two main groups of fluid inclusions are recognized: Type A: CO₂-bearing inclusions, of approximate molar composition H2O _88–90 CO _27-5 NaCl ₅ (d=0.85–0.87 g/ cm³). Type B: CO₂-free aqueous inclusions with salinities from 1 to 24 wt% NaCl_eq and densities betwen 0.7 and 1.0 g/cm³. More strongly saline type B inclusions (salinity ca. 35wt%, d=1.0 to 1.1 g/cm³) contain solid halite at room temperature and occur in overgrowths on apatite. Type A inclusions probably contain the most primitive fluid, from which type B fluids have evolved during fractionation of the magmatic system. Type B inclusions define a continuous trend from low towards higher salinities and densities and formed as a result of cooling and partitioning of alkali chloride components in the carbonatite system into the fluid phase. Available petrological data on the carbonatites show that the fluid evolution in the Fen complex leads from a regime dominated by juvenile CO₂ + H₂O fluids during the magmatic stage, to groundwater-derived aqueous fluids during post-magmatic reequilibration.     

Meteoric water-basalt interactions. II: A field study in N.E. Iceland

The compositions of rain, snow, melt, spring and geothermal waters from the rift zone of N.E. Iceland can be explained by seaspray addition, chemical fractionation at the seawater-air interface, burning of fossil fuel, farming activities, purification by partial melting of snow and ice, dissolution of basalts and buffering by alteration minerals. The dissolution of the rocks appears to be incongruent. During solute acquisition, spring compositions move through the stability fields of kaolinite and smectite to the laumontite and illite fields. All but four of the springs are undersaturated with respect to calcite. Silica concentrations are compatible with the solubility of basaltic glass. The reactions reflected in the spring waters appear to have taken place sealed off from atmospheric CO₂ after initial saturation.The geothermal waters which are recharged by the spring waters are depleted in Mg and Ca but enriched in carbon and sulfur with respect to dissolution of primary rocks. Expressions are derived relating dissolution rates of rocks, age of groundwaters, physical properties of groundwaters and mass transfer. The characteristic rock particle radii in the cold water aquifers range from 0.2 to 2 cm and the characteristic crack openings are of the order 0.04 to 0.4 cm. Using laboratory studies on the Icelandic lavas as a guide, the residence times of the cold waters in the aquifers can be estimated at 60 days to 4 years. The average active surface area of the aquifers enclosing 1000 g of spring water is of the order of 0.6 to 6 m² and these 1000 g of water have reacted with 0.1 to 1 g of basaltic rocks. The same mass of thermal water has interacted with 100 to 300 g of unaltered rocks.     

THE LATE CENOZOIC FORMATIONS OF S.E.SHANSI

Up to 1931 nothing was positively known concerning the Cenozoicformations eventually preserved in S.E.Shansi.The large area bounded by