The grain‐scale spatial arrangement of melt in layer‐parallel leucosomes in two anatectic rocks from two different contact aureoles located in central Maine, USA, is documented and used to constrain the controls on grain‐scale melt localization. The spatial distribution of grain‐scale melt is inferred from microstructural criteria for recognition of mineral pseudomorphs after melt and mineral grains of the solid matrix that hosted the melt. In both rocks, feldspar mimics the grain‐scale distribution of melt, and quartz is the major constituent of the solid matrix. The feldspar pockets consist of individual feldspar grains or aggregates of feldspar grains that show cuspate outlines. They have low average width/length ratios (0.54 and 0.55, respectively), and are interstitial between more rounded and equant (width/length ratios 0.65 for both samples) quartz grains. In two dimensions, the feldspar pockets extend over distances equivalent to multiple quartz grain diameters, possibly forming a connected three‐dimensional intergranular network. Both samples show similar mesoscopic structural elements and in both samples the feldspar pockets have a shape‐preferred orientation. In one sample, feldspar inferred to replace melt is aligned subparallel to the shape‐preferred orientation of quartz, indicating that pre‐ or syn‐anatectic strain controlled the grain‐scale distribution of melt. In the other sample, the preferred orientation of feldspar inferred to replace melt is different from the orientations of all other mesoscopic or microscopic structures in the rock, indicating that differential stress controlled grain‐scale melt localization. This is probably facilitated by conditions of higher differential stress, which may have promoted microfracturing. Grain‐scale melt distribution and inferred melt localization controls give insight into possible grain‐scale deformation mechanisms in melt‐bearing rocks. Application of these results to the interpretation of deep crustal anatectic rocks suggests that grain‐scale melt distribution should be controlled primarily by pre‐ or syn‐anatectic deformation. Feedback relations between melt localization and deformation are to be expected, with important implications for deformation and tectonic evolution of melt‐bearing rocks. 相似文献
A decrease in temperature (ΔT up to 45.5 °C) and chloride concentration (ΔCl up to 4.65 mol/l) characterises the brine–seawater boundary in the Atlantis-II, Discovery, and Kebrit Deeps of the Red Sea, where redox conditions change from anoxic to oxic over a boundary layer several meters thick. High-resolution (100 cm) profiles of the methane concentration, stable carbon isotope ratio of methane, and redox-sensitive tracers (O2, Mn4+/Mn2+, Fe3+/Fe2+, and SO42−) were measured across the brine–seawater boundary layer to investigate methane fluxes and secondary methane oxidation processes.
Substantial amounts of thermogenic hydrocarbons are found in the deep brines (mostly methane, with a maximum concentration up to 4.8×105 nmol/l), and steep methane concentration gradients mainly controlled by diffusive flow characterize the brine–seawater boundary (maximum of 2×105 nmol/l/m in Kebrit Deep). However, locally the actual methane concentration profiles deviate from theoretical diffusion-controlled concentration profiles and extremely positive δ13C–CH4 values can be found (up to +49‰ PDB in the Discovery Deep). Both, the actual CH4 concentration profiles and the carbon-13 enrichment in the residual CH4 of the Atlantis-II and Discovery Deeps indicate consumption (oxidation) of 12C-rich CH4 under suboxic conditions (probably utilizing readily available—up to 2000 μmol/l—Mn(IV)-oxihydroxides as electron acceptor). Thus, a combined diffusion–oxidation model was used to calculate methane fluxes of 0.3–393 kg/year across the brine–seawater boundary layer. Assuming steady-state conditions, this slow loss of methane from the brines into the Red Sea bottom water reflects a low thermogenic hydrocarbon input into the deep brines. 相似文献
A laboratory study was carried out to investigate the secondary organic aerosol products from photooxidation of the aromatic hydrocarbon toluene. The laboratory experiments consisted of irradiating toluene/propylene/NOx/air mixtures in a smog chamber operated inthe dynamic mode and collecting submicron secondary organic aerosol samples through a sampling train that consisted of an XAD denuder and a ZefluorTM filter. Oxidation products in the filter extracts were treated using O-(2,3,4,5,6,-pentafluorobenzyl)-hydroxylamine (PFBHA) to derivatize carbonyl groups followed by treatment with N,O-Bis(trimethylsilyl)-acetamide (BSTFA) to derivatize OH groups. The derivatized products were detected with a positive chemical ionization (CI) gas chromatography ion trap mass spectroscopy (GC-ITMS) system. The results of the GC-ITMS analyses were consistent with the previous studies that demonstrated the formation of multi-functional oxygenates. Denuder results showed that many of these same compounds were present in the gas, as well as, the particle phase. Moreover, evidence was found for a series of multifunctional acids produced as higher order oxidation products of the toluene/NOx system. Products having nearly the same mass spectrumwere also found in the ambient environment using identical analytical techniques. These products having multiple acid and alcoholic-OH moieties have substantially lower volatility than previously reported SOA products of the toluene photooxidation and might serve as an indicator for aromatic oxidation in the ambient atmosphere. 相似文献
The geochemical evolution of two acid mine effluents in Tharsis and La Zarza-Perrunal mines (Iberian Pyrite Belt, Huelva, Spain) has been investigated. In origin, these waters present a low pH (2.2 and 3.1) and high concentrations of dissolved sulphate and metals (Fe, Al, Mn, Cu, Zn, As, Cd, Co, Cr, Ni). However, the natural evolution of these acidic waters (which includes the bacterial oxidation of Fe(II) and the subsequent precipitation of Fe(III) minerals) represents an efficient mechanism of attenuation. This self-mitigating process is evidenced by the formation of schwertmannite, which retains most of the iron load and, by sorption, toxic trace elements like As. The later mixing with pristine waters rises the pH and favours the total precipitation of Fe(III) at pH 3.5 and, subsequently, Al compounds at pH 4.5, along with the sorption of trace metals (Mn, Zn, Cu, Cd, Co, Ni) until chemical equilibrium at circumneutral conditions is achieved. 相似文献
1 Geological Setting making the southern margin of Turpan-Hami basin one of the important uranium-productive regions of interlayer The Turpan-Hami basin is one of the three greatest basins oxidation type sandstone-hosted uranium deposits inin the Xinjiang Uygur Autonomous Region. It is located in China. Up to now, the large-scale Shihongtan uraniumthe Junggar-Turpan microplate at the southeastern end of deposit and some uranium ore occurrences have beenthe Kazakhstan-Junggar plate. The b… 相似文献
Abstract. Many granitic plutons of Early Cretaceous age are intruded on various scales in the Kitakami Mountains. The stock‐type Ganidake pluton accompanies enormous Fe‐Cu mineralization of the Kamaishi deposits, whereas the Kurihashi pluton accompanies less mineralization. To elucidate the cause of these differences, the metamorphic conditions and redox state of the contact metamorphic aureole around the Kurihashi pluton have been examined by the petrochemical study and gas analysis of the metamorphic rocks. A typical mineral assemblage in the pelitic rocks in the lowest‐grade part is biotite‐muscovite‐chlorite‐quartz‐plagio‐clase‐graphite, which occur more than 2 km away from the contact point with the Kurihashi pluton. Graphite disappears at the 1550 m point, and cordierite and garnet appear in the middle and highest‐grade parts, respectively. A typical mineral assemblage in the tuffaceous rocks in the lower‐grade part is chlorite‐actinolite‐biotite‐quartz‐plagioclase. Actinolite changes into hornblende near to the pluton. The CO2/CH4 ratios obtained in measurements by gas chromatography exceeds 100 in the pelitic rocks at the contact point with the pluton. The ratios decrease and become less than 0.1 with distance from the pluton. Equilibrium temperatures calculated from a garnet‐biotite pair in the pelitic rock and a hornblende‐plagioclase pair in the tuffaceous rock are 640d? and 681 d?C at the contact point, respectively. The log?o2 values among these metamorphic aureoles estimated from the CO2/CH4 ratios are slightly lower than the FMQ‐buffer. Redox states of the contact metamorphic aureole are kept in an intermediate condition between oxidized magma of the Kurihashi pluton and graphite‐bearing pelitic country rocks. Judging from these metamorphic conditions around the Kurihashi pluton and from the re‐evaluation of the previous knowledge about contact metasomatism around the Ganidake pluton, the Kurihashi metamorphism has occurred at higher temperatures and dry conditions than the Ganidake metasomatism. These differences in the metamorphic conditions and presence or absence of a large limestone mass around the pluton might be the principal reasons why the Kurihashi pluton accompanies less mineralization and the Ganidake pluton accompanies gigantic Kamaishi skarn mineralization. 相似文献