Experimental Study Assessing the Role of Sedimentary Organic Materials to Control the Redox State of Ground Materials to Control the Redox State of Groundwater: Consumption of Dissolved Oxygen by Humic Acid

Abstract: A total of 189 runs were completed to determine the rate of dissolved oxygen consumption in water by the reaction humic acid at 25°, 45°, and 65°C. Glass vial bottles were used as reaction vessels, and humic aicd and pure water of different intitial O₂ concentration was loaded with humic acid/water weight of 0.008 and 0.009. Vials were opened periodically to measure O₂ concentrations. The pH of the solution fluctuated in the early stages of the experiments and gradually decreased to a constant value. Dissolved oxygen concentration decreased, for example, from initial value of 12 mg/l to 9 mg/l at 25°C, to 5 mg/l at 45°C, and to 2 mg/l at 65°C after the reaction of 500 hours. Analyses of rates suggest that the reaction is first order, and rate constants are 8.42 × 10^-9 at 25°C, 2.22 × 10^-8 at 45°C, and 1.28 × 10^-7 moles m^-2 s^-1 at 65°C.     

乌苏XDR数字化雷达识别雹云指标初探

冰雹是兵团农七师和乌苏市主要灾害性天气之一，常给农业生产造成危害。为了提高防雹作业的效果，1998年对乌苏711雷达进行了数字化改造。作者根据1998～2003年6年回波资料的统计分析，总结出适合本地的识别雹云的指标。     

Late Ediacaran crustal thickening in Iran: Geochemical and isotopic constraints from the ~550 Ma Mishu granitoids (northwest Iran)

The aim of this article is to examine the geochemistry and geochronology of the Cadomian Mishu granites from northwest Iran, in order to elucidate petrogenesis and their role in the evolution of the Cadomian crust of Iran. The Mishu granites mainly consist of two-mica granites associated with scarce outcrops of tonalite, amphibole granodiorite, and diorite. Leucogranitic dikes locally crosscut the Mishu granites. Two-mica granites show S-type characteristics whereas amphibole granodiorite, tonalities, and diorites have I-type signatures. The I-type granites show enrichment in large-ion lithophile elements (e.g. Rb, Ba and K) and depletion in high field strength elements (e.g. Nb, Ti and Ta). These characteristics show that these granites have been formed along an ancient, fossilized subduction zone. The S-type granites have high K, Rb, Cs (and other large ion lithophile elements) contents, resembling collision-related granites. U–Pb zircon dating of the Mishu rocks yielded ²³⁸U/²⁰⁶Pb crystallization ages of ca. 550 Ma. Moreover, Rb–Sr errorchron shows an early Ediacaran age (547 ± 84 Ma) for the Mishu igneous rocks. The two-mica granites (S-type granites) show high ⁸⁷Sr/⁸⁶Sr_(i) ratios, ranging from 0.7068 to 0.7095. Their ?Nd values change between ?4.2 and ?4.6. Amphibole granitoids and diorites (I-type granites) are characterized by relatively low ⁸⁷Sr/⁸⁶Sr_(i) ratios (0.7048–0.7079) and higher values of ?Nd (?0.8 to ?4.2). Leucogranitic dikes have quite juvenile signature, with ?Nd values ranging from +1.1 to +1.4 and Nd model ages (T_DM) from 1.1 to 1.2 Ga. The isotopic data suggests interaction of juvenile, mantle-derived melts with old continental crust to be the main factor for the generation of the Mishu granites. Interaction with older continental crust is also confirmed by the presence of abundant inherited zircon cores. The liquid-line of descend in the Harker diagrams suggests fractional crystallization was also a predominant mechanism during evolution of the Mishu I-type granites. The zircon U–Pb ages, whole rock trace elements, and Sr–Nd isotope data strongly indicate the similarities between the Mishu Cadomian granites with other late Neoproterozoic–early Cambrian (600–520 Ma) granites across Iran and the surrounding areas such as Turkey and Iberia. The generation of the Mishu I-type granites could be related to the subduction of the Proto-Tethyan Ocean during Cadomian orogeny, through interaction between juvenile melts and old (Mesoproterozoic or Archaean) continental crust. The S-type granites are related to the pooling of the basaltic melts within the middle–upper parts of the thick continental crust and then partial melting of that crust.     

Coexisting different types of zoned garnet in kyanite‐quartz eclogites from the Sanbagawa metamorphic belt: Evidence of deformation‐induced lithological mixing during prograde metamorphism

Garnet grains in Sanbagawa quartz eclogites from the Besshi region, central Shikoku commonly show a zoning pattern consisting of core and mantle/rim that formed during two prograde stages of eclogite and subsequent epidote–amphibolite facies metamorphism, respectively. Garnet grains in the quartz eclogites are grouped into four types (I, II, III, and IV) according to the compositional trends of their cores. Type I garnet is most common and sometimes coexists with other types of garnet in a thin section. Type I core formed with epidote and kyanite during the prograde eclogite facies stage. The inner cores of types II and III crystallized within different whole‐rock compositions of epidote‐free and kyanite‐bearing eclogite and epidote‐ and kyanite‐free eclogite at the earlier prograde stage, respectively. The inner core of type IV probably formed during the pre‐eclogite facies stage. The inner cores of types II, III, and IV, which formed under different P–T conditions of prograde metamorphism and/or whole‐rock compositions, were juxtaposed with the core of type I, probably due to tectonic mixing of rocks at various points during the prograde eclogite facies stage. After these processes, they have shared the following same growth history: (i) successive crystal growth during the later stage of prograde eclogite facies metamorphism that formed the margin of the type I core and the outer cores of types II, III, and IV; (ii) partial resorption of the core during exhumation and hydration stage; and (iii) subsequent formation of mantle zones during prograde metamorphism of the epidote–amphibolite facies. The prograde metamorphic reactions may not have progressed under an isochemical condition in some Sanbagawa metamorphic rocks, at least at the hand specimen scale. This interpretation suggests that, in some cases, material interaction promoted by mechanical mixing and fluid‐assisted diffusive mass transfer probably influences mineral reactions and paragenesis of high‐pressure metamorphic rocks.     

Analytical method for stable background reduction for Raman spectra of carbon-containing meteorite and terrestrial samples suffering from intense fluorescence

Chemical states of carbon in terrestrial (meta) sediments and carbonaceous chondrites gather attention as a geothermometer. As a nondestructive analytical method, Raman spectroscopy has been widely used to study their electronic properties, crystallinity, and structural defects through so-called D and G bands. For the analysis of Raman spectra, a common problem is coexistence of a fluorescence background, which should be subtracted prior to the peak-fitting analysis. However, we recently faced a problem that the band shape noticeably changed depending on the background function assumed although the background seemed to be well subtracted at a first glance regardless of the choice of the background function. For the application of the Raman spectroscopy as a geothermometer, a standard background subtraction method must be established to suppress the arbitrariness. In the present study, Raman spectra of seven carbon-containing natural samples, whose background intensities were significantly different, were measured, and their background shape was evaluated by first-, second-, and third-order polynomials. The results indicated that the third-order polynomial was necessary and sufficient as a standard background function. Importantly, although lower order polynomials seem to successfully fit the background at a first glance, they falsely caused dispersion of the shoulder band shape.