Miscellaneous information 1989 (Addendum)

Miscellaneous information 1989 (Addendum)     

柴达木盆地北缘大柴旦地区古生代花岗岩锆石SHRIMP定年

大柴旦地区是柴北缘古生代超高压带的重要组成部分,与超高压岩石相伴的花岗岩十分发育。这些花岗岩具有两类不同的岩石地球化学特征,Ⅰ类以 Na_2O/K_2O 比值小于1、明显的负 Eu 异常和低 Sr、高 Y 为特征,具有 S-型花岗岩的属性,Ⅱ类以 Na_2O/K_2O 比值大于1、弱负 Eu 异常到正 Eu 异常和高 Sr、低 Y 为特征,具有Ⅰ-型花岗岩的属性,反映了它们的源岩及成因上的差异。锆石 SHRIMP U—Ph 定年结果表明,大柴旦地区花岗岩的年龄可分为三组,第一组年龄为446.3±3.9Ma,第二组年龄分别为408.6±4.4Ma、403.3±3.8Ma、401.8±3Ma,第三组年龄分别为374.5±1.6Ma、372±2.1Ma。结合区域地质特征,我们认为,第一组年龄可能反映了柴达木陆块与中南祁连板块碰撞的时代,第二组年龄可能反映了深俯冲地下的板块由于拆沉而折返的时代,第三组年龄可能反映了碰撞隆起后造山带上不同块体之间的伸展、滑塌的时代。     

Decolorisation of exhausted reactive dye bath using ozonator for reuse

Exhausted Reactive dye bath samples of Turquoise Blue, Olive Green and Navy Blue shades were collected from cotton knit wear dyeing units in Tirupur. Ozonation was conducted in a column reactor system fed with ozone at the rate of 0.16 g/min to assess its efficiency in reducing the color, chemical oxygen demand and total organic carbon. Complete decolorization of the effluent was achieved in 10 min contact time and ozone consumption of 153 mg/ L for Turquoise Blue, 128 for Olive Green and 143 for Navy Blue shades effluents respectively. The corresponding COD removal was 43%, 44% and 43% for the three shades while TOC removal efficiency was 45%, 45% and 40% respectively. The results from the reusability studies indicate that the dyeing quality was not affected by the reuse of decolorized dye bath for two successive cycles. It is concluded that ozonation is efficient in decolorization of exhausted dye bath effluents containing conventional reactive dyes. However, the corresponding removal of COD from the textile effluent was not significant.     

The Geochemistry of Lake Joyce, McMurdo Dry Valleys, Antarctica

Lake Joyce is one of the least studied lakes of the McMurdo Dry Valleys. Similar to other lakes in this region, Lake Joyce is a closed-basin, permanently ice-covered, meromictic lake. We present here a detailed investigation of major ions, nutrients, and dissolved trace elements for Lake Joyce. Specifically, we investigate the role of iron and manganese oxides and hydrous oxides in trace metal cycling.Lake Joyce is characterized by fresh, oxic waters overlying an anoxic brine, primarily Na–Cl. Surface waters have a maximum nitrate concentration of 26M with a molar dissolved inorganic nitrogen to phosphorus ratio of 477. The supply of nitrogen is attributed to atmospheric deposition, possibly from polar stratospheric clouds. Dissolved phosphorus is scavenged by hydrous iron oxides. The pH is highest (10.15) just beneath the 7-m thick ice cover and decreases to a minimum of 7.29 in the redox transition zone. Dissolved Al exceeds 8M in surface waters, and appears to be controlled by equilibrium with gibbsite. In contrast, concentrations of other trace elements in surface waters are quite low (e.g., 5.4nM Cu, 0.19nM Co, <20pM La). Dissolved Fe, Mn, Ni and Cd were below our detection limits of 13 nM, 1. 8 nM, 4.7 nM and 15pM (respectively) in surface waters. There was a 6-m vertical separation in the onset of Mn and Fe reduction, with dissolved Mn appearing higher in the water column than Fe. Based on thermodynamic calculations, dissolved Mn appears to be controlled by equilibrium with hausmannite (Mn3O4). Co tracks the Mn profile closely, suggesting Co(III) is bound in the lattice of Mn oxides, whereas the Ce profile is similar, yet the Ce anomaly suggests oxidative scavenging of Ce. Release of Cu, Ni, Cd and trivalent REE appears to be controlled by pH-induced desorption from Fe and Mn oxides, although Cu (and perhaps Ni) may be scavenged by organic matter in surface waters.     

Geochemical fractionation and ecological risks assessment of benthic sediment-bound heavy metals from coastal ecosystems off the Equatorial Atlantic Ocean

This study determines the pollution, fractionation, and ecological risks of sediment-bound heavy metals from coastal ecosystems off the Equatorial Atlantic Ocean. Contamination Factor(CF), pollution load index(PLI), and geoaccumulation index(Igeo) were used to assess the extent of the heavy metal pollution, while the potential ecological risk was evaluated using the risks assessment code(RAC) and Hkanson potential ecological risk. The analysis revealed concentrations(mg/g, dw) of the cadmium(Cd),chromium(Cr), copper(Cu), nickel(Ni), and lead(Pb) in sediments for wet and dry seasons vary from 4.40-5.08, 14.80-21.09. 35.03-44.8, 2.14-2.28, and 172.24-196.39, respectively. The results also showed that the metal fractionation percentages in the residual, oxidizable, and reducible fractions are the most significant, while the exchangeable and carbonate bound trace metals are relatively low. The RAC values indicate no risk for Cd and Ni and low risk for other metals at all the studied sites during both seasons.Potential ecological risk analysis of the heavy metal concentrations indicates that Cd had high individual potential ecological risk, while the other metals have low risk at all investigated sites. The multi-elemental potential ecological risk indices(R_1) indicate high ecological risk in all the ecosystems.     

Evolving metasomatic agent in the Northern Andean subduction zone, deduced from magma composition of the long-lived Pichincha volcanic complex (Ecuador)

Geochemical studies of long-lived volcanic complexes are crucial for the understanding of the nature and composition of the subduction component of arc magmatism. The Pichincha Volcanic Complex (Northern Andean Volcanic Zone) consists of: (1) an old, highly eroded edifice, the Rucu Pichincha, whose lavas are mostly andesites, erupted from 1,100 to 150 ka; and (2) a younger, essentially dacitic, Guagua Pichincha composite edifice, with three main construction phases (Basal Guagua Pichincha, Toaza, and Cristal) which developed over the last 60 ka. This structural evolution was accompanied by a progressive increase of most incompatible trace element abundances and ratios, as well as by a sharp decrease of fluid-mobile to fluid-immobile element ratios. Geochemical data indicate that fractional crystallization of an amphibole-rich cumulate may account for the evolution from the Guagua Pichincha andesites to dacites. However, in order to explain the transition between the Rucu Pichincha andesites and Guagua Pichincha dacites, the mineralogical and geochemical data indicate the predominance of magma mixing processes between a mafic, trace-element depleted, mantle-derived end-member, and a siliceous, trace-element enriched, adakitic end-member. The systematic variation of trace element abundances and ratios in primitive samples leads us to propose that the Rucu Pichincha magmas came from a hydrous-fluid metasomatized mantle wedge, whereas Guagua Pichincha magmas are related to partial melting of a siliceous-melt metasomatized mantle. This temporal evolution implies a change from dehydration to partial melting of the slab, which may be associated with an increase in the geothermal gradient along the slab due to the presence of the subducted Carnegie Ridge at the subduction system. This work emphasizes the importance of studying arc-magma systems over long periods of time (of at least 1 million of years), in order to evaluate the potential variations of the slab contribution into the mantle source of the arc magmatism.     

Ion winds in Saturn's southern auroral/polar region

We present profiles of the line-of-sight (l.o.s.) ionospheric wind velocities in the southern auroral/polar region of Saturn. Our velocities are derived from the measurement of Doppler shifting of the H₃⁺ν₂Q(1,0⁻) line at 3.953 microns. The data for this study were obtained using the facility high-resolution spectrometer CSHELL on the NASA Infrared Telescope Facility (IRTF) on Mauna Kea, Hawaii, during the night of February 6, 2003 (UT). The l.o.s. velocity profiles finally derived are consistent with an extended region of the upper atmosphere sub-corotating with the planet: the ion velocities in the inertial reference are only 1/3 of those expected for full planetary corotation. We discuss the results in the light of recent proposals for the kronian magnetosphere, and suggest that, in this region, Saturn's ion winds may be under solar wind control.     

Baja California 边缘PC14 岩芯海水表层温度及生产力变化的百年尺度记录

加利福尼亚流是北太平洋环流的重要组成部分,它的变化对全球气候及碳循环有重要影响.对位于东北太平洋低纬区BajaCalifornia外海的PC14柱状样进行了有机地球化学分析,重建了过去14ka来这一地区百年尺度的海水表面温度及生产力变化,发现其存在明显的B/A(Bling-Aller)和YD(Younger Drays)事件,但B/A和YD事件温度变化幅度小于中纬度地区.与中纬度加利福尼亚流系早中全新世温度降低不同,PC14全新世温度无明显变化趋势.这些结果表明了东太平洋低纬地区对高纬地区的气候响应以及沿岸上升流和ENSO现象对加利福尼亚流系中纬和低纬地区的影响不同.从冰消期到全新世,PC14生产力呈现阶段上升趋势,指示了由E1 Nino气候向La Nifia气候的转化以及沿岸上升流加强的总体趋势.在全新世中后期(6.5-3.8ka)生产力的降低,则可能是受ENSO加强的影响.在B/A暖期,PC14生产力增加不多,但氧最小层强度增加,这表明生产力变化不是东太平洋边缘海的氧最小层强化的控制因素.     

Excess air during aquifer storage and recovery in an arid basin (Las Vegas Valley, USA)

The Las Vegas Valley Water District in Nevada, USA, has operated an artificial recharge (AR) program since 1989. In summer 2001, observations of gas exsolving from tap water prompted a study that revealed total dissolved gas (TDG) pressures approaching 2?atm with a gas composition that it is predominantly air. Measurements of TDG pressure at well heads and in the distribution system indicated two potential mechanisms for elevated TDG pressures: (1) air entrainment during AR operations, and (2) temperature changes between the winter recharge season and the summer withdrawal season. Air entrainment during pumping was investigated by intentionally allowing the forebay (upstream reservoir) of a large pumping station to drawdown to the point of vortex formation. This resulted in up to a 0.7?atm increase in TDG pressure. In general, the solubility of gases in water decreases as the temperature increases. In the Las Vegas Valley, water that acquired a modest amount of dissolved gas during winter artificial recharge operations experienced an increase in dissolved gas pressure (0.04?atm/°C) as the water warmed in the subsurface. A combination of air entrainment during AR operations and its amplification by temperature increase after recharge can account for most of the observed amounts of excess gas at this site.