Quasi-3-yr Cycle of Rainy Season Precipitation in Tibet Related to Different Types of ENSO during 1981–2015

The rainy season precipitation in Tibet (RSPT) is a direct cause for local floods/droughts. It also indirectly affects the thermal conditions of the Tibetan Plateau, which can result in anomalous patterns of atmospheric circulation over East Asia. The interannual variability of the RSPT is often linked with the El Niño–Southern Oscillation (ENSO), but the relevant mechanisms are far from being understood, particularly for different types of ENSO events. We investigated the interannual variation of the RSPT in association with different types of ENSO. A quasi-3-yr period of the RSPT (less–more–more precipitation) was significant at the 95% confidence level. A joint multi-taper method with singular value decomposition analysis of the coupled field between the RSPT and the sea surface temperature (SST) revealed that the developing eastern Pacific type El Niño was accompanied by a decrease in the RSPT. The shift from the central Pacific type El Niño to the eastern Pacific La Niña was accompanied by an increase in the RSPT. Weakening of the central Pacific La Niña was accompanied by an increase in the RSPT. Analysis of the mechanism of this coupling, using the same analysis method but other climatic factors, indicated that the gradually strengthening eastern Pacific El Niño can inhibit the Walker circulation, weakening the South Asian summer monsoon, and resulting in transport of less water vapor from the Bay of Bengal to Tibet. The change from the central Pacific El Niño to the eastern Pacific La Niña led to continued strengthening of the Walker circulation with westward movement of the ascending area. This enhanced the South Asian summer monsoon over the Arabian Sea and transported more water vapor to Tibet. The decreasing central Pacific La Niña accompanied by persistent cooling of SSTs in the equatorial Pacific led to a strong eastern North Pacific summer monsoon, causing an anomaly in the easterly transport of water vapor from the Sea of Japan to Tibet and increased RSPT.     

长白山火山喷发物的堆积类型及火山活动机理

本文对长白山火山地质发展过程中的两大喷发期和七个喷发阶段作了系统阐述,详细划分、描述了喷发物堆积类型及特征,论述了火山活动机理及演化历程。首次指出长白山火山基浪堆积,对新发现的侵入相和次火山岩相岩百与喷出相岩石做了对比,指出同源于一个碱性岩浆房。     

超高压变质岩矿物中的显微构造缺陷:来自TEM和FTIR研究的证据

超高压变质矿物的某些显微构造缺陷可能指示了岩石短暂和快速抬升过程。文中报道了中国大别山双河地区超高压硬玉石英岩矿物显微构造缺陷的透射电镜(TEM)和Fourier变换红外光谱(FTIR)的研究结果。用TEM研究方法,在硬玉石英岩中硬玉包裹体内发现了亚微米级天然蒙钠长石(MA,C2/m)、高钠长石(HA,C)和低钠长石(LA,C)三种多形变体。表明岩石在折返过程经历过高温变质作用(>930℃),以及退变质过程的快速冷却;在石英包裹体内发现了纳米级柯石英和石盐子矿物,提供了柯石英转变为石英以及峰期变质条件下高盐流体存在的证据。"名义上无水矿物"(NAMs)的结构水(OH/H2O)是以缺陷形式赋存于矿物结构中。FTIR分析结果显示硬玉、石榴石、金红石和石英中结构水的平均含量分别为1000×10-6、(900~1600)×10-6、>2000×10-6和<4×10-6,硬玉石英岩全岩含水量为(490~600)×10-6,表明在高压-超高压变质作用过程中,地壳或原岩中的水可以通过这些NAMs携带到地球深部。该类显微构造缺陷可能是大陆碰撞造山带在高应变速率下的局部弱化和深部断层作用的结果。     

Glauconites from the Late Palaeocene — Early Eocene Naredi Formation,western Kutch and their genetic implications

Glauconitic minerals are considered as one of the valuable input parameters in sequence stratigraphic analysis of a basin. In the present study glauconitic minerals are reported from subtidal green shale facies in the lower part of the Late Paleocene-Early Eocene Naredi Formation of western Kutch. On the basis of the foraminiferal assemblage the glauconite bearing beds are interpreted to have formed in a mid shelf depositional settings of an unstable marine conditions. XRD studies confirm the glauconite mineralogy of the green pellets and provide an estimation of glauconite maturity. Textural attributes of the glauconites confirm their derivation by different degrees of alteration of precursor feldspar grains. Because of the authigenic origin and autochthonous nature, these glauconites hold promise for understanding sequence stratigraphy of the Palaeogene succession of the western Kutch.     

内蒙古阿巴嘎旗乌和尔楚鲁图钼矿区成矿斑岩的岩石地球化学特征与年代学

乌和尔楚鲁图钼矿床位于国内重要的二连东乌旗钼矿成矿带中,为近几年新发现的斑岩型钼矿床.本次就该矿床成矿岩体的地球化学及其U-Pb年代学开展相关研究.结果表明: 矿区中的成矿岩体属过铝质、高钾钙碱性系列;富集大离子亲石元素(LILE)、亏损高场强元素(HFSE),具有与南岭型花岗岩相似的地球化学特征.锆石LA-ICP-MS U-Pb定年显示,与乌和尔楚鲁图钼矿床成矿有关的花岗斑岩形成于中侏罗世((160 ± 1)Ma).因此,可推测乌和尔楚鲁图钼矿床斑岩型钼矿的成矿时代为燕山早期.综合研究认为乌和尔楚鲁图斑岩型钼矿床形成于后碰撞的构造环境.     

Textural evidences for dissolution of silica-rich rocks of the Ypresian phosphatic series,Gafsa-Metlaoui basin,southwestern Tunisia: implication of biogenic silica supply on genesis of fibrous clays

The present work aimed to determine the mineralogical composition of Ypresian series and to clarify the influence of the dissolution of siliceous frustules on the genesis of fibrous clay minerals. The specimens sampled from CPG trench are mainly constituted of silica-rich rocks at Mides area located at the western part of Gafsa-Metlaoui basin. The samples were investigated using X-ray diffraction (XRD) and scanning electron microscopy (SEM) in order to determine texture of constituents. The data obtained indicate that the bulk rock samples are mainly made up of opal CT and clay minerals. The latter consists of palygorskite-sepiolite minerals associated with smectite and few amount of illite. The trend of mineralogical composition indicates that fibrous clay minerals are more concentrated at the upper part. SEM observations indicated that palygorskite mineral appears as thread-like facies, which surround foliated texture of smectite in the lower part of the Mides section, although with the low Mg activity confirmed by the absence of dolomite. But, at the upper part of the Mides section, SEM observations revealed the occurrence of siliceous frustules, which have numerous dissolved areas and replacement of carbonate tests by silica. The dissolution saturated the depositional environment with silica which is required for the formation of palygorskite and sepiolite minerals, in addition to high Mg activity confirmed by the presence of dolomite in the bulk rock, which is required basically for the formation of sepiolite. Although the genesis mode of palygorskite and sepiolite is similar with very little difference, the genesis of sepiolite needs a high alkalinity than the formation of palygorskite.     

Structure and oxidation state of hematite surfaces reacted with aqueous Fe(II) at acidic and neutral pH

Structural changes and surface oxidation state were examined following the reaction of hematite (0 0 1), (0 1 2), and (1 1 0) with aqueous Fe(II). X-ray reflectivity measurements indicated that Fe(II) induces changes in the structure of all three surfaces under both acidic (pH 3) and neutral (pH 7) conditions. The structural changes were generally independent of pH although the extent of surface transformation varied slightly between acidic and neutral conditions; no systematic trends with pH were observed. Induced changes on the (1 1 0) and (0 1 2) surfaces include the addition or removal of partial surface layers consistent with either growth or dissolution. In contrast, a <1 nm thick, discontinuous film formed on the (0 0 1) surface that appears to be epitaxial yet is not a perfect extension of the underlying hematite lattice, being either structurally defective, compositionally distinct, or nanoscale in size and highly relaxed. Resonant anomalous X-ray reflectivity measurements determined that the surface concentration of Fe(II) present after reaction at pH 7 was below the detection limit of approximately 0.5-1 μmol/m² on all surfaces. These observations are consistent with Fe(II) oxidative adsorption, whereby adsorbed Fe(II) is oxidized by structural Fe(III) in the hematite lattice, with the extent of this reaction controlled by surface structure at the atomic scale. The observed surface transformations at pH 3 show that Fe(II) oxidatively adsorbs on hematite surfaces at pH values where little net adsorption occurs, based on historical macroscopic Fe(II) adsorption behavior on fine-grained hematite powders. This suggests that Fe(II) plays a catalytic role, in which an electron from an adsorbed Fe(II) migrates to and reduces a lattice Fe(III) cation elsewhere, which subsequently desorbs in a scenario with zero net reduction and zero net adsorption. Given the general pH-independence and substantial mass transfer involved, this electron and atom exchange process appears to be a significant subsystem within macroscopic pH-dependent Fe(II) adsorption.     

Sorption behaviour of pentachlorophenol in sub-Saharan tropical soils: soil types sorption dynamics

In order to predict exposure risks as well as appropriate remediation strategies for pesticides in soils, knowledge of pesticides sorption processes onto various representative soils is vital. Hence, laboratory batch experiments were carried out to study sorption of a pesticide, pentachlorophenol (PCP), on five soils obtained from different sub-Saharan agro-ecological zones (AEZs) in order to understand sorption equilibrium, kinetics, and thermodynamics. Experimental data showed that sorption equilibrium was attained within 24 h. The fitting of kinetic results and equilibrium data to different models suggested partly surface adsorption and partly partitioning of PCP within voids of the various soil components. Sorption was mainly attributed to sharing or exchange of valence electrons between negatively charged PCP molecules and positively charged soil sorption sites. The sorption process was spontaneous and accompanied by decreased entropy, but was pH and temperature dependent, reducing with increase in pH and temperature. The various soils’ PCP sorption capacities were directly proportional to their cation exchange capacities. The low PCP sorption observed in these soils suggested high risk of PCP being present in soil water solution, especially at higher temperatures, which can lead to contamination of the aquifer. This risk may be higher for soils obtained from AEZs with warmer natural temperatures.     

Precambrian crystalline basement in southern Mongolia as revealed by SHRIMP zircon dating

Single zircon ages determined by ion microprobe (SHRIMP II) for granitoid gneisses from the southern slope of the Baga Bogd massif (Gobi-Altai, southern Mongolia) reveal several episodes of zircon growth, ranging from late Palaeoproterozoic to late Cambrian. The oldest events are documented by a zircon crystallization age for a gneiss protolith at 1519 ± 11 Ma and by a xenocrystic zircon from a dark grey augen-gneiss yielding an age of c. 1701 Ma. Discrete igneous events are recorded in granite-gneisses with protolith emplacement ages of 983 ± 6, 956 ± 3 and 954 ± 8 Ma. These ages provide the first record of early Neoproterozoic magmatic activity in this region. A much younger and discrete magmatic event is recorded by several dioritic to granitic orthogneisses which are tectonically interlayered with the older gneisses and have protolith emplacement ages between 502 and 498 Ma. These late Cambrian granitoids of calc-alkaline affinity are likely to have been emplaced along an active continental margin and suggest that the Baga Bogd Precambrian crustal fragment was either docked against the southward (present-day coordinates) growing margin of the CAOB or was a large enough crustal entity to develop an arc along its margin. We speculate that the Precambrian gneisses of this massif may be part of a crustal fragment rifted off the Tarim Craton.     

Enhancement of removal efficiency of ammonia nitrogen in sequencing batch reactor using natural zeolite

Two sets of lab-scale sequencing batch reactors (SBR), i.e., control SBR and SBR using zeolite as carrier (zeo-SBR), were applied to assess nitrogen removal efficiency. The test results revealed that zeolite powder added in SBR could improve its performance. Due to the combination of zeolite adsorption for NH₄ ⁺–N and enhanced simultaneous nitrification and de-nitrification (SND), a higher removal ratio of ammonia nitrogen in wastewater was observed in the test reactor, and the introduction of zeolite powder was helpful to inhabit sludge bulging comparing with the control SBR, in other words, activated sludge immobilized by zeolite powder could remove NH₄ ⁺–N, COD, and PO₄ significantly in a shorter cycle time. Applied two hydraulic retention times (HRTs) showed that the nitrogen and phosphorus removal could be improved while adapting to load variations.