Variations in Stable Carbon Isotopic Composition of n-Alkanes from Ordovician- and Triassic-Derived Oils in Lunnan Oilfield, Tarim Basin, NW China: Global Paleoenvironmental Constraints

1IntroductionInthelastdecade,theGC C IRMStechniquehasbeenwidelyappliedinthestudyoffossilfu els (Bjoryetal.,1 990 ,1 991 ,1 992 ,1 994a ,1 994b ;Schoelletal.,1 994) ,biomarkers (Schoelletal.,1 992 )andpaleoenvironment(Pancostetal.,1 999) ,aswellasofpaleoceanography (Kenni cuttetal.,1 990 ) ,biogeochemistry (e .g .Hayesetal.,1 990 )andenvironmentalsciences (O’Malleyetal.,1 994) .Stablecarbonisotopicanalysesweremadeofacoupleofcompound specifictypesincludingn alkanes,isoprenoids,lighthydr…     

REE and Trace Element Geochemistry of Yinachang Fe-Cu-REE Deposit, Yunnan Province, China

1IntroductionThebehaviorsoftherare earthelements (REE)duringmagmatism ,metamorphismandmeta somationareofgreatgeologicalinterestbecauseoftheirapplicationsingeochronologyandgeochemi caltracing (e .g .reviewsbyFaure ,1 986;LipinandMckay ,1 989) .Becauseoftheirsimilargeo chemicalbehaviorsandlowsolubilitiesinwater,theREEshaveprovedthemselvestobeapowerfultoolforthecharacterizationofprovenanceswhenappliedtosedimentaryrocks (McDanieletal.,1 994) .Althoughtheirbehaviorsunderhydrothermalconditionsar…     

Formation Waters and Their Relations to Natural Gas Reservoirs in Central Ordos Basin

1IntroductionFormationwaterisanimportantmediumforhydrocarbongenerationandmigration .Thelong termcontactofformationwaterswithoilandgasmustleavesomeorganiccomponentsintheforma tionwaters.Ofcourse,thechemicalcompositionofformationwater (i.e.,oilfieldwater)iscloselyrelatedtotheformationofoilandgasreservoirs (Collins,1 975) .Since 1 970smanyscholarsbothathomeandabroadhavecenteredonthestudyofthecharacteristicsofformationwatersthemselves(Collins,1 975;LiuChongxi,1 988;HuangFutangetal.,1 993 ;GaoX…     

Sm-Nd AND Rb-Sr AGES AND GEOCHEMISTRYOF VOLCANICS FROM THE DINGYUANFORMATION IN DABIE MOUNTAINS,CENTRAL CHINA: EVIDENCE TO THE PALEOZONIC MAGMATIC ARC

1.IntroductionTheDabieMountainsisacollisionzonebetWeentheNorthChinablock(NCB)andSouthChinablock(SCB).Varioustypesofultrahigh-pressuremetamorphic(UHPM)rocksincludingcoesiteanddiamond-heiringeclogiteareexposedintheDabieMountains(Okayetal.1989;Wangetal.1989;Xuetal.1992a).Itis,ingeneral,acceptedthattheDabieMountainscanbesubdividedintofourtectonicsubzonesfromtheNorthtotheSouth:(1)Beihuaiyang,greenschist--amphibolitefacteszone.(2)NorthDabiecomplex(terrane).(3)SouthDabieultrahighpressurem…     

透辉石结构中M_1位Fe~(2 )离子晶场谱带的理论解释

根据B.E.沃伦(Warren,1929)和W.L.布雷格(Bragg,1929)的测定,透辉石中的Fe~(2 )离子有两种占位情况:M_1占位的Fe~(2 )有六个配位氧原子,与正八面体配位相近似;M_2占位的Fe~(2 )也有六个配位氧原子,但较正八面体配位有很大的畸变。 W.B.怀特(White,1966)和K.L.基斯特(Keester,1966)用非偏振吸收光谱方法测定了含5％CaFeSi_2O_6的透辉石样品的三条吸收带为13600cm~(-1)、9730cm~(-1)、4420cm~(-1)。肯定了强吸收带9730cm~(-1)是由M_1位的Fe~(2 )离子的d电子在晶场分裂能级间自旋允许跃迁引起的,弱吸收带13600cm~(-1)象是属于Fe~(2 )离子的,宽而弱的带4420cm~(-1)象是由少量的四配位Fe~(2 )离子引起的。     

Thermal Ionization Mass Spectrometry （TIMS）－U－Series Ages of Corals from the South China Sea and Holocene High Sea Level

1IntroductionTostudyglobalchangesinthepast (PAGES) ,i.e.,paleo climaticandpaleoenvironmentalchanges,itisnecessarytoestablishahigh resolutionandhigh precisiontimescale .Lateinthe1 980s,Edwardsetal.( 1 987,1 987)developedthethermalionizationmassspectrometry U seriesdatingmethod (TIMS)andtheyusedthismethodtoconducttheprecisedatingofthecharacteristicclimateeventssincethelastinterglacialperiod .Theirscientificpracticearousedgreatinterestofsci entificworkersengagedinQuaternaryenvironment (Peng…     

南黄海表层沉积物中氮的分布特征及其在生物地球化学循环中的功能

本文报道了南黄海表层沉积物中不同形态氮的区域分布特征及其在生物地球化学循环中的作用。结果显示 ,在粒径 <31 μm的粒度组分含量 >6 5 %( )、35 %～ 6 5 %( )和 <35 %( )的三个区域中 ,沉积物中不同形态氮的含量比值分别为 :1 .6 5 :1 .2 6 :1 (IEF- N) ,1 .2 3:1 .1 0 :1 (WAEF- N) ,1 .4 1 :1 .0 4 :1 (SAEF- N) ,2 .0 8:1 .4 5 :1 (SOEF- N) ,TN(1 .70 :1 .2 6 :1 ) ,即在细粒度组分 (<31 μm)含量较高的区域 ,不同形态氮的含量也相对较高 ;在三个分区内 ,不同形态氮的埋藏通量非常相近 ,而埋藏效率自 至 区逐渐递增 ,在细粒度组分 (<31 μm)含量最低的 区内 ,埋藏效率最高 ,TN的埋藏效率可达 30 .2 1 %,即南黄海表层沉积物中 70 %以上的氮在适当的条件下可释放进入水体参与其生物地球化学循环 ,能提供海洋新生产力所需氮的 6 .5 4 %,对海洋生产力具有一定的补充和调控作用。     

The dynamics of organic matter in soil size and density fractions traced by stable carbon isotopes

1IntroductionSoilorganicmatter (SOM)isakeysourceofnutrientsforplantgrowth ,itisessentialforthemaintenanceofsoilstructureanditcontributestotheabilityofsoiltoretainnutrientsandwater.AnimprovedunderstandingofSOMdynamicsiscentraltothedevelopmentofmoreenvironmentallysoundandsustainablepracticesofagriculturalmanagement (Collinsetal.,2 0 0 0 ) .Avarietyofcon ceptualmethodshavebeenusedtodescribetheprocessesofSOMaccumulationandturnover (Jen kinsonandRayner,1 977;Duxburyetal.1 989;Partonetal.,1 99…     

华东某地矽卡岩型铜矿成矿规律探讨

一、区域地质简述(一)地层区内出露沉积地层以古生界为主.自寒武系到侏罗系沉积地层厚约3200米,其中:1.碳酸盐岩层厚约2000米,由观音台组?、仑山组(O_1~1)、红花园组(O_1~2)、大湾组(O_1~3)、汤山组(O_2)、金陵组(C_1~1)、和州组(C_1~3)、老虎洞组(C_1~4)、黄龙组(C_2)、船山组(C_3)、栖霞组(P_1~1)、青龙群(T_(1 2))组成;2.碎屑岩层厚约1200米,由五峰组     

洱海沉积物间隙水中溶解有机质的地球化学特性

对洱海沉积物间隙水中溶解有机质(DOM)含量、紫外可见吸收、荧光以及分子量等的垂直分布特征进行了研究。结果表明,DOC含量在沉积物水界面明显富集,随后急剧下降,6cm处达到最小值,随后呈上升趋势。DOC与吸光度值、荧光发射光谱强度之间具有一定的线性相关关系。DOM的E3/E4值范围在1～6之间,绝大多数在1～35之间。表征DOM中腐殖质来源的指标荧光指数值处于148～159之间,说明DOM以陆源输入为主。此外,洱海沉积物间隙水DOM分子量分布呈多峰分布模式,重均分子量(M_w)值在1462～1953Da之间,数均分子量(M_n)值在547～900Da之间,多分散性系数ρ值在202～305之间。随着沉积深度增大,M_w和M_n有略微的增大趋势,但变化不大。沉积物的氧化还原条件、微生物活动以及铁、锰氧化物等在沉积剖面的差异是控制间隙水中DOM各种地球化学特性的主要因素。     

Effects of water chemistry and concentrations of dissolved organic matter on its fluorescence characteristics and molecular conformation

Previous studies showed that water chemistry and concentrations of dissolved organic matter (DOM) could affect its molecular conformation and binding characteristics with hydrophobic organic contaminants (HOCs). However, the conformational change of DOM resultant from water chemistry and concentrations of DOM was not extensively investigated; therefore, the contradictory reports regarding the binding property with HOCs were available in literature. In this study, the effects of ionic strength, pH and DOM concentrations on the fluorescence properties of two humic acids (HA), namely Fluka HA and Amherst HA, were investigated by three-dimensional excitation-emission matrix fluorescence spectroscopy (3DEEM) and steady-state fluorescence polarization (FP) techniques. The results not only corroborated previous observations obtained by other investigators, but revealed some new information about the fluorescence properties and molecular conformation of the humic acids under different water chemistry and DOM concentration conditions, which could shed light on its binding mechanisms and binding properties with HOCs.     

卤水中溶解性有机质的光谱学性质和光降解行为研究

卤水中溶解性有机质(dissolved organic matter,DOM)会对盐田日晒工艺和产品质量产生不利影响,如盐田卤水的蒸发速率减缓、蒸发度减小以及提取的矿物产品带有刺鼻的气味、浓重的颜色等。因此,对具有资源开发利用价值的卤水体系中DOM结构和性质的研究可以为后续DOM的有效去除或在DOM共存体系中调控无机盐结晶工艺路线提供有效的指导意见。本文以自然界中广泛存在的两种不同类型的卤水体系,即盐湖卤水DOM(SLDOM)和油田卤水DOM(OFDOM)为研究对象,采用溶解性有机碳(dissolved organic carbon,DOC)分析、光谱学分析和平行因子分析等手段对DOM的含量、分子量分布特征、光谱学结构和光降解行为开展了研究。DOC和荧光分析表明SLDOM和OFDOM的DOC含量和生物指数(BIX)值相似;与OFDOM相比,SLDOM的腐质化指数(HIX)值和高分子量组分(HMW)比例偏高;特别吸收光谱(SUVA₂₅₄)和糖类化合物含量检测结果表明,SLDOM和OFDOM的HMW组分中含有的芳香类和糖类化合物所占比例比低分子量组分(LMW)高;三维荧光谱图分析(EEM)结果表明,SLDOM主要以腐殖质类物质为主,而OFDOM以蛋白质类组分为主。此外,DOM的荧光组分在不同分子量中的分布也存在明显差异:对于SLDOM,富里酸主要分布在HMW DOM中,而腐殖酸主要在LMW DOM中;对于OFDOM,芳香胺类蛋白组分主要分布在HMW DOM中,色氨酸和酪氨酸类蛋白组分主要分布在LMM DOM中。在光降解实验中,SLDOM和OFDOM的DOC含量随光照时间增加而逐渐减少,分别下降了29.32%和15.11%。进一步的分析表明,光照过程中两种卤水中糖类化合物均减少,小分子量的DOM优先分解。此外,在光照过程中SLDOM芳香类化合物增加,腐质化程度基本不变;OFDOM芳香类化合物减少,腐质化程度增加。EEM平行因子分析(PARAFAC)结果表明,SLDOM荧光组分在光降解过程中荧光强度增加,而OFDOM荧光强度减少。     

DOM不同分子质量组分对石英砂吸附卡马西平的影响研究

为探究溶解性有机质(DOM)不同相对分子质量组分对药物和个人护理品(PPCPs)类污染物吸附过程的影响,以卡马西平(CBZ)为目标污染物,以石英砂代表无机矿物,用商用腐殖酸(HA)制备DOM并进行超滤分级,然后开展吸附实验,并采用荧光光谱和红外光谱表征等手段,研究了DOM不同分子质量组分对石英砂吸附CBZ的影响及机制。结果表明,以3 000和10 000的超滤膜进行分级后的不同相对分子质量HA结构有明显差别,大分子质量HA中苯环等疏水性结构以及羟基的含量较多,芳香构造化程度高,多为分子量较高、稳定性较好的疏水性有机物,但中、小分子质量HA结构差异不大,含有更多羰基、羧基等含氧官能团,主要是一些分子质量较小的亲水物质; DOM不同分子质量组分对CBZ在石英砂上的吸附有明显影响,其中大分子质量组分促进吸附,而中、小分子质量组分抑制吸附,原因在于大分子质量组分可疏水结合于矿物表面,增加介质表面的活性吸附位点,同时其芳香性或脂肪性结构可与CBZ的疏水基团发生疏水作用共吸附或累积吸附于介质表面,从而促进CBZ的吸附;而中、小分子质量DOM的极性官能团可与CBZ酰胺部分通过极性作用结合,对CBZ分子有增溶作用,从而抑制吸附。     

The behaviour of dissolved organic material,iron and manganese in estuarine mixing

Fractionation by ultra-filtration of the dissolved organic material (DOM) in the River Beaulieu, with typical concentrations of dissolved organic carbon (DOC) of 7–8 mg C/l, showed it to be mainly in the nominal molecular weight range of 10³–10⁵, with 16–23% of the total DOC in the fraction > 10⁵. The molecular weight distribution of DOM in the more alkaline River Test (average DOC, 2 mg C/l) was similar. In the River Beaulieu water, containing 136–314 βg Fe/l in ‘dissolved’ forms, 90% or more of this Fe was in the nominal molecular weight fraction > 10⁵. Experiments showed that DOM of nominal molecular weight <10⁵ could stabilize Fe(III) in ‘dissolved’ forms. The concentrations of ‘dissolved’ Fe in the river water probably reflect the presence of colloidal Fe stabilized by organic material and this process may influence the apparent molecular weight of the DOM. Dissolved. Mn (100–136 βg/l) in the River Beaulieu was mainly in true solution, probably as Mn(II), with some 30% in forms of molecular weight greater than ca 10⁴.During mi xing in the Beaulieu Estuary, DOC and dissolved Mn behave essentially conservatively. This contrasts with the removal of a large fraction of the dissolved Fe (Holliday and LISS, 1976, Est. Coastal Mar. Sci. 4, 349–353). Concentrations of lattice-held Fe and Mn in suspended particulate material were essentially uniform in the estuary, at 3.2 and 0.012%, respectively, whereas the non-lattice held fractions decreased markedly with increase in salinity. For Mn the decrease was linear and could be most simply accounted for by the physical mixing of riverborne and marine participates, although the possibility that some desorption occurs is not excluded. The non-linear decrease in the concentration of non-lattice held Fe in particulates reflected the more complex situation in which physical mixing is accompanied by removal of material from the ‘dissolved’ fraction.     

Airborne Laser-Induced Fluorescence (LIF) Light Detection and Ranging (LiDAR) for the Quantification of Dissolved Organic Matter Concentration in Natural Waters

Analysis of dissolved organic matter (DOM) concentration and composition is essential to quantifying biological and chemical oxygen demand and atmosphere?Cocean heat flux exchange in natural waters. However, manual water sampling is costly and time consuming over large areas. The purpose of this research was to analyze the applicability of airborne laser-induced fluorescence light detection and ranging (LiDAR) for the detection of DOM in estuarine ecosystems impacted by agriculture. A fluorescence LiDAR system (Airborne Marine) (FLS-AM) was used to assess the DOM concentration of the Annapolis River and Basin, Nova Scotia, Canada, as well as three rivers and their estuaries in Prince Edward Island, Canada. Two FLS-AM flight missions were conducted in the summers of 2008 and 2009 and the resulting datasets were compared with spectral fluorescence signature (SFS DOM) and dissolved organic carbon (DOC) analysis of in situ water samples. Significant positive correlations were found at five of seven sites between the FLS-AM DOM and SFS DOM relationship which indicates that the FLS-AM sensor is a good surrogate for traditional sample collection of DOM data in estuaries in this region. Positive correlations were also found at all sites between FLS-AM DOM values and DOC. FLS-AM DOM patterns show that DOM values are significantly higher in rivers and estuaries that drain watersheds which are heavily impacted by agricultural practices. The results of this study show that the FLS-AM can be used efficiently as a general indicator for how estuaries are affected by runoff from agricultural watersheds in real time and thus reduce the requirement for traditional water sample collection and laboratory analysis methods.     

Effects of photoirradiation on the adsorption of dissolved organic matter to goethite

The effects of photoirradiation of dissolved organic matter (DOM) on its subsequent adsorption to the Fe(III)oxyhydroxide mineral goethite were investigated at 22°C in 0.10 mol L⁻¹ NaClO₄ solutions at pH 3.5 and 5.5, Photoirradiation of DOM decreased the abundance of high molecular-weight components and formed new lower molecular-weight components, including low molecular weight carboxylic acids (i.e., formic, malonic, and acetic acids). Adsorption of non-irradiated DOM decreased from pH 3.5 to 5.5 and was dominated by the intermediate molecular weight (1251-3750 Da) fraction, although the 451-1250 and 3751-11350 Da fractions also contributed to adsorption at pH 3.5. Irradiation resulted in a substantial decrease in DOM adsorption affinity at pH 3.5, primarily due to loss of components in the 1251-3750 and 3751-11350 Da fractions. Irradiation resulted in only a small decrease in DOM adsorption affinity at pH 5.5; the loss of components in the 3751-11350 Da fraction upon irradiation had little effect on adsorption because they played little or no role in the non-irradiated sample at this pH. Irradiation of DOM also affected its interactions with Fe in solution and the solution iron(II)/iron(III) speciation. The combined effects of irradiation followed by adsorption produced DOM that was lower in molecular weight and had a decreased UV-Vis absorptivity than either process, alone. Together, these two processes are likely to have important environmental consequences in terms of UV penetration of surface waters, contaminant mobility, and DOM bioavailability.     

不同地质年代煤矸石中有机质的溶出特征对比

分别以神东矿区补连塔矿侏罗纪煤矸石和保德矿二叠纪煤矸石为研究对象,通过浸泡实验,结合三维荧光光谱测试技术及平行因子分析法,对比研究2种煤矸石中有机质的溶出特征,这对于开展煤矿区地下水库水处理机理研究具有重要意义。研究结果表明:由于煤矸石自身矿物组成不同,补连塔矿煤矸石浸泡液中总离子质量浓度高于保德矿,且2种煤矸石浸泡液均呈弱碱性;其中补连塔矿煤矸石溶解性有机质（DOM）中含有较多的共轭双键或苯环类简单芳香族化合物,以富里酸和分子量较大的陆源类腐殖质为主,且含量普遍高于保德矿,而保德矿煤矸石中富里酸和酪氨酸类有机质较多。根据DOM样品荧光指数（FI）、生物源指数（BIX）、腐殖化指数（HIX）的计算结果,2种煤矸石中DOM主要为内源有机质,并具有较强的自生源特征,且煤矸石形成地质年代越早,煤矸石DOM样品的"微生物源"特征越明显。      

洱海沉积物孔隙水中溶解有机质的三维荧光光谱特征

文章应用三维荧光光谱技术对洱海沉积物孔隙水中的溶解有机质进行了研究。结果表明,所有样品均含有4个明显的荧光峰,其中A和C为类腐殖酸荧光,B和D为类蛋白荧光。荧光强度在沉积物-水界面特别强,在1cm处急剧下降,之后随着沉积深度呈上升趋势。孔隙水溶解有机质均具有强的类蛋白荧光,揭示了溶解有机质中含有大量色氨酸、酪氨酸等芳环结构的类蛋白物质,并且在早期成岩过程中随着沉积深度呈积累趋势;类蛋白荧光与类腐殖酸荧光之间具有一定的相关关系,r(A,C)值在0.94-1.79之间,随着沉积深度逐渐下降,r(D,B)值在0.9-1.75之间,与r(A,C)值极为接近,且随着沉积深度有着类似的变化趋势,说明在洱海沉积物孔隙水中,r(D,B)与r(A,C)之间具有一定的相关性。     

Photodegradation of estuarine dissolved organic matter: a multi-method assessment of DOM transformation

A multi-method approach was applied to study changes in dissolved organic matter (DOM) at three estuarine sites with varying salinity, as well as changes resulting from experimental photodegradation. Following measurement of ultraviolet and visible absorption spectra of bulk samples, DOM was isolated using C₁₈ solid phase extraction. The extract was characterized using high performance size exclusion chromatography (HP-SEC) and molecular level characterization was conducted via direct temperature-resolved mass spectrometry (DT-MS) and electrospray ionization mass spectrometry (ESI-MS). The molecular weight distribution of DOM as determined from HP-SEC and ESI-MS varied between techniques, but generally decreased down estuary and with photodegradation for both approaches. Relative differences in molecular weight were significantly correlated with the ratio of absorption coefficients at 254/365 nm. Additionally, photobleaching was significantly correlated with mass spectral characteristics from both DT-MS and ESI-MS. Principal component analysis of DT-MS spectra showed that photoexposure removed different mass spectral characteristics depending on sampling site; however, upon photodegradation, the mass spectral characteristics of both marine DOM and terrestrially dominated DOM approached a common spectrum. We interpret this spectrum, characterized by fragments from aromatic and carbohydrate-like precursors, as photochemically refractory DOM. Our results show that multiple approaches that characterize different aspects of DOM can provide complementary information about its sources and transformation. More specifically, photobleaching results in decreased light absorbance, decreased molecular weight and shifts in the relative abundance of classes of compounds (and broad shifts in m/z values); moreover, these transformations result in photodegraded samples from a low-salinity site which are compositionally similar to samples collected from a mid-salinity site further downstream.