Observations of high co rotational lines in post-AGBs and PN

We present a preliminary interpretation of high CO rotational line data obtained from KAO. The possibility of either a PDR or a shock model is considered in order to explain the observations.     

分子筛/石墨烯复合电极材料电化学性能的对比研究

利用溶液共混法制备得到分子筛/石墨烯(RGO)复合电极材料。比较了分子筛(4A、13X、SBA-15)种类、煅烧温度以及分子筛与氧化石墨烯(GO)质量比等因素,对分子筛/RGO复合电极材料电化学性能的影响。采用X射线衍射(XRD)、孔径分析、扫描电镜(SEM)和电化学测试等分析方法考察了3种复合电极材料的结构、形貌及电化学性能。结果表明,RGO可以将4A很好地包覆,且4A均匀镶嵌在RGO层间并阻止RGO团聚,形成了三维空间导电网络结构,13X、SBA-15并不能完全被RGO包裹,RGO层间团聚现象仍较严重,不能形成三维导电网络结构。当分子筛与RGO质量比为6∶1,煅烧温度为320°C时,在4 A/g电流密度下,4A/RGO复合电极材料的比电容为450 F/g,而相应的13X/RGO、SBA-15/RGO复合电极材料的比电容分别为195、43 F/g。4A/RGO复合电极材料优异的超级电容性能可归于4A与RGO之间较强的协同效应。     

不同沉积环境凝析油的分子有机地球化学特征

对中国１０个盆地不同沉积环境的４２个凝析油进行的ＧＣ、ＧＣ－ＭＳ、ＧＣ－ＡＥＤ及碳、氢同位素分析表明：海相、淡水、微咸水湖泊相、半成水湖泊相、咸水湖泊相凝析油以及沼泽相凝析油具有不同的有机分子和生物标记化合物组合以及碳氢同位素分布。海相凝析油富含异构烷烃和烷基环戊烷轻烃系列、硫芴及降姥鲛烷；贫二环倍半萜尤其是升锥满烷；Σ烷基环己烷／Σ正构烷烃值较大，具有较重的δＤ值和较轻的δ￣（１３）Ｃ值，前者平均－２９．８‰；后者平均－１１９．７‰。陆相咸水、半咸水湖相凝析油富含含硫化合物尤其是硫芴；Σ烷基环己烷／Σ正构烷烃值略小于海相凝析油；具明显植烷优势；具有较重的δ￣（１３）Ｃ值和δＤ值，平均值分别为－２５．５‰和－１２１．２‰，全烃色谱具继承性微弱奇偶优势。微咸水、淡水湖相凝析油相对富含二环倍半萜尤其是锥满烷和升锥满烷及芴。沼泽相凝析油富含甲苯、甲基环己烷（轻烃）、二环倍半萜及氧芴；尚检出有按叶油烷等陆相生标化合物；Σ烷基环己烷／Σ正构烷烃值较小，具有姥鲛烷优势；δ￣（１３）Ｃ值较重，平均值为－２６．５‰。     

岩石中微生物学研究的分子生物学技术——中国大陆科学钻探（CCSD）微生物研究

本文介绍了中国大陆科学钻探（CCSD）微生物学研究中所建立起来的分子生物学技术,即环境基因组DNA提取、16SrDNA分析、Real-timePCR技术和磷脂酸分析技术。另外探索了防污染的手段以及监测方法,并介绍了我们以这种方法对CCSD的微生物学研究所得到的一些初步结果。     

Acidic polar compounds in petroleum: a new analytical methodology and applications as molecular migration indices

A new method for analysis of acidic polar compounds, is described and discussed. It allows the simultaneous quantification of carboxylic acids, phenols and carbazoles and combines accuracy with a short turnaround time, a requirement strictly necessary for industrial applications. Routinely use of this methodology (more than 50 applications in many different sedimentary basins) has supplied many important pieces of information about oil origin, maturity, biodegradation and, in particular, has allowed to define a molecular migration index (MMI), based on relative abundance of phenol and alkyl phenols. The combination of well-established geochemical tools focused on saturated and aromatic fractions (such as biomarkers, compound specific isotope ratio analysis, and GC fingerprinting) with this methodology results in the definition of an integrated interpretative sequence. This last enhances the quality of interpretations through cross-checks and permits a better exploitation of oil samples by using also their less explored fraction, i.e. the polar compounds. Application results of this methodology are only shortly mentioned in this paper, which is mainly focused on analytical aspects. The results will be more extensively discussed in a future publication.     

黄颡鱼(Pelteobagrus eupogon)不同生态地理分布群体遗传多样性的微卫星分析

利用40个黄颡鱼微卫星分子标记对吉林省月亮湖野生黄颡鱼(YL,30尾)、四川野生黄颡鱼(SC,30尾)、黑龙江省哈尔滨市松花江段黄颡鱼(SH,18尾)、湖北省荆州市长湖野生黄颡鱼子代(YY,30尾)及其亲本(QQ,30尾)、天津市换新国家级原良种场黄颡鱼1号(TJ,30尾)6个黄颡鱼群体的观测杂合度(Ho)、期望杂合度(He)、多态信息含量(PIC)和有效等位基因数(Ae)等进行了遗传检测,根据基因频率计算遗传相似系数和Nei氏标准遗传距离,x2检验估计Hardy-weinberg平衡,采用近交系数(FST)和基因流(Nm)分析群体的遗传分化及其来源.同时,使用PHYLIP3.63软件绘制基于Nei氏标准遗传距离的UPGMA进化树.6个群体共检测到5042个扩增片段,长度在150-650bp,40个基因座扩增出等位基因数从1-8个不等,共计143个等位基因,平均每个基因座扩增得到3.575个等位基因.结果显示:(1)6个黄颡鱼群体的多态性指标均适中,PIC在0.00-0.79之间,平均值为0.40、0.37、0.35、0.39、0.35和0.19,有效等位基因数(Ae)1.00-5.44个不等,平均有效等位基因数依次为2.05、2.30、1.93、2.07、1.93和1.47,无偏期望杂合度(He)在0.00-0.83之间,平均值为0.45、0.46、0.36、0.46、0.41和0.23;(2)遗传相似系数YY与QQ遗传相似度最高(0.9947),TJ与SC遗传相似系数最低(0.4846),聚类结果与地理分布呈一定相关性.     

Tracing terrigenous dissolved organic matter and its photochemical decay in the ocean by using liquid chromatography/mass spectrometry

Reversed-phase liquid chromatography/mass spectrometry (LC/MS) is introduced as a new molecular fingerprinting technique for tracing terrigenous dissolved organic matter (DOM) and its photochemical decay in the ocean. DOM along a transect from the mangrove-fringed coast in Northern Brazil to the shelf edge was compared with mangrove-derived porewater DOM exposed to natural sunlight for 2–10 days in a photodegradation experiment. DOM was isolated from all samples via solid-phase extraction (C18) for LC/MS analysis. DOM in the estuary and ocean showed a bimodal mass distribution with two distinct maxima in the lower m/z range from 400 to 1000 Da (intensity-weighted average of 895 Da). Terrigenous porewater DOM from the mangroves was characterized by a broad molecular mass distribution over the detected range from 150 to 2000 Da (intensity-weighted average of 1130 Da). Polar compounds, i.e., those that eluted early in the reversed-phase chromatography, absorbed more UV light and had on average smaller molecular masses than the more apolar compounds.     

A novel high-resolution small ion spectrometer to study ion nucleation of aerosols in ambient indoor and outdoor air

An electrically based ion spectrometer is described, capable of measuring particle sizes and mobilities from molecular ions (small ions) to aerosol particles across a size range of 0.4 to 30 nm in diameter. It consists of a single cylindrical capacitor divided into three electrically insulated sections. The current arriving at the central section is measured by an electrometer and represents the ion flux over a known range of mobilities determined by the applied voltage. The applied voltage is scanned in steps to measure the ion fluxes over a large number of overlapping mobility ranges. The recorded signal and the response function of the instrument are unfolded using a maximum entropy procedure to give a high-resolution measured mobility spectrum. The maximum entropy approach offers a considerable improvement over traditional aspiration collectors and can approach the resolution of a drift tube system. In this way, the spectrometer successfully overcomes the diffusion limit to small ion resolution. Illustrative spectra are shown, demonstrating for the first time the presence of some resolved structure within the small ion spectrum at the highest mobilities. It is demonstrated that the actual mobility spectrum of small ions falls in the range 0.8–2.0 × 10⁻⁴ m² V⁻¹ s⁻¹. This represents a narrower range than that previously measured which is attributed to improved spectral resolution in the present work.     

土壤水溶性有机物吸着系数及其影响因素研究

测定了中国中、东部地区17种土类45个表土样品中水溶性有机物的吸着系数、分子量分布、腐殖酸含量、粘土含量以及土壤pH值，分析了水溶性有机物吸着系数的分布、地域分异和影响吸着系数的主要因素。结果表明，中国中、东部主要天然土壤类型A层水溶性有机物吸着系数在0．0014－0．0284L/g，中位数为0．0062L/g；研究区吸着系数具有自北向南和自西向东递降的一般趋势。水热的地域分异是影响土壤A层Ks地域分异的根本因素，pH和WSOC分子量分布是直接影响Ks值的两个重要因素。