海洋真菌及其生物活性物质多样性研究

海洋微生物种类繁多,是筛选新药的丰富资源宝库。近些年来,作为海洋微生物中重要的组成部分的海洋真菌正成为研究的热点,越来越受到国内外学者的关注。本文详细概述了海洋真菌的定义、分布、海洋真菌研究的历史和现状、其所产生的生物活性物质多样性以及存在的问题。     

The petroleum generation potential and effective oil window of humic coals related to coal composition and age

A worldwide data set of more than 500 humic coals from the major coal-forming geological periods has been used to analyse the evolution in the remaining (Hydrogen Index, HI) and total (Quality Index, QI) generation potentials with increasing thermal maturity and the ‘effective oil window’ (‘oil expulsion window’). All samples describe HI and QI bands that are broad at low maturities and that gradually narrow with increasing maturity. The oil generation potential is completely exhausted at a vitrinite reflectance of 2.0–2.2%R_o or T_max of 500–510 °C. The initial large variation in the generation potential is related to the original depositional conditions, particularly the degree of marine influence and the formation of hydrogen-enriched vitrinite, as suggested by increased sulphur and hydrogen contents. During initial thermal maturation the HI increases to a maximum value, HI_max. Similarly, QI increases to a maximum value, QI_max. This increase in HI and QI is related to the formation of an additional generation potential in the coal structure. The decline in QI with further maturation is indicating onset of initial oil expulsion, which precedes efficient expulsion. Liquid petroleum generation from humic coals is thus a complex, three-phase process: (i) onset of petroleum generation, (ii) petroleum build-up in the coal, and (iii) initial oil expulsion followed by efficient oil expulsion (corresponding to the effective oil window). Efficient oil expulsion is indicated by a decline in the Bitumen Index (BI) when plotted against vitrinite reflectance or T_max. This means that in humic coals the vitrinite reflectance or T_max values at which onset of petroleum generation occurs cannot be used to establish the start of the effective oil window. The start of the effective oil window occurs within the vitrinite reflectance range 0.85–1.05%R_o or T_max range 440–455 °C and the oil window extends to 1.5–2.0%R_o or 470–510 °C. For general use, an effective oil window is proposed to occur from 0.85 to 1.7%R_o or from 440 to 490 °C. Specific ranges for HI_max and the effective oil window can be defined for Cenozoic, Jurassic, Permian, and Carboniferous coals. Cenozoic coals reach the highest HI_max values (220–370 mg HC/g TOC), and for the most oil-prone Cenozoic coals the effective oil window may possibly range from 0.65 to 2.0%R_o or 430 to 510 °C. In contrast, the most oil-prone Jurassic, Permian and Carboniferous coals reach the expulsion threshold at a vitrinite reflectance of 0.85–0.9%R_o or T_max of 440–445 °C.     

In-situ Formation of Light-Absorbing Organic Matter in Cloud Water

Current climate models seem to underestimate the flux of solar energy absorbed by the global troposphere. All of these models are constrained with the assumption that cloud droplets consist of pure water. Here we demonstrate in a simple laboratory experiment that aromatic hydroxy-acids which are found in continental fine aerosol can react with hydroxyl radicals under typical conditions prevalent in cloud water influenced by biomass burning. The reactions yield colored organic species which do absorb solar radiation. We also suggest that the products of such reactions may be humic-like substances whose presence in continental aerosol has been confirmed but their source mechanisms are still much sought after. We also attempt to give a first order estimate of the enhancement of water absorption at a visible wavelength under atmospheric conditions.     

Organic pollutants associated with macromolecular soil organic matter: Mode of binding

A study of ether-linked moieties in macromolecular bound residues of polycyclic aromatic hydrocarbons (PAH) generated in bioremediation experiments was performed using high temperature hydrolysis degradation with subsequent analysis of the products by GC-MS. This hydrolysis reaction was specifically designed to cleave ether bonds including relatively stable diarylether structures. Among the reaction products, aromatic alcohols representing typical microbiologically derived metabolites of PAH were found in addition to natural compounds. Thus, parts of the bound residues appeared to be linked within the macromolecular material by ether bonds. Model experiments with an oxidoreductase enzyme and aromatic alcohols indicate the formation of these ether bonds to be an enzyme-catalysed process.     

关于侵入岩体中金矿床成因研究若干问题的讨论

各时代、不同类型侵入岩中的金矿床是金矿的主要类型。关于金矿床与岩体的成因关系目前尚存在不同的看法，但传统的岩浆热液成因观点仍居统治地位，其原因往往在于不少研究者把岩液热液成因当成了固定模式应用于具体矿床的研究，而不是建立在综合研究的基础之上。本文结合近年来金矿的研究进展，强调侵入岩中金矿床的研究的研究要综合考虑成岩成矿的时代与时差，成矿流体和成矿物质的来源等各方面因素。金矿床定年的进展研究表明，矿     

药用滑石粉酸中可溶物测定方法考察

考察药用滑石粉酸中可溶物测定方法的重复性、耐用性 ,分析主要影响因素。比较酸溶物提取液滤过介质对测定结果差异的影响 ;采用重量法随机测定酸溶物含量和室间差异。两种滤过介质处理对测定结果没有显著差异 ;室间测定结果没有显著差异 ;30批样品平行测定结果的 RSD值范围为 0 %～ 18.2 %。酸中可溶物测定法存在重复性和耐用性不佳的问题 ,应相应调整酸中可溶物含量限度     

Transformation of arsenic compounds in modern intertidal sediments of Iriomote Island, Japan

The arsenic accumulation process in intertidal sediments of Iriomote Island, Japan, is analyzed as a naturally balanced arsenic-fixation system. Major and minor element chemistry is analyzed by X-ray fluorescence photometry, mineralogy is investigated by X-ray diffractometry, and four arsenic compounds are characterized by hydrogen-generated atomic absorption photometry. It is found that arsenic is accumulated by iron hydroxides/oxides precipitated following the decomposition of humic acids in the shallower sediment, and is subsequently incorporated into iron sulfide minerals at depth. The arsenic is immobile during incorporation into arsenic-bearing phases, suggesting that arsenic is unlikely to be released into the porewater under natural conditions in early diagenesis. The formation and decomposition of arsenic-bearing organic compounds appear to be associated with the formation and decomposition of arsenic in oxyhydroxides/oxides, suggesting that microbial activity may play an important role in controlling the behavior of arsenic and arsenic-bearing phases in the sediment column.     

Cu2+对序批式反应器中活性污泥胞外聚合物产量及其组分的影响

研究了长期暴露条件下Cu2+对序批式反应器(SBR)性能及其活性污泥胞外聚合物(EPS)特性的影响。结果表明,进水中加入10 mg·L-1的Cu2+后,在SBR运行的第16~55天,COD和NH+4-N的去除率保持稳定;在第56~75天,COD和NH+4-N的平均去除率与进水Cu2+浓度为0 mg·L-1时相比分别下降了3.88%和6.41%。浓度为10 mg·L-1的Cu2+长期作用下,活性污泥中EPS、松散附着EPS(LB-EPS)和紧密附着EPS(TB-EPS)产量及LB-EPS和TB-EPS中蛋白质(PN)含量增加。傅里叶变换红外光谱分析表明10 mg·L-1 Cu2+的长期暴露导致TB-EPS中PN的C=O键、N-H键和C-O键相对含量降低。X射线光电子能谱(XPS)测试结果显示在10 mg·L-1 Cu2+长期暴露条件下,LB-EPS和TB-EPS中元素Cu和O百分含量增加。     

河口物质和水体长期输运分离的理论分析和观测验证 Ⅰ.物质和水体长期输运分离的理论分析

基于单宽断面潮周期平均水体和物质对流输运通量,定义了二维水体和物质长期输运速度,它们分别描述单宽断面水体和物质长期输运的方向及快慢。通过二维水体和物质长期输运速度的对比分析,提出了物质和水体长期输运分离概念:受物质浓度影响,在物质和水体瞬时运动速度相同的情况下,物质和水体潮周期平均对流输运的方向和快慢可能存在差异。本文将二维物质长期输运速度分解为二维水体长期输运速度、二维潮泵输运速度和垂向切变输运速度,它们分别描述余流输运、潮泵输运和垂向切变输运,后两种输运造成单宽断面物质和水体长期输运分离。本文的分析表明,河口受地形、径流、潮流、密度梯度影响,存在有利于物质和水体长期输运分离的自然条件。     

三种海洋硅藻胞外多聚物形态、微细结构及组成的初步研究

利用光镜和扫描电镜对厦门近海三种常见附着硅藻——爪哇曲壳藻亚缢变种(Achnanthes javanica var．subconstricta)、咖啡形双眉藻(Amphora coffeaeformis)和多枝舟形藻(Nav-icula ramosissima)胞外多聚物(Extracellular polymeric substances,EPSs)的形态和微细结构进行了研究,并初步分析了其化学组成。结果表明,A．javanica var．subconstricta的胞外多聚物为透明的长柄,分为领、柄及垫状物三部分,电镜显示其徽细结构为由许多纤维组成的双层实心管;Amphora coffeaeformis分泌的EPS为由串连的小节组成的实心管状结构,许多管交织成厚的胶质块;Navicula ramosissima的EPSs则为透明的薄膜并形成胶质膜。三种硅藻胞外多聚物的水溶性和水不溶性的主要成分均为多糖类,达总量的70％以上,蛋白质含量次之．不含脂类物质,但不同藻类EPS的组成差异较大。此外,还探讨了EPSs的功能及其分泌机理。