冀北—辽西早白垩世沉积有机质特征与古气候环境演变

本文对冀北—辽西地区早白垩世沉积盆地富有机质沉积岩进行了初步有机地球化学分析研究。结果显示,冀北—辽西沉积盆沉积有机质特征在时间和空间上存在很大差异,代表白垩系早期沉积的滦平盆地大北沟组有机质丰度低,这不仅显示其所代表的沉积相带不利于有机质的聚集,也反映了当时生物不够繁盛;大店子组时期沉积相带发生了变化,有机质类型随着发生了变化,丰度有所增高,但总体上显示环境条件不利于生物的发育和繁盛。到了桥头组和义县组沉积岩有机质丰度大幅升高,表明生物界非常繁盛,古气候环境有利于有机质的大量生成和堆积,总体上反映了温湿的气候条件;但同时也存在较为频繁或交替性寒冷气候波动,具体的古气候环境状态尚需进一步深入研究。     

A 16 ka climate record deduced from δ^13C and C/N ratio in Qinghai Lake sediments, northeastern Tibetan Plateau

1 INTRODUCTION δ13C in organic matters from lacustrine sedi- ments varies with several factors including aquatic plants, vegetation type in the catchment, atmos- pheric CO2 concentration, climate (temperature and precipitation), and properties of water, …     

有机显微组分X射线衍射分析方法在油气评价中的应用

Ｘ射线衍射分析法适宜于分析有机显微组分的芳环层的层状结构。有机质的芳环层结构与其类型和演化程度有关。表征有机质芳环层的层状结构的主要参数：高度Ｌｃ、宽度Ｌａ、网面间距ｄｈｋ１和芳环层层数可作为油气勘探中判断源岩性质、类型、演化程度与生烃潜力的依据。文章还对参数的变化与意义进行了初步讨论。     

云南金顶铅锌矿床的有机成矿作用——来自围岩、矿石中有机质生物标志化合物的证据

云南金顶铅锌矿床是世界上成矿时代最新且唯一的陆相沉积岩容矿的超大型铅锌矿床。矿区存在2类有机质——原生型和迁移型,与矿石共生。生物标志化合物研究结果表明：正构烷烃碳数分布范围较宽,有2种峰型;萜烷化合物的相对丰度五环三萜烷＞三环萜烷＞四环萜烷;规则甾烷C27～C28～C29呈不对称V字型分布;有机质的母质来源以低等水生生源的海藻类为主,伴随有一定量的陆源高等植物组分;有机质沉积于弱氧化—弱还原环境;成矿热液的热力作用使样品遭受了一定程度的热解,部分样品还遭受了生物降解作用;生物标志物多参数对比表明有机质来源于三叠纪三合洞组碳酸盐岩地层。原生型有机质的成矿作用主要体现在对成矿金属元素的预富集上,而迁移型有机质的成矿作用主要是对成矿金属元素的活化运移。     

Chemical Characteristics of Carbonaceous Aerosols During Dust Storms over Xi＇an in China

Characterization of carbonaceous aerosols including CC (carbonate carbon), OC (organic carbon), and EC (elemental carbon) were investigated at Xi'an, China, near Asian dust source regions in spring 2002. OC varied between 8.2 and 63.7 μg m-3, while EC ranged between 2.4 and 17.2 μ m-3 during the observation period. OC variations followed a similar pattern to EC and the correlation coeflcient between OC and EC is 0.89 (n=31). The average percentage of total carbon (TC, sum of CC, OC, and EC) in PM2.5 during dust storm (DS) events was 13.6%, which is lower than that during non-dust storm (NDS) periods (22.7%). CC, OC, and EC accounted for 12.9%, 70.7%, and 16.4% of TC during DS events, respectively. The average ratio of OC/EC was 5.0 in DS events and 3.3 in NDS periods. The OC-EC correlation (R2=0.76, n=6) was good in DS events, while it was stronger (R2=0.90, n=25) in NDS periods. The percentage of water-soluble OC (WSOC) in TC accounted for 15.7%, and varied between 13.3% and 22.3% during DS events. The distribution of eight carbon fractions indicated that local emissions such as motor vehicle exhaust were the dominant contributors to carbonaceous particles. During DS events, soil dust dominated the chemical composition, contributing 69% to the PM2.5 mass, followed by organic matter (12.8%), sulfate (4%), EC (2.2%), and chloride (1.6%). Consequently, CC was mainly entrained by Asian dust. However, even in the atmosphere near Asian dust source regions, OC and EC in atmospheric dust were controlled by local emission rather than the transport of Asian dust.     

陆相湖盆海侵事件对烃源岩发育影响机制

海侵是影响湖盆烃源岩发育的重要事件之一,通过调研国内外相关文献,述评了这一领域的研究现状。海侵事件广泛分布于中国的松辽盆地、渤海湾盆地和苏北盆地以及国外多个盆地,海侵可通过古遗迹标志、矿物岩石学标志以及地球化学特征等识别。其次海侵烃源岩一般具有有机质丰度较高、有机质类型较好的特征,主要归因于海侵事件明显促进烃源岩发育,海侵作用一方面可能为湖水带来了大量的营养物质,显著提高了古湖泊生产力,另外一方面,盐度可能有利于形成稳定的水体分层,在水底形成强还原环境,促进有机质保存。以西非裂谷盆地（Termit盆地）为例,总结了海侵影响湖相烃源岩发育的模式。     

Trace metal composition of colloidal organic material in marine environments

Marine colloidal material (1 kDa–0.2 μm) was isolated by cross-flow ultrafiltration followed by diafiltration and freeze-drying from surface waters of the Gulf of Mexico and the Middle Atlantic Bight (MAB), as well as from estuarine waters of Galveston Bay. Elemental characterization of isolated colloidal material included organic carbon (OC) and selected trace metal (Cu, Pb, Zn, Cd, Co, Ni, Cr, Be, Fe, Al, Mn, V, Ba, and Ti) determinations. It was found that levels of these metals in marine colloids ranged from <0.1 to 50 μg/g colloidal matter, except for Fe which generally had a concentration >120 μg/g. Most metals (Cu, Pb, Zn, Ni, Al, Mn, V, and Ti) had an average concentration >1 μg/g while concentrations of Cd, Co and Be were usually <1 μg/g. Metal concentrations (μg/g) in isolated colloids were, in general, higher in Galveston Bay than in the Gulf of Mexico, suggesting either high abundance of trace metals in estuarine waters or differences in organic matter composition. Higher colloidal metal concentrations in the MAB than in the Gulf of Mexico might be due to higher terrestrial inputs in the MAB. Colloidal metal concentrations (μg/g) were generally lower than those in average soils, continental crust and suspended particles. However, metal/aluminum ratios (Me/Al) in isolated marine colloids were significantly higher than those for average soils and continental crust. Most importantly, colloids had a metal composition and metal/OC ratio (Me/C) similar to humic substances and marine plankton, suggesting that marine colloids largely originate from planktonic sources and are composed of predominately organic components. The Me/C ratios of Galveston Bay colloids followed the sequence of Cu>Ni, Cr, Zn>Mn>Co>Pb, Cd, which is similar to the Irving–Williams order except for Mn, suggesting that the interaction of metals with marine colloids is determined by the affinity of metals for specific organic ligands.     

大河影响下的边缘海沉积有机碳输运与埋藏及再矿化研究进展

大河影响下的边缘海是陆源输入物质的主要储库,也是有机碳埋藏和再矿化的主要场所,在全球碳的生物地球化学循环中有着重要作用。从有机碳的输运、埋藏和再矿化等方面综述了大河影响下的边缘海沉积有机碳生物地球化学研究的最新进展。研究表明,有机碳的来源、组成、粒径和密度分布等显著影响着有机碳的分布特征和归宿,大河影响下的边缘海中移动泥等特殊沉积环境在有机碳的输运、埋藏和再矿化分解等方面发挥了独特的作用;微生物分解作用则是边缘海沉积有机碳,特别是难降解陆源有机碳发生分解的重要因素。综合运用分子生物学、有机地球化学、生物地球化学等多学科研究手段,深入研究特定微生物、浮游生物功能类群等在大河影响下的边缘海沉积有机碳生物地球化学过程中的作用,将极大地丰富对河口和陆架边缘海生源要素生物地球化学循环的认识。     

九龙江口水体中1995年有机物的转移

1995年3个航次调查研究结果表明,九龙江口水体总有机物的含量受悬浮物含量控制。在S＜5的低盐度区,悬浮泥沙和有机物产生明显的絮凝沉降;在S＞5的广阔海域,它们的迁移接近于理想混合。估算得出九龙江河流的入海通量约：悬浮泥沙为9．8×105t／a;总COD为3．2×104t／a,其中溶解态COD为2.1×104t／a,约占2／3,为水体有机物的主要形态,如换算为溶解有机碳,则DOC的平均通量为3．2×104t／a。     

Photochemical production of molecular hydrogen in lake water and coastal seawater

Samples of lake water and coastal seawater from Nova Scotia, Canada, were irradiated with natural or artificial sunlight to investigate the potential for photochemical hydrogen production. Hydrogen photo-production was observed in all natural water samples. Rates of hydrogen formation were highest in coloured lake water (range: 98–163 pmol L^− 1h^− 1) and lower in seawater (range: 19–45 pmol L^− 1 h ^− 1). Dilutions of the most highly coloured lake sample (Kejimkujik Lake) showed a positive linear relationship between H₂ production rates and CDOM concentration. Photo-production rates normalised to UV absorption coefficients at 350 nm indicated that the photochemical efficiency of hydrogen formation varied between samples, perhaps due to differences in the CDOM composition. Photochemical hydrogen formation was also seen in solutions of syringic acid and acetaldehyde: two low-molecular-weight carbonyl compounds found in natural waters. Photochemistry may therefore offer least a partial explanation for the persistently high levels of hydrogen observed in the low-latitude surface ocean.