BTEX anomalies used as indicators of submarine oil and gas reservoirs

It is a conventional method for petroleum prospecting to generally use paraffin hydrocarbon as basic indexes of oil and gas. This conventional geochemical technology, however, shows some limits in the prospecting as paraffin is vulnerable to influences from human and biologic activities. Consequently, BTEX (short for benzene, toluene, ethyl benzene and xylem, which are direct biomarkers) among aromatic hydrocarbon series has been taken into account for the oil and gas prediction. Domestic and foreign study results demonstrate that BTEX is hardly disturbed and can well indicate oil and gas reservoirs. Based on measured data from a South China Sea area, the present authors have used self-developed visual assessment software for petroleum prospecting has been used to process data, strip background anomalies, and outline significant BTEX anomalies. By comparison with stratigraphic profiles of the target area, it is confirmed that BTEX is a good indication of marine oil and gas during the petroleum prospecting.     

壳聚糖硫酸酯金属配合物的抗氧化活性

以吩嗪硫酸甲酯-NADH为超氧阴离子自由基(O_2~(·-))产生、检测体系和EDTANa_2-Fe(Ⅱ)-H_2O_2为羟自由基(~·OH)产生、检测体系,对壳聚糖硫酸酯铜、锌配合物和不同分子质量壳聚糖进行了抗O_2~(·-)和~·OH自由基的活性研究.结果表明,壳聚糖硫酸酯金属配合物对于O_2~(·-)自由基的清除能力明显高于壳聚糖,在质量浓度为0.025 g/L时,壳聚糖硫酸酯铜配合物对O_2~(·-)自由基的清除能力达到94.18%,壳聚糖硫酸酯锌配合物达到93.19%;壳聚糖硫酸酯铜、锌配合物对~·OH自由基的清除能力(67.39%、60.46%)低于相同分子质量的壳聚糖(88.06%),而高于高分子质量壳聚糖761 ku(18.71%);壳聚糖分子质量大小对O_2~(·-)和~·OH自由基的清除能力有较大影响,质量浓度为1.6 g/L壳聚糖分子质量为20 ku时,对O_2~(·-)清除率达54.69%,而分子质量在761 ku时,对O_2~(·-)清除率仅为35.50%;各样品对O_2~(·-)和~·OH自由基的清除能力均随着质量浓度的增加而上升,壳聚糖硫酸酯铜、锌配合物在相当低的浓度下(0.025 g/L)就可以达到明显清除O_2~(·-)自由基的效果(≥90%).     

涠洲岛潮滩表层沉积物中重金属的空间分布及其环境质量评价

根据2006年4月对涠洲岛潮滩表层沉积物的调查资料,分析了表层沉积物中重金属元素Hg、Cu、Pb、Zn、Cd、Cr、As的含量水平及空间分布特征,运用单因子评价法对其环境质量进行了评估,并通过相关性分析、因子分析探讨了几种重金属元素的物源.结果表明:涠洲岛潮滩环境质量状况良好,各元素均未达到污染水平,多数地区存在Cu的玷污,个别地区存在As的玷污;各分析元素较多的累积在人为活动相对频繁的XKZ、W05断面附近区域;Hg、Cu、Zn、Cr显著正相关,以环境背景来源为主,Pb、As较多的受到人为因素的影响.     

Impacts of soil fauna on litter decomposition at different succession stages of wetland in Sanjiang Plain, China

Litter decomposition is the key process in nutrient recycling and energy flow. The present study examined the impacts of soil fauna on decomposition rates and nutrient fluxes at three succession stages of wetland in the Sanjiang Plain, China using different mesh litterbags. The results show that in each succession stage of wetland, soil fauna can obviously increase litter decomposition rates. The average contribution of whole soil fauna to litter mass loss was 35.35%. The more complex the soil fauna group, the more significant the role of soil fauna. The average loss of three types of litter in the 4mm mesh litterbags was 0.3–4.1 times that in 0.058mm ones. The decomposition function of soil fauna to litter mass changed with the wetland succession. The average contribution of soil fauna to litter loss firstly decreased from 34.96% (Carex lasiocapa) to 32.94% (Carex meyeriana), then increased to 38.16% (Calamagrostics angustifolia). The contributions of soil fauna to litter decomposition rates vary according to the litter substrata, soil fauna communities and seasons. Significant effects were respectively found in August and July on C. angustifolia and C. lasiocapa, while in June and August on C. meyeriana. Total carbon (TC), total nitrogen (TN) and total phosphorus (TP) contents and the C/N and C/P ratios of decaying litter can be influenced by soil fauna. At different wetland succession stages, the effects of soil fauna on nutrient elements also differ greatly, which shows the significant difference of influencing element types and degrees. Soil fauna communities strongly influenced the TC and TP concentrations of C. meyeriana litter, and TP content of C. lasiocapa. Our results indicate that soil fauna have important effects on litter decomposition and this influence will vary with the wetland succession and seasonal variation. Foundation item: Under the auspices of State Key Development Program for Basic Research of China (No. 2009CB421103), Key Program of National Natural Science Foundation of China (No. 40830535/D0101), Knowledge Innovation Programs of Chinese Academy of Sciences (No. KZCX2-YW-BR-16, KSCX2-YW-N-46-06)     

Application of matter-element model in soil nutrient evaluation of ecological fragile region

On the basis of the soil environment investigation in Da'an City, Jilin Province, China, 40 soil samples from main land use types were obtained and tested by standard method. Soil organic matter (SOM), total N (TN), total P (TP), total K (TK), available N (AN), available P (AP) and available K (AK) were chosen as the evaluation factors. A regional soil nutrient evaluation model was developed based on the matter-element model. The results show that the soil samples with nutrient grade Ⅱ-Ⅴ respectively account for 10%, 30%, 32.5% and 27.5%, and those with grade Ⅳ and Ⅴ account for 60% in all samples. The relationship between soil nutrients and land types indicates that the nutrients of farmland are relatively good, with 41.7% of soil samples with the nutrient grade Ⅳ and Ⅴ. The nutrients of saline-alkali land and sandy land are the worst, with 100% of soil samples with the nutrient grade Ⅳ and Ⅴ. And the ratios of soil samples grade Ⅳ and Ⅴ in grassland and wasteland are respectively 62.5 % and 54.55%. Generally speaking, the soil nutrients status in Da'an City is poor, 60% of soil samples are in poor and extremely poor conditions, indicating that the soil has been severely eroded. Being a relatively superior evaluation method with more accurate resuits and spatial distribution consistency, matter-element analysis is more suitable for regional soil nutrient evaluation than previous models.     

远源细粒辫状河心滩坝演化与河流分叉的交互沉积过程:现代沉积启示与数值模拟分析

远源细粒辫状河广泛发育于河流的中下游，其形成的致密储层是深入挖潜油气面临的挑战。结合现代远源细粒辫状河演变的遥感记录影像，运用基于泥沙水动力学的沉积过程数值模拟软件Delft3D正演远源细粒辫状河的生长演化过程，并探讨物源供给对远源细粒辫状河形态的影响，深入剖析和解释远源细粒辫状河心滩坝演化与河流分叉的交互作用和沉积过程，并进行了现代沉积验证。研究表明:①河道沿下游方向由窄变宽是触发远源细粒辫状河形成的主要地形条件。河流流速和河岸牢固程度是决定河流宽度的重要因素。②远源细粒辫状河心滩坝演化与河流分叉的交互沉积过程是心滩坝泥沙与河流流水交互作用的沉积演化过程。心滩坝泥沙与河流流水交互作用具体包括泥沙在河流中的沉积作用和河流对泥沙的侵蚀作用。③远源细粒辫状河心滩坝演化与河流分叉的交互沉积过程包括3种:河道内心滩坝加积导致河流分叉、心滩坝与河岸分离导致河流分叉、心滩坝的局部冲裂分解导致河流分叉。该研究丰富了远源细粒辫状河沉积理论，并且有助于分析远源细粒辫状河沉积相的储层空间展布规律并应用于油气的深入勘探开发。      

新疆阿克苏典型山前洪积扇内高氟地下水的化学特征及氟富集机制

在内陆干旱区,作为重要饮用水源的地下水常面临氟含量超标问题。查明内陆干旱区高氟地下水的分布规律,了解氟在地下水中的富集过程及其影响因素,既可丰富高氟地下水的研究体系,也是保证内陆干旱区饮水安全的重要基础。以新疆阿克苏地区典型山前洪积扇——依格齐艾肯河-喀拉玉尔滚河河间地带为研究区,基于水文地球化学调查结果,刻画了高氟地下水的分布区;结合氟离子含量与特征性水化学指标间的关系,揭示了高氟地下水的成因机制。结果表明:①地下水中氟含量的变化范围为0.8~6.1 mg/L,83%的水样氟含量超过《生活饮用水卫生标准》（GB 5749-2006）规定的上限（1.0 mg/L）;②总体上,氟含量沿地下水流动路径逐渐增大,低氟地下水（ρ（F-）≤1.0 mg/L）分布在国道314以北的补给区,高氟地下水（ρ（F-）>1.0 mg/L）分布在国道314以南的径流区和排泄区;③高氟地下水的水化学类型以Cl·HCO₃-Na型为主,而低氟地下水则以Cl·SO₄-Na型为主,高氟地下水相比于低氟地下水优势阴离子偏向于HCO₃-;④地下水的pH值范围为7.9~8.9（均值为8.4）,表明其处于弱碱环境中。地下水中ρ（F-）与pH值呈正相关,此外构成浅层含水层的上更新统沉积物中含有黑云母、氟磷灰石等矿物,其表面存在一定数量的可交换F-,这表明水中OH-与矿物表面F-间的阴离子交换可能对氟的富集有一定贡献;⑤地下水的F-含量与Ca2+含量呈负相关,即高氟地下水中ρ（Ca2+）小于低氟地下水。考虑到氟化钙（CaF₂）是自然界中的主要含氟矿物,也是地下水中氟的主要来源,ρ（F-）与ρ（Ca2+）间的这种负相关指示着高氟地下水中可能存在去Ca2+、Mg2+作用,如阳离子交替吸附或碳酸盐岩沉淀等。研究区地下水样中ρ（F-）与ρ（Mg2+）间也呈负相关关系,且和ρ（F-）与ρ（Ca2+）间的关系高度相似,也佐证了高氟地下水中去Ca2+、Mg2+作用的存在;⑥绝大部分地下水样品都位于氯碱性指数图的负值区域,且ρ（F-）与CAI-1和CAI-2均呈较好负相关,CAI-1和CAI-2都随ρ（F-）的增大而减小,这表明高氟地下水中存在Ca2+、Mg2+与Na+间更强的交换作用,对氟富集起着重要作用。地下水中ρ（F-）与SAR间呈较好正相关关系,且高氟地下水样的SAR均值（5.71）远大于低氟地下水SAR均值（1.67）,这也进一步证明高氟地下水中的Ca2+、Mg2+与含水介质的Na+间存在强烈的交替作用,对氟的富集起着重要作用;⑦所有地下水样中的萤石均处于未饱和状态,且萤石的饱和指数（SI）与F-含量间呈现较好的正相关,这表明地下水对含氟矿物（主要是萤石）的持续溶解应是导致研究区地下水中氟富集的主要原因。与之相反,研究区所有地下水样中的方解石均处于过饱和状态（SI>0）。这表明CaCO₃的沉淀可能促进了CaF₂的溶解,导致地下水中氟离子质量浓度增高;⑧研究区低氟地下水的δ18O值介于-11.20‰~-10.67‰间,平均值为-10.94‰,而高氟地下水的δ18O值介于-11.65‰~-11.21‰间,平均值为-11.49‰,即低氟地下水较高氟地下水富集δ18O。此外,F-质量浓度较低（ρ（F-）≤3.0 mg/L）的地下水样中δ18O值与F-质量浓度呈负相关,即低氟地下水具有更正的δ18O值;F-质量浓度较高（ρ（F-）≥4.8 mg/L）的地下水样中δ18O值与F-质量浓度的相关性不显著,随F-质量浓度的增高,δ18O值基本维持不变。以上表明蒸发浓缩作用对地下水中氟的富集贡献较小;⑨研究区地下水中ρ（F-）/ρ（Cl-）比值与ρ（F-）间呈现正相关,即ρ（F-）/ρ（Cl-）比值随ρ（F-）增高呈增大趋势,这也说明地下水中氟富集的主要原因是含氟矿物的溶解,而不是蒸发浓缩作用。此外,Gibbs图也提供了证据:研究区地下水样基本处于水岩作用主导区域,表明地下水化学特征（包括氟的富集）主要受水岩作用控制,蒸发浓缩影响很小。总之,地下水中氟的富集主要由溶解作用引起,OH-与矿物表面F-间的交换也有贡献,但蒸发浓缩作用影响微弱。含氟矿物持续溶解的驱动机制是阳离子交替吸附（地下水中Ca2+与岩土颗粒表面Na+之间）及方解石沉淀所引起的地下水中Ca2+的衰减。      

利用水系沉积物高程定量恢复古地貌的技术方法——以鲁西白彦地区白彦砾岩为例

主要分析了构造抬升对水系和地形的影响和恢复,以从古生代灰岩围岩中大面积但零星出露的岩溶砾岩点为研究对象,对区域古水系和地形地貌恢复和反演做出了新的尝试。在收集资料和实测的基础上,尝试性探讨了利用稳定水体参照物高程反演抬升高度以及邻区山峰点的古高程、古水系,恢复区域上古地形地貌的技术方法。并以白彦地区为例,通过白彦岩溶砾岩的分布、产状、金刚石矿物含量、岩性等地质特征,恢复白彦地区古地形线、古水系位置和流向等古地理地貌,指出在白彦期时代,该区总体发育4个水系,邹城市大石墙水系、枣庄水系、平邑水系、费县水系,水系中金刚石含量较为丰富的砾岩点大多分布在凤凰山隆起中心,其中在平邑水系推测存在一个山地峡谷中的古湖泊。认为蒙山凸起中已知的常马庄地区的金伯利岩脉所含有金刚石可能主要供应平邑区水系,其他3个地区水系的金刚石可能来源于凤凰山及其东部隆起剥蚀地区。     

南极放线菌NJ-F2萃取物的抗菌活性初步研究

从南极第24次科学考察采集的海泥样品中分离获得放线菌NJ-F2,对NJ-F2发酵液的乙酸乙酯萃取物进行体外抗菌实验,并采用16S rDNA方法对NJ-F2进行系统发育分析.结果表明萃取物对金黄色葡萄球菌和枯草芽孢杆菌的最低抑菌浓度(MIC)、最低杀菌浓度(MBC)分别为0.25 mg/mL,5.0 mg/mL;而对大肠杆菌和产气杆菌的MIC、MBC分别为0.5 mg/mL,5.0 mg/mL,但对真菌没有抗菌作用;16SrDNA分析结果表明NJ-F2为链霉菌属(Streptomyces sp.).     

羧甲基壳聚糖金属配合物的制备及抗O_2~-·活性研究

制备了羧甲基壳聚糖(CMCS)的3种金属配合物CMCS-Zn(Ⅱ),CMCS-Ca(Ⅱ)和CMCS-Ce(Ⅲ),通过红外光谱分析对其进行了表征,并对它们对超氧阴离子自由基O_2~-·的抑制作用作了研究.结果表明,在0.004～0.02 g/L浓度范围内,CMCS自身具有一定的O_2~-·抑制作用,且随浓度的增加而增大;CMCS-Ce(Ⅲ),CMCS-Ca(Ⅱ),CMCS-Zn(Ⅱ)_3种金属配合物对O_2~-·的抑制作用较CMCS有了一定提高,且抑制率亦随配合物浓度增加而增大;其中CMCS-Zn(Ⅱ)配合物催化O_2~-·歧化的活性最强,CMCS-Ca(Ⅱ)配合物次之,CMCS-Ce(Ⅲ)配合物最弱,说明配合物对O_2~-·的抑制作用与金属离子的种类有关.