Cr^3＋在改善三元复合驱中的作用实验研究

在三元复合驱矿场应用实践中,由于三元复合体系自身流度控制能力的局限性,必须通过聚合物凝胶前置段塞来改善吸液剖面,这就涉及到聚合物凝胶与三元复合体系的配伍性。通过向三元复合体系中加入有机铬,考察Cr^3＋对三元复合体系黏度、界面张力和阻力系数等性能影响,进而对Cr^3＋聚合物凝胶与三元复合体系配伍性以及Cr^3＋在改善三元复合体系性能方面的作用做出评价。结果表明,Cr^3＋的加入对三元复合体系黏度和界面张力影响不大,但阻力系数和残余阻力系数却明显增加。当采用Cr^3＋聚合物凝胶作为前置段塞或采用添加Cr^3＋的三元复合体系进行复合驱油实验时,其采收率增加幅度都要高于普通三元复合驱。这不仅显示出Cr^3＋聚合物凝胶与三元复合体系间良好的配伍性,而且为改善三元复合驱增油效果提供了新的途径。     

Kinetic and equilibrium studies of copper-dissolved organic matter complexation in water column of the stratified Krka River estuary (Croatia)

An interaction of dissolved natural organic matter (DNOM) with copper ions in the water column of the stratified Krka River estuary (Croatia) was studied. The experimental methodology was based on the differential pulse anodic stripping voltammetric (DPASV) determination of labile copper species by titrating the sample using increments of copper additions uniformly distributed on the logarithmic scale. A classical at-equilibrium approach (determination of copper complexing capacity, CuCC) and a kinetic approach (tracing of equilibrium reconstitution) of copper complexation were considered and compared. A model of discrete distribution of organic ligands forming inert copper complexes was applied. For both approaches, a home-written fitting program was used for the determination of apparent stability constants (K_i^equ), total ligands concentration (L_iT) and association/dissociation rate constants (k_i¹,k_i^- 1).A non-conservative behaviour of dissolved organic matter (DOC) and total copper concentration in a water column was registered. An enhanced biological activity at the freshwater–seawater interface (FSI) triggered an increase of total copper concentration and total ligand concentration in this water layer. The copper complexation in fresh water of Krka River was characterised by one type of binding ligands, while in most of the estuarine and marine samples two classes of ligands were identified. The distribution of apparent stability constants (log K₁^equ: 11.2–13.0, log K₂^equ:8.8–10.0) showed increasing trend towards higher salinities, indicating stronger copper complexation by autochthonous seawater organic matter.Copper complexation parameters (ligand concentrations and apparent stability constants) obtained by at-equilibrium model are in very good accordance with those of kinetic model. Calculated association rate constants (k₁¹:6.1–20 × 10³ (M s)^− 1, k₂¹: 1.3–6.3 × 10³ (M s)^− 1) indicate that copper complexation by DNOM takes place relatively slowly. The time needed to achieve a new pseudo-equilibrium induced by an increase of copper concentration (which is common for Krka River estuary during summer period due to the nautical traffic), is estimated to be from 2 to 4 h.It is found that in such oligotrophic environment (dissolved organic carbon content under 83 µM_C, i.e. 1 mg_CL^− 1) an increase of the total copper concentration above 12 nM could enhance a free copper concentration exceeding the level considered as potentially toxic for microorganisms (10 pM).     

Multivariate analysis of fluorescence and source identification of dissolved organic matter in Jiaozhou Bay, China

Hierarchical clustering analysis and principal component analysis (PCA) methods were used to assess the similarities and dissimilarities of the entire Excitation-emission matrix spectroscopy (EEMs) data sets of samples collected from Jiaozhou Bay, China. The results demonstrate that multivariate analysis facilitates the complex data treatment and spectral sorting processes, and also enhances the probability to reveal otherwise hidden information concerning the chemical characteristics of the dissolved organic matter (DOM). The distribution of different water samples as revealed by multivariate results has been used to track the movement of DOM material in the study area, and the interpretation is supported by the results obtained from the numerical simulation model of substance tracing technique, which show that the substance discharged by Haibo River can be distributed in Jiaozhou Bay.     

Impact of dynamic feedbacks between sedimentation,sea-level rise,and biomass production on near-surface marsh stratigraphy and carbon accumulation

Salt marshes accrete both organic and inorganic sediments. Here we present analytical and numerical models of salt marsh sedimentation that, in addition to capturing inorganic processes, explicitly account for above- and belowground organic processes including root growth and decay of organic carbon. The analytical model is used to examine the bias introduced by organic processes into proxy records of sedimentation, namely ¹³⁷Cs and ²¹⁰Pb. We find that accretion rates estimated using ²¹⁰Pb will be less than accretion rates estimated using the ¹³⁷Cs peak in steadily accreting marshes if (1) carbon decay is significant and (2) data for ²¹⁰Pb extend below the ¹³⁷Cs peak. The numerical model expands upon the analytical model by including belowground processes such as compaction and root growth, and by explicitly tracking the evolution of aboveground biomass and its effect on sedimentation rates. Using the numerical model we explore how marsh stratigraphy responds to sediment supply and the rate of sea-level rise. It is calibrated and tested using an extensive data set of both marsh stratigraphy and measurements of vegetation dynamics in a Spartina alterniflora marsh in South Carolina, USA. We find that carbon accumulation in marshes is nonlinearly related to both the supply of inorganic sediment and the rate of sea-level rise; carbon accumulation increases with sea-level rise until sea-level rise reaches a critical rate that drowns the marsh vegetation and halts carbon accumulation. The model predicts that changes in carbon storage resulting from changing sediment supply or sea-level rise are strongly dependent on the background sediment supply: if inorganic sediment supply is reduced in an already sediment poor marsh the storage of organic carbon will increase to a far greater extent than in a sediment-rich marsh, provided that the rate of sea-level rise does not exceed a threshold. These results imply that altering sediment supply to estuaries (e.g., by damming upstream rivers or altering littoral sediment transport) could lead to significant changes in the carbon budgets of coastal salt marshes.     

红树植物木榄叶中挥发油的化学成分

以正己烷为溶剂,采用回流提取法提取红树植物木榄叶中的挥发油,运用毛细管气相色谱-质谱联用技术分离检测得到40个峰,鉴定了其中的32种成分,被鉴定成分占挥发油总量的91.92%,其主要成分为烷烃类(30.31%)、萜类化合物(25.22%)、芳香化合物(14.07%)、酸(10.60%)、酯(5.36%)和烯(3.49%).     

川东板东构造长兴组生物礁及其地震特征研究

根据板东构造板东4井等长兴组钻探资料,对长兴组的生物礁进行了研究。研究表明板东构造长兴组储集岩有生物（屑）泥晶灰岩-含生物（屑）泥晶灰岩、礁灰岩和白云岩。综合储集岩物性特征、区域钻、测井资料及野外剖面,总结了生物礁的形成与演化模式及模式各部位所对应的岩性和物性。通过地震响应特征、反演等技术建立了长兴组储层识别模式,利用对应速度、Landmark属性提取的储层有效厚度经计算机网格化编制出了长兴组储层厚度分布预测图,与钻测井厚度对比,证实板东4井生物礁为点礁。     

基于卫星遥感的南海海域POC浓度时空变化特征研究

海水中颗粒有机碳(POC)是海洋碳循环的基本变量,在海洋碳循环研究中起着关键作用。根据2003—2020年南海区域遥感数据反演的POC数据集,分析了南海海域POC浓度时空变化规律。研究结果表明:在整个研究区POC的年平均浓度变化范围为76.98~83.91 mg/m^(3);POC浓度分布呈现出近岸高、远海低,主要原因为南海近岸浅水海域POC浓度主要受陆源输入和沿岸流影响,远海区域内POC浓度主要受南海环流和水团控制。在季度上,第1—4季度POC浓度平均值为89.62,72.90,79.22,84.86 mg/m^(3);总体上POC浓度呈现出夏季低、冬季高的趋势,主要原因为南海受到冬季的东北季风和夏季的西南季风影响,影响到南海海水混合层的结构变化,浮游植物在冬季比夏季更为繁盛。在月尺度上,1月POC浓度平均值达到最高值;2—4月POC浓度平均值快速下降,5月POC浓度平均值达到最低值;6—12月POC浓度平均值开始缓慢上升。以上研究结论可为南海碳循环、政府碳达峰、碳中和及应对气候变化等提供决策依据。     

南黄海陆架中部沉积物反射率光谱的影响因素分析

利用Minolta CM-2002光谱光度计对南黄海陆架136个短柱样品20~25cm段的沉积物进行了颜色反射率数据测量,通过化学元素、粒度、磁化率等来确定影响沉积物颜色反射率变化的成分和因素,介绍了反射率光谱的一阶导数和因子分析的方法。分析结果表明,南黄海陆架沉积物颜色反射率受控于沉积物中的铁氧化物、有机质以及粘土矿物和钙质生物碎屑含量。主因子F1指示氧化环境,并与陆源物质相关,F2指示弱氧化环境,F3指示弱还原环境,主因子的波长范围分别是405~445 nm和495~595 nm,605~695 nm,445~485 nm。     

海三棱藨草(Scirpus mariqueter)根系低分子量有机酸对根际沉积物重金属生物有效性的影响

应用等离子光谱仪(ICP)与高效液相色谱仪(HPLC)分别对海三棱藨草根际沉积物中重金属(Cu、Pb、Zn和Cd)不同化学形态含量和植物根系分泌物中常见低分子量有机酸进行了季节跟踪测定,分析了有机酸(柠檬酸、草酸、酒石酸、苹果酸、甲酸和乳酸)含量与重金属化学形态(可交换态、碳酸盐结合态、铁锰氧化物结合态、有机结合态和残渣态)的季节相关性。结果表明,柠檬酸、草酸和苹果酸含量与Cu和Pb的除残渣态外的其它4种形态含量呈正相关性,表明其能提高Cu和Pb生物有效性,与Zn的所有形态含量呈负相关性,降低了生物有效性;酒石酸、甲酸和乳酸含量与Cu和Pb的可交换态含量呈负相关性,而与其它形态含量相关性不明显,降低了生物有效性。与Zn的除残渣态外的其它4种形态含量呈正相关性,提高其生物有效性。而上述所有有机酸与Cd的各种化学形态相关性不明显。表明其对Cd的生物有效性影响不大。