细粒沉积物及其古地理研究进展与展望*

细粒沉积物特征及其古地理研究对含油气细粒沉积物的勘探开发、评价预测、工程技术设计等意义重大。近年来,细粒沉积物,尤其是含油气细粒沉积物研究的快速发展,带来了一系列新的研究领域。在讨论细粒沉积物的定义、分类与特征的基础上,通过分析细粒沉积的文献知识群,获取细粒沉积物、页岩研究等结构、热点与发展方向。国际上细粒沉积物研究主要关注微结构和成因机制,近年来主要在具有油气意义的特殊细粒沉积物--页岩研究方面取得关键进展,对页岩的研究过程可以分为以页岩表征为代表的主知识网络和以页岩气赋存、运移等构成的延伸知识网络。细粒沉积物古地理恢复方法丰富,适用性存在差异,但量化、多因素综合、数据集成与深度挖掘、人工智能化将是细粒沉积古地理恢复方法的方向。在含油气细粒沉积物的优选评价方面,需要对沉积物本身特征与控制影响因素展开精细研究,进而延伸出“更宏观”与“更微观”2个主要发展方向。     

深海沉积物分类与命名的关键技术和方案

对地质研究的对象进行科学合理的分类,是地学研究的重要内容之一.为建立科学合理、量化统一、操作简便的深海沉积物分类与命名方案,详细分析国内外深海沉积物分类与命名现状,深刻了解海洋沉积物组成与分布,深入研究深海沉积物的水深、平均粒径和粘土含量3项参数指标,通过分析涂片鉴定粘土、钙质生物、硅质生物这三者的含量、粒度和化学分析之间的差异,建立钙质生物、硅质生物与CaCO₃、生物SiO₂的量化关系,完成沉降法和激光法粒度分析资料的对比和校正,分析深海沉积物分类与命名的兼容性和可比性.在上述研究成果基础上,自主创新提出深海沉积物分类与命名方案及其关键技术.深海沉积物类型简分法把深海沉积物分为深海粘土、钙质软泥、硅质软泥、粘土-硅质-钙质软泥4类,它能满足一般性海洋地质调查要求,达到基本了解深海沉积物类型的目的,在兼容世界深海沉积物类型现状的同时,充分考虑到混合沉积物的存在.深海沉积物类型细分法在简分法基础上细分了16种沉积物,使分类与命名更加详细和全面,满足海洋地质详细调查研究的要求.深海沉积物分类与命名方案与浅海沉积物分类与命名比较,在图形、类型指标、种类数量、冠字冠名法、混合沉积物表示法、可操作性等方面具有可比性,使浅海到深海的沉积物分类与命名呈渐变和有机联系.      

Environmental impact of the former Pb–Zn mining and smelting in East Belgium

In the mining district of Plombières-La Calamine (East Belgium), extensive Pb–Zn mining activities resulted in an important contamination of overbank sediments along the Geul river. Moreover, a huge amount of heavy metals is stored in a dredged mine pond tailing, which is located along the river. In the dredged mine pond tailing sediments, Pb–Zn minerals control the solubility of Zn, Pb and Cd. Although Pb, Zn and Cd display a lower solubility in overbank sediments compared to the mine tailing pond sediments, elevated concentrations of Pb, Zn and Cd are still found in the porewater of the overbank sediments. The considerable ‘actual’ and ‘potential’ mobility of Zn, Pb and Cd indicates that the mine pond tailing sediments and the overbank sediments downstream from the mine pond tailing represent a considerable threat for the environment. Besides the chemical remobilisation of metals from the sediments, the erosion of overbank sediments and the reworking of riverbed sediments act as a secondary source of pollution.     

海洋沉积物的锌同位素地球化学及其应用

锌同位素体系是海洋地球化学研究的新示踪剂,应用于示踪海水中锌元素的来源及其运移过程.海洋沉积物作为锌元素重要的"源"与/或"汇",其锌同位素组成的研究有助于理解海洋锌元素的地球化学循环.海洋沉积物记录了海水组成的信息,可以反演古海水锌同位素组成的变化,前提是理解沉积物与海水之间的分馏.对海水及海洋不同储库锌同位素研究进行系统总结,包括河流输入、热液体系、不同类型海洋沉积物(如富碳酸盐的沉积物、陆源硅酸盐碎屑、硅质沉积物、铁锰结核、贫氧-缺氧沉积物)的锌同位素组成,阐述了海洋沉积物锌同位素组成变化在古气候、古环境重建以及古海洋学等领域的应用以及重要性.      

Sulphur,organic carbon and iron relationships in estuarine and freshwater sediments: effects of sedimentation rate

Concentrations of S, organic C and Fe were investigated in profiles of sediments from two estuarine systems in the SW of Western Australia. In marine-affected sediments, inorganic S dominates total S and concentrations of total S correlate with Fe and not with organic C. In freshwater sediments, organic S dominates total S and concentrations of total S correlate with organic C and not with Fe. Molar Fe/S ratios in the estuarine sediments decrease with increasing salinity and approach unity for marine conditions. Net accumulation rates of S in sediments were estimated with a numerical computer model, calibrated with published data on profiles of marine sediments for diffusion of SO²⁻₄, sedimentation rates and distributions of S. Measured depth-integrated reduction rates of SO²⁻₄ in the marine-affected estuarine sediments approach those obtained for Fe-limited marine conditions at similar rates of sedimentation. Measured concentrations of inorganic S in anoxic freshwater sediments fit a numerically calculated relationship between inorganic S and sedimentation rate.     

The distribution and source of organic matter in reservoir sediments

The bottom sediments of two reservoirs, one with significant river sediment input and one without, were analyzed for organic matter content. Lake Texoma sediments average 1.0% organic carbon, of which 0.26% organic carbon is deposited by the river sediments of the Red and Washita River deltas. In Fort Gibson reservoir, where there is minimal river sediment input, the organic carbon averages 1.2% and is deposited with a strong correlation to water depth (+0.9). There is a significant difference between the C/N ratio of Lake Texoma sediments (11.5) and Fort Gibson sediments (9.6). The higher C/N ratio is suggested to be a result of the larger input of terrestrial plant debris (with a high original C/N ratio) by the rivers draining into Lake Texoma and the relatively high resistance of the lignin material in the plant debris to decomposition in the reservoir sediments.     

Microbial metabolites and the reductive dissolution of manganese oxides: Oxalate and pyruvate

Microorganisms may participate in the reductive dissolution of Mn oxides in sediments either directly, by using Mn oxides as a terminal electron acceptor, or indirectly, through the production and excretion of reductants and other molecules that perturb the chemical conditions in sediments. If the latter process is predominant, it should be possible to calculate rates of Mn mobilization from sediments from a knowledge of the kinetics of the reductive dissolution reaction, once the structures and concentrations of reductants found in sediments are known.Laboratory experiments show that synthetic Mn (III, IV) oxides are reduced and dissolved by the microbial metabolites oxalate and pyruvate at appreciable rates. This provides additional evidence that indirect involvement of microbes in the mobilization of Mn in sediments can occur. Rates of reductive dissolution increase as the pH is decreased; the effect of pH on dissolution rate is more pronounced for oxalate than for pyruvate. Ways in which chemical conditions in freshwater and marine sediments affect rates of Mn mobilization are discussed.     

稳定湖相沉积物和风成黄土粒度判别函数的建立及其意义

沉积物粒度变化主要受搬运介质、搬运方式、沉积环境和气候等多种因素的控制,通过粒度分析可判别沉积物的成因类型,推断其形成的沉积环境,解释环境演变。利用统计学方法对典型稳定湖相沉积物（罗布泊湖相样品２８２块,岱海湖相样品１２３块）和典型风成黄土（甘肃兰州榆中样品２６３块）粒度参数进行定量化分析,并经稳定湖相和风成沉积物验证,获得稳定湖相与风成沉积物的判别公式:Ｆ（湖相、风成沉积物） ＝２０．３６３Ｍｚ－５６．３７１Ｓｄ－６７．９２２Ｓｋ＋２３．５１６Ｋｇ－５５．６２６,若Ｆ＞０,为稳定湖相沉积物,反之,Ｆ＜０,则为风成沉积物。这为研究地史中稳定湖泊与风成环境 沉积物的鉴别提供粒度分析定量化判别方法,它对陆相古环境、干旱化事件和尘暴事件等研究具有十分重要的借鉴价值。     

孟加拉湾东经90°海岭中上新世以来沉积记录及亚洲季风

利用古生物地层学、碳酸盐地层学、X射线粉晶衍射和粒度分析等方法对东北印度洋孟加拉湾东经90°海岭上的远洋沉积物进行了综合研究.在此基础上, 以陆源物质的粒度为切入点对该区的沉积作用、沉积物来源及其可能的搬运机制进行了探讨, 对过去有关研究区陆源物质的源区和搬运方式作了补充.陆源物质的粒度可作为东南季风或赤道东风的替代性指标, 其变化不仅反映源区的火山活动情况, 而且指示了风力的强弱.陆源物质的多少则主要取决于青藏高原和印度次大陆的剥蚀情况和地表径流的强弱.二者之间通过高原隆升及其引发的环境效应联系起来.      

Texture and geochemistry of the sediments of a tropical mangrove ecosystem,southwest coast of India

The textural and geochemical aspects of the sediments of a tropical mangrove ecosystem have been studied and discussed. The sediments are characterized by the abundance of silt and sand with minor amounts of clay. The mean size of the sediment ranges from 0.205 mm to 0.098 mm (fine to very fine grained sand). The sediments are very poorly sorted, negatively to very negatively skewed, and platy to extremely leptokurtic in nature. The organic carbon content of the sediments ranges from 0,33% to 4.93%, which is controlled by the particle size of the sediments. The CaCO₃ content is five times the enrichment of organic carbon. This enhanced CaCO₃ content of the mangrove sediments might be a result of the abundance of shell fragments in the sediments. The shell mining activities in the estuarine bed adjoining the Kumarakam mangroves also contribute a substantial amount of lime muds to the mangrove area, which in turn add CaCO₃ to the sediments. The relative concentrations of heavy metals are Fe > Mn > Cr > Zn > Ni > Cu. All heavy metals other than Fe show an increase in concentration compared to the other parts of the estuarine bed. Cluster analysis indicates that the contents of organic C, Fe and Mn have a marked bearing on the Cr, Zn, Ni, and Cu levels of the mangrove sediments.     

Comparison between the lower Nansi Lake and its inflow rivers in sedimentary phosphorus fractions and phosphorus adsorption characteristics

There were many differences between rivers and lakes such as flow velocity, hydraulic retention time, water vegetation community and other chemical-physical factors that may lead to different characteristics of sedimentary phosphorus. In our research, sedimentary phosphorus fractions and its phosphorus adsorption differences between the lower Nansi Lake and its main inflow rivers were compared. The results showed that the contents of NaOH-P, Org-P, IP-P, and TP in lake sediments were obviously higher than those in its inflow river sediments while HCl-P had no obvious difference between them. Based on analysis, the unstable NaOH-P would accumulate in lake sediments, while it is difficult for it to retain in sediments of rivers because of a high frequency of flood flows and unstable bed sediments. In addition, water vegetation communities were helpful in the accumulation of Org-P in lake sediments. From phosphorus adsorption experiments results, the Ceqc (equilibrium concentration of phosphorus release/adsorption) of lake sediments was higher than that of river sediments. It was indicated that sedimentary phosphorus would be more easily released from lake sediments than river sediments. So in future more work should be focused on internal P loading from lake sediments release.     

Role of prior exposure on anaerobic degradation of naphthalene and phenanthrene in marine harbor sediments

The anaerobic degradation of the polycyclic aromatic hydrocarbons (PAHs) naphthalene and phenanthrene was investigated in several marine harbor sediments. In sediments from Boston Harbor that were heavily contaminated with petroleum, [¹⁴C]-naphthalene and [¹⁴C]-phenanthrene were oxidized to ¹⁴CO₂ without a lag, suggesting that the microbial community was adapted for anaerobic PAH oxidation in situ. The addition of molybdate, a specific inhibitor of sulfate-reducing microorganisms, inhibited PAH mineralization which suggested that sulfate reducers were involved in the anaerobic oxidation of the PAHs. PAHs were also anaerobically oxidized at another site in Boston Harbor that was less heavily contaminated, but at a slower rate than in the most heavily contaminated sediments. Sediments not contaminated with petroleum did not significantly oxidize the PAHs. A similar correspondence between rates of anaerobic PAH oxidation and the degree of PAH contamination was observed in sediments from Tampa Bay and San Diego Bay. When relatively pristine sediments from San Diego Bay that did not have a significant capacity for anaerobic PAH oxidation were exposed to high concentrations of naphthalene, they developed a potential for naphthalene degradation that was comparable to that in sediments that had a history of PAH contamination. The increase in potential for naphthalene degradation in the sediments exposed to naphthalene was associated with an increase in naphthalene-degrading microorganisms. These results suggest that many marine harbor sediments contain microorganisms capable of anaerobically oxidizing PAHs under sulfate-reducing conditions and that these microorganisms will respond with an increase in their activity when PAHs are introduced into the sediments. Thus, if PAH inputs into harbor sediments from petroleum can be reduced there may be a widespread potential for microorganisms to remove this PAH contamination from the sediments, despite anaerobic conditions.     

地下咸水与水库水体交换过程中沉积物胶体释放规律

以天津滨海地区北大港水库为研究对象,采用室内柱试验,研究地下咸水与水库水体交换过程中不同位置沉积物胶体释放以及盐分释放/截留的动态特征,同时对沉积物胶体释放、盐分释放/截留机理进行了探讨。研究结果表明:水库不同位置地下咸水与水库水体交换过程中,盐分的归宿不同:接近水库入口处的沉积物能将盐分截留下来,而出水口沉积物却将盐分释放转移到水体。随孔隙体积数的增加,沉积物胶体累计释放量逐渐增加,入库口、库中心、出库口最大累计释放量分别为3.275 mg/g、0.386 mg/g和1.382 mg/g;胶体累计释放量随孔隙体积数的变化曲线符合直线型,胶体释放速率变化很小。盐分的释放或截留是沉积物颗粒的粒径、胶体含量、含盐量等多种因素作用的结果,水库水体与沉积物中的盐分处于动态平衡状态,当沉积物中含盐量高于平衡浓度时,其盐分会向水体中释放,同时吸附在胶体上的盐分也会随着胶体的释放而释放;反之,水体中的盐分会向沉积物中迁移被截留下来,沉积物粒径越小,越易吸附水中的盐分。胶体的释放规律可以用双电层理论得到很好的解释。     

太湖沉积物和湖岸土壤的污染元素特征及环境变化效应

太湖沉积物和湖岸土壤具有相似的物质组成，具有相同的物源，通过补给区的径流，营养元素和重金属元素随着土壤迁入湖泊，由于沉积物和土壤物化条件的不同，它们的营养元素和重金属含量有差异。土壤中氮，磷的总量和有效态均比沉积物中高，表明有一部分营养物质进入了水体；营养元素高的沉积物均靠近城镇，其原因为居民生活污水排放，土壤和沉积物中多数重金属元素尚未超过自然背景值，只有沉积物中Cd和Pb，土壤中的Cu,Cd和Hg超过，但沉积物中重金属元素大多比土壤中高，特别在北部沿岸沉积物中，重金属元素含量大大超过平均值，这种不正常的高值是由人类不合理的废水，废物敢排放引起。     

基于BP神经网络的稳定湖相和风成沉积物粒度数据表征方法

沉积物的形成受到多种地质因素的综合控制。通过粒度分析可判别沉积物的成因类型,推断其形成的沉积环境,解释环境演变;而沉积物的粒度组分除了受到原岩的控制外,还受到机械沉积作用的影响难以准确预测。运用人工神经网络对稳定湖相沉积物和风沉积物的粒度参数进行研究,将沉积物的4个粒度参数作为网络模型的输入变量,在对168个浙闽沿海迎风岸风成老红砂样品和282个苏贝淖湖滨湖泊沉积物样品所对应的粒度参数进行数据样本训练之后,获得了基于BP神经网络的稳定湖相和风沉积物预测模型。然后利用448个大树摆鱼湖相沉积物粒度参数样本和100个兰州榆中黄土风沉积物粒度参数样本作为测试样本对该模型进行了测试和验证,结果显示模型的可靠性较好,能够对沉积物的形成环境做出正确的判断。     

Spatial and temporal variations in terrestrially-derived organic matter from sediments of the Delaware estuary

Terrestrially-derived organic matter in sediments of the Delaware Estuary originates from riverine transport of soils and fresh litter, sewage and industrial wastes, and marsh export of organic matter. The quantity, composition, and spatial distribution of terrigenous organic matter in sediments was determined by elemental (C and N), lignin, and stable carbon isotope analyses. Sediments in the upper Delaware Estuary had low organic carbon content and high lignin content. In contrast, sediments in the lower Delaware Estuary had high organic carbon content and low lignin content. There was a slight decrease in the proportion of syringyl and cinnamyl phenols relative to vanillyl phenols between the upper estuary and lower estuary. Differences in lignin and stable carbon isotope compositions between sediments of the Delaware Estuary and sediments of the Broadkill River estuary (an adjoining salt-marsh estuary) supported previous observations that marshes do not export substantial quantities of organic matter to estuaries. Additional results suggested that lignin-rich sediments were concentrated in the upper estuary, most likely in the zone of high turbidity. Furthermore, algal material diluted lignin-rich sediments, particularly in the lower estuary. The weaker algal signal in bottom sediments compared to that in suspended particulate matter suggested algal material was decomposed either in the water column or at the sediment-water interface. Physical sorting of sediments prior to deposition was also indicated by observations of compositional differences between the upper and lower estuary bottom sediments. Finally, seasonal variations in primary productivity strongly influenced the relative abundance of terrestrial organic matter. In fall, however, the proportion of lignin was greatest because of a combination of greater inputs of terrestrially-derived organic matter, lower river discharge, and a decrease in algal biomass.     

Geological aspects of decomposition of corpses in mass graves from WW1 and 2, located in SE Poland

The investigations were carried out to identify processes and mineral products in the diversified subsoil sediments of mass graves from WW1 (four graves) and 2 (five graves) and their surroundings, as well as the relations between the development of sediments within the mass graves and the scale of migration of the products of corpse decomposition. The author studied the role of iron compounds and clay minerals in the decomposition of human corpses buried in mass graves, followed by the migration of selected elements. In particular, he concentrated on the list of elements found in the diversified sediments of nine mass graves from SE Poland and to their relationship with phosphorus compounds. The methods applied included scanning electron microscopy (SEM) and optical polarizing microscopy. Samples were collected from various depths in trenches and holes dug in the vicinity of the graves, the sediments from the burial horizon and, when possible, the sediments underlying the grave (studied downslope). Detected phosphorus occurs as a weakly crystalline compound in silt-rich sediments with relatively stable water conditions. In silt-rich sediments with relatively stable moisture content, phosphorus occurs as a weakly crystalline compound. More stable aggregates of decomposition products have been found on quartz grains covered with clay-ferruginous rims. Fragments of human soft tissue were found only in those graves from WW2. There is no link between the spectrum of elements in the sediments of the graves and the period of burials. The decomposition products that form depend primarily on the type of sediments in which the mass graves were dug and, secondarily, although related, on the moisture content of the sediments. It has been found that stabilization of decomposition products in situ is related to the presence of iron compounds and clay minerals, particularly in finer-grained, aleuritic–pelitic sediments.     

长江与黄河河口沉积物磁性特征对比的初步研究

根据2001年8月和9月分别采自黄河与长江河口沉积物样品的磁性测量和粒度分析,探讨长江和黄河河口沉积物的磁性特征及其差异。长江河口沉积物中亚铁磁性物质的含量高于黄河口,但长江口与黄河口沉积物中都是亚铁磁性矿物主导了样品磁性特征,亚铁磁性矿物晶粒都以假单畴-多畴为主。相比黄河口沉积物,长江口沉积物不完整反铁磁性物质对磁性特征的的贡献较小。长江与黄河河口的这种磁性特征主要反映了不同的沉积物来源的控制影响。此外,无论是长江口还是黄河口沉积物,磁性参数χARM、χfd%与沉积物细粒级组分存在显著的相关性,表明这两个参数作为粒度的代用指标具有普遍性。     

Diagenesis and very low-grade metamorphism of volcaniclastic sandstones from contrasting geodynamic environments, North Island, New Zealand: the Murihiku and Waipapa terranes

Abstract The Mesozoic Murihiku and Waipapa terranes are two accretionary wedges of linked forearc and trench sediments, respectively, that were juxtaposed in the early Cretaceous.
Late Triassic to late Jurassic Murihiku terrane volcaniclastic sediments are folded into a regional syncline and have been diagenetically altered. There is a general relationship between zeolite occurrence, clay mineralogy, vitrinite reflectance and stratigraphic position. Youngest Jurassic sediments contain heulandite, analcime and stilbite, whereas late Triassic to mid-Jurassic sediments have laumontite and heulandite (in detail the zeolite distribution is complicated). Tuffaceous horizons on the eastern limb of the syncline are calcitized rather than zeolitized. Post-diagenetic fractures associated with uplift are laumontite-filled. The inferred geothermal gradient is c. 15° C km⁻¹.
The Waipapa terrane is an accretionary complex dominated by imbricated terrigenous sediments of Triassic and Jurassic age with enclosed Permian to Jurassic pelagic sediments and basalts. Late Jurassic sediments are massive volaniclastic sandstones. The sediments are non-foliated, and metamorphic minerals in the massive sandstones have crystallized in specific domains. The observed metamorphic succession of prehnite-pumpellyite and pumpellyite-actinolite facies assemblages was overprinted in the imbricated rocks during a thermal event that was late in the deformation sequence and broadly coincident with hydraulic fracturing and veining.
The metamorphic successions in the two terranes and their relationships to structural features are in excellent accord with accretionary complex models.     

The effect of organic matter and oxygen on the degradation of bacterial membrane lipids in marine sediments

The biodegradation of purified radiolabelled membrane lipids from a methanogenic bacterium and a pseudomonad were investigated in mangrove, beach and high marsh marine sediments under aerobic and anaerobic conditions. The effect of organic matter on the amount and rate of degradation was also examined by supplementing beach sediments with humic acids. In aerobic sediments, CO₂ was the major product of lipid degradation while under anaerobic conditions both CO₂ and CH₄ were major end products and the overall rates were reduced (up to 40%) relative to aerobic conditions. Total bacterial numbers increased during all incubations with the largest increases occurring in anaerobic sediments supplemented with humic acids. No lipid degradation occurred in aerobic or anaerobic sediments treated with formaldehyde or autoclaving. In low organic beach sediments, the ester-linked phospholipid of the pseudomonad was degraded much more rapidly than the diphytanyl glycerol diether of the methanogen with 69% of the phospholipid degraded in 96 hours versus only 4% of the methanogen lipid. Lipid degradation in both aerobic and anaerobic sediments was highly correlated to organic matter content with increasing amounts of organic matter inhibiting degradation. Long incubations (75 days) of the diphytanyl glycerol ether resulted in 51% degraded to CO₂ in low (0.5%) organic mangrove sediments while only 9% was mineralized in high (10.8%) organic marsh sediments. Physicochemical sorption of membrane lipids to the organic matrix is proposed as a mechanism which protects membrane lipids from microbial attack and degradation.