鄂北致密薄储层地震响应特征分析

鄂尔多斯盆地北部大牛地气田塔巴庙区块致密薄层发育。利用岩石物理等数据的物性参数,对不同储集条件下的薄层、薄互层进行地震正演分析。结果表明:在薄层特别是薄互层条件下,叠前波场响应特征十分复杂,有别于常规AVO类型的变化规律,且含气层和干层的响应特征有明显差异。根据叠前地震波场的响应特征和不同的变化规律可以细化薄层研究,进一步识别储集类型。     

GPS技术在西贾庄-罗集铁矿项目中的应用

全球定位系统GPS(GlobalPositimingSystem),以其连续、实时、高精度、全天候测量和自动化程度高等优点,对经典大地测量学的诸多方面产生了极其深刻的影响,在与物化探测量相关的控制测量及测网布设中的应用也越来越广泛。该文通过一个物探项目中GPS测量整体方案的设计与实践过程,针对GPS控制测量、RTK测量、手持GPS测量几种作业方法的探讨及对相关数据的分析,概括总结了GPS技术应用于地勘项目的若干特点。     

延庆规划新城软弱粘性土工程特性研究

延庆规划新城存在大面积的软弱粘性土,严重影响了新城土地工程能力。本文主要针对新城地层结构及沉积演化特点,对软弱粘性土的物质成分、微结构特征以及土的物理力学参数等进行了分析,研究了该地区软弱粘性土各项参数之间的相关性,建立了多组参数间的线性回归方程,为日后规划新城大规模的建设,提供了工程地质参考和依据。     

黔北务川—正安—道真地区下二叠统大竹园组和梁山组孢粉学研究

文中材料采自黔北务川—正安—道真地区下二叠统大竹园组和梁山组。大竹园组孢粉化石类型单调,保存较差;而梁山组孢粉化石丰富,保存良好。孢粉组合特征为:(1)大竹园组包含丰富的Calamospora和Florinites及少量Torispora verrucosa,Gulisporites,Alisporites,Hamiapollenites和Striatopodocarpites,这一孢粉组合主要出现在上石炭统至下二叠统。按照大竹园组层位和孢粉化石特征,其地质时代应为早二叠世Asselian期—Artinskian期(相当于紫松期—隆林期)。(2)梁山组中可建立孢粉组合Laevigatosporites vulgaris-Gulisporites-Florinites ovalis,共计发现孢粉化石34属49种,其中蕨类植物孢子含量为51.6％～56.1％,裸子植物花粉含量为43.9％～48.4％。与大竹园组沉积时期相比,这一时期植被极为繁盛。根据孢粉组合特征,梁山组地质时代可能为早二叠世隆林期,即Kungurian期。     

中国及邻区印支运动特征及其意义

通过概要论述印支运动在中国及邻区的表现特征,探讨了印支运动的主要成矿作用,指出印支运动首次使长期以来游离于全球主要大陆外的扬子、中朝、塔里木等小陆块拼合在一起,为新生代大型聚煤盆地的形成奠定了基础,也为燕山期和喜马拉雅山期二次大规模的对流地幔输入大陆事件奠定了重要基础,使之成为中国及邻区大陆上最重要的成矿时期。     

Investigating soil thermodynamic parameters of the active layer on the northern Qinghai-Tibetan Plateau

The soil thermodynamic parameters, including thermal conductivity, diffusivity and volumetric capacity within the active layer on the northern Tibetan Plateau, were calculated using the measured data of soil temperature gradient, heat flux, and moisture at four stations from October 2003 to September 2004. The results showed that the soil thermodynamic parameters exhibited clear seasonal fluctuation. The thermal conductivity and diffusivity in summer and autumn at Beiluhe, Kexinling, and Tongtianhe were larger than those in winter. The volumetric thermal capacity causes an opposite change; it was larger in autumn and winter than in summer. In spring, the soil thermal conductivity at the Kekexili station was larger than that in summer. Generally, fine-grained soils and lower saturation degrees in the topsoil might be a reason for the lower soil thermal conductivity in winter. For a given soil, soil moisture was the main factor influencing the thermodynamic parameters. The unfrozen water content that existed in frozen soils greatly affected the soil thermal conductivity, whose contribution rate was estimated to be 55 %. The thermodynamic parameters of frozen soils could be expressed as a function of soil temperature, volumetric ice content and soil salinity, while for the unfrozen ground the soil moisture content is the dominant factor for those thermal parameters. As for the soil thermal diffusivity, there exists a critical value of soil moisture content. When the soil moisture content becomes less than a critical value, the soil thermal diffusivity increases as the soil moisture content rises.     

Controlling factors of the δ 11B-pH proxy and its research direction

Significant boron isotope fractionation occurs in nature (?70 ‰ to +75 ‰) due to the high geochemical reactivity of boron and the large relative mass difference between ¹⁰B and ¹¹B. Since the 1990s, reconstruction of ancient seawater pH using the isotopic composition of boron in bio-carbonates (δ ¹¹B_carb), and then calculation of the past pCO₂ have become important issues for the international isotope geochemistry community, and are called the δ ¹¹B-pH proxy. Although many achievements have been made by this proxy, various aspects of boron systematics require rigorous evaluation. Based on the previous researches, mechanism of boron isotope fractionation, variation of boron isotope (δ ¹¹B) in nature (especially in bio-carbonates) and controlling factors of the δ ¹¹B-pH proxy, such as the dissociation constant of B(OH)₃ in seawater (pK_a), the δ ¹¹B of seawater (δ ¹¹B_SW), the boron isotopic fractionation factor between B(OH) ₄ ^? and B(OH)₃ (α _4–3), and the incorporated species of boron into bio-carbonates, are reviewed in detail and the research directions of this proxy are proposed. Generally, the controversy about pK_a, δ ¹¹B_sw, and α _4–3 is relatively less, but whether boron incorporated into bio-carbonates only in the form of B(OH) ₄ ^? remains doubtful. In the future, it is required that the physicochemical processes that control boron incorporation into carbonates be rigorously characterized and that the related chemical and isotopic fractionation be quantified. It is also necessary and important to establish a “best-fit empirically equation” between δ ¹¹B_carb and pH of seawater based on the precipitation experiments of inorganic or culture experiments of corals or foraminifera. In addition, extended application of the δ ¹¹B-pH proxy to the earlier part of the Phanerozoic relying on the Brachiopods is worthy of studying. Like other geochemical indicators, there are limiting factors of δ ¹¹B; however, it remains a very powerful tool in the reconstruction of past seawater pH at present.     

Surface characterization of maize-straw-derived biochars and their sorption performance for MTBE and benzene

Biochars generated at various temperatures might show significant differences in sorption for organic contaminants. In this study, a series of biochars, generated from pyrolyzing maize straws at different temperatures, were systematically characterized. The characterization results showed that with increasing pyrolysis temperature, the surface areas, micropore areas and aromaticity of biochars were enhanced. Batch experiments were conducted to study methyl tert-butyl ether (MTBE) and benzene sorption to biochars. The results indicated that the sorption capacity of benzene to biochars was higher than that of MTBE. The higher pyrolyzed temperature of biochars resulted in a stronger sorption affinity for target compounds, and the dominant sorption mechanisms varied for biochars pyrolyzed at different temperatures. The sorption to biochars pyrolyzed at 700 and 800 °C performed a high adsorption capacity, which indicated that they might be a promising sorbent to remove MTBE and benzene from water. Biochar pyrolyzed at 400 °C showed transitional sorption mechanisms from partition to adsorption for MTBE and benzene. Pore-filling was a possible sorption mechanism to biochars pyrolyzed at high temperature.