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。     

Pretreatment of high strength waste emulsions by combined vibratory shear enhanced process with Fenton oxidation

Pretreatment of waste emulsions with high organic content by a combined process of vibratory shear enhanced process and Fenton’s oxidation prior to biological treatment was investigated. Vibrating membrane had shown good performance in chemical oxygen demand and oil removals and the mitigation of concentration polarization. However, the permeate after filtration processing still contained high content of organics. Thus, additional Fenton oxidation was applied to reduce the organic loading, and improve the biodegradability of the wastewater. The optimal molar ratio of ferrous iron to hydrogen peroxide was 0.05 obtained from the jar-test experiments. Removal of organics was enhanced by increasing hydrogen peroxide dosage, while efficiency of hydrogen peroxide reached maximum of 1.11(w/w) at the hydrogen peroxide dosage of 6.8 g/L. Furthermore, the biological experiments indicated that the high concentration of organics could inhibit microbial activity, which decreased the chemical oxygen demand degradation rates. The adaptive period of the microbe was greatly shortened using Fenton’s reagent at the low dosages. The improvement of the biodegradability could be explained by partial mineralization and chemical transformation of parent organic compounds after Fenton oxidation.     

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.     

近40年来气候变化对青海盐湖及其矿产资源开发的影响——以小柴旦湖为例

青海是中国盐湖主要分布区之一,蕴藏着丰富的矿产资源。文章以RS和GIS技术为基础,从20世纪70年代、90年代、2000年前后、2008~2009年和2013~2014年五期Landsat遥感影像中提取了青海面积大于10 km2的所有盐湖(不包括干盐湖),分析了其近40年来的变化趋势:总体上,盐湖总面积除在2000年前后有所减少外,基本上呈现增加的趋势;具体而言,2000年前后,萎缩的盐湖主要分布在柴达木盆地;其他时期均呈现全面扩张的趋势。在全球气候变暖的大背景下,通过分析青海地区11个气象台站的年平均气温、年降雨量和蒸发量数据,可知青海地区气候呈现了向暖湿方向转型的趋势,且2002年之后更为明显。最后,以青海省小柴旦湖为例,分析了湖泊淡化、矿产资源贫化对盐湖资源开发的影响,具体为:1资源开发成本升高、难度加大,甚至使一些处于工业开发临界品位的盐湖失去开发价值;2盐湖淡化条件下,锂等矿产资源有效提取技术亟待研发;3政府制定矿产资源开发政策时,需要对气候及盐湖的动态变化过程综合考虑。以上说明,青海地区的暖湿气候使盐湖大幅度淡化,给盐湖矿产资源开发带来了新的挑战。     

柴达木盆地西部油族划分及成因研究

对柴达木盆地西部各油田的151个原油进行了分子地球化学分析,并选取伽马蜡烷/C30藿烷、升藿烷指数、甾烷C27/C29和三环萜烷/C30Hop四个参数作为变量进行SAS聚类分析。结合常规二维散点图法,柴西原油可以分为3个油族7个亚族：油族Ⅰ以强水体分层、强还原环境为特征,主要分布于西端的七个泉、红柳泉地区,该油族可以分为两个亚族,油亚族②相比于油亚族①具有更高的甾烷 C27/C29比值;油族Ⅱ主要分布于狮子沟、花土沟、跃进和南翼山油泉子地区,在七个泉、红柳泉等地区也有分布,以相对较强的水体分层、还原环境为特征;油族Ⅲ主要分布于东（南）部的切克里克、乌南、绿草滩、咸水泉、跃西和跃进Ⅱ号等地区,以水体分层变差、较还原环境为特征,该油族可以分为3个亚族,其中油亚族⑤则具有异常低的三环萜烷/C30Hop 比值,油亚族⑥具有异常高的甾烷 C27/C29比值,油亚族⑦则具有异常高的三环萜烷/C30Hop 比值。油族空间分布特征受下干柴沟组源岩有机相在空间上的变化制约,下干柴沟组源岩发育时期,自西向东地层沉积速率增大,水体的分层变差、还原性降低,导致陆源输入的增加以及有机质保存条件变差。     

西秦岭成矿带中东段金矿床成矿规律和找矿预测

西秦岭近年来在新区发现新矿床和新类型金矿,矿床的地质特征表明金矿成矿受岩性、构造、岩浆活动的制约,许多金矿的地质、地球化学特征显示成矿与岩浆岩在时间和空间上关系密切;分析认为金矿主成矿时间为印支晚期-燕山早期,与区域大规模的岩浆活动在时间上一致;金矿主要有夕卡岩型、热液脉型和与岩浆活动有关的微细浸染型三种类型。矿石矿物元素组合显示由北而南成矿深度变浅、剥蚀程度较低;根据金、汞、锑矿床点和金、砷、锑、银元素分布特征,认为在北带岩体旁侧应注意寻找夕卡岩型和热液脉型金矿,中、南矿带在已知矿床深部注意寻找热液脉型金矿,有锑、汞矿点的区域注意深部及外围金矿的找矿;通过分析,最后圈定18处下一步重点工作区。     

西秦岭岷-礼成矿带岩浆活动与金矿成矿模式探讨

岷-礼成矿带发现较多大型金矿,同时在岩体内发现斑岩型钼矿。金矿床矿石中除有低温矿物外,还有黄铜矿、白钨矿等中-高温矿物,白钨矿在寨上金矿中是载金矿物之一;钼矿中也有黄铜矿、白钨矿矿物;金、钼、钨矿化分带有一定空间关系;金矿床地球化学、稳定同位素、放射性同位素和流体包裹体的研究表明成矿物质,成矿流体有深源特征;中川岩体群的岩石学、年代学、岩石化学、微量元素、稀土元素特征表明岩体为复式岩体,具有壳幔混源特征;据此建立成矿带内受印支-燕山期岩浆活动控制的金矿成矿模式。