新型复合胶无粘土冲洗液研究及应用

针对松散覆盖层、强风化破碎层取心率低,岩心松散破碎,孔壁稳定性差等问题,进行了以天然植物胶为主原料的处理剂复配改性研究和冲洗液优化配方研究。主要研究方法是通过有机聚合物和无机交联剂的作用,对羟丙基瓜尔胶(GRJ)进行交联改性,以此获得新型复合胶无粘土冲洗液优化配方,并进行了现场应用。应用效果表明,该冲洗液密度低,粘度可调范围大,流变性和润滑性好,成膜护心、护壁作用强,完全满足第四系覆盖层、胶结差的砂卵石层和强风化破碎地层取心钻进要求。      

长江口潮滩沉积物－水界面无机氮交换通量

对长江口滨岸潮滩7个典型断面三态氮的界面交换通量进行了三年多的季节性连续观测,结果表明无机氮的界面交换行为存在复杂的空间分异和季节变化。NO^-₃-N和NH⁺₄-N的界面交换通量正负变化范围较大,分别介于-32.82~24.13 mmol.m^-2.d^-1和-18.45~10.65mmol.m^-2.d^-1之间;而NOsup>-₂-N的界面交换通量很小,仅为-1.15~2.82 mmol.m^-2.d^-1。NO^-₃-N的界面交换具有明显的上下游季节性时空分异特征,而NH⁺₄-N的界面交换则表现为南北岸季节性时空分异现象。盐度是控制长江口滨岸潮滩NH⁺₄-N界面交换行为的主要因素,而沉积物粒度、水体 NO^-₃-N浓度、沉积物有机质含量、水温和溶解氧含量则以不同的组合方式,共同制约着 NO^-₃-N在潮滩界面交换的时空分异格局。     

黑龙江省达连河油页岩地球化学特征及成因探讨

论述了达连河含煤段油页岩及油页岩段油页岩的地球化学特征,探讨了两套油页岩成因。这两套油页岩地球化学性质有很多相似之处,主要表现为油页岩都属于中熔或难熔的硅质灰分,SiO₂、Al₂O₃及Fe₂O₃含量很高;无机元素 Mn/Ti小于0.1,Sr/Ba为0.1～0.5,V/Ni为2.6～7.0;有机质类型以腐泥腐殖型为主,正构烷烃OEP值为1.55～3.67,具奇碳数优势,主峰碳为nC₂₃和C₂₉,Pr/Ph比值平均高达2.30,具强烈的姥鲛烷优势,Pr/nC₁₇比值为1.18～3.20,说明这两套油页岩都形成于淡水、近岸及弱氧化-弱还原的湖沼相沉积环境。但含煤段油页岩沉积时期高温、湿润的古气候条件下的喜湿植物面貌,使油页岩母质类型具有较多的富氢组分,这是造成两套油页岩品质差异的主要原因。     

表面活性剂的应用研究—：——动力学光度法测定痕量硒蹄

研究了表面活性剂在Ｓｅ和Ｔｅ诱导反应中的作用,对反应机理进行了初步探讨。实验表明,在选定条件下,加入适量非离子表面活性剂Ｔｗｅｅｎ－８０,使Ｔｅ的诱导反应速度加快,灵敏度提高１倍,并利用其对Ｓｅ有抑制反应速度的作用,使Ｔｅ对Ｓｅ的抗干扰能力增强。阴离子表面活性剂十二烷基苯磺酸钠对Ｓｅ和Ｔｅ均有加速反应的作用,Ｓｅ的灵敏工提高１．３倍：Ｔｅ的灵敏主提高４０％。基于此,所建立的中用于地质样品中纳克级Ｓ     

中国若干下寒武统高硒地层的有机地球化学特征及生物樗物研究

通过中国若干下寒武统高硒地层的有机地球化学及生物标志物研究,主伙高硒地层中有机质的先质母体为菌藻类生物,某些生物樗物指标指示了沉积环境为封闭的缺氧环境。同时,文章结合地质实际讨论还原的沉积环境有利于菌藻类生物的生长和保存,硒的富集与菌藻生物的繁盛有关。     

COMPARATIVE STUDIES OF INORGANIC CARBON UTILIZATION IN EMILIANIA HUXLEYI AND SOME NON-CALCIFYING MARINE MICROALGAE

INTRODUCTIONMarinemicroalgaeacquiretheirinorganiccarbonforphotosynthesisfromseawaterwhereinorganiccarbonmaybepresentasfreeCO2 ,H2 CO3andHCO-3 andCO2 -3 .TheproportionsofdifferentDICformsareprimarilyrelatedtopH ,andtotemperatureandsalinitytoalessextent.ThetotalDICisashighas2mmol Linseawa terbutthisismainlyintheformofHCO-3 .InnormalpHrangeof7.8-8.2inseawater,HCO-3 accountsfororethan 90 %ofthetotalDIC,whilefreeCO2 islessthan1 % .TheequilibriumconcentrationoffreeCO2 isonly1 2 μm…     

自生片钠铝石的碳氧同位素特征及其成因意义

自生片钠铝石的碳氧同位素特征可以为片钠铝石的成因研究提供重要的地球化学依据。以海拉尔盆地乌尔逊凹陷和松辽盆地孤店构造片钠铝石碳氧同位素分析为基础,结合国内外已报道的自生片钠铝石的碳氧同位素数据,对自生片钠铝石的碳氧同位素特征及其成因意义进行了探讨。研究表明,海拉尔盆地乌尔逊凹陷和松辽盆地南部孤店CO2气田砂岩中片钠铝石的δ13C范围分别为–5.3‰～–1.5‰（PDB）、–1.9‰～+0.3‰（PDB）,均分布于含无机碳物质δ13C分布区间（－9.0‰～＋2.7‰）内。计算出的海拉尔盆地和松辽盆地与片钠铝石平衡的CO2气碳同位素分布范围分别为－10.7～－7.0‰（PDB）、－8.7～－6.9‰（PDB）,表明片钠铝石绝大部分形成于无机CO2背景。实际地质观察中形成片钠铝石的CO2绝大多数为岩浆脱气来源,岩浆成因片钠铝石碳同位素分布范围为－5.5～＋4.5‰（PDB）。海拉尔盆地和松辽盆地的片钠铝石是岩浆成因CO2气运移、聚集的特征矿物。计算出的海拉尔盆地和松辽盆地片钠铝石沉淀时介质水的δ18O值范围为-14.3～-9.4‰（SMOW）,表现为轻同位素的特点,表明片钠铝石形成时地层水为大气降水。计算出的海拉尔盆地片钠铝石同位素为52.7～93.6℃,与样品所在深度处的古地温范围（65.4～87.6℃）基本吻合。     

酸雨对桂林枯水期岩溶地下水δ13CDIC及碳汇效应的影响

定量评价硫酸对岩溶碳汇效应的影响有助于提高岩石风化碳汇通量估算精度, 对当前全球气候变化研究意义重大.选取受酸雨影响的桂林岩溶区为研究对象, 在枯水期对研究区14个岩溶大泉和15条地下河水化学成分和碳同位素进行了测试分析, 结果表明: 岩溶大泉和地下河中阳离子以Mg2+和Ca2+为主, 阴离子以HCO₃-为主, 分别占阳离子和阴离子组成的90%以上, SO₄2-含量较低, 其含量范围为0.004~0.213mmol/L; 所占阴离子组成比例为0.12%~6.11%;δ13C_DIC、[Ca2++Mg2+]/[HCO₃-]更偏向于碳酸溶解端元, 离硫酸溶解端元距离远, 证实硫酸参与碳酸盐岩的溶解对地下水无机碳(dissolved inorganic carbon, 简称DIC)及δ13C_DIC的影响有限; 与Sr2+/Ca2+值一样, δ13C_DIC主要受径流条件控制, 其大小可以反映地下水径流条件的强弱.利用化学计量关系计算出由硫酸溶蚀碳酸盐岩的平均比例为22.64%, 产生的DIC(HCO₃-_H2SO4)占总DIC的平均比例为13.04%, 碳酸产生的DIC(HCO₃-_H2CO3)占地下水总DIC的比例为86.96%, 其中来源于土壤大气中的HCO₃-比例为43.48%.因此, 扣除硫酸对地下水中DIC的贡献后, 岩溶碳汇效应将减少13.04%.      

The contribution of agricultural and urban activities to inorganic carbon fluxes within temperate watersheds

The lateral transport of bicarbonate as dissolved inorganic carbon (DIC) to the oceans is an integral component of the global carbon budget and can represent the sequestration of CO₂ from the atmosphere. Recently studies have implicated land use change, in particular agricultural development, as an accelerator of bicarbonate export. However, due to the co-variation of land use, bedrock and surficial geologies, and the relationship between bicarbonate export and climate, the impact of anthropogenic activities on DIC export remains an important research question. In order to examine the land use controls on DIC export from small temperate watersheds we sampled 19 streams draining catchments of varying land uses with similar bedrock and surficial geologies. In addition to an agricultural effect, there was a strong correlation between the percent of watershed in urban development and DIC concentrations and DIC yields. Urban watersheds exported 7.8 times more DIC than their nearby forested counterparts and 2.0 times more DIC than nearby agricultural catchments. Isotopic data suggest that excess DIC export from altered systems results from increased chemical weathering, enhanced CO₂ production within urban green spaces, and as a result of organic matter loading from septic systems and leaky sewer lines. Furthermore, we found that nitrogen additions (e.g. fertilizers and manure) are aiding in the dissolution of lime, increasing the total export of DIC from agricultural watersheds. Calculated anthropogenic loading rates ranged from 0.43 to 0.86 mol C m^− 2 yr^− 1. These loading rates suggest that a significant portion of global DIC export might be attributable to human activities, although the impacts on CO₂ sequestration are difficult to determine.     

Effects of land use and cultivation time on soil organic and inorganic carbon storage in deep soils

The vertical distribution and exchange mechanisms of soil organic and inorganic carbon(SOC, SIC) play an important role in assessing carbon(C) cycling and budgets. However, the impact of land use through time for deep soil C(below 100 cm) is not well known. To investigate deep C storage under different land uses and evaluate how it changes with time, we collected soil samples to a depth of 500 cm in a soil profile in the Gutun watershed on the Chinese Loess Plateau(CLP); and determined SOC, SIC, and bulk density. The magnitude of SOC stocks in the 0–500 cm depth range fell into the following ranking: shrubland(17.2 kg m~(-2)) grassland(16.3 kg m~(-2)) forestland(15.2 kg m~(-2)) cropland(14.1 kg m~(-2)) gully land(6.4 kg m~(-2)). The ranking for SIC stocks were: grassland(104.1 kg m~(-2)) forestland(96.2 kg m~(-2)) shrubland(90.6 kg m~(-2)) cropland(82.4 kg m~(-2)) gully land(50.3 kg m~(-2)). Respective SOC and SIC stocks were at least 1.6-and 2.1-fold higher within the 100–500 cm depth range, as compared to the 0–100 cm depth range. Overall SOC and SIC stocks decreased significantly from the 5 th to the 15 th year of cultivation in croplands, and generally increased up to the 70 th year. Both SOC and SIC stocks showed a turning point at 15 years cultivation, which should be considered when evaluating soil C sequestration. Estimates of C stocks greatly depends on soil sampling depth, and understanding the influences of land use and time will improve soil productivity and conservation in regions with deep soils.