岩石变形所反映的地震作用过程--第13届国际变形机理、流变学和构造学学术会议概述

简要介绍了第13届国际变形机理、流变学和构造学学术会议的概况和特点，综述了地震变形作用的研究现状。     

Elucidation of the Alum Shale kerogen structure using a multi-disciplinary approach

The significance and validity of integrating data obtained from a variety of analytical techniques to understand, elucidate and model kerogen's complex chemical structure is reported here using degradative (open and closed system pyrolysis, chemical oxidation), non-degradative (¹³C CP/MAS NMR) and optical (incident white light and blue light) methods. Seven Cambrian Alum Shale samples, ranging in maturity from immature to post-mature with respect to petroleum generation, were studied and were chosen for their simple geological history, uniform organic matter type and high organic carbon content. The Alum Shale kerogens, which primarily consist of algal organic matter, liberate low molecular weight gaseous and aromatic compounds on pyrolysis and give mostly branched dicarboxylic acids on chemical oxidation. ¹³C NMR spectroscopy shows that the Alum Shale kerogens are anomalously rich in oxygen-bearing functional groups (such as C = O, ArCO, CHO, CH_xO), most of which apparently remain intact within the kerogen macro-molecule (KMM) through the diagenetic and catagenetic stages. Fragments released by different degradative techniques are quantified and the aromaticity (f_a), O/C and relative proportions of various carbon types estimated by ¹³C NMR. A synthesis of these data has allowed us to better understand the chemistry of the Alum Shale kerogen.     

Global synchroneity of a positive carbon isotope excursion at the Cenomanian/Turonian boundary: Validation by calcareous microfossil biostratigraphy of the Yezo Group, Hokkaido, Japan

Abstract Isotopic analyses of organic carbon from the mid-Cretaceous sequence in Hokkaido, Japan, revealed a 2‰ positive excursion of δ¹³C values at the biostratigraphically defined Cenomanian/Turonian (C/T) boundary recognized in the Yezo Group. The planktonic foraminiferal Whiteinella archaeocretacea Zone, which is known to bracket the Cenomanian/Turonian boundary elsewhere in the world, was recognized in the Oyubari area of central Hokkaido based on the distribution of commonly occurring planktonic foraminifera. In the Tappu area of northwestern Hokkaido, where diagnostic planktonic foraminifera are rare but calcareous nannoplankton occur commonly, the interval coeval with the W. archaeocretacea Zone can also be established by recognizing the conjoined last appearance levels of Corollithion kennedyi and Axopodorhabdus albianus, both calcareous nannoplankton species. Carbon isotope profiles exhibit a similar pattern with comparable peaks and troughs occurring in the same stratigraphic position in the sequences. A prominent, positive 2‰ shift of δ¹³C values, here called ‘δ¹³C spike’ occurs in the middle of the W. archaeocretacea Zone in the Oyubari area and just above the conjoined last appearances of the two above-mentioned nannoplankton taxa in the Tappu area. The Cenomanian/Turonian boundary can be drawn just above the peak position of the spike in both sections. The Rock Eval analyses and biomarker analyses of organic carbon indicate that organic carbon subjected to our isotope analyses is of terrestrial origin. Therefore, the observed 2%o shift should reflect changes in the isotopic composition of the atmospheric CO₂. A unique layer composed predominantly of sand-grain sized spumellarian Radiolaria is present immediately above the δ¹³C spike both in the Oyubari and Tappu areas, suggesting an increasing availability of both nutrients and silica in surface waters.     

西藏改则西北部喀湖错把拉湖区13kaBP以来的湖泊沉积与环境演化

通过对藏北喀湖错把拉湖区湖积剖面的研究,建立了该区13kaBP以来的沉积序列,并将13kaBP以来的气候划分为2个干冷期和2个湿润期。其中2个湿润期和第二旋回的干冷期可分别与北半球第一、二新高温期和第二新冰期大致对比,基本反映了末次冰消期以来全球气候变化的一般规律,青藏高原腹地对于全球气候变化的响应是比较敏锐的。     

Assessment of δ13C and C/N ratios in bulk organic matter as palaeosalinity indicators in Holocene and Lateglacial isolation basin sediments,northwest Scotland

Carbon isotopes (δ¹³C) and C/N ratios from bulk organic matter have recently been used as alternative proxies for relative sea‐level (RSL) reconstruction where there are problems associated with conventional biological indictors. A previous study on a single isolation basin (Upper Loch nan Eala) in northwest Scotland has shown a clear relationship between δ¹³C, C/N ratios and palaeosalinity from Younger Dryas and Holocene aged sediments. In this paper we present results of δ¹³C and C/N ratio analyses from other isolation basins in northwest Scotland over the Holocene and the Lateglacial period in order to validate this technique. The results from the Holocene sequences support the earlier findings that this technique can be used to identify RSL change from isolation basins over the Holocene in this region. The relationship between δ¹³C, C/N ratios and RSL change is not apparent in sediments of Lateglacial age. Other environmental variables such as atmospheric CO₂ concentration, poor vegetation development and temperature influence δ¹³C values during this period. Copyright © 2007 John Wiley & Sons, Ltd.     

Nature and role of CO2 in some hot and cold HCO3/Na/CO2-rich Portuguese mineral waters: a review and reinterpretation

 At the northern part of the Portuguese mainland, the upflow zone of several hot and cold HCO₃/Na/CO₂-rich mineral waters is mainly associated with important NNE–SSW faults. Several geochemical studies have been carried out on thermal and non-thermal hydromineral manifestations that occur along or near these long tectonic alignments. The slight chemical differences that exist between these meteoric hot and cold HCO₃/Na/CO₂-rich mineral waters seem to be mainly caused by CO₂. δ¹³C_(TIDC) values observed in these groundwaters range between –6.00 and –1.00‰ versus V-PDB (V denotes Vienna, the site of the International Atomic Energy Agency; PDB originates from the CaCO₃ of the rostrum of a Cretaceous belemnite, Belemnitella americana, collected in the Peedee formation of South Carolina, USA) indicating a deep-seated (mantle) origin for most of the CO₂. Nevertheless, in the case of the heavier δ¹³C_(TIDC) values, the contribution of metamorphic CO₂ or the dissolution of carbonate rock levels at depth cannot be excluded. Concerning the hot waters, the lack of a positive ¹⁸O-shift should be attributed to water-rock interaction in a low temperature environment, rather than to the isotopic influence of CO₂ on the δ¹⁸O-value of the waters. Received: 9 August 1999 · Accepted: 8 March 2000     

西北冰洋表-底层碳动力学耦合作用的同位素(13C,234Th)指示

The coupling of upper ocean-benthic carbon dynamics in the ice-free western Arctic Ocean(the Chukchi Sea and the Canada Basin) was evaluated during the late July–early September 2003 using natural stable(13C) and radioactive(238U-234Th) isotope tracers. POC export flux estimated from 234Th/238 U disequilibria and dissolved CO2 concentration([CO2(aq)]) pointed out that the strengthened biological pump in the Chukchi Shelf have significantly lowered [CO2(aq)] and altered the magnitude of isotopic(12C/13C) fractionation during carbon fixation in the surface ocean. Further, d13 C signatures of surface sediments(d13Csed) are positively correlated to those of weighted d13 CPOC in upper ocean(d13Csed =13.64+1.56×d13CPOC, r2=0.73, p0.01), suggesting that the POC isotopic signals from upper ocean have been recorded in the sediments, partly due to the rapid export of particles as evidenced by low residence times of the highly particle-reactive 234 Th from the upper water column. It is suggested that there probably exists an upper ocean-benthic coupling of carbon dynamics, which likely assures the sedimentary d13 C record an indicator of paleo-CO2 in the western Arctic Ocean.     

碳酸盐岩碳同位素地层学研究中数据的有效性

碳酸盐岩碳稳定同位素组成数据能否有效地反应原始大洋的同位素组成是稳定同位素地层学研究成败的关键,因此,如何准确地判断碳同位素比值的有效性成为该稳定同位素地层学研究中的焦点问题之一。碳同位素值有效性受成岩作用、地层缺失、样品处理过程等多方面因素影响,但成岩作用是诸多因素中最普遍、最主要的,因而正确判别碳同位素值可靠性通常也就是对样品及其同位素组成经受成岩改造程度的评定。确保碳同位素测试结果可靠应主要把握前期严格选样和后期数据分析两个重要环节。前期选样包括野外和室内两步,是在宏观尺度上对数据可靠性的把握;后期数据分析则主要是在严格选样的基础上,利用碳(及附带的氧)同位素自身数据特征以及借助Mn、Fe、Sr等微量元素特征从元素级别的微观角度对同位素值有效性做出进一步判别。     

13X分子筛活化及其对氧气转移时吸附/解吸过程中氧同位素分馏效应的研究

在激光BrF5法分析硅酸盐和氧化物矿物的真空提取流程中,通常采用氧气作为工作气体来测定样品的氧同位素组成。这需要使用分子筛吸附并转移氧气到质谱进样系统,而分子筛的活化对于有效吸附和解吸氧气至关重要,否则会引起分析过程中的氧同位素分馏。通过采用13X分子筛进行多组实验分析,笔者发现用不同活化程度或中毒失活分子筛沸石转移时可能存在氧同位素分馏。在低温下分子筛是不能够活化的(或活化不完全),吸附能力很低,所测定的δ18O值是波动的。在200℃马弗炉中预加热24h,然后迅速转移到温度为100℃、真空度为10-3Pa系统中加热12h的分子筛,对氧气吸附能力很强,氧同位素分析的绝对误差为±0.05‰(1σ),能够满足地球化学氧同位素分析的要求。如果分子筛受BrF5污染,其吸附能力大为降低,测定的δ18O值呈下降趋势,氧同位素分馏高达0.7‰。如果分子筛受水汽污染,质谱接受电压不断地降低,存在解吸温度下的再吸附过程,测定δ18O值呈上升趋势。因此,分子筛在使用前要在适当条件下的活化,在发现污染或测量值发生波动变化时要及时更换,否则难以保证氧同位素分析数据的可靠性。