布达佩斯国际地球化学会议

1959年10月5-10日在布达佩斯举行了国际地球化学会議,这次会議是由匈牙利人民共和国科学院地质委員会召开的。参加会議的有11个国家的学者。会议研究了与岩浆岩的成因及矿化現象有关的地球化学问题。此外还討論了有关岩浆岩分类学及其统一名称的问题。专門的地球化学方法和某些一般性的及理论性的地球化学問題,也得到很大的注意。为了查明匈牙利第三紀火山作用和匈牙利某些类型的矿床的特点,曾經瑪特拉、托卡依和别尔任山区,以及鋁土矿区作了为期三天购旅行。     

数学方法在矿产地质工作中的应用

随着数学地质的发展,数学方法和电子计算机在矿产地质工作中的应用日益广泛和深入,不断解决愈来愈多的矿产地质实践问题和理论问题。这种应用大体上可归纳为以下三个方面(1)数学方法和电子计算机应用于矿产地质工作的每一个阶段。由矿产的普查勘探、详查评价、储量计算直至矿产开发,每一个阶段的矿产地质问题都能用数学方法和电子计算机帮助解决,以提高每一个阶段中矿产地质工作的速度和质量。     

用最优分割法处理华北地区前寒武纪变质岩系的同位素年龄数据

前言随着地质工作的不断发展,进一步利用同位素地质年龄资料研究和解决地质问题显得越来越重要。我国同位素地质年代学的研究在迅速的发展过程中积累了大量资料。如何根据数学原理,用电子计算机处理和利用这些资料是当前急待解决的问题。本文企图在这方面做些尝试,探索处理和利用同位素地质年龄资料的新方法。     

数学方法在地层和地质构造研究中的某些应用

解放后,在中国共产党和毛主席的英明领导下,全国地质研究工作迅速开展。在全国进行了大量的地质勘探和地质研究工作,累积了十分丰富地质资料和分析数据。生产实践要求应用数学方法对地质资料进行整理、解释和模拟,定量地描述地质体空间和时间变化,阐明在复杂条件下各种因素的影响,以便从已有的数据中能取得更多的信息,更好地探索内在规律性。随着国内自制电子计算机的应用与普及,提供了完成上述任务的必要条件。本文仅将几年来我们进行研究的某些成果简要介绍一下。关于所用方法的详细介绍参阅有关文献。     

展望矿物学今后的发展方向

地质科学的研究任务基本上有两大内容:一是追溯地质现象的发展历史,一是推论地表以下的地质情况。两者都是要寻求和阐明地质体(岩石、矿物、矿石、古生物、地下水等)在时间和空间上的质和量的变化。而所有地质现象演变的基本原因是物质的能量的变化。地壳运动,岩浆和变质作用,风化和沉积现象,成矿作用等,无一不是由于能量变化所致。变化的结果就使物质的总能量达到与周围环境相适应的程度,即暂时的平衡状态。     

受断裂面性质控制的构造位移场的数学模拟

地质体有着十分复杂的结构和构造,因此,如何掌握地质体中各点的位移规律和应力分布规律,对工程地质研究,预测矿山边坡稳定性和地下工程稳定性,地震预测和预报以及地质构造形变的规律都是十分重要的。     

扬子古板块的形成及其对中国南方地壳发展的影响

六十年代以来,人们在海洋和大陆边缘积累了大量地质、地球物理和地球化学资料,应运而生的“板块学说”,把人们的视野扩展到占地球表面百分之七十的广阔海域,使人们看到了有关洋壳演变为陆壳的许多独特的地质现象,使原来主要在大陆上获得认识的一些地质现象要求新的解释。本文将在前人地质资料基础上,利用板块学说探讨扬子古板块的形成和对中国南方地壳发展的影响。     

深切缅怀老一代地质学家李捷

李捷,字月三,1894年4月29日生于河北成安县西野庄。1913年保定育英中学毕业后考入工商部地质研究班(后改名“农商部地质研究所”),就学于章鸿钊、丁文江、翁文灏等一代宗师,是中国自己培养的第一批地质工作者。1916年秋,该班有18人拿到毕业文凭(史称“十八罗汉”,其中有李捷),全都进入农商部地质研究所任调查员,曾在我国的区域地质填图和矿产调查方面做了大量开创性、奠基性的工作。     

“板内形变与晚期成藏”出版

为纪念孙肇才先生从事石油地质工作50周年,以“板内形变与晚期成藏”为书名的孙肇才石油地质论文集2003年由地质出版社出版。全书精选了孙先生的论著24篇,分“基础地质”(3篇)、“中国含油气盆地综述”(3篇)、“典型含油气盆地分析”(10篇)和“在中外咨询会议上的发言”(8篇)4部分。书末附有孙先生学术论著和报告目录。全书共332页,约53万字。书中论述了中国含油气盆地的构造格局、成因机制、石油地质特征和油气远景。     

论岩体力学模型

岩体力学是研究现状的地质体受力条件改变时产生变形、破坏及其力学性质形成规律的科学。地质体与一般材料不同,由于其成因和经历的历史过程不同,致使其成分、结构及其形成条件不同。故现状的地质体当受力条件改变时,其力学作用,即变形和破坏机理亦不同。在进行岩体力学研究时,必须清楚地看到这一点。当前岩体力学研究成效不大的重要原因之一,就是没有注意地质体这一特点,在进行岩体力学研究时,不加分析地把地质体一律做为连续介质力学模型处理,显然是不合适的。     

Sedimentology and isotope geochemistry of lacustrine carbonates of the Oligocene Campins Basin, north-east Spain

The non-marine Campins Basin developed in the Oligocene, during a period of early rifting of the Catalan Coastal Ranges. Lacustrine deposits, interbedded between two alluvial units, comprise shallow and deep lacustrine facies. The lower, shallow lacustrine facies are made up of microbialite buildups and thin limestone beds. In the studied area, these facies are overlain by deep lacustrine facies which consist of alternations of several, metre-thick carbonate- and mudstone-dominated intervals. In addition to calcite, which is characteristic of the shallow lacustrine facies, aragonite and abundant dolomite are present in the deep lacustrine facies. This mineralogical change in the sequence reflects an overall increase in the Mg/Ca ratio of the lake waters. The deep lacustrine sequences are interpreted as having formed in a hydrologically closed basin that was subject to changes in the Mg/Ca ratio of the water, probably related to variations in the evaporation/precipitation rate. The sedimentological, mineralogical and isotopic characteristics of the Campins Basin dolomites suggest that, in general, they are primary in origin. The stable isotope data show an approximate covariance between δ¹³C and δ¹⁸O in the lower shallow lacustrine carbonates (calcite) which suggests that they formed during the onset of closure of the lake. The δ¹³C and δ¹⁸O values of the deep lacustrine carbonates display three different clusters that are roughly related to the carbonate mineralogy. Normalisation with respect to calcite of the isotopic compositions of dolomite and aragonite from the deep lacustrine carbonates allows the integration of all these isotope values into one covariant trend. The sequential appearance of different carbonate minerals and the isotopic covariant trend may indicate an overall evaporative concentration of the lake waters. The change in slope of the covariant trend for the isotope values between the shallow and the deep lacustrine carbonates might reflect the change in the waterbody morphology recorded in the basin fill sequence.     

A study of oxygen isotopic fractionation during bio-induced calcite precipitation in eutrophic Baldeggersee,Switzerland

In order to better understand environmental factors controlling oxygen isotope shifts in autochthonous lacustrine carbonate sequences, we undertook an extensive one-year study (March, 1995 to February, 1996) of water-column chemistry and daily sediment trap material from a small lake in Central Switzerland. Comparisons between calculated equilibrium isotope values, using the fractionation equation of Friedman and O’Neil, (1977) and measured oxygen isotope ratios of calcite in the sediment-traps reveal that oxygen isotopic values of autochthonous calcite (δ¹⁸O) are in isotopic equilibrium with ambient water during most of the spring and summer, when the majority of the calcite precipitates. In contrast, small amounts of calcite precipitated in early-spring and again in late-autumn are isotopically depleted in ¹⁸O relative to the calculated equilibrium values, by as much as 0.8‰. This seasonally occurring apparent isotopic nonequilibrium is associated with times of high phosphorous concentrations, elevated pH (∼8.6) and increased [CO₃²⁻] (∼50 μmol/l) in the surface waters. The resulting weighted average δ¹⁸O value for the studied period is −9.6‰, compared with a calculated equilibrium δ¹⁸O value of −9.4‰. These data convincingly demonstrate that δ¹⁸O of calcite are, for the most part, a very reliable proxy for temperature and δ¹⁸O of the water.     

Carbon and Oxygen Isotopic Composition of Surface‐Sediment Carbonate in Bosten Lake (Xinjiang,China) and its Controlling Factors

Bosten Lake is a mid-latitude lake with water mainly supplied by melting ice and snow in the Tianshan Mountains. The depositional environment of the lake is spatially not uniform due to the proximity of the major inlet and the single outlet in the western part of the lake. The analytical results show that the carbon and oxygen isotopic composition of recent lake sediments is related to this specific lacustrine depositional environment and to the resulting carbonate mineralogy. In the southwestern lake region between the Kaidu River inlet and the Kongqi River outlet, carbon isotope composition (δ13C) values of the carbonate sediment (?1‰ to ?2‰) have no relation to the oxygen isotope composition of the carbonate (δ18O) values (?7‰ to ?8‰), with both isotopes showing a low variability. The carbonate content is low (<20%). Carbonate minerals analyzed by X-ray diffraction are mainly composed of calcite, while aragonite was not recorded. The salinity of the lake water is low in the estuary region as a result of the Kaidu River inflow. In comparison, the carbon and oxygen isotope values are higher in the middle and eastern parts of the lake, with δ13C values between approximately +0.5‰ and +3‰, and δ18O values between ?1‰ and ?5‰. There is a moderate correlation between the stable oxygen and carbon isotopes, with a coefficient of correlation r of approximately 0.63. This implies that the lake water has a relatively short residence time. Carbonate minerals constitute calcite and aragonite in the middle and eastern region of the lake. Aragonite and Mg–calcite are formed at higher lake water salinity and temperatures, and larger evaporation effects. More saline lake water in the middle and eastern region of the lake and the enhanced isotopic equilibrium between water and atmospheric CO2 cause the correlating carbon and oxygen isotope values determined for aragonite and Mg–calcite. Evaporation and biological processes are the main reasons for the salinity and carbonate mineralogy influence of the surface-sediment carbonate in Bosten Lake. The lake water residence time and the CO2 exchange between the atmosphere and the water body control the carbon and oxygen isotope composition of the carbonate sediment. In addition, organic matter pollution and decomposition result in the abnormally low carbon isotope values of the lake surface-sediment carbonate.     

Changes to depositional palaeoenvironments within the Qikou depression (Bohaiwan Basin,China): carbon and oxygen isotopes in lacustrine carbonates of the Palaeogene Shahejie Formation

This paper reports the carbon and oxygen isotope compositions of lacustrine carbonate sediments from the Palaeogene Shahejie Formation, Qikou depression, Bohaiwan Basin, with the aim of determining the palaeoenvironmental conditions in the region. Results from Es₂, the second member of the Shahejie Formation, showed values of δ¹³C and δ¹⁸O from –1.2‰ to +2.4‰ (average +0.6‰) and from –6.8‰ to –4.7‰ (average –5.7‰), respectively, suggesting a relatively hot climate attending deposition. The slightly closed nature of the lake, which contains brackish water, resulted in higher carbonate δ¹³C and δ¹⁸O values than in a meteoric environment. The values of δ¹³C and δ¹⁸O preserved within the carbonates of the overlying lower Shahejie I (Es₁) varied between +1.3‰ and +4.9‰ (average +3.2‰) and from ?4.4‰ to ?1.8‰ (average ?3.1‰), respectively, indicating that the climate became colder at that time. Subsequently, a marine transgression caused the salinity of the lake water to increase. The values of δ¹³C and δ¹⁸O were controlled by salinity. The high δ¹³C values were also influenced by the rapid burial of the lake organisms and by algal photosynthesis. Values of δ¹³C and δ¹⁸O from carbonates in upper Es₁ ranged from ?8.0‰ to +11.0‰ (average +10.1‰) and from ?5.0‰ to ?1.5‰ (average ?3.4‰), respectively, indicating a slight increase in the temperature over time. In the closed and reducing environment, extremes in δ¹³C values resulted from biochemical fermentation. The positive δ¹³C excursion recorded in the carbonates of the Shahejie Formation in the Qikou depression indicates that the palaeoclimate underwent a significant transformation during the Eocene and the Oligocene.     

Contrasting Carbon and Oxygen Isotopic Evolution in Metacarbonates from the Kerala Khondalite Belt,Southern India

The Kerala Khondalite belt is a Proterozoic metasupracrustal granulite facies terrain in southern India comprising garnet-biotite gneiss, garnet-sillimanite gneiss and orthopyroxene granulites as major rock types. Calc-silicate rocks and marbles, occurring as minor lithologies in the Kerala Khondalite Belt, show different mineral assemblages and reaction histories of which indicate a metamorphic P-T-fluid history dominated by internal fluid buffering during the peak metamorphism, followed by external fluid influx during decompression. The carbon and oxygen isotopic compositions of calcite from three representative metacarbonate localities show contrasting evolutionary trends. The Ambasamudram marbles exhibit carbon and oxygen isotope ratios (δ¹³C ∼ 0‰ and δ¹⁸O ∼ 20‰) typical of middle to late Proterozoic marine carbonate sediments with minor variation ascribed to the isotopic exchange due to the devolatilization reactions. The δ¹³C and δ¹⁸O values of ∼ −9‰ and 11‰, respectively, for calcite from calc-silicate rocks at Nuliyam are considerably low and heterogeneous. The wollastonite formation here, possibly corresponds to an earlier event of fluid infiltration during prograde to peak metamorphism, which resulted in decarbonation and isotope resetting. Further, petrologic evidence supports a model of late carbonic fluid infiltration that has partially affected the calc-silicate rocks, with subsequent isotope resetting, more towards the contact between calc-silicate rock and charnockite. At Korani, only oxygen isotopes have been significantly lowered (δ¹⁸O ∼ 13‰) and the process involved might be a combination of metamorphic devolatilization accompanied by an aqueous fluid influx, supported by petrologic evidence. The stable isotope signatures obtained from the individual localities, thus indicate heterogeneous patterns of fluid evolution history within the same crustal segment.     

Depositional environments and diagenesis in Lake Parakeelya: a Cambrian alkaline playa from the Officer Basin, South Australia

Laminated and desiccated siliceous dolostones, dolomitic mudstones and dolomitic sandstones in the Cambrian Parakeelya Alkali Member of the Observatory Hill Formation accumulated in an alkaline playa. Four facies are recognized (from lake centre to lake edge): lake, saline mudflat, dry mudflat and sandflat facies. The facies occur in cycles. Cycles of tens of metres thickness record the gradual expansion and contraction of the playa. Superimposed smaller cycles of tens of centimetres thickness record minor oscillations in the position of the strandline in a shallow lake. The dominance of saline mudflat, dry mudflat and sandflat facies indicates that the lake was rimmed by broad flat areas with negligible relief. The high δ¹⁸O values of primary and penecontemporaneous diagenetic carbonates of +24 to +28‰ (SMOW) indicate strong evaporation of ground and surface waters within the lake system. Calcite pseudomorphs of the sodium carbonate minerals trona and shortite have δ¹⁸O values between + 19 and + 22.5‰, and contain fluid inclusions with variable salinites and homogenization temperatures up to around 110°C. This suggests that the euhedral alkaline evaporites were dissolved by heated waters; calcite pseudomorphs then precipitated from a mixed solution formed by the interaction of these incoming fluids with the relatively saline interstitial brines. The sodium bicarbonate solutions formed by dissolution of the evaporites would have been dispersed by the basinal brines so that despite the closed drainage, further groundwater concentration did not take place.     

Sedimentological and palaeohydrological responses to tectonics and climate in a small, closed, lacustrine system: Oligocene As Pontes Basin (Spain)

ABSTRACT A small, closed, lacustrine system developed during the restraining overstep stages of the Oligocene As Pontes strike‐slip basin (Spain). The increase in basin accommodation and the headward spread of the drainage, which increased the water input, triggered a change from shallow, holomictic to deeper, meromictic conditions. The lower, shallow, lacustrine assemblage consists of mudstone–carbonate cycles recording lacustrine–palustrine ramp deposition in a saline lake. High Sr content in some early diagenetic calcites suggests that aragonite and calcite made up the primary carbonate muds. Early dolomitization took place together with widespread pedogenic activity. The upper, deep, freshwater, lacustrine assemblage includes bundles of carbonate–clay rhythmites and fine‐grained turbidite beds. Primary calcite and diagenetic siderite make up the carbonate laminae. The Mg content of the primary carbonates records variations in Mg/Ca ratios in lacustrine waters. δ¹⁸O and δ¹³C covariance trends in calcite reinforce closed drainage conditions. δ¹⁸O data indicate that the lake system changed rapidly from short‐lived isotopically light periods (i.e. from seasonal to pluriannual) to longer steady‐state periods of heavier δ¹⁸O (i.e. from pluriannual to millennial). The small δ¹³C changes in the covariant trends were caused by dilute inflow, changing the contributions of dissolved organic carbon in the system and/or internal variations in lacustrine organic productivity and recycling. In both shallow and deep carbonate facies, sulphate reduction and methanogenesis may account, respectively, for the larger negative and positive δ¹³C shifts recorded in the early diagenetic carbonates (calcite, dolomite and siderite). The lacustrine system was very susceptible to high‐frequency, climatically forced water balance variations. These climatic oscillations interfered with the low‐frequency tectonic and morphological changes in the basin catchment. This resulted in the superposition of high‐order depositional, mineralogical and geochemical cycles and rhythms on the lower order lacustrine infill sequence.     

Palaeoenvironmental reconstruction of a middle Miocene alluvial fan to cyclic shallow lacustrine depositional system in the Calatayud Basin (NE Spain)

ABSTRACT The middle Miocene sedimentary fill of the Calatayud Basin in north‐eastern Spain consists of proximal to distal alluvial fan‐floodplain and shallow lacustrine deposits. Four main facies groups characteristic of different sedimentary environments are recognized: (1) proximal and medial alluvial fan facies that comprise clast‐supported gravel and subordinate sandstone and mudstone, the latter exhibiting incipient pedogenic features; (2) distal alluvial fan facies, formed mainly of massive mudstone, carbonate‐rich palaeosols and local carbonate pond deposits; (3) lake margin facies, which show two distinct lithofacies associations depending on their distribution relative to the alluvial fan system, i.e. front (lithofacies A), comprising massive siliciclastic mudstone and tabular carbonates, or lateral (lithofacies B) showing laminated and/or massive siliciclastic mudstone alternating with tabular and/or laminated carbonate beds; and (4) mudflat–shallow lake facies showing a remarkable cyclical alternation of green‐grey and/or red siliciclastic mudstone units and white dolomitic carbonate beds. The cyclic mudflat–shallow lake succession, as exposed in the Orera composite section (OCS), is dominantly composed of small‐scale mudstone–carbonate/dolomite cycles. The mudstone intervals of the sedimentary cycles are interpreted as a result of sedimentation from suspension by distal sheet floods, the deposits evolving either under subaerial exposure or water‐saturated conditions, depending on their location on the lacustrine mudflat and on climate. The dolomite intervals accumulated during lake‐level highstands with Mg‐rich waters becoming increasingly concentrated. Lowstand to highstand lake‐level changes indicated by the mudstone/dolomite units of the small‐scale cycles reflect a climate control (from dry to wet conditions) on the sedimentation in the area. The spatial distribution of the different lithofacies implies that deposition of the small‐scale cycles took place in a low‐gradient, shallow lake basin located in an interfan zone. The development of the basin was constrained by gradual alluvial fan aggradation. Additional support for the palaeoenvironmental interpretation is derived from the isotopic compositions of carbonates from the various lithofacies that show a wide range of δ¹⁸O and δ¹³C values varying from ?7·9 to 3·0‰ PDB and from ?9·2 to ?1·7‰ PDB respectively. More negative δ¹⁸O and δ¹³C values are from carbonate‐rich palaeosols and lake‐margin carbonates, which extended in front of the alluvial fan systems, whereas more positive values correspond to dolomite beds deposited in the shallow lacustrine environment. The results show a clear trend of δ¹⁸O enrichment in the carbonates from lake margin to the centre of the shallow lake basin, thereby also demonstrating that the lake evolved under hydrologically closed conditions.     

Carbon and Oxygen Isotopic Compositions: How Lacustrine Environmental Factors Respond in Northwestern and Northeastern China

Surface lake sediments,28 from Hoh Xil,24 from northeastern China,99 from Lake Bosten,31 from Ulungur and 26 from Heihai were collected to determine δ13C and δ18O values.Considering the impact factors,conductivity,alkalinity,pH,TOC,C/N and carbonate-content in the sediments,Cl,P,S,and metal element ratios of Mg/Ca,Sr/Ca,Fe/Mn of bulk sediments as environmental variables enable evaluation of their influences on δ13C and δ18O using principal component analysis(PCA) method.The closure and residence time of lakes can influence the correlation between δ13C and δ18O.Lake water will change from fresh to brackish with increasing reduction and eutrophication effects.Mg/Ca in the bulk sediment indicates the characteristic of residence time,Sr/Ca and Fe/Mn infer the salinity of lakes.Carbonate formation processes and types can influence the δ13C–δ18O correlation.δ18O will be heavier from Mg-calcite and aragonite formed in a high-salinity water body than calcite formed in freshwater conditions.When carbonate content is less than 30%,there is no relationship with either δ13C or δ18O,and also none between δ13C and δ18O.More than 30%,carbonate content,however,co-varies highly to δ13C and δ18O,and there is also a high correlation between δ13C and δ18O.Vegetation conditions and primary productivity of lakes can influence the characteristics of δ13C and δ18O,and their co-variance.Total organic matter content(TOC) in the sediments is higher with more terrestrial and submerged plants infilling.In northeastern and northwestern China,when organic matter in the lake sediments comes from endogenous floating organisms and algae,the δ13C value is high.δ13C is in the range of 4‰ to 0‰ when organic matter comes mainly from floating organisms(C/N<6);in the range of 4‰ to 8‰ when organic matter comes from diatoms(C/N=6 to 8);and 8‰ to 4‰ when organic matter comes from aquatic and terrestrial plants(C/N>8).     

Fibrous calcite from the Ordovician of Tennessee: preservation of marine oxygen isotopic composition and its implications

Three categories of fibrous calcite from early to middle Caradoc platform-marginal buildups in east Tennessee can be delineated using cathodoluminescent microscopy, minor element chemistry and stable C-O isotopic composition. Bright luminescent fibrous cement has elevated Mn (>1000 p.p.m.), negative δ¹³C and intermediate δ¹⁸O values relative to other types of fibrous calcite. This cement reflects fibrous calcite that interacted with reducing Mn-rich fluids. Dully luminescent fibrous cement has elevated Fe (>400 p.p.m.), positive δ¹³C and negative δ¹⁸O values relative to other fibrous cements. This cement was stabilized by burial fluids. Nonluminescent fibrous cement has low Mn and Fe (generally below 400 p.p.m.) and positive δ¹³C and δ¹⁸O values relative to other types of fibrous calcite. The latter cement is interpreted to be the best material for determining the isotopic composition of calcite precipitated in equilibrium with early to middle Caradoc seawater, which is δ¹³C=1% PDB and δ¹⁸O=?4 to ?5‰ PDB. Results from this study and Ashgillian brachiopods indicate that the average δ¹⁸O composition of the Ordovician ocean, during nonglacial periods, was probably never more negative than ?3‰ SMOW. Assuming an Ordovician seawater δ¹⁸O value of ?1‰ SMOW, Holston Formation fibrous cements would have precipitated at temperatures between 27 and 36 °C, which is near the upper temperature limit for metazoans. A seawater δ¹⁸O value of ?2‰ SMOW yields temperatures ranging from 23 to 31 °C, while a ?3‰ SMOW value yields temperatures of 18–26 °C.