Identification and occurrence of novel C36–C54 3,4-dialkylthiophenes with an unusual carbon skeleton in immature sediments

A series of novel long-chain 3,4-dialkylthiophenes (C₃₆–C₅₄) was identified in a number of sediments ranging from Pleistocene to Cretaceous. The identifications were based on mass spectral characterisation, desulphurisation and mass spectral data of synthesised model compounds. These organic sulphur compounds are probably formed by sulphur incorporation into mid-chain dimethylalkadienes with two methylenic double bonds. These putative precursor lipids are unprecedented and may be considered rather unusual. The distribution of 3,4-dialkylthiophenes in sediments varies considerably with the depositional palaeoenvironment, indicating that these compounds have a potential as molecular markers reflecting changes in palaeoenvironment.     

Interaction between lateral sorting in river bends and vertical sorting in dunes

Sediment is sorted in river bends under the influence of gravity that pulls the heavier grains downslope and secondary flow that drags the finer grains upslope. Furthermore, when dunes are present, sediment is also sorted vertically at the dune lee side. However, sorting functions are poorly defined, since the relation to transverse bed slope and the interaction between lateral and vertical sorting is not yet understood for lack of data under controlled conditions. The objective of this study is to describe lateral sorting as a function of transverse bed slope and to gain an understanding of the interaction between lateral and vertical sorting in river bends. To this end, experiments were conducted with a poorly sorted sediment mixture in a rotating annular flume in which secondary flow intensity can be controlled separately from the main flow velocity, and therefore transverse bed slope towards the inner bend and dune dimensions can be systematically varied. Sediment samples were taken along cross-sections at the surface of dune troughs and dune crests, and over the entire depth at the location of dune crests (bulk samples), which enabled comparison of the relative contribution of vertical sorting by dunes to lateral sorting by the transverse bed slope. The data show that lateral sorting is always the dominant sorting mechanism in bends, and bulk samples showed minor effects of vertical sorting by dunes as long as all grain-size fractions are mobile. An empirical bend sorting model was fitted that redistributes the available sediment fractions over the cross-section as a function of transverse bed slope. Comparison with field data showed that the model accurately reproduces spatially-averaged trends in sorting at the bend apex in single-thread channels. The bend sorting model therefore provides a better definition of bend sorting with conservation of mass by size fraction and adds to current understanding of bend sorting. The implication for numerical modelling is that bend sorting mechanisms can be modelled independently of dunes, allowing the application of the active layer concept.     

Experimental studies of oxygen isotope fractionation in the carbonic acid system at 15°, 25°, and 40°C

In light of recent studies that show oxygen isotope fractionation in carbonate minerals to be a function of HCO₃⁻ and CO₃²⁻ concentrations, the oxygen isotope fractionation and exchange between water and components of the carbonic acid system (HCO₃⁻, CO₃²⁻, and CO_2(aq)) were investigated at 15°, 25°, and 40°C. To investigate oxygen isotope exchange between HCO₃⁻, CO₃²⁻, and H₂O, NaHCO₃ solutions were prepared and the pH was adjusted over a range of 2 to 12 by the addition of small amounts of HCl or NaOH. After thermal, chemical, and isotopic equilibrium was attained, BaCl₂ was added to the NaHCO₃ solutions. This resulted in immediate BaCO₃ precipitation; thus, recording the isotopic composition of the dissolved inorganic carbon (DIC). Data from experiments at 15°, 25°, and 40°C (1 atm) show that the oxygen isotope fractionation between HCO₃⁻ and H₂O as a function of temperature is governed by the equation:

     

青藏高原兹格塘错沉积记录的全新世水位变化事件及其原因初步研究

兹格塘错是一个内陆封闭型湖泊,位于藏北高原腹地,处于西南季风作用边缘地带。由于流域内无冰川分布,湖泊补给主要靠大气降水,因此水体的扩张与收缩能够直接反映西南季风的变化。半干旱气候地区湖泊沉积物碳酸盐含量能够敏感地反映水体的扩张与收缩。兹格塘错沉积物碳酸盐含量高,与可溶盐(氯离子与硫酸根离子)含量变化结合能更好地揭示水体的演化阶段。分析结果表明,在9.3～8.9calkaBP、8.3～7.8calkaBP、5.0～4.7calkaBP、4.0～3.8calkaBP和3.1～2.7calkaBP碳酸盐含量出现大幅度下降,指示湖泊淡化、水位升高。但在3.8calkaBP左右碳酸盐含量和可溶盐(氯离子与硫酸根离子)含量同时出现峰值,指示出湖泊水体盐度升高、水位出现下降;近1calkaBP以来,碳酸盐与可溶盐含量都呈现逐渐下降趋势,表明湖泊水体逐渐淡化、水位缓慢上升的过程。但近100a来可溶盐含量上升,指示出湖泊水体的不断浓缩和水位下降过程,这和近百年的气候暖干化过程是一致的。兹格塘错沉积岩心碳酸盐含量全新世以来5次极低事件,有力地证明青藏高原西南季风在全新世期间的不稳定性。     

Der geologische Bau und die tektonische Bedeutung der Balearischen Inseln

Ohne ZusammenfassungVortrag auf der Hauptversammlung in Frankfurt a. M. am 8. Jan. 1927.     

Interpretation of aeromagnetic data across the central crystalline shield area of Nigeria

Summary. A residual map of the total magnetic field (above 25 000 nT base) is presented for a portion of the central crystalline shield area of Nigeria and overlapping small portions of the Chad basin and the Benue rift (8°30'−12° 00'lat, and 7°−10°30' long). The map (based on a dataset digitized from recently released aeromagnetic sheets of Nigeria) leads to four results. (1) A magnetic boundary, evident on the map, separates the Younger Granite complexes into two groups. The groups are petrologically different, and the boundary may be a fault line with uplift to the south. (2) South of the boundary the map is dominated by a system of sub-parallel anomalies striking NE–SW, possibly representing major tectonic trends, and a set of fractures through which the Younger Granite complexes were intruded. The trend of the system parallels the Benue rift and lineaments in the oceanic crust off West Africa. (3) Negative magnetic anomalies lie over most of the known ring complexes, and over some suspected buried ring complexes and other intrusions. (4) 2½-and 3-D modelling shows that the larger complexes extend to 12 km depth, and the smaller ones to 6 km. They have nearly vertical sides, and magnetization contrasts range from 0.3 to 0.5 A m⁻¹.     

Analysis of some aromatic hydrocarbons in a benzene-soluble bitumen from Green River shale

The hydrocarbon content of an aromatic fraction, isolated from the bitumen of Green River shale, was studied by mass spectrometry, infra-red spectrometry, gas chromatography and a dehydrogenation technique. The hydrocarbon types and their distribution in this aromatic fraction, as determined by mass spectrometry, include the following: C_nH_2n?6(10%), C_nH_{2n?8 (31 %)}, C_nH_2n?10(18%), C_nH_2n?12(12%), C_nH_2n?14(8%) and a series of alkenylbenzenes (20%). The carbon-number range, empirical formulae and quantity of each compound in the major types are reported. Mass spectra of several compounds and homologous mixtures of compounds isolated from the aromatic fraction are also given.     

Transformations of the stuffed cristobalites, K2MSiO4, M=Mg, Zn, Co, Cd, with temperature and composition

The effects of composition and of temperature on the orthorhombic, Pca2 ₁ to cubic, F4ˉ3m transition of the stuffed cristobalite structure are reported. A distorton index which measures the departure of the orthorhombic unit cell from a metrically cubic cell shows that at room temperature, distortion increases in the progression K₂CdSiO₄ <K₂MgSiO₄ <K₂ZnSiO₄≈K₂CoSiO₄. High temperature X-ray powder measurements document an apparently discontinuous transition to a structure of F4ˉ3m symmetry. Differential scanning calorimetry shows a sharp, reversible, first order transition to the high temperature phase at about 500–600 °C for these compounds. Measured transformation enthalpies in the range of 7 to 16 J/g correlate roughly with the distortion index. The transformation involves tetrahedral rotation to an orientationally disordered cubic structure which retains an ordered M²⁺/Si distribution. Received: 8 November 1996 / Revised, accepted: 14 October 1997     

Geomorphological hazards related to deep dissolution phenomena in the Western Italian Alps: Distribution, assessment and interaction with human activities

Deep dissolution affects great part of soluble rocks (e.g. gypsum and anhydrite) of the Western Italian Alps. The related superficial phenomena (sinkholes, gravity-induced processes and a local worsening of geomechanical rock properties) are not limited to typical karsts landscape and cause slope instability also affecting populated sites and infrastructures. The paper aims to describe general characteristic of dissolution phenomena, to interpret their conditioning factors and evolutionary stages and to assess possible hazards due to their superficial effects.The search for evidences of deep dissolution leads to the selection of representative sites in the central part of the Western Italian Alps (Piemonte and Valle d'Aosta Region). Detailed geological and geomorphological studies have been used to classify the selected sites by type, size and variable state of activity. Very different evolutionary stages of dissolution phenomena have been interpreted by comparison of case-studies: some are early “embryonic”; others are more evolved, up to typical sinkholes, or even remodelled by other phenomena. Some cases show an extreme complexity in the interactions between corrosion phenomena and other geomorphic processes: slope deformations, from one side, and karst, fluvial and glacial phenomena, to the other. A wide range of movement rates on slope instabilities induced by deep dissolution have been estimated by topographic and geomorphic data. Geochemical data on removed rocks by dissolution indicate 0.4 mm/year values for local subsidence. Historical and technical data indicate low frequency of major dissolution-induced collapses, but highlight widespread damages to tunnels, roads and buildings, especially along slopes.