Sequential extraction procedure in columns. Part 1: Development and description of a new method

A sequential extraction procedure was carried out in columns using reagents that are known to be reliable from batch tests. The intention was to distinguish between different chemical forms of iron and heavy metals in samples from reduced porous aquifers, which demands anaerobic conditions for the extraction procedure and the determination of small amounts of reactive mineral phases in a quartz dominated sediment system. By means of the developed method, anaerobic conditions can be guaranteed in the columns, which could not be realized to full satisfaction in batch tests that were carried out in a glove box. In order to distinguish between the fractions that were water soluble, exchangeable, bound to carbonates and bound to hydroxides, different reagents were pumped through the sediments and sampled after passage of the columns. Sediment samples of 10 kg each were investigated in this way. The extraction steps were known to be complete when analyses revealed that no further major and trace elements were leached out of the columns. This approach enabled well-adjusted amounts of reagents to be used. By means of the sequential extraction procedure in columns the composition of even small amounts of reactive mineral phases can be determined successfully, which contributes to a deeper understanding of the hydrogeochemical processes in aquifers. In batch tests this accuracy cannot be reached because of the surplus of the extraction solution in relation to the amount of sediment (higher solution-sediment ratio). Furthermore, larger samples are much more representative of the composition of the aquifers than smaller ones and the heterogeneity of the sediment does not limit the accuracy of the results as much as in batch tests. In addition, the technique of flushing sediment in a column is much more typical for the situation in an aquifer than suspending a few grams of a sample in the extracting reagents in batch extraction tests. In order to demonstrate the methodical improvements and field applications, the newly developed method was used to investigate the changing binding forms and mobility of iron and trace metals in samples from a lignite overburden dump, which are influenced by pyrite oxidation processes (acidification) followed by the addition of crushed limestone (neutralization) (see "Sequential extraction procedure in columns. Part 2: Application of a new method").     

青藏高原东缘晚新生代成都盆地物源分析与水系演化

成都盆地位于青藏高原东缘,夹于龙门山与龙泉山之间,盆地中充填了3.6Ma以来的大邑砾岩、雅安砾石层和晚更新世—全新世砾石层,其物源均来源于盆地西侧的龙门山,具横向水系和单向充填的特征。本次以物源区分析作为切入点,以岷江和青衣江水系为重点,采用砾岩成分分析、砂岩岩屑成分分析、重矿物分析和砾石的地球化学分析等基本方法,开展青藏高原东缘晚新生代以来的古水系重建工作,研究结果表明,成都盆地主要有两个物源区,其中成都盆地北部的都江堰街子场、崇州白塔山、大邑白岩沟、大邑氮肥厂、彭州丁家湾、彭州葛仙山等剖面中的砾石层在碎屑成分、重矿物和花岗岩砾石的地球化学成分等方面相似,应为古岷江的产物,而其与现代岷江在砾岩成分和重矿物特征等方面的差异性则表明古岷江可能存在改道的现象;成都盆地南部的庙坡剖面和熊坡东剖面中的砾石层在碎屑成分、重矿物和花岗岩砾石的地球化学成分等方面相似,应为古青衣江的产物,但其流向却与现代青衣江的流向不同,表明熊坡背斜是在大邑砾岩沉积之后隆起的,它的隆起迫使古青衣江改道。     

On the transport of small river run off by an alongshore baroclinic sea current

A numerical simulation has been undertaken to study the process of the transport of small river runoff by alongshore baroclinic sea currents. The study is based on the implementation of the Princeton Ocean Model (POM) under the conditions of a circular stratified basin whose surface is exposed to a transient tangential wind stress to form an alongshore baroclinic current. A baroclinic current of the downwelling type (in the Northern Hemisphere directed to the left to a sea-viewing observer) was shown to provide the carrying out of the river discharge from estuary’s vicinity more effectively than that of the upwelling type (in the Northern Hemisphere directed to the right to a sea-viewing observer).     

A field test of a linear stability model for crescentic bars

A morphodynamical linear stability analysis is used to predict the natural development of crescentic bed patterns and rip channels. The purpose is to investigate whether this technique, which is useful for understanding the physics of emerging bed-forms, can be used to make quantitative predictions in the field, which may then be of use for coastal engineers.     

Agricultural land use dynamics in the Brazilian Amazon based on remote sensing and census data

The potential impact of deforestation in the Brazilian Amazon on greenhouse gas emissions to the atmosphere calls for policies that take account of changes in forest cover. Although much research has focused on the location and effects of deforestation, little is known about the distribution and reasons for the agricultural uses that replace forest cover. We used Landsat TM-based deforestation and agricultural census data to generate maps of the distribution and proportion of four major agricultural land uses throughout the Brazilian Amazon in 1997 and 2007. We built linear and spatial regression models to assess the determinant factors of deforestation and those major agricultural land uses - pasture, temporary agriculture and permanent agriculture - for the states of Pará, Rondônia, and Mato Grosso. The data include 30 determinant factors that were grouped into two years (1996 and 2006) and in four categories: accessibility to markets, public policies, agrarian structure, and environment. We found an overall expansion of the total agricultural area between 1997 and 2007, and notable differences between the states of Pará, Rondônia, and Mato Grosso in land use changes during this period. Regression models for deforestation and pasture indicated that determinant factors such as distance to roads were more influential in 1997 than in 2007. The number of settled families played an important role in the deforestation and pasture, the effect was stronger in 2007 than 1997. Indigenous lands were significant in preventing deforestation in high-pressure areas in 2007. For temporary and permanent agricultures, our results show that in 1997 the effect of small farms was stronger than in 2007. The mapped land use time series and the models explain empirically the effects of land use changes across the region over one decade.     

Seismicity, seismic input and site effects in the Sahel—Algiers region (North Algeria)

Algiers city is located in a seismogenic zone. To reduce the impact of seismic risk in this Capital city, a realistic modelling of the seismic ground motion (SGM) is conducted by using the hybrid method that combines the finite differences method and the modal summation. For this purpose, a complete database of geological, geophysical and earthquake data is constructed. A critical re-appraisal of the seismicity of the zone [2.25°E–3.50°E, 36.50°N–37.00°N] is performed and an earthquake list, for the period 1359–2002, is compiled. The analysis of existing and newly retrieved macroseismic information allowed the definition of earthquake parameters of macroseismic events for which a degree of reliability is assigned. Geological cross sections have been built up to model the SGM in the city, caused by the 1989 Mont-Chenoua and the 1924 Douéra earthquakes. Synthetic seismograms and response spectral ratio is produced for Algiers, and they show that the soft sediments in Algiers centre are responsible of the noticed amplification of the SGM.     

Granitic plutonism as an indicator of microplates in the Palaeozoic of central and eastern Maine

Oxygen and strontium isotope ratios have been used to characterize source regions for granitic magmas for a transect across the northern Appalachian orogen in central and eastern Maine. The northwestern plutons (Katahdin and Seboeis) have δ¹⁸O values of 10.3–13.3 and initial ⁸⁷Sr/⁸⁶Sr ratios of 0.7083 and 0.7066, respectively. The central plutons (Bottle Lake and Center Pond) have lower δ¹⁸O values (8.2–9.9) and initial ⁸⁷Sr/⁸⁶Sr ratios (0.7043–0.7055). The southeastern plutons (Lucerne and Deblois) have δ¹⁸O values (9.0–11.0) but initial ⁸⁷Sr/⁸⁶Sr ratios (0.7077 and 0.7041, respectively) which are intermediate between the northwestern and central plutons.Source models derived from these results and other petrological and geochemical data reflect the juxtaposition of discrete source regions by transcurrent faulting, which may be related to oblique plate motions. This model illustrates the importance of microplate accretion in the Palaeozoic history of the northern Appalachian orogen.     

Oxygen isotope salt effects at high pressure and high temperature and the calibration of oxygen isotope geothermometers

The influence of NaCl, CaCl₂, and dissolved minerals on the oxygen isotope fractionation in mineral-water systems at high pressure and high temperature was studied experimentally. The salt effects of NaCl (up to 37 molal) and 5-molal CaCl₂ on the oxygen isotope fractionation between quartz and water and between calcite and water were measured at 5 and 15 kbar at temperatures from 300 to 750°C. CaCl₂ has a larger influence than NaCl on the isotopic fractionation between quartz and water. Although NaCl systematically changes the isotopic fractionation between quartz and water, it has no influence on the isotopic fractionation between calcite and water. This difference in the apparent oxygen isotope salt effects of NaCl must relate to the use of different minerals as reference phases. The term oxygen isotope salt effect is expanded here to encompass the effects of dissolved minerals on the fractionations between minerals and aqueous fluids. The oxygen isotope salt effects of dissolved quartz, calcite, and phlogopite at 15 kbar and 750°C were measured in the three-phase systems quartz-calcite-water and phlogopite-calcite-water. Under these conditions, the oxygen isotope salt effects of the three dissolved minerals range from ∼0.7 to 2.1‰. In both three-phase hydrothermal systems, the equilibrium fractionation factors between the pairs of minerals are the same as those obtained by anhydrous direct exchange between each pair of minerals, proving that the use of carbonate as exchange medium provides correct isotopic fractionations for a mineral pair.When the oxygen isotope salt effects of two minerals are different, the use of water as an indirect exchange medium will give erroneous fractionations between the two minerals. The isotope salt effect of a dissolved mineral is also the main reason for the observation that the experimentally calibrated oxygen isotope fractionations between a mineral and water are systematically 1.5 to 2‰ more positive than the results of theoretical calculations. Dissolved minerals greatly affect the isotopic fractionation in mineral-water systems at high pressure and high temperature. If the presence of a solute changes the solubility of a mineral, the real oxygen isotope salt effect of the solute at high pressure and high temperature cannot be correctly derived by using the mineral as reference phase.