Calcium isotope (δCa) fractionation along hydrothermal pathways, Logatchev field (Mid-Atlantic Ridge, 14°45′N)     

Marghaleray Amini  Anton Eisenhauer  Florian Böhm  Wolfgang Bach  Martin Rosner  Barbara Bock  Folkmar Hauff 《Geochimica et cosmochimica acta》2008,72(16):4107-4122

We investigate the Logatchev Hydrothermal Field at the Mid-Atlantic Ridge, 14°45′N to constrain the calcium isotope hydrothermal flux into the ocean. During the transformation of seawater to a hydrothermal solution, the Ca concentration of pristine seawater ([Ca]_SW) increases from about 10 mM to about 32 mM in the hydrothermal fluid endmember ([Ca]_HydEnd) and thereby adopts a δ^44/40Ca_HydEnd of −0.95 ± 0.07‰ relative to seawater (SW) and a ⁸⁷Sr/⁸⁶Sr isotope ratio of 0.7034(4). We demonstrate that δ^44/40Ca_HydEnd is higher than that of the bedrock at the Logatchev field. From mass balance calculations, we deduce a δ^44/40Ca of −1.17 ± 0.04‰ (SW) for the host-rocks in the reaction zone and −1.45 ± 0.05‰ (SW) for the isotopic composition of the entire hydrothermal cell of the Logatchev field. The values are isotopically lighter than the currently assumed δ^44/40Ca for Bulk Earth of −0.92 ± 0.18‰ (SW) [Skulan J., DePaolo D. J. and Owens T. L. (1997) Biological control of calcium isotopic abundances in the global calcium cycle. Geochim. Cosmochim. Acta61,(12) 2505-2510] and challenge previous assumptions of no Ca isotope fractionation between hydrothermal fluid and the oceanic crust [Zhu P. and Macdougall J. D. (1998) Calcium isotopes in the marine environment and the oceanic calcium cycle. Geochim. Cosmochim. Acta62,(10) 1691-1698; Schmitt A. -D., Chabeaux F. and Stille P. (2003) The calcium riverine and hydrothermal isotopic fluxes and the oceanic calcium mass balance. Earth Planet. Sci. Lett. 6731, 1-16]. Here we propose that Ca isotope fractionation along the fluid flow pathway of the Logatchev field occurs during the precipitation of anhydrite. Two anhydrite samples from the Logatchev Hydrothermal Field show an average fractionation of about Δ^44/40Ca = −0.5‰ relative to their assumed parental solutions. Ca isotope ratios in aragonites from carbonate veins from ODP drill cores indicate aragonite precipitation directly from seawater at low temperatures with an average δ^44/40Ca of −1.54 ± 0.08‰ (SW). The relatively large fractionation between the aragonite precipitates and seawater in combination with their frequent abundance in weathered mafic and ultramafic rocks suggest a reconsideration of the marine Ca isotope budget, in particular with regard to ocean crust alteration.  相似文献   

Phytoreduction and volatilization of mercury by ascorbate in Arabidopsis thaliana, European beech and Norway spruce     

Florian Battke  Dieter Ernst  Frank Fleischmann  Stefan Halbach 《Applied Geochemistry》2008

Mercury vapor (Hg⁰) emission from plants contributes to the atmospheric Hg cycle. Young barley (Hordeum vulgare L.) plants grown on a hydroponic cultivation medium containing Hg(II) have previously been shown to increase their Hg⁰ emission significantly by reduction of Hg(II) with endogenous ascorbic acid. Regarding the potential contribution to the Hg cycle from the vast forest-covered areas, it was important to investigate this mechanism in trees. The increase in Hg⁰ emission from young European beech plants cultivated on a HgCl₂ medium exceeded that from controls by ca. tenfold and was proportional to the Hg(II) concentration. From these experiments, a flux of 12.8 μg Hg⁰/h/m² was estimated at an exposure of the roots to 20 μM Hg(II). Mercury vapor release from homogenates of Norway spruce needles exceeded that from European beech leaves by a factor of 2.3–4, i.e. in proportion to the reported AA concentrations; the reduction was maximal at alkaline pH which is typical for AA. The 8.4-fold difference in Hg⁰ release between homogenates from wild-type Arabidopsis thaliana and from its AA-deficient mutant vtc 1-1 also paralleled the reported difference in AA levels of both species. It is concluded that the phytoreduction and vaporization of Hg by AA is an important mechanism as much for Hg detoxification in trees as for Hg emission to the atmosphere. The efficiency of this process seems to result from the optimal coordination of transfer and biochemical transformation of mercuric ions and Hg vapor. There is no evidence for a relevant difference in the mechanisms of biogenic Hg(II) reduction between grass plants and trees.  相似文献   

Präparationstechnik für Aufbereitungsprodukte zur quantitativen erzmikroskopischen Untersuchung     

Gerhard Ludwig 《Mineralium Deposita》1966,1(3):193-200

Zusammenfassung Mikroskopische Anschliffe feinkörniger Aufbereitungsprodukte können nur dann quantitativ ausgewertet werden, wenn ihre Schliffqualität so hoch ist, daß auch feinste Partien sicher zu bestimmen sind. Daneben muß gewährleistet sein, daß die an der Schliffoberfläche erfaßten Körner die tatsächliche Verteilung der Mineralien der Probe repräsentieren. Diese Forderung kann nur durch zweckentsprechende Präparation, die dem eigentlichen Schleif- und Polierprozeß vorausgeht, erfüllt werden. Als günstigste Lösung erscheint es, das Korngemisch exakt als Einkornschicht zu präparieren und anschließend wie Stückproben anzuschleifen. Die Schliffe können dann nach den gleichen statistischen Gesetzmäßigkeiten ausgewertet werden, wie sie bei praktisch zweidimensionalen Dünnschliffen oder bei Streupräparaten nichtopaker Korngemische vorliegen.

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Quantitative examination of fine-grained ore dressing products depends on good quality of the sections and on whether very small particles and areas of grains can be determined. Besides, it must absolutely be guaranteed that the grains at the section surface represent the actual distribution of the minerals in the sample. This condition can only be realized by suitable grain mounting prior to grinding and polishing. The best method for this purpose appears to be the preparation of a mono-grain layer. The polished sections can then be examined according to the same statistical laws as two-dimensional thin sections or immersion-liquid slides of non-opaque mixtures of grains.

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Mitteilung Nr. 141 aus dem Forschungsinstitut für Aufbereitung der Deutschen Akademie der Wissenschaften zu Berlin, Freiberg (Sachsen). Direktor: Prof. Dr.-Ing. habil. H. Kirchberg.  相似文献   

Trace element diagenesis in pyrite-rich sediments of the Achterwasser lagoon, SW Baltic Sea     

Florian Scholz  Thomas Neumann 《Marine Chemistry》2007,107(4):516-532

The early diagenesis of trace elements (V, Cr, Co, Cu, Zn, As, Cd, Ba, U) in anoxic sediments of the Achterwasser, a shallow lagoon in the non-tidal Oder estuary in the Baltic Sea, was investigated in the context of pyrite formation. The dissolved major redox parameters show a two-tier distribution with transient signals in the occasionally re-suspended fluid mud layer (FM) and a permanently established diagenetic sequence in the sediment below. Intense microbial respiration leads to rapid depletion of O₂ within the uppermost mm of the FM. The reduction zones of Mn, Fe and sulfate overlap in the FM and in the permanently anoxic sediment section which appears to be a typical feature of estuarine sediments, under low-sulfate conditions. Degrees of pyritization (DOP) range from 50% in the FM to remarkably high values > 90% at 50 cm depth. Pyrite formation at the sediment surface is attributed to the reaction of Fe-monosulfides with intermediate sulfur species via the polysulfide pathway. By contrast, intense pyritization in the permanently anoxic sediment below is attributed to mineral growth via adsorption of aqueous Fe-sulfide complexes onto pyrite crystals which had originally formed in the surface layer.The studied trace elements show differential behavior patterns which are closely coupled to the diagenetic processes described above: (i) Zn, Cu and Cd are liberated from organic matter in the thin oxic layer of the sediment and diffuse both upwards across the sediment/water boundary and downwards to be trapped as monosulfides, (ii) V, Cr, Co and As are released during reductive dissolution of Mn- and Fe-oxyhydroxides, (iii) U removal from pore water occurs concomitantly to Fe reduction in the FM and is attributed to reduction of U(VI) to U(IV), (iv) the Ba distribution is controlled by reductive dissolution of authigenic barite in the sulfate reduction zone coupled with upward diffusion and re-precipitation. The incorporation of trace elements into pyrite is most intense for Co, Mn and As, intermediate for Cu and Cr and little to negligible for U, Zn, Cd, V and Ba. The observed trend is largely in agreement with previous studies and may be explained with differing rates for ligand exchange. Slow and fast ligand exchange and thus precipitation kinetics are also displayed by downcore increasing (Mn, Cr, Co and As) or constantly low (Zn, Cu, Cd) pore water concentrations. The downward increasing degrees of trace metal pyritization (DTMP) for Co, Cu, Zn and As are, in analogy to pyrite growth, assigned to adsorption of sulfide complexes or As oxyanions onto preexisting pyrite minerals.  相似文献   

Composition-Induced Variations in SIMS Instrumental Mass Fractionation during Boron Isotope Ratio Measurements of Silicate Glasses     

Martin Rosner  Michael Wiedenbeck  Thomas Ludwig 《Geostandards and Geoanalytical Research》2008,32(1):27-38

An analytical artefact is reported here related to differences in instrumental mass fractionation between NIST SRM glasses and natural geological glasses during SIMS boron isotope determinations. The data presented demonstrated an average 3.4‰ difference between the NIST glasses and natural basaltic to rhyolitic glasses mainly in terms of their sputtering-induced fractionation of boron isotopes. As no matrix effect was found among basaltic to rhyolitic glasses, instrumental mass fractionation of most natural glass samples can be corrected by using appropriate glass reference materials. In order to confirm the existence of the compositionally induced variations in boron SIMS instrumental mass bias, the observed offset in SIMS instrumental mass bias has been independently reproduced in two laboratories and the phenomenon has been found to be stable over a period of more than one year. This study highlights the need for a close match between the chemical composition of the reference material and the samples being investigated.  相似文献   

Solar irradiance modulation by active regions during 1980     

Sabatino Sofia  Ludwig Oster  Kenneth Schatten 《Solar physics》1982,80(1):87-98

The solar irradiance modulation due to active regions during 1980 has been investigated in detail. Specifically, we estimate the uncertainties caused by ground-based data used as input in the modeling effort, and by our currently incomplete knowledge of the proper parameters that describe the angular variation of sunspot and facular contrasts. We conclude that the most significant uncertainties are due to errors in area measurements and, possibly, varying spot and facular brightness. A standard model for later use is derived by a best-fit technique of the currently available ACRIM irradiance data and the predictions of our models with appropriately varied parameters. Finally, we compute the expected irradiance for the entire year of 1980.NRC Senior Research Associate on leave from the Joint Institute for Laboratory Astrophysics and the Astro-Geophysics Department, University of Colorado at Boulder, Colo., U.S.A.  相似文献   

Crustal structure of the Eastern Alps along the TRANSALP profile from wide-angle seismic tomography   总被引：1，自引：1，他引：1  

Florian Bleibinhaus  Helmut Gebrande 《Tectonophysics》2006,414(1-4):51

The objective of the TRANSALP project is an investigation of the Eastern Alps with regard to their deep structure and dynamic evolution. The core of the project is a 340-km-long seismic profile at 12°E between Munich and Venice. This paper deals with the P-wave velocity distribution as derived from active source travel time tomography. Our database consists of Vibroseis and explosion seismic travel times recorded at up to 100 seismological stations distributed in a 30-km-wide corridor along the profile. In order to derive a velocity and reflector model, we simultaneously inverted refractions and reflections using a derivative of a damped least squares approach for local earthquake tomography. 8000 travel time picks from dense Vibroseis recordings provide the basis for high resolution in the upper crust. Explosion seismic wide-angle reflection travel times constrain both deeper crustal velocities and structure of the crust–mantle boundary with low resolution. In the resulting model, the Adriatic crust shows significantly higher P-wave velocities than the European crust. The European Moho is dipping south at an angle of 7°. The Adriatic Moho dips north with a gentle inclination at shallower depths. This geometry suggests S-directed subduction. Azimuthal variations of the first-break velocities as well as observations of shear wave splitting reveal strong anisotropy in the Tauern Window. We explain this finding by foliations and laminations generated by lateral extrusion. Based on the P-wave model we also localized almost 100 local earthquakes recorded during the 2-month acquisition campaign in 1999. Seismicity patterns in the North seem related to the Inn valley shear zone, and to thrusting of Austroalpine units over European basement. The alignment of deep seismicity in the Trento-Vicenza region with the top of the Adriatic lower crust corroborates the suggestion of a deep thrust fault in the Southern Alps.  相似文献   

Permanent Scatterers for landslide investigations: outcomes from the ESA-SLAM project   总被引：3，自引：0，他引：3  

Paolo Farina  Davide Colombo  Alfio Fumagalli  Florian Marks  Sandro Moretti 《Engineering Geology》2006,88(3-4):200-217

Within the SLAM project (Service for Landslide Monitoring), launched in 2003 by the European Space Agency (ESA) the Permanent Scatterers (PS) technique, a multi-image interferometric approach, coupled with the interpretation of aerial-photos and optical satellite images, was carried out for landslide investigations. The PS analysis was applied at a regional scale as support for landslide inventory mapping and at local scale for the monitoring of single well-known slope movements. For the integration of the PS measurements within a landslide inventory the Arno river basin (Italy) was chosen as test site for the presence of a high number of mass movements (to date about 300 areas at high landslide risk and more than 27,000 individual landslides mapped by the institutional authorities). About 350 SAR images have been interferometrically processed by means of the PS technique, with the detection of about 600,000 PS. The use of optical images contributed spatial meaning to the point-wise information provided by the PS, making it easier to identify terrain features related to slope instability and the landslide boundaries. Here we describe the employed methodology and its impact in the updating of a preexisting landslide inventory. 6.8% of the total number of landslides were characterized by ground displacement measurements from the PS: 6.1% of already mapped landslides and 0.8% of new unstable areas detected through the PS analysis. Moreover, most of the PS are located in urban areas, showing that the proposed methodology is suitable for landslide mapping in areas with a quite high density of urbanization, but that over vegetated areas it still suffers from the limitations induced by the current space-borne SAR missions (e.g. temporal de-correlation). On the other hand, the use of InSAR for the monitoring of single slow landslides threatening built-up areas has provided satisfactory results, allowing the measurement of superficial deformations with high accuracy on the landslide sectors characterized by a good radar reflectivity and coherence.  相似文献   

The origin of reaction textures in mantle peridotite xenoliths from Sal Island, Cape Verde: the case for “metasomatism” by the host lava   总被引：1，自引：1，他引：1  

Cliff S. J. Shaw  Florian Heidelbach  Donald B. Dingwell 《Contributions to Mineralogy and Petrology》2006,151(6):681-697

Reaction zones around minerals in mantle xenoliths have been reported from many localities worldwide. Interpretations of the origins of these textures fall into two groups: mantle metasomatic reaction or reaction during transport of the xenoliths to the surface. A suite of harzburgitic mantle xenoliths from Sal, Cape Verde show clear evidence of reaction during transport. The reactions resulted in the formation of olivine–clinopyroxene and Si- and alkali-rich glass reaction zones around orthopyroxene and sieve-textured clinopyroxene and sieve textured spinel, both of which are associated with a Si- and alkali-rich glass similar to that in the orthopyroxene reaction zones. Reaction occurred at pressures less than the mantle equilibration pressure and at temperatures close to the liquidus temperature of the host magma. In addition, there is a clear spatial relation of reaction with the host lava: reaction is most intense near the lava/xenolith contact. The residence time of the xenoliths in the host magma, determined from Fe–Mg interdiffusion profiles in olivine, was approximately 4 years. Our results cannot be reconciled with a recent model for the evolution of the mantle below the Cape Verde Archipelago involving mantle metasomatism by kimberlitic melt. We contend that alkali-rich glasses in the Sal xenoliths are not remnants of a kimberlitic melt, but rather they are the result of reaction between the host lava or a similar magma and xenolith minerals, in particular orthopyroxene. The formation of a Si- and alkali-rich glass by host magma–orthopyroxene reaction appears to be a necessary precursor to formation of sieve textured spinel and clinopyroxene.  相似文献   

A Permeable Reactive Barrier for Treatment of Heavy Metals   总被引：8，自引：0，他引：8  

Ralph D. Ludwig  Rick G. McGregor  David W. Blowes  Shawn G. Benner  Keith Mountjoy 《Ground water》2002,40(1):59-66

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