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1.
Authigenic albites in carbonate rocks typically grow in a high-grade diagenetic to low-grade metamorphic environment and often show Roc-Tourné-twinning sensu Füchtbauer. Based on an investigation of four Middle to South European occurrences, they show Mn2+- and Fe3+-activated cathodoluminescence (CL), as revealed by combined high resolution spectroscopy of cathodoluminescence emission (HRS-CL), electron paramagnetic resonance (EPR), and proton-induced X-ray emission (μPIXE). 相似文献
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Mariëtte Wolthers Laurent Charlet Peter R. van der Linde 《Geochimica et cosmochimica acta》2005,69(14):3483-3492
Arsenate, As(V), sorption onto synthetic iron(II) monosulfide, disordered mackinawite (FeS), is fast. As(V) sorption decreases above the point of zero surface charge of FeS and follows the pH-dependent concentration of positively charged surface species. No redox reaction is observed between the As(V) ions and the mineral surface over the time span of the experiments. This observation shows that As(V) dominantly forms an outer-sphere complex at the surface of mackinawite. Arsenite, As(III), sorption is not strongly pH-dependent and can be expressed by a Freundlich isotherm. Sorption is fast, although slower than that of As(V). As(III) also forms an outer-sphere complex at the surface of mackinawite. In agreement with previous spectroscopic studies, complexation at low As(V) and As(III) concentration occurs preferentially at the mono-coordinated sulfide edge sites. The Kd (L g−1) values obtained from linear fits to the isotherm data are ∼9 for As(V) and ∼2 for As(III). Stronger sorption of As(V) than As(III), and thus a higher As(III) mobility, may be reflected in natural anoxic sulfidic waters when disordered mackinawite controls arsenic mobility. 相似文献
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Vanscheidt R. Bleul H. Manthey E. Jütte M. Pohlen M. Schmidtobreick L. Altmann M. Dieball A. Geffert M. Sanner J. Notni P. Schmoll J. 《Earth, Moon, and Planets》1998,81(3):223-231
Extensive widefield CCD direct imaging of C/1995 O1 (Hale-Bopp) at UBVRI was carried out at Hoher List Observatory with the
1.06 m telescope (field of view 20′ × 20′) and at Potsdam Observatory with the 0.70 m telescope (field of view 8′ × 8′). The
corresponding spatial resolution is 850–1000 km pix-1and 525–590 km pix-1, respectively. The data covers 25 nights from February 20 to April 21, 1997.
In order to quantify the various features in the apparent inner coma we introduce a new tomographic method that minimizes
the morphological bias caused by image processing. The tomographic analysis leads to quantitative maps refering to the position
and intensity of the dust ejections for each image frame. Variability and periodicity within the inner coma can be thoroughly
deduced due to various sets of consecutive nights in the observation period mentioned above. The results are compared with
applications of adaptive Laplace filtering.
This revised version was published online in July 2006 with corrections to the Cover Date. 相似文献
5.
A petrographic investigation revealed polyphase quartz cementation in the Finefrau Sandstone (Upper Carboniferous, Western Germany) and the Solling Sandstone (Lower Triassic, Central Germany). Three different cements could be distinguished in each sandstone based on their cathodoluminescence and trace element composition. The first quartz generation is suggested to have been formed during eogenesis due to dissolution and replacement of feldspar. The mesogenetic paragenesis comprises two generations of quartz and illite, which are accompanied by albite in the Solling Sandstone. Sharp luminescence zoning in quartz overgrowths points to distinct episodes of cementation in both sandstones. Significant amounts of Al, Li and H and traces of Ge and B have been detected in the quartz overgrowths. The Al‐content of the quartz cements in the Finefrau Sandstones exceeds that in the quartz cements in the Solling Sandstone by a factor of five. It is suggested that this compositional variation reflects the conditions in the pore‐water, such as temperature and pH. The Al‐concentration is generally correlated to the Li‐content with the exception of the latest quartz generation in the Finefrau Sandstones which is also most enriched in trace elements. The ratio of Li/Al varies between 0·11 and 0·25 in the two sandstones. The Li/H‐ratio, which ranges from 0·12 to 0·3, is controlled by the activity ratio of Li and H in the pore fluid. Clay minerals are the most important source for Li and high salinities favour the mobilization of Li during diagenesis. Thus, a relatively low salinity and low pH are responsible for the low Li/H‐ratio in the Finefrau Sandstone, while high salinity and neutral to alkaline pH results in a high Li/H‐ratio for the Solling Sandstone. The Ge‐contents are generally near the average of detrital quartz and indicate that pressure dissolution is a major source for quartz cementation. Different chemical compositions of distinct quartz generations indicate changes in the physico‐chemical conditions and point to mobilization of silica from different sources (for example, pressure solution and clay mineral transformations). 相似文献
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The 2220 Ma Kalahari Manganese field of South Africa is the world's largest Mn resource and a major producer. Current models for its origin rely on those developed for Phanerozoic deposits, invoking a submarine redox boundary and water movements across a continental shelf, precipitating Mn oxides from the sea. Here we report the discovery of major hydrothermal alteration in the thick andesitic volcanic pile beneath the Mn ore. This and other evidence shows that the Kalahari manganese is actually a volcanic exhalative deposit, analogous in some respects to those forming at present day mid-ocean ridges. Important differences in depth and oxygen supply account for the smaller area and high grade of the Kalahari Manganese Field, compared with the widespread but thinly developed modern ocean floor Mn deposits. 相似文献
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Surface chemistry of disordered mackinawite (FeS) 总被引：1，自引：0，他引：1
Mariëtte Wolthers Laurent Charlet David Rickard 《Geochimica et cosmochimica acta》2005,69(14):3469-3481
Disordered mackinawite, FeS, is the first formed iron sulfide in ambient sulfidic environments and has a highly reactive surface. In this study, the solubility and surface chemistry of FeS is described. Its solubility in the neutral pH range can be described by Ksapp = {Fe2+} · {H2S(aq)} · {H+}−2 = 10+4.87±0.27. Acid-base titrations show that the point of zero charge (PZC) of disordered mackinawite lies at pH ∼7.5. The hydrated disordered mackinawite surface can be best described by strongly acidic mono-coordinated and weakly acidic tricoordinated sulfurs. The mono-coordinated sulfur site determines the acid-base properties at pH < PZC and has a concentration of 1.2 × 10−3 mol/g FeS. At higher pH, the tricoordinated sulfur, which has a concentration of 1.2 × 10−3 mol/g FeS, determines surface charge changes. Total site density is 4 sites nm−2. The acid-base titration data are used to develop a surface complexation model for the surface chemistry of FeS. 相似文献
8.
Peter Haase Susanne Lohse Steffen Pauls Karin Schindehütte Andrea Sundermann Peter Rolauffs Daniel Hering 《Limnologica》2004,34(4):349-365
In the past, no single standardised method for sampling and sorting benthic macroinvertebrates has been implemented in Germany. Therefore, we tested the suitability of two common sorting protocols, RIVPACS and AQEM/STAR, by taking samples with each protocol at 44 sampling sites. Our results reveal that different methods deliver slightly different assessment results. Moreover these two methods differ in costs. Although the AQEM/STAR protocol takes longer than the RIVPACS protocol, we favoured the AQEM/STAR protocol because of its higher level of standardisation. In order to limit costs to an acceptable level, a modification of the AQEM/STAR protocol (MAS method) is developed. This method is highly standardised, gives stable assessment results and is relatively inexpensive (€ 224.00 for processing of an average sample). A detailed protocol of the newly developed method is given. 相似文献
9.
Michael Abratis Jonas Mädler Siegfried Hautmann Romain Meyer Lothar Viereck-Götte 《Chemie der Erde / Geochemistry》2007,67(2):133-150
New 40Ar/39Ar age data are determined for Cenozoic basaltic rocks from the Thuringian Rhön and Heldburg Gangschar (area also referred to as Grabfeld), integral parts of the Central European Volcanic Province. Applying the incremental heating technique on groundmass and plagioclase separates provided data which considerably specify our knowledge on the eruption ages in these volcanic fields and narrow down the duration of volcanic activity compared to earlier studies. All data but one outlier range between 20 and 14 Ma, being thus similar to those of the neighbouring Vogelsberg volcanic complex. The spectrum of ages is clearly divided into two distinct subsets: the Rhön ages are between 20 and 18 Ma, those of the Heldburg Gangschar are between 16 and 14 Ma. Thus, the present data clearly indicate a striking regional and temporal division of the Thuringian Miocene volcanism. The composition of the volcanic rocks in the two volcanic fields is remarkably diverse, ranging from tholeiitic basalts over alkali basalts and basanites to nephelinites. However, radiometric ages do not correlate with geochemical or petrological characteristics of the volcanics within each volcanic field, indicating that the different magma types erupted broadly contemporaneously.The outlier in age (29 Ma) is from a volcanic dyke of the NE Rhön area close to the NW end of the Thuringian Forest. However, more data are required to approve the significance of this age value, in particular since the rock showed isotopic age disturbance. 相似文献
10.
J. Götze M. Plötze Th. Götte R. D. Neuser D. K. Richter 《Mineralogy and Petrology》2002,76(3-4):195-212
Summary ?Sheet silicates of the serpentine–kaolin-group (serpentine, kaolinite, dickite, nacrite, halloysite), the talc–pyrophyllite-group
(talc, pyrophyllite), the smectite-group (montmorillonite), and illite (as a mineral of the mica-group) were investigated
to obtain information concerning their cathodoluminescence behaviour. The study included analyses by cathodoluminescence (CL
microscopy and spectroscopy), electron paramagnetic resonance (EPR), X-Ray diffraction (XRD), scanning electron microscopy
(SEM) and trace element analysis.
In general, all dioctahedral clay minerals exhibit a visible CL. Kaolinite, dickite, nacrite and pyrophyllite have a characteristic
deep blue CL, whereas halloysite emission is in the greenish-blue region. On the contrary, the trioctahedral minerals (serpentine,
talc) and illite do not show visible CL.
The characteristic blue CL is caused by an intense emission band around 400 nm (double peak with two maxima at 375 and 410 nm).
EPR measurements indicate that this blue emission can be related to radiation induced defect centres (RID), which occur as
electron holes trapped on apical oxygens (Si–O centre) or located at the Al–O–Al group (Al substituting Si in the tetrahedron).
Additional CL emission bands were detected at 580 nm in halloysite and kaolinite, and between 700 and 800 nm in kaolinite,
dickite, nacrite and pyrophyllite.
Time-resolved spectral CL measurements show typical luminescence kinetics for the different clay minerals, which enable differentiation
between the various dioctahedral minerals (e.g. kaolinite and dickite), even in thin section.
Received December 3, 2001; revised version accepted February 27, 2002 相似文献