This study examined the interaction between Cr(VI) and a Fe-rich soil in the presence of low-molecular-weight organic acids
as a function of pH. Oxalic and tartaric acids were chosen since they existed in soils commonly. Batch experiments showed
that adsorption of Cr(VI) by the soil within the pH range examined was inhibited in the presence of oxalic acid, which was
more pronounced when the initial ratio of [oxalic acid]/[Cr(VI)] was raised from 1:1 to 2:1. With the addition of tartaric
acid, concentration of Cr(VI) in equilibrium solutions was far less than that of single adsorbate system across the pH wide
(2.5–5.5), which was noticeable especially at low pH. The results were attributed to Cr(VI) adsorption and, particularly,
the soil surface catalyzed reduction of Cr(VI) to Cr(III) by tartaric acid. The data reported in this paper suggested that
the mobility, the bioavailability, and the toxicity of Cr(VI) in soil environments might be greatly affected by pH, the presence
and nature of low-weight-molecular organic acids (oxalic and tartaric acids). 相似文献
The Gföhl Unit is the largest migmatite terrain of the Variscan orogenic root domain in Europe. Its genesis has been until now attributed to variable degrees of in situ partial melting. In the Rokytná Complex (Gföhl Unit, Czech Republic) there is a well-preserved sequence documenting the entire migmatitization process on both outcrop and regional scales. The sequence starts with (i) banded orthogneiss with distinctly separated monomineralic layers, continuing through (ii) migmatitic mylonitic gneiss, (iii) schlieren migmatite characterised by disappearance of monomineralic layering and finally to (iv) felsic nebulitic migmatite with no relics of the original banding.
While each type of migmatite shows a distinct whole-rock geochemical and Sr–Nd isotopic fingerprint, the whole sequence evolves along regular, more or less smooth trends for most of the elements. Possible mechanisms which could account for such a variation are that the individual migmatite types (i) are genetically unrelated, (ii) originated by equilibrium melting of a single protolith, (iii) formed by disequilibrium melting (with or without a small-scale melt movement) or (iv) were generated by melt infiltration from external source. The first scenario is not in agreement with the field observations and chemistry of the orthogneisses/migmatites. Neither of the remaining hypotheses can be ruled out convincingly solely on whole-rock geochemical grounds. However in light of previously obtained structural, petrologic and microstructural data, this sequence can be interpreted as a result of a process in which the banded orthogneiss was pervasively, along grain boundaries, penetrated by felsic melt derived from an external source.
In terms of this melt infiltration model the individual migmatites can be explained by different degrees of equilibration between the bulk rock and the passing melt. The melt infiltration can be modelled as an open-system process, characterised by changes of the total mass/volume and accompanied by gains/losses in many of the major- and trace elements. The modelling of the mass balance resulted in identification of a component added by a heterogeneous nucleation of feldspars, quartz and apatite from the passing melt. This is in line with the observed presence of new albitic plagioclase, K-feldspar and quartz coatings as well as resorption of relict feldspars. At the most advanced stages (schlieren and nebulitic migmatites) the whole-rock trace-element geochemical variations document an increasing role for fractional crystallization of the K-feldspar and minor plagioclase, with accessory amounts of monazite, zircon and apatite.
The penetrating melt was probably (leuco-) granitic, poor in mafic components, Rb rich, with low Sr, Ba, LREE, Zr, U and Th contents. It probably originated by partial melting of micaceous quartzo-feldspathic rocks.
If true and the studied migmatites indeed originated by a progressive melt infiltration into a single protolith resembling the banded orthogneiss, this until now underappreciated process would have profound implications regarding rheology and chemical development of anatectic regions in collisional orogens. 相似文献
The Yenice–Gönen Fault (YGF) is one of the most important active tectonic structures in the Biga peninsula. On March 18, 1953, a destructive earthquake (Mw = 7.2) occurred on the YGF, which is considered to be a part of the southern branch of the North Anatolian Fault Zone (NAFZ). A 70 km-long dextral surface rupture formed during the Yenice–Gönen Earthquake (YGE).In this study, structural and palaeoseismological features of the YGF have been investigated. The YGF surface ruptures have been mapped and three trenches were excavated at Muratlar, Karaköy and Seyvan sites.According to the palaeoseismic interpretation and the results of 14C AMS dating, Seyvan trench shows that an earthquake of palaeoseismic age ca. 620 AD ruptured a different strand of the 1953 fault, producing rather significant surface rupture displacement, while there are indications that at least two older events occurred during the past millennia. Another set of trenches excavated near Gönen town (Muratlar village) revealed extensive liquefaction not only during the 1953 event, but also during a previous earthquake, dated at 1440 AD. The Karaköy trench shows no indications of recent reactivations.Based on the trenching results, we estimate a recurrence interval of 660 ± 160 years for large morphogenic earthquakes, creating linear surface ruptures. The maximum reported displacement during the 1953 earthquake was 4.2 m. Taking into account the palaeoseismologically determined earthquake recurrence interval and maximum displacement, slip-rate of the YGF has been calculated to be 6.3 mm/a, which is consistent with present-day velocities determined by GPS measurements. According to the geological investigations, cumulative displacement of the YGF is 2.3 km. This palaeoseismological study contributes to model the behaviour of large seismogenic faults in the Biga Peninsula. 相似文献
An attempt has been made to understand the potential of temporal Advanced Wide Field Sensor (AWiFS) data aboard IRS-P6 (Resourcesat) to generate the land use land cover information along with the net sown area. The temporal data sets were georeferenced, converted to top of atmosphere reflectance and classified using decision tree classifier, See5. Results indicate that the temporal data set could give a better definition of training sites thereby resulting in good overall kappa (kappa = 0.8651) as well as individual classification accuracies. However, co-registration of temporal datasets accuracies also has got a significant influence on the classification accuracy. Temporal variation in cloud infestation and availability of appropriate data sets within the season (before harvest of the crop) has also affected the classification accuracy. 相似文献
Chromium (Cr) is a heavy metal that exists in soils in two stable oxidation states, +III and +VI. The trivalent species is an essential nutrient, whereas the hexavalent species is highly toxic. This study investigated the environmental impact of CrIII potentially released into soil from wastes and various materials by determining the risk of oxidation of initially soluble inorganic CrIII into hazardous CrVI. The principal aim was to describe the pH-dependent mechanisms that regulate 1) the formation of CrVI from the easily soluble CrIII and 2) the potential bioavailability of CrIII and that of CrVI species produced in the oxidation of CrIII in agricultural soil (fine sand, organic carbon 3.2%). The amount of CrVI formed in oxic soil conditions was regulated by two counteracting reactions: 1) oxidation of CrIII into CrVI by manganese oxide (MnIVO2) and 2) the subsequent reduction of CrVI by organic matter back to CrIII. The effect of pH on this net-oxidation of CrIII and on the chemical availability of both CrIII and CrVI species was investigated in soil samples incubated with or without excessive amounts of synthetic MnO2, over the chemically adjusted pH range of 3.9–6.3 (+22 °C, 47 d). In soil subsamples without added MnO2, the net-oxidation of CrIII into CrVI (1 mM CrCl3 in soil suspensions, 1:10 w/V) was negligible. As for the MnO2-treated soils, at maximum only 4.7% of added CrIII was oxidized – regardless of the high oxidation potential of these subsamples. The lowest production of CrVI was observed under acidic soil conditions at pH ∼4. At low pH, the net-oxidation diminished as result of enhanced reduction of CrVI back to CrIII. At higher pHs, the oxidation was limited by enhanced precipitation (or adsorption) of CrIII, which lowered the overall amount of CrIII susceptible for oxidation. Moreover, the oxidation reactions by MnO2 were inhibited by formation of Cr(OH)3 coverage on its surface. The pH-dependent chemical bioavailability of added CrIII differed from that of the CrVI formed. At elevated pHs the chemical availability of CrIII decreased, whereas that of CrVI produced increased. However, the risk of CrVI formation through oxidation of the easily soluble inorganic CrIII was considered to be low in agricultural soils high in organic matter and low in innate MnO2. 相似文献
Previous studies have examined the projected climate types in China by 2100. This study identified the emergence time of climate shifts at a 1?scale over China from 1990 to 2100 and investigated the temporal evolution of K o¨ppen–Geiger climate classifications computed from CMIP5 multi-model outputs. Climate shifts were detected in transition regions(7%–8% of China's land area) by 2010, including rapid replacement of mixed forest(Dwb) by deciduous forest(Dwa) over Northeast China, strong shrinkage of alpine climate type(ET) on the Tibetan Plateau, weak northward expansion of subtropical winterdry climate(Cwa) over Southeast China, and contraction of oceanic climate(Cwb) in Southwest China. Under all future RCP(Representative Concentration Pathway) scenarios, the reduction of Dwb in Northeast China and ET on the Tibetan Plateau was projected to accelerate substantially during 2010–30, and half of the total area occupied by ET in 1990 was projected to be redistributed by 2040. Under the most severe scenario(RCP8.5), sub-polar continental winter dry climate over Northeast China would disappear by 2040–50, ET on the Tibetan Plateau would disappear by 2070, and the climate types in 35.9%and 50.8% of China's land area would change by 2050 and 2100, respectively. The results presented in this paper indicate imperative impacts of anthropogenic climate change on China's ecoregions in future decades. 相似文献