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Complex Mo,V‐based mixed oxides that crystallize in the orthorhombic M1‐type structure are promising candidates for the selective oxidation of small alkanes. The oxygen sublattice of such a complex oxide has been studied by annular bright field scanning transmission electron microscopy. The recorded micrographs directly display the local distortion in the metal oxygen octahedra. From the degree of distortion we are able to draw conclusions on the distribution of oxidation states in the cation columns at different sites. The results are supported by X‐ray diffraction and electron paramagnetic resonance measurements that provide integral details about the crystal structure and spin coupling, respectively.  相似文献   
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Summary Enzyme electrodes were assembled by coupling membrane-immobilized lactate monooxygenase and coimmobilized lactate monooxygenase and lactate dehydrogenase, respectively, to oxygen electrodes. The lactate monooxygenase sensor was used for lactate determination with the analyzer Glukometer as well as for sequential measurement of lactate and lactate dehydrogenase activity.The bienzyme electrode is applicable for determining lactate and pyruvate in one measuring cycle. The operational parameters of the optimized sensors like measuring range, relative standard deviation, measuring frequency, and stability were studied. Determinations in biological fluids correlated well with spectrophotometric reference methods.  相似文献   
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The two elementsχ′ yx andχ″ xx of the magnetic susceptibility tensor for the cubic ferromagnetic EuO are investigated at microwave frequencies. It is shown that these two elements coincide when the magnetic field is large enough to remove the domain structure within the sample. This is in coincidence with theoretical predictions and shows a certain structure of the Hamiltonian. The magnetic transition temperature is found to beT c=(69.2±0.2)°K in agreement with the result from specific heat measurement.  相似文献   
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The variation of the natural 15N abundance is often used to evaluate the origin of nitrogen or the pathways of N input into ecosystems. We tried to use this approach to assess the main input pathways of nitrogen into the sand dune area of the north-western Negev Desert (Israel). The following two pathways are the main sources for nitrogen input into the system:
  1. Biological fixation of atmospheric nitrogen by cyanobacteria present in biological crusts and by N2-fixing vascular plants (e.g. the shrub Retama raetam);

  2. Atmospheric input of nitrogen by wet deposition with rainfall, dry deposition of dust containing N compounds, and gaseous deposition.

Samples were taken from selected environmental compartments such as biological crusts, sand underneath these crusts (down to a depth of 90?cm), N2-fixing and non-N2-fixing plants, atmospheric bulk deposition as well as soil from arable land north of the sandy area in three field campaigns in March 1998, 1999 and 2000. The δ15N values measured were in the following ranges: grass ?2.5‰ to +1.5‰; R. reatam: +0.5‰ to +4.5‰; non-N2-fixing shrubs +1‰ to +7‰; sand beneath the biological crusts +4‰ to +20‰ (soil depth 2–90?cm); and arable land to the north up to 10‰. Thus, the natural 15N abundance of the different N pools varies significantly. Accordingly, it should be feasible to assess different input pathways from the various 15N abundances of nitrogen. For example, the biological N fixation rates of the Fabaceae shrub R. reatam from the 15N abundances measured were calculated to be 46–86% of biomass N derived from the atmosphere. The biological crusts themselves generally show slight negative 15N values (?3‰ to ?0.5‰), which can be explained by biological N fixation. However, areas with a high share of lichens, which are unable to fix atmospheric nitrogen, show very negative values down to ?10‰. The atmospheric N bulk deposition, which amounts to 1.9–3.8?kg?N/ha?yr, has a 15N abundance between 4.4‰ and 11.6‰ and is likely to be caused by dust from the arable land to the north. Thus, it cannot be responsible for the very negative values of lichens measured either. There must be an additional N input from the atmosphere with negative δ15N values, e.g. gaseous N forms (NO x , NH3). To explain these conflicting findings, detailed information is still needed on the wet, particulate and gaseous atmospheric deposition of nitrogen.  相似文献   
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