Geochemical profiles in pore water of marine sediments have been considered as, important indicators of gas hydrate occurrence. In the gas hydrate area around the world, the decrease of sulfate, calcium, and magnesium concentrations with depth mainly results directly or indirectly from the anaerobic oxidation of methane (AOM). The ubiquitous abnormally high concentration gradients of iodide in the research area reflect the large methane-generating potential of the area. Thus, we explore the feasibility of using gradients of sulfate, iodide, and authigenic carbonate precipitation as indicators for gas hydrate in the regional exploration of gas hydrate formation. We test the criterion in the gas hydrate zone in the South China Sea (SCS) for the recognition of gas hydrate by using the gradients of sulfate, calcium plus magnesium, and iodide. Contour maps of pore-water gradients from expeditions in the study area are used to correlate the key gradients to underlying gas hydrate occurrence. The results show that the largest potential gas hydrate indicated by the contour maps of the indicators are well consistent with the discovery of GMGS1 and GMGS3 expedition. It implies the possible applicability of this geochemical method in gas hydrate exploration. Also, we identify a promising area in the South China Sea for future gas hydrate investigations. It is the first collective application of the gradients of sulfate, calcium plus magnesium, and iodide to a gas hydrate terrane, especially to a large area of the SCS. We believe that the result of this research will benefit the future exploration of gas hydrate and will arouse a lot of interest from other researchers.
The location of the grounding grid conductors is critical for performing corrosion diagnosis and maintenance work. An improved magnetic field differential method to locate the unknown grounding grid based on truncation errors and the round-off errors analysis is presented in this paper. It was proven that a different order of the magnetic field derivative can be used to determine the position of the grounding conductor according to the peak value of the derivative. Due to the accumulative error of higher differentiation, the truncation error and rounding error were used to analyze to accumulative error and to determine the optimal step size to measure and calculate the higher differentiation. The possible range and probability distribution of the two kinds of errors at each order are described, and the index of peak position error was derived, which can be used to locate the grounding conductor in the power substation.
Fluorescence imaging is considered as one of the most powerful techniques for monitoring biomolecule activities in living systems. Near-infrared (NIR) light is advantageous for minimum photodamage, deep tissue penetration, and minimum background autofluorescence interference. Herein, we have developed a new NIR fluorescent dye, namely, RB-1, based on the Rhodamine B scaffold. RB-1 exhibits excellent photophysical properties including large absorption extinction coefficients, high fluorescence quantum yields, and high photostability. In particular, RB-1 displays both absorption and emission in the NIR region of the "biological window" (650-900 nm) for imaging in biological samples. RB-1 shows absorption maximum at 614 nm (500-725 nm) and emission maximum at 712 nm (650-825 nm) in ethanol, which is superior to those of traditional rhodamine B in the selected spectral region. Furthermore, applications of RB-1 for fluorescence imaging in living cells and small animals were investigated using confocal fluorescence microscopy and in vivo imaging system with a high signal-to-noise ratio (SNR = 10.1).
Frequency domain spectroscopy (FDS) is widely used in analysis of insulation condition of dielectric material. The traditional contact method is susceptible to the impact of the contact state between the test sample and the electrode, which is also difficult to ensure the accuracy and repeatability of the test results. Using the method of sputtering gold on the surface of the sample is an effective way to avoid this problem though, this processing method is time-consuming and high-cost. This paper presents a method based on limit fitting by neural network to realize contact-free dielectric response measurement, which can eliminate the distortion effect of the air gap introduced by the uneven surface of dielectric material. Cross linked polyethylene (XLPE) is chosen as the test object to verify this method: in the domain of frequency = 1-1000 Hz, comparing with the test results of sample treatment by gold sputtering, the average error of frequency domain spectroscopy data in traditional method is 10%, while the new method is only 1%. Meanwhile, this paper analyses the cause of the errors in each method. This is an open access article under the terms of the Creative Commons Attribution License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
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