On the Aspect Sensitivity of Radio Aurora

1972 ◽  
Vol 50 (21) ◽  
pp. 2557-2564 ◽  
Author(s):  
D. R. McDiarmid

Previous measurements of the aspect sensitivity of radio aurora at VHF have yielded two distinctly different values, namely, 10 dB/deg and 1 to 2 dB/deg. In this paper, a previously discussed event is re-analyzed in greater detail in an attempt to resolve this apparent anomaly. The results of this analysis, which takes account of the effects of a number of measurement errors and uncertainties, lead to the conclusion that the aspect sensitivity of the event could not have been greater than [Formula: see text] in the aspect angle interval of approximately 4.5° to 19.5°. The most likely value is between 1.3 and 1.5 dB/deg. It is suggested that the two observed aspect sensitivity curves correspond to different radio aurora producing mechanisms.

2013 ◽  
Vol 30 (2) ◽  
pp. 245-259 ◽  
Author(s):  
Jenn-Shyong Chen ◽  
Jun-ichi Furumoto

Abstract The aspect angle, a measurement of the aspect sensitivity of atmospheric refractivity irregularities, was estimated with multiple-receiver coherent radar imaging (CRI) of very high frequency (VHF) atmospheric radar. Two CRI parameters retrieved by Capon’s method were utilized to derive the aspect angle: brightness width from the vertical radar beam and the direction of arrival (DOA) of the echo center from the oblique radar beam. Differing from previous studies with CRI, the radar beam weighting effect on the CRI brightness distribution was considered, and moreover, the radar beamwidth used in study was adaptive to the signal-to-noise ratio (SNR) of data as well as the off-beam direction angle. The study is based on statistical results. It is shown that the brightness width, a representative of the aspect angle, obtained from the modified CRI brightness distribution of the vertical radar beam was generally larger than that without correction, and it was very close to the values derived from the DOA of the 1° oblique radar beam and the power distribution of multiple beam directions. Moreover, the aspect angle derived from the DOA varied with the radar beam direction, which was similar to that obtained from the comparison of echo powers of a radar beam pair; however, the DOA approach yielded a much larger aspect angle in the low-SNR condition. This study recommended a feasibility of improving the measurements of atmospheric parameters with CRI after removing the radar beam weighting effect suitably from the CRI brightness distribution.


Author(s):  
W.J. de Ruijter ◽  
Sharma Renu

Established methods for measurement of lattice spacings and angles of crystalline materials include x-ray diffraction, microdiffraction and HREM imaging. Structural information from HREM images is normally obtained off-line with the traveling table microscope or by the optical diffractogram technique. We present a new method for precise measurement of lattice vectors from HREM images using an on-line computer connected to the electron microscope. It has already been established that an image of crystalline material can be represented by a finite number of sinusoids. The amplitude and the phase of these sinusoids are affected by the microscope transfer characteristics, which are strongly influenced by the settings of defocus, astigmatism and beam alignment. However, the frequency of each sinusoid is solely a function of overall magnification and periodicities present in the specimen. After proper calibration of the overall magnification, lattice vectors can be measured unambiguously from HREM images.Measurement of lattice vectors is a statistical parameter estimation problem which is similar to amplitude, phase and frequency estimation of sinusoids in 1-dimensional signals as encountered, for example, in radar, sonar and telecommunications. It is important to properly model the observations, the systematic errors and the non-systematic errors. The observations are modelled as a sum of (2-dimensional) sinusoids. In the present study the components of the frequency vector of the sinusoids are the only parameters of interest. Non-systematic errors in recorded electron images are described as white Gaussian noise. The most important systematic error is geometric distortion. Lattice vectors are measured using a two step procedure. First a coarse search is obtained using a Fast Fourier Transform on an image section of interest. Prior to Fourier transformation the image section is multiplied with a window, which gradually falls off to zero at the edges. The user indicates interactively the periodicities of interest by selecting spots in the digital diffractogram. A fine search for each selected frequency is implemented using a bilinear interpolation, which is dependent on the window function. It is possible to refine the estimation even further using a non-linear least squares estimation. The first two steps provide the proper starting values for the numerical minimization (e.g. Gauss-Newton). This third step increases the precision with 30% to the highest theoretically attainable (Cramer and Rao Lower Bound). In the present studies we use a Gatan 622 TV camera attached to the JEM 4000EX electron microscope. Image analysis is implemented on a Micro VAX II computer equipped with a powerful array processor and real time image processing hardware. The typical precision, as defined by the standard deviation of the distribution of measurement errors, is found to be <0.003Å measured on single crystal silicon and <0.02Å measured on small (10-30Å) specimen areas. These values are ×10 times larger than predicted by theory. Furthermore, the measured precision is observed to be independent on signal-to-noise ratio (determined by the number of averaged TV frames). Obviously, the precision is restricted by geometric distortion mainly caused by the TV camera. For this reason, we are replacing the Gatan 622 TV camera with a modern high-grade CCD-based camera system. Such a system not only has negligible geometric distortion, but also high dynamic range (>10,000) and high resolution (1024x1024 pixels). The geometric distortion of the projector lenses can be measured, and corrected through re-sampling of the digitized image.


2020 ◽  
pp. 66-72
Author(s):  
Irina A. Piterskikh ◽  
Svetlana V. Vikhrova ◽  
Nina G. Kovaleva ◽  
Tatyana O. Barynskaya

Certified reference materials (CRM) composed of propyl (11383-2019) and isopropyl (11384-2019) alcohols solutions were created for validation of measurement procedures and control of measurement errors of measurement results of mass concentrations of toxic substances (alcohol) in biological objects (urine, blood) and water. Two ways of establishing the value of the certified characteristic – mass consentration of propanol-1 or propanol-2 have been studied. The results obtained by the preparation procedure and comparison with the standard are the same within the margin of error.


2019 ◽  
Vol 7 (2A) ◽  
Author(s):  
Camilo Fuentes Serrano ◽  
Juan Reinaldo Estevez Alvares ◽  
Alfredo Montero Alvarez ◽  
Ivan Pupo Gonzales ◽  
Zahily Herrero Fernandez ◽  
...  

A method for determination of Cr, Fe, Co, Ni, Cu, Zn, Hg and Pb in waters by Energy Dispersive X Ray Fluorescence (EDXRF) was implemented, using a radioisotopic source of 238Pu. For previous concentration was employed a procedure including a coprecipitation step with ammonium pyrrolidinedithiocarbamate (APDC) as quelant agent, the separation of the phases by filtration, the measurement of filter by EDXRF and quantification by a thin layer absolute method. Sensitivity curves for K and L lines were obtained respectively. The sensitivity for most elements was greater by an order of magnitude in the case of measurement with a source of 238Pu instead of 109Cd, which means a considerable decrease in measurement times. The influence of the concentration in the precipitation efficiency was evaluated for each element. In all cases the recoveries are close to 100%, for this reason it can be affirmed that the method of determination of the studied elements is quantitative. Metrological parameters of the method such as trueness, precision, detection limit and uncertainty were calculated. A procedure to calculate the uncertainty of the method was elaborated; the most significant source of uncertainty for the thin layer EDXRF method is associated with the determination of instrumental sensitivities. The error associated with the determination, expressed as expanded uncertainty (in %), varied from 15.4% for low element concentrations (2.5-5 μg/L) to 5.4% for the higher concentration range (20-25 μg/L).


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