Impact of the control-command process in a photovoltaic conversion chain on the power line channel transfer function in the narrowband PLC frequency range

2017 ◽  
Vol 2017 (1) ◽  
pp. 719-723
Author(s):  
Christopher Wawrzyniak ◽  
Véronique Moeyaert ◽  
François Vallee
Author(s):  
Joachim Frank

Cryo-electron microscopy combined with single-particle reconstruction techniques has allowed us to form a three-dimensional image of the Escherichia coli ribosome.In the interior, we observe strong density variations which may be attributed to the difference in scattering density between ribosomal RNA (rRNA) and protein. This identification can only be tentative, and lacks quantitation at this stage, because of the nature of image formation by bright field phase contrast. Apart from limiting the resolution, the contrast transfer function acts as a high-pass filter which produces edge enhancement effects that can explain at least part of the observed variations. As a step toward a more quantitative analysis, it is necessary to correct the transfer function in the low-spatial-frequency range. Unfortunately, it is in that range where Fourier components unrelated to elastic bright-field imaging are found, and a Wiener-filter type restoration would lead to incorrect results. Depending upon the thickness of the ice layer, a varying contribution to the Fourier components in the low-spatial-frequency range originates from an “inelastic dark field” image. The only prospect to obtain quantitatively interpretable images (i.e., which would allow discrimination between rRNA and protein by application of a density threshold set to the average RNA scattering density may therefore lie in the use of energy-filtering microscopes.


1998 ◽  
Vol 274 (1) ◽  
pp. H358-H365 ◽  
Author(s):  
Takayuki Sato ◽  
Toru Kawada ◽  
Toshiaki Shishido ◽  
Hiroshi Miyano ◽  
Masashi Inagaki ◽  
...  

We developed a new method for isolating in situ baroreceptor regions of the rabbit aortic depressor nerve (ADN) and estimated the transfer function from pressure to afferent nerve activity in the frequency range of 0.01–5 Hz by a white noise technique. Complete isolation of the baroreceptor area of the right ADN was made in situ by ligation of the innominate artery and the right subclavian and common carotid arteries. We altered the pressure in the isolated baroreceptor area according to a binary quasi-white noise between 80 and 100 mmHg in 12 urethan-anesthetized rabbits. The gain increased two to three times as the frequency of pressure perturbation increased from 0.01 to 2 Hz and then decreased at higher frequencies. The phase slightly led below 0.2 Hz. The squared coherence value was >0.8 in the frequency range of 0.01–4 Hz. The step responses estimated from the transfer function were indistinguishable from those actually observed. We conclude that the baroreceptor transduction of the ADN is governed by linear dynamics under the physiological operating pressure range.


1991 ◽  
Vol 34 (2) ◽  
pp. 427-438 ◽  
Author(s):  
Gerald A. Studebaker ◽  
Robert L. Sherbecoe

Frequency-importance and transfer functions for the Technisonic Studios’ recordings of the CID W-22 word test are reported. These functions may be used to calculate Articulation Index (Al) values or to predict scores on the W-22 test. The functions were derived from the word recognition scores of 8 normal-hearing listeners who were tested under 308 conditions of filtering and masking. The importance function for the W-22 test has a broader frequency range and a different shape than the importance function used in the current ANSI standard on the Articulation Index (ANSI, 1969). The transfer function is similar in slope to to the ANSI transfer function for 256 PB-words, but is shifted to the right of that function by 0.05 Al.


2011 ◽  
Vol 403-408 ◽  
pp. 895-899
Author(s):  
Amit Jain ◽  
B.V. Babu

A frequency dependent approach to defining a dynamic relative gain array (DRGA) is discussed. The approach assumes the availability of a dynamic transfer function based process model for control loop pairing analysis. Two examples are considered: one in which the traditional RGA (based on steady-state gain matrix) gives the correct pairing recommendation and the other in which the traditional RGA suggests wrong pairings particularly in the frequency range of interest. The calculations pertaining to analysis of control loop pairing is performed using MATLAB (version 7.0.1). An inaccurate indication of the amount of interaction present is discussed. The first example uses 2x2 transfer function model [1] and the second one uses 3x3 transfer function model [2].


2012 ◽  
Vol 27 (3) ◽  
pp. 1081-1089 ◽  
Author(s):  
Pascal Pagani ◽  
Amr Ismail ◽  
Ahmed Zeddam

2009 ◽  
Vol 296 (5) ◽  
pp. R1598-R1605 ◽  
Author(s):  
David A. Low ◽  
Jonathan E. Wingo ◽  
David M. Keller ◽  
Scott L. Davis ◽  
Jian Cui ◽  
...  

This study tested the hypothesis that passive heating impairs cerebral autoregulation. Transfer function analyses of resting arterial blood pressure and middle cerebral artery blood velocity (MCA Vmean), as well as MCA Vmean and blood pressure responses to rapid deflation of previously inflated thigh cuffs, were examined in nine healthy subjects under normothermic and passive heat stress (increase core temperature 1.1 ± 0.2°C, P < 0.001) conditions. Passive heating reduced MCA Vmean [change (Δ) of 8 ± 8 cm/s, P = 0.01], while blood pressure was maintained (Δ −1 ± 4 mmHg, P = 0.36). Coherence was decreased in the very-low-frequency range during heat stress (0.57 ± 0.13 to 0.26 ± 0.10, P = 0.001), but was >0.5 and similar between normothermia and heat stress in the low- (0.07–0.20 Hz, P = 0.40) and high-frequency (0.20–0.35 Hz, P = 0.12) ranges. Transfer gain was reduced during heat stress in the very-low-frequency (0.88 ± 0.38 to 0.59 ± 0.19 cm·s−1·mmHg−1, P = 0.02) range, but was unaffected in the low- and high-frequency ranges. The magnitude of the decrease in blood pressure (normothermia: 20 ± 4 mmHg, heat stress: 19 ± 6 mmHg, P = 0.88) and MCA Vmean (13 ± 4 to 12 ± 6 cm/s, P = 0.59) in response to cuff deflation was not affected by the thermal condition. Similarly, the rate of regulation of cerebrovascular conductance (CBVC) after cuff release (0.44 ± 0.22 to 0.38 ± 0.13 ΔCBVC units/s, P = 0.16) and the time for MCA Vmean to recover to precuff deflation baseline (10.0 ± 7.9 to 8.7 ± 4.9 s, P = 0.77) were not affected by heat stress. Counter to the proposed hypothesis, similar rate of regulation responses suggests that heat stress does not impair the ability to control cerebral perfusion after a rapid reduction in perfusion pressure, while reduced transfer function gain and coherence in the very-low-frequency range during heat stress suggest that dynamic cerebral autoregulation is improved during spontaneous oscillations in blood pressure within this frequency range.


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