scholarly journals Statistical analysis of instantaneous frequency scaling factor as derived from optical disdrometer measurements at K/Q bands

Author(s):  
Michael Zemba ◽  
James Nessel ◽  
Jacquelynne Houts ◽  
Lorenzo Luini ◽  
Carlo Riva
2000 ◽  
Vol 36 (16) ◽  
pp. 1424 ◽  
Author(s):  
D. Mertens ◽  
D. Vanhoenacker-Janvier

Geophysics ◽  
1985 ◽  
Vol 50 (1) ◽  
pp. 167-167
Author(s):  
J. G. Saha

In their paper de Voogd and den Rooijen investigated the effects of spectral bandwidths of zero‐phase signals on interface resolution and also the response of a thin layer when the bandwidth is inadequate. They suggested a type of wavelet manipulation in modeling experiments by a simple frequency scaling and a shift [equation (19)] [Formula: see text] where p is the scaling factor and s is the shift along the frequency axis. The increase in spectral bandwidth which results from this transformation was also derived by the authors in equation (20).


2003 ◽  
Vol 16 (1) ◽  
pp. 115-126 ◽  
Author(s):  
Alexandru Isar ◽  
Dorina Isar ◽  
Mirela Bianu

The aim of this paper is to present a statistical analysis of the continuous linear and bilinear time-frequency representations. Such an analysis can be useful for the estimation of different parameters of not stationary signals corrupted by noise, like the instantaneous frequency or the instantaneous bandwidth. The case of discrete time-frequency representations is also considered. Simulations verify the theoretical results obtained.


1989 ◽  
Vol 43 (3) ◽  
pp. 538-542 ◽  
Author(s):  
Françoise Dousseau ◽  
Marie Therrien ◽  
Michel Pézolet

A method is described for the quantitative subtraction of water from the transmission infrared spectra of aqueous solutions of proteins. The 2125-cm−1 association band of water is used as an internal intensity standard, and the scaling factor is determined with the use of a second-order least-squares fit. This method eliminates the user bias encountered with interactive methods and takes into account small baseline variations due to instrument drift. Statistical analysis of the results obtained demonstrates that at 10% w/w protein concentration, the error is of the order of 2% in the region of the amide I and II bands.


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