A Singly Terminated Frequency Function with Three Parameters

Nature ◽  
1962 ◽  
Vol 195 (4843) ◽  
pp. 770-772 ◽  
Author(s):  
R. ASH ◽  
E. O. POWELL
Keyword(s):  
2016 ◽  
Vol 2 (1) ◽  
Author(s):  
Lila San Roque

AbstractDespite their central role in question formation, content interrogatives in spontaneous conversation remain relatively under-explored cross-linguistically. This paper outlines the structure of ‘where’ expressions in Duna, a language spoken in Papua New Guinea, and examines where-questions in a small Duna data set in terms of their frequency, function, and the responses they elicit. Questions that ask ‘where?’ have been identified as a useful tool in studying the language of space and place, and, in the Duna case and elsewhere, show high frequency and functional flexibility. Although where-questions formulate place as an information gap, they are not always answered through direct reference to canonical places. While some question types may be especially “socially costly” (Levinson 2012), asking ‘where’ perhaps provides a relatively innocuous way of bringing a particular event or situation into focus.


1988 ◽  
Vol 255 (2) ◽  
pp. H375-H385 ◽  
Author(s):  
M. Miniati ◽  
J. C. Parker ◽  
M. Pistolesi ◽  
J. T. Cartledge ◽  
D. J. Martin ◽  
...  

The reabsorption of albumin from the pleural space was measured in eight dogs receiving 0.5 ml intrapleural injection of 131I-labeled albumin and a simultaneous intravenous injection of 125I-labeled albumin. Plasma curves for both tracers were obtained over 24 h. The 125I-albumin curve served as input function of albumin for interstitial spaces, including pleura, whereas the 131I-albumin curve represented the output function from pleural space. The frequency function of albumin transit times from pleural space to plasma was obtained by deconvolution of input-output plasma curves. Plasma recovery of 131I-albumin was complete by 24 h, and the mean transit time from pleura to plasma averaged 7.95 +/- 1.57 (SD) h. Albumin reabsorption occurred mainly via lymphatics as indicated by experiments in 16 additional dogs in which their right lymph ducts or thoracic ducts were ligated before intrapleural injection. A pleural lymph flow of 0.020 +/- 0.003 (SD) ml.kg-1.h-1 was estimated, which is balanced by a comparable filtration of fluid into the pleural space. This suggests that, under physiological conditions, the subpleural lymphatics represent an important control mechanism of pleural liquid pressure.


1961 ◽  
Vol 14 (4) ◽  
pp. 598 ◽  
Author(s):  
EJ Williams

Though randomly moving insects released from a central point in a uniform environment are often found to be distributed according to a circular normal distribution, their larvae will not conform to this distribution. When such insects lay at a constant rate and are subject to constant mortality, their larvae are found to be spatially distributed according to a highly peaked frequency function, depending on the modified Bessel function of the second kind. This theoretical conclusion is in good agreement with published data. Some of the properties of the theoretical distribution are discussed.


1957 ◽  
Vol 24 (3) ◽  
pp. 435-439
Author(s):  
S. Mahalingam

Abstract A one-term approximate solution is given for the amplitudes of steady forced vibration of a single-degree-of-freedom system with a nonlinear (nonsymmetrical) spring characteristic. The method is similar to that of Martienssen (1), but the construction uses a modified curve (or “frequency function”) in place of the actual spring characteristic, the curve being so chosen that it gives the correct frequency for free vibrations. The method is extended to deal with a nonlinear vibration absorber fitted to a linear system.


Author(s):  
Sebastian Alphonse ◽  
Geoffrey A. Williamson

AbstractSignal design is an important component for good performance of radar systems. Here, the problem of determining a good radar signal with the objective of minimizing autocorrelation sidelobes is addressed, and the first comprehensive comparison of a range of signals proposed in the literature is conducted. The search is restricted to a set of nonlinear, frequency-modulated signals whose frequency function is monotonically nondecreasing and antisymmetric about the temporal midpoint. This set includes many signals designed for smaller sidelobes including our proposed odd polynomial frequency signal (OPFS) model and antisymmetric time exponentiated frequency modulated (ATEFM) signal model. The signal design is optimized based on autocorrelation sidelobe levels with constraints on the autocorrelation mainlobe width and leakage of energy outside the allowed bandwidth, and we compare our optimized design with the best signal found from parameterized signal model classes in the literature. The quality of the overall best such signal is assessed through comparison to performance of a large number of randomly generated signals from within the search space. From this analysis, it is found that the OPFS model proposed in this paper outperforms all other contenders for most combinations of the objective functions and is expected to be better than nearly all signals within the entire search set.


1977 ◽  
Vol 48 (11) ◽  
pp. 1500-1502
Author(s):  
John H. Myers ◽  
Charles F. Frost

2019 ◽  
Vol 09 (04) ◽  
pp. 2150002
Author(s):  
Mario Kieburg

Recently, subclasses of polynomial ensembles for additive and multiplicative matrix convolutions were identified which were called Pólya ensembles (or polynomial ensembles of derivative type). Those ensembles are closed under the respective convolutions and, thus, build a semi-group when adding by hand a unit element. They even have a semi-group action on the polynomial ensembles. Moreover, in several works transformations of the bi-orthogonal functions and kernels of a given polynomial ensemble were derived when performing an additive or multiplicative matrix convolution with particular Pólya ensembles. For the multiplicative matrix convolution on the complex square matrices the transformations were even done for general Pólya ensembles. In the present work, we generalize these results to the additive convolution on Hermitian matrices, on Hermitian anti-symmetric matrices, on Hermitian anti-self-dual matrices and on rectangular complex matrices. For this purpose, we derive the bi-orthogonal functions and the corresponding kernel for a general Pólya ensemble which was not done before. With the help of these results, we find transformation formulas for the convolution with a fixed matrix or a random matrix drawn from a general polynomial ensemble. As an example, we consider Pólya ensembles with an associated weight which is a Pólya frequency function of infinite order. But we also explicitly evaluate the Gaussian unitary ensemble as well as the complex Laguerre (aka Wishart, Ginibre or chiral Gaussian unitary) ensemble. All results hold for finite matrix dimension. Furthermore, we derive a recursive relation between Toeplitz determinants which appears as a by-product of our results.


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