The Cone Algebra and a Kernel Characterization of Green Operators

Author(s):  
J. Seiler
2003 ◽  
Vol 80 (3) ◽  
pp. 274-280 ◽  
Author(s):  
Jesper Pram Nielsen ◽  
Dorthe Kjær Pedersen ◽  
Lars Munck

Fuel ◽  
2017 ◽  
Vol 190 ◽  
pp. 318-327 ◽  
Author(s):  
Rajesh Kumar Prasad ◽  
Siddhant Jain ◽  
Gaurav Verma ◽  
Avinash Kumar Agarwal

Author(s):  
Zafar Iqbal ◽  
Imran Pasha ◽  
Muhammad Abrar ◽  
Muhammad Shakeel Hanif ◽  
Sharoon Mashi

1977 ◽  
Vol 70 (2) ◽  
pp. 243-265 ◽  
Author(s):  
H I Krausz ◽  
W O Friesen

In order to characterize synaptic transmission at a unitary facilitating synapse in the lobster cardiac ganglion, a new nonlinear systems analysis technique for discrete-input systems was developed and applied. From the output of the postsynaptic cell in response to randomly occurring presynaptic nerve impulses, a set of kernels, analogous to Wiener kernels, was computed. The kernels up to third order served to characterize, with reasonable accuracy, the input-output properties of the synapse. A mathematical model of the synapse was also tested with a random impulse train and model predictions were compared with experimental synaptic output. Although the model proved to be even more accurate overall than the kernel characterization, there were slight but consistent errors in the model's performance. These were also reflected as differences between model and experimental kernels. It is concluded that a random train analysis provides a comprehensive and objective comparison between model and experiment and automatically provides an arbitrarily accurate characterization of a system's input-output behavior, even in complicated cases where other approaches are impractical.


2014 ◽  
Vol 8 (3-4) ◽  
pp. 379-390 ◽  
Author(s):  
Clément Aubry ◽  
Rozenn Desmare ◽  
Luc Jaulin

Author(s):  
B. L. Soloff ◽  
T. A. Rado

Mycobacteriophage R1 was originally isolated from a lysogenic culture of M. butyricum. The virus was propagated on a leucine-requiring derivative of M. smegmatis, 607 leu−, isolated by nitrosoguanidine mutagenesis of typestrain ATCC 607. Growth was accomplished in a minimal medium containing glycerol and glucose as carbon source and enriched by the addition of 80 μg/ ml L-leucine. Bacteria in early logarithmic growth phase were infected with virus at a multiplicity of 5, and incubated with aeration for 8 hours. The partially lysed suspension was diluted 1:10 in growth medium and incubated for a further 8 hours. This permitted stationary phase cells to re-enter logarithmic growth and resulted in complete lysis of the culture.


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