2,434 research outputs found
How adaptation currents change threshold, gain and variability of neuronal spiking
Many types of neurons exhibit spike rate adaptation, mediated by intrinsic
slow -currents, which effectively inhibit neuronal responses. How
these adaptation currents change the relationship between in-vivo like
fluctuating synaptic input, spike rate output and the spike train statistics,
however, is not well understood. In this computational study we show that an
adaptation current which primarily depends on the subthreshold membrane voltage
changes the neuronal input-output relationship (I-O curve) subtractively,
thereby increasing the response threshold. A spike-dependent adaptation current
alters the I-O curve divisively, thus reducing the response gain. Both types of
adaptation currents naturally increase the mean inter-spike interval (ISI), but
they can affect ISI variability in opposite ways. A subthreshold current always
causes an increase of variability while a spike-triggered current decreases
high variability caused by fluctuation-dominated inputs and increases low
variability when the average input is large. The effects on I-O curves match
those caused by synaptic inhibition in networks with asynchronous irregular
activity, for which we find subtractive and divisive changes caused by external
and recurrent inhibition, respectively. Synaptic inhibition, however, always
increases the ISI variability. We analytically derive expressions for the I-O
curve and ISI variability, which demonstrate the robustness of our results.
Furthermore, we show how the biophysical parameters of slow
-conductances contribute to the two different types of adaptation
currents and find that -activated -currents are
effectively captured by a simple spike-dependent description, while
muscarine-sensitive or -activated -currents show a
dominant subthreshold component.Comment: 20 pages, 8 figures; Journal of Neurophysiology (in press
Classification and Redshift Estimation in Multi-Color Surveys
We present a photometric method for identifying stars, galaxies and quasars
in multi-color surveys and estimating multi-color redshifts for the
extragalactic objects. We use a library of >65000 color templates for
comparison with observed objects. The method was originally developed for the
Calar Alto Deep Imaging Survey (CADIS), but is now used in a variety of survey
projects. We checked its performance by spectroscopy of CADIS objects, where it
provides high reliability (6 mistakes among 151 objects with R<24), especially
for the quasar selection, and redshifts accurate within sigma_z = 0.03 for
galaxies and sigma_z = 0.1 for quasars. For an optimization of future surveys,
a few model surveys are compared, which use the same amount of telescope time
but different filter sets. In summary, medium-band surveys perform superior to
broad-band surveys although they collect less photons. A full account of this
work is already in print.Comment: 7 pages, 2 figures, proceedings of MPA/ESO/MPE Joint Astronomy
Conference Mining THE SKY held in Garching, Germany, July 31 - Aug 4, 200
5G Positioning and Mapping with Diffuse Multipath
5G mmWave communication is useful for positioning due to the geometric
connection between the propagation channel and the propagation environment.
Channel estimation methods can exploit the resulting sparsity to estimate
parameters(delay and angles) of each propagation path, which in turn can be
exploited for positioning and mapping. When paths exhibit significant spread in
either angle or delay, these methods breakdown or lead to significant biases.
We present a novel tensor-based method for channel estimation that allows
estimation of mmWave channel parameters in a non-parametric form. The method is
able to accurately estimate the channel, even in the absence of a specular
component. This in turn enables positioning and mapping using only diffuse
multipath. Simulation results are provided to demonstrate the efficacy of the
proposed approach
The Energy Landscape of Myoglobin: An Optical Study
In this paper we demonstrate how the potential energy surface of a protein, which determines its conformational degrees of freedom, can be constructed from a series of advanced nonlinear optical experiments. The energy landscape of myoglobin was probed by studying its low-temperature structural dynamics, using several spectral hole burning and photon echo techniques. The spectral diffusion of the heme group of the protein was studied on a time scale ranging from nanoseconds to several days while covering a temperature range from 100 mK to 23 K. The spectral line broadening, as measured in three-pulse stimulated photon echo experiments, occurs in a stepwise fashion, while the exact time dependence of the line width is critically dependent on temperature. From these results we obtained the energy barriers between the conformational states of the protein. Aging time dependent hole-burning experiments show that, at 100 mK, it takes several days for the protein to reach thermal equilibrium. When, after this period a spectral hole is burned, the line broadening induced by well-defined temperature cycles is partly reversed over a period of several hours. From this we conclude that a rough structure is superimposed on the overall shape of the potential energy surface of the protein. By combining the hole burning and photon echo results, we construct a detailed image of this energy landscape, supporting the general concept of a structural hierarchy. More specifically, we show that the number of conformational substates in the lower hierarchical tiers is much lower than was previously anticipated and, in fact, is comparable to the number of taxonomic substates.
How adaptation currents and synaptic inhibition change threshold, gain and variability of neuronal spiking : From Twenty Second Annual Computational Neuroscience Meeting: CNS*2013 Paris, France. 13-18 July 2013
Published by BioMed Central
Ladenbauer, Josef ; Augustin, Moritz ; Obermayer, Klaus : How adaptation currents and synaptic inhibition change threshold, gain and variability of neuronal spiking. - In: BMC Neuroscience. - ISSN 1471-2202 (online). - 14 (2013), suppl. 1, P299. - doi:10.1186/1471-2202-14-S1-P299
- …