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1.
Phys Rev Lett ; 123(22): 225101, 2019 Nov 29.
Artigo em Inglês | MEDLINE | ID: mdl-31868399

RESUMO

Aided by fully kinetic simulations, spacecraft observations of magnetic reconnection in Earth's magnetotail are analyzed. The structure of the electron diffusion region is in quantitative agreement with the numerical model. Of special interest, the spacecraft data reveal how reconnection is mediated by off-diagonal stress in the electron pressure tensor breaking the frozen-in law of the electron fluid.

2.
Phys Rev Lett ; 120(5): 055101, 2018 Feb 02.
Artigo em Inglês | MEDLINE | ID: mdl-29481157

RESUMO

Fully kinetic simulations of asymmetric magnetic reconnection reveal the presence of magnetic-field-aligned beams of electrons flowing toward the topological magnetic x line. Within the ∼6d_{e} electron-diffusion region, the beams become oblique to the local magnetic field, providing a unique signature of the electron-diffusion region where the electron frozen-in law is broken. The numerical predictions are confirmed by in situ Magnetospheric Multiscale spacecraft observations during asymmetric reconnection at Earth's dayside magnetopause.

3.
Phys Rev Lett ; 117(18): 185101, 2016 Oct 28.
Artigo em Inglês | MEDLINE | ID: mdl-27835028

RESUMO

Supported by a kinetic simulation, we derive an exclusion energy parameter E_{X} providing a lower kinetic energy bound for an electron to cross from one inflow region to the other during magnetic reconnection. As by a Maxwell demon, only high-energy electrons are permitted to cross the inner reconnection region, setting the electron distribution function observed along the low-density side separatrix during asymmetric reconnection. The analytic model accounts for the two distinct flavors of crescent-shaped electron distributions observed by spacecraft in a thin boundary layer along the low-density separatrix.

4.
Biotech Histochem ; 73(3): 164-73, 1998 May.
Artigo em Inglês | MEDLINE | ID: mdl-9674887

RESUMO

In sensory systems, insight into synaptic arrangements on cells of known physiological response properties has helped our understanding of the structural basis for these properties. To carry out these types of studies, however, synaptic types in the region of interest must be defined. Unfortunately, defining synaptic types in the brainstem has proved to be a challenging enterprise. Our study was done to classify synapses in the gustatory part of the nucleus solitarius using objective quantitative criteria and a cluster analysis procedure. Cluster analysis allows classification of a population of objects, such as synaptic terminals, into groups that exhibit similar characteristics. Six terminal types were identified using cluster analysis and subsequent analyses of variance and post hoc tests. Unlike classification schemes used for the cerebral cortex, where synaptic apposition density thickness and shape of vesicles is useful (Gray's Type I and II synapses), the concentration of vesicles in a terminal was a more useful measurement with which to classify terminals in the nucleus solitarius. To validate that vesicle density (vesicles/microm2) is a useful defining characteristic to classify terminals in the nucleus solitarius, terminals of a known type were used. GABAergic terminals were identified using postembedding immunohistochemical techniques, and their vesicle density was determined. GABAergic terminals fall into the range of two of the terminal types defined by the cluster analysis and, based on vesicle density, two types of GABAergic terminals were identified. We conclude that vesicle density is a helpful means to identify synapses in this brainstem nucleus.


Assuntos
Neurônios Aferentes/classificação , Terminações Pré-Sinápticas/classificação , Núcleo Solitário/fisiologia , Núcleo Solitário/ultraestrutura , Paladar/fisiologia , Análise de Variância , Animais , Análise por Conglomerados , Coloide de Ouro , Imuno-Histoquímica , Masculino , Neurônios Aferentes/fisiologia , Neurônios Aferentes/ultraestrutura , Ratos , Ratos Sprague-Dawley , Inclusão do Tecido , Ácido gama-Aminobutírico/fisiologia
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