We give evidence for the first time of the onset of undriven fast, collisionless magnetic reconnection during the evolution of an initially homogeneous magnetic field advected in a sheared velocity field. We consider the interaction of the solar wind with the magnetospheric plasma at low latitude and show that reconnection takes place in the layer between adjacent vortices generated by the Kelvin-Helmholtz instability. This process generates coherent magnetic structures with a size comparable to the ion inertial scale, much smaller than the system dimensions but much larger than the electron inertial scale. These magnetic structures are further advected in the plasma in a complex pattern but remain stable over a time interval much longer than their formation time. These results can be crucial for the interpretation of satellite data showing coherent magnetic structures in the Earth's magnetosheath or the magnetotail.

Download full-text PDF

Source
http://dx.doi.org/10.1103/PhysRevLett.101.105001DOI Listing

Publication Analysis

Top Keywords

magnetic structures
12
undriven fast
8
coherent magnetic
8
inertial scale
8
magnetic
5
numerical evidence
4
evidence undriven
4
fast reconnection
4
reconnection solar-wind
4
solar-wind interaction
4

Similar Publications

An increasing number of treatment guidelines recommend rapid initiation of antiretroviral therapy (ART) after the diagnosis of human immunodeficiency virus (HIV) infection. However, data on the association between rapid ART initiation and alterations in brain structure and function remain limited in people with HIV (PWH). A cross-sectional analysis was conducted on HIV-positive men who have sex with men (MSM) undergoing ART.

View Article and Find Full Text PDF

Computational microscopy with coherent diffractive imaging and ptychography.

Nature

January 2025

Department of Physics and Astronomy, University of California, Los Angeles, Los Angeles, CA, USA.

Microscopy and crystallography are two essential experimental methodologies for advancing modern science. They complement one another, with microscopy typically relying on lenses to image the local structures of samples, and crystallography using diffraction to determine the global atomic structure of crystals. Over the past two decades, computational microscopy, encompassing coherent diffractive imaging (CDI) and ptychography, has advanced rapidly, unifying microscopy and crystallography to overcome their limitations.

View Article and Find Full Text PDF

Atomically precise nanoclusters can be assembled into ordered superlattices with unique electronic, magnetic, optical and catalytic properties. The co-crystallization of nanoclusters with functional organic molecules provides opportunities to access an even wider range of structures and properties, but can be challenging to control synthetically. Here we introduce a supramolecular approach to direct the assembly of atomically precise silver nanoclusters into a series of nanocluster‒organic ionic co-crystals with tunable structures and properties.

View Article and Find Full Text PDF

Topological design of π electrons in zigzag-edged graphene nanoribbons (ZGNRs) leads to a wealth of magnetic quantum phenomena and exotic quantum phases. Symmetric ZGNRs typically show antiferromagnetically coupled spin-ordered edge states. Eliminating cross-edge magnetic coupling in ZGNRs not only enables the realization of a class of ferromagnetic quantum spin chains, enabling the exploration of quantum spin physics and entanglement of multiple qubits in the one-dimensional limit, but also establishes a long-sought-after carbon-based ferromagnetic transport channel, pivotal for ultimate scaling of GNR-based quantum electronics.

View Article and Find Full Text PDF

The sequence-structure-function relationship of intrinsic ERα disorder.

Nature

January 2025

Case Comprehensive Cancer Center and Department of Nutrition, Case Western Reserve University School of Medicine, Cleveland, OH, USA.

The oestrogen receptor (ER or ERα), a nuclear hormone receptor that drives most breast cancer, is commonly activated by phosphorylation at serine 118 within its intrinsically disordered N-terminal transactivation domain. Although this modification enables oestrogen-independent ER function, its mechanism has remained unclear despite ongoing clinical trials of kinase inhibitors targeting this region. By integration of small-angle X-ray scattering and nuclear magnetic resonance spectroscopy with functional studies, we show that serine 118 phosphorylation triggers an unexpected expansion of the disordered domain and disrupts specific hydrophobic clustering between two aromatic-rich regions.

View Article and Find Full Text PDF

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!