A major event of nervous system development is the migration of granule cell neurones, during the early postnatal development of the cerebellar cortex, from their germinating zone in the external granular layer to their final location in the internal granular layer. During migration, many granule cells are seen in direct cell-surface contact with processes of Bergmann glia, a subclass of astrocytes. In the neurological mutant mouse weaver, however, migration of granule cells is impaired, probably due to a deficit in cell-cell interactions. To gain insight into the cellular and molecular mechanisms involved in granule cell migration, we have used a modification of an in vitro assay system, previously described by Moonen et al., which displays migratory behaviour in small tissue explants during several days of suspension culture. The aim of this study was to investigate the process of granule cell migration by using antibodies directed against cell-surface components of developing neural cells. We report here that migration of 3H-thymidine-labelled granule cell neurones can be modified by Fab fragments of both mono- and polyclonal L1 antibodies, but not by Fab fragments of polyclonal antibodies prepared against mouse liver membranes, which also react with cerebellar cell surfaces.

Spin torque from spin current applied to a nanoscale region of a ferromagnet can act as negative magnetic damping and thereby excite self-oscillations of its magnetization. In contrast, spin torque uniformly applied to the magnetization of an extended ferromagnetic film does not generate self-oscillatory magnetic dynamics but leads to reduction of the saturation magnetization. Here we report studies of the effect of spin torque on a system of intermediate dimensionality-a ferromagnetic nanowire. We observe coherent self-oscillations of magnetization in a ferromagnetic nanowire serving as the active region of a spin torque oscillator driven by spin orbit torques. Our work demonstrates that magnetization selfoscillations can be excited in a one-dimensional magnetic system and that dimensions of the active region of spin torque oscillators can be extended beyond the nanometre length scale.

The use of spin waves as information carriers in spintronic devices can substantially reduce energy losses by eliminating the ohmic heating associated with electron transport. Yet, the excitation of short-wavelength spin waves in nanoscale magnetic systems remains a significant challenge. Here, we propose a method for their coherent generation in a heterostructure composed of antiferromagnetically coupled magnetic layers. The driven dynamics of naturally formed nanosized stacked pairs of magnetic vortex cores is used to achieve this aim. The resulting spin-wave propagation is directly imaged by time-resolved scanning transmission X-ray microscopy. We show that the dipole-exchange spin waves excited in this system have a linear, non-reciprocal dispersion and that their wavelength can be tuned by changing the driving frequency.

The magnetic relaxation processes following the dynamical excitation of the spin system of ferromagnets are investigated by ferromagnetic resonance ͑FMR͒ between 1 and 70 GHz using epitaxial Fe 3 Si films as a prototype system. Two relaxation channels, i.e., dissipative, isotropic Gilbert damping G as well as anisotropic two-magnon scattering ⌫, are simultaneously identified by frequency and angle dependent FMR and quantitatively analyzed. The scattering rates due to two-magnon scattering at crystallographic defects for spin waves propagating in ͗100͘ and ͗110͘ directions, ␥⌫ ͗100͘ = 0.25͑2͒ GHz and ␥⌫ ͗110͘ = 0.04͑2͒ GHz, and the Gilbert damping term G = 0.051͑1͒ GHz are determined. We show that changing the film thickness from 8 to 40 nm and slightly modifying the Fe concentration influence the relaxation channels. Our results, which reveal the contributions of longitudinal and transverse relaxation processes may be of general importance for the understanding of spin-wave dynamics in magnetic structures.

Ferromagnetism in certain alloys consisting of magnetic and nonmagnetic species can be activated by the presence of chemical disorder. This phenomenon is linked to an increase in the number of nearest-neighbor magnetic atoms and local variations in the electronic band structure due to the existence of disorder sites. An approach to induce disorder is through exposure of the chemically ordered alloy to energetic ions; collision cascades formed by the ions knock atoms from their ordered sites and the concomitant vacancies are filled randomly via thermal diffusion of atoms at room temperature. The ordered structure thereby undergoes a transition into a metastable solid solution. Here we demonstrate the patterning of highly resolved magnetic structures by taking advantage of the large increase in the saturation magnetization of Fe60Al40 alloy triggered by subtle atomic displacements. The sigmoidal characteristic and sensitive dependence of the induced magnetization on the atomic displacements manifests a sub-50 nm patterning resolution. Patterning of magnetic regions in the form of stripes separated by ∼ 40 nm wide spacers was performed, wherein the magnet/spacer/magnet structure exhibits reprogrammable parallel (↑/spacer/↑) and antiparallel (↑/spacer/↓) magnetization configurations in zero field. Materials in which the magnetic behavior can be tuned via ion-induced phase transitions may allow the fabrication of novel spin-transport and memory devices using existing lateral patterning tools.

X-ray absorption and magnetic circular dichroism spectra at both the Fe and Pt L(3,2) edges were measured on wet-chemically synthesized monodisperse Fe(50)Pt(50) particles with a mean diameter of 6.3 nm before and after complete removal of the organic ligands and the oxide shell covering the particles by soft hydrogen plasma resulting in a pure metallic state. After thermal treatment of the metallic particles, the coercive field increased by a factor of 6, the orbital magnetic moment at the Fe site increased by 330% and is reduced at the Pt site by 30%, while the effective spin moments did not change. A decrease of the frequency of oscillations in the extended x-ray absorption fine structure at the Pt L(3,2) edges provides evidence for crystallographic changes towards the L1(0) phase.

Spin waves offer intriguing novel perspectives for computing and signal processing, since their damping can be lower than the Ohmic losses in conventional CMOS circuits. For controlling the spatial extent and propagation of spin waves on the actual chip, magnetic domain walls show considerable potential as magnonic waveguides. However, low-loss guidance of spin waves with nanoscale wavelengths, in particular around angled tracks, remains to be shown. Here we experimentally demonstrate that such advanced control of propagating spin waves can be obtained using natural features of magnetic order in an interlayer exchange-coupled, anisotropic ferromagnetic bilayer. Using Scanning Transmission X-Ray Microscopy, we image generation of spin waves and their propagation across distances exceeding multiple times the wavelength, in extended planar geometries as well as along one-dimensional domain walls, which can be straight and curved. The observed range of wavelengths is between 1 µm and 150 nm, at corresponding excitation frequencies from 250 MHz to 3 GHz. Our results show routes towards practical implementation of magnonic waveguides employing domain walls in future spin wave logic and computational circuits.

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