Suppression of backward scattering of Dirac fermions in iron pnictides Ba(Fe1−x_{1-x}Rux_xAs)2_2

We report electronic transport of Dirac cones when Fe is replaced by Ru, which has an isoelectronic electron configuration to Fe, using single crystals of Ba(Fe$_{1-x}$Ru$_x$As)$_2$. The electronic transport of parabolic bands is shown to be suppressed by scattering due to the crystal lattice distortion and the impurity effect of Ru, while that of the Dirac cone is not significantly reduced due to the intrinsic character of Dirac cones. It is clearly shown from magnetoresistance and Hall coefficient measurements that the inverse of average mobility, proportional to cyclotron effective mass, develops as the square root of the carrier number (n) of the Dirac cones. This is the unique character of the Dirac cone linear dispersion relationship. Scattering of Ru on the Dirac cones is discussed in terms of the estimated mean free path using experimental parameters.Comment: 6 pages, 3 figures, To be published in Phys. Rev.

In Vivo Observation of Structural Changes in Neocortical Catecholaminergic Projections in Response to Drugs of Abuse

Catecholaminergic (dopamine and norepinephrine) projections to the cortex play an important role in cognitive functions and dysfunctions including learning, addiction, and mental disorders. While dynamics of glutamatergic synapses have been well studied in such contexts, little is known regarding catecholaminergic projections, owing to lack of robust methods. Here we report a system to monitor catecholaminergic projections in vivo over the timeframes that such events occur. Green fluorescent protein (GFP) expression driven by tyrosine hydroxylase promoter in a transgenic mouse line enabled us to perform two-photon imaging of cortical catecholaminergic projections through a cranial window. Repetitive imaging of the same axons over 24 h revealed the highly dynamic nature of catecholaminergic boutons. Surprisingly, administration of single high dose methamphetamine (MAP) induced a transient increase in bouton volumes. This new method opens avenues for longitudinal in vivo evaluation of structural changes at single release sites of catecholamines in association with physiology and pathology of cortical functions