ab-plane resistivity and possible charge stripe ordering in strongly underdoped La2−x_{2-x}Srx_{x}CuO4_{4} single crystals

We have measured the ab-plane resistivity of La$_{2-x}$Sr$_x$CuO$_4$ single crystals with small Sr content (x=0.052 $\div$ 0.075) between 4.2 and 300 K by using the AC Van der Pauw technique. As recently suggested by Ichikawa et al., the deviation from the linearity of the $\rho_{\mathrm{ab}}(T)$ curve starting at a temperature T$_{\mathrm{ch}}$ can be interpreted as due to a progressive slowing down of the fluctuations of pre-formed charge stripes. An electronic transition of the stripes to a more ordered phase could instead be responsible for some very sharp anomalies present in the $\rho_{\mathrm{ab}}(T)$ of superconducting samples just above $T_{\mathrm{c}}$.Comment: M2S-HTSC-VI Conference paper (2 pages, 2 figures), using Elsevier style espcrc2.st

Cu Nuclear Quadrupole Resonance Study of Site-Disorder and Chemical Pressure Effects on Y(Ba1-xSrx)2Cu4O8

We report a zero-field Cu nuclear quadrupole resonance (NQR) study on the effects of nonmagnetic Sr substitution for high-Tc superconductors, Y(Ba1-xSrx)2Cu4O8 (Tc=82-80 K for x=0-0.4), using a spin-echo technique. The site-disordering and chemical pressure effects associated with doping Sr were observed in the broadened, shifted Cu NQR spectra. Nevertheless, the site disorder did not significantly affect the homogeneity of Cu electron spin dynamics, in contrast to the in-plane impurity. The peak shift of Cu NQR spectrum due to Sr was different between the chain- and the plane-Cu sites, more remarkably than those under a hydrostatic physical pressure, suggesting anisotropic or nonuniform local structural strains. The small decrease of Tc due to Sr can be traced back to either a cancellation effect on Tc between the disorder and the pressure, or an anisotropic or nonuniform chemical pressure effect on Tc.Comment: 4 pages, 5 figure

Synaptic dysfunction, memory deficits and hippocampal atrophy due to ablation of mitochondrial fission in adult forebrain neurons

Well-balanced mitochondrial fission and fusion processes are essential for nervous system development. Loss of function of the main mitochondrial fission mediator, dynamin-related protein 1 (Drp1), is lethal early during embryonic development or around birth, but the role of mitochondrial fission in adult neurons remains unclear. Here we show that inducible Drp1 ablation in neurons of the adult mouse forebrain results in progressive, neuronal subtype-specific alterations of mitochondrial morphology in the hippocampus that are marginally responsive to antioxidant treatment. Furthermore, DRP1 loss affects synaptic transmission and memory function. Although these changes culminate in hippocampal atrophy, they are not sufficient to cause neuronal cell death within 10 weeks of genetic Drp1 ablation. Collectively, our in vivo observations clarify the role of mitochondrial fission in neurons, demonstrating that Drp1 ablation in adult forebrain neurons compromises critical neuronal functions without causing overt neurodegeneration