86 research outputs found
Selective dilution and magnetic properties of La_{0.7}Sr_{0.3}Mn_{1-x}M'_xO_3 (M' = Al, Ti)
The magnetic lattice of mixed-valence Mn ions in LaSrMnO
is selectively diluted by partial substitution of Mn by Al or Ti. The
ferromagnetic transition temperature and the saturation moment decreases with
substitution in both series. The volume fraction of the non-ferromagnetic
phases evolves non-linearly with the substitution concentration and faster than
theoretically expected. By presenting the data in terms of selective dilutions,
the reduction of is found to be scaled by the relative ionic
concentrations and is consistent with a prediction derived from molecular-field
theory.Comment: 6 pages, 5 figures, REVTex4.0. Submitted to PR
Short range ferromagnetism and spin glass state in
Dynamic magnetic properties of are
reported. The system appears to attain local ferromagnetic order at
K. Below this temperature the low field
magnetization becomes history dependent, i.e. the zero field cooled (ZFC) and
field cooled (FC) magnetization deviate from each other and closely logarithmic
relaxation appears at our experimental time scales (0.3- sec). The zero
field cooled magnetization has a maximum at K,
whereas the field cooled magnetization continues to increase, although less
sharply, also below this temperature. Surprisingly, the dynamics of the system
shows non-equilibrium spin glass (SG) features not only below the maximum in
the ZFC magnetization, but also in the temperature region between this maximum
and . The aging and temperature cycling experiments show only
quantitative differences in the dynamic behavior above and below the maximum in
the ZFC-magnetization; similarly, memory effects are observed in both
temperature regions. We attribute the high temperature behavior to the
existence of clusters of short range ferromagnetic order below
; the configuration evolves into a conventional spin glass
state at temperatures below .Comment: REVTeX style; 8 pages, 8 figure
Fragmentation of exotic oxygen isotopes
Abrasion-ablation models and the empirical EPAX parametrization of projectile fragmentation are described. Their cross section predictions are compared to recent data of the fragmentation of secondary beams of neutron-rich, unstable 19,20,21O isotopes at beam energies near 600 MeV/nucleon as well as data for stable 17,18O beams
Statistical Analsysis to Evaluate Heavy Metal Pollution in the Air Obatained by Moss Technique in Hanoi and its Surrounding Region
The aim of this paper was the application of statistical analysis including principal component analysis to evaluate heavy metal pollution obtained by moss technique in the air of Ha Noi and its surrounding areas and to evaluate potential pollution sources. The concentrations of 33 heavy metal elements in 27 samples of Barbula Indica moss in the investigated region collected in December of 2016 in the investigated area have been examined using multivariate statistical analysis. Five factors explaining 80% of the total variance were identified and their potential sources have been discussed
HDAC7 Is a Repressor of Myeloid Genes Whose Downregulation Is Required for Transdifferentiation of Pre-B Cells into Macrophages
B lymphopoiesis is the result of several cell-commitment, lineage-choice, and differentiation processes. Every differentiation step is characterized by the activation of a new, lineage-specific, genetic program and the extinction of the previous one. To date, the central role of specific transcription factors in positively regulating these distinct differentiation processes to acquire a B cell-specific genetic program is well established. However, the existence of specific transcriptional repressors responsible for the silencing of lineage inappropriate genes remains elusive. Here we addressed the molecular mechanism behind repression of non-lymphoid genes in B cells. We report that the histone deacetylase HDAC7 was highly expressed in pre-B cells but dramatically down-regulated during cellular lineage conversion to macrophages. Microarray analysis demonstrated that HDAC7 re-expression interfered with the acquisition of the gene transcriptional program characteristic of macrophages during cell transdifferentiation; the presence of HDAC7 blocked the induction of key genes for macrophage function, such as immune, inflammatory, and defense response, cellular response to infections, positive regulation of cytokines production, and phagocytosis. Moreover, re-introduction of HDAC7 suppressed crucial functions of macrophages, such as the ability to phagocytose bacteria and to respond to endotoxin by expressing major pro-inflammatory cytokines. To gain insight into the molecular mechanisms mediating HDAC7 repression in pre-B cells, we undertook co-immunoprecipitation and chromatin immunoprecipitation experimental approaches. We found that HDAC7 specifically interacted with the transcription factor MEF2C in pre-B cells and was recruited to MEF2 binding sites located at the promoters of genes critical for macrophage function. Thus, in B cells HDAC7 is a transcriptional repressor of undesirable genes. Our findings uncover a novel role for HDAC7 in maintaining the identity of a particular cell type by silencing lineage-inappropriate genes
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