Strangeness in stellar matter

A protoneutron star is formed immediately after the gravitational collapse of the core of a massive star. At birth, the hot and high density matter in such a star contains a large number of neutrinos trapped during collapse. Trapped neutrinos generally inhibit the presence of exotic matter — hyperons, a kaon condensate, or quarks. However, as the neutrinos diffuse out in about 10–15 s, the threshold for the appearance of strangeness is reduced; hence, the composition and the structure of the star can change significantly. The effect of exotic, negatively-charged, strangeness-bearing components is always to soften the equation of state, and the possibility exists that the star collapses to a black hole at this time. This could explain why no neutron star has yet been seen in the remnant of supernova SN1987A, even though one certainly existed when neutrinos were detected on Feb. 23, 1987. With new generation neutrino detectors it is feasible to test different theoretical scenarios observationally.     

The Higgs boson mass from precision electroweak data

We present a new global fit to precision electroweak data, including new low- and high-energy data and analyzing the radiative corrections arising from the minimal symmetry breaking sectors of the Standard Model (SM) and its supersymmetric extension (MSSM). It is shown that present data favor a Higgs mass of ${cal O}(M_Z)$: $$M_{H}=76 {+ 152 ?op -50}{? GeV}.$$ We confront our analysis with (meta) stability and perturbative bounds on the SM Higgs mass, and the theoretical upper bound on the MSSM Higgs mass. Present data do not discriminate significantly between the SM and MSSM Higgs mass ranges. We comment in passing on the sensitivity of the Higgs mass determination to the values of $←pha (M_Z)$ and ${←pha_s} (M_Z)$.     

Hyperfine interactions of111In→111Cd probe atoms on GaAs (111)B reconstructed surfaces

Hyperfine Interactions - We have used111In→111Cd perturbed-angular-correlation (PAC) spectroscopy to measure hyperfine interactions at surface sites on two molecular-beam-epitaxy-grown GaAs...     

Nanoprobes for intracellular and single cell surface‐enhanced Raman spectroscopy (SERS)

Surface‐enhanced Raman spectroscopy (SERS) is a promising and powerful label free technique for high resolution analysis of single cells. For intracellular analysis, there is a need for SERS‐active nanoprobes that are minimally invasive to cells, do not affect cell viability, and provide reproducible signals. This work reviews the state‐of‐the‐art tools currently available for intracellular SERS. Various types of SERS probes are considered, including colloidal gold and silver nanoparticles, metallized optical fibers, and tip‐enhanced Raman probes. We also discuss recently developed SERS‐active nanopipettes implemented on the basis of pulled glass microcapillaries. Finally, the critical aspects of selecting an optimal SERS nanoprobe for single‐cell analysis depending on a particular application are summarized. Copyright © 2012 John Wiley & Sons, Ltd.     

Hadamard-encoded sub-slice fMRI for reduced signal dropout

T2?-weighted blood oxygen level-dependent functional magnetic resonance imaging is adversely affected by susceptibility-induced field gradients in brain regions adjoining air interfaces that cause image distortion and signal dropout. Reducing slice thickness diminishes signal dropout but is accompanied by reduced signal-to-noise ratio (SNR). This study proposes simultaneous excitation of subslices with total width equal to the desired slice thickness, employing alternating Hadamard-encoded radiofrequency pulses coupled with incoherent addition of the subslices to achieve reduction of through-plane dephasing with minimal SNR loss but at the expense of a reduction in temporal resolution. Using a sensory task and hypercapnic challenge with breathholding (BH), results with two subslices per slice and a twofold reduction in temporal resolution show improved activation relative to a conventional acquisition. Average (eight subjects) T-scores in the BH task increased by 16% (P<.0003), and activation extent increased by 12% (not significant). In frontal brain regions, significant improvements in BH activation extent (11.4%, P<.05) and T-scores (18%, P<.0002) were demonstrated. Higher temporal resolution can be achieved by tradeoff of SNR.     

细胞内蛋白质磁共振

细胞内的环境异常复杂,其中生物大分子的浓度超过300 mg/mL并占据着大约30%的细胞内空间. 然而,直到目前为止大多数的蛋白质研究仍然在细胞外或是甚至非常稀的缓冲液中进行. 细胞内磁共振（In-cell NMR）提供了一个可以直接非损伤地获取细胞内原子水平信息的方法. 虽然In-cell NMR在近10年里有了较大的发展,但是这一技术尚未成熟. 在该篇综述中,作者首先总结制约这一技术发展的因素以及研究中需要注意的事项,最后讨论了未来的发展方向.