Possibility to realize spin-orbit-induced correlated physics in iridium fluorides

Recent theoretical predictions of "unprecedented proximity" of the electronic ground state of iridium fluorides to the SU(2) symmetric $j_{\mathrm{eff}}=1/2$ limit, relevant for superconductivity in iridates, motivated us to investigate their crystal and electronic structure. To this aim, we performed high-resolution x-ray powder diffraction, Ir L$_3$-edge resonant inelastic x-ray scattering, and quantum chemical calculations on Rb$_2$[IrF$_6$] and other iridium fluorides. Our results are consistent with the Mott insulating scenario predicted by Birol and Haule [Phys. Rev. Lett. 114, 096403 (2015)], but we observe a sizable deviation of the $j_{\mathrm{eff}}=1/2$ state from the SU(2) symmetric limit. Interactions beyond the first coordination shell of iridium are negligible, hence the iridium fluorides do not show any magnetic ordering down to at least 20 K. A larger spin-orbit coupling in iridium fluorides compared to oxides is ascribed to a reduction of the degree of covalency, with consequences on the possibility to realize spin-orbit-induced strongly correlated physics in iridium fluorides

A method of eta' decay product selection to study partial chiral symmetry restoration

In case of chiral U_A(1) symmetry restoration the mass of the eta' boson (the ninth, would-be Goldstone boson) is decreased, thus its production cross section is heavily enhanced. The eta' decays (through one of its decay channels) into five pions. These pions will not be correlated in terms of Bose-Einsten correlations, thus the production enhancement changes the strength of two-pion correlation functions at low momentum. Preliminary results strongly support the mass decrease of the eta' boson. In this paper we propose a method to select pions coming from eta' decays. We investigate the efficiency of the proposed kinematical cut in several collision systems and energies with several simulators. We prove that our method can be used in all investigeted collision systems.Comment: Talk at the VI Workshop on Particle Correlations and Femtoscopy, Kiev, September 14-18, 2010. 6 pages, 3 figures. This work was supported by the OTKA grant NK73143 and M. Csanad's Bolyai scholarshi

Reaction-Diffusion System in a Vesicle with Semi-Permeable Membrane

We study the Schloegl model in a vesicle with semi-permeable membrane. The diffusion constant takes a smaller value in the membrane region, which prevents the outflow of self-catalytic product. A nonequilibrium state is stably maintained inside of the vesicle. Nutrients are absorbed and waste materials are exhausted through the membrane by diffusion. It is interpreted as a model of primitive metabolism in a cell.Comment: 8 pages, 6 figure

Escherichia coli MazF Leads to the Simultaneous Selective Synthesis of Both “Death Proteins” and “Survival Proteins”

The Escherichia coli mazEF module is one of the most thoroughly studied toxin–antitoxin systems. mazF encodes a stable toxin, MazF, and mazE encodes a labile antitoxin, MazE, which prevents the lethal effect of MazF. MazF is an endoribonuclease that leads to the inhibition of protein synthesis by cleaving mRNAs at ACA sequences. Here, using 2D-gels, we show that in E. coli, although MazF induction leads to the inhibition of the synthesis of most proteins, the synthesis of an exclusive group of proteins, mostly smaller than about 20 kDa, is still permitted. We identified some of those small proteins by mass spectrometry. By deleting the genes encoding those proteins from the E. coli chromosome, we showed that they were required for the death of most of the cellular population. Under the same experimental conditions, which induce mazEF-mediated cell death, other such proteins were found to be required for the survival of a small sub-population of cells. Thus, MazF appears to be a regulator that induces downstream pathways leading to death of most of the population and the continued survival of a small sub-population, which will likely become the nucleus of a new population when growth conditions become less stressful

A Hydrolase of Trehalose Dimycolate Induces Nutrient Influx and Stress Sensitivity to Balance Intracellular Growth of Mycobacterium tuberculosis

SummaryChronic tuberculosis in an immunocompetent host is a consequence of the delicately balanced growth of Mycobacterium tuberculosis (Mtb) in the face of host defense mechanisms. We identify an Mtb enzyme (TdmhMtb) that hydrolyzes the mycobacterial glycolipid trehalose dimycolate and plays a critical role in balancing the intracellular growth of the pathogen. TdmhMtb is induced under nutrient-limiting conditions and remodels the Mtb envelope to increase nutrient influx but concomitantly sensitizes Mtb to stresses encountered in the host. Consistent with this, a ΔtdmhMtb mutant is more resilient to stress and grows to levels higher than those of wild-type in immunocompetent mice. By contrast, mutant growth is retarded in MyD88−/− mice, indicating that TdmhMtb provides a growth advantage to intracellular Mtb in an immunocompromised host. Thus, the effects and countereffects of TdmhMtb play an important role in balancing intracellular growth of Mtb in a manner that is directly responsive to host innate immunity

Galeorhinus galeus, Tope

Tope (Galeorhinus galeus) is a medium-sized (to 200 cm total length) bentho-pelagic shark, widespread in temperate waters in most oceans. It is present across the Northeast, Eastern Central, Southwest, and Southeast Atlantic, the Mediterranean Sea, the Eastern Indian, and across all of the Pacific, except in the Northwest Pacific. It occurs on continental shelves and upper to mid slopes from shallow inshore to well offshore to depths of 826 m, though most frequently to depths of 200 m. Genetic and tagging data support up to six separate subpopulations of Tope and while the species makes extensive movements within each of the subpopulations, there is no evidence of mixing between them. Tope has a particularly low biological productivity with a late age-at-maturity and triennial reproductive cycle. It is caught globally as target and bycatch in industrial and small-scale demersal and pelagic gillnet and longline fisheries, and to a lesser extent in trawl and hook-and-line fisheries. Tope is often retained for the meat and fins but is discarded or released in some areas, in line with regional management measures. Steep subpopulation and stock reductions of >80% over the past three generation lengths (79 years) have occurred in the Southwest Atlantic, southern Africa, and Australia. In the Northeast Atlantic, the subpopulation is estimated to have undergone a reduction of 76% over the past three generation lengths (79 years). The New Zealand stock is estimated to have undergone a reduction of 30?49% over the past three generation lengths (79 years). In the Northeast Pacific, a dramatic decline in the subpopulation occurred in the early 1940s, with no recovery until 1997?2004 when localized management led to a localized increase in abundance. The consistent steep subpopulation reductions across most of the analyzed subpopulations and stocks together with the lack of movement between the subpopulations are cause for serious concern. Management in Australia, probably aided by the immigration of large mature animals from New Zealand, appears to have stabilized that stock since 2000. The subpopulation in the Northeast Atlantic has been stable in recent years, possibly due to management measures, and there is some recovery in part of the Northeast Pacific. Release of this species is mandatory since 2011 off Canada. Release is mandatory in European Union waters for line-caught Tope. The global population is estimated to have undergone a reduction of 88% with the highest probability of >80% reduction over the last three generations (79 years) due to levels of exploitation, and Tope is assessed as Critically Endangered A2bd.Fil: Walker, T. I.. University of Melbourne; AustraliaFil: Rigby, C. L.. James Cook University; AustraliaFil: Pacoureau, N.. University Fraser Simon; CanadáFil: Ellis, J.. No especifíca;Fil: Kulka, D. W.. No especifíca;Fil: Chiaramonte, Gustavo Enrique. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Parque Centenario. Museo Argentino de Ciencias Naturales "Bernardino Rivadavia"; ArgentinaFil: Herman, K.. Georgia Aquarium; Estados Unido

Morphological and pathological response in primary systemic therapy of patients with breast cancer and the prediction of disease free survival

AIM: To identify breast cancer subtypes likely to respond to primary systemic therapy (PST or neoadjuvant therapy) and to assess the accuracy of physical examination (PE) and breast ultrasonography (US) in evaluating and predicting residual size of breast carcinoma following PST. METHODS: 116 patients who received at least two cycles of PST between 1998 and 2009 were selected from a prospectively collected clinical database. Radiological assessment was done by mammography and US. Prior to PST, tumors were subclassified according to core biopsy (NCB) and/or fine-needle aspiration-based immunohistochemical profiles of NCB. Pathological response rates were assessed following the surgeries by using Chevallier classification. Tumor measurements by PE and US were obtained before and after PST. Different clinical measurements were compared with histological findings. Disease-free survival (DFS) was assessed. RESULTS: Pathological complete remission (pCR=Chevallier I/II) was observed in 25 patients (21.5%), 44% of whom had triple negative histology, 28% Her2 positive and 76% had high-grade tumor. Of 116 patients, 24 received taxane-based PST, 48 combined taxane + anthracycline treatment, 8 trastuzumab combinations, 21 anthracycline-based treatments, and 15 other treatments. In the taxane treated group, the pCR rate was 30%, in the taxane + anthracycline group 25%, in the anthracycline group 9.5%, and in trastuzumab group 37.5%. After PST, PE and US were both significantly associated with pathology (P<0.001 and P=0.004, respectively). Concerning OS, significant difference was observed between the Chevallier III and IV group (P=0.031) in favor of Chevallier III group. In the pCR group, fewer events were observed during the follow-up period. CONCLUSIONS: Our results show that even limited, routinely used immunohistochemical profiling of tumors can predict the likelihood of pCR to PST: patients with triple negative and Her2-positive cancers are more likely to achieve pCR to PST. Also, PE is better correlated with pathological findings than US