Scalar O(N) Model at Finite Temperature -- 2PI Effective Potential in Different Approximations

We calculate the two-particle irreducible (2PI) effective potential of the O(N) linear sigma model in 1+1 dimensions. The approximations we use are the next-to-leading order of a 1/N expansion (for arbitrary N) and a kind of "resummed loop approximation" for N=1. We show that the effective potential of the 1/N expansion is convex for N=4 and N=10 whereas it is not for the "loop" expansion and the case N=1 of the 1/N expansion.Comment: LaTeX, 5 pages. Contribution to the Proceedings of 6th Conference on Strong and Electroweak Matter 2004 (SEWM04), Helsinki, Finland, 16-19 Jun 200

The 2PI finite temperature effective potential of the O(N) linear sigma model in 1+1 dimensions, at next-to-leading order in 1/N

We study the O(N) linear sigma model in 1+1 dimensions. We use the 2PI formalism of Cornwall, Jackiw and Tomboulis in order to evaluate the effective potential at finite temperature. At next-to-leading order in a 1/N expansion one has to include the sums over "necklace" and generalized "sunset" diagrams. We find that - in contrast to the Hartree approximation - there is no spontaneous symmetry breaking in this approximation, as to be expected for the exact theory. The effective potential becomes convex throughout for all parameter sets which include N=4,10,100, couplings lambda=0.1 and 0.5, and temperatures between 0.2 and 1. The Green's functions obtained by solving the Schwinger-Dyson equations are enhanced in the infrared region. We also compare the effective potential as function of the external field phi with those obtained in various other approximations.Comment: 19 pages, 9 figures; v2: references added, some changes in the tex

General Motors Company: Restructured to Rediscover American Innovation

Many analysts predicted that General Motors was not salvageable. However, after a government-backed restructuring, the company seems to be doing much better. The big question is whether the turnaround is sustainable. The company is investing heavily in technology in an effort to continue its record of success. This case examines GM up to its reorganization and also details its current strategies

Isolation by Elevation: Genetic Structure at Neutral and Putatively Non-Neutral Loci in a Dominant Tree of Subtropical Forests, Castanopsis eyrei

The distribution of genetic diversity among plant populations growing along elevational gradients can be affected by neutral as well as selective processes. Molecular markers used to study these patterns usually target neutral processes only, but may also be affected by selection. In this study, the effects of elevation and successional stage on genetic diversity of a dominant tree species were investigated controlling for neutrality of the microsatellite loci used. = 0.15). Population differentiation followed a model of isolation by distance but additionally, strongly significant isolation by elevation was found, both for neutral loci and the putatively selected locus.. The study underlines the importance to check the selective neutrality of marker loci in analyses of population structure

RNA-Seq analysis of soft rush (Juncus effusus): transcriptome sequencing, de novo assembly, annotation, and polymorphism identification

Background: Juncus effusus L. (family: Juncaceae; order: Poales) is a helophytic rush growing in temperate damp or wet terrestrial habitats and is of almost cosmopolitan distribution. The species has been studied intensively with respect to its interaction with co-occurring plants as well as microbes being involved in major biogeochemical cycles. J. effusus has biotechnological value as component of Constructed Wetlands where the plant has been employed in phytoremediation of contaminated water. Its genome has not been sequenced. Results: In this study we carried out functional annotation and polymorphism analysis of de novo assembled RNA-Seq data from 18 genotypes using 249 million paired-end Illumina HiSeq reads and 2.8 million 454 Titanium reads. The assembly comprised 158,591 contigs with a mean contig length of 780bp. The assembly was annotated using the dammit! annotation pipeline, which queries the databases OrthoDB, Pfam-A, Rfam, and runs BUSCO (Benchmarking Single-Copy Ortholog genes). In total, 111,567 contigs (70.3%) were annotated with functional descriptions, assigned gene ontology terms, and conserved protein domains, which resulted in 30,932 non-redundant gene sequences. Results of BUSCO and KEGG pathway analyses were similar for J. effusus as for the well-studied members of the Poales, Oryza sativa and Sorghum bicolor. A total of 566,433 polymorphisms were identified in transcribed regions with an average frequency of 1 polymorphism in every 171 bases. Conclusions: The transcriptome assembly was of high quality and genome coverage was sufficient for global analyses. This annotated knowledge resource can be utilized for future gene expression analysis, genomic feature comparisons, genotyping, primer design, and functional genomics in J. effusus.German Academic Exchange Program (DAAD); German Science Foundation (DFG) [MI 1500/2-1]Open access journalThis item from the UA Faculty Publications collection is made available by the University of Arizona with support from the University of Arizona Libraries. If you have questions, please contact us at [email protected]

Regionally Altered Immunosignals of Surfactant Protein-G, Vascular and Non-Vascular Elements of the Neurovascular Unit after Experimental Focal Cerebral Ischemia in Mice, Rats, and Sheep

The surfactant protein-G (SP-G) has recently been discovered in the brain and linked to fluid balance regulations. Stroke is characterized by impaired vessel integrity, promoting water influx and edema formation. The neurovascular unit concept (NVU) has been generated to cover not only ischemic affections of neurons or vessels but also other regionally associated cells. This study provides the first spatio-temporal characterization of SP-G and NVU elements after experimental stroke. Immunofluorescence labeling was applied to explore SP-G, vascular and cellular markers in mice (4, 24, and 72 h of ischemia), rats (24 h of ischemia), and sheep (two weeks of ischemia). Extravasated albumin indicated vascular damage within ischemic areas. Quantifications revealed decreasing SP-G signals in the ischemia-affected neocortex and subcortex. Inverse immunosignals of SP-G and vascular elements existed throughout all models. Despite local associations between SP-G and the vasculature, a definite co-localization was not seen. Along with a decreased SP- G-immunoreactivity in ischemic areas, signals originating from neurons, glial elements, and the extracellular matrix exhibited morphological alterations or changed intensities. Collectively, this study revealed regional alterations of SP-G, vascular, and non-vascular NVU elements after ischemia, and may thus stimulate the discussion about the role of SP-G during stroke