82 research outputs found
Two-Fermion Bound States within the Bethe-Salpeter Approach
To solve the spinor-spinor Bethe-Salpeter equation in Euclidean space we
propose a novel method related to the use of hyperspherical harmonics. We
suggest an appropriate extension to form a new basis of spin-angular harmonics
that is suitable for a representation of the vertex functions. We present a
numerical algorithm to solve the Bethe-Salpeter equation and investigate in
detail the properties of the solution for the scalar, pseudoscalar and vector
meson exchange kernels including the stability of bound states. We also compare
our results to the non relativistic ones and to the results given by light
front dynamics.Comment: 32 pages, XIII Tables, 8 figure
Identifying Archaeological Bone via Non-Destructive ZooMS and the Materiality of Symbolic Expression: Examples from Iroquoian Bone Points.
Today, practical, functional and symbolic choices inform the selection of raw materials for worked objects. In cases where we can discern the origin of worked bone, tooth, ivory and antler objects in the past, we assume that similar choices are being made. However, morphological species identification of worked objects is often impossible due to the loss of identifying characteristics during manufacture. Here, we describe a novel non-destructive ZooMS (Zooarchaeology by Mass Spectrometry) method which was applied to bone points from Pre-Contact St. Lawrence Iroquoian village sites in southern Quebec, Canada. The traditional ZooMS technique requires destructive analysis of a sample, which can be problematic when dealing with artefacts. Here we instead extracted proteins from the plastic bags in which the points had been stored. ZooMS analysis revealed hitherto unexpected species, notably black bear (Ursus americanus) and human (Homo sapiens sapiens), used in point manufacture. These surprising results (confirmed through genomic sequencing) highlight the importance of advancing biomolecular research in artefact studies. Furthermore, they unexpectedly and exceptionally allow us to identify and explore the tangible, material traces of the symbolic relationship between bears and humans, central to past and present Iroquoian cosmology and mythology
Results and Limits of Time Division Multiplexing for the BICEP Array High Frequency Receivers
Time-Division Multiplexing is the readout architecture of choice for many
ground and space experiments, as it is a very mature technology with proven
outstanding low-frequency noise stability, which represents a central challenge
in multiplexing. Once fully populated, each of the two BICEP Array high
frequency receivers, observing at 150GHz and 220/270GHz, will have 7776 TES
detectors tiled on the focal plane. The constraints set by these two receivers
required a redesign of the warm readout electronics. The new version of the
standard Multi Channel Electronics, developed and built at the University of
British Columbia, is presented here for the first time. BICEP Array operates
Time Division Multiplexing readout technology to the limits of its capabilities
in terms of multiplexing rate, noise and crosstalk, and applies them in
rigorously demanding scientific application requiring extreme noise performance
and systematic error control. Future experiments like CMB-S4 plan to use TES
bolometers with Time Division/SQUID-based readout for an even larger number of
detectors.Comment: 10 pages, 7 figures, Submitted to Journal of Low Temperature Physic
Berry Flesh and Skin Ripening Features in Vitis vinifera as Assessed by Transcriptional Profiling
Background
Ripening of fleshy fruit is a complex developmental process involving the differentiation of tissues with separate functions. During grapevine berry ripening important processes contributing to table and wine grape quality take place, some of them flesh- or skin-specific. In this study, transcriptional profiles throughout flesh and skin ripening were followed during two different seasons in a table grape cultivar âMuscat Hamburgâ to determine tissue-specific as well as common developmental programs.
Methodology/Principal Findings
Using an updated GrapeGen Affymetrix GeneChipÂź annotation based on grapevine 12Ăv1 gene predictions, 2188 differentially accumulated transcripts between flesh and skin and 2839 transcripts differentially accumulated throughout ripening in the same manner in both tissues were identified. Transcriptional profiles were dominated by changes at the beginning of veraison which affect both pericarp tissues, although frequently delayed or with lower intensity in the skin than in the flesh. Functional enrichment analysis identified the decay on biosynthetic processes, photosynthesis and transport as a major part of the program delayed in the skin. In addition, a higher number of functional categories, including several related to macromolecule transport and phenylpropanoid and lipid biosynthesis, were over-represented in transcripts accumulated to higher levels in the skin. Functional enrichment also indicated auxin, gibberellins and bHLH transcription factors to take part in the regulation of pre-veraison processes in the pericarp, whereas WRKY and C2H2 family transcription factors seems to more specifically participate in the regulation of skin and flesh ripening, respectively.
Conclusions/Significance
A transcriptomic analysis indicates that a large part of the ripening program is shared by both pericarp tissues despite some components are delayed in the skin. In addition, important tissue differences are present from early stages prior to the ripening onset including tissue-specific regulators. Altogether, these findings provide key elements to understand berry ripening and its differential regulation in flesh and skin.This study was financially supported by GrapeGen Project funded by Genoma España within a collaborative agreement with Genome Canada. The authors also thank The Ministerio de Ciencia e Innovacion for project BIO2008-03892 and a bilateral collaborative grant with Argentina (AR2009-0021). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.Peer reviewe
- âŠ