Investigation of thin n-in-p planar pixel modules for the ATLAS upgrade

In view of the High Luminosity upgrade of the Large Hadron Collider (HL-LHC), planned to start around 2023-2025, the ATLAS experiment will undergo a replacement of the Inner Detector. A higher luminosity will imply higher irradiation levels and hence will demand more ra- diation hardness especially in the inner layers of the pixel system. The n-in-p silicon technology is a promising candidate to instrument this region, also thanks to its cost-effectiveness because it only requires a single sided processing in contrast to the n-in-n pixel technology presently employed in the LHC experiments. In addition, thin sensors were found to ensure radiation hardness at high fluences. An overview is given of recent results obtained with not irradiated and irradiated n-in-p planar pixel modules. The focus will be on n-in-p planar pixel sensors with an active thickness of 100 and 150 um recently produced at ADVACAM. To maximize the active area of the sensors, slim and active edges are implemented. The performance of these modules is investigated at beam tests and the results on edge efficiency will be shown

On the Dichotomy between the Nodal and Antinodal Excitations in High-temperature Superconductors

Angle-resolved photoemission data on optimally- and under-doped high temperature superconductors reveal a dichotomy between the nodal and antinodal electronic excitations. In this paper we propose an explanation of this unusual phenomenon by employing the coupling between the quasiparticle and the commensurate/incommensurate magnetic excitations.Comment: 11 pages, 9 figure

Bravo/Nr-CAM Is Closely Related to the Cell Adhesion Molecules L1 and Ng-CAM and Has a Similar Heterodimer Structure

Diverse cell-surface molecules of the nervous system play an important role in specifying cell interactions during development. Using a method designed to generate mAbs against neural surface molecules of defined molecular weight, we have previously reported on the surface protein, Bravo, found in the developing avian retinotectal system. Bravo is immunologically detected on developing optic fibers in the retina, but absent from distal regions of the same fibers in the tectum. We have isolated cDNA clones encompassing the entire coding region of Bravo, including clones containing five alternative sequences of cDNA. These putative alternatively spliced sequences encode stretches of polypeptide ranging in length from 10-93 amino acids and are predicted to be both extra- and intracellular. The deduced primary structure of Bravo reveals that, like the cell adhesion molecules (CAMs) chicken Ng- CAM and mouse L1, Bravo is composed of six Ig-like domains, five fibronectin type III repeats, a transmembrane domain, and a short cytoplasmic region. Recently, the cDNA sequence of a related molecule, Nr-CAM, was reported and its possible identity with Bravo discussed (Grumet, M., V. Mauro, M. P. Burgoon, G. E. Edelman, and B. A. Cunningham. 1991. J. Cell Biol. 113:1399-1412). Here we confirm this identity and moreover show that Bravo is found on Muller glial processes and end-feet in the developing retina. In contrast to the single polypeptide chain structure of Nr-CAM reported previously, we show that Bravo has a heterodimer structure composed of an alpha chain of M(r) 140/130 and a beta chain of 60-80 kD. As with L1 and Ng-CAM, the two chains of Bravo are generated from an intact polypeptide by cleavage at identical locations and conserved sites within all three molecules (Ser-Arg/Lys-Arg). The similar domain composition and heterodimer structure, as well as the 40% amino acid sequence identity of these molecules, defines them as an evolutionarily related subgroup of CAMs. The relationship of Bravo to molecules known to be involved in cell adhesion and process outgrowth, combined with its pattern of expression and numerous potential isoforms, suggests a complex role for this molecule in cell interactions during neural development

Identifying and Classifying, Quantifying and Visualizing Green Infrastructure via Urban Transects in Rome, Italy and Sydney, Australia

Green Infrastructure is increasingly recognised as an approach to deliver a wide-ranging set of ecosystem services in cities and to operationalize concepts of urban resilience through the better delivery of urban planning, water sensitive urban design and a broad diversity of open space types. This paper argues that the first step in the delivery of effective Green Infrastructure planning and hence ecosystem services is the identification, visualisation and calculus of the full spectrum of existing open space types within urban contexts. To test this idea two case study cities – Rome and Sydney – were selected for their differing geographical origins and planning history. In each city an analysis of the urban fabric through a novel transect mapping process revealed a range of Green Infrastructure types including a diversity of open space, public parks and plazas, streetscapes, greenways and terrain vague. This began by analysing and comparing identified land-uses with existing planning rules, strategies and mechanisms within each city. Through this process we found that for each city significant differences were evident between the formally recognised urban open space and a range of potential additional Green Infrastructure candidates were identified. We then considered the potential recognition and activation of these spaces as critical pieces of overlooked Green Infrastructure into the metrics of a sustainable future city. Comparing these two cities against each other also confirmed the richness of Green Infrastructure types globally across both expanding and contracting cities and highlights differences in data precision, land policy, governance, nomenclature and urban conditions. This research posits that in the absence of the holistic and multi-faceted understanding, metrification and the visualisation of the diversity and distribution of green infrastructure in all its forms then progress towards implementation of robust and resilient cities and their urban ecosystem services will be limited

Topologically Restricted Appearance in the Developing Chick Retinotectal System of Bravo, a Neural Surface Protein: Experimental Modulation by Environmental Cues

A novel neural surface protein, Bravo, shows a pattern of topological restriction in the embryonic chick retinotectal system. Bravo is present on the developing optic fibers in the retina; however, retinal axons in the tectum do not display Bravo. The appearance of Bravo in vitro is modulated by environmental cues. Axons growing out from retinal explants on retinal basal lamina, their natural substrate, express Bravo, whereas such axons growing on collagen do not. Retinal explants provide a valuable system to characterize the mechanism of Bravo restriction, as well as the cellular signals controlling it. Bravo was identified with monoclonal antibodies from a collection generated against exposed molecules isolated by using a selective cell surface biotinylation procedure. The NH2-terminal sequence of Bravo shows similarity with L1, a neural surface molecule which is a member of the immunoglobulin superfamily. This possible relationship to L1, together with its restricted appearance, suggests an involvement of Bravo in axonal growth and guidance