Detection of new states using forward proton tagging at the LHC

This talk summarises the ongoing proposals to upgrade the ATLAS and CMS detectors by the installation of forward silicon detector systems close to the beam line at distances of approximately 220 m and 420 m from the respective Interaction Points. The physics motivation is outlined, with emphasis on detection of Higgs and Supersymmetric states, and some of the aspects of the apparatus and its performance are briefly described.Comment: For ICHEP XXXIV Conference Proceedings. 4 pages. v2 has updated refs and minor corrections. v3 has cosmetic layout change

The virtual photon structure at HERA

An overview is given of the ongoing measurement at HERA of the parton structure of the photon, as a function of its virtuality. Preliminary ZEUS results show disagreement with an NLO QCD calculation.Comment: To appear in Proc. International Conference on the Structure and Interactions of the Photon, Frascati, April 200

Prompt photon, Drell-Yan and Bethe-Heitler processes in hard photoproduction

We present prospects and requirements for the study at HERA of hard photon processes which generate high $p_T$ photons in the final state, and processes which generate Drell-Yan lepton pairs.Comment: 6 pages, 3 embedded figures. To appear in the proceedings of the workshop "Future physics at HERA

Inclusive Jets and alpha_s at HERA

A brief survey is given of recent HERA results in jet production and prompt photon production, together with the evaluation of the QCD coupling constant alpha_s.Comment: To appear in Proc. International Conference on the Structure and Interactions of the Photon, Frascati, April 200

Resonance Contributions to η\eta Photoproduction on Protons Found Using Dispersion Relations and an Isobar Model

The contributions of the resonances $D_{13}(1520)$, $S_{11}(1535)$, $S_{11}(1650)$, $D_{15}(1675)$, $F_{15}(1680)$, $D_{13}(1700)$, $P_{11}(1710)$, $P_{13}(1720)$ to $\gamma p\to \eta p$ are found from the data on cross sections, beam and target asymmetries using two approaches: fixed-t dispersion relations and an isobar model. Utilization of the two approaches and comparison of the results obtained with different parametrizations of the resonance contributions allowed us to make conclusions about the model-dependence of these contributions. We conclude that the results for the contributions of the resonances $D_{13}(1520)$, $S_{11}(1535)$, $F_{15}(1680)$ to corresponding multipole amplitudes are stable. With this the results for $D_{13}(1520)$ and $F_{15}(1680)$, combined with their PDG photoexcitation helicity amplitudes, allowed us to find the branching ratios $Br (D_{13}(1520)\to \eta N)=0.05\pm 0.02$, $Br (F_{15}(1680)\to \eta N)=0.16\pm0.04$ which have significantly better accuracy than the PDG data. The total Breit-Wigner width of the $S_{11}(1535)$ is model-dependent, we have obtained $\Gamma (S_{11}(1520))=142 MeV$ and $195 MeV$ using dispersion relations and the isobar model, respectively. The results for the $S_{11}(1650)$, $D_{15}(1675)$, $P_{11}(1710)$, $P_{13}(1720)$ are model dependent, only the signs and orders of magnitude of their contributions to multipole amplitudes are determined. The results for the $D_{13}(1700)$ are strongly model-dependent.Comment: 26 pages, 6 figure

Functionally dissociating aspects of event memory: the effects of combined perirhinal and postrhinal cortex lesions on object and place memory in the rat.

Reciprocal interactions between the hippocampus and the perirhinal and parahippocampal cortices form core components of a proposed temporal lobe memory system. For this reason, the involvement of the hippocampus in event memory is thought to depend on its connections with these cortical areas. Contrary to these predictions, we found that NMDA-induced lesions of the putative rat homologs of these cortical areas (perirhinal plus postrhinal cortices) did not impair performance on two allocentric spatial tasks highly sensitive to hippocampal dysfunction. Remarkably, for one of the tasks there was evidence of a facilitation of performance. The same cortical lesions did, however, disrupt spontaneous object recognition and object discrimination reversal learning but spared initial acquisition of the discrimination. This pattern of results reveals important dissociations between different aspects of memory within the temporal lobe. Furthermore, it shows that the perirhinal-postrhinal cortex is not a necessary route for spatial information reaching the hippocampus and that object familiarity-novelty detection depends on different neural substrates than do other aspects of event memory

Cognitive enhancing effects of voluntary exercise, caloric restriction and environmental enrichment: A role for adult hippocampal neurogenesis and pattern separation?

Several behavioural interventions, such as physical exercise, dietary restriction, and enriched environments are associated with both improved cognition and increased adult hippocampal neurogenesis. Whether the learning and memory improvements associated with these interventions are causally dependent on the upregulated neurogenesis has not yet been conclusively determined. However, with the accumulating evidence of a role for adult-born hippocampal neurons in spatial pattern separation, it is possible that the improvements in learning and memory result, at least in part, from an improvement in pattern separation. The following review focuses on three major behavioural manipulations associated with cognitive enhancement: voluntary exercise, caloric restriction, and environmental enrichment (including learning), and how increased neurogenesis may contribute to the enhancement by improving pattern separation.The authors would like to acknowledge financial contribution from the following funding sources: the Innovative Medicine Initiative Joint Undertaking under grant agreement no. 115008, of which resources are composed of a European Federation of Pharmaceutical Industries and Associations in-kind contribution and financial contribution from the European Union's Seventh Framework Programme (FP7/2007–2013); The Wellcome Trust/Medical Research Council (089703/Z/09/Z) and the Biotechnology and Biological Sciences Research Council (grant BB/G019002/1). C.A.O. received funding from the European Union’s Seventh Framework Programme for research, technological development and demonstration under grant agreement no 603016. B.A.K. was supported by Gates Cambridge.This is the author accepted manuscript. The final version is available from Elsevier at http://www.sciencedirect.com/science/article/pii/S235215461500087X