Session:management of drainage near source – disconnection/minimise surface water entering public drainage

Many combined sewer networks are currently constrained due to lack of capacity. Surface water entering the network may have an impact on the local environment by causing additional spills from Combined Sewer Overflows (CSOs) and flooding events. With the increasing number of developments taking place in Scotland, more and more demands are being placed upon the existing wastewater assets and infrastructure of the drainage utility, Scottish Water. The principal way of preventing these CSO spills/flooding event s is to reduce the number of surface water connections to the combined sewer network and promote more surface water discharges to nearby watercourses.The problem is being addressed by examining all development applications as they are considered by a drainage planning officer in the water authority. The research reported in this paper is investigating the conditions under which it is reasonable and practical for Scottish Water to accept surface water flows into its combined sewer network . This paper presents a summary of the initial findings of the research to date by examining a sample of the sites examined. The objective of the work is to develop a methodology to support a rigorous stance on the acceptance of surface water flows into the combined sewer network. The results have not as yet been obtained

Spin flip from dark to bright states in InP quantum dots

We report measurements of the time for spin flip from dark (non-light emitting) exciton states in quantum dots to bright (light emitting) exciton states in InP quantum dots. Dark excitons are created by two-photon excitation by an ultrafast laser. The time for spin flip between dark and bright states is found to be approximately 200 ps, independent of density and temperature below 70 K. This is much shorter than observed in other quantum dot systems. The rate of decay of the luminescence intensity, approximately 300 ps, is not simply equal to the radiative decay rate from the bright states, because the rate of decay is limited by the rate of conversion from dark excitons into bright excitons. The dependence of the luminescence decay time on the spin flip time is a general effect that applies to many experiments.Comment: 3 figure

Siege of Gerona [Material cartográfico]

A la part inferior de la làmina: William Blagkood & soons, Edinburgh & LondonMapa gravat, representades les bateries de l'exèrcit frencès en color blau. Xarxa de camins, arbres i conreus. Ombrejat del relleuCopia digital. Madrid : Ministerio de Cultura. Subdirección General de Coordinación Bibliotecaria, 200

Sequential emergence and clinical implications of viral mutants with K70E and K65R mutation in reverse transcriptase during prolonged tenofovir monotherapy in rhesus macaques with chronic RT-SHIV infection.

BackgroundWe reported previously on the emergence and clinical implications of simian immunodeficiency virus (SIVmac251) mutants with a K65R mutation in reverse transcriptase (RT), and the role of CD8+ cell-mediated immune responses in suppressing viremia during tenofovir therapy. Because of significant sequence differences between SIV and HIV-1 RT that affect drug susceptibilities and mutational patterns, it is unclear to what extent findings with SIV can be extrapolated to HIV-1 RT. Accordingly, to model HIV-1 RT responses, 12 macaques were inoculated with RT-SHIV, a chimeric SIV containing HIV-1 RT, and started on prolonged tenofovir therapy 5 months later.ResultsThe early virologic response to tenofovir correlated with baseline viral RNA levels and expression of the MHC class I allele Mamu-A*01. For all animals, sensitive real-time PCR assays detected the transient emergence of K70E RT mutants within 4 weeks of therapy, which were then replaced by K65R mutants within 12 weeks of therapy. For most animals, the occurrence of these mutations preceded a partial rebound of plasma viremia to levels that remained on average 10-fold below baseline values. One animal eventually suppressed K65R viremia to undetectable levels for more than 4 years; sequential experiments using CD8+ cell depletion and tenofovir interruption demonstrated that both CD8+ cells and continued tenofovir therapy were required for sustained suppression of viremia.ConclusionThis is the first evidence that tenofovir therapy can select directly for K70E viral mutants in vivo. The observations on the clinical implications of the K65R RT-SHIV mutants were consistent with those of SIVmac251, and suggest that for persons infected with K65R HIV-1 both immune-mediated and drug-dependent antiviral activities play a role in controlling viremia. These findings suggest also that even in the presence of K65R virus, continuation of tenofovir treatment as part of HAART may be beneficial, particularly when assisted by antiviral immune responses

Identification of glyceraldehyde‐3‐phosphate dehydrogenase as a Ca2+‐dependent fusogen in human neutrophil cytosol

The membrane fusion events observed during neutrophil degranulation are important aspects of the immunoregulatory system. In an attempt to understand the regulation of granule‐plasma membrane fusion, we have begun characterizing human neutrophil cytosol for fusion activity, finding that 50% of the fusogenic activity could be attributed to members of the annexin family of proteins. The major non‐annexin fusion activity (25% of the total cytosolic activity) was enriched by ion exchange chromatography after depletion of annexins by Ca2+‐dependent phospholipid affinity chromatography. The fusion activity co‐purified with a 10,14‐kDa dimer identified as leukocyte L1 (which was non‐fusogenic), along with an approximately 36‐kDa protein. This protein was identified as glyceraldehyde‐3‐phosphate dehydrogenase (GAPDH) by amino‐terminal sequencing, and the fusion activity was verified using commercially available GAPDH. GAPDH may play an important role in degranulation because it is as potent as annexin I on a mass basis and may constitute up to 25% of the total cytosolic fusion activity of the neutrophil. J. Leukoc. Biol. 63: 331–336; 1998.Peer Reviewedhttps://deepblue.lib.umich.edu/bitstream/2027.42/142089/1/jlb0331.pd

Exercise rehabilitation following intensive care unit discharge for recovery from critical illness:executive summary of a Cochrane Collaboration systematic review

Skeletal muscle wasting and weakness are major complications of critical illness and underlie the profound physical and func-\ud tional impairments experienced by survivors after discharge from the intensive care unit (ICU). Exercise-based rehabilitation\ud has been shown to be bene\ud fi\ud cial when delivered during ICU admission. This review aimed to determine the effectiveness of\ud exercise rehabilitation initiated after ICU discharge on primary outcomes of functional exercise capacity and health-related\ud quality of life. We sought randomized controlled trials, quasi-randomized controlled trials, and controlled clinical trials compar-\ud ing an exercise intervention commenced after ICU discharge vs. any other intervention or a control or\ud ‘\ud usual care\ud ’\ud programme\ud in adult survivors of critical illness. Cochrane Central Register of Controlled Trials, Medical Literature Analysis and Retrieval Sys-\ud tem Online (MEDLINE), Excerpta Medica Database, and Cumulative Index to Nursing and Allied Health Literature databases\ud were searched up to February 2015. Dual, independent screening of results, data extraction, and quality appraisal were per-\ud formed. We included six trials involving 483 patients. Overall quality of evidence for both outcomes was very low. All studies\ud evaluated functional exercise capacity, with three reporting positive effects in favour of the intervention. Only two studies\ud evaluated health-related quality of life and neither reported differences between intervention and control groups. Meta-\ud analyses of data were precluded due to variation in study design, types of interventions, and selection and reporting of out-\ud come measurements. We were unable to determine an overall effect on functional exercise capacity or health-related quality\ud of life of interventions initiated after ICU discharge for survivors of critical illness. Findings from ongoing studies are awaited.\ud Future studies need to address methodological aspects of study design and conduct to enhance rigour, quality, and synthesis