Simulation of waviness in neutron guides

As the trend of neutron guide designs points towards longer and more complex guides, imperfections such as waviness becomes increasingly important. Simulations of guide waviness has so far been limited by a lack of reasonable waviness models. We here present a stochastic description of waviness and its implementation in the McStas simulation package. The effect of this new implementation is compared to the guide simulations without waviness and the simple, yet unphysical, waviness model implemented in McStas 1.12c and 2.0

Effects of ground movements on realistic guide models for the European Spallation Source

We model the effect of ground movement, based on empirical experience, on the transport properties of long neutron guides by ray-tracing simulations. Our results reproduce the large losses found by an earlier study for a simple model, while for a more realistic engineering model of guide mounting, we find the losses to be significantly smaller than earlier predicted. A detailed study of the guide for the cold neutron spectrometer BIFROST at the European Spallation Source shows that the loss is 7.0(5) % for wavelengths of 2.3-4.0 {\AA}; the typical operational wavelength range of the instrument. This amount of loss does not call for mitigation by overillumination as suggested in the previous work. Our work serves to quantify the robustness of the transport properties of long neutron guides, in construction or planning at neutron facilities worldwide.Comment: 8 pages, 12 figure

CAMEA: Guide Report

This document describes the best current candidate for a CAMEA guide made by the optimizer guide bot. The guide bot tool generates the McStas instrument and iFit files necessary for guide optimization, making it easy to investigate a large number of possibilities. The baseline requirements for the CAMEA guide is a 15 mm x 15 mm sample 0.6 m from the end of the guide, with a divergence requirement of ±0.75 degrees in the horizontal direction and ±1.0 degrees in the vertical direction. The distance between moderator and sample is 170 m. The guide does provide flux in a larger area than the requirement and at larger divergences, but the phase space illumination is only uniform within the requirement. The guide is intended to be used for the wavelength range 1.65 \AA to 6.4 \AA, but was optimized for a wavelength range of 1.0 \AA to 3.6 \AA, because experience with the optimizer shows that the results are better when optimizing for a slightly lower wavelength range than needed

Gut bacteria and necrotizing enterocolitis: cause or effect?

Development of necrotising enterocolitis (NEC) is considered to be dependent on the bacterial colonisation of the gut. With little concordance between published data and a recent study failing to detect a common strain in infants with NEC, more questions than answers are arising about our understanding of this complex disease

Haematological and biochemical reference intervals for free-ranging brown bears (Ursus arctos) in Sweden

Background: Establishment of haematological and biochemical reference intervals is important to assess health of animals on individual and population level. Reference intervals for 13 haematological and 34 biochemical variables were established based on 88 apparently healthy free-ranging brown bears (39 males and 49 females) in Sweden. The animals were chemically immobilised by darting from a helicopter with a combination of medetomidine, tiletamine and zolazepam in April and May 2006-2012 in the county of Dalarna, Sweden. Venous blood samples were collected during anaesthesia for radio collaring and marking for ecological studies. For each of the variables, the reference interval was described based on the 95% confidence interval, and differences due to host characteristics sex and age were included if detected. To our knowledge, this is the first report of reference intervals for free-ranging brown bears in Sweden.Results: The following variables were not affected by host characteristics: red blood cell, white blood cell, monocyte and platelet count, alanine transaminase, amylase, bilirubin, free fatty acids, glucose, calcium, chloride, potassium, and cortisol. Age differences were seen for the majority of the haematological variables, whereas sex influenced only mean corpuscular haemoglobin concentration, aspartate aminotransferase, lipase, lactate dehydrogenase, beta-globulin, bile acids, triglycerides and sodium.Conclusions: The biochemical and haematological reference intervals provided and the differences due to host factors age and gender can be useful for evaluation of health status in free-ranging European brown bears

Further evidence of Chelonid herpesvirus 5 (ChHV5) latency : High levels of ChHV5 DNA detected in clinically healthy marine turtles

The Chelonid herpesvirus 5 (ChHV5) has been consistently associated with fibropapillomatosis (FP), a transmissible neoplastic disease of marine turtles. Whether ChHV5 plays a causal role remains debated, partly because while FP tumours have been clearly documented to contain high concentrations of ChHV5 DNA, recent PCRbased studies have demonstrated that large proportions of asymptomatic marine turtles are also carriers of ChHV5. We used a real-time PCR assay to quantify the levels of ChHV5 Glycoprotein B (gB) DNA in both tumour and non-tumour skin tissues, from clinically affected and healthy turtles drawn from distant ocean basins across four species. In agreement with previous studies, higher ratios of viral to host DNA were consistently observed in tumour versus non-tumour tissues in turtles with FP. Unexpectedly however, the levels of ChHV5 gB DNA in clinically healthy turtles were significantly higher than in non-tumour tissues from FP positive turtles. Thus, a large proportion of clinically healthy sea turtle populations worldwide across species carry ChHV5 gB DNA presumably through persistent latent infections. ChHV5 appears to be ubiquitous regardless of the animals' clinical conditions. Hence, these results support the theory that ChHV5 is a near ubiquitous virus with latency characteristics requiring co-factors, possibly environmental or immune related, to induce FP