Effect of collisional heat transfer in ICRF power modulation experiment on ASDEX upgrade

ICRF (ion cyclotron range of frequencies) heating experiments were performed in D-H plasmas at various H concentrations on ASDEX Upgrade. The rf power was modulated to measure the electron power deposition profile from electron temperature modulation. To minimize the contribution from indirect collisional heating and the effect of radial transport, the rf power was modulated at 50 Hz. However, peaking of electron temperature modulation was still observed around the hydrogen cyclotron resonance indicating collisional heating contribution. Time dependent simulation of the hydrogen distribution function was performed for the discharges, using the full-wave code AORSA (E.F. Jaeger, et al., Phys. Plasmas, Vol. 8, page 1573 (2001)) coupled to the Fokker-Planck code CO1.31) (R.W. Harvey, et al., Proc. IAEA (1992)). In the present experimental conditions, it was found that modulation of the collisional heating was comparable to that of direct wave damping. Impact of radial transport was also analyzed and found to appreciably smear out the modulation profile and reduce the phase delay

Improving IBD diagnosis and monitoring by understanding preanalytical, analytical and biological fecal calprotectin variability

BACKGROUND: The appropriate clinical use of fecal calprotectin (fCal) might be compromised by incomplete harmonization between assays and within- and between-subjects variability. Our aim was to investigate the analytical and biological variability of fCal in order to provide tools for interpreting fCal in the clinical setting. METHODS: Experiments were conducted to investigate the effects of temperature and storage time on fCal. Thirty-nine controls were enrolled to verify biological variability, and a case-control study was conducted on 134 controls and 110 IBD patients to compare the clinical effectiveness of three different fCal assays: ELISA, CLIA and turbidimetry. RESULTS: A 12% decline in fCal levels was observed within 24 h following stool collection irrespective of storage temperature. Samples were unstable following a longer storage time interval at room temperature. Within- and between-subjects fCal biological variability, at 31% and 72% respectively, resulted in a reference change value (RCV) in the region of 100%. fCal sensitivity in distinguishing between controls and IBD patients is satisfactory (68%), and the specificity high (93%) among young (<65 years), but not among older ( 6565 years) subjects (ROC area: 0.584; 95% CI: 0.399-0.769). Among the young, assays have different optimal thresholds (120 \u3bcg/g for ELISA, 50 \u3bcg/g for CLIA and 100 \u3bcg/g for turbidimetry). CONCLUSIONS: We recommend a standardized preanalytical protocol for fCal, avoiding storage at room temperature for more than 24 h. Different cutoffs are recommended for different fCal assays. In monitoring, the difference between two consecutive measurements appears clinically significant when higher than 100%, the fCal biological variability-derived RCV