Reduction in benefits of total flux expansion on divertor detachment due to parallel flows

The Super-X divertor (SXD) is an alternative divertor configuration leveraging total flux expansion at the outer strike point (OSP). Key features for the attractiveness of the SXD are facilitated detachment access and control, as predicted by the extended 2-point model (2PM). However, parallel flows are not consistently included in the 2PM. In this work, the 2PM is refined to overcome this limitation: the role of total flux expansion on the pressure balance is made explicit, by including the effect of parallel flows. In consequence, the effect of total flux expansion on detachment access and control is weakened, compared to predictions of the 2PM. This new model partially explains discrepancies between the 2PM and experiments performed on TCV, in ohmic L-mode scenarios, where in core density ramps in lower single-null (SN) configuration, the impact of the OSP major radius Rt on the CIII emission front movement in the divertor outer leg - used as a proxy for the plasma temperature - is substantially weaker than 2PM predictions; and in OSP sweeps in lower and upper SN configurations, with a constant core density, the peak parallel particle flux density at the OSP is almost independent of Rt, while the 2PM predicts a linear dependence. Finally, analytical and numerical modelling of parallel flows in the divertor is presented, to support the argument. It is shown that an increase in total flux expansion can favour supersonic flows at the OSP. Parallel flows are also shown to be relevant by analysing SOLPS-ITER simulations of TCV

Analysis of the human monocyte-derived macrophage transcriptome and response to lipopolysaccharide provides new insights into genetic aetiology of inflammatory bowel disease

The FANTOM5 consortium utilised cap analysis of gene expression (CAGE) to provide an unprecedented insight into transcriptional regulation in human cells and tissues. In the current study, we have used CAGE-based transcriptional profiling on an extended dense time course of the response of human monocyte-derived macrophages grown in macrophage colony-stimulating factor (CSF1) to bacterial lipopolysaccharide (LPS). We propose that this system provides a model for the differentiation and adaptation of monocytes entering the intestinal lamina propria. The response to LPS is shown to be a cascade of successive waves of transient gene expression extending over at least 48 hours, with hundreds of positive and negative regulatory loops. Promoter analysis using motif activity response analysis (MARA) identified some of the transcription factors likely to be responsible for the temporal profile of transcriptional activation. Each LPS-inducible locus was associated with multiple inducible enhancers, and in each case, transient eRNA transcription at multiple sites detected by CAGE preceded the appearance of promoter-associated transcripts. LPS-inducible long non-coding RNAs were commonly associated with clusters of inducible enhancers. We used these data to re-examine the hundreds of loci associated with susceptibility to inflammatory bowel disease (IBD) in genome-wide association studies. Loci associated with IBD were strongly and specifically (relative to rheumatoid arthritis and unrelated traits) enriched for promoters that were regulated in monocyte differentiation or activation. Amongst previously-identified IBD susceptibility loci, the vast majority contained at least one promoter that was regulated in CSF1-dependent monocyte-macrophage transitions and/or in response to LPS. On this basis, we concluded that IBD loci are strongly-enriched for monocyte-specific genes, and identified at least 134 additional candidate genes associated with IBD susceptibility from reanalysis of published GWA studies. We propose that dysregulation of monocyte adaptation to the environment of the gastrointestinal mucosa is the key process leading to inflammatory bowel disease

Hydroponic technologies

This open access book, written by world experts in aquaponics and related technologies, provides the authoritative and comprehensive overview of the key aquaculture and hydroponic and other integrated systems, socio-economic and environmental aspects. Aquaponic systems, which combine aquaculture and vegetable food production offer alternative technology solutions for a world that is increasingly under stress through population growth, urbanisation, water shortages, land and soil degradation, environmental pollution, world hunger and climate change.Hydroponics is a method to grow crops without soil, and as such, these systems are added to aquaculture components to create aquaponics systems. Thus, together with the recirculating aquaculture system (RAS), hydroponic production forms a key part of the aqua-agricultural system of aquaponics. Many different existing hydroponic technologies can be applied when designing aquaponics systems. This depends on the environmental and financial circumstances, the type of crop that is cultivated and the available space. This chapter provides an overview of different hydroponic types, including substrates, nutrients and nutrient solutions, and disinfection methods of the recirculating nutrient solutions

Timing of 15N fertiliser application, partitioning to reproductive and vegetative tissue, and nutrient removal by field-grown low-chill peaches in the subtropics

The effect of timing of nitrogen (N) application as N-enriched ammonium sulfate (50 kg N/ha) on the growth response and N uptake by vegetative and reproductive tissues was investigated in the low-chill peach cv. Flordagem growing on a krasnozem soil at Alstonville. Nitrogen was applied in late August, late September, late October, mid February, and early May. Tree parts were sampled for N at 4 and 8 weeks after application and after fruit harvest in December the following season. After fruit yield was measured, trees were excavated and divided into parts for dry weight and nutrient concentration determinations, and fertiliser N recovery and to estimate tree nutrient removal. Nitrogen enrichment was detected in all plant parts within 4 weeks of N application, irrespective of timing, and was greatest in rapidly growing tissues such as laterals, leaves, and fruit. The most rapid (P < 0.05) N enrichment in vegetative tissues resulted from September, October, and February N applications and for fruit from a September application. The level of enrichment 4 weeks after fertiliser N application was similar for vegetative and reproductive tissues. The timing of N application in the first season had no effect on fruit yield and vegetative growth the following season. At tree removal, the recovery of fertiliser N in most tree parts increased (P < 0.05) as fertiliser N application was delayed from October to May the previous season. Maximum contribution of absorbed N to whole tree N was 10-11% for laterals, leaf, and fruit. Data from this study indicate that vegetative and reproductive growth have similar demand for absorbed N, and that uptake of fertiliser N is most rapid when an application precedes a period of rapid growth. Over 2 seasons, recovery of applied fertiliser N was 14.9-18.0% in the tree, confirming that stored N and the soil N pool are the dominant sources of tree N. The recovery of fertiliser N from the May application was 18% even though uptake in all tree parts including roots at 4 weeks after application was very low, indicating that tree fertiliser N uptake occurred when growth resumed after the dormant winter period. The low proportion and recovery of fertiliser N in the tree confirm the lack of immediate influence of applied N to vegetative growth and yield. Annual crop nutrient removal is a sound basis for fertiliser recommendations, and for the Flordagem orchard (1000 trees/ha), it consisted of fruit plus 70% of laterals (removed at pruning) plus 20% of leaf. Removal in vegetative tissues was relatively low at (kg/ha) 14 N, 1 P, 12 K, 13 Ca, and 2 Mg. The addition of fruit at a yield of 25 t/ha increased total nutrient removal to (kg/ha) 46 N, 5 P, 54 K, 14 Ca, and 5 Mg