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- Murari, A., et al.
(författare)
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A control oriented strategy of disruption prediction to avoid the configuration collapse of tokamak reactors
- 2024
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Ingår i: Nature Communications. - 2041-1723 .- 2041-1723. ; 15:1
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Tidskriftsartikel (refereegranskat)abstract
- The objective of thermonuclear fusion consists of producing electricity from the coalescence of light nuclei in high temperature plasmas. The most promising route to fusion envisages the confinement of such plasmas with magnetic fields, whose most studied configuration is the tokamak. Disruptions are catastrophic collapses affecting all tokamak devices and one of the main potential showstoppers on the route to a commercial reactor. In this work we report how, deploying innovative analysis methods on thousands of JET experiments covering the isotopic compositions from hydrogen to full tritium and including the major D-T campaign, the nature of the various forms of collapse is investigated in all phases of the discharges. An original approach to proximity detection has been developed, which allows determining both the probability of and the time interval remaining before an incoming disruption, with adaptive, from scratch, real time compatible techniques. The results indicate that physics based prediction and control tools can be developed, to deploy realistic strategies of disruption avoidance and prevention, meeting the requirements of the next generation of devices.
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- Mpetha, C. T., et al.
(författare)
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Gravitational redshifting of galaxies in the SPIDERS cluster catalogue
- 2021
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Ingår i: Monthly notices of the Royal Astronomical Society. - : Oxford University Press (OUP). - 0035-8711 .- 1365-2966. ; 503:1, s. 669-678
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Tidskriftsartikel (refereegranskat)abstract
- Data from the SPectroscopic IDentification of ERosita Sources (SPIDERS) are searched for a detection of the gravitational redshifting of light from ∼20000 galaxies in ∼2500 galaxy clusters using three definitions of the cluster centre: its Brightest Cluster Galaxy (BCG), the redMaPPer identified Central Galaxy (CG), or the peak of X-ray emission. Distributions of velocity offsets between galaxies and their host cluster’s centre, found using observed redshifts, are created. The quantity ˆΔ, the average of the radial velocity difference between the cluster members and the cluster systemic velocity, reveals information on the size of a combination of effects on the observed redshift, dominated by gravitational redshifting. The change of ˆΔ with radial distance is predicted for SPIDERS galaxies in General Relativity (GR), and f(R) gravity, and compared to the observations. The values of ˆΔ=−13.5±4.7 km s−1, ˆΔ=−12.5±5.1 km s−1, and ˆΔ=−18.6±4.8 km s−1 for the BCG, X-ray, and CG cases, respectively, broadly agree with the literature. There is no significant preference of one gravity theory over another, but all cases give a clear detection (>2.5σ) of ˆΔ. The BCG centroid is deemed to be the most robust method in this analysis, due to no well-defined central redshift when using an X-ray centroid, and CGs identified by redMaPPer with no associated spectroscopic redshift. For future gravitational redshift studies, an order-of-magnitude more galaxies, ∼500000, will be required – a possible feat with the forthcoming Vera C. Rubin Observatory, Euclid and eROSITA.
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- Cespedes, PF, et al.
(författare)
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T-cell trans-synaptic vesicles are distinct and carry greater effector content than constitutive extracellular vesicles
- 2022
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Ingår i: Nature communications. - : Springer Science and Business Media LLC. - 2041-1723. ; 13:1, s. 3460-
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Tidskriftsartikel (refereegranskat)abstract
- The immunological synapse is a molecular hub that facilitates the delivery of three activation signals, namely antigen, costimulation/corepression and cytokines, from antigen-presenting cells (APC) to T cells. T cells release a fourth class of signaling entities, trans-synaptic vesicles (tSV), to mediate bidirectional communication. Here we present bead-supported lipid bilayers (BSLB) as versatile synthetic APCs to capture, characterize and advance the understanding of tSV biogenesis. Specifically, the integration of juxtacrine signals, such as CD40 and antigen, results in the adaptive tailoring and release of tSV, which differ in size, yields and immune receptor cargo compared with steadily released extracellular vesicles (EVs). Focusing on CD40L+tSV as model effectors, we show that PD-L1 trans-presentation together with TSG101, ADAM10 and CD81 are key in determining CD40L vesicular release. Lastly, we find greater RNA-binding protein and microRNA content in tSV compared with EVs, supporting the specialized role of tSV as intercellular messengers.
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