Experimental Evidence of Harnessed Expansion of a High-Z Plasma Using the Hollow Wall Design for Indirect Drive Inertial Confinement Fusion.

The effectiveness of a dome-shaped wall covered by a thin gold foil (hollow wall) [M. Vandenboomgaerde et al., Phys. Plasmas 25, 012713 (2018)PHPAEN1070-664X10.1063/1.5008669] in holding back the high-Z plasma expansion in a gas-filled hohlraum is demonstrated for the first time in experiments reproducing the irradiation conditions of indirect drive at the ignition scale. The setup exploits a 1D geometry enabling record of the complete history of the gold expansion for 8 ns by imaging its emission in multiple x-ray energy ranges featuring either the absorption zones or the thermal emission regions. The measured expansion dynamics is well reproduced by numerical simulations. This novel wall design could now be tailored for the megajoule scale to enable the propagation of the inner beams up to the equator in low gas-filled hohlraum thus allowing the fine-tuning of the irradiation symmetry on the timescale required for ignition.

Qualitative and quantitative molecular detection of enteroviruses in water from bathing areas and from a sewage treatment plant.

Pathogenic enteric viruses can be introduced into the environment as a result of human activities. Enteroviruses are regularly detected in environmental waters or shellfish and can provoke potentially serious diseases. Some authors believe that enteroviruses could represent an interesting indicator of viral contamination in the environment. Since molecular approaches seem to be promising for the detection of these viruses, we developed a simple qualitative RT-PCR procedure for enteroviruses, together with a quantitative RT-PCR assay using RNA internal standard. After one-tube-RT-PCR, this standard and wild enterovirus RNA were detected by differential hybridization with specific probes and a fluorimetric reaction. The quantification of enteroviruses, conducted in a sewage treatment plant, showed a decreasing number of genomic copies from the entrance to the exit (from 3.8 x 10(5) to 5.4 x 10(4) RNA copies/mL) but indicated the presence of enterovirus RNA in the neighboring river (2.2 x 10(3) RNA copies/mL). In bathing areas, enterovirus RNA was detected in 16 out of 226 samples, with copies numbers ranging from 3.7 x 10(2) RNA copies/mL to 7 x 10(4) RNA copies/mL.