30 research outputs found
Searching for dark matter with plasma haloscopes
We summarize the recent progress of the Axion Longitudinal Plasma Haloscope (ALPHA) Consortium, a new experimental collaboration to build a plasma haloscope to search for axions and dark photons. The plasma haloscope is a novel method for the detection of the resonant conversion of light dark matter to photons. ALPHA will be sensitive to QCD axions over almost a decade of parameter space, potentially discovering dark matter and resolving the strong CP problem. Unlike traditional cavity haloscopes, which are generally limited in volume by the Compton wavelength of the dark matter, plasma haloscopes use a wire metamaterial to create a tuneable artificial plasma frequency, decoupling the wavelength of light from the Compton wavelength and allowing for much stronger signals. We develop the theoretical foundations of plasma haloscopes and discuss recent experimental progress. Finally, we outline a baseline design for ALPHA and show that a full-scale experiment could discover QCD axions over almost a decade of parameter space
Searching For Dark Matter with Plasma Haloscopes
We summarise the recent progress of the Axion Longitudinal Plasma HAloscope
(ALPHA) Consortium, a new experimental collaboration to build a plasma
haloscope to search for axions and dark photons. The plasma haloscope is a
novel method for the detection of the resonant conversion of light dark matter
to photons. ALPHA will be sensitive to QCD axions over almost a decade of
parameter space, potentially discovering dark matter and resolving the Strong
CP problem. Unlike traditional cavity haloscopes, which are generally limited
in volume by the Compton wavelength of the dark matter, plasma haloscopes use a
wire metamaterial to create a tuneable artificial plasma frequency, decoupling
the wavelength of light from the Compton wavelength and allowing for much
stronger signals. We develop the theoretical foundations of plasma haloscopes
and discuss recent experimental progress. Finally, we outline a baseline design
for ALPHA and show that a full-scale experiment could discover QCD axions over
almost a decade of parameter space.Comment: Endorsers: Jens Dilling, Michael Febbraro, Stefan Knirck, and Claire
Marvinney. 26 pages, 17 figures, version accepted in Physical Review
Child restraint systems : Measurement of opening force requirements of buckles exposed to loads of 60-200 N
The relationship between census results and the breeding population of birds in subalpine birch forests
How Local are Spatial Density Externalities? Neighbourhood Effects in Agglomeration Economies
Low dose erythropoietin is effective in reducing transfusion requirements following allogeneic HSCT
Long-term persistence of oligoclonal serum IgM repertoires in patients treated with allogeneic bone marrow transplantation (BMT)
Immunoglobulin gene rearrangements in patients treated with BMT have restricted repertoire diversity. Clonal variability remains low for 3 months and reconstitution of the humoral immune system appears to follow a wave-like pattern. In the present study we analysed serum IgM and IgG repertoires in 44 patients from 1 week to 3 years after transplantation. We applied a quantitative immunoblot technique in combination with a newly developed method for estimation of repertoire diversity in complex mixtures of antibodies. Our results demonstrate that 60% of BMT patients have severely reduced diversity in the IgM repertoire during and after the first year post-BMT, compared with healthy controls. In contrast, the majority of patients have a polyclonal IgG repertoire, similar to that of healthy controls. Serum IgM repertoires remain oligoclonal even though the serum concentration of total IgM is within normal range around 6 months post-BMT. During the first years after transplantation IgM as well as IgG repertoires are less diverse in patients receiving a BM graft from a sibling donor compared with those receiving a graft from an HLA-matched unrelated donor. Patients in the latter group show a higher incidence of infections and minor antigen mismatches which may promote the development of a diverse immunoglobulin repertoire post-BMT