“…Straightforward spectroscopy of foil-excited ion beams suffers from the excitation of too many lines that can make identification difficult in the absence of high quality calculations. However, this drawback and the often considerable line width (unless refocusing techniques are employed [228][229][230][231][232]) are offset by the fact that the BFS light source is monoisotopic: with the exception of some few carbon UV lines (from the foil, possibly after sputtering), all the light is that of a defined element, and even the charge state can be determined within a few units by suitable beam energy variation. The accumulation of a 'complete' spectral data base of all elements and from the x-ray range to the visible or even to the near infrared would be of great scientific and applied science value, but, alas, it would also be prohibitively expensive in terms of accelerator time and manpower.…”