“…This possibility is of great interest in environmental biogeochemistry because (i) the differences between spectra are often subtle and (ii) the improved resolution gives a more precise discrimination of the local structure around the absorbing atom. This possibility was, for example, fully exploited at the Fe K‐edge probing the Fe K β1,3 fluorescence line to study biomineralization processes (Baumgartner et al, 2013), to study magnetite nanoparticle evolution during conversion of biomass (Casals et al, 2014), at the Ce L III edge to characterize the behavior of cerium oxide nanoparticles in aquatic mesocosms (see below; Tella et al, 2015), or at the Hg L III edge to determine which chemical forms of Hg are present in human hair (Manceau et al, 2016). To highlight in more detail this real step forward, XANES measurements in conventional methods (transmission or total fluorescence yield measurement) and in HERFD are presented below to ascertain the valence state of Ce, in the case of biotransformation of CeO 2 nanoparticles, and the speciation of Hg bound to sulfur.…”