“…Dense media separation may either be undertaken at a single target density (e.g., 1.5 times the density of water, or 1.5 SG) in which pollen grains, which have a typical density of slightly less than 1.5 SG (Régnell and Everitt 1992), float, or at a series of decreasing densities (e.g., from 1.6-1.15 SG), allowing selection of the purest residue(s) for dating (Vandergoes and Prior 2003). Alternatives to density separations include manual selection of individual grains using a micromanipulator (e.g., Long, Davis, and De Lanois 1992), and isolation of pollen grains using flow cytometry (Tennant et al 2013). However, the former technique is generally too time-consuming to be practical unless very large pollen grains such as Picea are abundant, and the latter has yet to be routinely applied for radiocarbon dating.…”