The estimation of demographic parameters in natural populations is a critical tool for species delimitation (Duminil and Di Michele, 2009), biogeography studies (Overcast et al., 2019), and monitoring of populations and species in a dynamically changing environment (Allendorf et al., 2010). The feasibility of estimating demographic parameters (including heterozygosity, effective population size, and levels of introgression) in non-model taxa relies on retrieving homologous markers that allow detection of sufficient variation across the genome, while remaining cost-effective for the analysis of hundreds of individuals. In plants, population genomic studies could benefit from markers that enable the further unlocking of herbarium specimens for botanical research, paralleling the impact of herbarium specimens in phylogenomics (e.g., Shee et al., 2020), microbiome research (e.g., Heberling and Burke, 2019), and studies of the effects of climate change on plant populations (e.g., Miller-Rushing et al., 2009). Traditional Sanger sequencing of PCR amplicons often employs universal primer sequences, but the genes targeted (e.g., the plastid markers matK and rbcL, or the nuclear ribosomal ITS) do not