taxonID	type	description	language	source
84578797FFA6622EE917FDFD7F97D96F.taxon	description	The amplifications were conducted in a 96 + Grad 1000 S thermocycle, programmed as follows: initial denaturation step at 98 ° C for 30 sec, followed by 35 cycles of denaturation steps at 98 ° C for 5 sec, an annealing step at 55 ° C for 5 sec, extension step at 72 ° C for 15 sec; final extension at 72 ° C for 1 min. PCR results were checked in standard 1 % agarose gel electrophoresis. Gels were stained and immersed in 0.5 μg / ml ethidium bromide solution for 30 min, visualized and recorded on a Gel Doc Systems (Bio-Rad, Barcelona, Spain; https: // www. bio-rad. com /). All selected PCR amplification products were sent to BaseClear (https: // www. baseclear. com). The resulting chromatograms were then assembled and edited using Sequencher ™ 4.1.4 (Gene Codes Corp., Ann Arbor, Michigan, USA; https: // genecodes. com /). To ensure that the DNA isolated was not contaminated, all sequences were BLAST-searched in GenBank. The sequence results of all markers were submitted to the NCBI GenBank sequence database (see Appendix 1).	en	Atria, M., Eurlings, M., Baker, W. J., Dransfield, J., Welzen, P. C. van (2020): Phylogenetic analysis of the Calamus javensis complex (Arecaceae: Calamoideae) in Malesia. Blumea 65 (3): 205-211, DOI: 10.3767/blumea.2020.65.03.04, URL: https://doi.org/10.3767/blumea.2020.65.03.04
