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. 2022 Mar 8;16(6):1657–1667. doi: 10.1038/s41396-022-01214-x

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© The Author(s) 2022

Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.

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Fig. 5 — Maps of the relative abundance (a) of total jumbo phages (in RPKM) and (b) total number of jumbo populations present regardless of phage cluster membership in each surface (SRF) sample of the picoplankton size fraction (either 0.22–3 μm or 0.22–1.6 μm depending on availability). Dots sizes are proportional to the number of populations or RPKM. c Scatterplot of the mean RPKM of a jumbo population in SRF picoplankton samples versus the number of SRF picoplankton stations it was present. Populations are colored by PGC and size corresponds to putative genome length in 100 kilobases. d Boxplot of the number of jumbo phage populations in samples co-collected at each depth sorted by mean for each PGC. Significance bars correspond to Wilcox tests, with stars corresponding to p values < 0.05 (* < 0.05, ** < 0.01, *** < 0.001, **** < 0.0001) (stat_compare_means function).