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. 2021 Jan 22;9:24. doi: 10.1186/s40168-020-00974-y

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© The Author(s) 2021

Open AccessThis 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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.

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Fig. 6 — Distribution of pairwise Bray–Curtis dissimilarity for amplicon sequence variant (ASV) compositions among the nine Japanese lakes. Each point represents the dissimilarity between a pair of the samples, and their distribution is represented by a boxplot for each lineage. Note that dissimilarity is 1 when there are no shared ASVs between two samples, and thus many points are concentrated on the top of the boxes. The original pairwise dissimilarity matrices are available in Fig. S3. Note that acI-C2 comprised two different operational taxonomic units that were specific to the epilimnion (acI-C2-e) and hypolimnion (acI-C2-h), respectively