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. 2023 Jul 19;13:11645. doi: 10.1038/s41598-023-38790-7

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© The Author(s) 2023

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 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/.

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Effect of maternal genotype on intraspecific chemodiversity. (a) Variation partitioning on 52 GC–MS features (ANOVA test, P < 0.05). (b) Variation partitioning on 5,066 LC–MS features (ANOVA test, P < 0.05). (c) R² scores of the 500 generalised linear models using GC–MS or LC–MS features (Tukey’s test, P < 0.01). For each condition, 500 permuted datasets were developed. Feat: features, Perm: permuted. Sig: significant. “GC–MS Sig feat” included 41 significant features, “LC–MS Sig feat” contained 3,688 significant features and “LC–MS Top 5%” included the best 5% markers (184). (d) Putative annotation of the best LC–MS markers.