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. 2020 Sep 1;7:143. doi: 10.1038/s41438-020-00364-3

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© The Author(s) 2020

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. 1 — Apple cuttings were cultured in Hoagland’s solution and sampled every 24 hours (h) from 0 to 168 h. Three distinctive development phases were observed at 0, 72, and 168 h. a–g Physical appearance of submerged cuttings. Arrows point to the origination of new ARs. h–u SEM micrographs of lenticels at different AR developmental phases; Bars: a–g = 0.4 cm, h–u = 100 μm. Bars i = j = k; l = m = n; p = q = r; and s = t = u.