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. 2020 Mar 30;13:188. doi: 10.1186/s13104-020-05035-z

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© The Author(s) 2020

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. 2 — Larval resistance to nicotine is impacted by deletions in Ugt86Dd. Each strain was tested in both control (C) and nicotine (N) treatments. The fraction of adults emerging from each replicate vial is shown by asterisk and cross symbols, while the genotype/treatment means (± 1-SD) are shown by colored whiskers. Nicotine viability is lower than control viability for all strains with a deletion in Ugt86Dd (red and blue whiskers; see Table 1)