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. 2016 Nov 8;5(12):1806–1820. doi: 10.1242/bio.021402

Fig. 1.

Fig. 1.

D14 mediates SL signalling in the adult shoot. (A) Rosette leaf phenotypes in candidate SL signalling mutants 4 weeks after germination. (B) Branching phenotypes in candidate SL signalling mutants 6 weeks after germination. (C) Dark-induced leaf senescence phenotypes in candidate SL signalling mutants. Rosette leaves were wrapped in foil for 8 days then imaged. (D) Leaf dimensions in candidate SL signalling mutants. Measurements were made on the seventh rosette leaf, 35 days after germination. n=10-12, bars indicate s.e.m. Bars with the same letter are not significantly different from each other (ANOVA, Tukey HSD test). (E) Branching levels in candidate SL signalling mutants. Numbers of primary cauline and rosette branches were measured at proliferative arrest, n=10-12, bars indicate s.e.m. Bars with the same letter are not significantly different from each other (ANOVA, Tukey HSD test). (F) Branch angle (measured in degrees) in candidate SL signalling mutants, n=10-12, bars indicate s.e.m. Bars with the same letter are not significantly different from each other (ANOVA, Tukey HSD test).