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Alternatively, other factors associated with leaf morphogenesis may be pleiotropic with leaf width, such as stomatal density or leaf thickness, and these may form the basis for the connection between leaf width and ∆13C.
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Interestingly, a positive correlation was found between flag leaf width and yield per plant.
Leaf length (L. L). and thickness (L. D). were significantly affected by induction of tetraploidy (P < 0.01), however no significant difference was observed between leaf width (L. W). of different ploidy levels (Figure 2; Table 3).
Significant differences were observed in morphological traits such as tree height, tree diameter, leaf width and leaf area between plants from RS and SM locations, resulting in smaller plants and smaller leaf size in SM plants.
There were no significant differences in leaf width and guard cell length between the OE-1 line and WT plants.
It indicated that the allele from PA64s affect flag leaf width and yield per plant at qFLW7.2 between INDEL7-2 and INDEL7-3, approximately 27.1 kb physical distance (Figure 6A).
The micropropagated plants showed significantly higher values for leaf area, leaf length, leaf width and leaf dry mass.
∆13C was negatively correlated with leaf width and leaf length (r = −0.3 in E2, r = −0.4 in E4), while leaf length was positively correlated with leaf width in both populations (r = 0.4 in E2, in E3, and in E4).
Fig. 6 Fourth leaf width and guard cell size in WT and transgenic lines.
Romaine lettuce growth periods, height, leaf width, and number of leaves were measured every week.
Furthermore, qGN4.1 caused a significant increase in flag leaf width and panicle branching in most backgrounds.
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