Abstract
Summary
Comparing maize canopies is confounded by two problems: plants differ in the number of phytomers they produce, and phytomer size scales with that number. Position along the shoot is therefore an unreliable basis for comparison, confounding shape with size.
We first position the floral transition (tassel initiation, T.I.) within shoot development, revealing it as the landmark that organizes a conserved canopy shape. This provides the foundation for aligning canopies that differ in phytomer number.
Focusing on the leaf blade, we used functional data analysis on a maize panel across controlled and field environments to decompose variation in blade-length profiles, which was dominated (77%) by overall amplitude, identifying scaling as the major source of size variation. Because blades enlarge with each phytomer until the transition, later T.I. yields a larger maximum; this T.I.-linked component explains up to one-third of scaling variation, reinforced by a shared genetic association between T.I. and blade size with the flowering-time gene
ZmCCT10
.
Regressing out this component leaves a residual that defines a new, heritable axis of intrinsic scaling, independent of flowering time. It distinguishes hyper- and hypo-scaling genotypes consistently across environments, offering a selection target decoupled from phenology.
Plain Language Summary
Plants vary in how many leaves they grow and how big those leaves get, making canopies hard to compare across different varieties and growing conditions. Studying maize, we found that the timing of flowering organizes the overall shape of the canopy, letting us compare them fairly, and uncovered a separate, inherited source of leaf-size variation. This could help breeders adjust crop canopies without changing when plants flower.