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. 2019 Sep 30;71(7):2299–2311. doi: 10.1093/jxb/erz439

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© The Author(s) 2019. Published by Oxford University Press on behalf of the Society for Experimental Biology.

This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com

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Fig. 1. — Wheat and triticale germplasm was measured for (A) A, (B) g_s, (C) C_i/C_a, (D) V_cmax25, (E) J, (F) J/V_cmax25, (G) LMA, (H) N_area, and (I) SPAD, in three experiments measured in Australia (Aus1, Aus2, and Aus3) and one in Mexico (Mex1). Some experiments were set up in the glasshouse (GH) and others in the field. Three sets of genotypes were assessed: Early Vigour set, EV (pink); BUNYIP set, BYP (purple); and CIMCOG set, C (blue). An extra ‘B’ in the acronyms means measured before anthesis and an extra ‘A’ means after anthesis. The numbers of genotypes measured are in parentheses. The coloured section is the interquartile range (IQR), representing 50% of the data. The lower IQR edge is the point at 25% of the data. The middle black point is the mean, and the line is the median. The upper IQR edge is the 75% point. The whiskers are 1.5 times the IQR, showing the minimum and maximum data. Circles are outliers.