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. 2014 Dec 11;66(5):1317–1324. doi: 10.1093/jxb/eru482

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© The Author 2014. 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 License (http://creativecommons.org/licenses/by/3.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.

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Fig. 3. — Plastochrone in clasp-1, Col-0, and WS-4. (A) Cumulated number of newly opened flowers in clasp-1 (n=16), Col-0 (n=24), and WS-4 (n=17). (B) Mean plastochrone calculated from the first 10 d of flower production (two-tailed Student test). (C) Representative clasp-1, Col-0, and WS-4 meristems expressing the pAHP6::GFP marker of organ identity, using the ImageJ Fire lookup table. Scale bars=20 μm. (D) Mean size difference between successive primordia in clasp-1, 147 organs, 26 meristems; Col-0, 148 organs, 23 meristems; WS-4, 161 organs, 20 meristems, two-tailed Student tests. (E) Quantification of the number of GFP-positive stage 1 and stage 2 primordia in clasp-1 (n=12 meristems), Col-0 (n=20 meristems), and WS-4 (n=17 meristems), two-tailed Student tests.