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. 2009 May;150(1):494–505. doi: 10.1104/pp.109.138107

Table I.

ROS production in embryonic axes during imbibition

H2O2 and superoxide (O2·−) production in embryonic axes isolated from dormant (d) and after-ripened, nondormant (nd) sunflower embryos before imbibition (dry) and from embryos that were imbibed on water for 24 h at 10°C (H2O), or treated for 3 h with 0.1 mm MV (MV) or with gaseous cyanide (HCN) and then transferred for 21 h on water at 10°C. Values are means of five replicates ± sd. DW, Dry weight.

Treatment Duration of Imbibition H2O2
O2.−
d nd d nd
h nmol g DW−1 nmol g DW−1
No 0 (dry) 1.51 ± 0.21 2.10 ± 0.04 0.62 ± 0.03 0.91 ± 0.06
H2O 3 2.12 ± 0.13 2.96 ± 0.09 0.63 ± 0.01 0.98 ± 0.05
HCN 3 2.81 ± 0.12 4.22 ± 0.2 0.70 ± 0.06 1.01 ± 0.06
MV 3 2.73 ± 0.11 3.11 ± 0.15 0.70 ± 0.04 0.99 ± 0.06
H2O 24 2.50 ± 0.19 3.26 ± 0.17 0.61 ± 0.05 1.10 ± 0.06
HCN 24 4.25 ± 0.35 5.05 ± 0.11 0.67 ± 0.05 1.28 ± 0.06
MV 24 4.51 ± 0.17 5.44 ± 0.22 0.69 ± 0.03 1.20 ± 0.02