Table III.
Day | Photoperiod | 15NH4+ Assimilation | Carbohydrate
|
|||
---|---|---|---|---|---|---|
Requirementa | Change in shoot | Change in root | Transport to rootb | |||
μmol N plant−1 | μmol C plant−1 | |||||
7–8 | Dark | 39 ± 4 | 117 ± 13 | −319 ± 7 | −57 ± 10 | 60 ± 15 |
8 | Light | 102 ± 18 | 310 ± 53 | +556 ± 35 | +61 ± 7 | 371 ± 55 |
8–9 | Dark | 91 ± 11 | 275 ± 34 | −550 ± 12 | −103 ± 6 | 172 ± 37 |
9 | Light | 110 ± 24 | 333 ± 74 | +590 ± 67 | +42 ± 11 | 375 ± 64 |
9–10 | Dark | 120 ± 28 | 365 ± 84 | −501 ± 24 | −38 ± 13 | 327 ± 97 |
10 | Light | 288 ± 30 | 872 ± 91 | +1193 ± 147 | +118 ± 21 | 990 ± 108 |
The diurnal assimilation of 15NH4+ was measured during a 3-d exposure of maize seedlings to highly labeled 15NH4+. The minimal transport of C from shoot to root required to support 15NH4+ assimilation was calculated from the theoretical C requirement for 15NH4+ assimilation and the changes in tissue carbohydrate. Each value is the mean of four replicates ± se.
Calculation of the total C requirement for 15NH4+ assimilation is based on the assumption that assimilation of entering 15NH4+ occurs in the root, and that the initial product of NH4+ assimilation is Gln, which requires 0.505 mol of Glc equivalents mol−1 NH4+ to provide the necessary reductant, ATP, and C skeletons (Schubert, 1982).
Minimal C transport to the root required to support 15NH4+ assimilation is equal to the total C required for 15NH4+ assimilation plus the change in root C content.