E. Justes et al., Effect of crop nitrogen status and temperature on the radiation use efficiency of winter oilseed rape, EUR J AGRON, 13(2-3), 2000, pp. 165-177
In temperate environments, the total dry matter (TDM) of a crop is closely
related to the amount of photosynthetically active radiation absorbed (Sigm
a PARa), as long as other factors (water, nutrients,...) are non-limiting.
For oilseed rape crops, many authors have shown that the radiation use effi
ciency (RUEa) varies within a wide range, from 1 to 4 g MJ(-1) of Sigma PAR
a according to developmental stage and environmental conditions. In order t
o explain this variability, effects of N and temperature on RUEa were inves
tigated during a 1-year field experiment involving three N treatments (N fe
rtilisation rates: 0, 135 and 270 kg ha(-1)). Leaf, flower, and pod surface
areas, as well as the DM and N content of the various plant parts were mea
sured every 2-4 weeks for 17 sampling dates from emergence to harvest. RUEa
was calculated from total generated DM (shoot and root DM, plus that of de
ad leaves fallen to the ground). Daily PARa was calculated using a 3-layer
model laking into account leaf and pod absorption and reflection of PAR by
flowers and soil. The N nutrition index (NNI) proposed by Lemaire and Gasta
l (1997) was used to evaluate the N effect on RUEa. NNI was significantly h
igher than the critical N value (meaning that N was non-limiting) for the N
270 treatment from emergence to pod formation, but N deficiency occurred wi
th NO at the 12-leaf stage and later with N135 at flowering. The maximum po
ssible RUEa (RUEa(max)) was assumed to be the value obtained with the treat
ment N270, where N was non-limiting. The N deficiencies which occurred for
NO and N135 significantly reduced the green LAI and PAI, and consequently S
igma PARa. To remove any effect other than N on the RUEa, the ratio of actu
al to maximum RUEa (RUEa/RUEa(max)) proposed by Belanger et al. (1992) was
calculated for each developmental stage of oilseed rape. A linear regressio
n fit well (R-2=0.919; 8 d.f.) the response of RUEa/RUEa(max) versus N defi
ciency, for values of NNI lower than 1. The resulting equation was the foll
owing: RUEa/RUEa(max) = 0.74 x NNI + 0.23. RUEa(max) was also significantly
affected by developmental stage. Whereas the corresponding changes in RUEa
(max) from the 6-leaf stage to the end of flowering could be related to air
temperature, there was evidence of a developmental effect in the other sta
ges. RUEa was lower in the early stages (emergence to 5-6 leaves), and from
pod formation until ripening; the latter decrease could be attributed to t
he high energy cost of lipid biosynthesis. (C) 2000 Elsevier Science B.V. A
ll rights reserved.