Knowledge of how plants will partition their new biomass will aid in understanding competition between crops and weeds. This study determined if the amount of biomass partitioned to the root versus the shoot can be predicted from tissue carbon [C] and nitrogen [N] concentrations and the daily gain in C (GC) and N (GN) for each unit shoot and root biomass, respectively. Pots measuring 28 cm diameter and 60 cm deep were embedded in the ground, and each contained one plant of either corn or velvetleaf. Each plant received one of three nitrogen treatments: 0, 1, or 3 g of nitrogen applied as ammonium nitrate in 2001 and 0, 2, or 6 g of nitrogen in 2002. Measurements of total above- and belowground biomass and tissue [C] and [N] were made at 10 different sample dates during the growing season. Fraction of biomass partitioned to roots (Pr) was predicted from [C], [N], GC, and GN. Accurate prediction of the fraction of biomass partitioned to roots versus shoots was evaluated by comparing observed and predicted Pr across all treatments. The coordination model has potential as a reliable tool for predicting plant biomass partitioning. Normalized error values were close to zero for corn in 2001 and 2002 and for velvetleaf in 2001, indicating that biomass partitioning was correctly predicted.

Competitive outcome between crops and weeds is affected by partitioning of new biomass to above- and belowground plant organs in response to nutrient supply. This study determined the fraction of biomass partitioned to roots vs. shoots in corn and velvetleaf in response to nitrogen (N) supply. Pots measuring 28 cm in diam and 60 cm deep were embedded in the ground and each contained one plant of either corn or velvetleaf. Each plant received one of three N treatments: 0, 1, or 3 g N applied as ammonium nitrate in 2001, and 0, 2, or 6 g N in 2002. Measurements of total above- and belowground biomass were made at 10 sampling dates during each growing season. The root:shoot ratio decreased over time for both corn and velvetleaf as a result of normal plant growth and as N supply increased. Root:shoot ratio was greater for corn than for velvetleaf at comparable stages of development and at all levels of N supply. Both corn and velvetleaf display true plasticity in biomass partitioning patterns in response to N supply. Velvetleaf root:shoot ratio increased by 46 to 82% when N was limiting in 2001 and 2002, respectively, whereas corn root:shoot ratio increased by only 29 to 45%. The greater increase in biomass partitioned to roots by velvetleaf might negatively impact its ability to compete with corn for light when N supply is limited.

Growth responses of two provenances of European beech (Fagus sylvatica) were studied. The seedlings were grown in closed-top chambers at four temperature regimes (−2.9 °C below ambient, ambient, +2.3 °C and +4.8 °C above ambient) in combination with two CO2 partial pressures (40 Pa and 74 Pa). Growth was followed by making destructive harvests c. every 25 d from germination in early June to senescence in late September. Allocation patterns were significantly affected by the temperature regimes. However, changes in dry matter allocation and morphology associated with the different treatments at a given time were mostly a result of differences in tree size. Temperature regimes only had a significant effect on the relative growth rate, RGR, at the beginning of the experiment. In contrast to temperature, high [CO2] increased RGR throughout the experiment when compared with plants of equal size. As the trees increased in size net assimilation rate, NAR, decreased but the effect of [CO2] on both NAR and RGR had a tendency to increase. Increases in NAR caused by elevated [CO2] were partly counteracted by reductions in the leaf area ratio, LAR. Reductions in LAR were caused by concomitant reductions in specific leaf area, SLA, whereas the level of [CO2] did not significantly affect leaf weight ratio, LWR, nor other dry weight ratios. The interactions between temperature and [CO2] are highly dependent on whether they are expressed as instantaneous values for plants at a common age or instantaneous values at a common size (and thereby extracting the effects of ontogenetic drift). When comparing instantaneous values at common sizes, the positive effect of [CO2] on RGR increased with plant size in every temperature regime. This also occurred in every temperature regime when comparing plants of equal age but the response to [CO2] was less. The effect of [CO2] on RGR was dependent on growth temperature. The positive effects of elevated [CO2] on RGR were less than the positive effect on photosynthesis. The two provenances did not differ significantly in the response of RGR to [CO2] which is in agreement with measurements of photosynthesis.