Content of nutritional elements in sudangrass and ryegrass determined by ICP-AES.

The sudangrass (Sorghum sudanense) and ryegrass (Lolium multi florum L.) rotation is a new type of cropping system, which has developed rapidly in recent years in the south of China. The contents of nutritional elements for forage grass in the sudangrass and ryegrass rotation system were determined by ICP-AES. The results showed that there were abundant and essential nutritional elements for animals in sudangrass and ryegrass. The contents of P, K, Ca, Mg, S, Fe, B, Cu, Zn and Mn for sudangrass were 0.20% -0.29%, 1.94%-2.57%, 0.62%-0.97%, 0.39%-0.69%, 0.12%-0.18%, 108.35-180.12, 3.04-5.96, 6.17-10.02, 20.37-31.36 and 46.80-101.29 mg x kg(-1), respectively. The contents of P, K, Ca, Mg, S, Fe, B, Cu, Zn, Mn for ryegrass were 0.39%-0.70%, 3.77%-5.07%, 0.61%-0.84%, 0.28% -0.47%, 0.32%-0.41%, 291.65- 632.20, 2.13-3.23, 13.29-15.19, 30.73-42.98 and 92.08-156.04 mg x kg(-1), respectively, and there were differences between various periods in nutritional elements in the two forage grasses. The application of ICP-AES could reflect fast and efficiently the content of nutritional elements for forage grass as animals feed.

Canopy development and hydraulic function in Eucalyptus tereticornis grown in drought in CO2-enriched atmospheres.

We report on the relationship between growth, partitioning of shoot biomass and hydraulic development of Eucalyptus tereticornis Sm. grown in glasshouses for six months. Close coordination of stem vascular capacity and shoot architecture is vital for survival of eucalypts, especially as developing trees are increasingly subjected to spasmodic droughts and rising atmospheric CO2 levels. Trees were exposed to constant soil moisture deficits in 45 L pots (30-50% below field capacity), while atmospheric CO2 was raised to 700 µL CO2 L-1 in matched glasshouses using a hierarchical, multi-factorial design. Enrichment with CO2 stimulated shoot growth rates for 12-15 weeks in well-watered trees but after six months of CO2 enrichment, shoot biomasses were not significantly heavier (30% stimulation) in ambient conditions. By contrast, constant drought arrested shoot growth after 20 weeks under ambient conditions, whereas elevated CO2 sustained growth in drought and ultimately doubled the shoot biomass relative to ambient conditions. These growth responses were achieved through an enhancement of lateral branching up to 8-fold due to CO2 enrichment. In spite of larger transpiring canopies, CO2 enrichment also improved the daytime water status of leaves of droughted trees. Stem xylem development was highly regulated, with vessels per unit area and cross sectional area of xylem vessels in stems correlated inversely across all treatments. Furthermore, vessel numbers related to the numbers of leaves on lateral branches, broadly supporting predictions arising from Pipe Model Theory that the area of conducting tissue should correlate with leaf area. Diminished water use of trees in drought coincided with a population of narrower xylem vessels, constraining hydraulic capacity of stems. Commensurate with the positive effects of elevated CO2 on growth, development and leaf water relations of droughted trees, the capacity for long-distance water transport also increased.

Changes in sourcesink relations during development influence photosynthetic acclimation of rice to free air CO2 enrichment (FACE).

Relationships between photosynthetic acclimation and changes in the balance between source-sink supply and demand of carbon (C) and nitrogen (N) were tested using rice (Oryza sativa L. cv. Akitakomachi). Plants were field-grown in northern Japan at ambient CO2 partial pressure [p(CO2)] or free air CO2 enrichment (FACE; p(CO2) ~ 26-32 Pa above ambient) with low, medium or high N supplies. Leaf CO2 assimilation rates (A) and biochemical parameters were measured at 32-36 (eighth leaf) and 76-80 (flag leaf) d after transplanting, representing stages with a contrasting balance between C and N supply and demand in sources and sinks. Acclimation due to FACE was pronounced in flag leaves at each N supply. This was not fully accounted for by reductions in leaf N concentrations, because A/N and Vcmax/N were lower in FACE-grown flag leaves. Acclimation did not occur in the eighth leaf, and A/N and Vcmax/N was not significantly increased in FACE-grown leaves. Soluble protein / sucrose and amino acid / sucrose concentrations decreased under FACE, whereas sucrose phosphate synthase protein levels increased. At flag leaf stage, there was a discrepancy between the demand and supply of N, which was resolved by enhanced leaf N remobilization, associated with the lower Rubisco concentrations under FACE. In contrast to the early growth stage, enhanced growth of rice plants was accompanied by increased plant N uptake in FACE. We conclude that photosynthetic acclimation in flag leaves occurs under FACE because there is a large demand for N for reproductive development, relative to supply of N from root uptake and remobilization from leaves.