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Abstract. There is little consensus on whether having a large root system is the best strategy in adapting wheat (Triticum aestivum L.) to water-limited environments. We explore the reasons for the lack of consensus and aim to answer the question of whether a large root system is useful in adapting wheat to dry environments. We used unpublished data from glasshouse and field experiments examining the relationship between root system size and their functional implication for water capture. Individual root traits for water uptake do not describe a root system as being large or small. However, the recent invigoration of the root system in wheat by indirect selection for increased leaf vigour has enlarged the root system through increases in root biomass and length and root length density. This large root system contributes to increasing the capture of water and nitrogen early in the season, and facilitates the capture of additional water for grain filling. The usefulness of a vigorous root system in increasing wheat yields under water-limited conditions maybe greater in environments where crops rely largely on seasonal rainfall, such as the Mediterranean-type environments. In environments where crops are reliant on stored soil water, a vigorous root system increases the risk of depleting soil water before completion of grain filling.Additional keywords: root biomass, root length, root length density, root system size, water capture.

Preanthesis stored C and N in wheat (Triticum aestivum L.) are important in a mediterranean climate because grain filling frequently depends on the remobilization of preanthesis assimilates. We determined the effect of the rate of development of postanthesis water deficits on the remobilization of C and N to the grain using stable isotopes of C and N accumulated in the plant during the vegetative phase. Plants were grown in pots with adequate water and under similar temperature and humidity conditions until anthesis, and then were transferred to two temperature and humidity regulated greenhouses, and watering was stopped. One greenhouse was maintained at minimum relative humidity of 80% and the other at 40%. Within 6 d of anthesis the rates of development of plant water deficits became different and for the first 19 d after anthesis they were 0.10 and 0.18 MPa d−1 for the high and low humidity regimes, respectively. Total grain C with fast development of water deficits was reduced by 24%, relative to the slow rate, because postanthesis C assimilation was reduced by 57%, while remobilization of preanthesis stored C was increased by 36%. Total grain N was not affected by the rate of development of water deficits because there was a greater retranslocation of preanthesis N with fast relative to slow development of water deficits and because there was a smaller loss of preanthesis N with fast development of water deficits. Fast development of water deficits reduced losses of preanthesis N from 25% to 6%. The absolute contributions of preanthesis C and N to the grain were 449 and 35 mg plant−1, respectively, with fast development of water deficits. These contributions accounted for 64 and 81% of the total grain C and N, respectively. The gain in grain 13C and 15N in the mainstem and Tiller 1 of plants exposed to rapid development of water deficits, arose not only from remobilization from the straw of those shoots, but also seemed to be supplemented by C and N remobilized from Tillers 2 and 3.

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Root growth is important for the acquisition of nitrogen (N) and water in deep sandy soil profiles with high leaching potential. Root growth characteristics and the N uptake of wheat genotypes differing in early vigour were investigated in 2 glasshouse experiments. In both experiments the vigorous breeding lines Vigor18 and B18 and the well-adapted commercial cultivar Janz were grown in glass-walled growth boxes in a controlled-temperature glasshouse up to the onset of stem elongation. In Expt 1, rooting parameters and detailed measurements of root growth and proliferation were made at 2-day intervals using a root mapping technique. In Expt 2 the glass-walled growth boxes were segmented into upper (0–0.2 m), middle (0.2–0.7 m), and bottom (0.7–1.0 m) soil layers, and the contribution of N fertiliser uptake by roots from each soil layer to the total plant N uptake was determined by applying 15N-urea to a single soil layer each time. The accumulated total root length across the soil profile from the 1-leaf stage to the onset of stem elongation was 33–83% higher in the vigorous lines Vigor18 and B18 than in Janz. The roots of the 3 genotypes grew vertically down the soil profile at a similar rate, but the roots of vigorous lines branched earlier and grew horizontally faster and more extensively than those of cv. Janz, resulting in a greater root-length density and root number in the top 0.7-m soil layer. Uptake of N fertiliser by roots in the upper 0–0.2 m of the soil profile was 60–68% higher in the vigorous lines than in Janz. Roots of the vigorous lines located in the segment 0.2–0.7 m of the soil profile captured twice as much N fertiliser than those of Janz. Uptake of N fertiliser by roots in the lower 0.7–1.0 m of the soil profile was similar in the vigorous lines and Janz. This indicates that the early and more extensive horizontal growth of the roots in the 0.2–0.7 m of the soil profile was responsible for the superior uptake of N by the vigorous lines. The implications of these genotypic differences in root growth and proliferation and their relationship with the early acquisition of N are discussed with emphasis on their role in improving the efficiency of N fertiliser uptake and reducing nitrate leaching, particularly in the sandy soils of the Mediterranean climatic region of Australia.

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The response of wheat crops to elevated CO 2 (eCO 2) was measured and modelled with the Australian Grains Free‐Air CO 2 Enrichment experiment, located at Horsham, Australia. Treatments included CO 2 by water, N and temperature. The location represents a semi‐arid environment with a seasonal VPD of around 0.5 kPa. Over 3 years, the observed mean biomass at anthesis and grain yield ranged from 4200 to 10 200 kg ha−1 and 1600 to 3900 kg ha−1, respectively, over various sowing times and irrigation regimes. The mean observed response to daytime eCO 2 (from 365 to 550 μmol mol−1 CO 2) was relatively consistent for biomass at stem elongation and at anthesis and LAI at anthesis and grain yield with 21%, 23%, 21% and 26%, respectively. Seasonal water use was decreased from 320 to 301 mm (P = 0.10) by eCO 2, increasing water use efficiency for biomass and yield, 36% and 31%, respectively. The performance of six models (APSIM‐Wheat, APSIM‐Nwheat, CAT‐Wheat, CROPSYST, OLEARY‐CONNOR and SALUS) in simulating crop responses to eCO 2 was similar and within or close to the experimental error for accumulated biomass, yield and water use response, despite some variations in early growth and LAI. The primary mechanism of biomass accumulation via radiation use efficiency (RUE) or transpiration efficiency (TE) was not critical to define the overall response to eCO 2. However, under irrigation, the effect of late sowing on response to eCO 2 to biomass accumulation at DC65 was substantial in the observed data (~40%), but the simulated response was smaller, ranging from 17% to 28%. Simulated response from all six models under no water or nitrogen stress showed similar response to eCO 2 under irrigation, but the differences compared to the dryland treatment were small. Further experimental work on the interactive effects of eCO 2, water and temperature is required to resolve these model discrepancies.

A field trial, a lysimeter system study and a nutrient solution experiment were conducted to determine the genotypic differences in nitrogen (N) uptake among wheat (Triticum aestivum L.) genotypes differing in vigour of early growth. Plant growth and N uptake of Vigour 18, a breeding line with early vigour, and the commercial cultivars Westonia, Tincurrin, Camm and Janz were compared. Shoot biomass of Vigour 18 was higher than that of the other genotypes, except for Westonia at booting when 50 kg N ha -1 was applied 3 d after wheat emergence. Vigour 18 had significantly higher efficiency of fertiliser-N uptake than the other four cultivars at tillering when 50 kg N ha -1 was applied. Fertiliser-N uptake efficiency at booting was similar in Vigour 18 and Westonia, but significantly higher than in three other commercial cultivars. Vigour 18 had higher root dry matter, root-length density and root surface area than Janz when examined in columns of soil. The greater root growth of Vigour 18 occurred across all soil layers to a depth of 0.6 m. Differences in total N uptake between Vigour 18 and Janz were apparent from tillering (Z14,22) to booting (Z19,24,49). Vigour 18 also had significantly higher shoot biomass and N uptake than Janz when grown in nutrient culture. Nitrate reductase activity (NRA) expressed on a whole-plant basis was higher for Vigour 18 than for Janz, and was related to total N uptake. However, NRA expressed on a perunit-fresh-weight basis was not significantly different across the cultivars tested. It is concluded that vigorous early root and shoot growth in Vigour 18 was the main driving force for higher N uptake.