H igh temperature stress is an important yield limiting factor in both spring and winter wheat (Triticum aestivum L.). At the present rates of greenhouse gas emissions and population growth, it is expected that mean surface air temperatures will increase in the range of 1.8 to 5.8°C by the end of this century (Intergovernmental Panel on Climate Change, 2007). It is predicted that future climates will not only be associated with an increase in mean temperatures (Easterling et al., 1997) but also with an increase in the frequency of episodes of high temperatures . In addition, climate models foresee that there will be a relatively greater increase in nighttime temperatures as compared to daytime temperatures. Over the past century global daily minimum temperatures increased more than twice compared to increases in daily maximum temperatures (Easterling et al., 1997). Recent studies have shown that historical yields of rice (Oryza sativa L.; Peng et al., 2004) and wheat (Lobell et al., 2005) were strongly correlated with minimum (nighttime) temperatures, rather than daytime maximum temperatures. Decreasing rice yields in the Philippines were related to increasing nighttime temperatures (Peng et al., 2004), and increasing wheat yields in Mexico were related to decreasing nighttime temperatures (Lobell et al., 2005). ABSTRACTClimate models predict greater increases in nighttime temperature in the future. The impacts of high nighttime temperature on wheat (Triticum aestivum L.) are not well understood. Objectives of this research were to quantify the impact of high nighttime temperatures during reproductive development on phenology, physiological, vegetative, and yield traits of wheat. Two spring wheat cultivars (Pavon-76 and Seri-82) were grown at optimum temperatures (day/night, 24/14°C; 16/8 h light/dark photoperiod) from sowing to booting. Thereafter, plants were exposed to four different nighttime temperatures (14, 17, 20, 23°C) until maturity. The daytime temperature was 24°C across all treatments. There were signifi cant infl uences of high nighttime temperatures on physiological, growth, and yield traits, but no cultivar or cultivar by temperature interactions were observed. High nighttime temperatures (>14°C) decreased photosynthesis after 14 d of stress. Grain yields linearly decreased with increasing nighttime temperatures, leading to lower harvest indices at 20 and 23°C. High nighttime temperature (≥20°C) decreased spikelet fertility, grains per spike, and grain size. Compared to the control (14°C), grain fi lling duration was decreased by 3 and 7 d at night temperatures of 20 and 23°C, respectively. High nighttime temperature increased the expression of chloroplast protein synthesis elongation factor in both cultivars suggesting possible involvement of this protein in plant response to stress.

High temperature and drought stress are among the two most important environmental factors influencing crop growth, development and yield processes. These two stresses commonly occur in combination. Objectives of this research were to investigate the independent and combined effects of high temperature and drought stress during grain filling on physiological, vegetative and yield traits and expression of a chloroplast protein synthesis elongation factor (EF‐Tu) of wheat (Triticum aestivum L.). Two spring wheat cultivars (Pavon‐76 and Seri‐82) were grown at control temperatures (CT; day/night, 24/14 °C; 16/8 h photo/dark period) from sowing to heading. Thereafter, one half of the plants were exposed to high temperature stress (HT; 31/18 °C in Exp. 1 and 34/22 °C in Exp. 2), drought stress (withholding water), or a combination of both HT and drought stress. There were significant influences of HT and/or drought stress on physiological, growth and yield traits. There was no cultivar or cultivar by temperature or cultivar by drought interaction effects on most traits. The decreases in leaf photosynthesis were greater at HT compared with drought alone throughout the stress period, and the combination of HT and drought had the lowest leaf photosynthetic rates. Overall, HT or drought had similar effects (about 48–56 % decrease) on spikelet fertility, grain numbers and grain yield. High temperature decreased grain numbers (by 56 % averaged across both experiments) and individual grain weight (by 25 %), while, respective decreases due to drought were 48 % and 35 %. This suggests that the grain numbers were more sensitive to HT and grain weights to drought for the range of temperatures tested in this research. The interaction between HT and drought stress was significant for total dry weights, harvest index and spikelet fertility, particularly when HT stress was severe (34/22 °C). The combined effects of HT and drought were greater than additive effects of HT or drought alone for leaf chlorophyll content, grain numbers and harvest index. High temperature stress and the combination of HT and drought stress but not drought stress alone resulted in the overexpression of EF‐Tu in both spring wheat cultivars.

Sorghum (Sorghum bicolor L. Moench) grown in semiarid regions is often exposed to short periods of high‐temperature (HT) stress during reproductive development. Objectives of this research were (i) to quantify the effects of short episodes of HT stress during reproductive development on physiological, growth, and yield processes of grain sorghum and (ii) to identify the stage(s) most sensitive during the reproductive development phase to HT stress. Plants of hybrid DK‐28 E were grown in growth chambers at daytime maximum/nighttime minimum optimum temperature (OT) of 32/22°C until 29 d after sowing. Thereafter, plants were exposed to OT or HT (40/30°C) or were reciprocally transferred at 10‐d intervals (10 d before flowering, 0, 10, 20, and 30 d after flowering [DAF]) from OT to HT and vice versa. Transferred plants remained in the new temperature regime for 10 d before being returned to their original temperature regime. Continuous HT stress delayed panicle emergence and decreased plant height, seed set, seed numbers, seed yield, seed size, and harvest indices but did not influence leaf photosynthesis. Exposure to short (10‐d) periods of HT stress at flowering and 10 d before flowering caused maximum decreases in seed set and seed yield, and HT stress during postflowering stages (10, 20, and 30 DAF) decreased seed yield, with a larger reduction at early stages of seed development.