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Stressful episodic weather is likely to affect the C balance of trees as the climate changes, potentially altering survival. However, the role of elevated CO2 concentration ([CO2]) in tolerating off-season episodic extremes is not clear. We tested for interactive effects of elevated CO2 and springtime heat stress on photosynthesis for seven genotypes of Eucalyptus camaldulensis Dehnh. var. camaldulensis, representing its widespread distribution across south-eastern Australia. We grew clonal material under glasshouse conditions of ambient (aCO2; 400 parts per million (ppm)) or elevated (eCO2; 640ppm) [CO2], and air temperatures of 25:17°C (day:night), and measured the electron transport rate in PSII (ETR), stomatal conductance to water vapour (gs) and net CO2 assimilation (A). Measurements were made before, during and after a four-day temperature excursion of 35:27°C. ETR and A were ~17% higher for plants grown in eCO2 than in aCO2. Photosynthesis remained stable for plants in eCO2 during the heatwave. Based on the effect size ratio (eCO2:aCO2), gs and ETR were temporarily affected more by the heatwave than A. A reduction in ETR in eCO2 was the only lasting effect of the heatwave. There were no significant differences among genotypes. Correlations between photosynthesis and climate of origin differed for plants grown in aCO2 compared with eCO2, suggesting potential complex and multiple control points on photosynthesis.

Circadian resonance, whereby a plant's endogenous rhythms are tuned to match environmental cues, has been repeatedly shown to be adaptive, although the underlying mechanisms remain elusive. Concomitantly, the adaptive value of nocturnal transpiration in C3 plants remains unknown because it occurs without carbon assimilation. These seemingly unrelated processes are interconnected because circadian regulation drives temporal patterns in nocturnal stomatal conductance, with maximum values occurring immediately before dawn for many species. We grew individuals of six Eucalyptus camaldulensis genotypes in naturally lit glasshouses and measured sunset, predawn and midday leaf gas exchange and whole-plant biomass production. We tested whether sunrise anticipation by the circadian clock and subsequent increases in genotype predawn stomatal conductance led to rapid stomatal opening upon illumination, ultimately affecting genotype differences in carbon assimilation and growth. We observed faster stomatal responses to light inputs at sunrise in genotypes with higher predawn stomatal conductance. Moreover, early morning and midday stomatal conductance and carbon assimilation, leaf area and total plant biomass were all positively correlated with predawn stomatal conductance across genotypes. Our results lead to the novel hypothesis that genotypic variation in the circadian-regulated capacity to anticipate sunrise could be an important factor underlying intraspecific variation in tree growth.