Eco-physiology of maize crops under combined stresses.

The yield of maize (Zea mays L.) crops depends on their ability to intercept sunlight throughout the growing cycle, transform this energy into biomass and allocate it to the kernels. Abiotic stresses affect these eco-physiological determinants, reducing crop grain yield below the potential of each environment. Here we analyse the impact of combined abiotic stresses, such as water restriction and nitrogen deficiency or water restriction and elevated temperatures. Crop yield depends on the product of kernel yield per plant and the number of plants per unit soil area, but increasing plant population density imposes a crowding stress that reduces yield per plant, even within the range that maximises crop yield per unit soil area. Therefore, we also analyse the impact of abiotic stresses under different plant densities. We show that the magnitude of the detrimental effects of two combined stresses on field-grown plants can be lower, similar or higher than the sum of the individual stresses. These patterns depend on the timing and intensity of each one of the combined stresses and on the effects of one of the stresses on the status of the resource whose limitation causes the other. The analysis of the eco-physiological determinants of crop yield is useful to guide and prioritise the rapidly progressing studies aimed at understanding the molecular mechanisms underlying plant responses to combined stresses.

Artificial selection for grain yield has increased net CO2 exchange of the ear leaf in maize crops.

Identifying the physiological traits indirectly selected during the search for high-yielding maize hybrids is useful for guiding further improvements. To investigate such traits, in this study we focused on the critical period of kernel formation because kernel number is the main yield component affected by breeding. Our results show that breeding has increased the number of florets per ear and ear growth rate but not the vegetative shoot growth rate, suggesting localised effects around the ear. Consistent with this possibility, breeding has increased the net CO2 exchange of the ear leaf in field-grown crops grown at high population densities. This response is largely accounted for by increased light interception (which increases photosynthesis) and by reduced rates of respiration of the ear leaf in modern hybrids compared to older ones. Modern hybrids show increased ear-leaf area per unit leaf dry matter (specific leaf area), which accounts for the reduced respiratory load per unit leaf area. These observations are consistent with a model where the improved ear leaf CO2 exchange helps the additional florets produced by modern hybrids to survive the critical period of high susceptibility to stress and hence to produce kernels.

Long-Day Photoperiod Enhances Jasmonic Acid-Related Plant Defense.

Agricultural crops are exposed to a range of daylengths, which act as important environmental cues for the control of developmental processes such as flowering. To explore the additional effects of daylength on plant function, we investigated the transcriptome of Arabidopsis (Arabidopsis thaliana) plants grown under short days (SD) and transferred to long days (LD). Compared with that under SD, the LD transcriptome was enriched in genes involved in jasmonic acid-dependent systemic resistance. Many of these genes exhibited impaired expression induction under LD in the phytochrome A (phyA), cryptochrome 1 (cry1), and cry2 triple photoreceptor mutant. Compared with that under SD, LD enhanced plant resistance to the necrotrophic fungus Botrytis cinerea This response was reduced in the phyA cry1 cry2 triple mutant, in the constitutive photomorphogenic1 (cop1) mutant, in the myc2 mutant, and in mutants impaired in DELLA function. Plants grown under SD had an increased nuclear abundance of COP1 and decreased DELLA abundance, the latter of which was dependent on COP1. We conclude that growth under LD enhances plant defense by reducing COP1 activity and enhancing DELLA abundance and MYC2 expression.

The dynamics of FLOWERING LOCUS T expression encodes long-day information.

Long days repeatedly enhance the expression of the FLOWERING LOCUS T (FT) gene during the evening and early night. This signal induces flowering despite low FT expression the rest of the day. To investigate whether this temporal behaviour transmits information, plants of Arabidopsis thaliana were exposed to different day-night cycles, including combinations that induced FT expression out of normal hours. Flowering time best correlated with the integral of FT expression over several days, corrected for a higher evening and early night sensitivity to FT. We generated a system to induce FT expression in a leaf removed 8-12 h later. The expression of flowering genes in the apex and flowering required cycles of induction repeated over several days. Evening and early night FT induction was the most effective. The temporal pattern of FT expression encodes information that discriminates long days from other inputs.

Balancing forces in the photoperiodic control of flowering.

In many plant species, the duration of the daily exposure to light (photoperiod) provides a seasonal cue that helps to adjust flowering time to the most favourable time of the year. In Arabidopsis thaliana, the core mechanism of acceleration of flowering by long days involves the stabilisation of the CONSTANS (CO) protein by light reaching the leaves, the direct induction of the expression of FLOWERING LOCUS T (FT) by CO and the migration of FT to the apex to promote flowering. In rice (Oryza sativa), the promotion of flowering by short days depends on the interplay between light conditions, and the genes Grain number, plant height and heading date locus 7 (Ghd7) and Early heading date 1 (Ehd1). In both cases, other day length-induced changes reinforce the core photoperiodic pathway of promotion of flowering. However, there are regulators of flowering time, quantitatively less important than the core pathways but still significant, which impact in the opposite direction, i.e. favouring rice flowering under long days or Arabidopsis flowering under short days. We show, for instance, that short days enhance leaf expression of SQUAMOSA PROMOTER BINDING PROTEIN-LIKE 3 (SPL3), which stimulates Arabidopsis flowering under these conditions. We propose that fine tuning of flowering time depends on the balance of a hierarchy of multiple points of action of photoperiod on the network controlling flowering.