Sex-related differences in reproductive effort can lead to differences in vegetative growth and stress tolerance. However, do all dioecious plants show sex-related differences in stress tolerance? To what extent can the environmental context and modularity mask sex-related differences in stress tolerance? Finally, to what extent can physiological measurements help us understand secondary sexual dimorphism? This opinion paper aims to answer these three basic questions with special emphasis on developments in research in this area over the last decade. Compelling evidence indicates that dimorphic species do not always show differences in stress tolerance between sexes; and when sex-related differences do occur, they seem to be highly species-specific, with greater stress tolerance in females than males in some species, and the opposite in others. The causes of such sex-related species-specific differences are still poorly understood, and more physiological studies and diversity of plant species that allow comparative analyses are needed. Furthermore, studies performed thus far demonstrate that the expression of dioecy can lead to sex-related differences in physiological traits-from leaf gas exchange to gene expression-but the biological significance of modularity and sectoriality governing such differences has been poorly investigated. Future studies that consider the importance of modularity and sectoriality are essential for unravelling the mechanisms underlying stress adaptation in male and female plants growing in their natural habitat.

The life cycle of a leaf can be characterized as consisting of different stages: from primordial leaf initiation in the shoot apical meristem (SAM) to leaf senescence. Leaf development, from early leaf growth to senescence, is tightly controlled by plant development and the environment. Here, we primarily focus on summarizing current evidence indicating that photo-oxidative stress occurs at the two extremes of a leaf's lifespan. Some recent studies clearly indicate that--as happens in senescing leaves--emerging new leaves suffer from photo-oxidative stress, which suggests that oxidative stress plays a key role at both ends of the leaf life cycle. We discuss the causes and consequences of suffering from photo-oxidative stress during leaf development, paying attention to the particularities of this process at the two extremes of leaf development. Of particular importance is the current evidence showing mechanisms that maintain an adequate cellular reactive oxygen species/antioxidant (redox) balance that allows growth and prevents oxidative damage in young emerging leaves, while later on photo-oxidative stress induces cell death in senescing leaves. Also of interest is the fact that reductions in the efficiency of photosystem II photochemistry may not necessarily indicate photo-oxidative stress in emerging leaves. In this review, we summarize current knowledge of photoinhibition, photoprotection, and photo-oxidative stress at the two ends of the leaf life cycle: early leaf growth and leaf senescence.

In plants, an individually darkened leaf initiates senescence much more rapidly than a leaf from a whole darkened plant. Combining transcriptomic and metabolomic approaches in Arabidopsis (), we present an overview of the metabolic strategies that are employed in response to different darkening treatments. Under darkened plant conditions, the perception of carbon starvation drove a profound metabolic readjustment in which branched-chain amino acids and potentially monosaccharides released from cell wall loosening became important substrates for maintaining minimal ATP production. Concomitantly, the increased accumulation of amino acids with a high nitrogen-carbon ratio may provide a safety mechanism for the storage of metabolically derived cytotoxic ammonium and a pool of nitrogen for use upon returning to typical growth conditions. Conversely, in individually darkened leaf, the metabolic profiling that followed our C-enrichment assays revealed a temporal and differential exchange of metabolites, including sugars and amino acids, between the darkened leaf and the rest of the plant. This active transport could be the basis for a progressive metabolic shift in the substrates fueling mitochondrial activities, which are central to the catabolic reactions facilitating the retrieval of nutrients from the senescing leaf. We propose a model illustrating the specific metabolic strategies employed by leaves in response to these two darkening treatments, which support either rapid senescence or a strong capacity for survival.

SummaryPlants originating from high altitude have an increased capacity for sucrose accumulation in response to chilling and sucrose content is positively correlated with jasmonic acid in accessions from different altitudes.