Both within and between species, leaves of plants display wide ranges in structural features. These features include: gross investments of carbon and nitrogen substrates (e.g. leaf mass per unit area); stomatal density, distribution between adaxial and abaxial surfaces, and aperture; internal and external optical scattering structures; defensive structures, such as trichomes and spines; and defensive compounds, including UV screens, antifeedants, toxins, and silica abrasives. I offer a synthesis of selected publications, including some of my own. A unifying theme is the adaptive value of expressing certain structural features, posed as metabolic costs and benefits, for (1) competitive acquisition and use of abiotic resources (such as water, light and nitrogen) and (2) regulation of biotic interactions, particularly fungal attack and herbivory. Both acclimatory responses in one plant and adaptations over evolutionary time scales are covered where possible. The ubiquity of trade-offs in function is a recurrent theme; this helps to explain diversity in solutions to the same environmental challenges but poses problems for investigators to uncover numerous important trade-offs. I offer some suggestions for research, such as on the need for models that integrate biotic and abiotic effects (these must be highly focused), and some speculations, such as on the intensity of selection pressures for these structures.

For three decades, hypotheses relating to the occurrence and function of cyclic nucleotides in higher plants have been highly controversial. Although cyclic nucleotides had been shown to have key regulatory roles in animals and bacteria, investigations with higher plants in the 1970s and early 1980s were criticized on the basis of (i) a lack of specificity of effects apparently elicited by cyclic nucleotides, (ii) the equivocal identification of putative endogenous cyclic nucleotides and (iii) ambiguity in the identification of enzymes connected with cyclic nucleotide. More recent evidence based on more rigorous identification procedures has demonstrated conclusively the presence of cyclic nucleotides, nucleotidyl cyclases and cyclic nucleotide phosphodiesterases in higher plants, and has identified plant processes subject to regulation by cyclic nucleotides. Here we review the history of the debate, the recent evidence establishing the presence of these compounds and their role; future research objectives are discussed.

Summary 221

I. Introduction 221

1. The role of sucrose in plants 221

2. C4photosynthesis 222

II. Pathway of sucrose synthesis in C4plants 223

III. Control of sucrose synthesis in C4plants 225

1. The diurnal cycle in C3plants 225

2. The diurnal cycle in C4plants 227

3. Abiotic stress and sucrose synthesis 230

4. Integration of sucrose synthesis with other metabolic pathways 232

IV. Future prospects 233

Acknowledgements 234

References 234

Sucrose has a central role in the metabolism of all higher plants. Here we discuss the location of sucrose synthesis in the leaves of C4 plants, the control of flux through the pathway and its response to environmental conditions, and finally some of the prospects for the genetic manipulation of sucrose metabolism in C4 plants. Much of our knowledge about sucrose synthesis in plants comes from C3 species; it is evident, from those studies of C4 species that are available, that there are many similarities between sucrose synthesis in C3 and C4 plants. However, some of the basic regulatory mechanisms common to both C3 and C4 plants seem to have been adapted for the specialized photosynthetic metabolism of C4 plants. There are also some other important differences: for example, some C4 species possess photosynthetic cells with little or no capacity for sucrose synthesis. For these reasons it is not always appropriate to extrapolate directly from C3 to C4 plants. Even where data are available from one C4 species, usually maize, it should not be assumed that all C4 plants are necessarily the same in every respect. Although C4 plants constitute a small fraction of the plant kingdom as a whole, they include a disproportionate number of agriculturally important species. C4 plants also have some advantages over C3 plants for studies of the regulation of cell-specific gene expression and the control of metabolism. For these reasons we suggest that they are worthy of more attention by researchers.

The mechanical behaviour of large foliage leaves in response to static and dynamic mechanical forces is reviewed in the context of a few basic engineering principles and illustrated in terms of species drawn from a variety of vascular plant lineages. When loaded under their own weight or subjected to externally applied forces, petioles simultaneously bend and twist, and thus mechanically operate as cantilevered beams. The stresses that develop in petioles reach their maximum intensities either at their surface or very near their centroid axes, where they are accommodated either by living and hydrostatic tissues (parenchyma and collenchyma) or dead and stiff tissues (sclerenchyma and vascular fibres) depending on the size of the leaf and the species from which it is drawn. Allometric analyses of diverse species indicate size-dependent variations in petiole length, transverse shape, geometry and stiffness that accord well with those required to maintain a uniform tip-deflection for leaves with laminae differing in mass. When dynamically loaded, the laminae of many broad-leaved species fold and curl into streamlined objects, thereby reducing the drag forces that they experience and transmit to their subtending petioles and stems. From a mechanical perspective, the laminae of these species operate as stress-skin panels that distribute point loads more or less equally over their entire surface. Although comparatively little is known about the mechanical structure and behaviour of foliage leaves, new advances in engineering theory and computer analyses reveal these organs to be far more complex than previously thought. For example, finite-element analyses of the base of palm leaves reveal that stresses are decreased when these structures are composed of anisotropic as opposed to isotropic materials (tissues).

Leaf expansion rate varies with leaf temperature, photon flux density (PPFD), evaporative demand and soil water status. In most simulation models, it is calculated every day by multiplying the amount of carbohydrate available to leaves by specific leaf area (SLA). However, leaf expansion rate is considerably reduced by mild water deficits which do not affect photosynthesis, and is not affected by a reduction in the PPFD intercepted during rapid leaf expansion. Specific leaf area undergoes a several-fold variability depending on PPFD, soil water status and time of day. It is increased when environmental conditions have a greater depressive effect on expansion rate than on photosynthesis, and is decreased in the opposite case. It is therefore appropriate to model leaf expansion independently of the plant carbon budget. Consistent characteristics can be deduced from a series of experiments, allowing a model of leaf expansion to be proposed. (i) Time courses of relative leaf expansion rate and of epidermal cell division rate are well conserved within a plant and across a large range of environmental conditions, provided that durations and rates are expressed in thermal time. Maximum relative rates are common to all zones of a leaf and to all leaves of a plant, in maize and sunflower. (ii) A water deficit, or a reduction in intercepted PPFD, imposed in the first half of the period of leaf development affects the relative expansion rate in the deficit only, but permanently affects the absolute expansion rate. In contrast, a reduction in PPFD causes no effect on leaf expansion if imposed in the rapid expansion period when the leaf is autotrophic. (iii) Expansion rate is related to evaporative demand and to the concentration of ABA in the xylem sap with relationships that apply under both field and laboratory conditions. (iv) Tissue expansion and epidermal cell division behave as independent processes which determine epidermal cell area at each time.

We have explored the relationships between specific leaf area calculated for a whole plant and its individual leaves. Barley was grown in hydroponics in controlled environment cabinets. Plants were harvested on the basis of physiological age (defined as the number of days after full expansion of leaves on the main stem) and the area and weight of whole, fully expanded, leaves measured and specific leaf area (SLA) of individual leaves or whole plants calculated. Specific leaf area calculated for individual leaves (SLAL) varied with leaf position and with leaf age after full expansion whereas SLA calculated for whole plants (SLAP) varied with plant age. The same conclusions were reached whether the results were based on total dry weight or dry weight minus soluble carbohydrates (‘structural weight’). Transferring plants to shade on the day of full expansion of the third leaf on the main stem increased the SLAP, and also SLAL of leaves 3 and 4 on the main stem (leaf 4 being the younger leaf of the two), because of a decrease in the ‘structural weight’ of these leaves. However SLAL of leaf 2 (which was older than leaf 3) was not affected by shading; the effect was confined to leaves developing in the new conditions.

The contribution of the starch and soluble carbohydrate pools to the diurnal variations of leaf mass per unit area (LMA) has been investigated in tomato leaves. A glasshouse experiment was carried out with plants pruned to two or five fruits per truss. Leaflets were sampled at sunrise, noon and sunset at different positions within the leaf (basal or terminal), and on different sympods along the stem. Carbohydrate contents and LMA were significantly higher in the terminal than in the basal leaflets, except at sunrise. During the day, differences in starch accumulation between terminal and basal leaflets increased with leaf height on the plant. Among sympods, the soluble carbohydrate content of the terminal leaflets did not vary significantly, whereas at 13.00 h the LMA was minimum in the middle of the plant and maximum at the top, and the leaf starch content significantly increased half-way up the plant. The plant fruit load had only small and non-significant effects on the LMA and carbohydrate contents. The response of LMA and carbohydrate contents to changing source activity was observed under controlled climatic conditions. The starch pool of fully expanded leaves was rapidly filled and emptied under increasing and decreasing source activity. In young expanding leaves, this pool was hardly filled during daylight. On average the soluble carbohydrates did not contribute significantly to the diurnal variations in LMA, whereas fluctuations in starch explained c. 70% and 44% of these variations in the upper and lower leaves, respectively. The results are discussed with respect to the modelling of LMA at the level of individual tomato leaves or sympods.

The tissue-specific and developmental expression of histone 2A was studied in onion (Allium cepa ‘Robusta’), using northern blots. Histone 2A expression was enriched in basal tissues, particularly in the inner, meristematically active parts of bulbs. The expression was assessed during a time course of bulb development, dormancy onset and post-harvest sprouting in field-grown material. During bulb development histone 2A expression in the inner bulb declined rapidly during bulb ripening, reaching a minimum with the onset of dormancy. During post-harvest storage, expression increased slowly, reaching a peak in the spring, coinciding with the first observed sprout emergence. It was concluded that in onion, as in other plant systems, histone 2A expression is linked to cell division and dormancy level, the peak in expression during post-harvest storage indicating the time of dormancy breakage. In cultivars where post-harvest sprouting occurred much earlier or much later than in ‘Robusta’, this expression peak occurred at about the same time of year, regardless of sprouting time. It was concluded that differences in storage longevity between cultivars were not due to differing times of dormancy breakage. Factors controlling the rate of sprout emergence post-dormancy are likely to be major determinants of storage capacity.

The aim of this study was to investigate whether genetically different pollen donors (Betula pendula clones) differed in pollen-tube growth rate across 11 maternal plants and in vitro, and whether the differences between the donors were consistent across the recipients. To compare the seed-siring success of competing pollen donors, a two-donor hand-pollination experiment with six donors and six recipients was conducted. The experiments were performed at a plastic-house seed orchard. The donors showed significant variation in pollen-tube growth rate on all the 11 recipients. The rankings of the pollen donors were statistically consistent across different maternal plants. A significant positive correlation between pollen tube growth in vivo and in vitro was found. The seed-siring success of two competing pollen donors was unequal in 20 of 29 cases and there was a significant positive correlation between seed-siring success and pollen-tube growth rate in vivo and in vitro. The results show that fertilizations are not random and pollen competition operates in a B. pendula seed orchard population.

The composition and morphology of leaves exposed to elevated [CO2] usually change so that the leaf nitrogen (N) per unit dry mass decreases and the leaf dry mass per unit area increases. However, at ambient [CO2], leaves with a high leaf dry mass per unit area usually have low leaf N per unit dry mass. Whether the changes in leaf properties induced by elevated [CO2] follow the same overall pattern as that at ambient [CO2] has not previously been addressed. Here we address this issue by using leaf measurements made at ambient [CO2] to develop an empirical model of the composition and morphology of leaves. Predictions from that model are then compared with a global database of leaf measurements made at ambient [CO2]. Those predictions are also compared with measurements showing the impact of elevated [CO2]. In the empirical model both the leaf dry mass and liquid mass per unit area are positively correlated with leaf thickness, whereas the mass of C per unit dry mass and the mass of N per unit liquid mass are constant. Consequently, both the N[ratio ]C ratio and the surface area[ratio ]volume ratio of leaves are positively correlated with the liquid content. Predictions from that model were consistent with measurements of leaf properties made at ambient [CO2] from around the world. The changes induced by elevated [CO2] follow the same overall trajectory. It is concluded that elevated [CO2] enhances the rate at which dry matter is accumulated but the overall trajectory of leaf development is conserved.

Genotypic variability was studied in two Mediterranean grass species, Bromus erectus and Dactylis glomerata, with regard to the response to CO2 of leaf total non-structural carbohydrate concentration ([TNC]lf), specific leaf area (SLA), and leaf carbon and nitrogen concentrations ([C]lf and [N]lf, respectively). Fourteen genotypes of each species were grown together on intact soil monoliths at ambient and elevated CO2 concentrations (350 and 700 μmol mol−1, respectively). In both species, the most consistent effect of elevated CO2 was an increase in [TNC]lf and a decrease in leaf nitrogen concentration when expressed either as total dry mass [Nm]lf, structural dry mass [Nmst]lf or leaf area [Na]lf. The SLA decreased only in D. glomerata, due to an accumulation of total non-structural carbohydrates and to an increase in leaf density. No genotypic variability was found for any variable in B. erectus, suggesting that genotypes responded in a similar way to elevated CO2. In D. glomerata, a genotypic variability was found only for [Cst], [Nm]lf, [Nmst]lf and [Na]lf. Since [Nm]lf is related to plant growth and is a strong determinant of plant–herbivore interactions, our results suggest evolutionary consequences of elevated CO2 through competitive interactions or herbivory.

The resurrection plant Myrothamnus flabellifolia has the ability to recover from repeated prolonged and extreme desiccation cycles. During the dry state the inner walls of the xylem vessels seemed to be covered, at least partly, by a lipid film as shown by Sudan III and Nile Red staining. The lipid film apparently functioned as an ‘internal cuticle’ which prevented the adjacent parenchyma ray cells from complete water loss. The hydrophobic nature of the inner xylem walls was supported by the finding that benzene ascended as rapidly as water in the xylem of dry Myrothamnus branches. On watering, numerous lipid bodies were found in the water-conducting vessels, presumably formed from the lipid film and/or from lipids excreted from the adjacent living cells into the vessels. The presence of lipid bodies within the vessels, as well as the hydrophobic properties of the inner xylem walls, could explain the finding that the xylem pressure of hydrated, well watered plants (measured both under laboratory and field conditions with the xylem pressure probe) never dropped below c. −0.3 MPa and that cavitation occurred frequently at low negative xylem pressure values (−0.05 to −0.15 MPa). The xylem pressure of M. flabellifolia responded rapidly and strongly to changes in relative humidity and temperature, but less obviously to changes in irradiance (which varied between 10 and c. 4000 μmol m m−2 s−1). The morphological position of the stomata in the leaves could explain the extremely weak and slow response of the xylem pressure of this resurrection plant to illumination changes. Stomata were most abundant in the furrows, and were thus protected from direct sunlight. Simultaneous measurements of the cell turgor pressure in the leaf epidermal cells (made by using the cell turgor pressure probe) revealed that the xylem and the cell turgor pressure dropped in a ratio of 1:0.7 on changes in the environmental parameters, indicating a quite close hydraulic connection and, thus, water equilibrium between the xylem and cellular compartments. An increase in irradiance of c. 700 μmol m−2 s−1 resulted in a turgor pressure decrease from 0.63 to 0.48 MPa. Correspondingly, the cell osmotic pressure increased from 1.03 to 1.22 MPa. From these values and by assuming water equilibrium, the osmotic pressure of the xylem sap was estimated to be 0.25–0.4 MPa. This value seems to be fairly high but may, however, be explained by the reduction of the water volume within the vessels due to the floating lipid bodies.