Mineral nutrition and growth of tropical maize as affected by soil acidity

Soil constraints linked to low pH reduce grain yield in about 10% of the maize growing area in tropical developing countries. The aim of this research was to elucidate the reasons for this maize yield reduction on an oxisol of Guadeloupe. The field experiment had two treatments: the native non-limed soil (NLI, pH 4.5, 2.1 cmol Al kg^–1, corresponding to 20% Al saturation), and the same soil limed 6 years prior to the experiment (LI, pH 5.3, 0 cmol Al kg^–1). The soils were fertilized with P and N. The above-ground biomass, root biomass at flowering, grain yield and yield components, leaf area index (LAI), light interception, radiation-use-efficiency (RUE), P and N uptake, soil water storage, and soil mineral N were measured during the maize cycle. The allometric relationships between shoot N concentration, LAI and above-ground biomass in LI were similar to those reported for maize cropped in temperate regions, indicating that these relationships are also useful to describe maize growth on tropical soils without Al toxicity. In NLI, soil acidity severely affected leaf appearance, leaf size and consequently the LAI, which was reduced by 60% at flowering, although the RUE was not affected. Therefore, the reduction in the above-ground biomass (30% at flowering) and grain yield (47%) were due to the lower LAI and light interception. At flowering, the root/shoot ratio was 0.25 in NLI and 0.17 in LI, and the root biomass in NLI was reduced by 64% compared to LI. Nitrogen uptake was also reduced in NLI in spite of high soil N availability. Nevertheless, shoot N concentration vs aboveground biomass showed a typical decline in both treatments. In NLI, the shoot P concentration vs above-ground biomass relationship showed an increase in the early stages, indicating that P uptake and root-shoot competition for the absorbed P in the early plant stages controlled the establishment and the development of the leaf area.     

Seasonal patterns in water use and leaf turnover of different plant functional types in a species-rich woodland,south-western Australia

Woodlands in south-western Australia are evergreen and transpire throughout the year despite the long, hot and dry summers of the Mediterranean climate. Results from a case study in a species-rich Banksia woodland are used to discuss the ecological and physiological properties that appear to be essential features of this and similar communities. Tree, shrub and perennial herbaceous species with long-lived leaves dominate the community, whereas winter-green herbaceous species with short-lived leaves constitute a minor group. The total leaf area index is therefore reasonably constant in all seasons. Leaf area index is low and canopies are open, causing good coupling between the vegetation and the atmosphere, and making stomatal control an effective regulator of transpiration. Mean maximum (winter) stomatal conductances were high at approximately 300 mmol m^–2 s^–1. Deep-rootedness allows the dominant species to access soil moisture throughout the unsaturated zone, and down to the capillary fringe of the saturated zone. Shrubs and herbs with shallow roots experience greater drought stress during summer. Rates of community evapotranspiration are limited by leaf area index in the wet season, and further reduced by stomatal closure in the dry season. Deep-rooted plants appear to decrease their stomatal conductance before the development of severe drought stress. Such conservative behaviour, possibly related to plant hydraulic constraints, is a contributing factor to the limited seasonality in community water use.     

Soil type affects nitrogen conservation in foliage of small Pinus sylvestris L. trees

Nutrient conservation in plants and soil fertility may be intricately linked. We studied nitrogen conservation in small Scots pine (Pinus sylvestrisL.) trees growing in stands on organogenic Dystric Histosols and on mineral Podzols. Nitrogen-resorption efficiency (NRE) and proficiency (NRP) of senescent needles, and mean residence time of nitrogen (MRT) were studied in relation to needle surface area, needle longevity, and leaf mass per area (LMA). Trees on Podzols had higher nitrogen concentration in green needles than the trees on Dystric Histosols, but the nitrogen concentration of yellowing needles was similar for trees on both soil types. NRE averaged 65±3.5% (mean±SD) and 56±7.2% for the trees on Podzols and Dystric Histosols, respectively. Neither NRP (0.44±0.05% and 0.35±0.07%, respectively) nor MRT (8.4±2.3 and 6.1±1.2 years) differed significantly between the stands on the two soil types. Mean needle surface area was significantly smaller in trees on Dystric Histosols (76±29 mm²) than on Podzols (131±38 mm²), whereas needle longevity varied between 2 and 4 years independently of the soil type. Trees invested, on average, the same amount of dry matter per unit of needle area on both soil types. Growth of trees, measured as increment of shoot length, was more restricted on Dystric Histosols (55±18 mm yr^–1) than on Podzols (184±44 mm yr^–1). The results of the correlation analysis applied to pooled data were inconsistent with the relations between traits of stress resistance syndrome observed in inter-specific comparisons. The study indicated that Scots pine trees relocated nitrogen from senescent foliage more efficiently on mineral Podzols than on organogenic Dystric Histosols, but the minimum nitrogen concentration of needles appeared to be similar on both soil types.     

Does the photosynthetic light‐acclimation need change in leaf anatomy?

There is a strong correlation between leaf thickness and the light‐saturated rate of photosynthesis per unit leaf area (P_max). However, when leaves are exposed to higher light intensities after maturation, P_max often increases without increasing leaf thickness. To elucidate the mechanism with which mature leaves increase P_max, the change in anatomical and physiological characteristics of mature leaves of Chenopodium album, which was transferred from low to high light condition, were examined. When compared with leaves subjected to low light continuously (LL leaves), the leaves transferred from low to high light (LH leaves) significantly increased P_max. The transfer also increased the area of chloroplasts facing the intercellular space (S_c) and maintained a strong correlation between P_max and S_c. The mesophyll cells of LL leaves had open spaces along cell walls where chloroplasts were absent, which enabled the leaves to increase P_max when they were exposed to high light (LH). However, the LH leaves were not thick enough to allow further increase in P_max to the level in HH leaves. Thus leaf thickness determines an upper limit of P_max of leaves subjected to a change from low to high light conditions. Shade leaves would only increase P_max when they have open space to accommodate chloroplasts which elongate after light conditions improve.     

Ethylene is required in tobacco to successfully compete with proximate neighbours

Plants sense neighbours even before these cause a decrease in photosynthetic light availability. Light reflected by proximate neighbours signals a plant to adjust growth and development, in order to avoid suppression by neighbour plants. These phenotypic changes are known as the shade‐avoidance syndrome and include enhanced shoot elongation and more upright‐positioned leaves. In the present study it was shown that these shade‐avoidance traits in tobacco (Nicotiana tabacum) are also induced by low concentrations of ethylene. Furthermore, it was shown that transgenic plants, insensitive to ethylene, have a delayed appearance of shade‐avoidance traits. The increase in both leaf angles and stem elongation in response to neighbours are delayed in ethylene‐insensitive plants. These data show that ethylene is an important component in the regulation of neighbour‐induced, shade‐avoidance responses. Consequently, ethylene‐insensitive plants lose competition with wild‐type neighbours, demonstrating that sensing of ethylene is required for a plant to successfully compete for light.