Roelof Oomen

Abstract Questions Plant communities fulfil key functions in the ecosystem, which can be characterized by their plant functional traits. In functional ecology, plant communities are considered to hold a set of trait attributes reflecting a specific plant strategy adapted to persist in the environment to which they are exposed. In semi‐arid grasslands of the R epublic of S outh A frica, we addressed the following questions: how are community‐aggregated plant functional traits ( CPFT ) shaped by grazing gradients; which plant strategies are associated with the response of CPFT s; and are environmental factors, such as soil properties and grazing management, interrelated with the functional response of vegetation to grazing gradients? Location Semi‐arid grasslands close to T haba N chu, F ree S tate ( R epublic of S outh A frica). Methods Piosphere transects from a water point into the field were established to portray grazing gradients on two communal grazing areas with continuous grazing and two commercial farms with rotational grazing. Along each transect, six plots (5 × 5 m) were evenly distributed. The trait–transect sampling was applied to record 12 CPFT related to light capture and forage quality. A redundancy analysis was performed to derive relationship between CPFT s, grazing gradients and environmental conditions. Results Grazing intensity decreased along piosphere transects, from the water point into the field. Most CPFT s responded to this decreasing gradient of grazing intensity and so allowed derivation of trait syndromes that clearly reflect plant strategies of ruderal and competitive vegetation. Close to water points, plants had higher nitrogen concentrations, fewer cell wall components and higher specific leaf area, hence light capture might be faster and more efficient per leaf area and leaf mass. Plant communities exposed to intensive grazing were well adapted to defoliation, trampling and nutrient accumulation through fast growth rates and a quick return strategy. Conclusions In the sacrifice zone around water points, there is an ecological niche for vegetation communities exhibiting a strategy of fast growth, which is well adapted to intense and frequent grazing and is also associated with forage of high nutritional quality.

BACKGROUND AND AIMS: Crown structure and above-ground biomass investment was studied in relation to light interception of trees and lianas growing in a 6-month-old regenerating forest. METHODS: The vertical distribution of total above-ground biomass, height, diameter, stem density, leaf angles and crown depth were measured for individual plants of three short-lived pioneers (SLPs), four long-lived pioneers (LLPs) and three lianas. Daily light interception per individual Phi(d) was calculated with a canopy model. The model was then used to estimate light interception per unit of leaf mass (Phi(leaf mass)), total above-ground mass (Phi(mass)) and crown structure efficiency (E(a), the ratio of absorbed vs. available light). KEY RESULTS: The SLPs Trema and Ochroma intercepted higher amounts of light per unit leaf mass (Phi(leaf mass)) because they had shallower crowns, resulting in higher crown use efficiency (E(a)) than the other species. These SLPs (but not Cecropia) were also taller and intercepted more light per unit leaf area (Phi(area)). LLPs and lianas had considerably higher amounts of leaf mass and area per unit above-ground mass (LMR and LAR, respectively) and thus attained Phi(mass) values similar to the SLPs (Phi(mass)=Phi(area)xLAR). Lianas, which were mostly self-supporting, had light interception efficiencies similar to those of the trees. CONCLUSIONS: These results show how, due to the trade-off between crown structure and biomass allocation, SLPs, and LLPs and lianas intercept similar amount of light per unit mass which may contribute to the ability of the latter two groups to persist.

We related above-ground biomass allocation to light interception by trees and lianas growing in three tropical rain forest stands that were 0.5, 2 and 3-year-old regeneration stages after slash and burn agriculture. Stem height and diameter, leaf angle, the vertical distribution of total above-ground biomass and leaf longevity were measured in individuals of three short-lived pioneers (SLP), four later successional species (LS) and three lianas (L). Daily light capture per individual (¿d) was calculated with a canopy model. Mean daily light interception per unit leaf area (¿area), leaf mass (¿leaf mass) and above-ground mass (¿mass) were used as measures of instantaneous efficiency of biomass use for light capture. With increasing stand age, vegetation height and leaf area index increased while light at the forest floor declined from 34 to 5%. The SLP, Trema micanthra and Ochroma pyramidale, dominated the canopy early in succession and became three times taller than the other species. SLP had lower leaf mass fractions and leaf area ratios than the other groups and this difference increased with stand age. Over time, the SLP intercepted increasingly more light per unit leaf mass than the other species. Lianas, which in the earliest stage were self-supporting and started climbing later on, gradually became taller at a given mass and diameter than the trees. Yet, they were not more efficient than trees in light interception. SLP had at least three-fold shorter leaf life spans than LS and lianas. Consequently, total light interception calculated over the mean life span of leaves (¿leaf mass total = ¿area × SLAdeath leaves× leaf longevity) was considerably lower for the SLP than for the other groups. Synthesis. We suggest that early dominance in secondary forest is associated with a high rate of leaf turnover which in turn causes inefficient long-term use of biomass for light capture, whereas persistence in the shade is associated with long leaf life spans. This analysis shows how inherent tradeoffs in crown and leaf traits drive long-term competition for light, and it presents a conceptual tool to explain why early dominants are not also the long-term dominants.