Search

Tropical lianas deploy most of their leaves towards the top of the forest canopy, whereas trees exhibit a more stratified crown. Forest canopies are often exposed to hot and windy conditions, and how lianas cope with the extremely high transpirational demands under these environments remains unknown. We investigated stem hydraulic properties, leaf drought tolerance, diurnal changes in leaf and stem water potentials (Ψleaf and Ψstem), stomatal conductance (gs), photosynthetic rate, sap flow and stem native percentage loss of conductivity (PLC) for four liana species in a tropical forest in southwest China. Five co-occurring tree species were also selected for comparison. Lianas reached maximal transpiration at a relatively lower vapour pressure deficit (

The savannahs of Asia remain locally unrecognized as distinctive ecosystems, and continue to be viewed as degraded forests or seasonally dry tropical forests. These colonial-era legacies are problematic, because they fail to recognize the unique diversity of Asian savannahs and the critical roles of fire and herbivory in maintaining ecosystem health and diversity. In this review, we show that: the palaeo-historical evidence suggests that the savannahs of Asia have existed for at least 1 million years, long before widespread landscape modification by humans; savannah regions across Asia have levels of C4grass endemism and diversity that are consistent with area-based expectations for non-Asian savannahs; there are at least three distinct Asian savannah communities, namely deciduous broadleaf savannahs, deciduous fine-leafed and spiny savannahs and evergreen pine savannahs, with distinct functional ecologies consistent with fire- and herbivory-driven community assembly. Via an analysis of savannah climate domains on other continents, we map the potential extent of savannahs across Asia. We find that the climates of African savannahs provide the closest analogues for those of Asian deciduous savannahs, but that Asian pine savannahs occur in climates different to any of the savannahs in the southern continents. Finally, we review major threats to the persistence of savannahs in Asia, including the mismanagement of fire and herbivory, alien woody encroachment, afforestation policies and future climate uncertainty associated with the changing Asian monsoon. Research agendas that target these issues are urgently needed to manage and conserve these ecosystems.This article is part of the themed issue ‘Tropical grassy biomes: linking ecology, human use and conservation’.

1. Plant organ biomass partitioning has been hypothesized to be driven by resources, such that species from drier environments allocate more biomass to roots than species from wetter environments to access water at greater soil depths. In savanna systems, fire may select for greater allocation to root biomass, especially in humid environments where fire is more frequent. Therefore, species from drier environments may have been under selection pressure to reach deeper soil water more effectively than species from humid environments, through faster root extension, more efficient depth penetration, and faster plant growth rates to respond rapidly to variable rainfall events. 2. We compared biomass partitioning, root morphology traits [root extension rate, RER; specific taproot length (STRL)] and relative growth rate (RGR) of seedlings of 51 savanna tree species, sampled from three continents (Africa, Australia and South America) in a greenhouse experiment. We used phylogenetically corrected and uncorrected analyses to compare the traits of the groups. We conducted a permanova on the combined traits to establish whether species could be distinguished on the basis of their combined traits. 3. On average, species from humid environments allocated more biomass to roots and less to stems than species from semi-arid environments, consistent with the expectation that fire pressure selects for greater allocation to roots in humid environments. However, some species from humid environments had fast growth rates instead of high allocation to roots. Both RER and STRL were greater among species of semi-arid environments than among species of humid environments, and also differed between continents. Differences between strategies under each climate type appear to be associated with leaf habit. 4. Synthesis. Plant biomass partitioning has been selected by defoliation pressure and the effects of this selection pressure can supersede any selection in response to local water constraints. Root morphological adaptations, but not plant growth rate, of tree seedlings, have been selected in response to water deficits

Rising global demand for natural rubber is expanding monoculture rubber (Hevea brasilensis) at the expense of natural forests in the Old World tropics. Conversion of forests into rubber plantations has a devastating impact on biodiversity and we have yet to identify management strategies that can mitigate this. We determined the life-history traits that best predict bird species occurrence in rubber plantations in SW China and investigated the effects of surrounding forest cover and distance to roads on bird diversity. Mistletoes provide nectar and fruit resources in rubber so we examined mistletoe densities and the relationship with forest cover and rubber tree diameter. In rubber plantations, we recorded less than half of all bird species extant in the surrounding area. Birds with wider habitat breadths and low conservation value had a higher probability of occurrence. Species richness and diversity increased logarithmically with surrounding forest cover, but roads had little effect. Mistletoe density increased exponentially with rubber tree diameters, but was unrelated to forest cover. To maximize bird diversity in rubber-dominated landscapes it is therefore necessary to preserve as much forest as possible, construct roads through plantations and not forest and retain some large rubber trees with mistletoes during crop rotations.

Herbivory contributes substantially to plant functional diversity and in ways that move far beyond direct defence trait patterns, as effective growth strategies under herbivory require modification of multiple functional traits that are indirectly related to defence. In order to understand how herbivory has shaped plant functional diversity, we need to consider the physiology and architecture of the herbivores and how this constrains effective defence strategies. Here we consider herbivory by mammals in savanna communities that range from semi-arid to humid conditions. We posited that the saplings of savanna trees can be grouped into two contrasting defence strategies against mammals, namely architectural defence versus low nutrient defence. We provide a mechanistic explanation for these different strategies based on the fact that plants are under competing selection pressures to limit herbivore damage and outcompete neighbouring plants. Plant competitiveness depends on growth rate, itself a function of leaf mass fraction (LMF) and leaf nitrogen per unit mass (Nm). Architectural defence against vertebrates (which includes spinescence) limits herbivore access to plant leaf materials, and partly depends on leaf-size reduction, thereby compromising LMF. Low nutrient defence requires that leaf material is of insufficient nutrient value to support vertebrate metabolic requirements, which depends on low Nm. Thus there is an enforced tradeoff between LMF and Nm, leading to distinct trait suites for each defence strategy. We demonstrate this tradeoff by showing that numerous traits can be distinguished between 28 spinescent (architectural defenders) and non-spinescent (low nutrient defenders) of Fabaceae tree species from savannas, where mammalian herbivory is an important constraint on plant growth. Distributions of the strategies along an LMF-Nm tradeoff further provides a predictive and parsimonious explanation for the uneven distribution of spinescent and non-spinescent species across water and nutrient gradients.

Water storage in the stems of woody plants contributes to their responses to short-term water shortages. To estimate the contribution of water storage to the daily water budget of trees, time lags of sap flow between different positions of trunk are used as a proxy of stem water storage. In lianas, another large group of woody species, it has rarely been studied whether stored water functions in their daily water use, despite their increasing roles in the carbon and water dynamics of tropical forests caused by their increasing abundance. We hypothesized that lianas would exhibit large time lags due to their extremely long stems, wide vessels and large volume of parenchyma in the stem. We examined time lags in sap flow, diel changes of stem volumetric water content (VWC) and biophysical properties of sapwood of 19 lianas and 26 co-occurring trees from 27 species in 4 forests (karst, tropical seasonal, flood plain and savanna) during a wet season. The plants varied in height/length from5 to60 m. The results showed that lianas had significantly higher saturated water content (SWC) and much lower wood density than trees. Seven of 19 liana individuals had no time lags; in contrast, only 3 of 26 tree individuals had no time lags. In general, lianas had shorter time lags than trees in our data set, but this difference was not significant for our most conservative analyses. Across trees and lianas, time lag duration increased with diurnal maximum changeable VWC but was independent of the body size, path length, wood density and SWC. The results suggest that in most lianas, internal stem water storage contributes little to daily water budget, while trees may rely more on stored water in the stem.

Compositional shifts of bunchgrass species in the Southern Tall Grassveld in response to different combinations of non-selective mowing and burning appear to reflect differences in growth strategy among species, but there are few studies of South African grasses designed to test this. A descriptive study was undertaken both to observe how different species allocated resources in response to different defoliation treatments imposed at the start of spring, as it was thought that these responses might be critical for an understanding of tiller dynamics and compositional change in bunch grasslands. The study recorded the reproductive growth response of two spring-flowering species, Themeda triandra and Eragrostis curvula, subjected to three defoliation treatments: no defoliation (No Mow), defoliation during the previous summer (Summer Mow), and defoliation in early spring (Early Spring Mow). Plant growth response was separated into primary growth, measured as individual organ extension on individual phytomers, and secondary growth, measured as the number of secondary tillers recruited per live primary tiller. Phytomer growth depended on treatment and species. For either species, organ extension was greater for the No Mow treatment than for either of the two defoliated treatments. Tillers of E.curvula were substantially larger and grew faster than T.triandra tillers. In addition, apical meristems of E.curvula remained close to the ground until flowering. These combined differences are consistent with E.curvula being able to outcompete T.triandra in less-frequently defoliated swards. Secondary tiller recruitment was significantly related to defoliation treatment and species. Tiller recruitment was substantially lower on the No Mow treatment than for the two defoliation treatments, and tiller recruitment was greater for T. triandra plants than for E.curvula plants. Accumulated blade length was negatively related to tiller recruitment. Results suggest that tiller recruitment was limited by nutrient demand of primary structures, a consequence of which is that T.triandra will recruit more tillers than E.curvula when defoliation opens up space, accounting for T.triandra's dominance on more regularly-defoliated treatments.African Journal of Range & Forage Science 2005, 22(1): 29–36

Summary 1 Bunchgrasses are clonal plants whose dominance of moist grasslands worldwide is maintained largely through tiller recruitment. Tiller recruitment in clonal plants is a subset of the problem of lateral bud outgrowth in higher plants. This paper proposes that three currently competing hypotheses of lateral bud outgrowth – apical dominance; the nutrition hypothesis; and photosensitivity to the red : far-red light ratio – all operate in a manner dependent on environment and plant form. 2 The evidence for each hypothesis is reviewed, following which an integrated model is provided that links the three hypotheses into a cohesive strategy. Consequently we assess tiller recruitment by bunchgrasses in terms of the constraints of their functional growth form and their environment. Of the mineral nutrients, only nitrogen is considered because it is the only nutrient whose relationship with tiller recruitment is well established. 3 The integrated model maintains the accepted paradigm that actual bud release is hormonally controlled by the auxin : cytokinin ratio, although local nutrient concentrations may also be inhibitory. Importantly, each hormone is controlled by local signals in the shoots and roots, respectively, facilitating appropriate responses to environmental conditions. Auxin production and export from the shoots is moderated by phytochrome responses to red : far-red light ratios. Cytokinin production is mediated by root N concentration which, in turn, is a function of N absorption from the soil and seasonal reallocation of tissue N. 4 The growth form of bunchgrasses and the environment in which they are found emphasize that N has a strong mediatory role over tiller production which allows the grass plant to respond appropriately to shifts in this limiting resource. This suggests that control of lateral bud outgrowth may have an evolutionary basis in resource competition for N.

It is claimed that high returns can be achieved from hunting and ecotourism operations. As a result wildlife production is a rapidly growing form of land-use in South Africa. Lately, rural African communities have approached regional conservation agencies for aid to establish small game reserves so that they too may benefit from wildlife production. However, wildlife operations have high input costs relative to domestic stock operations and no attempt has been made to determine the effect of property size on the costs and revenue generated by wildlife. This paper attempts to develop a method for identifying the relevant economic variables of wildlife production, subsistence production and commercial beef production and the revenues that these separate land-uses generate. Thence to observe their relationship with property size by means of an illustrative example. In this way the size ranges for which each of the three land-uses is most appropriate can be determined. Finally, the method is evaluated against the results of the example to identify future refinement. The results of this example indicate that the profit curve of wildlife rises far more steeply than those of either subsistence production or commercial beef production. However, due to the effect of high input costs associated with wildlife, both commercial and subsistence beef production are more profitable at small land sizes. This indicates that investing large sums of money into small game reserves of the order of 3000 ha or less may not be justified on the basis of profits alone.

Background and Aims Plant relative growth rate (RGR) depends on biomass allocation to leaves (leaf mass fraction, LMF), efficient construction of leaf surface area (specific leaf area, SLA) and biomass growth per unit leaf area (net assimilation rate, NAR). Functional groups of species may differ in any of these traits, potentially resulting in (1) differences in mean RGR of groups, and (2) differences in the traits driving RGR variation within each group. We tested these predictions by comparing deciduous and evergreen savanna trees. Methods RGR, changes to biomass allocation and leaf morphology, and root non-structural carbohydrate reserves were evaluated for juveniles of 51 savanna species (34 deciduous, 17 evergreen) grown in a common garden experiment. It was anticipated that drivers ofRGRwould differ between leaf habit groups because deciduous species have to allocate carbohydrates to storage in roots to be able to flush leaves again, which directly compromises their LMF, whereas evergreen species are not subject to this constraint. Key Results Evergreen species had greaterLMFandRGRthan deciduous species. Amongdeciduous speciesLMF explained 27% of RGR variation (SLA 34% and NAR 29 %), whereas among evergreen species LMF explained between 2 and 17% of RGR variation (SLA 32–35% and NAR 38–62 %). RGR and LMF were (negatively) related to carbohydrate storage only among deciduous species. Conclusions Trade-offs between investment in carbohydrate reserves and growth occurred only among deciduous species, leading to differences in relative contribution made by the underlying components of RGR between the leaf habit groups. The results suggest that differences in drivers ofRGRoccur among savanna species because these have different selected strategies for coping with fire disturbance in savannas. It is expected that variation in the drivers of RGR will be found in other functional types that respond differently to particular disturbances.

Changes in land use may lead to increased soil nutrient levels in many ecosystems (e.g. due to intensification of agricultural fertilizer use). Plant species differ widely in their response to differences in soil nutrients, and for savannas it is uncertain how this nutrient enrichment will affect plant community dynamics. We set up a large controlled short-term experiment in a semi-arid savanna to test how water supply (even water supply vs. natural rainfall) and nutrient availability (no fertilisation vs. fertilisation) affects seedlings’ above-ground biomass production and leaf-nutrient concentrations (N, P and K) of broad-leafed and fine-leafed tree species. Contrary to expectations, neither changes in water supply nor changes in soil nutrient level affected biomass production of the studied species. By contrast, leaf-nutrient concentration did change significantly. Under regular water supply, soil nutrient addition increased the leaf phosphorus concentration of both fine-leafed and broad-leafed species. However, under uneven water supply, leaf nitrogen and phosphorus concentration declined with soil nutrient supply, this effect being more accentuated in broad-leafed species. Leaf potassium concentration of broad-leafed species was lower when growing under constant water supply, especially when no NPK fertilizer was applied. We found that changes in environmental factors can affect leaf quality, indicating a potential interactive effect between land-use changes and environmental changes on savanna vegetation: under more uneven rainfall patterns within the growing season, leaf quality of tree seedlings for a number of species can change as a response to changes in nutrient levels, even if overall plant biomass does not change. Such changes might affect herbivore pressure on trees and thus savanna plant community dynamics. Although longer term experiments would be essential to test such potential effects of eutrophication via changes in leaf nutrient concentration, our findings provide important insights that can help guide management plans that aim to preserve savanna biodiversity.

† Background and Aims Biomass partitioning for resource conservation might affect plant allometry, accounting for a substantial amount of unexplained variation in existing plant allometry models. One means of resource conservation is through direct allocation to storage in particular organs. In this study, storage allocation and biomass allometry of deciduous and evergreen tree species from seasonal environments were considered. It was expected that deciduous species would have greater allocation to storage in roots to support leaf regrowth in subsequent growing seasons, and consequently have lower scaling exponents for leaf to root and stem to root partitioning, than evergreen species. It was further expected that changes to root carbohydrate storage and biomass allometry under different soil nutrient supply conditions would be greater for deciduous species than for evergreen species. † Methods Root carbohydrate storage and organ biomass allometries were compared for juveniles of 20 savanna tree species of different leaf habit (nine evergreen, 11 deciduous) grown in two nutrient treatments for periods of 5 and 20 weeks (total dry mass of individual plants ranged from 0.003 to 258.724 g). † Key Results Deciduous species had greater root non-structural carbohydrate than evergreen species, and lower scaling exponents for leaf to root and stem to root partitioning than evergreen species. Across species, leaf to stem scaling was positively related, and stem to root scaling was negatively related to root carbohydrate concentration. Under lower nutrient supply, trees displayed increased partitioning to non-structural carbohydrate, and to roots and leaves over stems with increasing plant size, but this change did not differ between leaf habits. † Conclusions Substantial unexplained variation in biomass allometry of woody species may be related to selection for resource conservation against environmental stresses, such as resource seasonality. Further differences in plant allometry could arise due to selection for different types of biomass allocation in response to different environmental stressors (e.g. fire vs. herbivory).

Summary 1. Drought stress selects for a suite of plant traits at root, stem and leaf level. Two strategies are proposed for trees growing in seasonally water-stressed environments: drought tolerance and drought avoidance. These are respectively associated with evergreen phenology, where plants retain their leaves throughout the year, and deciduous phenology, where plants drop their leaves during dry seasons. Evergreen species are thought to have leaf traits supporting lower photosynthesis and transpiration rates, in order to conserve water during dry periods. 2. We evaluated 18 morphological, chemical and physiological leaf traits of 51 abundant savanna tree species that differed in leaf habit (deciduous and evergreen), selected from two climate types (semi-arid and humid) in three continents (Australia, Africa and South America) (annual rainfall range: 500–1550 mm), and grown in a common garden experiment. We hypothesised that evergreen species have more conservative water use and differ more across climate types than deciduous species because evergreen species are forced to endure extended water deficits during dry seasons. 3. Trait shifts between semi-arid and humid savannas did not differ between evergreen and deciduous species. 4. Evergreen species had similar assimilation rates but lower photosynthetic water-use efficiency (PWUE) than deciduous species, possibly to extend their leaf lifespans by protecting their photosynthetic machinery from overheating through evaporative cooling. 5. Species of humid and semi-arid environments did not differ with respect to assimilation rate or PWUE, but semi-arid species did have smaller leaf sizes and greater leaf potassium and phosphorus concentrations. These traits may enable semi-arid species to maximize growth during episodes of favourable moisture availability. 6. Species from the three continents differed in their leaf traits. These probably reflect the greater proportion of evergreen species in Australia as compared to the other continents and generally infertile soils in the South American sampling sites compared to the wider fertility range in the African sites. 7. Synthesis: Water stress in savannas does not select for more conservative water use, but may select for rapid adjustment to prevailing water conditions and for heat avoidance mechanisms.

Climate warming over the next century is expected to have a large impact on the interactions between pathogens and their animal and human hosts. Vector-borne diseases are particularly sensitive to warming because temperature changes can alter vector development rates, shift their geographical distribution and alter transmission dynamics. For this reason, African trypanosomiasis (sleeping sickness), a vector-borne disease of humans and animals, was recently identified as one of the 12 infectious diseases likely to spread owing to climate change. We combine a variety of direct effects of temperature on vector ecology, vector biology and vector–parasite interactions via a disease transmission model and extrapolate the potential compounding effects of projected warming on the epidemiology of African trypanosomiasis. The model predicts that epidemics can occur when mean temperatures are between 20.7°C and 26.1°C. Our model does not predict a large-range expansion, but rather a large shift of up to 60 per cent in the geographical extent of the range. The model also predicts that 46–77 million additional people may be at risk of exposure by 2090. Future research could expand our analysis to include other environmental factors that influence tsetse populations and disease transmission such as humidity, as well as changes to human, livestock and wildlife distributions. The modelling approach presented here provides a framework for using the climate-sensitive aspects of vector and pathogen biology to predict changes in disease prevalence and risk owing to climate change.

Savannas exhibit enormous spatiotemporal variability in woody and herbaceous biomass, structure, and plant functional forms; and the determinants of these are poorly understood (Bond, 2008; Lehmann et al., 2009). This is not surprising given that savannas are subject to an array of environmental drivers. Savannas occur over a huge range of climate conditions: mean annual precipitation (MAP) alone ranges from 150 mm to more than 2800 mm (Solbrig, 1996; Sankaran et al., 2005). Soil properties (fertility, texture, and depth) and irradiance also vary widely across savannas (Solbrig, 1996). Additionally, large areas of savanna are subject to defoliation by herbivores and fire, two quite different forms of defoliation on plants with consequent effects on their (re)growth, which also vary substantially over the biome (Olff et al., 2002; Bond and Keeley, 2005).

Interactions between structural architecture and resource allocation affect the ability of plants to utilise environmental resources. Architecture defines the structural layout and relationships of organs and other structural units at different hierarchical levels in plants. Resource allocation determines how competing structural units are awarded resources at different levels of hierarchy. Functional-structural plant models combine architecture and resource allocation as interacting components of plant growth and functioning. Existing functional-structural plant models concentrate on growth of unitary trees and therefore, lack sufficient structural definition to simulate growth of clonal plants. On the other hand, simulation models designed to consider clonal growth rarely attempt to simulate clonal architecture at a more detailed level than individual ramets. This paper introduces a functional-structural type model, TILLERTREE, which integrates the architectural growth of bunchgrasses with resource capture and allocation of nitrogen and carbohydrate. Resource allocation is implemented using a procedural algorithm based on object hierarchy and priority, and not mechanistically. The model is used to illustrate that growth of bunchgrass clones is regulated by patterns of resource allocation between competing units at low levels of hierarchy, by considering the effect of resource rules controlling secondary tiller recruitment on clonal growth. Simulations are conducted using a chosen model C4 bunchgrass species Themeda triandra.