Despite their key role in biodiversity conservation, forests in the Congo Basin are increasingly threatened by human activities, but it remains challenging to assess the impact of forest degradation under a more or less intact canopy. Likewise, forest recovery following agricultural abandonment remains poorly understood in the Congo Basin. Here, we surveyed 125 vegetation quadrats across 25 forest inventory plots in the Yangambi area. We aimed to find associations between both selective logging and forest recovery, and a range of forest community and tree community trait characteristics, as compared to reference undisturbed old-growth forest. We found that plots in undisturbed old-growth forest harboured both more tree individuals and tree species with a higher wood density as compared to plots in disturbed old-growth forest. In addition, their tree community composition was significantly different, whereas species diversity recovered since relatively recent agricultural abandonment (< 60 years), community composition and forest structure remained significantly different from the plots in undisturbed old-growth forest. Our study provides some insights into the rate of forest recovery in the Congo basin after agricultural abandonment and highlights the need of proper conservation of the remaining relatively undisturbed old-growth forests. Finally, we stress the need for more extensive vegetation surveys in the Congo Basin to further unravel the effects of anthropogenic disturbance.

In order to assess the response of cocoa trees to drought, changes in water status, gas exchange, leaf carbon isotopic ratio (δ13C), photochemical activity, and leaf N and chlorophyll content during the rainy and dry season were measured in 31 Venezuelan cocoa clones (17 Trinitarios, 6 Criollos, and 8 Modern Criollos) grown in a common garden. Drought caused a 40% decrease in water potential (ψ) in all but the Modern Criollos, and a reduction in net photosynthetic rate (A) and stomatal conductance (gs) without an increase in instantaneous water use efficiency (WUE) in 93% of clones, and an increase in δ13C (long-term WUE) in 74% of clones; these responses suggest differences in tolerance to drought among clones. A positive correlation between A and both gs and leaf N content was found for all genotypes. Leaf N content, chlorophyll content, and photochemical activity were reduced during drought, suggesting that metabolism was also inhibited. The best performance during drought was shown by Modern Criollos with the highest WUE, while five Trinitario clones seemed to be less sensitive to drought, since neither chlorophyll, N, total soluble protein concentration, nor gs changed with drought, indicating that those Trinitario clones, with lower A, have a conservative water use. Modern Criollos showed no reductions in either ψ or gs; A remained unchanged, as did WUE, which was the highest, suggesting that these clones would be more successful in environments with low water availability. Our results indicate large variation in physiological response to drought over a range of parameters, suggesting possible differences in tolerance among clones.

Understanding how plants alter their growth in response to interplant competition is an overlooked but complex problem. Previous studies have characterized the effect of light and water stress on soybean or common ragweed growth in monoculture, but no study has characterized soybean and common ragweed growth in mixture. A field study was conducted in 2015 and 2016 at the University of Nebraska-Lincoln to characterize the growth response of soybean and common ragweed with different irrigation levels and intraspecific and interspecific interference. The experiment was arranged in a split-plot design with irrigation level (0, 50%, 100% replacement of simulated evapotranspiration) as the main plot and common ragweed density (0, 2, 6, 12 plants m−1 row) as the subplot. Crop- and weed-free controls and three mixture treatments were included as subplots. Periodic destructive samples of leaf area and biomass of different organ groups were collected, and leaf area index (LAI), aboveground biomass partitioning, specific leaf area (SLA), and leaf area ratio (LAR) were calculated. Additionally, soybean and common ragweed yield were harvested, and 100-seed weight and seed production were determined. Soybean did not alter biomass partitioning, SLA, or LAR in mixture with common ragweed. Soybean LAI, biomass, and seed size were affected by increasing common ragweed density. Conversely, common ragweed partitioned less new biomass to leaves and increased SLA in response to increased interference. Common ragweed LAI, biomass, and seed number were reduced by the presence of soybean and increasing common ragweed density; however, seed weight was not affected. Results show that adjustment in biomass partitioning, SLA, and LAR is not the method that soybean uses to remain plastic under competition for light. Common ragweed demonstrated plasticity in both biomass partitioning and SLA, indicating an ability to maintain productivity under intra- and inter-specific competition for light or soil resources.

The effect of black and eastern black nightshade on the amount of photosynthetically active radiation (PAR) intercepted by a processing tomato canopy was studied along with the correlation between PAR and tomato growth and yield. During 1989 and 1990, black and eastern black nightshade were established at densities of 0 to 4.8 m−2 within rows of transplanted, irrigated processing tomatoes. Increasing the density of either nightshade species decreased the number of tomato fruit; however, eastern black nightshade reduced tomato yield more than black nightshade. Eastern black nightshade was taller than the tomatoes, reducing PAR reaching the top of the tomato canopy. PAR reaching the top of the tomato canopy was positively correlated with yield and negatively correlated with eastern black nightshade density. Eastern black nightshade intraspecific competition decreased both stem and berry weight. Black nightshade was never taller than tomatoes and did not affect PAR reaching the top of the crop canopy. Increasing the density of black nightshade decreased berry dry weight but increased the weight of stems and leaves.

Redroot pigweed is a troublesome weed in the sorghum-growing regions of North America. In 1994 and 1995, field studies were conducted at two locations near Manhattan, KS, to determine the influence of redroot pigweed density and environmental conditions on physiological determinants of redroot pigweed growth: duration of plant growth, light interception, radiation-use efficiency, and dry matter partitioning. In addition, specific leaf area was determined. Redroot pigweed was seeded at monoculture densities of 2, 4, and 12 plants m−1 of row each year at each location. Duration of redroot pigweed growth was not influenced by plant density. Light interception was defined as a simple exponential function of leaf area index. Specific leaf area did not change over the season and averaged 135 cm2 g−1. Partitioning of redroot pigweed dry matter was not influenced by plant density or environmental conditions but did not change within vegetative and reproductive stages. Radiation-use efficiency was not influenced by redroot pigweed density; the most reliable estimate was 1.74 g dry matter MJ−1 of intercepted photosynthetically active radiation. Physiological determinants described were not affected by redroot pigweed density or environmental conditions and therefore provide a starting point for the development of a redroot pigweed growth module. The module could be coupled with available crop growth models (e.g., the sorghum growth model SORKAM) to simulate redroot pigweed–sorghum competition.

The objectives were to compare the growth of black and eastern black nightshade and develop predictive models for their growth. Black and eastern black nightshade were planted on June 3 and 23, and July 12 in 1988 and May 28, June 17, and July 10 in 1989. Exponential models were strongly correlated with the growth of both species across all planting dates. Eastern black nightshade produced more biomass than black nightshade, although weight of berries was equivalent. Leaf area per plant 60 d after planting was five times greater for eastern black nightshade than black nightshade. Eastern black nightshade responded to self-shading by increasing specific leaf area.

Field studies were conducted in Colorado and New Mexico to examine growth and development of spurred anoda accessions from Colorado, Mississippi, New Mexico, and North Carolina. Accessions were grown in a common garden in both locations. Leaf and stem weight ratios, leaf area ratio, and leaf area per plant were determined. North Carolina and Mississippi accessions were similar in morphology and appearance. Leaf shape, degree of pubescence, and coloration were different in the Colorado and New Mexico accessions. At both sites, the Colorado accession was taller and the canopy wider than other accessions. In Colorado in 1993, North Carolina and New Mexico accessions had the highest total weight followed by Colorado, then Mississippi. In 1994, final total weights of North Carolina, Mississippi, and New Mexico accessions were similar and greater than the Colorado accession. All accessions had similar final total weights in New Mexico in 1993. In 1994, Mississippi, North Carolina, and New Mexico accessions had similar total weights. The Colorado accession flowered earlier than other accessions. Seeds from Mississippi and North Carolina accessions grown in Colorado were heavier than the New Mexico or Colorado accession. This research demonstrates why making inferences of weed biology for variable species that occur over diverse geographic and climatic conditions is difficult and why regionally specific data are needed for variable species.

Field experiments were conducted to study the competition effect of winter wheat planted in a square arrangement and Italian ryegrass planted randomly on biomass yields of both species, ryegrass seed yield, N use efficiency, and progeny seed germination. Increases in wheat density up to 800 plants/m2 reduced ryegrass seed yield by 87% but increased its harvest index up to 42% compared to its monoculture yield. Species densities and their interactions accounted for 66 to 73% of the total variation in per-unit area biomass of species, and their association was more favorable to ryegrass biomass than wheat. Seeds of each species had three times greater nitrogen percentage than did shoots. Intra- and interspecific competition increased nitrogen percentage in wheat seeds. In Italian ryegrass, only interspecific competition increased N percentage in seeds. Although total nitrogen uptake by winter wheat was three times greater than in Italian ryegrass, Italian ryegrass was two times more efficient than wheat at producing biomass per unit of N taken up and specific leaf area at heading stage in mixture. Germination percentages of progeny seeds of both species in mixtures were greater in presence of high densities of the companion species than in their monocultures. Nitrogen was not the main limiting factor for competition between winter wheat and Italian ryegrass in this study.

Characterizing the response of weeds to canopy shade is important for improved understanding of crop–weed competition and weed population dynamics. In 2000 and 2001, field studies were conducted in central New York state to examine the influence of three neighbor types (none, broccoli, or broccoli plus winter rye) and two locations (between or within rows of broccoli) on the morphology, phenology, and seed germination characteristics of Powell amaranth. Reductions in light availability and in the ratio of red-to-far red light were associated with increases in (1) partitioning of dry weight to stem tissue, (2) stem elongation, and (3) specific leaf area. Canopy shade also resulted in fewer main leaves at flowering and a reduced rate of leaf appearance but had no effect on the number of days to flowering. The relationship between Powell amaranth fecundity and aboveground dry weight was allometric, with both parameters declining significantly under competition. The weight of seeds produced did not vary significantly according to the competitive environment experienced by the maternal parent. However, the germination percentage of viable seeds was 40 to 50% lower for seeds maturing on plants grown under competition than without competition. Reductions in the number of main leaves at flowering and increased seed dormancy may be adaptive responses to canopy shade. Both mechanistic crop–weed competition models and population dynamic models would benefit from incorporation of data on the phenotypic plasticity of morphology, phenology, and seed germination characteristics of weeds.

A 2-yr field study was conducted to compare growth characteristics of 24 Palmer amaranth accessions collected from across the indigenous range of the species in the United States. Variation in growth and development of Palmer amaranth was noted among accessions based on leaf area ratio (LAR), specific leaf area (SLA), net assimilation rate (NAR), and stem leaf ratio (SLR), but only SLR varied across harvest intervals among accessions. Accessions collected across the range of Palmer amaranth in the United States displayed variation in growth and development based on differences in LAR, SLA, NAR, and SLR. Observed differences among accessions indicate the existence of Palmer amaranth ecotypes.

Whole plant form and function vary spectacularly across the seed plants. In recent years, plant evolutionary ecologists have begun to document this diversity on large geographic scales by analysing ‘functional traits’ that are indicative of whole plant performance across environmental gradients (Swenson & Enquist 2007, Wright et al. 2004). Despite the high degree of functional diversity in tropical forests, convergence in function does occur locally along successional or light gradients (Bazzaz & Pickett 1980, Swaine & Whitmore 1988).

Although the potential contribution to tropical tree species coexistence of niche differentiation along light gradients has received much attention, the degree to which species perform differentially along soil resource gradients remains unclear. To examine differential growth response to soil resources, we grew seedlings of nine tropical tree species at 6.0% of full sun for 12 mo in a factorial design of two soil types (clay and white sand), two phosphate fertilization treatments (control and addition of 100 mg P kg−1) and two watering treatments (field capacity and water limitation to one-third field capacity). Species differed markedly in biomass growth rate, but this hierarchy was almost completely conserved across all eight treatments. All species grew more slowly in sand than clay soils, and no species grew faster with phosphate additions. Only Eperua grandiflora and E. falcata showed significant growth increases in the absence of water limitation. Faster-growing species were characterized by high specific leaf area, high leaf allocation and high net assimilation rate but not lower root allocation. Slower-growing species exhibited greater plasticity in net assimilation rate, suggesting that tolerance of edaphic stress in these species is related more to stomatal control than to whole-plant carbon allocation. Although relative growth rate for biomass was correlated with both its physiological and morphological components, interspecific differences were best explained by differences in net assimilation rate across six of the eight treatments. A suite of traits including high assimilation and high specific leaf area maintains rapid growth rate of faster-growing species across a wide gradient of soil resources, but the lack of plasticity they exhibit may compromise their survival in the poorest soil environments.

Tropical pioneer tree species are considered as a functional group characterized by a suite of ecological characteristics such as high light demand and high photosynthetic capacities. This study compared the photosynthetic characteristics of eight co-existing pioneer tree species in 3–4-y-old and about 6-m-tall secondary forest stands in Sulawesi, Indonesia. Its objectives were (1) to determine the range and interspecific variation in six photosynthetic parameters, and (2) to identify morphological and chemical leaf traits that can predict light-saturated net photosynthetic rates (on a leaf area or leaf mass basis, Amax-area or Amax-mass). Species averages of Amax-area in sun leaves ranged between 14.2 and 20.3 μmol m−2 s−1 (mean 17.5) which is high compared with literature data. Among the co-existing species, average leaf size (56–896 cm2) differed by a factor of 16, specific leaf area (SLA, 10.7–21.4 m2 kg−1) and leaf nitrogen content (19.6–33.9 g kg−1) twofold. At the species level, Amax-area was not correlated with leaf N content but decreased significantly with leaf size. Amax-mass showed a higher interspecific variation than Amax-area, and was positively correlated with SLA and leaf N content (slope: 13.4 nmol CO2 g N−1 s−1). Both, Amax-area and Amax-mass were more closely related to leaf morphological attributes than to leaf N. We conclude that the tropical pioneer tree species studied do not form a homogeneous functional group in terms of photosynthetic performance. Rather, a considerable variation in leaf morphology and nitrogen content exists, which also shows up in a substantial variation in Amax-mass and, to a lesser extent, in Amax-area.

To clarify the role of seasonal change, competitive response and nutrient availability in the competitive asymmetry of grassland species a competition experiment was conducted on Holcus lanatus, Anthoxanthum odoratum and Festuca ovina, which represent a successional sequence of decreasing nutrient availability. Seven harvests were taken over two growing seasons. At each harvest the dry weight of plant parts, dead leaves, leaf area and plant height were measured. Three key traits that determine the successional status of the species were studied: specific leaf area, specific shoot height, and dead leaf fraction.

The response of these traits to competition appeared to be limited and insufficient to change the competitive relations in the experiment. However, all three traits showed marked seasonal changes which resulted in superior growth and survival in winter of the species adapted to nutrient-poor environments. The findings support the theory that competitive asymmetry increases at higher nutrient levels. It is postulated that the directionality of light makes it possible for the dominant species to monopolize this resource more easily than nutrients.

Laboratory experiments have shown a large difference in specific leaf area (SLA, leaf area: leaf mass) between species from nutrient-poor and nutrient-rich habitats, but no systematic difference in the construction costs (the amount of glucose required to construct 1 g biomass). We examined how far these patterns are congruent with those from field-grown plants. An analysis was made of the vegetation in a range of grasslands and heathlands differing in productivity. The SLA of the dominant species in 15 different habitats was determined, as well as chemical composition and construction costs of bulk samples of leaves. SLA in the field was generally lower than in the laboratory, but showed consistency in that the ranking across species remained the same. Species from highly productive habitats had higher SLA than those from sites of low productivity, although individual species sometimes deviated substantially from the general trend. Construction costs were similar for plants from different habitats. This was mainly due to the positive correlation between an expensive class of compounds (proteins) and a cheap one (minerals).

This study examines interrelationships between eight leaf attributes (specific leaf mass, area, dry mass, lamina thickness, mesophyll cell number per cm2, mesophyll cell volume, chloroplast volume, and number of chloroplasts per mesophyll cell) in field-grown plants of 94 species from the Eastern Pamir Mountains, at elevations between 3800 and 4750 m. Unlike most other mountain areas, the Eastern Pamirs, Karakorum system, Tadjikistan provide localities where low temperatures and radiation combine with moisture stress at high altitudes. For all the attributes measured, significant differences were found between plants with different mesophyll types. Leaves with dorsiventral palisade structure (dorsal palisade, ventral spongy mesophyll cells) had thicker leaves with larger but fewer mesophyll cells, containing more and larger chloroplasts. These differences in mesophyll type are reflected in differences in the total surface of mesophyll cells per unit leaf area (Ames/A) or volume (Ames/V). Plants with isopalisade leaf structure (palisade cells under both dorsal and ventral surfaces) are more commonly xerophytes and their increased values of Ames/A and Ames/V decrease CO2 mesophyll resistance, which is an important adaptation to drought. Path analysis shows the critical importance of mesophyll cell volume in leading to the covariance between the different leaf attributes and hence to specific leaf mass (SLM), even though mesophyll cell volume is not itself strongly correlated with SLM. This is because mesophyll cell volume increases SLM through its effects on leaf thickness and chloroplast number per cell, but decreases SLM through its negative effect on mesophyll cell density.

Models have been formulated for monospecific stands in which canopy photosynthesis is determined by the vertical distribution of leaf area, nitrogen and light. In such stands, resident plants can maximize canopy photosynthesis by distributing their nitrogen parallel to the light gradient, with high contents per unit leaf area at the top of the vegetation and low contents at the bottom. Using principles from game theory, we expanded these models by introducing a second species into the vegetation, with the same vertical distribution of biomass and nitrogen as the resident plants but with the ability to adjust its specific leaf area (SLA, leaf area[ratio ]leaf mass). The rule of the game is that invaders replace the resident plants if they have a higher plant carbon gain than those of the resident plants. We showed that such invaders induce major changes in the vegetation. By increasing their SLA, invading plants could increase their light interception as well as their photosynthetic nitrogen-use efficiency (PNUE, the rate of photosynthesis per unit organic nitrogen). By comparison with stands in which canopy photosynthesis is maximized, those invaded by species of high SLA have the following characteristics: (1) the leaf area index is higher; (2) the vertical distribution of nitrogen is skewed less; (3) as a result of the supra-optimal leaf area index and the more uniform distribution of nitrogen, total canopy photosynthesis is lower. Thus, in dense canopies we face a classical tragedy of the commons: plants that have a strategy to maximize canopy carbon gain cannot compete with those that maximize their own carbon gain. However, because of this strategy, individual as well as total canopy carbon gain are eventually lower. We showed that it is an evolutionarily stable strategy to increase SLA up to the point where the PNUE of each leaf is maximized.

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.

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.