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Light Competition (light + competition)
Selected AbstractsTrade-offs between the shade-avoidance response and plant resistance to herbivores?FUNCTIONAL ECOLOGY, Issue 6 2005Tests with mutant Cucumis sativus Summary 1Plants exhibit adaptations to many stresses, including light competition and herbivory. The expression of these traits may interact negatively, potentially instigating a trade-off. 2We employed a combination of genetically altered Cucumis sativus varieties and phenotypic manipulations to test for trade-offs in field experiments. The different genetic lines of C. sativus were altered in their phytochrome-mediated shade responses and the production of terpenoid defence compounds. 3Cucumber plants constitutively expressing the shade-avoidance response had 93% more herbivory by specialist beetles compared with wild types. The long-hypocotyl mutants also produced leaves with fewer trichomes, greater toughness and a higher carbon to nitrogen ratio (C : N) than wild types. Plants lacking defensive cucurbitacins had 23% longer internodes than the cucurbitacin-producing line. 4We then manipulated the plant phenotype by artificially imposing neighbours' shade on plants with and without cucurbitacins. As expected, plants responded to shade by growing longer hypocotyls and first internodes, but few trade-offs were found between plant line and shade treatment and, although herbivory levels were very low, there was a trend towards reduced damage on shaded plants. 5The use of genetically altered plant lines provided strong evidence for the trade-off hypothesis, while phenotypic manipulations did not support the hypothesis. [source] Anthropogenic disturbance and the formation of oak savanna in central Kentucky, USAJOURNAL OF BIOGEOGRAPHY, Issue 5 2008Ryan W. McEwan Abstract Aim, To deepen understanding of the factors that influenced the formation of oak savanna in central Kentucky, USA. Particular attention was focused on the link between historical disturbance and the formation of savanna ecosystem structure. Location, Central Kentucky, USA. Methods, We used dendrochronological analysis of tree-ring samples to understand the historical growth environment of remnant savanna stems. We used release detection and branch-establishment dates to evaluate changes in tree growth and the establishment of savanna physiognomy. We contrasted our growth chronology with reference chronologies for regional tree growth, climate and human population dynamics. Results, Trees growing in Kentucky Inner Bluegrass Region (IBR) savanna remnants exhibited a period of suppression, extending from the establishment date of the tree to release events that occurred c. 1800. This release resulted in a tripling of the annual radial growth rate from levels typical of oaks suppressed under a forest canopy (< 1 mm year,1) to levels typical of open-grown stems (3 mm year,1). The growth releases in savanna trees coincided with low branch establishment. Over the release period, climatic conditions remained relatively constant and growth in regional forest trees was even; however, the growth increase in savanna stems was strongly correlated with a marked increase in Euro-American population density in the region. Main conclusions, Our data suggest that trees growing in savanna remnants originated in the understorey of a closed canopy forest. We hypothesize that Euro-American land clearing to create pasturelands released these trees from light competition and resulted in the savanna physiognomy that is apparent in remnant stands in the IBR. Although our data suggest that savanna trees originated in a forest understorey, this system structure itself may have been a result of an unprecedented lack of Native American activity in the region due to population loss associated with pandemics brought to North America by Euro-Americans. We present a hypothetical model that links human population dynamics, land-use activities and ecosystem structure. Our model focuses on the following three land-use eras: Native American habitation/utilization; land abandonment; and Euro-American land clearance. Ecological understanding of historical dynamics in other ecosystems of eastern North America may be enhanced through recognition of these eras. [source] Effects of size, competition and altitude on tree growthJOURNAL OF ECOLOGY, Issue 5 2007DAVID A. COOMES Summary 1,Understanding the factors influencing tree growth is central to forest ecology because of the significance of growth to forest structure and biomass. One of the simplest, yet most controversial growth models, proposed by Enquist and colleagues, predicts that stem-diameter growth scales as the one-third power of stem diameter. Recent analyses of large-scale data sets have challenged the generality of this theory and highlighted the influence of resource competition on the scaling of growth with size. 2Here we explore the factors regulating the diameter growth of 3334 trees of mountain beech (Nothofagus solandri var. cliffortioides) growing in natural single-species forests in New Zealand. Maximum-likelihood modelling was used to quantify the influences of tree size, altitude, the basal area of taller neighbours (BL) and the basal area of all neighbours (BT) on growth. Our interpretation of the models assumed that taller neighbours compete for light whereas all neighbours compete for nutrients. 3The regression analyses indicate that competition for light has a strong influence on the growth of small trees, whereas competition for nutrients affects trees of all sizes. These findings are consistent with experimental manipulation studies showing that competition for light and nutrients inhibits the growth of small mountain beech trees, and fertilizer application studies showing that nitrogen limits the growth of large trees. 4Tree growth declined with altitude. The regression analyses suggest that the intensity of light competition also declines with altitude, when trees with similar BT and BL values were compared along the gradient. These results are consistent with observations that trees become stunted and have more open canopies at high altitudes. 5Our study is the first to build the effects of competition and environment into Enquist's model of tree growth. We show that competitive interactions alter the scaling of mean growth rate with size, whereas altitude does not influence the scaling of potential growth rate with size. [source] Reconciling plant strategy theories of Grime and TilmanJOURNAL OF ECOLOGY, Issue 6 2005JOSEPH M. CRAINE Summary 1The theories of Grime and Tilman are ambitious attempts to unify disparate theories regarding the construction of plants, their interaction with the environment and the assembly of communities. After over two decades of parallel research, their ideas have not been reconciled, hindering progress in understanding the functioning of ecosystems. 2Grime's theories do not adequately incorporate the importance of non-heterogeneous supplies of nutrients and how these supplies are partitioned over long time scales, are inconsistent regarding the importance of disturbance in nutrient-limited habitats and need to reconsider the carbon economy of shade-tolerant plants. 3Failure to account for differences between aquatic and terrestrial systems in how resource supplies are partitioned led Tilman to develop a shifting set of theories that have become reduced in mechanistic detail over time. The most recent highlighted the reduction of nutrient concentrations in soil solution, although it can no longer be derived from any viable mechanistic model. The slow diffusion of nutrients in soils means that the reduction of average soil solution nutrient concentrations cannot explain competitive exclusion. 4Although neither theory, nor a union of the two, adequately characterizes the dynamics of terrestrial plant assemblages, the complementarity in their assumptions serve as an important foundation for future theory and research. 5Reconciling the approaches of Grime and Tilman leads to six scenarios for competition for nutrients and light, with the outcome of each depending on the ability of plants to pre-empt supplies. Under uniform supplies, pulses or patches, light competition requires leaf area dominance, while nutrient competition requires root length dominance. There are still important basic questions regarding the nature of nutrient supplies that will need to be answered, but recent research brings us closer to a unified set of theories on resource competition. [source] A test of the indirect facilitation model in a temperate hardwood forest of the northern French AlpsJOURNAL OF ECOLOGY, Issue 6 2003Jean-Philippe Pages Summary 1We tested the hypothesis that the more frequent occurrence of tree seedlings below the adult trees than in canopy openings might be explained by indirect facilitation. In a temperate hardwood forest, we compared the performance of five target tree seedlings (Picea abies, Abies alba, Fagus sylvatica, Acer pseudoplatanus and Quercus petraea), transplanted with or without a herbaceous competitor (Molinia caerulea), either within the forest or into experimentally created gaps. 2We quantified changes in understorey biomass, light penetration and available forms of soil nitrogen during three growing seasons. 3Photosynthetic photon flux density and total biomass of Molinia were significantly higher in the gap treatment than within the forest. Total available nitrogen was higher in the gaps in the absence of Molinia, but higher in the forest in the presence of Molinia. 4Quercus survival was very low within the forest because of fungal infection, whereas survival was very high for the four other tree species in all combinations of the two treatments. 5Although the competitive effect of Molinia on the growth of the tree seedlings was much greater in the gap treatment, seedling growth was lower within the forest. We conclude that the tree canopy imposed strong light competition, and that this direct negative influence was much greater than any indirect positive effect of increased availability of nutrients to tree seedlings, due to reduced nutrient uptake by Molinia. 6Target species responses to treatments were similar, despite strong differences in nitrogen requirements between species. This may be due to the overwhelming negative influence of the tree canopy in our experiment. [source] Ecological play in the coevolutionary theatre: genetic and environmental determinants of attack by a specialist weevil on milkweedJOURNAL OF ECOLOGY, Issue 6 2003Anurag A. Agrawal Summary 1We studied the genetic and environmental determinants of attack by the specialist stem-attacking weevil, Rhyssomatus lineaticollis on Asclepias syriaca. 2In natural populations, the extent of stem damage and oviposition were positively correlated with stem width, but not stem height. We hypothesized that both genotypic and environmental factors influencing stem morphology would affect attack by weevils. 3In a common garden study with 21 full-sib families of milkweed, both phenotypic and genetic correlations indicated that weevils impose more damage and lay more eggs on thicker stemmed plants. 4Of three other putative resistance traits, only latex production showed a negative genetic correlation with weevil attack. 5When neighbouring grasses were clipped to reduce light competition, focal milkweed plants received up to 2.6 times the photosynthetically active radiation and 1.6 times the red to far red ratio of light compared with plants with intact grass neighbours. Focal milkweed plants were therefore released from the classic neighbour avoidance response and had 20% shorter internode lengths, were 30% shorter, and had 90% thicker stems compared with controls. 6Clipping of grass neighbours resulted in nearly 2.7 times the damage and oviposition by stem weevils, thus supporting the hypothesis of an environmental or trait-mediated indirect influence on resistance. 7Although attack of plants by weevils strongly increases the probability of stem mortality, thicker stems experience lower mortality, thus counteracting the selective impact of weevil-induced plant mortality. 8The determinants of attack on milkweeds include both genetic variation for stem thickness and an indirect environmental influence of plant neighbours. If milkweeds and weevils are coevolving, the interaction is diffuse because the ecological neighbourhood is likely to modify the patterns of reciprocal natural selection. [source] Effects of resource competition and herbivory on plant performance along a natural productivity gradientJOURNAL OF ECOLOGY, Issue 2 2000René Van Der Wal Summary 1,The effects of resource competition and herbivory on a target species, Triglochin maritima, were studied along a productivity gradient of vegetation biomass in a temperate salt marsh. 2,Transplants were used to measure the impact of grazing, competition and soil fertility over two growing seasons. Three parts of the marsh were selected to represent different successional stages; Triglochin reached local dominance at intermediate biomass of salt-marsh vegetation. At each stage, three competition treatments (full plant competition, root competition only, and no competition) and three grazing treatments (full grazing, no grazing on Triglochin, and no grazing on Triglochin or neighbours) were applied to both seedlings and mature plants. 3,Competition and herbivory reduced biomass and flowering of Triglochin. The impact of grazing was strongest at the stage with the lowest biomass, while both herbivory and competition had a significant impact at the stage with the highest biomass. When plants were protected from direct herbivory, competition operated at all three successional stages. 4,Grazing reduced light competition when vegetation biomass was low or intermediate, but at high biomass there was competition for light even when grazing occurred. Herbivore exclusion increased the effects of plant competition. Except at low biomass, the negative impact of plant competition on Triglochin performance was greater than the positive effect of not being grazed. 5,Grazing played a minor role in seedling survival and establishment which were largely controlled by competitive and facilitative effects. 6,Once established, the persistence of Triglochin will be determined largely by grazing. Intense grazing in the younger marsh and increasing competition for light in the older marsh will restrict the distribution to sites with intermediate biomass. [source] How can we predict the effects of elevated CO2 on the balance between perennial C3 grass species competing for light?NEW PHYTOLOGIST, Issue 1 2002F. Teyssonneyre Summary ,,Changes in the balance between mixed plant species have been reported under elevated [CO2] compared with ambient atmospheric [CO2]. We hypothesized that species response to elevated CO2 in mixture can be explained by taking into account resource partitioning between mixed species. ,,This hypothesis was tested experimentally on three perennial C3 grass species (Lolium perenne, Festuca arundinacea and Holcus lanatus) grown in monocultures and in binary mixtures (Lolium,Festuca and Lolium,Holcus) under mild (frequent cuts) or severe (infrequent cuts) competition for light and at a high N supply (40 g N m,2). ,,Under mild competition for light, the dry matter yield response to elevated CO2 of the mixed grass species was similar to that observed in monocultures. By contrast, under severe light competition, the grass species that absorbed more light per unit leaf area (Holcus and Festuca), also had a greater response to elevated CO2 in mixture compared with monoculture. ,,Under our experimental conditions, we have shown that the dry matter yield response to CO2 in mixture can be predicted from both the species response in monoculture, and the light capture per unit leaf area in ambient CO2 of the mixed compared with the pure grasses. [source] | ||||||||||