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Competitive Effects (competitive + effects)
Selected AbstractsDifferential Employment Patterns for Citizens and Non-Citizens in Science and Engineering in the United States: Minting and Competitive EffectsGROWTH AND CHANGE, Issue 4 2004Sharon G. Levin ABSTRACT The consequences of the heavy inflow of foreign talent for U.S. scientists and engineers over the period 1973-1997 are examined using data from the Survey of Doctorate Recipients. Of particular interest is whether non-citizens trained in the United States have displaced citizens from jobs in science and engineering (S&E). Using a novel adaptation of the shift-share technique, it is shown that citizen S&E doctorates have fewer jobs in S&E and fewer academic jobs than their non-citizen counterparts for two reasons: the citizen doctoral population has experienced slower growth than the non-citizen doctoral population, and citizen S&E doctorates have been displaced. Whether the displacement observed was a voluntary response of citizens to the lure of better opportunities elsewhere or an involuntary response indicative of having been pushed out by foreign talent remains to be determined. [source] The Evolving Food Chain: Competitive Effects of Wal-Mart's Entry into the Supermarket IndustryJOURNAL OF ECONOMICS & MANAGEMENT STRATEGY, Issue 4 2009Emek Basker We analyze the effect of Wal-Mart's entry into the grocery market using a unique store-level price panel data set. We use ordinary least squares and two instrumental-variables specifications to estimate the effect of Wal-Mart's entry on competitors' prices of 24 grocery items across several categories. Wal-Mart's price advantage over competitors for these products averages approximately 10%. On average, competitors' response to entry by a Wal-Mart Supercenter is a price reduction of 1,1.2%, mostly due to smaller-scale competitors; the response of the "Big Three" supermarket chains (Albertson's, Safeway, and Kroger) is less than half that size. Low-end grocery stores, which compete more directly with Wal-Mart, cut their prices more than twice as much as higher-end stores. We confirm our results using a falsification exercise, in which we test for Wal-Mart's effect on prices of services that it does not provide, such as movie tickets and dry-cleaning services. [source] Competitive effects of grasses and woody plants in mixed-grass prairieJOURNAL OF ECOLOGY, Issue 4 2001Duane A. Peltzer Summary 1,Variation in the competitive ability of plant species may determine their persistence and abundance in communities. We quantified the competitive effects of grasses and woody plants in native mixed-grass prairie on the performance of transplant species and on resources. 2,We separated the effects of grasses, shrubs and intact vegetation containing both grasses and shrubs by manipulating the natural vegetation using selective herbicides to create four neighbourhood treatments: no neighbours (NN), no shrubs (NS), no grasses (NG) and all neighbours (AN). Treatments were applied to 2 × 2 m experimental plots located in either grass- or shrub-dominated habitats. The effects of grasses and shrubs on resource availability (light, soil moisture, soil available nitrogen) and on the growth of transplants of Bouteloua gracilis, a perennial tussock grass, and Elaeagnus commutata, a common shrub, were measured over two growing seasons. 3,Resource availability was two- to fivefold higher in no neighbour (NN) plots than in vegetated plots (NS, NG, AN) with grasses and shrubs having similar effects. Light penetration declined linearly with increasing grass or shrub biomass, to a minimum of about 30% incident light at 500 g m,2 shoot mass. Soil resources did not decline with increasing neighbour shoot or root mass for either grasses or shrubs, suggesting that the presence of neighbours was more important than their abundance. 4,Transplant growth was significantly suppressed by the presence of neighbours, but not by increasing neighbour shoot or root biomass, except for a linear decline in Bouteloua growth with increasing neighbour shoot mass in plots containing only shrubs. Competition intensity, calculated as the reduction in transplant growth by neighbours, was similar in both grass- and shrub-dominated habitats for transplants of Bouteloua, but was less intense in shrub-dominated habitats for the shrub Elaeagnus. Variation in the persistence and abundance of plants in communities may therefore be more strongly controlled by variation in the competitive effects exerted by neighbours than by differences in competitive response ability. [source] Adding magnesium to the silver-gill binding model for rainbow trout (Oncorhynchus mykiss)ENVIRONMENTAL TOXICOLOGY & CHEMISTRY, Issue 3 2001Melissa L. Schwartz Abstract Rainbow trout (Oncorhynchus mykiss; 2,17 g) were exposed to approximately 0.1 ,M silver as AgNO3 for 3 to 4 h in synthetic, ion-poor water (20 ,M Ca, 100 ,M Na, 150 ,M Cl, pH 7) to which was added Mg, Ca, or thiosulfate (S2O3). Gills were extracted and assayed for Ag using graphite furnace atomic absorption spectrophotometry. Up to 210 mM Mg (four fold the concentration of Mg in seawater) did not reduce accumulation of Ag by trout gills. The conditional equilibrium stability constant (K) for Mg at silver-binding sites on the gills was calculated to be log KMg-gillAg = 3.0, or approximately half-as-strong binding as for Ca at these sites. The inclusion of the Mg-gill stability constant into the original Ag-gill binding model increases the flexibility of the model, although the competitive effects of Mg are only important in sodium-poor systems. [source] Does an Industry Effect Exist for Initial Public Offerings?FINANCIAL REVIEW, Issue 4 2003Aigbe Akhigbe G14 Abstract We examine the impact of initial public offerings (IPOs) on rival firms and find that the valuation effects are insignificant. This insignificant reaction can be explained by offsetting information and competitive effects. Significant positive information effects are associated with IPOs in regulated industries and the first IPO in an industry following a period of dormancy. Significant negative competitive effects are associated with larger IPOs in competitive industries, those in relatively risky industries, those in high-performing industries, and those in the technology sector. IPO firms that use the proceeds for debt repayment appear to represent a more significant competitive threat to rival firms relative to IPO firms that use their proceeds for other purposes. [source] Intraspecific seed trait variations and competition: passive or adaptive response?FUNCTIONAL ECOLOGY, Issue 3 2009Cyrille Violle Summary 1The phenotype of offspring depends on the abiotic and biotic environment in which the parents developed. However, the direct effects of competition experienced by parent plants on single-seed traits are poorly documented despite their impact on plant fitness. 2We hypothesize that single-seed traits can differentially respond to the resource deficiencies of parent plants due to competition: seed quality may decrease as seed number does, magnifying the negative effects of competition for offspring (,passive response' hypothesis), or increase and then enhance offspring fitness to offset the reduction in offspring number (,adaptive response' hypothesis). Here we tested these hypotheses for four single-seed traits. We assessed the sensibility of their responses to changes in competition intensity due to species with different competitive effects and to contrasting soil nitrogen conditions. 3In a common-garden experiment, four single-seed traits related to fitness , seed mass, seed nitrogen concentration (SNC), germinability and the timing of germination , were measured on a phytometer species transplanted in 14 different neighbours grown in monoculture with and without soil nitrogen limitation. 4Under nitrogen-limiting conditions, the responses of SNC and of the timing of germination were passive and mainly related to the effects of neighbours on soil nitrogen availability, as shown by the increase in SNC with N-fixing neighbours. Within-individual seed mass variability decreased with increasing competition intensity, as an adaptive response to counterbalance the reduction in seed production. With nitrogen supplementation, competitors had no detectable effect on single-seed traits despite an overall increase in SNC and germination rate, confirming their nitrogen-dependent passive responses to competition. Germinability did not change among treatments. 5The impact of competition on single-seed traits depends on both phytometer trait identity and resource modulation by neighbours. The passive response of seed chemical composition to competitors may magnify the competitive effects on offspring. By contrast, the adaptive response of seed size variability may offset these competitive effects. As a consequence, experiments looking at the fitness consequences of competition should not only consider the effects on fitness parameters of a target plant but also on the offspring. [source] Relationships between the yield of perennial ryegrass and of small-leaved white clover under cutting or continuous grazing by sheepGRASS & FORAGE SCIENCE, Issue 3 2001T. A. Williams Seven varieties or advanced breeding lines of white clover (Trifolium repens L.), all of small leaf size, were grown separately in mixtures with perennial ryegrass (Lolium perenne L.) in an experiment encompassing three harvest years. Harvestable dry-matter (DM) yield measurements were taken of these mixtures and of perennial ryegrass monocultures under two management regimes: cutting and continuous sheep grazing. Considerable differences were observed in the harvestable DM yields of white clover, perennial ryegrass and total yields of the mixtures between plots containing different white clover varieties. White clover yields were generally higher under cutting, and perennial ryegrass yields were higher under grazing. The difference between perennial ryegrass yield in monoculture and in mixture was variable. In the second harvest year, a significant interaction effect was seen between management and white clover variety for white clover yield but not for perennial ryegrass yield. The relationship between clover yield and grass yield differed between the two management regimes. Under cutting, a negative correlation was observed, indicative of competitive effects. However, under grazing, no such correlation was seen. Possible mechanisms underlying these outcomes are discussed. [source] A joint study based on the electron localization function and catastrophe theory of the chameleonic and centauric models for the Cope rearrangement of 1,5-hexadiene and its cyano derivativesJOURNAL OF COMPUTATIONAL CHEMISTRY, Issue 14 2005Victor Polo Abstract A novel interpretation of the chameleonic and centauric models for the Cope rearrangements of 1,5-hexadiene (A) and different cyano derivatives (B: 2,5-dicyano, C: 1,3,4,6-tetracyano, and D: 1,3,5-tricyano) is presented by using the topological analysis of the electron localization function (ELF) and Thom's catastrophe theory (CT) on the reaction paths calculated at the B3LYP/6-31G(d,p) level. The progress of the reaction is monitorized by the changes of the ELF structural stability domains (SSD), each being change controlled by a turning point derived from CT. The reaction mechanism of the parent reaction A is characterized by nine ELF SSDs. All processes occur in the vicinity of the transition structure and corresponding to a concerted formation/breaking of C1C6 and C3C4 bonds, respectively, together with an accumulation of charge density onto C2 and C5 atoms. Reaction B presents the same number of ELF SSDs as A, but a different order appears; the presence of 2,5-dicyano substituents favors the formation of C1C6 bonds over the breaking of C3C4 bond process, changing the reaction mechanism from a concerted towards a stepwise, via a cyclohexane biradical intermediate. On the other side, reaction C presents the same type of turning points but two ELF SSD less than A or B; there is an enhancement of the C3C4 bond breaking process at an earlier stage of the reaction by delocalizing the electrons from the C3C4 bond among the cyano groups. In the case of competitive effects of cyano subsituents on each moiety, as it is for reaction D, seven different ELF SSDs have been identified separated by eight turning points (two of them occur simultaneously). Both processes, formation/breaking of C1C6 and C3C4 bonds, are slightly favored with respect to the parent reaction (A), and the TS presents mixed electronic features of both B and C. The employed methodology provides theoretical support for the centauric nature (half-allyl, half-radical) for the TS of D. © 2005 Wiley Periodicals, Inc. J Comput Chem 26: 1427,1437, 2005 [source] Above- versus below-ground competitive effects and responses of a guild of temperate tree speciesJOURNAL OF ECOLOGY, Issue 1 2009K. David Coates Summary 1The neutral theory debate has highlighted the scarcity of robust empirical estimates of the magnitude of competitive effects and responses within guilds of co-occurring tree species. Our analysis quantifies the relative magnitude of all possible pairwise competitive interactions within a guild of nine co-occurring tree species in temperate forests of northern, interior British Columbia, and explicitly partitions the competitive effects of neighbours into the effects of shading versus the residual effects of ,crowding', assumed to reflect below-ground competition. 2Models that treated neighbours as equivalent in their competitive effects were the most parsimonious for the five species with the smallest sample sizes. For the remaining species (samples sizes of > 150 individuals), the best models estimated separate competition coefficients for all nine species of neighbours. We take this as evidence that species do indeed differ in their competitive effects, but that there can be a minimum sample size required to discriminate between them. 3There was a strong size-dependency in potential growth. Six species showed an optimal growth at a size between 5 and 20 cm diameter. Potential growth declined moderately to strongly as diameter increased. Sensitivity to crowding varied as a function of tree size for five of the nine species; however, this response was not consistent by tree species. 4The magnitude of reduction in growth due to crowding was greater on average than the reduction in growth due to shading, except for the two least shade tolerant conifers. Sensitivity to shading among the conifer species was correlated with their shade tolerance. 5The per capita effects of crowding by different species of neighbours varied widely. A large number of the estimated pairwise per capita competition coefficients were very low. The relative magnitude of the strength of intra- versus interspecific competition also varied widely among the tree species. 6Synthesis. Model selection techniques effectively separated above- and below-ground competition in complex forests, and allowed us to assess differences among species in competitive effects and responses. While below-ground effects were strong, they were due to proximity of neighbours from a very specific (and small) subset of strong competitors within the guild. Response to crowding varied with tree size but the nature of the relationship varied widely among the species. [source] Competitive effects of grasses and woody plants in mixed-grass prairieJOURNAL OF ECOLOGY, Issue 4 2001Duane A. Peltzer Summary 1,Variation in the competitive ability of plant species may determine their persistence and abundance in communities. We quantified the competitive effects of grasses and woody plants in native mixed-grass prairie on the performance of transplant species and on resources. 2,We separated the effects of grasses, shrubs and intact vegetation containing both grasses and shrubs by manipulating the natural vegetation using selective herbicides to create four neighbourhood treatments: no neighbours (NN), no shrubs (NS), no grasses (NG) and all neighbours (AN). Treatments were applied to 2 × 2 m experimental plots located in either grass- or shrub-dominated habitats. The effects of grasses and shrubs on resource availability (light, soil moisture, soil available nitrogen) and on the growth of transplants of Bouteloua gracilis, a perennial tussock grass, and Elaeagnus commutata, a common shrub, were measured over two growing seasons. 3,Resource availability was two- to fivefold higher in no neighbour (NN) plots than in vegetated plots (NS, NG, AN) with grasses and shrubs having similar effects. Light penetration declined linearly with increasing grass or shrub biomass, to a minimum of about 30% incident light at 500 g m,2 shoot mass. Soil resources did not decline with increasing neighbour shoot or root mass for either grasses or shrubs, suggesting that the presence of neighbours was more important than their abundance. 4,Transplant growth was significantly suppressed by the presence of neighbours, but not by increasing neighbour shoot or root biomass, except for a linear decline in Bouteloua growth with increasing neighbour shoot mass in plots containing only shrubs. Competition intensity, calculated as the reduction in transplant growth by neighbours, was similar in both grass- and shrub-dominated habitats for transplants of Bouteloua, but was less intense in shrub-dominated habitats for the shrub Elaeagnus. Variation in the persistence and abundance of plants in communities may therefore be more strongly controlled by variation in the competitive effects exerted by neighbours than by differences in competitive response ability. [source] The relationship of total and per-gram rankings in competitive effect to the natural abundance of herbaceous perennialsJOURNAL OF ECOLOGY, Issue 1 2001Timothy G. Howard Summary 1,Using a field experiment and a garden experiment, I estimated the rankings in total and per-gram competitive effect of non-woody perennial old-field species. 2,Total competitive effects were defined as the relative reduction in growth of a target from no-neighbour to with-neighbour conditions. Per-gram competitive effects were defined as the per-unit relative reduction in target growth among increasing neighbour densities, and were determined from the shape of a nonlinear curve fit through a distribution of normalized target performance against neighbour mass. 3,In both experiments, mean total competitive effect differed significantly among species, indicating a strong competitive hierarchy. In the garden experiment only species at opposite ends of the ranking differed significantly in per-gram competitive effect, resulting in a weaker competitive hierarchy based on this measure. 4,Nonetheless, rankings of per-gram competitive effect were more strongly correlated with rank in abundance than were rankings of total competitive effect. 5,Per-gram competitive effect may be more predictive of natural abundance than total competitive effect for at least two reasons. The effects of neighbour abundance on targets are nonlinear, and unlike total effects, per-gram estimates of competitive effect may therefore indicate how competition changes over time with changing neighbour densities. Also, if higher per-gram competitive effect reflects higher per-unit nutrient uptake rates, it would probably be advantageous to a species throughout the individual's life span, rather than only when the individual is larger than its surrounding neighbours. [source] Effect of lianas on tree regeneration in gaps and forest understorey in a tropical forest in GhanaJOURNAL OF VEGETATION SCIENCE, Issue 5 2008T. Toledo-Aceves Abstract Questions: Do lianas alter the relative success of tree species during regeneration? Are the effects of lianas on tree seedlings moderated by canopy openness? How are patterns of biomass allocation in tree seedlings affected by liana competition? Location: Tropical moist semi-deciduous forest in Ghana. Methods: Seedlings of the trees Nauclea diderrichii (pioneer), Khaya anthotheca (non-pioneer light demander) and Garcinia kola (non-pioneer shade bearer) were planted with the lianas Acacia kamerunensis (fast growing) and Loeseneriella rowlandii (slow growing) in large and small gaps (ca. 15% and 8% PAR respectively) and in the forest understorey (ca. 4% PAR). Seedling survival, growth and biomass allocation were measured. Results: Canopy openness moderated the interaction between liana and tree seedlings. The nature of the interaction was both liana and tree species specific and displayed temporal variation. Acacia competition effects were stronger in sites with greater canopy openness. In big gaps, Acacia reduced significantly the biomass of Nauclea by 32% and Khaya by about 50%. Khaya growth in leaf area was five times greater without Acacia, while Nauclea and Garcinia were not affected. Acacia was more plastic than Loeseneriella in response to the environment and the tree species. Our results show that while Loeseneriella, with lower rates of growth, did not affect seedling growth of the three species evaluated, Acacia could alter the relative success of tree species during regeneration. Conclusions: There is evidence that competitive effects by Acacia on tree regeneration through competition could modify tree species capacity to establish. Effects by lianas at the regeneration phase may have important implications for forest management. [source] Do pollen carryover and pollinator constancy mitigate effects of competition for pollination?OIKOS, Issue 7 2009Benjamin R. Montgomery Pollinator constancy and pollen carryover are both thought to mitigate competitive effects that result when shared pollinators cause loss of pollen to heterospecific flowers. I present analytical and simulation models to investigate how pollinator constancy and pollen carryover interact with each other and with the relationship between pollen receipt and seed set to determine pollination success in competitive environments. With inconstant pollinators, increased pollen carryover reduces variance in pollen receipt without affecting average pollen receipt. Consequently, for flowers requiring at least a threshold quantity of pollen for success, rare flowers with inconstant pollinators benefit from reduced carryover, especially for high pollen receipt thresholds, whereas common flowers benefit from increased carryover, especially for low receipt thresholds. Pollinator constancy is predicted to increase pollen receipt, especially if pollen carryover rates are low. As a result, increased pollinator constancy reduces the range of pollen receipt thresholds for which carryover is beneficial. Similarly, for flowers whose pollination success is a convex function of pollen receipt, carryover is expected to increase fecundity if pollinators are inconstant, but with even a low degree of pollinator constancy, carryover reduces fecundity. These results predict that rare plants with many ovules per flower benefit from dispersing aggregations of pollen, especially if their pollinators exhibit constancy, whereas plants with inconstant pollinators and low thresholds of pollen receipt benefit from pollen grains dispersing individually to increase the number of flowers reached by the pollen. [source] Shoot herbivory on the invasive plant, Centaurea maculosa, does not reduce its competitive effects on conspecifics and nativesOIKOS, Issue 3 2006Beth A. Newingham Herbivory can have negative, positive, or no effect on plants. However, insect biological control assumes that herbivory will negatively affect the weed and release natives from competition. Centaurea maculosa, an invader in North America, is tolerant to herbivory, and under some conditions, herbivory may increase its competitive effects on natives. Therefore, we investigated two hypotheses: 1) herbivory stimulates compensatory growth by C. maculosa, which increases its competitive effects, and 2) herbivory stimulates the allelopathic effect of C. maculosa. In the greenhouse, Trichoplusia ni shoot herbivory reduced C. maculosa biomass when shoot damage exceeded 40% of the total original leaf area. Conspecific neighbors had no effect on C. maculosa biomass, and the presence of the natives Festuca idahoensis and F. scabrella had a positive effect on C. maculosa. Neighbors did not alter the effects of shoot herbivory. More importantly, even intense shoot herbivory on C. maculosa did not benefit neighboring plants. In a field experiment, clipping 50% of C. maculosa aboveground biomass in the early summer and again in the late summer reduced final biomass by 40% at the end of the season; however, this clipping did not affect total biomass production or reproductive output. Festuca idahoensis neighbors did not increase the effects of clipping, and aboveground damage to C. maculosa did not release F. idahoensis from competition. In the greenhouse we used activated carbon to adsorb allelochemicals, which reduced the competitive effects of C. maculosa on F. idahoensis but not on F. scabrella or other C. maculosa. However, we found no increase in the allelopathic effects of C. maculosa after shoot herbivory. In summary, our results correspond with others indicating that exceptionally high intensities of herbivory are required to suppress C. maculosa growth and reproduction; however, even intense herbivory on C. maculosa does not insure that native bunchgrasses will benefit. [source] Detecting the effects of introduced species: a case study of competition between Apis and BombusOIKOS, Issue 3 2006Diane M. Thomson Developing tools for rapid assessment of introduced species impacts is one of the most important challenges in invasion ecology. Most assessments of impact rely on correlational data or other indirect measures. Yet few studies have evaluated invasion effects using multiple, simultaneously applied monitoring and experimental approaches, in order to compare easily obtained metrics with more difficult but direct measures of reproductive success or population dynamics. In this study, I use data from an experimental test of introduced honey bee (Apis mellifera) impacts on native bumble bees (Bombus spp.) to address two major questions: 1) how well did observational data on niche overlap and spatial correlations between Apis and Bombus predict the results of experimental tests of competitive effects? and 2) how well did effects of the experimental Apis manipulations on Bombus foragers, which are easy to observe, predict changes in reproductive success of colonies, which are difficult to measure? Niche overlap between Apis and Bombus varied substantially, but increased to levels as high as 80,90% during periods of resource scarcity. Correlations between numbers of Apis foragers and numbers of Bombus foragers were also highly variable, but I detected a significant negative relationship in only one of the seven months observed. In contrast, the experimental results showed that mean numbers of Bombus foragers observed on a given transect increased significantly with greater distance from introduced Apis colonies. Of these three measures (niche overlap, correlations in abundances, and effects of experimental introductions), only the experimental data on forager abundances accurately estimated competitive effects on colony reproductive success previously reported for the same experiment, and the correlational data in particular completely failed to predict the effects observed in the experimental study. This work suggests that great caution is warranted in making assessments of invasion impact on the basis of spatial or temporal correlations between invasive and native species. Thus, investing in even small and limited experimental studies may be more valuable than extensive observational work in quantifying invasion impacts. [source] Interspecific and intraspecific interactions between salt marsh plants: integrating the effects of environmental factors and density on plant performanceOIKOS, Issue 2 2002Jonathan M. Huckle There has been much debate about the role of plant interactions in the structure and function of vegetation communities. Here the results of a pot experiment with controlled environments are described where three environmental variables (nutrients, sediment type and waterlogging) were manipulated factorially to identify their effects on the growth and intensity of interactions occurring between Spartina anglica and Puccinellia maritima. The two species were grown in split-plot planting treatments, representing intraspecific and interspecific addition series experiments, to determine individual and interactive effects of environmental factors and plant interactions on plant biomass. Above-ground growth of both species involved interactions between the environmental and planting treatments, while below-ground, environmental factors affected the biomass irrespective of planting treatments. It was suggested that this difference in growth response is evidence that in our experiment plant interactions between the two species occur primarily at the above-ground level. The intensity of plant interactions varied in a number of ways. First, interactions between Spartina and Puccinellia were distinctly asymmetrical, Puccinellia exerting a competitive effect on Spartina, with no reciprocal effect, and with a facilitative effect of Spartina on Puccinellia in low nutrient conditions. Second, the interactions varied in intensity in different environmental conditions. Interspecific competitive effects of Puccinellia on Spartina were more intense in conditions favourable to growth of Puccinellia and reduced or non-existent in environments with more abiotic stress. Third, intraspecific competition was found to be less intense for both species than interspecific interactions. Finally, the intensity of plant interactions involving both species was more intense above ground than below ground, with a disproportionate reduction in the intensity of interspecific competition below relative to above ground in treatments with less productive sediments and greater immersion. This is interpreted as reflecting a potential mechanism by which Spartina may be able to evade competitive neighbours. [source] Picking battles wisely: plant behaviour under competitionPLANT CELL & ENVIRONMENT, Issue 6 2009ARIEL NOVOPLANSKY ABSTRACT Plants are limited in their ability to choose their neighbours, but they are able to orchestrate a wide spectrum of rational competitive behaviours that increase their prospects to prevail under various ecological settings. Through the perception of neighbours, plants are able to anticipate probable competitive interactions and modify their competitive behaviours to maximize their long-term gains. Specifically, plants can minimize competitive encounters by avoiding their neighbours; maximize their competitive effects by aggressively confronting their neighbours; or tolerate the competitive effects of their neighbours. However, the adaptive values of these non-mutually exclusive options are expected to depend strongly on the plants' evolutionary background and to change dynamically according to their past development, and relative sizes and vigour. Additionally, the magnitude of competitive responsiveness is expected to be positively correlated with the reliability of the environmental information regarding the expected competitive interactions and the expected time left for further plastic modifications. Concurrent competition over external and internal resources and morphogenetic signals may enable some plants to increase their efficiency and external competitive performance by discriminately allocating limited resources to their more promising organs at the expense of failing or less successful organs. [source] Grasshopper Herbivory Affects Native Plant Diversity and Abundance in a Grassland Dominated by the Exotic Grass Agropyron cristatumRESTORATION ECOLOGY, Issue 1 2009David H. Branson Abstract The indirect effects of native generalist insect herbivores on interactions between exotic and native grassland plants have received limited attention. Crested wheatgrass (Agropyron cristatum) is the most common exotic rangeland grass in western North America. Crested wheatgrass communities are resistant to colonization by native plant species and have strong competitive effects on native species, imposing problems for the restoration of native grasslands. Grasshoppers are generalist herbivores that are often abundant in Crested wheatgrass,dominated sites in the northern Great Plains. We conducted two experiments in a Crested wheatgrass,dominated grassland in western North Dakota to test the hypothesis that grasshopper herbivory influences local Crested wheatgrass community composition by impeding native seedlings. Grasshopper herbivory negatively affected the species richness, abundance, and Shannon diversity of native plants in 3 of 4 years. Although additional research is needed to determine if grasshoppers actively select native plants, the effects of grasshopper herbivory may be an important consideration in the restoration of Crested wheatgrass areas. Our findings illustrate the importance of understanding the impact of native generalist invertebrate herbivores on the relationships between exotic and native plants. [source] INDUSTRY EFFECTS OF ANALYST STOCK REVISIONSTHE JOURNAL OF FINANCIAL RESEARCH, Issue 2 2006Aigbe Akhigbe Abstract We examine the industry valuation effects of analyst stock revisions and identify the variables that influence these effects. Our results show that industry rivals experience significant abnormal returns in response to revision announcements. Although the mean stock price response suggests contagion effects, there is also evidence of significant competitive effects. The valuation effects are influenced by the magnitude of the rated firm's announcement return, along with analyst-specific and industry-specific characteristics. However, the sensitivity of the valuation effects to these characteristics is conditioned on whether the industry effects are contagious or competitive. [source] Differentiation and Competition in HMO MarketsTHE JOURNAL OF INDUSTRIAL ECONOMICS, Issue 4 2003David Dranove This paper examines how differentiation among Health Maintenance Organizations (HMOs) affects local market competition. Most markets for HMOs appear sufficiently unconcentrated; however, differences among HMOs may make competition less intense than the number of competitors would suggest. To investigate this possibility, we distinguish HMOs that serve only local markets from those that operate regional or national networks. We analyze how HMOs of one type affect the profitability of the other using an equilibrium model of entry and product choice. While the two types of HMOs have strong competitive effects within segments, the competitive effect of differentiated firms is negligible. [source] Upfront payments and exclusion in downstream marketsTHE RAND JOURNAL OF ECONOMICS, Issue 3 2007Leslie M. Marx Although upfront payments are often observed in contracts between manufacturers and retailers, little is known about their competitive effects or the role retailers play in securing them. In this article, we consider a model in which two competing retailers make take-it-or-leave-it offers to a common manufacturer. We find that upfront payments are a feature of equilibrium contracts, and in all equilibria, only one retailer buys from the manufacturer. These findings support the claims of small manufacturers who argue that they are often unable to obtain widespread distribution for their products because of upfront payments. [source] Impacts of hive honeybees on Tasmanian leatherwood Eucryphia lucida Labill. (Eucryphiaceae)AUSTRAL ECOLOGY, Issue 2 2009STEPHEN A. MALLICK Abstract Despite honeybees (Apis mellifera L.) occurring as a feral and commercially managed species in many parts of Australia, the effects of honeybees on native Australian ecosystems are poorly understood. We examined the impacts of honeybee apiaries on Tasmanian Leatherwood Eucryphia lucida Labill. (Eucryphiaceae) by comparing commercial apiary sites with control sites >2 km from the nearest apiary. Feral honeybees were common at control sites (73% of honeybees feral) but were scarce at apiary sites (2%), and hive honeybees appeared to be competitively displacing feral honeybees near apiaries. Visit rates by native insects appeared to be un-affected by the increased numbers of hive honeybees near apiaries. Standing crops of nectar sugar were significantly depressed at apiary sites. Pollen was rapidly removed from flowers at apiary sites resulting in full separation of the male and female flower-phases (flowers completely dichogamous). In contrast, at control sites, pollen tended to remain in flowers into the female phase (flowers partially dichogamous). There was no difference in the total number of pollen grains deposited on stigmas or in percentage seed set among apiary and control sites. However, fruit set was elevated at apiary sites, possibly owing to reduced autonomous (within-flower) selfing. Our study indicated that honeybees significantly reduce floral resources (nectar and pollen) around apiaries, although any competitive effects on native insects may have been obscured by large variation in the abundance of native insects among experimental sites. [source] Evaluating the role of the dingo as a trophic regulator in Australian ecosystemsAUSTRAL ECOLOGY, Issue 5 2007A. S. GLEN Abstract The importance of strongly interactive predators has been demonstrated in many ecosystems, and the maintenance or restoration of species interactions is a major priority in the global conservation of biodiversity. By limiting populations of prey and/or competitors, apex predators can increase the diversity of systems, often exerting influences that cascade through several trophic levels. In Australia, emerging evidence points increasingly towards the dingo (Canis lupus dingo) as a strongly interactive species that has profound effects on ecosystem function. Through predatory and competitive effects, dingoes can alter the abundance and function of mesopredators including the introduced red fox (Vulpes vulpes) and feral cat (Felis catus), and herbivores including the European rabbit (Oryctolagus cuniculus). These effects often benefit populations of native prey, and diversity and biomass of vegetation, but may not occur under all circumstances. For example, the social structure of dingoes is of great importance; a pack subject to minimal human interference regulates its own numbers, and such packs appear to have fewer undesirable impacts such as predation on livestock. Despite abundant observational evidence that the dingo is a strong interactor, there have been few attempts to test its ecological role experimentally. Given the well-recognized importance of species interactions to ecosystem function, it is imperative that such experiments be carried out. To do this, we propose three broad questions: (i) do dingoes limit the abundance of other predators or prey? (ii) do dingoes affect the ecological relationships of other predators or prey (e.g. by altering their spatial or temporal activity patterns)? and (iii) does the removal or reintroduction of dingoes entrain ecological cascades? Finally, we discuss the design of appropriate experiments, using principles that may also be applied to investigate species interactions on other continents. Research might seek to clarify not only the impacts of dingoes at all trophic levels, but also the mechanisms by which these impacts occur. [source] | |||||||||||||||||||