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Kinds of Plot Data Selected AbstractsInvasion impacts local species turnover in a successional systemECOLOGY LETTERS, Issue 9 2004Kathryn A. Yurkonis Abstract Exotic plant invasions are often associated with declines in diversity within invaded communities. However, few studies have examined the local community dynamics underlying these impacts. Changes in species richness associated with plant invasions must occur through local changes in extinction and/or colonization rates within the community. We used long-term, permanent plot data to evaluate the impacts of the exotic vine Lonicera japonica. Over time, species richness declined with increasing L. japonica cover. L. japonica reduced local colonization rates but had no effect on extinction rates. Furthermore, we detected significant reductions in the immigration of individual species as invasion severity increased, showing that some species are more susceptible to invasion than others. These findings suggest that declines in species richness associated with L. japonica invasion resulted from effects on local colonization rates only and not through the competitive displacement of established species. [source] Net primary productivity mapped for Canada at 1-km resolutionGLOBAL ECOLOGY, Issue 2 2002J Liu Abstract Aim To map net primary productivity (NPP) over the Canadian landmass at 1-km resolution. Location Canada. Methods A simulation model, the Boreal Ecosystem Productivity Simulator (BEPS), has been developed. The model uses a sunlit and shaded leaf separation strategy and a daily integration scheme in order to implement an instantaneous leaf-level photosynthesis model over large areas. Two key driving variables, leaf area index (every 10 days) and land cover type (annual), are derived from satellite measurements of the Advanced Very High Resolution Radiometer (AVHRR). Other spatially explicit input data are also prepared, including daily meteorological data (radiation, precipitation, temperature, and humidity), available soil water holding capacity (AWC) and forest biomass. The model outputs are compared with ground plot data to ensure that no significant systematic biases are created. Results The simulation results show that Canada's annual net primary production was 1.22 Gt C year,1 in 1994, 78% attributed to forests, mainly the boreal forest, without considering the contribution of the understorey. The NPP averaged over the entire landmass was ~140 g C m,2 year,1 in 1994. Geographically, NPP varied greatly among ecozones and provinces/territories. The seasonality of NPP is characterized by strong summer photosynthesis capacities and a short growing season in northern ecosystems. Conclusions This study is the first attempt to simulate Canada-wide NPP with a process-based model at 1-km resolution and using a daily step. The statistics of NPP are therefore expected to be more accurate than previous analyses at coarser spatial or temporal resolutions. The use of remote sensing data makes such simulations possible. BEPS is capable of integrating the effects of climate, vegetation, and soil on plant growth at a regional scale. BEPS and its parameterization scheme and products can be a basis for future studies of the carbon cycle in mid-high latitude ecosystems. [source] Invasion impacts diversity through altered community dynamicsJOURNAL OF ECOLOGY, Issue 6 2005KATHRYN A. YURKONIS Summary 1Invading plant species often alter community structure, composition and, in some instances, reduce local diversity. However, the community dynamics underlying these impacts are relatively unknown. 2Declines in species richness with invasion may occur via displacement of resident species and/or reduction of seedling establishment by the invader. These two mechanisms differ in the demographic stage of the interaction. 3We document turnover dynamics using long-term permanent plot data to assess the mechanism(s) of invasion impacts of four exotic species on a mixed community of native and exotic species. These mechanisms were evaluated at both the neighbourhood (1-m2 plot) and population (individual species) scales. 4During invasion, species richness declined with increasing invader cover for three of the four invaders. All invaders reduced colonization rates, but had no effect on extinction rates at the neighbourhood scale. Populations differed in their susceptibility to invasion impacts, with significant reductions in colonization for 10 of 25 (40%) species and increases in extinction for only 4 of 29 (14%) species. 5At neighbourhood and population scales, influences of invasion on community dynamics were essentially the same for all invaders regardless of life-form. While individual resident species had some increase in extinction probability, community richness impacts were largely driven by colonization limitation. 6The consistency of invasion impacts across life-forms suggests establishment limitation as a general mechanism of invasion impact. This common causal mechanism should be explored in other systems to determine the extent of its generality. [source] The genetic and economic impact of the CIMMYT wheat breeding program on local producers in the Yaqui Valley, Sonora MexicoAGRICULTURAL ECONOMICS, Issue 5 2010Lawton L. Nalley CIMMYT; Public wheat breeding; Economic impact of technological change Abstract This article quantifies the productivity gain from CIMMYT-released semidwarf bread wheat (Triticum aestivum) cultivars over time, using test plot data from Mexico's Yaqui Valley. Previous studies have shown a deceleration in irrigated wheat yield growth since the 1980s, which could be due to slowing increase in genetic potential. Our results suggest that CIMMYT cultivars contributed a 0.46% annual increase (about 38 kg/ha annually) to wheat yields in the Yaqui Valley, which raised local wheat producers' revenue by an average of $4 million annually for the period 1990 to 2002, and by approximately $9 million in 2002. [source] Seed size and response to rainfall patterns in annual grasslands: 16 years of permanent plot dataJOURNAL OF VEGETATION SCIENCE, Issue 1 2009B. Peco Abstract Question: Are seed size and plant size linked to species responses to inter-annual variations in rainfall and rainfall distribution during the growing season in annual grasslands? Location: A 16-year data set on species abundance in permanent plots 15 km north of Madrid in a Quercus ilex subsp. ballota dehesa. Methods: At species level, a GLM was used to analyse the effects of various rainfall indices (total autumn rainfall, early autumn rainfall and spring drought) on species abundance residuals with respect to time and topography. We also assessed the importance of seed size and plant size in the species responses at community level using species as data points. Seed mass and maximum stem length were used as surrogates for seed size and plant size, respectively. Results: Seed mass and plant size may explain some of the fluctuations in the floristic composition of annual species associated with autumn rainfall patterns. Species that are more abundant in dry autumns have greater seed mass than those species that are more abundant in wet autumns. Early autumn rainfall seems to favour larger plants. Conclusions: Our empirical results support the hypothesis that autumn rainfall patterns affect the relative establishment capacity of small and large seedlings in annual species. [source] On a level field: the utility of studying native and non-native species in successional systemsAPPLIED VEGETATION SCIENCE, Issue 1 2009Scott J. Meiners Abstract Questions: How do successional systems contribute to our understanding of plant invasions? Why is a community-level approach important in understanding invasion? Do native and non-native plant species differ in their successional trajectories within communities? Location: Northeastern United States, in the Piedmont region of New Jersey. Previously farmed since the 1700s, ten fields were experimentally retired from agriculture beginning in 1958. Methods: Fifty years of permanent plot data were used to quantify the population demographics of the 84 most abundant species during succession. These measures were then used to compare native, non-native and non-native invasive species' population dynamics in succession. Results: Once basic life-history characteristics were accounted for, there were no differences in the population dynamics of native, non-native, and non-native invasive plant species. However, the species pool in this study was biased towards ruderal species, which largely constrained non-native species to early succession. Conclusion: Successional systems are crucial to our understanding of invasions as they constrain all species to the role of colonizer. By focusing on the whole community, rather than on individual problematic species, we found no systematic differences between native and non-native species. Thus, knowing simple life-history information about a species would be much more useful in setting management priorities than where the species originated. [source] | |||||||||||||