106 research outputs found

    Biochar and Managed Perennial Ecosystems

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    Biochar is a carbon-rich material that is similar to charcoal. It is produced when biomass is burned in the absence of oxygen, a process otherwise known as pyrolysis. Pyrolysis and the production of biochar are currently being promoted as a means to both produce domestic fuel (bio-oil) while concurrently producing a co-product that increases crop yield and sequesters carbon in the soil (biochar). While there may be many potential benefits in the application of biochar to agricultural soils, such as enhanced soil fertility and improved soil water status, there are no studies of higher-order ecological and ecosystem effects of biochar and its potential synergistic interactions (either positive or negative) on complex perennial systems. The goal of this field experiment is to determine how biochar and manure addition directly affect ecosystem structure and function in perennial systems, specifically soil nutrients, water, plants, and soil organisms

    Biochar and Managed Perennial Ecosystems: Testing for Synergy in Ecosystem Function and Biodiversity

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    Biochar is a carbon-rich material that is similar to charcoal. It is produced when biomass is burned in the absence of oxygen, a process otherwise known as pyrolysis. Pyrolysis and the production of biochar are currently being promoted as a means to both produce domestic fuel (biooil) and concurrently producing a co-product that increases crop yield and sequesters carbon in the soil (biochar). While there may be many potential benefits in the application of biochar to agricultural soils, such as enhanced soil fertility and improved soil water status, there are no studies of higher-order ecological and ecosystem effects of biochar and its potential synergistic interactions (either positive or negative) on complex perennial systems. The goal of this field experiment is to determine how biochar and manure addition directly affect ecosystem structure and function in perennial systems, specifically soil nutrients, water, plants, and soil organisms

    Spatial heterogeneity in species composition constrains plant community responses to herbivory and fertilisation

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    Environmental change can result in substantial shifts in community composition. The associated immigration and extinction events are likely constrained by the spatial distribution of species. Still, studies on environmental change typically quantify biotic responses at single spatial (time series within a single plot) or temporal (spatial beta diversity at single time points) scales, ignoring their potential interdependence. Here, we use data from a global network of grassland experiments to determine how turnover responses to two major forms of environmental change – fertilisation and herbivore loss – are affected by species pool size and spatial compositional heterogeneity. Fertilisation led to higher rates of local extinction, whereas turnover in herbivore exclusion plots was driven by species replacement. Overall, sites with more spatially heterogeneous composition showed significantly higher rates of annual turnover, independent of species pool size and treatment. Taking into account spatial biodiversity aspects will therefore improve our understanding of consequences of global and anthropogenic change on community dynamics

    Nematode community development early in ecological restoration: The role of organic amendments

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    a b s t r a c t Soil food web structure is an integral component of ecosystem function, but there are few strategies orientated towards managing its development in restoration projects. The objective of this study was to direct nematode community structure and function through the application of organic amendments to the soil of an urban landfill remediation project using native grassland vegetation. We used a 2 Â 3 factorial design in which an organic amendment was added to the soil at different locations (incorporated versus surface-applied) and amounts (none, light, heavy). Nematode and plant community structure were monitored over three growing seasons to determine the rate and direction of change. Surface application of organic amendments supported greater grass and total plant densities compared to incorporated amendment treatments, but plant density did not vary with amendment amount. Total nematode density, family diversity and family richness were not affected by the amendment treatments, but both family richness and seasonal nematode density increased over the duration of the experiment. Other descriptors of nematode community development (Structure, Maturity, and Plant Parasite Indexes) were not influenced by either amendment amount or location, but varied significantly over time. Contrary to expectations, the surface amendment treatments significantly increased bacterivorous, plant parasitic, omnivorous and predator nematode densities, but had no influence on fungi/root-tip feeding nematodes. Also contrary to our hypotheses, the surface treatments had smaller Channel Index and greater Enrichment Index values relative to the incorporated treatments during the first 15 month of the experiment. We hypothesize that the surface amendments are indirectly affecting the structure of the nematode community by promoting greater plant density, thus increasing the concentration of highquality organic matter (such as root exudates) in the soil. This promotes the development of a nematode community dominated by opportunistic groups that respond rapidly to increased resource availability. Future studies should aim to distinguish between the organic amendment's direct function as a potential food source for the soil biota versus their indirect role as an environmental variable, including their capability to alter the availability of plant-derived resources

    Nutrient addition shifts plant community composition towards earlier flowering species in some prairie ecoregions in the U.S. Central Plains

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    e0178440, 15 p.The distribution of flowering across the growing season is governed by each species' evolutionary history and climatic variability. However, global change factors, such as eutrophication and invasion, can alter plant community composition and thus change the distribution of flowering across the growing season. We examined three ecoregions (tall-, mixed, and short-grass prairie) across the U.S. Central Plains to determine how nutrient (nitrogen (N), phosphorus, and potassium (+micronutrient)) addition alters the temporal patterns of plant flowering traits. We calculated total community flowering potential (FP) by distributing peakseason plant cover values across the growing season, allocating each species' cover to only those months in which it typically flowers. We also generated separate FP profiles for exotic and native species and functional group. We compared the ability of the added nutrients to shift the distribution of these FP profiles (total and sub-groups) across the growing season. In all ecoregions, N increased the relative cover of both exotic species and C3 graminoids that flower in May through August. The cover of C4 graminoids decreased with added N, but the response varied by ecoregion and month. However, these functional changes only aggregated to shift the entire community's FP profile in the tall-grass prairie, where the relative cover of plants expected to flower in May and June increased and those that flower in September and October decreased with added N. The relatively low native cover in May and June may leave this ecoregion vulnerable to disturbance induced invasion by exotic species that occupy this temporal niche. There was no change in the FP profile of the mixed and short-grass prairies with N addition as increased abundance of exotic species and C3 graminoids replaced other species that flower at the same time. In these communities a disturbance other than nutrient addition may be required to disrupt phenological patterns

    More salt, please:global patterns, responses, and impacts of foliar sodium in grasslands

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    Sodium is unique among abundant elemental nutrients, because most plant species do not require it for growth or development, whereas animals physiologically require sodium. Foliar sodium influences consumption rates by animals and can structure herbivores across landscapes. We quantified foliar sodium in 201 locally abundant, herbaceous species representing 32 families and, at 26 sites on four continents, experimentally manipulated vertebrate herbivores and elemental nutrients to determine their effect on foliar sodium. Foliar sodium varied taxonomically and geographically, spanning five orders of magnitude. Site‐level foliar sodium increased most strongly with site aridity and soil sodium; nutrient addition weakened the relationship between aridity and mean foliar sodium. Within sites, high sodium plants declined in abundance with fertilisation, whereas low sodium plants increased. Herbivory provided an explanation: herbivores selectively reduced high nutrient, high sodium plants. Thus, interactions among climate, nutrients and the resulting nutritional value for herbivores determine foliar sodium biogeography in herbaceous‐dominated systems
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