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58 results for “nutrient additions”
CSASN TASCC Nutrient additions to streams near Toolik Field Sation, Alaska 2010 to 2012
The Changing Seasonality of Artic Stream Systems (CSASN) was active from 2010 to 2012. The CSASN goal was to quantify the relative influences of throughflow, lateral inputs, and hyporheic regeneration on the seasonal fluxes C, N, and P in an arctic river network, and to determine how these influences might shift under seasonal conditions that are likely to be substantially different in the future. There were a number of TASCC and Plateau nutrient additions at each sampling location. The data in this file contains nutrient uptake values from each sampling event during each TASCC and Plateau addtion during the CSASN project.
Long-term changes in tundra carbon balance following wildfire, climate change and potential nutrient addition, a modeling analysis.
A study investigating the mechanisms that control long-term response of tussock tundra to fire and to increases in air temperature, CO2, nitrogen deposition and phosphorus weathering. The MBL MEL was used to simulate the recovery of three types of tussock tundra, unburned, moderately burned, and severely burned in response to changes in climate and nutrient additions. The simulations indicate that the recovery of nutrients lost during wildfire is difficult under a warming climate because warming increases nutrient cycles and subsequently leaching within the ecosystem. The study was published in Ecological Applications (in press, 2016). This dataset is the long term archive of the results published in the paper. The full dataset has been broken into two parts because of the number and size of the files. Part 1 contains MBL MEL executable, a model description file in word, and the input files to run the simulations. Part 2 contains the output files for all simulations. Both Part 1 and Part 2 contain several different types of files. In Part 1 the comma separated ascii file included with the dataset is one of the many driver files used for the simulations. The variable descriptions below describe the variables in that file and all the driver files. In Part 2 the comma separated ascii file included with the dataset is one of the many output files from the simulations. The variable descriptions below describe the variables in that file and all the output files. To access all the files in the dataset be sure to download the two zip files described in the Methods section below. Note that the full download is large, over 700 MB for each part. Permanent Archive of the data published in Jiang, et al., in press, Modeling long-term changes in tundra carbon balance following wildfire, climate change and potential nutrient addition, Ecological Applications.
Interior Alaska managed sites: soil organic layer and mineral soil nutrient concentrations and additional characteristics measured one time in either summer 2012 or 2013
This dataset contains soil organic layer and mineral soil depth, C and N concentrations, and other soil characteristics collected at all managed and adjacent unmanaged study sites.
McMurdo Dry Valleys LTER: Nutrient addition incubation experiments using sediments from supraglacial streams in Taylor Valley, Antarctica, December 2017
We used sediment incubations to quantify and compare nutrient uptake rates from biota living in sediment across glaciers in Taylor Valley, Antarctica. Hughes Glacier is located towards the polar plateau on the western edge of the valley and flows from the southern Kukri Hills north into the valley. Canada and Commonwealth glaciers flow south into the valley from the Asgard range. Commonwealth glacier is located closest to the ocean on the east end of the valley. Canada glacier is located mid-valley, between Hughes and Commonwealth glaciers. Sediment was brought to the lab and incubated with added nutrient solutions. Solutions were then analyzed to determine change in nutrient concentration.Â
Data from: Plant trait response of tundra shrubs to permafrost and nutrient addition
<p>Plants may alter their strategies, such as growth and resource acquisition, as a result of climate change, especially in areas like the Arctic. These changes might affect in turn ecosystem functions and vegetation-climate interactions. Plant traits reflect both strategies and plant trade-offs in response to environmental conditions. In combination with observational data, experiments mimicking future climate conditions and data involving multiple leaf and stem traits, can contribute to a better mechanistic understanding of feedbacks between shrub growth strategies, permafrost thaw and carbon and energy fluxes.</p> <p>This dataset contains both metadata and plant trait data measured in individuals of four arctic shrub species under experimental conditions. The permafrost thaw and fertilization experiment (Peng et al., 2017) ran for four years (2011-2014) in the nature reserve of Kytalyk, north-eastern Siberia (70°49'N, 147°28'E). The shrub species, dominant at the research site, were the deciduous species <em>Betula nana</em> ssp. <em>exilis</em> (Sukazcev) Hultén and <em>Salix pulchra</em> Cham., and the evergreen species <em>Ledum palustre</em> ssp. <em>decumbens</em> (Aiton) Hultén and <em>Vaccinium vitis-idaea</em> L.</p>
Vertical profiles of leaf photosynthesis and leaf traits, and soil nutrients in two tropical rainforests in French Guiana before and after a three-year nitrogen and phosphorus addition experiment
<p>We provide a comprehensive dataset of vertical profiles of photosynthetic capacity and important leaf traits, including leaf N and P concentrations, from two three-year, large-scale fertilisation experiments conducted in two tropical rainforests in French Guiana. These data present a unique source of information to further improve model representations of the roles of N, P, and other leaf nutrients, in photosynthesis in tropical forests. To further facilitate the use of our data in syntheses and model studies, we provide an elaborate list of ancillary data, including important soil properties and nutrients, along with the leaf data. As environmental drivers are key to improve our understanding of carbon (C)-nutrient cycle interactions, this comprehensive dataset will aid to further enhance our understanding of how nutrient availability interacts with C uptake in tropical forests.</p>
Nutrient addition drives declines in grassland species richness primarily via enhanced species loss
<p><span>Declines in grassland diversity in response to nutrient addition are a general consequence of global change. This decline in species richness may be driven by multiple underlying processes operating at different timescales. Nutrient addition can reduce diversity by enhancing the rate of local extinction via competitive exclusion, or by reducing the rate of colonization by constraining the pool of species able to colonize under new conditions. Partitioning net change into extinction and colonization rates will better delineate the long-term effect of global change in grasslands. </span></p> <p><span>We synthesized changes in richness in response to experimental fertilization with nitrogen, phosphorus, and potassium with micronutrients across 30 grasslands. We quantified changes in local richness, colonization, and extinction over 8-10 years of nutrient addition, and compared these rates against control conditions to isolate the effect of nutrient addition from background dynamics. </span></p> <p><span>Total richness at steady state in the control plots was the sum of equal, relatively high rates of local colonization and extinction. On aggregate, 30-35% of initial species were lost and the same proportion of new species was gained at least once over a decade. Absolute turnover increased with site-level richness but was proportionately greater at lower-richness sites relative to starting richness. Loss of total richness with nutrient addition, especially N in combination with P or K, was driven by enhanced rates of extinction with a smaller contribution from reduced colonization. Enhanced extinction and reduced colonization were disproportionately among native species, perennials, and forbs. Reduced colonization plateaued after the first few (< 5) years after nutrient addition, while enhanced extinction continued throughout the first decade. </span></p> <p><span><strong>Synthesis</strong>:</span><span> Our results indicate a high rate of colonizations and extinctions underlying the richness of ambient communities, and that nutrient enhancement drives overall declines in diversity primarily by the exclusion of previously established species. Moreover, enhanced extinction continues over long time scales, suggesting continuous, long-term community responses and a need for long-term study to fully realize the extinction impact of increased nutrients on grassland composition. </span></p>
Fitness and niche differences are both important in explaining responses of plant diversity to nutrient addition
<p><span>Plant species loss due to eutrophication is a common phenomenon in temperate perennial grasslands. It occurs in a non-random fashion and is usually explained by increased competitive size asymmetry between co-occurring winner (tall species with optima in productive habitats) and loser species (small-statured plants typical for unproductive habitats). It remains unclear why nutrient addition decreases diversity in communities consisting of losers only, whereas it has little effect on winner-only communities. Here, I used the framework of modern coexistence theory to explore fertilization-driven changes in fitness and niche differences between different combinations of field-identified winner (W) and loser (L) species. I experimentally estimated competition parameters for plant species pairs constructed from a pool of eight species, including pairs of species from the same (WW, LL) and different species categories (LW) grown for approximately two years in control and fertilized conditions. Concurrently, I also followed plant species diversity in mesocosm communities constructed from the same species pool (four-species communities including winners, losers, or both) exposed to control and nutrient addition. </span><span>I found that nutrient addition can reduce but, unexpectedly, also promote species coexistence depending on the type of species pairs. Whereas nutrient addition eroded coexistence of losers with winners, but also with other losers, treatment had the opposite effect on the persistence of winner species. Fertilization induced large fitness differences between species in loser-winner and loser-loser combinations, but had little effect on the fitness differences of species within the winner-winner combination. In addition, the persistence of winner pairs was promoted by larger niche differences compared to loser species, irrespective of soil nutrients. The differences in how nutrient addition modified coexistence at the pairwise level were reflected by differences in evenness of multispecies communities assembled from the corresponding species categories.</span> <span>These results suggest that the effect of eutrophication on plant species richness cannot simply be explained by an increased competitive asymmetry. To fully understand the effect of fertilization on the diversity of temperate grasslands, interspecific and intraspecific interactions should be explored while considering differences in species' ecological optima.</span></p>
Dataset of ocean nutrient addition bioassay experiments
<p>Dataset of ocean nutrient addition bioassay experiments. Accompanies publication: 'Global analysis of ocean phytoplankton nutrient limitation reveals high prevalence of co-limitation' by Thomas J. Browning and C. Mark Moore.</p>
Nutrient addition drives declines in grassland species richness primarily via enhanced species loss
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A new method to reconstruct quantitative food webs and nutrient flows from isotope tracer addition experiments
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Data from: Plant cover changes drive plant and soil carbon pool responses in High Arctic dry heath exposed to decades of experimentally increased summer rain and nutrient addition
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Data from: Plant trait response of tundra shrubs to permafrost and nutrient addition
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Fitness and niche differences are both important in explaining responses of plant diversity to nutrient addition
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Shrunk coexistence: Cattle exclusion and nutrient addition intensify competition between native and exotic grasses with low phenological overlap
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Data from: Long-term nutrient addition and grazing exclusion determine flower abundance, diversity and community composition in high-latitude grasslands
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Long-term low-level nutrient additions significantly impact a low arctic mesic tundra plant community, but species responses differ from high-level fertilization: Implications for predicting climate warming impacts
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Data from: Phytoplankton growth and stoichiometric responses to warming, nutrient addition and grazing depend on lake productivity and cell size
<p>Global change involves shifts in multiple environmental factors that act in concert to shape ecological systems in ways that depend on local biotic and abiotic conditions. Little is known about the effects of combined global change stressors on phytoplankton communities, and particularly how these are mediated by distinct community properties such as productivity, grazing pressure and size distribution. Here, we tested for the effects of warming and eutrophication on phytoplankton net growth rate and C:N:P stoichiometry in two phytoplankton cell size fractions (<30 μm and >30 μm) in the presence and absence of grazing in microcosm experiments. Because effects may also depend on lake productivity, we used phytoplankton communities from three Dutch lakes spanning a trophic gradient. We measured the response of each community to multifactorial combinations of temperature, nutrient, and grazing treatments and found that nutrients elevated net growth rates and reduced carbon:nutrient ratios of all three phytoplankton communities. Warming effects on growth and stoichiometry depended on nutrient supply and lake productivity, with enhanced growth in the most productive community dominated by cyanobacteria, and strongest stoichiometric responses in the most oligotrophic community at ambient nutrient levels. Grazing effects were also most evident in the most oligotrophic community, with reduced net growth rates and phytoplankton C:P stoichiometry that suggests consumer‐driven nutrient recycling. Our experiments indicate that stoichiometric responses to warming and interactions with nutrient addition and grazing are not universal but depend on lake productivity and cell size distribution.</p>
Mowing does not redress the negative effect of nutrient addition on alpha and beta diversity in a temperate grassland
<p>Species loss due to an increasing number of added nutrients has been explained by both light competition through biomass increase and by niche dimension reduction as a result of species specific limiting soil resources trade-offs. Disturbances, by reducing community biomass, species dominance and increasing light availability, may counteract above ground nutrient effects. However, it is unknown if diversity loss at local or spatial scales generated by increasing number of added nutrients can be redressed with canopy disturbance.</p> <p>We evaluated if local (alpha) and spatial scale (beta) diversity loss generated by the number of added nutrients can be reverted by disturbances in Flooding Pampa grasslands, Argentina. In a 4-yr replicated field experiment, we added soil resources combining nitrogen, phosphorus and potassium to obtain 0, 1, 2 or 3 nutrients and manipulated the regime of canopy disturbance by seasonal mowing and biomass removal.</p> <p>We found that the increasing number of added nutrients strongly reduced local and spatial plant diversity, despite biomass and light changes generated by mowing. In mown plots, nutrient driven local diversity loss was intensified along time, thus increasing species dominance. While mowing did not affect dominant species loss, increasing number of added nutrients promoted rare species loss and reduced spatial dissimilarity. Furthermore, mowing increased local and spatial diversity regardless light or biomass effects, suggesting alternative pathway effects for disturbance.</p> <p>Synthesis: Our results demonstrated that even when disturbance generated a positive effect on local and spatial diversity, it did not completely counteract the negative effect of number of added nutrients. Thus, the relative importance of above and belowground resource competition may change when chronic disturbances alter community dominance. Under low light availability, above-ground competition may drive species richness loss but when disturbance reduces light limitation, the increasing number of added nutrients may reduce niche dimensionality and thus species coexistence. In sum, faced with the need to manage eutrophized grasslands, our study showed that disturbance may not completely mitigate the negative effect of multiple nutrient inputs on local and spatial grassland diversi</p>
Data from: Simulated caribou browsing limits the effect of nutrient addition on the growth of Betula glandulosa, an expanding shrub species in Eastern Canada
1.Warmer summer temperatures and enhanced soil fertility increase shrub growth in tundra ecosystems, and these factors have likely contributed to shrub expansion at the circumpolar scale over the last decades. Conversely, large herbivores have the potential to counteract the positive impacts of climate change on shrub growth. Indeed, by stripping the leaves, herbivores have the potential to control the growth of shrub species and, consequently, limit their expansion. 2.To disentangle the impacts of climate change and herbivory on Betula glandulosa Michx., we conducted a 5-yr factorial experiment near Deception Bay, Nunavik, Canada, in which we simulated warmer temperatures, increased nitrogen availability and three caribou browsing intensities during the growing season. At the end of the experiment, we harvested the aboveground biomass of B. glandulosa and conducted dendrochronological analyses on stems. 3.Fertilized plots under ambient temperature had 34% greater shrub biomass than plots assigned to the combined treatment of nitrogen addition and warmer temperatures. Browsing intensity had no effect on final biomass. Nitrogen addition increased radial growth (18-33%; 3 years out of 5). Overall, browsing had a cumulative negative impact on B. glandulosa radial growth during the 5-yr experiment. While browsing had no effect in the first year of the experiment, moderate browsing (leaves stripped on 25% of available shoots) decreased radial growth by 27% at year 2, 32% at year 4 and 27% at year 5. Heavy browsing (leaves stripped on 75% of available shoots annually) decreased radial growth by approximately 27% at year 2, 37% at year 3, 50% at year 4 and 48% at year 5. We did not observe significant interactions between browsing, temperature and nitrogen availability. 4.Synthesis. Our results clearly showed that caribou browsing may limit the growth of B. glandulosa, and thus can potentially limit its expansion. Herbivory should thus be considered when predicting tundra vegetation changes in the Arctic, at least in areas with high herbivore densities.
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Allen Brain Atlas
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OpenNeuro
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