94 research outputs found
Increasing Ca2+ Deposition in the Western US: The Role of Mineral Aerosols
Considerable research has focused on the role of industrial emissions in controlling the acidity of precipitation; however, much less research has focused on the role of mineral aerosols emitted from soils. According to data published by the National Atmospheric Deposition Network (NADP), over the past 17 years Ca2+ deposition has increased over large regions of the US. A trend analysis to determine regions of significant change in Ca2+ deposition revealed statistically significant increases in three broad regions within the western half of the country: the inter-mountain west, the midwest, and the northwest. We evaluated potential changes in sources of calcium to the atmosphere including soil erosion, industrial emissions, forest fires, and sea-salt aerosols to determine the cause of rising atmospheric calcium deposition. Based on our evaluation, the most parsimonious explanation for increased Ca2+ deposition is an increase in mineral aerosol emissions from within the western US. This explanation is corroborated by independent evidence showing increases in the frequency of dust storms and low-visibility days across regions of the western US. Furthermore, our analysis indicates that the increase in mineral aerosol emissions is most likely due to (1) increased aridity and wind transport and (2) increased area and intensity of upwind human activities. Changes in atmospheric dust concentrations can have important ecological implications through the contribution of acid neutralizing capacity to both precipitation and regions of deposition. Thus increased dust emissions have the potential to ameliorate the detrimental effects of acid precipitation on terrestrial ecosystems, though dust may exacerbate the impacts of air quality on human health
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Variation in Soil Carbon Dioxide Efflux at Two Spatial Scales in a Topographically Complex Boreal Forest
Carbon dynamics of high latitude regions are an important and highly uncertain component of global carbon budgets, and efforts to constrain estimates of soil-atmosphere carbon exchange in these regions are contingent on accurate representations of spatial and temporal variability in carbon fluxes. This study explores spatial and temporal variability in soil-atmosphere carbon dynamics at both fine and coarse spatial scales in a high-elevation, permafrost-dominated boreal black spruce forest. We evaluate the importance of landscape level investigations of soil-atmosphere carbon dynamics by characterizing seasonal trends in soil-atmosphere carbon exchange, describing soil temperature-moisture-respiration relations, and quantifying temporal and spatial variability at two spatial scales: the plot scale (0-5m) and the landscape scale (500-1000m). Plot-scale spatial variability (average variation on a given measurement day) in soil CO2 efflux ranged from a coefficient of variation (CV) 0.25 to 0.69, and plot-scale temporal variability (average variation of plots across measurement days) in efflux ranged from a CV of 0.19 to 0.36. Landscape-scale spatial and temporal variability in efflux was represented by a CV of 0.40 and 0.31 respectively, indicating that plot-scale spatial variability in soil respiration is as great as landscape-scale spatial variability at this site. While soil respiration was related to soil temperature at both the plot and landscape-scale, landscape level descriptions of soil moisture were necessary to define soil respiration-moisture relations. Soil moisture variability was also integral to explaining temporal variability in soil respiration. Our results have important implications for research efforts in high latitude regions where remote study sites make landscape-scale field campaigns challenging
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Short and long-term carbon balance of bioenergy electricity production fueled by forest treatments
Background:
Forests store large amounts of carbon in forest biomass, and this carbon can be released to the atmosphere following forest disturbance or management. In the western US, forest fuel reduction treatments designed to reduce the risk of high severity wildfire can change forest carbon balance by removing carbon in the form of biomass, and by altering future potential wildfire behavior in the treated stand. Forest treatment carbon balance is further affected by the fate of this biomass removed from the forest, and the occurrence and intensity of a future wildfire in this stand. In this study we investigate the carbon balance of a forest treatment with varying fates of harvested biomass, including use for bioenergy electricity production, and under varying scenarios of future disturbance and regeneration.
Results:
Bioenergy is a carbon intensive energy source; in our study we find that carbon emissions from bioenergy electricity production are nearly twice that of coal for the same amount of electricity. However, some emissions from bioenergy electricity production are offset by avoided fossil fuel electricity emissions. The carbon benefit achieved by using harvested biomass for bioenergy electricity production may be increased through avoided pyrogenic emissions if the forest treatment can effectively reduce severity.
Conclusion:
Forest treatments with the use of harvested biomass for electricity generation can reduce carbon emissions to the atmosphere by offsetting fossil fuel electricity generation emissions, and potentially by avoided pyrogenic emissions due to reduced intensity and severity of a future wildfire in the treated stand. However, changes in future wildfire and regeneration regimes may affect forest carbon balance and these climate-induced changes may influence forest carbon balance as much, or more, than bioenergy production
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Evidence for Accelerated Weathering and Sulfate Export in High Alpine Environments
High elevation alpine ecosystems—the \u27water towers of the world\u27—provide water for human populations around the globe. Active geomorphic features such as glaciers and permafrost leave alpine ecosystems susceptible to changes in climate which could also lead to changing biogeochemistry and water quality. Here, we synthesize recent changes in high-elevation stream chemistry from multiple sites that demonstrate a consistent and widespread pattern of increasing sulfate and base cation concentrations or fluxes. This trend has occurred over the past 30 years and is consistent across multiple sites in the Rocky Mountains of the United States, western Canada, the European Alps, the Icelandic Shield, and the Himalayas in Asia. To better understand these recent changes and to examine the potential causes of increased sulfur and base cation concentrations in surface waters, we present a synthesis of global records as well as a high resolution 33 year record of atmospheric deposition and river export data from a long-term ecological research site in Colorado, USA. We evaluate which factors may be driving global shifts in stream chemistry including atmospheric deposition trends and broad climatic patterns. Our analysis suggests that recent changes in climate may be stimulating changes to hydrology and/or geomorphic processes, which in turn lead to accelerated weathering of bedrock. This cascade of effects has broad implications for the chemistry and quality of important surface water resources
Separating the Influences of Diagenesis, Productivity and Anthropogenic Nitrogen Deposition on Sedimentary δ15N Variations
The stable isotopic composition of nitrogen (δ15N) in organic lake sediments is frequently used to infer changes in the source or cycling of N prior to sedimentation. However, diagenetic processes that occur after sedimentation can systematically alter the primary isotopic signal recorded in sedimentary organic matter and must be accounted for in order to detect changes in the δ15N of nitrogen inputs to the sediment surface. Here we present a null model that estimates the diagenetic effect on sedimentary lake δ15N records. The model was tested using lake sediment cores from relatively pristine alpine lakes in the Wind River and Teton Ranges of Wyoming, USA. Model-inferred increases in productivity were tested against independent productivity proxies (diatom accumulation rates and the planktonic to benthic ratio), and inferred changes in anthropogenic nitrogen contribution were validated with records of atmospheric nitrogen deposition from the nearby Fremont Glacier, Wyoming. Diagenetic overprinting significantly altered sediment δ15N profiles, and the degree of alteration was not constant through time. Of the cores analyzed, ∼30–70% of the variability can be explained by diagenesis alone, with the remainder explained by either a change in productivity or a change in the isotopic composition of the source material. Our null model of isotopic fractionation proved to be successful at separating the diagenetic overprinting from other causes of isotopic shifts, thereby providing environmental scientists with an analytical tool to partition the effects of diagenesis and environmental change on sedimentary δ15N values
Dust Mediated Transfer of Phosphorus to Alpine Lake Ecosystems of the Wind River Range, Wyoming, USA
Alpine lakes receive a large fraction of their nutrients from atmospheric sources and are consequently sensitive to variations in both the amount and chemistry of atmospheric deposition. In this study we explored the spatial changes in lake water chemistry and biology along a gradient of dust deposition in the Wind River Range, Wyoming. Regional differences were explored using the variation in bulk deposition, lake water, sediment, and bedrock geochemistry and catchment characteristics. Dust deposition rates in the Southwestern region averaged 3.34 g m−2 year−1, approximately three times higher than deposition rates in the Northwestern region (average 1.06 g m−2 year−1). Dust-P deposition rates ranged from 87 µg P m2 day−1 in the Northwestern region to 276 µg P m2 day−1 in the Southwestern region. Subalpine and alpine lakes in the Southwestern region had greater total phosphorus (TP) concentrations (5–13 µg L−1) and greater sediment phosphorus (SP) concentrations (2–5 mg g−1) than similar lakes elsewhere in the region (1–8 µg L−1 TP, 0.5–2 mg g−1 SP). Lake phosphorus concentrations were related to dissolved organic carbon (DOC) across vegetation gradients, but related to the percent of bare rock, catchment area to lake area, and catchment steepness across dust deposition gradients. Modern phytoplankton and zooplankton biomasses were two orders of magnitude greater in the Southwest than in the Northwest, and alpine lakes in the Southwest had a unique diatom species assemblage with relatively higher concentrations of Asterionella formosa, Pseudostaurosira pseudoconstruens, and Pseudostaurosira brevistriata. These results suggests that catchment controls on P export to lakes (i.e. DOC) are overridden in dominantly bare rock basins where poor soils cannot effectively retain dust deposited P
Short and long-term carbon balance of bioenergy electricity production fueled by forest treatments
Abstract Background: Forests store large amounts of carbon in forest biomass, and this carbon can be released to the atmosphere following forest disturbance or management. In the western US, forest fuel reduction treatments designed to reduce the risk of high severity wildfire can change forest carbon balance by removing carbon in the form of biomass, and by altering future potential wildfire behavior in the treated stand. Forest treatment carbon balance is further affected by the fate of this biomass removed from the forest, and the occurrence and intensity of a future wildfire in this stand. In this study we investigate the carbon balance of a forest treatment with varying fates of harvested biomass, including use for bioenergy electricity production, and under varying scenarios of future disturbance and regeneration
Is Atmospheric Phosphorus Pollution Altering Global Alpine Lake Stoichiometry?
Anthropogenic activities have significantly altered atmospheric chemistry and changed the global mobility of key macronutrients. Here we show that contemporary global patterns in nitrogen (N) and phosphorus (P) emissions drive large hemispheric variation in precipitation chemistry. These global patterns of nutrient emission and deposition (N:P) are in turn closely reflected in the water chemistry of naturally oligotrophic lakes (r2 = 0.81, p \u3c 0.0001). Observed increases in anthropogenic N deposition play a role in nutrient concentrations (r2 = 0.20, p \u3c 0.05); however, atmospheric deposition of P appears to be major contributor to this pattern (r2 = 0.65, p \u3c 0.0001). Atmospheric simulations indicate a global increase in P deposition by 1.4 times the preindustrial rate largely due to increased dust and biomass burning emissions. Although changes in the mass flux of global P deposition are smaller than for N, the impacts on primary productivity may be greater because, on average, one unit of increased P deposition has 16 times the influence of one unit of N deposition. These stoichiometric considerations, combined with the evidence presented here, suggest that increases in P deposition may be a major driver of alpine Lake trophic status, particularly in the Southern Hemisphere. These results underscore the need for the broader scientific community to consider the impact of atmospheric phosphorus deposition on the water quality of naturally oligotrophic lakes
IR and UV Galaxies at z=0.6 -- Evolution of Dust Attenuation and Stellar Mass as Revealed by SWIRE and GALEX
We study dust attenuation and stellar mass of star-forming
galaxies using new SWIRE observations in IR and GALEX observations in UV. Two
samples are selected from the SWIRE and GALEX source catalogs in the
SWIRE/GALEX field ELAIS-N1-00 ( deg). The UV selected sample
has 600 galaxies with photometric redshift (hereafter photo-z) and NUV (corresponding to \rm L_{FUV} \geq 10^{9.6} L_\sun).
The IR selected sample contains 430 galaxies with mJy
(\rm L_{dust} \geq 10^{10.8} L_\sun) in the same photo-z range. It is found
that the mean ratios of the z=0.6 UV galaxies are
consistent with that of their z=0 counterparts of the same . For
IR galaxies, the mean ratios of the z=0.6 LIRGs (\rm
L_{dust} \sim 10^{11} L_\sun) are about a factor of 2 lower than local LIRGs,
whereas z=0.6 ULIRGs (\rm L_{dust} \sim 10^{12} L_\sun) have the same mean
ratios as their local counterparts. This is consistent
with the hypothesis that the dominant component of LIRG population has changed
from large, gas rich spirals at z to major-mergers at z=0. The stellar
mass of z=0.6 UV galaxies of \rm L_{FUV} \leq 10^{10.2} L_\sun is about a
factor 2 less than their local counterparts of the same luminosity, indicating
growth of these galaxies. The mass of z=0.6 UV lunmous galaxies (UVLGs: \rm
L_{FUV} > 10^{10.2} L_\sun) and IR selected galaxies, which are nearly
exclusively LIRGs and ULIRGs, is the same as their local counterparts.Comment: 27 pages, 8 figures, to be published in the Astrophysical Journal
Supplement series dedicated to GALEX result
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