ALBERT

Description: Climate change and human activities have caused a shift in vegetation composition and soil biogeochemical cycles of alpine wetlands on the Tibetan Plateau. The primary goal of this study was to test for associations between community-weighted mean (CWM) traits, functional diversity, and soil properties during wetland drying. We collected soil samples and investigated the aboveground vegetation in swamp, swamp meadow, and typical meadow environments. Four CWM trait values (specific leaf area is SLA, leaf dry matter content is LDMC, leaf area is LA, and mature plant height is MPH) for 42 common species were measured across the three habitats; three components of functional diversity (functional richness, functional evenness, and functional divergence) were also quantified at these sites. Our results showed that the drying of the wetland dramatically altered plant community and soil properties. There was a significant correlation between CWM of traits and soil properties, but not a significant correlation between functional diversity and soil properties. Our results further showed that CWM-LA, CWM-SLA, and CWM-LDMC had positive correlations with soil readily available nutrients (available nitrogen, AN; available phosphorus, AP), but negative correlations with total soil nutrients (soil organic carbon is SOC, total nitrogen is TN, and total phosphorus is TP). Our study demonstrated that simple, quantitative plant functional traits, but not functional diversity, are directly related to soil C and N properties, and they likely play an important role in plant–soil interactions. Our results also suggest that functional identity of species may be more important than functional diversity in influencing ecosystem processes during wetland drying.

Description: Soils in Arctic and boreal ecosystems store twice as much carbon as the atmosphere, a portion of which may be released as high-latitude soils warm. Some of the uncertainty in the timing and magnitude of the permafrost–climate feedback stems from complex interactions between ecosystem properties and soil thermal dynamics. Terrestrial ecosystems fundamentally regulate the response of permafrost to climate change by influencing surface energy partitioning and the thermal properties of soil itself. Here we review how Arctic and boreal ecosystem processes influence thermal dynamics in permafrost soil and how these linkages may evolve in response to climate change. While many of the ecosystem characteristics and processes affecting soil thermal dynamics have been examined individually (e.g., vegetation, soil moisture, and soil structure), interactions among these processes are less understood. Changes in ecosystem type and vegetation characteristics will alter spatial patterns of interactions between climate and permafrost. In addition to shrub expansion, other vegetation responses to changes in climate and rapidly changing disturbance regimes will affect ecosystem surface energy partitioning in ways that are important for permafrost. Lastly, changes in vegetation and ecosystem distribution will lead to regional and global biophysical and biogeochemical climate feedbacks that may compound or offset local impacts on permafrost soils. Consequently, accurate prediction of the permafrost carbon climate feedback will require detailed understanding of changes in terrestrial ecosystem distribution and function, which depend on the net effects of multiple feedback processes operating across scales in space and time.

Description: Photochemical reactions represent the main pathway for the removal of non-methane volatile organic compounds (VOCs) in the atmosphere. VOCs may react with hydroxyl radical (OH), the most important atmospheric oxidant, or they can be photolyzed by actinic radiation. In the presence of clouds and fog, VOCs may partition into the aqueous phase where they can undergo aqueous photolysis and/or reaction with dissolved OH. The significance of direct aqueous photolysis is largely uncertain due to the lack of published absorption cross sections and photolysis quantum yields. In light of this, we strive to identify atmospherically relevant VOCs where removal by aqueous photolysis may be a significant sink. The relative importance of different photochemical sinks is assessed by calculating the ratios of the removal rates inside air parcels containing cloud and fog droplets. This relative approach provides useful information in spite of the limited aqueous photolysis data. Results of this work should help guide researchers in identifying molecules that are the most likely to undergo aqueous OH oxidation and photolysis. For example, we find that out of the 27 atmospherically relevant species investigated, the removal of glyceraldehyde and pyruvic acid by aqueous photolysis is potentially an important sink. We also determine the relative magnitudes of these four chemical sinks for the set of relevant organic compounds.

Description: We develop the thermodynamic underpinnings of a two-dimensional volatility basis set (2D-VBS) employing saturation mass concentration (Co) and the oxygen content (O:C) to describe volatility, mixing thermodynamics, and chemical evolution of organic aerosol. The work addresses a simple question: "Can we reasonably constrain organic-aerosol composition in the atmosphere based on only two measurable organic properties, volatility and the extent of oxygenation?" This is an extension of our earlier one-dimensional approach employing volatility only (C* = γ Co, where γ is an activity coefficient). Using available constraints on bulk organic-aerosol composition, we argue that one can reasonably predict the composition of organics (carbon, oxygen and hydrogen numbers) given a location in the Co – O:C space. Further, we argue that we can constrain the activity coefficients at various locations in this space based on the O:C of the organic aerosol.

Description: Gas-phase photolysis is an important tropospheric sink for many carbonyl compounds; however the significance of direct photolysis of these compounds dissolved in cloud and fog droplets is uncertain. We develop a theoretical approach to assess the importance of aqueous photolysis for a series of carbonyls that possess carboxyl and hydroxyl functional groups by comparison with rates of other atmospheric processes. We use computationally and experimentally derived effective Henry's law constants, hydration equilibrium parameters, aqueous hydroxyl radical (OH) rate constants, and optical extinction coefficients to identify types of compounds that will (or will not) have competitive aqueous photolysis rates. We also present molecular dynamics simulations designed to estimate gas- and aqueous-phase extinction coefficients of unstudied atmospherically relevant compounds found in d-limonene and isoprene secondary organic aerosol. In addition, experiments designed to measure the photolysis rate of glyceraldehyde, an atmospherically relevant water-soluble organic compound, reveal that aqueous quantum yields are highly molecule-specific and cannot be extrapolated from measurements of structurally similar compounds. We find that only two out of the 92 carbonyl compounds investigated, pyruvic acid and acetoacetic acid, may have aqueous photolysis rates that exceed the rate of oxidation by dissolved OH. For almost all carbonyl compounds lacking α,β-conjugation that were investigated, atmospheric removal by direct photolysis in cloud and fog droplets can be neglected under typical atmospheric conditions.

Description: Photochemical reactions represent the main pathway for the removal of non-methane volatile organic compounds (VOCs) in the atmosphere. VOCs may react with hydroxyl radical (OH), the most important atmospheric oxidant, or they can be photolyzed by actinic radiation. In the presence of clouds and fog, VOCs may partition into the aqueous phase where they can undergo aqueous photolysis and/or reaction with dissolved OH. The significance of direct aqueous photolysis is largely uncertain due to the lack of published absorption cross sections and photolysis quantum yields. In light of this, we strive to identify atmospherically relevant VOCs where removal by aqueous photolysis may be a significant sink. The relative importance of different photochemical sinks is assessed by calculating the ratios of the removal rates inside air parcels containing cloud and fog droplets. This relative approach provides useful information in spite of the limited aqueous photolysis data. Results of this work should help guide researchers in identifying molecules that are the most likely to undergo aqueous OH oxidation and photolysis. We find that out of the 27 atmospherically relevant species investigated, the removal of glyceraldehyde and pyruvic acid by aqueous photolysis is potentially an important sink. We also determine the relative magnitudes of these four chemical sinks for the set of relevant organic compounds.

Description: In topographically complex watersheds, landscape position and vegetation heterogeneity can alter the soil water regime through both lateral and vertical redistribution, respectively. These alterations of soil moisture may have significant impacts on the spatial heterogeneity of biogeochemical cycles throughout the watershed. To evaluate how landscape position and vegetation heterogeneity affect soil CO2 efflux (FSOIL) we conducted observations across the Weimer Run watershed (373 ha), located near Davis, West Virginia, for three growing seasons with varying precipitation (2010 – 1042 mm; 2011 – 1739 mm; 2012 – 1244 mm; precipitation data from BDKW2 station, MesoWest, University of Utah). An apparent soil temperature threshold of 11 °C at 12 cm depth on FSOIL was observed in our data – where FSOIL rates greatly increase in variance above this threshold. For analysis, FSOIL values above this threshold were isolated and examined. Differences in FSOIL among years were apparent by elevation (F4,633 = 3.17; p = 0.013) and by vegetation cover (F4, 633 = 2.96; p = 0.019). For the Weimer Run watershed, vegetation exerts the major control on soil CO2 efflux (FSOIL), with the plots beneath shrubs at all elevations for all years showing the greatest mean rates of FSOIL (6.07 μmol CO2 m-2 s-1) compared to plots beneath closed-forest canopy (4.69 μmol CO2 m-2 s-1) and plots located in open, forest gaps (4.09 μmol CO2 m-2 s-1) plots. During periods of high soil moisture, we find that CO2 efflux rates are constrained and that maximum efflux rates in this system occur during periods of average to below average soil water availability. These findings offer valuable insight into the processes occurring within these topographically complex, temperate and humid systems, and the interactions of abiotic and biotic factors mediating biogeochemical cycles. With possible changing rainfall patterns as predicted by climate models, it is important to understand the couplings between water and carbon cycling at the watershed and landscape scales, and their potential dynamics under global change scenarios.

Description: Gas phase photolysis is an important tropospheric sink for many carbonyl compounds, however the significance of direct photolysis of carbonyl compounds dissolved in cloud and fog droplets is uncertain. We develop a theoretical approach to assess the importance of aqueous photolysis for a series of carbonyls that possess carboxyl and hydroxyl functional groups by comparison with rates of other atmospheric processes. We use computationally and experimentally derived Henry's law parameters, hydration equilibrium parameters, aqueous hydroxyl radical (OH) rate constants, and optical extinction coefficients to identify types of compounds that will not have competitive aqueous photolysis rates. We also present molecular dynamics simulations of atmospherically relevant carbonyl compounds designed to estimate gas and aqueous phase extinction coefficients. In addition, experiments designed to measure the photolysis rate of glyceraldehyde, an atmospherically relevant water soluble organic compound, reveal that aqueous quantum yields are highly molecule-specific and cannot be extrapolated from measurements of structurally similar compounds. We find that only three out of the 92 carbonyl compounds investigated, pyruvic acid, 3-oxobutanoic acid, and 3-oxopropanoic acid, may have aqueous photolysis rates that exceed the rate of oxidation by dissolved OH. For almost all carbonyl compounds lacking α, β conjugation, atmospheric removal by direct photolysis in cloud and fog droplets can be neglected.

Description: In topographically complex watersheds, landscape position and vegetation heterogeneity can alter the soil water regime through both lateral and vertical redistribution, respectively. These alterations of soil moisture may have significant impacts on the spatial heterogeneity of biogeochemical cycles throughout the watershed. To evaluate how landscape position and vegetation heterogeneity affect soil CO2 efflux (FSOIL), we conducted observations across the Weimer Run watershed (373 ha), located near Davis, West Virginia, for three growing seasons with varying precipitation. An apparent soil temperature threshold of 11 °C for FSOIL at 12 cm depth was observed in our data, where FSOIL rates greatly increase in variance above this threshold. We therefore focus our analyses of FSOIL on instances in which soil temperature values were above this threshold. Vegetation had the greatest effect on FSOIL rates, with plots beneath shrubs at all elevations, for all years, showing the greatest mean rates of FSOIL (6.07 μmol CO2 m−2 s−1) compared to plots beneath closed-forest canopy (4.69 μmol CO2 m−2 s−1) and plots located in open, forest gap (4.09 μmol CO2 m−2 s−1) plots. During periods of high soil moisture, we find that CO2 efflux rates are constrained, and that maximum efflux rates occur during periods of average to below-average soil water availability. While vegetation was the variable most related to FSOIL, there is also strong interannual variability in fluxes determined by the interaction of annual precipitation and topography. These findings add to the current theoretical constructs related to the interactions of moisture and vegetation in biogeochemical cycles within topographically complex watersheds.

Description: We develop the thermodynamic underpinnings of a two-dimensional volatility basis set (2-D-VBS) employing saturation concentration (Co) and the oxygen content (O:C) to describe volatility, mixing thermodynamics, and chemical evolution of organic aerosol. This is an extension of our earlier one-dimensional approach employing C* only (C*=γ Co, where γ is an activity coefficient). We apply a mean-field approximation for organic aerosol, describing interactions of carbon and oxygen groups in individual molecules (solutes) with carbon and oxygen groups in the organic-aerosol solvent. In so doing, we show that a linear structure activity relation (SAR) describing the single-component Co of a molecule is directly tied to ideal solution (Raoult's Law) behavior. Conversely, non-ideal solution behavior (activity coefficients) and a slightly non-linear SAR emerge from off-diagonal (carbon-oxygen) interaction elements. From this foundation we can build a self-consistent description of OA mixing thermodynamics, including predicted saturation concentrations and activity coefficients (and phase separation) for various solutions from just four free parameters: the carbon number of a hydrocarbon with a 1 μg m−3 Co, and the carbon-carbon, oxygen-oxygen, and non-ideal carbon-oxygen terms. This treatment establishes the mean molecular formula for organics within this 2-D space as well as activity coefficients for molecules within this space interacting with any bulk OA phase described by an average O:C.