Allen H. Goldstein

FLUXNET: A New Tool to Study the Temporal and Spatial Variability of Ecosystem-Scale Carbon Dioxide, Water Vapor, and Energy Flux Densities

FLUXNET is a global network of micrometeorological flux measurement sites that measure the exchanges of carbon dioxide, water vapor, and energy between the biosphere and atmosphere. At present over 140 sites are operating on a long-term and continuous basis. Vegetation under study includes temperate conifer and broadleaved (deciduous and evergreen) forests, tropical and boreal forests, crops, grasslands, chaparral, wetlands, and tundra. Sites exist on five continents and their latitudinal distribution ranges from 70°N to 30°S. FLUXNET has several primary functions. First, it provides infrastructure for compiling, archiving, and distributing carbon, water, and energy flux measurement, and meteorological, plant, and soil data to the science community. (Data and site information are available online at the FLUXNET Web site, http://www-eosdis.ornl.gov/FLUXNET/.) Second, the project supports calibration and flux intercomparison activities. This activity ensures that data from the regional networks are intercomparable. And third, FLUXNET supports the synthesis, discussion, and communication of ideas and data by supporting project scientists, workshops, and visiting scientists. The overarching goal is to provide information for validating computations of net primary productivity, evaporation, and energy absorption that are being generated by sensors mounted on the NASA Terra satellite. Data being compiled by FLUXNET are being used to quantify and compare magnitudes and dynamics of annual ecosystem carbon and water balances, to quantify the response of stand-scale carbon dioxide and water vapor flux densities to controlling biotic and abiotic factors, and to validate a hierarchy of soil–plant–atmosphere trace gas exchange models. Findings so far include 1) net CO 2 exchange of temperate broadleaved forests increases by about 5.7 g C m −2 day −1 for each additional day that the growing season is extended; 2) the sensitivity of net ecosystem CO 2 exchange to sunlight doubles if the sky is cloudy rather than clear; 3) the spectrum of CO 2 flux density exhibits peaks at timescales of days, weeks, and years, and a spectral gap exists at the month timescale; 4) the optimal temperature of net CO 2 exchange varies with mean summer temperature; and 5) stand age affects carbon dioxide and water vapor flux densities.

Energy balance closure at FLUXNET sites

A comprehensive evaluation of energy balance closure is performed across 22 sites and 50 site-years in FLUXNET, a network of eddy covariance sites measuring long-term carbon and energy fluxes in contrasting ecosystems and climates. Energy balance closure was evaluated by statistical regression of turbulent energy fluxes (sensible and latent heat (LE)) against available energy (net radiation, less the energy stored) and by solving for the energy balance ratio, the ratio of turbulent energy fluxes to available energy. These methods indicate a general lack of closure at most sites, with a mean imbalance in the order of 20%. The imbalance was prevalent in all measured vegetation types and in climates ranging from Mediterranean to temperate and arctic. There were no clear differences between sites using open and closed path infrared gas analyzers. At a majority of sites closure improved with turbulent intensity (friction velocity), but lack of total closure was still prevalent under most conditions. The imbalance was greatest during nocturnal periods. The results suggest that estimates of the scalar turbulent fluxes of sensible and LE are underestimated and/or that available energy is overestimated. The implications on interpreting long-term CO2 fluxes at FLUXNET sites depends on whether the imbalance results primarily from general errors associated

Modeling and measuring the effects of disturbance history and climate on carbon and water budgets in evergreen needleleaf forests

The effects of disturbance history, climate, and changes in atmospheric carbon dioxide (CO2) concentration and nitrogen deposition (Ndep) on carbon and water fluxes in seven North American evergreen forests are assessed using a coupled water–carbon–nitrogen model, canopy-scale flux observations, and descriptions of the vegetation type, management practices, and disturbance histories at each site. The effects of interannual climate variability, disturbance history, and vegetation ecophysiology on carbon and water fluxes and storage are integrated by the ecosystem process model Biome-BGC, with results compared to site biometric analyses and eddy covariance observations aggregated by month and year. Model results suggest that variation between sites in net ecosystem carbon exchange (NEE) is largely a function of disturbance history, with important secondary effects from site climate, vegetation ecophysiology, and changing atmospheric CO2 and Ndep. The timing and magnitude of fluxes following disturbance depend on disturbance type and intensity, and on post-harvest management treatments such as burning, fertilization and replanting. The modeled effects of increasing atmospheric CO 2 on NEE are generally limited by N availability, but are greatly increased following disturbance due to increased N mineralization and reduced plant N demand. Modeled rates of carbon sequestration over the past 200 years are driven by the rate of change in CO2 concentration for old sites experiencing low rates of N dep. The model produced good estimates of between-site variation in leaf area index, with mixed performance for between- and within-site variation in evapotranspiration. There is a model bias

Ecosystem carbon dioxide fluxes after disturbance in forests of North America

Disturbances are important for renewal of North American forests. Here we summarize more than 180 site years of eddy covariance measurements of carbon dioxide flux made at forest chronosequences in North America. The disturbances included stand-replacing fire (Alaska, Arizona, Manitoba, and Saskatchewan) and harvest (British Columbia, Florida, New Brunswick, Oregon, Quebec, Saskatchewan, and Wisconsin) events, insect infestations (gypsy moth, forest tent caterpillar, and mountain pine beetle), Hurricane Wilma, and silvicultural thinning (Arizona, California, and New Brunswick). Net ecosystem production (NEP) showed a carbon loss from all ecosystems following a stand-replacing disturbance, becoming a carbon sink by 20 years for all ecosystems and by 10 years for most. Maximum carbon losses following disturbance (g C m−2y−1) ranged from 1270 in Florida to 200 in boreal ecosystems. Similarly, for forests less than 100 years old, maximum uptake (g C m−2y−1) was 1180 in Florida mangroves and 210 in boreal ecosystems. More temperate forests had intermediate fluxes. Boreal ecosystems were relatively time invariant after 20 years, whereas western ecosystems tended to increase in carbon gain over time. This was driven mostly by gross photosynthetic production (GPP) because total ecosystem respiration (ER) and heterotrophic respiration were relatively invariant with age. GPP/ER was as low as 0.2 immediately following stand-replacing disturbance reaching a constant value of 1.2 after 20 years. NEP following insect defoliations and silvicultural thinning showed lesser changes than stand-replacing events, with decreases in the year of disturbance followed by rapid recovery. NEP decreased in a mangrove ecosystem following Hurricane Wilma because of a decrease in GPP and an increase in ER.

Effects of climate variability on the carbon dioxide, water, and sensible heat fluxes above a ponderosa pine plantation in the Sierra Nevada (CA)

Fluxes of CO2, water vapor, and sensible heat were measured by the eddy covariance method above a young ponderosa pine plantation in the Sierra Nevada Mountains (CA) over two growing seasons (1 June‐10 September 1997 and 1 May‐30 October 1998). The Mediterranean-type climate of California is characterized by a protracted summer drought, with precipitation occurring mainly from October through May. While drought stress increased continuously over both summer growing seasons, 1998 was wetter and cooler than average due to El Nino climate patterns and 1997 was hotter and drier than average. One extreme 3-day heat wave in 1997 (Days 218‐221) caused a step change in the relationship between H2O flux and vapor pressure deficit, resulting in a change in canopy conductance, possibly due to cavitation of the tree xylem. This step change was also correlated with decreased rates of C sequestration and evapotranspiration; we estimate that this extreme climatic event decreased gross ecosystem production (GEP) by roughly 20% (4mmol C m 2 s 1 ) for the rest of the growing season. In contrast, a cooler, wetter spring in 1998 delayed the onset of photosynthesis by about 3 weeks, resulting in roughly 20% lower GEP relative to the spring of 1997. We conclude that the net C balance of Mediterranean-climate pine ecosystems is sensitive to extreme events under low soil moisture conditions and could be altered by slight changes in the climate or hydrologic regime. ©2000 Elsevier Science B.V. All rights reserved.

International Consortium for Atmospheric Research on Transport and Transformation (ICARTT): North America to Europe—Overview of the 2004 summer field study

In the summer of 2004 several separate field programs intensively studied the photochemical, heterogeneous chemical and radiative environment of the troposphere over North America, the North Atlantic Ocean, and western Europe. Previous studies have indicated that the transport of continental emissions, particularly from North America, influences the concentrations of trace species in the troposphere over the North Atlantic and Europe. An international team of scientists, representing over 100 laboratories, collaborated under the International Consortium for Atmospheric Research on Transport and Transformation (ICARTT) umbrella to coordinate the separate field programs in order to maximize the resulting advances in our understanding of regional air quality, the transport, chemical transformation and removal of aerosols, ozone, and their precursors during intercontinental transport, and the radiation balance of the troposphere. Participants utilized nine aircraft, one research vessel, several ground-based sites in North America and the Azores, a network of aerosol-ozone lidars in Europe, satellites, balloon borne sondes, and routine commercial aircraft measurements. In this special section, the results from a major fraction of those platforms are presented. This overview is aimed at providing operational and logistical information for those platforms, summarizing the principal findings and conclusions that have been drawn from the results, and directing readers to specific papers for further details.

Predicted change in global secondary organic aerosol concentrations in response to future climate, emissions, and land use change

[1] The sensitivity of secondary organic aerosol (SOA) concentration to changes in climate and emissions is investigated using a coupled global atmosphere-land model driven by the year 2100 IPCC A1B scenario predictions. The Community Atmosphere Model (CAM3) is updated with recent laboratory determined yields for SOA formation from monoterpene oxidation, isoprene photooxidation and aromatic photooxidation. Biogenic emissions of isoprene and monoterpenes are simulated interactively using the Model of Emissions of Gases and Aerosols (MEGAN2) within the Community Land Model (CLM3). The global mean SOA burden is predicted to increase by 36% in 2100, primarily the result of rising biogenic and anthropogenic emissions which independently increase the burden by 26% and 7%. The later includes enhanced biogenic SOA formation due to increased emissions of primary organic aerosol (5–25% increases in surface SOA concentrations in 2100). Climate change alone (via temperature, removal rates, and oxidative capacity) does not change the global mean SOA production, but the global burden increases by 6%. The global burden of anthropogenic SOA experiences proportionally more growth than biogenic SOA in 2100 from the net effect of climate and emissions (67% increase predicted). Projected anthropogenic land use change for 2100 (A2) is predicted to reduce the global SOA burden by 14%, largely the result of cropland expansion. South America is the largest global source region for SOA in the present day and 2100, but Asia experiences the largest relative growth in SOA production by 2100 because of the large predicted increases in Asian anthropogenic aromatic emissions. The projected decrease in global sulfur emissions implies that SOA will contribute a progressively larger fraction of the global aerosol burden.

Observed increase in local cooling effect of deforestation at higher latitudes

Deforestation in mid- to high latitudes is hypothesized to have the potential to cool the Earth’s surface by altering biophysical processes. In climate models of continental-scale land clearing, the cooling is triggered by increases in surface albedo and is reinforced by a land albedo–sea ice feedback. This feedback is crucial in the model predictions; without it other biophysical processes may overwhelm the albedo effect to generate warming instead. Ongoing land-use activities, such as land management for climate mitigation, are occurring at local scales (hectares) presumably too small to generate the feedback, and it is not known whether the intrinsic biophysical mechanism on its own can change the surface temperature in a consistent manner. Nor has the effect of deforestation on climate been demonstrated over large areas from direct observations. Here we show that surface air temperature is lower in open land than in nearby forested land. The effect is 0.85 ± 0.44 K (mean ± one standard deviation) northwards of 45° N and 0.21 ± 0.53 K southwards. Below 35° N there is weak evidence that deforestation leads to warming. Results are based on comparisons of temperature at forested eddy covariance towers in the USA and Canada and, as a proxy for small areas of cleared land, nearby surface weather stations. Night-time temperature changes unrelated to changes in surface albedo are an important contributor to the overall cooling effect. The observed latitudinal dependence is consistent with theoretical expectation of changes in energy loss from convection and radiation across latitudes in both the daytime and night-time phase of the diurnal cycle, the latter of which remains uncertain in climate models.

Fluxes of oxygenated volatile organic compounds from a ponderosa pine plantation

We present the first canopy-scale, continuous, long-term flux measurements of a suite of oxygenated volatile organic compounds (OVOCs). Fluxes were measured above a ponderosa pine plantation, adjacent to the Blodgett Forest Research Station (38°53′42.9″N, 120°37′57.9″W, 1315 m elevation), with a fully automated relaxed eddy accumulation (REA) system coupled to a dual GC-FID system. Quantified OVOCs included 2-methyl-3-buten-2-ol (MBO), methanol, ethanol, acetaldehyde, and acetone. These compounds were the most abundant nonmethane VOCs at this site and were highly correlated with each other, especially during daytime. Fluxes were dominated by MBO and methanol with daytime average emissions of ∼1.3 mg C m−2 h−1. Ethanol, acetaldehyde, and acetone fluxes were approximately a factor of 5 lower. All fluxes showed diurnal cycles with maxima around noon and minima at night. Temperature and light were the main drivers for MBO emission, and the canopy level flux responses were virtually identical with previously measured leaf level fluxes from ponderosa pine trees at the same site. Ambient temperature appeared to be the most important driver of the other OVOC fluxes, but moisture also played a role, particularly for ethanol and acetone emissions, shown for the first time under field conditions. Soil and litter emissions, measured using a Pyrex glass chamber, contributed significantly to the canopy level fluxes of methanol, acetaldehyde, and acetone, and had a much smaller contribution to the canopy fluxes of ethanol. If the magnitude of these OVOC fluxes is similar in other ecosystems, they will have to be considered a major volatile organic compound emission to the atmosphere and a potentially significant carbon loss from the biosphere.

Effects of anthropogenic emissions on aerosol formation from isoprene and monoterpenes in the southeastern United States

Significance Atmospheric secondary organic aerosol has substantial impacts on climate, air quality, and human health. However, the formation mechanisms of secondary organic aerosol remain uncertain, especially on how anthropogenic pollutants (from human activities) control aerosol formation from biogenic volatile organic compounds (emitted by vegetation) and the magnitude of anthropogenic influences. Although possible mechanisms have been proposed based on laboratories studies, a coherent understanding of anthropogenic−biogenic interactions in ambient environments has not emerged. Here, we provide direct observational evidence that secondary organic aerosol formed from biogenic isoprene and monoterpenes is greatly mediated by anthropogenic SO2 and NOx emissions based on integrated ambient measurements and laboratory studies. Secondary organic aerosol (SOA) constitutes a substantial fraction of fine particulate matter and has important impacts on climate and human health. The extent to which human activities alter SOA formation from biogenic emissions in the atmosphere is largely undetermined. Here, we present direct observational evidence on the magnitude of anthropogenic influence on biogenic SOA formation based on comprehensive ambient measurements in the southeastern United States (US). Multiple high-time-resolution mass spectrometry organic aerosol measurements were made during different seasons at various locations, including urban and rural sites in the greater Atlanta area and Centreville in rural Alabama. Our results provide a quantitative understanding of the roles of anthropogenic SO2 and NOx in ambient SOA formation. We show that isoprene-derived SOA is directly mediated by the abundance of sulfate, instead of the particle water content and/or particle acidity as suggested by prior laboratory studies. Anthropogenic NOx is shown to enhance nighttime SOA formation via nitrate radical oxidation of monoterpenes, resulting in the formation of condensable organic nitrates. Together, anthropogenic sulfate and NOx can mediate 43–70% of total measured organic aerosol (29–49% of submicron particulate matter, PM1) in the southeastern US during summer. These measurements imply that future reduction in SO2 and NOx emissions can considerably reduce the SOA burden in the southeastern US. Updating current modeling frameworks with these observational constraints will also lead to more accurate treatment of aerosol formation for regions with substantial anthropogenic−biogenic interactions and consequently improve air quality and climate simulations.