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 C0 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 C0 2 exchange to sunlight doubles if the sky is cloudy rather than clear; 3) the spectrum of C0 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 C0 2 exchange varies with mean summer temperature; and 5) stand age affects carbon dioxide and water vapor flux densities.

Bakwin, P.; Berbigier, P.; Davis, K.; Dolman, A. J.; Falk, M.; Fuentes, J. D.; Goldstein, A.; Granier, A.; Grelle, A.; Hollinger, D.; Janssens, I. A.; Jarvis, P.; Jensen, N. O.; Katul, G.; Mahli, K.; Matteucci, G.; Meyers, T.; Monson, R.; Munger, W.; Oechel, W.; Olson, R.; Pilegaard, K.; Paw U, K. T.; Thorgeirsson, H.; Valentini, R.; Verma, Shashi; Vesala, T.; Wilson, K.; and Wofsy, S., "Environmental controls over carbon dioxide and water vapor exchange of terrestrial vegetation" (2002 B.E. Law et al. / Agricultural and Forest Meteorology 113 (2002) 97-120 AbstractThe objective of this research was to compare seasonal and annual estimates of CO 2 and water vapor exchange across sites in forests, grasslands, crops, and tundra that are part of an international network called FLUXNET, and to investigating the responses of vegetation to environmental variables. FLUXNETs goals are to understand the mechanisms controlling the exchanges of CO 2 , water vapor and energy across a spectrum of time and space scales, and to provide information for modeling of carbon and water cycling across regions and the globe. At a subset of sites, net carbon uptake (net ecosystem exchange, the net of photosynthesis and respiration) was greater under diffuse than under direct radiation conditions, perhaps because of a more efficient distribution of non-saturating light conditions for photosynthesis, lower vapor pressure deficit limitation to photosynthesis, and lower respiration associated with reduced temperature. The slope of the relation between monthly gross ecosystem production and evapotranspiration was similar between biomes, except for tundra vegetation, showing a strong linkage between carbon gain and water loss integrated over the year (slopes = 3.4 g CO 2 /kg H 2 O for grasslands, 3.2 for deciduous broadleaf forests, 3.1 for crops, 2.4 for evergreen conifers, and 1.5 for tundra vegetation). The ratio of annual ecosystem respiration to gross photosynthesis averaged 0.83, with lower values for grasslands, presumably because of less investment in respiring plant tissue compared with forests. Ecosystem respiration was weakly correlated with mean annual temperature across biomes, in spite of within site sensitivity over shorter temporal scales. Mean annual temperature and site water balance explained much of the variation in gross photosynthesis. Water availability limits leaf area index over the long-term, and inter-annual climate variability can limit carbon uptake below the potential of the leaf area present.

Deforestation in mid-to high latitudes is hypothesized to have the potential to cool the Earth's surface by altering biophysical processes [1][2][3] . 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 4,5 . This feedback is crucial in the model predictions; without it other biophysical processes may overwhelm the albedo effect to generate warming instead 5 . 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 6,7 . 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 6 0.44 K (mean 6 one standard deviation) northwards of 456 N and 0.21 6 0.53 K southwards. Below 356 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 8 .The latitudinal gradient of land-use impact is evident in the comparison of the surface air temperature recorded at FLUXNET (www.fluxnet.ornl.gov) forest towers 9 (Supplementary Table 1 and Supplementary Fig. 1) and surface weather stations in North America (Fig. 1a). Here we use the surface stations as proxies for cleared land. In accordance with the requirement of the World Meteorological Organization, these stations are located in open grassy fields that have biophysical characteristics similar to those of open land, such as being covered by snow in northern latitudes in the winter 10 . Latitude accounts for 31% of the variations in the temperature difference DT between the forest sites and the adjacent open lands (number of site pairs n 5 37). The rate of change in DT with latitude is 20.070 6 0.010 K per degree (mean 6 one standard error, s.e., P , 0.005). At these sites, the annual net all-wave radiation R n

[1] Clouds and aerosols alter the proportion of diffuse radiation in global solar radiation reaching the Earth's surface. It is known that diffuse and direct beam radiation differ in the way they transfer through plant canopies and affect the summation of nonlinear processes like photosynthesis differently than what would occur at the leaf scale. We compared the relative efficiencies of canopy photosynthesis to diffuse and direct photosynthetically active radiation (PAR) for a Scots pine forest, an aspen forest, a mixed deciduous forest, a tallgrass prairie and a winter wheat crop. The comparison was based on the seasonal patterns of the parameters that define the canopy photosynthetic responses to diffuse PAR and those that define the responses to direct PAR. These parameters were inferred from half-hourly tower CO 2 flux measurements. We found that: (1) diffuse radiation results in higher light use efficiencies by plant canopies; (2) diffuse radiation has much less tendency to cause canopy photosynthetic saturation; (3) the advantages of diffuse radiation over direct radiation increase with radiation level; (4) temperature as well as vapor pressure deficit can cause different responses in diffuse and direct canopy photosynthesis, indicating that their impacts on terrestrial ecosystem carbon assimilation may depend on radiation regimes and thus sky conditions. These findings call for different treatments of diffuse and direct radiation in models of global primary production, and studies of the roles of clouds and aerosols in global carbon cycle.

Volcanic aerosols from the 1991 Mount Pinatubo eruption greatly increased diffuse radiation worldwide for the following 2 years. We estimated that this increase in diffuse radiation alone enhanced noontime photosynthesis of a deciduous forest by 23% in 1992 and 8% in 1993 under cloudless conditions. This finding indicates that the aerosol-induced increase in diffuse radiation by the volcano enhanced the terrestrial carbon sink and contributed to the temporary decline in the growth rate of atmospheric carbon dioxide after the eruption.