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.
Heightened awareness of global change issues within both science and political communities has increased interest in using the global network of eddy covariance flux towers to more fully understand the impacts of natural and anthropogenic phenomena on the global carbon balance. Comparisons of net ecosystem exchange (F NEE ) responses are being made among biome types, phenology patterns, and stress conditions. The comparisons are usually performed on annual sums of F NEE ; however, the average data coverage during a year is only 65%. Therefore, robust and consistent gap filling methods are required.We review several methods of gap filling and apply them to data sets available from the EUROFLUX and AmeriFlux databases. The methods are based on mean diurnal variation (MDV), look-up tables (LookUp), and nonlinear regressions (Regr.), and the impact of different gap filling methods on the annual sum of F NEE is investigated. The difference between annual F NEE filled by MDV compared to F NEE filled by Regr. ranged from −45 to +200 g C m −2 per year (MDV−Regr.). Comparing LookUp and Regr. methods resulted in a difference (LookUp−Regr.) ranging from −30 to +150 g C m −2 per year.We also investigated the impact of replacing measurements at night, when turbulent mixing is insufficient. The nighttime correction for low friction velocities (u * ) shifted annual F NEE on average by +77 g C m −2 per year, but in certain cases as much as +185 g C m −2 per year.Our results emphasize the need to standardize gap filling-methods for improving the comparability of flux data products from regional and global flux networks.
Terrestrial ecosystems sequester 2.1 Pg of atmospheric carbon annually. A large amount of the terrestrial sink is realized by forests. However, considerable uncertainties remain regarding the fate of this carbon over both short and long timescales. Relevant data to address these uncertainties are being collected at many sites around the world, but syntheses of these data are still sparse. To facilitate future synthesis activities, we have assembled a comprehensive global database for forest ecosystems, which includes carbon budget variables (fluxes and stocks), ecosystem traits (e.g. leaf area index, age), as well as ancillary site information such as management regime, climate, and soil characteristics. This publicly available database can be used to quantify global, regional or biome-specific carbon budgets; to re-examine established relationships; to test emerging hypotheses about ecosystem functioning [e.g. a constant net ecosystem production (NEP) to gross primary production (GPP) ratio]; and as benchmarks for model evaluations. In this paper, we present the first analysis of this database. We discuss the climatic influences on GPP, net primary production (NPP) and NEP and present the CO 2 balances for boreal, temperate, and tropical forest biomes based on micrometeorological, ecophysiological, and biometric flux and inventory estimates. Globally, GPP of forests benefited from higher temperatures and precipitation whereas NPP saturated above either a threshold of 1500 mm precipitation or a mean annual temperature of 10 1C. The global pattern in NEP was insensitive to climate and is hypothesized to be mainly determined by nonclimatic conditions such as successional stage, management, site history, and site disturbance. In all biomes, closing the CO 2 balance required the introduction of substantial biome-specific closure terms. Nonclosure was taken as an indication that respiratory processes, advection, and non-CO 2 carbon fluxes are not presently being adequately accounted for. Nomenclauture:DOC 5 dissolved organic carbon; fNPP 5 foliage component of NPP; GPP 5 gross primary production (GPP40 denotes photosynthetic uptake); mNPP 5 missing component of NPP;NBP 5 net biome production (NBP40 denotes biome uptake); NECB 5 net ecosystem carbon balance (NECB40 denotes ecosystem uptake); NEE 5 net ecosystem exchange (NEE40 denotes ecosystem uptake); NEP 5 net ecosystem production (NEP40 denotes ecosystem uptake); NPP 5 net primary production (NPP40 denotes ecosystem uptake); R a 5 autotrophic respiration (R a 40 denotes respiratory losses); R e 5 ecosystem respiration (R e 40 denotes respiratory losses); R h 5 heterotrophic respiration (R h 40 denotes respiratory losses); rNPP 5 root component of NPP;R s 5 soil respiration (R s 40 denotes respiratory losses); VOC 5 volatile organic compounds; wNPP 5 wood component of NPP
Terrestrial plants remove CO2 from the atmosphere through photosynthesis, a process that is accompanied by the loss of water vapour from leaves. The ratio of water loss to carbon gain, or water-use efficiency, is a key characteristic of ecosystem function that is central to the global cycles of water, energy and carbon. Here we analyse direct, long-term measurements of whole-ecosystem carbon and water exchange. We find a substantial increase in water-use efficiency in temperate and boreal forests of the Northern Hemisphere over the past two decades. We systematically assess various competing hypotheses to explain this trend, and find that the observed increase is most consistent with a strong CO2 fertilization effect. The results suggest a partial closure of stomata-small pores on the leaf surface that regulate gas exchange-to maintain a near-constant concentration of CO2 inside the leaf even under continually increasing atmospheric CO2 levels. The observed increase in forest water-use efficiency is larger than that predicted by existing theory and 13 terrestrial biosphere models. The increase is associated with trends of increasing ecosystem-level photosynthesis and net carbon uptake, and decreasing evapotranspiration. Our findings suggest a shift in the carbon- and water-based economics of terrestrial vegetation, which may require a reassessment of the role of stomatal control in regulating interactions between forests and climate change, and a re-evaluation of coupled vegetation-climate models.
The carbon balance of terrestrial ecosystems is particularly sensitive to climatic changes in autumn and spring, with spring and autumn temperatures over northern latitudes having risen by about 1.1 degrees C and 0.8 degrees C, respectively, over the past two decades. A simultaneous greening trend has also been observed, characterized by a longer growing season and greater photosynthetic activity. These observations have led to speculation that spring and autumn warming could enhance carbon sequestration and extend the period of net carbon uptake in the future. Here we analyse interannual variations in atmospheric carbon dioxide concentration data and ecosystem carbon dioxide fluxes. We find that atmospheric records from the past 20 years show a trend towards an earlier autumn-to-winter carbon dioxide build-up, suggesting a shorter net carbon uptake period. This trend cannot be explained by changes in atmospheric transport alone and, together with the ecosystem flux data, suggest increasing carbon losses in autumn. We use a process-based terrestrial biosphere model and satellite vegetation greenness index observations to investigate further the observed seasonal response of northern ecosystems to autumnal warming. We find that both photosynthesis and respiration increase during autumn warming, but the increase in respiration is greater. In contrast, warming increases photosynthesis more than respiration in spring. Our simulations and observations indicate that northern terrestrial ecosystems may currently lose carbon dioxide in response to autumn warming, with a sensitivity of about 0.2 PgC degrees C(-1), offsetting 90% of the increased carbon dioxide uptake during spring. If future autumn warming occurs at a faster rate than in spring, the ability of northern ecosystems to sequester carbon may be diminished earlier than previously suggested.
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
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