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Quantification of an ecosystem's carbon balance and its components is pivotal for understanding both ecosystem functioning and global cycling. Several methods are being applied in parallel to estimate the different components of the CO2 balance. However, different methods are subject to different sources of error. Therefore, it is necessary that site level component estimates are cross-checked against each other before being reported. Here we present a two-step approach for testing the accuracy and consistency of eddy covariance-based gross primary production (GPP) and ecosystem respiration (Re) estimates with biometric measurements of net primary production (NPP), autotrophic (Ra) and heterotrophic (Rh) respiration. The test starts with closing the CO2 balance to account for reasonable errors in each of the component fluxes. Failure to do so within the constraints will classify the flux estimates on the site level as inconsistent. If the CO2 balance can be closed, the test continues by comparing the closed site level Ra/GPP with the Rh/GPP ratio. The consistency of these ratios is then judged against expert knowledge. Flux estimates of sites that pass both steps are considered consistent. An inconsistent ratio is not necessarily incorrect but provides a signal for careful data screening that may require further analysis to identify the possible biological reasons of the unexpected ratios. We reviewed the literature and found 16 sites, out of a total of 529 research forest sites, that met the data requirements for the consistency test. Thirteen of these sites passed both steps of the consistency cross-check. Subsequently, flux ratios (NPP/GPP, Rh/NPP, Rh/Re, and Re/GPP) were calculated for the consistent sites. Similar ratios were observed at sites which lacked information to check consistency, indicating that the flux data that are currently used for validating models and testing ecological hypotheses are largely consistent across a wide range of site productivities. Confidence in the output of flux networks could be further enhanced if the required fluxes are independently estimated at all sites for multiple years and harmonized methods are used. [References: 99]

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 CO2 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 °C. 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 CO2 balance required the introduction of substantial biome-specific closure terms. Nonclosure was taken as an indication that respiratory processes, advection, and non-CO2 carbon fluxes are not presently being adequately accounted for.

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Net uptake of carbon dioxide (CO2) measured by eddy covariance in a 60- to 80-year-old forest averaged 2.0 ± 0.4 megagrams of carbon per hectare per year during 1993 to 2000, with interannual variations exceeding 50%. Biometry indicated storage of 1.6 ± 0.4 megagrams of carbon per hectare per year over 8 years, 60% in live biomass and the balance in coarse woody debris and soils, confirming eddy-covariance results. Weather and seasonal climate (e.g., variations in growing-season length or cloudiness) regulated seasonal and interannual fluctuations of carbon uptake. Legacies of prior disturbance and management, especially stand age and composition, controlled carbon uptake on the decadal time scale, implying that eastern forests could be managed for sequestration of carbon.

We used eddy covariance; gas-exchange chambers; radiocarbon analysis; wood, moss, and soil inventories; and laboratory incubations to measure the carbon balance of a 120-year-old black spruce forest in Manitoba, Canada. The site lost 0.3 ± 0.5 metric ton of carbon per hectare per year (ton C ha−1 year−1) from 1994 to 1997, with a gain of 0.6 ± 0.2 ton C ha−1year−1 in moss and wood offset by a loss of 0.8 ± 0.5 ton C ha−1 year−1 from the soil. The soil remained frozen most of the year, and the decomposition of organic matter in the soil increased 10-fold upon thawing. The stability of the soil carbon pool (∼150 tons C ha−1) appears sensitive to the depth and duration of thaw, and climatic changes that promote thaw are likely to cause a net efflux of carbon dioxide from the site.