Environmental change and the carbon balance of Amazonian forests

Extreme climatic events and land‐use change are known to influence strongly the current carbon cycle of Amazonia, and have the potential to cause significant global climate impacts. This review intends to evaluate the effects of both climate and anthropogenic perturbations on the carbon balance of the Brazilian Amazon and to understand how they interact with each other. By analysing the outputs of the Intergovernmental Panel for Climate Change (IPCC) Assessment Report 4 (AR4) model ensemble, we demonstrate that Amazonian temperatures and water stress are both likely to increase over the 21st Century. Curbing deforestation in the Brazilian Amazon by 62% in 2010 relative to the 1990s mean decreased the Brazilian Amazon's deforestation contribution to global land use carbon emissions from 17% in the 1990s and early 2000s to 9% by 2010. Carbon sources in Amazonia are likely to be dominated by climatic impacts allied with forest fires (48.3% relative contribution) during extreme droughts. The current net carbon sink (net biome productivity, NBP) of +0.16 (ranging from +0.11 to +0.21) Pg C year^?1 in the Brazilian Amazon, equivalent to 13.3% of global carbon emissions from land‐use change for 2008, can be negated or reversed during drought years [NBP = ?0.06 (?0.31 to +0.01) Pg C year^?1]. Therefore, reducing forest fires, in addition to reducing deforestation, would be an important measure for minimizing future emissions. Conversely, doubling the current area of secondary forests and avoiding additional removal of primary forests would help the Amazonian gross forest sink to offset approximately 42% of global land‐use change emissions. We conclude that a few strategic environmental policy measures are likely to strengthen the Amazonian net carbon sink with global implications. Moreover, these actions could increase the resilience of the net carbon sink to future increases in drought frequency.     

Biometric-based estimation of net ecosystem production in a mature Japanese cedar (<Emphasis Type="Italic">Cryptomeria japonica</Emphasis>) plantation beneath a flux tower

Quantification of carbon budgets and cycling in Japanese cedar (Cryptomeria japonica D. Don) plantations is essential for understanding forest functions in Japan because these plantations occupy about 20% of the total forested area. We conducted a biometric estimate of net ecosystem production (NEP) in a mature Japanese cedar plantation beneath a flux tower over a 4-year period. Net primary production (NPP) was 7.9 Mg C ha⁻¹ year⁻¹ and consisted mainly of tree biomass increment and aboveground litter production. Respiration was calculated as 6.8 (soil) and 3.3 (root) Mg C ha⁻¹ year⁻¹. Thus, NEP in the plantation was 4.3 Mg C ha⁻¹ year⁻¹. In agreement with the tower-based flux findings, this result suggests that the Japanese cedar plantation was a strong carbon sink. The biometric-based NEP was higher among most other types of Japanese forests studied. Carbon sequestration in the mature plantation was characterized by a larger increment in tree biomass and lower mortality than in natural forests. Land-use change from natural forest to Japanese cedar plantation might, therefore, stimulate carbon sequestration and change the carbon allocation of NPP from an increment in coarse woody debris to an increase in tree biomass.     

Biometric Based Carbon Flux Measurements and Net Ecosystem Production (NEP) in a Temperate Deciduous Broad-Leaved Forest Beneath a Flux Tower

Biometric based carbon flux measurements were conducted over 5 years (1999–2003) in a temperate deciduous broad-leaved forest of the AsiaFlux network to estimate net ecosystem production (NEP). Biometric based NEP, as measured by the balance between net primary production (including NPP of canopy trees and of forest floor dwarf bamboo) and heterotrophic respiration (RH), clarified the contribution of various biological processes to the ecosystem carbon budget, and also showed where and how the forest is storing C. The mean NPP of the trees was 5.4 ± 1.07 t C ha⁻¹ y⁻¹, including biomass increment (0.3 ± 0.82 t C ha⁻¹ y⁻¹), tree mortality (1.0 ± 0.61 t C ha⁻¹ y⁻¹), aboveground detritus production (2.3 ± 0.39 t C ha⁻¹ y⁻¹) and belowground fine root production (1.8 ± 0.31 t C ha⁻¹ y⁻¹). Annual biomass increment was rather small because of high tree mortality during the 5 years. Total NPP at the site was 6.5 ± 1.07 t C ha⁻¹ y⁻¹, including the NPP of the forest floor community (1.1 ± 0.06 t C ha⁻¹ y⁻¹). The soil surface CO₂ efflux (RS) was averaged across the 5 years of record using open-flow chambers. The mean estimated annual RS amounted to 7.1 ± 0.44 t C ha⁻¹, and the decomposition of soil organic matter (SOM) was estimated at 3.9 ± 0.24 t C ha⁻¹. RH was estimated at 4.4 ± 0.32 t C ha⁻¹ y⁻¹, which included decomposition of coarse woody debris. Biometric NEP in the forest was estimated at 2.1 ± 1.15 t C ha⁻¹ y⁻¹, which agreed well with the eddy-covariance based net ecosystem exchange (NEE). The contribution of woody increment (Δbiomass + mortality) of the canopy trees to NEP was rather small, and thus the SOM pool played an important role in carbon storage in the temperate forest. These results suggested that the dense forest floor of dwarf bamboo might have a critical role in soil carbon sequestration in temperate East Asian deciduous forests.     

Woody debris contribution to the carbon budget of selectively logged and maturing mid-latitude forests

Woody debris (WD) is an important component of forest C budgets, both as a C reservoir and source of CO₂ to the atmosphere. We used an infrared gas analyzer and closed dynamic chamber to measure CO₂ efflux from downed coarse WD (CWD; diameter≥7.5 cm) and fine WD (FWD; 7.5 cm>diameter≥2 cm) to assess respiration in a selectively logged forest and a maturing forest (control site) in the northeastern USA. We developed two linear regression models to predict WD respiration: one based on WD temperature, moisture, and size (R ²=0.57), and the other on decay class and air temperature (R ²=0.32). WD respiration (0.28±0.09 Mg C ha⁻¹ year⁻¹) contributed only ≈2% of total ecosystem respiration (12.3±0.7 Mg C ha⁻¹ year⁻¹, 1999–2003), but net C flux from CWD accounted for up to 30% of net ecosystem exchange in the maturing forest. C flux from CWD on the logged site increased modestly, from 0.61±0.29 Mg C ha⁻¹ year⁻¹ prior to logging to 0.77±0.23 Mg C ha⁻¹ year⁻¹ after logging, reflecting increased CWD stocks. FWD biomass and associated respiration flux were ≈7 times and ≈5 times greater, respectively, in the logged site than the control site. The net C flux associated with CWD, including inputs and respiratory outputs, was 0.35±0.19 Mg C ha⁻¹ year⁻¹ (net C sink) in the control site and −0.30±0.30 Mg C ha⁻¹ year⁻¹ (net C source) in the logged site. We infer that accumulation of WD may represent a small net C sink in maturing northern hardwood forests. Disturbance, such as selective logging, can enlarge the WD pool, increasing the net C flux from the WD pool to the atmosphere and potentially causing it to become a net C source.Electronic Supplementary Material Supplementary material is available for this article at and is accessible for authorized users.     

Carbon Pools and Emissions from Deforestation in Extra-Tropical Forests of Northern Argentina Between 1900 and 2005

We estimated carbon pools and emissions from deforestation in northern Argentine forests between 1900 and 2005, based on forest inventories, deforestation estimates from satellite images and historical data on forests and agriculture. Carbon fluxes were calculated using a book-keeping model. We ran 1000 simulations for a 105-year period with different combinations of values of carbon stocks (Mg C ha⁻¹), soil carbon in the top 0.2 m, and annual deforestation series. The 1000 combinations of parameters were performed as a sensitivity analysis that for each run, randomly selected the values of each variable within a predefined range of values and probability distributions. Using the simulation outputs, we calculated the accumulated C emissions due to deforestation from 1900 to 2005 and the annual emission as the average of the 1000 simulations, and uncertainties of our estimates as the standard deviation. We found that northern Argentine forests contain an estimated 4.54 Pg C (2.312 Pg C in biomass and 2.233 Pg C in soil). Between 1900 and 2005 approximately 30% of the forests were deforested, yielding carbon emissions of 0.945 (SD = 0.270) Pg C. Estimated average annual carbon emissions between 1996 and 2005, mostly from deforestation of the Chaco dry forests, were 20,875 (SD = 6,156) Gg C y⁻¹ (1 Gg = 10⁻⁶ Pg). These values represent the largest source of carbon from land-cover change in the extra-tropical southern hemisphere, between 0.9 and 2.7% of the global carbon emissions from deforestation, and approximately 10% of carbon emissions from the Brazilian Amazon. Deforestation, which has accelerated during the last decades as a result of modern agriculture expansion, represents a major national source of greenhouse gases and the second emission source, after fossil fuel consumption by fixed sources. We conclude that Argentine forests are an important carbon pool and emission source that need more attention for accurate global estimates, and seasonally dry forest deforestation is a key component of the Argentine carbon cycle. Electronic supplementary material  The online version of this article (doi:) contains supplementary material, which is available to authorized users.     

Different patterns of ecosystem carbon accumulation between a young and an old-growth subtropical forest in Southern China

Using long-term (22 years) measurements from a young and an old-growth subtropical forest in southern China, we found that both forests accumulated carbon from 1982 to 2004, with the mean carbon accumulation rate at 227 ± 59 g C m⁻² year⁻¹ for young forest and 115 ± 89 g C m⁻² year⁻¹ for the old-growth forest. Allocation of the accumulated carbon was quite different between these two forests: the young forest accumulated a significant amount of carbon in plant live biomass, whereas the old-growth forest accumulated a significant amount of carbon in the soil. From 1982 to 2004, net primary productivity (NPP) increased for the young forest, and did not change significantly for the old-growth forest. The increase in NPP of the young forest resulted from recruitment of some dominant tree species characteristic of the subtropical mature forest in the region and an increase in tree density; decline of NPP of the old-growth forest was caused by increased mortality of the dominant trees.     

Soil respiration of forest ecosystems in Japan and global implications

Within terrestrial ecosystems, soil respiration is one of the largest carbon flux components. We discuss the factors controlling soil respiration, while focusing on research conducted at the Takayama Experimental Site. Soil respiration was affected by soil temperature, soil moisture, rainfall events, typhoons, and root respiration. We consider the temporal and spatial variability of soil respiration at the Takayama Experimental Site and review the variability of annual soil respiration in Japanese forests. In the 26 compiled studies, the values of annual soil respiration ranged from 203 to 1,290 g C m⁻² year⁻¹, with a mean value of 669 g C m⁻² year⁻¹ (SD=264, CV=40). We note the need for more studies and data synthesis for the accurate prediction of soil respiration and soil carbon dynamics in Japanese forests. Finally, several methods for measuring soil respiration rates are compared and the implications of soil respiration rates for global climate change are discussed.     

Pools and fluxes of carbon in three Norway spruce ecosystems along a climatic gradient in Sweden

This paper presents an integrated analysis of organic carbon (C) pools in soils and vegetation, within-ecosystem fluxes and net ecosystem exchange (NEE) in three 40-year old Norway spruce stands along a north-south climatic gradient in Sweden, measured 2001–2004. A process-orientated ecosystem model (CoupModel), previously parameterised on a regional dataset, was used for the analysis. Pools of soil organic carbon (SOC) and tree growth rates were highest at the southernmost site (1.6 and 2.0-fold, respectively). Tree litter production (litterfall and root litter) was also highest in the south, with about half coming from fine roots (<1 mm) at all sites. However, when the litter input from the forest floor vegetation was included, the difference in total litter input rate between the sites almost disappeared (190–233 g C m⁻² year⁻¹). We propose that a higher N deposition and N availability in the south result in a slower turnover of soil organic matter than in the north. This effect seems to overshadow the effect of temperature. At the southern site, 19% of the total litter input to the O horizon was leached to the mineral soil as dissolved organic carbon, while at the two northern sites the corresponding figure was approx. 9%. The CoupModel accurately described general C cycling behaviour in these ecosystems, reproducing the differences between north and south. The simulated changes in SOC pools during the measurement period were small, ranging from −8 g C m⁻² year⁻¹ in the north to +9 g C m⁻² year⁻¹ in the south. In contrast, NEE and tree growth measurements at the northernmost site suggest that the soil lost about 90 g C m⁻² year⁻¹. An erratum to this article can be found at     

Carbon stock and cycling in a bambooPhyllostachys bambusoides stand

Gross production and carbon cycling in aPhyllostachys bambusoides stand in Kyoto Prefecture, central Japan, were determined, and then a compartment model showing the carbon stock and cycling within the ecosystem was developed. Aboveground carbon stock was 52.3 tC ha⁻¹, increasing at a rate of 3.6 tC ha⁻¹ year⁻¹. Belowground carbon stock was 20.8 tC ha⁻¹ in the root system and 92.0 tC ha⁻¹ in the soil. Aboveground net production was 11.2 tC ha⁻¹ year⁻¹. Belowground net production was crudely estimated at 4.5 tC ha⁻¹ year⁻¹. The gross production was estimated at 41.8 tC ha⁻¹ year⁻¹ by summing the amount of outflow to the environment and the increment in biomass. Leaves consumed 13.7 tC ha⁻¹ year⁻¹ by respiration; the rest (41.8−13.7=28.1 tC ha⁻¹ year⁻¹) was surplus production of the leaves and flowed into the other compartments. The amounts of construction and maintenance respiration of the aboveground compartments were 3.4 and 18.5 tC ha⁻¹ year⁻¹, respectively. The annual amount of soil respiration was 11.2 tC ha⁻¹ year⁻¹. Soil respiration levels of 4.3 and 3.1 tC ha⁻¹ year⁻¹ were estimated for the flow of root respiration and root detritus. The proportion of net to gross production was 37%, which fell within the range of young and mature forests. A shorter life span of culms, compared to tree trunks, resulted in smaller biomass accumulation ratio (biomass/net production) in the ecosystem, of 4.66.     

Regional application of an ecosystem production model for studies of biogeochemistry in Brazilian Amazonia

The degree to which primary production, soil carbon, and trace gas fluxes in tropical forests of the Amazon are limited by moisture availability and other environmental factors was examined using an ecosystem modelling application for the country of Brazil. A regional geographical information system (GIS) serves as the data source of climate drivers, satellite images, land cover, and soil properties for input to the NASA Ames-CASA (Carnegie-Ames-Stanford Approach) model over a 8-km grid resolution. Simulation results lead us to hypothesize that net primary production (NPP) is limited by cloud interception of solar radiation over the humid north-western portion of the region. Peak annual rates for NPP of nearly 1.4 kg C m^–2 year^–1 are localized in the seasonally dry eastern Amazon in areas that we assume are primarily deep-rooted evergreen forest cover. Regional effects of forest conversion on NPP and soil carbon content are indicated in the model results, especially in seasonally dry areas. Comparison of model flux predictions along selected eco-climatic transects reveal moisture, soil, and land use controls on gradients of ecosystem production and soil trace gas emissions (CO₂, N₂O, and NO). These results are used to formulate a series of research hypotheses for testing in the next phase of regional modelling, which includes recalibration of the light-use efficiency term in NASA-CASA using field measurements of NPP, and refinements of vegetation index and soil property (texture and potential rooting depth) maps for the region.     

Modelling temporal variability in the carbon balance of a spruce/moss boreal forest

A model of the daily carbon balance of a black spruce/feathermoss boreal forest ecosystem was developed and results compared to preliminary data from the 1994 BOREAS field campaign in northem Manitoba, Canada. The model, driven by daily weather conditions, simulated daily soil climate status (temperature and moisture profiles), spruce photosynthesis and respiration, moss photosynthesis and respiration, and litter decomposition. Model agreement with preliminary field data was good for net ecosystem exchange (NEE), capturing both the asymmetrical seasonality and short-term variability. During the growing season simulated daily NEE ranged from -4 g C m^-2 d^-1 (carbon uptake by ecosystem) to + 2 g C m^-2 d^-1 (carbon flux to atmosphere), with fluctuations from day to day. In the early winter simulated NEE values were + 0.5 g C m^-2 d^-1, dropping to + 0.2 g C m^-2 d^-1 in mid-winter. Simulated soil respiration during the growing season (+ 1 to + 5 g C m^-2 d^-1) was dominated by metabolic respiration of the live moss, with litter decomposition usually contributing less than 30% and live spruce root respiration less than 10% of the total. Both spruce and moss net primary productivity (NPP) rates were higher in early summer than late summer. Simulated annual NEE for 1994 was -51 g C m^-2 y^-1, with 83% going into tree growth and 17% into the soil carbon accumulation. Moss NPP (58 g C m^-2 y^-1) was considered to be litter (i.e. soil carbon input; no net increase in live moss biomass). Ecosystem respiration during the snow-covered season (84 g C m^-2) was 58% of the growing season net carbon uptake. A simulation of the same site for 1968–1989 showed = 10–20% year-to-year variability in heterotrophic respiration (mean of + 113 g C m^-2 y^-1). Moss NPP ranged from 19 to 114 g C m^-2 y^-1; spruce NPP from 81 to 150 g C m^-2 y^-1; spruce growth (NPP minus litterfall) from 34 to 103 g C m^-2 y^-1; NEE ranged from +37 to -142 g C m^-2 y^-1. Values for these carbon balance terms in 1994 were slightly smaller than the 1969–89 means. Higher ecosystem productivity years (more negative NEE) generally had early springs and relatively wet summers; lower productivity years had late springs and relatively dry summers.     

FLUXNET and modelling the global carbon cycle

Measurements of the net CO₂ flux between terrestrial ecosystems and the atmosphere using the eddy covariance technique have the potential to underpin our interpretation of regional CO₂ source–sink patterns, CO₂ flux responses to forcings, and predictions of the future terrestrial C balance. Information contained in FLUXNET eddy covariance data has multiple uses for the development and application of global carbon models, including evaluation/validation, calibration, process parameterization, and data assimilation. This paper reviews examples of these uses, compares global estimates of the dynamics of the global carbon cycle, and suggests ways of improving the utility of such data for global carbon modelling. Net ecosystem exchange of CO₂ (NEE) predicted by different terrestrial biosphere models compares favourably with FLUXNET observations at diurnal and seasonal timescales. However, complete model validation, particularly over the full annual cycle, requires information on the balance between assimilation and decomposition processes, information not readily available for most FLUXNET sites. Site history, when known, can greatly help constrain the model‐data comparison. Flux measurements made over four vegetation types were used to calibrate the land‐surface scheme of the Goddard Institute for Space Studies global climate model, significantly improving simulated climate and demonstrating the utility of diurnal FLUXNET data for climate modelling. Land‐surface temperatures in many regions cool due to higher canopy conductances and latent heat fluxes, and the spatial distribution of CO₂ uptake provides a significant additional constraint on the realism of simulated surface fluxes. FLUXNET data are used to calibrate a global production efficiency model (PEM). This model is forced by satellite‐measured absorbed radiation and suggests that global net primary production (NPP) increased 6.2% over 1982–1999. Good agreement is found between global trends in NPP estimated by the PEM and a dynamic global vegetation model (DGVM), and between the DGVM and estimates of global NEE derived from a global inversion of atmospheric CO₂ measurements. Combining the PEM, DGVM, and inversion results suggests that CO₂ fertilization is playing a major role in current increases in NPP, with lesser impacts from increasing N deposition and growing season length. Both the PEM and the inversion identify the Amazon basin as a key region for the current net terrestrial CO₂ uptake (i.e. 33% of global NEE), as well as its interannual variability. The inversion's global NEE estimate of −1.2 Pg [C] yr⁻¹ for 1982–1995 is compatible with the PEM‐ and DGVM‐predicted trends in NPP. There is, thus, a convergence in understanding derived from process‐based models, remote‐sensing‐based observations, and inversion of atmospheric data. Future advances in field measurement techniques, including eddy covariance (particularly concerning the problem of night‐time fluxes in dense canopies and of advection or flow distortion over complex terrain), will result in improved constraints on land‐atmosphere CO₂ fluxes and the rigorous attribution of mechanisms to the current terrestrial net CO₂ uptake and its spatial and temporal heterogeneity. Global ecosystem models play a fundamental role in linking information derived from FLUXNET measurements to atmospheric CO₂ variability. A number of recommendations concerning FLUXNET data are made, including a request for more comprehensive site data (particularly historical information), more measurements in undisturbed ecosystems, and the systematic provision of error estimates. The greatest value of current FLUXNET data for global carbon cycle modelling is in evaluating process representations, rather than in providing an unbiased estimate of net CO₂ exchange.     

Global Validation of a Process-Based Model on Vegetation Gross Primary Production Using Eddy Covariance Observations

Gross Primary Production (GPP) is the largest flux in the global carbon cycle. However, large uncertainties in current global estimations persist. In this study, we examined the performance of a process-based model (Integrated BIosphere Simulator, IBIS) at 62 eddy covariance sites around the world. Our results indicated that the IBIS model explained 60% of the observed variation in daily GPP at all validation sites. Comparison with a satellite-based vegetation model (Eddy Covariance-Light Use Efficiency, EC-LUE) revealed that the IBIS simulations yielded comparable GPP results as the EC-LUE model. Global mean GPP estimated by the IBIS model was 107.50±1.37 Pg C year⁻¹ (mean value ± standard deviation) across the vegetated area for the period 2000–2006, consistent with the results of the EC-LUE model (109.39±1.48 Pg C year⁻¹). To evaluate the uncertainty introduced by the parameter V_cmax, which represents the maximum photosynthetic capacity, we inversed V_cmax using Markov Chain-Monte Carlo (MCMC) procedures. Using the inversed V_cmax values, the simulated global GPP increased by 16.5 Pg C year⁻¹, indicating that IBIS model is sensitive to V_cmax, and large uncertainty exists in model parameterization.     

Culm recruitment,dry matter dynamics and carbon flux in recently harvested and mature bamboo savannas in the Indian dry tropics

Culm recruitment, standing crop biomass, net production and carbon flux were estimated in mature (5 years after last harvest) and recently harvested bamboo (Dendrocalamus strictus (Roxb.) Nees) savanna sites in the dry tropics. During the 2 study years bamboo shoot recruitment was 1711–3182 and 1432–1510 shoots ha⁻¹ in harvested and mature sites, respectively. Corresponding shoot mortality was 66–93% and 62–69%, respectively. Total biomass was 34.9 t ha⁻¹ at the harvested site and 47.4 t ha⁻¹ at the mature site. Harvesting increased the relative contribution of belowground bamboo biomass. Annual litter input to soil was 2.7 and 5.9 t ha⁻¹ year⁻¹ at the harvested and mature sites, respectively. The bulk of the annual litterfall (78–88%) occurred in the cool dry season (November to February). The mean litter mass on the savanna floor ranged from 3.1 to 3.3 t ha⁻¹; at the harvested site wood litter contributed 70% of the litter mass and at the mature site leaves formed 77% of the litter mass. The mean total net production (TNP) for the two annual cycles was 15.8 t ha⁻¹ year⁻¹ at the harvested site and 19.3 t ha⁻¹ year⁻¹ at the mature site. Nearly half (46–57%) of the TNP was allocated to the belowground parts. Short lived components (leaves and fine roots) contributed about four-fifths of the net production of bamboo. Total carbon storage in the system was 64.4 t ha⁻¹ at the harvested site and 75.4 t ha⁻¹ at the mature site, of which 23–28% was distributed in vegetation, 2% in litter and 70–75% in soil. Annual net carbon deposition was 6.3 and 8.7 t ha⁻¹ year⁻¹ at harvested and mature sites, respectively.     

Tropical wetlands: seasonal hydrologic pulsing,carbon sequestration,and methane emissions

This paper summarizes the importance of climate on tropical wetlands. Regional hydrology and carbon dynamics in many of these wetlands could shift with dramatic changes in these major carbon storages if the inter-tropical convergence zone (ITCZ) were to change in its annual patterns. The importance of seasonal pulsing hydrology on many tropical wetlands, which can be caused by watershed activities, orographic features, or monsoonal pulses from the ITCZ, is illustrated by both annual and 30-year patterns of hydrology in the Okavango Delta in southern Africa. Current studies on carbon biogeochemistry in Central America are attempting to determine the rates of carbon sequestration in tropical wetlands compared to temperate wetlands and the effects of hydrologic conditions on methane generation in these wetlands. Using the same field and lab techniques, we estimated that a humid tropical wetland in Costa Rica accumulated 255 g C m⁻² year⁻¹ in the past 42 years, 80% more than a similar temperate wetland in Ohio that accumulated 142 g C m⁻² year⁻¹ over the same period. Methane emissions averaged 1,080 mg-C m⁻² day⁻¹ in a seasonally pulsed wetland in western Costa Rica, a rate higher than methane emission rates measured over the same period from humid tropic wetlands in eastern Costa Rica (120–278 mg-C m⁻² day⁻¹). Tropical wetlands are often tuned to seasonal pulses of water caused by the seasonal movement of the ITCZ and are the most likely to be have higher fire frequency and changed methane emissions and carbon oxidation if the ITCZ were to change even slightly.     

Contribution of Sediment Respiration to Summer CO2 Emission from Low Productive Boreal and Subarctic Lakes

We measured sediment production of carbon dioxide (CO₂) and methane (CH₄) and the net flux of CO₂ across the surfaces of 15 boreal and subarctic lakes of different humic contents. Sediment respiration measurements were made in situ under ambient light conditions. The flux of CO₂ between sediment and water varied between an uptake of 53 and an efflux of 182 mg C m⁻² day⁻¹ from the sediments. The mean respiration rate for sediments in contact with the upper mixed layer (SedR) was positively correlated to dissolved organic carbon (DOC) concentration in the water (r² = 0.61). The net flux of CO₂ across the lake surface [net ecosystem exchange (NEE)] was also closely correlated to DOC concentration in the upper mixed layer (r² = 0.73). The respiration in the water column was generally 10-fold higher per unit lake area compared to sediment respiration. Lakes with DOC concentrations <5.6 mg L⁻¹ had net consumption of CO₂ in the sediments, which we ascribe to benthic primary production. Only lakes with very low DOC concentrations were net autotrophic (<2.6 mg L⁻¹) due to the dominance of dissolved allochthonous organic carbon in the water as an energy source for aquatic organisms. In addition to previous findings of allochthonous organic matter as an important driver of heterotrophic metabolism in the water column of lakes, this study suggests that sediment metabolism is also highly dependent on allochthonous carbon sources.     

Soil Nutrients Limit Fine Litter Production and Tree Growth in Mature Lowland Forest of Southwestern Borneo

Efforts to improve models of terrestrial productivity and to understand the function of tropical forests in global carbon cycles require a mechanistic understanding of spatial variation in aboveground net primary productivity (ANPP) across tropical landscapes. To help derive such an understanding for Borneo, we monitored aboveground fine litterfall, woody biomass increment and ANPP (their sum) in mature forest over 29 months across a soil nutrient gradient in southwestern Kalimantan. In 30 (0.07 ha) plots stratified throughout the watershed (∼340 ha, 8–190 m a.s.l.), we measured productivity and tested its relationship with 27 soil parameters. ANPP across the study area was among the highest reported for mature lowland tropical forests. Aboveground fine litterfall ranged from 5.1 to 11.0 Mg ha⁻¹ year⁻¹ and averaged 7.7 ± 0.4 (mean ± 95 C.I.). Woody biomass increment ranged from 5.8 to 23.6 Mg ha⁻¹ year⁻¹ and averaged 12.0 ± 2.0. Growth of large trees (≥60 cm dbh) contributed 38–82% of plot-wide biomass increment and explained 92% of variation among plots. ANPP, the sum of these parameters, ranged from 11.1 to 32.3 Mg ha⁻¹ year⁻¹ and averaged 19.7 ± 2.2. ANPP was weakly related to fine litterfall (r ² = 0.176), but strongly related to growth of large trees at least 60 cm dbh (r ² = 0.848). Adjusted ANPP after accounting for apparent “mature forest bias” in our sampling method was 17.5 ± 1.2 Mg ha⁻¹ year⁻¹.Relating productivity measures to soil parameters showed that spatial patterning in productivity was significantly related to soil nutrients, especially phosphorus (P). Fine litterfall increased strongly with extractable P (r ² = 0.646), but reached an asymptote at moderate P levels, whereas biomass increment (r ² = 0.473) and ANPP (r ² = 0.603) increased linearly across the gradient. Biomass increment of large trees was more frequently and strongly related to nutrients than small trees, suggesting size dependency of tree growth on nutrients. Multiple linear regression confirmed the leading importance of soil P, and identified Ca as a potential co-limiting factor. Our findings strongly suggest that (1) soil nutrients, especially P, limit aboveground productivity in lowland Bornean forests, and (2) these forests play an important, but changing role in carbon cycles, as canopy tree logging alters these terrestrial carbon sinks. Electronic supplementary material The online version of this article (doi:) contains supplementary material, which is available to authorized users.     

Species Structure, Dry Matter Dynamics and Carbon Flux of a Dry Tropical Forest in India

Species composition, plant biomass and net primary productivitywere studied on three sites of a dry tropical forest The forestwas characterized by small structure with 38–10.4 m2 ha^–1tree and 3 1–7 8 m² ha^–1 shrub basal cover Speciesdiversity was highest for the mid-slope site while the concentrationof dominance was greatest for the hill-top stand The beta diversitywas 3 1 Total standing crop of vegetation averaged 66 98 t ha^–1with 46 70 t ha^–1 in the tree layer, 13.97 t ha^–1in the shrub layer, 0.35 t ha^–1 in the herb layer, 2 83t ha^–1 in the litter layer and 3 13 t ha^–1 in fineroots Of the total annual litterfall (4 88–6.71 t ha^–1),69% was accounted for by leaves and 31% by non-leaf matter Netprimary production (NPP) ranged between 11 3 and 19 2 t ha^–1year^–1, to which the contributions of trees, shrubs andherbs averaged 72, 22 and 6%, respectively Contribution of rootsto NPP was substantial and ranged from 2 9 to 5 3 t ha^–1year^–1 A total of 83% of vegetation carbon was storedin the above-ground plant parts while the above-ground NPP wasresponsible for 72% of the total carbon input into the systemThe contribution of foliage, herbaceous vegetation and fineroots to carbon turnover was disproportionately larger comparedto their share in the total standing crop Carbon budgeting indicatedthat the forest was an accumulating system, over at least theshort term Dry tropical forest, biomass, litterfall, net primary production, carbon budget, carbon flux     

Characteristics of net ecosystem carbon dioxide exchange (NEE) from August to October of Alpine meadow on the Tibetan Plateau, China

The Alpine meadow is one of the vegetation types widely distributed on the Tibetan Plateau in China with an area of about 1.2 million square kilometers. The Damxung rangeland station, located in the hinterland of the Tibetan Plateau, is covered with an typical vegetation. The continuous carbon flux data (from August to middle October, 2003) measured with the open-path eddy covariance system was used to analyze the diurnal variation pattern of net ecosystem carbon dioxide exchange (NEE) and its relationship with the environmental factors, such as photosynthetically active radiation (PAR), precipitation, and temperature. Results showed that NEE presented obvious diurnal variation pattern with single-peak of diurnal maximum carbon assimilation at 11: 00–12: 00 (local time) with an average of −0.268 mg CO₂·m⁻²·s⁻¹, i.e., −6.08 μmol CO₂·m⁻²·s⁻¹. During the daytime, NEE fitted fairly well with PAR in a rectangular hyperbola function with the apparent quantum yield (0.020 3 μmol CO₂ μmol⁻¹ PAR) and maximum ecosystem assimilation (9.741 1 μmol CO₂·m⁻²·s⁻¹). During the night-time, NEE showed a good exponential relation with the soil temperature at 5 cm depth. __________ Translated from Acta Ecologica Sinica 2005, 25(8): 1948–1952 [译自: 生态学报, 2005, 25(8): 1948–1952]     

A Tropical Freshwater Wetland: II. Production,Decomposition, and Peat Formation

As much as 10% of the total carbon stored in peatlands occurs in the tropics. Although tropical peatlands are poorly understood scientifically, they are increasingly exploited for a variety of human uses. Our objective was to measure baseline carbon cycling data in one type of tropical peatland in order to understand better how peat accumulates in these ecosystems. Average plant production for two study sites on the island of Kosrae in the Federated States of Micronesia over 2 year was 1122 g C m⁻² year⁻¹, of which 1058 g C m⁻² year⁻¹ was aboveground plant production (bole, buttress and litterfall). Although leaves contributed a high proportion of total plant productivity, their rapid decomposition left little carbon for peat accumulation. In contrast, fine roots only contributed 10% to plant productivity, but their slow decomposition allowed them to accumulate as peat. Wood (branches and stems) probably contributed the most carbon to the formation of peat. Despite being on the soil surface, small branches decomposed more slowly than leaves because of their high C:N and lignin:N ratios. In summary, we suggest that tropical peatlands in Micronesia accumulate peat not because of high plant production but rather because of slow decomposition of roots and wood under anaerobic conditions that result from nearly constant high water levels.