Ecosystem Exchange (ecosystem + exchange)

Distribution by Scientific Domains

Kinds of Ecosystem Exchange

  • net ecosystem exchange


  • Selected Abstracts


    Carbon dioxide assimilation by a wetland sedge canopy exposed to ambient and elevated CO2: measurements and model analysis

    FUNCTIONAL ECOLOGY, Issue 2 2003
    D. P. Rasse
    Summary 1The wetland sedge Scirpus olneyi Gray displays fast rates of CO2 assimilation and responds positively to increased atmospheric CO2 concentration. The present study was aimed at identifying the ecophysiological traits specific to S. olneyi that drive these CO2 -assimilation patterns under ambient and elevated CO2 conditions. 2The net ecosystem exchange (NEE) of CO2 between S. olneyi communities and the atmosphere was measured in open-top chambers. 3We developed a new mechanistic model for S. olneyi communities based on published ecophysiological data and additional measurements of photosynthetic parameters. 4Our NEE measurements confirmed that S. olneyi communities have a high rate of summertime CO2 assimilation, with noontime peaks reaching 40 µmol CO2 m,2 ground s,1 on productive summer days, and that elevated CO2 increased S. olneyi CO2 assimilation by c. 35,40%. 5Using S. olneyi -specific ecophysiological parameters, comparison with measured NEE showed that the model accurately simulated these high rates of CO2 uptake under ambient or elevated CO2. 6The model pointed to the Rubisco capacity of Scirpus leaves associated with their high total nitrogen content as the primary explanation for the high rates of CO2 assimilation, and indicated that the vertical-leaf canopy structure of S. olneyi had comparatively little influence on CO2 assimilation. [source]


    Seasonal and annual variation of carbon exchange in an evergreen Mediterranean forest in southern France

    GLOBAL CHANGE BIOLOGY, Issue 4 2008
    V. ALLARD
    Abstract We present 9 years of eddy covariance measurements made over an evergreen Mediterranean forest in southern France. The goal of this study was to quantify the different components of the carbon (C) cycle, gross primary production (GPP) and ecosystem respiration (Reco), and to assess the effects of climatic variables on these fluxes and on the net ecosystem exchange of carbon dioxide. The Puéchabon forest acted as a net C sink of ,254 g C m,2 yr,1, with a GPP of 1275 g C m,2 yr,1 and a Reco of 1021 g C m,2 yr,1. On average, 83% of the net annual C sink occurred between March and June. The effects of exceptional events such the insect-induced partial canopy defoliation that occurred in spring 2005, and the spring droughts of 2005 and 2006 are discussed. A high interannual variability of ecosystem C fluxes during summer and autumn was observed but the resulting effect on the annual net C budget was moderate. Increased severity and/or duration of summer drought under climate change do not appear to have the potential to negatively impact the average C budget of this ecosystem. On the contrary, factors affecting ecosystem functioning (drought and/or defoliation) during March,June period may reduce dramatically the annual C balance of evergreen Mediterranean forests. [source]


    Net regional ecosystem CO2 exchange from airborne and ground-based eddy covariance, land-use maps and weather observations

    GLOBAL CHANGE BIOLOGY, Issue 3 2007
    F. MIGLIETTA
    Abstract Measurements of regional net ecosystem exchange (NEE) were made over a period of 21 days in summer 2002 in the South-Central part of the Netherlands and extrapolated to an area of 13 000 km2 using a combination of flux measurements made by a Sky Arrow ERA research aircraft, half-hourly eddy covariance data from four towers, half-hourly weather data recorded by three weather stations and detailed information on regional land use. The combination of this type of information allowed to estimate the net contribution of the terrestrial ecosystems to the overall regional carbon flux and to map dynamically the temporal and spatial variability of the fluxes. A regional carbon budget was calculated for the study period and the contributions of the different land uses to the overall regional flux, were assessed. Ecosystems were, overall, a small source of carbon to the atmosphere equivalent to to 0.23±0.025 g C m,2 day,1. When considered separately, arable and grasslands were a source of, respectively, 0.68±0.022 and 1.28±0.026 g C m,2 day,1. Evergreen and deciduous forests were instead a sink of ,1.42±0.015 g C m,2 day,1. During the study period, forests offset approximately 3.5% of anthropogenic carbon emission estimates obtained from inventory data. Lacking of a robust validation, NEE values obtained with this method were compared with independent state of art estimates of the regional carbon balance that were obtained by applying a semi-empirical model of NEE driven by MODIS satellite fAPAR data. The comparison showed an acceptable matching for the carbon balance of forest that was a sink in both cases, while a much larger difference for arable and grassland was found. Those ecosystems were a sink for satellite-based estimates while they were a source for the combined aircraft and tower estimates. Possible causes of such differences are discussed and partly addressed. The importance of new methods for determining carbon balance at the regional scale, is outlined. [source]


    Ecophysiological controls over the net ecosystem exchange of mountain spruce stand.

    GLOBAL CHANGE BIOLOGY, Issue 1 2007
    Comparison of the response in direct vs. diffuse solar radiation
    Abstract Cloud cover increases the proportion of diffuse radiation reaching the Earth's surface and affects many microclimatic factors such as temperature, vapour pressure deficit and precipitation. We compared the relative efficiencies of canopy photosynthesis to diffuse and direct photosynthetic photon flux density (PPFD) for a Norway spruce forest (25-year-old, leaf area index 11 m2 m,2) during two successive 7-day periods in August. The comparison was based on the response of net ecosystem exchange (NEE) of CO2 to PPFD. NEE and stomatal conductance at the canopy level (Gcanopy) was estimated from half-hourly eddy-covariance measurements of CO2 and H2O fluxes. In addition, daily courses of CO2 assimilation rate (AN) and stomatal conductance (Gs) at shoot level were measured using a gas-exchange technique applied to branches of trees. The extent of spectral changes in incident solar radiation was assessed using a spectroradiometer. We found significantly higher NEE (up to 150%) during the cloudy periods compared with the sunny periods at corresponding PPFDs. Prevailing diffuse radiation under the cloudy days resulted in a significantly lower compensation irradiance (by ca. 50% and 70%), while apparent quantum yield was slightly higher (by ca. 7%) at canopy level and significantly higher (by ca. 530%) in sun-acclimated shoots. The main reasons for these differences appear to be (1) more favourable microclimatic conditions during cloudy periods, (2) stimulation of photochemical reactions and stomatal opening via an increase of blue/red light ratio, and (3) increased penetration of light into the canopy and thus a more equitable distribution of light between leaves. Our analyses identified the most important reason of enhanced NEE under cloudy sky conditions to be the effective penetration of diffuse radiation to lower depths of the canopy. This subsequently led to the significantly higher solar equivalent leaf area compared with the direct radiation. Most of the leaves in such dense canopy are in deep shade, with marginal or negative carbon balances during sunny days. These findings show that the energy of diffuse, compared with direct, solar radiation is used more efficiently in assimilation processes at both leaf and canopy levels. [source]


    Partitioning sources of soil respiration in boreal black spruce forest using radiocarbon

    GLOBAL CHANGE BIOLOGY, Issue 2 2006
    Edward A.G. Schuur
    Abstract Separating ecosystem and soil respiration into autotrophic and heterotrophic component sources is necessary for understanding how the net ecosystem exchange of carbon (C) will respond to current and future changes in climate and vegetation. Here, we use an isotope mass balance method based on radiocarbon to partition respiration sources in three mature black spruce forest stands in Alaska. Radiocarbon (,14C) signatures of respired C reflect the age of substrate C and can be used to differentiate source pools within ecosystems. Recently-fixed C that fuels plant or microbial metabolism has ,14C values close to that of current atmospheric CO2, while C respired from litter and soil organic matter decomposition will reflect the longer residence time of C in plant and soil C pools. Contrary to our expectations, the ,14C of C respired by recently excised black spruce roots averaged 14, greater than expected for recently fixed photosynthetic products, indicating that some portion of the C fueling root metabolism was derived from C storage pools with turnover times of at least several years. The ,14C values of C respired by heterotrophs in laboratory incubations of soil organic matter averaged 60, higher than the contemporary atmosphere ,14CO2, indicating that the major contributors to decomposition are derived from a combination of sources consistent with a mean residence time of up to a decade. Comparing autotrophic and heterotrophic ,14C end members with measurements of the ,14C of total soil respiration, we calculated that 47,63% of soil CO2 emissions were derived from heterotrophic respiration across all three sites. Our limited temporal sampling also observed no significant differences in the partitioning of soil respiration in the early season compared with the late season. Future work is needed to address the reasons for high ,14C values in root respiration and issues of whether this method fully captures the contribution of rhizosphere respiration. [source]


    Ecohydrological impacts of woody-plant encroachment: seasonal patterns of water and carbon dioxide exchange within a semiarid riparian environment

    GLOBAL CHANGE BIOLOGY, Issue 2 2006
    RUSSELL L. SCOTT
    Abstract Across many dryland regions, historically grass-dominated ecosystems have been encroached upon by woody-plant species. In this paper, we compare ecosystem water and carbon dioxide (CO2) fluxes over a grassland, a grassland,shrubland mosaic, and a fully developed woodland to evaluate potential consequences of woody-plant encroachment on important ecosystem processes. All three sites were located in the riparian corridor of a river in the southwest US. As such, plants in these ecosystems may have access to moisture at the capillary fringe of the near-surface water table. Using fluxes measured by eddy covariance in 2003 we found that ecosystem evapotranspiration (ET) and net ecosystem exchange of carbon dioxide (NEE) increased with increasing woody-plant dominance. Growing season ET totals were 407, 450, and 639 mm in the grassland, shrubland, and woodland, respectively, and in excess of precipitation by 227, 265, and 473 mm. This excess was derived from groundwater, especially during the extremely dry premonsoon period when this was the only source of moisture available to plants. Access to groundwater by the deep-rooted woody plants apparently decouples ecosystem ET from gross ecosystem production (GEP) with respect to precipitation. Compared with grasses, the woody plants were better able to use the stable groundwater source and had an increased net CO2 gain during the dry periods. This enhanced plant activity resulted in substantial accumulation of leaf litter on the soil surface that, during rainy periods, may lead to high microbial respiration rates that offset these photosynthetic fluxes. March,December (primary growing season) totals of NEE were ,63, ,212, and ,233 g C m,2 in the grassland, shrubland, and woodland, respectively. Thus, there was a greater disparity between ecosystem water use and the strength of the CO2 sink as woody plants increased across the encroachment gradient. Despite a higher density of woody plants and a greater plant productivity in the woodland than in the shrubland, the woodland produced a larger respiration response to rainfall that largely offset its higher photosynthetic potential. These data suggest that the capacity for woody plants to exploit water resources in riparian areas results in enhanced carbon sequestration at the expense of increased groundwater use under current climate conditions, but the potential does not scale specifically as a function of woody-plant abundance. These results highlight the important roles of water sources and ecosystem structure on the control of water and carbon balances in dryland areas. [source]


    The conversion of the corn/soybean ecosystem to no-till agriculture may result in a carbon sink

    GLOBAL CHANGE BIOLOGY, Issue 11 2005
    Carl J. Bernacchi
    Abstract Mitigating or slowing an increase in atmospheric carbon dioxide concentration ([CO2]) has been the focus of international efforts, most apparent with the development of the Kyoto Protocol. Sequestration of carbon (C) in agricultural soils is being advocated as a method to assist in meeting the demands of an international C credit system. The conversion of conventionally tilled agricultural lands to no till is widely accepted as having a large-scale sequestration potential. In this study, C flux measurements over a no-till corn/soybean agricultural ecosystem over 6 years were coupled with estimates of C release associated with agricultural practices to assess the net biome productivity (NBP) of this no-till ecosystem. Estimates of NBP were also calculated for the conventionally tilled corn/soybean ecosystem assuming net ecosystem exchange is C neutral. These measurements were scaled to the US as a whole to determine the sequestration potential of corn/soybean ecosystems, under current practices where 10% of agricultural land devoted to this ecosystem is no-tilled and under a hypothetical scenario where 100% of the land is not tilled. The estimates of this analysis show that current corn/soybean agriculture in the US releases ,7.2 Tg C annually, with no-till sequestering ,2.2 Tg and conventional-till releasing ,9.4 Tg. The complete conversion of land area to no till might result in 21.7 Tg C sequestered annually, representing a net C flux difference of ,29 Tg C. These results demonstrate that large-scale conversion to no-till practices, at least for the corn/soybean ecosystem, could potentially offset ca. 2% of annual US carbon emissions. [source]


    Estimating diurnal to annual ecosystem parameters by synthesis of a carbon flux model with eddy covariance net ecosystem exchange observations

    GLOBAL CHANGE BIOLOGY, Issue 2 2005
    Bobby H. Braswell
    Abstract We performed a synthetic analysis of Harvard Forest net ecosystem exchange of CO2 (NEE) time series and a simple ecosystem carbon flux model, the simplified Photosynthesis and Evapo-Transpiration model (SIPNET). SIPNET runs at a half-daily time step, and has two vegetation carbon pools, a single aggregated soil carbon pool, and a simple soil moisture sub-model. We used a stochastic Bayesian parameter estimation technique that provided posterior distributions of the model parameters, conditioned on the observed fluxes and the model equations. In this analysis, we estimated the values of all quantities that govern model behavior, including both rate constants and initial conditions for carbon pools. The purpose of this analysis was not to calibrate the model to make predictions about future fluxes but rather to understand how much information about process controls can be derived directly from the NEE observations. A wavelet decomposition enabled us to assess model performance at multiple time scales from diurnal to decadal. The model parameters are most highly constrained by eddy flux data at daily to seasonal time scales, suggesting that this approach is not useful for calculating annual integrals. However, the ability of the model to fit both the diurnal and seasonal variability patterns in the data simultaneously, using the same parameter set, indicates the effectiveness of this parameter estimation method. Our results quantify the extent to which the eddy covariance data contain information about the ecosystem process parameters represented in the model, and suggest several next steps in model development and observations for improved synthesis of models with flux observations. [source]


    CO2 exchange in three Canadian High Arctic ecosystems: response to long-term experimental warming

    GLOBAL CHANGE BIOLOGY, Issue 12 2004
    Jeffrey M. Welker
    Abstract Carbon dioxide exchange, soil C and N, leaf mineral nutrition and leaf carbon isotope discrimination (LCID-,) were measured in three High Arctic tundra ecosystems over 2 years under ambient and long-term (9 years) warmed (,2°C) conditions. These ecosystems are located at Alexandra Fiord (79°N) on Ellesmere Island, Nunavut, and span a soil water gradient; dry, mesic, and wet tundra. Growing season CO2 fluxes (i.e., net ecosystem exchange (NEE), gross ecosystem photosynthesis (GEP), and ecosystem respiration (Re)) were measured using an infrared gas analyzer and winter C losses were estimated by chemical absorption. All three tundra ecosystems lost CO2 to the atmosphere during the winter, ranging from 7 to 12 g CO2 -C m,2 season,1 being highest in the wet tundra. The period during the growing season when mesic tundra switch from being a CO2 source to a CO2 sink was increased by 2 weeks because of warming and increases in GEP. Warming during the summer stimulated dry tundra GEP more than Re and thus, NEE was consistently greater under warmed as opposed to ambient temperatures. In mesic tundra, warming stimulated GEP with no effect on Re increasing NEE by ,10%, especially in the first half of the summer. During the ,70 days growing season (mid-June,mid-August), the dry and wet tundra ecosystems were net CO2 -C sinks (30 and 67 g C m,2 season,1, respectively) and the mesic ecosystem was a net C source (58 g C m,2 season,1) to the atmosphere under ambient temperature conditions, due in part to unusual glacier melt water flooding that occurred in the mesic tundra. Experimental warming during the growing season increased net C uptake by ,12% in dry tundra, but reduced net C uptake by ,20% in wet tundra primarily because of greater rates of Re as opposed to lower rates of GEP. Mesic tundra responded to long-term warming with ,30% increase in GEP with almost no change in Re reducing this tundra type to a slight C source (17 g C m,2 season,1). Warming caused LCID of Dryas integrafolia plants to be higher in dry tundra and lower in Salix arctic plants in mesic and wet tundra. Our findings indicate that: (1) High Arctic ecosystems, which occur in similar mesoclimates, have different net CO2 exchange rates with the atmosphere; (2) long-term warming can increase the net CO2 exchange of High Arctic tundra by stimulating GEP, but it can also reduce net CO2 exchange in some tundra types during the summer by stimulating Re to a greater degree than stimulating GEP; (3) after 9 years of experimental warming, increases in soil carbon and nitrogen are detectable, in part, because of increases in deciduous shrub cover, biomass, and leaf litter inputs; (4) dry tundra increases in GEP, in response to long-term warming, is reflected in D. integrifolia LCID; and (5) the differential carbon exchange responses of dry, mesic, and wet tundra to similar warming magnitudes appear to depend, in part, on the hydrologic (soil water) conditions. Annual net ecosystem CO2 -C exchange rates ranged from losses of 64 g C m,2 yr,1 to gains of 55 g C m,2 yr,1. These magnitudes of positive NEE are close to the estimates of NPP for these tundra types in Alexandra Fiord and in other High Arctic locations based on destructive harvests. [source]


    Simulated and observed fluxes of sensible and latent heat and CO2 at the WLEF-TV tower using SiB2.5

    GLOBAL CHANGE BIOLOGY, Issue 9 2003
    Ian Baker
    Abstract Three years of meteorological data collected at the WLEF-TV tower were used to drive a revised version of the Simple Biosphere (SiB 2.5) Model. Physiological properties and vegetation phenology were specified from satellite imagery. Simulated fluxes of heat, moisture, and carbon were compared to eddy covariance measurements taken onsite as a means of evaluating model performance on diurnal, synoptic, seasonal, and interannual time scales. The model was very successful in simulating variations of latent heat flux when compared to observations, slightly less so in the simulation of sensible heat flux. The model overestimated peak values of sensible heat flux on both monthly and diurnal scales. There was evidence that the differences between observed and simulated fluxes might be linked to wetlands near the WLEF tower, which were not present in the SiB simulation. The model overestimated the magnitude of the net ecosystem exchange of CO2 in both summer and winter. Mid-day maximum assimilation was well represented by the model, but late afternoon simulations showed excessive carbon uptake due to misrepresentation of within-canopy shading in the model. Interannual variability was not well simulated because only a single year of satellite imagery was used to parameterize the model. [source]


    Evaluation of six process-based forest growth models using eddy-covariance measurements of CO2 and H2O fluxes at six forest sites in Europe

    GLOBAL CHANGE BIOLOGY, Issue 3 2002
    K. Kramer
    Abstract Reliable models are required to assess the impacts of climate change on forest ecosystems. Precise and independent data are essential to assess this accuracy. The flux measurements collected by the EUROFLUX project over a wide range of forest types and climatic regions in Europe allow a critical testing of the process-based models which were developed in the LTEEF project. The ECOCRAFT project complements this with a wealth of independent plant physiological measurements. Thus, it was aimed in this study to test six process-based forest growth models against the flux measurements of six European forest types, taking advantage of a large database with plant physiological parameters. The reliability of both the flux data and parameter values itself was not under discussion in this study. The data provided by the researchers of the EUROFLUX sites, possibly with local corrections, were used with a minor gap-filling procedure to avoid the loss of many days with observations. The model performance is discussed based on their accuracy, generality and realism. Accuracy was evaluated based on the goodness-of-fit with observed values of daily net ecosystem exchange, gross primary production and ecosystem respiration (gC m,2 d,1), and transpiration (kg H2O m,2 d,1). Moreover, accuracy was also evaluated based on systematic and unsystematic errors. Generality was characterized by the applicability of the models to different European forest ecosystems. Reality was evaluated by comparing the modelled and observed responses of gross primary production, ecosystem respiration to radiation and temperature. The results indicated that: Accuracy. All models showed similar high correlation with the measured carbon flux data, and also low systematic and unsystematic prediction errors at one or more sites of flux measurements. The results were similar in the case of several models when the water fluxes were considered. Most models fulfilled the criteria of sufficient accuracy for the ability to predict the carbon and water exchange between forests and the atmosphere. Generality. Three models of six could be applied for both deciduous and coniferous forests. Furthermore, four models were applied both for boreal and temperate conditions. However, no severe water-limited conditions were encountered, and no year-to-year variability could be tested. Realism. Most models fulfil the criterion of realism that the relationships between the modelled phenomena (carbon and water exchange) and environment are described causally. Again several of the models were able to reproduce the responses of measurable variables such as gross primary production (GPP), ecosystem respiration and transpiration to environmental driving factors such as radiation and temperature. Stomatal conductance appears to be the most critical process causing differences in predicted fluxes of carbon and water between those models that accurately describe the annual totals of GPP, ecosystem respiration and transpiration. As a conclusion, several process-based models are available that produce accurate estimates of carbon and water fluxes at several forest sites of Europe. This considerable accuracy fulfils one requirement of models to be able to predict the impacts of climate change on the carbon balance of European forests. However, the generality of the models should be further evaluated by expanding the range of testing over both time and space. In addition, differences in behaviour between models at the process level indicate requirement of further model testing, with special emphasis on modelling stomatal conductance realistically. [source]


    Carbon dioxide exchange of a Russian boreal forest after disturbance by wind throw

    GLOBAL CHANGE BIOLOGY, Issue 3 2002
    Alexander Knohl
    Abstract The exchange of carbon dioxide (CO2) between the atmosphere and a forest after disturbance by wind throw in the western Russian taiga was investigated between July and October 1998 using the eddy covariance technique. The research area was a regenerating forest (400 m × 1000 m), in which all trees of the preceding generation were uplifted during a storm in 1996. All deadwood had remained on site after the storm and had not been extracted for commercial purposes. Because of the heterogeneity of the terrain, several micrometeorological quality tests were applied. In addition to the eddy covariance measurements, carbon pools of decaying wood in a chronosequence of three different wind throw areas were analysed and the decay rate of coarse woody debris was derived. During daytime, the average CO2 uptake flux was ,3 µmol m,2s,1, whereas during night-time characterised by a well-mixed atmosphere the rates of release were typically about 6 µmol m,2s,1. Suppression of turbulent fluxes was only observed under conditions with very low friction velocity (u* , 0.08 ms,1). On average, 164 mmol CO2 m,2d,1 was released from the wind throw to the atmosphere, giving a total of 14.9 mol CO2 m,2 (180 g CO2 m,2) released during the 3-month study period. The chronosequence of dead woody debris on three different wind throw areas suggested exponential decay with a decay coefficient of ,0.04 yr,1. From the magnitude of the carbon pools and the decay rate, it is estimated that the decomposition of coarse woody debris accounted for about a third of the total ecosystem respiration at the measurement site. Hence, coarse woody debris had a long-term influence on the net ecosystem exchange of this wind throw area. From the analysis performed in this work, a conclusion is drawn that it is necessary to include into flux networks the ecosystems that are subject to natural disturbances and that have been widely omitted into considerations of the global carbon budget. The half-life time of about 17 years for deadwood in the wind throw suggests a fairly long storage of carbon in the ecosystem, and indicates a very different long-term carbon budget for naturally disturbed vs. commercially managed forests. [source]


    Modelling night-time ecosystem respiration by a constrained source optimization method

    GLOBAL CHANGE BIOLOGY, Issue 2 2002
    Chun-Ta Lai
    Abstract One of the main challenges to quantifying ecosystem carbon budgets is properly quantifying the magnitude of night-time ecosystem respiration. Inverse Lagrangian dispersion analysis provides a promising approach to addressing such a problem when measured mean CO2 concentration profiles and nocturnal velocity statistics are available. An inverse method, termed ,Constrained Source Optimization' or CSO, which couples a localized near-field theory (LNF) of turbulent dispersion to respiratory sources, is developed to estimate seasonal and annual components of ecosystem respiration. A key advantage to the proposed method is that the effects of variable leaf area density on flow statistics are explicitly resolved via higher-order closure principles. In CSO, the source distribution was computed after optimizing key physiological parameters to recover the measured mean concentration profile in a least-square fashion. The proposed method was field-tested using 1 year of 30-min mean CO2 concentration and CO2 flux measurements collected within a 17-year-old (in 1999) even-aged loblolly pine (Pinus taeda L.) stand in central North Carolina. Eddy-covariance flux measurements conditioned on large friction velocity, leaf-level porometry and forest-floor respiration chamber measurements were used to assess the performance of the CSO model. The CSO approach produced reasonable estimates of ecosystem respiration, which permits estimation of ecosystem gross primary production when combined with daytime net ecosystem exchange (NEE) measurements. We employed the CSO approach in modelling annual respiration of above-ground plant components (c. 214 g C m,2 year,1) and forest floor (c. 989 g C m,2 year,1) for estimating gross primary production (c. 1800 g C m,2 year,1) with a NEE of c. 605 g C m,2 year,1 for this pine forest ecosystem. We conclude that the CSO approach can utilise routine CO2 concentration profile measurements to corroborate forest carbon balance estimates from eddy-covariance NEE and chamber-based component flux measurements. [source]


    Carbon storage and fluxes in ponderosa pine forests at different developmental stages

    GLOBAL CHANGE BIOLOGY, Issue 7 2001
    B.E. Law
    Abstract We compared carbon storage and fluxes in young and old ponderosa pine stands in Oregon, including plant and soil storage, net primary productivity, respiration fluxes, eddy flux estimates of net ecosystem exchange (NEE), and Biome-BGC simulations of fluxes. The young forest (Y site) was previously an old-growth ponderosa pine forest that had been clearcut in 1978, and the old forest (O site), which has never been logged, consists of two primary age classes (50 and 250 years old). Total ecosystem carbon content (vegetation, detritus and soil) of the O forest was about twice that of the Y site (21 vs. 10 kg C m,2 ground), and significantly more of the total is stored in living vegetation at the O site (61% vs. 15%). Ecosystem respiration (Re) was higher at the O site (1014 vs. 835 g C m,2 year,1), and it was largely from soils at both sites (77% of Re). The biological data show that above-ground net primary productivity (ANPP), NPP and net ecosystem production (NEP) were greater at the O site than the Y site. Monte Carlo estimates of NEP show that the young site is a source of CO2 to the atmosphere, and is significantly lower than NEP(O) by c. 100 g C m,2 year,1. Eddy covariance measurements also show that the O site was a stronger sink for CO2 than the Y site. Across a 15-km swath in the region, ANPP ranged from 76 g C m,2 year,1 at the Y site to 236 g C m,2 year,1 (overall mean 158 ± 14 g C m,2 year,1). The lowest ANPP values were for the youngest and oldest stands, but there was a large range of ANPP for mature stands. Carbon, water and nitrogen cycle simulations with the Biome-BGC model suggest that disturbance type and frequency, time since disturbance, age-dependent changes in below-ground allocation, and increasing atmospheric concentration of CO2 all exert significant control on the net ecosystem exchange of carbon at the two sites. Model estimates of major carbon flux components agree with budget-based observations to within ±,20%, with larger differences for NEP and for several storage terms. Simulations showed the period of regrowth required to replace carbon lost during and after a stand-replacing fire (O) or a clearcut (Y) to be between 50 and 100 years. In both cases, simulations showed a shift from net carbon source to net sink (on an annual basis) 10,20 years after disturbance. These results suggest that the net ecosystem production of young stands may be low because heterotrophic respiration, particularly from soils, is higher than the NPP of the regrowth. The amount of carbon stored in long-term pools (biomass and soils) in addition to short-term fluxes has important implications for management of forests in the Pacific North-west for carbon sequestration. [source]


    Leaf age affects the seasonal pattern of photosynthetic capacityand net ecosystem exchange of carbon in a deciduous forest

    PLANT CELL & ENVIRONMENT, Issue 6 2001
    K. B. Wilson
    Abstract Temporal trends in photosynthetic capacity are a critical factorin determining the seasonality and magnitude of ecosystem carbonfluxes. At a mixed deciduous forest in the south-eastern United States (Walker Branch Watershed, Oak Ridge, TN, USA), we independently measured seasonal trends in photosynthetic capacity (using single-leaf gas exchange techniques) and the whole-canopycarbon flux (using the eddy covariance method). Soil respiration was also measured using chambers and an eddy covariance system beneath the canopy. These independent chamber and eddy covariance measurements, along with a biophysical model (CANOAK), areused to examine how leaf age affects the seasonal pattern of carbon uptake during the growing season. When the measured seasonality in photosynthetic capacity is representedin the CANOAK simulations, there is good agreement with the eddy covariance data on the seasonal trends in carbon uptake. Removing the temporal trends in the simulations by using the early season maximum value of photosynthetic capacity over the entire growing season over estimates the annual carbon uptake by about 300 g C m,2 year,1, halfthe total estimated annual net ecosystem exchange. Alternatively, use of the mean value of photosynthetic capacity incorrectly simulates the seasonality in carbon uptake by the forest. In addition to changes related to leaf development and senescence, photosynthetic capacitydecreased in the middle and late summer, even when leaf nitrogenwas essentially constant. When only these middle and late summer reductions were neglected in the model simulations, CANOAK still overestimated the carbon uptake by an amount comparable to 25% ofthe total annual net ecosystem exchange. [source]