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1.
Carbon balance of different aged Scots pine forests in Southern Finland   总被引:4,自引:0,他引:4  
We estimated annual net ecosystem exchange (NEE) of a chronosequence of four Scots pine stands in southern Finland during years 2000–2002 using eddy covariance (EC). Net ecosystem productivity (NEP) was estimated using growth measurements and modelled mass losses of woody debris. The stands were 4, 12, 40 and 75 years old. The 4‐year‐old clearcut was a source of carbon throughout the year combining a low gross primary productivity (GPP) with a total ecosystem respiration (TER) similar to the forest stands. The annual NEE of the clearcut, measured by EC, was 386 g C m?2. Tree growth was negligible and the estimated NEP was ?262 g C m?2 a?1. The annual GPPs at the other sites were close to each other (928?1072 g C m?2 a?1), but TER differed markedly, being greatest at the 12‐year‐old site (905 g C m?2 a?1) and smallest in the 75‐year‐old stand (616 g C m?2 a?1). Measurements of soil CO2 efflux showed that different rates of soil respiration largely explained the differences in TER. The NEE and NEP of the 12‐year‐old stand were close to zero. The forested stands were sinks of carbon. They had similar annual patterns of carbon exchange and half‐hourly eddy fluxes were highly correlated, indicating similar responses to the environment. The NEE in the 40‐year‐old stand varied between ?179 and –192 g C m?2 a?1, while NEP was between 214 and 242 g C m?2 a?1. The annual NEE of the 75‐year‐old stand was 323 g C m?2 and NEP was 252 g C m?2. This indicates that there was no reduction in carbon sink strength with stand age.  相似文献   

2.
Arid ecosystems, which occupy about 35% of the Earth's terrestrial surface area, are believed to be among the most responsive to elevated [CO2]. Net ecosystem CO2 exchange (NEE) was measured in the eighth year of CO2 enrichment at the Nevada Desert Free‐Air CO2 Enrichment (FACE) Facility between the months of December 2003–December 2004. On most dates mean daily NEE (24 h) (μmol CO2 m?2 s?1) of ecosystems exposed to elevated atmospheric CO2 were similar to those maintained at current ambient CO2 levels. However, on sampling dates following rains, mean daily NEEs of ecosystems exposed to elevated [CO2] averaged 23 to 56% lower than mean daily NEEs of ecosystems maintained at ambient [CO2]. Mean daily NEE varied seasonally across both CO2 treatments, increasing from about 0.1 μmol CO2 m?2 s?1 in December to a maximum of 0.5–0.6 μmol CO2 m?2 s?1 in early spring. Maximum NEE in ecosystems exposed to elevated CO2 occurred 1 month earlier than it did in ecosystems exposed to ambient CO2, with declines in both treatments to lowest seasonal levels by early October (0.09±0.03 μmol CO2 m?2 s?1), but then increasing to near peak levels in late October (0.36±0.08 μmol CO2 m?2 s?1), November (0.28±0.03 μmol CO2 m?2 s?1), and December (0.54±0.06 μmol CO2 m?2 s?1). Seasonal patterns of mean daily NEE primarily resulted from larger seasonal fluctuations in rates of daytime net ecosystem CO2 uptake which were closely tied to plant community phenology and precipitation. Photosynthesis in the autotrophic crust community (lichens, mosses, and free‐living cyanobacteria) following rains were probably responsible for the high NEEs observed in January, February, and late October 2004 when vascular plant photosynthesis was low. Both CO2 treatments were net CO2 sinks in 2004, but exposure to elevated CO2 reduced CO2 sink strength by 30% (positive net ecosystem productivity=127±17 g C m?2 yr?1 ambient CO2 and 90±11 g C m?2 yr?1 elevated CO2, P=0.011). This level of net C uptake rivals or exceeds levels observed in some forested and grassland ecosystems. Thus, the decrease in C sequestration seen in our study under elevated CO2– along with the extensive coverage of arid and semi‐arid ecosystems globally – points to a significant drop in global C sequestration potential in the next several decades because of responses of heretofore overlooked dryland ecosystems.  相似文献   

3.
Energy derived from second generation perennial energy crops is projected to play an increasingly important role in the decarbonization of the energy sector. Such energy crops are expected to deliver net greenhouse gas emissions reductions through fossil fuel displacement and have potential for increasing soil carbon (C) storage. Despite this, few empirical studies have quantified the ecosystem‐level C balance of energy crops and the evidence base to inform energy policy remains limited. Here, the temporal dynamics and magnitude of net ecosystem carbon dioxide (CO2) exchange (NEE) were quantified at a mature short rotation coppice (SRC) willow plantation in Lincolnshire, United Kingdom, under commercial growing conditions. Eddy covariance flux observations of NEE were performed over a four‐year production cycle and combined with biomass yield data to estimate the net ecosystem carbon balance (NECB) of the SRC. The magnitude of annual NEE ranged from ?147 ± 70 to ?502 ± 84 g CO2‐C m?2 year?1 with the magnitude of annual CO2 capture increasing over the production cycle. Defoliation during an unexpected outbreak of willow leaf beetle impacted gross ecosystem production, ecosystem respiration, and net ecosystem exchange during the second growth season. The NECB was ?87 ± 303 g CO2‐C m?2 for the complete production cycle after accounting for C export at harvest (1,183 g C m?2), and was approximately CO2‐C neutral (?21 g CO2‐C m?2 year?1) when annualized. The results of this study are consistent with studies of soil organic C which have shown limited changes following conversion to SRC willow. In the context of global decarbonization, the study indicates that the primary benefit of SRC willow production at the site is through displacement of fossil fuel emissions.  相似文献   

4.
We used eddy covariance and biomass measurements to quantify the carbon (C) dynamics of a naturally regenerated longleaf pine/slash pine flatwoods ecosystem in north Florida for 4 years, July 2000 to June 2002 and 2004 to 2005, to quantify how forest type, silvicultural intensity and environment influence stand‐level C balance. Precipitation over the study periods ranged from extreme drought (July 2000–June 2002) to above‐average precipitation (2004 and 2005). After photosynthetic photon flux density (PPFD), vapor pressure deficit (VPD) >1.5 kPa and air temperature <10 °C were important constraints on daytime half‐hourly net CO2 exchange (NEEday) and reduced the magnitude of midday CO2 exchange by >5 μmol CO2 m?2 s?1. Analysis of water use efficiency indicated that stomatal closure at VPD>1.5 kPa moderated transpiration similarly in both drought and wet years. Night‐time exchange (NEEnight) was an exponential function of air temperature, with rates further modulated by soil moisture. Estimated annual net ecosystem production (NEP) was remarkably consistent among the four measurement years (range: 158–192 g C m?2 yr?1). In comparison, annual ecosystem C assimilation estimates from biomass measurements between 2000 and 2002 ranged from 77 to 136 g C m?2 yr?1. Understory fluxes accounted for approximately 25–35% of above‐canopy NEE over 24‐h periods, and 85% and 27% of whole‐ecosystem fluxes during night and midday (11:00–15:00 hours) periods, respectively. Concurrent measurements of a nearby intensively managed slash pine plantation showed that annual NEP was three to four times greater than that of the Austin Cary Memorial Forest, highlighting the importance of silviculture and management in regulating stand‐level C budgets.  相似文献   

5.
Difficulty in balancing the global carbon budget has lead to increased attention on tropical forests, which have been estimated to account for up to one third of global gross primary production. Whether tropical forests are sources, sinks, or neutral with respect to their carbon balance with the atmosphere remains unclear. To address this issue, estimates of net ecosystem exchange of carbon (NEE) were made for 3 years (1998–2000) using the eddy‐covariance technique in a tropical wet forest in Costa Rica. Measurements were made from a 42 m tower centred in an old‐growth forest. Under unstable conditions, the measurement height was at least twice the estimated zeroplane height from the ground. The canopy at the site is extremely rough; under unstable conditions the median aerodynamic roughness length ranged from 2.4 to 3.6 m. No relationship between NEE and friction velocity (u*) was found using all of the 30‐min averages. However, there was a linear relationship between the nighttime NEE and averaged u* (R2 = 0.98). The diurnal pattern of flux was similar to that found in other tropical forests, with mean daytime NEE ca. ? 18 μ mol CO2 m?2 s?1 and mean nighttime NEE 4.6 μ mol CO2 m?2 s?1. However, because ~ 80% of the nighttime data in this forest were collected during low u* conditions ( < 0.2 m s?1), nighttime NEE was likely underestimated. Using an alternative analysis, mean nighttime NEE increased to 7.05 μ mol CO2 m?2 s?1. There were interannual differences in NEE, but seasonal differences were not apparent. Irradiance accounted for ~ 51% of the variation in the daytime fluxes, with temperature and vapour pressure deficit together accounting for another ~ 20%. Light compensation points ranged from 100 to 207 μ mol PPFD m?2 s?1. No was relationship was found between 30‐min nighttime NEE and tower‐top air temperature. A weak relationship was found between hourly nighttime NEE and canopy air temperature using data averaged hourly over the entire sampling period (Q10 = 1.79, R2 = 0.17). The contribution of below‐sensor storage was fairly constant from day to day. Our data indicate that this forest was a slight carbon source in 1998 (0.05 to ?1.33 t C ha?1 yr?1), a moderate sink in 1999 (?1.53 to ?3.14 t C ha?1 yr?1), and a strong sink in 2000 (?5.97 to ?7.92 t C ha?1 yr?1). This trend is interpreted as relating to the dissipation of warm‐phase El Niño effects over the course of this study.  相似文献   

6.
Eddy covariance was used to measure the net CO2 exchange (NEE) over ecosystems differing in land use (forest and agriculture) in Thuringia, Germany. Measurements were carried out at a managed, even‐aged European beech stand (Fagus sylvatica, 70–150 years old), an unmanaged, uneven‐aged mixed beech stand in a late stage of development (F. sylvatica, Fraxinus excelsior, Acer pseudoplantanus, and other hardwood trees, 0–250 years old), a managed young Norway spruce stand (Picea abies, 50 years old), and an agricultural field growing winter wheat in 2001, and potato in 2002. Large contrasts were found in NEE rates between the land uses of the ecosystems. The managed and unmanaged beech sites had very similar net CO2 uptake rates (~?480 to ?500 g C m?2 yr?1). Main differences in seasonal NEE patterns between the beech sites were because of a later leaf emergence and higher maximum leaf area index at the unmanaged beech site, probably as a result of the species mix at the site. In contrast, the spruce stand had a higher CO2 uptake in spring but substantially lower net CO2 uptake in summer than the beech stands. This resulted in a near neutral annual NEE (?4 g C m?2 yr?1), mainly attributable to an ecosystem respiration rate almost twice as high as that of the beech stands, despite slightly lower temperatures, because of the higher elevation. Crops in the agricultural field had high CO2 uptake rates, but growing season length was short compared with the forest ecosystems. Therefore, the agricultural land had low‐to‐moderate annual net CO2 uptake (?34 to ?193 g C m?2), but with annual harvest taken into account it will be a source of CO2 (+97 to +386 g C m?2). The annually changing patchwork of crops will have strong consequences on the regions' seasonal and annual carbon exchange. Thus, not only land use, but also land‐use history and site‐specific management decisions affect the large‐scale carbon balance.  相似文献   

7.
Vegetation plays a central role in controlling terrestrial carbon (C) exchange, but quantifying its impacts on C cycling on time scales of ecological succession is hindered by a lack of long‐term observations. The net ecosystem exchange of carbon (NEE) was measured for several years in adjacent ecosystems that represent distinct phases of ecological succession in the southeastern USA. The experiment was designed to isolate the role of vegetation – apart from climate and soils – in controlling biosphere–atmosphere fluxes of CO2 and water vapor. NEE was near zero over 5 years at an early successional old‐field ecosystem (OF). However, mean annual NEE was nearly equal, approximately ?450 g C m?2 yr?1, at an early successional planted pine forest (PP) and a late successional hardwood forest (HW) due to the sensitivity of the former to drought and ice storm damage. We hypothesize that these observations can be explained by the relationships between gross ecosystem productivity (GEP), ecosystem respiration (RE) and canopy conductance, and long‐term shifts in ecosystem physiology in response to climate to maintain near‐constant ecosystem‐level water‐use efficiency (EWUE). Data support our hypotheses, but future research should examine if GEP and RE are causally related or merely controlled by similar drivers. At successional time scales, GEP and RE observations generally followed predictions from E. P. Odum's ‘Strategy of Ecosystem Development’, with the surprising exception that the relationship between GEP and RE resulted in large NEE at the late successional HW. A practical consequence of this research suggests that plantation forestry may confer no net benefit over the conservation of mature forests for C sequestration.  相似文献   

8.
Thus far, grassland ecosystem research has mainly been focused on low‐lying grassland areas, whereas research on high‐altitude grassland areas, especially on the carbon budget of remote areas like the Qinghai‐Tibetan plateau is insufficient. To address this issue, flux of CO2 were measured over an alpine shrubland ecosystem (37°36′N, 101°18′E; 325 above sea level [a. s. l.]) on the Qinghai‐Tibetan Plateau, China, for 2 years (2003 and 2004) with the eddy covariance method. The vegetation is dominated by formation Potentilla fruticosa L. The soil is Mol–Cryic Cambisols. To interpret the biotic and abiotic factors that modulate CO2 flux over the course of a year we decomposed net ecosystem CO2 exchange (NEE) into its constituent components, and ecosystem respiration (Reco). Results showed that seasonal trends of annual total biomass and NEE followed closely the change in leaf area index. Integrated NEE were ?58.5 and ?75.5 g C m?2, respectively, for the 2003 and 2004 years. Carbon uptake was mainly attributed from June, July, August, and September of the growing season. In July, NEE reached seasonal peaks of similar magnitude (4–5 g C m?2 day?1) each of the 2 years. Also, the integrated night‐time NEE reached comparable peak values (1.5–2 g C m?2 day?1) in the 2 years of study. Despite the large difference in time between carbon uptake and release (carbon uptake time < release time), the alpine shrubland was carbon sink. This is probably because the ecosystem respiration at our site was confined significantly by low temperature and small biomass and large day/night temperature difference and usually soil moisture was not limiting factor for carbon uptake. In general, Reco was an exponential function of soil temperature, but with season‐dependent values of Q10. The temperature‐dependent respiration model failed immediately after rain events, when large pulses of Reco were observed. Thus, for this alpine shrubland in Qinghai‐Tibetan plateau, the timing of rain events had more impact than the total amount of precipitation on ecosystem Reco and NEE.  相似文献   

9.
The focus of this study is the relationship between water table depth (WTD) and water vapor [evapotranspiration (ET)] and carbon dioxide [CO2; net ecosystem exchange (NEE)] fluxes in a fen in western Canada. We analyzed hydrological and eddy covariance measurements from four snow‐free periods (2003–2006) with contrasting meteorological conditions to establish the link between daily WTD and ET and gross ecosystem CO2 exchange (GEE) and ecosystem respiration (Reco; NEE=Reco?GEE), respectively: 2003 was warm and dry, 2004 was cool and wet, and 2005 and 2006 were both wet. In 2003, the water table (WT) was below the ground surface. In 2004, the WT rose above the ground surface, and in 2005 and 2006, the WT stayed well above the ground surface. There were no significant differences in total ET (~316 mm period?1), but total NEE was significantly different (2003: 8 g C m?2 period?1; 2004: ?139 g C m?2 period?1; 2005: ?163 g C m?2 period?1; 2006: ?195 g C m?2 period?1), mostly due to differences in total GEE (2003: 327 g C m?2 period?1; 2004: 513 g C m?2 period?1; 2005: 411 g C m?2 period?1; 2006: 556 g C m?2 period?1). Variation in ET is mostly explained by radiation (67%), and the contribution of WTD is only minor (33%). WTD controls the compensating contributions of different land surface components, resulting in similar total ET regardless of the hydrological conditions. WTD and temperature each contribute about half to the explained variation in GEE up to a threshold ponding depth, below which temperature alone is the key explanatory variable. WTD is only of minor importance for the variation in Reco, which is mainly controlled by temperature. Our study implies that future peatland modeling efforts explicitly consider topographic and hydrogeological influences on WTD.  相似文献   

10.
This study reports the annual carbon balance of a drained riparian fen under two‐cut or three‐cut managements of festulolium and tall fescue. CO2 fluxes measured with closed chambers were partitioned into gross primary production (GPP) and ecosystem respiration (ER) for modelling according to environmental factors (light and temperature) and canopy reflectance (ratio vegetation index, RVI). Methodological assessments were made of (i) GPP models with or without temperature functions (Ft) to adjust GPP constraints imposed by low temperature (<10 °C) and (ii) ER models with RVI or GPP parameters as biomass proxies. The sensitivity of the models was also tested on partial datasets including only alternate measurement campaigns and on datasets only from the crop growing period. Use of Ft in GPP models effectively corrected GPP overestimation in cold periods, and this approach was used throughout. Annual fluxes obtained with ER models including RVI or GPP parameters were similar, and also annual GPP and ER fluxes obtained with full and partial datasets were similar. Annual CO2 fluxes and biomass yield were not significantly different in the crop/management combinations although the individual collars (n = 12) showed some variations in GPP (?1818 to ?2409 g CO2‐C m?2), ER (1071 to 1738 g CO2‐C m?2), net ecosystem exchange (NEE, ?669 to ?949 g CO2‐C m?2) and biomass yield (556 to 1044 g CO2‐C m?2). Net ecosystem carbon balance (NECB), as the sum of NEE and biomass carbon export, was only slightly negative to positive in all crop/management combinations. NECBs, interpreted as emission factors, tended to favour the least biomass producing systems as the best management options in relation to climate saving carbon balances. Yet, considering the down‐stream advantages of biomass for fossil fuel replacement, yield‐scaled carbon fluxes are suggested to be given additional considerations for comparison of management options in terms of atmospheric impact.  相似文献   

11.
Radon‐222 (Rn‐222) is used as a transport tracer of forest canopy–atmosphere CO2 exchange in an old‐growth, tropical rain forest site near km 67 of the Tapajós National Forest, Pará, Brazil. Initial results, from month‐long periods at the end of the wet season (June–July) and the end of the dry season (November–December) in 2001, demonstrate the potential of new Rn measurement instruments and methods to quantify mass transport processes between forest canopies and the atmosphere. Gas exchange rates yield mean canopy air residence times ranging from minutes during turbulent daytime hours to greater than 12 h during calm nights. Rn is an effective tracer for net ecosystem exchange of CO2 (CO2 NEE) during calm, night‐time hours when eddy covariance‐based NEE measurements are less certain because of low atmospheric turbulence. Rn‐derived night‐time CO2 NEE (9.00±0.99 μmol m?2 s?1 in the wet season, 6.39±0.59 in the dry season) was significantly higher than raw uncorrected, eddy covariance‐derived CO2 NEE (5.96±0.51 wet season, 5.57±0.53 dry season), but agrees with corrected eddy covariance results (8.65±1.07 wet season, 6.56±0.73 dry season) derived by filtering out lower NEE values obtained during calm periods using independent meteorological criteria. The Rn CO2 results suggest that uncorrected eddy covariance values underestimate night‐time CO2 loss at this site. If generalizable to other sites, these observations indicate that previous reports of strong net CO2 uptake in Amazonian terra firme forest may be overestimated.  相似文献   

12.
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.  相似文献   

13.
Diagnostic carbon cycle models produce estimates of net ecosystem production (NEP, the balance of net primary production and heterotrophic respiration) by integrating information from (i) satellite‐based observations of land surface vegetation characteristics; (ii) distributed meteorological data; and (iii) eddy covariance flux tower observations of net ecosystem exchange (NEE) (used in model parameterization). However, a full bottom‐up accounting of NEE (the vertical carbon flux) that is suitable for integration with atmosphere‐based inversion modeling also includes emissions from decomposition/respiration of harvested forest and agricultural products, CO2 evasion from streams and rivers, and biomass burning. Here, we produce a daily time step NEE for North America for the year 2004 that includes NEP as well as the additional emissions. This NEE product was run in the forward mode through the CarbonTracker inversion setup to evaluate its consistency with CO2 concentration observations. The year 2004 was climatologically favorable for NEP over North America and the continental total was estimated at 1730 ± 370 TgC yr?1 (a carbon sink). Harvested product emissions (316 ± 80 TgC yr?1), river/stream evasion (158 ± 50 TgC yr?1), and fire emissions (142 ± 45 TgC yr?1) counteracted a large proportion (35%) of the NEP sink. Geographic areas with strong carbon sinks included Midwest US croplands, and forested regions of the Northeast, Southeast, and Pacific Northwest. The forward mode run with CarbonTracker produced good agreement between observed and simulated wintertime CO2 concentrations aggregated over eight measurement sites around North America, but overestimates of summertime concentrations that suggested an underestimation of summertime carbon uptake. As terrestrial NEP is the dominant offset to fossil fuel emission over North America, a good understanding of its spatial and temporal variation – as well as the fate of the carbon it sequesters ─ is needed for a comprehensive view of the carbon cycle.  相似文献   

14.
Based on review and original data, this synthesis investigates carbon pools and fluxes of Siberian and European forests (600 and 300 million ha, respectively). We examine the productivity of ecosystems, expressed as positive rate when the amount of carbon in the ecosystem increases, while (following micrometeorological convention) downward fluxes from the atmosphere to the vegetation (NEE = Net Ecosystem Exchange) are expressed as negative numbers. Productivity parameters are Net Primary Productivity (NPP=whole plant growth), Net Ecosystem Productivity (NEP = CO2 assimilation minus ecosystem respiration), and Net Biome Productivity (NBP = NEP minus carbon losses through disturbances bypassing respiration, e.g. by fire and logging). Based on chronosequence studies and national forestry statistics we estimate a low average NPP for boreal forests in Siberia: 123 gC m–2 y–1. This contrasts with a similar calculation for Europe which suggests a much higher average NPP of 460 gC m–2 y–1 for the forests there. Despite a smaller area, European forests have a higher total NPP than Siberia (1.2–1.6 vs. 0.6–0.9 × 1015 gC region–1 y–1). This arises as a consequence of differences in growing season length, climate and nutrition. For a chronosequence of Pinus sylvestris stands studied in central Siberia during summer, NEE was most negative in a 67-y old stand regenerating after fire (– 192 mmol m–2 d–1) which is close to NEE in a cultivated forest of Germany (– 210 mmol m–2 d–1). Considerable net ecosystem CO2-uptake was also measured in Siberia in 200- and 215-y old stands (NEE:174 and – 63 mmol m–2 d–1) while NEP of 7- and 13-y old logging areas were close to the ecosystem compensation point. Two Siberian bogs and a bog in European Russia were also significant carbon sinks (– 102 to – 104 mmol m–2 d–1). Integrated over a growing season (June to September) we measured a total growing season NEE of – 14 mol m–2 summer–1 (– 168 gC m–2 summer–1) in a 200-y Siberian pine stand and – 5 mol m–2 summer–1 (– 60 gC m–2 summer–1) in Siberian and European Russian bogs. By contrast, over the same period, a spruce forest in European Russia was a carbon source to the atmosphere of (NEE: + 7 mol m–2 summer–1 = + 84 gC m–2 summer–1). Two years after a windthrow in European Russia, with all trees being uplifted and few successional species, lost 16 mol C m–2 to the atmosphere over a 3-month in summer, compared to the cumulative NEE over a growing season in a German forest of – 15.5 mol m–2 summer–1 (– 186 gC m–2 summer–1; European flux network annual averaged – 205 gC m–2 y–1). Differences in CO2-exchange rates coincided with differences in the Bowen ratio, with logging areas partitioning most incoming radiation into sensible heat whereas bogs partitioned most into evaporation (latent heat). Effects of these different surface energy exchanges on local climate (convective storms and fires) and comparisons with the Canadian BOREAS experiment are discussed. Following a classification of disturbances and their effects on ecosystem carbon balances, fire and logging are discussed as the main processes causing carbon losses that bypass heterotrophic respiration in Siberia. Following two approaches, NBP was estimated to be only about 13–16 mmol m–2 y–1 for Siberia. It may reach 67 mmol m–2 y–1 in North America, and about 140–400 mmol m–2 y–1 in Scandinavia. We conclude that fire speeds up the carbon cycle, but that it results also in long-term carbon sequestration by charcoal formation. For at least 14 years after logging, regrowth forests remain net sources of CO2 to the atmosphere. This has important implications regarding the effects of Siberian forest management on atmospheric concentrations. For many years after logging has taken place, regrowth forests remain weaker sinks for atmospheric CO2 than are nearby old-growth forests.  相似文献   

15.
To investigate the consequences of land use on carbon and energy exchanges between the ecosystem and atmosphere, we measured CO2 and water vapour fluxes over an introduced Brachiara brizantha pasture located in the Cerrado region of Central Brazil. Measurements using eddy covariance technique were carried out in field campaigns during the wet and dry seasons. Midday CO2 net ecosystem exchange rates during the wet season were ?40 μmol m?2 s?1, which is more than twice the rate found in the dry season (?15 μmol m?2 s?1). This was observed despite similar magnitudes of irradiance, air and soil temperatures. During the wet season, inferred rates of canopy photosynthesis did not show any tendency to saturate at high solar radiation levels, with rates of around 50 μmol m?2 s?1 being observed at the maximum incoming photon flux densities of 2200 μmol m?2 s?1. This contrasted strongly to the dry period when light saturation occurred with 1500 μmol m?2 s?1 and with maximum canopy photosynthetic rates of only 20 μmol m?2 s?1. Both canopy photosynthetic rates and night‐time ecosystem CO2 efflux rates were much greater than has been observed for cerrado native vegetation in both the wet and dry seasons. Indeed, observed CO2 exchange rates were also much greater than has previously been reported for C4 pastures in the tropics. The high rates in the wet season may have been attributable, at least in part, to the pasture not being grazed. Higher than expected net rates of carbon acquisition during the dry season may also have been attributable to some early rain events. Nevertheless, the present study demonstrates that well‐managed, productive tropical pastures can attain ecosystem gas exchange rates equivalent to fertilized C4 crops growing in the temperate zone.  相似文献   

16.
Prater MR  Obrist D  Arnone JA  DeLucia EH 《Oecologia》2006,146(4):595-607
Invasion of non-native annuals across the Intermountain West is causing a widespread transition from perennial sagebrush communities to fire-prone annual herbaceous communities and grasslands. To determine how this invasion affects ecosystem function, carbon and water fluxes were quantified in three, paired sagebrush and adjacent postfire communities in the northern Great Basin using a 1-m3 gas exchange chamber. Most of the plant cover in the postfire communities was invasive species including Bromus tectorum L., Agropyron cristatum (L.) Gaertn and Sisymbrium altissimum L. Instantaneous morning net carbon exchange (NCE) and evapotranspiration (ET) in native shrub plots were greater than either intershrub or postfire plots. Native sagebrush communities were net carbon sinks (mean NCE 0.2–4.3 μmol m−2 s−1) throughout the growing season. The magnitude and seasonal variation of NCE in the postfire communities were controlled by the dominant species and availability of soil moisture. Net C exchange in postfire communities dominated by perennial bunchgrasses was similar to sagebrush. However, communities dominated by annuals (cheatgrass and mustard) had significantly lower NCE than sagebrush and became net sources of carbon to the atmosphere (NCE declined to −0.5 μmol m−2 s−1) with increased severity of the summer drought. Differences in the patterns of ET led to lower surface soil moisture content and increased soil temperatures during summer in the cheatgrass-dominated community compared to the adjacent sagebrush community. Intensive measurements at one site revealed that temporal and spatial patterns of NCE and ET were correlated most closely with changes in leaf area in each community. By altering the patterns of carbon and water exchange, conversion of native sagebrush to postfire invasive communities may disrupt surface-atmosphere exchange and degrade the carbon storage capacity of these systems.  相似文献   

17.
Global modeling efforts indicate semiarid regions dominate the increasing trend and interannual variation of net CO2 exchange with the atmosphere, mainly driven by water availability. Many semiarid regions are expected to undergo climatic drying, but the impacts on net CO2 exchange are poorly understood due to limited semiarid flux observations. Here we evaluated 121 site‐years of annual eddy covariance measurements of net and gross CO2 exchange (photosynthesis and respiration), precipitation, and evapotranspiration (ET) in 21 semiarid North American ecosystems with an observed range of 100 – 1000 mm in annual precipitation and records of 4–9 years each. In addition to evaluating spatial relationships among CO2 and water fluxes across sites, we separately quantified site‐level temporal relationships, representing sensitivity to interannual variation. Across the climatic and ecological gradient, photosynthesis showed a saturating spatial relationship to precipitation, whereas the photosynthesis–ET relationship was linear, suggesting ET was a better proxy for water available to drive CO2 exchanges after hydrologic losses. Both photosynthesis and respiration showed similar site‐level sensitivity to interannual changes in ET among the 21 ecosystems. Furthermore, these temporal relationships were not different from the spatial relationships of long‐term mean CO2 exchanges with climatic ET. Consequently, a hypothetical 100‐mm change in ET, whether short term or long term, was predicted to alter net ecosystem production (NEP) by 64 gCm?2 yr?1. Most of the unexplained NEP variability was related to persistent, site‐specific function, suggesting prioritization of research on slow‐changing controls. Common temporal and spatial sensitivity to water availability increases our confidence that site‐level responses to interannual weather can be extrapolated for prediction of CO2 exchanges over decadal and longer timescales relevant to societal response to climate change.  相似文献   

18.
Invasive insects impact forest carbon dynamics   总被引:3,自引:0,他引:3  
Invasive insects can impact ecosystem functioning by altering carbon, nutrient, and hydrologic cycles. In this study, we used eddy covariance to measure net CO2 exchange with the atmosphere (NEE), and biometric measurements to characterize net ecosystem productivity (NEP) in oak‐ and pine‐dominated forests that were defoliated by Gypsy moth (Lymantria dispar L.) in the New Jersey Pine Barrens. Three years of data were used to compare C dynamics; 2005 with minimal defoliation, 2006 with partial defoliation of the canopy and understory in a mixed stand, and 2007 with complete defoliation of an oak‐dominated stand, and partial defoliation of the mixed and pine‐dominated stands. Previous to defoliation in 2005, annual net CO2 exchange (NEEyr) was estimated at ?187, ?137 and ?204 g C m?2 yr?1 at the oak‐, mixed‐, and pine‐dominated stands, respectively. Annual NEP estimated from biometric measurements was 108%, 100%, and 98% of NEEyr in 2005 for the oak‐, mixed‐, and pine‐dominated stands, respectively. Gypsy moth defoliation strongly reduced fluxes in 2006 and 2007 compared with 2005; NEEyr was ?122, +103, and ?161 g C m?2 yr?1 in 2006, and +293, +129, and ?17 g C m?2 yr?1 in 2007 at the oak‐, mixed‐, and pine‐dominated stands, respectively. At the landscape scale, Gypsy moths defoliated 20.2% of upland forests in 2007. We calculated that defoliation in these upland forests reduced NEEyr by 41%, with a 55% reduction in the heavily impacted oak‐dominated stands. ‘Transient’ disturbances such as insect defoliation, nonstand replacing wildfires, and prescribed burns are major factors controlling NEE across this landscape, and when integrated over time, may explain much of the patterning of aboveground biomass and forest floor mass in these upland forests.  相似文献   

19.
Simultaneous measurements of net ecosystem CO2 exchange (NEE) were made in a Florida scrub‐oak ecosystem in August 1997 and then every month between April 2000 to July 2001, using open top chambers (NEEO) and eddy covariance (NEEE). This study provided a cross validation of these two different techniques for measuring NEE. Unique characteristics of the comparison were that the measurements were made simultaneously, in the same stand, with large replicated chambers enclosing a representative portion of the ecosystem (75 m2, compared to approximately 1–2 ha measured by the eddy covariance system). The value of the comparison was greatest at night, when the microclimate was minimally affected by the chambers. For six of the 12 measurement periods, night NEEO was not significantly different to night NEEE, and for the other periods the maximum difference was 1.1 µ mol m ? 2s ? 1, with an average of 0.72 ± 0.09 µ mol m ? 2s ? 1. The comparison was more difficult during the photoperiod, because of differences between the microclimate inside and outside the chambers. During the photoperiod, air temperature (Tair) and air vapour pressure deficits (VPD) became progressively higher inside the chambers until mid‐afternoon. In the morning NEEO was higher than NEEE by about 26%, consistent with increased temperature inside the chambers. Over the mid‐day period and the afternoon, NEEO was 8% higher that NEEE, regardless of the large differences in microclimate. This study demonstrates both the uses and difficulties associated with attempting to cross validate NEE measurements made in chambers and using eddy covariance. The exercise was most useful at night when the chamber had a minimal effect on microclimate, and when the measurement of NEE is most difficult.  相似文献   

20.
Understanding carbon dynamics of switchgrass ecosystems is crucial as switchgrass (Panicum virgatum L.) acreage is expanding for cellulosic biofuels. We used eddy covariance system and examined seasonal changes in net ecosystem CO2 exchange (NEE) and its components – gross ecosystem photosynthesis (GEP) and ecosystem respiration (ER) – in response to controlling factors during the second (2011) and third (2012) years of stand establishment in the southern Great Plains of the United States (Chickasha, OK). Larger vapor pressure deficit (VPD > 3 kPa) limited photosynthesis and caused asymmetrical diurnal NEE cycles (substantially higher NEE in the morning hours than in the afternoon at equal light levels). Consequently, rectangular hyperbolic light–response curve (NEE partitioning algorithm) consistently failed to provide good fits at high VPD. Modified rectangular hyperbolic light–VPD response model accounted for the limitation of VPD on photosynthesis and improved the model performance significantly. The maximum monthly average NEE reached up to ?33.02 ± 1.96 μmol CO2 m?2 s?1 and the highest daily integrated NEE was ?35.89 g CO2 m?2 during peak growth. Although large differences in cumulative seasonal GEP and ER were observed between two seasons, total seasonal ER accounted for about 75% of GEP regardless of the growing season lengths and differences in aboveground biomass production. It suggests that net ecosystem carbon uptake increases with increasing GEP. The ecosystem was a net sink of CO2 during 5–6 months and total seasonal uptakes were ?1128 ± 130 and ?1796 ± 217 g CO2 m?2 in 2011 and 2012, respectively. In conclusion, our findings suggest that the annual carbon status of a switchgrass ecosystem can be a small sink to small source in this region if carbon loss from biomass harvesting is considered. However, year‐round measurements over several years are required to assess a long‐term source‐sink status of the ecosystem.  相似文献   

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