The dependence of respiration on photosynthetic substrate supply and temperature: integrating leaf, soil and ecosystem measurements

Interactions between photosynthetic substrate supply and temperature in determining the rate of three respiration components (leaf, belowground and ecosystem respiration) were investigated within three environmentally controlled, Populus deltoides forest bays at Biosphere 2, Arizona. Over 2 months, the atmospheric CO₂ concentration and air temperature were manipulated to test the following hypotheses: (1) the responses of the three respiration components to changes in the rate of photosynthesis would differ both in speed and magnitude; (2) the temperature sensitivity of leaf and belowground respiration would increase in response to a rise in substrate availability; and, (3) at the ecosystem level, the ratio of respiration to photosynthesis would be conserved despite week‐to‐week changes in temperature. All three respiration rates responded to the CO₂ concentration‐induced changes in photosynthesis. However, the proportional change in the rate of leaf respiration was more than twice that of belowground respiration and, when photosynthesis was reduced, was also more rapid. The results suggest that aboveground respiration plays a key role in the overall response of ecosystem respiration to short‐term changes in canopy photosynthesis. The short‐term temperature sensitivity of leaf respiration, measured within a single night, was found to be affected more by developmental conditions than photosynthetic substrate availability, as the Q₁₀ was lower in leaves that developed at high CO₂, irrespective of substrate availability. However, the temperature sensitivity of belowground respiration, calculated between periods of differing air temperature, appeared to be positively correlated with photosynthetic substrate availability. At the ecosystem level, respiration and photosynthesis were positively correlated but the relationship was affected by temperature; for a given rate of daytime photosynthesis, the rate of respiration the following night was greater at 25 than 20°C. This result suggests that net ecosystem exchange did not acclimate to temperature changes lasting up to 3 weeks. Overall, the results of this study demonstrate that the three respiration terms differ in their dependence on photosynthesis and that, short‐ and medium‐term changes in temperature may affect net carbon storage in terrestrial ecosystems.     

Acclimation of photosynthesis,respiration and ecosystem carbon flux of a wetland on Chesapeake Bay,Maryland to elevated atmospheric CO2 concentration

Acclimation of photosynthesis and respiration in shoots and ecosystem carbon dioxide fluxes to rising atmospheric carbon dioxide concentration (C _a ) was studied in a brackish wetland. Open top chambers were used to create test atmospheres of normal ambient and elevated C _a (=normal ambient + 34 Pa CO₂) over mono-specific stands of the C₃ sedge Scirpus olneyi, the dominant C₃ species in the wetland ecosystem, throughout each growing season since April of 1987. Acclimation of photosynthesis and respiration were evaluated by measurements of gas exchange in excised shoots. The impact of elevated C _a on the accumulation of carbon in the ecosystem was determined by ecosystem gas exchange measurements made using the open top chamber as a cuvette.Elevated C _a increased carbohydrate and reduced Rubisco and soluble protein concentrations as well as photosynthetic capacity(A) and dark respiration (R _d ; dry weight basis) in excised shoots and canopies (leaf area area basis) of Scirpus olneyi. Nevertheless, the rate of photosynthesis was stimulated 53% in shoots and 30% in canopies growing in elevated C _a compared to normal ambient concentration. Elevated C _a inhibited R _d measured in excised shoots (–19 to –40%) and in seasonally integrated ecosystem respiration (R _e ; –36 to –57%). Growth of shoots in elevated C _a was stimulated 14–21%, but this effect was not statistically significant at peak standing biomass in midseason. Although the effect of elevated C _a on growth of shoots was relatively small, the combined effect of increased number of shoots and stimulation of photosynthesis produced a 30% stimulation in seasonally integrated gross primary production (GPP). The stimulation of photosynthesis and inhibition of respiration by elevated C _a increased net ecosystem production (NEP=GPP–R _e ) 59% in 1993 and 50% in 1994. While this study consistently showed that elevated C _a produced a significant increase in NEP, we have not identified a correspondingly large pool of carbon below ground.     

Dependence of carbon sequestration on the differential responses of ecosystem photosynthesis and respiration to rain pulses in a semiarid steppe

Precipitation pulses play an important role in regulating ecosystem carbon exchange and balance of semiarid steppe ecosystems. It has been predicted that the frequency of extreme rain events will increase in the future, especially in the arid and semiarid regions. We hypothesize that large rain pulses favor carbon sequestration, while small ones cause more carbon release in the semiarid steppes. To understand the potential response in carbon sequestration capacity of semiarid steppes to the changes in rain pulse size, we conducted a manipulative experiment with five simulated rain pulse sizes (0, 5, 10, 25, and 75 mm) in Inner Mongolia steppe. Our results showed that both gross ecosystem productivity (GEP) and ecosystem respiration (R_e) responded rapidly (within 24 h) to rain pulses and the initial response time was independent of pulse size. However, the time of peak GEP was 1–3 days later than that of R_e, which depended on pulse size. Larger pulses caused greater magnitude and longer duration of variations in GEP and R_e. Differences in the response time of microbes and plants to wetting events constrained the response pattern of heterotrophic (R_h) and autotrophic (R_a) components of R_e following a rain event. R_h contributed more to the increase of R_e in the early stage of rain pulse response, while R_a played an more important role later, and determined the duration of pulse response, especially for large rain events of >10 mm. The distinct responses of ecosystem photosynthesis and respiration to increasing pulse sizes led to a threshold in rain pulse size between 10 and 25 mm, above which post wetting responses favored carbon sequestration. The disproportionate increase of the primary productivity of higher plants, compared with those in the activities of microbial decomposers to larger pulse events suggests that the carbon sequestration capacity of Inner Mongolia steppes will be sensitive to changes in precipitation size distribution rather than just precipitation amount.     

Variations of ecosystem gas exchange in the rain forest mesocosm at Biosphere 2 in response to elevated CO2

The effects of elevated CO₂ on tropical ecosystems were studied in the artificial rain forest mesocosm at Biosphere 2, a large-scale and ecologically diverse experimental facility located in Oracle, Arizona. The ecosystem responses were assessed by comparing the whole-system net gas exchange (NEE) upon changing CO₂ levels from 900 to 450 ppmV. The day-NEE was significantly higher in the elevated CO₂ treatment. In both experiments, the NEE rates were similar to values observed in natural analogue systems. Variations in night-NEE, reflecting both soil CO₂ efflux and plants respiration, covaried with temperature but showed no clear correlation with atmospheric CO₂ levels. After correcting for changes in CO₂ efflux we show that the rain forest net photosynthesis increased in response to increasing atmospheric CO₂. The photosynthetic enhancement was expressed in higher quantum yields, maximum assimilation rates and radiation use efficiency. The results suggest that photosynthesis in large tropical trees is CO₂ sensitive, at least following short exposures of days to weeks. Taken at face value, the data suggest that as a result of anthropogenic emissions of CO₂, tropical rain forests may shift out of steady state, and become a carbon sink at least for short periods. However, a better understanding of the unique conditions and phenomena in Biosphere 2 is necessary before these results are broadly useful.     

Seasonal and annual respiration of a ponderosa pine ecosystem

The net ecosystem exchange of CO₂ between forests and the atmosphere, measured by eddy covariance, is the small difference between two large fluxes of photosynthesis and respiration. Chamber measurements of soil surface CO₂ efflux (F_s), wood respiration (F_w) and foliage respiration (F_f) help identify the contributions of these individual components to net ecosystem exchange. Models developed from the chamber data also provide independent estimates of respiration costs. We measured CO₂ efflux with chambers periodically in 1996–97 in a ponderosa pine forest in Oregon, scaled these measurements to the ecosystem, and computed annual totals for respiration by component. We also compared estimated half-hourly ecosystem respiration at night (F_nc) with eddy covariance measurements. Mean foliage respiration normalized to 10 °C was 0.20 μmol m^–2 (hemi-leaf surface area) s^–1, and reached a maximum of 0.24 μmol m^–2 HSA s^–1 between days 162 and 208. Mean wood respiration normalized to 10 °C was 5.9 μmol m^–3 sapwood s^–1, with slightly higher rates in mid-summer, when growth occurs. There was no significant difference (P > 0.10) between wood respiration of young (45 years) and old trees (250 years). Soil surface respiration normalized to 10 °C ranged from 0.7 to 3.0 μmol m^–2 (ground) s^–1 from days 23 to 329, with the lowest rates in winter and highest rates in late spring. Annual CO₂ flux from soil surface, foliage and wood was 683, 157, and 54 g C m^–2 y^–1, with soil fluxes responsible for 76% of ecosystem respiration. The ratio of net primary production to gross primary production was 0.45, consistent with values for conifer sites in Oregon and Australia, but higher than values reported for boreal coniferous forests. Below-ground carbon allocation (root turnover and respiration, estimated as F_s– litterfall carbon) consumed 61% of GPP; high ratios such as this are typical of sites with more water and nutrient constraints. The chamber estimates were moderately correlated with change in CO₂ storage in the canopy (F_stor) on calm nights (friction velocity u* < 0.25 m s^–1; R² = 0.60); F_stor was not significantly different from summed chamber estimates. On windy nights (u* > 0.25 m s^–1), the sum of turbulent flux measured above the canopy by eddy covariance and F_stor was only weakly correlated with summed chamber estimates (R² = 0.14); the eddy covariance estimates were lower than chamber estimates by 50%.     

Soil and total ecosystem respiration in agricultural fields: effect of soil and crop type

A study was made of the effect of soil and crop type on the soil and total ecosystem respiration rates in agricultural soils in southern Finland. The main interest was to compare the soil respiration rates in peat and two different mineral soils growing barley, grass and potato. Respiration measurements were conducted during the growing season with (1) a closed-dynamic ecosystem respiration chamber, in which combined plant and soil respiration was measured and (2) a closed-dynamic soil respiration chamber which measured only the soil and root-derived respiration. A semi-empirical model including separate functions for the soil and plant respiration components was used for the total ecosystem respiration (TER), and the resulting soil respiration parameters for different soil and crop types were compared. Both methods showed that the soil respiration in the peat soil was 2–3 times as high as that in the mineral soils, varying from 0.11 to 0.36 mg (CO₂) m^–2 s^–1 in the peat soil and from 0.02 to 0.17 mg (CO₂) m^–2 s^–1 in the mineral soils. The difference between the soil types was mainly attributed to the soil organic C content, which in the uppermost 20 cm of the peat soil was 24 kg m^–2, being about 4 times as high as that in the mineral soils. Depending on the measurement method, the soil respiration in the sandy soil was slightly higher than or similar to that in the clay soil. In each soil type, the soil respiration was highest on the grass plots. Higher soil respiration parameter values (R_s0, describing the soil respiration at a soil temperature of 10°C, and obtained by modelling) were found on the barley than on the potato plots. The difference was explained by the different cultivation history of the plots, as the potato plots had lain fallow during the preceding summer. The total ecosystem respiration followed the seasonal evolution in the leaf area and measured photosynthetic flux rates. The 2–3-fold peat soil respiration term as compared to mineral soil indicates that the cultivated peat soil ecosystem is a strong net CO₂ source.     

Carbon sequestration and ecosystem respiration for 4 years in a Scots pine forest

The net exchange of CO₂ (NEE) between a Scots pine (Pinus sylvestris L.) forest ecosystem in eastern Finland and the atmosphere was measured continuously by the eddy covariance (EC) technique over 4 years (1999–2002). The annual temperature coefficient (Q₁₀) of ecosystem respiration (R) for these years, respectively, was 2.32, 2.66, 2.73 and 2.69. The light‐saturated rate of photosynthesis (A_max) was highest in July or August, with an annual average A_max of 10.9, 14.6, 15.3 and 17.1 μmol m^?2 s^?1 in the 4 years, respectively. There was obvious seasonality in NEE, R and gross primary production (GPP), exhibiting a similar pattern to photosynthetically active radiation (PAR) and air temperature. The integrated daily NEE ranged from 2.59 to ?4.97 g C m^?2 day^?1 in 1999, from 2.70 to ?4.72 in 2000, from 2.61 to ?4.71 in 2001 and from 5.27 to ?4.88 in 2002. The maximum net C uptake occurred in July, with the exception of 2000, when it was in June. The interannual variation in ecosystem C flux was pronounced. The length of the growing season, based on net C uptake, was 179, 170, 175 and 176 days in 1999–2002, respectively, and annual net C sequestration was 152, 101, 172 and 205 g C m^?2 yr^?1. It is estimated that ecosystem respiration contributed 615, 591, 752 and 879 g C m^?2 yr^?1 to the NEE in these years, leading to an annual GPP of ?768, ?692, ?924 and ?1084 g C m^?2 yr^?1. It is concluded that temperature and PAR were the main determinants of the ecosystem CO₂ flux. Interannual variations in net C sequestration are predominantly controlled by average air temperature and integrated radiation in spring and summer. Four years of EC data indicate that boreal Scots pine forest ecosystem in eastern Finland acts as a relatively powerful carbon sink. Carbon sequestration may benefit from warmer climatic conditions.     

Epilithic chlorophyll a,photosynthesis, and respiration in control and fertilized reaches of a tundra stream

Photosynthesis and respiration by the epilithic community on cobble in an arctic tundra stream, were estimated from oxygen production and consumption in short-term (4–12 h), light and dark, chamber incubations. Chlorophyll a was estimated at the end of each incubation by quantitatively removing the epilithon from the cobble. Fertilization of the river with phosphate alone moderately increased epilithic chlorophyll a, photosynthesis, and respiration. Fertilization with ammonium sulfate and phosphate, together, greatly increased each of these variables. Generally, under both control and fertilized conditions, epilithic chlorophyll a concentrations (mg m⁻²), photosynthesis, and respiration (mg O₂ m⁻², h⁻¹) were higher in pools than in riffles. Under all conditions, the P/R ratio was consistent at ∼ 1.8 to 2.0. The vigor of epilithic algae in riffles, estimated from assimilation coefficients (mg O₂ [mg Chl a]⁻¹ h⁻¹) was greater than the vigor of epilithic algae in pools. However, due to the greater accumulation of epilithic chlorophyll a in pools, total production (and respiration) in pools exceeded that in riffles. The epilithic community removed both ammonium and nitrate from water in chambers. Epilithic material, scoured by high discharge in response to storm events and suspended in the water column, removed ammonium and may have increased nitrate concentrations in bulk river water. However, these changes were small compared to the changes exerted by attached epilithon.     

Total and component carbon fluxes of a Scots pine ecosystem from chamber measurements and eddy covariance

BACKGROUND AND AIMS: Distinguishing between, and quantifying, the different components of ecosystem C fluxes is critical in predicting the responses of ecosystem C cycling to climate change. The aims of this study were to quantify the photosynthetic and respiratory fluxes of a 50-year-old Scots pine (Pinus sylvestris) ecosystem, and to distinguish respiration of branches with needles from that of stems, and that of soil. METHODS: The CO2 flux of the ecosystem was continuously measured using the eddy covariance (EC) method, and its components (respiration and photosynthesis of a branch with needles, stem and soil surface) were measured with an automated chamber system, from 2001 to 2004. KEY RESULTS: All values below are chamber based. The average temperature coefficient (Q10) of respiration was 2.7, 2.2 and 4.0, respectively, for branch (Rbran), stem (Rstem) and the soil surface (Rsoil). Respiration at a reference temperature of 15 degrees C (R15) was 1.27, 0.49 and 4.02 micromol CO2 m(-2) ground s(-1) for the three components, respectively. Over 4 years, the annual Rbran, Rstem and Rsoil ranged from 196 to 256, 56 to 83 and 439 to 598 g C m(-2) ground year(-1), respectively, with a 4-year average of 227, 72 and 507 g C m(-2) ground year(-1). Annual ecosystem respiration (Reco) was 731, 783, 909 and 751 g C m(-2) ground year(-1) in years 2001-2004, respectively, gross primary production (GPP) was 922, 1030, 1138 and 1001 g C m(-2) ground year(-1), and net ecosystem production (NEP) was 191, 247, 229 and 251 g C m(-2) ground year(-1). The average contribution of Rbran, Rstem and Rsoil to Reco was 29, 9 and 62 %, respectively. Overstorey photosynthesis accounted for 96 % of GPP. The average Reco/GPP ratio was 0.78. Net primary production (NPP) in the 4 years was 469, 581, 600 and 551 g C m(-2) year(-1), respectively, with the NPP/GPP ratio 0.54 averaged over the years. CONCLUSIONS: Respiration from the soil is the dominant component of ecosystem respiration. Differences between years in Reco were due to differences in temperature during the growing season. Rsoil was more sensitive to temperature than Rbran and Rstem, and differences in Rsoil were responsible for the differences in Reco between years.     

Warmer and drier conditions stimulate respiration more than photosynthesis in a boreal peatland ecosystem: Analysis of automatic chambers and eddy covariance measurements

Continuous half‐hourly net CO₂ exchange measurements were made using nine automatic chambers in a treed fen in northern Alberta, Canada from June–October in 2005 and from May–October in 2006. The 2006 growing season was warmer and drier than in 2005. The average chamber respiration rates normalized to 10 °C were much higher in 2006 than in 2005, while calculations of the temperature sensitivity (Q₁₀) values were similar in the two years. Daytime average respiration values were lower than the corresponding, temperature‐corrected respiration rates calculated from night‐time chamber measurements. From June to September, the season‐integrated estimates of chamber photosynthesis and respiration were 384 and 590 g C m^?2, respectively in 2006, an increase of 100 and 203 g C m^?2 over the corresponding values in 2005. The season‐integrated photosynthesis and respiration rates obtained using the eddy covariance technique, which included trees and a tall shrub not present in the chambers, were 720 and 513 g C m^?2, respectively, in 2006, an increase of 50 and 125 g C m^?2 over the corresponding values in 2005. While both photosynthesis and respiration rates were higher in the warmer and drier conditions of 2006, the increase in respiration was more than twice the increase in photosynthesis.     

Effects of salinity on growth, photosynthesis and respiration in a freshwater alga Rhizoclonium riparium (Chlorophyceae, Cladophorales)

A freshwater green alga, Rhizoclonium riparium (Roth) Harvey, was found to grow in diluted seawater with salinities (PSU) from 0.1 to 34.0 (0.1–34.0 S). It grew best at 13.6 S and least at 0.1 S which was the least salinity reported in its habitat. Net photosynthetic oxygen production of R. riparium rose with salinity up to 34.0. However, in the medium adjusted at pH 8.1. the net photosynthesis rose at low ranges of salinity and was almost at the same level in all ranges of salinities examined. The net photosynthesis was increased by the addition of bicarbonate in the medium. Respiratory oxygen consumption did not rise with the increase of external salinities from 0.1 to 34.0. The results indicate that R. riparium can grow by increasing net photosynthesis in diluted seawater in which the pH value is suitable for effective bicarbonate supply to photosynthesis.     

Seasonal and interannual variation in carbon dioxide exchange and carbon balance in a northern temperate grassland

Net ecosystem carbon dioxide (CO₂) exchange (NEE) was measured in a northern temperate grassland near Lethbridge, Alberta, Canada for three growing seasons using the eddy covariance technique. The study objectives were to document how NEE and its major component processes—gross photosynthesis (GPP) and total ecosystem respiration (TER)—vary seasonally and interannually, and to examine how environmental and physiological factors influence the annual C budget. The greatest difference among the three study years was the amount of precipitation received. The annual precipitation for 1998 (481.7 mm) was significantly above the 1971–2000 mean (± SD, 377.9 ± 97.0 mm) for Lethbridge, whereas 1999 (341.3 mm) was close to average, and 2000 (275.5 mm) was significantly below average. The high precipitation and soil moisture in 1998 allowed a much higher GPP and an extended period of net carbon gain relative to 1999 and 2000. In 1998, the peak NEE was a gain of 5 g C m^?2 d^?1 (day 173). Peak NEE was lower and also occurred earlier in the year on days 161 (3.2 g C m^?2 d^?1) and 141 (2.4 g C m^?2 d^?1) in 1999 and 2000, respectively. Change in soil moisture was the most important ecological factor controlling C gain in this grassland ecosystem. Soil moisture content was positively correlated with leaf area index (LAI). Gross photosynthesis was strongly correlated with changes in both LAI and canopy nitrogen (N) content. Maximum GPP (A_max: value calculated from a rectangular hyperbola fitted to the relationship between GPP and incident photosynthetic photon flux density (PPFD)) was 27.5, 12.9 and 8.6 µmol m^?2 s^?1 during 1998, 1999 and 2000, respectively. The apparent quantum yield also differed among years at the time of peak photosynthetic activity, with calculated values of 0.0254, 0.018 and 0.018 during 1998, 1999 and 2000, respectively. The ecosystem accumulated a total of 111.9 g C m^?2 from the time the eddy covariance measurements were initiated in June 1998 until the end of December 2000, with most of that C gained during 1998. There was a net uptake of almost 21 g C m^?2 in 1999, whereas a net loss of 18 g C m^?2 was observed in 2000. The net uptake of C during 1999 was the combined result of slightly higher GPP (287.2 vs. 272.3 g C m^?2 year^?1) and lower TER (266.6 vs. 290.4 g C m^?2 year^?1) than occurred in 2000.     

Stimulation of both photosynthesis and respiration in response to warmer and drier conditions in a boreal peatland ecosystem

Peatland ecosystems have been consistent carbon (C) sinks for millennia, but it has been predicted that exposure to warmer temperatures and drier conditions associated with climate change will shift the balance between ecosystem photosynthesis and respiration providing a positive feedback to atmospheric CO₂ concentration. Our main objective was to determine the sensitivity of ecosystem photosynthesis, respiration and net ecosystem production (NEP) measured by eddy covariance, to variation in temperature and water table depth associated with interannual shifts in weather during 2004–2009. Our study was conducted in a moderately rich treed fen, the most abundant peatland type in western Canada, in a region (northern Alberta) where peatland ecosystems are a significant landscape component. During the study, the average growing season (May–October) water depth declined approximately 38 cm, and temperature [expressed as cumulative growing degree days (GDD, March–October)] varied approximately 370 GDD. Contrary to previous predictions, both ecosystem photosynthesis and respiration showed similar increases in response to warmer and drier conditions. The ecosystem remained a strong net sink for CO₂ with an average NEP (± SD) of 189 ± 47 g C m^?2 yr^?1. The current net CO₂ uptake rates were much higher than C accumulation in peat determined from analyses of the relationship between peat age and cumulative C stock. The balance between C addition to, and total loss from, the top 0–30 cm depth (peat age range 0–70 years) of shallow peat cores averaged 43 ± 12 g C m^?2 yr^?1. The apparent long‐term average rate of net C accumulation in basal peat samples was 19–24 g C m^?2 yr^?1. The difference between current rates of net C uptake and historical rates of peat accumulation is likely a result of vegetation succession and recent increases in tree establishment and productivity.     

Ecosystem–atmosphere exchange of CH4 and N2O and ecosystem respiration in wetlands in the Sanjiang Plain, Northeastern China

Natural wetlands are critically important to global change because of their role in modulating atmospheric concentrations of CO₂, CH₄, and N₂O. One 4‐year continuous observation was conducted to examine the exchanges of CH₄ and N₂O between three wetland ecosystems and the atmosphere as well as the ecosystem respiration in the Sanjiang Plain in Northeastern China. From 2002 to 2005, the mean annual budgets of CH₄ and N₂O, and ecosystem respiration were 39.40 ± 6.99 g C m^?2 yr^?1, 0.124 ± 0.05 g N m^?2 yr^?1, and 513.55 ± 8.58 g C m^?2 yr^?1 for permanently inundated wetland; 4.36 ± 1.79 g C m^?2 yr^?1, 0.11 ± 0.12 g N m^?2 yr^?1, and 880.50 ± 71.72 g C m^?2 yr^?1 for seasonally inundated wetland; and 0.21 ± 0.1 g C m^?2 yr^?1, 0.28 ± 0.11 g N m^?2 yr^?1, and 1212.83 ± 191.98 g C m^?2 yr^?1 for shrub swamp. The substantial interannual variation of gas fluxes was due to the significant climatic variability which underscores the importance of long‐term continuous observations. The apparent seasonal pattern of gas emissions associated with a significant relationship of gas fluxes to air temperature implied the potential effect of global warming on greenhouse gas emissions from natural wetlands. The budgets of CH₄ and N₂O fluxes and ecosystem respiration were highly variable among three wetland types, which suggest the uncertainties in previous studies in which all kinds of natural wetlands were treated as one or two functional types. New classification of global natural wetlands in more detailed level is highly expected.     

Ecosystem CO2 exchange and plant biomass in the littoral zone of a boreal eutrophic lake

• 1 In order to study the dynamics of primary production and decomposition in the lake littoral, an interface zone between the pelagial, the catchment and the atmosphere, we measured ecosystem/atmosphere carbon dioxide (CO₂) exchange in the littoral zone of an eutrophic boreal lake in Finland during two open water periods (1998–1999). We reconstructed the seasonal net CO₂ exchange and identified the key factors controlling CO₂ dynamics. The seasonal net ecosystem exchange (NEE) was related to the amount of carbon accumulated in plant biomass.
• 2 In the continuously inundated zones, spatial and temporal variation in the density of aerial shoots controlled CO₂ fluxes, but seasonal net exchange was in most cases close to zero. The lower flooded zone had a net CO₂ uptake of 1.8–6.2 mol m^?2 per open water period, but the upper flooded zone with the highest photosynthetic capacity and above‐ground plant biomass, had a net CO₂ loss of 1.1–7.1 mol m^?2 per open water period as a result of the high respiration rate. The excess of respiration can be explained by decomposition of organic matter produced on site in previous years or leached from the catchment.
• 3 Our results from the two study years suggest that changes in phenology and water level were the prime cause of the large interannual difference in NEE in the littoral zone. Thus, the littoral is a dynamic buffer and source for the load of allochthonous and autochthonous carbon to small lakes.

     

A comparative study of the effects of NaCl salinity on respiration, photosynthesis, and leaf extension growth in Beta vulgaris L. (sugar beet)

Abstract. Three parameters influencing the capacity for carbon accumulation, i.e. photosynthesis, respiration, and leaf extension growth, were studied in Beta vulgaris L. (sugar beet) cultured in nutrient solution containing 0.5 to 500 mol m⁻³ NaCl. Leaf extension growth was the parameter most sensitive to salinity: the initial rate of leaf extension and final leaf length each declined linearly with increase in external NaCl concentration. Photosynthetic O₂ evolution of thin leaf slices did not decline until salinity levels reached 350 to 500 mol m⁻³ NaCl, while respiratory O₂ consumption was not affected by salinity throughout the range. The results suggest that the influence of salinity on the capacity for carbon accumulation in B. vulgaris occurs primarily through reduction in the area of photosynthetic surface.     

Importance of short-term dynamics in carbon isotope ratios of ecosystem respiration (delta13C(R)) in a Mediterranean oak woodland and linkage to environmental factors

Temporal dynamics in carbon isotope ratios of ecosystem respiration (delta13C(R)) were evaluated on hourly, daily and annual timescales in a Mediterranean woodland. Emphasis was given to the periods of transition from wet to dry season and vice versa, when the system turns from a net carbon sink to a source. The constancy of nocturnal delta13C(R) was tested. The relationship between delta13C(R) (determined through Keeling plots) and environmental factors was evaluated through time-lag analysis. Delta13C(R) exhibited high annual variation (> 7). During the transition periods, delta13C(R) correlated significantly with factors influencing photosynthetic discrimination, soil respiration, and whole-canopy conductance. Time-lags differed between below- and above-ground variables, and between seasons. A shift in regression parameters with environmental factors indicated seasonal differences in ecosystem responsiveness (e.g. temperature acclimation). Delta13C(R) exhibited substantial nocturnal enrichment (> 4) from dusk to dawn. These data indicate pronounced short-term dynamics in delta13C(R) at hourly to daily timescales and a modulated response to environmental drivers. Substantial short-term changes in nocturnal delta13C(R) may have important implications for the sampling protocols of nocturnal Keeling plots.     

Response of ecosystem carbon exchange to warming and nitrogen addition during two hydrologically contrasting growing seasons in a temperate steppe

A large remaining source of uncertainty in global model predictions of future climate is how ecosystem carbon (C) cycle feedbacks to climate change. We conducted a field manipulative experiment of warming and nitrogen (N) addition in a temperate steppe in northern China during two contrasting hydrological growing seasons in 2006 [wet with total precipitation 11.2% above the long‐term mean (348 mm)] and 2007 (dry with total precipitation 46.7% below the long‐term mean). Irrespective of strong intra‐ and interannual variations in ecosystem C fluxes, responses of ecosystem C fluxes to warming and N addition did not change between the two growing seasons, suggesting independence of warming and N responses of net ecosystem C exchange (NEE) upon hydrological variations in the temperate steppe. Warming had no effect on NEE or its two components, gross ecosystem productivity (GEP) and ecosystem respiration (ER), whereas N addition stimulated GEP but did not affect ER, leading to positive responses of NEE. Similar responses of NEE between the two growing seasons were due to changes in both biotic and abiotic factors and their impacts on ER and GEP. In the wet growing season, NEE was positively correlated with soil moisture and forb biomass. Negative effects of warming‐induced water depletion could be ameliorated by higher forb biomass in the warmed plots. N addition increased forb biomass but did not affect soil moisture, leading to positive effect on NEE. In the dry growing season, NEE showed positive dependence on grass biomass but negative dependence on forb biomass. No changes in NEE in response to warming could result from water limitation on both GEP and ER as well as little responses of either grass or forb biomass. N addition stimulated grass biomass but reduced forb biomass, leading to the increase in NEE. Our findings highlight the importance of changes in abiotic (soil moisture, N availability) and biotic (growth of different plant functional types) in mediating the responses of NEE to climatic warming and N enrichment in the semiarid temperate steppe in northern China.     

Diurnal, seasonal and annual variation in the net ecosystem CO2 exchange of a desert shrub community (Sarcocaulescent) in Baja California, Mexico

Estimates of net ecosystem exchange (NEE) of CO₂ have been measured on a variety of ecosystems world wide including grasslands, savannahs, boreal, pine, deciduous, Mediterranean and tropical rain forests as well as arctic tundra. While there have been numerous comparisons between net primary productivity of arid and semiarid grasslands and shrublands, notably lacking are estimates of NEE with a few exceptions. The objective of this study was to characterize the seasonal and annual carbon flux of a desert shrub ecosystem using the eddy covariance technique to determine the sensitivity of the system to the timing and varying amounts of precipitation. Measurements began in July of 2001, a year with 339 mm of rainfall, considerably above the long‐term average of 174 mm and preceded by 2 years of below average rainfall (50–62 mm). Over the 2 complete years of measurements, precipitation was 147 and 197 mm in 2002 and 2003, respectively. In all years, the majority of the precipitation fell between August and September. The site was a sink of ?39 g C m^?2 yr^?1 in 2002 with a relatively strong uptake in the early part of the year and reduced uptake after the suboptimal rainfall in September. This contrasts with 2003 when the ecosystem took up ?52 g C m^?2 yr^?1 concentrated in the fall after significant rain in August and September. Likely, extremely low rainfall years would result in a carbon loss while a strengthening of the typical winter secondary peak in precipitation (notably absent in the 2 years of measurements) may extend uptake into the spring resulting in more carbon accumulation. The system appears to be buffered against variations in annual rainfall attributed to water storage in the stems and roots.