Climatic influences on net ecosystem CO<Subscript>2</Subscript> exchange during the transition from wintertime carbon source to springtime carbon sink in a high-elevation,subalpine forest

The transition between wintertime net carbon loss and springtime net carbon assimilation has an important role in controlling the annual rate of carbon uptake in coniferous forest ecosystems. We studied the contributions of springtime carbon assimilation to the total annual rate of carbon uptake and the processes involved in the winter-to-spring transition across a range of scales from ecosystem CO₂ fluxes to chloroplast photochemistry in a coniferous, subalpine forest. We observed numerous initiations and reversals in the recovery of photosynthetic CO₂ uptake during the initial phase of springtime recovery in response to the passage of alternating warm- and cold-weather systems. Full recovery of ecosystem carbon uptake, whereby the 24-h cumulative sum of NEE (NEE_daily) was consistently negative, did not occur until 3–4 weeks after the first signs of photosynthetic recovery. A key event that preceded full recovery was the occurrence of isothermality in the vertical profile of snow temperature across the snow pack; thus, providing consistent daytime percolation of melted snow water through the snow pack. Interannual variation in the cumulative annual NEE (NEE_annual) was mostly explained by variation in NEE during the snow-melt period (NEE_snow-melt), not variation in NEE during the snow-free part of the growing season (NEE_snow-free). NEE_snow-melt was highest in those years when the snow melt occurred later in the spring, leading us to conclude that in this ecosystem, years with earlier springs are characterized by lower rates of NEE_annual, a conclusion that contrasts with those from past studies in deciduous forest ecosystems. Using studies on isolated branches we showed that the recovery of photosynthesis occurred through a series of coordinated physiological and biochemical events. Increasing air temperatures initiated recovery through the upregulation of PSII electron transport caused in part by disengagement of thermal energy dissipation by the carotenoid, zeaxanthin. The availability of liquid water permitted a slightly slower recovery phase involving increased stomatal conductance. The most rate-limiting step in the recovery process was an increase in the capacity for the needles to use intercellular CO₂, presumably due to slow recovery of Rubisco activity. Interspecific differences were observed in the timing of photosynthetic recovery for the dominant tree species. The results of our study provide (1) a context for springtime CO₂ uptake within the broader perspective of the annual carbon budget in this subalpine forest, and (2) a mechanistic explanation across a range of scales for the coupling between springtime climate and the carbon cycle of high-elevation coniferous forest ecosystems.     

The interaction of biotic and abiotic factors at multiple spatial scales affects the variability of CO<Subscript>2</Subscript> fluxes in polar environments

Climate change may turn Arctic biomes from carbon sinks into sources and vice versa, depending on the balance between gross ecosystem photosynthesis, ecosystem respiration (ER) and the resulting net ecosystem exchange (NEE). Photosynthetic capacity is species specific, and thus, it is important to quantify the contribution of different target plant species to NEE and ER. At Ny Ålesund (Svalbard archipelago, Norway), we selected different Arctic tundra plant species and measured CO₂ fluxes at plot scale and photosynthetic capacity at leaf scale. We aimed to analyze trends in CO₂ fluxes during the transition seasons (beginning vs. end of the growing season) and assess which abiotic (soil temperature, soil moisture, PAR) and biotic (plot type, phenology, LAI, photosynthetic capacity) factors influenced CO₂ emissions. NEE and ER differed between vegetation communities. All communities acted as CO₂ sources, with higher source strength at the beginning than at the end of the growing season. The key factors affecting NEE were soil temperature, LAI and species-specific photosynthetic capacities, coupled with phenology. ER was always influenced by soil temperature. Measurements of photosynthetic capacity indicated different responses among species to light intensity, as well as suggesting possible gains in response to future increases in atmospheric CO₂ concentrations. Species-specific adaptation to low temperatures could trigger significant feedbacks in a climate change context. Our data highlight the need to quantify the role of dominant species in the C cycle (sinks or sources), as changes of vegetation composition or species phenology in response to climate change may have great impact on the regional CO₂ balance.     

黄河三角洲芦苇湿地生长季净生态系统CO2交换及其环境调控机制

采用涡度相关法,对2011年生长季的黄河三角洲芦苇湿地净生态系统CO₂交换(NEE)进行了观测,研究湿地NEE的变化规律及其影响因子.结果表明: 不同月份芦苇湿地的NEE日变化均呈“U”形曲线,CO₂最大净吸收率和释放率的日均值分别为(0.44±0.03)和(0.16±0.01) mg CO₂·m^-2·s^-1;芦苇湿地NEE、生态系统呼吸(R_eco)、总初级生产力(GPP)的季节变化均呈现生长旺季(7-9月)较高、生长初期(5-6月)和生长末期(10-11月)较低的趋势;R_eco和NEE在8月达到峰值,GPP在7月达到峰值.芦苇湿地生态系统的CO₂交换受到光合有效辐射(PAR)、土壤温度(T_s)和土壤体积含水量(SWC)的共同影响.白天NEE与PAR呈直角双曲线关系;5 cm深处T_s与夜间生态系统呼吸(R_eco,n)呈指数关系,生态系统呼吸的温度敏感性(Q₁₀)为2.30,SWC和T_s是影响芦苇湿地R_eco,n的主要因子.在整个生长季,黄河三角洲芦苇湿地生态系统是一个明显的CO₂的汇,总净固碳量为780.95 g CO₂·m^-2.     

青海湖北岸高寒草甸草原生态系统CO2通量特征及其驱动因子

 草甸草原是青藏高原的重要植被类型, 与其他植被类型相比, 其碳交换过程和驱动机理的研究仍较薄弱。利用青海湖东北岸草甸草原的涡度相关系统观测的连续数据(2010年7月1日–2011年6月30日), 分析了草甸草原CO₂通量特征及其驱动因子。结果表明: 草甸草原净生态系统CO₂交换量(NEE)在植物生长季的5–9月, 其日变化主要受控于光合光量子通量密度(PPFD); 而非生长季(10月21日–4月19日)和生长季初(4月下旬)、末期(10月中上旬) NEE的日变化主要受气温(T_a)的影响。CO₂
日最大吸收值和释放值分别出现在7月1日(11.37 g CO₂·m^–2·d^–1)和10月21日(4.04 g CO₂·m^–2·d^–1)。逐日NEE主要受控于T_a, 两者关系可用指数线性(explinear)方程表示(R² = 0.54, p < 0.01)。叶面积指数(LAI)和增强型植被指数(EVI)对逐日NEE的影响表现为渐近饱和型, LAI和T_a交互作用明显(p < 0.05), EVI的主效应强烈(p < 0.001)。生态系统的呼吸熵(Q₁₀)为2.42, 总呼吸(R_eco)约占总初级生产力(GPP)的74%。生长季适度的昼夜温差(<14.8 ℃)有利于系统的碳蓄积。研究时段该草甸草原作为碳汇从大气吸收271.31 g CO₂· m^–2。     

Carbon sequestration in a high-elevation, subalpine forest

We studied net ecosystem CO₂ exchange (NEE) dynamics in a high‐elevation, subalpine forest in Colorado, USA, over a two‐year period. Annual carbon sequestration for the forest was 6.71 mol C m^?2 (80.5 g C m^?2) for the year between November 1, 1998 and October 31, 1999, and 4.80 mol C m^?2 (57.6 g C m^?2) for the year between November 1, 1999 and October 31, 2000. Despite its evergreen nature, the forest did not exhibit net CO₂ uptake during the winter, even during periods of favourable weather. The largest fraction of annual carbon sequestration occurred in the early growing‐season; during the first 30 days of both years. Reductions in the rate of carbon sequestration after the first 30 days were due to higher ecosystem respiration rates when mid‐summer moisture was adequate (as in the first year of the study) or lower mid‐day photosynthesis rates when mid‐summer moisture was not adequate (as in the second year of the study). The lower annual rate of carbon sequestration during the second year of the study was due to lower rates of CO₂ uptake during both the first 30 days of the growing season and the mid‐summer months. The reduction in CO₂ uptake during the first 30 days of the second year was due to an earlier‐than‐normal spring warm‐up, which caused snow melt during a period when air temperatures were lower and atmospheric vapour pressure deficits were higher, compared to the first 30 days of the first year. The reduction in CO₂ uptake during the mid‐summer of the second year was due to an extended drought, which was accompanied by reduced latent heat exchange and increased sensible heat exchange. Day‐to‐day variation in the daily integrated NEE during the summers of both years was high, and was correlated with frequent convective storm clouds and concomitant variation in the photosynthetic photon flux density (PPFD). Carbon sequestration rates were highest when some cloud cover was present, which tended to diffuse the photosynthetic photon flux, compared to periods with completely clear weather. The results of this study are in contrast to those of other studies that have reported increased annual NEE during years with earlier‐than‐normal spring warming. In the current study, the lower annual NEE during 2000, the year with the earlier spring warm‐up, was due to (1) coupling of the highest seasonal rates of carbon sequestration to the spring climate, rather than the summer climate as in other forest ecosystems that have been studied, and (2) delivery of snow melt water to the soil when the spring climate was cooler and the atmosphere drier than in years with a later spring warm‐up. Furthermore, the strong influence of mid‐summer precipitation on CO₂ uptake rates make it clear that water supplied by the spring snow melt is a seasonally limited resource, and summer rains are critical for sustaining high rates of annual carbon sequestration.     

Winter photosynthetic activity of twenty temperate semi-desert sand grassland species

The winter photosynthetic activity (quantified by net CO(2) assimilation rates and chlorophyll (Chl) a fluorescence parameters) of 20 plant species (including two lichens and two mosses) of a Hungarian temperate semi-desert sand grassland was determined on one occasion per year in 1984, 1989 and 1994. Throughout winter, the overwintering green shoots, leaves or thalli were regularly exposed to below zero temperatures at night and daytime temperatures of 0-5 degrees C. In situ tissue temperature varied between -2.1 and +6.9 degrees C and the photosynthetic photon flux density (PPFD) between 137 and 351 micromol m(-2)s(-1). Under these conditions 18 of the grassland species exhibited photosynthetic CO(2) uptake (range: vascular plants ca. 0.2-3.8 micromol m(-2)s(-1), cryptogams 0.3-2.79 micromol kg(-1)s(-1)) and values of 0.9-5.1 of the Chl fluorescence decrease ratio R(Fd). In 1984, Festuca vaginata and Sedum sexangulare had net CO(2) assimilation at leaf temperatures of -0.85 to -1.2 degrees C. In 1989, all species except Cladonia furcata showed net CO(2) assimilation at tissue temperatures of 0 to +3.3 degrees C, with the highest rates observed in Poa bulbosa and F. vaginata. The latter showed a net CO(2) assimilation saturation at a PPFD of 600 micromol m(-2)s(-1) and a temperature optimum between +5 and +18 degrees C. At the 1994 measurements, the photosynthetic rates were higher at higher tissue water contents. The two mosses and lichens had a net photosynthesis (range: 1.1-2.79 micromol CO(2)kg(-1)s(-1)) at 2 degrees C tissue temperature and at 4-5 degrees C air temperature. Ca. 80% of the vascular grassland plant species maintained a positive C-balance during the coldest periods of winter, with photosynthetic rates of 1.5-3.8 micromol CO(2)m(-2)s(-1). In an extremely warm beginning March of the relatively warm winter of 2006/2007, the dicotyledonous plants had much higher CO(2) assimilation rates on a Chl (range 6-14.9 micromol g(-1)Chl s(-1)) and on a dry weight basis (9-48 micromol kg(-1)dw s(-1)) than in the cold winter of 1994. However, the assimilation rates of the three investigated cryptogams (Tortula and two Cladonia) and the two grasses Festuca and Poa were not affected by this increase. The results indicate that the photosynthetic activity of temperate semi-desert sand grassland species can help somewhat in slowing the general CO(2) rise in winter and function as a potential carbon sink of the investigated semi-desert Hungarian grassland species.     

Greater Abundance of <Emphasis Type="Italic">Betula nana</Emphasis> and Early Onset of the Growing Season Increase Ecosystem CO<Subscript>2</Subscript> Uptake in West Greenland

Expansion of deciduous shrubs is a common observation throughout the Arctic, with implications for carbon (C) cycling. Shrubs may increase net ecosystem C uptake through greater leaf area and gross ecosystem photosynthesis (GEP), and/or through cooler summer soils and reduced ecosystem respiration (ER). We used a space-for-time substitution combined with experimental warming at a Low Arctic site in West Greenland to examine the biophysical effects of increased temperature and Betula nana abundance on ecosystem CO₂ exchange. Communities dominated by Betula were much stronger C sinks than graminoid communities due to greater GEP and lower ER. The warming treatment had little effect on GEP, ER, or net ecosystem CO₂ exchange (NEE). The start of the growing season has been advancing at our study site, as indicated by long-term observations of plant phenology. In a retrospective analysis, we estimate that earlier onset of the growing season has increased the strength of the ecosystem C sink at rates of 1.3 and 2.1 g C m^?2 y^?1 in Betula and graminoid tundra, respectively, since 2002. However, earlier, and presumably longer, growing seasons may be associated with greater potential for drought stress. Our data suggest that mid-summer drought-induced GEP declines may partially offset C gains associated with an earlier start to the growing season. Our results suggest greater deciduous shrub abundance and longer growing seasons will likely lead to greater net C uptake in our study area, while highlighting important complexities associated with drought and plant community composition.     

Temperature controls ecosystem CO2 exchange of an alpine meadow on the northeastern Tibetan Plateau

Alpine ecosystems are extremely vulnerable to climate change. To address the potential variability of the responses of alpine ecosystems to climate change, we examined daily CO₂ exchange in relation to major environmental variables. A dataset was obtained from an alpine meadow on the Qinghai‐Tibetan Plateau from eddy covariance measurements taken over 3 years (2002–2004). Path analysis showed that soil temperature at 5 cm depth (T_s5) had the greatest effect on daily variation in ecosystem CO₂ exchange all year around, whereas photosynthetic photon flux density (PPFD) had a high direct effect on daily variation in CO₂ flux during the growing season. The combined effects of temperature and light regimes on net ecosystem CO₂ exchange (NEE) could be clearly categorized into three areas depending on the change in T_s5: (1) almost no NEE change irrespective of variations in light and temperature when T_s5 was below 0 °C; (2) an NEE increase (i.e. CO₂ released from the ecosystem) with increasing T_s5, but little response to variation in light regime when 0 °C≤T_s5≤8 °C; and (3) an NEE decrease with increase in T_s5 and PPFD when T_s5 was approximately >8 °C. The highest daily net ecosystem CO₂ uptake was observed under the conditions of daily mean T_s5 of about 15 °C and daily mean PPFD of about 50 mol m⁻² day⁻¹. The results suggested that temperature is the most critical determinant of CO₂ exchange in this alpine meadow ecosystem and may play an important role in the ecosystem carbon budget under future global warming conditions.     

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

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.     

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

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

The response of the high altitude C(4) grass Muhlenbergia montana (Nutt.) A.S. Hitchc. to long- and short-term chilling.

The acclimation of C(4) photosynthesis to low temperature was studied in the montane grass Muhlenbergia montana in order to evaluate inherent limitations in the C(4) photosynthetic pathway following chilling. Plants were grown in growth cabinets at 26 degrees C days, but at night temperatures of either 16 degrees C (the control treatment), 4 degrees C for at least 28 nights (the cold-acclimated treatment), or 1 night (the cold-stress treatment). Below a measurement temperature of 25 degrees C, little difference in the thermal response of the net CO(2) assimilation rate (A) was observed between the control and cold-acclimated treatment. By contrast, above 30 degrees C, A in the cold-acclimated treatment was 10% greater than in the control treatment. The temperature responses of Rubisco activity and net CO(2) assimilation rate were similar below 22 degrees C, indicating high metabolic control of Rubisco over the rate of photosynthesis at cool temperatures. Analysis of the response of A to intercellular CO(2) level further supported a major limiting role for Rubisco below 20 degrees C. As temperature declined, the CO(2) saturated plateau of A exhibited large reductions, while the initial slope of the CO(2) response was little affected. This type of response is consistent with a Rubisco limitation, rather than limitations in PEP carboxylase capacity. Stomatal limitations at low temperature were not apparent because photosynthesis was CO(2) saturated below 23 degrees C at air levels of CO(2). In contrast to the response of photosynthesis to temperature and CO(2) in plants acclimated for 4 weeks to low night temperature, plants exposed to 4 degrees C for one night showed substantial reduction in photosynthetic capacity at temperatures above 20 degrees C. Because these reductions were at both high and low CO(2), enzymes associated with the C(4) carbon cycle were implicated as the major mechanisms for the chilling inhibition. These results demonstrate that C(4) plants from climates with low temperature during the growing season can fully acclimate to cold stress given sufficient time. This acclimation appears to involve reversal of injury to the C(4) cycle following initial exposure to low temperature. By contrast, carbon gain at low temperatures generally appears to be constrained by the carboxylation capacity of Rubisco, regardless of acclimation time. The inability to overcome the Rubisco limitation at low temperature may be an inherent limitation restricting C(4) photosynthetic performance in cooler climates.     

Water-mediated responses of ecosystem carbon fluxes to climatic change in a temperate steppe

Global warming and a changing precipitation regime could have a profound impact on ecosystem carbon fluxes, especially in arid and semiarid grasslands where water is limited. A field experiment manipulating temperature and precipitation has been conducted in a temperate steppe in northern China since 2005. A paired, nested experimental design was used, with increased precipitation as the primary factor and warming simulated by infrared radiators as the secondary factor. The results for the first 2 yr showed that gross ecosystem productivity (GEP) was higher than ecosystem respiration, leading to net C sink (measured by net ecosystem CO(2) exchange, NEE) over the growing season in the study site. The interannual variation of NEE resulted from the difference in mean annual precipitation. Experimental warming reduced GEP and NEE, whereas increased precipitation stimulated ecosystem C and water fluxes in both years. Increased precipitation also alleviated the negative effect of experimental warming on NEE. The results demonstrate that water availability plays a dominant role in regulating ecosystem C and water fluxes and their responses to climatic change in the temperate steppe of northern China.     

Modelling the interannual variability of net ecosystem CO2 exchange at a subarctic sedge fen

This paper presents an empirical model of net ecosystem CO₂ exchange (NEE) developed for a subarctic fen near Churchill, Manitoba. The model with observed data helps explain the interannual variability in growing season NEE. Five years of tower‐flux data are used to test and examine the seasonal behaviour of the model simulations. Processes controlling the observed interannual variability of CO₂ exchange at the fen are examined by exploring the sensitivity of the model to changes in air temperature, precipitation and leaf area index. Results indicate that the sensitivity of NEE to changing environmental controls is complex and varies interannually depending on the initial conditions of the wetland. Changes in air temperature and the timing of precipitation events have a strong influence on NEE, which is largely manifest in gross ecosystem photosynthesis (GEP). Climate change scenarios indicate that warmer air temperatures will increase carbon acquisition during wet years but may act to reduce wetland carbon storage in years that experience a large water deficit early in the growing season. Model simulations for this subarctic sedge fen indicate that carbon acquisition is greatest during wet and warm conditions. This suggests therefore that carbon accumulation was greatest at this subarctic fen during its early developmental stages when hydroclimatic conditions were relatively wet and warm at approximately 2500 years before present.     

Interannual variability in net CO2 exchange of a native tallgrass prairie

Year‐round eddy covariance flux measurements were made in a native tallgrass prairie in north‐central Oklahoma, USA during 1997–2000 to quantify carbon exchange and its interannual variability. This prairie is dominated by warm season C₄ grasses. The soil is a relatively shallow silty clay loam underlined with a heavy clay layer and a limestone bedrock. During the study period, the prairie was burned in the spring of each year, and was not grazed. In 1997 there was adequate soil moisture through the growing season, but 1998 had two extended periods of substantially low soil moisture (with concurrent high air temperatures and vapor pressure deficits), one early and one later in the growing season. There was also moisture stress in 1999, but it was less severe and occurred later in the season. The annual net ecosystem CO₂ exchange, NEE (before including carbon loss during the burn) was 274, 46 and 124 g C m ^{? 2} yr ^{? 1} in 1997, 1998, and 1999, respectively (flux toward the surface is positive), and the associated variation seemed to mirror the severity of moisture stress. We also examined integrated values of NEE during different periods (e.g. day/night; growing season/senescence). Annually integrated carbon dioxide uptake during the daytime showed the greatest variability from year to year, and was primarily linked to the severity of moisture stress. Carbon loss during nighttime was a significant part of the annual daytime NEE, and was fairly stable from year to year. When carbon loss during the burn (estimated from pre‐ and post‐burn biomass samples) was incorporated in the annual NEE, the prairie was found to be approximately carbon neutral (i.e. net carbon uptake/release was near zero) in years with no moisture stress (1997) or with some stress late in the season (1999). During a year with severe moisture stress early in the season (1998), the prairie was a net source of carbon. It appears that moisture stress (severity as well as timing of occurrence) was a dominating factor regulating the annual carbon exchange of the prairie.     

北京八达岭林场人工林净碳交换及其环境影响因子

2011年11月-2012年10月,采用涡度相关法对北京市八达岭林场4年生针阔混交人工林的碳交换特征进行了连续观测.结果表明： 观测期间,该森林生态系统在7、8月为碳汇,其余月份均为碳源,净碳释放量与吸收量分别在4月和7月达到最大.生态系统净生产力为(-256±21) g C·m^-2·a^-1,其中生态系统呼吸为(950±36) g C·m^-2·a^-1,总初级生产力为(694±17) g C·m^-2·a^-1.生态系统呼吸与10 cm深度土壤温度呈较好的指数关系,其温度敏感性系数(Q₁₀)为2.2.在5-9月,白天生态系统净碳交换对光合有效辐射的响应符合直角双曲线方程,表观量子效率呈明显的季节变化(0.0219～0.0506 μmol CO₂·μmol^-1),生态系统最大光合速率和白天平均生态系统呼吸强度与光合有效辐射和温度的季节变化趋势相似.此外,7、8月饱和水汽压差与土壤含水量对白天生态系统净碳交换有显著的影响.
     

黄河三角洲芦苇湿地生长季净生态系统CO2交换及其环境调控机制

采用涡度相关法,对2011年生长季的黄河三角洲芦苇湿地净生态系统CO₂交换(NEE)进行了观测,研究湿地NEE的变化规律及其影响因子.结果表明: 不同月份芦苇湿地的NEE日变化均呈“U”形曲线,CO₂最大净吸收率和释放率的日均值分别为(0.44±0.03)和(0.16±0.01) mg CO₂·m^-2·s^-1;芦苇湿地NEE、生态系统呼吸(R_eco)、总初级生产力(GPP)的季节变化均呈现生长旺季(7—9月)较高、生长初期(5—6月)和生长末期(10—11月)较低的趋势;R_eco和NEE在8月达到峰值,GPP在7月达到峰值.芦苇湿地生态系统的CO₂交换受到光合有效辐射(PAR)、土壤温度(T_s)和土壤体积含水量(SWC)的共同影响.白天NEE与PAR呈直角双曲线关系;5 cm深处T_s与夜间生态系统呼吸(R_eco,n)呈指数关系,生态系统呼吸的温度敏感性(Q₁₀)为2.30,SWC和T_s是影响芦苇湿地R_eco,n的主要因子.在整个生长季,黄河三角洲芦苇湿地生态系统是一个明显的CO₂的汇,总净固碳量为780.95 g CO₂·m^-2.     

Seasonal hysteresis of net ecosystem exchange in response to temperature change: patterns and causes

Understanding how net ecosystem exchange (NEE) changes with temperature is central to the debate on climate change‐carbon cycle feedbacks, but still remains unclear. Here, we used eddy covariance measurements of NEE from 20 FLUXNET sites (203 site‐years of data) in mid‐ and high‐latitude forests to investigate the temperature response of NEE. Years were divided into two half thermal years (increasing temperature in spring and decreasing temperature in autumn) using the maximum daily mean temperature. We observed a parabolic‐like pattern of NEE in response to temperature change in both the spring and autumn half thermal years. However, at similar temperatures, NEE was considerably depressed during the decreasing temperature season as compared with the increasing temperature season, inducing a counter‐clockwise hysteresis pattern in the NEE–temperature relation at most sites. The magnitude of this hysteresis was attributable mostly (68%) to gross primary production (GPP) differences but little (8%) to ecosystem respiration (ER) differences between the two half thermal years. The main environmental factors contributing to the hysteresis responses of NEE and GPP were daily accumulated radiation. Soil water content (SWC) also contributed to the hysteresis response of GPP but only at some sites. Shorter day length, lower light intensity, lower SWC and reduced photosynthetic capacity may all have contributed to the depressed GPP and net carbon uptake during the decreasing temperature seasons. The resultant hysteresis loop is an important indicator of the existence of limiting factors. As such, the role of radiation, LAI and SWC should be considered when modeling the dynamics of carbon cycling in response to temperature change.     

Canopy duration has little influence on annual carbon storage in the deciduous broad leaf forest

Vegetation phenology, the study of the timing and length of the terrestrial growing season and its connection to climate, is increasingly important in integrated Earth system science. Phenological variability is an excellent barometer of short‐ and long‐term climatic variability, strongly influences surface meteorology, and may influence the carbon cycle. Here, using the 1895–1993 Vegetation/Ecosystem Modelling and Analysis dataset and the Biome‐BGC terrestrial ecosystem model, we investigated the relationship between phenological metrics and annual net ecosystem exchange (NEE) of carbon. For the 1167 deciduous broad leaf forest pixels, we found that NEE was extremely weakly related to canopy duration (days from leaf appearance to complete leaf fall). Longer canopy duration, did, however, sequester more carbon if warm season precipitation was above average. Carbon uptake period (number of days with net CO₂ uptake from the atmosphere), which integrates the influence of all ecosystem states and processes, was strongly related to NEE. Results from the Harvard Forest eddy‐covariance site supported our findings. Such dramatically different results from two definitions of ‘growing season length’ highlight the potential for confusion among the many disciplines engaged in phenological research.     

环境和生物因子对黄河三角洲滨海湿地净生态系统CO2交换的影响

通过涡度相关和微气象观测技术,对黄河三角洲滨海湿地净生态系统CO₂交换(NEE)以及环境、生物因子进行了观测,探究湿地NEE变化规律及环境和生物因子对NEE的影响. 结果表明: 在日尺度上,生长季NEE呈明显“U”型曲线,非生长季变幅较小;在季节尺度上,NEE生长季波动较大,表现为碳汇,非生长季波动较小,表现为碳源;在年尺度上,滨海湿地生态系统表现为碳汇,总净固碳量为-247 g C·m^-2. 白天NEE主要受控于光合有效辐射(PAR),且生态系统表观量子产量(α)与白天生态系统呼吸(R_eco,d)均于8月达到最大值,最大光合速率(A_max)于7月达到最大值;夜间NEE随气温(T_a)呈指数增加趋势,生态系统的温度敏感系数(Q₁₀)为2.5,且土壤含水量(SWC)越高,Q₁₀值越大.非生长季NEE只与净辐射(R_n)呈显著的线性负相关,与其他环境因子无显著相关关系.生长季NEE与R_n、T_a、土壤10 cm温度(T_{s 10})等环境因子以及叶面积指数(LAI)呈显著的线性负相关,但与地上生物量(AGB)无显著相关关系.多元回归分析表明,R_n和LAI对生长季NEE的协同影响达到52%.     

环境和生物因子对黄河三角洲滨海湿地净生态系统CO2交换的影响

通过涡度相关和微气象观测技术,对黄河三角洲滨海湿地净生态系统CO₂交换(NEE)以及环境、生物因子进行了观测,探究湿地NEE变化规律及环境和生物因子对NEE的影响. 结果表明: 在日尺度上,生长季NEE呈明显“U”型曲线,非生长季变幅较小;在季节尺度上,NEE生长季波动较大,表现为碳汇,非生长季波动较小,表现为碳源;在年尺度上,滨海湿地生态系统表现为碳汇,总净固碳量为-247 g C·m^-2. 白天NEE主要受控于光合有效辐射(PAR),且生态系统表观量子产量(α)与白天生态系统呼吸(R_eco,d)均于8月达到最大值,最大光合速率(A_max)于7月达到最大值;夜间NEE随气温(T_a)呈指数增加趋势,生态系统的温度敏感系数(Q₁₀)为2.5,且土壤含水量(SWC)越高,Q₁₀值越大.非生长季NEE只与净辐射(R_n)呈显著的线性负相关,与其他环境因子无显著相关关系.生长季NEE与R_n、T_a、土壤10 cm温度(T_{s 10})等环境因子以及叶面积指数(LAI)呈显著的线性负相关,但与地上生物量(AGB)无显著相关关系.多元回归分析表明,R_n和LAI对生长季NEE的协同影响达到52%.