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1.
氮水添加对高寒草甸生态系统生产力的影响 降水变化和大气氮沉降增加对草原生态系统碳交换具有重要的影响,进而影响草地生产力、群落组成和生态系统功能。然而,氮水添加对高寒草甸生态系统碳交换的影响目前尚不清楚。因此,本研究在青藏高原高寒草甸布设氮水添加试验,设置4种不同处理:对照、 加氮、加水和同时添加氮水,对生态系统碳交换过程进行了连续4年的原位观测。研究结果发现,氮添加可以增加总生态系统生产力(GEP)、植物地上生物量、群落盖度和群落加权平均高度(CWMh),而水分添加没有显著影响。生态系统碳交换对氮水添加的响应在干湿年存在显著差异。水分添加仅在干旱年对净生态系统碳交换(NEE)具有显著影响,原因是GEP的增加量大于生态系统呼吸(ER)。相反,氮添加仅在湿润年显著提高了生态系统碳交换,其中GEP的增加归因于NEE的增加量大于ER。结构方程结果表明,氮添加主要通过增加优势种的盖度从而提高NEE。本研究强调了降水和优势物种在调节高寒草甸生态系统响应环境变化中的重要作用。  相似文献   

2.
基于Biome-BGC模型的西双版纳橡胶林碳收支模拟   总被引:1,自引:0,他引:1  
以西双版纳橡胶适宜种植区(海拔550—600m)的橡胶林(Hevea brasiliensis)为研究对象,应用参数同化后的Biome-BGC模型模拟了1959—2012年橡胶林的碳循环。结果表明,(1)与涡度相关监测结果相比,橡胶林年总初级生产力(Gross Primary Productivity,GPP)、年总呼吸(Total Respiration,Rt)的模拟精度分别为98.37%和90%。由于对年GPP的过低估计和对年Rt的过高估计,年净生态系统交换量(Net Ecosystem Exchange,NEE)的模拟值比实测值低157.35 g C m~(-2)a~(-1)。但若考虑干胶碳(139g C m~(-2)a~(-1)),模拟值与实测值十分接近;(2)橡胶林在模拟进行的前8年里因异养呼吸较高,以碳排放为主,NEE平均约357 g C m~(-2)a~(-1);之后转为以碳固定为主,NEE平均约~(-1)46 g C m~(-2)a~(-1);(3)橡胶林在40年的更新周期中可固定碳1835 g C m~(-2),是一个弱的碳汇。但与热带雨林相同周期固碳6720 g C m~(-2)相比,仍为碳源。以上结果为深入了解橡胶种植对区域碳循环的影响提供了科学依据,建议当地政府一方面要有计划的对老胶林进行更新,以维持当前橡胶林生态系统中的碳平衡;另一方面要注重对热带雨林的保护,从而实现区域经济和生态环境保护的协调发展。  相似文献   

3.
气候变暖和大气氮沉降是全球变化的重要驱动因子。在草地生态系统中,气温升高和大气氮沉降都会改变草地固碳(C)状况,然而温度增加和大气氮沉降是如何影响生态系统碳交换目前还不明确。本研究旨在研究增温和氮素添加对荒漠草原碳交换的影响。在短花针茅荒漠草原上采用2×2因素完全随机区组的裂区设计,使用红外辐射器来模拟气候变暖并且使用添加氮肥的方法来模拟大气氮沉降,在不同处理条件下测定生态系统净碳交换(NEE)、生态系统呼吸(ER)和总生态系统生产力(GEP),分析了2013和2014年影响短花针茅荒漠草原生态系统C交换的因素,结果如下:(1)增温使土壤温度显著增加了0.70℃(P0.001),土壤湿度显著增加了7.58%(P0.001)。(2)增温、氮素添加及其交互作用显著增加了GEP和ER(P0.05),而对于NEE没有显著影响(P0.05)。(3)2013年GEP在8月初达到峰值,ER在8月末9月初达到峰值,NEE随着GEP和ER的变化而波动;2014年GEP、ER和NEE均在8月末9月初达到峰值。(4)ER和GEP随着大气温度升高和降水增加而增大,土壤温度和土壤湿度也是影响生态系统C交换的重要因素。  相似文献   

4.
增温对青藏高原高寒草原生态系统碳交换的影响   总被引:1,自引:0,他引:1  
碳交换是影响草地生态系统碳汇功能的关键过程,对气候变暖极为敏感。青藏高原分布着大面积的高寒草原,其碳汇功能对气候变暖的响应对区域碳循环过程具有重要的影响。为探究高寒草原生态系统碳交换过程对增温的响应,2012—2014年,在青藏高原班戈县进行了模拟增温对高寒草原生态系统碳交换过程影响的研究。结果表明,增温对高寒草原碳交换各组分的影响存在年际差异,但总体上对碳交换存在负面影响。3年平均结果显示,增温显著降低了高寒草原地上生物量、总生态系统生产力(GEP)、生态系统呼吸(ER)和净生态系统碳交换量(NEE)(P0.05),平均降幅分别为15.1%、36.8%、19.2%和51.5%。增温条件下3年平均土壤呼吸(SR)较对照无显著变化(P0.05),但2013年增温显著降低了SR(P0.05),降幅达18.1%。增温对SR与ER的比值具有一定的促进作用,最高增幅达到40.0%。GEP、ER、SR和NEE与土壤温度和土壤水分无显著相关(P0.05),而GEP、ER和NEE与空气温度呈显著的负相关关系(P0.05)。增温引起的干旱胁迫以及地上生物量降低是导致高寒草原NEE降低的主要原因。研究表明,全球变暖会一定程度降低青藏高原高寒草原的碳汇功能。  相似文献   

5.
朱湾湾  许艺馨  余海龙  王攀  黄菊莹 《生态学报》2021,41(16):6679-6691
为深入了解降水格局改变和氮沉降增加对荒漠草原生态系统碳交换的影响机制,于2017年在宁夏荒漠草原设立了降水量变化(减少50%、减少30%、自然降水量、增加30%以及增加50%)和氮添加(0和5 g m-2 a-1)的野外试验,研究了2019年生长季(5-10月份)净生态系统碳交换(Net ecosystem carbon exchange,NEE)、生态系统呼吸(Ecosystem respiration,ER)和总生态系统生产力(Gross ecosystem productivity,GEP)的时间动态,分析了三者与植被组成以及土壤属性的关系。NEE、ER和GEP日动态和月动态均呈先增加后降低,NEE在整个生长季表现为净生态系统碳吸收。0和5 g m-2 a-1氮添加下,减少降水量显著降低了NEE、ER和GEP (P<0.05),增加30%降水量显著提高了三者(P<0.05)。相同降水量条件下,氮添加不同程度地提高了NEE、ER和GEP,且其效应在增加50%降水量时较为明显。净生态系统碳吸收(-NEE)、ER和GEP与群落生物量、牛枝子(Lespedeza potaninii)以及草木樨状黄芪(Astragalus melilotoides)生物量正相关。三者亦随Patrick丰富度指数和Shannon-Wiener多样性指数的增加而增加。本文结果意味着,减少降水量降低了土壤水分和养分有效性、抑制了植物生长,从而降低了生态系统碳交换。适量增加降水量则可能通过提高土壤含水量、刺激土壤酶活性、调节土壤C : N : P平衡特征等途径,促进了植物生长和物种多样性,从而提高了生态系统碳汇功能;氮添加亦促进了生态系统碳交换,但其与降水的交互作用尚不明显,需通过长期观测进行深入探讨。  相似文献   

6.
以科尔沁沙质草地为研究对象,利用开路涡度相关系统和LI-8150土壤呼吸自动观测系统,分析了生长季生态系统二氧化碳(CO_2)净交换量(NEE)的变化特征,土壤呼吸(R_s)对生态系统呼吸(R_(eco))的贡献率,以及生态系统总初级生产力(GPP)的大小。结果表明:生长季NEE存在明显的月均日变化特征,总体呈单峰型,其中7月的日变化最为明显,NEE月均日最大吸收速率(-5.62μmol·m~(-2)·s~(-1))和最大释放速率(3.14μmol·m~(-2)·s~(-1))均出现在7月份;生长季内生态系统总体表现为碳汇,固碳量为25.85 g C·m~(-2);R_s对R_(eco)的贡献率为78.39%,R_(eco)对GPP的贡献率为90.62%,生长季内GPP总累积量为275.51g C·m~(-2)。  相似文献   

7.
为明确围栏封育对斑块化退化高寒草甸净生态系统碳交换(NEE)不同组分的影响,本研究选取青藏高原黄河源区斑块化退化高寒草甸进行围封试验,设置4个围封年限(1、2、5、11 a)和1个正常放牧对照,研究NEE及组分对不同围封年限的响应。结果表明,围封5 a退化高寒草甸总初级生产力(GPP)和生态系统呼吸(ER)显著大于正常放牧、围封1 a、2 a和11 a,围封2 a和5 a退化高寒草甸NEE显著小于正常放牧、围封1 a和11 a样地(P<0.01),其他NEE组分对不同围封年限的响应情况不一致。植被自养呼吸(Ra)、根系呼吸(Rr)和土壤异养呼吸(Rh)占ER的比例在不同围封年限间差异显著(P<0.01)。此外,土壤温度与NEE呈二次曲线的关系,与ER以及除Rh以外的其他呼吸组分呈指数关系,土壤含水量与NEE、GPP、ER、土壤呼吸(Rs)、Ra、Rr呈线性关系(P<0.05)。全氮、全磷、生物量和NEE及组分存在显著的相关关系。说明围封5 a能显著提高退化草地的土壤养分和固碳功能,并能维持草地生产力,无需进行长期围封。  相似文献   

8.
草地生态系统是我国最大的陆地生态系统, 其碳循环的动态变化在全球碳收支平衡中扮演着重要角色。放牧是草地生态系统的主要利用方式。不同的放牧利用强度对草地生态系统会产生不同的影响。该文采用便携式光合仪LI-6400和密闭式箱法于2014-2016年生长季(5-10月)测定了3个载畜率处理(对照、轻度放牧和重度放牧)的生态系统净碳交换, 同步测定了土壤10 cm温度和湿度, 探讨载畜率、水热因素对短花针茅(Stipa breviflora)荒漠草原碳交换的影响。结果表明: 载畜率对生态系统净碳交换有显著影响, 随着载畜率的增加, 生态系统净碳交换、生态系统呼吸以及生态系统总初级生产力分别降低了48.6%、35.3%、40.4%。重度放牧显著降低了草地的固碳能力, 但轻度放牧对草地的固碳能力没有显著影响。年际间生态系统净碳交换主要受降水调控。整个生长季, 短花针茅荒漠草原均表现为碳吸收, 土壤温度对生态系统净碳交换的贡献率高于土壤湿度。  相似文献   

9.
《植物生态学报》2018,42(3):361
草地生态系统是我国最大的陆地生态系统, 其碳循环的动态变化在全球碳收支平衡中扮演着重要角色。放牧是草地生态系统的主要利用方式。不同的放牧利用强度对草地生态系统会产生不同的影响。该文采用便携式光合仪LI-6400和密闭式箱法于2014-2016年生长季(5-10月)测定了3个载畜率处理(对照、轻度放牧和重度放牧)的生态系统净碳交换, 同步测定了土壤10 cm温度和湿度, 探讨载畜率、水热因素对短花针茅(Stipa breviflora)荒漠草原碳交换的影响。结果表明: 载畜率对生态系统净碳交换有显著影响, 随着载畜率的增加, 生态系统净碳交换、生态系统呼吸以及生态系统总初级生产力分别降低了48.6%、35.3%、40.4%。重度放牧显著降低了草地的固碳能力, 但轻度放牧对草地的固碳能力没有显著影响。年际间生态系统净碳交换主要受降水调控。整个生长季, 短花针茅荒漠草原均表现为碳吸收, 土壤温度对生态系统净碳交换的贡献率高于土壤湿度。  相似文献   

10.
吕富成  马建勇  曹云  延晓冬 《生态学报》2022,42(7):2810-2821
森林生态系统是陆地碳循环的重要组成部分,其固碳能力显著高于其他陆地生态系统,研究森林生态系统碳通量是认识和理解全球变化对碳循环影响的关键。碳循环模型是研究森林生态系统碳通量有效工具。以长白山温带落叶阔叶林、千烟洲亚热带常绿针叶林、鼎湖山亚热带常绿阔叶林和西双版纳热带雨林等4种中国典型森林生态系统为研究对象,利用涡度相关2003-2012年观测数据,评估FORCCHN模型对生态系统呼吸(ER),总初级生产力(GPP),净生态系统生产力(NEP)的模型效果。结果表明:(1) FORCCHN模型能够较好的模拟中国4种典型森林生态系统不同时间尺度的碳通量。落叶阔叶林和常绿针叶林ER和GPP的逐日变化模拟效果较好(ER的相关系数分别为0.94和0.92,GPP的相关系数分别为0.86和0.74);(2)4种森林生态系统碳通量季节动态模拟值和观测值显著相关(P<0.01),ER、GPP、NEP的观测值和模拟值的R2分别为0.77-0.93、0.54-0.88和0.15-0.38;模型可以很好地模拟森林生态系统不同季节碳汇(NEP>0),碳源(NEP<0)的变化规律;(3)4种森林生态系统碳通量模拟值与观测值的年际变化有很好的吻合度,但在数值大小上存在差异,模型高估了常绿阔叶林的ER和GPP,略微低估了其他3种森林生态系统ER和GPP。  相似文献   

11.
太湖流域典型稻麦轮作农田生态系统碳交换及影响因素   总被引:4,自引:0,他引:4  
徐昔保  杨桂山  孙小祥 《生态学报》2015,35(20):6655-6665
利用涡度相关技术观测太湖流域典型稻麦轮作农田生态系统2a净生态系统碳交换(NEE)变化过程,分析其碳交换特征及影响机理,结果表明:太湖流域典型稻麦轮作农田年NEE为-749.49—-785.38 g C m-2a-1,考虑作物籽粒碳和秸秆还田后净吸收88.12 g C m-2a-1,为弱碳汇;稻/麦季日均NEE和白天NEE季节变化直接受作物植被生长影响;麦季夜间NEE与10 cm土壤温度呈显著指数关系,2012/2013年温度敏感系数(Q10)分别为3.03和2.67;当土壤水分低于田间持水量时,麦季夜间NEE主要受土壤温度影响,反之,夜间NEE受土壤温度和水分双重影响;降水对麦季夜间NEE有短时的激发效应;稻季淹水对土壤呼吸产生较明显的阻滞效应,降低了夜间NEE对土壤温度的敏感性,2012和2013年分别为1.88和1.39,稻季淹水与烤田交替变化对土壤呼吸产生明显的抑制或激发的短时效应。  相似文献   

12.
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   

13.
Switchgrass (Panicum virgatum L.) has gained importance as feedstock for bioenergy over the last decades due to its high productivity for up to 20 years, low input requirements, and potential for carbon sequestration. However, data on the dynamics of CO2 exchange of mature switchgrass stands (>5 years) are limited. The objective of this study was to determine net ecosystem exchange (NEE), ecosystem respiration (Re), and gross primary production (GPP) for a commercially managed switchgrass field in its sixth (2012) and seventh (2013) year in southern Ontario, Canada, using the eddy covariance method. Average NEE flux over two growing seasons (emergence to harvest) was ?10.4 μmol m?2 s?1 and reached a maximum uptake of ?42.4 μmol m?2 s?1. Total annual NEE was ?380 ± 25 and ?430 ± 30 g C m?2 in 2012 and 2013, respectively. GPP reached ?1354 ± 23 g C m?2 in 2012 and ?1430 ± 50g C m?2 in 2013. Annual Re in 2012 was 974 ± 20 g C m?2 and 1000 ± 35 g C m?2 in 2013. GPP during the dry year of 2012 was significantly lower than that during the normal year of 2013, but yield was significantly higher in 2012 with 1090 g  m?2, compared to 790 g m?2 in 2013. If considering the carbon removed at harvest, the net ecosystem carbon balance came to 106 ± 45 g C  m?2 in 2012, indicating a source of carbon, and to ?59 ± 45 g C m?2 in 2013, indicating a sink of carbon. Our results confirm that switchgrass can switch between being a sink and a source of carbon on an annual basis. More studies are needed which investigate this interannual variability of the carbon budget of mature switchgrass stands.  相似文献   

14.
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   

15.
Eddy‐covariance measurements of net ecosystem carbon exchange (NEE) were carried out above a grazed Mediterranean C3/C4 grassland in southern Portugal, during two hydrological years, 2004–2005 and 2005–2006, of contrasting rainfall. Here, we examine the seasonal and interannual variation in NEE and its major components, gross primary production (GPP) and ecosystem respiration (Reco), in terms of the relevant biophysical controls. The first hydrological year was dry, with total precipitation 45% below the long‐term mean (669 mm) and the second was normal, with total precipitation only 12% above the long‐term mean. The drought conditions during the winter and early spring of the dry year limited grass production and the leaf area index (LAI) was very low. Hence, during the peak of the growth period, the maximum daily rate of NEE and the light‐use and water‐use efficiencies were approximately half of those observed in the normal year. In the summer of 2006, the warm‐season C4 grass, Cynodon dactylon L., exerted an evident positive effect on NEE by converting the ecosystem into a carbon sink after strong rain events and extending the carbon sequestration for several days, after the end of senescence of the C3 grasses. On an annual basis, the GPP and NEE were 524 and 49 g C m?2, respectively, for the dry year, and 1261 and ?190 g C m?2 for the normal year. Therefore, the grassland was a moderate net source of carbon to the atmosphere, in the dry year, and a considerable net carbon sink, in the normal year. In these 2 years of experiment the total amount of precipitation was the main factor determining the interannual variation in NEE. In terms of relevant controls, GPP and NEE were strongly related to incident photosynthetic photon flux density on short‐term time scales. Changes in LAI explained 84% and 77% of the variation found in GPP and NEE, respectively. Variations in Reco were mainly controlled by canopy photosynthesis. After each grazing event, the reduction in LAI affected negatively the NEE.  相似文献   

16.

Background

Increasing atmospheric CO2 and nitrogen (N) deposition across the globe may affect ecosystem CO2 exchanges and ecosystem carbon cycles. Additionally, it remains unknown how increased N deposition and N addition will alter the effects of elevated CO2 on wetland ecosystem carbon fluxes.

Methodology/Principal Findings

Beginning in 2010, a paired, nested manipulative experimental design was used in a temperate wetland of northeastern China. The primary factor was elevated CO2, accomplished using Open Top Chambers, and N supplied as NH4NO3 was the secondary factor. Gross primary productivity (GPP) was higher than ecosystem respiration (ER), leading to net carbon uptake (measured by net ecosystem CO2 exchange, or NEE) in all four treatments over the growing season. However, their magnitude had interannual variations, which coincided with air temperature in the early growing season, with the soil temperature and with the vegetation cover. Elevated CO2 significantly enhanced GPP and ER but overall reduced NEE because the stimulation caused by the elevated CO2 had a greater impact on ER than on GPP. The addition of N stimulated ecosystem C fluxes in both years and ameliorated the negative impact of elevated CO2 on NEE.

Conclusion/Significance

In this ecosystem, future elevated CO2 may favor carbon sequestration when coupled with increasing nitrogen deposition.  相似文献   

17.
川西贡嘎山峨眉冷杉成熟林生态系统CO2通量特征   总被引:1,自引:0,他引:1  
张元媛  朱万泽  孙向阳  胡兆永 《生态学报》2018,38(17):6125-6135
成熟森林的碳收支对陆地生态系统碳循环研究具有重要意义。目前,我国关于西南亚高山暗针叶林成熟林碳通量的研究还相对较少,尚不明确对碳循环的作用。以涡度相关技术为基础,对川西贡嘎山东坡峨眉冷杉成熟林生态系统尺度的CO_2通量进行长期定位观测。利用2015年6月至2016年5月观测数据,分析了峨眉冷杉成熟林净生态系统CO_2交换量(NEE)、生态系统呼吸(Re)和总生态系统生产力(GPP)的季节变异特征及其源汇状况,并结合环境因子,分析CO_2通量的主要控制因子。结果表明:(1)峨眉冷杉成熟林NEE具有明显的日变化特征,呈现"U"形变化,白天为负值,夜间为正值,中午前后CO_2通量达到最大;各月间日平均NEE变化差异显著,NEE峰值最大出现在2015年6月(-0.64 mg CO_2m~(-2)s~(-1)),峰值最小出现在2016年1月(-0.08 mg CO_2m~(-2)s~(-1));日平均NEE由正值变为负值的时间夏季最早,冬季最晚,NEE由负值变为正值的时间冬季最早,夏季最晚。(2)峨眉冷杉成熟林NEE、Re和GPP具有明显的月变化。2015年6月和12月NEE分别达到最大值(-46.02 g C m~(-2)月~(-1))和最小值(-1.42 g C m~(-2)月~(-1));Re呈现单峰变化,最大和最小值分别出现在2015年6月(84.78 g C m~(-2)月~(-1))和2016年1月(12.82 g C m~(-2)月~(-1));GPP最大值和最小值分别出现在2015年6月(130.81 g C m~(-2)月~(-1))与2016年1月(16.15 g C m~(-2)月~(-1))。(3)空气温度(T_a)、5 cm土壤温度(T_(s5))和光合有效辐射(PAR)是影响峨眉冷杉成熟林CO_2通量的主要环境因子。T_a与CO_2通量呈指数相关(R~2=0.5283,P0.01);白天CO_2通量与PAR显著相关(R~2=0.4373,P0.01);夜晚CO_2通量与T_(s5)显著相关(R~2=0.4717,P0.01)。(4)全年NEE、Re和GPP分别为-241.87、564.81 g C m~(-2)和806.68 g C m~(-2),表明川西贡嘎山峨眉冷杉成熟林具有较强的碳汇功能。  相似文献   

18.
Tea plantations are widely distributed and continuously expanding across subtropical China in recent years. However, carbon flux exchanges from tea plantation ecosystems are poorly understood at the ecosystem level. In this study, we use the eddy covariance technique to quantify the magnitude and temporal variations of the net ecosystem exchange (NEE) in tea plantation in Southeast China over four years (2014–2017). The result showed that the tea plantation was a net carbon sink, with an annual NEE that ranged from ?182.40 to ?301.51 g C/m2, which was a much lower carbon sequestration potential than other ecosystems in subtropical China. Photosynthetic photon flux density (PPFD) explained the highest proportion of the variation in NEE and gross primary productivity (GPP) (for NEE: F = 389.89, p < .01; for GPP: F = 1,018.04, p < .01), and air temperature (Ta) explained the highest proportion of the variation in ecosystem respiration (RE) (F = 13,141.81, p < .01). The strong pruning activity in April not only reduced the carbon absorption capacity but also provided many plant residues for respiration, which switched the tea plantation to a carbon source from April to June. Suppression of NEE at higher air temperatures was due to the decrease in GPP more than the decrease in RE, which indicated that future global warming may transform this subtropical tea plantation from a carbon sink to carbon source.  相似文献   

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