首页 | 本学科首页   官方微博 | 高级检索  
相似文献
 共查询到20条相似文献,搜索用时 656 毫秒
1.
土壤呼吸是陆地生态系统碳收支的重要组成部分。与森林相比,自然或半自然的灌丛主要分布在养分贫瘠的地区,通常认为它们对环境变化较为敏感。外源氮输入可能会显著影响灌丛的土壤呼吸。迄今为止,人们对大气氮沉降对灌丛土壤呼吸的影响知之甚少。该文通过氮添加试验,研究了北京东灵山荆条(Vitex negundo var.heterophylla)和绣线菊(Spiraea salicifolia)灌丛土壤呼吸及其对不同氮添加水平(对照(0)、低氮(20 kg N·hm~(–2)·a~(–1))、中氮(50 kg N·hm~(–2)·a~(–1))和高氮(100 kg N·hm~(–2)·a~(–1)))的响应。结果表明:自然条件下,荆条和绣线菊灌丛的土壤总呼吸年通量为5.91和4.23 t C·hm~(–2)·a~(–1),异养呼吸通量为5.76和3.53 t C·hm~(–2)·a~(–1),荆条和绣线菊灌丛的总呼吸和异养呼吸均与土壤温度呈显著的指数关系。荆条和绣线菊灌丛土壤总呼吸温度敏感性系数(Q_(10))的变化范围分别为1.44–1.58和1.43–1.98,异养呼吸Q10的变化范围分别为1.38–2.11和1.49–1.88。短期氮添加抑制了荆条灌丛的自养呼吸,而对土壤总呼吸和异养呼吸影响不明显;氮添加促进了绣线菊灌丛的异养呼吸,而对土壤总呼吸和自养呼吸均无显著影响;氮添加对两种灌丛土壤呼吸年通量及土壤总呼吸Q10均无显著影响。  相似文献   

2.
日益加剧的氮沉降已经对陆地生态系统生产力和碳循环过程产生了显著影响。草原生态系统近90%的碳储存在土壤中, 明确土壤呼吸及其组分对氮添加的响应对评估大气氮沉降背景下草原生态系统碳平衡和土壤碳库稳定性是非常重要的。以往关于草原土壤呼吸对氮沉降响应的理解多是基于短期(<5年)和低频(每年1-2次)氮添加实验研究, 而关于长期氮添加和不同施氮频率对土壤呼吸及其组分的影响尚缺乏实验证据。该研究基于2008年建立在内蒙古半干旱草原的长期氮添加实验平台, 包括6个氮添加水平和2个施氮频率处理, 通过连续两年(2018-2019年)土壤呼吸及其组分的测定, 发现: 1)氮添加显著降低了土壤总呼吸速率(Rs), 且Rs下降程度随着氮添加量的增加而增强。土壤异养呼吸速率(Rh)的显著下降是Rs下降的主要原因。2)不同氮添加频率并未显著影响土壤呼吸及其组分对氮添加处理的响应。3)长期氮添加造成的土壤酸化降低了土壤微生物活性并改变了微生物群落结构(真菌/细菌比), 进而导致土壤呼吸及其异养组分呈现显著的负响应。以上结果表明, 长期(>10年)氮添加对土壤地下碳循环过程的抑制作用非常明显, 特别是异养呼吸组分的下降会降低土壤有机碳分解速率, 有助于土壤碳库稳定性的维持。同时, 随着氮添加处理时间的延长, 不同施氮频率影响效应的差异减弱, 表明目前长期的低频氮添加实验监测数据可以为评估自然生态系统对大气氮沉降的响应提供较为可靠的参考。  相似文献   

3.
随着全球大气氮沉降的明显增加,将有可能显著影响我国西部地区受氮限制的亚高山森林生态系统。土壤微生物是生态系统的重要组成部分,是土壤物质循环和能量流动的重要参与者。由于生态系统类型、土壤养分、氮沉降背景值等的差异,土壤呼吸和土壤生物量碳氮对施氮的响应存在许多不确定性。而施氮会不会促进亚高山森林生态系统中土壤呼吸和微生物对土壤碳氮的固定?基于此假设,选择了川西60年生的四川红杉(Larix mastersiana)亚高山针叶林为研究对象,通过4个水平的土壤施氮控制试验(CK:0 g m~(-2) a~(-1)、N1:2 g m~(-2)a~(-1)、N2:5 g m~(-2) a~(-1)、N3:10 g m~(-2)a~(-1)),监测了土壤呼吸及土壤微生物生物量碳氮在一个生长季的动态情况。结果表明:施氮对土壤呼吸各指标和土壤微生物碳氮都有极显著的影响,施氮能促进土壤全呼吸、自养呼吸、异养呼吸通量和土壤微生物生物量碳氮的增长,施氮使土壤呼吸通量提高了11%—15%,土壤微生物量碳提高了5%—9%,土壤微生物量氮提高了23%—34%。在中氮水平下(5 g m~(-2) a~(-1))对土壤呼吸的促进最显著。相关分析发现,土壤呼吸与微生物生物量碳氮和微生物代谢商极呈显著正相关,微生物量碳氮与土壤温度呈极显著的正相关,与土壤湿度呈极显著负相关。通过一般线性回归拟合土壤呼吸速率与土壤10 cm温湿度的关系,发现土壤呼吸速率与土壤温度呈极显著的正相关,与土壤湿度极显著负相关(P0.001),中氮水平下土壤温度敏感性系数Q_(10)值(7.10)明显高于对照(4.26)。  相似文献   

4.
本研究比较了青藏高原高寒草甸土壤呼吸速率(Rs)、自养呼吸速率(Ra)和异养呼吸速率(Rh)随施氮梯度的变化,揭示土壤呼吸及其组分变化的主要影响因素,为评价未来氮沉降背景下高寒草甸土壤碳释放提供科学依据。于2014年在四川红原青藏高原高寒草甸建立长期氮素添加平台,采取完全随机区组试验设计,设置0(N0,对照)、2(N2)、4(N4)、8(N8)、16(N16)和32 g N·m-2·a-1(N32)6个水平氮素添加控制实验。于2020年生长季对Rs、Ra和Rh进行监测。结果表明:施氮显著降低了土壤呼吸及其组分(P<0.05),且Ra的下降幅度大于Rh,导致Rh/Rs随施氮水平逐渐上升;不同施氮处理下Ra和Rh与土壤温度均呈显著的指数正相关(P<0.05);施氮降低了Ra的温度敏感性(Q10),但提高了Rh的Q10值;土壤呼吸各组分与土壤湿度的关系均不显著,但土壤温度和土壤湿度双因子模型对Ra和Rh的解释度高于单因素模型。本研究揭示了高寒草甸土壤呼吸及其组分对氮添加的响应特征及机制,可为评...  相似文献   

5.
从2013年12月至2014年11月,通过野外原位试验,对华西雨屏区常绿阔叶林进行了模拟氮沉降和降雨试验,采用LI-8100土壤碳通量分析系统(LI-COR Inc.,USA)测定了对照(CK)、氮沉降(N)、减雨(R)、增雨(W)、氮沉降+减雨(NR)、氮沉降+增雨(NW)6个处理水平的土壤呼吸速率,并通过回归方程分析了温度和湿度与土壤呼吸速率间的关系。结果表明:(1)氮沉降和增雨抑制了常绿阔叶林土壤呼吸速率,减雨促进了常绿阔叶林土壤呼吸速率。(2)减雨使华西雨屏区常绿阔叶林土壤呼吸年通量增加了258 g/m~2,而模拟氮沉降和增雨使华西雨屏区常绿阔叶林土壤呼吸年通量分别减少了321g/m~2和406g/m~2。(3)减雨增加了土壤呼吸的温度敏感性,模拟氮沉降和增雨降低了土壤呼吸的温度敏感性。(4)模拟温度和湿度与土壤呼吸速率间回归方程分析表明,土壤水分对土壤呼吸速率的影响较小。(5)模拟氮沉降和增雨处理减少土壤微生物生物量碳、氮的含量,减雨处理增加了土壤微生物生物量碳、氮的含量。(6)模拟氮沉降和降雨对华西雨屏区土壤CO_2释放的影响未表现出明显的交互作用。  相似文献   

6.
杨文佳  李永夫  姜培坤  周国模  刘娟   《生态学杂志》2015,26(10):2937-2945
利用Li-8100土壤碳通量测量系统,研究了2013年4月—2014年3月浙江临安市毛竹人工林土壤呼吸、异养呼吸和自养呼吸速率的动态变化规律.结果表明:毛竹人工林土壤总呼吸速率、异养呼吸速率和自养呼吸速率均呈现出明显的季节变化特征,最高值出现在7月,最低值出现在1月,年平均值分别为2.93、1.92和1.01 μmol CO2·m-2·s-1.毛竹林土壤总呼吸、异养呼吸和自养呼吸年累积CO2排放量分别为37.25、24.61和12.64 t CO2·hm-2·a-1.土壤呼吸各组分均与土壤5 cm温度呈显著指数相关,土壤总呼吸、异养呼吸和自养呼吸的温度敏感系数Q10值分别为2.05、1.95和2.34.土壤总呼吸速率、异养呼吸速率与土壤水溶性有机碳(WSOC)含量均呈显著相关,而自养呼吸与WSOC无显著相关性;土壤呼吸各组分与土壤含水〖JP2〗量以及微生物生物量碳均无显著相关性.土壤温度是影响毛竹人工林土壤呼吸及其组分季节变化的主要驱动因子,土壤WSOC含量是影响土壤总呼吸和异养呼吸的重要环境因子.  相似文献   

7.
我国酸沉降主要分布区域与杉木人工林主要分布区域重合,石灰添加是改良酸化土壤的有效措施。为探究酸沉降背景下施石灰对土壤呼吸及其温度敏感性的影响,本研究以杉木人工林土壤为对象,在2018年6月一次性添加0、1和5 t·hm-2的氧化钙,于2020年6月开始进行为期一年的原位土壤呼吸速率观测。结果表明:与不施石灰相比,施石灰显著提高了土壤pH值和交换性Ca2+含量,不同石灰施用量之间无显著差异。杉木人工林土壤呼吸及其组分具有明显的季节差异,表现为夏季最高,冬季最低,施石灰未显著改变其季节动态特征。施石灰显著降低了土壤异养呼吸速率,提高了自养呼吸速率,最终导致施石灰对土壤呼吸无显著影响。土壤呼吸月动态变化与温度月动态变化基本保持一致,土壤呼吸与土壤温度呈显著的指数关系,施石灰后土壤呼吸及自养呼吸的温度敏感性(Q10)呈上升趋势,土壤异养呼吸的Q10呈下降趋势。综上,施石灰提高了杉木人工林土壤自养呼吸,显著降低了土壤异养呼吸,这有利于杉木人工林土壤固碳。  相似文献   

8.
增温和刈割对高寒草甸土壤呼吸及其组分的影响   总被引:1,自引:0,他引:1  
蒙程  牛书丽  常文静  全权  曾辉 《生态学报》2020,40(18):6405-6415
评估土壤呼吸及其组分对增温等全球变化的响应对于预测陆地生态系统碳循环至关重要。本研究利用红外线辐射加热器(Infrared heater)装置在青藏高原高寒草甸生态系统设置增温和刈割野外控制实验。通过测定2018年生长季(5—9月)土壤呼吸和异养呼吸,探究增温和刈割对土壤呼吸及其组分的影响。研究结果表明:(1) 单独增温使土壤呼吸显著增加31.65% (P<0.05),异养呼吸显著增加27.12% (P<0.05),土壤自养呼吸没有显著改变(P>0.05);单独刈割对土壤呼吸和自养呼吸没有显著影响(P>0.05),单独刈割刺激异养呼吸增加32.54% (P<0.05);(2) 增温和刈割之间的交互作用对土壤呼吸和异养呼吸没有显著影响(P>0.05),但是对自养呼吸的影响是显著的(P<0.05),土壤呼吸和异养呼吸的季节效应显著(P<0.05);(3)土壤呼吸及其组分与土壤温度均成显著指数关系,与土壤湿度呈显著的正相关关系(P<0.05),处理影响它们的响应敏感性。本研究表明青藏高原东缘高寒草甸土壤碳排放与气候变暖存在正反馈。  相似文献   

9.
氮素类型和剂量对寒温带针叶林土壤N2O排放的影响   总被引:1,自引:0,他引:1  
大气氮沉降输入会增加森林生态系统氮素有效性,进而改变土壤N_2O产生与排放,然而有关不同氮素离子(氧化态NO_3~--N与还原态NH_4~+-N)沉降对土壤N_2O排放的影响知之甚少。以大兴安岭寒温带针叶林为研究对象,构建了3种类型(NH_4Cl、KNO_3、NH_4NO_3)和4个施氮水平(0、10、20、40 kg N hm~(-2)a~(-1))的增氮控制试验,利用流动化学分析仪和静态箱-气相色谱法4次/月测定凋落物层和矿质层土壤无机氮含量、土壤-大气界面N_2O净交换通量以及相关环境因子,分析施氮类型和剂量对土壤氮素有效性、土壤N_2O通量的影响探讨氮素富集条件下土壤N_2O通量的环境驱动机制。结果表明:施氮类型和剂量均显著影响土壤无机氮含量,土壤NH_4~+-N的积累效应显著高于NO_3~--N。施氮一致增加寒温带针叶林土壤N_2O排放,NH_4NO_3促进效应最为明显,增幅为442%-677%,高于全球平均水平(134%)。土壤N_2O通量与土壤温度、凋落物层NH_4~+-N含量正相关,且随着施氮水平增加而增加。结果表明大气氮沉降短期内不会导致寒温带针叶林土壤NO_3~--N大量流失,但会显著促进土壤N_2O的排放。此外,外源性NH_4~+和NO_3~-输入对土壤N_2O排放的促进作用具有协同效应,在未来森林生态系统氮循环和氮平衡研究中应该区分对待。  相似文献   

10.
米槠和杉木人工林土壤呼吸及其组分分析   总被引:4,自引:0,他引:4       下载免费PDF全文
区分森林土壤呼吸组分是了解生态系统碳循环的重要环节。该文以福建省三明市格氏栲自然保护区米槠(Castanopsis carlesii)人工林和邻近的杉木(Cunninghamia lanceolata)人工林为研究对象, 于2012年8月至2013年7月, 采用LI-8100开路式土壤碳通量系统, 通过挖壕沟方法, 测定了土壤呼吸及异养呼吸的速率, 同时测定了5 cm深处的土壤温度和0-12 cm深处的土壤含水量。利用指数模型和双因素模型, 分析土壤呼吸及其组分与土壤温度和土壤含水量的关系, 同时计算了土壤呼吸各组分在土壤呼吸中所占的比例, 并分析了不同森林类型对土壤呼吸及其组分的影响。结果表明: 米槠人工林和杉木人工林土壤呼吸及其组分的季节变化显著, 均呈单峰型曲线, 与5 cm深处的土壤温度呈极显著正相关关系。土壤温度可以分别解释米槠人工林土壤呼吸、自养呼吸和异养呼吸变化的70.3%、73.4%和58.2%, 可以解释杉木人工林土壤呼吸、自养呼吸和异养呼吸变化的77.9%、65.7%和79.2%。土壤呼吸及其组分与土壤含水量没有相关关系。米槠和杉木人工林自养呼吸的年通量分别为4.00和2.18 t C·hm-2·a-1, 占土壤呼吸年通量的32.5%和24.1%; 异养呼吸年通量分别为8.32和6.88 t C·hm-2·a-1, 分别占土壤呼吸年通量的67.5%和75.9%, 米槠人工林土壤呼吸及其组分的年通量都大于杉木人工林。  相似文献   

11.
高寒矮嵩草草甸冬季CO2释放特征   总被引:1,自引:0,他引:1  
吴琴  胡启武  曹广民  李东 《生态学报》2011,31(18):5107-5112
冬季碳排放在高寒草地年内碳平衡中占有重要位置。为探讨高寒草地冬季碳排放特征及温度敏感性,于2003-2005年在中国科学院海北高寒草甸生态系统研究站,利用密闭箱-气相色谱法连续观测了高寒矮嵩草草甸2个冬季的生态系统、土壤呼吸通量特征。结果表明:1)高寒矮嵩草草甸冬季生态系统呼吸、土壤呼吸均具有明显的日变化和季节变化规律,温度是其主要的控制因子,能够解释44%以上的呼吸速率变异。2)冬季生态系统呼吸与土壤呼吸速率在统计上没有显著差异,土壤呼吸占生态系统呼吸的比例高达85%以上。3)2003-2004年冬季生态系统呼吸、土壤呼吸的Q10值分别为1.53,1.38;2004-2005年冬季生态系统呼吸与土壤呼吸的Q10值为1.86,1.68,2个冬季生态系统呼吸的Q10值均高于土壤呼吸。4)未发现高寒矮嵩草草甸冷冬年份的Q10值高于暖冬年份以及冬季的Q10值高于生长季。  相似文献   

12.
降雨对草地土壤呼吸季节变异性的影响   总被引:4,自引:0,他引:4  
王旭  闫玉春  闫瑞瑞  杨桂霞  辛晓平 《生态学报》2013,33(18):5631-5635
利用土壤碳通量自动观测系统(LI-8150)对呼伦贝尔草原在自然降雨条件下的土壤呼吸作用进行了野外定位连续观测,研究结果表明:降雨对土壤呼吸作用存在激发效应和抑制效应,降雨发生后1-2 h内土壤呼吸速率可增加约1倍,当单次或者连续降雨累积量大于7-8 mm,或土壤含水量大于29%-30%时,降雨对土壤呼吸会产生明显的抑制作用。土壤呼吸的激发效应往往体现在次日,表现为次日平均土壤呼吸速率的显著升高;而抑制效应则在当日即可体现出来,表现为观测当日平均土壤呼吸速率的明显下降。土壤呼吸季节变异性与降雨频率和降雨强度密切相关,在降雨量一定的情况下,较低的降雨频率和较高的降雨强度会增加土壤呼吸的变异性。呼伦贝尔草甸草原而言,在生长季土壤平均含水量为16.5%时,土壤呼吸的温度敏感性值(Q10)为2.12;而平均土壤含水量为26%时,Q10值为2.82,明显高于前者,土壤含水量与Q10之间存在正相关关系。降雨导致土壤呼吸的激发效应和抑制效应交替发生,使草地土壤呼吸的季节变异性增加,降雨格局变化必然会对草地碳循环和碳通量特征产生深刻影响。  相似文献   

13.
张富华  胡聃  孙凡  郭振  李元征  王晓琳  马生丽 《生态学报》2014,34(24):7385-7392
与光呼吸不同,光对植物叶片暗呼吸具有明显抑制作用。目前,植物叶片这一生理生态现象很少受到关注,但光抑制呼吸会导致叶片日间碳损失,对植物碳平衡有重要影响。利用Li-6400(Li-Cor,USA)光合仪模拟北京城区夏、秋季增温对月季(Rosa chinensis)叶片暗呼吸及光合参数的影响。结果表明:(1)短期增温处理显著提高了蒸腾速率(Tr),降低了胞间CO2浓度(Ci),夏季增温时气孔导度(Gs)降低而秋季增温明显升高。(2)夏季增温5℃,有光暗呼吸(RL)显著高于增温2℃(P0.05),而增温2℃对RL影响不显著(P0.05);秋季增温5℃,RL显著高于增温3℃(P0.05)。4个不同短期增温处理都对无光暗呼吸(RD)影响显著(P0.05)。(3)秋季增温5℃对光抑制呼吸影响显著(P0.05);其它3个短期增温影响不显著(P0.05)。(4)秋季增温5℃,月季暗呼吸对增温敏感性显著高于增温3℃的值(P0.05)。目的为分析城市白昼气温上升导致植物叶片碳损失估计提供实验案例,是提高城市植物碳汇生态服务功能可能途径的基础。  相似文献   

14.
The fumarate reductases from S. frigidimarina NCIMB400 and S. oneidensis MR-1 are soluble and monomeric enzymes located in the periplasm of these bacteria. These proteins display two redox active domains, one containing four c-type hemes and another containing FAD at the catalytic site. This arrangement of single-electron redox co-factors leading to multiple-electron active sites is widespread in respiratory enzymes. To investigate the properties that allow a chain of single-electron co-factors to sustain the activity of a multi-electron catalytic site, redox titrations followed by NMR and visible spectroscopies were applied to determine the microscopic thermodynamic parameters of the hemes. The results show that the redox behaviour of these fumarate reductases is similar and dominated by a strong interaction between hemes II and III. This interaction facilitates a sequential transfer of two electrons from the heme domain to FAD via heme IV.  相似文献   

15.

Background and Aims

Elucidation of the mechanisms by which plants adapt to elevated CO2 is needed; however, most studies of the mechanisms investigated the response of plants adapted to current atmospheric CO2. The rapid respiration rate of cotton (Gossypium hirsutum) fruits (bolls) produces a concentrated CO2 microenvironment around the bolls and bracts. It has been observed that the intercellular CO2 concentration of a whole fruit (bract and boll) ranges from 500 to 1300 µmol mol−1 depending on the irradiance, even in ambient air. Arguably, this CO2 microenvironment has existed for at least 1·1 million years since the appearance of tetraploid cotton. Therefore, it was hypothesized that the mechanisms by which cotton bracts have adapted to elevated CO2 will indicate how plants will adapt to future increased atmospheric CO2 concentration. Specifically, it is hypothesized that with elevated CO2 the capacity to regenerate ribulose-1,5-bisphosphate (RuBP) will increase relative to RuBP carboxylation.

Methods

To test this hypothesis, the morphological and physiological traits of bracts and leaves of cotton were measured, including stomatal density, gas exchange and protein contents.

Key results

Compared with leaves, bracts showed significantly lower stomatal conductance which resulted in a significantly higher water use efficiency. Both gas exchange and protein content showed a significantly greater RuBP regeneration/RuBP carboxylation capacity ratio (Jmax/Vcmax) in bracts than in leaves.

Conclusions

These results agree with the theoretical prediction that adaptation of photosynthesis to elevated CO2 requires increased RuBP regeneration. Cotton bracts are readily available material for studying adaption to elevated CO2.  相似文献   

16.
Much effort has been expended to improve irrigation efficiency and drought tolerance of agronomic crops; however, a clear understanding of the physiological mechanisms that interact to decrease source strength and drive yield loss has not been attained. To elucidate the underlying mechanisms contributing to inhibition of net carbon assimilation under drought stress, three cultivars of Gossypium hirsutum were grown in the field under contrasting irrigation regimes during the 2012 and 2013 growing season near Camilla, Georgia, USA. Physiological measurements were conducted on three sample dates during each growing season (providing a broad range of plant water status) and included, predawn and midday leaf water potential (ΨPD and ΨMD), gross and net photosynthesis, dark respiration, photorespiration, and chlorophyll a fluorescence. End-of-season lint yield was also determined. ΨPD ranged from −0.31 to −0.95 MPa, and ΨMD ranged from −1.02 to −2.67 MPa, depending upon irrigation regime and sample date. G. hirsutum responded to water deficit by decreasing stomatal conductance, increasing photorespiration, and increasing the ratio of dark respiration to gross photosynthesis, thereby limiting PN and decreasing lint yield (lint yield declines observed during the 2012 growing season only). Conversely, even extreme water deficit, causing a 54% decline in PN, did not negatively affect actual quantum yield, maximum quantum yield, or photosynthetic electron transport. It is concluded that PN is primarily limited in drought-stressed G. hirsutum by decreased stomatal conductance, along with increases in respiratory and photorespiratory carbon losses, not inhibition or down-regulation of electron transport through photosystem II. It is further concluded that ΨPD is a reliable indicator of drought stress and the need for irrigation in field-grown cotton.  相似文献   

17.
The spatial and temporal variations of soil respiration were studied from May 2004 to June 2005 in a C3/C4 mixed grassland of Japan. The linear regression relationship between soil respiration and root biomass was used to determine the contribution of root respiration to soil respiration. The highest soil respiration rate of 11-54 Μmol m-2 s-1 was found in August 2004 and the lowest soil respiration rate of 4.99 Μmol m-2 s-1 was found in April 2005. Within-site variation was smaller than seasonal change in soil respiration. Root biomass varied from 0.71 kg m-2 in August 2004 to 102 in May 2005. Within-site variation in root biomass was larger than seasonal variation. Root respiration rate was highest in August 2004 (5.7 Μmol m-2 s-1) and lowest in October 2004 (1.7 Μmol m-2 s-1). Microbial respiration rate was highest in August 2004 (5.8 Μmol m-2 s-1) and lowest in April 2005 (2.59 Μmol m-2 s-1). We estimated that the contribution of root respiration to soil respiration ranged from 31% in October to 51% in August of 2004, and from 45% to 49% from April to June 2005.  相似文献   

18.
Little is known about the respiratory components of CO2 emitted from soils and attaining a reliable quantification of the contribution of root respiration remains one of the major challenges facing ecosystem research. Resolving this would provide major advances in our ability to predict ecosystem responses to climate change. The merits and technical and theoretical difficulties associated with different approaches adopted for partitioning respiration components are discussed here. The way forward is suggested to be the development of non-invasive regression analysis validated by stable isotope approaches to increase the sensitivity of model functions to include components of rhizosphere microbial activity, changing root biomass and the dynamics of a wide range of soil C pools. Section Editor: A. Hodge  相似文献   

19.
Rapid light curves (RLCs), based on pulse amplitude modulated (PAM) fluorometry, were used to investigate the spatio-temporal variability in photosynthesis versus irradiance parameters (α, Ik and Pmax) and the Fv/Fm ratio of the seagrass Zostera tasmanica (formerly Heterozostera tasmanica). Spatial variation was examined across scales ranging from within a leaf (cms) to across the bed (ms), using a nested analysis of covariance sampling design. Overall, significant variation was identified at all scales examined, excluding the largest scale (area). Patterns of variability differed among individual parameters; however a high percentage of the variation was consistently assigned to the covariates, age (within and between leaves) for all parameters, except Pmax.  相似文献   

20.
The transient electron transfer (ET) interactions between cytochrome c1 of the bc1-complex from Paracoccus denitrificans and its physiological redox partners cytochrome c552 and cytochrome c550 have been characterized functionally by stopped-flow spectroscopy. Two different soluble fragments of cytochrome c1 were generated and used together with a soluble cytochrome c552 module as a model system for interprotein ET reactions. Both c1 fragments lack the membrane anchor; the c1 core fragment (c1CF) consists of only the hydrophilic heme-carrying domain, whereas the c1 acidic fragment (c1AF) additionally contains the acidic domain unique to P. denitrificans. In order to determine the ionic strength dependencies of the ET rate constants, an optimized stopped-flow protocol was developed to overcome problems of spectral overlap, heme autoxidation and the prevalent non-pseudo first order conditions. Cytochrome c1 reveals fast bimolecular rate constants (107 to 108 M− 1 s− 1) for the ET reaction with its physiological substrates c552 and c550, thus approaching the limit of a diffusion-controlled process, with 2 to 3 effective charges of opposite sign contributing to these interactions. No direct involvement of the N-terminal acidic c1-domain in electrostatically attracting its substrates could be detected. However, a slight preference for cytochrome c550 over c552 reacting with cyochrome c1 was found and attributed to the different functions of both cytochromes in the respiratory chain of P. denitrificans.  相似文献   

设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号