城市住宅区碳源汇的空间分异规律、影响机制及管理对策——以关中地区为例

城市住宅区作为城市生态系统重要的组成单元,其碳源汇对城市生态系统碳循环和碳平衡产生重要影响.本文采取案例分析、文献查阅、问卷调查等多种方法,获取关中地区城市住宅区CO₂排放(碳源)与吸收(碳汇)数据,并分析其来源及空间分布情况.结果表明: 关中地区住宅区建材生产和改造更新过程CO₂排放量最大;且建材类的CO₂排放量远大于日常生活资料,仅有40%～52%碳排放发生在住宅区,其余发生在外围,呈现出碳源距离的空间波动性、成分的空间差异性以及圈层与分区分布.仅有9%～17%的碳排放可在住宅区内被吸收,外部空间被动承担大量碳汇功能,并显现为分层递变和空间分异.最后提出了碳源、碳汇空间管理技术和干预对策.
     

基于稳定碳同位素技术研究大气CO2浓度升高对植物-土壤系统碳循环的影响

大气CO₂浓度升高影响植物光合作用过程和生物量积累,改变植物地上和地下生物量的动态分配.土壤有机质的形成和周转依赖于植物组分的输入,因此,CO₂浓度升高所造成的植物生理和代谢的变化对土壤碳库收支平衡具有重要影响.采用稳定碳同位素(¹³C)技术研究土壤-植物系统的碳循环可阐明大气CO₂浓度升高条件下光合碳在植物各器官的分配特征和时间动态,明确光合碳在土壤中的积累、分解与迁移转化过程以及对土壤有机碳库周转的影响.本文综述了基于¹³C自然丰度法或¹³C示踪技术研究大气CO₂浓度升高对土壤-植物系统碳循环的影响,主要包括:1)对植物光合作用的同位素分馏的影响;2)对植物光合碳(新碳)分配动态的影响;3)对土壤有机碳新老碳库动态以及微生物转化过程的影响.明确上述过程及其调控机制可为预测CO₂浓度升高对陆地生态系统碳循环及源汇效应的长期影响奠定基础.     

基于稳定碳同位素技术研究大气CO2浓度升高对植物-土壤系统碳循环的影响

大气CO₂浓度升高影响植物光合作用过程和生物量积累,改变植物地上和地下生物量的动态分配.土壤有机质的形成和周转依赖于植物组分的输入,因此,CO₂浓度升高所造成的植物生理和代谢的变化对土壤碳库收支平衡具有重要影响.采用稳定碳同位素(¹³C)技术研究土壤-植物系统的碳循环可阐明大气CO₂浓度升高条件下光合碳在植物各器官的分配特征和时间动态,明确光合碳在土壤中的积累、分解与迁移转化过程以及对土壤有机碳库周转的影响.本文综述了基于¹³C自然丰度法或¹³C示踪技术研究大气CO₂浓度升高对土壤-植物系统碳循环的影响,主要包括:1)对植物光合作用的同位素分馏的影响;2)对植物光合碳(新碳)分配动态的影响;3)对土壤有机碳新老碳库动态以及微生物转化过程的影响.明确上述过程及其调控机制可为预测CO₂浓度升高对陆地生态系统碳循环及源汇效应的长期影响奠定基础.     

科尔沁沙地流动沙丘不同时空尺度水热变化及CO2交换特征

陆面碳循环在气候变化和生态系统碳收支平衡中起到关键作用。水热变化与CO₂交换分析对于深刻揭示荒漠生态系统的区域碳循环规律及机制具有重要意义。本研究选取科尔沁沙地典型流动沙丘为对象,利用涡度相关技术和波文比气象观测系统所测的数据分析近地层水热变化及CO₂交换特征,探讨了日和季节尺度,以及0～10 m垂直空间尺度下流动沙丘近地层温湿度与CO₂交换过程的相互关系。结果表明: 研究区近地表气温垂直变幅在0.4～2 ℃,4—9月,气温随着高度的升高呈减的趋势,其余月份则相反,空气相对湿度季节变幅超过40%;在2018年生长季,沙丘净生态系统碳交换量(NEE)的日均值为-0.02 mg·m^-2·s^-1,全年水平的NEE日均值为0.003 mg·m^-2·s^-1,全年整体上表现为碳源;垂直空间尺度上,垂直温、湿度差与NEE拟合均较好,水热影响拐点分别为10%和0.5 ℃,而全年尺度上温度拟合结果相对较好,水热影响拐点分别为17 ℃和65%。在生长季,研究区近地层垂直温差为负,会抑制流动沙丘对大气CO₂的吸收,而大气高湿环境则会促进流动沙丘对大气CO₂的吸收。不同时间和不同垂直高度上,水热变化与CO₂交换关系较密切,对沙丘碳汇和碳源的产生具有一定的影响,且碳收支对温度的敏感性强于相对湿度。     

华北平原冬小麦农田生态系统CO2通量特征及其影响因素

利用2014—2015年中国科学院封丘农业生态实验站涡度相关系统观测的冬小麦农田生态系统CO₂通量数据,结合试验地常规气象观测系统的气象数据,分析冬小麦4个生育期(分蘖期、越冬期、拔节期和灌浆期)内CO₂通量的日变化,研究净生态系统碳交换(NEE)的季节变化及其与气象要素的关系.结果表明: 冬小麦整个生育期内NEE为-360.15 g C·m^-2,总初级生产力总量为1920.01 g C·m^-2,冬小麦农田生态系统具有较强的固碳能力.冬小麦农田生态系统CO₂通量具有明显的日变化和季节变化特征,分蘖期表现为碳源,越冬期、拔节期和灌浆期表现为碳汇.表观初始光能利用率平均值为0.03 mg CO₂·μmol^-1,光饱和时的生态系统生产量平均值为1.53 mg CO₂·m^-2·s^-1,月平均生态系统呼吸为193.92 g C·m^-2·month^-1.冬小麦农田生态系统4个生育期NEE与光合有效辐射的相关关系均达到极显著水平.分蘖期、拔节期和灌浆期NEE与饱和水汽压差的相关关系极显著,越冬期达显著水平.冬小麦分蘖期、越冬期和灌浆期NEE日总量与土壤温度呈正相关,拔节期呈负相关关系.     

开垦对黄河三角洲湿地净生态系统CO2交换的影响

近年来, 由于对湿地的不合理利用, 自然湿地被大面积地垦殖为农田, 导致湿地生态系统碳循环的模式发生改变, 从而影响了湿地生态系统碳汇功能。该研究通过涡度相关法, 对山东省东营市黄河三角洲芦苇(Phragmites australis)湿地和开垦多年的棉花(Gossypium spp.)农田的净生态系统CO₂交换(NEE)进行了对比观测, 以探讨该地区典型生态系统NEE的变化规律及其影响因子, 揭示开垦对芦苇湿地NEE和碳汇功能的影响。结果表明: 在生长季, 湿地和农田生态系统NEE的日平均值各月均呈明显的“U”型变化曲线, 非生长季NEE的变幅很小。生长季湿地生态系统日最大净吸收值和释放值分别为16.04 g CO₂·m^-2·d^-1(8月17日)和14.95 g CO₂·m^-2·d^-1(8月9日); 农田生态系统日最大净吸收值和释放值分别为18.99 g CO₂·m^-2·d^-1 (8月22日)和12.23 g CO₂·m^-2·d^-1 (7月29日)。生长季白天两个生态系统NEE与光合有效辐射(PAR)之间呈直角双曲线关系; 非生长季NEE主要受土壤温度(T_s)的影响; 生态系统生长季夜间NEE受T_s和土壤含水量(SWC)的共同影响; 湿地和农田的生态系统呼吸熵(Q₁₀)分别为2.30和3.78。2011年生长季, 黄河三角洲湿地和农田生态系统均表现为CO₂的汇, 总净固碳量分别为780.95和647.35 g CO₂·m^-2, 开垦降低了湿地的碳吸收能力; 而在2011年非生长季, 黄河三角洲湿地和农田生态系统均表现为CO₂的源, CO₂总释放量分别为181.90和111.55 g CO₂·m^-2。全年湿地和农田生态系统总净固碳量分别为599.05和535.80 g CO₂·m^-2。     

红壤和风沙土添加不同化学结构有机碳对外源碳去向及累积贡献的影响

植物凋落物碳输入显著影响陆地生态系统土壤CO₂排放和有机碳(SOC)形成,然而,针对不同质地土壤添加不同化学结构外源碳去向依然不清楚。本研究将¹³C标记的葡萄糖、淀粉和纤维素添加至红壤和风沙土,比较2种质地土壤添加不同化学结构外源碳在土壤释放的CO₂、SOC、可溶性有机碳(DOC)和微生物生物量碳(MBC)库的净累积量、回收率及贡献比例上的差异。结果表明: 添加外源有机碳显著提高了CO₂、SOC、DOC和MBC的δ¹³C值,且随着外源有机碳化学结构复杂性的增加,CO₂的δ¹³C峰值依次延迟出现;外源有机碳种类、土壤类型和培养时间均显著改变外源碳去向及其在各碳库的贡献比例;在风沙土中,外源有机碳更多被矿化为CO₂,且CO₂库的外源碳净累积量和回收率大小依次为葡萄糖>淀粉>纤维素;红壤添加外源碳转变为SOC的累积量和回收率显著高于风沙土,且红壤SOC库的外源碳净累积量和回收率大小顺序也为葡萄糖>淀粉>纤维素。可见,外源有机碳化学结构和土壤质地共同调控外源碳去向及累积贡献。     

不同降雨量年份鄂尔多斯高原油蒿灌丛生态系统碳交换特征

采用涡度相关技术对欠雨年(2011年)和丰雨年(2012年)鄂尔多斯高原油蒿灌丛生态系统CO₂交换量特征及其影响因子进行研究.结果表明: 在两个不同降雨量年份,油蒿灌丛生态系统CO₂交换量日动态根据CO₂吸收峰值的出现分为两种模式,即单峰型和双峰型;2011年生长季内CO₂通量共出现3个明显的吸收峰值和3个释放峰值,2012年生长季内CO₂交换量出现4个吸收峰值和1个释放峰值;2011年6-9月,油蒿灌丛生态系统表现为弱的碳汇,10月转变为碳源;2012年整个生长季,油蒿灌丛生态系统均呈现为碳汇.丰雨年比欠雨年生长季的油蒿灌丛生态系统固碳量增加了268.90 mg CO₂·m^-2·s^-1;在日尺度上,生态系统CO₂交换量受光合有效辐射的控制,在生长季尺度上,非生物因素(降雨量、土壤含水量)和生物因素(生态系统净初级生产力)共同制约油蒿灌丛生态系统CO₂交换量的变化.     

山东省暖性草丛生态系统碳库现状和碳通量季节变化特征

了解山东省草地生态系统碳库现状和碳通量变化规律对于全国尺度草地生态系统碳源/汇核算有着重要的意义。该研究采用野外面上调查取样和固定加强点静态箱法(LI-840红外分析仪联用)相结合的方法, 分析了山东省暖性草丛生态系统的固碳现状、碳通量季节动态以及净生态系统CO₂交换(NEE)对各种环境因子的响应。研究结果表明: 山东暖性草丛生态系统平均碳密度为2.74 Mg C·hm ^-2, 碳密度的构成排序为土壤碳密度(89%) >生物量碳密度(9%) >凋落物碳密度(2%), 山东暖性草丛碳库总储量约为15.88 Tg C; 结缕草(Zoysia japonica)暖性草丛生态系统NEE的季节动态总体表现为夏季低, 冬季高, 非生长季节(11月至次年4月)向外界净排放CO₂, 表现为碳源效应; 生长季节(4-9月)则为净吸收CO₂ , 表现为碳汇效应, 峰值月份的平均固碳速率在-2.58- -4.46 μmol CO₂·m ^-2·s ^-1之间; 2012和2013年泰山小流域暖性草丛NEE年平均值分别为-0.43 μmol CO₂·m ^-2·s ^-1和-0.31 μmol CO₂·m ^-2·s ^-1, 都表现为碳汇效应; 光合有效辐射(PAR)、大气温度(T_a)、饱和水汽压差(VPD)和土壤10 cm深度温度(T_s)和含水量(W)是结缕草暖性草丛生态系统NEE动态的主要影响因素, 但不同月份NEE动态的影响因素各异, 且因子间存在着互作效应, 主成分分析表明, NEE的季节动态主要受温度、水分和光强等因子控制。     

Carbon stock and seasonal dynamics of carbon flux in warm-temperature tussock ecosystem in Shandong Province,China

了解山东省草地生态系统碳库现状和碳通量变化规律对于全国尺度草地生态系统碳源/汇核算有着重要的意义。该研究采用野外面上调查取样和固定加强点静态箱法(LI-840红外分析仪联用)相结合的方法, 分析了山东省暖性草丛生态系统的固碳现状、碳通量季节动态以及净生态系统CO₂交换(NEE)对各种环境因子的响应。研究结果表明: 山东暖性草丛生态系统平均碳密度为2.74 Mg C·hm ^-2, 碳密度的构成排序为土壤碳密度(89%) >生物量碳密度(9%) >凋落物碳密度(2%), 山东暖性草丛碳库总储量约为15.88 Tg C; 结缕草(Zoysia japonica)暖性草丛生态系统NEE的季节动态总体表现为夏季低, 冬季高, 非生长季节(11月至次年4月)向外界净排放CO₂, 表现为碳源效应; 生长季节(4-9月)则为净吸收CO₂ , 表现为碳汇效应, 峰值月份的平均固碳速率在-2.58- -4.46 μmol CO₂·m ^-2·s ^-1之间; 2012和2013年泰山小流域暖性草丛NEE年平均值分别为-0.43 μmol CO₂·m ^-2·s ^-1和-0.31 μmol CO₂·m ^-2·s ^-1, 都表现为碳汇效应; 光合有效辐射(PAR)、大气温度(T_a)、饱和水汽压差(VPD)和土壤10 cm深度温度(T_s)和含水量(W)是结缕草暖性草丛生态系统NEE动态的主要影响因素, 但不同月份NEE动态的影响因素各异, 且因子间存在着互作效应, 主成分分析表明, NEE的季节动态主要受温度、水分和光强等因子控制。     

Global terrestrial carbon storage and uncertainties in its temperature sensitivity examined with a simple model

The future of the land carbon sink is a significant uncertainty in global change projections. Here, key controls on global terrestrial carbon storage are examined using a simple model of vegetation and soil. Equilibrium solutions are derived as a function of atmospheric CO₂ and global temperature, these environmental variables are then linked in an idealized global change trajectory, and the lag between the dynamic and equilibrium solutions is derived for different linear rates of increase in atmospheric CO₂. Terrestrial carbon storage is departing significantly from equilibrium because CO₂ and temperature are increasing on a similar timescale to ecosystem change, and the lag is found to be proportional to the rate of forcing. Thus peak sizes of the land carbon sink, and any future land carbon source, are proportional to the rate of increase of CO₂. A switch from a land carbon sink to a source occurs at a higher CO₂ and temperature under more rapid forcing. The effects of parameter uncertainty in temperature sensitivities of photosynthesis, plant respiration and soil respiration, and structural uncertainty through the effect of fixing the ratio of plant respiration to photosynthesis are explored. In each case, the CO₂ fertilization effect on photosynthesis is constrained to reproduce the 1990 atmospheric CO₂ concentration within a closed global model. New literature compilations are presented for the temperature sensitivities of plant and soil respiration. A lower limit, Q₁₀=1.29, for soil respiration significantly increases future land carbon storage. An upper limit, Q₁₀=3.63, for soil respiration underpredicts the increase in carbon storage since the Last Glacial Maximum. Fixing the ratio of plant respiration to photosynthesis (R/P) at 0.5 generates the largest and most persistent land carbon sink, followed by the weakest land carbon source.     

Floating Aquatic Macrophytes Can Substantially Offset Open Water CO<Subscript>2</Subscript> Emissions from Tropical Floodplain Lake Ecosystems

Tropical floodplain lake ecosystems are recognized as important sources of carbon (C) from the water to the atmosphere. They receive large amounts of organic matter and nutrients from the watershed, leading to intense net heterotrophy and carbon dioxide (CO₂) emission from open waters. However, the role of extensive stands of floating macrophytes colonizing floodplains areas is still neglected in assessments of net ecosystem exchange of CO₂ (NEE). We assessed rates of air-lake CO₂ flux using static chambers in both open waters and waters covered by the widespread floating aquatic macrophyte (water hyacinth; Eichornia sp.) in two tropical floodplain lakes in Pantanal, Brazil during different hydrological seasons. In both lakes, areas colonized by floating macrophytes were a net CO₂ sink during all seasons. In contrast, open waters emitted CO₂, with higher emissions during the rising and high water periods. Our results indicate that the lake NEE can be substantially overestimated (fivefold or more in the studied lakes) if the carbon fixation by macrophytes is not considered. The contribution of these plants can lead to neutral or negative NEE (that is, net uptake of CO₂) on a yearly basis. This highlights the importance of floating aquatic macrophytes for the C balance in shallow lakes and extensive floodplain areas.     

Contribution of Sediment Respiration to Summer CO2 Emission from Low Productive Boreal and Subarctic Lakes

We measured sediment production of carbon dioxide (CO₂) and methane (CH₄) and the net flux of CO₂ across the surfaces of 15 boreal and subarctic lakes of different humic contents. Sediment respiration measurements were made in situ under ambient light conditions. The flux of CO₂ between sediment and water varied between an uptake of 53 and an efflux of 182 mg C m⁻² day⁻¹ from the sediments. The mean respiration rate for sediments in contact with the upper mixed layer (SedR) was positively correlated to dissolved organic carbon (DOC) concentration in the water (r² = 0.61). The net flux of CO₂ across the lake surface [net ecosystem exchange (NEE)] was also closely correlated to DOC concentration in the upper mixed layer (r² = 0.73). The respiration in the water column was generally 10-fold higher per unit lake area compared to sediment respiration. Lakes with DOC concentrations <5.6 mg L⁻¹ had net consumption of CO₂ in the sediments, which we ascribe to benthic primary production. Only lakes with very low DOC concentrations were net autotrophic (<2.6 mg L⁻¹) due to the dominance of dissolved allochthonous organic carbon in the water as an energy source for aquatic organisms. In addition to previous findings of allochthonous organic matter as an important driver of heterotrophic metabolism in the water column of lakes, this study suggests that sediment metabolism is also highly dependent on allochthonous carbon sources.     

Bimodality in stable isotope composition facilitates the tracing of carbon transfer from macrophytes to higher trophic levels

Even though the suitability of macrophytes to act as a carbon source to food webs has been questioned by some studies, some others indicate that macrophyte-derived carbon may play an important role in the trophic transfer of organic matter in the food web of shallow lakes. To evaluate the importance of macrophytes to food webs, we collected primary producers—macrophytes and periphyton—and consumers from 19 South American shallow lakes and analyzed their carbon stable isotopes composition (δ¹³C). Despite the diversity of inorganic carbon sources available in our study lakes, the macrophytes’ δ¹³C signatures showed a clear bimodal distribution: ¹³C-depleted and ¹³C-enriched, averaging at ?27.2 and ?13.5‰, respectively. We argue that the use of either CO₂ or HCO₃ ^? by the macrophytes largely caused the bimodal pattern in δ¹³C signals. The contribution of carbon from macrophytes to the lake’s food webs was not straightforward in most of the lakes because the macrophytes’ isotopic composition was quite similar to the isotopic composition of periphyton, phytoplankton, and terrestrial carbon. However, in some lakes where the macrophytes had a distinct isotopic signature, our data suggest that macrophytes can represent an important carbon source to shallow lake food webs.     

Potentiometric measurements of carbon dioxide flux of submerged aquatic macrophytes in pH-statted natural waters

SUMMARY. 1, An apparatus has been described that is suitable for potentiometric measurement of carbon dioxide flux in photosynthesizing shoots of submerged aquatic macrophytes 2. The procedure, based on methods described by Tailing (1973) for measurement of phytoplankton photosynthesis, relies upon the continuous pH-statting of the solution surrounding the tissues. The pH of the solution is monitored by electrodes from a pH meter which is linked to an auto-titrator. The rise in pH during photosynthesis is then compensated tor by controlled, small titrant additions of CO₂-ennched solution (titrant water). This replaces the CO₂ removed by the tissues without affecting the total alkalinity of the solution. If the concentration of CO₂ in the titrant water, and the volume of titrant added arc known precisely, the CO₂ flux can be calculated. 3. Total alkalinity, total CO₂ and free-CO₂ acidity of the bathing solutions and titrant waters are estimated by Gran titrations and the pH: tilre-volume data pairs are analysed by computer to provide rapid data feed-back. A modification to Tailing's equation for calculation of F₁functions has been necessary for accurate calibration of the CO₂enriched tilrant water. 4. The photosynthesis cuvette, which is surrounded by a water-jacket, is approximately I dm³ in capacity and has six compartments for the shoots. An impeller at the base of the cuvette rapidly mixes and cycles the bathing solution and flushes it over the tissues. 5. Information on temperature, light flux density, oxygen concentration. pH and titre-volume is continuously recorded into a data-logger and is fed into a computer which is programmed for data analyses. 6. Results from a typical experiment show the system to be sound and the method has considerable potential, especially in the study of aquatic plant photosynthesis in natural waters.     

Metabolism of dissolved organic carbon by planktonic bacteria and mixotrophic algae in lake neutralisation experiments

1. Lakes formed in mining pits often contain high concentrations of dissolved ferric iron and sulphate (e.g. 2 and 16 mmol L^?1, respectively) and the pH is buffered between 2.5 and 3.5. Efforts to neutralise their water are based on the stimulation of lake internal, bacterial iron‐ and sulphate reduction. Electron donors may be supplied by organic carbon compounds or indirectly by enhancement of primary production. Here, we investigated the function of mixotrophic algae, which can potentially supplement or deplete the organic carbon pool, in the carbon metabolism and alkalinity budget of an acidic mining lake. 2. Two weeks after organic substrates had been added in a large in situ mesocosm of 30 m diameter, a bloom of Chlamydomonas occurred, reaching a biovolume of 80 mm³ L^?1. Growth experiments using filtered lake water showed that the alga reduced the overall dissolved organic carbon (DOC) concentration despite significant photosynthetic activity. However, when Chlamydomonas were grown together with natural bacterioplankton, net DOC consumption did not increase. 3. Uptake experiments using [¹⁴C]‐glucose indicated that bacteria dominated glucose uptake and remineralisation. Therefore, the DOC leached in the water column was processed mainly by planktonic bacteria. Leached DOC must be regarded as loss, not transferred by larger organisms to the sediment, where reduction processes take place. 4. From phytoplankton biomass and production 2 years after fertilisation we estimated that pelagic photosynthesis does not supply an electron donor capacity capable of reducing more than 2% of actual stock of acidity per year. We estimated that only the benthic primary production was in a range to compensate for ongoing inputs of iron and sulphate.     

Inorganic carbon promotes photosynthesis,growth, and maximum biomass of phytoplankton in eutrophic water bodies

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Major changes in CO<Subscript>2</Subscript> efflux when shallow lakes shift from a turbid to a clear water state

Lakes can be sources or sinks of carbon, depending on local conditions. Recent studies have shown that the CO₂ efflux increases when lakes recover from eutrophication, mainly as a result of a reduction in phytoplankton biomass, leading to less uptake of CO₂ by producers. We hypothesised that lake restoration by removal of coarse fish (biomanipulation) or invasion of mussels would have a similar effect. We studied 14–22 year time series of five temperate Danish lakes and found profound effects on the calculated CO₂ efflux of major shifts in ecosystem structure. In two lakes, where limited colonisation of submerged macrophytes occurred after biomanipulation or invasion of zebra mussels (Dreissena polymorpha), the efflux increased significantly with decreasing phytoplankton chlorophyll a. In three lakes with major interannual variation in macrophyte abundance, the efflux declined with increasing macrophyte abundance in two of the lakes, while no relation to macrophytes or chlorophyll a was found in the third lake, likely due to high groundwater input to this lake. We conclude that clearing water through invasive mussels or lake restoration by biomanipulation may increase the CO₂ efflux from lakes. However, if submerged macrophytes establish and form dense beds, the CO₂ efflux may decline again.     

Interannual variation and climatic regulation of the CO2 emission from large boreal lakes

We studied the interannual variation of surface water partial pressure of CO₂ (pCO₂) and the CO₂ emissions from the 37 large Finnish lakes linking them to the water quality, catchment and climate attributes in 1996–2001. The lake water CO₂ was measured three times a year in the study lakes in 1998 and 1999 and for the rest of the years the CO₂ was modeled by measured alkalinity. The median annual CO₂ emission to the atmosphere ranged between 1.49 and 2.29 mol m^?2 a^?1. The annual CO₂ emission followed closely the annual precipitation pattern with the highest emission during the years when the precipitation was highest (r²=0.81–0.97, P<0.05). There was a strong negative correlation (r²=0.50–0.82, P<0.001) between O₂ and CO₂ saturation in the lake water during stratification suggesting effective decomposition of organic matter in the lakes. Furthermore, total phosphorus and the proportion of agricultural land in the catchment had significant positive correlations with CO₂ saturation.     

微生物介导的碳氮循环过程对全球气候变化的响应

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