潮汐作用下干湿交替对黄河三角洲盐沼湿地净生态系统CO2交换的影响

潮汐作用作为盐沼湿地独特的水文特征能在短时间内强烈影响盐沼湿地的碳平衡.利用涡度相关和微气象监测技术,对黄河三角洲盐沼湿地净生态系统CO₂交换(NEE)和环境因子进行监测,并同步监测潮汐变化,探究潮汐过程及潮汐作用下干湿交替对NEE的影响.结果表明: 潮汐过程促进了白天生态系统CO₂的吸收但未对夜晚CO₂的释放产生显著影响,潮汐淹水成为影响白天NEE的主要因子.干旱阶段和湿润阶段NEE的日平均动态均呈“U”型曲线,但干旱阶段NEE的变幅较小.干湿交替增强了白天生态系统CO₂的吸收,干旱阶段最大光合速率(A_max)、表观量子产量(α)和生态系统呼吸(R_eco)的均值均高于湿润阶段.此外,干湿交替减少了盐沼湿地夜晚NEE释放的同时增强了其温度敏感性.     

潮汐作用下干湿交替对黄河三角洲盐沼湿地净生态系统CO2交换的影响

潮汐作用作为盐沼湿地独特的水文特征能在短时间内强烈影响盐沼湿地的碳平衡.利用涡度相关和微气象监测技术,对黄河三角洲盐沼湿地净生态系统CO₂交换(NEE)和环境因子进行监测,并同步监测潮汐变化,探究潮汐过程及潮汐作用下干湿交替对NEE的影响.结果表明: 潮汐过程促进了白天生态系统CO₂的吸收但未对夜晚CO₂的释放产生显著影响,潮汐淹水成为影响白天NEE的主要因子.干旱阶段和湿润阶段NEE的日平均动态均呈“U”型曲线,但干旱阶段NEE的变幅较小.干湿交替增强了白天生态系统CO₂的吸收,干旱阶段最大光合速率(A_max)、表观量子产量(α)和生态系统呼吸(R_eco)的均值均高于湿润阶段.此外,干湿交替减少了盐沼湿地夜晚NEE释放的同时增强了其温度敏感性.     

潮汐作用对黄河三角洲盐沼湿地甲烷排放的影响

盐沼湿地作为陆海交互作用的过渡带是CH₄重要的自然来源。潮汐活动通过影响CH₄的产生、氧化和传输驱动了湿地CH₄间歇性、周期性的排放。利用涡度相关和微气象监测技术,对黄河三角洲一个盐地碱蓬生态系统CH₄通量、环境因子和水文要素（潮汐）进行了长期连续监测分析了该生态系统生长季CH₄排放的季节动态及潮汐作用对CH₄排放的影响。结果表明：生长季该生态系统是CH₄的排放源,排放日均值为0.063 mg m^-2 h^-1,（范围为-0.36-0.57 mg m^-2 h^-1）。潮汐淹水阶段和落潮后湿润阶段表现为CH₄的显著源。此外我们发现,短期潮汐活动引起土壤干湿状况的变化促进了CH₄脉冲式的排放,因此未来气候变化下温度升高和降雨季节分配引起的土壤干湿变化将会对该区域CH₄排放甚至碳循环产生积极影响。     

氮输入对滨海盐沼湿地碳循环关键过程的影响及机制

滨海盐沼湿地是缓解全球变暖的有效蓝色碳汇, 但是近岸海域富营养化导致的大量氮输入对盐沼湿地稳定性和碳汇功能构成严重威胁。潮汐作用下大量氮输入对盐沼湿地植物光合碳输入、植物-土壤碳分配和土壤碳输出等碳循环关键过程产生深刻影响, 进而影响盐沼湿地碳汇功能评估的准确性。该文从植物光合固碳、植物-土壤系统碳分配、土壤有机碳分解、土壤可溶性有机碳释放、盐沼湿地土壤碳库5个方面综述了氮输入对盐沼湿地碳循环关键过程的影响。在此基础上, 针对当前研究的不足, 提出今后的研究中, 需要进一步探究氮输入对盐沼湿地植物光合固碳及碳分配过程的影响、盐沼湿地土壤有机碳分解的微生物机制、盐沼湿地土壤可溶性有机碳产生和横向流动的影响、以及氮类型对盐沼湿地土壤碳库的影响。以期为揭示氮输入对盐沼湿地碳汇形成过程与机制提供基础资料和理论依据, 为评估未来近岸海域水体富营养化影响下滨海盐沼湿地碳库的潜在变化提供新思路。     

中国盐沼湿地蓝碳碳汇研究进展

滨海蓝碳主要指被红树林、盐沼湿地、海草床等蓝碳生态系统所固定的碳,这部分碳对于减缓气候变暖意义重大。其中盐沼湿地作为我国面积最大、分布广泛的滨海湿地,受到人类活动的扰动较多,其碳汇估算的数据缺乏系统性与完整性。通过收集我国的盐沼湿地相关研究与数据,本文对我国盐沼湿地的分布现状及其碳储量、碳埋藏、碳来源、温室气体通量进行了总结,其中我国盐沼湿地的分布面积为(1.27~3.43)×10⁵hm²,总碳储量为(7.5±0.6) Tg,碳埋藏速率为7~955 g C/(m²·a),非CO₂温室气体通量分别为23.6~986 μg CH₄/(m²·h)和1.58~110 μg N₂O/(m²·h)。本文系统梳理了有关我国盐沼湿地碳汇功能的研究,指出我国盐沼湿地碳循环研究仍需加深对机制机理的解析和关键调控因子的探究,以期让盐沼湿地蓝碳为我国的碳达峰与碳中和战略做出更大贡献。     

干湿交替和冻融作用对土壤肥力和生态环境的影响

干湿交替和冻融作用对土壤肥力和生态环境的影响朴河春,刘广深,洪业汤（中国科学院地球化学研究所,贵阳５５０００２）ＥｆｆｅｃｔｓｏｆＡｌｔｅｒｎａｔｉｖｅＤｒｙｉｎｇ－ＲｅｗｅｔｔｉｎｇａｎｄＦｒｅｅｚｉｎｇ－ＴｈａｗｉｎｇｏｎｓｏｉｌＦｅｒｔｉｌｉｔ...     

中国滨海盐沼湿地碳收支与碳循环过程研究进展

滨海盐沼湿地由于其较高的初级生产力和较缓慢的有机质降解速率而成为缓解全球变暖的有效蓝色碳汇,近年来引起全球范围内的热切关注.我国滨海盐沼湿地分布较广,国内学者对滨海盐沼湿地碳循环及碳收支研究取得了一定进展,深入研究滨海盐沼湿地碳循环有助于对全球碳循环及全球变化的理解,并为利用滨海湿地进行碳的增汇减排提供科学依据.主要从我国滨海盐沼湿地碳循环主要观测方法、碳收支与碳循环过程及特点、碳库的组成与影响因素、气态碳的输入输出、潮汐作用对其碳收支的影响这5个方面出发,对国内的滨海盐沼湿地碳循环与碳收支的研究进展进行了归纳总结,并对今后的研究方向给出如下建议:(1)加强滨海盐沼湿地土壤碳库在深度上和广度上的研究;(2)标准化滨海盐沼湿地碳储量、碳通量的量化方法和观测技术;(3)在研究尺度上要宏观、微观并重,同时加强长期原位监测湿地碳通量的变化与室内模拟研究;(4)量化在潮汐影响下滨海盐沼湿地碳与邻近生态系统之间的横向交换通量.只有对我国滨海盐沼湿地碳库收支进行更准确的评估和长期的碳库动态变化监测,方可进一步认识我国盐沼湿地对全球气候变化的影响及其反馈作用,这对于预测全球变化及制定湿地碳储备功能的提升策略具有重要的意义.     

滨海盐沼湿地有机碳的沉积与埋藏研究进展

滨海盐沼湿地有着较高的碳沉积速率和固碳能力,在缓解全球变暖方面发挥着重要作用,而盐渍土壤是滨海盐沼湿地碳收支研究中最大的有机碳库,研究其碳沉积与埋藏对于理解滨海湿地碳收支有着重要的意义.本文从滨海盐沼湿地土壤有机碳的来源、土壤有机碳库与沉积速率、盐沼湿地有机碳的埋藏机制、全球变化与滨海盐沼湿地碳封存等几方面对滨海盐沼湿地有机碳沉积与埋藏的相关研究进行综述.今后研究应侧重:1)加强对控制滨海盐沼湿地碳储存变异的基本因素的迸一步研究;2)对测量滨海盐沼湿地沉积物碳储量和沉积碳埋藏速率的方法进行标准化;3)对潮汐影响下滨海盐沼湿地碳与邻近生态系统之间的横向交换通量进行量化;4)探明全球变暖的影响和生产力的提高是否可以抵消因呼吸增强而造成的有机碳降解速率的升高.确定固碳速率变化驱动因子,理解气候变化和人类活动对碳埋藏的影响机制,有助于提升我国滨海盐沼湿地的固碳能力.     

降雨量和降雨时间共同调控黄河三角洲典型盐沼湿地土壤碳矿化

研究降雨格局(如降雨量和降雨时间)对滨海盐沼湿地土壤碳矿化的影响,对于深入理解土壤碳的稳定性和积累机制具有重要意义.本研究选取远离海岸且不受潮汐影响的黄河三角洲原生盐地碱蓬盐沼湿地为对象,通过野外原状土柱的控制试验,分析土壤碳矿化(CO2和CH4通量)在不同时期(干旱期和湿润期)对降雨事件的响应.结果表明:降雨时间和降...     

滨海盐沼湿地有机碳的沉积与埋藏研究进展

滨海盐沼湿地有着较高的碳沉积速率和固碳能力,在缓解全球变暖方面发挥着重要作用,而盐渍土壤是滨海盐沼湿地碳收支研究中最大的有机碳库,研究其碳沉积与埋藏对于理解滨海湿地碳收支有着重要的意义.本文从滨海盐沼湿地土壤有机碳的来源、土壤有机碳库与沉积速率、盐沼湿地有机碳的埋藏机制、全球变化与滨海盐沼湿地碳封存等几方面对滨海盐沼湿地有机碳沉积与埋藏的相关研究进行综述.今后研究应侧重:1)加强对控制滨海盐沼湿地碳储存变异的基本因素的进一步研究;2)对测量滨海盐沼湿地沉积物碳储量和沉积碳埋藏速率的方法进行标准化;3)对潮汐影响下滨海盐沼湿地碳与邻近生态系统之间的横向交换通量进行量化;4)探明全球变暖的影响和生产力的提高是否可以抵消因呼吸增强而造成的有机碳降解速率的升高.确定固碳速率变化驱动因子,理解气候变化和人类活动对碳埋藏的影响机制,有助于提升我国滨海盐沼湿地的固碳能力.     

基于CASA模型的长江口崇明东滩湿地植被净初级生产力与固碳潜力

湿地生态系统具有很强的储碳、固碳能力,在全球碳循环中占有重要地位.为了解盐沼的固碳能力,以崇明东滩南部典型盐沼潮沟体系为对象,结合实验观测与遥感影像解译,估算了盐沼湿地的净初级生产力,并探讨了环境变化下盐沼湿地固碳潜力的变化.结果 表明:盐沼植物净初级生产力表现出显著的时空差异,时间差异体现在年际和季节差异,即2013...     

The flume design — a methodology for evaluating material fluxes between a vegetated salt marsh and the adjacent tidal creek

An experimental flume is described which can be used as a tool to assess whether a vegetated marsh surface is a source or sink for nutrients via tidal inundation. An initial calibration study (two tidal cycles) was conducted to determine the optimum sampling design and aid in model development for flux calculations. A statistical analysis of the data showed a negligible concentration difference as a function of water depth for most of the constituents analyzed. This coupled with the low tidal velocities over the marsh surface (<1.5cm/s) suggested that a volumetric model was adequate for calculations of instantaneous discharge and nutrient flux through any station perpendicular to tidal flow. The resultant instantaneous mass flux calculations showed that water discharge was one of the dominant factors controlling the movement of material. A sine-cosine statistical model utilizing the main tidal periodicities was designed to: (1) model the instantaneous fluxes, (2) calculate the average net flux of suspended and dissolved materials, and (3) test the hypothesis that the average net flux equals zero versus a two-sided alternative using a standard regression t-test.     

Microbial carbon monoxide consumption in salt marsh sediments

We have examined sediments from a fringing salt marsh in Maine to further understand marine CO metabolism, about which relatively little is known. Intact cores from the marsh emitted CO during dark oxic incubations, but emission rates were significantly higher during anoxic incubations, which provided evidence for simultaneous production and aerobic consumption in surface sediments. CO emission rates were also elevated when cores were exposed to light, which indicated that photochemical reactions play a role in CO production. A kinetic analysis of marsh surface sediments yielded an apparent K(m) of about 82 ppm, which exceeded values reported for well-aerated soils that consume atmospheric CO (65nM). Surface (0-0.2 cm depth interval) sediment slurries incubated under oxic conditions rapidly consumed CO, and methyl fluoride did not inhibit uptake, which indicated that neither ammonia nor methane oxidizers contributed to the observed activity. In contrast, aerobic CO uptake was inhibited by additions of readily available organic substrates (pyruvate, glucose and glycine), but not by cellulose. CO was also consumed by surface and sub-surface sediment slurries incubated under anaerobic conditions, but rates were less than during aerobic incubations. Molybdate and nitrate or nitrite, but not 2-bromoethanesulfonic acid, partially inhibited anaerobic uptake. These results suggest that sulfidogens and acetogens, but not dissimilatory nitrate reducers or methanogens, actively consume CO. Sediment-free plant roots also oxidized CO aerobically; rates for Spartina patens and Limonium carolinianum roots were significantly higher than rates for Spartina alterniflora roots. Thus plants may also impact CO cycling in estuarine environments.     

Long‐term organic carbon sequestration in tidal marsh sediments is dominated by old‐aged allochthonous inputs in a macrotidal estuary

Tidal marshes are vegetated coastal ecosystems that are often considered as hotspots of atmospheric CO₂ sequestration. Although large amounts of organic carbon (OC) are indeed being deposited on tidal marshes, there is no direct link between high OC deposition rates and high OC sequestration rates due to two main reasons. First, the deposited OC may become rapidly decomposed once it is buried and, second, a significant part of preserved OC may be allochthonous OC that has been sequestered elsewhere. In this study we aimed to identify the mechanisms controlling long‐term OC sequestration in tidal marsh sediments along an estuarine salinity gradient (Scheldt estuary, Belgium and the Netherlands). Analyses of deposited sediments have shown that OC deposited during tidal inundations is up to millennia old. This allochthonous OC is the main component of OC that is effectively preserved in these sediments, as indicated by the low radiocarbon content of buried OC. Furthermore, OC fractionation showed that autochthonous OC is decomposed on a decadal timescale in saltmarsh sediments, while in freshwater marsh sediments locally produced biomass is more efficiently preserved after burial. Our results show that long‐term OC sequestration is decoupled from local biomass production in the studied tidal marsh sediments. This implies that OC sequestration rates are greatly overestimated when they are calculated based on short‐term OC deposition rates, which are controlled by labile autochthonous OC inputs. Moreover, as allochthonous OC is not sequestered in‐situ, it does not contribute to active atmospheric CO₂ sequestration in these ecosystems. A correct assessment of the contribution of allochthonous OC to the total sedimentary OC stock in tidal marsh sediments as well as a correct understanding of the long‐term fate of locally produced OC are both necessary to avoid overestimations of the rate of in‐situ atmospheric CO₂ sequestration in tidal marsh sediments.