Flux of reduced chemical constituents (Fe2+, Mn2+, NH inf4 sup+ and CH4) and sediment oxygen demand in Lake Erie

Sediment pore water concentrations of Fe²⁺, Mn²⁺, NH _inf4 ^sup+ and CH₄ were analyzed from both diver-collected cores and anin situ equilibration device (peeper) in Lake Erie's central basin. Sediment oxygen demand (SOD) was measured at the same station with a hemispheric chamber (including DO probe and recorder) subtending a known area of sediments. The average SOD was 9.4 mM m⁻² day⁻¹ (0.3 g m⁻² day⁻¹). From pore water gradients within the near-surface zone, the chemical flux across the interface was calculated indirectly using Fick's first law modified for sediments. These calculations, using core and peeper gradients, always showed sediment loss to overlying waters, and variations between the two techniques differed by less than an order of magnitude for Fe²⁺ and CH₄. The transport of these reduced constituents can represent a sizeable oxygen demand, ranging from less than 1% for Fe²⁺ and Mn²⁺ to as high as 26% for NH _inf4 ^sup+ , and 30% for CH₄. The average flux of these constituents could account for about a third of the SOD at the sediment-water interface of this station.     

Phosphorus alleviation of nitrogen‐suppressed methane sink in global grasslands

Grassland ecosystems account for more than 10% of the global CH₄ sink in soils. A 4‐year field experiment found that addition of P alone did not affect CH₄ uptake and experimental addition of N alone significantly suppressed CH₄ uptake, whereas concurrent N and P additions suppressed CH₄ uptake to a lesser degree. A meta‐analysis including 382 data points in global grasslands corroborated these findings. Global extrapolation with an empirical modelling approach estimated that contemporary N addition suppresses CH₄ sink in global grassland by 11.4% and concurrent N and P deposition alleviates this suppression to 5.8%. The P alleviation of N‐suppressed CH₄ sink is primarily attributed to substrate competition, defined as the competition between ammonium and CH₄ for the methane mono‐oxygenase enzyme. The N and P impacts on CH₄ uptake indicate that projected increases in N and P depositions might substantially affect CH₄ uptake and alter the global CH₄ cycle.     

Influence of temperature on the δ13C values and distribution of methanotroph‐related hopanoids in Sphagnum‐dominated peat bogs

Methane emissions from peat bogs are mitigated by methanotrophs, which live in symbiosis with peat moss (e.g. Sphagnum). Here, we investigate the influence of temperature and resultant changes in methane fluxes on Sphagnum and methanotroph‐related biomarkers, evaluating their potential as proxies in ancient bogs. A pulse‐chase experiment using ¹³C‐labelled methane in the field clearly showed label uptake in diploptene, a biomarker for methanotrophs, demonstrating in situ methanotrophic activity in Sphagnum under natural conditions. Peat cores containing live Sphagnum were incubated at 5, 10, 15, 20 and 25°C for two months, causing differences in net methane fluxes. The natural δ¹³C values of diploptene extracted from Sphagnum showed a strong correlation with temperature and methane production. The δ¹³C values ranged from ?34‰ at 5°C to ?41‰ at 25°C. These results are best explained by enhanced expression of the methanotrophic enzymatic isotope effect at higher methane concentrations. Hence, δ¹³C values of diploptene, or its diagenetic products, potentially provide a useful tool to assess methanotrophic activity in past environments. Increased methane fluxes towards Sphagnum did not affect δ¹³C values of bulk Sphagnum and its specific marker, the C₂₃ n‐alkane. The concentration of methanotroph‐specific bacteriohopanepolyols (BHPs), aminobacteriohopanetetrol (aminotetrol, characteristic for type II and to a lesser extent type I methanotrophs) and aminobacteriohopanepentol (aminopentol, a marker for type I methanotrophs) showed a non‐linear response to increased methane fluxes, with relatively high abundances at 25°C compared to those at 20°C or below. Aminotetrol was more abundant than aminopentol, in contrast to similar abundances of aminotetrol and aminopentol in fresh Sphagnum. This probably indicates that type II methanotrophs became prevalent under the experimental conditions relative to type I methanotrophs. Even though BHP concentrations may not directly reflect bacterial activity, they may provide insight into the presence of different types of methanotrophs.     

Where old meets new: An ecosystem study of methanogenesis in a reflooded agricultural peatland

Reflooding formerly drained peatlands has been proposed as a means to reduce losses of organic matter and sequester soil carbon for climate change mitigation, but a renewal of high methane emissions has been reported for these ecosystems, offsetting mitigation potential. Our ability to interpret observed methane fluxes in reflooded peatlands and make predictions about future flux trends is limited due to a lack of detailed studies of methanogenic processes. In this study we investigate methanogenesis in a reflooded agricultural peatland in the Sacramento Delta, California. We use the stable‐and radio‐carbon isotopic signatures of wetland sediment methane, ecosystem‐scale eddy covariance flux observations, and laboratory incubation experiments, to identify which carbon sources and methanogenic production pathways fuel methanogenesis and how these processes are affected by vegetation and seasonality. We found that the old peat contribution to annual methane emissions was large (~30%) compared to intact wetlands, indicating a biogeochemical legacy of drainage. However, fresh carbon and the acetoclastic pathway still accounted for the majority of methanogenesis throughout the year. Although temperature sensitivities for bulk peat methanogenesis were similar between open‐water (Q₁₀ = 2.1) and vegetated (Q₁₀ = 2.3) soils, methane production from both fresh and old carbon sources showed pronounced seasonality in vegetated zones. We conclude that high methane emissions in restored wetlands constitute a biogeochemical trade‐off with contemporary carbon uptake, given that methane efflux is fueled primarily by fresh carbon inputs.     

Methane emissions reduce the radiative cooling effect of a subtropical estuarine mangrove wetland by half

The role of coastal mangrove wetlands in sequestering atmospheric carbon dioxide (CO₂) and mitigating climate change has received increasing attention in recent years. While recent studies have shown that methane (CH₄) emissions can potentially offset the carbon burial rates in low‐salinity coastal wetlands, there is hitherto a paucity of direct and year‐round measurements of ecosystem‐scale CH₄ flux (F_CH4) from mangrove ecosystems. In this study, we examined the temporal variations and biophysical drivers of ecosystem‐scale F_CH4 in a subtropical estuarine mangrove wetland based on 3 years of eddy covariance measurements. Our results showed that daily mangrove F_CH4 reached a peak of over 0.1 g CH₄‐C m^?2 day^?1 during the summertime owing to a combination of high temperature and low salinity, while the wintertime F_CH4 was negligible. In this mangrove, the mean annual CH₄ emission was 11.7 ± 0.4 g CH₄‐C m^–2 year^?1 while the annual net ecosystem CO₂ exchange ranged between ?891 and ?690 g CO₂‐C m^?2 year^?1, indicating a net cooling effect on climate over decadal to centurial timescales. Meanwhile, we showed that mangrove F_CH4 could offset the negative radiative forcing caused by CO₂ uptake by 52% and 24% over a time horizon of 20 and 100 years, respectively, based on the corresponding sustained‐flux global warming potentials. Moreover, we found that 87% and 69% of the total variance of daily F_CH4 could be explained by the random forest machine learning algorithm and traditional linear regression model, respectively, with soil temperature and salinity being the most dominant controls. This study was the first of its kind to characterize ecosystem‐scale F_CH4 in a mangrove wetland with long‐term eddy covariance measurements. Our findings implied that future environmental changes such as climate warming and increasing river discharge might increase CH₄ emissions and hence reduce the net radiative cooling effect of estuarine mangrove forests.     

施硅对增温稻田CH4和N2O排放的影响

夜间增温幅度大于白天是气候变暖的显著特征。夜间增温影响水稻生产及CH4和N2O排放。硅是作物有益元素,施硅可提高产量,减少稻田CH4排放。增温或施硅单因子对稻田CH4和N2O排放影响已有报道,但二者耦合如何影响水稻生产及稻田CH4和N2O排放,尚不清楚。通过田间模拟试验,研究了夜间增温下施硅对水稻生长、产量及温室气体持续增温/冷却潜势和排放强度的影响。采用铝箔反光膜夜间(19:00-6:00)覆盖水稻冠层进行模拟夜间增温试验。增温设2水平,即常温对照(CK)和夜间增温(NW);施硅量设2水平,即Si0(不施硅)和Si1(钢渣硅肥,200 kgSiO2/ha)。结果表明,施硅可缓解夜间增温对水稻根系活力的抑制作用,降低夜间增温对水稻地上部、地下部干重和产量的抑制作用。夜间增温显著提高CH4累计排放量,而施硅显著降低CH4累计排放量。夜间增温下施硅处理稻田CH4累计排放量在分蘖期、拔节期、抽穗-扬花期和灌浆成熟期比未施硅处理分别低48.12%、49.16%、61.59%和39.13%。夜间增温或施硅均促进稻田N2O排放,夜间增温下施硅在上述生育期以及全生育期的累计排放量依次比对照高78.17%、51.45%、52.01%、26.14%和40.70%。研究认为,施硅可缓解夜间增温对稻田综合增温潜势和排放强度的促进作用。     

典型温带雨养泥炭沼泽湿地地下部二氧化碳和甲烷浓度变化规律及其影响因素

为研究北方泥炭沼泽湿地二氧化碳（CO₂）和甲烷（CH₄）浓度随深度的变化规律及其影响因素,选取欧洲北部典型雨养泥炭地贝尔山湿地（BBM）和舒特兹山湿地（SBM）两个采样点,通过原位采集泥炭剖面温室气体、孔隙水以及土壤样品,结合傅里叶变换红外光谱（FTIR）技术、碳氮同位素技术,探讨泥炭土壤的分解程度及温室气体浓度变化的关系。研究结果表明：（1）BBM采样点地下部的CO₂浓度变化规律总体呈现随深度波动减少趋势,值多在3000 μmol/L附近波动,最大值为4210.74 μmol/L（120 cm）,SBM采样点的CO₂浓度随深度先增后减,60 cm以上在1800 μmol/L附近波动,60 cm以下在3000 μmol/L附近波动,最大值为4191.94 μmol/L（90 cm）;BBM和SBM地下部CH₄浓度都随深度增大,并且在60cm以下浓度增加较快,BBM最大值为735.90 μmol/L（260 cm）,SBM最大值为543.51 μmol/L（170 cm）。（2）BBM和SBM的δ¹³C_CH4的值均较小,表明大部分的¹²CH₄仍被储存在泥炭土壤中,而两个采样点的δ¹³C_CO2和分馏系数α_c均随深度增加,表明泥炭土中产甲烷方式为浅层以乙酸产甲烷为主,深层以H₂还原CO₂为主。（3）C/N、碳氮同位素比值、FTIR均显示SBM和BBM的有机质分解程度较低,因为两个采样点的低可溶性有机碳浓度和低pH值不利于分解,表明该地储存着大量有机碳。通过探讨北温带典型泥炭地温室气体的浓度变化规律及其影响因素,结果可为全球泥炭湿地碳排放提供理论支撑。     

水位下降对若尔盖泥炭地垂直剖面土壤甲烷产生及厌氧氧化潜势的影响

泥炭地是主要的甲烷（CH₄）排放源,甲烷循环过程对水位变化响应敏感。研究选取两块具有水位差异的泥炭地土壤,通过厌氧培养实验探究水位变化对泥炭地甲烷产生和甲烷厌氧氧化（Methane Anaerobic Oxidation,AOM）潜势的影响,并分析影响其潜势大小的生物地球化学因子。结果显示,高水位泥炭地（0 cm） CH₄产生累积量为（0.89±0.01）μg/g,要显著高于低水位（-30 cm：（0.70±0.03）μg/g）泥炭地甲烷产生量,但低水位AOM累积量要显著高于高水位泥炭地（0 cm：（2829.93±35.99）μg/g）,低水位泥炭地AOM量为（3588.06±24.78）μg/g。通过相关性分析发现甲烷产生潜势与含水量和DOC具有显著相关性,AOM潜势与含水量、pH、DOC具有显著相关性,含水量和DOC是影响若尔盖泥炭地甲烷产生及AOM潜势大小的重要因子。此外,发现高水位泥炭地甲烷产生潜势对温度升高的响应较为明显,特别是表层土壤（0-20 cm）。本研究明确了水位变化对若尔盖泥炭地甲烷产生及AOM潜势的影响特征,估算了全国泥炭地甲烷产生及AOM潜势的大小,以期为减缓全球气候变暖提供一定的理论支撑。     

甲烷生物利用及嗜甲烷菌的工程改造

作为来源广泛、储量丰富的有机碳一气体,甲烷被认为是下一代工业生物技术中最具潜力的碳原料之一。嗜甲烷菌能够利用其体内的甲烷单加氧化酶,将甲烷作为唯一的碳源和能源进行生长和代谢,这为温室气体减排及其开发利用提供了新的策略。目前,嗜甲烷菌生物催化体系的相关研究已开展多年,随着系统生物学和合成生物学的快速发展,利用代谢工程合理改造嗜甲烷菌代谢途径以提高甲烷转化效率,已经实现了生物转化甲烷制备多种大宗化学品和生物燃料。本文详细讨论并介绍了嗜甲烷菌催化氧化甲烷的相关代谢途径、高效细胞工厂构建及部分化学品生物合成的最新研究进展,并对甲烷生物转化未来的发展方向和面临的技术挑战进行了讨论和展望。