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Organic Coatings Reduce Dissolution Rate by an Order of Magnitude for Carbonate Minerals Produced by Marine Fish 有机涂层将海洋鱼类产生的碳酸盐矿物的溶解率降低了一个数量级
IF 5.4 2区 地球科学 Q1 ENVIRONMENTAL SCIENCES Pub Date : 2024-11-13 DOI: 10.1029/2024GB008176
Amanda M. Oehlert, Sarah Walls, Katelyn Arista, Jazmin Garza, Erik J. Folkerts, Brooke E. Vitek, Sadegh Tale Masoule, Clément G. L. Pollier, Gaëlle Duchâtellier, John D. Stieglitz, Daniel D. Benetti, Rachael M. Heuer, Ali Ghahremaninezhad, Martin Grosell

Marine carbonate production and dissolution are important components of the global carbon cycle and the marine alkalinity budget. Global carbonate production by marine fish (ichthyocarbonate) has been estimated to be as high as 9.03 Pg CaCO3 yr−1; however, the fate of ichthyocarbonate is poorly understood. High magnesium concentrations in ichthyocarbonate would traditionally suggest rapid dissolution under current marine conditions, but a correlation between dissolution rate and mol%MgCO3 has not been observed. Here, we aim to determine the role of organic coatings on dissolution rates of ichthyocarbonate in marine environments. We applied a combination of petrographic, geochemical, and microCT approaches to assess the quantity and distribution of organic matter in ichthyocarbonate produced by two species of marine fish, the Gulf toadfish (Opsanus beta) and the Olive flounder (Paralichthys olivaceus). We show that organic matter, including external coatings and embedded organic material, is volumetrically significant, ranging from 8.5% to 32.3% of ichthyocarbonate by volume. Bleach oxidation of external organic matter coatings increased the dissolution rate of ichthyocarbonate by more than an order of magnitude, suggesting these coatings serve to reduce reactive surface area of the mineral fraction in ichthyocarbonate. Assuming that organic coatings do not influence sinking rates, external coatings extend the depth of ichthyocarbonate persistence in the water column by ∼12–15×. Therefore, organic coatings are an important determinant of the role of ichthyocarbonate in the marine carbon cycle.

海洋碳酸盐的产生和溶解是全球碳循环和海洋碱度预算的重要组成部分。据估计,海洋鱼类(鱼碳酸盐)的全球碳酸盐产量高达每年 9.03 Pg CaCO3;然而,人们对鱼碳酸盐的归宿却知之甚少。鱼碳酸盐中的高镁浓度传统上表明,在当前海洋条件下,鱼碳酸盐的溶解速度很快,但尚未观察到溶解速度与 mol%MgCO3 之间的相关性。在此,我们旨在确定有机涂层对海洋环境中鱼鳞碳酸盐溶解速率的作用。我们结合岩石学、地球化学和显微 CT 方法,评估了两种海洋鱼类--海湾蟾蜍鱼(Opsanus beta)和橄榄鲽(Paralichthys olivaceus)--产生的鱼碳酸盐中有机物的数量和分布。我们的研究表明,有机物(包括外部涂层和嵌入的有机物)在体积上非常重要,占鱼类碳酸酯体积的 8.5% 到 32.3%。外部有机物涂层的漂白氧化作用使鱼类碳酸盐的溶解速率增加了一个数量级以上,这表明这些涂层起到了减少鱼类碳酸盐中矿物部分反应表面积的作用。假设有机涂层不影响下沉速度,则外部涂层可将鱼碳酸盐在水体中的存留深度延长 12-15 倍。因此,有机涂层是鱼碳酸盐在海洋碳循环中发挥作用的重要决定因素。
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引用次数: 0
210Po and 210Pb Distributions Along the GEOTRACES Pacific Meridional Transect (GP15): Tracers of Scavenging and Particulate Organic Carbon (POC) Export 沿 GEOTRACES 太平洋经向横断面(GP15)的 210Po 和 210Pb 分布:清扫和颗粒有机碳(POC)输出的示踪剂
IF 5.4 2区 地球科学 Q1 ENVIRONMENTAL SCIENCES Pub Date : 2024-11-03 DOI: 10.1029/2024GB008243
J. Kirk Cochran, Ziran Wei, Evan Horowitz, Patrick Fitzgerald, Christina Heilbrun, Mark Stephens, Phoebe J. Lam, Emilie Le Roy, Matthew Charette

Distributions of the natural radionuclide 210Po and its grandparent 210Pb along the GP15 Pacific Meridional Transect provide information on scavenging rates of reactive chemical species throughout the water column and fluxes of particulate organic carbon (POC) from the primary production zone (PPZ). 210Pb is in excess of its grandparent 226Ra in the upper 400–700 m due to the atmospheric flux of 210Pb. Mid-water 210Pb/226Ra activity ratios are close to radioactive equilibrium (1.0) north of ∼20°N, indicating slow scavenging, but deficiencies at stations near and south of the equator suggest more rapid scavenging associated with a “particle veil” located at the equator and hydrothermal processes at the East Pacific Rise. Scavenging of 210Pb and 210Po is evident in the bottom 500–1,000 m at most stations due to enhanced removal in the nepheloid layer. Deficits in the PPZ of 210Po (relative to 210Pb) and 210Pb (relative to 226Ra decay and the 210Pb atmospheric flux), together with POC concentrations and particulate 210Po and 210Pb activities, are used to calculate export fluxes of POC from the PPZ. 210Po-derived POC fluxes on large (>51 μm) particles range from 15.5 ± 1.3 mmol C/m2/d to 1.5 ± 0.2 mmol C/m2/d and are highest in the Subarctic North Pacific; 210Pb-derived fluxes range from 6.7 ± 1.8 mmol C/m2/d to 0.2 ± 0.1 mmol C/m2/d. Both 210Po- and 210Pb-derived POC fluxes are greater than those calculated using the 234Th proxy, possibly due to different integration times of the radionuclides, considering their different radioactive mean-lives and scavenging mean residence times.

沿 GP15 太平洋经向横断面天然放射性核素 210Po 及其祖代 210Pb 的分布,提供了有关整个水体中活性化学物种清除率以及初级生产区(PPZ)颗粒有机碳通量的信息。由于大气中 210Pb 的通量,在上 400-700 米处,210Pb 超过了其祖先 226Ra。北纬 20°以北的中层水 210Pb/226Ra 放射性活度比接近放射性平衡(1.0),表明清除速度较慢,但赤道附近和以南的观测站点的放射性活度比不足,表明清除速度较快,这与赤道的 "粒子幔 "和东太平洋海隆的热液过程有关。在大多数站点,由于肾胶体层的清除作用增强,210Pb 和 210Po 的清除作用在底部 500-1,000 米处十分明显。PPZ 中 210Po(相对于 210Pb)和 210Pb(相对于 226Ra 衰减和 210Pb 大气通量)的缺失,以及 POC 浓度和微粒 210Po 和 210Pb 活性,用于计算 PPZ 的 POC 出口通量。大颗粒(51 μm)上 210Po 导出的 POC 通量从 15.5 ± 1.3 mmol C/m2/d 到 1.5 ± 0.2 mmol C/m2/d,在北太平洋亚北极地区最高;210Pb 导出的通量从 6.7 ± 1.8 mmol C/m2/d 到 0.2 ± 0.1 mmol C/m2/d。210Po和210Pb衍生的POC通量都大于使用234Th替代值计算的通量,这可能是由于放射性核素的积分时间不同,考虑到它们不同的放射性平均寿命和清除平均停留时间。
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引用次数: 0
Extreme Climate as the Primary Control of Global Soil Organic Carbon Across Spatial Scales 极端气候是跨空间尺度全球土壤有机碳的主要控制因素
IF 5.4 2区 地球科学 Q1 ENVIRONMENTAL SCIENCES Pub Date : 2024-11-01 DOI: 10.1029/2024GB008200
Yucheng Wei, Mingming Wang, R. A. Viscarra Rossel, Hong Chen, Zhongkui Luo

Soil organic carbon (SOC) stock exhibits substantial variability across spatial scales and depths. Drivers of such variability may be scale- and depth-dependent, but have been rarely systematically investigated. Assessing SOC measurements of 113,013 soil profiles worldwide, we show that climate, encompassing mean modern- and paleo-climate and climate extremes, is the predominant determinant across scales (from 50 km to the globe) and depths, explaining 34%–62% of the spatial variability of SOC stocks depending on the spatial scale and soil depth layer assessed. On finer scales (50–100 km), soil properties and mean modern- and paleo-climate are dominant in all soil depth layers. At broader scales (>100 km), the significance of climate extremes intensifies, alone explaining 27%–32% of the spatial variability of SOC stocks. Furthermore, we find nonlinear relationships of SOC stocks with most factors, while the relationship with the same factor is distinct across scales and depths. These results reinforce climate, particularly extremes, as the primary driving force of whole-soil carbon distribution across the globe, emphasizing the need to factor extremes into carbon management strategies.

土壤有机碳(SOC)储量在不同的空间尺度和深度有很大的变化。这种变化的驱动因素可能与尺度和深度有关,但却很少得到系统的研究。通过对全球 113,013 个土壤剖面的 SOC 测量结果进行评估,我们发现气候(包括现代和古气候平均值以及极端气候)是跨尺度(从 50 千米到全球)和深度的主要决定因素,根据所评估的空间尺度和土壤深度层,可解释 34%-62% 的 SOC 储量空间变异性。在更细的尺度上(50-100 千米),土壤特性以及现代和古气候的平均值在所有土壤深度层中都占主导地位。在更宽的尺度上(100 千米),极端气候的重要性进一步加强,仅此一项就能解释 27%-32% 的 SOC 储量空间变异性。此外,我们还发现 SOC 储量与大多数因子之间存在非线性关系,而同一因子与不同尺度和深度之间的关系也各不相同。这些结果强化了气候,尤其是极端气候,是全球全土碳分布的主要驱动力,强调了将极端气候因素纳入碳管理战略的必要性。
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引用次数: 0
A Comprehensive Analysis of Air-Sea CO2 Flux Uncertainties Constructed From Surface Ocean Data Products 根据表层海洋数据产品构建的海气二氧化碳通量不确定性综合分析
IF 5.4 2区 地球科学 Q1 ENVIRONMENTAL SCIENCES Pub Date : 2024-11-01 DOI: 10.1029/2024GB008188
Daniel J. Ford, Josh Blannin, Jennifer Watts, Andrew J. Watson, Peter Landschützer, Annika Jersild, Jamie D. Shutler

Increasing anthropogenic CO2 emissions to the atmosphere are partially sequestered into the global oceans through the air-sea exchange of CO2 and its subsequent movement to depth, commonly referred to as the global ocean carbon sink. Quantifying this ocean carbon sink provides a key component for closing the global carbon budget, which is used to inform and guide policy decisions. These estimates are typically accompanied by an uncertainty budget built by selecting what are perceived as critical uncertainty components based on selective experimentation. However, there is a growing realization that these budgets are incomplete and may be underestimated, which limits their power as a constraint within global budgets. In this study, we present a methodology for quantifying spatially and temporally varying uncertainties in the air-sea CO2 flux calculations for the fCO2-product based assessments that allows an exhaustive assessment of all known sources of uncertainties, including decorrelation length scales between gridded measurements, and the approach follows standard uncertainty propagation methodologies. The resulting standard uncertainties are higher than previously suggested budgets, but the component contributions are largely consistent with previous work. The uncertainties presented in this study identify how the significance and importance of key components change in space and time. For an exemplar method (the UExP-FNN-U method), the work identifies that we can currently estimate the annual ocean carbon sink to a precision of ±0.70 Pg C yr−1 (1σ uncertainty). Because this method has been built on established uncertainty propagation and approaches, it appears that applicable to all fCO2-product assessments of the ocean carbon sink.

大气中不断增加的人为二氧化碳排放量通过二氧化碳的海气交换及其随后向深海的移动被部分封存到全球海洋中,这就是通常所说的全球海洋碳汇。对海洋碳汇进行量化是关闭全球碳预算的一个关键组成部分,用于为政策决策提供信息和指导。这些估算通常伴随着不确定性预算,不确定性预算是在选择性实验的基础上选择被认为是关键的不确定性成分而建立的。然而,越来越多的人意识到这些预算是不完整的,可能被低估了,这限制了它们在全球预算中的约束作用。在本研究中,我们提出了一种方法,用于量化基于 fCO2 产品评估的空气-海洋 CO2 通量计算中空间和时间变化的不确定性,该方法允许对所有已知的不确定性来源进行详尽评估,包括网格测量之间的相关长度尺度,并且该方法遵循标准的不确定性传播方法。由此得出的标准不确定性高于之前建议的预算,但各组成部分的贡献与之前的工作基本一致。本研究提出的不确定性确定了关键要素的重要性在空间和时间上的变化。对于一种示例方法(UExP-FNN-U 方法),研究发现我们目前可以估算出每年海洋碳汇的精度为 ±0.70 Pg C yr-1(不确定性为 1σ)。由于该方法建立在既定的不确定性传播和方法之上,因此似乎适用于对海洋碳汇的所有 fCO2 产物评估。
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引用次数: 0
Setting Up Methane Mitigation Measures for Indian Rice Fields: Representative Emissions and New Interpretations 为印度稻田制定甲烷减排措施:代表性排放和新解释
IF 5.4 2区 地球科学 Q1 ENVIRONMENTAL SCIENCES Pub Date : 2024-10-29 DOI: 10.1029/2024GB008107
Fida Mohammad Sahil, Mukund Narayanan, Idhayachandhiran Ilampooranan

Rice cultivation produces methane (CH4) due to anaerobic conditions induced by flood irrigation, significantly contributing to global warming. While most studies use national emission factors (EFs), our study synthesized 726 published measurements across India (the second largest methane emitter after China) to develop district-level water regime-specific EFs for estimating district-scale emissions and warming potential. CH4 emissions from Indian rice fields increased from 3.7 (3.4–4.1) Tg to 4.8 (4.4–5.3) Tg during 1966–2017, driven by rice area and water-regime variations. Meanwhile, district-level emissions increased by ∼930%, influenced by management practices such as animal manure, fertilizer application, and water input, accurately reflecting regional variations compared to previous estimates. Employing a novel muti-output random forest mitigation model (R2 ∼ 0.9), we found that a 25% warming reduction at the district-level requires curtailing animal manure, nitrogen fertilizer, and water input by 8.5%, 12.9%, and 10.9%, respectively. These curtailments nearly double for a 50% mitigation scenario. Comparing our emissions with previous bottom-up studies (used as inputs in global climate models) revealed discrepancies in prior national figures. With top-down estimates, our emissions correlated positively, suggesting higher reliability. Including our new regionally validated data in global climate models may provide more accurate climate projections at the Indian and global scales.

由于洪水灌溉引起的厌氧条件,水稻种植会产生甲烷 (CH4),严重加剧全球变暖。虽然大多数研究使用的是国家排放因子(EFs),但我们的研究综合了印度(仅次于中国的第二大甲烷排放国)已发表的 726 项测量结果,制定了地区级水体特定排放因子,用于估算地区级排放量和变暖潜力。1966-2017 年间,受水稻面积和水系变化的影响,印度稻田的甲烷排放量从 3.7(3.4-4.1)兆吨增至 4.8(4.4-5.3)兆吨。同时,受畜禽粪便、化肥施用和水投入等管理措施的影响,地区级排放量增加了 930%,与之前的估计相比,准确地反映了地区差异。通过采用一种新型多输出随机森林减排模型(R2 ∼ 0.9),我们发现,要在地区层面减少 25% 的升温,需要将畜禽粪便、氮肥和水的投入量分别减少 8.5%、12.9% 和 10.9%。在减排 50% 的情况下,这些削减量几乎翻了一番。将我们的排放量与之前自下而上的研究(作为全球气候模型的输入)进行比较,发现之前的国家数据存在差异。与自上而下的估计相比,我们的排放量呈正相关,表明可靠性更高。将我们经过地区验证的新数据纳入全球气候模型,可以在印度和全球范围内提供更准确的气候预测。
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引用次数: 0
Permafrost Region Greenhouse Gas Budgets Suggest a Weak CO2 Sink and CH4 and N2O Sources, But Magnitudes Differ Between Top-Down and Bottom-Up Methods 永冻土区温室气体预算表明二氧化碳吸收较弱,甲烷和一氧化二氮来源较多,但自上而下法和自下而上法得出的结果存在差异
IF 5.4 2区 地球科学 Q1 ENVIRONMENTAL SCIENCES Pub Date : 2024-10-26 DOI: 10.1029/2023GB007969
G. Hugelius, J. Ramage, E. Burke, A. Chatterjee, T. L. Smallman, T. Aalto, A. Bastos, C. Biasi, J. G. Canadell, N. Chandra, F. Chevallier, P. Ciais, J. Chang, L. Feng, M. W. Jones, T. Kleinen, M. Kuhn, R. Lauerwald, J. Liu, E. López-Blanco, I. T. Luijkx, M. E. Marushchak, S. M. Natali, Y. Niwa, D. Olefeldt, P. I. Palmer, P. K. Patra, W. Peters, S. Potter, B. Poulter, B. M. Rogers, W. J. Riley, M. Saunois, E. A. G. Schuur, R. L. Thompson, C. Treat, A. Tsuruta, M. R. Turetsky, A.-M. Virkkala, C. Voigt, J. Watts, Q. Zhu, B. Zheng

Large stocks of soil carbon (C) and nitrogen (N) in northern permafrost soils are vulnerable to remobilization under climate change. However, there are large uncertainties in present-day greenhouse gas (GHG) budgets. We compare bottom-up (data-driven upscaling and process-based models) and top-down (atmospheric inversion models) budgets of carbon dioxide (CO2), methane (CH4) and nitrous oxide (N2O) as well as lateral fluxes of C and N across the region over 2000–2020. Bottom-up approaches estimate higher land-to-atmosphere fluxes for all GHGs. Both bottom-up and top-down approaches show a sink of CO2 in natural ecosystems (bottom-up: −29 (−709, 455), top-down: −587 (−862, −312) Tg CO2-C yr−1) and sources of CH4 (bottom-up: 38 (22, 53), top-down: 15 (11, 18) Tg CH4-C yr−1) and N2O (bottom-up: 0.7 (0.1, 1.3), top-down: 0.09 (−0.19, 0.37) Tg N2O-N yr−1). The combined global warming potential of all three gases (GWP-100) cannot be distinguished from neutral. Over shorter timescales (GWP-20), the region is a net GHG source because CH4 dominates the total forcing. The net CO2 sink in Boreal forests and wetlands is largely offset by fires and inland water CO2 emissions as well as CH4 emissions from wetlands and inland waters, with a smaller contribution from N2O emissions. Priorities for future research include the representation of inland waters in process-based models and the compilation of process-model ensembles for CH4 and N2O. Discrepancies between bottom-up and top-down methods call for analyses of how prior flux ensembles impact inversion budgets, more and well-distributed in situ GHG measurements and improved resolution in upscaling techniques.

北方永冻土中大量的土壤碳(C)和氮(N)储量在气候变化下很容易被重新移动。然而,目前的温室气体(GHG)预算存在很大的不确定性。我们比较了自下而上(数据驱动的放大模型和基于过程的模型)和自上而下(大气反演模型)的二氧化碳(CO2)、甲烷(CH4)和氧化亚氮(N2O)预算,以及 2000-2020 年整个地区的碳和氮的横向通量。自下而上的方法估计了所有温室气体从陆地到大气的较高通量。自下而上和自上而下的方法都显示了自然生态系统中的二氧化碳汇(自下而上:-29(-709,4);自上而下:-29(-709,4)):-29(-709,455),自上而下:-587(-862,-312)兆吨二氧化碳-年-1)和甲烷(CH4)的来源(自下而上:38(22,53)兆吨二氧化碳-年-1,自上而下:312兆吨甲烷-年-1):38 (22, 53), top-down:15 (11, 18) Tg CH4-C yr-1) 和 N2O (自下而上:0.7 (0.1, 0.2) Tg CO2-C yr-1) 的来源:0.7 (0.1, 1.3), top-down:0.09 (-0.19, 0.37) Tg N2O-N yr-1)。所有三种气体的综合全球变暖潜势(GWP-100)与中性无法区分。在较短的时间尺度上(GWP-20),该地区是温室气体净源,因为 CH4 在总强迫中占主导地位。北方森林和湿地的二氧化碳净吸收汇在很大程度上被火灾和内陆水域的二氧化碳排放以及湿地和内陆水域的甲烷排放所抵消,而一氧化二氮排放的贡献较小。未来研究的重点包括在基于过程的模型中表现内陆水域,以及汇编 CH4 和 N2O 的过程模型集合。自下而上和自上而下方法之间的差异要求分析先前的通量集合如何影响反演预算、更多和分布良好的原地温室气体测量,以及提高放大技术的分辨率。
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引用次数: 0
Intercropping Legumes Improves Long Term Productivity and Soil Carbon and Nitrogen Stocks in Sub-Saharan Africa 在撒哈拉以南非洲地区间作豆科植物可提高长期生产力和土壤碳氮储量
IF 5.4 2区 地球科学 Q1 ENVIRONMENTAL SCIENCES Pub Date : 2024-10-24 DOI: 10.1029/2024GB008159
Kathrin Fuchs, David Kraus, Tobias Houska, Michael Kermah, Edwin Haas, Ralf Kiese, Klaus Butterbach-Bahl, Clemens Scheer

Food, feed, and fiber production needs to increase to support demands of the growing population in Sub-Saharan Africa (SSA), while soil fertility continues to decline. Intercropping, the cultivation of two or more crop species on the same field, can provide yield benefits and is suggested to positively affect soil organic carbon (C) and nitrogen (N) stocks. This study uses the biogeochemical model system LandscapeDNDC with the objective to (a) represent maize-legume intercropping systems in different bioregions in SSA by simultaneously simulating both crops and their interactions and (b) assess long-term (20 years) impacts of intercropping under varying mineral fertilizer inputs (0–150 kg N ha−1 yr−1) on productivity as well as soil organic C and N stocks. We test LandscapeDNDC on 82 field data sets (site-year-treatment combinations) from 18 sites to represent yields and soil C/N dynamics of maize-legume intercropping systems. Using the model for long-term scenario simulations showed that intercropping allows to sustain productivity and to improve or maintain SOC stock in low or zero fertilizer systems if all residues are returned to the soil. In contrast, for sole-cropped maize systems, a decline in SOC stocks was simulated unless a minimum of 35 kg N ha−1 yr−1 of fertilizer was applied at full residue return. We conclude that intercropping using legumes alongside sufficient residue return allows for stabilizing long-term yields while avoiding SOC losses even with low fertilizer N inputs. Overall, our study confirms the potential of intercropping as a sustainable agricultural practice that could significantly contribute to food security in SSA.

撒哈拉以南非洲地区(SSA)需要提高粮食、饲料和纤维产量,以满足不断增长的人口需求,而土壤肥力却在持续下降。间作是指在同一块田地上种植两种或两种以上的作物,可以提高产量,并对土壤有机碳(C)和氮(N)储量产生积极影响。本研究使用生物地球化学模型系统 LandscapeDNDC,目的是:(a) 通过同时模拟两种作物及其相互作用,表现撒南非洲不同生物区域的玉米-豆类间作系统;(b) 评估在不同矿物肥料投入(0-150 千克氮公顷-1 年-1)条件下间作对生产力以及土壤有机碳和氮储量的长期(20 年)影响。我们在 18 个地点的 82 个田间数据集(地点-年份-处理组合)上对 LandscapeDNDC 进行了测试,以反映玉米-豆类间作系统的产量和土壤碳/氮动态。利用该模型进行的长期情景模拟显示,在低肥或零肥系统中,如果所有残留物都回归土壤,间作可以维持生产率,提高或保持 SOC 储量。相反,对于单作玉米系统,除非在全部残留物还田时施用至少 35 千克氮(公顷-1 年-1)的肥料,否则 SOC 储量会下降。我们的结论是,使用豆科植物进行间作套种,同时施用足够的残留物还田,即使施用较少的氮肥,也能稳定长期产量,同时避免 SOC 损失。总之,我们的研究证实了间作套种作为一种可持续农业实践的潜力,它能极大地促进撒哈拉以南非洲地区的粮食安全。
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引用次数: 0
Feedbacks From Young Permafrost Carbon Remobilization to the Deglacial Methane Rise 年轻冻土碳再移动对冰川期甲烷上升的反馈作用
IF 5.4 2区 地球科学 Q1 ENVIRONMENTAL SCIENCES Pub Date : 2024-10-22 DOI: 10.1029/2024GB008164
M. Sabino, Ö. Gustafsson, B. Wild, I. P. Semiletov, O. V. Dudarev, G. Ingrosso, T. Tesi

The abrupt warming events punctuating the Termination 1 (about 11.7–18 ka Before Present, BP) were marked by sharp rises in the concentration of atmospheric methane (CH4). The role of permafrost organic carbon (OC) in these rises is still debated, with studies based on top-down measurements of radiocarbon (14C) content of CH4 trapped in ice cores suggesting minimum contributions from old and strongly 14C-depleted permafrost OC. However, organic matter from permafrost can exhibit a continuum of 14C ages (contemporaneous to >50 ky). Here, we investigate the large-scale permafrost remobilization at the Younger Dryas-Preboreal transition (ca. 11.6 ka BP) using the sedimentary record deposited at the Lena River paleo-outlet (Arctic Ocean) to reflect permafrost destabilization in this vast drainage basin. Terrestrial OC was isolated from sediments and characterized geochemically measuring δ13C, Δ14C, and lignin phenol molecular fossils. Results indicate massive remobilization of relatively young (about 2,600 years) permafrost OC from inland Siberia after abrupt warming triggered severe active layer deepening. Methane emissions from this young fraction of permafrost OC contributed to the deglacial CH4 rise. This study stresses that underestimating permafrost complexities may affect our comprehension of the deglacial permafrost OC-climate feedback and helps understand how modern permafrost systems may react to rapid warming events, including enhanced CH4 emissions that would amplify anthropogenic climate change.

大气中甲烷(CH4)浓度的急剧上升标志着终止一期(距今约 11.7-18 ka)的突然变暖。永冻土有机碳(OC)在这些上升中的作用仍存在争议,根据对冰芯中捕获的 CH4 的放射性碳(14C)含量进行的自上而下的测量结果表明,来自古老的、严重贫化 14C 的永冻土有机碳的贡献最小。然而,来自永久冻土的有机物质可以表现出连续的 14C 年龄(同时代到 50 千年)。在此,我们利用沉积在勒拿河古出口(北冰洋)的沉积记录,研究了幼干纪-前寒武纪过渡时期(约 11.6 ka BP)的大规模永久冻土再移动,以反映这一巨大流域的永久冻土失稳。从沉积物中分离出陆地 OC,并通过测量 δ13C、Δ14C 和木质素酚分子化石对其进行地球化学特征描述。结果表明,在突然变暖引发活动层严重加深之后,西伯利亚内陆相对年轻(约 2,600 年)的永久冻土 OC 被大量重新移动。这部分年轻的永久冻土 OC 排放的甲烷导致了冰川期 CH4 的上升。这项研究强调,低估永久冻土的复杂性可能会影响我们对冰川期永久冻土 OC-气候反馈的理解,并有助于理解现代永久冻土系统如何对快速变暖事件做出反应,包括增加 CH4 排放,从而扩大人为气候变化。
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引用次数: 0
The Role of Acantharia in Southern Ocean Strontium Cycling and Carbon Export: Insights From Dissolved Strontium Concentrations and Seasonal Flux Patterns 南大洋锶循环和碳输出中的棘尾藻作用:溶解锶浓度和季节通量模式的启示
IF 5.4 2区 地球科学 Q1 ENVIRONMENTAL SCIENCES Pub Date : 2024-10-21 DOI: 10.1029/2024GB008227
Yaojia Sun, Cathryn A. Wynn-Edwards, Thomas W. Trull, Michael J. Ellwood

Dissolved strontium (Sr) concentrations from Southern Ocean water samples and Sr export fluxes from sediment trap moorings at 1,000 m were used to assess particulate organic carbon (POC) export associated with Acantharia for 2010, 2018, and 2020. The dissolved Sr data revealed a prominent vertical gradient with lower surface Sr concentrations depleted up to 1.5% relative to deep waters. A strong latitudinal surface gradient was observed, ranging from 86.8 μmol kg−1 near the northern end to 88.0 μmol kg−1 near the southern end of a transect through the Australian sector of the Southern Ocean. The vertical and latitudinal gradients are associated with celestite (SrSO4) precipitation by Acantharia and subsequent export to depth. Seasonal variability in Sr export fluxes can be large, particularly during intense events in summer, and reaches a maximum of 11.7 mmol Sr m−2 yr−1, contributing up to 7% of the POC export flux. The coincidence of Sr flux with the second peak of POC export flux implies an association of Acantharia biomass with summertime productivity.

利用南大洋水样中的溶解锶(Sr)浓度和 1,000 米处沉积物捕集锚系设备的 Sr 出口通量,评估了 2010 年、2018 年和 2020 年与棘尾藻有关的颗粒有机碳(POC)出口情况。溶解态 Sr 数据揭示了一个显著的垂直梯度,相对于深海而言,较低的表层 Sr 浓度消耗高达 1.5%。在穿越南大洋澳大利亚部分的横断面上,观察到了强烈的纬度表面梯度,从靠近北端的 86.8 μmol kg-1 到靠近南端的 88.0 μmol kg-1。垂直梯度和纬度梯度与棘尾藻沉淀天青石(SrSO4)并随后向深海输出有关。锶输出通量的季节变化很大,尤其是在夏季的强烈事件期间,最大可达 11.7 mmol Sr m-2 yr-1,占 POC 输出通量的 7%。锶通量与 POC 出口通量的第二个峰值相吻合,这意味着棘尾藻的生物量与夏季生产力有关。
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引用次数: 0
Significance of Urea in Sustaining Nitrite Production by Ammonia Oxidizers in the Oligotrophic Ocean 尿素在维持寡营养海洋中氨氧化剂产生亚硝酸盐方面的意义
IF 5.4 2区 地球科学 Q1 ENVIRONMENTAL SCIENCES Pub Date : 2024-10-16 DOI: 10.1029/2023GB007996
Xianhui S. Wan, Hua-Xia Sheng, Hui Shen, Wenbin Zou, Jin-Ming Tang, Wei Qin, Minhan Dai, Shuh-Ji Kao, Bess B. Ward

Nitrification, the stepwise oxidation of ammonia to nitrate via nitrite, is a key process in the marine nitrogen cycle. Reported nitrite oxidation rates frequently exceed ammonia oxidation rates below the euphotic zone, raising the fundamental question of whether the two steps are balanced and if alternative sources contribute to nitrite production in the dark ocean. Here we present vertically resolved profiles of ammonia, urea, and nitrite oxidation rates and their kinetic traits in the oligotrophic Subtropical North Pacific. Our results show active urea-derived nitrogen oxidation (urea-N oxidation) in the presence of experimental ammonium amendment, suggesting direct urea utilization. The depth-integrated rates of urea-N oxidation and ammonia oxidation are comparable, demonstrating that urea-N oxidation is a significant source of nitrite. The additional nitrite from urea-N oxidation helps to balance the two steps of nitrification in our study region. Nitrifiers exhibit high affinity for their substrates, and the apparent half-saturation constants for ammonia and nitrite oxidation decrease with depth. The apparent half-saturation constant for urea-N oxidation is higher than that for ammonia oxidation and shows no clear vertical trend. Such kinetic traits may account for the relatively higher urea concentration than ammonium concentration in the ocean's interior. Moreover, a compilation of our results and reported data shows a trend of increased urea-N oxidation relative to ammonia oxidation from the eutrophic coastal zone to the oligotrophic open ocean. This trend reveals a substrate-dependent biogeographic distribution of urea-N oxidation across marine environments and provides new information on the balance and flux of the marine nitrification process.

硝化作用是氨通过亚硝酸盐逐步氧化成硝酸盐的过程,是海洋氮循环的一个关键过程。据报道,亚硝酸盐氧化率经常超过极光带以下的氨氧化率,这就提出了一个根本性问题:这两个步骤是否平衡,是否有其他来源促成了暗海中亚硝酸盐的产生。在这里,我们展示了低营养亚热带北太平洋氨、尿素和亚硝酸盐氧化率的垂直分辨率剖面及其动力学特征。我们的研究结果表明,在实验性铵添加剂存在的情况下,尿素衍生氮氧化(脲-氮氧化)非常活跃,这表明尿素被直接利用。脲-氮氧化和氨氧化的深度整合速率相当,表明脲-氮氧化是亚硝酸盐的重要来源。在我们的研究区域,脲-N 氧化产生的额外亚硝酸盐有助于平衡硝化的两个步骤。硝化细菌对底物的亲和力很强,氨氧化和亚硝酸盐氧化的表观半饱和常数随深度的增加而降低。脲-N氧化的表观半饱和常数高于氨氧化,而且没有明显的垂直趋势。这种动力学特征可能是海洋内部尿素浓度高于氨浓度的原因。此外,综合我们的研究结果和已报道的数据,可以看出,从富营养化的沿岸带到低营养 化的开阔海域,脲-N 的氧化作用比氨的氧化作用有增加的趋势。这一趋势揭示了整个海洋环境中尿素-N 氧化作用的生物地理分布取决于基质,并为海洋硝化过程的平衡和通量提供了新的信息。
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引用次数: 0
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Global Biogeochemical Cycles
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