应对研究挑战,估算盐碱地恢复带来的蓝碳效益

IF 10.8 1区 环境科学与生态学 Q1 BIODIVERSITY CONSERVATION Global Change Biology Pub Date : 2024-10-10 DOI:10.1111/gcb.17526
Victoria G. Mason, Annette Burden, Graham Epstein, Lucy L. Jupe, Kevin A. Wood, Martin W. Skov
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引用次数: 0

摘要

Williamson 等人(2024 年)对我们在《全球变化生物学》(Global Change Biology)上发表的文章(Mason 等人,2024 年)中的一些内容提出了质疑,在这篇文章中,我们使用了来自 431 篇文章的数据来量化盐沼恢复带来的全球和区域碳效益。当沉积物中有机碳的主要来源是自生碳时,我们的方法(图 1a)可能会重复计算某些碳。Williamson 等人(2024 年)提出的另外两种方法(图 1b,c)也可以使用,但与我们的方法一样,无论测量的是自生碳积累还是自生和异生碳积累,都会高估或低估净碳积累。其中一种测量方法(图 1a)可能与 IPCC 方法一致(Kennedy 等人,2014 年),但可能不适合抵消或碳信用计划,因为在这些计划中应排除同源输入(Needelman 等人,2018 年)。碳通量中的净生态系统交换(NEE)仅包含自生碳,可通过涡度协方差(EC)测量(图 1c),揭示盐沼在仪器部署的时间尺度(年)内是二氧化碳源或吸收汇(±N2O 和 CH4)。然而,考虑到再矿化等较长期的沉积过程,仅对 NEE 的估计可能并不等同于较长 时间尺度(数十年)内的总碳积累(图 1b)(Lovett、Cole 和 Pace,2006 年)。因此,净排放系数本身(图 1c)可能会高估或低估碳储存。我们同意,区分自生碳和异生碳以及计算通过横向迁移交换的碳(见第 4.2 节)是盐沼碳领域下一步研究的关键。Williamson 等人(2024 年)建议以 EC 数据为基础计算 NEE 通量,但不包括室观测数据(图 1),因为它们的时间长度有限。我们同意,EC 在时间上更完整。然而,欧共体数据在空间上也很有限,而且存在区域偏差,因此无法进行全球分析。我们使用了一系列方法进行温室气体通量观测,包括静态(不透明或透明)室和短期或季节性欧共体观测。Shahan 等人(2022 年)的研究表明,将导电率法和室法结合起来可改进对净碳通量的估算。我们利用大型数据集计算了全球碳储量,确定了空间变化的环境驱动因素,强调了当前的数据缺口,并讨论了对政策的影响。我们欢迎就我们得出的净通量估算进行讨论,但强调这只是更大规模分析的一个组成部分。在我们的全球综合分析中,我们使用的是受地理和时间限制的不完美数据集。没有十全十美的数据集;因此,每种解释都会有不同的优势和局限性。维多利亚-梅森(Victoria G. Mason):概念化、形式分析、调查、方法论、可视化、写作-原稿、写作-审阅和编辑。Annette Burden:概念化、资金获取、方法论、可视化、写作--原稿、写作--审阅和编辑。Graham Epstein:构思、写作--审阅和编辑。Lucy L. Jupe:概念化、可视化、写作--审阅和编辑。Kevin A. Wood:概念化、写作--审阅和编辑。Martin W. Skov:概念化、方法学、监督、可视化、写作-原稿、写作-审阅和编辑。作者声明无利益冲突。本文是对威廉姆森等人的信件的回应,https://doi.org/10.1111/gcb.17525,该信件与梅森等人的论文有关,https://doi.org/10.1111/gcb.16943。
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Navigating Research Challenges to Estimate Blue Carbon Benefits From Saltmarsh Restoration

Williamson et al. (2024) queried elements of our article in Global Change Biology (Mason et al. 2024), where we used data from 431 articles to quantify global and regional carbon benefits from saltmarsh restoration.

The first query concerns the risk of double counting some carbon through including CO2 flux within net flux calculations. Some carbon could be double counted with our approach (Figure 1a) when the major source of organic carbon to the sediment is autochthonous. Two other approaches proposed by Williamson et al. (2024) (Figure 1b,c) could be used, but, like ours, over- or underestimate net carbon accumulation, whether the measure is of autochthonous or both autochthonous and allochthonous C accumulation. One measure (Figure 1a) may be consistent with IPCC methodology (Kennedy et al. 2014), although can be inappropriate for offsetting or carbon credit schemes where allochthonous inputs should be excluded (Needelman et al. 2018). Net ecosystem exchange (NEE) in C flux incorporates only autochthonous carbon and can be measured by eddy covariance (EC) (Figure 1c), revealing saltmarshes to be a CO2 source or sink (±N2O and CH4) over the timescale of instrument deployment (years). However, NEE-only estimates may not equate to total carbon accumulation over longer timescales (decades) (Figure 1b) (Lovett, Cole, and Pace 2006), given longer term sediment processes such as remineralisation. Thus, NEE on its own (Figure 1c) can over/underestimate carbon storage. We agree that distinguishing between autochthonous and allochthonous carbon and accounting for carbon exchanged through lateral transport (see section 4.2) are critical next steps in the field of saltmarsh carbon. However, scarcity in published data restricted our ability to account for these processes.

Williamson et al. (2024) suggest basing NEE flux calculations on EC data and excluding chamber-based observations (Figure 1) as their time durations are restricted. We agree that EC is more temporally complete. Yet, EC is also spatially scant and regionally biased, precluding any global analysis. We used GHG flux observations from a range of methodologies including static (opaque or transparent) chambers and EC done on a short-term or seasonal basis. Shahan et al. (2022) showed combining EC and chamber methods improved estimates of net carbon fluxes. Mayen et al. (2024) found that the absence of observations during inundated periods did not influence annual flux rates.

We utilised a large dataset to calculate global carbon stock, identify environmental drivers of spatial variation, highlight current data gaps and discuss implications for policy. We welcome discussion concerning the net flux estimate we produced, but underline that this is just one component of a much larger analysis. In our global synthesis, we worked with an imperfect data set subject to geographical and temporal limitations. There is no perfect data set; consequent interpretations will each have different strengths and limitations. As such, we acknowledge the limitations of our approach and work with what we have until we have well-parameterised models to predict C gains or losses across different contexts.

Victoria G. Mason: conceptualization, formal analysis, investigation, methodology, visualization, writing – original draft, writing – review and editing. Annette Burden: conceptualization, funding acquisition, methodology, visualization, writing – original draft, writing – review and editing. Graham Epstein: conceptualization, writing – review and editing. Lucy L. Jupe: conceptualization, visualization, writing – review and editing. Kevin A. Wood: conceptualization, writing – review and editing. Martin W. Skov: conceptualization, methodology, supervision, visualization, writing – original draft, writing – review and editing.

The authors declare no conflicts of interest.

This article is a Response to the Letter by Williamson et al, https://doi.org/10.1111/gcb.17525, which was related to the paper of Mason et al, https://doi.org/10.1111/gcb.16943.

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来源期刊
Global Change Biology
Global Change Biology 环境科学-环境科学
CiteScore
21.50
自引率
5.20%
发文量
497
审稿时长
3.3 months
期刊介绍: Global Change Biology is an environmental change journal committed to shaping the future and addressing the world's most pressing challenges, including sustainability, climate change, environmental protection, food and water safety, and global health. Dedicated to fostering a profound understanding of the impacts of global change on biological systems and offering innovative solutions, the journal publishes a diverse range of content, including primary research articles, technical advances, research reviews, reports, opinions, perspectives, commentaries, and letters. Starting with the 2024 volume, Global Change Biology will transition to an online-only format, enhancing accessibility and contributing to the evolution of scholarly communication.
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