{"title":"长期的人为干扰加速了地球最干旱生态系统中土壤碳的流失","authors":"Hua Zhang, Ganghua Li","doi":"10.1111/gcb.70489","DOIUrl":null,"url":null,"abstract":"<p>Drylands cover over 41% of Earth's terrestrial surface and support nearly 38% of the global population, yet they have long been overlooked in global carbon cycle assessments due to their low net primary productivity (Chen et al. <span>2024</span>). Despite this, drylands store substantial soil organic carbon (SOC), often deeply buried and stabilized by vegetation and microbial communities adapted to arid conditions. In hyperarid deserts, deep-rooted plants such as Alhagi sparsifolia create vertical SOC stratification, with labile particulate organic carbon (POC) near the surface and persistent mineral-associated organic carbon (MAOC) at depth (Zhao et al. <span>2025</span>). This deep carbon pool is a slow-cycling reservoir that can sequester carbon for centuries, making drylands potentially important carbon sinks despite low productivity. However, intensifying human disturbances, biomass harvesting, burning, and irrigation pose increasing risks to the stability of these carbon stocks (Ali and Xu <span>2025</span>; Chen et al. <span>2024</span>; Delcourt et al. <span>2025</span>). The fate of the more stable microbial-derived carbon and its mineral associations under chronic disturbance remains poorly understood.</p><p>Recent work by Gao et al. (<span>2025</span>), published in Global Change Biology, provides valuable new insights through a rare 16-year field experiment along the southern margin of the Taklimakan Desert, one of the world's driest and most fragile ecosystems. Their study applies disturbances mimicking local human activities, seasonal biomass harvest, fire, and artificial irrigation, to reveal how long-term anthropogenic pressure drives SOC loss. The study site, a desert–oasis transition zone, is stabilized by perennial shrubs like <i>Alhagi sparsifolia</i>, which also provide forage for local herders during spring and autumn harvests. Vegetation burning and artificial floodwater channeling are common disturbances whose impacts on SOC were unclear before this work.</p><p>Starting in 2008, Gao et al. (<span>2025</span>) applied five treatments annually: control (no disturbance), spring harvest, autumn harvest, fire, and irrigation simulating flood events. Each 30 × 50 m plot was buffered to prevent cross-contamination. This uncommon long-term, consistent disturbance experiment allowed a detailed investigation of chronic impacts in a hyperarid environment. In 2024, the team sampled plant biomass, litter, fine roots, and soils to 150 cm depth at six intervals. SOC was fractionated into POC (> 53 μm) and MAOC (< 53 μm). Plant-derived carbon was traced using lignin phenol biomarkers, and microbial-derived carbon quantified via amino sugars from fungal and bacterial residues. Soil mineralogy, enzyme activities, microbial biomass, and community composition from metagenomic sequencing were also measured, enabling a comprehensive mechanistic view of SOC dynamics.</p><p>Results showed consistent SOC depletion across all disturbance types. Total SOC declined by 13.2% relative to controls, with POC decreasing by 16.3% and MAOC suffering a striking 41.1% loss. The POC/MAOC ratio rose 46.2%, indicating destabilization: a shift from stable, mineral-protected carbon to a more labile, decomposition-prone pool. The 0–15 cm surface soil, rich in plant residues and weakly protected carbon, was most vulnerable, showing steep declines. Although deeper soils (> 100 cm) were less affected, significant losses occurred in microbial-derived carbon, the main stabilizer in subsoils. In absolute terms, disturbances removed an average of ~5.6 Mg C ha<sup>−1</sup> of SOC across the 0–150 cm profile, with losses reaching ~9 Mg C ha<sup>−1</sup> under autumn harvest and irrigation treatments. If extrapolated across the hyperarid margins of the Taklimakan (~100,000 km<sup>2</sup> of shrubland), this could translate into regional SOC losses on the order of 0.9–1.2 Pg C, suggesting potentially important implications for the global carbon cycle.</p><p>Not all disturbances impacted SOC equally. Autumn harvest and irrigation caused the greatest losses (~20%–21%), far exceeding spring harvest and fire. Autumn harvest likely removes biomass during a critical phase, reducing surface litter and fine root inputs needed to replenish POC. Irrigation introduced large water pulses, increasing leaching of dissolved organic carbon and promoting microbial conditions favoring rapid turnover over stabilization. Fire surprisingly had smaller net effects on SOC than in many forest biomes. In this hyperarid system, autumn burning left root systems mostly intact and sometimes enhanced post-fire germination. Ash inputs might contribute nutrients and undecomposed fragments, though benefits depend on context; in windy deserts, ash can be lost, and fire may increase erosion risk.</p><p>A key finding was the contrasting role of plant- and microbial-derived carbon by depth. Surface SOC variation correlated mainly with POC and plant carbon, while in the deepest layer (100–150 cm), microbial-derived carbon dominated. Disturbances reduced microbial carbon by 16.2%, linked to decreases in exchangeable calcium and noncrystalline iron/aluminum oxides, minerals critical for organic matter protection, and shifts in microbial communities. Fast-growing r-strategy bacteria (e.g., <i>Actinobacteria</i>, <i>Proteobacteria</i>) increased, while residue-rich fungi declined. Since fungal residues were almost four times more abundant than bacterial residues, this shift threatens long-term carbon stabilization.</p><p>The depletion of MAOC is concerning, as MAOC represents a slow-cycling, centuries-persistent carbon fraction; its loss could reduce soil's long-term carbon storage capacity. In low-productivity, hyperarid ecosystems, such losses may be difficult to reverse within feasible management timescales. The shift from MAOC to POC dominance suggests soils become more vulnerable to future losses, potentially triggering a self-reinforcing degradation cycle. Loss of vegetation exposes soils to wind erosion, reduces seed banks, and hampers recovery, accelerating SOC depletion. Methodologically, the study's 16-year duration, deep soil sampling, and integration of biochemical, mineralogical, and microbial data provide unprecedented mechanistic insights. Structural equation modeling revealed distinct disturbance pathways affecting SOC at different depths: direct litter removal and POC loss at the surface, and indirect impacts via mineral protection and microbial residues below. Such depth-specific understanding is critical for improving Earth system models' representation of SOC dynamics under disturbance.</p><p>However, some limitations remain. The experiment held disturbance intensity constant, preventing identification of threshold effects where SOC loss accelerates. Plots cover a small fraction of the desert–oasis interface, limiting broad extrapolation. The irrigation treatment simulated flood events but may not capture variability in natural floods. Combined or sequential disturbances were not tested, though these often co-occur in real landscapes and may interact in complex ways. These limitations mean that extrapolating results to larger regions must be done with caution: real-world disturbances vary in timing, frequency, and intensity, and interactions among them may amplify or dampen carbon loss. Thus, while the study provides invaluable mechanistic insight, the absolute magnitudes of loss at broader scales should be interpreted as indicative rather than predictive.</p><p>The implications of this study for land management are clear. First, autumn harvests should be minimized in fragile desert margins to protect topsoil carbon stocks. Second, artificial flooding should be reconsidered due to the potential for SOC leaching; if irrigation is necessary, smaller and more frequent applications may reduce harm. Although fire is less damaging than expected, it still poses erosion risks and should be tightly controlled. More broadly, subsurface SOC dynamics, especially microbial-derived carbon, must be incorporated into desertification control and global carbon accounting frameworks.</p><p>Perhaps most importantly, Gao et al. (<span>2025</span>) highlight that chronic, low-intensity disturbances can erode centuries-old carbon stocks in some of Earth's harshest environments. In hyperarid deserts, where organic matter accumulation is extremely limited, the tolerance for further loss is very low. This challenges the assumption that low-productivity drylands are inherently resilient to carbon depletion. As climate change intensifies and human pressures on drylands grow, these long-lived carbon reservoirs risk irreversible drawdown, fueling positive feedbacks that exacerbate global warming. Protecting them requires minimizing disturbances and embedding an understanding of depth-resolved SOC mechanisms in climate and land management policies. Gao et al. (<span>2025</span>) make it clear that in the driest places on Earth, every disturbance can contribute to carbon loss, and recovery of these carbon stocks may take centuries.</p><p><b>Hua Zhang:</b> conceptualization, writing – original draft, writing – review and editing. <b>Ganghua Li:</b> conceptualization, funding acquisition, project administration, supervision, writing – review and editing.</p><p>The authors declare no conflicts of interest.</p><p>This article is a Commentary on Gao et al. (<span>2025</span>) https://doi.org/10.1111/gcb.70423.</p>","PeriodicalId":175,"journal":{"name":"Global Change Biology","volume":"31 9","pages":""},"PeriodicalIF":12.0000,"publicationDate":"2025-09-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1111/gcb.70489","citationCount":"0","resultStr":"{\"title\":\"Long-Term Human Disturbance Accelerates Soil Carbon Loss in Earth's Driest Ecosystems\",\"authors\":\"Hua Zhang, Ganghua Li\",\"doi\":\"10.1111/gcb.70489\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p>Drylands cover over 41% of Earth's terrestrial surface and support nearly 38% of the global population, yet they have long been overlooked in global carbon cycle assessments due to their low net primary productivity (Chen et al. <span>2024</span>). Despite this, drylands store substantial soil organic carbon (SOC), often deeply buried and stabilized by vegetation and microbial communities adapted to arid conditions. In hyperarid deserts, deep-rooted plants such as Alhagi sparsifolia create vertical SOC stratification, with labile particulate organic carbon (POC) near the surface and persistent mineral-associated organic carbon (MAOC) at depth (Zhao et al. <span>2025</span>). This deep carbon pool is a slow-cycling reservoir that can sequester carbon for centuries, making drylands potentially important carbon sinks despite low productivity. However, intensifying human disturbances, biomass harvesting, burning, and irrigation pose increasing risks to the stability of these carbon stocks (Ali and Xu <span>2025</span>; Chen et al. <span>2024</span>; Delcourt et al. <span>2025</span>). The fate of the more stable microbial-derived carbon and its mineral associations under chronic disturbance remains poorly understood.</p><p>Recent work by Gao et al. (<span>2025</span>), published in Global Change Biology, provides valuable new insights through a rare 16-year field experiment along the southern margin of the Taklimakan Desert, one of the world's driest and most fragile ecosystems. Their study applies disturbances mimicking local human activities, seasonal biomass harvest, fire, and artificial irrigation, to reveal how long-term anthropogenic pressure drives SOC loss. The study site, a desert–oasis transition zone, is stabilized by perennial shrubs like <i>Alhagi sparsifolia</i>, which also provide forage for local herders during spring and autumn harvests. Vegetation burning and artificial floodwater channeling are common disturbances whose impacts on SOC were unclear before this work.</p><p>Starting in 2008, Gao et al. (<span>2025</span>) applied five treatments annually: control (no disturbance), spring harvest, autumn harvest, fire, and irrigation simulating flood events. Each 30 × 50 m plot was buffered to prevent cross-contamination. This uncommon long-term, consistent disturbance experiment allowed a detailed investigation of chronic impacts in a hyperarid environment. In 2024, the team sampled plant biomass, litter, fine roots, and soils to 150 cm depth at six intervals. SOC was fractionated into POC (> 53 μm) and MAOC (< 53 μm). Plant-derived carbon was traced using lignin phenol biomarkers, and microbial-derived carbon quantified via amino sugars from fungal and bacterial residues. Soil mineralogy, enzyme activities, microbial biomass, and community composition from metagenomic sequencing were also measured, enabling a comprehensive mechanistic view of SOC dynamics.</p><p>Results showed consistent SOC depletion across all disturbance types. Total SOC declined by 13.2% relative to controls, with POC decreasing by 16.3% and MAOC suffering a striking 41.1% loss. The POC/MAOC ratio rose 46.2%, indicating destabilization: a shift from stable, mineral-protected carbon to a more labile, decomposition-prone pool. The 0–15 cm surface soil, rich in plant residues and weakly protected carbon, was most vulnerable, showing steep declines. Although deeper soils (> 100 cm) were less affected, significant losses occurred in microbial-derived carbon, the main stabilizer in subsoils. In absolute terms, disturbances removed an average of ~5.6 Mg C ha<sup>−1</sup> of SOC across the 0–150 cm profile, with losses reaching ~9 Mg C ha<sup>−1</sup> under autumn harvest and irrigation treatments. If extrapolated across the hyperarid margins of the Taklimakan (~100,000 km<sup>2</sup> of shrubland), this could translate into regional SOC losses on the order of 0.9–1.2 Pg C, suggesting potentially important implications for the global carbon cycle.</p><p>Not all disturbances impacted SOC equally. Autumn harvest and irrigation caused the greatest losses (~20%–21%), far exceeding spring harvest and fire. Autumn harvest likely removes biomass during a critical phase, reducing surface litter and fine root inputs needed to replenish POC. Irrigation introduced large water pulses, increasing leaching of dissolved organic carbon and promoting microbial conditions favoring rapid turnover over stabilization. Fire surprisingly had smaller net effects on SOC than in many forest biomes. In this hyperarid system, autumn burning left root systems mostly intact and sometimes enhanced post-fire germination. Ash inputs might contribute nutrients and undecomposed fragments, though benefits depend on context; in windy deserts, ash can be lost, and fire may increase erosion risk.</p><p>A key finding was the contrasting role of plant- and microbial-derived carbon by depth. Surface SOC variation correlated mainly with POC and plant carbon, while in the deepest layer (100–150 cm), microbial-derived carbon dominated. Disturbances reduced microbial carbon by 16.2%, linked to decreases in exchangeable calcium and noncrystalline iron/aluminum oxides, minerals critical for organic matter protection, and shifts in microbial communities. Fast-growing r-strategy bacteria (e.g., <i>Actinobacteria</i>, <i>Proteobacteria</i>) increased, while residue-rich fungi declined. Since fungal residues were almost four times more abundant than bacterial residues, this shift threatens long-term carbon stabilization.</p><p>The depletion of MAOC is concerning, as MAOC represents a slow-cycling, centuries-persistent carbon fraction; its loss could reduce soil's long-term carbon storage capacity. In low-productivity, hyperarid ecosystems, such losses may be difficult to reverse within feasible management timescales. The shift from MAOC to POC dominance suggests soils become more vulnerable to future losses, potentially triggering a self-reinforcing degradation cycle. Loss of vegetation exposes soils to wind erosion, reduces seed banks, and hampers recovery, accelerating SOC depletion. Methodologically, the study's 16-year duration, deep soil sampling, and integration of biochemical, mineralogical, and microbial data provide unprecedented mechanistic insights. Structural equation modeling revealed distinct disturbance pathways affecting SOC at different depths: direct litter removal and POC loss at the surface, and indirect impacts via mineral protection and microbial residues below. Such depth-specific understanding is critical for improving Earth system models' representation of SOC dynamics under disturbance.</p><p>However, some limitations remain. The experiment held disturbance intensity constant, preventing identification of threshold effects where SOC loss accelerates. Plots cover a small fraction of the desert–oasis interface, limiting broad extrapolation. The irrigation treatment simulated flood events but may not capture variability in natural floods. Combined or sequential disturbances were not tested, though these often co-occur in real landscapes and may interact in complex ways. These limitations mean that extrapolating results to larger regions must be done with caution: real-world disturbances vary in timing, frequency, and intensity, and interactions among them may amplify or dampen carbon loss. Thus, while the study provides invaluable mechanistic insight, the absolute magnitudes of loss at broader scales should be interpreted as indicative rather than predictive.</p><p>The implications of this study for land management are clear. First, autumn harvests should be minimized in fragile desert margins to protect topsoil carbon stocks. Second, artificial flooding should be reconsidered due to the potential for SOC leaching; if irrigation is necessary, smaller and more frequent applications may reduce harm. Although fire is less damaging than expected, it still poses erosion risks and should be tightly controlled. More broadly, subsurface SOC dynamics, especially microbial-derived carbon, must be incorporated into desertification control and global carbon accounting frameworks.</p><p>Perhaps most importantly, Gao et al. (<span>2025</span>) highlight that chronic, low-intensity disturbances can erode centuries-old carbon stocks in some of Earth's harshest environments. In hyperarid deserts, where organic matter accumulation is extremely limited, the tolerance for further loss is very low. This challenges the assumption that low-productivity drylands are inherently resilient to carbon depletion. As climate change intensifies and human pressures on drylands grow, these long-lived carbon reservoirs risk irreversible drawdown, fueling positive feedbacks that exacerbate global warming. Protecting them requires minimizing disturbances and embedding an understanding of depth-resolved SOC mechanisms in climate and land management policies. Gao et al. (<span>2025</span>) make it clear that in the driest places on Earth, every disturbance can contribute to carbon loss, and recovery of these carbon stocks may take centuries.</p><p><b>Hua Zhang:</b> conceptualization, writing – original draft, writing – review and editing. <b>Ganghua Li:</b> conceptualization, funding acquisition, project administration, supervision, writing – review and editing.</p><p>The authors declare no conflicts of interest.</p><p>This article is a Commentary on Gao et al. 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引用次数: 0
摘要
旱地覆盖了地球陆地表面的41%以上,支持着全球近38%的人口,但由于其净初级生产力低,长期以来在全球碳循环评估中被忽视(Chen et al. 2024)。尽管如此,干旱地区储存了大量的土壤有机碳(SOC),这些有机碳通常被适应干旱条件的植被和微生物群落深深埋藏并稳定下来。在极度干旱的沙漠中,深根植物如疏叶桤木(Alhagi sparsifolia)形成垂直有机碳分层,表层附近有活性颗粒有机碳(POC),深层有持久性矿物相关有机碳(MAOC) (Zhao et al. 2025)。这个深层的碳库是一个缓慢循环的储存库,可以将碳封存几个世纪,使旱地成为潜在的重要碳汇,尽管生产力很低。然而,不断加剧的人类干扰、生物质采集、燃烧和灌溉对这些碳储量的稳定性构成了越来越大的风险(Ali and Xu 2025; Chen et al. 2024; Delcourt et al. 2025)。更稳定的微生物衍生碳及其矿物在慢性干扰下的命运仍然知之甚少。Gao等人(2025)最近发表在《全球变化生物学》(Global Change Biology)杂志上的研究,通过在塔克拉玛干沙漠南缘进行的罕见的16年野外实验,提供了有价值的新见解。塔克拉玛干沙漠是世界上最干旱、最脆弱的生态系统之一。他们的研究应用了模拟当地人类活动、季节性生物量收获、火灾和人工灌溉的干扰,以揭示长期人为压力是如何驱动SOC损失的。研究地点位于沙漠-绿洲的过渡地带,由多年生灌木(如Alhagi sparsifolia)稳定,这些灌木在春季和秋季收获期间也为当地牧民提供饲料。植被燃烧和人工泄洪是常见的干扰,对有机碳的影响在此之前还不清楚。从2008年开始,Gao等(2025)每年采用五种处理:控制(无干扰)、春收、秋收、火灾和模拟洪水事件的灌溉。每个30 × 50 m的地块缓冲以防止交叉污染。这种不寻常的长期、一致的干扰实验允许对超干旱环境中的慢性影响进行详细的调查。2024年,该团队分六个间隔对150厘米深的植物生物量、凋落物、细根和土壤进行了采样。SOC分为POC (> 53 μm)和MAOC (< 53 μm)。植物来源的碳使用木质素酚生物标志物进行追踪,微生物来源的碳通过真菌和细菌残留物中的氨基糖进行量化。此外,还测量了土壤矿物学、酶活性、微生物生物量和宏基因组测序的群落组成,从而对土壤有机碳动态进行了全面的机制观察。结果表明,在所有干扰类型中,SOC消耗是一致的。与对照组相比,总SOC下降了13.2%,其中POC下降了16.3%,MAOC下降了41.1%。POC/MAOC比值上升了46.2%,表明不稳定:从稳定的、受矿物保护的碳池转向更不稳定的、易于分解的碳池。0 ~ 15 cm表层土壤,植物残体丰富,保护碳较弱,最脆弱,下降幅度较大。虽然深层土壤(100厘米)受影响较小,但微生物衍生的碳(底土的主要稳定剂)损失显著。从绝对值上看,在0 ~ 150 cm剖面上,干扰平均减少了~5.6 Mg C ha - 1的有机碳,在秋收和灌溉处理下,损失达到~9 Mg C ha - 1。如果在塔克拉玛干的极度干旱边缘(约100,000平方公里的灌木丛)外推,这可能转化为0.9-1.2 Pg C的区域有机碳损失,这可能对全球碳循环产生重要影响。并非所有干扰对SOC的影响都是一样的。秋收和灌溉造成的损失最大(~20% ~ 21%),远远超过春收和火害。秋收可能会在关键阶段去除生物量,减少补充POC所需的地表凋落物和细根输入。灌溉引入了大的水脉冲,增加了溶解有机碳的浸出,促进了有利于快速周转而不是稳定的微生物条件。令人惊讶的是,与许多森林生物群落相比,火灾对有机碳的净影响较小。在这个极度干旱的系统中,秋季燃烧使根系基本完好无损,有时还能促进火后萌发。灰烬输入可能提供营养和未分解的碎片,但效益取决于环境;在多风的沙漠中,灰烬可能会流失,火灾可能会增加侵蚀的风险。一个关键的发现是植物碳和微生物碳在深度上的不同作用。表层有机碳变化主要与POC和植物碳相关,而最深层(100 ~ 150 cm)以微生物碳为主。干扰使微生物碳减少了16%。 2%,与可交换钙和非结晶铁/铝氧化物(对有机物保护至关重要的矿物质)的减少以及微生物群落的变化有关。快速生长的r策略细菌(如放线菌、变形菌)增加,而富含残留物的真菌减少。由于真菌残留物几乎是细菌残留物的四倍,这种转变威胁到长期的碳稳定。MAOC的消耗令人担忧,因为MAOC代表一种缓慢循环的、持续数世纪的碳组分;它的流失可能会降低土壤的长期碳储存能力。在低生产力、极度干旱的生态系统中,这种损失可能难以在可行的管理时间尺度内扭转。从MAOC主导向POC主导的转变表明,土壤更容易受到未来损失的影响,可能引发一个自我强化的退化循环。植被的丧失使土壤暴露于风蚀,减少了种子库,阻碍了恢复,加速了有机碳的消耗。在方法上,该研究持续了16年,进行了深度土壤采样,并整合了生化、矿物学和微生物数据,提供了前所未有的机制见解。结构方程模型揭示了影响不同深度有机碳的不同干扰途径:表层的直接凋落物清除和POC损失,以及表层的矿物保护和微生物残留的间接影响。这种深度特定的理解对于改善地球系统模型对扰动下有机碳动力学的表征至关重要。然而,仍然存在一些限制。实验保持干扰强度恒定,防止识别加速SOC损失的阈值效应。地块覆盖了沙漠-绿洲界面的一小部分,限制了广泛的推断。灌溉处理模拟洪水事件,但可能无法捕捉自然洪水的变化。组合或连续的干扰没有被测试,尽管这些经常在真实的景观中同时发生,并且可能以复杂的方式相互作用。这些限制意味着将结果外推到更大的区域时必须谨慎:现实世界的干扰在时间、频率和强度上各不相同,它们之间的相互作用可能会放大或抑制碳损失。因此,虽然这项研究提供了宝贵的机制见解,但在更广泛的尺度上,损失的绝对幅度应该被解释为指示性的,而不是预测性的。这项研究对土地管理的影响是显而易见的。首先,在脆弱的沙漠边缘应该尽量减少秋季收获,以保护表层土壤碳储量。其次,由于有机碳淋溶的可能性,应该重新考虑人工驱油;如果需要灌溉,更小更频繁的灌溉可以减少危害。尽管火灾的破坏性比预期的要小,但它仍然存在侵蚀风险,应该严格控制。更广泛地说,地下有机碳动态,特别是微生物碳源,必须纳入荒漠化控制和全球碳核算框架。也许最重要的是,Gao等人(2025)强调,在地球上一些最恶劣的环境中,慢性的、低强度的干扰可以侵蚀几个世纪以来的碳储量。在极度干旱的沙漠中,有机质积累极其有限,对进一步损失的容忍度非常低。这挑战了低生产力旱地对碳消耗具有内在弹性的假设。随着气候变化加剧和人类对旱地的压力增加,这些长期存在的碳库面临着不可逆转的减少风险,助长了加剧全球变暖的正反馈。保护它们需要最大限度地减少干扰,并在气候和土地管理政策中嵌入对深度解决的有机碳机制的理解。Gao等人(2025)明确指出,在地球上最干旱的地方,每一次干扰都可能导致碳损失,而这些碳储量的恢复可能需要几个世纪。张华:构思、撰写—初稿、撰写—审稿、编辑。Ganghua李:概念化、融资并购、项目管理、监督、写作——审查和编辑。作者声明无利益冲突。本文是对高等人(2025)https://doi.org/10.1111/gcb.70423的评论。
Long-Term Human Disturbance Accelerates Soil Carbon Loss in Earth's Driest Ecosystems
Drylands cover over 41% of Earth's terrestrial surface and support nearly 38% of the global population, yet they have long been overlooked in global carbon cycle assessments due to their low net primary productivity (Chen et al. 2024). Despite this, drylands store substantial soil organic carbon (SOC), often deeply buried and stabilized by vegetation and microbial communities adapted to arid conditions. In hyperarid deserts, deep-rooted plants such as Alhagi sparsifolia create vertical SOC stratification, with labile particulate organic carbon (POC) near the surface and persistent mineral-associated organic carbon (MAOC) at depth (Zhao et al. 2025). This deep carbon pool is a slow-cycling reservoir that can sequester carbon for centuries, making drylands potentially important carbon sinks despite low productivity. However, intensifying human disturbances, biomass harvesting, burning, and irrigation pose increasing risks to the stability of these carbon stocks (Ali and Xu 2025; Chen et al. 2024; Delcourt et al. 2025). The fate of the more stable microbial-derived carbon and its mineral associations under chronic disturbance remains poorly understood.
Recent work by Gao et al. (2025), published in Global Change Biology, provides valuable new insights through a rare 16-year field experiment along the southern margin of the Taklimakan Desert, one of the world's driest and most fragile ecosystems. Their study applies disturbances mimicking local human activities, seasonal biomass harvest, fire, and artificial irrigation, to reveal how long-term anthropogenic pressure drives SOC loss. The study site, a desert–oasis transition zone, is stabilized by perennial shrubs like Alhagi sparsifolia, which also provide forage for local herders during spring and autumn harvests. Vegetation burning and artificial floodwater channeling are common disturbances whose impacts on SOC were unclear before this work.
Starting in 2008, Gao et al. (2025) applied five treatments annually: control (no disturbance), spring harvest, autumn harvest, fire, and irrigation simulating flood events. Each 30 × 50 m plot was buffered to prevent cross-contamination. This uncommon long-term, consistent disturbance experiment allowed a detailed investigation of chronic impacts in a hyperarid environment. In 2024, the team sampled plant biomass, litter, fine roots, and soils to 150 cm depth at six intervals. SOC was fractionated into POC (> 53 μm) and MAOC (< 53 μm). Plant-derived carbon was traced using lignin phenol biomarkers, and microbial-derived carbon quantified via amino sugars from fungal and bacterial residues. Soil mineralogy, enzyme activities, microbial biomass, and community composition from metagenomic sequencing were also measured, enabling a comprehensive mechanistic view of SOC dynamics.
Results showed consistent SOC depletion across all disturbance types. Total SOC declined by 13.2% relative to controls, with POC decreasing by 16.3% and MAOC suffering a striking 41.1% loss. The POC/MAOC ratio rose 46.2%, indicating destabilization: a shift from stable, mineral-protected carbon to a more labile, decomposition-prone pool. The 0–15 cm surface soil, rich in plant residues and weakly protected carbon, was most vulnerable, showing steep declines. Although deeper soils (> 100 cm) were less affected, significant losses occurred in microbial-derived carbon, the main stabilizer in subsoils. In absolute terms, disturbances removed an average of ~5.6 Mg C ha−1 of SOC across the 0–150 cm profile, with losses reaching ~9 Mg C ha−1 under autumn harvest and irrigation treatments. If extrapolated across the hyperarid margins of the Taklimakan (~100,000 km2 of shrubland), this could translate into regional SOC losses on the order of 0.9–1.2 Pg C, suggesting potentially important implications for the global carbon cycle.
Not all disturbances impacted SOC equally. Autumn harvest and irrigation caused the greatest losses (~20%–21%), far exceeding spring harvest and fire. Autumn harvest likely removes biomass during a critical phase, reducing surface litter and fine root inputs needed to replenish POC. Irrigation introduced large water pulses, increasing leaching of dissolved organic carbon and promoting microbial conditions favoring rapid turnover over stabilization. Fire surprisingly had smaller net effects on SOC than in many forest biomes. In this hyperarid system, autumn burning left root systems mostly intact and sometimes enhanced post-fire germination. Ash inputs might contribute nutrients and undecomposed fragments, though benefits depend on context; in windy deserts, ash can be lost, and fire may increase erosion risk.
A key finding was the contrasting role of plant- and microbial-derived carbon by depth. Surface SOC variation correlated mainly with POC and plant carbon, while in the deepest layer (100–150 cm), microbial-derived carbon dominated. Disturbances reduced microbial carbon by 16.2%, linked to decreases in exchangeable calcium and noncrystalline iron/aluminum oxides, minerals critical for organic matter protection, and shifts in microbial communities. Fast-growing r-strategy bacteria (e.g., Actinobacteria, Proteobacteria) increased, while residue-rich fungi declined. Since fungal residues were almost four times more abundant than bacterial residues, this shift threatens long-term carbon stabilization.
The depletion of MAOC is concerning, as MAOC represents a slow-cycling, centuries-persistent carbon fraction; its loss could reduce soil's long-term carbon storage capacity. In low-productivity, hyperarid ecosystems, such losses may be difficult to reverse within feasible management timescales. The shift from MAOC to POC dominance suggests soils become more vulnerable to future losses, potentially triggering a self-reinforcing degradation cycle. Loss of vegetation exposes soils to wind erosion, reduces seed banks, and hampers recovery, accelerating SOC depletion. Methodologically, the study's 16-year duration, deep soil sampling, and integration of biochemical, mineralogical, and microbial data provide unprecedented mechanistic insights. Structural equation modeling revealed distinct disturbance pathways affecting SOC at different depths: direct litter removal and POC loss at the surface, and indirect impacts via mineral protection and microbial residues below. Such depth-specific understanding is critical for improving Earth system models' representation of SOC dynamics under disturbance.
However, some limitations remain. The experiment held disturbance intensity constant, preventing identification of threshold effects where SOC loss accelerates. Plots cover a small fraction of the desert–oasis interface, limiting broad extrapolation. The irrigation treatment simulated flood events but may not capture variability in natural floods. Combined or sequential disturbances were not tested, though these often co-occur in real landscapes and may interact in complex ways. These limitations mean that extrapolating results to larger regions must be done with caution: real-world disturbances vary in timing, frequency, and intensity, and interactions among them may amplify or dampen carbon loss. Thus, while the study provides invaluable mechanistic insight, the absolute magnitudes of loss at broader scales should be interpreted as indicative rather than predictive.
The implications of this study for land management are clear. First, autumn harvests should be minimized in fragile desert margins to protect topsoil carbon stocks. Second, artificial flooding should be reconsidered due to the potential for SOC leaching; if irrigation is necessary, smaller and more frequent applications may reduce harm. Although fire is less damaging than expected, it still poses erosion risks and should be tightly controlled. More broadly, subsurface SOC dynamics, especially microbial-derived carbon, must be incorporated into desertification control and global carbon accounting frameworks.
Perhaps most importantly, Gao et al. (2025) highlight that chronic, low-intensity disturbances can erode centuries-old carbon stocks in some of Earth's harshest environments. In hyperarid deserts, where organic matter accumulation is extremely limited, the tolerance for further loss is very low. This challenges the assumption that low-productivity drylands are inherently resilient to carbon depletion. As climate change intensifies and human pressures on drylands grow, these long-lived carbon reservoirs risk irreversible drawdown, fueling positive feedbacks that exacerbate global warming. Protecting them requires minimizing disturbances and embedding an understanding of depth-resolved SOC mechanisms in climate and land management policies. Gao et al. (2025) make it clear that in the driest places on Earth, every disturbance can contribute to carbon loss, and recovery of these carbon stocks may take centuries.
Hua Zhang: conceptualization, writing – original draft, writing – review and editing. Ganghua Li: conceptualization, funding acquisition, project administration, supervision, writing – review and editing.
The authors declare no conflicts of interest.
This article is a Commentary on Gao et al. (2025) https://doi.org/10.1111/gcb.70423.
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