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Unvegetated Tidal Flats: A Critical Yet Vulnerable Coastal Blue Carbon Sink 无植被的潮滩:一个关键但脆弱的沿海蓝色碳汇。
IF 12 1区 环境科学与生态学 Q1 BIODIVERSITY CONSERVATION Pub Date : 2026-01-23 DOI: 10.1111/gcb.70695
Yanping Wang, Changchun Li, Zhaoliang Peng, Jing Luo, Senlin Zhu, Yumeng Sun, Ruping Liu, Dongcheng Jiang, Xiangqian Zhou, Faming Wang

Unvegetated tidal flats, despite accounting for approximately 24.9% of global blue carbon ecosystem area, remain underrepresented in blue carbon budgets. Here, we synthesize data from 184 sites across 23 countries to quantify their carbon stocks, carbon accumulation rate (CAR) and greenhouse gas (GHG, CO2 and CH4) emissions. Our results reveal that tidal flats sequester 8.6 (4.5–9.9) Tg C yr−1 and store 1.2 (0.7–2.0) Pg C in the top meter of sediments, increasing global blue carbon estimates by 6%–17%. However, they simultaneously emit 0.073 Tg CH4 yr−1 (3.3 Tg CO2eq yr−1), 27.9% of the CH4 emissions from salt marshes, offsetting 14.1% (1.8%–20.4%) of their carbon sequestration benefits. Mudflats exhibit the highest carbon stocks and CO2 fluxes among different sediment types, primarily due to their abundant binding sites of fine-grained particles and stronger microbial activities. Both CAR and CH4 fluxes decline poleward, with tropical zone as hotspots. Our findings highlight the urgency of integrating tidal flats into climate mitigation strategies, particularly given their vulnerability to land-use changes and sea-level rise. Conservation efforts must balance carbon sequestration gains against CH4 trade-offs to optimize their climate regulation potential.

尽管未被植被覆盖的潮滩约占全球蓝碳生态系统面积的24.9%,但在蓝碳预算中的代表性仍然不足。在这里,我们综合了来自23个国家的184个站点的数据,量化了它们的碳储量、碳积累率(CAR)和温室气体(GHG、CO2和CH4)排放。我们的研究结果表明,潮滩在沉积物的顶部米中每年吸收8.6 (4.5-9.9)Tg C,储存1.2 (0.7-2.0)Pg C,使全球蓝碳估计值增加6%-17%。然而,它们同时每年排放0.073 Tg CH4 (3.3 Tg CO2eq每年-1),占盐沼CH4排放量的27.9%,抵消了14.1%(1.8%-20.4%)的固碳效益。泥滩在不同沉积物类型中碳储量和CO2通量最高,这主要是由于其丰富的细颗粒结合位点和较强的微生物活性。CAR和CH4通量均向极方向下降,热带为热点。我们的研究结果强调了将潮滩纳入气候缓解战略的紧迫性,特别是考虑到它们易受土地利用变化和海平面上升的影响。保护工作必须平衡碳固存收益与CH4的权衡,以优化其气候调节潜力。
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引用次数: 0
All Reforestation Methods Can Support Tropical Tree Diversity Recovery, but Drivers and Species Composition Vary 所有的再造林方法都可以支持热带树木多样性的恢复,但驱动因素和物种组成各不相同。
IF 12 1区 环境科学与生态学 Q1 BIODIVERSITY CONSERVATION Pub Date : 2026-01-23 DOI: 10.1111/gcb.70721
Laura E. Boeschoten, Joannès Guillemot, Juliano van Melis, Lourens Poorter, Ricardo R. Rodrigues, Frans Bongers, Paulo G. Molin, Marielos Peña-Claros, Vinicius C. Souza, Cássio A. P. Toledo, Patrick Faria Fernandes, Marcelo P. Ferreira, Angélica F. Resende, Laura H. P. Simões, Catherine Torres de Almeida, María Uriarte, Pedro H. S. Brancalion

Tropical landscapes are undergoing rapid transformation due to human activities and global change. Forest restoration has emerged as a key strategy to mitigate biodiversity loss and climate warming. However, a standardized assessment of how different restoration methods contribute to biodiversity recovery and conservation remains lacking. Here, we present the first comprehensive comparison of tree diversity restoration and the drivers of recovery across five main reforestation methods (naturally regenerating forests, biodiverse restoration plantings, short- and long-rotation tree monocultures, agroforests) relative to three reference systems (agropastoral lands, degraded and conserved forest remnants). Tree inventories were conducted in 519 plots (900 m2 each) across two forest types (rainforest and seasonally dry forest) in the Atlantic forest of São Paulo state, Brazil, encompassing over 39,000 trees and 869 species. We found that: (1) all reforestation methods except short-rotation monoculture plots supported tree diversity recovery. In the rainforest, conserved remnant plots maintained the highest average Shannon diversity (Hill 1 = 29 ± 14), while naturally regenerating forests and restoration plantings approached the diversity of degraded remnant plots (15 ± 5). In seasonally dry forest, biodiverse restoration plantings and agroforests reached diversity levels comparable to conserved remnants (15 ± 6). Additionally, (2) recovery was influenced by forest age, climate (water availability), soil fertility, and landscape context, though the relative importance of these factors varied by method. Climate and landscape context were more influential for recovery in naturally regenerating forests, while soil conditions played a greater role in biodiverse restoration plantings. Lastly, (3) species composition in naturally regenerating forests most closely resembled that of conserved remnants. Conversely, restoration plantings and agroforests exhibited high compositional overlap across sites, reducing overall species richness. Our findings underscore the wide variation in biodiversity outcomes among and within reforestation methods, emphasizing that goals and strategies must align with local conditions to maximize benefits in complex tropical landscapes.

由于人类活动和全球变化,热带景观正经历着快速的变化。森林恢复已成为缓解生物多样性丧失和气候变暖的关键战略。然而,对于不同的恢复方法如何促进生物多样性恢复和保护的标准化评估仍然缺乏。在此,我们首次全面比较了五种主要再造林方法(自然再生林、生物多样性恢复种植、短期和长期轮作树木单一栽培、混交林)相对于三种参考系统(农牧地、退化和保护森林残余物)的树木多样性恢复和恢复驱动因素。在巴西圣保罗州大西洋森林的两种森林类型(雨林和季节性干林)中,对519个样地(每个900平方米)进行了树木调查,包括39000多棵树和869个物种。结果表明:(1)除短期轮作单一栽培样地外,其他造林方式均有利于树木多样性恢复。在热带雨林中,被保护的残余样地Shannon多样性平均值最高(Hill 1 = 29±14),自然更新林和恢复植被的多样性平均值接近退化的残余样地(15±5)。在季节性干旱林中,生物多样性恢复植被和农林业的多样性水平与保留植被相当(15±6)。此外,(2)森林恢复受林龄、气候(水分有效性)、土壤肥力和景观背景的影响,尽管这些因素的相对重要性因方法而异。在自然更新的森林中,气候和景观背景对恢复的影响更大,而土壤条件对生物多样性恢复的影响更大。最后,(3)自然再生林的物种组成与保护残林最接近。相反,恢复植被和农林业在样地间表现出高度重叠,降低了总体物种丰富度。我们的研究结果强调了造林方法之间和内部生物多样性结果的广泛差异,强调了目标和战略必须与当地条件相一致,才能在复杂的热带景观中实现效益最大化。
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引用次数: 0
Recovering European River Invertebrate Communities Homogenize or Differentiate Depending on Anthropogenic Stress 恢复欧洲河流无脊椎动物群落的同质化或分化取决于人为压力。
IF 12 1区 环境科学与生态学 Q1 BIODIVERSITY CONSERVATION Pub Date : 2026-01-22 DOI: 10.1111/gcb.70716
Daniela Cortés-Guzmán, Diana E. Bowler, Marie Anne Eurie Forio, Peter Goethals, Ioannis Karaouzas, Ariane Moulinec, James S. Sinclair, Rudy Vannevel, Peter Haase, Ellen A. R. Welti

Biodiversity loss can lead to biotic homogenization, whereby local communities within a region become increasingly similar over time, resulting in simplified communities with reduced functionality. However, our understanding of whether alleviating anthropogenic stress can reverse homogenization and promote biotic differentiation (i.e., increasing dissimilarity) remains limited, partly because the effectiveness of conservation actions is often assessed only at the local scale (e.g., increases in local diversity). Here, we examined evidence for biotic differentiation in European river invertebrate communities, a system that has generally shown signs of local recovery. We analyzed 447 time series of river invertebrate communities from 1994 to 2023, spanning 48 river basins across 15 European countries. We then related trends in community similarity within each basin, measured as taxonomic and trait β-diversity, to spatial gradients of anthropogenic stress, including ecological quality (a proxy of general anthropogenic stress), air temperature increase, and land cover pressure. β-diversity trends were strongly mediated by anthropogenic stress levels, with communities in lower-stress basins showing differentiation, while those in higher-stress basins homogenized. In addition, we found that the direction of β-diversity change depended less on taxa or traits being gained or lost, and more on the identity of the traits involved, highlighting how trait composition mediates community responses to anthropogenic change. Specifically, additions promoted differentiation at lower stress levels but contributed to homogenization under conditions of higher stress, whereas subtractions exhibited the inverse pattern. Our results demonstrate that β-diversity responds asymmetrically to spatial variation in anthropogenic stress, with both homogenization and differentiation occurring within a system that is, overall, undergoing recovery. Recognizing the stress-dependent responses of β-diversity allows researchers and managers to more accurately assess conservation success and provide recommendations that promote long-term ecosystem structural and functional recovery.

生物多样性丧失可导致生物同质化,即一个区域内的地方群落随着时间的推移变得越来越相似,导致群落功能降低。然而,我们对减轻人为压力是否可以逆转同质化和促进生物分化(即增加差异性)的理解仍然有限,部分原因是保护行动的有效性通常仅在局部尺度上进行评估(例如,增加局部多样性)。在这里,我们研究了欧洲河流无脊椎动物群落生物分化的证据,这个系统通常显示出局部恢复的迹象。我们分析了1994年至2023年间447个河流无脊椎动物群落的时间序列,涵盖了15个欧洲国家的48个河流流域。然后,我们将每个流域内的群落相似性趋势(以分类和性状β-多样性衡量)与人为压力的空间梯度(包括生态质量(一般人为压力的代表)、气温升高和土地覆盖压力)联系起来。β-多样性趋势受人为压力水平的强烈调节,低压力盆地的群落呈现分化,而高压力盆地的群落呈现均一化趋势。此外,我们发现β-多样性变化的方向较少取决于分类群或性状的获得或丢失,而更多地取决于所涉及性状的身份,突出了性状组成如何调节群落对人为变化的响应。具体来说,在较低的应力水平下,添加促进了分化,而在较高的应力水平下,添加促进了均匀化,而减法则表现出相反的模式。我们的研究结果表明,β-多样性对人为压力的空间变化做出了不对称的响应,在一个总体上正在恢复的系统中,均质化和分化都发生了。认识到β-多样性的压力依赖性反应使研究人员和管理者能够更准确地评估保护的成功,并提供促进长期生态系统结构和功能恢复的建议。
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引用次数: 0
Activation Energy Is a Useful Proxy for Intrinsic Stability of Soil Organic Matter 活化能是表征土壤有机质固有稳定性的有效指标
IF 12 1区 环境科学与生态学 Q1 BIODIVERSITY CONSERVATION Pub Date : 2026-01-20 DOI: 10.1111/gcb.70714
Ekaterina Filimonenko, Yakov Kuzyakov
<p>We thank Alster et al. (<span>2026</span>) for raising the importance of activation energy (<i>E</i><sub>a</sub>) for soil organic matter (SOM) decomposition. We agree that describing organic matter decomposition only with <i>E</i><sub>a</sub> is a simplification of simultaneously ongoing parallel and sequential processes. To understand their combined effects on element fluxes and cycling, the cumulative result is crucial. Here, we respond to the three points raised by Alster et al. (<span>2026</span>) and show that the Arrhenius <i>E</i><sub>a</sub> is a useful proxy for experimental and theoretical applications.</p><p>We showed that <i>E</i><sub>a</sub> is independent of temperature, but the energy barrier to reach the <i>E</i><sub>a</sub> level decreases with increasing temperature (figure 1 in Filimonenko and Kuzyakov <span>2025</span>). The enzymatic reactions have temperature optima, above which the reaction rate decreases due to changes in enzyme heat capacity and denaturation (Schipper et al. <span>2014</span>). In contrast, the abiotic SOM oxidation continuously increases with temperature.</p><p>The divergence between the temperature effect on reaction rate based on a simplified approach (figure 2 in Filimonenko and Kuzyakov <span>2025</span>) and estimates from figure 1c in Alster et al. (<span>2026</span>) is significant solely with glucose addition because: (i) the calculated <i>k</i> reflects not only SOM decomposition, but is the weighted average between <i>k</i> of glucose decomposition and <i>k</i> of SOM decomposition; and (ii) the induced positive priming intensifies decomposition of other SOM pools compared to that without glucose. This supports our data by nearly identical <i>E</i><sub>a</sub> values without glucose addition and under temperatures below 25°C (figure 1b in Alster et al. <span>2026</span>).</p><p>We discussed the <i>E</i><sub>a</sub> for four processes of organic matter transformation (Filimonenko and Kuzyakov <span>2025</span>), but did not review their temperature sensitivity. The reactions with high <i>E</i><sub>a</sub> are especially sensitive to warming (Davidson and Janssens <span>2006</span>). Applying precise methods to assess temperature sensitivity (Hobbs et al. <span>2013</span>; Alster et al. <span>2016</span>, <span>2020</span>) is limited by complex calculations and analytical overload. Our simplification helps to generalize temperature sensitivity of SOM decomposition.</p><p>Assuming that <i>E</i><sub>a</sub> is not a good SOM stability metric (Alster et al. <span>2026</span>), we expect an absence of or a negative correlation between <i>E</i><sub>a</sub> of SOM obtained by TGA-DSC and <i>E</i><sub>a</sub> of CO<sub>2</sub> released by microbial mineralization of organic matter. To our knowledge, no such negative correlation has ever been obtained. The reverse is instead true: the <i>E</i><sub>a</sub> of the thermally labile SOM pools is well correlated with CO<sub>2</sub> respired by microorga
我们感谢Alster等人(2026)提高了活化能(Ea)对土壤有机质(SOM)分解的重要性。我们同意仅用Ea描述有机物分解是同时进行的平行和顺序过程的简化。要了解它们对元素通量和循环的综合影响,累积结果至关重要。在这里,我们回应了Alster等人(2026)提出的三点,并表明Arrhenius Ea是实验和理论应用的有用代理。
{"title":"Activation Energy Is a Useful Proxy for Intrinsic Stability of Soil Organic Matter","authors":"Ekaterina Filimonenko,&nbsp;Yakov Kuzyakov","doi":"10.1111/gcb.70714","DOIUrl":"10.1111/gcb.70714","url":null,"abstract":"&lt;p&gt;We thank Alster et al. (&lt;span&gt;2026&lt;/span&gt;) for raising the importance of activation energy (&lt;i&gt;E&lt;/i&gt;&lt;sub&gt;a&lt;/sub&gt;) for soil organic matter (SOM) decomposition. We agree that describing organic matter decomposition only with &lt;i&gt;E&lt;/i&gt;&lt;sub&gt;a&lt;/sub&gt; is a simplification of simultaneously ongoing parallel and sequential processes. To understand their combined effects on element fluxes and cycling, the cumulative result is crucial. Here, we respond to the three points raised by Alster et al. (&lt;span&gt;2026&lt;/span&gt;) and show that the Arrhenius &lt;i&gt;E&lt;/i&gt;&lt;sub&gt;a&lt;/sub&gt; is a useful proxy for experimental and theoretical applications.&lt;/p&gt;&lt;p&gt;We showed that &lt;i&gt;E&lt;/i&gt;&lt;sub&gt;a&lt;/sub&gt; is independent of temperature, but the energy barrier to reach the &lt;i&gt;E&lt;/i&gt;&lt;sub&gt;a&lt;/sub&gt; level decreases with increasing temperature (figure 1 in Filimonenko and Kuzyakov &lt;span&gt;2025&lt;/span&gt;). The enzymatic reactions have temperature optima, above which the reaction rate decreases due to changes in enzyme heat capacity and denaturation (Schipper et al. &lt;span&gt;2014&lt;/span&gt;). In contrast, the abiotic SOM oxidation continuously increases with temperature.&lt;/p&gt;&lt;p&gt;The divergence between the temperature effect on reaction rate based on a simplified approach (figure 2 in Filimonenko and Kuzyakov &lt;span&gt;2025&lt;/span&gt;) and estimates from figure 1c in Alster et al. (&lt;span&gt;2026&lt;/span&gt;) is significant solely with glucose addition because: (i) the calculated &lt;i&gt;k&lt;/i&gt; reflects not only SOM decomposition, but is the weighted average between &lt;i&gt;k&lt;/i&gt; of glucose decomposition and &lt;i&gt;k&lt;/i&gt; of SOM decomposition; and (ii) the induced positive priming intensifies decomposition of other SOM pools compared to that without glucose. This supports our data by nearly identical &lt;i&gt;E&lt;/i&gt;&lt;sub&gt;a&lt;/sub&gt; values without glucose addition and under temperatures below 25°C (figure 1b in Alster et al. &lt;span&gt;2026&lt;/span&gt;).&lt;/p&gt;&lt;p&gt;We discussed the &lt;i&gt;E&lt;/i&gt;&lt;sub&gt;a&lt;/sub&gt; for four processes of organic matter transformation (Filimonenko and Kuzyakov &lt;span&gt;2025&lt;/span&gt;), but did not review their temperature sensitivity. The reactions with high &lt;i&gt;E&lt;/i&gt;&lt;sub&gt;a&lt;/sub&gt; are especially sensitive to warming (Davidson and Janssens &lt;span&gt;2006&lt;/span&gt;). Applying precise methods to assess temperature sensitivity (Hobbs et al. &lt;span&gt;2013&lt;/span&gt;; Alster et al. &lt;span&gt;2016&lt;/span&gt;, &lt;span&gt;2020&lt;/span&gt;) is limited by complex calculations and analytical overload. Our simplification helps to generalize temperature sensitivity of SOM decomposition.&lt;/p&gt;&lt;p&gt;Assuming that &lt;i&gt;E&lt;/i&gt;&lt;sub&gt;a&lt;/sub&gt; is not a good SOM stability metric (Alster et al. &lt;span&gt;2026&lt;/span&gt;), we expect an absence of or a negative correlation between &lt;i&gt;E&lt;/i&gt;&lt;sub&gt;a&lt;/sub&gt; of SOM obtained by TGA-DSC and &lt;i&gt;E&lt;/i&gt;&lt;sub&gt;a&lt;/sub&gt; of CO&lt;sub&gt;2&lt;/sub&gt; released by microbial mineralization of organic matter. To our knowledge, no such negative correlation has ever been obtained. The reverse is instead true: the &lt;i&gt;E&lt;/i&gt;&lt;sub&gt;a&lt;/sub&gt; of the thermally labile SOM pools is well correlated with CO&lt;sub&gt;2&lt;/sub&gt; respired by microorga","PeriodicalId":175,"journal":{"name":"Global Change Biology","volume":"32 1","pages":""},"PeriodicalIF":12.0,"publicationDate":"2026-01-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1111/gcb.70714","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"146005661","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"环境科学与生态学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Arrhenius Activation Energy Is Not a Useful Predictor of Soil Organic Matter Transformation and Its Consequences for Global Warming 阿伦尼乌斯活化能不是土壤有机质转化及其对全球变暖影响的有效预测因子。
IF 12 1区 环境科学与生态学 Q1 BIODIVERSITY CONSERVATION Pub Date : 2026-01-20 DOI: 10.1111/gcb.70713
Charlotte J. Alster, Vickery L. Arcus, Louis A. Schipper
<p>We commend Filimonenko and Kuzyakov (<span>2025</span>) for addressing the complex issue of identifying rate-limiting steps in soil organic matter (SOM) decomposition. Reconciling the biotic and abiotic processes governing SOM transformation is essential for predicting soil carbon losses under warming. However, three assumptions in their analysis require reconsideration to ensure accurate interpretation.</p><p> <b>Activation energy and the free energy barrier</b> </p><p>The Arrhenius equation defines the ‘activation energy’ empirically as the energy barrier determining reaction rates (<span></span><math> <semantics> <mrow> <msub> <mi>E</mi> <mi>a</mi> </msub> </mrow> <annotation>$$ {E}_a $$</annotation> </semantics></math>; Equation 1). Eyring and Polyani provided the theoretical basis for this using statistical thermodynamics (Evans and Polanyi <span>1935</span>; Eyring <span>1935</span>), and <span></span><math> <semantics> <mrow> <msub> <mi>E</mi> <mi>a</mi> </msub> </mrow> <annotation>$$ {E}_a $$</annotation> </semantics></math> was superseded by ‘activation free energy’ or Gibbs free energy of activation (<span></span><math> <semantics> <mrow> <mo>∆</mo> <msup> <mi>G</mi> <mo>‡</mo> </msup> </mrow> <annotation>$$ Delta {G}^{ddagger } $$</annotation> </semantics></math>; Equation 2; Truhlar and Klippenstein <span>1996</span>). Gibbs free energy of activation incorporates the enthalpy (<span></span><math> <semantics> <mrow> <mo>∆</mo> <msup> <mi>H</mi> <mo>‡</mo> </msup> </mrow> <annotation>$$ Delta {H}^{ddagger } $$</annotation> </semantics></math>) and entropy (<span></span><math> <semantics> <mrow> <mo>∆</mo> <msup> <mi>S</mi> <mo>‡</mo> </msup> </mrow> <annotation>$$ Delta {S}^{ddagger } $$</annotation> </semantics></math>) of activation (<span></span><math> <semantics> <mrow> <mo>∆</mo> <msup> <mi>G</mi> <mo>‡</mo> </msup> <mo>=</mo
我们赞扬Filimonenko和Kuzyakov(2025)解决了识别土壤有机质(SOM)分解速率限制步骤的复杂问题。协调控制SOM转化的生物和非生物过程对于预测变暖下土壤碳损失至关重要。然而,他们分析中的三个假设需要重新考虑,以确保准确的解释。根据经验,Arrhenius方程将“活化能”定义为决定反应速率的能垒(E a $$ {E}_a $$;方程1)。Eyring和Polyani用统计热力学(Evans和Polanyi 1935;Eyring 1935),E a $$ {E}_a $$被“活化自由能”或吉布斯活化自由能(∆G‡$$ Delta {G}^{ddagger } $$;方程2;Truhlar and Klippenstein 1996)。吉布斯活化自由能包含焓(∆H‡$$ Delta {H}^{ddagger } $$)和熵(∆S‡$$ Delta {S}^{ddagger } $$)(∆G‡=∆H‡- T∆S‡$$ Delta {G}^{ddagger }=Delta {H}^{ddagger }-TDelta {S}^{ddagger } $$),明确地捕获了反应势垒的温度依赖性(T $$ T $$)。虽然Arrhenius方程表面上类似于Eyring方程(方程2和3),但∆S‡$$ Delta {S}^{ddagger } $$隐藏在指数前因子中(方括号,方程3)。因此,如果使用阿伦尼乌斯方程模拟温度依赖性,则必须报告ea $$ {E}_a $$和a $$ A $$(指前因子);单独的ea $$ {E}_a $$错误地表示了反应的总能垒,并且忽略了它对温度的依赖性。Filimonenko和Kuzyakov(2025)没有报告A $$ A $$,忽略了激活熵。他们认为,“熵变……由于值极低,可以忽略不计。”因此,焓的变化等于吉布斯能'的变化。这种假设是无效的。利用他们的模型数据(Filimonenko和Kuzyakov 2025中的图2),我们拟合了Eyring方程并计算了∆H‡$$ Delta {H}^{ddagger } $$ = 35 kJ mol−1和T∆S‡$$ TDelta {S}^{ddagger } $$ =−32.0 kJ mol−1(在25°C时;图1a),数值相当,与他们的说法相矛盾。 ∆S‡$$ Delta {S}^{ddagger } $$的重要性已经得到了很好的证实,生物相关反应显示出大量的∆S‡$$ Delta {S}^{ddagger } $$(例如,wolenden et al. 1998)。Filimonenko和Kuzyakov(2025)通过ln(速率)与1/T估算ea $$ {E}_a $$,由于忽略了温度最优值,因此无法很好地接近生化过程。Lloyd和Taylor(1994)表明,这种线性拟合不能充分描述土壤呼吸,并开发了一个经验方程,允许E a $$ {E}_a $$随温度变化,该方程现在被广泛使用。其他研究也类似地表明,E a $$ {E}_a $$与已建立的理论(例如,Sierra 2012)是温度相关的。假设E为常数a $$ {E}_a $$会引入系统误差。例如,在图1b中,Arrhenius对土壤呼吸的预测偏离了一个更好拟合的三次函数。两个模型在22°C相交,这表明固定的E a $$ {E}_a $$在一个狭窄的范围内似乎是足够的,但在37°C时,Arrhenius模型将呼吸速率低估了20%. This deviation nearly doubles when labile substrate is added (Figure 1c). Given the underlying motivation here is to accurately model soil respiration under warming, such deviations are important.Calculated E a $$ {E}_a $$ also strongly depends on the temperature range used for estimation. Restricting the temperature range to 8°C–30°C changed modelled E a $$ {E}_a $$ significantly (Figure 1b,c) (c.f., Alster et al. 2016). Relying on sparce, inconsistent temperature points make E a $$ {E}_a $$ estimates in Filimonenko and Kuzyakov (2025) highly sensitive and undermines the use of a constant activation energy. Temperature sensitivity of activation energy undermines its use as a stability metric of soil organic matter A central premise of Filimonenko and Kuzyakov (2025) is that E a $$ {E}_a $$ can serve as a pro
{"title":"Arrhenius Activation Energy Is Not a Useful Predictor of Soil Organic Matter Transformation and Its Consequences for Global Warming","authors":"Charlotte J. Alster,&nbsp;Vickery L. Arcus,&nbsp;Louis A. Schipper","doi":"10.1111/gcb.70713","DOIUrl":"10.1111/gcb.70713","url":null,"abstract":"&lt;p&gt;We commend Filimonenko and Kuzyakov (&lt;span&gt;2025&lt;/span&gt;) for addressing the complex issue of identifying rate-limiting steps in soil organic matter (SOM) decomposition. Reconciling the biotic and abiotic processes governing SOM transformation is essential for predicting soil carbon losses under warming. However, three assumptions in their analysis require reconsideration to ensure accurate interpretation.&lt;/p&gt;&lt;p&gt;\u0000 &lt;b&gt;Activation energy and the free energy barrier&lt;/b&gt;\u0000 &lt;/p&gt;&lt;p&gt;The Arrhenius equation defines the ‘activation energy’ empirically as the energy barrier determining reaction rates (&lt;span&gt;&lt;/span&gt;&lt;math&gt;\u0000 &lt;semantics&gt;\u0000 &lt;mrow&gt;\u0000 &lt;msub&gt;\u0000 &lt;mi&gt;E&lt;/mi&gt;\u0000 &lt;mi&gt;a&lt;/mi&gt;\u0000 &lt;/msub&gt;\u0000 &lt;/mrow&gt;\u0000 &lt;annotation&gt;$$ {E}_a $$&lt;/annotation&gt;\u0000 &lt;/semantics&gt;&lt;/math&gt;; Equation 1). Eyring and Polyani provided the theoretical basis for this using statistical thermodynamics (Evans and Polanyi &lt;span&gt;1935&lt;/span&gt;; Eyring &lt;span&gt;1935&lt;/span&gt;), and &lt;span&gt;&lt;/span&gt;&lt;math&gt;\u0000 &lt;semantics&gt;\u0000 &lt;mrow&gt;\u0000 &lt;msub&gt;\u0000 &lt;mi&gt;E&lt;/mi&gt;\u0000 &lt;mi&gt;a&lt;/mi&gt;\u0000 &lt;/msub&gt;\u0000 &lt;/mrow&gt;\u0000 &lt;annotation&gt;$$ {E}_a $$&lt;/annotation&gt;\u0000 &lt;/semantics&gt;&lt;/math&gt; was superseded by ‘activation free energy’ or Gibbs free energy of activation (&lt;span&gt;&lt;/span&gt;&lt;math&gt;\u0000 &lt;semantics&gt;\u0000 &lt;mrow&gt;\u0000 &lt;mo&gt;∆&lt;/mo&gt;\u0000 &lt;msup&gt;\u0000 &lt;mi&gt;G&lt;/mi&gt;\u0000 &lt;mo&gt;‡&lt;/mo&gt;\u0000 &lt;/msup&gt;\u0000 &lt;/mrow&gt;\u0000 &lt;annotation&gt;$$ Delta {G}^{ddagger } $$&lt;/annotation&gt;\u0000 &lt;/semantics&gt;&lt;/math&gt;; Equation 2; Truhlar and Klippenstein &lt;span&gt;1996&lt;/span&gt;). Gibbs free energy of activation incorporates the enthalpy (&lt;span&gt;&lt;/span&gt;&lt;math&gt;\u0000 &lt;semantics&gt;\u0000 &lt;mrow&gt;\u0000 &lt;mo&gt;∆&lt;/mo&gt;\u0000 &lt;msup&gt;\u0000 &lt;mi&gt;H&lt;/mi&gt;\u0000 &lt;mo&gt;‡&lt;/mo&gt;\u0000 &lt;/msup&gt;\u0000 &lt;/mrow&gt;\u0000 &lt;annotation&gt;$$ Delta {H}^{ddagger } $$&lt;/annotation&gt;\u0000 &lt;/semantics&gt;&lt;/math&gt;) and entropy (&lt;span&gt;&lt;/span&gt;&lt;math&gt;\u0000 &lt;semantics&gt;\u0000 &lt;mrow&gt;\u0000 &lt;mo&gt;∆&lt;/mo&gt;\u0000 &lt;msup&gt;\u0000 &lt;mi&gt;S&lt;/mi&gt;\u0000 &lt;mo&gt;‡&lt;/mo&gt;\u0000 &lt;/msup&gt;\u0000 &lt;/mrow&gt;\u0000 &lt;annotation&gt;$$ Delta {S}^{ddagger } $$&lt;/annotation&gt;\u0000 &lt;/semantics&gt;&lt;/math&gt;) of activation (&lt;span&gt;&lt;/span&gt;&lt;math&gt;\u0000 &lt;semantics&gt;\u0000 &lt;mrow&gt;\u0000 &lt;mo&gt;∆&lt;/mo&gt;\u0000 &lt;msup&gt;\u0000 &lt;mi&gt;G&lt;/mi&gt;\u0000 &lt;mo&gt;‡&lt;/mo&gt;\u0000 &lt;/msup&gt;\u0000 &lt;mo&gt;=&lt;/mo","PeriodicalId":175,"journal":{"name":"Global Change Biology","volume":"32 1","pages":""},"PeriodicalIF":12.0,"publicationDate":"2026-01-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1111/gcb.70713","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"146008403","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"环境科学与生态学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Stressor Combinations Shift Soil Microbial Communities From Rare to Unknown Taxa and Alter Genomic Strategies 胁迫因子组合将土壤微生物群落从罕见的类群转移到未知的类群并改变基因组策略
IF 12 1区 环境科学与生态学 Q1 BIODIVERSITY CONSERVATION Pub Date : 2026-01-20 DOI: 10.1111/gcb.70704
Shuxun Cheng, Xianjin Tang, Xing Huang, Yang Li, Shuyi Huang, Dan He, Eduardo Moreno-Jiménez, Jianming Xu, Matthias C. Rillig, Zhongmin Dai, Manuel Delgado-Baquerizo

Soil microorganisms constitute the largest portion of Earth's biodiversity. However, soil microorganisms are also highly sensitive to on-going global change, and the influence of an increasing number of stressors on common, rare, and unknown taxa across large environmental gradients remains virtually unknown. Here, we combined a large-scale spatial field survey across multiple different ecosystems and found that the diversity and abundance of soil rare taxa were significantly reduced under high environmental stressor number (i.e., a high number of stressors passing a 75% stressor threshold). Strikingly, the abundance of unknown soil taxa and unknown genes increased with increasing environmental stress number. We further identified the metagenome-assembled genomes (MAGs) that were considered as relatively common taxa using metagenomics. Compared to 9% of negative responders, 32% of common MAGs were resistant or positively responsive to multiple stress, displaying a reduced potential for cellular processes and an enhanced potential for environmental, genetic, and metabolic processes. Our study suggests that as stress increases, we would have less rare, but more unknown microorganisms and unique genomes of resistant common taxa, suggesting major changes in the soil microbiome in a world subjected to multiple global change stressors.

土壤微生物构成了地球生物多样性的最大部分。然而,土壤微生物对持续的全球变化也高度敏感,越来越多的压力源对大环境梯度上常见、罕见和未知分类群的影响几乎仍然未知。在此基础上,通过对不同生态系统的大尺度空间野外调查发现,高环境压力源数量(即超过75%的压力源阈值)显著降低了土壤稀有类群的多样性和丰度。随着环境胁迫数的增加,未知土壤分类群和未知基因的丰度显著增加。我们进一步使用宏基因组学鉴定了被认为是相对常见的分类群的宏基因组组装基因组(MAGs)。与9%的阴性应答者相比,32%的普通mag对多重应激有抵抗或积极反应,显示细胞过程的潜力降低,环境、遗传和代谢过程的潜力增强。我们的研究表明,随着压力的增加,我们将有更少的罕见微生物,但更多的未知微生物和抗性常见分类群的独特基因组,这表明在遭受多重全球变化压力的世界中,土壤微生物组发生了重大变化。
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引用次数: 0
Effects of Eutrophication and Warming on Lake Ecosystems 富营养化和变暖对湖泊生态系统的影响。
IF 12 1区 环境科学与生态学 Q1 BIODIVERSITY CONSERVATION Pub Date : 2026-01-20 DOI: 10.1111/gcb.70715
Erik Jeppesen, Haojie Su, Haijun Wang, Zhengwen Liu
<p>Lake ecosystems are presently seriously threatened by various global changes. Two of the main stressors are (1) enhanced nutrient input, that is, eutrophication due to a fast-increasing world population demanding higher agricultural production, inevitably leading to higher nutrient loss, and (2) global warming (Birk et al. <span>2020</span>). Warming and eutrophication interact with major implications for lake ecosystem structure and function (Jeppesen et al. <span>2010</span>). Different approaches have been used to elucidate the interactions between warming and eutrophication in lakes. One method is space-for-time substitution (SFTS), based on cross-comparisons of data sampled along climate (latitude or altitude) and land-use gradients (e.g., Meerhoff et al. <span>2012</span>). The strength of SFTS is that the biological assemblages present have had time to evolve and adapt to the climate in which they live. However, a potential weakness is that regional biogeographical constraints are not considered. An alternative is to analyze long-term time-series data from periods facing changes in nutrient loading and climate. Such data are free of biogeographical problems and may provide information on the changes to be expected in the short term. However, they cannot account for changes (e.g., in species assemblages, (micro)evolution and adaptation) that will occur in the longer term, and they are inherently affected by transient/resilient phenomena. While SFTS and time-series studies have yielded important information on warming and eutrophication effects on lake ecosystems, both methods struggle to efficiently disentangle the impacts of warming and nutrient loading and their interactions. Full factorial controlled mesocosms experiments are a way forward—conducted either at a single location or in parallel across latitudes, possibly followed by cross-system meta-analyses (Macaulay et al. <span>2025</span>).</p><p>Like several others (for references, see Birk et al. <span>2020</span>, Macaulay et al. <span>2025</span>), Marin et al. (<span>2025</span>) conducted a full-factorial, well-replicated (<i>n</i> = 6) mesocosm experiment including ambient conditions as a control, nutrient addition (eutrophication), a +4°C heating (warming), eutrophication as well as warming. However, their study stands out, as they elegantly assessed the response to these two stressors at four different ecological levels: community composition, size structure, trophic architecture (using stable isotopes), and ecosystem functioning (e.g., decomposition in litter bags and GHG concentrations). They predicted that the responses to eutrophication and warming would differ between the four ecological levels as follows: (i) nutrient addition would enhance bottom-up forces by significantly increasing the abundance of primary producers, primarily affecting functioning; (ii) warming would reduce top-down force by excluding large species and reducing predators' abundance, primarily affe
目前,湖泊生态系统受到各种全球性变化的严重威胁。两个主要的压力源是:(1)增加的养分投入,即富营养化,由于世界人口的快速增长要求更高的农业生产,不可避免地导致更高的养分损失;(2)全球变暖(Birk et al. 2020)。变暖和富营养化相互作用,对湖泊生态系统的结构和功能产生重大影响(Jeppesen et al. 2010)。不同的方法被用来阐明变暖和湖泊富营养化之间的相互作用。一种方法是空间-时间替代(SFTS),基于沿气候(纬度或海拔)和土地利用梯度采样数据的交叉比较(例如,Meerhoff等人,2012年)。SFTS的优势在于,存在的生物组合有时间进化和适应它们所生活的气候。然而,一个潜在的弱点是没有考虑区域生物地理限制。另一种选择是分析长期时间序列数据,这些数据来自面临营养负荷和气候变化的时期。这种数据不存在生物地理问题,可以提供关于短期内预期变化的信息。然而,它们不能解释将在较长期内发生的变化(例如物种组合、(微观)进化和适应),而且它们本质上受到瞬时/弹性现象的影响。虽然SFTS和时间序列研究已经提供了关于变暖和富营养化对湖泊生态系统影响的重要信息,但这两种方法都难以有效地理清变暖和养分负荷的影响及其相互作用。全因子控制的中观实验是一种向前的方法——在单一地点或跨纬度平行进行,可能随后进行跨系统荟萃分析(Macaulay et al. 2025)。与其他几个人一样(参考文献,请参见Birk et al. 2020, Macaulay et al. 2025), Marin et al.(2025)进行了全因子,充分复制(n = 6)的中观实验,包括环境条件作为对照,营养添加(富营养化),+4°C加热(增温),富营养化和增温。然而,他们的研究脱颖而出,因为他们在四个不同的生态水平上优雅地评估了对这两个压力源的反应:群落组成、大小结构、营养结构(使用稳定同位素)和生态系统功能(例如,凋落物袋中的分解和温室气体浓度)。他们预测,四个生态水平对富营养化和变暖的响应存在以下差异:(i)营养添加会通过显著增加初级生产者的丰度来增强自下而上的力量,主要影响功能;(ii)变暖将通过排除大型物种和减少捕食者的丰度来减少自上而下的作用力,主要影响群落组成;(iii)食物网结构(尺寸谱和营养结构)对这两种处理的反应相似,因为它整合了自下而上和自上而下的力量的变化。支持他们的前两个假设,他们发现对两种压力源的反应在生态水平上是不同的——在群落水平上,变暖超过了营养添加的影响,在生态系统水平上,反之亦然。因此,营养物质的增加,加上气候变暖,在所有生态水平上都引起了反应。他们还发现,由大小结构和营养结构描述的食物网代表了一个中间的生态水平,它对这两种处理都有孤立的反应——营养投入引起的生态系统功能的变化与食物网属性(大小结构和营养结构)的变化有关,但不一定与群落组成或多样性的变化有关。相反,群落组成和多样性的变化与规模结构的变化有关,但与生态系统功能无关。这表明,气候变暖引起的群落水平变化在生态系统水平上得到了补偿,食物网提供了对所有响应的更综合的概述。此外,作者还发现了群落组成与生态系统功能之间的不匹配:不同的类群可能导致相似的生态功能,而相似的群落可能导致不同的生态功能。例如,异养过程,如凋落叶分解,在对照和加热处理中是相似的,尽管在无脊椎动物群落中存在重要差异。Marin et al.(2025)的研究进一步证实了之前的实证和实验研究结果,即随着初级生产者丰度的增加(导致食物链长度的缩短),初级消费者(同时也是捕食者)转向杂食性行为。它还揭示了气候变暖增加了自上而下的控制,这在其他研究中也有发现,但远非所有研究都有。
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引用次数: 0
Congo Basin Carbon Cycle Responses to Global Change 刚果盆地碳循环对全球变化的响应。
IF 12 1区 环境科学与生态学 Q1 BIODIVERSITY CONSERVATION Pub Date : 2026-01-20 DOI: 10.1111/gcb.70688
Sarah Worden, Rong Fu, A. Anthony Bloom, Marijn Bauters, Hans Verbeeck, Temilola Fatoyinbo, Wannes Hubau, Lydie-Stella Koutika, Steve Kwatcho Kengdo, Sybryn L. Maes, Vincent Medjibe, Nicholas J. Russo, Sassan Saatchi, Le Bienfaiteur Sagang, Thomas B. Smith, Denis J. Sonwa, Pascal Boeckx, Elsa M. Ordway

The Congo Basin and its contiguous forests harbor globally significant carbon stocks, estimated at 65 gigatons of C (GtC) above and belowground. Despite rising temperatures and intensifying droughts, they have remained a carbon sink, albeit weak: 0.26–0.50 GtC yr.−1 carbon uptake since 1980. However, these forests' carbon stocks and fluxes, including gross primary productivity, respiration, net primary productivity, and riverine carbon transport, remain poorly quantified. This limits understanding of the region's role in the global carbon cycle, its vulnerability to environmental change, and its potential as a long-term carbon sink. We review and quantify Congo Basin and contiguous forest carbon stocks and fluxes and synthesize the current knowledge on how key global change drivers shape the region's carbon cycle. We find limited responses to long-term precipitation variability, but declining stocks and fluxes in response to long-term and increasing temperature and drought frequency. Land cover and land use changes, largely driven by small-scale agriculture, logging, and agro-industrial expansion, reduce carbon stocks, ecosystem structure and functioning, and animal-mediated ecosystem services. In contrast, large-scale savanna biomass burning delivers phosphorus and nitrogen to Congo Basin forests via cross-equatorial winds, providing additional nutrients and supporting carbon sequestration. In situ studies suggest that CO2 fertilization has increased intrinsic water-use efficiency, although its effects may be modulated by climate change, and its impacts on biomass accumulation remain uncertain. Legacy effects from historical land use and climate change likely shaped present-day vegetation structure, yet their relative influence is unclear. High-resolution carbon monitoring, improved remote sensing, and strengthened in situ measurement networks are needed to quantify the impacts of these key drivers and their interactions on the Central African carbon cycle. This is needed to inform conservation strategies and advance understanding of the region's future as a carbon sink under global change pressures.

刚果盆地及其邻近的森林蕴藏着全球重要的碳储量,估计地上和地下的碳储量为650亿吨。尽管气温上升和干旱加剧,它们仍然是一个碳汇,尽管很弱:自1980年以来,每年的碳吸收量为0.26-0.50 GtC。然而,这些森林的碳储量和通量,包括总初级生产力、呼吸、净初级生产力和河流碳运输,仍然缺乏量化。这限制了对该地区在全球碳循环中的作用、其对环境变化的脆弱性以及其作为长期碳汇的潜力的理解。我们回顾和量化了刚果盆地和邻近的森林碳储量和通量,并综合了目前关于全球变化驱动因素如何塑造该地区碳循环的知识。我们发现对长期降水变率的响应有限,但对长期和不断增加的温度和干旱频率的响应是不断下降的储量和通量。土地覆盖和土地利用变化主要由小规模农业、伐木和农业工业扩张驱动,减少了碳储量、生态系统结构和功能以及动物介导的生态系统服务。相比之下,大规模的热带稀树草原生物质燃烧通过穿越赤道的风向刚果盆地森林输送磷和氮,提供额外的营养物质并支持碳固存。实地研究表明,CO2施肥提高了内在的水利用效率,尽管其影响可能受到气候变化的调节,而且其对生物量积累的影响仍不确定。历史土地利用和气候变化的遗留效应可能塑造了当今的植被结构,但它们的相对影响尚不清楚。要量化这些关键驱动因素及其相互作用对中非碳循环的影响,需要高分辨率碳监测、改进遥感和加强现场测量网络。这是为保护战略提供信息和促进对该地区未来在全球变化压力下作为碳汇的理解所必需的。
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引用次数: 0
Long-Term Records Reveal Temperature-Driven Nutrient Limitation and Predict Intensified Algal Blooms in Global Lakes 长期记录揭示了温度驱动的营养限制并预测了全球湖泊中藻华的加剧
IF 12 1区 环境科学与生态学 Q1 BIODIVERSITY CONSERVATION Pub Date : 2026-01-20 DOI: 10.1111/gcb.70719
Chuanqiao Zhou, Qiulin Xu, Ruoyu Jia, Zhihui Zhang, Xiaoguang Xu, Huazu Liu, Wenpeng Zhao, Erhu Du, Guoxiang Wang, Hideyuki Doi, Jianjun Wang, Tsuyoshi Kinouchi, Lian Feng

Harmful algal blooms (HABs) are an escalating global threat to aquatic ecosystems, reducing biodiversity, degrading water quality, and compromising human health. Climate-driven warming and excessive nutrient inputs are key drivers of HABs in global lakes. However, as nutrient reduction strategies gain traction, the relative contributions of rising water temperatures and nutrient enrichment remain unclear. Here, we compiled a dataset spanning 40 years from 156 lakes worldwide and analyzed the nonlinear response relationship between chlorophyll-a (Chl-a) and water temperature using a combination of empirical mode decomposition (EMD) and a random forest (RF) model. EMD demonstrated strong adaptability in extracting long-term stable signals from non-stationary records, revealing that over 40% of the lakes are eutrophic, with substantial spatial heterogeneity in HAB intensity; mean Chl-a concentrations reached as high as 26 μg L−1 in tropical regions. As warming continues, water temperature emerges as a progressively stronger driver of HABs, surpassing the influences of nutrient availability and stoichiometric balance. Rising water temperatures diminish the reliance of HABs on nutrient availability, while the nitrogen-to-phosphorus ratio consistently explains variation in Chl-a concentrations throughout the warming process. Furthermore, RF-based scenario projections indicate that under current warming and nutrient scenarios, the mean annual Chl-a concentrations of global lakes are projected to rise to 17.7 μg L−1 under RCP 4.5 and 18.4 μg L−1 under RCP 8.5 by the end of the 21st century. These findings highlight the urgent need to incorporate temperature effects into lake HAB management strategies.

有害藻华(HABs)对水生生态系统的全球威胁不断升级,减少了生物多样性,降低了水质,危害了人类健康。气候驱动的变暖和过多的养分输入是全球湖泊中有害藻华的主要驱动因素。然而,随着营养物减少策略的实施,水温上升和营养物富集的相对贡献仍不清楚。本文利用全球156个湖泊40年的数据集,结合经验模态分解(EMD)和随机森林(RF)模型,分析了叶绿素-a (Chl-a)与水温的非线性响应关系。EMD在从非平稳记录中提取长期稳定信号方面表现出较强的适应性,表明40%以上的湖泊富营养化,赤潮强度具有明显的空间异质性;热带地区平均Chl-a浓度高达26 μg L−1。随着气候持续变暖,水温逐渐成为有害藻华的驱动因素,超过了养分有效性和化学计量平衡的影响。水温上升减少了有害藻华对养分有效性的依赖,而氮磷比一致地解释了整个变暖过程中Chl-a浓度的变化。此外,基于rf的情景预估表明,在当前的增温和营养物情景下,到21世纪末,全球湖泊的年平均Chl-a浓度在RCP 4.5和RCP 8.5情景下分别上升到17.7和18.4 μ L−1。这些发现强调了将温度效应纳入湖泊赤潮管理策略的迫切需要。
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引用次数: 0
Fungal Panzootic Increasingly Threatens Temperate Amphibian Species While Impact Has Stabilised in Equatorial Regions 真菌流行性疾病日益威胁温带两栖动物物种,而对赤道地区的影响已趋于稳定。
IF 12 1区 环境科学与生态学 Q1 BIODIVERSITY CONSERVATION Pub Date : 2026-01-19 DOI: 10.1111/gcb.70712
Luke E. B. Goodyear, Deanna H. Olson, Kathryn L. Ronnenberg, Jaime Bosch, Daniel Pincheira-Donoso

Global amphibian declines outpace the loss of most organisms on Earth. The panzootic fungal disease chytridiomycosis, caused by Batrachochytrium dendrobatidis (Bd), is widely regarded as a predominant driver behind amphibian biodiversity erosion. However, a comprehensive global-scale analysis of the relationship between Bd and extinction risk remains lacking. Using a global database of Bd-detections and IUCN Red List extinction risk, we show that current amphibian declines are associated with Bd in temperate regions only, whereas historical analyses reveal a past peak of Bd-related declines across more equatorial areas during 1980–2004, that has diminished in intensity in recent decades (2004–2020). In contrast, temperate species show a lack of Bd-related declines during 1980–2004 but significant declines are currently ongoing. We suggest that the shorter activity seasons in temperate regions may have acted as ‘natural lockdowns’ that delayed the annihilating effects of Bd in susceptible species. Conversely, year-round activity in more amphibian-dense, equatorial areas may have triggered a faster transition into post-epizootic dynamics, characterised by a continuous high-intensity outbreak followed by amphibian population stabilisation and pathogen persistence at lower levels.

全球两栖动物的减少速度超过了地球上大多数生物的消失速度。由水蛭壶菌(Batrachochytrium dendroatidis, Bd)引起的泛动物真菌疾病壶菌病被广泛认为是两栖动物生物多样性侵蚀的主要驱动因素。然而,在全球范围内对生物多样性与灭绝风险之间关系的综合分析仍然缺乏。利用全球Bd检测数据库和IUCN灭绝风险红色名录,我们发现目前两栖动物的减少只与温带地区的Bd有关,而历史分析显示,1980-2004年期间,更多赤道地区的Bd相关下降达到了过去的峰值,但在最近几十年(2004-2020年),这种下降的强度有所减弱。相比之下,温带物种在1980-2004年期间没有出现与bd相关的下降,但目前正在显著下降。我们认为,温带地区较短的活动季节可能起到了“自然封锁”的作用,延迟了Bd对易感物种的湮灭作用。相反,在两栖动物更密集的赤道地区,全年的活动可能触发了向动物流行病后动态的更快过渡,其特征是持续的高强度暴发,随后是两栖动物种群稳定和病原体在较低水平上的持久性。
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Global Change Biology
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