Abstract
This literature review synthesizes the role of soil moisture in regulating carbon sequestration and greenhouse gas emissions (CS-GHG). Soil moisture directly affects photosynthesis, respiration, microbial activity, and soil organic matter dynamics, with optimal levels enhancing carbon storage while extremes, such as drought and flooding, disrupt these processes. A quantitative analysis is provided on the effects of soil moisture on CS-GHG across various ecosystems and climatic conditions, highlighting a “Peak and Decline” pattern for CO₂ emissions at 40% water-filled pore space (WFPS), while CH₄ and N₂O emissions peak at higher levels (60–80% and around 80% WFPS, respectively). The review also examines ecosystem models, discussing how soil moisture dynamics are incorporated to simulate photosynthesis, microbial activity, and nutrient cycling. Sustainable soil moisture management practices, including conservation agriculture, agroforestry, and optimized water management, prove effective in enhancing carbon sequestration and mitigating GHG emissions by maintaining ideal soil moisture levels. The review further emphasizes the importance of advancing multiscale observations and feedback modeling through high-resolution remote sensing and ground-based data integration, as well as hybrid modeling frameworks. The interactive model-experiment framework emerges as a promising approach for linking experimental data with model refinement, enabling continuous improvement of CS-GHG predictions. From a policy perspective, shifting focus from short-term agricultural productivity to long-term carbon sequestration is crucial. Achieving this shift will require financial incentives, robust monitoring systems, and collaboration among stakeholders to ensure sustainable practices effectively contribute to climate mitigation goals.
Similar content being viewed by others
Introduction
Ecosystem carbon sequestration and greenhouse gas emissions (CS-GHG) are complex and crucial aspects of climate change mitigation. These primarily involve two interconnected processes: carbon sequestration and the dynamic interplay in the emissions of nitrous oxide (N2O) and methane (CH4)1,2. Carbon sequestration, known for its cost-efficiency and natural approach, not only addresses global warming3 but also improves soil fertility4, enhances water retention5, and increases agricultural productivity6,7. While carbon sequestration effectively reduces atmospheric CO2 levels through storage in land-based ecosystems such as forests, grasslands, wetlands, and agricultural lands8,9,10, it can inadvertently lead to increased emissions of N2O and CH4, gases with higher global warming potentials than CO211,12. For example, the application of nitrogen fertilizers in afforestation projects can enhance soil carbon storage but also stimulate nitrification and denitrification processes that release N2O13. Similarly, efforts to enhance carbon sequestration by wetlands can lead to waterlogged conditions, creating anaerobic environments ideal for methanogenesis, thus increasing CH4 emissions14. Recognizing carbon sequestration's effectiveness in reducing CO2 levels and its potential impact on GHG dynamics, the Intergovernmental Panel on Climate Change (IPCC) acknowledges the importance of carbon sequestration in soils and the relevance of managing N2O and CH4 emissions as integral components of climate change mitigation strategies15.
Various factors influence CS-GHG, including soil and vegetation types, climate factors, and human management practices such as irrigation and fertilization16,17,18. Among these factors, the amount of water available in soil impacts plant growth, microbial activity, and soil organic matter, all of which play crucial roles in determining the rate and efficiency of CS-GHG19,20,21. Model-based studies have also found that the variability in global modeled land carbon uptake is chiefly driven by the effects of temperature and vapor pressure deficit, both of which are modulated by soil moisture22. The impact of soil moisture on CS-GHG is more often analyzed as a part of multiple environmental variables than stand-alone, and most experimental data are derived from site-specific studies, lacking comprehensive analysis. There is also a significant need to understand how extreme weather events like droughts and flooding impact CS-GHG dynamics in different regions and to better understand soil moisture thresholds for CS-GHG. Additionally, it is crucial to evaluate how various models simulate the effects of soil moisture on CS-GHG to improve prediction accuracy and guide future research.
The primary objective of this literature review is to synthesize the current state of knowledge on the interactions between soil moisture and CS-GHG. This review seeks to elucidate the intricate relationships between soil moisture, microbial activity, plant physiology, and soil organic matter dynamics, as well as to identify the critical thresholds and mechanisms that govern these processes across diverse ecosystems. To achieve this goal, the review aims to: 1) provide an overview of key mechanisms involved in CS-GHG and examine the impacts of soil moisture on these processes; 2) explore the patterns of CO2, CH4, and N2O emissions in response to soil moisture variations, identifying the specific conditions that lead to peak emissions and the implications for climate change mitigation; 3) explore how sustainable soil moisture-related land management practices can enhance carbon sequestration and reduce GHG emissions, emphasizing the implementation of techniques like conservation agriculture, agroforestry, and optimized water management, and 4) highlight the importance of integrating soil moisture considerations into climate mitigation policies and outline future research directions to address knowledge gaps and improve the modeling of soil moisture-carbon dynamics. By reviewing the literature on soil moisture and CS-GHG interactions, this review aims to provide valuable insights for researchers, practitioners, and policymakers working to develop effective strategies for enhancing terrestrial carbon storage and mitigating climate change.
Mechanisms of soil moisture influence on carbon sequestration and greenhouse gas emissions
Soil moisture influences CS-GHG through three key mechanisms (Fig. 1): plant photosynthesis and respiration, soil microbial activity, and soil organic matter decomposition and stabilization. These mechanisms are not isolated but are interdependent, each influencing and being influenced by the others23. Soil moisture, for instance, affects plant health and photosynthesis rates, which in turn impact soil microbial communities through root exudates and litter inputs24. Microbial activity influences the decomposition of organic matter, altering soil structure and nutrient availability, which feedback into plant growth and soil moisture dynamics25.
In the right yellow box, white arrows represent soil moisture, yellow arrows indicate CO2 absorption during photosynthesis, red arrows denote CO2 release during autotrophic respiration, and blue arrows show water transport from soil to plants through plant hydraulics. The left green box includes light green arrows for N2O and CH4 release under anaerobic conditions, and dark green arrows for methane oxidation and nitrification to N2O under aerobic conditions. The middle purple box features purple arrows illustrating CO2 production through decomposition and stabilization. The diagram illustrates how soil moisture participates in various CS-GHG processes, indicating interrelated feedback mechanisms within terrestrial ecosystems.
Plant photosynthesis and respiration
Soil moisture is a critical factor in regulating photosynthesis, and insufficient soil moisture has been observed to limit plant photosynthesis globally26. Variability in soil moisture accounts for approximately 90% of the inter-annual variability in global land carbon uptake, mainly through its influence on plant carbon assimilation22. In dryland regions like central Asia, soil moisture promotes photosynthesis in up to 94% of vegetation areas, with its effects surpassing those of vapor pressure deficit in 74% of these areas, especially in croplands, grasslands, and forests27. Globally, soil moisture constraints are estimated to reduce annual photosynthesis by around 15% and intensify interannual variability by over 100% across 25% of vegetated land28. Increased precipitation in desert steppes has been shown to enhance net photosynthetic rates by 159.5% and 178.9% for C3 and C4 plants, respectively, underscoring soil moisture’s role in promoting photosynthetic activity29.
Soil moisture influences respiration in both plants and soil organisms, affecting autotrophic respiration (Ra) and heterotrophic respiration (Rh) differently. Studies show that Ra, which includes respiration from all plant tissues (roots, stems, and leaves) and associated organisms, is generally more sensitive to soil moisture fluctuations than Rh, which is driven by microbial decomposition of organic matter. For example, drought reduced Ra contributions to total soil respiration from 33% to 16% in a subtropical forest30 and from 66% to 35% in dry grasslands31, highlighting Ra’s sensitivity to water limitations. In contrast, Rh remained relatively stable, decreasing by only 21% under drought compared to a 26.8% reduction in Ra32. Moisture thresholds further underscore this sensitivity in Mediterranean forests, Ra decouples from temperature below a 17% soil moisture threshold, while Rh is moisture-controlled below 20%33. Moisture pulses also reveal differential responses, with Rh increasing over sixfold within hours of rainfall, while Ra takes days to respond33.
Adding to the complexity, the inclusion of plant hydraulics into our understanding of carbon sequestration mechanisms provides a critical dimension34. Plant hydraulics, the system plants use to transport water from the soil through their roots and stems to the leaves, is integral to photosynthesis and overall plant health35. Adequate soil moisture ensures that plants have sufficient water to maintain this transport, which is essential for optimal photosynthetic performance36. When plants efficiently photosynthesize, they absorb more CO2 and convert it into organic carbon, thus contributing to carbon sequestration. Conversely, under conditions of water stress, hydraulic failure can occur, reducing photosynthetic efficiency and consequently carbon assimilation.
Soil microbial activity
Soil moisture critically influences soil microbial activity by affecting the habitat conditions of microorganisms such as bacteria, fungi, and archaea37. Microbial processes are enhanced at optimal moisture levels, with studies showing that microbial activity at 100% water holding capacity (WHC) can be up to 41% higher than at 60% WHC38. Soil moisture impacts not only the overall activity but also the enzyme activities, distribution, and function of specific microbial groups39. It determines the balance between aerobic and anaerobic conditions, thereby influencing which microorganisms dominate40.
The influence of soil moisture on microbial activity directly affects carbon sequestration. Microorganisms decompose organic matter and convert it into stable soil carbon forms through enzymatic reactions37. Under optimal, moist, and aerobic conditions, microbes efficiently break down organic matter, with a portion being stabilized through association with soil minerals, contributing to long-term carbon storage. Fungi, for example, assimilate carbon into their hyphae, and their growth is significantly influenced by soil moisture levels41. Additionally, microbial autotrophy including autotrophic bacteria and phototrophic protists fixes atmospheric CO₂ into soil carbon42. Soils with optimal moisture, such as paddy soils, support a higher proportion of these organisms, resulting in higher CO₂ fixation rates compared to drier upland and forest soils43.
Soil moisture also impacts GHG emissions by influencing the metabolic pathways of soil microorganisms. In well-aerated soils with optimal moisture, aerobic microbial activity predominates, leading primarily to CO₂ production44. However, in waterlogged or anaerobic soils, microbial pathways shift toward anaerobic processes. Denitrifying bacteria become more active under these conditions, producing increased levels of N₂O, while methanogenic archaea generate CH₄45. Soil moisture affects the activity of methanotrophic bacteria that oxidize CH₄ into CO₂, mitigating methane emissions. This activity is especially crucial in environments like wetlands and rice paddies, where methane production is prevalent46,47.
Soil organic matter decomposition and stabilization
Building upon the role of soil microbial activity discussed in Section 2.2, soil moisture further influences CS-GHG through its impact on soil organic matter (SOM) decomposition and stabilization. Adequate moisture enhances microbial metabolism and enzyme activity, leading to increased breakdown of organic matter. For instance, CO₂ production can be 31–40% higher at 65% WHC compared to 45% WHC, indicating that moisture availability significantly affects SOM mineralization rates48. Soil moisture also influences carbon stabilization by promoting the formation of mineral-associated organic matter; in wetter climates, greater root growth and interaction of organic inputs with soil minerals enhance carbon stabilization49.
The balance between SOM decomposition and stabilization is crucial for carbon sequestration. While decomposition releases CO₂, the stabilization of organic matter within soil aggregates or bound to minerals contributes to long-term carbon storage. Soil moisture facilitates the formation of stable soil aggregates through the swelling of clay minerals and cohesion of soil particles, encapsulating organic matter and protecting it from further decomposition50,51. Changes in moisture regimes can significantly impact carbon stabilization in soils, with a tipping point observed where precipitation equals evaporation49.
SOM decomposition and stabilization processes influenced by soil moisture have significant implications for GHG emissions. Increased decomposition rates under optimal moisture conditions lead to higher CO₂ emissions due to enhanced microbial respiration. Excessive moisture can create anaerobic conditions, shifting microbial activity towards methanogenesis and resulting in increased CH₄ production52. Soil aggregates significantly influence GHG dynamics, particularly CH4 and N2O emissions, by modulating soil gas diffusion and water availability53,54.
The interplay of soil moisture and other key factors regulating CS-GHG dynamics
Soil moisture interacts with various other soil properties—such as temperature, texture, type, pH, carbon-to-nitrogen (C/N) ratio, bulk density, and nitrogen input—to regulate the complex dynamics of CS-GHG. Soil temperature, in particular, has a profound influence on microbial activity and organic matter decomposition, both of which drive CO₂ and N₂O fluxes55,56. In well-moistened soils, higher temperatures can accelerate microbial decomposition, leading to increased carbon mineralization and subsequent carbon losses57. However, in dry soils, microbial activity may decrease despite elevated temperatures. For example, soil microbial respiration in global drylands often adapts to the ambient thermal regime, reducing the expected increase in CO₂ emissions58,59. These findings suggest that temperature-driven increases in soil respiration are modulated by other factors, with soil moisture playing a critical role in shaping how microbial communities respond to warming. Soil texture also governs the interaction between temperature and moisture, as coarse-textured soils (e.g., sandy soils) typically exhibit faster drainage, which limits the water availability for microbial processes60. In contrast, fine-textured soils (e.g., clay soils) retain moisture, allowing temperature and moisture to co-regulate carbon cycling processes more effectively60. Additionally, the C/N ratio and nitrogen input are critical factors that shape microbial nutrient availability and nitrogen cycling, significantly impacting N₂O emissions61. In organic soils from mid-latitude regions, N₂O emissions follow a Gaussian distribution with respect to the C/N ratio, peaking at values around 18–1962. Research has shown that the C/N ratio alone can explain up to 36% of the variability in N₂O fluxes. However, when other factors—such as mineral nitrogen input and water table depth—are considered, the explanatory power increases to 75%63. To further the complexity, soil pH has been used as an integrated proxy of land use change, parent material and climate to determine the site-specific effects of land management strategies on soil organic accumulation, thus CS-GHG64. The combination of these factors—temperature, moisture, soil texture, pH, and nutrient availability—collectively influences CS-GHG dynamics. Among them, soil moisture, as one of the most rapidly changing and sensitive factors65, becomes the pivotal element in determining the overall outcome of CS-GHG emissions66.
Quantitative impact of soil moisture variability on carbon sequestration and greenhouse gas emissions
Influence of soil moisture on carbon sequestration
Table 1 presents the impact of soil moisture on carbon sequestration across various global locations and ecosystems. Generally, there are three distinct scenarios: lower soil moisture reducing carbon sequestration, higher soil moisture enhancing carbon sequestration, and higher soil moisture reducing carbon sequestration.
Lower soil moisture often results from drought conditions, which significantly impact carbon sequestration. On a global scale, data from four Earth system models indicate that drying soil moisture trends reduce the current land carbon sink by about 2–3 Gt C per year67. This effect is particularly pronounced in arid regions, where drought conditions limit the carbon sequestration potential68,69. For instance, in Sudan’s sparse savanna, rainy season carbon uptake averages 152 mmol CO₂ m−2 day−1, while dry season uptake drops to just 14.7 mmol CO₂ m−2 day−1, a nearly tenfold difference that significantly reduces the region’s annual carbon sink capacity. Similarly, in the cold Pan-Arctic area, decreased soil moisture during summer limits peak plant productivity, with gross primary production (GPP) declining by up to 27% as soil moisture decreases from 60% to 31%70. In moisture-rich ecosystems like the Amazon rainforest, drought can severely impact carbon sequestration, causing significant tree mortality, reduced carbon uptake, and leading to a net biomass carbon loss of 1.2 to 1.6 Pg out of the 18 Pg it processes annually71. In China’s humid and warm eastern regions72, national and regional net ecosystem productivity anomalies were closely correlated with drought index, highlighting the drought impact on carbon dynamics. In subtropical forests73, drought led to soil carbon storage declines of up to 12.2%, reflecting significant reductions in carbon sequestration under moisture stress.
In some regions, inherently high soil moisture leads to enhanced carbon sequestration. For instance, in peatlands and wetlands, high soil moisture content creates low-oxygen conditions that slow down decomposition, resulting in effective carbon storage74. Although carbon storage is expected to decline under warming and drying in boreal peatlands75, declining soil moisture alone does not seem to necessarily cause reduced carbon storage76. In semi-arid regions like Australia, significant carbon sink activity has been observed following heavy rainfall, with an increase in annual rainfall of about 350 mm leading to an additional carbon absorption of approximately 0.4 ± 0.2 Pg C by Australia's terrestrial ecosystems77. Similarly, higher soil moisture in areas like the Qinghai-Tibetan Plateau, Xinjiang, and Northwest China has been shown to promote carbon sink activity, contributing to net ecosystem productivity increases of up to 3.0 g C m² per year78.
However, high soil moisture can also reduce carbon sequestration under certain conditions. In ecosystems that have experienced prolonged dry periods, a sudden increase in soil moisture due to rainfall can lead to rapid carbon loss79. This occurs because the added moisture reactivates previously dormant microorganisms in the soil, causing them to release CO₂ as they metabolize organic material80. Additionally, increased moisture enhances the diffusion of organic matter, which, in combination with higher microbial activity, contributes to a spike in CO₂ emissions80. Additionally, elevated CO2 concentrations can exacerbate this effect81. High CO2 levels typically promote plant growth, leading to more extensive root systems82. Under high moisture conditions, increased root respiration generates more CO2, thereby reducing net carbon sequestration83,84.
Hot spots and hot moments in soil moisture thresholds for GHG emissions
Table 2 provides a detailed analysis of the correlation between soil moisture (measured as water-filled pore space, WFPS) and GHG emissions across diverse locations and landcover types. The correlation patterns for CO2 are consistently described as "Peak and Decline" (PD), indicating that CO2 emissions tend to reach a peak at a specific soil moisture level before declining. In contrast, CH4 and N2O correlations exhibit more variability, with patterns described as "Positive" (P), "Peak and Decline" (PD), and "Trough and Rise" (TR). Table 2 also identifies the WFPS thresholds at which peak emissions occur, revealing that CO2 emissions typically peak at around 40% WFPS. Meanwhile, CH4 and N2O emissions generally peak at higher soil moisture levels, with CH4 peaking between 60% and 80% WFPS and N2O peaking at approximately 80% WFPS. The consistent "Peak and Decline" pattern observed for CO2 emissions across various landcovers suggests that there is an optimal soil moisture level for microbial activity and root respiration, beyond which emissions decline due to either excess moisture limiting oxygen availability or insufficient moisture restricting microbial processes. This optimal level is typically around 40% WFPS, indicating a critical threshold for CO2 emissions regulation. For instance, in European landcover categories21, CO2 emissions peak at around 40% WFPS before declining. In contrast, CH4 and N2O emissions show significant variability in response to soil moisture. CH4 emissions tend to peak at higher soil moisture levels, ranging from 60% to 80% WFPS, which aligns with the anaerobic conditions favorable for methane production85. For example, CH4 emissions in European wetlands peak at 95% WFPS21, and in Chinese paddy fields, they peak at 99% WFPS86. Similarly, N2O emissions peak at even higher moisture levels, around 80% WFPS, reflecting the conditions that promote denitrification processes. This is evident in the European forest landcover category, where N2O emissions peak at around 80% WFPS21. Other landcover types also exhibit similar trends. For example, in UK croplands, N2O emissions peak at around 75% WFPS83. In Danish forests, N2O emissions peak at 60% WFPS, while CH4 emissions show a positive correlation at 80% soil water content87. For grasslands experiencing freeze-thaw cycles in China, CO2 and N2O emissions both peak at around 50% WFPS88.
The observed variability in CH4 and N2O emission patterns underscores the complex interactions between soil moisture and microbial processes responsible for GHG production. While CO2 emissions demonstrate a more predictable response to soil moisture changes, CH4 and N2O emissions are influenced by a broader range of soil moisture conditions, highlighting the need for targeted soil moisture management strategies to mitigate these emissions. Overall, managing soil moisture to maintain optimal conditions for microbial activity can significantly impact the regulation of GHG emissions and contribute to climate change mitigation efforts.
The impact of free-thaw and drought-rewetting events on GHG emissions
Freeze-thaw cycles (FTCs) and drought-rewetting events cause abrupt shifts in soil physical, chemical, and biological processes, significantly altering GHG emissions. FTCs can increase GHG emissions by disrupting soil aggregates, releasing dissolved organic carbon, and causing microbial cell rupture, which releases carbon and nitrogen89. This process can cause CO₂ emissions to account for about 45% of annual totals and N₂O emissions to originate 50–70% from these cycles, with emissions increasing by up to 1.7 times for CO₂ and up to 5.8 times for N₂O90, especially in agricultural soils where perennial bioenergy crops such as miscanthus and willow are grown, due to accelerated nitrogen losses91. Ecosystems respond variably to FTCs, for example, in wetland ecosystems, flooding during FTCs may reduce CO₂ emissions by 65% and CH₄ emissions by 37%92. Alpine forests tend to show increased CO₂ emissions during thawing93, primarily because soil respiration during FTCs averages a fourfold increase compared to non-FTCs. In temperate grasslands, FTCs have varying impacts on GHG emissions depending on soil properties and land cover: meadow steppe, marshland, and typical steppe soils exhibit increased N₂O emissions, whereas arid steppe soils show minimal response94. While FTCs primarily disrupt soil structure and enhance microbial activity, rewetting events trigger rapid shifts in soil moisture, which similarly affect the carbon and nitrogen cycling. During droughts, microbial activity slows, leading to temporary carbon accumulation95. However, rewetting triggers a sharp increase in microbial respiration, resulting in large CO₂ emission bursts as accumulated organic matter is rapidly decomposed96,97. A meta-analysis of global drying and rewetting cycles across all ecosystems showed that these cycles increase CO₂ emissions by 35.7% compared to constant soil moisture conditions, while having no significant effect on N₂O emissions98. In contrast, when wetlands are rewetted and the water table rises near the surface (within –30 cm to –5 cm of the surface), GHG emissions are often reduced to near zero due to waterlogged conditions slowing down microbial activity99.
In summary, freeze-thaw cycles and drought-rewetting events typically increase CO₂ and N₂O emissions by disrupting soil structure and enhancing microbial activity, especially in agricultural soils. Rewetting triggers a surge in CO₂ emissions as accumulated organic matter is rapidly decomposed. However, in wetlands, rising water tables tend to reduce GHG emissions by slowing down microbial activity.
Carbon sequestration and greenhouse gas emission models in the context of soil moisture dynamics
Ecosystem models offer detailed simulations of ecosystem processes, making them valuable for understanding the intricate dynamics of carbon, nutrient, energy, and water cycles100,101,102,103,104,105,106,107,108,109. Table 3 provides a detailed comparison of how various state-of-science ecosystem models incorporate soil moisture's influence on the CS-GHG.
In carbon sequestration, different ecosystem models incorporate soil moisture’s role in CS with varying emphasis on specific mechanisms. For example, the Common Land Model (CoLM) focuses on stomatal conductance, a vital process for photosynthesis, where water availability regulates the opening and closing of plant stomata, directly impacting carbon uptake by vegetation109. Similarly, Biome-BGC emphasizes drought stress levels, which impact net primary productivity by influencing plant growth and carbon storage potential, especially under changing water conditions100. Other models, such as Organizing Carbon and Hydrology in Dynamic Ecosystems (ORCHIDEE)103 and Lund-Potsdam-Jena General Ecosystem Simulator (LPJ-GUESS)104, go further by embedding water stress into carbon allocation processes, thereby affecting carbon dynamics within the ecosystem. Denitrification-Decomposition (DNDC)101 and Dynamic Land Ecosystem Model (DLEM)107,108 add layers of complexity by linking soil moisture to microbial activity and nutrient cycling, which are critical for long-term carbon storage in soils.
When addressing GHG emissions, models differ in the extent and processes simulated. Models such as Biome-BGC100 and BEPS-TerrainLab V2.0110 only simulate CO₂ emissions. In contrast, models like DLEM, DNDC, Community Land Model Version 5 (CLM5), and Land Model of U.S. Department of Energy Energy Exascale Earth System Model (ELM) can also simulate CH₄ and N₂O emissions. Additionally, some models have expanded CH₄ simulation capabilities by integrating peatland schemes, such as ORCHIDEE-PEAT111 and LPJ-GUESS version 4.1112.
For CO₂, models such as Biome-BGC and BEPS-TerrainLab V2.0 represent the role of soil moisture in GHG emissions indirectly, focusing primarily on plant-mediated CO₂ fluxes. In contrast, models like CoLM, DLEM, CLM5 and ELM take a more comprehensive approach by simulating CO₂ release not only from plant photosynthesis, soil respiration, and microbial decomposition but also by incorporating fire susceptibility influenced by soil moisture, where low moisture levels increase fire risk and subsequently CO₂ emissions108,111,112,117,118. For CH4 and N2O, DLEM links soil moisture to CH₄ emissions by modeling anaerobic methanogenesis under wet conditions and CH₄ oxidation in drier soils107,108. DNDC builds on this approach by tracking daily soil moisture levels, which directly affect microbial respiration and redox conditions essential for N₂O and N₂ emissions, using the “anaerobic balloon” concept101. CLM5 and ELM capture additional complexities by modeling the anaerobic processes necessary for CH₄ and N₂O production, especially in wetlands where high soil moisture creates conducive environments for methanogenesis106.
In sum, soil moisture serves as a key regulator in balancing CS and CO₂ emissions, indirectly influencing ecosystem carbon dynamics through its effects on plant growth, stomatal conductance, and microbial decomposition. However, when it comes to CH₄ and N₂O, soil moisture plays a direct role, actively controlling emissions by influencing the soil’s redox environment and microbial activity. In anaerobic conditions, especially in wetlands or saturated soils, soil moisture promotes methanogenesis, leading to CH₄ emissions, while also driving N₂O production through nitrification and denitrification processes.
Sustainable soil moisture-related land management practices
Enhancing carbon sequestration
Conservation Agriculture (CA) is a recommended sustainable land management practice for enhancing carbon sequestration113. CA involves leaving crop stubble/leaf litters on the soil surface to preserve soil moisture, reduce erosion, and improve soil structure113. By incorporating legumes into the cropping system, CA helps sequester carbon by protecting soil organic carbon in aggregates and adding organic carbon to deeper soil layers114. Additionally, CA practices not only increase soil productivity and crop yields but also contribute to reverting soil degradation and improving input use efficiency. Therefore, promoting ___location-specific CA practices is crucial for sustainable soil management and enhancing carbon sequestration. Cover cropping and mulching, as part of CA practices, are essential sustainable soil moisture-related land management practices that play a crucial role in enhancing carbon sequestration115. Cover cropping helps to improve soil health by increasing organic matter content, which in turn enhances soil carbon sequestration potential116. Mulching, on the other hand, aids in reducing soil erosion, maintaining soil moisture levels, and promoting the decomposition of organic matter, all of which contribute to increased carbon sequestration in the soil117. These practices, along with other techniques like conservation tillage, nutrient management, and crop residue management, are vital for maximizing carbon sequestration in terrestrial ecosystems, mitigating greenhouse gas emissions, and promoting sustainable agriculture118.
Agroforestry practices play a crucial role in sustainable soil moisture-related land management for enhancing carbon sequestration119. These practices involve the integration of trees and shrubs into agricultural landscapes, promoting soil health and carbon storage120. Agroforestry systems contribute to carbon sequestration by increasing organic matter inputs to the soil, enhancing soil structure, and reducing erosion119,120. By combining agriculture with forestry, agroforestry helps maintain soil moisture levels, which are essential for promoting plant growth and carbon sequestration121. Additionally, agroforestry practices offer multiple benefits such as improved biodiversity, increased resilience to climate change, and sustainable land use. Therefore, implementing agroforestry techniques can be a valuable strategy for enhancing carbon sequestration while promoting sustainable soil moisture-related land management.
The application of organic amendments, such as compost and manure, can improve soil moisture retention and increase carbon sequestration by enhancing soil structure, organic matter content, and WHC122. Aerosols, such as mineral dust and black carbon, can influence soil moisture and carbon sequestration by affecting the Earth's radiation balance and altering precipitation patterns123. For instance, mineral dust aerosols can have a cooling effect on the Earth's surface, potentially reducing evapotranspiration and altering soil moisture dynamics124. Black carbon aerosols, on the other hand, can have a warming effect, potentially increasing evapotranspiration and reducing soil moisture125.
Reducing GHG emission
Sustainable soil moisture-related land management practices are essential for reducing GHG emissions, particularly in agricultural systems like rice paddies, which are significant sources of CH4. One effective practice is improved water management in rice systems, such as alternate wetting and drying (AWD)126. AWD involves periodically draining the rice fields rather than keeping them continuously flooded. This practice reduces CH4 emissions by limiting the anaerobic conditions that favor methanogenic bacteria responsible for methane production. Studies have shown that AWD can cut CH4 emissions by up to 50% compared to traditional continuous flooding methods127. In addition to AWD, other sustainable practices include optimizing irrigation scheduling to match crop water needs more precisely, thereby avoiding excessive water application that leads to anaerobic soil conditions128. Implementing water-saving technologies such as drip irrigation or controlled flooding can further enhance water use efficiency and reduce GHG emissions129. Moreover, incorporating organic amendments like biochar into the soil can improve soil structure, increase water retention, and reduce N2O emissions by promoting more efficient nutrient cycling and reducing the need for synthetic fertilizers130. Collectively, these practices not only mitigate GHG emissions but also improve water use efficiency, enhance soil health, and boost crop productivity. Sustainable water management in rice systems exemplifies how targeted land management practices can address both environmental and agricultural challenges, contributing to more resilient and climate-smart agricultural systems.
Challenges and future directions
Enhancing CS-GHG monitoring with high-resolution remote sensing and ground-based observations
High-resolution data on water and carbon are crucial for CS-GHG. Synthetic Aperture Radar (SAR) has demonstrated sensitivity to surface soil moisture131, and when combined with LiDAR, it has become a promising alternative to traditional field data campaigns132. For soil moisture, SAR platforms like Sentinel-1 and -2, utilizing multi-orbit time series analysis and incidence angle normalization, and combining various downscaling algorithms, achieve spatial resolutions enabling precise monitoring of soil moisture at scales of 1 km133, 500 m134, and even 100 m135. LiDAR-derived digital elevation models, combined with machine learning, enable the production of high-resolution soil moisture products down to 2 m136. In specific terrains, such as coastal area, combining LiDAR intensity data with machine learning can achieve spatial resolutions at the centimeter to decimeter scale137. For carbon, LiDAR missions such as GEDI and ICESat-2 deliver detailed forest canopy height data138, allowing ecosystem models to dramatically improve the spatial resolution of carbon flux estimates—from 0.25° to 0.01°139. This enhanced resolution captures fine-scale forest structures and disturbances, which are crucial for precise CS-GHG analysis and modeling. However, these high-resolution datasets often rely on machine learning, which is constrained by the availability and quality of training data133,135,136. In soil moisture mapping, while SAR provides frequent temporal updates, its accuracy declines in areas with dense vegetation140. Similarly, LiDAR’s detailed spatial resolution is offset by limited temporal coverage, making it challenging to capture fast-changing soil moisture dynamics effectively141. In carbon flux modeling, although LiDAR excels at capturing canopy height and overall forest structure, representing critical below-canopy processes for carbon flux remains difficult, further adding to the complexity of accurate modeling139.
To address these limitations and fill the gaps in remote sensing, site-level to watershed-scale observations provide high-quality, continuous measurements of soil moisture, carbon fluxes, and GHG emissions, which are essential for validating and complementing remote sensing data. FLUXNET is a global network of eddy covariance towers that measure exchanges of carbon dioxide, water vapor, and energy between terrestrial ecosystems and the atmosphere142. This network offers detailed insights into ecosystem responses to environmental changes across diverse biomes143. The DOE Next-Generation Ecosystem Experiments Arctic (NGEE-Arctic; https://ess.science.energy.gov/ngee-arctic/) and NGEE-Tropics (https://ess.science.energy.gov/ngee-tropics/) programs focus on improving the representation of Arctic and tropical ecosystems in Earth system models by collecting extensive field observations on plant physiology, soil properties, and biogeochemical processes under changing environmental conditions144,145. Additionally, the Spruce and Peatland Responses Under Changing Environments (SPRUCE; https://mnspruce.ornl.gov/) experiment investigates the effects of elevated temperature and carbon dioxide levels on peatland ecosystems. These researches provide critical insights into the complex interactions and feedback loops between soil water availability, carbon sequestration, and GHG emissions under shifting environmental conditions146. Emphasizing these smaller-scale observations underscores their essential role in validating and complementing remote-sensing data, enhancing our understanding and modeling of soil moisture and CS-GHG dynamics across diverse ecosystems. However, significant challenges remain. Spatial and temporal mismatches between site-level measurements and remote sensing complicate data integration due to differences in scale, protocols, and data quality147. Additionally, inconsistencies in instrumentation and methodologies across studies introduce variability, further complicating data synthesis and model validation processes148.
Future research should prioritize enhancing multiscale observational capabilities by integrating high-resolution remote sensing data with ground-based networks. Specifically, this involves expanding the geographical coverage of observational sites to improve data representation in underrepresented and remote regions149,150. Developing below-ground sensors to strengthen ground-based observations of below-canopy processes will enhance our understanding of ecosystem dynamics150,151. By combining these enriched ground observations with remote sensing results and employing data fusion techniques, we can create high-quality datasets with high spatial and temporal resolution. This comprehensive approach will address limitations in densely vegetated areas and regions with limited temporal coverage, ultimately leading to more accurate modeling and analysis of soil moisture and carbon-greenhouse gas dynamics across various ecosystems.
Bridging the gaps in modeling soil moisture and CS-GHG dynamics interaction: challenges and opportunities
Aside from the challenges associated with data, accurately modeling interactions between soil moisture and CS-GHG remains a significant challenge. First, carbon dynamics are highly sensitive to water availability152, and the processes involved are complex153. As discussed in Section 3.2, CH₄ and N₂O emissions are influenced by a broader range of soil moisture conditions. Modeling these nonlinear and threshold-based responses is challenging. Second, soil moisture exhibits significant spatial and temporal variability. Spatially, it varies across different landscapes due to factors like soil type, topography, climate, and vegetation cover154. Temporally, soil moisture can change rapidly due to weather events like rainfall or droughts155. This rapid and complex spatiotemporal variability makes it challenging for models, which must balance computational efficiency with the need for detailed process representation. Third, complex plant-soil interactions pose significant modeling challenges. Different plant species and microbial communities respond uniquely to soil moisture changes156. These interactions are complex; while small-scale model experiments can capture some aspects, large-scale models require detailed classification of plant functional types and microbial community compositions to accurately represent these dynamics and their impact on ecosystems.
As reviewed in Section 4, current ecosystem models can capture the complex feedback between soil moisture and CS-GHG to varying degrees. However, expanding the representation of these feedback from offline ecosystem models to an Earth system modeling framework presents additional challenges. These challenges include achieving accurate representation of temporal and spatial variability, realistically representing the interactions between soil moisture dynamics and atmospheric processes within a fully coupled, real-time framework, and efficiently managing computational demands157. Additional complexities arise in representing the legacy effects of droughts, which can alter soil properties by changing its chemical and physical structure, reducing carbon sequestration (Table 1) and increasing greenhouse gas emissions158,159,160. Accurately modeling plant hydraulic responses and capturing the often-underestimated strength of land–atmosphere interactions are also essential, as they directly influence the simulation of energy, moisture, and carbon exchanges161. Moreover, the influence of human activities, such as irrigation, water extraction, and those human land management practices discussed in Section 5, which significantly affect CS-GHG processes and their climate feedback, is often underrepresented in ecosystem models and their parent Earth system models (ESMs)162,163,164.
To address these modeling challenges, recent studies have increasingly advocated for incorporating key ecological processes into ecosystem models and associated ESMs to enhance process-based representations and the accuracy and relevance of these models165,166. Integrating advanced machine learning algorithms is another promising approach. At the forefront of this integration are hybrid modeling frameworks, which combine and integrate machine learning methods into classical process-based models167. For example, the Knowledge-Guided Machine Learning (KGML) framework combines process-based models with machine learning techniques to improve carbon cycle quantification, revealing 86% more spatial detail than conventional methods168. Similarly, the KGML-DA framework improves carbon cycle predictions, reducing RMSE by up to 30.5% for corn and 24.6% for soybean, across three agricultural sites and 627 counties in the U.S. Midwest, using data from 2000 to 2020169. Hybrid models that integrate machine learning into ESMs combine the predictive power of machine learning with the interpretability of process-based models for improved accuracy170. Recent advancements, such as Bayesian networks and data assimilation techniques, enable these models to dynamically update predictions with new data and manage uncertainty effectively171.
Beyond challenges inherent in the models themselves, obstacles arise in integrating models with observational data due to differences in spatiotemporal coverage, such as models providing high-frequency carbon flux outputs while MODIS GPP is available only every 16 days. Additional challenges include variations in data scale, resolution, and inconsistencies in data formats and quality148. Moreover, uncertainties in observational data can impact the validation and calibration processes, leading to less reliable predictions172. The Department of Energy's iterative Model-Experiment (ModEx; https://ess.science.energy.gov/modex/) approach offers a valuable framework for bridging the gaps between observation and modeling. This iterative process emphasizes a synergistic cycle where observational and experimental data inform and refine models, while models guide and prioritize future data collection efforts. By applying the ModEx concept to integrate high-resolution remote sensing data with expanded ground-based observations (as discussed in Section 6.1), researchers can enhance the predictive capabilities of models related to soil moisture and CS-GHG dynamics. This continuous feedback loop enables the identification of critical variables, processes, and locations that warrant further investigation, thereby enhancing the efficiency of data acquisition and informing targeted model development159,160,161,162,163.
Policies and incentives for soil moisture management to enhance CS and reduce GHG emissions
Current policies and incentives aimed at optimizing soil moisture for CS and reducing GHG emissions face several key challenges. One major issue is the misalignment between land use policies and climate goals, particularly in the agricultural and forestry sectors173. Many existing programs prioritize short-term outcomes like crop yield improvements, often at the expense of long-term soil health and carbon sequestration benefits174,175. This narrow focus on immediate agricultural outputs undermines efforts to manage soil moisture effectively for climate mitigation176,177. Furthermore, certain management practices that improve carbon sequestration, like afforestation or conservation tillage, may inadvertently increase GHG emissions, highlighting the need for policies that address these trade-offs effectively44,178. Financial incentives, such as subsidies and payments for ecosystem services (PES), can encourage the adoption of sustainable land management practices that improve soil health and increase carbon storage179. Programs like the USDA's Environmental Quality Incentives Program (EQIP) provide financial and technical assistance to help implement long-term conservation practices that enhance soil, water, and air quality180. Economic mechanisms, such as carbon credits and emissions trading, can encourage land use activities that sequester carbon181,182. However, challenges in accurately documenting sequestered carbon and integrating land-use activities into emissions trading highlight the need for robust Measurement, Reporting, and Verification (MRV) systems182.
To overcome these challenges, future policies must adopt an integrated, long-term approach that aligns soil moisture management with broader climate goals. First, policies should shift focus from short-term agricultural outputs to practices that promote soil health and long-term carbon sequestration. Moreover, integrating nutrient management practices, like composting and organic amendments, can further contribute to climate-smart soil management183,184. Incentive frameworks should also be refined to encourage the adoption of climate-smart agricultural practices. Financial incentives such as carbon taxes, subsidies, and carbon credit offsets can be powerful tools, but they must be carefully designed to avoid unintended consequences, like increased emissions from certain management practices176. Additionally, the development of localized soil information systems can provide tailored data on soil conditions and carbon sequestration potential, enhancing the precision and effectiveness of soil moisture management strategies. Engaging key stakeholders, including farmers, policymakers, and scientists, in the design and implementation of these policies will be essential for fostering widespread adoption and ensuring their success.
Conclusion
This review has demonstrated the pivotal role of soil moisture in regulating CS-GHG. Soil moisture directly influences plant photosynthesis and respiration, soil microbial activity, and soil organic matter decomposition, with optimal levels enhancing these processes and increasing carbon sequestration. However, extremes in soil moisture disrupt these mechanisms, reducing sequestration efficiency. CO2 emissions exhibit a "Peak and Decline" pattern, peaking at around 40% WFPS, while CH4 and N2O emissions peak at higher levels, between 60% and 80% WFPS for CH4 and around 80% WFPS for N2O, highlighting the need for targeted soil moisture management. Droughts reduce soil moisture, limiting carbon sequestration and altering GHG emissions, while floods create anaerobic conditions favorable for CH4 production. Sustainable land management practices such as conservation agriculture, agroforestry, and optimized water management are crucial for enhancing carbon sequestration and reducing GHG emissions by improving soil structure and maintaining optimal moisture levels. Moreover, improving the accuracy of soil moisture and CS-GHG simulations hinges on enhancing high-resolution multiscale observations and refining feedback modeling. Integrating remote sensing technologies with expanded ground-based observations, along with employing hybrid modeling frameworks can significantly boost predictive capabilities while addressing data and feedback modeling challenges. Additionally, iterative model-experiment approaches, such as the ModEx framework, play a crucial role in linking observational data with models, enabling continuous refinement and strengthening the predictive power of CS-GHG models. Furthermore, current policies and incentives need to be better aligned with long-term climate goals to enhance soil moisture management for both carbon storage and the reduction of GHG emissions. Addressing these challenges through interdisciplinary approaches and innovative technologies will be essential in mitigating climate change and promoting sustainable land management practices.
References
Torres, C. M. M. E. et al. Greenhouse gas emissions and carbon sequestration by agroforestry systems in southeastern Brazil. Sci. Rep. 7, 16738 (2017).
Badiou, P., McDougal, R., Pennock, D. & Clark, B. Greenhouse gas emissions and carbon sequestration potential in restored wetlands of the Canadian prairie pothole region. Wetl. Ecol. Manag 19, 237–256 (2011).
Sha, Z. et al. The global carbon sink potential of terrestrial vegetation can be increased substantially by optimal land management. Commun. Earth Environ. 3, 8 (2022).
Lal, R. Carbon sequestration in dryland ecosystems. Environ. Manag. 33, 528–544 (2004).
Hudson, B. D. Soil organic matter and available water capacity. J. Soil Water Conserv 49, 189 (1994).
Pan, G., Smith, P. & Pan, W. The role of soil organic matter in maintaining the productivity and yield stability of cereals in China. Agric Ecosyst. Environ. 129, 344–348 (2009).
Paustian, K. et al. Climate-smart soils. Nature 532, 49–57 (2016).
Lal, R. Carbon sequestration. Philos. Trans. R. Soc. B: Biol. Sci. 363, 815–830 (2008).
Houghton, R. A. Balancing the global carbon budget. Annu Rev. Earth Planet Sci. 35, 313–347 (2007).
Lal, R. Soil carbon sequestration impacts on global climate change and food security. Science (1979) 304, 1623–1627 (2004).
Liu, L. & Greaver, T. L. A review of nitrogen enrichment effects on three biogenic GHGs: the CO2 sink may be largely offset by stimulated N2O and CH4 emission. Ecol. Lett. 12, 1103–1117 (2009).
Tian, H. et al. The terrestrial biosphere as a net source of greenhouse gases to the atmosphere. Nature 531, 225–228 (2016).
Shcherbak, I., Millar, N. & Robertson, G. P. Global metaanalysis of the nonlinear response of soil nitrous oxide (N2O) emissions to fertilizer nitrogen. Proc. Natl Acad. Sci. 111, 9199–9204 (2014).
Were, D., Kansiime, F., Fetahi, T., Cooper, A. & Jjuuko, C. Carbon sequestration by wetlands: a critical review of enhancement measures for climate change mitigation. Earth Syst. Environ. 3, 327–340 (2019).
Smith, P. et al. Chapter 11 - Agriculture, forestry and other land use (AFOLU). in Climate Change 2014: Mitigation of Climate Change. IPCC Working Group III Contribution to AR5 (Cambridge University Press, 2014).
Camino‐Serrano, M. et al. Linking variability in soil solution dissolved organic carbon to climate, soil type, and vegetation type. Glob. Biogeochem. Cycles 28, 497–509 (2014).
Alidoust, E., Afyuni, M., Hajabbasi, M. A. & Mosaddeghi, M. R. Soil carbon sequestration potential as affected by soil physical and climatic factors under different land uses in a semiarid region. Catena (Amst.) 171, 62–71 (2018).
Fang, J., Yu, G., Liu, L., Hu, S. & Chapin, F. S. III Climate change, human impacts, and carbon sequestration in China. Proc. Natl Acad. Sci. 115, 4015–4020 (2018).
Poblador, S., Lupon, A., Sabaté, S. & Sabater, F. Soil water content drives spatiotemporal patterns of CO2 and N2O emissions from a Mediterranean riparian forest soil. Biogeosciences 14, 4195–4208 (2017).
Liang, L. L., Grantz, D. A. & Jenerette, G. D. Multivariate regulation of soil CO2 and N2O pulse emissions from agricultural soils. Glob. Chang Biol. 22, 1286–1298 (2016).
Schaufler, G. et al. Greenhouse gas emissions from European soils under different land use: effects of soil moisture and temperature. Eur. J. Soil Sci. 61, 683–696 (2010).
Humphrey, V. et al. Soil moisture–atmosphere feedback dominates land carbon uptake variability. Nature 592, 65–69 (2021).
He, Y. et al. Response of GHG emissions to interactions of temperature and drying in the karst wetland of the Yunnan-Guizhou Plateau. Front Environ. Sci. 10, 973900 (2022).
Feng, X. & Wang, S. Plant influences on soil microbial carbon pump efficiency. Glob. Chang Biol. 29, 3854–3856 (2023).
Davenport, R. et al. Decomposition decreases molecular diversity and ecosystem similarity of soil organic matter. Proc. Natl Acad. Sci. 120, e2303335120 (2023).
Liu, L. et al. Soil moisture dominates dryness stress on ecosystem production globally. Nat. Commun. 11, 4892 (2020).
Yu, T. et al. Disentangling the relative effects of soil moisture and vapor pressure deficit on photosynthesis in dryland Central Asia. Ecol. Indic. 137, 108698 (2022).
Stocker, B. D. et al. Drought impacts on terrestrial primary production underestimated by satellite monitoring. Nat. Geosci. 12, 264–270 (2019).
Lv, G., Jin, J., He, M. & Wang, C. Soil moisture content dominates the photosynthesis of C3 and C4 plants in a desert steppe after long-term warming and increasing precipitation. Plants 12, 2903 (2023).
Huang, S. et al. Autotrophic and heterotrophic soil respiration responds asymmetrically to drought in a subtropical forest in the Southeast China. Soil Biol. Biochem 123, 242–249 (2018).
Balogh, J. et al. Autotrophic component of soil respiration is repressed by drought more than the heterotrophic one in dry grasslands. Biogeosciences 13, 5171–5182 (2016).
Sun, S., Lei, H. & Chang, S. X. Drought differentially affects autotrophic and heterotrophic soil respiration rates and their temperature sensitivity. Biol. Fertil. Soils 55, 275–283 (2019).
Chang, C.-T. et al. Does soil moisture overrule temperature dependence of soil respiration in Mediterranean riparian forests? Biogeosciences 11, 6173–6185 (2014).
Li, L. et al. Representation of plant hydraulics in the Noah‐MP land surface model: Model development and multiscale evaluation. J. Adv. Model Earth Syst. 13, e2020MS002214 (2021).
Joshi, J. et al. Towards a unified theory of plant photosynthesis and hydraulics. Nat. Plants 8, 1304–1316 (2022).
Brodribb, T. J., Feild, T. S. & Jordan, G. J. Leaf maximum photosynthetic rate and venation are linked by hydraulics. Plant Physiol. 144, 1890–1898 (2007).
Kuzyakov, Y. & Blagodatskaya, E. Microbial hotspots and hot moments in soil: Concept & review. Soil Biol. Biochem 83, 184–199 (2015).
Denardin, L. G. et al. How different soil moisture levels affect the microbial activity. Ciência Rural 50, e20190831 (2020).
Burke, D. J., Smemo, K. A., López-Gutiérrez, J. C. & DeForest, J. L. Soil fungi influence the distribution of microbial functional groups that mediate forest greenhouse gas emissions. Soil Biol. Biochem 53, 112–119 (2012).
Brockett, B. F. T., Prescott, C. E. & Grayston, S. J. Soil moisture is the major factor influencing microbial community structure and enzyme activities across seven biogeoclimatic zones in western Canada. Soil Biol. Biochem 44, 9–20 (2012).
Malyan, S. K. et al. Role of fungi in climate change abatement through carbon sequestration. Recent Advancement in White Biotechnology Through Fungi: Volume 3: Perspective for Sustainable Environments 283–295 (2019).
Liao, H. et al. Microbial autotrophy explains large‐scale soil CO2 fixation. Glob. Chang Biol. 29, 231–242 (2023).
Liu, Y. et al. Carbon input and allocation by rice into paddy soils: A review. Soil Biol. Biochem 133, 97–107 (2019).
Chen, Q., Long, C., Chen, J. & Cheng, X. Differential response of soil CO2, CH4, and N2O emissions to edaphic properties and microbial attributes following afforestation in central China. Glob. Chang Biol. 27, 5657–5669 (2021).
Fairbairn, L. et al. Relationship between soil CO2 fluxes and soil moisture: Anaerobic sources explain fluxes at high water content. Geoderma 434, 116493 (2023).
Kong, D. et al. Linking methane emissions to methanogenic and methanotrophic communities under different fertilization strategies in rice paddies. Geoderma 347, 233–243 (2019).
Chowdhury, T. R. & Dick, R. P. Ecology of aerobic methanotrophs in controlling methane fluxes from wetlands. Appl. soil Ecol. 65, 8–22 (2013).
He, P. et al. Straw addition and low soil moisture decreased temperature sensitivity and activation energy of soil organic matter. Geoderma 442, 116802 (2024).
Heckman, K. A. et al. Moisture-driven divergence in mineral-associated soil carbon persistence. Proc. Natl Acad. Sci. 120, e2210044120 (2023).
Kögel-Knabner, I. The macromolecular organic composition of plant and microbial residues as inputs to soil organic matter. Soil Biol. Biochem 34, 139–162 (2002).
Six, J., Conant, R. T., Paul, E. A. & Paustian, K. Stabilization mechanisms of soil organic matter: Implications for C-saturation of soils. Plant Soil 241, 155–176 (2002).
Bridgham, S. D., Cadillo-Quiroz, H., Keller, J. K. & Zhuang, Q. Methane emissions from wetlands: biogeochemical, microbial, and modeling perspectives from local to global scales. Glob. Chang Biol. 19, 1325–1346 (2013).
Utomo, W. H. & Dexter, A. R. Changes in soil aggregate water stability induced by wetting and drying cycles in non‐saturated soil. J. Soil Sci. 33, 623–637 (1982).
Lavee, H., Sarah, P. & Imeson, A. C. Aggregate stability dynamics as affected by soil temperature and moisture regimes. Geografiska Annaler: Ser. A, Phys. Geogr. 78, 73–82 (1996).
Ofiti, N. O. E. et al. Warming promotes loss of subsoil carbon through accelerated degradation of plant-derived organic matter. Soil Biol. Biochem 156, 108185 (2021).
Curiel Yuste, J. et al. Microbial soil respiration and its dependency on carbon inputs, soil temperature and moisture. Glob. Chang Biol. 13, 2018–2035 (2007).
Li, J., Wang, G., Allison, S. D., Mayes, M. A. & Luo, Y. Soil carbon sensitivity to temperature and carbon use efficiency compared across microbial-ecosystem models of varying complexity. Biogeochemistry 119, 67–84 (2014).
Yang, L. et al. Soil microbial respiration adapts to higher and longer warming experiments at the global scale. Environ. Res. Lett. 18, 034044 (2023).
Dacal, M., Bradford, M. A., Plaza, C., Maestre, F. T. & García-Palacios, P. Soil microbial respiration adapts to ambient temperature in global drylands. Nat. Ecol. Evol. 3, 232–238 (2019).
Li, H. et al. Field-scale assessment of direct and indirect effects of soil texture on organic matter mineralization during a dry summer. Sci. Total Environ. 899, 165749 (2023).
Feng, X. et al. Nitrogen input enhances microbial carbon use efficiency by altering plant–microbe–mineral interactions. Glob. Chang Biol. 28, 4845–4860 (2022).
Yao, Z. et al. Soil C/N ratio is the dominant control of annual N2O fluxes from organic soils of natural and semi-natural ecosystems. Agric Meteorol. 327, 109198 (2022).
Mu, Z., Huang, A., Ni, J. & Xie, D. Linking annual N2O emission in organic soils to mineral nitrogen input as estimated by heterotrophic respiration and soil C/N ratio. PLoS One 9, e96572 (2014).
Malik, A. A. et al. Land use driven change in soil pH affects microbial carbon cycling processes. Nat. Commun. 9, 3591 (2018).
Craine, J. M. & Gelderman, T. M. Soil moisture controls on temperature sensitivity of soil organic carbon decomposition for a mesic grassland. Soil Biol. Biochem 43, 455–457 (2011).
García‐Marco, S. et al. Ranking factors affecting emissions of GHG from incubated agricultural soils. Eur. J. Soil Sci. 65, 573–583 (2014).
Green, J. K. et al. Large influence of soil moisture on long-term terrestrial carbon uptake. Nature 565, 476–479 (2019).
Tagesson, T. et al. Very high CO2 exchange fluxes at the peak of the rainy season in a West African grazed semi-arid savanna ecosystem. Geografisk Tidsskr.-Dan. J. Geogr. 116, 93–109 (2016).
Ardö, J., Mölder, M., El-Tahir, B. A. & Elkhidir, H. A. M. Seasonal variation of carbon fluxes in a sparse savanna in semi arid Sudan. Carbon Balance Manag 3, 7 (2008).
Zona, D. et al. Pan-Arctic soil moisture control on tundra carbon sequestration and plant productivity. Glob. Chang Biol. 29, 1267–1281 (2023).
Phillips, O. L. et al. Drought sensitivity of the Amazon rainforest. Science (1979) 323, 1344–1347 (2009).
Liu, Y. et al. Impacts of droughts on carbon sequestration by China’s terrestrial ecosystems from 2000 to 2011. Biogeosciences 11, 2583–2599 (2014).
Ge, X. et al. Imposed drought effects on carbon storage of moso bamboo ecosystem in southeast China: results from a field experiment. Ecol. Res 33, 393–402 (2018).
Leifeld, J. & Menichetti, L. The underappreciated potential of peatlands in global climate change mitigation strategies. Nat. Commun. 9, 1071 (2018).
Hanson, P. J. et al. Rapid net carbon loss from a whole-ecosystem warmed peatland. AGU Adv. 1, e2020AV000163 (2020).
Matyshak, G. V. et al. Influence of moisture on the CO2 flux from Palsa mire soils in the North of Western Siberia. Eurasia. Soil Sci. 56, 434–446 (2023).
Haverd, V., Smith, B. & Trudinger, C. Dryland vegetation response to wet episode, not inherent shift in sensitivity to rainfall, behind Australia’s role in 2011 global carbon sink anomaly. Glob. Chang Biol. 22, 2315–2316 (2016).
Li, Y. et al. Trends in drought and effects on carbon sequestration over the Chinese mainland. Sci. Total Environ. 856, 159075 (2023).
Tomar, U. & Baishya, R. Moisture regime influence on soil carbon stock and carbon sequestration rates in semi-arid forests of the National Capital Region, India. J. Res (Harbin) 31, 2323–2332 (2020).
Yang, F. et al. Desert abiotic carbon sequestration weakening by precipitation. Environ. Sci. Technol. 57, 7174–7184 (2023).
Marhan, S., Kandeler, E., Rein, S., Fangmeier, A. & Niklaus, P. A. Indirect effects of soil moisture reverse soil C sequestration responses of a spring wheat agroecosystem to elevated CO2. Glob. Chang Biol. 16, 469–CO483 (2010).
Gamage, D. et al. New insights into the cellular mechanisms of plant growth at elevated atmospheric carbon dioxide concentrations. Plant Cell Environ. 41, 1233–1246 (2018).
Khalil, M. I. & Baggs, E. M. CH4 oxidation and N2O emissions at varied soil water-filled pore spaces and headspace CH4 concentrations. Soil Biol. Biochem 37, 1785–1794 (2005).
Sey, B. K., Manceur, A. M., Whalen, J. K., Gregorich, E. G. & Rochette, P. Small-scale heterogeneity in carbon dioxide, nitrous oxide and methane production from aggregates of a cultivated sandy-loam soil. Soil Biol. Biochem 40, 2468–2473 (2008).
Li, Y., Chen, Y. & Wu, J. Enhancement of methane production in anaerobic digestion process: A review. Appl Energy 240, 120–137 (2019).
Hou, H., Peng, S., Xu, J., Yang, S. & Mao, Z. Seasonal variations of CH4 and N2O emissions in response to water management of paddy fields located in Southeast China. Chemosphere 89, 884–892 (2012).
Christiansen, J. R., Vesterdal, L. & Gundersen, P. Nitrous oxide and methane exchange in two small temperate forest catchments—effects of hydrological gradients and implications for global warming potentials of forest soils. Biogeochemistry 107, 437–454 (2012).
Wu, X., Brüggemann, N., Butterbach-Bahl, K., Fu, B. & Liu, G. Snow cover and soil moisture controls of freeze–thaw-related soil gas fluxes from a typical semi-arid grassland soil: a laboratory experiment. Biol. Fertil. Soils 50, 295–306 (2014).
Liu, Y. et al. Effects of freeze-thaw cycles on soil greenhouse gas emissions: A systematic review. Environ. Res. 248, 118386 (2024).
Haro, K. et al. Assessment of CH4 and CO2 surface emissions from Polesgo’s landfill (Ouagadougou, Burkina Faso) based on static chamber method. Adv. Clim. Change Res. 10, 181–191 (2019).
Osei, A. K., Rezanezhad, F. & Oelbermann, M. Impact of freeze-thaw cycles on greenhouse gas emissions in marginally productive agricultural land under different perennial bioenergy crops. J. Environ. Manag. 357, 120739 (2024).
Min, Y. et al. Flooding lowers the emissions of CO2 and CH4 during the freeze-thaw process in a lacustrine wetland. Catena (Amst.) 227, 107132 (2023).
Yang, S., He, Z. & Chen, L. Different responses of CO2 and CH4 to freeze-thaw cycles in an alpine forest ecosystem in northwestern China. Sci. Total Environ. 863, 160886 (2023).
Wu, X. et al. Soil properties mediate the freeze-thaw-related soil N2O and CO2 emissions from temperate grasslands. Catena (Amst.) 195, 104797 (2020).
Metze, D. et al. Microbial growth under drought is confined to distinct taxa and modified by potential future climate conditions. Nat. Commun. 14, 5895 (2023).
Warren, C. R. & Manzoni, S. When dry soil is re-wet, trehalose is respired instead of supporting microbial growth. Soil Biol. Biochem 184, 109121 (2023).
Barnard, R. L., Blazewicz, S. J. & Firestone, M. K. Rewetting of soil: revisiting the origin of soil CO2 emissions. Soil Biol. Biochem 147, 107819 (2020).
Sang, J., Lakshani, M. M. T., Chamindu Deepagoda, T. K. K., Shen, Y. & Li, Y. Drying and rewetting cycles increased soil carbon dioxide rather than nitrous oxide emissions: A meta-analysis. J. Environ. Manag. 324, 116391 (2022).
Zou, J. et al. Rewetting global wetlands effectively reduces major greenhouse gas emissions. Nat. Geosci. 15, 627–632 (2022).
White, M. A., Thornton, P. E., Running, S. W. & Nemani, R. R. Parameterization and sensitivity analysis of the BIOME–BGC terrestrial ecosystem model: Net primary production controls. Earth Interact. 4, 1–85 (2000).
Gilhespy, S. L. et al. First 20 years of DNDC (DeNitrification DeComposition): model evolution. Ecol. Model. 292, 51–62 (2014).
Parton, W. J. The CENTURY model. in Evaluation of soil organic matter models: Using existing long-term datasets 283–291 (Springer, 1996).
Krinner, G. et al. A dynamic global vegetation model for studies of the coupled atmosphere-biosphere system. Glob. Biogeochem Cycles 19, GB1015 (2005).
Hickler, T. et al. Using a generalized vegetation model to simulate vegetation dynamics in northeastern USA. Ecology 85, 519–530 (2004).
Lawrence, D. M. et al. The community land model version 5: description of new features, benchmarking, and impact of forcing uncertainty. J. Adv. Model Earth Syst. 11, 4245–4287 (2019).
Burrows, S. M. et al. The DOE E3SM v1.1 Biogeochemistry configuration: description and simulated ecosystem-climate responses to historical changes in forcing. J. Adv. Model Earth Syst. 12, e2019MS001766 (2020).
Tian, H. et al. North American terrestrial CO2 uptake largely offset by CH4 and N2O emissions: toward a full accounting of the greenhouse gas budget. Clim. Change 129, 413–426 (2015).
Tian, H. et al. Net exchanges of CO2, CH4, and N2O between China's terrestrial ecosystems and the atmosphere and their contributions to global climate warming. J. Geophys. Res. Biogeosci. 116, G02011 (2011).
Dai, Y. et al. The Common Land Model. Bull. Am. Meteorol. Soc. 84, 1013–1024 (2003).
Govind, A. et al. A spatially explicit hydro-ecological modeling framework (BEPS-TerrainLab V2.0): Model description and test in a boreal ecosystem in Eastern North America. J. Hydrol. (Amst.) 367, 200–216 (2009).
Salmon, E. et al. Assessing methane emissions for northern peatlands in ORCHIDEE-PEAT revision 7020. Geosci. Model Dev. 15, 2813–2838 (2022).
Kallingal, J. T. et al. Optimising CH_4 simulations from the LPJ-GUESS model v4.1 using an adaptive Markov chain Monte Carlo algorithm. Geosci. Model Dev. 17, 2299–2324 (2024).
Hobbs, P. R., Sayre, K. & Gupta, R. The role of conservation agriculture in sustainable agriculture. Philos. Trans. R. Soc. B: Biol. Sci. 363, 543–555 (2008).
Franzluebbers, A. J. Achieving Soil Organic Carbon Sequestration with Conservation Agricultural Systems in the Southeastern United States. Soil Sci. Soc. Am. J. 74, 347–357 (2010).
Hartwig, N. L. & Ammon, H. U. Cover crops and living mulches. Weed Sci. 50, 688–699 (2002).
Lal, R. Soil carbon sequestration and aggregation by cover cropping. J. Soil Water Conserv 70, 329 (2015).
Kahlon, M. S., Lal, R. & Ann-Varughese, M. Twenty two years of tillage and mulching impacts on soil physical characteristics and carbon sequestration in Central Ohio. Soil Tillage Res 126, 151–158 (2013).
Yadav, G. S. et al. Conservation tillage and nutrient management effects on productivity and soil carbon sequestration under double cropping of rice in north eastern region of India. Ecol. Indic. 105, 303–315 (2019).
Ramachandran Nair, P. K., Mohan Kumar, B. & Nair, V. D. Agroforestry as a strategy for carbon sequestration. J. Plant Nutr. Soil Sci. 172, 10–23 (2009).
Jose, S. Agroforestry for ecosystem services and environmental benefits: an overview. Agrofor. Syst. 76, 1–10 (2009).
Lin, B. B. The role of agroforestry in reducing water loss through soil evaporation and crop transpiration in coffee agroecosystems. Agric Meteorol. 150, 510–518 (2010).
Ghosh, S., Wilson, B., Ghoshal, S., Senapati, N. & Mandal, B. Organic amendments influence soil quality and carbon sequestration in the Indo-Gangetic plains of India. Agric Ecosyst. Environ. 156, 134–141 (2012).
Xie, X. et al. Effects of atmospheric aerosols on terrestrial carbon fluxes and CO2 concentrations in China. Atmos. Res 237, 104859 (2020).
Kok, J. F. et al. Mineral dust aerosol impacts on global climate and climate change. Nat. Rev. Earth Environ. 4, 71–86 (2023).
Auffhammer, M., Ramanathan, V. & Vincent, J. R. Integrated model shows that atmospheric brown clouds and greenhouse gases have reduced rice harvests in India. Proc. Natl Acad. Sci. 103, 19668–19672 (2006).
Lampayan, R. M., Rejesus, R. M., Singleton, G. R. & Bouman, B. A. M. Adoption and economics of alternate wetting and drying water management for irrigated lowland rice. Field Crops Res 170, 95–108 (2015).
Chidthaisong, A. et al. Evaluating the effects of alternate wetting and drying (AWD) on methane and nitrous oxide emissions from a paddy field in Thailand. Soil Sci. Plant Nutr. 64, 31–38 (2018).
Zhe, G. et al. Irrigation scheduling approaches and applications: a review. J. Irrig. Drain. Eng. 146, 04020007 (2020).
Gultekin, R. et al. Effect of deficit irrigation practices on greenhouse gas emissions in drip irrigation. Sci. Hortic. 310, 111757 (2023).
Cayuela, M. L. et al. Biochar and denitrification in soils: when, how much and why does biochar reduce N2O emissions? Sci. Rep. 3, 1732 (2013).
Ulaby, F. T. & Batlivala, P. P. Optimum radar parameters for mapping soil moisture. IEEE Trans. Geosci. Electron. 14, 81–93 (1976).
Millard, K. & Richardson, M. Quantifying the relative contributions of vegetation and soil moisture conditions to polarimetric C-Band SAR response in a temperate peatland. Remote Sens Environ. 206, 123–138 (2018).
Balenzano, A. et al. Sentinel-1 soil moisture at 1 km resolution: a validation study. Remote Sens Environ. 263, 112554 (2021).
Zappa, L. et al. Detection and quantification of irrigation water amounts at 500 m using Sentinel-1 surface soil moisture. Remote Sens. 13, 1727 (2021).
Gao, Q., Zribi, M., Escorihuela, M. J. & Baghdadi, N. Synergetic use of Sentinel-1 and Sentinel-2 data for soil moisture mapping at 100 m resolution. Sensors 17, 1966 (2017).
Ågren, A. M., Larson, J., Paul, S. S., Laudon, H. & Lidberg, W. Use of multiple LIDAR-derived digital terrain indices and machine learning for high-resolution national-scale soil moisture mapping of the Swedish forest landscape. Geoderma 404, 115280 (2021).
Jin, J. et al. Support vector regression for high-resolution beach surface moisture estimation from terrestrial LiDAR intensity data. Int. J. Appl. Earth Obs. Geoinf. 102, 102458 (2021).
Liu, A., Cheng, X. & Chen, Z. Performance evaluation of GEDI and ICESat-2 laser altimeter data for terrain and canopy height retrievals. Remote Sens Environ. 264, 112571 (2021).
Ma, L. et al. Spatial heterogeneity of global forest aboveground carbon stocks and fluxes constrained by spaceborne lidar data and mechanistic modeling. Glob. Chang Biol. 29, 3378–3394 (2023).
Lal, P. et al. A multi-scale algorithm for the NISAR mission high-resolution soil moisture product. Remote Sens Environ. 295, 113667 (2023).
Kemppinen, J., Niittynen, P., Riihimäki, H. & Luoto, M. Modelling soil moisture in a high-latitude landscape using LiDAR and soil data. Earth Surf. Process Land. 43, 1019–1031 (2018).
Baldocchi, D. et al. FLUXNET: A new tool to study the temporal and spatial variability of ecosystem-scale carbon dioxide, water vapor, and energy flux densities. Bull. Am. Meteorol. Soc. 82, 2415–2434 (2001).
Williams, M. et al. Improving land surface models with FLUXNET data. Biogeosciences 6, 1341–1359 (2009).
Chambers, J. et al. Next Generation Ecosystem Experiment (NGEE) Tropics. US DOE NGEE Tropics White Paper (2014).
Wullschleger, S. D. Support for Next-Generation Ecosystem Experiments (NGEE Arctic) Field Campaign Report. (2019).
Hanson, P. J. et al. Intermediate-scale community-level flux of CO2 and CH4 in a Minnesota peatland: putting the SPRUCE project in a global context. Biogeochemistry 129, 255–272 (2016).
Wu, X., Xiao, Q., Wen, J., You, D. & Hueni, A. Advances in quantitative remote sensing product validation: Overview and current status. Earth Sci. Rev. 196, 102875 (2019).
Tenan, S., Pedrini, P., Bragalanti, N., Groff, C. & Sutherland, C. Data integration for inference about spatial processes: A model-based approach to test and account for data inconsistency. PLoS One 12, e0185588 (2017).
Chave, J. et al. Ground data are essential for biomass remote sensing missions. Surv. Geophys 40, 863–880 (2019).
Babaeian, E. et al. Ground, proximal, and satellite remote sensing of soil moisture. Rev. Geophys. 57, 530–616 (2019).
Von Arx, G., Dobbertin, M. & Rebetez, M. Spatio-temporal effects of forest canopy on understory microclimate in a long-term experiment in Switzerland. Agric Meteorol. 166, 144–155 (2012).
Zhang, K. et al. The sensitivity of North American terrestrial carbon fluxes to spatial and temporal variation in soil moisture: An analysis using radar‐derived estimates of root‐zone soil moisture. J. Geophys. Res. Biogeosci. 124, 3208–3231 (2019).
Védère, C. et al. How does soil water status influence the fate of soil organic matter? A review of processes across scales. Earth Sci. Rev. 234, 104214 (2022).
Li, N., Skaggs, T. H., Ellegaard, P., Bernal, A. & Scudiero, E. Relationships among soil moisture at various depths under diverse climate, land cover and soil texture. Sci. Total Environ. 947, 174583 (2024).
Mimeau, L. et al. Modeling the response of soil moisture to climate variability in the Mediterranean region. Hydrol. Earth Syst. Sci. Discuss. 2020, 1–29 (2020).
Manzoni, S., Schimel, J. P. & Porporato, A. Responses of soil microbial communities to water stress: results from a meta‐analysis. Ecology 93, 930–938 (2012).
Fisher, R. A. & Koven, C. D. Perspectives on the future of land surface models and the challenges of representing complex terrestrial systems. J. Adv. Model Earth Syst. 12, e2018MS001453 (2020).
O’Connell, C. S., Ruan, L. & Silver, W. L. Drought drives rapid shifts in tropical rainforest soil biogeochemistry and greenhouse gas emissions. Nat. Commun. 9, 1348 (2018).
Kosten, S. et al. Extreme drought boosts CO2 and CH4 emissions from reservoir drawdown areas. Inland Waters 8, 329–340 (2018).
Anderegg, W. R. L. et al. Pervasive drought legacies in forest ecosystems and their implications for carbon cycle models. Science 349, 528–532 (2015).
Green, J. K. et al. Regionally strong feedbacks between the atmosphere and terrestrial biosphere. Nat. Geosci. 10, 410–414 (2017).
Blyth, E. M. et al. Advances in land surface modelling. Curr. Clim. Change Rep. 7, 45–71 (2021).
Flato, G. M. Earth system models: an overview. Wiley Interdiscip. Rev. Clim. Change 2, 783–800 (2011).
Müller-Hansen, F. et al. Towards representing human behavior and decision making in Earth system models–an overview of techniques and approaches. Earth Syst. Dyn. 8, 977–1007 (2017).
Kyker-Snowman, E. et al. Increasing the spatial and temporal impact of ecological research: A roadmap for integrating a novel terrestrial process into an Earth system model. Glob. Chang Biol. 28, 665–684 (2022).
Moore, D. J. P. A framework for incorporating ecology into Earth System Models is urgently needed. Glob. Chang Biol. 28, 343–345 (2022).
Eyring, V. et al. Pushing the frontiers in climate modelling and analysis with machine learning. Nat. Clim. Chang. 14, 916–928 (2024).
Liu, L. et al. Knowledge-guided machine learning can improve carbon cycle quantification in agroecosystems. Nat. Commun. 15, 357 (2024).
Yang, Q. et al. A flexible and efficient knowledge-guided machine learning data assimilation (KGML-DA) framework for agroecosystem prediction in the US Midwest. Remote Sens Environ. 299, 113880 (2023).
Irrgang, C. et al. Towards neural Earth system modelling by integrating artificial intelligence in Earth system science. Nat. Mach. Intell. 3, 667–674 (2021).
Geer, A. J. Learning earth system models from observations: machine learning or data assimilation? Philos. Trans. R. Soc. A 379, 20200089 (2021).
Gruber, A. et al. Validation practices for satellite soil moisture retrievals: What are (the) errors? Remote Sens Environ. 244, 111806 (2020).
Ekardt, F., Wieding, J., Garske, B. & Stubenrauch, J. Agriculture-related climate policies-law and governance issues on the European and global level. CCLR 12, 316 (2018).
Salinas, J., Meca, D. & del Moral, F. Short-term effects of changing soil management practices on soil quality indicators and crop yields in greenhouses. Agronomy 10, 582 (2020).
Jacobs, A. A. et al. Cover crops and no-tillage reduce crop production costs and soil loss, compensating for lack of short-term soil quality improvement in a maize and soybean production system. Soil Tillage Res. 218, 105310 (2022).
Ogle, S. M. et al. Policy challenges to enhance soil carbon sinks: the dirty part of making contributions to the Paris agreement by the United States. Carbon Manag. 14, 2268071 (2023).
Zuo, Z. et al. Importance of soil moisture conservation in mitigating climate change. Sci. Bull. 69, 1332–1341 (2024).
He, T. et al. Meta-analysis shows the impacts of ecological restoration on greenhouse gas emissions. Nat. Commun. 15, 2668 (2024).
Grima, N., Singh, S. J., Smetschka, B. & Ringhofer, L. Payment for Ecosystem Services (PES) in Latin America: Analysing the performance of 40 case studies. Ecosyst. Serv. 17, 24–32 (2016).
Stubbs, M. Environmental Quality Incentives Program (EQIP): Status and Issues. (Congressional Research Service Washington, DC, USA, 2010).
Paul, C. et al. Carbon farming: are soil carbon certificates a suitable tool for climate change mitigation? J. Environ. Manag. 330, 117142 (2023).
Liu, L., Chen, C., Zhao, Y. & Zhao, E. China׳ s carbon-emissions trading: Overview, challenges and future. Renew. Sustain. Energy Rev. 49, 254–266 (2015).
Zougmoré, R., Jalloh, A. & Tioro, A. Climate-smart soil water and nutrient management options in semiarid West Africa: a review of evidence and analysis of stone bunds and zaï techniques. Agric Food Secur 3, 1–8 (2014).
Chowdhury, S. et al. Role of cultural and nutrient management practices in carbon sequestration in agricultural soil. Adv. Agron. 166, 131–196 (2021).
Anthony, T. L. & Silver, W. L. Hot moments drive extreme nitrous oxide and methane emissions from agricultural peatlands. Glob. Chang Biol. 27, 5141–5153 (2021).
Adviento-Borbe, M. A. et al. Methane and nitrous oxide emissions from flooded rice systems following the end-of-season drain. J. Environ. Qual. 44, 1071–1079 (2015).
Adviento-Borbe, M. A. A., Haddix, M. L., Binder, D. L., Walters, D. T. & Dobermann, A. Soil greenhouse gas fluxes and global warming potential in four high-yielding maize systems. Glob. Chang Biol. 13, 1972–1988 (2007).
Burger, M. et al. Microbial responses and nitrous oxide emissions during wetting and drying of organically and conventionally managed soil under tomatoes. Biol. Fertil. Soils 42, 109–118 (2005).
Davidson, E. A., Keller, M., Erickson, H. E., Verchot, L. V. & Veldkamp, E. Testing a conceptual model of soil emissions of nitrous and nitric oxides: Using two functions based on soil nitrogen availability and soil water content, the hole-in-the-pipe model characterizes a large fraction of the observed variation of nitric oxide and nitrous oxide emissions from soils. Bioscience 50, 667–680 (2000).
Wu, H., Xingkai, X., Cheng, W. & Lin, H. Dissolved organic matter and inorganic N jointly regulate greenhouse gases fluxes from forest soils with different moistures during a freeze-thaw period. Soil Sci. Plant Nutr. 66, 163–176 (2020).
Yanai, Y., Toyota, K. & Okazaki, M. Effects of charcoal addition on N2O emissions from soil resulting from rewetting air-dried soil in short-term laboratory experiments. Soil Sci. Plant Nutr. 53, 181–188 (2007).
Acknowledgements
This research is supported by the Reducing Uncertainties in Biogeochemical Interactions through Synthesis and Computation Science Focus Area (RUBISCO SFA) project funded through the Earth and Environmental Systems Sciences Division of the Biological and Environmental Research Office in the US Department of Energy (DOE) Office of Science. Oak Ridge National Laboratory (ORNL) is supported by the Office of Science of the DOE under Contract No. DE-AC05-00OR22725. This research is also an outcome of the Soil Moisture Working Group supported by ORNL RUBISCO SFA. YF, LL, and MS are supported by the Earth and Biological Sciences Directorate (EBSD)’s Laboratory Directed Research and Development (LDRD) Program at Pacific Northwest National Laboratory (PNNL). PNNL is a multi-program national laboratory operated for the U.S. Department of Energy (DOE) by Battelle Memorial Institute under Contract No. DE-AC05-76RL01830. J.G.L. acknowledges the funding from USMILE European Research Council (ERC CU18-3746).
Author information
Authors and Affiliations
Contributions
Y.F.H. and J.F.M. conceived the idea and wrote the manuscript. G.K., J.G.L., L.C.L., M.A., M.J.S., S.K., X.Y.S., Y.P.W., and Y.L.F. contributed to the framework of the manuscript and participated in the writing process. H.Q.T. contributed to the model review section. C.M.B., J.T., J.Y.T., L.B.L., M.Z.J., Q.Z., F.M.H., H.S.C., X.Z., and Y.J.D. contributed to the manuscript and were instrumental in its revision and refinement.
Corresponding author
Ethics declarations
Competing interests
All authors declare no competing interests.
Additional information
Publisher’s note Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
Rights and permissions
Open Access This article is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License, which permits any non-commercial use, sharing, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if you modified the licensed material. You do not have permission under this licence to share adapted material derived from this article or parts of it. The images or other third party material in this article are included in the article’s Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by-nc-nd/4.0/.
About this article
Cite this article
Hao, Y., Mao, J., Bachmann, C.M. et al. Soil moisture controls over carbon sequestration and greenhouse gas emissions: a review. npj Clim Atmos Sci 8, 16 (2025). https://doi.org/10.1038/s41612-024-00888-8
Received:
Accepted:
Published:
DOI: https://doi.org/10.1038/s41612-024-00888-8
This article is cited by
-
Spatio-temporal variations in carbon sources, sinks and footprints of cropland ecosystems in the Middle and Lower Yangtze River Plain of China, 2013–2022
Scientific Reports (2025)
-
Conservation agriculture in mesic savannas: impact on soil organic carbon and nutrient stocks in Ghana
Environmental Earth Sciences (2025)
-
Decomposition dynamics and driving factors of leaf litter and fine roots decomposition in secondary oak forests following different management practices in Northwestern China
Plant and Soil (2025)