SEARCH · Search USGS

Results for “Carbon”

Search indexed USGS publications on groundwater, aquifers, geologic maps, mineral resources and earthquakes. Explore source records by subject and place.

SourceResearch connectionFrom yearThrough year

Quote a phrase for an exact phrase match. Source license links do not imply unrestricted reuse.

At least 343 records · Page 19Linked to original sources

USGS2018

A remote sensing-based model of tidal marsh aboveground carbon stocks for the conterminous United States

Remote sensing based maps of tidal marshes, both of their extents and carbon stocks, have the potential to play a key role in conducting greenhouse gas inventories and implementing climate mitigation policies. Our objective was to generate a single remote sensing model of tidal marsh aboveground biomass and carbon that represents nationally diverse tidal marshes within the conterminous United States (CONUS). We developed the first calibration-grade, national-scale dataset of aboveground tidal marsh biomass, species composition, and aboveground plant carbon content (%C) from six CONUS regions: Cape Cod, MA, Chesapeake Bay, MD, Everglades, FL, Mississippi Delta, LA, San Francisco Bay, CA, and Puget Sound, WA. Using the random forest machine learning algorithm, we tested whether imagery from multiple sensors, Sentinel-1 C-band synthetic aperture radar, Landsat, and the National Agriculture Imagery Program (NAIP), can improve model performance. The final model, driven by six Landsat vegetation indices and with the soil adjusted vegetation index as the most important (n = 409, RMSE = 310 g/m 2 , 10.3% normalized RMSE), successfully predicted biomass for a range of marsh plant functional types defined by height, leaf angle and growth form. Model results were improved by scaling field-measured biomass calibration data by NAIP-derived 30 m fraction green vegetation. With a mean plant carbon content of 44.1% (n = 1384, 95% C.I. = 43.99%–44.37%), we generated regional 30 m aboveground carbon density maps for estuarine and palustrine emergent tidal marshes as indicated by a modified NOAA Coastal Change Analysis Program map. We applied a multivariate delta method to calculate uncertainties in regional carbon densities and stocks that considered standard error in map area, mean biomass and mean %C. Louisiana palustrine emergent marshes had the highest C density (2.67 ± 0.004 Mg/ha) of all regions, while San Francisco Bay brackish/saline marshes had the highest C density of all estuarine emergent marshes (2.03 ± 0.004 Mg/ha). Estimated C stocks for predefined jurisdictional areas ranged from 1023 ± 39 Mg in the Nisqually National Wildlife Refuge in Washington to 507,761 ± 14,822 Mg in the Terrebonne and St. Mary Parishes in Louisiana. This modeling and data synthesis effort will allow for aboveground C stocks in tidal marshes to be included in the coastal wetland section of the U.S. National Greenhouse Gas Inventory. With the increased availability of free post-processed satellite data, we provide a tractable means of modeling tidal marsh aboveground biomass and carbon at the global extent as well.

ISPRS Journal of Photogrammetry and Remote Sensing↗

USGS2004

Sequestration of carbon in soil organic matter in Senegal: an overview

Sequestration of Carbon in Soil Organic Matter ( SOCSOM ) in Senegal is a multi-disciplinary development project planned and refined through two international workshops. The project was implemented by integrating a core of international experts in remote sensing, biogeochemical modeling, community socio-economic assessments, and carbon measurements in a fully collaborative manner with Senegal organizations, national scientists, and local knowledge and expertise. The study addresses the potential role developing countries in semi-arid areas can play in climate mitigation activities. Multiple benefits to smallholders could accrue as a result of management practices to re-establish soil carbon content lost because of land use changes or management practices that are not sustainable. The specific importance for the Sahel is because of the high vulnerability to climate change in already impoverished rural societies. The project focuses on four objectives in specific locations across the agroecological zones of Senegal. These objectives are: use of soil sampling and biogeochemical modeling to quantify the biophysical potential for carbon sequestration and to determine the sensitivity of the carbon stocks to various management and climate scenarios, to evaluate the socio-economic and cultural requirements necessary for successful project implementation directed toward an aggregation of smallholders to sequester around 100,000 t carbon (C), to support capacity building to develop a Carbon Specialist Team, and to initiate extrapolation from site-specific project areas to the Sahel region and the national level.

Journal of Arid Environments↗

USGS2018

Deciphering the dynamics of inorganic carbon export from intertidal salt marshes using high-frequency measurements

The lateral export of carbon from coastal marshes via tidal exchange is a key component of the marsh carbon budget and coastal carbon cycles. However, the magnitude of this export has been difficult to accurately quantify due to complex tidal dynamics and seasonal cycling of carbon. In this study, we use in situ , high-frequency measurements of dissolved inorganic carbon (DIC) and water fluxes to estimate lateral DIC fluxes from a U.S. northeastern salt marsh. DIC was measured by a CHANnelized Optical Sensor (CHANOS) that provided an in situ concentration measurement at 15-min intervals, during periods in summer (July – August) and late fall (December). Seasonal changes in the marsh had strong effects on DIC concentrations, while tidally-driven water fluxes were the fundamental vehicle of marsh carbon export. Episodic events, such as groundwater discharge and mean sea water level changes, can impact DIC flux through altered DIC concentrations and water flow. Variability between individual tides within each season was comparable to mean variability between the two seasons. Estimated mean DIC fluxes based on a multiple linear regression (MLR) model of DIC concentrations and high-frequency water fluxes agreed reasonably well with those derived from CHANOS DIC measurements for both study periods, indicating that high-frequency, modeled DIC concentrations, coupled with continuous water flux measurements and a hydrodynamic model, provide a robust estimate of DIC flux. Additionally, an analysis of sampling strategies revealed that DIC fluxes calculated using conventional sampling frequencies (hourly to two-hourly) of a single tidal cycle are unlikely to capture a representative mean DIC flux compared to longer-term measurements across multiple tidal cycles with sampling frequency on the order of tens of minutes. This results from a disproportionately large amount of the net DIC flux occurring over a small number of tidal cycles, while most tides have a near-zero DIC export. Thus, high-frequency measurements (on the order of tens of minutes or better) over the time period of interest are necessary to accurately quantify tidal exports of carbon species from salt marshes.

Marine Chemistry↗

USGS2024

Restoring blue carbon ecosystems

Mangroves, tidal marshes and seagrasses have experienced extensive historical reduction in extent due to direct and indirect effects of anthropogenic land use change. Habitat loss has contributed carbon emissions and led to foregone opportunities for carbon sequestration, which are disproportionately large due to high ‘blue carbon’ stocks and sequestration rates in these coastal ecosystems. As such, there has been a rapid increase in interest in using coastal habitat restoration as a climate change mitigation tool. This review shows that restoration efforts are able to substantially increase blue carbon stocks, while also having a positive impact on various gaseous fluxes. However, blue carbon increases are spatially variable, due to biophysical factors such as climate and geomorphic setting. While there are potentially hundreds of thousands of hectares of land that may be biophysically suitable for restoration, these activities are still often conducted at small scales and with mixed success. Maximizing potential carbon gains through blue carbon restoration will require managers and coastal planners to overcome the myriad socioeconomic and governance constraints related to land tenure, legislation, target setting and cost, which often push restoration projects into locations that are biophysically unsuitable for plant colonization.

Cambridge Prisms: Coastal Futures↗

USGS2000

Carbonate ions and arsenic dissolution by groundwater

Samples of Marshall Sandstone, a major source of groundwater with elevated arsenic levels in southeast Michigan, were exposed to bicarbonate ion under controlled chemical conditions. In particular, effects of pH and redox conditions on arsenic release were evaluated. The release of arsenic from the aquifer rock was strongly related to the bicarbonate concentration in the leaching solution. The results obtained suggest that the carbonation of arsenic sulfide minerals, including orpiment (As2S3) and realgar (As2S2), is an important process in leaching arsenic into groundwater under anaerobic conditions. The arseno-carbonate complexes formed, believed to be As(CO3)2-, As(CO3)(OH)2-, and AsCO3+, are stable in groundwater. The reaction of ferrous ion with the thioarsenite from carbonation process can result in the formation of arsenopyrite which is a common mineral in arsenic-rich aquifers.Samples of Marshall Sandstone, a major source of groundwater with elevated arsenic levels in southeast Michigan, were exposed to bicarbonate ion under controlled chemical conditions. In particular, effects of pH and redox conditions on arsenic release were evaluated. The release of arsenic from the aquifer rock was strongly related to the bicarbonate concentration in the leaching solution. The results obtained suggest that the carbonation of arsenic sulfide minerals, including orpiment (As2S3) and realgar (As2S2), is an important process in leaching arsenic into groundwater under anaerobic conditions. The arseno-carbonate complexes formed, believed to be As(CO3)2-, As(CO3)(OH)2-, and AsCO3+, are stable in groundwater. The reaction of ferrous ion with the thioarsenite from carbonation process can result in the formation of arsenopyrite which is a common mineral in arsenic-rich aquifers.The role of bicarbonate in leaching arsenic into groundwater was investigated by conducting batch experiments using core samples of Marshall Sandstone from southeast Michigan and different bicarbonate solutions. The effects of pH and redox conditions on As dissolution were examined. Results showed that As was not leached significantly out of the Marshall Sandstone samples after 3 d using either deionized water or groundwater, but As was leached efficiently by sodium bicarbonate, potassium bicarbonate, and ferric chloride solutions. The leaching rate with sodium bicarbonate was about 25% higher than that with potassium bicarbonate. The data indicated that bicarbonate ion was involved primarily in As dissolution and that hydroxyl radical ion did not affect As dissolution to any significant degree. The amount of As leached was dependent upon the sodium bicarbonate concentration, increasing with reaction time for each concentration. Significant As leaching was found in the extreme pH ranges of <1.9 and 8.0-10.4. The resulting arseno-carbonate complexes formed were stable in groundwater.

Environmental Science & Technology↗

USGS2001

Budgets of soil erosion and deposition for sediments and sedimentary organic carbon across the conterminous United States

The fate of soil organic matter during erosion and sedimentation has been difficult to assess because of the large size and complex turnover characteristics of the soil carbon reservoir. It has been assumed that most of the carbon released during erosion is lost to oxidation. Budgets of bulk soil and soil organic carbon erosion and deposition suggest that the primary fates of eroded soil carbon across the conterminous United States are trapping in impoundments and other redeposition. The total amount of soil carbon eroded and redeposited across the United States is ???0.04 Gt yr-1. Applying this revision to the U. S. carbon budget by Houghton et al. [1999] raises their net sequestration estimate by 20-47 %. If comparable rates of erosion and redeposition occur globally, net carbon sequestration would be ???1 Gt yr-1.

Global Biogeochemical Cycles↗

USGS2019

Remobilization of old permafrost carbon to Chukchi Sea sediments during the end of the last deglaciation

Climate warming is expected to destabilize permafrost carbon (PF‐C) by thaw‐erosion and deepening of the seasonally thawed active layer and thereby promote PF‐C mineralization to CO 2 and CH 4 . A similar PF‐C remobilization might have contributed to the increase in atmospheric CO 2 during deglacial warming after the last glacial maximum. Using carbon isotopes and terrestrial biomarkers (Δ 14 C, δ 13 C, and lignin phenols), this study quantifies deposition of terrestrial carbon originating from permafrost in sediments from the Chukchi Sea (core SWERUS‐L2‐4‐PC1). The sediment core reconstructs remobilization of permafrost carbon during the late Allerød warm period starting at 13,000 cal years before present (BP), the Younger Dryas, and the early Holocene warming until 11,000 cal years BP and compares this period with the late Holocene, from 3,650 years BP until present. Dual‐carbon‐isotope‐based source apportionment demonstrates that Ice Complex Deposit—ice‐ and carbon‐rich permafrost from the late Pleistocene (also referred to as Yedoma)—was the dominant source of organic carbon (66 ± 8%; mean ± standard deviation) to sediments during the end of the deglaciation, with fluxes more than twice as high (8.0 ± 4.6 g·m −2 ·year −1 ) as in the late Holocene (3.1 ± 1.0 g·m −2 ·year −1 ). These results are consistent with late deglacial PF‐C remobilization observed in a Laptev Sea record, yet in contrast with PF‐C sources, which at that location were dominated by active layer material from the Lena River watershed. Release of dormant PF‐C from erosion of coastal permafrost during the end of the last deglaciation indicates vulnerability of Ice Complex Deposit in response to future warming and sea level changes.

Global Biogeochemical Cycles↗

USGS2024

Clumped isotopes record a glacial-interglacial shift in seasonality of soil carbonate accumulation in the San Luis Valley, southern Rocky Mountains, USA

Clumped isotope paleothermometry using pedogenic carbonates is a powerful tool for investigating past climate changes. However, location-specific seasonal patterns of precipitation and soil moisture cause systematic biases in the temperatures they record, hampering comparison of data across large areas or differing climate states. To account for biases, more systematic studies of carbonate forming processes are needed. We measured modern soil temperatures within the San Luis Valley of the Rocky Mountains and compared them to paleotemperatures determined using clumped isotopes. For Holocene-age samples, clumped isotope results indicate carbonate accumulated at a range of temperatures with site averages similar to the annual mean. Paleotemperatures for late Pleistocene-age samples (ranging 19–72 ka in age) yielded site averages only 2°C lower, despite evidence that annual temperatures during glacial periods were 5–9°C colder than modern. We use a 1D numerical model of soil physics to support the idea that differences in hydrologic conditions in interglacial versus glacial periods promote differences in the seasonal distribution of soil carbonate accumulation. Model simulations of modern (Holocene) conditions suggest that soil drying under low soil p CO 2 favors year-round carbonate accumulation in this region but peaking during post-monsoon soil drying. During a “glacial” simulation with lowered temperatures and added snowpack, more carbonate accumulation shifted to the summer season. These experiments show that changing hydrologic regimes could change the seasonality of carbonate accumulation, which in this study blunts the use of clumped isotopes to quantify glacial-interglacial temperature changes. This highlights the importance of understanding seasonal biases of climate proxies for accurate paleoenvironmental reconstruction.

Colorado, new Mexico↗

USGS2026

Season and antecedent conditions impact concentration-discharge relationships for dissolved organic carbon and alkalinity in southeast Alaskan watershed

Fluvial export of dissolved carbon plays an important role in watershed-scale biogeochemistry. Predicted changes in climate are expected to impact watershed hydrologic regimes, and in turn, the sources and export of dissolved carbon from watersheds. Here, we utilize high resolution measurements of discharge and dissolved carbon concentration to examine how concentration-discharge (CQ) relationships vary seasonally and during high flow events over the main runoff season (May–October) in a temperate forested watershed in Southeast Alaska. Concentration-discharge relationships for dissolved organic carbon (DOC) and alkalinity demonstrated strong seasonal patterns, with more linear relationships in May and June versus other months. Changing power law model slopes ( b values; the exponent in a power law regression between runoff and carbon yields) indicated potentially shifting watershed sources (biogenic vs. geologic) and contrasting dominant flowpaths (shallow vs. deeper groundwater) for DOC and alkalinity over the sampling period. During the largest storm event of the study, DOC and alkalinity b values shifted from an overall pattern of transport (mean b = 1.58 values >1.0 indicate transport limitation) and source limitation (mean b = 0.48, values <1.0 indicate source limitation) to chemostatic (DOC, b = 0.99; alkalinity, b = 1.019). In June through August, patterns in hysteresis index suggest that CQ relationships were altered when storms followed in close succession to each other. Together, these findings indicate that seasonal and antecedent flow conditions play a role in dissolved carbon export from forested watersheds. Understanding these dynamics, particularly during winter months, will become increasingly important as changes to hydroclimate impact riverine carbon export.

Alaska↗

USGS2024

Biodiversity loss reduces global terrestrial carbon storage

Natural ecosystems store large amounts of carbon globally, as organisms absorb carbon from the atmosphere to build large, long-lasting, or slow-decaying structures such as tree bark or root systems. An ecosystem’s carbon sequestration potential is tightly linked to its biological diversity. Yet when considering future projections, many carbon sequestration models fail to account for the role biodiversity plays in carbon storage. Here, we assess the consequences of plant biodiversity loss for carbon storage under multiple climate and land-use change scenarios. We link a macroecological model projecting changes in vascular plant richness under different scenarios with empirical data on relationships between biodiversity and biomass. We find that biodiversity declines from climate and land use change could lead to a global loss of between 7.44-103.14 PgC (global sustainability scenario) and 10.87-145.95 PgC (fossil-fueled development scenario). This indicates a self-reinforcing feedback loop, where higher levels of climate change lead to greater biodiversity loss, which in turn leads to greater carbon emissions and ultimately more climate change. Conversely, biodiversity conservation and restoration can help achieve climate change mitigation goals.

Nature Communications↗

USGS2018

Latitudinal limits to the predicted increase of the peatland carbon sink with warming

The carbon sink potential of peatlands depends on the balance of carbon uptake by plants and microbial decomposition. The rates of both these processes will increase with warming but it remains unclear which will dominate the global peatland response. Here we examine the global relationship between peatland carbon accumulation rates during the last millennium and planetary-scale climate space. A positive relationship is found between carbon accumulation and cumulative photosynthetically active radiation during the growing season for mid- to high-latitude peatlands in both hemispheres. However, this relationship reverses at lower latitudes, suggesting that carbon accumulation is lower under the warmest climate regimes. Projections under Representative Concentration Pathway (RCP)2.6 and RCP8.5 scenarios indicate that the present-day global sink will increase slightly until around AD 2100 but decline thereafter. Peatlands will remain a carbon sink in the future, but their response to warming switches from a negative to a positive climate feedback (decreased carbon sink with warming) at the end of the twenty-first century.

Nature Climate Change↗

USGS2024

Vulnerability of mineral-associated soil organic carbon to climate across global drylands

Mineral-associated organic carbon (MAOC) constitutes a major fraction of global soil carbon and is assumed less sensitive to climate than particulate organic carbon (POC) due to protection by minerals. Despite its importance for long-term carbon storage, the response of MAOC to changing climates in drylands, which cover more than 40% of the global land area, remains unexplored. Here we assess topsoil organic carbon fractions across global drylands using a standardized field survey in 326 plots from 25 countries and 6 continents. We find that soil biogeochemistry explained the majority of variation in both MAOC and POC. Both carbon fractions decreased with increases in mean annual temperature and reductions in precipitation, with MAOC responding similarly to POC. Therefore, our results suggest that ongoing climate warming and aridification may result in unforeseen carbon losses across global drylands, and that the protective role of minerals may not dampen these effects.

Nature Climate Change↗

USGS2023

Natural climate solutions provide robust carbon mitigation capacity under future climate change scenarios

Natural climate solutions (NCS) are recognized as an important tool for governments to reduce greenhouse gas emissions and remove atmospheric carbon dioxide. Using California as a globally relevant reference, we evaluate the magnitude of biological climate mitigation potential from NCS starting in 2020 under four climate change scenarios. By mid-century NCS implementation leads to a large increase in net carbon stored, flipping the state from a net source to a net sink in two scenarios. Forest and conservation land management strategies make up 85% of all NCS emissions reductions by 2050, with agricultural strategies accounting for the remaining 15%. The most severe climate change impacts on ecosystem carbon materialize in the latter half of the century with three scenarios resulting in California ecosystems becoming a net source of carbon emissions under a baseline trajectory. However, NCS provide a strong attenuating effect, reducing land carbon emissions 41-54% by 2100 with total costs of deployment of 752–777 million USD annually through 2050. Rapid implementation of a portfolio of NCS interventions provides long-term investment in protecting ecosystem carbon in the face of climate change driven disturbances. This open-source, spatially-explicit framework can help evaluate risks to NCS carbon storage stability, implementation costs, and overall mitigation potential for NCS at jurisdictional scales.

California↗

USGS2002

The importance of rapid, disturbance-induced losses in carbon management and sequestration

Management of terrestrial carbon fluxes is being proposed as a means of increasing the amount of carbon sequestered in the terrestrial biosphere. This approach is generally viewed only as an interim strategy for the coming decades while other longer-term strategies are developed and implemented — the most important being the direct reduction of carbon emissions. We are concerned that the potential for rapid, disturbance-induced losses may be much greater than is currently appreciated, especially by the decision-making community. Here we wish to: (1) highlight the complex and threshold-like nature of disturbances — such as fire and drought, as well as the erosion associated with each — that could lead to carbon losses; (2) note the global extent of ecosystems that are at risk of such disturbance-induced carbon losses; and (3) call for increased consideration of and research on the mechanisms by which large, rapid disturbance-induced losses of terrestrial carbon could occur . Our lack of ability as a scientific community to predict such ecosystem dynamics is precluding the effective consideration of these processes into strategies and policies related to carbon management and sequestration. Consequently, scientists need to do more to improve quantification of these potential losses and to integrate them into sound, sustainable policy options.

Global Ecology and Biogeography↗

USGS2015

Ancient low–molecular-weight organic acids in permafrost fuel rapid carbon dioxide production upon thaw

Northern permafrost soils store a vast reservoir of carbon, nearly twice that of the present atmosphere. Current and projected climate warming threatens widespread thaw of these frozen, organic carbon (OC)-rich soils. Upon thaw, mobilized permafrost OC in dissolved and particulate forms can enter streams and rivers, which are important processors of OC and conduits for carbon dioxide (CO 2 ) to the atmosphere. Here, we demonstrate that ancient dissolved organic carbon (DOC) leached from 35,800 y B.P. permafrost soils is rapidly mineralized to CO 2 . During 200-h experiments in a novel high–temporal-resolution bioreactor, DOC concentration decreased by an average of 53%, fueling a more than sevenfold increase in dissolved inorganic carbon (DIC) concentration. Eighty-seven percent of the DOC loss to microbial uptake was derived from the low–molecular-weight (LMW) organic acids acetate and butyrate. To our knowledge, our study is the first to directly quantify high CO 2 production rates from permafrost-derived LMW DOC mineralization. The observed DOC loss rates are among the highest reported for permafrost carbon and demonstrate the potential importance of LMW DOC in driving the rapid metabolism of Pleistocene-age permafrost carbon upon thaw and the outgassing of CO 2 to the atmosphere by soils and nearby inland waters.

PNAS↗

USGS2018

Effects of contemporary land-use and land-cover change on the carbon balance of terrestrial ecosystems in the United States

Changes in land use and land cover (LULC) can have profound effects on terrestrial carbon dynamics, yet their effects on the global carbon budget remain uncertain. While land change impacts on ecosystem carbon dynamics have been the focus of numerous studies, few efforts have been based on observational data incorporating multiple ecosystem types spanning large geographic areas over long time horizons. In this study we use a variety of synoptic-scale remote sensing data to estimate the effect of LULC changes associated with urbanization, agricultural expansion and contraction, forest harvest, and wildfire on the carbon balance of terrestrial ecosystems (forest, grasslands, shrublands, and agriculture) in the conterminous United States (i.e. excluding Alaska and Hawaii) between 1973 and 2010. We estimate large net declines in the area of agriculture and forest, along with relatively small increases in grasslands and shrublands. The largest net change in any class was an estimated gain of 114 865 km 2 of developed lands, an average rate of 3282 km 2 yr −1 . On average, US ecosystems sequestered carbon at an annual rate of 254 Tg C yr −1 . In forest lands, the net sink declined by 35% over the study period, largely a result of land-use legacy, increasing disturbances, and reductions in forest area due to land use conversion. Uncertainty in LULC change data contributed to a ~16% margin of error in the annual carbon sink estimate prior to 1985 (approximately ±40 Tg C yr −1 ). Improvements in LULC and disturbance mapping starting in the mid-1980s reduced this uncertainty by ~50% after 1985. We conclude that changes in LULC are a critical component to understanding ecosystem carbon dynamics, and continued improvements in detection, quantification, and attribution of change have the potential to significantly reduce current uncertainties.

Environmental Research Letters↗

USGS2024

All tidal wetlands are blue carbon ecosystems

Managing coastal wetlands is one of the most promising activities to reduce atmospheric greenhouse gases, and it also contributes to meeting the United Nations Sustainable Development Goals. One of the options is through blue carbon projects, in which mangroves, saltmarshes, and seagrass are managed to increase carbon sequestration and reduce greenhouse gas emissions. However, other tidal wetlands align with the characteristics of blue carbon. These wetlands are called tidal freshwater wetlands in the United States, supratidal wetlands in Australia, transitional forests in Southeast Asia, and estuarine forests in South Africa. They have similar or larger potential for atmospheric carbon sequestration and emission reductions than the currently considered blue carbon ecosystems and have been highly exploited. In the present article, we suggest that all wetlands directly or indirectly influenced by tides should be considered blue carbon. Their protection and restoration through carbon offsets could reduce emissions while providing multiple cobenefits, including biodiversity.

BioScience↗

USGS2022

Deconstructing the microbial necromass continuum to inform soil carbon sequestration

Microbial necromass is a large, dynamic and persistent component of soil organic carbon, the dominant terrestrial carbon pool. Quantification of necromass carbon stocks and its susceptibility to global change is becoming standard practice in soil carbon research. However, the typical proxies used for necromass carbon do not reveal the dynamic nature of necromass carbon flows and transformations within soil that ultimately determine necromass persistence. In this review, we define and deconstruct four stages of the necromass continuum: production, recycling, stabilization and destabilization. Current understanding of necromass dynamics is described for each continuum stage. We highlight recent advances, methodological limitations and knowledge gaps which need to be addressed to determine necromass pool sizes and transformations. We discuss the dominant controls on necromass process rates and aspects of soil microscale structure including biofilms and food web interactions. The relative importance of each stage of the continuum is then compared in contrasting ecosystems and for climate change drivers. From the perspective of the continuum, we draw three conclusions to inform future research. First, controls on necromass persistence are more clearly defined when viewed through the lens of the continuum; second, destabilization is the least understood stage of the continuum with recycling also poorly evidenced outside of a few ecosystems; and third, the response of necromass process rates to climate change is unresolved for most continuum stages and ecosystems. Future mechanistic research focused on the role of biotic and abiotic soil microscale structure in determining necromass process rates and the relative importance of organo–mineral and organo–organo interactions can inform necromass persistence in different climate change scenarios. Our review demonstrates that deconstructing the necromass continuum is key to predicting the vulnerability and persistence of necromass carbon in a changing world.

Functional Ecology↗