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Geology topics

Meredith A. Holgerson

Publications and source records attributed to Meredith A. Holgerson.

11 recordsLinked to original sources

Depth-resolved carbon dioxide and methane concentrations in 522 lakes, ponds, and reservoirs worldwide

Lakes, ponds, and reservoirs (hereafter: “lakes”) are important sources of the greenhouse gases carbon dioxide (CO 2 ) and methane (CH 4 ). Emissions of CO 2 and CH 4 from lakes are regulated in part by in-lake processes, including the production and storage of gases in the lower parts of the water column (bottom waters). However, while substantial efforts have been made to improve estimates of greenhouse gas emissions from lakes, limited data on gas concentrations along depth profiles have prevented the incorporation of bottom-water processes in global emission estimates. Here, we present GHG-depths: the largest existing dataset of depth-profile CO 2 and CH 4 measurements worldwide, including 522 lakes across 38 countries and all seven continents. These data include contributions from 45 research teams and 56 published studies, totaling 2558 discrete sampling events. As global change continues to alter biogeochemical cycling in lakes, these data can help improve mechanistic models to better predict greenhouse gas production and emission from lakes worldwide.

Scientific Data

Climate-smart wetlands can mitigate the wetland-methane feedback loop

Climate change is intensifying wetland methane emissions, reinforcing a feedback loop that accelerates warming and threatens wetlands’ role as natural climate solutions. We propose climate-smart interventions for wetland protection, restoration, and management that explicitly account for methane dynamics. Targeted interventions can weaken methane feedback while safeguarding ecological functions and services.

One Earth

Higher methanotroph abundance and bottom-water methane in ponds with floating photovoltaic arrays

Floating photovoltaic (FPV) arrays alter the methane (CH 4 ) cycling dynamics of waterbodies on which they are deployed. Here, we investigated dissolved CH 4 dynamics and associated CH 4 cycling microbial communities (methanogens and methanotrophs) in the second year of FPV deployment (70% aerial coverage) in experimental ponds. We found that bottom-water CH 4 concentrations were twice as high in ponds with FPV compared to those without, while surface water CH 4 concentrations were orders of magnitude lower than bottom-waters, but did not differ between treatments. There was no change in the relative abundances of putative sediment methanogens or methanotrophs, but FPV restructured methanogen communities. FPV promoted late-summer methanotroph blooms in the water column, with abundances surpassing 1,000,000 cells mL -1 . We conclude that prolonged periods of CH 4 production in low oxygen FPV ponds favored blooms of methanotrophs, that may mitigate diffusive CH 4 emissions to the atmosphere by consuming dissolved CH 4 .

BioRxiv

Global methane budget 2000-2020

Understanding and quantifying the global methane (CH 4 ) budget is important for assessing realistic pathways to mitigate climate change. CH 4 is the second most important human-influenced greenhouse gas in terms of climate forcing after carbon dioxide (CO 2 ), and both emissions and atmospheric concentrations of CH 4 have continued to increase since 2007 after a temporary pause. The relative importance of CH 4 emissions compared to those of CO 2 for temperature change is related to its shorter atmospheric lifetime, stronger radiative effect, and acceleration in atmospheric growth rate over the past decade, the causes of which are still debated. Two major challenges in quantifying the factors responsible for the observed atmospheric growth rate arise from diverse, geographically overlapping CH 4 sources and from the uncertain magnitude and temporal change in the destruction of CH 4 by short-lived and highly variable hydroxyl radicals (OH). To address these challenges, we have established a consortium of multidisciplinary scientists under the umbrella of the Global Carbon Project to improve, synthesise, and update the global CH 4 budget regularly and to stimulate new research on the methane cycle. Following Saunois et al. (2016, 2020), we present here the third version of the living review paper dedicated to the decadal CH 4 budget, integrating results of top-down CH 4 emission estimates (based on in situ and Greenhouse Gases Observing SATellite (GOSAT) atmospheric observations and an ensemble of atmospheric inverse-model results) and bottom-up estimates (based on process-based models for estimating land surface emissions and atmospheric chemistry, inventories of anthropogenic emissions, and data-driven extrapolations). We present a budget for the most recent 2010–2019 calendar decade (the latest period for which full data sets are available), for the previous decade of 2000–2009 and for the year 2020. The revision of the bottom-up budget in this 2025 edition benefits from important progress in estimating inland freshwater emissions, with better counting of emissions from lakes and ponds, reservoirs, and streams and rivers. This budget also reduces double counting across freshwater and wetland emissions and, for the first time, includes an estimate of the potential double counting that may exist (average of 23 Tg CH 4 yr −1 ). Bottom-up approaches show that the combined wetland and inland freshwater emissions average 248 [159–369] Tg CH 4 yr −1 for the 2010–2019 decade. Natural fluxes are perturbed by human activities through climate, eutrophication, and land use. In this budget, we also estimate, for the first time, this anthropogenic component contributing to wetland and inland freshwater emissions. Newly available gridded products also allowed us to derive an almost complete latitudinal and regional budget based on bottom-up approaches. For the 2010–2019 decade, global CH 4 emissions are estimated by atmospheric inversions (top-down) to be 575 Tg CH 4 yr −1 (range 553–586, corresponding to the minimum and maximum estimates of the model ensemble). Of this amount, 369 Tg CH 4 yr −1 or ∼ 65 % is attributed to direct anthropogenic sources in the fossil, agriculture, and waste and anthropogenic biomass burning (range 350–391 Tg CH 4 yr −1 or 63 %–68 %). For the 2000–2009 period, the atmospheric inversions give a slightly lower total emission than for 2010–2019, by 32 Tg CH 4 yr −1 (range 9–40). The 2020 emission rate is the highest of the period and reaches 608 Tg CH 4 yr −1 (range 581–627), which is 12 % higher than the average emissions in the 2000s. Since 2012, global direct anthropogenic CH 4 emission trends have been tracking scenarios that assume no or minimal climate mitigation policies proposed by the Intergovernmental Panel on Climate Change (shared socio-economic pathways SSP5 and SSP3). Bottom-up methods suggest 16 % (94 Tg CH 4 yr −1 ) larger global emissions (669 Tg CH 4 yr −1 , range 512–849) than top-down inversion methods for the 2010–2019 period. The discrepancy between the bottom-up and the top-down budgets has been greatly reduced compared to the previous differences (167 and 156 Tg CH 4 yr −1 in Saunois et al. (2016, 2020) respectively), and for the first time uncertainties in bottom-up and top-down budgets overlap. Although differences have been reduced between inversions and bottom-up, the most important source of uncertainty in the global CH 4 budget is still attributable to natural emissions, especially those from wetlands and inland freshwaters. The tropospheric loss of methane, as the main contributor to methane lifetime, has been estimated at 563 [510–663] Tg CH 4 yr −1 based on chemistry–climate models. These values are slightly larger than for 2000–2009 due to the impact of the rise in atmospheric methane and remaining large uncertainty ( ∼ 25 %). The total sink of CH 4 is estimated at 633 [507–796] Tg CH 4 yr −1 by the bottom-up approaches and at 554 [550–567] Tg CH 4 yr −1 by top-down approaches. However, most of the top-down models use the same OH distribution, which introduces less uncertainty to the global budget than is likely justified. For 2010–2019, agriculture and waste contributed an estimated 228 [213–242] Tg CH 4 yr −1 in the top-down budget and 211 [195–231] Tg CH 4 yr −1 in the bottom-up budget. Fossil fuel emissions contributed 115 [100–124] Tg CH 4 yr −1 in the top-down budget and 120 [117–125] Tg CH 4 yr −1 in the bottom-up budget. Biomass and biofuel burning contributed 27 [26–27] Tg CH 4 yr −1 in the top-down budget and 28 [21–39] Tg CH 4 yr −1 in the bottom-up budget. We identify five major priorities for improving the CH 4 budget: (i) producing a global, high-resolution map of water-saturated soils and inundated areas emitting CH 4 based on a robust classification of different types of emitting ecosystems; (ii) further development of process-based models for inland-water emissions; (iii) intensification of CH 4 observations at local (e.g. FLUXNET-CH 4 measurements, urban-scale monitoring, satellite imagery with pointing capabilities) to regional scales (surface networks and global remote sensing measurements from satellites) to constrain both bottom-up models and atmospheric inversions; (iv) improvements of transport models and the representation of photochemical sinks in top-down inversions; and (v) integration of 3D variational inversion systems using isotopic and/or co-emitted species such as ethane as well as information in the bottom-up inventories on anthropogenic super-emitters detected by remote sensing (mainly oil and gas sector but also coal, agriculture, and landfills) to improve source partitioning.

Earth System Science Data

Immediate effect of floating solar energy deployment on greenhouse gas dynamics in ponds

Floating photovoltaic (FPV) solar energy offers promise for renewable electricity production that spares land for other societal benefits. FPV deployment may alter greenhouse gas (GHG) production and emissions from waterbodies by changing physical, chemical, and biological processes, which can have implications for the carbon cost of energy production with FPV. Here, we use an ecosystem-scale experiment to assess how GHG dynamics in ponds respond to installation of operationally representative FPV. Following FPV deployments of 70% array coverage, daily whole-pond GHG emissions increased by 26.8% on a carbon dioxide-equivalent (CO 2 -eq) basis, and dissolved oxygen availability rapidly decreased. Despite increased emissions following FPV deployment, FPV-derived GHG emissions from waterbodies are likely lower than landscape GHG emissions associated with terrestrial solar and hydropower production on a CO 2 -eq kWh –1 basis. Adaptive management strategies like bubbler installation may reduce the magnitude of FPV impacts on GHG and dissolved oxygen dynamics.

Environmental Science and Technology

Submersed macrophyte density regulates aquatic greenhouse gas emissions

Shallow freshwater ecosystems emit large amounts of greenhouse gases (GHGs), such as carbon dioxide (CO 2 ) and methane (CH 4 ), yet emissions are highly variable. The role that aquatic macrophytes play in regulating aquatic GHG emissions is uncertain despite their ability to dominate shallow waterbodies. Here, we studied the effects of submersed macrophyte ( Ceratophyllum demersum ) density on CO 2 and CH 4 concentrations and fluxes. We conducted a 61-days experiment using mesocosms containing one of the following C . demersum density treatments: 0, 10, 20, or 30 individual shoots ( n = 3). We found that high density C . demersum had the highest CO 2 and CH 4 surface water concentrations and emissions while there was no significant difference in CH 4 in the low and medium densities and no plant control. The high density treatment lost biomass over the course of the experiment, indicating die-off and additions of organic matter to the sediment. High organic matter loading and low dissolved oxygen likely stimulated GHG production in the high density treatment. Our results emphasize that submersed macrophyte density and periods of growth and dieback are important in regulating GHG emissions, which may help explain why shallow waterbodies are high yet variable sources of GHGs to the atmosphere.

JGR Biogeosciences

Inland water greenhouse gas budgets for RECCAP2: 2. Regionalization and homogenization of estimates

Inland waters are important sources of the greenhouse gasses (GHGs) carbon dioxide (CO 2 ), methane (CH 4 ) and nitrous oxide (N 2 O) to the atmosphere. In the framework of the 2 nd phase of the REgional Carbon Cycle Assessment and Processes (RECCAP-2) initiative, we synthesize existing estimates of GHG emissions from streams, rivers, lakes and reservoirs, and homogenize them with regard to underlying global maps of water surface area distribution and the effects of seasonal ice cover. We then produce regionalized estimates of GHG emissions over 10 extensive land regions. According to our synthesis, inland water GHG emissions have a global warming potential of an equivalent emission of 13.5 (9.9-20.1) and 8.3 (5.7-12.7) Pg CO 2 -eq. yr -1 at a 20 and 100 year horizon (GWP 20 and GWP 100 ), respectively. Contributions of CO 2 dominate GWP 100 , with rivers being the largest emitter. For GWP 20 , lakes and rivers are equally important emitters, and the warming potential of CH 4 is more important than that of CO 2 . Contributions from N 2 O are about two orders of magnitude lower. Normalized to the area of RECCAP-2 regions, S-America and SE-Asia show the highest emission rates, dominated by riverine CO 2 emissions.

Global Biogeochemical Cycles

Inland water greenhouse gas budgets for RECCAP2: 1. State-of-the-art of global scale assessments

Inland waters are important sources of the greenhouse gasses (GHGs) carbon dioxide (CO 2 ), methane (CH 4 ) and nitrous oxide (N 2 O) to the atmosphere. In the framework of the 2 nd phase of the REgional Carbon Cycle Assessment and Processes (RECCAP-2) initiative, we review the state of the art in estimating inland water GHG budgets at global scale, which has substantially advanced since the first phase of RECCAP nearly ten years ago. The development of increasingly sophisticated upscaling techniques, including statistical prediction and process based models, allows for spatially explicit estimates which are needed for regionalized assessments of continental GHG budgets such as those established for RECCAP. A few recent estimates also resolve the seasonal and/or interannual variability in inland water GHG emissions. Nonetheless, the global-scale assessment of inland water emissions remains challenging because of limited spatial and temporal coverage of observations and persisting uncertainties in the abundance and distribution of inland water surface areas. To decrease these uncertainties, more empirical work on the contributions of hot-spots and hot-moments to overall inland water GHG emissions is particularly needed.

Global Biogeochemical Cycles

Integrating ecosystem metabolism and consumer allochthony reveals nonlinear drivers in lake organic matter processing

Lakes process both terrestrial and aquatic organic matter, and the relative contribution from each source is often measured via ecosystem metabolism and terrestrial resource use in the food web (i.e., consumer allochthony). Yet, ecosystem metabolism and consumer allochthony are rarely considered together, despite possible interactions and potential for them to respond to the same lake characteristics. In this study, we compiled global datasets of lake gross primary production (GPP), ecosystem respiration (ER), and zooplankton allochthony to compare the strength and shape of relationships with physicochemical characteristics across a broad set of lakes. GPP was positively related to total phosphorus (TP) in lakes with intermediate TP concentrations (11–75 μ g L −1 ) and was highest in lakes with intermediate dissolved organic carbon (DOC) concentrations. While ER and GPP were strongly positively correlated, decoupling occurred at high DOC concentrations. Lastly, allochthony had a unimodal relationship with TP and related variably to DOC. By integrating metabolism and allochthony, we identified similar change points in GPP and zooplankton allochthony at intermediate DOC (4.5–10 mg L −1 ) and TP (8–20 μ g L −1 ) concentrations, indicating that allochthony and GPP may be coupled and inversely related. The ratio of DOC:nutrients also helped to identify conditions where lake organic matter processing responded more to autochthonous or allochthonous organic matter sources. As lakes globally face eutrophication and browning, predicting how lake organic matter processing will respond requires an updated paradigm that incorporates nonlinear dynamics and interactions.

Limnology and Oceanography

Drivers of methane flux differ between lakes and reservoirs, complicating global upscaling efforts

Methane is an important greenhouse gas with growing atmospheric concentrations. Freshwater lakes and reservoirs contribute substantially to atmospheric methane concentrations, but the magnitude of this contribution is poorly constrained. Uncertainty stems partially from whether the sites currently sampled represent the global population as well as incomplete knowledge of which environmental variables predict methane flux. Thus, determining the main drivers of methane flux across diverse waterbody types will inform more accurate upscaling approaches. Here we use a new database of total, diffusive, and ebullitive areal methane emissions from 313 lakes and reservoirs (ranging in surface area from 6 m 2 to 5,400 km 2 ) to identify the best predictors of methane emission. We found that the best predictors of methane emission differed by waterbody type (lakes vs. reservoirs), and that ecosystem morphometric variables (e.g., surface area and maximum depth) were more important predictors in lakes whereas metrics of autochthonous production (e.g., chlorophyll a ) were more important in reservoirs. We also found that productivity strongly predicted methane ebullition, whereas ecosystem morphometry and waterbody type were more important predictors of diffusive methane flux. Finally, we identify several knowledge gaps that limit upscaling efforts. First, we need more methane emission measurements in small reservoirs, large lakes, and both natural and artificial ponds. Additionally, more accurate upscaling efforts require improved global information about waterbody surface area, waterbody type (lake vs. reservoir), ice phenology, and the distribution of productivity‐related predictor variables such as total phosphorus, DOC, and chlorophyll a .

Journal of Geophysical Research-Biogeosciences

Half of global methane emissions come from highly variable aquatic ecosystem sources

Atmospheric methane is a potent greenhouse gas that plays a major role in controlling the Earth’s climate. The causes of the renewed increase of methane concentration since 2007 are uncertain given the multiple sources and complex biogeochemistry. Here, we present a metadata analysis of methane fluxes from all major natural, impacted and human-made aquatic ecosystems. Our revised bottom-up global aquatic methane emissions combine diffusive, ebullitive and/or plant-mediated fluxes from 15 aquatic ecosystems. We emphasize the high variability of methane fluxes within and between aquatic ecosystems and a positively skewed distribution of empirical data, making global estimates sensitive to statistical assumptions and sampling design. We find aquatic ecosystems contribute (median) 41% or (mean) 53% of total global methane emissions from anthropogenic and natural sources. We show that methane emissions increase from natural to impacted aquatic ecosystems and from coastal to freshwater ecosystems. We argue that aquatic emissions will probably increase due to urbanization, eutrophication and positive climate feedbacks and suggest changes in land-use management as potential mitigation strategies to reduce aquatic methane emissions.

Nature Geoscience