skip to main content
US FlagAn official website of the United States government
dot gov icon
Official websites use .gov
A .gov website belongs to an official government organization in the United States.
https lock icon
Secure .gov websites use HTTPS
A lock ( lock ) or https:// means you've safely connected to the .gov website. Share sensitive information only on official, secure websites.


Title: Waterfalls enhance regional methane emissions by enabling dissolved methane to bypass microbial oxidation
River waters are significant sources of atmospheric methane whose local emissions increase with river slope and turbulence. However, when integrated regionally, the amount of dissolved methane released to the atmosphere is uninfluenced by local changes in turbulence when no additional loss mechanisms are present. Here we tested the hypothesis that waterfalls enhance both local and regional atmospheric methane emissions if microbial methane oxidation is significant in river waters. Rates of net atmospheric emission and net aerobic methane oxidation were measured in river waters containing waterfalls across western New York revealing that methane oxidation can diminish atmospheric emissions when turbulence is less. However, at waterfalls, 88 ± 1% of the dissolved methane supersaturation was released to the atmosphere, increasing net methane emission rates substantially beyond oxidation (0.1–16.2 × 10^6 nM d^-1 for waterfall emission; 10–39 nM d^-1 for oxidation), and ultimately enhancing regional methane emissions by enabling dissolved methane to bypass an oxidative sink.  more » « less
Award ID(s):
2241873 2023514 1634871
PAR ID:
10576322
Author(s) / Creator(s):
; ;
Publisher / Repository:
Springer Nature
Date Published:
Journal Name:
Communications Earth & Environment
Volume:
6
Issue:
1
ISSN:
2662-4435
Format(s):
Medium: X
Sponsoring Org:
National Science Foundation
More Like this
  1. Inland waters are the largest natural source of methane (CH 4 ) to the atmosphere, yet the contribution from small streams to this flux is not clearly defined. To fully understand CH 4 emissions from streams and rivers, we must consider the relative importance of CH 4 emission pathways, the prominence of microbially-mediated production and oxidation of CH 4 , and the isotopic signature of emitted CH 4 . Here, we construct a complete CH 4 emission budgets for four lowland headwater streams by quantifying diffusive CH 4 emissions and comparing them to previously published rates of ebullitive emissions. We also examine the isotopic composition of CH 4 along with the sediment microbial community to investigate production and oxidation across the streams. We find that all four streams are supersaturated with respect to CH 4 with diffusive emissions accounting for approximately 78–100% of total CH 4 emissions. Isotopic and microbial data suggest CH 4 oxidation is prevalent across the streams, depleting approximately half of the dissolved CH 4 pool before emission. We propose a conceptual model of CH 4 production, oxidation, and emission from small streams, where the dominance of diffusive emissions is greater compared to other aquatic ecosystems, and the impact of CH 4 oxidation is observable in the emitted isotopic values. As a result, we suggest the CH 4 emitted from small streams is isotopically heavy compared to lentic ecosystems. Our results further demonstrate streams are important components of the global CH 4 cycle yet may be characterized by a unique pattern of cycling and emission that differentiate them from other aquatic ecosystems. 
    more » « less
  2. Abstract Floodplains lakes are abundant in the Amazon basin and are important methane sources to the atmosphere. Existing biogeochemical models require modifications and inclusion of hydrodynamic processes operative in shallow, warm waters to be applied to these aquatic ecosystems. We modified a 1‐dimensional process‐based, lake biogeochemical model and combined a 3‐dimensional hydrodynamic model to suit Amazon floodplains. We evaluated the combined model's performance simulating methane concentrations and fluxes and several related processes in the open lake and an embayment of a well‐studied Amazon lake. Parameters for calibration were selected through sensitivity tests using a machine learning‐based algorithm, classification, and regression trees. Comparison between simulated and measured fluxes indicate generally good agreement in seasonal patterns and magnitudes. Comparisons of near‐surface concentrations varied with no clear patterns. Simulations of methane concentrations at near‐surface and near‐bottom, and diffusive emissions are most sensitive to carbon mineralization rate, Q10factors for methanogenesis and oxidation, and methane oxidation potential. Modeled rates of planktonic photosynthesis were generally lower than measurements, though simulated planktonic respiration was often similar to measurements. Simulated rates of methane oxidation were considerably lower, with a few exceptions, than measurements of methane oxidation in oxic water of the lake. Improvements of results of the linked hydrodynamic‐biogeochemical model will result from inclusion of advective transport, use of parameter values appropriate for tropical waters, especially for methane oxidation and photosynthesis, and addition of changes in hydrostatic pressure to model of ebullition. 
    more » « less
  3. Abstract Tropical wetlands and freshwaters are major contributors to the growing atmospheric methane (CH4) burden. Extensive peatland drainage has lowered CH4emissions from peat soils in Southeast Asia, but the canals draining these peatlands may be hotspots of CH4emissions. Alternatively, CH4oxidation (consumption) by methanotrophic microorganisms may attenuate emissions. Here, we used laboratory experiments and a synoptic survey of the isotopic composition of CH4in 34 canals across West Kalimantan, Indonesia to quantify the proportion of CH4that is consumed and therefore not emitted to the atmosphere. We find that CH4oxidation mitigates 76.4 ± 12.0% of potential canal emissions, reducing emissions by ~70 mg CH4m−2d−1. Methane consumption also significantly impacts the stable isotopic fingerprint of canal CH4emissions. As canals drain over 65% of peatlands in Southeast Asia, our results suggest that CH4oxidation significantly influences landscape-scale CH4emissions from these ecosystems. 
    more » « less
  4. NA (Ed.)
    Abstract. Reducing methane emissions from the oil and gas (oil–gas) sector has been identified as a critically important global strategy for reducing near-term climate warming. Recent measurements, especially by satellite and aerial remote sensing, underscore the importance of targeting the small number of facilities emitting methane at high rates (i.e., “super-emitters”) for measurement and mitigation. However, the contributions from individual oil–gas facilities emitting at low emission rates that are often undetected are poorly understood, especially in the context of total national- and regional-level estimates. In this work, we compile empirical measurements gathered using methods with low limits of detection to develop facility-level estimates of total methane emissions from the continental United States (CONUS) midstream and upstream oil–gas sector for 2021. We find that of the total 14.6 (12.7–16.8) Tg yr−1 oil–gas methane emissions in the CONUS for the year 2021, 70 % (95 % confidence intervals: 61 %–81 %) originate from facilities emitting <100kgh-1 and 30 % (26 %–34 %) and ∼80 % (68 %–90 %) originate from facilities emitting <10 and <200kgh-1, respectively. While there is variability among the emission distribution curves for different oil–gas production basins, facilities with low emissions are consistently found to account for the majority of total basin emissions (i.e., range of 60 %–86 % of total basin emissions from facilities emitting <100kgh-1). We estimate that production well sites were responsible for 70 % of regional oil–gas methane emissions, from which we find that the well sites that accounted for only 10 % of national oil and gas production in 2021 disproportionately accounted for 67 %–90 % of the total well site emissions. Our results are also in broad agreement with data obtained from several independent aerial remote sensing campaigns (e.g., MethaneAIR, Bridger Gas Mapping LiDAR, AVIRIS-NG (Airborne Visible/Infrared Imaging System – Next Generation), and Global Airborne Observatory) across five to eight major oil–gas basins. Our findings highlight the importance of accounting for the significant contribution of small emission sources to total oil–gas methane emissions. While reducing emissions from high-emitting facilities is important, it is not sufficient for the overall mitigation of methane emissions from the oil and gas sector which according to this study is dominated by small emission sources across the US. Tracking changes in emissions over time and designing effective mitigation policies should consider the large contribution of small methane sources to total emissions. 
    more » « less
  5. Abstract Soils are a major source of nitrogen oxides, which in the atmosphere help govern its oxidative capacity. Thus the response of soil nitric oxide (NO) emissions to forcings such as warming or forest loss has a meaningful impact on global atmospheric chemistry. We find that the soil emission rate of NO in Amazonia from a common inventory is biased low by at least an order of magnitude in comparison to tower‐based observations. Accounting for this regional bias decreases the modeled global methane lifetime by 1.4%–2.6%. In comparison, a fully deforested Amazonia, representing a 37% decrease in global emissions of isoprene, decreases methane lifetime by at most 4.6%, highlighting the sensitive response of oxidation rates to changes in emissions of NO compared to those of terpenes. Our results demonstrate that improving our understanding of soil NO emissions will yield a more accurate representation of atmospheric oxidative capacity. 
    more » « less