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.

Explore Research Products in the PAR
It may take a few hours for recently added research products to appear in PAR search results.


Title: The Effects of Engineered Aeration on Atmospheric Methane Flux From a Chesapeake Bay Tidal Tributary
Engineered aeration is one solution for increasing oxygen concentrations in highly eutrophic estuaries that undergo seasonal hypoxia. Although there are various designs for engineered aeration, all approaches involve either destratification of the water column or direct injection of oxygen or air through fine bubble diffusion. To date, the effect of either approach on estuarine methane dynamics remains unknown. Here we tested the hypotheses that 1) bubble aeration will strip the water of methane and enhance the air-water methane flux to the atmosphere and 2) the addition of oxygen to the water column will enhance aerobic methane oxidation in the water column and potentially offset the air-water methane flux. These hypotheses were tested in Rock Creek, Maryland, a shallow-water sub-estuary to the Chesapeake Bay, using controlled, ecosystem-scale deoxygenation experiments where the water column and sediments were sampled in mid-summer, when aerators were ON, and then 1, 3, 7, and 13 days after the aerators were turned OFF. Experiments were performed under two system designs, large bubble and fine bubble approaches, using the same observational approach that combined discrete water sampling, long term water samplers (OsmoSamplers) and sediment porewater profiles. Regardless of aeration status, methane concentrations reached as high as 1,500 nmol L−1in the water column during the experiments and remained near 1,000 nmol L−1through the summer and into the fall. Since these concentrations are above atmospheric equilibrium of 3 nmol L−1, these data establish the sub-estuary as a source of methane to the atmosphere, with a maximum atmospheric flux as high as 1,500 µmol m−2d−1, which is comparable to fluxes estimated for other estuaries. Air-water methane fluxes were higher when the aerators were ON, over short time frames, supporting the hypothesis that aeration enhanced the atmospheric methane flux. The fine-bubble approach showed lower air-water methane fluxes compared to the larger bubble, destratification system. We found that the primary source of the methane was the sediments, however,in situmethane production or an upstream methane source could not be ruled out. Overall, our measurements of methane concentrations were consistently high in all times and locations, supporting consistent methane flux to the atmosphere.  more » « less
Award ID(s):
1756244
PAR ID:
10481358
Author(s) / Creator(s):
; ; ; ; ; ; ;
Publisher / Repository:
Frontiers in Environmental Science
Date Published:
Journal Name:
Frontiers in Environmental Science
Volume:
10
ISSN:
2296-665X
Format(s):
Medium: X
Sponsoring Org:
National Science Foundation
More Like this
  1. ; ; ; ; ; (, Journal of Geophysical Research: Biogeosciences)
    Abstract Coastal salt marshes store large amounts of carbon but the magnitude and patterns of greenhouse gas (GHG; i.e., carbon dioxide (CO2) and methane (CH4)) fluxes are unclear. Information about GHG fluxes from these ecosystems comes from studies of sediments or at the ecosystem‐scale (eddy covariance) but fluxes from tidal creeks are unknown. We measured GHG concentrations in water, water quality, meteorological parameters, sediment CO2efflux, ecosystem‐scale GHG fluxes, and plant phenology; all at half‐hour intervals over 1 year. Manual creek GHG flux measurements were used to calculate gas transfer velocity (k) and parameterize a model of water‐to‐atmosphere GHG fluxes. The creek was a source of GHGs to the atmosphere where tidal patterns controlled diel variability. Dissolved oxygen and wind speed were negatively correlated with creek CH4efflux. Despite lacking a seasonal pattern, creek CO2efflux was correlated with drivers such as turbidity across phenological phases. Overall, nighttime creek CO2efflux (3.6 ± 0.63 μmol/m2/s) was at least 2 times higher than nighttime marsh sediment CO2efflux (1.5 ± 1.23 μmol/m2/s). Creek CH4efflux (17.5 ± 6.9 nmol/m2/s) was 4 times lower than ecosystem‐scale CH4fluxes (68.1 ± 52.3 nmol/m2/s) across the year. These results suggest that tidal creeks are potential hotspots for CO2emissions and could contribute to lateral transport of CH4to the coastal ocean due to supersaturation of CH4(>6,000 μmol/mol) in water. This study provides insights for modeling GHG efflux from tidal creeks and suggests that changes in tide stage overshadow water temperature in determining magnitudes of fluxes. 
    more » « less
  2. ; ; ; (, Journal of Geophysical Research: Biogeosciences)
    Abstract Subterranean estuaries (STEs) form at the land‐sea boundary where groundwater and seawater mix. These biogeochemically reactive zones influence groundwater‐borne nutrient concentrations and speciation prior to export via submarine groundwater discharge (SGD). We examined a STE located along the York River Estuary (YRE) to determine if SGD delivers dissolved inorganic nitrogen (DIN) and phosphorus (DIP) to the overlying water. We assessed variations in STE geochemical profiles with depth across locations, times, and tidal stages, estimated N removal along the STE flow path, measured hydraulic gradients to estimate SGD, and calculated potential nutrient fluxes. Salinity, dissolved oxygen (DO), DIN, and DIP varied significantly with depth and season (p < 0.05), but not location or tidal stage. Ammonium dominated the DIN pool deep in the STE. Moving toward the sediment surface, ammonium concentrations decreased as nitrate and DO concentrations increased, suggesting nitrification. Potential sediment N removal rates mediated by denitrification were <8 mmoles N m−2 d−1. The total groundwater discharge rate was 38 ± 11 L m−2 d−1; discharge followed tidal and seasonal patterns. Net SGD nutrient fluxes were 0.065–3.2 and 0.019–0.093 mmoles m−2 d−1for DIN and DIP, respectively. However, microbial N removal in the STE may attenuate 0.58% to >100% of groundwater DIN. SGD fluxes were on the same order of magnitude as diffusive benthic fluxes but accounted for <10% of the nutrients delivered by fluvial advection in the YRE. Our results indicate the importance of STE biogeochemical transformations to SGD flux estimations and their role in coastal eutrophication and nutrient dynamics. 
    more » « less
  3. ; ; ; ; ; ; ; ; ; ; et al (, Global Biogeochemical Cycles)
    Abstract Processes controlling dissolved barium (dBa) were investigated along the GEOTRACES GA03 North Atlantic and GP16 Eastern Tropical Pacific transects, which traversed similar physical and biogeochemical provinces. Dissolved Ba concentrations are lowest in surface waters (∼35–50 nmol kg−1) and increase to 70–80 and 140–150 nmol kg−1in deep waters of the Atlantic and Pacific transects, respectively. Using water mass mixing models, we estimate conservative mixing that accounts for most of dBa variability in both transects. To examine nonconservative processes, particulate excess Ba (pBaxs) formation and dissolution rates were tracked by normalizing particulate excess230Th activities. Th‐normalized pBaxsfluxes, with barite as the likely phase, have subsurface maxima in the top 1,000 m (∼100–200 μmol m−2 year−1average) in both basins. Barite precipitation depletes dBa within oxygen minimum zones from concentrations predicted by water mass mixing, whereas inputs from continental margins, particle dissolution in the water column, and benthic diffusive flux raise dBa above predications. Average pBaxsburial efficiencies along GA03 and GP16 are ∼37% and 17%–100%, respectively, and do not seem to be predicated on barite saturation indices in the overlying water column. Using published values, we reevaluate the global freshwater dBa river input as 6.6 ± 3.9 Gmol year−1. Estuarine mixing processes may add another 3–13 Gmol year−1. Dissolved Ba inputs from broad shallow continental margins, previously unaccounted for in global marine summaries, are substantial (∼17 Gmol year−1), exceeding terrestrial freshwater inputs. Revising river and shelf dBa inputs may help bring the marine Ba isotope budget more into balance. 
    more » « less
  4. ; ; ; ; (, Journal of Geophysical Research: Biogeosciences)
    Abstract Tropical floodplains are an important source of methane (CH4) to the atmosphere, and ebullitive fluxes are likely to be important. We report direct measurements of CH4ebullition in common habitats on the Amazon floodplain over two years based on floating chambers that allowed detection of bubbles, and submerged bubble traps. Ebullition was highly variable in space and time. Of the 840 floating chamber measurements (equivalent to 8,690 min of 10‐min deployments), 22% captured bubbles. Ebullitive CH4fluxes, measured using bubble traps deployed for a total of approximately 230 days, ranged from 0 to 109 mmol CH4m−2 d−1, with a mean of 4.4 mmol CH4m−2 d−1. During falling water, a hydroacoustic echosounder detected bubbles in 24% of the 70‐m segments over 34 km. Ebullitive flux increased as the water level fell faster during falling water periods. In flooded forests, highest ebullitive fluxes occurred during falling water, while in open water and herbaceous plant habitats, higher ebullitive fluxes were measured during low water periods. The contribution of diffusive plus ebullitive CH4flux represented by ebullition varied from 1% (high and rising water in open water of the lake) to 93% (falling water in flooded forests) based on bubble traps. Combining ebullitive and diffusive fluxes among habitats in relation to variations in water depth and areal coverage of aquatic habitats provides the basis for improved floodplain‐wide estimates of CH4evasion. 
    more » « less
  5. ; ; ; ; ; ; ; ; ; ; et al (, Global Change Biology)
    Abstract Methane (CH4) is a potent greenhouse gas (GHG) with atmospheric concentrations that have nearly tripled since pre‐industrial times. Wetlands account for a large share of global CH4emissions, yet the magnitude and factors controlling CH4fluxes in tidal wetlands remain uncertain. We synthesized CH4flux data from 100 chamber and 9 eddy covariance (EC) sites across tidal marshes in the conterminous United States to assess controlling factors and improve predictions of CH4emissions. This effort included creating an open‐source database of chamber‐based GHG fluxes (https://doi.org/10.25573/serc.14227085). Annual fluxes across chamber and EC sites averaged 26 ± 53 g CH4m−2 year−1, with a median of 3.9 g CH4m−2 year−1, and only 25% of sites exceeding 18 g CH4m−2 year−1. The highest fluxes were observed at fresh‐oligohaline sites with daily maximum temperature normals (MATmax) above 25.6°C. These were followed by frequently inundated low and mid‐fresh‐oligohaline marshes with MATmax ≤25.6°C, and mesohaline sites with MATmax >19°C. Quantile regressions of paired chamber CH4flux and porewater biogeochemistry revealed that the 90th percentile of fluxes fell below 5 ± 3 nmol m−2 s−1at sulfate concentrations >4.7 ± 0.6 mM, porewater salinity >21 ± 2 psu, or surface water salinity >15 ± 3 psu. Across sites, salinity was the dominant predictor of annual CH4fluxes, while within sites, temperature, gross primary productivity (GPP), and tidal height controlled variability at diel and seasonal scales. At the diel scale, GPP preceded temperature in importance for predicting CH4flux changes, while the opposite was observed at the seasonal scale. Water levels influenced the timing and pathway of diel CH4fluxes, with pulsed releases of stored CH4at low to rising tide. This study provides data and methods to improve tidal marsh CH4emission estimates, support blue carbon assessments, and refine national and global GHG inventories. 
    more » « less
  • Citation Formats
  • MLA
  • APA
  • Chicago
  • BibTeX
  • Save / Share this Record
  • Send to Email