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.

Attention:

The NSF Public Access Repository (PAR) system and access will be unavailable from 10:00 PM ET on Friday, February 6 until 10:00 AM ET on Saturday, February 7 due to maintenance. We apologize for the inconvenience.


Title: Characterizing Performance of Freshwater Wetland Methane Models Across Time Scales at FLUXNET‐CH 4 Sites Using Wavelet Analyses
Abstract Process‐based land surface models are important tools for estimating global wetland methane (CH4) emissions and projecting their behavior across space and time. So far there are no performance assessments of model responses to drivers at multiple time scales. In this study, we apply wavelet analysis to identify the dominant time scales contributing to model uncertainty in the frequency domain. We evaluate seven wetland models at 23 eddy covariance tower sites. Our study first characterizes site‐level patterns of freshwater wetland CH4fluxes (FCH4) at different time scales. A Monte Carlo approach was developed to incorporate flux observation error to avoid misidentification of the time scales that dominate model error. Our results suggest that (a) significant model‐observation disagreements are mainly at multi‐day time scales (<15 days); (b) most of the models can capture the CH4variability at monthly and seasonal time scales (>32 days) for the boreal and Arctic tundra wetland sites but have significant bias in variability at seasonal time scales for temperate and tropical/subtropical sites; (c) model errors exhibit increasing power spectrum as time scale increases, indicating that biases at time scales <5 days could contribute to persistent systematic biases on longer time scales; and (d) differences in error pattern are related to model structure (e.g., proxy of CH4production). Our evaluation suggests the need to accurately replicate FCH4variability, especially at short time scales, in future wetland CH4model developments.  more » « less
Award ID(s):
1652594
PAR ID:
10490764
Author(s) / Creator(s):
; ; ; ; ; ; ; ; ; ; ; ; ; ; ; ; ; ; ; more » ; ; ; ; ; ; ; ; ; « less
Publisher / Repository:
Wiley
Date Published:
Journal Name:
Journal of Geophysical Research: Biogeosciences
Volume:
128
Issue:
11
ISSN:
2169-8953
Format(s):
Medium: X
Sponsoring Org:
National Science Foundation
More Like this
  1. Abstract Wetlands are responsible for 20%–31% of global methane (CH4) emissions and account for a large source of uncertainty in the global CH4budget. Data‐driven upscaling of CH4fluxes from eddy covariance measurements can provide new and independent bottom‐up estimates of wetland CH4emissions. Here, we develop a six‐predictor random forest upscaling model (UpCH4), trained on 119 site‐years of eddy covariance CH4flux data from 43 freshwater wetland sites in the FLUXNET‐CH4 Community Product. Network patterns in site‐level annual means and mean seasonal cycles of CH4fluxes were reproduced accurately in tundra, boreal, and temperate regions (Nash‐Sutcliffe Efficiency ∼0.52–0.63 and 0.53). UpCH4 estimated annual global wetland CH4emissions of 146 ± 43 TgCH4 y−1for 2001–2018 which agrees closely with current bottom‐up land surface models (102–181 TgCH4 y−1) and overlaps with top‐down atmospheric inversion models (155–200 TgCH4 y−1). However, UpCH4 diverged from both types of models in the spatial pattern and seasonal dynamics of tropical wetland emissions. We conclude that upscaling of eddy covariance CH4fluxes has the potential to produce realistic extra‐tropical wetland CH4emissions estimates which will improve with more flux data. To reduce uncertainty in upscaled estimates, researchers could prioritize new wetland flux sites along humid‐to‐arid tropical climate gradients, from major rainforest basins (Congo, Amazon, and SE Asia), into monsoon (Bangladesh and India) and savannah regions (African Sahel) and be paired with improved knowledge of wetland extent seasonal dynamics in these regions. The monthly wetland methane products gridded at 0.25° from UpCH4 are available via ORNL DAAC (https://doi.org/10.3334/ORNLDAAC/2253). 
    more » « less
  2. Abstract Headwater wetlands are important sites for carbon storage and emissions. While local- and landscape-scale factors are known to influence wetland carbon biogeochemistry, the spatial and temporal heterogeneity of these factors limits our predictive understanding of wetland carbon dynamics. To address this issue, we examined relationships between carbon dioxide (CO2) and methane (CH4) concentrations with wetland hydrogeomorphology, water level, and biogeochemical conditions. We sampled water chemistry and dissolved gases (CO2and CH4) and monitored continuous water level at 20 wetlands and co-located upland wells in the Delmarva Peninsula, Maryland, every 1–3 months for 2 years. We also obtained wetland hydrogeomorphologic metrics at maximum inundation (area, perimeter, and volume). Wetlands in our study were supersaturated with CO2(mean = 315 μM) and CH4(mean = 15 μM), highlighting their potential role as carbon sources to the atmosphere. Spatial and temporal variability in CO2and CH4concentrations was high, particularly for CH4, and both gases were more spatially variable than temporally. We found that groundwater is a potential source of CO2in wetlands and CO2decreases with increased water level. In contrast, CH4concentrations appear to be related to substrate and nutrient availability and to drying patterns over a longer temporal scale. At the landscape scale, wetlands with higher perimeter:area ratios and wetlands with higher height above the nearest drainage had higher CO2and CH4concentrations. Understanding the variability of CO2and CH4in wetlands, and how these might change with changing environmental conditions and across different wetland types, is critical to understanding the current and future role of wetlands in the global carbon cycle. 
    more » « less
  3. This paper describes the formation of, and initial results for, a new FLUXNET coordination network for ecosystem-scale methane (CH 4 ) measurements at 60 sites globally, organized by the Global Carbon Project in partnership with other initiatives and regional flux tower networks. The objectives of the effort are presented along with an overview of the coverage of eddy covariance (EC) CH 4 flux measurements globally, initial results comparing CH 4 fluxes across the sites, and future research directions and needs. Annual estimates of net CH 4 fluxes across sites ranged from −0.2 ± 0.02 g C m –2 yr –1 for an upland forest site to 114.9 ± 13.4 g C m –2 yr –1 for an estuarine freshwater marsh, with fluxes exceeding 40 g C m –2 yr –1 at multiple sites. Average annual soil and air temperatures were found to be the strongest predictor of annual CH 4 flux across wetland sites globally. Water table position was positively correlated with annual CH 4 emissions, although only for wetland sites that were not consistently inundated throughout the year. The ratio of annual CH 4 fluxes to ecosystem respiration increased significantly with mean site temperature. Uncertainties in annual CH 4 estimates due to gap-filling and random errors were on average ±1.6 g C m –2 yr –1 at 95% confidence, with the relative error decreasing exponentially with increasing flux magnitude across sites. Through the analysis and synthesis of a growing EC CH 4 flux database, the controls on ecosystem CH 4 fluxes can be better understood, used to inform and validate Earth system models, and reconcile differences between land surface model- and atmospheric-based estimates of CH 4 emissions. 
    more » « less
  4. Abstract Methane (CH4) emissions from wetland ecosystems are controlled by redox conditions in the soil, which are currently underrepresented in Earth system models. Plant-mediated radial oxygen loss (ROL) can increase soil O2availability, affect local redox conditions, and cause heterogeneous distribution of redox-sensitive chemical species at the root scale, which would affect CH4emissions integrated over larger scales. In this study, we used a subsurface geochemical simulator (PFLOTRAN) to quantify the effects of incorporating either spatially homogeneous ROL or more complex heterogeneous ROL on model predictions of porewater solute concentration depth profiles (dissolved organic carbon, methane, sulfate, sulfide) and column integrated CH4fluxes for a tidal coastal wetland. From the heterogeneous ROL simulation, we obtained 18% higher column averaged CH4concentration at the rooting zone but 5% lower total CH4flux compared to simulations of the homogeneous ROL or without ROL. This difference is because lower CH4concentrations occurred in the same rhizosphere volume that was directly connected with plant-mediated transport of CH4from the rooting zone to the atmosphere. Sensitivity analysis indicated that the impacts of heterogeneous ROL on model predictions of porewater oxygen and sulfide concentrations will be more important under conditions of higher ROL fluxes or more heterogeneous root distribution (lower root densities). Despite the small impact on predicted CH4emissions, the simulated ROL drastically reduced porewater concentrations of sulfide, an effective phytotoxin, indicating that incorporating ROL combined with sulfur cycling into ecosystem models could potentially improve predictions of plant productivity in coastal wetland ecosystems. 
    more » « less
  5. 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