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: Post-fire soil emissions of nitric oxide (NO) and nitrous oxide (N2O) across global ecosystems: a review
Abstract Wildfires may increase soil emissions of trace nitrogen (N) gases like nitric oxide (NO) and nitrous oxide (N2O) by changing soil physicochemical conditions and altering microbial processes like nitrification and denitrification. When 34 studies were synthesized, we found a significant increase in both NO and N2O emissions up to 1 year post-fire across studies spanning ecosystems globally. However, when fluxes were separated by ecosystem type, we found that individual ecosystem types responded uniquely to fire. Forest soils tended to emit more N2O after fire, but there was no significant effect on NO. Shrubland soils showed significant increases in both NO and N2O emissions after fires; often with extremely large but short-lived NO pulses occurring immediately after fire. Grassland NO emissions increased after fire, but the size of this effect was small relative to shrublands. N2O emissions from burned grasslands were highly variable with no significant effect. To better understand the variation in responses to fire across global ecosystems, more consistent measurements of variables recognized as important controls on soil fluxes of NO and N2O (e.g., N cycling rates, soil water content, pH, and substrate availability) are needed across studies. We also suggest that fire-specific elements like burn severity, microbial community succession, and the presence of char be considered by future studies. Our synthesis suggests that fires can exacerbate ecosystem N loss long after they burn, increasing soil emissions of NO and N2O with implications for ecosystem N loss, climate, and regional air quality as wildfires increase globally.  more » « less
Award ID(s):
1916622
PAR ID:
10461064
Author(s) / Creator(s):
;
Publisher / Repository:
Springer Science + Business Media
Date Published:
Journal Name:
Biogeochemistry
Volume:
165
Issue:
3
ISSN:
0168-2563
Format(s):
Medium: X Size: p. 291-309
Size(s):
p. 291-309
Sponsoring Org:
National Science Foundation
More Like this
  1. Abstract In seasonally dry ecosystems, which are common in sub‐Saharan Africa, precipitation after dry periods can cause large pulses of nitrous oxide (N2O), a greenhouse gas, and of nitric oxide (NO), a precursor to tropospheric ozone pollution. Agricultural practices can change soil characteristics, affecting trace N gas emissions. To evaluate the effects of land use on trace gas pulses at the start of the rainy season, we conducted laboratory measurements of N2O and NO fluxes from soils collected from four pairs of agricultural and natural savannah sites across the Sudano‐Sahelian zone. We also conducted in situ wetting experiments, measuring NO fluxes from fallow sandy soils in Tanzania and NO and N2O fluxes from clayey soils in Kenya with different histories of fertilizer use. In incubation studies, NO increased by a factor of 7 to 25 following wetting, and N2O fluxes shifted from negative to positive; cumulative NO fluxes were an order of magnitude larger than cumulative N2O fluxes. In Kenya and Tanzania, NO increased by 1 to 2 orders of magnitude after wetting, and N2O increased by a factor of roughly 5 to 10. Cumulative NO fluxes ranged from 87 to 115 g NO‐N ha−1across both countries—a substantial proportion of annual emissions—compared to roughly 1 g N2O‐N in Kenya. There were no effects of land use or fertilization history on the magnitude of NO or N2O pulses, though land use may have been confounded with differences in soil texture potentially limiting the ability to detect land use effects. 
    more » « less
  2. null (Ed.)
    Abstract Wildfires are a major disturbance to forest carbon (C) balance through both immediate combustion emissions and post-fire ecosystem dynamics. Here we used a process-based biogeochemistry model, the Terrestrial Ecosystem Model (TEM), to simulate C budget in Alaska and Canada during 1986–2016, as impacted by fire disturbances. We extracted the data of difference Normalized Burn Ratio (dNBR) for fires from Landsat TM/ETM imagery and estimated the proportion of vegetation and soil C combustion. We observed that the region was a C source of 2.74 Pg C during the 31-year period. The observed C loss, 57.1 Tg C year −1 , was attributed to fire emissions, overwhelming the net ecosystem production (1.9 Tg C year −1 ) in the region. Our simulated direct emissions for Alaska and Canada are within the range of field measurements and other model estimates. As burn severity increased, combustion emission tended to switch from vegetation origin towards soil origin. When dNBR is below 300, fires increase soil temperature and decrease soil moisture and thus, enhance soil respiration. However, the post-fire soil respiration decreases for moderate or high burn severity. The proportion of post-fire soil emission in total emissions increased with burn severity. Net nitrogen mineralization gradually recovered after fire, enhancing net primary production. Net ecosystem production recovered fast under higher burn severities. The impact of fire disturbance on the C balance of northern ecosystems and the associated uncertainties can be better characterized with long-term, prior-, during- and post-disturbance data across the geospatial spectrum. Our findings suggest that the regional source of carbon to the atmosphere will persist if the observed forest wildfire occurrence and severity continues into the future. 
    more » « less
  3. Abstract The atmospheric concentration of nitrous oxide (N2O) has increased by 23% since the pre‐industrial era, which substantially destructed the stratospheric ozone layer and changed the global climate. However, it remains uncertain about the reasons behind the increase and the spatiotemporal patterns of soil N2O emissions, a primary biogenic source. Here, we used an integrative land ecosystem model, Dynamic Land Ecosystem Model (DLEM), to quantify direct (i.e., emitted from local soil) and indirect (i.e., emissions related to local practices but occurring elsewhere) N2O emissions in the contiguous United States during 1900–2019. Newly developed geospatial data of land‐use history and crop‐specific agricultural management practices were used to force DLEM at a spatial resolution of 5 arc‐min by 5 arc‐min. The model simulation indicates that the U.S. soil N2O emissions totaled 0.97 ± 0.06 Tg N year−1during the 2010s, with 94% and 6% from direct and indirect emissions, respectively. Hot spots of soil N2O emission are found in the US Corn Belt and Rice Belt. We find a threefold increase in total soil N2O emission in the United States since 1900, 74% of which is from agricultural soil emissions, increasing by 12 times from 0.04 Tg N year−1in the 1900s to 0.51 Tg N year−1in the 2010s. More than 90% of soil N2O emission increase in agricultural soils is attributed to human land‐use change and agricultural management practices, while increases in N deposition and climate warming are the dominant drivers for N2O emission increase from natural soils. Across the cropped acres, corn production stands out with a large amount of fertilizer consumption and high‐emission factors, responsible for nearly two‐thirds of direct agricultural soil N2O emission increase since 1900. Our study suggests a large N2O mitigation potential in cropland and the importance of exploring crop‐specific mitigation strategies and prioritizing management alternatives for targeted crop types. 
    more » « less
  4. Abstract Soil drying and wetting cycles can produce pulses of nitric oxide (NO) and nitrous oxide (N2O) emissions with substantial effects on both regional air quality and Earth’s climate. While pulsed production of N emissions is ubiquitous across ecosystems, the processes governing pulse magnitude and timing remain unclear. We studied the processes producing pulsed NO and N2O emissions at two contrasting drylands, desert and chaparral, where despite the hot and dry conditions known to limit biological processes, some of the highest NO and N2O flux rates have been measured. We measured N2O and NO emissions every 30 min for 24 h after wetting soils with isotopically-enriched nitrate and ammonium solutions to determine production pathways and their timing. Nitrate was reduced to N2O within 15 min of wetting, with emissions exceeding 1000 ng N–N2O m−2 s−1and returning to background levels within four hours, but the pulse magnitude did not increase in proportion to the amount of ammonium or nitrate added. In contrast to N2O, NO was emitted over 24 h and increased in proportion to ammonium addition, exceeding 600 ng N–NO m−2 s−1in desert and chaparral soils. Isotope tracers suggest that both ammonia oxidation and nitrate reduction produced NO. Taken together, our measurements demonstrate that nitrate can be reduced within minutes of wetting summer-dry desert soils to produce large N2O emission pulses and that multiple processes contribute to long-lasting NO emissions. These mechanisms represent substantial pathways of ecosystem N loss that also contribute to regional air quality and global climate dynamics. 
    more » « less
  5. Abstract Wildfire is an essential earth‐system process, impacting ecosystem processes and the carbon cycle. Forest fires are becoming more frequent and severe, yet gaps exist in the modeling of fire on vegetation and carbon dynamics. Strategies for reducing carbon dioxide (CO2) emissions from wildfires include increasing tree harvest, largely based on the public assumption that fires burn live forests to the ground, despite observations indicating that less than 5% of mature tree biomass is actually consumed. This misconception is also reflected though excessive combustion of live trees in models. Here, we show that regional emissions estimates using widely implemented combustion coefficients are 59%–83% higher than emissions based on field observations. Using unique field datasets from before and after wildfires and an improved ecosystem model, we provide strong evidence that these large overestimates can be reduced by using realistic biomass combustion factors and by accurately quantifying biomass in standing dead trees that decompose over decades to centuries after fire (“snags”). Most model development focuses on area burned; our results reveal that accurately representing combustion is also essential for quantifying fire impacts on ecosystems. Using our improvements, we find that western US forest fires have emitted 851 ± 228 Tg CO2(~half of alternative estimates) over the last 17 years, which is minor compared to 16,200 Tg CO2from fossil fuels across the region. 
    more » « less