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1. North American boreal forests are a large carbon source due to wildfires from 1986 to 2016

   https://doi.org/10.1038/s41598-021-87343-3  

   Zhao, Bailu ; Zhuang, Qianlai ; Shurpali, Narasinha ; Köster, Kajar ; Berninger, Frank ; Pumpanen, Jukka ( December 2021 , Scientific Reports)

   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. 

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2. Seasonality and Budgets of Soil Greenhouse Gas Emissions From a Tropical Dry Forest Successional Gradient in Costa Rica

   https://doi.org/10.1029/2020JG005647  

   Calvo‐Rodriguez, Sofia ; Kiese, Ralf ; Sánchez‐Azofeifa, G. Arturo ( September 2020 , Journal of Geophysical Research: Biogeosciences)

   Limited information on greenhouse gas emissions from tropical dry forest soils still hinders the assessment of the sources/sinks from this ecosystem and their contribution at global scales. Particularly, rewetting events after the dry season can have a significant effect on soil biogeochemical processes and associated exchange of greenhouse gases. This study evaluated the temporal variation and annual fluxes of CO₂, N₂O, and CH₄from soils in a tropical dry forest successional gradient. After a prolonged drought of 5 months, large emissions pulses of CO₂and N₂O were observed at all sites following first rain events, caused by the “Birch effect,” with a significant effect on the net ecosystem exchange and the annual emissions budget. Annual CO₂emissions were greatest for the young forest (8,556 kg C ha⁻¹yr⁻¹) followed by the older forest (7,420 kg C ha⁻¹yr⁻¹) and the abandoned pasture (7,224 kg C ha⁻¹yr⁻¹). Annual emissions of N₂O were greatest for the forest sites (0.39 and 0.43 kg N ha⁻¹yr⁻¹) and least in the abandoned pasture (0.09 kg N ha⁻¹yr⁻¹). CH₄uptake was greatest in the older forest (−2.61 kg C ha⁻¹yr⁻¹) followed by the abandoned pasture (−0.69 kg C ha⁻¹yr⁻¹) and the young forest (−0.58 kg C ha⁻¹yr⁻¹). Fluxes were mainly influenced by soil moisture, microbial biomass, and soil nitrate and ammonium concentrations. Annual CO₂and N₂O soil fluxes of tropical dry forests in this study and others from the literature were much lower than the annual fluxes in wetter tropical forests. Conversely, tropical dry forests and abandoned pastures are on average stronger sinks for CH₄than wetter tropical forests.

    

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3. Fixing a snag in carbon emissions estimates from wildfires

   https://doi.org/10.1111/gcb.14716  

   Stenzel, Jeffrey E. ; Bartowitz, Kristina J. ; Hartman, Melannie D. ; Lutz, James A. ; Kolden, Crystal A. ; Smith, Alistair M. S. ; Law, Beverly E. ; Swanson, Mark E. ; Larson, Andrew J. ; Parton, William J. ; et al ( July 2019 , Global Change Biology)

   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.

    

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4. Little Effect of Land Use on N 2 O and NO Emission Pulses Following Rewetting of Dry Soils Across Seasonally Dry sub‐Saharan Africa

   https://doi.org/10.1029/2020JG005742  

   Hickman, Jonathan E. ; Kaya, Bocary ; Kebede, Abhraham ; Kandji, Serigne ; Fitch, Laura ; Neill, Christopher ; Nyadzi, Gerson ; Diru, Willy ; Palm, Cheryl A. ( January 2021 , Journal of Geophysical Research: Biogeosciences)

   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.

    

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5. Rapid nitrate reduction produces pulsed NO and N2O emissions following wetting of dryland soils

   https://doi.org/10.1007/s10533-022-00896-x  

   Krichels, Alexander H. ; Homyak, Peter M. ; Aronson, Emma L. ; Sickman, James O. ; Botthoff, Jon ; Shulman, Hannah ; Piper, Stephanie ; Andrews, Holly M. ; Jenerette, G. Darrel ( February 2022 , Biogeochemistry)

   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.

    

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