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1. Contemporary decline in northern Indian Ocean primary production offset by rising atmospheric nitrogen deposition

   https://doi.org/10.3389/fmars.2024.1418634  

   Malsang, Manon; Resplandy, Laure; Bopp, Laurent; Zhao, Yangyang; Ditkovsky, Sam; Yang, Fan; Paulot, Fabien; Lévy, Marina (December 2024, Frontiers in Marine Science)

   Since 1980, atmospheric pollutants in South Asia and India have dramatically increased in response to industrialization and agricultural development, enhancing the atmospheric deposition of anthropogenic nitrogen in the northern Indian Ocean and potentially promoting primary productivity. Concurrently, ocean warming has increased stratification and limited the supply of nutrients supporting primary productivity. Here, we examine the biogeochemical consequences of increasing anthropogenic atmospheric nitrogen deposition and contrast them with the counteracting effect of warming, using a regional ocean biogeochemical model of the northern Indian Ocean forced with atmospheric nitrogen deposition derived from an Earth System Model. Our results suggest that the 60% recent increase in anthropogenic nitrogen deposition over the northern Indian Ocean provided external reactive nitrogen that only weakly enhanced primary production (+10 mg C.m^–2.d^–1.yr^–1in regions of intense deposition) and secondary production (+4 mg C.m^–2.d^–1.yr^–1). However, we find that locally this enhancement can significantly offset the declining trend in primary production over the last four decades in the central Arabian Sea and western Bay of Bengal, whose magnitude are up to -20 and -10 mg C.m^–2.d^–1.yr^–1respectively. 

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2. Acclimation of Phytoplankton Fe:C Ratios Dampens the Biogeochemical Response to Varying Atmospheric Deposition of Soluble Iron

   https://doi.org/10.1029/2022GB007491  

   Wiseman, N A; Moore, J K; Twining, B S; Hamilton, D S; Mahowald, N M (April 2023, Global Biogeochemical Cycles)

   Abstract Dissolved iron (dFe) plays an important role in regulating marine productivity. In high nutrient, low chlorophyll regions (>33% of the global ocean), iron is the primary growth limiting nutrient, and elsewhere iron can regulate nitrogen fixation by diazotrophs. The link between iron availability and carbon export is strongly dependent on the phytoplankton iron quotas or cellular Fe:C ratios. This ratio varies by more than an order of magnitude in the open ocean and is positively correlated with ambient dFe concentrations in field observations. Representing Fe:C ratios within models is necessary to investigate how ocean carbon cycling will interact with perturbations to iron cycling in a changing climate. The Community Earth System Model ocean component was modified to simulate dynamic, group‐specific, phytoplankton Fe:C that varies as a function of ambient iron concentration. The simulated Fe:C ratios improve the representation of the spatial trends in the observed Fe:C ratios. The acclimation of phytoplankton Fe:C ratios dampens the biogeochemical response to varying atmospheric deposition of soluble iron, compared to a fixed Fe:C ratio. However, varying atmospheric soluble iron supply has first order impacts on global carbon and nitrogen fluxes and on nutrient limitation spatial patterns. Our results suggest that pyrogenic Fe is a significant dFe source that rivals mineral dust inputs in some regions. Changes in dust flux and iron combustion sources (anthropogenic and wildfires) will modify atmospheric Fe inputs in the future. Accounting for dynamic phytoplankton iron quotas is critical for understanding ocean biogeochemistry and projecting its response to variations in atmospheric deposition. 

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3. Net greenhouse gas balance in U.S. croplands: How can soils be part of the climate solution?

   https://doi.org/10.1111/gcb.17109  

   You, Yongfa; Tian, Hanqin; Pan, Shufen; Shi, Hao; Lu, Chaoqun; Batchelor, William D; Cheng, Bo; Hui, Dafeng; Kicklighter, David; Liang, Xin‐Zhong; et al (January 2024, Global Change Biology)

   Abstract Agricultural soils play a dual role in regulating the Earth's climate by releasing or sequestering carbon dioxide (CO₂) in soil organic carbon (SOC) and emitting non‐CO₂greenhouse gases (GHGs) such as nitrous oxide (N₂O) and methane (CH₄). To understand how agricultural soils can play a role in climate solutions requires a comprehensive assessment of net soil GHG balance (i.e., sum of SOC‐sequestered CO₂and non‐CO₂GHG emissions) and the underlying controls. Herein, we used a model‐data integration approach to understand and quantify how natural and anthropogenic factors have affected the magnitude and spatiotemporal variations of the net soil GHG balance in U.S. croplands during 1960–2018. Specifically, we used the dynamic land ecosystem model for regional simulations and used field observations of SOC sequestration rates and N₂O and CH₄emissions to calibrate, validate, and corroborate model simulations. Results show that U.S. agricultural soils sequestered Tg CO₂‐C year⁻¹in SOC (at a depth of 3.5 m) during 1960–2018 and emitted Tg N₂O‐N year⁻¹and Tg CH₄‐C year⁻¹, respectively. Based on the GWP100 metric (global warming potential on a 100‐year time horizon), the estimated national net GHG emission rate from agricultural soils was Tg CO₂‐eq year⁻¹, with the largest contribution from N₂O emissions. The sequestered SOC offset ~28% of the climate‐warming effects resulting from non‐CO₂GHG emissions, and this offsetting effect increased over time. Increased nitrogen fertilizer use was the dominant factor contributing to the increase in net GHG emissions during 1960–2018, explaining ~47% of total changes. In contrast, reduced cropland area, the adoption of agricultural conservation practices (e.g., reduced tillage), and rising atmospheric CO₂levels attenuated net GHG emissions from U.S. croplands. Improving management practices to mitigate N₂O emissions represents the biggest opportunity for achieving net‐zero emissions in U.S. croplands. Our study highlights the importance of concurrently quantifying SOC‐sequestered CO₂and non‐CO₂GHG emissions for developing effective agricultural climate change mitigation measures. 

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4. Bacterial denitrification drives elevated N ₂ O emissions in arid southern California drylands

   https://doi.org/10.1126/sciadv.adj1989  

   Krichels, Alexander H; Jenerette, G Darrel; Shulman, Hannah; Piper, Stephanie; Greene, Aral C; Andrews, Holly M; Botthoff, Jon; Sickman, James O; Aronson, Emma L; Homyak, Peter M (December 2023, Science Advances)

   Soils are the largest source of atmospheric nitrous oxide (N₂O), a powerful greenhouse gas. Dry soils rarely harbor anoxic conditions to favor denitrification, the predominant N₂O-producing process, yet, among the largest N₂O emissions have been measured after wetting summer-dry desert soils, raising the question: Can denitrifiers endure extreme drought and produce N₂O immediately after rainfall? Using isotopic and molecular approaches in a California desert, we found that denitrifiers produced N₂O within 15 minutes of wetting dry soils (site preference = 12.8 ± 3.92 per mil, δ¹⁵N^bulk= 18.6 ± 11.1 per mil). Consistent with this finding, we detected nitrate-reducing transcripts in dry soils and found that inhibiting microbial activity decreased N₂O emissions by 59%. Our results suggest that despite extreme environmental conditions—months without precipitation, soil temperatures of ≥40°C, and gravimetric soil water content of <1%—bacterial denitrifiers can account for most of the N₂O emitted when dry soils are wetted. 

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5. Quantifying Gross Rates of Methane Production and Consumption in a Northern Forest

   Kahn, Dana; Savage, Kathleen E; Cadillo-Quiroz, Hinsby; Fraver, Shawn; Watts, Jennifer; Xu, Xiaofeng; Sihi, Debjani (December 2024, American Geophysical Union)

   Northern forest soils are vital for climate change mitigation since upland sandy soils favor the net consumption/oxidation of atmospheric methane (CH4). We are studying biogeochemical CH4 cycle processes in a Northern Forest (Howland Research Forest, Maine), where upland soils are interspersed with wetland (Sphagnum bog), and upland-wetland transition soils along with hummock-hollow microtopography. This complex mosaic of microsites with sources and sinks of CH4 is subjected to change under future wet climates projected for this region, with a potential for these forests to shift from a net CH4 sink to a net CH4 source. Net CH4 emissions in a wet climate can increase either by inhibiting methanotrophs or favoring methanogens, or both. Thus, quantifying underlying processes of gross CH4 production and consumption can reduce the uncertainty of CH4 sink/source estimation in this critical ecosystem. We have collected baseline soil data across the forest's landscape including Total Carbon and Total Nitrogen with the Elemental Analyzer, Gravimetric Soil Moisture, and pH. Furthermore, stable isotope dilution method will serve as a proxy for methanogenic and methanotrophic activities to quantify gross rates of CH4 production and consumption from a flooding (wet-up) experiment in Howland Forest. We will differentiate between CH4 consumption and production by measuring both the change in the amount of CH4 and the ratio between labeled and unlabeled CH4 in a closed system. We will analyze the stable C isotope in 13CH4 to determine gross rates of CH4 production and oxidation in situ and within laboratory incubations. The in situ stable isotope dilution technique will be compared with the gas push-pull method, to test the suitability of a simple, low cost method to quantify gross CH4 oxidation rates. Novel data obtained in this study will constrain CH4 cycle processes in a biogeochemical model to quantify CH4 source-sink potential in Northern Forests under current and future climatic conditions. 

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