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: Advances in understanding of air–sea exchange and cycling of greenhouse gases in the upper ocean
The air–sea exchange and oceanic cycling of greenhouse gases (GHG), including carbon dioxide (CO2), nitrous oxide (N2O), methane (CH4), carbon monoxide (CO), and nitrogen oxides (NOx = NO + NO2), are fundamental in controlling the evolution of the Earth’s atmospheric chemistry and climate. Significant advances have been made over the last 10 years in understanding, instrumentation and methods, as well as deciphering the production and consumption pathways of GHG in the upper ocean (including the surface and subsurface ocean down to approximately 1000 m). The global ocean under current conditions is now well established as a major sink for CO2, a major source for N2O and a minor source for both CH4 and CO. The importance of the ocean as a sink or source of NOx is largely unknown so far. There are still considerable uncertainties about the processes and their major drivers controlling the distributions of N2O, CH4, CO, and NOx in the upper ocean. Without having a fundamental understanding of oceanic GHG production and consumption pathways, our knowledge about the effects of ongoing major oceanic changes—warming, acidification, deoxygenation, and eutrophication—on the oceanic cycling and air–sea exchange of GHG remains rudimentary at best. We suggest that only through a comprehensive, coordinated, and interdisciplinary approach that includes data collection by global observation networks as well as joint process studies can the necessary data be generated to (1) identify the relevant microbial and phytoplankton communities, (2) quantify the rates of ocean GHG production and consumption pathways, (3) comprehend their major drivers, and (4) decipher economic and cultural implications of mitigation solutions.  more » « less
Award ID(s):
1840868
PAR ID:
10534759
Author(s) / Creator(s):
; ; ; ; ; ; ; ; ; ; ; ; ; ; ;
Publisher / Repository:
University of California Press
Date Published:
Journal Name:
Elem Sci Anth
Volume:
12
Issue:
1
ISSN:
2325-1026
Format(s):
Medium: X
Sponsoring Org:
National Science Foundation
More Like this
  1. ; ; ; ; ; ; ; ; ; (, Elem Sci Anth)
    Major coastal upwelling systems are among the most productive marine ecosystems in the world. They contribute disproportionately to the cycling of carbon and nutrients in the ocean and influence marine biogeochemistry beyond their productive regions. Characterized by intense microbial respiration (both aerobic and anaerobic), major coastal upwelling systems are also hotspots for the production and outgassing of potent greenhouse gases (GHG) such as CO2, N2O, and CH4. Quantifying and understanding these roles in the context of a changing climate is therefore a subject of great interest. Here we provide a short synthesis of the current knowledge of the contributions of major coastal upwelling systems to the cycling of GHG. Despite variations within and among different systems, low-latitude coastal upwelling systems typically act as a net carbon source to the atmosphere, while those at higher latitudes function as weak sinks or remain neutral regarding atmospheric CO2. These systems also significantly contribute to oceanic N2O and CH4 emissions, although the extent of their contribution to the latter remains poorly constrained. We also overview recent and future changes to upwelling systems in the context of a warmer climate and discuss uncertainties and implications for GHG production. Although rapid coastal warming is anticipated in all major coastal upwelling systems, the future changes in upwelling-favorable winds and their implications within the context of increased stratification are uncertain. Finally, we examine the major challenges that impede our ability to accurately predict how major coastal upwelling systems will respond to future climate change, and present recommendations for future research to better capture ongoing changes and disentangle natural and forced variability. 
    more » « less
  2. ; ; ; ; ; ; ; ; ; ; et al (, Nature Climate Change)
    Rapid climate warming and sea-ice loss have induced major changes in the sea surface partial pressure of CO2 ( pCO2I). However, the long-term trends in the western Arctic Ocean are unknown. Here we show that in 1994–2017, summer pCO2I in the Canada Basin increased at twice the rate of atmospheric increase. Warming and ice loss in the basin have strengthened the pCO2I seasonal amplitude, resulting in the rapid decadal increase. Consequently, the summer air–sea CO2 gradient has reduced rapidly, and may become near zero within two decades. In contrast, there was no significant pCO2I increase on the Chukchi Shelf, where strong and increasing biological uptake has held pCO2I low, and thus the CO2 sink has increased and may increase further due to the atmospheric CO2 increase. Our findings elucidate the contrasting physical and biological drivers controlling sea surface pCO2I variations and trends in response to climate change in the Arctic Ocean. 
    more » « less
  3. ; ; ; ; ; ; ; (, npj Climate and Atmospheric Science)
    Abstract The strength and variability of the Southern Ocean carbon sink is a significant source of uncertainty in the global carbon budget. One barrier to reconciling observations and models is understanding how synoptic weather patterns modulate air-sea carbon exchange. Here, we identify and track storms using atmospheric sea level pressure fields from reanalysis data to assess the role that storms play in driving air-sea CO2exchange. We examine the main drivers of CO2fluxes under storm forcing and quantify their contribution to Southern Ocean annual air-sea CO2fluxes. Our analysis relies on a forced ocean-ice simulation from the Community Earth System Model, as well as CO2fluxes estimated from Biogeochemical Argo floats. We find that extratropical storms in the Southern Hemisphere induce CO2outgassing, driven by CO2disequilibrium. However, this effect is an order of magnitude larger in observations compared to the model and caused by different reasons. Despite large uncertainties in CO2fluxes and storm statistics, observations suggest a pivotal role of storms in driving Southern Ocean air-sea CO2outgassing that remains to be well represented in climate models, and needs to be further investigated in observations. 
    more » « less
  4. ; ; (, Journal of Marine Science and Engineering)
    The air–sea exchange of carbon dioxide (CO2) on a global scale is a key factor in understanding climate change and predicting its effects. The magnitude of sea spray’s contribution to this flux is currently highly uncertain. Constraining CO2’s diffusion in sea spray droplets is important for reducing error margins in global estimates of oceanic CO2 uptake and release. The timescale for CO2 gas diffusion within sea spray is known to be shorter than the timescales for the droplets’ physical changes to take place while aloft. However, the rate of aqueous carbonate reactions relative to these timescales has not been assessed. This study investigates the timescales of droplet physical changes to those of chemical transformations across the H2CO3/HCO3−/CO32− sequence. We found that physical timescales are rate limiting and that evaporation drives carbonate species into gaseous CO2, promoting the production and evasion of CO2 from sea spray droplets. This has important implications for carbon cycling and feedback in the surface ocean. 
    more » « less
  5. ; ; ; ; ; ; ; ; ; ; et al (, Biogeosciences)
    null (Ed.)
    Abstract. In the current era of rapid climate change, accuratecharacterization of climate-relevant gas dynamics – namely production,consumption, and net emissions – is required for all biomes, especially thoseecosystems most susceptible to the impact of change. Marine environmentsinclude regions that act as net sources or sinks for numerous climate-activetrace gases including methane (CH4) and nitrous oxide (N2O). Thetemporal and spatial distributions of CH4 and N2O are controlledby the interaction of complex biogeochemical and physical processes. Toevaluate and quantify how these mechanisms affect marine CH4 andN2O cycling requires a combination of traditional scientificdisciplines including oceanography, microbiology, and numerical modeling.Fundamental to these efforts is ensuring that the datasets produced byindependent scientists are comparable and interoperable. Equally critical istransparent communication within the research community about the technicalimprovements required to increase our collective understanding of marineCH4 and N2O. A workshop sponsored by Ocean Carbon and Biogeochemistry (OCB)was organized to enhance dialogue and collaborations pertaining tomarine CH4 and N2O. Here, we summarize the outcomes from theworkshop to describe the challenges and opportunities for near-futureCH4 and N2O research in the marine environment. 
    more » « less
  • Citation Formats
  • MLA
  • APA
  • Chicago
  • BibTeX
  • Save / Share this Record
  • Send to Email