| 1. |
- Upstill-Goddard, Robert C., et al.
(författare)
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The riverine source of CH4 and N2O from the Republic of Congo, western Congo Basin
- 2017
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Ingår i: Biogeosciences. - : Copernicus GmbH. - 1726-4170 .- 1726-4189. ; 14:9, s. 2267-2281
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Tidskriftsartikel (refereegranskat)abstract
- We discuss concentrations of dissolved CH4, N2O, O-2, NO(3)(-)and NH4-, and emission fluxes of CH4 and N2O for river sites in the western Congo Basin, Republic of Congo (ROC). Savannah, swamp forest and tropical forest samples were collected from the Congo main stem and seven of its tributaries during November 2010 (41 samples; wet season) and August 2011 (25 samples; dry season; CH4 and N2O only). Dissolved inorganic nitrogen (DIN: NH4- + NO3-; wet season) was dominated by NO3- (63 +/- 19% of DIN). Total DIN concentrations (1.545.3 mu mol L-1) were consistent with the near absence of agricultural, domestic and industrial sources for all three land types. Dissolved O-2 (wet season) was mostly undersaturated in swamp forest (36 +/- 29 %) and tropical forest (77 +/- 36 %) rivers but predominantly supersaturated in savannah rivers (100 +/- 17 %). The dissolved concentrations of CH4 and N2O were within the range of values reported earlier for sub-Saharan African rivers. Dissolved CH4 was found to be supersaturated (11.2-9553 nmol L-1; 440-354 444 %), whereas N2O ranged from strong undersaturation to supersaturation (3.2-20.6 nmol L-1; 47-205 %). Evidently, rivers of the ROC are persistent local sources of CH4 and can be minor sources or sinks for N2O. During the dry season the mean and range of CH4 and N2O concentrations were quite similar for the three land types. Wet and dry season mean concentrations and ranges were not significant for N2O for any land type or for CH4 in savannah rivers. The latter observation is consistent with seasonal buffering of river discharge by an underlying sandstone aquifer. Significantly higher wet season CH4 concentrations in swamp and forest rivers suggest that CH4 can be derived from floating macrophytes during flooding and/or enhanced methanogenesis in adjacent flooded soils. Swamp rivers also exhibited both low (47 %) and high (205 %) N2O saturation but wet season values were overall significantly lower than in either tropical forest or savannah rivers, which were always supersaturated (103-266 %) and for which the overall means and ranges of N2O were not significantly different. In swamp and forest rivers O-2 saturation co-varied inversely with CH4 saturation (log %) and positively with % N2O. A significant positive correlation between N2O and O-2 saturation in swamp rivers was coincident with strong N2O and O-2 undersaturation, indicating N2O consumption during denitrification in the sediments. In savannah rivers persistent N2O supersaturation and a negative correlation between N2O and O-2 suggest N2O production mainly by nitrification. This is consistent with a stronger correlation between N2O and NH4+ than between N2O and NO3-. Our ranges of values for CH4 and N2O emission fluxes (33-48 705 mu mol CH4 m(-2) d(-1); 1-67 mu mol N(2)Om(2)(-) d(-1)) are within the ranges previously estimated for sub-Saharan African rivers but they include uncertainties deriving from our use of basin-wide values for CH4 and N2O gas transfer velocities. Even so, because we did not account for any contribution from ebullition, which is quite likely for CH4 (at least 20 %), we consider our emission fluxes for CH4 to be conservative.
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| 2. |
- Wilson, Samuel T., et al.
(författare)
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Ideas and perspectives : A strategic assessment of methane and nitrous oxide measurements in the marine environment
- 2020
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Ingår i: Biogeosciences. - : Copernicus GmbH. - 1726-4170 .- 1726-4189. ; 17:22, s. 5809-5828
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Tidskriftsartikel (refereegranskat)abstract
- In the current era of rapid climate change, accurate characterization of climate-relevant gas dynamics – namely production, consumption, and net emissions – is required for all biomes, especially those ecosystems most susceptible to the impact of change. Marine environments include regions that act as net sources or sinks for numerous climate-active trace gases including methane (CH4) and nitrous oxide (N2O). The temporal and spatial distributions of CH4 and N2O are controlled by the interaction of complex biogeochemical and physical processes. To evaluate and quantify how these mechanisms affect marine CH4 and N2O cycling requires a combination of traditional scientific disciplines including oceanography, microbiology, and numerical modeling. Fundamental to these efforts is ensuring that the datasets produced by independent scientists are comparable and interoperable. Equally critical is transparent communication within the research community about the technical improvements required to increase our collective understanding of marine CH4 and N2O. A workshop sponsored by Ocean Carbon and Biogeochemistry (OCB) was organized to enhance dialogue and collaborations pertaining to marine CH4 and N2O. Here, we summarize the outcomes from the workshop to describe the challenges and opportunities for near-future CH4 and N2O research in the marine environment.
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| 3. |
- Kitidis, V., et al.
(författare)
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Methane and nitrous oxide in surface water along the North-West Passage, Arctic Ocean
- 2010
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Ingår i: Marine Chemistry. - : Elsevier BV. - 0304-4203. ; 121:1-4, s. 80-86
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Tidskriftsartikel (refereegranskat)abstract
- Dissolved methane and nitrous oxide in seawater were measured along a 6700 km transect of the North-West Passage between the North Atlantic Ocean and Beaufort Sea in the Arctic Ocean. Over- and under-saturation with respect to atmospheric equilibrium were observed for both gases. Methane and nitrous oxide were in the range of 58–528% and 82–181% saturation, respectively. Under-saturation was attributed to melt-water with low methane and nitrous oxide, while over-saturation was found under multi-year sea-ice. Elevated methane was also found in the vicinity of the marginal ice zones and the Mackenzie River plume. Our data support both water column and sedimentary sources of methane and nitrous oxide. We found first-order methane oxidation in surface seawater with a rate constant of 3.8 × 10−3 h−1. Based on these results and a conceptual model, we suggest that future sea-ice retreat may decrease the residence times of methane and nitrous oxide in the surface Arctic Ocean and thus enhance the sea–air flux of these climatically active gases.
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| 4. |
- Stolle, Christian, et al.
(författare)
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The MILAN Campaign : Studying Diel Light Effects on the Air–Sea Interface
- 2020
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Ingår i: Bulletin of The American Meteorological Society - (BAMS). - 0003-0007 .- 1520-0477. ; 101:2, s. E146-E166
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Tidskriftsartikel (refereegranskat)abstract
- The sea surface microlayer (SML) at the air–sea interface is <1 mm thick, but it is physically, chemically, and biologically distinct from the underlying water and the atmosphere above. Wind-driven turbulence and solar radiation are important drivers of SML physical and biogeochemical properties. Given that the SML is involved in all air–sea exchanges of mass and energy, its response to solar radiation, especially in relation to how it regulates the air–sea exchange of climate-relevant gases and aerosols, is surprisingly poorly characterized. MILAN (Sea Surface Microlayer at Night) was an international, multidisciplinary campaign designed to specifically address this issue. In spring 2017, we deployed diverse sampling platforms (research vessels, radio-controlled catamaran, free-drifting buoy) to study full diel cycles in the coastal North Sea SML and in underlying water, and installed a land-based aerosol sampler. We also carried out concurrent ex situ experiments using several microsensors, a laboratory gas exchange tank, a solar simulator, and a sea spray simulation chamber. In this paper we outline the diversity of approaches employed and some initial results obtained during MILAN. Our observations of diel SML variability show, for example, an influence of (i) changing solar radiation on the quantity and quality of organic material and (ii) diel changes in wind intensity primarily forcing air–sea CO2 exchange. Thus, MILAN underlines the value and the need of multidiciplinary campaigns for integrating SML complexity into the context of air–sea interaction.
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