Biogeochemical and physical controls on the evolution of dissolved inorganic carbon (DIC) and δ13CDIC in karst spring-waters exposed to atmospheric CO2(g): Insights from laboratory experiments

2020 ◽  
Vol 583 ◽  
pp. 124294 ◽  
Author(s):  
Yongjun Jiang ◽  
Jiaqi Lei ◽  
Liuchan Hu ◽  
Qiong Xiao ◽  
Jinliang Wang ◽  
...  
Keyword(s):  
Laboratory Experiments ◽  
Inorganic Carbon ◽  
Dissolved Inorganic Carbon ◽  
Atmospheric Co2 ◽  
Karst Spring ◽  
Physical Controls

scholarly journals Increase of 14C Activity of Dissolved Inorganic Carbon Along a River Course

Radiocarbon ◽  
1986 ◽  
Vol 28 (2A) ◽  
pp. 515-521 ◽  
Author(s):  
Dušan Srdoč ◽  
Ines Krajcar-Bronić ◽  
Nada Horvatinčić ◽  
Bogomil Obelić
Keyword(s):  
Aquatic Plants ◽  
Water Samples ◽  
Organic Material ◽  
Root Respiration ◽  
Inorganic Carbon ◽  
Dissolved Inorganic Carbon ◽  
Stream Water ◽  
Exchange Process ◽  
Karst Spring ◽  
Stream Waters

Results of measurements for 3 years (1981–1983) of 14C activity of dissolved inorganic carbon (DIG) in water samples from the Korana River, as well as that of recent tufa and aquatic plants, showed that 14C concentration increases from karst spring to the estuary. A model describing the increase of 14C activity was developed assuming that the increase is due to the exchange of the dissolved CO2 in stream water with atmospheric CO2 and to dissolution of CO2 from the decay of organic material and root respiration. It is possible to distinguish these two contributions by measuring the δ13C values of DIC in water. As expected, our data show that the exchange process between atmospheric CO2 and DIC dominates at rapids and waterfalls, while biologic contribution is much higher in lakes and along the lowland flow of the Korana River. Agreement between the calculated and the measured activities supports the proposed mechanisms of chemical and isotopic exchanges in stream waters.

scholarly journals Radiocarbon isotopic evidence for assimilation of atmospheric CO<sub>2</sub> by the seagrass <i>Zostera marina</i>

2015 ◽  
Vol 12 (20) ◽  
pp. 6251-6258 ◽  
Author(s):  
K. Watanabe ◽  
T. Kuwae
Keyword(s):  
Carbon Source ◽  
Zostera Marina ◽  
Inorganic Carbon ◽  
Aquatic Vegetation ◽  
Dissolved Inorganic Carbon ◽  
Isotope Analysis ◽  
Co2 Exchange ◽  
Atmospheric Co2 ◽  
Isotopic Signatures ◽  
Seagrass Meadows

Abstract. Submerged aquatic vegetation takes up water-column dissolved inorganic carbon (DIC) as a carbon source across its thin cuticle layer. It is expected that marine macrophytes also use atmospheric CO2 when exposed to air during low tide, although assimilation of atmospheric CO2 has never been quantitatively evaluated. Using the radiocarbon isotopic signatures (Δ14C) of the seagrass Zostera marina, DIC and particulate organic carbon (POC), we show quantitatively that Z. marina takes up and assimilates atmospheric modern CO2 in a shallow coastal ecosystem. The Δ14C values of the seagrass (−40 to −10 ‰) were significantly higher than those of aquatic DIC (−46 to −18 ‰), indicating that the seagrass uses a 14C-rich carbon source (atmospheric CO2, +17 ‰). A carbon-source mixing model indicated that the seagrass assimilated 0–40 % (mean, 17 %) of its inorganic carbon as atmospheric CO2. CO2 exchange between the air and the seagrass might be enhanced by the presence of a very thin film of water over the air-exposed leaves during low tide. Our radiocarbon isotope analysis, showing assimilation of atmospheric modern CO2 as an inorganic carbon source, improves our understanding of the role of seagrass meadows in coastal carbon dynamics.

scholarly journals Inorganic carbon fluxes across the vadose zone of planted and unplanted soil mesocosms

2014 ◽  
Vol 11 (3) ◽  
pp. 4251-4299 ◽  
Author(s):  
E. M. Thaysen ◽  
D. Jacques ◽  
S. Jessen ◽  
C. E. Andersen ◽  
E. Laloy ◽  
...  
Keyword(s):  
Carbon Dioxide ◽  
Vadose Zone ◽  
Inorganic Carbon ◽  
Plant Biomass ◽  
Dissolved Inorganic Carbon ◽  
Carbon Fluxes ◽  
Atmospheric Co2 ◽  
Carbon Dioxide Partial Pressure ◽  
Post Harvest ◽  
Unplanted Soil

Abstract. The efflux of carbon dioxide (CO2) from soils influences atmospheric CO2 concentrations and thereby climate change. The partitioning of inorganic carbon fluxes in the vadose zone between emission to the atmosphere and to the groundwater was investigated. Carbon dioxide partial pressure in the soil gas (pCO2), alkalinity, soil moisture and temperature were measured over depth and time in unplanted and planted (barley) mesocosms. The dissolved inorganic carbon (DIC) percolation flux was calculated from the pCO2, alkalinity and the water flux at the mesocosm bottom. Carbon dioxide exchange between the soil surface and the atmosphere was measured at regular intervals. The soil diffusivity was determined from soil radon-222 (222Rn) emanation rates and soil air Rn concentration profiles, and was used in conjunction with measured pCO2 gradients to calculate the soil CO2 production. Carbon dioxide fluxes were modelled using the HP1 module of the Hydrus 1-D software. The average CO2 effluxes to the atmosphere from unplanted and planted mesocosm ecosystems during 78 days of experiment were 0.1 ± 0.07 and 4.9 ± 0.07 μmol carbon (C) m−2 s−1, respectively, and largely exceeded the corresponding DIC percolation fluxes of 0.01 ± 0.004 and 0.06 ± 0.03 μmol C m−2 s−1. Post-harvest soil respiration (Rs) was only 10% of the Rs during plant growth, while the post-harvest DIC percolation flux was more than one third of the flux during growth. The Rs was controlled by production and diffusivity of CO2 in the soil. The DIC percolation flux was largely controlled by the pCO2 and the drainage flux due to low solution pH. Plant biomass and soil pCO2 were high in the mesocosms as compared to a standard field situation. Our results indicate no change of the cropland C balance under elevated atmospheric CO2 in a warmer future climate, in which plant biomass and soil pCO2 are expected to increase.

scholarly journals Reviews and Syntheses: Ocean acidification and its potential impacts on marine ecosystems

2015 ◽  
Vol 12 (13) ◽  
pp. 10939-10983 ◽  
Author(s):  
K. M. G. Mostofa ◽  
C.-Q. Liu ◽  
W. D. Zhai ◽  
M. Minella ◽  
D. Vione ◽  
...  
Keyword(s):  
Ocean Acidification ◽  
Algal Blooms ◽  
Inorganic Carbon ◽  
Dissolved Inorganic Carbon ◽  
Marine Organisms ◽  
Atmospheric Co2 ◽  
Algal Toxins ◽  
Seawater Ph ◽  
Potential Impact ◽  
Insight Into

Abstract. Ocean acidification, a complex phenomenon that lowers seawater pH, is the net outcome of several contributions. They include the dissolution of increasing atmospheric CO2 that adds up with dissolved inorganic carbon (dissolved CO2, H2CO3, HCO3−, and CO32−) generated upon mineralization of primary producers (PP) and dissolved organic matter (DOM). The aquatic processes leading to inorganic carbon are substantially affected by increased DOM and nutrients via terrestrial runoff, acidic rainfall, increased PP and algal blooms, nitrification, denitrification, sulfate reduction, global warming (GW), and by atmospheric CO2 itself through enhanced photosynthesis. They are consecutively associated with enhanced ocean acidification, hypoxia in acidified deeper seawater, pathogens, algal toxins, oxidative stress by reactive oxygen species, and thermal stress caused by longer stratification periods as an effect of GW. We discuss the mechanistic insights into the aforementioned processes and pH changes, with particular focus on processes taking place with different time scales (including the diurnal one) in surface and subsurface seawater. This review also discusses these collective influences to assess their potential detrimental effects to marine organisms, and of ecosystem processes and services. Our review of the effects operating in synergy with ocean acidification will provide a broad insight into the potential impact of acidification itself on biological processes. The foreseen danger to marine organisms by acidification is in fact expected to be amplified by several concurrent and interacting phenomena.

Seasonal dissolved inorganic carbon variations in the Greenland Sea and implications for atmospheric CO2 exchange

1999 ◽  
Vol 46 (6-7) ◽  
pp. 1473-1496 ◽  
Author(s):  
Lisa A. Miller ◽  
Melissa Chierici ◽  
Truls Johannessen ◽  
Thomas T. Noji ◽  
Francisco Rey ◽  
...  
Keyword(s):  
Inorganic Carbon ◽  
Dissolved Inorganic Carbon ◽  
Co2 Exchange ◽  
Atmospheric Co2 ◽  
Greenland Sea

scholarly journals Reviews and Syntheses: Ocean acidification and its potential impacts on marine ecosystems

2016 ◽  
Vol 13 (6) ◽  
pp. 1767-1786 ◽  
Author(s):  
Khan M. G. Mostofa ◽  
Cong-Qiang Liu ◽  
WeiDong Zhai ◽  
Marco Minella ◽  
Davide Vione ◽  
...  
Keyword(s):  
Ocean Acidification ◽  
Algal Blooms ◽  
Inorganic Carbon ◽  
Dissolved Inorganic Carbon ◽  
Marine Organisms ◽  
Atmospheric Co2 ◽  
Algal Toxins ◽  
Seawater Ph ◽  
Potential Impact ◽  
Insight Into

Abstract. Ocean acidification, a complex phenomenon that lowers seawater pH, is the net outcome of several contributions. They include the dissolution of increasing atmospheric CO2 that adds up with dissolved inorganic carbon (dissolved CO2, H2CO3, HCO3−, and CO32−) generated upon mineralization of primary producers (PP) and dissolved organic matter (DOM). The aquatic processes leading to inorganic carbon are substantially affected by increased DOM and nutrients via terrestrial runoff, acidic rainfall, increased PP and algal blooms, nitrification, denitrification, sulfate reduction, global warming (GW), and by atmospheric CO2 itself through enhanced photosynthesis. They are consecutively associated with enhanced ocean acidification, hypoxia in acidified deeper seawater, pathogens, algal toxins, oxidative stress by reactive oxygen species, and thermal stress caused by longer stratification periods as an effect of GW. We discuss the mechanistic insights into the aforementioned processes and pH changes, with particular focus on processes taking place with different timescales (including the diurnal one) in surface and subsurface seawater. This review also discusses these collective influences to assess their potential detrimental effects to marine organisms, and of ecosystem processes and services. Our review of the effects operating in synergy with ocean acidification will provide a broad insight into the potential impact of acidification itself on biological processes. The foreseen danger to marine organisms by acidification is in fact expected to be amplified by several concurrent and interacting phenomena.

scholarly journals Abiotic methane formation during experimental serpentinization of olivine

2016 ◽  
Vol 113 (49) ◽  
pp. 13965-13970 ◽  
Author(s):  
Thomas M. McCollom
Keyword(s):  
Laboratory Experiments ◽  
Inorganic Carbon ◽  
Dissolved Inorganic Carbon ◽  
Methane Formation ◽  
Natural Systems ◽  
Abiotic Synthesis ◽  
Inorganic Carbon Source ◽  
Abiotic Reduction ◽  
Abiotic Methane ◽  
Kinetic Barriers

Fluids circulating through actively serpentinizing systems are often highly enriched in methane (CH4). In many cases, the CH4 in these fluids is thought to derive from abiotic reduction of inorganic carbon, but the conditions under which this process can occur in natural systems remain unclear. In recent years, several studies have reported abiotic formation of CH4 during experimental serpentinization of olivine at temperatures at or below 200 °C. However, these results seem to contradict studies conducted at higher temperatures (300 °C to 400 °C), where substantial kinetic barriers to CH4 synthesis have been observed. Here, the potential for abiotic formation of CH4 from dissolved inorganic carbon during olivine serpentinization is reevaluated in a series of laboratory experiments conducted at 200 °C to 320 °C. A 13C-labeled inorganic carbon source was used to unambiguously determine the origin of CH4 generated in the experiments. Consistent with previous high-temperature studies, the results indicate that abiotic formation of CH4 from reduction of dissolved inorganic carbon during the experiments is extremely limited, with nearly all of the observed CH4 derived from background sources. The results indicate that the potential for abiotic synthesis of CH4 in low-temperature serpentinizing environments may be much more limited than some recent studies have suggested. However, more extensive production of CH4 was observed in one experiment performed under conditions that allowed an H2-rich vapor phase to form, suggesting that shallow serpentinization environments where a separate gas phase is present may be more favorable for abiotic synthesis of CH4.

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