scholarly journals Global surface-ocean <i>p</i><sup>CO<sub>2</sub></sup> and sea–air CO<sub>2</sub> flux variability from an observation-driven ocean mixed-layer scheme

Ocean Science ◽  
2013 ◽  
Vol 9 (2) ◽  
pp. 193-216 ◽  
Author(s):  
C. Rödenbeck ◽  
R. F. Keeling ◽  
D. C. E. Bakker ◽  
N. Metzl ◽  
A. Olsen ◽  
...  
Keyword(s):  
Partial Pressure ◽  
Mixed Layer ◽  
Co2 Flux ◽  
Companion Paper ◽  
Diagnostic Model ◽  
Ocean Mixed Layer ◽  
Co2 Partial Pressure ◽  
Surface Ocean ◽  
Flux Variability ◽  
Global Surface

Abstract. A temporally and spatially resolved estimate of the global surface-ocean CO2 partial pressure field and the sea–air CO2 flux is presented, obtained by fitting a simple data-driven diagnostic model of ocean mixed-layer biogeochemistry to surface-ocean CO2 partial pressure data from the SOCAT v1.5 database. Results include seasonal, interannual, and short-term (daily) variations. In most regions, estimated seasonality is well constrained from the data, and compares well to the widely used monthly climatology by Takahashi et al. (2009). Comparison to independent data tentatively supports the slightly higher seasonal variations in our estimates in some areas. We also fitted the diagnostic model to atmospheric CO2 data. The results of this are less robust, but in those areas where atmospheric signals are not strongly influenced by land flux variability, their seasonality is nevertheless consistent with the results based on surface-ocean data. From a comparison with an independent seasonal climatology of surface-ocean nutrient concentration, the diagnostic model is shown to capture relevant surface-ocean biogeochemical processes reasonably well. Estimated interannual variations will be presented and discussed in a companion paper.

scholarly journals Sea-air CO<sub>2</sub> flux estimated from SOCAT surface-ocean CO<sub>2</sub> partial pressure data and atmospheric CO<sub>2</sub> mixing ratio data

2012 ◽  
Vol 9 (3) ◽  
pp. 2273-2326 ◽  
Author(s):  
C. Rödenbeck ◽  
R. F. Keeling ◽  
D. C. E. Bakker ◽  
N. Metzl ◽  
A. Olsen ◽  
...  
Keyword(s):  
Partial Pressure ◽  
Carbon Sources ◽  
Co2 Flux ◽  
Atmospheric Co2 ◽  
Diagnostic Model ◽  
Pressure Data ◽  
Co2 Partial Pressure ◽  
Sources And Sinks ◽  
Surface Ocean ◽  
Spatio Temporal

Abstract. Surface-ocean CO2 partial pressure data have been assimilated into a simple diagnostic model of surface-ocean biogeochemistry to estimate the spatio-temporal CO2 partial pressure field and ultimately the sea-air CO2 fluxes. Results compare well with the widely used monthly climatology by Takahashi et al. (2009) but also contain some short-term and interannual variations. Fitting the same model to atmospheric CO2 data yields less robust but consistent estimates, confirming that using the partial pressure based estimates as ocean prior in atmospheric CO2 inversions may improve land CO2 flux estimates. Estimated seasonality of ocean-internal carbon sources and sinks is discussed in the light of observed nutrient variations.

scholarly journals Interannual sea–air CO<sub>2</sub> flux variability from an observation-driven ocean mixed-layer scheme

2014 ◽  
Vol 11 (17) ◽  
pp. 4599-4613 ◽  
Author(s):  
C. Rödenbeck ◽  
D. C. E. Bakker ◽  
N. Metzl ◽  
A. Olsen ◽  
C. Sabine ◽  
...  
Keyword(s):  
Southern Oscillation ◽  
Atmospheric Oxygen ◽  
Large Fraction ◽  
Co2 Flux ◽  
Co2 Exchange ◽  
Co2 Partial Pressure ◽  
Surface Ocean ◽  
The North ◽  
Ocean Carbon ◽  
Carbon Dioxide Co2

Abstract. Interannual anomalies in the sea–air carbon dioxide (CO2) exchange have been estimated from surface-ocean CO2 partial pressure measurements. Available data are sufficient to constrain these anomalies in large parts of the tropical and North Pacific and in the North Atlantic, in some areas covering the period from the mid 1980s to 2011. Global interannual variability is estimated as about 0.31 Pg C yr−1 (temporal standard deviation 1993–2008). The tropical Pacific accounts for a large fraction of this global variability, closely tied to El Niño–Southern Oscillation (ENSO). Anomalies occur more than 6 months later in the east than in the west. The estimated amplitude and ENSO response are roughly consistent with independent information from atmospheric oxygen data. This both supports the variability estimated from surface-ocean carbon data and demonstrates the potential of the atmospheric oxygen signal to constrain ocean biogeochemical processes. The ocean variability estimated from surface-ocean carbon data can be used to improve land CO2 flux estimates from atmospheric inversions.

scholarly journals CO<sub>2</sub> partial pressure and CO<sub>2</sub> emission along the lower Red River (Vietnam)

2018 ◽  
Vol 15 (15) ◽  
pp. 4799-4814 ◽  
Author(s):  
Thi Phuong Quynh Le ◽  
Cyril Marchand ◽  
Cuong Tu Ho ◽  
Nhu Da Le ◽  
Thi Thuy Duong ◽  
...  
Keyword(s):  
Partial Pressure ◽  
Co2 Flux ◽  
River System ◽  
Water Quality Monitoring ◽  
Red River ◽  
Wet Season ◽  
Night Time ◽  
Co2 Partial Pressure ◽  
The Difference ◽  
Hoa Binh

Abstract. The Red River (Vietnam) is representative of a south-east Asian river system, strongly affected by climate and human activities. This study aims to quantify the spatial and seasonal variability of CO2 partial pressure and CO2 emissions of the lower Red River system. Water quality monitoring and riverine pCO2 measurements were carried out for 24 h at five stations distributed along the lower Red River system during the dry and the wet seasons. The riverine pCO2 was supersaturated relative to the atmospheric equilibrium (400 ppm), averaging about 1589±43 ppm and resulting in a water–air CO2 flux of 530.3±16.9 mmol m−2 d−1 for the lower Red River. pCO2 and CO2 outgassing rates were characterized by significant spatial variation along this system, with the highest values measured at Hoa Binh station, located downstream of the Hoa Binh Dam, on the Da River. Seasonal pCO2 and CO2 outgassing rate variations were also observed, with higher values measured during the wet season at almost all sites. The higher river discharges, enhanced external inputs of organic matter from watersheds and direct inputs of CO2 from soils or wetland were responsible for higher pCO2 and CO2 outgassing rates. The difference in pCO2 between the daytime and the night-time was not significant, suggesting weak photosynthesis processes in the water column of the Red River due to its high sediment load.

scholarly journals Interannual sea–air CO<sub>2</sub> flux variability from an observation-driven ocean mixed-layer scheme

2014 ◽  
Vol 11 (2) ◽  
pp. 3167-3207 ◽  
Author(s):  
C. Rödenbeck ◽  
D. C. E. Bakker ◽  
N. Metzl ◽  
A. Olsen ◽  
C. Sabine ◽  
...  
Keyword(s):  
Atmospheric Oxygen ◽  
Large Fraction ◽  
Co2 Flux ◽  
Co2 Exchange ◽  
Co2 Partial Pressure ◽  
Surface Ocean ◽  
Independent Information ◽  
Northern Pacific ◽  
Ocean Carbon ◽  
Carbon Dioxide Co2

Abstract. Interannual anomalies in the sea–air carbon dioxide (CO2) exchange have been estimated from surface-ocean CO2 partial pressure measurements. Available data are sufficient to constrain these anomalies in large parts of the tropical and Northern Pacific and in the Northern Atlantic, in some areas since the mid 1980s to 2011. Global interannual variability is estimated as about 0.31 Pg C yr−1 (temporal standard deviation 1993–2008). The tropical Pacific accounts for a large fraction of this global variability, closely tied to ENSO. Anomalies occur more than 6 months later in the East than in the West. The estimated amplitude and ENSO response are consistent with independent information from atmospheric oxygen data. Despite discrepancies in detail, this both supports the variability estimated from surface-ocean carbon data, and demonstrates the potential of the atmospheric oxygen signal to constrain ocean biogeochemical processes. The ocean variability estimated from surface-ocean carbon data can be used to improve land CO2 flux estimates from atmospheric inversions.

scholarly journals Data-based estimates of the ocean carbon sink variability – first results of the Surface Ocean <i>p</i>CO<sub>2</sub> Mapping intercomparison (SOCOM)

2015 ◽  
Vol 12 (23) ◽  
pp. 7251-7278 ◽  
Author(s):  
C. Rödenbeck ◽  
D. C. E. Bakker ◽  
N. Gruber ◽  
Y. Iida ◽  
A. R. Jacobson ◽  
...  
Keyword(s):  
Carbon Sink ◽  
Atmospheric Oxygen ◽  
Co2 Flux ◽  
Process Models ◽  
Global Ocean ◽  
Co2 Uptake ◽  
Co2 Partial Pressure ◽  
Surface Ocean ◽  
Eastern Equatorial Pacific ◽  
Ocean Carbon

Abstract. Using measurements of the surface-ocean CO2 partial pressure (pCO2) and 14 different pCO2 mapping methods recently collated by the Surface Ocean pCO2 Mapping intercomparison (SOCOM) initiative, variations in regional and global sea–air CO2 fluxes are investigated. Though the available mapping methods use widely different approaches, we find relatively consistent estimates of regional pCO2 seasonality, in line with previous estimates. In terms of interannual variability (IAV), all mapping methods estimate the largest variations to occur in the eastern equatorial Pacific. Despite considerable spread in the detailed variations, mapping methods that fit the data more closely also tend to agree more closely with each other in regional averages. Encouragingly, this includes mapping methods belonging to complementary types – taking variability either directly from the pCO2 data or indirectly from driver data via regression. From a weighted ensemble average, we find an IAV amplitude of the global sea–air CO2 flux of 0.31 PgC yr−1 (standard deviation over 1992–2009), which is larger than simulated by biogeochemical process models. From a decadal perspective, the global ocean CO2 uptake is estimated to have gradually increased since about 2000, with little decadal change prior to that. The weighted mean net global ocean CO2 sink estimated by the SOCOM ensemble is −1.75 PgC yr−1 (1992–2009), consistent within uncertainties with estimates from ocean-interior carbon data or atmospheric oxygen trends.

scholarly journals Dark Reduction Drives Evasion of Mercury From the Ocean

2021 ◽  
Vol 2 ◽  
Author(s):  
Carl H. Lamborg ◽  
Colleen M. Hansel ◽  
Katlin L. Bowman ◽  
Bettina M. Voelker ◽  
Ryan M. Marsico ◽  
...  
Keyword(s):  
Mixed Layer ◽  
Surface Waters ◽  
Redox Reactions ◽  
Hydrothermal Vents ◽  
Vertical Mixing ◽  
Reduction Rate ◽  
Elemental Mercury ◽  
Ocean Mixed Layer ◽  
Surface Ocean ◽  
Redox Agents

Much of the surface water of the ocean is supersaturated in elemental mercury (Hg0) with respect to the atmosphere, leading to sea-to-air transfer or evasion. This flux is large, and nearly balances inputs from the atmosphere, rivers and hydrothermal vents. While the photochemical production of Hg0 from ionic and methylated mercury is reasonably well-studied and can produce Hg0 at fairly high rates, there is also abundant Hg0 in aphotic waters, indicating that other important formation pathways exist. Here, we present results of gross reduction rate measurements, depth profiles and diel cycling studies to argue that dark reduction of Hg2+ is also capable of sustaining Hg0 concentrations in the open ocean mixed layer. In locations where vertical mixing is deep enough relative to the vertical penetration of UV-B and photosynthetically active radiation (the principal forms of light involved in abiotic and biotic Hg photoreduction), dark reduction will contribute the majority of Hg0 produced in the surface ocean mixed layer. Our measurements and modeling suggest that these conditions are met nearly everywhere except at high latitudes during local summer. Furthermore, the residence time of Hg0 in the mixed layer with respect to evasion is longer than that of redox, a situation that allows dark reduction-oxidation to effectively set the steady-state ratio of Hg0 to Hg2+ in surface waters. The nature of these dark redox reactions in the ocean was not resolved by this study, but our experiments suggest a likely mechanism or mechanisms involving enzymes and/or important redox agents such as reactive oxygen species and manganese (III).

scholarly journals Data-based estimates of the ocean carbon sink variability – first results of the Surface Ocean <i>p</i>CO<sub>2</sub> Mapping intercomparison (SOCOM)

2015 ◽  
Vol 12 (16) ◽  
pp. 14049-14104 ◽  
Author(s):  
C. Rödenbeck ◽  
D. C. E. Bakker ◽  
N. Gruber ◽  
Y. Iida ◽  
A. R. Jacobson ◽  
...  
Keyword(s):  
Carbon Sink ◽  
Atmospheric Oxygen ◽  
Co2 Flux ◽  
Process Models ◽  
Co2 Uptake ◽  
Co2 Partial Pressure ◽  
Surface Ocean ◽  
Eastern Equatorial Pacific ◽  
First Results ◽  
Ocean Carbon

Abstract. Using measurements of the surface-ocean CO2 partial pressure (pCO2) and 14 different pCO2 mapping methods recently collated by the Surface Ocean pCO2 Mapping intercomparison (SOCOM) initiative, variations in regional and global sea–air CO2 fluxes have been investigated. Though the available mapping methods use widely different approaches, we find relatively consistent estimates of regional pCO2 seasonality, in line with previous estimates. In terms of interannual variability (IAV), all mapping methods estimate the largest variations to occur in the Eastern equatorial Pacific. Despite considerable spead in the detailed variations, mapping methods with closer match to the data also tend to be more consistent with each other. Encouragingly, this includes mapping methods belonging to complementary types – taking variability either directly from the pCO2 data or indirectly from driver data via regression. From a weighted ensemble average, we find an IAV amplitude of the global sea–air CO2 flux of 0.31 PgC yr−1 (standard deviation over 1992–2009), which is larger than simulated by biogeochemical process models. On a decadal perspective, the global CO2 uptake is estimated to have gradually increased since about 2000, with little decadal change prior to 2000. The weighted mean total ocean CO2 sink estimated by the SOCOM ensemble is consistent within uncertainties with estimates from ocean-interior carbon data or atmospheric oxygen trends.

Carbon dioxide permeability of rabbit proximal convoluted tubules

1981 ◽  
Vol 240 (3) ◽  
pp. F231-F244 ◽  
Author(s):  
G. J. Schwartz ◽  
A. M. Weinstein ◽  
R. E. Steele ◽  
J. L. Stephenson ◽  
M. B. Burg
Keyword(s):  
Partial Pressure ◽  
Driving Force ◽  
Co2 Flux ◽  
Hydrogen Ion ◽  
Equivalent Thickness ◽  
Co2 Partial Pressure ◽  
Co2 Diffusion ◽  
Valid Estimate ◽  
Convoluted Tubules ◽  
Proximal Convoluted Tubules

CO2 kinetics were studied under conditions in which CO2 partial pressure and either the bicarbonate or hydrogen ion concentrations were unequal in perfusate and bath. A glass pH microelectrode and microcalorimeter were used to measure pH and total CO2 in perfused and collected fluids. Luminal appearance or disappearance of CO2 was determined from the change in concentrations of CO2 and acidic moieties of the buffers between perfused and collected fluids. The pH was not measurably affected by the tubule processes of metabolism, hydrogen ion secretion, and buffer transport because of relatively high flow rates. Since CO2 appearance and disappearance were directly related to CO2 partial pressure differences across the tubule (r = 0.94), this technique provides a valid estimate of transepithelial CO2 flux in response to the driving force of a CO2 partial pressure difference. From flux per unit of driving force and from estimates of resistances to CO2 diffusion in both internal and external unstirred layers, we obtained a transepithelial CO2 permeability of approximately 10(-4) cm3 . s-1 . cm tubule length-1. This corresponds to a diffusion coefficient through the tubule epithelium about half that through an equivalent thickness of water. We conclude that rabbit proximal convoluted tubules are so highly permeable to CO2 that even if all the filtered bicarbonate were reabsorbed by the generation of CO2 in the lumen, the tubular fluid CO2 partial pressure would exceed that of the peritubular blood by less than 4 mmHg.

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