scholarly journals Carbon and nutrient mixed layer dynamics in the Norwegian Sea

2008 ◽  
Vol 5 (5) ◽  
pp. 1395-1410 ◽  
Author(s):  
H. S. Findlay ◽  
T. Tyrrell ◽  
R. G. J. Bellerby ◽  
A. Merico ◽  
I. Skjelvan

Abstract. A coupled carbon-ecosystem model is compared to recent data from Ocean Weather Station M (66° N, 02° E) and used as a tool to investigate nutrient and carbon processes within the Norwegian Sea. Nitrate is consumed by phytoplankton in the surface layers over the summer; however the data show that silicate does not become rapidly limiting for diatoms, in contrast to the model prediction and in contrast to data from other temperate locations. The model estimates atmosphere-ocean CO2 flux to be 37 g C m−2 yr−1. The seasonal cycle of the carbonate system at OWS M resembles the cycles suggested by data from other high-latitude ocean locations. The seasonal cycles of calcite saturation state and [CO32-] are similar in the model and in data at OWS M: values range from ~3 and ~120 μmol kg−1 respectively in winter, to ~4 and ~170 μmol kg−1 respectively in summer. The model and data provide further evidence (supporting previous modelling work) that the summer is a time of high saturation state within the annual cycle at high-latitude locations. This is also the time of year that coccolithophore blooms occur at high latitudes.

2007 ◽  
Vol 4 (5) ◽  
pp. 3229-3265 ◽  
Author(s):  
H. S. Findlay ◽  
T. Tyrrell ◽  
R. G. J. Bellerby ◽  
A. Merico ◽  
I. Skjelvan

Abstract. A coupled carbon-ecosystem model is compared to recent data from Ocean Weather Ship M (66° N, 02° E) and used to investigate nutrient and carbon processes within the Norwegian Sea. Nitrate is consumed by phytoplankton in the surface layers over the summer; however the data show that silicate does not become rapidly limiting for diatoms, in contrast to the model prediction and in contrast to data from other temperate locations. The model estimates atmosphere-ocean CO2 flux to be 37 g C m−2 yr−1. A detailed comparison of the carbonate system at other ocean locations reveals that although coccolithophore blooms occur at OWS M, they are not as prevalent here as other areas. The seasonal cycles of calcite saturation state and [CO32−] are similar in the model and in data: values range from ~3 and ~120 μmol kg−1 respectively in winter, to ~4 and ~170 μmol kg−1 respectively in summer. The timing of coccolithophore blooms within the year therefore coincides with a time of high calcite saturation state, as predicted by previous modelling work.


2012 ◽  
Vol 9 (2) ◽  
pp. 1781-1792 ◽  
Author(s):  
C. J. M. Hoppe ◽  
G. Langer ◽  
S. D. Rokitta ◽  
D. A. Wolf-Gladrow ◽  
B. Rost

Abstract. The growing field of ocean acidification research is concerned with the investigation of organisms' responses to increasing pCO2 values. One important approach in this context is culture work using seawater with adjusted CO2 levels. As aqueous pCO2 is difficult to measure directly in small scale experiments, it is generally calculated from two other measured parameters of the carbonate system (often AT, CT or pH). Unfortunately, the overall uncertainties of measured and subsequently calculated values are often unknown. Especially under high pCO2, this can become a severe problem with respect to the interpretation of physiological and ecological data. In the few datasets from ocean acidification research where all three of these parameters were measured, pCO2 values calculated from AT and CT are typically about 30 % lower (i.e. ~300 μatm at a target pCO2 of 1000 μatm) than those calculated from AT and pH or CT and pH. This study presents and discusses these discrepancies as well as likely consequences for the ocean acidification community. Until this problem is solved, one has to consider that calculated parameters of the carbonate system (e.g. pCO2, calcite saturation state) may not be comparable between studies, and that this may have important implications for the interpretation of CO2 perturbation experiments.


2012 ◽  
Vol 9 (7) ◽  
pp. 2401-2405 ◽  
Author(s):  
C. J. M. Hoppe ◽  
G. Langer ◽  
S. D. Rokitta ◽  
D. A. Wolf-Gladrow ◽  
B. Rost

Abstract. The growing field of ocean acidification research is concerned with the investigation of organism responses to increasing pCO2 values. One important approach in this context is culture work using seawater with adjusted CO2 levels. As aqueous pCO2 is difficult to measure directly in small-scale experiments, it is generally calculated from two other measured parameters of the carbonate system (often AT, CT or pH). Unfortunately, the overall uncertainties of measured and subsequently calculated values are often unknown. Especially under high pCO2, this can become a severe problem with respect to the interpretation of physiological and ecological data. In the few datasets from ocean acidification research where all three of these parameters were measured, pCO2 values calculated from AT and CT are typically about 30% lower (i.e. ~300 μatm at a target pCO2 of 1000 μatm) than those calculated from AT and pH or CT and pH. This study presents and discusses these discrepancies as well as likely consequences for the ocean acidification community. Until this problem is solved, one has to consider that calculated parameters of the carbonate system (e.g. pCO2, calcite saturation state) may not be comparable between studies, and that this may have important implications for the interpretation of CO2 perturbation experiments.


2021 ◽  
Vol 21 (22) ◽  
pp. 16661-16687
Author(s):  
Nicole Jacobs ◽  
William R. Simpson ◽  
Kelly A. Graham ◽  
Christopher Holmes ◽  
Frank Hase ◽  
...  

Abstract. Satellite-based observations of atmospheric carbon dioxide (CO2) provide measurements in remote regions, such as the biologically sensitive but undersampled northern high latitudes, and are progressing toward true global data coverage. Recent improvements in satellite retrievals of total column-averaged dry air mole fractions of CO2 (XCO2) from the NASA Orbiting Carbon Observatory 2 (OCO-2) have allowed for unprecedented data coverage of northern high-latitude regions, while maintaining acceptable accuracy and consistency relative to ground-based observations, and finally providing sufficient data in spring and autumn for analysis of satellite-observed XCO2 seasonal cycles across a majority of terrestrial northern high-latitude regions. Here, we present an analysis of XCO2 seasonal cycles calculated from OCO-2 data for temperate, boreal, and tundra regions, subdivided into 5∘ latitude by 20∘ longitude zones. We quantify the seasonal cycle amplitudes (SCAs) and the annual half drawdown day (HDD). OCO-2 SCAs are in good agreement with ground-based observations at five high-latitude sites, and OCO-2 SCAs show very close agreement with SCAs calculated for model estimates of XCO2 from the Copernicus Atmosphere Monitoring Services (CAMS) global inversion-optimized greenhouse gas flux model v19r1 and the CarbonTracker2019 model (CT2019B). Model estimates of XCO2 from the GEOS-Chem CO2 simulation version 12.7.2 with underlying biospheric fluxes from CarbonTracker2019 (GC-CT2019) yield SCAs of larger magnitude and spread over a larger range than those from CAMS, CT2019B, or OCO-2; however, GC-CT2019 SCAs still exhibit a very similar spatial distribution across northern high-latitude regions to that from CAMS, CT2019B, and OCO-2. Zones in the Asian boreal forest were found to have exceptionally large SCA and early HDD, and both OCO-2 data and model estimates yield a distinct longitudinal gradient of increasing SCA from west to east across the Eurasian continent. In northern high-latitude regions, spanning latitudes from 47 to 72∘ N, longitudinal gradients in both SCA and HDD are at least as pronounced as latitudinal gradients, suggesting a role for global atmospheric transport patterns in defining spatial distributions of XCO2 seasonality across these regions. GEOS-Chem surface contact tracers show that the largest XCO2 SCAs occur in areas with the greatest contact with land surfaces, integrated over 15–30 d. The correlation of XCO2 SCA with these land surface contact tracers is stronger than the correlation of XCO2 SCA with the SCA of CO2 fluxes or the total annual CO2 flux within each 5∘ latitude by 20∘ longitude zone. This indicates that accumulation of terrestrial CO2 flux during atmospheric transport is a major driver of regional variations in XCO2 SCA.


2021 ◽  
Author(s):  
Nicole Jacobs ◽  
William R. Simpson ◽  
Kelly A. Graham ◽  
Christopher Holmes ◽  
Frank Hase ◽  
...  

Abstract. Satellite-based observations of atmospheric carbon dioxide (CO2) provide measurements in remote regions, such as the biologically sensitive but under sampled northern high latitudes, and are progressing toward true global data coverage. Recent improvements in satellite retrievals of total column-averaged dry air mole fractions of CO2 (XCO2) from the NASA Orbiting Carbon Observatory 2 (OCO-2) have allowed for unprecedented data coverage of northern high latitude regions, while maintaining acceptable accuracy and consistency relative to ground-based observations, and finally providing sufficient data in spring and autumn for analysis of the satellite-observed XCO2 seasonal cycles across a majority of terrestrial northern high latitude regions. Here, we present an analysis of XCO2 seasonal cycles calculated from OCO-2 data for temperate, boreal, and tundra regions, subdivided into 5° latitude by 20° longitude zones. We quantify the seasonal cycle amplitudes (SCA) and the annual half drawdown day (HDD). OCO-2 SCA is in good agreement with ground-based observations at five high latitude sites and OCO-2 SCA show very close agreement with SCA calculated for model estimates of XCO2 from the Copernicus Atmospheric Monitoring Services (CAMS) global inversion-optimized greenhouse gas flux model v19r1. Model estimates of XCO2 from the GEOS-Chem CO2 simulation version 12.7.2 with underlying biospheric fluxes from CarbonTracker2019 yield SCA of larger magnitude and spread over a larger range than those from CAMS and OCO-2; however, GEOS-Chem SCA still exhibit a very similar spatial distribution across northern high latitude regions to that from CAMS and OCO-2. Zones in the Asian Boreal Forest were found to have exceptionally large SCA and early HDD, and both OCO-2 data and model estimates yield a distinct longitudinal gradient of increasing SCA from west to east across the Eurasian continent. Longitudinal gradients in both SCA and HDD are at least as pronounced as meridional gradients (with respect to latitude), suggesting an essential role for global atmospheric transport patterns in defining XCO2 seasonality. GEOS-Chem surface contact tracers show that the largest XCO2 SCA occurs in areas with the greatest contact with land surfaces, integrated over 15–30 days. The correlation of XCO2 SCA with these land contact tracers are stronger than the correlation of XCO2 SCA with the SCA of CO2 fluxes within each 5° latitude by 20° longitude zone. This indicates that accumulation of terrestrial CO2 flux during atmospheric transport is a major driver of regional variations in XCO2 SCA.


2014 ◽  
Vol 11 (24) ◽  
pp. 7349-7362 ◽  
Author(s):  
B. R. Carter ◽  
J. R. Toggweiler ◽  
R. M. Key ◽  
J. L. Sarmiento

Abstract. We introduce a composite tracer for the marine system, Alk*, that has a global distribution primarily determined by CaCO3 precipitation and dissolution. Alk* is also affected by riverine alkalinity from dissolved terrestrial carbonate minerals. We estimate that the Arctic receives approximately twice the riverine alkalinity per unit area as the Atlantic, and 8 times that of the other oceans. Riverine inputs broadly elevate Alk* in the Arctic surface and particularly near river mouths. Strong net carbonate precipitation results in low Alk* in subtropical gyres, especially in the Indian and Atlantic oceans. Upwelling of dissolved CaCO3-rich deep water elevates North Pacific and Southern Ocean Alk*. We use the Alk* distribution to estimate the variability of the calcite saturation state resulting from CaCO3 cycling and other processes. We show that regional differences in surface calcite saturation state are due primarily to the effect of temperature differences on CO2 solubility and, to a lesser extent, differences in freshwater content and air–sea disequilibria. The variations in net calcium carbonate cycling revealed by Alk* play a comparatively minor role in determining the calcium carbonate saturation state.


2014 ◽  
Vol 11 (3) ◽  
pp. 4531-4561 ◽  
Author(s):  
J. R. Young ◽  
A. J. Poulton ◽  
T. Tyrrell

Abstract. Within the context of the UK Ocean Acidification project, Emiliania huxleyi (type A) coccolith morphology was examined from samples collected during cruise D366. In particular, a morphometric study of coccolith size and degree of calcification was made on scanning electron microscope images of samples from shipboard CO2 perturbation experiments and from a set of environmental samples with significant variation in calcite saturation state (Ωcalcite). One bioassay in particular (E4 from the southern North Sea) yielded unambiguous results – in this bioassay exponential growth from a low level occurred with no artificial stimulation and coccosphere numbers increased ten-fold during the experiment. The samples with elevated CO2 saw significantly reduced coccolithophore growth. However, coccolithophore morphology was not significantly affected by the changing CO2 conditions even under the highest levels of perturbation (1000 μatm). Environmental samples similarly showed no correlation of coccolithophore morphology with calcite saturation state. Some variation in coccolith size and degree of calcification does occur but this seems to be predominantly due to genotypic differentiation between populations on the shelf and in the open ocean.


2007 ◽  
Vol 246 (2-4) ◽  
pp. 68-85 ◽  
Author(s):  
Jan Sverre Laberg ◽  
Stephanie Guidard ◽  
Jürgen Mienert ◽  
Tore O. Vorren ◽  
Haflidi Haflidason ◽  
...  
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