scholarly journals Seasonal variability in the inorganic ocean carbon cycle in the Northwest Pacific evaluated using a biogeochemical and carbon model coupled with an operational ocean model

2020 ◽  
Vol 162 (2) ◽  
pp. 877-902
Author(s):  
Miho Ishizu ◽  
Yasumasa Miyazawa ◽  
Tomohiko Tsunoda ◽  
Xinyu Guo

Abstract Here, we investigate the seasonal variability in the dissolved inorganic carbon (DIC) cycle in the Northwest Pacific using a high-resolution biogeochemical and carbon model coupled with an operational ocean model. Results show that the contribution to DIC from air–sea CO2 exchange is generally offset by vertical mixing at the surface at all latitudes, with some seasonal variation. Biological processes in subarctic regions are evident at the surface, whereas in the subtropical region these processes take place within the euphotic layer and then DIC consumption deepens southward with latitude. Such latitudinal differences in biological processes lead to marked horizontal and vertical contrasts in the distribution of DIC, with modulation by horizontal and vertical advection–diffusion processes.

2021 ◽  
Author(s):  
Miho Ishizu ◽  
Yasumasa Miyazawa ◽  
Xinyu Guo

Abstract The multi-decadal variation in ocean acidification indices in the Northwest Pacific was examined using a biogeochemical model with an operational ocean model product for the period 1993–2018. We found that ocean acidification varied regionally in the Northwest Pacific. The surface ocean (above 100 m depth) underwent acidification that progressed more quickly in the subtropical region and the Kuroshio extension than in the subarctic region due to vertical mixing of the dissolved inorganic carbon (DIC) supply exceeding DIC release by air–sea exchange. Below 100 m depth, acidification and alkalinization occurred in the subtropical and subarctic regions, respectively. We attribute these regional differences in acidification and alkalinization to spatially variable biological processes in the upper layer and physical redistribution of DIC, both horizontally and vertically.


Radiocarbon ◽  
1996 ◽  
Vol 38 (3) ◽  
pp. 583-595 ◽  
Author(s):  
Makio C. Honda

In order to verify sediment trap samples as indicators of upper ocean 14C concentrations, particulate inorganic radiocarbon (PICΔ14C) collected by time-series sediment traps in the Sea of Okhotsk and the Bering Sea was measured by accelerator mass spectrometry (AMS). All of the PICΔ14C measurements were < 0‰, in contrast to GEOSECS 14C data in the upper ocean from the northwestern North Pacific. This difference is attributed to the upwelling of deepwater that contains low Δ14C of dissolved inorganic carbon (DICΔ14C) and to the decrease over time of surface DICΔ14C owing to the decrease of atmospheric Δ14C values. In addition, PICΔ14C values showed significant seasonal variability: PICΔ14C collected in the fall was the greatest (-22‰ on average), whereas PICΔ14C collected in winter showed an average minimum of −48‰. It is likely that this difference was caused by changes in mixed layer thickness. Although some uncertainties remain, further study on PICΔ14C will enable us to estimate seasonal variability in DICΔ14C and air-sea CO2 exchange rate.


2019 ◽  
Vol 11 (9) ◽  
pp. 2677 ◽  
Author(s):  
Miho Ishizu ◽  
Yasumasa Miyazawa ◽  
Tomohiko Tsunoda ◽  
Xinyu Guo

We developed a biogeochemical and carbon model (JCOPE_EC) coupled with an operational ocean model for the North Western Pacific. JCOPE_EC represents ocean acidification indices on the background of the risks due to ocean acidification and our model experiences. It is an off-line tracer model driven by a high-resolution regional ocean general circulation model (JCOPE2M). The results showed that the model adequately reproduced the general patterns in the observed data, including the seasonal variability of chlorophyll-a, dissolved inorganic nitrogen/phosphorus, dissolved inorganic carbon, and total alkalinity. We provide an overview of this system and the results of the model validation based on the available observed data. Sensitivity analysis using fixed values for temperature, salinity, dissolved inorganic carbon and total alkalinity helped us identify which variables contributed most to seasonal variations in the ocean acidification indices, pH and Ωarg. The seasonal variation in the pHinsitu was governed mainly by balances of the change in temperature and dissolved inorganic carbon. The seasonal increase in Ωarg from winter to summer was governed mainly by dissolved inorganic carbon levels.


2014 ◽  
Vol 11 (11) ◽  
pp. 15399-15433
Author(s):  
E. Jeansson ◽  
R. G. J. Bellerby ◽  
I. Skjelvan ◽  
H. Frigstad ◽  
S. R. Ólafsdóttir ◽  
...  

Abstract. Fluxes of carbon and nutrients to the upper 100 m of the Iceland Sea are evaluated. The study utilises hydro-chemical data from the Iceland Sea time-series station (68.00° N, 12.67° W), for the years between 1993 and 2006. By comparing data of dissolved inorganic carbon (DIC) and nutrients in the surface layer (upper 100 m), and a sub-surface layer (100–200 m), we calculate monthly deficits in the surface, and use these to deduce the surface layer fluxes that affect the deficits: vertical mixing, horizontal advection, air–sea exchange, and biological activity. The deficits show a clear seasonality with a minimum in winter, when the mixed layer is at the deepest, and a maximum in early autumn, when biological uptake has removed much of the nutrients. The annual vertical fluxes of DIC and nitrate amounts to 1.7 ± 0.3 and 0.23 ± 0.07 mol m−2 yr−1, respectively, and the annual air–sea uptake of atmospheric CO2 is 4.4 ± 1.1 mol m−2 yr−1. The biologically driven changes in DIC during the year relates to net community production (NCP), and the net annual NCP corresponds to export production, and is here calculated to 6.1 ± 0.9 mol C m−2 yr−1. The typical, median C : N ratio during the period of net community uptake is 11, and thus clearly higher than Redfield, but is varying during the season.


Radiocarbon ◽  
1997 ◽  
Vol 40 (2) ◽  
pp. 933-944 ◽  
Author(s):  
Toshio Nakamura ◽  
Sadao Kojima ◽  
Tomoko Ohta ◽  
Hirotaka Oda ◽  
Akiko Ikeda ◽  
...  

This paper reports on concentrations and carbon isotopic results of dissolved inorganic carbon (DIC) in water samples collected at four locations and from several depths in Lake Biwa, central Japan, covering every season of the year, starting in the spring of 1995. Depth profiles of DIC concentration and DIC δ13C showed a strong seasonal pattern, as a result of vertical mixing of the lake water in winter and early spring, or lack of mixing in the other seasons. No seasonal change in DIC ∆14C depth profiles was recognizable, mainly owing to the wide scatter of DIC ∆14C. Values typically ranged from 0.47 to 0.65 mmol kg-1 for DIC concentration, and from -4 to -8‰ and from +10 to +80‰ for DIC ∆13C and DIC ∆14C, respectively, for the Lake Biwa water.


2021 ◽  
Vol 13 (12) ◽  
pp. 5565-5589
Author(s):  
Siv K. Lauvset ◽  
Nico Lange ◽  
Toste Tanhua ◽  
Henry C. Bittig ◽  
Are Olsen ◽  
...  

Abstract. The Global Ocean Data Analysis Project (GLODAP) is a synthesis effort providing regular compilations of surface-to-bottom ocean biogeochemical bottle data, with an emphasis on seawater inorganic carbon chemistry and related variables determined through chemical analysis of seawater samples. GLODAPv2.2021 is an update of the previous version, GLODAPv2.2020 (Olsen et al., 2020). The major changes are as follows: data from 43 new cruises were added, data coverage was extended until 2020, all data with missing temperatures were removed, and a digital object identifier (DOI) was included for each cruise in the product files. In addition, a number of minor corrections to GLODAPv2.2020 data were performed. GLODAPv2.2021 includes measurements from more than 1.3 million water samples from the global oceans collected on 989 cruises. The data for the 12 GLODAP core variables (salinity, oxygen, nitrate, silicate, phosphate, dissolved inorganic carbon, total alkalinity, pH, CFC-11, CFC-12, CFC-113, and CCl4) have undergone extensive quality control with a focus on systematic evaluation of bias. The data are available in two formats: (i) as submitted by the data originator but updated to World Ocean Circulation Experiment (WOCE) exchange format and (ii) as a merged data product with adjustments applied to minimize bias. For this annual update, adjustments for the 43 new cruises were derived by comparing those data with the data from the 946 quality controlled cruises in the GLODAPv2.2020 data product using crossover analysis. Comparisons to estimates of nutrients and ocean CO2 chemistry based on empirical algorithms provided additional context for adjustment decisions in this version. The adjustments are intended to remove potential biases from errors related to measurement, calibration, and data handling practices without removing known or likely time trends or variations in the variables evaluated. The compiled and adjusted data product is believed to be consistent with to better than 0.005 in salinity, 1 % in oxygen, 2 % in nitrate, 2 % in silicate, 2 % in phosphate, 4 µmol kg−1 in dissolved inorganic carbon, 4 µmol kg−1 in total alkalinity, 0.01–0.02 in pH (depending on region), and 5 % in the halogenated transient tracers. The other variables included in the compilation, such as isotopic tracers and discrete CO2 fugacity (fCO2), were not subjected to bias comparison or adjustments. The original data, their documentation, and DOI codes are available at the Ocean Carbon Data System of NOAA NCEI (https://www.ncei.noaa.gov/access/ocean-carbon-data-system/oceans/GLODAPv2_2021/, last access: 7 July 2021). This site also provides access to the merged data product, which is provided as a single global file and as four regional ones – the Arctic, Atlantic, Indian, and Pacific oceans – under https://doi.org/10.25921/ttgq-n825 (Lauvset et al., 2021). These bias-adjusted product files also include significant ancillary and approximated data and can be accessed via https://www.glodap.info (last access: 29 June 2021). These were obtained by interpolation of, or calculation from, measured data. This living data update documents the GLODAPv2.2021 methods and provides a broad overview of the secondary quality control procedures and results.


2020 ◽  
Vol 7 ◽  
Author(s):  
Katharina Seelmann ◽  
Tobias Steinhoff ◽  
Steffen Aßmann ◽  
Arne Körtzinger

Over recent decades, observations based on merchant vessels (Ships of Opportunity—SOOP) equipped with sensors measuring the CO2 partial pressure (pCO2) in the surface seawater formed the backbone of the global ocean carbon observation system. However, the restriction to pCO2 measurements alone is one severe shortcoming of the current SOOP observatory. Full insight into the marine inorganic carbon system requires the measurement of at least two of the four measurable variables which are pCO2, total alkalinity (TA), dissolved inorganic carbon (DIC), and pH. One workaround is to estimate TA values based on established temperature-salinity parameterizations, but this leads to higher uncertainties and the possibility of regional and/or seasonal biases. Therefore, autonomous SOOP-based TA measurements are of great interest. Our study describes the implementation of a novel autonomous analyzer for seawater TA, the CONTROS HydroFIAⓇ TA system (-4H-JENA engineering GmbH, Germany) for unattended routine TA measurements on a SOOP line operating in the North Atlantic. We present the installation in detail and address major issues encountered with autonomous measurements using this analyzer, e.g., automated cleaning and stabilization routines, and waste handling. Another issue during long-term deployments is the provision of reference seawater in large-volume containers for quality assurance measurements and drift correction. Hence, a stable large-volume seawater storage had to be found. We tested several container types with respect to their suitability to store seawater over a time period of 30 days without significant changes in TA. Only one gas sampling bag made of polyvinylidene fluoride (PVDF) satisfied the high stability requirement. In order to prove the performance of the entire setup, we compared the autonomous TA measurements with TA from discrete samples taken during the first two trans-Atlantic crossings. Although the measurement accuracy in unattended mode (about ± 5 μmol kg^-1) slightly deteriorated compared to our previous system characterization, its overall uncertainty fulfilled requirements for autonomous TA measurements on SOOP lines. A comparison with predicted TA values based on an established and often used parameterization pointed at regional and seasonal limitations of such TA predictions. Consequently, TA observations with better coverage of spatiotemporal variability are needed, which is now possible with the method described here.


2011 ◽  
Vol 124 (1-4) ◽  
pp. 23-37 ◽  
Author(s):  
E.H. Shadwick ◽  
H. Thomas ◽  
K. Azetsu-Scott ◽  
B.J.W. Greenan ◽  
E. Head ◽  
...  

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