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

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.

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.


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.


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.


Author(s):  
Arne Johannes Holmin ◽  
Erik A Mousing ◽  
Solfrid S Hjøllo ◽  
Morten D Skogen ◽  
Geir Huse ◽  
...  

Abstract Fisheries independent surveys support science and fisheries assessments but are costly. Evaluating the efficacy of a survey before initiating it could save costs. We used the NORWECOM.E2E model to simulate Northeast Atlantic mackerel and Norwegian spring spawning herring distributions in the Norwegian Sea, and we ran vessel transects in silico to simulate acoustic-trawl surveys. The simulated data were processed using standard survey estimation software and compared to the stock abundances in the ecosystem model. Three existing real surveys were manipulated to demonstrate how the simulation framework can be used to investigate effects of changes in survey timing, direction, and coverage on survey estimates. The method picked up general sources of biases and variance, i.e. that surveys conducted during fish migrations are more vulnerable in terms of bias to timing and changes in survey direction than during more stationary situations and that increased effort reduced the sampling variance.


2020 ◽  
Vol 71 (3) ◽  
pp. 263 ◽  
Author(s):  
Catriona L. Hurd ◽  
John Beardall ◽  
Steeve Comeau ◽  
Christopher E. Cornwall ◽  
Jonathan N Havenhand ◽  
...  

‘Multiple drivers’ (also termed ‘multiple stressors’) is the term used to describe the cumulative effects of multiple environmental factors on organisms or ecosystems. Here, we consider ocean acidification as a multiple driver because many inorganic carbon parameters are changing simultaneously, including total dissolved inorganic carbon, CO2, HCO3–, CO32–, H+ and CaCO3 saturation state. With the rapid expansion of ocean acidification research has come a greater understanding of the complexity and intricacies of how these simultaneous changes to the seawater carbonate system are affecting marine life. We start by clarifying key terms used by chemists and biologists to describe the changing seawater inorganic carbon system. Then, using key groups of non-calcifying (fish, seaweeds, diatoms) and calcifying (coralline algae, coccolithophores, corals, molluscs) organisms, we consider how various physiological processes are affected by different components of the carbonate system.


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