scholarly journals Does ocean acidification induce an upward flux of marine aggregates?

2008 ◽  
Vol 5 (4) ◽  
pp. 1023-1031 ◽  
Author(s):  
X. Mari
Keyword(s):  
Ocean Acidification ◽  
Atmospheric Carbon Dioxide ◽  
New Caledonia ◽  
Seawater Acidification ◽  
Seawater Ph ◽  
Biogenic Carbon ◽  
Marine Aggregates ◽  
Atmospheric Carbon ◽  
Carbon Dioxide Co2 ◽  
Sedimentation Processes

Abstract. The absorption of anthropogenic atmospheric carbon dioxide (CO2) by the ocean provokes its acidification. This acidification may alter several oceanic processes, including the export of biogenic carbon from the upper layer of the ocean, hence providing a feedback on rising atmospheric carbon concentrations. The effect of seawater acidification on transparent exopolymeric particles (TEP) driven aggregation and sedimentation processes were investigated by studying the interactions between latex beads and TEP precursors collected in the lagoon of New Caledonia. A suspension of TEP and beads was prepared and the formation of mixed aggregates was monitored as a function of pH under increasing turbulence intensities. The pH was controlled by addition of sulfuric acid. Aggregation and sedimentation processes driven by TEP were drastically reduced when the pH of seawater decreases within the expected limits imposed by increased anthropogenic CO2 emissions. In addition to the diminution of TEP sticking properties, the diminution of seawater pH led to a significant increase of the TEP pool, most likely due to swollen structures. A diminution of seawater pH by 0.2 units or more led to a stop or a reversal of the downward flux of particles. If applicable to oceanic conditions, the sedimentation of marine aggregates may slow down or even stop as the pH decreases, and the vertical flux of organic carbon may reverse. This would enhance both rising atmospheric carbon and ocean acidification.

scholarly journals Does ocean acidification induce an upward flux of marine aggregates?

2008 ◽  
Vol 5 (2) ◽  
pp. 1631-1654 ◽  
Author(s):  
X. Mari
Keyword(s):  
Ocean Acidification ◽  
Atmospheric Carbon Dioxide ◽  
New Caledonia ◽  
Seawater Acidification ◽  
Seawater Ph ◽  
Biogenic Carbon ◽  
Marine Aggregates ◽  
Atmospheric Carbon ◽  
Carbon Dioxide Co2 ◽  
Sedimentation Processes

Abstract. The adsorption of anthropogenic atmospheric carbon dioxide (CO2) by the ocean provokes its acidification. This acidification may alter several oceanic processes, including the export of biogenic carbon from the upper layer of the ocean, hence providing a feedback on rising atmospheric carbon concentrations. The effect of seawater acidification on transparent exopolymeric particles (TEP) driven aggregation and sedimentation processes were investigated by studying the interactions between latex beads and TEP precursors collected in the lagoon of New Caledonia. A suspension of TEP and beads was prepared and the formation of mixed aggregates was monitored as a function of pH under increasing turbulence intensities. The pH was controlled by addition of sulfuric acid. Aggregation and sedimentation processes driven by TEP were drastically reduced when the pH of seawater decreases within the expected limits imposed by increased anthropogenic CO2 emissions. In addition to the diminution of TEP sticking properties, the diminution of seawater pH led to a significant increase of the TEP pool, most likely due to swollen structures. A diminution of seawater pH by 0.2 units or more led to a stop or a reversal of the downward flux of particles. If applicable to oceanic conditions, the sedimentation of marine aggregates may slow down or even stop as the pH decreases, and the vertical flux of organic carbon may reverse. This would enhance both rising atmospheric carbon and ocean acidification.

scholarly journals Using airborne HIAPER Pole-to-Pole Observations (HIPPO) to evaluate model and remote sensing estimates of atmospheric carbon dioxide

2016 ◽  
Author(s):  
C. Frankenberg ◽  
S. S. Kulawik ◽  
S. Wofsy ◽  
F. Chevallier ◽  
B. Daube ◽  
...  
Keyword(s):  
Carbon Dioxide ◽  
Atmospheric Carbon Dioxide ◽  
Correlation Coefficients ◽  
Added Value ◽  
Total Carbon ◽  
Accuracy And Precision ◽  
Atmospheric Carbon ◽  
Carbon Dioxide Co2 ◽  
Global Carbon ◽  
Comparable Quality

Abstract. In recent years, space-borne observations of atmospheric carbon-dioxide (CO2) have become increasingly used in global carbon-cycle studies. In order to obtain added value from space-borne measurements, they have to suffice stringent accuracy and precision requirements, with the latter being less crucial as it can be reduced by just enhanced sample size. Validation of CO2 column averaged dry air mole fractions (XCO2) heavily relies on measurements of the Total Carbon Column Observing Network TCCON. Owing to the sparseness of the network and the requirements imposed on space-based measurements, independent additional validation is highly valuable. Here, we use observations from the HIAPER Pole-to-Pole Observations (HIPPO) flights from January 2009 through September 2011 to validate CO2 measurements from satellites (GOSAT, TES, AIRS) and atmospheric inversion models (CarbonTracker CT2013B, MACC v13r1). We find that the atmospheric models capture the XCO2 variability observed in HIPPO flights very well, with correlation coefficients (r2) of 0.93 and 0.95 for CT2013B and MACC, respectively. Some larger discrepancies can be observed in profile comparisons at higher latitudes, esp. at 300 hPa during the peaks of either carbon uptake or release. These deviations can be up to 4 ppm and hint at misrepresentation of vertical transport. Comparisons with the GOSAT satellite are of comparable quality, with an r2 of 0.85, a mean bias μ of −0.06 ppm and a standard deviation σ of 0.45 ppm. TES exhibits an r2 of 0.75, μ of 0.34 ppm and σ of 1.13 ppm. For AIRS, we find an r2 of 0.37, μ of 1.11 ppm and σ of 1.46 ppm, with latitude-dependent biases. For these comparisons at least 6, 20 and 50 atmospheric soundings have been averaged for GOSAT, TES and AIRS, respectively. Overall, we find that GOSAT soundings over the remote pacific ocean mostly meet the stringent accuracy requirements of about 0.5 ppm for space-based CO2 observations.

scholarly journals Effect of elevated CO<sub>2</sub> on the dynamics of particle attached and free living bacterioplankton communities in an Arctic fjord

2012 ◽  
Vol 9 (8) ◽  
pp. 10725-10755 ◽  
Author(s):  
M. Sperling ◽  
J. Piontek ◽  
G. Gerdts ◽  
A. Wichels ◽  
H. Schunck ◽  
...  
Keyword(s):  
Ocean Acidification ◽  
Atmospheric Carbon Dioxide ◽  
Intergenic Spacer ◽  
Extracellular Enzyme ◽  
The Arctic ◽  
Organic Substrates ◽  
Viral Lysis ◽  
Free Living ◽  
High Co2 ◽  
Carbon Dioxide Co2

Abstract. The increase in atmospheric carbon dioxide (CO2) results in acidification of the oceans, expected to lead to the fastest drop in ocean pH in the last 300 million years, if anthropogenic emissions are continued at present rate. Due to higher solubility of gases in cold waters and increased exposure to the atmosphere by decreasing ice cover, the Arctic Ocean will be among the areas most strongly affected by ocean acidification. Yet, the response of the plankton community of high latitudes to ocean acidification has not been studied so far. This work is part of the Arctic campaign of the European Project on Ocean Acidification (EPOCA) in 2010, employing 9 in situ mesocosms of about 45 000 l each to simulate ocean acidification in Kongsfjorden, Svalbard (78°56.2' N 11°53.6' E). In the present study, we investigated effects of elevated CO2 on the composition and richness of particle attached (PA; >3 μm) and free living (FL; <3 μm >0.2 μm) bacterial communities by Automated Ribosomal Intergenic Spacer Analysis (ARISA) in 6 of the mesocosms and the surrounding fjord, ranging from 185 to 1050 initial μatm pCO2. ARISA was able to resolve about 20–30 bacterial band-classes per sample and allowed for a detailed investigation of the explicit richness. Both, the PA and the FL bacterioplankton community exhibited a strong temporal development, which was driven mainly by temperature and phytoplankton development. In response to the breakdown of a picophytoplankton bloom (phase 3 of the experiment), number of ARISA-band classes in the PA-community were reduced at low and medium CO2 (∼180–600 μatm) by about 25%, while it was more or less stable at high CO2 (∼ 650–800 μatm). We hypothesise that enhanced viral lysis and enhanced availability of organic substrates at high CO2 resulted in a more diverse PA-bacterial community in the post-bloom phase. Despite lower cell numbers and extracellular enzyme activities in the post-bloom phase, bacterial protein production was enhanced in high CO2-treatments, suggesting a positive effect of community richness on this function and on carbon cycling by bacteria.

scholarly journals Development and field testing of a rapid and ultra-stable atmospheric carbon dioxide spectrometer

2014 ◽  
Vol 7 (8) ◽  
pp. 8101-8123
Author(s):  
B. Xiang ◽  
D. D. Nelson ◽  
J. B. McManus ◽  
M. S. Zahniser ◽  
R. Wehr ◽  
...  
Keyword(s):  
Carbon Dioxide ◽  
Field Test ◽  
Atmospheric Carbon Dioxide ◽  
Field Measurements ◽  
Field Testing ◽  
Thermal Control ◽  
Long Term Ecological Research ◽  
Calibration Protocol ◽  
Atmospheric Carbon ◽  
Carbon Dioxide Co2

Abstract. We present field test results for a new spectroscopic instrument to measure atmospheric carbon dioxide (CO2) with high precision (0.02 ppm at 1 Hz) and demonstrate high stability (within 0.1 ppm over more than 8 months), without the need for hourly, daily, or even monthly calibration against high-pressure gas cylinders. The technical novelty of this instrument (ABsolute Carbon dioxide, ABC) is the spectral null method using an internal quartz reference cell with known CO2 column density. Compared to a previously described prototype, the field instrument has better stability and benefits from more precise thermal control of the optics and more accurate pressure measurements in the sample cell (at the mTorr level). The instrument has been deployed at a long-term ecological research site (the Harvard Forest, USA), where it has measured for eight months without on-site calibration and with minimal maintenance, showing drift bounds of less than 0.1 ppm. Field measurements agree well with those of another commercially available cavity ring-down CO2 instrument (Picarro G2301) run with a standard calibration protocol. This field test demonstrates that ABC is capable of performing high-accuracy, unattended, continuous field measurements with minimal use of calibration cylinders.

scholarly journals Progressive seawater acidification on the Great Barrier Reef continental shelf

2020 ◽  
Vol 10 (1) ◽  
Author(s):  
Katharina E. Fabricius ◽  
Craig Neill ◽  
Erik Van Ooijen ◽  
Joy N. Smith ◽  
Bronte Tilbrook
Keyword(s):  
Coral Reefs ◽  
Continental Shelf ◽  
Great Barrier Reef ◽  
Ocean Acidification ◽  
Seawater Temperature ◽  
Barrier Reef ◽  
Saturation State ◽  
Seawater Acidification ◽  
Seawater Ph ◽  
Seawater Samples

Abstract Coral reefs are highly sensitive to ocean acidification due to rising atmospheric CO2 concentrations. We present 10 years of data (2009–2019) on the long-term trends and sources of variation in the carbon chemistry from two fixed stations in the Australian Great Barrier Reef. Data from the subtropical mid-shelf GBRWIS comprised 3-h instrument records, and those from the tropical coastal NRSYON were monthly seawater samples. Both stations recorded significant variation in seawater CO2 fugacity (fCO2), attributable to seasonal, daytime, temperature and salinity fluctuations. Superimposed over this variation, fCO2 progressively increased by > 2.0 ± 0.3 µatm year−1 at both stations. Seawater temperature and salinity also increased throughout the decade, whereas seawater pH and the saturation state of aragonite declined. The decadal upward fCO2 trend remained significant in temperature- and salinity-normalised data. Indeed, annual fCO2 minima are now higher than estimated fCO2 maxima in the early 1960s, with mean fCO2 now ~ 28% higher than 60 years ago. Our data indicate that carbonate dissolution from the seafloor is currently unable to buffer the Great Barrier Reef against ocean acidification. This is of great concern for the thousands of coral reefs and other diverse marine ecosystems located in this vast continental shelf system.

scholarly journals Assessment of recent advances in measurement techniques for atmospheric carbon dioxide and methane observations

2016 ◽  
Vol 9 (9) ◽  
pp. 4737-4757 ◽  
Author(s):  
Christoph Zellweger ◽  
Lukas Emmenegger ◽  
Mohd Firdaus ◽  
Juha Hatakka ◽  
Martin Heimann ◽  
...  
Keyword(s):  
Carbon Dioxide ◽  
Atmospheric Carbon Dioxide ◽  
Measurement Techniques ◽  
Spectroscopic Techniques ◽  
Cavity Output ◽  
The World ◽  
Atmospheric Carbon ◽  
Carbon Dioxide Co2 ◽  
Improved Accuracy ◽  
Flame Ionisation

Abstract. Until recently, atmospheric carbon dioxide (CO2) and methane (CH4) measurements were made almost exclusively using nondispersive infrared (NDIR) absorption and gas chromatography with flame ionisation detection (GC/FID) techniques, respectively. Recently, commercially available instruments based on spectroscopic techniques such as cavity ring-down spectroscopy (CRDS), off-axis integrated cavity output spectroscopy (OA-ICOS) and Fourier transform infrared (FTIR) spectroscopy have become more widely available and affordable. This resulted in a widespread use of these techniques at many measurement stations. This paper is focused on the comparison between a CRDS "travelling instrument" that has been used during performance audits within the Global Atmosphere Watch (GAW) programme of the World Meteorological Organization (WMO) with instruments incorporating other, more traditional techniques for measuring CO2 and CH4 (NDIR and GC/FID). We demonstrate that CRDS instruments and likely other spectroscopic techniques are suitable for WMO/GAW stations and allow a smooth continuation of historic CO2 and CH4 time series. Moreover, the analysis of the audit results indicates that the spectroscopic techniques have a number of advantages over the traditional methods which will lead to the improved accuracy of atmospheric CO2 and CH4 measurements.

scholarly journals Preservation of terrestrial organic carbon in marine sediments off shore Taiwan: mountain building and atmospheric carbon dioxide sequestration

2013 ◽  
Vol 1 (1) ◽  
pp. 177-206
Author(s):  
S.-J. Kao ◽  
R. G. Hilton ◽  
K. Selvaraj ◽  
M. Dai ◽  
F. Zehetner ◽  
...  
Keyword(s):  
Carbon Dioxide ◽  
Organic Carbon ◽  
Marine Sediments ◽  
Atmospheric Carbon Dioxide ◽  
Climatic Variability ◽  
Deep Ocean ◽  
Sediment Traps ◽  
Terrestrial Biosphere ◽  
Atmospheric Carbon ◽  
Carbon Dioxide Co2

Abstract. Geological sequestration of atmospheric carbon dioxide (CO2) can be achieved by the erosion of organic carbon (OC) from the terrestrial biosphere and its burial in long-lived marine sediments. Rivers on mountain islands of Oceania in the western Pacific have very high rates of OC export to the ocean, yet its preservation offshore remains poorly constrained. Here we use the OC content (Corg, %), radiocarbon (Δ14Corg) and stable isotope (δ13Corg) composition of sediments offshore Taiwan to assess the fate of terrestrial OC. We account for rock-derived fossil OC to assess the preservation of OC eroded from the terrestrial biosphere (non-fossil OC) during flood discharges (hyperpycnal river plumes) and when river inputs are dispersed more widely (hypopycnal). The Corg, Δ14Corg and δ13Corg of marine sediment traps and cores indicate that during flood discharges, terrestrial OC is transferred efficiently to the deep ocean and accumulates offshore with little evidence for terrestrial OC loss. In marine sediments fed by dispersive river inputs, the Corg, Δ14Corg and δ13Corg are consistent with mixing of marine OC and terrestrial OC and suggest that efficient preservation of terrestrial OC (> 70%) is also associated with hypopycnal delivery. Re-burial of fossil OC is pervasive. Our findings from Taiwan suggest that erosion and marine burial of terrestrial non-fossil OC may sequester > 8 TgC yr−1 across Oceania, a significant geological CO2 sink which requires better constraint. We postulate that mountain islands of Oceania provide strong link between tectonic uplift and the carbon cycle, one moderated by the climatic variability that controls terrestrial OC delivery to the ocean.

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