scholarly journals Major Effects of Alkalinity on the Relationship Between Metabolism and Dissolved Inorganic Carbon Dynamics in Lakes

Ecosystems ◽  
2020 ◽  
Vol 23 (8) ◽  
pp. 1566-1580 ◽  
Author(s):  
Hares Khan ◽  
Alo Laas ◽  
Rafael Marcé ◽  
Biel Obrador

AbstractSeveral findings suggest that CO2 emissions in lakes are not always directly linked to changes in metabolism but can be associated with interactions with the dissolved inorganic carbon equilibrium. Alkalinity has been described as a determining factor in regulating the relative contributions of biological and inorganic processes to carbon dynamics in lakes. Here we analyzed the relationship between metabolic changes in dissolved oxygen (DO) and dissolved inorganic carbon (DIC) at different timescales in eight lakes covering a wide range in alkalinity. We used high-frequency data from automatic monitoring stations to explore the sensitivity of DIC to metabolic changes inferred from oxygen. To overcome the problem of noisy data, commonly found in high-frequency measurements datasets, we used Singular Spectrum Analysis to enhance the diel signal-to-noise ratio. Our results suggest that in most of the studied lakes, a large part of the measured variability in DO and DIC reflects non-metabolic processes. Furthermore, at low alkalinity, DIC dynamics appear to be mostly driven by aquatic metabolism, but this relationship weakens with increasing alkalinity. The observed deviations from the metabolic 1:1 stoichiometry between DO and DIC were strongly correlated with the deviations expected to occur from calcite precipitation, with a stronger correlation when accounting also for the benthic contribution of calcite precipitation. This highlights the role of calcite precipitation as an important driver of CO2 supersaturation in lakes with alkalinity above 1 meq L−1, which represents 57% of the global area of lakes and reservoirs around the world.

2012 ◽  
Vol 117 (G2) ◽  
pp. n/a-n/a ◽  
Author(s):  
Cristian Estop-Aragonés ◽  
Klaus-Holger Knorr ◽  
Christian Blodau

Radiocarbon ◽  
2016 ◽  
Vol 58 (3) ◽  
pp. 549-563 ◽  
Author(s):  
C Coularis ◽  
N Tisnérat-Laborde ◽  
L Pastor ◽  
F Siclet ◽  
M Fontugne

AbstractIn order to map the freshwater reservoir effect (FRE) variability of the Loire River and its tributaries, spatial and temporal carbon isotope (13C and 14C) analyses of the dissolved inorganic carbon (DIC) were conducted. Sites were selected to represent the diversity of geological settings, soil type, and land use. Results show a large spatial variability of 14C FRE ranging between 135 and 2251±30 yr, objectively correlated to DIC contents and alkalinity. Deeper investigations of the relationship between 14C activity of DIC and environmental variables show that the geological substrate is the dominant factor in the 14C reservoir effect, and far more influential than the river flow discharge.


2015 ◽  
Vol 12 (22) ◽  
pp. 6761-6779 ◽  
Author(s):  
C. Hauri ◽  
S. C. Doney ◽  
T. Takahashi ◽  
M. Erickson ◽  
G. Jiang ◽  
...  

Abstract. We present 20 years of seawater inorganic carbon measurements collected along the western shelf and slope of the Antarctic Peninsula. Water column observations from summertime cruises and seasonal surface underway pCO2 measurements provide unique insights into the spatial, seasonal, and interannual variability in this dynamic system. Discrete measurements from depths > 2000 m align well with World Ocean Circulation Experiment observations across the time series and underline the consistency of the data set. Surface total alkalinity and dissolved inorganic carbon data showed large spatial gradients, with a concomitant wide range of Ωarag (< 1 up to 3.9). This spatial variability was mainly driven by increasing influence of biological productivity towards the southern end of the sampling grid and meltwater input along the coast towards the northern end. Large inorganic carbon drawdown through biological production in summer caused high near-shore Ωarag despite glacial and sea-ice meltwater input. In support of previous studies, we observed Redfield behavior of regional C / N nutrient utilization, while the C / P (80.5 ± 2.5) and N / P (11.7 ± 0.3) molar ratios were significantly lower than the Redfield elemental stoichiometric values. Seasonal salinity-based predictions of Ωarag suggest that surface waters remained mostly supersaturated with regard to aragonite throughout the study. However, more than 20 % of the predictions for winters and springs between 1999 and 2013 resulted in Ωarag < 1.2. Such low levels of Ωarag may have implications for important organisms such as pteropods. Even though we did not detect any statistically significant long-term trends, the combination of on\\-going ocean acidification and freshwater input may soon induce more unfavorable conditions than the ecosystem experiences today.


2016 ◽  
Vol 10 (5) ◽  
pp. 2173-2189 ◽  
Author(s):  
Nicolas-Xavier Geilfus ◽  
Ryan J. Galley ◽  
Brent G. T. Else ◽  
Karley Campbell ◽  
Tim Papakyriakou ◽  
...  

Abstract. The precipitation of ikaite and its fate within sea ice is still poorly understood. We quantify temporal inorganic carbon dynamics in sea ice from initial formation to its melt in a sea ice–seawater mesocosm pool from 11 to 29 January 2013. Based on measurements of total alkalinity (TA) and total dissolved inorganic carbon (TCO2), the main processes affecting inorganic carbon dynamics within sea ice were ikaite precipitation and CO2 exchange with the atmosphere. In the underlying seawater, the dissolution of ikaite was the main process affecting inorganic carbon dynamics. Sea ice acted as an active layer, releasing CO2 to the atmosphere during the growth phase, taking up CO2 as it melted and exporting both ikaite and TCO2 into the underlying seawater during the whole experiment. Ikaite precipitation of up to 167 µmolkg−1 within sea ice was estimated, while its export and dissolution into the underlying seawater was responsible for a TA increase of 64–66 µmolkg−1 in the water column. The export of TCO2 from sea ice to the water column increased the underlying seawater TCO2 by 43.5 µmolkg−1, suggesting that almost all of the TCO2 that left the sea ice was exported to the underlying seawater. The export of ikaite from the ice to the underlying seawater was associated with brine rejection during sea ice growth, increased vertical connectivity in sea ice due to the upward percolation of seawater and meltwater flushing during sea ice melt. Based on the change in TA in the water column around the onset of sea ice melt, more than half of the total ikaite precipitated in the ice during sea ice growth was still contained in the ice when the sea ice began to melt. Ikaite crystal dissolution in the water column kept the seawater pCO2 undersaturated with respect to the atmosphere in spite of increased salinity, TA and TCO2 associated with sea ice growth. Results indicate that ikaite export from sea ice and its dissolution in the underlying seawater can potentially hamper the effect of oceanic acidification on the aragonite saturation state (Ωaragonite) in fall and in winter in ice-covered areas, at the time when Ωaragonite is smallest.


Radiocarbon ◽  
2001 ◽  
Vol 43 (2B) ◽  
pp. 821-830 ◽  
Author(s):  
Mariana Stiller ◽  
Aaron Kaufman ◽  
Israel Carmi ◽  
Genia Mintz

The source of endogenic organic and inorganic carbon in lacustrine sediments is the dissolved inorganic carbon (DIC) in the lake water. The relation between the radiocarbon levels of DIC in Lake Kinneret and of CO2 in the atmosphere has been investigated. The ratio of the former to the latter was found to be 0.814 ± 0.013. This ratio is used for calibrating the age of the sediment according to the natural fluctuations in the atmospheric levels of 14C that occurred during the past 10,000 years.


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