Spatio-Temporal Distribution of Particulate Organic Carbon (POC) and Nitrogen (PON) in the Southwestern Area of East Sea

Author(s):  
Seok Jin Oh ◽  
Semi Jeong ◽  
Seok-Yun Kim
Water ◽  
2019 ◽  
Vol 11 (4) ◽  
pp. 748 ◽  
Author(s):  
Peter Chifflard ◽  
Christina Fasching ◽  
Martin Reiss ◽  
Lukas Ditzel ◽  
Kyle S. Boodoo

Here for the first time, we analyze the concentration of dissolved (DOC) and particulate organic carbon (POC), as well as its optical properties (absorbance and fluorescence) from several proglacial streams across Iceland, the location of Europe’s largest non-polar ice cap. We found high spatial variability of DOC concentrations and dissolved organic matter (DOM) composition during peak melt, sampling 13 proglacial streams draining the 5 main Icelandic glaciers. Although glacial-derived organic matter (OM) was dominated by proteinaceous florescence, organic matter composition was variable among glaciers, often exhibiting relatively higher aromatic content and increased humification (based on absorbance and fluorescence measurements) closer to the glacier terminus, modulated by the presence of glacial lakes. Additional sampling locations the in flow path of the river Hvitá revealed that while POC concentrations decreased downstream, DOC concentrations and the autochthonous fraction of OM increased, suggesting the reworking of the organic carbon by microbial communities, with likely implications for downstream ecosystems as glaciers continue to melt. Based on our measured DOC concentrations ranging from 0.11 mg·L−1 to 0.94 mg·L−1, we estimate a potential annual carbon release of 0.008 ± 0.002 Tg·C·yr−1 from Icelandic glaciers. This non-conservative first estimate serves to highlight the potentially significant contribution of Icelandic pro-glacial streams to the global carbon cycle and the need for the quantification and determination of the spatio-temporal variation of DOC and POC fluxes and their respective drivers, particularly in light of increased rates of melting due to recent trends in climatic warming.


2011 ◽  
Vol 27 (2) ◽  
pp. 107-120 ◽  
Author(s):  
Gi-Hoon Hong ◽  
Yu-Hwan Ahn ◽  
Young-Baek Son ◽  
Joo-Hyung Ryu ◽  
Chang-Joon Kim ◽  
...  

2021 ◽  
Author(s):  
Maria-Theresia Verwega ◽  
Christopher J. Somes ◽  
Markus Schartau ◽  
Robyn E. Tuerena ◽  
Anne Lorrain ◽  
...  

Abstract. Marine particulate organic carbon-13 stable isotope ratios (δ13CPOC) provide insights in understanding carbon cycling through the atmosphere, ocean, and biosphere. They have been used to trace the input of anthropogenic carbon in the marine ecosystem due to the distinct isotopically light signature of anthropogenic emissions. However, δ13CPOC is also significantly altered during photosynthesis by phytoplankton, which complicates its interpretation. For such purposes, robust spatio-temporal coverage of δ13CP OC observations is essential. We collected all such available data sets, merged and homogenized them to provide the largest available marine δ13CPOC data set (Verwega et al., 2021). The data set consists of 4732 data points covering all major ocean basins beginning in the 1960s. We describe the compiled raw data, compare different observational methods, and provide key insights in the temporal and spatial distribution that is consistent with previously observed patterns. The main different sample collection methods (bottle, intake, net, trap) are generally consistent with each other when comparing within regions. An analysis of 1990s mean δ13CP OC values in an meridional section accross the Atlantic Ocean shows relatively high values (≥ −22 ‰) in the low latitudes (< 30°) trending towards lower values in the Arctic Ocean (∼ −24 ‰) and Southern Ocean (≤ −28 ‰). The temporal trend since the 1960s shows a decrease of mean δ13CPOC by more than 3 ‰ in all basins except for the Southern Ocean which shows a weaker trend but contains relatively poor multi-decadal coverage.


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