scholarly journals Humic surface waters of frozen peat bogs (permafrost zone) are highly resistant to bio- and photodegradation

Author(s):  
Liudmila S. Shirokova ◽  
Artem V. Chupakov ◽  
Svetlana A. Zabelina ◽  
Natalia V. Neverova ◽  
Dahedrey Payandi-Rolland ◽  
...  

Abstract. Bio- and photo-degradation of dissolved organic matter (DOM) is identified as dominant vector of C cycle in boreal and high-latitude surface waters. In contrast to large number of studies of humic waters from permafrost-free regions and oligotrophic waters from permafrost-bearing regions, the bio- and photo-lability of DOM from humic surface waters of permafrost-bearing regions has not been thoroughly evaluated. Following standardized methods, we measured biodegradation (low, intermediate, high temperature) and photodegradation (one intermediate temperature) of DOM in surface waters along the hydrological continuum (depression → stream → thermokarst lake → river Pechora) within a European Russian frozen peatland. In all systems, there was no measurable (≥ 10 %) bio- or photodegradation of DOM over 1 month of incubation. It is possible that the main cause of the lack of degradation is the dominance of allochthonous refractory (soil, peat) DOM in all studied waters. Yet, all surface waters were supersaturated with CO2. Thus, this study suggest that, rather than bio- and photo-degradation of DOM in the water column, other factors such as peat porewater DOM processing and respiration of sediments are the main drivers of elevated pCO2 and emission in humic boreal waters of frozen peat bogs.

2019 ◽  
Vol 16 (12) ◽  
pp. 2511-2526 ◽  
Author(s):  
Liudmila S. Shirokova ◽  
Artem V. Chupakov ◽  
Svetlana A. Zabelina ◽  
Natalia V. Neverova ◽  
Dahedrey Payandi-Rolland ◽  
...  

Abstract. In contrast to the large number of studies on humic waters from permafrost-free regions and oligotrophic waters from permafrost-bearing regions, the bio- and photolability of DOM from the humic surface waters of permafrost-bearing regions has not been thoroughly evaluated. Following standardized protocol, we measured biodegradation (at low, intermediate and high temperatures) and photodegradation (at one intermediate temperature) of DOM in surface waters along the hydrological continuum (depression → stream → thermokarst lake → Pechora River) within a frozen peatland in European Russia. In all systems, within the experimental resolution of 5 % to 10 %, there was no bio- or photodegradation of DOM over a 1-month incubation period. It is possible that the main cause of the lack of degradation is the dominance of allochthonous refractory (soil, peat) DOM in all waters studied. However, all surface waters were supersaturated with CO2. Thus, this study suggests that, rather than bio- and photodegradation of DOM in the water column, other factors such as peat pore-water DOM processing and respiration of sediments are the main drivers of elevated pCO2 and CO2 emission in humic boreal waters of frozen peat bogs.


2013 ◽  
Vol 10 (11) ◽  
pp. 6945-6956 ◽  
Author(s):  
M. Gonsior ◽  
P. Schmitt-Kopplin ◽  
D. Bastviken

Abstract. Transformations of dissolved organic matter (DOM) in boreal lakes lead to large greenhouse gas emissions as well as substantial carbon storage in sediments. Using novel molecular characterization approaches and photochemical degradation experiments we studied how seasonal patterns in water column stratification affected the DOM in a Swedish lake under early spring and summer conditions. Dissolved organic carbon (DOC) concentrations were consistently higher above the sediment when compared to surface waters throughout the sampling periods. Photobleaching alone could not explain this difference in DOC because the lake was covered by 40 cm-thick ice during late winter sampling and still showed the same DOC trend. The differences in the molecular diversity between surface DOM in winter and summer were consistent with ongoing photobleaching/decarboxylation and a possible bacterial consumption of photo-products. Additional photo-degradation experiments using simulated sunlight showed a production of highly oxidized organic molecules and low molecular weight compounds in all late winter samples and also in the deep water sample in summer. In the surface summer DOM sample, few such molecules were produced during the photo-degradation experiments, confirming that DOM was already photobleached prior to the experiments. This study suggests that photobleaching, and therefore also the ice cover during winter, plays a central role in surface DOM transformation, with important differences in the molecular composition of DOM between surface and deep boreal lake waters. The release of DOC from boreal lake sediments also contribute to this pattern. Photochemical degradation of DOM may be more extensive following ice-out and water column turnover when non-light exposed and thereby photosensitive DOM is photo-mineralized. Hence, the yearly DOM photo-mineralization may be greater than inferred from studies of recently light-exposed DOM.


2014 ◽  
Vol 11 (10) ◽  
pp. 14097-14132 ◽  
Author(s):  
L. Tremblay ◽  
J. Caparros ◽  
K. Leblanc ◽  
I. Obernosterer

Abstract. Natural iron fertilization of high-nutrient low-chlorophyll (HNLC) waters induces annually occurring spring phytoplankton blooms off Kerguelen Islands (Southern Ocean). To examine the origin and fate of particulate and dissolved organic matter (POM and DOM), D- and L-amino acids (AA) were quantified at bloom and HNLC stations. Total hydrolysable AA accounted for 21–25% of surface particulate organic carbon (%POCAA) at the bloom sites, but for 10% at the HNLC site. A marked decrease in %POCAA with depth was observed at the most productive stations leading to values between 3 and 5% below 300 m depth. AA contributed to only 0.9–4.4% of dissolved organic carbon (%DOCAA) at all stations. The only consistent vertical trend was observed at the most productive station (A3-2) where %DOCAA decreased from ∼2% in the surface waters to 0.9% near 300 m. These AA yields and other markers revealed that POM and DOM were more rapidly altered or mineralized at the bloom sites compared to the HNLC site. Different molecular markers indicated that POM mostly originated from diatoms and bacteria. The estimated average proportion of POM from intact phytoplankton cells in surface waters was 45% at the bloom station A3-2, but 14% at the HNLC site. Estimates based on D-AA yields indicated that ∼15% of POM and ∼30% of DOM was of bacterial origin (cells and cell fragments) at all stations. Surprisingly, the DOM in HNLC waters appeared less altered than the DOM from the bloom, had slightly higher dissolved AA concentrations, and showed no sign of alteration within the water column. Unfavorable conditions for bacterial degradation in HNLC regions can explain these findings. In contrast, large inputs of labile organic molecules and iron, likely stimulate the degradation of organic matter (priming effect) and the production of more recalcitrant DOM (microbial carbon pump) during iron-fertilized blooms.


2015 ◽  
Vol 56 (69) ◽  
pp. 1-8 ◽  
Author(s):  
Mats A. Granskog ◽  
Daiki Nomura ◽  
Susann Müller ◽  
Andreas Krell ◽  
Takenobu Toyota ◽  
...  

AbstractAbsorption and fluorescence of chromophoric dissolved organic matter (CDOM) in sea ice and surface waters in the southern Sea of Okhotsk was examined. Sea-water CDOM had featureless absorption increasing exponentially with shorter wavelengths. Sea ice showed distinct absorption peaks in the ultraviolet, especially in younger ice. Older first-year sea ice had relatively flat absorption spectra in the ultraviolet range. Parallel factor analysis (PARAFAC) identified five fluorescent CDOM components, two humic-like and three protein-like. Sea water was largely governed by humic-like fluorescence. In sea ice, protein-like fluorescence was found in considerable excess relative to sea water. The accumulation of protein-like CDOM fluorescence in sea ice is likely a result of biological activity within the ice. Nevertheless, sea ice does not contribute excess CDOM during melt, but the material released will be of different composition than that present in the underlying waters. Thus, at least transiently, the CDOM introduced during sea-ice melt might provide a more labile source of fresher protein-like DOM to surface waters in the southern Sea of Okhotsk.


Soil Research ◽  
2019 ◽  
Vol 57 (3) ◽  
pp. 294 ◽  
Author(s):  
Xiaojie Wang ◽  
Guanhong Chen ◽  
Renduo Zhang

The temperature sensitivity of multiple carbon (C) pools in the soil plays an important role in the C cycle and potential feedback to climate change. The aim of this study was to investigate the temperature sensitivity of different biochars in soil to better understand the temperature sensitivity of different soil C pools. Biochars were prepared using sugarcane residue at temperatures of 300, 500 and 800°C (representing different C pools) and C skeletons (representing the refractory C pool in biochar) were obtained from each biochar. The sugarcane residue, biochars and C skeletons were used as amendments in a simulated soil with microbes but without organic matter. The temperature sensitivity of the amended soils was characterised by their mineralisation rate changes in response to ambient temperatures. The temperature sensitivity of treatments with relatively refractory biochars was higher than that with labile biochars. The temperature sensitivity of treatments with biochars was lower than for their corresponding C skeletons. The different temperature sensitivity of treatments was attributable to the different internal C structures (i.e. the functional groups of C=C and aromatic structure) of amendments, determining the biodegradability of substrates. Dissolved organic matter and microbial enzyme activity of biochars were lower than those of corresponding C skeletons, and decreased with increasing pyrolysis temperature. The temperature sensitivities of treatments with biochars, C skeletons and sugarcane residue were negatively correlated with the properties of dissolved organic matter and microbial enzyme activities (especially dehydrogenase) in soil.


2020 ◽  
Vol 6 (9) ◽  
pp. 2365-2381
Author(s):  
Zachary T. Kralles ◽  
Kaoru Ikuma ◽  
Ning Dai

Peracetic acid pre-oxidation of algal impacted waters can reduce formation of trihalomethanes but promote formation of haloacetonitriles, due to the degradation of dissolved organic matter and coincident release of intracellular organic matter.


2013 ◽  
Vol 10 (11) ◽  
pp. 7207-7217 ◽  
Author(s):  
Y. Yamashita ◽  
Y. Nosaka ◽  
K. Suzuki ◽  
H. Ogawa ◽  
K. Takahashi ◽  
...  

Abstract. Chromophoric dissolved organic matter (CDOM) ubiquitously occurs in marine environments and plays a significant role in the marine biogeochemical cycles. Basin scale distributions of CDOM have recently been surveyed in the global ocean and indicate that quantity and quality of oceanic CDOM are mainly controlled by in situ production and photobleaching. However, factors controlling the spectral parameters of CDOM in the UV region, i.e., spectral slope of CDOM determined at 275–295 nm (S275–295) and the ratio of two spectral slope parameters (SR); the ratio of S275–295 to S350–400, have not been well documented. To evaluate the factor controlling the spectral characteristics of CDOM in the UV region in the open ocean, we determined the quantitative and qualitative characteristics of CDOM in the subarctic and subtropical surface waters (5–300 m) of the western North Pacific. Absorption coefficients at 320 nm in the subarctic region were higher than those in the subtropical region throughout surface waters, suggesting that magnitudes of photobleaching were different between the two regions. The values of S275–295 and SR were also higher in the subtropical region than the subarctic region. The dark microbial incubation showed biodegradation of DOM little affected S275–295, but slightly decreased SR. On the other hand, increases in S275–295 and relative stableness of SR were observed during photo-irradiation incubations respectively. These experimental results indicated that photobleaching of CDOM mainly induced qualitative differences in CDOM at UV region between the subarctic and subtropical surface waters. The results of this study imply that S275–295 can be used as a tracer of photochemical history of CDOM in the open ocean.


Geoderma ◽  
2003 ◽  
Vol 113 (3-4) ◽  
pp. 397-411 ◽  
Author(s):  
Stephan Glatzel ◽  
Karsten Kalbitz ◽  
Mike Dalva ◽  
Tim Moore

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