Characterization and quantification of dissolved organic carbon releases from suspended and sedimented leaf fragments and of residual particulate organic matter

2016 ◽  
Vol 571 ◽  
pp. 269-274 ◽  
Author(s):  
Uranchimeg Bayarsaikhan ◽  
Aki Sebastian Ruhl ◽  
Martin Jekel
2015 ◽  
Vol 12 (13) ◽  
pp. 10545-10578 ◽  
Author(s):  
A. L. Zuijdgeest ◽  
R. Zurbrügg ◽  
N. Blank ◽  
R. Fulcri ◽  
D. B. Senn ◽  
...  

Abstract. Floodplains are important biogeochemical reactors during fluvial transport of carbon and nutrient species towards the oceans. In the tropics and subtropics pronounced rainfall seasonality results in highly dynamic floodplain biogeochemistry. Massive construction of hydropower dams, however, has significantly altered the hydrography and chemical characteristics of many (sub)tropical rivers. In this study, we compare organic matter and nutrient biogeochemistry of two large, contrasting floodplains in the Zambezi River Basin in Southern Africa, the Barotse Plains and the Kafue Flats. Both systems are of comparable size, but differ in anthropogenic influence: while the Barotse Plains are still relatively pristine, the Kafue Flats are bordered by two hydropower dams. While the Barotse Plains retain particles during the wet season, annual yields of particulate organic carbon and nitrogen are higher than previously reported for the Zambezi and other tropical rivers. Enhanced wet-season runoff adds soil-derived dissolved organic carbon and nitrogen to the Zambezi River, with a corresponding increase in the Barotse Plains. Soil-derived organic matter dominates the particulate phase year-round in the Barotse Plains, and a varying influence of C3- and C4-plant vegetation can be observed throughout the year. In contrast to the Barotse Plains, net export of particulate matter from the Kafue Flats has been observed during the wet season, but over an annual cycle, the Kafue Flats are effectively accumulating dissolved carbon and nutrients. In the Kafue Flats, the runoff-induced increase in dissolved organic carbon and nitrogen concentrations is delayed by the upstream dam operation. The dam reservoir also causes a shift in the source of the particulate organic matter – from soil-derived during the dry season to aquatically produced in the wet season – in the downstream Kafue Flats. Spatial zonation in vegetation and temporal flooding dynamics in the Kafue Flats result in mostly C3-derived particulate organic matter during wet season, and a dominance of C4-derived material during dry season. This pattern results from dam-induced changes in vegetation, as dam construction along the Kafue River has led to encroachment of woody plant species onto the Kafue Flats. The two systems exhibit different flooding dynamics, with a~larger contribution of floodplain-derived water in the Kafue Flats and a stronger peak flow in the Barotse Plains. Differences in the biogeochemistry of the two systems that can be linked to the dams are the timing of the runoff-driven dissolved organic carbon and nitrogen pulses in the wet season and the origin and inputs of particulate organic matter. This study reveals clear effects of dam construction on organic matter and nutrient dynamics on the downstream floodplain. Man-made reservoirs alter the origin of organic matter, and change the timing of precipitation-driven carbon and nitrogen pulses. Environmental assessments of dam impacts should therefore consider changes in water quality.


Wetlands ◽  
2020 ◽  
Vol 40 (5) ◽  
pp. 1047-1059
Author(s):  
Daniel A. Saavedra-Hortua ◽  
Daniel A. Friess ◽  
Martin Zimmer ◽  
Lucy Gwen Gillis

Abstract Mangrove forests are among the world’s most productive ecosystems and provide essential ecosystem services such as global climate regulation through the sequestration of carbon. A detailed understanding of the influence of drivers of ecosystem connectivity (in terms of exchange of suspended particulate organic matter), such as geomorphic setting and carbon stocks, among coastal ecosystems is important for being able to depict carbon dynamics. Here, we compared carbon stocks, CO2 fluxes at the sediment-air interface, concentrations of dissolved organic carbon and suspended particulate organic carbon across a mangrove-seagrass-tidal flat seascape. Using stable isotope signatures of carbon and nitrogen in combination with MixSIAR models, we evaluated the contribution of organic matter from different sources among the different seascape components. Generally, carbon concentration was higher as dissolved organic carbon than as suspended particulate matter. Geomorphic settings of the different locations reflected the contributions to particulate organic matter of the primary producers. For example, the biggest contributors in the riverine location were mangrove trees and terrestrial plants, while in fringing locations oceanic and macroalgal sources dominated. Anthropogenic induced changes at the coastal level (i.e. reduction of mangrove forests area) may affect carbon accumulation dynamics in adjacent coastal ecosystems.


2020 ◽  
Vol 55 (2) ◽  
pp. 184-197
Author(s):  
Saeideh Mirzaei ◽  
Beata Gorczyca

Abstract In this study, diffused aeration was applied to remove trihalomethane (THM) compounds from chlorinated, treated water containing high dissolved organic carbon (DOC) of 6.8 ± 1.2 mg/L. Increasing air-to-water volumetric ratio (rA/W) from 16 to 39 enhanced total THM (TTHM) removal from 60 to 70% at 20 °C and from 30 to 50% at 4 °C. Although bromodichloromethane has lower Henry's law constant than chloroform (CF), it was removed by a higher degree than CF in some aeration trials. Albeit obtaining high removals in aeration, TTHM reformed, and their concentration surpassed the Canadian guideline of 100 ppb in about 24 hours at 20 °C and 40 hours at 10 °C in all attempted air-to-water ratios. The water age in the system investigated in this study varied from 48 hours in midpoint chlorine boosting stations to 336 hours in the nearest endpoint. This study showed that THM removal by aeration is not a viable solution to control the concentration of these disinfection by-products in high-DOC treated water and in distribution systems where water age exceeds 24 hours; unless, it is going to be installed at the distribution endpoints.


2008 ◽  
Vol 5 (2) ◽  
pp. 281-298 ◽  
Author(s):  
P. Raimbault ◽  
N. Garcia ◽  
F. Cerutti

Abstract. During the BIOSOPE cruise the RV Atalante was dedicated to study the biogeochemical properties in the South Pacific between the Marquesas Islands (141° W–8° S) and the Chilean upwelling (73° W–34° S). Over the 8000 km covered by the cruise, several different trophic situations were encountered, in particular strong oligotrophic conditions in the South Pacific Gyre (SPG, between 123° W and 101° W). In this isolated region, nitrate was undetectable between the surface and 160–180 m and only trace quantities (<20 nmoles l−1) of regenerated nitrogen (nitrite and ammonium) were detected, even in the subsurface maximum. Integrated nitrate over the photic layer, which reached 165 m, was close to zero. Despite this severe nitrogen-depletion, phosphate was always present in significant concentrations (≈0.1 μmoles l−1), while silicic acid was maintained at low but classical oceanic levels (≈1 μmoles l−1). In contrast, the Marquesas region (MAR) to the west and Chilean upwelling (UPW) to the east were characterized by high nutrient concentrations, one hundred to one thousand fold higher than in the SPG. The distribution of surface chlorophyll reflected the nitrate gradient, the lowest concentrations (0.023 nmoles l−1) being measured at the centre of the SPG, where integrated value throughout the photic layer was very low (≈ 10 mg m−2). However, due to the relatively high concentrations of chlorophyll-a encountered in the DCM (0.2 μg l−1), chlorophyll-a concentrations throughout the photic layer were less variable than nitrate concentrations (by a factor 2 to 5). In contrast to chlorophyll-a, integrated particulate organic matter (POM) remained more or less constant along the study area (500 mmoles m−2, 60 mmoles m−2 and 3.5 mmoles m−2 for particulate organic carbon, particulate organic nitrogen and particulate organic phosphorus, respectively), with the exception of the upwelling, where values were two fold higher. The residence time of particulate carbon in the surface water was only 4–5 days in the upwelling, but up to 30 days in the SPG, where light isotopic δ15N signal noted in the suspended POM suggests that N2-fixation provides a dominant supply of nitrogen to phytoplankton. The most striking feature was the large accumulation of dissolved organic matter (DOM) in the SPG compared to the surrounding waters, in particular dissolved organic carbon (DOC) where concentrations were at levels rarely measured in oceanic waters (>100 μmoles l−1). Due to this large pool of DOM in the SPG photic layer, integrated values followed a converse geographical pattern to that of inorganic nutrients with a large accumulation in the centre of the SPG. Whereas suspended particulate matter in the mixed layer had a C/N ratio largely conforming to the Redfield stochiometry (C/N≈6.6), marked deviations were observed in this excess DOM (C/N≈16 to 23). The marked geographical trend suggests that a net in situ source exists, mainly due to biological processes. Thus, in spite of strong nitrate-depletion leading to low chlorophyll biomass, the closed ecosystem of the SPG can accumulate large amounts of C-rich dissolved organic matter. The implications of this finding are examined, the conclusion being that, due to weak lateral advection, the biologically produced dissolved organic carbon can be accumulated and stored in the photic layer for very long periods. In spite of the lack of seasonal vertical mixing, a significant part of new production (up to 34%), which was mainly supported by dinitrogen fixation, can be exported to deep waters by turbulent diffusion in terms of DOC. The diffusive rate estimated in the SPG (134 μmolesC m−2 d−1), was quite equivalent to the particles flux measured by sediments traps.


2008 ◽  
Vol 65 (3) ◽  
pp. 543-548 ◽  
Author(s):  
Yves T Prairie

In this perspective article, I argue that dissolved organic carbon occupies a central role in the functioning of lake ecosystems, comparable in importance to that played by nutrients. Because lakes receive so much dissolved organic carbon from the terrestrial landscape, its accumulation in water bodies usually represents the largest pool of lacustrine organic matter within the water column. The transformation of even a small fraction of this external carbon by the microbial community can alter significantly the metabolic balance of lake ecosystems, simultaneously releasing carbon dioxide to the atmosphere and burying organic carbon in lake sediments. At the landscape level, even if they occupy a small fraction of the landscape, lakes play a surprisingly important role in the regional carbon budget, particularly when considered at the appropriate temporal scale.


2004 ◽  
Vol 4 (4) ◽  
pp. 113-119 ◽  
Author(s):  
C.A. Murray ◽  
S.A. Parsons

Advanced oxidation processes have been reported to have the potential to remove natural organic matter from source waters. Of these Fenton's reagent, photo-Fenton's reagent and titanium dioxide photocatalysis are the three most promising processes. Compared to conventional coagulation/flocculation processes they have higher removal efficiencies in terms of both dissolved organic carbon and UV254 absorbance. Under optimum reaction conditions all three remove over 80% dissolved organic carbon and 0% UV254 absorbance. In addition the enhanced removal of natural organic matter leads to a corresponding reduction in the formation of disinfection by-products following chlorination of the treated water. Advanced oxidation processes give enhanced removal of organic species ranging from low to high molecular weight while coagulation/flocculation is inefficient at removing low molecular weight species. One additional benefit is all three processes produce less residuals compared to conventional coagulation, which is advantageous as the disposal of such residuals normally contributes a large proportion of the costs at water treatment works.


2015 ◽  
Vol 12 (18) ◽  
pp. 15655-15685
Author(s):  
Z.-Y. Zhu ◽  
Y. Wu ◽  
S.-M. Liu ◽  
F. Wenger ◽  
J. Hu ◽  
...  

Abstract. In the face of ongoing global warming and glacier retreat, the composition and flux of organic matter in glacier–fjord systems are key variables for updating the carbon cycle and budget, whereas the role of Arctic valley glaciers seems unimportant when compared with the huge Greenland Ice Sheet. Our field observations of the glacier-fed Bayelva River, Svalbard, and the adjacent Kongsfjorden allowed us to determine the compositions of particulate organic matter from glacier to fjord and also to estimate the flux of organic carbon, both for the river and for Svalbard in general. Particulate organic carbon (POC) and dissolved organic carbon (DOC) in the Bayelva River averaged 56 and 73 μM, respectively, in August 2012. Amino acids (AAs) and phytoplankton pigments accounted for ~ 10 % of the particulate organic matter (POM) in the Bayelva River, while AAs represented > 90 % of particulate nitrogen in fjord surface water, suggesting the strong in situ assimilation of organic matter. Bacteria accounts for 13 and 19 % of the POC in the Bayelva River and the Kongsfjorden, respectively, while values for particulate nitrogen (PN) are much higher (i.e., 36 % in Kongsfjorden). The total discharge from the Bayelva River in 2012 was 29 × 106 m3. Furthermore, we calculated the annual POC, DOC, and PN fluxes for the river as 20 ± 1.6, 25 ± 5.6, and 4.7 ± 0.75 t, respectively. Using the POC content and DOC concentration data, we then estimated the annual POC and DOC fluxes for Svalbard glaciers. Although the estimated POC (0.056 ± 0.02 × 106 t yr−1) and DOC (0.02 ± 0.01 × 106 t yr−1) fluxes of Svalbard glaciers are small compared with those of the Greenland Ice Sheet, the area-weighted POC flux of Svalbard glaciers is twice that of the Greenland Ice Sheet, while the flux of DOC can be 4 to 7 times higher. Therefore, we propose that valley glaciers are efficient high-latitude sources of organic carbon.


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