scholarly journals Summer rainfall dissolved organic carbon, solute, and sediment fluxes in a small Arctic coastal catchment on Herschel Island (Yukon Territory, Canada)

2018 ◽  
Vol 4 (4) ◽  
pp. 750-780 ◽  
Author(s):  
Caroline Coch ◽  
Scott F. Lamoureux ◽  
Christian Knoblauch ◽  
Isabell Eischeid ◽  
Michael Fritz ◽  
...  

Coastal ecosystems in the Arctic are affected by climate change. As summer rainfall frequency and intensity are projected to increase in the future, more organic matter, nutrients and sediment could be mobilized and transported into the coastal nearshore zones. However, knowledge of current processes and future changes is limited. We investigated streamflow dynamics and the impacts of summer rainfall on lateral fluxes in a small coastal catchment on Herschel Island in the western Canadian Arctic. For the summer monitoring periods of 2014–2016, mean dissolved organic matter flux over 17 days amounted to 82.7 ± 30.7 kg km−2 and mean total dissolved solids flux to 5252 ± 1224 kg km−2. Flux of suspended sediment was 7245 kg km−2 in 2015, and 369 kg km−2 in 2016. We found that 2.0% of suspended sediment was composed of particulate organic carbon. Data and hysteresis analysis suggest a limited supply of sediments; their interannual variability is most likely caused by short-lived localized disturbances. In contrast, our results imply that dissolved organic carbon is widely available throughout the catchment and exhibits positive linear relationship with runoff. We hypothesize that increased projected rainfall in the future will result in a similar increase of dissolved organic carbon fluxes.

2021 ◽  
Author(s):  
Rene Preusker ◽  
Jan El Kassar ◽  
Bennet Juhls

<p>As air temperatures in the Arctic continue to rise, permafrost thaw intensifies, and discharge from the Arctic rivers increases. These drastic changes are likely to accelerate mobilization of organic matter and its export through rivers into the Arctic Ocean. Therefore, thorough monitoring of these processes becomes increasingly important. The Lena River with its large catchment area is one of the major sources of the organic carbon in the Arctic Ocean and, therefore, plays a crucial role in the Arctic carbon cycle. <br>To observe current and future changes of carbon transport via the Lena River, a new monitoring program has been initiated in 2018. In situ water samples are collected from the one of the Lena Delta branches every several days. Since generally the in situ sampling in the Arctic is challenging and costly, in this study, we test the potential of remote sensing to complement the field observations. Remote sensing provides synoptic spatial coverages and high temporal resolution at high latitudes. <br>We test the retrieval of dissolved organic carbon (DOC) from satellite-derived chromophoric dissolved organic matter (CDOM). For this, we use measurements of the Ocean & Land Colour Instrument (OLCI) on board the Sentinel-3 satellites in combination with beforehand tested atmospheric correction algorithms and CDOM retrieval algorithms. The quality of the satellite retrieved DOC of the Lena River water is assessed by DOC, measured in the in situ samples. Remotely sensed DOC contributes to an improvement of DOC fluxes monitoring, which can potentially be extended to all big Arctic rivers.</p>


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.


2014 ◽  
Vol 6 (1) ◽  
pp. 619-655
Author(s):  
S. Zubrzycki ◽  
L. Kutzbach ◽  
E.-M. Pfeiffer

Abstract. Permafrost-affected soils have accumulated enormous pools of organic matter during the Quaternary Period. The area occupied by these soils amounts to more than 8.6 million km2, which is about 27% of all land areas north of 50° N. Therefore, permafrost-affected soils are considered to be one of the most important cryosphere elements within the climate system. Due to the cryopedogenic processes that form these particular soils and the overlying vegetation that is adapted to the arctic climate, organic matter has accumulated to the present extent of up to 1024 Pg (1 Pg = 1015 g = 1 Gt) of soil organic carbon stored within the uppermost three meters of ground. Considering the observed progressive climate change and the projected polar amplification, permafrost-affected soils will undergo fundamental property changes. Higher turnover and mineralization rates of the organic matter are consequences of these changes, which are expected to result in an increased release of climate-relevant trace gases into the atmosphere. As a result, permafrost regions with their distinctive soils are likely to trigger an important tipping point within the global climate system, with additional political and social implications. The controversy of whether permafrost regions continue accumulating carbon or already function as a carbon source remains open until today. An increased focus on this subject matter, especially in underrepresented Siberian regions, could contribute to a more robust estimation of the soil organic carbon pool of permafrost regions and at the same time improve the understanding of the carbon sink and source functions of permafrost-affected soils.


2015 ◽  
Vol 12 (23) ◽  
pp. 6915-6930 ◽  
Author(s):  
J. E. Vonk ◽  
S. E. Tank ◽  
P. J. Mann ◽  
R. G. M. Spencer ◽  
C. C. Treat ◽  
...  

Abstract. As Arctic regions warm and frozen soils thaw, the large organic carbon pool stored in permafrost becomes increasingly vulnerable to decomposition or transport. The transfer of newly mobilized carbon to the atmosphere and its potential influence upon climate change will largely depend on the degradability of carbon delivered to aquatic ecosystems. Dissolved organic carbon (DOC) is a key regulator of aquatic metabolism, yet knowledge of the mechanistic controls on DOC biodegradability is currently poor due to a scarcity of long-term data sets, limited spatial coverage of available data, and methodological diversity. Here, we performed parallel biodegradable DOC (BDOC) experiments at six Arctic sites (16 experiments) using a standardized incubation protocol to examine the effect of methodological differences commonly used in the literature. We also synthesized results from 14 aquatic and soil leachate BDOC studies from across the circum-arctic permafrost region to examine pan-arctic trends in BDOC. An increasing extent of permafrost across the landscape resulted in higher DOC losses in both soil and aquatic systems. We hypothesize that the unique composition of (yedoma) permafrost-derived DOC combined with limited prior microbial processing due to low soil temperature and relatively short flow path lengths and transport times, contributed to a higher overall terrestrial and freshwater DOC loss. Additionally, we found that the fraction of BDOC decreased moving down the fluvial network in continuous permafrost regions, i.e. from streams to large rivers, suggesting that highly biodegradable DOC is lost in headwater streams. We also observed a seasonal (January–December) decrease in BDOC in large streams and rivers, but saw no apparent change in smaller streams or soil leachates. We attribute this seasonal change to a combination of factors including shifts in carbon source, changing DOC residence time related to increasing thaw-depth, increasing water temperatures later in the summer, as well as decreasing hydrologic connectivity between soils and surface water as the thaw season progresses. Our results suggest that future climate warming-induced shifts of continuous permafrost into discontinuous permafrost regions could affect the degradation potential of thaw-released DOC, the amount of BDOC, as well as its variability throughout the Arctic summer. We lastly recommend a standardized BDOC protocol to facilitate the comparison of future work and improve our knowledge of processing and transport of DOC in a changing Arctic.


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