The role of irrigation runoff and winter rainfall on dissolved organic carbon loads in an agricultural watershed

USGS Publications Warehouse

Oh, Neung-Hwan; Pellerin, Brian A.; Bachand, Philip A.M.; Hernes, Peter J.; Bachand, Sandra M.; Ohara, Noriaki; Kavvas, M. Levent; Bergamaschi, Brian A.; Horwath, William R.

2013-01-01

We investigated the role of land use/land cover and agriculture practices on stream dissolved organic carbon (DOC) dynamics in the Willow Slough watershed (WSW) from 2006 to 2008. The 415 km2watershed in the northern Central Valley, California is covered by 31% of native vegetation and the remaining 69% of agricultural fields (primarily alfalfa, tomatoes, and rice). Stream discharge and weekly DOC concentrations were measured at eight nested subwatersheds to estimate the DOC loads and yields (loads/area) using the USGS developed stream load estimation model, LOADEST. Stream DOC concentrations peaked at 18.9 mg L−1 during summer irrigation in the subwatershed with the highest percentage of agricultural land use, demonstrating the strong influence of agricultural activities on summer DOC dynamics. These high concentrations contributed to DOC yields increasing up to 1.29 g m−2 during the 6 month period of intensive agricultural activity. The high DOC yields from the most agricultural subwatershed during the summer irrigation period was similar throughout the study, suggesting that summer DOC loads from irrigation runoff would not change significantly in the absence of major changes in crops or irrigation practices. In contrast, annual DOC yields varied from 0.89 to 1.68 g m−2 yr−1 for the most agricultural watershed due to differences in winter precipitation. This suggests that variability in the annual DOC yields will be largely determined by the winter precipitation, which can vary significantly from year to year. Changes in precipitation patterns and intensities as well as agricultural practices have potential to considerably alter the DOC dynamics.

Characteristics of dissolved organic matter in the Upper Klamath River, Lost River, and Klamath Straits Drain, Oregon and California

USGS Publications Warehouse

Goldman, Jami H.; Sullivan, Annett B.

2017-12-11

Concentrations of particulate organic carbon (POC) and dissolved organic carbon (DOC), which together comprise total organic carbon, were measured in this reconnaissance study at sampling sites in the Upper Klamath River, Lost River, and Klamath Straits Drain in 2013–16. Optical absorbance and fluorescence properties of dissolved organic matter (DOM), which contains DOC, also were analyzed. Parallel factor analysis was used to decompose the optical fluorescence data into five key components for all samples. Principal component analysis (PCA) was used to investigate differences in DOM source and processing among sites.At all sites in this study, average DOC concentrations were higher than average POC concentrations. The highest DOC concentrations were at sites in the Klamath Straits Drain and at Pump Plant D. Evaluation of optical properties indicated that Klamath Straits Drain DOM had a refractory, terrestrial source, likely extracted from the interaction of this water with wetland peats and irrigated soils. Pump Plant D DOM exhibited more labile characteristics, which could, for instance, indicate contributions from algal or microbial exudates. The samples from Klamath River also had more microbial or algal derived material, as indicated by PCA analysis of the optical properties. Most sites, except Pump Plant D, showed a linear relation between fluorescent dissolved organic matter (fDOM) and DOC concentration, indicating these measurements are highly correlated (R2=0.84), and thus a continuous fDOM probe could be used to estimate DOC loads from these sites.

Comparing Stream DOC Fluxes from Sensor- and Sample-Based Approaches

NASA Astrophysics Data System (ADS)

Shanley, J. B.; Saraceno, J.; Aulenbach, B. T.; Mast, A.; Clow, D. W.; Hood, K.; Walker, J. F.; Murphy, S. F.; Torres-Sanchez, A.; Aiken, G.; McDowell, W. H.

2015-12-01

DOC transport by streamwater is a significant flux that does not consistently show up in ecosystem carbon budgets. In an effort to quantify stream DOC flux, we analyzed three to four years of high-frequency in situ fluorescing dissolved organic matter (FDOM) concentrations and turbidity measured by optical sensors at the five diverse forested and/or alpine headwater sites of the U.S. Geological Survey (USGS) Water, Energy, and Biogeochemical Budgets (WEBB) program. FDOM serves as a proxy for DOC. We also took discrete samples over a range of hydrologic conditions, using both manual weekly and automated event-based sampling. After compensating FDOM for temperature effects and turbidity interference - which was successful even at the high-turbidity Luquillo, PR site -- we evaluated the DOC-FDOM relation based on discrete sample DOC analyses matched to corrected FDOM at the time of sampling. FDOM was a moderately robust predictor of DOC, with r2 from 0.60 to more than 0.95 among sites. We then formed continuous DOC time series by two independent approaches: (1) DOC predicted from FDOM; and (2) the composite method, based on modeled DOC from regression on stream discharge, season, air temperature, and time, forcing the model to observations and adjusting modeled concentrations between observations by linearly-interpolated model residuals. DOC flux from each approach was then computed directly as concentration times discharge. DOC fluxes based on the sensor approach were consistently greater than the sample-based approach. At Loch Vale, CO (2.5 years) and Panola Mountain GA (1 year), the difference was 5-17%. At Sleepers River, VT (3 years), preliminary differences were greater than 20%. The difference is driven by the highest events, but we are investigating these results further. We will also present comparisons from Luquillo, PR, and Allequash Creek, WI. The higher sensor-based DOC fluxes could result from their accuracy during hysteresis, which is difficult to model. In at least one case the higher sensor-based DOC flux was linked to an unsampled event outside the range of the concentration model. Sensors require upkeep and vigilance with the data, but have the potential to yield more accurate fluxes than sample-based approaches.

Reforestation in southern China: revisiting soil N mineralization and nitrification after 8 years restoration

NASA Astrophysics Data System (ADS)

Mo, Qifeng; Li, Zhi'An; Zhu, Weixing; Zou, Bi; Li, Yingwen; Yu, Shiqin; Ding, Yongzhen; Chen, Yao; Li, Xiaobo; Wang, Faming

2016-01-01

Nitrogen availability and tree species selection play important roles in reforestation. However, long-term field studies on the effects and mechanisms of tree species composition on N transformation are very limited. Eight years after tree seedlings were planted in a field experiment, we revisited the site and tested how tree species composition affects the dynamics of N mineralization and nitrification. Both tree species composition and season significantly influenced the soil dissolved organic carbon (DOC) and nitrogen (DON). N-fixing Acacia crassicarpa monoculture had the highest DON, and 10-mixed species plantation had the highest DOC. The lowest DOC and DON concentrations were both observed in Eucalyptus urophylla monoculture. The tree species composition also significantly affected net N mineralization rates. The highest rate of net N mineralization was found in A. crassicarpa monoculture, which was over twice than that in Castanopsis hystrix monoculture. The annual net N mineralization rates of 10-mixed and 30-mixed plantations were similar as that of N-fixing monoculture. Since mixed plantations have good performance in increasing soil DOC, DON, N mineralization and plant biodiversity, we recommend that mixed species plantations should be used as a sustainable approach for the restoration of degraded land in southern China.

Reforestation in southern China: revisiting soil N mineralization and nitrification after 8 years restoration.

PubMed

Mo, Qifeng; Li, Zhi'an; Zhu, Weixing; Zou, Bi; Li, Yingwen; Yu, Shiqin; Ding, Yongzhen; Chen, Yao; Li, Xiaobo; Wang, Faming

2016-01-22

Nitrogen availability and tree species selection play important roles in reforestation. However, long-term field studies on the effects and mechanisms of tree species composition on N transformation are very limited. Eight years after tree seedlings were planted in a field experiment, we revisited the site and tested how tree species composition affects the dynamics of N mineralization and nitrification. Both tree species composition and season significantly influenced the soil dissolved organic carbon (DOC) and nitrogen (DON). N-fixing Acacia crassicarpa monoculture had the highest DON, and 10-mixed species plantation had the highest DOC. The lowest DOC and DON concentrations were both observed in Eucalyptus urophylla monoculture. The tree species composition also significantly affected net N mineralization rates. The highest rate of net N mineralization was found in A. crassicarpa monoculture, which was over twice than that in Castanopsis hystrix monoculture. The annual net N mineralization rates of 10-mixed and 30-mixed plantations were similar as that of N-fixing monoculture. Since mixed plantations have good performance in increasing soil DOC, DON, N mineralization and plant biodiversity, we recommend that mixed species plantations should be used as a sustainable approach for the restoration of degraded land in southern China.

Mercury and organic carbon dynamics during runoff episodes from a northeastern USA watershed

USGS Publications Warehouse

Schuster, P.F.; Shanley, J.B.; Marvin-DiPasquale, M.; Reddy, M.M.; Aiken, G.R.; Roth, D.A.; Taylor, Howard E.; Krabbenhoft, D.P.; DeWild, J.F.

2008-01-01

Mercury and organic carbon concentrations vary dynamically in streamwater at the Sleepers River Research Watershed in Vermont, USA. Total mercury (THg) concentrations ranged from 0.53 to 93.8 ng/L during a 3-year period of study. The highest mercury (Hg) concentrations occurred slightly before peak flows and were associated with the highest organic carbon (OC) concentrations. Dissolved Hg (DHg) was the dominant form in the upland catchments; particulate Hg (PHg) dominated in the lowland catchments. The concentration of hydrophobic acid (HPOA), the major component of dissolved organic carbon (DOC), explained 41-98% of the variability of DHg concentration while DOC flux explained 68-85% of the variability in DHg flux, indicating both quality and quantity of the DOC substantially influenced the transport and fate of DHg. Particulate organic carbon (POC) concentrations explained 50% of the PHg variability, indicating that POC is an important transport mechanism for PHg. Despite available sources of DHg and wetlands in the upland catchments, dissolved methylmercury (DmeHg) concentrations in streamwaters were below detection limit (0.04 ng/L). PHg and particulate methylmercury (PmeHg) had a strong positive correlation (r 2 = 0.84, p < 0.0001), suggesting a common source; likely in-stream or near-stream POC eroded or re-suspended during spring snowmelt and summer storms. Ratios of PmeHg to THg were low and fairly constant despite an apparent higher methylmercury (meHg) production potential in the summer. Methylmercury production in soils and stream sediments was below detection during snowmelt in April and highest in stream sediments (compared to forest and wetland soils) sampled in July. Using the watershed approach, the correlation of the percent of wetland cover to TmeHg concentrations in streamwater indicates that poorly drained wetland soils are a source of meHg and the relatively high concentrations found in stream surface sediments in July indicate these zones are a meHg sink. ?? 2007 Springer Science+Business Media B.V.

A global hotspot for dissolved organic carbon in hypermaritime watersheds of coastal British Columbia

NASA Astrophysics Data System (ADS)

Oliver, Allison A.; Tank, Suzanne E.; Giesbrecht, Ian; Korver, Maartje C.; Floyd, William C.; Sanborn, Paul; Bulmer, Chuck; Lertzman, Ken P.

2017-08-01

The perhumid region of the coastal temperate rainforest (CTR) of Pacific North America is one of the wettest places on Earth and contains numerous small catchments that discharge freshwater and high concentrations of dissolved organic carbon (DOC) directly to the coastal ocean. However, empirical data on the flux and composition of DOC exported from these watersheds are scarce. We established monitoring stations at the outlets of seven catchments on Calvert and Hecate islands, British Columbia, which represent the rain-dominated hypermaritime region of the perhumid CTR. Over several years, we measured stream discharge, stream water DOC concentration, and stream water dissolved organic-matter (DOM) composition. Discharge and DOC concentrations were used to calculate DOC fluxes and yields, and DOM composition was characterized using absorbance and fluorescence spectroscopy with parallel factor analysis (PARAFAC). The areal estimate of annual DOC yield in water year 2015 was 33.3 Mg C km-2 yr-1, with individual watersheds ranging from an average of 24.1 to 37.7 Mg C km-2 yr-1. This represents some of the highest DOC yields to be measured at the coastal margin. We observed seasonality in the quantity and composition of exports, with the majority of DOC export occurring during the extended wet period (September-April). Stream flow from catchments reacted quickly to rain inputs, resulting in rapid export of relatively fresh, highly terrestrial-like DOM. DOC concentration and measures of DOM composition were related to stream discharge and stream temperature and correlated with watershed attributes, including the extent of lakes and wetlands, and the thickness of organic and mineral soil horizons. Our discovery of high DOC yields from these small catchments in the CTR is especially compelling as they deliver relatively fresh, highly terrestrial organic matter directly to the coastal ocean. Hypermaritime landscapes are common on the British Columbia coast, suggesting that this coastal margin may play an important role in the regional processing of carbon and in linking terrestrial carbon to marine ecosystems.

Hydrologic and forest management controls on DOC dynamics in the small watersheds of the H.J. Andrews Experimental Forest, OR

NASA Astrophysics Data System (ADS)

Lajtha, K.; Jones, J. A.

2016-12-01

Dissolved organic carbon (DOC) export from hillslopes to streams is an important component of the carbon cycle of a catchment and may be a critical source of energy for the aquatic food web in receiving waters. Using a long-term record of DOC and other dissolved nutrients and elements from paired watersheds from the H.J. Andrews Experimental Forest in Oregon, we explored hydrologic, climatic, and land-use controls on seasonal and inter-annual patterns of DOC flux in a seasonally dry ecosystem. Seasonal patterns of DOC flux demonstrated source limitations to DOC export, with DOC concentrations highest immediately following the first rains after a dry summer, and lowest after winter rains. In contrast, more geochemically-controlled elements showed simple dilution-concentration patterns with no seasonal hysteresis. Inter-annual patterns of DOC flux, however, did not provide evidence of source limitation, with DOC flux within a watershed tightly correlated to total discharge but not temperature. Among watersheds, forest harvest, even over 50 years ago, significantly reduced DOC flux but not fluxes of other elements including N; this response was linked to the loading of coarse woody debris to the forest floor. Chemical fingerprinting of DOC revealed that old-growth watersheds had higher fluxes of DOC characteristic of forest floor organic materials, likely delivered to streams through more surficial preferential flow pathways not subject to microbial alteration, respiration, or sorption losses. Taken together these results suggest that the biogeochemical composition of forested streams reflects both current hydrologic patterns and also processes that occurred many decades ago within the catchment.

Export of dissolved organic carbon from the Penobscot River basin in north-central Maine

USGS Publications Warehouse

Huntington, Thomas G.; Aiken, George R.

2013-01-01

Dissolved organic carbon (DOC) flux from the Penobscot River and its major tributaries in Maine was determined using continuous discharge measurements, discrete water sampling, and the LOADEST regression software. The average daily flux during 2004–2007 was 71 kg C ha−1 yr−1 (392 Mt C d−1), an amount larger than measured in most northern temperate and boreal rivers. Distinct seasonal variation was observed in the relation between concentration and discharge (C–Q). During June through December (summer/fall), there was a relatively steep positive C–Q relation where concentration increased by a factor of 2–3 over the approximately 20-fold range of observed stream discharge for the Penobscot River near Eddington, Maine. In contrast, during January through May (winter/spring), DOC concentration did not increase with increasing discharge. In addition, we observed a major shift in the C–Q between 2004–2005 and 2006–2007, apparently resulting from unprecedented rainfall, runoff, and soil flushing beginning in late fall 2005. The relative contribution to the total Penobscot River basin DOC flux from each tributary varied dramatically by season, reflecting the role of large regulated reservoirs in certain basins. DOC concentration and flux per unit watershed area were highest in tributaries containing the largest areas in palustrine wetlands. Tributary DOC concentration and flux was positively correlated to percentage wetland area. Climatic or environmental changes that influence the magnitude or timing of river discharge or the abundance of wetlands will likely affect the export of DOC to the near-coastal ocean.

36 year trends in dissolved organic carbon export from Finnish rivers to the Baltic Sea.

PubMed

Räike, Antti; Kortelainen, Pirkko; Mattsson, Tuija; Thomas, David N

2012-10-01

Increasing dissolved organic carbon (DOC) concentrations in lakes, rivers and streams in northern mid latitudes have been widely reported during the last two decades, but relatively few studies have dealt with trends in DOC export. We studied the export of DOC from Finnish rivers to the Baltic Sea between 1975 and 2010, and estimated trends in DOC fluxes (both flow normalised and non-normalised). The study encompassed the whole Finnish Baltic Sea catchment area (301,000 km(2)) covering major land use patterns in the boreal zone. Finnish rivers exported annually over 900,000 t DOC to the Baltic Sea, and the mean area specific export was 3.5 t km(-2). The highest export (7.3t km(-2)) was measured in peat dominated catchments, whereas catchments rich in lakes had the lowest export (2.2 t km(-2)). Inter-annual variation in DOC export was high and controlled mainly by hydrology. There was no overall trend in the annual water flow, although winter flow increased in northern Finland over 36 years. Despite the numerous studies showing increases in DOC concentrations in streams and rivers in the northern hemisphere, we could not find any evidence of increases in DOC export to the northern Baltic Sea from Finnish catchments since 1975. Copyright © 2012 Elsevier B.V. All rights reserved.

Organic Matter in Rivers: The Crossroads between Climate and Water Quality

DOE Office of Scientific and Technical Information (OSTI.GOV)

Davisson, M L

2001-04-27

All surface waters in the world contain dissolved organic matter and its concentration depends on climate and vegetation. Dissolved organic carbon (DOC) is ten times higher in wetlands and swamps than in surface water of arctic, alpine, or arid climate. Climates of high ecosystem productivity (i.e., tropics) typically have soils with low organic carbon storage, but drain high dissolved organic loads to rivers. Regions with lower productivity (e.g. grasslands) typically have high soil carbon storage while adjacent rivers have high DOC contents. Most DOC in a free-flowing river is derived from leaching vegetation and soil organic matter, whereas in dammedmore » rivers algae may comprise a significant portion. Water chemistry and oxygen-18 abundance of river water, along with radiocarbon and carbon-13 isotope abundance measurements of DOC were used to distinguish water and water quality sources in the Missouri River watershed. Drinking water for the City of St. Louis incorporates these different sources, and its water quality depends mostly on whether runoff is derived from the upper or the lower watershed, with the lower watershed contributing water with the highest DOC. During drinking water chlorination, DOC forms carcinogenic by-products in proportion to the amount of DOC present. This has recently led the USEPA to propose federal regulation standards. Restoration of natural riparian habitat such as wetlands will likely increase DOC concentrations in river water.« less

Reforestation in southern China: revisiting soil N mineralization and nitrification after 8 years restoration

PubMed Central

Mo, Qifeng; Li, Zhi’an; Zhu, Weixing; Zou, Bi; Li, Yingwen; Yu, Shiqin; Ding, Yongzhen; Chen, Yao; Li, Xiaobo; Wang, Faming

2016-01-01

Nitrogen availability and tree species selection play important roles in reforestation. However, long-term field studies on the effects and mechanisms of tree species composition on N transformation are very limited. Eight years after tree seedlings were planted in a field experiment, we revisited the site and tested how tree species composition affects the dynamics of N mineralization and nitrification. Both tree species composition and season significantly influenced the soil dissolved organic carbon (DOC) and nitrogen (DON). N-fixing Acacia crassicarpa monoculture had the highest DON, and 10-mixed species plantation had the highest DOC. The lowest DOC and DON concentrations were both observed in Eucalyptus urophylla monoculture. The tree species composition also significantly affected net N mineralization rates. The highest rate of net N mineralization was found in A. crassicarpa monoculture, which was over twice than that in Castanopsis hystrix monoculture. The annual net N mineralization rates of 10-mixed and 30-mixed plantations were similar as that of N-fixing monoculture. Since mixed plantations have good performance in increasing soil DOC, DON, N mineralization and plant biodiversity, we recommend that mixed species plantations should be used as a sustainable approach for the restoration of degraded land in southern China. PMID:26794649

Pushing Boreal Headwaters: Responses of Dissolved Organic Carbon to Increased Hydro-Meteorological Forcing by Forest Harvesting

NASA Astrophysics Data System (ADS)

Schelker, J.; Grabs, T. J.; Bishop, K. H.; Laudon, H.

2012-12-01

Concentrations of dissolved organic carbon (DOC) in stream water show large variations as a response to disturbances such as forestry operations. We used a paired catchment experiment in northern Sweden which shows well quantified increases of DOC concentrations and C-exports as a result of forest harvesting. To identify the drivers of these increases, a physically-based process model (Riparian Flow Integration Model, RIM) was used to inversely simulate the DOC availability in the peat-rich riparian soils of the catchments. DOC availability in soils followed a seasonal signal paralleling the seasonality of soil-temperatures (min: February; max: August) during 2005-2011. Further, high-frequency event sampling of DOC during spring and summer seasons of 2007, 2008 and 2009, respectively, revealed that event size acted as a secondary control of DOC in streams: Spring snowmelt events (as well as one major event in 2009) showed clockwise hysteresis, whereas minor runoff episodes during summer (when DOC availability in soils was highest) were characterized by a counterclockwise behavior. The higher hydro-meteorological forcing consisting of increases of soil temperature and soil moisture after the forest removal governed additional increases in DOC availability in soils. The higher DOC concentrations observed in streams after forest harvesting can therefore be ascribed to i) the increased climatic forcing comprising higher water flows through riparian soils, ii) increased soil temperatures and soil moisture, respectively, favoring an increased production of DOC, and iii) additional variation by event size. Overall these results underline the large impact of forestry operations on stream water quality as well as DOC exports leaving managed boreal forests. Simulated and measured soil water TOC concentration profiles within the three Balsjö catchments (CC-4 = clear-cut with 67% harvest; NO-5 = 35% harvest; NR-7 = northern reference). The simulated curves represent the inversely modeled soil profiles using the average f-parameter calculated for August 2009 for each catchment. Measured values represent TOC concentrations of soil water sampled in mid August 2009. Sample numbers (soil depth in bracket) are given as: n (-0.2m) = 16; n (-0.6m) = 17; n (-0.9m) = 15. Horizontal whiskers indicate the standard deviation of measured values for each soil depth.

Ancient low–molecular-weight organic acids in permafrost fuel rapid carbon dioxide production upon thaw

USGS Publications Warehouse

Drake, Travis W.; Wickland, Kimberly P.; Spencer, Robert G. M.; McKnight, Diane M.; Striegl, Robert G.

2015-01-01

Northern permafrost soils store a vast reservoir of carbon, nearly twice that of the present atmosphere. Current and projected climate warming threatens widespread thaw of these frozen, organic carbon (OC)-rich soils. Upon thaw, mobilized permafrost OC in dissolved and particulate forms can enter streams and rivers, which are important processors of OC and conduits for carbon dioxide (CO2) to the atmosphere. Here, we demonstrate that ancient dissolved organic carbon (DOC) leached from 35,800 y B.P. permafrost soils is rapidly mineralized to CO2. During 200-h experiments in a novel high–temporal-resolution bioreactor, DOC concentration decreased by an average of 53%, fueling a more than sevenfold increase in dissolved inorganic carbon (DIC) concentration. Eighty-seven percent of the DOC loss to microbial uptake was derived from the low–molecular-weight (LMW) organic acids acetate and butyrate. To our knowledge, our study is the first to directly quantify high CO2 production rates from permafrost-derived LMW DOC mineralization. The observed DOC loss rates are among the highest reported for permafrost carbon and demonstrate the potential importance of LMW DOC in driving the rapid metabolism of Pleistocene-age permafrost carbon upon thaw and the outgassing of CO2 to the atmosphere by soils and nearby inland waters.

Ancient low-molecular-weight organic acids in permafrost fuel rapid carbon dioxide production upon thaw.

PubMed

Drake, Travis W; Wickland, Kimberly P; Spencer, Robert G M; McKnight, Diane M; Striegl, Robert G

2015-11-10

Northern permafrost soils store a vast reservoir of carbon, nearly twice that of the present atmosphere. Current and projected climate warming threatens widespread thaw of these frozen, organic carbon (OC)-rich soils. Upon thaw, mobilized permafrost OC in dissolved and particulate forms can enter streams and rivers, which are important processors of OC and conduits for carbon dioxide (CO2) to the atmosphere. Here, we demonstrate that ancient dissolved organic carbon (DOC) leached from 35,800 y B.P. permafrost soils is rapidly mineralized to CO2. During 200-h experiments in a novel high-temporal-resolution bioreactor, DOC concentration decreased by an average of 53%, fueling a more than sevenfold increase in dissolved inorganic carbon (DIC) concentration. Eighty-seven percent of the DOC loss to microbial uptake was derived from the low-molecular-weight (LMW) organic acids acetate and butyrate. To our knowledge, our study is the first to directly quantify high CO2 production rates from permafrost-derived LMW DOC mineralization. The observed DOC loss rates are among the highest reported for permafrost carbon and demonstrate the potential importance of LMW DOC in driving the rapid metabolism of Pleistocene-age permafrost carbon upon thaw and the outgassing of CO2 to the atmosphere by soils and nearby inland waters.

Ancient low–molecular-weight organic acids in permafrost fuel rapid carbon dioxide production upon thaw

PubMed Central

Drake, Travis W.; Wickland, Kimberly P.; Spencer, Robert G. M.; McKnight, Diane M.; Striegl, Robert G.

2015-01-01

Northern permafrost soils store a vast reservoir of carbon, nearly twice that of the present atmosphere. Current and projected climate warming threatens widespread thaw of these frozen, organic carbon (OC)-rich soils. Upon thaw, mobilized permafrost OC in dissolved and particulate forms can enter streams and rivers, which are important processors of OC and conduits for carbon dioxide (CO2) to the atmosphere. Here, we demonstrate that ancient dissolved organic carbon (DOC) leached from 35,800 y B.P. permafrost soils is rapidly mineralized to CO2. During 200-h experiments in a novel high–temporal-resolution bioreactor, DOC concentration decreased by an average of 53%, fueling a more than sevenfold increase in dissolved inorganic carbon (DIC) concentration. Eighty-seven percent of the DOC loss to microbial uptake was derived from the low–molecular-weight (LMW) organic acids acetate and butyrate. To our knowledge, our study is the first to directly quantify high CO2 production rates from permafrost-derived LMW DOC mineralization. The observed DOC loss rates are among the highest reported for permafrost carbon and demonstrate the potential importance of LMW DOC in driving the rapid metabolism of Pleistocene-age permafrost carbon upon thaw and the outgassing of CO2 to the atmosphere by soils and nearby inland waters. PMID:26504243

Fluctuations of dissolved organic matter in river used for drinking water and impacts on conventional treatment plant performance.

PubMed

Volk, Christian; Kaplan, Louis A; Robinson, Jeff; Johnson, Bruce; Wood, Larry; Zhu, Hai Wei; LeChevallier, Mark

2005-06-01

Natural organic matter (NOM) in drinking water supplies can provide precursors for disinfectant byproducts, molecules that impact taste and odors, compounds that influence the efficacy of treatment, and other compounds that are a source of energy and carbon for the regrowth of microorganisms during distribution. NOM, measured as dissolved organic carbon (DOC), was monitored daily in the White River and the Indiana-American water treatment plant over 22 months. Other parameters were either measured daily (UV-absorbance, alkalinity, color, temperature) or continuously (turbidity, pH, and discharge) and used with stepwise linear regressions to predict DOC concentrations. The predictive models were validated with monthly samples of the river water and treatment plant effluent taken over a 2-year period after the daily monitoring had ended. Biodegradable DOC (BDOC) concentrations were measured in the river water and plant effluent twice monthly for 18 months. The BDOC measurements, along with measurements of humic and carbohydrate constituents within the DOC and BDOC pools, revealed that carbohydrates were the organic fraction with the highest percent removal during treatment, followed by BDOC, humic substances, and refractory DOC.

DOM composition in an agricultural watershed: assessing patterns and variability in the context of spatial scales

USGS Publications Warehouse

Hernes, Peter J.; Spencer, Robert G. M.; Dyda, Rachel Y.; Pellerin, Brian A.; Bachand, Philip A. M.; Bergamaschi, Brian A.

2013-01-01

Willow Slough, a seasonally irrigated agricultural watershed in the Sacramento River valley, California, was sampled synoptically in order to investigate the extent to which dissolved organic carbon (DOC) concentrations and compositions from throughout the catchment are represented at the mouth. DOC concentrations ranged from 1.8 to 13.9 mg L−1, with the lowest values in headwater 1st and 2nd order streams, and the highest values associated with flood irrigation. Carbon-normalized vanillyl phenols varied from 0.05 to 0.67 mg 100 mg OC−1 (0.37 mean), indicative of considerable contributions from vascular plants. DOC concentrations and compositions at the mouth appear to be primarily influenced by land use (agriculture) in the lower reaches, and therefore very little of the headwater chemistry (1st and 2nd order streams) can be discerned from the chemistry at or near the mouth (3rd and 4th order streams), indicating the need for synoptic sampling to capture the breadth of organic carbon cycling within a catchment. Field sampling during irrigation showed the large impact that flood irrigation can have on DOC concentrations and compositions, likely a primary cause of significantly elevated Willow Slough DOC concentrations during the summer irrigation season. Optical proxies exhibited varying degrees of correlation with chemical measurements, with strongest relationships to DOC and dissolved lignin (r2 = 0.95 and 0.73, respectively) and weaker relationships to carbon-normalized lignin yields and C:V (r2 from 0.31 to 0.42). Demonstrating the importance of matching scale to processes, we found no relationship between dissolved lignin concentrations and total suspended sediments (TSS) across all sites, in contrast to the strong relationship observed in weekly samples at the mouth. As DOC concentrations and compositions at the mouth of Willow Slough are closely tied to anthropogenic activities within the catchment, future changes in land-use driven by climate change, water availability, and economic pressures on crop types will also bring about changes in the overall biogeochemistry.

Hydro-climatic control of stream water dissolved organic carbon (DOC) across northern catchments within the North-Watch program

NASA Astrophysics Data System (ADS)

Laudon, Hjalmar; Tetzlaff, Doerthe; Seibert, Jan; Soulsby, Chris; Carey, Sean; Buttle, Jim; McDonnell, Jeff; McGuire, Kevin; Caissie, Daniel; Shanley, Jamie

2010-05-01

There has been an increasing interest in understanding the regulating mechanisms of surface water dissolved organic carbon (DOC) the last decade. A majority of this recent work has been based on individual well characterized research catchments or on regional synoptic datasets combined with readily available landscape and climatic variables. However, as the production and transport of DOC primarily is a function of hydro-climatic conditions a better description of catchment hydrological functioning across large geographic regions would be favorable for moving the mechanistic understanding forward. To do this we report from a first assessment of catchment DOC within the international inter-catchment comparison program North-Watch (http://www.abdn.ac.uk/northwatch/). North-Watch includes long-term research catchments ranging from northern temperate regions to the boreal and sub-arctic biomes with the aim to better understand the variable hydrological and biogeochemical responses in Northern catchments to climate change. The North-Watch catchments are located in Sweden (Krycklan), Scotland (Mharcaidh, Girnock and Strontian), the US (Sleepers River and HJ Andrews) and Canada (Catamaran, Dorset and Wolf Creek). The annual average DOC concentration in the nine catchments investigated were directly linked to hydro-climatic influences (e.g. temperature, water storage) and landscape configuration. In general, the DOC concentration followed a parabolic shape with temperature, where the highest concentrations were found in the boreal and near boreal sites and with the lowest concentrations in the temperate and sub-arctic catchments. The between catchment variability in DOC concentration could also be explained by catchment water storage and amount of wetlands in the catchment. Whereas there is a mechanistic link between long-term climatic conditions and the areal coverage of wetlands, the total catchment storage of water is more strongly linked to topography, parent material and soil depth. The result from this analysis will serve as a conceptual framework for understanding biogeochemical response to environmental change across northern catchments. The next step in this work will be to include more detailed comparisons of the role catchment hydrological functioning for explaining the patterns and dynamics of catchment DOC of these northern watersheds.

Examining the interrelationship between DOC, bromide and chlorine dose on DBP formation in drinking water--a case study.

PubMed

Bond, Tom; Huang, Jin; Graham, Nigel J D; Templeton, Michael R

2014-02-01

During drinking water treatment aqueous chlorine and bromine compete to react with natural organic matter (NOM). Among the products of these reactions are potentially harmful halogenated disinfection by-products, notably four trihalomethanes (THM4) and nine haloacetic acids (HAAs). Previous research has concentrated on the role of bromide in chlorination reactions under conditions of a given NOM type and/or concentration. In this study different concentrations of dissolved organic carbon (DOC) from U.K. lowland water were reacted with varying amounts of bromide and chlorine in order to examine the interrelationship between the three reactants in the formation of THM4, dihaloacetic acids (DHAAs) and trihaloacetic acids (THAAs). Results showed that, in general, molar yields of THM4 increased with DOC, bromide and chlorine concentrations, although yields did fluctuate versus chlorine dose. In contrast both DHAA and THAA yields were mainly independent of changes in bromide and chlorine dose at low DOC (1 mg·L(-1)), but increased with chlorine dose at higher DOC concentrations (4 mg·L(-1)). Bromine substitution factors reached maxima of 0.80, 0.67 and 0.65 for the THM4, DHAAs and THAAs, respectively, at the highest bromide/chlorine ratio studied. These results suggest that THM4 formation kinetics depend on both oxidation and halogenation steps, whereas for DHAAs and THAAs oxidation steps are more important. Furthermore, they indicate that high bromide waters may prove more problematic for water utilities with respect to THM4 formation than for THAAs or DHAAs. While mass concentrations of all three groups increased in response to increased bromide incorporation, only the THMs also showed an increase in molar yield. Overall, the formation behaviour of DHAA and THAA was more similar than that of THM4 and THAA. © 2013.

Effects of ocean acidification on pelagic carbon fluxes in a mesocosm experiment

NASA Astrophysics Data System (ADS)

Spilling, Kristian; Schulz, Kai G.; Paul, Allanah J.; Boxhammer, Tim; Achterberg, Eric P.; Hornick, Thomas; Lischka, Silke; Stuhr, Annegret; Bermúdez, Rafael; Czerny, Jan; Crawfurd, Kate; Brussaard, Corina P. D.; Grossart, Hans-Peter; Riebesell, Ulf

2016-11-01

About a quarter of anthropogenic CO2 emissions are currently taken up by the oceans, decreasing seawater pH. We performed a mesocosm experiment in the Baltic Sea in order to investigate the consequences of increasing CO2 levels on pelagic carbon fluxes. A gradient of different CO2 scenarios, ranging from ambient ( ˜ 370 µatm) to high ( ˜ 1200 µatm), were set up in mesocosm bags ( ˜ 55 m3). We determined standing stocks and temporal changes of total particulate carbon (TPC), dissolved organic carbon (DOC), dissolved inorganic carbon (DIC), and particulate organic carbon (POC) of specific plankton groups. We also measured carbon flux via CO2 exchange with the atmosphere and sedimentation (export), and biological rate measurements of primary production, bacterial production, and total respiration. The experiment lasted for 44 days and was divided into three different phases (I: t0-t16; II: t17-t30; III: t31-t43). Pools of TPC, DOC, and DIC were approximately 420, 7200, and 25 200 mmol C m-2 at the start of the experiment, and the initial CO2 additions increased the DIC pool by ˜ 7 % in the highest CO2 treatment. Overall, there was a decrease in TPC and increase of DOC over the course of the experiment. The decrease in TPC was lower, and increase in DOC higher, in treatments with added CO2. During phase I the estimated gross primary production (GPP) was ˜ 100 mmol C m-2 day-1, from which 75-95 % was respired, ˜ 1 % ended up in the TPC (including export), and 5-25 % was added to the DOC pool. During phase II, the respiration loss increased to ˜ 100 % of GPP at the ambient CO2 concentration, whereas respiration was lower (85-95 % of GPP) in the highest CO2 treatment. Bacterial production was ˜ 30 % lower, on average, at the highest CO2 concentration than in the controls during phases II and III. This resulted in a higher accumulation of DOC and lower reduction in the TPC pool in the elevated CO2 treatments at the end of phase II extending throughout phase III. The "extra" organic carbon at high CO2 remained fixed in an increasing biomass of small-sized plankton and in the DOC pool, and did not transfer into large, sinking aggregates. Our results revealed a clear effect of increasing CO2 on the carbon budget and mineralization, in particular under nutrient limited conditions. Lower carbon loss processes (respiration and bacterial remineralization) at elevated CO2 levels resulted in higher TPC and DOC pools than ambient CO2 concentration. These results highlight the importance of addressing not only net changes in carbon standing stocks but also carbon fluxes and budgets to better disentangle the effects of ocean acidification.

Spatial patterns of DOC concentration and DOM optical properties in a Brazilian tropical river-wetland system

NASA Astrophysics Data System (ADS)

Dalmagro, Higo J.; Johnson, Mark S.; de Musis, Carlo R.; Lathuillière, Michael J.; Graesser, Jordan; Pinto-Júnior, Osvaldo B.; Couto, Eduardo G.

2017-08-01

The Cerrado (savanna) and Pantanal (wetland) biomes of Central Western Brazil have experienced significant development activity in recent decades, including extensive land cover conversion from natural ecosystems to agriculture and urban expansion. The Cuiabá River transects the Cerrado biome prior to inundating large areas of the Pantanal, creating one of the largest biodiversity hot spots in the world. We measured dissolved organic carbon (DOC) and the optical absorbance and fluorescence properties of dissolved organic matter (DOM) from 40 sampling locations spanning Cerrado and Pantanal biomes during wet and dry seasons. In the upper, more agricultural region of the basin, DOC concentrations were highest in the rainy season with more aromatic and humified DOM. In contrast, DOC concentrations and DOM optical properties were more uniform for the more urbanized middle region of the basin between wet and dry seasons, as well as across sample locations. In the lower region of the basin, wet season connectivity between the river and the Pantanal floodplain led to high DOC concentrations, a fourfold increase in humification index (HIX) (an indicator of DOM humification), and a 50% reduction in the spectral slope (SR). Basin-wide, wet season values for SR, HIX, and FI (fluorescence index) indicated an increasing representation of terrestrially derived DOM that was more humified. Parallel factor analysis identified two terrestrially derived components (C1 and C2) representing 77% of total fluorescing DOM (fDOM). A third, protein-like fDOM component increased markedly during the wet season within the more urban-impacted region.

Spatiotemporal variation of dissolved carbohydrates and amino acids in Jiaozhou Bay, China

NASA Astrophysics Data System (ADS)

Shi, Di; Yang, Guipeng; Sun, Yan; Wu, Guanwei

2017-03-01

Surface seawater samples were collected from Jiaozhou Bay, China, during six cruises (March-May 2010, September-November 2010) to study the distribution of dissolved organic matter including dissolved organic carbon (DOC), total dissolved carbohydrates, namely monosaccharides (MCHO) and polysaccharides (PCHO) and total hydrolysable amino acids. These included dissolved free amino acids (DFAA) and combined amino acids (DCAA). The goal was to investigate possible relationships between these dissolved organic compounds and environmental parameters. During spring, the concentrations of MCHO and PCHO were 9.6 (2.8-22.6) and 11.0 (2.9-42.5) μmol C/L, respectively. In autumn, MCHO and PCHO were 9.1 (2.6-27.0) and 10.8 (2.4-25.6) μmol C/L, respectively. The spring concentrations of DFAA and DCAA were 1.7 (1.1-4.1) and 7.6 (1.1-31.0) μmol C/L, respectively, while in autumn, DFAA and DCAA were 2.3 (1.1-8.0) and 3.3 (0.6-7.2) μmol C/L, respectively. Among these compounds, the concentrations of PCHO were the highest, accounting for nearly a quarter of the DOC, followed by MCHO, DCAA and DFAA. The concentrations of the organic compounds exhibited a decreasing trend from the coastal to the central regions of the bay. A negative correlation between concentrations of DOC and salinity in each cruise suggested that riverine inputs around the bay have an important impact on the distribution of DOC in the surface water. A significant positive correlation was found between DOC and total bacteria count in spring and autumn, suggesting bacteria play an important role in the marine carbon cycle.

Dissolved organic carbon in soil solution of peat-moorsh soils on Kuwasy Mire

NASA Astrophysics Data System (ADS)

Jaszczyński, J.; Sapek, A.

2009-04-01

Key words: peat-moorsh soils, soil solution, dissolved organic carbon (DOC), temperature of soil, redox potential. The objective this study was the dissolved organic carbon concentration (DOC) in soil solution on the background of soil temperature, moisture and redox potential. The investigations were localized on the area of drained and agricultural used Kuwasy Mire, which are situated in the middle basin of Biebrza River, in North-East Poland. Research point was placed on a low peat soil of 110 cm depth managed as extensive grassland. The soil was recognized as peat-moorsh with the second degree of the moorshing process (with 20 cm of moorsh layer). The ceramic suction cups were installed in three replications at 30 cm depth of soil profile. The soil solution was continuously sampled by pomp of the automatic field station. The successive samples comprised of solution collected at the intervals of 21 days. Simultaneously, at the 20, 30 and 40 cm soil depths the measurements of temperature and determination of soil moisture and redox potential were made automatically. The mean twenty-four hours data were collected. The concentrations of DOC were determined by means of the flow colorimeter using the Skalar standard methods. Presented observations were made in 2001-2006. Mean DOC concentration in soil solution was 66 mg.dm-3 within all research period. A significant positive correlation between studied compound concentration and temperature of soil at 30 cm depth was observed; (correlation coefficient - r=0.55, number of samples - n=87). The highest DOC concentrations were observed during the season from July to October, when also a lower ground water level occurred. The DOC concentration in soil solution showed as well a significant correlation with the soil redox potential at 20 cm level. On this depth of describing soil profile a frontier layer between moorshing layer and peat has been existed. This layer is the potentially most active in the respect to biochemical transformation. On the other hand it wasn't possible to shown dependences on the DOC concentration from soil moisture. That probably results from a huge water-holding capacity of these type of peat soils, which are keeping a high moisture content even at a long time after decreasing of the groundwater table.

Does quinone or phenol enrichment of humic substances alter the primary compound from a non-algicidal to an algicidal preparation?

PubMed

Bährs, Hanno; Menzel, Ralph; Kubsch, Georg; Stösser, Reinhardt; Putschew, Anke; Heinze, Tobias; Steinberg, Christian E W

2012-06-01

Dissolved organic matter (DOM) has been shown to affect phytoplankton species directly. These interactions largely depend on the origin and molecular size of DOM and are different in prokaryotes and eukaryotes. In a preceding study, however, two humic substance preparations did not adversely affect coccal green algae or cyanobacterial growth even at high concentrations of dissolved organic carbon (DOC). These results contradicted previous findings, showing a clear, negative response of different phototrophs to much lower DOC concentrations. To test whether or not at least defined building blocks of humic substances (HSs) are effective algicidal structures, we enriched two humic preparations with hydroquinone and p-benzoquinone, respectively, and exposed two different green algae, Pseudokirchneriella subcapitata and Monoraphidium braunii, and two cyanobacterial species, Synechocystis sp. and Microcystis aeruginosa, to the unmodified and enriched HSs. As response variables, growth rates in terms of biomass increase, chlorophyll-a content, and photosynthetic yield were measured. The highest concentration (4.17 mM DOC) of the modified HSs clearly inhibited growth; the cyanobacterial species were much more sensitive than the green algal species. However, realistic ecological concentrations did not adversely affect growth. Aerating the exposure solution for 24 h strongly reduced the inhibitory effect of the modified HSs. The algicidal effect was obviously caused by monomers and not by polymerised high molecular weight HSs themselves. Furthermore, the maximum quantum yield (Φ PSII max) was stimulated in the green algal species by low and medium DOC concentrations, but reduced in the cyanobacterial species upon exposure to higher HS concentrations. The quinone- and phenol-enriched HSs only showed algicidal activity at high concentrations of 4.17 mM DOC and lost their effects over time, presumably by oxidation and subsequent polymerisation. This study confirms that the applied humic substances themselves are not effective algicides even if enriched in effective structures. Copyright © 2012 Elsevier Ltd. All rights reserved.

Antibiotics in the surface water of the Yangtze Estuary: occurrence, distribution and risk assessment.

PubMed

Yan, Caixia; Yang, Yi; Zhou, Junliang; Liu, Min; Nie, Minghua; Shi, Hao; Gu, Lijun

2013-04-01

The occurrence and distribution of five groups of antibiotics were investigated in the surface water of Yangtze Estuary over four seasons. Of the 20 antibiotics, only sulfamerazine was not detected at all sampling sites, indicating widespread occurrence of antibiotic residues in the study area. Detection frequencies and concentrations of antibiotics were generally higher in January, indicating that low flow conditions and low temperature might enhance the persistence of antibiotics in water. Antibiotic levels varied with location, with the highest concentrations being observed around river discharge and sewage outfall. Furthermore, a positive correlation between total antibiotic and DOC concentrations revealed the significant role played by DOC. Risk assessment based on single compound exposure showed that sulfapyridine and sulfamethoxazole could cause medium risk to daphnid in the Yangtze Estuary. Copyright © 2012 Elsevier Ltd. All rights reserved.

Stormflow influence on nutrient dynamics in micro-catchments under contrasting land use in the Cerrado and Amazon Biomes, Brazil

NASA Astrophysics Data System (ADS)

Edelmann, Katharina; Nóbrega, Rodolfo L. B.; Gerold, Gerhard

2017-04-01

The Amazon and Cerrado biomes in Brazil have been under intense land-use change during the past few decades. The conversion of native vegetation to pastures and croplands has caused impacts on hydrological processes in these biomes, resulting in increased streamflow and nutrient fluxes. Our aim was to compare the nutrient dynamics during stormflow events in two pairs of adjacent micro-catchments with similar physical characteristics under contrasting land use, i.e. native vegetation (rainforest or cerrado) and pasture. One pair of catchments was located in the Amazon and the other in the Cerrado, both on the Amazon Agricultural Frontier in the Brazilian states of Mato Grosso and Pará. We collected hydrological and hydrochemical data on 50 stormflow events on a sub-hourly resolution during the wet seasons of 2013 and 2014. We compared the dynamics of total inorganic carbon (TIC), total organic carbon (TOC), dissolved organic carbon (DOC), nitrate (NO3), calcium (Ca), potassium (K), and magnesium (Mg) in different hydrograph parts, i.e. rising limb, peak and recession limb, between the catchments within the same biome. For the Cerrado biome, our findings show that the nutrient concentrations in the stormflows were higher in the pasture catchment than in the cerrado catchment. In the Amazon biome, we found an inverse relationship with higher concentrations in the forest catchment than in the pasture catchment, except for TIC and K. Most nutrients in the cerrado catchment had the highest concentrations in the rising limb. Mg, however, reached highest concentrations during peak discharge, and lowest in the recession limb. In the adjacent pasture catchment, in contrast, the highest nutrient concentrations were observed during the peak discharge (TIC, TOC, Ca) or the recession limb (DOC, NO3, K, Mg) with lowest in the rising limb, except for NO3, which showed the lowest concentrations during peak discharge. In the Amazon forest catchment, the peak discharge showed the highest nutrient concentrations, while concentrations in the recession limb were higher than in the rising limb. We also found that in this catchment K concentrations were lower in the recession limb than in the rising limb. In the Amazonian pasture catchment, the peak discharge showed the greatest concentrations for TIC, TOC, and Ca, and the rising limb the lowest. DOC and NO3 concentrations in this catchment were the highest in the rising and were lowest in peak discharge, while K increased over time. Based on that, we conclude that stormflow is an important driver of nutrients fluxes due to land-use change on the Amazon Agricultural Frontier, with significant increases and distinguished dynamics during the storm events, and higher nutrient concentrations in the catchments with pastures than in the ones with native vegetation, especially for TIC and K.

Mercury and Dissolved Organic Matter Dynamics During Snowmelt in the Upper Provo River, Utah, USA

NASA Astrophysics Data System (ADS)

Packer, B. N.; Carling, G. T.; Nelson, S.; Aanderud, Z.; Shepherd Barkdull, N.; Gabor, R. S.

2017-12-01

Mercury (Hg) is deposited to mountains by atmospheric deposition and mobilized during snowmelt runoff, leading to Hg contamination in otherwise pristine watersheds. Mercury is typically transported with dissolved organic matter (DOM) from soils to streams and lakes. This study focused on Hg and DOM dynamics in the snowmelt-dominated upper Provo River watershed, northern Utah, USA. We sampled Hg, dissolved organic carbon (DOC) concentrations, and DOM fluorescence in river water, snowpack, and ephemeral streams over four years from 2014-2017 to investigate Hg transport mechanisms. During the snowmelt season (April through June), Hg concentrations typically increased from 1 to 8 ng/L showing a strong positive correlation with DOC. The dissolved Hg fraction was dominant in the river, averaging 75% of total Hg concentrations, suggesting that DOC is more important for transport than suspended particulate matter. Ephemeral channels, which represent shallow flow paths with strong interactions with soils, had the highest Hg (>10 ng/L) and DOC (>10 mg/L) concentrations, suggesting a soil water source of Hg and organic matter. Fluorescence spectroscopy results showed important changes in DOM type and quality during the snowmelt season and the soil water flow paths are activated. Changes in DOM characteristics during snowmelt improve the understanding of Hg dynamics with organic matter and elucidate transport pathways from the soil surface, ephemeral channels and groundwater to the Provo River. This study has implications for understanding Hg sources and transport mechanisms in mountain watersheds.

Stormflow chemistry in the Santa Ana River below Prado Dam and at the diversion downstream from Imperial Highway, southern California, 1995-98

USGS Publications Warehouse

Izbicki, John A.; Mendez, Gregory O.; Burton, Carmen A.

2000-01-01

The Santa Ana River drains about 2,670 square miles of the densely populated coastal area of southern California, near Los Angeles. Almost all the flow in the river, more than 200,000 acre-feet annually, is diverted into ponds where it infiltrates and recharges underlying aquifers. About 2 million people are dependent on these aquifers for water supply. Stormflow in the Santa Ana River is considered a source of 'high-quality' water suitable for use as a source of ground-water recharge. To test this assumption, stormflow samples were collected at two locations--below Prado Dam and at the diversion point downstream from Imperial Highway--for 12 winter storms between 1995 and 1998. Nitrate concentrations decreased during stormflow from a median concentration of 7.8 milligrams per liter in base flow to concentrations less than 1 milligram per liter in some large storms. Concentrations of chemically reduced forms of nitrogen (nitrite, ammonia, and organic nitrogen) increased during stormflow and are the predominant forms of nitrogen in large stormflows. Dissolved organic carbon (DOC) concentrations increased from a median concentration of 4.6 milligrams per liter in base flow to more than 20 milligrams per liter in some stormflows. Concentrations of DOC were especially high during the first storm of the rainy season, and large increases in DOC concentrations were measured even as a result of small early season storms that did not cause large increases in streamflow. DOC present during early season stormflow had less ultraviolet absorbance at 254 nanometers (UV254 ) per unit of carbon than did DOC from late season stormflows. DOC in water held in storage behind Prado Dam had the highest UV254 absorbance per unit of carbon. Maximum pesticide concentrations in stormflow did not exceed U.S. Environmental Protection Agency Maximum Contaminant Levels. Most pesticide concentrations were less than 1 microgram per liter and less than the detection limits obtained using standard drinking water analyses. Increases in concentrations of pesticides such as diazinon, malathion, and chlorpyrifos in stormflow result from runoff from urban areas downstream from Prado Dam. In general, large late season stormflows have the most pesticide detections of all stormflows sampled. Concentrations of methyl tert-butyl ether (MTBE), a gasoline additive, during base flow were as high as 0.9 microgram per liter and concentrations decreased during stormflow. Like pesticides, the concentrations did not exceed the U.S. Environmental Protection Agency Maximum Contaminant Levels for MTBE.

Macronutrient status of UK groundwater: Nitrogen, phosphorus and organic carbon.

PubMed

Stuart, M E; Lapworth, D J

2016-12-01

Groundwater is a large, slowly changing pool of the macronutrients nitrogen (N), phosphorus (P) and dissolved organic carbon (DOC), with impacts on receptors, surface waters, dependent wetlands and coastal marine ecosystems. Sources of N to groundwater include fertilisers, animal wastes and septic effluents. N species are well-quantified in groundwater and NO 3 -N has a wide range of median values (0-12mg/L). The highest concentrations are in the Chalk of East Anglia and Humberside and the Permo-Triassic Sandstone (PTS) of Staffordshire. The highest concentrations of NH 4 -N are found in confined aquifers. N concentrations have increased with time peaking during the 1980s. Changes in practice have led to the reduction observed in rapidly-responding aquifers. For the Chalk, where the unsaturated zone is thick, improvements may not be seen for decades. P is less well-characterised in UK groundwater reflecting the lack of historical interest in groundwater P, although it can be significant in some aquifer matrices. Groundwater P concentrations are elevated in sandstone formations compared to other lithology and highest in the PTS of the Midlands and northern England (median values>50μg/L). Overall half of the aquifers studied in the UK have median TDP>50μg/L, with values of up to 100μg/L under some urban areas, such as Manchester and Liverpool as well as the Lee Valley. P concentrations in arable areas are variable (20-100μg/L), whereas under semi-natural conditions they are lower (20-50μg/L). There is little information on P trends in groundwater. Most DOC is derived from soils, playing an important part in redox processes. The aquifer matrix can contain high OC and contribute significantly to groundwater DOC. Median values range between 0.4 and 9mg/L, but rarely exceed 5mg/L, except in the Chalk of Yorkshire and Humberside and PTS of Liverpool which have long legacies of anthropogenic pollution. Copyright © 2016 The Authors. Published by Elsevier B.V. All rights reserved.

The Influence of Wetland Cover and Dissolved Organic Carbon on Mercury Export in Forest Landscapes, Northeastern USA

NASA Astrophysics Data System (ADS)

Dittman, J. A.; Shanley, J. B.; Driscoll, C. T.; Aiken, G.; Chalmers, A.; Towse, J.

2007-12-01

Mercury (Hg) contamination is widespread in remote areas of the northeastern USA. Atmospheric Hg is deposited on terrestrial uplands and subsequently mobilized to downstream aquatic ecosystems. We are investigating the fate of Hg deposited in forested watersheds by quantifying stream transport of Hg, and the interactions with dissolved and particulate organic matter. We hypothesize that the landscape characteristics controlling the production and mobility of organic matter will likewise control the mobility of Hg. This research was conducted at three sites in the Northeast that represent a range of hydrochemical conditions and span a range of wetland cover. Most stream export of Hg occurs at high flow; therefore we collected samples during snowmelt and storms. Mercury concentrations increase with discharge at all three sites; however the partitioning of Hg fractions (dissolved vs. particulate) differs among sites during high flow events. At the Hubbard Brook Experimental Forest, NH (watershed 6), there are no true wetlands and dissolved organic carbon (DOC) and total Hg (THg) concentrations, and suspended sediment concentration (SSC) (mean DOC = 3.1 mg C L-1; THg = 1.5 ng L-1; SSC < 50 mg L-1) are low even during the highest of flow events. At Sleepers River, VT (watershed 9), SSC can be elevated during events (SSC > 500 mg L-1), consequently the particulate Hg fraction can range as high as 95% of the THg concentration (mean particulate Hg concentration = 10.2 ng L- 1). At Archer Creek (Huntington Forest, NY), which has the greatest percent wetland cover (10%) of our three sites, DOC concentrations are high (mean DOC = 7.5 mg C L-1), while SSC are low (SSC < 10 mg L- 1). At Archer Creek, Hg is largely in the dissolved form (~75% of Hg) and strongly correlated with DOC (r2 = 0.90). The hydrophobic organic acid (HPOA) fraction of DOC is most effective at mobilizing Hg and is strongly correlated to Hg concentrations in stream water. This research suggests that high concentrations of Hg can be present in stream water from forest watersheds during high flow events, and that wetlands and suspended sediment favor Hg export. However, it is not clear to what degree this Hg is bioavailable for potential uptake by organisms in aquatic ecosystems following mobilization.

Estimated ultraviolet radiation doses in wetlands in six national parks

USGS Publications Warehouse

Diamond, S.A.; Trenham, P.C.; Adams, Michael J.; Hossack, B.R.; Knapp, R.A.; Stark, L.; Bradford, D.; Corn, P.S.; Czarnowski, K.; Brooks, P.D.; Fagre, D.B.; Breen, B.; Dentenbeck, N.E.; Tonnessen, K.

2005-01-01

Ultraviolet-B radiation (UV-B, 280–320-nm wavelengths) doses were estimated for 1024 wetlands in six national parks: Acadia (Acadia), Glacier (Glacier), Great Smoky Mountains (Smoky), Olympic (Olympic), Rocky Mountain (Rocky), and Sequoia/Kings Canyon (Sequoia). Estimates were made using ground-based UV-B data (Brewer spectrophotometers), solar radiation models, GIS tools, field characterization of vegetative features, and quantification of DOC concentration and spectral absorbance. UV-B dose estimates were made for the summer solstice, at a depth of 1 cm in each wetland. The mean dose across all wetlands and parks was 19.3 W-h m−2 (range of 3.4–32.1 W-h m−2). The mean dose was lowest in Acadia (13.7 W-h m−2) and highest in Rocky (24.4 W-h m−2). Doses were significantly different among all parks. These wetland doses correspond to UV-B flux of 125.0 μW cm−2 (range 21.4–194.7 μW cm−2) based on a day length, averaged among all parks, of 15.5 h. Dissolved organic carbon (DOC), a key determinant of water-column UV-B flux, ranged from 0.6 (analytical detection limit) to 36.7 mg C L−1 over all wetlands and parks, and reduced potential maximal UV-B doses at 1-cm depth by 1%–87 %. DOC concentration, as well as its effect on dose, was lowest in Sequoia and highest in Acadia (DOC was equivalent in Acadia, Glacier, and Rocky). Landscape reduction of potential maximal UV-B doses ranged from zero to 77% and was lowest in Sequoia. These regional differences in UV-B wetland dose illustrate the importance of considering all aspects of exposure in evaluating the potential impact of UV-B on aquatic organisms.

Effect of exchangeable cation concentration on sorption and desorption of dissolved organic carbon in saline soils.

PubMed

Setia, Raj; Rengasamy, Pichu; Marschner, Petra

2013-11-01

Sorption is a very important factor in stabilization of dissolved organic carbon (DOC) in soils and thus C sequestration. Saline soils have significant potential for C sequestration but little is known about the effect of type and concentration of cations on sorption and release of DOC in salt-affected soils. To close this knowledge gap, three batch sorption and desorption experiments were conducted using soils treated with solutions either low or high in salinity. In Experiment 1, salinity was developed with either NaCl or CaCl2 to obtain an electrical conductivity (EC) in a 1:5 soil: water extract (EC1:5) of 2 and 4 dS m(-1). In Experiments 2 and 3, NaCl and CaCl2 were added in various proportions (between 25 and 100%) to obtain an EC1:5 of 0.5 and 4 dS m(-1), respectively. At EC1:5 of 4 dS m(-1), the sorption of DOC (derived from wheat straw) was high even at a low proportion of added Ca(2+) and did not change with proportion of Ca added, but at EC1:5 of 0.5 dS m(-1) increasing proportion of Ca(2+) added increased DOC sorption. This can be explained by the differences in exchangeable Ca(2+) at the two salinity levels. At EC1:5 of 4 dS m(-1), the exchangeable Ca(2+) concentration did not increase beyond a proportion of 25% Ca(2+), whereas it increased with increasing Ca(2+) proportion in the treatments at EC1:5 of 0.5 dS m(-1). The DOC sorption was lowest with a proportion of 100% as Na(+). When Ca(2+) was added, DOC sorption was highest, but least was desorbed (with deionised water), thus sorption and desorption of added DOC were inversely related. The results of this study suggest that DOC sorption in salt-affected soils is mainly controlled by the levels of exchangeable Ca(2+) irrespective of the Ca(2+) concentration in the soil solution which has implications on carbon stabilization in salt-affected soils. Copyright © 2013 Elsevier B.V. All rights reserved.

Bacterial Abundance and Activity across Sites within Two Northern Wisconsin Sphagnum Bogs.

PubMed

Fisher; Graham; Graham

1998-11-01

Abstract Bacterial abundance, temperature, pH, and dissolved organic carbon (DOC) concentration were compared across surface sites within and between two northern Wisconsin Sphagnum peatlands over the summer seasons in 1995 and 1996. Sites of interest were the Sphagnum mat surface, the water-filled moat (lagg) at the bog margin, and the bog lake littoral zone. Significant differences in both bacterial populations and water chemistry were observed between sites. pH was highest in the lake and lowest in the mat at both bogs; the opposite was true for DOC. Large populations of bacteria were present in surface interstitial water from the mat; abundance in this site was consistently higher than in the moat or lake. Bacterial abundance also increased across sites of increasing DOC concentration and declining pH. Bacterial activities (rates of [3H]leucine incorporation) and growth in dilution cultures (with grazers removed) were also assessed in lake, moat, and mat sites. Results using these measures generally supported the trends observed in abundance, although high rates of [3H]leucine incorporation were recorded in the moat at one of the bogs. Our results indicate that bacterial populations in Sphagnum peatlands are not adversely affected by acidity, and that DOC may be more important than pH in determining bacterial abundance in these environments.

Dissolved organic matter composition of Arctic rivers: Linking permafrost and parent material to riverine carbon

USGS Publications Warehouse

O’Donnell, Jonathan A.; Aiken, George R.; Swanson, David K.; Santosh, Panda; Butler, Kenna D.; Baltensperger, Andrew P.

2016-01-01

Recent climate change in the Arctic is driving permafrost thaw, which has important implications for regional hydrology and global carbon dynamics. Permafrost is an important control on groundwater dynamics and the amount and chemical composition of dissolved organic matter (DOM) transported by high-latitude rivers. The consequences of permafrost thaw for riverine DOM dynamics will likely vary across space and time, due in part to spatial variation in ecosystem properties in Arctic watersheds. Here we examined watershed controls on DOM composition in 69 streams and rivers draining heterogeneous landscapes across a broad region of Arctic Alaska. We characterized DOM using bulk dissolved organic carbon (DOC) concentration, optical properties, and chemical fractionation and classified watersheds based on permafrost characteristics (mapping of parent material and ground ice content, modeling of thermal state) and ecotypes. Parent material and ground ice content significantly affected the amount and composition of DOM. DOC concentrations were higher in watersheds underlain by fine-grained loess compared to watersheds underlain by coarse-grained sand or shallow bedrock. DOC concentration was also higher in rivers draining ice-rich landscapes compared to rivers draining ice-poor landscapes. Similarly, specific ultraviolet absorbance (SUVA254, an index of DOM aromaticity) values were highest in watersheds underlain by fine-grained deposits or ice-rich permafrost. We also observed differences in hydrophobic organic acids, hydrophilic compounds, and DOM fluorescence across watersheds. Both DOC concentration and SUVA254 were negatively correlated with watershed active layer thickness, as determined by high-resolution permafrost modeling. Together, these findings highlight how spatial variations in permafrost physical and thermal properties can influence riverine DOM.

DOE Office of Scientific and Technical Information (OSTI.GOV)

Yang, Qichun; Zhang, Xuesong; Xu, Xingya

Riverine carbon cycling is an important, but insufficiently investigated component of the global carbon cycle. Analyses of environmental controls on riverine carbon cycling are critical for improved understanding of mechanisms regulating carbon processing and storage along the terrestrial-aquatic continuum. Here, we compile and analyze riverine dissolved organic carbon (DOC) concentration data from 1402 United States Geological Survey (USGS) gauge stations to examine the spatial variability and environmental controls of DOC concentrations in the United States (U.S.) surface waters. DOC concentrations exhibit high spatial variability, with an average of 6.42 ± 6.47 mg C/ L (Mean ± Standard Deviation). In general,more » high DOC concentrations occur in the Upper Mississippi River basin and the Southeastern U.S., while low concentrations are mainly distributed in the Western U.S. Single-factor analysis indicates that slope of drainage areas, wetlands, forests, percentage of first-order streams, and instream nutrients (such as nitrogen and phosphorus) pronouncedly influence DOC concentrations, but the explanatory power of each bivariate model is lower than 35%. Analyses based on the general multi-linear regression models suggest DOC concentrations are jointly impacted by multiple factors. Soil properties mainly show positive correlations with DOC concentrations; forest and shrub lands have positive correlations with DOC concentrations, but urban area and croplands demonstrate negative impacts; total instream phosphorus and dam density correlate positively with DOC concentrations. Notably, the relative importance of these environmental controls varies substantially across major U.S. water resource regions. In addition, DOC concentrations and environmental controls also show significant variability from small streams to large rivers, which may be caused by changing carbon sources and removal rates by river orders. In sum, our results reveal that general multi-linear regression analysis of twenty one terrestrial and aquatic environmental factors can partially explain (56%) the DOC concentration variation. In conclusion, this study highlights the complexity of the interactions among these environmental factors in determining DOC concentrations, thus calls for processes-based, non-linear methodologies to constrain uncertainties in riverine DOC cycling.« less

Controls on soil solution nitrogen along an altitudinal gradient in the Scottish uplands.

PubMed

Jackson-Blake, L; Helliwell, R C; Britton, A J; Gibbs, S; Coull, M C; Dawson, L

2012-08-01

Nitrogen (N) deposition continues to threaten upland ecosystems, contributing to acidification, eutrophication and biodiversity loss. We present results from a monitoring study aimed at investigating the fate of this deposited N within a pristine catchment in the Cairngorm Mountains (Scotland). Six sites were established along an elevation gradient (486-908 m) spanning the key habitats of temperate maritime uplands. Bulk deposition chemistry, soil carbon content, soil solution chemistry, soil temperature and soil moisture content were monitored over a 5 year period. Results were used to assess spatial variability in soil solution N and to investigate the factors and processes driving this variability. Highest soil solution inorganic N concentrations were found in the alpine soils at the top of the hillslope. Soil carbon stock, soil solution dissolved organic carbon (DOC) and factors representing site hydrology were the best predictors of NO(3)(-) concentration, with highest concentrations at low productivity sites with low DOC and freely-draining soils. These factors act as proxies for changing net biological uptake and soil/water contact time, and therefore support the hypothesis that spatial variations in soil solution NO(3)(-) are controlled by habitat N retention capacity. Soil percent carbon was a better predictor of soil solution inorganic N concentration than mass of soil carbon. NH(4)(+) was less affected by soil hydrology than NO(3)(-) and showed the effects of net mineralization inputs, particularly at Racomitrium heath and peaty sites. Soil solution dissolved organic N concentration was strongly related to both DOC and temperature, with a stronger temperature effect at more productive sites. Due to the spatial heterogeneity in N leaching potential, a fine-scale approach to assessing surface water vulnerability to N leaching is recommended over the broad scale, critical loads approach currently in use, particularly for sensitive areas. Copyright © 2012 Elsevier B.V. All rights reserved.

Quantifying and predicting historical and future patterns of carbon fluxes from the North American Continent to Ocean

NASA Astrophysics Data System (ADS)

Tian, H.; Zhang, B.; Xu, R.; Yang, J.; Yao, Y.; Pan, S.; Lohrenz, S. E.; Cai, W. J.; He, R.; Najjar, R. G.; Friedrichs, M. A. M.; Hofmann, E. E.

2017-12-01

Carbon export through river channels to coastal waters is a fundamental component of the global carbon cycle. Changes in the terrestrial environment, both natural (e.g., climatic change, enriched CO2 concentration, and elevated ozone concentration) and anthropogenic (e.g, deforestation, cropland expansion, and urbanization) have greatly altered carbon production, stocks, decomposition, movement and export from land to river and ocean systems. However, the magnitude and spatiotemporal patterns of lateral carbon fluxes from land to oceans and the underlying mechanisms responsible for these fluxes remain far from certain. Here we applied a process-based land model with explicit representation of carbon processes in stream and rivers (Dynamic Land Ecosystem Model: DLEM 2.0) to examine how changes in climate, land use, atmospheric CO2, and nitrogen deposition have affected the carbon fluxes from North American continent to Ocean during 1980-2015. Our simulated results indicated that terrestrial carbon export shows substantially spatial and temporal variability. Of the five sub-regions (Arctic coast, Pacific coast, Gulf of Mexico, Atlantic coast, and Great lakes), the Arctic sub-region provides the highest DOC flux, whereas the Gulf of Mexico sub-region provided the highest DIC flux. However, terrestrial carbon export to the arctic oceans showed increasing trends for both DOC and DIC, whereas DOC and DIC export to the Gulf of Mexico decreased in the recent decades. Future pattern of riverine carbon fluxes would be largely dependent on the climate change and land use scenarios.

Abundant carbon substrates drive extremely high sulfate reduction rates and methane fluxes in Prairie Pothole Wetlands.

PubMed

Dalcin Martins, Paula; Hoyt, David W; Bansal, Sheel; Mills, Christopher T; Tfaily, Malak; Tangen, Brian A; Finocchiaro, Raymond G; Johnston, Michael D; McAdams, Brandon C; Solensky, Matthew J; Smith, Garrett J; Chin, Yu-Ping; Wilkins, Michael J

2017-08-01

Inland waters are increasingly recognized as critical sites of methane emissions to the atmosphere, but the biogeochemical reactions driving such fluxes are less well understood. The Prairie Pothole Region (PPR) of North America is one of the largest wetland complexes in the world, containing millions of small, shallow wetlands. The sediment pore waters of PPR wetlands contain some of the highest concentrations of dissolved organic carbon (DOC) and sulfur species ever recorded in terrestrial aquatic environments. Using a suite of geochemical and microbiological analyses, we measured the impact of sedimentary carbon and sulfur transformations in these wetlands on methane fluxes to the atmosphere. This research represents the first study of coupled geochemistry and microbiology within the PPR and demonstrates how the conversion of abundant labile DOC pools into methane results in some of the highest fluxes of this greenhouse gas to the atmosphere ever reported. Abundant DOC and sulfate additionally supported some of the highest sulfate reduction rates ever measured in terrestrial aquatic environments, which we infer to account for a large fraction of carbon mineralization in this system. Methane accumulations in zones of active sulfate reduction may be due to either the transport of free methane gas from deeper locations or the co-occurrence of methanogenesis and sulfate reduction. If both respiratory processes are concurrent, any competitive inhibition of methanogenesis by sulfate-reducing bacteria may be lessened by the presence of large labile DOC pools that yield noncompetitive substrates such as methanol. Our results reveal some of the underlying mechanisms that make PPR wetlands biogeochemical hotspots, which ultimately leads to their critical, but poorly recognized role in regional greenhouse gas emissions. © 2017 John Wiley & Sons Ltd.

Abundant carbon substrates drive extremely high sulfate reduction rates and methane fluxes in Prairie Pothole Wetlands

DOE Office of Scientific and Technical Information (OSTI.GOV)

Dalcin Martins, Paula; Hoyt, David W.; Bansal, Sheel

Inland waters are increasingly recognized as critical sites of methane emissions to the atmosphere, but the biogeochemical reactions driving such fluxes are less well understood. The Prairie Pothole Region (PPR) of North America is one of the largest wetland complexes in the world, containing millions of small, shallow wetlands. The sediment pore waters of PPR wetlands contain some of the highest concentrations of dissolved organic carbon (DOC) and sulfur species ever recorded in terrestrial aquatic environments. Using a suite of geochemical and microbiological analyses we measured the impact of sedimentary carbon and sulfur transformations in these wetlands on methane fluxesmore » to the atmosphere. This research represents the first study of coupled geochemistry and microbiology within the PPR, and demonstrates how the conversion of abundant labile DOC pools into methane results in some of the highest fluxes of this greenhouse gas to the atmosphere ever reported. Abundant DOC and sulfate additionally supported some of the highest sulfate reduction rates ever measured in terrestrial aquatic environments, which we infer to account for a large fraction of carbon mineralization in this system. Methane accumulations in zones of active sulfate reduction may be due to either the transport of free methane gas from deeper locations, or the co-occurrence of methanogenesis and sulfate reduction. If both respiratory processes are concurrent, any competitive inhibition of methanogenesis by sulfate-reducing bacteria may be lessened by the presence of large labile DOC pools that yield non-competitive substrates such as methanol. Our results reveal some of the underlying mechanisms that make PPR wetlands biogeochemical hotspots, which ultimately leads to their critical, but poorly recognized role in regional greenhouse gas emissions.« less

Abundant carbon substrates drive extremely high sulfate reduction rates and methane fluxes in Prairie Pothole Wetlands

USGS Publications Warehouse

Martins, Paula; Hoyt, David W.; Bansal, Sheel; Mills, Christopher T.; Tfaily, Malak; Tangen, Brian; Finocchiaro, Raymond; Johnston, Michael D.; McAdams, Brandon C.; Solensky, Matthew J.; Smith, Garrett J.; Chin, Yu-Ping; Wilkins, Michael J.

2017-01-01

Inland waters are increasingly recognized as critical sites of methane emissions to the atmosphere, but the biogeochemical reactions driving such fluxes are less well understood. The Prairie Pothole Region (PPR) of North America is one of the largest wetland complexes in the world, containing millions of small, shallow wetlands. The sediment pore waters of PPR wetlands contain some of the highest concentrations of dissolved organic carbon (DOC) and sulfur species ever recorded in terrestrial aquatic environments. Using a suite of geochemical and microbiological analyses, we measured the impact of sedimentary carbon and sulfur transformations in these wetlands on methane fluxes to the atmosphere. This research represents the first study of coupled geochemistry and microbiology within the PPR and demonstrates how the conversion of abundant labile DOC pools into methane results in some of the highest fluxes of this greenhouse gas to the atmosphere ever reported. Abundant DOC and sulfate additionally supported some of the highest sulfate reduction rates ever measured in terrestrial aquatic environments, which we infer to account for a large fraction of carbon mineralization in this system. Methane accumulations in zones of active sulfate reduction may be due to either the transport of free methane gas from deeper locations or the co-occurrence of methanogenesis and sulfate reduction. If both respiratory processes are concurrent, any competitive inhibition of methanogenesis by sulfate-reducing bacteria may be lessened by the presence of large labile DOC pools that yield noncompetitive substrates such as methanol. Our results reveal some of the underlying mechanisms that make PPR wetlands biogeochemical hotspots, which ultimately leads to their critical, but poorly recognized role in regional greenhouse gas emissions.

Dissolved organic carbon fluxes from soils in the Alaskan coastal temperate rainforest

NASA Astrophysics Data System (ADS)

D'Amore, D. V.; Edwards, R.; Hood, E. W.; Herendeen, P. A.; Valentine, D.

2011-12-01

Soil saturation and temperature are the primary factors that influence soil carbon cycling. Interactions between these factors vary by soil type, climate, and landscape position, causing uncertainty in predicting soil carbon flux from. The soils of the North American perhumid coastal temperate rainforest (NCTR) store massive amounts of carbon, yet there is no estimate of dissolved organic carbon (DOC) export from different soil types in the region. There are also no working models that describe the influence of soil saturation and temperature on the export of DOC from soils. To address this key information gap, we measured soil water table elevation, soil temperature, and soil and stream DOC concentrations to calculate DOC flux across a soil hydrologic gradient that included upland soils, forested wetland soils, and sloping bog soils in the NCTR of southeast Alaska. We found that increased soil temperature and frequent fluctuations of soil water tables promoted the export of large quantities of DOC from wetland soils and relatively high amounts of DOC from mineral soils. Average area-weighted DOC flux ranged from 7.7 to 33.0 g C m-2 y-1 across a gradient of hydropedologic soil types. The total area specific export of carbon as DOC for upland, forested wetland and sloping bog catchments was 77, 306, and 329 Kg C ha-1 y-1 respectively. The annual rate of carbon export from wetland soils in this region is among the highest reported in the literature. These findings highlight the importance of terrestrial-aquatic fluxes of DOC as a pathway for carbon loss in the NCTR.

Long-term trends in dissolved iron and DOC concentration linked to nitrate depletion in riparian soils

NASA Astrophysics Data System (ADS)

Musolff, Andreas; Selle, Benny; Fleckenstein, Jan H.; Oosterwoud, Marieke R.; Tittel, Jörg

2016-04-01

The instream concentrations of dissolved organic carbon (DOC) are rising in many catchments of the northern hemisphere. Elevated concentrations of DOC, mainly in the form of colored humic components, increase efforts and costs of drinking water purification. In this study, we evaluated a long-term dataset of 110 catchments draining into German drinking water reservoirs in order to assess sources of DOC and drivers of a potential long-term change. The average DOC concentrations across the wide range of different catchments were found to be well explained by the catchment's topographic wetness index. Higher wetness indices were connected to higher average DOC concentrations, which implies that catchments with shallow topography and pronounced riparian wetlands mobilize more DOC. Overall, 37% of the investigated catchments showed a significant long-term increase in DOC concentrations, while 22% exhibited significant negative trends. Moreover, we found that increasing trends in DOC were positively correlated to trends in dissolved iron concentrations at pH≤6 due to remobilization of DOC previously sorbed to iron minerals. Both, increasing trends in DOC and dissolve iron were found to be connected to decreasing trends and low concentrations of nitrate (below ~6 mg/L). This was especially observed in forested catchments where atmospheric N-depositions were the major source for nitrate availability. In these catchments, we also found long-term increases of phosphate concentrations. Therefore, we argue that dissolved iron, DOC and phosphate were jointly released under iron-reducing conditions when nitrate as a competing electron acceptor was too low in concentrations to prevent the microbial iron reduction. In contrast, we could not explain the observed increasing trends in DOC, iron and phosphate concentrations by the long-term trends of pH, sulfate or precipitation. Altogether this study gives strong evidence that both, source and long-term increases in DOC are primarily controlled by riparian wetland soils within the catchments. Here, the achievement of a long-term reduction in nitrogen deposition may in turn lead to a more pronounced iron reduction and a subsequent release of DOC and other iron-bound substances such as phosphate.

Response of oxidative enzyme activities to nitrogen deposition affects soil concentrations of dissolved organic carbon

USGS Publications Warehouse

Waldrop, M.P.; Zak, D.R.

2006-01-01

Recent evidence suggests that atmospheric nitrate (NO3- ) deposition can alter soil carbon (C) storage by directly affecting the activity of lignin-degrading soil fungi. In a laboratory experiment, we studied the direct influence of increasing soil NO 3- concentration on microbial C cycling in three different ecosystems: black oak-white oak (BOWO), sugar maple-red oak (SMRO), and sugar maple-basswood (SMBW). These ecosystems span a broad range of litter biochemistry and recalcitrance; the BOWO ecosystem contains the highest litter lignin content, SMRO had intermediate lignin content, and SMBW leaf litter has the lowest lignin content. We hypothesized that increasing soil solution NO 3- would reduce lignolytic activity in the BOWO ecosystem, due to a high abundance of white-rot fungi and lignin-rich leaf litter. Due to the low lignin content of litter in the SMBW, we further reasoned that the NO3- repression of lignolytic activity would be less dramatic due to a lower relative abundance of white-rot basidiomycetes; the response in the SMRO ecosystem should be intermediate. We increased soil solution NO3- concentrations in a 73-day laboratory incubation and measured microbial respiration and soil solution dissolved organic carbon (DOC) and phenolics concentrations. At the end of the incubation, we measured the activity of ??-glucosidase, N-acetyl-glucosaminidase, phenol oxidase, and peroxidase, which are extracellular enzymes involved with cellulose and lignin degradation. We quantified the fungal biomass, and we also used fungal ribosomal intergenic spacer analysis (RISA) to gain insight into fungal community composition. In the BOWO ecosystem, increasing NO 3- significantly decreased oxidative enzyme activities (-30% to -54%) and increased DOC (+32% upper limit) and phenolic (+77% upper limit) concentrations. In the SMRO ecosystem, we observed a significant decrease in phenol oxidase activity (-73% lower limit) and an increase in soluble phenolic concentrations (+57% upper limit) in response to increasing NO 3- in soil solution, but there was no significant change in DOC concentration. In contrast to these patterns, increasing soil solution NO3- in the SMBW soil resulted in significantly greater phenol oxidase activity (+700% upper limit) and a trend toward lower DOC production (-52% lower limit). Nitrate concentration had no effect on microbial respiration or ??-glucosidase or N-acetyl-glucosaminidase activities. Fungal abundance and basidiomycete diversity tended to be highest in the BOWO soil and lowest in the SMBW, but neither displayed a consistent response to NO 3- additions. Taken together, our results demonstrate that oxidative enzyme production by microbial communities responds directly to NO3- deposition, controlling extracellular enzyme activity and DOC flux. The regulation of oxidative enzymes by different microbial communities in response to NO3- deposition highlights the fact that the composition and function of soil microbial communities directly control ecosystem-level responses to environmental change. ?? 2006 Springer Science+Business Media, Inc.

[Chromophoric dissolved organic matter absorption characteristics with relation to fluorescence in typical macrophyte, algae lake zones of Lake Taihu].

PubMed

Zhang, Yun-lin; Qin, Bo-qiang; Ma, Rong-hua; Zhu, Guang-wei; Zhang, Lu; Chen, Wei-min

2005-03-01

Chromophoric dissolved organic matter (CDOM) represents one of the primary light-absorbing species in natural waters and plays a critical in determining the aquatic light field. CDOM shows a featureless absorption spectrum that increases exponentially with decreasing wavelength, which limits the penetration of biologically damaging UV-B radiation (wavelength from 280 to 320 nm) in the water column, thus shielding aquatic organisms. CDOM absorption measurements and their relationship with dissolved organic carbon (DOC), and fluorescence are presented in typical macrophyte and algae lake zone of Lake Taihu based on a field investigation in April in 2004 and lab analysis. Absorption spectral of CDOM was measured from 240 to 800 nm using a Shimadzu UV-2401PC UV-Vis recording spectrophotometer. Fluorescence with an excitation wavelength of 355 nm, an emission wavelength of 450 nm is measured using a Shimadzu 5301 spectrofluorometer. Concentrations of DOC ranged from 6.3 to 17.2 mg/L with an average of 9.08 +/- 2.66 mg/L. CDOM absorption coefficients at 280 nm and 355 nm were in the range of 11.2 - 32.6 m(-1) (average 17.46m(-1) +/- 5.75 m(-1) and 2.4 - 8.3 m(-1) (average 4.17m(-1) +/- 1.47 m(-l)), respectively. The values of the DOC-specific absorption coefficient at 355 nm ranged from 0.31 to 0.64 L x (mg x m)-1. Fluorescence emission at 450 nm, excited at 355 nm, had a mean value of 1.32nm(-1) +/- 0.84 nm(-1). A significant lake zone difference is found in DOC concentration, CDOM absorption coefficient and fluorescence, but not in DOC-specific absorption coefficient and spectral slope coefficient. This regional distribution pattern is in agreement with the location of sources of yellow substance: highest concentrations close to river mouth under the influence of river inflow, lower values in East Lake Taihu. The values of algae lake zone are obvious larger than those of macrophyte lake zone. In Meiliang Bay, CDOM absorption, DOC concentration and fluorescence tend to decreasing from inside to mouth of the Bay. The results show a good correlation between CDOM absorption and DOC coefficients during 280 - 500 nm short wavelength intervals. The R-square coefficient between CDOM absorption and DOC concentration decreases with the increase of wavelength from 280 to 500 nm. The significant linear regression correlations between fluorescence, DOC concentration and absorption coefficients were found at 355 nm. The exponential slope coefficients ranged from 13.0 to 16.4 microm(-1) with a mean value 14.37microm(-1) +/- 0.73microm(-1), 17.3microm(-1) - 20.3microm(-1) with a mean value 19.17microm(-1) +/- 0.84microm(-1) and 12.0microm(-1) - 15.8microm(-1) with a mean value 13.38microm(-1) +/- 0.82microm(-1) over the 280 - 500 nm, 280 - 360 nm and 360 - 440 nm intervals.

Direct analysis of δ13C and concentration of dissolved organic carbon (DOC) in environmental samples by TOC-IRMS

NASA Astrophysics Data System (ADS)

Kirkels, Frédérique; Cerli, Chiara; Federherr, Eugen; Kalbitz, Karsten

2014-05-01

Dissolved organic carbon (DOC) plays an important role in carbon cycling in terrestrial and aquatic systems. Stable isotope analysis (delta 13C) of DOC could provide valuable insights in its origin, fluxes and environmental fate. Precise and routine analysis of delta 13C and DOC concentration are therefore highly desirable. A promising, new system has been developed for this purpose, linking a high-temperature combustion TOC analyzer trough an interface with a continuous flow isotope ratio mass spectrometer (Elementar group, Hanau, Germany). This TOC-IRMS system enables simultaneous stable isotope (bulk delta 13C) and concentration analysis of DOC, with high oxidation efficiency by high-temperature combustion for complex mixtures as natural DOC. To give delta 13C analysis by TOC-IRMS the necessary impulse for broad-scale application, we present a detailed evaluation of its analytical performance for realistic and challenging conditions inclusive low DOC concentrations and environmental samples. High precision (standard deviation, SD predominantly < 0.15 permil) and accuracy (R2 = 0.9997, i.e. comparison TOC-IRMS and conventional EA-IRMS) were achieved by TOC-IRMS for a broad diversity of DOC solutions. This precision is comparable or even slightly better than that typically reported for EA-IRMS systems, and improves previous techniques for δ13C analysis of DOC. Simultaneously, very good precision was obtained for DOC concentration measurements. Assessment of natural abundance and slightly 13C enriched DOC, a wide range of concentrations (0.2-150 mgC/L) and injection volumes (0.05-3 ml), demonstrated good analytical performance with negligible memory effects, no concentration/volume effects and a wide linearity. Low DOC concentrations (< 2 mgC/L), were correctly analyzed without any pre-concentration. Moreover, TOC-IRMS was successfully applied to analyze DOC from diverse terrestrial, freshwater and marine environments (SD < 0.23 permil). In summary, the TOC-IRMS performs fast and reliable analysis of DOC concentration and δ13C in aqueous samples, without any pre-concentration/freeze-drying. Flexible usage is highlighted by automated, online analysis, a variable injection volume, high throughput and no extensive maintenance. Sample analysis is simple, using small aliquots and with minimal sample preparation. Further investigations should focus on complex, saline matrices and very low DOC concentrations, to achieve a potential lower limit of 0.2 mgC/L. High-resolution, routine delta 13C analysis of DOC by TOC-IRMS offers opportunities for wide-scale application in terrestrial, freshwater and marine research to elucidate the role of DOC in biogeochemical processes and ecosystem functioning.

Quantifying nutrient sources in an upland catchment using multiple chemical and isotopic tracers

NASA Astrophysics Data System (ADS)

Sebestyen, S. D.; Boyer, E. W.; Shanley, J. B.; Doctor, D. H.; Kendall, C.; Aiken, G. R.

2006-12-01

To explore processes that control the temporal variation of nutrients in surface waters, we measured multiple environmental tracers at the Sleepers River Research Watershed, an upland catchment in northeastern Vermont, USA. Using a set of high-frequency stream water samples, we quantified the variation of nutrients over a range of stream flow conditions with chemical and isotopic tracers of water, nitrate, and dissolved organic carbon (DOC). Stream water concentrations of nitrogen (predominantly in the forms of nitrate and dissolved organic nitrogen) and DOC reflected mixing of water contributed from distinct sources in the forested landscape. Water isotopic signatures and end-member mixing analysis revealed when solutes entered the stream from these sources and that the sources were linked to the stream by preferential shallow subsurface and overland flow paths. Results from the tracers indicated that freshly-leached, terrestrial organic matter was the overwhelming source of high DOC concentrations in stream water. In contrast, in this region where atmospheric nitrogen deposition is chronically elevated, the highest concentrations of stream nitrate were attributable to atmospheric sources that were transported via melting snow and rain fall. These findings are consistent with a conceptual model of the landscape in which coupled hydrological and biogeochemical processes interact to control stream solute variability over time.

An Analysis of Terrestrial and Aquatic Environmental Controls of Riverine Dissolved Organic Carbon in the Conterminous United States

DOE PAGES

Yang, Qichun; Zhang, Xuesong; Xu, Xingya; ...

2017-05-29

Riverine carbon cycling is an important, but insufficiently investigated component of the global carbon cycle. Analyses of environmental controls on riverine carbon cycling are critical for improved understanding of mechanisms regulating carbon processing and storage along the terrestrial-aquatic continuum. Here, we compile and analyze riverine dissolved organic carbon (DOC) concentration data from 1402 United States Geological Survey (USGS) gauge stations to examine the spatial variability and environmental controls of DOC concentrations in the United States (U.S.) surface waters. DOC concentrations exhibit high spatial variability, with an average of 6.42 ± 6.47 mg C/ L (Mean ± Standard Deviation). In general,more » high DOC concentrations occur in the Upper Mississippi River basin and the Southeastern U.S., while low concentrations are mainly distributed in the Western U.S. Single-factor analysis indicates that slope of drainage areas, wetlands, forests, percentage of first-order streams, and instream nutrients (such as nitrogen and phosphorus) pronouncedly influence DOC concentrations, but the explanatory power of each bivariate model is lower than 35%. Analyses based on the general multi-linear regression models suggest DOC concentrations are jointly impacted by multiple factors. Soil properties mainly show positive correlations with DOC concentrations; forest and shrub lands have positive correlations with DOC concentrations, but urban area and croplands demonstrate negative impacts; total instream phosphorus and dam density correlate positively with DOC concentrations. Notably, the relative importance of these environmental controls varies substantially across major U.S. water resource regions. In addition, DOC concentrations and environmental controls also show significant variability from small streams to large rivers, which may be caused by changing carbon sources and removal rates by river orders. In sum, our results reveal that general multi-linear regression analysis of twenty one terrestrial and aquatic environmental factors can partially explain (56%) the DOC concentration variation. In conclusion, this study highlights the complexity of the interactions among these environmental factors in determining DOC concentrations, thus calls for processes-based, non-linear methodologies to constrain uncertainties in riverine DOC cycling.« less

Spatial pattern of dissolved organic matter (DOM) along a stream drainage in a forested, Piedmont catchment

NASA Astrophysics Data System (ADS)

Inamdar, S. P.; Singh, S.

2013-12-01

Understanding how dissolved organic matter (DOM) varies spatially in catchments and the processes and mechanisms that regulate this variation is critical for developing accurate and reliable models of DOM. We determined the concentrations and composition of DOM at multiple locations along a stream drainage network in a 79 ha forested, Piedmont, watershed in Maryland, USA. DOM concentrations and composition was compared for five stream locations during baseflow (drainage areas - 0.62, 3.5, 4.5, 12 and 79 ha) and three locations (3.5, 12, 79 ha) for storm flow. Sampling was conducted by manual grab samples and automated ISCO samplers. DOM composition was characterized using a suite of spectrofluorometric indices which included - HIX, a254, and FI. A site-specific PARAFAC model was also developed for DOM fluorescence to determine the humic-, fulvic-, and protein-like DOM constituents. Hydrologic flow paths during baseflow and stormflow were characterized for all stream locations using an end-member mixing model (EMMA). DOM varied notably across the sampled positions for baseflow and stormflow. During baseflow, mean DOC concentrations for the sampled locations ranged between 0.99-3.1 mg/L whereas for stormflow the range was 5.22-8.11 mg/L. Not surprisingly, DOM was more humic and aromatic during stormflow versus baseflow. The 3.5 ha stream drainage location that contained a large wetland yielded the highest DOC concentration as well as the most humic and aromatic DOM, during both, baseflow and stormflow. In contrast, a headwater stream location (0.62 ha) that received runoff from a groundwater seep registered the highest mean value for % protein-like DOM (30%) and the lowest index for aromaticity (mean a254 = 6.52) during baseflow. During stormflow, the mean % protein-like DOM was highest at the largest 79 ha drainage location (mean = 11.8%) and this site also registered the lowest mean value for a254 (46.3). Stream drainage locations that received a larger proportion of runoff along surficial flow paths produced a more aromatic and humic DOM with high DOC concentrations; whereas those with a greater proportion of groundwater contributions produced DOM with greater % of protein-like content. Overall, our observations suggest that occurrence of wetlands and the nature of hydrologic flow paths were the key determinants for the spatial pattern of DOM.

Changes in the character of DOC in streams during storms in two Midwestern watersheds with contrasting land uses

USGS Publications Warehouse

Vidon, P.; Wagner, L.E.; Soyeux, E.

2008-01-01

Dissolved organic carbon (DOC) dynamics in streams is important, yet few studies focus on DOC dynamics in Midwestern streams during storms. In this study, stream DOC dynamics during storms in two Midwestern watersheds with contrasting land uses, the change in character of stream DOC during storms, and the usability of DOC as a hydrologic tracer in artificially drained landscapes of the Midwest are investigated. Major cation/DOC concentrations, and DOC specific UV absorbance (SUVA) and fluorescence index (FI) were monitored at 2-4 h intervals during three spring storms. Although DOC is less aromatic in the mixed land use watershed than in the agricultural watershed, land use has little impact on stream DOC concentration during storms. For both watersheds, DOC concentration follows discharge, and SUVA and FI values indicate an increase in stream DOC aromaticity and lignin content during storms. The comparison of DOC/major cation flushing dynamics indicates that DOC is mainly exported via overland flow/macropore flow. In both watersheds, the increase in DOC concentration in the streams during storms corresponds to a shift in the source of DOC from DOC originating from mineral soil layers of the soil profile at baseflow, to DOC originating from surficial soil layers richer in aromatic substances and lignin during storms. Results also suggest that DOC, SUVA and FI could be used as hydrologic tracers in artificially drained landscapes of the Midwest. These results underscore the importance of sampling streams for DOC during high flow periods in order to understand the fate of DOC in streams. ?? 2008 Springer Science+Business Media B.V.

Impact of catchment geophysical characteristics and climate on the regional variability of dissolved organic carbon (DOC) in surface water.

PubMed

Cool, Geneviève; Lebel, Alexandre; Sadiq, Rehan; Rodriguez, Manuel J

2014-08-15

Dissolved organic carbon (DOC) is a recognized indicator of natural organic matter (NOM) in surface waters. The aim of this paper is twofold: to evaluate the impact of geophysical characteristics, climate and ecological zones on DOC concentrations in surface waters and, to develop a statistical model to estimate the regional variability of these concentrations. In this study, multilevel statistical analysis was used to achieve three specific objectives: (1) evaluate the influence of climate and geophysical characteristics on DOC concentrations in surface waters; (2) compare the influence of geophysical characteristics and ecological zones on DOC concentrations in surface waters; and (3) develop a model to estimate the most accurate DOC concentrations in surface waters. The case study involved 115 catchments from surface waters in the Province of Quebec, Canada. Results showed that mean temperatures recorded 60 days prior to sampling, total precipitation 10 days prior to sampling and percentages of wetlands, coniferous forests and mixed forests have a significant positive influence on DOC concentrations in surface waters. The catchment mean slope had a significant negative influence on DOC concentrations in surface waters. Water type (lake or river) and deciduous forest variables were not significant. The ecological zones had a significant influence on DOC concentrations. However, geophysical characteristics (wetlands, forests and slope) estimated DOC concentrations more accurately. A model describing the variability of DOC concentrations was developed and can be used, in future research, for estimating DBPs in drinking water as well evaluating the impact of climate change on the quality of surface waters and drinking water. Copyright © 2014 Elsevier B.V. All rights reserved.

Seasonal changes in concentrations of dissolved pesticides and organic carbon in the Sacramento-San Joaquin delta, California, 1994-1996

USGS Publications Warehouse

Orlando, James L.; Kuivila, Kathryn

2006-01-01

The Sacramento-San Joaquin Delta (Delta) of California is an ecologically rich and hydrologically complex region that receives runoff from nearly one-quarter of the state. Water-quality studies of surface water in the region have found dissolved pesticides in winter storm runoff at concentrations toxic to some aquatic invertebrates. However, scientists have little information on pesticide concentrations in the Delta on a seasonal timescale or the importance of pesticide contributions from within-Delta sources. Consequently, the U.S. Geological Survey conducted a study from 1994 to 1996 during which water samples were collected seasonally from 31 sites located within the Delta and on major tributaries to the Delta. Water samples were analyzed for 20 current-use pesticides and dissolved organic carbon. During the study, 11 current-use pesticides were detected; maximum concentrations ranging from 17 ng/L (for trifluralin) to 1,160 ng/L (for metolachlor). The highest concentrations of five pesticides (carbaryl, carbofuran, metolachlor, molinate, and simazine) were greater than 900 ng/L. The greatest number of pesticides was detected in the summer of 1994, whereas the least number were detected in the winter of 1994. The herbicides metolachlor and simazine were the most frequently detected pesticides and were detected in five of the six sampling seasons. The herbicides molinate and EPTC were detected only during the three summer sampling seasons. A comparison of pesticides detected during the spring and summer of 1995 showed some seasonal variability. Comparison of the three summer seasons sampled showed that a larger number of pesticides were detected, and with generally higher maximum concentrations, in 1994 than in 1995 or 1996. Dissolved organic carbon (DOC) concentrations ranged, over the course of the study, from 1.4 mg/L to 10.4 mg/L, and had a median concentration of 3.8 mg/L. On a seasonal basis, the lowest maximum DOC concentrations occurred during the summer and winter of 1994. The highest median DOC concentration on a seasonal basis occurred in the spring of 1995. This previously unreported data is being published now to provide historical information on pesticide concentrations in the Delta to water managers and the scientific community.

DOC and DON Dynamics along the Bagmati Drainage Network in Kathmandu Valley

NASA Astrophysics Data System (ADS)

Bhatt, M. P.; McDowell, W. H.

2005-05-01

We studied organic matter dynamics and inorganic chemistry of the Bagmati River in Kathmandu valley, Nepal, to understand the influence of human and geochemical processes on chemical loads along the drainage system. Population density appears to be the most fundamental control on the chemistry of surface waters within the Bagmati drainage system. DOC concentration increases 10-fold with distance downstream (from 2.38 to 23.95 mg/L) and shows a strong relationship with human population density. The composition of river water (nutrients, Cl) suggests that sewage effluent to the river has a major effect on water quality. Concentrations were highest during summer, and lowest during the winter monsoon season. In contrast to DOC, DON concentration shows surprisingly little variation, and tends to decrease in concentration with distance downstream. Ammonium contributes almost all nitrogen in the total dissolved nitrogen fraction and the concentration of nitrate is negligible, probably due to rapid denitrification within the stream channel under relatively low-oxygen conditions. Decreases in sulfate along the stream channel may also be due to the reduction of sulfate to sulfide due to the heavy organic matter loading. Water quality is unacceptable for any use and the whole ecosystem is severely affected within the urban areas. Based on a comparison of downstream and upstream water quality, it appears that human activities along the Bagmati, principally inputs of human sewage, are largely responsible for the changes in surface water chemistry within Kathmandu valley.

Dissolved organic carbon in runoff and tile-drain water under corn and forage fertilized with hog manure.

PubMed

Royer, Isabelle; Angers, Denis A; Chantigny, Martin H; Simard, Régis R; Cluis, Daniel

2007-01-01

Dissolved organic carbon (DOC) export from soils can play a significant role in soil C cycling and in nutrient and pollutant transport. However, information about DOC losses from agricultural soils as influenced by management practices is scarce. We compared the effects of mineral fertilizer (MF) and liquid hog manure (LHM) applications on the concentration and molecular size of DOC released in runoff and tile-drain water under corn (Zea mays L.) and forage cropping systems. Runoff and tile-drain water samples were collected during a 2-mo period (October to December 1998) and DOC concentration was measured. Characterization of DOC was performed by tangential ultrafiltration with nominal cut-offs at 3 and 100 kDa. Mean concentration of DOC in runoff water (12.7 mg DOC L(-1)) was higher than in tile-drain water (6.5 mg DOC L(-1)). Incorporation of corn residues increased the DOC concentration by 6- to 17-fold in surface runoff, but this effect was short-lived. In runoff water, the relative size of the DOC molecules increased when corn residues and LHM were applied probably due to partial microbial breakdown of these organic materials and to a faster decomposition or preferential adsorption of the small molecules. The DOC concentration in tile-drain water was slightly higher under forage (7.5 mg DOC L(-1)) than under corn (5.4 mg DOC L(-1)) even though the application rates of LHM were higher in corn plots. We suggest that preferential flow facilitated the migration of DOC to tile drains in forage plots. In conclusion, incorporation of corn residues and LHM increased the concentration of DOC and the relative size of the molecules in surface runoff water, whereas DOC in tile-drain water was mostly influenced by the cropping system with relatively more DOC and larger molecules under forage than corn.

Intrinsic Controls of Groundwater-Surface Water Dissolved Organic Carbon Quality and Quantity on Hyporheic Carbon Oxidation.

NASA Astrophysics Data System (ADS)

Garayburu-Caruso, V. A.; Stegen, J.; Graham, E.

2017-12-01

Inputs of dissolved organic carbon (DOC) and nutrients from groundwater (GW) and surface water (SW) to the hyporheic zone strongly influence biogeochemical processes. Despite increased research efforts, we still lack a mechanistic understanding of the conditions driving elevated hyporheic metabolism. This work explores hyporheic carbon oxidation from a thermodynamic perspective by evaluating changes in metabolic rates within hyporheic zone sediments in response to changes on DOC concentration and thermodynamic profiles that are characteristic of GW and SW sources. We hypothesize that GW DOC is protected from microbial oxidation due to low concentration and that SW DOC is protected due low thermodynamic favorability. Further, we propose that GW-SW mixing can simultaneously overcome both limitations and stimulate carbon oxidation. Hyporheic sediments from the Hanford site in Richland, WA were exposed to ambient, 2-,5- and 10-fold concentrations of natural DOC from SW and GW sources, separately, and incubated at in-situ temperature. The two DOC sources supply contrasting thermodynamic profiles, with GW providing lower concentration but more thermodynamically favorable DOC and SW higher concentration, more recalcitrant DOC. Across DOC treatments we characterized time series of oxygen concentration, DOC concentration, and pH as well as endpoint measurements of DOC thermodynamics using Fourier transform ion cyclotron resonance mass spectrometry (FT-ICR-MS). Our results suggest that hyporheic metabolism of distinct carbon pools (GW or SW) can be limited by concentration or thermodynamic favorability. Our work provides an experimental approach to contribute to mechanistic understanding of freshwater carbon oxidation, and a process-based foundation for the development of watershed-scale hydrobiogeochemical models.

Potential changes in bacterial metabolism associated with increased water temperature and nutrient inputs in tropical humic lagoons.

PubMed

Scofield, Vinicius; Jacques, Saulo M S; Guimarães, Jean R D; Farjalla, Vinicius F

2015-01-01

Temperature and nutrient concentrations regulate aquatic bacterial metabolism. However, few studies have focused on the effect of the interaction between these factors on bacterial processes, and none have been performed in tropical aquatic ecosystems. We analyzed the main and interactive effects of changes in water temperature and N and P concentrations on bacterioplankton production (BP), bacterioplankton respiration (BR) and bacterial growth efficiency (BGE) in tropical coastal lagoons. We used a factorial design with three levels of water temperature (25, 30, and 35°C) and four levels of N and/or P additions (Control, N, P, and NP additions) in five tropical humic lagoons. When data for all lagoons were pooled together, a weak interaction was observed between the increase in water temperature and the addition of nutrients. Water temperature alone had the greatest impact on bacterial metabolism by increasing BR, decreasing BP, and decreasing BGE. An increase of 1°C lead to an increase of ~4% in BR, a decrease of ~0.9% in BP, and a decrease of ~4% in BGE. When data were analyzed separately, lagoons responded differently to nutrient additions depending on Dissolved Organic Carbon (DOC) concentration. Lagoons with lowest DOC concentrations showed the strongest responses to nutrient additions: BP increased in response to N, P, and their interaction, BR increased in response to N and the interaction between N and P, and BGE was negatively affected, mainly by the interaction between N and P additions. Lagoons with the highest DOC concentrations showed almost no significant relationship with nutrient additions. Taken together, these results show that different environmental drivers impact bacterial processes at different scales. Changes of bacterial metabolism related to the increase of water temperature are consistent between lagoons, therefore their consequences can be predicted at a regional scale, while the effect of nutrient inputs is specific to different lagoons but seems to be related to the DOC concentration.

Potential changes in bacterial metabolism associated with increased water temperature and nutrient inputs in tropical humic lagoons

PubMed Central

Scofield, Vinicius; Jacques, Saulo M. S.; Guimarães, Jean R. D.; Farjalla, Vinicius F.

2015-01-01

Temperature and nutrient concentrations regulate aquatic bacterial metabolism. However, few studies have focused on the effect of the interaction between these factors on bacterial processes, and none have been performed in tropical aquatic ecosystems. We analyzed the main and interactive effects of changes in water temperature and N and P concentrations on bacterioplankton production (BP), bacterioplankton respiration (BR) and bacterial growth efficiency (BGE) in tropical coastal lagoons. We used a factorial design with three levels of water temperature (25, 30, and 35°C) and four levels of N and/or P additions (Control, N, P, and NP additions) in five tropical humic lagoons. When data for all lagoons were pooled together, a weak interaction was observed between the increase in water temperature and the addition of nutrients. Water temperature alone had the greatest impact on bacterial metabolism by increasing BR, decreasing BP, and decreasing BGE. An increase of 1°C lead to an increase of ~4% in BR, a decrease of ~0.9% in BP, and a decrease of ~4% in BGE. When data were analyzed separately, lagoons responded differently to nutrient additions depending on Dissolved Organic Carbon (DOC) concentration. Lagoons with lowest DOC concentrations showed the strongest responses to nutrient additions: BP increased in response to N, P, and their interaction, BR increased in response to N and the interaction between N and P, and BGE was negatively affected, mainly by the interaction between N and P additions. Lagoons with the highest DOC concentrations showed almost no significant relationship with nutrient additions. Taken together, these results show that different environmental drivers impact bacterial processes at different scales. Changes of bacterial metabolism related to the increase of water temperature are consistent between lagoons, therefore their consequences can be predicted at a regional scale, while the effect of nutrient inputs is specific to different lagoons but seems to be related to the DOC concentration. PMID:25926827

Factors Controlling Methane in Arctic Lakes of Southwest Greenland.

PubMed

Northington, Robert M; Saros, Jasmine E

2016-01-01

We surveyed 15 lakes during the growing season of 2014 in Arctic lakes of southwest Greenland to determine which factors influence methane concentrations in these systems. Methane averaged 2.5 μmol L-1 in lakes, but varied a great deal across the landscape with lakes on older landscapes farther from the ice sheet margin having some of the highest values of methane reported in lakes in the northern hemisphere (125 μmol L-1). The most important factors influencing methane in Greenland lakes included ionic composition (SO4, Na, Cl) and chlorophyll a in the water column. DOC concentrations were also related to methane, but the short length of the study likely underestimated the influence and timing of DOC on methane concentrations in the region. Atmospheric methane concentrations are increasing globally, with freshwater ecosystems in northern latitudes continuing to serve as potentially large sources in the future. Much less is known about how freshwater lakes in Greenland fit in the global methane budget compared to other, more well-studied areas of the Arctic, hence our work provides essential data for a more complete view of this rapidly changing region.

A 5 Year Study of Carbon Fluxes from a Restored English Blanket Bog

NASA Astrophysics Data System (ADS)

Worrall, F.; Dixon, S.; Evans, M.

2014-12-01

This study aimed to measure the effects of ecological restoration on blanket peat water table depths, DOC concentrations and CO2 fluxes. In April 2003 the Bleaklow Plateau, an extensive area of deep blanket peat in the Peak District National Park, northern England, was devegetated by a wildfire. As a result the area was selected for large scale restoration. In this study we considered a 5-year study of four restored sites in comparison to both an unrestored, bare peat control and to vegetated control that did not require restoration. Results suggested that sites with revegetation alongside slope stabilisation had the highest rates of photosynthesis and were the largest net (daylight hours) sinks of CO2. Bare sites were the largest net sources of CO2 and had the deepest water table depths. Sites with gully wall stabilisation were between 5-8 times more likely to be net CO2 sinks than the bare sites. Revegetation without gully flow blocking using plastic dams did not have a large effect on water table depths in and around the gullies investigated whereas a blocked gully had water table depths comparable to a naturally revegetating gully. A ten centimetre lowering in water table depth decreased the probability of observing a net CO2 sink, on a given site, by up to 30%. With respect to DOC the study showed that the average soil porewater DOC concentration on the restored sites rose significantly over the 5 year study representing a 34% increase relative to the vegetated control and an 11% increase relative to the unrestored, bare control. Soil pore water concentrations were not significantly different from surface runoff DOC concentrations and therefore restoration as conducted by this study would have contributed to water quality deterioration in the catchment. The most important conclusion of this research was that restoration interventions were apparently effective at increasing the likelihood of net CO2 sink behaviour and raising water tables on degraded, climatically marginal blanket bog. However, had water table restoration been conducted alongside revegetation then a significant decline in DOC concentrations could have also been realised.

Concentration, UV-spectroscopic characteristics and fractionation of DOC in stormflow from an urban stream, Southern California, USA

USGS Publications Warehouse

Izbicki, J.A.; Pimentel, I.M.; Johnson, Russell; Aiken, G.R.; Leenheer, J.

2007-01-01

The composition of dissolved organic carbon (DOC) in stormflow from urban areas has been greatly altered, both directly and indirectly, by human activities and there is concern that there may be public health issues associated with DOC, which has unknown composition from different sources within urban watersheds. This study evaluated changes in the concentration and composition of DOC in stormflow in the Santa Ana River and its tributaries between 1995 and 2004 using a simplified approach based on the differences in the optical properties of DOC and using operationally defined differences in molecular weight and solubility. The data show changes in the composition of DOC in stormflow during the rainy season and differences associated with runoff from different parts of the basin, including extensive upland areas burned prior to the 2004 rainy season.Samples were collected from the Santa Ana River, which drains ~6950 km2 of the densely populated coastal area of southern California, during 23 stormflows between 1995 and 2004. Dissolved organic carbon (DOC) concentrations during the first stormflows of the ‘winter’ (November to March) rainy season increased rapidly with streamflow and were positively correlated with increased faecal indicator bacteria concentrations. DOC concentrations were not correlated with streamflow or with other constituents during stormflows later in the rainy season and DOC had increasing UV absorbance per unit carbon as the rainy season progressed. DOC concentrations in stormflow from an urban drain tributary to the river also increased during stormflow and were greater than concentrations in the river. DOC concentrations in stormflow from a tributary stream, draining urban and agricultural land that contained more than 320 000 animals, mostly dairy cows, were higher than concentrations in stormflow from the river and from the urban drain. Fires that burned large areas of the basin before the 2004 rainy season did not increase DOC concentrations in the river during stormflow after the fires – possibly because the large watershed of the river damped the effect of the fires. However, the fires increased the hydrophobic neutral organic carbon fraction of DOC in stormflow from the urban drain and the tributary stream.

Microbial and Dissolved Organic Carbon Characterization of Stormflow in the Santa Ana River at Imperial Highway, Southern California, 1999-2002

USGS Publications Warehouse

Izbicki, John A.; Pimentel, M. Isabel; Leddy, Menu; Bergamaschi, Brian A.

2004-01-01

The Santa Ana River drains about 2,670 square miles of densely populated coastal southern California, near Los Angeles. Almost all the flow in the river, more than 200,000 acre-feet annually, is diverted to ponds where it infiltrates and recharges underlying aquifers pumped to supply water for more than 2 million people. Base flow in the river is almost entirely treated municipal wastewater discharged from upstream treatment plants and, in the past, stormflow was considered a source of high-quality water suitable for use as a source of ground-water recharge that would dilute poorer quality water recharged during base flow. Stormflow in the Santa Ana River at the Imperial Highway diversion contains total coliform bacteria concentrations as high as 3,400,000 colonies per 100 mL (milliliters). Fecal indicator bacteria concentrations, including fecal coliforms, Escherichia coli, and enterococci, were as high as 310,000, 84,000, and 102,000 colonies per 100 mL, respectively. Although concentrations were high owing to urban runoff during the first stormflow of the rainy season, the highest concentrations occurred during the recessional flows of the first stormflow of the rainy season after streamflow returned to pre-storm conditions. Molecular indicators of microbiological organisms in stormflow, including phospholipid fatty acid (PLFA) and genetic data, show that the diversity of the total microbial population decreases during stormflow while fecal indicator bacteria concentrations increase. This suggests that the source of the bacteria must be poorly diverse and dominated by only a few types of bacteria. Although direct runoff of fecal indicator bacteria from urban areas occurs, this process cannot explain the very high concentrations of fecal indicator bacteria in runoff from upstream parts of the basin characterized by urban, agricultural (including more than 300,000 head of dairy cattle), and other land uses. Although other explanations are possible, fecal indicator bacteria concentrations and molecular microbiological data indicate accumulation and extended survival of bacteria in streambed sediments, and subsequent mobilization of those sediments and associated bacteria during stormflow. Both PLFA and genetic data indicate that water from dairy-waste storage ponds was not present during sampled stormflows. This is consistent with the relatively dry conditions and the absence of large stormflows during the study. Dissolved organic carbon (DOC) concentrations in stormflow ranged from 3 to 15.3 mg/L. In general, concentrations increased during stormflow and were distributed across the stormflow hydrograph in a manner similar to that of fecal indicator bacteria. DOC concentrations typically remained high for several days after flow returned to pre-storm conditions. Ultraviolet absorbance, excitation emission spectroscopy, and sequential fractionation of DOC using XAD-8 and XAD-4 resins showed that the composition of DOC changed rapidly during stormflow. Hydrophobic and hydrophilic acids were the largest fraction of DOC composing between 27 and 45 percent and between 24 and 37 percent of the DOC, respectively. The fraction of DOC composed of hydrophobic acids decreased due to urban runoff and increased during the recession of the first stormflow of the rainy season; the hydrophilic-acid fraction generally decreased throughout the stormflow hydrograph; the transhydrophilic-acid fraction did not vary greatly during stormflow; and the hydrophobic-neutral fraction increased from low values in base flow to almost 30 percent of the DOC after more soluble and more mobile hydrophobic and hydrophilic acids were washed from urban areas. Comparison of ultraviolet absorbance data with data collected during previous studies shows that the optical properties and, presumably, the composition of the DOC were different in this study than DOC collected during wetter periods. Samples of shallow ground water collec

Nutrient dynamics across a dissolved organic carbon and burn gradient in central Siberia

NASA Astrophysics Data System (ADS)

Rodriguez-Cardona, B.; Coble, A. A.; Prokishkin, A. S.; Kolosov, R.; Spencer, R. G.; Wymore, A.; McDowell, W. H.

2016-12-01

In stream ecosystems, dissolved organic carbon (DOC) and nitrogen (N) processing are tightly linked. In temperate streams, greater DOC concentrations and higher DOC:NO3- ratios promote the greatest nitrate (NO3-) uptake. However, less is known about this relationship in other biomes including the arctic which is undergoing changes due to climate change contributing to thawing of permafrost and alterations in biogeochemical cycles in soils and streams. Headwater streams draining into the N. Tunguska River in the central Siberian plateau are affected by forest fires but little is known about the aquatic biogeochemical implications in both a thawing and burning landscape. There are clear patterns between carbon concentration and fire history where generally DOC concentration in streams decrease after fires and older burn sites have shown greater DOC concentrations and more bioavailable DOC that could promote greater heterotrophic uptake of NO3-. However, the relationship between nutrient dynamics, organic matter composition, and fire history in streams is not very clear. In order to assess the influence of organic matter composition and DOC concentration on nutrient uptake in arctic streams, we conducted a series of short-term nutrient addition experiments following the tracer addition for spiraling curve characterization (TASCC) method, consisting of NO3- and NH4++PO43- additions, across 4 streams that comprise a fire gradient that spans 3- >100 years since the last burn with DOC concentrations ranging between 12-23 mg C/L. We hypothesized that nutrient uptake would be greatest in older burn sites due to greater DOC concentrations and availability. We will specifically examine how nutrient uptake relates to DOC concentration and OM composition (analyzed via FTICR-MS) across the burn gradient. Across the four sites DOC concentration and DOC:NO3- ratios decreased from old burn sites to recently burned sites. Results presented here can elucidate on the potential impacts of permafrost thawing and forest fires on nutrient dynamics in arctic streams.

CDOM fluorescence as a proxy of DOC concentration in natural waters: a comparison of four contrasting tropical systems.

PubMed

Rochelle-Newall, E; Hulot, F D; Janeau, J L; Merroune, A

2014-01-01

Chromophoric dissolved organic matter (CDOM) fluorescence or absorption is often proposed as a rapid alternative to chemical methods for the estimation of bulk dissolved organic carbon (DOC) concentration in natural waters. However, the robustness of this method across a wide range of systems remains to be shown. We measured CDOM fluorescence and DOC concentration in four tropical freshwater and coastal environments (estuary and coastal, tropical shallow lakes, water from the freshwater lens of two small islands, and soil leachates). We found that although this method can provide an estimation of DOC concentration in sites with low variability in DOC and CDOM sources in systems where the variability of DOC and CDOM sources are high, this method should not be used as it will lead to errors in the estimation of the bulk DOC concentration.

Geomorphic Influences on Large Wood Dam Loadings, Particulate Organic Matter and Dissolved Organic Carbon in an 0ld-Growth Northern Hardwood Watershed

Treesearch

P. Charles Goebel; Kurt S. Pregitzer; Brain J. Palik

2003-01-01

We quantified large wood loadings and seasonal concentrations of particulate organic matter (POM) and dissolved organic carbon (DOC) in three different geomonghic zones (each with unique hydrogeomorphic characteristics) of a pristine, old-growth northern hardwood watershed. The highest large wood dam loadings were in the high-gradient, bedrock controlled geomorphic...

[Effects of forest regeneration patterns on the quantity and chemical structure of soil solution dissolved organic matter in a subtropical forest.

PubMed

Yuan, Xiao Chun; Lin, Wei Sheng; Pu, Xiao Ting; Yang, Zhi Rong; Zheng, Wei; Chen, Yue Min; Yang, Yu Sheng

2016-06-01

Using the negative pressure sampling method, the concentrations and spectral characte-ristics of dissolved organic matter (DOM) of soil solution were studied at 0-15, 15-30, 30-60 cm layers in Castanopsis carlesii forest (BF), human-assisted naturally regenerated C. carlesii forest (RF), C. carlesii plantation (CP) in evergreen broad-leaved forests in Sanming City, Fujian Pro-vince. The results showed that the overall trend of dissolved organic carbon (DOC) concentrations in soil solution was RF>CP>BF, and the concentration of dissolved organic nitrogen (DON) was highest in C. carlesii plantation. The concentrations of DOC and DON in surface soil (0-15 cm) were all significantly higher than in the subsurface (30-60 cm). The aromatic index (AI) was in the order of RF>CP>BF, and as a whole, the highest AI was observed in the surface soil. Higher fluorescence intensity and a short wave absorption peak (320 nm) were observed in C. carlesii plantation, suggesting the surface soil of C. carlesii plantation was rich in decomposed substance content, while the degree of humification was lower. A medium wave absorption peak (380 nm) was observed in human-assisted naturally regenerated C. carlesii forest, indicating the degree of humification was higher which would contribute to the storage of soil fertility. In addition, DOM characte-ristics in 30-60 cm soil solution were almost unaffected by forest regeneration patterns.

Organic matter dynamics in a karstic watershed: Example from Santa Fe River, Florida, USA

NASA Astrophysics Data System (ADS)

Jin, J.; Khadka, M. B.; Martin, J. B.; Zimmerman, A. R.

2011-12-01

Organic matter (OM) dynamics in karstic watersheds can involve a range of interactions between organic and inorganic phases of carbon. These interactions include OM remineralization, which will changes its lability, increase dissolved inorganic carbon (DIC) concentrations, reduce pH, and enhance carbonate mineral dissolution. Dissolved organic carbon (DOC) concentrations are elevated in black-water rivers of northern Florida from both allochthonous and autochthonous sources and these rivers flow into and interact with the karstic Floridan Aquifer. One such river, the Santa Fe River, is split into upper confined and lower unconfined watersheds by the Cody Scarp, which represent the erosional edge of a regional confining unit. Water samples were collected from 8 sites across the entire Santa Fe River watershed (SFRW) during 9 sampling trips from December 2009 to May 2011 at flow conditions that ranged from 27 to 39 m3/s, with the highest flow about 45% higher than baseflow. At sites above the Cody Scarp, the river has elevated DOC concentrations, which decrease downstream, while dissolved inorganic carbon (DIC) and δ13C-DIC show opposite trends. At high flow, DOC concentrations progressively decrease downstream from dilution by low-DOC water discharging from the Floridan Aquifer. At low flow, the water chemistry varies little from upstream to downstream, largely because the composition of upstream water becomes similar to that of downstream water. DOC is inversely and linearly correlated with DIC and δ13C-DIC, but the slope of the correlations vary with discharge, with low flow having more negative slopes than high flow. The OM becomes more labile with distance downstream as assessed using two fluorescence indices, biological/autochthonous index (BIX) and humification index (HIX). This increase in lability suggests that DOC is produced in the river, and this production is reflected in a downstream increase in DOC flux regardless of dilution by the influx of low-DOC groundwater. Primary production was 5 to 25 times higher during high and low flow, respectively, in the lower than in the upper SFRW. No decrease in DOC with a concomitant increase in DIC was observed, however, suggesting observations of microbial consumption of OM is masked by primary production and gain of DIC-rich and DOC-poor groundwater. The upper SFRW has lower saturation index (SI; -2.9 and -0.7 for high and low flow, respectively) than the lower SFRW (0.0 and 0.3 for high and low flow, respectively). The downstream shift in SI reflects dissolution of the carbonate minerals and gain of water from the Floridan Aquifer that had equilibrated with carbonate minerals. OM dynamics in the SFRW are closely linked to the allochthonous OM derived from the upper SFRW, as well as primary production in the lower watershed. Both allochthonous and autochthonous OM can be important in abiotic processes such as carbonate mineral dissolution, but flow conditions mediate the magnitudes of the reactions.

Seasonal variations in production and consumption rates of dissolved organic carbon in an organic-rich coastal sediment

NASA Astrophysics Data System (ADS)

Alperin, M. J.; Albert, D. B.; Martens, C. S.

1994-11-01

Dissolved organic carbon (DOC) concentrations in anoxic marine sediments are controlled by at least three processes: (1) production of nonvolatile dissolved compounds, such as peptides and amino acids, soluble saccharides and fatty acids, via hydrolysis of particulate organic carbon (POC). (2) conversion of these compounds to volatile fatty acids and alcohols by fermentative bacteria. (3) consumption of volatile fatty acids and alcohols by terminal bacteria, such as sulfate reducers and methanogens. We monitored seasonal changes in concentration profiles of total DOC, nonacid-volatile (NAV) DOC and acid-volatile (AV) DOC in anoxic sediment from Cape Lookout Bight, North Carolina, USA, in order to investigate the factors that control seasonal variations in rates of hydrolysis, fermentation, and terminal metabolism. During the winter months, DOC concentrations increased continuously from 0.2 mM in the bottomwater to ~4 mM at a depth of 36 cm in the sediment column. During the summer, a large DOC maximum developed between 5 and 20 cm, with peak concentrations approaching 10 mM. The mid-depth summertime maximum was driven by increases in both NAV- and AV-DOC concentrations. Net NAV-DOC reaction rates were estimated by a diagenetic model applied to NAV-DOC concentration profiles. Depth-integrated production rates of NAV-DOC increased from February through July, suggesting that net rates of POC hydrolysis during this period are controlled by temperature. Net consumption of NAV-DOC during the late summer and early fall suggests reduced gross NAV-DOC production rates, presumably due to a decline in the availability of labile POC. A distinct subsurface peak in AV-DOC concentration developed during the late spring, when the sulfate depletion depth shoaled from 25 to 10 cm. We hypothesize that the AV-DOC maximum results from a decline in consumption by sulfate-reducing bacteria (due to sulfate limitation) and a lag in the development of an active population of methanogenic bacteria. A diagenetic model that incorporates a lag period in the sulfate reducer-methanogen transition successfully simulates the timing, magnitude, depth and shape of the AV-DOC peak.

Sources, transformations, and hydrological processes that control stream nitrate and dissolved organic matter concentrations during snowmelt in an upland forest

USGS Publications Warehouse

Sebestyen, Stephen D.; Boyer, Elizabeth W.; Shanley, James B.; Kendall, Carol; Doctor, Daniel H.; Aiken, George R.; Ohte, Nobuhito

2008-01-01

We explored catchment processes that control stream nutrient concentrations at an upland forest in northeastern Vermont, USA, where inputs of nitrogen via atmospheric deposition are among the highest in the nation and affect ecosystem functioning. We traced sources of water, nitrate, and dissolved organic matter (DOM) using stream water samples collected at high frequency during spring snowmelt. Hydrochemistry, isotopic tracers, and end‐member mixing analyses suggested the timing, sources, and source areas from which water and nutrients entered the stream. Although stream‐dissolved organic carbon (DOC) and dissolved organic nitrogen (DON) both originated from leaching of soluble organic matter, flushing responses between these two DOM components varied because of dynamic shifts of hydrological flow paths and sources that supply the highest concentrations of DOC and DON. High concentrations of stream water nitrate originated from atmospheric sources as well as nitrified sources from catchment soils. We detected nitrification in surficial soils during late snowmelt which affected the nitrate supply that was available to be transported to streams. However, isotopic tracers showed that the majority of nitrate in upslope surficial soil waters after the onset of snowmelt originated from atmospheric sources. A fraction of the atmospheric nitrogen was directly delivered to the stream, and this finding highlights the importance of quick flow pathways during snowmelt events. These findings indicate that interactions among sources, transformations, and hydrologic transport processes must be deciphered to understand why concentrations vary over time and over space as well as to elucidate the direct effects of human activities on nutrient dynamics in upland forest streams.

Atmospheric deposition as a source of carbon and nutrients to barren, alpine soils of the Colorado Rocky Mountains

NASA Astrophysics Data System (ADS)

Mladenov, N.; Williams, M. W.; Schmidt, S. K.; Cawley, K.

2012-03-01

Many alpine areas are experiencing intense deglaciation, biogeochemical changes driven by temperature rise, and changes in atmospheric deposition. There is mounting evidence that the water quality of alpine streams may be related to these changes, including rising atmospheric deposition of carbon (C) and nutrients. Given that barren alpine soils can be severely C limited, we evaluated the magnitude and chemical quality of atmospheric deposition of C and nutrients to an alpine site, the Green Lake 4 catchment in the Colorado Rocky Mountains. Using a long term dataset (2002-2010) of weekly atmospheric wet deposition and snowpack chemistry, we found that volume weighted mean dissolved organic carbon (DOC) concentrations were approximately 1.0 mg L-1and weekly concentrations reached peaks as high at 6-10 mg L-1 every summer. Total dissolved nitrogen concentration also peaked in the summer, whereas total dissolved phosphorus and calcium concentrations were highest in the spring. Relationships among DOC concentration, dissolved organic matter (DOM) fluorescence properties, and nitrate and sulfate concentrations suggest that pollutants from nearby urban and agricultural sources and organic aerosols derived from sub-alpine vegetation may influence high summer DOC wet deposition concentrations. Interestingly, high DOC concentrations were also recorded during "dust-in-snow" events in the spring. Detailed chemical and spectroscopic analyses conducted for samples collected in 2010 revealed that the DOM in many late spring and summer samples was less aromatic and polydisperse and of lower molecular weight than that of winter and fall samples and, therefore, likely to be more bioavailable to microbes in barren alpine soils. Bioavailability experiments with different types of atmospheric C sources are needed to better evaluate the substrate quality of atmospheric C inputs. Our C budget estimates for the Green Lake 4 catchment suggest that atmospheric deposition represents an average input of approximately 13 kg C ha-1 yr-1 that could be as high as 24 kg C ha-1 yr-1 in high dust years and approaches that of autotrophic C fixation in barren soils.

Understanding DOC Mobilization Dynamics Through High Frequency Measurements in a Headwater Catchment

NASA Astrophysics Data System (ADS)

Werner, B.; Musolff, A.; Lechtenfeld, O.; de Rooij, G. H.; Fleckenstein, J. H.

2017-12-01

Increasing dissolved organic carbon (DOC) exports from headwater catchments impact the quality of downstream waters and pose challenges to water supply. The importance of riparian zones for DOC export from catchments in humid, temperate climates has generally been acknowledged, but the hydrological controls and biogeochemical factors that govern mobilization of DOC from riparian zones remain elusive. By analyzing high-frequency time series of UV-VIS based water quality we therefore aim at a better understanding on temporal dynamics of DOC mobilization and exports. In a first step a one year high frequency (15 minutes) data set from a headwater catchment in the Harz Mountains (Germany) was systematically analyzed for event-based patterns in DOC concentrations. Here, a simplistic linear model was generated to explain DOC concentration level and variability in the stream. Furthermore, spectral (e.g. slopes and SUVA254) and molecular (FT-ICR-MS) characterization of DOC was used to fingerprint in-stream DOC during events. Continuous DOC concentrations were best predicted (R², NSE = 0.53) by instantaneous discharge (Q) and antecede wetness conditions of the last 30 days (AWC30 = Precip.30/PET30) as well as mean air temperature (Tmean30) and mean discharge (Qmean30) of the preceding 30 days. Analyses of 36 events revealed seasonal trends for the slope, intercept and R² of linear log(DOC)-log(Q) regressions that can be best explained by the mean air temperature of the preceding 15 days. Continuously available optical DOC quality parameters SUVA254 and spectral slope (275 nm - 295 nm) systematically changed with shifts in discharge and in DOC concentration. This is underlined by selected FT-ICR-MS measurements indicating higher DOC aromaticity and oxygen content at high flow conditions. The change of DOC quality parameters during events indicate a shift in the activated source zones: DOC with a different quality was mobilized during high flow conditions when higher groundwater levels connected formerly disconnected DOC source zones to the stream. We conclude that the high concentration variability of DOC can be explained by a few controlling variables only. These variables can be linked to event-based DOC source activation and more seasonal controls of DOC production.

Experimental whole-lake increase of dissolved organic carbon concentration produces unexpected increase in crustacean zooplankton density

USGS Publications Warehouse

Kelly, Patrick T.; Craig, Nicola; Solomon, Christopher T.; Weidel, Brian C.; Zwart, Jacob A.; Jones, Stuart E.

2016-01-01

The observed pattern of lake browning, or increased terrestrial dissolved organic carbon (DOC) concentration, across the northern hemisphere has amplified the importance of understanding how consumer productivity varies with DOC concentration. Results from comparative studies suggest these increased DOC concentrations may reduce crustacean zooplankton productivity due to reductions in resource quality and volume of suitable habitat. Although these spatial comparisons provide an expectation for the response of zooplankton productivity as DOC concentration increases, we still have an incomplete understanding of how zooplankton respond to temporal increases in DOC concentration within a single system. As such, we used a whole-lake manipulation, in which DOC concentration was increased from 8 to 11 mg L−1 in one basin of a manipulated lake, to test the hypothesis that crustacean zooplankton production should subsequently decrease. In contrast to the spatially derived expectation of sharp DOC-mediated decline, we observed a small increase in zooplankton densities in response to our experimental increase in DOC concentration of the treatment basin. This was due to significant increases in gross primary production and resource quality (lower seston carbon-to-phosphorus ratio; C:P). These results demonstrate that temporal changes in lake characteristics due to increased DOC may impact zooplankton in ways that differ from those observed in spatial surveys. We also identified significant interannual variability across our study region, which highlights potential difficulty in detecting temporal responses of organism abundances to gradual environmental change (e.g., browning).

Sources of nitrate in snowmelt discharge: Evidence from water chemistry and stable isotopes of nitrate

USGS Publications Warehouse

Piatek, K.B.; Mitchell, M.J.; Silva, S.R.; Kendall, C.

2005-01-01

To determine whether NO3- concentration pulses in surface water in early spring snowmelt discharge are due to atmospheric NO 3-, we analyzed stream ??15N-NO 3- and ??18O-NO3- values between February and June of 2001 and 2002 and compared them to those of throughfall, bulk precipitation, snow, and groundwater. Stream total Al, DOC and Si concentrations were used to indicate preferential water flow through the forest floor, mineral soil, and ground water. The study was conducted in a 135-ha subcatchment of the Arbutus Watershed in the Huntington Wildlife Forest in the Adirondack Region of New York State, U.S.A. Stream discharge in 2001 increased from 0.6 before to 32.4 mm day-1 during snowmelt, and element concentrations increased from 33 to 71 ??mol L-1 for NO3-, 3 to 9 ??mol L-1 for total Al, and 330 to 570 ??mol L-1 for DOC. Discharge in 2002 was variable, with a maximum of 30 mm day-1 during snowmelt. The highest NO3-, Al, and DOC concentrations were 52, 10, and 630 ??mol L -1, respectively, and dissolved Si decreased from 148 ??mol L -1 before to 96 ??mol L-1 during snowmelt. Values of ??15N and ??18O of NO3- in stream water were similar in both years. Stream water, atmospherically- derived solutions, and groundwaters had overlapping ??15N- NO3- values. In stream and ground water, ??18O-NO3- values ranged from +5.9 to +12.9??? and were significantly lower than the +58.3 to +78.7??? values in atmospheric solutions. Values of ??18O-NO3- indicating nitrification, increase in Al and DOC, and decrease in dissolved Si concentrations indicating water flow through the soil suggested a dilution of groundwater NO3- by increasing contributions of forest floor and mineral soil NO3- during snowmelt. ?? Springer 2005.

Transport and Degradation of Dissolved Organic Matter and Associated Freshwater Pathways in the Laptev Sea (Siberian Arctic)

NASA Astrophysics Data System (ADS)

Hoelemann, J. A.; Janout, M. A.; Koch, B.; Bauch, D.; Novikhin, A.; Heim, B.; Eulenburg, A.; Kassens, H.; Timokhov, L.

2016-02-01

The Siberian shelves are seasonally ice-covered and characterized by large freshwater runoff rates from some of the largest rivers on earth. These rivers also provide a considerable amount of dissolved organic carbon (DOC) to the Arctic Ocean. With an annual load of about 6 Tg DOC a-1 the Lena River contributes nearly 20 percent of the annual DOC discharge to the Arctic Ocean. We present a comprehensive dataset collected during multiple Laptev Sea expeditions carried out in spring, summer and fall (2010-15) in order to explore the processes controlling the dispersal and degradation of DOM during the river water's passage across the shelf. Our investigations are focused on CDOM (Colored Dissolved Organic Matter), which resembles the DOC concentration, interacts with solar radiation and forms a major fraction of the organic matter pool. Our results show an inverse correlation between salinity and CDOM, which emphasizes its terrigenous source. Further, the spectral slope of CDOM absorption indicates that photochemical bleaching is the main process that reduces the CDOM absorption ( 20%) in freshwater along its transport across the shelf. The distribution of the Lena river water is primarily controlled by winds in summer. During summers with easterly or southerly winds, the plume remains on the central and northern Laptev shelf, and is available for export into the Arctic Basin. The CDOM-rich river water increases the absorption of solar radiation and enhances warming of a shallow surface layer. This emphasizes the importance of CDOM for sea surface temperatures and lateral ice melt on the shelf and adjacent basin. DOC concentrations in freshwater vary seasonally and become larger with increasing discharge. Our data indicate that the CDOM concentrations are highest during the freshet when landfast ice is still present. Subsequent mixing with local sea ice meltwater lowers CDOM to values that are characteristic for the Lena freshwater during the rest of the year.

Transport and degradation of dissolved organic matter and associated freshwater pathways in the Laptev Sea (Siberian Arctic)

NASA Astrophysics Data System (ADS)

Hoelemann, Jens; Janout, Markus; Koch, Boris; Bauch, Dorothea; Hellmann, Sebastian; Eulenburg, Antje; Heim, Birgit; Kassens, Heidemarie; Timokhov, leonid

2016-04-01

The Siberian shelves are seasonally ice-covered and characterized by large freshwater runoff rates from some of the largest rivers on earth. These rivers also provide a considerable amount of dissolved organic carbon (DOC) to the Arctic Ocean. With an annual load of about 6 Tg DOC a-1 the Lena River contributes nearly 20 percent of the annual DOC discharge to the Arctic Ocean. We present a comprehensive dataset collected during multiple Laptev Sea expeditions carried out in spring, summer and fall (2010-15) in order to explore the processes controlling the dispersal and degradation of DOM during the river water's passage across the shelf. Our investigations are focused on CDOM (Colored Dissolved Organic Matter), which resembles the DOC concentration, interacts with solar radiation and forms a major fraction of the organic matter pool. Our results show an inverse correlation between salinity and CDOM, which emphasizes its terrigenous source. Further, the spectral slope of CDOM absorption indicates that photochemical bleaching is the main process that reduces the CDOM absorption (~ 20%) in freshwater along its transport across the shelf. The distribution of the Lena river water is primarily controlled by winds in summer. During summers with easterly or southerly winds, the plume remains on the central and northern Laptev shelf, and is available for export into the Arctic Basin. The CDOM-rich river water increases the absorption of solar radiation and enhances warming of a shallow surface layer. This emphasizes the importance of CDOM for sea surface temperatures and lateral ice melt on the shelf and adjacent basin. DOC concentrations in freshwater vary seasonally and become larger with increasing discharge. Our data indicate that the CDOM concentrations are highest during the freshet when landfast ice is still present. Subsequent mixing with local sea ice meltwater lowers CDOM to values that are characteristic for the Lena freshwater during the rest of the year.

Minor contribution of small thaw ponds to the pools of carbon and methane in the inland waters of the permafrost-affected part of the Western Siberian Lowland

NASA Astrophysics Data System (ADS)

Polishchuk, Y. M.; Bogdanov, A. N.; Muratov, I. N.; Polishchuk, V. Y.; Lim, A.; Manasypov, R. M.; Shirokova, L. S.; Pokrovsky, O. S.

2018-04-01

Despite the potential importance of small (< 1000 m2) thaw ponds and thermokarst lakes in greenhouse gas (GHG) emissions from inland waters of high latitude and boreal regions, these features have not been fully inventoried and the volume of GHG and carbon in thermokarst lakes remains poorly constrained. This is especially true for the vast Western Siberia Lowland (WSL) which is subject to strong thermokarst activity. We assessed the number of thermokarst lakes and their size distribution for the permafrost-affected WSL territory based on a combination of medium-resolution Landsat-8 images and high-resolution Kanopus-V scenes on 78 test sites across the WSL in a wide range of lake sizes (from 20 to 2 × 108 m2). The results were in fair agreement with other published data for world lakes including those in circum-polar regions. Based on available measurements of CH4, CO2, and dissolved organic carbon (DOC) in thermokarst lakes and thaw ponds of the permafrost-affected part of the WSL, we found an inverse relationship between lake size and concentration, with concentrations of GHGs and DOC being highest in small thaw ponds. However, since these small ponds represent only a tiny fraction of the landscape (i.e. ~1.5% of the total lake area), their contribution to the total pool of GHG and DOC in inland lentic water of the permafrost-affected part of the WSL is less than 2%. As such, despite high concentrations of DOC and GHG in small ponds, their role in overall C storage can be negated. Ongoing lake drainage due to climate warming and permafrost thaw in the WSL may lead to a decrease in GHG emission potential from inland waters and DOC release from lakes to rivers.

Dissolved organic carbon in rainwater from areas heavily impacted by sugar cane burning

NASA Astrophysics Data System (ADS)

Coelho, C. H.; Francisco, J. G.; Nogueira, R. F. P.; Campos, M. L. A. M.

This work reports on rainwater dissolved organic carbon (DOC) from Ribeirão Preto (RP) and Araraquara over a period of 3 years. The economies of these two cities, located in São Paulo state (Brazil), are based on agriculture and related industries, and the region is strongly impacted by the burning of sugar cane foliage before harvesting. Highest DOC concentrations were obtained when air masses traversed sugar cane fields burned on the same day as the rain event. Significant increases in the DOC volume weighted means (VWM) during the harvest period, for both sites, and a good linear correlation ( r = 0.83) between DOC and K (a biomass burning marker) suggest that regional scale organic carbon emissions prevail over long-range transport. The DOC VWMs and standard deviations were 272 ± 22 μmol L -1 ( n = 193) and 338 ± 40 μmol L -1 ( n = 80) for RP and Araraquara, respectively, values which are at least two times higher than those reported for other regions influenced by biomass burning, such as the Amazon. These high DOC levels are discussed in terms of agricultural activities, particularly the large usage of biogenic fuels in Brazil, as well as the analytical method used in this work, which includes volatile organic carbon when reporting DOC values. Taking into account rainfall volume, estimated annual rainwater DOC fluxes for RP (4.8 g C m -2 yr -1) and Araraquara (5.4 g C m -2 yr -1) were close to that previously found for the Amazon region (4.8 g C m -2 yr -1). This work also discusses whether previous calculations of the global rainwater carbon flux may have been underestimated, since they did not consider large inputs from biomass combustion sources, and suffered from a possible analytical bias.

Water-soluble elements in snow and ice on Mt. Yulong.

PubMed

Niu, Hewen; Kang, Shichang; Shi, Xiaofei; He, Yuanqing; Lu, Xixi; Shi, Xiaoyi; Paudyal, Rukumesh; Du, Jiankuo; Wang, Shijin; Du, Jun; Chen, Jizu

2017-01-01

Melting of high-elevation glaciers can be accelerated by the deposition of light-absorbing aerosols (e.g., organic carbon, mineral dust), resulting in significant reductions of the surface albedo on glaciers. Organic carbon deposited in glaciers is of great significance to global carbon cycles, snow photochemistry, and air-snow exchange processes. In this work, various snow and ice samples were collected at high elevation sites (4300-4850masl) from Mt. Yulong on the southeastern Tibetan Plateau in 2015. These samples were analyzed for water-soluble organic carbon (DOC), total nitrogen (TN), and water-soluble inorganic ions (WSIs) to elucidate the chemical species and compositions of the glaciers in the Mt. Yulong region. Generally, glacial meltwater had the lowest DOC content (0.39mgL -1 ), while fresh snow had the highest (2.03mgL -1 ) among various types of snow and ice samples. There were obvious spatial and temporal trends of DOC and WSIs in glaciers. The DOC and TN concentrations decreased in the order of fresh snow, snow meltwater, snowpit, and surface snow, resulting from the photolysis of DOC and snow's quick-melt effects. The surface snow had low DOC and TN depletion ratios in the melt season; specifically, the ratios were -0.79 and -0.19mgL -1 d -1 , respectively. In the winter season, the ratios of DOC and TN were remarkably higher, with values of -0.20mgL -1 d -1 and -0.08mgL -1 d -1 , respectively. A reduction of the DOC and TN content in glaciers was due to snow's quick melt and sublimation. Deposition of these light-absorbing impurities (LAPs) in glaciers might accelerate snowmelt and even glacial retreat. Copyright © 2016 Elsevier B.V. All rights reserved.

Dissolved organic carbon and its potential predictors in eutrophic lakes.

PubMed

Toming, Kaire; Kutser, Tiit; Tuvikene, Lea; Viik, Malle; Nõges, Tiina

2016-10-01

Understanding of the true role of lakes in the global carbon cycle requires reliable estimates of dissolved organic carbon (DOC) and there is a strong need to develop remote sensing methods for mapping lake carbon content at larger regional and global scales. Part of DOC is optically inactive. Therefore, lake DOC content cannot be mapped directly. The objectives of the current study were to estimate the relationships of DOC and other water and environmental variables in order to find the best proxy for remote sensing mapping of lake DOC. The Boosted Regression Trees approach was used to clarify in which relative proportions different water and environmental variables determine DOC. In a studied large and shallow eutrophic lake the concentrations of DOC and coloured dissolved organic matter (CDOM) were rather high while the seasonal and interannual variability of DOC concentrations was small. The relationships between DOC and other water and environmental variables varied seasonally and interannually and it was challenging to find proxies for describing seasonal cycle of DOC. Chlorophyll a (Chl a), total suspended matter and Secchi depth were correlated with DOC and therefore are possible proxies for remote sensing of seasonal changes of DOC in ice free period, while for long term interannual changes transparency-related variables are relevant as DOC proxies. CDOM did not appear to be a good predictor of the seasonality of DOC concentration in Lake Võrtsjärv since the CDOM-DOC coupling varied seasonally. However, combining the data from Võrtsjärv with the published data from six other eutrophic lakes in the world showed that CDOM was the most powerful predictor of DOC and can be used in remote sensing of DOC concentrations in eutrophic lakes. Copyright © 2016 Elsevier Ltd. All rights reserved.

Influence of natural dissolved organic carbon on the bioavailability of mercury to a freshwater alga

USGS Publications Warehouse

Gorski, P.R.; Armstrong, D.E.; Hurley, J.P.; Krabbenhoft, D.P.

2008-01-01

Bioavailability of mercury (Hg) to Selenastrum capricornutum was assessed in bioassays containing field-collected freshwater of varying dissolved organic carbon (DOC) concentrations. Bioconcentration factor (BCF) was measured using stable isotopes of methylmercury (MeHg) and inorganic Hg(II). BCFs for MeHg in low-DOC lake water were significantly larger than those in mixtures of lake water and high-DOC river water. The BCF for MeHg in rainwater (lowest DOC) was the largest of any treatment. Rainwater and lake water also had larger BCFs for Hg(II) than river water. Moreover, in freshwater collected from several US and Canadian field sites, BCFs for Hg(II) and MeHg were low when DOC concentrations were >5 mg L-1. These results suggest high concentrations of DOC inhibit bioavailability, while low concentrations may provide optimal conditions for algal uptake of Hg. However, variability of BCFs at low DOC indicates that DOC composition or other ligands may determine site-specific bioavailability of Hg.

Hydro-ecological controls on dissolved carbon dynamics in groundwater and export to streams in a temperate pine forest

NASA Astrophysics Data System (ADS)

Deirmendjian, Loris; Loustau, Denis; Augusto, Laurent; Lafont, Sébastien; Chipeaux, Christophe; Poirier, Dominique; Abril, Gwenaël

2018-02-01

We studied the export of dissolved inorganic carbon (DIC) and dissolved organic carbon (DOC) from forested shallow groundwater to first-order streams, based on groundwater and surface water sampling and hydrological data. The selected watershed was particularly convenient for such study, with a very low slope, with pine forest growing on sandy permeable podzol and with hydrology occurring exclusively through drainage of shallow groundwater (no surface runoff). A forest plot was instrumented for continuous eddy covariance measurements of precipitation, evapotranspiration, and net ecosystem exchanges of sensible and latent heat fluxes as well as CO2 fluxes. Shallow groundwater was sampled with three piezometers located in different plots, and surface waters were sampled in six first-order streams; river discharge and drainage were modeled based on four gauging stations. On a monthly basis and on the plot scale, we found a good consistency between precipitation on the one hand and the sum of evapotranspiration, shallow groundwater storage and drainage on the other hand. DOC and DIC stocks in groundwater and exports to first-order streams varied drastically during the hydrological cycle, in relation with water table depth and amplitude. In the groundwater, DOC concentrations were maximal in winter when the water table reached the superficial organic-rich layer of the soil. In contrast, DIC (in majority excess CO2) in groundwater showed maximum concentrations at low water table during late summer, concomitant with heterotrophic conditions of the forest plot. Our data also suggest that a large part of the DOC mobilized at high water table was mineralized to DIC during the following months within the groundwater itself. In first-order streams, DOC and DIC followed an opposed seasonal trend similar to groundwater but with lower concentrations. On an annual basis, leaching of carbon to streams occurred as DIC and DOC in similar proportion, but DOC export occurred in majority during short periods of the highest water table, whereas DIC export was more constant throughout the year. Leaching of forest carbon to first-order streams represented a small portion (approximately 2 %) of the net land CO2 sink at the plot. In addition, approximately 75 % of the DIC exported from groundwater was not found in streams, as it returned very fast to the atmosphere through CO2 degassing.

Seasonality of major redox constituents in a shallow subterranean estuary

NASA Astrophysics Data System (ADS)

O'Connor, Alison E.; Krask, Julie L.; Canuel, Elizabeth A.; Beck, Aaron J.

2018-03-01

The subterranean estuary (STE), the subsurface mixing zone of outflowing fresh groundwater and infiltrating seawater, is an area of extensive geochemical reactions that determine the composition of groundwater that flows into coastal environments. This study examined the porewater composition of a shallow STE (<5 m depth) in Gloucester Point, VA (USA) over two years to determine seasonal variations in dissolved organic carbon (DOC) and the reduced metabolites Fe, Mn, and sulfide. An additional aim of this study was to investigate the relative importance of salinity gradients (which have great geochemical influence in surface estuaries) versus redox gradients on STE geochemistry. Two freshwater endmembers were identified, between which redox potential and composition varied with depth-a shallow freshwater endmember was oxidizing and high in DOC, whereas a deep freshwater endmember was reducing, lower in DOC, and high in sulfide. Results showed that dissolved Fe, Mn, and sulfide varied along a redox gradient distinct from the salinity gradient, and that three-endmember mixing was required to quantify non-conservative chemical addition/removal in the STE. In addition to salinity, humic carbon was used as a quasi-conservative tracer to quantify mixing according to a three-endmember model. The vertical distributions of DOC and reduced metabolites remained approximately constant over time, but concentrations varied with season. Dissolved organic carbon concentrations were greatest in the summer, and shallow meteoric groundwater supplied the majority of DOC to the STE. In summer, there was additional evidence for shallow non-conservative addition of DOC. Dissolved Fe and Mn were highest in a subsurface plume through the middle of the STE (100-140 cm below sediment surface at the high tide line) which was characterized by higher concentrations and greater non-conservative addition in the winter. In contrast, sulfide was higher in summer at depths within the Fe and Mn plume (100-140 cm). We attribute the contrasting seasonal patterns of dissolved Fe, Mn, and sulfide to differences in microbial response to temperature changes and organic matter availability, and to competition at the ferrous-sulfidic transition zone between dissimilatory metal reduction and sulfate reduction, leading to sulfate/sulfur reducing bacteria (SRB) being more active in summer and metal reducers being more active in winter. Throughout the STE, seasonal temperature and DOC variations determined the spatial distribution and geochemical cycling of Fe, Mn, and sulfur.

Chemical characteristics of particulate, colloidal, and dissolved organic material in Loch Vale Watershed, Rocky Mountain National Park

USGS Publications Warehouse

McKnight, Diane M.; Harnish, R.; Wershaw, R. L.; Baron, Jill S.; Schiff, S.

1997-01-01

The chemical relationships among particulate and colloidal organic material and dissolved fulvic acid were examined in an alpine and subalpine lake and two streams in Loch Vale Watershed, Rocky Mountain National Park. The alpine lake, Sky Pond, had the lowest dissolved organic carbon (DOC) (0.37 mgC/L), the highest particulate carbon (POC) (0.13 mgC/L), and high algal biomass. The watershed of Sky Pond is primarily talus slope, and DOC and POC may be autochthonous. Both Andrews Creek and Icy Brook gain DOC as they flow through wet sedge meadows. The subalpine lake, The Loch, receives additional organic material from the surrounding forest and had a higher DOC (0.66 mgC/L). Elemental analysis, stable carbon isotopic compositon, and 13C-NMR characterization showed that: 1) particulate material had relatively high inorganic contents and was heterogeneous in compositon, 2) colloidal material was primarily carbohydrate material with a low inorganic content at all sites; and 3) dissolved fulvic acid varied in compositon among sites. The low concentration and carbohydrate-rich character of the colloidal material suggests that this fraction is labile to microbial degradation and may be turning over more rapidly than particulate fractions or dissolved fulvic acid. Fulvic acid from Andrews Creek had the lowest N content and aromaticity, whereas Sky Pond fulvic acid had a higher N content and lower aromaticity than fulvic acid from The Loch. The UV-visible spectra of the fulvic acids demonstrate that variation in characteristics with sources of organic carbon can explain to some extent the observed nonlinear relationship between UV-B extinction coefficients and DOC concentrations in lakes.

Adsorption-desorption of dimethenamid and fenarimol onto three agricultural soils as affected by treated wastewater and fresh sewage sludge-derived dissolved organic carbon.

PubMed

Rodríguez-Liébana, José Antonio; Peña, Aránzazu

2018-07-01

The use of treated wastewaters (TWW) in agriculture is widening in areas suffering drought, such as southern Europe, to preserve freshwater supply for human consumption. The composition of TWW, especially concerning their organic carbon (OC) content, has been demonstrated to influence the processes governing the behavior of non-ionic pesticides in soils. Three OC-poor agricultural soils (SV, RM1 and RM3) from the province of Granada (Spain) were chosen for the assessment of the adsorption and desorption of the herbicide dimethenamid (DIM) and the fungicide fenarimol (FEN). TWW and sewage sludge extracts at different dissolved OC (DOC) concentrations (30, 90 and 300 mg L -1 ) were considered to evaluate their effect on pesticide adsorption-desorption. As expected by their properties, DIM and FEN were weakly and moderately adsorbed to the soils, respectively. Soil OC seemed to be the major factor controlling FEN adsorption, whereas the mineral fraction played a key role in DIM adsorption, especially in RM1 with high clay:OC ratio. Although TWW did not significantly modify the adsorption of pesticides, it enhanced DIM desorption from the three soils. Adsorption of FEN to SV and RM3 was directly related to the concentration of DOC, possibly due to co-sorption phenomena. Hysteretic desorption was found in all cases, indicating partially reversible adsorption. While FEN desorption was not altered by the solutions, the use of sludge extracts at the highest DOC concentration (300 mg L -1 ) enhanced DIM desorption as occurred with TWW. Interactions with DOC in solution seemed to predominate for this less hydrophobic compound, thus increasing the risk of natural waters contamination if TWW will be used. Copyright © 2018 Elsevier Ltd. All rights reserved.

Linking the mobilization of dissolved organic matter in catchments and its removal in drinking water treatment to its molecular characteristics.

PubMed

Raeke, Julia; Lechtenfeld, Oliver J; Tittel, Jörg; Oosterwoud, Marieke R; Bornmann, Katrin; Reemtsma, Thorsten

2017-04-15

Drinking water reservoirs in the Northern Hemisphere are largely affected by the decadal-long increase in riverine dissolved organic carbon (DOC) concentrations. The removal of DOC in drinking water treatment is costly and predictions are needed to link DOC removal efficiency to its mobilization in catchments, both of which are determined by the molecular composition. To study the effect of hydrological events and land use on the molecular characteristics of dissolved organic matter (DOM), 36 samples from three different catchment areas in the German low mountain ranges, with DOC concentrations ranging from 3 to 32 mg L -1 , were examined. Additionally, nine pairs of samples from downstream drinking water reservoirs were analyzed before and after flocculation. The molecular composition and the age of DOM were analyzed using ultrahigh resolution Fourier transform ion cyclotron resonance mass spectrometry (FTICR-MS) and radiocarbon ( 14 C) analysis. At elevated discharge in a forested catchment comparatively younger, more oxygenated and unsaturated molecules of higher molecular weight were preferentially mobilized, likely linked to the reductive mobilization of iron. DOM with highly similar molecular characteristics (O/C ratio > 0.5, m/z > 500) could also be efficiently removed through flocculation in drinking water treatment. The proportion of DOM removed through flocculation ranged between 43% and 73% of DOC and was highest at elevated discharge. In catchment areas with a higher percentage of grassland and agriculture a higher proportion of DOM molecules containing sulfur and nitrogen was detected, which in turn could be less efficiently flocculated. Altogether, it was shown that DOM that is released during large hydrological events can be efficiently flocculated again, suggesting a reversal of similar chemical mechanisms in both processes. Since the occurrence of heavy rainfall events is predicted to increase in the future, event-driven mobilization of DOC may continue to challenge drinking water production. Copyright © 2017 Elsevier Ltd. All rights reserved.

Distribution characteristics of dissolved organic carbon in annular wetland soil-water solutions through soil profiles in the Sanjiang Plain, northeast China.

PubMed

Xi, Min; Lu, Xian-Guo; Li, Yue; Kong, Fan-Long

2007-01-01

Overwhelming evidence reveals that concentrations of dissolved organic carbon (DOC) have increased in streams which brings negative environmental impacts. DOC in stream flow is mainly originated from soil-water solutions of watershed. Wetlands prove to be the most sensitive areas as an important DOC reserve between terrestrial and fluvial biogeosystems. This reported study was focused on the distribution characteristics and the controlling factors of DOC in soil-water solutions of annular wetland, i.e., a dishing wetland and a forest wetland together, in the Sanjiang Plain, Northeast China. The results indicate that DOC concentrations in soil-water solutions decreased and then increased with increasing soil depth in the annular wetland. In the upper soil layers of 0-10 cm and 10-20 cm, DOC concentrations in soil-water solutions linearly increased from edge to center of the annular wetland (R2 = 0.3122 and R2 = 0.443). The distribution variations were intimately linked to DOC production and utilization and DOC transport processes in annular wetland soil-water solutions. The concentrations of total organic carbon (TOC), total carbon (TC) and Fe(II), DOC mobility and continuous vertical and lateral flow affected the distribution variations of DOC in soil-water solutions. The correlation coefficients between DOC concentrations and TOC, TC and Fe(II) were 0.974, 0.813 and 0.753 respectively. These distribution characteristics suggested a systematic response of the distribution variations of DOC in annular wetland soil-water solutions to the geometry of closed depressions on a scale of small catchments. However, the DOC in soil pore water of the annular wetland may be the potential source of DOC to stream flow on watershed scale. These observations also implied the fragmentation of wetland landscape could bring the spatial-temporal variations of DOC distribution and exports, which would bring negative environmental impacts in watersheds of the Sanjiang Plain.

Pathways for arsenic from sediments to groundwater to streams: Biogeochemical processes in the Inner Coastal Plain, New Jersey, USA

USGS Publications Warehouse

Barringer, Julia L.; Mumford, Adam; Young, Lily Y.; Reilly, Pamela A.; Bonin, Jennifer L.; Rosman, Robert

2010-01-01

The Cretaceous and Tertiary sediments that underlie the Inner Coastal Plain of New Jersey contain the arsenic-rich mineral glauconite. Streambed sediments in two Inner Coastal Plain streams (Crosswicks and Raccoon Creeks) that traverse these glauconitic deposits are enriched in arsenic (15–25 mg/kg), and groundwater discharging to the streams contains elevated levels of arsenic (>80 μg/L at a site on Crosswicks Creek) with arsenite generally the dominant species. Low dissolved oxygen, low or undetectable levels of nitrate and sulfate, detectable sulfide concentrations, and high concentrations of iron and dissolved organic carbon (DOC) in the groundwater indicate that reducing environments are present beneath the streambeds and that microbial activity, fueled by the DOC, is involved in releasing arsenic and iron from the geologic materials. In groundwater with the highest arsenic concentrations at Crosswicks Creek, arsenic respiratory reductase gene (arrA) indicated the presence of arsenic-reducing microbes. From extracted DNA, 16s rRNA gene sequences indicate the microbial community may include arsenic-reducing bacteria that have not yet been described. Once in the stream, iron is oxidized and precipitates as hydroxide coatings on the sediments. Arsenite also is oxidized and co-precipitates with or is sorbed to the iron hydroxides. Consequently, dissolved arsenic concentrations are lower in streamwater than in the groundwater, but the arsenic contributed by groundwater becomes part of the arsenic load in the stream when sediments are suspended during high flow. A strong positive relation between concentrations of arsenic and DOC in the groundwater samples indicates that any process—natural or anthropogenic—that increases the organic carbon concentration in the groundwater could stimulate microbial activity and thus increase the amount of arsenic that is released from the geologic materials.

Response Characteristics of Dissolved Organic Carbon Flushing in a Subarctic Alpine Catchment

NASA Astrophysics Data System (ADS)

Carey, S. K.

2002-12-01

Dissolved organic carbon (DOC) is an important part of ecosystem-scale carbon balances and in the transport of contaminants as it interacts with other dissolved substances including trace metals. It also can be used as a surrogate hydrological tracer in permafrost regions as near-surface waters are often DOC enriched due to the presence of thick organic soils. In a small subarctic alpine catchment within the Wolf Creek Research Basin, Yukon, Canada, DOC was studied in the summer of 2001 and spring of 2002 to determine the role frost (both permanent and seasonal), snowmelt and summer storms on DOC flushing. Peak DOC concentrations occurred during the snowmelt period, approximately one week prior to peak discharge. However, peak discharge took place several weeks after snow on south facing exposures had melted. Within the hillslopes, DOC concentrations were three to five times greater in wells underlain with permafrost compared with seasonal frost. Groundwater DOC concentrations declined during snowmelt, yet remained at levels above the streamflow. After peaking, streamflow DOC concentrations declined exponentially suggesting a simple flushing mechanism, however there did not appear to be a relation between DOC and topographic position. Following melt, permafrost underlain slopes had near-surface water tables and retained elevated levels of DOC, whereas slopes without permafrost had rapidly declining water tables at upslope locations with low DOC concentrations at all positions except near-stream riparian zones. The influence of summer rainstorms on DOC was monitored on three occasions. In each case DOC peaked on the ascending limb of the runoff hydrograph and declined exponentially on the receding limb and hysteretic behavior occurred between discharge and DOC during all events. Patterns of DOC within the hillslopes and streams suggest that runoff from permafrost-underlain slopes control DOC flushing within the stream during both snowmelt and summer periods. This flushing mechanism conforms with conceptual models of runoff generation in discontinuous permafrost catchments whereby water tables within permafrost-underlain slopes rise into porous organic-layers, whereupon DOC is leached into the water and rapidly conveyed to the stream.

Factors Controlling Methane in Arctic Lakes of Southwest Greenland

PubMed Central

2016-01-01

We surveyed 15 lakes during the growing season of 2014 in Arctic lakes of southwest Greenland to determine which factors influence methane concentrations in these systems. Methane averaged 2.5 μmol L-1 in lakes, but varied a great deal across the landscape with lakes on older landscapes farther from the ice sheet margin having some of the highest values of methane reported in lakes in the northern hemisphere (125 μmol L-1). The most important factors influencing methane in Greenland lakes included ionic composition (SO4, Na, Cl) and chlorophyll a in the water column. DOC concentrations were also related to methane, but the short length of the study likely underestimated the influence and timing of DOC on methane concentrations in the region. Atmospheric methane concentrations are increasing globally, with freshwater ecosystems in northern latitudes continuing to serve as potentially large sources in the future. Much less is known about how freshwater lakes in Greenland fit in the global methane budget compared to other, more well-studied areas of the Arctic, hence our work provides essential data for a more complete view of this rapidly changing region. PMID:27454863

Characterising Event-Based DOM Inputs to an Urban Watershed

NASA Astrophysics Data System (ADS)

Croghan, D.; Bradley, C.; Hannah, D. M.; Van Loon, A.; Sadler, J. P.

2017-12-01

Dissolved Organic Matter (DOM) composition in urban streams is dominated by terrestrial inputs after rainfall events. Urban streams have particularly strong terrestrial-riverine connections due to direct input from terrestrial drainage systems. Event driven DOM inputs can have substantial adverse effects on water quality. Despite this, DOM from important catchment sources such as road drains and Combined Sewage Overflows (CSO's) remains poorly characterised within urban watersheds. We studied DOM sources within an urbanised, headwater watershed in Birmingham, UK. Samples from terrestrial sources (roads, roofs and a CSO), were collected manually after the onset of rainfall events of varying magnitude, and again within 24-hrs of the event ending. Terrestrial samples were analysed for fluorescence, absorbance and Dissolved Organic Carbon (DOC) concentration. Fluorescence and absorbance indices were calculated, and Parallel Factor Analysis (PARAFAC) was undertaken to aid sample characterization. Substantial differences in fluorescence, absorbance, and DOC were observed between source types. PARAFAC-derived components linked to organic pollutants were generally highest within road derived samples, whilst humic-like components tended to be highest within roof samples. Samples taken from the CSO generally contained low fluorescence, however this likely represents a dilution effect. Variation within source groups was particularly high, and local land use seemed to be the driving factor for road and roof drain DOM character and DOC quantity. Furthermore, high variation in fluorescence, absorbance and DOC was apparent between all sources depending on event type. Drier antecedent conditions in particular were linked to greater presence of terrestrially-derived components and higher DOC content. Our study indicates that high variations in DOM character occur between source types, and over small spatial scales. Road drains located on main roads appear to contain the poorest quality DOM of the sources studied due to the presence of hydrocarbons. In order to prevent storm-derived DOM degradation of water quality of urban streams, greater knowledge of links between these drainage sources, and their pathways to streams is required.

Dissolved organic carbon reduces the toxicity of copper to germlings of the macroalgae, Fucus vesiculosus.

PubMed

Brooks, Steven J; Bolam, Thi; Tolhurst, Laura; Bassett, Janice; La Roche, Jay; Waldock, Mike; Barry, Jon; Thomas, Kevin V

2008-05-01

This study investigates the effects of waterborne copper exposure on germling growth in chemically defined seawater. Germlings of the macroalgae, Fucus vesiculosus were exposed to a range of copper and dissolved organic carbon (DOC as humic acid) concentrations over 14 days. Germling growth was found to be a sensitive indicator of copper exposure with total copper (TCu) and labile copper (LCu) EC(50) values of approximately 40 and 20 microg/L, respectively, in the absence of added DOC. The addition of DOC into the exposure media provided germlings with protection against copper toxicity, with an increased TCu EC(50) value of 117.3 microg/L at a corrected DOC (cDOC from humic acid only) concentration of 2.03 mg/L. The LCu EC(50) was not affected by a cDOC concentration of 1.65 mg/L or less, suggesting that the LCu concentration not the TCu concentration was responsible for inhibiting germling growth. However, at a cDOC concentration of approximately 2mg/L an increase in the LCu EC(50) suggests that the LCu concentration may play a role in the overall toxicity to the germlings. This is contrary to current understanding of aquatic copper toxicity and possible explanations for this are discussed.

Spatio-temporal variability of dissolved organic nitrogen (DON), carbon (DOC), and nutrients in the Nile River, Egypt.

PubMed

Badr, El-Sayed A

2016-10-01

Increases in human activity have resulted in enhanced anthropogenic inputs of nitrogen (N) and carbon (C) into the Nile River. The Damietta Branch of the Nile is subject to inputs from industrial, agricultural, and domestic wastewater. This study investigated the distribution and seasonality of dissolved organic nitrogen (DON), dissolved organic carbon (DOC), and nutrients in the Nile Damietta Branch. Water samples were collected from 24 sites between May 2009 and February 2010. Dissolved organic nitrogen concentrations averaged 251 ± 115 μg/l, with a range of 90.2-671 μg/l, and contributed 40.8 ± 17.7 % to the total dissolved nitrogen (TDN) pool. Relative to autumn and winter, DON was a larger fraction of the TDN pool during spring and summer indicating the influence of bacterioplankton on the nitrogen cycle. Concentrations of DOC ranged from 2.23 to 11.3 mg/l with an average of 5.15 ± 2.36 mg/l, reflecting a high organic matter load from anthropogenic sources within the study area, and were highest during autumn. Higher values of biochemical oxygen demand (BOD), chemical oxygen demand (COD), DON, nitrate, and phosphate occurred downstream of the Damietta Branch and were probably due to anthropogenic inputs to the Nile from the Damietta district. A bacterial incubation experiment indicated that 52.1-95.0 % of DON was utilized by bacteria within 21 days. The decrease in DON concentration was accompanied by an increase in nitrate concentration of 54.8-87.3 %, presumably through DON mineralization. Based on these results, we recommend that water quality assessments consider DON and DOC, as their omission may result in an underestimation of the total organic matter load and impact.

Mercury cycling in stream ecosystems. 2. Benthic methylmercury production and bed sediment-pore water partitioning.

PubMed

Marvin-Dipasquale, Mark; Lutz, Michelle A; Brigham, Mark E; Krabbenhoft, David P; Aiken, George R; Orem, William H; Hall, Britt D

2009-04-15

Mercury speciation, controls on methylmercury (MeHg) production, and bed sediment-pore water partitioning of total Hg (THg) and MeHg were examined in bed sediment from eight geochemically diverse streams where atmospheric deposition was the predominant Hg input. Across all streams, sediment THg concentrations were best described as a combined function of sediment percent fines (%fines; particles < 63 microm) and organic content. MeHg concentrations were best described as a combined function of organic content and the activity of the Hg(II)-methylating microbial community and were comparable to MeHg concentrations in streams with Hg inputs from industrial and mining sources. Whole sediment tin-reducible inorganic reactive Hg (Hg(II)R) was used as a proxy measure for the Hg(II) pool available for microbial methylation. In conjunction with radiotracer-derived rate constants of 203Hg(II) methylation, Hg(II)R was used to calculate MeHg production potential rates and to explain the spatial variability in MeHg concentration. The %Hg(II)R (of THg) was low (2.1 +/- 5.7%) and was inversely related to both microbial sulfate reduction rates and sediment total reduced sulfur concentration. While sediment THg concentrations were higher in urban streams, %MeHg and %Hg(II)R were higher in nonurban streams. Sediment pore water distribution coefficients (log Kd's) for both THg and MeHg were inversely related to the log-transformed ratio of pore water dissolved organic carbon (DOC) to bed sediment %fines. The stream with the highest drainage basin wetland density also had the highest pore water DOC concentration and the lowest log Kd's for both THg and MeHg. No significant relationship existed between overlying water MeHg concentrations and those in bed sediment or pore water, suggesting upstream sources of MeHg production may be more important than local streambed production as a driver of water column MeHg concentration in drainage basins that receive Hg inputs primarily from atmospheric sources.

Drought causes step-changes in catchment-scale carbon export from peatland catchments

NASA Astrophysics Data System (ADS)

Howden, Nicholas; Worrall, Fred; Burt, Tim

2015-04-01

Increases in fluvial DOC concentrations in world rivers, particularly those that drain areas of peatland, have been observed for some years, suggesting an increase in carbon loss from the terrestrial biosphere. But it has not been straightforward to identify what causes these increases due to a lack of long-term time series to characterise both observed DOC concentrations and potential drivers. The York Waterworks Company (York, UK) abstracted drinking water from the Yorkshire Ouse just upstream of the city from the late 1800s until 2002. During the period August 1945 to December 2002, records of monthly-average DOC concentrations were kept (using water colour as a surrogate). From January 2003 onwards, the Environment Agency of England and Wales (EA) continued the monitoring, thus providing a 68-year record of monthly-average DOC concentrations in the Yorkshire Ouse, which is the longest DOC time series ever reported for a catchment with significant peat cover. We use the Yorkshire Ouse DOC record to develop a new method that shows how changes in DOC concentration and river flow have influenced carbon fluxes in the Ouse for the latter half of the 20th century and show that the only major changes in DOC flux are caused by step-increases in concentration following severe drought. We then use this method to identify a similar effect in other DOC records for UK rivers. The results suggest that increases in DOC export are due more to discrete events than to the impact of continuous drivers (such as increasing temperatures or changing atmospheric deposition), and also show these increases not to be reversed for at least four decades.

Long-term anoxia and release of ancient, labile carbon upon thaw of Pleistocene permafrost

USGS Publications Warehouse

Ewing, Stephanie A.; O'Donnell, Jonathan A.; Aiken, George R.; Butler, Kenna D.; Butman, David; Windham-Myers, Lisamarie; Kanevskiy, Mikhail

2015-01-01

The fate of permafrost carbon upon thaw will drive feedbacks to climate warming. Here we consider the character and context of dissolved organic carbon (DOC) in yedoma permafrost cores from up to 20 m depth in central Alaska. We observed high DOC concentrations (4 to 129 mM) and consistent low molecular weight organic acid concentrations in three cores. We estimate a DOC production rate of 12 µmol DOC m−2 yr−1 based on model ages of up to ~200 kyr derived from uranium isotopes. Acetate C accounted for 24 ± 1% of DOC in all samples. This proportion suggests long-term anaerobiosis and is likely to influence thaw outcomes due to biolability of acetate upon release in many environments. The combination of uranium isotopes, ammonium concentrations, and calcium concentrations explained 86% of the variation in thaw water DOC concentrations, suggesting that DOC production may be related to both reducing conditions and mineral dissolution over time.

Re-evaluation of colorimetric Cl- data from natural waters with DOC

USGS Publications Warehouse

Norton, S.A.; Handlet, M.J.; Kahl, J.S.; Peters, N.E.

1996-01-01

Colorimetric Cl- data from natural solutions that contain dissolved organic carbon (DOC) may be biased high. We evaluated aquatic Cl- concentrations in ecosystem compartments at the Bear Brook Watershed, Maine, and from lakes in Maine, using ion chromatography and colorimetry. DOC imparts a positive interference on colorimetric Cl- results proportional to DOC concentrations at approximately 0.8 ??eq Cl-/L per mg DOC/L. The interference is not a function of Cl- concentration. The resulting bias in concentrations of Cl- may be 50% or more of typical environmental values for Cl- in areas remote from atmospheric deposition of marine aerosols. Such biased data in the literature appear to have led to spurious conclusions about recycling of Cl- by forests, the usefulness of Cl- as a conservative tracer in watershed studies, and calculations of elemental budgets, ion balance, charge density of DOC, and dry deposition factors.

Role of Fire and Landscape Position on Dissolved Organic Carbon Composition and Reactivity in the Yukon-Kuskokwim Delta, Alaska

NASA Astrophysics Data System (ADS)

Bristol, E. M.; Dabrowski, J. S.; Jimmie, J. A.; Peter, D. L.; Holmes, R. M.; Mann, P. J.; Natali, S.; Schade, J. D.

2017-12-01

The Yukon-Kuskokwim Delta in southwest, Alaska is characterized by discontinuous permafrost, which is vulnerable to thaw induced by climate change. Recent fires in the delta have caused dramatic changes in the landscape, likely changing carbon dynamics, and potentially altering dissolved organic carbon (DOC) composition and DOC concentrations in aquatic ecosystems. These changes, in turn, likely affect microbial respiration and hydrologic C export from watersheds in the delta. In this study, we investigated how landscape position and fire history drive changes in DOC composition and reactivity in aquatic ecosystems. We surveyed soil pore waters, ponds, fens, and streams at varying landscape positions in burned and unburned landscapes. We also conducted a laboratory experiment to compare the role of photooxidation, photodegradation, and microbial respiration in altering DOC composition and concentration. Surface waters in burned regions were higher in temperature and inorganic nitrogen concentrations. Higher conductivity in burned areas suggests that fire is deepening the water table, causing water to flow through a more mineral soil horizon. While DOC concentrations did not vary significantly by landscape position or fire history, optical properties of DOC suggest that DOC molecular weight is lower in burned regions and decreases along flow paths. Similarly, our incubation experiment indicated that changes in DOC composition are driven by exposure to light more than bacterial respiration, and that photochemical reactivity declines along flow paths. Percent DOC loss was greatest in waters exposed to both light and bacterial, and percent DOC loss from burned watershed waters was correlated with optical properties. Based on our findings, we predict that the combination of increased surface water temperatures, increased inorganic nitrogen concentrations, and lower molecular weight DOC will increase bacterial respiration of DOC in watersheds burned by wildfire. Further research is needed to better understand the changing hydrology in burned tundra, and the relationship between photooxidation and biological mineralization of DOC.

High soil solution carbon and nitrogen concentrations in a drained Atlantic bog are reduced to natural levels by 10 years of rewetting

NASA Astrophysics Data System (ADS)

Frank, S.; Tiemeyer, B.; Gelbrecht, J.; Freibauer, A.

2014-04-01

Anthropogenic drainage of peatlands releases additional greenhouse gases to the atmosphere, and dissolved carbon (C) and nutrients to downstream ecosystems. Rewetting drained peatlands offers a possibility to reduce nitrogen (N) and C losses. In this study, we investigate the impact of drainage and rewetting on the cycling of dissolved C and N as well as on dissolved gases, over a period of 1 year and a period of 4 months. We chose four sites within one Atlantic bog complex: a near-natural site, two drained grasslands with different mean groundwater levels and a former peat cutting area rewetted 10 years ago. Our results clearly indicate that long-term drainage has increased the concentrations of dissolved organic carbon (DOC), ammonium, nitrate and dissolved organic nitrogen (DON) compared to the near-natural site. DON and ammonium contributed the most to the total dissolved nitrogen. Nitrate concentrations below the mean groundwater table were negligible. The concentrations of DOC and N species increased with drainage depth. In the deeply-drained grassland, with a mean annual water table of 45 cm below surface, DOC concentrations were twice as high as in the partially rewetted grassland with a mean annual water table of 28 cm below surface. The deeply drained grassland had some of the highest-ever observed DOC concentrations of 195.8 ± 77.3 mg L-1 with maximum values of >400 mg L-1. In general, dissolved organic matter (DOM) at the drained sites was enriched in aromatic moieties and showed a higher degradation status (lower DOC to DON ratio) compared to the near-natural site. At the drained sites, the C to N ratios of the uppermost peat layer were the same as of DOM in the peat profile. This suggests that the uppermost degraded peat layer is the main source of DOM. Nearly constant DOM quality through the profile furthermore indicated that DOM moving downwards through the drained sites remained largely biogeochemically unchanged. Unlike DOM concentration, DOM quality and dissolved N species distribution were similar in the two grasslands and thus unaffected by the drainage depth. Methane production during the winter months at the drained sites was limited to the subsoil, which was quasi-permanently water saturated. The recovery of the water table in the winter months led to the production of nitrous oxide around mean water table depth at the drained sites. The rewetted and the near-natural site had comparable DOM quantity and quality (DOC to DON ratio and aromaticity). 10 years after rewetting quasi-pristine biogeochemical conditions have been re-established under continuously water logged conditions in the former peat cut area. Only the elevated dissolved methane and ammonium concentrations reflected the former disturbance by drainage and peat extraction. Rewetting via polder technique seems to be an appropriate way to revitalize peatlands on longer timescales and to improve the water quality of downstream water bodies.

Stoichiometric determination of nitrate fate in agricultural ecosystems during rainfall events.

PubMed

Xu, Zuxin; Wang, Yiyao; Li, Huaizheng

2015-01-01

Ecologists have found a close relationship between the concentrations of nitrate (NO3-) and dissolved organic carbon (DOC) in ecosystems. However, it is difficult to determine the NO3- fate exactly because of the low coefficient in the constructed relationship. In the present paper, a negative power-function equation (r(2) = 0.87) was developed by using 411 NO3- data points and DOC:NO3- ratios from several agricultural ecosystems during different rainfall events. Our analysis of the stoichiometric method reveals several observations. First, the NO3- concentration demonstrated the largest changes when the DOC:NO3- ratio increased from 1 to 10. Second, the biodegradability of DOC was an important factor in controlling the NO3- concentration of agricultural ecosystems. Third, sediment was important not only as a denitrification site, but also as a major source of DOC for the overlying water. Fourth, a high DOC concentration was able to maintain a low NO3- concentration in the groundwater. In conclusion, this new stoichiometric method can be used for the accurate estimation and analysis of NO3- concentrations in ecosystems.

Temporal Variability of Stemflow Dissolved Organic Carbon (DOC) Concentrations and Quality from Morphologically Contrasting Deciduous Canopies

NASA Astrophysics Data System (ADS)

van Stan, J. T.; Levia, D. F.; Inamdar, S. P.; Mitchell, M. J.; Mage, S. M.

2010-12-01

Dissolved organic carbon (DOC) inputs from canopy-derived hydrologic fluxes play a significant role in the terrestrial carbon budgets of forested ecosystems. However, no studies known to the authors have examined the variability of both DOC concentrations and quality for stemflow across time scales, nor has any study to date evaluated the effects of canopy structure on stemflow DOC characteristics. This investigation seeks to rectify this knowledge gap by examining the variability of stemflow DOC concentrations and quality across contrasting canopy morphologies and time scales (seasonal, storm and intrastorm). Bulk and intrastorm stemflow samples from a less dense, rough-barked, more plagiophile (Liriodendron tulipifera L. (tulip poplar)) and a denser, thin-barked, more erectophile (Fagus grandifolia Ehrh. (American beech)) canopy were collected and analyzed for DOC quality using metrics derived from UV-vis spectroscopy (E2:E3 ratio, SUVA254, select spectral slope (S), and spectral slope ratios (SR)). Our results suggest that stemflow DOC concentrations and quality change as crown architectural traits enhance or diminish hydrologic retention time within the canopy. The architecture of L. tulipifera canopies likely retards the flow of intercepted water, increasing chemical exchange with bark and foliar surfaces. UV-vis metrics indicated that this increased chemical exchange, particularly with bark surfaces, generally enhanced aromatic hydrocarbon content and increased molecular weight. Because leaf presence influenced DOC quality, stemflow DOC characteristics also varied seasonally in response to canopy condition. At the inter- and intrastorm scale, stemflow DOC concentration and quality varied with meteorological and antecedent canopy conditions. Since recent studies have linked stemflow production to preferential subsurface transport of dissolved chemistries, trends in DOC speciation and fluxes described in this study may impact soil environments within wooded ecosystems.

The Influence of Submarine Groundwater Discharge on Nearshore Marine Dissolved Organic Carbon Reactivity, Concentration Dynamics, and Offshore Export

NASA Astrophysics Data System (ADS)

Goodridge, B.

2017-12-01

Dissolved organic carbon (DOC) is the largest pool of reduced carbon in the oceans, with a reservoir equivalent to atmospheric CO2. In nearshore marine regions, DOC sources include primary production, terrestrial DOC delivered by river discharge, and/or terrestrial and marine DOC delivered via submarine groundwater discharge (SGD). While the importance of SGD to coastal carbon cycling has been implicated, the actual influence of this process on nearshore carbon dynamics and offshore export has not been explicitly identified. This study, conducted at a predominantly marine-influenced intertidal beach-nearshore ocean system along the Santa Barbara, California coastline, aimed to address this knowledge gap. I coupled dark, temperature-controlled laboratory incubations, radioisotopic (Rn-222) SGD estimates, and a DOC box model to identify the influence of pore water mixing with seawater on nearshore DOC reactivity, concentration dynamics, and offshore export. Even with a relatively low volumetric contribution, SGD pore water mixing altered nearshore DOC reactivity, and elevated the nearshore DOC concentration by 0.9 to 5.6 µmol L-1 over nearshore seawater residence times ranging from 1 to 6 days. These elevated DOC concentrations were equivalent to 1.2 to 7.5% of the mean offshore DOC concentration taken during the summer months in the Santa Barbara Channel, when the coastal water column is highly thermally stratified. Despite the challenge of assessing carbon dynamics in physically and biogeochemically complex nearshore marine regions, this study demonstrates the need for future investigations to assess and account for SGD as a non-trivial component of coastal marine carbon cycles.

Sources and characteristics of organic matter in the Clackamas River, Oregon, related to the formation of disinfection by-products in treated drinking water

USGS Publications Warehouse

Carpenter, Kurt D.; Kraus, Tamara E.C.; Goldman, Jami H.; Saraceno, John Franco; Downing, Bryan D.; Bergamaschi, Brian A.; McGhee, Gordon; Triplett, Tracy

2013-01-01

This study characterized the amount and quality of organic matter in the Clackamas River, Oregon, to gain an understanding of sources that contribute to the formation of chlorinated and brominated disinfection by-products (DBPs), focusing on regulated DBPs in treated drinking water from two direct-filtration treatment plants that together serve approximately 100,000 customers. The central hypothesis guiding this study was that natural organic matter leaching out of the forested watershed, in-stream growth of benthic algae, and phytoplankton blooms in the reservoirs contribute different and varying proportions of organic carbon to the river. Differences in the amount and composition of carbon derived from each source affects the types and concentrations of DBP precursors entering the treatment plants and, as a result, yield varying DBP concentrations and species in finished water. The two classes of DBPs analyzed in this study-trihalomethanes (THMs) and haloacetic acids (HAAs)-form from precursors within the dissolved and particulate pools of organic matter present in source water. The five principal objectives of the study were to (1) describe the seasonal quantity and character of organic matter in the Clackamas River; (2) relate the amount and composition of organic matter to the formation of DBPs; (3) evaluate sources of DBP precursors in the watershed; (4) assess the use of optical measurements, including in-situ fluorescence, for estimating dissolved organic carbon (DOC) concentrations and DBP formation; and (5) assess the removal of DBP precursors during treatment by conducting treatability "jar-test" experiments at one of the treatment plants. Data collection consisted of (1) monthly sampling of source and finished water at two drinking-water treatment plants; (2) event-based sampling in the mainstem, tributaries, and North Fork Reservoir; and (3) in-situ continuous monitoring of fluorescent dissolved organic matter (FDOM), turbidity, chlorophyll-a, and other constituents to continuously track source-water conditions in near real-time. Treatability tests were conducted during the four event-based surveys to determine the effectiveness of coagulant and powdered activated carbon (PAC) on the removal of DBP precursors. Sample analyses included DOC, total particulate carbon (TPC), total and dissolved nutrients, absorbance and fluorescence spectroscopy, and, for regulated DBPs, concentrations of THMs and HAAs in finished water and laboratory-based THM and HAA formation potentials (THMFP and HAAFP, respectively) for source water and selected locations throughout the watershed. The results of this study may not be typical given the record and near record amounts of precipitation that occurred during spring that produced streamflow much higher than average in 2010-11. Although there were algal blooms, lower concentrations of chlorophyll-a were observed in the water column during the study period compared to historical data. Concentrations of DBPs in finished (treated) water averaged 0.024 milligrams per liter (mg/L) for THMs and 0.022 mg/L for HAAs; maximum values were about 0.040 mg/L for both classes of DBPs. Although DBP concentrations were somewhat higher within the distribution system, none of the samples collected for this study or for the quarterly compliance monitoring by the water utilities exceeded levels permissible under existing U.S. Environmental Protection Agency (USEPA) regulations: 0.080 mg/L for THMs and 0.060 mg/L for HAAs. DOC concentrations were generally low in the Clackamas River, typically about 1.0-1.5 mg/L. Concentrations in the mainstem occasionally increased to nearly 2.5 mg/L during storms; DOC concentrations in tributaries were sometimes much higher (up to 7.8 mg/L). The continuous in-situ FDOM measurements indicated sharp rises in DOC concentrations in the mainstem following rainfall events; concentrations were relatively stable during summer base flow. Even though the first autumn storm mobilized appreciable quantities of carbon, higher concentrations of DBPs in finished water were observed 3-weeks later, after the ground was saturated from additional rainfall. The majority of the DOC in the lower Clackamas River appears to originate from the upper basin, suggesting terrestrial carbon was commonly the dominant source. Lower-basin tributaries typically contained the highest concentrations of DOC and DBP precursors and contributed substantially to the overall loads in the mainstem during storms. During low-flow periods, tributaries were not major sources of DOC or DBP precursors to the Clackamas River. Although the dissolved fraction of organic carbon contributed the majority of DBP precursors, at times the particulate fraction (inorganic sediment and organic particles including detritus and algal material) contributed a substantial fraction of DBP precursors. Considering just the main-stem sites, on average, 10 percent of THMFP and 32 percent of HAAFP were attributed to particulate carbon. This finding suggests water-treatment methods that remove particles prior to chlorination would reduce finished-water DBP concentrations to some degree. Overall, concentrations of THM and HAA precursors were closely linked to DOC concentrations; laboratory DBP formation potentials (DBPFPs) clearly showed that THMFP and HAAFP were greatest in the downstream tributaries that contained elevated carbon concentrations. However, carbon-normalized "specific" formation potentials for THMs and HAAs (STHMFP and SHAAFP, respectively) revealed changes in carbon character over time that affected the two types of DBP classes differently. HAA precursors were elevated in waters containing aromatic-rich soil-derived material arising from forested areas. In contrast, THM precursors were associated with carbon having a lower aromatic content; highest STHMFP occurred in autumn 2011 in the mainstem from North Fork Reservoir downstream to LO DWTP. This pattern suggests the potential for a link between THM precursors and algal-derived carbon. The highest STHMFP value was measured within North Fork Reservoir, indicating reservoir derived carbon may be important for this class of DBPs. Weak correlations between STHMFP and SHAAFP emphasize that precursor sources for these types of DBPs may be different. This highlights not only that different locations within the watershed produce carbon with different reactivity (specific DBPFP), but also that different management approaches for each class of DBP precursors could be required for control. Treatability tests conducted on source water during four basin-wide surveys demonstrated that an average of about 40 percent of DOC can be removed by coagulation. While the decrease in THMFP following coagulation was similar to DOC, the decrease in HAAFP was much greater (approximately 70 percent), indicating coagulation is particularly effective at removing HAA precursors'likely because of the aromatic nature of the carbon associated with HAA precursors. Several findings from this study have direct implications for managing drinking-water resources and for providing useful information that may help improve treatment-plant operations. For example, the use of in-situ fluorometers that measure FDOM provided an excellent proxy for DOC concentration in this system and revealed short-term, rapid changes in DOC concentration during storm events. In addition, the strong correlation between FDOM values measured in-situ and HAA5 concentrations in finished water may permit estimation of continuous HAA concentrations, as was done here. As part of this study, multiple in-situ FDOM sensors were deployed continuously and in real-time to characterize the composition of dissolved organic matter. Although the initial results were promising, additional research and engineering developments will be needed to demonstrate the full utility of these sensors for this purpose. In conclusion, although DBPFPs were strongly correlated to DOC concentration, some DBPs formed from particulate carbon, including terrestrial leaf material and algal material such as planktonic species of blue-green algae and sloughed filaments, stalks, and cells of benthic algae. Different precursor sources in the watershed were evident from the data, suggesting specific actions may be available to address some of these sources. In-situ measurements of FDOM proved to be an excellent proxy for DOC concentration as well as HAA formation during treatment, which suggests further development and refinement of these sensors have the potential to provide real-time information about complex watershed processes to operators at the drinking-water treatment plants. Follow-up studies could examine the relative roles that terrestrial and algal sources have on the DBP precursor pool to better understand how watershed-management activities may be affecting the transport of these compounds to Clackamas River drinking-water intakes. Given the low concentrations of algae in the water column during this study, additional surveys during more typical river conditions could provide a more complete understanding of how algae contribute DBP precursors. Further development of FDOM-sensor technology can improve our understanding of carbon dynamics in the river and how concentrations may be trending over time. This study was conducted in collaboration with Clackamas River Water and the City of Lake Oswego water utilities. Other research partners included Oregon Health and Science University in Hillsboro, Oregon, Alexin Laboratory in Tigard, Oregon, U.S. Geological Survey National Research Program Laboratory in Denver, Colorado, and the U.S. Geological Survey Water Science Centers in Portland, Oregon, and Sacramento, California. This project was supported with funding from Clackamas River Water, City of Lake Oswego, the U.S. Geological Survey, and the Water Research Foundation.

Humic substances-part 7: the biogeochemistry of dissolved organic carbon and its interactions with climate change.

PubMed

Porcal, Petr; Koprivnjak, Jean-François; Molot, Lewis A; Dillon, Peter J

2009-09-01

Dissolved organic matter, measured as dissolved organic carbon (DOC), is an important component of aquatic ecosystems and of the global carbon cycle. It is known that changes in DOC quality and quantity are likely to have ecological repercussions. This review has four goals: (1) to discuss potential mechanisms responsible for recent changes in aquatic DOC concentrations; (2) to provide a comprehensive overview of the interactions between DOC, nutrients, and trace metals in mainly boreal environments; (3) to explore the impact of climate change on DOC and the subsequent effects on nutrients and trace metals; and (4) to explore the potential impact of DOC cycling on climate change. We review recent research on the mechanisms responsible for recent changes in aquatic DOC concentrations, DOC interactions with trace metals, N, and P, and on the possible impacts of climate change on DOC in mainly boreal lakes. We then speculate on how climate change may affect DOC export and in-lake processing and how these changes might alter nutrient and metal export and processing. Furthermore, the potential impacts of changing DOC cycling patterns on climate change are examined. It has been noted that DOC concentrations in lake and stream waters have increased during the last 30 years across much of Europe and North America. The potential reasons for this increase include increasing atmospheric CO(2) concentration, climate warming, continued N deposition, decreased sulfate deposition, and hydrological changes due to increased precipitation, droughts, and land use changes. Any change in DOC concentrations and properties in lakes and streams will also impact the acid-base chemistry of these waters and, presumably, the biological, chemical, and photochemical reactions taking place. For example, the interaction of trace metals with DOC may be significantly altered by climate change as organically complexed metals such as Cu, Fe, and Al are released during photo-oxidation of DOC. The production and loss of DOC as CO(2) from boreal lakes may also be affected by changing climate. Climate change is unlikely to be uniform spatially with some regions becoming wetter while others become drier. As a result, rates of change in DOC export and concentrations will vary regionally and the changes may be non-linear. Climate change models predict that higher temperatures are likely to occur over most of the boreal forests in North America, Europe, and Asia over the next century. Climate change is also expected to affect the severity and frequency of storm and drought events. Two general climate scenarios emerge with which to examine possible DOC trends: warmer and wetter or warmer and drier. Increasing temperature and hydrological changes (specifically, runoff) are likely to lead to changes in the quality and quantity of DOC export from terrestrial sources to rivers and lakes as well as changes in DOC processing rates in lakes. This will alter the quality and concentrations of DOC and its constituents as well as its interactions with trace metals and the availability of nutrients. In addition, export rates of nutrients and metals will also change in response to changing runoff. Processing of DOC within lakes may impact climate depending on the extent to which DOC is mineralized to dissolved inorganic carbon (DIC) and evaded to the atmosphere or settles as particulate organic carbon (POC) to bottom sediments and thereby remaining in the lake. The partitioning of DOC between sediments and the atmosphere is a function of pH. Decreased DOC concentrations may also limit the burial of sulfate, as FeS, in lake sediments, thereby contributing acidity to the water by increasing the formation of H(2)S. Under a warmer and drier scenario, if lake water levels fall, previously stored organic sediments may be exposed to greater aeration which would lead to greater CO(2) evasion to the atmosphere. The interaction of trace metals with DOC may be significantly altered by climate change. Iron enhances the formation of POC during irradiation of lake water with UV light and therefore may be an important pathway for transfer of allochthonous DOC to the sediments. Therefore, changing Fe/DOC ratios could affect POC formation rates. If climate change results in altered DOC chemistry (e.g., fewer and/or weaker binding sites) more trace metals could be present in their toxic and bioavailable forms. The availability of nutrients may be significantly altered by climate change. Decreased DOC concentrations in lakes may result in increased Fe colloid formation and co-incident loss of adsorbable P from the water column. Climate change expressed as changes in runoff and temperature will likely result in changes in aquatic DOC quality and concentration with concomitant effects on trace metals and nutrients. Changes in the quality and concentration of DOC have implications for acid-base chemistry and for the speciation and bioavailability of certain trace metals and nutrients. Moreover, changes in DOC, metals, and nutrients are likely to drive changes in rates of C evasion and storage in lake sediments. The key controls on allochthonous DOC quality, quantity, and catchment export in response to climate change are still not fully understood. More detailed knowledge of these processes is required so that changes in DOC and its interactions with nutrients and trace metals can be better predicted based on changes caused by changing climate. More studies are needed concerning the effects of trace metals on DOC, the effects of changing DOC quality and quantity on trace metals and nutrients, and how runoff and temperature-related changes in DOC export affect metal and nutrient export to rivers and lakes.

Local and regional scale exchanges of dissolved organic carbon (DOC) between tidal wetlands and their adjacent coastal waters

NASA Astrophysics Data System (ADS)

Osburn, C. L.; Joshi, I.; Lebrasse, M. C.; Oviedo-Vargas, D.; Bianchi, T. S.; Bohnenstiehl, D. R.; D'Sa, E. J.; He, R.; Ko, D.; Arellano, A.; Ward, N. D.

2017-12-01

The contribution of blue carbon from tidal wetlands to the coastal ocean in the form of dissolved organic carbon (DOC) represents a terrestrial-aquatic linkage of increasing importance. DOC flux results will be presented from local (tidal creek) and regional (bays) scale studies in which various combinations of field observations, ocean-color satellite observations, and the outputs of high-resolution hydrodynamic models were used to estimate DOC export. The first project was located in Bald Head Creek, a tributary to the Cape Fear River estuary in eastern North Carolina (NC). DOC fluxes were computed using a bathymetric data collected via unmanned surface vehicle (USV) and a numerical hydrodynamic model (SCHISM) based on the relationships between colored dissolved organic matter (CDOM) absorption, DOC concentration, and salinity taken from field observations. Model predictions estimated an annual net export of DOC at 54 g C m-2 yr-1 from the tidal creek to the adjacent estuary. Carbon stable isotope (δ13C) values were used to estimate the contribution of wetland carbon to this export. In the second project, DOC fluxes from the Apalachicola Bay, FL, Barataria Bay, LA, were based on the development of algorithms between DOC and CDOM absorption derived from the VIIRS ocean color sensor. The Navy Coastal Ocean Model (NCOM) was used to compute salt flux estimates from each bay to the Louisiana-Texas shelf. The relationship between salinity and CDOM was used to estimate net annual DOC exports of 8.35 x 106 g C m-2 y-1 (Apalachicola Bay) and 7.14 x 106 g C m-2 yr-1 (Barataria Bay). These values approximate 13% and 9% of the annual loads of DOC from the Mississippi River to the Gulf of Mexico, respectively. CDOM and lignin were used in a mixing model to estimate wetland-derived DOC were 2% for Apalachicola Bay and 13% for Barataria Bay, the latter having one of the highest rates of relative sea level rise in North America. Results from our project demonstrated the utility of CDOM, amenable to high resolution observations from multiple platforms, as a basis for constraining the heterogeneity of DOC exports from tidal wetlands to estuaries and coastal waters using numerical models at local and regional scales.

The Spatial and Temporal Distribution of Dissolved Organic Carbon Exported from Three Chinese Rivers to the China Sea

PubMed Central

Shi, Guohua; Peng, Changhui; Wang, Meng; Shi, Shengwei; Yang, Yanzheng; Chu, Junyao; Zhang, Junjun; Lin, Guanghui; Shen, Yan; Zhu, Qiuan

2016-01-01

The lateral transport of dissolved organic carbon (DOC) plays an important role in linking the carbon cycles of terrestrial and aquatic ecosystems. Neglecting the lateral flow of dissolved organic carbon can lead to an underestimation of the organic carbon budget of terrestrial ecosystems. It is thus necessary to integrate DOC concentrations and flux into carbon cycle models, particularly with regard to the development of models that are intended to directly link terrestrial and ocean carbon cycles. However, to achieve this goal, more accurate information is needed to better understand and predict DOC dynamics. In this study, we compiled an inclusive database of available data collected from the Yangtze River, Yellow River and Pearl River in China. The database is collected based on online literature survey and analysed by statistic method. Overall, our results revealed a positive correlation between DOC flux and discharge in all three rivers, whereas the DOC concentration was more strongly correlated with the regional net primary productivity (NPP). We estimated the total DOC flux exported by the three rivers into the China Sea to be approximately 2.73 Tg yr-1. Specifically, the annual flux of DOC from the Yangtze River, Yellow River and Pearl River was estimated to be 1.85 Tg yr-1, 0.06 Tg yr-1 and 0.82 Tg yr-1, respectively, and the average annual DOC concentrations were estimated to be 2.24 ± 0.53 mg L-1, 2.70 ± 0.38 mg L-1 and 1.51 ± 0.09 mg L-1, respectively. Seasonal variations in DOC concentrations are greatly influenced by the interaction between temperature and precipitation. NPP is significantly and positively related to the DOC concentration in the Yangtze River and the Pearl River. In addition, differences in climate and the productivity of the vegetation may influence both the flux and concentrations of DOC transported by the rivers and thus potentially affect estuarine geochemistry. PMID:27755581

Soil-solution partitioning of DOC in acid organic soils: Results from a UK field acidification and alkalization experiment

NASA Astrophysics Data System (ADS)

Oulehle, Filip; Jones, Timothy; Burden, Annette; Evans, Chris

2013-04-01

Dissolved organic carbon (DOC) is an important component of the global carbon (C) cycle and has profound impacts on water chemistry and metabolism in lakes and rivers. Reported increases of DOC concentration in surface waters across Europe and Northern America have been attributed to several drivers; from changing climate and land-use to eutrophication and declining acid deposition. The last of these suggests that acidic deposition suppressed the solubility of DOC, and that this historic suppression is now being reversed by reducing emissions of acidifying pollutants. We studied a set of four parallel acidification and alkalization experiments in organic rich soils which, after three years of manipulation, have shown clear soil solution DOC responses to acidity change. We tested whether these DOC concentration changes were related to changes in the acid/base properties of DOC. Based on laboratory determination of DOC site density (S.D. = amount of carboxylic groups per milligram DOC) and charge density (C.D. = organic acid anion concentration per milligram DOC) we found that the change in DOC soil-solution partitioning was tightly related to the change in degree of dissociation (α = C.D./S.D. ratio) of organic acids (R2=0.74, p<0.01). Carbon turnover in soil organic matter (SOM), determined by soil respiration and β-D-glucosidase enzyme activity measurements, also appears to have some impact on DOC leaching, via constraints on the actual supply of available DOC from SOM; when the turnover rate of C in SOM is low, the effect of α on DOC leaching is reduced. Thus, differences in the magnitude of DOC changes seen across different environments might be explained by interactions between physicochemical restrictions of DOC soil-solution partitioning, and SOM carbon turnover effects on DOC supply.

Coupled mobilization of dissolved organic matter and metals (Cu and Zn) in soil columns

NASA Astrophysics Data System (ADS)

Zhao, Lu Y. L.; Schulin, Rainer; Weng, Liping; Nowack, Bernd

2007-07-01

Dissolved organic carbon (DOC) is a key component involved in metal displacement in soils. In this study, we investigated the concentration profiles of soil-borne DOC, Cu and Zn at various irrigation rates with synthetic rain water under quasi steady-state conditions, using repacked soil columns with a metal-polluted topsoil and two unpolluted subsoils. Soil solution was collected using suction cups installed at centimeter intervals over depth. In the topsoil the concentrations of DOC, dissolved metals (Zn and Cu), major cations (Ca 2+ and Mg 2+) and anions ( NO3- and SO42-) increased with depth. In the subsoil, the Cu and Zn concentrations dropped to background levels within 2 cm. All compounds were much faster mobilized in the first 4 cm than in the rest of the topsoil. DOC and Cu concentrations were higher at higher flow rates for a given depth, whereas the concentrations of the other ions decreased with increasing flow rate. The decomposition of soil organic matter resulted in the formation of DOC, SO42-, and NO3- and was the main driver of the system. Regression analysis indicated that Cu mobilization was governed by DOC, whereas Zn mobilization was primarily determined by Ca and to a lesser extent by DOC. Labile Zn and Cu 2+ concentrations were well predicted by the NICA-Donnan model. The results highlight the value of high-resolution in-situ measurements of DOC and metal mobilization in soil profiles.

Degradation potentials of dissolved organic carbon (DOC) from thawed permafrost peat

PubMed Central

Panneer Selvam, Balathandayuthabani; Lapierre, Jean-François; Guillemette, Francois; Voigt, Carolina; Lamprecht, Richard E.; Biasi, Christina; Christensen, Torben R.; Martikainen, Pertti J.; Berggren, Martin

2017-01-01

Global warming can substantially affect the export of dissolved organic carbon (DOC) from peat-permafrost to aquatic systems. The direct degradability of such peat-derived DOC, however, is poorly constrained because previous permafrost thaw studies have mainly addressed mineral soil catchments or DOC pools that have already been processed in surface waters. We incubated peat cores from a palsa mire to compare an active layer and an experimentally thawed permafrost layer with regard to DOC composition and degradation potentials of pore water DOC. Our results show that DOC from the thawed permafrost layer had high initial degradation potentials compared with DOC from the active layer. In fact, the DOC that showed the highest bio- and photo-degradability, respectively, originated in the thawed permafrost layer. Our study sheds new light on the DOC composition of peat-permafrost directly upon thaw and suggests that past estimates of carbon-dioxide emissions from thawed peat permafrost may be biased as they have overlooked the initial mineralization potential of the exported DOC. PMID:28378792

Diel fluctuations of viscosity-driven riparian inflow affect streamflow DOC concentration

NASA Astrophysics Data System (ADS)

Schwab, Michael P.; Klaus, Julian; Pfister, Laurent; Weiler, Markus

2018-04-01

Diel fluctuations of stream water DOC concentrations are generally explained by a complex interplay of different instream processes. We measured the light absorption spectrum of water and DOC concentrations in situ and with high frequency by means of a UV-Vis spectrometer during 18 months at the outlet of a forested headwater catchment in Luxembourg (0.45 km2). We generally observed diel DOC fluctuations with a maximum in the afternoon during days that were not affected by rainfall-runoff events. We identified an increased inflow of terrestrial DOC to the stream in the afternoon, causing the DOC maxima in the stream. The terrestrial origin of the DOC was derived from the SUVA-254 (specific UV absorbance at 254 nm) index, which is a good indicator for the aromaticity of DOC. In the studied catchment, the most likely process that can explain the diel DOC input variations towards the stream is the so-called viscosity effect. The water temperature in the upper parts of the saturated riparian zone is increasing during the day, leading to a lower viscosity and therefore a higher hydraulic conductivity. Consequently, more water from areas that are rich in terrestrial DOC passes through the saturated riparian zone and contributes to streamflow in the afternoon. We believe that not only diel instream processes, but also viscosity-driven diel fluctuations of terrestrial DOC input should be considered to explain diel DOC patterns in streams.

Variation of dissolved organic carbon transported by two Chinese rivers: The Changjiang River and Yellow River.

PubMed

Liu, Dong; Pan, Delu; Bai, Yan; He, Xianqiang; Wang, Difeng; Zhang, Lin

2015-11-15

Real-time monitoring of riverine dissolved organic carbon (DOC) and the associated controlling factors is essential to coastal ocean management. This study was the first to simulate the monthly DOC concentrations at the Datong Hydrometric Station for the Changjiang River and at the Lijin Hydrometric Station for the Yellow River from 2000 to 2013 using a multilayer back-propagation neural network (MBPNN), along with basin remote-sensing products and river in situ data. The average absolute error between the modeled values and in situ values was 9.98% for the Changjiang River and 10.84% for the Yellow River. As an effect of water dilution, the variations of DOC concentrations in the two rivers were significantly negatively affected by discharge, with lower values reported during the wet season. Moreover, vegetation growth status and agricultural activities, represented by the gross primary product (GPP) and cropland area percent (CropPer) in the river basin, respectively, also significantly affected the DOC concentration in the Changjiang River, but not the Yellow River. The monthly riverine DOC flux was calculated using modeled DOC concentrations. In particular, the riverine DOC fluxes were affected by discharge, with 71.06% being reported for the Changjiang River and 90.71% for the Yellow River. Over the past decade, both DOC concentration and flux in the two rivers have not shown significant changes. Copyright © 2015 Elsevier Ltd. All rights reserved.

Photochemical influences on the air-water exchange of mercury

NASA Astrophysics Data System (ADS)

Vette, Alan Frederic

The formation of dissolved gaseous mercury (DGM) in natural waters is an important component in the biogeochemical cycle of mercury (Hg). The predominate form of DGM in natural waters, gaseous elemental Hg (Hg0), may be transferred from the water to the atmosphere. Gas exchange may reduce the amount of Hg available for methyl-Hg formation, the most toxic form of Hg that bioaccumulates in the food chain. Determining the mechanisms and rates of DGM formation is essential in understanding the fate and cycling of Hg in aquatic ecosystems. Field and laboratory experiments were conducted to evaluate the effect of light on DGM formation in surface waters containing different levels of dissolved organic carbon (DOC). Water samples collected from the Tahqwamenon River and Whitefish Bay on Lake Superior were amended with divalent Hg (Hg2+) and irradiated under a variety of reaction conditions to determine rates of DGM formation. The water samples were also analyzed for various Hg species (total, filtered, easily reducible and dissolved gaseous Hg), DOC and light attenuation. Additional field studies were conducted on Lake Michigan to measure gaseous Hg in air and water. These data were used to develop a mechanistic model to estimate air-water exchange of gaseous Hg. This research found that photochemical formation of DGM was affected by penetration of UV A radiation (320-400 nm). Formation of DGM was enhanced at higher DOC concentrations, indicating DOC photosensitized the reduction of Hg2+ to Hg0. Wavelength studies determined that formation of DGM was significantly reduced in the absence of UV A. Field studies showed DGM concentrations were highest near the water surface and peaked at mid-day, indicating a photo-induced source of DGM. The conversion of reducible Hg2+ to Hg0 was suppressed in high DOC waters where UV A penetration was limited. The mechanistic model predicted similar DGM concentrations to the observed values and demonstrated that deposition and emission fluxes of gaseous Hg were similar in Lake Michigan. In addition, deposition and emission fluxes of gaseous Hg were similar to Hg loadings by precipitation. The formation and emission of DGM from surface waters represents a significant contribution to the Hg cycle in aquatic ecosystems.

Influence of allochthonous dissolved organic matter on pelagic basal production in a northerly estuary

NASA Astrophysics Data System (ADS)

Andersson, A.; Brugel, S.; Paczkowska, J.; Rowe, O. F.; Figueroa, D.; Kratzer, S.; Legrand, C.

2018-05-01

Phytoplankton and heterotrophic bacteria are key groups at the base of aquatic food webs. In estuaries receiving riverine water with a high content of coloured allochthonous dissolved organic matter (ADOM), phytoplankton primary production may be reduced, while bacterial production is favoured. We tested this hypothesis by performing a field study in a northerly estuary receiving nutrient-poor, ADOM-rich riverine water, and analyzing results using multivariate statistics. Throughout the productive season, and especially during the spring river flush, the production and growth rate of heterotrophic bacteria were stimulated by the riverine inflow of dissolved organic carbon (DOC). In contrast, primary production and photosynthetic efficiency (i.e. phytoplankton growth rate) were negatively affected by DOC. Primary production related positively to phosphorus, which is the limiting nutrient in the area. In the upper estuary where DOC concentrations were the highest, the heterotrophic bacterial production constituted almost 100% of the basal production (sum of primary and bacterial production) during spring, while during summer the primary and bacterial production were approximately equal. Our study shows that riverine DOC had a strong negative influence on coastal phytoplankton production, likely due to light attenuation. On the other hand DOC showed a positive influence on bacterial production since it represents a supplementary food source. Thus, in boreal regions where climate change will cause increased river inflow to coastal waters, the balance between phytoplankton and bacterial production is likely to be changed, favouring bacteria. The pelagic food web structure and overall productivity will in turn be altered.

Effects of elevated sulfate concentration on the mobility of arsenic in the sediment-water interface.

PubMed

Li, Shiyu; Yang, Changliang; Peng, Changhui; Li, Haixia; Liu, Bin; Chen, Chuan; Chen, Bingyu; Bai, Jinyue; Lin, Chen

2018-06-15

The adsorption/desorption of arsenic (As) at the sediment-water interface in lakes is the key to understanding whether As can enter the ecosystem and participate in material circulation. In this study, the concentrations of As(III), total arsenic [As(T)], sulfide, iron (Fe), and dissolved organic carbon (DOC) in overlying water were observed after the initial sulfate (SO 4 2- ) concentrations were increased by four gradients in the presence and absence of microbial systems. The results indicate that increased SO 4 2- concentrations in overlying water triggered As desorption from sediments. Approximately 10% of the desorbed As was desorbed directly as arsenite or arsenate by competitive adsorption sites on the iron salt surface; 21% was due to the reduction of iron (hydr)oxides; and 69% was due to microbial activity, as compared with a system with no microbial activity. The intensity of microbial activity was controlled by the SO 4 2- and DOC concentrations in the overlying water. In anaerobic systems, which had SO 4 2- and DOC concentrations higher than 47 and 7 mg/L, respectively, microbial activity was promoted by SO 4 2- and DOC; As(III) was desorbed under these indoor simulation conditions. When either the SO 4 2- or DOC concentration was lower than its respective threshold of 47 or 7 mg/L, or when either of these indices was below its concentration limit, it was difficult for microorganisms to use SO 4 2- and DOC to enhance their own activities. Therefore, conditions were insufficient for As desorption. The migration of As in lake sediments was dominated by microbial activity, which was co-limited by SO 4 2- and DOC. The concentrations of SO 4 2- and DOC in the overlying water are thus important for the prevention and control of As pollution in lakes. We recommend controlling SO 4 2- and DOC concentrations as a method for controlling As inner-source pollution in lake water. Copyright © 2018 Elsevier Inc. All rights reserved.

Impact of managed moorland burning on DOC concentrations in soil solutions and stream waters

NASA Astrophysics Data System (ADS)

Palmer, Sheila; Wearing, Catherine; Johnson, Kerrylyn; Holden, Joseph; Brown, Lee

2013-04-01

In the UK uplands, prescribed burning of moorland vegetation is a common practice to maintain suitable habitats for game birds. Many of these landscapes are in catchments covered by significant deposits of blanket peat (typically one metre or more in depth). There is growing interest in the effect of land management on the stability of these peatland carbon stores, and their contribution to dissolved and particulate organic carbon in surface waters (DOC and POC, respectively) and subsequent effects on stream biogeochemistry and ecology. Yet there are surprisingly few published catchment-scale studies on the effect of moorland burning on DOC and POC. As part of the EMBER project, stream chemistry data were collected approximately monthly in ten upland blanket peat catchments in the UK, five of which acted as controls and were not subject to burning. The other five catchments were subject to a history of prescribed burning, typically in small patches (300-900 m2) in rotations of 8-25 years. Soil solution DOC was also monitored at four depths at two intensively studied sites (one regularly burned and one control). At the two intensive sites, soil solution DOC was considerably higher at the burned site, particularly in surface solutions where concentrations in excess of 100 mg/L were recorded on several occasions (median 37 mg/L over 18 months). The high soil solution DOC concentrations at the burned site occurred in the most recently burned plots (less than 2 years prior to start of sampling) and the lowest DOC concentrations were observed in plots burned 15-25 years previously. On average, median stream DOC and POC concentrations were approximately 43% and 35% higher respectively in burned catchments relative to control catchments. All streams exhibited peak DOC in late summer/early autumn with higher peak DOC concentrations in burned catchments (20-66 mg/L) compared to control catchments (18-54 mg/L). During winter months, DOC concentrations were low in control catchments (typically less than 15 mg/L) but were highly variable in burned catchments (9-40 mg/L), implying some instability of peat carbon stores and/or fluctuation in source. The results offer strong evidence for an impact of burning on the delivery of DOC to streams, possibly through increased surface run-off from bare or partially vegetated patches.

Identifying dissolved organic carbon sources at a gaged headwater catchment using FDOM sensors

NASA Astrophysics Data System (ADS)

Malzone, J. M.; Shanley, J. B.

2014-12-01

The United States Geological Survey's (USGS) W-9 gage at the headwaters of Sleepers River, Vermont has been monitored for dissolved organic carbon (DOC) concentration for more than 20 years. However, the sources of this DOC during base flow and hydrologic events remain unclear. The major objectives of this research were to identify sources of DOC during storm events and to explain the observed DOC-streamflow counterclockwise hysteresis during hydrologic events. Two main hypotheses to explain hysteresis during hydrologic events were tested: (1) distant headwater wetlands are the major DOC source, which lags behind peak flow due to travel time; and (2) the entire watershed contributes to the DOC at the gage, but the response of DOC lags behind the period when groundwater contributes most to streamflow. Sources of DOC were tracked using fluorescent dissolved organic matter (FDOM) sensors in surface water and groundwater wells. Wells were installed at four depths, 0.3, 0.6, 0.9, and 1.2 m, at four sites: a peaty low-gradient riparian area near the headwaters; a mid-hillslope area on a long hillslope mid-watershed; a near-stream area on a long hillslope mid-watershed; and a low-gradient tributary confluence area just above the gage. During storm events, FDOM and hydraulic head were measured at the nested groundwater wells. Samples for DOC analysis were also taken to determine the relationship between FDOM and DOC. Results suggest that both distant sources and the greater watershed played a role in the transport of DOC to the W-9 gage. Distant peaty sources dominated during large storms and contributed the highest surface water FDOM measurements. The peak FDOM at the gage was therefore best described as a result of transport. However, export from these distant sources terminated rapidly and did not explain continued elevated FDOM at the gage. Groundwater across the watershed exhibited hysteresis analogous to that in the stream itself, with FDOM peaking as head receded. As groundwater is recharged, the water table intersects more carbon rich soil layers. Pre-event water is flushed out first before event water mobilizes DOC, causing the groundwater hysteresis. High FDOM groundwater discharging to the stream likely sustained elevated FDOM at the gage. The gage hysteresis, therefore, seems to be a result of both hypotheses tested.

[Effects of nitrogen deposition on the concentration and spectral characteristics of dissolved organic matter in soil solution in a young Cunninghamia lanceolata plantation.

PubMed

Yuan, Xiao Chun; Chen, Yue Min; Yuan, Shuo; Zheng, Wei; Si, You Tao; Yuan, Zhi Peng; Lin, Wei Sheng; Yang, Yu Sheng

2017-01-01

To study the effects of nitrogen deposition on the concentration and spectral characteristics of dissolved organic matter (DOM) in the forest soil solution from the subtropical Cunninghamia lanceolata plantation, using negative pressure sampling method, the dynamics of DOM in soil solutions from 0-15 and 15-30 cm soil layer was monitored for two years and the spectroscopic features of DOM were analyzed. The results showed that nitrogen deposition significantly reduced the concentration of dissolved organic carbon (DOC), and increased the aromatic index (AI) and the humic index (HIX), but had no significant effect on dissolved organic nitrogen (DON) concentration in both soil layers. There was obvious seasonal variation in DOM concentration of the soil solution, which was prominently higher in summer and autumn than in spring and winter.Fourier-transform infrared (FTIR) absorption spectrometry indicated that the DOM in forest soil solution had absorption peaks in the similar position of six regions, being the highest in wave number of 1145-1149 cm -1 . Three-dimensional fluorescence spectra indicated that DOM was mainly consisted of protein-like substances (Ex/Em=230 nm/300 nm) and microbial degradation products (Ex/Em=275 nm/300 nm). The availability of protein-like substances from 0-15 cm soil layer was reduced in the nitrogen treatments. Nitrogen deposition significantly reduced the concentration of DOC in soil solution, maybe largely by reducing soil pH, inhibiting soil carbon mineralization and stimulating plant growth. In particular, the decline of DOC concentration in the surface layer was due to the production inhibition of the protein-like substances and carboxylic acids. Short-term nitrogen deposition might be beneficial to the maintenance of soil fertility, while the long-term accumulation of nitrogen deposition might lead to the hard utilization of soil nutrients.

Dissolved organic carbon dynamics in a near-pristine boreal mire-forest-river landscape during spring snowmelt, Komi Republic, Russia

NASA Astrophysics Data System (ADS)

Avagyan, A.; Runkle, B.; Kutzbach, L.

2011-12-01

It is well known that peatlands represent an important soil carbon reserve. Therefore, they are considered as hot-spots with respect to climate change. However, lack of information concerning the transport of dissolved organic matter within peatlands and its release into fluvial systems represents a major gap in our understanding of both local and global carbon cycles. In particular, the spring snowmelt period, as a major hydrological event in the annual water cycle of boreal regions, strongly influences the fluxes of carbon between terrestrial and fluvial systems. The aim of this study is to provide thorough quantitative analyses of dissolved organic carbon (DOC) concentrations and fluxes in a boreal mire-forest-river landscape during the snowmelt period. Water samples were collected in the Komi Republic, Russia, in spring 2011 along transects across the near-pristine Ust-Pojeg mire complex and the nearby river Pojeg into which it drains (61°56'N, 50°13'E). This peatland is in a transitional state from fen to bog and consists of minerogeous, ombrogenous, and transitional forest-mire (lagg) zones. Microtopographic features include hummocks, hollows, and lawns. High frequency absorption measurements were conducted directly at the study site with a portable UV-Vis spectrometer over a wavelength range of 200-742.5 nm at 2.5 nm intervals. These results were calibrated against values obtained from the catalytically-aided platinum 680°C combustion technique. The results showed that in the beginning of the snowmelt period only surface carbon is flushed away by melted snow water while deeper layers remain frozen. During this time, DOC concentrations fluctuated within the range of 10-14 mg L-1 across the whole mire complex. During the later stages of snowmelt, concentrations of DOC were different between lagg, fen and bog zones, which separated them into distinct hydrological and biogeochemical units within the mire complex. The highest concentration was observed at the lagg zone with 30 mg L-1, while the lowest concentration was found at the bog site 15 mg L-1. The river water DOC concentration reached about 25 mg L-1 and was thus significantly increased compared to summer values of about 4.7 mg L-1. Water from the mire complex with a high DOC concentration was discharged via an outflow creek, into the river Pojeg. During the first flush during the snowmelt, the DOC concentration was approximately 60 mg L-1 in the outflow creek; after 10 days it decreased to 30-34 mg L-1. Additionally, we found that the following metals were discharged from the mire complex into the river as demonstrated by their concentrations in the outflow water: iron (0.34 mg L-1); manganese (28 μg L-1); arsenic (0.42 μg L-1); and mercury (0.020 μg L-1). These findings imply that the snowmelt water fluxes redistribute major parts of the carbon stock between the site's terrestrial and fluvial systems and affect the transport of metals. These large peatland regions could therefore play a substantial role as a carbon source for the river-ocean matter transport system.

Impact of wetland decline on decreasing dissolved organic carbon concentrations along the Mississippi River continuum

DOE Office of Scientific and Technical Information (OSTI.GOV)

Duan, Shuiwang; He, Yuxiang; Kaushal, Sujay S.

Prior to discharging to the ocean, large rivers constantly receive inputs of dissolved organic carbon (DOC) from tributaries or fringing floodplains and lose DOC via continuous in situ processing along distances that span thousands of kilometers. Current concepts predicting longitudinal changes in DOC mainly focus on in situ processing or exchange with fringing floodplain wetlands, while effects of heterogeneous watershed characteristics are generally ignored. We analyzed results from a 17-year time-series of DOC measurements made at seven sites and three expeditions along the entire Mississippi River main channel with DOC measurements made every 17 km. The results show a clearmore » downstream decrease in DOC concentrations that was consistent throughout the entire study period. Downstream DOC decreases were primarily (~63–71%) a result of constant dilutions by low-DOC tributary water controlled by watershed wetland distribution, while in situ processing played a secondary role. We estimate that from 1780 to 1980 wetland loss due to land-use alterations caused a ca. 58% decrease in in DOC concentrations in the tributaries of the Mississippi River. DOC reductions caused by watershed wetland loss likely impacted the capacity for the river to effectively remove nitrogen via denitrification, which can further exacerbate coastal hypoxia. Lastly, these findings highlight the importance of watershed wetlands in regulating DOC longitudinally along the headland to ocean continuum of major rivers.« less

Impact of wetland decline on decreasing dissolved organic carbon concentrations along the Mississippi River continuum

DOE PAGES

Duan, Shuiwang; He, Yuxiang; Kaushal, Sujay S.; ...

2017-01-09

Prior to discharging to the ocean, large rivers constantly receive inputs of dissolved organic carbon (DOC) from tributaries or fringing floodplains and lose DOC via continuous in situ processing along distances that span thousands of kilometers. Current concepts predicting longitudinal changes in DOC mainly focus on in situ processing or exchange with fringing floodplain wetlands, while effects of heterogeneous watershed characteristics are generally ignored. We analyzed results from a 17-year time-series of DOC measurements made at seven sites and three expeditions along the entire Mississippi River main channel with DOC measurements made every 17 km. The results show a clearmore » downstream decrease in DOC concentrations that was consistent throughout the entire study period. Downstream DOC decreases were primarily (~63–71%) a result of constant dilutions by low-DOC tributary water controlled by watershed wetland distribution, while in situ processing played a secondary role. We estimate that from 1780 to 1980 wetland loss due to land-use alterations caused a ca. 58% decrease in in DOC concentrations in the tributaries of the Mississippi River. DOC reductions caused by watershed wetland loss likely impacted the capacity for the river to effectively remove nitrogen via denitrification, which can further exacerbate coastal hypoxia. Lastly, these findings highlight the importance of watershed wetlands in regulating DOC longitudinally along the headland to ocean continuum of major rivers.« less

Determination of an organic-acid analog of DOC for use in copper toxicity studies on salmonids

DOE Office of Scientific and Technical Information (OSTI.GOV)

MacRae, R.K.; Meyer, J.S.; Hansen, J.A.

1995-12-31

Concentrations of dissolved copper in streams draining mine sites often exceed concentrations shown to cause acute and chronic mortality in salmonids. However, toxicity and impaired behaviors may be modified by dissolved organic carbon (DOC) and other inorganic components present in the site water. The effects of DOC on copper speciation, and thus bioavailability and toxicity, were determined by titrating stream waters with copper, using a cupric ion-specific electrode to detect free copper concentrations. Effects of various competing cations (e.g., Ca{sup +2}, Co{sup +2}) on copper-DOC binding were also evaluated. Titration results were evaluated using Scatchard and non-linear regression analyses tomore » quantify the strength and capacity of copper-DOC binding. Inorganic speciation was determined using the geochemical model MINEQL{sup +}. Results of these titrations indicated the presence of two or three distinct copper binding components in site water DOC. Three commercially available organic acids where then chosen to mimic the binding characteristics of natural DOC. This DOC-analog was used successfully in fish toxicity studies to evaluate the influence of DOC on copper bioavailability. Geochemical models were developed to predict copper speciation in both laboratory test waters and site waters, for any typical combination of water chemistry parameters (pH, alkalinity, [DOC], etc.). A combined interpretation of fish toxicity and modeling results indicate that some DOC-bound copper was bioavailable.« less

The conservative behavior of dissolved organic carbon in surface waters of the southern Chukchi Sea, Arctic Ocean, during early summer

PubMed Central

Tanaka, Kazuki; Takesue, Nobuyuki; Nishioka, Jun; Kondo, Yoshiko; Ooki, Atsushi; Kuma, Kenshi; Hirawake, Toru; Yamashita, Youhei

2016-01-01

The spatial distribution of dissolved organic carbon (DOC) concentrations and the optical properties of dissolved organic matter (DOM) determined by ultraviolet-visible absorbance and fluorescence spectroscopy were measured in surface waters of the southern Chukchi Sea, western Arctic Ocean, during the early summer of 2013. Neither the DOC concentration nor the optical parameters of the DOM correlated with salinity. Principal component analysis using the DOM optical parameters clearly separated the DOM sources. A significant linear relationship was evident between the DOC and the principal component score for specific water masses, indicating that a high DOC level was related to a terrigenous source, whereas a low DOC level was related to a marine source. Relationships between the DOC and the principal component scores of the surface waters of the southern Chukchi Sea implied that the major factor controlling the distribution of DOC concentrations was the mixing of plural water masses rather than local production and degradation. PMID:27658444

Spatial and seasonal variability of dissolved organic matter in the Cariaco Basin

NASA Astrophysics Data System (ADS)

Lorenzoni, Laura; Taylor, Gordon T.; Benitez-Nelson, Claudia; Hansell, Dennis A.; Montes, Enrique; Masserini, Robert; Fanning, Kent; Varela, Ramón; Astor, Yrene; GuzmáN, Laurencia; Muller-Karger, Frank E.

2013-06-01

organic carbon (DOC), nitrogen (DON), and phosphorus (DOP) were measured monthly at the CARIACO Time Series station (10°30'N, 64°40'W) in the southeastern Caribbean Sea between 2005 and 2012. Marked seasonal variability in DOC concentrations was observed, with lower values (~66 µM) in the upper water column (<75 m) during the upwelling season (December-April) due to the injection of cool, DOC-impoverished Subtropical Underwater from the Caribbean Sea. During the rainy season (May-November) waters were stratified and upper layer DOC concentrations increased to ~71 µM. Interannual variability in surface (1 m) concentrations of DOC was also observed in response to the variable strength in upwelling and stratification that the Cariaco Basin experienced. DON and DOP showed no such seasonality. At depths >350 m, DOC concentrations were 56 ± 4.7 µM, roughly 10 µM higher than those in the Caribbean Sea over the same depth range. DON and DOP showed similar vertical profiles to that of DOC, with higher concentrations (6.8 ± 1.2 µM N and 0.15 ±0.09 µM P) in the upper water column and invariant, lower concentrations at depth (4.8 ± 1.6 µM N and 0.10 ± 0.08 µM P). Wind-driven advection of surface DOC out of the Cariaco Basin was estimated to support a net export ~15 Gmol C yr-1 into the Caribbean Sea; this rate is comparable to the flux of settling particulate organic carbon to depths >275 m within the basin.

Relationship between the colored dissolved organic matter and dissolved organic carbon and the application on remote sensing in East China Sea

NASA Astrophysics Data System (ADS)

Qiong, Liu; Pan, Delu; Huang, Haiqing; Lu, Jianxin; Zhu, Qiankun

2011-11-01

A cruise was conducted in the East China Sea (ECS) in autumn 2010 to collect Dissolved Organic Carbon (DOC) and Colored Dissolved Organic Matter (CDOM) samples. The distribution of DOC mainly controlled by the hydrography since the relationship between DOC and salinity was significant in both East China Sea. The biological activity had a significant influence on the concentration of DOC with a close correlation between DOC and Chl a. The absorption coefficient of CDOM (a355) decreased with the salinity increasing in the shelf of East China Sea (R2=0.9045). CDOM and DOC were significantly correlated in ECS where DOC distribution was dominated largely by the Changjiang diluted water. Based on the relationship of CDOM and DOC, we estimated the DOC concentration of the surface in ECS from satellite-derived CDOM images. Some deviations induced by the biological effect and related marine DOC accumulations were discussed.

Aeshnid dragonfly larvae as bioindicators of methylmercury contamination in aquatic systems impacted by elevated sulfate loading

USGS Publications Warehouse

Jeremiason, Jeffrey D.; Reiser, T. K.; Weitz, R. A.; Berndt, M.E.; Aiken, George R.

2016-01-01

Methylmercury (MeHg) levels in dragonfly larvae and water were measured over two years in aquatic systems impacted to varying degrees by sulfate releases related to iron mining activity. This study examined the impact of elevated sulfate loads on MeHg concentrations and tested the use of MeHg in dragonfly larvae as an indicator of MeHg levels in a range of aquatic systems including 16 river/stream sites and two lakes. MeHg concentrations in aeshnid dragonfly larvae were positively correlated (R2 = 0.46, p < 0.01) to peak MeHg concentrations in the dissolved phase for the combined years of 2012 and 2013. This relation was strong in 2012 (R2 = 0.85, p < 0.01), but showed no correlation in 2013 (R2 = 0.02, p > 0.05). MeHg in dragonfly larvae were not elevated at the highest sulfate sites, but rather the reverse was generally observed. Record rainfall events in 2012 and above average rainfall in 2013 likely delivered the majority of Hg and MeHg to these systems via interflow and activated groundwater flow through reduced sediments. As a result, the impacts of elevated sulfate releases due to mining activities were not apparent in these systems where little of the sulfate is reduced. Lower bioaccumulation factors for MeHg in aeshnid dragonfly larvae were observed with increasing dissolved organic carbon (DOC) concentrations. This finding is consistent with previous studies showing that MeHg in high DOC systems is less bioavailable; an equilibrium model shows that more MeHg being associated with DOC rather than algae at the base of the food chain readily explains the lower bioaccumulation factors.

The role of DOM in nitrogen processing in streams across arctic regions affected by fire

NASA Astrophysics Data System (ADS)

Rodriguez-Cardona, B.; Schade, J. D.; Holmes, R. M.; Natali, S.; Mann, P. J.; Wymore, A.; Coble, A. A.; Prokishkin, A. S.; Zito, P.; Podgorski, D. C.; Spencer, R. G.; McDowell, W. H.

2017-12-01

In stream ecosystems, inputs of dissolved organic carbon (DOC) have a strong influence on nitrogen (N) processing. Previous studies have demonstrated that increases in DOC concentrations can promote greater N removal in many stream ecosystems. Most of what we know about C and N coupling comes from studies of temperate streams; less is known about this relationship in the Arctic. Streams in Arctic ecosystems are facing rapid changes in climate and disturbance regimes, in particular increasing fire frequencies that are likely to alter biogeochemical cycles. Although fires can lead to increases in NO3 concentrations in streams, the effects of fire on DOC (concentration and composition) have been difficult to generalize. We studied the relationships between DOC and N in two locations; the Central Siberian Plateau, Russia and the Yukon-Kuskokwim (YK) River Delta, Alaska. Streams in both regions show increases in NO3 concentrations after fire, while DOC concentrations decrease in Siberia but increase in streams within the YK-Delta. These patterns in DOC and NO3 create a gradient in DOC and nutrient concentrations, allowing us to study this coupling in a wider Pan-Arctic scope. In order to assess the role of DOC in Arctic N processing, we conducted NO3 and NH4 additions to stream microcosms at the Alaskan site as well as whole-stream additions in Siberia. We hypothesized that nutrient uptake would be high in older burn sites of Siberia and recently burned sites in the YK-Delta, due to greater DOC concentrations and availability. Our results suggest that nitrogen dynamics in the Alaskan sites is strongly responsive to C availability, but is less so in Siberian sites. The potential impacts of permafrost thawing and fires on DOM and nutrient dynamics thus appear to not be consistent across the Arctic suggesting that different regions of the Arctic have unique biogeochemical controls.

Characteristics of wet dissolved carbon deposition in a semi-arid catchment at the Loess Plateau, China

NASA Astrophysics Data System (ADS)

Wang, Linhua; Yen, Haw; Chen, Liding; E, Xinhui; Wang, Yafeng

2018-06-01

Wet dissolved carbon deposition is a critical node of the global carbon cycle, but little is known about dissolved organic and inorganic carbon (DOC and DIC) concentrations and fluxes in the semi-arid areas of the Loess Plateau Region (LPR). In this study, we measured variations in DOC and DIC concentrations in rainfalls at Yangjuangou Ecological Restoration and Soil and Water Observatory. Rainwater samples were collected in 16 rainfall events from July to September and the event-based, monthly concentrations and fluxes of DOC and DIC were quantified. The results showed that the event-based concentrations and fluxes of DOC and DIC were highly variable, ranging from 0.56 to 28.71 mg C L-1 and from 3.47 to 17.49 mg C L-1, respectively. The corresponding event-based fluxes ranged from 0.21-258.36 mg C m-2 and from 4.12 to 42.32 mg C m-2. The monthly concentrations of DOC and DIC were 24.62 and 4.30 (July), 3.58 and 10.52 (August), and 1.01 and 5.89 (September) mg C L-1, respectively. Thus, the monthly deposition fluxes of DOC and DIC were 541.64/94.60, 131.03/385.03, and 44.44/259.16 mg C m-2 for July, August, and September, respectively. In addition, the concentrations of DOC and DIC for the concentrated rainfall season (July-September) in the studied catchment were 7.06 and 7.00 mg C L-1, respectively. The estimated annual wet dissolved carbon depositions were 1.91 and 1.89 g C m-2 yr-1 for DOC and DIC, respectively. The results of this study suggest the variation in concentrations and fluxes of DOC and DIC and explore that these variation may be related to the dissolved carbon source and the rainfall characteristics during the concentrated rainfall season in the semi-arid catchment of the LPR. Furthermore, these results also suggest that dissolved carbon may be an important external input of carbon into terrestrial ecosystems.

Identification and analysis of low molecular weight dissolved organic carbon in subglacial basal ice ecosystems by ion chromatography

NASA Astrophysics Data System (ADS)

Lawson, E. C.; Wadham, J. L.; Lis, G. P.; Tranter, M.; Pickard, A. E.; Stibal, M.; Dewsbury, P.; Fitzsimons, S.

2015-08-01

Glacial runoff is an important source of dissolved organic carbon (DOC) for downstream heterotrophic activity, despite the low overall DOC concentrations. This is because of the abundance of bioavailable, low molecular weight (LMW) DOC species. However, the provenance and character of LMW-DOC is not fully understood. We investigated the abundance and composition of DOC in subglacial environments via a molecular level DOC analysis of basal ice, which forms by water/sediment freeze-on to the glacier sole. Spectrofluorometry and a novel ion chromatographic method, which has been little utilised in glacial science for LMW-DOC determinations, were employed to identify and quantify the major LMW fractions (free amino acids, carbohydrates and carboxylic acids) in basal ice from four glaciers, each with a different basal debris type. Basal ice from Joyce Glacier (Antarctica) was unique in that 98 % of the LMW-DOC was derived from the extremely diverse FAA pool, comprising 14 FAAs. LMW-DOC concentrations in basal ice were dependent on the bioavailability of the overridden organic carbon (OC), which in turn, was influenced by the type of overridden material. Mean LMW-DOC concentrations in basal ice from Russell Glacier (Greenland), Finsterwalderbreen (Svalbard) and Engabreen (Norway) were low (0-417 nM C), attributed to the relatively refractory nature of the OC in the overridden paleosols and bedrock. In contrast, mean LMW-DOC concentrations were an order of magnitude higher (4430 nM C) in basal ice from Joyce Glacier, a reflection of the high bioavailability of the overridden lacustrine material (>17 % of the sediment OC comprised extractable carbohydrates, a proxy for bioavailable OC). We find that the overridden material may act as a direct (via abiotic leaching) and indirect (via microbial cycling) source of DOC to the subglacial environment and provides a range of LMW-DOC compounds that may stimulate microbial activity in wet sediments in current subglacial environments.

Partial coupling and differential regulation of biologically and photo-chemically labile dissolved organic carbon across boreal aquatic networks

NASA Astrophysics Data System (ADS)

Lapierre, J.-F.; del Giorgio, P. A.

2014-05-01

Despite the rapidly increasing volume of research on the biological and photochemical degradation of DOC in aquatic environments, little is known on the large-scale patterns in biologically and photo-chemically degradable DOC (Bd-DOC and Pd-DOC, respectively) in continental watersheds, and on the links that exist between these two key properties that greatly influence the flow of carbon from continents to oceans. Here we explore the patterns of Bd- and Pd-DOC across hundreds of boreal lakes, rivers and wetlands spanning a large range of system trophy and terrestrial influence, and compared the drivers of these two reactive pools of DOC at the landscape level. Using standardized incubations of natural waters, we found that the concentrations of Bd- and Pd-DOC co-varied across all systems studied but were nevertheless related to different pools of dissolved organic matter (DOM, identified by fluorescence analyses) in ambient waters. A combination of nutrients and protein-like DOM explained nearly half of the variation in Bd-DOC, whereas Pd-DOC was exclusively predicted by DOM optical properties, consistent with the photochemical degradability of specific fluorescent DOM (FDOM) pools that we experimentally determined. The concentrations of colored DOM (CDOM), a proxy of terrestrial influence, almost entirely accounted for the observed relationship between FDOM and the concentrations of both Bd- and Pd-DOC. The concentrations of CDOM and of the putative bio-labile fluorescence component shifted from complete decoupling in clear-water environments to strong coupling in browner streams and wetlands. This suggests a baseline autochthonous Bd-DOC pool fuelled by internal production that is gradually overwhelmed by land-derived Bd-DOC as terrestrial influence increases across landscape gradients. The importance of land as a major source of both biologically and photo-chemically degradable DOC for continental watersheds resulted in a partial coupling of those carbon pools in natural freshwaters, despite fundamental contrasts in terms of their composition and regulation.

[Characteristics of dissolved organic carbon release under inundation from typical grass plants in the water-level fluctuation zone of the Three Gorges Reservoir area].

PubMed

Tan, Qiu-Xia; Zhu, Boi; Hua, Ke-Ke

2013-08-01

The water-level fluctuation zone of the Three Gorges Reservoir (TGR) exposes in spring and summer, then, green plants especially herbaceous plants grow vigorously. In the late of September, water-level fluctuation zone of TGR goes to inundation. Meanwhile, annually accumulated biomass of plant will be submerged for decaying, resulting in organism decomposition and release a large amount of dissolved organic carbon (DOC). This may lead to negative impacts on water environment of TGR. The typical herbaceous plants from water-level fluctuation zone were collected and inundated in the laboratory for dynamic measurements of DOC concentration of overlying water. According to the determination, the DOC release rates and fluxes have been calculated. Results showed that the release process of DOC variation fitted in a parabolic curve. The peak DOC concentrations emerge averagely in the 15th day of inundation, indicating that DOC released quickly with organism decay of herbaceous plant. The release process of DOC could be described by the logarithm equation. There are significant differences between the concentration of DOC (the maximum DOC concentration is 486.88 mg x L(-1) +/- 35.97 mg x L(-1) for Centaurea picris, the minimum is 4.18 mg x L(-1) +/- 1.07 mg x L(-1) for Echinochloacrus galli) and the release amount of DOC (the maximum is 50.54 mg x g(-1) for Centaurea picris, the minimum is 6.51 mg x g(-1) for Polygonum hydropiper) due to different characteristics of plants, especially, the values of C/N of herbaceous plants. The cumulative DOC release quantities during the whole inundation period were significantly correlated with plants' C/N values in linear equations.

Broad-scale predictability of carbohydrates and exopolymers in Antarctic and Arctic sea ice

PubMed Central

Underwood, Graham J. C.; Aslam, Shazia N.; Michel, Christine; Niemi, Andrea; Norman, Louiza; Meiners, Klaus M.; Laybourn-Parry, Johanna; Paterson, Harriet; Thomas, David N.

2013-01-01

Sea ice can contain high concentrations of dissolved organic carbon (DOC), much of which is carbohydrate-rich extracellular polymeric substances (EPS) produced by microalgae and bacteria inhabiting the ice. Here we report the concentrations of dissolved carbohydrates (dCHO) and dissolved EPS (dEPS) in relation to algal standing stock [estimated by chlorophyll (Chl) a concentrations] in sea ice from six locations in the Southern and Arctic Oceans. Concentrations varied substantially within and between sampling sites, reflecting local ice conditions and biological content. However, combining all data revealed robust statistical relationships between dCHO concentrations and the concentrations of different dEPS fractions, Chl a, and DOC. These relationships were true for whole ice cores, bottom ice (biomass rich) sections, and colder surface ice. The distribution of dEPS was strongly correlated to algal biomass, with the highest concentrations of both dEPS and non-EPS carbohydrates in the bottom horizons of the ice. Complex EPS was more prevalent in colder surface sea ice horizons. Predictive models (validated against independent data) were derived to enable the estimation of dCHO concentrations from data on ice thickness, salinity, and vertical position in core. When Chl a data were included a higher level of prediction was obtained. The consistent patterns reflected in these relationships provide a strong basis for including estimates of regional and seasonal carbohydrate and dEPS carbon budgets in coupled physical-biogeochemical models, across different types of sea ice from both polar regions. PMID:24019487

Broad-scale predictability of carbohydrates and exopolymers in Antarctic and Arctic sea ice.

PubMed

Underwood, Graham J C; Aslam, Shazia N; Michel, Christine; Niemi, Andrea; Norman, Louiza; Meiners, Klaus M; Laybourn-Parry, Johanna; Paterson, Harriet; Thomas, David N

2013-09-24

Sea ice can contain high concentrations of dissolved organic carbon (DOC), much of which is carbohydrate-rich extracellular polymeric substances (EPS) produced by microalgae and bacteria inhabiting the ice. Here we report the concentrations of dissolved carbohydrates (dCHO) and dissolved EPS (dEPS) in relation to algal standing stock [estimated by chlorophyll (Chl) a concentrations] in sea ice from six locations in the Southern and Arctic Oceans. Concentrations varied substantially within and between sampling sites, reflecting local ice conditions and biological content. However, combining all data revealed robust statistical relationships between dCHO concentrations and the concentrations of different dEPS fractions, Chl a, and DOC. These relationships were true for whole ice cores, bottom ice (biomass rich) sections, and colder surface ice. The distribution of dEPS was strongly correlated to algal biomass, with the highest concentrations of both dEPS and non-EPS carbohydrates in the bottom horizons of the ice. Complex EPS was more prevalent in colder surface sea ice horizons. Predictive models (validated against independent data) were derived to enable the estimation of dCHO concentrations from data on ice thickness, salinity, and vertical position in core. When Chl a data were included a higher level of prediction was obtained. The consistent patterns reflected in these relationships provide a strong basis for including estimates of regional and seasonal carbohydrate and dEPS carbon budgets in coupled physical-biogeochemical models, across different types of sea ice from both polar regions.

Dissolved Organic Carbon in Headwater Streams and Riparian Soil Organic Carbon along an Altitudinal Gradient in the Wuyi Mountains, China

PubMed Central

Huang, Wei; McDowell, William H.; Zou, Xiaoming; Ruan, Honghua; Wang, Jiashe; Li, Liguang

2013-01-01

Stream water dissolved organic carbon (DOC) correlates positively with soil organic carbon (SOC) in many biomes. Does this relationship hold in a small geographic region when variations of temperature, precipitation and vegetation are driven by a significant altitudinal gradient? We examined the spatial connectivity between concentrations of DOC in headwater stream and contents of riparian SOC and water-soluble soil organic carbon (WSOC), riparian soil C:N ratio, and temperature in four vegetation types along an altitudinal gradient in the Wuyi Mountains, China. Our analyses showed that annual mean concentrations of headwater stream DOC were lower in alpine meadow (AM) than in subtropical evergreen broadleaf forest (EBF), coniferous forest (CF), and subalpine dwarf forest (SDF). Headwater stream DOC concentrations were negatively correlated with riparian SOC as well as WSOC contents, and were unrelated to riparian soil C:N ratio. Our findings suggest that DOC concentrations in headwater streams are affected by different factors at regional and local scales. The dilution effect of higher precipitation and adsorption of soil DOC to higher soil clay plus silt content at higher elevation may play an important role in causing lower DOC concentrations in AM stream of the Wuyi Mountains. Our results suggest that upscaling and downscaling of the drivers of DOC export from forested watersheds when exploring the response of carbon flux to climatic change or other drivers must done with caution. PMID:24265737

Controls on dissolved organic carbon quantity and chemical character in temperate rivers of North America

USGS Publications Warehouse

Hanley, Kevin W.; Wollheim, Wilfred M.; Salisbury, Joseph; Huntington, Thomas G.; Aiken, George R.

2013-01-01

Understanding the processes controlling the transfer and chemical composition of dissolved organic carbon (DOC) in freshwater systems is crucial to understanding the carbon cycle and the effects of DOC on water quality. Previous studies have identified watershed-scale controls on bulk DOC flux and concentration among small basins but fewer studies have explored controls among large basins or simultaneously considered the chemical composition of DOC. Because the chemical character of DOC drives riverine biogeochemical processes such as metabolism and photodegradation, accounting for chemical character in watershed-scale studies will improve the way bulk DOC variability in rivers is interpreted. We analyzed DOC quantity and chemical character near the mouths of 17 large North American rivers, primarily between 2008 and 2010, and identified watershed characteristics that controlled variability. We quantified DOC chemical character using both specific ultraviolet absorbance at 254 nm (SUVA254) and XAD-resin fractionation. Mean DOC concentration ranged from 2.1 to 47 mg C L−1 and mean SUVA254 ranged from 1.3 to 4.7 L mg C−1 m−1. We found a significant positive correlation between basin wetland cover and both bulk DOC concentration (R2 = 0.78; p < 0.0001) and SUVA254 (R2 = 0.91; p < 0.0001), while other land use characteristics were not correlated. The strong wetland relationship with bulk DOC concentration is similar to that found by others in small headwater catchments. However, two watersheds with extremely long surface water residence times, the Colorado and St. Lawrence, diverged from this wetland relationship. These results suggest that the role of riverine processes in altering the terrestrial DOC signal at the annual scale was minimal except in river systems with long surface water residence times. However, synoptic DOC sampling of both quantity and character throughout river networks will be needed to more rigorously test this finding. The inclusion of DOC chemical character will be vital to achieving a more complete understanding of bulk DOC dynamics in large river systems.

Investigating Forest Harvest Effects on DOC Concentration and Quality: An In Situ, High Resolution Approach to Quantifying DOC Export Dynamics

NASA Astrophysics Data System (ADS)

Jollymore, A. J.; Johnson, M. S.; Hawthorne, I.

2013-12-01

Justification: Forest harvest effects on water quality can signal alterations in hydrologic and ecologic processes incurred as a result of forest harvest activities. Organic matter (OM), specifically dissolved organic carbon (DOC), plays a number of important roles mediating UV-light penetration, redox reactivity and microbial activity within aquatic ecosystems. Quantification of DOC is typically pursued via grab sampling followed by chemical or spectrophotometric analysis, limiting the temporal resolution obtained as well as the accuracy of export calculations. The advent of field-deployable sensors capable of measuring DOC concentration and certain quality characteristics in situ provides the ability to observe dynamics at temporal scales necessary for accurate calculation of DOC flux, as well as the observation of dynamic changes in DOC quality on timescales impossible to observe through grab sampling. Methods: This study utilizes a field deployable UV-Vis spectrophotometer (spectro::lyzer, s::can, Austria) to investigate how forest harvest affects DOC export. The sensor was installed at an existing hydrologic monitoring site at the outlet of a headwater stream draining a small (91 hectare) second growth Douglasfir-dominated catchment near Campbell River on Vancouver Island, British Columbia. Measurement began late in 2009, prior to forest harvest and associated activities such as road building (which commenced in October 2010 and ended in early 2011), and continues to present. During this time - encompassing the pre, during and post-harvest conditions - the absorbance spectrum of stream water from 200 to 750 nm was measured. DOC concentration and spectroscopic indices related to DOC quality (including SUVA, which relates to the concentration of aromatic carbon, and spectral slope) were subsequently calculated for each spectra obtained at 30-minute intervals. Results and conclusions: High frequency measurements of DOC show that overall export of OM increased in the months following harvest. A major advantage of this study is the use of in situ measurements, allowing for high temporal resolution of DOC dynamics occurring within specific hydrologic events. For example, concentration-discharge relationships for both the pre- and post-logging periods demonstrate similar clockwise hysteresis during individual storm events, while the magnitude of change dramatically increased during the post-logging period. However, in situ measurements of SUVA over this period suggest that DOC quality may be less affected by forest harvest than overall DOC concentration, where high frequency data also allows for the observation of SUVA and spectral slope responses to specific hydrologic events during the pre- and post- harvest period.

Drivers of inverse DOC-nitrate loss patterns in forest soils and streams

NASA Astrophysics Data System (ADS)

Goodale, C. L.

2013-12-01

Nitrate loss from forested catchments varies greatly across sites and over time, with few reliable correlates. One of the few recurring patterns, however, is the negative nonlinear relationship that occurs regularly between surface water nitrate and dissolved organic carbon (DOC) concentrations: that is, nitrate declines sharply as DOC concentrations increase, and high nitrate levels occur only at low DOC concentrations. Several hypotheses have been proposed to explain this pattern, but its cause has remained speculative. It is likely to be driven by C- or N-limitation of biological processes such as assimilation or denitrification, but the identity of which biological process or the main landscape position of their activity are not known. We examined whether DOC and nitrate are both driven by soil C content, at scales of both soil blocks and across catchments, by measuring soil, soil extract, and surface water chemistry across nine catchments selected from long-term monitoring networks in the Catskill and Adirondack Mountains. We measured soil C and N status and solution nitrate, DOC, bioavailable DOC (bDOC), and isotopic composition (13C-DOC, 15N- and 18O-NO3) to examine whether variation in stocks of soil C partly controls DOC and nitrate loss from forested catchments in New York State. These measurements showed that surface soil C and C:N ratio together determine soil production of DOC and nitrate, reflecting assimilative demand for N by heterotrophic microbes. Yet, they also show that these processes do not produce the inverse DOC-NO3 curve observed at the catchment scale. Rather, catchment-scale DOC-nitrate patterns are more likely to be governed by the balance between excess nitrate production and its bDOC-mediated loss to denitrification.

Regional variation in the biogeochemical and physical characteristics of natural peatland pools.

PubMed

Turner, T Edward; Billett, Michael F; Baird, Andy J; Chapman, Pippa J; Dinsmore, Kerry J; Holden, Joseph

2016-03-01

Natural open-water pools are a common feature of northern peatlands and are known to be an important source of atmospheric methane (CH4). Pool environmental variables, particularly water chemistry, vegetation community and physical characteristics, have the potential to exert strong controls on carbon cycling in pools. A total of 66 peatland pools were studied across three regions of the UK (northern Scotland, south-west Scotland, and Northern Ireland). We found that within-region variability of pool water chemistry was low; however, for many pool variables measured there were significant differences between regions. PCA analysis showed that pools in SW Scotland were strongly associated with greater vegetative cover and shallower water depth which is likely to increase dissolved organic carbon (DOC) mineralisation rates, whereas pools in N Scotland were more open and deeper. Pool water DOC, particulate organic carbon and dissolved CH4 concentrations were significantly different between regions. Pools in Northern Ireland had the highest concentrations of DOC (mean=14.5 mg L(-1)) and CH4 (mean=20.6 μg C L(-1)). Chloride and sulphate concentrations were significantly higher in the pools in N Scotland (mean values 26.3 and 2.40 mg L(-1), respectively) than elsewhere, due to a stronger marine influence. The ratio of UV absorbance at 465 nm to absorbance at 665 nm for pools in Northern Ireland indicated that DOC was sourced from poorly humified peat, potentially increasing the bioavailability and mineralisation of organic carbon in pools compared to the pools elsewhere. This study, which specifically aims to address a lack of basic biogeochemical knowledge about pool water chemistry, clearly shows that peatland pools are highly regionally variable. This is likely to be a reflection of significant regional-scale differences in peatland C cycling. Copyright © 2015 Elsevier B.V. All rights reserved.

Effect of Photochemical Transformation on Dissolved Organic Carbon Concentration and Bioavailability from Watersheds with Varying Landcover

NASA Astrophysics Data System (ADS)

Vermilyea, A.; Sanders, A.; Vazquez, E.

2017-12-01

The transformation of freshwater dissolved organic carbon (DOC) can have important implications for water quality, aquatic ecosystem health, and our climate. DOC is an important nutrient for heterotrophic microorganisms near the base of the aquatic food chain and the extent of conversion of DOC to CO2 is a critical piece of the global carbon cycle. Photochemical pathways have the potential to transform recalcitrant DOC into more labile forms that can then be converted to smaller DOC molecules and eventually be completely mineralized to CO2. This may lead to a DOC pool with different bioavailability depending on the structural composition of the original DOC pool and the mechanistic pathways undergone during transformation. This study aimed to measure the changes in DOC concentration and bioavailability due solely to photochemical processes in three watersheds of northern Vermont, USA that have varied land cover, land use (LCLU) attributes. Our hypothesis was that photochemical transformations will lead to (1) an overall loss of DOC due to mineralization to CO2 and (2) a relative increase in the bioavailable fraction of DOC. Additionally, the influence of LCLU and base flow versus storm flow on both mineralization rates and changes in DOC bioavailability was investigated. Irradiation of filtered samples in quartz vessels under sunlight led to small changes in DOC concentration over time, but significant changes in DOC bioavailability. In general, fluorescence excitation-emission matrices (EEMs) showed a shift from an initially more humic-like DOC pool, to a more protein-like (bioavailable) DOC pool. Specific UV index (SUVA) along with bioavailable DOC (BDOC) incubations were also used to characterize DOC and its bioavailability. There were only small differences in the DOC transformation that took place among sites, possibly due to only small differences in the initial bioavailability and fluorescent properties between water samples. Photochemical transformation appears to play an important role in the transformation of a more recalcitrant (humic) pool of DOC into a more bioavailable DOC pool that can then be utilized by aquatic heterotrophs and ultimately be converted to CO2.

Wetlands receiving water treated with coagulants improve water quality by removing dissolved organic carbon and disinfection byproduct precursors.

PubMed

Hansen, Angela M; Kraus, Tamara E C; Bachand, Sandra M; Horwath, William R; Bachand, Philip A M

2018-05-01

Constructed wetlands are used worldwide to improve water quality while also providing critical wetland habitat. However, wetlands have the potential to negatively impact drinking water quality by exporting dissolved organic carbon (DOC) that upon disinfection can form disinfection byproducts (DBPs) like trihalomethanes (THMs) and haloacetic acids (HAAs). We used a replicated field-scale study located on organic rich soils in California's Sacramento-San Joaquin Delta to test whether constructed flow-through wetlands which receive water high in DOC that is treated with either iron- or aluminum-based coagulants can improve water quality with respect to DBP formation. Coagulation alone removed DOC (66-77%) and THM (67-70%) precursors, and was even more effective at removing HAA precursors (77-90%). Passage of water through the wetlands increased DOC concentrations (1.5-7.5mgL -1 ), particularly during the warmer summer months, thereby reversing some of the benefits from coagulant addition. Despite this addition, water exiting the wetlands treated with coagulants had lower DOC and DBP precursor concentrations relative to untreated source water. Benefits of the coagulation-wetland systems were greatest during the winter months (approx. 50-70% reduction in DOC and DBP precursor concentrations) when inflow water DOC concentrations were higher and wetland DOC production was lower. Optical properties suggest DOC in this system is predominantly comprised of high molecular weight, aromatic compounds, likely derived from degraded peat soils. Published by Elsevier B.V.

Export and losses of blue carbon-derived particulate and dissolved organic carbon (POC and DOC) in blackwater river-dominated and particle-dominated estuaries

NASA Astrophysics Data System (ADS)

Arellano, A. R.; Bianchi, T. S.; Osburn, C. L.; D'Sa, E. J.; Oviedo Vargas, D.; Ward, N. D.; Joshi, I.; Ko, D. S.

2016-12-01

Globally, coastal blue carbon environments (wetlands, seagrass beds and mangroves) sequester an estimated 67-215 Tg C yr-1. While most blue carbon research has focused on carbon burial/stocks and habitat fragmentation of these communities, few studies have examined the export and loss of blue carbon sources of particulate organic matter (POM) and dissolved organic matter (DOM) to adjacent coastal waters. These shifts in losses of DOM and POM are also partly due to large-scale changes in land-use and climate change. Due to the complexity of vascular plant inputs to estuarine systems (e.g. terrestrial vs. blue carbon), being able to separate blue carbon sources of POM and DOM are critical. Here, we investigate the temporal variability of the abundance, sources and breakdown of particulate and dissolved organic carbon (POC and DOC) in particle-dominated (Barataria Bay) and blackwater river-dominated (Apalachicola Bay) estuaries in the northern Gulf of Mexico, using bulk carbon, dissolved lignin phenols, δ13C and dissolved CO2. The range of DOC:POC ratios for Barataria and Apalachicola bays were 0.5-3.1 and 2.3-57.0, respectively. δ13C-POC values were more depleted in Apalachicola (x̅=-27.3‰) compared to those in Barataria (x̅=-24.8‰), and C:N ratios were higher in Apalachicola (x̅=10.8) than in Barataria (x̅=9.3). Although there was no significant temporal variability with δ13C-POC in both systems, Barataria Bay had the highest POC (0.08-0.23 mM) and C:N (7.0-13.4) values during spring, when enhanced southerly winds likely resulted in higher resuspension and marsh erosion rates. Additionally, in Apalachicola, the lowest C:N values (6.2-16.1) were observed during the dry season when fluvial DOM inputs were minimal. The highest dissolved lignin phenol and DOC (0.10-2.98 mM) concentrations in Apalachicola occurred during the wet season, reflecting the importance of riverine inputs to this system. In particular, the Carabelle River plume region had C:V and S:V values that indicated woody inputs (long-leaf pine communities), while the bay proper/East Bay were more indicative of blue carbon sources. Spatial and temporal variability of dissolved CO2 concentrations will be discussed as it relates to possible linkages with the export and losses of blue carbon-derived DOC and POC.

Organic and inorganic carbon dynamics in a karst aquifer: Santa Fe River Sink-Rise system, north Florida, USA

NASA Astrophysics Data System (ADS)

Jin, Jin; Zimmerman, Andrew R.; Moore, Paul J.; Martin, Jonathan B.

2014-03-01

Spatiotemporal variations in dissolved organic carbon (DOC), dissolved inorganic carbon (DIC), major ions concentrations and other geochemical parameters including stable carbon isotopes of DIC (δ13CDIC), were measured in surface water and deep and shallow well water samples of the Santa Fe River Sink-Rise eogenetic karst system, north Florida, USA. Three end-member water sources were identified: one DOC-rich/DIC-poor/δ13CDIC-depleted, one DOC-poor/DIC-rich/δ13CDIC-enriched, and one enriched in major ions. Given their spatiotemporal distributions, they were presumed to represent soil water, upper aquifer groundwater, and deep aquifer water sources, respectively. Using assumed ratios of Na+, Cl, and SO42- for each end-member, a mixing model calculated the contribution of each water source to each sample. Then, chemical effects of biogeochemical reactions were calculated as the difference between those predicted by the mixing model and measured species concentrations. In general, carbonate mineral dissolution occurred throughout the Sink-Rise system, surface waters were net autotrophic and the subsurface was in metabolic balance, i.e., no net DOC or DIC production or consumption. However, there was evidence for chemolithoautotrophy, perhaps by hydrogen oxidizing microbes, at some deep aquifer sites. Mineralization of this autochthonous natural dissolved organic matter (NDOM) led to localized carbonate dissolution as did surface water-derived NDOM supplied to shallow well sites during the highest flow periods. This study demonstrates linkages between hydrology, abiotic and microbial processes and carbon dynamics and has important implications for groundwater quality, karst morphologic evolution, and hydrogeologic projects such as aquifer storage and recovery in karst systems.

The soil organic carbon content of anthropogenically altered organic soils effects the dissolved organic matter quality, but not the dissolved organic carbon concentrations

NASA Astrophysics Data System (ADS)

Frank, Stefan; Tiemeyer, Bärbel; Bechtold, Michel; Lücke, Andreas; Bol, Roland

2016-04-01

Dissolved organic carbon (DOC) is an important link between terrestrial and aquatic ecosystems. This is especially true for peatlands which usually show high concentrations of DOC due to the high stocks of soil organic carbon (SOC). Most previous studies found that DOC concentrations in the soil solution depend on the SOC content. Thus, one would expect low DOC concentrations in peatlands which have anthropogenically been altered by mixing with sand. Here, we want to show the effect of SOC and groundwater level on the quantity and quality of the dissolved organic matter (DOM). Three sampling sites were installed in a strongly disturbed bog. Two sites differ in SOC (Site A: 48%, Site B: 9%) but show the same mean annual groundwater level of 15 and 18 cm below ground, respectively. The SOC content of site C (11%) is similar to Site B, but the groundwater level is much lower (-31 cm) than at the other two sites. All sites have a similar depth of the organic horizon (30 cm) and the same land-use (low-intensity sheep grazing). Over two years, the soil solution was sampled bi-weekly in three depths (15, 30 and 60 cm) and three replicates. All samples were analyzed for DOC and selected samples for dissolved organic nitrogen (DON) and delta-13C and delta-15N. Despite differences in SOC and groundwater level, DOC concentrations did not differ significantly (A: 192 ± 62 mg/L, B: 163 ± 55 mg/L and C: 191 ± 97 mg/L). At all sites, DOC concentrations exceed typical values for peatlands by far and emphasize the relevance even of strongly disturbed organic soils for DOC losses. Individual DOC concentrations were controlled by the temperature and the groundwater level over the preceding weeks. Differences in DOM quality were clearer. At site B with a low SOC content, the DOC:DON ratio of the soil solution equals the soil's C:N ratio, but the DOC:DON ratio is much higher than the C:N ratio at site A. In all cases, the DOC:DON ratio strongly correlates with delta-13C. There is no isotope data for site C. Delta-15N is more enriched at site B than at site A, indicating differences in C and N cycling and potential influence of the dominant vegetation (grasses vs. Sphagnum mosses).

Landscape control on the hydrogeochemistry of As, Co and Pb in a boreal stream network

NASA Astrophysics Data System (ADS)

Wällstedt, Teresia; Björkvald, Louise; Laudon, Hjalmar; Borg, Hans; Mörth, Carl-Magnus

2017-08-01

In a boreal stream network, stream water concentrations of As, Co and Pb (filtered, <0.4 μm) of 10 nested streams were studied during two consecutive years in order to evaluate the influence of land cover on the temporal and spatial variability of metal concentrations and speciation. Mean concentrations of Co and Pb showed significant but contrasting relationship to landscape type, while As concentrations were not related to landscape type. Highest concentrations of Pb were found in the wetland dominated streams (>30% wetland), which was suggested to be controlled by atmospheric deposition in combination with high DOC release from the wetlands. For Co, the highest concentrations were found in the forest dominated sites (>98% forest), which were attributed to the weathering of minerogenic sources. Contrasting response to runoff events could also be related to landscape type; during the spring flood, decreasing concentrations of As, Co and Pb were observed in the wetland dominated catchments due to dilution, while increasing concentrations during spring flood were observed in the mixed catchments (2-30% wetland) and to some degree in the forested catchments, probably due to flushing of the organic-rich riparian sources. Further, metal speciation was calculated using the geochemical equilibrium model Visual MINTEQ. This suggests that dissolved inorganic species of As and Co dominated in headwater streams with low pH while DOC had a major influencing role for Pb. In the larger mixed streams where pH was higher and precipitation of e.g. colloidal Fe and Mn (hydr)oxides was favoured, the major influencing factor was instead adsorption to colloidal Fe for As and Pb, while association to organic matter and colloids of e.g. Mn influenced the concentrations of Co. We thus conclude that landscape type and the magnitude of the runoff events are of great importance for the spatial and temporal variations of As, Co and Pb in this boreal stream network. Projected climate change, with increasing runoff, may therefore influence riverine concentrations and fluxes differently, depending on the prevailing landscape type.

ORCHIDEE-SOM: modeling soil organic carbon (SOC) and dissolved organic carbon (DOC) dynamics along vertical soil profiles in Europe

NASA Astrophysics Data System (ADS)

Camino-Serrano, Marta; Guenet, Bertrand; Luyssaert, Sebastiaan; Ciais, Philippe; Bastrikov, Vladislav; De Vos, Bruno; Gielen, Bert; Gleixner, Gerd; Jornet-Puig, Albert; Kaiser, Klaus; Kothawala, Dolly; Lauerwald, Ronny; Peñuelas, Josep; Schrumpf, Marion; Vicca, Sara; Vuichard, Nicolas; Walmsley, David; Janssens, Ivan A.

2018-03-01

Current land surface models (LSMs) typically represent soils in a very simplistic way, assuming soil organic carbon (SOC) as a bulk, and thus impeding a correct representation of deep soil carbon dynamics. Moreover, LSMs generally neglect the production and export of dissolved organic carbon (DOC) from soils to rivers, leading to overestimations of the potential carbon sequestration on land. This common oversimplified processing of SOC in LSMs is partly responsible for the large uncertainty in the predictions of the soil carbon response to climate change. In this study, we present a new soil carbon module called ORCHIDEE-SOM, embedded within the land surface model ORCHIDEE, which is able to reproduce the DOC and SOC dynamics in a vertically discretized soil to 2 m. The model includes processes of biological production and consumption of SOC and DOC, DOC adsorption on and desorption from soil minerals, diffusion of SOC and DOC, and DOC transport with water through and out of the soils to rivers. We evaluated ORCHIDEE-SOM against observations of DOC concentrations and SOC stocks from four European sites with different vegetation covers: a coniferous forest, a deciduous forest, a grassland, and a cropland. The model was able to reproduce the SOC stocks along their vertical profiles at the four sites and the DOC concentrations within the range of measurements, with the exception of the DOC concentrations in the upper soil horizon at the coniferous forest. However, the model was not able to fully capture the temporal dynamics of DOC concentrations. Further model improvements should focus on a plant- and depth-dependent parameterization of the new input model parameters, such as the turnover times of DOC and the microbial carbon use efficiency. We suggest that this new soil module, when parameterized for global simulations, will improve the representation of the global carbon cycle in LSMs, thus helping to constrain the predictions of the future SOC response to global warming.

Fingerprinting Dissolved Organic Carbon (DOC) Sources with Specific UV Absorbance (SUVA) and Fluorescence

NASA Astrophysics Data System (ADS)

van Verseveld, W. J.; Lajtha, K.; McDonnell, J. J.

2007-12-01

DOC is an important water quality constituent because it is an important food source for stream biota, it plays a significant role in metal toxicity and transport, and protects aquatic organisms by absorbing visible and UV light. However, sources of stream DOC and changes in DOC quality at storm and seasonal scales remain poorly understood. We characterized DOC concentrations and SUVA (as an indicator of aromaticity) at the plot, hillslope and catchment scale during and between five storm events over the period Fall 2004 until Spring 2005, in WS10, H.J. Andrews, Oregon, USA. This study site has hillslopes that issue directly into the stream. This enabled us to compare a trenched hillslope response to the stream response without the influence of a riparian zone. The main result of this study was that SUVA in addition to DOC was needed to fingerprint sources of DOC. Stream water and lateral subsurface flow showed a clockwise DOC and SUVA hysteresis pattern. Both organic horizon water and transient groundwater were characterized by high DOC concentrations and SUVA values, while DOC concentrations and SUVA values in soil water decreased with depth in the soil profile. This indicates transient groundwater was an important contributor to high DOC concentrations and SUVA values during storm events. During the falling limb of the hydrograph deep soil water and seepage groundwater based on SUVA values contributed significantly to lateral subsurface flow and stream water. Preliminary results showed that fluorescence of stream water and lateral subsurface flow continuously measured with a fluorometer was significantly related to UV-absorbance during a December storm event. Finally, SUVA of lateral subsurface flow was lower than SUVA of stream water at the seasonal scale, indicating a difference in mixing of water sources at the hillslope and catchment scale. Overall, our results show that SUVA and fluorescence are useful tracers for fingerprinting DOC sources.

Dissolved Organic Carbon along the Louisiana coast from MODIS and MERIS satellite data

NASA Astrophysics Data System (ADS)

Chaichi Tehrani, N.; D'Sa, E. J.

2012-12-01

Dissolved organic carbon (DOC) plays a critical role in the coastal and ocean carbon cycle. Hence, it is important to monitor and investigate its the distribution and fate in coastal waters. Since DOC cannot be measured directly through satellite remote sensors, chromophoric dissolved organic matter (CDOM) as an optically active fraction of DOC can be used as an alternative proxy to trace DOC concentrations. Here, satellite ocean color data from MODIS, MERIS, and field measurements of CDOM and DOC were used to develop and assess CDOM and DOC ocean color algorithms for coastal waters. To develop a CDOM retrieval algorithm, empirical relationships between CDOM absorption coefficient at 412 nm (aCDOM(412)) and reflectance ratios Rrs(488)/Rrs(555) for MODIS and Rrs(510)/Rrs(560) for MERIS were established. The performance of two CDOM empirical algorithms were evaluated for retrieval of (aCDOM(412)) from MODIS and MERIS in the northern Gulf of Mexico. Further, empirical algorithms were developed to estimate DOC concentration using the relationship between in situ aCDOM(412) and DOC, as well as using the newly developed CDOM empirical algorithms. Accordingly, our results revealed that DOC concentration was strongly correlated to aCDOM (412) for summer and spring-winter periods (r2 = 0.9 for both periods). Then, using the aCDOM(412)-Rrs and the aCDOM(412)-DOC relationships derived from field measurements, a relationship between DOC-Rrs was established for MODIS and MERIS data. The DOC empirical algorithms performed well as indicated by match-up comparisons between satellite estimates and field data (R2=0.52 and 0.58 for MODIS and MERIS for summer period, respectively). These algorithms were then used to examine DOC distribution along the Louisiana coast.

Concentration and age of DOC transported from thawing permafrost soils into Arctic headwater streams

NASA Astrophysics Data System (ADS)

Romano, E. L.; Wickland, K.; Ebert, C.; Schuur, E.

2017-12-01

As Arctic permafrost stability decreases due to global climate change, hydrologic dynamics in catchments underlain by permafrost are expected to shift. The thickness of seasonally thawed surface soils is an important driver of the extent to which carbon (C) that was previously stored as frozen soil organic carbon (SOC) will be transported laterally as dissolved organic carbon (DOC). The concentration and radiocarbon (14C) age of newly thawed DOC that moves downslope through tundra soils and is delivered to headwater streams is an important indicator of changing C dynamics. Understanding the timing and quantity of C loss in this form is imperative for greenhouse gas emission and soil C stock estimates, as well as predicting the impact of permafrost thaw on aquatic ecosystems. In this study we examined the relationship between DOC concentrations, 14C-DOC, and active layer thickness (ALT) in thawing soils over time. Water samples were collected once in July 2016 and weekly in 2017 from late May to late August from wells within a long-term tundra soil warming experiment (n=36), located in a discontinuous permafrost zone in Interior Alaska. Preliminary data from 2016 shows average maximum ALT at wells within the warming treatment of 68.9 cm, while wells from control averaged 86.6 cm. 2016 water sample data from wells within the warming treatment showed higher mean DOC concentrations (103.1 ± 32.5 mg/L) and older 14C-DOC values (-28.7 ± 21.1 ‰) than samples from the control (44.5 ± 3.0 mg/L and 11.3 ± 8.6 ‰). To assess inter-annual changes in DOC delivery to local headwater streams, DOC concentration and 14C-DOC were also measured on water samples taken in late summer of 2007, 2008, and 2016 from streams within the watershed surrounding the experimental sites. Weekly sampling in 2017 allowed analysis of seasonal patterns of DOC concentration for that year. Values increased slightly over time at some stream sites (ranging from 4-33 mg/L in 2012 to 2-80 mg/L in 2016). Seasonal and inter-annual permafrost thaw appears to drive the release of previously stored old C in the form of DOC, which increases downslope mobility. In-situ terrestrial greenhouse gas emission estimates may therefore underestimate C losses, especially when precipitation is high or early in the season when spring snowmelt and shallow ALT promote lateral transport of DOC.

The Role of Alpine Wetlands as Hot Spots of Dissolved Organic Carbon Fluxes in the East River, Colorado

NASA Astrophysics Data System (ADS)

Winnick, M.; Rainaldi, G. R.; Lawrence, C. R.; McCormick, M. E.; Hsu, H. T.; Druhan, J. L.; Williams, K. H.; Maher, K.

2016-12-01

Dissolved organic carbon (DOC) is a critical chemical attribute of freshwater systems, affecting nutrient availability, toxicity and solubility of metals, and biological activity via the absorption of light and microbial consumption of O2 during DOC mineralization. Although DOC contributions to streams are distributed across the landscape in the shallow subsurface, many studies have demonstrated area-outsized contributions from riparian zones with high biological productivity and low subsurface O2 concentrations. In the East River, CO, a high-elevation watershed located in the central Rocky Mountains, initial observations show that DOC concentrations of two tributaries, Rock Creek and Gothic Creek, are elevated by 3-10 times compared to concentrations in the main East River and its other tributaries. These elevated concentrations are qualitatively linked to the unique presence of large wetlands in the headwaters of Rock and Gothic creeks, which due to potential anoxic conditions, experience reduced rates of organic matter decomposition and serve as an elevated source of DOC. In this study we quantify the cycling of organic matter in these alpine wetlands and their area-outsized contributions to East River DOC fluxes. We present concentration profiles of DOC along stream reaches and along subsurface flowpaths that span the transition from hillslope to wetland coupled with high-resolution mapping of chronically-saturated zones and calculate area-weighted fluxes of DOC from wetlands to Rock and Gothic creeks at multiple times through the 2016 growing season. Additionally, soil and groundwater DOC fluxes are compared with depth-resolved organic carbon content from soil cores, substrate quality (C:N), and soil surface CO2 fluxes to evaluate organic carbon budgets in the hillslope and wetland areas feeding Rock Creek. The characterization of these hotspots of DOC generation and transport in the East River is vital to the ability to predict nutrient cycling changes into the future.

Organic Carbon Mobilisation Mechanisms: Evidence from Globally Distributed Stalagmite Records

NASA Astrophysics Data System (ADS)

Baldini, J. U. L.; Fairchild, I. J.; Wynn, P.; Bourdin, C.; Muller, W.; Hartland, A.; Perrette, Y.; Worrall, F.; Bartlett, R.

2017-12-01

Identifying the cause of widespread increases in surface water dissolved organic carbon (DOC) concentrations in recent years is the subject of a contentious debate. Although DOC trends may partially reflect climate change, in many catchments they may also result from increased soil carbon solubility associated with decreases in acid rain due to lower atmospheric sulphur emissions. However, the lack of long-term DOC records hampers constraining climate's role in modulating DOC trends versus that of recovery from acidification. Here we help clarify the causes of recent DOC increases by using a combination of laboratory soil experiments and new stalagmite geochemical data. Laboratory experiments with soils sampled from above several key caves simulate the effect of acidity, temperature, and soil microbial processes on DOC release. These experiments are used to inform records of DOC encoded within several stalagmites from currently acidified, previously acidified, and unacidified sites, and which collectively yield insights into the timing of DOC change in the past. These records of stalagmite DOC concentration and composition are discussed within the context of the ongoing debate regarding the mechanism responsible for DOC release.

Linking CDOM spectral absorption to dissolved organic carbon concentrations and loadings in boreal estuaries

NASA Astrophysics Data System (ADS)

Asmala, Eero; Stedmon, Colin A.; Thomas, David N.

2012-10-01

The quantity of chromophoric dissolved organic matter (CDOM) and dissolved organic carbon (DOC) in three Finnish estuaries (Karjaanjoki, Kyrönjoki and Kiiminkijoki) was investigated, with respect to predicting DOC concentrations and loadings from spectral CDOM absorption measurements. Altogether 87 samples were collected from three estuarine transects which were studied in three seasons, covering a salinity range between 0 and 6.8, and DOC concentrations from 1572 μmol l-1 in freshwater to 222 μmol l-1 in coastal waters. CDOM absorption coefficient, aCDOM(375) values followed the trend in DOC concentrations across the salinity gradient and ranged from 1.67 to 33.4 m-1. The link between DOC and CDOM was studied using a range of wavelengths and algorithms. Wavelengths between 250 and 270 nm gave the best predictions with single linear regression. Total dissolved iron was found to influence the prediction in wavelengths above 520 nm. Despite significant seasonal and spatial differences in DOC-CDOM models, a universal relationship was tested with an independent data set and found to be robust. DOC and CDOM yields (loading/catchment area) from the catchments ranged from 1.98 to 5.44 g C m-2 yr-1, and 1.67 to 11.5 aCDOM(375) yr-1, respectively.

Mercury cycling in stream ecosystems. 2. Benthic methylmercury production and bed sediment - Pore water partitioning

USGS Publications Warehouse

Marvin-DiPasquale, Mark; Lutz, Michelle A; Brigham, Mark E.; Krabbenhoft, David P.; Aiken, George R.; Orem, William H.; Hall, Britt D.

2009-01-01

Mercury speciation, controls on methylmercury (MeHg) production, and bed sediment−pore water partitioning of total Hg (THg) and MeHg were examined in bed sediment from eight geochemically diverse streams where atmospheric deposition was the predominant Hg input. Across all streams, sediment THg concentrations were best described as a combined function of sediment percent fines (%fines; particles < 63 μm) and organic content. MeHg concentrations were best described as a combined function of organic content and the activity of the Hg(II)-methylating microbial community and were comparable to MeHg concentrations in streams with Hg inputs from industrial and mining sources. Whole sediment tin-reducible inorganic reactive Hg (Hg(II)R) was used as a proxy measure for the Hg(II) pool available for microbial methylation. In conjunction with radiotracer-derived rate constants of 203Hg(II) methylation, Hg(II)R was used to calculate MeHg production potential rates and to explain the spatial variability in MeHg concentration. The %Hg(II)R (of THg) was low (2.1 ± 5.7%) and was inversely related to both microbial sulfate reduction rates and sediment total reduced sulfur concentration. While sediment THg concentrations were higher in urban streams, %MeHg and %Hg(II)R were higher in nonurban streams. Sediment pore water distribution coefficients (log Kd’s) for both THg and MeHg were inversely related to the log-transformed ratio of pore water dissolved organic carbon (DOC) to bed sediment %fines. The stream with the highest drainage basin wetland density also had the highest pore water DOC concentration and the lowest log Kd’s for both THg and MeHg. No significant relationship existed between overlying water MeHg concentrations and those in bed sediment or pore water, suggesting upstream sources of MeHg production may be more important than local streambed production as a driver of water column MeHg concentration in drainage basins that receive Hg inputs primarily from atmospheric sources.

Declines in the dissolved organic carbon (DOC) concentration and flux from the UK

NASA Astrophysics Data System (ADS)

Worrall, Fred; Howden, Nicholas J. K.; Burt, Tim P.; Bartlett, Rebecca

2018-01-01

Increased concentrations of dissolved organic carbon (DOC) have been reported for many catchments across the northern hemisphere. Hypotheses to explain the increase have varied (eg. increasing air temperature or recovery from acidification) but one test of alternative hypotheses is the trend over the recent decade, with the competing hypotheses predicting: continuing increase; the rate of increase declining with time; and even decrease in concentration. In this study, records of DOC concentration in non-tidal rivers across the UK were examined for the period 2003-2012. The study found that: Of the 62 decade-long concentration trends that could be examined, 3 showed a significant increase, 17 experienced no significant change and 42 showed a significant decrease; in 28 of the 42 significant decreases, a significant step change was apparent with step changes being a decrease in concentration in every case. Of the 118 sites where annual flux and concentration records were available from 1974, 28 showed a significant step change down in flux and 52 showed a step down in concentration. The modal year of the step changes was 2000 with no step changes observed before 1982. At the UK national scale, DOC flux peaked in 2005 at 1354 ktonnes C/yr (5.55 tonnes C/km2/yr) but has declined since. The study suggests that there is a disconnection between DOC records from large catchments at their tidal limits and complementary records from headwater catchments, which means that mechanisms believed to be driving increases in DOC concentrations in headwaters will not necessarily be those controlling trends in DOC concentration further downstream. We propose that the changes identified here have been driven by changes in in-stream processing and changes brought about by the Urban Waste Water Treatment Directive. Therefore, signals identified in headwater catchments may bear little relation to those observed in large rivers much further downstream and vice versa.

Constraining the sources and cycling of dissolved organic carbon in a large oligotrophic lake using radiocarbon analyses

NASA Astrophysics Data System (ADS)

Zigah, Prosper K.; Minor, Elizabeth C.; McNichol, Ann P.; Xu, Li; Werne, Josef P.

2017-07-01

We measured the concentrations and isotopic compositions of solid phase extracted (SPE) dissolved organic carbon (DOC) and high molecular weight (HMW) DOC and their constituent organic components in order to better constrain the sources and cycling of DOC in a large oligotrophic lacustrine system (Lake Superior, North America). SPE DOC constituted a significant proportion (41-71%) of the lake DOC relative to HMW DOC (10-13%). Substantial contribution of 14C-depleted components to both SPE DOC (Δ14C = 25-43‰) and HMW DOC (Δ14C = 22-32‰) was evident during spring mixing, and depressed their radiocarbon values relative to the lake dissolved inorganic carbon (DIC; Δ14C ∼ 59‰). There was preferential removal of 14C-depleted (older) and thermally recalcitrant components from HMW DOC and SPE DOC in the summer. Contemporary photoautotrophic addition to HMW DOC was observed during summer stratification in contrast to SPE DOC, which decreased in concentration during stratification. Serial thermal oxidation radiocarbon analysis revealed a diversity of sources (both contemporary and older) within the SPE DOC, and also showed distinct components within the HMW DOC. The thermally labile components of HMW DOC were 14C-enriched and are attributed to heteropolysaccharides (HPS), peptides/amide and amino sugars (AMS) relative to the thermally recalcitrant components reflecting the presence of older material, perhaps carboxylic-rich alicyclic molecules (CRAM). The solvent extractable lipid-like fraction of HMW DOC was very 14C-depleted (as old as 1270-2320 14C years) relative to the carbohydrate-like and protein-like substances isolated by acid hydrolysis of HMW DOC. Our data constrain relative influences of contemporary DOC and old DOC, and DOC cycling in a modern freshwater ecosystem.

Spatiotemporal Variation of Dissolved Carbon in Semi-humid/arid Inland Waters: A Case Study from Songnen Plain, China

NASA Astrophysics Data System (ADS)

Song, K.; Li, L.; Zang, S.; Zhao, Y.

2012-12-01

Spatial and seasonal variations of dissolved organic carbon (DOC) and inorganic carbon (DIC) in 34 waters across the semi-humid/arid Songnen Plain, China were examined with 320 samples collected in 2011-2012. Large variations in both the concentration and quality of DOC are revealed, ranging from 0.47 mgL-1 to 720 mgL-1, which is mainly caused by the hydro-climatic condition in the plain. Large variations of DOC and DIC concentrations are observed between open (mean ± sd: 5.6 ± 2.4 mgL-1, 57.4 ± 34.7 mgL-1) and closed lakes (43.3 ± 7.9 mgL-1, 172.9 ± 113.3 mgL-1). Temporally, higher DOC and DIC concentrations are measured for ice-underlying water in winter than ice-free seasons. Colored dissolved organic matter (CDOM) and DOC concentrations are higher after high discharge events with terrigenous sources of CDOM/DOC dominated, while autochthonous sources also contributed to CDOM/DOC concentrations during algal bloom seasons. An interesting result of this study is that the non-outflow conditions for various water catchments had condensed effects on the dissolved carbon, resulting in close relationships between salinity and dissolved carbon parameters, e.g. salinity vs DOC (R2 = 0.83, p < 0.001), DIC (R2 = 0.96, p < 0.0001) using data set collected in 2011. Independent data set collected in May 2012 also confirmed this finding, yielding high correlation for salinity vs DOC (R2 = 0.79, p < 0.001), salinity vs DIC (R2 = 0.91, p < 0.0001), highlighting the potential of quantifying DOC/DIC from salinity measurements for thousand of waters dispersed in the semi-arid Songnen Plain. Indices based on CDOM absorption spectra, e.g. E250:365, DOC specific CDOM absorption (SUVA254) and spectral slope ratio (Sr, S275-295/S350-400), were applied to characterize DOM components and sources. Our results indicate high molecular weight CDOM fractions are more abundant in open waters than closed waters.

Atmospheric deposition as a source of carbon and nutrients to an alpine catchment of the Colorado Rocky Mountains

NASA Astrophysics Data System (ADS)

Mladenov, N.; Williams, M. W.; Schmidt, S. K.; Cawley, K.

2012-08-01

Many alpine areas are experiencing deglaciation, biogeochemical changes driven by temperature rise, and changes in atmospheric deposition. There is mounting evidence that the water quality of alpine streams may be related to these changes, including rising atmospheric deposition of carbon (C) and nutrients. Given that barren alpine soils can be severely C limited, atmospheric deposition sources may be an important source of C and nutrients for these environments. We evaluated the magnitude of atmospheric deposition of C and nutrients to an alpine site, the Green Lake 4 catchment in the Colorado Rocky Mountains. Using a long-term dataset (2002-2010) of weekly atmospheric wet deposition and snowpack chemistry, we found that volume weighted mean dissolved organic carbon (DOC) concentrations were 1.12 ± 0.19 mg l-1, and weekly concentrations reached peaks as high at 6-10 mg l-1 every summer. Total dissolved nitrogen concentration also peaked in the summer, whereas total dissolved phosphorus and calcium concentrations were highest in the spring. To investigate potential sources of C in atmospheric deposition, we evaluated the chemical quality of dissolved organic matter (DOM) and relationships between DOM and other solutes in wet deposition. Relationships between DOC concentration, fluorescence, and nitrate and sulfate concentrations suggest that pollutants from nearby urban and agricultural sources and organic aerosols derived from sub-alpine vegetation may influence high summer DOC wet deposition concentrations. Interestingly, high DOC concentrations were also recorded during "dust-in-snow" events in the spring, which may reflect an association of DOM with dust. Detailed chemical and spectroscopic analyses conducted for samples collected in 2010 revealed that the DOM in many late spring and summer samples was less aromatic and polydisperse and of lower molecular weight than that of winter and fall samples. Our C budget estimates for the Green Lake 4 catchment illustrated that wet deposition (9.9 kg C ha-1 yr-1) and dry deposition (6.9 kg C ha-1 yr-1) were a combined input of approximately 17 kg C ha-1 yr-1, which could be as high as 24 kg C ha-1 yr-1 in high dust years. This atmospheric C input approached the C input from microbial autotrophic production in barren soils. Atmospheric wet and dry deposition also contributed 4.3 kg N ha-1 yr-1, 0.15 kg P ha-1 yr-1, and 2.7 kg Ca2+ ha-1 yr-1 to this alpine catchment.

Modeling nonlinear responses of DOC transport in boreal catchments in Sweden

NASA Astrophysics Data System (ADS)

Kasurinen, Ville; Alfredsen, Knut; Ojala, Anne; Pumpanen, Jukka; Weyhenmeyer, Gesa A.; Futter, Martyn N.; Laudon, Hjalmar; Berninger, Frank

2016-07-01

Stream water dissolved organic carbon (DOC) concentrations display high spatial and temporal variation in boreal catchments. Understanding and predicting these patterns is a challenge with great implications for water quality projections and carbon balance estimates. Although several biogeochemical models have been used to estimate stream water DOC dynamics, model biases common during both rain and snow melt-driven events. The parsimonious DOC-model, K-DOC, with 10 calibrated parameters, uses a nonlinear discharge and catchment water storage relationship including soil temperature dependencies of DOC release and consumption. K-DOC was used to estimate the stream water DOC concentrations over 5 years for eighteen nested boreal catchments having total area of 68 km2 (varying from 0.04 to 67.9 km2). The model successfully simulated DOC concentrations during base flow conditions, as well as, hydrological events in catchments dominated by organic and mineral soils reaching NSEs from 0.46 to 0.76. Our semimechanistic model was parsimonious enough to have all parameters estimated using statistical methods. We did not find any clear differences between forest and mire-dominated catchments that could be explained by soil type or tree species composition. However, parameters controlling slow release and consumption of DOC from soil water behaved differently for small headwater catchments (less than 2 km2) than for those that integrate larger areas of different ecosystem types (10-68 km2). Our results emphasize that it is important to account for nonlinear dependencies of both, soil temperature, and catchment water storage, when simulating DOC dynamics of boreal catchments.

Abundance and patterns of transparent exopolymer particles (TEP) in Arctic floodplain lakes of the Mackenzie River Delta

NASA Astrophysics Data System (ADS)

Chateauvert, C. Adam; Lesack, Lance F. W.; Bothwell, Max L.

2012-12-01

The Mackenzie River Delta is a lake-rich arctic floodplain that receives high inputs of dissolved organic matter (DOM) and suspended particulates from allochthonous and autochthonous sources, and may transfer carbon from dissolved to particulate phase via in situ formation of transparent exopolymer particles (TEP). TEP provides food for grazers, surfaces for bacteria, and increased potential for aggregation and sedimentation of organic matter. During open water 2006, we tracked TEP abundances in three Delta lakes representing gradients that include declining river-to-lake connection times, increasing levels of dissolved organic carbon (DOC), and declining chromophoric-DOM (CDOM). Unexpectedly, TEP abundances were highest immediately after the flood, when autochthonous autotrophic production was at a seasonal low and CDOM a seasonal high. Moreover, the lake with the strongest riverine influence and lowest levels of autochthonous autotrophic production had the highest mean TEP-carbon (TEP-C) concentrations among the lakes. The mean proportion of particulate organic carbon (POC) represented by TEP-C increased with increasing river connection time, and appears to represent a substantial proportion of POC in Mackenzie Delta Lakes. Unexpectedly, the TEP gradient was most strongly related to CDOM (river water source) rather than overall DOC. Variations in CDOM accounted for 53% of TEP-C variation among the lakes, indicating allochthonous matter was the most important source of TEP. DOC release from in situ macrophytes during periods of high photosynthesis may contribute to TEP formation in the lake with lowest riverine influence, but pH levels >9.5 driven by the high photosynthetic rates complicate the interpretation of results from this lake.

[Influence of land use change on dissolved organic carbon export in Naoli River watershed. Northeast China].

PubMed

Yin, Xiao-min; Lyu, Xian-guo; Liu, Xing-tu; Xue, Zhen-shan

2015-12-01

The present study was conducted to evaluate the influence of land use change on dissolved organic carbon (DOC) export in Naoli River watershed, Northeast China. Seasonal variation of DOC concentrations of the river water and its relationship with land use in the whole watershed and 100 m riparian zone at the annual average scale were analyzed using the method of field sampling, laboratory analysis, GIS and statistics analysis. The results showed that the concentrations of DOC under base flow conditions in spring and summer were significantly higher than that in fall in the study watershed. The seasonal trend of DOC concentrations in wetland-watersheds was similar to that in all the sub-watersheds, while significantly different from that in non-wetland watersheds. On the annual average scale, percentage of wetland in the whole watershed and paddy field in the 100 m riparian zone had positive relationship with the DOC concentration in the river water, while percentage of forest in the whole watershed had negative relationship with it (P < 0.05). It indicated that wetland in the sub-watershed played a significant role in the seasonal variation of DOC in river water of Naoli River watershed. Wetland in the watershed and paddy field in the 100 m riparian zone significantly promoted DOC export, while forest alleviated it. Land use change in the watershed in the past few decades dramatically changed the DOC balance of river water.

Dissolved Organic Carbon Degradation in Response to Nutrient Amendments in Southwest Greenland Lakes

NASA Astrophysics Data System (ADS)

Burpee, B. T.; Northington, R.; Simon, K. S.; Saros, J. E.

2014-12-01

Aquatic ecosystems across the Arctic are currently experiencing rapid shifts in biotic, chemical, and physical factors in response to climate change. Preliminary data from multiple lakes in southwestern Greenland indicate decreasing dissolved organic carbon (DOC) concentrations over the past decade. Though several factors may be contributing to this phenomenon, this study attempts to elucidate the potential of heterotrophic bacteria to degrade DOC in the presence of increasing nutrient concentrations. In certain Arctic regions, nutrient subsidies have been released into lakes due to permafrost thaw. If this is occurring in southwestern Greenland, we hypothesized that increased nutrient concentrations will relieve nutrient limitation, thereby allowing heterotrophic bacteria to utilize DOC as an energy source. This prediction was tested using experimental DOC degradation assays from four sample lakes. Four nutrient amendment treatments (control, N, P, and N + P) were used to simulate in situ subsidies. Five time points were sampled during the incubation: days 0, 3, 6, 14, and 60. Total organic carbon (TOC) and parallel factor (PARAFAC) analysis were used to monitor the relative concentrations of different DOC fractions over time. In addition, samples for extracellular enzyme activity (EEA) analysis were collected at every time point. Early analysis of fulvic and humic pools of DOC do not indicate any significant change from days 0 to 14. This could be due to the fact that these DOC fractions are relatively recalcitrant. This study will be important in determining whether bacterial degradation could be a contributing factor to DOC decline in arctic lakes.

Variation in fish mercury concentrations in streams of the Adirondack region, New York: A simplified screening approach using chemical metrics

USGS Publications Warehouse

Burns, Douglas A.; Riva-Murray, Karen

2018-01-01

Simple screening approaches for the neurotoxicant methylmercury (MeHg) in aquatic ecosystems may be helpful in risk assessments of natural resources. We explored the development of such an approach in the Adirondack Mountains of New York, USA, a region with high levels of MeHg bioaccumulation. Thirty-six perennial streams broadly representative of 1st and 2nd order streams in the region were sampled during summer low flow and analyzed for several solutes and for Hg concentrations in fish. Several landscape and chemical metrics that are typically strongly related to MeHg concentrations in aquatic biota were explored for strength of association with fish Hg concentrations. Data analyses were based on site mean length-normalized and standardized Hg concentrations (assumed to be dominantly MeHg) in whole juvenile and adult Brook Trout Salvelinus fontinalis, Creek Chub Semotilus atromaculatus, Blacknose Dace Rhinichthys atratulus, and Central Mudminnow Umbra limi, as well as on multi-species z-scores. Surprisingly, none of the landscape metrics was related significantly to regional variation in fish Hg concentrations or to z-scores across the study streams. In contrast, several chemical metrics including dissolved organic carbon (DOC) concentrations, sulfate concentrations (SO42−), pH, ultra-violet absorbance (UV254), and specific ultra-violet absorbance were significantly related to regional variation in fish Hg concentrations. A cluster analysis based on DOC, SO42−, and pH identified three distinct groups of streams: (1) high DOC, acidic streams, (2) moderate DOC, slightly acidic streams, and (3) low DOC circum-neutral streams with relatively high SO42−. Preliminary analysis indicated no significant difference in fish Hg z-scores between the moderate and high DOC groups, so these were combined for further analysis. The resulting two groups showed strong differences (p < 0.001) in DOC and SO42−concentrations as well as in pH and UV254 values. Median fish z-scores were significantly higher (p = 0.002) in the group of streams with higher DOC and UV254 and lower pH and SO42−. Screening values of DOC >6.9 mg/L, SO42− <2.8 mg/L, pH <6.6, and UV254>0.31 cm−1 were tested as thresholds to identify Adirondack stream sites likely to have higher fish Hg concentrations. By applying a combined threshold of exceedance for either pH or UV254, sites with fish Hg concentrations that exceeded a wildlife guideline of 100 ng/g were correctly identified about 75% of the time among the 36 study streams. An estimate of Hg risk applied to a data set of 391 streams based on DOC concentrations showed that about 28% were likely to pose high risk to wildlife; most of these streams were located in the western Adirondacks.

Influences of organic carbon speciation on hyporheic corridor biogeochemistry and microbial ecology.

PubMed

Stegen, James C; Johnson, Tim; Fredrickson, James K; Wilkins, Michael J; Konopka, Allan E; Nelson, William C; Arntzen, Evan V; Chrisler, William B; Chu, Rosalie K; Fansler, Sarah J; Graham, Emily B; Kennedy, David W; Resch, Charles T; Tfaily, Malak; Zachara, John

2018-02-08

The hyporheic corridor (HC) encompasses the river-groundwater continuum, where the mixing of groundwater (GW) with river water (RW) in the HC can stimulate biogeochemical activity. Here we propose a novel thermodynamic mechanism underlying this phenomenon and reveal broader impacts on dissolved organic carbon (DOC) and microbial ecology. We show that thermodynamically favorable DOC accumulates in GW despite lower DOC concentration, and that RW contains thermodynamically less-favorable DOC, but at higher concentrations. This indicates that GW DOC is protected from microbial oxidation by low total energy within the DOC pool, whereas RW DOC is protected by lower thermodynamic favorability of carbon species. We propose that GW-RW mixing overcomes these protections and stimulates respiration. Mixing models coupled with geophysical and molecular analyses further reveal tipping points in spatiotemporal dynamics of DOC and indicate important hydrology-biochemistry-microbial feedbacks. Previously unrecognized thermodynamic mechanisms regulated by GW-RW mixing may therefore strongly influence biogeochemical and microbial dynamics in riverine ecosystems.

Concentration, sources, and flux of dissolved organic carbon of precipitation at Lhasa city, the Tibetan Plateau.

PubMed

Li, Chaoliu; Yan, Fangping; Kang, Shichang; Chen, Pengfei; Qu, Bin; Hu, Zhaofu; Sillanpää, Mika

2016-07-01

Dissolved organic carbon (DOC) plays an important role in the climate system, but few data are available on the Tibetan Plateau (TP). In this study, 89 precipitation samples were collected at Lhasa, the largest city of southern Tibet, from March to December 2013. The average concentration and wet deposition flux of DOC was 1.10 mg C L(-1) and 0.63 g C m(-2) year(-1), respectively. Seasonally, low DOC concentration and high flux appeared during the monsoon period, which were in line with heavy precipitation amount, reflecting dilution effect of precipitation for the DOC. Compared to other regions, the values of Lhasa were lower than those of large cities (e.g., Beijing and Seoul) mainly because of less air pollution of Lhasa. The principal component analysis (PCA) of DOC and ions (Ca(2+), Mg(2+), Na(+), K(+), NH4 (+), Cl(-), NO3 (-), and SO4 (2-)) showed that DOC of Lhasa was derived mainly from the natural sources, followed by anthropogenic burning activities. Furthermore, △(14)C value of DOC indicated that fossil fuel combustion contributed around 28 % of the rainwater DOC of Lhasa, indicating that the atmosphere of Lhasa has been influenced by emission from fossil fuel combustion or high-temperature industrial processes.

Distribution of trace metals in anchialine caves of Adriatic Sea, Croatia

NASA Astrophysics Data System (ADS)

Cuculić, Vlado; Cukrov, Neven; Kwokal, Željko; Mlakar, Marina

2011-11-01

This study presents results of the first comprehensive research on ecotoxic trace metals (Cd, Pb, Cu and Zn) in aquatic anchialine ecosystems. Data show the influence of hydrological and geological characteristics on trace metals in highly stratified anchialine water columns. Distribution of Cd, Pb, Cu and Zn in two anchialine water bodies, Bjejajka Cave and Lenga Pit in the Mljet National park, Croatia were investigated seasonally from 2006 to 2010. Behaviour and concentrations of dissolved and total trace metals in stratified water columns and metal contents in sediment, carbonate rocks and soil of the anchialine environment were evaluated. Trace metals and dissolved organic carbon (DOC) concentrations in both anchialine water columns were significantly elevated compared to adjacent seawater. Zn and Cu concentrations were the highest in the Lenga Pit water column and sediment. Elevated concentrations of Zn, Pb and Cu in Bjejajka Cave were mainly terrigenous. Significantly elevated concentrations of cadmium (up to 0.3 μg L -1) were found in the water column of Bjejajka cave, almost two orders of magnitude higher compared to nearby surface seawater. Laboratory analysis revealed that bat guano was the major source of cadmium in Bjejajka Cave. Cadmium levels in Lenga Pit, which lacks accumulations of bat guano, were 20-fold lower. Moreover, low metal amounts in carbonate rocks in both caves, combined with mineral leaching experiments, revealed that carbonates play a minor role as a source of metals in both water columns. We observed two types of vertical distribution pattern of cadmium in the stratified anchialine Bjejajka Cave water column. At lower salinities, non-conservative behaviour was characterized by strong desorption and enrichment of dissolved phase while, at salinities above 20, Cd behaved conservatively and its dissolved concentration decreased. Conservative behaviour of Cu, Pb, Zn and DOC was observed throughout the water column. After heavy rains, Cd showed reduced concentration and uniform vertical distribution, suggesting a non-terrestrial origin. Under the same conditions, concentrations of total and dissolved Pb, Cu, Zn and DOC were significantly elevated. Variations of trace metal vertical distributions in anchialine water columns were caused by large inputs of fresh water (extraordinary rainy events), and were not influenced by seasonal changes.

Landscape controls on mercury in streamwater at Acadia National Park, USA

USGS Publications Warehouse

Peckenham, J.M.; Kahl, J.S.; Nelson, S.J.; Johnson, K.B.; Haines, T.A.

2007-01-01

Fall and spring streamwater samples were analyzed for total mercury (Hg) and major ions from 47 locations on Mount Desert Island in Maine. Samples were collected in zones that were burned in a major wildfire in 1947 and in zones that were not burned. We hypothesized that Hg concentrations in streamwater would be higher from unburned sites than burned watersheds, because fire would volatilize stored Hg. The Hg concentrations, based on burn history, were not statistically distinct. However, significant statistical associations were noted between Hg and the amount of wetlands in the drainage systems and with streamwater dissolved organic carbon (DOC). An unexpected result was that wetlands mobilized more Hg by generating more DOC in total, but upland DOC was more efficient at transporting Hg because it transports more Hg per unit DOC. Mercury concentrations were higher in samples collected at lower elevations. Mercury was positively correlated with relative discharge, although this effect was not distinguished from the DOC association. In this research, sample site elevation and the presence of upstream wetlands and their associated DOC affected Hg concentrations more strongly than burn history. ?? Springer Science + Business Media B.V. 2007.

Bioavailable dissolved and particulate organic carbon flux from coastal temperate rainforest watersheds

NASA Astrophysics Data System (ADS)

Fellman, J.; Hood, E. W.; D'Amore, D. V.; Moll, A.

2017-12-01

Coastal temperate rainforest (CTR) watersheds of southeast Alaska have dense soil carbon stocks ( 300 Mg C ha-1) and high specific discharge (1.5-7 m yr-1) driven by frontal storms from the Gulf of Alaska. As a result, dissolved organic carbon (DOC) fluxes from Alaskan CTR watersheds are estimated to exceed 2 Tg yr-1; however, little is known about the export of particulate organic carbon (POC). The magnitude and bioavailability of this land-to-ocean flux of terrigenous organic matter ultimately determines how much metabolic energy is translocated to downstream and coastal marine ecosystems in this region. We sampled streamwater weekly from May through October from four watersheds of varying landcover (gradient of wetland to glacial coverage) to investigate changes in the concentration and flux of DOC and POC exported to the coastal ocean. We also used headspace analysis of CO2 following 14 day laboratory incubations to determine the flux of bioavailable DOC and POC exported from CTR watersheds. Across all sites, bioavailable DOC concentrations ranged from 0.2 to 1.9 mg L-1 but were on average 0.6 mg L-1. For POC, bioavailable concentrations ranged from below detection to 0.3 mg L-1 but were on average 0.1 mg L-1. The concentration, flux and bioavailability of DOC was higher than for POC highlighting the potential importance of DOC as a metabolic subsidy to downstream and coastal environments. Ratios of DOC to POC decreased during high flow events because the increase in POC concentrations with discharge exceeds that for DOC. Overall, our findings suggest that projected increases in precipitation and storm intensity will drive changes in the speciation, magnitude and bioavailability of the organic carbon flux from CTR watersheds.

Long-term patterns and short-term dynamics of stream solutes and suspended sediment in a rapidly weathering tropical watershed

NASA Astrophysics Data System (ADS)

Shanley, James B.; McDowell, William H.; Stallard, Robert F.

2011-07-01

The 326 ha Río Icacos watershed in the tropical wet forest of the Luquillo Mountains, northeastern Puerto Rico, is underlain by granodiorite bedrock with weathering rates among the highest in the world. We pooled stream chemistry and total suspended sediment (TSS) data sets from three discrete periods: 1983-1987, 1991-1997, and 2000-2008. During this period three major hurricanes crossed the site: Hugo in 1989, Hortense in 1996, and Georges in 1998. Stream chemistry reflects sea salt inputs (Na, Cl, and SO4), and high weathering rates of the granodiorite (Ca, Mg, Si, and alkalinity). During rainfall, stream composition shifts toward that of precipitation, diluting 90% or more in the largest storms, but maintains a biogeochemical watershed signal marked by elevated K and dissolved organic carbon (DOC) concentration. DOC exhibits an unusual "boomerang" pattern, initially increasing with flow but then decreasing at the highest flows as it becomes depleted and/or vigorous overland flow minimizes contact with watershed surfaces. TSS increased markedly with discharge (power function slope 1.54), reflecting the erosive power of large storms in a landslide-prone landscape. The relations of TSS and most solute concentrations with stream discharge were stable through time, suggesting minimal long-term effects from repeated hurricane disturbance. Nitrate concentration, however, increased about threefold in response to hurricanes then returned to baseline over several years following a pseudo first-order decay pattern. The combined data sets provide insight about important hydrologic pathways, a long-term perspective to assess response to hurricanes, and a framework to evaluate future climate change in tropical ecosystems.

Long-term patterns and short-term dynamics of stream solutes and suspended sediment in a rapidly weathering tropical watershed

USGS Publications Warehouse

Shanley, James B.; McDowell, William H.; Stallard, Robert F.

2011-01-01

The 326 ha Río Icacos watershed in the tropical wet forest of the Luquillo Mountains, northeastern Puerto Rico, is underlain by granodiorite bedrock with weathering rates among the highest in the world. We pooled stream chemistry and total suspended sediment (TSS) data sets from three discrete periods: 1983-1987, 1991-1997, and 2000-2008. During this period three major hurricanes crossed the site: Hugo in 1989, Hortense in 1996, and Georges in 1998. Stream chemistry reflects sea salt inputs (Na, Cl, and SO4), and high weathering rates of the granodiorite (Ca, Mg, Si, and alkalinity). During rainfall, stream composition shifts toward that of precipitation, diluting 90% or more in the largest storms, but maintains a biogeochemical watershed signal marked by elevated K and dissolved organic carbon (DOC) concentration. DOC exhibits an unusual "boomerang" pattern, initially increasing with flow but then decreasing at the highest flows as it becomes depleted and/or vigorous overland flow minimizes contact with watershed surfaces. TSS increased markedly with discharge (power function slope 1.54), reflecting the erosive power of large storms in a landslide-prone landscape. The relations of TSS and most solute concentrations with stream discharge were stable through time, suggesting minimal long-term effects from repeated hurricane disturbance. Nitrate concentration, however, increased about threefold in response to hurricanes then returned to baseline over several years following a pseudo first-order decay pattern. The combined data sets provide insight about important hydrologic pathways, a long-term perspective to assess response to hurricanes, and a framework to evaluate future climate change in tropical ecosystems.

Long-term patterns and short-term dynamics of stream solutes and suspended sediment in a rapidly weathering tropical watershed

USGS Publications Warehouse

Shanley, J.B.; McDowell, W.H.; Stallard, R.F.

2011-01-01

The 326 ha R??o Icacos watershed in the tropical wet forest of the Luquillo Mountains, northeastern Puerto Rico, is underlain by granodiorite bedrock with weathering rates among the highest in the world. We pooled stream chemistry and total suspended sediment (TSS) data sets from three discrete periods: 1983-1987, 1991-1997, and 2000-2008. During this period three major hurricanes crossed the site: Hugo in 1989, Hortense in 1996, and Georges in 1998. Stream chemistry reflects sea salt inputs (Na, Cl, and SO4), and high weathering rates of the granodiorite (Ca, Mg, Si, and alkalinity). During rainfall, stream composition shifts toward that of precipitation, diluting 90% or more in the largest storms, but maintains a biogeochemical watershed signal marked by elevated K and dissolved organic carbon (DOC) concentration. DOC exhibits an unusual "boomerang" pattern, initially increasing with flow but then decreasing at the highest flows as it becomes depleted and/or vigorous overland flow minimizes contact with watershed surfaces. TSS increased markedly with discharge (power function slope 1.54), reflecting the erosive power of large storms in a landslide-prone landscape. The relations of TSS and most solute concentrations with stream discharge were stable through time, suggesting minimal long-term effects from repeated hurricane disturbance. Nitrate concentration, however, increased about threefold in response to hurricanes then returned to baseline over several years following a pseudo first-order decay pattern. The combined data sets provide insight about important hydrologic pathways, a long-term perspective to assess response to hurricanes, and a framework to evaluate future climate change in tropical ecosystems. Copyright 2011 by the American Geophysical Union.

Estimating dissolved organic carbon concentration in turbid coastal waters using optical remote sensing observations

NASA Astrophysics Data System (ADS)

Cherukuru, Nagur; Ford, Phillip W.; Matear, Richard J.; Oubelkheir, Kadija; Clementson, Lesley A.; Suber, Ken; Steven, Andrew D. L.

2016-10-01

Dissolved Organic Carbon (DOC) is an important component in the global carbon cycle. It also plays an important role in influencing the coastal ocean biogeochemical (BGC) cycles and light environment. Studies focussing on DOC dynamics in coastal waters are data constrained due to the high costs associated with in situ water sampling campaigns. Satellite optical remote sensing has the potential to provide continuous, cost-effective DOC estimates. In this study we used a bio-optics dataset collected in turbid coastal waters of Moreton Bay (MB), Australia, during 2011 to develop a remote sensing algorithm to estimate DOC. This dataset includes data from flood and non-flood conditions. In MB, DOC concentration varied over a wide range (20-520 μM C) and had a good correlation (R2 = 0.78) with absorption due to coloured dissolved organic matter (CDOM) and remote sensing reflectance. Using this data set we developed an empirical algorithm to derive DOC concentrations from the ratio of Rrs(412)/Rrs(488) and tested it with independent datasets. In this study, we demonstrate the ability to estimate DOC using remotely sensed optical observations in turbid coastal waters.

[Estimation of DOC concentrations using CDOM absorption coefficients: a case study in Taihu Lake].

PubMed

Jiang, Guang-Jia; Ma, Rong-Hua; Duan, Hong-Tao

2012-07-01

Dissolved organic carbon (DOC) is the largest organic carbon stock in water ecosystems, which plays an important role in the carbon cycle in water. Chromophoric dissolved organic matter (CDOM), an important water color variation, is the colored fraction of DOC and its absorption controls the instruction of light under water. The available linkage between DOC concentration and CDOM absorptions enables the determination of DOC accumulations using remote sensing reflectance or radiance in lake waters. The present study explored the multi-liner relationship between CDOM absorptions [a(g) (250) and a(g) (365)] and DOC concentrations in Taihu Lake, based on the available data in 4 cruises (201005, 201101, 201103, 201105) (totally 183 sampling sites). Meanwhile, the results were validated with the data of the experiment carried out from August 29 to September 2, 2011 in Taihu Lake (n = 27). Furthermore, a universal pattern of modeling from remote sensing was built for lake waters. The results demonstrated that this method provided more satisfying estimation of DOC concentrations in Taihu Lake. Except the data obtained in January 2011, the fitted results of which were not conductive to the winter dataset (201101) in Taihu Lake, due to the diverse sources and sinks of DOC and CDOM, the multi-liner relationship was robust for the data collected in the other three cruises (R2 = 0.64, RMSE = 14.31%, n = 164), which was validated using the 201108 sampling dataset (R2 = 0.67, RMSE = 10.58%, n = 27). In addition, the form of the statistic model is universal, to some extent, for other water areas, however, there is difference in the modeling coefficients. Further research should be focused on the parameterization using local data from different lakes, which provides effective methodology for the estimation of DOC concentrations in lakes and other water regions.

Impact of organic carbon and nutrients mobilized during chemical oxidation on subsequent bioremediation of a diesel-contaminated soil.

PubMed

Sutton, Nora B; Grotenhuis, Tim; Rijnaarts, Huub H M

2014-02-01

Remediation with in situ chemical oxidation (ISCO) impacts soil organic matter (SOM) and the microbial community, with deleterious effects on the latter being a major hurdle to coupling ISCO with in situ bioremediation (ISB). We investigate treatment of a diesel-contaminated soil with Fenton's reagent and modified Fenton's reagent coupled with a subsequent bioremediation phase of 187d, both with and without nutrient amendment. Chemical oxidation mobilized SOM into the liquid phase, producing dissolved organic carbon (DOC) concentrations 8-16 times higher than the untreated field sample. Higher aqueous concentrations of nitrogen and phosphorous species were also observed following oxidation; NH4(+) increased 14-172 times. During the bioremediation phase, dissolved carbon and nutrient species were utilized for microbial growth-yielding DOC concentrations similar to field sample levels within 56d of incubation. In the absence of nutrient amendment, the highest microbial respiration rates were correlated with higher availability of nitrogen and phosphorus species mobilized by oxidation. Significant diesel degradation was only observed following nutrient amendment, implying that nutrients mobilized by chemical oxidation can increase microbial activity but are insufficient for bioremediation. While all bioremediation occurred in the first 28d of incubation in the biotic control microcosm with nutrient amendment, biodegradation continued throughout 187d of incubation following chemical oxidation, suggesting that chemical treatment also affects the desorption of organic contaminants from SOM. Overall, results indicate that biodegradation of DOC, as an alternative substrate to diesel, and biological utilization of mobilized nutrients have implications for the success of coupled ISCO and ISB treatments. Copyright © 2013 Elsevier Ltd. All rights reserved.

Identification and analysis of low-molecular-weight dissolved organic carbon in subglacial basal ice ecosystems by ion chromatography

NASA Astrophysics Data System (ADS)

O'Donnell, Emily C.; Wadham, Jemma L.; Lis, Grzegorz P.; Tranter, Martyn; Pickard, Amy E.; Stibal, Marek; Dewsbury, Paul; Fitzsimons, Sean

2016-07-01

Determining the concentration and composition of dissolved organic carbon (DOC) in glacial ecosystems is important for assessments of in situ microbial activity and contributions to wider biogeochemical cycles. Nonetheless, there is limited knowledge of the abundance and character of DOC in basal ice and the subglacial environment and a lack of quantitative data on low-molecular-weight (LMW) DOC components, which are believed to be highly bioavailable to microorganisms. We investigated the abundance and composition of DOC in basal ice via a molecular-level DOC analysis. Spectrofluorometry and a novel ion chromatographic method, which has been little utilized in glacial science for LMW-DOC determinations, were employed to identify and quantify the major LMW fractions (free amino acids, carbohydrates, and carboxylic acids) in basal ice from four glaciers, each with a different type of overridden material (i.e. the pre-entrainment sedimentary type such as lacustrine material or palaeosols). Basal ice from Joyce Glacier (Antarctica) was unique in that 98 % of the LMW-DOC was derived from the extremely diverse free amino acid (FAA) pool, comprising 14 FAAs. LMW-DOC concentrations in basal ice were dependent on the bioavailability of the overridden organic carbon (OC), which in turn was influenced by the type of overridden material. Mean LMW-DOC concentrations in basal ice from Russell Glacier (Greenland), Finsterwalderbreen (Svalbard), and Engabreen (Norway) were low (0-417 nM C), attributed to the relatively refractory nature of the OC in the overridden palaeosols and bedrock. In contrast, mean LMW-DOC concentrations were an order of magnitude higher (4430 nM C) in basal ice from Joyce Glacier, a reflection of the high bioavailability of the overridden lacustrine material (> 17 % of the sediment OC comprised extractable carbohydrates, a proxy for bioavailable OC). We find that the overridden material may act as a direct (via abiotic leaching) and indirect (via microbial cycling) source of DOC to the subglacial environment and provides a range of LMW-DOC compounds that may stimulate microbial activity in wet subglacial sediments.

Benthic fluxes of dissolved organic carbon from gas hydrate sediments in the northern South China Sea

PubMed Central

Hung, Chia-Wei; Huang, Kuo-Hao; Shih, Yung-Yen; Lin, Yu-Shih; Chen, Hsin-Hung; Wang, Chau-Chang; Ho, Chuang-Yi; Hung, Chin-Chang; Burdige, David J.

2016-01-01

Hydrocarbon vents have recently been reported to contribute considerable amounts of dissolved organic carbon (DOC) to the oceans. Many such hydrocarbon vents widely exist in the northern South China Sea (NSCS). To investigate if these hydrocarbon vent sites release DOC, we used a real-time video multiple-corer to collect bottom seawater and surface sediments at vent sites. We analyzed concentrations of DOC in these samples and estimated DOC fluxes. Elevated DOC concentrations in the porewaters were found at some sites suggesting that DOC may come from these hydrocarbon vents. Benthic fluxes of DOC from these sediments were 28 to 1264 μmol m−2 d−1 (on average ~321 μmol m−2 d−1) which are several times higher than most DOC fluxes in coastal and continental margin sediments. The results demonstrate that the real-time video multiple-corer can precisely collect samples at vent sites. The estimated benthic DOC flux from the methane venting sites (8.6 × 106 mol y−1), is 24% of the DOC discharge from the Pearl River to the South China Sea, indicating that these sediments make an important contribution to the DOC in deep waters. PMID:27432631

Geochemistry and Flux of Terrigenous Dissolved Organic Matter to the Arctic Ocean

NASA Astrophysics Data System (ADS)

Spencer, R. G.; Mann, P. J.; Hernes, P. J.; Tank, S. E.; Striegl, R. G.; Dyda, R. Y.; Peterson, B. J.; McClelland, J. W.; Holmes, R. M.

2011-12-01

Rivers draining into the Arctic Ocean exhibit high concentrations of terrigenous dissolved organic carbon (DOC) and recent studies indicate that DOC export is changing due to climatic warming and alteration in permafrost condition. The fate of exported DOC in the Arctic Ocean is of key importance for understanding the regional carbon cycle and remains a point of discussion in the literature. As part of the Arctic Great Rivers Observatory (Arctic-GRO) project, samples were collected for DOC, chromophoric dissolved organic matter (CDOM) and lignin phenols from the Ob', Yenisey, Lena, Kolyma, Mackenzie and Yukon rivers in 2009 - 2010. DOC and lignin concentrations were elevated during the spring freshet and measurements related to DOC composition indicated an increasing contribution from terrestrial vascular plant sources at this time of year (e.g. lignin carbon-normalized yield, CDOM spectral slope, SUVA254, humic-like fluorescence). CDOM absorption was found to correlate strongly with both DOC (r2=0.83) and lignin concentration (r2=0.92) across the major arctic rivers. Utilizing these relationships we modeled loads for DOC and lignin export from high-resolution CDOM measurements (daily across the freshet) to derive improved flux estimates, particularly from the dynamic spring discharge maxima period when the majority of DOC and lignin export occurs. The new load estimates for DOC and lignin are higher than previous evaluations, emphasizing that if these are more representative of current arctic riverine export, terrigenous DOC is transiting through the Arctic Ocean at a faster rate than previously thought. It is apparent that higher resolution sampling of arctic rivers is exceptionally valuable with respect to deriving accurate fluxes and we highlight the potential of CDOM in this role for future studies and the applicability of in-situ CDOM sensors.

Determining sources of dissolved organic carbon and disinfection byproduct precursors to the McKenzie River, Oregon

USGS Publications Warehouse

Kraus, Tamara E.C.; Anderson, Chauncey W.; Morgenstern, Karl; Downing, Bryan D.; Pellerin, Brian A.; Bergamaschi, Brian A.

2010-01-01

This study was conducted to determine the main sources of dissolved organic carbon (DOC) and disinfection byproduct (DBP) precursors to the McKenzie River, Oregon (USA). Water samples collected from the mainstem, tributaries, and reservoir outflows were analyzed for DOC concentration and DBP formation potentials (trihalomethanes [THMFPs] and haloacetic acids [HAAFPs]). In addition, optical properties (absorbance and fluorescence) of dissolved organic matter (DOM) were measured to provide insight into DOM composition and assess whether optical properties are useful proxies for DOC and DBP precursor concentrations. Optical properties indicative of composition suggest that DOM in the McKenzie River mainstem was primarily allochthonous - derived from soils and plant material in the upstream watershed. Downstream tributaries had higher DOC concentrations than mainstem sites (1.6 ?? 0.4 vs. 0.7 ?? 0.3 mg L-1) but comprised <5% of mainstem flows and had minimal effect on overall DBP precursor loads. Water exiting two large upstream reservoirs also had higher DOC concentrations than the mainstem site upstream of the reservoirs, but optical data did not support in situ algal production as a source of the added DOC during the study. Results suggest that the first major rain event in the fall contributes DOM with high DBP precursor content. Although there was interference in the absorbance spectra in downstream tributary samples, fluorescence data were strongly correlated to DOC concentration (R 2 = 0.98), THMFP (R2 = 0.98), and HAAFP (R2 = 0.96). These results highlight the value of using optical measurements for identifying the concentration and sources of DBP precursors in watersheds, which will help drinking water utilities improve source water monitoring and management programs. Copyright ?? 2010 by the American Society of Agronomy.

Vegetation and climate controls on potential CO2, DOC and DON production in northern latitude soils

USGS Publications Warehouse

Neff, J.C.; Hooper, D.U.

2002-01-01

Climatic change may influence decomposition dynamics in arctic and boreal ecosystems, affecting both atmospheric CO2 levels, and the flux of dissolved organic carbon (DOC) and dissolved organic nitrogen (DON) to aquatic systems. In this study, we investigated landscape-scale controls on potential production of these compounds using a one-year laboratory incubation at two temperatures (10?? and 30??C). We measured the release of CO2, DOC and DON from tundra soils collected from a variety of vegetation types and climatic regimes: tussock tundra at four sites along a latitudinal gradient from the interior to the north slope of Alaska, and soils from additional vegetation types at two of those sites (upland spruce at Fairbanks, and wet sedge and shrub tundra at Toolik Lake in northern Alaska). Vegetation type strongly influenced carbon fluxes. The highest CO2 and DOC release at the high incubation temperature occurred in the soils of shrub tundra communities. Tussock tundra soils exhibited the next highest DOC fluxes followed by spruce and wet sedge tundra soils, respectively. Of the fluxes, CO2 showed the greatest sensitivity to incubation temperatures and vegetation type, followed by DOC. DON fluxes were less variable. Total CO2 and total DOC release were positively correlated, with DOC fluxes approximately 10% of total CO2 fluxes. The ratio of CO2 production to DOC release varied significantly across vegetation types with Tussock soils producing an average of four times as much CO2 per unit DOC released compared to Spruce soils from the Fairbanks site. Sites in this study released 80-370 mg CO2-C g soil C-1 and 5-46 mg DOC g soil C-1 at high temperatures. The magnitude of these fluxes indicates that arctic carbon pools contain a large proportion of labile carbon that could be easily decomposed given optimal conditions. The size of this labile pool ranged between 9 and 41% of soil carbon on a g soil C basis, with most variation related to vegetation type rather than climate.

Sorption of the pharmaceuticals carbamazepine and naproxen to dissolved organic matter: role of structural fractions.

PubMed

Maoz, Adi; Chefetz, Benny

2010-02-01

Pharmaceutical compounds and dissolved organic matter (DOM) are co-introduced into the environment by irrigation with reclaimed wastewater and/or application of biosolids. In this study, we evaluate the role and mechanism of interaction of the pharmaceuticals naproxen and carbamazepine with structural fractions of biosolids-derived DOM. Sorption interactions were estimated from dialysis-bag experiments at different pHs. Sorption of naproxen and carbamazepine by the hydrophobic acid fraction exhibited strong pH-dependence. With both pharmaceuticals, the highest sorption coefficients (K(DOC)) were at pH 4. With the hydrophobic neutral fraction, pH affected only naproxen sorption (decreasing with increasing pH). Among the hydrophilic DOM fractions, the hydrophilic acid fraction exhibited the highest K(DOC) value for carbamazepine, probably due to their bipolar character. In the hydrophilic acid fraction-naproxen system, significant anionic repulsion was observed with increasing pH. The hydrophilic base fraction contains positively charged functional groups. Therefore with increasing ionization of naproxen (with increasing pH), K(DOC) to this fraction increased. The hydrophilic neutral fraction exhibited the lowest K(DOC) with both studied pharmaceuticals. The K(DOC) value of carbamazepine with the bulk DOM sample was higher than the calculated K(DOC) value based on sorption by the individual isolated fractions. The opposite trend was observed with naproxen at pH 8: the calculated K(DOC) value was higher than the value obtained for the bulk DOM. These results demonstrate that DOM fractions interact with each other and do not act as separate sorption domains. (c) 2009 Elsevier Ltd. All rights reserved.

Land management impacts on dairy-derived dissolved organic carbon in ground water

USGS Publications Warehouse

Chomycia, J.C.; Hernes, P.J.; Harter, T.; Bergamaschi, B.A.

2008-01-01

Dairy operations have the potential to elevate dissolved organic carbon (DOC) levels in ground water, where it may interact with organic and inorganic contaminants, fuel denitrification, and may present problems for drinking water treatment. Total and percent bioavailable DOC and total and carbon-specific trihalomethane (THM) formation potential (TTHMFP and STHMFP, respectively) were determined for shallow ground water samples from beneath a dairy farm in the San Joaquin Valley, California. Sixteen wells influenced by specific land management areas were sampled over 3 yr. Measured DOC concentrations were significantly elevated over the background as measured at an upgradient monitoring well, ranging from 13 to 55 mg L-1 in wells downgradient from wastewater ponds, 8 to 30 mg L-1 in corral wells, 5 to 12 mg L-1 in tile drains, and 4 to 15 mg L-1 in wells associated with manured fields. These DOC concentrations were at the upper range or greatly exceeded concentrations in most surface water bodies used as drinking water sources in California. DOC concentrations in individual wells varied by up to a factor of two over the duration of this study, indicating a dynamic system of sources and degradation. DOC bioavailability over 21 d ranged from 3 to 10%, comparable to surface water systems and demonstrating the potential for dairy-derived DOC to influence dissolved oxygen concentrations (nearly all wells were hypoxic to anoxic) and denitrification. TTHMFP measurements across all management units ranged from 141 to 1731 ??g L-1, well in excess of the maximum contaminant level of 80 ??g L-1 established by the Environmental Protection Agency. STHMFP measurements demonstrated over twofold variation (???4 to ???8 mmol total THM/mol DOC) across the management areas, indicating the dependence of reactivity on DOC composition. The results indicate that land management strongly controls the quantity and quality of DOC to reach shallow ground water and hence should be considered when managing ground water resources and in any efforts to mitigate contamination of ground water with carbon-based contaminants, such as pesticides and pharmaceuticals. Copyright ?? 2008 by the American Society of Agronomy, Crop Science Society of America, and Soil Science Society of America. All rights reserved.

Linking pulses of atmospheric deposition to DOC release in an upland peat-covered catchment

NASA Astrophysics Data System (ADS)

Worrall, F.; Burt, T. P.; Adamson, J. K.

2008-12-01

Changes in atmospheric deposition have been proposed as one possible explanation of the widespread increase in DOC concentration observed in many Northern Hemisphere catchments. This study uses detailed, long-term, monthly monitoring records of pH, conductivity SO4, and DOC in precipitation, soil water, and runoff chemistry from an upland peat-covered catchment in northern England. By deriving impulse transfer functions this study explores whether changes in deposition lead to significant changes in the occurrence of each component in the soil and runoff water; especially significant changes in DOC. The study shows that (1) impulses in the deposition of acidity have no significant effect upon pH or DOC in soil water or runoff. (2) DOC in soil water and runoff is responsive to impulses in SO4 and conductivity, but only when those impulses are changes in soil water chemistry and not when they are in atmospheric deposition. (3) The effects of changes in SO4 and/or conductivity can easily be overemphasized if memory effects are not accounted for, and their effect is limited to only 1 or 2 months after a severe drought. This study can support the view that changes in ionic strength can result in changes in DOC concentration in soil water or runoff, but the system studied is unresponsive to changes in atmospheric deposition. Impulses in soil water SO4 do not lead to increases in DOC concentrations, and so this mechanism does not provide an explanation for DOC increases.

Technical note: Evaluation of the diagnostic accuracy of 2 point-of-care β-hydroxybutyrate devices in stored bovine plasma at room temperature and at 37°C.

PubMed

Leal Yepes, F A; Nydam, D V; Heuwieser, W; Mann, S

2018-04-25

The use of point-of-care (POC) devices to measure blood metabolites, such as β-hydroxybutyrate (BHB), on farm have become an important diagnostic and screening tool in the modern dairy industry. The POC devices allow for immediate decision making and are often more economical than the use of laboratory-based methods; however, precision and accuracy may be lower when measurements are performed in an uncontrolled environment. Ideally, the advantages of the POC devices and the standardized laboratory environment could be combined when measuring samples that do not require an immediate result-for example, in research applications or when immediate intervention is not the goal. The objective of this study was to compare the capability of 2 POC devices (TaiDoc, Pharmadoc, Lübeck, Germany; Precision Xtra, Abbott Diabetes Care, Abingdon, UK) to measure BHB concentrations either at room temperature (RT; 20-22°C) or at 37°C compared with the gold standard test in stored plasma samples. Whole blood from multiparous Holstein dairy cows (n = 113) was sampled from the coccygeal vessels between 28 d before expected calving and 42 DIM. Whole-blood BHB concentrations were determined cow-side using the TaiDoc POC device. Plasma was separated within 1 h of collection and stored until analysis. A subset of stored plasma samples (n = 100) consisting of 1 sample per animal was chosen retrospectively based on the BHB concentrations in whole blood within the range of 0.2 to 4.0 mmol/L. The samples were analyzed for BHB plasma concentration using an automated chemistry analyzer (Hitachi 917, Hitachi, Tokyo, Japan), which was considered the gold standard. On the same day, the samples were also measured with the 2 POC devices, with samples either at RT or heated up to 37°C. Our study showed high Spearman correlation coefficients (>0.99) using either device and with samples at both temperatures compared with the gold standard. Passing-Bablok regression revealed a very strong correlation (>0.99), indicating good agreement between both POC devices and the gold standard method. For hyperketonemia detection, defined as BHB concentration ≥1.2 mmol/L, the sensitivity for both POC devices at RT and 37°C was equally high at 100%. Specificity was lowest (67.4%) for the TaiDoc used with plasma at RT and was highest (86.5%) when plasma was measured at 37°C with the Precision Xtra meter. Bland-Altman plots revealed a mean bias of 0.25 and 0.4 mmol/L for the Precision Xtra meter and TaiDoc, respectively, when tested on plasma at 37°C. Our data showed that both POC devices are suitable for measuring BHB concentration in stored bovine plasma, and accuracy was highest when samples were heated to 37°C compared with RT. Copyright © 2018 American Dairy Science Association. Published by Elsevier Inc. All rights reserved.

A study of dissolved organic carbon and nitrate export in Catskill Mountain watersheds

NASA Astrophysics Data System (ADS)

Son, K.; Moore, K. E.; Lin, L.; Schneiderman, E. M.; Band, L. E.

2016-12-01

Watersheds in the Catskill Mountain region of New York State have historically experienced soil and stream acidification due to deposition of acidic compounds created from atmospheric SO2 and NOx. Recent studies in this region, and elsewhere in North America and Europe, have shown increases in dissolved organic carbon (DOC) in streams and lakes. Watersheds in the Catskills are the major source of drinking water for New York City and other communities in the region. Due to use of chlorine for disinfection, there is potential for the increase in DOC to lead to increased levels of disinfection byproducts in treated drinking water. Therefore, developing an improved understanding of the sources, fate and transport mechanisms, and export patterns for nitrate and DOC is important for informing watershed and water supply management. In this study, we analyzed the relationships between watershed characteristics, nitrate, and DOC for 12 gauged streams in the Neversink River watershed. Watershed characteristics included topography (elevation, slope, topographic wetness index), vegetation (leaf area index, species composition), soil (soil hydraulic parameters, soil carbon, wetland soil), atmospheric deposition (SO2, NOx), and climate (precipitation, temperature). Our preliminary analysis showed that both watershed slope and baseflow ratio are negatively correlated with annual median DOC concentration. At Biscuit Brook in the Neversink watershed, annual precipitation explained about 25% of annual DOC median concentration. DOC concentration was highly correlated with storm runoff in spring, summer, and fall, but stream nitrate concentration was weakly correlated with storm runoff in most seasons except summer when it was highly correlated with baseflow. We also applied a process-based ecohydrologic model (Regional Hydrologic Ecologic System Simulation, RHESSys) to the Biscuit Brook watershed to explore sources of nitrate and DOC and their movement within the watershed. We expect that this study will increase our understanding of how, when, and where DOC and nitrate are stored and transported to streams, as well as give insights into the key controls on nitrate and DOC processes in Catskill Mountain watersheds.

Increases in dissolved organic carbon accelerate loss of toxic Al in Adirondack lakes recovering from acidification

USGS Publications Warehouse

Lawrence, Gregory B.; Dukett, James E; Houck, Nathan; Snyder, Phillip; Capone, Susan B.

2013-01-01

Increasing pH and decreasing Al in surface waters recovering from acidification have been accompanied by increasing concentrations of dissolved organic carbon (DOC) and associated organic acids that partially offset pH increases and complicate assessments of recovery from acidification. To better understand the processes of recovery, monthly chemistry from 42 lakes in the Adirondack region, NY, collected from 1994 to 2011, were used to (1) evaluate long-term changes in DOC and associated strongly acidic organic acids and (2) use the base-cation surplus (BCS) as a chemical index to assess the effects of increasing DOC concentrations on the Al chemistry of these lakes. Over the study period, the BCS increased (p < 0.01) and concentrations of toxic inorganic monomeric Al (IMAl) decreased (p < 0.01). The decreases in IMAl were greater than expected from the increases in the BCS. Higher DOC concentrations that increased organic complexation of Al resulted in a decrease in the IMAl fraction of total monomeric Al from 57% in 1994 to 23% in 2011. Increasing DOC concentrations have accelerated recovery in terms of decreasing toxic Al beyond that directly accomplished by reducing atmospheric deposition of strong mineral acids.

Increases in dissolved organic carbon accelerate loss of toxic Al in Adirondack lakes recovering from acidification.

PubMed

Lawrence, Gregory B; Dukett, James E; Houck, Nathan; Snyder, Phil; Capone, Sue

2013-07-02

Increasing pH and decreasing Al in surface waters recovering from acidification have been accompanied by increasing concentrations of dissolved organic carbon (DOC) and associated organic acids that partially offset pH increases and complicate assessments of recovery from acidification. To better understand the processes of recovery, monthly chemistry from 42 lakes in the Adirondack region, NY, collected from 1994 to 2011, were used to (1) evaluate long-term changes in DOC and associated strongly acidic organic acids and (2) use the base-cation surplus (BCS) as a chemical index to assess the effects of increasing DOC concentrations on the Al chemistry of these lakes. Over the study period, the BCS increased (p < 0.01) and concentrations of toxic inorganic monomeric Al (IMAl) decreased (p < 0.01). The decreases in IMAl were greater than expected from the increases in the BCS. Higher DOC concentrations that increased organic complexation of Al resulted in a decrease in the IMAl fraction of total monomeric Al from 57% in 1994 to 23% in 2011. Increasing DOC concentrations have accelerated recovery in terms of decreasing toxic Al beyond that directly accomplished by reducing atmospheric deposition of strong mineral acids.

Distribution and photoreactivity of chromophoric dissolved organic matter in northern Gulf of Mexico shelf waters

NASA Astrophysics Data System (ADS)

Shank, G. Christopher; Evans, Anne

2011-07-01

The distribution and photoreactivity of chromophoric dissolved organic matter (CDOM) in the northern Gulf of Mexico along the Louisiana coastal shelf were examined during three cruises in summer 2007, fall 2007, and summer 2008. The influence of the Mississippi River plume was clearly evident as CDOM levels (defined as a305) and dissolved organic carbon (DOC) concentrations were well-correlated with salinity during all cruises. Elevated CDOM and CDOM:DOC ratios of surface samples collected offshore of Atchafalaya Bay and the Breton-Chandeleur Sound complex indicated emanations of organic-rich waters from coastal wetlands are also an important source to nearshore shelf waters. Generally, CDOM and DOC levels were highest in surface waters and decreased with depth, but during summer 2007 and summer 2008, CDOM levels in near-bottom samples were occasionally higher than at mid-depths without concomitant increases in DOC. CDOM photobleaching was measured during 24 irradiations using a SunTest XLS+ solar simulator with photobleaching rate coefficients ( k305) ranging from 0.011 to 0.32 h -1. For fall 2007 and summer 2008, higher k305 values were generally observed in samples with higher initial CDOM levels. However, samples collected during summer 2007 did not exhibit a similar pattern nor were there differences in photobleaching rates between surface and bottom samples. Spectral slope coefficients ( S275-295 or S350-400) and DOC levels were largely unchanged after 24 h irradiations. Modeled CDOM photobleaching for northern Gulf of Mexico mid-shelf waters predicts that during the summer when solar irradiance is high and the water column becomes stratified, nearly 90% of the CDOM in the upper 1 m may be lost to photobleaching, with losses up to 20% possible even at 10 m depth.

The topographic wetness index as a predictor for hot spots of DOC export from catchments

NASA Astrophysics Data System (ADS)

Musolff, Andreas; Oosterwoud, Marieke; Tittel, Jörg; Selle, Benny; Fleckenstein, Jan H.

2015-04-01

Dissolved organic carbon (DOC) concentrations in the discharge of many catchments in Europe and North America are rising. This increase is of concern for the drinking water supply from reservoirs since high DOC concentrations cause additional costs in water treatment and potentially the formation of harmful disinfection by-products. A prerequisite for understanding this increase is the knowledge on the spatial distribution of dominant soil DOC sources within catchments and on mobilization as well as transfer processes to the surface water. A number of studies identified wetland soils as the dominant source with fast mobilization and short transit times to the receiving surface water. However, most studies have either focussed on smaller, hillslope and single catchment or on larger scale multi-catchment assessments. Moreover, information on the distribution of soil types in catchments is not always readily available. This study brings together both types of assessment in a data-driven top-down approach: (i) a detailed survey on DOC concentration and loads over the course of one year within two paired data-rich catchments discharging into a large drinking water reservoir in central Germany and (ii) a database of hydrochemistry and physio-geographic characteristics of 113 catchments draining into 58 reservoirs across Germany over the course of 16 years. The objective is to define hot spots of DOC export within the catchments for both types of assessments (i, ii) and to test the suitability of the topographic wetness index (TWI) as a proxy for well-connected wetland soils at various spatial scales. In the sub-catchments of assessment (i) the spatial variability of concentrations and loads was much smaller than expected. None of the studied sub-catchments was a predominant producer of the total DOC loads exported from the catchments. We found the mean concentrations and loads to be positively correlated with the share of groundwater-dominated soils in the sub-catchments. These soils are distributed in riparian wetlands along all streams within the catchments. As a readily available proxy for wetland soils percentiles of the probability distribution of the TWI in the sub-catchments were found to be good predictors for mean DOC concentrations in catchment outlet as well as for loads. In the larger dataset across Germany (ii) we also found a surprisingly good correlation between the TWI within the catchments and mean DOC concentrations. Thus we can show that, despite the wide range of topographies, land use types, geological setups and climatic conditions within this dataset the dominant source zones of DOC export is well captured by the TWI as a proxy for the share of wetland soils and DOC source zones within the catchments.

Influence of infrastructure on water quality and greenhouse gas dynamics in urban streams

NASA Astrophysics Data System (ADS)

Smith, Rose M.; Kaushal, Sujay S.; Beaulieu, Jake J.; Pennino, Michael J.; Welty, Claire

2017-06-01

Streams and rivers are significant sources of nitrous oxide (N2O), carbon dioxide (CO2), and methane (CH4) globally, and watershed management can alter greenhouse gas (GHG) emissions from streams. We hypothesized that urban infrastructure significantly alters downstream water quality and contributes to variability in GHG saturation and emissions. We measured gas saturation and estimated emission rates in headwaters of two urban stream networks (Red Run and Dead Run) of the Baltimore Ecosystem Study Long-Term Ecological Research project. We identified four combinations of stormwater and sanitary infrastructure present in these watersheds, including: (1) stream burial, (2) inline stormwater wetlands, (3) riparian/floodplain preservation, and (4) septic systems. We selected two first-order catchments in each of these categories and measured GHG concentrations, emissions, and dissolved inorganic and organic carbon (DIC and DOC) and nutrient concentrations biweekly for 1 year. From a water quality perspective, the DOC : NO3- ratio of streamwater was significantly different across infrastructure categories. Multiple linear regressions including DOC : NO3- and other variables (dissolved oxygen, DO; total dissolved nitrogen, TDN; and temperature) explained much of the statistical variation in nitrous oxide (N2O, r2 = 0.78), carbon dioxide (CO2, r2 = 0.78), and methane (CH4, r2 = 0.50) saturation in stream water. We measured N2O saturation ratios, which were among the highest reported in the literature for streams, ranging from 1.1 to 47 across all sites and dates. N2O saturation ratios were highest in streams draining watersheds with septic systems and strongly correlated with TDN. The CO2 saturation ratio was highly correlated with the N2O saturation ratio across all sites and dates, and the CO2 saturation ratio ranged from 1.1 to 73. CH4 was always supersaturated, with saturation ratios ranging from 3.0 to 2157. Longitudinal surveys extending form headwaters to third-order outlets of Red Run and Dead Run took place in spring and fall. Linear regressions of these data yielded significant negative relationships between each gas with increasing watershed size as well as consistent relationships between solutes (TDN or DOC, and DOC : TDN ratio) and gas saturation. Despite a decline in gas saturation between the headwaters and stream outlet, streams remained saturated with GHGs throughout the drainage network, suggesting that urban streams are continuous sources of CO2, CH4, and N2O. Our results suggest that infrastructure decisions can have significant effects on downstream water quality and greenhouse gases, and watershed management strategies may need to consider coupled impacts on urban water and air quality.

Temporal-spatial variation of DOC concentration, UV absorbance and the flux estimation in the Lower Dagu River, China

NASA Astrophysics Data System (ADS)

Xi, Min; Kong, Fanlong; Li, Yue; Kong, Fanting

2017-12-01

Dissolved organic carbon (DOC) is an important component for both carbon cycle and energy balance. The concentration, UV absorbance, and export flux of DOC in the natural environment dominate many important transport processes. To better understand the temporal and spatial variation of DOC, 7 sites along the Lower Dagu River were chosen to conduct a comprehensive measurement from March 2013 to February 2014. Specifically, water samples were collected from the Lower Dagu River between the 26th and 29th of every month during the experimental period. The DOC concentration (CDOC) and UV absorbance were analyzed using a total organic carbon analyzer and the ultraviolet-visible absorption spectrum, and the DOC export flux was estimated with a simple empirical model. The results showed that the CDOC of the Lower Dagu River varied from 1.32 to 12.56 mg/L, consistent with global rivers. The CDOC and UV absorbance showed significant spatial variation in the Dagu River during the experiential period because of the upstream natural processes and human activities in the watershed. The spatial variation is mainly due to dam or reservoir constructions, riverside ecological environment changes, and non-point source or wastewater discharge. The seasonal variation of CDOC was mainly related to the source of water DOC, river runoff, and temperature, and the UV absorbance and humification degree of DOC had no obvious differences among months ( P<0.05). UV absorbance was applied to test the CDOC in Lower Dagu River using wave lengths of 254 and 280 nm. The results revealed that the annual DOC export flux varied from 1.6 to 3.76 × 105 g C/km2/yr in a complete hydrological year, significantly lower than the global average. It is worth mentioning that the DOC export flux was mainly concentrated in summer (˜90% of all-year flux in July and August), since the runoff in the Dagu River took place frequently in summer. These observations implied environment change could bring the temporal-spatial variation of DOC and the exports, which would further affect the land-ocean interactions in the Lower Dagu River and the global carbon cycle.

Fluvial dissolved organic carbon composition varies spatially and seasonally in a small catchment draining a wind farm and felled forestry.

PubMed

Zheng, Ying; Waldron, Susan; Flowers, Hugh

2018-06-01

Assessing whether land use, from activities such as wind farm construction and tree-felling, impacts on terrestrial C delivery to rivers has focused on quantifying the loss of dissolved organic carbon (DOC), and not the composition changes. Here we explore how land use influences DOC composition by considering fluvial DOC concentration, [DOC], and spectrophotometric composition of a river draining a peat-rich catchment. We find that in this 5.7km 2 catchment differences occur in both the concentration and composition of the DOC in its sub-catchments. This is attributed to differences in how land was used: one tributary (D-WF) drains an area with wind farm construction and forestry in the headwaters, and one tributary (D-FF) drains an area with felled plantation trees. Generally, [DOC] in both streams showed similar seasonal variation, and autumn maxima. However, the felled catchment had greater mean [DOC] than the wind farm catchment. The SUVA 254 and E 4 /E 6 indicated DOC in both streams had similar aromaticity and fulvic:humic acid for most of the time, but SUVA 410 and E 2 /E 4 indicated less DOC humification in the felled catchment. This may be due to young DOC from the breakdown of residual branches and roots, or more humification in soils in the wind farm area. During the dry months, DOC composition showed more spatial variation: the D-WF DOC had smaller SUVA 254 (less total aromatic material) and SUVA 410 (fewer humic substances). The decreased E 2 /E 4 in both streams indicated the total aromatic carbon decreased more than humic substances content. Moreover, the larger E 4 /E 6 for D-WF in summer indicated that the humic substances were richer in fulvic acids than humic acids. Soil disturbance associated with forestry-felling likely contributed to the higher [DOC] and release of less-humified material in D-FF. This research indicates drivers of different DOC concentration and composition can exist even in small catchments. Copyright © 2018 Elsevier B.V. All rights reserved.

Regulation of stream water dissolved organic carbon concentrations ([DOC]) during snowmelt in forest streams; the role of discharge, winter climate and memory effects

NASA Astrophysics Data System (ADS)

Ågren, A.; Haei, M.; Öquist, M.; Buffam, I.; Ottosson-Löfvenius, M.; Kohler, S.; Bishop, K.; Blomkvist, P.; Laudon, H.

2011-12-01

Using 15 year stream records from two forested northern boreal catchments, coupled with soil frost experiments in the riparian zone, we demonstrate the complex inter-annual control on [DOC] and export during snowmelt. Stream [DOC] varied by a factor of 2 during those 15 years with no consistent trend. Based on our long-term analysis, we demonstrate, for the first time, that stream water [DOC] is strongly linked to the climatic conditions during the preceding winter, but that there is also a long-term memory effect in the catchment soils, related to the extent of the previous export from the catchment. Hydrology had a first order control on the inter-annual variation in concentrations, and the length of the winter was more important than the memory effect. By removing the effect of discharge on [DOC], using a conceptual hydrological model, we could detect processes that would otherwise have been overshadowed. A short and intense snowmelt gave higher [DOC] in the stream. During a prolonged snowmelt, one soil layer at the time might have been "flushed" from easily exported DOC, resulting in slightly lower stream [DOC] during such years. We found that longer and colder winters resulted in higher [DOC] during the subsequent snowmelt. A soil frost manipulation experiment in the riparian soils of the study catchment showed that the DOC concentrations in the soil water increased with the duration of the soil frost. A high antecedent DOC export during the preceding summer and autumn resulted in lower concentrations during the following spring, indicating a long-term "memory effect" of the catchment soils. In a nearby stream draining mire, we found a different response to hydrology but similar response to climate and memory effect. The inter-annual variation in snowmelt DOC exports was mostly controlled by the amount of runoff, but the variability in [DOC] also exerted a significant control on the exports, accounting for 15% of the variance in exports. We conclude that winter climatic conditions can play a substantial role in controlling stream [DOC] in ways not previously understood. These findings are especially important for northern latitude regions expected to be most affected by climate change. It's difficult to directly translate this to a future climate change prediction. If warmer winters with less insulating snow cover increase the soil frost, the results from the soil frost manipulation experiment then suggest increasing [DOC] in a future climate. At the same time the statistical analysis of the stream records suggest that a shorter and warmer winter would decrease the [DOC]. Our results do, however, highlight the role of winter climate for regulating DOC in areas with seasonally frozen soils which should be considered when resolving the sensitivity of stream [DOC] to global environmental change.

A Global Assessment of Rain-Dissolved Organic Carbon

NASA Astrophysics Data System (ADS)

Safieddine, S.; Heald, C. L.

2017-12-01

Precipitation is the largest physical removal pathway of atmospheric organic carbon from the atmosphere. The removed carbon is transferred to the land and ocean in the form of dissolved organic carbon (DOC). Limited measurements have hindered efforts to characterize global DOC. In this poster presentation, we show the first simulated global DOC distribution based on a GEOS-Chem model simulation of the atmospheric reactive carbon budget. Over the ocean, simulated DOC concentrations are between 0.1 to 1 mgCL-1 with a total of 85 TgCyr-1 deposited. DOC concentrations are higher inland, ranging between 1 and 10 mgCL-1, producing a total of 188 TgCyr-1 terrestrial organic wet deposition. We compare the 2010 simulated DOC to a 30-year synthesis of available DOC measurements over different environments. Despite imperfect matching of observational and simulated time intervals, the model is able to reproduce much of the spatial variability of DOC (r= 0.63), with a low bias of 35%. We compare the global average carbon oxidation state (OSc) of both atmospheric and dissolved organic carbon, as a simple metric for describing the chemical composition of organics. In the global atmosphere reactive organic carbon (ROC) is dominated by hydrocarbons and ketones, and OSc, ranges from -1.8 to -0.6. In the dissolved form, formaldehyde, formic acid, primary and secondary semi-volatiles organic aerosol dominate the DOC concentrations. The increase in solubility upon oxidation leads to a global increase in OSc in rainwater with -0.6<=OSc <=0. This simulation provides new insight into the current model representation of the flow of atmospheric and rain-dissolved organic carbon, and new opportunities to use observations and simulations to understand the DOC reaching land and ocean.

Persistent Influences of the 2002 Hayman Fire on Stream Nitrate and Dissolved Organic Carbon

NASA Astrophysics Data System (ADS)

Rhoades, C.; Pierson, D. N.; Fegel, T. S., II; Chow, A. T.; Covino, T. P.

2016-12-01

Large, high severity wildfires alter the physical and biological conditions that determine how watersheds retain and release nutrients and regulate stream water quality. For five years after the 2002 Hayman Fire burned in Colorado conifer forests, stream nitrate concentrations and export increased steadily in watersheds with extensive high-severity burning. Stream temperature and turbidity also increased in relation to the extent of high-severity burning and remained elevated above background levels throughout the initial five year post-fire period. Our recent sampling documents that 14 years after the Hayman Fire stream nitrate remains an order of magnitude higher in extensively-burned (35-90%) compared to unburned watersheds (0.2 vs 2.8 mg L-1). Nitrate represents 83% of the total dissolved N in extensively-burned watersheds compared to 29% in unburned watersheds. In contrast, dissolved organic carbon (DOC), was highest in watersheds that burned to a moderate extent (10-20%) and lowest in those with extensive burning. Catchments with a moderate extent burned had DOC concentrations 2.5 and 1.7 times more than those with extensive burning and unburned catchments, respectively. Peak concentrations of DOC and nitrate track the rising limb of the streamflow hydrograph and reach a maximum in May, but patterns among burn extent categories were seasonally consistent. Current riparian conditions are linked to stream nitrate in burned watersheds. For example, stream nitrate increases proportionally to the extent of riparian zones with low shrub cover (R2 = 0.76). We found signs of watershed recovery compared to the initial post-fire period; stream temperature and turbidity remained elevated in extensively burned catchments, but increases were only significant during the spring season. The persistent stream nitrate concentrations as well as the relation between riparian cover and post-fire stream nitrate may help prioritize restoration planting efforts and mitigate chronic, elevated nitrate export from burned watersheds.

Permafrost thaw and climate warming may decrease the CO2, carbon, and metal concentration in peat soil waters of the Western Siberia Lowland.

PubMed

Raudina, T V; Loiko, S V; Lim, A; Manasypov, R M; Shirokova, L S; Istigechev, G I; Kuzmina, D M; Kulizhsky, S P; Vorobyev, S N; Pokrovsky, O S

2018-09-01

Soil pore waters are a vital component of the ecosystem as they are efficient tracers of mineral weathering, plant litter leaching, and nutrient uptake by vegetation. In the permafrost environment, maximal hydraulic connectivity and element transport from soils to rivers and lakes occurs via supra-permafrost flow (i.e. water, gases, suspended matter, and solutes migration over the permafrost table). To assess possible consequences of permafrost thaw and climate warming on carbon and Green House gases (GHG) dynamics we used a "substituting space for time" approach in the largest frozen peatland of the world. We sampled stagnant supra-permafrost (active layer) waters in peat columns of western Siberia Lowland (WSL) across substantial gradients of climate (-4.0 to -9.1°C mean annual temperature, 360 to 600mm annual precipitation), active layer thickness (ALT) (>300 to 40cm), and permafrost coverage (sporadic, discontinuous and continuous). We analyzed CO 2 , CH 4 , dissolved carbon, and major and trace elements (TE) in 93 soil pit samples corresponding to several typical micro landscapes constituting the WSL territory (peat mounds, hollows, and permafrost subsidences and depressions). We expected a decrease in intensity of DOC and TE mobilization from soil and vegetation litter to the supra-permafrost water with increasing permafrost coverage, decreasing annual temperature and ALT along a latitudinal transect from 62.3°N to 67.4°N. However, a number of solutes (DOC, CO 2 , alkaline earth metals, Si, trivalent and tetravalent hydrolysates, and micronutrients (Mn, Co, Ni, Cu, V, Mo) exhibited a northward increasing trend with highest concentrations within the continuous permafrost zone. Within the "substituting space for time" climate change scenario and northward shift of the permafrost boundary, our results suggest that CO 2 , DOC, and many major and trace elements will decrease their concentration in soil supra-permafrost waters at the boundary between thaw and frozen layers. As a result, export of DOC and elements from peat soil to lakes and rivers of the WSL (and further to the Arctic Ocean) may decrease. Copyright © 2018 Elsevier B.V. All rights reserved.

Source water controls on the character and origin of dissolved organic matter in streams of the Yukon River basin, Alaska

USGS Publications Warehouse

O'Donnell, Jonathan A.; Aiken, George R.; Kane, Evan S.; Jones, Jeremy B.

2010-01-01

Climate warming and permafrost degradation at high latitudes will likely impact watershed hydrology, and consequently, alter the concentration and character of dissolved organic carbon (DOC) in northern rivers. We examined seasonal variation of DOC chemistry in 16 streams of the Yukon River basin, Alaska. Our primary objective was to evaluate the relationship between source water (shallow versus deep groundwater flow paths) and DOC chemical composition. Using base cation chemistry and principal component analysis, we observed high contributions of deep groundwater to glacial and clearwater streams, whereas blackwater streams received larger contributions from shallow groundwater sources. DOC concentration and specific ultraviolet absorbance peaked during spring snowmelt in all streams, and were consistently higher in blackwater streams than in glacial and clearwater streams. The hydrophobic acid fraction of DOC dominated across all streams and seasons, comprising between 35% and 56% of total DOC. The hydrophilic acid fraction of DOC was more prominent in glacial (23% ± 3%) and clearwater streams (19% ± 1%) than in blackwater streams (16% ± 1%), and was enriched during winter base flow (29% ± 1%) relative to snowmelt and summer base flow. We observed that an increase in the contribution of deep groundwater to streamflow resulted in decreased DOC concentration, aromaticity, and DOC-to-dissolved organic nitrogen ratio, and an increase in the proportion of hydrophilic acids relative to hydrophobic acids. Our findings suggest that future permafrost degradation and higher contributions of groundwater to streamflow may result in a higher fraction of labile DOM in streams of the Yukon basin.

Influences of observation method, season, soil depth, land use and management practice on soil dissolvable organic carbon concentrations: A meta-analysis.

PubMed

Li, Siqi; Zheng, Xunhua; Liu, Chunyan; Yao, Zhisheng; Zhang, Wei; Han, Shenghui

2018-08-01

Quantifications of soil dissolvable organic carbon concentrations, together with other relevant variables, are needed to understand the carbon biogeochemistry of terrestrial ecosystems. Soil dissolvable organic carbon can generally be grouped into two incomparable categories. One is soil extractable organic carbon (EOC), which is measured by extracting with an aqueous extractant (distilled water or a salt solution). The other is soil dissolved organic carbon (DOC), which is measured by sampling soil water using tension-free lysimeters or tension samplers. The influences of observation methods, natural factors and management practices on the measured concentrations, which ranged from 2.5-3970 (mean: 69) mg kg -1 of EOC and 0.4-200 (mean: 12) mg L -1 of DOC, were investigated through a meta-analysis. The observation methods (e.g., extractant, extractant-to-soil ratio and pre-treatment) had significant effects on EOC concentrations. The most significant divergence (approximately 109%) occurred especially at the extractant of potassium sulfate (K 2 SO 4 ) solutions compared to distilled water. As EOC concentrations were significantly different (approximately 47%) between non-cultivated and cultivated soils, they were more suitable than DOC concentrations for assessing the influence of land use on soil dissolvable organic carbon levels. While season did not significantly affect EOC concentrations, DOC concentrations showed significant differences (approximately 50%) in summer and autumn compared to spring. For management practices, applications of crop residues and nitrogen fertilizers showed positive effects (approximately 23% to 91%) on soil EOC concentrations, while tillage displayed negative effects (approximately -17%), compared to no straw, no nitrogen fertilizer and no tillage. Compared to no nitrogen, applications of synthetic nitrogen also appeared to significantly enhance DOC concentrations (approximately 32%). However, further studies are needed in the future to confirm/investigate the effects of ecosystem management practices using standardized EOC measurement protocols or more DOC cases of field experiments. Copyright © 2018 Elsevier B.V. All rights reserved.

Mapping Surface Water DOC in the Northern Gulf of Mexico Using CDOM Absorption Coefficients and Remote Sensing Imagery

NASA Astrophysics Data System (ADS)

Kelly, B.; Chelsky, A.; Bulygina, E.; Roberts, B. J.

2017-12-01

Remote sensing techniques have become valuable tools to researchers, providing the capability to measure and visualize important parameters without the need for time or resource intensive sampling trips. Relationships between dissolved organic carbon (DOC), colored dissolved organic matter (CDOM) and spectral data have been used to remotely sense DOC concentrations in riverine systems, however, this approach has not been applied to the northern Gulf of Mexico (GoM) and needs to be tested to determine how accurate these relationships are in riverine-dominated shelf systems. In April, July, and October 2017 we sampled surface water from 80+ sites over an area of 100,000 km2 along the Louisiana-Texas shelf in the northern GoM. DOC concentrations were measured on filtered water samples using a Shimadzu TOC-VCSH analyzer using standard techniques. Additionally, DOC concentrations were estimated from CDOM absorption coefficients of filtered water samples on a UV-Vis spectrophotometer using a modification of the methods of Fichot and Benner (2011). These values were regressed against Landsat visible band spectral data for those same locations to establish a relationship between the spectral data, CDOM absorption coefficients. This allowed us to spatially map CDOM absorption coefficients in the Gulf of Mexico using the Landsat spectral data in GIS. We then used a multiple linear regressions model to derive DOC concentrations from the CDOM absorption coefficients and applied those to our map. This study provides an evaluation of the viability of scaling up CDOM absorption coefficient and remote-sensing derived estimates of DOC concentrations to the scale of the LA-TX shelf ecosystem.

Dynamics, chemical properties and bioavailability of DOC in an early successional catchment

NASA Astrophysics Data System (ADS)

Risse-Buhl, U.; Hagedorn, F.; Dümig, A.; Gessner, M. O.; Schaaf, W.; Nii-Annang, S.; Gerull, L.; Mutz, M.

2013-01-01

The dynamics of dissolved organic carbon (DOC) have been intensively studied in mature ecosystems, but little is known about DOC dynamics and the significance of DOC as a substrate for microbial activity in early-successional catchments. We determined the concentration, chemical composition, source, radiocarbon age, and bioavailability of DOC along the hydrological flow path from soil solution to a downstream pond in a recently constructed catchment (Chicken Creek Catchment, Germany). Soil solution, upwelling ground water, subsurface water in an alluvial fan, and pond water all had high DOC concentrations (averages of 6.0-11.6 mg DOC L-1), despite small carbon stocks in either vegetation or soil of the early-successional catchment. The mean 14C age of DOC in upwelling ground water was 2600 to 2800 yr. Solid-state CPMAS 13C NMR revealed a higher proportion of aromatic compounds (32%) and a lower proportion of carbohydrates (33%) in upwelling ground water than in pond water (18% and 45%, respectively). The 14C age and 13C NMR spectra suggest that DOC was partly mobilized from charred organic matter of the Quaternary substrate. In an experimental 70-days incubation experiment, 20% of the total DOC was found to be bioavailable, irrespective of the water type. Origin of microbial communities (enriched from soil, stream sediment or pond water) had only marginal effects on overall DOC utilization. Overall, these data suggest that the old DOC can support microbial activity during early ecosystem succession to some extent, although the largest fraction is recalcitrant DOC that is exported from the catchment once it has been mobilized.

Soil Fauna Affects Dissolved Carbon and Nitrogen in Foliar Litter in Alpine Forest and Alpine Meadow

PubMed Central

Liao, Shu; Yang, Wanqin; Tan, Yu; Peng, Yan; Li, Jun; Tan, Bo; Wu, Fuzhong

2015-01-01

Dissolved organic carbon (DOC) and total dissolved nitrogen (TDN) are generally considered important active biogeochemical pools of total carbon and nitrogen. Many studies have documented the contributions of soil fauna to litter decomposition, but the effects of the soil fauna on labile substances (i.e., DOC and TDN) in litter during early decomposition are not completely clear. Therefore, a field litterbag experiment was carried out from 13th November 2013 to 23rd October 2014 in an alpine forest and an alpine meadow located on the eastern Tibetan Plateau. Litterbags with different mesh sizes were used to provide access to or prohibit the access of the soil fauna, and the concentrations of DOC and TDN in the foliar litter were measured during the winter (the onset of freezing, deep freezing and thawing stage) and the growing season (early and late). After one year of field incubation, the concentration of DOC in the litter significantly decreased, whereas the TDN concentration in the litter increased. Similar dynamic patterns were detected under the effects of the soil fauna on both DOC and TDN in the litter between the alpine forest and the alpine meadow. The soil fauna showed greater positive effects on decreasing DOC concentration in the litter in the winter than in the growing season. In contrast, the dynamics of TND in the litter were related to seasonal changes in environmental factors, rather than the soil fauna. In addition, the soil fauna promoted a decrease in litter DOC/TDN ratio in both the alpine forest and the alpine meadow throughout the first year of decomposition, except for in the late growing season. These results suggest that the soil fauna can promote decreases in DOC and TDN concentrations in litter, contributing to early litter decomposition in these cold biomes. PMID:26406249

The role of dissolved organic carbon concentration and composition on nickel toxicity to early life-stages of the blue mussel Mytilus edulis and purple sea urchin Strongylocentrotus purpuratus.

PubMed

Blewett, Tamzin A; Dow, Elissa M; Wood, Chris M; McGeer, James C; Smith, D Scott

2018-05-24

Nickel (Ni) emissions resulting from production and transportation raise concerns about the impact of Ni exposure to marine ecosystems. Ni bioavailability models are established for FW systems, but the influence of chemical parameters (e.g. dissolved organic carbon (DOC)) on Ni toxicity within marine systems is less well understood. To examine the effects of DOC concentration and composition on Ni toxicity, acute toxicity tests were conducted on early life-stages of blue mussels (Mytilus edulis) and sea urchin embryos (Strongylocentrotus purpuratus) in full strength sea water (32 ppt). Nine different field collected samples of water with varying concentration (up to 4.5 mg C/L) and composition of DOC were collected from the east coast of the United States. Organic matter compositional analysis included molecular fluorescence and absorbance spectroscopy. The different DOC sources had different protective effects against embryo toxicity. The control (no DOC) Ni 48 h-EC 50 for Mytilus embryos was 133 µg/L (95% confidence interval (C.I.) of 123-144 µg/L), while Strongylocentrotus embryos displayed control 96-h EC 50 values of 207 µg/L (167-247 µg/L). The most significantly protective sample had high humic acid concentrations (as determined from fluorescence spectroscopy), which yielded an EC 50 of 195 µg/L (169-222 µg/L) for Mytilus, and an EC 50 of 394 µg/L (369-419 µg/L) for S. purpuratus. Among all samples, protection was related to both DOC quantity and quality, with fluorescence-resolved humic and fulvic acid concentrations showing the strongest correlations with protection for both species. These data suggest that DOC is protective against Ni toxicity in M. edulis and S. purpuratus, and that accounting for a DOC quality factor will improve predictive toxicity models such as the biotic ligand model. Copyright © 2018 Elsevier Inc. All rights reserved.

Evaluation of acute copper toxicity to juvenile freshwater mussels (fatmucket, lampsilis siliquoidea) in natural and reconstituted waters

USGS Publications Warehouse

Wang, N.; Mebane, C.A.; Kunz, J.L.; Ingersoll, C.G.; May, T.W.; Arnold, W.R.; Santore, R.C.; Augspurger, T.; Dwyer, F.J.; Barniiart, M.C.

2009-01-01

The influence of dissolved organic carbon (DOC) and water composition on the toxicity of copper to juvenile freshwater mussels (fatmucket, Lampsilis siliquoidea) were evaluated in natural and reconstituted waters. Acute 96-h copper toxicity tests were conducted at four nominal DOC concentrations (0, 2.5, 5, and 10 mg/L as carbon [C]) in dilutions of natural waters and in American Society for Testing and Materials (ASTM) reconstituted hard water. Toxicity tests also were conducted in ASTM soft, moderately hard, hard, and very hard reconstituted waters (nominal hardness 45-300 mg/L as CaCO3). Three natural surface waters (9.5-11 mg/L DOC) were diluted to obtain a series of DOC concentrations with diluted well water, and an extract of natural organic matter and commercial humic acid was mixed with ASTM hard water to prepare a series of DOC concentrations for toxicity testing. Median effective concentrations (EC50s) for dissolved copper varied >40-fold (9.9 to >396 ??g Cu/L) over all 21 treatments in various DOC waters. Within a particular type of DOC water, EC50s increased 5- to 12-fold across DOC concentrations of 0.3 to up to 11 mg C/L. However, EC50s increased by only a factor of 1.4 (21 30 ??g Cu/L) in the four ASTM waters with wide range of water hardness (52-300 mg CaCO 3/L). Predictions from the biotic ligand model (BLM) for copper explained nearly 90% of the variability in EC50s. Nearly 70% of BLM-normalized EC50s for fatmucket tested in natural waters were below the final acute value used to derive the U.S. Environmental Protection Agency acute water quality criterion for copper, indicating that the criterion might not be protective of fatmucket and perhaps other mussel species. ?? 2009 SETAC.

Soil Fauna Affects Dissolved Carbon and Nitrogen in Foliar Litter in Alpine Forest and Alpine Meadow.

PubMed

Liao, Shu; Yang, Wanqin; Tan, Yu; Peng, Yan; Li, Jun; Tan, Bo; Wu, Fuzhong

2015-01-01

Dissolved organic carbon (DOC) and total dissolved nitrogen (TDN) are generally considered important active biogeochemical pools of total carbon and nitrogen. Many studies have documented the contributions of soil fauna to litter decomposition, but the effects of the soil fauna on labile substances (i.e., DOC and TDN) in litter during early decomposition are not completely clear. Therefore, a field litterbag experiment was carried out from 13th November 2013 to 23rd October 2014 in an alpine forest and an alpine meadow located on the eastern Tibetan Plateau. Litterbags with different mesh sizes were used to provide access to or prohibit the access of the soil fauna, and the concentrations of DOC and TDN in the foliar litter were measured during the winter (the onset of freezing, deep freezing and thawing stage) and the growing season (early and late). After one year of field incubation, the concentration of DOC in the litter significantly decreased, whereas the TDN concentration in the litter increased. Similar dynamic patterns were detected under the effects of the soil fauna on both DOC and TDN in the litter between the alpine forest and the alpine meadow. The soil fauna showed greater positive effects on decreasing DOC concentration in the litter in the winter than in the growing season. In contrast, the dynamics of TND in the litter were related to seasonal changes in environmental factors, rather than the soil fauna. In addition, the soil fauna promoted a decrease in litter DOC/TDN ratio in both the alpine forest and the alpine meadow throughout the first year of decomposition, except for in the late growing season. These results suggest that the soil fauna can promote decreases in DOC and TDN concentrations in litter, contributing to early litter decomposition in these cold biomes.

Formation of trihalomethanes of dissolved organic matter fractions in reservoir and canal waters.

PubMed

Musikavong, Charongpun; Srimuang, Kanjanee; Tachapattaworakul Suksaroj, Thunwadee; Suksaroj, Chaisri

2016-07-28

The formation of trihalomethanes (THMs) of hydrophobic organic fraction (HPO), transphilic organic fraction (TPI), and hydrophilic organic fraction (HPI) of reservoir and canal waters from the U-Tapao River Basin, Songkhla, Thailand was investigated. Water samples were collected three times from two reservoirs, upstream, midstream, and downstream of the U-Tapao canal. The HPO was the major dissolved organic matter (DOM) fraction in reservoir and canal waters. On average, the HPO accounted for 53 and 45% of the DOM in reservoir and canal waters, respectively. The TPI of 19 and 23% in reservoir and canal waters were determined, respectively. The HPI of 29% of the reservoir water and HPI of 32% of the canal water were detected. For the reservoir water, the highest trihalomethane formation potential (THMFP)/dissolved organic carbon (DOC) was determined for the HPI, followed by the TPI and HPO, respectively. The average values of the THMFP/DOC of the HPI, TPI, and HPO of the reservoir water were 78, 52, and 49 µg THMs/mg C, respectively. The highest THMFP/DOC of the canal water was detected for the HPI, followed by HPO and TPI, respectively. Average values of the THMFP/DOC of HPI of water at upstream and midstream locations of 58 µg THMs/mg C and downstream location of 113 µg THMs/mg C were determined. Average values of THMFP/DOC of HPO of water at upstream and midstream and downstream locations were 48 and 93 µg THMs/mg C, respectively. For the lowest THMFP/DOC fraction, the average values of THMFP/DOC of TPI of water at upstream and midstream and downstream locations were 35 and 73 µg THMs/mg C, respectively.

Towards a better understanding aquatic carbon losses from lowland peatlands across England and Wales

NASA Astrophysics Data System (ADS)

Grayson, Richard; Holden, Joseph; Chapman, Pippa; Evans, Chris

2017-04-01

Hydrological fluxes in lowland peatlands can be challenging to measure but they drive poorly understood aquatic carbon fluxes which may form an important part of the overall carbon budget for peatlands. In this study we examined 11 lowland peatland sites across some of the most important fen and raised bog complexes in England and Wales including agricultural peatlands, mining sites and restoration sites. These were intensively monitored between January 2013 and December 2015. The monitoring included continual hydrological measurements and regular sampling for dissolved organic and inorganic carbon (DOC and DIC), particulate organic carbon (POC) and dissolved carbon dioxide, methane and nitrous oxide. These data were used to calculate the amount of water flowing out of each site and the total aquatic carbon loss. In addition, the hydrological data were used to provide contextual data to explain carbon flux variations between sites and help explain and model variations in gaseous carbon fluxes. The hydrology of all these lowland peat sites is typically complex with most having been drained, which when combined with their relatively flat gradients results in most having no clear single outlet. In addition the drainage networks are often used to not only drain water during periods of excess rainfall but also to maintain raised water tables during summer months when rainfall totals are low. As a result, aquatic losses were determined using a mixture of water mass balance approaches (e.g. using flux tower evapotranspiration data) and groundwater flow monitoring. The hydrology of the 11 sites was found to vary considerably, even between co-located sites, however as might be expected given the west-east rainfall gradient observed in the UK, discharge was typically highest at the Anglesey Fens sites (western Wales) and lowest at the East Anglian Fens sites (eastern England). One influence on the observed differences in discharge was the impact of vegetation type on evapotranspiration rates, with sites with high ET having some of the lowest discharge. Compared to gaseous fluxes, aquatic carbon fluxes made a smaller but significant contribution to overall rates of carbon loss, with the 'reactive' aquatic C flux accounting for 2-26% of NEE. Dissolved organic carbon (DOC) made the largest contribution. Concentrations of DOC were generally high, with all sites having mean concentrations greater than 20 mg L-1. DOC fluxes ranged from just 4 g C m-2 yr-1 up to 67 g C m-2 yr-1 being more variable than concentrations due to the wide variation in discharge from the different sites. Fluxes were highest from the raised bog sites and lowest from the fen sites.

Dynamics, chemical properties and bioavailability of DOC in an early successional catchment

NASA Astrophysics Data System (ADS)

Risse-Buhl, U.; Hagedorn, F.; Dümig, A.; Gessner, M. O.; Schaaf, W.; Nii-Annang, S.; Gerull, L.; Mutz, M.

2013-07-01

The dynamics of dissolved organic carbon (DOC) have been intensively studied in mature ecosystems, but little is known about DOC dynamics and the significance of DOC as a substrate for microbial activity in early-successional catchments. We determined the concentration, chemical composition, source, radiocarbon age, and bioavailability of DOC along the hydrological flow path from soil solution to a downstream pond in a recently constructed catchment (Chicken Creek Catchment, Germany). Soil solution, upwelling ground water, stream water, subsurface water in an alluvial fan, and pond water all had high DOC concentrations (averages: 6.0-11.6 mg DOC L-1), despite small carbon stocks in both vegetation and soil of the catchment. Solid-state CPMAS 13C NMR of DOC in upwelling ground water revealed a higher proportion of aromatic compounds (32%) and a lower proportion of carbohydrates (33%) than in pond water (18% and 45%, respectively). The average 14C age of DOC in upwelling ground water was 2600 to 2900 yr, while organic matter of the Quaternary substrate of the catchment had a 14C age of 3000 to 16 000 yr. Both the 14C age data and 13C NMR spectra suggest that DOC partly derived from organic matter of the Quaternary substrate (about 40 to 90% of the C in the DOC), indicating that both recent and old C of the DOC can support microbial activity during early ecosystem succession. However, in a 70 day incubation experiment, only about 11% of the total DOC was found to be bioavailable. This proportion was irrespective of the water type. Origin of the microbial communities within the catchment (enriched from soil, stream sediment or pond water) also had only a marginal effect on overall DOC utilization.

Dissolved Organic Matter Land-Ocean Linkages in the Arctic

NASA Astrophysics Data System (ADS)

Mann, P. J.; Spencer, R. M.; Hernes, P. J.; Tank, S. E.; Striegl, R.; Dyda, R. Y.; Peterson, B. J.; McClelland, J. W.; Holmes, R. M.

2012-04-01

Rivers draining into the Arctic Ocean exhibit high concentrations of terrigenous dissolved organic carbon (DOC), and recent studies indicate that DOC export is changing due to climatic warming and alteration in permafrost condition. The fate of exported DOC in the Arctic Ocean is important for understanding the regional carbon cycle and remains a point of discussion in the literature. As part of the NSF funded Arctic Great Rivers Observatory (Arctic-GRO) project, samples were collected for DOC, chromophoric and fluorescent dissolved organic matter (CDOM & FDOM) and lignin phenols from the Ob', Yenisey, Lena, Kolyma, Mackenzie and Yukon rivers in 2009 - 2010. DOC and lignin concentrations were elevated during the spring freshet and measurements related to DOC composition indicated an increasing contribution from terrestrial vascular plant sources at this time of year (e.g. lignin carbon-normalized yield, CDOM spectral slope, SUVA254, humic-like fluorescence). CDOM absorption was found to correlate strongly with both DOC (r2=0.83) and lignin concentration (r2=0.92) across the major arctic rivers. Lignin composition was also successfully modeled using FDOM measurements decomposed using PARAFAC analysis. Utilizing these relationships we modeled loads for DOC and lignin export from high-resolution CDOM measurements (daily across the freshet) to derive improved flux estimates, particularly from the dynamic spring discharge maxima period when the majority of DOC and lignin export occurs. The new load estimates for DOC and lignin are higher than previous evaluations, emphasizing that if these are more representative of current arctic riverine export, terrigenous DOC is transiting through the Arctic Ocean at a faster rate than previously thought. It is apparent that higher resolution sampling of arctic rivers is exceptionally valuable with respect to deriving accurate fluxes and we highlight the potential of CDOM in this role for future studies and the applicability of in-situ CDOM sensors.

Dissolved oxygen as an indicator of bioavailable dissolved organic carbon in groundwater

USGS Publications Warehouse

Chapelle, Francis H.; Bradley, Paul M.; McMahon, Peter B.; Kaiser, Karl; Benner, Ron

2012-01-01

Concentrations of dissolved oxygen (DO) plotted vs. dissolved organic carbon (DOC) in groundwater samples taken from a coastal plain aquifer of South Carolina (SC) showed a statistically significant hyperbolic relationship. In contrast, DO-DOC plots of groundwater samples taken from the eastern San Joaquin Valley of California (CA) showed a random scatter. It was hypothesized that differences in the bioavailability of naturally occurring DOC might contribute to these observations. This hypothesis was examined by comparing nine different biochemical indicators of DOC bioavailability in groundwater sampled from these two systems. Concentrations of DOC, total hydrolysable neutral sugars (THNS), total hydrolysable amino acids (THAA), mole% glycine of THAA, initial bacterial cell counts, bacterial growth rates, and carbon dioxide production/consumption were greater in SC samples relative to CA samples. In contrast, the mole% glucose of THNS and the aromaticity (SUVA254) of DOC was greater in CA samples. Each of these indicator parameters were observed to change with depth in the SC system in a manner consistent with active biodegradation. These results are uniformly consistent with the hypothesis that the bioavailability of DOC is greater in SC relative to CA groundwater samples. This, in turn, suggests that the presence/absence of a hyperbolic DO-DOC relationship may be a qualitative indicator of relative DOC bioavailability in groundwater systems.

Where does boreal stream DOC come from? - Quantifying the contribution from different landscape compartments using stable C isotope ratios.

NASA Astrophysics Data System (ADS)

Brink Bylund, J.; Bastviken, D.; Morth, C.; Laudon, H.; Giesler, R.; Buffam, I.

2007-12-01

Stable carbon isotope (δ13C) ratios are frequently used as a source tracer of e.g. organic matter (OM) produced in terrestrial versus aquatic environments. To our knowledge there has been no previous attempt to quantify the relative contribution of dissolved organic carbon (DOC) from various landscape compartments in catchments of different sizes. Here, we test to what extent δ13C values can be used also to quantify the relative contribution of DOC from wetlands/riparian zones along streams, and off stream forest habitats, respectively. We present data on spatial and temporal variability of DOC concentrations and δ13C-DOC values, during the year of 2005 in Krycklan catchment, a boreal stream network in northern Sweden. Ten stream sites, ranging from order 1 to 4, were monitored in sub catchments with different wetland coverage. Spatial variation of DOC concentration showed a weak but statistically significant relationship with wetland area, with higher concentration with increasing percent of wetland in the drainage area. During base flow the difference in δ13C-DOC values was significantly different between forest (-27.5‰) and wetland (-28.1‰). This spatial pattern disappears during spring peak flow when higher discharge flushing upper soil layer and the riparian zone on DOC in the catchments. A simple mixing model using DOC and δ13C-DOC showed that stream water DOC could be describe as a mixture of DOC coming from forest (deep) groundwater and wetland/riparian zone water. The result indicates that during spring peak flow almost all stream DOC (84-100%) is derived from wetlands and riparian zones. The wetland/riparian water dominates the stream DOC flux at all hydrological events, except for two sites, one forest dominated and one mixed catchment, where the forest groundwater dominated the DOC transport during base flow. Although the total wetland area in Krycklan catchment only represent 8.3%, it contributed, together with riparian zones, to as much as 83% of the yearly DOC transport. This study shows that there is a great potential in using stable carbon isotopes to quantify the relative contribution of DOC from various landscape compartments in catchments. Quantitative patterns are crucial for several reasons. It is for example necessary in predicting the response to global warming which will result in a changed hydrology and shifts in the relative area of the landscape compartments in boreal environments. KEY WORDS carbon isotopes; dissolved organic carbon; streams; boreal; landscape compartments; wetland; groundwater

Influences of organic carbon speciation on hyporheic corridor biogeochemistry and microbial ecology

DOE Office of Scientific and Technical Information (OSTI.GOV)

Stegen, James C.; Johnson, Tim; Fredrickson, James K.

The hyporheic corridor (HC) is a critical component of riverine ecosystems that encompasses the river-11 groundwater continuum. The mixing of groundwater (GW) with river water (RW) in the HC can 12 stimulate biogeochemical activity, and here we (i) propose a novel thermodynamic mechanism 13 underlying this phenomenon, and (ii) reveal broader impacts on dissolved organic carbon (DOC) 14 biogeochemistry and microbial ecology. We show that thermodynamically-favorable DOC 15 accumulates in GW despite decreases in DOC concentration along subsurface flow paths, and that RW 16 contains less thermodynamically-favorable DOC, but at higher concentrations. This indicates that DOC 17 in GW ismore » protected from microbial oxidation by low total energy contained within the DOC pool, while 18 RW DOC is protected by lower thermodynamic favorability of carbon species. We propose that GW-19 RW mixing overcomes these protection mechanisms and stimulates respiration. Mixing models 20 coupled with time-lapse electrical resistance tomography revealed that stimulated respiration leads 21 to tipping points in spatiotemporal dynamics of DOC across the HC. Further, shifts in DOC speciation 22 and biochemical pathways were associated with shifts in microbiome composition, highlighting 23 feedbacks among hydrology, DOC biochemistry, and microbial ecology. These results reveal that 24 previously unrecognized thermodynamic-based mechanisms regulated by GW-RW mixing can strongly 25 influence biogeochemical and microbial dynamics in riverine ecosystems.« less

Influences of organic carbon speciation on hyporheic corridor biogeochemistry and microbial ecology

DOE PAGES

Stegen, James C.; Johnson, Tim; Fredrickson, James K.; ...

2018-02-08

The hyporheic corridor (HC) is a critical component of riverine ecosystems that encompasses the river-11 groundwater continuum. The mixing of groundwater (GW) with river water (RW) in the HC can 12 stimulate biogeochemical activity, and here we (i) propose a novel thermodynamic mechanism 13 underlying this phenomenon, and (ii) reveal broader impacts on dissolved organic carbon (DOC) 14 biogeochemistry and microbial ecology. We show that thermodynamically-favorable DOC 15 accumulates in GW despite decreases in DOC concentration along subsurface flow paths, and that RW 16 contains less thermodynamically-favorable DOC, but at higher concentrations. This indicates that DOC 17 in GW ismore » protected from microbial oxidation by low total energy contained within the DOC pool, while 18 RW DOC is protected by lower thermodynamic favorability of carbon species. We propose that GW-19 RW mixing overcomes these protection mechanisms and stimulates respiration. Mixing models 20 coupled with time-lapse electrical resistance tomography revealed that stimulated respiration leads 21 to tipping points in spatiotemporal dynamics of DOC across the HC. Further, shifts in DOC speciation 22 and biochemical pathways were associated with shifts in microbiome composition, highlighting 23 feedbacks among hydrology, DOC biochemistry, and microbial ecology. These results reveal that 24 previously unrecognized thermodynamic-based mechanisms regulated by GW-RW mixing can strongly 25 influence biogeochemical and microbial dynamics in riverine ecosystems.« less

Seasonal relationships between planktonic microorganisms and dissolved organic material in an alpine stream

USGS Publications Warehouse

McKnight, Diane M.; Smith, R.L.; Harnish, R.A.; Miller, C.L.; Bencala, K.E.

1993-01-01

The relationships between the abundance and activity of planktonic, heterotrophic microorganisms and the quantity and characteristics of dissolved organic carbon (DOC) in a Rocky Mountain stream were evaluated. Peak values of glucose uptake, 2.1 nmol L-1 hr-1, and glucose concentration, 333 nM, occurred during spring snowmelt when the water temperature was 4.0??C and the DOC concentration was greatest. The turnover time of the in situ glucose pool ranged seasonally from 40-1110 hours, with a mean of 272 hr. Seasonal uptake of3H-glucose, particulate ATP concentrations, and direct counts of microbial biomass were independent of temperature, but were positively correlated with DOC concentrations and negatively correlated with stream discharge. Heterotrophic activity in melted snow was generally low, but patchy. In the summer, planktonic heterotrophic activity and microbial biomass exhibited small-scale diel cycles which did not appear to be related to fluctuations in discharge or DOC, but could be related to the activity of benthic invertebrates. Leaf-packs placed under the snow progressively lost weight and leachable organic material during the winter, indicating that the annual litterfall in the watershed may be one source of the spring flush of DOC. These results indicate that the availability of labile DOC to the stream ecosystem is the primary control on seasonal variation in heterotrophic activity of planktonic microbial populations. ?? 1993 Kluwer Academic Publishers.

The physiological response of two green calcifying algae from the Great Barrier Reef towards high dissolved inorganic and organic carbon (DIC and DOC) availability.

PubMed

Meyer, Friedrich Wilhelm; Vogel, Nikolas; Teichberg, Mirta; Uthicke, Sven; Wild, Christian

2015-01-01

Increasing dissolved inorganic carbon (DIC) concentrations associated with ocean acidification can affect marine calcifiers, but local factors, such as high dissolved organic carbon (DOC) concentrations through sewage and algal blooms, may interact with this global factor. For calcifying green algae of the genus Halimeda, a key tropical carbonate producer that often occurs in coral reefs, no studies on these interactions have been reported. These data are however urgently needed to understand future carbonate production. Thus, we investigated the independent and combined effects of DIC (pCO2 402 μatm/ pHtot 8.0 and 996 μatm/ pHtot 7.7) and DOC (added as glucose in 0 and 294 μmol L-1) on growth, calcification and photosynthesis of H. macroloba and H. opuntia from the Great Barrier Reef in an incubation experiment over 16 days. High DIC concentrations significantly reduced dark calcification of H. opuntia by 130 % and led to net dissolution, but did not affect H. macroloba. High DOC concentrations significantly reduced daily oxygen production of H. opuntia and H. macroloba by 78 % and 43 %, respectively, and significantly reduced dark calcification of H. opuntia by 70%. Combined high DIC and DOC did not show any interactive effects for both algae, but revealed additive effects for H. opuntia where the combination of both factors reduced dark calcification by 162 % compared to controls. Such species-specific differences in treatment responses indicate H. opuntia is more susceptible to a combination of high DIC and DOC than H. macroloba. From an ecological perspective, results further suggest a reduction of primary production for Halimeda-dominated benthic reef communities under high DOC concentrations and additional decreases of carbonate accretion under elevated DIC concentrations, where H. opuntia dominates the benthic community. This may reduce biogenic carbonate sedimentation rates and hence the buffering capacity against further ocean acidification.

Nitrogen and carbon dynamics beneath on-site wastewater treatment systems in Pitt County, North Carolina.

PubMed

Del Rosario, Katie L; Humphrey, Charles P; Mitra, Siddhartha; O'Driscoll, Michael A

2014-01-01

On-site wastewater treatment systems (OWS) are a potentially significant non-point source of nutrients to groundwater and surface waters, and are extensively used in coastal North Carolina. The goal of this study was to determine the treatment efficiency of four OWS in reducing total dissolved nitrogen (TDN) and dissolved organic carbon (DOC) concentrations before discharge to groundwater and/or adjacent surface water. Piezometers were installed for groundwater sample collection and nutrient analysis at four separate residences that use OWS. Septic tank effluent, groundwater, and surface water samples (from an adjacent stream) were collected four times during 2012 for TDN and DOC analysis and pH, temperature, electrical conductivity, and dissolved oxygen measurements. Treatment efficiencies from the tank to the groundwater beneath the drainfields ranged from 33 to 95% for TDN and 45 to 82% for DOC, although dilution accounted for most of the concentration reductions. There was a significant positive correlation between nitrate concentration and separation distance from trench bottom to water table and a significant negative correlation between DOC concentration and separation distance. The TDN and DOC transport (>15 m) from two OWS with groundwater saturated drainfield trenches was significant.

Absorption features of chromophoric dissolved organic matter (CDOM) and tracing implication for dissolved organic carbon (DOC) in Changjiang Estuary, China

NASA Astrophysics Data System (ADS)

Zhang, X. Y.; Chen, X.; Deng, H.; Du, Y.; Jin, H. Y.

2013-07-01

Chromophoric dissolved organic matter (CDOM) represents the light absorbing fraction of dissolved organic carbon (DOC). Studies have shown that the optical properties of CDOM can be used to infer the distribution and diffusion characteristics of DOC in the estuary and coastal zone. The inversion of DOC concentrations from remote sensing has been implemented in certain regions. In this study we investigate the potential of tracing DOC from CDOM by the measurement of DOC, absorption spectrum of CDOM, Chla concentration, suspended sediment (SS), and salinity from cruises in different seasons around the Changjiang estuary. Our results show that around the Changjiang estuary the absorption coefficients of CDOM in general have the similar spatial and temporal characteristics as that of DOC, but the strength of the correlation between CDOM and DOC varies locally and seasonally. The input of pollutants from outside the estuary, the bloom of phytoplankton in spring, re-suspension of deposited sediment, and light bleaching all contribute to the local and seasonal variation of the correlation between DOC and CDOM. An inversion model for the determination of DOC from CDOM is established, but the stability of model parameters and its application in different environments need further study. We find that relative to the absorption coefficient of CDOM, the fitted parameters of the absorption spectrum of DOM are better indictors for the composition of DOC. In addition, it is found that the terrestrial input of DOC to Changjiang estuary is a typical two-stage dilution process instead of a linear diffusion process.

Modeling the production, decomposition, and transport of dissolved organic carbon in boreal soils

USGS Publications Warehouse

Fan, Zhaosheng; Neff, Jason C.; Wickland, Kimberly P.

2010-01-01

The movement of dissolved organic carbon (DOC) through boreal ecosystems has drawn increased attention because of its potential impact on the feedback of OC stocks to global environmental change in this region. Few models of boreal DOC exist. Here we present a one-dimensional model with simultaneous production, decomposition, sorption/desorption, and transport of DOC to describe the behavior of DOC in the OC layers above the mineral soils. The field-observed concentration profiles of DOC in two moderately well-drained black spruce forest sites (one with permafrost and one without permafrost), coupled with hourly measured soil temperature and moisture, were used to inversely estimate the unknown parameters associated with the sorption/desorption kinetics using a global optimization strategy. The model, along with the estimated parameters, reasonably reproduces the concentration profiles of DOC and highlights some important potential controls over DOC production and cycling in boreal settings. The values of estimated parameters suggest that humic OC has a larger potential production capacity for DOC than fine OC, and most of the DOC produced from fine OC was associated with instantaneous sorption/desorption whereas most of the DOC produced from humic OC was associated with time-dependent sorption/desorption. The simulated DOC efflux at the bottom of soil OC layers was highly dependent on the component and structure of the OC layers. The DOC efflux was controlled by advection at the site with no humic OC and moist conditions and controlled by diffusion at the site with the presence of humic OC and dry conditions.

Hydrological processes and permafrost regulate magnitude, source and chemical characteristics of dissolved organic carbon export in a peatland catchment of northeastern China

NASA Astrophysics Data System (ADS)

Guo, Yuedong; Song, Changchun; Tan, Wenwen; Wang, Xianwei; Lu, Yongzheng

2018-02-01

Permafrost thawing in peatlands has the potential to alter the catchment export of dissolved organic carbon (DOC), thus influencing the carbon balance and cycling in linked aquatic and ocean ecosystems. Peatlands along the southern margins of the Eurasian permafrost are relatively underexplored despite the considerable risks associated with permafrost degradation due to climate warming. This study examined dynamics of DOC export from a permafrost peatland catchment located in northeastern China during the 2012 to 2014 growing seasons. The estimated annual DOC loads varied greatly between 3211 and 19 022 kg yr-1, with a mean DOC yield of 4.7 g m-2 yr-1. Although the estimated DOC yield was in the lower range compared with other permafrost regions, it was still significant for the net carbon balance in the studied catchment. There were strong linkages between daily discharge and DOC concentrations in both wet and dry years, suggesting a transport-limited process of DOC delivery from the catchment. Discharge explained the majority of both seasonal and interannual variations of DOC concentrations, which made annual discharge a good indicator of total DOC load from the catchment. As indicated by three fluorescence indices, DOC source and chemical characteristics tracked the shift of flow paths during runoff processes closely. Interactions between the flow path and DOC chemical characteristics were greatly influenced by the seasonal thawing of the soil active layer. The deepening of the active layer due to climate warming likely increases the proportion of microbial-originated DOC in baseflow discharge.

On the Use of Ocean Color Remote Sensing to Measure the Transport of Dissolved Organic Carbon by the Mississippi River Plume

NASA Technical Reports Server (NTRS)

DelCastillo, Carlos E.; Miller, Richard L.

2007-01-01

We investigated the use of ocean color remote sensing to measure transport of dissolved organic carbon (DOC) by the Mississippi River to the Gulf of Mexico. From 2000 to 2005 we recorded surface measurements of DOC, colored dissolved organic matter (CDOM), salinity, and water-leaving radiances during five cruises to the Mississippi River Plume. These measurements were used to develop empirical relationships to derive CDOM, DOC, and salinity from monthly composites of SeaWiFS imagery collected from 1998 through 2005. We used river flow data and a two-end-member mixing model to derive DOC concentrations in the river end-member, river flow, and DOC transport using remote sensing data. We compared our remote sensing estimates of river flow and DOC transport with data collected by the United States Geological Survey (USGS) from 1998 through 2005. Our remote sensing estimates of river flow and DOC transport correlated well (r2 0.70) with the USGS data. Our remote sensing estimates and USGS field data showed low variability in DOC concentrations in the river end-member (7-11%), and high seasonal variability in river flow (50%). Therefore, changes in river flow control the variability in DOC transport, indicating that the remote sensing estimate of river flow is the most critical element of our DOC transport measurement. We concluded that it is possible to use this method to estimate DOC transport by other large rivers if there are data on the relationship between CDOM, DOC, and salinity in the river plume.

DOC quantity and quality in northeastern USA catchments

NASA Astrophysics Data System (ADS)

Shanley, J. B.; Sebestyen, S. D.; Aiken, G.; Pellerin, B. A.

2011-12-01

At the Sleepers River Research Watershed in Vermont we have studied interactions of dissolved organic carbon (DOC) cycling and hydrological processes for nearly 20 years to determine how and when DOC is transported through the landscape. Stream DOC concentration in this cool temperate forested catchment varies from ~1 to ~15 mg L-1 and is transport-limited; concentrations increase with increasing flow, even under the wettest conditions, suggesting shifting but non-depletable sources. Specific UV absorbance (SUVA) also increases consistently with flow. Source strength does vary seasonally, however, evidenced by higher DOC for a given flow during autumn leaf fall relative to spring snowmelt. Recent high-frequency optical sensor measurements have revealed fine-scale structure in the temporal DOC pattern not possible from discrete sampling. We observe a consistent counterclockwise hysteresis and diurnal cycles with seasonally variable amplitude. In this presentation we infer DOC sources and processes through analysis of antecedent moisture conditions and concurrent variations in nitrate, dissolved organic nitrogen, and SUVA. With sensors and sampling in place at several other research catchments, we are investigating the similarity of patterns across the northeastern USA.

Chemical and carbon isotopic composition of dissolved organic carbon in a regional confined methanogenic aquifer

USGS Publications Warehouse

Aravena, R.; Wassenaar, L.I.; Spiker, E. C.

2004-01-01

This study demonstrates the advantage of a combined use of chemical and isotopic tools to understand the dissolved organic carbon (DOC) cycle in a regional confined methanogenic aquifer. DOC concentration and carbon isotopic data demonstrate that the soil zone is a primary carbon source of groundwater DOC in areas close to recharge zones. An in-situ DOC source linked to organic rich sediments present in the aquifer matrix is controlling the DOC pool in the central part of the groundwater flow system. DOC fractions, 13C-NMR on fulvic acids and 14C data on DOC and CH4 support the hypothesis that the in-situ DOC source is a terrestrial organic matter and discard the Ordovician bedrock as a source of DOC. ?? 2004 Taylor and Francis Ltd.

Ocean chemistry. Dilution limits dissolved organic carbon utilization in the deep ocean.

PubMed

Arrieta, Jesús M; Mayol, Eva; Hansman, Roberta L; Herndl, Gerhard J; Dittmar, Thorsten; Duarte, Carlos M

2015-04-17

Oceanic dissolved organic carbon (DOC) is the second largest reservoir of organic carbon in the biosphere. About 72% of the global DOC inventory is stored in deep oceanic layers for years to centuries, supporting the current view that it consists of materials resistant to microbial degradation. An alternative hypothesis is that deep-water DOC consists of many different, intrinsically labile compounds at concentrations too low to compensate for the metabolic costs associated to their utilization. Here, we present experimental evidence showing that low concentrations rather than recalcitrance preclude consumption of a substantial fraction of DOC, leading to slow microbial growth in the deep ocean. These findings demonstrate an alternative mechanism for the long-term storage of labile DOC in the deep ocean, which has been hitherto largely ignored. Copyright © 2015, American Association for the Advancement of Science.

Estimating absorption coefficients of colored dissolved organic matter (CDOM) using a semi-analytical algorithm for Southern Beaufort Sea (Canadian Arctic) waters: application to deriving concentrations of dissolved organic carbon from space

NASA Astrophysics Data System (ADS)

Matsuoka, A.; Hooker, S. B.; Bricaud, A.; Gentili, B.; Babin, M.

2012-10-01

A series of papers have suggested that freshwater discharge, including a large amount of dissolved organic matter (DOM), has increased since the middle of the 20th century. In this study, a semi-analytical algorithm for estimating light absorption coefficients of the colored fraction of DOM (CDOM) was developed for Southern Beaufort Sea waters using remote sensing reflectance at six wavelengths in the visible spectral domain corresponding to MODIS ocean color sensor. This algorithm allows to separate colored detrital matter (CDM) into CDOM and non-algal particles (NAP) by determining NAP absorption using an empirical relationship between NAP absorption and particle backscattering coefficients. Evaluation using independent datasets, that were not used for developing the algorithm, showed that CDOM absorption can be estimated accurately to within an uncertainty of 35% and 50% for oceanic and turbid waters, respectively. In situ measurements showed that dissolved organic carbon (DOC) concentrations were tightly correlated with CDOM absorption (r2 = 0.97). By combining the CDOM absorption algorithm together with the DOC versus CDOM relationship, it is now possible to estimate DOC concentrations in the near-surface layer of the Southern Beaufort Sea using satellite ocean color data. DOC concentrations in the surface waters were estimated using MODIS ocean color data, and the estimates showed reasonable values compared to in situ measurements. We propose a routine and near real-time method for deriving DOC concentrations from space, which may open the way to an estimate of DOC budgets for Arctic coastal waters.

Variability of dissolved organic carbon in precipitation during storms at the Shale Hills Critical Zone Observatory

USGS Publications Warehouse

Iavorivska , Lidiia; Boyer, Elizabeth W.; Grimm, Jeffrey W.; Miller, Matthew P.; DeWalle, David R.; Davis, Kenneth J.; Kaye, Margot W.

2017-01-01

Organic compounds are removed from the atmosphere and deposited to the earth's surface via precipitation. In this study, we quantified variations of dissolved organic carbon (DOC) in precipitation during storm events at the Shale Hills Critical Zone Observatory, a forested watershed in central Pennsylvania (USA). Precipitation samples were collected consecutively throughout the storm during 13 events, which spanned a range of seasons and synoptic meteorological conditions, including a hurricane. Further, we explored factors that affect the temporal variability by considering relationships of DOC in precipitation with atmospheric and storm characteristics. Concentrations and chemical composition of DOC changed considerably during storms, with the magnitude of change within individual events being comparable or higher than the range of variation in average event composition among events. While some previous studies observed that concentrations of other elements in precipitation typically decrease over the course of individual storm events, results of this study show that DOC concentrations in precipitation are highly variable. During most storm events concentrations decreased over time, possibly as a result of washing out of the below-cloud atmosphere. However, increasing concentrations that were observed in the later stages of some storm events highlight that DOC removal with precipitation is not merely a dilution response. Increases in DOC during events could result from advection of air masses, local emissions during breaks in precipitation, or chemical transformations in the atmosphere that enhance solubility of organic carbon compounds. This work advances understanding of processes occurring during storms that are relevant to studies of atmospheric chemistry, carbon cycling, and ecosystem responses.

Urbanization Changes the Temporal Dynamics of Nutrients and Water Chemistry

NASA Astrophysics Data System (ADS)

Steele, M.; Badgley, B.

2017-12-01

Recent studies find that urban development alters the seasonal dynamics of nutrient concentrations, where the highest concentrations of nitrogen occurred during the winter in urban watersheds, rather than the summer. However, the effects of urbanization on the seasonal concentrations of other nutrients and chemical components is unknown. Therefore, to determine how urbanization changes the seasonal dynamics, once a week we measured concentrations of dissolved organic carbon (DOC), nutrients (NO3, DON, TN, PO4), base cations (Ca, Mg, Na, K), anions (F, Cl, SO4), pH, sediment, temperature, conductivity, and dissolved oxygen (DO) of nine urban, agricultural, and minimally developed watersheds in southwest Virginia, USA. We found that urbanization disrupted the seasonal dynamics of all metrics, except DON, PO4, Ca, sediment, and DO, where some shifted to high concentrations during the winter (Cl, conductivity), highs during late winter or spring (DOC, Na), a season low (TN, SO4, NO3) or high (NH4) during the summer, or remained more constant throughout the year compared to the reference watersheds (Mg, K, pH). The complex changes in seasonal dynamics coincide with a decoupling of common correlations between constituents; for example, DO and NO3 are negatively correlated in reference watersheds (NO3 increases, DO decreases), but positively correlated in urban watersheds. These results suggest that as watersheds become more intensely developed, the influence of natural drivers like temperature and vegetation become steadily overcome by the influence of urban drivers like deicing salts and wastewater leakage, which exert increasing control of seasonal water quality and aquatic habitat.

Process Inference from High Frequency Temporal Variations in Dissolved Organic Carbon (DOC) Dynamics Across Nested Spatial Scales

NASA Astrophysics Data System (ADS)

Tunaley, C.; Tetzlaff, D.; Lessels, J. S.; Soulsby, C.

2014-12-01

In order to understand aquatic ecosystem functioning it is critical to understand the processes that control the spatial and temporal variations in DOC. DOC concentrations are highly dynamic, however, our understanding at short, high frequency timescales is still limited. Optical sensors which act as a proxy for DOC provide the opportunity to investigate near-continuous DOC variations in order to understand the hydrological and biogeochemical processes that control concentrations at short temporal scales. Here we present inferred 15 minute stream water DOC data for a 12 month period at three nested scales (1km2, 3km2 and 31km2) for the Bruntland Burn, a headwater catchment in NE Scotland. High frequency data were measured using FDOM and CDOM probes which work by measuring the fluorescent component and coloured component, respectively, of DOC when exposed to ultraviolet light. Both FDOM and CDOM were strongly correlated (r2 >0.8) with DOC allowing high frequency estimations. Results show the close coupling of DOC with discharge throughout the sampling period at all three spatial scales. However, analysis at the event scale highlights anticlockwise hysteresis relationships between DOC and discharge due to the delay in DOC being flushed from the increasingly large areas of peaty soils as saturation zones expand and increase hydrological connectivity. Lag times vary between events dependent on antecedent conditions. During a 10 year drought period in late summer 2013 it was apparent that very small changes in discharge on a 15 minute timescale result in high increases in DOC. This suggests transport limitation during this period where DOC builds up in the soil and is not flushed regularly, therefore any subsequent increase in discharge results in large DOC peaks. The high frequency sensors also reveal diurnal variability during summer months related to the photo-oxidation, evaporative and biological influences of DOC during the day. This relationship is less significant during the winter months.

Quantification of Microbial Osmolytes in a Drought Impacted California Grassland

NASA Astrophysics Data System (ADS)

Boot, C. M.; Schaeffer, S. M.; Doyle, A. P.; Schimel, J. P.

2008-12-01

With drought frequency and severity likely increasing in the future, understanding its effect on terrestrial carbon (C) and nitrogen (N) cycling has become essential for accurately modeling ecosystem responses to climate change. Microbes respond to drought stress by accumulating internal solutes, or osmolytes, such as amino acids, betaines and polyols, to balance cell membrane water potential as the soil dries. However, when seasonal rains arrive, internal solutes are released and rapidly mineralized. We have been studying these processes in a California grassland. Beginning in summer 2007, we made monthly measurements of soil moisture, individual amino acid concentration in total soil and in microbial biomass, total dissolved organic carbon and nitrogen (DOC and DON), and microbial biomass carbon and nitrogen (MBC and MBN). We expected microbial concentrations of the known amino acid osmolytes glutamate (glu) and proline (pro) to fluctuate inversely with soil moisture. However, pro was only recovered in Mar 2008 (0.30 μg C g-1 dry soil) and the glu concentration varied proportionally with soil moisture: lowest during summer (0.06 g H2O g-1 dry soil, 2.22 μg glutamate-C g-1 dry soil) and highest in winter (0.27 g H2O g-1 dry soil, 4.43 μg glutamate-C g-1 dry soil). The trend from DOC, MBC, and DON measurements was opposite, however, with all concentrations decreasing as soil moisture shifted from dry to wet, (DOC: 64.61 to 32.49 μg C g-1 dry soil respectively). MBN was the exception to this trend, with concentrations staying nearly constant across seasons. These patterns suggest that the expected amino acids glu and pro are not being used for microbial osmoregulation in the CA grassland, and given the summer to winter decrease in MBC, the primary osmolyte source is likely to be either polyol-type compounds such as mannitol or betaines. The implications for terrestrial carbon cycle are considerable because as the frequency of drought increases, the accumulation and release of osmolytes in response to drought has potential to pump carbon out of the grassland ecosystem.

Carbon export and cycling by the Yukon, Tanana, and Porcupine rivers, Alaska, 2001-2005

USGS Publications Warehouse

Striegl, Robert G.; Dornblaser, Mark M.; Aiken, George R.; Wickland, Kimberly P.; Raymond, Peter A.

2007-01-01

Loads and yields of dissolved and particulate organic and inorganic carbon (DOC, POC, DIC, PIC) were measured and modeled at three locations on the Yukon River (YR) and on the Tanana and Porcupine rivers (TR, PR) in Alaska during 2001–2005. Total YR carbon export averaged 7.8 Tg C yr−1, 30% as OC and 70% as IC. Total C yields (0.39–1.03 mol C m−2 yr−1) were proportional to water yields (139–356 mm yr−1; r2 = 0.84) at all locations. Summer DOC had an aged component (fraction modern (FM) = 0.94–0.97), except in the permafrost wetland‐dominated PR, where DOC was modern. POC had FM = 0.63–0.70. DOC had high concentration, high aromaticity, and high hydrophobic content in spring and low concentration, low aromaticity, and high hydrophilic content in winter. About half of annual DOC export occurred during spring. DIC concentration and isotopic composition were strongly affected by dissolution of suspended carbonates in glacial meltwater during summer.

Spatial and temporal patterns of dissolved organic matter quantity and quality in the Mississippi River Basin, 1997–2013

USGS Publications Warehouse

Stackpoole, Sarah M.; Stets, Edward G.; Clow, David W.; Burns, Douglas A.; Aiken, George R.; Aulenbach, Brent T.; Creed, Irena F.; Hirsch, Robert M.; Laudon, Hjalmar; Pellerin, Brian; Striegl, Robert G.

2017-01-01

Recent studies have found insignificant or decreasing trends in time-series dissolved organic carbon (DOC) datasets, questioning the assumption that long-term DOC concentrations in surface waters are increasing in response to anthropogenic forcing, including climate change, land use, and atmospheric acid deposition. We used the weighted regressions on time, discharge, and season (WRTDS) model to estimate annual flow-normalized concentrations and fluxes to determine if changes in DOC quantity and quality signal anthropogenic forcing at 10 locations in the Mississippi River Basin. Despite increases in agriculture and urban development throughout the basin, net increases in DOC concentration and flux were significant at only 3 of 10 sites from 1997 to 2013 and ranged between −3.5% to +18% and −0.1 to 19%, respectively. Positive shifts in DOC quality, characterized by increasing specific ultraviolet absorbance at 254 nm, ranged between +8% and +45%, but only occurred at one of the sites with significant DOC quantity increases. Basinwide reductions in atmospheric sulfate deposition did not result in large increases in DOC either, likely because of the high buffering capacity of the soil. Hydroclimatic factors including annual discharge, precipitation, and temperature did not significantly change during the 17-year timespan of this study, which contrasts with results from previous studies showing significant increases in precipitation and discharge over a century time scale. Our study also contrasts with those from smaller catchments, which have shown stronger DOC responses to climate, land use, and acidic deposition. This temporal and spatial analysis indicated that there was a potential change in DOC sources in the Mississippi River Basin between 1997 and 2013. However, the overall magnitude of DOC trends was not large, and the pattern in quantity and quality increases for the 10 study sites was not consistent throughout the basin.

Distribution and significance of dissolved organic carbon under three land-use systems, NSW, Australia

NASA Astrophysics Data System (ADS)

Fancy, Rubeca; Wilson, Brian R.; Daniel, Heiko; Osanai, Yui

2017-04-01

Carbon accumulation in surface soils is well documented but very little is known about the mechanisms and processes that result in carbon accumulation and long-term storage in the deeper soil profile. Understanding soil carbon storage and distribution mechanisms is critical to evaluate the sequestration potential of the soils of different land uses. Recent investigations have demonstrated that the movement of dissolved organic carbon (DOC) in the soil profile could contribute significantly to the carbon balance of terrestrial ecosystems. However, very little is known regarding the importance of DOC to vertical distribution of soil organic carbon (SOC) pool through the soil profile in different land-use systems, management practices and conditions prevalent in Australia. We investigated the quantity and distribution of SOC and DOC through the profile under three different land-use systems in northern NSW, Australia. A series of site clusters containing a representative range of land-uses (cultivated, improved pasture and woodland) were selected across the region. Within each land use, we determined SOC and DOC concentration and quantity down the soil profile to a depth of 0-100 cm using six soil depth increments. Here we discuss the distribution and relative importance of DOC down the soil profile to the storage and distribution of carbon. We compare and contrast the patterns associated with the different land use systems and explore potential mechanisms of carbon cycling in these soils. Near to the soil surface, SOC had larger concentrations in the order woodland>improved pasture>cropping at all sites studied. However, DOC was found in significantly larger concentrations in the woodland soils at all soil depths. The larger DOC:TOC ratio in woodland and improved pasture soils suggests a direct relationship between TOC and DOC but increased DOC:TOC ratio in deeper soil layers suggests an increasing importance of DOC in soil carbon cycling in these deeper soils under Australian conditions.

Distributions of nutrients, dissolved organic carbon and carbohydrates in the western Arctic Ocean

NASA Astrophysics Data System (ADS)

Wang, Deli; Henrichs, Susan M.; Guo, Laodong

2006-09-01

Seawater samples were collected from stations along a transect across the shelf-basin interface in the western Arctic Ocean during September 2002, and analyzed for nutrients, dissolved organic carbon (DOC), and total dissolved carbohydrate (TDCHO) constituents, including monosaccharides (MCHO) and polysaccharides (PCHO). Nutrients (nitrate, ammonium, phosphate and dissolved silica) were depleted at the surface, especially nitrate. Their concentrations increased with increasing depth, with maxima centered at ˜125 m depth within the halocline layer, then decreased with increasing depth below the maxima. Both ammonium and phosphate concentrations were elevated in shelf bottom waters, indicating a possible nutrient source from sediments, and in a plume that extended into the upper halocline waters offshore. Concentrations of DOC ranged from 45 to 85 μM and had an inverse correlation with salinity, indicating that mixing is a control on DOC concentrations. Concentrations of TDCHO ranged from 2.5 to 19 μM-C, comprising 13-20% of the bulk DOC. Higher DOC concentrations were found in the upper water column over the shelf along with higher TDCHO concentrations. Within the TDCHO pool, the concentrations of MCHO ranged from 0.4 to 8.6 μM-C, comprising 20-50% of TDCHO, while PCHO concentrations ranged from 0.5 to 13.6 μM-C, comprising 50-80% of the TDCHO. The MCHO/TDCHO ratio was low in the upper 25 m of the water column, followed by a high MCHO/TDCHO ratio between 25 and 100 m, and a low MCHO/TDCHO ratio again below 100 m. The high MCHO/TDCHO ratio within the halocline layer likely resulted from particle decomposition and associated release of MCHO, whereas the low MCHO/TDCHO (or high PCHO/TDCHO) ratio below the halocline layer could have resulted from slow decomposition and additional particulate CHO sources.

Water-Quality Constituents, Dissolved-Organic-Carbon Fractions, and Disinfection By-Product Formation in Water from Community Water-Supply Wells in New Jersey, 1998-99

USGS Publications Warehouse

Hopple, Jessica A.; Barringer, Julia L.; Koleis, Janece

2007-01-01

Water samples were collected from 20 community water-supply wells in New Jersey to assess the chemical quality of the water before and after chlorination, to characterize the types of organic carbon present, and to determine the disinfection by-product formation potential. Water from the selected wells previously had been shown to contain concentrations of dissolved organic carbon (DOC) that were greater than 0.2 mg/L. Of the selected wells, five are completed in unconfined (or semi-confined) glacial-sediment aquifers of the Piedmont and Highlands (New England) Physiographic Provinces, five are completed in unconfined bedrock aquifers of the Piedmont Physiographic Province, and ten are completed in unconsolidated sediments of the Coastal Plain Physiographic Province. Four of the ten wells in the Coastal Plain are completed in confined parts of the aquifers; the other six are in unconfined aquifers. One or more volatile organic compounds (VOCs) were detected in untreated water from all of the 16 wells in unconfined aquifers, some at concentrations greater than maximum contaminant levels. Those compounds detected included aliphatic compounds such as trichloroethylene and 1,1,1-trichloroethane, aromatic compounds such as benzene, the trihalomethane compound, chloroform, and the gasoline additive methyl tert-butyl ether (MTBE). Concentrations of sodium and chloride in water from one well in a bedrock aquifer and sulfate in water from another exceeded New Jersey secondary standards for drinking water. The source of the sulfate was geologic materials, but the sodium and chloride probably were derived from human inputs. DOC fractions were separated by passing water samples through XAD resin columns to determine hydrophobic fractions from hydrophilic fractions. Concentrations of hydrophobic acids were slightly lower than those of combined hydrophilic acids, neutral compounds, and low molecular weight compounds in most samples. Water samples from the 20 wells were adjusted to a pH of 7, dosed with sodium hypochlorite, and incubated for 168 hours (seven days) at 25 ?C to form disinfection by-products (DBPs). Concentrations of the DBPs-trihalomethanes, haloacetic acids, haloacetonitriles, and chlorate-were measured. Concentrations of these compounds, with few exceptions, were higher in water from Coastal Plain wells than from wells in glacial and bedrock aquifers. The organic-carbon fractions were dosed with sodium hypochlorite, incubated for 168 hours at 25 ?C, and analyzed for trihalomethanes, haloacetic acids, haloacetonitriles, and chlorate. Concentrations of trihalomethanes and haloacetic acids were higher in most of the hydrophobic organic-acid fractions than in the hydrophilic fractions, with the highest concentrations in samples from Coastal Plain aquifers. Traces of haloacetonitriles were measured, mostly in the hydrophilic fraction. The aromaticity of the precursor DOC, as estimated by measurements of the absorbance of ultraviolet light at 254 nanometers, apparently is a factor in the DBP formation potentials determined, as aromaticity was greater in the samples that developed high concentrations of DBPs. VOCs may have contributed to the organic carbon present in some of the samples, but much of the DOC present in water from the 20 wells appeared to be natural in origin. The sediments of the Coastal Plain aquifers, in particular, contain substantial amounts of organic matter, which contribute ammonia, organic nitrogen, and aromatic DOC compounds to the ground water. Thus, the geologic characteristics of the aquifers appear to be a major factor in the potential for ground water to form DBPs when chlorinated.

Development of a combined isotopic and mass-balance approach to determine dissolved organic carbon sources in eutrophic reservoirs.

PubMed

Pierson-Wickmann, Anne-Catherine; Gruau, Gérard; Jardé, Emilie; Gaury, Nicolas; Brient, Luc; Lengronne, Marion; Crocq, André; Helle, Daniel; Lambert, Thibault

2011-04-01

A combined mass-balance and stable isotope approach was set up to identify and quantify dissolved organic carbon (DOC) sources in a DOC-rich (9mgL(-1)) eutrophic reservoir located in Western France and used for drinking water supply (so-called Rophemel reservoir). The mass-balance approach consisted in measuring the flux of allochthonous DOC on a daily basis, and in comparing it with the effective (measured) DOC concentration of the reservoir. The isotopic approach consisted, for its part, in measuring the carbon isotope ratios (δ(13)C values) of both allochthonous and autochthonous DOC sources, and comparing these values with the δ(13)C values of the reservoir DOC. Results from both approaches were consistent pointing out for a DOC of 100% allochthonous origin. In particular, the δ(13)C values of the DOC recovered in the reservoir (-28.5±0.2‰; n=22) during the algal bloom season (May-September) showed no trace of an autochthonous contribution (δ(13)C in algae=-30.1±0.3‰; n=2) being indistinguishable from the δ(13)C values of allochthonous DOC from inflowing rivers (-28.6±0.1‰; n=8). These results demonstrate that eutrophication is not responsible for the high DOC concentrations observed in the Rophemel reservoir and that limiting eutrophication of this reservoir will not reduce the potential formation of disinfection by-products during water treatment. The methodology developed in this study based on a complementary isotopic and mass-balance approach provides a powerful tool, suitable to identify and quantify DOC sources in eutrophic, DOC-contaminated reservoirs. Copyright © 2010 Elsevier Ltd. All rights reserved.

Near-surface Heating of Young Rift Sediment Causes Mass Production and Discharge of Reactive Dissolved Organic Matter

PubMed Central

Lin, Yu-Shih; Koch, Boris P.; Feseker, Tomas; Ziervogel, Kai; Goldhammer, Tobias; Schmidt, Frauke; Witt, Matthias; Kellermann, Matthias Y.; Zabel, Matthias; Teske, Andreas; Hinrichs, Kai-Uwe

2017-01-01

Ocean margin sediments have been considered as important sources of dissolved organic carbon (DOC) to the deep ocean, yet the contribution from advective settings has just started to be acknowledged. Here we present evidence showing that near-surface heating of sediment in the Guaymas Basin, a young extensional depression, causes mass production and discharge of reactive dissolved organic matter (DOM). In the sediment heated up to ~100 °C, we found unexpectedly low DOC concentrations in the pore waters, reflecting the combined effect of thermal desorption and advective fluid flow. Heating experiments suggested DOC production to be a rapid, abiotic process with the DOC concentration increasing exponentially with temperature. The high proportions of total hydrolyzable amino acids and presence of chemical species affiliated with activated hydrocarbons, carbohydrates and peptides indicate high reactivity of the DOM. Model simulation suggests that at the local scale, near-surface heating of sediment creates short and massive DOC discharge events that elevate the bottom-water DOC concentration. Because of the heterogeneous distribution of high heat flow areas, the expulsion of reactive DOM is spotty at any given time. We conclude that hydrothermal heating of young rift sediments alter deep-ocean budgets of bioavailable DOM, creating organic-rich habitats for benthic life. PMID:28327661

Use of induced fluorescence measurements to assess aluminum-organic interactions in acidified lakes

NASA Technical Reports Server (NTRS)

Vodacek, A.; Philpot, W. D.

1985-01-01

The application of laser fluorosensing to the tracing of metals in acid lakes is proposed. The effects of the metals on the dissolving organic carbon (DOC) fluorescence is studied using laboratory mixed water samples and natural water samples from Hamilton and Big Moose Lakes in New York. The operation of the laser fluorosensing system employed in the experiment is described. The DOC fluorescence was quenched by Al, Cu, and Fe, and the relation between pH and the quenching rate is examined. The humic substances fluorescence spectra are analyzed to estimate the concentrations of DOC in water and the relative concentration of Al. The interference problems caused by chemical competition between metal ions and ligands, and changes in the background DOC fluorescence are discussed. It is noted that an airborne laser fluorescence is useful for detecting elevated concentrations of metals.

Seasonal and spatial variation in soil chemistry and anaerobic processes in an Arctic ecosystem

NASA Astrophysics Data System (ADS)

Lipson, D.; Mauritz, M.; Bozzolo, F.; Raab, T. K.; Santos, M. J.; Friedman, E. F.; Rosenbaum, M.; Angenent, L.

2009-12-01

Drained thaw lake basins (DTLB) are the dominant landform in the Arctic coastal plain near Barrow, Alaska. Our previous work in a DTLB showed that Fe(III) and humic substances are important electron acceptors in anaerobic respiration, and play a significant role in the C cycle of these organic-rich soils. In the current study, we investigated seasonal and spatial patterns of availability of electron acceptors and labile substrate, redox conditions and microbial activity. Landscapes within DTLB contain complex, fine-scale topography arising from ice wedge polygons, which produce raised and lowered areas. One goal of our study was to determine the effects of microtopographic variation on the potential for Fe(III) reduction and other anaerobic processes. Additionally, the soil in the study site has a complex vertical structure, with an organic peat layer overlying a mineral layer, overlying permafrost. We described variations in soil chemistry across depth profiles into the permafrost. Finally, we installed an integrated electrode/potentiostat system to electrochemically monitor microbial activity in the soil. Topographically low areas differed from high areas in most of the measured variables: low areas had lower oxidation-reduction potential, higher pH and electrical conductivity. Soil pore water from low areas had higher concentrations of Fe(III), Fe(II), dissolved organic C (DOC), and aromaticity (UV absorbance at 260nm, “A260”). Low areas also had higher concentrations of dissolve CO2 and CH4 in soil pore water. Laboratory incubations of soil showed a trend toward higher potentials for Fe(III) reduction in topographically low areas. Clearly, ice wedge-induced microtopography exerts a strong control on microbial processes in this DTLB landscape, with increased anaerobic activity occurring in the wetter, depressed areas. Soil water extracted from 5-15 cm depth had higher concentrations of Fe(III), Fe(II), A260, and DOC compared to soil water sampled from 0-5cm. The soil depth profile showed highest concentrations of acid-extractable Fe in the mineral layer and permafrost, though Fe(III) was highest in the surface layer. Total and soluble C increased with depth, as did the potential for CO2 and CH4 production in anaerobic incubations. Thus, the mineral layer may be a significant source of Fe for oxidation-reduction reactions that occur at shallower depths, though methanogenesis dominates in the mineral layer, while Fe(III) reduction dominates in the organic layer. Most of the ions measured in the soil pore water (Fe(III), DOC, A260) showed the same general seasonal pattern: high concentrations soon after soils thawed, declining over time until mid-August. Concentrations of Fe(II) in soil pore water were fairly stable over time. There was a significant positive relationship between A260 and Fe(III) concentrations, possibly indicating the presence of microbially-produced aromatic chelating molecules. Potentiostat measurements confirmed the presence of an electrochemically active microbial community in the soil.

Hydrological mobilization of mercury and dissolved organic carbon in a snow-dominated, forested watershed: Conceptualization and modeling

USGS Publications Warehouse

Schelker, J.; Burns, Douglas A.; Weiler, M.; Laudon, H.

2011-01-01

The mobilization of mercury and dissolved organic carbon (DOC) during snowmelt often accounts for a major fraction of the annual loads. We studied the role of hydrological connectivity of riparian wetlands and upland/wetland transition zones to surface waters on the mobilization of Hg and DOC in Fishing Brook, a headwater of the Adirondack Mountains, New York. Stream water total mercury (THg) concentrations varied strongly (mean = 2.25 ?? 0.5 ng L -1), and the two snowmelt seasons contributed 40% (2007) and 48% (2008) of the annual load. Methyl mercury (MeHg) concentrations ranged up to 0.26 ng L-1, and showed an inverse log relationship with discharge. TOPMODEL-simulated saturated area corresponded well with wetland areas, and the application of a flow algorithm based elevation-above-creek approach suggests that most wetlands become well connected during high flow. The dynamics of simulated saturated area and soil storage deficit were able to explain a large part of the variation of THg concentrations (r2 = 0.53 to 0.72). In contrast, the simulations were not able to explain DOC variations and DOC and THg concentrations were not correlated. These results indicate that all three constituents, THg, MeHg, and DOC, follow different patterns at the outlet: (1) the mobilization of THg is primarily controlled by the saturation state of the catchment, (2) the dilution of MeHg suggests flushing from a supply limited pool, and (3) DOC dynamics follow a pattern different from THg dynamics, which likely results from differing gain and/or loss processes for THg and/or DOC within the Fishing Brook catchment. Copyright 2011 by the American Geophysical Union.

An overview of dissolved organic carbon in groundwater and implications for drinking water safety

NASA Astrophysics Data System (ADS)

Regan, S.; Hynds, P.; Flynn, R.

2017-06-01

Dissolved organic carbon (DOC) is composed of a diverse array of compounds, predominantly humic substances, and is a near ubiquitous component of natural groundwater, notwithstanding climatic extremes such as arid and hyper-arid settings. Despite being a frequently measured parameter of groundwater quality, the complexity of DOC composition and reaction behaviour means that links between concentration and human health risk are difficult to quantify and few examples are reported in the literature. Measured concentrations from natural/unpolluted groundwater are typically below 4 mg C/l, whilst concentrations above these levels generally indicate anthropogenic influences and/or contamination issues and can potentially compromise water safety. Treatment processes are effective at reducing DOC concentrations, but refractory humic substance reaction with chlorine during the disinfection process produces suspected carcinogenic disinfectant by-products (DBPs). However, despite engineered artificial recharge systems being commonly used to remove DOC from recycled treated wastewaters, little research has been conducted on the presence of DBPs in potable groundwater systems. In recent years, the capacity to measure the influence of organic matter on colloidal contaminants and its influence on the mobility of pathogenic microorganisms has aided understanding of transport processes in aquifers. Additionally, advances in polymerase chain reaction techniques used for the detection, identification, and quantification of waterborne pathogens, provide a method to confidently investigate the behaviour of DOC and its effect on contaminant transfer in aquifers. This paper provides a summary of DOC occurrence in groundwater bodies and associated issues capable of indirectly affecting human health.

Atmospheric inputs of organic matter to a forested watershed: Variations from storm to storm over the seasons

NASA Astrophysics Data System (ADS)

Iavorivska, Lidiia; Boyer, Elizabeth W.; Miller, Matthew P.; Brown, Michael G.; Vasilopoulos, Terrie; Fuentes, Jose D.; Duffy, Christopher J.

2016-12-01

The objectives of this study were to determine the quantity and chemical composition of precipitation inputs of dissolved organic carbon (DOC) to a forested watershed; and to characterize the associated temporal variability. We sampled most precipitation that occurred from May 2012 through August 2013 at the Susquehanna Shale Hills Critical Zone Observatory (Pennsylvania, USA). Sub-event precipitation samples (159) were collected sequentially during 90 events; covering various types of synoptic meteorological conditions in all climatic seasons. Precipitation DOC concentrations and rates of wet atmospheric DOC deposition were highly variable from storm to storm, ranging from 0.3 to 5.6 mg C L-1 and from 0.5 to 32.8 mg C m-2 h-1, respectively. Seasonally, storms in spring and summer had higher concentrations of DOC and more optically active organic matter than in winter. Higher DOC concentrations resulted from weather types that favor air advection, where cold frontal systems, on average, delivered more than warm/stationary fronts and northeasters. A mixed modeling statistical approach revealed that factors related to storm properties, emission sources, and to the chemical composition of the atmosphere could explain more than 60% of the storm to storm variability in DOC concentrations. This study provided observations on changes in dissolved organic matter that can be useful in modeling of atmospheric oxidative chemistry, exploring relationships between organics and other elements of precipitation chemistry, and in considering temporal changes in ecosystem nutrient balances and microbial activity.

Multi-Ecosystem Assessment of Mercury Bioaccumulation in Fishes: Habitat, Landscape, and Biogeochemical Drivers of Fish Mercury

NASA Astrophysics Data System (ADS)

Eagles-Smith, C.; Ackerman, J.; Herring, G.; Willacker, J.; Flanagan, C.

2014-12-01

Mercury (Hg) is a globally distributed contaminant that threatens ecosystem health across aquatic environments. The complexity of the Hg cycle and its primary drivers, coupled with dynamic food web processes that govern biomagnification, result in marked spatial variability in Hg bioaccumulation across aquatic ecosystems. However, it is unclear if patterns of bioaccumulation are consistent in magnitude and direction across ecosystem types. We synthesized data from several studies spanning more than 200 individual sites, comprising four distinct ecosystem classifications (estuaries, sub-alpine lakes, rivers, and managed wetlands). Within each ecosystem, we compared fish Hg concentrations among replicated sub-habitats and also evaluated the influence of land use, landscape composition, and biogeochemical drivers on fish Hg concentrations. We found substantial variability in fish Hg concentrations among adjacent sub-habitats within ecosystems. In estuarine environments, fish Hg concentrations were 7.4x higher in seasonal-saline wetlands than adjacent tidal wetland habitats. In riverine alcoves, preliminary data suggest that fish Hg concentrations were 1.5x higher than in fishes from paired mainstem river habitat. Among managed wetland habitats, fish Hg concentrations in rice fields were 2x higher than those in managed seasonal wetlands that were subjected to identical wetting and drying patterns. Across ecosystems, dissolved organic carbon (DOC) concentrations in surface waters were consistently correlated with fish Hg concentrations, highlighting its importance in Hg methylation and transport processes. Yet, the strength and direction of the relationships varied among habitat types. For example, fish Hg concentrations were positively correlated with DOC concentrations in riverine environments, whereas we found a negative correlation in alpine lakes. Instead, the most important determinant of fish Hg concentrations in alpine lakes was conifer tree density within a lake's catchment, resulting in a 4x increase in fish Hg concentration in lakes with the lowest to the highest catchment conifer tree density. Together, this integrated ecosystem analysis highlights the importance of understanding small-scale variation in bioaccumulation processes in order to better predict Hg risk.

Habitat, not resource availability, limits consumer production in lake ecosystems

USGS Publications Warehouse

Craig, Nicola; Jones, Stuart E.; Weidel, Brian C.; Solomon, Christopher T.

2015-01-01

Food web productivity in lakes can be limited by dissolved organic carbon (DOC), which reduces fish production by limiting the abundance of their zoobenthic prey. We demonstrate that in a set of 10 small, north temperate lakes spanning a wide DOC gradient, these negative effects of high DOC concentrations on zoobenthos production are driven primarily by availability of warm, well-oxygenated habitat, rather than by light limitation of benthic primary production as previously proposed. There was no significant effect of benthic primary production on zoobenthos production after controlling for oxygen, even though stable isotope analysis indicated that zoobenthos do use this resource. Mean whole-lake zoobenthos production was lower in high-DOC lakes with reduced availability of oxygenated habitat, as was fish biomass. These insights improve understanding of lake food webs and inform management in the face of spatial variability and ongoing temporal change in lake DOC concentrations.

Organic Geochemistry and Sources of Natural Aquatic Foams

USGS Publications Warehouse

Mills, M.S.; Thurman, E.M.; Ertel, J.; Thorn, K.A.

1996-01-01

Aquatic foams and stream-water samples were collected from two pristine sites for humic substances isolation and characterization. Biomarker compounds identified in foam and stream humic substances included phospholipid fatty acids, steroids, and lignin. Results showed that foams had a 10 to 20 fold greater DOC concentration and were enriched in humic substances (90% by weight of DOC) that showed increased hydrophobicity, aliphatic character, and compositional complexity compared to host stream humic substances (55 to 81% by weight of DOC). Foam humic substances also were enriched in humic acid (36 to 83% by weight) compared to host stream humic substances (10 to 14% by weight). Biomarkers, which contributed less than 5% by weight to the DOC pool, indicated higher plants, bacteria, algae, fungi, and diatoms as DOC sources. It is proposed that aquatic foams may be important media for the concentration and transport of organic substances in the aquatic environment.

The influence of dissolved organic carbon on bacterial phosphorus uptake and bacteria-phytoplankton dynamics in two Minnesota lakes

USGS Publications Warehouse

Stets, E.G.; Cotner, J.B.

2008-01-01

The balance of production in any ecosystem is dependent on the flow of limiting nutrients into either the autotrophic or heterotrophic components of the food web. To understand one of the important controls on the flow of inorganic nutrients between phytoplankton and bacterioplankton in lakes, we manipulated dissolved organic carbon (DOC) in two lakes of different trophic status. We hypothesized that labile DOC additions would increase bacterial phosphorus (P) uptake and decrease the response of phytoplankton to nutrient additions. Supplemental nutrients and carbon (C), nitrogen (N, 1.6 ??mol NH4Cl L-1 d-1), P (0.1 ??mol KH 2PO4 L-1 d-1), and DOC (glucose, 15 ??mol C L-1 d-1) were added twice daily to 8-liter experimental units. We tested the effect of added DOC on chlorophyll concentration, bacterial production, biomass, and P uptake using size-fractionated 33P-PO4 uptake. In the oligotrophic lake, DOC additions stimulated bacterial production and increased bacterial biomass-specific P uptake. Bacteria consumed added DOC, and chlorophyll concentrations were significantly lower in carboys receiving DOC additions. In the eutrophic lake, DOC additions had less of a stimulatory effect on bacterial production and biomass-specific P uptake. DOC accumulated over the time period, and there was little evidence for a DOC-induced decrease in phytoplankton biomass. Bacterial growth approached the calculated ??max and yet did not accumulate biomass, indicating significant biomass losses, which may have constrained bacterial DOC consumption. Excess bacterial DOC consumption in oligotrophic lakes may result in greater bacterial P affinity and enhanced nutrient uptake by the heterotrophic compartment of the food web. On the other hand, constraints on bacterial biomass accumulation in eutrophic lakes, from either viral lysis or bacterial grazing, can allow labile DOC to accumulate, thereby negating the effect of excess DOC on the planktonic food web. ?? 2008, by the American Society of Limnology and Oceanography, Inc.

Oxygen dynamics in a boreal lake responds to long-term changes in climate, ice phenology, and DOC inputs

NASA Astrophysics Data System (ADS)

Couture, Raoul-Marie; de Wit, Heleen A.; Tominaga, Koji; Kiuru, Petri; Markelov, Igor

2015-11-01

Boreal lakes are impacted by climate change, reduced acid deposition, and changing loads of dissolved organic carbon (DOC) from catchments. We explored, using the process-based lake model MyLake, how changes in these pressures modulate ice phenology and the dissolved oxygen concentrations (DO) of a small boreal humic lake. The model was parametrized against year-round time series of water temperature and DO from a lake buoy. Observed trends in air temperature (+0.045°C yr-1) and DOC concentration (0.11 mg C L-1 yr-1, +1% annually) over the past 40 years were used as model forcings. A backcast of ice freezing and breakup dates revealed that ice breakup occurred on average 8 days earlier in 2014 than in 1974. The earlier ice breakup enhanced water column ventilation resulting in higher DO in the spring. Warmer water in late summer led to longer anoxic periods, as microbial DOC turnover increased. A long-term increase in DOC concentrations caused a decline in lake DO, leading to 15% more hypoxic days (<3 mg L-1) and 10% more anoxic days (<15 µg L-1) in 2014 than in 1974. We conclude that climate warming and increasing DOC loads are antagonistic with respect to their effect on DO availability. The model suggests that DOC is a stronger driver of DO consumption than temperature. The browning of lakes may thus cause reductions in the oxythermal habitat of fish and aquatic biota in boreal lakes.

Rapid Permafrost Carbon Degradation at the Land-Ocean Interface

NASA Astrophysics Data System (ADS)

Tanski, G.

2015-12-01

Climate change has a strong impact on permafrost coasts in the Arctic. With increasing air and water temperatures, the ice-rich unlithified permafrost coasts will thaw and erode at a greater pace. Organic carbon that has been stored for thousands of years is mobilized and degrades on its way to the ocean. The objective of this study is to investigate to what extent permafrost carbon degrades after thawing before it enters the ocean in a retrogressive thaw slump. A slump located on Herschel Island (Yukon Territory, Canada) was sampled systematically along transects from the permafrost headwall to the coastline. Concentrations of particulate and dissolved organic carbon (POC and DOC) as well as its stable carbon isotopes (δ13C-POC and δ13C-DOC) were measured and compared in frozen deposits and in thawed sediments. Ammonium, nitrite and nitrate were also analyzed in order to identify and understand the carbon metabolization mechanisms taking place during slump activity. Our results show that major portions of permafrost carbon are metabolized right after thawing. Ammonium concentrations are highest in areas where thawed permafrost material directly accumulates. We suggest that before entering the nearshore zone permafrost organic carbon and nitrogen is subject to major degradation and metabolization. This makes permafrost coasts and retrogressive thaw slumps degradation hotspots at the land-ocean-interface.

A novel approach combining self-organizing map and parallel factor analysis for monitoring water quality of watersheds under non-point source pollution

PubMed Central

Zhang, Yixiang; Liang, Xinqiang; Wang, Zhibo; Xu, Lixian

2015-01-01

High content of organic matter in the downstream of watersheds underscored the severity of non-point source (NPS) pollution. The major objectives of this study were to characterize and quantify dissolved organic matter (DOM) in watersheds affected by NPS pollution, and to apply self-organizing map (SOM) and parallel factor analysis (PARAFAC) to assess fluorescence properties as proxy indicators for NPS pollution and labor-intensive routine water quality indicators. Water from upstreams and downstreams was sampled to measure dissolved organic carbon (DOC) concentrations and excitation-emission matrix (EEM). Five fluorescence components were modeled with PARAFAC. The regression analysis between PARAFAC intensities (Fmax) and raw EEM measurements indicated that several raw fluorescence measurements at target excitation-emission wavelength region could provide similar DOM information to massive EEM measurements combined with PARAFAC. Regression analysis between DOC concentration and raw EEM measurements suggested that some regions in raw EEM could be used as surrogates for labor-intensive routine indicators. SOM can be used to visualize the occurrence of pollution. Relationship between DOC concentration and PARAFAC components analyzed with SOM suggested that PARAFAC component 2 might be the major part of bulk DOC and could be recognized as a proxy indicator to predict the DOC concentration. PMID:26526140

Quantifying tropical peatland dissolved organic carbon (DOC) using UV-visible spectroscopy.

PubMed

Cook, Sarah; Peacock, Mike; Evans, Chris D; Page, Susan E; Whelan, Mick J; Gauci, Vincent; Kho, Lip Khoon

2017-05-15

UV-visible spectroscopy has been shown to be a useful technique for determining dissolved organic carbon (DOC) concentrations. However, at present we are unaware of any studies in the literature that have investigated the suitability of this approach for tropical DOC water samples from any tropical peatlands, although some work has been performed in other tropical environments. We used water samples from two oil palm estates in Sarawak, Malaysia to: i) investigate the suitability of both single and two-wavelength proxies for tropical DOC determination; ii) develop a calibration dataset and set of parameters to calculate DOC concentrations indirectly; iii) provide tropical researchers with guidance on the best spectrophotometric approaches to use in future analyses of DOC. Both single and two-wavelength model approaches performed well with no one model significantly outperforming the other. The predictive ability of the models suggests that UV-visible spectroscopy is both a viable and low cost method for rapidly analyzing DOC in water samples immediately post-collection, which can be important when working at remote field sites with access to only basic laboratory facilities. Copyright © 2017 The Authors. Published by Elsevier Ltd.. All rights reserved.

Winter Ground Temperatures Control Snowmelt DOC Export From a Discontinuous Permafrost Watershed: A Multi-Year Perspective

NASA Astrophysics Data System (ADS)

Carey, S. K.

2006-12-01

For discontinuous and continuous permafrost watersheds, the largest mass flux of dissolved organic carbon (DOC) occurs during the snowmelt period. During this time, available allochtonous organic carbon that has accumulated over the winter in frozen organic soils is rapidly flushed to the basin outlet. While this process has been observed now in many river systems of different size and location, there have been few inter-annual reports on the mass of DOC loss and the factors controlling its variability during freshet. Hydrological and DOC fluxes were recorded for the 2002, 2003 and 2006 snowmelt season with supplementary over-winter data for an 8 square kilometer sub-basin (Granger Basin) of the Wolf Creek Research Basin, Yukon Territory, Canada. Granger Basin is an alpine catchment above treeline underlain with discontinuous permafrost (approximately 70 %) and has widespread surface organic soils up to 0.4 m in thickness. Pre-melt snow water equivalent varied widely throughout the basin, yet was greatest in 2006, followed by 2002 and 2003. Ground temperatures were notably colder throughout the 2003 winter compared with 2006 and 2002. For all years, discharge began in mid-May, and was a continuous event in 2002 and 2006. In 2003 four distinct melt-periods were observed due to rising and falling temperatures. During freshet, stream DOC concentration increased rapidly from < 2 mg C/L to > 15 mg C/L on the first ascending limb of the hydrograph in each year. In 2003, DOC was largely flushed from the catchment several weeks prior to peak freshet. DOC concentration in wells and piezometers followed a similar pattern to streamflow DOC, with 2003 groundwater DOC concentrations less than 2002 and 2006. The total mass flux of DOC during freshet was 0.85, 0.45 and 1.01 g C/m2 for 2002, 2003 and 2006 respectively. Despite differences in pre-melt snow accumulation, the timing of melt and the volume of discharge, it appears that spring DOC export is largely controlled by over-winter ground temperatures. This has important implications for carbon mass balances as warming temperatures in the pan-arctic are largely occurring during the winter months.

Application of a UV-Vis submersible probe for capturing changes in DOC concentrations across a mire complex during the snowmelt and summer periods

NASA Astrophysics Data System (ADS)

Avagyan, Armine; Runkle, Benjamin; Kutzbach, Lars

2013-04-01

An accurate quantification of dissolved organic carbon (DOC) is crucial for understanding changes in water resources under the influence of climate, land use and urbanization. However, the conventionally used methods do not allow high frequency in situ analyses in remote or hostile environments (e.g., industrial wastewater or during environmental high-flow events, such as snowmelt or floods). In particular, missing measurements during the snowmelt period in landscapes of the boreal region can lead to significant miscalculations in regional carbon budgets. Therefore, the aim of the study was to test the performance of a portable, submersible UV-Vis spectrophotometer (spectro::lyser, s::can Messtechnik GmbH, Austria) during the snowmelt period in a boreal mire-forest catchment, and to provide a conceptual understanding of the spatial and temporal dynamics of DOC concentrations during and after snowmelt. During 2011, water samples were collected from the near-pristine Ust-Pojeg mire complex in northwestern Russia (61° 56'N, 50° 13'E). Sampling started during the spring snowmelt period and continued until late fall. The mire presented a mosaic of different landscape units. The mire consisted of minerogeous (fen), ombrogenous (bog), and transitional forest-mire (lagg) zones. Water samples were taken from the surface across the mire (22 points at 50-m intervals). DOC concentrations were analyzed directly at the study site using a portable, submersible UV-Vis spectrophotometer, which uses high-resolution absorbance measurements over the wavelength range 200-742.5 nm at 2.5-nm intervals as a proxy for DOC content. Because the DOC composition of fluids varies by site, a local calibration replaced the default settings of the spectro::lyser (Global Calibration) to enhance the accuracy of the measurements. To evaluate the local calibration and correct for drift, the same samples (n = 157) were additionally analyzed using the wet persulfate oxidation method (O-I-Analytica, Aurora Model 1030, USA). Based on ordinary least squares regression, the local calibration showed good agreement between the results obtained from the high-resolution absorption measurements and the wet persulfate oxidation method (r2= 0.99, root-mean-square error = 1.7 mg L-1). The measurement campaign revealed spatial and temporal variability of DOC concentrations, and demonstrated that at the beginning of the snowmelt period, surface carbon was flushed away by meltwater, whereas deeper layers remained frozen. During this time, the surface DOC concentrations fluctuated within the range of 8-15 mg L-1 (April 07) across the entire mire complex. After April 18, the concentrations diverged between the sites; the DOC concentration reached 30 mg L-1in the surface water at the lagg zone but was 15 mg L-1 at the bog site (April 25). The DOC surface water concentration continued to increase during summer and fall, ranging from 19 to 74 mg L-1 across the mire, with an average of 45 ± 14 mg L-1. The study indicates that high-resolution spectroscopic measurements provide a simple, fast, robust and non-destructive method for measuring DOC contents, with a short duration (17-20 seconds) and portability of the sample analysis rendering this method particularly advantageous for in-situ measurements at remote field locations.

Inverse coupling of DOC and nitrate export from soils and streams

NASA Astrophysics Data System (ADS)

Goodale, Christine

2013-04-01

Over the last two decades, nitrate concentrations in surface waters have decreased across the Northeastern United States and parts of northern Europe. Many hypotheses have been proposed to explain this decrease, but the cause remains unclear. One control may be associated with increasing abundance of dissolved organic carbon (DOC), which in turn may be a result of soil recovery from acidification. Compared across catchments, surface water NO3- decreases sharply with increasing DOC concentration. Here, we used measurements of soil and solution nitrate, DOC, and their isotopic composition (13C-DOC, 15N- and 18O-NO3) to test several related hypotheses that changing acidification affects the release of DOC and bio-available DOC (bDOC) from soil, and that variation in stocks of soil C and release of bDOC partly control NO3- export from forested catchments in New York State, USA. We examined whether DOC and NO3- are both driven by soil C processes that produce inverse coupling at the scale of soil cores as well as across catchments, through comparison of soil and surface water chemistry across nine catchments selected from long-term monitoring networks in the Catskill and Adirondack Mountains. In addition, we conducted a series of soil core leaching experiments to examine the role of acidification and recovery in driving the net production of DOC and NO3- from soils. Over 8 months, soil cores were leached biweekly with simulated rainfall solutions of varying pH (3.6 to 7.0) from additions of H2SO4, CaCO3 and NaOH. These experiments did not yield a pH-induced change in DOC quantity, but did show a change in DOC quality, in that acidified cores released more bio-available DOC with less depleted 13C-DOC than cores with experimentally increased pH. All cores leached substantial amounts of nitrate. Together, these lab- and field comparisons are being used to identify the role of soil production and consumption processes in driving cross-watershed differences in DOC and NO3- loss, or whether other factors (e.g., riparian, in-stream or hydrologic processes) likely explain this relationship.

Estimating absorption coefficients of colored dissolved organic matter (CDOM) using a semi-analytical algorithm for southern Beaufort Sea waters: application to deriving concentrations of dissolved organic carbon from space

NASA Astrophysics Data System (ADS)

Matsuoka, A.; Hooker, S. B.; Bricaud, A.; Gentili, B.; Babin, M.

2013-02-01

A series of papers have suggested that freshwater discharge, including a large amount of dissolved organic matter (DOM), has increased since the middle of the 20th century. In this study, a semi-analytical algorithm for estimating light absorption coefficients of the colored fraction of DOM (CDOM) was developed for southern Beaufort Sea waters using remote sensing reflectance at six wavelengths in the visible spectral domain corresponding to MODIS ocean color sensor. This algorithm allows the separation of colored detrital matter (CDM) into CDOM and non-algal particles (NAP) through the determination of NAP absorption using an empirical relationship between NAP absorption and particle backscattering coefficients. Evaluation using independent datasets, which were not used for developing the algorithm, showed that CDOM absorption can be estimated accurately to within an uncertainty of 35% and 50% for oceanic and coastal waters, respectively. A previous paper (Matsuoka et al., 2012) showed that dissolved organic carbon (DOC) concentrations were tightly correlated with CDOM absorption in our study area (r2 = 0.97). By combining the CDOM absorption algorithm together with the DOC versus CDOM relationship, it is now possible to estimate DOC concentrations in the near-surface layer of the southern Beaufort Sea using satellite ocean color data. DOC concentrations in the surface waters were estimated using MODIS ocean color data, and the estimates showed reasonable values compared to in situ measurements. We propose a routine and near real-time method for deriving DOC concentrations from space, which may open the way to an estimate of DOC budgets for Arctic coastal waters.

Long-term decomposition of DOC from experimental diatom blooms

DOE Office of Scientific and Technical Information (OSTI.GOV)

Fry, B.; Hopkinson, C.S. Jr.; Nolin, A.

1996-09-01

Decomposition of {sup 13}C-labeled dissolved organic carbon (DOC) produced in two marine diatom blooms was followed for 2.5 yr with large volume (20 liter) incubations performed in the dark. The {sup 13}C tracer was used to partition decomposition dynamics of the fresh diatom-derived DOC and the turnover of background DOC from Woods Hole Harbor. DOC from Woods Hole harbor proved largely refractory, with DOC concentrations falling from 122 to {approximately} 100 {mu}M C in 2.5 yr. DOC from the diatom blooms was more labile, but was also incompletely mineralized, with 25-35% remaining after 2.5 yr. Neither nutrients nor labile carbonmore » (dextrose) added at 1.5 yr significantly stimulated DOC mineralization. The experiments indicate that DOC produced in short-term blooms can be surprisingly resistant to microbial attack. 21 refs., 1 fig., 1 tab.« less

Retrogressive thaw slumps temper dissolved organic carbon delivery to streams of the Peel Plateau, NWT, Canada

NASA Astrophysics Data System (ADS)

Littlefair, Cara A.; Tank, Suzanne E.; Kokelj, Steven V.

2017-12-01

In Siberia and Alaska, permafrost thaw has been associated with significant increases in the delivery of dissolved organic carbon (DOC) to recipient stream ecosystems. Here, we examine the effect of retrogressive thaw slumps (RTSs) on DOC concentration and transport, using data from eight RTS features on the Peel Plateau, NWT, Canada. Like extensive regions of northwestern Canada, the Peel Plateau is comprised of thick, ice-rich tills that were deposited at the margins of the Laurentide Ice Sheet. RTS features are now widespread in this region, with headwall exposures up to 30 m high and total disturbed areas often exceeding 20 ha. We find that intensive slumping on the Peel Plateau is universally associated with decreasing DOC concentrations downstream of slumps, even though the composition of slump-derived dissolved organic matter (DOM; assessed using specific UV absorbance and slope ratios) is similar to permafrost-derived DOM from other regions. Comparisons of upstream and downstream DOC flux relative to fluxes of total suspended solids suggest that the substantial fine-grained sediments released by RTS features may sequester DOC. Runoff obtained directly from slump rill water, above entry into recipient streams, indicates that the deepest RTS features, which thaw the greatest extent of buried, Pleistocene-aged glacial tills, release low-concentration DOC when compared to paired upstream, undisturbed locations, while shallower features, with exposures that are more limited to a relict Holocene active layer, have within-slump DOC concentrations more similar to upstream sites. Finally, fine-scale work at a single RTS site indicates that temperature and precipitation serve as primary environmental controls on above-slump and below-slump DOC flux, but it also shows that the relationship between climatic parameters and DOC flux is complex for these dynamic thermokarst features. These results demonstrate that we should expect clear variation in thermokarst-associated DOC mobilization across Arctic regions. However, they also show that within-region variation in thermokarst intensity and landscape composition is critical for determining the biogeochemical response. Geological and climate legacy shape the physical and chemical composition of permafrost and thermokarst potential. As such, these factors must be considered in predictions of land-to-water carbon mobilization in a warming Arctic.

Experimental determinations of soil copper toxicity to lettuce (Lactuca sativa) growth in highly different copper spiked and aged soils.

PubMed

Christiansen, Karen S; Borggaard, Ole K; Holm, Peter E; Vijver, Martina G; Hauschild, Michael Z; Peijnenburg, Willie J G M

2015-04-01

Accurate knowledge about factors and conditions determining copper (Cu) toxicity in soil is needed for predicting plant growth in various Cu-contaminated soils. Therefore, effects of Cu on growth (biomass production) of lettuce (Lactuca sativa) were tested on seven selected, very different soils spiked with Cu and aged for 2 months at 35 °C. Cu toxicity was expressed as pEC50(Cu(2+)), i.e., the negative logarithm of the EC50(Cu(2+)) activity to plant growth. The determined pEC50(Cu(2+)) was significantly and positively correlated with both the analytically readily available soil pH and concentration of dissolved organic carbon [DOC] which together could explain 87% of the pEC50(Cu(2+)) variation according to the simple equation: pEC50(Cu(2+)) = 0.98 × pH + 345 × [DOC] - 0.27. Other soil characteristics, including the base cation concentrations (Na(+), K(+), Ca(2+), Mg(2+)), the cation exchange capacity at soil pH (ECEC), and at pH 7 (CEC7), soil organic carbon, clay content, and electric conductivity as well as the distribution coefficient (Kd) calculated as the ratio between total soil Cu and water-extractable Cu did not correlate significantly with pEC50(Cu(2+)). Consequently, Cu toxicity, expressed as the negative log of the Cu(2+) activity, to plant growth increases at increasing pH and DOC, which needs to be considered in future management of plant growth on Cu-contaminated soils. The developed regression equation allows identification of soil types in which the phytotoxicity potential of Cu is highest.

Using fluorescence spectroscopy to gain new insights into seasonal patterns of stream DOC concentrations in an alpine, headwater catchment underlain by discontinuous permafrost in Wolf Creek Research Basin, Yukon Territory, Canada

NASA Astrophysics Data System (ADS)

Shatilla, N. J.; Carey, S.; Tang, W.

2017-12-01

The Canadian subarctic is experiencing rapid climate warming resulting in decreased depth and duration of snowcover, decreased permafrost extent and time span of seasonal frozen ground resulting in increased active layer depth, and increased frequency and magnitude of rainfall events during the growing season. These changes challenge our conceptual models of permafrost hydrology as comparisons between recent and historical streamflow records show an emerging secondary post-freshet peak in flow in recent years along with enhanced winter flows. Long-term monitoring of Granger Creek (7.6km2), an alpine watershed underlain by discontinuous permafrost located within Wolf Creek Research Basin (176km2) in Yukon Territory, Canada provided a multi-decadal record of hydro-meteorological measurements. Granger Creek experienced warmer and wetter summers in 2015-6 compared to 2001-8, and an altered streamflow pattern with an earlier spring freshet and peak in dissolved organic carbon (DOC) concentrations. DOC concentrations post-freshet remained low at both the headwater and meso-catchment scale, which contradicts trends of increasing DOC concentrations observed in larger river systems. Hysteresis loops of sub-hourly measurements of streamflow, salinity and chromophoric dissolved organic matter (CDOM) were analyzed to provide new insights into how hydrological connectivity at the headwater scale affected the timing of solute release with supporting information from optical indices calculated from fluorescence spectroscopy. These indices provided a more nuanced view of catchment dynamics than the DOC concentrations. The composition and quality of DOM varied throughout the growing season with the delivery of older, terrestrially-derived material corresponding to high DOC concentrations at the onset of spring freshet when the catchment was initially being flushed. The origin and quality of stream DOM shifted throughout the rest of the season to newer, more easily mobilized DOM. Comparison of historical and current data show a shift from the freshet-driven primary flush of DOC from the system to an increasingly important mobilization of solutes at the end of the growing season that could begin impacting the quantity and quality of solutes exported in the subsequent spring.

Assessment of copper, cadmium and zinc remobilization in Mediterranean marine coastal sediments

NASA Astrophysics Data System (ADS)

Sakellari, Aikaterini; Plavšić, Marta; Karavoltsos, Sotiris; Dassenakis, Manos; Scoullos, Michael

2011-01-01

The remobilization of copper, cadmium and zinc in sediments of three selected coastal microenvironments of the Aegean Sea (Eastern Mediterranean) is assessed. Various analytical methods and techniques were employed providing concentrations, profiles and forms of metals and organic matter in sediments and pore waters. At Loutropyrgos, a non-industrial site located, however, within an intensively industrialized enclosed gulf, an intense resupply of zinc in pore water from sediment was recorded, correlating with the highest value of weakly bound fraction of zinc determined at this area. The comparatively high zinc concentrations measured in the pore waters (394 nM), exceed considerably those in the overlying seawater (12.5 nM determined by DGT; 13.5 nM total), resulting in the formation of a strong concentration gradient at the sediment-water interface. Potential zinc flux at the sediment-water interface at Loutropyrgos (based on 0.4 mm DGT profile) was calculated equal to 0.8 mmol.m -2.d -1. The half lives of trace metals at Loutropyrgos site, based on the aforementioned DGT profiles, amount to 0.1 y (Zn), 2.8 y (Cd), 4.5 y (Cu), 2.2 y (Mn) and 0.4 y (Fe) pointing out to the reactivity of these metals at the sediment-water interface. The concentration of dissolved organic carbon (DOC) in pore waters of the three selected sites (2.7-5.2 mg/L) was up to four times higher compared to that of the corresponding overlying seawater. Similarly, the concentrations of carbohydrates in pore waters (0.20-0.91 mg/L monosaccharides; 0.71-1.6 mg/L polysaccharides) are an order of magnitude higher than those of seawater, forming a concentration gradient at the sediment-water interface. Total carbohydrates contribute between 34 and 48% of the organic carbon of the pore waters, being significantly higher than those of seawater from the corresponding areas, which were in the range of 15-21%. The complexing capacity as for copper ions (CCu) determined in pore water ranges widely, from 0.03 μM at Kalamos to 3.76 μM at Molos, whereas the corresponding values for cadmium ions (CCd) were non detectable, except for Kalamos site, where the value for CCd was equal to 0.03 μM. A significant increase in the values of CCu, normalized as for DOC, was observed in pore waters in relation to those of overlying seawater. This indicates an 'enrichment' of pore waters in dissolved organic ligands for copper ions per unit of DOC. Up to 72% of DOC could be present as ligands capable to complex copper ions.

Spatial and temporal variability in the amount and source of dissolved organic carbon: Implications for ultraviolet exposure in amphibian habitats

USGS Publications Warehouse

Brooks, P.D.; O'Reilly, C. M.; Diamond, S.A.; Campbell, D.H.; Knapp, R.; Bradford, D.; Corn, P.S.; Hossack, B.; Tonnessen, K.

2005-01-01

The amount, chemical composition, and source of dissolved organic carbon (DOC), together with in situ ultraviolet (UV-B) attenuation, were measured at 1–2 week intervals throughout the summers of 1999, 2000, and 2001 at four sites in Rocky Mountain National Park (Colorado). Eight additional sites, four in Sequoia and Kings Canyon National Park/John Muir Wilderness (California) and four in Glacier National Park (Montana), were sampled during the summer of 2000. Attenuation of UV-B was significantly related to DOC concentrations over the three years in Rocky Mountain (R2 = 0.39, F = 25.71, P < 0.0001) and across all parks in 2000 (R2 = 0.44, F = 38.25, P < 0.0001). The relatively low R2 values, however, reflect significant temporal and spatial variability in the specific attenuation per unit DOC. Fluorescence analysis of the fulvic acid DOC fraction (roughly 600–2,000 Daltons) indicated that the source of DOC significantly affected the attenuation of UV-B. Sites in Sequoia–Kings Canyon were characterized by DOC derived primarily from algal sources and showed much deeper UV-B penetration, whereas sites in Glacier and Rocky Mountain contained a mix of algal and terrestrial DOC-dominated sites, with more terrestrially dominated sites characterized by greater UV-B attenuation per unit DOC. In general, site characteristics that promoted the accumulation of terrestrially derived DOC showed greater attenuation of UV-B per unit DOC; however, catchment vegetation and soil characteristics, precipitation, and local hydrology interacted to make it difficult to predict potential exposure from DOC concentrations.

Climate change and dissolved organic carbon export to the Gulf of Maine

USGS Publications Warehouse

Huntington, Thomas G.; Balch, William M.; Aiken, George R.; Sheffield, Justin; Luo, Lifeng; Roesler, Collin S.; Camill, Philip

2016-01-01

Ongoing climate change is affecting the concentration, export (flux), and timing of dissolved organic carbon (DOC) exported to the Gulf of Maine (GoM) through changes in hydrologic regime. DOC export was calculated for water years 1950 through 2013 for 20 rivers and for water years 1930 through 2013 for 14 rivers draining to the GoM. DOC export was also estimated for the 21st century based on climate and hydrologic modeling in a previously published study. DOC export was calculated by using the regression model LOADEST to fit seasonally adjusted concentration discharge (C-Q) relations. Our results are an analysis of the sensitivity of DOC export to changes in hydrologic conditions over time since land cover and vegetation were held constant over time. Despite large interannual variability, all rivers had increasing DOC export during winter and these trends were significant (p < 0.05) in 10 out of 20 rivers for 1950 to 2013 and in 13 out of 14 rivers for 1930 to 2013. All rivers also had increasing annual export of DOC although fewer trends were statistically significant than for winter export. Projections for DOC export during the 21st century were variable depending on the climate model and greenhouse gas emission scenario that affected future river discharge through effects on precipitation and evapotranspiration. The most consistent result was a significant increase in DOC export in winter in all model-by-emission scenarios. DOC export was projected to decrease during the summer in all model-by-emission scenarios, with statistically significant decreases in half of the scenarios.

Landscape scale controls on the vascular plant component of dissolved organic carbon across a freshwater delta

USGS Publications Warehouse

Eckard, Robert S.; Hernes, Peter J.; Bergamaschi, Brian A.; Stepanauskas, Ramunas; Kendall, Carol

2007-01-01

Lignin phenol concentrations and compositions were determined on dissolved organic carbon (DOC) extracts (XAD resins) within the Sacramento-San Joaquin River Delta (the Delta), the tidal freshwater portion of the San Francisco Bay Estuary, located in central California, USA. Fourteen stations were sampled, including the following habitats and land-use types: wetland, riverine, channelized waterway, open water, and island drains. Stations were sampled approximately seasonally from December, 1999 through May, 2001. DOC concentrations ranged from 1.3 mg L-1 within the Sacramento River to 39.9 mg L-1 at the outfall from an island drain (median 3.0 mg L-1), while lignin concentrations ranged from 3.0 μL-1 within the Sacramento River to 111 μL-1 at the outfall from an island drain (median 11.6 μL-1). Both DOC and lignin concentrations varied significantly among habitat/land-use types and among sampling stations. Carbon-normalized lignin yields ranged from 0.07 mg (100 mg OC)-1 at an island drain to 0.84 mg (100 mg OC)-1 for a wetland (median 0.36 mg (100 mg OC)-1), and also varied significantly among habitat/land-use types. A simple mass balance model indicated that the Delta acted as a source of lignin during late autumn through spring (10-83% increase) and a sink for lignin during summer and autumn (13-39% decrease). Endmember mixing models using S:V and C:V signatures of landscape scale features indicated strong temporal variation in sources of DOC export from the Delta, with riverine source signatures responsible for 50% of DOC in summer and winter, wetland signatures responsible for 40% of DOC in summer, winter, and late autumn, and island drains responsible for 40% of exported DOC in late autumn. A significant negative correlation was observed between carbon-normalized lignin yields and DOC bioavailability in two of the 14 sampling stations. This study is, to our knowledge, the first to describe organic vascular plant DOC sources at the level of localized landscape features, and is also the first to indicate a significant negative correlation between lignin and DOC bioavailability within environmental samples. Based upon observed trends: (1) Delta features exhibit significant spatial variability in organic chemical composition, and (2) localized Delta features appear to exert strong controls on terrigenous DOC as it passes through the Delta and is exported into the Pacific Ocean.

Effects of biodiesel, engine load and diesel particulate filter on nonvolatile particle number size distributions in heavy-duty diesel engine exhaust.

PubMed

Young, Li-Hao; Liou, Yi-Jyun; Cheng, Man-Ting; Lu, Jau-Huai; Yang, Hsi-Hsien; Tsai, Ying I; Wang, Lin-Chi; Chen, Chung-Bang; Lai, Jim-Shoung

2012-01-15

Diesel engine exhaust contains large numbers of submicrometer particles that degrade air quality and human health. This study examines the number emission characteristics of 10-1000 nm nonvolatile particles from a heavy-duty diesel engine, operating with various waste cooking oil biodiesel blends (B2, B10 and B20), engine loads (0%, 25%, 50% and 75%) and a diesel oxidation catalyst plus diesel particulate filter (DOC+DPF) under steady modes. For a given load, the total particle number concentrations (N(TOT)) decrease slightly, while the mode diameters show negligible changes with increasing biodiesel blends. For a given biodiesel blend, both the N(TOT) and mode diameters increase modestly with increasing load of above 25%. The N(TOT) at idle are highest and their size distributions are strongly affected by condensation and possible nucleation of semivolatile materials. Nonvolatile cores of diameters less than 16 nm are only observed at idle mode. The DOC+DPF shows remarkable filtration efficiency for both the core and soot particles, irrespective of the biodiesel blend and engine load under study. The N(TOT) post the DOC+DPF are comparable to typical ambient levels of ≈ 10(4)cm(-3). This implies that, without concurrent reductions of semivolatile materials, the formation of semivolatile nucleation mode particles post the after treatment is highly favored. Copyright © 2011 Elsevier B.V. All rights reserved.

Dissolved oxygen as an indicator of bioavailable dissolved organic carbon in groundwater.

PubMed

Chapelle, Francis H; Bradley, Paul M; McMahon, Peter B; Kaiser, Karl; Benner, Ron

2012-01-01

Concentrations of dissolved oxygen (DO) plotted vs. dissolved organic carbon (DOC) in groundwater samples taken from a coastal plain aquifer of South Carolina (SC) showed a statistically significant hyperbolic relationship. In contrast, DO-DOC plots of groundwater samples taken from the eastern San Joaquin Valley of California (CA) showed a random scatter. It was hypothesized that differences in the bioavailability of naturally occurring DOC might contribute to these observations. This hypothesis was examined by comparing nine different biochemical indicators of DOC bioavailability in groundwater sampled from these two systems. Concentrations of DOC, total hydrolysable neutral sugars (THNS), total hydrolysable amino acids (THAA), mole% glycine of THAA, initial bacterial cell counts, bacterial growth rates, and carbon dioxide production/consumption were greater in SC samples relative to CA samples. In contrast, the mole% glucose of THNS and the aromaticity (SUVA(254)) of DOC was greater in CA samples. Each of these indicator parameters were observed to change with depth in the SC system in a manner consistent with active biodegradation. These results are uniformly consistent with the hypothesis that the bioavailability of DOC is greater in SC relative to CA groundwater samples. This, in turn, suggests that the presence/absence of a hyperbolic DO-DOC relationship may be a qualitative indicator of relative DOC bioavailability in groundwater systems. Ground Water © 2011, National Ground Water Association. Published 2011. This article is a U.S. Government work and is in the public domain in the USA.

Improved automation of dissolved organic carbon sampling for organic-rich surface waters.

PubMed

Grayson, Richard P; Holden, Joseph

2016-02-01

In-situ UV-Vis spectrophotometers offer the potential for improved estimates of dissolved organic carbon (DOC) fluxes for organic-rich systems such as peatlands because they are able to sample and log DOC proxies automatically through time at low cost. In turn, this could enable improved total carbon budget estimates for peatlands. The ability of such instruments to accurately measure DOC depends on a number of factors, not least of which is how absorbance measurements relate to DOC and the environmental conditions. Here we test the ability of a S::can Spectro::lyser™ for measuring DOC in peatland streams with routinely high DOC concentrations. Through analysis of the spectral response data collected by the instrument we have been able to accurately measure DOC up to 66 mg L(-1), which is more than double the original upper calibration limit for this particular instrument. A linear regression modelling approach resulted in an accuracy >95%. The greatest accuracy was achieved when absorbance values for several different wavelengths were used at the same time in the model. However, an accuracy >90% was achieved using absorbance values for a single wavelength to predict DOC concentration. Our calculations indicated that, for organic-rich systems, in-situ measurement with a scanning spectrophotometer can improve fluvial DOC flux estimates by 6 to 8% compared with traditional sampling methods. Thus, our techniques pave the way for improved long-term carbon budget calculations from organic-rich systems such as peatlands. Copyright © 2015 Elsevier B.V. All rights reserved.

Overview of a simple model describing variation of dissolved organic carbon in an upland catchment

USGS Publications Warehouse

Boyer, Elizabeth W.; Hornberger, George M.; Bencala, Kenneth E.; McKnight, Diane M.

1996-01-01

Hydrological mechanisms controlling the variation of dissolved organic carbon (DOC) were investigated in the Deer Creek catchment located near Montezuma, CO. Patterns of DOC in streamflow suggested that increased flows through the upper soil horizon during snowmelt are responsible for flushing this DOC-enriched interstitial water to the streams. We examined possible hydrological mechanisms to explain the observed variability of DOC in Deer Creek by first simulating the hydrological response of the catchment using TOPMODEL and then routing the predicted flows through a simple model that accounted for temporal changes in DOC. Conceptually the DOC model can be taken to represent a terrestrial (soil) reservoir in which DOC builds up during low flow periods and is flushed out when infiltrating meltwaters cause the water table to rise into this “reservoir”. Concentrations of DOC measured in the upper soil and in streamflow were compared to model simulations. The simulated DOC response provides a reasonable reproduction of the observed dynamics of DOC in the stream at Deer Creek.

'invisible' DOM in hourly-resolved headwater river records from Northern Amazonia

NASA Astrophysics Data System (ADS)

Pereira, R.; Bovolo, C.; Spencer, R. G.; Hernes, P. J.; Tipping, E.; Vieth-Hillebrand, A.; Chappell, N.; Lewis-Franklin, A.; Parkin, G.; Wagner, T.

2012-12-01

Global river networks annually process ~3 billion tonnes of organic carbon but only ~17% reaches the ocean. These estimates suggest rivers are not mere transportation pipes but biogeochemical reactors. Inland waters are therefore fundamental to the understanding of carbon and nutrient interactions between land and ocean. Within these global estimates, tropical rivers contribute ~two-thirds of the global dissolved organic matter flux to the ocean. Recent studies suggest that up to 50% of the CO2 outgassed from tropical rivers is derived from terrestrial organic matter and that the terrestrial-aquatic interface in river headwaters are hotspots of biochemical activity. However, to date, most tropical riverine studies focus on the main river stem or mouth and therefore the dynamics of tropical headwater organic matter cycling within the global carbon cycle are unknown. We present a geochemical and hydrological time-series (sub-hourly resolution) of river water DOC concentration, source and composition from a pristine lowland rainforest headwater of the Burro Burro River, a tributary of the Essequibo River, the 3rd largest river in S. America. We show that during and after a rainstorm event, DOC concentrations increase an order of magnitude (10 to 114mg/L) in less than 30 mins, far exceeding the entire seasonal DOC range measured in 2010 and 2011 (17-28mg/L). The source (δ13C-DOC) of DOC during the rainstorm event changes from microbial/aquatic (-21.9‰ to -25.7‰) at low/intermediate DOC concentration to C3 vegetation supply (-26.8‰ to -30.3‰) during peak DOC flushing. First radiocarbon data shows that riverine DOC is relatively young (106.8-110.9 %modern), however, tropical soils suggest a potential for organic matter to be preserved (360-1200 BP). The fundamental relationship between DOC and coloured dissolved organic matter (CDOM), measured as UV absorbance (SUVA254), holds only for low riverine DOC concentrations with proportionally high lignin contribution, whereas high levels in DOC are not explained by humic substances. Size exclusion chromatography confirms that the DOM pool is divided into two main fractions, humic substances and 'invisible' DOM, or 'iDOM'. The latter group includes non UV-absorbing organic compounds of mono- and oligosaccharides, alcohols, aldehydes, ketones and amino sugars. Our new records from Guyana show that whilst lignin phenols are present and closely track the UV absorbance (R2 = 0.97), it is iDOM that dominates the total DOC pool at peak concentrations (up to 84%). Notably, iDOM is still found in the main Burro Burro River (20-40%), indicating that iDOM has some potential to survive transport downstream. The results suggest that DOC could be significantly underestimated in tropical systems due to the observed decoupling of DOC, water colour (CDOM) and river flux related to large amounts of iDOM entering the river during rainstorm events and wet seasons. Furthermore, given that headwaters represent roughly 50-85% of the total area of tropical river catchments, it is likely that iDOM is a significant component of the terrestrial carbon and nutrient cycles. It is therefore necessary to conduct further field studies that will produce high resolution (temporal and spatial) geochemical records from a large number of tropical systems to better quantify the role of tropical inland waters in carbon and nutrient cycling.

Linking major and trace element headwater stream concentrations to DOC release and hydrologic conditions in a bog and peaty riparian zone

NASA Astrophysics Data System (ADS)

Broder, Tanja; Biester, Harald

2017-04-01

Peatlands and organic-rich riparian zones are known to export large amounts of dissolved organic carbon (DOC) to surface water. In organic-rich, acidic headwater streams main carriers for element export are dissolved organic matter (DOM) and organic-iron complexes. In this environment DOM might also act as major carrier for metals, which otherwise may have a low solubility. This study examines annual and short term event-based variations of major and trace elements in a headwater catchment. Patterns are used to trace hydrological pathways and element sources under different hydrologic preconditions. Furthermore, it elucidates the importance of DOC as carrier of different elements in a bog and a peaty riparian catchment. The study was conducted in a small headwater stream draining an ombrotrophic peatland with an adjacent forested area with peaty riparian soils in the Harz Mountains (Germany). Discharge sampling was conducted weekly at two sites from snowmelt to begin of snowfall and in high resolution during selected discharge events in 2013 and 2014. Element concentrations were measured by means of ICP-MS and ICP-OES. A PCA was performed for each site and for annual and event datasets. Results show that a large number of element concentrations strongly correlate with DOC concentrations at the bog site. Even elements like Ca and Mg, which are known to have a low affinity to DOC. Congruently, the first principal component integrates the DOC pattern (element loadings > 0.8: Ca, Fe, Mg, Mn, Zn, As, Sr, Cd, DOC) and explained about 35 % of total variance and even 50 % during rain events (loadings > 0.8: Al, Ca, Fe, Mg, Mn, Zn, Li, Co, As, Sr, Cd, Pb, DOC). The study cannot verify that all correlating elements bind to DOC. It is likely that also a common mobilization pattern in the upper peat layer by plant decomposition causes the same response to changes in hydrologic pathways. Additionally, a low mineral content and an enrichment of elements like Fe and Mn in the upper peat layers due to prevailing redox conditions might play a major role in a bog environment. At the peaty riparian zone only Ca, Fe, and Sr strongly correlated with DOC over the annual record. The PCA of the annual record display no clear DOC component here, but indicates that DOC is influenced by Component one (element loadings > 0.8: Ca, Mg, Zn, Co, Sr) and two (Al, V, La, Pb, U) suggesting different DOC sources in the peaty riparian zone. A large number of elements correlate with DOC during rain event sampling at the riparian zone. In contrast to the bog site the event-based riparian zone PCA distinguished a clear discharge related component with mineral, groundwater related elements (K, Rb, In, Cs, NO3- and SO42-). Pattern of the mineral and DOC components prove that during base flow discharge is generated in a shallow groundwater layer and successively increases upward to the organic-rich upper soil layer with increasing discharge. Contrarily, bog element pattern confirm a dominating surface-near discharge, due to high hydraulic conductivities.

Rapid Response of Hydrological Loss of DOC to Water Table Drawdown and Warming in Zoige Peatland: Results from a Mesocosm Experiment

PubMed Central

Lou, Xue-Dong; Zhai, Sheng-Qiang; Kang, Bing; Hu, Ya-Lin; Hu, Li-Le

2014-01-01

A large portion of the global carbon pool is stored in peatlands, which are sensitive to a changing environment conditions. The hydrological loss of dissolved organic carbon (DOC) is believed to play a key role in determining the carbon balance in peatlands. Zoige peatland, the largest peat store in China, is experiencing climatic warming and drying as well as experiencing severe artificial drainage. Using a fully crossed factorial design, we experimentally manipulated temperature and controlled the water tables in large mesocosms containing intact peat monoliths. Specifically, we determined the impact of warming and water table position on the hydrological loss of DOC, the exported amounts, concentrations and qualities of DOC, and the discharge volume in Zoige peatland. Our results revealed that of the water table position had a greater impact on DOC export than the warming treatment, which showed no interactive effects with the water table treatment. Both DOC concentration and discharge volume were significantly increased when water table drawdown, while only the DOC concentration was significantly promoted by warming treatment. Annual DOC export was increased by 69% and 102% when the water table, controlled at 0 cm, was experimentally lowered by −10 cm and −20 cm. Increases in colored and aromatic constituents of DOC (measured by Abs254 nm, SUVA254 nm, Abs400 nm, and SUVA400 nm) were observed under the lower water tables and at the higher peat temperature. Our results provide an indication of the potential impacts of climatic change and anthropogenic drainage on the carbon cycle and/or water storage in a peatland and simultaneously imply the likelihood of potential damage to downstream ecosystems. Furthermore, our results highlight the need for local protection and sustainable development, as well as suggest that more research is required to better understand the impacts of climatic change and artificial disturbances on peatland degradation. PMID:25369065

Rapid response of hydrological loss of DOC to water table drawdown and warming in Zoige peatland: results from a mesocosm experiment.

PubMed

Lou, Xue-Dong; Zhai, Sheng-Qiang; Kang, Bing; Hu, Ya-Lin; Hu, Li-Le

2014-01-01

A large portion of the global carbon pool is stored in peatlands, which are sensitive to a changing environment conditions. The hydrological loss of dissolved organic carbon (DOC) is believed to play a key role in determining the carbon balance in peatlands. Zoige peatland, the largest peat store in China, is experiencing climatic warming and drying as well as experiencing severe artificial drainage. Using a fully crossed factorial design, we experimentally manipulated temperature and controlled the water tables in large mesocosms containing intact peat monoliths. Specifically, we determined the impact of warming and water table position on the hydrological loss of DOC, the exported amounts, concentrations and qualities of DOC, and the discharge volume in Zoige peatland. Our results revealed that of the water table position had a greater impact on DOC export than the warming treatment, which showed no interactive effects with the water table treatment. Both DOC concentration and discharge volume were significantly increased when water table drawdown, while only the DOC concentration was significantly promoted by warming treatment. Annual DOC export was increased by 69% and 102% when the water table, controlled at 0 cm, was experimentally lowered by -10 cm and -20 cm. Increases in colored and aromatic constituents of DOC (measured by Abs(254 nm), SUVA(254 nm), Abs(400 nm), and SUVA(400 nm)) were observed under the lower water tables and at the higher peat temperature. Our results provide an indication of the potential impacts of climatic change and anthropogenic drainage on the carbon cycle and/or water storage in a peatland and simultaneously imply the likelihood of potential damage to downstream ecosystems. Furthermore, our results highlight the need for local protection and sustainable development, as well as suggest that more research is required to better understand the impacts of climatic change and artificial disturbances on peatland degradation.

Atmospheric inputs of organic matter to a forested watershed: Variations from storm to storm over the seasons

USGS Publications Warehouse

Iavorivska , Lidiia; Boyer, Elizabeth W.; Miller, Matthew P.; Brown, Michael G.; Vasilopoulos , Terrie; Fuentes, Jose D.; Duffy, Christopher J.

2016-01-01

The objectives of this study were to determine the quantity and chemical composition of precipitation inputs of dissolved organic carbon (DOC) to a forested watershed; and to characterize the associated temporal variability. We sampled most precipitation that occurred from May 2012 through August 2013 at the Susquehanna Shale Hills Critical Zone Observatory (Pennsylvania, USA). Sub-event precipitation samples (159) were collected sequentially during 90 events; covering various types of synoptic meteorological conditions in all climatic seasons. Precipitation DOC concentrations and rates of wet atmospheric DOC deposition were highly variable from storm to storm, ranging from 0.3 to 5.6 mg C L−1 and from 0.5 to 32.8 mg C m−2 h−1, respectively. Seasonally, storms in spring and summer had higher concentrations of DOC and more optically active organic matter than in winter. Higher DOC concentrations resulted from weather types that favor air advection, where cold frontal systems, on average, delivered more than warm/stationary fronts and northeasters. A mixed modeling statistical approach revealed that factors related to storm properties, emission sources, and to the chemical composition of the atmosphere could explain more than 60% of the storm to storm variability in DOC concentrations. This study provided observations on changes in dissolved organic matter that can be useful in modeling of atmospheric oxidative chemistry, exploring relationships between organics and other elements of precipitation chemistry, and in considering temporal changes in ecosystem nutrient balances and microbial activity.

Lake transparency: a window into decadal variations in dissolved organic carbon concentrations in Lakes of Acadia National Park, Maine

USGS Publications Warehouse

Roesler, Collin S.; Culbertson, Charles W.

2016-01-01

A forty year time series of Secchi depth observations from approximately 25 lakes in Acadia National Park, Maine, USA, evidences large variations in transparency between lakes but relatively little seasonal cycle within lakes. However, there are coherent patterns over the time series, suggesting large scale processes are responsible. It has been suggested that variations in colored dissolved organic matter (CDOM) are primarily responsible for the variations in transparency, both between lakes and over time and further that CDOM is a robust optical proxy for dissolved organic carbon (DOC). Here we present a forward model of Secchi depth as a function of DOC based upon first principles and bio-optical relationships. Inverting the model to estimate DOC concentration from Secchi depth observations compared well with the measured DOC concentrations collected since 1995 (RMS error < 1.3 mg C l-1). This inverse model allows the time series of DOC to be extended back to the mid 1970s when only Secchi depth observations were collected, and thus provides a means for investigating lake response to climate forcing, changing atmospheric chemistry and watershed characteristics, including land cover and land use.

Dissolved Organic Carbon Mobilisation in a Groundwater System Stressed by Pumping

PubMed Central

Graham, P. W.; Baker, A.; Andersen, M. S.

2015-01-01

The concentration and flux of organic carbon in aquifers is influenced by recharge and abstraction, and surface and subsurface processing. In this study groundwater was abstracted from a shallow fractured rock aquifer and dissolved organic carbon (DOC) was measured in observation bores at different distances from the abstraction bore. Groundwater abstraction at rates exceeding the aquifers yield resulted in increased DOC concentration up to 3,500 percent of initial concentrations. Potential sources of this increased DOC were determined using optical fluorescence and absorbance analysis. Groundwater fluorescent dissolved organic material (FDOM) were found to be a combination of terrestrial-derived humic material and microbial or protein sourced material. Relative molecular weight of FDOM within four metres of the abstraction well increased during the experiment, while the relative molecular weight of FDOM between four and ten metres from the abstraction well decreased. When the aquifer is not being pumped, DOC mobilisation in the aquifer is low. We hypothesise that the physical shear stress on aquifer materials caused by intense abstraction significantly increases the temporary release of DOC from sloughing of biofilms and release of otherwise bound colloidal and sedimentary organic carbon (SOC). PMID:26691238

How appetizing is the dissolved organic matter (DOM) trees lose during rainfall?

NASA Astrophysics Data System (ADS)

Howard, D.; Van Stan, J. T., II; Whitetree, A.; Zhu, L.; Stubbins, A.

2017-12-01

Dissolved organic carbon (DOC) is the chemical backbone of dissolved organic matter (DOM), which is important because it drives many processes in soils and waterways. Current DOC work has paid little attention to interactions between rain and plant canopies, where rainfall is partitioned into throughfall and stemflow. Even less DOC research has investigated the effect of arboreal epiphytes on throughfall and stemflow DOC. The purpose of this study is twofold: (1) assess the degree and timing of DOC consumption by microbial communities (biolability) in throughfall and stemflow, and (2) determine whether the presence of arboreal epiphytes in the canopy affect DOC biolability. Biolability of stemflow and throughfall DOC from Juniperus virginiana (cedar) was determined by incubating samples for 14 days. Throughfall and stemflow DOC was highly biolabile with DOC concentrations decreasing by 30-60%. Throughfall DOC was more biolabile than stemflow DOC. DOC in both throughfall and stemflow from epiphyte-covered cedars was less biolabile than DOC from trees without epiphytes. The high biolability of tree-derived DOC indicates that its supply provides carbon substrates to the microbial community at the forest floor, in soils and the rhizosphere. Epiphytes appear to be important in determining the biolability of DOC and therefore the size of this carbon subsidy to the soil ecosystem.

Seasonal variations of dissolved organic carbon in precipitation over urban and forest sites in central Poland.

PubMed

Siudek, Patrycja; Frankowski, Marcin; Siepak, Jerzy

2015-07-01

Spatial and temporal variability of carbon species in rainwater (bulk deposition) was studied for the first time at two sites located in urban area of Poznań City and protected woodland area (Jeziory), in central Poland, between April and December 2013. The mean concentration of total carbon (TC) for the first site was 5.86 mg L(-1), whereas for the second, 5.21 mg L(-1). Dissolved organic carbon (DOC) concentration accounted for, on average, 87 and 91 % of total carbon in precipitation at urban and non-urban sites, respectively. Significant changes in TC concentrations in rainwater were observed at both sites, indicating that atmospheric transformation, transport, and removal mechanisms of carbonaceous particles were affected by seasonal fluctuations in biogenic/anthropogenic emission and meteorological conditions (i.e., precipitation height and type, atmospheric transport). During the warm season, the DOC concentration in rainwater was mostly influenced by mixed natural and anthropogenic sources. In contrast, during the cold season, the DOC concentration significantly increased mainly as a result of anthropogenic activities, i.e., intensive coal combustion, domestic wood burning, high-temperature processes, etc. In addition, during the winter measurements, significant differences in mean DOC concentration (Kruskal-Wallis test, p < 0.05) were determined for rain, mixed rain-snow, and snow samples. It was found that rainwater TOC concentration measured in Poznań and Jeziory reflected a combination of local, regional, and distant sources. Backward trajectory analysis showed that air masses advected from polluted regions in western Europe largely affect the DOC amount in rainwater, both at urban and non-urban sites. These data imply that carbonaceous compounds are of crucial importance in atmospheric chemistry and should be considered as an important parameter while considering wet deposition, reactions with different substances, especially over polluted environments.

Dissolved Black Carbon in the Headwaters-To Continuum of PARAÍBA do Sul River, Brazil

NASA Astrophysics Data System (ADS)

Marques, Jomar S. J.; Dittmar, Thorsten; Niggemann, Jutta; Almeida, Marcelo G.; Gomez-Saez, Gonzalo V.; Rezende, Carlos E.

2017-02-01

Rivers annually carry 25-28 Tg carbon in the form of pyrogenic dissolved organic matter (dissolved black carbon, DBC) into the ocean, which is equivalent to about 10% of the entire riverine land-ocean flux of dissolved organic carbon (DOC). The objective of this study was to identify the main processes behind the release and turnover of DBC on a riverine catchment scale. As a model system, we chose the headwater-to-ocean continuum of Paraíba do Sul River (Brazil), the only river system with long-term DBC flux data available. The catchment was originally covered by Atlantic rain forest (mainly C3 plants) which was almost completely destroyed over the past centuries by slash-and-burn. As a result, large amounts of wood-derived charcoal reside in the soils. Today, fire-managed pasture and sugar cane (both dominated by C4 plants) cover most of the catchment area. Water samples were collected along the river, at the main tributaries, and also along the salinity gradient in the estuary and up to 35 km offshore during three different seasons. DBC was determined on a molecular level as benzenepolycarboxylic acids (BPCAs). Stable carbon isotopes (δ13C) were determined in solid phase extractable DOC (SPE-DOC) to distinguish C4 and C3 sources. Our results clearly show a relationship between hydrology and DBC concentrations in the river, with highest DBC concentrations and fluxes in the wet season (flux of 770 moles .sec 1 in 2013 and 59 moles .sec 1 in 2014) and lowest in the dry season (flux of 27 moles .sec 1). This relationship indicates that DBC is mainly mobilized from the upper soil horizons during heavy rainfalls. The relationship between DBC concentrations and δ13C-SPE-DOC indicated that most of DBC in the river system originated from C3 plants, i.e. from the historic burning event of the Atlantic rain forest. A conservative mixing model could largely reproduce the observed DBC fluxes within the catchment and the land to ocean continuum. Comparably slight deviations from conservative mixing were accompanied by changes in the molecular composition of DBC (i.e. the ratio of benzenepenta- to benzenehexacarboxylic acid) that are indicative for photodegradation of DBC.

Organic matter compositions of rivers draining into Hudson Bay: Present-day trends and potential as recorders of future climate change

NASA Astrophysics Data System (ADS)

Godin, Pamela; Macdonald, Robie W.; Kuzyk, Zou Zou A.; Goñi, Miguel A.; Stern, Gary A.

2017-07-01

Concentrations and compositions of particulate and dissolved organic carbon (POC and DOC, respectively) and aromatic compounds including lignin were analyzed in water samples from 17 rivers flowing into Hudson Bay, northern Canada. These rivers incorporate basins to the south with no permafrost to basins in the north with continuous permafrost, and dominant vegetation systems that include Boreal Forest, the Hudson Plains, Taiga Shield, and Tundra. Major latitudinal trends in organic carbon and lignin concentrations and compositions were evident, with both DOC and dissolved lignin concentrations dominating over their particulate counterparts and exhibiting significant correlations with total dissolved and suspended solids, respectively. The composition of lignin reaction products in terms of the syringyl, cinnamyl, and vanillyl compositions indicate mixed sources of vascular land plant-derived organic carbon, with woody gymnosperms contributions dominating in the southern river basins whereas nonwoody angiosperm sources were more important in the most northerly rivers. The composition of nonlignin aromatic compounds, which provides a tracer for nonvascular plant contributions, suggests stronger contributions from Sphagnum mosses to dissolved organic matter in rivers below the tree line, including those with large peat bogs in their basins. Acid/aldehyde ratios of the lignin products together with Δ14C data for DOC in selected rivers indicate that DOC has generally undergone greater alteration than POC. Interestingly, several northern rivers exhibited relatively old DOC according to the Δ14C data suggesting that either old DOC is being released from permafrost or old DOC survives river transport in these rivers.

Light climate and dissolved organic carbon concentration influence species-specific changes in fish zooplanktivory

USGS Publications Warehouse

Weidel, Brian C.; Baglini, Katherine; Jones, Stuart E.; Kelly, Patrick T.; Solomon, Christopher T.; Zwart, Jacob A.

2017-01-01

Dissolved organic carbon (DOC) in lakes reduces light penetration and limits fish production in low nutrient lakes, reportedly via reduced primary and secondary production. Alternatively, DOC and light reductions could influence fish by altering their visual feeding. Previous studies report mixed effects of DOC on feeding rates of zooplanktivorous fish, but most investigators tested effects of a single concentration of DOC against clear-water, turbid, or algal treatments. We used a controlled laboratory study to quantify the effects of a DOC gradient (3–19 mg L−1) on average light climate and the zooplankton feeding rate of 3 common, north temperate fishes. Light availability, which was inversely related to DOC concentration, had a positive and linear effect on zooplankton consumption by juvenile largemouth bass (Micropterus salmoides) and bluegill (Lepomis macrochirus), explaining 22% and 28% of the variation in consumption, respectively. By contrast, zooplankton feeding rates by fathead minnow (Pimephales promelas) were best predicted by a nonlinear, negative influence of light (R2 = 0.13). In bluegill feeding trials we found a general trend for positive selection of larger zooplankton (Cladocera and Chaoboridae); however, the light climate did not influence the selection of prey type. Largemouth bass selected for larger-bodied zooplankton, with weak evidence that selectivity for large Cladocera changed from negative to neutral selection based on electivity values across the light gradient. Our results suggest that the effect of DOC on the light climate of lakes may directly influence fish zooplanktivory and that this influence may vary among fish species.

Modelling hydrological processes and dissolved organic carbon dynamics in a rehabilitated Sphagnum-dominated peatland

NASA Astrophysics Data System (ADS)

Bernard-Jannin, Léonard; Binet, Stéphane; Gogo, Sébastien; Leroy, Fabien; Perdereau, Laurent; Laggoun-Défarge, Fatima

2017-04-01

Sphagnum-dominated peatlands represent a global major stock of carbon (C). Dissolved organic carbon (DOC) exports through runoff and leaching could reduce their potential C sink function and impact downstream water quality. DOC production in peatlands is strongly controlled by the hydrology, especially water table depth (WTD). Therefore, disturbances such as drainage can lead to increase DOC exports by lowering the WTD. Hydrological restoration (e.g. rewetting) can be undertaken to restore peatland functioning with an impact on DOC exports. The objective of this study is to assess the impact of drainage and rewetting on hydrological processes and their interactions with DOC dynamics in a Sphagnum dominated peatland. A hydrological model has been applied to a drained peatland (La Guette, France) which experienced a rewetting action on February 2014 and where WTD has been recorded in four piezometers at a 15 min time step since 2009. In addition, DOC concentrations in the peatland have been measured 6 times a year since 2014. The hydrological model is a WTD dependent reservoir model composed by two reservoirs representing the micro and macro porosity of the peatland (Binet et al., 2013). A DOC production module in both reservoirs was implemented based on temperature and WTD. The model was calibrated against WTD and DOC concentrations for each piezometer. The results show that the WTD in the study area is strongly affected by local meteorological conditions that could hide the effect of the rewetting action. The preliminary results evidenced that an additional source of water, identified as groundwater supply originating from the surrounding sandy layer aquifer, is necessary to maintain the water balance, especially during wet years (NS>0.8). Finally, the DOC module was able to describe DOC concentrations measured in the peatland and could be used to assess the impact of rewetting on DOC dynamics at different locations and to identify the factors of control of DOC exports at the peatland scale before and after the restoration. This simple conceptual model requires few data to operate. Its application on different sites with contrasted settings (hydrological and climatic conditions) could provide insight on the dominant hydrological processes and their impact on DOC dynamics in peatlands. Binet S., Gogo S., Laggoun-Défarge F., A water-table dependent reservoir model to investigate the effect of drought and vascular plant invasion on peatland hydrology, Journal of Hydrology, Volume 499, 30 August 2013, Pages 132-139, ISSN 0022-1694, http://dx.doi.org/10.1016/j.jhydrol.2013.06.035.

Efficient removal of recalcitrant deep-ocean dissolved organic matter during hydrothermal circulation

NASA Astrophysics Data System (ADS)

Hawkes, Jeffrey A.; Rossel, Pamela E.; Stubbins, Aron; Butterfield, David; Connelly, Douglas P.; Achterberg, Eric P.; Koschinsky, Andrea; Chavagnac, Valérie; Hansen, Christian T.; Bach, Wolfgang; Dittmar, Thorsten

2015-11-01

Oceanic dissolved organic carbon (DOC) is an important carbon pool, similar in magnitude to atmospheric CO2, but the fate of its oldest forms is not well understood. Hot hydrothermal circulation may facilitate the degradation of otherwise un-reactive dissolved organic matter, playing an important role in the long-term global carbon cycle. The oldest, most recalcitrant forms of DOC, which make up most of oceanic DOC, can be recovered by solid-phase extraction. Here we present measurements of solid-phase extractable DOC from samples collected between 2009 and 2013 at seven vent sites in the Atlantic, Pacific and Southern oceans, along with magnesium concentrations, a conservative tracer of water circulation through hydrothermal systems. We find that magnesium and solid-phase extractable DOC concentrations are correlated, suggesting that solid-phase extractable DOC is almost entirely lost from solution through mineralization or deposition during circulation through hydrothermal vents with fluid temperatures of 212-401 °C. In laboratory experiments, where we heated samples to 380 °C for four days, we found a similar removal efficiency. We conclude that thermal degradation alone can account for the loss of solid-phase extractable DOC in natural hydrothermal systems, and that its maximum lifetime is constrained by the timescale of hydrothermal cycling, at about 40 million years.

Characterization of CDOM absorption of reservoirs with its linkage of regions and ages across China.

PubMed

Shang, Yingxin; Song, Kaishan; Wen, Zhidan; Lyu, Lili; Zhao, Ying; Fang, Chong; Zhang, Bai

2018-03-28

The absorption of chromophoric dissolved organic matter (CDOM) is an important part of light absorptions in aquatic systems. The increasing eutrophication of reservoirs and regional characteristics would affect the CDOM properties sensitively which would be important for the application of remote sensing monitoring. The highest (4.07 ± 2.31 m -1 ) and lowest (0.79 ± 0.67 m -1 ) CDOM concentrations of reservoirs were observed in the northeastern lake region (NER) and Tibetan Plateau lake region (TPR), respectively. The differences between S 275-295 among the five lake regions were significant (p < 0.05) in which the steepest S 275-295 (0.0173 ± 0.0026 nm -1 ) was observed in TPR and the shallowest (0.0326 ± 0.0152 nm -1 ) in Yungui Plateau lake region (YGR). The strong relationships between a CDOM (355) and DOC appeared in the NER (R 2  = 0.43), eastern lake region (EAR) (R 2  = 0.69), Mengxin lake region (MXR) (R 2  = 0.61), and YGR (R 2  = 0.79) which would be a good proxy for DOC in regional reservoirs. Most of all, the correlation between reservoir's establishing time and CDOM absorption under oligotrophic states was relatively strong in the EAR and MXR regions. It indicated that the establishing time of reservoirs affected the CDOM absorption to some extent under the oligotrophic states without much human disturbance. Our results indicate CDOM absorption varies with regions, and the relationships between CDOM and DOC are variable for different regions. Therefore, DOC estimation in reservoirs through CDOM absorption needs to be considered according to lake regions and trophic states.

Role of dissolved organic carbon upon re-entrainment and surface properties of aquifer bacteria and bacteria-sized microspheres during subsurface transport (Invited)

NASA Astrophysics Data System (ADS)

Harvey, R. W.; Metge, D. W.; Mohanram, A.; Gao, X.; Chorover, J.

2010-12-01

Susceptibilities for in-situ re-entrainment of attached 0.2 and 1.0 μm (diameter) microspheres and groundwater bacteria (Pseudomonas stuzeri and uncultured, native bacteria) were assessed during transport studies involving an organically contaminated, sandy aquifer in Cape Cod, MA. Aquifer sediments between pairs of injection and sampling wells were initially loaded with fluorescently labeled, carboxylated microspheres and bacteria that had been stained with the DNA-specific fluorochrome 4',6-diamidino-2-phenylindole. In response to subsequent hydrodynamic perturbations and injections of deionized water (ionic strength reduction), anionic surfactants (77 μM linear alkylbenzene sulfonates, LAS) and non-ionic surfactant (76 μM polyoxyethylene sorbitan monooleate, Tween 80), differing patterns of re-entrainment were evident for the two colloids. Injections of anionic surfactant and deionized water were the most efficient in causing detachment of the highly hydrophilic and negatively charged microspheres, but largely ineffective in causing re-entrainment of bacteria. In contrast, the nonionic surfactant was highly effective in re-entraining bacteria, but not microspheres. The hydrophobicities and zeta potentials of the indigenous bacteria were highly sensitive to modest concentration changes (0.6 to 1.3 mg L-1) in groundwater dissolved organic carbon (DOC), whereas the microspheres were largely unaffected. The most hydrophilic and negatively charged bacterial community was isolated from groundwater having the lowest DOC. FTIR spectra indicated that the community from the lowest DOC groundwater also had the highest average density of surface carboxyl groups. This indicates that DOC may have a biological effect on native bacteria resulting in changes to surface structures or changes in the makeup of the bacterial community.

The Relationship Between DOC Partition Coefficient and Mineral Soil C:N Ratio

NASA Astrophysics Data System (ADS)

Aitkenhead-Peterson, J. A.; McDowell, W. H.

2001-12-01

Since our recent publication showing that soil C:N predicts DOC flux at local and global scales, an effort has been made to understand mechanisms controlling the relationship between the two variables. We have approached this at multiple scales, using soil batch experiments, soil column experiments, and long-term field manipulations. We present here the results from our batch adsorption experiment. Mineral soils from tropical (wet and moist) and temperate (coniferous and hardwood) forests were used to assess DOC adsorption by the initial mass isotherm approach. We found that the DOC partition co-efficient (m) which represents a soil's tendency to adsorb DOC is strongly and inversely related to mineral soil C:N ratio (R2 = 0.99 n = 10 p < 0.001). The intercept of the mass isotherm, or the desorption term, was positively related to mineral soil C:N ratio (R2 = 0.80 n = 10 p < 0.01), but we found that desorption of DOC was more closely correlated with equilibrium DOC concentration (R2 = 0.97 n = 10 p < 0.001) than with mineral soil C:N. The mass isotherm approach is also useful in calculating the reactive soil pool (RSP), the fraction of the soil pool of organic carbon that may be lost to leaching. The RSP was not significantly related to mineral soil C:N, but tropical soils tended to have a larger RSP than temperate soils. Although some of the tropical soils came from areas where the natural forest had been cleared, used for plantations and then abandoned, the relationship between DOC adsorption and mineral soil C:N was not compromised. Watershed soil C:N ratio is an excellent predictor of DOC export because soil C:N is related to physiochemical adsorption processes in mineral soils and biotic production of DOC in organic soil horizons. It appears that soil C:N is a relatively robust predictor of soil solution DOC concentration and surface water DOC export for ecosystems undergoing environmental stress.

Modelling impacts of temperature, and acidifying and eutrophying deposition on DOC trends

NASA Astrophysics Data System (ADS)

Sawicka, Kasia; Rowe, Ed; Evans, Chris; Monteith, Don; Vanguelova, Elena; Wade, Andrew; Clark, Joanna

2017-04-01

Surface water dissolved organic carbon (DOC) concentrations in large parts of the northern hemisphere have risen over the past three decades, raising concern about enhanced contributions of carbon to the atmosphere and seas and oceans. The effect of declining acid deposition has been identified as a key control on DOC trends in soil and surface waters, since pH and ionic strength affect sorption and desorption of DOC. However, since DOC is derived mainly from recently-fixed carbon, and organic matter decomposition rates are considered sensitive to temperature, uncertainty persists regarding the extent to the relative importance of different drivers that affect these upward trends. We ran the dynamic model MADOC (Model of Acidity and Soil Organic Carbon) for a range of UK soils (podzols, gleysols and peatland), for which the time-series were available, to consider the likely relative importance of decreased deposition of sulphate and chloride, accumulation of reactive N, and higher temperatures, on DOC production in different soils. Modelled patterns of DOC change generally agreed favourably with measurements collated over 10-20 years, but differed markedly between sites. While the acidifying effect of sulphur deposition appeared to be the predominant control on the observed soil water DOC trends in all the soils considered other than a blanket peat, the model suggested that over the long term, the effects of nitrogen deposition on N-limited soils may have been sufficient to elevate the DOC recovery trajectory significantly. The second most influential cause of rising DOC in the model simulations was N deposition in ecosystems that are N-limited and respond with stimulated plant growth. Although non-marine chloride deposition made some contribution to acidification and recovery, it was not amongst the main drivers of DOC change. Warming had almost no effect on modelled historic DOC trends, but may prove to be a significant driver of DOC in future via its influence on nutrient availability and productivity. This suggests that current and future DOC concentrations could also exceed preindustrial levels due to the increased productivity of N enriched ecosystems, having important implications for drinking water catchment management and the setting and pursuit of appropriate restoration targets.

Molecular insights into the microbial formation of marine dissolved organic matter: recalcitrant or labile?

NASA Astrophysics Data System (ADS)

Koch, B. P.; Kattner, G.; Witt, M.; Passow, U.

2014-08-01

The degradation of marine dissolved organic matter (DOM) is an important control variable in the global carbon cycle. For our understanding of the kinetics of organic matter cycling in the ocean, it is crucial to achieve a mechanistic and molecular understanding of its transformation processes. A long-term microbial experiment was performed to follow the production of non-labile DOM by marine bacteria. Two different glucose concentrations and dissolved algal exudates were used as substrates. We monitored the bacterial abundance, concentrations of dissolved and particulate organic carbon (DOC, POC), nutrients, amino acids and transparent exopolymer particles (TEP) for 2 years. The molecular characterization of extracted DOM was performed by ultrahigh resolution Fourier transform ion cyclotron resonance mass spectrometry (FT-ICR MS) after 70 days and after ∼2 years of incubation. Although glucose quickly degraded, a non-labile DOC background (5-9% of the initial DOC) was generated in the glucose incubations. Only 20% of the organic carbon from the algal exudate degraded within the 2 years of incubation. The degradation rates for the non-labile DOC background in the different treatments varied between 1 and 11 μmol DOC L-1 year-1. Transparent exopolymer particles, which are released by microorganisms, were produced during glucose degradation but decreased back to half of the maximum concentration within less than 3 weeks (degradation rate: 25 μg xanthan gum equivalents L-1 d-1) and were below detection in all treatments after 2 years. Additional glucose was added after 2 years to test whether labile substrate can promote the degradation of background DOC (co-metabolism; priming effect). A priming effect was not observed but the glucose addition led to a slight increase of background DOC. The molecular analysis demonstrated that DOM generated during glucose degradation differed appreciably from DOM transformed during the degradation of the algal exudates. Our results led to several conclusions: (i) based on our experimental setup, higher substrate concentration resulted in a higher concentration of non-labile DOC; (ii) TEP, generated by bacteria, degrade rapidly, thus limiting their potential contribution to carbon sequestration; (iii) the molecular signatures of DOM derived from algal exudates and glucose after 70 days of incubation differed strongly from refractory DOM. After 2 years, however, the molecular patterns of DOM in glucose incubations were more similar to deep ocean DOM whereas the degraded exudate was still different.

Abundance, stable isotopic composition, and export fluxes of DOC, POC, and DIC from the Lower Mississippi River during 2006–2008

USGS Publications Warehouse

Cai, Yihua; Guo, Laodong; Wang, Xuri; Aiken, George R.

2015-01-01

Sources, abundance, isotopic compositions, and export fluxes of dissolved inorganic carbon (DIC), dissolved and colloidal organic carbon (DOC and COC), and particulate organic carbon (POC), and their response to hydrologic regimes were examined through monthly sampling from the Lower Mississippi River during 2006–2008. DIC was the most abundant carbon species, followed by POC and DOC. Concentration and δ13C of DIC decreased with increasing river discharge, while those of DOC remained fairly stable. COC comprised 61 ± 3% of the bulk DOC with similar δ13C abundances but higher percentages of hydrophobic organic acids than DOC, suggesting its aromatic and diagenetically younger status. POC showed peak concentrations during medium flooding events and at the rising limb of large flooding events. While δ13C-POC increased, δ15N of particulate nitrogen decreased with increasing discharge. Overall, the differences in δ13C between DOC or DIC and POC show an inverse correlation with river discharge. The higher input of soil organic matter and respired CO2 during wet seasons was likely the main driver for the convergence of δ13C between DIC and DOC or POC, whereas enhanced in situ primary production and respiration during dry seasons might be responsible for their isotopic divergence. Carbon export fluxes from the Mississippi River were estimated to be 13.6 Tg C yr−1 for DIC, 1.88 Tg C yr−1 for DOC, and 2.30 Tg C yr−1 for POC during 2006–2008. The discharge-normalized DIC yield decreased during wet seasons, while those of POC and DOC increased and remained constant, respectively, implying variable responses in carbon export to the increasing discharge.

The role of wildfires and forest succession in stream biogeochemistry within the continuous permafrost zone of Central Siberia

NASA Astrophysics Data System (ADS)

Prokushkin, Anatoly

2016-04-01

Wildfires transform boreal and subarctic forested landscapes leading to the changes in organic matter and inorganic nutrient turnover in terrestrial ecosystems. To get an insight to the fire effect on C fluxes and general hydrochemical characteristics of streams draining continuous permafrost terrains of Central Siberian Plateau (64o N 100o E), we have selected the chronosequence of basins (n = 17) which were severely affected by fires (>80% of basin area) in the time range from 1 to 116 years ago. Stream waters were sampled continuously during frost free seasons (May-September) of 2006-2015. Four streams have been equipped with water level, temperature and conductivity probes for continuous monitoring. The strongest negative effect of wildfires on dissolved organic carbon (DOC) concentrations in streams has occurred right after a fire event, and minimum mean annual concentrations of DOC appeared between 15 and 20 years elapsed after a fire. The most pronounced decrease in DOC concentrations during an annual cycle found in freshet period (May-June) and summer-fall storm events: differences of DOC concentrations among "intact" (>100 years after fire) and recent fire basins (<6 years) reached as much as 2-fold. Less differentiation among basins appears under lowflow conditions, as DOC-depleted solutes from deeper soil layers become dominating in stream flow. Following the post-fire forest recovery, the seasonal mean DOC concentrations in streams demonstrated linear growth at the rate of ca. 0.11 mgC/l/a and approached the initial values already after ca. 60 years after fire disturbance. An opposite trend (i.e. increasing load to streams after fire impact) was observed for dissolved inorganic carbon, major anions and cations. Sulfate was found to be a good tracer of fire affect as increased 200-fold in stream waters right after a fire and steady decreased at the rate [SO42-] = 3.65 x (year after fire)^-0.75 as terrestrial ecosystems were recovering after a fire. For study area, Na+ and Cl- in streams appear to be good indicators of permafrost degradation as they reflect talik formation and connection of a stream to underlying evaporitic deposits. While evidence of permafrost degradation is currently not apparent in the region, we expect increasing concentrations of Na+ and Cl- in streams of Central Siberian Plateau as permafrost degrades due to decreased fire return interval and warming temperatures. The generalized data of active layer thickness (ALT) within analyzed watersheds have demonstrated that fire-driven deepening of ALT results in increasing stream inorganic compounds concentrations. The inverse relationship found between DOC and ALT might be attributed to deeper infiltration of solutions, sorption of DOC on clay minerals, and an increasing rate of DOC microbiological mineralization to CO2 due to increased soil temperatures. Post-fire forest recovery and, particularly, the accumulation of organic mater in the moss-lichen layer and soil organic horizon on watersheds accounted for increasing mean DOC concentrations in the streams. In opposite, increased insulation of soils by organic matter accumulating on the soil surface leads to steadily decreasing ALT and constrains an infiltration of solutes to subsoil. As a result, inorganic solute loading to stream channels is tended to decrease during post-fire forest succession in permafrost affected terrains.

Patterns in DOC Concentration and Composition in Tundra Watersheds in the Kolyma River Basin

NASA Astrophysics Data System (ADS)

Behnke, M. I.; Schade, J. D.; Fiske, G. J.; Whittinghill, K. A.; Zimov, N.

2014-12-01

Much of the world's soil carbon is frozen in permafrost in the Arctic. As the climate warms and permafrost thaws, this carbon will again be actively cycled. Whether it is exported to the ocean or released as greenhouse gases to the atmosphere depends on the form of carbon compounds and conditions encountered during transport, and will determine the strength of permafrost thaw as a feedback on climate change. To better understand the fate of this carbon, we determined how and where in the landscape dissolved organic carbon (DOC) breaks down as water transports it from tundra to ocean. We compared DOC concentration and composition along flowpaths within watersheds and at the mouths of watersheds differing in drainage area. We incubated filtered water samples in light and dark, including filter-sterilized samples, to assess the interactions between light and microbial processing as mechanisms of DOC loss. Composition was assessed using optical measurements associated with the structure of organic compounds. DOC concentration declined along flowpaths within watersheds, with most loss occurring in aquatic environments high in the landscape. We also found a negative correlation between watershed size and DOC concentration. These results suggest that much of the processing of organic carbon occurs in small streams. In addition, the relationship with drainage area suggests that residence time in streams has a large impact on transformation of terrestrial carbon during transport. We found no substantial differences in optical characteristics of DOC, indicating that breakdown processes were not selective, and that light caused much of the breakdown. This conclusion is supported by the incubation experiment, which showed greater breakdown by light, and evidence that light stimulated higher rates of microbial processing. These results highlight the importance of inland aquatic ecosystems as processors of organic matter, and suggest that organic carbon from permafrost thaw is likely to be processed high in the landscape rather than transported to the ocean. Furthermore, the importance of light-induced breakdown as a mechanism for carbon loss suggests that the timing of DOC transport relative to seasonal changes in light intensity may influence the impact of permafrost thaw on climate change.

Using Eco-hydrologic modeling in the Penobscot River Watershed to explore the role of climate and land use change on DOC concentration and flux

NASA Astrophysics Data System (ADS)

Rouhani, S. F. B. B.; Schaaf, C.; Douglas, E. M.; Huntington, T. G.; Kim, J.

2017-12-01

Dissolved Organic Carbon leaches from the terrestrial watersheds to serve as one of the largest sources of marine DOC. Runoff, slope, soil organic matter and land cover characteristics are the primary spatial factors controlling the variability of fluvial Dissolved Organic Carbon fluxes through the catchment. In large, more heterogeneous catchments, streamflow dissolved organic carbon dynamics are regulated by the combined effect of hydrological mechanisms and the proportion of major landscape elements, such as wetland and forested areas. A number of studies have demonstrated that the amount of wetlands, especially peatlands, controls the watershed level transport of DOC in streams.The Penobscot River Watershed is located in north-central Maine and drains into the Gulf of Maine. It is the second largest watershed in New England. The Penobscot River Watershed is primarily forested but also contains extensive bogs, marshes, and wooded swamps.Studying the spatial and temporal changes in DOC export in the Penobscot River Watershed allows us to better understand and detect carbon sinks to carbon source shifts (or vice versa) in northern forested ecosystems.The Regional Hydro-Ecological Simulation System, is a physical process based terrestrial model that has the ability to simulate both the source and transportation of DOC by combining both hydrological and ecological processes. The study is focused on simulating the DOC concentration and flux with RHESSys in the Penobscot River Watershed. The simulated results are compared with field measurements of DOC from the watershed and the model results from the LOADEST and the temporal DOC export patterns are explored. Future changes in the amount of streamflow DOC will also be investigated by using projected land cover and climate change scenarios. Incremental increases in the loss of wetland areas have been implemented to explore the sensitivity of this watershed to wetland loss and progressive changes in forested land cover have been implemented to understand the role of vegetation types to the DOC flux.The simulated daily streamflow for the period of 2004-2013 corresponded well with observed daily streamflowat USGS gauge station. in addition, the simulated DOC flux and concentration values matched well with observed data and LODEST model results.

Seasonal Dynamics of Dissolved Organic Carbon Under Complex Circulation Schemes on a Large Continental Shelf: The Northern South China Sea

NASA Astrophysics Data System (ADS)

Meng, Feifei; Dai, Minhan; Cao, Zhimian; Wu, Kai; Zhao, Xiaozheng; Li, Xiaolin; Chen, Junhui; Gan, Jianping

2017-12-01

We examined the distribution and seasonality of dissolved organic carbon (DOC) based on a large data set collected from the northern South China Sea (NSCS) shelf under complex circulation schemes influenced by river plume, coastal upwelling, and downwelling. The highest surface values of ˜117 μmol L-1 were observed nearshore in summer suggesting high DOC supplies from the river inputs, whereas the lowest surface values of ˜62 μmol L-1 were on the outer shelf in winter due to entrainment of DOC-poor subsurface water under strengthened vertical mixing. While the summer coastal upwelling brought lower DOC from offshore depth to the nearshore surface, the winter coastal downwelling delivered higher surface DOC to the midshelf deep waters from the inner shelf fueled by the China Coastal Current (CCC) transporting relatively high DOC from the East China Sea to the NSCS. The intensified winter downwelling generated a cross-shelf DOC transport of 3.1 × 1012 g C over a large shelf area, which induced a significant depression of the NSCS DOC inventory in winter relative to in autumn. In addition to the variable physical controls, net biological production of DOC was semiquantified in both the river plume (2.8 ± 3.0 μmol L-1) and coastal upwelling (3.1 ± 1.3 μmol L-1) in summer. We demonstrated that the NSCS shelf had various origins of DOC including riverine inputs, inter-shelf transport and in situ production. Via cross-shelf transport, the accumulated DOC would be exported to and stored in the deep ocean, suggesting that continental shelves are a potentially effective carbon sink.

Dissolved organic matter properties in arctic coastal waters are strongly influenced by degrading permafrost coasts and by local meteorology.

NASA Astrophysics Data System (ADS)

Fritz, M.; Tanski, G.; Goncalves-Araujo, R.; Heim, B.; Koch, B.; Lantuit, H.

2016-12-01

Organic carbon and nutrients are increasingly mobilized from permafrost coasts due to accelerated coastal erosion in response to Arctic warming. The nearshore zone plays a crucial role in Arctic biogeochemical cycling, as here the released material is destined to be (1) mineralized into greenhouse gases, (2) incorporated into marine primary production, (3) buried in nearshore sediments or (4) transported offshore. We present dissolved organic matter (DOM) quantities in surface water in the nearshore zone of the southern Beaufort Sea from three consecutive summer seasons under different meteorological conditions. Colored and fluorescent dissolved organic matter (cDOM, fDOM) properties are used to differentiate the terrestrial from the marine DOM component. Dissolved organic carbon (DOC) concentrations in the nearshore zone of the southern Beaufort Sea vary between about 1.5 and 5 mg C L-1. In low salinity conditions between 8 and 15, high DOC concentrations of 3.5 to 5 mg C L-1prevail. Storm events can lead to strongly decreased DOC concentration and increasing salinity (14 to 28) in surface water, probably due to upwelling. In windy and wavy conditions throughout the season, the water column is well-mixed and DOC-poor because saline waters are transported from the offshore to the nearshore. We recognized a significant negative correlation between DOC and salinity, independent from varying meteorological conditions. This suggests conservative mixing between DOC derived from permafrost coasts and marine primary production. Stable stratification in the nearshore zone and calm weather conditions will increase the influence of terrestrial-derived DOM and the potential turnover time for biogeochemical cycling in coastal ecosystems. The strength of the terrestrial influence can be estimated by salinity and stable water isotope measures as they directly correlate with DOC concentrations; the lower the salinity the stronger the terrestrial influence. We conclude that the terrestrial footprint of coastal erosion on DOM concentrations in the nearshore zone is significant and may increase with future climate warming. Meteorological conditions play a major role for the strength of the terrestrial DOM signal, which can vary on short timescales.

Real Time Monitoring of Dissolved Organic Carbon Concentration and Disinfection By-Product Formation Potential in a Surface Water Treatment Plant with Simulaneous UV-VIS Absorbance and Fluorescence Excitation-Emission Mapping

NASA Astrophysics Data System (ADS)

Gilmore, A. M.

2015-12-01

This study describes a method based on simultaneous absorbance and fluorescence excitation-emission mapping for rapidly and accurately monitoring dissolved organic carbon concentration and disinfection by-product formation potential for surface water sourced drinking water treatment. The method enables real-time monitoring of the Dissolved Organic Carbon (DOC), absorbance at 254 nm (UVA), the Specific UV Absorbance (SUVA) as well as the Simulated Distribution System Trihalomethane (THM) Formation Potential (SDS-THMFP) for the source and treated water among other component parameters. The method primarily involves Parallel Factor Analysis (PARAFAC) decomposition of the high and lower molecular weight humic and fulvic organic component concentrations. The DOC calibration method involves calculating a single slope factor (with the intercept fixed at 0 mg/l) by linear regression for the UVA divided by the ratio of the high and low molecular weight component concentrations. This method thus corrects for the changes in the molecular weight component composition as a function of the source water composition and coagulation treatment effects. The SDS-THMFP calibration involves a multiple linear regression of the DOC, organic component ratio, chlorine residual, pH and alkalinity. Both the DOC and SDS-THMFP correlations over a period of 18 months exhibited adjusted correlation coefficients with r2 > 0.969. The parameters can be reported as a function of compliance rules associated with required % removals of DOC (as a function of alkalinity) and predicted maximum contaminant levels (MCL) of THMs. The single instrument method, which is compatible with continuous flow monitoring or grab sampling, provides a rapid (2-3 minute) and precise indicator of drinking water disinfectant treatability without the need for separate UV photometric and DOC meter measurements or independent THM determinations.

Tracking ultrasonically structural changes of natural aquatic organic carbon: Chemical fractionation and spectroscopic approaches.

PubMed

Al-Juboori, Raed A; Yusaf, Talal; Aravinthan, Vasantha; Bowtell, Leslie

2016-02-01

In this study, the structural alteration to DOC for a range of ultrasound treatments was investigated with chemical fractionation and UV-vis spectroscopic measurement. Ultrasound treatments were applied in continuous and pulsed modes at power levels of 48 and 84 W for effective treatment times of 5 and 15 min. Overall results show that the ultrasound treatments tended to degrade the hydrophobic aromatic fraction, while increasing the hydrophilic fraction to a lesser extent. The highest recorded reduction of hydrophobic DOC (17.8%) was achieved with pulse treatment of 84 W for15 min, while the highest increase in the hydrophilic DOC (10.5%) was obtained with continuous treatment at 84 W and 5 min. The optimal ultrasound treatment conditions were found to be pulse mode at high power and short treatment time, causing a minimal increase in the hydrophilic fraction of 1.3% with moderate removal of the hydrophobic fraction of 15.52%. The same treatment conditions, with longer treatment time, resulted in the highest removal of SUVA254 and SUVA280 of 17.09% and 16.93, respectively. These results indicate the potential for ultrasound treatments in DOC structural alteration. The hydrophobic fraction showed strong and significant correlations with UV absorbance at 254 and 280 nm. A254/A204 also exhibited strong and significant correlations with the hydrophobic/hydrophilic ratio. The other UV ratios (A250/A365 (E2/E3) and A254/A436) had weak and insignificant correlations with the hydrophobic/hydrophilic ratio. This confirms the applicability of UV indices as a suitable surrogate method for estimating the hydrophobic/hydrophilic structure. Copyright © 2015 Elsevier Ltd. All rights reserved.

Carbon dynamics in peatland pool systems: the role of light

NASA Astrophysics Data System (ADS)

Pickard, Amy; Heal, Kate; McLeod, Andy; Dinsmore, Kerry

2016-04-01

Open-water pools are widespread in peatlands and are considered to represent biogeochemical hotspots within the peatland landscape. However the contribution of pool systems to wider peatland C cycling has not been quantified fully and there is a lack of knowledge of the role of photochemical processes in such environments. In this study, light exposure experiments were conducted in two contrasting pools to test the reactivity of aquatic C. The first study site was located at Cross Lochs (CL), Forsinard, in the Flow Country of Northern Scotland, in a 412 m2 pool characterised by low dissolved organic carbon (DOC) concentrations (˜15 mg C L-1). The second site was located at Red Moss of Balerno (RM), a raised bog in central Scotland, in a 48 m2 pool with high DOC concentrations (˜35 mg C L-1). Experiments took place over 9 days in situ at each pool in mid-summer 2015, with 500 mL water samples contained in bags transparent to sunlight and in opaque control bags. After field exposure, optical, chemical and stable C isotope analyses were conducted on the samples. Significant differences in biogeochemical cycling of DOC were detected between the two systems, with DOC losses as a percentage of the total C pool 15% higher at RM than at CL after light exposure. The mean DOC concentration of light exposed samples at RM declined steeply initially, with 83% observed DOC degradation occurring by day 3 of the experiment. Total losses of 7.9 mg DOC L-1were observed in light exposed samples at RM, along with decreasing E4:E6 ratios, suggesting that material remaining at the end of the experiment was humified. Depletion of DOC was positively correlated with production of CO2 at both sites, with concentrations of up to 4.3 mg CO2-C L-1 recorded at RM. Stable C isotope signatures at both sites were altered under light treatment, as demonstrated by the production of enriched δ13C-DOC (+0.46 ‰ relative to opaque bags) and depleted δ13C-DIC (-0.97 ‰ relative to opaque bags) at RM. However, at CL, the δ13C-DOC signature in both the light exposed and opaque bags was depleted (-0.2‰ and -0.4 ‰ respectively), suggesting that microbial processing was the preferential DOC processing pathway in this system. These results show that C in peatland pools is highly reactive and further demonstrate the importance of photochemical processing of C, which should be considered as a significant driver of biogeochemical cycling.

A comparison of four porewater sampling methods for metal mixtures and dissolved organic carbon and the implications for sediment toxicity evaluations

USGS Publications Warehouse

Cleveland, Danielle; Brumbaugh, William G.; MacDonald, Donald D.

2017-01-01

Evaluations of sediment quality conditions are commonly conducted using whole-sediment chemistry analyses but can be enhanced by evaluating multiple lines of evidence, including measures of the bioavailable forms of contaminants. In particular, porewater chemistry data provide information that is directly relevant for interpreting sediment toxicity data. Various methods for sampling porewater for trace metals and dissolved organic carbon (DOC), which is an important moderator of metal bioavailability, have been employed. The present study compares the peeper, push point, centrifugation, and diffusive gradients in thin films (DGT) methods for the quantification of 6 metals and DOC. The methods were evaluated at low and high concentrations of metals in 3 sediments having different concentrations of total organic carbon and acid volatile sulfide and different particle-size distributions. At low metal concentrations, centrifugation and push point sampling resulted in up to 100 times higher concentrations of metals and DOC in porewater compared with peepers and DGTs. At elevated metal levels, the measured concentrations were in better agreement among the 4 sampling techniques. The results indicate that there can be marked differences among operationally different porewater sampling methods, and it is unclear if there is a definitive best method for sampling metals and DOC in porewater.

Sources, distributions and dynamics of dissolved organic matter in the Canada and Makarov Basins

USGS Publications Warehouse

Shen, Yuan; Benner, Ronald; Robbins, Lisa L.; Wynn, Jonathan

2016-01-01

A comprehensive survey of dissolved organic carbon (DOC) and chromophoric dissolved organic matter (CDOM) was conducted in the Canada and Makarov Basins and adjacent seas during 2010–2012 to investigate the dynamics of dissolved organic matter (DOM) in the Arctic Ocean. Sources and distributions of DOM in polar surface waters were very heterogeneous and closely linked to hydrological conditions. Canada Basin surface waters had relatively low DOC concentrations (69 ± 6 μmol L−1), CDOM absorption (a325: 0.32 ± 0.07 m−1) and CDOM-derived lignin phenols (3 ± 0.4 nmol L−1), and high spectral slope values (S275–295: 31.7 ± 2.3 μm−1), indicating minor terrigenous inputs and evidence of photochemical alteration in the Beaufort Gyre. By contrast, surface waters of the Makarov Basin had elevated DOC (108 ± 9 μmol L−1) and lignin phenol concentrations (15 ± 3 nmol L−1), high a325 values (1.36 ± 0.18 m−1), and low S275–295 values (22.8 ± 0.8 μm−1), indicating pronounced Siberian river inputs associated with the Transpolar Drift and minor photochemical alteration. Observations near the Mendeleev Plain suggested limited interactions of the Transpolar Drift with Canada Basin waters, a scenario favoring export of Arctic DOM to the North Atlantic. The influence of sea-ice melt on DOM was region-dependent, resulting in an increase (Beaufort Sea), a decrease (Bering-Chukchi Seas), and negligible change (deep basins) in surface DOC concentrations and a325 values. Halocline structures differed between basins, but the Canada Basin upper halocline and Makarov Basin halocline were comparable in their average DOC (65–70 μmol L−1) and lignin phenol concentrations (3–4 nmol L−1) and S275–295 values (22.9–23.7 μm−1). Deep-water DOC concentrations decreased by 6–8 μmol L−1 with increasing depth, water mass age, nutrient concentrations, and apparent oxygen utilization. Maximal estimates of DOC degradation rates (0.036–0.039 μmol L−1 yr−1) in the deep Arctic were lower than those in other ocean basins, possibly due to low water temperatures. DOC concentrations in bottom waters (>2500 m; 46 ± 2 μmol L−1) of the Canada and Makarov Basins were slightly lower than those reported for deep waters of the Eurasian Basin and Nordic Seas. Elevated a325 values (by 10–20%) were observed near the seafloor, indicating biological activity in Arctic basin sediments.

Mercury photoreduction and photooxidation in lakes: Effects of filtration and dissolved organic carbon concentration.

PubMed

O'Driscoll, Nelson J; Vost, Emma; Mann, Erin; Klapstein, Sara; Tordon, Robert; Lukeman, Matthew

2018-06-01

Mercury is a globally distributed, environmental contaminant. Quantifying the retention and loss of mercury is integral for predicting mercury-sensitive ecosystems. There is little information on how dissolved organic carbon (DOC) concentrations and particulates affect mercury photoreaction kinetics in freshwater lakes. To address this knowledge gap, samples were collected from ten lakes in Kejimkujik National Park, Nova Scotia (DOC: 2.6-15.4mg/L). Filtered (0.2μm) and unfiltered samples were analysed for gross photoreduction, gross photooxidation, and net reduction rates of mercury using pseudo first-order curves. Unfiltered samples had higher concentrations (p=0.04) of photoreducible divalent mercury (Hg(II) RED ) (mean of 754±253pg/L) than filtered samples (mean of 482±206pg/L); however, gross photoreduction and photooxidation rate constants were not significantly different in filtered or unfiltered samples in early summer. DOC was not significantly related to gross photoreduction rate constants in filtered (R 2 =0.43; p=0.08) and unfiltered (R 2 =0.02; p=0.71) samples; DOC was also not significantly related to gross photooxidation rate constants in filtered or unfiltered samples. However, DOC was significantly negatively related with Hg(II) RED in unfiltered (R 2 =0.53; p=0.04), but not in filtered samples (R 2 =0.04; p=0.60). These trends indicate that DOC is a factor in determining dissolved mercury photoreduction rates and particles partially control available Hg(II) RED in lake water. This research also demonstrates that within these lakes gross photoreduction and photooxidation processes are close to being in balance. Changes to catchment inputs of particulate matter and DOC may alter mercury retention in these lakes and could partially explain observed increases of mercury accumulation in biota. Copyright © 2017. Published by Elsevier B.V.

Effects of Land Use on Stable Carbon Isotopic Composition and Concentration of Dissolved Organic Carbon (DOC) and Dissolved Inorganic Carbon (DIC) in Southeastern US Piedmont Headwater Streams

EPA Science Inventory

Stable carbon isotopic composition (delta 13C) and concentrations of DOC and DIC were measured in stream water samples collected monthly in 15 headwater streams from an area with extensive poultry and cattle production and a rapidly growing human population. Linear regression te...

Integrated bicarbonate-form ion exchange treatment and regeneration for DOC removal: Model development and pilot plant study.

PubMed

Hu, Yue; Boyer, Treavor H

2017-05-15

The application of bicarbonate-form anion exchange resin and sodium bicarbonate salt for resin regeneration was investigated in this research is to reduce chloride ion release during treatment and the disposal burden of sodium chloride regeneration solution when using traditional chloride-form ion exchange (IX). The target contaminant in this research was dissolved organic carbon (DOC). The performance evaluation was conducted in a completely mixed flow reactor (CMFR) IX configuration. A process model that integrated treatment and regeneration was investigated based on the characteristics of configuration. The kinetic and equilibrium experiments were performed to obtain required parameters for the process model. The pilot plant tests were conducted to validate the model as well as provide practical understanding on operation. The DOC concentration predicted by the process model responded to the change of salt concentration in the solution, and showed a good agreement with pilot plant data with less than 10% difference in terms of percentage removal. Both model predictions and pilot plant tests showed over 60% DOC removal by bicarbonate-form resin for treatment and sodium bicarbonate for regeneration, which was comparable to chloride-form resin for treatment and sodium chloride for regeneration. Lastly, the DOC removal was improved by using higher salt concentration for regeneration. Copyright © 2017 Elsevier Ltd. All rights reserved.

Deoxycholate-hydrogels: novel drug carrier systems for topical use.

PubMed

Valenta, C; Nowack, E; Bernkop-Schnürch, A

1999-08-05

Na-deoxycholate (Na-DOC) forms a viscous thixotropic gel when in contact with excess buffer systems. The resulting gels have been tested as novel drug carrier systems for topical use. The influence of differing amounts of mannitol, glycerol and xylitol on the viscous modulus (G"/Pa) was evaluated by oscillatory measurements. Na-DOC (0.5%) in phosphate buffered saline (PBS) with 5% mannitol was chosen as an optimised formulation, taking into account viscosity, distribution and appearance. The release rate of the model drug rutin through an artificial membrane was higher than those from hydroxyethylcellulose- (HEC) and sodium polyacrylate (NaC934)-gels; permeation through excised rat skin was also highest for the Na-DOC systems. The results indicate that Na-DOC significantly increases the membrane permeability. The microbial stability was in the same range as HEC- and NaC934-gels, making a preservation necessary. Na-DOC-gels are novel low molecular weight, multifunctional drug carriers, which also act as penetration enhancers. Their thixotropy is an additional advantage for better application to large skin areas, nasal, vaginal and buccal membranes. Therefore, Na-DOC-gels can be considered promising, alternative drug carrier systems for topical pharmaceutical as well as cosmetic use.

Compositionally heterogeneous dissolved organic matter reflects changing flowpaths in a large ice sheet catchment over the course of the melt season at Leverett Glacier, southwest Greenland

NASA Astrophysics Data System (ADS)

Kellerman, A.; Hawkings, J.; Marshall, M.; Spencer, R.; Wadham, J.

2017-12-01

The Greenland Ice Sheet (GrIS) is losing mass at a remarkable rate. This loss of mass coincides with the export of dissolved organic matter (DOM) and other nutrients from the ice sheet and exerts a primary control on secondary production in downstream ecosystems. However, little is known about the source and composition of DOM exported from these dilute, yet immense, systems. Samples were collected from May 11, 2015 to July 29, 2015 from the outflow of Leverett Glacier, a large, land-terminating glacier of the southwest GrIS. Dissolved organic carbon (DOC) concentrations were measured and the optical properties of DOM were characterized using absorbance and fluorescence spectroscopy. At the beginning of the season, when discharge is <5 m3 sec-1, red-shifted fluorescence suggests terrestrial inputs from either overridden soils or proglacial inputs dominate the DOM pool. With the onset of melt, after an initial pulse in both DOC quantity and red-shifted fluorescence intensity, the DOC concentration and fluorescence intensity is diluted, with little change in DOM composition. The terrestrial signal is lost with the first outburst event in late June, and a single protein-like fluorophore is exhibited for three weeks. On July 10th, a fourth outburst event introduces a second protein-like fluorophore, indicative of production on the ice sheet, and this signature is maintained until the end of the July. These results suggest that subglaical drainage flowpaths and water source influence the exported DOC concentration and DOM composition over a summer melt season. As glacial outflow shifts from higher DOC concentrations early in the season to low DOC concentrations later in the summer, these results impact estimates of carbon export from glaciers. Furthermore, as composition is related to reactivity, the compositional changes observed may indicate shifts in the bioavailability of the DOM upon delivery to coastal systems, a result of changing DOM sources over the course of the season.

The effectiveness of arbuscular-mycorrhizal fungi and Aspergillus niger or Phanerochaete chrysosporium treated organic amendments from olive residues upon plant growth in a semi-arid degraded soil.

PubMed

Medina, A; Roldán, A; Azcón, R

2010-12-01

Arbuscular mycorrhizal (AM) fungi and a residue from dry olive cake (DOC) supplemented with rock phosphate (RP) and treated with either Aspergillus niger (DOC-A) or Phanerochaete chrysosporium (DOC-P), were assayed in a natural, semi-arid soil using Trifolium repens or Dorycnium pentaphyllum plants. The effects of the AM fungi and/or DOC-A were compared with P-fertilisation (P) over eleven successive harvests to evaluate the persistence of the effectiveness of the treatments. The biomass of dually-treated plants after four successive harvests was greater than that obtained for non-treated plants or those receiving the AM inoculum or DOC-A treatments after eleven yields. The AM inoculation was critical for obtaining plant growth benefit from the application of fermented DOC-A residue. The abilities of the treatments to prevent plant drought stress were also assayed. Drought-alleviating effects were evaluated in terms of plant growth, proline and total sugars concentration under alternative drought and re-watering conditions (8th and 9th harvests). The concentrations of both compounds in plant biomass increased under drought when DOC-A amendment and AM inoculation were employed together: they reinforced the plant drought-avoidance capabilities and anti-oxidative defence. Water stress was less compensated in P-fertilised than in DOC-A-treated plants. DOC-P increased D. pentaphyllum biomass, shoot P content, nodule number and AM colonisation, indicating the greater DOC-transforming ability of P. chrysosporium compared to A. niger. The lack of AM colonisation and nodulation in this soil was compensated by the application of DOC-P, particularly with AM inoculum. The management of natural resources (organic amendments and soil microorganisms) represents an important strategy that assured the growth, nutrition and plant establishment in arid, degraded soils, preventing the damage that arises from limited water and nutrient supply. Copyright © 2010 Elsevier Ltd. All rights reserved.

Dynamics of dissolved organic carbon (DOC) through stormwater basins designed for groundwater recharge in urban area: Assessment of retention efficiency.

PubMed

Mermillod-Blondin, Florian; Simon, Laurent; Maazouzi, Chafik; Foulquier, Arnaud; Delolme, Cécile; Marmonier, Pierre

2015-09-15

Managed aquifer recharge (MAR) has been developed in many countries to limit the risk of urban flooding and compensate for reduced groundwater recharge in urban areas. The environmental performances of MAR systems like infiltration basins depend on the efficiency of soil and vadose zone to retain stormwater-derived contaminants. However, these performances need to be finely evaluated for stormwater-derived dissolved organic matter (DOM) that can affect groundwater quality. Therefore, this study examined the performance of MAR systems to process DOM during its transfer from infiltration basins to an urban aquifer. DOM characteristics (fluorescent spectroscopic properties, biodegradable and refractory fractions of dissolved organic carbon -DOC-, consumption by micro-organisms during incubation in slow filtration sediment columns) were measured in stormwater during its transfer through three infiltration basins during a stormwater event. DOC concentrations sharply decreased from surface to the aquifer for the three MAR sites. This pattern was largely due to the retention of biodegradable DOC which was more than 75% for the three MAR sites, whereas the retention of refractory DOC was more variable and globally less important (from 18% to 61% depending on MAR site). Slow filtration column experiments also showed that DOC retention during stormwater infiltration through soil and vadose zone was mainly due to aerobic microbial consumption of the biodegradable fraction of DOC. In parallel, measurements of DOM characteristics from groundwaters influenced or not by MAR demonstrated that stormwater infiltration increased DOC quantity without affecting its quality (% of biodegradable DOC and relative aromatic carbon content -estimated by SUVA254-). The present study demonstrated that processes occurring in soil and vadose zone of MAR sites were enough efficient to limit DOC fluxes to the aquifer. Nevertheless, the enrichments of DOC concentrations measured in groundwater below infiltration basins need to be considered in future studies to especially assess their impact on groundwater quality. Copyright © 2015 Elsevier Ltd. All rights reserved.

Decreasing DOC trends in soil solution along the hillslopes at two IM sites in southern Sweden--geochemical modeling of organic matter solubility during acidification recovery.

PubMed

Löfgren, Stefan; Gustafsson, Jon Petter; Bringmark, Lage

2010-12-01

Numerous studies report increased concentrations of dissolved organic carbon (DOC) during the last two decades in boreal lakes and streams in Europe and North America. Recently, a hypothesis was presented on how various spatial and temporal factors affect the DOC dynamics. It was concluded that declining sulphur deposition and thereby increased DOC solubility, is the most important driver for the long-term DOC concentration trends in surface waters. If this recovery hypothesis is correct, the DOC levels should increase both in the soil solution as well as in the surrounding surface waters as soil pH rises and the ionic strength declines due to the reduced input of SO(4)(2-) ions. In this project a geochemical model was set up to calculate the net humic charge and DOC solubility trends in soils during the period 1996-2007 at two integrated monitoring sites in southern Sweden, showing clear signs of acidification recovery. The Stockholm Humic Model was used to investigate whether the observed DOC solubility is related to the humic charge and to examine how pH and ionic strength influence it. Soil water data from recharge and discharge areas, covering both podzols and riparian soils, were used. The model exercise showed that the increased net charge following the pH increase was in many cases counteracted by a decreased ionic strength, which acted to decrease the net charge and hence the DOC solubility. Thus, the recovery from acidification does not necessarily have to generate increasing DOC trends in soil solution. Depending on changes in pH, ionic strength and soil Al pools, the trends might be positive, negative or indifferent. Due to the high hydraulic connectivity with the streams, the explanations to the DOC trends in surface waters should be searched for in discharge areas and peat lands. Copyright © 2010 Elsevier B.V. All rights reserved.

Effects of High Dissolved Inorganic and Organic Carbon Availability on the Physiology of the Hard Coral Acropora millepora from the Great Barrier Reef

PubMed Central

Meyer, Friedrich W.; Vogel, Nikolas; Diele, Karen; Kunzmann, Andreas; Uthicke, Sven; Wild, Christian

2016-01-01

Coral reefs are facing major global and local threats due to climate change-induced increases in dissolved inorganic carbon (DIC) and because of land-derived increases in organic and inorganic nutrients. Recent research revealed that high availability of labile dissolved organic carbon (DOC) negatively affects scleractinian corals. Studies on the interplay of these factors, however, are lacking, but urgently needed to understand coral reef functioning under present and near future conditions. This experimental study investigated the individual and combined effects of ambient and high DIC (pCO2 403 μatm/ pHTotal 8.2 and 996 μatm/pHTotal 7.8) and DOC (added as Glucose 0 and 294 μmol L-1, background DOC concentration of 83 μmol L-1) availability on the physiology (net and gross photosynthesis, respiration, dark and light calcification, and growth) of the scleractinian coral Acropora millepora (Ehrenberg, 1834) from the Great Barrier Reef over a 16 day interval. High DIC availability did not affect photosynthesis, respiration and light calcification, but significantly reduced dark calcification and growth by 50 and 23%, respectively. High DOC availability reduced net and gross photosynthesis by 51% and 39%, respectively, but did not affect respiration. DOC addition did not influence calcification, but significantly increased growth by 42%. Combination of high DIC and high DOC availability did not affect photosynthesis, light calcification, respiration or growth, but significantly decreased dark calcification when compared to both controls and DIC treatments. On the ecosystem level, high DIC concentrations may lead to reduced accretion and growth of reefs dominated by Acropora that under elevated DOC concentrations will likely exhibit reduced primary production rates, ultimately leading to loss of hard substrate and reef erosion. It is therefore important to consider the potential impacts of elevated DOC and DIC simultaneously to assess real world scenarios, as multiple rather than single factors influence key physiological processes in coral reefs. PMID:26959499

Effects of High Dissolved Inorganic and Organic Carbon Availability on the Physiology of the Hard Coral Acropora millepora from the Great Barrier Reef.

PubMed

Meyer, Friedrich W; Vogel, Nikolas; Diele, Karen; Kunzmann, Andreas; Uthicke, Sven; Wild, Christian

2016-01-01

Coral reefs are facing major global and local threats due to climate change-induced increases in dissolved inorganic carbon (DIC) and because of land-derived increases in organic and inorganic nutrients. Recent research revealed that high availability of labile dissolved organic carbon (DOC) negatively affects scleractinian corals. Studies on the interplay of these factors, however, are lacking, but urgently needed to understand coral reef functioning under present and near future conditions. This experimental study investigated the individual and combined effects of ambient and high DIC (pCO2 403 μatm/ pHTotal 8.2 and 996 μatm/pHTotal 7.8) and DOC (added as Glucose 0 and 294 μmol L-1, background DOC concentration of 83 μmol L-1) availability on the physiology (net and gross photosynthesis, respiration, dark and light calcification, and growth) of the scleractinian coral Acropora millepora (Ehrenberg, 1834) from the Great Barrier Reef over a 16 day interval. High DIC availability did not affect photosynthesis, respiration and light calcification, but significantly reduced dark calcification and growth by 50 and 23%, respectively. High DOC availability reduced net and gross photosynthesis by 51% and 39%, respectively, but did not affect respiration. DOC addition did not influence calcification, but significantly increased growth by 42%. Combination of high DIC and high DOC availability did not affect photosynthesis, light calcification, respiration or growth, but significantly decreased dark calcification when compared to both controls and DIC treatments. On the ecosystem level, high DIC concentrations may lead to reduced accretion and growth of reefs dominated by Acropora that under elevated DOC concentrations will likely exhibit reduced primary production rates, ultimately leading to loss of hard substrate and reef erosion. It is therefore important to consider the potential impacts of elevated DOC and DIC simultaneously to assess real world scenarios, as multiple rather than single factors influence key physiological processes in coral reefs.

After the flood: consistency in DOM response to the 2010/2011 Australian floods

NASA Astrophysics Data System (ADS)

Shutova, Y.; Baker, A.; Bridgeman, J.; Henderson, R.

2014-12-01

The 2010/2011 floods in Eastern Australia were one of the worst on record, causing more than one billion AUD of damages and killing 35 people. This field campaign, monitoring raw water DOM concentration and character on three contrasting rivers across the region captured the late recession curve (October 2011- September 2012). DOM was characterized using fluorescence excitation-emission matrix (EEM) spectra with PARAFAC analysis; δ 13C-DOC; and molecular size using liquid chromatography with organic carbon, UV254 and nitrogen detection (LC-OCD) to identify DOC fractions: biopolymers, humic substance (HS), building blocks (BB), low molecular weight acids, and low molecular weight neutrals. Despite the difference in catchment and climatic zones, similar trends were observed in all three rivers, where DOC concentrations gradually decreased in river streams over a year from 8-11 mgCL-1 to 3-4 mgCL-1, followed by similar changes of HS, BB and fluorescent terrestrially delivered DOM components (C1-C3). In Allyn and Patterson rivers the proportion of HS, fluorescent terrestrially delivered DOM components (C1, C2) in DOC have decreased, in contrast to Logan River, where the ratio of HS/DOC was highly variable and showed no particular trends. The proportion of other DOC components remained almost the same. Molecular weight of the HS declined from 700 gmol-1 to 610 gmol-1 in all sites. δ 13C-DOC increased during monitoring, this could be linked to general decrease of DOM proportion delivered from C4 type plants after the flood. Overall, although DOC concentration decreased over the year post flood at all sites, most importantly the composition of DOM changed, with major changes occurring in proportion of humic-like and fluorescent terrestrially delivered DOM. Therefore it is important to monitor DOM character to be able to assess the impact of climate change and extreme weather events on the DOM transport and transformation.

Bamboo biochar amendment improves the growth and reproduction of Eisenia fetida and the quality of green waste vermicompost.

PubMed

Gong, Xiaoqiang; Cai, Linlin; Li, Suyan; Chang, Scott X; Sun, Xiangyang; An, Zhengfeng

2018-07-30

Vermicomposting is a promising method for reusing urban green waste. However, high lignin content in the green waste could hinder the development of earthworm and microorganisms and the vermicomposting process, resulting in a low-quality vermicompost product. The objective of this study was to evaluate the effect of bamboo biochar addition (at 0%, 3%, and 6% on a dry w/w basis) on the activity of Eisenia fetida and the obtained vermicompost. Biochar addition increased (P < 0.05) earthworm biomass, juvenile and cocoon numbers of Eisenia fetida, as well as the activities of dehydrogenase, cellulase, urease and alkaline phosphatase. Compared to the control, lignin degradation rate was enhanced up to 13.89% by biochar addition. Biochar addition also improved the vermicompost quality in terms of cation exchange capacity (CEC), dissolved organic carbon (DOC) degradation, humification, nitrogen transformation, toxicity to germinating seeds (Brassica rapa L., Chinensis group) and heavy metals concentrations. The 6% bamboo biochar addition rate achieved maturity after 60 days of vermicomposting and resulted in the highest quality vermicompost based on parameters such as CEC, DOC, NH 4 + -N/NO 3 - -N ratio, germination index and heavy metal concentration. We conclude that 6% biochar addition promoted earthworm growth and the vermicomposting of green waste. Copyright © 2018 Elsevier Inc. All rights reserved.

Effects of Aftermarket Control Technologies on Gas and ...

EPA Pesticide Factsheets

Particulate matter (PM) originating from diesel combustion is a public health concern due to its association with adverse effects on respiratory and cardiovascular diseases and lung cancer. This study investigated emissions from three stationary diesel engines (gensets) with varying power output (230 kW, 400 kW, and 600 kW) at 50% and 90% load to determine concentrations of gaseous (GROS) and PM reactive oxygen species (PMROS). In addition, the influence of three modern emission control technologies on ROS emissions was evaluated: active and passive diesel particulate filters (A-DPF and P-DPF) and a diesel oxidation catalyst (DOC). PMROS made up 30-50% of the total ROS measured without aftermarket controls. All applied controls removed PMROS by more than 75% on average. However, the oxidative potential of PM downstream of these devices was not diminished at the same rate and particles surviving the A-PDF had an even higher oxidative potential on a per PM mass basis compared to the particles emitted by uncontrolled gensets. Further, the GROS as compared to PMROS emissions were not reduced with the same efficiency (<36%). GROS concentrations were highest with the DOC in use, indicating continued formation of GROS with this control. Correlation analyses showed that PMROS and to a lesser extent GROS have a good correlation with semi-volatile organic carbon (OC1) sub-fraction. In addition, results suggest that chemical composition, rather than PM size, is re

Effect of nitrate and ammonium fertilization on Zn, Pb, and Cd phytostabilization by Populus euramericana Dorskamp in contaminated technosol.

PubMed

Qasim, Bashar; Motelica-Heino, Mikael; Bourgerie, Sylvain; Gauthier, Arnaud; Morabito, Domenico

2015-12-01

This study aimed at assessing the effect of nitrogen addition under two forms, nitrate and ammonium, on the stabilization of Zn, Pb, and Cd by Populus euramericana Dorskamp grown in contaminated soils for 35 days under controlled conditions. Temporal changes in the soil pore water (SPW) were monitored for pH, dissolved organic carbon (DOC), and total dissolved concentrations of metals in the soils rhizosphere. Rhizospheric SPW pH decreased gradually with NH4(+) addition and increased with NO3(-) addition up to one unit, while it slightly decreased initially then increased for the untreated control soil DOC increased with time up to six times, the highest increase occurring with NH4(+) fertilization. An increase in the metal concentrations in the rhizospheric SPW was observed for NH4(+) addition associated with the lowest rhizospheric SPW pH, whereas the opposite was observed for the control soil and NO3(-) fertilization. Fertilization did not affect plant shoots or roots biomass development compared to the untreated control (without N addition). Metals were mostly accumulated in the rhizosphere and N fertilization increased the accumulation for Zn and Pb while Cd accumulation was enhanced for NH4(+) addition. Collectively, our results suggest metal stabilization by P. euramericana Dorskamp rhizosphere with nitrogen fertilization and are potential for phytostabilization of contaminated technosol.

Relationship between nutrients and plankton biomass in the turbidity maximum zone of the Pearl River Estuary.

PubMed

Shi, Zhen; Xu, Jie; Huang, Xiaoping; Zhang, Xia; Jiang, Zhijian; Ye, Feng; Liang, Ximei

2017-07-01

Nutrients, dissolved and particulate organic carbon and plankton (bacterio-, phyto- and zoo-) were compared in the turbidity maximum zone (TMZ) and adjacent areas (non-TMZ) in the Pearl River estuary. Our results showed that high levels of suspended substances had marked effect on dynamics of nutrients and plankton in the TMZ. Based on the cluster analysis of total suspended solids (TSS) concentrations, all stations were divided into two groups, TMZ with average TSS of 171mg/L and non-TMZ of 45mg/L. Suspended substances adsorbed PO 4 3- and dissolved organic carbon, resulting in higher particulate phosphorus and organic carbon (POC) and lower PO 4 3- and DOC in the TMZ, compared to the non-TMZ. However, suspended substances had limited effect on nitrogenous nutrients. Phytoplankton growth was light-limited due to high concentrations of suspended substances in the TMZ and a peak of phytoplankton abundance appeared in the non-TMZ. In contrast, the highest bacterial abundance occurred in the TMZ, which was likely partly responsible for low DOC levels. Two peaks of zooplankton abundance observed in the TMZ and non-TMZ in the Pearl River estuary were primarily supported by bacteria and phytoplankton, respectively. Our finding implied that high levels of suspended solids in the TMZ affect the trophic balance. Copyright © 2016. Published by Elsevier B.V.

Copper speciation and binding by organic matter in copper-contaminated streamwater

USGS Publications Warehouse

Breault, R.F.; Colman, J.A.; Aiken, G.R.; McKnight, D.

1996-01-01

Fulvic acid binding sites (1.3-70 ??M) and EDTA (0.0017-0.18 ??M) accounted for organically bound Cu in seven stream samples measured by potentiometric titration. Cu was 84-99% organically bound in filtrates with 200 nM total Cu. Binding of Cu by EDTA was limited by competition from other trace metals. Water hardness was inversely related to properties of dissolved organic carbon (DOC) that enhance fulvic acid binding: DOC concentration, percentage of DOC that is fulvic acid, and binding sites per fulvic acid carbon. Dissolved trace metals, stabilized by organic binding, occurred at increased concentration in soft water as compared to hard water.

Spatiotemporal drivers of dissolved organic matter in high alpine lakes: Role of Saharan dust inputs and bacterial activity.

PubMed

Mladenov, Natalie; Pulido-Villena, Elvira; Morales-Baquero, Rafael; Ortega-Retuerta, Eva; Sommaruga, Ruben; Reche, Isabel

2008-01-01

The effects of many environmental stressors such as UV radiation are mediated by dissolved organic matter (DOM) properties. Therefore, determining the factors shaping spatial and temporal patterns is particularly essential in the most susceptible, low dissolved organic carbon (DOC) lakes. We analyzed spatiotemporal variations in dissolved organic carbon concentration and dissolved organic matter optical properties (absorption and fluorescence) in 11 transparent lakes located above tree line in the Sierra Nevada Mountains (Spain), and we assessed potential external (evaporation and atmospheric deposition) and internal (bacterial abundance, bacterial production, chlorophyll a, and catchment vegetation) drivers of DOM patterns. At spatial and temporal scales, bacteria were related to chromophoric DOM (CDOM). At the temporal scale, water soluble organic carbon (WSOC) in dust deposition and evaporation were found to have a significant influence on DOC and CDOM in two Sierra Nevada lakes studied during the ice-free periods of 2000-2002. DOC concentrations and absorption coefficients at 320 nm were strongly correlated over the spatial scale (n = 11, R(2) = 0.86; p < 0.01), but inconsistently correlated over time, indicating seasonal and interannual variability in external factors and a differential response of DOC concentration and CDOM to these factors. At the continental scale, higher mean DOC concentrations and more CDOM in lakes of the Sierra Nevada than in lakes of the Pyrenees and Alps may be due to a combination of more extreme evaporation, and greater atmospheric dust deposition.

Spatiotemporal drivers of dissolved organic matter in high alpine lakes: Role of Saharan dust inputs and bacterial activity

PubMed Central

Mladenov, Natalie; Pulido-Villena, Elvira; Morales-Baquero, Rafael; Ortega-Retuerta, Eva; Sommaruga, Ruben; Reche, Isabel

2010-01-01

The effects of many environmental stressors such as UV radiation are mediated by dissolved organic matter (DOM) properties. Therefore, determining the factors shaping spatial and temporal patterns is particularly essential in the most susceptible, low dissolved organic carbon (DOC) lakes. We analyzed spatiotemporal variations in dissolved organic carbon concentration and dissolved organic matter optical properties (absorption and fluorescence) in 11 transparent lakes located above tree line in the Sierra Nevada Mountains (Spain), and we assessed potential external (evaporation and atmospheric deposition) and internal (bacterial abundance, bacterial production, chlorophyll a, and catchment vegetation) drivers of DOM patterns. At spatial and temporal scales, bacteria were related to chromophoric DOM (CDOM). At the temporal scale, water soluble organic carbon (WSOC) in dust deposition and evaporation were found to have a significant influence on DOC and CDOM in two Sierra Nevada lakes studied during the ice-free periods of 2000–2002. DOC concentrations and absorption coefficients at 320 nm were strongly correlated over the spatial scale (n = 11, R2 = 0.86; p < 0.01), but inconsistently correlated over time, indicating seasonal and interannual variability in external factors and a differential response of DOC concentration and CDOM to these factors. At the continental scale, higher mean DOC concentrations and more CDOM in lakes of the Sierra Nevada than in lakes of the Pyrenees and Alps may be due to a combination of more extreme evaporation, and greater atmospheric dust deposition. PMID:20582227

Lake size and water-column stability affect the importance of methane for pelagic food webs of boreal lakes

NASA Astrophysics Data System (ADS)

Kankaala, Paula; Lopez-Bellido, Jessica; Ojala, Anne; Tulonen, Tiina; Jones, Roger I.

2013-04-01

Physical forcing, related to lake size and morphometry, plays an important role in the landscape-scale biogeochemical processing and fluxes of terrestrial carbon in lakes. Boreal lakes are typically dimictic, with mixing of the water column in spring and autumn, but in small, sheltered, humic, forest lakes the spring mixing is often incomplete. This leads to a steep summer stratification and oxygen depletion in the hypolimnion of the lakes. As a result of anaerobic decomposition of organic matter, high concentrations of CH4are typical in these lakes. At the oxic-anoxic interface zone methanotrophic microbes oxidize CH4 to CO2 and partly incorporate CH4-C into microbial biomass, and thus potentially provide a diet source for pelagic consumers. We studied production at the base of the pelagic food web by methane oxidising bacteria (MOB), heterotrophic bacteria (HB) and phytoplankton (PP) in five boreal lakes with a dissolved organic carbon (DOC) concentration varying between 7 and 25 mg C L-1 and an area ranging from 0.004 to 13.4 km2. High MOB activity was detected in the water columns of the three smallest lakes having anoxia in the hypolimnion during summer. The highest MOB activities (ca. 2-12 μmol L-1 d-1) were observed when the CH4:O2 ratio varied between ca. 0.5-12. Seasonally, the highest MOB activities were measured during late-summer mixed layer deepening and autumnal mixing of the whole water column. The proportion of MOB in the total basal production was highest in the two smallest lakes (24-56 and 13-36%), having the steepest summertime stratification. The proportion MOB in the basal production decreased with lake size being 70% of basal production was by PP. In all studied lakes HB contributed only 10-23% of the total basal production, suggesting that a transfer of allochthonous DOC via HB plays only a modest role for the nutrition of the higher trophic levels.

Source water controls on the character and origin of dissolved organic matter in streams of the Yukon River basin, Alaska

Treesearch

Jonathan A. O' Donnell; George R. Aiken; Evan S. Kane; Jeremy B. Jones

2010-01-01

Climate warming and permafrost degradation at high latitudes will likely impact watershed hydrology, and consequently, alter the concentration and character of dissolved organic carbon (DOC) in northern rivers. We examined seasonal variation of DOC chemistry in 16 streams of the Yukon River basin, Alaska. Our primary objective was to evaluate DOC chemical composition....

Low dose combinations of 2-methoxyestradiol and docetaxel block prostate cancer cells in mitosis and increase apoptosis.

PubMed

Reiner, Teresita; de las Pozas, Alicia; Gomez, Lourdes A; Perez-Stable, Carlos

2009-04-08

Clinical trials have shown that chemotherapy with docetaxel (Doc) combined with prednisone can improve survival of patients with androgen-independent prostate cancer (AI-PC). It is likely that the combination of Doc with other novel agents would also improve the survival of AI-PC patients. We investigated whether the combination of Doc and 2-methoxyestradiol (2ME2), an endogenous metabolite of estradiol promising for cancer therapy, can increase apoptotic cell death in prostate cancer cells. Low concentration 2ME2 (0.5-1 microM)+Doc (0.05-0.1 nM) combinations inhibit cell growth, increase G2/M cell cycle arrest, and increase apoptosis more effectively than the single concentrations in a variety of human AI-PC cells. Effects on apoptosis were associated with an increase in p53 protein and a decrease in cyclin A-dependent kinase activity. We then investigated whether the combination of 2ME2+Doc can increase apoptotic cell death and inhibit the growth of prostate tumors in the FG/Tag transgenic mouse model of AI-PC. Doses of 2ME2 and Doc that increase mitotic cell cycle arrest result in an increase in apoptosis and lower primary prostate tumor weights in FG/Tag mice. High dose 2ME2+Doc combinations did not increase G2/M cell cycle arrest or apoptosis in AI-PC cell lines and in the FG/Tag mice more than the single drugs. Overall, our data indicate that low dose 2ME2+Doc combinations may provide a treatment strategy that can improve therapeutic efficacy against AI-PC while reducing toxicity often seen in patients treated with Doc.

Drivers of dissolved organic carbon export in a subarctic catchment: Importance of microbial decomposition, sorption-desorption, peatland and lateral flow.

PubMed

Tang, Jing; Yurova, Alla Y; Schurgers, Guy; Miller, Paul A; Olin, Stefan; Smith, Benjamin; Siewert, Matthias B; Olefeldt, David; Pilesjö, Petter; Poska, Anneli

2018-05-01

Tundra soils account for 50% of global stocks of soil organic carbon (SOC), and it is expected that the amplified climate warming in high latitude could cause loss of this SOC through decomposition. Decomposed SOC could become hydrologically accessible, which increase downstream dissolved organic carbon (DOC) export and subsequent carbon release to the atmosphere, constituting a positive feedback to climate warming. However, DOC export is often neglected in ecosystem models. In this paper, we incorporate processes related to DOC production, mineralization, diffusion, sorption-desorption, and leaching into a customized arctic version of the dynamic ecosystem model LPJ-GUESS in order to mechanistically model catchment DOC export, and to link this flux to other ecosystem processes. The extended LPJ-GUESS is compared to observed DOC export at Stordalen catchment in northern Sweden. Vegetation communities include flood-tolerant graminoids (Eriophorum) and Sphagnum moss, birch forest and dwarf shrub communities. The processes, sorption-desorption and microbial decomposition (DOC production and mineralization) are found to contribute most to the variance in DOC export based on a detailed variance-based Sobol sensitivity analysis (SA) at grid cell-level. Catchment-level SA shows that the highest mean DOC exports come from the Eriophorum peatland (fen). A comparison with observations shows that the model captures the seasonality of DOC fluxes. Two catchment simulations, one without water lateral routing and one without peatland processes, were compared with the catchment simulations with all processes. The comparison showed that the current implementation of catchment lateral flow and peatland processes in LPJ-GUESS are essential to capture catchment-level DOC dynamics and indicate the model is at an appropriate level of complexity to represent the main mechanism of DOC dynamics in soils. The extended model provides a new tool to investigate potential interactions among climate change, vegetation dynamics, soil hydrology and DOC dynamics at both stand-alone to catchment scales. Copyright © 2017 Elsevier B.V. All rights reserved.

Assessing contribution of DOC from sediments to a drinking-water reservoir using optical profiling

USGS Publications Warehouse

Downing, Bryan D.; Bergamaschi, Brian A.; Evans, David G.; Boss, Emmanuel

2008-01-01

Understanding the sources of dissolved organic carbon (DOC) in drinking-water reservoirs is an important management issue because DOC may form disinfection by-products, interfere with disinfection, or increase treatment costs. DOC may be derived from a host of sources-algal production of DOC in the reservoir, marginal production of DOC from mucks and vascular plants at the margins, and sediments in the reservoir. The purpose of this study was to assess if release of DOC from reservoir sediments containing ferric chloride coagulant was a significant source of DOC to the reservoir. We examined the source-specific contributions of DOC using a profiling system to measure the in situ distribution of optical properties of absorption and fluorescence at various locations in the reservoir. Vertical optical profiles were coupled with discrete water samples measured in the laboratory for DOC concentration and optical properties: absorption spectra and excitation emission matrix spectra (EEMs). Modeling the in situ optical data permitted estimation of the bulk DOC profile in the reservoir as well as separation into source-specific contributions. Analysis of the source-specific profiles and their associated optical characteristics indicated that the sedimentary source of DOC to the reservoir is significant and that this DOC is labile in the reservoir. We conclude that optical profiling is a useful technique for understanding complex biogeochemical processes in a reservoir.

Rare Earth Element Concentrations and Fractionation Patterns Along Groundwater Flow Paths in Two Different Aquifer Types (i.e., Sand vs. Carbonate)

NASA Astrophysics Data System (ADS)

Johannesson, K. H.; Tang, J.

2003-12-01

Groundwater samples were collected in two different types of aquifer (i.e., Carrizo Sand Aquifer, Texas and Upper Floridan carbonate Aquifer, west-central Florida) to study the concentrations, fractionation, and speciation of rare earth elements (REE) along groundwater flow paths in each aquifer. Major solutes and dissolved organic carbon (DOC) were also measured in these groundwaters. The Carrizo Sand aquifer was sampled in October 2002 and June 2003, whereas, to date, we have only sampled the Floridan once (i.e., June 2003). The data reveal no significant seasonal differences in major solute and REE concentrations for the Carrizo. In Carrizo sand aquifer, groundwaters from relatively shallow wells (i.e., less than 167 m) in the recharge zone are chiefly Ca-Na-HCO3-Cl type waters. With flow down-gradient the groundwaters shift composition to the Na-HCO3 waters. pH and alkalinity initially decrease with flow away from the recharge zone before increasing again down-gradient. DOC is generally low (0.65 mg/L) along the flow path. REE concentrations are highest in groundwaters from the recharge zone (Nd 40.5 pmol/kg), and decrease substantially with flow down-gradient reaching relatively low and stable values (Nd 4.1-8.6 pmol/kg) roughly 10 km from the recharge zone. Generally, Carrizo groundwaters exhibit HREE-enriched shale-normalized patterns. The HREE enrichments are especially strong for waters from the recharge zone [(Yb/Nd)SN =1.7-5.6], whereas down-gradient (deep) groundwaters have flatter patterns [(Yb/Nd)SN =0.7-2.5]. All groundwaters have slightly positive Eu anomalies (Eu/Eu* 0.09-0.14) and negative Ce anomalies (Ce/Ce* -0.85 - -0.07). In the Upper Floridan Aquifer, Ca, Mg, SO4, and Cl concentrations generally increase along groundwater flow path, whereas pH and alkalinity generally decrease. DOC is higher (0.64 - 2.29 mg/L) than in the Carrizo and initially increases along the flow path and then decreases down-gradient. LREE (Nd) concentrations generally increase along groundwater flow path, however, MREE (Gd) exhibit little change and HREE (Yb) concentrations tend to decreases along the flow path. Floridan groundwaters have HREE enriched shale-normalized patterns, although (Yb/Nd)SN values decrease along groundwater flow path. Thus, REE patterns of Floridan groundwaters tend to flatten with flow down-gradient. All groundwaters show positive Eu anomalies (0.06 - 0.17) and negative Ce anomalies (-0.12 - -0.63).

Modeling rates of DOC degradation using DOM composition and hydroclimatic variables

NASA Astrophysics Data System (ADS)

Moody, C. S.; Worrall, F.

2017-05-01

The fluvial fluxes of dissolved organic carbon (DOC) from peatlands form an important part of that ecosystem's carbon cycle, contributing approximately 35% of the overall peatland carbon budget. The in-stream processes acting on the DOC, such as photodegradation and biodegradation, can lead to DOC loss and thus contribute CO2 to the atmosphere. The aim of this study was to understand what controls the rates of DOC degradation. Water samples from a headwater, peat-covered catchment, were collected over a 23 month period and analyzed for the DOC degradation rate and dissolved organic matter (DOM) composition in the context of hydroclimatic monitoring. Measures of DOM composition included 13C solid-state nuclear magnetic resonance spectroscopy, bomb calorimetry, and elemental analysis. Regression analysis showed that there was a significant role for the composition of the DOM in controlling degradation with degradation rates significantly increasing with the proportion of aldehyde and carboxylic acid functional groups but decreasing with the proportion of N-alkyl functional groups. The highest rates of DOC degradation occurred when aldehyde functionality was at its greatest and this occurred on the recession limb of storm hydrographs. Including this knowledge into models of fluvial carbon fate for an 818 km2 catchment gave an annual average DOC removal rate of 67% and 50% for total organic carbon, slightly lower than previously predicted. The compositional controls suggest that DOM is primarily being used as a ready energy source to the aquatic ecosystem rather than as a nutrient source.

Export of Dissolved Lignin from Coastal Wetlands to the Louisiana Shelf

NASA Astrophysics Data System (ADS)

Bianchi, T. S.; Dimarco, S. F.; Smith, R. W.; Schreiner, K. M.

2008-12-01

Here we report on spatial and temporal changes in the concentration and composition of dissolved lignin- phenols in surface and bottom waters off the Louisiana coast (USA). Samples were collected at 7 stations on 2 cruises (April, and July, 2008) along a transect that spanned from inside Terrebonne Bay, Louisiana (12 m water depth) to the outer-most station on the inner Louisiana shelf (21 m water depth). The highest average concentration of dissolved organic carbon (DOC) and dissolved lignin, during both cruises, occurred at the interface between Terrebonne Bay and the inner shelf. Average DOC and dissolved lignin concentrations were significantly higher in April than in July across most stations. Based on hydrologic data, these higher concentrations clearly reflect a combined mixing of DOM from plume waters to the west and local marsh inputs. The cinnamyl/vanillyl (C/V) and syringyl/vanillyl (S/V) ratios indicated that the predominant source of lignin was from non-woody angiosperms - likely the dominant species of wetland plants Spartina alterniflora and S. patens (Spartina spp.) that border the entire bay. The high vanillic acid to vanillin (Ad/Al)v ratios for all stations were typical of that found near estuarine boundaries, where biologically- and photochemically-mediated lignin decay processes are important. This preliminary data indicates that wetlands provide another source of dissolved organic matter (DOM) to the Louisiana shelf that likely contributes to microbial food resources and hence hypoxia, especially in the context of the instability and extensive erosion of these marshes over the past ca. 50 years. This has important implications for the current management plan to reduce hypoxia in the GOM, particularly in those regions that extend west of the nutrient-rich highly productive near-field zones of Atchafalaya-Mississippi river plumes.

Progress in the Development of Direct Osmotic Concentration Wastewater Recovery Process for Advanced Life Support Systems

NASA Technical Reports Server (NTRS)

Cath, Tzahi Y.; Adams, Dean V.; Childress, Amy; Gormly, Sherwin; Flynn, Michael

2005-01-01

Direct osmotic concentration (DOC) has been identified as a high potential technology for recycling of wastewater to drinking water in advanced life support (ALS) systems. As a result the DOC process has been selected for a NASA Rapid Technology Development Team (RTDT) effort. The existing prototype system has been developed to a Technology Readiness Level (TRL) 3. The current project focuses on advancing the development of this technology from TRL 3 to TRL 6 (appropriate for human rated testing). A new prototype of a DOC system is been designed and fabricated that addresses the deficiencies encountered during the testing of the original system and allowing the new prototype to achieve TRL 6. Background information is provided about the technologies investigated and their capabilities, results from preliminary tests, and the milestones plan and activities for the RTDT program intended to develop a second generation prototype of the DOC system.

Carbon speciation and surface tension of fog

USGS Publications Warehouse

Capel, P.D.; Gunde, R.; Zurcher, F.; Giger, W.

1990-01-01

The speciation of carbon (dissolved/particulate, organic/inorganic) and surface tension of a number of radiation fogs from the urban area of Zurich, Switzerland, were measured. The carbon species were dominated by "dissolved" organic carbon (DOC; i.e., the fraction that passes through a filter), which was typically present at levels of 40-200 mg/L. Less than 10% of the DOC was identified as specific individual organic compounds. Particulate organic carbon (POC) accounted for 26-41% of the mass of the particles, but usually less than 10% of the total organic carbon mass. Inorganic carbon species were relatively minor. The surface tensions of all the measured samples were less than pure water and were correlated with their DOC concentrations. The combination of high DOC and POC and low surface tension suggests a mechanism for the concentration of hydrophobic organic contaminants in the fog droplet, which have been observed by numerous investigators. ?? 1990 American Chemical Society.

Experimental whole-lake dissolved organic carbon increase alters fish diet and density but not growth or productivity

USGS Publications Warehouse

Koizumi, Shuntaro; Craig, Nicola; Zwart, Jacob A.; Kelly, Patrick T.; Ziegler, Jacob P.; Weidel, Brian C.; Jones, Stuart E.; Solomon, Christopher T.

2018-01-01

Negative relationships between dissolved organic carbon (DOC) concentration and fish productivity have been reported from correlative studies across lakes, but to date there have not been experimental tests of these relationships. We increased the DOC concentration in a lake by 3.4 mg L-1, using a before-after control-impact (BACI) design, to quantify the effects on the productivity and population structure of Largemouth Bass (Micropterus salmoides). Greater DOC reduced the volume of the epilimnion, the preferred habitat of Largemouth Bass, resulting in increased bass density. The likelihood that adult bass had empty diets decreased despite this increase in bass density; diet composition also changed. There was no apparent change in bass growth or condition. Overall, there was no net change in Largemouth Bass productivity. However, changes in YOY and juvenile recruitment and feeding success suggest the possibility that future effects could occur. Our results are the first to examine the effects of an increase in DOC on fish productivity through a five-year temporal lens, which demonstrates that the relationship between DOC and fish productivity is multi-dimensional and complex.

Changes in metal mobility associated with bark beetle-induced tree mortality.

PubMed

Mikkelson, Kristin M; Bearup, Lindsay A; Navarre-Sitchler, Alexis K; McCray, John E; Sharp, Jonathan O

2014-05-01

Recent large-scale beetle infestations have caused extensive mortality to conifer forests resulting in alterations to dissolved organic carbon (DOC) cycling, which in turn can impact metal mobility through complexation. This study analyzed soil-water samples beneath impacted trees in concert with laboratory flow-through soil column experiments to explore possible impacts of the bark beetle infestation on metal release and transport. The columns mimicked field conditions by introducing pine needle leachate and artificial rainwater through duplicate homogenized soil columns and measuring effluent metal (focusing on Al, Cu, and Zn) and DOC concentrations. All three metals were consistently found in higher concentrations in the effluent of columns receiving pine needle leachate. In both the field and laboratory, aluminum mobility was largely correlated with the hydrophobic fraction of the DOC, while copper had the largest correlation with total DOC concentrations. Geochemical speciation modeling supported the presence of DOC-metal complexes in column experiments. Copper soil water concentrations in field samples supported laboratory column results, as they were almost twice as high under grey phase trees than under red phase trees further signifying the importance of needle drop. Pine needle leachate contained high concentrations of Zn (0.1 mg l(-1)), which led to high effluent zinc concentrations and sorption of zinc to the soil matrix representing a future potential source for release. In support, field soil-water samples underneath beetle-impacted trees where the needles had recently fallen contained approximately 50% more zinc as samples from under beetle-impacted trees that still held their needles. The high concentrations of carbon in the pine needle leachate also led to increased sorption in the soil matrix creating the potential for subsequent carbon release. While unclear if manifested in adjacent surface waters, these results demonstrate an increased potential for Zn, Cu, and Al mobility, along with increased deposition of metals and carbon beneath beetle-impacted trees.

The role of hydrologic regimes on dissolved organic carbon composition in an agricultural watershed

NASA Astrophysics Data System (ADS)

Hernes, Peter J.; Spencer, Robert G. M.; Dyda, Rachael Y.; Pellerin, Brian A.; Bachand, Philip A. M.; Bergamaschi, Brian A.

2008-11-01

Willow Slough, a seasonally irrigated agricultural watershed in the Sacramento River valley, California, was sampled weekly in 2006 in order to investigate seasonal concentrations and compositions of dissolved organic carbon (DOC). Average DOC concentrations nearly doubled from winter baseflow (2.75 mg L -1) to summer irrigation (5.14 mg L -1), while a concomitant increase in carbon-normalized vanillyl phenols (0.11 mg 100 mg OC -1 increasing to 0.31 mg 100 mg OC -1, on average) indicates that this additional carbon is likely vascular plant-derived. A strong linear relationship between lignin concentration and total suspended sediments ( r2 = 0.79) demonstrates that agricultural management practices that mobilize sediments will likely have a direct and significant impact on DOC composition. The original source of vascular plant-derived DOC to Willow Slough appears to be the same throughout the year as evidenced by similar syringyl to vanillyl and cinnamyl to vanillyl ratios. However, differing diagenetic pathways during winter baseflow as compared to the rest of the year are evident in acid to aldehyde ratios of both vanillyl and syringyl phenols. The chromophoric dissolved organic matter (CDOM) absorption coefficient at 350 nm showed a strong correlation with lignin concentration ( r2 = 0.83). Other CDOM measurements related to aromaticity and molecular weight also showed correlations with carbon-normalized yields (e.g. specific UV absorbance at 254 nm ( r2 = 0.57) and spectral slope ( r2 = 0.54)). Our overall findings suggest that irrigated agricultural watersheds like Willow Slough can potentially have a significant impact on mainstem DOC concentration and composition when scaled to the entire watershed of the main tributary.

Temporal trends in organic carbon content in the main Swiss rivers, 1974-2010.

PubMed

Rodríguez-Murillo, J C; Zobrist, J; Filella, M

2015-01-01

Increases in dissolved organic carbon (DOC) concentrations have often been reported in rivers and lakes of the Northern Hemisphere over the last few decades. High-quality organic carbon (OC) concentration data have been used to study the change in DOC and total (TOC) organic carbon concentrations in the main rivers of Switzerland (Rhône, Rhine, Thur and Aar) between 1974 and 2010. These rivers are characterized by high discharge regimes (due to their Alpine origin) and by running in populated areas. Small long term trends (a general statistically significant decrease in TOC and a less clear increase in DOC concentrations), on the order of 1% of mean OC concentration per year, have been observed. An upward trend before 1999 reversed direction to a more marked downward trend from 1999 to 2010. Of the potential causes of OC temporal variation analysed (water temperature, dissolved reactive phosphorus and river discharge), only discharge explains a significant, albeit still small, part of TOC variability (8-31%), while accounting for barely 2.5% of DOC variability. Estimated anthropogenic TOC and DOC loads (treated sewage) to the rivers could account for a maximum of 4-20% of the temporal trends. Such low predictability is a good example of the limitations faced when studying causality and drivers behind small variations in complex systems. River export of OC from Switzerland has decreased significantly over the period. Since about 5.5% of estimated NEP of Switzerland is exported by the rivers, riverine OC fluxes should be taken into account in a detailed carbon budget of the country. Copyright © 2014 Elsevier B.V. All rights reserved.

Influence of Concentration and Salinity on the Biodegradability of Organic Additives in Hydraulic Fracturing Fluid

NASA Astrophysics Data System (ADS)

Mouser, P. J.; Kekacs, D.

2014-12-01

One of the risks associated with the use of hydraulic fracturing technologies for energy development is the potential release of hydraulic fracturing-related fluids into surface waters or shallow aquifers. Many of the organic additives used in hydraulic fracturing fluids are individually biodegradable, but little is know on how they will attenuate within a complex organic fluid in the natural environment. We developed a synthetic hydraulic fracturing fluid based on disclosed recipes used by Marcellus shale operators to evaluate the biodegradation potential of organic additives across a concentration (25 to 200 mg/L DOC) and salinity gradient (0 to 60 g/L) similar to Marcellus shale injected fluids. In aerobic aqueous solutions, microorganisms removed 91% of bulk DOC from low SFF solutions and 57% DOC in solutions having field-used SFF concentrations within 7 days. Under high SFF concentrations, salinity in excess of 20 g/L inhibited organic compound biodegradation for several weeks, after which time the majority (57% to 75%) of DOC remained in solution. After SFF amendment, the initially biodiverse lake or sludge microbial communities were quickly dominated (>79%) by Pseudomonas spp. Approximately 20% of added carbon was converted to biomass while the remainder was respired to CO2 or other metabolites. Two alcohols, isopropanol and octanol, together accounted for 2-4% of the initial DOC, with both compounds decreasing to below detection limits within 7 days. Alcohol degradation was associated with an increase in acetone at mg/L concentrations. These data help to constrain the biodegradation potential of organic additives in hydraulic fracturing fluids and guide our understanding of the microbial communities that may contribute to attenuation in surface waters.

The role of hydrologic regimes on dissolved organic carbon composition in an agricultural watershed

USGS Publications Warehouse

Hernes, P.J.; Spencer, R.G.M.; Dyda, R.Y.; Pellerin, B.A.; Bachand, P.A.M.; Bergamaschi, B.A.

2008-01-01

Willow Slough, a seasonally irrigated agricultural watershed in the Sacramento River valley, California, was sampled weekly in 2006 in order to investigate seasonal concentrations and compositions of dissolved organic carbon (DOC). Average DOC concentrations nearly doubled from winter baseflow (2.75 mg L-1) to summer irrigation (5.14 mg L-1), while a concomitant increase in carbon-normalized vanillyl phenols (0.11 mg 100 mg OC-1 increasing to 0.31 mg 100 mg OC-1, on average) indicates that this additional carbon is likely vascular plant-derived. A strong linear relationship between lignin concentration and total suspended sediments (r2 = 0.79) demonstrates that agricultural management practices that mobilize sediments will likely have a direct and significant impact on DOC composition. The original source of vascular plant-derived DOC to Willow Slough appears to be the same throughout the year as evidenced by similar syringyl to vanillyl and cinnamyl to vanillyl ratios. However, differing diagenetic pathways during winter baseflow as compared to the rest of the year are evident in acid to aldehyde ratios of both vanillyl and syringyl phenols. The chromophoric dissolved organic matter (CDOM) absorption coefficient at 350 nm showed a strong correlation with lignin concentration (r2 = 0.83). Other CDOM measurements related to aromaticity and molecular weight also showed correlations with carbon-normalized yields (e.g. specific UV absorbance at 254 nm (r2 = 0.57) and spectral slope (r2 = 0.54)). Our overall findings suggest that irrigated agricultural watersheds like Willow Slough can potentially have a significant impact on mainstem DOC concentration and composition when scaled to the entire watershed of the main tributary. ?? 2008 Elsevier Ltd.

Concentrations, loads, and yields of organic carbon in streams of agricultural watersheds

USGS Publications Warehouse

Kronholm, Scott; Capel, Paul

2012-01-01

Carbon is cycled to and from large reservoirs in the atmosphere, on land, and in the ocean. Movement of organic carbon from the terrestrial reservoir to the ocean plays an important role in the global cycling of carbon. The transition from natural to agricultural vegetation can change the storage and movement of organic carbon in and from a watershed. Samples were collected from 13 streams located in hydrologically and agriculturally diverse watersheds, to better understand the variability in the concentrations and loads of dissolved organic carbon (DOC) and particulate organic carbon (POC) in the streams, and the variability in watershed yields. The overall annual median concentrations of DOC and POC were 4.9 (range: 2.1–6.8) and 1.1 (range: 0.4–3.8) mg C L−1, respectively. The mean DOC watershed yield (± SE) was 25 ± 6.8 kg C ha−1 yr−1. The yields of DOC from these agricultural watersheds were not substantially different than the DOC yield from naturally vegetated watersheds in equivalent biomes, but were at the low end of the range for most biomes. Total organic carbon (DOC + POC) annually exported from the agricultural watersheds was found to average 0.03% of the organic carbon that is contained in the labile plant matter and top 1 m of soil in the watershed. Since the total organic carbon exported from agricultural watersheds is a relatively small portion of the sequestered carbon within the watershed, there is the great potential to store additional carbon in plants and soils of the watershed, offsetting some anthropogenic CO2 emissions.

Freshwater DOM quantity and quality from a two-component model of UV absorbance

USGS Publications Warehouse

Carter, Heather T.; Tipping, Edward; Koprivnjak, Jean-Francois; Miller, Matthew P.; Cookson, Brenda; Hamilton-Taylor, John

2012-01-01

We present a model that considers UV-absorbing dissolved organic matter (DOM) to consist of two components (A and B), each with a distinct and constant spectrum. Component A absorbs UV light strongly, and is therefore presumed to possess aromatic chromophores and hydrophobic character, whereas B absorbs weakly and can be assumed hydrophilic. We parameterised the model with dissolved organic carbon concentrations [DOC] and corresponding UV spectra for c. 1700 filtered surface water samples from North America and the United Kingdom, by optimising extinction coefficients for A and B, together with a small constant concentration of non-absorbing DOM (0.80 mg DOC L-1). Good unbiased predictions of [DOC] from absorbance data at 270 and 350 nm were obtained (r2 = 0.98), the sum of squared residuals in [DOC] being reduced by 66% compared to a regression model fitted to absorbance at 270 nm alone. The parameterised model can use measured optical absorbance values at any pair of suitable wavelengths to calculate both [DOC] and the relative amounts of A and B in a water sample, i.e. measures of quantity and quality. Blind prediction of [DOC] was satisfactory for 9 of 11 independent data sets (181 of 213 individual samples).

Carbon isotope analysis of dissolved organic carbon in fresh and saline (NaCl) water via continuous flow cavity ring-down spectroscopy following wet chemical oxidation

USGS Publications Warehouse

Conaway, Christopher; Thomas, Randal B.; Saad, Nabil; Thordsen, James J.; Kharaka, Yousif K.

2015-01-01

This work examines the performance and limitations of a wet chemical oxidation carbon analyser interfaced with a cavity ring-down spectrometer (WCO-CRDS) in a continuous flow (CF) configuration for measuring δ13C of dissolved organic carbon (δ13C-DOC) in natural water samples. Low-chloride matrix (<5 g Cl/L) DOC solutions were analysed with as little as 2.5 mg C/L in a 9 mL aliquot with a precision of 0.5 ‰. In high-chloride matrix (10–100 g Cl/L) DOC solutions, bias towards lighter δ13C-DOC was observed because of incomplete oxidation despite using high-concentration oxidant, extended reaction time, or post-wet chemical oxidation gas-phase combustion. However, through a combination of dilution, chloride removal, and increasing the oxidant:sample ratio, high-salinity samples with sufficient DOC (>22.5 µg C/aliquot) may be analysed. The WCO-CRDS approach requires more total carbon (µg C/aliquot) than conventional CF-isotope ratio mass spectrometer, but is nonetheless applicable to a wide range of DOC concentration and water types, including brackish water, produced water, and basinal brines.

Dissolved carbon and nitrogen dynamics in paddy fields under different water management practices and implications on green-house gas emissions

NASA Astrophysics Data System (ADS)

Miniotti, Eleonora; Said-Pullicino, Daniel; Bertora, Chiara; Pelissetti, Simone; Sacco, Dario; Grignani, Carlo; Lerda, Cristina; Romani, Marco; Celi, Luisella

2013-04-01

The alternation of oxidizing and reducing conditions in paddy soils results in considerable complexity in the biogeochemical cycling of elements and their interactions, influencing important soil processes. Water management practices may play an important role in controlling the loss of nutrients from rice paddies to surface and subsurface waters, as well as soil organic matter (SOM) stabilization and the emission of green-house gases (GHG) such as methane and nitrous oxide. The aim of this study was therefore to evaluate the interaction between changes in soil redox conditions and element cycling in temperate paddy soils as a function of different water management practices. The research was carried out within an experimental platform (1.2 ha) located at the Rice Research Center of Ente Nazionale Risi (Castello d'Agogna, PV, NW Italy) where three water management practices are being compared with two plots for each treatment. These included (i) rice cultivation under traditional submerged conditions (FLD); (ii) seeding under dry soil conditions and flooding delayed by about 40 days (DRY); (iii) seeding under dry soil conditions and rotational irrigation (IRR). Surface and subsurface (25, 50 and 75 cm) water samples were collected at regular intervals over the cropping season from V-notch weirs and porous ceramic suction cups installed in each plot, and subsequently analyzed for DOC, SUVA, Fe(II), ammonium and nitrate-N. Moreover, methane and nitrous oxide fluxes were measured in situ by the closed-chamber technique. DOC concentrations in soil solutions were generally higher in FLD and DRY treatments with respect to IRR throughout the cropping season. Higher DOC contents after field flooding in FLD and DRY treatments also corresponded with greater concentrations of reduced Fe, higher SUVA values, lower Eh values and higher pH values, suggesting that desorption of more aromatic, mineral-associated SOM could be responsible for the observed increase in DOC. These trends were not observed in the IRR treatment. The differences in DOC contents and in Eh trend between treatments could possibly explain the increasing trend in cumulative methane emissions in the order IRR<

High-frequency DOC and nitrate measurements provide new insights into their export and their relationships to rainfall-runoff processes

NASA Astrophysics Data System (ADS)

Schwab, Michael; Klaus, Julian; Pfister, Laurent; Weiler, Markus

2015-04-01

Over the past decades, stream sampling protocols for environmental tracers were often limited by logistical and technological constraints. Long-term sampling programs would typically rely on weekly sampling campaigns, while high-frequency sampling would remain restricted to a few days or hours at best. We stipulate that the currently predominant sampling protocols are too coarse to capture and understand the full amplitude of rainfall-runoff processes and its relation to water quality fluctuations. Weekly sampling protocols are not suited to get insights into the hydrological system during high flow conditions. Likewise, high frequency measurements of a few isolated events do not allow grasping inter-event variability in contributions and processes. Our working hypothesis is based on the potential of a new generation of field-deployable instruments for measuring environmental tracers at high temporal frequencies over an extended period. With this new generation of instruments we expect to gain new insights into rainfall-runoff dynamics, both at intra- and inter-event scales. Here, we present the results of one year of DOC and nitrate measurements with the field deployable UV-Vis spectrometer spectro::lyser (scan Messtechnik GmbH). The instrument measures the absorption spectrum from 220 to 720 nm in situ and at high frequencies and derives DOC and nitrate concentrations. The measurements were carried out at 15 minutes intervals in the Weierbach catchment (0.47 km2) in Luxemburg. This fully forested catchment is characterized by cambisol soils and fractured schist as underlying bedrock. The time series of DOC and nitrate give insights into the high frequency dynamics of stream water. Peaks in DOC concentrations are closely linked to discharge peaks that occur during or right after a rainfall event. Those first discharge peaks can be linked to fast near surface runoff processes and are responsible for a remarkable amount of DOC export. A special characterisation of the Weierbach catchment are the delayed second peaks a few days after the rainfall event. Nitrate concentrations are following this second peak. We assume that this delayed response is going back to subsurface or upper groundwater flows, with nitrate enriched water. On an inter-event scale during low flow / base flow conditions, we observe interesting diurnal patterns of both DOC and nitrate concentrations. Overall, the long-term high-frequency measurements of DOC and nitrate provide us the opportunity to separate different rainfall-runoff processes and link the amount of DOC and nitrate export to them to quantify the overall relevance of the different processes.

Dissolved black carbon in grassland streams: is there an effect of recent fire history?

PubMed

Ding, Yan; Yamashita, Youhei; Dodds, Walter K; Jaffé, Rudolf

2013-03-01

While the existence of black carbon as part of dissolved organic matter (DOM) has been confirmed, quantitative determinations of dissolved black carbon (DBC) in freshwater ecosystem and information on factors controlling its concentration are scarce. In this study, stream surface water samples from a series of watersheds subject to different burn frequencies in Konza Prairie (Kansas, USA) were collected in order to determine if recent fire history has a noticeable effect on DBC concentration. The DBC levels detected ranged from 0.04 to 0.11 mg L(-1), accounting for ca. 3.32±0.51% of dissolved organic carbon (DOC). No correlation was found between DBC concentration and neither fire frequency nor time since last burn. We suggest that limited DBC flux is related to high burning efficiency, possibly greater export during periods of high discharge and/or the continuous export of DBC over long time scales. A linear correlation between DOC and DBC concentrations was observed, suggesting the export mechanisms determining DOC and DBC concentrations are likely coupled. The potential influence of fire history was less than the influence of other factors controlling the DOC and DBC dynamics in this ecosystem. Assuming similar conditions and processes apply in grasslands elsewhere, extrapolation to a global scale would suggest a global grasslands flux of DBC on the order of 0.14 Mt carbon year(-1). Copyright © 2012 Elsevier Ltd. All rights reserved.

Dissolved organic carbon content and characteristics in relation to carbon dioxide partial pressure across Poyang Lake wetlands and adjacent aquatic systems in the Changjiang basin.

PubMed

Wang, Huaxin; Jiao, Ruyuan; Wang, Fang; Zhang, Lu; Yan, Weijin

2016-12-01

Dissolved organic carbon (DOC) plays diverse roles in carbon biogeochemical cycles. Here, we explored the link between DOC and pCO 2 using high-performance size-exclusion chromatography (HPSEC) with UV 254 detection and excitation emission matrix (EEM) fluorescence spectroscopy to determine the molecular weight distribution (MW) and the spectral characteristics of DOC, respectively. The relationship between DOC and pCO 2 was investigated in the Poyang Lake wetlands and their adjacent aquatic systems. The results indicated significant spatial variation in the DOC concentrations, MW distributions, and pCO 2 . The DOC concentration was higher in the wetlands than in the rivers and lakes. pCO 2 was high in wetlands in which the dominant vegetation was Phragmites australis, whereas it was low in wetlands in which Carex tristachya was the dominant species. DOC was divided into five fractions according to MW, as follows: super-low MW (SLMW, <1 kDa); low MW (LMW, 1-2.5 kDa); intermediate MW (IMW, 2.5-3.5 kDa); high MW (HMW, 3.5-6 kDa); and super-high MW (SMW, > 40 kDa). Rivers contained high proportions of HMW and extremely low amounts of SLMW, whereas wetlands had relatively high proportions of SLMW. The proportion of SMW (SMW p ) was particularly high in wetlands. We found that pCO 2 significantly positively correlated with the proportion of IMW, and significantly negatively correlated with SMW p . These data improve our understanding of the MW of bioavailable DOC and its conversion to CO 2 . The present results demonstrate that both the content and characteristics of DOC significantly affect pCO 2 . pCO 2 and DOC must be studied further to help understanding the role of the wetland on the regional CO 2 budget. Copyright © 2016 Elsevier Ltd. All rights reserved.

Carbon and nitrogen stoichiometry across stream ecosystems

NASA Astrophysics Data System (ADS)

Wymore, A.; Kaushal, S.; McDowell, W. H.; Kortelainen, P.; Bernhardt, E. S.; Johnes, P.; Dodds, W. K.; Johnson, S.; Brookshire, J.; Spencer, R.; Rodriguez-Cardona, B.; Helton, A. M.; Barnes, R.; Argerich, A.; Haq, S.; Sullivan, P. L.; López-Lloreda, C.; Coble, A. A.; Daley, M.

2017-12-01

Anthropogenic activities are altering carbon and nitrogen concentrations in surface waters globally. The stoichiometry of carbon and nitrogen regulates important watershed biogeochemical cycles; however, controls on carbon and nitrogen ratios in aquatic environments are poorly understood. Here we use a multi-biome and global dataset (tropics to Arctic) of stream water chemistry to assess relationships between dissolved organic carbon (DOC) and nitrate, ammonium and dissolved organic nitrogen (DON), providing a new conceptual framework to consider interactions between DOC and the multiple forms of dissolved nitrogen. We found that across streams the total dissolved nitrogen (TDN) pool is comprised of very little ammonium and as DOC concentrations increase the TDN pool shifts from nitrate to DON dominated. This suggests that in high DOC systems, DON serves as the primary source of nitrogen. At the global scale, DOC and DON are positively correlated (r2 = 0.67) and the average C: N ratio of dissolved organic matter (molar ratio of DOC: DON) across our data set is approximately 31. At the biome and smaller regional scale the relationship between DOC and DON is highly variable (r2 = 0.07 - 0.56) with the strongest relationships found in streams draining the mixed temperate forests of the northeastern United States. DOC: DON relationships also display spatial and temporal variability including latitudinal and seasonal trends, and interactions with land-use. DOC: DON ratios correlated positively with gradients of energy versus nutrient limitation pointing to the ecological role (energy source versus nutrient source) that DON plays with stream ecosystems. Contrary to previous findings we found consistently weak relationships between DON and nitrate which may reflect DON's duality as an energy or nutrient source. Collectively these analyses demonstrate how gradients of DOC drive compositional changes in the TDN pool and reveal a high degree of variability in the C: N ratio (3-100) of stream water dissolved organic matter.

Enhanced DOC removal using anion and cation ion exchange resins.

PubMed

Arias-Paic, Miguel; Cawley, Kaelin M; Byg, Steve; Rosario-Ortiz, Fernando L

2016-01-01

Hardness and DOC removal in a single ion exchange unit operation allows for less infrastructure, is advantageous for process operation and depending on the water source, could enhance anion exchange resin removal of dissolved organic carbon (DOC). Simultaneous application of cationic (Plus) and anionic (MIEX) ion exchange resin in a single contact vessel was tested at pilot and bench scales, under multiple regeneration cycles. Hardness removal correlated with theoretical predictions; where measured hardness was between 88 and 98% of the predicted value. Comparing bench scale DOC removal of solely treating water with MIEX compared to Plus and MIEX treated water showed an enhanced DOC removal, where removal was increased from 0.5 to 1.25 mg/L for the simultaneous resin application compared to solely applying MIEX resin. A full scale MIEX treatment plant (14.5 MGD) reduced raw water DOC from 13.7 mg/L to 4.90 mg/L in the treated effluent at a bed volume (BV) treatment rate of 800, where a parallel operation of a simultaneous MIEX and Plus resin pilot (10 gpm) measured effluent DOC concentrations of no greater than 3.4 mg/L, even at bed volumes of treatment 37.5% greater than the full scale plant. MIEX effluent compared to simultaneous Plus and MIEX effluent resulted in differences in fluorescence intensity that correlated to decreases in DOC concentration. The simultaneous treatment of Plus and MIEX resin produced water with predominantly microbial character, indicating the enhanced DOC removal was principally due to increased removal of terrestrially derived organic matter. The addition of Plus resin to a process train with MIEX resin allows for one treatment process to remove both DOC and hardness, where a single brine waste stream can be sent to sewer at a full-scale plant, completely removing lime chemical addition and sludge waste disposal for precipitative softening processes. Published by Elsevier Ltd.

Effects of dissolved organic carbon on the toxicity of copper to the developing embryos of the Pacific oyster (Crassostrea gigas).

PubMed

Brooks, Steven J; Bolam, Thi; Tolhurst, Laura; Bassett, Janice; La Roche, Jay; Waldock, Mike; Barry, Jon; Thomas, Kevin V

2007-08-01

The effects of humic acid (HA) on copper speciation and its subsequent toxicity to the sensitive early life stages of the Pacific oyster (Crassostrea gigas) are presented. Differential pulse anodic stripping voltammetry with a hanging mercury drop electrode was used to measure the copper species as labile copper (LCu; free ion and inorganic copper complexes) and total copper (TCu) with respect to increasing HA concentration. The TCu and LCu 50% effect concentrations (EC50s) in the absence of HA were 20.77 microg/L (95% confidence interval [CI], 24.02-19.97 microg/L) and 8.05 microg/L (95% CI, 9.6-5.92 microg/L) respectively. A corrected dissolved organic carbon (DOC) concentration (HA only) of 1.02 mg/L was required to significantly increase the TCu EC50 to approximately 41.09 microg/L (95% CI, 44.27-37.52 microg/L; p < 0.05), almost doubling that recorded when DOC (as HA) was absent from the test media. In contrast, the LCu EC50 was unaffected by changes in DOC concentration and was stable throughout the corrected DOC concentration range. The absence of change in the LCu EC50, despite increased HA concentration, suggests that the LCu fraction, not TCu, was responsible for the observed toxicity to the oyster embryo. This corresponds with the current understanding of copper toxicity and supports the free-ion activity model for copper toxicity.

Impact of Wet Deposition of Black Carbon on Particle Dynamics in Surface Waters of Halong Bay, North Vietnam

NASA Astrophysics Data System (ADS)

Mari, X.; Guinot, B. P.; Thuoc, C. V.; Brune, J.; Lefebvre, J. P.; Raimbault, P.; Niggemann, J.; Dittmar, T.

2016-02-01

Black Carbon (BC) is an aerosol emitted during biomass burning and fossil fuel combustion. The atmospheric lifetime of Black Carbon (BC) ranges from a few days in rainy climates up to one month in dry regions, and on a global scale wet deposition of atmospheric BC accounts for about 80% of the BC input to the ocean. The rain-mediated input of BC to the ocean was studied in a coastal site located in a regional hotspot of atmospheric BC concentration, North Vietnam. We monitored changes in atmospheric and marine BC during a 24-h cycle impacted by a short and heavy rainfall event. During the rainfall event, atmospheric BC concentration decreased by a factor of 8 (i.e. from 5230 to 660 µg BC m-3). This cleaning of the air column was immediately followed by a significant increase (by a factor of 2 to 4) of particulate BC (PBC) and POC concentrations in the surface microlayer (SML) and at 1.5 m depth. In the SML, this event was also followed by a significant increase of DOC and dissolved BC (DBC) concentrations. Interestingly, the concentration of DOC decreased by >10% after the rainfall at 1.5 m depth, suggesting an adsorption of DOC onto sinking PBC. Concomitantly with the increase in particulate BC, nutrient concentrations increased by a factor of 2 in the SML, while no change was observed in the underlying water column. After the rainfall, the particle size spectra, measured along the water column with a LISST (Laser In-Situ Scattering and Transmissometry probe), changed in that the concentration of small particles (<5 µm) decreased and the concentration of large particles (>100 µm) increased. This alteration of the particle size spectra was restricted to a thin layer of about 20 cm thickness, probably corresponding to a BC-enriched layer adsorbing DOC and small particles, and stimulating aggregation during sinking from the surface to deeper water layers. The concentrations of POC, DOC, PBC, DBC and nutrients reached pre-rainfall levels 4 hours after the event.

Contributions of humic substances to the dissolved organic carbon pool in wetlands from different climates.

PubMed

Watanabe, Akira; Moroi, Kunio; Sato, Hiromu; Tsutsuki, Kiyoshi; Maie, Nagamitsu; Melling, Lulie; Jaffé, Rudolf

2012-08-01

Wetlands are an important source of DOM. However, the quantity and quality of wetlands' DOM from various climatic regions have not been studied comprehensively. The relationship between the concentrations of DOM (DOC), humic substances (HS) and non-humic substances (NHS) in wetland associated sloughs, streams and rivers, in cool temperate (Hokkaido, Japan), sub-tropical (Florida, USA), and tropical (Sarawak, Malaysia) regions was investigated. The DOC ranged from 1.0 to 15.6 mg CL(-1) in Hokkaido, 6.0-24.4 mg CL(-1) in Florida, and 18.9-75.3 mg CL(-1) in Sarawak, respectively. The relationship between DOC and HS concentrations for the whole sample set was regressed to a primary function with y-intercept of zero (P<0.005) and a slope value of 0.841. A similar correlation was observed between DOC and NHS concentrations, with a smaller slope value of 0.159. However, the correlation coefficient of the latter was much larger when the data was regressed to a logarithmic curve. These observations suggest the presence of a general tendency that the increased DOC in the river waters was mainly due to the increased supply of HS from wetland soils, whereas the rate of the increase in the NHS supply has an upper limit which may be controlled by primary productivity. Copyright © 2012 Elsevier Ltd. All rights reserved.

Wet Removal of Organic and Black Carbon Aerosols

NASA Astrophysics Data System (ADS)

Torres, A.; Bond, T. C.; Lehmann, C.

2012-12-01

Organic carbon (OC) and black carbon (BC) aerosols derived from the combustion of fossil fuels and biomass are significant atmospheric pollutants that alter the Earth's radiation balance and affect human health. Carbonaceous aerosol lifetime and extent of its effects are mainly controlled by its wet removal, especially by rain. Limited work has been done to measure both BC and OC from rain events even though these aerosols are co-emitted and exist together in the atmosphere. The choices of analytical techniques for measuring OC and BC in water are limited, and researchers often employ the same techniques used for measuring atmospheric carbon particles. There is no agreement in the methods employed for monitoring carbon concentration in precipitation. As part of the method development, the Single Particle Soot Photometer (SP2), Thermal-Optical Analysis (TOA), Ultraviolet/Visible (UV/VIS) Spectrophotometer, and the Total Organic Carbon (TOC) Analyzer were evaluated for measuring BC suspended in water, water insoluble OC (WIOC) and dissolved OC (DOC). The study also monitored the concentration of BC, WIOC, and DOC in rainwater collected at Bondville (Illinois) for 18 months. Results indicated that 34% (±3%) of the BC mass was lost in the SP2 analysis, most probably during the nebulization process. Filtration required for TOA also had large losses (>75%) because quartz fiber filters were ineffective for capturing BC particles from water. Addition of NH4H2PO4 as a coagulant improved (>95%) the capture efficiency of the filters. UV/VIS spectrophotometry had good linearity, but the sensitivity for detecting BC particles (±20 μg/L) suspended in water was inadequate. TOC analysis was a robust technique for measuring both DOC and total carbon (BC + OC). The chosen techniques were TOC analysis for DOC, and TOA with an optimized filtration procedure for BC and WIOC. The mean concentrations in rainwater were 8.72 (±9.84) μg/L of BC, 88.97 (±62.64) μg/L of WIOC, and 1,320 (1,380) μg/L of DOC. DOC contributed, mostly with anions, to the ion balance of rain samples. The total carbon concentration (BC+WIOC+DOC) decreased with increasing precipitation volume and directly correlated with the concentrations of SO42-, NO3-, Ca2+, NH4+, Mg2+, and K+ in rainwater.

Storage effects on quantity and composition of dissolved organic carbon and nitrogen of lake water, leaf leachate and peat soil water.

PubMed

Heinz, Marlen; Zak, Dominik

2018-03-01

This study aimed to evaluate the effects of freezing and cold storage at 4 °C on bulk dissolved organic carbon (DOC) and nitrogen (DON) concentration and SEC fractions determined with size exclusion chromatography (SEC), as well as on spectral properties of dissolved organic matter (DOM) analyzed with fluorescence spectroscopy. In order to account for differences in DOM composition and source we analyzed storage effects for three different sample types, including a lake water sample representing freshwater DOM, a leaf litter leachate of Phragmites australis representing a terrestrial, 'fresh' DOM source and peatland porewater samples. According to our findings one week of cold storage can bias DOC and DON determination. Overall, the determination of DOC and DON concentration with SEC analysis for all three sample types were little susceptible to alterations due to freezing. The findings derived for the sampling locations investigated here may not apply for other sampling locations and/or sample types. However, DOC size fractions and DON concentration of formerly frozen samples should be interpreted with caution when sample concentrations are high. Alteration of some optical properties (HIX and SUVA 254 ) due to freezing were evident, and therefore we recommend immediate analysis of samples for spectral analysis. Copyright © 2017 Elsevier Ltd. All rights reserved.

The impact of four decades of annual nitrogen addition on dissolved organic matter in a boreal forest soil

NASA Astrophysics Data System (ADS)

Rappe-George, M. O.; Gärdenäs, A. I.; Kleja, D. B.

2013-03-01

Addition of mineral nitrogen (N) can alter the concentration and quality of dissolved organic matter (DOM) in forest soils. The aim of this study was to assess the effect of long-term mineral N addition on soil solution concentration of dissolved organic carbon (DOC) and dissolved organic nitrogen (DON) in Stråsan experimental forest (Norway spruce) in central Sweden. N was added yearly at two levels of intensity and duration: the N1 treatment represented a lower intensity but a longer duration (43 yr) of N addition than the shorter N2 treatment (24 yr). N additions were terminated in the N2 treatment in 1991. The N treatments began in 1967 when the spruce stands were 9 yr old. Soil solution in the forest floor O, and soil mineral B, horizons were sampled during the growing seasons of 1995 and 2009. Tension and non-tension lysimeters were installed in the O horizon (n = 6), and tension lysimeters were installed in the underlying B horizon (n = 4): soil solution was sampled at two-week intervals. Although tree growth and O horizon carbon (C) and N stock increased in treatments N1 and N2, the concentration of DOC in O horizon leachates was similar in both N treatments and control. This suggests an inhibitory direct effect of N addition on O horizon DOC. Elevated DON and nitrate in O horizon leachates in the ongoing N1 treatment indicated a move towards N saturation. In B horizon leachates, the N1 treatment approximately doubled leachate concentrations of DOC and DON. DON returned to control levels, but DOC remained elevated in B horizon leachates in N2 plots nineteen years after termination of N addition. We propose three possible explanations for the increased DOC in mineral soil: (i) the result of decomposition of a larger amount of root litter, either directly producing DOC or (ii) indirectly via priming of old SOM, and/or (iii) a suppression of extracellular oxidative enzymes.

Required ozone doses for removing pharmaceuticals from wastewater effluents.

PubMed

Antoniou, Maria G; Hey, Gerly; Rodríguez Vega, Sergio; Spiliotopoulou, Aikaterini; Fick, Jerker; Tysklind, Mats; la Cour Jansen, Jes; Andersen, Henrik Rasmus

2013-07-01

The aim of the this study was to investigate the ozone dosage required to remove active pharmaceutical ingredients (APIs) from biologically treated wastewater of varying quality, originated from different raw wastewater and wastewater treatment processes. Secondary effluents from six Swedish wastewater treatment plants (WWTP) were spiked with 42 APIs (nominal concentration μg/L) and treated with different O₃ doses (0.5-12.0 mg/L ozone) in bench-scale experiments. In order to compare the sensitivity of APIs in each matrix, the specific dose of ozone required to achieve reduction by one decade of each investigated API (DDO₃) was determined for each effluent by fitting a first order equation to the remaining concentration of API at each applied ozone dose. Ozone dose requirements were found to vary significantly between effluents depending on their matrix characteristics. The specific ozone dose was then normalized to the dissolved organic carbon (DOC) of each effluent. The DDO₃/DOC ratios were comparable for each API between the effluents. 15 of the 42 investigated APIs could be classified as easily degradable (DDO₃/DOC ≤ 0.7), while 19 were moderately degradable (0.7 < DDO₃/DOC ≤ 1.4), and 8 were recalcitrant towards O₃-treatment (DDO₃/DOC >1.4). Furthermore, we predict that a reasonable estimate of the ozone dose required to remove any of the investigated APIs may be attained by multiplying the experimental average DDO₃/DOC obtained with the actual DOC of any effluent. Copyright © 2013 Elsevier B.V. All rights reserved.

Spatiotemporal characterization of dissolved carbon for inland waters in semi-humid/semi-arid region, China

NASA Astrophysics Data System (ADS)

Song, K. S.; Zang, S. Y.; Zhao, Y.; Li, L.; Du, J.; Zhang, N. N.; Wang, X. D.; Shao, T. T.; Guan, Y.; Liu, L.

2013-10-01

Spatiotemporal variations of dissolved organic carbon (DOC) and inorganic carbon (DIC) in 26 waters across the semi-humid/semi-arid Songnen Plain, China, were examined with data collected during 2008-2011. Fresh (n = 14) and brackish (n = 12) waters were grouped according to electrical conductivity (threshold = 1000 μS cm-1) Significant differences in the average DOC and DIC concentrations were observed between the fresh (5.63 mg L-1, 37.39 mg L-1) and the brackish waters (15.33 mg L-1, 142.93 mg L-1). Colored dissolved organic matter (CDOM) and DOC concentrations were mainly controlled by climatic-hydrologic conditions. The investigation indicated that the outflow conditions in the semi-arid region had condensed effects on the dissolved carbon, resulting in close relationships between salinity vs. DOC (R2 = 0.66), and salinity vs. DIC (R2 = 0.94). An independent data set collected in May 2012 also confirmed this finding (DOC: R2 = 0.79, DIC: R2 = 0.91), highlighting the potential of quantifying DOC and DIC via salinity measurements for waters dispersed in the plain. Indices based on the CDOM absorption spectra (e.g., the DOC-specific CDOM absorption (SUVA254), absorption ratio a250 : a365 (E250 : E365) and the spectral slope ratio (Sr, S275-295/S350-400) were applied to characterize CDOM composition and quality. Our results indicate that high molecular weight CDOM fractions are more abundant in the fresh waters than the brackish waters.

Spatiotemporal characterization of dissolved carbon for inland waters in semi-humid/semiarid region, China

NASA Astrophysics Data System (ADS)

Song, K. S.; Zang, S. Y.; Zhao, Y.; Du, J.; Li, L.; Zhang, N. N.; Wang, X. D.; Shao, T. T.; Guan, Y.; Liu, L.

2013-05-01

Spatiotemporal variations of dissolved organic carbon (DOC), inorganic carbon (DIC) in 26 waters across the semi-humid/semi-arid Songnen Plain, China were examined with data collected during 2008-2011. Fresh (n = 14) and brackish (n = 12) waters were grouped according to electrical conductivity (threshold = 1000 μS cm-1). Significant differences in the mean DOC/DIC concentrations were observed between fresh (5.63 mg L-1, 37.39 mg L-1) and brackish waters (15.33 mg L-1, 142.93 mg L-1). Colored dissolved organic matter (CDOM) and DOC concentrations were mainly controlled by climatic-hydrologic conditions. The observation indicated that the outflow conditions in the semi-endorheic region had condensed effects on the dissolved carbon, resulting in close relationships between salinity vs. DOC (R2 = 0.66), and vs. DIC (R2 = 0.94). Independent data set collected in May 2012 also confirmed this finding (DOC: R2 = 0.79), (DIC: R2 = 0.91), highlighting the potential of quantifying DOC/DIC via salinity measurements for waters dispersed in the plain. Indices based on CDOM absorption spectra, e.g. DOC specific CDOM absorption (SUVA254), absorption ratio a250 : a365 (E250:365) and spectral slope ratio (Sr, S275-295/S350-400), were applied to characterize DOM composition and quality. Our results indicate high molecular weight CDOM fractions are more abundant in fresh waters than brackish waters.

Representation of dissolved organic carbon in the JULES land surface model (vn4.4_JULES-DOCM)

NASA Astrophysics Data System (ADS)

Nakhavali, Mahdi; Friedlingstein, Pierre; Lauerwald, Ronny; Tang, Jing; Chadburn, Sarah; Camino-Serrano, Marta; Guenet, Bertrand; Harper, Anna; Walmsley, David; Peichl, Matthias; Gielen, Bert

2018-02-01

Current global models of the carbon (C) cycle consider only vertical gas exchanges between terrestrial or oceanic reservoirs and the atmosphere, thus not considering the lateral transport of carbon from the continents to the oceans. Therefore, those models implicitly consider all of the C which is not respired to the atmosphere to be stored on land and hence overestimate the land C sink capability. A model that represents the whole continuum from atmosphere to land and into the ocean would provide a better understanding of the Earth's C cycle and hence more reliable historical or future projections. A first and critical step in that direction is to include processes representing the production and export of dissolved organic carbon in soils. Here we present an original representation of dissolved organic C (DOC) processes in the Joint UK Land Environment Simulator (JULES-DOCM) that integrates a representation of DOC production in terrestrial ecosystems based on the incomplete decomposition of organic matter, DOC decomposition within the soil column, and DOC export to the river network via leaching. The model performance is evaluated in five specific sites for which observations of soil DOC concentration are available. Results show that the model is able to reproduce the DOC concentration and controlling processes, including leaching to the riverine system, which is fundamental for integrating terrestrial and aquatic ecosystems. Future work should include the fate of exported DOC in the river system as well as DIC and POC export from soil.

The influence of slope and peatland vegetation type on riverine dissolved organic carbon and water colour at different scales.

PubMed

Parry, L E; Chapman, P J; Palmer, S M; Wallage, Z E; Wynne, H; Holden, J

2015-09-15

Peatlands are important sources of fluvial carbon. Previous research has shown that riverine dissolved organic carbon (DOC) concentrations are largely controlled by soil type. However, there has been little work to establish the controls of riverine DOC within blanket peatlands that have not undergone major disturbance from drainage or burning. A total of 119 peatland catchments were sampled for riverine DOC and water colour across three drainage basins during six repeated sampling campaigns. The topographic characteristics of each catchment were determined from digital elevation models. The dominant vegetation cover was mapped using 0.5m resolution colour infrared aerial images, with ground-truthed validation revealing 82% accuracy. Forward and backward stepwise regression modelling showed that mean slope was a strong (and negative) determinant of DOC and water colour in blanket peatland river waters. There was a weak role for plant functional type in determining DOC and water colour. At the basin scale, there were major differences between the models depending on the basin. The dominance of topographic predictors of DOC found in our study, combined with a weaker role of vegetation type, paves the way for developing improved planning tools for water companies operating in peatland catchments. Using topographic data and aerial imagery it will be possible to predict which tributaries will typically yield lower DOC concentrations and which are therefore more suitable and cost-effective as raw water intakes. Copyright © 2015 Elsevier B.V. All rights reserved.

Dissolved Organic Matter Compositional Change and Biolability During Two Storm Runoff Events in a Small Agricultural Watershed

NASA Astrophysics Data System (ADS)

Eckard, Robert S.; Pellerin, Brian A.; Bergamaschi, Brian A.; Bachand, Philip A. M.; Bachand, Sandra M.; Spencer, Robert G. M.; Hernes, Peter J.

2017-10-01

Agricultural watersheds are globally pervasive, supporting fundamentally different organic matter source, composition, and concentration profiles in comparison to natural systems. Similar to natural systems, agricultural storm runoff exports large amounts of organic carbon from agricultural land into waterways. But intense management of upper soil layers, waterway channelization, wetland and riparian habitat removal, and postharvest vegetation removal promise to uniquely drive organic matter release to waterways. During a winter first flush and a subsequent storm event, this study investigated the influence of a small agricultural watershed on dissolved organic matter (DOM) source, composition, and biolability. Storm water discharge released strongly terrestrial yet biolabile (23 to 32%) dissolved organic carbon (DOC). Following a 21 day bioassay, a parallel factor analysis identified an 80% reduction in a protein-like (phenylpropyl) component (C2) that was previously correlated to lignin phenol concentration, and a 10% reduction in a humic-like, terrestrially sourced component (C4). Storm-driven releases tripled DOC concentration (from 2.8 to 8.7 mg L-1) during the first flush event in comparison to base flow and were terrestrially sourced, with an eightfold increase in vascular plant derived lignin phenols (23.0 to 185 μg L-1). As inferred from system hydrology, lignin composition, and nitrate as a groundwater tracer, an initial pulse of dilute water from the upstream watershed caused a counterclockwise DOC hysteresis loop. DOC concentrations peaked after 3.5 days, with the delay between peak discharge and peak DOC attributed to storm water hydrology and a period of initial water repellency of agricultural soils, which delayed DOM leaching.

Evaluation of the treatment of reverse osmosis concentrates from municipal wastewater reclamation by coagulation and granular activated carbon adsorption.

PubMed

Sun, Ying-Xue; Yang, Zhe; Ye, Tao; Shi, Na; Tian, Yuan

2016-07-01

Reverse osmosis concentrate (ROC) from municipal wastewater reclamation reverse osmosis (mWRRO) contains elevated concentrations of contaminants which pose potential risks to aquatic environment. The treatment of ROC from an mWRRO using granular activated carbon (GAC) combined pretreatment of coagulation was optimized and evaluated. Among the three coagulants tested, ferric chloride (FeCl3) presented relatively higher DOC removal efficiency than polyaluminium chloride and lime at the same dosage and coagulation conditions. The removal efficiency of DOC, genotoxicity, and antiestrogenic activity concentration of the ROC could achieve 16.9, 18.9, and 39.7 %, respectively, by FeCl3 coagulation (with FeCl3 dosage of 180.22 mg/L), which can hardly reduce UV254 and genotoxicity normalized by DOC of the DOM with MW <5 kDa. However, the post-GAC adsorption column (with filtration velocity of 5.7 m/h, breakthrough point adsorption capacity of 0.22 mg DOC/g GAC) exhibited excellent removal efficiency on the dominant DOM fraction of MW <5 kDa in the ROC. The removal efficiency of DOC, UV254, and TDS in the ROC was up to 91.8, 96, and 76.5 %, respectively, by the FeCl3 coagulation and post-GAC adsorption. Also, the DOM with both genotoxicity and antiestrogenic activity were completely eliminated by the GAC adsorption. The results suggest that GAC adsorption combined pretreatment of FeCl3 coagulation as an efficient method to control organics, genotoxicity, and antiestrogenic activity in the ROC from mWRRO system.

Multi-site Field Verification of Laboratory Derived FDOM Sensor Corrections: The Good, the Bad and the Ugly

NASA Astrophysics Data System (ADS)

Saraceno, J.; Shanley, J. B.; Aulenbach, B. T.

2014-12-01

Fluorescent dissolved organic matter (FDOM) is an excellent proxy for dissolved organic carbon (DOC) in natural waters. Through this relationship, in situ FDOM can be utilized to capture both high frequency time series and long term fluxes of DOC in small streams. However, in order to calculate accurate DOC fluxes for comparison across sites, in situ FDOM data must be compensated for matrix effects. Key matrix effects, include temperature, turbidity and the inner filter effect due to color. These interferences must be compensated for to develop a reasonable relationship between FDOM and DOC. In this study, we applied laboratory-derived correction factors to real time data from the five USGS WEBB headwater streams in order to gauge their effectiveness across a range of matrix effects. The good news is that laboratory derived correction factors improved the predicative relationship (higher r2) between DOC and FDOM when compared to uncorrected data. The relative importance of each matrix effect (i.e. temperature) varied by site and by time, implying that each and every matrix effect should be compensated for when available. In general, temperature effects were more important on longer time scales, while corrections for turbidity and DOC inner filter effects were most prevalent during hydrologic events, when the highest instantaneous flux of DOC occurred. Unfortunately, even when corrected for matrix effects, in situ FDOM is a weaker predictor of DOC than A254, a common surrogate for DOC, implying that either DOC fluoresces at varying degrees (but should average out over time), that some matrix effects (e.g. pH) are either unaccounted for or laboratory-derived correction factors do not encompass the site variability of particles and organics. The least impressive finding is that the inherent dependence on three variables in the FDOM correction algorithm increases the likelihood of record data gaps which increases the uncertainty in calculated DOC flux values.

Probing dissolved organic matter in the critical zone: a comparison between in situ sampling and aqueous soil extracts

NASA Astrophysics Data System (ADS)

Perdrial, J. N.; Perdrial, N.; Harpold, A. A.; Peterson, A. M.; Vasquez, A.; Chorover, J.

2011-12-01

Analyzing dissolved organic matter (DOM) of soil solution constitutes an integral activity in critical zone science as important insights to nutrient and carbon cycling and mineral weathering processes can be gained. Soil solution can be obtained by a variety of approaches such as by in situ zero-tension and tension samplers or by performing soil extracts in the lab. It is generally preferred to obtain soil solution in situ with the least amount of disturbance. However, in water limited environments, such as in southwestern US, in situ sampling is only possible during few hydrologic events and soil extracts are often employed. In order to evaluate the performance of different sampling approaches for OM analysis, results from aqueous soil extracts were compared with in situ samples obtained from suction cups and passive capillary wick samplers (PCAP's). Soil from an OA-horizon of mixed conifer forest Jemez River Basin Critical Zone Observatory (JRB-CZO) in NM was sampled twice and in situ samples from co-located suction cups and PCAPs were collected 7 times during the 2011 snowmelt period. Dissolved organic carbon and nitrogen concentrations (DOC and DN) as well as OM quality (FTIR, fluorescence spectroscopy and PARAFAC) were analyzed. The aqueous soil extracts (solid:solution = 1:5 mass basis) showed highest DOC and lowest DN concentrations whereas samples collected in-situ had lower DOC and higher DN concentrations. PARAFAC analysis using a four component model showed a dominance of fluorescence in region I and II (protein-like fluorescence) for samples collected in situ indicating the presence of more bio-molecules (proteins). In contrast, the dominant PARAFAC component of the soil extract was found in region 3 (fulvic acid-like fluorescence). FTIR analysis showed high intensity band at 1600 cm-1 in the case of the aqueous soil extract that correspond to asymmetric stretching of carboxyl groups. These preliminary results indicate that aqueous soil extracts likely lead to the underestimation of the amount of biomolecules and the overestimation of fulvic acid contents of soil solutions.

Viscosity changes of riparian water controls diurnal fluctuations of stream-flow and DOC concentration

NASA Astrophysics Data System (ADS)

Schwab, Michael; Klaus, Julian; Pfister, Laurent; Weiler, Markus

2015-04-01

Diurnal fluctuations in stream-flow are commonly explained as being triggered by the daily evapotranspiration cycle in the riparian zone, leading to stream flow minima in the afternoon. While this trigger effect must necessarily be constrained by the extent of the growing season of vegetation, we here show evidence of daily stream flow maxima in the afternoon in a small headwater stream during the dormant season. We hypothesize that the afternoon maxima in stream flow are induced by viscosity changes of riparian water that is caused by diurnal temperature variations of the near surface groundwater in the riparian zone. The patterns were observed in the Weierbach headwater catchment in Luxembourg. The catchment is covering an area of 0.45 km2, is entirely covered by forest and is dominated by a schistous substratum. DOC concentration at the outlet of the catchment was measured with the field deployable UV-Vis spectrometer spectro::lyser (scan Messtechnik GmbH) with a high frequency of 15 minutes over several months. Discharge was measured with an ISCO 4120 Flow Logger. During the growing season, stream flow shows a frequently observed diurnal pattern with discharge minima in the afternoon. During the dormant season, a long dry period with daily air temperature amplitudes of around 10 ° C occurred in March and April 2014, with discharge maxima in the afternoon. The daily air temperature amplitude led to diurnal variations in the water temperature of the upper 10 cm of the riparian zone. Higher riparian water temperatures cause a decrease in water viscosity and according to the Hagen-Poiseuille equation, the volumetric flow rate is inversely proportional to viscosity. Based on the Hagen-Poiseuille equation and the viscosity changes of water, we calculated higher flow rates of near surface groundwater through the riparian zone into the stream in the afternoon which explains the stream flow maxima in the afternoon. With the start of the growing season, the viscosity induced diurnal effect is overlain by the stronger influence of evapotranspiration. Diurnal DOC fluctuations show daily maxima in the afternoon. While daily variations in DOC concentrations are often explained by faster in-stream biogeochemical processes during daylight, we here propose that the viscosity effect in the riparian zone could explain the afternoon peaks in DOC concentrations. Our records show that daily water temperature variations and therefore viscosity changes only occur in the near surface parts of the riparian zone, where the DOC concentrations are higher than in deeper parts of the riparian zone. We calculated, that the viscosity induced higher flow rates from the near surface parts of the riparian zone can explain the DOC concentration maxima in the afternoon. As the viscosity effect does not disappear during the growing season but is just smaller than the evapotranspiration effect, the DOC concentration pattern is not changing between the dormant and growing seasons. The different controls of diurnal fluctuations of stream-flow and water quality concentrations need to be carefully considered in order to better understand the different patterns in catchment hydrology.

Transformations and Fates of Terrigenous Dissolved Organic Matter in River-influenced Ocean Margins

NASA Astrophysics Data System (ADS)

Fichot, Cedric G.

Rivers contribute about 0.25 Pg of terrigenous dissolved organic carbon (tDOC) to the ocean each year. The fate and transformations of this material have important ramifications for the metabolic state of the ocean, air-sea CO2 exchange, and the global carbon cycle. Stable isotopic compositions and terrestrial biomarkers suggest tDOC must be efficiently mineralized in ocean margins. Nonetheless, the extent of tDOC mineralization in these environments remains unknown, as no quantitative estimate is available. The complex interplay of biogeochemical and physical processes in these systems compounded by the limited practicality of chemical proxies (organic biomarkers, isotopic compositions) make the quantification of tDOC mineralization in these dynamic systems particularly challenging. In this dissertation, new optical proxies were developed (Chapters 1 and 2) and facilitated the first quantitative assessment of tDOC mineralization in a dynamic river-influenced ocean margin (Chapter 3) and the monitoring of continental runoff distributions in the coastal ocean using remote sensing (Chapter 4). The optical properties of chromophoric dissolved organic matter (CDOM) were used as optical proxies for dissolved organic carbon concentration ([DOC]) and %tDOC. In both proxies, the CDOM spectral slope coefficient ( S275-295) was exploited for its informative properties on the chemical nature and composition of dissolved organic matter. In the first proxy, a strong relationship between S275-295 and the ratio of CDOM absorption to [DOC] facilitated accurate retrieval (+/- 4%) of [DOC] from CDOM. In the second proxy, the existence of a strong relationship between S275-295 and the DOC-normalized lignin yield facilitated the estimation of the %tDOC from S 275-295. Using the proxies, the tDOC concentration can be retrieved solely from CDOM absorption coefficients (lambda = 275-295 nm) in river-influenced ocean margins. The practicality of optical proxies facilitated the calculation of tDOC mineralization rates on the Louisiana shelf. Seasonal tDOC mass balances for the shelf revealed that between 26% (winter) and 71% (summer) of the mixed layer tDOC is mineralized during its residence on the shelf. Independent approaches further indicated biomineralization accounts for 60% of the tDOC mineralization whereas photomineralization contributes only 8%. The remaining 32% was attributed to the coupled photo-biomineralization. On an annual basis, our results indicated ˜40% of the tDOC discharged by the Mississippi and Atchafalaya rivers to the Louisiana shelf (˜1 Tg tDOC) is mineralized within 2 to 3 months. This extensive mineralization on the shelf is direct evidence ocean margins act as efficient filters of tDOC between the land and ocean. Finally, the amenability of S275-295 to ocean color remote sensing was demonstrated, and facilitates the real-time, synoptic monitoring of tDOC and freshwater runoff in coastal waters. Implementation of this approach provided the first pan-Arctic distributions of tDOC and continental runoff in surface polar waters, and will help understand the manifestations of climate change in this remote region.

Structural properties of dissolved organic carbon in deep soil horizons of an arable and temporarily grassland.

NASA Astrophysics Data System (ADS)

Lavaud, A.; Chabbi, A.; Croue, J. P.

2009-04-01

It is commonly accepted that dissolved organic carbon (DOC) is the bio-available fraction of the largest amount of soil organic matter (SOM), even if it does represent only a very small proportion. Because most of the studies on DOC dynamics were mainly restricted to forest soils, studies on the factors governing the dynamics of DOC in deep soil horizons (>1 m) in arable system are still very little limited. The objective of this work is to better define the proportion of DOC in deep soil horizons and indicate their main characteristics and structural properties. The study was conducted on the long term observatory for environmental research- biogeochemical cycles and biodiversity Lusignan site). DOC collected using lysimeters plates inserted to a depth of 105 cm was fractionated into 3 fractions using the two column array of XAD-8 and XAD-4 resins. The HPO (hydrophobic) fraction (i.e. humic substances) isolated from the XAD-8 resin, the TPH (Transphilic) fraction from the XAD-4 resin and the HPI (hydrophilic) fraction which corresponds to the DOC that does not adsorbed onto the two resins under the acid condition used (pH 2). DOM adsorbed onto the resins is recovered with a 75%/25% acetonitrile/water mixture and lyophilized. Depend on the amount of material; the chemical composition of DOC was performed using UV254 nm, fluorescence EEM, NMR and HPSEC/UV/COD. The results show that the concentration and structural properties of DOC in deep soil horizon were similar to those of groundwater (low SUVA (1.2 m-1.L.mg C-1), structures composed mainly of low molecular weight). Because of the relatively recent establishment of the treatment, the monitoring of the dynamics of the DOC concentrations did not show significant differences between arable and grassland. However, the temporal dynamic shows a slight increase in the DOC content regardless of the of land use. DOC concentrations between winter and the middle of spring tend to double going from 1 to 2.5 mg / L and then to 4-5 mg / L in summer time. The structural analysis reveals significant input of terpenoid derived organic matter was confirmed in the HPO fraction of DOC a results supported by the data of 13C NMR, Infra Red and Micro Scale Sealed Vessel / pyrolysis GC / MS. The chromatographic profiles obtained by flash pyrolysis GC / MS highlight the presence of phenol and alkyl phenols, generally attributed to structures polyhydroxyaromatiques (lignin / tannins), but acetamide, pyrolysis product of amino sugars constituents of the wall microbial cells. The thermochimiolyse (TMAH) / GC / MS confirmed the presence of hydroxy aromatic structures in the extracts, however, their precise origin (lignin, tannins ...) remains uncertain. The results so far indicate that the DOC in deep soil horizons is marked by low aromaticity and dominated by small size molecules. This would consist of carbon derived from terpenoids, lignin degraded and amino sugars.

Deep nitrogen acquisition in warming permafrost soils: Contributions of belowground plant traits and fungal symbioses in the permafrost carbon feedback to climate

NASA Astrophysics Data System (ADS)

Hartnett, H. E.; Palta, M. M.; Grimm, N. B.; Ruhi, A.; van Shaijik, M.

2016-12-01

Tempe Town Lake (TTL) is a hydrologically-regulated reservoir in Tempe, Arizona. The lake has high primary production and receives dissolved organic carbon (DOC) from rainfall, storm flow, and upstream river discharge. We applied an ARIMA time-series model to a three-year period for which we have high-frequency chemistry, meteorology, and streamflow data and analyzed external (rainfall, stream flow) and internal (dissolved O2) drivers of DOC content and composition. DOC composition was represented by fluorescence-based indices (fluorescence index, humification index, freshness) related to DOC source (microbially- vs. terrestrially-derived) and reactivity DOC. Patterns in DOC concentration and composition suggest carbon cycling in the lake responds to both meteorological events and to anthropogenic activity. The fluorescence-derived DOC composition is consistent with seasonally-distinct inputs of algal- and terrestrially-derived carbon. For example, Tempe Town Lake is supersaturated in O2 over 70% of the time, suggesting the system is autotrophic and primary productivity (i.e., O2 saturation state) was the strongest driver of DOC concentration. In contrast, external drivers (rainfall pattern, streamflow) were the strongest determinants of DOC composition. Biological processes (e.g., algal growth) generate carbon in the lake during spring and summer, and high Fluorescence Index and Freshness values at this time are indicative of algal-derived material; these parameters generally decrease with rain or flow suggesting algal-derived carbon is diluted by external water inputs. During dry periods, carbon builds up on the land surface and subsequent rainfall events deliver terrestrial carbon to the lake. Further evidence that rain and streamflow deliver land-derived material are increases in the Humification Index (an indicator of terrestrial material) following rain/flow events. Our results indicate that Tempe Town Lake generates autochthonous carbon and has the capacity to process allochthonous carbon from the urban environment. Ongoing work is comparing these results to other periods in the 10-year time series to test if the driver-DOC relationships are robust over longer time-scales and evaluating how changes in lake management and climate have altered DOC over time.

Temporal Patterns in Dissolved Organic Carbon Composition in an Urban Lake

NASA Astrophysics Data System (ADS)

Hartnett, H. E.; Palta, M. M.; Grimm, N. B.; Ruhi, A.; van Shaijik, M.

2017-12-01

Tempe Town Lake (TTL) is a hydrologically-regulated reservoir in Tempe, Arizona. The lake has high primary production and receives dissolved organic carbon (DOC) from rainfall, storm flow, and upstream river discharge. We applied an ARIMA time-series model to a three-year period for which we have high-frequency chemistry, meteorology, and streamflow data and analyzed external (rainfall, stream flow) and internal (dissolved O2) drivers of DOC content and composition. DOC composition was represented by fluorescence-based indices (fluorescence index, humification index, freshness) related to DOC source (microbially- vs. terrestrially-derived) and reactivity DOC. Patterns in DOC concentration and composition suggest carbon cycling in the lake responds to both meteorological events and to anthropogenic activity. The fluorescence-derived DOC composition is consistent with seasonally-distinct inputs of algal- and terrestrially-derived carbon. For example, Tempe Town Lake is supersaturated in O2 over 70% of the time, suggesting the system is autotrophic and primary productivity (i.e., O2 saturation state) was the strongest driver of DOC concentration. In contrast, external drivers (rainfall pattern, streamflow) were the strongest determinants of DOC composition. Biological processes (e.g., algal growth) generate carbon in the lake during spring and summer, and high Fluorescence Index and Freshness values at this time are indicative of algal-derived material; these parameters generally decrease with rain or flow suggesting algal-derived carbon is diluted by external water inputs. During dry periods, carbon builds up on the land surface and subsequent rainfall events deliver terrestrial carbon to the lake. Further evidence that rain and streamflow deliver land-derived material are increases in the Humification Index (an indicator of terrestrial material) following rain/flow events. Our results indicate that Tempe Town Lake generates autochthonous carbon and has the capacity to process allochthonous carbon from the urban environment. Ongoing work is comparing these results to other periods in the 10-year time series to test if the driver-DOC relationships are robust over longer time-scales and evaluating how changes in lake management and climate have altered DOC over time.

Simulating dissolved organic carbon dynamics at the swedish integrated monitoring sites with the integrated catchments model for carbon, INCA-C.

PubMed

Futter, M N; Löfgren, S; Köhler, S J; Lundin, L; Moldan, F; Bringmark, L

2011-12-01

Surface water concentrations of dissolved organic carbon ([DOC]) are changing throughout the northern hemisphere due to changes in climate, land use and acid deposition. However, the relative importance of these drivers is unclear. Here, we use the Integrated Catchments model for Carbon (INCA-C) to simulate long-term (1996-2008) streamwater [DOC] at the four Swedish integrated monitoring (IM) sites. These are unmanaged headwater catchments with old-growth forests and no major changes in land use. Daily, seasonal and long-term variations in streamwater [DOC] driven by runoff, seasonal temperature and atmospheric sulfate (SO₄(2-)) deposition were observed at all sites. Using INCA-C, it was possible to reproduce observed patterns of variability in streamwater [DOC] at the four IM sites. Runoff was found to be the main short-term control on [DOC]. Seasonal patterns in [DOC] were controlled primarily by soil temperature. Measured SO₄(2-) deposition explained some of the long-term [DOC] variability at all sites.

Dissolved organic carbon and major and trace elements in peat porewater of sporadic, discontinuous, and continuous permafrost zones of western Siberia

NASA Astrophysics Data System (ADS)

Raudina, Tatiana V.; Loiko, Sergey V.; Lim, Artyom G.; Krickov, Ivan V.; Shirokova, Liudmila S.; Istigechev, Georgy I.; Kuzmina, Daria M.; Kulizhsky, Sergey P.; Vorobyev, Sergey N.; Pokrovsky, Oleg S.

2017-07-01

Mobilization of dissolved organic carbon (DOC) and related trace elements (TEs) from the frozen peat to surface waters in the permafrost zone is expected to enhance under ongoing permafrost thaw and active layer thickness (ALT) deepening in high-latitude regions. The interstitial soil solutions are efficient tracers of ongoing bio-geochemical processes in the critical zone and can help to decipher the intensity of carbon and metals migration from the soil to the rivers and further to the ocean. To this end, we collected, across a 640 km latitudinal transect of the sporadic to continuous permafrost zone of western Siberia peatlands, soil porewaters from 30 cm depth using suction cups and we analyzed DOC, dissolved inorganic carbon (DIC), and 40 major elements and TEs in 0.45 µm filtered fraction of 80 soil porewaters. Despite an expected decrease in the intensity of DOC and TE mobilization from the soil and vegetation litter to the interstitial fluids with the increase in the permafrost coverage and a decrease in the annual temperature and ALT, the DOC and many major and trace elements did not exhibit any distinct decrease in concentration along the latitudinal transect from 62.2 to 67.4° N. The DOC demonstrated a maximum of concentration at 66° N, on the border of the discontinuous/continuous permafrost zone, whereas the DOC concentration in peat soil solutions from the continuous permafrost zone was equal to or higher than that in the sporadic/discontinuous permafrost zone. Moreover, a number of major (Ca, Mg) and trace (Al, Ti, Sr, Ga, rare earth elements (REEs), Zr, Hf, Th) elements exhibited an increasing, not decreasing, northward concentration trend. We hypothesize that the effects of temperature and thickness of the ALT are of secondary importance relative to the leaching capacity of peat, which is in turn controlled by the water saturation of the peat core. The water residence time in peat pores also plays a role in enriching the fluids in some elements: the DOC, V, Cu, Pb, REEs, and Th were a factor of 1.5 to 2.0 higher in mounds relative to hollows. As such, it is possible that the time of reaction between the peat and downward infiltrating waters essentially controls the degree of peat porewater enrichments in DOC and other solutes. A 2° northward shift in the position of the permafrost boundaries may bring about a factor of 1.3 ± 0.2 decrease in Ca, Mg, Sr, Al, Fe, Ti, Mn, Ni, Co, V, Zr, Hf, Th, and REE porewater concentration in continuous and discontinuous permafrost zones, and a possible decrease in DOC, specific ultraviolet absorbency (SUVA), Ca, Mg, Fe, and Sr will not exceed 20 % of their current values. The projected increase in ALT and vegetation density, northward migration of the permafrost boundary, or the change of hydrological regime is unlikely to modify chemical composition of peat porewater fluids larger than their natural variations within different micro-landscapes, i.e., within a factor of 2. The decrease in DOC and metal delivery to small rivers and lakes by peat soil leachate may also decrease the overall export of dissolved components from the continuous permafrost zone to the Arctic Ocean. This challenges the current paradigm on the increase in DOC export from the land to the ocean under climate warming in high latitudes.

The impact of four decades of annual nitrogen addition on dissolved organic matter in a boreal forest soil

NASA Astrophysics Data System (ADS)

Rappe-George, M. O.; Gärdenäs, A. I.; Kleja, D. B.

2012-09-01

Addition of mineral nitrogen (N) can alter the concentration and quality of dissolved organic matter (DOM) in forest soils. The aim of this study was to assess the effect of long-term mineral N addition on soil solution concentration of dissolved organic carbon (DOC) and dissolved organic nitrogen (DON) in the Stråsan experimental forest (Norway spruce) in Central Sweden. N was added yearly at two levels of intensity and duration: the N1 treatment represented a lower intensity, but a longer duration (43 yr) of N addition than the shorter N2 treatment (24 yr). N additions were terminated in the N2 treatment in 1991. The N treatments began in 1967 when the spruce stands were 9 yr old. Soil solution in the forest floor O, and soil mineral B, horizons were sampled during the growing seasons of 1995 and 2009. Tension and non-tension lysimeters were installed in the O horizon (n=6) and tension lysimeters were installed in the underlying B horizon (n=4): soil solution was sampled at two-week intervals. Although tree growth and O horizon carbon (C) and N stock increased in treatments N1 and N2, the concentration of DOC in O horizon leachates was similar in both N treatments and control. This suggests an inhibitory direct effect of N addition on O horizon DOC. Elevated DON and nitrate in O horizon leachates in the ongoing N1 treatment indicated a move towards N saturation. In B-horizon leachates, the N1 treatment approximately doubled leachate concentration of DOC and DON. DON returned to control levels but DOC remained elevated in B-horizon leachates in N2 plots 19 yr after termination of N addition. Increased aromaticity of the sampled DOM in mineral B horizon in both the ongoing and terminated N treatment indicated that old SOM in the mineral soil was a source of the increased DOC.

Characterizing Groundwater Sources of Organic Matter to Arctic Coastal Waters

NASA Astrophysics Data System (ADS)

Connolly, C. T.; Spencer, R. G.; Cardenas, M. B.; Bennett, P. C.; McNichol, A. P.; McClelland, J. W.

2016-12-01

The Arctic is projected to transition from a runoff-dominated system to a groundwater-dominated system as permafrost thaws due to climate change. This fundamental shift in hydrology is expected to increase groundwater flow to Arctic coastal waters, which may be a significant source of dissolved organic matter (DOM) to these waters—even under present conditions—that has been largely overlooked. Here we quantify and elucidate sources of groundwater DOM inputs to lagoons along the eastern Alaskan Beaufort Sea coast using an approach that combines concentration measurements and radiocarbon dating of groundwater, soil profiles, and soil leachable dissolved organic carbon (DOC). Samples were collected in late summer, when soil thaw depths (active layer) were near their maximum extent. As anticipated, the radiocarbon age of bulk soil organic matter increased with depth (modern - 6,100 yBP), while the amount of extractable DOC decreased with depth within the active layer. However, amounts of extractable DOC increased dramatically in thawed permafrost samples collected directly below the actively layer. Concentrations of DOM in groundwater (ranging from 902 to 5,118 μmolL-1 DOC) are one to two orders of magnitude higher than those measured in lagoons and nearby river water. In contrast, the 14C-DOC ages of groundwater (1,400 ± 718 s.d. yBP), lagoon water (1,750 yBP), and river water (1,610 yBP) are comparable. Together these results suggest that: (1) groundwater provides a highly concentrated input of old DOC to Arctic coastal waters; (2) groundwater DOM is likely sourced from organic matter spanning the entire soil profile; and (3) the DOM in rivers along the eastern Alaskan Beaufort Sea coast during late summer is strongly influenced by groundwater sources, but is much lower in concentration due to photo-mineralization and/or biological consumption. These results are key for assessing how changes in land-ocean export of organic matter as permafrost thaws will change into the future with clear ramifications for Arctic coastal environments.

Dissolved Organic Carbon and Natural Terrestrial Sequestration Potential in Volcanic Terrain, San Juan Mountains, Colorado

NASA Astrophysics Data System (ADS)

Yager, D. B.; Burchell, A.; Johnson, R. H.; Kugel, M.; Aiken, G.; Dick, R.

2009-12-01

The need to reduce atmospheric CO2 levels has stimulated studies to understand and quantify carbon sinks and sources. Soils represent a potentially significant natural terrestrial carbon sequestration (NTS) reservoir. This project is part of a collaborative effort to characterize carbon (C) stability in temperate soils. To examine the potential for dissolved organic carbon (DOC) values as a qualitative indicator of C-stability, peak-flow (1500 ft3/s) and low-flow (200 ft3/s) samples from surface and ground waters were measured for DOC. DOC concentrations are generally low. Median peak-flow values from all sample sites (mg/L) were: streams (0.9); seeps (1.2); wells (0.45). Median low-flow values were: streams (0.7); seeps (0.75); wells (0.5). Median DOC values decrease between June and September 0.45 mg/L for seeps, and 0.2 mg/L for streams. Elevated DOC in some ground waters as compared to surface waters indicates increased contact time with soil organic matter. Elevated peak-flow DOC in areas with propylitically-altered bedrocks, composed of a secondary acid neutralizing assemblage of calcite-chlorite-epidote, reflects increased microbial and vegetation activity as compared to reduced organic matter accumulation in highly-altered terrain composed of an acid generating assemblage with abundant pyrite. Waters sampled in propylitically-altered bedrock terrain exhibit the lowest values during low-flow and suggest bedrock alteration type may influence DOC. Previous studies revealed undisturbed soils sampled have 2 to 6 times greater total organic soil carbon (TOSC) than global averages. Forest soils underlain by intermediate to mafic volcanic bedrock have the highest C (34.15 wt%), C: N (43) and arylsulfatase enzyme activity (ave. 278, high 461 µg p-nitrophenol/g/h). Unreclaimed mine sites have the lowest C (0 to 0.78 wt%), and arylsulfatase enzyme activity (0 to 41). Radiocarbon dates on charcoal collected from paleo-burn horizons illustrate Rocky Mountain soils may represent an old and if undisturbed, stable carbon pool (500 -5,440 ± 40 yrs B.P). Undisturbed and reclaimed soils derived from propylitic bedrocks also exhibit high TOSC (13.5 - 25.6 wt%), C: N (27), arylsulfatase (338). This is consistent with earlier studies in which propylitic bedrocks were identified as having a high acid-neutralizing capacity (ANC). Observations at natural reclamation sites suggest “bio-geo-mimicry” techniques that use ANC rock plus other soil amendments (biochar, nutrients, mycorrhizea, seeding) may aid reclamation measures and support carbon sequestration. The data demonstrate that volcanic-hosted watersheds may exhibit both high TOSC and low DOC. This is attributed to: host rock-weathering release of nutrients important for soil productivity, ANC, formation of secondary mineral carbonates; development of intermediate soil aggregates and adsorption-enhancing clays that stabilize C and N, environmental factors such as climate, moisture retention, and land use. Future work will explore the potential of DOC flux as a proxy for NTS potential.

How Redox Fluctuation Shapes Microbial Community Structure and Mineral-Organic Matter Relationships in a Humid Tropical Forest Soil

NASA Astrophysics Data System (ADS)

Campbell, A.; Bhattacharyya, A.; Lin, Y.; Tfaily, M. M.; Paša-Tolić, L.; Chu, R. K.; Silver, W. L.; Nico, P. S.; Pett-Ridge, J.

2016-12-01

Wet tropical soils can alternate frequently between fully oxygenated and anaerobic conditions, constraining both the metabolism of tropical soil microorganisms, and the mineral-organic matter relationships that regulate many aspects of soil C cycling. Tropical forests are predicted to experience a 2-5°C temperature increase and substantial differences in the amount and timing of rainfall in the coming half century. Yet we have a poor understanding of how soil microbial activity and C cycling in these systems will respond to changes in environmental variability caused by climate change. Using a 44 day redox manipulation and isotope tracing experiment with soils from the Luquillo Experimental Forest, Puerto Rico, we examined patterns of tropical soil microorganisms, metabolites and soil chemistry when soils were exposed to different redox regimes - static oxic, static anoxic, high frequency redox fluctuation (4 days oxic, 4 days anoxic), or low frequency redox fluctuation (8 days oxic, 4 days anoxic). Replicate microcosms were harvested throughout the incubation to understand how changes in redox oscillation frequency altered microbial community structure and activity, organic matter turnover and fate, and soil chemistry. While gross soil respiration was highest in static oxic soils, respiration derived from added litter was highest in static anoxic soils, suggesting that decomposition of preexisting SOM was limited by O2 availability in the anoxic treatment. Microbial communities responded to shifting O2 availability in the different treatments, resulting in significant differences in DOC concentration and molecular composition (measured by FTICR-MS). DOC and Fe2+ concentrations were positively correlated for all four redox treatments, and rapidly increased following oscillation from oxic to anoxic conditions. These results, along with parallel studies of biogeochemical responses (Fe speciation, pH, P availability), suggest a highly responsive microbial and geochemical system, where the frequency of low-redox events controls exchanges of C between mineral-sorbed and aqueous pools.

Conceptualizing the seasonal and hydrological dynamics of riparian zone control on DOC in boreal headwater streams

NASA Astrophysics Data System (ADS)

Winterdahl, M.; Laudon, H.; Köhler, S.; Seibert, J.; Bishop, K.

2009-04-01

Dissolved organic material (DOM) plays a key role in many natural surface waters. Despite the importance of DOC for the hydrochemistry in boreal headwaters there are few models that conceptualize the controls on short-term variability in stream DOC. A relatively simple model has been proposed where the vertical profile of DOC in the riparian soil solution, serves as an instantaneous "chemostat" setting the DOC of laterally flowing groundwater just before it enters the stream. This paper considers whether the addition of seasonality (in the form of soil temperature) and antecedent flows can improve the predictions of daily DOC concentrations. The model was developed and tested using field data from the Krycklan catchment on the Svartberget Research Station in northern Sweden where a transect of soil solution sampling sites equipped with suction lysimeters and wells for monitoring groundwater level have been installed and monitored for over a decade. The field data showed an exponential correlation between depth and DOC concentration in the soil solution. There was also an exponential correlation between stream discharge and groundwater table position. The expressions for these two correlations (exponential functions) have been combined into a simple riparian DOC model. To simulate effects of seasonality and/or antecedent flow, modules for soil temperature evolution and/or groundwater flow were added and tested. The model was calibrated and tested against 8 years of data from the Västrabäcken headwater catchment in the Krycklan area. To estimate the uncertainty in the model and the observed data a Hornberger-Spear-Young sensitivity analysis together with a GLUE uncertainty analysis was performed.

Shifts in vegetation affect organic carbon quality in a coastal marsh along the Hudson River Estuary

NASA Astrophysics Data System (ADS)

Zhang, A. H.; Corbett, J. E.; Tfaily, M. M.; Martin, I.; Ho, L.; Sun, E.; Sevilla, L.; Vincent, S.; Newton, R.; Peteet, D. M.

2015-12-01

To better understand carbon storage in coastal salt marshes, samples were collected from Piermont Marsh, NY (40 ̊00' N, 73 ̊55'W) located within the Hudson River Estuary. Porewater from three different vegetation sites was analyzed to compare the quality of the dissolved organic carbon. Sites contained either native or invasive vegetation with variations in live plant root depth. Porewater was taken from 0-3m in 50cm intervals, and sites were dominated either by invasive Phragmites australis, native Eleocharis , or native mixed vegetation (Spartina patens, Scirpus, and Typha angustifolia). Sites dominated by invasive Phragmites australis were found to have lower dissolved organic carbon (DOC) concentrations, lower cDOM absorption values, and more labile organic carbon compounds. The molecular composition of the DOC was determined with Fourier Transform Ion Cyclotron Mass Spectrometry (FT-ICR-MS). Labile DOC components were defined as proteins, carbohydrates, and amino sugars while recalcitrant DOC components were defined as lipids, unsaturated hydrocarbons, lignins, tannins, and condensed hydrocarbons. For the Phragmites, Eleocharis, and mixed vegetation sites, average DOC concentrations with depth were found to be 1.71 ± 1.06, 4.64 ± 1.73, and 4.62 ± 3.5 (mM), respectively and cDOM absorption values with depth were found to be 13.22 ± 4.81, 49.42 ± 10.8, and 35.74 ± 17.49 (m-1). Additionally, DOC concentrations increased with depth in the mixed vegetation and Eleocharis sites, but remained relatively constant in the Phragmites site. The percent of labile compounds in the surface samples were found to be 19.02, 14.64, and 14.07% for the Phragmites, Eleocharis, and mixed vegetation sites, respectively. These findings suggest that sites dominated by Phragmites may have more reactive DOC substrates than sites dominated by native vegetation. These results indicate that the carbon storage in marshes invaded by Phragmites would be expected to decrease over time.

Stream Water, Carbon and Total Nitrogen Load Responses to a Simulated Emerald Ash Borer Infestation in Black Ash Dominated Headwater Wetlands

NASA Astrophysics Data System (ADS)

Van Grinsven, M. J.; Shannon, J.; Noh, N. J.; Kane, E. S.; Bolton, N. W.; Davis, J.; Wagenbrenner, J.; Sebestyen, S. D.; Kolka, R.; Pypker, T. G.

2017-12-01

The rapid and extensive expansion of emerald ash borer (EAB) is considered an important ecological and economic disturbance, and will likely affect critical ecosystem services associated with black ash wetlands. It is unknown how EAB-induced disturbance in wetlands dominated with black ash will impact stream water, dissolved organic carbon (DOC) and total dissolved nitrogen (TDN) export dynamics. We hypothesized that loads of water, DOC and TDN exported from black ash wetlands would be elevated following an EAB-induced disturbance. Stream water, DOC and TDN loads exiting two black ash wetlands in headwater watersheds in Michigan were quantified over a four-year period, and were combined with wetland soil temperature and soil decomposition rate monitoring to better understand the biogeochemical implications of an EAB-induced disturbance. After a two-year baseline monitoring period, an EAB disturbance was simulated by felling (ash-cut) all black ash trees with diameters greater than 2.5-cm in one wetland. When compared to the unaltered control, stream water DOC and TDN concentrations exiting the ash-cut wetland were significantly larger by 39% and 38%, respectively during the post-treatment study period. The significantly elevated DOC and TDN concentrations were likely associated with the higher soil temperatures and increased rates of soil decomposition detected in the ash-cut site during the post-treatment period. No significant mean daily stream discharge differences were detected between treatments during the pre-treatment period, however the 0.46 mm d-1 mean daily stream discharge exiting the ash-cut wetland was significantly smaller than the 1.07 mm d-1 exiting the unaltered control during the post-treatment study period. The significantly smaller daily stream discharge in the ash-cut site likely contributed to the fact no significant differences between treatments for either mean daily DOC loads or TDN loads were detected during the post-treatment period, despite the detection of significantly higher DOC and TDN concentrations. Examination of seasonal stream water, DOC and TDN export dynamics revealed the relative magnitudes of EAB-induced impacts were not evenly distributed throughout the year, and these differences have distinct seasonal implications for downstream waterbodies.

Nitrate loading and CH4 and N2O Flux from headwater streams

NASA Astrophysics Data System (ADS)

Sousa, C. H. R. D.; Hilker, T.; Hall, F. G.; Moura, Y. M.; McAdam, E.

2014-12-01

Freshwater ecosystems transport and process significant amounts of terrestrial carbon and can be considerable sources of CO2, CH4, and N2O. A great deal of uncertainty, however, remains in both global estimates and our understanding of drivers of freshwater greenhouse gas emissions. Furthermore, small headwater streams have received insufficient attention to date and may contribute disproportionately to global GHG flux. Our objective was to quantify GHG flux and assess the impact of changes in DOC and NO3 concentrations in surface and subsurface water on flux rates in three streams in the Lamprey River watershed in New Hampshire, USA, that contrast in surface water DOC:NO3. We measured DOC, NO3 and dissolved gas concentrations in surface waters of each stream monthly from May 2011 to April 2012. Empirical measurements of reaeration coefficients were used to convert dissolved gas concentrations to fluxes. We found higher GHG concentrations and fluxes in the two streams with high DOC concentrations, particularly gases produced by anaerobic metabolism (CH4, N2O from methanogenesis and denitrification, respectively). The stream with high DOC and high NO3 showed high N2O and low CH4 flux, while the high DOC, low NO3 stream showed high CH4 and low N2O flux. Our results are consistent with a model in which C inputs drive total GHG production, while NO3 input regulates the relative importance of CH4 and N2O by suppressing methanogenesis and stimulating denitrification. The magnitude of GHG fluxes suggests that streams in this region are likely to be small sources of CO2, but potentially important sources of CH4 and N2O. Since CH4 and N2O are many times more powerful than CO2 at trapping heat in the atmosphere, freshwater emissions of these gases have the potential to offset a significant proportion of the climate benefits of the terrestrial carbon sink, a possibility that has not been sufficiently incorporated into climate models.

Nitrate loading and CH4 and N2O Flux from headwater streams

NASA Astrophysics Data System (ADS)

Schade, J. D.; Bailio, J.; McDowell, W. H.

2015-12-01

Freshwater ecosystems transport and process significant amounts of terrestrial carbon and can be considerable sources of CO2, CH4, and N2O. A great deal of uncertainty, however, remains in both global estimates and our understanding of drivers of freshwater greenhouse gas emissions. Furthermore, small headwater streams have received insufficient attention to date and may contribute disproportionately to global GHG flux. Our objective was to quantify GHG flux and assess the impact of changes in DOC and NO3 concentrations in surface and subsurface water on flux rates in three streams in the Lamprey River watershed in New Hampshire, USA, that contrast in surface water DOC:NO3. We measured DOC, NO3 and dissolved gas concentrations in surface waters of each stream monthly from May 2011 to April 2012. Empirical measurements of reaeration coefficients were used to convert dissolved gas concentrations to fluxes. We found higher GHG concentrations and fluxes in the two streams with high DOC concentrations, particularly gases produced by anaerobic metabolism (CH4, N2O from methanogenesis and denitrification, respectively). The stream with high DOC and high NO3 showed high N2O and low CH4 flux, while the high DOC, low NO3 stream showed high CH4 and low N2O flux. Our results are consistent with a model in which C inputs drive total GHG production, while NO3 input regulates the relative importance of CH4 and N2O by suppressing methanogenesis and stimulating denitrification. The magnitude of GHG fluxes suggests that streams in this region are likely to be small sources of CO2, but potentially important sources of CH4 and N2O. Since CH4 and N2O are many times more powerful than CO2 at trapping heat in the atmosphere, freshwater emissions of these gases have the potential to offset a significant proportion of the climate benefits of the terrestrial carbon sink, a possibility that has not been sufficiently incorporated into climate models.

Understanding the relationship between DOC and nitrate export and dominant rainfall-runoff processes through long-term high frequency measurements

NASA Astrophysics Data System (ADS)

Schwab, Michael; Klaus, Julian; Pfister, Laurent; Weiler, Markus

2016-04-01

Over the past decades, stream sampling protocols for hydro-geochemical parameters were often limited by logistical and technological constraints. While long-term monitoring protocols were typically based on weekly sampling intervals, high frequency sampling was commonly limited to a few single events. In our study, we combined high frequency and long-term measurements to understand the DOC and nitrate behaviour and dynamics for different runoff events and seasons. Our study area is the forested Weierbach catchment (0.47 km2) in Luxembourg. The fractured schist bedrock is covered by cambisol soils. The runoff response of the catchment is characterized by a double peak behaviour. A first discharge peak occurs during or right after a rainfall event (triggered by fast near surface runoff generation processes), while a second delayed peak lasts several days (generated by subsurface flow/ shallow groundwater flow). Peaks in DOC concentrations are closely linked to the first discharge peak, whereas nitrate concentrations follow the second peak. Our observations were carried out with the field deployable instrument spectro::lyser (scan Messtechnik GmbH). This instrument relies on the principles of UV-Vis spectrometry and measures DOC and nitrate concentrations. The measurements were carried out at a high frequency of 15 minutes in situ in the Weierbach creek for more than two years. In addition, a long-term validation was carried out with data obtained from the analysis of water collected with automatic samplers. The long-term, high-frequency measurements allowed us to calculate a complete and detailed balance of DOC and nitrate export over two years. Transport behaviour of the DOC and nitrate showed different dynamics between the first and second hydrograph peaks. DOC is mainly exported during first peaks, while nitrate is mostly exported during the delayed second peaks. In combination with other measurements in the catchment, the long and detailed observations have enabled us to derive relationships between DOC and nitrate export and different catchment states: soil wetness and groundwater levels, precipitation and seasonality. Altogether, the long-term and high-frequency time series provides the opportunity to study DOC and nitrate export without having to just rely only on either a few single event measurements or coarse measurement protocols.

The river as a chemostat: fresh perspectives on dissolved organic matter flowing down the river continuum

USGS Publications Warehouse

Creed, Irena F.; McKnight, Diane M.; Pellerin, Brian; Green, Mark B.; Bergamaschi, Brian; Aiken, George R.; Burns, Douglas A.; Findlay, Stuart E G; Shanley, James B.; Striegl, Robert G.; Aulenbach, Brent T.; Clow, David W.; Laudon, Hjalmar; McGlynn, Brian L.; McGuire, Kevin J.; Smith, Richard A.; Stackpoole, Sarah M.

2015-01-01

A better understanding is needed of how hydrological and biogeochemical processes control dissolved organic carbon (DOC) concentrations and dissolved organic matter (DOM) composition from headwaters downstream to large rivers. We examined a large DOM dataset from the National Water Information System of the US Geological Survey, which represents approximately 100 000 measurements of DOC concentration and DOM composition at many sites along rivers across the United States. Application of quantile regression revealed a tendency towards downstream spatial and temporal homogenization of DOC concentrations and a shift from dominance of aromatic DOM in headwaters to more aliphatic DOM downstream. The DOC concentration–discharge (C-Q) relationships at each site revealed a downstream tendency towards a slope of zero. We propose that despite complexities in river networks that have driven many revisions to the River Continuum Concept, rivers show a tendency towards chemostasis (C-Q slope of zero) because of a downstream shift from a dominance of hydrologic drivers that connect terrestrial DOM sources to streams in the headwaters towards a dominance of instream and near-stream biogeochemical processes that result in preferential losses of aromatic DOM and preferential gains of aliphatic DOM.

[Sources of dissolved organic carbon and the bioavailability of dissolved carbohydrates in the tributaries of Lake Taihu].

PubMed

Ye, Lin-Lin; Wu, Xiao-Dong; Kong, Fan-Xiang; Liu, Bo; Yan, De-Zhi

2015-03-01

Surface water samples of Yincungang and Chendonggang Rivers were collected from September 2012 to August 2013 in Lake Taihu. Water temperature, Chlorophyll a and bacterial abundance were analyzed, as well as dissolved organic carbon (DOC) concentrations, stable carbon isotope of DOC (Δ13C(DOC)), specific UV absorbance (SUVA254 ) and dissolved carbohydrates concentrations. Δ13C(DOC) ranged from -27.03% per thousand ± 0.30% per thousand to -23.38%per thousand ± 0.20% per thousand, indicating a terrestrial source. Both the autochthonous and allochthonous sources contributed to the carbohydrates pool in the tributaries. Significant differences in PCHO (polysaccharides) and MCHO (monosaccharides) concentrations were observed between spring-summer and autumn-winter (P < 0.01, n = 12; P < 0.01, n = 12), which might be caused by the variation in the sources and bioavailability of carbohydrates. PCHO contributed a major fraction to TCHO (total dissolved carbohydrates) in autumn and winter, which could be explained by the accumulation of undegradable PCHO limited by the low water temperature; MCHO contributed a major fraction to TCHO in spring and summer, which might be caused by the transformation from PCHO by microbes at high water temperature.

[Effects of simulated nitrogen deposition on organic matter leaching in forest soil].

PubMed

Duan, Lei; ma, Xiao-Xiao; Yu, De-Xiang; Tan, Bing-Quan

2013-06-01

The impact of nitrogen deposition on the dynamics of carbon pool in forest soil was studied through a field experiment at Tieshanping, Chongqing in Southwest China. The changes of dissolved organic matter (DOM) concentration in soil water in different soil layers were monitored for five years after addition of ammonium nitrate (NH4NO3) or sodium nitrate (NaNO3) at the same dose as the current nitrogen deposition to the forest floor. The results indicated that the concentration and flux of dissolved organic carbon (DOC) were increased in the first two years and then decreased by fertilizing. Fertilizing also reduced the DOC/DON (dissolved organic nitrogen) ratio of soil water in the litter layer and the DOC concentration of soil water in the upper mineral layer, but had no significant effect on DOC flux in the lower soil layer. Although there was generally no effect of increasing nitrogen deposition on the forest carbon pool during the experimental period, the shift from C-rich to N-rich DOM might occur. In addition, the species of nitrogen deposition, i. e., NH4(+) and NO3(-), did not show difference in their effect on soil DOM with the same equivalence.

Influence of dissolved organic carbon on toxicity of copper to a unionid mussel (Villosa iris) and a cladoceran (Ceriodaphnia dubia) in acute and chronic water exposures

USGS Publications Warehouse

Wang, Ning; Mebane, Christopher A.; Kunz, James L.; Ingersoll, Christopher G.; Brumbaugh, William G.; Santore, Robert C.; Gorsuch, Joseph W.; Arnold, W. Ray

2011-01-01

Acute and chronic toxicity of copper (Cu) to a unionid mussel (Villosa iris) and a cladoceran (Ceriodaphnia dubia) were determined in water exposures at four concentrations of dissolved organic carbon (DOC; nominally 0.5, 2.5, 5, and 10 mg/L as carbon [C]). Test waters with DOC concentrations of 2.5 to 10 mg C/L were prepared by mixing a concentrate of natural organic matter (Suwannee River, GA, USA) in diluted well water (hardness 100 mg/L as CaCO3, pH 8.3, DOC 0.5 mg C/L). Acute median effect concentrations (EC50s) for dissolved Cu increased approximately fivefold (15–72 μg Cu/L) for mussel survival in 4-d exposures and increased about 11-fold (25–267 μg Cu/L) for cladoceran survival in 2-d exposures across DOC concentrations from 0.5 to 10 mg C/L. Similarly, chronic 20% effect concentrations (EC20s) for the mussel in 28-d exposures increased about fivefold (13–61 μg Cu/L for survival; 8.8–38 μg Cu/L for biomass), and the EC20s for the cladoceran in 7-d exposures increased approximately 17-fold (13–215 μg Cu/L) for survival or approximately fourfold (12–42 μg Cu/L) for reproduction across DOC concentrations from 0.5 to 10 mg C/L. The acute and chronic values for the mussel were less than or approximately equal to the values for the cladoceran. Predictions from the biotic ligand model (BLM) used to derive the U.S. Environmental Protection Agency's ambient water quality criteria (AWQC) for Cu explained more than 90% of the variation in the acute and chronic endpoints for the two species, with the exception of the EC20 for cladoceran reproduction (only 46% of variation explained). The BLM-normalized acute EC50s and chronic EC20s for the mussel and BLM-normalized chronic EC20s for the cladoceran in waters with DOC concentrations of 2.5 to 10 mg C/L were equal to or less than the final acute value and final chronic value in the BLM-based AWQC for Cu, respectively, indicating that the Cu AWQC might not adequately protect the mussel from acute and chronic exposure, and the cladoceran from chronic exposure.

Chemical characteristics of dissolved organic matter (DOM) in relation to heavy metal concentrations in soil water from boreal peatlands after clear-cut harvesting

NASA Astrophysics Data System (ADS)

Kiikkilä, O.; Nieminen, T.; Starr, M.; Ukonmaanaho, L.

2012-04-01

Boreal peatlands form an important terrestrial carbon reserve and are a major source of dissolved organic matter (DOM) to surface waters, particularly when disturbed through forestry practices such as draining or timber harvesting. Heavy metals show a strong affinity to organic matter and so, along with DOM, heavy metals can be mobilized and transported from the soil to surface waters and sediments where they may become toxic to aquatic organisms and pass up the food chain. The complexation of heavy metals with DOM can be expected to be related and determined by the chemical characteristics of DOM and oxidation/reducing conditions in the peat. We extracted interstitial water from peat samples and determined the concentrations of dissolved organic carbon (DOC), dissolved organic nitrogen (DON) and Al, Cu, Zn and Fe in various fractions of DOM isolated by adsorption properties (XAD-8 fractionation) and molecular-weight (ultrafiltration). The peat samples were taken from 0-30 and 30-50 cm depth in drained peatland catchments two years after whole-tree or stem-only clear-cut harvesting (Scots pine or Norway spruce) had been carried out. The samples from the upper layer had been subject to alternating saturation/aeration conditions while the deeper layer had been continuously under the water table. The fractionation of DOC and DON according to both adsorption properties and molecular-weight fractions clearly differed between the upper and lower peat layers. While the hydrophobic acid fraction contained proportionally more DOC and DON than the hydrophilic acid fraction in the upper peat layer the results were vice versa in the lower peat layer. High-molecular-weight compounds (> 100 kDa) were proportionally more abundant in the upper and low-molecular-weight compounds (< 1 kDa) in the lower peat layer. These differences are assumed to reflect differences in the aerobic/ anaerobic conditions and degree of decomposition between the two layers. The concentrations of Zn, Al, Fe and DON correlated positively with DOC concentrations whereas the concentration Cu did not correlate with DOC concentrations. Heavy metal concentrations in different molecular-weight fractions indicated that Al, Cu, Zn and Fe were mostly associated with high-molecular-weight compounds and only a small fraction existed as free metal ions in solution. There were no clear differences in the chemical characteristics of DOC or DON or heavy metal concentrations between the two harvesting treatments.

Tracing dissolved organic carbon and trihalomethane formation potential between source water and finished drinking water at a lowland and an upland UK catchment.

PubMed

Brooks, Emma; Freeman, Christopher; Gough, Rachel; Holliman, Peter J

2015-12-15

Rising dissolved organic carbon (DOC) concentrations in many upland UK catchments represents a challenge for drinking water companies, in particular due to the role of DOC as a precursor in the formation of trihalomethanes (THMs). Whereas traditionally, the response of drinking water companies has been focussed on treatment processes, increasingly, efforts have been made to better understanding the role of land use and catchment processes in affecting drinking water quality. In this study, water quality, including DOC and THM formation potential (THMFP) was assessed between the water source and finished drinking water at an upland and a lowland catchment. Surprisingly, the lowland catchment showed much higher reservoir DOC concentrations apparently due to the influence of a fen within the catchment from where a major reservoir inflow stream originated. Seasonal variations in water quality were observed, driving changes in THMFP. However, the reservoirs in both catchments appeared to dampen these temporal fluctuations. Treatment process applied in the 2 catchments were adapted to reservoir water quality with much higher DOC and THMFP removal rates observed at the lowland water treatment works where coagulation-flocculation was applied. However, selectivity during this DOC removal stage also appeared to increase the proportion of brominated THMs produced. Copyright © 2015. Published by Elsevier B.V.

Metabolic and physiochemical responses to a whole-lake experimental increase in dissolved organic carbon in a north-temperate lake

USGS Publications Warehouse

Zwart, Jacob A.; Craig, Nicola; Kelly, Patrick T.; Sebestyen, Stephen D.; Solomon, Christopher T.; Weidel, Brian C.; Jones, Stuart E.

2016-01-01

Over the last several decades, many lakes globally have increased in dissolved organic carbon (DOC), calling into question how lake functions may respond to increasing DOC. Unfortunately, our basis for making predictions is limited to spatial surveys, modeling, and laboratory experiments, which may not accurately capture important whole-ecosystem processes. In this article, we present data on metabolic and physiochemical responses of a multiyear experimental whole-lake increase in DOC concentration. Unexpectedly, we observed an increase in pelagic gross primary production, likely due to a small increase in phosphorus as well as a surprising lack of change in epilimnetic light climate. We also speculate on the importance of lake size modifying the relationship between light climate and elevated DOC. A larger increase in ecosystem respiration resulted in an increased heterotrophy for the treatment basin. The magnitude of the increase in heterotrophy was extremely close to the excess DOC load to the treatment basin, indicating that changes in heterotrophy may be predictable if allochthonous carbon loads are well-constrained. Elevated DOC concentration also reduced thermocline and mixed layer depth and reduced whole-lake temperature. Results from this experiment were quantitatively different, and sometimes even in the opposite direction, from expectations based on cross-system surveys and bottle experiments, emphasizing the importance of whole-ecosystem experiments in understanding ecosystem response to environmental change.

A multi-residue method for the analysis of pesticides and pesticide degradates in water using HLB solid-phase extraction and gas chromatography-ion trap mass spectrometry

USGS Publications Warehouse

Hladik, M.L.; Smalling, K.L.; Kuivila, K.M.

2008-01-01

A method was developed for the analysis of over 60 pesticides and degradates in water by HLB solid-phase extraction and gas-chromatography/mass spectrometry. Method recoveries and detection limits were determined using two surface waters with different dissolved organic carbon (DOC) concentrations. In the lower DOC water, recoveries and detection limits were 80%-108% and 1-12 ng/L, respectively. In the higher DOC water, the detection limits were slightly higher (1-15 ng/L). Additionally, surface water samples from four sites were analyzed and 14 pesticides were detected with concentrations ranging from 4 to 1,200 ng/L. ?? 2008 Springer Science+Business Media, LLC.

[Key pathway of methane production and characteristics of stable carbon isotope of the Tuojia River waterbody.

PubMed

Zhao, Qiang; Lyu, Cheng Wen; Qin, Xiao Bo; Wu, Hong Bao; Wan, Yun Fan; Liao, Yu Lin; Lu, Yan Hong; Wang, Bin; Li, Yong

2018-05-01

This study aimed at exploring the key pathway of methane production and clarifying the composition and distribution of carbon (C) isotopes in the Tuojia River waterbody in Hunan Pro-vince. We estimated CH 4 concentrations and fluxes of four reaches (S 1 , S 2 , S 3 and S 4 ) by a two-layer diffusion model and gas chromatography. The spatial and temporal distribution of CH 4 flux and its relationship with environmental factors were examined. The key pathway of CH 4 production was investigated by stable C isotope method to analyze the distribution characteristics of 13 C isotope (δ 13 C) of water dissolved CH 4 and seston/benthic organic matter. There was significant seasonal variability in water pH, with mean value of (7.27±0.03). The concentration of dissolved oxygen (DO) showed strong seasonal and spatial variations, with the range of 0.43-13.99 mg·L -1 . The maximum value of DO occurred in S 1 and differed significantly in summer and autumin. In addition, DO differed significantly in winter and other seasons in S 2 , S 3 and S 4 . The concentration of dissolved organic carbon (DOC) showed a gradual increasing trend from source to estuary. The highest concentration of DOC (8.32 mg·L -1 ) was found in S 2 , while the lowest was observed in S 1 (0.34 mg·L -1 ). The electrical conductivity (EC) and oxidation-reduction potential (ORP) of water ranged from 17 to 436 μS·cm -1 and from -52.30 to 674.10 mV, respectively, which were significantly different among the four reaches (P＜0.05). Water ammonium nitrogen (NH 4 + -N) and nitrate nitrogen (NO 3 - -N) concentrations were in the ranges of 0.30-1.35 (averaged 0.90±0.10) mg·L -1 and 0.82-2.45 (averaged 1.62±0.16) mg·L -1 , respectively. The dissolved concentration and diffusion flux of CH 4 ranged from 0 to 5.28 μmol·L -1 and from -0.34 to 619.72 μg C·m -2 ·h -1 , respectively, with significant temporal and spatial variations. They showed a similar trend among reaches. Their values were highest in spring, followed by in winter and lowest in summer and autumn. Spatially, the CH 4 concentration and flux followed the order of S 2 >S 3 >S 4 >S 1 . The correlation analysis showed that CH 4 flux was positively correlated with NH 4 + -N and DOC. The pathway of CH 4 production of all reaches was dominated by acetic acid fermentation, while there were obvious differences among the four reaches. The contribution of CH 4 from acetic acid fermentation was greatest (87%) in S 1 , followed by S 4 (81%), S 2 (78%) and S 3 (76%). The mean value of the δ 13 C for dissolved CH 4 , seston organic matter and benthic organic matter was -41.64‰±1.91‰, -14.07‰±1.06‰ and -26.20‰±1.02‰, respectively. There was a positive correlation between the δ 13 C of dissolved CH 4 and benthic organic matter, whereas the δ 13 C value of dissolved CH 4 was negatively correlated with CH 4 flux.

Ultraviolet absorbance as a proxy for total dissolved mercury in streams

USGS Publications Warehouse

Dittman, J.A.; Shanley, J.B.; Driscoll, C.T.; Aiken, G.R.; Chalmers, A.T.; Towse, J.E.

2009-01-01

Stream water samples were collected over a range of hydrologic and seasonal conditions at three forested watersheds in the northeastern USA. Samples were analyzed for dissolved total mercury (THgd), DOC concentration and DOC composition, and UV254 absorbance across the three sites over different seasons and flow conditions. Pooling data from all sites, we found a strong positive correlation of THgd to DOC (r2 = 0.87), but progressively stronger correlations of THgd with the hydrophobic acid fraction (HPOA) of DOC (r2 = 0.91) and with UV254 absorbance (r2 = 0.92). The strength of the UV254 absorbance-THgd relationship suggests that optical properties associated with dissolved organic matter may be excellent proxies for THgd concentration in these streams. Ease of sample collection and analysis, the potential application of in-situ optical sensors, and the possibility for intensive monitoring over the hydrograph make this an effective, inexpensive approach to estimate THgd flux in drainage waters. ?? 2009 Elsevier Ltd.

Winter to spring variations of chromophoric dissolved organic matter in a temperate estuary (Po River, northern Adriatic Sea).

PubMed

Berto, D; Giani, M; Savelli, F; Centanni, E; Ferrari, C R; Pavoni, B

2010-07-01

The light absorbing fraction of dissolved organic carbon (DOC), known as chromophoric dissolved organic matter (CDOM) showed wide seasonal variations in the temperate estuarine zone in front of the Po River mouth. DOC concentrations increased from winter through spring mainly as a seasonal response to increasing phytoplankton production and thermohaline stratification. The monthly dependence of the CDOM light absorption by salinity and chlorophyll a concentrations was explored. In 2003, neither DOC nor CDOM were linearly correlated with salinity, due to an exceptionally low Po river inflow. Though the CDOM absorbance coefficients showed a higher content of chromophoric dissolved organic matter in 2004 with respect to 2003, the spectroscopic features confirmed that the qualitative nature of CDOM was quite similar in both years. CDOM and DOC underwent a conservative mixing, only after relevant Po river freshets, and a change in optical features with an increase of the specific absorption coefficient was observed, suggesting a prevailing terrestrial origin of dissolved organic matter. Published by Elsevier Ltd.

Switching predominance of organic versus inorganic carbon exports from an intermediate-size subarctic watershed

USGS Publications Warehouse

Dornblaser, Mark M.; Striegl, Robert G.

2015-01-01

Hydrologic exports of dissolved inorganic and organic carbon (DIC, DOC) reflect permafrost conditions in arctic and subarctic river basins. DIC yields in particular, increase with decreased permafrost extent. We investigated the influence of permafrost extent on DIC and DOC yield in a tributary of the Yukon River, where the upper watershed has continuous permafrost and the lower watershed has discontinuous permafrost. Our results indicate that DIC versus DOC predominance switches with interannual changes in water availability and flow routing in intermediate-size watersheds having mixed permafrost coverage. Large water yield and small concentrations from mountainous headwaters and small water yield and high concentrations from lowlands produced similar upstream and downstream carbon yields. However, DOC export exceeded DIC export during high-flow 2011 while DIC predominated during low-flow 2010. The majority of exported carbon derived from near-surface organic sources when landscapes were wet or frozen and from mineralized subsurface sources when infiltration increased.

Sources, behaviors and degradation of dissolved organic matter in the East China Sea

NASA Astrophysics Data System (ADS)

Chen, Yan; Yang, Gui-Peng; Liu, Li; Zhang, Peng-Yan; Leng, Wei-Song

2016-03-01

Concentrations of dissolved organic carbon (DOC), dissolved inorganic nitrogen (DIN), dissolved organic nitrogen (DON) and its major compound classes-total hydrolysable amino acids (THAA) were measured at 4 cross-shelf transects of the East China Sea in July 2011. Surface concentrations of DOC, DIN, DON and THAA at the nearshore stations were mostly in excess of those found at the offshore sites, indicating either substantial autochthonous production or allochthonous inputs from the Changjiang River. The vertical distributions of DOC, DON and THAA showed similar trends with higher values in the surface layer, whereas the elevated concentrations of DIN were observed in the bottom layer. Major constituents of THAA presented in the study area were glycine, serine, alanine, glutamic acid, aspartic acid and valine. The mole percentages of neutral amino acids increased from surface water to bottom water, whereas acidic and hydroxy amino acids decreased with the water depth. Concentrations of DOC and THAA were negatively correlated to the ΔDIN values (the difference between the real concentration and theoretical concentration), respectively, indicating the coupling relation between dissolved organic matter (DOM) remineralization and nutrient regeneration in the water column. The C/N ratios in the water column exhibited different characteristics with elevated values appearing in the surface and bottom layers. Box and whisker plots showed that both degradation index (DI) values and THAA yields displayed a decreasing trend from the surface layer to the bottom layer, implying increasing degradation with the water depth. Our data revealed that glycine and alanine increased in relative abundance with decreasing DI, while tyrosine, valine, phenylalanine and isoleucine increased with increasing DI.

Riverine export of dissolved organic carbon to the Gulf of Maine

NASA Astrophysics Data System (ADS)

Huntington, T. G.; Aiken, G.

2013-12-01

Land-to-sea carbon transport of dissolved organic carbon (DOC) is an important part of the carbon cycle that can affect long-term carbon sequestration, satellite-derived ocean color metrics, and ocean primary productivity and biogeochemistry. Using continuous discharge data and discrete sampling we estimated DOC fluxes from rivers covering about 68% of the watershed that drains to the Gulf of Maine (GoM) for water years (October through September) 2011 and 2012. Estimates for rivers entering the GoM in the USA were made using LOADEST regression software that fits a seasonally-adjusted concentration discharge relation to the data. The basin area-weighted 95% confidence limits about the LOADEST mean fluxes averaged 8.1% for the lower limit and 8.9% for the upper limit. Estimates for rivers entering the GoM in Canada were obtained from previously published estimates. Carbon yield tends to increase from southwest (35 to 36 kg C/ha/yr) to a maximum of 76 kg C/ha/yr for the Penobscot River and then decline further to the northeast (61 kg C/ha/yr in the St. John River and 41 kg C/ha/yr in the rest of New Brunswick and Nova Scotia). The area-weighted average carbon yield for all measured basins was 54.5 kg C/ha/yr. The variation in carbon yield is most closely associated with the amount of runoff and wetland area within a river basin. Simple area-weighted extrapolation to the entire GoM basin resulted in an estimate of 9.8 x 105 metric tons C per year for the WY2011 and WY2012 period. Runoff is the dominant control on intra and inter-annual variation in DOC flux because runoff varies much more than DOC concentration at these temporal scales. Runoff is usually low during the winter, peaks in the spring during snowmelt, decreases to a minimum in late summer and increases again in the fall when transpiration decreases. DOC concentration is low during the winter and snowmelt-dominated spring period, generally increases through the summer, and peaks during the fall. DOC flux to the GoM is characterized by low fluxes in winter, high fluxes during the spring snowmelt and before major increase in transpiration, lower fluxes during summer months and, increasing fluxes in the fall. The increase in spring DOC flux occurs earliest in the major river basins in the southwest and progressively later towards the northeast. Assuming that the seasonally adjusted DOC concentration discharge relationships we obtained have been stable over time we estimated fluxes using historical runoff data to assess potential changes in DOC export from five large river basins with long-term discharge data to the GoM since 1930 (St Croix, Penobscot, Androscoggin, Saco and Merrimack Rivers). DOC export has apparently been increasing over time in association with increasing runoff. The largest increases in DOC in absolute and percentage terms have occurred during October, November, and December. Increases were observed in all months except May when there was a small decrease. The decrease in May and increases in March and April are consistent with earlier snowmelt and earlier onset of transpiration.

Effects of Aftermarket Control Technologies on Gas and Particle Phase Oxidative Potential from Diesel Engine Emissions.

PubMed

Pavlovic, Jelica; Holder, Amara L; Yelverton, Tiffany L B

2015-09-01

Particulate matter (PM) originating from diesel combustion is a public health concern due to its association with adverse effects on respiratory and cardiovascular diseases and lung cancer. This study investigated emissions from three stationary diesel engines (gensets) and varying power output (230 kW, 400 kW, and 600 kW) at 50% and 90% load to determine concentrations of gaseous (GROS) and PM reactive oxygen species (PMROS). In addition, the influence of three modern emission control technologies on ROS emissions was evaluated: active and passive diesel particulate filters (A-DPF and P-DPF) and a diesel oxidation catalyst (DOC). PMROS made up 30-50% of the total ROS measured without aftermarket controls. All applied controls removed PMROS by more than 75% on average. However, the oxidative potential of PM downstream of these devices was not diminished at the same rate and particles surviving the A-PDF had an even higher oxidative potential on a per PM mass basis compared to the particles emitted by uncontrolled gensets. Further, the GROS as compared to PMROS emissions were not reduced with the same efficiency (<36%). GROS concentrations were highest with the DOC in use, indicating continued formation of GROS with this control. Correlation analyses showed that PMROS and to a lesser extent GROS have a good correlation with semivolatile organic carbon (OC1) subfraction. In addition, results suggest that chemical composition, rather than PM size, is responsible for differences in the PM oxidative potential.

Biogeochemical and physical controls on the distribution of dissolved organic carbon in the deep Gulf of Mexico and basins of the Caribbean

NASA Astrophysics Data System (ADS)

Margolin, A. R.; Hansell, D. A.

2016-02-01

Over the past two decades, significant advances have been made in understanding dissolved organic carbon (DOC) distributions in the Atlantic and throughout the global ocean. Surprisingly, however, little is known about DOC distributions in the Atlantic's neighboring Gulf of Mexico (GoM) and Caribbean due to few observations, especially in their deep layers. To address the dearth of DOC data in the GoM and Caribbean, samples were collected during multiple cruises spanning the region, allowing comparisons between the deep layers of the basins. Additionally, complementary biogeochemical (oxygen, nutrients) and physical (temperature, salinity) measurements were made to aid in DOC interpretation, which show clear distinctions between the deep waters of the GoM, basins of the Caribbean and Atlantic. The unique characteristics of these deep layers result from exchanges being restricted to narrow passages that separate the basins, limiting the deep water renewal to periodic overflows of relatively dense water, capable of penetrating below the 2000 m sill depths. Furthermore, hydrocarbon seeps (in GoM) and hydrothermal activity (in Caribbean), along with the offshore oil industry have the potential to alter deep DOC concentrations regionally, which are considered here. Samples collected below 250 m show that concentrations decrease with depth, ranging from 40-50 µmol kg-1. Compared to the Atlantic, the GoM and Venezuelan Basin concentrations are lower, while they are similar to the Atlantic in the Yucatan Basin; responsible processes are inferred.

The removal kinetics of dissolved organic matter and the optical clarity of groundwater

NASA Astrophysics Data System (ADS)

Chapelle, Francis H.; Shen, Yuan; Strom, Eric W.; Benner, Ronald

2016-09-01

Concentrations of dissolved organic matter (DOM) and ultraviolet/visible light absorbance decrease systematically as groundwater moves through the unsaturated zones overlying aquifers and along flowpaths within aquifers. These changes occur over distances of tens of meters (m) implying rapid removal kinetics of the chromophoric DOM that imparts color to groundwater. A one-compartment input-output model was used to derive a differential equation describing the removal of DOM from the dissolved phase due to the combined effects of biodegradation and sorption. The general solution to the equation was parameterized using a 2-year record of dissolved organic carbon (DOC) concentration changes in groundwater at a long-term observation well. Estimated rates of DOC loss were rapid and ranged from 0.093 to 0.21 micromoles per liter per day (μM d-1), and rate constants for DOC removal ranged from 0.0021 to 0.011 per day (d-1). Applying these removal rate constants to an advective-dispersion model illustrates substantial depletion of DOC over flow-path distances of 200 m or less and in timeframes of 2 years or less. These results explain the low to moderate DOC concentrations (20-75 μM; 0.26-1 mg L-1) and ultraviolet absorption coefficient values ( a 254 < 5 m-1) observed in groundwater produced from 59 wells tapping eight different aquifer systems of the United States. The nearly uniform optical clarity of groundwater, therefore, results from similarly rapid DOM-removal kinetics exhibited by geologically and hydrologically dissimilar aquifers.

Origins and bioavailability of dissolved organic matter in groundwater

USGS Publications Warehouse

Shen, Yuan; Chapelle, Francis H.; Strom, Eric W.; Benner, Ronald

2015-01-01

Dissolved organic matter (DOM) in groundwater influences water quality and fuels microbial metabolism, but its origins, bioavailability and chemical composition are poorly understood. The origins and concentrations of dissolved organic carbon (DOC) and bioavailable DOM were monitored during a long-term (2-year) study of groundwater in a fractured-rock aquifer in the Carolina slate belt. Surface precipitation was significantly correlated with groundwater concentrations of DOC, bioavailable DOM and chromophoric DOM, indicating strong hydrological connections between surface and ground waters. The physicochemical and biological processes shaping the concentrations and compositions of DOM during its passage through the soil column to the saturated zone are conceptualized in the regional chromatography model. The model provides a framework for linking hydrology with the processes affecting the transformation, remineralization and microbial production of DOM during passage through the soil column. Lignin-derived phenols were relatively depleted in groundwater DOM indicating substantial removal in the unsaturated zone, and optical properties of chromophoric DOM indicated lower molecular weight DOM in groundwater relative to surface water. The prevalence of glycine, γ-aminobutyric acid, and d-enantiomers of amino acids indicated the DOM was highly diagenetically altered. Bioassay experiments were used to establish DOC-normalized yields of amino acids as molecular indicators of DOM bioavailability in groundwater. A relatively small fraction (8 ± 4 %) of DOC in groundwater was bioavailable. The relatively high yields of specific d-enantiomers of amino acids indicated a substantial fraction (15–34 %) of groundwater DOC was of bacterial origin.

Contrasting composition of terrigenous organic matter in the dissolved, particulate and sedimentary organic carbon pools on the outer East Siberian Arctic Shelf

NASA Astrophysics Data System (ADS)

Salvadó, Joan A.; Tesi, Tommaso; Sundbom, Marcus; Karlsson, Emma; Kruså, Martin; Semiletov, Igor P.; Panova, Elena; Gustafsson, Örjan

2016-11-01

Fluvial discharge and coastal erosion of the permafrost-dominated East Siberian Arctic delivers large quantities of terrigenous organic carbon (Terr-OC) to marine waters. The composition and fate of the remobilized Terr-OC needs to be better constrained as it impacts the potential for a climate-carbon feedback. In the present study, the bulk isotope (δ13C and Δ14C) and macromolecular (lignin-derived phenols) composition of the cross-shelf exported organic carbon (OC) in different marine pools is evaluated. For this purpose, as part of the SWERUS-C3 expedition (July-September 2014), sediment organic carbon (SOC) as well as water column (from surface and near-bottom seawater) dissolved organic carbon (DOC) and particulate organic carbon (POC) samples were collected along the outer shelves of the Kara Sea, Laptev Sea and East Siberian Sea. The results show that the Lena River and the DOC may have a preferential role in the transport of Terr-OC to the outer shelf. DOC concentrations (740-3600 µg L-1) were 1 order of magnitude higher than POC (20-360 µg L-1), with higher concentrations towards the Lena River plume. The δ13C signatures in the three carbon pools varied from -23.9 ± 1.9 ‰ in the SOC, -26.1 ± 1.2 ‰ in the DOC and -27.1 ± 1.9 ‰ in the POC. The Δ14C values ranged between -395 ± 83 (SOC), -226 ± 92 (DOC) and -113 ± 122 ‰ (POC). These stable and radiocarbon isotopes were also different between the Laptev Sea and the East Siberian Sea. Both DOC and POC showed a depleted and younger trend off the Lena River plume. Further, the Pacific inflow and the sea-ice coverage, which works as a barrier preventing the input of "young" DOC and POC, seem to have a strong influence in these carbon pools, presenting older and more enriched δ13C signatures under the sea-ice extent. Lignin phenols exhibited higher OC-normalized concentrations in the SOC (0.10-2.34 mg g-1 OC) and DOC (0.08-2.40 mg g-1 OC) than in the POC (0.03-1.14 mg g-1 OC). The good relationship between lignin and Δ14C signatures in the DOC suggests that a significant fraction of the outer-shelf DOC comes from "young" Terr-OC. By contrast, the slightly negative correlation between lignin phenols and Δ14C signatures in POC, with higher lignin concentrations in older POC from near-bottom waters, may reflect the off-shelf transport of OC from remobilized permafrost in the nepheloid layer. Syringyl / vanillyl and cinnamyl / vannillyl phenol ratios presented distinct clustering between DOC, POC and SOC, implying that those pools may be carrying different Terr-OC of partially different origin. Moreover, 3,5-dihydroxybenzoic acid to vanillyl phenol ratios and p-coumaric acid to ferulic acid ratios, used as a diagenetic indicators, enhanced in POC and SOC, suggesting more degradation within these pools. Overall, the key contrast between enhanced lignin yields both in the youngest DOC and the oldest POC samples reflects a significant decoupling of terrestrial OC sources and pathways.

Simultaneous effect of dissolved organic carbon, surfactant, and organic acid on the desorption of pesticides investigated by response surface methodology.

PubMed

Trinh, Ha Thu; Duong, Hanh Thi; Ta, Thao Thi; Van Cao, Hoang; Strobel, Bjarne W; Le, Giang Truong

2017-08-01

Desorption of pesticides (fenobucarb, endosulfan, and dichlorodiphenyltrichloroethane (DDT)) from soil to aqueous solution with the simultaneous presence of dissolved organic carbon (DOC), sodium dodecyl sulfate (SDS), and sodium oxalate (Oxa) was investigated in batch test by applying a full factorial design and the Box-Behnken response surface methodology (RSM). Five concentration levels of DOC (8 to 92 mg L -1 ), SDS (0 to 6.4 critical micelle concentration (CMC)), and Oxa (0 to 0.15 M) were used for the experiments with a rice field topsoil. The results of RSM analysis and analysis of variance (ANOVA) have shown that the experimental data could be well described by quadratic regression equations with determination coefficients (R 2 ) of 0.990, 0.976, and 0.984 for desorption of fenobucarb, endosulfan, and DDT, respectively. The individual effects and interaction of DOC, SDS, and Oxa were evaluated through quadratic regression equations. When the aqueous solution includes 50 mg L -1 DOC, 3.75 CMC SDS, and 0.1 M Oxa, the maximum desorption concentrations of fenobucarb, endosulfan, and DDT were 96, 80, and 75 μg L -1 , respectively. The lowest concentration of SDS, DOC, and Oxa caused the minimum desorption. This point at conditions of concern for flooding water is high content of organic compounds causing potentially high contamination by desorption, and the remarkably lower desorption at organic matter-free conditions. The suspended organic matter is one of the common characteristics of flooding and irrigation water in rice fields, and surfactants from pollution increase the problem with desorption of legacy pesticides in the rice fields.

Influence of indian mustard (Brassica juncea) on rhizosphere soil solution chemistry in long-term contaminated soils: a rhizobox study.

PubMed

Kim, Kwon-Rae; Owens, Gary; Kwon, Soon-lk

2010-01-01

This study investigated the influence of Indian mustard (Brassica juncea) root exudation on soil solution properties (pH, dissolved organic carbon (DOC), metal solubility) in the rhizosphere using a rhizobox. Measurement was conducted following the cultivation of Indian mustard in the rhizobox filled four different types of heavy metal contaminated soils (two alkaline soils and two acidic soils). The growth of Indian mustard resulted in a significant increase (by 0.6 pH units) in rhizosphere soil solution pH of acidic soils and only a slight increase (< 0.1 pH units) in alkaline soils. Furthermore, the DOC concentration increased by 17-156 mg/L in the rhizosphere regardless of soil type and the extent of contamination, demonstrating the exudation of DOC from root. Ion chromatographic determination showed a marked increase in the total dissolved organic acids (OAs) in rhizosphere. While root exudates were observed in all soils, the amount of DOC and OAs in soil solution varied considerably amongst different soils, resulting in significant changes to soil solution metals in the rhizosphere. For example, the soil solution Cd, Cu, Pb, and Zn concentrations increased in the rhizosphere of alkaline soils compared to bulk soil following plant cultivation. In contrast, the soluble concentrations of Cd, Pb, and Zn in acidic soils decreased in rhizosphere soil when compared to bulk soils. Besides the influence of pH and DOC on metal solubility, the increase of heavy metal concentration having high stability constant such as Cu and Pb resulted in a release of Cd and Zn from solid phase to liquid phase.

The effect of feed water dissolved organic carbon concentration and composition on organic micropollutant removal and microbial diversity in soil columns simulating river bank filtration.

PubMed

Bertelkamp, C; van der Hoek, J P; Schoutteten, K; Hulpiau, L; Vanhaecke, L; Vanden Bussche, J; Cabo, A J; Callewaert, C; Boon, N; Löwenberg, J; Singhal, N; Verliefde, A R D

2016-02-01

This study investigated organic micropollutant (OMP) biodegradation rates in laboratory-scale soil columns simulating river bank filtration (RBF) processes. The dosed OMP mixture consisted of 11 pharmaceuticals, 6 herbicides, 2 insecticides and 1 solvent. Columns were filled with soil from a RBF site and were fed with four different organic carbon fractions (hydrophilic, hydrophobic, transphilic and river water organic matter (RWOM)). Additionally, the effect of a short-term OMP/dissolved organic carbon (DOC) shock-load (e.g. quadrupling the OMP concentrations and doubling the DOC concentration) on OMP biodegradation rates was investigated to assess the resilience of RBF systems. The results obtained in this study imply that - in contrast to what is observed for managed aquifer recharge systems operating on wastewater effluent - OMP biodegradation rates are not affected by the type of organic carbon fraction fed to the soil column, in case of stable operation. No effect of a short-term DOC shock-load on OMP biodegradation rates between the different organic carbon fractions was observed. This means that the RBF site simulated in this study is resilient towards transient higher DOC concentrations in the river water. However, a temporary OMP shock-load affected OMP biodegradation rates observed for the columns fed with the river water organic matter (RWOM) and the hydrophilic fraction of the river water organic matter. These different biodegradation rates did not correlate with any of the parameters investigated in this study (cellular adenosine triphosphate (cATP), DOC removal, specific ultraviolet absorbance (SUVA), richness/evenness of the soil microbial population or OMP category (hydrophobicity/charge). Copyright © 2015 Elsevier Ltd. All rights reserved.

Watershed scale spatial variability in dissolved and total organic and inorganic carbon in contrasting UK catchments

NASA Astrophysics Data System (ADS)

Cumberland, S.; Baker, A.; Hudson, N. J.

2006-12-01

Approximately 800 organic and inorganic carbon analyses have been undertaken from watershed scale and regional scale spatial surveys in various British catchments. These include (1) a small (<100 sq-km) urban catchment (Ouseburn, N England); (2) a headwater, lowland agricultural catchment (River Tern, C England) (3) a large UK catchment (River Tyne, ~3000 sq-km) and (4) a spatial survey of ~300 analyses from rivers from SW England (~1700 sq-km). Results demonstrate that: (1) the majority of organic and inorganic carbon is in the dissolved (DOC and DIC) fractions; (2) that with the exception of peat rich headwaters, DIC concentration is always greater than DOC; (3) In the rural River Tern, riverine DOC and DIC are shown to follow a simple end- member mixing between DIC (DOC) rich (poor) ground waters and DOC (DIC) rich (poor) riparian wetlands for all sample sites. (4) In the urbanized Ouseburn catchment, although many sample sites also show this same mixing trend, some tributaries follow a pollutant trend of simultaneous increases in both DOC and DIC. The Ouseburn is part of the larger Tyne catchment: this larger catchment follows the simple groundwater DIC- soil water DOC end member mixing model, with the exception of the urban catchments which exhibit an elevated DIC compared to rural sites. (5) Urbanization is demonstrated to increase DIC compared to equivalent rural catchments; this DIC has potential sources including diffuse source inputs from the dissolution of concrete, point sources such as trade effluents and landfill leachates, and bedrock derived carbonates relocated to the soil dissolution zone by urban development. (6) DIC in rural SW England demonstrates that spatial variability in DIC can be attributed to variations in geology; but that DIC concentrations in the SW England rivers dataset are typically lower than the urbanized Tyne catchments despite the presence of carbonate bedrock in many of the sample catchments in the SW England dataset. (7) Recent investigations into carbon fluxes in British rivers have focused on long term increases in DOC in rural and predominantly upland catchments. Our results suggest that research is needed into understanding long term variations in inorganic carbon concentration, as well as total (organic and inorganic) carbon fluxes from British rivers, to obtain total carbon loads. In particular, we provide evidence that DIC concentrations may be greater in urbanized catchments compared to equivalent non-urban catchments, with the implication that increasing urbanization in the future will see increases in riverine DIC and a decrease in the strength of any DOC DIC anti correlation. Further studies of urban catchment DIC sources, within stream processing, long term trends, and potential ecological impacts, are required.

The relationship between soil heterotrophic activity, soil dissolved organic carbon (DOC) leachate, and catchment-scale DOC export in headwater catchments

USGS Publications Warehouse

Brooks, P.D.; McKnight, Diane M.; Bencala, K.E.

1999-01-01

Dissolved organic carbon (DOC) from terrestrial sources forms the major component of the annual carbon budget in many headwater streams. In high-elevation catchments in the Rocky Mountains, DOC originates in the upper soil horizons and is flushed to the stream primarily during spring snowmelt. To identify controls on the size of the mobile soil DOC pool available to be transported during the annual melt event, we measured soil DOC production across a range of vegetation communities and soil types together with catchment DOC export in paired watersheds in Summit County, Colorado. Both surface water DOC concentrations and watershed DOC export were lower in areas where pyrite weathering resulted in lower soil pH. Similarly, the amount of DOC leached from organic soils was significantly smaller (p < 0.01) at sites having low soil pH. Scaling point source measurements of DOC production and leaching to the two basins and assuming only vegetated areas contribute to DOC production, we calculated that the amount of mobile DOC available to be leached to surface water during melt was 20.3 g C m−2 in the circumneutral basin and 17.8 g C m−2 in the catchment characterized by pyrite weathering. The significant (r2=0.91 and p < 0.05), linear relationship between over-winter CO2 flux and the amount of DOC leached from upper soil horizons during snowmelt suggests that the mechanism for the difference in production of mobile DOC was heterotrophic processing of soil carbon in snow-covered soil. Furthermore, this strong relationship between over-winter heterotrophic activity and the size of the mobile DOC pool present in a range of soil and vegetation types provides a likely mechanism for explaining the interannual variability of DOC export observed in high-elevation catchments.

Contrasting dissolved organic carbon dynamics at two forested catchments interpreted from high-frequency optical sensor measurements

NASA Astrophysics Data System (ADS)

Saraceno, J.; Shanley, J. B.

2015-12-01

Stream dissolved organic carbon (DOC) concentrations can change rapidly during high-flow events. The timing and magnitude of these changes relative to the event hydrograph can yield insights about possible DOC sources its flow paths to the stream. In situ fluorescent dissolved organic matter (FDOM) sensors that generate high-frequency observations enable detailed examination of high-flow DOC- discharge hysteresis. In this presentation, we interpret high-flow DOC dynamics at two of the five U.S. Geological Survey (USGS) Water, Energy, and Biogeochemical Budgets (WEBB) sites - Panola Mountain, Georgia and Sleepers River, Vermont. Based on laboratory analyses of weekly and event grab samples, both USGS WEBB sites had a similar DOC ranges: from ~1 milligrams per liter (mg/L) at base flow to ~11-15 mg/L during the largest events. A curvilinear relationship between DOC and FDOM (corrected for temperature and turbidity interferences) was used to model a continuous time series of DOC. At the Sleepers River site, DOC showed a seasonal pattern of increasing DOC response; from fairly subdued during spring snowmelt, to a maximum during autumn leaf-fall. The DOC response to discharge showed a consistent clockwise hysteresis (DOC peak, lagged discharge peak). At the Panola Mountain site, maximum event DOC response was lower during wet conditions in the winter and spring. Hysteresis was less expressed at Panola Mountain relative to Sleepers River and displayed both clockwise and counterclockwise patterns, which were dependent on antecedent moisture conditions. The greater synchrony of DOC and discharge peaks at Panola Mountain suggests that DOC sources are closer to the stream and (or) move to the stream more quickly, than at Sleepers River.

The use of carbon adsorbents for the removal of perfluoroalkyl acids from potable reuse systems.

PubMed

Inyang, Mandu; Dickenson, Eric R V

2017-10-01

Bench- and pilot-scale sorption tests were used to probe the performance of several biochars at removing perfluoroalkyl acids (PFAA) from field waters, compared to granular activated carbon (GAC). Screening tests using organic matter-free water resulted in hardwood (HWC) (K d  = 41 L g -1 ) and pinewood (PWC) (K d  = 49 L g -1 ) biochars having the highest perfluorooctanoic acid (PFOA) removal performance that was comparable to bituminous coal GAC (K d  = 41 L g -1 ). PWC and HWC had a stronger affinity for PFOA sorbed in Lake Mead surface water (K F  = 11 mg (1-n) L n g -1 ) containing a lower (2 mg L -1 ) dissolved organic carbon (DOC) concentration than in a tertiary-filtered wastewater (K F  = 8 mg (1-n) L n g -1 ) with DOC of 4.9 mg L -1 . A pilot-scale study was performed using three parallel adsorbers (GAC, anthracite, and HWC biochar) treating the same tertiary-filtered wastewater. Compared to HWC, and anthracite, GAC was the most effective in mitigating perfluoropentanoic acid (PFPnA), perfluorohexanoic acid (PHxA), PFOA, perfluorooctane sulfonic acid (PFOS), and DOC (45-67% removed at 4354 bed volumes) followed by HWC, and then anthracite. Based on bench- and pilot-scale results, shorter-chain PFAA [perfluorobutanoic acid (PFBA), PFPnA, or PFHxA] were more difficult to remove with both biochar and GAC than the longer-chain, PFOS and PFOA. Copyright © 2017 Elsevier Ltd. All rights reserved.

Laboratory investigations into the potential for transformation of POC to dissolved and gaseous forms

NASA Astrophysics Data System (ADS)

Goulsbra, Claire; Evans, Martin; Allott, Tim; Evans, Chris; Flint, Rebecca; Mcmorron, Katherine

2014-05-01

In eroding peatland systems POC is the dominant component of the fluvial carbon flux, with POC flux to up to circa 80 g C m-2 yr-1. The fate of this POC has remained uncertain, however, and at present many carbon models exclude POC flux from estimations of atmospherically active carbon budgets. Recent work on headwater systems with high POC concentrations has demonstrated that POC:DOC ratios decrease rapidly downstream, hypothesised to be due the physical and microbial breakdown of POC in the fluvial system and transformation of soil carbon to dissolved and gaseous phases. To assess this hypothesis, laboratory investigations of the potential for transformation of POC to dissolved and gaseous forms were undertaken. POC derived from an exposed gully face was mixed with stream waters collected from Upper North Grain, an eroded peatland catchment in the South Pennines, UK, to simulate typical storm flow suspended sediment concentrations. The solutions were agitated using a magnetic stirring system for one week and subsamples of the solution were extracted at intervals of 0.5, 1, 1.5, 2, 3, 4, 5 and 6 hours, and 1, 2, 3, 4, and 7 days. Samples were analysed for POC and DOC concentration using a Shimadzu total carbon analyser and absorbance was measured spectrophotometrically at 254, 400 465 and 665 nm wavelengths as a proxy for DOC quality. In a parallel experiment CO2 emissions to the mixing flask were measured using an infra-red gas analyser (IRGA). To isolate the role of microbial versus physical breakdown, both experiments were replicated with POM and streamwater which had been sterilised by gamma irradiation. The experiments were further repeated to assess the impact of variations in pH and the initial DOC concentration of the stream water on rates of POC conversion to on DOC and CO2. The results of these experiments will be presented here. Initial results show that peat-derived POC was found to be reactive in streamwater, leading to a rapid in DOC within 24 hours of the start of mixing experiments, thought to occur via physicochemical processes. Mixing of POC with streamwater also led to rapid CO2 emissions, possibly via a DOC intermediary, and overall CO2 production exceeded that of DOC. These results strongly indicate that POC is actively converted to other carbon forms in high-POC waters over the timescale of water residence in typical UK river systems, and that a high proportion of this carbon is emitted to the atmosphere as CO2.

Controls on accumulation and soil solution partitioning of heavy metals across upland sites in United Kingdom (UK).

PubMed

Zia, Afia; van den Berg, Leon; Ahmad, Muhammad Nauman; Riaz, Muhammad; Zia, Dania; Ashmore, Mike

2018-05-31

A significant body of knowledge suggests that soil solution pH and dissolved organic carbon (DOC) strongly influence metal concentrations and speciation in porewater, however, these effects vary between different metals. This study investigated the factors influencing soil and soil solution concentrations of copper (Cu), lead (Pb), nickel (Ni) and zinc (Zn) under field conditions in upland soils from UK having a wide range of pH, DOC and organic matter contents. The study primarily focussed on predicting soil and soil solution metal concentrations from the data on total soil metal concentrations (HNO 3 extracts) and soil and soil solution properties (pH, DOC and organic matter content). We tested the multiple regression models proposed by Tipping et al. (2003) to predict heavy metal concentrations in soil solutions and the results indicated a better fit (higher R 2 values) in both studies for Pb compared to the Zn and Cu concentrations. Both studies observed consistent negative relationships of metals with pH and loss on ignition (LOI) suggesting an increase in soil solution metal concentrations with increasing acidity. The positive relationship between Pb concentrations in porewater and HNO 3 extracts was similar for both studies, however, similar relationships were not found for the Zn and Cu concentrations because of the negative coefficients for these metals in our study. The results of this study conclude that the predictive equations of Tipping et al. (2003) may not be applicable to the field sites where the range of DOC and metal concentrations is much lower than their study. Our study also suggests that the extent to which metals are partitioned into soil solution is lower in soils with a higher organic matter contents due to binding of these metals to soil organic matter. Copyright © 2018 Elsevier Ltd. All rights reserved.

Dissolved organic carbon biodegradability from leaf litter leachates of riparian tropical trees

NASA Astrophysics Data System (ADS)

Bastianoni, A.; Montoya, J. V.; Mendez, C.; Paolini, J.

2012-04-01

It is generally assumed that leaf litter with varying chemical composition may show different rates of mass loss, dissolved organic carbon (DOC) release, and DOC biodegradability. Leaf litter is composed of different organic compounds, which may differ in their release rates. Some authors consider leaf litter chemical quality (carbon to nitrogen ratio (C:N) and polyphenolics content) as an indicator of leaf litter mass losses and DOC released into stream water through leaching. In this research, we determined if leachate's DOC biodegradability exhibited a positive relationship with leaf litter chemical quality and leaf litter mass loss due to leaching. In order to test these hypotheses, leaf litter from six riparian tree species (Bambusa vulgaris; Castilla elastica; Artocarpus altilis; Cecropia peltata; Hura crepitans and Ficus maxima), present in the lower reaches of a fifth-order stream in northern Venezuela was collected during the dry season of 2010. To evaluate leaf litter mass loss, air-dried leaves were incubated in Milli-Q water at room temperature in the dark. After 1h, 6h, 1d, 2d, 4d, 8d and 15d, microcosms were removed from the assay to determine remaining mass. DOC biodegradability was measured using 24 h leachates that were added into a 1L glass flask containing 250mL of unfiltered stream water, 4g of stream sediment, and nutrient amendments until all incubations had equal initial DOC concentrations. Biodegradability of DOC was measured at 0, 1, 2, 5 and 7 days as the decrease in DOC concentration through time. Chemical characterization of leaf litter involved the determination of total concentrations of C, N, and poliphenolics. Three replicates were used for all analyses. Initial chemical characterization of leaf litter showed that only two species (C. elastica and A. altilis), had similar C:N ratios (~31). The other four species, showed different C and N contents but presented C:N ratios between 21 and 23. Total polyphenolics content varied greatly among species. Based on the degree of DOC biodegradability, after 1d of incubation, all species could be grouped into three distinct categories (high, intermediate and low). Then, biodegradability of DOC declined steadily until reaching near-constant values at day 7 probably reflecting less availability of labile C compounds. Breakdown rates were not significantly correlated with DOC decay rates (r=-0.580, P =0.228, n=6). However when the remaining DOC and the remaining mass for all species was evaluated, a significant negative correlation was observed (r=-0.567, P =0.014, n=18) contradicting our initial hypothesis. Such results might be a consequence of the presence of secondary metabolites alongside labile DOC in some species leachates which could prevent microbial C consumption. Therefore, the quality of C released by leaching, measured as its biodegradability, does not seem to have a relationship with the amount of C lost by leaching. This could influence the C budget of the riparian ecosystem since the proportion of C consumed by stream microbes is affected by the chemical quality of leaf litter leachates.

Hidden cycle of dissolved organic carbon in the deep ocean.

PubMed

Follett, Christopher L; Repeta, Daniel J; Rothman, Daniel H; Xu, Li; Santinelli, Chiara

2014-11-25

Marine dissolved organic carbon (DOC) is a large (660 Pg C) reactive carbon reservoir that mediates the oceanic microbial food web and interacts with climate on both short and long timescales. Carbon isotopic content provides information on the DOC source via δ(13)C and age via Δ(14)C. Bulk isotope measurements suggest a microbially sourced DOC reservoir with two distinct components of differing radiocarbon age. However, such measurements cannot determine internal dynamics and fluxes. Here we analyze serial oxidation experiments to quantify the isotopic diversity of DOC at an oligotrophic site in the central Pacific Ocean. Our results show diversity in both stable and radio isotopes at all depths, confirming DOC cycling hidden within bulk analyses. We confirm the presence of isotopically enriched, modern DOC cocycling with an isotopically depleted older fraction in the upper ocean. However, our results show that up to 30% of the deep DOC reservoir is modern and supported by a 1 Pg/y carbon flux, which is 10 times higher than inferred from bulk isotope measurements. Isotopically depleted material turns over at an apparent time scale of 30,000 y, which is far slower than indicated by bulk isotope measurements. These results are consistent with global DOC measurements and explain both the fluctuations in deep DOC concentration and the anomalous radiocarbon values of DOC in the Southern Ocean. Collectively these results provide an unprecedented view of the ways in which DOC moves through the marine carbon cycle.

Hidden cycle of dissolved organic carbon in the deep ocean

PubMed Central

Follett, Christopher L.; Repeta, Daniel J.; Rothman, Daniel H.; Xu, Li; Santinelli, Chiara

2014-01-01

Marine dissolved organic carbon (DOC) is a large (660 Pg C) reactive carbon reservoir that mediates the oceanic microbial food web and interacts with climate on both short and long timescales. Carbon isotopic content provides information on the DOC source via δ13C and age via Δ14C. Bulk isotope measurements suggest a microbially sourced DOC reservoir with two distinct components of differing radiocarbon age. However, such measurements cannot determine internal dynamics and fluxes. Here we analyze serial oxidation experiments to quantify the isotopic diversity of DOC at an oligotrophic site in the central Pacific Ocean. Our results show diversity in both stable and radio isotopes at all depths, confirming DOC cycling hidden within bulk analyses. We confirm the presence of isotopically enriched, modern DOC cocycling with an isotopically depleted older fraction in the upper ocean. However, our results show that up to 30% of the deep DOC reservoir is modern and supported by a 1 Pg/y carbon flux, which is 10 times higher than inferred from bulk isotope measurements. Isotopically depleted material turns over at an apparent time scale of 30,000 y, which is far slower than indicated by bulk isotope measurements. These results are consistent with global DOC measurements and explain both the fluctuations in deep DOC concentration and the anomalous radiocarbon values of DOC in the Southern Ocean. Collectively these results provide an unprecedented view of the ways in which DOC moves through the marine carbon cycle. PMID:25385632

Concentration and characterization of dissolved organic matter in the surface microlayer and subsurface water of the Bohai Sea, China

NASA Astrophysics Data System (ADS)

Chen, Yan; Yang, Gui-Peng; Wu, Guan-Wei; Gao, Xian-Chi; Xia, Qing-Yan

2013-01-01

A total of 19 sea-surface microlayer and corresponding subsurface samples collected from the Bohai Sea, China in April 2010 were analyzed for chlorophyll a, dissolved organic carbon (DOC) and its major compound classes including total dissolved carbohydrates (TDCHO, including monosaccharides, MCHO, and polysaccharides, PCHO) and total hydrolysable amino acids (THAA, including dissolved free, DFAA, and combined fraction, DCAA). The concentrations of DOC in the subsurface water ranged from 130.2 to 407.7 μM C, with an average of 225.9±75.4 μM C, while those in the surface microlayer varied between 140.1 and 330.9 μM C, with an average of 217.8±56.8 μM C. The concentrations of chlorophyll a, DOC, TDCHO and THAA in the microlayer were, respectively correlated with their subsurface water concentrations, implying that there was a strong exchange effect between the microlayer and subsurface water. The concentrations of DOC and TDCHO were negatively correlated with salinity, respectively, indicating that water mixing might play an important role in controlling the distribution of DOC and TDCHO in the water column. Major constituents of DCAA and DFAA present in the study area were glycine, alanine, glutamic acid, serine and histidine. Principal component analysis (PCA) was applied to examine the complex compositional differences that existed among the sampling sites. Our results showed that DFAA had higher mole percentages of glycine, valine and serine in the microlayer than in the subsurface water, while DCAA tended to have higher mole percentages of glutamic acid, aspartic acid, threonine, arginine, alanine, tyrosine, phenylalanine and leucine in the microlayer. The yields of TDCHO and THAA exhibited similar trends between the microlayer and subsurface water. Carbohydrate species displayed significant enrichment in the microlayer, whereas the DFAA and DCAA exhibited non-uniform enrichment in the microlayer.

Photooxidation and Microbial Processing of Ancient and Modern Dissolved Organic Carbon in the Kolyma River, Siberia.

NASA Astrophysics Data System (ADS)

Behnke, M. I.; Mann, P. J.; Schade, J. D.; Spawn, S.; Zimov, N.

2015-12-01

Permafrost soils in northern high latitudes store large quantities of organic carbon that have remained frozen for thousands of years. As global temperatures increase, permafrost deposits have begun to thaw, releasing previously stored ancient carbon to streams and rivers in the form of dissolved organic carbon (DOC). Newly mobilized DOC is then subjected to processing by photooxidation and microbial metabolism. Permafrost-derived DOC is highly bioavailable directly upon release relative to modern DOC derived from plants and surface active layer soils. Our objectives were to assess the interaction of photodegradation and microbial processing, and to quantify any light priming effect on the microbial consumption of both ancient and modern sourced DOC pools. We exposed sterilized mixtures of ancient and modern DOC to ambient sunlight for six days, and then inoculated mixtures (0, 1, 10, 25, 50 & 100% ancient DOC) with microbes from both modern and ancient water sources. After inoculation, samples were incubated in the dark for five days. We measured biological oxygen demand, changes in absorbance, and DOC concentrations to quantify microbial consumption of DOC and identify shifts in DOC composition and biolability. We found evidence of photobleaching during irradiation (decreasing S275-295, increasing slope ratio, and decreasing SUVA254). Once inoculated, mixtures with more ancient DOC showed initially increased microbial respiration compared to mixtures with primarily modern DOC. During the first 24 hours, the light-exposed mixture with 50% ancient DOC showed 47.6% more oxygen consumption than did the dark 50% mixture, while the purely modern DOC showed 11.5% greater oxygen consumption after light exposure. After 5 days, the modern light priming was comparable to the 50% mixture (31.2% compared to 20.5%, respectively). Our results indicate that natural photoexposure of both modern and newly released DOC increases microbial processing rates over non photo-exposed DOC.

Water Soluble Organic Compounds over the Eastern Mediterranean: Study of their occurrence and sources

NASA Astrophysics Data System (ADS)

Tziaras, T.; Spyros, A.; Mandalakis, M.; Apostolaki, M.; Stephanou, E. G.

2010-05-01

Fine marine aerosols influence the climate system by acting as cloud condensation nuclei (CCN) in the atmosphere. The organic chemical composition and origin of the marine fine particulate matter are still largely unknown, because of the insufficient reports on in situ studies, the large variability in the emission from the sea, from the complex transfer of gases and particles at the air-sea interface, and the transport of aerosol particles from very distant sources. As important processes of formation of marine organic aerosol production we consider: transport of terrestrial particles, secondary organic aerosol (SOA) formation from the oxidation of biogenic dimethyl-sulfide (DMS), and biogenic particle emissions through sea spray. Specific compounds related to the above-mentioned processes have been proposed as molecular markers: e.g. n-alkanoic acids and n-alkanes (terrestrial particles), levoglucosan (biomass burning aerosol), aminoacids (biological terrestrial or marine particles), methanesulphonate (MSA) (DMS oxidation), C8 and C9 dicarboxylic acids and oxo-carboxylic acids (marine SOA) and other short-chain dicarboxylic acids (marine or terrestrial SOA), and humic-like compounds (emission of marine organic carbon). In our study, we made an effort to characterize the water-soluble organic fraction of marine aerosols collected at a background sampling site of Eastern Mediterranean (Finokalia, N35o20', E25o40', Island of Crete, Greece). The sampling period was 2007-2008. In order to identify and quantify the water-soluble organic compounds of marine aerosols determined in the present study we have used gas chromatography/mass spectrometry (GC/MS), liquid chromatography/mass spectrometry (LC/MS) and nuclear magnetic resonance spectroscopy (NMR) and ion chromatography (IC). The origin of air masses arriving in the study area was studied by using backward trajectories calculation (NOAA HYSPLIT Model). In addition, we have used the "MODIS fire products" for fire detects. The sampling period was 2007-2008. Measurements of collective parameters such as organic/elemental carbon (OC/EC), dissolved organic carbon (DOC), and aerosol surface active substances as methylene blue active substances (MBAS) were also performed. The concentration ranges for total suspended particles (TSP) was 12.3-61.1 microg m-3, for OC and EC 0.6-2.2 microg m-3 and 0.1-0.4 microg m-3 respectively, for DOC 0.7-1.8 microg m-3, and for MBAS 7.4-15.4 ng m-3. The average ratio OC/EC was 6.9 (+/- 3.5) and the proportion of DCO in relation to OC was 83 (+/-13) %, indicating a high degree of oxidation in the water-soluble organic matter. OC and DOC were statistically strongly correlated with the intensity of fire events in southern Europe. The analysis of the water soluble organic extract by GC/MS, NMR and revealed the presence of 130 individual organic compounds which made the 17% of DOC. The most significant categories were: I) Twenty (20) amino acids were determined as free (FAA) and combined (CAA) amino acids with an average concentration of 16 and 66 ng m-3 respectively. The average concentration of total amino acids (TAA) was 82 ng m-3. Glycine, glutamine, glutamic acid, aspartic acid and alanine made the 87% of the FAA fraction and glycine, alanine, glutamic acid, aspartic acid, valine and leucine the 87% of CAA. Statistically significant correlations were found between FAA and CAA, and MBAS and the intensity of fire events. II) Twenty six (26) n-alkanoic acids (C2-C14) were detected with an average concentration of 145 ng m-3. Acetic acid, tridecanoic and heneicosanoic acids demonstrated the highest correlation with fire events. III) Twenty two (22) saturated, unsaturated and branched dicarboxylic acids were analysed with an average concentration of 526 ng m-3. The highest statistical correlation with fire events was determined for the concentration of dicarboxylic acids with Cn larger than 6. IV) Thirty one (31) hydroxy-, oxo- and keto- carboxylic and dicarboxylic acids were also determined. Their average concentration was 126 ng m-3. The most significant statistical correlation with fire events were determined for the concentration of glycolic acid and keto-octanoic acid. V) Various aromatic aromatic acids and polycarboxylic acids, such as 4-hydroxy-benzoic acid, syringic acid and trans-7-carbomethoxy-2-octendioic acid have shown the highest concentration correlation with fire events. VI) Pinic and pinonic acids were present in relatively low concentrations (ca. 3 ng m-3). It is interesting that organosulfates of these acids were determined in the Eastern Mediterranean marine aerosol by using LC/MS. Our results show that fire events (biomass burning) in southern Europe is a major source of water-soluble oxygenated organic compounds in the marine atmosphere. The concurrent use of mass spectrometry and NMR techniques allowed a better determination of the organic content of marine aerosols.

Hydrological controls on DOC  :  nitrate resource stoichiometry in a lowland, agricultural catchment, southern UK

NASA Astrophysics Data System (ADS)

Heppell, Catherine M.; Binley, Andrew; Trimmer, Mark; Darch, Tegan; Jones, Ashley; Malone, Ed; Collins, Adrian L.; Johnes, Penny J.; Freer, Jim E.; Lloyd, Charlotte E. M.

2017-09-01

The role that hydrology plays in governing the interactions between dissolved organic carbon (DOC) and nitrogen in rivers draining lowland, agricultural landscapes is currently poorly understood. In light of the potential changes to the production and delivery of DOC and nitrate to rivers arising from climate change and land use management, there is a pressing need to improve our understanding of hydrological controls on DOC and nitrate dynamics in such catchments. We measured DOC and nitrate concentrations in river water of six reaches of the lowland river Hampshire Avon (Wiltshire, southern UK) in order to quantify the relationship between BFI (BFI) and DOC : nitrate molar ratios across contrasting geologies (Chalk, Greensand, and clay). We found a significant positive relationship between nitrate and BFI (p < 0. 0001), and a significant negative relationship between DOC and BFI (p < 0. 0001), resulting in a non-linear negative correlation between DOC : nitrate molar ratio and BFI. In the Hampshire Avon, headwater reaches which are underlain by clay and characterized by a more flashy hydrological regime are associated with DOC : nitrate ratios > 5 throughout the year, whilst groundwater-dominated reaches underlain by Chalk, with a high BFI have DOC : nitrate ratios in surface waters that are an order of magnitude lower (< 0.5). Our analysis also reveals significant seasonal variations in DOC : nitrate transport and highlights critical periods of nitrate export (e.g. winter in sub-catchments underlain by Chalk and Greensand, and autumn in drained, clay sub-catchments) when DOC : nitrate molar ratios are low, suggesting low potential for in-stream uptake of inorganic forms of nitrogen. Consequently, our study emphasizes the tight relationship between DOC and nitrate availability in agricultural catchments, and further reveals that this relationship is controlled to a great extent by the hydrological setting.

Changes in the chemistry of acidified Adirondack streams from the early 1980s to 2008

USGS Publications Warehouse

Lawrence, G.B.; Simonin, H.A.; Baldigo, Barry P.; Roy, K.M.; Capone, S.B.

2011-01-01

Lakes in the Adirondack region of New York have partially recovered in response to declining deposition, but information on stream recovery is limited. Here we report results of Adirondack stream monitoring from the early 1980s to 2008. Despite a 50% reduction in atmospheric deposition of sulfur, overall increases in pH of only 0.28 and ANC of 13 μeq L-1 were observed in 12 streams over 23 years, although greater changes did occur in streams with lower initial ANC, as expected. In the North Tributary of Buck Creek with high dissolved organic carbon (DOC) concentrations, SO(4)(2-) concentrations decreased from 1999 to 2008 at a rate of 2.0 μmol L-1 y-1, whereas in the neighboring South Tributary with low DOC concentrations, the decrease was only 0.73 μmol L-1 y-1. Ca2+ leaching decreased in the North Tributary due to the SO(4)(2-) decrease, but this was partially offset by an increase in Ca2+ leaching from increased DOC concentrations.

Assessment of potential climate change impacts on peatland dissolved organic carbon release and drinking water treatment from laboratory experiments.

PubMed

Tang, R; Clark, J M; Bond, T; Graham, N; Hughes, D; Freeman, C

2013-02-01

Catchments draining peat soils provide the majority of drinking water in the UK. Over the past decades, concentrations of dissolved organic carbon (DOC) have increased in surface waters. Residual DOC can cause harmful carcinogenic disinfection by-products to form during water treatment processes. Increased frequency and severity of droughts combined with and increased temperatures expected as the climate changes, have potentials to change water quality. We used a novel approach to investigate links between climate change, DOC release and subsequent effects on drinking water treatment. We designed a climate manipulation experiment to simulate projected climate changes and monitored releases from peat soil and litter, then simulated coagulation used in water treatment. We showed that the 'drought' simulation was the dominant factor altering DOC release and affected the ability to remove DOC. Our results imply that future short-term drought events could have a greater impact than increased temperature on DOC treatability. Copyright © 2012 Elsevier Ltd. All rights reserved.

First dynamic model of dissolved organic carbon derived directly from high-frequency observations through contiguous storms.

PubMed

Jones, Timothy D; Chappell, Nick A; Tych, Wlodek

2014-11-18

The first dynamic model of dissolved organic carbon (DOC) export in streams derived directly from high frequency (subhourly) observations sampled at a regular interval through contiguous storms is presented. The optimal model, identified using the recently developed RIVC algorithm, captured the rapid dynamics of DOC load from 15 min monitored rainfall with high simulation efficiencies and constrained uncertainty with a second-order (two-pathway) structure. Most of the DOC export in the four headwater basins studied was associated with the faster hydrometric pathway (also modeled in parallel), and was soon exhausted in the slower pathway. A delay in the DOC mobilization became apparent as the ambient temperatures increased. These features of the component pathways were quantified in the dynamic response characteristics (DRCs) identified by RIVC. The model and associated DRCs are intended as a foundation for a better understanding of storm-related DOC dynamics and predictability, given the increasing availability of subhourly DOC concentration data.

The spatiotemporal distribution of dissolved carbon in the main stems and their tributaries along the lower reaches of Heilongjiang River Basin, Northeast China.

PubMed

Wang, Lili; Song, Changchun; Guo, Yuedong

2016-01-01

The Heilongjiang River Basin in the eastern Siberia, one of the largest river basins draining to the North Pacific Ocean, is a border river between China, Mongolia, and Russia. In this study, we examined the spatial and seasonal variability in dissolved organic carbon (DOC), dissolved inorganic carbon (DIC), and dissolved total carbon (DTC) concentrations along lower reaches of Heilongjiang River Basin, China. Water samples were collected monthly along the mouths of main rivers (Heilongjiang River, Wusuli River, and Songhua River) and their ten tributary waters for 2 years. The DOC concentrations of waters ranged from 1.74 to 16.64 mg/L, with a mean value of 8.90 ± 0.27 mg/L (n = 165). Notably, mean DIC concentrations were 9.08 ± 0.31 mg/L, accounting for 13.26∼83.27% of DTC. DIC concentrations increased significantly after the Heilongjiang River passed through Northeast China, while DOC concentrations decreased. Over 50% of DIC concentrations were decreased during exports from groundwater to rice fields and from rice fields to ditches. Water dissolved carbon showed large spatial and temporal variations during the 2-year measurement, suggesting that more frequently samplings were required. Carbon (DIC + DOC) loads from the Heilongjiang River to the Sea of Okhotsk were estimated to be 3.26 Tg C/year in this study, accounting for 0.64% of the global water dissolved carbon flux. DIC export contributed an average of 51.84% of the estimated carbon load in the Heilongjiang River, acting as an important carbon component during riverine transport. Our study could provide some guides on agricultural water management and contribute to more accurately estimate global carbon budgets.

Commonalities in Mercury Behavior in Contrasting Northeastern USA Landscapes

NASA Astrophysics Data System (ADS)

Shanley, J. B.; Scherbatskoy, T.; Schuster, P. F.; Reddy, M. M.; Chalmers, A.

2001-05-01

Generally less than 20% of atmospherically deposited mercury is exported from watersheds in streamflow, but the mercury export that does occur is highly episodic. Our research from diverse landscapes in northern New England, including small forested, agricultural, and urban watersheds as well as some larger rivers discharging to Lake Champlain and the Atlantic Ocean, indicates a consistent positive correlation between Hg concentrations and stream discharge. This relation appears to be driven by increased DOC, POC, and suspended sediment concentrations at increased streamflow. Streamwater Hg analyses pooled from 10 watersheds of diverse size and land use during the 2000 snowmelt within the Sleepers River Research Watershed in northeastern Vermont displayed a high correlation between (1) dissolved Hg and DOC, and (2) particulate Hg and POC. The same correlations held at Nettle Brook, a forested Vermont watershed 100 km west of Sleepers River. At Nettle Brook, DOC and dissolved mercury concentrations were both greater than at Sleepers River but the relation at the two sites was co-linear. In an agricultural watershed in northwestern Vermont, particulate Hg concentrations in streamflow were comparable to those at Nettle Brook despite markedly higher suspended sediment (and presumably POC) concentrations, suggesting the soil Hg pool is depleted by more frequent erosional events. The coupling of organic carbon with mercury may originate in the shallow soil zone; high concentrations of DOC and dissolved Hg were observed in O-horizon soil solution both at Nettle Brook and at some sites in the Adirondack Mountains of New York. Our findings underscore the importance of sampling during high-flow to determine accurate fluxes of Hg in streamflow. It is not clear, however, whether organic carbon actually controls Hg mobility, or whether organic carbon and Hg move in tandem simply as a result of their common source in soil organic matter.

New insights into the source of decadal increase in chemical oxygen demand associated with dissolved organic carbon in Dianchi Lake.

PubMed

Guo, Wei; Yang, Feng; Li, Yanping; Wang, Shengrui

2017-12-15

Dissolved organic carbon (DOC) can be used an alternative index of water quality instead of chemical oxygen demand (COD) to reflect the organic pollution in water. The monitoring data of water quality in a long-term (1990-2013) from Dianchi Lake confirmed the increase trend of COD concentration in the lake since 2007. The similarities and differences in the DOC components between the lake and its sources and the contribution from allochthonous and autochthonous DOC to the total DOC in this lake were determined to elucidate the reason of COD increase based on C/N atomic ratios, stable isotope abundance of carbon and nitrogen, UV-visible spectroscopy, three-dimensional excitation-emission matrix (3DEEM) fluorescence spectroscopy. The terrigenous organic matter showed humic-like fluorescence, and the autochthonous organic matter showed tryptophan-like components. Agricultural runoff (9.5%), leaf litter (7.5%) and urban runoff (13.2%) were the main sources of DOC in the lake. Sewage tail was a major source of organic materials, 3DEEM for the indicates that sewage tail DOC composition did not change markedly over the biodegradation period, indicating that sewage tail contains a high load of DOC that is resistant to further biodegradation and subsequently accumulates in the lake. The change of land use in the catchment and the increase of sewage tail load into the lake are the key factors for the increase in COD concentration in Dianchi Lake. Thus, the lake should be protected by controlling the pollution from the urban nonpoint sources and refractory composition in point sources. Copyright © 2017 Elsevier B.V. All rights reserved.

In-Lake Processes Offset Increased Terrestrial Inputs of Dissolved Organic Carbon and Color to Lakes

PubMed Central

Köhler, Stephan J.; Kothawala, Dolly; Futter, Martyn N.; Liungman, Olof; Tranvik, Lars

2013-01-01

Increased color in surface waters, or browning, can alter lake ecological function, lake thermal stratification and pose difficulties for drinking water treatment. Mechanisms suggested to cause browning include increased dissolved organic carbon (DOC) and iron concentrations, as well as a shift to more colored DOC. While browning of surface waters is widespread and well documented, little is known about why some lakes resist it. Here, we present a comprehensive study of Mälaren, the third largest lake in Sweden. In Mälaren, the vast majority of water and DOC enters a western lake basin, and after approximately 2.8 years, drains from an eastern basin. Despite 40 years of increased terrestrial inputs of colored substances to western lake basins, the eastern basin has resisted browning over this time period. Here we find the half-life of iron was far shorter (0.6 years) than colored organic matter (A420 ; 1.7 years) and DOC as a whole (6.1 years). We found changes in filtered iron concentrations relate strongly to the observed loss of color in the western basins. In addition, we observed a substantial shift from colored DOC of terrestrial origin, to less colored autochthonous sources, with a substantial decrease in aromaticity (-17%) across the lake. We suggest that rapid losses of iron and colored DOC caused the limited browning observed in eastern lake basins. Across a wider dataset of 69 Swedish lakes, we observed greatest browning in acidic lakes with shorter retention times (< 1.5 years). These findings suggest that water residence time, along with iron, pH and colored DOC may be of central importance when modeling and projecting changes in brownification on broader spatial scales. PMID:23976946

Dissolved organic carbon concentration controls benthic primary production: results from in situ chambers in north-temperate lakes

USGS Publications Warehouse

Godwin, Sean C.; Jones, Stuart E.; Weidel, Brian C.; Solomon, Christopher T.

2014-01-01

We evaluated several potential drivers of primary production by benthic algae (periphyton) in north-temperate lakes. We used continuous dissolved oxygen measurements from in situ benthic chambers to quantify primary production by periphyton at multiple depths across 11 lakes encompassing a broad range of dissolved organic carbon (DOC) and total phosphorous (TP) concentrations. Light-use efficiency (primary production per unit incident light) was inversely related to average light availability (% of surface light) in 7 of the 11 study lakes, indicating that benthic algal assemblages exhibit photoadaptation, likely through physiological or compositional changes. DOC alone explained 86% of the variability in log-transformed whole-lake benthic production rates. TP was not an important driver of benthic production via its effects on nutrient and light availability. This result is contrary to studies in other systems, but may be common in relatively pristine north-temperate lakes. Our simple empirical model may allow for the prediction of whole-lake benthic primary production from easily obtained measurements of DOC concentration.

The removal kinetics of dissolved organic matter and the optical clarity of groundwater

USGS Publications Warehouse

Chapelle, Francis H.; Shen, Yuan; Strom, Eric W.; Benner, Ronald

2016-01-01

Concentrations of dissolved organic matter (DOM) and ultraviolet/visible light absorbance decrease systematically as groundwater moves through the unsaturated zones overlying aquifers and along flowpaths within aquifers. These changes occur over distances of tens of meters (m) implying rapid removal kinetics of the chromophoric DOM that imparts color to groundwater. A one-compartment input-output model was used to derive a differential equation describing the removal of DOM from the dissolved phase due to the combined effects of biodegradation and sorption. The general solution to the equation was parameterized using a 2-year record of dissolved organic carbon (DOC) concentration changes in groundwater at a long-term observation well. Estimated rates of DOC loss were rapid and ranged from 0.093 to 0.21 micromoles per liter per day (μM d−1), and rate constants for DOC removal ranged from 0.0021 to 0.011 per day (d−1). Applying these removal rate constants to an advective-dispersion model illustrates substantial depletion of DOC over flow-path distances of 200 m or less and in timeframes of 2 years or less. These results explain the low to moderate DOC concentrations (20–75 μM; 0.26–1 mg L−1) and ultraviolet absorption coefficient values (a254 < 5 m−1) observed in groundwater produced from 59 wells tapping eight different aquifer systems of the United States. The nearly uniform optical clarity of groundwater, therefore, results from similarly rapid DOM-removal kinetics exhibited by geologically and hydrologically dissimilar aquifers.

Representation of Dissolved Organic Carbon in the JULES Dynamic Global Vegetation Model

NASA Astrophysics Data System (ADS)

Nakhavali, Mahdi; Friedlingstein, Pierre; Guenet, Bertrand; Ciais, Philip

2017-04-01

Current global models of the carbon cycle consider only vertical gas exchanges between terrestrial or oceanic reservoirs and the atmosphere, hence not considering lateral transport of carbon from the continent to the oceans. This also means that such models implicitly consider that all the CO2 which is not respired to the atmosphere is stored on land, hence overestimating the land sink of carbon. Moving toward a boundless carbon cycle that is integrating the whole continuum from land to ocean to atmosphere is needed in order to better understand Earth's carbon cycle and to make more reliable projection of its future. Here we present an original representation of Dissolved Organic Carbon (DOC) processes in the Joint UK Land Environment Simulator (JULES). The standard version of JULES represent energy, water and carbon cycles and exchanges with the atmosphere, but only account for water run-off, not including export of carbon from terrestrial ecosystems to the aquatic environments. The aim of the project is to include in JULES a representation of DOC production in terrestrial soils, due to incomplete decomposition of organic matter, its decomposition to the atmosphere, and its export to the river network by leaching. In new developed version of JULES (JULES-DOCM), DOC pools, based on their decomposition rate, are classified into labile and recalcitrant within 3 meters of soil. Based on turnover rate, DOC coming from plant material pools and microbial biomass is directed to labile pool, while DOC from humus is directed to recalcitrant pool. Both of these pools have free (dissolved) and locked (adsorbed) form where just the free pool is subjected to decomposition and leaching. DOC production and decomposition are controlled by rate modifiers (moisture, temperature, vegetation fraction and decomposition rate) at each soil layer. Decomposed DOC is released to the atmosphere following a fixed carbon use efficiency. Leaching accounts for both surface (runoff) and subsurface (groundwater) components and is parameterized as Top soil leaching (from top 20cm) and Bottom soil leaching (down to 3 meters) depending on DOC concentration and runoff leaving that layer. The model parameters are calibrated against specific sites (Brasschaat, Hainich and Carlow) for which observations of DOC concentration and leaching are available. Tuning is performed optimizing parameters such as DOC labile and recalcitrant resident time, DOC vertical distribution and CUE. Once this calibration has been performed at the site level, the model is used for global simulations with the major historical forcing (climate, atmospheric CO2 and land-use changes) in order to estimate the changes of DOC export and their attribution to anthropogenic activities.

The Effects of Permafrost Thaw on Organic Matter Quality and Availability Along a Hill Slope in Northeastern Siberia

NASA Astrophysics Data System (ADS)

Connolly, C. T.; Spawn, S.; Ludwig, S.; Schade, J. D.; Natali, S.

2014-12-01

Climate warming and permafrost thaw in northeastern Siberia are expected to change the quantity and quality of organic matter (OM) transported through watersheds, releasing previously frozen carbon (C) to biologically available pool. Hill slopes have shown to influence the distribution of OM, resulting in a downhill accumulation of available C and nutrients relative to uphill. Here we examine how future permafrost thaw will change OM quality and availability along a hill slope in a larch-dominated watershed. We collected soils from the thawed organic and mineral layers, and 1m deep permafrost cores for dissolved organic C (DOC) and total dissolved N (TDN), C composition from measures of colored dissolved organic matter (CDOM), DOC lability from biodegradable DOC (BDOC) incubations, C and nutrient availability from extracellular-enzyme assays (EEA's), and microbial respiration from aerobic soil incubations. Here we show that organic soils (O), in comparison to mineral soils (M) and permafrost (P) are the most abundant source of C (avg O DOC: 51.6mg/L), exhibiting low molecular complexity (avg O SUVA254: 4.05) and high quality. Evidence suggests permafrost OM may be an equally abundant, and more labile source of C than mineral soils (highest P DOC: 16.1 mg/L, lowest P SUVA254: 6.32; median M DOC: 18.5 mg/L, median M SUVA254: 24.0). Furthermore, we demonstrate that there may be a positive relationship in the rate of C mineralization and distance downhill, showing 15-30% greater CO2 production/gC downhill relative to uphill. Evidence also supports a similar relationship in permafrost DOC content and molecular complexity, showing more DOC of a lower complexity further downhill. This indicates DOC transport may have been occurring through the active layer and downhill during ice-rich permafrost formation, and may supply a labile source of carbon to lowland areas and adjacent stream networks upon thaw.

The effects of particles and dissolved materials on in situ algal pigment fluorescence sensors

NASA Astrophysics Data System (ADS)

Saraceno, J.; Bergamaschi, B. A.; Downing, B. D.

2013-12-01

Field deployable sensors that measure algal pigment fluorescence (APF), such as chlorophyll-a (excitation/emission ca. 470/685 nm), and phycocyanin (ca. 590/685 nm), have been used to estimate algal biomass and study food-web dynamics in coastal and oceanic waters for many years. There is also widespread use of these sensors in real time river-observing networks. However, freshwater systems often possess elevated levels of suspended solids and dissolved organic material that can interfere with optical measurements. Data collected under conditions that result in interferences may not be comparable across time and between sites unless the data are appropriately corrected. Using standard reference materials and a surrogate for algal fluorescence (Rhodamine WT), lab experiments were conducted on several commercially available sensors to quantify sensitivity to interferences over a range of naturally occurring surface water conditions (DOC : 0-30 mg/L and turbidity: 0- 1000 FNU ). Chlorophyll-a sensors exhibited a slight but significant positive bias (<1%) at DOC concentrations < 2 mg/L, and a negative, non-linear bias at DOC concentrations >2 mg/L, with signal quenching reaching a maximum of 15% at 30 mg/L DOC. All phycocyanin sensors displayed a positive non-linear bias with DOC concentration, reaching a maximum of 40% difference at 30 mg/L DOC. Both chlorophyll-a and phycocyanin sensors showed a positive linear relationship with suspended solids concentration (as indicated by turbidity).The effect of suspended solids on APF output can be explained by the detection of scattered excitation light (leaking through emission filters). Similar qualitative effects were observed for the sensors tested, though the magnitude of the effect varied among sensor type. This indicates that differences in sensor designs such as geometry, wavelength and signal post processing techniques is related to its sensitivity to interferences. Although sensors exhibited significant cross sensitivity to interferences, our results indicate that simple corrections can largely remove sensor bias. To remove bias due to optical interferences and generate high quality, repeatable APF data, knowledge of the optical properties of the matrix and/or coincident measures of the concentration of suspended solids and dissolved organics (through surrogates such as turbidity and colored dissolved organic matter (cDOM) fluorescence, respectively), are typically needed.

Physical and biogeochemical controls on polymictic behavior in Sierra Nevada stream pools

NASA Astrophysics Data System (ADS)

Lucas, R. G.; Conklin, M. H.; Tyler, S. W.; Suarez, F. I.; Moran, J. E.; Esser, B. K.

2011-12-01

We observed polymictic behavior in stream pools in a low gradient montane meadow in the southern Sierra Nevada mountains, California. Thermal stratification in stream pools has been observed in various environments; stratification generally persists where the buoyancy forces created by a variation in water density, as a function of water temperature, are able to overcome turbulent forces resulting from stream flow. Because the density gradient creates a relatively weak buoyancy force, low flow conditions are generally required in order to overcome the turbulent forces. In some studies, a cold water source in to the pool bottoms can help to increase the density gradient and perpetuate thermal stratification. Our study took place in Long Meadow, Sequoia National Park, California. Long Meadow lies in the Wolverton Creek watershed and is part of the Southern Sierra Critical Zone Observatory. The 1-4 m diameter and 1-2 m deep pools in our study stratified thermally during the day and mixed completely at night. The low gradient of the meadow provided low stream flows. Piezometers in the meadow indicated groundwater discharge into the meadow in the months during which stratification was observed. Radon 222 activity measured in the pools also indicated groundwater influx to the pool bottoms. We used Fluent, a computational fluid dynamics equation solver, to construct a model of one of the observed pools. Initially we attempted to model the physical mechanisms controlling thermal stratification in the pool including stream flow, groundwater discharge, solar radiation, wind speed, and air, stream and ground water temperatures. Ultimately we found the model best agreed with our observed pool temperatures when we considered the light attenuation coefficients as a function of the dissolve organic carbon (DOC) concentration. Elevated DOC concentrations are expected in low stream flow regimes associated with highly organic soils such as a montane meadow. DOC concentrations measured in samples collected from the meadow stream, pools, and ground water wells ranged from 3.09 to 5.25 mg/L. We used a power equation taken from the literature to vary the visible light attenuation with DOC values measured in the meadow system. Light attenuation coefficients determined from measured DOC concentrations ranged from 0.507 m-1 to 0.899 m-1. The results from our modeling efforts indicate that in low flow streams and rivers elevated concentrations of DOC can increase the potential for thermal stratification in stream pools.

Dissolved Organic Carbon: Nitrate Ratios as a Driver of Methane Fluxes in Stream Ecosystems

NASA Astrophysics Data System (ADS)

Sullivan, B. W.; Wymore, A.; Schade, J. D.; McDowell, W. H.

2016-12-01

Fluvial ecosystems are poorly understood components of the global methane (CH4) budget because the ecology of CH4 fluxes in streams has yet to be sufficiently elucidated. Both CH4 production and uptake via oxidation are microbially mediated processes, but it is unclear where in the fluvial environment are the sources and sinks of CH4 and what role terrestrial inputs of carbon (C) and nutrients have on the magnitude and direction of CH4 flux. To address these uncertainties, we measured CH4 fluxes in a laboratory incubation from two temperate headwater streams that differed in ambient dissolved organic carbon (DOC) and nitrate (NO3-) concentrations. We amended stream water and sediment microcosms from each site with labile DOC from senesced leaf litter to assess how DOC concentration and the DOC:NO3- ratio affect proximate controls on CH4 flux. Lastly, we manipulated sediment and water column ratios (0-100%) to estimate sources and fates of CH4 flux within the ecosystem. We measured CH4 fluxes for the first 120 minutes of the incubation to simulate short-term, in stream processes. Initially, streams were a source of methane, but switched to a sink within 120 minutes. Methane fluxes were statistically similar in both stream sediment and water, suggesting that microbial processing of CH4 has similar directionality and magnitude in each environment. Both CH4 oxidation and production were significantly correlated with the DOC: NO3- ratio over the course of the incubation. Early in the incubation, increasing DOC: NO3- increased CH4 flux, but late in the incubation, increasing DOC: NO3- increased CH4 oxidation. Together, our results challenge existing paradigms of CH4 flux in the fluvial environment and identify the DOC:NO3- ratio as a possible mechanism that can explain spatial and temporal CH4 flux patterns in streams.

Antecedent conditions control carbon loss and downstream water quality from shallow, damaged peatlands.

PubMed

Grand-Clement, E; Luscombe, D J; Anderson, K; Gatis, N; Benaud, P; Brazier, R E

2014-09-15

Losses of dissolved organic carbon (DOC) from drained peatlands are of concern, due to the effects this has on the delivery of ecosystem services, and especially on the long-term store of carbon and the provision of drinking water. Most studies have looked at the effect of drainage in deep peat; comparatively, little is known about the behaviour of shallow, climatically marginal peatlands. This study examines water quality (DOC, Abs(400), pH, E4/E6 and C/C) during rainfall events from such environments in the south west UK, in order to both quantify DOC losses, and understand their potential for restoration. Water samples were taken over a 19 month period from a range of drains within two different experimental catchments in Exmoor National Park; data were analysed on an event basis. DOC concentrations ranging between 4 and 21 mg L(-1) are substantially lower than measurements in deep peat, but remain problematic for the water treatment process. Dryness plays a critical role in controlling DOC concentrations and water quality, as observed through spatial and seasonal differences. Long-term changes in depth to water table (30 days before the event) are likely to impact on DOC production, whereas discharge becomes the main control over DOC transport at the time scale of the rainfall/runoff event. The role of temperature during events is attributed to an increase in the diffusion of DOC, and therefore its transport. Humification ratios (E4/E6) consistently below 5 indicate a predominance of complex humic acids, but increased decomposition during warmer summer months leads to a comparatively higher losses of fulvic acids. This work represents a significant contribution to the scientific understanding of the behaviour and functioning of shallow damaged peatlands in climatically marginal locations. The findings also provide a sound baseline knowledge to support research into the effects of landscape restoration in the future. Crown Copyright © 2014. Published by Elsevier B.V. All rights reserved.

Seasonal variation in the nature of DOM in a river and drinking water reservoir of a closed catchment.

PubMed

Awad, John; van Leeuwen, John; Chow, Christopher W K; Smernik, Ronald J; Anderson, Sharolyn J; Cox, Jim W

2017-01-01

Dissolved organic matter (DOM) in surface waters used for drinking purposes can vary markedly in character depending on its source within catchments and the timing and intensity of rainfall events. Here we report the findings of a study on the character and concentration of DOM in waters collected during different seasons from Myponga River and Reservoir, South Australia. The character of DOM was assessed in terms of its treatability by enhanced coagulation and potential for disinfection by-product i.e. trihalomethane (THM) formation. During the wet seasons (winter and spring), water samples from the river had higher DOC concentrations (X¯: 21 mg/L) and DOM of higher average molecular weight (AMW: 1526 Da) than waters collected during the dry seasons (summer and autumn: DOC: 13 mg/L; AMW: 1385 Da). Even though these features led to an increase in the percentage removal of organics by coagulation with alum (64% for wet compared with 53% for dry season samples) and a lower alum dose rate (10 versus 15 mg alum/mg DOC removal), there was a higher THM formation potential (THMFP) from wet season waters (treated waters: 217 μg/L vs 172 μg/L). For reservoir waters, samples collected during the wet seasons had an average DOC concentration (X¯: 15 mg/L), percentage removal of organics by alum (54%), alum dose rates (13 mg/mg DOC) and THMFP (treated waters: 207 μg/L) that were similar to samples collected during the dry seasons (mean DOC: 15 mg/L; removal of organics: 52%; alum dose rate: 13 mg/mg DOC; THMFP: 212 μg/L for treated waters). These results show that DOM present in river waters and treatability by alum are highly impacted by seasonal environmental variations. However these in reservoir waters exhibit less seasonal variability. Storage of large volumes of water in the reservoir enables mixing of influent waters and stabilization of water quality. Crown Copyright © 2016. Published by Elsevier Ltd. All rights reserved.

Data-based mechanistic modeling of dissolved organic carbon load through storms using continuous 15-minute resolution observations within UK upland watersheds

NASA Astrophysics Data System (ADS)

Jones, T.; Chappell, N. A.

2013-12-01

Few watershed modeling studies have addressed DOC dynamics through storm hydrographs (notable exceptions include Boyer et al., 1997 Hydrol Process; Jutras et al., 2011 Ecol Model; Xu et al., 2012 Water Resour Res). In part this has been a consequence of an incomplete understanding of the biogeochemical processes leading to DOC export to streams (Neff & Asner, 2001, Ecosystems) & an insufficient frequency of DOC monitoring to capture sometimes complex time-varying relationships between DOC & storm hydrographs (Kirchner et al., 2004, Hydrol Process). We present the results of a new & ongoing UK study that integrates two components - 1/ New observations of DOC concentrations (& derived load) continuously monitored at 15 minute intervals through multiple seasons for replicated watersheds; & 2/ A dynamic modeling technique that is able to quantify storage-decay effects, plus hysteretic, nonlinear, lagged & non-stationary relationships between DOC & controlling variables (including rainfall, streamflow, temperature & specific biogeochemical variables e.g., pH, nitrate). DOC concentration is being monitored continuously using the latest generation of UV spectrophotometers (i.e. S::CAN spectro::lysers) with in situ calibrations to laboratory analyzed DOC. The controlling variables are recorded simultaneously at the same stream stations. The watersheds selected for study are among the most intensively studied basins in the UK uplands, namely the Plynlimon & Llyn Brianne experimental basins. All contain areas of organic soils, with three having improved grasslands & three conifer afforested. The dynamic response characteristics (DRCs) that describe detailed DOC behaviour through sequences of storms are simulated using the latest identification routines for continuous time transfer function (CT-TF) models within the Matlab-based CAPTAIN toolbox (some incorporating nonlinear components). To our knowledge this is the first application of CT-TFs to modelling DOC processes. Furthermore this allows a data-based mechanistic (DBM) modelling philosophy to be followed where no assumptions about processes are defined a priori (given that dominant processes are often not known before analysis) & where the information contained in the time-series is used to identify multiple structures of models that are statistically robust. Within the final stage of DBM, biogeochemical & hydrological processes are interpreted from those models that are observable from the available stream time-series. We show that this approach can simulate the key features of DOC dynamics within & between storms & that some of the resultant response characteristics change with varying DOC processes in different seasons. Through the use of MISO (multiple-input single-output) models we demonstrate the relative importance of different variables (e.g., rainfall, temperature) in controlling DOC responses. The contrasting behaviour of the six experimental catchments is also reflected in differing response characteristics. These characteristics are shown to contribute to understanding of basin-integrated DOC export processes & to the ecosystem service impacts of DOC & color on commercial water treatment within the surrounding water supply basins.

Sources, bioavailability, and photoreactivity of dissolved organic carbon in the Sacramento-San Joaquin River Delta

USGS Publications Warehouse

Stepanauskas, R.; Moran, M.A.; Bergamaschi, B.A.; Hollibaugh, J.T.

2005-01-01

We analyzed bioavailability, photoreactivity, fluorescence, and isotopic composition of dissolved organic carbon (DOC) collected at 13 stations in the Sacramento-San Joaquin River Delta during various seasons to estimate the persistence of DOC from diverse shallow water habitat sources. Prospective large-scale wetland restorations in the Delta may change the amount of DOC available to the food web as well as change the quality of Delta water exported for municipal use. Our study indicates that DOC contributed by Delta sources is relatively refractory and likely mostly the dissolved remnants of vascular plant material from degrading soils and tidal marshes rather than phytoplankton production. Therefore, the prospective conversion of agricultural land into submerged, phytoplankton-dominated habitats may reduce the undesired export of DOC from the Delta to municipal users. A median of 10% of Delta DOC was rapidly utilizable by bacterioplankton. A moderate dose of simulated solar radiation (286 W m-2 for 4 h) decreased the DOC bioavailability by an average of 40%, with a larger relative decrease in samples with higher initial DOC bioavailability. Potentially, a DOC-based microbial food web could support ???0.6 ?? 109 g C of protist production in the Delta annually, compared to ???17 ?? 109 g C phytoplankton primary production. Thus, DOC utilization via the microbial food web is unlikely to play an important role in the nutrition of Delta zooplankton and fish, and the possible decrease in DOC concentration due to wetland restoration is unlikely to have a direct effect on Delta fish productivity. ?? Springer 2005.

Effects of Volcanic Pumice Inputs on Microbial Community Composition and Dissolved C/P Ratios in Lake Waters: an Experimental Approach.

PubMed

Modenutti, B E; Balseiro, E G; Bastidas Navarro, M A; Lee, Z M; Souza, M S; Corman, J R; Elser, J J

2016-01-01

Volcanic eruptions discharge massive amounts of ash and pumice that decrease light penetration in lakes and lead to concomitant increases in phosphorus (P) concentrations and shifts in soluble C/P ratios. The consequences of these sudden changes for bacteria community composition, metabolism, and enzymatic activity remain unclear, especially for the dynamic period immediately after pumice deposition. Thus, the main aim of our study was to determine how ambient bacterial communities respond to pumice inputs in lakes that differ in dissolved organic carbon (DOC) and P concentrations and to what extent these responses are moderated by substrate C/P stoichiometry. We performed an outdoor experiment with natural lake water from two lakes that differed in dissolved organic carbon (DOC) concentration. We measured nutrient concentrations, alkaline phosphatase activity (APA), and DOC consumption rates and assessed different components of bacterial community structure using next-generation sequencing of the 16S rRNA gene. Pumice inputs caused a decrease in the C/P ratio of dissolved resources, a decrease in APA, and an increase in DOC consumption, indicating reduced P limitation. These changes in bacteria metabolism were coupled with modifications in the assemblage composition and an increase in diversity, with increases in bacterial taxa associated with biofilm and sediments, in predatory bacteria, and in bacteria with gliding motility. Our results confirm that volcanic eruptions have the potential to alter nutrient partitioning and light penetration in receiving waterways which can have dramatic impacts on microbial community dynamics.

Controls on stream water dissolved mercury in three mid-Appalachian forested headwater catchments

NASA Astrophysics Data System (ADS)

Riscassi, Ami L.; Scanlon, Todd M.

2011-12-01

Determining the controls on dissolved mercury (HgD) transport is necessary to improve estimations of export from unmonitored watersheds and to forecast responses to changes in deposition and other environmental forcings. Stream water HgD and dissolved organic carbon (DOC) were evaluated over a range of discharge conditions in three streams within Shenandoah National Park, VA. Watersheds are distinguished by stream water pH (ranging from neutral to acidic) and soil size fractioning (ranging from clays to sands). At all sites, discharge was a significant but poor predictor of HgD concentrations (r2 from 0.13-0.52). HgD was strongly coupled with DOC at all sites (r2 from 0.74-0.89). UV absorbance at 254 nm (UV254), a proxy for DOC quantity and quality, slightly improved the predictions of HgD. Mean DOC quality differed between streams, with less aromatic DOC mobilized from the more acidic watershed. The site with less aromatic DOC and sandy soils mobilized more Hg to the stream for the same quantity and quality of DOC, likely due to the reduced capacity of the larger-grained soils to retain Hg, leaving a greater fraction associated with the organic matter. A similar amount of 0.54 ng HgD/mg DOC is transported at all sites, suggesting the less aromatic DOC transports less Hg per unit DOC, offsetting the effects of soil type. This research demonstrates that soil composition and DOC quality influence HgDexport. We also provide evidence that soil organic carbon is a primary control on Hg-DOC ratios (0.12-1.4 ng mg-1) observed across the U.S. and Sweden.

Treatment of melanoidin wastewater by anaerobic digestion and coagulation.

PubMed

Arimi, Milton M; Zhang, Yongjun; Götz, Gesine; Geißen, Sven-Uwe

2015-01-01

Melanoidins are dark-coloured recalcitrant pollutants found in many industrial wastewaters including coffee-manufacturing effluent, molasses distillery wastewater (MDWW) and other wastewater with molasses as the raw material. The wastewaters are mostly treated with anaerobic digestion after some dilution to minimize the inhibition effect. However, the dark colour and recalcitrant dissolved organic carbon (DOC) mainly caused by melanoidin are not effectively removed. The aim of this study was to investigate the removal of colour and remnant DOC by different coagulants from anaerobically digested MDWW. From the six coagulants tested, ferric chloride had the highest melanoidin (48%), colour (92.7%) and DOC (63.3%) removal at pH 5 and a dosage of 1.6 g/l. Both polymer and inorganic salt coagulants tested had optimal colour, melanoidin and DOC removal at acidic pH. The molecular size distribution of synthetic melanoidins by liquid chromatography-organic carbon detection indicated a preferential removal of high-molecular-weight melanoidins over low weight melanoidins by the coagulation. Further studies should focus on how to improve biodegradability of the treated effluent for it to be reused as dilution water for anaerobic digestion.

Mangroves, a major source of dissolved organic carbon to the oceans

NASA Astrophysics Data System (ADS)

Dittmar, Thorsten; Hertkorn, Norbert; Kattner, Gerhard; Lara, RubéN. J.

2006-03-01

Organic matter, which is dissolved in low concentrations in the vast waters of the oceans, contains a total amount of carbon similar to atmospheric carbon dioxide. To understand global biogeochemical cycles, it is crucial to quantify the sources of marine dissolved organic carbon (DOC). We investigated the impact of mangroves, the dominant intertidal vegetation of the tropics, on marine DOC inventories. Stable carbon isotopes and proton nuclear magnetic resonance spectroscopy showed that mangroves are the main source of terrigenous DOC in the open ocean off northern Brazil. Sunlight efficiently destroyed aromatic molecules during transport offshore, removing about one third of mangrove-derived DOC. The remainder was refractory and may thus be distributed over the oceans. On a global scale, we estimate that mangroves account for >10% of the terrestrially derived, refractory DOC transported to the ocean, while they cover only <0.1% of the continents' surface.

[Spatial distribution of COD and the correlations with other parameters in the northern region of Lake Taihu].

PubMed

Zhang, Yun-lin; Yang, Long-yuan; Qin, Bo-qiang; Gao, Guang; Luo, Lian-cong; Zhu, Guang-wei; Liu, Ming-liang

2008-06-01

Spatial variation of chemical oxygen demand (COD) concentration was documented and significant correlations between COD concentration and chromophoric dissolved organic matter (CDOM) absorption, fluorescence, DOC concentration were found based on a cruise sampling in the northern region of Lake Taihu in summer including 42 samplings. The possible source of COD was also discussed using every two cruise samplings in summer and winter, respectively. The COD concentration ranged from 3.77 to 7.96 mg x L(-1) with a mean value of (5.90 +/- 1.54) mg x L(-1). The mean COD concentrations in Meiliang Bay and the central lake basin were (6.93 +/- 0.89) mg x L(-1) and (4.21 +/- 0.49) mg x L(-1) respectively. A significant spatial difference was found between Meiliang Bay and the central lake basin in COD concentration, CDOM absorption coefficient, fluorescence, DOC and phytoplankton pigment concentrations, decreasing from the river mouth to inner bay, outer bay and the central lake basin. Significant correlations between COD concentration and CDOM absorption, fluorescence, DOC concentration, suggested that COD concentration could be estimated and organic pollution could be assessed using CDOM absorption retrieved from remote sensing images. Significant and positive correlation was found between COD concentration and chlorophyll a concentration in summer. However, the correlation was weak or no correlation was found in winter. Furthermore, a significant higher COD concentration was found in summer than in winter (p < 0.001). Our results indicated that degradation of phytoplankton blooms was the main source of COD in summer, except for river terrestrial input.

Occurrence and Distribution of Mercury in the SurficialAquifer, Long Neck Peninsula, Sussex County, Delaware, 2003-04

USGS Publications Warehouse

Koterba, Michael T.; Andres, A. Scott; Vrabel, Joseph; Crilley, Dianna M.; Szabo, Zoltan; DeWild, John F.; Aiken, George R.; Reyes-Padro, Betzaida

2006-01-01

In January 2001, mercury (Hg) was detected (500 nanograms per liter, ng/L, or greater) in the distribution system of the Long Neck Water Company (LNWC), Pot Nets, Delaware. By April 2001, two LNWC production wells had been taken off-line because discharge concentrations of total mercury (HgT) either had exceeded or approached the Federal limit of 2,000 ng/L. From October 2003 through January 2005, the U.S. Geological Survey, Delaware Geological Survey, and Delaware Department of Natural Resources and Environmental Control conducted a cooperative study to (a) determine if the Hg contamination was widespread, (b) identify possible forms of Hg in ground water, and (c) examine Hg occurrence in relation to (geo)chemical conditions and characteristics of ground water and sediment in the surficial aquifer on the Long Neck Peninsula, Sussex County, Delaware. An initial water-quality survey conducted with samples from 22 production wells revealed that concentrations of HgT in ground water in the surficial aquifer ranged from 0.11 to 1,820 ng/L. Shallow ground water (less than 120 feet below land surface) throughout most of the peninsula, including that which contained elevated concentrations of HgT (exceeding 100 ng/L), appeared to be affected by human activities. All samples contained volatile organic compounds (VOCs) and elevated nitrate-nitrogen (NO3-N, exceeding 0.4 milligrams per liter, mg/L). Most (16 of 22) samples had elevated specific conductance (SC, in excess of 100 microsiemens per centimeter at 25 degrees Celsius). Elevated concentrations of HgT, however, only occurred in five production wells in the Pot Nets Bayside and Lakeside communities. The vertical distribution of HgT in shallow ground water (less than 80 feet below land surface) was determined with samples collected at 5 to 6 vertical-nest short-screened (2 - 5-foot length) monitoring wells installed near Bayside and Lakeside production wells with the highest HgT concentrations (exceeding 1,000 ng/L). Elevated concentrations ofHgT (100-6,380 ng/L) occurred in the shallow aquifer near each well at different depths. Chemical analyses of selected soil, fill, and aquifer sediment samples, obtained during the installation of nested wells, indicated that little HgT occurred in soil or fill at either site (40 micrograms per kilogram, ?g/kg, or less). No HgT was detected (less than 20 ?g/kg) in aquifer sediment samples. These low HgT concentrations imply that neither the soil, fill, nor aquifer sediment was a likely source of the elevated Hg in ground water. Given Hg occurrence appeared to be a ground-water transport phenomenon, the forms of Hg in transport were investigated. Differences in HgT concentrations between raw and filtered (0.1- and (or) 0.4-absolute micrometer pore size) samples from nested wells were random in sign and similar in magnitude to the variability in measuring HgT attributed to field and laboratory methods (? 5-10 percent, for HgT concentrations exceeding 100 ng/L). Thus, Hg transport likely occurred in a dissolved or fine-colloidal nonparticulate phase. Methyl mercury (HgMe) only was detected at low concentrations (0.06 ng/L or less) in nested-well samples with low to moderate concentrations of HgT (less than 366 ng/L). Whether HgMe occurred at similar concentrations in samples with high HgT concentrations was unresolved due to a sample-matrix interference problem. Potential complex forms of Hg were investigated in relation to the occurrence of selected ligands (organic carbon, sulfide, and chloride concentrations) and geochemical conditions (for example, pH and dissolved oxygen concentrations). Only dissolved organic carbon (DOC) appeared directly related to Hg occurrence. Elevated concentrations of HgT and DOC co-occurred in ground water at both Pot Nets sites. The average concentration of DOC was about four times greater in samples from the Pot Nets wells with the highest HgT concentrations (exceeding 1,000 ng/L) than in most Pot Nets o

Effect of inorganic N enrichment on basal pelagic production in boreal unproductive lakes along a gradient of DOC concentration - results after 1 year of fertilization

NASA Astrophysics Data System (ADS)

Deininger, Anne; Bergström, Ann-Kristin

2013-04-01

Input of inorganic nitrogen (N) in boreal unproductive lakes is steadily increasing due to anthropogenic deposition and usage of artificial fertilizers. N enrichment is predicted to have a major impact on the ecosystem productivity and food web structure in unproductive clear-water and humic lakes. For a long time, pelagic primary production (PP) has been mainly regarded as being phosphorus (P) limited. However, recent studies have shown that this is not true for unproductive lakes in northern Sweden, where phytoplankton is mainly N limited. Addition of inorganic N should therefore increase phytoplankton growth in these lake ecosystems. Bacterial production (BP) in the pelagic habitat, on the other hand, is usually limited by P. Nevertheless, elevated N could have a stimulating effect on BP through enhanced leakage of dissolved organic carbon (DOC) from phytoplankton following enhanced N availability and higher PP. Further, unproductive lakes vary naturally in their DOC content which affects overall nutrient- (N and P), energy- and carbon availability (light, C) for the basal producers (phytoplankton, bacteria). It is still not clear how higher inorganic N availability affects primary- and bacterial production in the pelagic in lakes with varying DOC content. We subsequently assessed this question by conducting whole-lake fertilization experiments with inorganic N additions in 6 lakes with varying DOC concentrations (2 low DOC; 2 medium DOC; 2 high DOC). For each DOC level one lake functioned as a reference and one was fertilized with N. Year 2011 was a reference year (all lakes) and 2012 was the first year of fertilization (i.e. in 3 lakes). Measurements included basal productivity such as primary production and bacteria production, lake water chemistry and physical parameters (i.e. light, temperature). The results of this study will help to develop a conceptual understanding of how increased inorganic N availability (through land use such as forestry and/or enhanced N deposition) affects basal productivity in boreal lakes which can have consequences for overall whole lake-ecosystem productivity and functioning.

Riverine organic matter composition and fluxes to Hudson Bay

NASA Astrophysics Data System (ADS)

Kuzyk, Z. Z. A.; Macdonald, R. W.; Goni, M. A.; Godin, P.; Stern, G. A.

2016-12-01

With warming in northern regions, many changes including permafrost degradation, vegetation alteration, and wildfire incidence will impact the carbon cycle. Organic carbon (OC) carried by river runoff to northern oceans has the potential to provide integrated evidence of these impacts. Here, concentrations of dissolved (DOC) and particulate (POC) OC are used to estimate terrestrial OC transport in 17 major rivers draining varied vegetative and permafrost conditions into Hudson Bay and compositional data (lignin and 14C) to infer OC sources. Hudson Bay lies just south of the Arctic Circle in Canada and is surrounded by a large drainage basin (3.9 × 106 km2) dominated by permafrost. Analysis of POC and DOC in the 17 rivers indicates that DOC dominates the total OC load. The southern rivers dominate. The Nelson and Churchill Rivers to the southwest are particularly important suppliers of OC partly because of large drainage basins but also perhaps because of impacts by hydroelectric development, as suggested by a 14C age of DOC in the Churchill River of 2800 years. Higher DOC and POC concentrations in the southern rivers, which have substantive areas only partially covered by permafrost, compared to northern rivers draining areas with complete permafrost cover, implies that warming - and hence permafrost thawing - will lead to progressively higher DOC and POC loads for these rivers. Lignin composition in the organic matter (S/V and C/V ratios) reveals mixed sources of OC consistent with the dominant vegetation in the river basins. This vegetation is organized by latitude with southern regions below the tree line enriched by woody gymnosperm sources (boreal forest) and northern regions enriched with organic matter from non-woody angiosperms (flowering shrubs, tundra). Acid/Aldehyde composition together with Δ14C data for selected DOC samples suggest that most of the lignin has undergone oxidative degradation, particularly the DOC component. However, high Δ14C ages did not co-occur with high [Ad/Al] ratios, suggesting that riverine DOC preserved (frozen) for extensive periods is now being released. Although permafrost thaw within the Hudson Bay drainage has already commenced, this meridional river study provides a benchmark against which to evaluate future change.

Oxygen consumption and labile dissolved organic carbon uptake by benthic biofilms

NASA Astrophysics Data System (ADS)

de Falco, Natalie; Boano, Fulvio; Arnon, Shai

2015-04-01

Biogeochemical activity in streams is often magnified at interfaces, such as in the case of biofilm growth near the surface of the stream sediments. The objective of this study was to evaluate the relative importance of surficial biofilms versus the biofilm in the hyporheic zone to the processes of biodegradation of a labile dissolved organic carbon (DOC) and to oxygen consumption. Experiments were conducted in a recirculating flume, equipped with a drainage system that enables the control on losing and gaining fluxes. A surficial biofilm was developed over a sandy streambed with dune-shaped bed forms, by providing labile DOC (sodium benzoate) and nitrate. Homogeneously distributed biofilm was obtained by the same feeding strategy but with mixing the sediments manually on a daily basis. After the biofilm growth period, transformation of the labile DOC under different overlying velocities and losing or gaining fluxes was studied after spiking with sodium benzoate and by monitoring the decrease in DOC concentration in the bulk water over time using an online UV/Vis spectrophotometer. In addition, oxygen profiles across the water-streambed interface were measured at different locations along the bed form using oxygen microelectrodes. Preliminary results showed that the rate of labile DOC degradation increased exponentially with increasing overlying water velocity, regardless of the type of biofilm. Gaining and losing conditions did not play a critical role in the DOC degradation regardless of the type of biofilm, because the labile DOC was quickly utilized close to the surface. Under losing conditions, complete depletion of oxygen was observed within the top 5 millimeters, regardless of the biofilm type. In contrast, oxygen profiles under gaining condition showed an incomplete consumption of oxygen followed by an increase in the concentration of oxygen deeper in the sediments due to the upward flow of oxygenated groundwater. The results suggest that the transformation of labile DOC occurs in the upper millimeters of the streambed, and the size and shape of the hyporheic flow paths are less important for aerobic activity. In addition, the effect of overlying water velocity on labile DOC transformation was shown to be more influential than losing and gaining fluxes.

Organic carbon fluxes in stemflow, throughfall and rainfall in an olive orchard

NASA Astrophysics Data System (ADS)

Lombardo, L.; Vanwalleghem, T.; Gomez, J. A.

2012-04-01

The importance of rainfall distribution under the vegetation canopy for nutrient cycling of forest ecosystems has been widely studied (e.g. Kolkai et al., 1999, Bath et al., 2011). It has been demonstrated how throughfall and stemflow reach the soil as chemically-enriched water, by incorporating soluble organic and inorganic particles deriving from plant exudates and from atmospheric depositions (dryfall and wetfall) present on the surfaces of the plant (leaves, bark, fruits). Dissolved (DOC) and particulate (POC) organic carbon inputs from stem- and canopy-derived hydrologic fluxes are small but important components of the natural carbon cycle. DOC has also the capability to form complexes that control the transport and solubility of heavy metals in surface and ground waters, being composed for the most part (75-90%) of fulvic, humic or tanninic compounds, and for the resting part of molecules like carbohydrates, hydrocarbons, waxes, fatty acids, amino and hydroxy acids. However, very little data is available for agricultural tree crops, especially olive trees. In this sense, the objective of this work is to investigate the concentration and fluxes of organic carbon in rainfall, throughfall, and stemflow in a mature olive orchard located in Cordoba, in Southern Spain and to relate them to rainfall characteristics and tree physiology. The measurements started in October 2011. Four high density polyethylene bottles with 18-cm-diameter polyethylene funnels for throughfall collection were placed beneath the canopy of each of the three selected olive trees; four more collectors were placed in open spaces in the same orchard for rainfall sampling. Stemflow was collected through PVC spiral tubes wrapped around the trunks and leading into collection bins. The throughflow sampling points were chosen randomly. Total and dissolved organic carbon concentrations in unfiltered (TOC) and filtered (0.45 µm membrane filter, DOC) collected waters were measured using a TOC analyzer with a high temperature combustion system and infrared detection of the evolved CO2. The difference in concentration between TOC and DOC defined the POC concentration. Leaf area density (LAD) and leaf area index (LAI) of olive trees were calculated using the LAI-2000 plant canopy analyzer (PCA) (Li-Cor). Stemflow and throughfall resulted both influenced by the characteristics of precipitations (amount, time of the year), canopy volume and leaf characteristics, with stemflow showing, in average, higher DOC and POC concentration values compare to throughfall. Throughfall resulted between 4 and 17 times more concentrated DOC than rainfall, but highlighted a high site-specific variability related to the canopy architecture.

Is the blocking of drainage channels in upland peats an effective means of reducing DOC loss at the catchment scale?

NASA Astrophysics Data System (ADS)

Turner, Kate; Worrall, Fred

2010-05-01

Only 3% of the earths land surface is covered by peatland yet boreal and subarctic peatlands store approximately 15-30% of the World's soil carbon as peat (Limpens et al. 2008). In comparison British bogs store carbon equivalent to 20 years worth of national emissions. The loss of carbon from these areas in the form of dissolved organic carbon (DOC) is increasing and it is expected to have grown by up to 40% by 2018. Extensive drainage of UK peatlands has been associated with dehydration of the peat, an increase in water colour and a loss of carbon storage. It has been considered that the blocking of these drainage channels represents a means of peat restoration and a way of reducing DOC loss. This study aims to assess the effectiveness of this drain blocking at both an individual drain scale and at a larger catchment scale. Gibson et al. (2009) considered the effects of blocking at a solely individual drain scale finding that a 20% drop in DOC export was recorded post blocking however this decrease was due to a reduction in water yield rather than a reduction in DOC concentration with the concentration record showing no significant reduction. The effect of external parameters become more pronounced as the DOC record is examined at larger scales. The catchment is an open system and water chemistry will be influence by mixing with water from other sources. Also it is likely that at some point the drains will cut across slope leading to the flow of any highly coloured water down slope, bypassing the blockages, and entering the surface waters downstream. Degradation of DOC will occur naturally downstream due to the effects of light and microbial activity. There is, consequently, a need to examine the wider effects of drain blocking at a catchment scale to ensure that what is observed for one drain transfers to the whole catchment. A series of blocked and unblocked catchments were studied in Upper Teesdale, Northern England. Drain water samples were taken at least daily at nine localities. These sites were located such that individual drains could be monitored in the context of a larger catchment. Water table depth, flow and weather parameters were recorded along with the collection of runoff and soil water samples. A detailed sampling programme was undertaken in which a series of drains were studied in the 12 months prior to and post blocking. This approach has allowed the effects of blocking on the carbon budget, water balance and flow pathways to be considered. Results indicate that the blocking of zero order drainage channels leads to a decrease in DOC export on an individual drain scale. However, this is due to a reduction in water yield rather than concentration. Concentrations are seen to rise by a small yet statistically significant amount in blocked zero order streams. The effect at a larger scale is more complex. Annual export values in the unblocked control catchment show a rise from zero to first order streams indicating that water is being added to the system at this scale from external spatially variable sources. This pattern is also recognised in the blocked catchment. The DOC concentration record in blocked drains at this larger scale however indicated a reduction relative to the unblocked catchment. This reduction points to a change in flow pathways post blocking as highly coloured water re-navigates its way downstream. References: Gibson H, Worrall F, Burt TP, Adamson JK (2009) DOC budgets of drained peat catchments: implications for DOC production in peat soils, Hydrological Processes 23(13) 1901-1911 Limpens J (2008) Peatlands and the carbon cycle: from local processes to global implications- a synthesis, Biogeosciences 5 1475-1491

The Age of Terrestrial Carbon Export and Rainfall Intensity in a Temperate River Headwater System

NASA Astrophysics Data System (ADS)

Tittel, J.; Büttner, O.; Freier, K.; Heiser, A.; Sudbrack, R.; Ollesch, G.

2013-12-01

Riverine dissolved organic carbon (DOC) supports the production of estuaries and coastal ecosystems, constituting one of the most actively recycled pools of the global carbon cycle. A substantial proportion of DOC entering oceans is highly aged, but its origins remain unclear. Significant fluxes of old DOC have never been observed in temperate headwaters where terrestrial imports take place. Here, we studied the radiocarbon age of DOC in three streams draining forested headwater catchments of the river Mulde (Ore Mountains, Germany). We found modern DOC at moderately dry and moderately wet conditions as well as at high discharges during snowmelt. Old groundwater carbon contributed to stream DOC during the summer drought, although the yield was negligible. However, in a four-week summer precipitation event DOC aged at between 160 and 270 years was delivered into the watershed. In one stream, the DOC was modern but depleted in radiocarbon compared to other hydrological conditions. The yield was substantial and corresponded to 20 to 52% of the annual DOC yields in wet and dry years, respectively. Time-integrating samples of a downstream reservoir also revealed modern DOC ages under moderate conditions and old DOC from the rainfall event. Earlier studies suggested that increasing precipitation escalates the contribution of modern DOC from topsoil layers to surface runoff. Our results demonstrate a step change occurring if rainfall intensities increase and become extreme; then the consequences lead to the mobilization of old carbon in exceptionally high concentrations. The runoff/precipitation ratios of rainfall events indicated that during extreme events upland areas of the catchments were hydrologically connected to the stream and upland DOC was activated. Furthermore, the analysis of long-term data suggested that the DOC export in extreme precipitation events added to the annual yield and was not compensated for by lower exports in remaining periods. We conclude that climate change, along with additional processes associated with human activities, channels old soil carbon into more rapidly cycled carbon pools of the hydrosphere.

Dissolved inorganic and organic carbon yields and fluxes in a permafrost catchment on the Qinghai-Tibet Plateau

NASA Astrophysics Data System (ADS)

Wang, G.; Mao, T.; Zhang, T.; Chen, X.

2015-12-01

Riverine transport of carbon from terrestrial to the aquatic ecosystems is an important component of the global carbon cycle. A warming climate can inevitably accelerate the microbial breakdown of organic carbon and the release of carbon dioxide especially in frozen soils (permafrost) within Arctic and sub-Arctic regions. In addition, high hydraulic conductivity and low sorption capacity of the shallow soil active layer overlying impermeable permafrost together lead to quick DOM transport to streams. In different regions, the response of dissolved carbon to climate warming is different due to the differences in hydrology, climatic conditions, soil types, vegetation conditions, permafrost distribution, catchment size, flow paths. The Qinghai-Tibet Plateau (QTP), of which a significant portion is underlain by permafrost, is considered to be more sensitive to climatic warming than other regions. However, the knowledge of dissolved inorganic and organic carbon transport in the QTP is very limited. We compared the yields and fluxes of DIC/DOC in a small tropical permafrost catchment. Our results showed that: (1) the concentrations ranged from 7.8 to 30.9 mg L-1 for the DIC and ranged from 2.3 to 6.4 mg L-1 for the DOC, the ratio of DIC/DOC concentrations ranged from 2.2 to 5.7 with a mean value of 4.3; (2) the annual export approximately 3.56 t km-2 year-1 for the DIC and 0.73 t km-2 year-1 for the DOC, indicating that the dissolved carbon transported in majority under the inorganic form; (3) the seasonal variations in DIC/DOC export are strongly regulated by variability in runoff, meanwhile the concentration of DIC/DOC showed significant positive correlation with the thawing depth of the active layer and vegetation coverage. Our results provided an understanding about the characteristics of riverine dissolved carbons transport at a permafrost catchment scale on the QTP.

The effect of surface-groundwater interaction on dissolved organic carbon transformation

NASA Astrophysics Data System (ADS)

De Falco, Natalie; Boano, Fulvio; Arnon, Shai

2014-05-01

The preservation and improvement of water quality in streams is a challenging task, limited by our partial understanding of the coupling between biogeochemical and hydrological processes occurring in stream ecosystems. High potential for biogeochemical activity is found in the hyporheic zone, the saturated sediments where surface water and ground water mixes and degradation activities occur. The aim of the study was to quantifythe effect of losing and gaining flow conditions on the degradation of dissolved organic carbon (DOC). Experiments were conducted in a recirculating flume that is equipped with a drainage system that enables the control on losing and gaining fluxes. The degradation of DOC under losing and gaining conditions was studied by spiking the water with benzoic acid and monitoring the decrease in DOC concentration in the bulk water over time using an online UV/Vis spectrophotometer. In addition, the spatial and temporal change in oxygen concentrations within the benthic biofilm was measured using a Clark-type oxygen microelectrode. Preliminary results showed that DOC degradation rate was faster under higher overlying water velocity, due to enhanced delivery of DOC to the biofilm. Under both gaining and losing conditions, the DOC degradation was slower than under neutral condition, probably as a consequence of the reduction of the hyporheic exchange zone. Series of oxygen profiles under losing conditions showed a complete depletion of oxygen within the first 3 millimeters of sediment. In contrast, oxygen profiles under gaining condition showed a incomplete consumption of oxygen (usually within 1 mm), followed by an increase in the concentration of oxygen deeper in the sediments due to the upward flow of oxygenated groundwater. The results suggest that the size of the active aerobic region within the hyporheic zone is changing dynamically with the flow conditions. The effect of flow conditions on redox zonation in the hyporheic zone is expected to affect a myriad of important reactions and ecological processes and should be incorporated on future models.

In Situ Stoichiometry in a Large River: Continuous Measurement of Doc, NO3 and PO4 in the Sacramento River

NASA Astrophysics Data System (ADS)

Downing, B. D.; Pellerin, B. A.; Bergamaschi, B. A.; Saraceno, J.

2011-12-01

Studying controls on geochemical processes in rivers and streams is difficult because concentration and composition often changes rapidly in response to physical and biological forcings. Understanding biogeochemical dynamics in rivers will improve current understanding of the role of watershed sources to carbon cycling, river and stream ecology, and loads to estuaries and oceans. Continuous measurements of dissolved organic carbon (DOC), nitrate (NO3-) and soluble reactive phosphate (SRP) concentrations are now possible, along with some information about DOC composition. In situ sensors designed to measure these constituents provide high frequency, real-time data that can elucidate hydrologic and biogeochemical controls which are difficult to detect using more traditional sampling approaches. Here we present a coupled approach, using in situ optical instrumentation with discharge measurements to provide quantitative estimates of constituent loads to investigate C, NO3- and SRP sources and processing in the Sacramento River, CA, USA. Continuous measurement of DOC concentration was conducted by use of a miniature in situ fluorometer (Turner Designs Cyclops) designed to measure chromophoric dissolved organic matter fluorescence (FDOM) over the course of an entire year. Nitrate was measured concurrently using a Satlantic SUNA and phosphate was measured using a WETLabs model Cycle-P instrument for a two week period in July 2011. Continuous measurement from these instruments paired with continuous measurement of physical water quality variables such as temperature, pH, specific conductance, dissolved oxygen, and turbidity, were used to investigate physical and chemical dynamics of DOC, NO3-, SRP over varying time scales. Deploying these instruments at pre-existing USGS discharge gages allowed for calculation of instantaneous and integrated constituent fluxes, as well as filling in gaps in our understanding biogeochemical processes and transport. Results from the study show that diurnal, event driven and seasonal changes are key to calculating accurate watershed fluxes and detecting transient sources of DOC, NO3- and SRP.

Characterization of dissolved organic matter in an urbanized estuary located in Northeastern Brazil.

PubMed

Arguelho, Maria de Lara Palmeira de Macedo; Alves, José do Patrocínio Hora; Monteiro, Adnívia Santos Costa; Garcia, Carlos Alexandre Borges

2017-06-01

The Sal River estuary, which is located in the state of Sergipe, Northeastern Brazil, stands out as an urban estuary, anthropogenically impacted by untreated and treated wastewater discharge. Synchronous fluorescence spectroscopy and measurement of dissolved organic carbon (DOC) were used for characterization of dissolved organic matter (DOM) in the estuarine water. Dissolved organic carbon concentrations ranged from 7.5 to 19.0 mg L -1 and, in general, the highest values were recorded during dry season. For both seasons (dry and rainy), DOC presented an inverse linear relationship with salinity, which indicates a conservative dilution of organic matter coming into the estuary. During rainy season, anthropogenic organic constituents and humic substances from land-based sources predominated in DOM composition, carried by river flow. Whereas during the dry season, it has been observed a significant increase of products generated by microbial degradation of anthropogenic organic matter. The relationships between fluorescence intensity and salinity suggest a conservative behavior during rainy season and a non-conservative behavior during dry season, with addition of fluorescent organic matter into the intermediate zone of the estuary. Photodegradation by action of sunlight caused a decrease in fluorescence intensity of humic and tryptophan-like constituents and the release of photoproducts, resulting in an increase in fluorescence intensity of protein-like constituents.

Tracking Changes in Dissolved Organic Matter Patterns in Perennial Headwater Streams Throughout a Hydrologic Year Using In-situ Sensors and Optical Properties

NASA Astrophysics Data System (ADS)

Armstrong, A.; Epting, S.; Hosen, J. D.; Palmer, M.

2015-12-01

Dissolved organic matter (DOM) plays a central role in freshwater streams but key questions remain unanswered about temporal patterns in its quantity and composition. DOM in perennial streams in the temperate zone is a complex mixture reflecting a variety of sources such as leached plant material, organic matter from surrounding soils, and microbial processes in the streams themselves. Headwater perennial streams in the Tuckahoe Creek watershed of the Atlantic coastal plain (Maryland, USA) drain a mosaic of land cover types including row crops, forests, and both forested and marshy small depressional wetlands. Wetland-stream surface hydrologic connections generally occur between mid-fall and late spring, coinciding with peak wetland hydrologic expression (i.e. highest groundwater levels and surface inundation extent). When inundated, these wetlands contain high DOM concentrations, and surface connections may serve as conduits for downstream export. We hypothesized that changes in wetland-stream surface hydrologic connectivity would affect patterns of DOM concentration and composition in these streams. We deployed 6 sondes equipped with fluorescent DOM sensors in 4 perennial streams, 1 forested wetland, and the larger downstream channel draining all study sites for the 2015 water year. The 4 headwater streams drain areas containing forested wetlands and have documented temporary channel connections. Combined with baseflow and stormflow sampling, the sondes provided 15 minute estimates of dissolved organic carbon (DOC) concentrations. This resolution provided insights into patterns of DOC concentration across temporal scales from daily rhythms to seasonal changes, during both baseflow and storm conditions. Discrete measurements of absorbance and fluorescence provided information about DOM composition throughout the study. Together these measurements give a detailed record of DOM dynamics in multiple perennial headwater streams for an entire year. This information could inform future studies, such as investigations into stream network scale thresholds in DOM cycling, carbon cycling modelling for the study region, or understanding the impact of wetlands sometimes considered geographically isolated on downstream ecosystems.

Long-term observation of water-soluble chemical components in the bulk atmospheric aerosols collected at Okinawa, Japan

NASA Astrophysics Data System (ADS)

Handa, Daishi; Somada, Yuka; Ijyu, Moriaki; Azechi, Sotaro; Nakaema, Fumiya; Arakaki, Takemitsu; Tanahara, Akira

2010-05-01

The economic development and population growth in recent Asia spread air pollution. Emission rate of air pollutants from Asia, in particular oxides of nitrogen, surpassed those from North America and Europe and should continue to exceed them for decades. The study of the long-range transported air pollution from Asian continent has gained a special attention in Japan because of increase in photochemical oxidants in relatively remote islands. Okinawa Island is situated approximately 1500 km south of Tokyo, Japan, 2000 km southeast of Beijing, China, and 1000 km south of South Korea. Its location in Asia is well suited for studying long-range transport of air pollutants in East Asia because maritime air mass prevails during summer, while continental air mass dominates during fall, winter, and spring. The maritime air mass data can be seen as background and can be compared with continental air masses which have been affected by anthropogenic activities. Bulk aerosol samples were collected on quartz filters by using a high volume air sampler. Sampling duration was one week for each sample. We determined the concentrations of water-soluble anions, cations and dissolved organic carbon (DOC) in the bulk aerosols collected at the Cape Hedo Atmosphere and Aerosol Monitoring Station (CHAAMS) using ion chromatography, atomic absorption spectrometry, and total organic carbon analyzer, respectively. We will report water-soluble chemical components data of anions, cations and DOC in bulk atmospheric aerosols collected at CHAAMS during August, 2005 to April, 2010. Seasonal variation of water-soluble chemical components showed that the concentrations were relatively low in summer, higher in fall and winter, and the highest in spring. When air mass came from Asian Continent, the concentrations of water-soluble chemical components were much higher compared to the other directions. In addition, we calculated background concentration of water-soluble chemical components at Okinawa, Japan.

An intercomparison of three methods for the large-scale isolation of oceanic dissolved organic matter

USGS Publications Warehouse

Green, Nelson W.; Perdue, E. Michael; Aiken, George R.; Butler, Kenna D.; Chen, Hongmei; Dittmar, Thorsten; Niggemann, Jutta; Stubbins, Aron

2014-01-01

Dissolved organic matter (DOM) was isolated from large volumes of deep (674 m) and surface (21 m) ocean water via reverse osmosis/electrodialysis (RO/ED) and two solid-phase extraction (SPE) methods (XAD-8/4 and PPL) at the Natural Energy Laboratory of Hawaii Authority (NELHA). By applying the three methods to common water samples, the efficiencies of XAD, PPL and RO/ED DOM isolation were compared. XAD recovered 42% of dissolved organic carbon (DOC) from deep water (25% with XAD-8; 17% with XAD-4) and 30% from surface water (16% with XAD-8; 14% with XAD-4). PPL recovered 61 ± 3% of DOC from deep water and 61% from surface water. RO/ED recovered 82 ± 3% of DOC from deep water, 14 ± 3% of which was recovered in a sodium hydroxide rinse, and 75 ± 5% of DOC from surface water, with 12 ± 2% in the sodium hydroxide rinse. The highest recoveries of all were achieved by the sequential isolation of DOC, first with PPL and then via RO/ED. This combined technique recovered 98% of DOC from a deep water sample and 101% of DOC from a surface water sample. In total, 1.9, 10.3 and 1.6 g-C of DOC were collected via XAD, PPL and RO/ED, respectively. Rates of DOC recovery using the XAD, PPL and RO/ED methods were 10, 33 and 10 mg-C h− 1, respectively. Based upon C/N ratios, XAD isolates were heavily C-enriched compared with water column DOM, whereas RO/ED and PPL ➔ RO/ED isolate C/N values were most representative of the original DOM. All techniques are suitable for the isolation of large amounts of DOM with purities suitable for most advanced analytical techniques. Coupling PPL and RO/ED techniques may provide substantial progress in the search for a method to quantitatively isolate oceanic DOC, bringing the entirety of the DOM pool within the marine chemist's analytical window.

Precipitation regime effects on the transport of microbial-derived organic matter from soils to surface waters

NASA Astrophysics Data System (ADS)

Pissarello, Anna; Lechtenfeld, Oliver; Miltner, Anja; Kästner, Matthias

2017-04-01

In the last decades, decreases in soil organic matter (SOM) content and increases of dissolved organic carbon (DOC) concentrations in surface water bodies have been recorded in the northern hemisphere. These have severe consequences for soil fertility and for drinking water purification, respectively. We hypothesize that microbially degraded SOM is a potential source of the additional DOC in the surface water. Recently, rain events have become more extreme, resulting in longer droughts and more intense rain events. These changes in the precipitation regime may increase the input of DOC into surface waters, which occurs mainly directly after heavy rain events. Therefore, our interest was to evaluate the role of variations of the water regime on the mobilization of the DOC from soil organic matter to soil solution. Flow-through column experiments were conducted under extreme precipitation scenarios (from continuously wet to pronounced drying and rewetting) in the laboratory in order to test how fluctuation in the water content influences DOC concentration and composition in the leachates. In our experiment we analyzed both soil respiration and DOM mobilization and found that the increased DOM mobilization after heavy rain events was also an effect of increased microbial activity after the drought stress was relieved. Furthermore, we considered that an important contribution to DOC formation and export may come from microbial processing of microbial biomass residues, residing within the particulate organic matter (POM) fraction. Therefore our aim was to link the necromass contribution to the exported DOC by characterizing DOC leachates of the soil columns at the molecular level and comparing them to fractions of bacterial DOC and POC obtained from an Escherichia coli pure culture, by using ultra-high-resolution methods such as Electrospray Ionization and Matrix assisted laser desorption/ionization Fourier transform ion cyclotron resonance mass spectrometry (ESI-FTICR-MS and MALDI-FTICR-MS, respectively). The results help to relate the origin of organic matter to typical chemical composition patterns and to allow quantification of the relative contributions of plant and microbe-derived material to NOM and how they are affected by the different water regimes. The results of this experiment consent to link SOM degradation and DOC mobilization and to understand the role of water regime variations for these processes.

High soil solution carbon und nitrogen concentrations in a drained Atlantic bog are reduced to natural levels by 10 yr of rewetting

NASA Astrophysics Data System (ADS)

Frank, S.; Tiemeyer, B.; Gelbrecht, J.; Freibauer, A.

2013-10-01

Artificial drainage of peatlands causes dramatic changes in the release of greenhouse gases and in the export of dissolved carbon (C) and nutrients to downstream ecosystems. Rewetting anthropogenically altered peatlands offers a possibility to reduce nitrogen (N) and C losses. In this study, we investigate the impact of drainage and rewetting on the cycling of dissolved C and N as well as on dissolved gases over a period of 1 yr and 4 month, respectively. The peeper technique was used to receive a high vertical sampling resolution. Within one Atlantic bog complex a near natural site, two drained grasslands sites with different mean water table positions, and a former peat cutting area rewetted 10 yr ago were chosen. Our results clearly indicate that drainage increased the concentration of dissolved organic carbon (DOC), ammonia, nitrate and dissolved organic nitrogen (DON) compared to the near natural site. Drainage depth further determined the release and therefore the concentration level of DOC and N species, but the biochemical cycling and therefore dissolved organic matter (DOM) quality and N species composition were unaffected. Thus, especially deep drainage can cause high DOC losses. In general, DOM at drained sites was enriched in aromatic moieties as indicated by SUVA280 and showed a higher degradation status (lower DOC to DON ratio) compared to the near natural site. At the drained sites, equal C to N ratios of uppermost peat layer and DOC to DON ratio of DOM in soil solution suggest that the uppermost degraded peat layer is the main source of DOM. Nearly constant DOC to DON ratios and SUVA280 values with depth furthermore indicated that DOM moving downwards through the drained sites remained largely unchanged. DON and ammonia contributed most to the total dissolved nitrogen (TN). The subsoil concentrations of nitrate were negligible due to strong decline in nitrate around mean water table depth. Methane production during the winter months at the drained sites moved downwards to areas which were mostly water saturated over the whole year (>40 cm). Above these depths, the recovery of the water table in winter months led to the production of nitrous oxide around mean water table depth at drained sites. 10 yr after rewetting, the DOM quality (DOC to DON ratio and SUVA280) and quantity were comparable to the near natural site, indicating the re-establishment of mostly pristine biochemical processes under continuously water logged conditions. The only differences occur in elevated dissolved methane and ammonia concentrations reflecting the former disturbance by drainage and peat extraction. Rewetting via polder technique seems to be an appropriate way to revitalize peatlands on longer timescales and to improve the water quality of downstream water bodies.

Seasonal changes in particulate and dissolved organic matter composition and quality in the Lena River Delta

NASA Astrophysics Data System (ADS)

Mollenhauer, G.; Winterfeld, M.; Hefter, J.; Bodenstab, L.; Morgenstern, A.; Eulenburg, A.; Heim, B.; Koch, B.; Schefuss, E.; Moerth, C. M.; Rethemeyer, J.

2016-12-01

Arctic rivers are known to export large quantities of carbon by discharge of dissolved and particulate organic carbon (DOC, POC), and in a warming and progressively moister Arctic, these exports may increase resulting in a reduction of arctic continental carbon stocks. These rivers have highly variable discharge rates with a pronounced maximum during the spring freshet associated with highest concentrations of DOC and POC. Most studies investigating the isotopic composition and quality of carbon exported by Arctic rivers rely on samples taken in summer during base flow, which is due to the logistical challenges associated with sampling in the remote Arctic permafrost regions. Here we present a record of δ13C and Δ14C of DOC and POC collected between late May during the freshet and late August 2014 in the Lena River Delta. POC Δ14C shows an initial trend towards older values in the spring samples, which is reversed in summer, associated with a shift towards more depleted δ13C values. We interpret this aging trend as reflecting progressive thawing throughout the ice-free season, resulting in mobilization of progressively older carbon from deeper thawed layers. The summer reversal indicates admixture of aquatic organic matter. DOC Δ14C, in contrast, remains at relatively modern levels with rather constant δ13C values throughout the sampling period. We furthermore analysed the biomarker composition of Lena Delta particulate OM collected in spring and summer. From spring to summer, we observe trends in abundance of individual leaf-wax derived biomarkers indicating higher abundance of algal biomass in the summer particles. Trends in soil microbial biomarkers and compound-specific δD of leaf-wax lipids suggest a shift in sources towards higher contributions from the southern catchment in summer. DOC composition investigated with FT-ICR-MS changes from spring with higher abundances of compounds with high H/C and low O/C ratios to late summer, when fewer compounds were found. Our results illustrate the seasonal variability in composition and sources of organic matter discharged by the Lena River. Paired with the strong seassonality of the hydrograph, this implies that total annual discharge of organic matter contains a disproportionally high contribution from the northern part of the catchment.

Spatial and temporal variation in dissolved organic carbon composition in a peaty catchment draining a windfarm

NASA Astrophysics Data System (ADS)

Zheng, Ying; Waldron, Susan; Flowers, Hugh

2015-04-01

Peatlands are an important terrestrial carbon reserve and a principal source of dissolved organic carbon (DOC) to the fluvial environment (Wallage et al. 2006). Recently it has been observed that DOC concentrations [DOC] in surface waters have increased in Europe and North America (Monteith et al. 2007). This has been attributed primarily to reduced acid deposition. However, land use change can also release C from peat soils. A significant land use change in Scotland is hosting windfarms. Whether windfarm construction causes such impacts has been a research focus, particularly considering fluvial losses, but usually assessing if there are changes in DOC concentration rather than composition. Our study area is a peaty catchment that hosts wind turbines, has peat restoration activities and forest felling and is drained by two streams. We are using UV-visible and fluorescence spectrophotometry to assess if there are differences between the two steams or temporal changes in DOC composition. We will present data from samples collected since February 2014. The parameters we are focusing on are SUVA254, E4/E6 and E2/E4 ratios as these are indicators of DOC aromaticity, humic acid (HA): fulvic acid (FA) ratio and the proportion of humic substances in DOC (Weishaar, 2003; Spencer et al. 2007; Graham et al. 2012). To assess these we have measured UV-visible absorbance spectra from 200 nm to 800 nm. Meanwhile sample fluorescence emission and excitation matrix (EEM) will be applied with the PARAFAC model to obtain more information about the variations in humic substances in this catchment. Our current analysis indicates spatial differences not only in DOC concentration but also in composition. For example, the mainstem draining the windfarm area had a smaller [DOC] but higher E4/E6 and lower E2/E4 ratio values than the tributary draining an area of felled forestry. This may be indicative of more HAs in the mainstem DOC. Seasonal variations have also been observed. Both streams had high [DOC] in summer and autumn compared to spring. While E2/E4 ratios were steady in both streams, a more variable E4/E6 ratio in the mainstem may suggest DOC composition changed more over time than in the tributary which had a relatively stable E4/E6 ratio. [DOC] fell in both streams during the summer drought period but a corresponding fall in SUVA254 in the mainstem but not the tributary is further evidence of differences in DOC composition between the two streams. Such spatial and temporal understanding is needed to understand if, and how, land use influences the composition of the DOC exported. References: Graham M. C. et al. 2012. Processes controlling manganese distributions and associations in organic-rich freshwater aquatic systems: The example of Loch Bradan, Scotland. Science of the Total Environment, 424, 239-250. Monteith D. et al. 2007. Dissolved organic carbon trends resulting from changes in atmospheric chemistry. Nature,450, 537-540. Spencer R.G.M, Bolton L. and Baker A. 2007. Freeze/thaw and pH effects on freshwater dissolved organic matter fluorescence and absorbance properties from a number of UK locations.Water Research, 41 (13):2941-2950. Wallage Z.E., Holden, J. and McDonald, A.T. 2006. Drain blocking: An effective treatment for reducing dissolved organic carbon loss and water discolouration in a drained peatland. Science of the total environment, 367, 811-821. Weishaar J.L. et al. 2003. Evaluation of specific ultraviolet absorbance as an indicator of the chemical composition and reactivity of dissolved organic carbon. Environmental Science & Technology 37(20): 4702-4708.

Dissolved organic carbon and chromophoric dissolved organic matter properties of rivers in the USA

NASA Astrophysics Data System (ADS)

Spencer, Robert G. M.; Butler, Kenna D.; Aiken, George R.

2012-09-01

Dissolved organic carbon (DOC) concentration and chromophoric dissolved organic matter (CDOM) parameters were measured over a range of discharge in 30 U.S. rivers, covering a diverse assortment of fluvial ecosystems in terms of watershed size and landscape drained. Relationships between CDOM absorption at a range of wavelengths (a254, a350, a440) and DOC in the 30 watersheds were found to correlate strongly and positively for the majority of U.S. rivers. However, four rivers (Colorado, Colombia, Rio Grande and St. Lawrence) exhibited statistically weak relationships between CDOM absorption and DOC. These four rivers are atypical, as they either drain from the Great Lakes or experience significant impoundment of water within their watersheds, and they exhibited values for dissolved organic matter (DOM) parameters indicative of autochthonous or anthropogenic sources or photochemically degraded allochthonous DOM and thus a decoupling between CDOM and DOC. CDOM quality parameters in the 30 rivers were found to be strongly correlated to DOM compositional metrics derived via XAD fractionation, highlighting the potential for examining DOM biochemical quality from CDOM measurements. This study establishes the ability to derive DOC concentration from CDOM absorption for the majority of U.S. rivers, describes characteristics of riverine systems where such an approach is not valid, and emphasizes the possibility of examining DOM composition and thus biogeochemical function via CDOM parameters. Therefore, the usefulness of CDOM measurements, both laboratory-based analyses and in situ instrumentation, for improving spatial and temporal resolution of DOC fluxes and DOM dynamics in future studies is considerable in a range of biogeochemical studies.

Examining organic carbon transport by the Orinoco River using SeaWiFS imagery

NASA Astrophysics Data System (ADS)

López, Ramón; Del Castillo, Carlos E.; Miller, Richard L.; Salisbury, Joseph; Wisser, Dominik

2012-09-01

The Orinoco River is the fourth largest in the world in terms of water discharge and organic carbon export to the ocean. River export of organic carbon is a key component of the carbon cycle and the global carbon budget. Here, we examined the seasonal transport of organic carbon by the Orinoco River into the eastern Caribbean using the conservative relationship of colored dissolved organic matter (CDOM) and dissolved organic carbon (DOC) in low salinity coastal waters influenced by river plumes. In situ measurements of CDOM absorption, DOC, and salinity were used to develop an empirical model for DOC concentration at the Orinoco River Plume. Satellite remote sensing reflectances were used with empirical models to determine DOC and Particulate organic carbon (POC) river transport. Our estimates of CDOM and DOC significantly correlated with in situ measurements and were within the expected ranges for the river. Total organic carbon transport by the Orinoco River during the period of 1998 to 2010 was 7.10 ×1012 g C y-1, from 5.29 × 1012 g C y-1 of DOC and 1.81 × 1012 g C y-1 of POC, representing ˜6% increase to previous published estimates. The variability in organic carbon transport responded to the seasonality in river flow more than to changes in organic carbon concentration in the river. Our results corroborate that is possible to estimate organic carbon transport using ocean color data at global scales. This is needed to reduce the uncertainties of land-ocean carbon fluxes.

Dissolved organic carbon and chromophoric dissolved organic matter properties of rivers in the USA

USGS Publications Warehouse

Spencer, Robert G.M.; Butler, Kenna D.; Aiken, George R.

2012-01-01

Dissolved organic carbon (DOC) concentration and chromophoric dissolved organic matter (CDOM) parameters were measured over a range of discharge in 30 U.S. rivers, covering a diverse assortment of fluvial ecosystems in terms of watershed size and landscape drained. Relationships between CDOM absorption at a range of wavelengths (a254, a350, a440) and DOC in the 30 watersheds were found to correlate strongly and positively for the majority of U.S. rivers. However, four rivers (Colorado, Colombia, Rio Grande and St. Lawrence) exhibited statistically weak relationships between CDOM absorption and DOC. These four rivers are atypical, as they either drain from the Great Lakes or experience significant impoundment of water within their watersheds, and they exhibited values for dissolved organic matter (DOM) parameters indicative of autochthonous or anthropogenic sources or photochemically degraded allochthonous DOM and thus a decoupling between CDOM and DOC. CDOM quality parameters in the 30 rivers were found to be strongly correlated to DOM compositional metrics derived via XAD fractionation, highlighting the potential for examining DOM biochemical quality from CDOM measurements. This study establishes the ability to derive DOC concentration from CDOM absorption for the majority of U.S. rivers, describes characteristics of riverine systems where such an approach is not valid, and emphasizes the possibility of examining DOM composition and thus biogeochemical function via CDOM parameters. Therefore, the usefulness of CDOM measurements, both laboratory-based analyses and in situ instrumentation, for improving spatial and temporal resolution of DOC fluxes and DOM dynamics in future studies is considerable in a range of biogeochemical studies.

Flux and Seasonality of Dissolved Organic Matter From the Northern Dvina (Severnaya Dvina) River, Russia

NASA Astrophysics Data System (ADS)

Johnston, Sarah Ellen; Shorina, Natalia; Bulygina, Ekaterina; Vorobjeva, Taisya; Chupakova, Anna; Klimov, Sergey I.; Kellerman, Anne M.; Guillemette, Francois; Shiklomanov, Alexander; Podgorski, David C.; Spencer, Robert G. M.

2018-03-01

Pan-Arctic riverine dissolved organic carbon (DOC) fluxes represent a major transfer of carbon from land-to-ocean, and past scaling estimates have been predominantly derived from the six major Arctic rivers. However, smaller watersheds are constrained to northern high-latitude regions and, particularly with respect to the Eurasian Arctic, have received little attention. In this study, we evaluated the concentration of DOC and composition of dissolved organic matter (DOM) via optical parameters, biomarkers (lignin phenols), and ultrahigh resolution mass spectrometry in the Northern Dvina River (a midsized high-latitude constrained river). Elevated DOC, lignin concentrations, and aromatic DOM indicators were observed throughout the year in comparison to the major Arctic rivers with seasonality exhibiting a clear spring freshet and also some years a secondary pulse in the autumn concurrent with the onset of freezing. Chromophoric DOM absorbance at a350 was strongly correlated to DOC and lignin across the hydrograph; however, the relationships did not fit previous models derived from the six major Arctic rivers. Updated DOC and lignin fluxes were derived for the pan-Arctic watershed by scaling from the Northern Dvina resulting in increased DOC and lignin fluxes (50 Tg yr-1 and 216 Gg yr-1, respectively) compared to past estimates. This leads to a reduction in the residence time for terrestrial carbon in the Arctic Ocean (0.5 to 1.8 years). These findings suggest that constrained northern high-latitude rivers are underrepresented in models of fluxes based from the six largest Arctic rivers with important ramifications for the export and fate of terrestrial carbon in the Arctic Ocean.

Climate and landscape influence on indicators of lake carbon cycling through spatial patterns in dissolved organic carbon.

PubMed

Lapierre, Jean-Francois; Seekell, David A; Del Giorgio, Paul A

2015-12-01

Freshwater ecosystems are strongly influenced by both climate and the surrounding landscape, yet the specific pathways connecting climatic and landscape drivers to the functioning of lake ecosystems are poorly understood. Here, we hypothesize that the links that exist between spatial patterns in climate and landscape properties and the spatial variation in lake carbon (C) cycling at regional scales are at least partly mediated by the movement of terrestrial dissolved organic carbon (DOC) in the aquatic component of the landscape. We assembled a set of indicators of lake C cycling (bacterial respiration and production, chlorophyll a, production to respiration ratio, and partial pressure of CO2 ), DOC concentration and composition, and landscape and climate characteristics for 239 temperate and boreal lakes spanning large environmental and geographic gradients across seven regions. There were various degrees of spatial structure in climate and landscape features that were coherent with the regionally structured patterns observed in lake DOC and indicators of C cycling. These different regions aligned well, albeit nonlinearly along a mean annual temperature gradient; whereas there was a considerable statistical effect of climate and landscape properties on lake C cycling, the direct effect was small and the overall effect was almost entirely overlapping with that of DOC concentration and composition. Our results suggest that key climatic and landscape signals are conveyed to lakes in part via the movement of terrestrial DOC to lakes and that DOC acts both as a driver of lake C cycling and as a proxy for other external signals. © 2015 John Wiley & Sons Ltd.

Removal of micropollutants from Sakarya River water by ozone and membrane processes.

PubMed

Yaman, Fatma Büşra; Çakmakcı, Mehmet; Yüksel, Ebubekir; Özen, İsmail; Gengeç, Erhan

2017-09-01

The removal of some pollutants in the Sakarya River was investigated in this study. Sakarya River located in Turkey flows from the northeast of Afyonkarahisar City to the Black Sea. Nineteen different micropollutants including trihalomethanes (THMs), haloacetic acids (HAAs), endocrine disrupting compound (EDC) and pharmaceuticals personal care product (PPCP) groups, and water quality parameters such as dissolved organic carbon (DOC), ultraviolet absorbance at 254 nm wavelength (UV 254 ), hardness, and conductivity values were examined. To remove the micropollutants and improve the water quality, the treatment was performed with ozone, microfiltration (MF), and ultra-filtration (UF) membranes. The highest treatment efficiency was obtained with 1 mg/L ozone dosage and UP005 UF membrane. The trihalomethan formation potential (THMFP) and haloacetic acid formation potential (HAAFP) decreased with ozone + membrane at a concentration of 79 and 75%, respectively. After the treatment with ozone + membrane, the concentration of the micropollutants in the EDC and PPCP group remained below the detection limit. It was found that by using only membrane and only ozone, the maximum DOC removal efficiency achieved was 46 and 18%, respectively; and with ozone + membrane, this efficiency increased up to 82%. The results from the High-Pressure Size Exclusion Chromatography (HPSEC) analyses pointed that the substances with high molecular weight were converted into substances with low molecular weight after the treatment. The Fourier Transform Infrared (FTIR) analysis results showed that the aromatic and aliphatic functional groups in water changed after the treatment with ozone and that the peak values decreased more after the ozone + membrane treatment.

Impact of diatom growth on trace metal dynamics (Mn, Mo, V, U)

NASA Astrophysics Data System (ADS)

Osterholz, Helena; Simon, Heike; Beck, Melanie; Maerz, Joeran; Rackebrandt, Siri; Brumsack, Hans-Jürgen; Feudel, Ulrike; Simon, Meinhard

2014-03-01

In order to examine the specific role of diatoms in cycling of the trace metals manganese (Mn), molybdenum (Mo), vanadium (V), and uranium (U) Thalassiosira rotula, Skeletonema marinoi, Chaetoceros decipiens, and Rhizosolenia setigera were grown in batch cultures axenically and inoculated with three different bacterial strains isolated from the North Sea. Algal and bacterial growth, concentrations of trace metals and dissolved organic carbon (DOC) were monitored over time and showed that Mn and V were removed from the dissolved phase whereas Mo and U were not. R. setigera and T. rotula exhibited lowest growth and lowest removal whereas S. marinoi grew best and removed highest fractions of Mn and V. The high potential of Mn removal by S. marinoi was also evident from its 7 × higher Mn/P elemental ratio relative to T. rotula. The presence of bacteria modified the timing of the growth of S. marinoi but not directly trace metal removal whereas bacteria enhanced trace metal removal in the cultures of T. rotula and C. decipiens. Modeling of phytoplankton growth, concentrations of Mn and DOC fraction in axenic T. rotula cultures indicated that processes of binding and desorption of Mn to excreted organic components are important to explain the varying proportions of dissolved Mn and thus must be considered as an active component in Mn cycling. The results show distinct differences in the potential of the diatoms in the removal of Mn and V and that bacteria can play an active role in this context. S. marinoi presumably is an important player in Mn and V dynamics in coastal marine systems.

The influence of precursors and treatment process on the formation of Iodo-THMs in Canadian drinking water.

PubMed

Tugulea, Anca-Maria; Aranda-Rodriguez, Rocio; Bérubé, Denis; Giddings, Michèle; Lemieux, France; Hnatiw, Joan; Dabeka, Luda; Breton, François

2018-03-01

The National Survey of Disinfection By-Products and Selected Emerging Contaminants investigated the formation of various disinfection by-products and contaminants in 65 water treatment systems (WTSs) across Canada. Results for six iodo-trihalomethanes (iodo-THMs) are reported in this paper. The participating water treatment systems included large, medium and small systems using water sources and treatment processes which were representative of Canadian drinking water. Five water samples (source water, treated water and three water samples along the distribution system) were collected from each treatment system, both under winter and summer conditions. Samples were stabilized, shipped cold and analysed for six iodo-THMs (dichloroiodomethane-DCIM; dibromoiodomethane-DBIM; bromochloroiodomethane-BCIM; chlorodiiodomethane-CDIM; bromodiiodomethane-BDIM and triiodomethane or iodoform-TIM), using a SPME-GC-ECD method developed in our laboratory (MDLs from 0.02 μg/L for iodoform to 0.06 μg/L for bromodiiodomethane). Concentrations of relevant precursors like dissolved organic carbon (DOC), bromide, iodide and total iodine, as well as other water quality parameters, were also determined. Detailed information about the treatment process used at each location was recorded using a questionnaire. The survey showed that one or more iodo-THMs were detected at 31 out of 64 water treatment systems (WTSs) under winter conditions and in 46 out of 64 WTSs under summer conditions (analytical results from one site were excluded due to sampling challenges). Total iodo-THM concentrations measured during this survey ranged from 0.02 μg/L to 21.66 μg/L. The highest total iodo-THM concentration was measured in WTS 63 where all six iodo-THMs were detected and iodoform was present in the highest concentration. The highest iodo-THM formation was found to occur in treatment systems where water sources had naturally occurring ammonium as well as high bromide, high iodide and/or total iodine concentrations. In two such water systems the total concentration of iodo-THMs exceeded the concentration of regulated THMs. Copyright © 2017. Published by Elsevier Ltd.

A comparison of four porewater sampling methods for metal mixtures and dissolved organic carbon and the implications for sediment toxicity evaluations.

PubMed

Cleveland, Danielle; Brumbaugh, William G; MacDonald, Donald D

2017-11-01

Evaluations of sediment quality conditions are commonly conducted using whole-sediment chemistry analyses but can be enhanced by evaluating multiple lines of evidence, including measures of the bioavailable forms of contaminants. In particular, porewater chemistry data provide information that is directly relevant for interpreting sediment toxicity data. Various methods for sampling porewater for trace metals and dissolved organic carbon (DOC), which is an important moderator of metal bioavailability, have been employed. The present study compares the peeper, push point, centrifugation, and diffusive gradients in thin films (DGT) methods for the quantification of 6 metals and DOC. The methods were evaluated at low and high concentrations of metals in 3 sediments having different concentrations of total organic carbon and acid volatile sulfide and different particle-size distributions. At low metal concentrations, centrifugation and push point sampling resulted in up to 100 times higher concentrations of metals and DOC in porewater compared with peepers and DGTs. At elevated metal levels, the measured concentrations were in better agreement among the 4 sampling techniques. The results indicate that there can be marked differences among operationally different porewater sampling methods, and it is unclear if there is a definitive best method for sampling metals and DOC in porewater. Environ Toxicol Chem 2017;36:2906-2915. Published 2017 Wiley Periodicals Inc. on behalf of SETAC. This article is a US government work and, as such, is in the public domain in the United States of America. Published 2017 Wiley Periodicals Inc. on behalf of SETAC. This article is a US government work and, as such, is in the public domain in the United States of America.

Seasonal and event-scale controls on dissolved organic carbon and nitrate flushing from catchments

NASA Astrophysics Data System (ADS)

Sebestyen, S. D.; Boyer, E. W.; Shanley, J. B.; Doctor, D. H.

2005-05-01

To explore terrestrial and aquatic linkages controlling nutrient dynamics in forested catchments, we collected high-frequency samples from 2002 to 2004 at the Sleepers River Research Watershed in northeastern Vermont USA. We measured DOC (dissolved organic carbon), SUVA (specific UV absorbance), nitrate, and major ion concentrations over a wide range of flow conditions. In addition, weekly samples since 1991 provide a longer term record of stream nutrient fluxes. During events, DOC concentrations increased with flow consistent with the flushing of a large reservoir of mobile organic carbon from forest soils. Higher concentrations of DOC and SUVA in the growing versus dormant season illustrated seasonal variation in sources, characteristics (i.e. reactivity), availability, and controls on the flushing response of organic matter from the landscape to streams. In contrast, stream nitrate concentrations increased with flow but only when catchments "wetted-up" after baseflow periods. Growing season stream nitrate responses were dependent on short-term antecedent moisture conditions indicating rapid depletion of the soil nitrate reservoir when source areas became hydrologically connected to streams. While the different response patterns emphasized variable source and biogeochemical controls in relation to flow patterns, coupled carbon and nitrogen biogeochemical processes were also important controls on stream nutrient fluxes. In particular, leaf fall was a critical time when reactive DOC from freshly decomposing litter fueled in-stream consumption of nitrate leading to sharp declines of stream nitrate concentrations. Our measurements highlight the importance of "hot spots" and "hot moments" of biogeochemical and hydrological processes that control stream responses. Furthermore, our work illustrates how carbon, nitrogen, and water cycles are coupled in catchments, and provides a conceptual model for future work aimed at modeling forest stream hydrochemistry at the catchment scale.

Catchment influence on nitrate and dissolved organic matter in Alaskan streams across a latitudinal gradient

DOE PAGES

Harms, Tamara K.; Edmonds, Jennifer W.; Genet, Hélène; ...

2016-01-10

Spatial patterns in carbon (C) and nitrogen (N) cycles of high-latitude catchments have been linked to climate and permafrost and used to infer potential changes in biogeochemical cycles under climate warming. However, inconsistent spatial patterns across regions indicate that factors in addition to permafrost and regional climate may shape responses of C and N cycles to climate change. In this paper, we hypothesized that physical attributes of catchments modify responses of C and N cycles to climate and permafrost. We measured dissolved organic C (DOC) and nitrate (NO 3 ¯) concentrations, and composition of dissolved organic matter (DOM) in 21more » streams spanning boreal to arctic Alaska, and assessed permafrost, topography, and attributes of soils and vegetation as predictors of stream chemistry. Multiple regression analyses indicated that catchment slope is a primary driver, with lower DOC and higher NO 3 ¯ concentration in streams draining steeper catchments, respectively. Depth of the active layer explained additional variation in concentration of DOC and NO 3 ¯. Vegetation type explained regional variation in concentration and composition of DOM, which was characterized by optical methods. Composition of DOM was further correlated with attributes of soils, including moisture, temperature, and thickness of the organic layer. Finally, regional patterns of DOC and NO 3 ¯ concentrations in boreal to arctic Alaska were driven primarily by catchment topography and modified by permafrost, whereas composition of DOM was driven by attributes of soils and vegetation, suggesting that predicting changes to C and N cycling from permafrost-influenced regions should consider catchment setting in addition to dynamics of climate and permafrost.« less

Effects of long-term land use change on dissolved carbon characteristics in the permafrost streams of northeast China.

PubMed

Guo, Yuedong; Song, Changchun; Wan, Zhongmei; Tan, Wenwen; Lu, Yongzheng; Qiao, Tianhua

2014-11-01

Permafrost soils act as large sinks of organic carbon but are highly sensitive to interference such as changes in land use, which can greatly influence dissolved carbon loads in streams. This study examines the effects of long-term land reclamation on seasonal concentrations of dissolved carbons in the upper reaches of the Nenjiang River, northeast China. A comparison of streams in natural and agricultural systems shows that the dissolved organic carbon (DOC) concentration is much lower in the agricultural stream (AG) than in the two natural streams (WAF, wetland dominated; FR, forest dominated), suggesting that land use change is associated with reduced DOC exporting capacity. Moreover, the fluorescence indexes and the ratio of dissolved carbon to nitrogen also differ greatly between the natural and agricultural streams, indicating that the chemical characteristics and the origin of the DOC released from the whole reaches are also altered to some extent. Importantly, the exporting concentration of dissolved inorganic carbon (DIC) and its proportion of total dissolved carbon (TDC) substantially increase following land reclamation, which would largely alter the carbon cycling processes in the downstream fluvial system. Although the strong association between the stream discharge and the DOC concentration was unchanged, the reduction in total soil organic carbon following land reclamation led to remarkable decline of the total flux and exporting coefficient of the dissolved carbons. The results suggest that dissolved carbons in permafrost streams have been greatly affected by changes in land use since the 1970s, and the changes in the concentration and chemical characteristics of dissolved carbons will last until the alteration in both the traditional agriculture pattern and the persistent reclamation activities.

Nonlinear and threshold-dominated runoff generation controls DOC export in a small peat catchment

NASA Astrophysics Data System (ADS)

Birkel, C.; Broder, T.; Biester, H.

2017-03-01

We used a relatively simple two-layer, coupled hydrology-biogeochemistry model to simultaneously simulate streamflow and stream dissolved organic carbon (DOC) concentrations in a small lead and arsenic contaminated upland peat catchment in northwestern Germany. The model procedure was informed by an initial data mining analysis, in combination with regression relationships of discharge, DOC, and element export. We assessed the internal model DOC processing based on stream DOC hysteresis patterns and 3-hourly time step groundwater level and soil DOC data for two consecutive summer periods in 2013 and 2014. The parsimonious model (i.e., few calibrated parameters) showed the importance of nonlinear and rapid near-surface runoff generation mechanisms that caused around 60% of simulated DOC load. The total load was high even though these pathways were only activated during storm events on average 30% of the monitoring time—as also shown by the experimental data. Overall, the drier period 2013 resulted in increased nonlinearity but exported less DOC (115 kg C ha-1 yr-1 ± 11 kg C ha-1 yr-1) compared to the equivalent but wetter period in 2014 (189 kg C ha-1 yr-1 ± 38 kg C ha-1 yr-1). The exceedance of a critical water table threshold (-10 cm) triggered a rapid near-surface runoff response with associated higher DOC transport connecting all available DOC pools and subsequent dilution. We conclude that the combination of detailed experimental work with relatively simple, coupled hydrology-biogeochemistry models not only allowed the model to be internally constrained but also provided important insight into how DOC and tightly coupled pollutants or trace elements are mobilized.

Climatic and chemical drivers of trends in DOC in northern surface waters in Europa and North America

NASA Astrophysics Data System (ADS)

de Wit, Heleen A.; Monteith, Don T.; Stoddard, John L.

2016-04-01

Concentrations of DOC in boreal surface waters have increased to levels that create challenges for water treatment plants, and that potentially impact lake habitat through increased anoxia and thermal mixing, and productivity. Aquatic transport of DOC from land to oceans is likely to increase, even if runoff patterns would remain stable. Reduced acid deposition appears to be a dominant driver behind the increase in DOC concentrations, through increasing organic matter solubility. We hypothesize that the higher solubility of organic matter makes DOC more susceptible to climate change. Here, we present trends in DOC from circa 500 lakes and streams in subarctic, boreal and temperate headwater catchments in Europe (UK, Fennoscandia, Czech Republic, Slovakia) and North America (Northeastern US, Ontario, Atlantic Canada) from 1990 until 2012; an extension of the trend analysis presented in Monteith et al. (2007). The water chemical data stem from national monitoring networks, assembled by the ICP Waters network. Sampling frequencies vary from 1 to 52 samples per year. Climate data were obtained from Climate Research Unit in the UK. Trends were calculated using the Mann-Kendall test and the Sen-slope estimator. We test 1) if DOC responds to changes in the rate of decline in acid deposition, and 2) if trends in temperature and precipitation affect trends and variability in DOC. Positive trends dominate: the median (±2.5% quartile) of the absolute and relative DOC trends is +0.06 (+0.36 to -0.02) mg C L-1 yr-1 and +1.4 (+4.7 to -0.9) % yr-1, respectively. Overall, the trends do not level off when comparing 1990-2004, and 1998-2012, except in the UK and Atlantic Canada. These two regions are strongly impacted by seasalt deposition but may also experience stronger warming than elsewhere. The response of DOC to changes in SO4 (expressed as trend ratios) is stronger in 1998-2012 than in 1990-2004. We will explore whether this changing relates to increasing dominance of drivers, such as temperature or precipitation, and will present multivariate models of DOC trends in relation to climate and deposition. References Monteith DT, Stoddard JL, Evans CD, de Wit HA, Forsius M, Hogasen T, Wilander A, Skjelkvale BL, Jeffries DS, Vuorenmaa J, Keller B, Kopacek J, Vesely J (2007) Dissolved organic carbon trends resulting from changes in atmospheric deposition chemistry. Nature 450(7169): 537-540

Speciation of Se and DOC in soil solution and their relation to Se bioavailability.

PubMed

Weng, Liping; Vega, Flora Alonso; Supriatin, Supriatin; Bussink, Wim; Van Riemsdijk, Willem H

2011-01-01

A 0.01 M CaCl(2) extraction is often used to asses the bioavailability of plant nutrients in soils. However, almost no correlation was found between selenium (Se) in the soil extraction and Se content in grass. The recently developed anion Donnan membrane technique was used to analyze chemical speciation of Se in the 0.01 M CaCl(2) extractions of grassland soils and fractionation of DOC (dissolved organic carbon). The results show that most of Se (67-86%) in the extractions (15 samples) are colloidal-sized Se. Only 13-34% of extractable Se are selenate, selenite and small organic Se (<1 nm). Colloidal Se is, most likely, Se bound to or incorporated in colloidal-sized organic matter. The dominant form of small Se compounds (selenate, selenite/small organic compounds) depends on soil. A total of 47-85% of DOC is colloidal-sized and 15-53% are small organic molecules (<1 nm). In combination with soluble S (sulfur) and/or P (phosphor), concentration of small DOC can explain most of the variability of Se content in grass. The results indicate that mineralization of organic Se is the most important factor that controls Se availability in soils. Competition with sulfate and phosphate needs to be taken into account. Further research is needed to verify if concentration of small DOC is a good indicator of mineralization of soil organic matter.

Reclamation of zinc-contaminated soil using a dissolved organic carbon solution prepared using liquid fertilizer from food-waste composting.

PubMed

Chiang, Po-Neng; Tong, Ou-Yang; Chiou, Chyow-San; Lin, Yu-An; Wang, Ming-Kuang; Liu, Cheng-Chung

2016-01-15

A liquid fertilizer obtained through food-waste composting can be used for the preparation of a dissolved organic carbon (DOC) solution. In this study, we used the DOC solutions for the remediation of a Zn-contaminated soil (with Zn concentrations up to 992 and 757 mg kg(-1) in topsoil and subsoil, respectively). We then determined the factors that affect Zn removal, such as pH, initial concentration of DOC solution, and washing frequency. Measurements using a Fourier Transform infrared spectrometer (FT-IR) revealed that carboxyl and amide were the major functional groups in the DOC solution obtained from the liquid fertilizer. Two soil washes using 1,500 mg L(-1) DOC solution with a of pH 2.0 at 25°C removed about 43% and 21% of the initial Zn from the topsoil and subsoil, respectively. Following this treatment, the pH of the soil declined from 5.4 to 4.1; organic matter content slightly increased from 6.2 to 6.5%; available ammonium (NH4(+)-N) content increased to 2.4 times the original level; and in the topsoil, the available phosphorus content and the exchangeable potassium content increased by 1.65 and 2.53 times their initial levels, respectively. Copyright © 2015 Elsevier B.V. All rights reserved.

Enhanced coagulation with powdered activated carbon or MIEX secondary treatment: a comparison of disinfection by-product formation and precursor removal.

PubMed

Watson, Kalinda; Farré, Maria José; Knight, Nicole

2015-01-01

The removal of both organic and inorganic disinfection by-product (DBP) precursors prior to disinfection is important in mitigating DBP formation, with halide removal being particularly important in salinity-impacted water sources. A matrix of waters of variable alkalinity, halide concentration and dissolved organic carbon (DOC) concentration were treated with enhanced coagulation (EC) followed by anion exchange (MIEX resin) or powdered activated carbon (PAC) and the subsequent disinfection by-product formation potentials (DBP-FPs) assessed and compared to DBP-FPs for untreated samples. Halide and DOC removal were also monitored for both treatment processes. Bromide and iodide adsorption by MIEX treatment ranged from 0 to 53% and 4-78%, respectively. As expected, EC and PAC treatments did not remove halides. DOC removal by EC/PAC was 70 ± 10%, while EC/MIEX enabled a DOC removal of 66 ± 12%. Despite the halide removals achieved by MIEX, increases in brominated disinfection by-product (Br-DBP) formation were observed relative to untreated samples, when favourable Br:DOC ratios were created by the treatment. However, the increases in formation were less than what was observed for the EC/PAC treated waters, which caused large increases in Br-DBP formation when high Br-DBP-forming water quality conditions occurred. The formation potential of fully chlorinated DBPs decreased after treatment in all cases.

Permafrost conditions in peatlands regulate magnitude, timing, and chemical composition of catchment dissolved organic carbon export.

PubMed

Olefeldt, David; Roulet, Nigel T

2014-10-01

Permafrost thaw in peatlands has the potential to alter catchment export of dissolved organic carbon (DOC) and thus influence downstream aquatic C cycling. Subarctic peatlands are often mosaics of different peatland types, where permafrost conditions regulate the hydrological setting of each type. We show that hydrological setting is key to observed differences in magnitude, timing, and chemical composition of DOC export between permafrost and nonpermafrost peatland types, and that these differences influence the export of DOC of larger catchments even when peatlands are minor catchment components. In many aspects, DOC export from a studied peatland permafrost plateau was similar to that of a forested upland catchment. Similarities included low annual export (2-3 g C m(-2) ) dominated by the snow melt period (~70%), and how substantial DOC export following storms required wet antecedent conditions. Conversely, nonpermafrost fens had higher DOC export (7 g C m(-2) ), resulting from sustained hydrological connectivity during summer. Chemical composition of catchment DOC export arose from the mixing of highly aromatic DOC from organic soils from permafrost plateau soil water and upland forest surface horizons with nonaromatic DOC from mineral soil groundwater, but was further modulated by fens. Increasing aromaticity from fen inflow to outlet was substantial and depended on both water residence time and water temperature. The role of fens as catchment biogeochemical hotspots was further emphasized by their capacity for sulfate retention. As a result of fen characteristics, a 4% fen cover in a mixed catchment was responsible for 34% higher DOC export, 50% higher DOC concentrations and ~10% higher DOC aromaticity at the catchment outlet during summer compared to a nonpeatland upland catchment. Expansion of fens due to thaw thus has potential to influence landscape C cycling by increasing fen capacity to act as biogeochemical hotspots, amplifying aquatic C cycling, and increasing catchment DOC export. © 2014 John Wiley & Sons Ltd.

Temporal changes in photoreactivity of dissolved organic carbon and implications for aquatic carbon fluxes from peatlands

NASA Astrophysics Data System (ADS)

Pickard, Amy E.; Heal, Kate V.; McLeod, Andrew R.; Dinsmore, Kerry J.

2017-04-01

Aquatic systems draining peatland catchments receive a high loading of dissolved organic carbon (DOC) from the surrounding terrestrial environment. Whilst photo-processing is known to be an important process in the transformation of aquatic DOC, the drivers of temporal variability in this pathway are less well understood. In this study, 8 h laboratory irradiation experiments were conducted on water samples collected from two contrasting peatland aquatic systems in Scotland: a peatland stream and a reservoir in a catchment with high percentage peat cover. Samples were collected monthly at both sites from May 2014 to May 2015 and from the stream system during two rainfall events. DOC concentrations, absorbance properties and fluorescence characteristics were measured to investigate characteristics of the photochemically labile fraction of DOC. CO2 and CO produced by irradiation were also measured to determine gaseous photoproduction and intrinsic sample photoreactivity. Significant variation was seen in the photoreactivity of DOC between the two systems, with total irradiation-induced changes typically 2 orders of magnitude greater at the high-DOC stream site. This is attributed to longer water residence times in the reservoir rendering a higher proportion of the DOC recalcitrant to photo-processing. During the experimental irradiation, 7 % of DOC in the stream water samples was photochemically reactive and direct conversion to CO2 accounted for 46 % of the measured DOC loss. Rainfall events were identified as important in replenishing photoreactive material in the stream, with lignin phenol data indicating mobilisation of fresh DOC derived from woody vegetation in the upper catchment. This study shows that peatland catchments produce significant volumes of aromatic DOC and that photoreactivity of this DOC is greatest in headwater streams; however, an improved understanding of water residence times and DOC input-output along the source to sea aquatic pathway is required to determine the fate of peatland carbon.

The effects of salinity, pH, and dissolved organic matter on acute copper toxicity to the rotifer, Brachionus plicatilis ("L" strain).

PubMed

Arnold, W R; Diamond, R L; Smith, D S

2010-08-01

This paper presents data from original research for use in the development of a marine biotic ligand model and, ultimately, copper criteria for the protection of estuarine and marine organisms and their uses. Ten 48-h static acute (unfed) copper toxicity tests using the euryhaline rotifer Brachionus plicatilis ("L" strain) were performed to assess the effects of salinity, pH, and dissolved organic matter (measured as dissolved organic carbon; DOC) on median lethal dissolved copper concentrations (LC50). Reconstituted and natural saltwater samples were tested at seven salinities (6, 11, 13, 15, 20, 24, and 29 g/L), over a pH range of 6.8-8.6 and a range of dissolved organic carbon of <0.5-4.1 mg C/L. Water chemistry analyses (alkalinity, calcium, chloride, DOC, hardness, magnesium, potassium, sodium, salinity, and temperature) are presented for input parameters to the biotic ligand model. In stepwise multiple regression analysis of experimental results where salinity, pH, and DOC concentrations varied, copper toxicity was significantly related only to the dissolved organic matter content (pH and salinity not statistically retained; alpha=0.05). The relationship of the 48-h dissolved copper LC50 values and dissolved organic carbon concentrations was LC50 (microg Cu/L)=27.1xDOC (mg C/L)1.25; r2=0.94.

Does the combination of biochar and clinoptilolite enhance nutrient recovery from the liquid fraction of biogas digestate?

PubMed

Kocatürk-Schumacher, Nazlı Pelin; Zwart, Kor; Bruun, Sander; Brussaard, Lijbert; Jensen, Lars Stoumann

2017-05-01

Concentrating nutrients on biochar and clinoptilolite and subsequently using the nutrient-enriched sorbents as a fertiliser could be an alternative way to manage nutrients in digestate. In this study, we investigated the use of biochar and clinoptilolite columns in removing ammonium, potassium, orthophosphate and dissolved organic carbon (DOC) from the liquid fraction of digestate. Our objectives were to investigate the effect of the initial loading ratio between liquid and biochar on nutrient removal, and to investigate the effect of combining biochar with clinoptilolite on nutrient and DOC removal efficiency. Increasing the initial loading ratios increased nutrient concentrations on biochar to 8.61 mg NH 4 -N g -1 , 1.95 mg PO 4 -P g -1 and 13.01 mg DOC g -1 , but resulted in decreasing removal efficiencies. The combination of biochar and clinoptilolite resulted in improved ammonium, potassium and DOC removal efficiencies compared to biochar alone, but did not significantly change PO 4 -P removal efficiencies. Removal efficiencies with combined sorbents were up to 67% for ammonium, 58% for DOC and 58% for potassium. Clinoptilolite showed higher removal efficiencies compared to biochar alone, and combining clinoptilolite with biochar improved only total P removal efficiency. Concentrating nutrients with clinoptilolite and biochar may be an option when both sorbents are available at low cost.

Impact of water chemistry on the particle-specific toxicity of copper nanoparticles to Daphnia magna.

PubMed

Xiao, Yinlong; Peijnenburg, Willie J G M; Chen, Guangchao; Vijver, Martina G

2018-01-01

Toxicity of metallic nanoparticle suspensions (NP (total) ) is generally assumed to result from the combined effect of the particles present in suspensions (NP (particle) ) and their released ions (NP (ion) ). Evaluation and consideration of how water chemistry affects the particle-specific toxicity of NP (total) are critical for environmental risk assessment of nanoparticles. In this study, it was found that the toxicity of Cu NP (particle) to Daphnia magna, in line with the trends in toxicity for Cu NP (ion) , decreased with increasing pH and with increasing concentrations of divalent cations and dissolved organic carbon (DOC). Without the addition of DOC, the toxicity of Cu NP (total) to D. magna at the LC50 was driven mainly by Cu NP (ion) (accounting for ≥53% of the observed toxicity). However, toxicity of Cu NP (total) in the presence of DOC at a concentration ranging from 5 to 50mg C/L largely resulted from the NP (particle) (57%-85%), which could be attributable to the large reduction of the concentration of Cu NP (ion) and the enhancement of the stability of Cu NP (particle) when DOC was added. Our results indicate that water chemistry needs to be explicitly taken into consideration when evaluating the role of NP (particle) and NP (ion) in the observed toxicity of NP (total) . Copyright © 2017 Elsevier B.V. All rights reserved.

Radiocarbon and stable-isotope geochemistry of organic and inorganic carbon in Lake Superior

NASA Astrophysics Data System (ADS)

Zigah, Prosper K.; Minor, Elizabeth C.; Werne, Josef P.

2012-03-01

We present a lake-wide investigation of Lake Superior carbon and organic matter biogeochemistry using radiocarbon, stable isotope, and carbon concentrations. Dissolved inorganic carbon (DIC) abundance in the lake was 121-122 Tg C, with offshore concentration andδ13C values being laterally homogenous and tightly coupled to the physical and thermal regime and biochemical processes. Offshore Δ14C of DIC (50-65‰) exhibited lateral homogeneity and was more 14C enriched than co-occurring atmospheric CO2 (˜38‰); nearshore Δ14C of DIC (36-38‰) was similar to atmospheric CO2. Dissolved organic carbon (DOC) abundance was 14.2-16.4 Tg C. DOC's concentration and δ13C were homogenous in June (mixed lake), but varied laterally during August (stratification) possibly due to spatial differences in lake productivity. Throughout sampling, DOC had modern radiocarbon values (14-58‰) indicating a semilabile nature with a turnover time of ≤60 years. Lake particulate organic carbon (POC, 0.9-1.3 Tg C) was consistently 13C depleted relative to DOC. The δ15N of epilimnetic particulate organic nitrogen shifted to more negative values during stratification possibly indicating greater use of nitrate (rather than ammonium) by phytoplankton in August. POC's radiocarbon was spatially heterogeneous (Δ14C range: 58‰ to -303‰), and generally 14C depleted relative to DOC and DIC. POC 14C depletion could not be accounted for by black carbon in the lake but, because of its spatial and temporal distribution, is attributed to sediment resuspension. The presence of old POC within the epilimnion of the open lake indicates possible benthic-pelagic coupling in the lake's organic carbon cycle; the ultimate fate of this old POC bears further investigation.

Particulate organic matter quality influences nitrate retention and denitrification in stream sediments: evidence from a carbon burial experiment

USGS Publications Warehouse

Stelzer, Robert S.; Scott, J. Thad; Bartsch, Lynn; Parr, Thomas B.

2014-01-01

Organic carbon supply is linked to nitrogen transformation in ecosystems. However, the role of organic carbon quality in nitrogen processing is not as well understood. We determined how the quality of particulate organic carbon (POC) influenced nitrogen transformation in stream sediments by burying identical quantities of varying quality POC (northern red oak (Quercus rubra) leaves, red maple (Acer rubrum) leaves, red maple wood) in stream mesocosms and measuring the effects on nitrogen retention and denitrification compared to a control of combusted sand. We also determined how POC quality affected the quantity and quality of dissolved organic carbon (DOC) and dissolved oxygen concentration in groundwater. Nitrate and total dissolved nitrogen (TDN) retention were assessed by comparing solute concentrations and fluxes along groundwater flow paths in the mesocosms. Denitrification was measured by in situ changes in N2 concentrations (using MIMS) and by acetylene block incubations. POC quality was measured by C:N and lignin:N ratios and DOC quality was assessed by fluorescence excitation emission matrix spectroscopy. POC quality had strong effects on nitrogen processing. Leaf treatments had much higher nitrate retention, TDN retention and denitrification rates than the wood and control treatments and red maple leaf burial resulted in higher nitrate and TDN retention rates than burial of red oak leaves. Leaf, but not wood, burial drove pore water to severe hypoxia and leaf treatments had higher DOC production and different DOC chemical composition than the wood and control treatments. We think that POC quality affected nitrogen processing in the sediments by influencing the quantity and quality of DOC and redox conditions. Our results suggest that the type of organic carbon inputs can affect the rates of nitrogen transformation in stream ecosystems.

Biochar feedstock and pyrolysis temperature effects on leachate: DOC characteristics and nitrate losses from a Brazilian Cerrado Arenosol mixed with agricultural waste biochars.

PubMed

Speratti, Alicia B; Johnson, Mark S; Sousa, Heiriane Martins; Dalmagro, Higo J; Couto, Eduardo Guimarães

2018-04-01

Dissolved organic carbon (DOC) leached from Brazilian Cerrado Arenosols can lead to carbon (C) losses and lower soil fertility, while excessive nutrient, e.g. nitrate (NO 3 - ), leaching can potentially cause water contamination. As biochar has been shown to stabilize C and retain soil nutrients, a greenhouse experiment was conducted to test different biochars' contributions to DOC and NO 3 - leaching from a sandy soil. Biochars were made from four local agricultural waste feedstocks (cotton residue, swine manure, eucalyptus sawmill residue, sugarcane filtercake) pyrolysed at 400, 500 and 600 °C. Biochar was mixed with soil at 5% weight in pots and maize seeds planted. Leachate was collected weekly for six weeks and analyzed for DOC and NO 3 - concentrations, while fluorescence spectroscopy with parallel factor analysis (PARAFAC) was used to interpret DOC characteristics. Cotton and swine manure biochar treatments had higher DOC and NO 3 - losses than eucalyptus biochar, filtercake biochar, and control treatments. Cotton and swine manure biochar treatments at high temperatures lost mostly terrestrial, humified DOC, while swine manure, filtercake, and eucalyptus biochars at low temperatures lost mostly labile, microbially-derived DOC. Through the practical use of fluorescence spectroscopy, our study identified filtercake and eucalyptus biochars as most promising for retaining DOC and NO 3 - in a Cerrado Arenosol, potentially reducing stable C and nutrient losses. Copyright © 2018 Elsevier Ltd. All rights reserved.

Towards a universal microbial inoculum for dissolved organic carbon degradation experiments

NASA Astrophysics Data System (ADS)

Pastor, Ada; Catalán, Núria; Gutiérrez, Carmen; Nagar, Nupur; Casas-Ruiz, Joan P.; Obrador, Biel; von Schiller, Daniel; Sabater, Sergi; Petrovic, Mira; Borrego, Carles M.; Marcé, Rafael

2017-04-01

Dissolved organic carbon (DOC) is the largest biologically available pool of organic carbon in aquatic ecosystems and its degradation along the land-to-ocean continuum has implications for carbon cycling from local to global scales. DOC biodegradability is usually assessed by incubating filtered water inoculated with native microbial assemblages in the laboratory. However, the use of a native inoculum from several freshwaters, without having a microbial-tailored design, hampers our ability to tease apart the relative contribution of the factors driving DOC degradation from the effects of local microbial communities. The use of a standard microbial inoculum would allow researchers to disentangle the drivers of DOC degradation from the metabolic capabilities of microbial communities operating in situ. With this purpose, we designed a bacterial inoculum to be used in experiments of DOC degradation in freshwater habitats. The inoculum is composed of six bacterial strains that easily grow under laboratory conditions, possess a versatile metabolism and are able to grow under both aerobic and anaerobic conditions. The mixed inoculum showed higher DOC degradation rates than those from their isolated bacterial components and the consumption of organic substrates was consistently replicated. Moreover, DOC degradation rates obtained using the designed inoculum were responsive across a wide range of natural water types differing in DOC concentration and composition. Overall, our results show the potential of the designed inoculum as a tool to discriminate between the effects of environmental drivers and intrinsic properties of DOC on degradation dynamics.

Seasonal Dynamics of Soil Labile Organic Carbon and Enzyme Activities in Relation to Vegetation Types in Hangzhou Bay Tidal Flat Wetland

PubMed Central

Shao, Xuexin; Yang, Wenying; Wu, Ming

2015-01-01

Soil labile organic carbon and soil enzymes play important roles in the carbon cycle of coastal wetlands that have high organic carbon accumulation rates. Soils under three vegetations (Phragmites australis, Spartina alterniflora, and Scirpusm mariqueter) as well as bare mudflat in Hangzhou Bay wetland of China were collected seasonally. Seasonal dynamics and correlations of soil labile organic carbon fractions and soil enzyme activities were analyzed. The results showed that there were significant differences among vegetation types in the contents of soil organic carbon (SOC) and dissolved organic carbon (DOC), excepting for that of microbial biomass carbon (MBC). The P. australis soil was with the highest content of both SOC (7.86 g kg-1) and DOC (306 mg kg-1), while the S. mariqueter soil was with the lowest content of SOC (6.83 g kg-1), and the bare mudflat was with the lowest content of DOC (270 mg kg-1). Soil enzyme activities were significantly different among vegetation types except for urease. The P. australis had the highest annual average activity of alkaline phosphomonoesterase (21.4 mg kg-1 h-1), and the S. alterniflora had the highest annual average activities of β-glycosidase (4.10 mg kg-1 h-1) and invertase (9.81mg g-1 24h-1); however, the bare mudflat had the lowest activities of alkaline phosphomonoesterase (16.2 mg kg-1 h-1), β-glycosidase (2.87 mg kg-1 h-1), and invertase (8.02 mg g-1 24h-1). Analysis also showed that the soil labile organic carbon fractions and soil enzyme activities had distinct seasonal dynamics. In addition, the soil MBC content was significantly correlated with the activities of urease and β-glucosidase. The DOC content was significantly correlated with the activities of urease, alkaline phosphomonoesterase, and invertase. The results indicated that vegetation type is an important factor influencing the spatial-temporal variation of soil enzyme activities and labile organic carbon in coastal wetlands. PMID:26560310

Biodegradability of DBP precursors after drinking water ozonation.

PubMed

de Vera, Glen Andrew; Keller, Jurg; Gernjak, Wolfgang; Weinberg, Howard; Farré, Maria José

2016-12-01

Ozonation is known to generate biodegradable organic matter, which is typically reduced by biological filtration to avoid bacterial regrowth in distribution systems. Post-chlorination generates halogenated disinfection byproducts (DBPs) but little is known about the biodegradability of their precursors. This study determined the effect of ozonation and biofiltration conditions, specifically ozone exposure and empty bed contact time (EBCT), on the control of DBP formation potentials in drinking water. Ozone exposure was varied through addition of H 2 O 2 during ozonation at 1 mgO 3 /mgDOC followed by biological filtration using either activated carbon (BAC) or anthracite. Ozonation led to a 10% decrease in dissolved organic carbon (DOC), without further improvement from H 2 O 2 addition. Raising H 2 O 2 concentrations from 0 to 2 mmol/mmolO 3 resulted in increased DBP formation potentials during post-chlorination of the ozonated water (target Cl 2 residual after 24 h = 1-2 mg/L) as follows: 4 trihalomethanes (THM4, 37%), 8 haloacetic acids (HAA8, 44%), chloral hydrate (CH, 107%), 2 haloketones (HK2, 97%), 4 haloacetonitriles (HAN4, 33%), trichloroacetamide (TCAM, 43%), and adsorbable organic halogen (AOX, 27%), but a decrease in the concentrations of 2 trihalonitromethanes (THNM2, 43%). Coupling ozonation with biofiltration prior to chlorination effectively lowered the formation potentials of all DBPs including CH, HK2, and THNM2, all of which increased after ozonation. The dynamics of DBP formation potentials during BAC filtration at different EBCTs followed first-order reaction kinetics. Minimum steady-state concentrations were attained at an EBCT of about 10-20 min, depending on the DBP species. The rate of reduction in DBP formation potentials varied among individual species before reaching their minimum concentrations. CH, HK2, and THNM2 had the highest rate constants of between 0.5 and 0.6 min -1 followed by HAN4 (0.4 min -1 ), THM4 (0.3 min -1 ), HAA8 (0.2 min -1 ), and AOX (0.1 min -1 ). At an EBCT of 15 min, the reduction in formation potential for most DBPs was less than 50% but was higher than 70% for CH, HK2, and THNM2. The formation of bromine-containing DBPs increased with increasing EBCT, most likely due to an increase in Br - /DOC ratio. Overall, this study demonstrated that the combination of ozonation and biofiltration is an effective approach to mitigate DBP formation during drinking water treatment. Copyright © 2016 Elsevier Ltd. All rights reserved.

Production of glycolic acid by chemolithotrophic iron- and sulfur-oxidizing bacteria and its role in delineating and sustaining acidophilic sulfide mineral-oxidizing consortia.

PubMed

Nancucheo, Ivan; Johnson, D Barrie

2010-01-01

Glycolic acid was detected as an exudate in actively growing cultures of three chemolithotrophic acidophiles that are important in biomining operations, Leptospirillum ferriphilum, Acidithiobacillus (At.) ferrooxidans, and At. caldus. Although similar concentrations of glycolic acid were found in all cases, the concentrations corresponded to ca. 24% of the total dissolved organic carbon (DOC) in cultures of L. ferriphilum but only ca. 5% of the total DOC in cultures of the two Acidithiobacillus spp. Rapid acidification (to pH 1.0) of the culture medium of At. caldus resulted in a large increase in the level of DOC, although the concentration of glycolic acid did not change in proportion. The archaeon Ferroplasma acidiphilum grew in the cell-free spent medium of At. caldus; glycolic acid was not metabolized, although other unidentified compounds in the DOC pool were metabolized. Glycolic acid exhibited levels of toxicity with 21 strains of acidophiles screened similar to those of acetic acid. The most sensitive species were chemolithotrophs (L. ferriphilum and At. ferrivorans), while the most tolerant species were chemoorganotrophs (Acidocella, Acidobacterium, and Ferroplasma species), and the ability to metabolize glycolic acid appeared to be restricted (among acidophiles) to Firmicutes (chiefly Sulfobacillus spp.). Results of this study help explain why Sulfobacillus spp. rather than other acidophiles are the main organic carbon-degrading bacteria in continuously fed stirred tanks used to bioprocess sulfide mineral concentrates and also why temporary cessation of pH control in these systems, resulting in rapid acidification, often results in a plume of the archaeon Ferroplasma.

The biogeochemistry of carbon across a gradient of streams and rivers within the Congo Basin

NASA Astrophysics Data System (ADS)

Mann, P. J.; Spencer, R. G. M.; Dinga, B. J.; Poulsen, J. R.; Hernes, P. J.; Fiske, G.; Salter, M. E.; Wang, Z. A.; Hoering, K. A.; Six, J.; Holmes, R. M.

2014-04-01

Dissolved organic carbon (DOC) and inorganic carbon (DIC, pCO2), lignin biomarkers, and theoptical properties of dissolved organic matter (DOM) were measured in a gradient of streams and rivers within the Congo Basin, with the aim of examining how vegetation cover and hydrology influences the composition and concentration of fluvial carbon (C). Three sampling campaigns (February 2010, November 2010, and August 2011) spanning 56 sites are compared by subbasin watershed land cover type (savannah, tropical forest, and swamp) and hydrologic regime (high, intermediate, and low). Land cover properties predominately controlled the amount and quality of DOC, chromophoric DOM (CDOM) and lignin phenol concentrations (∑8) exported in streams and rivers throughout the Congo Basin. Higher DIC concentrations and changing DOM composition (lower molecular weight, less aromatic C) during periods of low hydrologic flow indicated shifting rapid overland supply pathways in wet conditions to deeper groundwater inputs during drier periods. Lower DOC concentrations in forest and swamp subbasins were apparent with increasing catchment area, indicating enhanced DOC loss with extended water residence time. Surface water pCO2 in savannah and tropical forest catchments ranged between 2,600 and 11,922 µatm, with swamp regions exhibiting extremely high pCO2 (10,598-15,802 µatm), highlighting their potential as significant pathways for water-air efflux. Our data suggest that the quantity and quality of DOM exported to streams and rivers are largely driven by terrestrial ecosystem structure and that anthropogenic land use or climate change may impact fluvial C composition and reactivity, with ramifications for regional C budgets and future climate scenarios.

Mercury cycling in stream ecosystems. 1. Water column chemistry and transport

USGS Publications Warehouse

Brigham, M.E.; Wentz, D.A.; Aiken, G.R.; Krabbenhoft, D.P.

2009-01-01

We studied total mercury (THg) and methylmercury (MeHg) in eight streams, located in Oregon, Wisconsin, and Florida, that span large ranges in climate, landscape characteristics, atmospheric Hg deposition, and water chemistry. While atmospheric deposition was the source of Hg at each site, basin characteristics appeared to mediate this source by providing controls on methylation and fluvial THg and MeHg transport. Instantaneous concentrations of filtered total mercury (FTHg) and filtered methylmercury (FMeHg) exhibited strong positive correlations with both dissolved organic carbon (DOC) concentrations and streamflow for most streams, whereas mean FTHg and FMeHg concentrations were correlated with wetland density of the basins. For all streams combined, whole water concentrations (sum of filtered and particulate forms) of THg and MeHg correlated strongly with DOC and suspended sediment concentrations in the water column. ?? 2009 American Chemical Society.

Effects of Coral Reef Benthic Primary Producers on Dissolved Organic Carbon and Microbial Activity

PubMed Central

Haas, Andreas F.; Nelson, Craig E.; Wegley Kelly, Linda; Carlson, Craig A.; Rohwer, Forest; Leichter, James J.; Wyatt, Alex; Smith, Jennifer E.

2011-01-01

Benthic primary producers in marine ecosystems may significantly alter biogeochemical cycling and microbial processes in their surrounding environment. To examine these interactions, we studied dissolved organic matter release by dominant benthic taxa and subsequent microbial remineralization in the lagoonal reefs of Moorea, French Polynesia. Rates of photosynthesis, respiration, and dissolved organic carbon (DOC) release were assessed for several common benthic reef organisms from the backreef habitat. We assessed microbial community response to dissolved exudates of each benthic producer by measuring bacterioplankton growth, respiration, and DOC drawdown in two-day dark dilution culture incubations. Experiments were conducted for six benthic producers: three species of macroalgae (each representing a different algal phylum: Turbinaria ornata – Ochrophyta; Amansia rhodantha – Rhodophyta; Halimeda opuntia – Chlorophyta), a mixed assemblage of turf algae, a species of crustose coralline algae (Hydrolithon reinboldii) and a dominant hermatypic coral (Porites lobata). Our results show that all five types of algae, but not the coral, exuded significant amounts of labile DOC into their surrounding environment. In general, primary producers with the highest rates of photosynthesis released the most DOC and yielded the greatest bacterioplankton growth; turf algae produced nearly twice as much DOC per unit surface area than the other benthic producers (14.0±2.8 µmol h−1 dm−2), stimulating rapid bacterioplankton growth (0.044±0.002 log10 cells h−1) and concomitant oxygen drawdown (0.16±0.05 µmol L−1 h−1 dm−2). Our results demonstrate that benthic reef algae can release a significant fraction of their photosynthetically-fixed carbon as DOC, these release rates vary by species, and this DOC is available to and consumed by reef associated microbes. These data provide compelling evidence that benthic primary producers differentially influence reef microbial dynamics and biogeochemical parameters (i.e., DOC and oxygen availability, bacterial abundance and metabolism) in coral reef communities. PMID:22125645

Examination of mercury and organic carbon dynamics from a constructed fen in the Athabasca oil sands region, Alberta, Canada using in situ and laboratory fluorescence measurements

NASA Astrophysics Data System (ADS)

Oswald, C.; Carey, S. K.

2013-12-01

In the Athabasca oil sands region, mined landscapes must be reclaimed to a functioning natural ecosystem as part of the mine closure process. To test wetland construction techniques on oil sands tailings, 55 ha of mined landscape on the Syncrude Canada Ltd. property is being reclaimed to a watershed containing a graminoid fen. The 18 ha constructed fen consists of an approximately 50 cm thick peat-mineral soil layer separated from underlying tailings sand by a thin layer of clay till. The water table in the fen is maintained by pumping water into the fen from a nearby lake and controlling outflow with under-drains. The objective of this study was to assess total mercury (THg) and methyl mercury (MeHg) concentration dynamics in water exported from the fen in relation to organic carbon quantity and composition. Water quality data from summer 2012 when the fen pumps were first turned on show that dissolved organic carbon (DOC) concentrations are on average twice as high in water flowing through the underlying tailings sand aquifer (median: 42.0 mg/L) compared to DOC concentrations in water flowing through the fen peat package (median: 20.3 mg/L). Given these DOC concentrations, filtered THg concentrations are very low (median values are 0.81 ng/L and 0.17 ng/L for water flowing through the fen peat and sand tailings, respectively) compared to concentrations reported for other boreal wetlands. Although a relationship was identified between filtered THg and DOC (r2=0.60), its slope (0.06 ng Hg/mg C) is an order-of-magnitude smaller than the typical range of slopes found at other wetland sites potentially suggesting a small pool of mercury in the peat and/or limited partitioning of mercury into solution. Filtered MeHg concentrations in all water samples are near the limit of detection and suggest that biogeochemical conditions conducive to methylation did not exist in the fen peat or tailings sand at the time of sampling. In addition to these baseline THg and MeHg results that will be used to assess the evolution of mercury dynamics in the fen as the hydrology and vegetation become established, we are investigating the composition of dissolved organic matter (DOM) using optical techniques in the water flowing through the fen peat and underlying tailing sand aquifer. During 2013, continuous in situ measurements of chromophoric DOM fluorescence (FDOM) were measured at the fen outlet to identify sources of C and their relative contribution to discharge waters. We compare these field measurements to laboratory measurements of FDOM on discrete water samples using a benchtop spectrofluorometer to develop relationships between FDOM, DOC and filtered THg and MeHg. The use of continuous in situ FDOM measurements as a proxy for DOC and mercury concentrations will improve our understanding of the effects of hydrologic management and natural seasonal variations in fen hydrology on DOC and Hg fluxes from different soil layers in the constructed system. Furthermore, we expect that the modeling of excitation-emission matrices using parallel factor analysis on discrete water samples will provide important information on the sources and reactivity of organic carbon being transported through different soil compartments in the fen.

Role of Ca-bentonite to improve the humification, enzymatic activities, nutrient transformation and end product quality during sewage sludge composting.

PubMed

Awasthi, Mukesh Kumar; Awasthi, Sanjeev Kumar; Wang, Quan; Awasthi, Mrigendra Kumar; Zhao, Junchao; Chen, Hongyu; Ren, Xiuna; Wang, Meijing; Zhang, Zengqiang

2018-04-10

This study was aimed to examine the response of Ca-bentonite (CB) amendment to improve the sewage sludge (SS) composting along with wheat straw (WS) as bulking agent. Five treatments (SS + WS) were mixed with or without blending of discrepant concentration of CB (2%, 4%, 6%, and 10%), respectively, and without CB added treatment applied as the control. The results showed that compared to control and 2%CB blended treatments, while the 6-10%CB -amended treatment indicated maximum enzymatic activities with the composting progress and highest organic matter degradation and loss. The amendment of 6-10%CB increased the humic acid, HA/FA ratio, DON, NH 4 + -N, NO 3 and DOC but reduced the fulvic acids content and the maturity period by 2 weeks as compared to control. In addition, maturity parameters also confirmed that the highest seed germination was observed with the 10%CB applied compost followed by 6%CB, 4%CB and 2%CB applied treatments, respectively. Copyright © 2018 Elsevier Ltd. All rights reserved.

DOC export from a peat extraction site in transition to managed restoration - preliminary results of a long-term research project

NASA Astrophysics Data System (ADS)

Rüggen, Norman; Kutzbach, Lars; Kopelke, Susanne; Pfeiffer, Eva-Maria

2013-04-01

Peatlands play a major role in the global cycles of water and carbon. Budgeting carbon fluxes of temperate man-managed peatlands is limited by few available data. The main carbon compounds exported from such sites are CO2, CH4 and laterally exported C compounds (dissolved organic carbon (DOC) and gases). Without reliable estimates of laterally exported carbon from managed peatlands, overall carbon balances of such geoecosystems remain obscure. The Himmelmoor peatland in Schleswig-Holstein is subject to horticultural peat extraction in transition towards managed restoration. One-third of 130 ha of peatland area are already subject to managed restoration, the remaining part is still intensively used as a peat extraction site. Surface water discharge rates are measured by a water head sensor in combination with a rectangular-shaped weir. An October-November data set (54 days period, 2012) shows a distinct base-flow and precipitation-dependent discharge peaks, which were up to five times higher than the base-flow. The observations indicate a poor water storing capacity of the intensively used areas. During this first observation period, almost 65,000 tons of peatland-DOC-bearing water have been discharged into the adjacent river system. DOC concentrations in the discharge water have been measured every 6-12 days with a Total Carbon Analyzer TOC-L (Shimadzu, Japan). Additionally, a field spectrophotometer (spectro::lyser,s-can, Austria) has been employed, for measuring quasi-continuous concentrations of DOC. During the 54 day period, approximately 1.75 g DOC m-2 (or about 1750 kg DOC km-2) has been laterally exported from the peatland. Average DOC concentration was 35.1 ± 4 g l-1. These values range in the same order of magnitude that have been published from managed UK peatlands (Armstrong et al., 2010; Wilson et al., 2011). Preliminary data evaluation of the in-situ field spectrophotometer show that DOC concentrations of discharge water varied up to 1.5 mg L-1 in less than six hours and up to about 3 mg L-1 in 36 hours. The described recently established hydrological measurements are planned to be continued for the next ten years in combination with continuous eddy covariance measurements of land-atmosphere fluxes of Water, CO2 and CH4. This long-term monitoring of lateral and vertical exchange fluxes will serve as a basis for evaluating the success of the peatland restoration with respect to biogeochemical cycling and greenhouse gas budgets. Literature Armstrong, A., Holden, J., Kay, P., Francis, B., Foulger, M., Gledhill, S., McDonald, A., Walker, A., 2010. The impact of peatland drain-blocking on dissolved organic carbon loss and discolouration of water; results from a national survey. Journal of Hydrology 381, 112-120. Wilson, L., Wilson, J., Holden, J., Johnstone, I., Armstrong, A., Morris, M., 2011. Ditch blocking, water chemistry and organic carbon flux: Evidence that blanket bog restoration reduces erosion and fluvial carbon loss. Science of the Total Environment 409, 2010-2018.

The impact of adding organic carbon on the concentrations of total residual oxidants and disinfection by-products in approval tests for ballast water management systems.

PubMed

Lee, Jihyun; Shon, Myung-Baek; Cha, Hyung-Gon; Choi, Keun-Hyung

2017-12-15

In the G8 and G9 approval tests for ballast water management systems, organic carbon additives are frequently supplemented into test water to satisfy the water quality requirements. Because organic additives can affect the approval test, the additive selected, and its use and validation should be included in the test report. This study assessed the effects of organic carbon additives on the concentration of total residual oxidants (TROs) and the formation of disinfection by-products (DBPs). The concentration of dissolved organic carbon (DOC) in test water containing additives varied depending on the type of additive, but all additives, except for methylcellulose, had concentrations similar to or higher than the theoretical values. There was a low concentration of particulate organic carbon (POC) compared to the amount of corn starch added. Over the course of the five-day holding time, TRO concentrations tended to decrease. In general, substances with a large molecular size had a higher DBP concentration than their counterparts with a smaller molecular size, some of which, however produced the highest DBP concentrations due to their molecular structure. The results suggest that the formation of DBPs is affected by the reaction with TROs, molecular size, and molecular structure in a complex manner. Copyright © 2017 Elsevier B.V. All rights reserved.

Estimating the Concentration and Biodegradability of Organic Matter in 22 Wastewater Treatment Plants Using Fluorescence Excitation Emission Matrices and Parallel Factor Analysis

PubMed Central

Yang, Liyang; Shin, Hyun-Sang; Hur, Jin

2014-01-01

This study aimed at monitoring the changes of fluorescent components in wastewater samples from 22 Korean biological wastewater treatment plants and exploring their prediction capabilities for total organic carbon (TOC), dissolved organic carbon (DOC), biochemical oxygen demand (BOD), chemical oxygen demand (COD), and the biodegradability of the wastewater using an optical sensing technique based on fluorescence excitation emission matrices and parallel factor analysis (EEM-PARAFAC). Three fluorescent components were identified from the samples by using EEM-PARAFAC, including protein-like (C1), fulvic-like (C2) and humic-like (C3) components. C1 showed the highest removal efficiencies for all the treatment types investigated here (69% ± 26%–81% ± 8%), followed by C2 (37% ± 27%–65% ± 35%), while humic-like component (i.e., C3) tended to be accumulated during the biological treatment processes. The percentage of C1 in total fluorescence (%C1) decreased from 54% ± 8% in the influents to 28% ± 8% in the effluents, while those of C2 and C3 (%C2 and %C3) increased from 43% ± 6% to 62% ± 9% and from 3% ± 7% to 10% ± 8%, respectively. The concentrations of TOC, DOC, BOD, and COD were the most correlated with the fluorescence intensity (Fmax) of C1 (r = 0.790–0.817), as compared with the other two fluorescent components. The prediction capability of C1 for TOC, BOD, and COD were improved by using multiple regression based on Fmax of C1 and suspended solids (SS) (r = 0.856–0.865), both of which can be easily monitored in situ. The biodegradability of organic matter in BOD/COD were significantly correlated with each PARAFAC component and their combinations (r = −0.598–0.613, p < 0.001), with the highest correlation coefficient shown for %C1. The estimation capability was further enhanced by using multiple regressions based on %C1, %C2 and C3/C2 (r = −0.691). PMID:24448170

Mercury and Organic Carbon Relationships in Streams Draining Forested Upland/Peatland Watersheds

Treesearch

R. K. Kolka; D. F. Grigal; E. S. Verry; E. A. Nater

1999-01-01

We determined the fluxes of total mecury (HgT), total organic carbon (TOC), and dissolved organic carbon (DOC) from five upland/peatland watersheds at the watershed outlet. The difference between TOC and DOC was defined as particulate OC (POC). Concentrations of HgT showed moderate to strong relationships with POC (R2 = 0.77) when all watersheds...

Mercury and Organic Carbon Relationships in Streams Draining Forested Upland/Peatland Watersheds

Treesearch

Randall K. Kolka; D.F. Grigal; E.S. Verry; E.A. Nater

1999-01-01

We determined the fluxes of total mercury (HgT), total organic carbon (TOC), and dissolved organic carbon (DOC) from five upland/peatland watersheds at the watershed outlet. The difference between TOC and DOC was defined as particulate OC (POC). Concentrations of HgT showed moderate to strong relationships with POC (R2 = 0.77) when ah...

Flushing of distal hillslopes as an alternative source of stream dissolved organic carbon in a headwater catchment

Treesearch

John P. Gannon; Scott W. Bailey; Kevin J. McGuire; James B. Shanley

2015-01-01

We investigated potential source areas of dissolved organic carbon (DOC) in headwater streams by examining DOC concentrations in lysimeter, shallow well, and stream water samples from a reference catchment at the Hubbard Brook Experimental Forest. These observations were then compared to high-frequency temporal variations in fluorescent dissolved organic matter (FDOM)...

Bioavailability of Dissolved Organic Carbon and Nitrogen From Tropical Montane Rainforest Streams Across a Geologic age Gradient

NASA Astrophysics Data System (ADS)

Wiegner, T. N.

2005-05-01

Dissolved organic matter (DOM) is metabolically important in streams. Its bioavailability is influenced by organic matter sources to streams and inorganic nutrient availability. As forest canopies and soils develop over time, organic matter inputs to streams should switch from algal to watershed sources. Across this succession gradient, nutrient limitation should also change. This study examines how chemical composition and bioavailability of DOM from tropical montane rainforest streams on Hawaii change across a geologic age gradient from 4 ky to 150 ky. Dissolved organic C (DOC) and N (DON) concentrations, chemical characteristics, and bioavailability varied with site age. With increasing stream age, DOC and DON concentrations, DOM aromaticity, and the C:N of the stream DOM increased. Changes in stream DOM chemistry and inorganic nutrient availability affected DOM bioavailability. Fifty percent of the DOC from the 4 ky site was bioavailable, where little to none was bioavailable from the older streams. Inorganic nutrient availability did not affect DOC bioavailability. In contrast, DON bioavailability was similar (12%) across sites and was affected by inorganic nutrient availability. This study demonstrates that the chemistry and metabolism of streams draining forests change with ecosystem age and development.

Using polyacrylate-coated SPME fibers to quantify sorption of polar and ionic organic contaminants to dissolved organic carbon.

PubMed

Haftka, Joris J-H; Scherpenisse, Peter; Jonker, Michiel T O; Hermens, Joop L M

2013-05-07

A passive sampling method using polyacrylate-coated solid-phase microextraction (SPME) fibers was applied to determine sorption of polar and ionic organic contaminants to dissolved organic carbon (DOC). The tested contaminants included pharmaceuticals, industrial chemicals, hormones, and pesticides and represented neutral, anionic, and cationic structures. Prior to the passive sampler application, sorption of the chemicals to the fibers was characterized. This was needed in order to accurately translate concentrations measured in fibers to freely dissolved aqueous concentrations during the sorption tests with DOC. Sorption isotherms of neutral compounds to the fiber were linear, whereas isotherms of basic chemicals covered a nonlinear and a linear range. Sorption of acidic and basic compounds to the fiber was pH-dependent and was dominated by sorption of the neutral sorbate species. Fiber- and DOC-water partition coefficients of neutral compounds were both linearly related to octanol-water partition coefficients (log Kow). The results of this study show that polyacrylate fibers can be used to quantify sorption to DOC of neutral and ionic contaminants, having multiple functional groups and spanning a wide hydrophobicity range (log Kow = 2.5-7.5).