Modeling the carbon dynamics of the La Grande hydroelectric complex in northern Quebec

A mechanistic semi-empirical carbon cycle model of the La Grande reservoir complex in northern Quebec, Canada was conceived in order to investigate the climate impact of such a large alteration of the continental water cycle. The model includes inputs from the drainage basin, organic matter release from flooded soils, CO₂ emissions across the water-atmosphere interface and sedimentation. Most input data stems from previous research by our group on those ecosystems. The model includes the seven reservoirs of the La Grande complex and was run for periods of 50 and 100 years. Terrigeneous dissolved, particulate and suspended soil carbon fluxes and concentrations were computed. Over 100 years, 31.3 × 10¹² g C are released from flooded soils, equivalent to 28-29% of inputs from the drainage basin. 40-74% of dissolved organic carbon is mineralized. CO₂ fluxes over 100 years are 50.5-79.8 × 10¹² g C, 46.4-67.9 × 10¹² g C more than in the absence of reservoirs. The increase in mineralization of organic matter and in CO₂ emissions is a result of the increase in cumulated water residence time due to the creation of the reservoirs. Changes in other carbon sinks and sources likely offset a part of this additional carbon flux to the atmosphere. In the first years following flooding of the reservoir, organic carbon release from flooded soils exceeds CO₂ emissions, implying the downstream export of large quantities of eroded soil organic carbon. After this initial period, CO₂ emissions are fuelled by organic carbon originating from the drainage basin.     

Distribution,fate and formation of non-extractable residues of a nonylphenol isomer in soil with special emphasis on soil derived organo-clay complexes

Anthropogenic contaminants like nonylphenols (NP) are added to soil, for instance if sewage-sludge is used as fertilizer in agriculture. A commercial mixture of NP consists of more than 20 isomers. For our study, we used one of the predominate isomers of NP mixtures, 4-(3,5-dimethylhept-3-yl)phenol, as a representative compound. The aim was to investigate the fate and distribution of the isomer within soil and soil derived organo-clay complexes. Therefore, ¹⁴C- and ¹³C-labeled NP was added to soil samples and incubated up to 180 days. Mineralization was measured and soil samples were fractionated into sand, silt and clay; the clay fraction was further separated in humic acids, fulvic acids and humin. The organo-clay complexes pre-incubated for 90 or 180 days were re-incubated with fresh soil for 180 days, to study the potential of re-mobilization of incorporated residues. The predominate incorporation sites of the nonylphenol isomer in soil were the organo-clay complexes. After 180 days of incubation, 22 % of the applied ¹⁴C was mineralized. The bioavailable, water extractable portion was low (9 % of applied ¹⁴C) and remained constant during the entire incubation period, which could be explained by an incorporation/release equilibrium. Separation of organo-clay complexes, after extraction with solvents to release weakly incorporated, bioaccessible portions, showed that non-extractable residues (NER) were preferentially located in the humic acid fraction, which was regarded as an effect of the chemical composition of this fraction. Generally, 27 % of applied ¹⁴C was incorporated into organo-clay complexes as NER, whereas 9 % of applied ¹⁴C was bioaccessible after 180 days of incubation. The re-mobilization experiments showed on the one hand, a decrease of the bioavailability of the nonylphenol residues due to stronger incorporation, when the pre-incubation period was increased from 90 to 180 days. On the other hand, a shift of these residues from the clay fraction to other soil fractions was observed, implying a dynamic behavior of incorporated residues, which may result in bioaccessibility of the NER of nonylphenol.     

Ozone-driven photocatalyzed degradation and mineralization of pesticide,Triclopyr by Au/TiO2

Triclopyr is a widely used pesticide which is non-biodegradable and enters aquatic systems. The ozone facilitated photocatalyzed degradation and mineralization of Triclopyr using Au-loaded titania as heterogeneous catalyst is reported. The oxidative degradation activity of the hazardous pesticide was investigated at pH 7.8 under varied reaction conditions, including in presence and absence of ozone, titania alone, in presence and absence of light and with different loadings of Au on support. Photocatalysis with 2% Au/TiO₂ in the presence of ozone yielded 100% degradation of Triclopyr in 2 h. The extent of degradation of pesticide and its mineralization were confirmed by GC-MS. For 10 mg/L of Triclopyr, 0.1 g/L of catalyst was found to be the optimum for mineralization. Results show that photocatalyzed ozonation with Au/TiO₂ as catalyst is a very effective for its removal. No leaching of Au was observed in triplicate runs. Catalyst was fully recoverable and reusable with no loss of activity.     

CHEMISTRY RESPONSE OF TWO FORESTED WATERSHEDS TO ACID ATMOSPHERIC DEPOSITION1

ABSTRACT: The deposition and chemistry of precipitation were estimated for one year in two forest ecosystems in the South-Central United States. Precipitation, throughfall, litter leachate, and soil leachate were analyzed for a small catchment of pine-hardwoods in southeastern Oklahoma and for a catchment of loblolly pines (Pinus taeda L.) in northern Mississippi. In the pine-hardwood forest, 98 percent of the acid deposition was neutralized, 50 percent in the forest canopy, and 48 percent in the forest floor. In the pine forest, 75 percent of the acid deposition was neutralized, all in the forest floor. The pine-hardwood ecosystem accumulated sulfate, nitrate, and ammonia ions, and lost base cations. During seasons of deficient precipitation, dry deposition appeared to enrich the concentrations of hydrogen, nitrate, sulfate, and ammonia ions in throughfall samples at both locations.     

EFFECTS OF FOREST FERTILIZATION ON STREAM WATER CHEMISTRY IN THE APPALACHIANS1

ABSTRACT: Stream water chemistry was monitored on two watersheds on the Fernow Experimental Forest in north-central West Virginia to determine the effects of forest fertilization on annual nutrient exports. Ammonium nitrate and triple superphosphate were applied simultaneously at rates of 336 kg ha^?1 N and 224 kg ha^?1 P₂O₅, respectively, which are similar to rates used in commercial forest operations. The treatment significantly increased outputs of several ions. Annual outputs of nitrate N increased as much as 18 times over pretreatment levels, and calcium and magnesium increased as much as three times over pretreatment levels the first year after fertilization. Outputs for these nutrients were elevated for all three post-treatment years. Although nitrate N increased significantly, only about 20 percent of the applied fertilizer was accounted for in stream water exports. Outputs of phosphate P declined following fertilization, probably because the watersheds are phosphorus deficient, but by the third year, they slightly exceeded predicted values. Estimated nutrient losses to deep seepage were substantial, especially on the leakier south-facing catchmeat, on which some nutrient losses were equal to or greater than those in stream water. When the nutrient exports associated with both stream discharge and ground water recharge were combined, the percentages of applied N that were lost were similar on the two watersheds, averaging 27.5 percent. Less than 1 percent of the applied P was lost from either watershed in the combination of streamflow and deep seepage.     

OXIDIZED NITROGEN IN PRECIPITATION,THROUGHFALL, AND STREAMFALL FROM A FORESTED WATERSHED IN OKLAHOMA1

ABSTRACT: Oxidized nitrogen (nitrite + nitrate N) concentrations were measured from bulk precipitation, bulk through-fall, and streamflow in a 7.86 hectare forested watershed in southeastern Oklahoma during the wet season from March through June 1983. Oxidized nitrogen inputs comparable to results of other studies were recorded during the 19 rainstorms sampled. Oxidized nitrogen concentrations appeared to increase after rainfall interacted with the pine and hardwood canopies and were inversely related to both rainfall and through-fall depth. Oxidized N concentrations in streamflow were greatest during the rising limb of storm flow with subsequent decreases during the falling limb of storm hydrographs and lowest during base flow. The oxidized N inputs from bulk precipitation were considerably greater than outputs from streamflow resulting in a net retention of oxidized nitrogen within the watershed during the study period.     

NUTRIENT LOADS TO WISCONSIN LAKES: PART I. NITROGEN AND PHOSPHORUS EXPORT COEFFICIENTS1

ABSTRACT: Export coefficients (kg/km²/yr) for dissolved ortho-phosphate (OP), total phosphorus (TP), total inorganic nitrogen (TIN), and total nitrogen (TN) were derived for watersheds in Wisconsin using data bases available for 17 basins from the U.S. Environmental Protection Agency — National Eutrophication Survey, U.S. Geological Survey, and the Wisconsin Department of Natural Resources. Three general land use categories, representative of most regions in Wisconsin, were established: forest, mixed, and agricultural. Data for the 17 basins indicated greater exports of OP. TP, TIN, and TN as the percentage of forest decreased and agriculture increased. These region-specific coefficients are compared to the values reported in the literature representing much broader areas of the U.S.     

RELATION BETWEEN STREAM-WATER QUALITY AND GEOHYDROLOGY DURING BASE-FLOW CONDITIONS,ROBERTS CREEK WATERSHED,CLAYTON COUNTY,IOWA1

ABSTRACT: An investigation to determine the relation between stream water quality and geohydrology in the Roberts Creek watershed, Clayton County, Iowa, was conducted during selected base-flow periods in 1988–90. Discharge measurements were made and water samples collected for analyses of nutrients and selected herbicides in 19 subbasins along the main stem and tributaries of Roberts Creek. The areal extent of unconsolidated and bedrock units subcropping in each subbasin was quantified. The hydrologic data were correlated statistically with the geologic data to determine relations. Roberts Creek generally gained water and had larger nitrogen concentrations in subbasins in which bess and alluvial material were underlain primarily by low-permeability till and shale units. Roberts Creek generally lost water and had lower nitrate concentrations in subbasins with subcroppmg karstic units. Nitrogen concentrations decreased in streams underlain by the karstic units because the nitrogen removed by biological processes was not replaced by ground-water inflow. Seepage from Roberts Creek to ground water in areas of subcropping karstic carbonate rocks reduced the flow, which reduced the velocity, causing increased residence time of water in the stream. The additional residence time may allow additional time for biological processes to remove nitrogen from solution. There was no significant relation between dissolved orthophosphate or atrazine and the underlying geology.     

UNCERTAINTY ANALYSIS OF BMP EFFECTWENESS FOR CONTROLLING NITROGEN FROM URBAN NONPOINT SOURCES1

ABSTRACT: The effectiveness of urban Best Management Practices (BMPs) in achieving the No-Net-Increase Policy (NNTP), a policy designed to limit nonpoint nitrogen loading to Long Island Sound (US), is analyzed. A unit loading model is used to simulate annual nitrogen exported from the Norwalk River watershed (Connecticut) under current and future conditions. A probabilistic uncertainty analysis is used to incorporate uncertainty in nitrogen export coefficients and BMP nitrogen removal effectiveness. The inclusion of uncertainty in BMP effectiveness and nitrogen export coefficients implies that additional BMPs, or BMPs with a greater effectiveness in nitrogen removal, will be required to achieve the NNIP. Even though including uncertainty leads to an increase in BMP implementation rates or BMP effectiveness, this type of analysis provides the decision maker with a more realistic assessment of the likelihood that implementing BMPs as a management strategy will be successful. Monte Carlo simulation results indicate that applying BMPs to new urban developments alone will not be sufficient to achieve the NNIP since BMPs are not 100 percent effective in removing the increase in nitrogen caused by urbanization. BMPs must also be applied to selected existing urban areas. BMPs with a nitrogen removal effectiveness of 40–60 percent, probably the highest level of removal that can be expected over an entire watershed, must be applied to at least 75 percent of the existing urban area to achieve the NNIP This high rate of application is not likely to be achieved in urbanized watersheds in the LIS watershed; therefore, additional point source control will be necessary to achieve the NNIP     

PREDICTION OF CHLOROPHYLL A CONCENTRATIONS IN FLORIDA LAKES: THE IMPORTANCE OF PHOSPHORUS AND NITROGEN1

ABSTRACT: Models for the prediction of chlorophyll a concentrations were developed and tested using data on 223 Florida lakes. A statistical analysis showed that the best model was log (Chl a) =?2.49 + 0.269 log (TP) + 1.06 log (TN) or log (Chl a) =?2.49 + 1.06 log (TN/TP) + 1.33 log (TP) where Chl a is the chlorophyll a concentration (mg m^-3), TP is the total phosphorus concentration (mg m^-3) and TN is the total nitrogen concentration (mg m^-3). The model yields unbiased estimates of chlorophyll a concentrations over a wide range of lake types and has a 95 percent confidence interval of 29–319 percent of the calculated chlorophyll a concentrations. Other models, especially the published Dillon-Rigler and Jones-Bachmann phosphorus-chlorophyll models, are less precise when applied to Florida lakes. The data support the hypothesis that nitrogen is an important limiting nutrient in hypereutrophic lakes.