Backwater Confluences of the Ohio River: Organic and Inorganic Fingerprints Explain Sediment Dynamics in Wetlands and Marinas

In the Ohio River (OR), backwater confluence sedimentation dynamics are understudied, however, these river features are expected to be influential on the system’s ecological and economic function when integrated along the river’s length. In the following paper, we test the efficacy of organic and inorganic tracers for sediment fingerprinting in backwater confluences; we use fingerprinting results to evidence sediment dynamics controlling deposition patterns in confluences used for wetland and marina functions; and we quantify the spatial extent of tributary drainages with wetland and marina features in OR confluences. Both organic and inorganic tracers statistically differentiate sediment from stream and river end‐members. Carbon and nitrogen stable isotopes produce greater uncertainty in fingerprinting results than inorganic elemental tracers. Uncertainty analysis of the nonconservative tracer term in the organic matter fingerprinting application estimates an apparent enrichment of the carbon stable isotopes during instream residence, and the nonconservativeness is quantified with a statistical approach unique to the fingerprinting literature. Wetland and marina features in OR confluences impact 42% and 11% of tributary drainage areas, respectively. Sediment dynamics show wetland and marina confluences experience deposition from river backwaters with longitudinally linear and nonlinear patterns, respectively, from sediment sources.     

In situ push-pull method to determine ground water denitrification in riparian zones

To quantify ground water denitrification in discrete locations of riparian aquifers, we modified and evaluated an in situ method based on conservative tracers and 15N-enriched nitrate. Ground water was "pushed" (i.e., injected) into a mini-piezometer and then "pulled" (i.e., extracted) from the same mini-piezometer after an incubation period. This push-pull method was applied in replicate mini-piezometers at two Rhode Island riparian sites, one fresh water and one brackish water. Conservative tracer pretests were conducted to determine incubation periods, ranging from 5 to 120 h, to optimize recovery of introduced plumes. For nitrate push-pull tests, we used two conservative tracers, sulfur hexafluoride and bromide, to provide insight into plume recovery. The two conservative tracers behaved similarly. The dosing solutions were amended with 15N-enriched nitrate that enabled us to quantify the mass of denitrification gases generated during the incubation period. The in situ push-pull method detected substantial denitrification rates at a site where we had previously observed high denitrification rates. At our brackish site, we found high rates of ground water denitrification in marsh locations and minimal denitrification in soils fringing the marsh. The push-pull method can provide useful insights into spatial and temporal patterns of denitrification in riparian zones. The method is robust and results are not seriously affected by dilution or degassing from ground water to soil air. In conjunction with measurements of ground water flow-paths, this method holds promise for evaluating the influence of site and management factors on the ground water nitrate removal capacity of riparian zones.     

Passive flux meter measurement of water and nutrient flux in saturated porous media: bench-scale laboratory tests

The passive nutrient flux meter (PNFM) is introduced for simultaneous measurement of both water and nutrient flux through saturated porous media. The PNFM comprises a porous sorbent pre-equilibrated with a suite of alcohol tracers, which have different partitioning coefficients. Water flux was estimated based on the loss of loaded resident tracers during deployment, while nutrient flux was quantified based on the nutrient solute mass captured on the sorbent. An anionic resin, Lewatit 6328 A, was used as a permeable sorbent and phosphate (PO4(3-)) was the nutrient studied. The phosphate sorption capacity of the resin was measured in batch equilibration tests as 56 mg PO4(3-) g(-1), which was determined to be adequate capacity to retain PO4(3-) loads intercepted over typical PNFM deployment periods in most natural systems. The PNFM design was validated with bench-scale laboratory tests for a range of 9.8 to 28.3 cm d(-1) Darcy velocities and 6 to 43 h deployment durations. Nutrient and water fluxes measured by the PNFM averaged within 6 and 12% of the applied values, respectively, indicating that the PNFM shows promise as a tool for simultaneous measurement of water and nutrient fluxes.     

Determining long-term (decadal) deep drainage rate using multiple tracers

The deep drainage rate is a critical hydrological parameter in understanding contamination mechanisms of soil and groundwater. Little research has been conducted on the temporal variations in deep drainage rate during the last century. The objective of this study was to determine the long-term deep drainage rate on a cultivated loamy soil in the Canadian Prairies. Three tracers were used: KCl applied in 1971, fallout tritium in 1963, and NO3* released during the initial cultivation of the field (1923). Two soil cores to a depth of 3.6 m were taken along a flat portion of the field, and soil Cl(-), 3H, and NO3* concentrations were measured as a function of depth. An additional four cores were taken for soil water content measurements between 2000 and 2003. Distinct peaks in the depth distribution of these three tracers were located at 1.27 m for Cl(-), 1.31 m for 3H, and 1.52 m for NO3*, 32, 40, and 80 yr after the application of Cl(-), 3H, and NO3*, respectively. The average deep drainage rates, calculated as the product of the estimated tracer velocity and volumetric soil water content below the active root zone, were 2.0 mm yr(-1) from the Cl(-) tracer, 2.2 mm yr(-1) from 3H, and 2.5 mm yr(-1) from the NO3* tracer. Therefore, there was little temporal variability in the groundwater recharge over the eight decades that the field has been cultivated. The recharge rates are less than 1% of the mean annual precipitation (333 mm).     

Fracture-controlled nitrate and atrazine transport in four Iowa till units

Fractures in till may provide pathways for agricultural chemicals to contaminate aquifers and surface waters. This study was conducted to quantify the influence of fractures on solute fate and transport using three conservative and two nonconservative tracers. The conservative tracers were potassium bromide (KBr), pentafluorobenzoic acid (PFBA), and 1,4-piperazinediethanesulfonic acid disodium salt (PIPES); the nonconservative tracers were nitrate and atrazine [6-chloro-N-ethyl-N'-(1-methylethyl)-1,3,5-triazine-2,4-diamine]. Three sites in Iowa were investigated, including four late Wisconsinan and Pre-Illinoian tills. Laboratory tracer experiments were conducted using eight large (0.4-0.45 m long by 0.43 m in diameter), undisturbed columns of till collected from depths of 1 to 28 m. The tills were densely fractured, with fracture spacing ranging from 3.8 to 10.4 cm. First arrival velocities of Br- ranged from 0.004 to 64.8 m d(-1), 10 to 100 times faster than predicted for unfractured media. Nitrate behaved as a conservative tracer in weathered till columns, but degraded during experiments using deeper tills. Sorption caused retardation of atrazine in the shallowest four columns. Atrazine degradation occurred in deeper columns as demonstrated by deviations between atrazine and the conservative tracers. Mobile-immobile model (MIM) simulations estimated first-order exchange coefficients (alpha) ranging from 1 x 10(-8) to 1.7 x 10(-2) s(-1), sorption coefficients (K(d)) for atrazine ranging from 2.6 x 10(-5) to 1 x 10(-3) m3 kg(-1), and degradation half-lives ranging from 0.24 to 67 d (nitrate) and 1.6 to 277 d (atrazine). This study suggests that aquifers and surface waters associated with thin, fractured till units may be vulnerable to contamination, yet deeper aquifers may be protected by these materials due to increased residence times provided by matrix diffusion.     

Fluorescence imaging applied to tracer distributions in variably saturated fractured clayey till

The study of mechanisms controlling preferential flow and transport in variably saturated fractured clayey till is often hindered by insufficient spatial resolution or unknown measuring volume. With the objective to study these mechanisms while circumventing the obstacles, tracer experiments with two fluorescent tracers Acid Yellow 7 (AY7) and Sulforhodamine B (SB) were performed at three different rain events for a fall and a summer season. Irrigated areas were excavated down to depths of 2.8 m and the movement of both tracers in the exposed profiles was delineated simultaneously by high spatial resolution apparent concentration maps (pixel approximately 1 mm(2)) obtained with an imaging device. The device consists of a light source and a CCD camera, both equipped with tracer-specific-filters for fluorescent light. The fluorescence images were corrected for nonuniform lighting, changing surface roughness, and varying optical properties of the soil profile. The resulting two-dimensional apparent concentration distribution profiles of the tracers showed that: (i) relative low water content in the upper 10 cm of the irrigated till in summer had a pronounced retardation effect on the AY7-migration and no effect on the SB-migration; (ii) the dead-end biopores were not activated in the fall season; (iii) only 3D fracture-plans connected to hydraulically active 1D-biopores contributed to the leaching; (iv) the tracer migration primary followed macropores during both seasons, though AY7 also followed a topsoil piston transport in summer; (v) the highest tracer pixel apparent concentrations were often found in macropores and most pronounced in the summer season; and (vi) 3D-dilution in fractures seems to play a dominating role in AY7-migration in the fall season.     

Resolution and Analysis of Spatial Variations and Patterns in an Urban Lake with Rapid Profiling Instrumentation

Rapid response vertical profiling instrumentation was used to document spatial variability and patterns in a small urban lake, Onondaga Lake, associated with multiple drivers. Paired profiles of temperature, specific conductance (SC), turbidity (T_n), fluorometric chlorophyll a (Chl_f), and nitrate nitrogen (NO₃^?) were collected at >30 fixed locations (a “gridding”) weekly, over the spring to fall interval of several years. These gridding data are analyzed (1) to characterize phytoplankton (Chl_f) patchiness in the lake's upper waters, (2) to establish the representativeness of a single long‐term site for monitoring lake‐wide conditions, and (3) to resolve spatial patterns of multiple tracers imparted by buoyancy effects of inflows. Multiple buoyancy signatures were resolved, including overflows from less dense inflows, and interflows to metalimnetic depths and underflows to the bottom from the plunging of more dense inputs. Three different metrics had utility as tracers in depicting the buoyancy signatures as follows: (1) SC, for salinity‐enriched tributaries and the more dilute river that receives the lake's outflow, (2) T_n, for the tributaries during runoff events, and (3) NO₃^?, for the effluent of a domestic waste treatment facility and from the addition of NO₃^? solution to control methyl mercury. The plunging inflow phenomenon, which frequently prevailed, has important management implications.     

Hydrology of Clay Settling Areas and Surrounding Landscapes in the Phosphate Mining District,Peninsular Florida1

Abstract: The objective of this study was to use applied and naturally occurring geochemical tracers to study the hydrology of clay settling areas (CSAs) and the hydrological connectivity between CSAs and surrounding hydrological landscapes. The study site is located on the Fort Meade Mine in Polk County, Florida. The CSA has a well‐developed, subangular‐blocky, clay‐rich surface layer with abundant desiccation cracks and other macropores, and a massive, clay‐rich sublayer that is saturated below ～1.0‐2.5 m. A bromide tracer was applied to study hydrological processes in the upper part of the CSA. Bromide infiltrated rapidly and perched on a massive, clay‐rich sublayer. Bromide concentrations decreased in the upper part of the profile without being transported vertically down through the lower part of the profile suggesting that bromide was lost to lateral rather than to vertical transport. Infiltration and lateral flow were rapid suggesting that preferential flow through desiccation cracks and other macropores likely dominates flow in the upper part of the CSA. Naturally occurring solute and stable isotope tracers were used to study the hydrological connectivity between the CSA and the surrounding hydrological landscape. Three‐end mass‐balance mixing model results indicate that shallow and/or deep CSA water can be found in all downgradient waters and must be as much as ～50% of some downgradient waters. Discharge from the CSA to the surrounding surface water‐bodies and surficial aquifer occurs laterally through the berms and/or vertically through the massive, clay‐rich sublayer. However, the precise flow paths from the CSA to the surrounding hydrological landscape are unclear and the fluxes remain unquantified, so the precise effects of CSAs on the hydrology of the surrounding hydrological landscape also remain unquantified.     

Lessons learned from natural and industrial analogues for storage of carbon dioxide

The deployment of CCS (carbon capture and storage) at industrial scale implies the development of effective monitoring tools. Noble gases are tracers usually proposed to track CO₂. This methodology, combined with the geochemistry of carbon isotopes, has been tested on available analogues.At first, gases from natural analogues were sampled in the Colorado Plateau and in the French carbogaseous provinces, in both well-confined and leaking-sites. Second, we performed a 2-years tracing experience on an underground natural gas storage, sampling gas each month during injection and withdrawal periods.In natural analogues, the geochemical fingerprints are dependent on the containment criterion and on the geological context, giving tools to detect a leakage of deep-CO₂ toward surface. This study also provides information on the origin of CO₂, as well as residence time of fluids within the crust and clues on the physico-chemical processes occurring during the geological story.The study on the industrial analogue demonstrates the feasibility of using noble gases as tracers of CO₂. Withdrawn gases follow geochemical trends coherent with mixing processes between injected gas end-members. Physico-chemical processes revealed by the tracing occur at transient state.These two complementary studies proved the interest of geochemical monitoring to survey the CO₂ behaviour, and gave information on its use.     

The Use of Carbon and Nitrogen Isotopes to Study Watershed Erosion Processes1

Abstract:  Tracer studies are needed to better understand watershed soil erosion and calibrate watershed erosion models. For the first time, stable nitrogen and carbon isotopes (δ¹⁵N and δ¹³C) and the carbon to nitrogen atomic ratio (C/N) natural tracers are used to investigate temporal and spatial variability of erosion processes within a sub‐watershed. Temporal variability was assessed by comparing δ¹⁵N, δ¹³C, and C/N of eroded‐soils from a non‐equilibrium erosion event immediately following freezing and thawing of surface soils with two erosion events characterized by equilibrium conditions with erosion downcutting. Spatial variability was assessed for the equilibrium events by using the δ¹⁵N and δ¹³C signatures of eroded‐soils to measure the fraction of eroded‐soil derived from rill/interrill erosion on upland hillslopes as compared to headcut erosion on floodplains. In order to perform this study, a number of tasks were carried out including: (1) sampling source‐soils from upland hillslopes and floodplains, (2) sampling eroded‐soils with an in situ trap in the stream of the sub‐watershed, (3) isotopic and elemental analysis of the samples using isotope ratio mass spectrometry, (4) fractioning eroded‐soil to its upland rill/interrill and floodplain headcut end‐members using an unmixing model within a Bayesian Markov Chain Monte Carlo framework, and (5) evaluating tracer unmixing model results by comparison with process‐based erosion prediction models for rill/interrill and headcut erosion processes. Results showed that finer soil particles eroded during the non‐equilibrium event were enriched in δ¹⁵N and δ¹³C tracers and depleted in C/N tracer relative to coarser soil particles eroded during the equilibrium events. Correlation of tracer signature with soil particle size was explainable based on known biogeochemical processes. δ¹⁵N and δ¹³C were also able to distinguish between upland rill/interrill erosion and floodplain headcut erosion, which was due to different plant cover at the erosion sources. Results from the tracer unmixing model highlighted future needs for coupling rill/interrill and headcut erosion prediction models.     

Evaluating microbial purification during soil treatment of wastewater with multicomponent tracer and surrogate tests

Soil treatment of wastewater has the potential to achieve high purification efficiency, yet the understanding and predictability of purification with respect to removal of viruses and other pathogens is limited. Research has been completed to quantify the removal of virus and bacteria through the use of microbial surrogates and conservative tracers during controlled experiments with three-dimensional pilot-scale soil treatment systems in the laboratory and during the testing of full-scale systems under field conditions. The surrogates and tracers employed included two viruses (MS-2 and PRD-1 bacteriophages), one bacterium (ice-nucleating active Pseudomonas), and one conservative tracer (bromide ion). Efforts have also been made to determine the relationship between viruses and fecal coliform bacteria in soil samples below the wastewater infiltrative surface, and the correlation between Escherichia coli concentrations measured in percolating soil solution as compared with those estimated from analyses of soil solids. The results suggest episodic breakthrough of virus and bacteria during soil treatment of wastewater and a 2 to 3 log (99-99.9%) removal of virus and near complete removal of fecal coliform bacteria during unsaturated flow through 60 to 90 cm of sandy medium. Results also suggest that the fate of fecal coliform bacteria may be indicative of that of viruses in soil media near the infiltrative surface receiving wastewater effluent. Concentrations of fecal coliform in percolating soil solution may be conservatively estimated from analysis of extracted soil solids.     

Impact of preferential flow at varying irrigation rates by quantifying mass fluxes

Solute concentration and soluble dye studies inferring that preferential flow accelerates field-scale contaminant transport are common but flux measurements quantifying its impact are essentially nonexistent. A tile-drain facility was used to determine the influence of matrix and preferential flow processes on the flux of mobile tracers subjected to different irrigation regimes (4.4 and 0.89 mm h(-1)) in a silt loam soil. After tile outflow reached steady state either bromide (Br; 280 kg ha(-1)) or pentafluorobenzoic acid (PFBA; 121 kg ha(-1)) was applied through the irrigation system inside a shed (3.5 x 24 m). Bromide fluxes were monitored at an irrigation rate of 4.4 mm h(-1) while PFBA fluxes were monitored at an irrigation rate of 0.89 mm h(-1). At 4.4 mm h(-1) nearly one-third of the surface-applied Br was recovered in the tile line after only 124 mm of irrigation and was poorly fit by the one-dimensional convective-dispersive equation (CDE). On the other hand, the one-dimensional CDE fit the main PFBA breakthrough pattern almost perfectly, suggesting the PFBA transport was dominated by matrix flow. Furthermore, after 225 mm of water had been applied, less than 2% of the applied PFBA had been leached through the soil compared with more than 59% of the applied Br. This study demonstrates that the methodology of applying a narrow strip of chemical to a tile drain facility is appropriate for quantifying chemical fluxes at the small-field scale and also suggests that there may be a critical input flux whereby preferential flow is initiated.     

Assessing drilling mud and technical fluid contamination in rock core and brine samples intended for microbiological monitoring at the CO2 storage site in Ketzin using fluorescent dye tracers

The CO₂SINK project in Ketzin represents a field laboratory for the storage of CO₂ in a 650-m deep saline aquifer. The project is accompanied by a microbiological monitoring programme to characterise the composition and activity of the autochthonous microbial community in rock and brine samples and their changes in response to CO₂ storage. A prerequisite of these studies is the acquisition of samples free of contamination from microorganisms and organic and inorganic components. Drilling mud and technical fluids are the main sources of contamination. This study describes the application of the fluorescent dye tracers fluorescein and rhodamine B as contamination controls for rock core and brine samples. Fluorescein was added to drilling mud that was used during the coring phase of the Ketzin wells Ktzi 200, 201 and 202. In addition, total organic carbon (TOC) concentrations, reflecting the carboxymethyl cellulose (CMC) component of the drilling mud, were determined to verify the tracer results. The fluorescence and TOC analyses revealed that drilling mud filtrate penetrated the outer 20 mm of mildly permeable sandstone cores. Rhodamine B was added to brines that were used to displace the drilling mud and to flush the wells after completion. The tracer monitoring during the discharge of drilling mud and displacement brines from the wells during hydraulic tests and nitrogen lifts enabled the quantification of reservoir fluid quality. After the production of 140–190 m³ (16–21 borehole volumes) of fluid, the drilling mud concentration was reduced to about 0.05%. The use of fluorescein emerged as a field-capable, sensitive and reliable method during the sampling of rock core and formation brine samples.     

Micro-trench experiments on interflow and lateral pesticide transport in a sloped soil in northern Thailand

During recent decades, a change in land use in the mountainous regions of Northern Thailand has been accompanied by an increased input of agrochemicals. We identified lateral water flow and pesticide transport pathways and mechanisms in a Hapludult on a sloped litchi orchard in Northern Thailand. During two rainy seasons, two micro-trench experiments were performed at the plot scale (2 by 3 m). The first experiment was performed at the footslope of the orchard; the second was performed at a midslope position. Two salt tracers (bromide and chloride) and two pesticides {methomyl [S-methyl-N-(methylcarbamoyloxy)thioacetimidate] and chlorothalonil (2,4,5,6-Tetrachlor-1,3-benzdicarbonitril)} were applied in stripes parallel to the slope 150 and 300 cm away from the trench. At the trench, soil water was collected by wick samplers. Tensiometers and time-domain reflectometry probes were installed. At the end of the experiment, soil samples were taken and analyzed for residual concentrations of tracers and pesticides. Lateral subsurface flow of water occurred exclusively along preferential flow paths and was mainly observed at 0- to 30- and 60- to 90-cm depth. Lateral transport of pesticides was negligible, but both pesticides were found beneath the application area at 90 cm depth. Therefore, they may pose a groundwater contamination risk. The amount of wick flow and the location of interflow were mainly a function of rain amount and antecedent soil water suction. During dry periods, water flow was restricted to the topsoil. After heavy rain events and wet periods, interflow was mainly observed in the subsoil. The cumulative rain amount between samplings necessary to induce interflow was 20 mm. At the footslope, the interflow was seven times higher, and the network of water-bearing pores increased compared with the midslope position.     

Influence of flow rate on transport of bacteriophage in shale saprolite

The objective of this study was to investigate the influence of flow rate on transport and retention of bacteriophage tracers in a fractured shale saprolite, which is a highly weathered, fine-grained subsoil that retains much of the fabric of the parent bedrock. Synthetic ground water containing PRD-1, MS-2, and bromide was passed through a saturated column of undisturbed shale saprolite at rates ranging from 0.0075 to 0.96 m d '. First arrival of the bacteriophage tracers in effluent samples in each of the experiments occurred within 0.01 to 0.04 pore volumes (PV) of the start of injection, indicating that bacteriophage were advectively transported mainly through fractures or macropores. Bacteriophage transport velocities, based on first arrival in the effluent, were very similar to fracture flow velocities calculated using the cubic law for flow in a fractured material. For MS-2, maximum concentration and mass of tracer recovered both increased steadily as flow rate increased. For PRD-1, these values initially increased, but were nearly constant at flow rates above 0.039 m d(-1), indicating that approximately 50% of the observed losses were independent of flow rate. Evaluation of the data indicates that physical straining and electrostatic or hydrophobic attachment to fracture or macropore walls were the dominant retention processes. Inactivation and gravitational settling playing secondary roles, except at the slowest flow rates. The study suggests that microbial contamination from sources such as septic fields and sewage ponds may pose a threat to the quality of ground water and surface water in areas with saprolitic subsoils.     

RHODAMINE WT DYE LOSSES IN A MOUNTAIN STREAM ENVIRONMENT1

ABSTRACT: A significant fraction of rhodamine WT dye was lost during a short term multitracer injection experiment in a mountain stream environment. The conservative anion chloride and the sorbing cation lithium were concurrently injected. In-stream rhodamine WT concentrations were as low as 45 percent of that expected, based on chloride data. Concentration data were available from shallow‘wells’dug near the stream course and from a seep of suspected return flow. Both rhodamine WT dye and lithium were nonconservative with respect to the conservative chloride, with rhodamine WT dye closely following the behavior of the sorbing lithium. Nonsorption and sorption mechanisms for rhodamine WT loss in a mountain stream were evaluated in laboratory experiments. Experiments evaluating nonsorption losses indicated minimal losses by such mechanisms. Laboratory experiments using sand and gravel size streambed sediments show an appreciable capacity for rhodamine WT sorption. The detection of tracers in the shallow wells and seep indicates interaction between the stream and the flow in the surrounding subsurface, intergravel water, system. The injected tracers had ample opportunity for intimate contact with materials shown in the laboratory experiments to be potentially sorptive. It is suggested that in the study stream system, interaction with streambed gravel was a significant mechanism for the attenuation of rhodamine WT dye (relative to chloride).     

Determination of direct and fugitive PM emissions in a Mediterranean harbour by means of classic and novel tracer methods

Remodelling works are frequent in harbour areas, given that they must adapt to rapidly changing market requirements. Depending on their nature (construction, demolition, etc.), these works may be carried out during long periods of time and thus exert a significant impact on the air quality at the harbours and their surroundings. The air quality at the Valencia harbour was studied during an enlargement project. Four sampling stations aimed to cover the major dust-emitting activities in the harbour. In addition, a sampling campaign was carried out to collect dust materials at their emission sources (e.g., loading and unloading of clinker and petroleum coke, as well as the enlargement works). Differences obtained between PM levels at the monitoring sites were correlated with the distance between sampling stations and enlargement works and/or harbour operations, as well as with the preferential wind direction. In all cases, the days with the highest PM_10 levels were linked to wind directions coinciding with the location of the enlargement works or the clinker and petroleum coke stocks. Classic source apportionment methodologies (PCA and CMB) were applied to the data, but their interpretation was complex due to the similar chemical signatures of PM originating from direct and fugitive emissions from stocked materials (e.g., clinker), and the enlargement works. To overcome this difficulty, a novel non-statistical approach was used to obtain quantitative estimations of the contributions from sources (petroleum coke and clinker), based on the correlation between specific PM components (e.g., carbonaceous species) and source tracers (e.g., V). Finally, a qualitative test using phenolphthalein was devised to identify the presence of clinker on the filters, which provided positive results. This novel tracer approach is thus recommended for harbour authorities.     

TRANSIENT STORAGE ASSESSMENTS OF DYE‐TRACER INJECTIONS IN RIVERS OF THE WILLAMETTE BASIN,OREGON1

ABSTRACT: Rhodamine WT dye‐tracer injections in rivers of the Willamette Basin yield concentration‐time curves with characteristically long recession times suggestive of active transient storage processes. The scale of drainage areas contributing to the stream reaches studied in the Willamette Basin ranges from 10 to 12,000 km². A transient storage assessment of the tracer studies has been completed using the U.S. Geological Survey's One‐dimensional Transport with Inflow and Storage (OTIS) model, which incorporates storage exchange and decay functions along with the traditional dispersion and advection transport equation. The analysis estimates solute transport of the dye. It identifies first‐order decay coefficients to be on the order of 10^?5/sec for the nonconservative Rhodamine W.T. On an individual subreach basis, the first‐order decay is slower (typically by an order of magnitude) than the transient storage process, indicating that nonconservative tracers may be used to evaluate transient storage in rivers. In the transient storage analysis, a dimensionless parameter (A_s/A) expresses the spatial extent of storage zone area relative to stream cross section. In certain reaches of Willamette Basin pool‐and‐riffle, gravel‐bed rivers, this parameter was as large as 0.5. A measure of the storage exchange flux was calculated for each stream subreach in the simulation analysis. This storage exchange is shown subjectively to be higher at higher stream discharges. Hyporheic linkage between streams and subsurface flows is the probable physical mechanism contributing to a significant part of this inferred active transient storage. Hyporheic linkages are further suggested by detailed measurements of river discharge with an Acoustic Doppler Current Profiler system delineating zones in two large rivers where water alternately enters and leaves the surface channels through gravel‐and‐cobble riverbeds. Measurements show patterns of hyporheic exchange that are highly variable in time and space.     

A critical appraisal of PAH indices as indicators of PAH source and composition in Elelenwo Creek,southern Nigeria

The survey of polycyclic aromatic hydrocarbons (PAHs) and their relation to potential pollution sources were investigated in suspended particulate matter (SPM), surface waters, and sediments from Elelenwo Creek, southern Nigeria. Total PAH concentrations varied from 2,021.35 to 3,926.84 μg/kg dry weights in SPM and from 4,238.00 to 5,490.84 μg/kg dry weights in sediments. Furthermore, concentration levels of PAHs varied from 720.46 to 857.65 μg/l in the surface waters, which indicates that the aquatic ecosystem is polluted by PAHs. The 2, 3-ring PAHs were not dominant in SPM (34.73%), surface water (40.09%), and sediments (22.43%). While anthracene was more abundant, of the 2, 3-ring PAHs in SPM, the most abundant in the surface waters and sediments were fluorene and acenaphthylene. Four origin indices or concentration ratios of PAH isomer pairs were used to evaluate the suitability of these compounds as tracers to distinguish between the contamination arising from different sources. A critical appraisal of the PAH indices, therefore, suggested that biomass combustion is the major PAH source in the environmental matrices. Relative PAH patterns in the environmental matrices were also evaluated using principal component analysis, and were found to correlate with the PAH patterns of the different potential contamination sources.