Observations and Modeling of Stream Plunging in an Urban Lake1

Owens, Emmet M., Steven W. Effler, Anthony R. Prestigiacomo, David A. Matthews, and Susan M. O’Donnell, 2012. Observations and Modeling of Stream Plunging in an Urban Lake. Journal of the American Water Resources Association (JAWRA) 48(4): 707‐721. DOI: 10.1111/j.1752‐1688.2012.00646.x Abstract: The plunging behavior of two tributaries in Onondaga Lake, New York, is quantified based on a program of monitoring, process studies, and modeling. The dynamics of buoyancy of the tributaries are resolved with hourly measurements of temperature (T), specific conductance (SC), and turbidity (Tn) at the mouths, and observations every 6 h in the lake. Negative buoyancy of the tributaries is found to diminish and change rapidly during runoff events compared to dry periods. In‐lake patterns of the transport of plunging inflow are resolved for dry weather conditions using a dye tracer, and following a runoff event through measurements of T, SC, and Tn. The hydrodynamic/transport model ELCOM (Estuary Lake and Coastal Ocean Model) is demonstrated to perform well in simulating these patterns. Analyses conducted with the model establish the importance of diurnal effects and in‐lake mixing mediated by wind, the need for temporally detailed measurements during runoff events, and modifications of the plunging behavior of the urban tributary as it passes through a harbor. The model provides critical information to support rehabilitation programs for the lake by quantifying the transport of the two largest tributaries, particularly the distribution of the loads between the upper waters and stratified layers. The model predicts that 10% of the urban tributary load enters the upper waters of the lake within 24 h for a dry weather period; this portion increases to 30% for a runoff event.     

Integrative research on environmental and landscape change: PhD students' motivations and challenges

The growing demand for integrative (interdisciplinary or transdisciplinary) approaches in the field of environmental and landscape change has increased the number of PhD students working in this area. Yet, the motivations to join integrative projects and the challenges for PhD students have so far not been investigated. The aims of this paper were to identify the understanding of PhD students with regard to integrative research, their motivations to join integrative projects, their expectations in terms of integration and results, and to reveal the challenges they face in integrative projects. We collected data by a questionnaire survey of 104 PhD students attending five PhD Master Classes held from 2003 to 2006. We used manual content analysis to analyse the free-text answers. The results revealed that students lack a differentiated understanding of integrative approaches. The main motivations to join integrative projects were the dissertation subject, the practical relevance of the project, the intellectual stimulation of working with different disciplines, and the belief that integrative research is more innovative. Expectations in terms of integration were high. Core challenges for integration included intellectual and external challenges such as lack of knowledge of other disciplines, knowledge transfer, reaching depth, supervision, lack of exchange with other students and time demands. To improve the situation for PhD students, we suggest improving knowledge on integrative approaches, balancing practical applicability with theoretical advancement, providing formal introductions to other fields of research, and enhancing institutional support for integrative PhD projects.     

Removal of toxic ions (chromate, arsenate, and perchlorate) using reverse osmosis, nanofiltration, and ultrafiltration membranes

Rejection characteristics of chromate, arsenate, and perchlorate were examined for one reverse osmosis (RO, LFC-1), two nanofiltration (NF, ESNA, and MX07), and one ultrafiltration (UF and GM) membranes that are commercially available. A bench-scale cross-flow flat-sheet filtration system was employed to determine the toxic ion rejection and the membrane flux. Both model and natural waters were used to prepare chromate, arsenate, and perchlorate solutions (approximately 100 μg L⁻¹ for each anion) in mixtures in the presence of other salts (KCl, K₂SO₄, and CaCl₂); and at varying pH conditions (4, 6, 8, and 10) and solution conductivities (30, 60, and 115 mS m⁻¹). The rejection of target ions by the membranes increases with increasing solution pH due to the increasingly negative membrane charge with synthetic model waters. Cr(VI), As(V), and rejection follows the order LFC-1 (>90%) > MX07 (25–95%)  ESNA (30–90%) > GM (3–47%) at all pH conditions. In contrast, the rejection of target ions by the membranes decreases with increasing solution conductivity due to the decreasingly negative membrane charge. Cr(VI), As(V), and rejection follows the order CaCl₂ < KCl  K₂SO₄ at constant pH and conductivity conditions for the NF and UF membranes tested. For natural waters the LFC-1 RO membrane with a small pore size (0.34 nm) had a significantly greater rejection for those target anions (>90%) excluding (71–74%) than the ESNA NF membrane (11–56%) with a relatively large pore size (0.44 nm), indicating that size exclusion is at least partially responsible for the rejection. The ratio of solute radius (r_i,s) to effective membrane pore radius (r_p) was employed to compare ion rejection. For all of the ions, the rejection is higher than 70% when the r_i,s/r_p ratio is greater than 0.4 for the LFC-1 membrane, while for di-valent ions (, , and ) the rejection (38–56%) is fairly proportional to the r_i,s/r_p ratio (0.32–0.62) for the ESNA membrane.     

Individual particle characteristics of North African dust under different long-range transport scenarios

After urban sources, mineral dust in Madrid is the second biggest contributor to PM₁₀, making up 40% on average, of total emissions. Approximately, 50% of the days on which the daily limit of 50 μg m^?3 marked by the European Directive, are ascribable to Saharan outbreaks. The present study has focused on individual particle characterization of North African dust over Madrid by SEM/EDX, since no previous works on this type of characterization have been found in the region. More than 30,000 particles from 6 different samples have been measured to characterize 4 African episodes with very different meteorological scenarios, transport processes and source origins. Different samples from the same episode have also been characterized to evaluate homogeneity of dust characteristics over time. Silicates, mainly composed of clay minerals, are the main component, with abundances ranging from 65 to 85% by particle volume. Chemical cluster distribution of silicates has been linked to the major topsoil mineralogical composition in the origin of the episodes. Aspect Ratio (AR) has been used to compare particle morphology between episodes. AR values from samples taken under the same scenarios are statistically equal. For all the samples and size ranges AR values are found to be in the same order: AR_sulphates > AR_silicates > AR_carbonates. Particles not only maintained morphology during the episode, but also chemical composition, since clusters turned out to be very similar in samples taken on the same day and different days. Similarities and differences in particle chemical composition and morphology between the different transport patterns are discussed in detail throughout the paper.     

Catalysts and inhibitors for oxidative degradation of monoethanolamine

MEA solutions were subjected to oxidative degradation at both low and high gas rates. Solutions were degraded with 100 mL/min of 98%O₂/2%CO₂ with mass transfer achieved by vortexing. Solutions were analyzed for degradation products by IC and HPLC. In a parallel apparatus 7.5 L/min of 15%O₂/2%CO₂ was sparged through solution, with additional mass transfer achieved by vortexing. A Fourier Transform Infrared (FTIR) analyzer collected continuous gas-phase data on volatile products.Hydroxyethyl-formamide (HEF) and hydroxyethylimidazole (HEI) are the major liquid-phase oxidation products. In the presence of Fe²⁺ and Cu²⁺, HEF, HEI, and MEA losses increase by a factor of 3 compared to Fe²⁺ alone. Cr³⁺ and Ni²⁺, two metals present in stainless steel alloys, resulted in MEA losses that are 55% greater. In terms of oxidative degradation potential (greatest to lowest): Cu²⁺ > Cr³⁺/Ni²⁺ > Fe²⁺ > V⁵⁺.Inhibitor A reduces the formation of known products by 90% when catalyzed by Fe²⁺ and Cu²⁺ and by 99% with Cr³⁺/Ni²⁺. Inhibitor B reduces product rates by 97% and MEA losses by 75%, while a 100:1 ratio of EDTA to Fe²⁺ completely inhibits oxidation.     

Study of the spatial variation of the biodegradation rate of the herbicide bentazone with soil depth using contrasting incubation methods

Vertical and horizontal spatial variability in the biodegradation of the herbicide bentazone was compared in sandy-loam soil from an agricultural field using sieved soil and intact soil cores. An initial experiment compared degradation at five depths between 0 and 80 cm using sieved soil. Degradation was shown to follow the first-order kinetics, and time to 50% degradation (DT(50)), declined progressively with soil depth from 56 d at 0-10 cm to 520 d at 70-80 cm. DT(50) was significantly correlated with organic matter, pH and dehydrogenase activity. In a subsequent experiment, degradation rate was compared after 127 d in sieved soil and intact cores from 0 to 10 and 50 to 60 cm depth from 10 locations across a 160x90 m portion of the field. Method of incubation significantly affected mean dissipation rate, although there were relatively small differences in the amount of pesticide remaining in intact cores and sieved soil, accounting for between 4.6% and 10.6% of that added. Spatial variability in degradation rate was higher in soil from 0 to 10 cm depth relative to that from 50 and 60 cm depth in both sieved soil and intact core assessments. Patterns of spatial variability measured using cores and sieved soil were similar at 50-60 cm, but not at 0-10 cm depth. This could reflect loss of environmental context following processing of sieved soil. In particular, moisture content, which was controlled in sieved soil, was found to be variable in cores, and was significantly correlated with degradation rate in intact topsoil cores from 0 to 10 cm depth.     

Priority organic micropollutants in water sources in Flanders and the Netherlands and assessment of removal possibilities with nanofiltration

The occurrence of organic micropollutants in ground- and surface waters has become an important concern for the drinking water industry, mainly because of possible related health effects. Due to the polar nature of some of these pollutants, they are not completely removed by traditional water treatment barriers. This paper offers an overview of priority organic micropollutants and their occurrence in Flemish and Dutch water sources. Furthermore, rejection by nanofiltration is qualitatively predicted for the selected priority micropollutants. The qualitative prediction is based on the values of key solute and membrane parameters in nanofiltration. Predicted values are then compared with experimental values obtained from literature. Overall, the qualitative predictions are roughly in agreement with literature values. Prediction based on key parameters may thus prove to be a very quick and useful technique to assess the implementation of nanofiltration as a treatment step for organic micropollutants in drinking water plant design.     

Soil Aquifer Treatment (SAT) as a Natural and Sustainable Wastewater Reclamation/Reuse Technology: Fate of Wastewater Effluent Organic Matter (EfOM) and Trace Organic Compounds

Through the use of innovative analytical tools, the removal/transformation of wastewater effluent organic matter (EfOM) have been tracked through soil aquifer treatment (SAT). While the total amount of EfOM is significantly reduced by SAT, there are trends of shorter term versus longer term removals of specific EfOM fractions. The preferential removal of non-humic components (e.g., proteins, polysaccharides) of EfOM occurs over shorter travel times/distances while humic components (i.e., humic substances) are removed over longer travel times/distances, with the removal of both by sustainable biodegradation. Dissolved organic nitrogen (DON), a surrogate for protein-like EfOM, is also effectively removed over shorter term SAT. There is some background humic-like natural organic matter (NOM), associated with the drinking water source within the watershed, that persists through SAT. While most effluent-derived trace organic compounds are removed to varying degrees as a function of travel time and redox conditions, a few persist even through longer term SAT.     

Speciation/fractionation of nickel in airborne particulate matter: improvements in the Zatka sequential leaching procedure

Modifications are reported to the sequential leaching analytical method for nickel speciation/fractionation specified by Zatka so that larger sample masses can be analyzed. Improvements have been made in the completeness of the sulfide/metallic separation during the peroxide-citrate leach step by use of a larger volume of leachant, a longer leach duration and an orbital shaker. Minimal extraction of metallic nickel in this prolonged sulfidic nickel extraction has been confirmed. An increase in the number of samples analyzed simultaneously using these modifications has resulted in substantial productivity improvements and concomitant lower costs. It is critical for practitioners of sequential leaching techniques to recognize potential limitations and to use professional judgment when interpreting results. For example, results obtained may not be biologically relevant in assessing health risks; the acts of sampling and storage may result in changes in fractionation with time; surface coatings/films may alter the ability of a leachant to react with the target compound; and leaching behaviours may be different for samples differing only in particle size distributions.