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Biomedical subjects

Philip M Gschwend

Publications and source records attributed to Philip M Gschwend.

8 recordsLinked to original sources

Ferrous iron oxidation rates in the pycnocline of a permanently stratified lake.

Ferrous iron was found year round at 2-4 mM in the anoxic hypolimnion of the Halls Brook Holding Area (HBHA), a small lake in eastern Massachusetts. Oxygenated epilimnion waters always had total iron concentrations of <80 nanomolar, implying nearly complete oxidation of ferrous iron as it mixed upward across the lake's pycnocline. Assuming conductivity was a conservative parameter, and using data on the lake's water balance, upward advection rates (0.02-0.05 m d(-1)) and vertical eddy diffusion coefficients (0.007-0.05 m2 d(-1)) were determined for the lake's pycnocline on five dates. Using the same advection and diffusion parameters, corresponding pseudo first-order rate coefficients for ferrous iron oxidation, k(ox) (s(-1)), on those dates were calculated (0.0004-0.007 s(-1)). The values of k(ox) (s(-1)) were always too large to reflect only homogeneous solution reactions; and on at least four dates they appeared too fast to be due to heterogeneous catalysis on iron oxyhydroxides. This suggested that ferrous iron oxidation in this lake's pycnocline was primarily due to catalysis by microorganisms, and this was supported by comparison of azide-poisoned vs. untreated batch tests. As a result of their continuous production, iron oxyhydroxide precipitates and any associated sorbates/coprecipitates are most likely continuously settling back into the lake's deep water and bed sediments, except when episodic storm events flush these solids out of the pycnocline and downstream via the Aberjona River.

Boston↗

The electrostatic origin of Abraham's solute polarity parameter.

A computational method was developed which relates the empirical linear solvation energy relationship (LSER) solute polarity parameter, S (formerly denoted ), to two more fundamental quantities: a polarizability term and a computed solvent-accessible-surface electrostatic term. Electrostatics computations were conducted explicitly or with dielectric field polarizable continuum models (PCM, SCIPCM, IPCM), employing a density functional theory (B3LYP/6-311G(2df,2p)) or efficient Hartree-Fock (HF/MIDI!) method for 90 polar and nonpolar organic solutes. Electrostatic parameters calculated at electron isodensity solute surfaces were found to produce significantly better correlations with empirical S values than the same electrostatic parameters deduced from a fixed Bondi atomic radii based surface. The best-fit expression was found employing SCIPCM/IPCM at the 0.0004 e(-)/bohr(3) solvent-accessible-surface: S(fit)() = 0.46E - 0.091SigmaV(s)()(2), with squared correlation coefficient = 0.96 and standard deviation = 0.10, where E is a measured solute excess polarizability scale and SigmaV(s)()(2) is a quantum-calculated solute electrostatic descriptor in kcal A/mol. The resulting model is more accurate than previously developed estimation approaches and relies on only two fitted coefficients; it has the potential advantage of applicability to any solute composed of C, H, N, O, S, F, Cl, and Br. Finally, this investigation offers quantitative insight into the relative contributions of solute polarity and solute polarizability to the empirical LSER polarity parameter, S.

Journal Article↗

Estimating partition coefficients for fuel-water systems: developing linear solvation energy relationships using linear solvent strength theory to handle mixtures.

In many environmental transport problems, organic solutes partition between immiscible phases that consist of liquid mixtures. To estimate the corresponding partition coefficients, we evaluated the efficacy of combining linear solvation energy relationships (LSERs) developed for pure 1:1 systems via application of linear solvent strength theory. In this way, existing LSERs could be extended to treat solute partitioning from gasoline, diesel fuel, and similar mixtures into contacting aqueous mixtures. Unlike other approaches, this method allowed prediction of liquid-liquid partition coefficients in a variety of fuel-water systems for a broad range of dilute solutes. When applied to 37 polar and nonpolar solutes partitioning between an aqueous mixture and 12 different fuel-like mixtures (many including oxygenates), the root-mean-squared error was a factor of approximately 2.5 in the partition coefficient. This was considerably more accurate than application of Raoult's law for the same set of systems. Regulators and scientists could use this method to estimate fuel-water partition coefficients of novel additives in future fuel formulations and thereby provide key inputs for environmental transport assessments of these compounds.

Energy Transfer↗

A physical-chemical screening model for anticipating widespread contamination of community water supply wells by gasoline constituents.

Continuing modifications of fuels like gasoline should include evaluations of the proposed constituents for their potential to damage environmental resources such as subsurface water supplies. Consequently, we developed a screening model to estimate well water concentrations and transport times for gasoline components migrating from underground fuel tank (UFT) releases to typical at-risk community water supply wells. Representative fuel release volumes and hydrogeologic characteristics were used to parameterize the transport calculation. Subsurface degradation processes were neglected in the model in order to make risk-conservative assessments. The model was tailored to individual compounds based on their abundances in gasoline, gasoline-water partition coefficients (Kgw), and organic matter-water partition coefficients (Kom). Transport calculations were conducted for 20 polar and 4 nonpolar compounds found in gasoline, including methyl tert-butyl ether (MTBE) and other ether oxygenates, ethanol, methanol, and some aromatic hydrocarbons. With no calibration, the screening model successfully captured the reported magnitude of MTBE contamination of at-risk community supply wells. Such screening indicates that other oxygenates would cause similar widespread problems unless they were biodegradable. Stochastic analysis of field parameter variability concluded that community supply well contamination estimates had order-of-magnitude reliability. This indicated that such pre-manufacturing analyses may reasonably anticipate widespread environmental problems and/or inspire focused investigations into chemical properties (e.g., biodegradability) before industrial adoption of new fuel formulations.

Carcinogens, Environmental↗

Dependency of polychlorinated biphenyl and polycyclic aromatic hydrocarbon bioaccumulation in Mya arenaria on both water column and sediment bed chemical activities.

The bioaccumulation of polycyclic aromatic hydrocarbons (PAHs) and polychlorinated biphenyls (PCBs) by the filter-feeding soft-shell clam Mya arenaria was evaluated at three sites near Boston (MA, USA) by assessing the chemical activities of those hydrophobic organic compounds (HOCs) in the sediment bed, water column, and organisms. Polyethylene samplers were deployed to measure the activities of HOCs in the water column. Sediment activities were assessed by normalizing concentrations with sediment-water sorption coefficient values, including adsorption to black carbon in addition to absorption by organic carbon. Likewise, both lipids and proteins were considered in biota-water partition coefficients used to estimate chemical activities in the animals. Chemical activities of PAHs in M. arenaria were substantially less than those of the corresponding bed sediments in which they lived. In contrast, chemical activities of PCBs in M. arenaria often were greater than or equal to activities in the corresponding bed sediments. Activities of PAHs, such those of pyrene, in the water column were undersaturated relative to the sediment. However, some PCBs, such as congener 52, had higher activities in the water column than in the sediment. Tissue activities of pyrene generally were in between the sediment and water column activities, whereas activity of PCB congener 52 was nearest to water column activities. These results suggest that attempts to estimate bioaccumulation by benthic organisms should include interactions with both the bed sediment and the water column.

Adsorption↗

Reinterpreting literature sorption data considering both absorption into organic carbon and adsorption onto black carbon.

We hypothesized that the sorption of polycyclic aromatic hydrocarbons (PAHs) to natural sediments and soils should consider both absorption into a biogenic/diagenetic organic carbon (OC) fraction and adsorption onto a combustion-derived, black carbon (BC) fraction. Here, two sets of literature data were reevaluated to illustrate that an OC absorbent and a BC adsorbenttogether can (1) account for sediment--pore-waterdistribution coefficients observed in the field that are greater than predicted by a simple f(OC)K(OC) partitioning model and (2) explain a group of nonlinear phenanthrene isotherms observed in the laboratory with a single value for the BC-normalized distribution coefficient (log K(BC) = 6.1 i 0.04) and a Freundlich exponent (n approximately 0.6 if log K(OC) = 4.0) that is strongly dependent on the K(OC) value selected.

Absorption↗

Emission and fate assessment of methyl tertiary butyl ether in the Boston area airshed using a simple multimedia box model: comparison with urban air measurements.

Expected urban air concentrations of the gasoline additive methyl tertiary butyl ether (MTBE) were calculated using volatile emissions estimates and screening transport models, and these predictions were compared with Boston, MA, area urban air measurements. The total volatile flux of MTBE into the Boston primary metropolitan statistical area (PMSA) airshed was calculated based on estimated automobile nontailpipe emissions and the Universal Quasi-Chemical Functional-Group Activity Coefficient computed abundance of MTBE in gasoline vapor. The fate of MTBE in the Boston PMSA was assessed using both the European Union System for the Evaluation of Substances, which is a steady-state multimedia box model, and a simple airshed box model. Both models were parameterized based on the meteorological conditions observed during air sampling in the Boston area. Measured average urban air concentrations of 0.1 and 1 microg/m3 MTBE during February and September of 2000, respectively, were comparable to corresponding model predictions of 0.3 and 1 microg/m3 and could be essentially explained from estimated temperature-dependent volatile emissions rates, observed average wind speed (the airshed flushing rate), and reaction with ambient tropospheric hydroxyl radical (*OH), within model uncertainty. These findings support the proposition that one can estimate gasoline component source fluxes and use simple multimedia models to screen the potential impact of future proposed gasoline additives on urban airsheds.

Air Pollutants↗

Assessing the combined roles of natural organic matter and black carbon as sorbents in sediments.

We hypothesized that two mechanisms, absorption into natural organic matter and adsorption onto combustion-derived black carbon (BC), act in parallel to bind polycyclic aromatic hydrocarbons (PAHs) to Boston Harbor sediments. To focus on BC-adsorption, we removed the non-BC fraction by combusting near shore sediments at 375 degrees C for 24 h under air, leaving ca. 16% of the reduced carbon. The isotherm for pyrene sorption onto our combusted sediment was nonlinear with a Freundlich exponent of 0.62+/-0.12 and a BC-normalized distribution coefficient (microg/ kgBC)/(microg/L)n of 10(6.25)+/-0.14. Pyrene sorption to untreated sediment was reasonably estimated using Kd = f(oc) 10(4.7) + fBC 10(6.25) Cw(0.62-1) where f(oc) was the non-BC organic carbon content, 10(4.7) was the organic carbon-normalized absorption coefficient for pyrene (L/kg(oc)), fBC was the BC content, and Cw was the dissolved pyrene concentration (microg/ L). C/H/N ratios indicated that our environmental BC differed substantially from NIST diesel soot, possibly due to inclusion of larger BC particles from near source atmospheric fallout and urban runoff. The impact of BC on total PAH sorption may explain reports of nonlinear isotherms, Koc values for PAHs that exceed their respective Kow values, and discrepancies in bioavailability between planar and nonplanar sorbates.

Absorption↗