The Influence of Varying Algal Biomass On Contaminant Exposure in Benthic-Planktonic Mesocosms: Copper (Ii)

A series of mesocosms was exposed to a suite of light treatments and nutrient enrichment in order to generate algal communities of varying biomass. the influence of this biomass on the speciation of copper (II) was studied. Distribution coefficients (_Kd,Lkg-1) were relatively high (log_Kd = 5 to 7), indicative of robust trace metal sequestration, and were likely controlled by the particulate organic carbon content (foc). Differences in _Kd over time and among treatments were significant, as was the relationship between _Kd and foc. Fluorescence quenching was used to determine binding capacities (_Lt, M) and their associated binding constants (_Kcond,M^-1) in order to model the solid phase copper speciation. the _Kcond ranged between 2.1 and 5.2 × 10¹²M^-1, indicating a very strong copper-ligand complex, and was higher in mesocosms that received more light. the light _Lt increased over time, dramatically after the nutrient enrichment, but did not vary systematically among light treatments. _Lt ranged from 7.2 × 10- 7 to 4.9 × 10- 5 M. the large magnitudes of _Kd, _Kcond and _Lt ensured that greater than 97% of total copper in the mesocosms was complexed by organic matter. the total copper concentration ([Cu]_T, M) needed to reach a target dissolved copper concentration of 10^-12.5 M (pCu = 12.5) was determined for each mesocosm over time. [Cu]_T was between 8.02 × 10^-5 and 3.41 × 10^-2 M, and increased over time. the [Cu]_T normalized to the target pCu (Effective Dose Ratio, EDR) increased directly with increases in algal biomass, indicating a direct link between system productivity and copper exposure. Approximately 45% of the variance in EDR was explained by variance in total biomass, while the residual variance in EDR was due likely to differences in the strengths of particle associations and magnitude of binding capacities.     

Influence of Baltimore's Urban Atmosphere on Organic Contaminants over the Northern Chesapeake Bay

ABSTRACT

Air and precipitation samples were collected along an urban to over-water to rural transect across the northern Chesapeake Bay as a preliminary investigation into the spatial extent of elevated atmospheric concentrations of urban-derived persistent organic pollutants. Air samples were collected daily from June 3–9, 1996, along the transect as part of the Atmospheric Exchange over Lakes and Oceans project. Total (gas + particle bound) atmospheric polycy-clic aromatic hydrocarbon concentrations [∑-PAH] ranged from 0.4 to 114 ng/m³, and gas phase polychlorinated bi-phenyl concentrations [∑-PCB] ranged from 0.02 to 3.4 ng/m³. Strong concentration gradients were found for both PAHs and PCBs, with the highest concentrations in the city and the lowest at the downwind rural site. Gas and particle bound PAHs varied independently in the city, possibly due to strong but geographically separated emission sources. A precipitation event collected during westerly winds contained fourfold higher ∑-PAH and twelvefold higher ∑-PCB concentrations at the over-water site than at the rural background location, further indicating that the urban plume extends from Baltimore, MD, over the northern Chesapeake Bay over a spatial scale of approximately 30 km.     

Some Improvements in the Determination of Benzo [α] Pyrene in Air Samples

The earliest measurements of benz[α]pyrene (BαP) in air samples were almost exclusively based on chroma-tography on alumina columns followed by ultraviolet absorption, in spite of the fact that the original discovery and isolation of BαP in coal tar was based on its fluorescence properties. With the increasing use of fluorescence techniques, the vastly increased sensitivity over ultraviolet measurements has become generally apparent. In air sample extracts containing the four polycyclics, benzo[a]pyrene (BαP) benzo[k]-fluoranthene (BkF), benzo[g,h,i]perylene, (BghiP), and BαP, ultraviolet measurements for BαP are particularly, inaccurate. Fluorescence measurements of BαP are much more accurate, but some improvement in accuracy seems desirable. The present work deals with improvement of the fluorescence measurement of BαP. It now is possible to measure BαP in the presence of BkF with greatly increased accuracy. Interferences resulting from the presence of benzo[k]fluoranthene are now much lower.     

A side-by-side comparison of two systems of sequencing coupled reactors for anaerobic digestion of the organic fraction of municipal solid waste.

The objective of this work was to compare the performance of two laboratory-scale, mesophilic systems aiming at the anaerobic digestion of the organic fraction of municipal solid wastes (OFMSW). The first system consisted of two coupled reactors packed with OFMSW (PBR1.1-PBR1.2) and the second system consisted of an upflow anaerobic sludge bed reactor (UASB) coupled to a packed reactor (UASB2.1-PBR2.2). For the start-up phase, both reactors PBR 1.1 and the UASB 2.1 (also called leading reactors) were inoculated with a mixture of non-anaerobic inocula and worked with leachate and effluent full recirculation, respectively. Once a full methanogenic regime was achieved in the leading reactors, their effluents were fed to the fresh-packed reactors PBR1.2 and PBR2.2, respectively. The leading PBR 1.1 reached its full methanogenic regime after 118 days (Tm, time to achieve methanogenesis) whereas the other leading UASB 2.1 reactor reached its full methanogenesis regime after only 34 days. After coupling the leading reactors to the corresponding packed reactors, it was found that both coupled anaerobic systems showed similar performances regarding the degradation of the OFMSW. Removal efficiencies of volatile solids and cellulose and the methane pseudo-yield were 85.95%, 80.88% and 0.109 NL CH4 g(-1) VS(fed) in the PBR-PBR system; and 88.75%, 82.61% and 0.115 NL CH4 g(-1) VS(fed0 in the UASB-PBR system [NL, normalized litre (273 degrees K, 1 ata basis)]. Yet, the second system UASB-PBR system showed a faster overall start-up.