Water and sediment quality in threetidal bayous located near Pensacola, Florida, wereassessed during 1993–1995. The primary objective wasto determine the environmental condition of therelatively small urban bayous by comparing thechemical quality of the sediments and surface waterwith published guidelines and criteria developed toprotect marine life. Surface water concentrations ofmost potential toxicants such as heavy metals,organochloride pesticides, PAHs and PCBs were usuallybelow method detection limits. The major exception tothis trend was for copper which consistently exceededFlorida and National acute and chronic water qualitycriteria. Nickel, cadmium and chromium intermittentlyexceeded these criteria. Sediment contamination wassite-specific and chemically diverse. Theconcentrations of as many as 17 compounds exceededproposed Florida sediment quality assessmentguidelines indicating the potential for adversebiological effects. Nutrient concentrations, with oneexception, were below average levels found in otherFlorida estuaries. Seasonal variation in contaminantconcentrations for sediment collected from the samesampling station was less than an order of magnitude. The differences in the concentrations of the sameanalytes as measured for the multiple samplingstations located within the same bayou varied 1 to 2orders of magnitude and over 2 orders of magnitude forthe 20 sampling stations located in the three bayous. A within-bayou sediment contaminant gradient wasevident; sediment quality generally improved seaward.

Air monitoring stations were set up at 2 sites in the southern hemisphere — Moody Brook, Falkland Islands (51° 25′ S, 57° 56′W) and Halley, Research Station, Antarctica (75° 35′ S, 26° 30′ W). PCBs were monitored at the stations throughout 1999. Highest concentrations were observed when temperatures were greater. In general, concentrations were greater at Moody Brook than at Halley, although the difference in concentrations between sites was less for more chlorinated congeners. Air concentrations at both sites were compared with samples collected nearby over-water. Over water air concentrations were found to be greater than over land air concentrations. Concentrations were also compared with literature data for air concentrations at a remote site in the Canadian Arctic. Atmospheric concentrations of tri-chlorinated biphenyls were found to be approximately double those reported for Ellesmere Island in the Canadian Arctic, whilst concentrations in samples from Antarctica were very similar to those found in the high Arctic. Most other PCBs were a factor of 2–4 greater in the Canadian Arctic.

Results from the photolysis ofo, p-dichlorobenzene, bromobenzene, andp-dibromobenzene in water ice are reported. All phototransformations appeared to be based on dehalogenation, coupling, and rearrangement reactions in ice cavities. No photosolvolysis products, i.e. products from intermolecular reactions between organic and water molecules, were found. Many of the products were very toxic substances of a high environmental risk, such as PCBs. The results support our model, in which secondary, very toxic, pollutants can be formed in ice, snow, and atmospheric ice particles from primary pollutants through the action of solar irradiation. The photoproducts may be released to the environment by ice melting and evaporation.