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38 MAYLAND ET AL. <br />riches Se in wet depositional fluxes to western Atlantic surface waters. They <br />measured an average of 30 and 170 ng Se/L in rainwater samples collected <br />over Bermuda and Lewes, DE, respectively. On occasion, values as high as <br />300 ng Se/L were encountered over the Lewes site. They calculated that the <br />wet depositional flux at Lewes, DE, was about 15 ng Se/cm2 per year (given <br />as 190 pmol/cm2 per year). That amount is equivalent to 1.5 g Se/ha an- <br />nually, which is about one-tenth the amount of fertilizer Se that is applied <br />annually in Se-deficient areas such as Finland and New Zealand. The wet <br />depositional flux calculated by Cutter and Church (1986) falls between the <br />values estimated by Ross (1985) for remote continental (75 pmol/cm2 per <br />year) and urban (840 pmol/cm2 per year) wet deposition. <br />Selenium's oxidation state in precipitation may be a sensitive oxidation- <br />reduction (redox) tracer (Cutter & Church, 1986). The authors found that <br />the range of selenite/selenate values was generally small [Se(IV)/5e(VI) _ <br />1.26 ± 0.95]. Two samples with the highest selenite/selenate ratios (15-20) <br />came from storms traveling in northerly directions, placing the coal-fired <br />Indian River Station power plant 30 km upwind of the rain sampler. They <br />calculated an apparent redox intensity of the precipitation, but suggested that <br />more data were needed to accurately determine the oxidation intensity of <br />air masses. <br />Andren et al. (1975) reported that Se in the fly ash and aerosols retrieved <br />from the Allen Steam Plant was all in the elemental form (Se °). Cutter and <br />Church (1986) detected selenide plus elemental Se in only one sample account- <br />ing for 28~Io of the total Se. The remaining (72%) Se occurred as selenite <br />and selenate. Fly ash has been shown to contain sufficient concentrations <br />of bioavailable Se that it could serve as a supplemental nutrient source for <br />plants and animals (Furr et al., 1975, 1976a, 1977, 1978). <br />Suzuki et al. (1981) and Cutter (1978) reported that selenite was the major <br />Se species in rainwater samples collected in Japan and on the California coast. <br />Robberecht and van Grieken (1980) reported variable quantities of both <br />selenite and selenate in the rain and snow samples collected from an urban <br />area in Belgium. <br />Bioavailability of Aerosol Selenium <br />The chemical speciation of Se and the particle size of the carrier aerosol <br />are important in assessing its bioavailability. Oral ingestion is the primary <br />route of entry into the animal body for most trace elements, although in- <br />halation of Pb may be an important route for body Pb loads. Aerosols may <br />enter the body through the respiratory system and serve as another source <br />of Se. While the larger 1 to 20 µm MMAD particles are deposited primarily <br />in the nasal and bronchial region of the respiratory system, the submicron <br />particles are deposited predominantly in the lungs and have the greatest en- <br />richment in many of the trace elements, including Se (Campbell et al., 1978). <br />Medinsky et al. (1981) modeled the distribution and retention of Se in <br />rats after inhalation of elemental Se and selenious acid aerosols (0.6 µm <br />MMAD). They noted that the rate of absorption of these two Se forms into <br />