Effects of season and low-level air pollution on physiology and element content of lichens from the U.S. Pacific Northwest.

Lichens were collected from three low-elevation sites in the western Cascade Range: HJ Andrews, OR (clean) and Bull Run, OR, and Pack Forest, WA (moderately enhanced nitrogen and sulfur deposition). The latter sites were within 50 km of Portland and Seattle/Centralia urban-industrial areas, respectively. Tissue concentrations of sulfur, nitrogen, and other macronutrients; rates of net carbon uptake; concentrations of photosynthetic pigments; and thallus density were correlated with season and seasonal changes in Platismatia glauca. Ion concentrations in precipitation and total wet deposition were measured from natural settings. Concentrations of depositional ions in precipitation, including NO3- and NH4+, were generally highest at Bull Run and Pack Forest; SO4(2-) concentrations and acidity were highest at Pack Forest. Total wet deposition was higher in the winter rainy season than the dry summer season at all three sites. Lichens adapted physiologically and morphologically to the higher light intensity and the warm, dry climate of summer through decreased optimal water content for CO2 uptake, increased concentrations of carotenoids and increased thallus density. Compared to the clean site, the sites with enhanced deposition were associated in P. glauca with year-round higher tissue concentrations of N, S, K, and Na; higher concentrations of total chlorophyll and carotenoids; higher OD435/415 ratios; higher CO2 uptake and lower thallus density in summer; and a general absence of other sensitive lichens. These results indicate that moderate levels of fertilizing air pollutants can stimulate carbon uptake and provide protection against chlorophyll degradation in air pollution-tolerant lichens of the Pacific Northwest, especially during the dry summer season.

Characterization of a major cell wall antigen and potential adhesin in three strains of Candida albicans.

Selected strains of Candida albicans were examined to reveal the surface antigenicity and biochemical nature of major cell wall proteins that also were shown to serve as cellular adhesins on human buccal epithelial cells. Confirmation of the adhesive properties of these cells was made by scanning electron microscopy and immunofluorescence microscopy. Particular attention was directed at the clinical isolate KM-302. By means of indirect immunofluorescence staining, the KM-302 blastoconidia absorbed rabbit anti-C. albicans ATCC-32354 serum, revealing specific localization of surface antigens on germ tubes and pseudohyphae. Extracellular polymeric material and the cell wall extract of C. albicans KM-302 blastoconidia were found to contain a major surface antigen of 49 kDa that exhibited 42% adhesion inhibition in vitro. Of considerable significance is that immunogold localization by electron microscopy showed the antigen to be almost exclusively cell wall bound. This major antigen, identified in affinity and gel filtration chromatography fractions, was composed of 4% carbohydrate and 95.7% protein and had an isoelectric point of 6.1. The major antigen also showed a high level of similarity with that of C. albicans strain SC-5314 inasmuch as the major antigen of that strain had carbohydrate and protein compositions of 4 and 95.5%, respectively. Both of these strains also possessed the same percent of adhesion inhibition on human buccal epithelial cells.