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Major microorganisms in biofilms on external surfaces of historic buildings are algae, cyanobacteria, bacteria, and fungi. Their growth causes discoloration and degradation. We compared the phototrophs on cement-based renderings and limestone substrates at 14 historic locations (47 sites sampled) in Europe and Latin America. Most biofilms contained both cyanobacteria and algae. Single-celled and colonial cyanobacteria frequently constituted the major phototroph biomass on limestone monuments (32 sites sampled). Greater numbers of phototrophs, and especially of algae and of filamentous morphotypes, were found on cement-based renderings (15 sites), probably owing to the porosity and small pore size of the latter substrates, allowing greater entry and retention of water. All phototrophic groups were more frequent on Latin American than on European buildings (20 and 27 sites, respectively), with cyanobacteria and filamentous phototrophs showing the greatest differences. The results confirm the influence of both climate and substrate on phototroph colonization of historic buildings.

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Buildings at the important archaeological sites of Uxmal and Kabah, Mexico, are being degraded by microbial biofilms. Phospholipid fatty acid (PLFA) and chlorophyll a analyses indicated that phototrophs were the major epilithic microorganisms and were more prevalent on interior walls than exterior walls. Culture and microscopical techniques showed that Xenococcus formed the major biomass on interior surfaces, but the stone-degrading genera Gloeocapsa and Synechocystis were also present in high numbers. Relatively few filamentous algae and cyanobacteria were detected. The fatty acid analysis also showed that complex biofilms colonize these buildings. Circular depressions observed by scanning electron microscopy (SEM) on stone and stucco surfaces beneath the biofilm corresponded in shape and size to coccoid cyanobacteria. SEM images also demonstrated the presence of calcareous deposits on some coccoid cells in the biofilm. Phototrophic biofilms may contribute to biodegradation by (1) providing nutrients that support growth of acid-producing fungi and bacteria and (2) active "boring" behavior, the solubilized calcium being reprecipitated as calcium carbonate.

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This report describes the sequence of fungal colonization and the influence of biocide incorporation on paint films, determined using quantitative methods. Two buildings were painted with an acrylic paint, with and without an experimental biocide formulation containing a carbamate (carbendazin), N-octyl-2H-isothiazolin-3-one and N-(3,4-dichlorophenyl)N,N-dimethyl urea (total biocide concentration 0.25% w/w). One week after painting, the major groups of organisms detected were yeasts and Cladosporium. The yeast population fell to undetectable levels after the third week and this microbial group was not detected again until the 31st week, after which they increased to high levels on the 42nd week. Aureobasidium showed a pattern similar to the yeasts. The main fungal genera detected over the 42-week period were Alternaria, Curvularia, Epicoccum, Helminthosporium, Coelomycetes (mainly Pestalotia/Pestalotiopsis), Monascus, Nigrospora, Aureobasidium and Cladosporium. The latter was the main fungal genus detected at all times. The physiological factors controlling colonization are discussed. Cladosporium, Aureobasidium, Tripospermum and yeasts on the painted surfaces were all able to grow on mineral salts agar containing 10% sodium chloride. This is the first time that the genus Tripospermum has been reported on painted buildings. The fungal population on biocide-containing surfaces was significantly lower than on non-biocide-containing paint after 13 weeks and continued so to 42 weeks after painting, but there was no statistically significant difference in the level of fungal biodiversity.

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