Subject: Mold on stone
Shelley Reisman Paine <shelley [at] srpaine__com> writes >I am working on a set of oversize outdoor sculpture made from >Carrara marble. The sculpture stood outdoors for sixty years. After >it was vandalized in 2000 the owner stored them for five years in 4 >crates (9.5 feet x 4 feet x 4 feet) filled with straw. While in >storage large dark gray areas developed. Mary Lou Florian >identified the material as alternaria or cladosproium. The fungal >structures are not normal hyphae but sclerotic--heavily pigmented >(melanin) hyphae. As you reported, the cause for the microbially induced damage has already been identified by a microbiologist as two different fungi (alternaria and cladosporium) with heavily melanised reproductive structures. I would therefore rather concentrate on these microorganisms than exploring if the staining could be due to the presence of pigment-producing bacteria. However, this does not mean that these bacteria may not be present, as they have frequently been isolated from outdoor stone monuments. In fact, the microbial community of stone surfaces is always an interaction of many different microorganisms. Alternaria and Cladosporium are very common fungi and their reproductive structures are nearly everywhere. Therefore, it is not surprising to find that they grew heavily when the statute was packed with straw, which provides better growing conditions for these fungi than dry stone surfaces that are exposed to sunlight. The question is whether you really need to kill the fungi, as the change in climate provided by unpacking the sculpture, will most likely be enough to stop further growth (in fact the sculpture survived for 60 years without significant fungal growth before being packed). Further, a lot of conservation procedures will have fungicidal action (e.g. treatment with 70% ethanol or other organic solvents). However, you need to keep in mind that even when the fungal structures are dead, they will still be a health hazard. Dead fungal spores, when getting into your lungs, will still be recognized as a foreign substance and may cause an allergic reaction. Hence, when removing the fungal structures, appropriate protective clothing and removal of the contaminated air is necessary. Some attempts have been made with brushing and vacuuming (don't forget HEPA filters) with micro-nozzles under a stereo microscope. You will most likely not be able to remove the fungal structures entirely, as some of the hyphae may penetrate fairly deep into the stone (up to a few centimeters, depending on the condition and porosity of the stone). The other question is how to remove the dark stains, which is rather an aesthetical question than a matter of biodeterioration. I have not read Delgado Rodrigues paper (as that particular issue of Studies in Conservation is missing from our library). However, I am sure that you will get useful information from this article. Further, I am aware of a project at the Metropolitan Museum, on removing melanised fungi from paper. The aim of the project was "identifying the species present and developing 'designer' enzymes that can effectively and safely remove the disfiguring stains associated with them." as reported in Met Objectives in Spring 2002, which can be found at <URL:http://www.metmuseum.org/ Works_of_Art/objects_conservation/ mo_pdf/objective_spring2002.pdf>. **** Moderator's comments: The above URL has been wrapped for email. There should be no newline. Further, dark stains on white marble sounds like the ideal situation for laser cleaning. Potentially, the dark biological structures will strongly absorb the laser radiation, while the white marble will reflect it. I did some laser tests on biological growth on stone samples from temples of Angkor in Cambodia (different stone and microorganisms), and I had relatively good results. In cases where the biological growth could not be removed, it was bleached, giving at least a more satisfying aesthetical appearance. I hope this helps. And please report on your method if you have any success! Stefanie Scheerer Microbiology Dept. Cardiff University PO Box 915 Cardiff CF10 3TL Wales UK *** Conservation DistList Instance 19:26 Distributed: Saturday, November 19, 2005 Message Id: cdl-19-26-007 ***Received on Friday, 11 November, 2005