Isolation and Identification of Fungal Species and Scientific Preservation of World Heritage: Case of Fatehpur Sikri, Uttar Pradesh, India

Author:

Gupta Sanjay PrasadORCID,Agnihotri Sachin KumarORCID

Abstract

Fungi play a considerable role for the deterioration and widely recognized as major bio-deteriogens of cultural heritage depending on climatic conditions, humidity level and surface material for fungal colonization. The weathering of stone monuments is significantly increased by endolitic fungi. Fungi can deteriorate different substrates via various physical and chemical mechanisms. Hyphal growth and penetration into the substrate can cause symptoms like discoloration, bio-pitting, cricketing, exfoliation and patina formation. On the other hand, chemical mechanism includes acid secretion, release of extracellular enzymes, pigment production, oxidation/reduction reaction reactions and secondary mycogenic minerals formation. These process can lead to serious, both esthetic and structural alterations which may be irreversible and could permanently impair artwork. Proper isolation and identification of fungi by different microscopic technique and in vitro biodegradation tests are pivotal in understanding complex bio-deterioration mechanism caused by fungal deteriogens. Bio-deterioration and bio-degradation studies require multidisciplinary approach and close collaboration of microbiologists, chemists and different personnel responsible for safeguarding of cultural property and artifacts, especially restorers and conservators. This article provides information on fungi infesting historical monument of Fatehpur Sikri and their management by biocidal compounds. Present investigation was conducted to evaluate the status of fungal decay of stone monuments of Fatehpur Sikri. A total of 06 fungal species were isolated from colored stains, patinas and biofilms produced on the surfaces of monuments of Fatehpur Sikri due to mechanism of bio-deterioration. The fungal species Alternaria alternata, Aspergillus fumigatus, Aspergillus flavus, Aspergillus niger, Cladosporium herbarum, and Rhizopus oryzae were prevalent.

Publisher

AMO Publisher

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