2014
DOI: 10.1007/s00339-014-8357-8
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Nonlinear imaging techniques as non-destructive, high-resolution diagnostic tools for cultural heritage studies

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Cited by 30 publications
(30 citation statements)
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“…In biomedical researches, SHG microscopy has emerged as a powerful technique to quantify collagen 3D organization in tissues, in particular in skin dermis 11,12 . NLO microscopy has recently been applied to the field of cultural heritage [13][14][15][16][17][18] but never to examine collagen-based objects. Nevertheless, this technique cannot resolve nanometer structural features of collagen and the image interpretation may be difficult on materials.…”
mentioning
confidence: 99%
“…In biomedical researches, SHG microscopy has emerged as a powerful technique to quantify collagen 3D organization in tissues, in particular in skin dermis 11,12 . NLO microscopy has recently been applied to the field of cultural heritage [13][14][15][16][17][18] but never to examine collagen-based objects. Nevertheless, this technique cannot resolve nanometer structural features of collagen and the image interpretation may be difficult on materials.…”
mentioning
confidence: 99%
“…These techniques under different modalities provide new insights for the assessment of appropriate conservation methods that have to be applied for various CH objects of high artistic or cultural significance [79,115]. Recent studies have demonstrated the potential of these techniques for depth resolved imaging of materials in cultural heritage, such as varnishes [79], lining glues [80,81], paintings [75], historical coatings [82], and corrosion layers on metal-based artifacts [84]. Fruitful key information concerning the determination of the different layers, precise thickness or surface topography, nature of the different materials, and cracks in the layers has been extracted.…”
Section: Non-linear Microscopymentioning
confidence: 99%
“…On the other hand, THG allows to resolve transparent interfaces, on the basis of local differences in refractive index and dispersion [8]. In Two-Photon-Excited Fluorescence (TPEF) the detection of fluorescence emitted after the simultaneous absorption of two infrared photons [9] yields to the identification of chromophores. Finally, fluorescence lifetime imaging microscopy (FLIM) measures time-decay of the fluorescence intensity exhibited by fluorescent emitting molecules [10], yielding information on the molecular microenvironment of a molecule and on its energy exchanges.…”
Section: Introductionmentioning
confidence: 99%