Spectro-FLIM for heritage: scanning and analysis of the time resolved luminescence spectra of a fossil shrimp

Abstract We describe the use of a single-photon counting imaging device to scan the surface of a flat fossil specimen. We studied an Early Triassic shrimp identified as Anisaeger longirostrus , from the Paris Biota (Idaho, USA; ca 249.1 Ma). Chemically, the specimen consists of a polycrystalline material composed of relatively monodisperse transparent crystals about 10 µm in size. We collected time-resolved fluorescence spectra at each pixel along 300 µm wide ribbons at a rate of 10 µm per second with a spatial resolution of 1 µm × 10 µm. Fluorescence is excited along a line. We demonstrate the presence of two types of crystals whose luminescence significantly differs. The first type emits at 450 nm with a decay time of 840 ps. The second type contains two independent emission centres emitting at 437 nm and 490 nm. They exhibit multiexponential decays with lifetimes of 1 ns and more than 5 ns, respectively. Although a variable proportion of long emitters was observed, the fluorescence of the fossil appeared to be relatively uniform. Thus, over time, fossilization processes have therefore resulted in a homogeneous distribution of fairly pure crystals.

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Publication Details

Journal
Methods in microscopy
Published
2025-02-07
DOI
https://doi.org/10.1515/mim-2024-0020
Citations
1
Primary Topic
Random lasers and scattering media
Type
article
Field-Weighted Citation Impact
1.30

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article

Spectro-FLIM for heritage: scanning and analysis of the time resolved luminescence spectra of a fossil shrimp

Arnaud Brayard, Robert B. Pansu, Jean‐Frédéric Audibert, Emmanuel Fara et al.
1 citations
Methods in microscopy
Random lasers and scattering media
1.30
article

Spectro-FLIM for heritage: scanning and analysis of the time resolved luminescence spectra of a fossil shrimp

Arnaud Brayard, Robert B. Pansu, Jean‐Frédéric Audibert, Emmanuel Fara, Loïc Bertrand, Louis Patarin, Jérémie Ritoux
article en
1 citations

Abstract

Abstract We describe the use of a single-photon counting imaging device to scan the surface of a flat fossil specimen. We studied an Early Triassic shrimp identified as Anisaeger longirostrus , from the Paris Biota (Idaho, USA; ca 249.1 Ma). Chemically, the specimen consists of a polycrystalline material composed of relatively monodisperse transparent crystals about 10 µm in size. We collected time-resolved fluorescence spectra at each pixel along 300 µm wide ribbons at a rate of 10 µm per second with a spatial resolution of 1 µm × 10 µm. Fluorescence is excited along a line. We demonstrate the presence of two types of crystals whose luminescence significantly differs. The first type emits at 450 nm with a decay time of 840 ps. The second type contains two independent emission centres emitting at 437 nm and 490 nm. They exhibit multiexponential decays with lifetimes of 1 ns and more than 5 ns, respectively. Although a variable proportion of long emitters was observed, the fluorescence of the fossil appeared to be relatively uniform. Thus, over time, fossilization processes have therefore resulted in a homogeneous distribution of fairly pure crystals.

Methods in microscopyVol. 2(1)
Centre National de la Recherche Scientifique (FR), Université de Bourgogne (FR), Université Paris-Saclay (FR), CentraleSupélec (FR), Biogéosciences (FR)
Centre National de la Recherche Scientifique
Sustainable cities and communities
Openalex Percentile: Top 25%
Random lasers and scattering media
1.30
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Spectro-FLIM for heritage: scanning and analysis of the time resolved luminescence spectra of a fossil shrimp — Arnaud Brayard, Robert B. Pansu, et al. · Methods in microscopy (2025) | TGRS Research Map | TGRS