# Multimodal machine learning and Raman spectroscopy uncover biochemical pathways of autumnal leaf senescence

**Authors:** Kieran R. Clark, Jarrod L. Thomas, Pola Goldberg Oppenheimer

PMC · DOI: 10.1186/s12870-026-08369-1 · 2026-02-17

## TL;DR

This study uses Raman spectroscopy and machine learning to uncover biochemical changes in oak leaves during autumnal senescence, revealing shifts in pectin forms and chlorophyll breakdown.

## Contribution

The study introduces a novel multimodal approach combining Raman spectroscopy, DFT calculations, and machine learning to explore biochemical pathways during leaf senescence.

## Key findings

- Raman-derived crystallinity increases from 0.185 in non-senescing to 0.594 in senescing leaves.
- Pectin shifts from α- to β-anomeric form as cellulose becomes more crystalline.
- Unique bond vibrations at 1490 and 1495 cm−1 indicate chlorophyll catabolism progression.

## Abstract

Quercus robur – the English oak, undergoes various complex biochemical changes during the process of senescence, one of the most significant being the catabolism of chlorophyll species. The full process of foliaceous ageing remains elusive and largely enigmatic. Here, we employed the use of Raman spectroscopy, density-functional theory calculation, spectrophotometry and colour channel analysis combined with an advanced artificial neural network, to explore senescence-induced biochemical changes to non-venous leaf tissue from Q. robur through the process of autumnal senescence. Our analysis demonstrates an increase of Raman-derived crystallinity from 0.185 in non-senescing leaves through to 0.594 in senescing leaves combined with a decrease of the intensity of the 854 cm− 1 peak and accompanying increase of the intensity of the 898 cm− 1 peak, which in totality suggests that pectin is moving from the α- to β- anomeric form as cellulose moves from an amorphous state into a more crystalline one. Further analysis indicates inconsistencies to the chlorophyll and carotenoid behaviours as leaves move from a non-senescent state to a fully senesced one, which combined with an unexpected increase to the 1215–1320 cm− 1 peak region in fully senesced tissue, suggests the presence of new Raman-active bond contributors in fully senesced tissue. Analysis of expected and predicted chlorophyll catabolites indicated the presence of unique bond vibration contributors at 1490 and 1495 cm− 1 in all senescence classes and 1510 cm− 1 in all senescence classes except in fully senesced tissue, highlighting both the progression of chlorophyll catabolism and potential further breakdown of late-stage catabolites. Classification via an advanced artificial neural network showed testing accuracies of 68.18% for non-senescent tissue, 83.40% for visually non-senescing tissue on minimally senesced leaves, 78.15% for visually non-senescing tissue on moderately senesced leaves, 94.15% for minimally senesced tissue, 99.20% for moderately senesced tissue and 100% for fully senesced tissue, yielding an overall differentiation accuracy of 88.50%. Insights obtained herein offer future avenues for both exploratory research and industrial application, namely the exploitation of foliar material for a high-value commercial and medicinal products.

The online version contains supplementary material available at 10.1186/s12870-026-08369-1.

## Linked entities

- **Species:** Quercus robur (taxon 38942)

## Full-text entities

- **Diseases:** chlorosis (MESH:D000747), fungal (MESH:D009181)
- **Chemicals:** tetrapyrroles (MESH:D045725), xylan (MESH:D014990), wax (MESH:D014885), bilin (MESH:D001654), alpha-amyrin (MESH:C000654244), carotenoid (MESH:D002338), D (MESH:D003903), pectin (MESH:D010368), hemicelluloses (MESH:C007916), chlorophyllide-a (MESH:C034388), digoxin (MESH:D004077), (C)-CH3] (-), phenylalanine (MESH:D010649), jasmonic acid (MESH:C011006), lignin (MESH:D008031), H (MESH:D006859), pheophorbide-a (MESH:C032623), C (MESH:D002244), chlorophyllin (MESH:C007020), chlorophyll-b (MESH:C037184), O (MESH:D010100), metal (MESH:D008670), steroids (MESH:D013256), carbohydrate (MESH:D002241), dioxobilin (MESH:C000590876), cellulose (MESH:D002482), hematinic acid (MESH:C090385), nitrogen (MESH:D009584), C-E- (MESH:D002563), pyropheophorbide-a (MESH:C040298), methylvinyl maleimide (MESH:C053515), aluminium (MESH:D000535), H2O (MESH:D014867), Chlorophyll (MESH:D002734), isoleucine (MESH:D007532), cardiac glycosides (MESH:D002301), SOL (MESH:D019904), pheophytin-a (MESH:C061694), Mg (MESH:D008274), CHO (MESH:C034482), ester (MESH:D004952)
- **Species:** Hordeum vulgare (barley, species) [taxon 4513], Acer platanoides (Norway maple, species) [taxon 4025], Quercus robur (English oak, species) [taxon 38942], Ocimum basilicum (basil, species) [taxon 39350], Liquidambar styraciflua (American sweet gum, species) [taxon 4400], Arabidopsis thaliana (mouse-ear cress, species) [taxon 3702], Ulmus glabra (species) [taxon 172265], Cercidiphyllum japonicum (species) [taxon 13413], Malus domestica (apple, species) [taxon 3750], Prunus armeniaca (apricot, species) [taxon 36596], Brassica napus (oilseed rape, species) [taxon 3708], Botrytis cinerea (gray fruit mold, species) [taxon 40559], PX clade (clade) [taxon 569578], Vitis vinifera (wine grape, species) [taxon 29760], Chenopodium album (common lambsquarters, species) [taxon 3559]
- **Mutations:** 1 C-C
- **Cell lines:** HOL — Hexagrammos otakii (Fat greenling), Spontaneously immortalized cell line (CVCL_YE20), MinSOL-H — Rattus norvegicus (Rat), Adenocarcinoma of the rat prostate, Cancer cell line (CVCL_Y658)

## Figures

4 figures with captions in the complete paper: https://tomesphere.com/paper/PMC13014873/full.md

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Source: https://tomesphere.com/paper/PMC13014873