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Table 1 Assignment of different components of the cuticle. Wavenumbers derived from NMF

From: Raman imaging reveals in-situ microchemistry of cuticle and epidermis of spruce needles

Wavenumber (cm−1)

Assignment

Wax

Cutin

CaOx

1734

1723

 

ν C=O (fatty acid esters)

1712

1707

 

ν C=O (coumaric acid, midchain carbonyls)

 

1654

 

ν C=C (anthoxanthins)

1632

1634

 

ν C=C (coumaric acid, stilbenes); Φ8 (anthoxanthins)

1607

1607

 

Φ8 (all rings)

 

1570

 

ν C=O (anthoxanthins)

  

1488

ν C=O (Calcium oxalate) [107]

  

1463

ν C=O (Calcium oxalate) [107]

1455

  

δ C–H (aliphatic chains) [57]

1441

1440

 

δ C–H (aliphatic chains) [57]

1423

  

δ C–H (aliphatic chains) [57]

1372

  

γw CH2 (aliphatic chains) [57]

 

1362

 

Φ20a (anthoxanthins(A-ring))

 

1308

 

γt CH2 (aliphatic chains) [57]

1295

  

γt CH2 [57]

1201

1205

 

Φ7a (coumaricacid)

 

1177

 

Φ9a (anthoxanthins with p-subst. C-Ring)

1169

  

Φ9a (coumaric acid)

1123

  

ν C–C (aliphatic chains)

 

1112

  
 

1077

 

ν C–C (aliphatic chains)

1062

1066

 

ν C–C (aliphatic chains)

 

1001

 

Φ12 (stilbenes)

921

  

ν C–C (aliphatic chains)

  

895

νs C–C + δ O–C=O (Calcium oxalate) [107]

864

870

864

ν C–C + γr CH2 (aliphatic chains) [108]; (Calcium oxalate)

 

831

 

ν C–C + γr CH2 (aliphatic chains) [108]

 

738

 

(Kaempferol)

710

   

653

   

642

642

 

Φ6a (anthoxanthins (A-ring))

  

593

Water libration (Calcium oxalate) [107]

 

582

 

Φ1 (anthoxanthins (A-ring))

524

 

520

ν Ca-O + ν C–C (Calcium oxalate) [107]

 

518

 

Φ6b (anthoxanthins (A-ring))

  

503

 

418

414

  
  1. ν: stretching; δ: bending; γt: twisting; γr: rocking, γw: wagging; Φ: ring mode in Varsanyi notation [59]