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. 2021 Jul 15;17:78. doi: 10.1186/s13007-021-00781-y

Table 1.

Summary table of reported to date Raman studies on botanicals

Target Objective Instrumentation/parameters Peaks with increase in intensity Peaks with decrease in intensity Conclusion
Disease diagnostics
 Tomato, leaf Liberibacter disease in tomatoes [8] Handheld spectrometer (λ = 830 nm; P = 495 mW; T = 1 s) 747 cm−1 (pectin); 1000, 1115, 1155, 1184, 1218 and 1525 cm−1 (carotenoids) Liberibacter disease in tomatoes is associated with degradation and fragmentation of host carotenoids and pectin
 Orange and grapefruit, leaves Huanglongbing (HLB) or citrus greening [23] Handheld spectrometer (λ = 830 nm; P = 495 mW; T = 1 s) 1601–1630 cm−1 (phenylpropanoids; 1440–1455 cm−1 (aliphatic) 1184 and 1218 cm−1 (xylan, carotenoids); 1525 cm−1 (carotenoids), as well as 1288 cm−1 (aliphatic); 1155 and 1326 cm−1 (cellulose) HLB is associated with an increase in phenylpropanoids and decrease in xylan, carotenoids and cellulose
 Orange and grapefruit, leaves Nutrient deficiency in citrus trees [23] Handheld spectrometer (λ = 830 nm; P = 495 mW; T = 1 s) 1247, 1601–1630 cm−1 (phenylpropanoids; 1440–1455 cm−1 (aliphatic) 1184 and 1218 cm−1 (xylan, carotenoids) ND is associated with an increase in phenylpropanoids
 Orange, leaf Canker [22] Handheld spectrometer (λ = 830 nm; P = 495 mW; T = 1 s) 1601–1630 cm−1 (phenylpropanoids) Canker is associated with a decrease in phenylpropanoids content
 Orange, leaf HLB and blight [22] Handheld spectrometer (λ = 830 nm; P = 495 mW; T = 1 s) Diagnostics was achieved via the use of PLS-DA
 Wheat, grain Ergot [15] Handheld spectrometer (λ = 1064 nm; P = 200 mW; T = 30 s) 1650 and 1667 cm−1 (proteins) ergot infection may be associated with expression and deposition of alpha-helical and beta-sheet proteins
 Wheat, grain Black tip [15] Handheld spectrometer (λ = 1064 nm; P = 200 mW; T = 30 s) 1348 cm−1 (monomeric sugars) and 1600 cm−1 (lignin); shift of 862 peak to 856 cm−1 (pectin) 862 and 937 cm−1 (starch) black tip may degrade lignin and ferment starch into monomeric sugars; esterification of pectin
 Sorghum, grain Mold [15] Handheld spectrometer (λ = 1064 nm; P = 200 mW; T = 30 s) shift of 856 peak to 862 cm−1 (pectin); change in ratio between 1518 cm−1 and 1541 cm−1 peaks (carotenoids) 1600 and 1630 cm−1 (phenylpropanoids) Degradation of phenylpropanoids; a decrease in methylesterfication of pectin caused by the infections; suggest a decrease in the length of conjugated double bonds of carotenoids
 Sorghum, grain Ergot [15] Handheld spectrometer (λ = 1064 nm; P = 200 mW; T = 30 s) 1150, 940, 1124 and 1083 cm−1 (monomeric sugars); shift of 856 peak to 862 cm−1 (pectin); change in ratio between 1518 cm−1 and 1541 cm−1 peaks (carotenoids) 1600 and 1630 cm−1 (phenylpropanoids) ergot hydrolyzes starches to produce monomeric sugars; a decrease in methylesterfication of pectin caused by the infections; suggest a decrease in the length of conjugated double bonds of carotene
 Maize, grain Fusarium spp [16] Handheld spectrometer (λ = 1064 nm; P = 200 mW; T = 30 s) 1658 cm−1 (protein); 1153 cm−1 (starch) 1600 and 1633 cm−1 (phenylpropanoids); 1547 cm−1 (shifted from 1523 cm−1 in healthy) species (carotenoids) Fusarium infection is associated with degradation of phenylpropanoids and deposition of protein in maize kernels; pathogen converts monomeric sugars polymeric carbohydrates
 Maize, grain Aspergillus flavus [16] Handheld spectrometer (λ = 1064 nm; P = 200 mW; T = 30 s) 1003–1115 cm−1 (monomeric sugars); 1600–1633 (phenylpropanoids) 1600 and 1633 cm−1 (phenylpropanoids); 1547 cm−1 (shifted from 1523 cm−1 in healthy) species (carotenoids); 1153 cm−1 (starch) A. flavus is associated with a breakdown maize starch into monomeric sugars
 Maize, grain A. niger [16] Handheld spectrometer (λ = 1064 nm; P = 200 mW; T = 30 s) 1153 cm−1 (starch); 1600–1633 (phenylpropanoids) 1600 and 1633 cm−1 (phenylpropanoids); 1547 cm−1 (shifted from 1523 cm−1 in healthy) species (carotenoids) A. niger converts monomeric sugars polymeric carbohydrates
 Maize, grain Diplodia spp. [16] Handheld spectrometer (λ = 1064 nm; P = 200 mW; T = 30 s) 1003–1115 cm−1 (monomeric sugars) 1153 cm−1 (starch) Diplodia is associated with a breakdown maize starch into monomeric sugars
 Abutilon hybridum, leaf Abutilon mosaic virus [29] Handheld spectrometer (λ = 1064 nm; P = 200 mW; T = 8 s) 1605–1629 (phenylpropanoids); 1440–1460 cm−1 (aliphatic) Abutilon mosaic virus is associated with an increase in phenylpropanoids in Abutilon hybridum
 Tomatoes, leaf Tomato yellow leaf curl Sardinia virus (TYCLSV) [45] Benchtop spectrometer (λ = 780 nm; P = 2mW; T = 5–10 s) 1608 cm−1 (phenolic); 1483 cm−1 (aliphatic) 1526 cm−1 (carotenoids); 1420, 1483 cm−1 (aliphatic), 1500, 1608 cm−1 (phenolic); 1353 cm−1 (unidentified); Small changes in plant biochemistry
 Tomatoes, leaf Tomato spotted wilt virus (TSWV) [45] Benchtop spectrometer (λ = 780 nm; P = 2mW; T = 5–10 s) 1608 cm−1 (phenolic); 1438 cm−1 (aliphatic); 1353 cm−1 (unidentified); 1483 cm−1 (aliphatic) Small changes in plant biochemistry
 Wheat, leaf Barley yellow dwarf virus (BYDV) [36] Handheld spectrometer (λ = 830 nm; P = 495 mW; T = 1 s) 1601–1630 cm−1 (phenylpropanoids) 1000, 1115, 1156, 1186, 1218 and 1525 cm−1 (carotenoids) BYDV is associated with an increase in phenylpropanoids and decrease in carotenoids
 Wheat, leaf Wheat streak mosaic virus (WSMV) [36] Handheld spectrometer (λ = 830 nm; P = 495 mW; T = 1 s) 1601–1630 cm−1 (phenylpropanoids) 1000, 1115, 1156, 1186 and 1218 cm−1 (carotenoids) WSMV is associated with an increase in phenylpropanoids and decrease in carotenoids
 Potato, tubers Zebra chip [112] Handheld spectrometer (λ = 830 nm; P = 495 mW; T = 1 s) 1153 (carbohydrates) Zebra chip is associated with degradation of carbohydrates in tubers
 Potato, tubers Virus Y [112] Handheld spectrometer (λ = 830 nm; P = 495 mW; T = 1 s) 1153 cm−1 (carbohydrates) Virus Y is associated with an increase in carbohydrates in tubers
Abiotic stresses
 Coleus lime (Plectranthus scutellarioides), leaves Saline, light, drought and cold [26] Benchtop spectrometer (λ = 532 nm; P = 10 mW; T = 10 s) 620 and 740 cm−1 (anthocyanins) 1000 and 1170 cm−1 (carotenoids) Saline, light, drought and cold stresses cause an increase in anthocyanins and a decrease in carotenoids
 Arabidopsis thaliana, leaves Nitrogen deficiency [10] Postable spectrometer (λ = 830 nm; P = 100 mW; T = 10 s) 1064 cm−1 (nitrate) 1046 cm–1 peak intensity correlates with the nitrate content in Arabidopsis plants
 Rice, leaves Nitrogen deficiency [8] Handheld spectrometer (λ = 830 nm; P = 495 mW; T = 1 s) 1600–1630 cm−1 (phenylpropanoids) 1115–1218 cm−1 (carotenoids) Nitrogen deficiency is associated with a decrease in carotenoids and increase in phenylpropanoids
 Rice, leaves Phosphorus and potassium deficiencies [8] Handheld spectrometer λ = 830 nm; P = 495 mW; T = 1 s) Small changes in 1600–1630 cm−1 (phenylpropanoids) Small changes in 1115–1218 cm−1 (carotenoids) Phosphorus and potassium deficiencies are associated with a decrease in carotenoids and increase in phenylpropanoids
Identification of plant species and their varieties; nutritional analysis
 Poison ivy, leaves Farber et al. [36] Handheld spectrometer (λ = 830 nm; P = 495 mW; T = 1 s) 1717 cm−1 (carboxyl or ester groups) 1717 cm−1 band can be used to identify poison ivy
 Peanuts, leaves and seeds Farber et al. [36] Handheld spectrometer (λ = 830 nm; P = 495 mW; T = 1 s)

Identification: all bands

Nutritional analysis: 1005 cm−1 (proteins), 1301 cm−1 (carbohydrates), 1443 cm−1 (oils), 1606 cm−1 (fiber), 1656 cm−1 (unsaturated fatty acids), and 1748 cm−1 (esters)

Identification of peanut varieties can be achieved though spectroscopic analysis of leaves and seeds with 80% and 95% accuracy, respectively. RS can be used to predict relative concentration of proteins, carbohydrates, oils, fiber, unsaturated fatty acids and esters in peanut seeds
 Potato, tubers Morey et al. [34] Handheld spectrometer (λ = 830 nm; P = 495 mW; T = 1 s)

Identification: all bands

Nutritional analysis: 1126 cm−1 (starch), 1527 cm−1 (carotenoids), 1600 cm−1 (phenylpropanoids), 1660 cm−1 (proteins)

Identification of potato varieties can be achieved though spectroscopic analysis of tubers with 77.5% accuracy. RS can be used to predict relative concentration of proteins, carotenoids, starch and phenylpropanoids in potato tubers
 Corn, kernels Krimmer et al. [21] Handheld spectrometer (λ = 830 nm; P = 495 mW; T = 1 s)

Identification: all bands

Nutritional analysis: 479 cm−1 (starch), 1527 cm−1 (carotenoids), 1600/1632 cm−1 (phenylpropanoids), 1000/1660 cm−1 (proteins)

Identification of corn varieties can be achieved though spectroscopic analysis of kernels with 95% accuracy. RS can be used to predict relative concentration of proteins, carotenoids, and starch in corn kernels
 Citrus, fruits Feng et al. [74] Benchtop spectrometer (λ = 514 nm; P = 20 mW; T = 10 s) All bands RS can be used to identify citrus fruits
 Loquat, fruits Zhu et al. [47] Benchtop spectrometer (λ = 532 nm; P = 25 mW; T = 1 s) 1602 cm−1 (lignin) RS can be used to determine fruit ripening
 Tomatoes, fruits Martin et al. [77] Benchtop spectrometer (λ = 532 nm; P = 46–50 mW; T = 10 s) 1150, 1257 cm−1 (carotenoids) RS can be used to predict tomato ripeness
 Mandarin oranges, fruits Nekvapil et al. [79] Benchtop spectrometer (λ = 532 nm; P = 200 mW; T = 10 s) 1100–1250, 1527 cm−1 (carotenoids) RS can be used to predict fruit freshness
 Wheat, grain Piot et al. [80] Benchtop spectrometer (λ = ’red light’; P = 8 mW) 471–485 cm−1 (starch), 1065–1140 cm−1 (lipids), 1630–1670 cm−1 (protein) RS can be used to probe concentration of starch, lipids and proteins in the grain
 Coffee, beans Keidel et al. [81] Benchtop spectrometer (λ = 1064 nm; P = 300 mW)

Identification: all bands

Kahweol concentration: 1479 and 1567 cm−1

RS can be used to predict the geographical origins of coffee beans
 Hemp and cannabis Sanchez et al. [8] Handheld spectrometer (λ = 830 nm; P = 495 mW; T = 1 s)

Identification: all bands

Cannabinoid content: 780, 1295, 1623, and 1666 cm−1

RS can be used to identify cannabis varieties and determine concentrations of cannabinoids in the plant