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Article

The Volatile Phytochemistry of Seven Native American Aromatic Medicinal Plants

by
Sims K. Lawson
1,
Prabodh Satyal
2 and
William N. Setzer
2,3,*
1
Penn State College of Agricultural Sciences, Department of Ecosystem Science and Management, 117 Forest Resources Building, University Park, PA 16802, USA
2
Aromatic Plant Research Center, Suite 100, Lehi, UT 84043, USA
3
Department of Chemistry, University of Alabama in Huntsville, Huntsville, AL 35899, USA
*
Author to whom correspondence should be addressed.
Plants 2021, 10(6), 1061; https://doi.org/10.3390/plants10061061
Submission received: 4 May 2021 / Revised: 23 May 2021 / Accepted: 23 May 2021 / Published: 25 May 2021
(This article belongs to the Special Issue Phytochemistry of Aromatic and Medicinal Plants)
Browse Figure
Versions Notes

Abstract

:
As part of our evaluation of essential oils derived from Native American medicinal plants, we have obtained the essential oils of Agastache foeniculum (Pursch) Kuntze (Lamiaceae), Gaultheria procumbens L. (Ericaceae), Heliopsis helianthoides (L.) Sweet (Asteraceae), Liatris spicata (L.) Willd. (Asteraceae), Pycnanthemum incanum (L.) Michx. (Lamiaceae), Smallanthus uvedalia (L.) Mack. ex Mack. (Asteraceae), and Verbena hastata L. (Verbenaceae) by hydrodistillation. The essential oils were analyzed by gas chromatographic techniques. The essential oil of A. foeniculum was dominated by estragole (88–93%), while methyl salicylate (91%) dominated the G. procumbens essential oil. Germacrene D was the major component in H. helianthoides (42%) and L. spicata (24%). 1,8-Cineole (31%) and α-terpineol (17%) were the main compounds in P. incanum essential oil. The essential oil of S. uvedalia showed α-pinene (24%), perillene (15%), and β-caryophyllene (17%) as major components. Verbena hastata essential oil was rich in 1-octen-3-ol (up to 29%) and palmitic acid (up to 22%). Four of these essential oils, H. helianthoides, L. spicata, P. incanum, and V. hastata, are reported for the first time. Additionally, the enantiomeric distributions of several terpenoid components have been determined.

Graphical Abstract

1. Introduction

Plants have been used in traditional medicine since prehistoric times. The therapeutic properties of medicinal plants are generally attributed to secondary metabolites produced by the plants as protection against pathogens and herbivory. As with many other aboriginal peoples, Native North Americans have used plants as medicines throughout their history. Although not as extensively documented as traditional Chinese medicine or Ayurvedic medicine, there are several sources of information regarding Native American ethnopharmacology [1,2,3]. As part of our ongoing investigations of the essential oil compositions of Native American medicinal plants, we have collected and examined seven aromatic medicinal plants growing in the southeastern United States.
Agastache foeniculum (Pursch) Kuntze (Lamiaceae) is native to north central United States and southern Canada, but has been recorded in southern Alabama [4]. The plant has been introduced to Europe, particularly the U.K., the Netherlands, and Germany, as an ornamental [5]. Cheyenne and Chippewa Native Americans used an infusion of the leaves of A. foeniculum as a cold medicine [2]. Essential oil compositions of A. foeniculum have been extensively studied, and the oils are typically dominated by methyl chavicol (estragole) with smaller amounts of (E)-anethole [6]. Nonvolatile phytochemicals from A. foeniculum include flavonoids (apigenin, quercetin), polyphenolics (rosmarinic acid, caffeic acid), pentacyclic triterpenoids (α-amyrin, β-amyrin), and sterols (campesterol, campestanol, sitosterol, stigmasterol, stigmastanol) [6].
Gaultheria procumbens L. (Ericaceae) naturally ranges in eastern North America from Canada, south through Alabama and Georgia [4]. Several native North American tribes used an infusion of G. procumbens to treat headaches, colds (Algonquin, Cherokee, Chippewa, Iroquois) or to treat arthritis, rheumatism, and lumbago (Iroquois, Menominee, Ojibwa, Potawatomi) [2]. The Cherokee were known to use a root infusion of G. procumbens along with the roots of Epigaea repens for chronic indigestion, and they also chewed the leaves as a substitute for chewing tobacco [7]. Much like its Asian relative, Gaultheria fragrantissima Wall., the essential oil of G. procumbens is dominated by methyl salicylate. Commercial G. fragrantissima essential oil (doTERRA International, Pleasant Grove, Utah) has 99.7% methyl salicylate, while methyl salicylate in G. procumbens essential oil typically ranges 96.6–99.8% [8,9,10].
Heliopsis helianthoides (L.) Sweet (Asteraceae) is native to North America from Saskatchewan, Canada east to the Atlantic coast of Newfoundland and south to the Gulf of Mexico, with the western range extending as far as New Mexico [4,11,12]. There are three subspecies of H. helianthoides, ssp. helianthoides, generally occurring east of the Mississippi River; ssp. occidentalis, found in the Great Plains region; and ssp. scabra, which is predominant in the Ozark region (Missouri, Arkansas, and Oklahoma) [11]. The Chippewa took a decoction of the roots of H. helianthoides as a stimulant [2]. The Cherokee used the roots in combination with Scutellaria incana “for young women”, presumably for menstruation-related discomforts, and sore feet were relieved by soaking in an infusion of what was called “swamp sunflower” [7]. Guaianolide sesquiterpenoids [13], N-alkylamides [14], and lignans [15] have been isolated and characterized from H. helianthoides.
The natural range of Liatris spicata (L.) Willd. (Asteraceae) is the eastern United States and Canada, east of the Mississippi River, from the south along the Gulf of Mexico including southern Alabama and northern Florida areas, north to Ontario and Quebec [4,16,17]. The Cherokee used the plant as an analgesic for backache and limb pains [2]. The guaianolide sesquiterpenoid spicatin has been isolated from the chloroform extract of L. spicata [18].
Pycnanthemum incanum (L.) Michx. (Lamiaceae) ranges naturally in the eastern United States from the Mississippi River east to the Atlantic coast and from southern Ontario, Canada south to the Gulf of Mexico, though it is primarily found from the Appalachian mountain region beginning in north Georgia north into Ontario, Canada [4,19]. The Cherokee and Choctaw people used the leaves of P. incanum externally to treat headaches [2]. Dein and Munafo have characterized the key odorants from P. incanum to be β-ionone, myrcene, linalool, and pulegone [20].
The natural range of Smallanthus uvedalia (L.) Mack. ex Mack. (Asteraceae) is the southeastern United States, from the Ohio river basin south to the Gulf of Mexico [4]. Smallanthus uvedalia was reportedly used internally by Native American Indians for laxative properties as well as a stimulant and also to treat swollen glands, especially mastitis [21]. The Cherokee used a salve of the roots to treat burns and cuts, while the Iroquois took an infusion of the plant for back pain and as an antiemetic [2]. Interestingly, the Cherokee were also reported to have used a tea made from this plant to induce vomiting, though it is unclear which portion was used [7]. A number of germacranolide sesquiterpenoids and ent-kaurane diterpenoids have been isolated and characterized from S. uvedalia [22]. The leaf essential oils of S. uvedalia from several locations in north Alabama have been analyzed previously [23,24].
Verbena hastata L. (Verbenaceae) ranges throughout North America [4]. The Cherokee used the plant to treat colds and coughs and to alleviate fevers [2]. The ethanol leaf extract of V. hastata has shown antiplasmodial [25], antinociceptive, anti-inflammatory, antipyretic [26], and anti-ulcer activities [27]. The iridoid glycoside hastatoside has been isolated from V. hastata [28].
The purpose of this study was to extend our understanding of the volatile phytochemistry of Native American aromatic medicinal plants by examination of the essential oils of these seven plant species, to determine their chemical compositions as well as the enantiomeric distributions of terpenoid constituents.

2. Results and Discussion

The essential oils of each species were obtained by hydrodistillation of dried plant material (Table 1).

2.1. Agastache foeniculum (Pursch) Kuntze (Lamiaceae)

The aerial parts of three different plant samples of A. foeniculum were collected from cultivated plants in Newville, Alabama. Hydrodistillation gave pale yellow essential oils in yields ranging from 1.48% to 2.30% yield. The essential oil compositions are compiled in Table 2.
The A. foeniculum essential oil was dominated by the phenylpropanoid methyl chavicol (=estragole). There are apparently five different chemotypes of A. foeniculum based on essential oil chemical profiles: (1) methyl chavicol, (2) spathulenol/bornyl acetate, (3) γ-cadinene/α-cadinol, (4) limonene, and (5) isomenthone [33,34]. Most A. foeniculum essential oils belong to the methyl chavicol chemotype, however [33,35,36,37,38,39,40,41,42].
Methyl chavicol contributes to the anise-like aroma of A. foeniculum and has shown anti-inflammatory and anti-edematogenic [43,44], cytotoxic [45], and antimicrobial activities against phytopathogens [46,47]. Unfortunately, however, methyl chavicol has also shown genotoxic and carcinogenic activities [48,49].

2.2. Gaultheria procumbens L. (Ericaceae)

The leaf essential oil of G. procumbens was obtained in 4.25% yield and the major component was methyl salicylate (91.1%) (Table 3). Methyl salicylate is the dominating component in G. procumbens essential oil regardless of geographical location of cultivation, ranging in concentration from 61.14% to 99.96% [8,9,10,50,51,52].
The major component of G. procumbens essential oil, methyl salicylate, is well-known as an anti-inflammatory, antipyretic, analgesic agent [53], and accounts for the traditional use of the herb by Native Americans. Methyl salicylate is a common flavoring and fragrance ingredient in cosmetics, shampoos, toilet soaps, and other toiletries, however, it is also a potentially hazardous intoxicant [54,55,56].

2.3. Heliopsis helianthoides (L.) Sweet (Asteraceae)

The essential oil from the aerial parts of H. helianthoides was obtained in 0.95% yield. The major component in the essential oil was germacrene D (42.4%), with a lesser amount of 4-vinylguaicol (5.5%) (Table 4). As far as we are aware, this is the first report on the chemical composition of H. helianthoides essential oil.
Although not necessarily a phytochemical marker of the family, germacrene D has been found to be a major component in several members of the Asteraceae. For example, germacrene D is the dominant compound in the essential oils of Centaurea hadimensis Wagenitz, K. Ertugrul & H. Dural (44.3%) [57], Centaurea pseudoscabiosa Boiss. & Buhse (36.0%) [57], Eupatorium cannabinum L. (33.5%) [58], Polymnia canadensis L. (63.6%) [23], Rudbeckia fulgida Aiton (30.1%) [59], Rudbeckia hirta L. (23.6%) [59], Solidago canadensis L. (64.1%) [60], Symphyotrichum novae-angliae (L.) G.L. Nesom (25.5%) [59], Verbesina macrophylla (Cass.) F.S. Blake (37.3%) [61], Verbesina turbacensis Kunth (36.9%) [62], and Liatris spicata (23.7%, this work, see below). Germacrene D has shown antimicrobial and cytotoxic activities [63,64].

2.4. Liatris spicata (L.) Willd. (Asteraceae)

The essential oil composition of L. spicata essential oil is presented in Table 5. The major components were germacrene D (23.7%), myrcene (13.7%), α-pinene (8.1%), and caryophyllene oxide (5.9%). Apparently, there have been no previous reports on the essential oil composition of L. spicata.

2.5. Pycnanthemum incanum (L.) Michx. (Lamiaceae)

Table 6 shows the chemical composition of the essential oil from the aerial parts of P. incanum growing wild in South Carolina. The essential oil was rich in oxygenated monoterpenoids, including 1,8-cineole (30.7%), α-terpineol (16.9%), borneol (8.2%), and cis-sabinene hydrate (5.6%). The sesquiterpene hydrocarbons (E)-β-caryophyllene (11.0%), and germacrene D (5.0%) were also relatively abundant. To our knowledge, this is the first reported analysis of P. incanum essential oil. Volatiles obtained from a diethyl ether extract have been analyzed by gas chromatography-olfactometry to determine the key odorants [20]. Although the percentages of the volatiles were not reported, the enantiomeric distributions of several components were determined (Table 6). 1-Octen-3-ol, isomenthone, α-terpineol, and pulegone showed comparable enantiomeric distributions between P. incanum essential oil and the volatiles from the previously published diethyl ether extract [20]. Concentrations of α-pinene, linalool, and menthol were too low in this current study to obtain reliable enantiomeric distributions for comparison.

2.6. Smallanthus uvedalia (L.) Mack. ex Mack. (Asteraceae)

The essential oil composition of S. uvedalia from South Carolina is summarized in Table 7. The major components of S. uvedalia essential oil were α-pinene (23.9%), (E)-β-caryophyllene (16.9%), perillene (14.5%), germacrene D (12.2%), and limonene (6.1%). In comparison, S. uvedalia from northern Alabama (collected in September 2018) contained α-pinene (62.6%), limonene (11.4%), and β-pinene (6.0%), with lesser concentrations of (E)-β-caryophyllene (3.8%) [24]. Neither perillene nor germacrene D were observed in this northern Alabama sample. In contrast, two S. uvedalia samples collected in February, 2016, from northern Alabama were rich in (E)-β-caryophyllene (24.5% and 16.5%) and caryophyllene oxide (19.8% and 14.2%) [23]. α-Pinene concentrations were low (1.3% and 0.0%) and neither perillene nor germacrene D were observed. The differences in compositions in S. uvedalia may be attributed to geographical location and/or seasonal variation.
There does not seem to be a trend in the major enantiomers for essential oils of the Asteraceae (see Supplementary Table S1). For example, (+)-α-pinene was the only enantiomer observed in Erechtites hieracifolia (L.) Raf. [65], but (–)-α-pinene predominated in S. uvedalia (this work). Likewise, (+)-β-pinene was the only enantiomer in Coreopsis capillacea Kunth (syn. C. triloba S.F. Blake) [66], while (–)-β-pinene was the dominant enantiomer in Achillea ligustica All. [67]. (+)-Limonene was the dominant enantiomer in S. uvedalia (this work) and Solidago canadensis L. [68], whereas the (–)-enantiomer dominated E. hieracifolia [65] and C. capillacea [66].

2.7. Verbena hastata L. (Verbenaceae)

Three different specimens of V. hastata were collected and investigated (Table 8). Although collected from the same general location on the same day, the essential oils showed notable quantitative differences in their compositions. For example, the concentration of 1-octen-3-ol ranged from 2.4% to 29.1%, nonanal ranged from 1.8% to 11.1%, palmitic acid 8.5–21.6%, 1-octadecanol 2.8–14.0%, and phytol 5.2–12.6%. The enantiomeric distributions of linalool, α-terpineol, (E)-β-ionone, and (E)-nerolidol were the same for the three samples, however. As far as we know, this is the first report on the essential oil composition of V. hastata.
There are few Verbena essential oil compositions to compare. However, several Verbena officinalis L. essential oils have been reported, and these samples also show wide variation in composition. The major components in V. officinalis essential oil from Morocco were spathulenol (10.8%), limonene (7.5%), 1,8-cineole (7.5%), caryophyllene oxide (7.3%), and ar-curcumene (6.0%) [69]. In contrast, the essential oil of V. officinalis from Italy was rich in geranial (45.5%) and isobornyl formate (41.4%) [70]. Verbena officinalis from Algeria, on the other hand, showed limonene (17.7%), geranial (14.8%), carvone (14.2%), and caryophyllene oxide (12.4%) as major components [71].
The (–)-enantiomer of 1-octen-3-ol was the only stereoisomer observed in V. hastata essential oils as it was in P. incanum essential oil (above). Notably, (–)-1-octen-3-ol is the major enantiomer, generally greater than 97%, in mushrooms [72], and is the stereoisomer responsible for mushroom odor [73]. Interestingly, although both enantiomers and the racemic mixture of 1-octen-3-ol attract mosquitoes, the (–)-enantiomer attracted more mosquito species [74].
A racemic mixture was observed for α-terpineol, but there was a higher concentration of (–)-linalool over (+)-linalool in V. hastata. (–)-Linalool also dominated in the essential oil of Lantana camara L. (Verbenaceae) from Madagascar [75]. In contrast, linalool in the essential oil of Lippia alba (Mill.) N.E. Brown (Verbenaceae) from Uruguay was dominated by the (+)-enantiomer [76].

3. Materials and Methods

3.1. Plant Material

The aerial parts of A. foeniculum, G. procumbens, and H. helianthoides were obtained from plants cultivated in at Kirkland Gardens, in Newville, Alabama (Table 1). The cultivated plants were started from commercially available seeds (A. foeniculum, Homegrown Seed Company, and H. helianthioides, Prairie Moon Nursery), tubers (L. spicata, Wal-Mart), or young plants (G. procumbens, The Home Depot). All the plants were grown in full sun, except the G. procumbens, which was located in a partially shaded location (4 h/day average sunlight), and all were watered at least once a week. The plants were cultivated directly in the ground, which was clayey-loamy sand, which was amended with composted chicken manure, worm castings, kelp meal, and bone meal at time of planting. Pycnanthemum incanum and S. uvedalia were collected in the wild from a fully shaded forest understory roadside location near a small waterfall in northern South Carolina. The plants were located beside highway 276 near the North Carolina–South Carolina border (see Table 1). The soil was a thick loam with a lot of leaf litter. Verbena hastata was collected in the wild near a disturbed fence-line area with full sun between a bovine field and a paved county road in rural Newville, Alabama (Table 1). Specimens of each plant were collected during the flowering phase (Table 1). Voucher specimens of P. incanum (SKL83120), S. uvedalia (SKL31820), and V. hastata (SKL51321) were deposited in the University of Alabama in Huntsville Herbarium (HALA); cultivated plants were not vouchered. For each species, the plant material was air-dried in the laboratory (around 23 °C) for 10 days. The dried plant materials of each species were chopped and hydrodistilled using a Likens–Nickerson apparatus with continuous extraction with dichloromethane for 4 h. The dichloromethane was evaporated using a stream of dry nitrogen to give the essential oils (Table 1).

3.2. Gas Chromatographic Analysis

The essential oils were analyzed by gas chromatography-mass spectrometry (GC-MS), gas chromatography-flame ionization detection (GC-FID), and chiral GC-MS as previously described [77].
GC-MS: Shimadzu GCMS-QP2010 Ultra, electron impact (EI) mode (electron energy = 70 eV), scan range = 40–400 atomic mass units, scan rate = 3.0 scans/s, and GC-MS solution software; ZB-5ms fused silica capillary column (30 m length × 0.25 mm inner diameter) with a (5% phenyl)-polymethylsiloxane stationary phase and a film thickness of 0.25 μm; He carrier gas with a column head pressure of 552 kPa and flow rate of 1.37 mL/min; injector temperature = 250 °C, ion source temperature = 200 °C; GC oven temperature 50–260 °C (2 °C/min), 1-μL injection of 5% solution of EO in dichloromethane (split mode, 30:1). The essential oil components were identified by MS fragmentation, and retention indices compared with those in the databases [29,30,31,32].
GC-FID: Shimadzu GC 2010 equipped with flame ionization detector, a split/splitless injector, and Shimadzu autosampler AOC-20i, with a ZB-5 capillary column (30 m length × 0.25 mm inner diameter) with a (5% phenyl)-polymethylsiloxane stationary phase and a film thickness of 0.25 μm; oven temperature was programmed the same as above for GC-MS; injector temperature = 250 °C, detector temperature = 280 °C, N2 carrier gas, and flow rate = 1.0 mL/min. The composition percentages were calculated from raw peak areas without standardization.
Chiral GC-MS: Shimadzu GCMS-QP2010S, EI mode (electron energy = 70 eV) with scan range of 40–400 amu and scan rate of 3.0 scans/s; Restek B-Dex 325 capillary column (30 m × 0.25 mm ID × 0.25 μm film); GC oven temperature program, 50–120 °C (1.5 °C/min), 120–200 °C (2 °C/min), and kept at 200 °C for 5 min; He carrier gas, flow rate = 1.8 mL/min; 0.1-μL injection of 3% solution of EO in dichloromethane (split mode, 1:45). The monoterpenoid enantiomers were identified by comparison of retention times with authentic samples obtained from Sigma-Aldrich (Milwaukee, WI, USA). Relative enantiomer percentages were determined based on peak areas. Chiral GC-MS chromatograms are available as Supplementary Figures S1–S7.

4. Conclusions

This report presented the essential oil compositions of seven aromatic medicinal plants used by Native Americans. Four of these essential oils, Heliopsis helianthoides, Liatris spicata, Pycnanthemum incanum, and Verbena hastata, were reported for the first time. Additionally, the enantiomeric distributions of several terpenoid components have been determined. The chemical compositions presented add to our knowledge of the phytochemistry of the medicinal plants.

Supplementary Materials

The following are available online at https://www.mdpi.com/article/10.3390/plants10061061/s1, Table S1: Enantiomeric distribution of terpenoids in Asteraceae species, Figure S1: Chiral gas chromatogram of Agastache foeniculum essential oil, Figure S2: Chiral gas chromatogram of Gaultheria procumbens essential oil, Figure S3: Chiral gas chromatogram of Helianthus helianthoides essential oil, Figure S4: Chiral gas chromatogram of Liatris spicata essential oil, Figure S5: Chiral gas chromatogram of Pycnanthemum incanum essential oil, Figure S6: Chiral gas chromatogram of Smallanthus uvedalia essential oil, Figure S7: Chiral gas chromatogram of Verbena hastata essential oil.

Author Contributions

Conceptualization, S.K.L. and W.N.S.; methodology, S.K.L., P.S. and W.N.S.; software, P.S.; validation, W.N.S.; formal analysis, P.S. and W.N.S.; investigation, S.K.L., P.S. and W.N.S.; data curation, W.N.S.; writing—original draft preparation, W.N.S.; writing—review and editing, S.K.L., P.S. and W.N.S. All authors have read and agreed to the published version of the manuscript.

Funding

This research received no external funding.

Data Availability Statement

All data are presented in this report.

Acknowledgments

This work was carried out as part of the activities of the Aromatic Plant Research Center (APRC, https://aromaticplant.org/) (accessed on 23 May 2021).

Conflicts of Interest

The authors declare no conflict of interests.

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Table
Table 1. Collection and hydrodistillation details of seven Native American medicinal plants a.
Table 1. Collection and hydrodistillation details of seven Native American medicinal plants a.
Plant SpeciesCollection Site (Date)Mass of Plant MaterialEssential Oil Yield
Agastache foeniculum #1Cultivated, Kirkland Gardens, 31° 26″ 27′ N, 85° 21″ 31′ W (5 May 2020)24.78 g dried aerial parts367.1 mg (1.48%) pale yellow essential oil
Agastache foeniculum #2Cultivated, Kirkland Gardens, 31° 26″ 27′ N, 85° 21″ 31′ W (5 May 2020)28.22 g dried aerial parts587.7 mg (2.08%) pale yellow essential oil
Agastache foeniculum #3Cultivated, Kirkland Gardens, 31° 26″ 27′ N, 85° 21″ 31′ W (5 May 2020)13.77 g dried aerial parts316.6 mg (2.30%) pale yellow essential oil
Gaultheria procumbensCultivated, Kirkland Gardens, 31° 26″ 27′ N, 85° 21″ 31′ W (10 June 2020)3.01 g dried leaves127.8 mg (4.25%) pale yellow essential oil
Heliopsis helianthoidesCultivated, Kirkland Gardens, 31° 26″ 27′ N, 85° 21″ 31′ W (24 July 2020)27.70 g dried aerial parts263.6 mg (0.95%) pale yellow essential oil
Liatris spicataCultivated, Kirkland Gardens, 31° 26″ 27′ N, 85° 21″ 31′ W (24 July 2020)31.90 g dried aerial parts133.1 mg (0.420%) pale yellow essential oil
Pycnanthemum incanumWild-growing, South Carolina, 35° 06’ 08.1″ N, 82° 36’ 44.4″ W (31 August 2020)9.82 g dried aerial parts168.1 mg (1.71%) pale yellow essential oil
Smallanthus uvedaliaWild-growing, South Carolina, 35° 06’ 08.1″ N, 82° 36’ 44.4″ W (31 August 2020)90.77 g dried aerial parts369.7 mg (0.41%) yellow essential oil
Verbena hastata #1Wild-growing, Newville, Alabama, 31° 26″ 27′ N, 85° 21″ 31′ W (25 May 2020)24.61 g dried aerial parts134.2 mg (0.55%) pale yellow essential oil
Verbena hastata #2Wild-growing, Newville, Alabama, 31° 26″ 27′ N, 85° 21″ 31′ W (25 May 2020)28.50 g dried aerial parts62.2 mg (0.22%) pale yellow essential oil
Verbena hastata #3Wild-growing, Newville, Alabama, 31° 26″ 27′ N, 85° 21″ 31′ W (25 May 2020)36.22 g dried aerial parts214.2 mg (0.59%) pale yellow essential oil
a The volatile materials reported in this research were obtained by hydrodistillation with continuous solvent extraction using a Likens–Nickerson apparatus. Many researchers consider these products not to be true “essential oils”, but rather “volatile fractions”.
Table
Table 2. Essential oil composition of three samples of anise fennel (Agastache foeniculum) cultivated in south Alabama.
Table 2. Essential oil composition of three samples of anise fennel (Agastache foeniculum) cultivated in south Alabama.
RIcalcRIdbCompoundPercent Composition
#1#2#3
924927α-Thujenetrtr---
932933α-Pinenetrtrtr
963964Benzaldehydetr0.10.1
971972Sabinenetrtrtr
971974Hexanoic acid------tr
9759741-Octen-3-ol0.30.70.6
9839843-Octanone0.10.20.2
987989Myrcene0.10.1tr
10161018α-Terpinene0.1------
10241024p-Cymene0.6tr---
10281030Limonene1.54.92.9
10301033Benzyl alcohol---0.10.1
10301031β-Phellandrenetrtrtr
103210321,8-Cineoletr------
10571057γ-Terpinene0.1------
10661068Acetophenonetr------
10691069cis-Sabinene hydratetr------
10971099Linalool0.1trtr
110411071-Octen-3-yl acetate0.10.20.1
11981197Methyl chavicol (=Estragole)93.288.491.5
12131217Coumaran---trtr
12481250Chavicol0.10.20.3
12821285(E)-Anethole---trtr
12871289Thymol0.90.10.1
12951296Carvacrol0.1trtr
130913094-Vinylguaiacol---trtr
13331334Bicycloelemene---trtr
13551356Eugenol0.10.10.2
13621362Chavibetol0.72.30.7
13791379(E)-β-Damascenone---trtr
13841382β-Bourbonene---trtr
13901390trans-β-Elemene---trtr
13921392(Z)-Jasmone---tr0.1
14011403Methyl eugenoltr0.1tr
14171417(E)-β-Caryophyllene1.21.61.9
14521453α-Humulenetr0.10.1
14751475γ-Muurolene---trtr
14781481(E)-β-Ionone---trtr
14811483Germacrene D0.20.30.2
14871487β-Selinene---tr---
14911491Viridiflorene---trtr
14961497Bicyclogermacrene0.40.40.6
15041503(E,E)-α-Farnesene---trtr
15131512γ-Cadinene---trtr
15181518δ-Cadinenetr0.10.1
15751574Germacrene D-4-ol0.10.10.2
15761577Caryophyllene oxide---trtr
15851590Globulol---trtr
15931594Viridiflorol---trtr
16411643τ-Cadinol---trtr
16411644α-Muurolol (=δ-Cadinol)------tr
16431644τ-Muurolol---trtr
16561655α-Cadinol0.10.10.1
Monoterpene hydrocarbons2.44.92.9
Oxygenated monoterpenoids1.00.10.1
Sesquiterpene hydrocarbons1.82.52.8
Oxygenated sesquiterpenoids0.20.20.3
Benzenoid aromatics94.191.392.9
Others0.51.00.9
Total identified100.0100.0100.0
CompoundEnantiomeric Distribution (+):(-)
#1#2#3
Sabinene---100:0100:0
1-Octen-3-ol0:1000:1000:100
Limonene98.2:1.898.3:1.798.3:1.7
β-Phellandrene100:0100:0100:0
Linalool29.3:70.729.5:70.521.3:78.7
trans-β-Elemene---60.4:39.657.9:42.1
(E)-β-Caryophyllene100:0100:0100:0
Germacrene D100:0100:0100:0
δ-Cadinene0:1000:1000:100
RIcalc = retention indices calculated with respect to a homologous series of n-alkanes on a ZB-5 column. RIdb = retention indices from the databases [29,30,31,32]. tr = trace (<0.05%).
Table
Table 3. Essential oil composition of American wintergreen (Gaultheria procumbens) cultivated in southern Alabama.
Table 3. Essential oil composition of American wintergreen (Gaultheria procumbens) cultivated in southern Alabama.
RIcalcRIdbCompound%
10331033Benzyl alcohol0.2
105110512,3,6-Trimethylhepta-1,5-dienetr
11051104Nonanaltr
11601158Menthone0.1
11931192Methyl salicylate91.1
12151217Coumarantr
12371237Pulegone0.6
12621263(2E)-Decenaltr
12711273(E)-Cinnamaldehydetr
12891289Thymol0.3
13041304(E)-Cinnamyl alcohol0.8
13361339Piperitenonetr
13881390trans-β-Elemenetr
14171417(E)-β-Caryophyllenetr
14311432trans-α-Bergamotenetr
14451447Geranyl acetone0.1
14671463Tuberolactone5.3
14701471Massoia lactone1.3
14791480Germacrene D0.1
15021503(E,E)-α-Farnesenetr
15161518δ-Cadinenetr
15791577Caryophyllene oxidetr
16521655α-Cadinoltr
167916768-Hydroxyisobornyl isobutanoatetr
17611762Benzyl benzoatetr
18631869Benzyl salicylatetr
Monoterpene hydrocarbonstr
Oxygenated monoterpenoids1.1
Sesquiterpene hydrocarbons0.1
Oxygenated sesquiterpenoidstr
Benzenoid aromatics92.1
Others6.6
Total identified99.9
Enantiomeric Distribution(+):(-)
Menthone0:100
Pulegone100:0
(E)-β-Caryophyllene100:0
Germacrene D100:0
RIcalc = retention indices calculated with respect to a homologous series of n-alkanes on a ZB-5 column. RIdb = retention indices from the databases [29,30,31,32]. tr = trace (<0.05%).
Table
Table 4. Essential oil composition of early sunflower (Heliopsis helianthoides) cultivated in southern Alabama.
Table 4. Essential oil composition of early sunflower (Heliopsis helianthoides) cultivated in southern Alabama.
RIcalcRIdbCompoundPercent Composition a
AverageSt. dev.
801801Hexanal1.00.2
8158174-Hydroxy-2-pentanone0.90.3
829831Furfural0.30.1
848850(2E)-Hexenal1.00.2
8798765-Methyl-(3Z)-hexen-2-one0.90.1
959959Benzaldehyde0.30.0
9879892-Pentyl furan0.40.1
11021104Nonanal1.00.0
12901289Thymol1.80.6
12981300Carvacrol1.50.1
130913094-Vinylguaicol5.50.6
13351335δ-Elemene0.50.1
13831382β-Bourbonene2.70.1
13881390trans-β-Elemene0.50.0
14171422β-Ylangene0.90.1
14181417(E)-β-Caryophyllene2.70.0
14281430β-Copaene1.20.1
14431447iso-Germacrene D0.40.0
14541453α-Humulene0.50.0
14771481(E)-β-Ionone0.50.0
14801480Germacrene D42.41.2
14941497Bicyclogermacrene0.80.1
14971502ε-Amorphene0.30.0
15031499(Z)-Dihydroapofarnesal0.30.0
1509---Unidentified b1.10.0
15161518δ-Cadinene0.40.0
15231516(E)-Dihydroapofarnesal0.30.1
15241524Dihydroactinidiolide0.70.0
15571557Germacrene B0.70.0
15601560(E)-Nerolidol0.80.2
156615661,5-Epoxysalvial-4(14)-ene0.30.0
15751576Spathulenol1.20.0
15801577Caryophyllene oxide1.50.0
15901593Salvial-4(14)-en-1-one0.60.0
16261629iso-Spathulenol2.70.0
16381644allo-Aromadendrene epoxide0.30.1
16531655α-Cadinol1.00.1
16831683Germacra-4(15),5,10(14)-trien-1α-ol1.40.2
16851685Eudesma-4(15),7-dien-1β-ol0.50.1
1689---Germacra-4(15),5,10(14)-trien-1β-ol1.10.2
17351735Mint sulfide0.30.1
1763---Unidentified c1.40.0
1827---Unidentified d1.10.0
18401841Phytone1.60.0
20972098γ-Stearolactone2.10.3
21062102Phytol2.81.3
2273---Unidentified e2.30.8
Monoterpene hydrocarbons0.0
Oxygenated monoterpenoids3.3
Sesquiterpene hydrocarbons53.8
Oxygenated sesquiterpenoids12.2
Diterpenoids2.8
Benzenoid aromatics5.8
Others10.6
Total identified88.6
Enantiomeric Distribution(+):(-)
δ-Elemene52.1:47.9
trans-β-Elemene100:0
(E)-β-Caryophyllene100:0
(E)-β-Ionone100:0
Germacrene D89.3:10.7
δ-Cadinene0:100
(E)-Nerolidol0:100
RIcalc = retention indices calculated with respect to a homologous series of n-alkanes on a ZB-5 column. RIdb = retention indices from the databases [29,30,31,32]. a Average of three measurements. b MS(EI): 182(7%), 153(5%), 126(8%), 112(20%), 111(37%), 99(5%), 83(100%), 69(6%), 55(39%), 43(14%), 41(7%). c MS(EI): 236(2%), 193(20%), 180(10%), 175(15%), 165(18%), 147(35%), 137(26%), 123(36%), 121(24%), 109(25%), 105(26%), 95(50%), 93(38%), 81(100%), 79(28%), 69(31%), 55(38%), 43(30%), 41(41%). d MS(EI): 234(11%), 219(11%), 191(91%), 173(19%), 163(48%), 151(71%), 145(41%), 131(37%), 123(100%), 121(42%), 107(55%), 105(40%), 95(42%), 93(59%), 91(75%), 83(72%), 81(81%), 79(66%), 77(57%), 69(48%), 55(75%), 43(52%), 41(100%). e MS(EI): 161(4%), 147(15%), 133(10%), 119(14%), 105(23%), 95(47%), 93(51%), 91(45%), 80(51%), 79(100%), 67(66%), 55(32%), 43(10%), 41(44%).
Table
Table 5. Chemical composition of Liatris spicata aerial parts essential oil.
Table 5. Chemical composition of Liatris spicata aerial parts essential oil.
RIcalcRIdbCompound%ED, (+):(−)
905902Santolinatriene0.5
934932α-Pinene8.117.1:82.9
950950Camphene0.6100:0
973971Sabinene0.9
976974Hexanoic acid0.9
979978β-Pinene3.152.3:47.7
990989Myrcene13.7
10301030Limonene2.133.4:66.6
10321031β-Phellandrene0.4
10471045(E)-β-Ocimene0.5
11001098Perillene0.3
11011099Linalool0.552.9:47.1
11061104Nonanal0.3
11151113(E)-4,8-Dimethylnona-1,3,7-triene0.3
11461145trans-Verbenol0.7
11631164Pinocarvone0.3
11721170Borneol0.70:100
11811180Terpinen-4-ol0.20:100
11961196Myrtenal0.6
12071205Verbenone0.70:100
12841282Bornyl acetate3.00:100
130913094-Vinylguaiacol0.8
13191322(2E,4E)-Decadienal0.4
13231319(3E)-Hexenyl tiglate0.4
13301329Hexyl tiglate0.3
13841382β-Bourbonene0.4
13881387β-Cubebene0.2
13901390trans-β-Elemene1.1
14161414α-Cedrene0.3
14181422β-Ylangene0.4
14191424(E)-β-Caryophyllene4.4100:0
14241423β-Cedrene0.4
14291427γ-Elemene0.7
14331432trans-α-Bergamotene1.8
14471447Geranyl acetone0.3
14531452(E)-β-Farnesene0.3
14551454α-Humulene1.9
14751475γ-Muurolene0.4
14781481(E)-β-Ionone0.2
14811480Germacrene D23.7100:0
14881489β-Selinene0.5
14951497Bicyclogermacrene0.5
14981497α-Muurolene0.3
15181518δ-Cadinene0.80:100
15241524Dihydroactinidiolide0.4
15581557Germacrene B0.6
15601561(E)-Nerolidol0.50:100
156715661,5-Epoxysalvial-4(14)-ene0.9
15761576Spathulenol2.5
15811577Caryophyllene oxide5.9
1584---Unidentified a2.0
15911593Salvial-4(14)-en-1-one1.2
16081611Humulene epoxide II1.3
16211620epi-Cedrol1.8
16271629iso-Spathulenol1.6
16541655α-Cadinol1.6
Monoterpene hydrocarbons29.8
Oxygenated monoterpenoids7.2
Sesquiterpene hydrocarbons38.7
Oxygenated sesquiterpenoids17.3
Benzenoid aromatics0.8
Others3.7
Total identified97.4
RIcalc = retention indices calculated with respect to a homologous series of n-alkanes on a ZB-5 column. RIdb = retention indices from the databases [29,30,31,32]. ED = enantiomeric distribution (dextrorotatory enantiomer/levorotatory enantiomer). a MS(EI): 220(19%), 202(16%), 178(18%), 177(33%), 164(29%), 159(71%), 149(37%), 135(45%), 131(34%), 121(44%), 117(48%), 107(75%), 105(66%), 93(100%), 91(97%), 81(50%), 79(69%), 77(50%), 67(47%), 55(65%), 43(56%), 41(78%).
Table
Table 6. Chemical composition of Pycnanthemum incanum aerial parts essential oil.
Table 6. Chemical composition of Pycnanthemum incanum aerial parts essential oil.
RIcalcRIdbCompound%ED, (+):(−)[20]
933933α-Pinenetr 29:71
972971Sabinene0.50:100
978978β-Pinene0.10:100
9799781-Octen-3-ol3.10:1000:100
989989Myrcene0.3
10181017α-Terpinene0.1100:0
10251024p-Cymene0.8
10301030Limonene1.20:100
103210301,8-Cineole30.7
10361034(Z)-β-Ocimene0.1
10461046(E)-β-Ocimene0.2
10581058γ-Terpinene0.6
10701069cis-Sabinene hydrate5.67.2:92.8
10861086Terpinolene0.2
11001099Linalool0.3 95:5
11011099trans-Sabinene hydrate3.036.5:63.5
11251124cis-p-Menth-2-en-1-ol0.2
11421139trans-p-Menth-2-en-1-ol0.1
11561156Menthone0.2 0:100
11641165Isomenthone1.0100:0100:0
11701170δ-Terpineol2.6
11711170Borneol8.20:100
11801180Terpinen-4-ol1.833.1:66.9
11951195α-Terpineol16.929.2:70.815:85
12371237Pulegone1.8100:0100:0
12831282Bornyl acetate0.20:100
12891289Thymol0.3
13311331Bicycloelemene0.1
13351335δ-Elemene0.60:100
13751375α-Copaene0.2100:0
13831382β-Bourbonene0.2
13891390trans-β-Elemene0.347.0:53.0
14181417(E)-β-Caryophyllene11.0100:0
14291430β-Copaene0.1
14541453α-Humulene0.5
14791480Germacrene D5.090.9:9.1
14941497Bicyclogermacrene0.3
15031504(E,E)-α-Farnesene0.2
15171520δ-Cadinene0.30:100
15571557Germacrene B0.1
15591561(E)-Nerolidol0.10:100
15751576Germacrene D-4-ol0.1
15801577Caryophyllene oxide0.3
16371639cis-Guaia-3,9-dien-11-ol0.3
Monoterpene hydrocarbons4.3
Oxygenated monoterpenoids72.9
Sesquiterpene hydrocarbons18.8
Oxygenated sesquiterpenoids0.9
Others3.1
Total identified100.0
RIcalc = retention indices calculated with respect to a homologous series of n-alkanes on a ZB-5 column. RIdb = retention indices from the databases [29,30,31,32]. ED = enantiomeric distribution (dextrorotatory enantiomer/levorotatory enantiomer). tr = trace (<0.05%).
Table
Table 7. Essential oil composition of Smallanthus uvedalia from South Carolina.
Table 7. Essential oil composition of Smallanthus uvedalia from South Carolina.
RIcalcRIdbCompound%ED, (+):(−)
801801Hexanal0.1
844842Isovaleric acid1.7
849850(2E)-Hexenal0.6
851853(3Z)- Hexenol0.1
922923Tricyclenetr
925925α-Thujene0.119.1:80.9
935933α-Pinene23.96.7:93.3
948950Camphene0.4100:0
952953Thuja-2,4(10)-dienetr
960960Benzaldehyde0.1
972972Sabinene3.418.3:81.7
977978β-Pinene0.930.7:69.3
988989Myrcene1.0
10161017α-Terpinene0.1
10241025p-Cymenetr
10301030Limonene6.195.2:4.8
10311031β-Phellandrene0.2100:0
103210321,8-Cineoletr
10331033Benzyl alcoholtr
10341034(Z)-β-Ocimenetr
10421043Benzene acetaldehyde0.1
10451045(E)-β-Ocimene0.4
10571057γ-Terpinene0.2
10691069cis-Sabinene hydrate0.10:100
10841086Terpinolene0.1
10891091p-Cymenenetr
10911091Rosefuran0.1
11011098Perillene14.5
11021101trans-Sabinene hydrate0.10:100
11051104Nonanaltr
11111111Phenethyl alcohol0.1
11121113(E)-1,4-Dimethylnona-1,3,7-triene0.2
11211121trans-p-Mentha2,8-dien-1-oltr
11241124cis-p-Menth-2-en-1-oltr
11261125α-Campholenal0.1
11391140trans-Pinocarveol0.1
11411141cis-Verbenol0.1
11451145trans-Verbenol0.4
11611164Pinocarvone0.1
11701171p-Mentha-1,5-dien-8-oltr
11791180Terpinen-4-ol0.428.8:71.2
11861186p-Cymen-8-oltr
11941195α-Terpineol0.234.5:65.5
12051205Verbenone0.189.3:10.7
12171218trans-Carveol0.1
12881289Thymol0.1
13311334Bicycloelemene0.2
13351336δ-Elemene0.1
13511356Eugenol0.1
13591361Neryl acetate0.1
13751375α-Copaene0.1100:0
13781379(E)-β-Damascenone0.1
13821383cis-β-Elemene0.1
13831382β-Bourbonene0.5
13861385α-Bourbonenetr
13871387β-Cubebenetr
13891390trans-β-Elemene1.017.1:82.9
14031405(Z)-β-Caryophyllenetr
14151416cis-α-Bergamotenetr
14231424(E)-β-Caryophyllene16.9100:0
14291427γ-Elemene1.3
14331432trans-α-Bergamotene0.1
14381438Aromadendrene0.1
14411444Guaia-6,9-diene0.3
14431447iso-Germacrene D0.1
14481447Geranyl acetone0.1
14501453ε-Muurolene0.1
14551454α-Humulene1.1
146714649-epi-(E)-Caryophyllenetr
14761478γ-Muurolene0.2
14831480Germacrene D12.296.4:3.6
14891489β-Selinenetr
14901493Phenethyl isovalerate0.1
14921490γ-Amorphenetr
14951497Bicyclogermacrene1.9
14981497α-Muurolene0.1
15021504Epizonarene0.1
15041505(E,E)-α-Farnesene0.2
15071508β-Bisabolene0.1
15121512γ-Cadinene0.1
15171518δ-Cadinene0.30:100
15261528(E)-γ-Bisabolene0.2
15361538α-Cadinene0.1
15361531(Z)-Nerolidol0.1
15481549α-Elemol0.1
15581557Germacrene B2.1
15611560(E)-Nerolidol0.334.1:65.9
15761576Spathulenol0.9
15811577Caryophyllene oxide1.3
16311630Caryophylla-4(12),8(13)-dien-5α-ol0.1
16361636Caryophylla-4(12),8(13)-dien-5β-ol0.2
16411640τ-Cadinol0.1
16431644τ-Muurolol0.1
16541655α-Cadinol0.4
16571660Selin-11-en-4α-ol (=Kongol)0.1
16831683Germacra-4(15),5,10(14)-trien-1α-ol0.1
17151715Pentadecanal0.1
18411841Phytone0.2
20202022(E,E)-Geranyl linalool0.1
Monoterpene hydrocarbons36.7
Oxygenated monoterpenoids16.5
Sesquiterpene hydrocarbons39.2
Oxygenated sesquiterpenoids3.8
Diterpenoids0.1
Benzenoid aromatics0.4
Others3.2
Total identified99.9
RIcalc = retention indices calculated with respect to a homologous series of n-alkanes on a ZB-5 column. RIdb = retention indices from the databases [29,30,31,32]. ED = enantiomeric distribution (dextrorotatory enantiomer/levorotatory enantiomer). tr = trace (<0.05%).
Table
Table 8. Essential oil compositions of three samples of wild-growing Verbena hastata.
Table 8. Essential oil compositions of three samples of wild-growing Verbena hastata.
RIcalcRIdbCompoundPercent Composition
#1#2#3
801801Hexanal0.40.2---
850853(3Z)-Hexenol0.80.6---
902905Heptanal1.10.3---
960960Benzaldehyde0.30.4---
9749731-Octen-3-one0.70.3---
9779781-Octen-3-ol29.122.52.4
9839843-Octanone0.20.2---
9889892-Pentylfuran0.3------
9919956-Methyl-5-hepten-2-ol0.30.2---
9959963-Octanol0.30.2---
10021005Octanal0.30.1---
10221025p-Cymene---0.5---
10271030Limonene---0.1---
10321033Benzyl alcohol0.30.90.3
10681069cis-Linalool oxide (furanoid)---0.7---
106810761-Octanol1.0---0.6
10831082Terpinolene---0.1---
10841086trans-Linalool oxide (furanoid)---0.30.1
10981101Linalool1.51.90.7
11031104Nonanal11.11.82.0
11101111Phenyl ethyl alcohol1.72.31.2
11841186p-Cymen-8-ol---0.20.1
11891190Methyl salicylate0.41.00.4
11931195α-Terpineol---0.30.3
11961197Methyl chavicol (=Estragole)1.00.32.8
12041206Decanal---0.20.2
12141217Coumaran---0.20.5
12161219β-Cyclocitral---0.50.2
12631263(2E)-Decenal0.30.10.2
12671272Nonanoic acid0.81.02.6
12741271Decanol0.3---0.6
12901293Thymol0.30.21.1
12981300Carvacrol0.30.10.4
130913094-Vinylguaiacol---0.20.6
13511356Eugenol---0.30.3
13781380(E)-β-Damascenone0.50.80.9
14081410Italicene------0.4
14471447Geranyl acetone0.30.60.6
146114614,6,8,10-Tetramethyltridecane 0.80.30.7
14771481(E)-β-Ionone0.60.80.8
148014805,6-Epoxy-β-ionone0.30.70.4
15241524Dihydroactinidiolide0.50.91.2
15601560(E)-Nerolidol------0.2
15961596Fokienol0.31.01.1
16001600Hexadecane0.3---0.2
16281627Eremoligenol0.3---0.2
16301632γ-Eudesmol1.0---1.1
16381640Hinesol0.2------
16532656β-Eudesmol2.10.91.8
16901694Germacrone---0.4---
17141715Pentadecanal0.3---0.4
17581758Myristic acid---0.8---
18401841Phytone4.43.17.3
18661869Benzyl salicylate1.12.01.8
18891891Hexadecatrienal------0.3
19041902(E,E)-6,10,14-Trimethyl-5,9,13-pentadecatrien-2-one------0.3
19211921Methyl palmitate------0.3
19591958Palmitic acid8.521.615.3
20192018Octadecanal0.2---0.4
208220811-Octadecanol9.62.814.0
20942098Methyl linolenate------0.3
21062106Phytol5.27.112.6
21282128Linoleic acid---0.80.6
21322134α-Linolenic acid1.14.43.2
23002300Tricosane0.70.51.0
25002500Pentacosane0.40.40.6
27002700Heptacosane0.40.30.5
Monoterpenoids2.04.92.9
Sesquiterpenoids3.92.34.9
Diterpenoids5.27.112.6
Benzenoids4.97.57.9
Others75.766.358.1
Total identified91.788.286.5
Enantiomeric distribution (+):(−)
1-Octen-3-ol0:1000:1000:100
Linalool22.9:77.122.2:77.822.7:77.3
α-Terpineol49.6:50.449.8:50.249.9:50.1
(E)-β-Ionone100:0100:0100:0
(E)-Nerolidol0:1000:1000:100
RIcalc = retention indices calculated with respect to a homologous series of n-alkanes on a ZB-5 column. RIdb = retention indices from the databases [29,30,31,32].
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Lawson, S.K.; Satyal, P.; Setzer, W.N. The Volatile Phytochemistry of Seven Native American Aromatic Medicinal Plants. Plants 2021, 10, 1061. https://doi.org/10.3390/plants10061061

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Lawson SK, Satyal P, Setzer WN. The Volatile Phytochemistry of Seven Native American Aromatic Medicinal Plants. Plants. 2021; 10(6):1061. https://doi.org/10.3390/plants10061061

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Lawson, Sims K., Prabodh Satyal, and William N. Setzer. 2021. "The Volatile Phytochemistry of Seven Native American Aromatic Medicinal Plants" Plants 10, no. 6: 1061. https://doi.org/10.3390/plants10061061

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