Tansy (Tanacetum vulgare L.)—A Wild-Growing Aromatic Medicinal Plant with a Variable Essential Oil Composition

Abstract

Tansy (Tanacetum vulgare L.) is an aromatic medicinal plant whose use is limited by the presence of toxic thujone. This research aimed to evaluate the morphological and chemical properties of tansy plants growing in various natural habitats. The research determined the content and chemical composition of the essential oil, the contents of flavonoids and phenolic acids, and the antioxidant activity levels of methanol extracts from tansy inflorescences. The highest amount of essential oil (1.05 mL·kg⁻¹) was found in the raw material collected from the reclaimed area (R). Forty-seven compounds were identified in tansy oil, among which camphor (31.21–1.27%) and trans-chrysanthenyl acetate (76.09–0.09%) dominated, while the concentration of trans-thujone was low (2.67% on average). The highest amounts of flavonoids (0.52%) were found in the raw material collected from the ruderal (W) and reclaimed (R) sites, while the highest amount of phenolic acids (2.42%) was found in the raw material from the ruderal site (W). Tansy inflorescence extracts showed high antioxidant potential (88.41%). The reasons for the variability of the chemical composition of tansy were environmental and genetic variability factors.

1. Introduction

Tansy (Tanacetum vulgare L., syn. Chrysanthemum vulgare L.) is an intensely aromatic plant from the Asteraceae family, native to Europe and Asia, where it grows along roadsides, hedges, and wastelands. Medicines are made from the flower baskets of tansy (Tanaceti flos) and tansy herb (Tanaceti herba) containing 0.1–1.9% of essential oil, phenolic acids, flavonoids (derivatives of quercetin and luteolin), bitterness, and mineral compounds [1,2,3]. Tansy oil has a variable composition; its main components are beta-thujone, isomers, terpenes, camphene, beta-pinene, and others [4,5,6]. It is a yellowish-orange oily liquid with a warm, almost savory, spicy, dry, herbal odor. The oil accumulated in the flowers and leaves has a similar chemical composition. However, in some cases, the oil of the 1,8-cineole chemotype is accumulated in the leaves, and the inflorescences contain camphor oil or myrtenol oil. The content of 1,8-cineole in leaf oils is usually higher than in flower oils [1]. Stevović et al. [7] suggest that the variable composition of tansy essential oil is related to the high adaptability of this species to the environment. Coté et al. [8] report that T. vulgare essential oil has interesting biological properties, including anti-inflammatory, antioxidant, antibacterial, and cytotoxic effects.

T. vulgare is a poisonous plant, which was formerly used as a diuretic and antiparasitic drug. Due to the toxic effects of β-thujone, tansy flower extracts are mainly used externally as antiparasitic agents. In the traditional medicine of Southeast Serbia, tansy tea is used as an anthelmintic, carminative, antispasmodic, digestive-stimulant, antidiabetic, diuretic, and antihypertensive agent. Moreover, T. vulgare is conventionally used in lotions, cosmetics, dyes, insecticides, drugs, and preservatives [1]. Derda et al. [9] showed that alcoholic extracts of dried tansy herb have therapeutic properties against pathogenic and non-pathogenic strains of Acanthamoeba spp. and can be used with antibiotics to treat acanthamoeba keratitis. Devrnja et al. [10] showed that tansy extracts and low-thujone essential oil could be promising and effective alternatives in antimicrobial applications and food preservation. In subsequent studies [11], the authors suggested the potential of tansy plants to produce valuable chemicals in in vitro culture. Alizadeh et al. [12] indicated the still-existing folk and medical uses of tansy, and they even expressed concern that the intensive extraction of raw materials from natural habitats may cause the degradation of the plant’s genetic resources.

In this study, we perform a morphological and chemical assessment of wild tansy plants, considering a comparative analysis of the content and composition of the essential oil of plants growing in various habitats. We also determine the contents of flavonoids and phenolic acids and the antioxidant activity of methanol extracts from tansy flowers.

2. Materials and Methods

2.1. Plant Materials and Natural Habitats

The research object was tansy plants (Tanacetum vulgare L.) growing in natural positions in eastern Poland (Wohyń Commune, Radzyń Poviat, Lubelskie Voivodeship) (

Table 1. Description of natural tansy sites covered in the research.

Collection Site	Geographical Coordinates	Collection Site Description
R	51°45′13″ N 22°45′46″ E	Land under reclamation, adjacent to the former landfill. Sandy loam, fawn, light-colored soil with an admixture of rusty, periodically flooded with excess rainwater, classified as agricultural wasteland. Soil pH 5.5; fairly high light exposure. Tansy plants in a compact arrangement among sand reed (Calamagrostis epigejos (L.) Roth).
M	51°45′33″ N 22°46′54″ E	A meadow bordering the Bobrówka River. The stand on a small slope, located about 40 m from the river bed. Black fertile, humus soil with a pH 7.5, classified as a class IV meadow. High exposure to sunlight. The plant arrangement is moderately compact.
W	51°44′56″ N 22°47′24″ E	Ruderal position. Undeveloped area, after removing the top layer of soil, periodically dry, with high exposure to sunlight, classified as an agricultural wasteland. Light-colored sandy loam soil, pH 5. Plant arrangement free, loose, in proximity to field clover (Trifolium arvense L.)
T	51°45′28″ N 22°46′1″ E	A shallow ditch by a road with moderate traffic, adjacent to the plot classified as arable land of class V. Brown-sandy soil, not uniformly brown, pH 7. Moderate exposure to sunlight. The plant arrangement is moderately compact, with individuals of carrot (Daucus carota L.) nearby.

). The plants had been botanically identified at the Department of Botany and Plant Physiology, University of Life Sciences in Lublin. Four sites were selected for the occurrence of tansy in larger clusters, characterized by different parameters (Table 1). The choice of the habitats was made based on the possibility of obtaining a representative sample of the raw material, the different soil conditions, the distances between the sites, and the visual assessment of the condition of the plants (Figure S1).

The area covered by the research is classified as the Masovian–Podlasie climatic region, the characteristic feature of which is the influence of the continental climate. The region typically experiences varied air temperature and large diurnal amplitudes, early and relatively long summers with a predominance of eastern winds, and a long winter with a predominance of frosty winds from the eastern direction [13].

Biometric measurements were made on 1 August 2017. The area of each plant cluster was determined (R–3.4 × 4.0 m, S–2.5 × 5.5 m, H–2.6 × 3.9 m, T–1.3 × 8.8 m). Morphological characteristics of tansy plants were assessed using the frame method, by analyzing the objects and collecting plant material from an area measuring 1 m². Fifteen plants were randomly selected from each position, determining the height of the above-ground parts of the plant (from the soil surface to the top of the inflorescence), and then the inflorescences were cut manually (from the upper 4–5 cm of the shoot). Healthy, well-developed, colored, fully developed inflorescences, free from diseases and pests, were collected. After harvesting and determining the fresh weight of inflorescences, the raw material was dried in natural conditions, without access to light and with good air circulation (drying time was five days), and then weighed to assess the drying of the raw material. The drying ability of the tansy raw material was presented in the form of the dryness coefficient due to the more frequent use of this form of its presentation [14], by dividing the yield of fresh raw material by the yield of air-dried raw material.

2.2. Chemical Analyses

The air-dried tansy inflorescences (Figure S2) were subjected to chemical analyses, determining the content and composition of essential oils, flavonoids, and phenolic acids and the antioxidant activity of the extracts. All chemical analyzes were repeated in triplicate. All reagents and solvents were analytical-grade chemicals from Merck (Darmstadt, Germany), Sigma Chemical Co. (St. Louis, MO, USA), or POCH (Gliwice, Poland).

2.3. Essential Oil Extraction

Here, 20 g dried samples were subjected to water distillation for 3 h using Clevenger’s apparatus [15]. The oils were dried with anhydrous sodium sulfate, filtered, and stored in a freezer at −20 °C until the time of analysis.

2.4. Qualitative and Quantitative Analyses of an Essential Oil

For qualitative and quantitative analysis, an ITMS Varian 4000 GC-MC/MS instrument (Varian, Palo Alto, CA, USA) was used, equipped with a CP-8410 auto-injector and a 30 m × 0.25 nm i. d. VF-5ms column (Varian, Palo Alto, CA, USA), under the following conditions: film thickness = 0.25 μm; carrier gas = helium at a rate of 0.5 mL/min; injector and detector temperatures = 220 °C and 200 °C, respectively; split ratio = 1:100; injector volume = 1 μL. A temperature gradient was applied (50 °C for 1 min, then incremented by 4 °C/min to 250 °C and held at this temperature for 10 min) as follows: ionization energy = 70 eV; mass range = 40–1000 Da; scan time = 0.8 s. The linear retention indices from temperature programming, using the definition of Van den Dool and Kratz [16], were determined for a series of n-alkanes (C₆–C₄₀). The qualitative analysis was carried on the basis of MS spectra, which were compared with the spectra from the NIST library [17] and with data available in the literature [18]. The identities of the compounds were confirmed by their retention indices, as taken from the literature [18] and from our own data. The quantitative composition of the volatile oil was determined by assuming that the total of the percentages of all oil components was 100%.

2.5. Flavonoid Determination

Flavonoids were determined using the Christ-Müller method [19]. For preparation of the stock solution, we weighed 1 g of the comminuted raw material, which was placed in a round-bottom flask, then 20 mL of acetone, 2 mL of 25% hydrochloric acid (289 g/L), and 1 mL of an aqueous urotropine (methenamine) solution (5 g/L) were added and kept for 30 min in a boiling water bath under a reflux condenser. The hydrolyzate was filtered through cotton wool into a 100 mL volumetric flask. The pad with cotton wool was placed in the flask, 20 mL of acetone was added, and it was refluxed again for 10 min. The extraction was repeated, filtering the extract into the same volumetric flask and bringing the volume up to 100 mL. Then, 20 mL of the solution was introduced into a separating funnel, 40 mL of distilled water was added, and the mixture was extracted twice with ethyl acetate into 20 mL portions. The resulting organic layers were filtered through cotton wool into a 50 mL volumetric flask and supplemented with ethyl acetate. Three samples of the test solution were prepared for each analyzed raw material collected from different stands. To 10 mL of the stock solution we added 2 mL of aluminum chloride methanol solution (20 g/L), bringing the volume up to 25 mL with a mixture (1:19) of acetic acid (1.02 kg/L) and methanol. A reference solution was prepared by supplementing 10 mL of the stock solution with a mixture (1:19) of acetic acid (1.02 kg/L) and methanol. After 45 min, the absorbance of the solutions was measured in a spectrometer at a wavelength of 425 nm, zeroing the apparatus against the reference solution. The total content of flavonoids converted to quercetin was calculated according to the following formula: X = (A·0.875)/m, where A is the absorbance value of the tested solution and m is the weight of the raw material sample.

2.6. Phenolic Acids Determination

The method determined the total content of phenolic acids based on the proportional increase in color intensity of the solution relating to the content of phenolic acids in the test [20]. To prepare the sample, the crushed, sieved, and dried raw material was placed in a 250 mL round-bottom flask, then extracted three times with 50 mL of methanol in a water bath under a reflux condenser. The plant material was filtered off, methanol extracts from triplicate were mixed, and the solvent was distilled under reduced pressure. The residues were dissolved in 20 mL of hot water and left in the refrigerator for 12 h. Precipitated ballast materials were filtered on filter paper and the solutions were transferred to volumetric flasks, bringing the volume up to 100 mL with distilled water. The test solution was prepared by measuring 1 mL of the previously obtained solution, 1 mL of distilled water, 1 mL of 0.5 M hydrochloric acid, and 1 mL of Arnov’s reagent (10 g of sodium molybdate and 10 g of sodium nitrite dissolved in water and supplemented to 100 mL) into measuring tubes with a capacity of 10 mL. After 6 min, 1 mL of 0.1 M sodium hydroxide was added, supplemented with 5 mL of distilled water. The mixture was quantitatively transferred to 1 mL cuvettes and determined spectrophotometrically at 490 nm. The total contents of phenolic acids in terms of caffeic acid were calculated according to the following formula: X = (A·3.5087)/m, where A is the absorbance value of the solution and m is the raw material weight.

2.7. Antioxidant Activity

Determination of the antioxidant activity (AA) of the tansy inflorescence extract was performed using the method described by Yen and Chen [21], consisting of colorimetric measurements of the reduction degree of the DPPH radical (2,2-diphenyl-1-picrylhydrazyl). The radical solution was prepared by weighing 0.012 g of 2,2-diphenyl-1-picrylhydrazyl and quantitatively transferring this to a 100 mL volumetric flask made up of methanol (100%). The material was dissolved in an ultrasonic bath for 15 min. A blank (A_r) was performed by measuring 1 mL of distilled water (pH > 5), 3 mL of methanol (100%), and 1 mL of DPPH solution. After stirring, the spectrometer gave a reading (λ = 517 nm) after 10 min. The test sample (A_t) was prepared by measuring and combining 1 mL of sample, 3 mL of methanol (100%), and 1 mL of DPPH solution. After 10 min, the result was read at λ = 517 nm against methanol (100%). The following formula was used for the calculation: % DPPH = 100 − [A_t/A_r·100], where A_t is the absorbance of the test sample and A_r is the absorbance of the blank sample, which was 0.740.

2.8. Statistical Analysis

The results of the morphological and chemical analyses were statistically processed using the analysis of variance method. Tukey’s test was used to evaluate the differences, while the confidence intervals were calculated at the significance level of 0.01. All calculations and analyses were performed using Statistica 9.0 PL software (StatSof Inc., Tulsa, OK, USA).

3. Results

The wild-growing tansy plants were upright, leafy (large, pinnate, petiole, dark green leaves), and slightly branched at the top, ending with umbel inflorescences, with an even diameter of about 1 cm. The flowers in the inflorescences were dark yellow. Whole plants had an intense, balsamic fragrance. The tansy plants were characterized by relatively strong growth (average height of 105 cm), except for plants from the ruderal (W) site (

Table 2. Plant height and inflorescence weight values of wild-growing tansy plants.

Collection Site *	Plant Height	Range	V ** (%)	Fresh Matter	Air-dry Matter	Rd ***
	(cm)			(g·Plant−1)
R	141.0 a	129–151	4.3	685.0 a	89.0 a	7.7
M	120.8 b	109–127	3.6	588.5 a	76.5 a	7.6
W	36.9 c	19–62	36.6	562.2 a	73.0 a	7.7
T	121.4 b	117–125	1.9	590.7 a	76.8 a	7.6
Mean	105.0			595.0	77.5	7.6

* The description of the collection site is given in Table 1; ** coefficient of variation V = s/x ^. 100%, where s is the standard deviation of the sample, x is the arithmetic mean of the sample, x ≠ 0; *** R_d is the the raw material drying index calculated as the quotient of the weights of the fresh and dry raw materials; the means marked with the same letter do not differ significantly.

). By analyzing the height of tansy plants and based on the calculated coefficient of variation V, it can be concluded that three of the selected sites were characterized by little variability, while the population growing on the ruderal site (W) was heterogeneous. The fresh weight of tansy inflorescences and the weight of the dried material did not differ significantly. The dryness of the analyzed material of tansy was even and averaged 7.6.

The tested raw material of tansy varied regarding the content of polyphenols (

Table 3. Polyphenol content (%) and antioxidant activity (%) values of tansy inflorescences extracts.

Collection Site *	Total Flavonoids	Total Phenolic Acids	Antioxidant Activity **
R	0.49 ab	1.87 c	88.69 a
M	0.45 b	2.15 b	87.48 b
W	0.52 a	2.42 a	88.42 a
T	0.38 b	1.68 c	88.78 a
Mean	0.46	2.03	88.41

* The description of the collection site is given in Table 1; ** DPPH inhibition value; means marked with the same letter do not differ significantly.

). The highest amounts of flavonoids (0.52%) were found for the raw material collected from the ruderal (W) and reclaimed (R) sites, and the highest amount of phenolic acids (2.42%) was found in the raw material from the ruderal site (W). The antioxidant activity (AA) of tansy inflorescences extracts was on average 88.41%. The lowest AA (87.48%) was found in the extract from the meadow bordering the river (M).

Tansy essential oil was characterized by a light, clear, slightly aquamarine color (Figure S3) and a warm, spicy-herbal scent. The content of essential oil in the tested raw material was 0.86 mL·kg⁻¹ on average (

Table 4. Essential oil composition of wild-growing tansy plants (%).

No.	Compound	RI	Collection Site *
			R	M	W	T
1.	santolina triene	900	5.28	0.37	0.20	tr **
2.	tricyclene	919	0.42	0.14	0.12	tr
3.	α-thujene	923	0.10	0.25	0.19	tr
4.	α-pinene	930	2.09	2.08	2.29	0.78
5.	camphene	946	2.33	1.86	2.06	0.18
6.	sabinene	970	2.09	3.39	2.36	0.24
7.	β-pinene	975	0.54	0.51	0.48	tr
8.	yomogi alcohol	993	3.48	0.11	0.09	-
9.	α-terpinene	1013	0.24	0.43	0.36	0.10
10.	o-cymene	1020	0.80	0.69	1.02	0.47
11.	limonene	1024	0.85	0.53	0.64	tr
12.	1,8-cinolene	1027	7.87	5.25	6.48	2.71
13.	γ-terpinene	1050	0.61	0.79	0.71	0.20
14.	artemisia alcohol	1070	0.78	tr	-	-
15.	linalol	1089	0.33	0.33	0.28	0.17
16.	α-thujone	1095	-	tr	0.14	-
17.	trans-p-mentha-2,8-dien-1-ol	1104	-	-	-	5.39
18.	trans-thujone	1106	-	0.74	9.95	-
19.	chryasanthenone	1111	1.16	1.11	0.50	0.49
20.	cis-sabinol	1132	0.72	0.54	0.44	0.77
21.	camphor	1140	31.21	10.17	11.93	1.27
22.	pinocarvone	1157	-	1.01	-	1.12
23.	cis-chrysanthenol	1158	4.11	-	1.82	-
24.	umbellulone	1165	-	2.20	-	0.16
25.	borneol	1168	1.87	3.31	3.68	-
26.	terpinen-4-ol	1177	1.53	1.53	1.61	0.48
27.	myrtenol	1195	4.26	0.08	4.23	0.35
28.	myrtenal	1198	-	1.27	5.51	tr
29.	trans-dihydrocarvone	1204	0.23	6.61	20.62	0.10
30.	neo-iso-dihydrocarveol	1219	-	0.43	1.36	-
31.	trans-chrysanthenyl acetate	1232	0.09	37.54	0.92	76.09
32.	carvone	1245	0.65	0.51	1.44	0.06
33.	cis-chrysanthenyl acetate	1257	0.07	0.13	1.91	0.11
34.	cis-verbenyl acetate	1267	5.56	-	-	0.26
35.	bornyl acetate	1285	-	3.10	-	-
36.	neo-iso-3-thujyl acetate	1285	1.31	-	1.57	-
37.	thymol	1293	-	0.45	-	-
38.	myrtenyl acetate	1322	0.42	0.68	1.92	1.50
39.	silphiperfolg-6-ene	1366	-	-	-	0.41
40.	germacrene D	1491	0.46	0.42	0.70	0.38
41.	bicyclogermacrene	1507	0.63	tr	tr	tr
42.	E-nerolidol	1564	0.27	0.43	0.16	tr
43.	spathulenol	1579	0.78	0.90	1.07	0.56
44.	caryophyllene oxide	1584	0.85	0.50	0.97	0.45
45.	salvial-4(14)-en-1-one	1593	0.63	0.38	0.35	0.27
46.	guaiol	1611	0.56	0.51	0.83	-
47.	α-acorenol	1634	0.62	0.66	1.18	-
Essential oil efficiency (mL·kg−1)			1.05	0.8	0.9	0.7

* The description of the collection site is given in Table 1; ** <0.05.

). The richest in oil (1.05 mL·kg⁻¹) was the raw material collected from the reclaimed area (W). Forty-seven compounds were identified in the oil, among which the dominant components were camphor (31.21–1.27%) and trans-chrysanthenyl acetate (76.09–0.09%). A significant variation in the chemical composition of tansy oil was demonstrated. The share of trans-thujone in the analyzed oils was small and amounted to 2.67% on average.

The essential oil of the inflorescences obtained from the reclaimed site (R) contained the most camphor (31.21%), 1,8-cineole (7.87%), cis-verbenyl acetate (5.56%), and santolina triene (5.28%), and did not contain trans-thujone. The most abundant trans-dihydrocarvone (20.62%) and trans-thujone (9.95%) contents were found in the oil from the inflorescences of plants from the ruderal site (W). This oil also had a significant (6.48%) share of 1,8-cineole. The most common oils obtained from the inflorescences of plants growing in the meadow near the river (M) were trans-chrysanthenyl acetate (37.54%) and camphor (10.17%). These oils contained small amounts of trans-thujone (0.74%) and bornyl acetate and thymol, compounds not found in the other oils. Plants growing along the road (T) accumulated oil with the highest share of trans-chrysanthenyl acetate (76.09%), in which no trans-thujone was found. This oil contained trans-p-mentha-2,8-dien-1-ol (5.39%), which was not found in the remaining samples.

The studied tansy chemotypes were characterized by a different chemical profile for the essential oil. Two of the tested oils did not contain cis- or trans-thujone. In the remaining cases, cis-thujone constituted 0.14%, while the traces and trans-thujone constituted 0.74% and 9.95%, respectively. Plants from the reclaimed area (R) presented a camphor/1,8-cineole profile, plants growing in the meadow adjacent to the river (M) presented a trans-chrysanthenyl acetate/camphor profile, plants from the ruderal site (W) presented a trans-dihydrocarvone/camphor/trans-thujone profile, and plants growing along the road (T) presented a trans-chrysanthenyl acetate profile.

4. Discussion

The genus Tanacetum includes aromatic plant species that are highly diversified in terms of morphology and chemistry [12], as confirmed by our results. The studied natural sites of tansy (Tanacetum vulgare), with specific and different soil and climatic conditions, were characterized by a more or less heterogeneous plant population. The tallest plants came from the reclaimed site (R), where the highest essential oil yield was also found (1.05 mL·kg⁻¹). Among the studied locations, the ruderal site (W) should be noted, where the tansy plants constituted the most diverse community in terms of height, while at the same time being rich in essential oil (0.9 mL·kg⁻¹).

Tansy is an aromatic plant rich in phenolic acids, flavonoids, and their derivatives, which contribute to the plant’s pharmacological activity [1]. The herbal raw materials of tansy are the inflorescences (Tanaceti anthodium), although the literature lacks data on their chemical composition. Our research shows that wild tansy inflorescences contain essential oil (0.9%), flavonoids (0.46%), and phenolic acids (2.03%), and their concentrations depend on the type of habitat. The inflorescences collected from the most heterogeneous site regarding plant height, namely the ruderal position (W) site, turned out to be the richest in flavonoids and phenolic acids. The extracts of tansy inflorescences we obtained were distinguished by high (88.41%) antioxidant activity (AA). The AA of tansy extracts correlates well with the total polyphenol content [2,10,22]. Our results confirm that the presence of polyphenols may impact the AA of tansy inflorescence extracts.

Tansy herb (Tanaceti herba) harvested in the full flowering stage contains 0.1 to 0.5% of the essential oil [1]. In our research, the essential oil content was higher (0.7–1.05%), which could be explained by obtaining the oil from the inflorescences and not from the whole aerial parts. Tansy plants exhibit a rich chemical profile of essential oil. More than 15 different chemotypes of tansy from Scandinavia and the Baltic have been described, with most researchers identifying β-thujone, trans-thujone, camphor, and chrysanthenyl acetate as the main components of the oils of plants from various habitats around the world [1]. The tansy plants we studied did not show the thujone chemotype (67.6–71.5% α-thujone, up to 13.4% β-thujone), described by Mockute and Judzentiene [23] in the Vilnius region. Judzentiene and Mockute [24] showed that the oil obtained from inflorescences and leaves had the same dominant components of 1,8-cineole (23.6–46.3%, 11 oils), trans-thujone (35.7–78, 4%, six samples), camphor (19.8–61.8%, 17 oils), and myrtenol (13.1–24.9%, six samples). The amounts of 1,8-cineole in all leaf oils were greater than in the inflorescence oils; an inverse correlation was found for camphor, myrtenol, and cis- and trans-thujone. The inflorescence oil samples we analyzed generally contained high amounts of camphor and 1,8-cineole and low amounts of cis- and trans-thujone, myrtenol, and myrtenal. It is worth paying attention to trans-chrysnathenyl acetate, a significant share of which (37.54 and 76.09%) was determined for two tansy chemotypes. This compound is present in tansy oil within wide limits (0–41.62%) and is not often described as the dominant component [1]. Di Napoli et al. [25] showed that the oil extracted from Anthemis secundiramea flowers containing (+)-(E)-chrysanthenyl acetate has antimicrobial properties against Gram-positive and Gram-negative bacteria, inhibits biofilm formation, has antioxidant activity, and may have antimicrobial properties, which are potentially relevant for topical, cosmetic, and nutraceutical applications.

Chemical polymorphism, which modifies the production of secondary metabolites among aromatic plants, is a widely described phenomenon [4,26]. Several aromatic plant chemotypes have been identified, but they have not yet been unequivocally linked to possible causes [26]. The tansy habitats we examined differed in terms of soil type, fertility and reaction, light conditions, and humidity conditions. M and W were found to be the best in terms of light conditions, and in terms of humidity R and M were best. Light is responsible for increasing the concentrations of monoterpenes and phenylpropanes [27,28]. The opposite is sometimes reported, whereby the concentrations of camphene, sabinene, β-pinene, borneol, bornyl acetate, and Z-jasmone may be higher in plants grown in partial shade than in full light [29]. Increased water availability stimulates the production of monoterpenes [30,31], although some data indicate a possible increase in monoterpenes with low water availability [32]. In our research, trans-chrysanthenyl acetate, a representative of monoterpenes, dominated (37.54 and 76.09%) in the oil of two tansy chemotypes from M and T, with different light and humidity conditions. Plants presenting a mixed trans-chrysanthenyl acetate/camphor profile, on the other hand, came from the places with the best light and humidity conditions. Palà-Paùl et al. [33] found that the distribution of terpenes was influenced by soil pH; the population of Erygium campestre (Apiaceae) growing in acidic soil contained more myrcene and significantly less β-curcumene than the population growing in alkaline soil. Our research shows that more trans-chrysanthenyl acetate was accumulated by plants growing in alkaline and neutral soils rather than acidic soil. The share of camphor in tansy oil was higher in plants inhabiting acidic sites than in other plants. The concentration of 1,8-cineole, known for its antimicrobial activities [34], was higher (7.87% and 6.48%) in the plant oil in the acidic position than in the alkaline (5.25%) and neutral (2.71%) positions. Likewise, another representative of the trans-dihydrocarvone monoterpenoids dominated (20.62%) in the plant oil of the acid territory. The main limitation in using tansy oil and the raw material is the presence of thujone. Formisano et al. [35] described T. vulgare subsp. siculum as a thujone chemotype, suggesting that the high thujone content could explain the high sun exposure of plants. Our results confirmed that the chemotype containing the highest amount of thujone in the oil (9.95%) came from a habitat with high light exposure.

On the other hand, plants found in environmentally different places were characterized by similar amounts of camphor, which may suggest genetic reasons. Oils containing similar amounts of camphor (10.17 and 11.93%) were obtained from plants t M and W sites with different environmental conditions, being alkaline and acidic soils, respectively, with high and moderate light exposure. At the same time, different levels of camphor (31.21 and 11.93%) were characteristic for plants of similar areas in terms of environmental conditions (R and W). Another example is trans-dihydrocarvone, occurring in higher amounts (6.61 and 20.62%) in plant oils from different environmental areas (M and W). Therefore, it can be assumed that the concentration of camphor or trans-dihydrocarvone in tansy oil is modified to a lesser extent by environmental factors, such as genetic factors. Hyeon et al. [36] showed that the differences and correlations of essential oil components, phenolic acids, and primary metabolites depended on common or closely related metabolic pathways, which supports the above supposition.

An essential aspect of this problem is the adaptability of tansy, which is most likely related to the presence of certain compounds in the oil [7]. According to these authors, the amount and composition of the essential oils of plants growing in industrial areas and in green areas can serve as indicators of the adaptability of this species to anthropocentric and anthropogenic environmental conditions and its usefulness. Our results for the varied tansy chemotypes from a reclaimed meadow, ruderal, and roadside sites strongly support this hypothesis. The protective role of volatile substances should also be considered here, an example of which is the increased levels of terpenoids (in particular L-camphor) in response to the presence of pests [37].

5. Conclusions

The wild-growing tansy plants turned out to be a valuable and varied source of bioactive substances. Tansy inflorescence extracts showed high antioxidant potential. The reasons for the variability of the chemical composition of tansy can be found in the environmental and genetic variability; therefore, further research should include molecular analyses.

Inflorescences collected from the most heterogeneous sites regarding plant height (ruderal area (W)) were the richest in flavonoids and phenolic acids. The essential oil of these inflorescences contained the most toxic trans-thujone, although this value did not exceed 10%. The highest plant inflorescences from the reclaimed area (R) showed the highest essential oil yield.

The tansy plants examined here presented 4 chemotypes: camphor/1,8-cineole, trans-chrysanthenyl acetate/camphor, trans-dihydrocarvone/camphor/trans-thujone, and trans-chrysanthenyl acetate. Particularly interesting was the thujone-free chemotype, rich in 1,8-cineol and camphor, and the equally interesting chemotype of trans-chrysanthenyl acetate, also without thujone.