Acessibilidade / Reportar erro

Growth and production of volatile compounds of yarrow (Achillea millefolium L.) under different irrigation depths

Abstract

Yarrow (Achillea millefolium L., Asteraceae) is an important medicinal plant used worldwide for its medicinal properties such as the analgesic, antioxidant and anti-inflammatory ones. The aim of this study was to evaluate the growth and production of photosynthetic pigments and of volatile constituents of Achillea millefolium L. under different irrigation depths. The treatments were the application of 55, 110, 220, 440 and 880 mm of water for a period of 110 days. Data were submitted to polynomial regression analysis at 5% probability, while the volatile constituents were analyzed by standard deviation. Different irrigation depths provided quadratic growth responses being the highest dry matter production at the depth of 440 mm. The contents of chlorophyll a, b, total and carotenoids were higher at the lower depth tested (55 mm). The major volatile compounds identified were sabinene, 1,8-cineol, borneol and β-caryophyllene. Increased water availability reduced the complexity of the volatile fraction of essential oil. Thus, it is recommended that the species be cultivated at 440 mm irrigation depth to have a higher production of dry matter and lower variation in the volatile profile of the essential oil.

Key words
water stress; 1; 8 cineol; chlorophyll; terpenes

INTRODUCTION

Yarrow (Achillea millefolium L., Asteraceae) is a perennial herb, native to Europe and growing in different countries. The species produces essential oil in its leaves and inflorescences, and is used as an analgesic, antioxidant, anti-inflammatory and is gastroprotective (Judzentiene and Mokute 2010JUDZENTIENE A and MOCKUTE D. 2010. Essential oil composition of two yarrow taxonomic forms. Cent Europ J Biol 5: 346-352.). In addition, its essential oil is used commercially in the cosmetics industry, skin care products and aromatherapy (Mohammadhosseini et al. 2017MOHAMMADHOSSEINI M, SARKER SD and AKBARZADEH A. 2017. Chemical composition of the essential oils and extracts of Achillea species and their biological activities: A review. J Ethnopharmacol 199: 257-315). This essential oil presents great diversity of chemical compounds, and caryophyllene, sabinene, γ-terpinene, borneol and chamazulene are mentioned as majoritarian (Kindlovits and Németh 2012KINDLOVITS S and NÉMETH É. 2012. Sources of variability of yarrow (Achillea spp.) essential oil. Acta Alimentaria 41(Suppl. 1) 92-103.). However, the chemical composition of its essential oil varies due to different factors. For example, Pinto et al. (2014a)PINTO JEBP, FERRAZ EO, BERTOLUCCI SKV, SILVEIRA HR, SANTOS AR and SILVA GM. 2014a. Biomass production and essential oil in yarrow cultivated under colored screen types. Hort Bras 32: 321-326. observed significant changes in the essential oil compounds of yarrow when cultivated under different light conditions; the same response was observed when there was lack of macro and microelements in a hydroponic system (Alvarenga et al. 2015ALVARENGA ICA, BOLDRIN PF, PACHECO FV, SILVA ST, BERTOLUCCI SKV and PINTO JEBP. 2015. Effects on growth, essential oil content and composition of the volatile fraction of Achillea millefolium L. cultivated in hydroponic systems deficient in macro-and microelements. Sci Horticult 197: 329-338.).

Irrigated cultivation allows medicinal plants to be grown year-round, thus providing the continuous supply of raw material. However, the plant productivity response as a function of water availability is specific, since it is related to the genetic characteristics of the plant, nutrient availability, and the ability of the plant to allocate photoassimilates (Marschner et al. 1996MARSCHNER H, KIRKBY EA and CAKMAK I. 1996. Effect of mineral nutritional status on shoot-root partitioning of photoassimilates and cycling of mineral nutrients. J Exp Bot 47: 1255-1263.). In most cases, pigments such as chlorophylls and carotenoids are rapidly degraded under water limiting conditions; however, they can also be accumulated depending on the species (Anjum et al. 2011ANJUM SA, XIE XY, WANG LC, SALEEM MF, MAN C and LEI W. 2011. Morphological, physiological and biochemical responses of plants to drought stress. African J Agricultural Res 6: 2026-2032., Manivannan et al. 2007MANIVANNAN P, JALEEL CA, SANKAR B, KISHOREKUMAR A, SOMASUNDARAM R, LAKSHMANAN GA and PANNEERSELVAM R. 2007. Growth, biochemical modifications and proline metabolism in Helianthus annuus L. as induced by drought stress. Colloids Surf B Biointerfaces 59: 141-149.).

The species Lippia sidoides Cham., cultivated under water limitation, for example, showed a reduction in the production of dry matter and essential oil (Alvarenga et al. 2012ALVARENGA ICA, LOPES OD, PACHECO FV, OLIVEIRA FG and MARTINS ER. 2012. Fator de resposta do alecrim-pimenta a diferentes lâminas de irrigação. Pesq Agropec Trop 42: 462-468.). However, the moderate water limitation in a cultivation of lemongrass (Cymbopogon citratus (DC.) Stapf) increased the production of essential oil (Pinto et al. 2014bPINTO DA, MANTOVANI EC, MELO EDC, SEDIYAMA GC and VIEIRA GHS 2014b. Produtividade e qualidade do óleo essencial de capim-limão (Cymbopogon citratus, DC.) submetido a diferentes lâminas de irrigação. Rev Bras Plant Med 16: 54-61.). For basil (Ocimum basilicum L.) and tea tree (Melaleuca alternifolia Chen.), intermediate water depths have proved ideal for the production of dry matter (Silva et al. 2012SILVA SR, DEMUNER AJ, ALMEIDA BARBOSA LC, CASALI VWD, NASCIMENTO EA and PINHEIRO AL. 2012. Efeito do estresse hídrico sobre características de crescimento e a produção de óleo essencial de Melaleuca alternifolia Cheel. Acta Sci 24: 1363-1368., Pravuschi et al. 2010PRAVUSCHI PR, MARQUES PAA, RIGOLIN BHM and SANTOS ACP. 2010. Efeito de diferentes lâminas de irrigação na produção de óleo essencial do manjericão (Ocimum basilicum L.) Acta Sci, Agron 32: 687-693.).

Therefore, water availability for the production of medicinal plants alters their growth and the synthesis of secondary compounds. However, it is necessary to understand how the availability of water changes the plant metabolism, because alterations in the levels of active constituents can compromise the parameters of quality, efficacy and safety of the plant material (Baghalian et al. 2008BAGHALIAN K, HAGHIRY A, NAGHAVI MR and MOHAMMADI A. 2008. Effect of saline irrigation water on agronomical and phytochemical characters of chamomile (Matricaria recutita L.). Scientia Horticult 116: 437-441.). Misra and Srivastava (2000)MISRA A and SRIVASTAVA NK. 2000. Influence of water stress on Japanese mint. J Herbs Spices Med Plants 7: 51-58. observed significant increases in menthol and menthone levels for Mentha arvensis L. under water limitation (field moisture capacity of 10%). On the other hand, for Mentha piperita L., menthol content decreased by 36% and menthone content by 50%, under the condition of less water availability (Khorasaninejad et al. 2011KHORASANINEJAD S, MOUSAVI A, SOLTANLOO H, HEMMATI K and KHALIGHI A. 2011. The effect of drought stress on growth parameters, essential oil yield and constituent of Peppermint (Mentha piperita L.). J Med Plant Res 5: 5360-5365.). Thus, it can be observed that water availability influences both the essential oil content and its quality, yielding significant changes in the terpenic compounds. In addition, the proper irrigation management combines the production of vegetable matter with the contents of secondary metabolites (Alvarenga et al. 2012).

Due to the influence of water availability on plant production, and lack of knowledge of the response of yarrow to irrigation, the objective of this study was to evaluate the growth, production of photosynthetic pigments and of volatile constituents of Achillea millefolium L. under different irrigation depths.

MATERIALS AND METHODS

The experiment was conducted in a greenhouse, in the sector of Plant Physiology at the Department of Biology of the Universidade Federal de Lavras (UFLA). A species specialist identified the plants and deposited the exsiccatae in the Bioscience Institute of the Universidade Federal do Rio Grande do Sul, Brazil, with register number ICN 187014.

Drainage microlysimeters with capacity of 15L and mean diameter of 25 cm were used. They were filled with substrate composed of soil and sand in the ratio of 2:1, and fertilized with NPK 4-14-8 in the ratio of 2 kg per m3 of substrate. The physicochemical characteristics of the soil were analyzed at the Laboratory of Analysis of Soil of UFLA, and were: pH: 5.4; P: 4.13 mg dm-3; K: 73.32 mg dm-3, Ca: 2.30 cmolc dm-3, Mg: 0.30 cmolc dm-3, Al: 0.10 cmolc dm-3, H + Al: 2.90 cmolc dm-3; V: 49.00%; organic matter: 2.10 dag kg-1, Clay: 70.00 dag kg-1; Silt: 16.00 dag kg-1 and Sand: 14.00 dag kg-1.

To start the experiment, the microlysimeters were saturated with water, and then covered with plastic to prevent evaporation to allow the substrate to have 100% of field capacity. By the time water percolation ceased, the planting of seedlings was carried out.

The seedlings (derived from cuttings) were produced in expanded polypropylene trays filled with commercial substrate, and kept in intermittent mist chamber. After sixty days, with 10 cm of height and four expanded leaves, the seedlings were transplanted to the microlysimeters.

The treatments consisted of application of five irrigation depths: 55, 110, 220, 440 and 880 mm, distributed in daily applications during the growing period. For each treatment, five replicates were used with a plant per repetition, in a total of 25 plants, distributed in a completely randomized design. Plants from which samples were taken for chlorophyll analysis were not accounted for assessment of the production of dry matter of the aerial part and total dry matter, being used for analysis of the other variables.

The average temperature during the experiment was of 22.08 °C, with average maximum temperature of 30.91 ºC, and average minimum temperature of 13.26 °C and average relative humidity of 78.50%. The temperature and relative humidity in the greenhouse were recorded with the aid of a portable thermo-hygrometer.

After 110 days of cultivation (Netto and Raffaelli 2004NETTO SP and RAFFAELLI G. 2004. Produção experimental de mil-folhas (Achillea millefolium L.), visando à extração de óleo essencial. Rev Acad: Cien Agrarias Amb 2: 27-31.), plants were collected for evaluation of growth. The growth was evaluated through measurement of root length, stem diameter, and by counting the number of leaves and shoots. The dry matter production of the aerial part, stem and roots as well as total dry matter production were evaluated. In order to obtain the dry materials, plants were dried in a forced-air oven at 40 °C until the weight stabilized.

The photosynthetic pigments analyzed were chlorophyll a, chlorophyll b, total chlorophyll, and carotenoids. The extraction was performed from fully expanded leaf collected from five plants per treatment on the 110th day of cultivation. For the extraction, 0.2 g of fresh leaves were weighed, and homogenized with 30 mL of 80% acetone (v/v). The contents of chlorophyll a, chlorophyll b and carotenoids were calculated with the equations proposed by Lichtenthaler and Buschmann (2001)LICHTENTHALER HK and BUSCHMANN C. 2001. Chlorophylls and Carotenoids: Measurement and Characterization by UV‐VIS Spectroscopy. Cur Prot Food Analy Chem 1: F4.3.1-F4.3.8. from the absorbance readings at 663.2 nm, 646.8 nm and 470 nm, respectively. All procedures were performed in the dark and the readings were performed in triplicates.

The constituents of the volatiles were analyzed from 40 mg of dry matter of leaves, and four composite samples per treatment were utilized. Dried leaves were placed in a 20 mL headspace vial, sealed with septum silicone / PTFE. The analyses were performed with the “headspace” technique in a Gas Chromatograph coupled to a Mass Spectrophotometer (GC/MS: Agilent® 7890 A / Agilent® MSD 5975C, HP-5MS column). After optimization, the following operating conditions were established: Sample incubation temperature of 100 °C for 30 min, syringe temperature of 110 °C. The volume of 500 µL of the vapor phase was injected into the chromatographic column, in split mode at a ratio of 1:50. The volatile fraction was analyzed in an Agilent® 7890A Gas Chromatograph coupled to an Agilent® 5975C Mass Selective Detector (MSD) (Agilent Technologies, CA), operated by electron impact ionization using 70 eV, scanning mode at a scan rate of 1.0 / s, acquisition mass range of 40-400 m / z. We used an HP-5MS fused-silica capillary column (30 m length x 0.25 mm internal diameter x 0.25 mm film thickness) (California, USA). Helium was used as carrier gas with a flow rate of 1.0 ml / min; the injector temperature and the transfer line to the MS were maintained at 220 °C and 240 °C, respectively. The initial oven temperature was of 60 °C held isothermally for 1.5 min, followed by a temperature ramp of 3 °C / min until the temperature of 240 °C was reached, followed by a ramp of 10 °C / min until the temperature of 270 °C was reached.

The identification of the volatile constituents was performed by comparing retention indices relative to a standard solution of n alkanes (C8-C18) and with the mass spectra found in specialized literature (Adams 2007ADAMS RP. 2007. Identification of essential oil components by gas chromatography/mass spectrometry, 4th ed., Illinois: Allured Publish Corporation, 804 p., NIST 2008NIST - NATIONAL INSTITUTE OF STANDARDS and TECHNOLOGY. 2008. Topic detection and tracking evaluation. Online. Avaiable at: < http://webbook.nist.gov/chemistry>. (Access in Feb 15, 2015).
http://webbook.nist.gov/chemistry>....
). The retention indices were calculated using the equation proposed by Van den Dool and Kratz (1963)VAN DEN DOOL H and KRATZ PDJA. 1963. Generalization of the retention index system including linear temperature programmed gas-liquid partition chromatography. J Chromat 11: 463-471..

For the growth and production of photosynthetic pigments, the data were analyzed through the F test (p<0.05) and, when significant, polynomial regression was performed. The volatile constituents were analyzed by standard deviation (n=4) and represented in a table showing the identified compounds with their respective retention indices and relative areas (%).

RESULTS AND DISCUSSION

The plants presented significant (p<0.05) responses to the different irrigation depths, showing mostly quadratic curves. The increase in stem diameter and the number of leaves were favored with increasing water supply, and the highest values of these variables were observed for the greatest depth applied (880 mm). Meanwhile, root length was greater for the depth of 440 mm and the number of shoots was larger for the depth of 55 mm (Figure 1).

Figure 1
Stem diameter (a), number of leaves (b), root length (c) and number of shoots (d) of Achillea millefolium L. grown with application of 55, 110, 220, 440 and 880 mm irrigation depths.

The increase in stem diameter is related to the increase in the number of leaves, since the plant grows in a rosette form. The larger number of leaves, observed for the greatest depth, is a way the plant has to increase evaporation surface and improve the flow of nutrients and water (Peuke 2010PEUKE AD. 2010. Correlations in concentrations, xylem and phloem flows, and partitioning of elements and ions in intact plants. J Exp Bot 61: 635-655.). The results corroborate those observed by Meira et al. (2013)MEIRA MR, MELO MTP, MARTINS ER, PINTO MJS and SANTANA CS. 2013. Crescimento vegetativo, produção de fitomassa e de óleo essencial de Melissa officinalis L. sob diferentes lâminas de irrigação. Cienc Rural 43: 779-785., where there was an increase in these variables for the treatment with the greatest depth applied to Melissa officinalis L.

The yarrow plant ceased its root growth at the lowest water availability (55mm), unlike many species under water limiting conditions, which expend their energy on root growth and, consequently, reach deeper and wet layers of soil (Das and Kar 2018DAS S and KAR RK. 2018. Abscisic acid mediated differential growth responses of root and shoot of Vigna radiata (L.) Wilczek seedlings under water stress. Plant Physiol Biochem 123: 213-221.).

The increase in the number of shoots with the lowest water availability may be associated with hormonal imbalance between auxins and cytokinins and with a stimulating effect on shoot initiation (Fu and Harberd 2003FU X and HARBERD NP. 2003. Auxin promotes Arabidopsis root growth by modulating gibberellin response. Nature 421(6924): 740-743.).

For leaves, roots, stem and total dry matter production, a quadratic behavior of the curve was observed with increasing responses up to the depth of 440 mm (Figure 2). The reduction of dry matter production in all parts of the plant at 880 mm may be attributed to a possible excess of water in the root zone. This excess water might have led to a condition of hypoxia, which compromises the production of dry matter. Under hypoxia, the roots favor anaerobic respiration due to reduced oxygen levels and ATP generation decreases. This promotes a reduction in energy production and, consequently, in reduced overall plant growth (Hasibeder et al. 2014HASIBEDER R, FUCHSLUEGER L, FRITZ K, RICHTE A and BAHN M. 2014. Summer drought alters dynamics of carbon allocation to roots and root respiration in mountain grassland. New Phytol 205(3): 1117-1127.). The higher soil water availability also promoted reductions in dry matter production of Ocimum basilicum L. (Khalid 2006KHALID KA. 2006. Influence of water stress on growth, essential oil, and chemical composition of herbs (Ocimum sp.). Int Agrophysics 20: 289-296.).

Figure 2
Production of Achillea millefolium L. grown with application of 55, 110, 220, 440 and 880 mm irrigation depths. (a) Dry matter of aerial part (DMAP); (b) Dry matter of roots (DMR); (c) Dry matter of stem (DMS); (d) Total dry matter (TDM).

The results for dry matter production indicate that the species grows better under intermediate water conditions, with higher growth under a depth of 440 mm. Similar results, where intermediate depths were also ideal for the production of dry matter, were observed for Ocimum basilicum L. and Melaleuca alternifolia Cheel. (Silva et al. 2012SILVA SR, DEMUNER AJ, ALMEIDA BARBOSA LC, CASALI VWD, NASCIMENTO EA and PINHEIRO AL. 2012. Efeito do estresse hídrico sobre características de crescimento e a produção de óleo essencial de Melaleuca alternifolia Cheel. Acta Sci 24: 1363-1368., Pravuschi et al. 2010PRAVUSCHI PR, MARQUES PAA, RIGOLIN BHM and SANTOS ACP. 2010. Efeito de diferentes lâminas de irrigação na produção de óleo essencial do manjericão (Ocimum basilicum L.) Acta Sci, Agron 32: 687-693.). Nonetheless, it is important to notice that the species is able to survive under low water availability.

The contents of chlorophyll a, b, total chlorophyll and carotenoids were higher at the smallest depth tested (55 mm), which provided an accumulation of almost double the contents of the treatment of 440 mm (Figure 3). Pigments such as chlorophylls and carotenoids may be used as indicators of both nutritional and water stress (Reddy et al. 2004REDDY AR, CHAITANYA KV and VIVEKANANDAN M. 2004. Drought-induced responses of photosynthesis and antioxidant metabolism in higher plants. J Plant Physiol 161: 1189-1202.). Usually, under water limitation conditions, chlorophyll is rapidly degraded, which affects photosynthesis and results in production losses (Havaux and Tardy 1999HAVAUX M and TARDY F. 1999. Loss of chlorophyll with limited reduction of photosynthesis as an adaptive response of Syrian barley landraces to high-light and heat stress. Funct Plant Biol 26: 569-578.). However, in some cases, there may be an accumulation of pigments as a way to mitigate stress, which reduces the action of reactive species of oxygen and, at the same time, maintains a photosynthetic rate (Dinakar et al. 2012DINAKAR C, DJILIANOV D and BARTELS D. 2012. Photosynthesis in desiccation tolerant plants: Energy metabolism and antioxidative stress defense. Plant Sci 182: 29-41.).

Figure 3
Photosynthetic pigments of Achillea millefolium L. grown with application of 55, 110, 220, 440 and 880 mm irrigation depths. (a) Chlorophyll a; (b) chlorophyll b; (c) total chlorophyll; (d) carotenoids.

Therefore, photosynthetic pigments may work as protection against oxidative damage in yarrow. Another point to be noticed was the lowest pigment contents observed for the depth of 440 mm, which corresponded to the highest dry matter production, which may indicate an adequate adjustment of the photosynthetic apparatus. This response is corroborated by the work of Khalil et al. (2011)KHALIL SK, ST HILAIRE R, KHAN A, REHMAN A and MEXAL JG. 2011. Growth and physiology of yarrow species Achillea millefolium cv. Cerise queen and Achillea filipendulina cv. Parker gold at optimum and limited moisture. Aust J Crop Sci 5: 1698-1706. who observed that yarrow did not significantly alter its stomatal conductance under conditions of water limitation.

Table I shows the presence of 27 constituents in the composition of the volatile fraction of the essential oil of yarrow. The largest number of constituents (27) was observed for the treatment with the smallest depth (55 mm), and the smallest number of constituents (17) for the treatment with the greatest depth (880 mm). The identified volatile constituents belong to the classes of monoterpenes (contents between 47.85 and 63.64%), oxygenated monoterpenes (18.31-30.49%), sesquiterpenes (12.03-22.98%) and oxygenated sesquiterpenes (0.29-0.63%), among others (0.98-3.4%). The major constituents (Figure 4) were sabinene (32.21-50.97%), 1,8-cineol (6.05-12.85%), borneol (6.69%-13.00%) and β-caryophyllene (10.30-20.07%), as observed in studies on chemical characterization of the species (Kindlovits and Németh 2012KINDLOVITS S and NÉMETH É. 2012. Sources of variability of yarrow (Achillea spp.) essential oil. Acta Alimentaria 41(Suppl. 1) 92-103., Mohammadhosseini et al. 2017MOHAMMADHOSSEINI M, SARKER SD and AKBARZADEH A. 2017. Chemical composition of the essential oils and extracts of Achillea species and their biological activities: A review. J Ethnopharmacol 199: 257-315).

Figure 4
- Major volatile compounds of Achillea millefollium L. cutivated with application of 55, 110, 220, 440 and 880 mm irrigation depths; bars show standard deviations (n = 4).
TABLE I
Volatile compounds of Achillea millefolium L. cultivated with different irrigations depths (Relative area ±SD).

Increased water availability reduces the complexity of essential oil by reducing the number of constituents. Moreover, the conditions of lower water availability promoted an increase in the content of oxygenated monoterpenes and a decrease in the contents of sesquiterpenes. The increase in the contents of monoterpenes may be associated with a way the plant has to neutralize reactive species of oxygen. The accumulation of monoterpenes may mitigate the oxidative damage to chloroplast caused by free radicals, besides replacing photorespiration in order to protect against photooxidation under stress conditions (Peñuelas and Llusià 2002PEÑUELAS J and LLUSIÀ J. 2002. Linking photorespiration, monoterpenes and thermotolerance in Quercus. New Phytologist 155: 227-237.). The results demonstrated that the species has adaptability to conditions of low water availability. Contrary results were observed for Rosmarinus officinalis L. and Mentha spicata L., where the contents of monoterpene constituents increased with increased water availability (Delfine et al. 2005DELFINE S, LORETO F, PINELLI P, TOGNETTI R and ALVINO A. 2005. Isoprenoids content and photosynthetic limitations in rosemary and spearmint plants under water stress. Agric Ecosys Environ 106: 243-252.).

The highest sabinene content was observed for the greatest depth applied (880 mm), with an increase of approximately 70% when compared to the smallest depth, while the contents of 1,8 cineol and borneol decreased with higher water availability (880 mm). Decrease in the contents of these compounds (1,8 cineol and borneol) with higher water availability was also observed for Salvia officinalis L. and Alpinia zerumbet (Pers.) B. L. Burtt & R. M. Sm (Bettaieb et al. 2009BETTAIEB I, ZAKHAMA N, WANNES WA, KCHOUK ME and MARZOUK B. 2009. Water deficit effects on Salvia officinalis fatty acids and essential oils composition. Sci Hortic 120: 271-275., Rezende et al. 2011REZENDE ME, JASMIM JM, CAPRINI GP, SOUSA EF, SCHRIPSEMA J and THIÉBAUT JTL. 2011. Teor e composição química do óleo essencial de alpínia em razão da adubação e da disponibilidade de água no solo. Rev Ceres 58: 208-215.).

The β-caryophyllene content presented a varying response in relation to the different depths tested, being higher for the treatment with 440 mm (Figure 4). The variation in contents and the increased number of constituents under low water availability may be attributed to the activity of enzymes, from the terpene synthases family, which have the ability to transform a substrate in different products, and many of which are more active under stress conditions (Degenhardt et al. 2009DEGENHARDT J, KÖLLNER TG and GERSHENZON J. 2009. Monoterpene and sesquiterpene synthases and the origin of terpene skeletal diversity in plants. Phytochem 70: 1621-1637.).

CONCLUSIONS

The data observed in this study can make it possible to infer that yarrow presents some adaptation to low water availability conditions, such as growth stabilization and increased number of shoots, the accumulation of pigments and increased number of volatile components of the leaves, which on further studies can be used as an indicator of stress. In addition, the depth of 440 mm of water was the one that provided the greatest growth with higher aerial, root and total dry matter production of yarrow. Regarding the volatile components, it was observed that water availability affects the metabolism of terpenes; however, the major components: sabinene, borneol, 1,8 cineol and β-caryophyllene, were identified in all-treatments.

ACKNOWLEGMENTS

The authors wish to thank Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq), Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES), and Fundação de Amparo à Pesquisa do Estado de Minas Gerais (FAPEMIG) for granting scholarships and for their financial support.

REFERENCES

  • ADAMS RP. 2007. Identification of essential oil components by gas chromatography/mass spectrometry, 4th ed., Illinois: Allured Publish Corporation, 804 p.
  • ALVARENGA ICA, BOLDRIN PF, PACHECO FV, SILVA ST, BERTOLUCCI SKV and PINTO JEBP. 2015. Effects on growth, essential oil content and composition of the volatile fraction of Achillea millefolium L. cultivated in hydroponic systems deficient in macro-and microelements. Sci Horticult 197: 329-338.
  • ALVARENGA ICA, LOPES OD, PACHECO FV, OLIVEIRA FG and MARTINS ER. 2012. Fator de resposta do alecrim-pimenta a diferentes lâminas de irrigação. Pesq Agropec Trop 42: 462-468.
  • ANJUM SA, XIE XY, WANG LC, SALEEM MF, MAN C and LEI W. 2011. Morphological, physiological and biochemical responses of plants to drought stress. African J Agricultural Res 6: 2026-2032.
  • BAGHALIAN K, HAGHIRY A, NAGHAVI MR and MOHAMMADI A. 2008. Effect of saline irrigation water on agronomical and phytochemical characters of chamomile (Matricaria recutita L.). Scientia Horticult 116: 437-441.
  • BETTAIEB I, ZAKHAMA N, WANNES WA, KCHOUK ME and MARZOUK B. 2009. Water deficit effects on Salvia officinalis fatty acids and essential oils composition. Sci Hortic 120: 271-275.
  • DAS S and KAR RK. 2018. Abscisic acid mediated differential growth responses of root and shoot of Vigna radiata (L.) Wilczek seedlings under water stress. Plant Physiol Biochem 123: 213-221.
  • DEGENHARDT J, KÖLLNER TG and GERSHENZON J. 2009. Monoterpene and sesquiterpene synthases and the origin of terpene skeletal diversity in plants. Phytochem 70: 1621-1637.
  • DELFINE S, LORETO F, PINELLI P, TOGNETTI R and ALVINO A. 2005. Isoprenoids content and photosynthetic limitations in rosemary and spearmint plants under water stress. Agric Ecosys Environ 106: 243-252.
  • DINAKAR C, DJILIANOV D and BARTELS D. 2012. Photosynthesis in desiccation tolerant plants: Energy metabolism and antioxidative stress defense. Plant Sci 182: 29-41.
  • FU X and HARBERD NP. 2003. Auxin promotes Arabidopsis root growth by modulating gibberellin response. Nature 421(6924): 740-743.
  • HASIBEDER R, FUCHSLUEGER L, FRITZ K, RICHTE A and BAHN M. 2014. Summer drought alters dynamics of carbon allocation to roots and root respiration in mountain grassland. New Phytol 205(3): 1117-1127.
  • HAVAUX M and TARDY F. 1999. Loss of chlorophyll with limited reduction of photosynthesis as an adaptive response of Syrian barley landraces to high-light and heat stress. Funct Plant Biol 26: 569-578.
  • JUDZENTIENE A and MOCKUTE D. 2010. Essential oil composition of two yarrow taxonomic forms. Cent Europ J Biol 5: 346-352.
  • KHALID KA. 2006. Influence of water stress on growth, essential oil, and chemical composition of herbs (Ocimum sp.). Int Agrophysics 20: 289-296.
  • KHALIL SK, ST HILAIRE R, KHAN A, REHMAN A and MEXAL JG. 2011. Growth and physiology of yarrow species Achillea millefolium cv. Cerise queen and Achillea filipendulina cv. Parker gold at optimum and limited moisture. Aust J Crop Sci 5: 1698-1706.
  • KHORASANINEJAD S, MOUSAVI A, SOLTANLOO H, HEMMATI K and KHALIGHI A. 2011. The effect of drought stress on growth parameters, essential oil yield and constituent of Peppermint (Mentha piperita L.). J Med Plant Res 5: 5360-5365.
  • KINDLOVITS S and NÉMETH É. 2012. Sources of variability of yarrow (Achillea spp.) essential oil. Acta Alimentaria 41(Suppl. 1) 92-103.
  • LICHTENTHALER HK and BUSCHMANN C. 2001. Chlorophylls and Carotenoids: Measurement and Characterization by UV‐VIS Spectroscopy. Cur Prot Food Analy Chem 1: F4.3.1-F4.3.8.
  • MANIVANNAN P, JALEEL CA, SANKAR B, KISHOREKUMAR A, SOMASUNDARAM R, LAKSHMANAN GA and PANNEERSELVAM R. 2007. Growth, biochemical modifications and proline metabolism in Helianthus annuus L. as induced by drought stress. Colloids Surf B Biointerfaces 59: 141-149.
  • MARSCHNER H, KIRKBY EA and CAKMAK I. 1996. Effect of mineral nutritional status on shoot-root partitioning of photoassimilates and cycling of mineral nutrients. J Exp Bot 47: 1255-1263.
  • MEIRA MR, MELO MTP, MARTINS ER, PINTO MJS and SANTANA CS. 2013. Crescimento vegetativo, produção de fitomassa e de óleo essencial de Melissa officinalis L. sob diferentes lâminas de irrigação. Cienc Rural 43: 779-785.
  • MISRA A and SRIVASTAVA NK. 2000. Influence of water stress on Japanese mint. J Herbs Spices Med Plants 7: 51-58.
  • MOHAMMADHOSSEINI M, SARKER SD and AKBARZADEH A. 2017. Chemical composition of the essential oils and extracts of Achillea species and their biological activities: A review. J Ethnopharmacol 199: 257-315
  • NETTO SP and RAFFAELLI G. 2004. Produção experimental de mil-folhas (Achillea millefolium L.), visando à extração de óleo essencial. Rev Acad: Cien Agrarias Amb 2: 27-31.
  • NIST - NATIONAL INSTITUTE OF STANDARDS and TECHNOLOGY. 2008. Topic detection and tracking evaluation. Online. Avaiable at: < http://webbook.nist.gov/chemistry>. (Access in Feb 15, 2015).
    » http://webbook.nist.gov/chemistry>.
  • PEÑUELAS J and LLUSIÀ J. 2002. Linking photorespiration, monoterpenes and thermotolerance in Quercus. New Phytologist 155: 227-237.
  • PEUKE AD. 2010. Correlations in concentrations, xylem and phloem flows, and partitioning of elements and ions in intact plants. J Exp Bot 61: 635-655.
  • PINTO DA, MANTOVANI EC, MELO EDC, SEDIYAMA GC and VIEIRA GHS 2014b. Produtividade e qualidade do óleo essencial de capim-limão (Cymbopogon citratus, DC.) submetido a diferentes lâminas de irrigação. Rev Bras Plant Med 16: 54-61.
  • PINTO JEBP, FERRAZ EO, BERTOLUCCI SKV, SILVEIRA HR, SANTOS AR and SILVA GM. 2014a. Biomass production and essential oil in yarrow cultivated under colored screen types. Hort Bras 32: 321-326.
  • PRAVUSCHI PR, MARQUES PAA, RIGOLIN BHM and SANTOS ACP. 2010. Efeito de diferentes lâminas de irrigação na produção de óleo essencial do manjericão (Ocimum basilicum L.) Acta Sci, Agron 32: 687-693.
  • REDDY AR, CHAITANYA KV and VIVEKANANDAN M. 2004. Drought-induced responses of photosynthesis and antioxidant metabolism in higher plants. J Plant Physiol 161: 1189-1202.
  • REZENDE ME, JASMIM JM, CAPRINI GP, SOUSA EF, SCHRIPSEMA J and THIÉBAUT JTL. 2011. Teor e composição química do óleo essencial de alpínia em razão da adubação e da disponibilidade de água no solo. Rev Ceres 58: 208-215.
  • SILVA SR, DEMUNER AJ, ALMEIDA BARBOSA LC, CASALI VWD, NASCIMENTO EA and PINHEIRO AL. 2012. Efeito do estresse hídrico sobre características de crescimento e a produção de óleo essencial de Melaleuca alternifolia Cheel. Acta Sci 24: 1363-1368.
  • VAN DEN DOOL H and KRATZ PDJA. 1963. Generalization of the retention index system including linear temperature programmed gas-liquid partition chromatography. J Chromat 11: 463-471.

Publication Dates

  • Publication in this collection
    01 Nov 2018
  • Date of issue
    Oct-Dec 2018

History

  • Received
    29 Jan 2018
  • Accepted
    11 July 2018
Academia Brasileira de Ciências Rua Anfilófio de Carvalho, 29, 3º andar, 20030-060 Rio de Janeiro RJ Brasil, Tel: +55 21 3907-8100 - Rio de Janeiro - RJ - Brazil
E-mail: aabc@abc.org.br