• Nu S-Au Găsit Rezultate

View of Growth Parameters and Photosynthetic Pigments of Marigold under Stress Induced by Jasmonic Acid

N/A
N/A
Protected

Academic year: 2022

Share "View of Growth Parameters and Photosynthetic Pigments of Marigold under Stress Induced by Jasmonic Acid"

Copied!
5
0
0

Text complet

(1)

Growth Parameters and Photosynthetic Pigments of Marigold under Stress Induced by Jasmonic Acid

Nilofar ATAEI, Hossein MORADI, Vahid AKBARPOUR*

Department of Horticultural Sciences, Sari Agricultural Sciences and Natural Resources University, Sari, Iran; [email protected] (*corresponding author)

Abstract

In this research, the effects of different concentrations of jasmonic acid ( JA) on growth parameters of flower diameter, number of flowers, dry flower weight, plant height, 1000-seed weight and also, photosynthetic pigments in marigold (Calendula officinalis L.) were investigated. To achieve this aim, marigold planted in pots and jasmonic acid were sprayed on the shoots at concentrations of 0.75, 150 and 225 µM. Data were compared by Duncan test. The results showed that different concentrations of jasmonic acid significantly affected the dry flower weight, plant height and 1000-seed weight. The maximum plant height and 1000-seed weight were reached by 150 µM jasmonic acid, while 225 µM was recorded the dry flower weight.

Keywords: jasmonic acid, marigold, medicinal plants, morphological, phytochemical

Introduction

Marigold (Calendula officialis L.) is an annual plant be- longing to the Asteraceae family, which often it is used as an ornamental and medicinal plant (Chalchat et al., 1991).

According to Dorwal (2012), this plant contains impor- tant compounds such as saponins, flavonoids, carotenoids, xanthophylls, essential oils, mucilage and phenolic acids.

Because of diverse sources of biological activities such as anti-inflammatory and anti-spasmodic effects, mari- gold is used. Also, it is used in gastric disease, eye and skin damage and some burns (Chakraborthy and Ghorpade, 2010).

Jasmonic acid is a plant growth regulator that plays key roles in plant growth and development, and responses to environmental stress (Creelman et al., 1997; Kozlowski et al., 1995). Studies on different plants showed that foliar application of Jasmonic acid increased growth of arabi- dopsis, and tomato compared with control plants (Bough- ton et al., 2005; Devoto and Turner, 2005; Traw and Ber- gelson, 2003).

Baldi and Dixit (2007) also stated that the use of meth- yl jasmonate in plants as elicitor on artemisia increased biomass. Moreover, several reports on the positive effect of Jasmonic acid on increasing the growth of shoots and number of flowers in Phaseolus lunatus and improving flowering in Lemna minor were mentioned (Heil, 2004;

Krajncic et al., 2006).

As Sorial et al., (2010) found in their research, number of stalk, leaf dry weight, shoot dry weight and chlorophyll content in basil plants are increased under treatment of this hormone.

Swiatek et al. (2003) found that jasmonic acid is effec- tive on cell size and cell division.

Ding et al. (2002) stated that low concentrations of methyl jasmonate significantly increased plant resistance and thus it improves growth. The present reports indi- cate that jasmonates are necessary to promote flowers and sexual development in plants. Therefore, in the presence of jasmonate may have occurred early flower development and caused enhancement in production cycles and then increasing flower yield (Delker et al., 2006).

Considering Jasmonic acids as growth regulator ef- fective on phytochemical, and morphological attributes, and since these attributes are directly or indirectly effec- tive on the medicinal properties of marigold, therefore, the purpose of the experiment design is to find some rela- tions between the effects of hormonal treatments and phy- tochemical and morphological changes to achieve optimal effective concentration on desired traits.

Material and methods

To perform this experiment, Jasmonic acid purchased from Sigma (J2500) and the seeds of marigold were ob- tained from the Pakan Bazr Company. The experiment was completely randomized design with four levels of hor- Received 28 July 2013; accepted 07 November 2013

(2)

number (24). There was no statistically difference between different treatments different treatments (p≤0.05).

Fig. 2. Effect of different concentration of jasmonic acid on number of flower

Plants treated with 225 µM jasmonic acid caused the highest flower dry weight (0.44 g) that had no significant difference (p≤0.05) with control plants and plants treated with 150 µM, whereas significant difference (p≤0.05) is observed between this level and the plants treated with 75 µM jasmonic acid (Fig. 3).

Fig. 3. Effect of different concentration of jasmonic acid on dry flower weight

Plant height has a ascending trend from control up to 150 µM. As the highest value of plant height (34.36 cm) was obtained in plants treated with 150 µM that have a significant difference (p≤0.05) with control plant (29.18 cm) (Fig. 4).

Fig. 4. Effect of different concentration of jasmonic acid on plant height

mone including concentrations of 0, 75, 150 and 225 µM jasmonic acid.

Each treatment has 15 replicates. 4-5 leaf stage seed- lings from seeds, transferred in pots filled with peat, leaves soil, potting soil. Plants were sprayed three times with hor- mone. Traits such as flower diameter, number of flowers, dry flower weight, plant height, 1000 seed weight, carote- noids, chlorophyll a and b were examined in this present study. Measurement of chlorophyll and carotenoids was performed by Porra (2002) method.

After the reaction between fresh leaf tissue and metha- nol, absorption were measured by spectrophotometer (Model uv-1800 PC) at a wavelength of 665.2 nm for chlorophyll a, 652.4 nm for chlorophyll b and 470 nm for carotenoids. The content of chlorophyll a, b and carote- noids were calculated from the following formula:

Chlorophyll a= (16.72×A665.2)-(9.16×A652.4) Chlorophyll b= (34.09×A652.4)-(15.28×A665.2)

Carotenoid=[(1000×A470)-1.63×Chlorophyll a-(104.96×Chlorophyll b)]/221

After flower harvest, they were weighted by digital scale (model A&D company limiled) and to measure dry weight were dried in oven (model BM120) at 40 °C for 72 h (Omidbaigi, 1997). Analysis of variance, mean compari- son using Duncan’s multiple range test at the five percent level and drawing graph were done by SPSS software.

Results

Mean comparison results indicated that plants treat- ed with 225 µM had dedicated highest flower diameter (5.26 cm). While no significant difference was observed between any of the treatments (p≤0.05) and the lowest flower diameter (5.06 cm) was obtained in plants treated with 150 µM jasmonic acid (Fig. 1).

Fig. 1. Effect of different concentration of jasmonic acid on flower diameter

As it can be seen in Fig. 2, with the increasing of con- centration of jasmonic acid from 0 to 150 µM, the number of flowers has increased through ascending trend. The ap- plication of jasmonic acid at 150 µM produced the highest

(3)

Moisture content (%) has the descending trend from 0 to 225 µM (Tab. 1). Biomass was enhanced with increas- ing concentration of jasmonic acid as in 225 µM the high- est content was obtained (19.52).

In terms of seed weight, the highest value (13.05 g) was obtained at 150 µM jasmonic acid and control plant was recorded the lowest value (10.80 g).

Plants treated with 150 µM had no significant differ- ence with 75 µM. while significant difference is observed between this level with control plants and 225 µM.

Tab. 1. Means comparison of studied attributes in treatment with jasmonic acid

In each column, means with the same letter has no significant difference.

Considering that statistically nonsignificant difference was found between treatments in terms of carotenoids, but the highest carotenoids content (0.91 µg ml-1) was obtained at 75 µM and plants treated with 225 µM were recorded the lowest carotenoids content (0.82 µg ml-1).

According to the results, with the increasing of the concentration of Jasmonic acid, chlorophyll a increased up to 150 µM.

It is remarkable that there was no significant difference between treatments (p≤0.05). However, significant dif- ferences (p≤0.05) between treatments in terms of chloro- phyll b did not exist, but the highest value (1.074 µg ml-1) was obtained at 225 µM and concentration of 75 µM was accounted for the lowest (0.89 µg ml-1) (Tab. 1).

Tab. 2 also indicates that there is significant positive correlation (p ≤0.01) exist between flower diameters, flower dry weight and also between chlorophyll a and car- otenoids. Diameter and flower number have a significant negative correlation (p ≤0.01). It is remarkable that there is significant positive correlation (p≤0.05) between plant height and flower number.

Also, flower dry weight along with moisture content and biomass has significant negative and positive correla- tion (p≤0.05) respectively. In addition, a significant nega- tive correlation (p≤0.05) is observed between chlorophyll b and carotenoids.

Concentra- tion of hormone

(µM)

Moisture (%) Biomass

(g) 1000

seed weight

(gr)

Carotenoid of leaf (µg ml-1)

Chlorophyll

a (µg ml-1) Chlorophyll b (µg ml-1)

0 83.16 a 16.83 a 10.803

b 0.86 a 3.01 a 1.06 a

75 82.90 a 17.09 a 11.9 ab 0.91 a 3.12 a 0.89 a

150 81.11 a 18.88 a 13.05 a 0.90 a 3.26 a 1.07 a

225 80.47 a 19.52 a 11.34 b 0.82 a 2.96 a 1.074 a

Flower diameter (cm)Number of flowersDry flower weight (gr)Plant height (cm)

1000 seed wCarotenoids Chlorophyll Chlorophyll Moisture eight Biomass-1-1-1(µg ml)a (µg ml)b (µg ml)content (gr) Flower diameter (cm)1 Number of flowers- 0.454**1 nsDry flower weight (gr)0.332**-0.1991 nsnsPlant height (cm)-0.2190.285*-0.0911 nsnsns1000 seed weight (gr)-0.2190.1-0.0570.407**1 l-1nsnsnsnsnsCarotenoids (µg m)-0.0610.031-0.0060.1470.2141 -1nsnsnsnsnsChlorophyll a (µg ml)-0.530.056-0.0270.0900.2210.928**1 -1nsnsnsnsnsChlorophyll b (µg ml)0.0690.0250.109-0.219-0.051-0.282*-0.036*1 nsnsnsnsnsnsnsMoisture content0.006-0.125-0.291*-0.0620.0340.091-0.005-0.171 nsnsnsnsnsnsnsBiomass-0.0060.1250.291*0.0620.034-0.0910.0050.17-1**1 ** (p<0.01), * (p<0.05), ns (p>0.05)

Tab. 2. Correlation coefficients between studied attributes of Calendula officinalis in

(4)

It seems that in case of increasing number of flowers, consumer organ increases too. Thus, each flower reaches less carbohydrate and dwindles. Positive correlation be- tween the plant height and the number of flower can be as a result of direct relation between the plant height and the number of nods. When the plant height increases, number of nods increases too. So, more flowers form at nods.

In this connection, it has been reported that jasmonic acid increased the number of nodes and length of inter- node in tissue culture of Vitis vinifera L. (Ravnikar et al., 1990). In general, considering the results of these experi- ments, high concentrations of jasmonic acid are proposed to achieve the desirable traits of ornamental and medici- nal.

References

Baldi V, Dixit VK (2007). Yield enhancement strategies for ar- temisinin production by suspension cultures of Artemisia annua. Bio Technol 99:4609-4614.

Boughton AJ, Hoover K, Felton GW (2005). Methyl jas- monate application induces increased densities of glandular trichomes on tomato, Lycopersicon esculentum. J Chem Ecol 31:2211-2216.

Chakraborthy GS, Ghorpade PM (2010). Determination of quercetin by HPLC in Calendula officinalos Extract. Inter J Pharma Bio Sci 1(1):405-425.

Chalchat JC, Garry RP, Michet A (1991). Chemical Composi- tion of Essential Oil of Calendula officinalis L. (Pot Mari- gold). Flavour Fragr J 6:189-192.

Creelman RA, Mullet JE (1995). Jasmonic acid distribution and action in plants: regulation during development and re- sponse to biotic and abiotic stress. Proc Natl Acad Sci USA 92:4114-4119.

Delker C, Stenzel I, Hause B, Miersch O, Feussner I, Wasternack C (2006). Jasmonate biosynthesis in Arabidopsis thaliana- enzymes, products, regulation. Plant Biol 8(3):297-306.

Devoto A, Turner JG (2005). Jasmonate-regulated Arabidopsis stress signaling network. Physiol Plantarium 123:161-172.

Ding CK, Wang CY, Gross KC, Smith DL (2002). Jasmonate and salicylate induce the expression of pathogenesis-related- protein genes and increase resistance to chilling injury in to- mato fruit. Planta 214:895-901.

Dorwal D (2012). Anthelmintic activity of Methanolic and Ethanolic Leaf Extract of Calendula officinalis. Int J Res Pharm Biomed Sci 3(2):831-833.

Heil M (2004). Induction of two indirect defenses benefits lima bean (Phaseolus lunatus, Fabaceae) in nature. J Ecol 92:527- 536.

Kozlowski G, Buchala A, Metraux JP (1999). Methyl jasmonate protects norwayprotects norwayprotects norway spruce [Picea abies (L.) Karst.] seedlings against Pythium ultimum trow. Physiol Mol Plant Pathol 55:53-58.

Krajncic B, Kristl J, Janzekovic I (2006). Possible role of jas- Discussion

As the results showed, traits such as flower diameter, flower number and flower dry weight in plants treated with 225 µM jasmonic acid reached the highest values.

These results are consistent with those obtained by (Heil, 2004; Krajncic et al., 2006), who stated that jasmonic acid increases flowering in Lemna minor and Phaseolus luna- tus.Wasternack (2006) also outlined that Jasmonic acid has several roles in flowering and this hormone has effects on anther development, female organ development, chemical defence production, color production, and the attraction of pollinators.

Based on the presented results, dry flower weight at the level of 225 µM significantly was increased than 225 µM.

These findings are in accordance with other research- ers who claimed that jamonates improves growth of arabi- dopsis, tomato, artemisia and basil (Baldi and Dixit, 2007;

Boughton et al., 2005; Sorial et al., 2010; Traw and Ber- gelson, 2003).

In this present study, plant height has ascending trend up to 150 µM, and the highest value of it was obtained at 150 µM. In this context, Heil (2004) stated that the shoot the growth of Phaseolus lunatus L. were enhanced by jas- monic acid treatment.

These results could suggest that jasmonic acid protects plants against biotic stress and abiotic stress and enhance their resistance to damages, so it has had a positive impact on the mentioned traits (Devoto and Turner, 2005; Ding et al., 2002).

Moreover, this hormone can promote the growth by effect on cell size and cell division (Sorial et al., 2010; Swi- atek et al., 2003).

Reduction in shoot growth at high concentrations (225 µM) may be due to high concentrations of jasmon- etes which could act as stress and may reduce the absorp- tion of nutrients, that can lead to the reduction of growth (Rossato et al., 2002).

In this regard, Mathew and Sankar (2012) stated that high concentrations of this hormone are associated with plant cell death. According to the results, it is observed that the highest value of chlorophyll a and b were obtained at 150 and 225 µM, respectively.

The findings were consistent with Sorial et al. (2010) who stated that jasmonic acid causes increment in chloro- phyll in basil plant. They found that jasmonic acid treat- ment causes enhancement in the active cytokine (CK) that ultimately increase the chlorophyll pigments.

Saniewski et al. (2010) also expressed that jasmonetes controls ethylene production in plant tissues that seems by controlling ethylene production, and chlorophyll deg- radation is also reduced. In accordance with the obtained results, by increasing the number of flower, diameter was significantly reduced.

(5)

Saniewski M, Puchalski J, Miyamoto K, Oka M, Ueda J (2010).

Methyl jasmonate-induced gum production in tulip bulbs is stimulated by gibberellic acid. J Fruit Ornamental Plant Res 19(2):161-168.

Sorial ME, El-Gamal SM, Gendy AA (2010). Response of sweet basil to jasmonic acid application in relation to different wa- ter supplies. Bio Res 7(1):39-47.

Swiatek A, Azmi A, Witters E, Van-Onckelen H (2003). Stress messengers jasmonic acid and abscisic acid negatively regu- late plant cell cycle. Bulg J Plant Physiol 172-178.

Traw MB, Bergelson J (2003). Interacive effects of jasmonic acid, salicylic acid, and gibberellin on induction of trichomes in Arabidopsis. Plant Physiol 133:1367-1375.

Wasternack C (2006). Oxylipins: biosynthesis, signal transduc- tion and action. In: Plant Hormone Signaling (Hedden P, Thomas SG, Eds.). Blackwell Publishing, Oxford, UK. p.

185-228.

monic acid in the regulation of floral induction, evocation and floral differentiation in Lemna minor L. Plant Physiol Biochem 44:752-758.

Mathew R, Sankar D, (2012). Effect of methyl jasmonate and chitosan on growth characteristics of Ocimum basilicum L., Ocimum sanctum L. and Ocimum gratissimum L. cell suspen- sion cultures. African J Biotechnol 11(21):4759-4766.

Omidbaigi R (1997). Approaches to production and processing of medicinal plants. Tarahanenashr p. 96

Porra R (2002). The chequered history of the development and use of simultaneous equations for the accurate determination of chlorophylls a and b. Photosynthesis Res 73:149-156.

Ravinkar M, Rode J, Gogala N, Benedicic D (1990). Regulation of organogenesis with jasmonic acid. Acta Horti 280:169- 172.

Rossato L, MacDuff JH, Laine P, Deunff EL, Ourry A (2002).

Nitrogen storage and remobilization in Brassica napus L.

during the growth cycle: effects of methyl jasmonate on ni- trate uptake, senescence, growth, and VSP accumulation. J Exper Botany 53:1131-1141.

Referințe

DOCUMENTE SIMILARE

The effects of chemical preservatives such as sodium benzoate, sodium acetate, citric acid and sodium chloride at different concentrations on the microbial counts and pH of mango

In the present study, the effect of nutrient and light stress on growth parameters like shoot height, number of leaves, leaf area and plant biomass were

The experiment was carried out to determine the effects of heat stress on some growth parameters like shoot height, leaf area, fresh weight, dry weight as well as the accumulation

In gaillardia, (Deshmukh et al., 2008) revealed that, significantly maximum vegetative growth viz., plant height, plant spread, diameter of main stem, 50% flowering, diameter

Effect of Salicylic Acid on Alleviating of Electrolyte Leakage and Flower Organ Damage in Apricot ( Prunus armeniaca L. ‘Shahroudi’).. under Artificial

This study investigated the responses of maize (Zea mays L.) and cowpea (Vigna unguiculata L. Walp.) seedlings growth parameters to nitrogen nutritional stress.. This was with a

The effect of daylight, continuous illumination and acid scarification on the seed germination and seedling vegetative growth (epicotyl and hypocotyl lengths,

Selenium at the lowest level (1 mg L -1 ) stimulated spin- ach growth parameters like shoot and root fresh weight, shoot and root dry weight, total dry weight, shoot and