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Cheghaghasemi, Fatemeh, Safari, Hooshmand, Kahrizi, Danial. (1405). Interactive Effects of Organic Manure and Planting Density on Growth, Essential Oil Production, and Chemotype Expression in Iranian Thymus daenensis Čelak. Genotypes Under Dry Farming. سامانه مدیریت نشریات علمی, 15(5), 573-586. doi: 10.22034/jmpb.2026.372562.2171
Fatemeh Cheghaghasemi; Hooshmand Safari; Danial Kahrizi. "Interactive Effects of Organic Manure and Planting Density on Growth, Essential Oil Production, and Chemotype Expression in Iranian Thymus daenensis Čelak. Genotypes Under Dry Farming". سامانه مدیریت نشریات علمی, 15, 5, 1405, 573-586. doi: 10.22034/jmpb.2026.372562.2171
Cheghaghasemi, Fatemeh, Safari, Hooshmand, Kahrizi, Danial. (1405). 'Interactive Effects of Organic Manure and Planting Density on Growth, Essential Oil Production, and Chemotype Expression in Iranian Thymus daenensis Čelak. Genotypes Under Dry Farming', سامانه مدیریت نشریات علمی, 15(5), pp. 573-586. doi: 10.22034/jmpb.2026.372562.2171
Cheghaghasemi, Fatemeh, Safari, Hooshmand, Kahrizi, Danial. Interactive Effects of Organic Manure and Planting Density on Growth, Essential Oil Production, and Chemotype Expression in Iranian Thymus daenensis Čelak. Genotypes Under Dry Farming. سامانه مدیریت نشریات علمی, 1405; 15(5): 573-586. doi: 10.22034/jmpb.2026.372562.2171

Interactive Effects of Organic Manure and Planting Density on Growth, Essential Oil Production, and Chemotype Expression in Iranian Thymus daenensis Čelak. Genotypes Under Dry Farming

Journal of Medicinal Plants and By-products
مقاله 5، دوره 15، شماره 5، آذر و دی 2026، صفحه 573-586    اصل مقاله (2.91 M)
نوع مقاله: Research Article
شناسه دیجیتال (DOI): 10.22034/jmpb.2026.372562.2171
نویسندگان
Fatemeh Cheghaghasemi1؛ Hooshmand Safari2؛ Danial Kahrizi* 3
1Department of Plant Production Engineering and Genetics, Faculty of Agricultural Science and Engineering, Razi University, Kermanshah, Iran
2Department of Forests and Rangelands Research, Kermanshah Agricultural and Natural Resources Research and Education Center, AREEO, Kermanshah, Iran
3Department of Biotechnology, Faculty of Agriculture, Tarbiat Modares University, Tehran, Iran
چکیده
The cultivation of Thymus daenensis, an endemic Iranian medicinal species rich in phenolic monoterpenes, requires optimization under rainfed conditions to ensure sustainability and productivity. This study investigated the interactive effects of organic manure application (0 and 50 t ha⁻¹), planting density (4, 6, and 8 plant/m), and genotype (four distinct genotypes) on biomass production, essential oil (EO) yield, and EO composition in a dry farming system in western Iran. A split-plot factorial experiment (CRBD, three replications) was conducted over the 2021–2022 growing seasons. Results indicated that plant density, genotype, and manure application significantly influenced fresh and dry biomass yields as well as EO yield. The combination of medium planting density (6 plant/m) with manure application generally maximized productivity, yielding up to 16,398 g/m fresh biomass and 7,122 g/m dry biomass. EO concentration was less variable but ranged from 4.30% to 6.07%, while EO yield increased markedly with manure and optimal density, reaching 435.3 Kg/ha. GC and GC–MS analyses identified thymol, carvacrol, γ-terpinene, p-cymene, and α-terpineol as major compounds. Thymol content varied widely (59.66–72.76%) and was highest under low-density, unfertilized conditions. In contrast, monoterpene hydrocarbons such as p-cymene and γ-terpinene increased under manure application and higher densities. Multivariate analyses (PCA, correlation, clustering) revealed a consistent trade-off: agronomic practices that enhanced biomass and EO yield promoted monoterpene-rich oils, whereas resource-limited conditions (low density, no manure) favored the accumulation of high-value phenolic monoterpenes like thymol and carvacrol. Significant genotype × fertilization × density interactions underscored the need for genotype-specific management strategies. We conclude that medium planting density combined with organic manure optimizes biomass and EO yield under rainfed conditions, while lower inputs enhance EO quality by increasing phenolic content. These findings provide a basis for tailoring cultivation practices according to production goals-whether maximizing yield or obtaining phenolic-rich essential oils for pharmaceutical and industrial uses.
کلیدواژه‌ها
Rainfed agriculture؛ Phenolic monoterpenes؛ Biomass allocation؛ Organic fertilization؛ Chemotype plasticity
مراجع
  1. Yousefi B., Sefidkon F., Safari H. Evaluation of Essential Oil in Satureja spicigera (c. Koch) Boiss. in Dry Farming Under the Effect of Different Organic Fertilizers and Plant Densities. International Journal of Horticultural Science and Technology. 2023;10 (3): 319-332. doi: 10.22059/ijhst.2022.344120.568
  2. Yousefi B., Karamian R. Effects of Salicylic Acid on Photosynthetic Pigments, Osmolytes, and Antioxidant Enzyme Activities in White Savory (Satureja mutica Fisch.) Exposed to Various Salt Levels International Journal of Horticultural Science and Technology. 2025; 12 (1): 69-82. doi: 10.22059/ijhst.2024.365136.693
  3. Bonesi M., Loizzo M.R., Acquaviva R., Malfa G.A., Aiello F., Tundis R. Anti-inflammatory and Antioxidant Agents from Salvia Genus (Lamiaceae): An Assessment of the Current State of Knowledge. Anti-Inflammatory & Anti-Allergy Agents in Medicinal Chemistry. 2017; 16 (2): 70-86. doi: 10.2174/1871523016666170502121419
  4. Elansary H.O., Szopa A., Kubica P., Ekiert H., El-Ansary D.O., Al-Mana F.A., Mahmoud E.A. Saudi Rosmarinus officinalis and Ocimum basilicum L. polyphenols and biological activities. Processes. 2020; 8(4): 446. doi:
  5. Mamadalieva N.Z., Akramov D.K., Böhmdorfer S., Azimova S.S., Rosenau T. Extractives and biological activities of Lamiaceae species growing in Uzbekistan. Holzforschung. 2020; 74(2): 96-115.
  6. Süntar I., Nabavi S.M., Barreca D., Fischer N., Efferth T. Pharmacological and chemical features of Nepeta L. genus: Its importance as a therapeutic agent. Phytotherapy Research. 2018; 32(2): 185-198. doi: 10.1002/ptr.5946
  7. Nieto G. A Review on Applications and Uses of Thymus in the Food Industry. Plants. 2020; 9(8): 961.
  8. Gago C., Serralheiro A., Miguel M.d.G. Anti-Inflammatory Activity of Thymol and Thymol-Rich Essential Oils: Mechanisms, Applications, and Recent Findings. Molecules. 2025; 30(11): 2450.
  9. Vassiliou E., Awoleye O., Davis A., Mishra S. Anti-Inflammatory and Antimicrobial Properties of Thyme Oil and Its Main Constituents. International Journal of Molecular Sciences. 2023; 24: 6936. doi: 10.3390/ijms24086936
  10. Nagoor Meeran M.F., Javed H., Al Taee H., Azimullah S., Ojha S.K. Pharmacological Properties and Molecular Mechanisms of Thymol: Prospects for Its Therapeutic Potential and Pharmaceutical Development. Frontiers in Pharmacology. 2017; 8:2017. doi: 10.3389/fphar.2017.00380
  11. Dong Y., Wei Z., Yang R., Zhang Y., Sun M., Bai H., Mo M., Yao C., Li H., Shi L. Chemical Compositions of Essential Oil Extracted from Eight Thyme Species and Potential Biological Functions. Plants. 2023;12(24): 4164.
  12. Şener İ., TekelİOĞLu F., Zurnacı M., Baloglu P., Gür M., Güney K. Chemical Composition, Antibacterial and Antioxidant Activities of Thymus Praecox. Kastamonu Üniversitesi Orman Fakültesi Dergisi. 2021;21: 65-73. doi: 10.17475/kastorman.908659
  13. Borugă O., Jianu C., Mişcă C., Goleţ I., Gruia A.T., Horhat F.G. Thymus vulgaris essential oil: chemical composition and antimicrobial activity. Journal of Medicine and Life. 2014; 7 Spec No. 3(Spec Iss 3): 56-60.
  14. Raal A., Paaver U., Arak E., Orav A. Content and composition of the essential oil of Thymus serpyllum L. growing wild in Estonia. Medicina (Kaunas). 2004; 40(8): 795-800.
  15. Goharrostami M., Sendi J.J., Hosseini R., Allah Mahmoodi NO. Effect of thyme essential oil and its two components on toxicity and some physiological parameters in mulberry pyralid Glyphodes pyloalis Walker. Pesticide Biochemistry and Physiology. 2022; 188: 105220. doi: 10.1016/j.pestbp.2022.105220
  16. Yang J., Shen G., Wang X., Carmona C.P. Competition-Induced Trait Variability Obscures Trait–Growth Relationships of Tree Seedlings. Ecology Letters. 2025; 28(11): e70259. doi: https://doi.org/10.1111/ele.70259
  17. Baio F.H.R., Oliveira J.T.d., Cunha F.F.d., Teodoro P.E., Teodoro L.P.R., Campos C.N.S., Gava R., Junior J.C.N.A., Alves M.E.M., Ganassim F. Rethinking Variable Rate Seeding: Why Can Increasing Soybean Population Decrease Yield in Nutrient-Limited Soils? Crops. 2025; 5(6): 78.
  18. Yang X-z., Zhang W-h., He Q-y. Effects of intraspecific competition on growth, architecture and biomass allocation of Quercus Liaotungensis. Journal of Plant Interactions. 2019; 14: 284-294. doi: 10.1080/17429145.2019.1629656
  19. Zhang Y., Xu Z., Li J., Wang R. Optimum Planting Density Improves Resource Use Efficiency and Yield Stability of Rainfed Maize in Semiarid Climate. Frontiers in Plant Science Volume. 2019; 12:2021. doi: 10.3389/fpls.2021.752606
  20. Wang R., Wu W., Cheng X., Peng W. High plant density increases sunlight interception and yield of direct-seeded winter canola in China. Experimental Agriculture. 2023; 59: e2. doi: 10.1017/S0014479722000564
  21. Alipour Abookheili F., Mobasser H.R. Effect of planting density on growth characteristics and grain yield increase in successive cultivations of two rice cultivars. Agrosystems, Geosciences & Environment. 2021; 4(4): e20213. doi: https://doi.org/10.1002/agg2.20213
  22. Djalovic I., Prasad P.V.V., Dunđerski D., Katanski S., Latković D., Kolarić L. Optimal Plant Density Is Key for Maximizing Maize Yield in Calcareous Soil of the South Pannonian Basin. Plants. 2024; 13(13): 1799.
  23. Yousefi B., Saed-Moucheshi A., Gheitury M. Interactions of Organic Fertilizers and Planting Densities on Essential Oil and Plant Yield of Satureja mutica in Dry Farming International Journal of Horticultural Science and Technology. 2024; 11(2): 175-188. doi: 10.22059/ijhst.2023.356067.622
  24. Yousefi B., Safari H. Evaluation of Essential Oil, Morphological Traits and Crop Yield in Satureja mutica Fisch. & C. A. Mey. in Rainfed Cultivation under Different Row Spacing Agrotechniques in Industrial Crops. 2022; 2(4): 187-197. doi: 10.22126/atic.2023.8424.1074
  25. Xing Y., Xie Y., Wang X. Enhancing soil health through balanced fertilization: a pathway to sustainable agriculture and food security. Front Microbiol. 2025; 16: 1536524. doi: 10.3389/fmicb.2025.1536524
  26. Prakash O. Excessive use of chemical fertilizers, reduce the fertility power of the soil. 2023.
  27. Cui Z., Yan B., Gao Y., Wu B., Wang Y., Wang H., Xu P., Zhao B., Cao Z., Zhang Y., Xie Y., Hu Y., Ma X., Niu J. Agronomic cultivation measures on productivity of oilseed flax: A review. Oil Crop Science. 2022; 7(1): 53-62. doi: https://doi.org/10.1016/j.ocsci.2022.02.006
  28. Wei X., Xie B., Wan C., Song R., Zhong W., Xin S., Song K. Enhancing Soil Health and Plant Growth through Microbial Fertilizers: Mechanisms, Benefits, and Sustainable Agricultural Practices. Agronomy. 2024; 14(3): 609.
  29. Mandal S., Anand U., López-Bucio J., Radha Kumar M., Lal M.K., Tiwari R.K., Dey A. Biostimulants and environmental stress mitigation in crops: A novel and emerging approach for agricultural sustainability under climate change. Environmental Research. 2023; 233: 116357. doi: https://doi.org/10.1016/j.envres.2023.116357
  30. Galindo F.S., Moreira A., Moraes L.A.C., Teixeira Filho M.C.M., Jalal A., Oliveira C.E.S., Al-Babili S., Pagliari P.H. Chapter Three - Challenges and promising opportunities for biostimulants application in sustainable agriculture. In: Sparks DL (ed) Advances in Agronomy, vol 193. Academic Press. 2025;147-226. doi:https://doi.org/10.1016/bs.agron.2025.05.003
  31. Di Sario L., Boeri P., Matus J.T., Pizzio G.A. Plant Biostimulants to Enhance Abiotic Stress Resilience in Crops. International Journal of Molecular Sciences. 2025; 26 (3): 1129.
  32. Liu H-w., Zhang X-k., Zhang G-z., Kou X-c., Liang W-j. Partial organic substitution weakens the negative effect of chemical fertilizer on soil micro-food webs. Journal of Integrative Agriculture. 2022; 21 (10): 3037-3050. doi: https://doi.org/10.1016/j.jia.2022.07.043
  33. Badagliacca G., Testa G., La Malfa S.G., Cafaro V., Lo Presti E., Monti M. Organic Fertilizers and Bio-Waste for Sustainable Soil Management to Support Crops and Control Greenhouse Gas Emissions in Mediterranean Agroecosystems: A Review. Horticulturae. 2024; 10(5): 427.
  34. Khan M.T., Aleinikovienė J., Butkevičienė L-M. Innovative Organic Fertilizers and Cover Crops: Perspectives for Sustainable Agriculture in the Era of Climate Change and Organic Agriculture. Agronomy. 2024;14(12): 2871.
  35. Bhatia T., Sindhu S.S. Sustainable management of organic agricultural wastes: contributions in nutrients availability, pollution mitigation and crop production. Discover Agriculture. 2024;2(1): 130. doi: 10.1007/s44279-024-00147-7
  36. Ali A., Jabeen N., Chachar Z., Chachar S., Ahmed S., Ahmed N., Laghari A.A., Sahito Z.A., Farruhbek R., Yang Z. The role of biochar in enhancing soil health & interactions with rhizosphere properties and enzyme activities in organic fertilizer substitution. Frontiers in Plant Science. 2025;16:2025. doi: 10.3389/fpls.2025.1595208
  37. Loss A., Couto R., Brunetto G., da Veiga M., Toselli M., Baldi E. Animal manure as fertilizer: changes in soil attributes, productity and food composition. International Journal of Research – granthaalayah. 2019; 7: 307-331. doi: 10.29121/granthaalayah.v7.i9.2019.615
  38. Adekiya A.O., Ejue W.S., Olayanju A., Dunsin O., Aboyeji C.M., Aremu C., Adegbite K., Akinpelu O. Different organic manure sources and NPK fertilizer on soil chemical properties, growth, yield and quality of okra. Scientific Reports. 2020;10(1): 16083. doi: 10.1038/s41598-020-73291-x
  39. Palupi N., Kesumaningwati R., Subeki S., Mujiono K., Sofian S., Paramita S., Arung E. The use of animal manure for improving chemical properties of degraded Ultisol, yield, and secondary metabolic of Zingiber montanum. Journal of Degraded and Mining Lands Management. 2023; 11: 4847. doi: 10.15243/jdmlm.2023.111.4847
  40. Rayne N., Aula L. Livestock Manure and the Impacts on Soil Health: A Review. Soil Systems. 2020; 4(4): 64.
  41. Hua W., Luo P., An N., Cai F., Zhang S., Chen K., Yang J., Han X. Manure application increased crop yields by promoting nitrogen use efficiency in the soils of 40-year soybean-maize rotation. Scientific Reports. 2020; 10 (1): 14882. doi: 10.1038/s41598-020-71932-9
  42. Arpanahi A.A., Feizian M. Arbuscular mycorrhizae alleviate mild to moderate water stress and improve essential oil yield in thyme. Rhizosphere. 2019;9:93-96.
  43. Ansari S., Azarmehr N., Barmoudeh Z., Moslemi Z., Ghahremani H., Mirzaei A., Salehpour Z., Rabani M.R., Doustimotlagh A.H. Evaluation of the protective potential of hydroalcoholic extract of Thymus daenensis on acetaminophen-induced nephrotoxicity in rats. Heliyon. 2020;6(5).
  44. Zarshenas M.M., Krenn L. A critical overview on Thymus daenensis Celak.: phytochemical and pharmacological investigations. Journal of integrative medicine. 2015; 13: 91-98. doi: 10.1016/S2095-4964(15)60166-2
  45. Ghasemi Pirbalouti A., Karimi A., Saidyousefi M., Enteshari S., Golparvar A.R. Diversity of Thymus daenensis Celak in Central and West of Iran. Journal of Medicinal Plant Research 5. 2011.
  46. Emami Bistgani Z., Sefidkon F. Review on ethnobotany, phytochemical, molecular and pharmacological activity of Thymus daenensis Celak. Biocatalysis and Agricultural Biotechnology. 2019; 22: 101400. doi: https://doi.org/10.1016/j.bcab.2019.101400
  47. Nazari M., Ghasemi-Soloklui A.A, Kordrostami M., Abdel Latef A.A.H. Deciphering the response of medicinal plants to abiotic stressors: A focus on drought and salinity. Plant Stress. 2023; 10: 100255. doi: https://doi.org/10.1016/j.stress.2023.100255
  48. Emami Bistgani Z., Siadat S.A., Bakhshandeh A., Ghasemi Pirbalouti A., Hashemi M. Morpho-physiological and phytochemical traits of (Thymus daenensis Celak.) in response to deficit irrigation and chitosan application. Acta Physiologiae Plantarum. 2017; 39(10): 231. doi: 10.1007/s11738-017-2526-2
  49. Ghasemi Pirbalouti A., Hashemi M., Ghahfarokhi F.T. Essential oil and chemical compositions of wild and cultivated Thymus daenensis Celak and Thymus vulgaris L. Industrial Crops and Products. 2013; 48: 43-48. doi: https://doi.org/10.1016/j.indcrop.2013.04.004
  50. Kovats E. Composition of essential oils: Part 7. Bulgarian oil of rose (Rosa damascena Mill.). Journal of Chromatography A. 1987; 406(1): 185-222.
  51. Rostaei M., Fallah S., Carrubba A., Lorigooini Z. Organic manures enhance biomass and improve content, chemical compounds of essential oil and antioxidant capacity of medicinal plants: A review. Heliyon. 2024; 10 (17): e36693. doi: 10.1016/j.heliyon.2024.e36693
  52. Ramasamy M., Ghosh S., Yadav K., Chitra M., B D., S. A S.K., Karthickraja A. The Role of Organic Farming in Enhancing Soil Structure and Crop Performance: A Comprehensive Review. Journal of Scientific Research and Reports. 2024; 30: 890-904. doi: 10.9734/jsrr/2024/v30i102511
  53. Baniyaghoub M., Mozafari H., Karimzadeh K., Rajabzadeh F., Azimi R. The Changes in Yield and Chemical Profile of Essential Oil and Leaf Minerals of Satureja macrantha C.A.Mey. Under Combined Manure and NPK Fertilizer. Journal of Medicinal plants and By-products. 2021; 10(2): 141-148. doi: 10.22092/jmpb.2020.352210.1274
  54. Jadhav V., Grondona T., Pistillo A., Pennisi G., Ghio M., Gianquinto G., Orsini F. Optimizing Planting Density for Increased Resource Use Efficiency in Baby-Leaf Production of Lettuce (Lactuca sativa L.) and Basil (Ocimum basilicum L.) in Vertical Farms. Horticulturae. 2025; 11 (4): 343.
  55. Yadete E., Worku M., Nego J. The optimum plant density for the offseason hybrid maize production in the hot-submoist tropical environment of southwestern Ethiopia can differ from the rainy-season. Agrosystems, Geosciences & Environment. 2025; 8(4): e70275. doi: https://doi.org/10.1002/agg2.70275
  56. Monson R., Trowbridge A., Lindroth R., Lerdau M. Coordinated resource allocation to plant growth–defense tradeoffs. New Phytologist. 2021; 233. doi: 10.1111/nph.17773
  57. Huot B., Yao J., Montgomery B.L., He S.Y. Growth–Defense Tradeoffs in Plants: A Balancing Act to Optimize Fitness. Molecular Plant. 2014; 7(8): 1267-1287. doi: https://doi.org/10.1093/mp/ssu049
  58. Cheng R., Yang S., Wang D., Qin F., Wang S., Meng S. Advances in the Biosynthesis of Plant Terpenoids: Models, Mechanisms, and Applications. Plants (Basel). 2025; 14 (10). doi: 10.3390/plants14101428
  59. Zrimec J., Correa S., Zagorščak M., Petek M., Bleker C., Stare K., Schuy C., Sonnewald S., Gruden K., Nikoloski Z. Evaluating plant growth-defence trade-offs by modelling the interaction between primary and secondary metabolism. bioRxiv: 2024.2009.2015.613124. 2025. doi: 10.1101/2024.09.15.613124
  60. Caretto S., Linsalata V., Colella G., Mita G., Lattanzio V. Carbon Fluxes between Primary Metabolism and Phenolic Pathway in Plant Tissues under Stress. International Journal of Molecular Sciences. 2015; 16(11): 26378-26394. doi: 10.3390/ijms161125967

 

  1. Kumari A., Cruz A., Dhiman P., Impa S.M., Tuinstra M.R., Patil G.B., Jagadish S.V.K. Phenylpropanoid derived flavonoid biosynthesis pathway compensates for abiotic and biotic stress tolerance in dhurrin-free forage sorghum. Environmental and Experimental Botany. 2025; 238: 106230. doi: https://doi.org/10.1016/j.envexpbot.2025.106230
  2. Martínez-Chávez L.A., Hernández-Ramírez M.Y., Feregrino-Pérez A.A., Esquivel Escalante K. Cutting-Edge Strategies to Enhance Bioactive Compound Production in Plants: Potential Value of Integration of Elicitation, Metabolic Engineering, and Green Nanotechnology. Agronomy. 2024; 14(12): 2822.
  3. Gago C., Serralheiro A., Miguel M.D. Anti-Inflammatory Activity of Thymol and Thymol-Rich Essential Oils: Mechanisms, Applications, and Recent Findings. Molecules. 2025; 30 (11): 2450. doi: 10.3390/molecules30112450
  4. Süntar I., Nabavi S.M., Barreca D., Fischer N., Efferth T. Pharmacological and chemical features of Nepeta L. genus: Its importance as a therapeutic agent. Phytotherapy Research. 2018; 32 (2): 185-198. doi: https://doi.org/10.1002/ptr.5946
  5. Gohr S., Liao P., Crocoll C., Boachon B., Förster C., Leidecker F., Wiese N., Zhao D., Wood J., Buell C., Gershenzon J., Dudareva N., Degenhardt J. The biosynthesis of thymol, carvacrol, and thymohydroquinone in Lamiaceae proceeds via cytochrome P450s and a short-chain dehydrogenase. Proceedings of the National Academy of Sciences. 2021; 118: e2110092118. doi: 10.1073/pnas.2110092118
  6. Noman A.M., Sultan M.T., Zafar S., Maaz M., Mazhar A., Hussain M., Imran M., Mujtaba A., Hussain M.T., Alsagaby S.A., Al Abdulmonem W., Khan M.A., Al Jbawi E. Thymol and Carvacrol: Molecular Mechanisms, Therapeutic Potential, and Synergy With Conventional Therapies in Cancer Management. Food Science Nutrition. 2025; 13 (9): e70936. doi: 10.1002/fsn3.70936
  7. Trindade H., Pedro L.G., Figueiredo A.C., Barroso J.G. Chemotypes and terpene synthase genes in Thymus genus: State of the art. Industrial Crops and Products. 2018; 124: 530-547. doi: https://doi.org/10.1016/j.indcrop.2018.08.021
  8. Kianersi F., Pour-Aboughadareh A., Majdi M., Poczai P. Effect of Methyl Jasmonate on Thymol, Carvacrol, Phytochemical Accumulation, and Expression of Key Genes Involved in Thymol/Carvacrol Biosynthetic Pathway in Some Iranian Thyme Species. International Journal of Molecular Sciences. 2021; 22 (20): 11124.
  9. Habibi S., Qaderi A., Fatehi F. The Study of Relative Expression of Key Genes of Thymol Biosynthesis Pathway in Thymus vulgaris cv. ‘Varico 3’ under Cold Stress Using Real-Time PCR. Journal of Medicinal Plants. 2017; 16 (64): 50.
  10. Majdi M., Mashhady A., Maroufi A., Crocoll C. Tissue-specific gene-expression patterns of genes associated with thymol/carvacrol biosynthesis in thyme ( Thymus vulgaris L.) and their differential changes upon treatment with abiotic elicitors. Plant Physiology and Biochemistry. 2017; 115. doi: 10.1016/j.plaphy.2017.03.016
  11. Etri K., Pluhár Z. Exploring Chemical Variability in the Essential Oils of the Thymus Genus. Plants. 2024; 13(10): 1375.
  12. Ouarghidi A., Abbad I., Mfuni T. Factors Shaping Phenotypic Variation in Thymus saturejoides. Plants. 2025; 14 (12): 1772.
  13. Llorens L., Llorens-Molina J.A., Agnello S., Boira H. Geographical and environment-related variations of essential oils in isolated populations of Thymus richardii Pers. in the Mediterranean basin. Biochemical Systematics and Ecology. 2014; 56: 246-254. doi: https://doi.org/10.1016/j.bse.2014.05.007
  14. Zhang X., Ran Q., Han Y., Gan L., Zou X., Dong C. The rhizosphere microecological mechanisms of stress-induced quality enhancement in medicinal plants. Plant Stress. 2025; 17: 100965. doi: https://doi.org/10.1016/j.stress.2025.100965
  15. Abbasi S., Houshmand S., Ghorbani S. Gene expression and metabolite analyses of Thymus daenensis and T.vulgaris in the Trichome and leaf at two phenological stages. Biocatalysis and Agricultural Biotechnology. 2024; 57: 103103. doi: https://doi.org/10.1016/j.bcab.2024.103103
  16. Shan Y., Jin S. Biosynthetic Machinery to Abiotic Stress-Driven Emission: Decoding Multilayer Regulation of Volatile Terpenoids in Plants. Antioxidants. 2025; 14(6): 673.
  17. Sun Y., Alseekh S., Fernie A.R. Plant secondary metabolic responses to global climate change: A meta-analysis in medicinal and aromatic plants. Global Change Biology. 2023; 29(2): 477-504. doi: https://doi.org/10.1111/gcb.16484
  18. Hattas D., Scogings P.F., Julkunen-Tiitto R. Does the Growth Differentiation Balance Hypothesis Explain Allocation to Secondary Metabolites in Combretum apiculatum , an African Savanna Woody Species? Journal of Chemical Ecology. 2017; 43(2): 153-163. doi: 10.1007/s10886-016-0808-6
  19. Qaderi M.M., Martel A.B., Strugnell C.A. Environmental Factors Regulate Plant Secondary Metabolites. Plants (Basel). 2023; 12(3): doi: 10.3390/plants12030447
  20. Ray A., Kundu S., Mohapatra S., Sinha S., Khoshru B., Keswani C., Mitra D. An Insight into the Role of Phenolics in Abiotic Stress Tolerance in Plants: Current Perspective for Sustainable Environment. Journal of Pure and Applied Microbiology. 2024; 18. doi: 10.22207/JPAM.18.1.09
  21. Alami M., Guo S., Mei Z., Yang G., Wang X. Environmental factors on secondary metabolism in medicinal plants: exploring accelerating factors. Medicinal Plant Biology. 2024; 3: 1-11. doi: 10.48130/mpb-0024-0016
  22. Ahlawat Y.K., Singh M., Manorama K., Lakra N., Zaid A., Zulfiqar F. Plant phenolics: neglected secondary metabolites in plant stress tolerance. Brazilian Journal of Botany. 2024; 47(3): 703-721. doi: 10.1007/s40415-023-00949-x
  23. Ali-Arab H., Bahadori F., Mirza M., Badi H.N., Kalate-Jari S. Variability in essential oil composition and phenolic acid profile of Thymus daenensis Celak. populations from Iran. Industrial Crops and Products. 2022; 178: 114345. doi: https://doi.org/10.1016/j.indcrop.2021.114345
  24. Liu Y., Lan X., Hou H., Ji J., Liu X., Lv Z. Multifaceted Ability of Organic Fertilizers to Improve Crop Productivity and Abiotic Stress Tolerance: Review and Perspectives. Agronomy. 2024; 14(6): 1141.
  25. Tohidi B., Rahimmalek M., Arzani A., Trindade H. Sequencing and variation of terpene synthase gene (TPS2) as the major gene in biosynthesis of thymol in different Thymus species. Phytochemistry. 2020; 169: 112126. doi: 10.1016/j.phytochem.2019.112126
  26. Pazouki L., Niinemets Ü. Multi-Substrate Terpene Synthases: Their Occurrence and Physiological Significance. Frontiers in Plant Science. 2016;7:2016. doi: 10.3389/fpls.2016.01019
آمار
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سامانه مدیریت نشریات علمی. طراحی و پیاده سازی از سیناوب