Phenolic profiling unravelling allelopathic encounters in agroecology

[en] Allelopathy, a biological phenomenon involving the production and release of secondary metabolites known as allelochemicals, plays a critical role in plant interactions and agroecosystem dynamics. Phenolic compounds are a significant class of allelochemicals that profoundly affect plant competition, soil health, and microbial communities. When released into the soil, their action depends on the soil's physico-chemical characteristics and microbial communities. This review comprehensively inspects phenolic allelochemicals’ structure-function relationship, their direct combat with root cells in the rhizosphere, ecological functions, and their role in plant succession and stress tolerance. Phenolic allelochemicals, characterized by their diverse structures and ecological roles, offer a sustainable alternative to synthetic herbicides due to their minimal residual impact on the environment and rapid biodegradation. Additionally, the review addresses the challenges and future directions in applying phenolic allelochemicals, aiming to bridge the gap between ecological theory and practical agricultural applications for environmental protection and crop productivity enhancement.

Disciplines :

Agriculture & agronomy
Chemistry

Author, co-author :

Mushtaq, Waseem ; Université de Liège - ULiège > Département GxABT > Chemistry for Sustainable Food and Environmental Systems (CSFES)

Fauconnier, Marie-Laure ; Université de Liège - ULiège > TERRA Research Centre > Chemistry for Sustainable Food and Environmental Systems (CSFES)

Language :

English

Title :

Phenolic profiling unravelling allelopathic encounters in agroecology

Publication date :

June 2024

Journal title :

Plant Stress

eISSN :

2667-064X

Publisher :

Elsevier BV

Pages :

100523

Peer reviewed :

Peer Reviewed verified by ORBi

Additional URL :

https://api.elsevier.com/content/article/PII:S2667064X24001763?httpAccept=text/xml

Funders :

ULiège - Université de Liège [BE]

Available on ORBi :

since 27 June 2024

Statistics

Number of views

18 (5 by ULiège)

Number of downloads

10 (2 by ULiège)

More statistics

Scopus citations^®

Scopus citations^®
without self-citations

OpenAlex citations

Bibliography

Aci, M.M., Sidari, R., Araniti, F., Lupini, A., Emerging trends in allelopathy: A genetic perspective for sustainable agriculture. Agronomy, 12(9), 2022, 2043.
Ain, Q., Mushtaq, W., Shadab, M., Siddiqui, M.B., Allelopathy: an alternative tool for sustainable agriculture. Physiology and Molecular Biology of Plants, 2023, 1–17.
Amb, M.K., Ahluwalia, A.S., Allelopathy: potential role to achieve new milestones in rice cultivation. Rice Science 23:4 (2016), 165–183.
Anwar, S., Naseem, S., Ali, Z., Biochemical analysis, photosynthetic gene (psbA) down-regulation, and in silico receptor prediction in weeds in response to exogenous application of phenolic acids and their analogues. PLoS. One, 18, 2023, e0277146.
Ávila-Román, J., Soliz-Rueda, J.R., Bravo, F.I., Aragonès, G., Suárez, M., Arola-Arnal, A., Mulero, M., Salvadó, M.J., Arola, L., Torres-Fuentes, C., Muguerza, B., Phenolic compounds and biological rhythms: Who takes the lead?. Trends. Food Sci. Technol. 113 (2021), 77–85, 10.1016/j.tifs.2021.04.050.
Basaran, F., Ecological Aspects of Allelopathy. International Journal of Agriculture Forestry and Life Sciences 5:1 (2021), 80–86.
Batish, DR, Kaur, S, Singh, HP, Kohli, RK, Role of root-mediated interactions in phytotoxic interference of Ageratum conyzoides with rice (Oryza sativa). Flora 204:5 (2009), 388–395.
Bertholdsson, N.O., Breeding spring wheat for improved allelopathic potential. Weed. Res. 50:1 (2010), 49–57.
Blum, U, Allelopathy: A soil system perspective. Reigosa, MJ, Pedrol, N, González, L, (eds.) Allelopathy: a Physiological Process With Ecological Implications, 2006, Springer, 299–340.
Chai, T.T., Ooh, K.F., Ooi, P.W., Chue, P.S., Wong, F.C., Leucaena leucocephala leachate compromised membrane integrity, respiration and antioxidative defence of water hyacinth leaf tissues. Bot. Stud. 54 (2013), 1–7.
Cheema, Z.A., Farooq, M., Khaliq, A., Application of allelopathy in crop production: success story from Pakistan. Allelopathy: current trends and future applications, 2013, 113–143.
Chen, K.J., Zheng, Y.Q., Kong, C.H., Zhang, S.Z., Li, J., Liu, X.G., 2, 4-Dihydroxy-7-methoxy-1, 4-benzoxazin-3-one (DIMBOA) and 6-methoxy-benzoxazolin-2-one (MBOA) levels in the wheat rhizosphere and their effect on the soil microbial community structure. J. Agric. Food Chem. 58:24 (2010), 12710–12716.
Chen, L., Li, J., Zhu, Y., Guo, L., Ji, R., Miao, Y., Liu, D., Caffeic acid, an allelochemical in Artemisia argyi, inhibits weed growth via suppression of mitogen-activated protein kinase signaling pathway and the biosynthesis of gibberellin and phytoalexin. Front. Plant Sci., 12, 2022, 802198.
Chen, Q., Zhu, B., Sun, D., Liu, W., Sun, X., Duan, S., The effect of protocatechuic acid on the phycosphere in harmful algal bloom species Scrippsiella trochoidea. Aquatic Toxicology, 227, 2020, 105591, 10.1016/j.aquatox.2020.105591.
Cheng, F., Cheng, Z., Research progress on the use of plant allelopathy in agriculture and the physiological and ecological mechanisms of allelopathy. Front. Plant Sci., 6, 2015, 1020.
Cheynier, V., Comte, G., Davies, K.M., Lattanzio, V., Martens, S., Plant phenolics: Recent advances on their biosynthesis, genetics, and ecophysiology. Plant Physiology and Biochemistry 72 (2013), 1–20, 10.1016/j.plaphy.2013.05.009.
Chotsaeng, N., Laosinwattana, C., Charoenying, P., Herbicidal activities of some allelochemicals and their synergistic behaviors toward Amaranthus tricolor L. Molecules., 22(11), 2017, 1841.
Chotsaeng, N., Laosinwattana, C., Charoenying, P., Herbicidal Activities of Some Allelochemicals and Their Synergistic Behaviors toward Amaranthus tricolor L. Molecules., 22, 2017, 10.3390/molecules22111841.
Chou, C.H., Yang, C.M., Allelopathic research of subtropical vegetation in Taiwan II. Comparative exclusion of understory by Phyllostachys edulis and Cryptomeria japonica. J. Chem. Ecol. 8 (1982), 1489–1507.
Chowdhary, V., Alooparampil, S., Pandya, R.V., Tank, J.G., Physiological function of phenolic compounds in plant defense system. Phenolic Compounds—Chemistry, Synthesis, Diversity, Non-Conventional Industrial, Pharmaceutical and Therapeutic Applications. IntechOpen, 2021, 10.5772/intechopen.101131 Available at.
Cipollini, D., Rigsby, C.M., Barto, E.K., Microbes as targets and mediators of allelopathy in plants. J. Chem. Ecol. 38 (2012), 714–727.
Clocchiatti, A., Hannula, S.E., van den Berg, M., Hundscheid, M.P.J., de Boer, W., Evaluation of Phenolic Root Exudates as Stimulants of Saptrophic Fungi in the Rhizosphere. Front. Microbiol., 12, 2021.
Commisso, M., Toffali, K., Strazzer, P., Stocchero, M., Ceoldo, S., Baldan, B., Levi, M., Guzzo, F., Impact of phenylpropanoid compounds on heat stress tolerance in carrot cell cultures. Front. Plant Sci. 7 (2016), 1–16.
de Albuquerque, MB, dos Santos, RC, Lima, LM, Filho, PAM, Nogueira, JMC, da Câmara, CAG, Ramos, AR, Allelopathy, an alternative tool to improve cropping systems. A review. Agron. Sustain. Dev. 31 (2011), 379–395, 10.1051/agro/2010031.
de Lima, G.M., de Lima, J.D., de Lima, V.A., Trezzi, M.M., de Noronha Sales, B.H.L., Hendges, A.P.P.K., Menin, M., Teixeira, S.D., Assessment of allelopathic potential of the salicylic acid on target plants: Euphorbia heterophylla and Bidens pilosa. Research, Society and Development, 11, 2022, e6911124863.
Devi, M., Allelopathy in agroforestry: a review. Journal of Pharmacognosy and Phytochemistry 6:3 (2017), 686–688.
Ding, L., Hong, L., Wang, Y.H., Wang, Y.C., Lin, S.X., Li, M.Z., Wang, H.B., Allelopathic effects of soil pH on nitrogen uptake, its utilization efficiency and soil enzymes in tea bush soil. Allelopathy Journal, 56(2), 2022, 181.
Dixit, G., Praveen, A., Tripathi, T., Yadav, V.K., Verma, P.C., Herbivore-responsive cotton phenolics and their impact on insect performance and biochemistry. J. Asia Pac. Entomol. 20:2 (2017), 341–351.
Einhellig, F.A., Interactions involving allelopathy in cropping systems. Agron. J. 88:6 (1996), 886–893.
Etzerodt, T, Nielsen, ST, Mortensen, AG, Christophersen, C, Fomsgaard, IS, Elucidating the transformation pattern of the cereal allelochemical 6-methoxy-2-benzoxazolinone (MBOA) and the trideuteriomethoxy analogue [D3]-MBOA in soil. J Agr Food Chem 54:4 (2006), 1075–1085.
Fadhel, L.Z., AL-Behadili, A.A., Integration of Sunflower and Sorghum Water Extracts Applied Alone or in Combination With Reduced Doses of Chevalier for Weed Control in Wheat. Iraqi Journal of Science, 2023, 10–24996.
Fomsgaard, I.S., Mortensen, A.G., Idinger, J., Coja, T., Blumel, S., Transformation of benzoxazinones and derivatives and microbial activity in the test environment of soil ecotoxicological tests on Poecilus cupreus and Folsomia candida. J. Agric. Food Chem. 54:4 (2006), 1086–1092.
Gao, H., Zhang, Z., Lv, X., Cheng, N., Peng, B., Cao, W., Effect of 24-epibrassinolide on chilling injury of peach fruit in relation to phenolic and proline metabolisms. Postharvest Biology and Technology 111 (2016), 390–397.
Gaudêncio, S.P., Bayram, E., Lukić Bilela, L., Cueto, M., Díaz-Marrero, A.R., Haznedaroglu, B.Z., Tasdemir, D., Advanced Methods for Natural Products Discovery: Bioactivity Screening, Dereplication, Metabolomics Profiling, Genomic Sequencing, Databases and Informatic Tools, and Structure Elucidation. Mar. Drugs, 21(5), 2023, 308.
. &Gavinet, J., Santonja, M., Baldy, V., Hashoum, H., Peano, S., Tchong, T., Bousquet-Mélou, A., Phenolics of the understory shrub Cotinus coggygria influence Mediterranean oak forests diversity and dynamics. For. Ecol. Manage 441 (2019), 262–270.
Gealy, D.R., Yan, W., Weed suppression potential of ‘Rondo'and other indica rice germplasm lines. Weed Technology 26:3 (2012), 517–524.
Ghimire, BK, Ghimire, B, Yu, CY, Chung, IM, Allelopathic and autotoxic effects of Medicago sativa-derived allelochemicals. Plants, 8(7), 2019, 233.
Guerrieri A, Dong L, Bouwmeester HJ (2019) Role and exploitation of underground chemical signaling in plants.
Haig, T., Allelochemicals in plants. Allelopathy in Sustainable Agriculture and Forestry, 2008, Springer New York, New York, NY, 63–104.
Hameed, A, Shahina, M, Young, LS, Lai, WA, Sridhar, KR, Young, CC, Bacteriostatic stimulus of meropenem on allelochemical-metabolizing Burkholderia sp. LS-044 mitigates ferulic acid autotoxicity in rice (Oryza sativa ssp. japonica cv. Tainung 71). Plant Soil., 2019, 1–14.
Hoang Anh, L., Van Quan, N., Tuan Nghia, L., Dang Xuan, T., Phenolic allelochemicals: Achievements, limitations, and prospective approaches in weed management. Weed. Biol. Manage 21:2 (2021), 37–67.
Hu, L., Robert, C.A., Cadot, S., Zhang, X., Ye, M., Li, B., Manzo, D., Chervet, N., Steinger, T., Van Der Heijden, M.G., Root exudate metabolites drive plant-soil feedbacks on growth and defense by shaping the rhizosphere microbiota. Nat. Commun., 9, 2018, 2738.
Hussain, M.I., Reigosa, M.J., Secondary Metabolites, Ferulic Acid and p-Hydroxybenzoic Acid Induced Toxic Effects on Photosynthetic Process in Rumex acetosa L. Biomolecules., 11, 2021, 10.3390/biom11020233.
Jabran, K, Farooq, M, Aziz, T, Siddique, KHM, Allelopathy and crop nutrition. Cheema, ZA, Farooq, M, Wahid, A, (eds.) Allelopathy: Current Trends and Future Applications, 2013, Springer, the Netherlands, 337348.
Jabran, K, Mahajan, G, Sardana, V, Chauhan, BS, Allelopathy for weed control in agricultural systems. CropProt 72 (2015), 57–65.
Jabran, K., Farooq, M., Implications of Potential Allelopathic Crops in Agricultural Systems. Cheema, Z.A., Farooq, M., Wahid, A., (eds.) Allelopathy: Current Trends and Future Applications, 2013, Springer, Berlin, 349–385.
McGivern, B.B., Tfaily, M.M., Borton, M.A., Kosina, S.M., Daly, R.A., Nicora, C.D., Wrighton, K.C., Decrypting bacterial polyphenol metabolism in an anoxic wetland soil. Nat. Commun., 12(1), 2021, 2466.
Li, Jinjin, Huang, Yumei, Chen, L., Gao, S., Zhang, J., Understory plant diversity and phenolic allelochemicals across a range of Eucalyptus grandis plantation ages. J. For. Res. (Harbin) 34 (2023), 1577–1590, 10.1007/s11676-023-01606-5.
Kato-Noguchi, H., Kurniadie, D., Allelopathy and allelochemicals of Leucaena leucocephala as an invasive plant species. Plants, 11(13), 2022, 1672.
Kaur, A., Kaur, S., Singh, H.P., Datta, A., Chauhan, B.S., Ullah, H., Batish, D.R., Ecology, Biology, Environmental Impacts, and Management of an Agro-Environmental Weed Ageratum conyzoides. Plants, 12(12), 2023, 2329.
Kaur, R., Callaway, R.M., Soils and the conditional allelopathic effects of a tropical invader. Soil Biology and Biochemistry 78 (2014), 316–325.
Khatun, M.R., Tojo, S., Teruya, T., Kato-Noguchi, H., Trewia nudiflora Linn, a Medicinal Plant: Allelopathic Potential and Characterization of Bioactive Compounds from Its Leaf Extracts. Horticulturae, 9(8), 2023, 897.
Kiani, R., Arzani, A., Mirmohammady Maibody, S.A.M, Polyphenols, flavonoids, and antioxidant activity involved in salt tolerance in wheat, Aegilops cylindrica and their amphidiploids. Front. Plant Sci., 12, 2021, 646221.
Kiely, C., Randall, N., Kaczorowska-Dolowry, M., The application of allelopathy in integrated pest management systems to control temperate European crop pests: a systematic map. CABI. Agric. Biosci., 4(1), 2023, 42.
Kong, C.H., Chen, X.H., Hu, F., Zhang, S.Z., Breeding of commercially acceptable allelopathic rice cultivars in China. Pest. Manage Sci. 67 (2011), 1100–1106, 10.1002/ps.2154.
Korableva, N.P., Morozova, E.V., Popova, L.V., Metlitskii, L.V., Specific growth inhibitors in connection with dormancy and immunity in plants. Dok. Akad. Nauk SSSR 184 (1969), 979–981.
Kumar, J., Ramlal, A., Kumar, K., Rani, A., Mishra, V., Signaling pathways and downstream effectors of host innate immunity in plants. Int. J. Mol. Sci., 22(16), 2021, 9022.
Kumar, N., Singh, H., Giri, K., Kumar, A., Joshi, A., Yadav, S., Mishra, G., Physiological and molecular insights into the allelopathic effects on agroecosystems under changing environmental conditions. Physiology and Molecular Biology of Plants 30:1 (2024), 417–433.
Kumar, S., Abedin, M.M., Singh, A.K., Das, S., Role of phenolic compounds in plant-defensive mechanisms. Plant Phenolics in Sustainable Agriculture: 1, 2020, 517–532.
Kumar, N., Goel, N., Phenolic acids: Natural versatile molecules with promising therapeutic applications. Biotechnology Reports, 24, 2019, e00370, 10.1016/j.btre.2019.e00370.
Ladhari, A., Gaaliche, B., Zarrelli, A., Ghannem, M., Ben Mimoun, M., Allelopathic potential and phenolic allelochemicals discrepancies in Ficus carica L. cultivars. South African Journal of Botany 130 (2020), 30–44, 10.1016/j.sajb.2019.11.026.
Lambers, H., Chapin, F.S., Pons, T.L., Lambers, H., Chapin, F.S., Pons, T.L., Ecological biochemistry: allelopathy and defense against herbivores. Plant physiological ecology, 2008, 445–477.
Lattanzio, V., Lattanzio, V.M., Cardinali, A., Role of phenolics in the resistance mechanisms of plants against fungal pathogens and insects. Phytochemistry: Advances in research 661:2 (2006), 23–67.
Lee, R.B., Effects of organic acids on the loss of ions from barley roots. J. Exp. Bot. 28:3 (1977), 578–587.
Li, L., Shewry, P.R., Ward, J.L., Phenolic acids in wheat varieties in the HEALTHGRAIN diversity screen. J. Agric. Food Chem. 56:21 (2008), 9732–9739.
Li, Z.H., Wang, Q., Ruan, X., Pan, C.D., Jiang, D.A., Phenolics and plant allelopathy. Molecules. 15:12 (2010), 8933–8952.
Liu, S, Qin, F, Yu, S, Eucalyptus urophylla root-associated fungi can counteract the negative influence of phenolic acid allelochemicals. Appl. Soil. Ecol. 127 (2018), 1–7.
Mahmood, A., Cheema, Z.A., Mushtaq, M.N., Farooq, M., Maize–sorghum intercropping systems for purple nutsedge management. Archives of Agronomy and Soil Science 59:9 (2013), 1279–1288.
Manivel, T., Sandhiya, T., Deepika, S., Selvakumar, S.V., Karnan, T.M., Adeyemi, D.E., Thanapaul, R.J.R.S., Chemical communication between plant roots and microbes within the rhizosphere. Plant-Microbe Interaction-Recent Advances in Molecular and Biochemical Approaches, 2023, 141–164.
Maqbool, N., Sadiq, R., Allelochemicals as growth stimulators for drought stressed maize. Am. J. Plant Sci. 8:5 (2017), 985–997.
Marchiosi, R., dos Santos, W.D., Constantin, R.P., de Lima, R.B., Soares, A.R., Finger-Teixeira, A., Ferrarese-Filho, O., Biosynthesis and metabolic actions of simple phenolic acids in plants. Phytochemistry Reviews 19 (2020), 865–906.
Mehdizadeh, M., Mushtaq, W., Chapter 9 - Biological Control of Weeds by Allelopathic Compounds From Different Plants: A BioHerbicide Approach. Egbuna, C., Sawicka, B., (eds.) Natural Remedies for Pest, Disease and Weed Control, 2020, Academic Press, 107–117, 10.1016/B978-0-12-819304-4.00009-9.
Meksawat, S., Pornprom, T., Allelopathic effect of itchgrass (Rottboellia cochinchinensis) on seed germination and plant growth. Weed. Biol. Manage 10:1 (2010), 16–24.
Misra, D., Dutta, W., Jha, G., Ray, P., Interactions and Regulatory Functions of Phenolics in Soil-Plant-Climate Nexus. Agronomy, 13(2), 2023, 280, 10.3390/agronomy13020280.
Mushtaq, W, Ain, Q, Siddiqui, MB, Screening of allelopathic activity of the leaves of Nicotiana plumbaginifolia Viv. on some selected crops in Aligarh, Uttar Pradesh, India. Int J Photochem Photobiol 2:1 (2018), 1–4.
Mushtaq, W., Ain, Q., Siddiqui, M.B., Alharby, H.F., Hakeem, K.R., Interspecific Inhibitory Interference of Nicotiana plumbaginifolia Viv. on Pisum sativum L. J. Plant Growth Regul. 40 (2021), 2037–2048.
Mushtaq, W., Fauconnier, M.L., De Clerck, C., Assessment of induced allelopathy in crop-weed co-culture with rye-pigweed model. Sci. Rep., 14(1), 2024, 10446.
Mushtaq, W., Mehdizade, M., Siddiqui, M.B., Ozturk, M., Jabran, K., Altay, V., Phytotoxicity of above-ground weed residue against some crops and weeds. Pak J Bot 52:3 (2020), 851–860.
Mushtaq, W., Siddiqui, M.B., Hakeem, K.R., Allelopathy Potential of Important Crops. Allelopathy: Potential for Green Agriculture, 2020, 25–35.
Mushtaq, W., Siddiqui, M.B., Hakeem, K.R., Allelopathic control of native weeds. Allelopathy: Potential for Green Agriculture, 2020, 53–59.
Mushtaq, W., Ain, Q., Siddiqui, M.B., Alharby, H., Hakeem, K.R., Allelochemicals change macromolecular content of some selected weeds. South African journal of botany 130 (2020), 177–184.
na-Bednarz, M., Płonka, J., Barchanska, H., Allelopathy as a source of bioherbicides: challenges and prospects for sustainable agriculture. Reviews in Environmental Science and Bio/Technology, 2023, 1–34.
Naikoo, M.I., Dar, M.I., Raghib, F., Jaleel, H., Ahmad, B., Raina, A., Naushin, F., Plant signaling molecules. Chapter 9 (2019), 157–168.
Okumu, OO, Muthomi, JW, Ojiem, J, Narla, R, Nderitu, JH, Effect of legume extracts on germination, seedling health of beans (Phaseolus vulgaris L.) and soil microorganisms. Int. J. Plant Soil. Sci., 2019, 1–13.
Oppenheimer-Shaanan, Y., Jakoby, G., Starr, M.L., Karliner, R., Eilon, G., Itkin, M., Malitsky, S., Klein, T., A dynamic rhizosphere interplay between tree roots and soil bacteria under drought stress. Elife, 11, 2022, e79679, 10.7554/eLife.79679.
Pan, L., He, F., Liang, Q., Bo, Y., Lin, X., Javed, Q., Ullah, M.S., Sun, J., Allelopathic Effects of Caffeic Acid and Its Derivatives on Seed Germination and Growth Competitiveness of Native Plants (Lantana indica) and Invasive Plants (Solidago canadensis). Agriculture, 13(9), 1719, 2023, 10.3390/agriculture13091719.
Pardo-Muras, M., Puig, C.G., Pedrol, N., Complex synergistic interactions among volatile and phenolic compounds underlie the effectiveness of allelopathic residues added to the soil for weed control. Plants, 11(9), 2022, 1114.
Politycka, B., Free and glucosylated phenolics, phenol β-glucosyltransferase activity and membrane permeability in cucumber roots affected by derivatives of cinnamic and benzoic acids. Acta Physiologiae Plantarum 19 (1997), 311–317.
Pompeu, DR, Larondelle, Y, Rogez, H, Abbas, O, Pierna, JAF, Baeten, V, Characterization and discrimination of phenolic compounds using Fourier transform Raman spectroscopy and chemometric tools. BASE 22:1 (2018), 13–28.
Potter, M.J., Vanstone, V.A., Davies, K.A., Kirkegaard, J.A., Rathjen, A.J., Reduced susceptibility of Brassica napus to Pratylenchus neglectus in plants with elevated root levels of 2-phenylethyl glucosinolate. J. Nematol., 31(3), 1999, 291.
Pratyusha, S., Phenolic compounds in the plant development and defense: an overview. Plant stress physiology-perspectives in agriculture, 2022, 125–140.
Quan, N.V., Xuan, T.D., Tran, H.D., Thuy, N.T.D., Inhibitory activities of momilactones A, B, E, and 7-ketostigmasterol isolated from rice husk on paddy and invasive weeds. Plants, 8(6), 2019, 159.
Reetu Tomar, M., Kumar, M., Seva Nayak, D., Role of phenolic metabolites in salinity stress management in plants. Plant Phenolics in Abiotic Stress Management, 2023, Singapore: Springer Nature Singapore, 353–368.
Rinschen, M.M., Ivanisevic, J., Giera, M., Siuzdak, G., Identification of bioactive metabolites using activity metabolomics. Nature reviews Molecular cell biology 20:6 (2019), 353–367.
Roleira, FM, Varela, CL, Costa, SC, Tavares-da-Silva, EJ, Phenolic derivatives from medicinal herbs and plant extracts: anticancer effects and synthetic approaches to modulate biological activity. Stud Nat Prod Chem 57 (2018), 115–156.
Safdar, M.E., Aziz, A., Farooq, U., Hayat, M.S., Rehman, A., Qamar, R., Awan, T.H., Germination and growth of some summer crops as affected by allelopathicity of different waste-land weeds. J. Res. Weed Sci 2:4 (2019), 358–371.
Scavo, A., Mauromicale, G., Crop allelopathy for sustainable weed management in agroecosystems: Knowing the present with a view to the future. Agronomy, 11(11), 2021, 2104.
Scavo, A., Abbate, C., Mauromicale, G., Plant allelochemicals: Agronomic, nutritional and ecological relevance in the soil system. Plant Soil. 442 (2019), 23–48.
Serra Serra, N., Shanmuganathan, R., Becker, C., Allelopathy in rice: A story of momilactones, kin recognition, and weed management. J. Exp. Bot. 72:11 (2021), 4022–4037.
Sharma, A., Shahzad, B., Rehman, A., Bhardwaj, R., Landi, M., Zheng, B., Response of phenylpropanoid pathway and the role of polyphenols in plants under abiotic stress. Molecules., 24(13), 2019, 2452.
Singh, A.A., Ghosh, A., Agrawal, M., Agrawal, S.B., Secondary metabolites responses of plants exposed to ozone: an update. Environmental Science and Pollution Research, 2023, 1–32.
Tak, Y., Kumar, M., Phenolics: a key defence secondary metabolite to counter biotic stress. Plant Phenolics in Sustainable Agriculture 1 (2020), 309–329.
van der Heijden, M.G.A., Martin, F.M., Selosse, M.A., Sanders, I.R., Mycorrhizal ecology and evolution: the past, the present, and the future. New Phytologist 205 (2015), 1406–1423, 10.1111/nph.13288.
Vashishth, D.S., Bachheti, A., Bachheti, R.K., Husen, A., Allelopathic effect of Callistemon viminalis's leaves extract on weeds, soil features, and growth performance of wheat and chickpea plants. Journal of Plant Interactions, 18(1), 2023, 2248172.
Wang, Y., Zhang, W., Zhang, Z., Wang, W., Xu, S., He, X., Isolation, identification and characterization of phenolic acid-degrading bacteria from soil. J. Appl. Microbiol. 131:1 (2021), 208–220.
Wang, J., Yuan, B., Huang, B., Differential heat-induced changes in phenolic acids associated with genotypic variations in heat tolerance for hard fescue. Crop. Sci. 59:2 (2019), 667–674.
Wilhelm, R.C., DeRito, C.M., Shapleigh, J.P., Madsen, E.L., Buckley, D.H., Phenolic acid-degrading Paraburkholderia prime decomposition in forest soil. ISMe Commun., 1, 2021, 4, 10.1038/s43705-021-00009-z.
Xia, Z., He, Y., Korpelainen, H., Niinemets, Ü., Li, C., Sex-specific interactions shape root phenolics and rhizosphere microbial communities in Populus cathayana. For. Ecol. Manage, 504, 2022, 119857.
Xiao, Z., Zou, T., Lu, S., Xu, Z., Soil microorganisms interacting with residue-derived allelochemicals effects on seed germination. Saudi. J. Biol. Sci. 27 (2020), 1057–1065, 10.1016/j.sjbs.2020.01.013.
Xie, J., Tang, W., Zhao, L., Liu, S., Liu, K., Liu, W., Enantioselectivity and allelopathy both have effects on the inhibition of napropamide on Echinochloa crus-galli. Science of the Total Environment 682 (2019), 151–159.
Xu, X., Geng, F., Sun, W., Quantitative proteomics and metabolomics analysis reveals the response mechanism of alfalfa (Medicago sativa L.) to o-coumaric acid stress. PLoS. One, 18, 2023, e0295592.
Yan, Q., Tong, J., Li, S., Peng, Q., Barnyard Grass Stress Triggers Changes in Root Traits and Phytohormone Levels in Allelopathic and Non-Allelopathic Rice. Biology. (Basel), 12(8), 2023, 1074.
Yan, W., McClung, A.M., ‘Rondo’, a long-grain indica rice with resistances to multiple diseases. J. Plant Regist. 4:2 (2010), 131–136.
Yang, P, Azher Nawaz, M, Li, F, Bai, L, Li, J, Brassinosteroids regulate antioxidant system and protect chloroplast ultrastructure of autotoxicity-stressed cucumber (Cucumis sativus L.) seedlings. Agron, 9(5), 2019, 265.
Zhou, P., Li, Q., Liu, G., Xu, N., Yang, Y., Zeng, W., Wang, S., Integrated analysis of transcriptomic and metabolomic data reveals critical metabolic pathways involved in polyphenol biosynthesis in Nicotiana tabacum under chilling stress. Functional plant biology 46:1 (2018), 30–43.
Zhou, X., Wu, F., p-Coumaric acid influenced cucumber rhizosphere soil microbial communities and the growth of Fusarium oxysporum f. sp. cucumerinum Owen. PLoS. One, 7(10), 2012, e48288.
Zhou, X., Wu, F., Vanillic acid changed cucumber (Cucumis sativus L.) seedling rhizosphere total bacterial, Pseudomonas and Bacillus spp. communities. Scientific Reports, 8, 2018, 4929, 10.1038/s41598-018-23406-2.
Ziolkowska, A., Debska, B., Banach-Szott, M., Transformations of phenolic compounds in meadow soils. Sci. Rep., 10, 2020, 19330, 10.1038/s41598-020-76316-7.