Optimization of Indole-3-Acetic Acid and Cutting Type for Enhanced Vegetative Propagation of Vetiver (Vetiveria zizanioides L.)
DOI:
https://doi.org/10.24925/turjaf.v14i8.2343-2352.8707Keywords:
Auxin, Cutting type, Propagation, Rooting performance, VetiverAbstract
Vegetative propagation is a key method for the rapid multiplication and establishment of vetiver (Chrysopogon zizanioides). However, its success is often limited by poor rooting making the use of plant growth regulators such as indole-3-acetic acid (IAA) essential for improving propagation efficiency. This study evaluated the effects of different concentrations of IAA on the vegetative propagation of three types of vetiver cuttings: semi-hardwood (SHW), semi-softwood (SSW), and tillers. This was aimed at identifying the optimum concentration of IAA for rooting and growth of vetiver as well as determining the best cutting type for effective propagation of the plant, with a view to enhancing its vegetative propagation. The experiment was a 3 × 10 factorial arranged in a completely randomized design with seven replications. Cuttings were treated with 10 different IAA concentrations ranging from 0 to 100 ppm. Parameters assessed included root initiation period, number of newly formed tillers, number of leaves and leaf length, number of roots and root length, and dry weights of leaves and roots. Data generated were analyzed with SPSS 20 and significant means were separated using Fisher’s Least Significant Difference at p<0.05. Results showed that application of IAA reduced significantly (p<0.05) period of root initiation from 35 days in the control to 3-13 days in the IAA-treated cuttings with 25 ppm having the shortest root initiation period. In addition, IAA significantly (p<0.05) enhanced all the growth parameters assessed compared to untreated controls, with 25 ppm consistently yielding the best results. At this concentration and when averaged across all treatments, highest number of newly formed tillers (15), number of leaves (82), leaf length (115.35 cm), number of roots (95), root length (68.30 cm), and dry weights of leaves (1.81 g) and roots (1.77 g) were recorded. Higher IAA concentrations (>35 ppm) generally led to reduced growth and biomass production. Among the various cuttings, the tillers consistently outperformed SHW and SSW across all parameters. These findings show that moderate concentrations of IAA, particularly 25 ppm, significantly improved vegetative propagation efficiency and establishment of vetiver, with tillers being the best cutting type.
References
Abdalla, N., El-Ramady, H., Seliem, M. K., El-Mahrouk, M. E., Taha, N., Bayoumi, Y., Shalaby, T. A., & Dobránszki, J. (2022). An academic and technical overview on plant micropropagation challenges. Horticulturae, 8(8), 677. https://doi.org/10.3390/horticulturae8080677
AOAC (2016). Official Methods of Analysis of AOAC International (20th ed.). Rockville, MD, USA.
Badhon, F. F., Islam, M. S., & Islam, M. A. (2021). Contribution of vetiver root on the improvement of slope stability. Indian Geotechnical Journal, 51, 829–840. https://doi.org/10.1007/s40098-021-00557-0 .
Balasubramanian, V. K., Rivas-Ubach, A., Winkler, T., Mitchell, H., Moran, J., & Ahkami, A. H. (2024). Modulation of polar auxin transport identifies the molecular determinants of source–sink carbon relationships and sink strength in poplar. Tree Physiology, 44(13), 82–101. https://doi.org/10.1093/treephys/tpad073
Banerjee, R., Goswami, P., Lavania, S., Mukherjee, A., & Lavania, U. C. (2019). Vetiver grass is a potential candidate for phytoremediation of iron ore mine spoil dumps. Ecological Engineering, 132, 120–136. https://doi.org/10.1016/j.ecoleng.2018.10.012
Brewer, P. B., Dun, E. A., Ferguson, B. J., Rameau, C., & Beveridge, C. A. (2009). Strigolactone acts downstream of auxin to regulate bud outgrowth in pea and Arabidopsis. Plant Physiology, 162(2), 1040–1050. https://doi.org/10.1104/pp.108.134783.
David, A., Farcas, A., & Socai, S. A. (2023). An overview of the chemical composition and bioactivities of Vetiveria zizanioides (L.) Nash essential oil. Trends in Food Science and Technology, 140. https://doi.org/10.1016/j.tifs.2023.104153
De Klerk, G. J., van der Krieken, W., & de Jong, J. C. (1999). The formation of adventitious roots: New concepts, new possibilities. In Vitro Cellular & Developmental Biology – Plant, 35(3), 189–199. https://doi.org/10.1007/s11627-999-0076-z
Domagalska, M. A., & Leyser, O. (2011). Signal integration in the control of shoot branching. Nature Reviews Molecular Cell Biology, 12(4), 211–221. https://doi.org/10.1038/nrm3088.
El-Sallami, I. H., Gad, M. M., Hussein, M. F., & Ebeid, A. F. (2018). Roles of auxins and propagation time in rooting of Kigelia pinnata Jacq. cuttings. Assiut Journal of Agricultural Sciences, 49(1), 133-147. https://doi.org/10.21608/ajas.2018.8200
Guan, K., Li, Y., Zhang, Y., Yang, J., Ge, Z., & Dai, X. (2025). Transcriptomic and physiological insights into auxin-mediated root growth and potassium uptake in tobacco under low-potassium stress. BMC Plant Biology 25, 664. https://doi.org/10.1186/s12870-025-06600-z
Guan, L., Tayengwa, R., Cheng, Z., Peer, W.A., Murphy, A.S., & Zhao, M. (2019). Auxin regulates adventitious root formation in tomato cuttings. BMC Plant Biology, 19(1), 435. https://doi.org/10.1186/s12870-019-2002-9
Hartmann, H. T., Kester, D. E., Davies, F. T., & Geneve, R. L. (2011). Plant propagation: principles and practices (8th ed.). Prentice Hall.
Holanda, F. S. R., Santos, L. D. V., Pedrotti, A., Filho, R. N. A., Sartor, L. S., Santos-Sobrinho, V. R. A., de Jesus, R. J. S., Silva, P. A. O., & Andrade, K. M. A. (2022). Evaluation of the root system of Vetiver grass (Chrysopogon zizanioides L. Roberty) using different sampling methods. Environmental System Research, 11, Article 16. https://doi.org/10.1186/s40068-022-00262-8
Itusha, A., Osborne, W. J., & Vaithilingam, M. (2019). Enhanced uptake of Cd by biofilm forming Cd resistant plant growth promoting bacteria bioaugmented to the rhizosphere of Vetiveria zizanioides. International Journal of Phytoremediation, 21, 487–495. https://doi.org/10.1080/15226514.2018.1537245
Kaushik, S., & Shukla, N. (2020). A review on effect of IBA and NAA and their combination on the rooting of stem cuttings of different ornamental crops. Journal of Pharmacognosy and Phytochemistry, 9(3), 1881-1885.
Kumar, R., Ahmed, N., Sharma, O. C., & Lal, S. (2014). Influence of auxins on rooting efficacy in Carnation (Dianthus caryophyllus L.) cuttings. Journal of Horticultural Sciences, 9(2), 157-160. https://doi.org/10.24154/jhs.v9i2.187
Kunc, P., Medič, A., Hudina, M., Veberič, R., & Osterc, G. (2025). Physiological age of stock plants determines phytohormonal changes in leafy cuttings of Prunus subhirtella ‘Autumnalis’. Journal of Plant Growth Regulation, 44, 721–730. https://doi.org/10.1007/s00344-024-11479-5
Lakehal, A., & Bellini, C. (2019). Control of adventitious root formation: Insights into synergistic and antagonistic hormonal interactions. Physiologia Plantarum, 165(1), 90–100. https://doi.org/10.1111/ppl.12823
Liu, Y., Xu, J., Ding, Y., Wang, Q., Li, G., & Wang, S. (2011). Auxin inhibits the outgrowth of tiller buds in rice (Oryza sativa L.) by downregulating OsIPT expression and cytokinin biosynthesis in nodes. Australian Journal of Crop Science, 5(2), 169-174.
Ludwig-Müller, J., Vertocnik, A., & Town, C. D. (2005). Analysis of indole-3-butyric acid-induced adventitious root formation on Arabidopsis stem segments, Journal of Experimental Botany, 56(418), 2095-2105. https://doi.org/10.1093/jxb/eri208
Mohamed, G. A. (2017). Water soaking duration, Indole butyric acid and rooting media and their effect on rooting ability of Ramsey grapevine rootstock cuttings. Middle East Journal of Applied Sciences, 7(4), 1080-1100.
Oshunsanya, S. O., & Aliku, O. (2017). Vetiver grass: a tool for sustainable agriculture. In Grasses - benefits, diversities and functional Roles (pp. 143-148). INTECHOPEN. https://doi.org/10.5772/intechopen.69303
Overvoorde, P., Fukaki, H., & Beeckman, T. (2010). Auxin control of root development. Cold Spring Harbor Perspectives in Biology, 2(6), a001537. https://doi.org/10.1101/cshperspect.a001537
Qin, H., He, L., & Huang, R. (2019). The coordination of ethylene and other hormones in primary root development. Frontiers in Plant Science, 10, 874. https://doi.org/10.3389/fpls.2019.00874
Rout, G. R. (2006). Effect of Auxins on adventitious root development from single node cuttings of Camellia sinensis (L.) Kuntze and associated biochemical changes. Plant Growth Regulation, 48(2), 111–117. https://doi.org/10.1007/s10725-005-5665-1
Roy, T., Mandal, T., Chowdhuri, T. K., Maiti, P., Mandal, S., Rahaman, A., Ahmed, M., Roy, B., Venkatesh, C., & Rathour, T. P. (2024). Effect of different growth regulators on the rooting of hardwood cuttings of Bougainvillea glabra var. Mohan. Journal of Advances in Biology & Biotechnology 2 (8), 1197-1202. https://doi.org/10.9734/jabb/2024/v27i81243.
Stuepp, C. A., Wendling, I., Trueman, S. J., Koehler, H. S., & Zuffellato-Ribas, K. C. (2017). The use of auxin quantification for understanding clonal tree propagation. Forests, 8(1), 27. https://doi.org/10.3390/f8010027
Taiz, L., Zeiger, E., Møller, I. M., & Murphy, A. (2015). Plant physiology and development (6th ed.). Sinauer Associates.
Truong, P. N. V. (2002). Vetiver grass technology. In M. Maffei (ed.). Vetiveria: The Genus Vetiveria (pp. 114-132). Taylor & Francis.
Vidoz, M. L., Loreti, E., Mensuali, A., Alpi, A., & Perata, P. (2010). Hormonal interplay during adventitious root formation in flooded tomato plants. The Plant Journal, 63(4), 551–562. https://doi.org/10.1111/j.1365-313X.2010.04262.x
Vielba, J. M., Vidal, N., José, M. C. S., Rico, S., & Sánchez, C. (2020). Recent advances in adventitious root formation in chestnut. Plants, 9, 1543. https://doi.org/10.3390/plants9111543
Wang, S., Sun, G., Luo, Y., Qian, W., Fan, K., Ding, Z., & Hu, J. (2022). Role of IAA and primary metabolites in two rounds of adventitious root formation in softwood cuttings of Camellia sinensis (L.). Agronomy, 12(10), 2486. https://doi.org/10.3390/agronomy12102486
Wei, K., Ruan, L., Wang, L., & Cheng, H. (2019). Auxin-induced adventitious root formation in nodal cuttings of Camellia sinensis. International Journal of Molecular Science, 20(19), 4817. https://doi.org/10.3390/ijms20194817
Zhao, Y. (2010). Auxin biosynthesis and its role in plant development. Annual Review of Plant Biology, 61, 49-64.
Zhao, Y., Chen, Y., Jiang, C., Lu, M. Z., & Zhang, J. (2022). Exogenous hormones supplementation improve adventitious root formation in woody plants. Frontiers in Bioengineering and Biotechnology, 10, 1009531. https://doi.org/10.3389/fbioe.2022.1009531
Zheng, L., Xiao, Z., & Song, W. (2020). Effects of substrate and exogenous auxin on the adventitious rooting of Dianthus caryophyllus L. HortScience, 55(2), 170–173. https://doi.org/10.21273/HORTSCI14334-19
Downloads
Published
How to Cite
Issue
Section
License

This work is licensed under a Creative Commons Attribution-NonCommercial 4.0 International License.
This work is licensed under a Creative Commons Attribution-NonCommercial 4.0 International License.

