Please wait a minute...
Journal of Integrative Agriculture  2016, Vol. 15 Issue (7): 1521-1531    DOI: 10.1016/S2095-3119(15)61256-4
Plant Protection Advanced Online Publication | Current Issue | Archive | Adv Search |
Effects of Tinospora tuberculata leaf methanol extract on seedling growth of rice and associated weed species in hydroponic culture
Farzad Aslani1*, Abdul Shukor Juraimi1*, Muhammad Saiful Ahmad-Hamdani1, Farahnaz Sadat Golestan Hashemi2, Md Amirul Alam3, Md Abdul Hakim2, Md Kamal Uddin4
1 Department of Crop Science, Faculty of Agriculture, Universiti Putra Malaysia (UPM), Serdang 43400, Malaysia
2 Institute of Tropical Agriculture, Universiti Putra Malaysia (UPM), Serdang 43400, Malaysia
3 School of Agriculture Science and Biotechnology, Faculty of Bioresources and Food Industry, Universiti Sultan Zainal Abidin, Tembila Campus, 22200 Besut, Terengganu, Malaysia
4 Department of Land Management, Faculty of Agriculture, Universiti Putra Malaysia (UPM), Serdang 43400, Malaysia
Download:  PDF in ScienceDirect  
Export:  BibTeX | EndNote (RIS)      
Abstract      The study was conducted to evaluate the responses of rice and rice weed seedlings (barnyardgrass and weedy rice) at the three-leaf stage to Tinospora tuberculata leaf methanol extract (3.12, 6.25 and 12.5 g L–1) under hydroponic culture. It shows that the leaf methanol extract had various degrees effects depending on target plant species and each tested index (biomass, root length, shoot length, transpiration volume, chlorophyll a, chlorophyll b and carotenoid contents). The effective concentration of the leaf extract capable of reducing 50% of rice growth was higher than those of target weed species. Moreover, the root length was more tolerant to leaf methanol extract in comparison to the other plant parameters measured. A greater reduction was observed in chlorophyll a content compared to chlorophyll b and carotenoid. The results revealed that the reduction of transpiration volume closely coincided with the magnitude of growth inhibition of tested plants. Ultra-fast liquid chromatography analysis revealed 11 of 32 peaks in chemical profile, including benzoic acid, caffeic acid, chlorogenic acid, isoorientin, isovitexin, orientin, p-anisic acid, syringic acid, trans-cinnamic acid, trans-ferulic acid, and vitexin have the same retention time with those peaks of the extract. The amount of compounds was present in the range of between 4 817 and 115.5 mg kg–1 dry weight (DW). The concentration-response bioassay of all 11 individual compounds and their equimolar mixture against the seeds of barnyardgrass revealed their contribution in the allelopahic activity of T. tuberculata leaf extract. The examined compounds and their combination exhibited various degrees of growth inhibitory effects on the early growth of barnyardgrass. Therefore, the specific number, concentration, combination and inhibitory activity of bioactive compounds leads to allelopathy activity of T. tuberculata leaves which could be employable directly as a natural herbicide and its growth inhibitor compounds can be used as a template for producing new herbicides.
Keywords:  allelochemicals        identification and quantification        natural herbicide        UFLC        weed control  
Received: 21 September 2015   Accepted:
Fund: 

The authors would also like to thank the Long-Term Research Grant Scheme (LRGS), the Food Security Project, Ministry of Higher Education, Malaysia (5525001) and the Fundamental Research Grant Scheme, Malaysia (07-01-13-1241FR) for providing financial supports.

Corresponding Authors:  Farzad Aslani, Tel: +60-12-9134508, E-mail: aslani.farzad.1362@gmail.com    

Cite this article: 

Farzad Aslani, Abdul Shukor Juraimi, Muhammad Saiful Ahmad-Hamdani, Farahnaz Sadat Golestan Hashemi, Md Amirul Alam, Md Abdul Hakim, Md Kamal Uddin. 2016. Effects of Tinospora tuberculata leaf methanol extract on seedling growth of rice and associated weed species in hydroponic culture. Journal of Integrative Agriculture, 15(7): 1521-1531.

Al Harun M A Y, Johnson J, Uddin M N, Robinson R W. 2015. Identification and phytotoxicity assessment of phenolic compounds in Chrysanthemoides monilifera subsp. monilifera (Boneseed). PLoS ONE, 10, e0139992.

Al-Johani N S, Aytah A A, Boutraa T. 2012. Allelopathic impact of two weeds, Chenopodium murale and Malva parviflora on growth and photosynthesis of barley (Hordeum vulgare L.). Pakistan Journal of Botany, 44, 1865–1872.

An M, Pratley J, Haig T. 2001. Phytotoxicity of vulpia residues: III. Biological activity of identified allelochemicals from Vulpia myuros. Journal of Chemical Ecology, 27, 383–394.

Araniti F, Lupini A, Mercati F, Statti G A, Abenavoli M R. 2013. Calamintha nepeta L. (Savi) as source of phytotoxic compounds: Bio-guided fractionation in identifying biological active molecules. Acta Physiologiae Plantarum, 35, 1979–1988.

Araniti F, Marrelli M, Lupini A, Mercati F, Statti G A, Abenavoli M R. 2014a. Phytotoxic activity of Cachrys pungens Jan, a mediterranean species: Separation, identification and quantification of potential allelochemicals. Acta Physiologiae Plantarum, 36, 1071–1083.

Araniti F, Sunseri F, Abenavoli M R. 2014b. Phytotoxic activity and phytochemical characterization of Lotus ornithopodioides L., a spontaneous species of Mediterranean area. Phytochemistry Letters, 8, 179–183.

Aslani F, Juraimi A S, Ahmad-Hamdani M S, Alam M A, Hashemi F S G, Omar D, Hakim M A. 2015. Phytotoxic interference of volatile organic compounds and water extracts of Tinospora tuberculata Beumee on growth of weeds in rice fields. South African Journal of Botany, 100, 132–140.

Aslani F, Juraimi A S, Ahmad-Hamdani M S, Omar D, Alam M A, Hashemi F S G, Hakim M A, Uddin M K. 2014. Allelopathic effect of methanol extracts from Tinospora tuberculata on selected crops and rice weeds. Acta Agriculturae Scandinavica (Section B - Soil & Plant Science), 64, 165–177.

Aslani F, Juraimi A S, Ahmad-Hamdani M S, Omar D, Alam M A, Hakim M A, Uddin M K. 2013. Allelopathic effects of Batawali (Tinospora tuberculata) on germination and seedling growth of plants. Research on Crops, 14, 1222–1231.

Batish D R, Arora K, Singh H P, Kohli R K. 2007a. Potential utilization of dried powder of Tagetes minuta as a natural herbicide for managing rice weeds. Crop Protection, 26, 566–571.

Batish D R, Kaur M, Singh H P, Kohli R K. 2007b. Phytotoxicity of a medicinal plant, Anisomeles indica, against Phalaris minor and its potential use as natural herbicide in wheat fields. Crop Protection, 26, 948–952.

Beltran J C, Pannell D J, Doole G J, White B. 2012. A bioeconomic model for analysis of integrated weed management strategies for annual barnyardgrass (Echinochloa crus-galli complex) in Philippine rice farming systems. Agricultural Systems, 112, 1–10.

Bodenhofer U, Kothmeier A, Hochreiter S. 2011. APCluster: An R package for affinity propagation clustering. Bioinformatics, 27, 2463–2464.

Brethour C, Weersink A. 2001. An economic evaluation of the environmental benefits from pesticide reduction. Agricultural Economics, 25, 219–226.

Chon S, Kim Y, Lee J. 2003. Herbicidal potential and quantification of causative allelochemicals from several compositae weeds. Weed Research, 43, 444–450.

D’Abrosca B, Scognamiglio M, Fiumano V, Esposito A, Choi Y H, Verpoorte R, Fiorentino A. 2013. Plant bioassay to assess the effects of allelochemicals on the metabolome of the target species Aegilops geniculata by an NMR-based approach. Phytochemistry, 93, 27–40.

Elisante F, Tarimo M T, Ndakidemi P A. 2013. Allelopathic effect of seed and leaf aqueous extracts of Datura stramonium on leaf chlorophyll content, shoot and root elongation of Cenchrus ciliaris and Neonotonia wightii. American Journal of Plant Sciences, 4, 2332–2339.

Forman L. 1981. A Revision of Tinospora (Menispermaceae) in Asia to Australia and the Pacific: The Menispermaceae of Malesia and Adjacent Areas: X. Kew Bulletin. Springer on Behalf of Royal Botanic Gardens, Kew.  pp. 375–421.

He H, Wang H, Fang C, Lin Y, Zeng C, Wu L, Guo W, Lin W. 2009. Herbicidal effect of a combination of oxygenic terpenoids on Echinochloa crus-galli. Weed Research, 49, 183–192.

Hoagland D R, Arnon D I. 1950. The water-culture method for growing plants without soil. In: Circular. 2nd ed. California Agricultural Experiment Station, USA. p. 347.

Hong N H, Xuan T D, Eiji T, Khanh T D. 2004. Paddy weed control by higher plants from Southeast Asia. Crop Protection, 23, 255–261.

IRRI (International Rice Research Institute). 2009. Rice ecosystems. [2015-09-01]. http://www.ppippic.org/ppiweb/filelib.nsf/0/6191D544DF714DEF48257074002E78E6/$file/Rice%20HB%20 2–5.pdf

Kato-Noguchi H, Takeshita S, Kimura F, Ohno O, Suenaga K. 2013. A novel substance with allelopathic activity in Ginkgo biloba. Journal of Plant Physiology, 170, 1595–1599.

Khanh T D, Hong N H, Xuan T D, Chung I M. 2005. Paddy weed control by medicinal and leguminous plants from Southeast Asia. Crop Protection, 24, 421–431.

Lichtenthaler H K. 1987. Chlorophyls and carotenoids: Pigments of photosynthetic biomembranes. Methods in Enzymology, 148, 350–382.

Lokajová V, Ba?korová M, Ba?kor M. 2014. Allelopathic effects of lichen secondary metabolites and their naturally occurring mixtures on cultures of aposymbiotically grown lichen photobiont Trebouxia erici (Chlorophyta). South African Journal of Botany, 93, 86–91.

Mahajan G, Chauhan B S. 2013. The role of cultivars in managing weeds in dry-seeded rice production systems. Crop Protection, 49, 52–57.

Marles S M, Warkentin T D, Holm F A. 2010. Field pea seed residue: A potential alternative weed control agent. Weed Science, 58, 433–441.

Omezzine F, Ladhari A, Rinez A, Haouala R. 2011. Potent herbicidal activity of Inula crithmoïdes L. Scientia Horticulturae, 130, 853–861.

Patterson D. 1981. Effects of allelopathic chemicals on growth and physiological responses of soybean (Glycine max). Weed Science, 29, 53–59.

Pukclai P, Kato-Noguchi H. 2012. Allelopathic potential of Tinospora tuberculata Beumee on twelve test plants species. Journal of Plant Biology Research, 1, 19–28.

Rashid M H, Alam M M, Rao A, Ladha J. 2012. Comparative efficacy of pretilachlor and hand weeding in managing weeds and improving the productivity and net income of wet-seeded rice in Bangladesh. Field Crops Research, 128, 17–26.

Saito K. 2010. Weed pressure level and the correlation between weed competitiveness and rice yield without weed competition: An analysis of empirical data. Field Crops Research, 117, 1–8.

Seck P A, Diagne A, Mohanty S, Wopereis M C. 2012. Crops that feed the world 7: Rice. Food Security, 4, 7–24.

Siddique M A B, Ismail B. 2013. Allelopathic effects of Fimbristylis miliacea on the physiological activities of five Malaysian rice varieties. Australian Journal of Crop Science, 7, 2062–2067.

Da Silva E A D, Lobo L T, Da Silva G A, Souza Filho, Antonio Pedro Da S, Da Silva M N, Arruda A C, Guilhon G, Santos L S, Arruda M S. 2013. Flavonoids from leaves of Derris urucu: Assessment of potential effects on seed germination and development of weeds. Annals of the Brazilian Academy of Sciences, 85, 881–889.

Sodaeizadeh H, Rafieiolhossaini M, Havlík J, Van Damme P. 2009. Allelopathic activity of different plant parts of Peganum harmala L. and identification of their growth inhibitors substances. Plant Growth Regulation, 59, 227–236.

Tesio F, Weston L A, Ferrero A. 2011. Allelochemicals identified from Jerusalem artichoke (Helianthus tuberosus L.) residues and their potential inhibitory activity in the field and laboratory. Scientia Horticulturae, 129, 361–368.

Verdeguer M, Blázquez M A, Boira H. 2009. Phytotoxic effects of Lantana camara, Eucalyptus camaldulensis and Eriocephalus africanus essential oils in weeds of Mediterranean summer crops. Biochemical Systematics and Ecology, 37, 362–369.

Weir T L, Park S, Vivanco J M. 2004. Biochemical and physiological mechanisms mediated by allelochemicals. Current Opinion in Plant Biology, 7, 472–479.

Yang C, Chang F, Lin S, Chou C. 2004. Effects of three allelopathic phenolics on chlorophyll accumulation of rice (Oryza sativa) seedlings: II. Stimulation of consumption-orientation. Botanical Bulletin of Academia Sinica, 45, 119–125.

Zeng R S. 2014. Allelopathy - The solution is indirect. Journal of Chemical Ecology, 40, 515–516.

Zhou Y, Yu J. 2006. Allelochemicals and photosynthesis. In: Allelopathy. Springer, The Netherlands. pp. 127–139.
[1] SUN Yuan-yuan, ZHANG Qiu-xin, ZHAO Yun-peng, DIAO Yue-hui, GUI Fu-rong, YANG Guo-qing. Beneficial rhizobacterium provides positive plant–soil feedback effects to Ageratina adenophora[J]. >Journal of Integrative Agriculture, 2021, 20(5): 1327-1335.
[2] LIU Ying, LIANG Ping-zhuo, LI Fen, MA Kang-sheng, CHEN Xue-wei, CHEN An-qi, LIANG Pei, GAO Xi-wu. The impact of allelochemicals on the differential expression of symbiotic bacteria in cotton aphids[J]. >Journal of Integrative Agriculture, 2018, 17(08): 1815-1821.
[3] Wioletta Biel, Slawomir Stankowski, Anna Jaroszewska, Stanislaw Pu?yński, Paulina Bo?ko. The influence of selected agronomic factors on the chemical composition of spelt wheat (Triticum aestivum ssp. spelta L.) grain[J]. >Journal of Integrative Agriculture, 2016, 15(8): 1763-1669.
No Suggested Reading articles found!