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Pakistan Journal of Biological Sciences

Year: 2020 | Volume: 23 | Issue: 10 | Page No.: 1260-1266
DOI: 10.3923/pjbs.2020.1260.1266
Allelopathic Effect of Calotropis procera, Hyoscyamus muticus and Pulicaria undulata Extracts on Seed Germination of Portulaca oleracea and Chenopodium murale
Nadi Awad Al-Harbi

Abstract: Background and Objective: The use of herbicides leads to severe damage, especially to the environment. The aim of this investigation was operated to study the allelopathic effect of Calotropis procera, Hyoscyamus muticus and Pulicaria undulata aqueous extracts on the seed germination of Portulaca oleracea and Chenopodium murale. Materials and Methods: The aerial parts of the plants (Calotropis procera, Hyoscyamus muticus and Pulicaria undulata) washed well in distilled water and were dried in room temperature then ground to fine powder. Aqueous extract was prepared using distilled water. Results: In this study, different concentrations of plant extracts (1, 3 and 5%) were used to illustrate which of these concentrations have the potential to inhibit seed growth of Portulaca oleracea and Chenopodium murale. Concentration of 5% for all plant extracts used to inhibited the growth of all seeds of Chenopodium murale while, concentration of 5% for Pulicaria undulata extract only inhibited the growth of all seeds of Portulaca oleracea. Conclusion: This work dealt with the use of allelopathy strategy in preventing the growth of some weeds to be one of the safest alternative ways of using herbicides. The results showed the effective effect of plant extracts for both Calotropis procera, Hyoscyamus muticus and Pulicaria undulata on the seed germination of Portulaca oleracea and Chenopodium murale.

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Nadi Awad Al-Harbi , 2020. Allelopathic Effect of Calotropis procera, Hyoscyamus muticus and Pulicaria undulata Extracts on Seed Germination of Portulaca oleracea and Chenopodium murale. Pakistan Journal of Biological Sciences, 23: 1260-1266.

Keywords: Allelopathic, weed control, Calotropis procera, Hyoscyamus muticus, Pulicaria undulata, Portulaca oleracea and Chenopodium murale

INTRODUCTION

Weeds are a component of agroecosystems, but the presence of weeds leads to a huge loss of agricultural crops1-8 up to 36%. The presence of weeds has a strong relationship with the type of crops, as well as soil properties9.

Many methods can be used to control weed growth, such as; chemical, mechanical and biological methods. However, the expansion of herbicides use has been prevalent in the past decades (about 3 million t of herbicides/year was used in agro ecosystems)10,11. Many herbicides can be used to eliminate weeds and increase crop productivity12-15, but the continuous use of herbicides has many harmful effects on the environment, human health concerns, water resources contaminated, soil inefficiency, developing weed resistance and increase natural enemies16-21.

Also, most herbicides are very expensive22. So, it was very important to use beneficial and safer materials on the environment and not expensive such as natural herbicides23-25.

Rice26, Gatti et al.27 and Fritz et al.28 defined allelopathy as “any indirect or direct harmful effect of specific plant on the growth of microorganism or another nearby plant through production of allelopathic materials into the environment”. Allelopathy plays essential role in crop protection, weed control and crop re-establishment. Many weeds have allopathic efficacy on the growing of other weeds29-33. Allelopathic materials are found in many plant parts (roots, stems, leaves, fruits and flowers) as secondary metabolites such as; phenolic acids, flavonoids, alkaloids, terpenoids, isoprenoids, cyanogenic, glycosides, tannins, saponins, cyanohydrins, polyacetylenes, benzoic, unsaturated lactones and coumarins34-40.

Many plant extracts showed allelopathic effects on the growth of many weeds41-43. The most successful allelopathic materials prevent the germination of the most weeds and at the same time do not affect the germination of crops44-62.

The flora of Saudi Arabia includes many native plants which have allelopathic effects on the growth of several weeds45,46,63,64. Several authors have studied the allelopathic effect of Calotropis procera, Hyoscyamus muticus and Pulicaria undulata on different plants47-53.

The present study aimed to assess the allelopathic effect of Calotropis procera, Hyoscyamus muticus and Pulicaria undulata aqueous extracts on the seed germination of Portulaca oleracea and Chenopodium murale.

MATERIALS AND METHODS

Plants and seeds collection: The studied allelopathic plants and the seeds of Portulaca oleracea and Chenopodium murale were collected from Tayma city and surrounding it at the flowering period during Spring of 2018. All plant species were identified according to Migahid54 and Collenette55.

Preparation of extracts: The aerial parts of the plants (Calotropis procera, Hyoscyamus muticus and Pulicaria undulata) washed well in distilled water and were dried in room temperature then ground to fine powder. Aqueous extract was prepared by soaking 100 g air-dried plant powder in 1 L of distilled water at 20-25°C for 1 day with shaker. The mixture was filtered by using filter paper then kept at 5°C until used. From aqueous extracts different concentrations 0, 1, 3 and 5% were prepared, in addition to control (distilled water). The laboratory experiment was done in Petri dish. The experiment was left for 18 days to allow germination of all seeds and finally germination percentage of all seeds, radicle length and plumule length were calculated for each extract. The laboratory experiments were conducted at the laboratory of Biology Department, University College of Tayma, Tabuk University, KSA .

Statistical analysis: Data were statistically analyzed with the aid of CoStat 6.31156 software of analysis of variance57. The means were compared using Duncan at p<0.05.

RESULTS

Radicle and plumule length: The radicle and plumule length of Portulaca oleracea and Chenopodium murale were affected by extracts of Calotropis procera, Hyoscyamus muticus and Pulicaria undulata in most test concentrations (Table 1). There is an inverse relationship between increased concentrations of Calotropis procera and Hyoscyamus muticus extracts and the radicle and plumule length of Portulaca oleracea and Chenopodium murale (Fig. 1, 2). Concentration of 5% for all plant extracts inhibited the growth of all radicles and plumule of Chenopodium murale. While, only concentration of 5% for Pulicaria undulata extract inhibited the growth of plumule and radicle of Portulaca oleracea. The results showed that Pulicaria undulata extract for all concentration has more extracts to prevent the growth of both radicle and plumule of Chenopodium murale (Fig. 3).

Table 1:
Different extracts effect on the radicle and plumule length of Portulaca oleracea and Chenopodium murale
Percentage followed by different letters in the column are significantly different (high) while similar letters indicates small significance according to Duncan's multiple range test at p = 0.05

Fig. 1:
Different extracts effect of Calotropis procera on the radicle and plumule length of Portulaca oleracea and Chenopodium murale

Fig. 2:
Different extracts effect of Hyoscyamus muticus on the radicle and plumule length of Portulaca oleracea and Chenopodium murale

Fig. 3:Different extracts effect of Pulicaria undulata on the radicle and plumule length of Portulaca oleracea and Chenopodium murale

Table 2:
Different extracts effect on the seed germination (%) of Portulaca oleracea and
Percentage followed by different letters in the column are significantly different (high) while similar letters indicates small significance according to Duncan's multiple range test at p = 0.05

Fig. 4:
Different extracts effect of Calotropis procera, Hyoscyamus muticus and Pulicaria undulata on the seed germination (%) of Chenopodium murale

Fig. 5:
Different extracts effect of Calotropis procera, Hyoscyamus muticus and Pulicaria undulata on the seed germination (%) of Portulaca oleracea

Seed germination (%): The seed germination (%) of Portulaca oleracea and Chenopodium murale were affected by extracts of Calotropis procera, Hyoscyamus muticus and Pulicaria undulata in all test concentrations (Table 2). The results showed an inverse relationship between the concentration of extracts and seed germination (%). It should be noted that, Chenopodium murale seed germination (%) was more affected by all concentrations of extracts (Fig. 4). On the other hand, Portulaca oleracea seed germination (%) was less affected by all extracts concentrations (Fig. 5). Concentration of 5% for all plant extracts used to inhibited the growth of all seeds of Chenopodium murale while, concentration of 5% for Pulicaria undulata extract only inhibited the growth of all seeds of Portulaca oleracea.

DISCUSSION

Chenopodium murale is worldwide distributed, but it was usually found in saline and xerophytic habitats58. While, Portulaca oleracea is endemic species in the Mediterranean region and worldwide distributed. In addition to, there are Chenopodium murale and Portulaca oleracea found as a weeds associated with several crops59,60. The presence of weeds in agroecosystems leads to many problems, including reduce crop productivity61. The use of herbicides causes many problems so many other strategies for weed control have been proposed. The use of allelopathic plants was safer for the environment.

In this work, the effect of using different concentrations of aqueous extract form three plants (Calotropis procera, Hyoscyamus muticus and Pulicaria undulata) on the seed germination of Portulaca oleracea and Chenopodium murale was studied. The results showed that, an inverse relationship between increased concentrations of most plant extracts on the seed germination of Portulaca oleracea and Chenopodium murale.

Several previous studies have shown the allelopathic effect of Calotropis procera, Hyoscyamus muticus and Pulicaria undulata on the seed germination of many plants. Aslam et al.52 reported the effect of Calotropis procera on plant growth of wheat and mustard. Al-Zahrani and Al-Robai48 pointed to allelopathic effect of Calotropis procera leaves extract on seed germination of Hordeum vulgare, Senna occidentalis, Triticum aestivum, Trigonella foenum graecum and Cucumis satirus. Nenaah and Ahmed49 indicated that antimicrobial activity of extracts of Calotropis procera. Lázaro et al.50 showed the effect of Calotropis procera aqueous extract on the reproductive efficiency of bovine tick. Al-Humaid and El-Mergawi41 pointed to extract of Pulicaria undulata had allelopathic significant effect on the seed germination of Portulaca oleracea. El-Gawad51 referred to the effect of Pulicaria undulata extract on the germination of Brassica tournefortii. El-Gawad and El-Shora53 reported allelopathic potential of Hyoscyamus muticus on antioxidant system and nucleic acids of Portulaca oleracea. Furthermore, there is an effect of Hyoscyamus muticus extract on the growth of some fungi as Botrytis fabae47. The use of herbicides to limit the growth of weeds leads to many problems such as; affecting human and animal health and soil contamination. So, it can be used extracts of many plants that have the ability to prevent weed growth as a safe alternative to herbicides.

CONCLUSION

This work dealt with the use of allelopathy strategy in preventing the growth of some weeds to be one of the safest alternative ways of using herbicides. The results showed the effective effect of plant extracts for both Calotropis procera, Hyoscyamus muticus and Pulicaria undulata on the seed germination (%) of Portulaca oleracea and Chenopodium murale.

SIGNIFICANCE STATEMENT

This study focused on the importance of plant extracts as allelopathic effect on unwanted weeds. Aqueous extracts of Calotropis procera, Hyoscyamus muticus and Pulicaria undulata on the seed germination of Portulaca oleracea and Chenopodium murale. This paper recommended using natural extracts instead of other chemical uses to rid of unwanted weeds associated with important crops.

REFERENCES

  • Altieri, A.M. and M. Liebman, 1988. Weed Management in Agroecosystem: Ecological Approaches. CRC Press, Florida, pp: 1-6
    Direct Link    


  • Oerke, E.C., H.W. Dehnf, F. Schonbeck and A. Weber, 1994. Crop Production and Crop Protection: Estimated losses in Major Food and Cash Crops. 3rd Edn., Elsevier, Amsterdam, The Netherlands, ISBN-13: 9780444820952, Pages: 808
    Direct Link    


  • Anaya, A.L., 1999. Allelopathy as a tool in the management of biotic resources in agroecosystems. Crit. Rev. Plant Sci., 18: 697-739.
    CrossRef    Direct Link    


  • Singh, V.B. and G. Giri, 2001. Influence of intercropping and weed-control measures on suppression of weeds and productivity of spring season sunflower (Helianthus annuus) and groundnut (Arachis hypogaea). Indian J. Agron., 46: 440-444.


  • Zhang, Z.P., 2001. Weed management in rice in China. Proceedings of the Summary Presented at FAO Workshop on Echinochloa spp. Control, Volume 27, May 27, 2001, Beijing, China, pp: 137-145.


  • Lehoczky, E. and P. Reisinger, 2003. Study on the weed-crop competition for nutrients in maize. Commun. Agric. Applied Biol. Sci., 68: 373-380.
    PubMed    Direct Link    


  • Ahmed, S.A., K.G. El-Rokiek, R.R. El-Masry and N.K. Messiha, 2014. The efficiency of allelochemicals in the seed powder of Eruca sativa in controlling weeds in Pisum sativum. Middle East. J. Agric. Res., 3: 757-762.
    Direct Link    


  • El-Rokiek, K.G., R.R. El-Masry, N.K. Messiha and S.A. Ahmed, 2010. The allelopathic effect of mango leaves on the growth and propagative capacity of purple nutsedge (Cyperus rotundus L.). J. Am. Sci., 6: 151-159.
    Direct Link    


  • Hegazy, A.K., G.M. Fahmy, M.I. Ali and N.H. Gomaa, 2004. Vegetation diversity in natural and agro-ecosystems of arid lands. Community Ecol., 5: 163-176.
    CrossRef    Direct Link    


  • Stephenson, G.R., 2000. Herbicide use and world food production: Risk and Benefits. Proceedings of the Abstract of 3rd International Weed Science Congress, June 6-11, 2000, Foz Do Iguassu, Brazil, pp: 240-.


  • Batish, D.R., K. Arora, H.P. Singh and R.K. Kohli, 2007. Potential utilization of dried powder of Tagetes minuta as a natural herbicide for managing rice weeds. Crop Prot., 26: 566-571.
    CrossRef    Direct Link    


  • Metwally, G.M., 2002. Influence of herbicidal weed control treatments on weed growth, nutrient uptake, yield and yield components of faba bean (Vicia faba L.). J. Agric. Sci. Mansoura Univ., 27: 2185-2196.


  • Abdelhamid, M.T. and I.M. El-Metwally, 2008. Growth, nodulation and yield of soybean and associated weeds as affected by weed management. Planta Daninha, 26: 855-863.
    CrossRef    Direct Link    


  • Soltani, N., R.E. Nurse, D.E. Robinson and P.H. Sikkema, 2008. Response of pinto and small red Mexican bean to postemergence herbicides. Weed Technol., 22: 195-199.
    CrossRef    Direct Link    


  • El-Rokiek, K.G., M.T. Abdelhamid and S.S. El-Din, 2013. Physiological response of purslane weed (Portulaca oleracea) and two common beans (Phaseolus vulgaris) recombinant inbred lines to Phosphorus fertilizer and bentazon herbicide. J. Applied Sci. Res., 9: 2743-2749.


  • Marambe, B. and U.R. Sangakkara, 1996. Non-chemical weed control strategies in low-input farming systems. Commonw. Agric. Digest, 5: 39-67.


  • Duke, S.O., F.E. Dayan, J.G. Romagni and A.N. Rimando, 2000. Natural products as sources of herbicides: Current status and future trends. Weed Res., 40: 99-111.
    CrossRef    Direct Link    


  • Khanh, T.D., M.I. Chung, T.D. Xuan and S. Tawata, 2005. The exploitation of crop allelopathy in sustainable agricultural production. J. Agron. Crop Sci., 191: 172-184.
    CrossRef    Direct Link    


  • Laosinwattana, C., T. Poonpaiboonpipat, M. Teerarak, W. Phuwiwat, T. Mongkolaussavaratana and P. Charoenying, 2009. Allelopathic potential of Chinese rice flower (Aglaia odorata Lour.) as organic herbicide. Allelopathy J., 24: 45-53.
    Direct Link    


  • Bhadoria, P.B.S., 2011. Allelopathy: A natural way towards weed management. Am. J. Exp. Agric., 1: 7-20.
    Direct Link    


  • Poonpaiboonpipat, T., U. Pangnakorn, U. Suvunnamek, M. Teerarak, P. Charoenying and C. Laosinwattana, 2013. Phytotoxic effects of essential oil from Cymbopogon citrates and its physiological mechanisms on barnyardgrass (Echinochloa crus-galli). Ind. Crops Prod., 41: 403-407.
    CrossRef    Direct Link    


  • Kordali, S., A. Cakir, T.A. Akcin, E. Mete, A. Akcin, T. Aydin and H. Kilic, 2009. Antifungal and herbicidal properties of essential oils and n-hexane extracts of Achillea gypsicola Hub-Mor. and Achillea biebersteinii Afan. (Asteraceae). Ind. Crops Prod., 29: 562-570.
    CrossRef    Direct Link    


  • Mahmood, A. and Z.A. Cheema, 2004. Influence of sorghum mulch on purple nutsedge (Cyperus rotundus L.). Int. J. Agric. Biol., 6: 86-88.


  • Masum, S.M., M.A. Hossain, H. Akamine, J.I. Sakagami and P.C. Bhowmik, 2016. Allelopathic potential of indigenous Bangladeshi rice varieties. Weed Biol. Manage., 16: 119-131.
    CrossRef    Direct Link    


  • Trezzi, M.M., R.A. Vidal, A.A. Balbinot Junior, H. von Hertwig Bittencourt and A.P. da Silva Souza Filho, 2016. Allelopathy: Driving mechanisms governing its activity in agriculture. J. Plant Interact., 11: 53-60.
    CrossRef    Direct Link    


  • Rice, E.L., 1984. Allelopathy. 2nd Edn., Academic Press, San Diego, pp: 422
    Direct Link    


  • Gatti, A.B., S.C.J.G. de Andrade Perez and M.I.S. Lima, 2004. Allelopathic activity of aqueous extracts of Aristolochia esperanzae O. Kuntze in the germination and growth of Lactuca sativa L. and Raphanus sativus L. Acta Bot. Bras., 18: 459-492.
    CrossRef    Direct Link    


  • Fritz, D., A.P. Bernardi, J.S. Hass, B.M. Ascoli, S.A.L. Bordignon and G. Poser, 2007. Germination and growth inhibitory effects of Hypericum myrianthum and H. polyanthemum extracts on Lactuca sativa L. Rev. Bras. Farmacogn., 17: 44-48.
    CrossRef    Direct Link    


  • Weston, L.A. and S.O. Duke, 2003. Weed and crop allelopathy. Crit. Rev. Plant Sci., 22: 367-389.
    CrossRef    Direct Link    


  • El-Rokiek, K.G. and R.A. Eid, 2009. Allelopathic effects of Eucalyptus citriodora on Amaryllis and associated grassy weed. Planta Daninha, 27: 887-899.
    CrossRef    Direct Link    


  • Jabran, K., M. Farooq, M. Hussain, H. Rehman and M. Ali, 2010. Wild oat (Avena fatua L.) and canary grass (Phalaris minor Ritz.) management through allelopathy. J. Plant Prot. Res., 50: 41-44.
    CrossRef    Direct Link    


  • Li, Z.H., Q. Wang, X. Ruan, C.D. Pan and D.A. Jiang, 2010. Phenolics and plant allelopathy. Molecules, 15: 8933-8952.
    CrossRef    PubMed    Direct Link    


  • El-Rokiek, K.G., N.K. Messiha, R. R. El-Masry and S.A.S. El-Din, 2011. Evaluating the leaf residues of Eucalyptus globules and Mangifera indica on growth of Cynodon dactylon and Echinochloa colonum. J. Applied Sci. Res., 7: 1793-1799.
    Direct Link    


  • Rice, E.L., 1995. Biological Control of Weeds and Plant Diseases: Advances in Applied Allelopathy. 1st Edn. University Oklahoma Press, Normam, USA., Pages: 488
    Direct Link    


  • Weston, L.A., 1996. Utilization of allelopathy for weed management in agroecosystems. Agron. J., 88: 860-866.
    CrossRef    Direct Link    


  • Singh, H.P., D.R. Batish, S. Kaur and R.K. Kohli, 2003. Phytotoxic interference of Ageratum conyzoides with wheat (Triticum aestivum). J. Agron. Crop Sci., 189: 341-346.
    CrossRef    Direct Link    


  • Noguichi, H.K. and T. Ino, 2001. Assessment of allelopathic potential of root exudate of rice seedlings. Biol. Planta., 44: 635-638.
    CrossRef    Direct Link    


  • Einhellig, F.A., 2004. Mode of Allelochemical Action of Phenolic Compounds. In: Allelopathy: Chemistry and Mode of Action of Allelochemicals, Macias, F.A., J.C.G. Galindo, J.M.G. Molinillo and H.G. Cutler (Eds.). CRC Press, Boca Raton, FL., USA., ISBN-13: 9780849319648, pp: 217-238
    Direct Link    


  • Sanchez-Moreiras, A.M., O.A. Weiss and M.J. Reigosa-Roger, 2004. Allelopathic evidence in the Poaceae. Bot. Rev., 69: 300-319.
    CrossRef    Direct Link    


  • Mahmood, A., Z.A. Cheema, A. Khaliq and A.U. Hassan, 2010. Evaluating the potential of allelopathic plant water extracts in suppressing horse purslane growth. Int. J. Agric. Biol., 12: 581-585.
    Direct Link    


  • Al-Humaid, A. and R.A. El-Mergawi, 2014. Herbicidal activities of seven native plants on the germination and growth of Phalaris minor, Echinochloa crusgalli, Portulaca oleracea and Lactuca sativa. J. Agric. Sci. Technol. A, 4: 843-852.


  • Rawat, L.S., R.K. Maikhuri, Y.M. Bahuguna, N.K. Jha and P.C. Phondani, 2017. Sunflower allelopathy for weed control in agriculture systems. J. Crop Sci. Biotechnol., 20: 45-60.
    CrossRef    Direct Link    


  • Shah, R.H., M.S. Baloch, A.A. Khan, M. Ijaz and M. Zubair, 2018. Bioherbicidal assessment of aqueous extracts of mesquite (Prosopis juliflora) on weeds control and growth, yield and quality of wheat. Planta Daninha, Vol. 36.
    CrossRef    


  • Azirak, S. and S. Karaman, 2008. Allelopathic effect of some essential oils and components on germination of weed species. Acta Agric. Scand. Sect. B-Soil Plant Sci., 58: 88-92.
    CrossRef    Direct Link    


  • Al-Humaid, A.I. and M.O.A. Warrag, 1999. Effect of mesquite (Prosopis juliflora) pericarps aqueous extracts on seed germination and plumule and radicle elongation of bermudagrass (Cynodon dactylon). J. King Saud Univ. Agric. Sci., 11: 149-156.
    Direct Link    


  • El-Mergawi, R. and A. Al-Humaid, 2017. Evaluation the allelopathic potential of fractions obtained from some native plants on Portulaca oleracea and Echinochloa crusgalli weed. Bull. NRC., 41: 273-285.


  • Mahmoud, Y.A.G., M.K.H. Ebrahim and M.M. Aly, 2004. Influence of plant extracts and microbioagents on physiological traits of faba bean infected with Botrytis fabae. J. Plant Biol., 47: 194-202.
    CrossRef    Direct Link    


  • Al-Zahrani, H.S. and S.A. Al-Robai, 2007. Allelopathic effect of Calotropis procera leaves extract on seed germination of some plants. J. King Abdulaziz Univ. Sci., 19: 115-126.
    Direct Link    


  • Nenaah, E.G. and M.E. Ahmed, 2011. Antimicrobial activity of extracts and latex of Calotropis procera (Ait.) and synergistic effect with reference antimicrobials. Res. J. Med. Plant, 5: 706-716.
    CrossRef    Direct Link    


  • Lázaro, S.F., L.D. Fonseca, R.C. Fernandes, J.S. Tolentino, E.R. Martins and E.R. Duarte, 2012. Efeito do extrato aquoso do algodão de seda (Calotropis procera Aiton) sobre a eficiência reprodutiva do carrapato bovino. Rev. Bras. Plantas Med., 14: 302-305.
    CrossRef    Direct Link    


  • Abd El-Gawad, A.M., 2014. Ecology and allelopathic control of Brassica tournefortii in reclaimed areas of the Nile delta, Egypt. Turk. J. Bot., 38: 347-357.
    CrossRef    Direct Link    


  • Aslam, M.M., M. Jamil, I. Malook, A. Khatoon and A. Rehman et al., 2016. Phytotoxic effects of Calotropis procera, Tamarix aphylla and Peganum harmalaon plant growth of wheat and mustard. Pak. J. Agric. Res., 29: 43-51.
    Direct Link    


  • Abd El-Gawad, A.M. and H.M. El-Shora, 2017. Assessment of allelopathic potential of Hyoscyamus muticus L. on antioxidant system and nucleic acids of purslane. Fresen. Environ. Bull., 26: 2147-2155.


  • Migahid, A.M., 1996. Flora of Saudi Arabia. Vol. 1-3, King Abdul Aziz University Press, Jeddah, Saudi Arabia


  • Collenette, S., 1999. Wild Flowers of Saudi Arabia. 1st Edn. National Commission for Wildlife Conservation and Development (NCWCD), Riyadh, Pages: 799
    Direct Link    


  • Gomez, K.A. and A.A. Gomez, 1984. Statistical Procedures for Agricultural Research. 2nd Edn., John Wiley and Sons, New York, USA., ISBN-13: 9780471870920, Pages: 680
    Direct Link    


  • Duncan, D.B., 1955. Multiple range and multiple F tests. Biometrics, 11: 1-42.
    CrossRef    Direct Link    


  • Perveen, A. and M. Qasier, 2012. Pollen flora of Pakistan-LXX: Chenopodiaceae. Pak. J. Bot., 44: 1325-1333.
    Direct Link    


  • Travlos, I.S., P.J. Kanatas, G. Economou, V.E. Kotoulas, D. Chachalis and S. Tsioros, 2012. Evaluation of velvetleaf interference with maize hybrids as influenced by relative time of emergence. Exp. Agric., 48: 127-137.
    CrossRef    Direct Link    


  • Abd El-Ghani, M., A. Soliman, R. Hamdy and E. Bennoba, 2013. Weed flora in the reclaimed lands along the northern sector of the Nile Valley in Egypt. Turk. J. Bot., 37: 464-488.
    Direct Link    


  • Al Harbi, N.A., 2016. Allelopathic potential of Artemisia herba-alba and Anthemis arvensis to control weeds in wheat (Triticum aestivum) and Barley (Hordeum vulgare). South Asian J. Exp. Biol., 6: 95-100.
    Direct Link    


  • Al-Harbi, N.A., 2018. Allelopathic effect of leaf extract of two wild plants on seed germination, shoot and root length of two weed species; Portulaca oleracea and Chenopodium murale. Biosci. Biotechnol. Res. Asia, 15: 929-935.
    CrossRef    Direct Link    


  • Osman, A.K.E. and M.A.E.H. Abdein, 2019. Floristic diversity of Wadi Ar'ar, Saudi Arabia. J. Taibah Univ. Sci., 13: 772-789.
    CrossRef    Direct Link    


  • Alhaithloul, H.A., 2019. Environmental and genetic diversity of rangeland plant species in Saudi Arabia. World J. Environ. Biosci., 8: 57-66.
    Direct Link    

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