ALLELOPATHIC EFFECTS OF CELOSIA ARGENTEA L. ON SPERMOSPHERE MICROORGANISMS

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Int. J. LifeSc. Bt & Pharm. Res. 2013 P Saritha and A Sreeramulu, 2013 Research Paper ISSN 2250-3137 www.ijlbpr.com Vol. 2, No. 1, January 2013 2013 IJLBPR. All Rights Reserved ALLELOPATHIC EFFECTS OF CELOSIA ARGENTEA L. ON SPERMOSPHERE MICROORGANISMS P Saritha 1* and A Sreeramulu 2 *Corresponding Author: P Saritha, sarithapendlikatla@gmail.com Aqueous extracts of root, stem, leaves and flowers of Celosia argentea L promoted the growth of spermosphere microorganisms under laboratory conditions. Shoot leachates were actively promotes the growth of spermosphere microorganisms such as Aspergillus niger, Bacillus subtilis, Fusarium solani and Penicillium notatum. It leads to the production of acids from the microbes into the soil. Hence it is clear that the dormant Celosia argentea L seeds will germinate rapidly under acidic conditions. Whereas roots were inhibitory to the growth of Penicillium and Bacillus species. Keywords: Spermosphere, Allelopathic effects, Celosia argentea L., Aspergillus niger, Bacillus subtilis, Fusarium solani, Penicillium notatum INTRODUCTION Spermosphere microorganisms are effected by allelopathic chemicals exudated by weeds and other plants. Rice (1971) and Rice and Pancholi (1972) have observed the inhibitory effect of weeds on nitrogen fixing plants. Effect of Parthenium hysterophorus extracts on Rhizobium and Azatobacter under laboratory conditions was reported by Sarma (1985) and Sarma et al. (1988). Allelopathic effects of Digera muricata on Azatobacter was reported by Sarma et al. (1999). Assessment of allelopathy among microbes and plants was studied by Elliot and Cheng (1987). Lovett (1987) studied allelopathic effects through bacterial mediation. Lynch (1987) reported the allelopathy involving microorganisms. These studies were initiated to explore the allelopathic effects of C. argentea L. on spermosphere microorganisms. MATERIALS AND METHODS Sterilized conical flasks were taken and 20 ml of PDA medium was distributed into all the conical flasks. Then these conical flasks were divided into four sets.100 mg, 250 mg and 500 mg of root, stem, leaf and flower extracts were weighed. In the first set of conical flasks 100 mg, 250 mg and 500 mg of root extracts were mixed with PDA 1 Department of Botany, S V University, Tirupati, AP 517502. 2 Department of Botany, S V University, Tirupati, AP 517502. 76

Int. J. LifeSc. Bt & Pharm. Res. 2013 P Saritha and A Sreeramulu, 2013 medium separately. Likewise into the 2 nd, 3 rd and 4 th set of conical flasks different quantities of stem, leaf and flower extracts were added respectively. One conical flask containing PDA medium was taken as a control in all the four sets. All the four sets of conical flasks were sterilized by keeping in a autoclave at a pressure of 15 lbs for 30 min. Sterilized petriplates were used. The sterilized media contained 100 mg, 250 mg, and 500 mg of root stem, leaf and flower extracts which were present in the different conical flasks were poured into petriplates separately. In every set one petriplate was taken as a control. Different fungal species viz., Aspergillus niger, Fusarium solani, Penicillium notatum, and Bacillus subtilis were isolated from the sphermosphere of Celosia argentea were spot inoculated into the root, stem, leaf and flower extracts containing PDA media. Then all the petri plates were incubated for 4 to 5 days. The diameter of each colony of grown microorganism was measured and readings were recorded. Results were statistically analyzed. RESULTS Allelopathic Effects of C. argentea Stem Extract The growth of Penicillium notatum and Bacillus subtilis was increases as the concentration of C. argentea stem extract increases (Table 1). But the growth of Aspergillus niger and Fusarium solani was increased up to 250 ppm of stem extract. Allelopathic Effects of C. argentea Flower Extract The growth of Bacillus subtilis and Aspergillus niger was increases as the concentration of C. argentea flower extract increases but, Table 1: The Effect of Stem Extract of C.argentea on Various Microorganisms S.No Name of the Microorganism Concentration of Stem Extract (PPM) Control (cm) 100 (cm) 250 (cm) 500 (cm) 1 Aspergillus niger 0.5 1.0 1.2 1.0 2 Bacillus subtilis 0.7 0.8 0.9 1.0 3 Fusarium solani 1.0 3.5 4.0 3.2 4 Penicillium notatum 0.6 0.8 1.0 1.1 Note: * Anova analysis: p<0.000511. Table 2: The Effect of Stem Extract of C.argentea on Spermosphere Microorganisms S.No Name of the Microorganism Concentration of Stem Extract (PPM) Control (cm) 100 (cm) 250 (cm) 500 (cm) 1 Aspergillus niger 0.6 0.8 0.9 1.0 2 Bacillus subtilis 0.4 0.6 0.7 0.9 3 Fusarium solani 1.0 1.5 2.0 1.0 4 Penicillium notatum 0.3 0.5 0.7 0.6 Note: * p<0.05 (significant at 5% level). 77

Int. J. LifeSc. Bt & Pharm. Res. 2013 P Saritha and A Sreeramulu, 2013 Penicillium notatum and Fusarium solani growth rates increased up to 250 ppm (Table 2). Allelopathic Effect of C. argentea Root Extract The growth rate of Fusarium solani was increases as the concentration of root extract increases but Aspergillus niger growth was inhibited with 500 ppm concentration. Whereas root extract inhibited the growth of Penicillium notatum and Bacillus subtilis (Table 3). DISCUSSION The inhibition of nodulation in Arachis hypogaea and Vigna radiata by the allelopathic effect of Table 3: The Effect of Root Extract of C.argentea on Spermosphere Microorganisms S.No Name of the Microorganism Concentration of Root Extract (PPM) Control (cm) 100 (cm) 250 (cm) 500 (cm) 1 Aspergillus niger 0.4 0.6 0.6 0.5 2 Bacillus subtilis 0.4 0.3 0.3 0.3 3 Fusarium solani 0.3 0.4 0.4 0.5 4 Penicillium notatum 0.2 0.1 0.1 0.1 Note: Anova analysis: * p<0.000511 (Significant at 5% level). Figure 1: The Effect of Celosia argentea L. Plant Extracts on Spermosphere Microorganisms Leaf extract of Celosia argentea L. Flower extract of Celosia argentea L. Stem extract of Celosia argentea L. Root extract of Celosia argentea L. 78

Int. J. LifeSc. Bt & Pharm. Res. 2013 P Saritha and A Sreeramulu, 2013 Digera muricata was reported by Vijayasri et al., (1996). Hence it was thought desirable to study the allelopathic effects of phytoextracts on the growth of microorganisms. In the present study, it is observed that the growth rate of microorganisms increased as the concentration of C. argentea L. shoot leachates increased. But root extracts of C. argentea inhibits the growth of certain microorganisms under laboratory conditions. Hence, it may be assumed that the continuous association of C. argentea which is a weed in the crop fields may reduce the yield by promoting growth of microorganisms. Seed germinability of Celosia argentea L. and its relationship with spermosphere microorganisms was studied by Saritha (2008). Henceforth it clear that the dormant seeds of Celosia argentea L. could germinate in acidic conditions of the soil medium released by soil microorganisms in natural soils. CONCLUSION By following the above results, present study concludes allelopathic effects of C. argentea L. has succeeded in suppressing the yields of cereal crops by promoting the growth of microorganisms. So it is recommended that the weed C. argentea L should be physically removed from crop plant fields before the allelochemicals wash down with the rains. REFERENCES 1. Elliot L F and Cheng H H (1987), Assessment of Allelopathy Among Microbes and Plants, A C S Symp.Ser. Am. Chem. Soc., Vol. 330, pp. 504-515, The Society, Washington DC. 2. Lovett J V (1987), Allelopathy in Australia, Bacterial Mediation, A C S Symposium, Ser, Am. Chem.Soc.,Vol. 330, pp. 147-155, The Society, Washington,DC. 3. Lynch J M (1983), Soil Biotechnology, Microbial Factors in Crop Productivity, p. 191, Blackwell Scientific Publications. 4. Rice E L (1971), Inhibition of Nodulation of Inoculated Legumes by Leaf Leachates from Pioneer Plant Species from Abandonet Fields, Amer. J. Bot., Vol. 58, No. 4, pp. 368-371. 5. Rice E L and Pancholy S K (1972), Inhibition of Nitrification by Climax Ecosystems, Amer. J. Bot., Vol. 59, pp. 1033-1040. 6. Saritha P (2008), Seed Germinability of C. argentea L. and Its Relationship with Spermosphere Microorganisms, Special issue of, Research Journal of Biotechnology, p. 9. 7. Sarma K K V (1985), Effect of Parthenium hysterophorus Extract on Rhizobium, Trop. Ecol., Vol. 26, pp. 85-86. 8. Sarma K K V, Uma M and Vijayasri M (1988), Allelopathic Effects of Parthenium hysterophorus on Rhizobium, Trop. Ecol., Vol. 26, pp. 85-86. 9. Vijayasri M, Prasadu P and Sarma K K V (1996), Allelopathic Potential of Digera muricata (L.) Mart. On Nodulation and Dry Matter Production of Arachis hypogaea L. and Vigna radiata (L.), Wilczac. J. Swamy Bot. Cl., Vol. 13, pp. 39-40. 79