Effect of nutrient management practices on soil enzyme activity in finger millet
Abstract
A field experiment was conducted during Kharif, 2022 on sandy loams oils at Indian Institute of oilseed research, Hyderabad to study the effect of nutrient management practices in finger millet. The results revealed that at panicle initiation and harvest stages of finger millet, the activity of urease, dehydrogenase and phosphatase was found highest with application of NPK + 0.2% B + FYM @ 2t ha-1 (N applied in 3 splits (T8)) and this was on par with STB (NPK) + FYM @ 2t ha-1 (N applied in 3 splits (T6)), NPK + 0.2% B (N applied in 2 splits (T7)), STB (NPK) (N applied in 2 splits (T5)) and RDF (N applied in 3 splits (T4)) and lowest was found in control.
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Introduction
Finger millet (Eleusine coracana L. Gaertn) commonly called as Ragi, is an important millet crop grown in India. It is the third most important millet after sorghum and pearl millet with a cultivated area of 1.014 million hectares and production of 1.52 million tonnes, having a productivity of 1747 kg ha -1 . In Telangana, area under Finger millet crop is 1012 hectares, with production of 1200 tonnes and productivity of 1220 kg ha -1 (www.indiastat.com., 2020-2021) [9] . It can be recommended as a contingent crop due to its short duration and ability to withstand harsh weather conditions. Being a C4 crop, it has higher water use efficiency and low input requirements. As this crop shows adapting ability to various ecological conditions, it can be integrated to different cropping systems. Indiscriminate use of fertilizers and continuous application of chemical fertilizers pertaining to N and P only has resulted in stagnant yields due to declined response to blanket fertilizer application. Hence, balanced nutrient management is key in achieving higher yield and to maintain soil fertility. Further, high cost of chemical fertilizers and their negative impacts on soil health have led to growing interest in the organic nutrient management and conjunctive use of organic and chemical sources of nutrients. The enzymes in soil originate from animal, plant and microbial sources and are very much influenced by the addition of organic manures. Soil enzymes are biologically significant as they participate in the nutrient transformation, cycling of mineral elements and influence their availability to plant. Soil enzyme activities are 'sensors or indicators' of soil degradation since they exhibit information about microbial status and physicochemical conditions of soil in relation to nutrients availability. Keeping these points in view the present study was conducted to know the changes of enzyme activities in response to different nutrient management practices in finger millet.
Materials and Methods
A Field experiment was carried during Kharif, 2022 at Indian Institute of Oilseed Research, Hyderabad. The experiment was laid out in randomized complete block design with 9 treatments, replicated thrice. The treatments included were T1: Control, T2: Farmers practice, T3: RDF ( N applied in 2 splits), T4: RDF (N applied in 3 splits), T5: Soil Test Based (NPK) (N applied in 2 splits), T6: Soil Test Based (NPK) + FYM (farm yard manure) @ 2t ha -1 (N applied in 3 splits), T7: NPK + 0.2% B foliar spray at flowering (N applied in 2 splits), T8: NPK + 0.2% B foliar spray at flowering + FYM @ 2t ha -1 (N applied in 3 splits), T 9: FYM + GM (Goat manure) + Azospirillum + PSB (Phosphate solubilizing bacteria) + KSB (Potassium solubilizing bacteria) + ZnSB (Zinc solubilizing bacteria). The recommended dose of fertilizers for finger millet was 50-40-20 kg N, P 2 O 5 and K 2 O ha - 1 . Nitrogen was applied in 2 splits i.e half @ sowing and remaining half @ 30 DAS, when applied in 3 splits 1/3 was applied @ sowing, 1/3 @ 30 DAS remaining as foliar N during panicle initiation stage of finger millet at 45 DAS. Soil Test based recommended dose of fertilizers (65-40-20 N, P 2 O 5 , K 2 O kg ha -1 were applied to treatments T 5 , T 6 and in T 7 and T 8 , limiting micronutrient (Boron), respectively based on initial soil test values. Liquid Biofertilizers (Azospirillum, PSB, KSB and ZnSB each @ 1.25 L ha -1 ) was applied to soil in T 9 treatment. Soil samples were collected at panicle initiation and harvest stages from each treatment in between the plants and were analysed for activity of urease, dehydrogenase, Acid phosphatase and Alkaline phosphatase by following the procedures as described by Bremner and Douglas (1971), [2] Casida et al. (1964) [3] , Evazi and Batabai (1979) [5] and Tabatabai and Bremner (1972) [16] , respectively.
Results and Discussion
The data pertaining to the activities of urease, dehydrogenase, acid and alkaline phosphatases enzymes in soil due to nutrient management practices in finger millet at panicle initiation and harvest stage are presented in Table 1, 2, 3 and4.
Urease activity
The urease activity in soil at panicle initiation stage varied from 18.60 to 34.40 µg NH4+-N g -1 2hr -1 and at harvest stage it was ranged between 14.20 to 30.80 µg NH4+-N g -1 2hr -1 . At both the stages, significantly highest urease activity in soil was recorded in treatment T 8 (34.40 and 30.80 µg NH4+-N g -1 2hr -1 , respectively) which had received recommend dose of NPK + 0.2% B + FYM @ 2t ha -1 , but the total N requirement of the crop was applied in 3 splits i.e., at sowing, 30 DAS and at 45-50 DAS. The effect of this treatment was on noticed to be at par with treatments T 6 , T 7 , T 5 and T 4 (Table1). At panicle initiation and harvest stage significantly lower urease activity was recorded in organics alone (22.30 and 18.20 µg NH4+-N g -1 2hr - 1 , respectively) and control (18.60 and 14.20 µg NH4+-N g -1 2hr - 1 , respectively). Highest urease activity was found in treatments receiving both inorganic source and organic source (T 8 , T 6 , T 4 ). This may be attributed to sufficient supply of energy source i.e. carbon from the organics and readily available nutrients from inorganic fertilizers for the growth of microbes responsible for releasing urease enzyme. Further, application of organic matter provides proper aeration, moisture content and nutrients which resulted in better proliferation of microorganisms. Singaram and Kamala Kumari (2000) [15] reported the enhanced levels of soil enzyme activity due to addition of FYM and Inorganic source. The higher organic matter levels in the farmyard manure treatments might have provided a more favourable environment for the accumulation of enzymes in soil matrix, since soil organic constituents were thought to be important in forming stables complexes with free enzymes (Ramalakshmi et al., 2011 and Vandana et al., 2012) [12,17] . Similarly it was also reported by Yadav et al. (2013) [18] and Reddy et al. (2016) [14] . The urease enzyme activity at harvest was lower than at panicle initiation stage which could be due to lower moisture in soil affecting microbial activity. Levels of soil enzyme activity due to addition of FYM. The higher organic matter levels in the farmyard manure treatments might have provided a more favourable environment for the accumulation of enzymes in soil matrix, since soil organic constituents were thought to be important in forming stables complexes with free enzymes (Ramalakshmi et al., 2011 and Vandana et al., 2012) [12,16] . These results were in consonance with Yadav et al. (2013) [17] and Reddy et al. (2016) [13] . The enzymes activity at harvest was lower than at PI stage which could be due to lower moisture in soil affecting microbial activity.
Dehydrogenase activity
Dehydrogenase activity (DHA) indicates the overall microbial activity in the soil and the data pertaining to it at two growth stages of finger millet is presented in Table 2. At panicle initiation stage, it ranged from 32.41 to 54.21 µg TPF formed g -1 soil day -1 , while at harvest stage it ranged from 25.26 to 42.76 µg TPF formed g -1 soil day -1 . The highest dehydrogenase activity at panicle initiation (54.21 µg TPF formed g -1 soil day -1) and harvest stage (42.76 µg TPF formed g -1 soil day -1 ) was observed in the treatment receiving balanced nutrition in treatment T 8 . The lowest values for both the stages was observed in control (32.41 and 25.26 µg TPF formed g -1 soil day -1 , respectively). Balanced application of nutrients included combined use of organics and inorganics based on actual soil test values in T 8 which recorded 44.13, 44.65 per cent increase over application of organic sources alone (T 9 ) at both the stages, respectively. This might be due to the addition of organic sources which might have created environment conducive for formation of soluble organic carbon pools which might have helped in stimulating the activity of soil microorganisms resulting in an increased DHA in the soil. These results were coincided with the findings of Prasad et al. (2010) [11] and Lee et al. (2004) [7] also reported that soil treated with organic manure showed higher level of dehydrogenase activity as compared to mineral fertilizers applied soil. Build-up of dehydrogenase activity in organics and inorganics treated plots may be due to increased organic carbon content and other nutrient sources that have contributed to the increased soil microorganisms which increased the dehydrogenase activity. These results were coincided with the findings of Mali et al. (2015) [8] and Mounika et al. (2021) [10] .
Acid Phosphatase activity
Soil phosphatase activity are the most important in plant nutrition, these are involved in mineralization of organically bound phosphorus to inorganic phosphorus compounds in soil. The acid phosphatase (AcP) in the soil was significantly affected by nutrient management practices at both the stages of finger millet (Table 3). The highest acid phosphatase activity 27.3, 23.6 μg PNP g -1 soil h -1 at panicle initiation and harvest, respectively) was observed in the treatment (T 8 ) which received balanced nutrition i.e NPK + 0.2% B + FYM @ 2t ha -1 (N applied in 3 splits) and this was on par with T 6 , T 7 and T 4 and lowest was recorded in control (15.6 and 12.50). Higher acid phosphatase activity might be ascribed to the increased population of microorganisms due to availability of substrate. Futher, the organic acids produced during the decomposition of FYM might have resulted in enhanced enzyme activity. These findings are in agreement with the studies of Ramakrishnaiah and Vijaya (2013) [13] .
Alkaline phosphatase activity
The activity of alkaline phosphatase (AlP) followed the same trend of acid phosphatase activity. Significantly highest alkaline phosphatase over control were obtained in balanced nutrition where maximum 38.29, 24.21 μg PNP g -1 soil h -1 was shown by (T 8 ) NPK + 0.2% B + FYM @ 2t ha -1 (N applied in 3 splits) at both the stages of finger millet crop, respectively and it was on par with (T 6 ) Soil Test Based (NPK) + FYM @ 2t ha -1 (N applied in 3 splits), (T7) NPK + 0.2% B foliar spray at flowering (N applied in 2 splits), (T 5 ) Soil Test Based (NPK) (N was applied in 2 splits) and (T 4 ) RDF (N was applied 3 splits). Higher alkaline activity in soil might be due to the reason that microbes continuously produce and secrete the enzyme necessary for degradation of their substrate (food). Roots might have secreted organic acids and carbohydrates, which stimulate higher soil enzyme activities. In all the treatments the acid and alkaline phosphatase activity exhibited highest activity at panicle initiation and thereafter the activity gradually decreased at harvest. The sharp increase in the enzyme activities at panicle initiation stage which coincides with the active growth stage of the crop, enhanced root activity and the release of extracellular enzymes like urease and phosphatase into soil solutions during the active growth phase which resulted in higher rate of mineralization of nutrients in the soil. The results were in conformity with the findings of Jagadeesh (2000) [6] , Datt et al., (2013) [4] and Aher et al., (2015) [1] . Further, the treatments receiving only organics (T 9 ) showed decrease in phosphatase activity might be due to non-availability of phosphorous source for microbial growth which might have affected the enzyme activity as the P in organic sources gets released slowly.
Conclusion
From the foregoing discussion, it is clear that in all the treatments soil enzymes (urease, dehydrogenase and phosphatases) exhibited more activity at panicle initiation, there after activity was reduced at harvest of finger millet crop. Balanced application of nutrients based on actual soil test values utilising both organic and inorganic sources (NPK + 0.2% B + FYM @ 2t ha -1 ) registered significantly highest urease, dehydrogenase and phosphatase activity at panicle initiation and harvest stages of finger millet crop, which in turn can enhance nutrient availability to plants through faster mineralization processes.
References
- Aher SB, Lakaria BL, Kaleshananda S, Singh AB, Ramana S, Ramesh K, et al. Effect of organic farming practices on soil and performance of soybean (Glycine max) under semiarid tropical conditions in Central India. Journal of Applied and Natural Science. 2015;7(1): 67-71.
- Bremner JM, Douglas LA. Inhibition of urease activity in soils. Soil Biology and Biochemistry. 1971;9:105-108.
- Casida L, Klein D, Santoro T. Soil dehydrogenase activity. Soil Science. 1964;98:371-376.
- Datt N, Dubey YP, Chaudhary R. Studies on impact of organic, inorganic and integrated use of nutrients on symbiotic parameters, yield, and quality of French-bean (Phaseolus vulgaris L). African Journal of Agricultural Research. 2013;8 (22):2645-2654.
- Evazi F, Tabatabai MA. Phosphatase in soil. Soil Biology and Biochemistry. 1977;9:167-172.
- Jagadeesh BR. Chemical and biochemical properties of soil subjected to permanent manurial and cropping schedule. Journal of the Indian Society Soil Science. 2000;48(2):283286.
- Lee CH, Park CY, Park KD, Jeon WT, Kim PJ. Long-term effects of fertilization on the forms and availability of soil phosphorus in paddy. Chemosphere. 2004;56(3):299-304.
- Mali DV, Kharche VK, Jadhao SD, Jadhao SM, Saoji BV, Gite PA. Soil biological health under long-term fertilization in sorghum-wheat sequence on swell-shrink International Journal of Research in Agronomy. Journal of the Indian Society of Soil Science. 2015;63(4):423-428.
- Mounika K, Kumari AL, Sujani Rao CH, Luther M. Soil biological properties influenced by organics and biofertilizers in rabi sorghum. The Pharma Innovation Journal. 2021;10(7):80-84.
- Prasad J, Karamkar S, Kumar R, Mishra B. Influence of integrated nutrient management on yield and soil properties in maize -wheat cropping system in an Alfisol of Jharkhand. Journal of the Indian Society of Soil Science. 2010;58(2):200-204.
- Ramalakshmi CS, Rao PC, Sreelatha T, Padmaja G, Madhavi M, Rao PV, et al. Effect of nutrient management (INM) on humic substances and micro nutrient status in submerged rice soils. Journal of Rice Research. 2011;6(1):57 -65.
- Ramakrishnaiah G, Vijaya T. Influence of VAM fungi, Azotobacter sp. and PSB on soil phosphatase activity and nutrients (N, P, K, Cu, Zn, Fe and Mn) status in the rhizosphere of Stevia rebaudiana (Bert.) plants. American Journal of Plant Sciences. 2013;4:1443-1447.
- Reddy KPC, Murthy IYLN, Mahadevappa SG, Reddy NS. Effect of integrated use of inorganic and organic sources of nutrients on available nutrient status, inorganic P fractions, and enzyme activity in soil after harvest of maize in maize - groundnut cropping sequence in Alfisols. Progressive Research -An International Journal. 2016;11(4):3708-3712.
- Singaram P, Kamalakumari K. Long-term effect of FYM and fertilizers on enzyme dynamics of soil. Journal of the Indian Society Soil Science. 2005;43(3):378-381.
- Tabatabai MA, Bremner JM. Use of p-nitrophenyl phosphate for assay of soil phosphatase activity. Soil Biology and Biochemistry. 1969;1:301-307
- Vandana LJ, Rao PC, Padmaja G. Effect of crop cover on soil enzyme activity. The Journal of Research, ANGRAU. 2012;40(4):1-5.
- Yadav SK, Babu S, Singh Y, Yadav MK, Yadav GS, Pal S, et al. Effect of organic nutrient sources on yield, nutrient uptake, and soil biological properties of rice -based cropping sequence. Indian Journal of Agronomy. 2013;58(3):70-75.
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