Comparison of the efficiency of efficient and mountain microorganisms in composting organic waste
DOI:
https://doi.org/10.70099/BJ/2025.02.01.7Keywords:
compost, organic waste, organic matter, decomposition, odor intensityAbstract
The purpose of this research was to evaluate the decomposition process of organic waste from juice factories in a local market, using mountain microorganisms (MM) and efficient microorganisms (EM) to determine the macronutrients and physical and chemical properties of the product (compost). The methodology used was to simultaneously decompose a certain amount of organic waste with ME and MM independently to verify the process's speed and intensity of odor. It was constantly evaluated three times a week, progressively allowing data collection and observation. The results indicate that the organic matter of the compost increased by 364.29% with the work of the MM and an increase of 296.43% ME; the sand of the compost experienced a 14.15% increase with MM and a 10.52% increase with ME. The apparent density of the compost experiences a 2.09% increase with the incorporation of mountain and efficient microorganisms. Compost nitrogen increased by 467.46% with the addition of MM and 472.62% with ME. Organic waste decomposes 98% after seven weeks with MM and 100% with efficient microorganisms.
References
1. SINIA. Estudio de Caracterización de los Residuos Sólidos Domiciliarias de la ciudad de Moyobamba - Julio 2012 | SINIA. 2012. Accessed August 7, 2024. https://sinia.minam.gob.pe/documentos/estudio-caracterizacion-residuos-solidos-domiciliarias-ciudad
2. Ma J, Zhang L, Mu L, Zhu K, Li A. Multivariate insights of bulking agents influence on co-biodrying of sewage sludge and food waste: Process performance, organics degradation and microbial community. Sci Total Environ. 2019;681:18-27. doi:10.1016/j.scitotenv.2019.05.101
3. Zhang Y, Liang Z, Tang C, et al. Malodorous gases production from food wastes decomposition by indigenous microorganisms. Sci Total Environ. 2020;717:137175. doi:10.1016/j.scitotenv.2020.137175
4. Aldonate ML, Jiménez P, Ulla EL. Caracterización de rizobacterias nativas y su efecto en la promoción de crecimiento de garbanzo (Cicer arietinum L.) en condiciones controladas. Rev Agronómica Noroeste Argent. 2019;39(2):89-98.
5. Saha S, Jeon BH, Kurade MB, et al. Interspecies microbial nexus facilitated methanation of polysaccharidic wastes. Bioresour Technol. 2019;289:121638. doi:10.1016/j.biortech.2019.121638
6. Liang C, Das KC, McClendon RW. The influence of temperature and moisture contents regimes on the aerobic microbial activity of a biosolids composting blend. Bioresour Technol. 2003;86(2):131-137. doi:10.1016/s0960-8524(02)00153-0
7. Tanya Morocho M, Leiva-Mora M, Tanya Morocho M, Leiva-Mora M. Microorganismos eficientes, propiedades funcionales y aplicaciones agrícolas. Cent Agríc. 2019;46(2):93-103.
8. Joshi H, Somdutt, Choudhary P, Mundra SL. Role of Effective Microorganisms (EM) in Sustainable Agriculture. Int J Curr Microbiol Appl Sci. 2019;8(3):172-181. doi:10.20546/ijcmas.2019.803.024
9. Zhu L, Zhao Y, Zhang W, et al. Roles of bacterial community in the transformation of organic nitrogen toward enhanced bioavailability during composting with different wastes. Bioresour Technol. 2019;285:121326. doi:10.1016/j.biortech.2019.121326
10. Qin R, Su C, Mo T, et al. Effect of excess sludge and food waste feeding ratio on the nutrient fractions, and bacterial and fungal community during aerobic co-composting. Bioresour Technol. 2021;320:124339. doi:10.1016/j.biortech.2020.124339
11. Avila GM de A, Gabardo G, Clock DC, Junior OS de L. Use of efficient microorganisms in agriculture. Res Soc Dev. 2021;10(8):e40610817515-e40610817515. doi:10.33448/rsd-v10i8.17515
12. Mahmood A, Iguchi R, Kataoka R. Fertilizante multifuncional para residuos alimentarios con capacidad de inhibición del crecimiento de Fusarium y solubilidad en fosfato: un nuevo horizonte para el reciclaje de residuos alimentarios utilizando microorganismos. Waste Manag. 2019;94:77-84. doi:10.1016/j.wasman.2019.05.046
13. Kulwa F, Li C, Zhao X, et al. A State-of-the-Art Survey for Microorganism Image Segmentation Methods and Future Potential. IEEE Access. 2019;7:100243-100269. doi:10.1109/ACCESS.2019.2930111
14. Sekhohola-Dlamini L, Tekere M. Microbiology of municipal solid waste landfills: a review of microbial dynamics and ecological influences in waste bioprocessing. Biodegradation. 2020;31(1-2):1-21. doi:10.1007/s10532-019-09890-x
15. Ferdeș M, Dincă MN, Moiceanu G, Zăbavă B Ștefania, Paraschiv G. Microorganisms and Enzymes Used in the Biological Pretreatment of the Substrate to Enhance Biogas Production: A Review. Sustainability. 2020;12(17):7205. doi:10.3390/su12177205
16. Palaniveloo K, Amran MA, Norhashim NA, et al. Food Waste Composting and Microbial Community Structure Profiling. Processes. 2020;8(6):723. doi:10.3390/pr8060723
17. Pachiega R, Rodrigues MF, Rodrigues CV, et al. Hydrogen bioproduction with anaerobic bacteria consortium from brewery wastewater. Int J Hydrog Energy. 2019;44(1):155-163. doi:10.1016/j.ijhydene.2018.02.107
18. Mengqi Z, Shi A, Ajmal M, Ye L, Awais M. Comprehensive review on agricultural waste utilization and high-temperature fermentation and composting. Biomass Convers Biorefinery. 2023;13(7):5445-5468. doi:10.1007/s13399-021-01438-5
19. Sun C, Wei Y, Kou J, et al. Improve spent mushroom substrate decomposition, bacterial community and mature compost quality by adding cellulase during composting. J Clean Prod. 2021;299:126928. doi:10.1016/j.jclepro.2021.126928
20. Zhu R, Liu C, Xu YD, et al. Ratio of carbon and nitrogen in fertilizer treatment drives distinct rhizosphere microbial community composition and co-occurrence networks. Front Microbiol. 2022;13. doi:10.3389/fmicb.2022.968551
21. Ghinea C, Leahu A. Monitoring of Fruit and Vegetable Waste Composting Process: Relationship between Microorganisms and Physico-Chemical Parameters. Processes. 2020;8(3):302. doi:10.3390/pr8030302
22. Wan L, Wang X, Cong C, et al. Effect of inoculating microorganisms in chicken manure composting with maize straw. Bioresour Technol. 2020;301:122730. doi:10.1016/j.biortech.2019.122730
23. Ayilara MS, Olanrewaju OS, Babalola OO, Odeyemi O. Waste Management through Composting: Challenges and Potentials. Sustainability. 2020;12(11):4456. doi:10.3390/su12114456
24. Liu H, Tan X, Guo J, Liang X, Xie Q, Chen S. Bioremediation of oil-contaminated soil by combination of soil conditioner and microorganism. J Soils Sediments. 2020;20(4):2121-2129. doi:10.1007/s11368-020-02591-6
25. Hamid HA, Qi LP, Harun H, et al. Development of Organic Fertilizer from Food Waste by Composting in UTHM Campus Pagoh. J Appl Chem Nat Resour. 2019;1(1). Accessed August 7, 2024. https://fazpublishing.com/jacnar/index.php/jacnar/article/view/4
26. Chew KW, Chia SR, Yen HW, Nomanbhay S, Ho YC, Show PL. Transformation of Biomass Waste into Sustainable Organic Fertilizers. Sustainability. 2019;11(8):2266. doi:10.3390/su11082266
27. Carlessi S, Meza R. Metodología y Diseños en la Investigación Científica. 5ta ed. [Internet]. [lugar desconocido]: [editor desconocido]; 2015 [citado 31 de julio de 2024]. Disponible en: https://www.academia.edu/78002369/METODOLOG%C3%8DA_Y_DISE%C3%91OS_EN_LA_INVESTIGACI%C3%93N_CIENT%C3%8DFICA
28. Hernández Sampieri R, Fernández Collado C, Baptista Lucio P. Metodología de la investigación. McGraw Hill España; 2014. Accessed August 1, 2024. https://dialnet.unirioja.es/servlet/libro?codigo=775008
29. Fomina M, Skorochod I. Microbial Interaction with Clay Minerals and Its Environmental and Biotechnological Implications. Minerals. 2020;10(10):861. doi:10.3390/min10100861
30. Dlamini P, Sekhohola-Dlamini LM, Cowan AK. Editorial: Soil-microbial interactions. Front Microbiol. 2023;14. doi:10.3389/fmicb.2023.1213834
31. Ontman R, Groffman PM, Driscoll CT, Cheng Z. Surprising relationships between soil pH and microbial biomass and activity in a northern hardwood forest. Biogeochemistry. 2023;163(3):265-277. doi:10.1007/s10533-023-01031-0
32. Lee YH, Ahn BK, Sonn YK. Effects of Electrical Conductivity on the Soil Microbial Community in a Controled Horticultural Land for Strawberry Cultivation. Korean J Soil Sci Fertil. 2011;44(5):830-835. doi:10.7745/KJSSF.2011.44.5.830
33. Karhu K, Alaei S, Li J, Merilä P, Ostonen I, Bengtson P. Microbial carbon use efficiency and priming of soil organic matter mineralization by glucose additions in boreal forest soils with different C:N ratios. Soil Biol Biochem. 2022;167:108615. doi:10.1016/j.soilbio.2022.108615
34. Manral V, Bargali K, Bargali SS, Karki H, Chaturvedi RK. Seasonal Dynamics of Soil Microbial Biomass C, N and P along an Altitudinal Gradient in Central Himalaya, India. Sustainability. 2023;15(2):1651. doi:10.3390/su15021651
35. Mo L, Zanella A, Bolzonella C, et al. Land Use, Microorganisms, and Soil Organic Carbon: Putting the Pieces Together. Diversity. 2022;14(8):638. doi:10.3390/d14080638
36. Ouyang N, Zhang P, Zhang Y, et al. Cation Exchange Properties of Subsurface Soil in Mid-Subtropical China: Variations, Correlation with Soil-Forming Factors, and Prediction. Agronomy. 2023;13(3):741. doi:10.3390/agronomy13030741
37. Chávez Barrientos N. Efecto de microorganismos eficientes en la disponibilidad de fósforo y rendimiento del cacao a 560 msnm - Kimbiri - Cusco. Published online 2018. Accessed August 7, 2024. http://repositorio.unsch.edu.pe/handle/UNSCH/3267
38. Mazahar S, Umar S. Soil Potassium Availability and Role of Microorganisms in Influencing Potassium Availability to Plants. In: Iqbal N, Umar S, eds. Role of Potassium in Abiotic Stress. Springer Nature; 2022:77-87. doi:10.1007/978-981-16-4461-0_4
39. Sarikhani MR, Oustan S, Ebrahimi M, Aliasgharzad N. Isolation and identification of potassium-releasing bacteria in soil and assessment of their ability to release potassium for plants. Eur J Soil Sci. 2018;69(6):1078-1086. doi:10.1111/ejss.12708
40. Neumann D, Heuer A, Hemkemeyer M, Martens R, Tebbe CC. Response of microbial communities to long-term fertilization depends on their microhabitat. FEMS Microbiol Ecol. 2013;86(1):71-84. doi:10.1111/1574-6941.12092
41. Zakavi M, Askari H, Shahrooei M. Characterization of bacterial diversity between two coastal regions with heterogeneous soil texture. Sci Rep. 2022;12(1):18901. doi:10.1038/s41598-022-23487-0
42. Kapinusova G, Lopez Marin MA, Uhlik O. Reaching unreachables: Obstacles and successes of microbial cultivation and their reasons. Front Microbiol. 2023;14. doi:10.3389/fmicb.2023.1089630
43. Seaton FM, George PBL, Lebron I, Jones DL, Creer S, Robinson DA. Soil textural heterogeneity impacts bacterial but not fungal diversity. Soil Biol Biochem. 2020;144:107766. doi:10.1016/j.soilbio.2020.107766
44. Dorodnikov M, Blagodatskaya E, Blagodatsky S, Fangmeier A, Kuzyakov Y. Stimulation of r - vs. K -selected microorganisms by elevated atmospheric CO 2 depends on soil aggregate size. FEMS Microbiol Ecol. 2009;69(1):43-52. doi:10.1111/j.1574-6941.2009.00697.x
45. Harris K, Young IM, Gilligan CA, Otten W, Ritz K. Effect of bulk density on the spatial organisation of the fungus Rhizoctonia solani in soil. FEMS Microbiol Ecol. 2003;44(1):45-56. doi:10.1111/j.1574-6941.2003.tb01089.x
46. Abdelkhalik A, Abd El-Mageed TA, Mohamed IAA, et al. Soil application of effective microorganisms and nitrogen alleviates salt stress in hot pepper (Capsicum annum L.) plants. Front Plant Sci. 2023;13. doi:10.3389/fpls.2022.1079260
47. O'Brien FJM, Almaraz M, Foster MA, et al. Soil Salinity and pH Drive Soil Bacterial Community Composition and Diversity Along a Lateritic Slope in the Avon River Critical Zone Observatory, Western Australia. Front Microbiol. 2019;10. doi:10.3389/fmicb.2019.01486
48. Liang C, Balser TC. Warming and nitrogen deposition lessen microbial residue contribution to soil carbon pool. Nat Commun. 2012;3(1):1222. doi:10.1038/ncomms2224
49. Bahadori M, Wang JT, Shen J pei, Lewis S, Rezaei Rashti M, Chen C. Soil organic matter and geochemical characteristics shape microbial community composition and structure across different land uses in an Australian wet tropical catchment. Land Degrad Dev. 2022;33(6):817-831. doi:10.1002/ldr.4174
50. Qu R, Liu G, Yue M, et al. Soil temperature, microbial biomass and enzyme activity are the critical factors affecting soil respiration in different soil layers in Ziwuling Mountains, China. Front Microbiol. 2023;14. doi:10.3389/fmicb.2023.1105723
51. Kästner M, Miltner A, Thiele-Bruhn S, Liang C. Microbial Necromass in Soils—Linking Microbes to Soil Processes and Carbon Turnover. Front Environ Sci. 2021;9. doi:10.3389/fenvs.2021.756378
52. Grzyb A, Wolna-Maruwka A, Niewiadomska A. The Significance of Microbial Transformation of Nitrogen Compounds in the Light of Integrated Crop Management. Agronomy. 2021;11(7):1415. doi:10.3390/agronomy11071415
53. Farrell M, Prendergast-Miller M, Jones DL, Hill PW, Condron LM. Soil microbial organic nitrogen uptake is regulated by carbon availability. Soil Biol Biochem. 2014;77:261-267. doi:10.1016/j.soilbio.2014.07.003
54. Stark S, Kumar M, Myrsky E, et al. Decreased Soil Microbial Nitrogen Under Vegetation 'Shrubification' in the Subarctic Forest–Tundra Ecotone: The Potential Role of Increasing Nutrient Competition Between Plants and Soil Microorganisms. Ecosystems. 2023;26(7):1504-1523. doi:10.1007/s10021-023-00847-z
55. Silva LI da, Pereira MC, Carvalho AMX de, Buttrós VH, Pasqual M, Dória J. Phosphorus-Solubilizing Microorganisms: A Key to Sustainable Agriculture. Agriculture. 2023;13(2):462. doi:10.3390/agriculture13020462
56. Timofeeva A, Galyamova M, Sedykh S. Prospects for Using Phosphate-Solubilizing Microorganisms as Natural Fertilizers in Agriculture. Plants. 2022;11(16):2119. doi:10.3390/plants11162119
57. Beltran-Medina I, Romero-Perdomo F, Molano-Chavez, Lady, Gutiérrez AY, Silva AMM, Estrada-Bonilla G. Inoculation of phosphate-solubilizing bacteria improves soil phosphorus mobilization and maize productivity. Nutr Cycl Agroecosystems. 2023;126(1):21-34. doi:10.1007/s10705-023-10268-y
58. Zhang C, Kong F. Isolation and identification of potassium-solubilizing bacteria from tobacco rhizospheric soil and their effect on tobacco plants. Appl Soil Ecol. 2014;82:18-25. doi:10.1016/j.apsoil.2014.05.002
59. Olaniyan FT, Alori ET, Adekiya AO, et al. The use of soil microbial potassium solubilizers in potassium nutrient availability in soil and its dynamics. Ann Microbiol. 2022;72(1):45. doi:10.1186/s13213-022-01701-8
60. Pereira DGC, Santana IA, Megda MM, Megda MXV. Potassium chloride: impacts on soil microbial activity and nitrogen mineralization. Ciênc Rural. 2019;49:e20180556. doi:10.1590/0103-8478cr20180556
61. Turpault MP, Bonnaud P, Fighter J, Ranger J, Dambrine E. Distribution of cation exchange capacity between organic matter and mineral fractions in acid forest soils (Vosges mountains, France). Eur J Soil Sci. 1996;47(4):545-556. doi:10.1111/j.1365-2389.1996.tb01854.x
62. Barragán OAD, Robayo DMM, Caballero JAL. Revista Colombia Forestal. Colomb For. 2009;12(1):141-160. doi:10.14483/udistrital.jour.colomb.for.2009.1.a10
63. Chaparro-Acuña SP, Becerra-Jiménez ML, Martínez-Zambrano JJ, Rojas-Sarmiento HA. Soil bacteria that precipitate calcium carbonate: mechanism and applications of the process. Acta Agronómica. 2018;67(2):277-288. doi:10.15446/acag.v67n2.66109
64. Gomez MG, Graddy CMR, DeJong JT, Nelson DC. Biogeochemical Changes During Bio-cementation Mediated by Stimulated and Augmented Ureolytic Microorganisms. Sci Rep. 2019;9(1):11517. doi:10.1038/s41598-019-47973-0
65. Mokrani S, Nabti E hafid, Cruz C. Recent Trends in Microbial Approaches for Soil Desalination. Appl Sci. 2022;12(7):3586. doi:10.3390/app12073586
66. Nguyen MK, Lin C, Hoang HG, et al. Investigation of biochar amendments on odor reduction and their characteristics during food waste co-composting. Sci Total Environ. 2023;865:161128. doi:10.1016/j.scitotenv.2022.161128
67. Margaritis M, Dimos V, Malamis D, Loizidou M. An experimental investigation of the composting process in an innovative home composting System: The influence of additives. Clean Mater. 2023;8:100185. doi:10.1016/j.clema.2023.100185
68. Wu H, Cui H, Fu C, et al. Unveiling the crucial role of soil microorganisms in carbon cycling: A review. Sci Total Environ. 2024;909:168627. doi:10.1016/j.scitotenv.2023.168627
69. Pei Yuan R, Yanbing L, Siqi H. Role of microbes and microbial dynamics during composting. In: ResearchGate. ; 2023. doi:10.1016/B978-0-323-91874-9.00011-5
70. Ahmed T, Noman M, Qi Y, et al. Fertilization of Microbial Composts: A Technology for Improving Stress Resilience in Plants. Plants. 2023;12(20):3550. doi:10.3390/plants12203550
71. (PDF) EFFECTIVE MICROORGANISMS: A REVIEW OF THEIR PRODUCTS AND USES. ResearchGate. Published online October 22, 2024. doi:10.5455/NJEAS.147954
72. Pan I, Dam B, Sen SK. Composting of common organic wastes using microbial inoculants. 3 Biotech. 2012;2(2):127-134. doi:10.1007/s13205-011-0033-5
73. Kodaparthi A de, Venkateswar Reddy K, Kehkashaan L, Venkatesh Belli M. Conservación ambiental para una agricultura sostenible | Solicitar PDF. January 2024. Accessed December 1, 2024. https://www.researchgate.net/publication/378487181_Environmental_Conservation_for_Sustainable_Agriculture
74. Muhammad Muhammad S. (PDF) Unveiling the Roles of Microorganisms in Promoting Environmental Sustainability. ResearchGate. 2024;63-74. doi:10.58578/AJSTEA.v1i1.1783
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