Abstract
Currently, sustainable agriculture involves ecofriendly techniques, which include biofertilization. Biofertilizers increase plant productivity by improving soil fertility and nutrient content. A wide range of living organisms can be applied as biofertilizers and increase soil fertility without causing pollution due to their biodegradability. The organisms can be microorganisms like bacteria, microalgae, and micro fungi or macro organisms like macroalgae, macro fungi, and higher plants. Biofertilizers extracted from living organisms or their residues will be increasingly used rather than chemical fertilizers, which cause heavy metal accumulation in soil. Biofertilizer use aims for sustainable development in agriculture by maintaining the soil. This will mitigate climate change and related impacts and will also lower many serious diseases resulting from pollution such as cancer, liver and renal failure, and immune diseases. This review is a comprehensive overview of biofertilizers extracted from a range of living organisms from the Kingdoms Monera to Plantae and included bacteria, algae, fungi, and higher plants. Organisms that play a vital role in elevating soil nutrients in a safe, cheap, and ecofriendly manner are included in the review to promote their potential commercial application.
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Introduction
The world population is projected to increase to over 10 billion people over the next 30 years. Therefore, food supply will need to rise by 60% in order to fulfil the predicted demand in 2050 (Pambuka et al. 2021, 2022; Kinge et al. 2022). Food distribution and manufacturing must be handled in a more effective and sustainable manner to prevent supply shortages. To do this, farmers are using organic fertilizers, which are made from recycled material such as manure, agricultural residues, and town sewage, including human waste (Ju et al. 2005). The misuse of pesticides and inorganic fertilizers contributed to the desertification of agricultural land and diminishing crop productivity and increased serious human disorders (Bedair et al. 2022b). So, it is necessary to explore biofertilization to obtain healthy food (Ammar 2022).
The soil ecosystem has been severely harmed by inorganic fertilizers, herbicides, and insecticides. Future crop growth will be hampered by this type of treatment on the soil. Currently, the use of natural plant bio stimulants is advocated as an inventive approach to meet the difficulties of sustainable agriculture and to assure optimal nutrient uptake, crop output, and resistance to abiotic stress (Povero et al. 2016). In order to promote the growth of high yield crops, fertilizers are necessary. Many crops on most soils require significant amounts of fundamental nutrients that plants need for healthy growth and include nitrogen (NH4+ or NO3), phosphorus (H2PO4), calcium (Ca2+), sulfur (SO42−), magnesium (Mg2+), potassium (K+), iron (Fe2+ or Fe3+), and zinc (Zn2+ or Zn(OH)2) (White and Brown 2010).
Regardless of the amount of nutrients in the crop, bio stimulants are natural compounds or microorganisms that are administered to plants to increase their nutritional efficiency, resistance to abiotic stress, and qualitative attributes (Abdelsalam et al. 2022). As a subclass of bio stimulants, biofertilizers are microbial inoculants that can enhance the nutritional efficiency of plants by containing active or inactive formulations of advantageous microorganisms (Deepak et al. 2015; Backer et al. 2018; Alori and Babalola 2018).
Since synthetic fertilizers are of chemical origin, over application cause eutrophication, harmful to both soil and plants. Synthetic fertilizers find their way into the adjacent streams and rivers, where they contaminate water and harm fish and other aquatic animals (Sabry 2015). Plants, on the other hand, gradually and safely deliver nutrients to the soil. Many of the plants that are used to fertilize soil are initially planted as cover crops to prevent soil erosion from wind and rain. Enhancing soil fertility requires maintaining a healthy topsoil layer (Thornbro 2022), so scientists currently seek to find new technologies to manufacture new ecofriendly fertilizers from living organisms, especially microbes, which have the ability to biodegrade without any residues.
Biofertilizers enhance crop yield by about 10 to 40% and increase proteins, vital amino acids, vitamins, and nitrogen fixation (Bhardwaj et al. 2014; Shahwar et al. 2023). Biofertilizers have been suggested as a replacement for mineral fertilizers. For instance, nitrogen- and/or sulfur-fixing microorganisms have been used in biofertilizers (Demoling et al. 2007; Beneduzi et al. 2008; Singh and Reddy 2012; Heba et al. 2021) and include bacteria like Azotobacter, Azospirillum, and Rhizobium as well as fungi like Aspergillus niger and A. tubingensis. Genetically altered bacterial strains have been created and tested as biological fertilizers (Sharma et al. 2013). As a natural substitute for synthetic fertilizers, bacterial and fungal biofertilizers have gained popularity. However, their current application has been reduced due to their low effectiveness compared to conventional fertilizers (Nehl et al. 1997; Deepak et al. 2015; Alori and Babalola 2018). Many species of soil bacteria and fungi, which live in beneficial associations, act as ecofriendly soil fertilizers (Ammar et al. 2022; Aioub et al. 2022). Cyanobacteria such as Nostoc sp., Anabaena sp., and Oscillatoria angustissima are potential sources of biofertilizers (Ammar et al. 2022). Cover crops contribute to the safe and gradual delivery of nutrients to the soil and stop soil erosion from wind and rain. Maintaining a sound topsoil layer is necessary for increasing soil fertility.
Plants are frequently used in permaculture to increase soil fertility and residues of some plants such as Musa paradisiaca, Coffea arabica, and Lathyrus oleraceus can be used as soil fertilizers (Singh et al. 2013). Biofertilizers are compounds that include microorganisms and, when given to the soil, improve soil fertility and encourage plant development. In order to boost the nutrient content of the soil and thus the production, biofertilization is a sustainable agricultural practice. It has been discovered that soil microflora can increase soil fertility and boost biomass productivity and is acknowledged as an appropriate environmentally acceptable bio-based fertilizer used in agriculture to prevent pollution. Most cyanobacteria can fix nitrogen from the environment. There are three ways in which extracts of living organisms are applied as biofertilizers: foliar application (spray), soil amendment, and seed imbibition (Fig. 1).
This review summarizes the use of all types of eco-friendly biofertilizers and highlights the efficacy of biofertilizers above inorganic fertilizers. Natural biofertilizers offer high eco-economic value, reduce the risk of plant diseases, less harmful to people than inorganic fertilizers, minimize pollution, and improve soil fertility without heavy metal and residue accumulation over time due to their biodegradability (Ammar 2022).
Bacteria as biofertilizers
Bacterial biofertilizers can increase plant growth and development through a series of various mechanisms (Kumar et al. 2022). These include the production of plant nutrients or phytohormones that can be absorbed by plants, the mobilization of soil compounds so that they are readily available for the plant to use as nutrients, and lastly, the protection of plants under stressful conditions. The later mechanisms help in counteracting the negative effects of stressor defense against plant pathogens, reducing plant diseases or death of the plant. Many plant growth-promoting rhizobacteria (PGPR) have been utilized for a long time as biofertilizers all over the world. They help to increase crop yields and soil fertility, which has the potential to help make agriculture and forestry more sustainable. The market for bacterial-based biofertilizers is expanding, and the production and application of bacterial inocula technologies are constantly being developed and improved (Garcia-Gonzalez and Sommerfeld 2016). For instance, Azotobacter has been extensively researched under laboratory and field conditions and has been employed as a biofertilizer for more than a century. Azotobacter fixes nitrogen (endophytically) in the rhizosphere and roots of rice, that promotes the growth and development of rice. The findings demonstrated that Azotobacter fixes atmospheric nitrogen in the rhizosphere and as an endophyte in rice and produces phytohormones and plant growth stimulants. In addition to fixing nitogen, these bacteria break down insoluble phosphate and boost plant growth (Tualar 2013; Dar et al. 2021; Daniel et al. 2022) (Tables 1 and 2).
On the other hand, Cyanobacteria are the oldest and most productive prokaryote group on earth and include a wide range of organisms. Cyanobacteria biomass or extracts greatly enhanced the physical and chemical properties of soil. Cyanobacteria are also widely recognized for producing biologically active compounds that are effective against plant pathogens and in the phytoremediation of industrial wastewater (Bedair et al. 2022a, b). Therefore, as natural biofertilizers, they contribute significantly to nutrient cycling, phosphorus bioavailability, N2-fixation, environmental protection, and disease control, and improve plant growth and production. Radiative energy is also transformed into chemical energy by cyanobacteria. Through photosynthesis, these biological systems produce oxygen. Food, energy, secondary metabolites, cosmetics, and pharmaceuticals are all products of these species. By lowering CO2 levels through environmentally benign large-scale growth of cyanobacteria, several high-value items can be produced. Thus in the long run, Cyanobacteria biofertilizers could take the place of chemical fertilizers (Gören-Sağlam 2021; Mishra et al. 2021; Bhuyan et al. 2022) (Tables 1 and 2). For instance, Anabaena azollae is a heterocystous filamentous cyanobacterium that fixes nitrogen and grows symbiotically in specific leaf cavities of the tiny eukaryotic water fern Azolla pinnata. Anabaena azollae is grown and used in synthetic medium such as BG-110. Azollae is a promising natural bio-source with potential uses in industry, medicine, and agriculture. Indole acetic acid, gibberellic acid, bioactive like fatty acids, polysaccharides, and phenolic compounds were isolated from A. azollae and reported to have microbicidal activities in vitro and in vivo. Additionally, the high nitrogenase activity of A. azollae has long been recognized as a predictor biofertilization capacity. The enhanced dehydrogenase activity and associated polysaccharide excretion increased soil fertility by expanding the microbial populations (Adhikari et al. 2020; Bao et al. 2021; Abd El-Aal 2022) (Fig. 2, Tables 1 and 2).
Similarly, Nitrobacter biofertilizer reduces gas emissions in rice farming, which is one of the main sources of CH4 emissions. It generates between 5 and 19% of the world’s overall CH4 emissions. Using the closed chamber method, the weekly CH4, CO2, and N2O gas fluxes were measured during a rice-growing season. The treatment of straw plus biofertilizers decreased the emissions of CH4, N2O, and CO2 by 9.2, 14.78, and 27.68%, respectively, compared to straw alone. When compared to only applying straw, the application of straw plus biofertilizers reduced global warming potential by 10.75%. The treatment with straw plus biofertilizer reduced the greenhouse gas index by 8.27% as compared to the control. The findings suggested that using biofertilizer could be environmentally friendly and promote local food security (Rani et al. 2021; Yulianingsih et al. 2021) (Tables 1 and 2). For example, Nitrobacter biofertilizer was researched using a two-factor factorial experiment with randomized block design with different varieties of shallots and at varying concentrations. The results demonstrated that Nitrobacter biofertilizer treatment produced favorable outcomes for the quantity of bulbs per cluster and dried bulbs per plot (tonnes per ha bulbs) (Saharuddin et al. 2018).
Also, Rhizobium is used as biofertilizer in agriculture to promote plant development as an addition to chemical fertilizers. Microorganisms that can dissolve potassium have been utilized as cyanobacteria, nitrogen-fixing bacteria, phosphate mineralizing bacteria, and a variety of crops using biofertilizers. Rhizobacteria’s ability to survive in soil is influenced by a variety of abiotic and biotic factors. The bacteria are mixed with a carrier to improve their rate of survival in soil and to increase their viability and effectiveness (Khosravi and Rahmani 2022.; Negash and Wondimu 2022) (Tables 1 and 2).
Silicate bacteria obviously play a part in the weathering of silicate minerals, but the main degrading factor appears to be the formation of acids by the microbes that live on stone. It is believed that heterotrophic bacteria and fungus secrete organic acids like oxalic, citric, or gluconic acids, which are more significant weathering agents. The effectiveness of two strains of B. circulans and one strain of Arthrobacter tumescens, silicate bacteria, in mobilizing potassium from certain aluminsilicates (orthoclase, microcline, mica-mucovite, and nile silt). These silicate bacteria clearly enhanced the weathering of the studied materials, mobilizing significant quantities of potassium. Due to physical and chemical degradation, the aseptic incubation of moist silicate minerals with silicate bacteria gradually increased the levels of soluble and amorphous silica. The order of release of water-soluble silica was micamuscovite, nile silt, microcline, and orthoclase. Muscovite experienced the biggest changes in soluble and amorphous aluminum content, while silt experienced the least changes. The dissolution of all the silicate minerals was positively impacted by nitrogen amendment, which indirectly increases soil fertility by raising the percentage of clay and minerals (Raturi et al. 2021; Afify 2022).
Algae as biofertilizers
The best substitutes for synthetic fertilizers are biofertilizers. Algal species hold considerable promise for biofertilizer technology in terms of affordability and environmental friendliness (Chatterjee et al. 2017). The algal pathway provides significant byproducts, and its effectiveness as a biofertilizer is its physicochemical behavior, and that soil health is enhanced. Algae are the most advantageous and in-demand bio resource of the twenty-first century due to their technological and commercial viability and environmental advantages (Mahapatra et al. 2018) (Fig. 3).
Microalgae as biofertilizer
Eukaryotic green algae and prokaryotic blue algae are common photosynthetic microalgae. Due to their capacity to improve macro- and micronutrient consumption and enrich soil nutrients, they offer significant potential for use in modern agriculture. Microalgae can create plant growth hormones, polysaccharides, antimicrobial compounds, and other metabolites to support plant growth in addition to enhancing soil fertility and quality (Guo et al. 2020). Microalgae are an important source of biofertilizers for agriculture (Dineshkumar et al. 2019). The bioactivities and physicochemical characteristics of microalgal generated extracts (bioactive and high-value products) are used to classify them. Microalgae offer a number of advantageous qualities. Due to the inherent bioactive chemicals that increase plant productivity, they have received widespread recognition for agricultural uses (Bello et al. 2021). Microalgal biofertilizers can replace chemical fertilizers since they are easily renewable, less expensive, and can assist farmers in growing healthy organic crops and fostering an environment free of harmful chemicals (Dineshkumar et al. 2020). In place of artificial fertilizers, cyanobacteria are an effective biofertilizer that promotes plant development and crop production while improving the soil’s quality by adding organic matter to the soil (Maqubela et al. 2009). Additionally, algal biomass is a rich source of metabolites (Renuka et al. 2018; Jamal Uddin et al. 2019) (Table 3).
Algae are plentiful and easy to find in a moist environment. Algae and the substances they produce can aid in the commencement of seed germination and the growth of plant roots, which affects temperature, resilience to abiotic stress, and the capacity of plants to absorb nutrients (Zafar et al. 2022). Algal biofertilizers have potential to reduce synthetic nitrogen fertilizer use. The cyanobacteria may be able to fix up to 22.3–53.1 kg of nitrogen per hectare, which could prevent the need for 25–50% of chemical nitrogen fertilizer (Issa et al. 2014). Algal biofertilizers are able to increase seed germination rate. Winter wheat and cress seed germination were both improved by supercritical fluid extracts of spirulina biomass (Michalak et al. 2016). Also, they have the ability to increase crop yield by enhancing soil fertility, providing plant growth hormones and plant tissue colonization. They improve the quality of fruits and vegetables. Despite some challenges, algae have a promising future as biofertilizers (Table 3).
Macroalgae as biofertilizer
The complex and widely distributed group of photosynthetic organisms known as seaweed is essential to aquatic environments (Egan et al. 2013). The aquatic plant kingdom Thallophyta includes seaweeds, commonly referred to as macroalgae, which are regarded as a vital component of the marine ecology and lives in coastal waters (Nabti et al. 2017). There are thought to be 9000 species of macroalgae. Based on the existence of photosynthetic pigment, storage capacity, and other factors, macroalgae can be divided into three primary groups based on components of food products’ cell walls and include Rhodophyta (red), Phaeophyta (brown), and Chlorophyta (green) (Khan et al. 2009; Zafar et al. 2022). Seaweeds are typically found clinging to the bottom of rather shallow coastal waters. A new generation of natural organic fertilizers called seaweed extract contains an effective nutrient source that encourages faster seed germination, increased crop yield, and increased crop resistance (Selvam and Sivakumar 2013; Suriya et al. 2018). Seaweed extracts enhance biological characteristics of the soil and raise output under biotic and abiotic stress (Yanebis Pérez Madruga 2020). Brown macroalgae, such as Ascophyllum nodosum (L.), are most frequently utilized in agriculture (Khan et al. 2009; Tuhy et al. 2013; Díaz-Leguizamón et al. 2016). In addition to A. nodosum, other brown algae such as Ecklonia maxima (Osbeck) Papenfuss, Fucus spp., Laminaria spp., Sargassum spp., and Turbinaria spp. serve as biofertilizers. Mediterranean red algae like Corralina, Green algae, Pterocladia pinnata (Hudson) Papenfuss, and Jania rubens (L.) J.V. such as Enteromorpha intestinalis (L.) Nees, Cladophora dalmatica Kützing, Ulva lactuca L. is also employed as a biostimulant for plant growth (Aghofack et al. 2015; Mireya Hernández-Herrera et al. 2016; Yanebis Pérez Madruga 2020). Algal extracts and inorganic (Coppens et al. 2016; Ronga et al. 2019; El-Moursy et al. 2019) (Coppens et al. 2016; Salim 2016; Wafaa et al. 2017; Ronga et al. 2019) fertilizers can be combined, which might promote sustainable agricultural productivity. They can be used in various ways, including foliar sprays (Ronga et al. 2019), soil additives (Hashem et al. 2019; Omer et al. 2019), and on seeds (Das et al. 2019; Ronga et al. 2019; Hernández-Herrera et al. 2019). Demonstrating a broad range of applications, many beneficial effects are found, such as improved germination, radicular system development, better fruit quality, increased leaf area and chlorophyll content, improved crop output, vitality, strong resilience to biotic and abiotic stress, and extended postharvest shelf-life products (Khan et al. 2009; El-Baky et al. 2010; Paudel et al. 2012; Guzmán-Murillo et al. 2013; Mireya Hernández-Herrera et al. 2016; Coppens et al. 2016; Oancea et al. 2017; Hernández-Herrera et al. 2018, 2019; Das et al. 2019; Patel et al. 2019; Sunarpi et al. 2019; Hashem et al. 2019; Ronga et al. 2019; El-Moursy et al. 2019). Macroalgae have the ability to increase crop yield, improve seed germination, improve soil characteristics, increase growth and quality of crops, and improve abiotic stress tolerance (Yanebis Pérez Madruga 2020).
Some marine macroalgae are used as biofertilizers by mixing their pulverized form with the soil. They contain unexplored reservoirs of naturally occurring physiologically active chemicals (Nabti et al. 2017). They serve as abundant sustainable botanical bioresources (Khan et al. 2009). Due to their high quantities of organic matter, which enriches soil with nutrients, marine macroalgae are effective biofertilizers (Kumareswari and Rani 2015; Layek et al. 2018). Additionally, when applied in sufficient amounts, they were superior and a more acceptable alternative to chemical and mineral fertilizers (Mirparsa et al. 2016). Marine macroalgae have numerous uses as eco-friendly fertilizers in contemporary agriculture and horticulture crop enhancement (in finely powdered form) (Hernández-Herrera et al. 2018). The application of seaweed as a soil amendment was effective on enhancing plant growth (Hernández-Herrera et al. 2014; Hashem et al. 2019). Many parts of the world employ seaweed manure to improve in agricultural soil (Eyras et al. 2013; Ramya et al. 2015) (Table 4).
While, another marine macroalgae are used as liquid biofertilizers and are sprayed over the soil and plants. Due to their high levels of organic matter, micro and macro elements, vitamins, and other nutrients, liquid fertilizers made from natural sources, such as seaweed, are effective fertilizer alternatives for agricultural crops. Fatty acids and growth regulators are abundant (Crouch and vanStaden 1993). In agriculture and horticulture, bioactive compounds derived from marine algae are used, and numerous positive results in terms of improvement to productivity and quality have been observed (Crouch and vanStaden 1993; Blunden et al. 1996; Suriya et al. 2018). Seaweed extracts have the potential to replace chemical fertilizers with environmentally friendly liquid biofertilizers, which is essential for organic agricultural techniques leading to sustainable agriculture (Ramya et al. 2015). A variety of liquid fertilizers from seaweed are applied as a foliar spray (Thirumaran et al. 2009; Ramya et al. 2015) (Table 5).
Fungi as biofertilizer
Fungi are one of the most significant taxonomic families of eukaryotic and heterotrophic living organisms on Earth and include mildew, mold, mushrooms, yeast, and puffballs They are advantageous for crop protection, plant growth, and crop yield (Arora 2019; Devi et al. 2020; Ahmad et al. 2022).
In order to enhance, add, conserve, and transform nutrients from an unusable form to a usable form, biofertilizers are made of biologically active bacterial and fungal strains (Rastegari et al. 2020a, b). Helpful fungi benefits the plant by producing siderophores, gluconase antagonists, antibiotics, and cell wall lysing enzymes like cellulases and glycosidase, among other directed multifarious plant growth-promoting characteristics. Micronutrients (phosphorus, potassium, and zinc) are also solubilized, and auxin, gibberellins, cytokinin, and ethylene are produced (Arora 2019; Abo Nouh 2019; Devi et al. 2020; Ahmad et al. 2022).
Micro fungi as biofertilizers
Globally, the use of chemical fertilizers in agriculture has significantly increased over the past two decades, but excessive fertilizer use is having increasingly negative effects on the environment of the soil and water bodies. As a result, the idea of using mycorrhizal fungi as a biofertilizer is a promising one from the perspectives of cost effectiveness, energy conservation, and environmental friendliness (Nath Yadav and Yadav 2020; Kour et al. 2020; Thakur 2020). Mycorrhiza is a massive, useful, and underutilized resource for soil ecosystem management. It is a diverse group of fungi that is mostly found on the roots of plants (Singh et al. 2019; Nath Yadav and Yadav 2020; Kour et al. 2020; Thakur 2020). Biofertilizers are broadly classified as N2 fixing (free-living, symbiotic, and associative symbiotic), phosphate solubilizing (bacteria and fungi), phosphate mobilizing (arbuscular mycorrhiza, ecto mycorrhiza, ericoid mycorrhizae, orchid mycorrhiza, and plant growth-promoting rhizobacteria) (Rastegari et al. 2020b). After nitrogen, phosphorus is the second-most crucial macronutrient for plants (Arora 2019; Devi et al. 2020; Ahmad et al. 2022). The amount of soluble phosphorus in soil is insufficient for plants’ metabolic processes, and a shortfall could result in slower development and decreased leaf biomass, (Arora 2019; Devi et al. 2020; Ahmad et al. 2022). Several chemical fertilizers were used to meet the shortfall but were harmful to the environment. As a result, fungi are considered as an alternative strategy, because fungi are naturally occurring organisms that provide soluble phosphorus without endangering the environment (Arora 2019; Devi et al. 2020; Ahmad et al. 2022). Plants obtain phosphorus from the earth in the form of phosphate. In comparison to other macronutrients, this element has very little mobility in the plant. Phosphorus-soluble microorganisms play an important role in phosphorus-based nutrition, increasing plant supply by releasing organic and mineral soil phosphorus pools via solvent and mineralization (Abo Nouh 2019; Aslam et al. 2022) (Table 6), while potassium is the most abundant macronutrient and is essential for plant growth and development. The most significant component of microbial communities in soil, particularly in the rhizosphere, is potassium, which is used to solubilize minerals rich in potassium. In particular, two useful communities of the arbuscular mycorrhizal fungus G. intraradices and G. mosseae could be incorporated into the soil as inoculants to promote the growth of crops (Arora 2019; Devi et al. 2020; Ahmad et al. 2022) (Table 6).
There are five stable isotopes of zinc (Zn), which is the 23rd most plentiful element on earth (Arora 2019; Devi et al. 2020; Ahmad et al. 2022). Zinc is a key component of many metabolic processes and functions as a regulatory cofactor for enzymes and proteins. It is well known that the structural motif of the zinc finger plays a key function in the control of transcription (Arora 2019; Devi et al. 2020; Ahmad et al. 2022). Fungi create organic acids that increase the mobilization of zinc by changing its insoluble form to soluble, which is easily accessible in soil (Arora 2019; Devi et al. 2020; Ahmad et al. 2022). The potential to dissolve zinc has been seen in ericoid mycorrhiza, including Suillus bovinus, Suillus luteus, Paxillus involutus, Oidiodendron maius, Hymenoscyphus ericae, and Beauveria caledonica (Arora 2019; Devi et al. 2020; Ahmad et al. 2022) (Haro and Benito 2019) (Fig. 4, Table 6).
Macro fungi as biofertilizers
A collection of microbiomes that interact with plant roots affects plant development and defense. Numerous bacteria, fungi, actinomycetes, and other eukaryotic microorganisms can be cultivated in microbiomes. Rhizobacteria are the bacteria that live in the rhizosphere and improve plant development and crop yield. The most essential plant growth-promoting fungi are Penicillium, Trichoderma, Fusarium, and Phoma. The cucumber has developed systemic resistance to many diseases due to the presence of many plant growth-promoting fungi species (Romera et al. 2019). These fungi are non-pathogenic saprophytes that live in soil and aid crop plants by protecting them from disease as well as boosting plant growth (Begum et al. 2019) (Table 7).
The non-pathogenic Fusarium species effectively promote plant growth. Competition and induction of host defenses follow two possible modes of action. There have been numerous reports of non-pathogenic Fusarium oxysporum strains controlling Fusarium wilt in various crops (El-Maraghy et al. 2020). Phoma sp. and P. simplicissimum are fungi that encourage plant growth and successfully stimulated cucumber systemic resistance to the anthracnose-causing organism Colletotrichum orbiculare. Results from the controlled cultivation of Piriformospora indica (Hymenomycetes: Basidiomycota) revealed that the species was an endophyte and stimulated plant growth (Begum et al. 2019). Vesicular–arbuscular (VA) mycorrhiza are used in biofertilizers as nutrient mobilizers and Trichoderma spp. are used as cellulose decomposers (Kar et al. 2021). Other species used as biofertilizers include Aspergillus awamori, A. niger, and Penicillium digitatum, which are phosphate solubilizers, and contribute to processes like respiration, photosynthesis, energy transfer, signal transduction, energy accumulation, cell enlargement, cell division, and macromolecular biosynthesis. Lowering soil pH through microbial generation of organic acids or the release of protons is the main mechanism for solubilizing soil phosphorus (Babalola et al. 2021). Phosphorus can precipitate in alkaline soils to create calcium phosphates, such as rock phosphate (fluorapatite and francolite), which are insoluble in the ground. As the pH of the soil lowers, their solubility rises. Phosphorus solubilizing microorganisms produce organic acids that reduce the pH of the soil, increasing the availability of phosphorus. The production of organic acids and the solubility index are strongly positively correlated. By releasing CO2, phosphorus solubilizing microorganisms are also known to produce acidity, as seen in the calcium phosphates’ solubility. Phosphorus was dissolved as a result of the production of organic acid and the pH drop caused by the action of microbes. Many fungi such as Penicillium bilaii, Penicillium citrinum, Trichoderma viride, Aspergillus sydawi, and Aspergillus tubingensis have this mechanism (Kalayu 2019) (Table 7).
Despite having an adequate total Zn concentration, insoluble Zn in the soil contributes to Zn deficiency in plants. While Zn is immobile in poorly reducing neutral or alkaline soils, it is easily transportable into plants in oxidizing acidic soil. Zn is transported in the soil solution by mass flow, diffusion, and root extension in the direction of the roots whether it is a divalent cation or complexed with ligand via several transporter systems. The active transport system, which moves Zn from the root to the shoots, is responsible for the majority of Zn absorption. The basal node retains a small amount of zinc, which controls the amount of zinc distributed throughout plants. Some fungi can solubilize insoluble Zn and include Penicillium luteum, Aspergillus niger, A. nomius, A. oryzae, Trichoderma harzianum rifai, and Beauveria caledonica (Rani et al. 2020) (Table 7).
Vesicular–arbuscular mycorrhiza interact with other microorganisms in the rhizosphere and are one of the significant soil microorganisms. Under field conditions, VA mycorrhiza inoculation significantly increased growth of transplanted chilies. Vesicular–arbuscular mycorrhiza aid in the uptake of Zn, Cu, Fe, Mn, and other nutrients by expanding the network of hyphae in their cells. By entangling soil particles and organic components to form a skeletal framework of macro aggregates, VA mycorrhiza hyphae play a significant role in soil aggregation. These aggregates improve the storage of carbon and nutrients and provide a favorable habitat for the survival and development of soil microorganisms. In organic and sustainable farming systems that rely on biological processes rather than agrochemicals to prevent plant diseases, VA mycorrhiza are particularly crucial. Plants are biologically protected by VA mycorrhiza from soil-borne diseases, including Aphanomyces, Cylindrocladium, Fusarium, Macrophomina, Phytophthora, Pythium, Rhizoctonia, Sclerotinium, Verticillium, and Thielaviopsis sp. (Dubey et al. 2019). A study showed that by producing organic acids including malate, citrate, and oxalate as well as protons, H+, and CO2, arbuscular mycorrhizal fungi improved the availability of K. Dual inoculation of maize with G. intraradices and G. mosseae improved K absorption, and K solubilizing microorganisms promoted the growth of cotton, rape, pepper, cucumber, khella, sorghum, wheat, tomato, chili, Sudan grass, and tobacco (Mącik et al. 2020) (Table 7).
Plant residues as biofertilizers
Plants are like all living organisms can be used as biofertilizers by using the unused parts of them (plant residues) for manufacturing of ecofriendly biodegradable fertilizers. Plant residues are used as soil biofertilizers and include banana peels. Banana is a popular fruit, because of its taste and nutritional value. As a result, large quantities of banana peel by-products are obtained. Studies have shown that the content of bananas, such as the peel and bloom, is rich in macro- and micronutrients and promotes good health through its anti-inflammatory and anti-oxidative stress properties. Research to transform banana peels into unique new items due to their benefits like increasing soil fertility is ongoing (Kraithong and Issara 2021) (Table 8). According to the international biochar initiative (2012), banana peel biochar is a carbon-rich product that is described as “a solid compound generated through the thermo-chemical conversion of biomass in an oxygen-constrained environment” (Novak et al. 2012), (Islam et al. 2019), (Comino et al. 2020). Due to its distinctive characteristic, which enhances soil quality, banana peel biochar has recently taken center stage in research (Novak et al. 2012), (Islam et al. 2019), (Comino et al. 2020) (Table 8).
Biochar is produced using a variety of agricultural and forestry wastes, including nutshells, rice husk, pinewood, and orchard pruning biomass (Carter et al. 2013; Thornbro 2022). Banana (Musa sapientam L.), one of the most commercially significant fruit crops in Bangladesh, is produced at household and commercial scale in around one million tons per year (Hossain 2014). When compared to other fruit crops, it is widely consumed and accessible all year round in Bangladesh. The peel of a banana, which is regarded as waste, makes up around 18–20% of its body weight (Chenost et al. 1976) (Table 8). Banana peel waste was converted into biochar using a slow pyrolysis technique with little oxygen. Three replications of each of three rates (1, 2, and 3%) of banana peel biochar were applied to agricultural soil. K concentration in banana peel biochar was high. Compared to controls, plant production and above-ground biomass decreased in 1% banana peel biochar treatments but increased in 2 and 3% treatments. Additionally, plants cultivated with banana peel biochar were stronger, healthier, and more attractive. So, for sustainable agriculture, banana peel biochar may be an excellent source of K amendment and be used in place of chemical fertilizer as a supply of K (Islam et al. 2019) (Table 8). A popular beverage consumed worldwide is coffee (Obruca et al. 2015), and during the past several decades, wastes such as spent coffee grounds (SCG) and coffee waste, which are typically disposed of with regular trash, have expanded significantly (Mussatto et al. 2011) (Cruz et al. 2012). These are the main coffee waste by-products (45%) produced during the manufacture of instant coffee and the preparation of drinks, such as the espresso coffee extraction process (Murthy and Madhava Naidu 2012; Chrysargyris et al. 2021). Coffee grounds are used to produce biochar and as a low-cost adsorptive material for the biosorption of heavy metals (Cd, Cr, Cu, and Pb) from aqueous solutions (Kyzas 2012); (Davila-Guzman et al. 2016). The composition of SCG makes it possible to use it as soil organic amendment. Studies reveal that SCG has positive effects since it increased nitrogen, phosphorous, potassium, and organic carbon content in soils (Yamane et al. 2014; Cervera-Mata et al. 2018; Comino et al. 2020). However, huge loads of SCG deposited into landfills may contaminate water supplies, emit CO2, and hinder plant development (Murthy and Madhava Naidu 2012; Chrysargyris et al. 2021). Due to its poisonous nature for seedling growth, SCG is rarely used as fertilizer (Ciesielczuk et al. 2019). It is advised that SCG be combined with ash from thermal biomass treatment for golden rods (Solidago canadensis L.).
The effect of SCG on three brassica species, namely cauliflower F1 Skywalker (Brassica oleracea L. var. botrytis), broccoli F1 Marathon (Brassica oleracea L. var. cymosa), and cabbage F1 Paltar (Brassica oleracea L. var. capitata) was studied. It was found that SCG changed the physicochemical properties of growth media by increasing media bulk density and mineral components, which was accessible while lowering available porosity. Although stomatal conductance, one of the physiological characteristics of plants, was lowered, the SCG in the substrate had an impact on the mineral accumulation in plants, causing levels of nitrogen, potassium, phosphorus, and copper to rise (Chrysargyris et al. 2021). Spent coffee grounds have the potential to increase soil fertility, and further investigations are needed to improve the use of SCG as an amendment (Cervera-Mata et al. 2018) (Table 8).
Pomegranates are one of three fruits eaten the most over the world. Pomegranate output worldwide was predicted to be 3.8 million metric tons in 2017. Pomegranate peel accounts for 26–30% of the fruit’s weight and contains significant amounts of phenolic chemicals, such as flavonoids and hydrolyzable tannins, as well as 92% antioxidant activity (el Barnossi et al. 2021). Pomegranate fruit peel contains K, N, Ca, P, Mg, and Na, as well as B, Fe, ZN, Cu, and Mu as micronutrients (Dayarathna and Karunarathna 2021). The peels also contain amino acids, vitamins, phenolic compounds, flavonoids, anthocyanins, and tannins (Omer et al. 2019). Peel from a pomegranate is regarded as an organic fertilizer. To substitute chemical fertilizers with organic wastes, the effects of pomegranate peel formulations (powder, water extract, and ethanol extract) on the growth and chemical composition of sage were assessed. During the second harvest, 6 g/L (water extract) produced the highest fresh mass (68.5 g/plant), dry mass (18 g/plant), essential oil content (1.6%, v/w), and essential oil production (28.8 ml/100 plants) values. The peel accounted for around 500 g/kg of the overall fruit weight (Aviram et al. 2000). Pomegranate powder was effectively composted by combining, it with and without banana peels at a humidity level of 50 5%. Digestion took 15 days, and the C:N ratio dropped from 22.5 to 17. The biofertilizer created using both of these techniques enhanced germination, shoot development, root length, and leaf chlorophyll content. The biofertilizers boosted yield and phenolic acid levels in wheat grains when compared to chemical farming (Singh et al. 2013; el Barnossi et al. 2021). Thus, pomegranate peel can be considered to be an organic fertilizer (Pathak et al. 2017).
Grass pea is grown as a summer crop in Kashmir and Nepal and as a winter crop in low-lying areas, such as Bangladesh (Girma and Korbu 2012). Due to its effectiveness in fixing nitrogen, grass pea is a good green manure that increases soil fertility by adding around 67 kg/ha of additional nitrogen in a single growing season. This holds advantages for subsequent non-legume crops in terms of productivity and protein (Singh et al. 2013). Cool season legumes are the key to sustainable agriculture because they are sown in the winter, extending the growth season of cereal crops and replenishing the soil with vital nitrogen and other nutrients. Farmers in Australia observed a 30% increase in wheat production compared to mono cropped wheat after using a legume rotation (Stagnari et al. 2017). Studies from Denmark also show that during rotations with field pea and lupin, the absorption of nitrogen by a variety of crops rises by 23–59% (Stagnari et al. 2017). This legume-mediated improvement in nitrogen use efficiency offers a sustainable and cost-effective alternative to high-input fertilizer regimes because N is one of the most restricting nutrients for cereal and crop productivity. Due to pea nodules, which need P for the transformation of energy, field pea and legumes in general are problematic for sustainable agriculture since they require substantially more P input than other crops (Lambein et al. 2019) (Table 8).
Generally, pulses are highly advantageous to farming systems and have had great success in sustainable farming systems through intercropping and crop rotation with cereals. In addition to replenishing soil nitrogen through their capacity to fix N from the atmosphere via nodules and symbiotic relationships with rhizobia, pulses can disrupt disease, weed cycles linked to cereals, raising soil organic carbon, water retention and reducing greenhouse gas emission (Foyer et al. 2016; Stagnari et al. 2017; Peoples et al. 2019)(Powers and Thavarajah 2019) (Table 8).
Future Prospects
The use of biofertilizers is unquestionably the future of agriculture where it is anticipated to take the place of chemical fertilizers. It aids the process and protects soil biodegradation performed by living things, which ultimately results in a safe technique to boost soil fertility without using chemicals residues. Additionally, we anticipate adding nanomaterials to biofertilizers could offer eco-friendly and effective substitutes. Therefore, plant diseases could be controlled and plant resistance increased to reduce environmental stress and boost plant productivity and quality.
Using simulation systems in smart agriculture for each crop and its methods like using IoT applications, Big data, and cloud computing, artificial intelligence techniques are used to study plant diversity in various regions and determine the biofertilizers needed to stimulate a species’ growth and which organisms are best at extracting this biofertilizer.
Promoting the dissemination of the culture of using biofertilizers among farmers through voluntary awareness campaigns and conducting questionnaires to assess their understanding and clarify the importance of biofertilizers over chemical fertilizers, especially in agricultural areas that are still virgin in their natural habitat, such as North Africa, East Asia, the Caribbean, and some Latin American countries through support Micro-innovative projects based on the idea of entrepreneurship to produce vital local fertilizers from their environment and support them at a lower cost for farmers commercially such as microbial biostimulants and biofilm-based biofertilizers.
Conclusion
New environmentally friendly technologies include the use of biofertilizers that will be part of sustainable agriculture. Because of its increased nutrient content, biofertilizers enhance soil fertility and increase plant productivity. It is possible to obtain biofertilizers from a variety of organisms. These include microorganisms such as bacteria (Azotobacter, Cyanobacter, and Nitrobacter), microalgae (Chlorella vulgaris, Spirulina platensis, Haematococcus pluvialis, and Acutodesmus dimorphus), and micro fungi (Glomus spp.) Also residues of macro organisms either algae, fungi, or plants can be used as biofertilizers. In addition to their biodegradable nature, the microorganisms and residues of macro organisms can safely increase soil fertility without accumulating contaminants, which preserves the integrity of the environment and its ecosystems, so this supports the principles of sustainable development.
Data availability
Available via corresponding author.
References
Abd El-Aal AAM (2022) Anabaena-azollae, significance and agriculture application: a case study for symbiotic cyanobacterium. Microb Syntrophy-Mediated Eco-Enterprising 1–14. https://doi.org/10.1016/B978-0-323-99900-7.00006-7
Abdelsalam IM, Ghosh S, AlKafaas SS et al (2022) Nanotechnology as a tool for abiotic stress mitigation in horticultural crops. Biologia 78(1):163–178. https://doi.org/10.1007/S11756-022-01251-Z
Abd-Rabbu HS, Wahba HE, Khalid KA (2021) Pomegranate peel modifies growth, essential oil and certain chemicals of sage (Salvia officinalis L.) herb. Biocatal Agric Biotechnol 33:101978. https://doi.org/10.1016/J.BCAB.2021.101978
Abo Nouh FA (2019) Endophytic fungi for sustainable agriculture. Microbial Biosystems 4:31–44. https://doi.org/10.21608/MB.2019.38886
Adhikari K, Bhandari S, Acharya S (2020) An overview of Azolla in rice production: a review. Rev Food Agric 2:04–08. https://doi.org/10.26480/rfna.01.2021.04.08
Afify AH (2022) Review article silicate bacteria as a biofertilizer. J Agric Chem Biotechnol 13:75–83. https://doi.org/10.21608/JACB.2022.154996.1029
Aghofack J, Schinzoumka P, Tatchago V (2015) Effets des extraits ou de la poudre de Spirulina platensis et Jatropha curcas sur la croissance et le développement de la tomate. ajol.info. J Appl Biosci https://doi.org/10.4314/jab.v90i1.2
Ahmad F, Saeed Q, Shah SMU et al (2022) Environmental sustainability: challenges and approaches. Nat Resour Conserv Adv Sustain 243–270. https://doi.org/10.1016/B978-0-12-822976-7.00019-3
Aioub AAA, Elesawy AE, Ammar EE (2022) Plant growth promoting rhizobacteria (PGPR) and their role in plant-parasitic nematodes control: a fresh look at an old issue. J Plant Dis Prot 2022:1–17. https://doi.org/10.1007/S41348-022-00642-3
Alori ET, Babalola OO (2018) Microbial inoculants for improving crop quality and human health in Africa. Front Microbiol 9:2213. https://doi.org/10.3389/FMICB.2018.02213
Ammar EE, Aioub AAA, Elesawy AE et al (2022) Algae as bio-fertilizers: between current situation and future prospective. Saudi J Biol Sci 29:3083–3096. https://doi.org/10.1016/J.SJBS.2022.03.020
Ammar E (2022) Environmental impact of biodegradation. Handb Biodegradable Mater 1–40. https://doi.org/10.1007/978-3-030-83783-9_27-1
Arora PK (2019) Microbial metabolism of xenobiotic compounds. 2512-1898, 1(XIII):357, Springer. https://doi.org/10.1007/978-981-13-7462-3
Aslam AA et al (2022) Applications of Microbes in Soil Health Maintenance for Agricultural Applications. In: Inamuddin, Ahamed MI, Prasad R (eds) Application of Microbes in Environmental and Microbial Biotechnology. Springer, Singapore. https://doi.org/10.1007/978-981-16-2225-0_12
Aviram M, Dornfeld L, Rosenblat M et al (2000) Pomegranate juice consumption reduces oxidative stress, atherogenic modifications to LDL, and platelet aggregation: studies in humans and in atherosclerotic apolipoprotein E–deficient mice. Am J Clin Nutr 71:1062–1076. https://doi.org/10.1093/AJCN/71.5.1062
Babalola OO, Seenivasagan R, Alexandre A, Wippel K (2021) Utilization of microbial consortia as biofertilizers and biopesticides for the production of feasible agricultural product. Biology 10:1111. https://doi.org/10.3390/biology10111111
Backer R, Rokem JS, Ilangumaran G et al (2018) Plant growth-promoting rhizobacteria: context, mechanisms of action, and roadmap to commercialization of biostimulants for sustainable agriculture. Front Plant Sci 1473. https://doi.org/10.3389/FPLS.2018.01473/FULL
Bao J, Zhuo C, Zhang D et al (2021) Potential applicability of a cyanobacterium as a biofertilizer and biopesticide in rice fields. Plant Soil 463:97–112. https://doi.org/10.1007/S11104-021-04899-9
Bedair H, Ghosh S, Abdelsalam IM et al (2022a) Potential implementation of trees to remediate contaminated soil in Egypt. Environ Sci Pollut Res 29(52):78132–78151. https://doi.org/10.1007/S11356-022-22984-Z
Bedair H, Rady HA, Hussien AM et al (2022b) Pesticide detection in vegetable crops using enzyme inhibition methods: a comprehensive review. Food Anal Methods 15(7):1979–2000. https://doi.org/10.1007/S12161-022-02254-X
Begum N, Qin C, Ahanger MA et al (2019) Role of arbuscular mycorrhizal fungi in plant growth regulation: implications in abiotic stress Tolerance. Front Plant Sci 10:1068. https://doi.org/10.3389/FPLS.2019.01068/FULL
Bello AS, Saadaoui I, Ben-Hamadou R (2021) “Beyond the source of bioenergy”: microalgae in modern agriculture as a biostimulant, biofertilizer, and anti-abiotic stress. Agronomy 11:1610. https://doi.org/10.3390/AGRONOMY11081610
Beneduzi A, Peres D, Vargas LK et al (2008) Evaluation of genetic diversity and plant growth promoting activities of nitrogen-fixing bacilli isolated from rice fields in South Brazil. Appl Soil Ecol 39:311–320. https://doi.org/10.1016/J.APSOIL.2008.01.006
Bhardwaj D, Ansari MW, Sahoo RK, Tuteja N (2014) Biofertilizers function as key player in sustainable agriculture by improving soil fertility, plant tolerance and crop productivity. Microb Cell Fact 13:1–10. https://doi.org/10.1186/1475-2859-13-66
Bhuyan PP, Nayak R, Jena M, Pradhan B (2022) Convoluted role of cyanobacteria as biofertilizer: an insight of sustainable agriculture. Vegetos 2022:1–13. https://doi.org/10.1007/S42535-022-00415-1
Blunden G, Jenkins T, Liu YW (1996) Enhanced leaf chlorophyll levels in plants treated with seaweed extract. J Appl Phycol 8:535–543. https://doi.org/10.1007/BF02186333
Bulinski A, Butkovsky O, Sadovnichy V et al (2012) Statistical methods of SNP data analysis and applications. Open J Stat 02:73–87. https://doi.org/10.4236/OJS.2012.21008
Carter S, Shackley S, Sohi S et al (2013) The impact of biochar application on soil properties and plant growth of pot grown lettuce (Lactuca sativa) and cabbage (Brassica chinensis). Agronomy 3(2):404–418. https://doi.org/10.3390/agronomy3020404
Cervera-Mata A, Pastoriza S, Rufián-Henares JÁ et al (2018) Impact of spent coffee grounds as organic amendment on soil fertility and lettuce growth in two Mediterranean agricultural soils. Arch Agron Soil Sci 64:790–804. https://doi.org/10.1080/03650340.2017.1387651
Chatterjee A, Singh S, Agrawal C et al (2017) Role of algae as a biofertilizer. Algal Green Chem: Recent Prog Biotechnol 189–200. https://doi.org/10.1016/B978-0-444-63784-0.00010-2
Chenost M, Geoffroy F, Bousquet P, Candau M (1976) Possibilities of using bananas for feeding of ruminants in humid tropical region. J Agric P R 60:516–525
Chrysargyris A, Antoniou O, Xylia P et al (2021) The use of spent coffee grounds in growing media for the production of Brassica seedlings in nurseries. Environ Sci Pollut Res 28:24279–24290. https://doi.org/10.1007/S11356-020-07944-9
Chungopast S, Thongjoo C, Islam AKMM, Yeasmin S (2021) Efficiency of phosphate-solubilizing bacteria to address phosphorus fixation in Takhli soil series: a case of sugarcane cultivation, Thailand. Plant Soil 460:347–357. https://doi.org/10.1007/S11104-020-04812-W
Ciesielczuk T, Rosik-Dulewska C, Poluszynska J, Slezak E (2019) Assessment of effectiveness of organo-mineral fertilizer made of coffee spent grounds and biomass ash. J Ecol Eng 20:73–78. https://doi.org/10.12911/22998993/96269
Comino F, Cervera-Mata A, Aranda V et al (2020) Short-term impact of spent coffee grounds over soil organic matter composition and stability in two contrasted Mediterranean agricultural soils. J Soils Sediments 20:1182–1198. https://doi.org/10.1007/S11368-019-02474-5
Coppens J, Grunert O, van den Hende S et al (2016) The use of microalgae as a high-value organic slow-release fertilizer results in tomatoes with increased carotenoid and sugar levels. Springer 28:2367–2377. https://doi.org/10.1007/s10811-015-0775-2
Crouch IJ, vanStaden J (1993) Evidence for the presence of plant growth regulators in commercial seaweed products. Plant Growth Regul 13(1):21–29. https://doi.org/10.1007/BF00207588
Cruz R, Baptista P, Cunha S et al (2012) Carotenoids of Lettuce (Lactuca sativa L.) grown on soil enriched with spent coffee grounds. Mol 17:1535–1547. https://doi.org/10.3390/MOLECULES17021535
Daniel AI, Fadaka AO, Gokul A et al (2022) Biofertilizer: the future of food security and food safety. Microorganisms 10(6):1220. https://doi.org/10.3390/microorganisms10061220
Dar S, Bhat R, Dervash M et al (2021) Azotobacter as biofertilizer for sustainable soil and plant health under saline environmental conditions. Sustain Continuum Plant Soil Health 231–254. https://doi.org/10.1007/978-3-030-48771-3_14
Das P, Khan S, Chaudhary A et al (2019) Potential applications of algae-based bio-fertilizer. Biofertilizers Sustain Agric Environ 41–65. https://doi.org/10.1007/978-3-030-18933-4_3
Davila-Guzman NE, Cerino-Córdova FJ, Loredo-Cancino M et al (2016) Studies of adsorption of heavy metals onto spent coffee ground: equilibrium, regeneration, and dynamic performance in a fixed-bed column. Int J Chem Eng 2016. https://doi.org/10.1155/2016/9413879
Dayarathna SGARM, Karunarathna B (2021) Effect of different fruit peel powders as natural fertilizers on growth of Okra (Abelmoschus esculentus l.). J Agric Sci - Sri Lanka 16:67–79. https://doi.org/10.4038/jas.v16i1.9184
Deepak B, Mohammad WA, Sahoo RK, Narendra T (2015) Plant biostimulants: definition, concept, main categories and regulation. Sci Hortic 196:3–14. https://doi.org/10.1016/J.SCIENTA.2015.09.021
Demoling F, Figueroa D, Bååth E (2007) Comparison of factors limiting bacterial growth in different soils. Soil Biol Biochem 39(10):2485–2495
Devi R, Kaur T, Kour D et al (2020) Beneficial fungal communities from different habitats and their roles in plant growth promotion and soil health. Microbial Biosystems 5:21–47. https://doi.org/10.21608/MB.2020.32802.1016
Díaz-Leguizamón JJ, Chingaté-Cruz OF, Sánchez-Reinoso AD, Restrepo-Díaz H (2016) The effect of foliar applications of a bio-stimulant derived from algae extract on the physiological behavior of lulo seedlings (Solanum quitoense cv. Septentrionale). Cienc Investig Agrar 43:25–37. https://doi.org/10.4067/S0718-16202016000100003
Dineshkumar R, Subramanian J, Gopalsamy J et al (2019) The impact of using microalgae as biofertilizer in maize (Zea mays L.). Waste Biomass Valori 10:1101–1110. https://doi.org/10.1007/s12649-017-0123-7
Dineshkumar R, Subramanian J, Arumugam A et al (2020) Exploring the microalgae biofertilizer effect on onion cultivation by field experiment. Waste Biomass Valori 11:77–87. https://doi.org/10.1007/s12649-018-0466-8
Dubey M, Verma V, Barpete R, Verma N (2019) Effect of biofertilizers on growth of different crops: a review. Plant Arch 19:1083–1086
Egan S, Harder T, Burke C et al (2013) The seaweed holobiont: understanding seaweed-bacteria interactions. FEMS Microbiol Rev 37:462–476. https://doi.org/10.1111/1574-6976.12011
el Barnossi A, Moussaid F, Iraqi Housseini A (2021) Tangerine, banana and pomegranate peels valorisation for sustainable environment: a review. Biotechnol Rep 29:e00574. https://doi.org/10.1016/J.BTRE.2020.E00574
El-Baky HHA, El-Baz FK, Baroty GSE (2010) Enhancing antioxidant availability in wheat grains from plants grown under seawater stress in response to microalgae extract treatments. J Sci Food Agric 90:299–303. https://doi.org/10.1002/JSFA.3815
El-Maraghy S, Tohamy T, Hussein K (2020) Expression of SidD gene and physiological characterization of the rhizosphere plant growth-promoting yeasts. Heliyon 6(7). https://doi.org/10.1016/J.HELIYON.2020.E04384
El-Moursy R, Abido W, Badawi M (2019) Response of maize productivity to nitrogen fertilizer and spraying with blue green algae extract. Int J Agro Agri Res 14(2):10–20
Eyras M, Rostagno C, Defossé G (2013) Biological evaluation of seaweed composting. Compost Sci Utilization 6:74–81. https://doi.org/10.1080/1065657X.1998.10701943
Fikadu O (2022) The response of faba bean (Vicia faba L.) to different strains of rhizobium biofertilizer (Rhizobium leguminosarum) at Horro District, Western Oromia. Int J Appl Agric Sci 8:150–155
Foyer CH, Lam HM, Nguyen HT et al (2016) Neglecting legumes has compromised human health and sustainable food production. Nature plants 2(8):1–10. https://doi.org/10.1038/NPLANTS.2016.112
Garcia-Gonzalez J, Sommerfeld M (2016) Biofertilizer and biostimulant properties of the microalga Acutodesmus dimorphus. J Appl Phycol 28:1051–1061. https://doi.org/10.1007/s10811-015-0625-2
Girma D, Korbu L (2012) Genetic improvement of grass pea (Lathyrus sativus) in Ethiopia: an unfulfilled promise. Plant Breed 131:231–236. https://doi.org/10.1111/J.1439-0523.2011.01935.X
Gören-Sağlam N (2021) Cyanobacteria as biofertilizer and their effect under biotic stress. Plant Growth-Promot Microbes for Sustain Biotic Abiotic Stress. Plant Growth-Promoting Microbes Sustain Biotic Abiotic Stress Manag 485-504. https://doi.org/10.1007/978-3-030-66587-6_18
Guo S, Wang P, Wang X et al (2020) Microalgae as biofertilizer in modern agriculture. Microalgae biotechnology for food, health and high value products 397–411. https://doi.org/10.1007/978-981-15-0169-2_12/COVER
Guzmán-Murillo M, Ascencio F, Larrinaga-Mayoral JA (2013) Germination and ROS detoxification in bell pepper (Capsicum annuum L.) under NaCl stress and treatment with microalgae extracts. Protoplasma 250:33–42. https://doi.org/10.1007/s00709-011-0369-z. (Springer)
Haro R, Benito B (2019) The role of soil fungi in k+ plant nutrition. Int J Mol Sci 20(13):3169. https://doi.org/10.3390/IJMS20133169
Hashem HA, Mansour HA, El-Khawas SA, Hassanein RA (2019) The potentiality of marine macro-algae as bio-fertilizers to improve the productivity and salt stress tolerance of canola (Brassica napus L.) plants. Agronomy 9:146. https://doi.org/10.3390/AGRONOMY9030146
Heba M, El-Beltagi HE-DS, Abd-Elsalam KA (2021) Plant growth-promoting microbes for sustainable biotic and abiotic stress management. Springer International Publishing
Hernández-Herrera RM, Santacruz-Ruvalcaba F, Ruiz-López MA et al (2014) Effect of liquid seaweed extracts on growth of tomato seedlings (Solanum lycopersicum L.). J Appl Phycol 26:619–628. https://doi.org/10.1007/S10811-013-0078-4
Hernández-Herrera RM, Santacruz-Ruvalcaba F, Briceño-Domínguez DR et al (2018) Seaweed as potential plant growth stimulants for agriculture in Mexico. Hidrobiológica 28:129–140
Hernández-Herrera RM, Santacruz-Ruvalcaba F, Hernández-Carmona G (2019) Germination and seedling growth responses of tomato Solanum lycopersicum L. to seaweed extracts applied on seeds. (solabiaa.org) Revista Latinoamericana de Biotecnología Ambiental y Algal 10(1):28-44
Hossain MF (2014) A study of banana production in Bangladesh: area, yield and major constraints. J Agric Biol Sci 9:206–210
Islam M, Halder M, Siddique MAB et al (2019) Banana peel biochar as alternative source of potassium for plant productivity and sustainable agriculture. Int J Recycl Org Waste Agric 8:407–413. https://doi.org/10.1007/S40093-019-00313-8
Issa A, Abd-Alla M, Ohyama T (2014) Nitrogen fixing cyanobacteria: future prospect. Adv Biol Ecol Nitrogen Fixation. https://doi.org/10.5772/56995
Jamal Uddin AFM, Rakibuzzaman M, Wasin EWN et al (2019) Foliar application of Spirulina and Oscillatoria on growth and yield of okra as bio-fertilizer. J Biosci Agric Res 22:1840–1844. https://doi.org/10.18801/jbar.220219.227
Ju X, Zhang F, Bao X et al (2005) Utilization and management of organic wastes in Chinese agriculture: past, present and perspectives. Sci China Ser C: Life Sci 48(2):965–979. https://doi.org/10.1007/BF03187135
Kalayu G (2019) Phosphate solubilizing microorganisms: promising approach as biofertilizers. Int J Agron 2019:1–7. https://doi.org/10.1155/2019/4917256
Kar S, Nehru J, Vishwavidyalaya K et al (2021) Bio-fertilizer in forest nursery-a review. Int J Ind Biotechnol Biomater 6(2):1–14
Khan W, Rayirath UP, Subramanian S et al (2009) Seaweed extracts as biostimulants of plant growth and development. J Plant Growth Regul 28:386–399
Khosravi H, Rahmani HA (2022) Application of rhizobium containing biofertilizers to legume farms (Techniques, potentials, advantages, and limitations). Land Manage J 10(1):95–110
Kinge TR, Ghosh S, Cason ED, Gryzenhout M (2022) Characterization of the endophytic mycobiome in cowpea (Vigna unguiculata) from a single location using illumina sequencing. Agriculture (Switzerland) 12:333. https://doi.org/10.3390/AGRICULTURE12030333/S1
Kour D, Rana KL, Yadav AN et al (2020) Microbial biofertilizers: bioresources and eco-friendly technologies for agricultural and environmental sustainability. Biocatal Agric Biotechnol 23:101487. https://doi.org/10.1016/J.BCAB.2019.101487
Kraithong S, Issara U (2021) A strategic review on plant by-product from banana harvesting: a potentially bio-based ingredient for approaching novel food and agro-industry sustainability. J Saudi Soc Agric Sci 20:530–543. https://doi.org/10.1016/J.JSSAS.2021.06.004
Kumar S, Diksha SSS, Kumar R (2022) Biofertilizers: an ecofriendly technology for nutrient recycling and environmental sustainability. Curr Res Microb Sci 3:100094. https://doi.org/10.1016/J.CRMICR.2021.100094
Kumareswari T, Rani MS (2015) Utilization of seaweeds to enhance growth and nutritive status of Amaranthus caudatus L. Int J Res Stud Biosci (IJRSB) 3:9–15
Kyzas GZ (2012) Commercial coffee wastes as materials for adsorption of heavy metals from aqueous solutions. Materials 5:1826–1840. https://doi.org/10.3390/MA5101826
Lambein F, Travella S, Kuo YH et al (2019) Grass pea (Lathyrus sativus L.): orphan crop, nutraceutical or just plain food? Planta 250:821–838. https://doi.org/10.1007/S00425-018-03084-0
Layek J, Das A, Idapuganti RG et al (2018) Seaweed extract as organic bio-stimulant improves productivity and quality of rice in eastern Himalayas. J Appl Phycol 30:547–558. https://doi.org/10.1007/S10811-017-1225-0
Mącik M, Gryta A, Frąc M (2020) Biofertilizers in agriculture: an overview on concepts, strategies and effects on soil microorganisms. Adv Agron 162:31–87. https://doi.org/10.1016/BS.AGRON.2020.02.001
Mahapatra DM, Chanakya HN, Joshi NV et al (2018) Algae-based biofertilizers: a biorefinery approach. Microorganisms for Green Revolution: Volume 2. Micro Sustain Agro-ecosyst 177-196. https://doi.org/10.1007/978-981-10-7146-1_10
Maqubela MP, Mnkeni PNS, Issa OM et al (2009) Nostoc cyanobacterial inoculation in South African agricultural soils enhances soil structure, fertility, and maize growth. Plant Soil 315:79–92. https://doi.org/10.1007/S11104-008-9734-X
Mei C, Chretien RL, Sajeewa Amaradasa B et al (2021) Characterization of phosphate solubilizing bacterial endophytes and plant growth promotion in vitro and in greenhouse. Microorganisms 9(9):1935. https://doi.org/10.3390/microorganisms9091935
Michalak I, Chojnacka K, Dmytryk A et al (2016) Evaluation of supercritical extracts of algae as biostimulants of plant growth in field trials. Front Plant Sci 7:1591. https://doi.org/10.3389/FPLS.2016.01591/FULL
Mireya Hernández-Herrera R, Santacruz-Ruvalcaba F, Hernandez-Carmona G (2016) Activity of seaweed extracts and polysaccharide-enriched extracts from Ulva lactuca and Padina gymnospora as growth promoters of tomato and mung bean plants. Springer 28:2549–2560. https://doi.org/10.1007/s10811-015-0781-4
Mirparsa T, Ganjali HR, Dahmardeh M (2016) The effect of bio fertilizers on yield and yield components of sunflower oil seed and nut. Int J Agric Biosci 5:46–49
Mishra A, Rajput S, Gupta P et al (2021) Role of cyanobacteria in rhizospheric nitrogen fixation. Soil Nitrogen Ecology. pp 497–519. https://doi.org/10.1007/978-3-030-71206-8_25
Muniswami DM, Chinnadurai S, Sachin M et al (2021) Comparative study of biofertilizer/biostimulant from seaweeds and seagrass in Abelmoschus esculentus crop. Biomass Convers Biorefin. https://doi.org/10.1007/s13399-021-01881-4
Murthy PS, Madhava Naidu M (2012) Sustainable management of coffee industry by-products and value addition—a review. Resour Conserv Recycl 66:45–58. https://doi.org/10.1016/J.RESCONREC.2012.06.005
Mussatto SI, Machado EMS, Martins S, Teixeira JA (2011) Production, composition, and application of coffee and its industrial residues. Food Bioproc Tech 4:661–672. https://doi.org/10.1007/S11947-011-0565-Z
Nabti E, Jha B, Hartmann A (2017) Impact of seaweeds on agricultural crop production as biofertilizer. Int J Environ Sci Technol 14:1119–1134. https://doi.org/10.1007/S13762-016-1202-1
Nath Yadav A, Yadav AN (2020) Plant microbiomes for sustainable agriculture: current research and future challenges. Springer International Publishing 475–482. https://doi.org/10.1007/978-3-030-38453-1_16
Negash H, Wondimu W (2022) Yield maximization of haricot bean by lime, phosphorus and biofertilizer in Ethiopia. Russ Agric Sci 48(3):134–142. https://doi.org/10.3103/S1068367422030065
Nehl DB, Allen SJ, Brown JF (1997) Deleterious rhizosphere bacteria: an integrating perspective. Appl Soil Ecol 5:1–20. https://doi.org/10.1016/S0929-1393(96)00124-2
Nosheen S, Ajmal I, Song Y (2021) Microbes as biofertilizers, a potential approach for sustainable crop production. Sustainability 13:1868. https://doi.org/10.3390/su13041868
Novak JM, Busscher WJ, Watts DW et al (2012) Biochars impact on soil-moisture storage in an ultisol and two aridisols. Soil Sci 177:310–320. https://doi.org/10.1097/SS.0b013e31824e5593
Oancea F, Velea S, Fãtu V et al (2017) Micro-algae based plant biostimulant and its effect on water stressed tomato plants. Rom J Plant Prot 6(2013):104–117
Obruca S, Benesova P, Kucera D et al (2015) Biotechnological conversion of spent coffee grounds into polyhydroxyalkanoates and carotenoids. N Biotechnol 32:569–574. https://doi.org/10.1016/J.NBT.2015.02.008
Omer HAA, Abdel-Magid SS, Awadalla IM (2019) Nutritional and chemical evaluation of dried pomegranate (Punica granatum L.) peels and studying the impact of level of inclusion in ration formulation on productive performance of growing Ossimi lambs. Bull Natl Res Centre 43(1):1–10. https://doi.org/10.1186/S42269-019-0245-0
Pambuka GT, Kinge TR, Ghosh S et al (2021) Baseline data of the fungal phytobiome of three sorghum (Sorghum bicolor) cultivars in south africa using targeted environmental sequencing. J Fungi 7:978. https://doi.org/10.3390/JOF7110978/S1
Pambuka GT, Kinge TR, Ghosh S et al (2022) Plant and soil core mycobiomes in a two-year sorghum–legume intercropping system of underutilized crops in South Africa. Microorganisms 10:2079. https://doi.org/10.3390/MICROORGANISMS10102079/S1
Patel H, Brahmbhatt N, Patel J et al (2019) Effect of seaweed extract on different vegetables as a bio fertilizer in farming. Int J Res 7(3):2062–2067. https://doi.org/10.22214/ijraset.2019.3382
Pathak PD, Mandavgane SA, Kulkarni BD (2017) Valorization of pomegranate peels: a biorefinery approach. Waste Biomass Valor 8:1127–1137. https://doi.org/10.1007/S12649-016-9668-0
Paudel Y, Pradhan S, Pant B et al (2012) Role of blue green algae in rice productivity. Citeseer. https://doi.org/10.5251/abjna.2012.3.8.332.335
Peoples MB, Hauggaard-Nielsen H, Huguenin-Elie O et al (2019) The contributions of legumes to reducing the environmental risk of agricultural production. In Agroecosystem diversity (pp. 123-143). Academic Press. https://doi.org/10.1016/B978-0-12-811050-8.00008-X
Povero G, Mejia JF, di Tommaso D et al (2016) A systematic approach to discover and characterize natural plant biostimulants. Front Plant Sci 7:435. https://doi.org/10.3389/FPLS.2016.00435/FULL
Powers SE, Thavarajah D (2019) Checking agriculture’s pulse: field pea (Pisum Sativum L.), sustainability, and phosphorus use efficiency. Front Plant Sci 10, 1489. https://doi.org/10.3389/FPLS.2019.01489/FULL
Raffi M, Charyulu PB (2021) Azospirillum-biofertilizer for sustainable cereal crop production: current status. Recent developments in applied microbiology and biochemistry. Academic Press, pp 193–209
Ramya SS, Vijayanand N, Rathinavel S (2015) Foliar application of liquid biofertilizer of brown alga Stoechospermum marginatum on growth, biochemical and yield of Solanum melongena. Int J Recycl Org Waste Agric 4:167–173. https://doi.org/10.1007/S40093-015-0096-0/TABLES/4
Rani N, Kaur S, Nitu R et al (2020) Zinc solubilizing bacteria to augment soil fertility–a comprehensive review. Int J Agricult Sci Vet Med 8:38–44
Rani N, Kaur S, Kaur R, Chaturvedi S (2021) Microorganisms and carrier molecules used in biofertilizer formulations. J Pharma Res Int 33(60B):3952–3959. https://doi.org/10.9734/jpri/2021/v33i60B35099
Rastegari A, Yadav A, Yadav N (2020a) New and future developments in microbial biotechnology and bioengineering : trends of microbial biotechnology for sustainable agriculture and biomedicine systems: diversity and functional perspectives, 1st edn. Elsevier
Rastegari AA, Yadav AN, Yadav N (2020b) New and future developments in microbial biotechnology and bioengineering: trends of microbial biotechnology for sustainable agriculture and biomedicine. Elsevier
Raturi G, Sharma Y, Rana V et al (2021) Exploration of silicate solubilizing bacteria for sustainable agriculture and silicon biogeochemical cycle. Plant Physiol Biochem 166:827–838. https://doi.org/10.1016/J.PLAPHY.2021.06.039
Renuka N, Guldhe A, Prasanna R et al (2018) Microalgae as multi-functional options in modern agriculture: current trends, prospects and challenges. Biotechnol Adv 36:1255–1273. https://doi.org/10.1016/J.BIOTECHADV.2018.04.004
Romera FJ, García MJ, Lucena C et al (2019) Induced systemic resistance (ISR) and fe deficiency responses in dicot plants. Front Plant Sci 10:287. https://doi.org/10.3389/FPLS.2019.00287/FULL
Ronga D, Biazzi E, Parati K et al (2019) Microalgal biostimulants and biofertilisers in crop productions. Agronomy 9:192. https://doi.org/10.3390/AGRONOMY9040192
Saadaoui I, Sedky R, Rasheed R et al (2019) Assessment of the algae-based biofertilizer influence on date palm (Phoenix dactylifera L.) cultivation. J Appl Phycol 31:457–463. https://doi.org/10.1007/S10811-018-1539-6/FIGURES/3
Sabry AK (2015) Synthetic fertilizers; role and hazards. Fertil Technol 1:110–133. https://doi.org/10.13140/RG.2.1.2395.3366
Safinaz A, Ragaa A (2013) Effect of some red marine algae as biofertilizers on growth of maize (Zea mayz L.) plants. Int Food Researchj 20:1629–1632
Saharuddin, Dungga NE, Syam’Un E, Amin AR (2018) Towards sustainable agricultural production: growth and production of three varieties of shallot with some various Nitrobacter bio-fertilizer concentrations. Earth Environ Sci 157(1):012015
Salim B (2016) Influence of biochar and seaweed extract applications on growth, yield and mineral composition of wheat (Triticum aestivum L.) under sandy soil conditions. Ann Agric Sci 61:257–265. https://doi.org/10.1016/J.AOAS.2016.06.001
Sani I, Kurnia YW, Sinthya HC et al (2022) Exploring the potency of microalgae-based biofertilizer and its impact on oil palm seedlings growth. AGRIVITA J Agric Sci 44:139–151. https://doi.org/10.17503/AGRIVITA.V44I1.3102
Santana-Fernández A, Beovides-García Y, Simó-González JE et al (2021) Effect of a Pseudomonas fluorescens-based biofertilizer on sweet potato yield components. Asian J Appl Sci 9:2321–0893. https://doi.org/10.24203/AJAS.V9I2.6607
Selvam GG, Sivakumar K (2013) Effect of foliar spray from seaweed liquid fertilizer of Ulva reticulata (Forsk.) on Vigna mungo L. and their elemental composition using SEM–energy dispersive spectroscopic analysis. Asian Pac J Reprod 2:119–125. https://doi.org/10.1016/S2305-0500(13)60131-1
Shahwar D, Mushtaq Z, Mushtaq H et al (2023) Role of microbial inoculants as bio fertilizers for improving crop productivity: a review. Heliyon. https://doi.org/10.1016/j.heliyon.2023.e16134
Sharma SB, Sayyed RZ, Trivedi MH, Gobi TA (2013) Phosphate solubilizing microbes: sustainable approach for managing phosphorus deficiency in agricultural soils. SpringerPlus 2:1–14. https://doi.org/10.1186/2193-1801-2-587
Sheteiwy MS, Ali DFI, Xiong YC et al (2021) Physiological and biochemical responses of soybean plants inoculated with Arbuscular mycorrhizal fungi and Bradyrhizobium under drought stress. BMC plant biology 21(1):1–21. https://doi.org/10.1186/S12870-021-02949-Z
Singh M, Upadhyaya D, Bisht I (2013) Genetic and genomic resources of grain legume improvement. Newnes 1:305
Singh VK, Singh M, Singh SK et al (2019) Sustainable agricultural practices using beneficial fungi under changing climate scenario. In Climate change and agricultural ecosystems (pp. 25-42). https://doi.org/10.1016/B978-0-12-816483-9.00002-5
Singh H, Reddy SM (2012) Improvement of wheat and maize crops by inoculating Aspergillus spp. in alkaline soil fertilized with rock phosphate. Arch Agron Soil Sci 58:535–546. https://doi.org/10.1080/03650340.2010.532125
Stagnari F, Maggio A, Galieni A, Pisante M (2017) Multiple benefits of legumes for agriculture sustainability: an overview. Chemical and Biological Technologies in Agriculture 4(1):1–13. https://doi.org/10.1186/S40538-016-0085-1
Sunarpi H, Ansyarif F, Putri FE et al (2019) Effect of Indonesian macroalgae based solid and liquid fertilizers on the growth and yield of rice (Oryza sativa). Asian J Plant Sci 18:15–20. https://doi.org/10.3923/AJPS.2019.15.20
Suriya S, Boomibalagan P, Eswaran S et al (2018) Bio-fertilizer potential of seaweed liquid extracts of marine macro algae on growth and biochemical parameters of Ocimum sanctum. J Pharmacogn Phytochem 7:3528
Thakur M (2020) Fungi as a biological tool for sustainable agriculture. Agriculturally Important Fungi for Sustainable Agriculture: Volume 1. Perspective for Diversity and Crop Productivity, 255-273. https://doi.org/10.1007/978-3-030-45971-0_11
Thirumaran G, Arumugam M, Arumugam R, Anantharaman P (2009) Effect of seaweed liquid fertilizer on growth and pigment concentration of Abelmoschus esculentus (l) medikus. Am-Eurasian J Agron 2:57–66
Thornbro H (2022) 8 Plants commonly used to increase soil fertility-redemption permaculture. https://redemptionpermaculture.com/8-plants-commonly-used-to-increase-soil-fertility/. Accessed 28 Oct 2022
Tualar S (2013) Tropical bioresources to support biofertilizer industry and sustainable agriculture in Indonesia. In International Seminar on Tropical Bio-resources for Sustainable Bioindustry. pp 30–31
Tuhy Ł, Chowańska J, Chojnacka K (2013) Seaweed extracts as biostimulants of plant growth : review. Chemik 67(7):636–641
Wafaa A, Hendawy S, Hamed E, Toaima W (2017) Effect of planting dates, organic fertilization and foliar spray of algae extract on productivity of Dutch fennel plants under Sinai conditions. J Med Plants 5:327–334
White PJ, Brown PH (2010) Plant nutrition for sustainable development and global health. Ann Bot 105:1073–1080. https://doi.org/10.1093/AOB/MCQ085
Yamane K, Kono M, Fukunaga T et al (2014) Field evaluation of coffee grounds application for crop growth enhancement, weed control, and soil improvement. Plant Prod Sci 17:93–102. https://doi.org/10.1626/PPS.17.93
Yanebis Pérez Madruga IL-P (2020) (17) (PDF) Algae as a natural alternative for the production of different crops. Cultivos Tropicales 41(2)
Yulianingsih E, Pramono A, Setyanto P, Sugiarto (2021) Greenhouse gas emissions reduction and rice yield potential under bio-fertilizer application. In IOP Conference Series: Earth Environ Sci 648(1):012115
Zafar A, Ali I, Rahayu F (2022) Marine seaweeds (biofertilizer) significance in sustainable agricultural activities: a review. IOP Conf Ser Earth Environ Sci 974:012080. https://doi.org/10.1088/1755-1315/974/1/012080
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Ammar, E.E., Rady, H.A., Khattab, A.M. et al. A comprehensive overview of eco-friendly bio-fertilizers extracted from living organisms. Environ Sci Pollut Res 30, 113119–113137 (2023). https://doi.org/10.1007/s11356-023-30260-x
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DOI: https://doi.org/10.1007/s11356-023-30260-x