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Review

Fertilization and Soil Microbial Community: A Review

1
National Institute for Research and Development in Forestry “Marin Dracea”, 13 Closca, 500035 Brasov, Romania
2
Water Research Institute, National Research Council, Via Salaria km 29.300, Monterotondo Scalo, 00015 Rome, Italy
3
Faculty of Environmental Protection, University of Oradea, 26, Gen. Magheru Street, 410087 Oradea, Romania
*
Authors to whom correspondence should be addressed.
Appl. Sci. 2022, 12(3), 1198; https://doi.org/10.3390/app12031198
Submission received: 9 December 2021 / Revised: 18 January 2022 / Accepted: 20 January 2022 / Published: 24 January 2022
(This article belongs to the Section Environmental Sciences)

Abstract

:
The present paper reviews the most recent advances regarding the effects of chemical and organic fertilizers on soil microbial communities. Based on the results from the articles considered, some details are presented on how the use of various types of fertilizers affects the composition and activity of soil microbial communities. Soil microbes have different responses to fertilization based on differences in the total carbon (C), nitrogen (N) and phosphorus (P) contents in the soil, along with soil moisture and the presence of plant species. These articles show that the use of chemical fertilizers changes the abundance of microbial populations and stimulates their growth thanks to the nutrient supply added. Overall, however, the data revealed that chemical fertilizers have no significant influence on the richness and diversity of the bacteria and fungi. Instead, the abundance of individual bacterial or fungal species was sensitive to fertilization and was mainly attributed to the changes in the soil chemical properties induced by chemical or organic fertilization. Among the negative effects of chemical fertilization, the decrease in enzymatic activity has been highlighted by several papers, especially in soils that have received the largest amounts of fertilizers together with losses in organic matter.

Graphical Abstract

1. Introduction

Crop production is currently expanding globally due to an increased demand for food, animal feed and biofuels; the latter has been stimulated by the increase in oil prices making bioenergy crops more competitive and profitable compared to fossil fuels [1]. Currently, 47.9 million km2 are devoted to agriculture, which is about 50% of habitable land [2].
Higher yields and better harvest quality can be achieved through the optimized use of fertilizers and the implementation of strategic production practices. Chemical fertilizers (also termed mineral, inorganic or synthetic fertilizers) contain a high concentration of a primary nutrient (nitrogen, N; potassium, K; phosphorous, P) as inorganic salts. Secondary elements (calcium, magnesium and sulfur) can also be added to soil by chemical fertilizers. Micronutrients (boron, manganese, iron, zinc, copper, molybdenum, cobalt and chlorine) [3] are in general absent in NPK chemical fertilizers and can be supplied by specific synthetic and expensive plant nutrients with soil or foliar applications [4].
The nutrient content in chemical fertilizers is indicated as the N:P:K rate, representing the percentages of nitrogen, total phosphorus (in the form of phosphorus pentoxide, P2O5) or total K (in the form of potassium oxide, K2O). If they also contain secondary elements, numbers in brackets specify calcium oxide (CaO), magnesium oxide (MgO), sodium oxide (Na2O) or sulfur trioxide (SO3) content.
The majority of the inorganic fertilizers (with the exception of N) is extracted from rocks using physical or chemical processes. N fertilizers (mainly as ammonium—NH4+—and nitrate—NO3: urea, urea ammonium nitrate, ammonium nitrate and calcium ammonium nitrate) are produced by combining atmospheric N2 with hydrogen (mainly from hydrocarbons such as natural gas—CH4) to obtain anhydrous ammonia (NH3), which can be used directly as a plant nutrient or converted into other different N fertilizers [5,6]. Phosphate fertilizers (principally single superphosphate, triple superphosphate, mono-ammonium phosphate, di-ammonium phosphate and ammonium polyphosphate liquid) are extracted from natural phosphate rock deposits [7]. K fertilizers (potash muriate, KCl; potassium sulfate, K2SO4; potassium nitrate, KNO3; sulfate potash magnesia, K2SO4·MgSO4; kainite, KCl + NaCl + MgSO4) are produced by different chemical processes [8].
Differently, organic fertilizers (Table 1) are derived from plant- or animal-based materials or other organic constituents that are either a by- or end-product of naturally occurring processes, containing both the essential nutrients and micronutrients for plant growth. They also comprise biofertilizers (bacteria, algae, fungi or biological compounds), including plant-growth promoting bacteria [9,10,11].
Inorganic and organic fertilizers have an important role in increasing agricultural production, but the use of mineral fertilizers is constantly growing, with an estimated total 186.67 million tons in 2016 [12]. There is increasing concern regarding the negative environmental effects of chemical fertilizers. In fact, they can cause serious greenhouse gas (GHG) emissions and pollution of soil and water ecosystems. For example, synthetic nitrogen fertilizers have been recognized to be the most important factor contributing to direct N2O emissions into the atmosphere as a consequence of their biodegradation by soil microorganisms [13]. In addition, only 50–60% of synthetic nitrogen fertilizers added to soil is usually taken up by crops [8], and the rest runs off into water bodies (surface or groundwater [14]) due to their high dissolution properties. A possible alternative is the use of controlled-release fertilizers (coated and uncoated fertilizers with a low solubility) [15], but they are expensive and, therefore, used mainly for high-value crops (e.g., vegetables, fruits, flowers, ornamentals) [8]. Inhibitors of nitrification and urease processes can also be used for maintaining N in its soil-stable form by slowing its conversion to nitrate or delaying the first step of degradation of urea [16]. For these compounds (such as dicyandiamide, thiosulfates, 3,4-dimethylpyrazole phosphate), there is a lack of correlation between laboratory testing data and the actual field data [17]; there is also some concern about the potential for some of them to enter the food chain [18].
Phosphorus availability to plants after chemical fertilization can vary depending on the type of fertilizer used and, even under the best conditions, only about 25% of applied P is taken up by plants during the first cropping season [19]. Depending on the pH and moisture of soil, P can than precipitate (at high pH due to the presence of calcium and magnesium and at low pH due to an iron and aluminum presence) [20] or can be immobilized in soil [21]. The use of P fertilizers also leads to eutrophication (when P runs off to surface waters) [22]. Potassium has several beneficial roles in plant physiological and metabolic processes, including resistance to biotic and abiotic stresses and absorption and utilization of N and P by crops [23]. On the other hand, fertilization with KCl does not increase crop yields and has detrimental effects on the quality of major food, feed and fiber crops, with serious repercussions for soil ecosystem and human health [24].
Conversely, organic farming using organic fertilizers that are environmentally friendly amendments (e.g., microbial fertilizers [25,26], manure, compost) can be a good alternative and can reduce the consequences of environmental pollution from synthetic fertilization. In fact, organic fertilizers for example gradually release primary and micronutrients into the soil, maintaining a nutrient balance for a healthy growth of crop plants. They can also be an effective source of soil microbes, while also improving soil structure [27]. Table 1 shows a list of the main organic fertilizers.
Fertilizers and amending materials are regulated in the EU by the Regulation 2019/1009. In the US, they are differently regulated at the state level rather than by the federal government.
Fertilizers in China are controlled by several regulations and standards. Importing, producing, selling or utilizing un-registered fertilizers is not allowed. Moreover, fertilizers sold in China also have to meet important product standards and requirements for their marking, with the compulsory national standard GB 18382-2021, which was issued in 2021 and comes into force on 1 May 2022. The “Mandatory national standard GB 38400-2019 Limit requirements for toxic and harmful substances in fertilizers” that comes into force on 1 July 2020, defines the hazardous substance limits in fertilizers (i.e., heavy metals).
In Brazil, the main regulatory agencies for fertilizers are MAPA (the Brazilian Ministry of Agriculture, Livestock and Food Supply), ANVISA (Brazilian Health Regulatory Agency), MMA (Brazilian Ministry of Environment) and INMETRO (Brazilian National Institute of Metrology, Quality and Technology). Law 6894/80, also called the “Fertilizer Act”, contains the general rules regarding the registration and classification of such products. It is devoted to the inspection of the production and trade of fertilizers (including also correctives, inoculants, stimulants, bio-fertilizers, remineralizers and substrates for plants). All these fertilizers have to be registered at the Ministry of Agriculture. The Fertilizer Act is regulated by the Decrees n. 4954/2004 and n. 8384/2014.
In India, the Ministry of Chemicals and Fertilizers (https://fert.nic.in (accessed on 18 January 2022)) is devoted to the regulation of fertilizers. The Fertilizer Control Order provides for registration of fertilizer manufacturers, importers and dealers; it is specifically for all fertilizers manufactured/imported and sold in the country, regulating also fertilizer mixtures, and the packing and brand description on the fertilizer bags etc. Chemical fertilizer consumption has been generally increasing in India during the last 4 years, with a maximum of 59.88 million tons of fertilizer products used (mainly urea, di-ammonium phosphate, murate of potash, complexes and single super phosphate), as recently reported by the Indian Ministry of Agriculture and Farmers’ Welfare (https://pib.gov.in/PressReleseDetail.aspx?PRID=1696465 (accessed on 18 January 2022)).
Soil biota encompasses a huge diversity of organisms, including microorganisms (i.e., bacteria, fungi and archaea), which are the largest group of soil organisms in terms of number and biomass [52]. Soil microbial communities play important roles in ecosystem functions and regulate key processes, such as the carbon and nitrogen cycles [53]; for example, microorganisms carry out the ecological functioning of N2-fixation, ammonia-oxidation, denitrification and ammonification. Microbial communities are also key players in the degradation of various compounds, including organic pollutants such as pesticides [54], and they promote plant growth and disease control [55]. The diversity and biomass of soil microbial communities are the major regulators of fundamental ecosystem processes [55], supporting crop production [52]. In fact, a good soil quality, which means a diverse and abundant microbial community and activity, is a pre-requisite for plant growth and, consequently, for crop production [56]. In particular, soil microbial biomass, activity and diversity are an indicator of soil fertility and ecosystem productivity [57,58]. For this reason, they are used as indicators of soil quality and health [52,59]. Soil quality is defined as the capacity of a specific kind of soil to function, within natural or managed ecosystem boundaries, to sustain plant and animal productivity, maintaining or enhancing water and air quality, and supporting human health and habitation [60]. Microbial populations vary depending on different abiotic factors such as soil type, presence/absence of plants and climate; their responses to similar fertilization treatments can thus be different depending on the above-mentioned abiotic factors. During the long-term process of evolution, soil, plants and microbes co-evolved to form relatively stable relationships within a given ecosystem. In fact, the soil microbial community has recently been termed the soil microbiome [53,61,62]. Changes in soil microbial communities induced by environmental changes could influence the relationships between microorganisms and plants and may negatively influence soil fertility and crop productivity. Consequently, studying the effects of chemical/organic fertilizers on the natural microbial community is of crucial importance. For example, understanding how NPK chemical fertilizers influence the microbial biomass, which is an indicator of soil fertility and quality, is a basic prerequisite for understanding microbiological processes [63], in order to preserve the ecosystem functions of soil.
These research themes are an important part of soil ecology, as pointed out by several international authorities (e.g., EU commission, FAO [64,65]). The use of inappropriate farming practices (e.g., excessive use of chemical fertilizers and pesticides) and frequent changes in land use may cause variability in soil microbial communities, which can have significant effects on soil fertility and productivity [66].
The present article reviews the importance of soil microbes for the soil ecosystem, with a particular emphasis on the influence of chemical and organic fertilizers on the soil microbial community. In particular, microbial biomass, activity and diversity were taken into account as parameters. For microbial activity, dehydrogenase activity, a general indicator of microbiological activity [67,68] is considered.

2. Materials and Methods

This review considers articles published between 1990 and 2022 regarding the effects on soil microorganisms of chemical fertilization in long-term field experiments, in particular with reference to control soils (not fertilized) or soil fertilized with organic amendments. The articles were both original studies and literature reviews, scoping reviews and systematic reviews with state-of-the-art knowledge of the topic [69].
The criteria used in this review for searching articles were:
-
Type of publications (only original studies or reviews were considered);
-
The main direction of the systematic review consisted in reviewing the fertilizer types and fertilizer treatments used in different countries of the world;
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Effects of chemical fertilizer management on soil microorganisms in agroecosystems across the world, also compared with organic fertilization;
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Influence of intensive and/or long fertilization on the numbers and activities of microbial communities in soils;
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Comparison between the various fertilizer regimes and their effects on soil microorganisms.
Exclusion criteria consisted in:
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Editorials;
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Studies published in a language other than English;
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Studies in specific extreme areas (e.g., arctic or arid soils).
To find the main relevant studies, ERIC (Education Resources Information Center) was used together with numerous databases, including Web of Science, Science Direct, SpringerLink and Google Scholar. The primary keywords used in the different databases were: “use of chemical fertilizers”, “influence of phosphorus on soil bacteria”, “fertilizers and soil microorganisms”, “soil bacteria affected by fertilizers”, “long-term fertilization effects on soil microorganisms”, “ecological consequences of the fertilizers” and “combined fertilization”.
In Figure 1 a sketch containing the methodology steps used is presented.

3. Results and Discussion

Overall, a total of 52 articles were considered (Table 2). A significant proportion of the papers on the effects of inorganic or organic fertilizers on soil microbial communities were published by Asian authors (Chinese), representing about 28% of the total. Other important studies have been performed by European and North American authors, with numerous works being dedicated to this subject during recent years. Because the effects of fertilizers were not influenced by Country, the main considerations in the following paragraphs were grouped in categories such as effects of chemical fertilizers (NPK) on soil microorganisms/soil microbiome, types of fertilizers used and their influence, species of bacteria affected by fertilizers and the negative effects of fertilizers on soil microorganisms (Table 2).

3.1. Effects of Chemical Fertilizers on Biomass, Activity and Diversity of Soil Microorganisms

It has been generally shown that both chemical and organic fertilizers can directly stimulate the growth of specific microbial populations by supplying nutrients [70], leading to an increase in total microbial numbers [71,72,73,74], improving microbial activity [75] and determining a switch in microbial diversity. A high soil microbial diversity is crucial for the productivity and stability of the agroecosystems [76]. In several studies, mineral fertilization has been found to reduce microbial diversity, including the plant-beneficial microbial taxa [76]. Meta-analysis of microbial communities, based on 107 datasets from 64 long-term trials from around the world, concluded that mineral fertilizer application (in particular N fertilizer treatment) leads to a 15.1% increase in microbial biomass compared to unfertilized control plots; moreover, N application (urea and ammonia fertilizers) can have a temporary or stable effect in increasing pH [77,78,79]. However, the use of a chemical fertilizer alone does not lead to a remarkable increase in soil microbial abundance. This was observed in a rice–wheat cropping system [80], in a drip-irrigated cotton systems [74] and in paddy field soils [81]. Long-term mineral fertilization, and in particular N addition, increases microbial biomass beca.use soil microorganisms may be carbon- or N-limited. The increase is significant if soil pH is >5; in other cases, fertilization reduce microbial biomass [77].
Soil-available P and total N are the most important factors influencing the abundance of microbial communities involved in the nitrogen cycle [82]. However, chemical fertilization, in particular N addition, was found to decrease bacterial alpha-diversity [83], although a recent study found that soil fertility and plant yield was mainly due to bacterial and archaeal abundance and community structure rather than bacterial, archaeal or fungal alpha-diversities [84]. In fact, the increase in microbial biomass has been attributed to better plant growth, which results in higher rhizodeposition [85]. The latter was found to be more active in determining a shift in the fungal community [86]. That is, soil bacteria were more sensitive than fungi to fertilization practices [87,88]. In addition, the plant composition and carbon substrate utilization patterns of rhizobacterial communities were more diversified in unfertilized plots than in chemical fertilized plots in grasslands [89]. Long-term NPK applications have been found to result in a loss in soil organic matter (SOM), especially in arid and semi-arid areas or where a monoculture is performed (e.g., corn) [90,91,92]. An increase in SOM by mineral fertilizers has been found only when they are applied in combination with organic amendments [93,94]. SOM quality greatly influences soil microbial community composition [95]. Soil quality and crop yield also depend on SOM content [4]. The latter affects the availability of micronutrients, with higher micronutrient amounts in higher SOM content [4]. Moreover, SOM quality (e.g., organic acid, protein, humic acid and lignin content) and its biodegradability essentially influence microbial characteristics (e.g., specific population size, microbial activity and composition) [94,96]. Consequently, any SOM depletion has negative consequences for microbial community richness together with lower plant health, growth and productivity.
In general, organic fertilizers improve soil structure (in terms of particle-size fraction [97]), and they are responsible for a more balanced and stable nutrient supply, which can sustain a more diverse microbial community if compared to mineral fertilizers [98]. Moreover, organic fertilization is reported to increase microbial activity and SOM content and improve the chemical and physical properties of soil better than inorganic fertilization [99,100,101], preventing the decrease in soil pH due to mineral fertilizer application [90]. In any case, long-term inorganic or organic fertilization significantly decreased soil pH if compared to a non-fertilized control [86], although soil pH changes due to organic amendments depend on the amendment used [102]. For example, some biochar was found to increase soil pH [102], whereas manure could in general decrease soil pH [103].
Dehydrogenases are respiratory enzymes that oxidase organic compounds allocating two hydrogen atoms from these compounds to electron acceptors, producing energy [58]. These enzymes are present in all soil microorganisms and are not present as a free form, representing only the activity of live microbial cells. Consequently, dehydrogenase activity has been considered as an indicator of soil microbiological activity [58,67,68,104].
Dehydrogenase activity (DHA) was found to be lower in soils that had received high (160 N, 120 P2O5, 160 K2O) amounts of NPK fertilization [98], suggesting that these enzymes are highly sensitive to the inhibitory effects associated with high mineral fertilization. In addition, long-term P-deficiency fertilization can significantly decrease DHA together with soil microbial biomass and bacterial diversity [90]. Although an NPK balanced fertilization can increase DHA, the higher increase is always found with organic fertilization [71]. Applying phosphorus-based fertilizers has been shown to lead to seasonal variations in microbial activity, as well as in the abundance of specific bacterial and fungal phospholipid fatty acid (PLFA) indicators of soil microbial biomass [105,106,107].
In their experimental study, Enebe and Babalola [108] examined the response of maize bacterial, fungi and archaeal communities to compost and inorganic fertilizations. The results showed that both fertilizers influenced the maize rhizosphere microbial community but the organic amendments provided the most stable microbial community; these results were also found by Zhang et al. [109], in which higher levels of NPK treatments (60 kg of NPK fertilizer as N/ha) negatively affected the microbial community structure and abundance in an agricultural soil.
On the other hand, long-term fertilization with organic amendments can both mitigate the negative effects and exploit the positive effects of climate change on crop production, enhancing soil quality and improving crop productivity, as was observed by several authors (e.g., Song et al. [110] in northeast China).
In an overall view, although it is not possible to summarize all the beneficial effects of organic fertilizers because they are very different in type of production, content in essential nutrients (NPK), pH, structure, etc., they always improve soil structure and organic matter content of soil, together with an increase in microbial communities. Moreover, thanks to the soil quality improvement, they also favor microbial community abundance and activity. On the other hand, although mineral fertilizers, apart from their environmental side effects (GHG emission, soil and water pollution), provide essential nutrients, long-term application contributes to soil depletion. In fact, soil treated only with chemical fertilizers relies solely on the root residues and exudates of the crops to increase carbon input [93].

3.2. Types of Fertilizers Used and Their Influence on Soil Microbial Community

The sustainable development of agroecosystems is based on a better understanding of the complex responses of microbial communities to the various organic and inorganic fertilization regimes, as highlighted by Pan et al. [111], demonstrating that a better understanding of the complex responses of microbial communities to various organic and inorganic fertilizations is critical for a sustainable development of agroecosystems. They found that using chemical fertilizer together with manure clearly increased soil fertility and were recommended for further optimization of fertilization patterns. In addition, the results of their research suggested that organic and inorganic fertilizers dominated in shaping bacterial and fungal community distributions in fluvo-aquic soils.
Nakhro and Dkhar [81] compared the use of organic fertilizers with inorganic ones, observing that organically treated soils had the largest number of microorganisms (fungi and bacteria) and microbial biomass carbon. Chemical fertilizers, on the other hand, have been shown to have a smaller effect than other soil treatments on bacterial composition and diversity [112].
Comparing the effects of chemical fertilizers with manures (farmyard manure, slurry and green manure), Edmeades [113] concluded that there is no significant difference in the long-term effects on crop production between these two types of fertilization. However, manured soils had higher organic matter contents and higher numbers of microfauna than soils added with chemical fertilizers. The manured soils were also more enriched in P, K, Ca and Mg in the topsoil and nitrate, N, Ca and Mg in the subsoil.
When an organic fertilizer is applied to soil, its decomposition is due to bacteria and fungi, which in turn support the soil fauna chain. The ratio of fungal to bacterial biomass can be considered an indicator of the activity of two pathways of the soil food web, formed by fungivores or bacterivores and their predators, respectively [114]. In general, bacteria are prevalent under conventional tillage, whereas fungi dominate under no-tillage. The use of nitrogen fertilizers by applying organic amendments decreases the fungi/bacteria ratio and can decrease the soil pH [114]. For this reason, several countries encourage farmers in economically developed areas to reduce their N fertilization rate [115]. Cruz et al. [116] concluded that mineral fertilization, which modifies available N and P and hence changes in soil fertility, can be a selective force causing structural and functional shifts in the soil microbial community. Furthermore, a mixed application of N, P and K has been shown to increase soil microbial biomass and diversify bacterial communities [117]. In several studies nitrogen addition is a key factor in bacterial and fungal community composition shifts [87].

3.3. Bacterial and Fungal Species Affected by Chemical or Organic Fertilizers

Several authors have demonstrated that the structure of the soil microbial community (composition, diversity, and relative abundance of specific taxa) changes after chemical or organic fertilization [25,80,118,119,120]. In fact, the latter affects microbial growth and competitiveness because different bacterial and microfungal groups can vary in their ability to use the different nutrient forms found in soil [76,90,121]. For example, Knufia petricola and Zygomycetes fungi were found only in the inorganic fertilization of soil. K. perticola is a microcolonial Ascomycete adapted to extreme environments, and Zygomycetes are typical r-strategists with a rapid growth with simple carbon sources [122]. Moreover, some typical bacteria from organic amendments (e.g., Firmicutes and Myxococcales) were found as primary constituents in manured-traded soils [121,123]. Specific microbial groups (Firmicutes, Proteobacteria, and Zygomycota) are stimulated to grow in organic fertilizer treatments, because they prefer nutrient-rich environments, and are capable of degrading complex organic compounds [76].
Many studies have focused on the impact of different types and regimes of fertilization on the soil microbial communities, and the results are in some case conflicting for chemical fertilizers. For example, Sun et al. [82] focused on the effects of long-term fertilization with NPK or NPK + organic amendments on specific bacterial and archaeal genes involved in the nitrogen cycle. They suggested that the genes for ammonia-oxidization are more sensitive than nitrogen fixers and denitrifiers to fertilization. Although they found that NPK increased soil fertility in terms of genes involved in the nitrogen cycle, the organic amendments induced greater gene abundance. Interestingly, soil available P was the most important factor influencing the abundance of functional communities involved in the nitrogen cycle.
Long-term agricultural organic and chemical fertilization significantly affects nitrogen cycling in soils [97,98,124,125,126]. For example, in calcareous soils, N fertilization increases the potential nitrification rate but reduces the efficiency use of N and changes the beta-diversity of ammonia-oxidizing bacteria (AOB), reducing the relative abundance of Nitrosospira (nitrite-oxidizing bacteria) and increasing the relative abundance of Nitrosomonas (which oxidize ammonia to nitrite) [126]. On the other hand, mineral and organic fertilizer application significantly increased the species richness and alpha-diversity of AOB [125]. In contrast, Wang et al. [78] revealed that the long-term application of manure and chemical fertilizers significantly affected microbial community structure, and specifically, NPK significantly reduced the alpha-diversity of the soil microbial community.
The influence of fertilization on the r to K member ratio has been reported in some papers. In general, r-strategists grow fast when the substrate is abundant, and include copiotrophic bacterial taxa such as Proteobacteria and in particular Alpha- and Beta-Proteobacteria, Firmicutes, Actinobacteria and Candidatus Saccharibacteria. K-strategists can grow when resources are limited and include oligotrophic bacteria such as Acidobacteria, Gamma- and Delta-Proteobacteria, Gemmatimonadetes, Verrucomicrobia and Chloroflexi [76,127,128].
The application of chemical fertilizers has been reported to enrich the K-strategist bacterial community [76,93,129,130]. It was for example found in a silt loam soil in a long-term experiment with wheat (Triticum aestivum L.) plantation. Wang et al. [131] in meadow grassland soils reported that N and P fertilizations shifted soil microbes towards an r-selected community. Nutrient addition (both organic and chemical) have been found to enrich copiotrophic taxa affiliated with the Pseudomonadaceae and Cytophagaceae bacterial families but to reduce some Acidobacteria [86]. In particular, Cyanobacteria (an active N-fixing group) increased in soils amended with inorganic fertilizers. Manure application, on the other hand, increased the relative abundance of the Gamma-Proteobacteria group (responsible for organic substrate decomposition) and Nitrosomonadaceae (Beta-Proteobacteria), which play a vital role in converting ammonium into nitrate [86].
Overall, organic and inorganic fertilizers generally have positive effects on numerous soil bacteria, the most representative of which is Azotobacter. The latter is in fact a free-living, nitrogen fixing aerobic soil bacterium able to make available to plants a considerable part of soil nitrogen [132]. For example, the mineral fertilization of an apple (Malus domestica) orchard after replanting caused increased number of Actinomycetes, Azotobacter, proteolytic bacteria and phosphate-solubilizing bacteria [133]. Likewise, the use of inorganic fertilizers on a semi-arid alfisol led to an increase in the numbers of Azotobacter, even though the genetic diversity was unaffected [134]. Similar results were obtained in maize cultures [135] and in sugarcane cultures [136].
Chemical N addition was found to increase the relative abundance of oligotrophic bacteria and can have positive effects on some bacterial groups involved in C cycling such as Ktedonobacteria and Acidobacteria in extremely acidic subtropical forests [83].
On the other hand, intensive mineral N fertilization can negatively affect other specific bacterial groups (e.g., Diazotrophs, Beta-Proteobacteria) that are important rhizosphere microbes with symbiotic N-fixing interactions with leguminous plants.
The first step in nitrification (oxidation of ammonia into nitrite) is performed in soil by ammonia-oxidizing archaea (AOA) and AOB (Beta- and Gamma-Proteobacteria) [137]. AOA, which are 2- to 3000-fold more abundant than AOB in soils [137] and are key players in the N cycle in unfavorable environmental conditions (e.g., low nutrient content, low pH) [138], are more sensitive than AOB to different chemical fertilization treatments in acidic red paddy soil [138]. In this study, the AOA structure was more negatively affected. The long-term application of chemical NPK or N fertilizer has been found to significantly affect soil microbial communities throughout the soil profile and increase the relative abundance of AOA in surface soil (0–40 cm) only in the presence of additional organic fertilization (recycled crop residues or manure) [79,138]. This implies that the important ecological function of soil nitrification can be promoted only with simultaneous chemical and organic fertilization.
Phylogenetic analyses performed in a long-term organic and chemical fertilization experiment in a sandy loam soil in northern China indicated that Proteobacteria was the dominant taxonomic group in the soil, followed by Acidobacteria and Gemmatimonadetes [139]. In this study, long-term PK treatment was found to enhance bacterial richness and diversity more than NK, NP, NPK or organic manure addition. Da Silva and Nahas [140] found that the number of spore-forming Gram-positive rods was higher in plots with superphosphate.
Specific bacterial groups are enriched by organic fertilization, such as Alpha-Proteobacteria, Gamma-Proteobacteria, Nitrospirae, Bacterioidetes and Actinobacteria [141]. This was also found by Liang et al. [142], who studied the effects of different fertilization treatments (no fertilizer added, nitrogen fertilizer and bioorganic fertilizer) on the rhizosphere bacterial community. They found that the soil rhizosphere of winter wheat treated with bioorganic fertilizer had a higher microbial diversity than other treatments. The relative abundance of Proteobacteria in soil treated with bioorganic fertilizer was significantly higher than without fertilization, while Acidobacteria were significantly lower.
Summarizing the studies reported here, organic fertilizers increase soil organic matter and micronutrient contents, improve soil structure and promote a higher microbial diversity. Moreover, adding organic matter also favors the microbial activity that can be measured by dehydrogenase activity, related to soil quality. Finally, although depending on soil type, specific groups linked to fundamental nutrient cycling such as Proteobacteria Firmicutes are promoted by organic fertilization, probably because of both organic carbon improvement and the addition of specific microbial groups from the organic fertilizers.
In contrast, long-term N input by chemical fertilization not only decreases soil pH but also diminishes the relative abundances in particular microbial groups possessing genes related to P-solubilization. Moreover, the abundances in Proteobacteria such as Alpha-Proteobacteria and Gamma-Proteobacteria, together with some Actinobacteria containing genes coding for mineralize organic-P compounds in soils (e.g., alkaline phosphatase), are disadvantaged. Microbial groups related to nitrogen cycle (AOA and AOB) could be favored only with a combined chemical and organic fertilization.

3.4. Negative Effects of Chemical Fertilizers on Soil Ecosystem

The application of chemical fertilizers alone generally improves crop production; however, concerns have been raised not only about the severe environmental problems posed by such practices but also about the long-term sustainability of such systems [143]. It was also highlighted that synthetic fertilizers can increase disease incidence [144,145]. In some cases, the availability of some micronutrients (e.g., zinc) is reduced below the critical value, probably due to zinc precipitation by high concentrations of available soil P [146]. Long-term mineral fertilizer applications result in a significant loss in SOM, as found in monocultures performed for long periods without any addition of organic fertilizers and without crop rotation [90,91,92,147]. Mineral fertilization has also been found to cause decreases in porosity and nutrient availability of soil [110]. Moreover, mineral fertilization strongly affects the number of microorganisms and the qualitative selection of entire communities of soil microorganisms [59]. The study by Birkhofer et al. [148] indicates that the use of synthetic fertilizers and herbicides changes interactions within and between below- and above-ground components of the soil microbial community and ultimately increases the negative environmental impacts of agriculture by reducing internal biological cycles and pest control.
The long-term use of mineral fertilizers may be harmful, particularly at high rates of nitrogen fertilization, as it leads to increased gaseous nitrogen losses and to the deterioration of physical, chemical and biological soil properties [149,150]. Other studies (e.g., Doran et al. [59]) indicate that agricultural chemicalization, especially in the form of high rates of N fertilizer application on arable, grassland and horticultural soils, might not only risk the biological productivity and ecological stability of agroecosystems but also threaten surface and groundwater through the accumulation of nitrates, nitrites and many other organic nitrogen compounds [151].
Elevated concentrations of soil P have also been implicated in the P enrichment of shallow groundwater feeding coastal, lake and river ecosystems [152,153].
Fungi and their enzymes are less sensitive to the action of chemical fertilizers [154]. In particular, in the study by Marschner [155], only protease activity was affected by fertilization in the case of the enzymes studied.
Dangi et al. [156] suggested that the use of organic fertilizer or organic amendments can potentially mitigate the deleterious environmental impacts of inorganic fertilizers in agroecosystems, but they can also affect soil microorganisms that have not been well defined. They found that soil amendment such as biochar or the incorporation of other organic fertilizer for about two years affected microbial community biomass, composition and crop yield.
A possible combination of chemical and organic fertilization was found to be a good way to not only improve soil fertility, but also for enhancing crop yield, in particular for soils with low N, P and organic carbon content [157].

4. Some Consideration for Organic Amendments Used as Fertilizer

Organic amendments are defined as any materials originating from plants or animals and used for improving soil physical, chemical and biological properties, making a better soil quality for supporting plant productivity [8]. In fact, adding large nutrient quantities and exogenous microbes to soil can interfere with the indigenous bacteria growth, promoting the colonization of fertilizer-derived bacteria [158].
Long-term application of organic amendments in general improves soil fertility and soil structure, promoting the development of a beneficial soil microbiota capable of supporting high plant yield under intensive agricultural systems [159].
The most common soil organic amendments (Table 1) are animal manure [160,161,162,163], municipal biosolids [33], crop residues (forage or various crop varieties), compost and digestate. Some complementary fertilization options other than the use of chemical fertilizers include the use of bio-surfactants [164], biomineralization [165] and biofertilizers [166,167,168], including microbial suspension and seaweed concentrate [25,169,170]. The use of plant growth-promoting microorganisms [171] is a very promising tool that could also have positive effects by inhibiting pathogens through the production of antibiotics or cell wall lytic enzymes, inducing plant defence mechanisms [172].
Compost is derived from green waste or from sewage sludge [173]. Digestate can be derived from anaerobic digestion of several organic residues or organic wastes, including manure from farms, energy crops, municipal sewage sludge, biosolids and agro/food industry by-products [173].
Some organic amendments (manure, compost, digestate) could have some environmental side effects. For example, manure application can increase the abundance in soil of antibiotic resistance genes (soil antibiotic resistome) if the animals are treated with antibiotics for prophylaxis or therapeutic treatments [78]. Composting and anaerobic digestion has been suggested as a potential strategy to eliminate or diminish antibiotic residues and pathogens in livestock manure before its application as an organic fertilizer in agro-ecosystems [42,43,174].
Compost and digestate could also contain other contaminants in residual concentrations, such as heavy metals (e.g., nickel, lead, copper, zinc, mercury), although there are currently legislative limits for several compounds for the application of these organic amendments in agroecosystems [39].

5. Conclusions

Soil is of critical importance thanks to its role in several ecosystem functions, including food production. The soil microbial community has a crucial role in these functions. It also has a key role in the availability and accessibility of nutrients to plants and exerts plant bioprotection. Soil biochemical, microbiological and biological properties have been used for several years for estimating alterations in soil quality. However, the effects on soil microbial community and consequences on soil fertility have not been adequately studied at different levels. At the EU level, there is not currently a regulation regarding soil, and it is advisable that the microbial community should be considered and preserved.
Chemical fertilizers are sources of NPK nutrients in their inorganic forms and do not exert beneficial effects on soil physical properties (e.g., texture, structure, porosity, etc.) and SOM content. Absence of or leftover or incorrect addition of N, P and K fertilizers can affect the absorption and use of nutrients (including micronutrients), and because it negatively affects the beneficial plant rhizobacteria, it reduces crop yield and quality. Organic and synthetic fertilizers can affect microbial community compositions, favoring species functionally adapted to the nutrient inputs and activity and, ultimately, enhancing plant productivity. It is well known that chemical fertilizers can cause different environmental problems, including biodiversity loss, as highlighted by the new EU Soil Strategy for 2030, loss of SOM, deterioration of physical and chemical soil properties and, especially with long-term application, the lowering of soil fertility. Sustainable agriculture that limits chemical fertilization but also favors crop rotation, reduced soil tillage and extensified land use is an important global issue for preserving natural microbial communities (in terms of species abundance and richness of specific beneficial microorganism groups in soil), maintaining their ecological function and sustaining soil fertility.
Because it is not reasonable to use only organic amendments to support plant productivity since they do not provide high amounts of NPK, a combined addition of chemical and organic fertilizers could be the right solution, particularly for soils with low N, P and organic C contents. In particular, the so-called 4 Rs for nutrient management, i.e., “right source, right rate, right time and right place” could be the correct path for farmers to manage fertilization of soil. Considering that, each basic element (N, P, K) has to be applied with a balanced fertilization by organic (including bio-organic) and synthetic fertilizers considering the soil needs; the role of micronutrients is also fundamental (for example in stimulating the availability of P). In any case, because the fertilization strategy is frequently related to economic rather than agronomic evaluations, N and, to a lesser extent, P are the only nutrients used and K fertilization is underexploited, so there is still a widespread unbalanced fertilization. A combined fertilization with chemical and organic fertilizers (in particular with compost, digestate or plant residues) could be a good compromise for providing basic elements together with micronutrients and improving soil organic carbon and increasing several physico-chemical soil properties. The new era in the use of plant-growth-promoting microorganisms can lead to a decrease in use of chemical fertilizers, although this practice still needs to better investigated and adapted to specific soils and plant cultivations. Finally, it has to be taken into account that the EU Fertilizing Products Regulation (Reg. 2019/1009 EU), which governs the production and addition to agroecosystems of organic and inorganic fertilizers, organo-mineral fertilizers, soil improvers, liming materials, plant biostimulants, inhibitors, and fertilizer products, will be implemented in 2022, and the fertilizing product quality certification process will be harmonized across the EU.
Any improvement in plant quality (e.g., genetically engineered crops able to form nitrogen-fixing symbioses and fixing nitrogen without microbial symbionts) avoiding or reducing the use of mineral fertilization also has to be promoted.

Author Contributions

Conceptualization, L.C.D., P.G. and A.O.; methodology, C.O. and A.O.; investigation, L.C.D., C.O. and A.O.; writing—original draft preparation, P.G.; writing—review and editing, P.G., L.C.D. and A.O. All authors have read and agreed to the published version of the manuscript.

Funding

This research received no external funding.

Institutional Review Board Statement

Not applicable.

Informed Consent Statement

Not applicable.

Data Availability Statement

Not applicable.

Conflicts of Interest

The authors declare no conflict of interest.

References

  1. Winkler, K.; Fuchs, R.; Rounsevell, M.; Herold, M. Global land use changes are four times greater than previously estimated. Nat. Commun. 2021, 12, 2501. [Google Scholar] [CrossRef] [PubMed]
  2. FAO. The World Bank Data, Food and Agriculture Organization. 2018. Available online: https://data.worldbank.org/indicator/AG.LND.AGRI.K2 (accessed on 10 November 2021).
  3. ISO. ISO 8157:2015, Fertilizers and Soil Conditioners; ISO: Geneva, Switzerland, 2015; Available online: https://www.iso.org/standard/59567.html (accessed on 10 November 2021).
  4. Thapa, S.; Bhandari, A.; Ghimire, R.; Xue, Q.; Kidwaro, F.; Ghatrehsamani, S.; Maharjan, B.; Goodwin, M. Managing Micronutrients for Improving Soil Fertility, Health, and Soybean Yield. Sustainability 2021, 13, 11766. [Google Scholar] [CrossRef]
  5. Zhang, W.-F.; Dou, Z.-X.; He, P.; Ju, X.-T.; Powlson, D.; Chadwick, D.; Norse, D.; Lu, Y.-L.; Zhang, Y.; Wu, L.; et al. New technologies reduce greenhouse gas emissions from nitrogenous fertilizer in China. Proc. Natl. Acad. Sci. USA 2013, 110, 8375–8380. [Google Scholar] [CrossRef] [Green Version]
  6. Farrauto, R.J. Industrial Catalysis: A Practical Guide. In Kent and Riegel’s Handbook of Industrial Chemistry and Biotechnology; Aftalion, F., Ed.; Springer: Boston, MA, USA, 2007; pp. 271–304. [Google Scholar]
  7. Johnston, A.E.; Poulton, P.R.; Fixen, P.E.; Curtin, D. Phosphorus: Its efficient use in agriculture. In Advances in Agronomy; Sparks, D.L., Ed.; Elsevier: Amsterdam, The Netherlands, 2014; pp. 177–228. [Google Scholar]
  8. Scherer, H.W. Fertilizers and fertilization. In Encyclopedia of Soils in the Environment; Hillel, D., Ed.; Elsevier: Amsterdam, The Netherlands, 2005; pp. 20–26. [Google Scholar]
  9. Gouda, S.; Kerry, R.G.; Das, G.; Paramithiotis, S.; Shin, H.-S.; Patra, J.K. Revitalization of plant growth promoting rhizobacteria for sustainable development in agriculture. Microbiol. Res. 2018, 206, 131–140. [Google Scholar] [CrossRef]
  10. Dasgupta, D.; Kumar, K.; Miglani, R.; Mishra, R.; Panda, A.K.; Bisht, S.S. Microbial biofertilizers: Recent trends and future outlook. In Recent Advancement in Microbial Biotechnology; Elsevier: Amsterdam, The Netherlands, 2021; pp. 1–26. [Google Scholar]
  11. Singh, D.; Thapa, S.; Geat, N.; Mehriya, M.L.; Rajawat, M.V.S. Biofertilizers: Mechanisms and application. In Biofertilizers; Elsevier: Amsterdam, The Netherlands, 2021; pp. 151–166. [Google Scholar]
  12. FAO. World Fertilizer Trends and Outlook to 2020, Summary Report; Food and Agriculture Organization of the United Nations: Rome, Italy, 2017; Available online: https://www.fao.org/3/i6895e/i6895e.pdf (accessed on 10 December 2021).
  13. Chai, R.; Ye, X.; Ma, C.; Wang, Q.; Tu, R.; Zhang, L.; Gao, H. Greenhouse gas emissions from synthetic nitrogen manufacture and fertilization for main upland crops in China. Carbon Balance Manag. 2019, 14, 20. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  14. Bijay-Singh; Craswell, E. Fertilizers and nitrate pollution of surface and ground water: An increasingly pervasive global problem. SN Appl. Sci. 2021, 3, 518. [Google Scholar] [CrossRef]
  15. Lawrencia, D.; Wong, S.K.; Low, D.Y.S.; Goh, B.H.; Goh, J.K.; Ruktanonchai, U.R.; Soottitantawat, A.; Lee, L.H.; Tang, S.Y. Controlled Release Fertilizers: A Review on Coating Materials and Mechanism of Release. Plants 2021, 10, 238. [Google Scholar] [CrossRef] [PubMed]
  16. Wang, X.; Bai, J.; Xie, T.; Wang, W.; Zhang, G.; Yin, S.; Wang, D. Effects of biological nitrification inhibitors on nitrogen use efficiency and greenhouse gas emissions in agricultural soils: A review. Ecotoxicol. Environ. Saf. 2021, 220, 112338. [Google Scholar] [CrossRef]
  17. Trenkel, M.E. Improved Fertilizer Use Efficiency. Controlled-Release and Stabilized Fertilizers in Agriculture; International Fertilizer Industry Association: Paris, France, 1997. [Google Scholar]
  18. Byrne, M.P.; Tobin, J.T.; Forrestal, P.J.; Danaher, M.; Nkwonta, C.G.; Richards, K.; Cummins, E.; Hogan, S.A.; O’Callaghan, T.F. Urease and Nitrification Inhibitors—As Mitigation Tools for Greenhouse Gas Emissions in Sustainable Dairy Systems: A Review. Sustainability 2020, 12, 6018. [Google Scholar] [CrossRef]
  19. Van de Wiel, C.C.M.; van der Linden, C.G.; Scholten, O.E. Improving phosphorus use efficiency in agriculture: Opportunities for breeding. Euphytica 2016, 207, 1–22. [Google Scholar] [CrossRef] [Green Version]
  20. Bhattacharya, A. Changing Environmental Condition and Phosphorus-Use Efficiency in Plants; Elsevier: Amsterdam, The Netherlands, 2019. [Google Scholar]
  21. Bindraban, P.S.; Dimkpa, C.O.; Pandey, R. Exploring phosphorus fertilizers and fertilization strategies for improved human and environmental health. Biol. Fertil. Soils 2020, 56, 299–317. [Google Scholar] [CrossRef] [Green Version]
  22. Du Preez, C.C.; van Huyssteen, C.W.; Kotzé, E.; van Tol, J.J. Ecosystem services in sustainable food systems: Operational definition, concepts, and applications. In The Role of Ecosystem Services in Sustainable Food Systems; Rusinamhodzi, L., Ed.; Academic Press: Cambridge, MA, USA, 2020; pp. 17–42. [Google Scholar]
  23. Li, Z.; Zhang, R.; Xia, S.; Wang, L.; Liu, C.; Zhang, R.; Fan, Z.; Chen, F.; Liu, Y. Interactions between N, P and K fertilizers affect the environment and the yield and quality of satsumas. Glob. Ecol. Conserv. 2019, 19, e00663. [Google Scholar] [CrossRef]
  24. Khan, S.A.; Mulvaney, R.L.; Ellsworth, T.R. The potassium paradox: Implications for soil fertility, crop production and human health. Renew. Agric. Food Syst. 2014, 29, 3–27. [Google Scholar] [CrossRef] [Green Version]
  25. Onet, A.; Dincă, L.C.; Grenni, P.; Laslo, V.; Teusdea, A.C.; Vasile, D.L.; Enescu, R.E.; Crisan, V.E. Biological indicators for evaluating soil quality improvement in a soil degraded by erosion processes. J. Soils Sediments 2019, 19, 2393–2404. [Google Scholar] [CrossRef]
  26. Umesha, S.; Manukumar, H.M.G.; Chandrasekhar, B. Sustainable Agriculture and Food Security. In Biotechnology for Sustainable Agriculture; Singh, R.L., Mondal, S., Eds.; Woodhead Publishing: Cambridge, UK, 2018; pp. 67–92. [Google Scholar]
  27. Lewu, F.B.; Volova, T.; Thomas, S.; Rakhimol, K.R. Controlled Release Fertilizers for Sustainable Agriculture; Elsevier: Amsterdam, The Netherlands, 2021. [Google Scholar]
  28. Karthik, V.; Kumar, P.S.; Vo, D.-V.N.; Sindhu, J.; Sneka, D.; Subhashini, B.; Saravanan, K.; Jeyanthi, J. Hydrothermal production of algal biochar for environmental and fertilizer applications: A review. Environ. Chem. Lett. 2021, 19, 1025–1042. [Google Scholar] [CrossRef]
  29. Kavitha, B.; Reddy, P.V.L.; Kim, B.; Lee, S.S.; Pandey, S.K.; Kim, K.-H. Benefits and limitations of biochar amendment in agricultural soils: A review. J. Environ. Manag. 2018, 227, 146–154. [Google Scholar] [CrossRef]
  30. Juriga, M.; Šimanský, V. Effect of biochar on soil structure-review. Acta Fytotech. Zootech. 2018, 21, 11–19. [Google Scholar] [CrossRef]
  31. Mącik, M.; Gryta, A.; Frąc, M. Biofertilizers in agriculture: An overview on concepts, strategies and effects on soil microorganisms. Adv. Agron. 2020, 162, 31–87. [Google Scholar]
  32. Kumar, S.; Diksha; Sindhu, S.S.; Kumar, R. Biofertilizers: An ecofriendly technology for nutrient recycling and environmental sustainability. Curr. Res. Microb. Sci. 2022, 3, 100094. [Google Scholar] [CrossRef]
  33. Sharma, B.; Sarkar, A.; Singh, P.; Singh, R.P. Agricultural utilization of biosolids: A review on potential effects on soil and plant grown. Waste Manag. 2017, 64, 117–132. [Google Scholar] [CrossRef]
  34. Pepper, I.L.; Brooks, J.P.; Gerba, C.P. Land Application of Organic Residuals: Municipal Biosolids and Animal Manures. In Environmental and Pollution Science; Elsevier: Amsterdam, The Netherlands, 2019; pp. 419–434. [Google Scholar]
  35. Vijayakuma, S.; Saravanan, V. Biosurfactants-Types, Sources and Applications. Res. J. Microbiol. 2015, 10, 181–192. [Google Scholar] [CrossRef] [Green Version]
  36. Sachdev, D.P.; Cameotra, S.S. Biosurfactants in agriculture. Appl. Microbiol. Biotechnol. 2013, 97, 1005–1016. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  37. Tsipa, A.; Stylianou, K.; Papalli, M.; Papageorgiou, E.; Kyriakou, L.; Rigopoulos, I.; Ioannou, I.; Pinakoulaki, E. Iron-Stimulated Production and Antimicrobial Potential of a Novel Biosurfactant Produced by a Drilling Waste-Degrading Pseudomonas citronellolis Strain. Processes 2021, 9, 686. [Google Scholar] [CrossRef]
  38. Bernal, M.P.; Sommer, S.G.; Chadwick, D.; Qing, C.; Guoxue, L.; Michel, F.C. Current Approaches and Future Trends in Compost Quality Criteria for Agronomic, Environmental, and Human Health Benefits. In Advances in Agronomy; Sparks, D.L., Ed.; Academic Press: Cambridge, MA, USA, 2017; pp. 143–233. [Google Scholar]
  39. Regulation (EU) 2019/1009 of the European Parliament and of the Council of 5 June 2019 laying down rules on the making available on the market of EU fertilising products and amending Regulations (EC) No 1069/2009 and (EC) No 1107/2009 and repealing Regulation (EC) No 2003/2003. Off. J. Eur. Union 2019, L 170/1, 1–114. Available online: https://eur-lex.europa.eu/legal-content/EN/TXT/?uri=CELEX%3A32019R1009 (accessed on 18 January 2022).
  40. EC. COM(2010)235 final-Communication from the Commission to the Council and the European Parliament on Future Steps in Bio-Waste Management in the European Union; EC: Bruxelles, Belgium, 2010; Available online: https://eur-lex.europa.eu/legal-content/EN/TXT/?uri=celex%3A52010DC0235 (accessed on 18 January 2022).
  41. Weithmann, N.; Möller, J.N.; Löder, M.G.J.; Piehl, S.; Laforsch, C.; Freitag, R. Organic fertilizer as a vehicle for the entry of microplastic into the environment. Sci. Adv. 2018, 4, eaap8060. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  42. Visca, A.; Barra Caracciolo, A.; Grenni, P.; Patrolecco, L.; Rauseo, J.; Massini, G.; Miritana, V.M.; Spataro, F. Anaerobic digestion and removal of sulfamethoxazole, enrofloxacin, ciprofloxacin and their antibiotic resistance genes in a full-scale biogas plant. Antibiotics 2021, 10, 502. [Google Scholar] [CrossRef] [PubMed]
  43. Visca, A.; Rauseo, J.; Spataro, F.; Patrolecco, L.; Grenni, P.; Massini, G.; Mazzurco Miritana, V.; Barra Caracciolo, A. Antibiotics and antibiotic resistance genes in anaerobic digesters and predicted concentrations in agroecosystems. J. Environ. Manag. 2022, 301, 113891. [Google Scholar] [CrossRef] [PubMed]
  44. Loyon, L. Overview of Animal Manure Management for Beef, Pig, and Poultry Farms in France. Front. Sustain. Food Syst. 2018, 2, 2. [Google Scholar] [CrossRef]
  45. Barra Caracciolo, A.; Visca, A.; Massini, G.; Patrolecco, L.; Miritana, V.M.; Grenni, P. Environmental Fate of Antibiotics and Resistance Genes in Livestock Waste and Digestate from Biogas Plants. Environ. Sci. Pollut. Res. Manag. 2020, 2020, ESPRM-102. [Google Scholar] [CrossRef]
  46. Miritana, V.M.; Massini, G.; Visca, A.; Grenni, P.; Patrolecco, L.; Spataro, F.; Rauseo, J.; Garbini, G.L.; Signorini, A.; Rosa, S.; et al. Effects of Sulfamethoxazole on the Microbial Community Dynamics During the Anaerobic Digestion Process. Front. Microbiol. 2020, 11, 537783. [Google Scholar] [CrossRef]
  47. Rayne, N.; Aula, L. Livestock Manure and the Impacts on Soil Health: A Review. Soil Syst. 2020, 4, 64. [Google Scholar] [CrossRef]
  48. Mupambwa, H.A.; Mnkeni, P.N.S. Optimizing the vermicomposting of organic wastes amended with inorganic materials for production of nutrient-rich organic fertilizers: A review. Environ. Sci. Pollut. Res. 2018, 25, 10577–10595. [Google Scholar] [CrossRef] [PubMed]
  49. Ali, U.; Sajid, N.; Khalid, A.; Riaz, L.; Rabbani, M.M.; Syed, J.H.; Malik, R.N. A review on vermicomposting of organic wastes. Environ. Prog. Sustain. Energy 2015, 34, 1050–1062. [Google Scholar] [CrossRef]
  50. Sulaiman, I.S.C.; Mohamad, A. The Use of Vermiwash and Vermicompost Extract in Plant Disease and Pest Control. In Natural Remedies for Pest, Disease and Weed Control; Elsevier: Amsterdam, The Netherlands, 2020; pp. 187–201. [Google Scholar]
  51. Sharma, K.; Garg, V.K. Vermicomposting: A Green Technology for Organic Waste Management. In Waste to Wealth. Energy, Environment, and Sustainability; Singhania, R., Agarwal, R., Kumar, R., Sukumaran, R., Eds.; Springer: Singapore, 2018; pp. 199–235. [Google Scholar]
  52. FAO; ITPS; GSBI; SCBD, EC. State of Knowledge of Soil Biodiversity–Status, Challenges and Potentialities. Summary for Policy Makers; FAO: Rome, Italy, 2020; ISBN 978-92-5-133583-3. Available online: https://www.fao.org/3/cb1928en/cb1928en.pdf (accessed on 18 January 2022).
  53. Mercado-Blanco, J.; Abrantes, I.; Barra Caracciolo, A.; Bevivino, A.; Ciancio, A.; Grenni, P.; Hrynkiewicz, K.; Kredics, L.; Proença, D.N. Belowground microbiota and the health of tree crops. Front. Microbiol. 2018, 9, 1006. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  54. Barra Caracciolo, A.; Grenni, P. Bio-remediation of soil ecosystems from triazine herbicides. In Pesticides in Soils: Occurrence, Fate, Control and Remediation; Rodríguez-Cruz, M., Sánchez-Martín, M., Eds.; Springer: Berlin/Heidelberg, Germany, 2021. [Google Scholar]
  55. Saleem, M.; Hu, J.; Jousset, A. More Than the Sum of Its Parts: Microbiome Biodiversity as a Driver of Plant Growth and Soil Health. Annu. Rev. Ecol. Evol. Syst. 2019, 50, 145–168. [Google Scholar] [CrossRef]
  56. Paz-Ferreiro, J.; Fu, S. Biological Indices for Soil Quality Evaluation: Perspectives and Limitations. Land Degrad. Dev. 2016, 27, 14–25. [Google Scholar] [CrossRef]
  57. Singh, J.S.; Gupta, V.K. Soil microbial biomass: A key soil driver in management of ecosystem functioning. Sci. Total Environ. 2018, 634, 497–500. [Google Scholar] [CrossRef]
  58. Schloter, M.; Nannipieri, P.; Sørensen, S.J.; van Elsas, J.D. Microbial indicators for soil quality. Biol. Fertil. Soils 2018, 54, 1–10. [Google Scholar] [CrossRef] [Green Version]
  59. Doran, J.W.; Zeiss, M.R. Soil health and sustainability: Managing the biotic component of soil quality. Appl. Soil Ecol. 2000, 15, 3–11. [Google Scholar] [CrossRef] [Green Version]
  60. Karlen, D.L.; Mausbach, M.J.; Doran, J.W.; Cline, R.G.; Harris, R.F.; Schuman, G.E. Soil Quality: A Concept, Definition, and Framework for Evaluation. Soil Sci. Soc. Am. J. 1997, 61, 4–10. [Google Scholar] [CrossRef] [Green Version]
  61. Hartmann, M.; Frey, B.; Mayer, J.; Mäder, P.; Widmer, F. Distinct soil microbial diversity under long-term organic and conventional farming. ISME J. 2015, 9, 1177–1194. [Google Scholar] [CrossRef] [Green Version]
  62. Cai, F.; Pang, G.; Li, R.-X.; Li, R.; Gu, X.-L.; Shen, Q.-R.; Chen, W. Bioorganic fertilizer maintains a more stable soil microbiome than chemical fertilizer for monocropping. Biol. Fertil. Soils 2017, 53, 861–872. [Google Scholar] [CrossRef]
  63. Oneț, A.; Teușdea, A.; Boja, N.; Domuța, C.; Oneț, C. Effects of common oak (Quercus robur L.) defolition on the soil properties of an oak forest in Western Plain of Romania. Ann. For. Res. 2016, 59, 1. [Google Scholar] [CrossRef] [Green Version]
  64. FAO. Keep Soil Alive, Protect Soil Biodiversity–Global Symposium on Soil Biodiversity 19–22 April 2021. Proceedings; Food and Agriculture Organization of the United Nations: Rome, Italy, 2021; Available online: https://www.fao.org/documents/card/en/c/cb6005en (accessed on 18 January 2022).
  65. EU. COM(2021) 699 Final, Communication from the Commission to the European Parliament, the Council, the European Economic and Social Committee and the Committee of the Regions EU Soil Strategy for 2030 Reaping the Benefits of Healthy Soils for People, Food, Nature and Climate; EU: Bruxelles, Belgium, 2021; Available online: https://eur-lex.europa.eu/legal-content/EN/TXT/?uri=CELEX%3A52021DC0699 (accessed on 18 January 2022).
  66. Onet, A.; Cimpeanu, C.; Teusdea, A.; Pantea, S.; Modog, T. Evaluation of the Soil Properties Variability in Relation to Different Crop Types. J. Environ. Prot. Ecol. 2016, 17, 1305–1314. [Google Scholar]
  67. Nannipieri, P.; Kandeler, E.; Ruggiero, P. Enzyme activities and microbiological and biochemical processes in soil. In Enzymes in the Environment: Activity, Ecology and Applications; Burns, R.G., Dick, R.P., Eds.; Marcel Dekker: New York, NY, USA, 2002; pp. 1–33. ISBN 0-8247-0614-5. [Google Scholar]
  68. Nannipieri, P.; Trasar-Cepeda, C.; Dick, R.P. Soil enzyme activity: A brief history and biochemistry as a basis for appropriate interpretations and meta-analysis. Biol. Fertil. Soils 2018, 54, 11–19. [Google Scholar] [CrossRef]
  69. Heyn, P.C.; Meeks, S.; Pruchno, R. Methodological Guidance for a Quality Review Article. Gerontologist 2019, 59, 197–201. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  70. Mandic, L.; Djukić, D.; Beatovic, I.; Jovovic, Z.; Pesakovic, M.; Stevovic, V. Effect of different fertilizers on the microbial activity and productivity of soil under potato cultivation. Afr. J. Biotechnol. 2011, 10, 6954–6960. [Google Scholar]
  71. Chu, H.; Lin, X.; Fujii, T.; Morimoto, S.; Yagi, K.; Hu, J.; Zhang, J. Soil microbial biomass, dehydrogenase activity, bacterial community structure in response to long-term fertilizer management. Soil Biol. Biochem. 2007, 39, 2971–2976. [Google Scholar] [CrossRef]
  72. Joergensen, R.G.; Mäder, P.; Fließbach, A. Long-term effects of organic farming on fungal and bacterial residues in relation to microbial energy metabolism. Biol. Fertil. Soils 2010, 46, 303–307. [Google Scholar] [CrossRef]
  73. Murugan, R.; Kumar, S. Influence of long-term fertilisation and crop rotation on changes in fungal and bacterial residues in a tropical rice-field soil. Biol. Fertil. Soils 2013, 49, 847–856. [Google Scholar] [CrossRef]
  74. Tao, R.; Liang, Y.; Wakelin, S.A.; Chu, G. Supplementing chemical fertilizer with an organic component increases soil biological function and quality. Appl. Soil Ecol. 2015, 96, 42–51. [Google Scholar] [CrossRef]
  75. Li, J.; Zhao, B.; Li, X.; Jiang, R.; Bing, S.H. Effects of Long-Term Combined Application of Organic and Mineral Fertilizers on Microbial Biomass, Soil Enzyme Activities and Soil Fertility. Agric. Sci. China 2008, 7, 336–343. [Google Scholar] [CrossRef]
  76. Francioli, D.; Schulz, E.; Lentendu, G.; Wubet, T.; Buscot, F.; Reitz, T. Mineral vs. Organic Amendments: Microbial Community Structure, Activity and Abundance of Agriculturally Relevant Microbes Are Driven by Long-Term Fertilization Strategies. Front. Microbiol. 2016, 7, 1446. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  77. Geisseler, D.; Scow, K.M. Long-term effects of mineral fertilizers on soil microorganisms–A review. Soil Biol. Biochem. 2014, 75, 54–63. [Google Scholar] [CrossRef]
  78. Wang, F.; Han, W.; Chen, S.; Dong, W.; Qiao, M.; Hu, C.; Liu, B. Fifteen-Year Application of Manure and Chemical Fertilizers Differently Impacts Soil ARGs and Microbial Community Structure. Front. Microbiol. 2020, 11, 62. [Google Scholar] [CrossRef] [PubMed]
  79. Cai, F.; Luo, P.; Yang, J.; Irfan, M.; Zhang, S.; An, N.; Dai, J.; Han, X. Effect of Long-Term Fertilization on Ammonia-Oxidizing Microorganisms and Nitrification in Brown Soil of Northeast China. Front. Microbiol. 2021, 11, 622454. [Google Scholar] [CrossRef] [PubMed]
  80. Kang, G.S.; Beri, V.; Sidhu, B.S.; Rupela, O.P. A new index to assess soil quality and sustainability of wheat-based cropping systems. Biol. Fertil. Soils 2005, 41, 389–398. [Google Scholar] [CrossRef] [Green Version]
  81. Nakhro, N.; Dkhar, M.S. Populations and biomass carbon in paddy field soil. J. Agron. 2010, 9, 102–110. [Google Scholar] [CrossRef] [Green Version]
  82. Sun, R.; Guo, X.; Wang, D.; Chu, H. Effects of long-term application of chemical and organic fertilizers on the abundance of microbial communities involved in the nitrogen cycle. Appl. Soil Ecol. 2015, 95, 171–178. [Google Scholar] [CrossRef]
  83. Cui, J.; Yuan, X.; Zhang, Q.; Zhou, J.; Lin, K.; Xu, J.; Zeng, Y.; Wu, Y.; Cheng, L.; Zeng, Q.; et al. Nutrient availability is a dominant predictor of soil bacterial and fungal community composition after nitrogen addition in subtropical acidic forests. PLoS ONE 2021, 16, e0246263. [Google Scholar] [CrossRef]
  84. Wang, J.L.; Liu, K.L.; Zhao, X.Q.; Zhang, H.Q.; Li, D.; Li, J.J.; Shen, R.F. Balanced fertilization over four decades has sustained soil microbial communities and improved soil fertility and rice productivity in red paddy soil. Sci. Total Environ. 2021, 793, 148664. [Google Scholar] [CrossRef]
  85. Goyal, S.; Mishra, M.M.; Hooda, I.S.; Singh, R. Organic matter-microbial biomass relationships in field experiments under tropical conditions: Effects of inorganic fertilization and organic amendments. Soil Biol. Biochem. 1992, 24, 1081–1084. [Google Scholar] [CrossRef]
  86. Ai, C.; Zhang, S.; Zhang, X.; Guo, D.; Zhou, W.; Huang, S. Distinct responses of soil bacterial and fungal communities to changes in fertilization regime and crop rotation. Geoderma 2018, 319, 156–166. [Google Scholar] [CrossRef]
  87. Cassman, N.A.; Leite, M.F.A.; Pan, Y.; de Hollander, M.; van Veen, J.A.; Kuramae, E.E. Plant and soil fungal but not soil bacterial communities are linked in long-term fertilized grassland. Sci. Rep. 2016, 6, 23680. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  88. Ren, J.; Liu, X.; Yang, W.; Yang, X.; Li, W.; Xia, Q.; Li, J.; Gao, Z.; Yang, Z. Rhizosphere soil properties, microbial community, and enzyme activities: Short-term responses to partial substitution of chemical fertilizer with organic manure. J. Environ. Manag. 2021, 299, 113650. [Google Scholar] [CrossRef] [PubMed]
  89. Benizri, E.; Amiaud, B. Relationship between plants and soil microbial communities in fertilized grasslands. Soil Biol. Biochem. 2005, 37, 2055–2064. [Google Scholar] [CrossRef]
  90. Luo, P.; Han, X.; Wang, Y.; Han, M.; Shi, H.; Liu, N.; Bai, H. Influence of long-term fertilization on soil microbial biomass, dehydrogenase activity, and bacterial and fungal community structure in a brown soil of northeast China. Ann. Microbiol. 2015, 65, 533–542. [Google Scholar] [CrossRef] [Green Version]
  91. Zhang, W.J.; Wang, X.J.; Xu, M.G.; Huang, S.M.; Liu, H.; Peng, C. Soil organic carbon dynamics under long-term fertilizations in arable land of northern China. Biogeosciences 2010, 7, 409–425. [Google Scholar] [CrossRef] [Green Version]
  92. Aref, S.; Wander, M.M. Long-Term Trends of Corn Yield and Soil Organic Matter in Different Crop Sequences and Soil Fertility Treatments on the Morrow Plots. In Advances in Agronomy; Sparks, D.L., Ed.; Academic Press: Cambridge, MA, USA, 1997; pp. 153–197. [Google Scholar]
  93. Guo, Z.; Han, J.; Li, J.; Xu, Y.; Wang, X. Effects of long-term fertilization on soil organic carbon mineralization and microbial community structure. PLoS ONE 2019, 14, e0211163. [Google Scholar] [CrossRef] [Green Version]
  94. Yang, F.; Tian, J.; Fang, H.; Gao, Y.; Xu, M.; Lou, Y.; Zhou, B.; Kuzyakov, Y. Functional Soil Organic Matter Fractions, Microbial Community, and Enzyme Activities in a Mollisol Under 35 Years Manure and Mineral Fertilization. J. Soil Sci. Plant Nutr. 2019, 19, 430–439. [Google Scholar] [CrossRef]
  95. Tian, J.; Lou, Y.; Gao, Y.; Fang, H.; Liu, S.; Xu, M.; Blagodatskaya, E.; Kuzyakov, Y. Response of soil organic matter fractions and composition of microbial community to long-term organic and mineral fertilization. Biol. Fertil. Soils 2017, 53, 523–532. [Google Scholar] [CrossRef]
  96. Cookson, W.R.; Abaye, D.A.; Marschner, P.; Murphy, D.V.; Stockdale, E.A.; Goulding, K.W.T. The contribution of soil organic matter fractions to carbon and nitrogen mineralization and microbial community size and structure. Soil Biol. Biochem. 2005, 37, 1726–1737. [Google Scholar] [CrossRef]
  97. Luo, G.; Friman, V.-P.; Chen, H.; Liu, M.; Wang, M.; Guo, S.; Ling, N.; Shen, Q. Long-term fertilization regimes drive the abundance and composition of N-cycling-related prokaryotic groups via soil particle-size differentiation. Soil Biol. Biochem. 2018, 116, 213–223. [Google Scholar] [CrossRef]
  98. Šimek, M.; Hopkins, D.W.; Kalčík, J.; Picek, T.; Šantrůčková, H.; Staňa, J.; Trávník, K. Biological and chemical properties of arable soils affected by long-term organic and inorganic fertilizer applications. Biol. Fertil. Soils 1999, 29, 300–308. [Google Scholar] [CrossRef]
  99. Perrott, K.; Sarathchandra, S.; Dow, B. Seasonal and fertilizer effects on the organic cycle and microbial biomass in a hill country soil under pasture. Soil Res. 1992, 30, 383. [Google Scholar] [CrossRef]
  100. Fraser, P.M.; Haynes, R.J.; Williams, P.H. Effects of pasture improvement and intensive cultivation on microbial biomass, enzyme activities, and composition and size of earthworm populations. Biol. Fertil. Soils 1994, 17, 185–190. [Google Scholar] [CrossRef]
  101. Dhull, S.; Goyal, S.; Kapoor, K.; Mundra, M. Microbial biomass carbon and microbial activities of soils receiving chemical fertilizers and organic amendments. Arch. Agron. Soil Sci. 2004, 50, 641–647. [Google Scholar] [CrossRef]
  102. Bera, T.; Collins, H.P.; Alva, A.K.; Purakayastha, T.J.; Patra, A.K. Biochar and manure effluent effects on soil biochemical properties under corn production. Appl. Soil Ecol. 2016, 107, 360–367. [Google Scholar] [CrossRef]
  103. Mi, W.; Sun, Y.; Xia, S.; Zhao, H.; Mi, W.; Brookes, P.C.; Liu, Y.; Wu, L. Effect of inorganic fertilizers with organic amendments on soil chemical properties and rice yield in a low-productivity paddy soil. Geoderma 2018, 320, 23–29. [Google Scholar] [CrossRef]
  104. Nannipieri, P.; Ascher, J.; Ceccherini, M.T.; Landi, L.; Pietramellara, G.; Renella, G. Microbial diversity and soil functions. Eur. J. Soil Sci. 2003, 54, 655–670. [Google Scholar] [CrossRef]
  105. Blake, L.; Mercik, S.; Koerschens, M.; Moskal, S.; Poulton, P.R.; Goulding, K.W.T.; Weigel, A.; Powlson, D.S. Phosphorus content in soil, uptake by plants and balance in three European long-term field experiments. Nutr. Cycl. Agroecosyst. 2000, 56, 263–275. [Google Scholar] [CrossRef]
  106. Liu, A.; Hamel, C.; Spedding, T.; Zhang, T.-Q.; Mongeau, R.; Lamarre, G.R.; Tremblay, G. Soil microbial carbon and phosphorus as influenced by phosphorus fertilization and tillage in a maize-soybean rotation in south-western Quebec. Can. J. Soil Sci. 2008, 88, 21–30. [Google Scholar] [CrossRef]
  107. Beauregard, M.S.; Hamel, C.; Atul-Nayyar; St-Arnaud, M. Long-Term Phosphorus Fertilization Impacts Soil Fungal and Bacterial Diversity but not AM Fungal Community in Alfalfa. Microb. Ecol. 2010, 59, 379–389. [Google Scholar] [CrossRef] [PubMed]
  108. Enebe, M.C.; Babalola, O.O. Effects of inorganic and organic treatments on the microbial community of maize rhizosphere by a shotgun metagenomics approach. Ann. Microbiol. 2020, 70, 49. [Google Scholar] [CrossRef]
  109. Zhan, Y.; Liu, W.; Bao, Y.; Zhang, J.; Petropoulos, E.; Li, Z.; Lin, X.; Feng, Y. Fertilization shapes a well-organized community of bacterial decomposers for accelerated paddy straw degradation. Sci. Rep. 2018, 8, 7981. [Google Scholar] [CrossRef]
  110. Song, Z.; Gao, H.; Zhu, P.; Peng, C.; Deng, A.; Zheng, C.; Mannaf, M.A.; Islam, M.N.; Zhang, W. Organic amendments increase corn yield by enhancing soil resilience to climate change. Crop J. 2015, 3, 110–117. [Google Scholar] [CrossRef] [Green Version]
  111. Pan, H.; Chen, M.; Feng, H.; Wei, M.; Song, F.; Lou, Y.; Cui, X.; Wang, H.; Zhuge, Y. Organic and inorganic fertilizers respectively drive bacterial and fungal community compositions in a fluvo-aquic soil in northern China. Soil Tillage Res. 2020, 198, 104540. [Google Scholar] [CrossRef]
  112. He, J.-Z.; Zheng, Y.; Chen, C.-R.; He, Y.-Q.; Zhang, L.-M. Microbial composition and diversity of an upland red soil under long-term fertilization treatments as revealed by culture-dependent and culture-independent approaches. J. Soils Sediments 2008, 8, 349–358. [Google Scholar] [CrossRef]
  113. Edmeades, D.C. The long-term effects of manures and fertilisers on soil productivity and quality: A review. Nutr. Cycl. Agroecosyst. 2003, 66, 165–180. [Google Scholar] [CrossRef]
  114. De Vries, F.T.; Hoffland, E.; van Eekeren, N.; Brussaard, L.; Bloem, J. Fungal/bacterial ratios in grasslands with contrasting nitrogen management. Soil Biol. Biochem. 2006, 38, 2092–2103. [Google Scholar] [CrossRef] [Green Version]
  115. Ju, X.; Liu, X.; Zhang, F.; Roelcke, M. Nitrogen Fertilization, Soil Nitrate Accumulation, and Policy Recommendations in Several Agricultural Regions of China. AMBIO A J. Hum. Environ. 2004, 33, 300–305. [Google Scholar] [CrossRef]
  116. Cruz, A.F.; Hamel, C.; Hanson, K.; Selles, F.; Zentner, R.P. Thirty-seven years of soil nitrogen and phosphorus fertility management shapes the structure and function of the soil microbial community in a Brown Chernozem. Plant Soil 2009, 315, 173–184. [Google Scholar] [CrossRef]
  117. Gu, Y.; Zhang, X.; Tu, S.; Lindström, K. Soil microbial biomass, crop yields, and bacterial community structure as affected by long-term fertilizer treatments under wheat-rice cropping. Eur. J. Soil Biol. 2009, 45, 239–246. [Google Scholar] [CrossRef]
  118. Hyman, M.R.; Kim, C.Y.; Arp, D.J. Inhibition of ammonia monooxygenase in Nitrosomonas europaea by carbon disulfide. J. Bacteriol. 1990, 172, 4775–4782. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  119. Zydlik, Z.; Pacholak, E. Effect of soil fatigue prevention methods on microbiological soil status in replanted apple tree orchard. Part III. Number of fungi and Actinomycetes. Electron. J. Polish Agric. Univ. 2006, 9, #58. Available online: http://www.ejpau.media.pl/volume9/issue4/art-58.html (accessed on 18 January 2022).
  120. Ashworth, A.J.; DeBruyn, J.M.; Allen, F.L.; Radosevich, M.; Owens, P.R. Microbial community structure is affected by cropping sequences and poultry litter under long-term no-tillage. Soil Biol. Biochem. 2017, 114, 210–219. [Google Scholar] [CrossRef]
  121. Cui, X.; Zhang, Y.; Gao, J.; Peng, F.; Gao, P. Long-term combined application of manure and chemical fertilizer sustained higher nutrient status and rhizospheric bacterial diversity in reddish paddy soil of Central South China. Sci. Rep. 2018, 8, 16554. [Google Scholar] [CrossRef]
  122. Dijksterhuis, J.; Samson, R.A. Zygomycetes. In Woodhead Publishing Series in Food Science, Technology and Nutrition, Food Spoilage Microorganisms; Blackburn, C.d.W., Ed.; Woodhead Publishing: Cambridge, UK, 2006; pp. 415–436. [Google Scholar]
  123. Rieke, E.L.; Soupir, M.L.; Moorman, T.B.; Yang, F.; Howe, A.C. Temporal Dynamics of Bacterial Communities in Soil and Leachate Water After Swine Manure Application. Front. Microbiol. 2018, 9, 3197. [Google Scholar] [CrossRef] [Green Version]
  124. Ouyang, Y.; Reeve, J.R.; Norton, J.M. Soil enzyme activities and abundance of microbial functional genes involved in nitrogen transformations in an organic farming system. Biol. Fertil. Soils 2018, 54, 437–450. [Google Scholar] [CrossRef]
  125. Tao, R.; Wakelin, S.A.; Liang, Y.; Chu, G. Response of ammonia-oxidizing archaea and bacteria in calcareous soil to mineral and organic fertilizer application and their relative contribution to nitrification. Soil Biol. Biochem. 2017, 114, 20–30. [Google Scholar] [CrossRef]
  126. Zou, W.; Lang, M.; Zhang, L.; Liu, B.; Chen, X. Ammonia-oxidizing bacteria rather than ammonia-oxidizing archaea dominate nitrification in a nitrogen-fertilized calcareous soil. Sci. Total Environ. 2021, 811, 151402. [Google Scholar] [CrossRef] [PubMed]
  127. Koch, A.L. Oligotrophs versus copiotrophs. BioEssays 2001, 23, 657–661. [Google Scholar] [CrossRef] [PubMed]
  128. Yao, F.; Yang, S.; Wang, Z.; Wang, X.; Ye, J.; Wang, X.; DeBruyn, J.M.; Feng, X.; Jiang, Y.; Li, H. Microbial Taxa Distribution Is Associated with Ecological Trophic Cascades along an Elevation Gradient. Front. Microbiol. 2017, 8, 2071. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  129. Parham, J.A.; Deng, S.P.; Da, H.N.; Sun, H.Y.; Raun, W.R. Long-term cattle manure application in soil. II. Effect on soil microbial populations and community structure. Biol. Fertil. Soils 2003, 38, 209–215. [Google Scholar] [CrossRef]
  130. Song, H.-K.; Song, W.; Kim, M.; Tripathi, B.M.; Kim, H.; Jablonski, P.; Adams, J.M. Bacterial strategies along nutrient and time gradients, revealed by metagenomic analysis of laboratory microcosms. FEMS Microbiol. Ecol. 2017, 93, fix114. [Google Scholar] [CrossRef]
  131. Wang, Z.; Wang, Z.; Li, T.; Wang, C.; Dang, N.; Wang, R.; Jiang, Y.; Wang, H.; Li, H. N and P fertilization enhanced carbon decomposition function by shifting microbes towards an r-selected community in meadow grassland soils. Ecol. Indic. 2021, 132, 108306. [Google Scholar] [CrossRef]
  132. Sumbul, A.; Ansari, R.A.; Rizvi, R.; Mahmood, I. Azotobacter: A potential bio-fertilizer for soil and plant health management. Saudi J. Biol. Sci. 2020, 27, 3634–3640. [Google Scholar] [CrossRef]
  133. Styła, K.; Sawicka, A. Microbiological activity of soil against the background of differentiated irrigation and fertilization in apple (Malus domestica) orchard after replantation. Agron. Res. 2010, 8, 827–836. [Google Scholar]
  134. Cinnadurai, C.; Gopalaswamy, G.; Balachandar, D. Diversity of cultivable Azotobacter in the semi-arid alfisol receiving long-term organic and inorganic nutrient amendments. Ann. Microbiol. 2013, 63, 1397–1404. [Google Scholar] [CrossRef]
  135. Adediran, J.A.; De Baets, N.; Mnkeni, P.N.S.; Kiekens, L.; Muyima, N.Y.O.; Thys, A. Organic Waste Materials for Soil Fertility Improvement in the Border Region of the Eastern Cape, South Africa. Biol. Agric. Hortic. 2003, 20, 283–300. [Google Scholar] [CrossRef]
  136. Bokhtiar, S.M.; Paul, G.C.; Alam, K.M. Effects of Organic and Inorganic Fertilizer on Growth, Yield, and Juice Quality and Residual Effects on Ratoon Crops of Sugarcane. J. Plant Nutr. 2008, 31, 1832–1843. [Google Scholar] [CrossRef]
  137. Schauss, K.; Focks, A.; Leininger, S.; Kotzerke, A.; Heuer, H.; Thiele-Bruhn, S.; Sharma, S.; Wilke, B.-M.; Matthies, M.; Smalla, K.; et al. Dynamics and functional relevance of ammonia-oxidizing archaea in two agricultural soils. Environ. Microbiol. 2009, 11, 446–456. [Google Scholar] [CrossRef] [PubMed]
  138. Chen, X.; Zhang, L.-M.; Shen, J.-P.; Wei, W.-X.; He, J.-Z. Abundance and community structure of ammonia-oxidizing archaea and bacteria in an acid paddy soil. Biol. Fertil. Soils 2011, 47, 323–331. [Google Scholar] [CrossRef]
  139. Ge, Y.; Zhang, J.; Zhang, L.; Yang, M.; He, J. Long-term fertilization regimes affect bacterial community structure and diversity of an agricultural soil in northern China. J. Soils Sediments 2008, 8, 43–50. [Google Scholar] [CrossRef]
  140. Da Silva, P.; Nahas, E. Bacterial diversity in soil in response to different plans, phosphate fertilizers and liming. Braz. J. Microbiol. 2002, 33, 304–310. [Google Scholar] [CrossRef] [Green Version]
  141. Zhao, J.; Ni, T.; Li, J.; Lu, Q.; Fang, Z.; Huang, Q.; Zhang, R.; Li, R.; Shen, B.; Shen, Q. Effects of organic–inorganic compound fertilizer with reduced chemical fertilizer application on crop yields, soil biological activity and bacterial community structure in a rice–wheat cropping system. Appl. Soil Ecol. 2016, 99, 1–12. [Google Scholar] [CrossRef]
  142. Liang, R.; Hou, R.; Li, J.; Lyu, Y.; Hang, S.; Gong, H.; Ouyang, Z. Effects of Different Fertilizers on Rhizosphere Bacterial Communities of Winter Wheat in the North China Plain. Agronomy 2020, 10, 93. [Google Scholar] [CrossRef] [Green Version]
  143. Maeder, P.; Fliessbach, A.; Dubois, D.; Gunst, L.; Fried, P.; Niggli, U. Soil Fertility and Biodiversity in Organic Farming. Science 2002, 296, 1694–1697. [Google Scholar] [CrossRef] [Green Version]
  144. Bulluck, L.R.; Ristaino, J.B. Effect of Synthetic and Organic Soil Fertility Amendments on Southern Blight, Soil Microbial Communities, and Yield of Processing Tomatoes. Phytopathology 2002, 92, 181–189. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  145. Liu, B.; Gumpertz, M.L.; Hu, S.; Ristaino, J.B. Long-term effects of organic and synthetic soil fertility amendments on soil microbial communities and the development of southern blight. Soil Biol. Biochem. 2007, 39, 2302–2316. [Google Scholar] [CrossRef]
  146. Moharana, P.C.; Sharma, B.M.; Biswas, D.R. Changes in the soil properties and availability of micronutrients after six-year application of organic and chemical fertilizers using STCR-based targeted yield equations under pearl millet-wheat cropping system. J. Plant Nutr. 2017, 40, 165–176. [Google Scholar] [CrossRef]
  147. Jenkinson, D.S. The Rothamsted Long-Term Experiments: Are They Still of Use? Agron. J. 1991, 83, 2–10. [Google Scholar] [CrossRef]
  148. Birkhofer, K.; Bezemer, T.M.; Bloem, J.; Bonkowski, M.; Christensen, S.; Dubois, D.; Ekelund, F.; Fließbach, A.; Gunst, L.; Hedlund, K.; et al. Long-term organic farming fosters below and aboveground biota: Implications for soil quality, biological control and productivity. Soil Biol. Biochem. 2008, 40, 2297–2308. [Google Scholar] [CrossRef]
  149. Ayoola, O.; Adeniyan, O. Influence of poultry manure and NPK fertilizer on yield and yield components of crops under different cropping systems in south west Nigeria. Afr. J. Biotechnol. 2006, 5, 1386–1392. [Google Scholar]
  150. Schjønning, P.; Jensen, J.L.; Bruun, S.; Jensen, L.S.; Christensen, B.T.; Munkholm, L.J.; Oelofse, M.; Baby, S.; Knudsen, L. The Role of Soil Organic Matter for Maintaining Crop Yields: Evidence for a Renewed Conceptual Basis. In Advances in Agronomy; Sparks, D.L., Ed.; Academic Press: Cambridge, MA, USA, 2018; pp. 35–79. [Google Scholar]
  151. Ledgard, S.; De Klein, C.; Crush, J.; Thorrold, B. Dairy farming, nitrogen losses and nitrate-sensitive areas. In Proceedings of the New Zealand Society of Animal Production, Mosgiel, New Zealand; 2000; pp. 256–260. Available online: http://www.nzsap.org/system/files/proceedings/2000/ab00066.pdf (accessed on 18 January 2022).
  152. Sims, J.T.; Wolf, D.C. Poultry Waste Management: Agricultural and Environmental Issues. Adv. Agron. 1994, 52, 1–83. [Google Scholar] [CrossRef]
  153. Graetz, D.A.; Nair, V.D. Fate of phosphorus in Florida Spodosols contaminated with cattle manure. Ecol. Eng. 1995, 5, 163–181. [Google Scholar] [CrossRef]
  154. Ullah, S.; Ai, C.; Huang, S.; Zhang, J.; Jia, L.; Ma, J.; Zhou, W.; He, P. The responses of extracellular enzyme activities and microbial community composition under nitrogen addition in an upland soil. PLoS ONE 2019, 14, e0223026. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  155. Marschner, P. Structure and function of the soil microbial community in a long-term fertilizer experiment. Soil Biol. Biochem. 2003, 35, 453–461. [Google Scholar] [CrossRef]
  156. Dangi, S.; Gao, S.; Duan, Y.; Wang, D. Soil microbial community structure affected by biochar and fertilizer sources. Appl. Soil Ecol. 2020, 150, 103452. [Google Scholar] [CrossRef]
  157. Chen, L.; Wang, X.; Zhou, W.; Guo, S.; Zhu, R.; Qin, Y.; Sun, J. Responses of crop yields, soil enzymatic activities, and microbial communities to different long-term organic materials applied with chemical fertilizer in purple soil. Eur. J. Soil Biol. 2021, 105, 103319. [Google Scholar] [CrossRef]
  158. Yang, Y.; Li, G.; Min, K.; Liu, T.; Li, C.; Xu, J.; Hu, F.; Li, H. The potential role of fertilizer-derived exogenous bacteria on soil bacterial community assemblage and network formation. Chemosphere 2022, 287, 132338. [Google Scholar] [CrossRef]
  159. Bonanomi, G.; De Filippis, F.; Zotti, M.; Idbella, M.; Cesarano, G.; Al-Rowaily, S.; Abd-ElGawad, A. Repeated applications of organic amendments promote beneficial microbiota, improve soil fertility and increase crop yield. Appl. Soil Ecol. 2020, 156, 103714. [Google Scholar] [CrossRef]
  160. Anwar, M.; Patra, D.D.; Chand, S.; Alpesh, K.; Naqvi, A.A.; Khanuja, S.P.S. Effect of Organic Manures and Inorganic Fertilizer on Growth, Herb and Oil Yield, Nutrient Accumulation, and Oil Quality of French Basil. Commun. Soil Sci. Plant Anal. 2005, 36, 1737–1746. [Google Scholar] [CrossRef]
  161. Kaur, K.; Kapoor, K.K.; Gupta, A.P. Impact of organic manures with and without mineral fertilizers on soil chemical and biological properties under tropical conditions. J. Plant Nutr. Soil Sci. 2005, 168, 117–122. [Google Scholar] [CrossRef]
  162. Masto, R.E.; Chhonkar, P.K.; Singh, D.; Patra, A.K. Changes in soil biological and biochemical characteristics in a long-term field trial on a sub-tropical inceptisol. Soil Biol. Biochem. 2006, 38, 1577–1582. [Google Scholar] [CrossRef]
  163. Zhang, Q.-C.; Shamsi, I.H.; Xu, D.-T.; Wang, G.-H.; Lin, X.-Y.; Jilani, G.; Hussain, N.; Chaudhry, A.N. Chemical fertilizer and organic manure inputs in soil exhibit a vice versa pattern of microbial community structure. Appl. Soil Ecol. 2012, 57, 1–8. [Google Scholar] [CrossRef]
  164. Corbu, V.; Csutak, O. Candida-produced biosurfactants-beneficial agents for environmental remediation biotechnologies. Rom. Biotechnol. Lett. 2019, 24, 381–387. [Google Scholar] [CrossRef]
  165. Gomaa, E.Z. Biosequestration of heavy metals by microbially induced calcite precipitation of ureolytic bacteria. Rom. Biotechnol. Lett. 2019, 24, 147–153. Available online: https://www.rombio.eu/docs/Biosequestration%20of%20heavy%20metals%20by%20microbially%20induced%20calcite%20precipitation%20of%20ureolytic%20bacteria.pdf (accessed on 18 January 2022). [CrossRef]
  166. Chirinda, N.; Olesen, J.E.; Porter, J.R.; Schjønning, P. Soil properties, crop production and greenhouse gas emissions from organic and inorganic fertilizer-based arable cropping systems. Agric. Ecosyst. Environ. 2010, 139, 584–594. [Google Scholar] [CrossRef]
  167. Miransari, M. Soil microbes and plant fertilization. Appl. Microbiol. Biotechnol. 2011, 92, 875–885. [Google Scholar] [CrossRef]
  168. Miskoska-Milevska, E.; Najdenovka, O.; Popovski, Z.; Imovska, D. The influence of the microbiological fertilizer–Slavol on cauliflower growth. Rom. Biotechnol. Lett. 2018, 23, 13511–13516. Available online: https://eprints.ugd.edu.mk/21862/1/Impakt%20trud.pdf (accessed on 18 January 2022).
  169. EL Boukhari, M.E.M.; Barakate, M.; Bouhia, Y.; Lyamlouli, K. Trends in Seaweed Extract Based Biostimulants: Manufacturing Process and Beneficial Effect on Soil-Plant Systems. Plants 2020, 9, 359. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  170. Nanda, S.; Kumar, G.; Hussain, S. Utilization of seaweed-based biostimulants in improving plant and soil health: Current updates and future prospective. Int. J. Environ. Sci. Technol. 2021. [Google Scholar] [CrossRef]
  171. Li, W.; Zhang, F.; Cui, G.; Wang, Y.; Yang, J.; Cheng, H.; Liu, H.; Zhang, L. Effects of bio-organic fertilizer on soil fertility, microbial community composition, and potato growth. ScienceAsia 2021, 47, 347. [Google Scholar] [CrossRef]
  172. Abhilash, P.C.; Dubey, R.K.; Tripathi, V.; Gupta, V.K.; Singh, H.B. Plant Growth-Promoting Microorganisms for Environmental Sustainability. Trends Biotechnol. 2016, 34, 847–850. [Google Scholar] [CrossRef]
  173. EC. Digestate and Compost as Fertilisers: Risk Assessment and Risk Management Options; European Commission: Bruxelles, Belgium, 2019; Available online: https://ec.europa.eu/environment/chemicals/reach/pdf/40039%20Digestate%20and%20Compost%20RMOA%20-%20Final%20report%20i2_20190208.pdf (accessed on 18 January 2022).
  174. Katada, S.; Fukuda, A.; Nakajima, C.; Suzuki, Y.; Azuma, T.; Takei, A.; Takada, H.; Okamoto, E.; Kato, T.; Tamura, Y.; et al. Aerobic Composting and Anaerobic Digestion Decrease the Copy Numbers of Antibiotic-Resistant Genes and the Levels of Lactose-Degrading Enterobacteriaceae in Dairy Farms in Hokkaido, Japan. Front. Microbiol. 2021, 12, 737420. [Google Scholar] [CrossRef] [PubMed]
Figure 1. Methodology steps.
Figure 1. Methodology steps.
Applsci 12 01198 g001
Table 1. Organic fertilizers.
Table 1. Organic fertilizers.
TypeProduction Process and MaterialsPros and ConsRefs.
Biochar and biochar-based fertilizersPyrolysis (thermal decomposition of organic matter with absence of or very limited access to oxygen), hydrothermal liquefaction and gasification of different type of biomass (agricultural residues, sewage sediment, forest waste, energy crops and residues from agro-food processing)They improve physical, chemical and biological properties of soil, together with nutrient absorption and cation exchange capacity. They reduce the uptake of metals, pesticides, PAHs, engineered nanomaterials, and pharmaceuticals by plants. The type of biomass used influences the biochar properties. If used together with other fertilizers, they can reduce their beneficial effects. [28,29,30]
Biofertilizers or microbial fertilizers (bacteria, algae, fungi or biological compounds), including-plant-growth-promoting bacteriaIsolation of microbes, screening, scale-upIncrease soil fertility by various macro- and micronutrients; improve soil biodiversity and plant growth by increasing the accessibility to or uptake of nutrients from a limited soil nutrient pool. Power of biofertilizers depends on the type of microorganism used and their metabolic activity during and after field applications.[9,10,11,31,32]
BiosolidsStabilization of organic solids from sewage treatment processes (mainly from biological treatment of wastewater). The stabilization reduces the pathogen presenceThey contain macro and micronutrients in variable quantities; K concentrations are commonly low, so that an additional K fertilization may be necessary. They can contain pathogens, traces of metals, pharmaceuticals, personal care products and other organic contaminants (e.g., phthalates, pesticides, phenols, PCBs, dioxins).[33,34]
Bio-surfactantsSurface-active biomolecules produced by microorganisms (bacteria, yeasts and fungi); they have both hydrophilic and hydrophobic regionsThey increase the surface area of hydrophobic substrates (e.g., hydrocarbon pollutants, heavy metals or nutrients) increasing their bioavailability (solubilisation/desorption). They also regulate the attachment and removal of microorganisms from surfaces. Used for hydrocarbon biodegradation in contaminated soil, for plant pathogen elimination thanks to their antifungal, antiviral, insecticidal and antimycoplasma activities and for increasing the nutrient bioavailability for beneficial plant-associated microbes.[35,36,37]
CompostComposting (biological decomposition under controlled moisture, self-heating and aerobic conditions) of animal manure, sewage sludge, municipal solid waste and green wastesSimplicity of technologies and possibility of implementation on every farm; quality protocols are provided in several countries for reducing pathogen, heavy metal and organic pollutant presence.[38,39]
Green waste or biowasteDifferent origins: crop residues, food and kitchen waste. It does not include forestry or agricultural residues, manure, sewage sludge or other biodegradable waste such as natural textiles, paper or processed wood.Improve soil structure; low nutrient content; could contain plant pathogens.[40]
DigestateAnaerobic fermentation of different organic wastes (food waste, manure and energy crops). Microorganisms, under anaerobic conditions, convert organic matter into biogas and digestateProduction of biogas; digestate could contains residual concentrations of contaminants (e.g., plastics, pharmaceuticals, including antibiotics, etc.) depending on the type of biowaste used; a duff layer could be formed on soil surface that hinders seed germination. [38,41,42,43]
Manure Mainly from beef, pig or poultry livestockImprove soil structure (depending on its origin). Increase in potentially mineralizable N. Potentially pathogenic; could contain heavy metals used for animal feed, manily Zn and Cu; could contain pharmaceutical residues and antibiotic resistance genes; water pollution by nitrates or by P in intensive livestock productions by spreading manure rich in N and P out of the soil capacity.[44,45,46,47]
VermicompostVermicomposting, a bio-oxidative process involving several organic materials (e.g., sewage sludge, crop residues, manure, digestate) using mainly epigeic earthworm species and different microorganisms.It is rich in microorganisms, nutrients, vitamins, and growth hormones; used also as biocontrol agents against diseases and pests. The nutrient-rich compost could also be used for biogas production.[48,49,50,51]
Table 2. Relevant data from the articles distributed on countries (continents) and research topics.
Table 2. Relevant data from the articles distributed on countries (continents) and research topics.
SubjectArticles Distribution by Countries (Continents)
GeneralEuropeChinaNorth AmericaOthers
Effects of chemical fertilizers on biomass, activity and diversity of soil microorganisms1722
Types of fertilizers used and their influence on soil microbial community8314
Bacterial and fungal species affected by chemical or organic fertilizers3613
Negative effects of chemical fertilizers on soil ecosystem5125
Total1817413
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Dincă, L.C.; Grenni, P.; Onet, C.; Onet, A. Fertilization and Soil Microbial Community: A Review. Appl. Sci. 2022, 12, 1198. https://doi.org/10.3390/app12031198

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Dincă LC, Grenni P, Onet C, Onet A. Fertilization and Soil Microbial Community: A Review. Applied Sciences. 2022; 12(3):1198. https://doi.org/10.3390/app12031198

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Dincă, Lucian Constantin, Paola Grenni, Cristian Onet, and Aurelia Onet. 2022. "Fertilization and Soil Microbial Community: A Review" Applied Sciences 12, no. 3: 1198. https://doi.org/10.3390/app12031198

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