Next Article in Journal
Proposing a New Approach to Generate the Differential Trajectory of the Differential Relays Using COMTRADE Files
Next Article in Special Issue
Islands of Milk Insecurity in World’s Leading Milk Producer: A Case of Andaman and Nicobar Islands, India
Previous Article in Journal
Climate Change, Food Security, and Health: Harnessing Agroecology to Build Climate-Resilient Communities
Previous Article in Special Issue
Suggesting an Extensive Interpretation of the Concept of Novelty That Looks at the Bio-Cultural Dimension of Food
 
 
Font Type:
Arial Georgia Verdana
Font Size:
Aa Aa Aa
Line Spacing:
Column Width:
Background:
Review

Sustainable Agricultural Systems for Fruit Orchards: The Influence of Plant Growth Promoting Bacteria on the Soil Biodiversity and Nutrient Management

Agriculture Research Center, Agrofood Techis, 9020-418 Funchal, Portugal
*
Author to whom correspondence should be addressed.
Sustainability 2022, 14(21), 13952; https://doi.org/10.3390/su142113952
Submission received: 2 September 2022 / Revised: 15 October 2022 / Accepted: 24 October 2022 / Published: 27 October 2022
(This article belongs to the Special Issue Sustainable Food Systems and Food Safety)

Abstract

:
Awareness towards the loss of soil quality as well as consumer perception about the environmental impact of agricultural activity have stimulated research and government activity toward the implementation of a sustainable agricultural system. The European Commission, in the next funding program, established specific objectives to promote the conversion towards a more environmentally sustainable agricultural system through its Green Deal Strategy. The demand for ecologically and sustainably cultivated fruits increases every year; however, suppressing such demand is necessary to improve the production performance of orchards. The sustainable management of orchard production requires combined knowledge from different fields. The key challenge is to design orchard systems that can integrate sustainable practices, nutrient cycle knowledge and promotion of soil biodiversity. Therefore, this review compiles works that address the challenges in the implementation of a sustainable agriculture system based on Plant Growth-Promoting Bacteria (PGPB) and their impact on soil biodiversity as well as that of nutrient management on the development of fruit orchards.

1. Introduction

Chemical inputs have driven the productivity of the agricultural sector over the final part of the last century. Such overuse has led to a theoretical limit of agrochemical efficiency, a point from which further application does not directly correspond to further crop yield increments [1].
The pursuit for boosting agricultural yields, to supplement ever-increasing food demand from a rising human population, had progressed to an imbalanced application of agrochemicals to overcome the reduced crop production at higher costs. As a consequence, production costs increased to overcome the reduced crop yield as well as alterations of soil properties, such as its physical, chemical and biodiversity characteristics. The progress of these alterations could disrupt fundamental services provided by the soil ecosystem, such as the water cycle, nutrient cycle, or climate regulation [2]. To overcome the rising environmental and climate problems, there is an incremental effort to develop efficient solutions in all economic activities, including agriculture. Awareness of soil ecosystem importance and associated problems has increased since the beginning of the XXI century (2002) through several initiatives from the Food and Agriculture Organization (FAO) and the United Nations (UN), such as the International Initiative for the Conservation and Sustainable Use of Soil Biodiversity. The peak of such campaigns was achieved with the declaration of the United Nations Decade on Ecosystem Restoration (2021–2030) and the release of the UN–FAO report, the State of Knowledge of Soil Biodiversity [3,4].
In the case of the European Union (EU), similar concerns have been part of agricultural policies for example, the Common Agricultural Policy (CAP) and investment initiatives programs (e.g., Horizon 2020) [5]. More recently, to overcome climate challenges, as well as to protect and improve natural capital and citizens’ health, the EU has released its plan to improve sustainability in all economic sectors: the European Green Deal Strategy. At the center of the plan is the Farm to Fork strategy and Biodiversity Policy for 2030, where the need is emphasized to improve the balance between biodiversity and food systems to increase competitiveness and resilience [6]. Implementing the European Green Deal strategy will generate challenges and opportunities. Even though strategies of appropriate production practices and sustainability programs have been in place for years, large-scale adoption is still lacking. Beliefs about the high costs of sustainable approaches over the expected return in the medium and long term, as well as the lack of knowledge of some producers about the correct implementation of such approaches, could hinder the Green Deal’s implementation [6,7].
The objective of this work is to review information on the state of sustainable management approaches for the implementation of sustainable agriculture systems based on Plant Growth-Promoting Bacteria (PGPB), and their impact on soil biodiversity and nutrient management on fruit orchard development, addressing innovative practices, nutritional management and soil biodiversity protection.

2. Sustainability Concept

Sustainability definition is a difficult endeavor due to the need to reflect and integrate multiple goals, values and priorities that shift over time. Difficulty in defining it is also one of the reasons for discord and ineffective implementation. However, the current perception of the sustainability concept is based on three pillars: economic, environmental and social. Even though other dimensions are commonly considered (e.g., institutional, political, and ethical), it is recognized that they are interdependent and interlinked, as shown in Figure 1 [8,9].
Trigo et al. (2021), identified in the literature two main interpretations of sustainable agriculture. One is described as a philosophical base, focused on the goal of embracing alternative methods to diminish the impact of agricultural activities, with the distortion of circular perspective and no clear approved alternative. The other approach is sustained by a set of goal-oriented strategies, based on scientific knowledge, practices, technologies, or policies (e.g., mimic nature, regenerative and circular approach) [9]. This last conceptualization is the base of the future vision stated in the 2030 Agenda for Sustainable Development, in which concern for the environment occupies a central role [9].
Sustainable food production in agriculture is an extensive process based on alternative approaches to industrial agriculture management, which depend on the increment of production yields using agrochemicals for nutrient inputs and pest controls. Sustainable agriculture is supported by new technical developments and management, highlining the need for more attention on environmental protection [8]. The main objective is to fulfill food human requirements, reducing the negative burden on the environment and its resources through management of soil fertility and its physical–chemical properties, using a regenerative approach, while improving or maintaining economic viability [10,11]. Therefore, for an efficient implementation of a sustainable food system and the establishment of specific targets, evaluation parameters, and proper assessment tools are necessary to sustain further policy changes, and support the transition to sustainable practices.
The following chapters will be discussed some topics for a sustainable agriculture system. Specific attention will be given to the nutrient cycle, sustainable management practices, and the impact of biodiversity on the soil.

3. Sustainable Agriculture Systems

Terrestrial ecosystems have as their basis the natural complex dynamic of soil structures. Its biological (e.g., soil biodiversity), chemical (e.g., nutrients cycle), and physical properties (e.g., bulk density, porosity) are important prerequisites to support plant growth. Awareness of the interactions between all properties in an ecological cycle is the basis of sustainable agriculture. Therefore, indices of soil health should integrate the examination of all soil properties essentially to achieve an understanding of soil quality [1].
Sustainable principles are of utmost importance when applied to orchards, since they also have interesting features for a balanced ecosystem service; for example, the contribution of biodiversity, the impact of carbon sequestration, or water regulation [12].

3.1. Sustainable Practices

Sustainable practices are a set of medium- and long-term strategies based on ecological cycles to maintain soil functions and services, as well to provide economic crop production and ecological protection. Nevertheless, the sustainability of the system is more dependent on the choice of management practices other than the farming structure. Alternative practices generally diverge from conventional operations, in the intensity and quantity of soil manipulations as well the nature of nutritional inputs (e.g., large volumes of agrochemicals nutrients vs. organic amendments) [13,14]. Table 1 represents some of the most utilized management practices and sustainable systems. The described approaches also contribute to pest management. Sustainable pest management and weed control are linked with cropping techniques (e.g., rotation, seeding timing, or flaming), biological control and natural pesticides (e.g., plant extracts).
Several studies have evaluated the efficiency of sustainable management practices as the pros and constraints of such practices [15,16,17,18,19]. The antagonism between the conventional and sustainable approaches is centered on maximizing economic growth, protecting the environment and providing adequate metrics for evaluation to support evidence of the unsustainability of industrial agriculture and that alternative approaches can achieve adequate yields [20]. On the encouraging side, organic tactics serve higher ecological outcomes, improve soil quality, increase profitability, and present higher nutritional value. On the adverse side are higher costs and prices and lower yields [16]. Furthermore, other factors that influence the adoption of or enrollment in sustainable practices by the farmers were reviewed by Liu et al. (2018) [21]. According to Liu et al., the farmers’ knowledge is acquired as a temporally dynamic learning process, divided into four stages: (1) awareness—they become conscious about the alternative approaches and potential relevance to them. (2) Interest—collection of information about the practices. (3) Trial and evaluation—application on smaller portions of terrain, evaluation of the results and skills development. (4) Adoption and adaptation—the decision to scale up and customize practices in the fields. Among the main attributes that influence this process are farmers’ characteristics (e.g., age, experience, education, heritage, “lifestyle” and environmental consciousness), farm traits (e.g., size, soils, land tenure, type of production) and financial motivation (government subsidies, farm income and off-farm income). Other uncertain associated factors are related to peer pressure, social norms, geographic regions, policies and markets [21].

3.2. Nutritional Management

Nutrient management considers the estimation of nutrient budgets. This means integrating knowledge about the soil’s nutrient capacity and crop nutrient needs and quantifying the amount of nutrients present in inputs (e.g., manure) to avoid the application of disproportionate nutrient concentrations to the plants and soil. In the case of orchards, nutrient application should be performed cautiously before and after harvest [22]. Nutrients are biochemical elements with organic or synthetic origins that are used by plants and other organisms for their development. For fruit orchards, such nutrients also have a significant role in fruit development [23], nutritional value [24] and pest control [25].
Nutrient deficiency may result in decreased plant quality and/or productivity. It also can induce an imbalance of overall biodiversity since plants reinforce above-ground and below-ground food webs. In addition, appropriate nutrient concentration up to the tolerance levels stimulates the absorption of other nutrients (synergism). The occurrence of excess levels of a particular nutrient may inhibit the accumulation of others (antagonism). Therefore, is necessary to improve plant nutrient efficiency, which requires knowledge about how they are used by the plant considering the development stage of the plant/tree and species specificity [26].
The nutrient cycle refers to the transformation of compounds from the original bedrock and soil organic matter decomposition (SOM), into simple molecules that are assimilable by several organisms and plants. SOM is a complex element of soil because it consists of several carbon sources (e.g., plant, microbial, and animal bodies) in diverse disintegration stages and provides a mixture of heterogeneous macro and micro, organic and inorganic constituents. Therefore, it is an integrated part of the nutrients cycle, with benefic effects on soil properties and consequently on plant development [27]. Factors that influence the nutrients availability and accessibility for plants uptake are climate (e.g., temperature), soil physical properties (e.g., texture, structure, moisture), and chemical parameters (e.g., pH, SOM). Furthermore, nutrient use efficiency is influenced by cover plant chemical composition, as well as the taxonomic and functional diversity of soil biodiversity (e.g., microorganisms) [4]. The soil nutrient pool includes macronutrients as well as micronutrients. The macronutrients are constantly referred to as the most important in any crop or orchard system, due to their impact on plant growth and production. They are represented by nitrogen (N) [28,29], potassium (K) [30,31] and phosphorus (P) [32]. Others that are required but possess a secondary degree of importance are calcium [33], magnesium and sulfur [34]. Table 2 summarizes the impact of the main macronutrients on plants. Micronutrients, for example iron (Fe) or boron (B), are required as cofactors for enzyme activity, and other biological functions as summarized in Table 3.
Knowledge about the nutritional needs of plants is important for an efficient administration not only of the nutrients but also of the adopted management practices. The analysis of plant nutritional status can be achieved by four different approaches: (i) foliar symptoms; (ii) plant tissues analysis; (iii) soil analysis; (iv) biological tests of higher plants or microorganisms. None of the previous approaches should be taken as the optimal method, but should be considered as supplements to each other. Table 4 presents the leaf nutritional requirements in different fruit orchards. The nutritional deficit may be caused by more than one nutrient or be driven by the excessive quantity of other nutrients. In addition, damage originating from disease, herbicide or insects can cause similar symptoms to macronutrient or micronutrient deficiency or excess. Therefore, the inclusion of soil and water analysis should be included to assist in proper management decisions [35].

3.3. Plant Growth Promoting Bacteria (PGPB)

The biological diversity of soil is important to regulate the nutrients cycle and physical properties of the soil, which also influence the provided ecosystem services (e.g., nutrient cycle, water-holding, CO2 sequestration) [52]. The soil is a complex and heterogeneous system, comprising organo-mineral aggregates of different sizes and organic components that create habitats for soil biodiversity across multiple spatial scales; the diversity in habitat composition with pores of different sizes filled with air and/or water allows an incredible number of taxa of different sizes and ecology to inhabit it. Soils are one of the main reservoirs of biodiversity, arranged in a complex heterogeneous system. They can be characterized by size fraction and functional importance [4].
Microbes with a size range of 20 nm to 10 μm (e.g., virus, bacteria, Archaea, fungi) and Microfauna 10 μm to 0.1 mm (e.g., soil protozoa and nematodes) inhabit soil. Their main functional activity encompasses the decomposition of soil organic matter into several macronutrients and micronutrients [53]. Mesofauna range in size between 0.1–2 mm and encompass microarthropods (e.g., mites). They boost the soil’s active biochemical interactions, participating in litter transformation/fragmentation, creating new surfaces for microbial attack [4]. Macrofauna, from 2–20 mm, include large invertebrates (e.g., earthworms). They actively participate in litter transformation and predation, while some are plant herbivores or modify soil structure, improving the energy and nutrient flux [54]. Megafauna (>20 mm) are vertebrates (e.g., Mammalia, reptilians and amphibia). They generate soil spatial heterogeneity as alterations in its profile through movement [4]. As a resume, Figure 2 represents the integration of the interactions between PGPB, soil characteristics; plants/tree mechanisms and biodiversity, to plant sustainability [11,24,55].
Among the described taxa, microorganisms have been gathering increasing interest and efforts in scientific works as biofertilizers. They have been recognized as an important influence on nutrient accessibility, uptake efficiency, and the ability to recover soil health and status. Biofertilizers are agricultural supplements that contain live or dormant microorganisms that assist the overall plant growth and yield increments in an eco-friendly way. The main constituent of biofertilizers is root-colonizing bacteria thriving in the plant rhizosphere and bulk soil. They are frequently denominated as Plant growth-promoting bacteria (PGPB). They are common facilitators of plant accessibility to nutrients, and endurance facing biotic and abiotic stresses [10,56].
Most of the PGPB are found in the plant rhizosphere, which is a constricted zone of soil contiguous to the plant root system. This zone, which displays essential ecological functions is colonized by prokaryotes (e.g., archaea, and viruses) and eukaryotes (e.g., fungi, algae). All of the present taxa are potential biofertilizers or important constituents of plant biostimulants [57]. The rhizosphere-specific ecosystem is supported by the synergetic effect of root exudates (e.g., carbohydrates lipids, or amino acids) and soil properties (e.g., pH, bulk density, aeration or water-holding), which directly or indirectly assist in growth promotion and stress management.
The most common bacterial strains used and studied as biofertilizers or soil amendments are: Bacillus sp.; Agrobacterium sp.; Pseudomonas sp.; Arthrobacter sp.; Streptomyces sp.; Sinorhizobium sp.; Serratia sp.; Azospirillum sp.; etc. Table 5 shows some recent studies, with applications of PGPB in different fruit orchards. The most common fields of study are disease tolerance, growth performance, fruit yield and nutrient uptake. The interactions between PGPB and plants rhizomes are commonly divided into two mechanisms, direct and indirect processes, that have been the target of several reviews [25,56,58,59,60,61]. Direct mechanisms encompass the processes that have a direct influence on plant performance, among which are: Biological nitrogen fixation; Mineral solubilization/mobilization (e.g., K, P, Zn); and plant growth regulators (e.g., auxin or gibberellin). Indirect mechanisms are related to antagonist activity against pests and pathogens. It also comprises the formation of volatile organic compounds, antibiotics, or biosurfactants, induced systemic resistance, and stress tolerance [25,56,58,59,60,61].
In Table 5, specific examples of the application of PGPB in fruit orchards can be found, for different species. In the case of apples according to Kuzin et al., 2020, fruit yield (kg tr−1), was improved when PGPB was applied (12–13%), in comparison with the control (11%) [62]. Thokchom et al., 2014, applied PGPB to citrus plant and evaluated the growth, registering an increase on plant height (40–55 cm) when compared with the control (31 cm) [90]. Another area of investigation is disease tolerance, as studied by Ali et al., 2022. In this work the application of PGPB reduced necrosis symptoms caused by PSA (Pseudomonas syringae pv. actinidiae) in 92% of kiwi leaves after 10 days [82]. Gani et al., 2021, studied PGPB’s effect on pesticide stress tolerance on peach, detecting the degradation of different concentrations of chlorpyrifos within 30 days, accompanied by the increased production of antioxidants and exopolysaccharides [75]. These examples demonstrate the capability of PGPB when applied in fruit orchards, with promising results.
However, the development of new bio inoculants, their large-scale production and field application have to address specific PGPB characteristics and overcome several operational constraints to improve its efficiency and effectivity (Figure 3). The mere use of primary screening strategies to obtain culture isolates for PGPB traits could result in isolates that perform well in the laboratorial environment but may not be efficient under field application. On the other hand, the discarded colonies might possess different strategies, more suitable to a specific environment due to different mechanisms of action, and be rejected. This might occur because they are not recognized by the standard screening conditions, which might not be suitable to recognize such different approaches. In the case of operational constraints, they consist mostly of required investment, the equipment needed and essential know-how to achieve the mandatory product quality and performance [2,96].

4. Future Prospects

Ecological innovation triggered by chemical or physical engineering is achieving its maximum development, not only because of resource over-supplementation, but also due to the practical hurdles, difficulties in crop yield improvement and economic challenges. The continuous use of conventional farming practices might not be sufficient to achieve the necessary yields from crops and orchards needed to feed the ever-growing human population. To alter such a situation, it is necessary to readdress attention to soil health and to the services provided by the ecosystem, as means to accomplish the sustainable development of agricultural practices. For that, a change of agricultural paradigm, to a system based on soil-plant–bacterial interactions, is necessary to restore soil health and quality [71].
It will also be necessary to bridge the knowledge from basic, applied research and field experience, to achieve a fundamental understanding of the complex interactions between soil, plants and PGPB. The present knowledge perspective indicates the use of microorganisms as soil inoculants and eco-friendly fertilizer, to improve soil quality and plant efficiency. However, microorganisms are more effective when adequate conditions are provided, to achieve maximum metabolic efficiency (e.g., water, pH, oxygen, or temperature). Future advances on the knowledge of mechanisms of PGPB action will open new windows to project strategies to increment biofertilizer efficiency [14].
In the specific case of sustainable orchard systems, further knowledge is necessary on plant nutrient dynamics (e.g., carryover effects from remobilization) as well on soil and root dynamics to provide new management techniques, enhance fruit quality and productivity. The development of specific rootstocks and tree species suitable for sustainable systems is required [36].
Another important field of action is the discussion of proposals and public policies to promote the conversion to sustainable management practices to support the costs and hurdles of the transition from conventional agriculture [21].
Simultaneous and concerted efforts between the previously described topics are a requirement for well-established integrated soil management practice. Besides such integrated visions still being in their first steps, they has the potential to transform actual sustainable practices into a much more efficient system in terms of biodiversity protection and the production of sustainable agriculture systems for fruit orchards.

Author Contributions

Conceptualization, P.S. and J.F.; formal analysis, P.S. and J.F.; investigation, P.S. and J.F.; resources, P.S. and J.F.; data curation, P.S. and J.F.; writing—original draft preparation, J.F.; writing—review and editing, P.S. and J.F.; visualization, P.S. and J.F.; supervision, P.S.; project administration, P.S.; funding acquisition, P.S. All authors have read and agreed to the published version of the manuscript.

Funding

This research was funded by Instituto de Desenvolvimento Empresarial, IP-RAM, by the Programa Operacional “Madeira 14–20”, (co-funded in 85%, by Fundo Europeu de Desenvolvimento Regional (FEDER) and 15% by Autonomous Region of Madeira Government Budget), in Priority Axis 1—“Reinforce Research, Technological Development and Innovation”, which includes Investment Priority 1. b—“Promotion of investment by companies in innovation and research, the development of links and synergies between companies, Research and Development (R&D) Centers”, through application M1420-01-0247-FEDER-000046 submitted to the Incentive System for the Production of Scientific Knowledge and Technology of the Autonomous Region of Madeira—PROCiência 2020, by the company “AGROFOOD TECHIS, UNIPESSOAL LDA”, legal person and single registration nº 515777234.

Institutional Review Board Statement

Not applicable.

Informed Consent Statement

Not applicable.

Acknowledgments

The authors acknowledge the Instituto de Desenvolvimento Empresarial, IP-RAM, and the AGROFOOD TECHIS, UNIPESSOAL LDA, through the support granted under the application M1420-01-0247-FEDER-000046—PROCiência 2020.

Conflicts of Interest

The authors declare no conflict of interest.

References

  1. Aeron, A.; Khare, E.; Jha, C.K.; Meena, V.S.; Aziz, S.M.A.; Islam, M.T.; Kim, K.; Meena, S.K.; Pattanayak, A.; Rajashekara, H.; et al. Revisiting the plant growth-promoting rhizobacteria: Lessons from the past and objectives for the future. Arch. Microbiol. 2020, 202, 665–676. [Google Scholar] [CrossRef] [PubMed]
  2. Basu, A.; Prasad, P.; Das, S.N.; Kalam, S.; Sayyed, R.Z.; Reddy, M.S.; Enshasy, H. El Plant Growth Promoting Rhizobacteria (PGPR) as Green Bioinoculants: Recent Developments, Constraints, and Prospects. Sustainability 2021, 13, 1140. [Google Scholar] [CrossRef]
  3. Geisen, S.; Hartmann, M.; Tebbe, C.C. The European Journal of Soil Biology: A catalyst for soil biodiversity research. Eur. J. Soil Biol. 2021, 102, 103262. [Google Scholar] [CrossRef]
  4. FAO; ITPS; GSBI; CBD; EC. State of Knowledge of Soil Biodiversity—Status, Challenges and Potentialities; FAO: Rome, Italy, 2020. [Google Scholar]
  5. Herencia, J.F.; Pérez-Romero, L.F.; Daza, A.; Arroyo, F.T. Chemical and biological indicators of soil quality in organic and conventional Japanese plum orchards. Biol. Agric. Hortic. 2021, 37, 71–90. [Google Scholar] [CrossRef]
  6. Dobbs, M.; Gravey, V.; Petetin, L. Driving the european green deal in turbulent times. Polit. Gov. 2021, 9, 316–326. [Google Scholar] [CrossRef]
  7. Prandecki, K.; Wrzaszcz, W.; Zieliński, M. Environmental and climate challenges to agriculture in poland in the context of objectives adopted in the european green deal strategy. Sustainability 2021, 13, 10318. [Google Scholar] [CrossRef]
  8. McNeill, D. The Contested Discourse of Sustainable Agriculture. Glob. Policy 2019, 10, 16–27. [Google Scholar] [CrossRef] [Green Version]
  9. Trigo, A.; Marta-Costa, A.; Fragoso, R. Principles of sustainable agriculture: Defining standardized reference points. Sustainability 2021, 13, 4086. [Google Scholar] [CrossRef]
  10. Dilnashin, H.; Birla, H.; Hoat, T.X.; Singh, H.B.; Singh, S.P.; Keswani, C. Applications of agriculturally important microorganisms for sustainable crop production. In Molecular Aspects of Plant Beneficial Microbes in Agriculture; INC: New York, NY, USA, 2020; pp. 403–415. ISBN 9780128184691. [Google Scholar]
  11. Singh, M.; Singh, D.; Gupta, A.; Pandey, K.D.; Singh, P.K.; Kumar, A. Plant Growth Promoting Rhizobacteria; Elsevier Inc.: Amsterdam, The Netherlands, 2019; ISBN 9780128158791. [Google Scholar]
  12. Demestihas, C.; Plénet, D.; Génard, M.; Raynal, C.; Lescourret, F. Ecosystem services in orchards. A review. Agron. Sustain. Dev. 2017, 37, 12. [Google Scholar] [CrossRef]
  13. Gomiero, T.; Pimentel, D.; Paoletti, M.G. Environmental Impact of Different Agricultural Management Practices: Conventional vs. Organic Agriculture. Crit. Rev. Plant Sci. 2011, 30, 95–124. [Google Scholar] [CrossRef]
  14. Norris, C.; Congreves, K.A. Alternative Management Practices Improve Soil Health Indices in Intensive Vegetable Cropping Systems: A Review. Front. Environ. Sci. 2018, 6, 50. [Google Scholar] [CrossRef]
  15. Rosa-Schleich, J.; Loos, J.; Mußhoff, O.; Tscharntke, T. Ecological-economic trade-offs of Diversified Farming Systems—A review. Ecol. Econ. 2019, 160, 251–263. [Google Scholar] [CrossRef]
  16. Fess, T.L.; Benedito, V.A. Organic versus conventional cropping sustainability: A comparative system analysis. Sustainability 2018, 10, 272. [Google Scholar] [CrossRef] [Green Version]
  17. Bai, Z.; Caspari, T.; Gonzalez, M.R.; Batjes, N.H.; Mäder, P.; Bünemann, E.K.; de Goede, R.; Brussaard, L.; Xu, M.; Ferreira, C.S.S.; et al. Effects of agricultural management practices on soil quality: A review of long-term experiments for Europe and China. Agric. Ecosyst. Environ. 2018, 265, 1–7. [Google Scholar] [CrossRef]
  18. Yadav, S.K.; Babu, S.; Yadav, M.K.; Singh, K.; Yadav, G.S.; Pal, S. A Review of Organic Farming for Sustainable Agriculture in Northern India. Int. J. Agron. 2013, 2013, 1–8. [Google Scholar] [CrossRef] [Green Version]
  19. Seufert, V.; Ramankutty, N. Many shades of gray—The context-dependent performance of organic agriculture. Sci. Adv. 2017, 3, e1602638. [Google Scholar] [CrossRef] [Green Version]
  20. Röös, E.; Mie, A.; Wivstad, M.; Salomon, E.; Johansson, B.; Gunnarsson, S.; Wallenbeck, A.; Hoffmann, R.; Nilsson, U.; Sundberg, C.; et al. Risks and opportunities of increasing yields in organic farming. A review. Agron. Sustain. Dev. 2018, 38, 1–21. [Google Scholar] [CrossRef] [Green Version]
  21. Liu, T.; Bruins, R.J.F.; Heberling, M.T. Factors influencing farmers’ adoption of best management practices: A review and synthesis. Sustainability 2018, 10, 432. [Google Scholar] [CrossRef] [Green Version]
  22. Mir, M.M.; Iqbal, U.; Mir, S.A. Proudction Technology of Stone Fruits; Springer Nature Singapore Pte Ltd.: Singapore, 2021; ISBN 9789811589195. [Google Scholar]
  23. Bustamante, M.; Muñoz, A.; Romero, I.; Osorio, P.; Mánquez, S.; Arriola, R.; Reyes-Díaz, M.; Ribera-Fonseca, A. Impact of potassium pre-harvest applications on fruit quality and condition of sweet cherry (Prunus avium L.) cultivated under plastic covers in southern chile orchards. Plants 2021, 10, 2778. [Google Scholar] [CrossRef]
  24. Jiménez-Gómez, A.; Celador-Lera, L.; Fradejas-Bayón, M.; Rivas, R. Plant probiotic bacteria enhance the quality of fruit and horticultural crops. AIMS Microbiol. 2017, 3, 483–501. [Google Scholar] [CrossRef]
  25. Backer, R.; Rokem, J.S.; Ilangumaran, G.; Lamont, J.; Praslickova, D.; Ricci, E.; Subramanian, S.; Smith, D.L. Plant growth-promoting rhizobacteria: Context, mechanisms of action, and roadmap to commercialization of biostimulants for sustainable agriculture. Front. Plant Sci. 2018, 871, 1–17. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  26. Srivastava, A.K.; Malhotra, S.K. Nutrient use efficiency in perennial fruit crops—A review. J. Plant Nutr. 2017, 40, 1928–1953. [Google Scholar] [CrossRef]
  27. Ramesh, T.; Bolan, N.S.; Kirkham, M.B.; Wijesekara, H.; Kanchikerimath, M.; Rao, C.S.; Sandeep, S.; Rinklebe, J.; Ok, Y.S.; Choudhury, B.U.; et al. Soil organic carbon dynamics: Impact of land use changes and management practices: A review. Adv. Agron. 2019, 156, 1–107. [Google Scholar] [CrossRef]
  28. Cui, M.; Zeng, L.; Qin, W.; Feng, J. Measures for reducing nitrate leaching in orchards: A review. Environ. Pollut. 2020, 263, 114553. [Google Scholar] [CrossRef] [PubMed]
  29. Carranca, C.; Brunetto, G.; Tagliavini, M. Nitrogen nutrition of fruit trees to reconcile productivity and environmental concerns. Plants 2018, 7, 4. [Google Scholar] [CrossRef] [Green Version]
  30. Andrews, E.; Kassama, S.; Smith, E.; Brown, P.; Khalsa, S. A Review of Potassium-Rich Crop Residues Used as Organic Matter Amendments in Tree Crop Agroecosystems. Agriculture 2021, 11, 580. [Google Scholar] [CrossRef]
  31. Kuzin, A.; Solovchenko, A. Essential Role of Potassium in Apple and Its Implications for Management of Orchard Fertilization. Plants 2021, 10, 2624. [Google Scholar] [CrossRef]
  32. Lima, A.P.; Lourenzi, C.R.; Comin, J.J.; Loss, A.; Brunetto, G.; Souza, M.; Ventura, B.S.; Trapp, T.; Ferreira, G.W. Soil phosphorus fractions in an apple orchard with different weed managements. Res. Soc. Dev. 2020, 9, e3449108767. [Google Scholar] [CrossRef]
  33. Gulbagca, F.; Burhan, H.; Elmusa, F.; Sen, F. Calcium nutrition in fruit crops: Agronomic and physiological implications. In Fruit Crops: Diagnosis and Management of Nutrient Constraints; Elsevier Inc.: Amsterdam, The Netherlands, 2019; pp. 173–190. ISBN 9780128187326. [Google Scholar]
  34. de Bang, T.C.; Husted, S.; Laursen, K.H.; Persson, D.P.; Schjoerring, J.K. The molecular–physiological functions of mineral macronutrients and their consequences for deficiency symptoms in plants. New Phytol. 2021, 229, 2446–2469. [Google Scholar] [CrossRef]
  35. Hu, C.; Dong, Z.; Zhao, Y.; Jia, W.; Cai, M.; Zhan, T.; Tan, Q.; Li, J. Floral analysis in fruit crops: A potential tool for nutrient constraints diagnosis. In Fruit Crops: Diagnosis and Management of Nutrient Constraints; Elsevier Inc.: Amsterdam, The Netherlands, 2019; pp. 157–172. ISBN 9780128187326. [Google Scholar]
  36. Kalcsits, L.; Lotze, E.; Tagliavini, M.; Hannam, K.D.; Mimmo, T.; Neilsen, D.; Neilsen, G.; Atkinson, D.; Biasuz, E.C.; Borruso, L.; et al. Recent achievements and new research opportunities for optimizing macronutrient availability, acquisition, and distribution for perennial fruit crops. Agronomy 2020, 10, 1738. [Google Scholar] [CrossRef]
  37. Mosa, W.F.A.E.-G.; Paszt, L.S.; Frąc, M.; Trzciński, P. The Role of Biofertilization in Improving Apple Productivity―A Review. Adv. Microbiol. 2015, 05, 21–27. [Google Scholar] [CrossRef] [Green Version]
  38. Maathuis, F.J. Physiological functions of mineral macronutrients. Curr. Opin. Plant Biol. 2009, 12, 250–258. [Google Scholar] [CrossRef] [PubMed]
  39. Tipathi, D.K.; Singh, V.P.; Chauhan, D.K.; Prasad, S.M.; Dubey, N.K. Role of Macronutrients in Plant Growth and Acclimation: Recent Advances and Future Prospective. In Improvement of Crops in the Era of Climatic Changes; Springer: New York, NY, USA, 2014; Volume 2, pp. 1–368. ISBN 9781461488248. [Google Scholar]
  40. Shahrokh, V.; Khademi, H.; Faz Cano, A.; Acosta, J.A. Different forms of soil potassium and clay mineralogy as influenced by the lemon tree rhizospheric environment. Int. J. Environ. Sci. Technol. 2019, 16, 3979–3988. [Google Scholar] [CrossRef]
  41. Jat, R.K.; Kumar, M.; Jat, M.L.; Shivran, J.S. A Review on Use of Micronutrients in Tropical and Subtropical Fruit Crops. Int. J. Curr. Microbiol. Appl. Sci. 2020, 9, 2744–2753. [Google Scholar] [CrossRef]
  42. Shahane, A.A.; Shivay, Y.S. Agronomic Biofortification of Crops: Current Research Status and Future Needs. Indian J. Fertil. 2022, 18, 164–179. [Google Scholar]
  43. Alejandro, S.; Höller, S.; Meier, B.; Peiter, E. Manganese in Plants: From Acquisition to Subcellular Allocation. Front. Plant Sci. 2020, 11, 300. [Google Scholar] [CrossRef] [Green Version]
  44. Ballabio, C.; Panagos, P.; Lugato, E.; Huang, J.H.; Orgiazzi, A.; Jones, A.; Fernández-Ugalde, O.; Borrelli, P.; Montanarella, L. Copper distribution in European topsoils: An assessment based on LUCAS soil survey. Sci. Total Environ. 2018, 636, 282–298. [Google Scholar] [CrossRef]
  45. Kumar, R.; Kumar, V. Physiological disorders in perennial woody tropical and subtropical fruit crops: A review. Indian J. Agric. Sci. 2016, 86, 703–717. [Google Scholar]
  46. Zia, M.H.; Ahmad, R.; Khaliq, I.; Ahmad, A.; Irshad, M. Micronutrients status and management in orchards soils: Applied aspects. Soil Environ. 2006, 25, 6–16. [Google Scholar]
  47. Wang, N.; He, H.; Lacroix, C.; Morris, C.; Liu, Z.; Ma, F. Soil fertility, leaf nutrients and their relationship in kiwifruit orchards of China’s central Shaanxi province. Soil Sci. Plant Nutr. 2019, 65, 369–376. [Google Scholar] [CrossRef]
  48. Bright, J. Apple and pear nutrition. NSW Dep. Prim. Ind. Primefact 2005, 85, 1–12. [Google Scholar]
  49. Stiles, W.C.; Hoying, S.; Fargione, M.; Stiles, W.C. Soil Analysis and Interpretation Interpretation. N. Y. Fruit Q. 2004, 12, 1. [Google Scholar]
  50. Milošević, T.; Milošević, N. Soil fertility: Plant nutrition vis-à-vis fruit yield and quality of stone fruits. In Fruit Crops: Diagnosis and Management of Nutrient Constraints, 1st ed.; Srivastava, A.K., Hu, C., Eds.; Elsevier: Amsterdam, The Netherlands, 2019; pp. 583–606. [Google Scholar] [CrossRef]
  51. Chater, J.M.; Merhaut, D.J.; Preece, J.E. Diagnosis and management of nutrient constraints in pomegranate. In Fruit Crops: Diagnosis and Management of Nutrient Constraints; Elsevier Inc.: Amsterdam, The Netherlands, 2019; pp. 681–691. ISBN 9780128187326. [Google Scholar]
  52. Lal, R. Soil conservation and ecosystem services. Int. Soil Water Conserv. Res. 2014, 2, 36–47. [Google Scholar] [CrossRef] [Green Version]
  53. Tahat, M.M.; Alananbeh, K.M.; Othman, Y.A.; Leskovar, D.I. Soil health and sustainable agriculture. Sustainability 2020, 12, 4859. [Google Scholar] [CrossRef]
  54. Sofo, A.; Mininni, A.N.; Ricciuti, P. Soil macrofauna: A key factor for increasing soil fertility and promoting sustainable soil use in fruit orchard agrosystems. Agronomy 2020, 10, 456. [Google Scholar] [CrossRef] [Green Version]
  55. Pii, Y.; Mimmo, T.; Tomasi, N.; Terzano, R.; Cesco, S.; Crecchio, C. Microbial interactions in the rhizosphere: Beneficial influences of plant growth-promoting rhizobacteria on nutrient acquisition process. A review. Biol. Fertil. Soils 2015, 51, 403–415. [Google Scholar] [CrossRef]
  56. Meena, V.S.; Meena, S.K.; Verma, J.P.; Kumar, A.; Aeron, A.; Mishra, P.K.; Bisht, J.K.; Pattanayak, A.; Naveed, M.; Dotaniya, M.L. Plant beneficial rhizospheric microorganism (PBRM) strategies to improve nutrients use efficiency: A review. Ecol. Eng. 2017, 107, 8–32. [Google Scholar] [CrossRef]
  57. Pylak, M.; Oszust, K.; Frąc, M. Review report on the role of bioproducts, biopreparations, biostimulants and microbial inoculants in organic production of fruit. Rev. Environ. Sci. Biotechnol. 2019, 18, 597–616. [Google Scholar] [CrossRef] [Green Version]
  58. Orozco-Mosqueda, M.; del, C.; Flores, A.; Rojas-Sánchez, B.; Urtis-Flores, C.A.; Morales-Cedeño, L.R.; Valencia-Marin, M.F.; Chávez-Avila, S.; Rojas-Solis, D.; Santoyo, G. Plant growth-promoting bacteria as bioinoculants: Attributes and challenges for sustainable crop improvement. Agronomy 2021, 11, 1167. [Google Scholar] [CrossRef]
  59. Goswami, D.; Thakker, J.N.; Dhandhukia, P.C. Portraying mechanics of plant growth promoting rhizobacteria (PGPR): A review. Cogent Food Agric. 2016, 2, 1127500. [Google Scholar] [CrossRef]
  60. Singh, I. Plant Growth Promoting Rhizobacteria (PGPR) and their various mechanisms for plant growth enhancement in stressful conditions: A review. Eur. J. Biol. Res. 2018, 8, 191–213. [Google Scholar] [CrossRef]
  61. Bhattacharyya, P.N.; Jha, D.K. Plant growth-promoting rhizobacteria (PGPR): Emergence in agriculture. World J. Microbiol. Biotechnol. 2012, 28, 1327–1350. [Google Scholar] [CrossRef]
  62. Kuzin, A.; Solovchenko, A.; Stepantsova, L.; Pugachev, G. Soil fertility management in apple orchard with microbial biofertilizers. In Proceedings of the E3S Web of Conferences, Constanta, Romania, 26–27 June 2020; Volume 222. [Google Scholar]
  63. Aslantaş, R.; Çakmakçi, R.; Şahin, F. Effect of plant growth promoting rhizobacteria on young apple tree growth and fruit yield under orchard conditions. Sci. Hortic. 2007, 111, 371–377. [Google Scholar] [CrossRef]
  64. Pirlak, L.; Turan, M.; Sahin, F.; Esitken, A. Floral and foliar application of Plant Growth Promoting Rhizobacteria (PGPR) to apples increases yield, growth, and nutrient element contents of leaves. J. Sustain. Agric. 2007, 30, 145–155. [Google Scholar] [CrossRef]
  65. Aras, S.; Arıkan, Ş.; Ipek, M.; Eşitken, A.; Pırlak, L.; Dönmez, M.F.; Turan, M. Plant growth promoting rhizobacteria enhanced leaf organic acids, FC-R activity and Fe nutrition of apple under lime soil conditions. Acta Physiol. Plant. 2018, 40, 120. [Google Scholar] [CrossRef]
  66. Li, B.; Zhang, C.; Qi, M.; Mustafad, N.S.; Ahmed, N.; Anees, M.; Ahanger, M.A.; Zhang, L. Effects of plant growth-promoting rhizobacteria on uptake and utilization of phosphorus and root architecture in apple seedlings under water limited regimes Plant material. Int. J. Appl. Exp. Biol. 2022, 1, 1–8. [Google Scholar] [CrossRef]
  67. Treder, W.; Klamkowski, K.; Wójcik, K.; Tryngiel-Gać, A.; Sas-Paszt, L.; Mika, A.; Kowalczyk, W. Apple leaf macro- and micronutrient content as affected by soil treatments with fertilizers and microorganisms. Sci. Hortic. 2022, 297, 110975. [Google Scholar] [CrossRef]
  68. Duan, Y.; Zhou, Y.; Li, Z.; Chen, X.; Yin, C.; Mao, Z. Effects of Bacillus amyloliquefaciens QSB-6 on the Growth of Replanted Apple Trees and the Soil Microbial Environment. Horticulturae 2022, 8, 83. [Google Scholar] [CrossRef]
  69. Vahedi, R.; Rasouli-Sadaghiani, M.H.; Barin, M.; Vetukuri, R.R. Effect of Biochar and Microbial Inoculation on P, Fe, and Zn Bioavailability in a Calcareous Soil. Processes 2022, 10, 343. [Google Scholar] [CrossRef]
  70. Przybyłko, S.; Kowalczyk, W.; Wrona, D. The Effect of Mycorrhizal Fungi and PGPR on Tree Nutritional Status and Growth in Organic Apple Production. Agronomy 2021, 11, 1402. [Google Scholar] [CrossRef]
  71. Srivastava, A.K.; Wu, Q.S.; Mousavi, S.M.; Hota, D. Integrated Soil Fertility Management in Fruit Crops: An Overview. Int. J. Fruit Sci. 2021, 21, 413–439. [Google Scholar] [CrossRef]
  72. Essalimi, B.; Esserti, S.; Rifai, L.A.; Koussa, T.; Makroum, K.; Belfaiza, M.; Rifai, S.; Venisse, J.S.; Faize, L.; Alburquerque, N.; et al. Enhancement of plant growth, acclimatization, salt stress tolerance and verticillium wilt disease resistance using plant growth-promoting rhizobacteria (PGPR) associated with plum trees (Prunus domestica). Sci. Hortic. 2022, 291, 110621. [Google Scholar] [CrossRef]
  73. Karakurt, H.; Kotan, R.; Aslantas, R.; Dadasoglu, F.; Karagöz, K. Inoculation effects of pantoea agglomerans strains on growth and chemical composition of plum. J. Plant Nutr. 2010, 33, 1998–2009. [Google Scholar] [CrossRef]
  74. Bonaterra, A.; Ruz, L.; Badosa, E.; Pinochet, J.; Montesinos, E. Growth promotion of Prunus rootstocks by root treatment with specific bacterial strains. Plant Soil 2003, 255, 555–569. [Google Scholar] [CrossRef]
  75. Gani, G.; Asif, M.; Wani, P.A.; Malik, M.A.; Dar, Z.M.; Masood, A.; Shafi, S. Chlorpyrifos degradation, biocontrol potential and antioxidant defence activation under pesticide stress by rhizosphere bacteria isolated from rhizosphere of peach (Prunus persica) plants. Chem. Ecol. 2021, 37, 866–881. [Google Scholar] [CrossRef]
  76. Arıkan, Ş.; Eşitken, A.; İpek, M.; Aras, S.; Şahin, M.; Pırlak, L.; Dönmez, M.F.; Turan, M. Effect of Plant Growth Promoting Rhizobacteria on Fe Acquisition in Peach (Prunus persica L.) Under Calcareous Soil Conditions. J. Plant Nutr. 2018, 41, 2141–2150. [Google Scholar] [CrossRef]
  77. Gharbi-Hajji, H.; Sanaa, M. Enhancement of Nutrient Uptake in Peach Rootstock with Arbuscular Mycorrhizal Fungi and Plant-Growth Promoting Rhizo-Bacteria Inoculation in Nursery. In Proceedings of the Fifth International Scientific Agricultural Symposium “Agrosym 2014”, Jahorina, Bosnia and Herzegovina, 23–26October 2014; University of East Sarajevo, Faculty of Agriculture: Lukavica, Bosnia and Herzegovina, 2014. [Google Scholar]
  78. Chang, H.; Yang, H.; Han, T.; Wang, F.; Liu, Y. Study on the optimal antagonistic effect of a bacterial complex against Monilinia fructicola in peach. Open Life Sci. 2020, 15, 890–901. [Google Scholar] [CrossRef]
  79. Ipek, M.; Arıkan, Ş.; Eşitken, A.; Pırlak, L.; Dönmez, M.F.; Turan, M. Influence of Bacterial Inoculation on Growth and Plant Nutrition of Peach Grafted in Different Rootstocks in Calcareous Soil. Sains Malays. 2021, 50, 2615–2624. [Google Scholar] [CrossRef]
  80. Gallart, M.; Paungfoo-Lonhienne, C.; Trueman, S.J. Effects of a growth-promoting Paraburkholderia species on nitrogen acquisition by avocado seedlings. Sci. Hortic. 2022, 295, 110767. [Google Scholar] [CrossRef]
  81. Tzec-Interián, J.A.; Desgarennes, D.; Carrión, G.; Monribot-Villanueva, J.L.; Guerrero-Analco, J.A.; Ferrera-Rodríguez, O.; Santos-Rodríguez, D.L.; Liahut-Guin, N.; Caballero-Reyes, G.E.; Ortiz-Castro, R. Characterization of plant growth-promoting bacteria associated with avocado trees (Persea americana Miller) and their potential use in the biocontrol of Scirtothrips perseae (avocado thrips). PLoS ONE 2020, 15, e0231215. [Google Scholar] [CrossRef] [Green Version]
  82. Ali, M.A.; Luo, J.; Ahmed, T.; Zhang, J.; Xie, T.; Dai, D.; Jiang, J.; Zhu, J.; Hassan, S.; Alorabi, J.A.; et al. Pseudomonas bijieensis Strain XL17 within the P. corrugata Subgroup Producing 2,4-Diacetylphloroglucinol and Lipopeptides Controls Bacterial Canker and Gray Mold Pathogens of Kiwifruit. Microorganisms 2022, 10, 425. [Google Scholar] [CrossRef] [PubMed]
  83. Shen, H.; He, X.; Liu, Y.; Chen, Y.; Tang, J.; Guo, T. A complex inoculant of N2-fixing, P- and K-solubilizing bacteria from a purple soil improves the growth of kiwifruit (Actinidia chinensis) plantlets. Front. Microbiol. 2016, 7, 841. [Google Scholar] [CrossRef] [PubMed]
  84. Erturk, Y.; Ercisli, S.; Haznedar, A.; Cakmakci, R. Effects of plant growth promoting rhizobacteria (PGPR) on rooting and root growth of kiwifruit (Actinidia deliciosa) stem cuttings. Biol. Res. 2010, 43, 91–98. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  85. Ercisli, S.; Esitken, A.; Cangi, R.; Şahin, F. Adventitious root formation of kiwifruit in relation to sampling date, IBA and Agrobacterium rubi inoculation. Plant Growth Regul. 2003, 41, 133–137. [Google Scholar] [CrossRef]
  86. Fan, L.; Zhou, X.; Li, Y.; Ji, L.; Wu, G.; Li, B.; Cheng, L.; Long, M.; Deng, W.; Zou, L. The influence of effective microorganisms on microbes and nutrients in kiwifruit planting soil. Appl. Sci. 2016, 6, 168. [Google Scholar] [CrossRef] [Green Version]
  87. Zhu, Y.; Li, W.; Ren, Y.; Huang, S.; Liu, Y. Azospirillum Actinidiae sp. nov., a Nitrogen-Fixing Bacterium Isolated from The Roots of Kiwifruit Plants. Res. Sq. 2021, 1–18. [Google Scholar] [CrossRef]
  88. Giassi, V.; Kiritani, C.; Kupper, K.C. Bacteria as growth-promoting agents for citrus rootstocks. Microbiol. Res. 2016, 190, 46–54. [Google Scholar] [CrossRef]
  89. Vives-Peris, V.; Gómez-Cadenas, A.; Pérez-Clemente, R.M. Salt stress alleviation in citrus plants by plant growth-promoting rhizobacteria Pseudomonas putida and Novosphingobium sp. Plant Cell Rep. 2018, 37, 1557–1569. [Google Scholar] [CrossRef]
  90. Thokchom, E.; Kalita, M.C.; Talukdar, N.C. Isolation, screening, characterization, and selection of superior rhizobacterial strains as bioinoculants for seedling emergence and growth promotion of Mandarin orange (Citrus reticulata Blanco). Can. J. Microbiol. 2014, 60, 85–92. [Google Scholar] [CrossRef]
  91. Andra, C.B.; Carlos, I.A.V.; Aline, A.C.N.; Welington, L.A. Effects of growth-promoting endophytic Methylobacterium on development of Citrus rootstocks. Afr. J. Microbiol. Res. 2016, 10, 646–653. [Google Scholar] [CrossRef] [Green Version]
  92. De Queiroz, B.P.V.; De Melo, I.S. Antagonism of Serratia marcescens towards Phytophthora parasitica and its effects in promoting the growth of citrus. Braz. J. Microbiol. 2006, 37, 448–450. [Google Scholar] [CrossRef] [Green Version]
  93. Sudyoung, N.; Tokuyama, S.; Krajangsang, S.; Pringsulaka, O.; Sarawaneeyaruk, S. Bacterial antagonists and their cell-free cultures efficiently suppress canker disease in citrus lime. J. Plant Dis. Prot. 2020, 127, 173–181. [Google Scholar] [CrossRef]
  94. Riera, N.; Handique, U.; Zhang, Y.; Dewdney, M.M.; Wang, N. Characterization of antimicrobial-producing beneficial bacteria isolated from Huanglongbing escape citrus trees. Front. Microbiol. 2017, 8, 2415. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  95. Ginnan, N.A.; Dang, T.; Bodaghi, S.; Ruegger, P.M.; McCollum, G.; England, G.; Vidalakis, G.; Borneman, J.; Rolshausen, P.E.; Caroline Roper, M. Disease-induced microbial shifts in citrus indicate microbiome-derived responses to huanglongbing across the disease severity spectrum. Phytobiomes J. 2020, 4, 375–387. [Google Scholar] [CrossRef]
  96. Keswani, C.; Prakash, O.; Bharti, N.; Vílchez, J.I.; Sansinenea, E.; Lally, R.D.; Borriss, R.; Singh, S.P.; Gupta, V.K.; Fraceto, L.F.; et al. Re-addressing the biosafety issues of plant growth promoting rhizobacteria. Sci. Total Environ. 2019, 690, 841–852. [Google Scholar] [CrossRef]
Figure 1. The core concept of sustainability and the interactions between the different dimensions.
Figure 1. The core concept of sustainability and the interactions between the different dimensions.
Sustainability 14 13952 g001
Figure 2. Overall visualization of the interconnections between different components in a soil ecosystem.
Figure 2. Overall visualization of the interconnections between different components in a soil ecosystem.
Sustainability 14 13952 g002
Figure 3. Common desirable features that are targets of study to overcome frequent hurdles.
Figure 3. Common desirable features that are targets of study to overcome frequent hurdles.
Sustainability 14 13952 g003
Table 1. Description of the main sustainable practices and systems.
Table 1. Description of the main sustainable practices and systems.
DescriptionExamples of Expected ImpactReference
Management Practices[15,16,17]
Cover crops and green manureProvide constant soil cover.Increase SOM; nutrient mobilization; decrease emergence of pests and pathogens.
Crop rotationSequence of different crops cultivated on the same land, with different temporal frames.Use of different soil nutrient combinations to avoid over-exploiting the soil ecosystem.
Reduced tillageReduce mechanical disturbance of the soil.Avoid soil parameters degradation (e.g., carbon sequestration, soil density, water holding capacity).
IntercroppingCultivating different crops species on the same field simultaneously.Improve nitrogen fixation and other nutrient cycles; obtain soil cover; decrease emergence of pests and pathogens.
Structural elementsFeatures in the landscape and techniques implemented or managed by the farmer.Decrease impact of weather; improve light accessibility.
Irrigation managementControl the amount of water supplied.Maintain optimal humidity levels; avoid nutrients leaching; decrease water loss.
Allowed External Inputs
Organic fertilizerApplication of animal manure.Supplement the Orchard with the required nutrients; improve soil quality.
CompostAerobically decomposed organic matter
VermicompostOrganic material decomposed by earthworms.
BiofertilizersGrowth-promoting bacteria or fungus.
FertigationWater fortified with nutrients and controlled administration.
Sustainable Agriculture Systems
Conservation AgricultureCombination of three principals
  • Minimal mechanical soil disturbance
  • Permanent soil cover by crop residues, cover crops and mulching.
  • Diverse crop rotation or mixture.
Crop-Livestock systemsIntegration of crops with live stocks.
Organic AgricultureAbsence of agrochemical inputs, relying on ecological processes and biodiversity.
AgroforestryIntegrations of trees and crops in the same land. Integration of woody and herbaceous layers.
Table 2. Main macronutrients and their influence on plants.
Table 2. Main macronutrients and their influence on plants.
NutrientsUptake FormSoil ConditionsBiological FunctionsPlant Impact/DeficiencyStratificationReferences
Nitrogen (N)NH4+Low pH and reducing soil conditions.Contribute to amino acid formation; energy homeostasis, signaling and protein regulation. Essential for co-enzymes, photosynthetic pigments, secondary metabolites and polyamines.Stunted growth, small leaves, reduced shoot branching and early flowering. Often anthocyanosis on leaf and stem.acropetal[31,33,34,36,37,38,39,40]
NO3Higher pH and aerobic conditions.
Phosphorous
(P)
H2PO4Available form is pH dependent.
Natural availability is very slow.
Uptake is improved by the presence of mycorrhizal symbioses.
Cellular energy homoeostasis; component of nucleic acids; structural role in cellular membranes; reversible protein phosphorylation; cellular metabolism. P deficiency causes a rapid decrease in photosynthetic rates. Anthocyanosis. Dark-green and/or purple leaves.Acropetal
Potassium (K)Other forms: solution K, exchangeable K, “fixed” K, structural K in primary mineralsK+ is dehydrated and coordinated with oxygen atoms not available to plants.
K solubilization is driven by water.
Metabolic reactions and enzyme activity. Ribosome mediated protein synthesis. Accumulation of reducing sugars and depletion of organic acids; turgor provision and water homeostasis. K demand is strongest during fruit development.Accelerate premature leaf senescence and reduce numbers of flowers and fruits in subsequent years. Chlorosis on tip of oldest leaves that develop into marginal necrosis. Bronzing. Slack appearance due to poor turgor and stomatal control.Acropetal
Calcium (Ca)Ca2+Ca2+ adsorbed to colloids can be exchanged with the soil solution where much of the ‘free’ Ca2+ forms nearly insoluble compounds with other elements such as phosphorus, thus making P less available.Structural and secondary messenger.
Rigidity to cell walls and membrane structure.
Ca2+ levels may fall below a critical level in fast-growing tissues causing diseases such as ‘black heart’ in celery, ‘blossom end rot’ in tomatoes or ‘bitter-pit’ in apples. Disintegration of root tissue. Necrotic lesions on leaf edges and tips. Meristem death. Necrotic spots on fruits and vegetables. Leaf deformity.Basipetal
Magnesium (Mg)Mg2+Adsorption to soil particles is relatively weak which results in high leaching rates and Mg2+ deficiency is therefore common.Central position in the chlorophyll molecule; signal element in chloroplast development; roles as enzyme cofactors associated with energy transfer.Intravenous chlorosis on oldest leaves that eventually develop into necrosis. Accumulation of sucrose and starch in chloroplast.Acropetal
Sulfur (S) In saline and sodic soils, inorganic salts are predominant.Amino acids; protein activity reductant in the detoxification of reactive oxygen species.oChlorosis of young leaves. Stunted growth. Anthocyanosis; S toxicity is rare but can occur in saline soils with high levels of SO42− salts, and atmospheric pollution.Basipetal
SO42−In aerobic conditions.
FeS, FeS2 and H2SReducing environment created by flooding.
SO42 and H2S.Extracted from atmosphere.
Stratification: Basipetal, symptoms first appear on youngest leaves; acropetal, symptoms first appear on oldest leaves. NH4+—ammonium cation; NO3—Nitrate; H2PO4—Dihydrogen phosphate; SO42−—Sulfate; FeS—Iron sulfide; FeS2—Iron disulfide; H2S—Hydrogen sulfite.
Table 3. Micronutrients and their influence on plants.
Table 3. Micronutrients and their influence on plants.
NutrientSoil AvailabilityBiological FunctionDeficiencyStratificationReference
Iron (Fe)Maximum availability in acidic pH range and decreases drastically with increase in pH. Excessive water and poor aeration, organic matter, interaction with other nutrients effect control Fe availability.Synthesis of chlorophyllLeaves exhibit pale color and veins remains green or interveinal chlorosis of the whole leaves. Papery white color of the leaves occurs under severe deficiency.Basipetal[41,42]
Manganese (Mn)Soluble Mn (Mn2+) is rapidly converted to plant-unavailable Mn oxides, particularly in sandy alkaline soils. Disorder in soils with high pH and high partial pressure of O2.Enzyme activity.
Oxidation-reduction processes.
Synthesis of chlorophyll,
Similar to Fe deficiency, with pale leaves and green veins. Sometimes brown, black or grey spots are observed next to leaf veins. Chlorosis up to leaf margins followed by browning and necrosis.Acropetal[41,43]
Zinc (Zn)Low content in the rocks/minerals, soil pH, presence of calcium carbonate, soil redox potential, clay content, soil moisture status. Positive interaction with nitrogen (N) and potassium (K). Negative interactions with phosphorus (P), calcium (Ca), iron (Fe), and copper (Cu).Regulation of plant growth and transformation of carbohydrates. Required for nucleic acid synthesis and enzyme activationInterveinal chlorosisBasipetal[41,42]
Copper (Cu)Availability decreases with high pH, high soil organic carbon and high clay contentEnzyme system that utilizes carbohydrates and proteins and is important for reproductive growth.Dieback of shoot tips; old leaves develop brown spots. Male flower sterility, delay flowering and senescence.Acropetal[41,44]
Boron (B)Increasing soil pH decreases B availability by increasing B adsorption onto clay and Al and Fe hydroxyl surfaces, especially at high soil pHRequired for nucleic acid synthesis, pollen germination and the growth of the pollen tube. Promotes root development, enzyme activity, lignin synthesis, sugar transport, seed and cell wall formation, calcium uptake and water relations. Imparts drought tolerance to the cropsCurled, brittle leaves; discolored or cracked fruits. Leaf symptoms found on leaf tips and terminal buds or the youngest leaves, which become discolored and may die under acute deficient conditions. Development of water-soaked areas on the leaves, development of corky tissues and purpling or yellowing of interveinal portion of young leaves.Basipetal[41,45,46]
Table 4. Nutritional requirements of some fruit trees.
Table 4. Nutritional requirements of some fruit trees.
NutrientsKiwiApplePeach and PlumPomegranateCitrus
DeficitNormalExcessDeficitNormalExcessDeficitNormalExcessDeficitNormalExcessDeficitNormalExcess
N-23–28 e-<1.6 a2.0–2.4 a>3.0 a1.72.4–3.04.0->2.0-<2.2 a2.5–2.7 a>3.0 a
P-1.6–2.0 e-<0.10 a0.15–0.20 a>0.3 a0.090.14–0.250.4-0.13–0.15-<0.09 a0.12–0.16 a>0.30 a
K-12–19 e-<0.8 a1.1–1.5 a>2.0 a1.01.6–3.04.0-1.0–1.2-<0.7 a1.2–1.7 a>2.4 a
Ca-33–44 e-<0.7 a1.1–2.0 a>2.5 a1.01.5–3.04.0-4.5–4.9-<1.5 a3.0–4.9 a>7.0 a
Mg-4.0–11 e-<0.18 a0.25–0.35 a>0.5 a0.20.3–0.81.10-0.38–0.42-<0.2 a0.30–0.49 a>0.7 a
Cl-6.0–10 e--<0.4 a>1.0 a-------0.05–0.10 a>0.25 a
Na-<500 b--<0.02 a>0.5 a-------->0.25 a
Mn-44–173 b-<20 c25–100 c>200 c20 c40–160 c400 c-30–45 d-<17 b25–100 b>300 b
Zn-26–44 b-<10 c16–50 c>50 c15 c20–50 c70 c-14–15 d-<17 b25–100 b>300 b
Cu-7.0–22 b-<4 c6–20 c>21 c4 c4–16 c30 c-4.5–7.0 d-<3 b5–16 b>20 b
Fe-90–268 b-->50 c-60 c100–250 c500 c-70–85 d-<35 b60–120 b>200 b
B-39–80 b-<15 c20–60 c>200 c20 c25–60 c80 c-20–22 d-<20 b36–100 b>200 b
Reference[47][48,49][22,50][26,51][35]
a Dry weight %; b mg/kg; c ppm; d mg/L; e g/kg.
Table 5. PGPB studies on fruit orchards.
Table 5. PGPB studies on fruit orchards.
Fruit CropMicroorganismsParameters EvaluatedReference
AppleAzotobacter chroococcum, Bacillus subtilis, Bacillus megateriumFruit yield, Nutrient efficiency[62]
Bacillus spp., Burkholderia spp., Pseudomonas spp.Growth, Fruit yield[63]
Pseudomonas putid, Bacillus subtilisFoliar application[64]
Alcaligenes spp., Agrobacterium spp., Staphylococcus spp., Bacillus spp., Pantoea sp.Iron acquisition[65]
Pseudomonas fluorescensDrought stress, Nutrient uptake, root grow [66]
Bacillus sp., Bacillus amyloliquefaciens, Paenibacillus polymyxaNutrient composition of apple leaves[67]
Bacillus amyloliquefaciensGrowth[68]
Pseudomonas aeruginosa, Pseudomonas fluorescens, Pseudomonas putidaSoil properties; Nutrient availability [69]
Bacillus subtilis; Streptomyces spp.Nutritional status; Growth[70]
PomegranateAzotobacter chroococcumPlant canopy, Pruned material, Fruit yield[71]
PlumPseudomonas stutzeri; Bacillus toyonensisGrowth; Acclimatization; Disease tolerance[72]
Pantoea agglomeransFruit traits; Chemical composition[73]
Pseudomonas fluorescens; Pantoea agglomeransRootstock growth[74]
PeachBacillus flexusDisease tolerance; Growth [75]
Alcaligenes sp., Agrobacterium sp., Staphylococcus sp., Bacillus sp. and Pantoea sp. Iron acquisition[76]
Azospirillum sp.; Frateuria aurantia; Bacillus megateriumNutrient uptake; Growth[77]
Bacillussubtilis; Bacillustequilensis; BacillusmethylotrophicusDisease tolerance[78]
Alcaligenes spp., Agrobacterium spp., Staphylococcus spp., Bacillus spp. and Pantoea spp.Growth and Nutrient content [79]
AvocadoParaburkholderia sp.Growth; Nitrogen acquisition,[80]
Pseudomonas sp., Serratia sp. and Stenotrophomona sp.Disease tolerance[81]
KiwiPseudomonas bijieensisDisease tolerance[82]
Bacillus amyloliquefaciens, Bacillus pumilus, Bacillus circulans,Growth promotion; Nutrient uptake[83]
Paenibacillus polymyxa; Comamonas acidovorans, Bacillus sp. Root growth[84]
Agrobacterium rubiRoot growth[85]
Bacillus subtilis, Bacillus stearothermophilus, Bacillu amyloliquefaciens, Actinobacteria sp.Impact on soil nutrients[86]
Azospirillum actinidiaeNitrogen fixation[87]
CitrusBacillus sp.; Lactic acid bacteria; Actinobacteria sp.;IAA production; Nutrient availability[88]
Pseudomonas putida; Novosphingobium sp.Salt stress[89]
Enterobacter hormaechei; Enterobacter asburiae; Enterobacter ludwigii; Klebsiella pneumoniaeGrowth performance[90]
Methylobacterium sp.Rootstock development[91]
Serratia marcescenDisease tolerance; Growth promotion[92]
Bacillus velezensis, Pseudomonas aeruginosaDisease tolerance[93]
Rhodococcus sp., Burkholderia sp.Disease tolerance; Growth promotion[94]
Bacillus sp., Lactobacillus sp., Streptomyces sp., Methylobacterium sp., Hymenobacter sp., Pantoea sp., Curtobacterium sp., Spirosoma sp.Disease tolerance[95]
IAA—indole acetic acid.
Publisher’s Note: MDPI stays neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Share and Cite

MDPI and ACS Style

Freitas, J.; Silva, P. Sustainable Agricultural Systems for Fruit Orchards: The Influence of Plant Growth Promoting Bacteria on the Soil Biodiversity and Nutrient Management. Sustainability 2022, 14, 13952. https://doi.org/10.3390/su142113952

AMA Style

Freitas J, Silva P. Sustainable Agricultural Systems for Fruit Orchards: The Influence of Plant Growth Promoting Bacteria on the Soil Biodiversity and Nutrient Management. Sustainability. 2022; 14(21):13952. https://doi.org/10.3390/su142113952

Chicago/Turabian Style

Freitas, Jorge, and Pedro Silva. 2022. "Sustainable Agricultural Systems for Fruit Orchards: The Influence of Plant Growth Promoting Bacteria on the Soil Biodiversity and Nutrient Management" Sustainability 14, no. 21: 13952. https://doi.org/10.3390/su142113952

Note that from the first issue of 2016, this journal uses article numbers instead of page numbers. See further details here.

Article Metrics

Back to TopTop