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2004, Resonance
AI
The paper discusses the critical importance of biodiversity and the role of various soil organisms in maintaining healthy soil ecosystems. It examines how environmental factors and human activities influence soil biological communities and their functions, particularly in nutrient cycling processes. The findings highlight the benefits of organic land management in enhancing soil structure and fertility, perils posed by unsustainable practices, and the implications for food security and ecosystem sustainability.
Biological nitrogen fixation (BNF) is an important N supply route for both natural vegetation and crop plants. The biological reduction of N2 to NH3 takes place at ambient temperature and sub ambient pressure and is performed by prokaryotes possessing the nitrogenase enzyme. Symbionts are the most significant N fixers for plants, and they are represented primarily by rhizobia (Protobacteria), Frankia (Actinomycetes), and Nostoc/Anabaena (Cyanobacteria). These organisms reside in specialized structures where they have access to a plentiful energy source in the form of photosynthates and an environment that is conducive both to nitrogenase activity and the translocation of fixed N directly to the host plant. Legumes have a special position among agricultural plants, as they have the ability to capture (fix) atmospheric N− through the presence of rhizobia in root nodules, which makes their growth theoretically independent both of soil N status and extraneous fertilizer N addition.
The capacity of bacteria and protozoa to mineralize soil nitrogen was studied in microcosms with sterilized soil with or without wheat plants. The effect of small additions of glucose or ammonium nitrate or both, twice a week was also tested. Plant dry weight and N-content, number of microorganisms and biomass plus inorganic N were determined after 6 weeks.
Bulletin of Environmental Contamination and Toxicology, 1993
Because of its rapidity and sensitivity, biological nitrogen fixation (BNF) has been studied widely in the laboratory and in the field since the invention of the acetylene reduction assay (ARA) (Hardy et al. 1973). The basis for the assay is the fact that nitrogenase, the enzyme complex in diazotrophic microorganisms that reduces nitrogen to ammonia, also reduces acetylene to ethylene (Schfllhorn and Burris 1967). The main objection is that it is an indirect measure of BNF, since no exact relationship exists between nitrogen fixation and acetylene reduction (Mayne 1984, ~nsson and Ljunggren 1984). Nonetheless, ARA has been used in ecological studies on BNF, including studies in aquatic systems on bluegreen algae, heterotrophic nitrogen fixing bacteria in soil, and legume symbiotic systems (Granhail and Lundgren 1971; Nohrstedt 1982; Wivstad et al. 1987). In particular, interesting field studies of ARA have been made on the effects of various pollutants on BNF activities by heterotrophic nitrogen fixing microorganisms and
Scientific Reports
Maize inoculation by Azospirillum stimulates root growth, along with soil nitrogen (N) uptake and root carbon (C) exudation, thus increasing N use efficiency. However, inoculation effects on soil N-cycling microbial communities have been overlooked. We hypothesized that inoculation would (i) increase roots-nitrifiers competition for ammonium, and thus decrease nitrifier abundance; and (ii) increase roots-denitrifiers competition for nitrate and C supply to denitrifiers by root exudation, and thus limit or benefit denitrifiers depending on the resource (N or C) mostly limiting these microorganisms. We quantified (de)nitrifiers abundance and activity in the rhizosphere of inoculated and non-inoculated maize on 4 sites over 2 years, and ancillary soil variables. Inoculation effects on nitrification and nitrifiers (AOA, AOB) were not consistent between the three sampling dates. Inoculation influenced denitrifiers abundance (nirK, nirS) differently among sites. In sites with high C limitation for denitrifiers (i.e. limitation of denitrification by C > 66%), inoculation increased nirS-denitrifier abundance (up to 56%) and gross N 2 O production (up to 84%), likely due to increased root C exudation. Conversely, in sites with low C limitation (<47%), inoculation decreased nirS-denitrifier abundance (down to −23%) and gross N 2 O production (down to −18%) likely due to an increased roots-denitrifiers competition for nitrate. The rhizosphere provides a peculiar environment where a huge variety of positive, negative and neutral interactions between roots and microorganisms occur 1. Such interactions can significantly influence plant growth as well as the functioning, the abundance and the diversity of rhizospheric microbial communities 2. Beneficial interactions are known to be established by plant growth-promoting rhizobacteria, PGPRs, with host plants through several mechanisms, including associative N 2 fixation, phosphate solubilization or phytosiderophore production 3, 4. This can result in improved root growth 5, 6 , increased number and length of lateral roots 7 , as well as an increased root and shoot biomass 8, 9 and physiology 10. The better root development induced by inoculation can consequently enhance nutrient 11 and water 12 uptake by plant, stimulate ion transport systems in root 13 and increase the amount of root carbon, C, exudation 14, 15. Azospirillum spp. are well-known PGPRs that are able to colonize the roots of many crop plant species including maize 16, 17. These PGPRs produce phytohormones that can promote root growth and improve nutrient and water absorption by plants 18-21. In particular, inoculation of cereal crops by PGPRs like the well-studied Azospirillum lipoferum CRT1 is often expected to improve crop capacity to retrieve mineral nitrogen, N, from soil. This could pave the way for improving the sustainability of these cropping systems under low N inputs conditions 8. However, inoculated plants could differently affect N dynamics in their rhizosphere, thus influencing the levels and types of mineral N forms available and possibly N losses from soil through leaching of nitrate, NO 3 − , or emission of nitrous oxide, N 2 O, a potent greenhouse gas 22 .
FEMS Microbiology Reviews, 2020
ABSTRACTNitrification is the microbial conversion of reduced forms of nitrogen (N) to nitrate (NO3−), and in fertilized soils it can lead to substantial N losses via NO3− leaching or nitrous oxide (N2O) production. To limit such problems, synthetic nitrification inhibitors have been applied but their performance differs between soils. In recent years, there has been an increasing interest in the occurrence of biological nitrification inhibition (BNI), a natural phenomenon according to which certain plants can inhibit nitrification through the release of active compounds in root exudates. Here, we synthesize the current state of research but also unravel knowledge gaps in the field. The nitrification process is discussed considering recent discoveries in genomics, biochemistry and ecology of nitrifiers. Secondly, we focus on the ‘where’ and ‘how’ of BNI. The N transformations and their interconnections as they occur in, and are affected by, the rhizosphere, are also discussed. The NH...
Trends in Ecology & Evolution, 1997
Plant and Soil, 1995
The competition for limiting amounts of ammonium between the chemolithotrophic ammonium-oxidizing species Nitrosomonas europaea, the heterotrophic species Arthrobacter globiformis and roots of Plantago lanceolata (Ribwort plantain) was studied in a series of model systems of increasing complexity, i.e. energy-limited continuous cultures, non-water-saturated continuously percolated soil columns and pots with "7-sterilized soil planted with axenic P. lanceolata seedlings. The effects of bacterial grazing by the flagellate species Adriamonas peritocrescens on the competition for ammonium were also investigated in the three model systems. It was found that N. europaea was a weaker competitor for ammonium than either A. globiformis or plant roots of P. lanceolata. It is assumed that the heterotrophic bacteria have a higher affinity for ammonium than the nitrifying bacteria, whereas growing plant roots have a greater capacity to exploit the soil for ammonium than the immobile nitrifying bacteria. It is not very likely that allelochemicals were involved in suppressing the nitrification process. Four reasons are given for this assumption. Presence of the flagellates strongly stimulated the potential nitrification rate in all model systems. It is assumed that there is a more even distribution over the soil of either nitrifying bacteria or their substrate ammonium in the presence of flagellates. In addition to the distribution effect, there is a stimulation of the potential ammonium oxidation rate. The results are discussed in the light of the function of nitrate as nitrogen sink in the biogeochemical nitrogen cycle.
Applied Soil Ecology, 2019
Soil microorganisms are essential to the functioning of soil ecosystems, and this study aimed to examine the effects of additions of carbon and nitrogen (N) to the soil on soil microflora, and whether these amendments could be used to both increase and reduce plant N concentrations in an orchard crop, thereby facilitating studies on the multitrophic interactions among the components of the orchard ecosystem. Sucrose or nitrogenous fertiliser was applied to the soil under sweet orange (Citrus × aurantium L.) trees; and respectively, reduced or increased plant N and chlorophyll concentrations. Next generation sequencing was used to examine bacterial and fungal populations within the test soils. Bacteria from 39 phyla or candidate phyla were found, together with fungi from 18 classes of seven different phyla. The relative abundances of these taxa were similar to those found in other studies with the exception of the Dormibacteraeota (AD3); this candidate phylum contained the fourth most abundant number of reads. For the bacterial populations, measures of alpha diversity in the soil given the fertiliser treatment were significantly lower than in the control; there was also a similar trend in the sugar treatment. The fungal data showed less difference among the treatments with no differences in the indices of alpha diversity. Measures of similarity/dissimilarity showed significant differences between treatments suggesting that both had reduced microbial biodiversity. The soil additions proved to be effective in manipulating tree N status thereby facilitating studies on other components of the orchard ecosystem. The consequences of the reductions in biodiversity due to the additions, and of the relative abundance of Dormibacteraeota on ecosystem functioning need to be determined. 2003; Liebig et al., 2006). Such effects may affect soil functions and ecosystem services. Soil microbial biomass is a major nutrient sink in many ecosystems (Harte and Kinzig, 1993) and may constitute an important control on nutrient availability, turnover and retention, particularly on the availability of N (Zogg et al., 2000; Clemmensen et al., 2008). A number of soil management practices have been used to deliberately reduce N availability. These include burning, grazing, biomass removal, topsoil removal and addition of carbon (C) to the soil, with the latter two treatments being reported as the most reliable (Perry et al., 2010). These practices have mainly been aimed at facilitating ecosystem management by reducing weed growth through decreases in available N. However, microbial nutrient immobilisation has also been reported in agricultural systems (Anderson and Domsch, 1989; Jensen et al., 1997), and C additions can stimulate the activity of soil microorganisms thereby immobilising plant-available soil nutrients including N
2020
Nitrogen (N), the most important element, is required by all living organisms for the synthesis of complex organic molecules like amino acids, proteins, lipids etc. Nitrogen cycle is considered to be the most complex yet arguably important cycle next to carbon cycle. Nitrogen cycle includes oxic and anoxic reactions like organic N mineralization, ammonia assimilation, nitrification denitrification, anaerobic ammonium oxidation (anammox), dissimilatory nitrate reduction to ammonium (DNRA), comammox, codenitrification etc. Nitrogen cycling is one of the most crucial processes required for the recycling of essential chemical requirements on the planet. Soil microorganisms not only improve N-cycle balance but also pave the way for sustainable agricultural practices, leading to improved soil properties and crop productivity as most plants are opportunistic in the uptake of soluble or available forms of N from soil. Microbial N transformations are influenced by plants to improve their nut...
Scientific Reports, 2017
Maize inoculation by Azospirillum stimulates root growth, along with soil nitrogen (N) uptake and root carbon (C) exudation, thus increasing N use efficiency. However, inoculation effects on soil N-cycling microbial communities have been overlooked. We hypothesized that inoculation would (i) increase roots-nitrifiers competition for ammonium, and thus decrease nitrifier abundance; and (ii) increase roots-denitrifiers competition for nitrate and C supply to denitrifiers by root exudation, and thus limit or benefit denitrifiers depending on the resource (N or C) mostly limiting these microorganisms. We quantified (de)nitrifiers abundance and activity in the rhizosphere of inoculated and non-inoculated maize on 4 sites over 2 years, and ancillary soil variables. Inoculation effects on nitrification and nitrifiers (AOA, AOB) were not consistent between the three sampling dates. Inoculation influenced denitrifiers abundance (nirK, nirS) differently among sites. In sites with high C limitation for denitrifiers (i.e. limitation of denitrification by C > 66%), inoculation increased nirS-denitrifier abundance (up to 56%) and gross N 2 O production (up to 84%), likely due to increased root C exudation. Conversely, in sites with low C limitation (<47%), inoculation decreased nirS-denitrifier abundance (down to −23%) and gross N 2 O production (down to −18%) likely due to an increased roots-denitrifiers competition for nitrate. The rhizosphere provides a peculiar environment where a huge variety of positive, negative and neutral interactions between roots and microorganisms occur 1. Such interactions can significantly influence plant growth as well as the functioning, the abundance and the diversity of rhizospheric microbial communities 2. Beneficial interactions are known to be established by plant growth-promoting rhizobacteria, PGPRs, with host plants through several mechanisms, including associative N 2 fixation, phosphate solubilization or phytosiderophore production 3, 4. This can result in improved root growth 5, 6 , increased number and length of lateral roots 7 , as well as an increased root and shoot biomass 8, 9 and physiology 10. The better root development induced by inoculation can consequently enhance nutrient 11 and water 12 uptake by plant, stimulate ion transport systems in root 13 and increase the amount of root carbon, C, exudation 14, 15. Azospirillum spp. are well-known PGPRs that are able to colonize the roots of many crop plant species including maize 16, 17. These PGPRs produce phytohormones that can promote root growth and improve nutrient and water absorption by plants 18-21. In particular, inoculation of cereal crops by PGPRs like the well-studied Azospirillum lipoferum CRT1 is often expected to improve crop capacity to retrieve mineral nitrogen, N, from soil. This could pave the way for improving the sustainability of these cropping systems under low N inputs conditions 8. However, inoculated plants could differently affect N dynamics in their rhizosphere, thus influencing the levels and types of mineral N forms available and possibly N losses from soil through leaching of nitrate, NO 3 − , or emission of nitrous oxide, N 2 O, a potent greenhouse gas 22 .
1986
1976
The major portion of the global nitrogen cycle occurs between vegetation and soil, only minor ex- changes generally taking place with the atmosphere and the hydrosphere. Nitrogen conversions in soil are briefly reviewed and a global flow chart for soil nitrogen is presented. The turnover times of nitro- gen in various components of this global system are compared with its
Management of Nitrogen and Phosphorus Fertilizers in Sub-Saharan Africa, 1986
The ISME Journal, 2011
The two-step nitrification process is an integral part of the global nitrogen cycle, and it is accomplished by distinctly different nitrifiers. By combining DNA-based stable isotope probing (SIP) and high-throughput pyrosequencing, we present the molecular evidence for autotrophic growth of ammonia-oxidizing bacteria (AOB), ammonia-oxidizing archaea (AOA) and nitrite-oxidizing bacteria (NOB) in agricultural soil upon ammonium fertilization. Time-course incubation of SIP microcosms indicated that the amoA genes of AOB was increasingly labeled by 13 CO 2 after incubation for 3, 7 and 28 days during active nitrification, whereas labeling of the AOA amoA gene was detected to a much lesser extent only after a 28-day incubation. Phylogenetic analysis of the 13 C-labeled amoA and 16S rRNA genes revealed that the Nitrosospira cluster 3-like sequences dominate the active AOB community and that active AOA is affiliated with the moderately thermophilic Nitrososphaera gargensis from a hot spring. The higher relative frequency of Nitrospira-like NOB in the 13 C-labeled DNA suggests that it may be more actively involved in nitrite oxidation than Nitrobacter-like NOB. Furthermore, the acetylene inhibition technique showed that 13 CO 2 assimilation by AOB, AOA and NOB occurs only when ammonia oxidation is not blocked, which provides strong hints for the chemolithoautotrophy of nitrifying community in complex soil environments. These results show that the microbial community of AOB and NOB dominates the nitrification process in the agricultural soil tested.
Biology and Fertility of Soils, 1991
Soil Science Society of America Journal, 2010
All rights reserved. No part of this periodical may be reproduced or transmitted in any form or by any means, electronic or mechanical, including photocopying, recording, or any information storage and retrieval system, without permission in writing from the publisher. Permission for printing and for reprinting the material contained herein has been obtained by the publisher. Nitrogen Transformations and Microbial Communities in Soil Aggregates from Three Tillage Systems Soil Biology & Biochemistry N o-till has several advantages over tilled systems, including increased water infi ltration, greater sequestration of soil organic matter, and reduction of soil erosion. Additionally, a body of literature has also demonstrated that soil N retention is greater in no-till than tilled systems (Alvarez et al., 1998; Beare et al., 1997). Plant-available N is not well defi ned for no-till systems, however, because during the transition from conventional tillage to no-till, particularly when C is accruing, increased microbial immobilization of inorganic N (Kitur et al., 1984; Rice and Smith, 1984) may temporarily reduce the plant-available N. As N immobilization and mineralization processes become more balanced, N availability to plants may become greater in no-till than in tilled soils (Rice et al., 1986). Information about the internal N cycle of no-till soils is limited. Th erefore, a thorough understanding of N cycling processes is required for formulation of the best N management practices in long-term no-till systems. Microbially mineralized NH 4 or NO 3 is also concurrently immobilized by soil microorganisms and recycled into the inorganic N pool due to the rapid turnover rate of the soil microbial biomass. Th us, the N dynamics resulting from the balance between mineralization and immobilization of inorganic N (both
European Journal of Soil Biology, 2016
Organic fertilizers are of high interest in agriculture as they promise a retarded release of the nitrogen to soil, which improves uptake efficiency by plants and reduces negative impacts like the formation of nitrate by nitrifiers or N 2 O by denitrifying microorganisms. In this study we tested the effects of seven different commercially available organic fertilizers of plant-, animal-, or microbial origin in a two-month greenhouse trial, using the perennial grass Cynodon dactylon in pots and monitoring effects on plant growth as well as on the abundance of prokaryotic nitrifiers and denitrifiers by realtime PCR. In most cases a single application of the fertilizers induced plant growth but did not increase the abundance of nitrifiers and denitrifiers. In contrast a repeated application stimulated, in addition to plant growth, also the increase of the two functional groups studied and a faster mobilization of nitrogen from the different fertilizers. Upon analyzing total bacterial DNA extracted from soil nirK abundance was found responsive to plant presence. Bacterial amoA and nosZ gene copies were significantly positively correlated with plant growth and cumulative dry weight at harvest. The latter was responsive as early as 9 days after fertilizer supplementation.
Plant and Soil, 1989
The possibility is examined that carbon (C) released into the soil from a root could enhance the availability of inorganic nitrogen (N) to plants by stimulating microbial activity. The release of soluble C compounds from roots is assumed to occur by one of two general processes: cortical cell death or exudation from intact cells. On the basis of several assumptions chosen to allow maximal amounts of N mineralisation to be calculated, greater amounts of net N mineralisation are theoretically possible at realistic soil C:N ratios if bacteria are grazed by predators such as protozoa, than if bacteria alone are active. More N is mineralised when the substrate released from the root has a high C:N ratio (as in cell death) than when it is relatively N-rich. The amounts of N that a root might realistically cause to be mineralised are unlikely to account entirely for high nitrate inflow rates that have been measured experimentally. However there are circumstances in which the loss of C from roots is essential if any N is to be mineralised and obtained by plants.
Agronomy, 2015
Agriculture is responsible for over half of the input of reactive nitrogen (N) to terrestrial systems; however improving N availability remains the primary management technique to increase crop yields in most regions. In the majority of agricultural soils, ammonium is rapidly converted to nitrate by nitrification, which increases the mobility of N through the soil matrix, strongly influencing N retention in the system. Decreasing nitrification through management is desirable to decrease N losses and increase N fertilizer use efficiency. We review the controlling factors on the rate and extent of nitrification in agricultural soils from temperate regions including substrate supply, environmental conditions, abundance and diversity of nitrifiers and plant and microbial interactions with nitrifiers. Approaches to the management of nitrification include those that control ammonium substrate availability and those that inhibit nitrifiers directly. Strategies for controlling ammonium substrate availability include timing of fertilization to coincide with rapid plant update, formulation of fertilizers for slow release or with inhibitors, keeping plant growing continuously to assimilate N, and intensify internal N cycling (immobilization). Another effective strategy is to inhibit nitrifiers directly with either synthetic or biological nitrification inhibitors. Commercial nitrification inhibitors are effective but their use is complicated by a changing climate and by organic management requirements. The interactions of the nitrifying organisms with plants or microbes producing biological nitrification inhibitors is a promising approach but just beginning to be critically examined. Climate smart agriculture will need to carefully consider optimized seasonal timing for these strategies to remain effective management tools.
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