• Nutrient distribution and neighbours can impact plant growth, but how neighbours shape root-foraging strategy for nutrients is unclear. Here, we explore new patterns of plant foraging for nutrients ...as affected by neighbours to improve nutrient acquisition.
• Maize (Zea mays) was grown alone (maize), or with maize (maize/maize) or faba bean (Vicia faba) (maize/faba bean) as a neighbour on one side and with or without a phosphorus (P)-rich zone on the other in a rhizo-box experiment.
• Maize demonstrated root avoidance in maize/maize, with reduced root growth in ‘shared’ soil, and increased growth away from its neighbours. Conversely, maize proliferated roots in the proximity of neighbouring faba bean roots that had greater P availability in the rhizosphere (as a result of citrate and acid phosphatase exudation) compared with maize roots. Maize proliferated more roots, but spent less time to reach, and grow out of, the P patches away from neighbours in the maize/maize than in the maize/faba bean experiment. Maize shoot biomass and P uptake were greater in the heterogeneous P treatment with maize/faba bean than with maize/maize system.
• The foraging strategy of maize roots is an integrated function of heterogeneous distribution of nutrients and neighbouring plants, thus improving nutrient acquisition and maize growth. Understanding the foraging patterns is critical for optimizing nutrient management in crops.
The role of amorphous silica nanoparticles (SiNPs) in enhancing growth and yield of cucumber under water deficit and salinity stresses was assessed. A field experiment under greenhouse conditions was ...established using 4 different levels of SiNPs (100, 200, 300 and 400 mg kg−1) and 3 different watering regimes calculated based on crop evapotranspiration (ETc) (100, 85 and 70% of ETc). Electrical conductivity and sodium adsorption ratio of irrigation water were 1.7 dS m−1 and 4.63 respectively. The results revealed that SiNPs improved growth and productivity of cucumber regardless of quantity of supplied water; however, the greatest increase corresponded to irrigating cucumber at the rate of 85% of ETc. Applying SiNPs at rate of 200 mg kg−1 showed the greatest increase specially when cucumber plants received 85% of their ETc causing an increase of 20, 51 and 156% in plant height, chlorophyll and fruit yield, respectively, compared to untreated plants. These increases could be due to alerting nutrient uptake as SiNPs clearly increased contents of nitrogen (by 30%), potassium (by 52, 75 and 41% in root, stem and leaf, respectively) and silicon (by 51, 57, 8 and 78% in root, stem, leaf and fruit, respectively). Otherwise, same treatment reduced sodium uptake by 38, 77 and 38% in root, stem and leaf, respectively; consequently, potassium-sodium ratio increased by 149, 735 and 127% in root, stem and leaf, respectively. The significant role of SiNPs in mitigating water deficit and salinity stresses could be referred to high silicon content found in leaf which regulates water losses via transpiration. Also, high K+ content found in roots of cucumber helps plants to tolerate abiotic stresses as a result of maintaining ion homeostasis and regulating the osmotic balance as well as controlling stomatal opening which helps plants to adapt to salinity and water deficit stresses.
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•Reducing water supply by 30% of ETc decreased growth and yield of cucumber.•Applying SiNPs enhanced cucumber yield under water deficit and salinity stress.•200 mg kg−1 SiNPs increased fruit yield with reduction in water supply by 15%.•SiNPs enhanced water and nutrient use efficiencies as well as balanced nutrient uptake.
Efficient resource use is a key factor for sustainable production and a necessity for meeting future global food demands. However, the factors that control resource use efficiency in agro‐ecosystems ...are only partly understood. We investigated the influence of soil biota on nutrient leaching, nutrient‐use efficiency and plant performance in outdoor, open‐top lysimeters comprising a volume of 230 L. The lysimeters were filled with sterilized soil in two horizons and inoculated with a reduced soil‐life inoculum (soil biota ≤11 μm, microbially dominated) and an enriched soil‐life inoculum soil organisms ≤2 mm, also containing arbuscular mycorrhizal fungi (AMF). A crop rotation was planted, and nutrient leaching losses, plant biomass and nutrient contents were assessed over a period of almost 2 years. In the first year of the experiment, enriched soil life increased crop yield (+22%), N uptake (+29%) and P uptake (+110%) of maize and strongly reduced leaching losses of N (−51%, corresponding to a reduction of 76 kg N ha⁻¹). In the second year, wheat biomass (+17%) and P contents (+80%) were significantly increased by enriched soil life, but the differences were lower than in the first year. Enriched soil life also increased P mobilization from soil (+112%) and significantly reduced relative P leaching losses (−25%), defined as g P leached per kg P plant uptake, as well as relative N leaching losses (−36%), defined as kg N leached per kg N plant uptake, demonstrating that nutrient‐use efficiency was increased in the enriched soil‐life treatment. Synthesis and applications. Soil biota are a key factor determining resource efficiency in agriculture. The results suggest that applying farming practices, which favour a rich and abundant soil life (e.g. reduced tillage, organic farming, crop rotation), can reduce environmental impacts, enhance crop yield and result in a more sustainable agricultural system. However, this needs to be confirmed in field situations. Enhanced nutrient‐use efficiency obtained through farming practices which exert positive effects on soil biota could result in reduced amounts of fertilisers needed for agricultural production and reduced nutrient losses to the environment, providing benefits of such practices beyond positive effects on biodiversity.
•We review the use of commercial bio-inoculants to increase plant uptake of phosphorus.•We examine microorganisms found within such bio-inoculants and their mode of action.•We propose a re-order of ...nomenclature to clarify the typology of bio-inoculants.•We conclude that the beneficial attributes of commercial bio-inoculants are unclear.•However, bio-inoculants could contribute to sustainable food production systems.
Meeting increasing global demand for food, fibre, and bioenergy requires efficient use of finite resources, and presents a key sustainability challenge to the agricultural industry, scientists and policy-makers. Increased interest in low-input agriculture in recent years has seen the growing development and use of commercial biological inoculants (bacteria and/or fungi) to increase the mobilisation of key nutrients, especially phosphorus (P), and enhance their availability to crop plants. Here, we review the terminology, composition and function of bio-inoculants and the many factors which impact on their efficacy for increasing P availability in different soil and plant environments. We conclude that the beneficial attributes of commercial bio-inoculants for integrated production systems are not clearly defined. Evidence to support their effectiveness is currently confounded by inadequate quality standards and insufficient knowledge of the underlying mechanisms, which have led to contradicting reports on field performance. There is, however, scope to engineer specific inoculant formulae for more sustainable P management in different system-soil-plant combinations, provided future research is properly structured to help understand the complexity and dynamism of microbial functioning and interactions in soils.
Tomorrow's agriculture, challenged by increasing global demand for food, scarcity of arable lands, and resources alongside multiple environment pressures, needs to be managed smartly through ...sustainable and eco-efficient approaches. Modern agriculture has to be more productive, sustainable, and environmentally friendly. While macronutrients such as nitrogen (N), phosphorus (P), potassium (K), and sulfur (S) supplied by mineral fertilizers are vital to crop production, agriculturally beneficial microorganisms may also contribute directly (i.e., biological N
fixation, P solubilization, and phytohormone production, etc.) or indirectly (i.e., antimicrobial compounds biosynthesis and elicitation of induced systemic resistance, etc.) to crop improvement and fertilizers efficiency. Microbial-based bioformulations that increase plant performance are greatly needed, and in particular bioformulations that exhibit complementary and synergistic effects with mineral fertilization. Such an integrated soil fertility management strategy has been demonstrated through several controlled and non-controlled experiments, but more efforts have to be made in order to thoroughly understand the multiple functions of beneficial microorganisms within the soil microbial community itself and in interaction with plants and mineral resources. In fact, the combined usage of microbial i.e., beneficial microorganisms: N
-fixing (NF), P-solubilizing, and P mobilizing, etc. and mineral resources is an emerging research area that aims to design and develop efficient microbial formulations which are highly compatible with mineral inputs, with positive impacts on both crops and environment. This novel approach is likely to be of a global interest, especially in most N- and P-deficient agro-ecosystems. In this review, we report on the importance of NF bacteria and P solubilizing/mobilizing microbes as well as their interactions with mineral P fertilization in improving crop productivity and fertilizers efficiency. In addition, we shed light on the interactive and synergistic effects that may occur within multi-trophic interactions involving those two microbial groups and positive consequences on plant mineral uptake, crop productivity, and resiliency to environmental constraints. Improving use of mineral nutrients is a must to securing higher yield and productivity in a sustainable manner, therefore continuously designing, developing and testing innovative integrated plant nutrient management systems based on relevant biological resources (crops and microorganisms) is highly required.
To avoid loss of yield, crops must maintain tissue potassium (K) concentrations above 5–40 mg K (g DM)–1. The supply of K from the soil is often insufficient to meet this demand and, in many ...agricultural systems, K fertilisers are applied to crops. However, K fertilisers are expensive. There is interest, therefore, in reducing applications of K fertilisers either by improving agronomy or developing crop genotypes that use K fertilisers more efficiently. Agronomic K fertiliser use efficiency is determined by the ability of roots to acquire K from the soil, which is referred to as K uptake efficiency (KUpE), and the ability of a plant to utilise the K acquired to produce yield, which is referred to as K utilisation efficiency (KUtE). There is considerable genetic variation between and within crop species in both KUpE and KUtE, and chromosomal loci affecting these characteristics have been identified in Arabidopsis thaliana and several crop species. Plant traits that increase KUpE include (1) exudation of organic compounds that release more non‐exchangeable soil K, (2) high root K uptake capacity, (3) early root vigour, high root‐to‐shoot ratios, and high root length densities, (4) proliferation of roots throughout the soil volume, and (5) high transpiration rates. Plant traits that increase KUtE include (1) effective K redistribution within the plant, (2) tolerance of low tissue K concentrations, and, at low tissue K concentrations, (3) maintenance of optimal K concentrations in metabolically active cellular compartments, (4) replacement of K in its non‐specific roles, (5) redistribution of K from senescent to younger tissues, (6) maintenance of water relations, photosynthesis and canopy cover, and (7) a high harvest index. The development of crop genotypes with these traits will enable K fertiliser applications to be reduced.
Schematic diagram of urea dissolution, diffusion and hydrolysis in the soil. (a) Without an inhibitor, hydrolysis is fast (dark blue color) causing NH3/NH4+ accumulation and increasing the pH close ...to the soil surface around the fertilizer granule, driving NH3 volatilization. As the ammonia species are less mobile in soil, diffusion is limited. (b) The inhibitor maintains urea unhydrolyzed for some time. Urea has no electrical charges and diffuses easily into the soil solution. When the effect of the inhibitor phases down and urea starts to hydrolyze, both the pH and the NH3/NH4+ concentrations are lower (light blue color) as a result of dilution. Part of the urea is incorporated into the soil before hydrolysis; the NH3 produced inside the soil is retained by the negative charges of colloidal material and losses are reduced even if no rain or irrigation incorporates urea into the soil.
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Urea is the most widely used nitrogen (N) fertilizer, with a projected increase in annual demand of 1.5% in the coming years. After its application to soil, urea undergoes hydrolysis via the urease enzyme, causing increases in the soil pH in the surrounding area of the granules and resulting in NH3 losses that average 16% of N applied worldwide and can reach 40% or more in hot and humid conditions. The use of urease inhibitors is an effective way to reduce NH3 losses. Several compounds act as urease inhibitors, but only N-(n-butyl) thiophosphoric triamide (NBPT) has been used worldwide, being the most successful in a market that has grown 16% per year in the past 10 years. Only in the past three years other compounds are being commercially launched. In comparison to urea, NBPT-treated urea reduces NH3 loss by around 53%. Yield gain by NBPT usage is of the order of 6.0% and varies from −0.8 to 10.2% depending on crop species. Nitrification inhibitors usually increase NH3 volatilization and mixing them with urease inhibitors partially offsets the benefits of the latter in reducing NH3 loss. The efficacy of NBPT to reduce NH3 loss is well documented, but there is a need for further improvement to increase the period of inhibition and the shelf life of NBPT-treated urea.
We evaluated the ecophysiological responses of two semiarid coniferous tree species, Pinus halepensis and Tetraclinis articulata, growing on a nutrient-poor metalliferous mine tailings substrate to ...organic amendments (biochar and/or organic municipal waste). The trees were grown in mesocosms under irrigated conditions for 20 months. Then, a comprehensive characterization of soil and plant parameters (including stable isotopes) was carried out. Treatments containing municipal waste showed better soil fertility indicators (approximately 2-fold higher organic carbon and total nitrogen concentrations) and higher plant biomass (up to 5-fold higher) than unamended and only biochar treatments. Trees in most of the treatments exhibited leaf N/P ratios <14 indicating severe N limitation of plant growth. Metal uptake was below phytotoxic levels across all the treatments. Leaf δ13C values correlated positively with δ18O across treatments for both species indicating increasing water use efficiency with tighter stomatal regulation of water flux, and with T. articulata exhibiting tighter stomatal control (higher δ18O values) than P. halepensis. Trees in treatments containing only biochar did not differ in ecophysiological performance from those in the unamended treatments. In contrast, leaf stable isotopes revealed sharply increased of time-integrated photosynthetic activity (favoured by higher leaf N concentrations) combined with lower time-integrated stomatal conductance in the treatments containing municipal waste, indicating greatly enhanced water use efficiency in better nourished plants. Trade-offs between water use efficiency and nutrient (N and P) use efficiency were evident across treatments, with higher leaf nutrient concentrations associated with higher water use efficiency, at the cost of a lower nutrient use efficiency. These trade-offs were not impaired by the high metal concentrations of the tailings substrate, indicating that ecophysiological adjustments in response to changes in plant nutrient status promoted by the addition of organic amendments are critical for the adaptability of native tree species employed in the phytostabilisation of mine tailings.
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•Organic amendments improve tree drought resistance and growth performance.•Better nourished plants were able to improve water use efficiency.•Metal uptake issues are not enough to fully explain tree adaptation to mine tailings.•A strong trade-off between water and nutrient use efficiency occurred in both trees.
Terrestrial microbial decomposer communities thrive on a wide range of organic matter types that rarely ever meet their elemental demands. In this review we synthesize the current state-of-the-art of ...microbial adaptations to resource stoichiometry, in order to gain a deeper understanding of the interactions between heterotrophic microbial communities and their chemical environment. The stoichiometric imbalance between microbial communities and their organic substrates generally decreases from wood to leaf litter and further to topsoil and subsoil organic matter. Microbial communities can respond to these imbalances in four ways: first, they adapt their biomass composition toward their resource in a non-homeostatic behavior. Such changes are, however, only moderate, and occur mainly because of changes in microbial community structure and less so due to cellular storage of elements in excess. Second, microbial communities can mobilize resources that meet their elemental demand by producing specific extracellular enzymes, which, in turn, is restricted by the C and N requirement for enzyme production itself. Third, microbes can regulate their element use efficiencies (ratio of element invested in growth over total element uptake), such that they release elements in excess depending on their demand (e.g., respiration and N mineralization). Fourth, diazotrophic bacteria and saprotrophic fungi may trigger the input of external N and P to decomposer communities. Theoretical considerations show that adjustments in element use efficiencies may be the most important mechanism by which microbes regulate their biomass stoichiometry. This review summarizes different views on how microbes cope with imbalanced supply of C, N and P, thereby providing a framework for integrating and linking microbial adaptation to resource imbalances to ecosystem scale fluxes across scales and ecosystems.
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