Abstract
Nutrient stress is a worldwide problem which may alter the biochemical, physiological, and molecular processes in all kinds of plants. In addition, such nutritional stress is the major cause of malnutrition in the developing and poor countries. Generally, plants require 17 macro and micro nutrients for the optimum growth, development, and yield. Moreover, some other additional mineral elements are very crucial for the survival of the plants under stress conditions or help the farmer to produce the quality products. The proper and timely management could reduce its impacts. The impact of nutrient stress depends on plant age, soil types, plant species, ecology, climatic conditions, and genome of it. Usually, morphological characteristics of the plants are considered the quick, valuable, accurate, and strong identification of nutritional deficiency of the specific nutrients. Biochar (BC) is a cheap potential source of Carbon (C) which not only improves health and fertility of soil but also improves the quality and productivity of crops both in normal and under stress conditions. Here we reviewed that BC is the source of various kind of elements such as C, H, N, P, K, Mg, Ca, S and some other nutrients that are key for healthy plant growth. Moreover, it improves the soil physico-chemical properties such soil porosity, surface area, CEC, soil hydrophobic capacity, soil aeration and soil surface oxidation which results into increase in soil nutrients availability and further their retention in the rhizosphere. In conclusion, all these properties of BC could help the plant to survive under the nutrients stress conditions.
Access provided by Autonomous University of Puebla. Download chapter PDF
Similar content being viewed by others
Keywords
1 Introduction
The human global population will expected to reach 9.7 billion in 2050 (Rodés-Guirao 2013) and definitely will increase the demand of human food and feed requirements (Golden and Cotter 2021). Numerous abiotic stresses are threatening the global food security (Crandall et al. 2022). In addition to water and carbon dioxide, the plant growth needs balanced and sustainable nutrient acquisition to roots from soil for the production of carbohydrate (Amsili et al. 2021). Nutrient stress is a significant environmental factor that influences the plant growth and development (Bechtaoui et al. 2021). In addition, all stages of plant growth and development, including the whole plant, individual tissues and cells, and even subcellular levels are significantly affected (Holland et al. 2020). Some time, longer period of stress can harm plants by disturbing the protein aggregation and increased membrane lipids fluidity (Ogden et al. 2018; Li et al. 2020b). The healthy cell can create the cross link of different polymers and proteins and hence improve the stiffness of cell wall (Wang et al. 2016). The cell wall structure and components dictate the cell and tissue morphology depending the nutrient availability. Moreover, some time, it changes the pattern of cell growth and development (Ogden et al. 2018). The enzymes inactivation in mitochondria and chloroplast can be happened in some sever nutrient stress (Borysiuk et al. 2022).
Balanced proportions of macro-nutrients (carbon, hydrogen, oxygen, nitrogen, phosphorus, potassium, calcium, magnesium and sulfur and micro-nutrients (iron, zinc, manganese, copper, boron and molybdenum are vital for optimal growth and plant harvest (Pandey 2018). Nutrient stress could be resulted into nutrient specific phenotypes, growth inhibition, incomplete plant phenology and oftentimes, reorganization of root architecture (van der Bom et al. 2020; Al-Zahrani et al. 2022; Rajesh et al. 2022; Anam et al. 2021; Deepranjan et al. 2021; Haider et al. 2021; Amjad et al. 2021; Sajjad et al. 2021a, b; Fakhre et al. 2021; Khatun et al. 2021; Ibrar et al. 2021). Crops have some native ability in coping and tolerating these stress signals that communicate with one another (Bukhari et al. 2021; Haoliang et al. 2022; Sana et al. 2022; Abid et al. 2021; Zaman et al. 2021; Sajjad et al. 2021a, b; Rehana et al. 2021; Yang et al. 2022; Ahmad et al. 2022; Shah et al. 2022). The productive phase includes the development of male and female floral components, the variation of both gender flowery parts and the formation of both gender characteristics is heavenly dependent on the nutrition (Souri and Hatamian 2019). Although each phase reacts to nutrient stress differently leading to decrease in net production. However, any stress during the productive stage (Zhang et al. 2018a;) has substantial implications since productive parts are essential elements of yield and the primary source of nutrition for the whole human population (Souri and Hatamian 2019; Muhammad et al. 2022; Wiqar et al. 2022; Farhat et al. 2022; Niaz et al. 2022; Ihsan et al. 2022; Chao et al. 2022, Qin et al. 2022; Xue et al. 2022; Ali et al. 2022; Mehmood et al. 2022; El Sabagh et al. 2022; Ibad et al. 2022).
Reactive oxygen species have a detrimental effect on cellular metabolic processes and harm all biological components (Nieves-Cordones et al. 2019). Therefore, it is crucial to detoxify these reactive oxygen species, and plants have evolved extensive defenses against them (Hasanuzzaman et al. 2018a; Fahad and Bano 2012; Fahad et al. 2013, 2014a, b, 2015a, b, 2016a, b, c, d, 2017, 2018a, b, 2019a, b, 2020, 2021a, b, c, d, e, f, 2022a, b). Plant cells often increase the action of reactive oxygen species sifting enzymes and boost their creation of anti-oxidants in response to elevated reactive oxygen species levels in order to maintain redox equilibrium (Mittler et al. 2022).
Different management practice is being used to combat the different kind of stresses (Saud et al. 2013, 2014, 2016, 2017, 2020, 2022a, b). Biochar a carbon-based solid created through the burning of organic substances, including wood, animal dung, poultry manure, and municipal sludge (Amoakwah et al. 2020; Adnan et al. 2018a, b, 2019, 2020). It is sometimes referred to as burned biomass or black carbon. Controlling plant nutrition can help plants become more resilient to other different kind of environmental stresses (Fig. 8.1). The discovery and breeding of nutrient stress tolerant cultivars are now being worked on with better root architecture (Campobenedetto et al. 2021). One of these uses is utilizing a soil conditioner like biochar to shield plants from the harm caused by salt stress (Ameur et al. 2018).
2 Biochar to Alleviate Nutrient Stress
In the current climate change era, poor crop productivity has been obstructed due to unexpected seasonal climatic variations such as decreased precipitation/intense precipitation for short period, a length dry period, a short duration increases in moisture, frequent thunder storm and abrupt increase in temperature. These issues are very much challenging for agriculture in arid and semi-arid regions (Hasanuzzaman et al. 2018a). It is not possible to stop these challenges but can be managed and their destructive effects on the crops can be minimizes. Nowadays, a serious issue of nutrients stress tolerance is seen in Pakistan and around the globe. Althoufh scientist are working on it but it takes time. The plants show different kind of responses against the nutrient stress in different environmental conditions. But, all kind of plants show multiple biological responses such as production of reactive oxygen species. All the plant species can easily manage reactive active species in their systems but they require the proper dose of all nutrients.
Processed carbonous material can sustain for longer period of time as compared to non-processed organic material in arid and semi-arid climate where high temperature always burned the organic matter (Dalal and Carter 2019) resulting into to no addition of organic masses into the soil systems. Therefore, plant-based materials such as biochar is an integrated approach for soil fertility management under environment-based nutrient stress which may help achieve sustainable agricultural outputs; nevertheless, these methods require significant land modification and financial commitment (Fig. 8.2). Such kind of organic amendments has been widely used in many developed but least in developing countries which are revitalizing the nutrient deficiency in all kind of soils. Additionally, producing biochar from organic waste is an economical way to recycle the agricultural waste materials (Dai et al. 2016).
Burning agricultural waste significantly negatively affects the environment because it produces carbon dioxide, the main greenhouse gas generated by human activities. To overcome the drawbacks of direct burning, it has been proposed to carbonize woody wastes to produce biochar, a material like charcoal. Due to its resistance to biological deterioration, biochar's acoustic impacts may last far longer in terrestrial settings than compost or plant leftovers. Carbonization by pyrolysis to generate biochar is a useful technology to reduce negative impacts on environmental and health. Global warming is lessened by a dark material called biochar, which includes refractory organic carbon. High solubility of water and nutrient could be a reason of biochar addition to soil as a soil conditioner to increase soil nutrient content (Da Silva Mendes et al. 2021). Furthermore, biochar increases pH, cation exchange capacity, organic carbon, and nutrient content in soils while reducing carbon dioxide emissions. Thus, the soil amendments should be an alternative and short-term solution for sustainable nutrients under the nutrient stress (Clough et al. 2013; Chintala 2014; De Jesus Duarte et al. 2019; DeLuca and Gao 2019).
3 Nutrients Stress and Plant Growth
In order to maintain cell sustainablity and ensure life under the nutrient stress, plants have developed several adaptive/resistance mechanisms. Sever nutrient stress disturbs the flexibility of membrane lipids, which might alter the structure of the membrane (Peng et al. 2019b). By sifting reactive oxygen species produced under nutrient stress, nitrogen oxides may serve as an antioxidant and defend plants against stress (Rai 2022). According to several prior studies, nitrogen oxide signals to development of thermotolerance in plants by activating enzymes that use oxygen (Hasanuzzaman et al. 2018b; Ahmed et al. 2020; Li et al. 2020b; Fonseca-García et al. 2021). Moreover, enhancing a plant's ability to withstand environmental shocks requires proper nourishment for the plant (Adetunji et al. 2020). Similarly, potassium is crucial for agricultural plants to survive under challenging environmental conditions (Kong et al. 2020). It can improve the process of photosynthesis, turgidity maintenance and stress-induced enzyme activation under nutrient stress (Saghaiesh and Souri 2018). In most of cases, the potassium stress may hamper the carbon dioxide fixation, cell ion channels and cell wall permeability (Zhang et al. 2018b). Such turbulences lead to an excess of photosynthesis-generated electrons, which increases electron transport to oxygen and subsequently stimulates reactive oxygen species production (Kong et al. 2020). The sustainable transport of photosynthetic electrons transportation is heavenly disturbed during the nutrient deficiency because it causes oxygen to be converted to reactive oxygen species (Nieves-Cordones et al. 2019). Sometime, the cell sustainablity may be shielded against oxidative damage brought on by nutrient signalling in low potassium soil media (Wu et al. 2018). However, increasing the potassium concentration of irrigation water significantly protected the cell and its function.
4 Nutrient Stress and Plant Cell Functions
In order to achieve the necessary gains in food production, it is predicted that fertilizer use will need to double over the next 20 years (Fischer and Connor 2018). In order to increase crop production and maintain soil fertility, research on plant nutrition looks to be a top priority in the future decades (Hackman et al. 2022). To survive and produce when faced with environmental obstacles, crop plants must develop adaptive mechanisms to prevent or minimize nutrient stress (Ahmed et al. 2020). Phosphorus is required for strength generation, magnesium and nitrogen are structural components of chlorophyll that are necessary for photosynthesis while potassium is necessary for osmotic control and enzyme activation, and phosphorus is a structural part of essential plant compounds (de Souza Osório et al. 2020). Therefore, a plant that receives enough nutrition should produce more smooth and sustainable growth (Sung et al. 2018). Moreover, the hydraulic conductivity of the cortical root cells was much lower in plants that were nitrogen and phosphorous deficient (Praveen and Gupta 2018). In addition, availability of proper plant nutrient concentration are crucial to increase the water use efficiency and nutrient use efficiency enhancement of the crops (El-Nakhel et al. 2019).
Numerous studies have shown the sufficient availability of different kind of nutrients may help the plant in reducing the effects of different abiotic stressors. For example, silicon and potassium have been shown to boost tolerance of wheat crop against nutrient and salt stress (Sales et al. 2021). Nitrogen deficiency reduce the plant ability to tolerate the different kind of stresses i.e. cold, heat and salinity stresses (Ahmed et al. 2020). In addition, these stresses impaired impair plant growth and nutrient uptake. The suitable concentration of nitrogen may trigger the light harvesting and hence accelerate the process of photosynthesis (Ahmed et al. 2020). So that is why, health plant growth and yield could be achieved. Sometime, the surplus of unused light energy is anticipated in nitrogen deficient leaves, increasing the likelihood of photo-oxidative damage (Rai 2022). Similarly, a lack of nitrogen in rice plants exposed to intense light is associated with increased lipid peroxidation in the cell system (Yoo et al. 2018).
The role of sun energy in electron movement during kelvin was greater in nitrogen sufficient crops compared to nitrogen-deficient crops (Bloch et al. 2020). Additionally, nitrogen deficient plants may withstand high levels of photosynthetic activity and the production of defensive mechanisms (Rai 2022). To protect against photo-oxidative damage caused by excessive light, the thylakoid membrane provides an additional energy release mechanism, which releases heat (Manoj et al. 2020). However, in nitrogen-deficient plants, the generation of zeaxanthin and the conversion of xanthophyll cycle pigments increased, decreasing the chlorophyll concentration (Gebregziabher et al. 2021). Compared to nitrogen adequate spinach plants, nitrogen deficient spinach plants lose up to 64 percent more of the light energy that is absorbed (Moriwaki et al. 2019). This gap was attributed to alterations in the xanthophyll cycle pigments, with zeaxanthin and antheraxanthin accounting for around 65% of total xanthophyll pigments in plants havening less nitrogen (Moriwaki et al. 2019). Similarly, the use of captivated sun energy in carbon dioxide fixation is decreased in nitrogen deficient plants, leading to a more significant need for protection against excessive light energy (Prescott et al. 2020). As a method of releasing excess light energy, it was discovered that bean leaves provided with nitrate converted violaxanthin to zeaxanthin more strongly than those supplied with ammonium (Holzmann et al. 2022). Similarly, the bean plants grown in nitrate were more resistant to photodamage than bean plants grown in ammonium (Posso et al. 2020). Ammonium-grown plants showed greater lipid peroxidation levels and antioxidative enzymes due to the increased light intensity (Fonseca-García et al. 2021).
5 Physiological Alteration and Role of Micronutrients Under Nutrient Stress
Different element had different function inside the plant body and the deficiency of any other them may halt the numerous physiological processes and require for serval co-factors and enzymes of metabolism (Janpen et al. 2019). Moreover, some elements play their role at the earlier stage of plant growth and some require at the grain filling and ripening of crop. Plants are unable to complete their life cycle successfully without availability of specific elements (Zhou et al. 2021). Generally, macro-element is available to plants but they do not have micro-elements which are equally important for plant health active. Acute nutrient (micro-nutrient) stress directly harms plants by causing protein denaturation and aggregation and increased membrane lipid fluidity. The balance presence of different elements is very vital and sometime their antagonistic effect may lead to abnormal growth. Therefore, it may induce different changes in the biosynthesis of different compounds and structural components.
Such nutrients stress for longer period can lead to over production and accumulation of reactive oxygen species that could had toxic effect to nucleic acids, metabolites, proteins, and lipids of plant cells (Ogden et al. 2018). Most common ROS that plants produce under the nutrient stress including singlet oxygen, superoxide anion, and hydrogen peroxide which are generated in to all cell organelles i.e., mitochondria, peroxisomes, and chloroplast (Kim et al. 2021). However, the maintaining of some specific physiological level of reactive oxygen species is a matter of life and death for the aerobic living organism otherwise leading to death within a few hours. The proper concentration of different types of micronutrients helps the plant cell to produce the antioxidant defensive systems which is dully supported by the enzymatic and non-enzymatic compounds to tackle the harmful effects of reactive oxygen species (Nadeem and Farooq 2019).
Calcium ion is a vital ubiquitous intracellular messenger, which play a lead role in several signal cell trans transduction pathways. Moreover, the transient perturbations such as free cytosolic calcium are indispensable and translate the cell signals into various biological responses. The increase in cytosolic calcium levels resulted into higher production of calcium sensor relay proteins such as calmodulin that is called calcium biding proteins. calmodulin regulated the several transcription factors which involved in many physiological, bio-chemical, and molecular functions in the cell. Some time, cytosolic calcium activates the calmodulin-binding transcription activator which is major contributor of transcription factors. Moreover, calcium is thought to be essential for healing from stress free because it promotes the cellular membranes protein adenosine triphosphatase, which is required to transport back nutrients depleted during cell damage. calcium modulates the pressure throughout freezing damage, repair work, and cold tolerance adaptation (Pathak et al. 2020). Moreover, it also fastens the process of repairing of the damage cells and it is observed that it also enhances the tolerance against the freezing injury (Thor and Kathrin 2019; Zhang et al. 2020). In addition, it stimulates the adenosine triphosphatase enzymes which help the cell wall to recover aggressively in cold damage by mobilizing the available cell resources. Calcium is also an important element in maintaining cell structure and cell integrity (Zhang et al. 2020).
Through several physiological and biochemical processes, magnesium influences plant growth phase (Pickering et al. 2020). It is necessary for several metabolic processes, including photosynthesis (Xie et al. 2021). Even slight variations in magnesium levels significantly affect numerous necessary chloroplast enzymes (Peng et al. 2019a). Both a magnesium shortage and an excess are harmful to plant photosynthesis (Veronese et al. 2020). However, the rate of photosynthesis is noticeably decreased in the leaves of magnesium deficient plants. The nutrient stress causes several metabolic pathways in various cellular compartments, such as chloroplast, mitochondria, and peroxisomes, to continuously produce reactive oxygen species. Mineral nutrient deficit stress includes oxidative stress (Zhang et al. 2019). In addition, magnesium increased the content of antioxidant molecules and the activity of antioxidant enzymes in bean (Torabian et al. 2018), maize (Iqbal et al. 2020), wheat (Tian et al. 2021), rice (Ahmed et al. 2021) and pepper (Zirek and Ozlem 2020).
Additionally, plants lacking in micro-nutrients such as iron, boron and magnesium which decrease the accumulation of malondialdehyde into the cell (Oustric et al. 2021). The sustainable availability of these nutrients increase the root growth and surface area that helps the plants to absorb water and nutrients from the deeper layer of soils (Ali et al. 2020). In addition, they also rise the quantity of sucrose in the leaves and improves sucrose transfer from the leaves to the roots. Sometime, they also improve phloem export to boost glucose translocation under temperature stress (high or low). Moreover, the improved feeding of micronutrients increase the photosynthetic rate leading to higher yield by maintaining chloroplast structure in Cassava plants (Busener et al. 2020). However, sometimes, protein synthesis is inhibited leading to inhibition and membrane integrity is lost due to higher level of deficiency.
6 Management of Nutrient Stress
Traditional agriculture has been replaced by intensive crop cultivation due to food demand and supply (Garnier et al. 2019). Intensive (or tiring) agricultural farming has reduced the availability of plant nutrients, which harms plant protentional badly (El-Nakhel et al. 2019). Healthier crop nutrition may help plants become more resilient to different kind of stresses and increase the production of antioxidant system. The anti-oxidants protect chloroplast membrane integrity, reduce photo-oxidation, scavenge reactive oxygen species, and promote photosynthesis in the plants (de Souza Osório et al. 2020). It was also seen the availability and management of healthy concentration of macro-and micronutrient may increase the chlorophyll contents (Purbajanti et al. 2019). It was worth noted that availability of nutrients can increase of generation of strong chlorophyll pigments and general plant progress in cow pea plants even under water stress (Laranjeira et al. 2021). Moreover, the sufficient concentration of potassium and calcium encourage water uptake, assisting stomata and improves the ability of plants to withstand temperature pressure by sustaining a steady temperature.
7 Sustainable Plant Growth Under a Stressed Environment with Biochar
The rosehip seeds biochar applied at the rate of 2% (200 gram per pot) improved the shoot dry weight of sugar beet (29.82 gram per plant) under drought stress condition as compared to control (with no biochar treatment) (Durukan et al. 2020). Due to typical nature of biochar towards the binding of various micro and macro-nutrients on its charged sites due its electrostatic attractions, can increase the biding of water particles and thus decrease the frequency of irrigation and plant may save the plants from drought susceptibility (Khan et al. 2021). In addition, under nutrition stress environment, comparative higher surface area and porous structure of biochar that increase its adhesive and cohesive forces with the water and nutrients in the soils may result into slow release and gradual availability of nutrients and water to plants (Kätterer et al. 2019; Abideen et al. 2020). It was also noted that the functional groups especially oxygen related functional groups help the biochar to conserve more water molecules and plant may use in stressed environment (Suliman et al. 2017).
Enough Biochar addition to plants can elevate the stresses on stomatal conductance transpiration, photosynthesis, respiration, and turgor pressure by improving the nutrient and water availability (Phillips et al. 2020). The addition of biochar (600 °C) at rate of 2% increase the biomass (shoot and root) of licorice by 80% and 40% under the saline environment (50 mM NaCl). In addition, it also improved the root architectural characteristics such as root surface area, root length, root volume, project area and nodulation (Egamberdieva et al. 2021). Moreover, in alternate root-zone drying irrigation, overall growth (plant height and shoot biomass) and yield (grain yield) of quinoa by 11.7%, 18.8 and 10.2 % respectively compared to deficient irrigation (Yang et al. 2020). During the growth period of quinoa, it was noted that the water use efficiency, stomatal conductance and leaf photosynthetic rate and leaf Abscisic acid was also improved under the saline stress conditions as compared to non-saline environment (Yang et al. 2020).
Acceleration of nutrient cycling and carbon sequestration in the upper soil layer (0–15 cm) was achieved in the rice straw biochar treatments and improved the reduced the soil bulk density and increase the availability of nutrients. Ultimately, this phenomenon was enhanced vegetative biomass and yield (Wu et al. 2021). Similarly, the microbiome population in the soil reduced the production of reactive oxygen species under nutrients stress and improved the carbon stock leading to better nutrient availability to plants (Tang et al. 2020). Stress tolerance with biochar are associated with the release of considerable concentration of micro-nutrients (carbon, nitrogen, phosphorus, and potassium) and macro-nutrients (calcium, manganese, iron, zinc, coper) (Abd El-Mageed et al. 2020). In addition to earlier reports, positive effects of biochar materials were noted on the plant growth and development. But it was concomitant with the release of essential soil nutrients such as nitrogen, potassium, calcium and magnesium into the soil media (Zhao et al. 2020).
8 Physiochemical Changes in Soil After Biochar Addition
The physiochemical properties of all kind of soils play vital role towards the alleviation of nutritional stress and availability of nutrients. Hence, biochar is magical material which had the ability to enhance the plant growth and improve the soil health (Sattar et al. 2020). Biochar had the ability to play magical role even in nutritionally dead soil (Minhas et al. 2020). Generally, it can change the pH, cation exchange capacity, electrical conductivity, inherent nutritional capacity, electrical conductivity, solubilization ability and hence, improve the access of plant to nutrients into the soil media (Zhu et al. 2020). Biochar had the ability to clean the soils from different organic and inorganic pollutants which are increasing the soils after the haphazard application of chemicals to agricultural crops (El-Naggar et al. 2020; Khalid et al. 2020). Moreover, the leaching of fertilizers and runoff of soil is very common phenomenon in the arid and semi-arid areas. It reduces the efficiency and loss of outputs and other hand its polluting the fresh water resource. Hence, continuous and repeated application of biochar not only reduce the runoff and leaching but also sustaining the soil productivity (Ippolito et al. 2020).
Biochar application into the soil increase the soil moisture and resistant to microbial degradation which slows down the degradation process (may decrease to 0.3% per year) leading to long term sustainable availability of nutrients and accelerated the process of carbon sequestration in the arid climate (Papageorgiou et al. 2021). It was worth noted that the activities of proteases, acid phosphomonoesterases and soil fluorescein diacetate hydrolase was improved under the saline condition by the addition of biochar (600 °C) at rate of 2% under the saline conditions (50 mM NaCl) (Egamberdieva et al. 2021).
Significant concentration of some minerals i.e., magnesium, iron, and calcium and inorganic carbonates has been increased after the application of biochar into soil that improved the plant growth and development. In addition, soil carbon contents, soil permeability and soil productivity were also improved when was observed during the crop growing period and at harvest (Antala et al. 2019; Leng et al. 2019). Moreover, the biochar stimulate the microbial activities in the rhizosphere that increase the yield by improve the soil nutrients availability and soil water contents (Zhu et al. 2017). The soil porosity and cation exchange capacity was also enhanced but it was more prominent in the clay soils as compared to sandy and silt soils (Nguyen et al. 2017). Due to change in electrostatic charges of soil, it increase the release and retention of nutrients in soils, improving the plant nutrient use efficiency resulting to higher plant yield (Akhtar et al. 2014).
Addition of biochar could initiate and accelerate the process of different biochemical and enzymatic activities in the soil. Initially, the soil microbial abundance and activities has been started and provided the food to all kind of soil biota. Furthermore, they may coordinate and fasten the nutrients cycling process (Liu et al. 2017). Many nutrients solubilizing microbes like Bacillus mucilaginosus, Bacillus edaphicus and Azotobacter chroococcum may starts their actives from sluggishness due to unavailability of nutrition (Rahimzadeh et al. 2015). They mineralize the fix/Nex/chelate nutrients into solution form. The activities of some Bacillus species could be promoted by 5-fold when they are incubated with biochar of corn stover (0.6%). The nutrients release activities of soil is increased by 80% (Liu et al. 2017). It has been worth noted that application of B. mucilaginosus into mica rich soil boost up the growth and development of lemon grass. This could be due to more mobilization of the potassium from the available resources of mica (Basak et al. 2021) (Fig. 8.3).
9 Management of Nutrients by Biochar Under Nutritional Stress
The biochar had the ability to mitigate numerous environmental stresses such as drought, salinity, heavy metals, nutritional stress, heat stress, climate change effects and pollution effects etc. from the plants. Usually, it was noted that all plants accumulates ethylene under the stresses including the nutritional stress (Khan et al. 2015). That production of ethylene under stress condition is high dangerous to plant cell and starting its damage from degradation of cell membrane lapis of chloroplast and then further activates the chlorophyllase gene (chlase) (Michaud and Jouhet 2019). The chlorophyllase may lead to degradation of chlorophyll and finally chlorosis may result. Biochar could slow down the process of ethylene production by providing of nutrients through its slow-release mechanism. Thus, a large number researcher reported that biochar could eliminate the nutrient stress in all kind of soils (Wacal et al. 2019; Chen et al. 2022; Shaheen et al. 2022).
Biochar is generated from biomass that has been paralyzed in a low-oxygen environment and is a fine-grained charcoal with a high concentration of refractory organic carbon (Lehmann and Joseph 2015; Amoakwah et al. 2020). Its application in agricultural soils to capture carbon, enhance soil functioning, and other purposes has been hotly contested (Lehmann 2007). Carbon-rich biochar may increase soil fertility by enhancing the ability of soil to retain nutrients. All the crop nutritionist suggested that carbon-rich biochar is the game changer to enhance the soil fertility of poor soil in the arid and semi-arid climate. Moreover, the structure of carbon based material is aromatic which give it a lot of characteristics like low density, large surface area, high ion exchange capability, and great porosity which make it more resistive to disintegration (Agegnehu et al. 2017). The material and pore volume of carbon-based material can greatly enhance the physical and chemical properties of soil, which are essential for soil cooling and crop production. These properties include water retention, hydraulic properties, aggregate stability, pH, organic carbon, and cation exchange capacity (Dai et al. 2016; Baiamonte et al. 2019). Moreover, the physical properties of soil has been improved because of presence of micropores and less density of carbon based particles (Lehmann et al. 2011). Additionally, the presence of nitrogen in biochar may alter the dynamics of soil nitrogen by influencing the quantity of soil nitrogen that is available to plants, and it increases its ability to absorb more nitrogen, and accelerate the biological processes of nitrification (Ameur et al. 2018; Amoakwah et al. 2020).
Moreover, by enhancing the physical environment of the soil, which prevents or lowers anaerobic denitrification, carbon dioxide flow, and methane gas generation, applying biochar to soil may also reduce greenhouse gas emission (Ali et al. 2017). Additionally, adding biochar to field improves infiltration and water-holding capacity, particularly in soils with a coarse texture or a high concentration of macrospores (Agegnehu et al. 2017). Biochar contains different amounts of nitrogen and carbon depending on its feedstock and production conditions and its additives sequester more carbon and nutrients in the soil because of their promotive properties. The natural ability of biochar in controlling nutrients uptake that is ultimately reduces the reactive oxygen species and abscisic acid in the cabbage seedlings. Under the nutrients stress conditions, biochar was effective at reducing Nitrate (NO3), Ammonium (NH4+), phosphate (PO4 3-), potassium (K+), calcium (Ca2+), and magnesium (Mg2+) (Gao and DeLuca 2018). In addition, it is worth noted that potassium leaching is significantly reduced with the addition of biochar.
Physical and chemical soil factors such as, water-holding capacity, cation exchange capacity, pH, surface area, porosity, bulk density, carbon, nitrogen, nitrogen used efficiency, and total accessible nitrogen and phosphorus are between the physical and chemical soil parameters that biochar affects. It was noted that majority of macro and micro-nutrients such as hydrogen, oxygen, magnesium, and macronutrients including nitrogen, phosphorus, and potassium are all present in biochar and can help most crops throughout the globe grow more quickly. It was seen the biochar increased the nitrogen retention efficiency that in return decrease the use of synthetic fertilizer to the crops. Upon the addition of maize residue biochar at the rate of 1–2% (weight/weight), the amount of total nitrogen increased by 41%, the amount of accessible P by 165%, the amount of available potassium by 160% (Saffari et al. 2020). In addition, Adekiya et al. (2020) recorded that soils that have amendment of biochar had higher levels of essential nutrients.
Biochar improved the nitrogen concentration in the stem, root, fruits, and leaves under the normal and stress conditions as compared to control treatments (no biochar). Under drought stress condition, the rosehip seeds biochar applied at the rate of 2% (200 gram per plant) increased the nitrogen concertation at 1.72% as compared to control treatments (no biochar) (Park et al. 2019; Durukan et al. 2020). Moreover, the electrostatic attraction among the various micro and macro-nutrients and the charges sites of biochar may increase the concentration of ammonium and nitrate ions. However, this higher release of ammonium ions was seen when the biochar was produced at low temperature (400–500 °C) (Xu et al. 2019; Zhou et al. 2019).
Biochar can alter the amount of accessible phosphorus in soil in solution form to plants and prevent its fixation and sorption on the clay minerals (Uchimiya et al. 2015; Zhao et al. 2016). Moreover, biochar could help the farmers of poor and developing countries in increase the soil phosphorous use efficiency and reducing the phosphorus losses due to its ability of slow releasing of nutrients. Hence, it may work as phosphorus fertilizers for future generations and could increase phosphorus use efficiency for longer term especially in nutrient deficient period (Li et al. 2020a). The success stories of its residual effects on crop growth and development are also confirmed. Due to different surface properties like as basic, acidic, heterogeneous a and hydrophilic characteristics, biochar can increase solubility and availability of phosphorus under the various climatic conditions (Trazzi et al. 2016; Glaser and Lehr 2019). The rosehip seeds biochar applied at the rate of 0.5% (50 gram per plant) increased the nitrogen concertation at 1.01% as compared to control treatments (no biochar) (Durukan et al. 2020).
Soil potassium is divided into four types basis on its availability such as exchangeable/soluble potassium, non-exchangeable potassium, water-soluble potassium, and mineral potassium. All these potassium fate into the soil systems is in dynamic equilibrium and play vital role for its availability and update into the plant system (He et al. 2015). Although the potassium reserves are large in the soil system of arid and semi-arid system of the globe but are in non-exchangeable potassium form. However, application of biochar at different rates was significantly increased the proportion of exchangeable potassium into the soil media that is readily available to plant rooting system from the longer period. In addition, some time, potassium is present in mineral potassium or exchangeable potassium forms that is sparingly or partial available in the rhizosphere (Oram et al. 2014). A lot of research question are still unexplored regarding to interaction of biochar time/amount and potassium or biochar application and type of clay minerals. Moreover, the specific interactions and process between the biochar application timing and its interaction with the soil components and the processes involved in it. Moreover, the rosehip seeds biochar applied at the rate of 2% (200 gram per plant) increased the potassium concertation at 2.33% as compared to control treatments (no biochar) (Durukan et al. 2020).
On the other hand, potassium is conserved during the biochar production process and easily available in the form of potassium containing salt having high solubility but its ability is heavenly dependent on the input material from which it is produced. So, that is why, several past studies indicated that potential source of potassium in the form of biochar could be a chief substitute of conventional and synthetic fertilizers. Some studies exhibited that quick release of potassium may result into unavailability of potassium after first year but non the other hand, it was noted in the previous studies that role of soil properties such as including soil texture, type, pH, inherent potassium-reserves, and concentration of clay minerals is determined the dynamic of potassium into the soil and rhizosphere.
The rosehip seeds biochar applied at the rate of 2% (200 gram per plant) was improved the micro-nutrient concentration (magnesium and manganese) in the stem of sugar beet (Durukan et al. 2020). The electrostatic attraction among the opposite charges ions may increase the concentration of many micro-nutrients such as calcium, iron and magnesium etc. (Chandra et al. 2020). In addition, biochar helps the soil media to release the significant concentration of fixed micro-nutrients such as manages, iron, calcium, copper, and zinc. Hence more concentration these micro-nutrients was noted in the plant body (Abd El-Mageed et al. 2020). In long run, the application of handful amount of biochar into soil may reduce the need of synthetic fertilizers and pesticides because it can improve the concentration of micro-nutrients, organic matter, soil carbon concertation, nutrients cycling, soil enzymes activities, soil fertility and soil microbial activities leading to achieve the sustainablity and profitability of the farming community (Abd El-Mageed et al. 2020).
It was seen the under nutrient stress, the addition of biochar to the crop may correct the imbalance concentration of calcium, iron, zinc, and sulfur etc. that are vital from plant growth and development (Mwando et al. 2020). Moreover, biochar plays vital role in improving the human and animal nutritional status that are heavenly dependent on the plants for its nutrition. Generally, it was observed that micro-nutrients (magnesium, calcium and manganese) was fixed into the soil particles but was easily released into soil system in long term field experiments when biochar (corn straw biochar) was added to soil before the seed sowing (Zhao et al. 2020).
10 Conclusion
Nutrient-nutrient interconnection and responses and further its impact on ions accumulation into the cell are well explored. However, the nutrient based cell signalling is still a topic to debate. Such signal may deceive the cell other signal. So, it may disturb the cell routine activities. How all the terrestrial plants crop with poor nutritional acquisition in soil is an interesting question in biology. Now a days, nutrient stress along with climate change challenges which plants are facing in nature. That is why, sudden changes in growth capacity of plants can be seen due to abrupt changes in ion homeostasis interactions with in plant cell system (Fig. 8.4).
The combinatorial signal mechanism among the different cell of the plant under the nutrient stress yet to be focused in the future research program. Moreover, there is dire need to improve the plant genetic system to tackle the combined stresses and it may lead to development of plant species with better genetic architectures that may handle each individual stress response. Therefore, future research program should be designed to exploring the answer the question of how the nutrient homeostasis in plant body push the plant to change its genetic architecture and how it identifies the effect of the combination of different nutrient stress on a single plant in the field condition. Moreover, the lack of research of the role of molecular mechanism of integrated nutrient stressed cell signals for the development process of cell is the demand of the current era. Similarly, the use of 3D network modelling could be a handy tool to understand and predict the ionome for any combination of nutrients for any specific genotype at the given time and space. The interaction of different nutrients stress singles with ionome and growth and how they change the different mechanism pathways in the cell that may re-regulate ion homeostasis and plant development. Sometimes, such signals deceive the plant systems with immune signaling pathways that produces different chemicals into the soil. These chemicals are very necessary to cohabitate plants with soils to manage the limited nutrients in the soil system. This interconnection between the cell signalling and immunity needs a lot of attention of plant researchers. Therefore, cellular level improvement is needed to cope with nutrient stress signalling system. So, any molecular mechanism improvement that may help the plant breeder to introduce the plant ideotypes. It will be a game changer in precision farming era and ensure the food security in the climate change scenarios.
References
Abd El-Mageed TA, Rady MM, Taha RS, Abd El Azeam S, Simpson CR, Semida WM (2020) Effects of integrated use of residual sulfur-enhanced biochar with effective microorganisms on soil properties, plant growth and short-term productivity of Capsicum annuum under salt stress. Sci Hortic 261:108930. https://doi.org/10.1016/j.scienta.2019.108930
Abid M, Khalid N, Qasim A, Saud A, Manzer HS, Chao W, Depeng W, Shah S, Jan B, Subhan D, Rahul D, Hafiz MH, Wajid N, Muhammad M, Farooq S, Fahad S (2021) Exploring the potential of moringa leaf extract as bio stimulant for improving yield and quality of black cumin oil. Sci Rep 11:24217. https://doi.org/10.1038/s41598-021-03617-w
Abideen Z, Koyro HW, Huchzermeyer B, Ansari R, Zulfiqar F, Gul B (2020) Ameliorating effects of biochar on photosynthetic efficiency and antioxidant defence of Phragmites karka under drought stress. Plant Biol 22(2):259–266. https://doi.org/10.1111/plb.13054
Adekiya AO, Agbede TM, Ejue WS, Aboyeji CM, Dunsin O, Aremu CO, Owolabi AO, Ajiboye BO, Okunlola OF, Adesola OO (2020) Biochar, poultry manure and NPK fertilizer: sole and combine application effects on soil properties and ginger (Zingiber officinale Roscoe) performance in a tropical Alfisol. Open Agric 5(1):30–39. https://doi.org/10.1515/opag-2020-0004
Adetunji DA, Obideyi OA, Evinemi OT, Adetunji OA (2020) Phytotoxicity assessment of compost-type biofertilizer using co-composting and post composting fortification methods. Asian J Agric Food Sci 8(3). https://doi.org/10.24203/ajafs.v8i3.6240
Adnan M, Zahir S, Fahad S, Arif M, Mukhtar A, Imtiaz AK, Ishaq AM, Abdul B, Hidayat U, Muhammad A, Inayat-Ur R, Saud S, Muhammad ZI, Yousaf J, Amanullah HMH, Wajid N (2018a) Phosphate-solubilizing bacteria nullify the antagonistic effect of soil calcification on bioavailability of phosphorus in alkaline soils. Sci Rep 8:4339. https://doi.org/10.1038/s41598-018-22653-7
Adnan M, Shah Z, Sharif M, Rahman H (2018b) Liming induces carbon dioxide (CO2) emission in PSB inoculated alkaline soil supplemented with different phosphorus sources. Environ Sci Pollut Res 25(10):9501–9509. https://doi.org/10.1007/s11356-018-1255-4
Adnan M, Fahad S, Khan IA, Saeed M, Ihsan MZ, Saud S, Riaz M, Wang D, Wu C (2019) Integration of poultry manure and phosphate solubilizing bacteria improved availability of Ca bound P in calcareous soils. 3 Biotech 9(10):368. https://doi.org/10.1007/s13205-019-1894-2
Adnan M, Fahad S, Muhammad Z, Shahen S, Ishaq AM, Subhan D, Zafar-ul-Hye M, Martin LB, Raja MMN, Beena S, Saud S, Imran A, Zhen Y, Martin B, Jiri H, Rahul D (2020) Coupling phosphate-solubilizing bacteria with phosphorus supplements improve maize phosphorus acquisition and growth under lime induced salinity stress. Plants 9(900). https://doi.org/10.3390/plants9070900
Agegnehu G, Srivastava AK, Bird MI (2017) The role of biochar and biochar-compost in improving soil quality and crop performance: a review. Appl Soil Ecol 119:156–170. https://doi.org/10.1016/j.apsoil.2017.06.008
Ahmad N, Hussain S, Ali MA, Minhas A, Waheed W, Danish S, Fahad S, Ghafoor U, Baig KS, Sultan H, Muhammad IH, Mohammad JA, Theodore DM (2022) Correlation of soil characteristics and citrus leaf nutrients contents in current scenario of layyah district. Hortic 8:61. https://doi.org/10.3390/horticulturae8010061
Ahmed M, Hasanuzzaman M, Raza MA, Malik A, Ahmad S (2020) Plant nutrients for crop growth, development and stress tolerance. In: Sustainable Agriculture in the Era of Climate Change. Springer, pp 43–92. https://doi.org/10.1007/978-3-030-45669-6_3
Ahmed T, Noman M, Manzoor N, Shahid M, Hussaini KM, Rizwan M, Ali S, Maqsood A, Li B (2021) Green magnesium oxide nanoparticles-based modulation of cellular oxidative repair mechanisms to reduce arsenic uptake and translocation in rice (Oryza sativa L.) plants. Environ Pollut 288:117785. https://doi.org/10.1016/j.envpol.2021.117785
Akhtar SS, Li G, Andersen MN, Liu F (2014) Biochar enhances yield and quality of tomato under reduced irrigation. Agric Water Manag 138:37–44. https://doi.org/10.1016/j.agwat.2014.02.016
Ali A, Guo D, Zhang Y, Sun X, Jiang S, Guo Z, Huang H, Liang W, Li R, Zhang ZJS (2017) Using bamboo biochar with compost for the stabilization and phytotoxicity reduction of heavy metals in mine-contaminated soils of China. Sci Rep 7(1):1–12. https://doi.org/10.1038/s41598-017-03045-9
Ali A, Bhat BA, Rather GA, Malla BA, Ganie SA (2020) Proteomic studies of micronutrient deficiency and toxicity. In: Plant micronutrients. Springer, pp 257–284. https://doi.org/10.1007/978-3-030-49856-6_11
Ali S, Hameed G, Muhammad A, Depeng W, Fahad S (2022) Comparative genetic evaluation of maize inbred lines at seedling and maturity stages under drought stress. J Plant Growth Regul. https://doi.org/10.1007/s00344-022-10608-2
Al-Zahrani HS, Alharby HF, Fahad S (2022) Antioxidative defense system, hormones, and metabolite accumulation in different plant parts of two contrasting rice cultivars as influenced by plant growth regulators under heat stress. Front Plant Sci 13:911846. https://doi.org/10.3389/fpls.2022.911846
Ameur D, Zehetner F, Johnen S, Jöchlinger L, Pardeller G, Wimmer B, Rosner F, Faber F, Dersch G, Zechmeister-Boltenstern S, Mentler A, Soja G, Keiblinger KM (2018) Activated biochar alters activities of carbon and nitrogen acquiring soil enzymes. Pedobiologia 69:1–10. https://doi.org/10.1016/j.pedobi.2018.06.001
Amjad SF, Mansoora N, Din IU, Khalid IR, Jatoi GH, Murtaza G, Yaseen S, Naz M, Danish S, Fahad S et al (2021) Application of zinc fertilizer and mycorrhizal inoculation on physio- biochemical parameters of wheat grown under water-stressed environment. Sustainability 13:11007. https://doi.org/10.3390/su131911007
Amoakwah E, Arthur E, Frimpong KA, Parikh SJ, Islam R (2020) Soil organic carbon storage and quality are impacted by corn cob biochar application on a tropical sandy loam. J Soil Sediment 20(4):1960–1969. https://doi.org/10.1007/s11368-019-02547-5
Amsili JP, van Es HM, Schindelbeck RR (2021) Cropping system and soil texture shape soil health outcomes and scoring functions. Soil Security 4:100012. https://doi.org/10.1016/j.soisec.2021.100012
Anam I, Huma G, Ali H, Muhammad K, Muhammad R, Aasma P, Muhammad SC, Noman W, Sana F, Sobia A, Fahad S (2021) Ameliorative mechanisms of turmeric-extracted curcumin on arsenic (As)-induced biochemical alterations, oxidative damage, and impaired organ functions in rats. Environ Sci Pollut Res. https://doi.org/10.1007/s11356-021-15695-4
Antala M, Sytar O, Rastogi A, Brestic M (2019) Potential of karrikins as novel plant growth regulators in agriculture. Plants 9(1):43. https://doi.org/10.3390/plants9010043
Baiamonte G, Crescimanno G, Parrino F, De-Pasquale C (2019) Effect of biochar on the physical and structural properties of a desert sandy soil. Catena 175:294–303. https://doi.org/10.1016/j.catena.2018.12.019
Basak BB, Saha A, Sarkar B, Kumar BP, Gajbhiye NA, Banerjee A (2021) Repurposing distillation waste biomass and low-value mineral resources through biochar-mineral-complex for sustainable production of high-value medicinal plants and soil quality improvement. Sci Total Environ 760:143319. https://doi.org/10.1016/j.scitotenv.2020.143319
Bechtaoui N, Rabiu MK, Raklami A, Oufdou K, Hafidi M, Jemo M (2021) Phosphate-dependent regulation of growth and stresses management in plants. Front Plant Sci 12. https://doi.org/10.3389/fpls.2021.679916
Bloch SE, Ryu M-H, Ozaydin B, Broglie R (2020) Harnessing atmospheric nitrogen for cereal crop production. Curr Opin Biotechnol 62:181–188. https://doi.org/10.1016/j.copbio.2019.09.024
Borysiuk K, Ostaszewska-Bugajska M, Kryzheuskaya K, Gardeström P, Szal B (2022) Glyoxalase I activity affects Arabidopsis sensitivity to ammonium nutrition. Plant Cell Rep 4:1–21. https://doi.org/10.1007/s00299-022-02931-5
Bukhari MA, Adnan NS, Fahad S, Javaid I, Fahim N, Abdul M, Mohammad SB (2021) Screening of wheat (Triticum aestivum L.) genotypes for drought tolerance using polyethylene glycol. Arab J Geosci 14:2808. https://doi.org/10.1007/s12517-021-09073-0
Busener N, Kengkanna J, Saengwilai PJ, Bucksch A (2020) Image-based root phenotyping links root architecture to micronutrient concentration in cassava. Plant People Planet 2(6):678–687. https://doi.org/10.1002/ppp3.10130
Campobenedetto C, Mannino G, Beekwilder J, Contartese V, Karlova R, Bertea CM (2021) The application of a biostimulant based on tannins affects root architecture and improves tolerance to salinity in tomato plants. Sci Rep 11(1):1–15. https://doi.org/10.1038/s41598-020-79770-5
Chandra S, Medha I, Bhattacharya J (2020) Potassium-iron rice straw biochar composite for sorption of nitrate, phosphate, and ammonium ions in soil for timely and controlled release. Sci Total Environ 712:136337. https://doi.org/10.1016/j.scitotenv.2019.136337
Chao W, Youjin S, Beibei Q, Fahad S (2022) Effects of asymmetric heat on grain quality during the panicle initiation stage in contrasting rice genotypes. J Plant Growth Regul. https://doi.org/10.1007/s00344-022-10598-1
Chen L, Li X, Peng Y, Xiang P, Zhou Y, Yao B, Zhou Y, Sun C (2022) Co-application of biochar and organic fertilizer promotes the yield and quality of red pitaya (Hylocereus polyrhizus) by improving soil properties. Chemosphere 294:133619. https://doi.org/10.1016/j.chemosphere.2022.133619
Chintala RMJ, Schumacher TE, Malo DD, Julson JL (2014) Effect of biochar on chemical properties of acidic soil. Archive Agron Soil Sci 60:393–404. https://doi.org/10.1080/03650340.2013.789870
Clough TJ, Condron LM, Kammann C, Müller C (2013) A review of biochar and soil nitrogen dynamics. Agronomy 3(2):275–293. https://doi.org/10.3390/agronomy3020275
Crandall AK, Madhudi N, Osborne B, Carter A, Williams AK, Temple JL (2022) The effect of food insecurity and stress on delay discounting across families: a COVID-19 natural experiment. BMC Public Health 22(1):1576. https://doi.org/10.1186/s12889-022-13969-1
Da Silva Mendes J, Fernandes JD, Chaves LHG, Guerra HOC, Tito GA, de Brito CI (2021) Chemical and physical changes of soil amended with biochar. Water Air Soil Pollut 232(8):1–13. https://doi.org/10.1007/s11270-021-05289-8
Dai L, Li H, Tan F, Zhu N, He M, Hu GJGB (2016) Biochar: a potential route for recycling of phosphorus in agricultural residues. GCB Bioenergy 8(5):852–858. https://doi.org/10.1111/gcbb.12365
Dalal R, Carter J (2019) Soil organic matter dynamics and carbon sequestration in Australian tropical soils. In: Global climate change and tropical ecosystems. CRC Press, pp 283–314. https://doi.org/10.1201/9780203753187
De Jesus DS, Glaser B, Paiva de Lima R, Pelegrino C, Carlos E (2019) Chemical, physical, and hydraulic properties as affected by one year of miscanthus biochar interaction with sandy and loamy tropical soils. Soil Systems 3(2):24. https://doi.org/10.3390/soilsystems3020024
de Souza Osório CRW, Marques Teixeira GC, Barreto RF, Silva Campos CN, Freitas Leal AJ, Teodoro PE, de Mello PR (2020) Macronutrient deficiency in snap bean considering physiological, nutritional, and growth aspects. PLoS One 15(6):e0234512. https://doi.org/10.1371/journal.pone.0234512
Deepranjan S, Ardith SO, Siva D, Sonam S, Shikha MP, Amitava R, Sayyed RZ, Abdul G, Mohammad JA, Subhan D, Fahad S, Rahul D (2021) Optimizing nutrient use efficiency, productivity, energetics, and economics of red cabbage following mineral fertilization and biopriming with compatible rhizosphere microbes. Sci Rep 11:15680. https://doi.org/10.1038/s41598-021-95092-6
DeLuca TH, Gao S (2019) Use of biochar in organic farming. In: Organic farming. Springer, pp 25–49. https://doi.org/10.1038/s41598-019-45693-z
Durukan H, Demirbas A, Turkekul I (2020) Effects of biochar rates on yield and nutrient uptake of sugar beet plants grown under drought stress. Commun Soil Sci Plant Anal 51(21):2735–2745. https://doi.org/10.1080/00103624.2020.1849257
Egamberdieva D, Ma H, Alaylar B, Zoghi Z, Kistaubayeva A, Wirth S, Bellingrath-Kimura SD (2021) Biochar amendments improve licorice (Glycyrrhiza uralensis Fisch.) growth and nutrient uptake under salt stress. Plants 10(10):2135. https://doi.org/10.3390/plants10102135
EL Sabagh A, Islam MS, Hossain A, Iqbal MA, Mubeen M, Waleed M, Reginato M, Battaglia M, Ahmed S, Rehman A, Arif M, Athar H-U-R, Ratnasekera D, Danish S, Raza MA, Rajendran K, Mushtaq M, Skalicky M, Brestic M, Soufan W, Fahad S, Pandey S, Kamran M, Datta R, Abdelhamid MT (2022) Phytohormones as Growth Regulators During Abiotic Stress Tolerance in Plants. Front Agron 4:765068. https://doi.org/10.3389/fagro.2022.765068
El-Naggar A, Lee M-H, Hur J, Lee YH, Igalavithana AD, Shaheen SM, Ryu C, Rinklebe J, Tsang DC, Ok YS (2020) Biochar-induced metal immobilization and soil biogeochemical process: an integrated mechanistic approach. Sci Total Environ 698:134112. https://doi.org/10.1016/j.scitotenv.2019.134112
El-Nakhel C, Pannico A, Kyriacou MC, Giordano M, De Pascale S, Rouphael Y (2019) Macronutrient deprivation eustress elicits differential secondary metabolites in red and green-pigmented butterhead lettuce grown in a closed soilless system. J Sci Food Agric 99(15):6962–6972. https://doi.org/10.1002/jsfa.9985
Fahad S, Bano A (2012) Effect of salicylic acid on physiological and biochemical characterization of maize grown in saline area. Pak J Bot 44:1433–1438
Fahad S, Chen Y, Saud S, Wang K, Xiong D, Chen C, Wu C, Shah F, Nie L, Huang J (2013) Ultraviolet radiation effect on photosynthetic pigments, biochemical attributes, antioxidant enzyme activity and hormonal contents of wheat. J Food, Agri Environ 11(3 & 4):1635–1641
Fahad S, Hussain S, Bano A, Saud S, Hassan S, Shan D, Khan FA, Khan F, Chen Y, Wu C, Tabassum MA, Chun MX, Afzal M, Jan A, Jan MT, Huang J (2014a) Potential role of phytohormones and plant growth-promoting rhizobacteria in abiotic stresses: consequences for changing environment. Environ Sci Pollut Res 22(7):4907–4921. https://doi.org/10.1007/s11356-014-3754-2
Fahad S, Hussain S, Matloob A, Khan FA, Khaliq A, Saud S, Hassan S, Shan D, Khan F, Ullah N, Faiq M, Khan MR, Tareen AK, Khan A, Ullah A, Ullah N, Huang J (2014b) Phytohormones and plant responses to salinity stress: a review. Plant Growth Regul 75(2):391–404. https://doi.org/10.1007/s10725-014-0013-y
Fahad S, Hussain S, Saud S, Tanveer M, Bajwa AA, Hassan S, Shah AN, Ullah A, Wu C, Khan FA, Shah F, Ullah S, Chen Y, Huang J (2015a) A biochar application protects rice pollen from high-temperature stress. Plant Physiol Biochem 96:281–287. https://doi.org/10.1016/j.plaphy.2015.08.009
Fahad S, Nie L, Chen Y, Wu C, Xiong D, Saud S, Hongyan L, Cui K, Huang J (2015b) Crop plant hormones and environmental stress. Sustain Agric Rev 15:371–400. https://doi.org/10.1007/978-3-319-09132-7_10
Fahad S, Hussain S, Saud S, Hassan S, Chauhan BS, Khan F et al (2016a) Responses of rapid viscoanalyzer profile and other rice grain qualities to exogenously applied plant growth regulators under high day and high night temperatures. PLoS One 11(7):e0159590. https://doi.org/10.1371/journal.pone.0159590
Fahad S, Hussain S, Saud S, Khan F, Hassan S Jr, Nasim W, Arif M, Wang F, Huang J (2016b) Exogenously applied plant growth regulators affect heat-stressed rice pollens. J Agron Crop Sci 202:139–150. https://doi.org/10.1111/jac.12148
Fahad S, Hussain S, Saud S, Hassan S, Ihsan Z, Shah AN, Wu C, Yousaf M, Nasim W, Alharby H, Alghabari F, Huang J (2016c) Exogenously applied plant growth regulators enhance the morphophysiological growth and yield of rice under high temperature. Front Plant Sci 7:1250. https://doi.org/10.3389/fpls.2016.01250
Fahad S, Hussain S, Saud S, Hassan S, Tanveer M, Ihsan MZ, Shah AN, Ullah A, Nasrullah KF, Ullah S, Alharby HNW, Wu C, Huang J (2016d) A combined application of biochar and phosphorus alleviates heat-induced adversities on physiological, agronomical and quality attributes of rice. Plant Physiol Biochem 103:191–198. https://doi.org/10.1016/j.plaphy.2016.03.001
Fahad S, Bajwa AA, Nazir U, Anjum SA, Farooq A, Zohaib A, Sadia S, Nasim W, Adkins S, Saud S, Ihsan MZ, Alharby H, Wu C, Wang D, Huang J (2017) Crop production under drought and heat stress: plant responses and management options. Front Plant Sci 8:1147. https://doi.org/10.3389/fpls.2017.01147
Fahad S, Muhammad ZI, Abdul K, Ihsanullah D, Saud S, Saleh A, Wajid N, Muhammad A, Imtiaz AK, Chao W, Depeng W, Jianliang H (2018a) Consequences of high temperature under changing climate optima for rice pollen characteristics-concepts and perspectives. Archives Agron Soil Sci. https://doi.org/10.1080/03650340.2018.1443213
Fahad S, Abdul B, Adnan M (eds) (2018b) Global wheat production. IntechOpen United Kingdom. https://doi.org/10.5772/intechopen.72559
Fahad S, Rehman A, Shahzad B, Tanveer M, Saud S, Kamran M, Ihtisham M, Khan SU, Turan V, Rahman MHU (2019a) Rice responses and tolerance to metal/metalloid toxicity. In: Hasanuzzaman M, Fujita M, Nahar K, Biswas JK (eds) Advances in rice research for abiotic stress tolerance. Woodhead Publ Ltd, Abington Hall Abington, Cambridge CB1 6AH, Cambs, England, pp 299–312. https://doi.org/10.1016/B978-0-12-814332-2.00014-9
Fahad S, Adnan M, Hassan S, Saud S, Hussain S, Wu C, Wang D, Hakeem KR, Alharby HF, Turan V, Khan MA, Huang J (2019b) Rice responses and tolerance to high temperature. In: Hasanuzzaman M, Fujita M, Nahar K, Biswas JK (eds) Advances in rice research for abiotic stress tolerance. Woodhead Publ Ltd, Abington Hall Abington, Cambridge CB1 6AH, Cambs, England, pp 201–224. https://doi.org/10.1016/B978-0-12-814332-2.00010-1
Fahad S, Hasanuzzaman M, Alam M, Ullah H, Saeed M, Ali Khan I, Adnan M (eds) (2020) Environment, climate, plant and vegetation growth. Springer Nature Switzerland AG. https://doi.org/10.1007/978-3-030-49732-3
Fahad S, Sönmez O, Saud S, Wang D, Wu C, Adnan M, Turan V (eds) (2021a) Plant growth regulators for climate-smart agriculture, 1st edn. Footprints of climate variability on plant diversity. CRC Press, Boca Raton
Fahad S, Sonmez O, Saud S, Wang D, Wu C, Adnan M, Turan V (eds) (2021b) Climate change and plants: biodiversity, growth and interactions 1st edn. Footprints of climate variability on plant diversity. CRC Press, Boca Raton
Fahad S, Sonmez O, Saud S, Wang D Wu C, Adnan M, Turan V (eds) (2021c) Developing climate resilient crops: improving global food security and safety, 1st edn. Footprints of climate variability on plant diversity. CRC Press, Boca Raton
Fahad S, Sönmez O, Turan V, Adnan M, Saud S, Wu C, Wang D (eds) (2021d) Sustainable soil and land management and climate change, 1st edn. Footprints of climate variability on plant diversity. CRC Press, Boca Raton
Fahad S, Sönmez O, Saud S, Wang D, Wu C, Adnan M, Arif M, Amanullah (eds) (2021e) Engineering tolerance in crop plants against abiotic stress, 1st edn. Footprints of climate variability on plant diversity. CRC Press, Boca Raton
Fahad S, Saud S, Yajun C, Chao W, Depeng W (eds) (2021f) Abiotic stress in plants. IntechOpen United Kingdom, p 2021. https://doi.org/10.5772/intechopen.91549
Fahad S, Adnan M, Saud S (eds) (2022a) Improvement of plant production in the era of climate change, 1st edn. Footprints of climate variability on plant diversity. CRC Press, Boca Raton
Fahad S, Adnan M, Saud S, Nie L (eds) (2022b) Climate change and ecosystems: challenges to sustainable development, 1st edn. Footprints of climate variability on plant diversity. CRC Press, Boca Raton
Fakhre A, Ayub K, Fahad S, Sarfraz N, Niaz A, Muhammad AA, Muhammad A, Khadim D, Saud S, Shah H, Muhammad ASR, Khalid N, Muhammad A, Rahul D, Subhan D (2021) Phosphate solubilizing bacteria optimize wheat yield in mineral phosphorus applied alkaline soil. J Saudi Soc Agric Sci. https://doi.org/10.1016/j.jssas.2021.10.007
Farhat UK, Adnan AK, Kai L, Xuexuan X, Muhammad A, Fahad S, Rafiq A, Mushtaq AK, Taufiq N, Faisal Z (2022) Influences of long-term crop cultivation and fertilizer management on soil aggregates stability and fertility in the Loess Plateau, Northern China. J Soil Sci Plant Nutr. https://doi.org/10.1007/s42729-021-00744-1
Fischer R, Connor D (2018) Issues for cropping and agricultural science in the next 20 years. Field Crop Res 222:121–142. https://doi.org/10.1016/j.fcr.2018.03.008
Fonseca-García C, Nava N, Lara M, Quinto C (2021) An NADPH oxidase regulates carbon metabolism and the cell cycle during root nodule symbiosis in common bean (Phaseolus vulgaris). BMC Plant Biol 21(1):1–16. https://doi.org/10.1186/s12870-021-03060-z
Gao S, DeLuca TH (2018) Wood biochar impacts soil phosphorus dynamics and microbial communities in organically-managed croplands. Soil Biol Biochem 126:144–150. https://doi.org/10.1016/j.soilbio.2018.09.002
Garnier J, Le Noë J, Marescaux A, Sanz-Cobena A, Lassaletta L, Silvestre M, Thieu V, Billen G (2019) Long-term changes in greenhouse gas emissions from French agriculture and livestock (1852–2014): From traditional agriculture to conventional intensive systems. Sci Total Environ 660:1486–1501. https://doi.org/10.1016/j.scitotenv.2019.01.048
Gebregziabher BS, Zhang S, Qi J, Azam M, Ghosh S, Feng Y, Huai Y, Li J, Li B, Sun J (2021) Simultaneous determination of carotenoids and chlorophylls by the HPLC-UV-VIS method in soybean seeds. Agronomy 11(4):758. https://doi.org/10.3390/agronomy11040758
Glaser B, Lehr V-I (2019) Biochar effects on phosphorus availability in agricultural soils: a meta-analysis. Sci Rep 9(1):9338–9338. https://doi.org/10.1038/s41598-019-45693-z
Golden NH, Cotter EM (2021) Adolescent Nutrition. In: Reference module in biomedical sciences. Elsevier. https://doi.org/10.1016/B978-0-12-818872-9.00001-7
Hackman JJ, Rose BD, Frank HE, Vilgalys R, Cook RL, Garcia K (2022) NPK fertilizer use in loblolly pine plantations: who are we really feeding? For Ecol Manage 520:120393. https://doi.org/10.1016/j.foreco.2022.120393
Haider SA, Lalarukh I, Amjad SF, Mansoora N, Naz M, Naeem M, Bukhari SA, Shahbaz M, Ali SA, Marfo TD, Subhan D, Rahul D, Fahad S (2021) Drought stress alleviation by potassium-nitrate-containing chitosan/montmorillonite microparticles confers changes in Spinacia oleracea L. Sustain 13:9903. https://doi.org/10.3390/su13179903
Haoliang Y, Matthew TH, Ke L, Bin W, Puyu F, Fahad S, Holger M, Rui Y, De LL, Sotirios A, Isaiah H, Xiaohai T, Jianguo M, Yunbo Z, Meixue Z (2022) Crop traits enabling yield gains under more frequent extreme climatic events. Sci Total Environ 808:152170. https://doi.org/10.1016/j.scitotenv.2021.152170
Hasanuzzaman M, Fujita M, Oku H, Nahar K, Hawrylak-Nowak B (2018a) Plant Nutr Abiotic Stress Tolerance. https://doi.org/10.1007/978-981-10-9044-8
Hasanuzzaman M, Oku H, Nahar K, Bhuyan MHMB, Mahmud JA, Baluska F, Fujita M (2018b) Nitric oxide-induced salt stress tolerance in plants: ROS metabolism, signaling, and molecular interactions. Plant Biotechnol Report 12(2):77–92. https://doi.org/10.1007/s11816-018-0480-0
He P, Yang L, Xu X, Zhao S, Chen F, Li S, Tu S, Jin J, Johnston AM (2015) Temporal and spatial variation of soil available potassium in China (1990–2012). Field Crop Res 173:49–56. https://doi.org/10.1016/j.fcr.2015.01.003
Holland C, Ryden P, Edwards CH, Grundy MM (2020) Plant cell walls: impact on nutrient bioaccessibility and digestibility. Foods 9(2). https://doi.org/10.3390/foods9020201
Holzmann D, Bethmann S, Jahns P (2022) Zeaxanthin epoxidase activity is downregulated by hydrogen peroxide. Plant Cell Physiol 63(8):1091–1100. https://doi.org/10.1093/pcp/pcac081
Ibad U, Dost M, Maria M, Shadman K, Muhammad A, Fahad S, Muhammad I, Ishaq AM, Aizaz A, Muhammad HS, Muhammad S, Farhana G, Muhammad I, Muhammad ASR, Hafiz MH, Wajid N, Shah S, Jabar ZKK, Masood A, Naushad A, Rasheed Akbar M, Shah MK, Jan B (2022) Comparative effects of biochar and NPK on wheat crops under different management systems. Crop Pasture Sci. https://doi.org/10.1071/CP21146
Ibrar H, Muqarrab A, Adel MG, Khurram S, Omer F, Shahid I, Fahim N, Shakeel A, Viliam B, Marian B, Al Obaid S, Fahad S, Subhan D, Suleyman T, Hanife AKÇA, Rahul D (2021) Improvement in growth and yield attributes of cluster bean through optimization of sowing time and plant spacing under climate change Scenario. Saudi J Bio Sci. https://doi.org/10.1016/j.sjbs.2021.11.018
Ihsan MZ, Abdul K, Manzer HS, Liaqat A, Ritesh K, Hayssam MA, Amar M, Fahad S (2022) The response of triticum aestivum treated with plant growth regulators to acute day/night temperature rise. J Plant Growth Regul. https://doi.org/10.1007/s00344-022-10574-9
Ippolito JA, Cui L, Kammann C, Wrage-Mönnig N, Estavillo JM, Fuertes-Mendizabal T, Cayuela ML, Sigua G, Novak J, Spokas K (2020) Feedstock choice, pyrolysis temperature and type influence biochar characteristics: a comprehensive meta-data analysis review. Biochar 2(4):421–438. https://doi.org/10.1007/s42773-020-00067-x
Iqbal S, Hussain S, Qayyaum MA, Ashraf M (2020) The response of maize physiology under salinity stress and its coping strategies. Plant Stress Physiol 1-25. https://doi.org/10.5772/intechopen.92213
Janpen C, Kanthawang N, Inkham C, Tsan FY, Sommano SR (2019) Physiological responses of hydroponically-grown Japanese mint under nutrient deficiency. PeerJ 7:e7751. https://doi.org/10.7717/peerj.7751
Kätterer T, Roobroeck D, Andrén O, Kimutai G, Karltun E, Kirchmann H, Nyberg G, Vanlauwe B, Röing de Nowina K (2019) Biochar addition persistently increased soil fertility and yields in maize-soybean rotations over 10 years in sub-humid regions of Kenya. Field Crop Res 235:18–26. https://doi.org/10.1016/j.fcr.2019.02.015
Khalid S, Shahid M, Murtaza B, Bibi I, Naeem MA, Niazi NK (2020) A critical review of different factors governing the fate of pesticides in soil under biochar application. Sci Total Environ 711:134645. https://doi.org/10.1016/j.scitotenv.2019.134645
Khan M, Trivellini A, Fatma M, Masood A, Francini A, Iqbal N, Ferrante A, Khan NA (2015) Role of ethylene in responses of plants to nitrogen availability. Front Plant Sci 6:927. https://doi.org/10.3389/fpls.2015.00927
Khan Z, Khan MN, Zhang K, Luo T, Zhu K, Hu L (2021) The application of biochar alleviated the adverse effects of drought on the growth, physiology, yield and quality of rapeseed through regulation of soil status and nutrients availability. Ind Crop Prod 171:113878. https://doi.org/10.1016/j.indcrop.2021.113878
Khatun M, Sarkar S, Era FM, Islam AKMM, Anwar MP, Fahad S, Datta R, Islam AKMA (2021) Drought stress in grain legumes: effects, tolerance mechanisms and management. Agron 11:2374. https://doi.org/10.3390/agronomy11122374
Kim JS, Jeon BW, Kim J (2021) Signaling peptides regulating abiotic stress responses in plants. Front Plant Sci 12. https://doi.org/10.3389/fpls.2021.704490
Kong M, Kang J, Han C-L, Gu Y-J, Siddique KH, Li F-MJA (2020) Nitrogen, phosphorus, and potassium resorption responses of Alfalfa to increasing soil water and P availability in a semi-arid environment. Agronomy 10(2):310. https://doi.org/10.3390/agronomy10020310
Laranjeira S, Fernandes-Silva A, Reis S, Torcato C, Raimundo F, Ferreira L, Carnide V, Marques G (2021) Inoculation of plant growth promoting bacteria and arbuscular mycorrhizal fungi improve chickpea performance under water deficit conditions. Appl Soil Ecol 164:103927. https://doi.org/10.1016/j.apsoil.2021.103927
Lehmann J (2007) A handful of carbon. Nature 447: 143–144. https://doi.org/10.1038/447143a
Lehmann J, Joseph S (2015) Biochar for environmental management, 2nd edn. Science, Technology and Implementation, p 944. ISBN-13: 978-0415704151. https://doi.org/10.4324/9780203762264
Lehmann J, Rillig MC, Thies J, Masiello CA, Hockaday WC, Crowley D (2011) Biochar effects on soil biota—a review. Soil Biol Biochem 43:1812–1836. https://doi.org/10.1016/j.soilbio.2011.04.022
Leng L, Huang H, Li H, Li J, Zhou W (2019) Biochar stability assessment methods: a review. Sci Total Environ 647:210–222. https://doi.org/10.1016/j.scitotenv.2018.07.402
Li H, Li Y, Xu Y, Lu X (2020a) Biochar phosphorus fertilizer effects on soil phosphorus availability. Chemosphere 244:125471. https://doi.org/10.1016/j.chemosphere.2019.125471
Li J, Liu LN, Meng Q, Fan H, Sui N (2020b) The roles of chloroplast membrane lipids in abiotic stress responses. Plant Signal Behav 15(11):1807152. https://doi.org/10.1080/15592324.2020.1807152
Liu S, Tang W, Yang F, Meng J, Chen W, Li X (2017) Influence of biochar application on potassium-solubilizing Bacillus mucilaginosus as potential biofertilizer. Prep Biochem Biotechnol 47(1):32–37. https://doi.org/10.1080/10826068.2016.1155062
Manoj KM, Gideon DA, Parashar A, Haarith D, Manekkathodi A (2020) Role of thylakoid membranes in oxygenic photosynthesis: a comparative perspective using murburn concept. https://doi.org/10.1080/07391102.2021.1953607
Mehmood K, Bao Y, Saifullah BS, Dahlawi S, Yaseen M, Abrar MM, Srivastava P, Fahad S, Faraj TK (2022) Contributions of open biomass burning and crop straw burning to air quality: current research paradigm and future outlooks. Front Environ Sci 10:852492. https://doi.org/10.3389/fenvs.2022.852492
Michaud M, Jouhet J (2019) Lipid trafficking at membrane contact sites during plant development and stress response. Front Plant Sci 10:2. https://doi.org/10.3389/fpls.2019.00002
Minhas WA, Hussain M, Mehboob N, Nawaz A, UL-Allah S, Rizwan MS, Hassan Z (2020) Synergetic use of biochar and synthetic nitrogen and phosphorus fertilizers to improves maize productivity and nutrient retention in loamy soil. J Plant Nutr 43(9):1356–1368. https://doi.org/10.1080/01904167.2020.1729804
Mittler R, Zandalinas SI, Fichman Y, Van Breusegem F (2022) Reactive oxygen species signalling in plant stress responses. Nat Rev Mol Cell Biol 23(10):663–679. https://doi.org/10.1038/s41580-022-00499-2
Moriwaki T, Falcioni R, Tanaka FAO, Cardoso KAK, Souza L, Benedito E, Nanni MR, Bonato CM, Antunes WC (2019) Nitrogen-improved photosynthesis quantum yield is driven by increased thylakoid density, enhancing green light absorption. Plant Sci 278:1–11. https://doi.org/10.1016/j.plantsci.2018.10.012
Muhammad I, Khadim D, Fahad S, Imran M, Saud A, Manzer HS, Shah S, ZKK J, Shamsher A, Shah H, Taufiq N, Hafiz MH, Jan B, Wajid N (2022) Exploring the potential effect of Achnatherum splendens L.–derived biochar treated with phosphoric acid on bioavailability of cadmium and wheat growth in contaminated soil. Environ Sci Pollut Res. https://doi.org/10.1007/s11356-021-17950-0
Mwando E, Angessa TT, Han Y, Li C (2020) Salinity tolerance in barley during germination—homologs and potential genes. J Zhejiang Univ Sci B 21(2):93–121. https://doi.org/10.1631/jzus.B1900400
Nadeem F, Farooq M (2019) Application of micronutrients in rice-wheat cropping system of South Asia. Ric Sci 26(6):356–371. https://doi.org/10.1016/j.rsci.2019.02.002
Nguyen TTN, Xu C-Y, Tahmasbian I, Che R, Xu Z, Zhou X, Wallace HM, Bai SH (2017) Effects of biochar on soil available inorganic nitrogen: a review and meta-analysis. Geoderma 288:79–96. https://doi.org/10.1016/j.geoderma.2016.11.004
Niaz A, Abdullah E, Subhan D, Muhammad A, Fahad S, Khadim D, Suleyman T, Hanife A, Anis AS, Mohammad JA, Emre B, ¨Omer SU, Rahul D, Bernard RG (2022) Mitigation of lead (Pb) toxicity in rice cultivated with either ground water or wastewater by application of acidified carbon. J Environ Manage 307:114521. https://doi.org/10.1016/j.jenvman.2022.114521
Nieves-Cordones M, López-Delacalle M, Ródenas R, Martínez V, Rubio F, Rivero RM (2019) Critical responses to nutrient deprivation: A comprehensive review on the role of ROS and RNS. Environ Exp Bot 161:74–85. https://doi.org/10.1016/j.envexpbot.2018.10.039
Ogden M, Hoefgen R, Roessner U, Persson S, Khan GA (2018) Feeding the Walls: how does nutrient availability regulate cell wall composition? Int J Mol Sci 19(9):2691. https://doi.org/10.3390/ijms19092691
Oram NJ, van de Voorde TF, Ouwehand G-J, Bezemer TM, Mommer L, Jeffery S, Van Groenigen JW (2014) Soil amendment with biochar increases the competitive ability of legumes via increased potassium availability. Agr Ecosyst Environ 191:92–98. https://doi.org/10.1016/j.agee.2014.03.031
Oustric J, Herbette S, Quilichini Y, Morillon R, Giannettini J, Berti L, Santini J (2021) Tetraploid Citrumelo 4475 rootstocks improve diploid common clementine tolerance to long-term nutrient deficiency. Sci Rep 11(1):1–15. https://doi.org/10.1038/s41598-021-88383-5
Pandey N (2018) Role of plant nutrients in plant growth and physiology. In: Plant nutrients and abiotic stress tolerance. Springer, pp 51–93. https://doi.org/10.1007/978-981-10-9044-8_2
Papageorgiou A, Azzi ES, Enell A, Sundberg C (2021) Biochar produced from wood waste for soil remediation in Sweden: carbon sequestration and other environmental impacts. Sci Total Environ 776:145953. https://doi.org/10.1016/j.scitotenv.2021.145953
Park MH, Jeong S, Kim JY (2019) Adsorption of NH3-N onto rice straw-derived biochar. J Environ Chem Eng 7(2):103039. https://doi.org/10.1016/j.jece.2019.103039
Pathak J, Ahmed H, Kumari N, Pandey A, Sinha RP (2020) Role of calcium and potassium in amelioration of environmental stress in plants. In: Protective chemical agents in the amelioration of plant abiotic stress: biochemical and molecular perspectives. Wiley, pp 535–562. https://doi.org/10.1002/9781119552154.ch27
Peng YY, Liao LL, Liu S, Nie MM, Li J, Zhang LD, Ma JF, Chen ZC (2019a) Magnesium deficiency triggers SGR–mediated chlorophyll degradation for magnesium remobilization. Plant Physiol 181(1):262–275. https://doi.org/10.1104/pp.19.00610
Peng Z, Feng L, Wang X, Miao X (2019b) Adaptation of Synechococcus sp. PCC 7942 to phosphate starvation by glycolipid accumulation and membrane lipid remodeling. Biochim Biophys Acta Mol Cell Biol Lipids BBA-Mol Cell Biol Lipid 1864(12):158522. https://doi.org/10.1016/j.bbalip.2019.158522
Phillips CL, Light SE, Gollany HT, Chiu S, Wanzek T, Meyer K, Trippe KM (2020) Can biochar conserve water in Oregon agricultural soils? Soil Tillage Res 198:104525. https://doi.org/10.1016/j.still.2019.104525
Pickering G, Mazur A, Trousselard M, Bienkowski P, Yaltsewa N, Amessou M, Noah L, Pouteau E (2020) Magnesium status and stress: the vicious circle concept revisited. Nutrients 12(12):3672. https://doi.org/10.3390/nu12123672
Posso DA, Borella J, Reissig GN, do Amarante L, Bacarin MA (2020) Nitrate-mediated maintenance of photosynthetic process by modulating hypoxic metabolism of common bean plants. Acta Physiologiae Plantarum 42(7):1–17. https://doi.org/10.1007/s11738-020-03107-y
Praveen A, Gupta M (2018) Nitric oxide confronts arsenic stimulated oxidative stress and root architecture through distinct gene expression of auxin transporters, nutrient related genes and modulates biochemical responses in Oryza sativa L. Environ Pollut 240:950–962. https://doi.org/10.1016/j.envpol.2018.04.096
Prescott CE, Grayston SJ, Helmisaari H-S, Kaštovská E, Körner C, Lambers H, Meier IC, Millard P, Ostonen I (2020) Surplus carbon drives allocation and plant–soil interactions. Trends Ecol Evol 35(12):1110–1118. https://doi.org/10.1016/j.tree.2020.08.007
Purbajanti ED, Slamet W, Fuskhah E (2019) Effects of organic and inorganic fertilizers on growth, activity of nitrate reductase and chlorophyll contents of peanuts (Arachis hypogaea L.), IOP conference series: earth and environmental science. IOP Publishing. https://doi.org/10.1088/1755-1315/250/1/012048
Qin ZH, Rahman NU, Ahmad A, Wang Y-p, Sakhawat S, Ehmet N, Shao W-j, Muhammad I, Kun S, Rui L, Fazal S, Fahad S (2022) Range expansion decreases the reproductive fitness of Gentiana officinalis (Gentianaceae). Sci Rep 12:2461. https://doi.org/10.1038/s41598-022-06406-1
Rahimzadeh N, Khormali F, Olamaee M, Amini A, Dordipour E (2015) Effect of canola rhizosphere and silicate dissolving bacteria on the weathering and K release from indigenous glauconite shale. Biol Fertil Soils 51(8):973–981. https://doi.org/10.1007/s00374-015-1043-y
Rai KK (2022) Revisiting the critical role of ROS and RNS in plant defense. J Plant Growth Regul:1–26. https://doi.org/10.1007/s00344-022-10804-0
Rajesh KS, Fahad S, Pawan K, Prince C, Talha J, Dinesh J, Prabha S, Debanjana S, Prathibha MD, Bandana B, Akash H, Gupta NK, Rekha S, Devanshu D, Dalpat LS, Ke L, Matthew TH, Saud S, Adnan NS, Taufiq N (2022) Beneficial elements: new players in improving nutrient use efficiency and abiotic stress tolerance. Plant Growth Regul. https://doi.org/10.1007/s10725-022-00843-8
Rehana S, Asma Z, Shakil A, Anis AS, Rana KI, Shabir H, Subhan D, Umber G, Fahad S, Jiri K, Al Obaid S, Mohammad JA, Rahul D (2021) Proteomic changes in various plant tissues associated with chromium stress in sunflower. Saudi J Bio Sci. https://doi.org/10.1016/j.sjbs.2021.12.042
Rodés-Guirao MRaL (2013) Future population growth. Published online at OurWorldInData.org. Retrieved from: https://ourworldindata.org/future-population-growth [Online Resource]
Saffari N, Hajabbasi M, Shirani H, Mosaddeghi M, Mamedov A (2020) Biochar type and pyrolysis temperature effects on soil quality indicators and structural stability. J Environ Manage 261:110190. https://doi.org/10.1016/j.jenvman.2020.110190
Saghaiesh SP, Souri MK (2018) Root growth characteristics of Khatouni melon seedlings as affected by potassium nutrition. Acta Sci Pol Hortorum Cultus 17(5):191–198. https://doi.org/10.24326/asphc.2018.5.17
Sajjad H, Muhammad M, Ashfaq A, Fahad S, Wajid N, Hafiz MH, Ghulam MS, Behzad M, Muhammad T, Saima P (2021a) Using space–time scan statistic for studying the effects of COVID-19 in Punjab, Pakistan: a guideline for policy measures in regional Agriculture. Environ Sci Pollut Res. https://doi.org/10.1007/s11356-021-17433-2
Sajjad H, Muhammad M, Ashfaq A, Nasir M, Hafiz MH, Muhammad A, Muhammad I, Muhammad U, Hafiz UF, Fahad S, Wajid N, Hafiz MRJ, Mazhar A, Saeed AQ, Amjad F, Muhammad SK, Mirza W (2021b) Satellite-based evaluation of temporal change in cultivated land in Southern Punjab (Multan region) through dynamics of vegetation and land surface temperature. Open Geo Sci 13:1561–1577. https://doi.org/10.1515/geo-2020-0298
Sales AC, Campos CNS, de Souza Junior JP, da Silva DL, Oliveira KS, de Mello PR, Teodoro LPR, Teodoro PE (2021) Silicon mitigates nutritional stress in quinoa (Chenopodium quinoa Willd.). Sci Rep 11(1):1–16. https://doi.org/10.1038/s41598-021-94287-1
Sana U, Shahid A, Yasir A, Farman UD, Syed IA, Mirza MFAB, Fahad S, Al-Misned F, Usman A, Xinle G, Ghulam N, Kunyuan W (2022) Bifenthrin induced toxicity in Ctenopharyngodon idella at an acute concentration: A multi-biomarkers based study. J King Saud Uni–Sci 34(2022):101752. https://doi.org/10.1016/j.jksus.2021.101752
Sattar A, Sher A, Ijaz M, Ul-Allah S, Butt M, Irfan M, Rizwan MS, Ali H, Cheema MA (2020) Interactive effect of biochar and silicon on improving morpho-physiological and biochemical attributes of maize by reducing drought hazards. J Soil Sci Plant Nutr 20(4):1819–1826. https://doi.org/10.1007/s42729-020-00253-7
Saud S, Chen Y, Long B, Fahad S, Sadiq A (2013) The different impact on the growth of cool season turf grass under the various conditions on salinity and drought stress. Int J Agric Sci Res 3:77–84
Saud S, Li X, Chen Y, Zhang L, Fahad S, Hussain S, Sadiq A, Chen Y (2014) Silicon application increases drought tolerance of Kentucky bluegrass by improving plant water relations and morph physiological functions. Sci World J 2014:1–10. https://doi.org/10.1155/2014/368694
Saud S, Chen Y, Fahad S, Hussain S, Na L, Xin L, Alhussien SA (2016) Silicate application increases the photosynthesis and its associated metabolic activities in Kentucky bluegrass under drought stress and post-drought recovery. Environ Sci Pollut Res 23(17):17647–17655. https://doi.org/10.1007/s11356-016-6957-x
Saud S, Fahad S, Yajun C, Ihsan MZ, Hammad HM, Nasim W, Amanullah J, Arif M, Alharby H (2017) Effects of nitrogen supply on water stress and recovery mechanisms in kentucky bluegrass plants. Front Plant Sci 8:983. https://doi.org/10.3389/fpls.2017.00983
Saud S, Fahad S, Cui G, Chen Y, Anwar S (2020) Determining nitrogen isotopes discrimination under drought stress on enzymatic activities, nitrogen isotope abundance and water contents of Kentucky bluegrass. Sci Rep 10:6415. https://doi.org/10.1038/s41598-020-63548-w
Saud S, Fahad S, Hassan S (2022a) Developments in the investigation of nitrogen and oxygen stable isotopes in atmospheric nitrate. Sustain Chem Climate Action 1:100003. https://doi.org/10.1016/j.scca.2022.100003
Saud S, Li X, Jiang Z, Fahad S, Hassan S (2022b) Exploration of the phytohormone regulation of energy storage compound accumulation in microalgae. Food Energy Secur 10:e418. https://doi.org/10.1002/fes3.418
Shah S, Shah H, Liangbing X, Xiaoyang S, Shahla A, Fahad S (2022) The physiological function and molecular mechanism of hydrogen sulfide resisting abiotic stress in plants. Brazil J Botany. https://doi.org/10.1007/s40415-022-00785-5
Shaheen SM, Antoniadis V, Shahid M, Yang Y, Abdelrahman H, Zhang T, Hassan NE, Bibi I, Niazi NK, Younis SA (2022) Sustainable applications of rice feedstock in agro-environmental and construction sectors: a global perspective. Renew Sustain Energy Rev 153:111791. https://doi.org/10.1016/j.rser.2021.111791
Souri MK, Hatamian M (2019) Aminochelates in plant nutrition: a review. J Plant Nutr 42(1):67–78. https://doi.org/10.1080/01904167.2018.1549671
Suliman W, Harsh JB, Abu-Lail NI, Fortuna A-M, Dallmeyer I, Garcia-Pérez M (2017) The role of biochar porosity and surface functionality in augmenting hydrologic properties of a sandy soil. Sci Total Environ 574:139–147. https://doi.org/10.1016/j.scitotenv.2016.09.025
Sung J, Yun H, Back S, Fernie AR, Kim YX, Lee Y, Lee S, Lee D, Kim J (2018) Changes in mineral nutrient concentrations and C-N metabolism in cabbage shoots and roots following macronutrient deficiency. J Plant Nutr Soil Sci 181(5):777–786. https://doi.org/10.1002/jpln.201800001
Tang J, Zhang S, Zhang X, Chen J, He X, Zhang Q (2020) Effects of pyrolysis temperature on soil-plant-microbe responses to Solidago canadensis L.-derived biochar in coastal saline-alkali soil. Sci Total Environ 731:138938. https://doi.org/10.1016/j.scitotenv.2020.138938
Thor K (2019) Calcium—nutrient and messenger. Front Plant Sci 10:440. https://doi.org/10.3389/fpls.2019.00440
Tian X-Y, He D-D, Bai S, Zeng W-Z, Wang Z, Wang M, Wu L-Q, Chen Z-C (2021) Physiological and molecular advances in magnesium nutrition of plants. Plant and Soil 468(1):1–17. https://doi.org/10.1007/s11104-021-05139-w
Torabian S, Farhangi-Abriz S, Rathjen J (2018) Biochar and lignite affect H+-ATPase and H+-PPase activities in root tonoplast and nutrient contents of mung bean under salt stress. Plant Physiol Biochem 129:141–149. https://doi.org/10.1016/j.plaphy.2018.05.030
Trazzi P, Leahy JJ, Hayes MH, Kwapinski W (2016) Adsorption and desorption of phosphate on biochars. J Environ Chem Eng 4(1):37–46. https://doi.org/10.1016/j.jece.2015.11.005
Uchimiya M, Hiradate S, Antal MJ Jr (2015) Dissolved phosphorus speciation of flash carbonization, slow pyrolysis, and fast pyrolysis biochars. ACS Sustain Chem Eng 3(7):1642–1649. https://doi.org/10.1021/acssuschemeng.5b00336
van der Bom FJ, Williams A, Bell MJ (2020) Root architecture for improved resource capture: trade-offs in complex environments. J Exp Bot 71(19):5752–5763. https://doi.org/10.1093/jxb/eraa324
Veronese N, Demurtas J, Pesolillo G, Celotto S, Barnini T, Calusi G, Caruso MG, Notarnicola M, Reddavide R, Stubbs B (2020) Magnesium and health outcomes: an umbrella review of systematic reviews and meta-analyses of observational and intervention studies. Eur J Nutr 59(1):263–272. https://doi.org/10.1007/s00394-019-01905-w
Wacal C, Ogata N, Basalirwa D, Handa T, Sasagawa D, Acidri R, Ishigaki T, Kato M, Masunaga T, Yamamoto S (2019) Growth, seed yield, mineral nutrients and soil properties of sesame (Sesamum indicum L.) as influenced by biochar addition on upland field converted from paddy. Agronomy 9(2):55. https://doi.org/10.3390/agronomy9020055
Wang T, Chen Y, Tabuchi A, Cosgrove DJ, Hong M (2016) The target of β-expansin EXPB1 in maize cell walls from binding and solid-state NMR studies. Plant Physiol 172(4):2107–2119. https://doi.org/10.1104/pp.16.01311
Wiqar A, Arbaz K, Muhammad Z, Ijaz A, Muhammad A, Fahad S (2022) Relative efficiency of biochar particles of different sizes for immobilising heavy metals and improving soil properties. Crop Pasture Sci. https://doi.org/10.1071/CP20453
Wu H, Shabala L, Shabala S, Giraldo JP (2018) Hydroxyl radical scavenging by cerium oxide nanoparticles improves Arabidopsis salinity tolerance by enhancing leaf mesophyll potassium retention. Environ Sci Nano 5(7):1567–1583. https://doi.org/10.1039/C8EN00323H
Wu L, Zhang S, Ma R, Chen M, Wei W, Ding X (2021) Carbon sequestration under different organic amendments in saline-alkaline soils. Catena 196:104882. https://doi.org/10.1016/j.catena.2020.104882
Xie K, Cakmak I, Wang S, Zhang F, Guo S (2021) Synergistic and antagonistic interactions between potassium and magnesium in higher plants. The Crop Journal 9(2):249–256. https://doi.org/10.1016/j.cj.2020.10.005
Xu D, Cao J, Li Y, Howard A, Yu K (2019) Effect of pyrolysis temperature on characteristics of biochars derived from different feedstocks: A case study on ammonium adsorption capacity. Waste Manag 87:652–660. https://doi.org/10.1016/j.wasman.2019.02.049
Xue B, Huang L, Li X, Lu J, Gao R, Kamran M, Fahad S (2022) Effect of clay mineralogy and soil organic carbon in aggregates under straw incorporation. Agron 12:534. https://doi.org/10.3390/agronomy12020534
Yang A, Akhtar SS, Li L, Fu Q, Li Q, Naeem MA, He X, Zhang Z, Jacobsen S-E (2020) Biochar mitigates combined effects of drought and salinity stress in Quinoa. Agronomy 10(6):912. https://doi.org/10.3390/agronomy10060912
Yang R, Dai P, Wang B, Jin T, Liu K, Fahad S, Harrison MT, Man J, Shang J, Meinke H, Deli L, Xiaoyan W, Yunbo Z, Meixue Z, Yingbing T, Haoliang Y (2022) Over-optimistic projected future wheat yield potential in the north china plain: the role of future climate extremes. Agron 12:145. https://doi.org/10.3390/agronomy12010145
Yoo Y, Park J-C, Cho M-H, Yang J, Kim C-Y, Jung K-H, Jeon J-S, An G, Lee S-W (2018) Lack of a cytoplasmic RLK, required for ROS homeostasis, induces strong resistance to bacterial leaf blight in rice. Front Plant Sci 9:577. https://doi.org/10.3389/fpls.2018.00577
Zaman I, Ali M, Shahzad K, Tahir MS, Matloob A, Ahmad W, Alamri S, Khurshid MR, Qureshi MM, Wasaya A, Khurram SB, Manzer HS, Fahad S, Rahul D (2021) Effect of plant spacings on growth, physiology, yield and fiber quality attributes of cotton genotypes under nitrogen fertilization. Agron 11:2589. https://doi.org/10.3390/agronomy11122589
Zhang H, Li Y, Zhu J-K (2018a) Developing naturally stress-resistant crops for a sustainable agriculture. Nat Plant 4(12):989–996. https://doi.org/10.1038/s41477-018-0309-4
Zhang X, Wu H, Chen L, Liu L, Wan X (2018b) Maintenance of mesophyll potassium and regulation of plasma membrane H+-ATPase are associated with physiological responses of tea plants to drought and subsequent rehydration. The Crop Journal 6(6):611–620. https://doi.org/10.1016/j.cj.2018.06.001
Zhang L, Wang N, Yang M, Ding K, Wang Y-Z, Huo D, Hou C (2019) Lipid accumulation and biodiesel quality of Chlorella pyrenoidosa under oxidative stress induced by nutrient regimes. Renew Energy 143:1782–1790. https://doi.org/10.1016/j.renene.2019.05.081
Zhang Z, Wu P, Zhang W, Yang Z, Liu H, Ahammed GJ, Cui J (2020) Calcium is involved in exogenous NO-induced enhancement of photosynthesis in cucumber (Cucumis sativus L.) seedlings under low temperature. Sci Hortic 261:108953. https://doi.org/10.1016/j.scienta.2019.108953
Zhao L, Cao X, Zheng W, Scott JW, Sharma BK, Chen X (2016) Copyrolysis of biomass with phosphate fertilizers to improve biochar carbon retention, slow nutrient release, and stabilize heavy metals in soil. ACS Sustain Chem Eng 4(3):1630–1636. https://doi.org/10.1021/acssuschemeng.5b01570
Zhao W, Zhou Q, Tian Z, Cui Y, Liang Y, Wang H (2020) Apply biochar to ameliorate soda saline-alkali land, improve soil function and increase corn nutrient availability in the Songnen Plain. Sci Total Environ 722:137428. https://doi.org/10.1016/j.scitotenv.2020.137428
Zhou L, Xu D, Li Y, Pan Q, Wang J, Xue L, Howard A (2019) Phosphorus and nitrogen adsorption capacities of biochars derived from feedstocks at different pyrolysis temperatures. Water 11(8):1559. https://doi.org/10.3390/w11081559
Zhou Y, Tang Y, Hu C, Zhan T, Zhang S, Cai M, Zhao X (2021) Soil applied Ca, Mg and B altered phyllosphere and rhizosphere bacterial microbiome and reduced Huanglongbing incidence in Gannan Navel Orange. Sci Total Environ 791:148046. https://doi.org/10.1016/j.scitotenv.2021.148046
Zhu X, Chen B, Zhu L, Xing B (2017) Effects and mechanisms of biochar-microbe interactions in soil improvement and pollution remediation: a review. Environ Pollut 227:98–115. https://doi.org/10.1016/j.envpol.2017.04.032
Zhu S, Zhao J, Zhao N, Yang X, Chen C, Shang J (2020) Goethite modified biochar as a multifunctional amendment for cationic Cd (II), anionic As (III), roxarsone, and phosphorus in soil and water. J Clean Prod 247:119579. https://doi.org/10.1016/j.jclepro.2019.119579
Zirek NS, Ozlem U (2020) The developmental and metabolic effects of different magnesium dozes in pepper plants under salt stress. Notulae Botanicae Horti Agrobotanici Cluj-Napoca 48(2):967–977. https://doi.org/10.15835/nbha48211943
Author information
Authors and Affiliations
Corresponding author
Editor information
Editors and Affiliations
Rights and permissions
Copyright information
© 2023 The Author(s), under exclusive license to Springer Nature Switzerland AG
About this chapter
Cite this chapter
Javeed, H.M.R. et al. (2023). Biochar Application to Soil for Mitigation of Nutrients Stress in Plants. In: Fahad, S., Danish, S., Datta, R., Saud, S., Lichtfouse, E. (eds) Sustainable Agriculture Reviews 61. Sustainable Agriculture Reviews, vol 61. Springer, Cham. https://doi.org/10.1007/978-3-031-26983-7_8
Download citation
DOI: https://doi.org/10.1007/978-3-031-26983-7_8
Published:
Publisher Name: Springer, Cham
Print ISBN: 978-3-031-26982-0
Online ISBN: 978-3-031-26983-7
eBook Packages: Biomedical and Life SciencesBiomedical and Life Sciences (R0)