REVIEW article

Front. Plant Sci., 13 January 2025

Sec. Plant Nutrition

Volume 15 - 2024 | https://doi.org/10.3389/fpls.2024.1479925

Unlocking biochar impacts on abiotic stress dynamics: a systematic review of soil quality and crop improvement

  • 1. Horticultural and Herbal Crop Environment Division, Soil Management Laboratory, National Institute of Horticultural and Herbal Science, Rural Development Administration, Wanju-gun, Republic of Korea

  • 2. Division of Plant Molecular Biology and Biotechnology, Department of Biosciences, Rajagiri College of Social Sciences, Kochi, Kerala, India

  • 3. Microbial Safety Division, National Institute of Agricultural Sciences, Rural Development Administration, Wanju-gun, Republic of Korea

  • 4. Institute for Fiber Engineering and Science (IFES), Interdisciplinary Cluster for Cutting Edge Research (ICCER), National University Corporation Shinshu University, Ueda, Japan

  • 5. Department of Biomaterials, Saveetha Dental College and Hospitals, Saveetha Institute of Medical and Technical Sciences (SIMATS), Saveetha University, Chennai, India

Abstract

Global agricultural challenges, especially soil degradation caused by abiotic stresses, significantly reduce crop productivity and require innovative solutions. Biochar (BC), a biodegradable product derived from agricultural and forestry residues, has been proven to significantly enhance soil quality. Although its benefits for improving soil properties are well-documented, the potential of BC to mitigate various abiotic stresses-such as drought, salinity, and heavy metal toxicity-and its effect on plant traits need further exploration. This review aims to elucidate BC production by highlighting primary feedstock’s and synthesis techniques, and examining its role in boosting soil decomposition efficiency and fertility, which are pivotal for sustainable crop growth. This review also discuss how BC can enhance the nutritional and chemical properties of soil under different abiotic stress conditions, emphasizing its capacity to foster crop growth and development in adverse environments. Furthermore, this article serves as a comprehensive resource for agricultural researchers in understanding the importance of BC in promoting sustainable agriculture, and addressing environmental challenges. Ultimately, this review highlights critical knowledge gaps and proposes future research avenues on the bio-protective properties of BC against various abiotic stresses, paving the way for the commercialization of BC applications on a large scale with cutting-edge technologies.

Highlights

  • BC ameliorates physico-chemical properties of soil against environmental stress.

  • It serves as a significant nutritional reservoir for plant growth improvement.

  • BC acts as a key player in mitigating abiotic stress tolerance for sustainable agriculture.

  • Further studies are needed on expression pattern and characterization of genes in BC’s protective roles against abiotic stress.

  • Emphasis should be placed on innovative uses of BC for agricultural stress management.

1 Introduction

Soil degradation, severe soil contamination and loss of soil fertility provoke a global threat to food security and agricultural sustainability. Rising food deficits and climate change need a green solution for improving soil quality and diminishing ecological agriculture impacts to ameliorate crop productivity. The excessive use of chemical fertilizers with salt and other acidic components reduces the productivity of crops by triggering soil quality via soil deterioration, soil acidity, and poor soil aggregate structures (Wu et al., 2023). Quality of soil is commonly affected by soil organic matter (OM), electrical conductivity (EC), and soil depth, which cause salinization, compaction, nutrient deficiency, erosion, loss of biodiversity and desertification, which all lead to soil fertility reduction (; Lal, 2015). In addition, soil nutrient depletion was directly associated with food insecurity due to unsustainable land use. To combat this, various soil additives are implemented to augment soil nutrients, including composts, inorganic chemical fertilizers, seaweed, organic manures, mulches, clay minerals, nanomaterials and sewage sludge, etc (; Yasmeen et al., 2022). Since most of these management approaches have less or no impact on the storage of soil carbon (C), prompt organic C (OC) decomposition results in the emission of carbon-di-oxide (CO2), thereby reducing the efficiency of C balance (; ). Hence, sustainable and reliable resource management techniques are urgently needed to mitigate global soil contamination and restore soil quality (Pradhan et al., 2018).

Global agricultural productivity has been significantly impacted by various abiotic stressors, which are major limiting factors affecting soil quality. Abiotic stressors such as drought, soil salinity, and heavy metal accumulation contribute to over 50% of crop production losses and affect 91% of the world’s cropland (Younis et al., 2020). Among these, heavy metal pollution, a notable consequence of anthropogenic activities, has significantly increased since the industrial revolution. For instance, high concentrations of heavy metals in soils adversely affect plant physiology, metabolism, and biochemical processes, leading to reduced growth, biomass, and yield of plants (Goyal et al., 2020). In addition to heavy metal pollution, reduced precipitation due to climate change has exacerbated global drought conditions. Drought stress reduces cell turgor and negatively impacts plant growth. It reduces shoot growth, limiting the production and transfer of photosynthetic materials, which ultimately decreases plant growth and yield (Nour et al., 2024). For example, severe drought stress reduced yield of rice (Oryza sativa) (53-92%), wheat (Triticum aestivum) (57%), maize (Zea mays) (63-87%), soybean (Glycine max) (46-71%) and chickpea (Cicer arietinum) (45-69%) (). Similarly, salinity stress reduces crop yield, with declines ranging from 5-50% due to osmotic stress, ionic toxicity, and nutrient imbalances (Okorogbona et al., 2015).

To meet the projected increase in food demand for an estimated global population of 9 to 10 billion people by 2050 (Van Dijk et al., 2021), various strategies have been implemented to improve crop performance under abiotic stress. These strategies include breeding techniques, agronomic practices, seed priming, microbial seed treatment, microorganism inoculation, grafting, and the use of plant growth regulators and osmoprotectants (Gupta and Shrestha, 2023; Oyebamiji et al., 2024). Especially, farmers use pesticides and hazardous chemical fertilizers to cultivate maximum crops in a minimal area, which further lowers land quality and causes soil degradation, contamination, erosion and water pollution (; Oliver and Gregory, 2015; Pradhan et al., 2018). To combat this, the application of biochar (BC) has recently emerged as a cost-effective and environment friendly strategy to enhance crop tolerance to abiotic stress.

BC is a highly stable carbonaceous residue resulting from the thermochemical degradation of various feedstocks, such as crop residues, mill residues, agricultural wastes, food wastes, animal manure, and forestry wastes (Tomczyk et al., 2020). BC is valued for its micro-pores and high cation exchange capacity (CEC), which do not exacerbate environmental conditions. It is primarily composed of oxygen (O2), nitrogen (N), hydrogen (H), C, and aromatic and alkyl matter (Nath et al., 2022). BC’s unique structural and functional properties make it a valuable soil amendment for enhancing soil fertility. In USA and China alone, approximately 1.4 BT of agro-biomass waste are generated annually, producing around 420 MT of BC per year (Godlewska et al., 2017; Nath et al., 2022; Kumar et al., 2023). BC has been shown to enhance crop growth and yield under abiotic stresses and in metal-polluted soils. Incorporating BC into infertile or nutrient-deficient soils can improve crop performance, benefit farmers, reduce the use of inorganic fertilizers, and support environmental conservation (; Wani et al., 2022). Raw BC has a limited ability to absorb contaminants from highly polluted water (Jagadeesh and Sundaram, 2023). Furthermore, the small particle size of powdered BC makes it difficult to separate pollutants from the contaminated water (Sivaranjanee et al., 2024). Nowadays, several studies focus on synthesizing novel BCs using nanocomposites to remove aqueous contaminants in an effort to overcome these unfavorable factors (Li et al., 2023; ). This type of nanocomposite-based BC method helps to improve the physical and chemical properties of BC. For instance, the nanocomposite BC exhibits higher porosity, more surface active sites, increased stability, a larger specific surface area, and a wider range of applications compared to the unaltered BC (Pan et al., 2021). Various review articles have well described the synthesis of BC nanocomposites (; ; Lalhriatpuia and Tiwari, 2023). Hence, we can use this type of BC to remove heavy metal pollutants from wastewater and support efforts to improve the aquatic environment. To date, there is no much comprehensive review on the role of BC in alleviating abiotic stresses in plants. This review aims to highlight the production of BC from crop residual biomass and its wide range of applications under abiotic stress conditions. In addition, it provides updated information on BC for improving soil fertility and crop growth. Furthermore, we have discussed what studies should be carried out to understand the exact role of BC in crop development against abiotic stresses. Overall, we believe this review enhances the understanding of the role of crop residue-derived BC in controlling hazardous chemical-based soil amendments, reducing anthropogenic gas emissions, and ensuring environmental sustainability. Apart from this, this review will raise awareness in plant molecular biology researchers to initiate in depth molecular experiments to study about gene regulations on using BC for plant growth.

2 Methodology

Published research articles related to the topic were collected from five scientific databases, including Web of Science, “Scopus,” “PubMed,” “Science Direct,” and “Google Scholar”. The following combinations of search terms were used to collect articles: “role of BC on improving soil properties,” “biochar role in physical and chemical properties of soil,” “BC synthesis methods,” “Effects of biochar on drought stress tolerance in plants,” “Effects of biochar on salinity stress tolerance in plants,” “Effects of biochar on heavy metal stress tolerance in plants,” and “Role of biochar for improving abiotic stress tolerance in plants.” This review included articles published in English up until August 2024. Article titles and abstracts were manually assessed to exclude reports that were not relevant to this review. This review includes only biochar-related topics that enhance abiotic stress tolerance. We excluded only articles published in languages other than English.

3 Feedstock for BC synthesis

Effective selection of feedstock biomass is crucial for optimizing the preparation and yield of BC. Biomass feedstock, a complex solid material, can be categorized as either woody or non-woody. The classification of biomass applied for BC production is mainly based on its source, biological diversity and origin. Plant biomass and organic waste are the two main sources of feedstock used for BC production. In organic waste feedstocks, the use of various types of crop residue biomass for BC production has gained attention due to its economic benefits, environmental advantages, and scientific interest (). Crop residue biomass includes materials that are not classified as processed or field residues, such as leaves, straw, stalks, shells, molasses, roots, husks, peels, bagasse, tree prunes, and pods, sourced from agricultural lands, homes, and industries.

Straws, for instance, can be converted into bioplastics, chemicals, biogases, enzymes, and biocatalysts (). Global estimates indicate that rice straw production is around 800-1000 MT, while wheat straw production is approximately 354 MT, consisting of cellulose (32-47%), lignin (5-24%), and hemicellulose (19-27%) (; Ingrao et al., 2021).

Bagasse, a multicellular lignocellulosic residual fiber extracted from sugarcane and other sources such as pomegranate, pineapple, cashew, and sorghum, is another significant biomass. In 2021, the production of sugarcane reached 1.6 BT, generating 279 MMT of sugarcane bagasse. Bagasse has numerous applications, including biofuel, ceramics, cement additives, bricks, catalysts, concrete, adsorbents, food additives, silage feed, and organic manure ().

Pruned branches from fruit trees like apples, pears, and plums are abundant sources of lignocellulosic biomass. Farmers often incinerate these branches to reduce insect pests and plant diseases, contributing to atmospheric CO2 emissions (Sasaki et al., 2014). In 2010-2011, 1650 tons of pruned pear branches were reported to be discarded and accumulated in fields by the Tokushima Agriculture, Forestry, and Fisheries Technology Support Center of the Fruit Tree Research Institute (Sasaki et al., 2014). Utilizing pruned branches holds potential for BC and biofuel production.

The characteristics of BC derived from diverse crop residues have been compared in numerous studies (Wu et al., 2012; Windeatt et al., 2014; Purakayastha et al., 2015). For instance, Purakayastha et al. (2015) prepared four types of BC from maize stover, pearl millet stalk, rice straw, and wheat straw, finding that maize BC had higher nutrient values, particularly N and phosphorus (P), and greater C stability compared to other crop-derived BC. The study also determined that the total C content was highest in maize BC (66%), followed by pearl millet BC (64%), wheat BC (64%), and rice BC (60%). Another study utilized eight different crop-derived feedstocks, including coconut husk, coconut shell, cotton stalk, olive pomace, palm shell, rice husk, sugarcane bagasse, and wheat straw, for BC production, yielding 28% to 39% of BC. This study also found that high lignin feedstocks produced high-C BC with significant recalcitrance (Windeatt et al., 2014). Wu et al. (2012) demonstrated that rice straw-derived BC had high alkalinity, CEC, and levels of available P and extractable cations, indicating its potential as a fertilizer and soil amendment. Comparative analysis of BC production from various crop residue feedstocks is still limited, and it is necessary to identify the most suitable feedstocks for high-value BC production on a large scale.

While specific data on the annual production of crop residues are unavailable, recent statistics (FAO, 2022; MMR, 2023) indicate that the global cultivation of primary crops increased by 52%, fruits by 55%, and vegetables by 65% between 2000 and 2020 (Figure 1). This significant increase suggests a corresponding rise in crop residue production each year. Converting these residues into BC is a vital sustainable waste management strategy that mitigates climate change, enhances plant growth, and protects the environment.

Figure 1

4 BC synthesis methods

BC can be synthesized through various thermochemical techniques, mainly pyrolysis, gasification, hydrothermal carbonization (HTC), and hydrothermal liquefaction (HTL). The production conditions and physico-chemical properties of used biomass resources for BC synthesis play a vital role in porosity, CEC, specific surface area, functional groups and yield percentage (Nath et al., 2022; Singh et al., 2022). Table 1 presents the different techniques used for BC synthesis.

Table 1

Synthesis techniqueDescriptionAdvantagesReference
Traditional approachFirebrick pits, clay heater, iron and brick retort furnace are used as a reactors and feedstock burnt directly in an open field covered partially with half burned biomass or soil to reduce oxygen supplyLow cost
No energy consumed
Advanced technical skills are not required
Thines et al., 2017; Gabhane et al., 2020; Masek, 2022
Conventional pyrolysisSlowTR: 300-600 °C;
HR: 5-7 °C; min-1
RT: 60-120 min
O2 supply: Nil
Energy consumption was less
Moderate TR
Mendez et al., 2015;
FastTR: >500 °C;
HR: 300 °C; min-1
RT: 0-20 min
O2 supply: Nil
Conversion rate higher
Low RT
Better yield
Higher amount of bio-oil produced
Large-scale BC synthesis
Mendez et al., 2015; Laird et al., 2017
FlashTR: >1000 °C;
HR: 1000 °C; sec-1
RT: 0-1 min
O2 supply: Nil
Fast, effective, and efficient techniqueGabhane et al., 2020;
GasificationTR: >700 °C;
Gasifying agents: Air, steam, O2, and CO2
Humid biomass was used
Produced high quality BC, C2H4, C2H2, other useful fuels and eco-friendly chemicals
Efficacious environmental, and economic benefits
You et al., 2018; ; Zhang et al., 2022
HTCTR: 150-350 °C;
Pressure: 2-10 MPa
RT: Several hours
O2 supply: Less or Nil
Biomass predrying not required
Wet biomass can be directly converted into byproducts
Enhanced hydrophobicity or dewater ability of feedstock
Pauline and Joseph, 2020; ; Moreira et al., 2021
HTLTR: 250-374 °C;
Pressure: 2-25 MPa
No predrying of feedstock required
Recovers <70% as bio-oil and BC
Less water usage
Gollakota et al., 2018;

Details of BC production techniques and advantages.

TR, temperature range; HR, heating rate; RT, residence time; HTC, hydrothermal carbonization; HTL, hydrothermal liquefaction.

4.1 Pyrolysis process

Pyrolysis is an ancient method frequently used for synthesizing BC from biomass in chemical or thermal conversion methods. Pyrolysis is the thermal decomposition of biomass under elevated thermal vibration. During pyrolysis or incineration with a low O2 supply, crop residue breaks down organic components into condensable liquids, noncondensable gases, and char (Jung et al., 2019). Generally, pyrolysis products are composed of flammable methane (CH4), ethane (C2H6), H2, and (carbon monoxide) CO syngas, and liquid products are composed of phenolics, furanics, fatty acids, fine chemicals, biofuels, and solid material of BC (Fahmy et al., 2020; Wang et al., 2020a; ). In accordance with the TR, HR and, RT, conventional pyrolysis can be classified as slow, fast, ultrafast, or flash pyrolysis. In slow pyrolysis, the ranges of HR 5-7 °C; min-1, RT 60-120 min and TR 300-600 °C; can predominantly yield 20-30% syngas, 25-35% bio-oil and 35-45% BC, respectively. Fast pyrolysis occurs without O2 at HR 300 °C; min-1, RT 0-20 min, TR >500 °C; and synthesis 20% of syngas, 60% of bio-oil and 20% of BC. Ultrafast or flash pyrolysis carried out in a fluidized bed reactor with HR ≥1000°C sec-1, RT ≤1 min, TR ≥1000°C yields solid 10-15%, liquid 70-80%, and gas 5-20%. This ultrafast pyrolysis limits wide industrial application since it produces high bio-oil but low levels of BC (Laird et al., 2017; ; ).

The BC yield during the pyrolysis process depends on the type and nature of biomass used. Temperature is the main operating process condition that decides the product efficiency. Generally, the yield of BC decreases and the production of syngas increases when the temperature is increased during the pyrolysis process. For instance, study illustrated that the molecular properties and Cu sorption capacity of BC, derived from Jerusalem artichoke stalks, are closely related to the temperature of pyrolysis (Wei et al., 2019). In that study, the content of O2-containing functional groups in the BC samples decreased, while that of aromatic structures and alkaline mineral components increased, with a rise in pyrolysis temperature (Wei et al., 2019). However, Sawargaonkar et al. (2024) confirmed that peanut shell BC obtained through slow pyrolysis process has greater BC yield as compared to the fast pyrolysis, irrespective of reaction temperature, thus it confirms the effectiveness of the slow pyrolysis mechanism toward the BC production. Wan et al. (2014) compared the characterization of BC derived from rice husk and elm sawdust by fast pyrolysis. They demonstrated that high in ash, while low in volatile and fixed C content found in rice husk derived BC compared to elm sawdust derived BC. This study represents the characteristics of BC was mostly determined by sources of feedstock rather than synthesis process. In general, BC sizes were varied in the range <150 to 2000 µm in pyrolysis process (Liu et al., 2017a; ).

4.2 Gasification

Gasification is an effective waste management process comprising steps like drying, pyrolysis, combustion, and partial oxidation (You et al., 2018; Siwal et al., 2020; ). During gasification, partial oxidation enriches the chemical and textural properties of BC (Yaashikaa et al., 2020). At temperatures ranging from 700-1500°C, the heating rate is rapid, and the reaction duration varies from seconds to minutes, yielding ˜ 85% gas, 10% liquid, and 5% solid (). Depending on availability, air, steam, CO2, O2, and their mixtures used in gasification, significantly enhance BC’s physico-chemical properties, biomass conversion efficiency, product composition, and gas synthesis (You et al., 2018; Maya et al., 2021).

Generally, the BC yield from gasification is lower than that from pyrolysis, this was attributed to C conversion to CO under partial oxidation conditions. Additionally, gasification BC has smaller specific surface areas and total pore volumes compared to slow and fast pyrolysis BC, mainly due to ash melting (pore clogging), pore expansion and collapse, and tar deposition at high combustion and reduction temperatures. However, previous study indicated that higher temperatures and varied gaseous conditions in gasification led to lower BC yields but larger total surface area, higher pH and ash contents, and very low tar content (16-polycyclic aromatic hydrocarbons) (Fryda and Visser, 2015). The particle sizes of gasification BC ranged from under 45 μm to over 2000 μm, showing inconsistency across studies (Griffith et al., 2013; Pujol Pereira et al., 2016; Shen et al., 2016).

4.3 Hydrothermal carbonization

HTC is a highly effective method for converting wet biomass into valuable byproducts without the need for pre-drying. The process operates within a reactor under pressures of 2-10 megapascal (MPa) and temperatures ranging from 150-350 °C;, with minimal or no O2 present, and lasts for several hours. The HTC process involves hydrolysis, dehydration, decarboxylation, aromatization, and re-condensation, producing syngas, hydro-char, and bio-oil (; ).

Similar to pyrolysis, HTC generates a solid product of BC (called hydro-char), which makes up to 50-80%, along with a bio-oil and water mixture (5-20%), and CO2 (2-5%) (Saqib et al., 2019). However, hydro-char produced via HTC typically not classified as BC due to insufficient reaction temperatures, low C content, and an unfavorable O/C and H/C ratio (Wiedner et al., 2013). Recent research shows that combining HTC with pyrolysis can enhance BC quality and stabilize heavy metals in the final solid product (Li et al., 2022a). Olszewski et al. (2019) found that pre-treating brewery spent grains with HTC before pyrolysis significantly improves BC yield and C content, while reducing ash composition. Garlapalli et al. (2016) also observed an increase in C content to 82% in BC produced from the combined HTC and pyrolysis process, compared to 70% from HTC alone. Overall, improving hydro-char is crucial due to its low surface area (<30 m²/g), poor porosity, and the presence of harmful chemicals like furan, furfural, and phenolic compounds, which limit its use in soil improvement applications.

4.4 Hydrothermal liquefaction

In HTL, macro algae and lignocellulosic feedstock are broken down under high pressure and temperature in supercritical or critical water conditions to produce bio-oil, solids, gases, and organic byproducts. This process operates in a water medium at temperatures between 250-374 °C; and pressures of 5-20 MPa. HTL reactions involve the depolymerization of macromolecules, thermal decomposition, and recombination processes (Mathanker et al., 2021; Gollakota et al., 2018). The decomposition phase includes dehydration, decarboxylation, and deamination of the biomass, generating furfurals, phenols, soluble organic acids, polar organic molecules, and glycolaldehydes. Repolymerization and recombination are reverse processes of depolymerization, occurring upon the loss of H2 ions which act as free radicals. In the absence of H2, previously synthesized compounds repolymerize to form coke, a robust molecular complex (Ni et al., 2022; Ravichandran et al., 2022). HTL achieves a recovery of less than 70% of its feedstock as bio-oil and BC.

The high BC yield in HTL is estimated up to 70%, but have some challenges since biomass polymers are less likely to be converted to solid phases under hydrothermal conditions compared to other thermochemical processes like pyrolysis. Research indicates that the surface area and total volume of HTL BC are generally lower than those of pyrolysis BC, regardless of the feedstock used (Guo and Rockstraw, 2007; Leng et al., 2015). The surface area ranges from 1.56 to 17 m²/g, the average pore diameter from 18 to 36 nm, and the total pore volume from 0.058 to 0.082 cm³/g (Kumar and Pant, 2015; Leng et al., 2015). Despite these differences, HTL BC retains functional groups and volatile organic matter crucial for the adsorption of metals, dyes, and other pollutants. While HTL demonstrates efficient performance, economic viability, and a high production rate, it still faces numerous operational and technical challenges that hinder its full commercialization.

Most of the above-discussed biomass-derived BC synthesis processes are less expensive, more convenient and farmer-friendly approaches than typical activation methods. A schematic representation of various BC synthesis methods can be seen in Figure 2.

Figure 2

5 Influence of BC physico-chemical soil properties

Improving soil health and adopting sustainable practices will boost crop yields, ensuring food security and environmental sustainability for the future. The impact of BC on soil properties has been widely studied. Morphological characteristics (e.g., large surface area and highly porous structure) of BC can change soil physical and chemical properties, which have been linked to changes in soil microbial community.

5.1 Impact of BC on physical properties of soil

Using BC as a soil amendment significantly increased various physical properties of soil such as BD, TP and WA.

5.1.1 Soil bulk density and total porosity

The application of BC has been shown to significantly reduce BD and increase TP by indirectly influencing soil aggregation (Li et al., 2024). This process begins with a reduction in BD, followed by enhanced soil aggregation, interaction with mineral soil particles, and ultimately decreased soil packing. Lower BD can enhance soil structure, improve nutrient release and retention, and reduce soil compaction. Similarly, higher TP provides essential space and oxygen for soil organisms, influencing the transformation, storage, and utilization of water.

Studies have indicated that BC amendment improves BD, agglomerate stability, and aggregate capacity, thereby enhancing water retention and preventing soil degradation (Wang et al., 2020b). Consistent with Zhang et al. (2012a, 2012b), the addition of 40 t ha-1 rice straw BC to the soil reduced BD from 0.1 to 0.06 g cm-3 in 2009 and 2010, while increasing rice yield by 9-12% and 9-28%, respectively. Changes in TP were observed in the 5–10 and 25 μM ranges following BC addition (Rasa et al., 2018). Furthermore, BC implementation significantly enhanced soil permeability and saturated hydraulic conductivity (Oguntunde et al., 2008).

Jeffery et al. (2011) found that BC supplements significantly enhanced crop productivity in soils with acidic pH (14%), neutral pH (13%), and coarse (10%) or medium textures (13%). Sun and Lu (2014) found that straw bulk BC significantly increased pore volume in the macropore (> 75 μm) and mesopore (30-75 μm) ranges, likely due to the reorganization of pore-size distribution and aggregation processes induced by BC addition.

Overall, the impact of BC on BD and TP is closely related to the type of BC, soil type, BC particle size, and application rate. For example, Verheijen et al. (2019) demonstrated that smaller BC particles more effectively reduced the BD of sandy soil, while larger BC particles had a greater effect on reducing the BD of sandy loam soil, indicating that various BC particle sizes can be used to achieve specific soil effects. Similarly Rasa et al. (2018) highlighted that BC chemistry and pore morphology influence BC-water interactions, thereby altering soil textures accordingly.

5.1.2 Water availability

Studies have demonstrated that BC significantly enhances WA in both sandy and clay soils (Ma et al., 2016; Pu et al., 2019). This is attributed to the porous nature of BC, which allows it to absorb substantial amounts of water, thereby altering the overall soil structure. In sandy soils, incorporating BC particles of various sizes and shapes can reduce the large gaps between soil particles (interpore spaces) and increase the proportion of micropores (5 to 30 µM in diameter) formed by the intrapores of BC. Consequently, when BC-sand mixtures become moist, the elongated shape of BC particles disrupts the grain packing in the sandy matrix, enhancing the interpore volume available for water storage (Liu et al., 2017b; Lehmann and Joseph, 2024). Applying BC at rates exceeding 3% w/w has been shown to potentially increase WA in clay soils (P < 0.05) (Kameyama et al., 2016). In a meta-analysis by Razzaghi et al. (2020) reported that BC additions increased available water content by 45% in coarse-, 21% in medium- and 14% in fine-textured soils. In clay soils, BC additions generally improve hydraulic conductivity and field capacity while reducing BD, thereby enhancing drainage, porosity, and plant-available water.

5.2 Impact of BC on chemical properties of soil

Soil chemical properties such as available N, P, potassium (K), pH, soil electrical conductivity was highly influenced by BC application.

5.2.1 Nutrient availability

The soil environment is crucial for plant growth, and BC manifestation for long time showed to enhance soil nutrient availability and improve plants’ nutrient absorption efficiency. Therefore, BC can also be utilized as a vital nutrient source for plants and soil microorganisms. The higher levels of K, N, calcium (Ca), and P available in BC render nutrients to microorganisms essential for plant growth (Sakhiya et al., 2020). Hossain et al. (2020) reported that OC and essential minerals such as Ca, K, P, N, sulfur (S), and magnesium (Mg) were elevated via BC treatment in the soil. Gao et al. (2016) found that an increased retention of NO3 N (33%) and NH4+ N (53%) has a more significant effect in the soil upon BC amendment than direct nutrient supplements. Furthermore, BC application resulted in an increased grain P (38-230%) and N (20-53%) utilization efficiency compared to N fertilizer alone (Zhang et al., 2020a).

5.2.2 Soil pH

BC application can also potentially modify common soil indicators such as pH, and electrical conductivity (Murtaza et al., 2023). Soil pH has a profound impact on plant growth and available nutrients. Generally, in agricultural fields, soil acidity (pH) increases through the application of lime to improve plant growth at maximum potential. The application of BC was found to rise the pH from 4.59 to 4.86 (Nielsen et al., 2018), from 4.8 to 6.3 (Novak et al., 2009), and from 4.3 to 4.6 (Hossain et al., 2010). Earlier studies showed that utilization of higher pH BC simultaneously increased pH in red ferralitic soil at approximately the 1/3 lime level, improved the Ca ratio and decreased Al toxicity (Glaser et al., 2002; Lehmann et al., 2003; Steiner et al., 2007). Granatstein et al. (2009) found that applying 39 t ha−1 herbaceous feedstock-derived BC to sandy soil increased the soil pH from 7.1-8.1. found a significant increase in 71% electrical conductivity and a 5.2-7.6 pH range in sandy soils treated umbrella tree-derived BC compared to untreated controls. Mostly, BC was reported to not have any effect on light and highly acidic soils (Sousa and Figueiredo, 2016). Whereas, BC significantly increase the pH value of highly acidic to light alkaline soils (; Wen et al., 2022). Moreover, some studies revealed that increasing temperature during pyrolysis process has contributed to increase in soil pH by BC (Wan et al., 2014; Karimi et al., 2020).

5.2.3 Cation exchange capacity and electrical conductivity

The CEC measures the soil’s ability to absorb, retain, and exchange cations. Enhancing the number of cation exchange sites in the soil can boost its CEC content. Soils with a high CEC are more capable of adsorbing NH4+, K+, Ca2+, and Mg2+, which enhances the efficient use of nutrient ions and minimizes nutrient loss (Liang et al., 2006). Higher CEC in soil supports plant nutrient cations binding to the clay, and humus to retain nutrients for uptake by plants instead of leaching (Glaser et al., 2002; Lehmann et al., 2003; Laird et al., 2010). After the addition of BC, the soil charge and CEC is reported to be increased by approximately 20–40% (Hossain et al., 2010). The anionic surface of BC was mainly attributed to increase the CEC of soil with both acidic and alkaline pH (). Tomczyk et al. (2020) found that woody BC enhanced the CEC of generated soil by 190% when compared with the untreated control. BC’s functional groups on the surface, silicon, alkalinity, and high pH-buffering capability contribute synergistically to moderate soil acidity (Mandal et al., 2020). The anion exchange capacity and CEC of the soil was also found to be emphasized by the incorporation of BC (Hossain et al., 2020).

5.3 Impact of BC on soil biological properties

The overall change of soil physical and chemical properties by the application of BC will result in the creation of appropriate habitat for living of beneficial microorganisms (Xu et al., 2014). In addition, due to the presence of high aromatic hydrocarbon and pore structure, BC served as a potential habitat and providing nutrient for various beneficial soil microorganism and resulted in improved crop productivity (). By increasing soil pH, BC renders the soil environment more beneficial for plant and microbes (). The micro and meso pores of BC stores water and dissolved substances required for the microbial metabolism. According to Li et al. (2022b), BC application has distinctive attributes, such as an altered strategy in root growth, enhanced enzyme activities and rhizosphere nutrient availability in soil. Plant growth regulators, karakins and other germination hormones released by BC trigger seed germination and soil physico-chemical properties (Kochanek et al., 2016). The efficacy of plant growth improvement with various BCs has been studied extensively (Table 2). The BC amendment augments soil microbial activity and diversity, which is fundamental for nutrient cycling, organic matter decomposition, and the overall health of the soil ecosystem (Hou et al., 2024). Microbial activity enhancement further aids in the stabilization of heavy metals and improves soil resilience to abiotic stresses (Pathy et al., 2020). Moreover, BC increases soil bacterial diversity and alter its structure (Huang et al., 2022).

Table 2

Plant nameBotanical nameBC feedstockPyrolysis temperatureLevel of BCEffects of BC on plant growth enhancementReferences
PumpkinCucurbita pepoMaize straw350 °C10 and 20 t ha−1Improved leaf RWCLangeroodi et al., 2019
TomatoLycopersicon esculentumCotton seed shell and rice husk400°C5% (w/w)Increased RWC and leaf photosynthetic rate
AppleMalus domesticaRice husk450 °C80 g k−1Increased seedling height, DW, respiration rate, higher root surface area, root length and root volumeWang et al., 2019
Asian lotusNelumbo nucifera Gaertn.Pinewood–10% (w/w)Increased FW of leaf, root, DW of rhizome and relative Chl contentsLiu et al., 2016
ChickpeaCicer arietinumRed sage450°C3.5 t ha-1Higher seed yield, haulm yield, and biological yieldMeena et al., 2023
Sweet basilOcimum basilicumBlack cherry wood450°C2 and 3% (w/w)Seed germination increased, improved Chl contents, enhanced surface area, total root volume and lengthJabborova et al., 2021a
GingerZingiber officinaleBlack cherry wood450°C1, 2 and 3% (w/w)Increased seed germination, leaf length, leaf number, DW of shoot and rootJabborova et al., 2021b
PeanutArachis hypogaeaMaize straw600°C10 and 20 t ha−1Photosynthesis, Chl fluorescence, and yieldWang et al., 2021
Tomato, Radish, Lettuce and Sweet pepperRaphanus sativus, Lactuca sativa and Capsicum annuumMaritime pine wood chips600°C2 kg/m2 = 10 t ha−1Increased mean FW and improved fruit and vegetable yieldGonzalez-Pernas et al., 2022
MaizeZea maysHardwood–18.4 Mg ha−1Highest grain yield and zero removal of residueRogovska et al., 2016
TeaCamellia sinensisTea plants550°C20 gHigher macronutrient contents such as N, P, and K, enhanced the leaf biomass, stem biomass, and stem diameterZou et al., 2023

Ameliorative effects of various BCs on crop growth, development and yield.

RWC, relative water content; DW, dry weight; FW, fresh weight; Chl, chlorophyll.

5.4 Decomposition properties of soil

The chemical composition in feedstock obtained from different sources affects the biological decomposition of BC (Lehmann et al., 2011). The decomposition rate was significantly higher (mean: 0.025% day 1) in crop-derived BC than (mean: 0.007% day 1) grass-derived BC as a result of lower condensed and less C content. Furthermore, wood-derived BC (mean: 0.004% day 1) contains the lowest decomposition rate due to its high C content (Hilscher et al., 2009; Knicker, 2010; Singh and Cowie, 2014). Wang et al. (2016) found that BC decomposition rates increased logarithmically over time and were significantly influenced by soil texture, clay content, biomass feedstock, pyrolysis temperature, and process duration. Limited information is known about BC degradation, and the effects on the turnover of native soil organic matter, degradation duration and other cascading effects remain unclear (Lehmann et al., 2011; ; Lorenz and Lal, 2014). Previously, the application of BC in different soils has been reviewed; however, an updated overview of the persistence, degradation, and stability of BC-amended soil is still lacking. The main reasons attributed to the paucity of decomposition of BC in soil are insufficient insight to distinguish total soil CO2 efflux from other high CO2 efflux from dead plant residues, root-derived CO2, dissolved OC, soil OM, initial BC stock, and other soil pyrogenic C (Kuzyakov et al., 2009; Wang et al., 2016).

Overall, as a soil amendment, it enhances the biological and physico-chemical characteristics of the soil, especially over a long time, enriching soil aggregation, water holding capacity (WHC), pH, and microbial activity, which enhances overall soil quality. By enhancing the soil’s organic matter content, BC can support sustainable soil management and agricultural productivity. BC acts as a multifunctional soil amendment that not only enhances the soil nutritional profile but also provides a sustainable solution to mitigate the adverse effects of salinity, drought, and heavy metal stressors on agricultural lands.

6 Soil fertility and plant growth enhancement mediated by BC

The frequent application of chemical fertilizers can eventually affect soil fertility, which in turn additionally pollutes adjacent aquatic ecosystems (Jote, 2023). BC application has been an effective way to efficiently reduce the use of synthetic fertilizers, elevate N use efficiency, and promote sustainable agriculture (Gao and DeLuca, 2016). Furthermore, BC promotes plant growth along with higher biomolecule contents, which ensures healthy plantations with nutritionally enhanced crop yields (Tan, 2023). Previously, studies have shown that the nutrient availability to plants and their retention ability in the soil have been improved through enhancing soil CEC and surface oxidation characteristics, which low native organic matter improves soil C stability upon BC amendment (Karimi et al., 2020; Singh et al., 2022). Soil augmented with BC endured higher concentrations of P, N, K, Ca, Mg, and S than untreated soils (Jin et al., 2024; ). The addition of maize residue BC at a rate of 1-2% (w/w) enhanced total N, P, K, copper (Cu), iron (Fe), manganese (Mn) and zinc (Zn) (). Similarly, the application of BC increased the total N, K and P in loamy and clay loamy soils (Nabavinia et al., 2015; Xiao et al., 2016). However, Yao et al. (2017) reported a conflicting result that the addition of maize stalk-derived BC (50 and 200 Mg ha-1) diminished total P and increased total N in soil. The combination and adequate concentration of soil mineral nutrients play a major role in the growth and development of plant species, and nutrient deficiency diminishes plant growth and yield (; Khan et al., 2024). All the reports revealed that the application of BC in soil increased the availability of both macro and micro nutrients.

Apart from improving soil quality, BC enhances seed germination and root development in various plants. For example, seed germination in sweet basil significantly increased by 28% in the 2% BC treatment and 30% in the 3% BC treatment compared with the non-BC control, which depicts a pivotal role of BC in seed germination (Jabborova et al., 2021a). However, improvement in seed germination depends on various factors, such as the type of BC feedstock, rate of BC application, plant species, soil, and other environmental conditions. BC incorporated in soil significantly improves root length, root size, surface area, root diameter, and root volume in apple, strawberry, and sweet basil compared with control plants (Wang et al., 2019; ; Jabborova et al., 2021a). Moreover, increasing (0, 5, 20, and 80 g kg-1) BC dosage application resulted in an increased root respiration of 745, 863, 960, and 1239 nmol O2 min-1 g-1 FW in apple seedlings, respectively (Wang et al., 2019).

BC application enhances plant growth regulators, seed germination, photosynthetic pigments, root growth and soil microbes, which are vital determinants of healthy plant development and productivity and synergistically improve the morphological, physiological, and biochemical properties of plants, soil enzymatic activities and soil fertility. Henceforth, BC may serve as a significant nutritional reservoir for crop development and an efficient amendment to improve soil characteristics.

7 Mechanisms of BC action in alleviating abiotic stresses in soil

Abiotic stresses significantly affect soil health and agricultural productivity. BC has emerged as a promising eco-friendly amendment for enhancing soil nutritional profiles under various abiotic stressors such as salinity, drought, and heavy metal contamination. Amendment of BC in saline soils enhances mineral nutrient, physical, chemical, and biological characteristics of the soil. BC boosts the availability of mineral nutrients and metabolism, EC, infiltration rate, BD, microbial biomass C and pH of the soil under saline-affected soils (Singh et al., 2022). BC ameliorates the adverse salinity effects by balancing WHC, porosity, and its high salt adsorption capabilities (). Specifically, in salt-stressed conditions, BC application was found to notably increase rice biomass through improving soil properties, nutrient conditions and reducing salinity indices like EC, soluble Na+, and Cl- concentrations (Huang et al., 2022). Further, BC has shown to mitigate salinity and drought stress by improving soil structure, increasing water retention capacity, and enhancing the availability of water to plants. It alters the ionic balance in soil, reducing the uptake of Na+ ions under saline conditions and thereby promoting plant growth under stress (Zhang et al., 2013).

BC aids in preserving soil nutrients by diminishing nutrient leaching, in sandy and significantly weathered soils. The higher BC surface area and porosity serve as adhesion sites for nutrients. BC augments soil CEC, substitutes detrimental Na+ ions with beneficial K and Mg ions plays a crucial role in diminishing soil salinity (). Hence, it improves retaining of vital nutrients like K, Ca, and Mg availability to plants. The alkaline pH of BC plays a significant role in neutralizing acidic soils, thereby unravelling nutrients that are naturally inaccessible in acidic environments. The application of BC enhances the soil WHC, pH, CEC and decreases BD contributing to the reduction of heavy metals’ bioavailability and the alleviation of stress caused by salinity and drought (Kumari et al., 2020; Li et al., 2021a).

By increasing the soil pH, BC renders the soil environment more beneficial for plant and microbes. The adjustment of pH facilitates the solubility of nutrients that are less available under acidic conditions, such as P, and helps in reducing the toxicity of aluminium (Al), which causes problem in low pH soils (Huang et al., 2023). BC potentially mitigates heavy metals in saline soil through increasing soil organic C, microbial and biochemical activities (). The synergy between BC and soil organic matter is pivotal for stable soil aggregates formation that facilitates root penetration and improves water infiltration. Furthermore, BC porosity enriches soil porosity, BD, soil structure and water retention that alleviates plants’ resilience to drought conditions (Mukherjee and Lal, 2013).

Immobilization of heavy metals occurs through adsorption on BC surface, complexation with functional groups, and precipitation as metal-BC complexes, thereby mitigating the toxic effects of lead (Pb), cadmium (Cd), and chromium (Cr) in contaminated soils (). BC application is crucial for restoring the productivity of soils affected by industrial pollution and mining activities. BC significantly diminishes metal uptake by plants, as evidenced by lower concentrations of metals in plant tissues.

The ability of BC to enrich nutrient retention in soil is largely attributed to its unique surface functional groups and porosity. The carboxyl, hydroxyl, and phenolic functional groups on BC’s surface are pivotal for enhancing the soil’s ability to retain nutrients, particularly under nutrient-stressed conditions (Hagemann et al., 2017; Pandit et al., 2018). BC functional groups with its porous structure significantly regulates soil P, and N retention by influencing microbial dynamics, which is vital for plant growth (Ibrahim et al., 2020; Zhang et al., 2021). BC can protect organic matter from decomposition, leading to increased soil C sequestration. This stabilization of OM contributes to the long-term improvement of soil fertility, structure, and nutrient cycling (Figure 3).

Figure 3

8 Role of BC in mitigating various abiotic stresses for plant growth and development

Abiotic stresses have been the main constraints for crop production in recent years. For several decades, plant researchers have used various techniques to mitigate abiotic stresses for plant growth and development. In recent years, many researchers have suggested that the application of BC in soil helps to alleviate different abiotic stresses and supports the enhancement of plant growth and yield. Therefore, BC is called “black gold” for agriculture. In this section, we discuss the role of BC in crop improvement under drought, salinity, and heavy metal conditions. Figure 4 is a visual demonstration of the positive impact of BC application on plants grown under normal and different abiotic stresses.

Figure 4

8.1 Salinity stress

Higher concentrations of salt in soil induce osmotic stress due to ionic imbalance, which causes severe effects on morphology, biomass, yield, and biochemical processes in plants (). Salinity stress affects over 1000 million hectares of agricultural land worldwide, making it a serious threat to agriculture (). Therefore, eco-friendly technology is urgently needed to alleviate salinity stress in soil, which helps to improve crop growth and yield. BC enhanced plant biomass, root length, root volume, yield, leaf functional traits and K+ concentration in soybean, tomato (Solanum lycopersicum) and potato (Solanum tuberosum) under salinity stress (; Farhangi-Abriz and Torabian, 2018a; She et al., 2018). Studies by , demonstrated that BC treatment improved growth, biomass and yield traits of rice as well as soil properties (including nutrients availability) under saline conditions. Kanwal et al. (2018) found that applying BC increased the length of root and shoot, leaf functional traits and osmotic potential but decreased the proline content, superoxide dismutase activity and soluble sugar upon salinity stress. BC alleviated salt stress by maintaining higher leaf relative water content (RWC) and a lower Na+/K+ ratio and further enhanced the plant growth, biomass, photosynthesis, transpiration rate and grain quality of rice, sorghum (Sorghum bicolor), maize and wheat (; Huang et al., 2019; Ibrahim et al., 2020, 2021). In another study, BC increased the plant stomatal conductance, plant yield, and chlorophyll fluorescence parameters and reduced abscisic acid in salinity stress-exposed cabbage (). In addition, BC has high salt uptake ability, thus reducing Na+ uptake in plants and mitigating the adverse impact of soil salinity (Huang et al., 2019; Yang et al., 2020).

The role of BC in response to salinity stress in plant growth and metabolism has been extensively studied (Table 3). Overall, it can be concluded that BC can be a useful strategy to alleviate the harmful effects of salinity on plant development. However, BC rates must be carefully used in saline soil to reduce saline toxicity and enhance plant growth processes. The role of BC in physiological and biochemical responses under salt stress has not been studied in many horticultural and economically important plants. Hence, initiating further experiments using BC in other horticultural and economically important plants will help to improve plant quality upon salinity stress, which may help to reduce malnutrition worldwide. Moreover, numerous salinity stress-responsive genes are involved in improving plant growth under salt stress (Golldack et al., 2011; Kumar et al., 2017). The expression pattern and role of salinity stress-related genes have not yet been identified in plants grown under salinity stress with the application of BC. Henceforth, identifying the expression pattern of salt stress-responsive genes in various tissues of plants grown under salinity stress by the application of BC helps to determine which genes are highly induced by BC under salinity stress conditions.

Table 3

Plant nameBotanical nameCultivars usedConcentration of NaClBC sourcesLevel of BCPositive and negative effects of BCReferences
PotatoSolanum tuberosumFolva25 and 50 mMCommercial charcoal5%Increased root length, root volume, tuber yield, photosynthetic rate, intrinsic water use efficiency and K+ concentration
Decreased leaf water potential, ABA content in xylem sap and leaf, Na+ concentration, leaf Chl content index, total leaf N and C content
SoybeanGlycine maxM75 and 10 dS m−1Sycamore maple plant residues50 and 100 g kg−1Increased the nodule number and weight, DW of shoot and root, total plant biomass, total plant N, GDH, GS, GOGAT, and NO3-Farhangi-Abriz and Torabian, 2017
Common beanPhaseolus vulgarisDerakhshan6 and 12 dS m−1Sycamore maple plant residues10 and 20%Increased DW of shoot and root, IAA content of roots
Decreased ABA, ACC, JA contents and Na+ content of roots and leaves
Farhangi-Abriz and Torabian, 2018c
Derakhshan6 and 12 dS m−1Sycamore maple plant residues5 and 10%Increased length of root, shoot and leaf area, DW of shoot and root, RWC, Chl fluorescence, Chl-a, Chl-b, total Chl and Chl a/b ratio and various ion concentrations (K+, Ca2+, and Mg2+) in root and shoot tissues
Decreased Na+ concentration in shoot and root tissues
Farhangi-Abriz and Torabian, 2018b
TomatoLycopersicon esculentumYazhoufenwang1 and 3 dS m−1Wheat straw2, 4 and 8%Increased photosynthesis and transpiration rate, yield, and number of fruitsShe et al., 2018
WheatTriticum
aestivum
NARC 2009 and NARC 2011150 mMWheat leaves1 and 2%Increased root and shoot length, leaf water potential and osmotic potential
Decreased proline content, SOD activity and soluble sugar
Kanwal et al., 2018
Sumai-100.3 and 10 dS m−1Wheat straw10, 20 and
30 t ha−1
Increased electrical conductivity, total above-ground biomass, grain yield, harvest index, spike and kernel number, 1000-grain weight, leaf RWC, photosynthesis rate and available P, N and K content in the soil
Decreased Na+ concentration
Huang et al., 2019
Mung beanVigna radiataMN925 and 10 dS m-1Sycamore maple plant residues50 and 100 g kg-1Increased root length, root diameter, root DW, root density, specific root length, total root area, shoot DW, shoot/root ratio, root RWC, IAA in root
Decreased ABA and ACC content in root
Nikpour et al., 2019
SorghumSorghum bicolorKambal0.26, 5.8, and 12.6 dS m-1Wheat straw2.5, 5, and 10%Increased plant height, leaf area, FW, dry matter yield, photosynthetic rate, stomatal conductance, transpiration rate Decrease activity of CAT, POD, SODIbrahim et al., 2020
Kambal0.8, 4.1 and 7.7 dS m−1Wheat straw2.5, 5, and 10%Increased shoot and root length, FW and DW of shoot and root and RWCIbrahim et al., 2021
EggplantSolanum melongenaJaylo2 and 4 dS m−1Oak and Pine tree woods5%Increased stomatal conductance, photosynthesis rate, density of root length and surface area, plant height, stem diameter, leaf area and yield
Decreased leaf temperature and electrolyte leakage in the leaf
Parkash and Singh, 2020
Bonica F1300 mMMaize straw6%Increased plant height, aerial biomass, fruit number per plant, flowering time and mean FWHannachi et al., 2023
QuinoaChenopodium quinoaTiticaca400 mMCorn straw5%Increased plant height, shoot biomass, grain yield, leaf photosynthesis, stomatal conductance, intrinsic water use efficiency and leaf K+
Decreased total leaf water potential and ABA content in leaf, leaf Chl content index, leaf N and C content and leaf Na+ content
Yang et al., 2020
RiceOryza sativaG9352.11 mMWheat straw15, 30 and 45 g per kilogramIncreased biomass, grain yield and quality
Decreased Na+ ion accumulation of various tissues
Jin et al., 2018
Changbai-923.91 dS m−Rice husk30g/kgImproved rice grain quality traits including amylose content, protein content, taste value, rough rice grain, brown rice rate, white rice rate, whiteness and transmission rate and production
Jinyuan 85 and Nipponbare1 and 3 g kg−1Rice straw–Decreased electrical conductivity, exchangeable Na+ and exchangeable Cl-Zhang et al., 2019
Changbai-9368.11 mMPeanut shell33.75, 67.5 and 102.5 t ha−1Increased leaf water status, plant height, chlorophyll content index and K+ concentration
Decreased Na+ concentration, Na+/K+ ratio and leaf-relative electrical leakage
Ran et al., 2020
Changbai-923.91 dS m−Rice husk–Increased plant height, tiller number, dry weight of leaf, panicle, stem and sheath, total dry biomass, K+ concentration and K+/Na+ ratio
Improved the concentrations of soil pH, Ca2+, Mg2+, CO32- and Cl-
Decreased Na+ concentration in different rice organs and considerably
Tianlongyou 6194.5 dS m−1Maize, wheat and peanut shell residue0.5 kg m−2Increased plant height, DW, root length, and grain yield
Reduced amylose, protein, and taste quality
Zhang et al., 2024
MaizeZea maysXianyu3352.0 and 5.0 dS m−1Wheat residue5 and 10%Increased plant height, stem diameter, number of leaves per plant, photosynthetic rate, transpiration rate, yield and nutrients N, P, and K uptake
Naudi hybrid1.25 and 2.5 g L− 1Eucalyptus residues50 and 100 g kg− 1Increased shoot and root length, DW of shoot and root, Chl a and Chl b, GSTs and CAT activitiesHelaoui et al., 2023
CabbageBrassica olerecaeYalova1150 mMCommercial charcoal2.5 and 5%Increased stem diameter, leaf area, FW and DW of root and shoot, leaf RWC, Chl a, Chl b, total Chl and plant nutrient uptake
Reduced MDA, H2O2, proline, sucrose Na and Cl content
Shanghai Green25, 50, and 100 mMCorn stover2 and 4%Increased the plant stomatal conductance, plant yield, Chl fluorescence parameters and reduced ABA

Effects of BC on plant growth and yield under salinity stress in various plants.

RWC, relative water content; DW, dry weight; FW, fresh weight; Chl, chlorophyll; ABA, abscisic acid; ACC,1-aminocyclopropane-1-carboxylic acid content; JA, jasmonic acid; IAA,indole-3-acetic acid; GDH, glutamate dehydrogenase; GS, glutamine synthetase; GSTs, glutathione-S-transferase; GOGAT, glutamine oxoglutarate aminotransferase; SOD, superoxide dismutase; CAT, catalase; POD, peroxidase; MDA, malondialdehyde.

8.2 Drought stress

One of the most important environmental factors affecting the entire plant life cycle was drought. Over 45% of the world’s cultivated land is permanently drought-prone, and 38% of the world’s population lives there (). Therefore, improving water use efficiency in plants exposed to drought stress has long been an important factor in enhancing plant growth and development (Ruggiero et al., 2017). Soil application of BC is considered as an effective practice to facilitate plant growth and yield under drought stress. Many studies have shown that the application of BC in soil increases the growth and yield of drought-stressed plants (Table 4). In tomato, BC increased the soil moisture content, photosynthetic rate, yield, quality of fruit and other biochemical traits under drought stress (; Obadi et al., 2023; Zhang et al., 2023).

Table 4

Name of the plantBotanical nameCultivars usedDrought levelBC sourcesLevel of BCPositive and negative effectsReferences
TomatoLycopersicon esculentumNo.2 Hongfen28% WHCMixture of rice husk and shell of cotton seed5%Increased the soil moisture contents, photosynthetic rate, physiology, yield, quality of fruit, RWC, membrane stability index, water use efficiency, stomatal pore aperture and stomatal density
Decreased leaf N content and Chl content index and ABA content in leaf
Tone Guitar40, 60 and 80% WHCDate palm fronds waste5%Increased plant height, leaf area index, stem diameter, and FW and DW of above-ground tissues, Chl-a, Chl-b, total Chl, Car contents, water use efficiency and fruit yieldObadi et al., 2023
Ailsa Craig70% FCWood and
poultry manure BC
5%Increased plant height, dry mass accumulation, dry root mass, dry leaf mass, ratio of root and shoot, specific leaf area, field WHC and soil water supply
Decreased ABA content in xylem sap
Zhang et al., 2023
Lady’s FingerAbelmoschus
esculentus
–60% FCLantana camara plant residues1 and 3%Increased photosynthesis, leaf area, stomatal conductance, dry matter, transpiration rate water use efficiency
Milk thistleSilybum marianum–40% WHCSycamore maple hardwood1 and 2%Increased net photosynthesis rate, water use efficiency, membrane stability index, Chl-a, Chl-b, total Chl, leaf weight, stem weight, leaf area, plant weight and plant height
Decreased internal CO2 and stomatal conductance
SoybeanGlycine maxNARC II–Corn cobs10 and 20 t ha-1Increased seedling vigor, germination percentage, rate of germination, membrane stability index of leaf, RWC, shoot length, Chl-a and Chl-b, Car and total Chl
Decreased sugar and proline content
Hafeez et al., 2017
Zhonghuang 3540–45% WHCWheat
straw
5, and 10 g kg− 1Increased water use efficiency, grain yield, root length, root and shoot biomass, photosynthetic rate, stomatal conductance and transpiration rateZhang et al., 2020b
Yeşilsoy50, 75 and 100 100% FCHazelnut shells3 and 6%Increased plant height, FW and DW of shoot and root, stem diameter, leaf area, Chl-a, Chl-b, total Chl, IAA and GA content
Reduced MDA, H2O2, proline, ABA, and sucrose content, and antioxidant activities
Gullap et al., 2024
MaizeZea maysAmadeo and DKC-339925–30% WHCWood-chip sievings1.5 and 3%Increased above-ground biomass, water use efficiency and soil NO3- contentHaider et al., 2015
ICI-891440% WHC–4 t ha−1Increased DW of shoot and root, length of shoot and root, net photosynthetic rate, transpiration rate, stomatal conductance, Chl-a, Chl-b and Chl a+bSattar et al., 2020
WheatTriticum
aestivum
Misr 150%, 75%, and 100% FCCorn stalk and rice husk1%Increased Chl-a and Ch- b, Car, RWC, grains per spike, 1000-grain weight, grain yield and harvest indexHafez et al., 2021
Glaxay 201330% WHCWheat straw27.88 and 37.18 g kg-1Increased plant height, number of fertile tillers, spike length, number of spikelets per spike, number of grains per spike and 1000-grain weightHaider et al., 2020
Galaxy-2013–Commercial charcoal28 g kg−1 and
38 g kg−1
Plant height, spike length, number of spikelet’s per spike, number of grains per spike, 1000-grain weight, grain yield per plant, N, P and K contents in soil and microbial biomassZaheer et al., 2021
Galaxy 201330%
WHC
Wheat straw3 and 5%Increased plant height, fertile tiller count, spike length, grains per spike, 1000-grain weight, yield, water use efficiency, stomatal conductance, Chl-a, Chl-b, transpiration rate, photosynthetic rate, electrolyte leakage, H2O2, SOD, CAT and PODZulfiqar et al., 2022
CabbageBrassica olerecaeYalova150%
WHC
Commercial charcoal5 and 10%Increased FW and DW of shoot and root, Chl-a, Chl-b, total Chl, leaf RWC, CAT, POD and SOD activities and nutrient uptake
Decreased H2O2, MDA and proline contents
Yildirim et al., 2021
EggplantSolanum melongenaBonica F1>30% WHCMaize straw6%Increased plant height, aerial biomass, number of fruits per plant, flowering time and mean FWHannachi et al., 2023
MelonCucumis melo–60, 85, and 100% WHCPalm leaves0.24 and 0.36 kg m-2Increased water use efficiency, FW and DW of root and shoot, root length, average fruit weight, fruit diameter, fruit flesh thickness, leaf N, Mn, K, Fe, Zn and Cu contents

Effects of BC on plant growth and yield under drought stress in various plants.

RWC, relative water content; DW, dry weight; FW, fresh weight; Chl, chlorophyll; Car, carotenoid; ABA, abscisic acid; IAA,indole-3-acetic acid; GA, gibberellic acid; SOD, superoxide dismutase; CAT, catalase; POD, peroxidase; MDA, malondialdehyde; WHC, water holding capacity; FC, field capacity.

BC application enhanced the soil moisture holding capacity, net photosynthesis rate, water use efficiency and physiological, biomass and biochemical traits in milk thistle plants exposed to drought stress (). BC ameliorates drought-stressed soybean growth from the seedling stage to yield, including seed germination and biochemical and physiological traits (Hafeez et al., 2017; Zhang et al., 2020b; Gullap et al., 2024). The combined application of BC and silicon improved biomass- and yield-related traits in maize upon drought stress (Sattar et al., 2020). BC significantly enhanced physiological, biochemical and yield traits related to drought stress tolerance in maize (Hafez et al., 2020; Haider et al., 2020; Zaheer et al., 2021; Zulfiqar et al., 2022). It has been revealed that BC treatment strengthens the defense mechanisms of drought stressed plants. As with salt-stress responsive genes, many drought-tolerant and drought-susceptible genes have been reported in plants (Kaur and Asthir, 2017; Mahmood et al., 2019). The expression pattern and role of drought-tolerant and drought-susceptible genes have not been initiated under drought stress in plants with BC amendment. Hence, in-depth molecular experiments are urgently needed to underpin the expression pattern and role of drought-tolerant and susceptible genes in plants grown under BC.

8.3 Heavy metal stress

Contamination of agricultural soil by pollutants such as heavy metals has become a growing environmental problem worldwide that affects nutrient uptake, plant growth, and metabolism. Various measures have been used to remediate heavy metal contamination from soils, including the use of metal hyper accumulator plants, organic and inorganic amendments, and agricultural practices (Maharajan et al., 2022). Among these, organic amendments are effective techniques and eco-friendly methods to reduce plant uptake of high concentrations of heavy metals from heavy metal-contaminated soils. BC can absorb heavy metals from contaminated soil and reduce their toxic effects on plants. This has been demonstrated in many plant species (Table 5). The application of cotton stalk-derived BC increased growth, biomass, transpiration rate, sub-stomatal CO2 concentrations, photosynthetic rate, chlorophyll and carotenoid contents while reducing Cd concentrations and malondialdehyde content in shoot and root tissue under Cd toxicity (Younis et al., 2016). In a study by Woldetsadik et al. (2016), the application of poultry litter, cow manure, and coffee husk BC immobilized Cd in the soil and reduced the Cd concentration in plant tissues, while BC increased the growth and uptake of P in lettuce plants. In another study, BC deduced concentrations of Cd, Cu, Pb and increased the concentrations of P, Fe and Zn in shoot and root tissues of maize (). Similarly, Miscanthus residues reduced nickel (Ni) contents in root, shoot and grains and increased the dry weight of shoot and root, photosynthetic rate, stomatal conductance, transpiration rate, yield, and several biochemical traits in maize upon Ni stress (Shahbaz et al., 2018).

Table 5

Name of the plantBotanical nameHeavy metal levelBC sourcesLevel of BCPositive and negative effectsReferences
SpinachSpinacia
oleracea
Cd (25, 50 and 100 mg kg−1)Cotton stalks3 and 5%Increased growth, biomass, transpiration rate, substomatal CO2 concentrations, photosynthetic rate, Chl-a, Chl-b, total Chl, protein and Car contents
Decreased Cd concentrations and MDA content in shoot and root tissue
Younis et al., 2016
Mn (3.779 ppm), Ni (0.331 ppm), Zn (4.88 ppm), Cr (0.138 ppm) and Mg(111.7 ppm)Cow manure and fresh sheep/goat manure3, 5 and 10%Increased the leaf area index, above-ground biomass, water use efficiency, root biomass
Reduced Ni content in leaves
Tahir et al., 2018
Pb (250 mg kg−1)Waste material of vegetables and fruits0.5%Increased FW and DW weight of root and K contents
Reduced Pb content in root
Zafar-ul-Hye et al., 2020
LettuceLactuca sativaCd (50 mg kg−1)Poultry litter, cow manure and coffee husk7%Increased plant growth, yield, and P uptake
Reduced Cd concentration
Woldetsadik et al., 2016
WheatTriticum
aestivum
Cd (2.86 mg kg−1), Zn (47.29 mg kg−1), Mn (68.31 mg kg−1) and Ni (5.33 mg kg−1)Rice straw1.5, 3.0 and 5.0%Increased plant height, spike length, root, spike, grain and shoot biomass, grain yield, photosynthetic rate, Chl-a, Chl-b, transpiration rate, stomatal conductance, water use efficiency, Zn and Mn concentrations in shoots, roots, and grains and Si content, activities of SOD, CAT in shoot and root
Decreased the Cd and Ni contents in shoot, root and grains and MDA content in shoot and root
TomatoSolanum lycopersicumCd (0.13 and 2 μg/ml)Cotton stalk1%Increased soil pH, soil electronic conductivity, soil organic matter, DW of shoot and root, length of root and stem, Chl-a, Chl-b, total Chl, anthocyanin, Car and lycopene contents
Reduced total Cd in soil, shoot Cd concentration
MaizeZea maysCu (3474 mg kg−1)
Fe (25 962 mg kg−1)
Mn (1413 mg kg−1)
Pb (1360 mg kg−1)
Zn (11 239 mg kg−1)
Cd (27.8 mg kg−1)
Date palm tree waste1, 2 and 3%Increased P, Fe and Zn concentration in shoot and root
Reduced Cd, Cu, Pb concentration in shoot and root tissue
Ni (77 mg kg−1)Miscanthus plant residues2%Increased DW of shoot and root, grain yield, photosynthetic rate, stomatal conductance, transpiration rate, CAT, APX and DHAR activities, ABA in leaves, protein, fiber, fat, starch
Reduced MDA and H2O2 activities in leaf and polyphenol, Ni contents in root, shoot and grains
Shahbaz et al., 2018
Chinese cabbageBrassica chinensisCd (41 mg kg−1)Rice straw, rice hull and maize stover1.5 and 3%Increased FW and DW of shoot and root, length of shoot, root and leaves
Reduced Cd content in shoot and root tissue
Cd (20 mg kg−1)Wheat straw5%Increased plant biomass
Reduced Cd contents in fruits
Sun et al., 2020
Chinese flowering cabbageBrassica parachinensisCd (1.19 mg kg−1)Pennisetum hydridum straws2%Increased vegetable growth, plant height, root length, root FW, above-ground FW and reduced Cd content in the roots and above ground tissuesLi et al., 2021b
SunflowerHelianthus annuusNi (77 mg kg−1)Miscanthus residues2%Increased DW of shoot and root, grain yield, photosynthetic rate, stomatal conductance, transpiration rate, CAT, APX and DHAR activities, ascorbic acid in leaves, protein, fiber, fat, starch
Reduced MDA and hydrogen peroxide activities in leaf and polyphenol, Ni contents in root, shoot and grains
Shahbaz et al., 2018
PeaPisum
sativum
Pb (1000 mg kg−1)–2%Increased DW of shoot and root, grain yield, plant height, RWC, Chl-a, Chl-b, protein, fat, fiber, carbohydrate, Fe, Zn and Mn contents, APX, SOD, CAT and DHAR activities
Reduced Pb content in root and shoot and polyphenols, MDA, H2O2 and O2
Haider et al., 2019
PeanutsArachis hypogaeaCd (1 mg kg−1)Peanut vine and rice straw5%Increased soil pH, Chl content, soluble sugars, proline, soluble protein and crude fat
Reduced Cd content in the root, above-ground tissues, shell and seed
RapeseedBrassica napusCd (0.28 mg kg−1), Cr (11.30 mg kg−1), Cu (3.60 mg kg−1), Zn (17.94 mg kg−1), Ni (1.38 mg kg−1), Pb (5.84 mg kg−1), Co (0.10 mg kg−1) and Fe (136.38 mg kg−1)Acacia nilotica woodchip1 and 2%Increased FW of shoot and root, Chl-a, Chl-b, total Chl, total pigments, Car, lycopene concentration, APX, POD and CAT activities.
Reduced Cd, Pb, Ni and Cu in soil and shoot and roots
Kamran et al., 2020
BarleyHordeum vulgareCd (1.25-1.91 mg kg−1), Cu (200-451 mg kg−1), Pb (118-211 mg kg−1) and Zn (67.2-134 mg kg−1)Miscanthus residues2%Increased shoot and root biomass and reduced Cu, Pb, Cd and Zn contents in shoot and root tissuesMedynska et al., 2020
Green pepperCapsicum annuumCd (20 mg kg−1)Wheat straw5%Increased plant biomass and reduced Cd contents in fruitsSun et al., 2020
EggplantSolanum melongenaCd (20 mg kg−1)Wheat straw5%Increased plant biomass and reduced Cd contents in fruitsSun et al., 2020

Effects of BC on plant growth and yield under heavy metal stress in various plants.

DW, dry weight; FW, fresh weight; Chl, chlorophyll; Car, carotenoid; ABA, abscisic acid; APX, ascorbate peroxidase; DHAR, dehydrogenase reductase; SOD, superoxide dismutase; CAT, catalase; POD, peroxidase; MDA, malondialdehyde.

BC derived from wheat straw increased plant biomass and reduced Cd contents in fruits of green pepper and eggplant (Sun et al., 2020). Overall, BC could be effective in immobilizing heavy metals in the soil and reducing heavy metal uptake and accumulation in plant tissues. In general, HM uptake by roots is facilitated by various metal transporters (Maharajan et al., 2022). However, the role of heavy metal transporters has not yet been reported in BC-treated plant tissues. Hence, environmental researchers should collaborate with plant molecular biologists to initiate in-depth molecular experiments in this field, which may help to understand the accurate role of BC in plant growth and yield. Apart from this, BC derived from heavy metal accumulator plant residues has not yet been used for any experiments. Hence, researchers can try to derive BC from heavy metal accumulator plant tissues and apply them to identify the effect of BC on plant growth and yield.

9 Conclusion and future perspectives

The utilization of BC, derived from agricultural and forestry residues, aligns with global sustainability goals by converting waste materials into valuable resources that enhance agricultural output. Synthesis techniques, BC processing, soil amendments, and applications to alleviate abiotic stressors in plants have received a lack of research attention. Hence, this review compiles the conversion of residual biomass into valuable BC amendments for soil and crop improvement upon abiotic stressors. Due to the post pandemic financial crisis, low-cost soil amendments are mandatory to increase crop production to overcome worldwide food scarcity. BC application is a promising strategy to promote soil–plant enrichment for the production of highly nutritious crops and yields, ameliorate plant abiotic stresses, controlled usage of hazardous synthetic fertilizer-based soil amendments to enhance sustainable agriculture. BC has a positive impact on soil structure, quality, and physico-chemical properties such as BD, pH, CEC, porosity, nutrient balance, WHC, and aeration. The optimal ratio of BC formulations has been potentially enriching yields under plant- and soil-specific constraints, limited water, nutrients and adverse conditions. Also, offering a promising avenue for enhancing global food security and environmental health. The recommended dosage of BC for quality improvement under specific soil and plant species is not yet well defined. Moreover, research must be focused on BC at low doses, and high efficacy is crucial to maximize farmer-friendly, cost-effective BC applications for several cropping systems.

The synergistic effects of BC along with compost, fertilizers and beneficial soil microbes that stimulate crop growth and soil fertility remain unclear. Although, long-term BC risk management and life cycle assessments are not yet completely clarified. The discrepancy between field and laboratory experiments regarding physico-chemical properties, soil quality, abiotic stress, environmental impacts, and plant growth efficiency should be scrutinized. BC production parameter optimization, functionalization, elucidation of BC augmenting mechanisms, integration of multi-omics technologies, data-driven and machine learning methods would contribute to BC applications for soil fertility and cost-effective high-yielding production of valuable crops in sustainable agricultural management. While initial production and application costs can be high, the long-term savings, enhanced crop resilience, and potential carbon credits make BC a viable option. However, further technological advancements and policy support are essential to encourage broader adoption. As per our knowledge, physiological and biochemical modifications by BC under abiotic stress have been identified, while molecular identification and characterization in this field remain underexplored. These areas of research should be prioritized by plant and environmental scientists, as they could provide deeper insights into plant development, food security, and sustainable agricultural practices. In summary, increasing soil health along with sustainable crop productivity and profitability under challenging environmental conditions can be significantly influenced by BC soil amendment technologies. Moreover, additional investigation is required to implement the machine learning approach on BC-based soil amendment, the alleviation of abiotic stress for sustainable crop production, soil fertility management, and hence light up BC industrialization.

Statements

Author contributions

PR: Formal analysis, Investigation, Resources, Software, Writing – original draft. TM: Data curation, Visualization, Writing – original draft. RJ: Writing – review & editing. MP: Writing – review & editing. IL: Data curation, Investigation, Resources, Writing – review & editing. PY: Data curation, Investigation, Resources, Writing – review & editing. SJ: Funding acquisition, Project administration, Supervision, Writing – review & editing.

Funding

The author(s) declare financial support was received for the research, authorship, and/or publication of this article. This work was supported by the “Cooperative Research Program for Agriculture Science and Technology Development (Project No. RS-2020-RD008517)” Rural Development Administration, Republic of Korea. This work was supported by the 2023 RDA Fellowship program of the National Institute of Horticultural and Herbal Science, Rural Development Administration, Republic of Korea.

Acknowledgments

We would like to express sincere gratitude to Dr. Subramani Pandian, Dr. Pandian Muthuramalingam, Dr. Subramanian Muthamil and Dr. Jayabalan Shilpha for helping during the study.

Conflict of interest

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

Publisher’s note

All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article, or claim that may be made by its manufacturer, is not guaranteed or endorsed by the publisher.

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Summary

Keywords

abiotic stress, biochar (BC), BC synthesis, crop improvement, soil properties, soil stress alleviation

Citation

Rathinapriya P, Maharajan T, Jothi R, Prabakaran M, Lee I-B, Yi P-H and Jeong ST (2025) Unlocking biochar impacts on abiotic stress dynamics: a systematic review of soil quality and crop improvement. Front. Plant Sci. 15:1479925. doi: 10.3389/fpls.2024.1479925

Received

13 August 2024

Accepted

20 December 2024

Published

13 January 2025

Volume

15 - 2024

Edited by

Rabia Nazir, Pakistan Council of Scientific & Industrial Research, Pakistan

Reviewed by

Alio Moussa Abdourazak, Abdou Moumouni University of Niamey, Niger

Romina Alina Marc, University of Agricultural Sciences and Veterinary Medicine Cluj-Napoca, Romania

Mjv Largia, St.Xavier’s College, India

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*Correspondence: Seung Tak Jeong,

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All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article or claim that may be made by its manufacturer is not guaranteed or endorsed by the publisher.

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