Abstract
Purpose
Forests play a critical role in terrestrial ecosystem carbon cycling and the mitigation of global climate change. Intensive forest management and global climate change have had negative impacts on the quality of forest soils via soil acidification, reduction of soil organic carbon content, deterioration of soil biological properties, and reduction of soil biodiversity. The role of biochar in improving soil properties and the mitigation of greenhouse gas (GHG) emissions has been extensively documented in agricultural soils, while the effect of biochar application on forest soils remains poorly understood. Here, we review and summarize the available literature on the effects of biochar on soil properties and GHG emissions in forest soils.
Materials and methods
This review focuses on (1) the effect of biochar application on soil physical, chemical, and microbial properties in forest ecosystems; (2) the effect of biochar application on soil GHG emissions in forest ecosystems; and (3) knowledge gaps concerning the effect of biochar application on biogeochemical and ecological processes in forest soils.
Results and discussion
Biochar application to forests generally increases soil porosity, soil moisture retention, and aggregate stability while reducing soil bulk density. In addition, it typically enhances soil chemical properties including pH, organic carbon stock, cation exchange capacity, and the concentration of available phosphorous and potassium. Further, biochar application alters microbial community structure in forest soils, while the increase of soil microbial biomass is only a short-term effect of biochar application. Biochar effects on GHG emissions have been shown to be variable as reflected in significantly decreasing soil N2O emissions, increasing soil CH4 uptake, and complex (negative, positive, or negligible) changes of soil CO2 emissions. Moreover, all of the aforementioned effects are biochar-, soil-, and plant-specific.
Conclusions
The application of biochars to forest soils generally results in the improvement of soil physical, chemical, and microbial properties while also mitigating soil GHG emissions. Therefore, we propose that the application of biochar in forest soils has considerable advantages, and this is especially true for plantation soils with low fertility.
Similar content being viewed by others
Explore related subjects
Discover the latest articles, news and stories from top researchers in related subjects.Avoid common mistakes on your manuscript.
1 Introduction
Mitigating increases in atmospheric CO2 concentration is an area of growing importance and concern. More detailed understanding of how carbon cycles through various sources and sinks in different ecosystems is needed at the global scale. Forests play a key role in terrestrial ecosystem carbon cycling (Fang et al. 2001; Zhou et al. 2006b; Wood et al. 2012). The total forest area in the world decreased from 4.28 to 3.99 billion hectares from 1990 to 2015, while the area of plantation forests increased from 167.5 to 277.9 million hectares over the same time period (Payn et al. 2015). Thus, sustainable management of plantation forests is of significance for enhancing the carbon sink capacity of forest land and mitigating global climate change.
The sustainable management of plantations is affected by many climatic and environmental factors. For example, soil acidification resulting from increased nitrogen deposition plus other negative effects of global warming on soil properties and plant growth hamper the sustainable management of plantations (Bai et al. 2015; Bussotti et al. 2015). While management practices can promote the growth and productivity of forests, they can also negatively affect soil ecology (Hedwall et al. 2014). For example, management practices that were used in intensively managed Moso bamboo forests, including fertilization, tillage, and understory removal, significantly decreased soil microbial biomass C (MBC) compared to natural bamboo forests (Zhou et al. 2006a). Further, intensive management such as heavy fertilization and mulching of a Lei bamboo plantation significantly decreased the diversity of carbon sources available to microbial communities reducing native microbial diversity (Xu et al. 2008). Moreover, previous studies have demonstrated that long-term intensive management, including fertilization, tillage, and understory removal, significantly reduced the size of the total and labile organic carbon stocks in Moso bamboo and Chinese chestnut plantations (Li et al. 2013, 2014). The development of sustainable management practices, which enhance plantation productivity while impeding the degeneration of natural soils, is required.
One example of such sustainable management practices may be the application of biochar. Biochar is produced from the pyrolysis of biomass under oxygen-limited conditions (Lehmann 2007; Wu et al. 2012). Over the past decade, a considerable amount of research has demonstrated that biochar can improve soil physical properties, increase soil carbon storage capacity, stabilize soil organic carbon pools (Wang et al. 2014a), improve soil biological properties (Luo et al. 2013; Dong et al. 2015), and reduce greenhouse gas emissions (Dong et al. 2013; Gul et al. 2015; Deng et al. 2017). Thus, biochar application to forest ecosystems may be a way to restore plantation productivity in the face of global climate change and intensive management (Lehmann 2007; Stavi and Lal 2013). The majority of studies on the environmental (Wang et al. 2010; He et al. 2015, 2016a; Zhang et al. 2014, 2016a, b; Lu et al. 2014a, 2017; Yang et al. 2016, 2017; Qi et al. 2017; Yuan et al. 2017; Huang et al. 2018; Niazi et al. 2018; Xu et al. 2018) and ecological consequences of biochar application on soils have been conducted on agricultural (Wang et al. 2011; Zhang et al. 2012, 2013, 2017; Prayogo et al. 2014; Xu et al. 2015) or grassland soils (Scheer et al. 2011; Slavich et al. 2013). In contrast, the effects of biochar application on soil properties and related ecological processes in forest ecosystems have not been fully resolved. A recent review (Luo et al. 2016) summarized research on the distribution of forest wildfires and the resulting concentration and characteristics of biochar produced through these wildfires as well as its influence on soil processes. The amount of biochar produced by wildfires is estimated to be 116–385 Tg C annually (Santin et al. 2015). It results from incomplete combustion and equates to about 1% of the global aboveground plant biomass in forest ecosystems (Ohlson et al. 2009; Luo et al. 2016). Here, we review the effects of biochar applications on soil properties and processes in forest ecosystems. First, we review the effect of biochar application on the soil physical, chemical, and biological properties in forest ecosystems. Second, we discuss the potential for reducing greenhouse gas emissions via biochar application to plantations. Finally, we outline the prospects for future research concerning biochar application in forest ecosystems. The general effects of biochar application on the properties and functions in forest soils are presented in Fig. 1. In brief, when biochar is applied to forest soils, it will directly/indirectly influence soil physical and chemical properties, which will affect the soil microbial abundance, composition, and functions. The changes in the soil physical, chemical, and biological properties in turn will affect greenhouse gas emissions. The aim of this review is (i) to critically discuss the impacts of biochar application on forest soils and the mechanisms involved, and (ii) to advance the development of technologies for soil quality management and the sustainable development and management of forest soils.
2 Biochar characteristics
Biochar is produced through pyrolysis. It is carbon-rich and has a high proportion of aromatic C (Gul et al. 2015) and high chemical and biological stability (Lehmann 2007). In general, biochar has a high porosity, a large specific surface area and adsorption ability, as well as a high cation exchange capacity (Luo et al. 2016). The elemental composition of biochar generally comprises in most cases more than 60% C, N, H, and other nutrient elements including K, Ca, Na, and Mg at lower concentrations (Gul et al. 2015).
The characteristics of biochar are mainly affected by feedstock type and pyrolysis temperature (Manyà 2012; Gul et al. 2015). In general, biochar derived from manures, seaweeds, and crop residues have a higher pH, a higher concentration of nutrients and less stable C compared to that derived from feedstocks with higher contents of lignocellulosics such as wood (Kloss et al. 2012; Gul et al. 2015). Additionally, biochar produced from wood biomass usually has a higher surface area than that produced from grass biomass (Mukherjee et al. 2011; Zhao et al. 2013). As to the effects of pyrolysis temperature, it has been reported that biochar produced with relatively high (600–700 °C) temperatures, leads to higher proportions of aromatic C and lower proportions of H and O functional groups, and consequently to a lower cation exchange capacity (Novak et al. 2009; Uchimiya et al. 2011; Ahmad et al. 2014). On the other hand, biochar produced with relatively low (300–400 °C) pyrolysis temperature has leads to a higher proportion of C-O and C-H functional groups and consequently a higher cation exchange capacity (Glaser et al. 2002; Novak et al. 2009).
3 Effects of biochar on soil physical properties
Soil physical properties, mainly including bulk density, soil structure, water holding capacity and aggregate formation and stability, directly/indirectly influence the retention, movement and availability of soil nutrients as well as soil microbial activity, and consequently affect plant growth (Alameda et al. 2012; Cardoso et al. 2013; Nawaz et al. 2013; Hartmann et al. 2014; Kormanek et al. 2015; Heydari et al. 2017). Forest clear cutting, converting natural forests into plantations, and the intensive management of plantations have been shown to deteriorate soil physical health, i.e., increasing bulk density, reducing porosity, and deteriorating soil structure (Jorge et al. 2012; Kleibl et al. 2014; Sankura et al. 2014; Chang et al. 2017; Tonks et al. 2017). Finding a cost-effective way to counteract these undesirable effects of forest plantation management on soils is critical. Due to the typical characteristics of biochar including its high porosity, low density, and high surface area, biochar application generally decreases soil bulk density, while increasing soil porosity, water holding capacity, and aggregate stability (Fig. 1). In the following section, we discuss the effects of biochar application on soil physical properties in forest ecosystems and the mechanisms involved.
3.1 Soil bulk density
Biochar can effectively reduce soil bulk density, and this has been demonstrated in a wide variety of agricultural soils of differing textures (Artiola et al. 2012; Abel et al. 2013; Basso et al. 2013; Herath et al. 2013; Castellini et al. 2015; Burrell et al. 2016). In comparison, reports on biochar effects on the bulk density of soils under forests are scarce. A few case studies showed effects comparable to those observed in agricultural systems (Prober et al. 2014; Mertens et al. 2017). For example, Prober et al. (2014) reported that soil bulk density was significantly lower on plots treated with a greenwaste biochar at a rate of 20 t ha−1 in mesic woodlands after 2 years compared to the control. The authors attributed the observed decrease to the incorporation of the low bulk density biochar material into the soil (Prober et al. 2014).
However, in other studies, biochar application had no significant effect on bulk density. Mertens et al. (2017) showed that Prosopis juliflora-biochar application did not significantly affect the soil bulk density of a sandy soil planted with seedlings of Spondias tuberosa Arruda. The authors hypothesized that this lack of effect was due to the low number of pyrogenic nanopores of the biochar, which could be explained by the low pyrolysis temperature used in their experiment. In conclusion, it should be noted that differences in biochar materials, pyrolysis processes, application rates, and soil types present in different forest systems will affect changes in soil bulk density. The large difference between root growth of forest plants and agricultural crops necessitates further study regarding the influence of biochar on soil bulk density in forest ecosystems.
3.2 Soil porosity
Numerous studies have shown that the application of biochar can improve soil porosity and structure, and consequently increase the water holding capacity of soils and improve nutrient bioavailability (Moyano et al. 2013; Gul et al. 2015), which promotes plant growth (Xiao et al. 2016a; Obia et al. 2016). Soil pores can be classified into the following five categories according to their equivalent pore diameter (EPD): macropores (75–100 μm), mesopores (30–75 μm), micropores (5–30 μm), ultramicropores (0.1–5 μm), and crytopores (0.1–0.007 μm) (Cameron and Buchan 2006). The pore size distribution affects aeration, water holding capacity, and drainage capacity of soils.
Recent studies have demonstrated that the effects of biochar application vary with differences in soil pore characteristics (Hseu et al. 2014; Lu et al. 2014b; Sun and Lu 2014). For example, Hseu et al. (2014) reported that the abundance of macropores, defined in this study as pores with a diameter > 75 μm, increased by 4 to 27% in mudstone slopeland soils after rice husk biochar application (2.5, 5, and 10%, w/w) and incubation for 168 days at 28 °C and 60% water holding capacity. The authors reasoned that this result could be attributed to soil particle rearrangement. They also found that micropores, defined as pores with diameters between 5 and 30 μm, increased from 11 to 54%. Similarly, Lu et al. (2014b) found that the application of rice husk biochar (2, 4, and 6%, w/w) significantly increased the porosity of clayey soils. The authors hypothesized that the increase in macropore volume (> 75 μm) was due to the biochar’s high abundance of macropores. Further, addition of straw biochar, woodchips biochar, and wastewater-sludge biochar increased the total soil porosity in a clayey soil (Vertisol) by 29, 12, and 16%, respectively (Sun and Lu 2014). The results from this study confirm that the pore structure of biochar greatly influenced the effect of biochar on soil pore structure (Sun and Lu 2014).
Despite the abundance of biochar studies on soils, little analyses have been conducted on forest soil porosity. Pore size distribution in forest soils is influenced by soil biological properties, vegetation, and forest management methods. Therefore, it is critical to quantitatively assess the pore size distribution of forest soils, for example, by using X-ray computed tomography in order to predict the structural transformation of these soils upon biochar addition. Studies to this effect will help to better understand the changes in soil processes induced by biochar application and provide an important basis for future soil improvement and enhanced forestry production.
3.3 Soil water holding capacity
Forest soils act as moisture reservoirs and regulators in the forest water cycle. Numerous studies have shown that soil water stress affects the growth of natural and planted forests and increases tree mortality (Brzostek et al. 2014; Fargeon et al. 2016). Recent studies have demonstrated that the application of biochar can significantly increase soil water holding capacity and thus moisture contents in forest ecosystems. For example, Prober et al. (2014) reported that the soil moisture content in mesic woodlands increased by 6 to 25% after the application of greenwaste biochar at a rate of 20 t ha−1. Similarly, Li et al. (2017b) reported that the overall average runoff decreased by 28% after the application of rice straw biochar at a rate of 20 t ha−1 over a period of 2 years, compared to a control treatment. The reduction in runoff was attributed, inter alia, to the strong water retention effect of biochar.
In addition, the response of soil hydrological properties to biochar applications is biochar-specific (Lewis et al. 2006; Mukherjee and Lal 2013). For example, Uzoma et al. (2011) investigated the effects of biochar application at various rates (0, 10, and 20 t ha−1) and biochar pyrolysis temperatures (300, 400, and 500 °C) on the hydraulic properties of sandy soils. The experiments indicated that biochar application increased the saturated water content from 0.2 to 56.1%. The application of biochar significantly increased the available water capacity of all treated sandy soils compared to the control except for the treatment with biochar prepared with a pyrolysis temperature of 300 °C and an application rate of 10 t ha−1. In addition to biochar specificity, the response of soil hydrological properties to biochar amendments is soil-specific (Lewis et al. 2006). For example, biochar treatment significantly increased the water holding capacity of sandy soils, but no such effect was observed for silt loams despite equivalent water potentials (Tian et al. 2015). In conclusion, the water holding capacity of forest soils plays an important role for forestry production, especially in arid and semi-arid areas. It is critical to further study the effects of different biochar types on the water holding capacity and plant available soil water contents of different soil types and under different forest ecosystems, as well as the associated mechanisms.
3.4 Soil aggregation
In general, the application of biochar has been shown to positively affect soil aggregate characteristics (Ding et al. 2016). For example, Lei and Zhang (2013) reported that in an incubation experiment with a loamy soil biochar addition (5%, w/w) significantly promoted the formation of macro-aggregates and enhanced the stabilization of macro-aggregates in the first 30 days. Lu et al. (2014b) similarly found that the addition of rice husk biochar (2, 4, and 6%, w/w) increased soil aggregation by 8–36% in a clayey soil (Vertisol). Likewise, Ouyang et al. (2013) found that the addition of dairy manure biochar (2%, w/w) significantly promoted the formation of macro-aggregates in both a silty clay soil and a sandy loam soil. In addition to the above studies, field and incubation studies have demonstrated enhanced soil aggregation through biochars, produced at pyrolysis temperatures between 400 and 600 °C, in sandy loam to clay loam textured soils (Ibrahim et al. 2013; Mukherjee and Lal 2013; Khademalrasoul et al. 2014; Soinne et al. 2014).
The mechanisms underlying the increased aggregate formation and stability due to biochar can be explained by several processes:
-
1.
The physical and chemical nature of biochars affects soil aggregation formation. For example, the first step in the process of soil aggregate formation and stabilization, the binding of biochar to organo-mineral complexes, is affected by the surface area of the biochar and its O/C ratio (Gul et al. 2015). This mechanism is supported by the observation that biochar produced at high temperature (700 °C) with a low O/C ratio did not change the aggregation characteristics of a coarse-textured soil (Busscher et al. 2010, 2011).
-
2.
The carboxyl groups formed by the surface oxidation of biochar can complex with soil minerals, and thereby enhance the stability of soil aggregates (Glaser et al. 2002).
-
3.
Biochar application increases root biomass and root activity, thus favoring fungal growth, which will enhance the stability of soil aggregates (Bossuyt et al. 2001; Bruun et al. 2014).
-
4.
Lastly, biochar treatment increases soil hydrophobicity, and consequently, decreases the extent of clay swelling and aggregate disruption, thereby improving the stability of soil aggregates (Lu et al. 2014b).
In contrast to the above studies, others have shown that biochar application had no significant effect on aggregate stability. For example, Busscher et al. (2010) reported that the addition of walnut shell biochar at a rate of 0, 5, 10, and 20 g kg−1 (incubated at 10% soil moisture content at temperatures ranging from 17 to 27 °C) had no significant effect on the stability of the aggregates in a loamy sand. Likewise, Peng et al. (2011) reported that the addition of 1% straw biomass carbon (incubated in a darkened room of 25 °C, 40% field capacity) had no significant effect on the stability of soil aggregates in Ultisol soils in southern China. The authors attributed the no effect of biochar application on the soil aggregation to the fact that the biochar did not produce aggregating exudates during its mineralization (Peng et al. 2011). Thus, the biochar processing parameters, soil type, and climate conditions can all significantly influence the effect of biochar on soil aggregates (Burrell et al. 2016).
4 Effects of biochar on soil chemical properties
The growth and production of forests are closely associated with soil chemical properties, such as pH, cation exchange capacity (CEC), organic C pool, and nutrient status. Recently, long-term intensive plantation management, mainly including chemical fertilization and understory removal, has been reported to decrease soil pH and deplete plantations’ soil organic C pools (Li et al. 2013, 2014), which negatively affect the growth of forest plants (Lapenis et al. 2004; Ito et al. 2011; Lorenz and Lal 2014). Biochar addition can directly influence soil chemical properties (Fig. 1), since it is an alkaline material containing various mineral elements and a large proportion of carbon with highly aromatic structures, as well as a large number of functional groups, such as COO−, on its surface (Lehmann et al. 2011; Luo et al. 2016). In addition, biochar application will affect soil nutrient availability and transformation indirectly through altering soil physical properties (Gul et al. 2015). In the following sections, we discuss the effects of biochar application on different soil chemical properties and the mechanisms involved.
4.1 Soil pH
Increased soil pH as a result of biochar application has been extensively investigated in agricultural soils (Jeffery et al. 2011; Gul et al. 2015), and similar results have been found in forest soils (Wang et al. 2014b; Wrobel-Tobiszewska et al. 2016). For example, Wrobel-Tobiszewska et al. (2016) found that high rates of biochar application (50–100 t ha−1) increased soil pH from 4.0 to 4.8 in a Eucalyptus forestry plantation. Further, Rhoades et al. (2017) reported that the joint application of biochar (application rate of 20 t ha−1) and mulch (application rate of 37 t ha−1) increased soil pH from 5.7 to 6.4 in a lodgepole pine (Pinus contorta) forest, while the application of either biochar or mulch alone had no pH effect. Our previous results (Wang et al. 2014b) showed that the application of bamboo leaf biochar (application rate of 5 t ha−1) significantly increased soil pH in an intensively managed Chinese chestnut plantation grown on a Ferrasol. There are two possible mechanistic explanations for the observed increases in soil pH as a result of biochar application. First, biochar is alkaline and contains mineral carbonates with an abundance of basic-charged groups (Yuan and Xu 2011). Thus, the observed increase in soil pH may be simply due to the addition of alkaline material. Alternatively, biochar application decreases the exchangeable aluminum content of soils through binding Al3+ ion by oxygenated functional groups on its surface, thereby increasing the abundance of soil exchangeable base cations, increasing soil base saturation, and ultimately resulting in a soil pH increase (Yuan and Xu 2011; Yuan et al. 2011; Dai et al. 2017). However, these mechanisms require further investigation as some studies have shown no pH effect of biochar application to forest soils (Noyce et al. 2015; Sackett et al. 2015; Mitchell et al. 2016). These contrasting findings among different studies may be attributed to differences in biochar feedstock, the pyrolysis process, and distinct soil properties in addition to those of the local environment (Dai et al. 2017).
Biochar has recently gained attention as an excellent alternative to lime amendment, which is the most commonly used method of increasing soil pH (Dai et al. 2017). Biochar has the additional advantage over lime amendment of enhancing soil carbon sequestration. In contrast, lime decomposes after incorporation into soils, and subsequently is one of the primary sources of soil CO2 emissions (West and McBride 2005). Biochar, on the other hand, can play a role in mitigating soil greenhouse gas emissions (discussed in the following section). The utility of various biochars for increasing soil pH necessitates research into the optimization of biochar production for lime-like effects.
4.2 Soil organic carbon pools
Increasing soil organic carbon levels by incorporating biochar into soils may be an effective way to mitigate soil organic carbon depletion in intensively managed ecosystems. Laird et al. (2010) showed that soil organic carbon content in a Clarion soil (Mesic Typic Hapludolls) increased with the addition of biochar after adding 0, 5, 10, and 20 g kg−1 biochar to soils. Further, our investigation (Wang et al. 2014b) showed that biochar application at a rate of 5 t ha−1 significantly increased soil organic carbon storage in a Chinese chestnut plantation, but addition of bamboo leaf with an equivalent amount of organic carbon did not have a comparable effect. Potentially, the primary reason for these observations is that the carbon present in biochar is stable and difficult to decompose in soil environments, thus contributing to the recalcitrant soil carbon pool (Lorenz and Lal 2014). Hamer et al. (2004) reported that the decomposition rates of biochar (10%, w/w) made from corn straw, rye straw, and wood were 0.78, 0.72, and 0.26%, respectively, after incubation for 60 days (20 °C, 60% of water holding capacity). Moreover, Kuzyakov et al. (2009) used 14C-labeled ryegrass to produce biochar, and found that only 1.8–2.1% of the biochar was decomposed after 60 days of incubation. These results point to the long-term stability of biochar-amended carbon in soil environments. However, it is necessary to investigate longer-term effects of biochar applications on the soil carbon pool and subsequent transformations in future studies.
Biochar application also impacts the labile fractions of the organic carbon pools in soils (Luo et al. 2011; Lorenz and Lal 2014). Wang et al. (2014b) reported that biochar application significantly increased the concentrations of soil water-soluble organic carbon and MBC in a Chinese chestnut plantation in the first month after application. Such short-term effects can probably be attributed to the release of oil condensates that are formed during pyrolysis (Smith et al. 2010). However, the effects of biochar application on soil labile organic carbon significantly differ depending on soil types. For example, Durenkamp et al. (2010) found that the application of biochar increased soil MBC content in clay soils, while it decreased soil MBC content in sandy soils. Moreover, others have found that the effect of biochar application on soil labile organic carbon was dependent on the time elapsed since the biochar application. For example, Hua et al. (2012) reported that coconut shell biochar application initially increased the soil labile organic carbon, but this effect gradually decreased with time.
4.3 Soil cation exchange capacity
Biochar application generally increases soil CEC, which improves plant nutrient availability and is thus beneficial for plant growth (Atkinson et al. 2010; Lorenz and Lal 2014). Glisczynski et al. (2016) found that the application of 30 t ha−1 biochar-compost substrates significantly increased soil CEC in poplar, willow, and alder tree plantations grown on a Luvic Stagnosol (Episiltic). Further, Cheng et al. (2008) reported that the incubation (30 °C and 60% of water holding capacity) of oak biochar over 1 year increased soil CEC from 1.7 to 71.0 mmol kg−1, which is likely because of the continuous oxidation of functional group on the surface of the biochar surface and the adsorption of organic acids by the biochar. The authors also suggested that soil CEC will further increase over time in the biochar-amended treatments. In contrast, Novak et al. (2009) demonstrated that the application of walnut shell biochar (pyrolysis temperature of 700 °C) had no significant effect on the CEC of acidic sandy soils. Reasons might have included the short experimental time (120 days) and the low oxidation extent of the biochar used.
The increase in soil CEC resulting from biochar applications can be explained via two possible mechanisms. First, biochar adsorbs soil organic matter and other compounds, and this capacity increases with the degree of biochar oxidation. Adsorption to biochar increases charge density, and consequently enhances soil CEC (Liang et al. 2006; Lee et al. 2010; Van Zwieten et al. 2010a). Second, biochar gradually oxidizes after its application to soil, and as a consequence, aromatic rings are replaced by COO− functional groups, and the overall surface negative charge increases on the biochar, thereby enhancing soil CEC (Mao et al. 2012). Fresh biochar generally has far fewer COO− constituents and a lower CEC compared to oxidized biochar, which supports the above argumentation (Brewer et al. 2009; Nguyen et al. 2010).
The chemical composition and structure of biochar can significantly affect its capacity to improve CEC (Van Zwieten et al. 2010a; Mao et al. 2012). Lee et al. (2010) found that the biochar O/C ratio is related to soil CEC capacities. Higher O/C values indicate a higher hydroxyl group content, where carboxylates and carbonyl groups of biochars improve soil CEC. The physical and chemical properties of biochars are closely related to pyrolysis temperatures (Angın et al. 2013). For example, higher pyrolysis temperatures (e.g., 600 °C) resulted in a greater surface area and consequently reduced charge density, leading to a lower CEC, in addition to fewer volatile compounds (Lehmann et al. 2011), which also contributed to the overall negatively charged components. Further, Wang et al. (2017) proposed that increasing pyrolysis temperatures leads to a loss of functional groups, which thereby decreases biochar CEC. In addition to the above, the effect of biochar application on soil CEC is dependent on soil type. For example, biochar application resulted in larger CEC increases in acidic soils than in calcareous soils (Liang et al. 2006; Gul et al. 2015).
4.4 Soil nutrient availability
Biochar application is thought to increase the inorganic nutrient content and bioavailability since biochar itself also contains various inorganic constituents (Biederman and Harpole 2013). Biochar produced from wood waste materials generally contains high levels of soluble potassium and variable concentrations of phosphorus and calcium (Page-Dumroese et al. 2015). Sackett et al. (2015) showed that bioavailable potassium concentrations significantly increased in the initial period (2–6 weeks) after maple biochar application at a rate of 5 t ha−1 in a northern hardwood forest soil, while the concentrations of available calcium and magnesium increased 9 to 12 months following application. In addition, Gundale et al. (2016) reported that biochar application at a rate of 10 t ha−1 in a boreal forest increased the soil’s net N mineralization rate and NH4 + concentration after two growing seasons. Other studies have shown that biochar application increased other nutrient concentrations including silica, boron, and molybdenum (Kloss et al. 2014; Liu et al. 2014). Kloss et al. (2014) found that biochar application (3%) in a greenhouse pot experiment significantly increased boron and molybdenum availability for three different soil types (Planosol, Cambisol, and Chernozem).
The amount and type of nutrients present in biochar is related to the feedstock type (Gaskin et al. 2008) in addition to pyrolysis temperature and duration (Tsai et al. 2007), indicating that different biochar types will affect nutrient enhancement in different ways. Moreover, increases in soil nutrients caused by biochar application are generally short-lived, and such effects decline with time due to plant uptake and leaching (Topoliantz et al. 2005; Steiner et al. 2007; Gaskin et al. 2010). Lehmann et al. (2003) proposed that the immediate beneficial effects of charcoal application on plant growth and yield in tropical soils can be attributed to the increased bioavailability of Ca, Cu, K, P, and Zn. However, the effect of biochar application on plant growth and yield over the long term is mainly due to modifying nutrient bioavailability rather than via the direct supply of nutrients from biochar (Glaser et al. 2002). For example, biochar application increased phosphorous and potassium retention through adsorption to its large and porous surface, and consequently decreased nutrient leaching losses. This process increased the concentrations of available phosphorous and available potassium in the soil, which then increased plant growth and yield (Biederman and Harpole 2013). In summary, a combination of biochars and chemical fertilizers is needed to ensure sustainable forest management in the long term, as nutrients in biochar alone are not sufficient to maintain the growth of plantation trees.
5 Effects of biochar on soil microbial properties
The above discussed changes in soil physical and chemical properties caused by biochar application will also change soil microbial properties (Gul et al. 2015). In general, the positive changes such as decreased bulk density and increased porosity, water holding capacity, pH, and nutrient pools, will also have positive effects on soil microbial abundance and activity (Lehmann et al. 2011; Gul et al. 2015). In addition, because of the specific characteristics of biochar including its high surface area, high porosity and abundance of pores of various sizes, biochar will provide a habitat for soil microorganisms, and will promote their growth (Fig. 1). The following sections are dedicated to the effects of biochar on soil microbial biomass and community structure.
5.1 Microbial biomass
The application of biochar has long been assumed to significantly influence soil MBC level. However, a consensus has not been reached regarding the effects of biochar on soil MBC (Gul et al. 2015). Biochar addition at various rates (0.45 and 2.27%, w/w) to a coarse textured soil decreased MBC after 10 weeks of a pot experiment (soil incubated between 13 and 25 °C, and at 50% of the soil’s water holding capacity) (Dempster et al. 2012). But in long-term field experiments, it was found that soil MBC concentrations either increased or did not change significantly after several years of regular biochar applications (Jones et al. 2012; Rousk et al. 2013; Zheng et al. 2016). A previous meta-analysis including different soil and land use types conducted by Biederman and Harpole (2013) suggested that biochar application resulted in a significant increase in soil MBC. Recently, another meta-analysis across soils under different land uses suggested that MBC content increased on average by 18% (12–23%) after biochar application across 395 paired observations (Liu et al. 2016).
However, changes in MBC were quite variable depending on biochar type and application rate, land use type, experimental method, soil texture, and fertilization management (Liu et al. 2016). Among these factors, application rate could be one of the most important drivers for the different responses of MBC to biochar application. Unlike in agricultural systems, where biochar application rates of biochar are usually larger than 10 t ha−1 and applications are frequent in order to increase plant productivity and crop yields, application rates in forest systems are generally much lower. Although the application of biochar to forest ecosystems has received less attention compared with agricultural systems, a few studies suggest that biochar amendment at a low rate did not change microbial biomass in forest soils (Noyce et al. 2015; Wang et al. 2014b). For example, Noyce et al. (2015) found that biochar application at a rate of 5 t ha−1 had no effect on soil MBC concentration in a tolerant hardwood forest after 1 or 2 years of biochar applications. Another study by Wang et al. (2014b) also showed that biochar application at a rate of 5 t ha−1 increased soil MBC concentration only in the first 2 months after application in a Chinese chestnut plantation soil. Domene et al. (2014) found that low application rates (1 and 3 t ha−1) of biochar did not result in changes of soil MBC concentrations, while the high application rate of 30 t ha−1 significantly increased soil MBC concentration. Similarly, Maestrini et al. (2014) found that the application of ryegrass-derived biochar increased microbial biomass at an application rate equivalent to 27 t ha−1 after a 158-day incubation period time (incubation at 27 °C and 70% of water holding capacity) in a Cambisol forest soil. All of the abovementioned results indicate that the effect of biochar application on soil MBC concentration are generally short-lived and rate-dependent.
The short-term effects of biochar application on enhancing MBC can be attributed to the release or dissolution of biological oil condensates formed during pyrolysis and present in biochar particles (Smith et al. 2010). These release and/or dissolution processes frequently occur in the first 2 months after biochar application. In addition, it is also possible that the porous structure of biochar material may potentially provide a suitable habitat for microorganism, such as providing labile available organic C and increasing water retention, acting as a refuge, and protecting microorganisms from predators (Lehmann et al. 2011; Luo et al. 2013; Quilliam et al. 2013; Chen et al. 2013, 2015). However, other studies argued that biochar amendment at relatively high rates may have a negative effect on soil MBC, as larger amounts of biochar with high C/N ratio tended to induce the immobilization of soil microbial N, reducing microbial activities (Ameloot et al. 2013). Nevertheless, more research is needed to investigate the reasons for such contradictory results and the mechanisms of how biochar affects MBC.
5.2 Microbial community structure
Soil microbial community structure is also assumed to be significantly affected by the application of biochar (Gul et al. 2015; Luo et al. 2017a). However, the effects of biochar on fungal and bacterial abundance and diversity patterns do not follow clear trends. Mitchell et al. (2015) reported that biochar application at 10 and 20 t ha−1 resulted in a significant increase of the bacterial/fungal ratio and a decreased Gram-negative/Gram-positive bacteria ratio in a temperate forest soil. In a 6-month laboratory incubation study, Santos et al. (2012) observed that biochar was utilized by all bacteria groups, especially Gram-positive bacteria, in temperate forest soils. Based on DNA sequencing technique, Khodadad et al. (2011) also found that application of oak and grass biochar significantly increased the abundance of several actinobacterial families (i.e., Gram-positive bacteria) in a Floridian forest soil. It is not surprising that Actinobacteria were stimulated by biochar applications as members in this group play a role in pyrogenic C metabolism and grow readily on carbon-rich refractory materials (O’Neill et al. 2009). These results indicate that biochar application may favor the growth of bacteria, in particular Gram-positive bacteria. Similar results have also been observed by Chen et al. (2013), who found that biochar amendments increased bacterial but decreased fungal gene abundance in a rice paddy soil.
The varied responses of bacterial and fungal communities to biochar applications might be closely related to their ecological characteristics and functioning, because bacteria and fungi differ strongly in their nutrient demand, turnover rate, and stress tolerance, for example, resilience to pH and water stress (Rousk et al. 2009). Compared with fungi, bacteria are more sensitive to labile substrate (Khodadad et al. 2011; Lehmann et al. 2011). Therefore, the labile C in biochar could be an important driver for bacterial growth directly after biochar applications (Ameloot et al. 2013; Farrell et al. 2013). Besides, the typical size of fungal hyphae is generally larger than bacteria, which may prohibit them from colonizing micropores. As a result, bacteria could be better protected from grazing than fungi, especially in smaller pores (Chen et al. 2013). Increase in soil pH may also play a key role in regulating microbial abundance and diversity, since neutral or slightly alkaline conditions are known to favor bacterial growth (Rousk et al. 2009).
A few researchers stated that biochar could also enhance fungal growth and activity, because fungi have the ability to colonize on carbon materials with low quality, such as char with a high proportion of aromatic C compound (Hockaday et al. 2007; Jin 2010; Lehmann et al. 2011; Li et al. 2017a). Supporting these statements, Mitchell et al. (2016) showed that fungal PLFA concentrations increased significantly 3 years after biochar was applied together with P fertilizer in a P-limited temperate hardwood forest in Ontario, Canada. Steinbeiss et al. (2009) showed that the application of biochar that was pyrolyzed from yeast promoted fungi and significantly decreased the bacterial/fungal ratio in both agricultural and forest soils, while glucose-derived biochar stimulated Gram-negative bacteria, suggesting that the responses of bacteria and fungi to biochar amendment vary and could depend on biochar feedstock. Moreover, our study (Chen et al. 2017) found that bamboo biochar increased fungal PLFA concentrations and the fungal/bacterial ratio, changed microbial community structure in a bamboo plantation soil, but such effects were largely dependent on the application rate and biochar particle size. Some wood-decaying fungal species can utilize biochar as a carbon substrate, thus enhancing their growth (Fontaine et al. 2011). The increased fungal/bacterial ratio may imply a change in microbial function towards decreased carbon loss because a fungal-dominated microbial community is believed to improve carbon use efficiency (Lehmann et al. 2011; Chen et al. 2013). Intriguingly, using the same study system as Mitchell et al. (2015), Noyce et al. (2015) found that biochar application at a rate of 5 t ha−1 had no significant effect on the bacterial and fungal community compositions or the fungal/bacterial ratio. The difference in results might be due to the application of biochar to the soil surface (0–20 cm) by Noyce et al. (2015), while the biochar was thoroughly mixed into the soil in the incubation study of Mitchell et al. (2015). These results highlight that the effect of biochar application on soil microbial community structure is complicated, especially since biochar applications significantly influence soil physical and chemical properties, which may then lead to complex interactions affecting soil microbial community characteristics (Gul et al. 2015).
6 Effects of biochar on soil greenhouse gas emissions
Soil carbon dioxide (CO2) emissions, also known as soil respiration, form the main pathway for soil organic carbon to enter the atmosphere. It is the primary mechanism of carbon loss from terrestrial ecosystems contributing to climate change (Peng et al. 2008; Xu and Shang 2016). Furthermore, methane (CH4) and nitrous oxide (N2O) are regarded as major greenhouse gases, and their global warming potential per unit mass are 25 and 198 times that of CO2, respectively, at the century scale (IPCC 2014). As outlined above, the incorporation of biochar into soil can change soil physical, chemical, and biological properties significantly, and consequently, it has also significant effects on the soil’s greenhouse emissions (Fig. 1). In the following sections, we consider how biochar application affects soil CO2, N2O and CH4 emissions, and discuss the mechanisms involved in the response of soil greenhouse gas emissions to biochar application.
6.1 Soil CO2 emission
Biochar addition significantly affects soil water content, porosity, pH, cation exchange capacity, carbon and nitrogen dynamics, and plant productivity, which all can have a significant effect on soil CO2 emissions (Jones et al. 2011; Stavi and Lal 2013; Luo et al. 2017b). However, the effect of biochar application on soil CO2 fluxes in forest ecosystems varies considerably among studies. The application of biochar to forest soils increased, decreased, or had negligible effects on CO2 emissions (Table 1). Mitchell et al. (2015) reported that the application of sugar maple biochar (5, 10, and 20 t ha−1) significantly increased soil CO2 emissions in a temperate forest soil. Johnson et al. (2017) also reported increased CO2 emissions from a biochar-amended soil compared to the emissions from the untreated control soil. This was corroborated by the findings of Hawthorne et al. (2017), who reported significantly higher CO2 fluxes from a Douglas-fir forest soil treated with 10% biochar compared to the emissions from the same soil treated with 1% biochar. The lowest CO2 flux was observed from the untreated control soil. In contrast, Sun et al. (2014) reported that the application of biochar (30 t ha−1) significantly reduced CO2 emissions by 31.5% from pine forest soils. Malghani et al. (2013) found in an incubation experiment that biochar application did not affect the CO2 emissions from a forest soil. Similarly, field studies conducted by Wang et al. (2014b), Sackett et al. (2015), and Zhou et al. (2017) also reported that biochar applications did not influence soil CO2 fluxes from forest soils. The variable effects of biochar application on soil CO2 flux in the above studies might be explained by differences in the type and rate of biochar, vegetation, and soil types, in addition to the time period between CO2 measurement and biochar application (Sohi et al. 2010; Ennis et al. 2012; Woolf and Lehmann 2012).
The mechanisms underlying the effects of biochar application on soil CO2 emissions can be generally encapsulated by four processes: (1) the biochar itself contains labile organic carbon which contributes to the labile organic carbon pool in soils after its application, thereby promoting soil CO2 emissions (Yoo and Kang 2012; Mukherjee and Lal 2013; Spokas 2013); (2) biochar has a large adsorption capacity that can affect soil surface CO2 emissions by adsorbing soil CO2 molecules (Kasozi et al. 2010; Liang et al. 2010); (3) biochar application to soil influences soil physical and chemical properties including water content, porosity, aggregation, pH, and CEC (Liang et al. 2010; Jones et al. 2011), which then indirectly affect CO2 emissions; and (4) biochar application can significantly affect the diversity and activities of microbial taxa that are involved in CO2 production(Liu et al. 2009; Liu et al. 2011; Zhang et al. 2012; Mitchell et al. 2015; Wang et al. 2016).
6.2 Soil CH4 emission
Biochar has been shown to reduce CH4 emissions from water-logged rice paddies (Liu et al. 2011) and to enhance CH4 uptake in aerobic soils (Karhu et al. 2011). The few published studies on the application of biochar to forest soils suggest that biochar reduces soil CH4 emissions. Yu et al. (2013) reported that the application of chicken manure biochar (10%, w/w) significantly increased CH4 uptake in forest soils. In a field study, Xiao (2016) also showed that, regardless of the application rate, biochar treatment significantly increased soil CH4 uptake in an intensively managed Chinese chestnut plantation.
There are two primary mechanisms underlying this observed increased soil CH4 uptake. First, biochar application generally increases soil pH which favors the growth of methanotrophy (Inubushi et al. 2005; Jeffery et al. 2016). Second, biochar application decreases soil bulk density and increases soil porosity, which favors CH4 oxidation and uptake activity by soil bacteria (Brassard et al. 2016). Increased soil aeration and porosity induced by biochar application and the consequent promotion of oxic conditions generally decrease CH4 production, because CH4 oxidation is an aerobic metabolic process, that is dependent on oxygen availability (Brassard et al. 2016).
Most studies have confirmed a reduction in CH4 emissions from biochar-amended soils, but a few studies have suggested that the application of biochar did not affect soil CH4 emissions (Malghani et al. 2013; Sackett et al. 2015; Lin et al. 2017), and in some cases, even reduced soil CH4 uptake (Hawthorne et al. 2017). Malghani et al. (2013) found that the addition of corn silage biochar (1%, w/w) had no significant effect on the CH4 emissions from a deciduous forest soil. A recent study also reported that there was no significant difference in CH4 flux between biochar-treated and control soils in a temperate hardwood forest (Sackett et al. 2015). Similarly, Lin et al. (2017) reported that either sawdust biochar application (24 t ha−1) or chicken manure biochar application (24 t ha−1) did not affect CH4 uptake in a subtropic acidic forest soil. In contrast, Hawthorne et al. (2017) showed that biochar application (1 or 10% additions, w/w) significantly decreased soil CH4 uptake, with net CH4 oxidation decreasing concomitantly with increasing biochar application rates. Therefore, the mechanisms underlying CH4 flux from soils after biochar application, and especially concerning microbial metabolism, require further investigation.
6.3 Soil N2O emission
Evidence concerning the potential for reduced N2O emissions as a result of biochar application in dryland soils has been confirmed in many farmland soils (He et al. 2016a, b). Though limited in number, investigations of N2O emissions after biochar application in forest environments have indicated significantly reduced N2O emissions (Malghani et al. 2013; Sun et al. 2014; Xiao et al. 2016b). Sun et al. (2014) found that the application of biochar (30 t ha−1) to a pine forest soil significantly decreased (25.5%) cumulative N2O emissions. Malghani et al. (2013) also reported that the application of corn silage biochar (1%, w/w) to deciduous forest soils significantly decreased the N2O emissions in a spruce forest soil. Likewise, Xiao et al. (2016b) showed that biochar application at a rate of 5 t ha−1 to a Chinese chestnut forest reduced annual average flux and annual cumulative total soil N2O emissions by 27.4 and 20.5% for, respectively, compared to the control.
There are two predominant mechanisms for these reductions. First, biochar application significantly enhances soil aeration and oxygen concentration in the soil profile, which in turn inhibits soil denitrification by microorganisms, which primarily occurs under sub-oxic conditions (Yanai et al. 2007; Van Zwieten et al. 2010b). Second, biochar application results in the adsorption of NH4 + and/or NO3 − to biochar particles, which then enhances plant growth, reduces NH3 volatilization, or immobilizes nitrogen compounds. These processes decrease the inorganic nitrogen pool available for nitrifiers or denitrifiers, which produce N2O as a metabolic byproduct (Singh et al. 2010; Van Zwieten et al. 2010b; Clough et al. 2013).
In contrast to the above results, positive or non-significant effects have also been reported in some studies. Hawthorne et al. (2017) found that the application of 10% biochar in a forest soil significantly increased N2O emissions, while no significant effect was observed after the application of 1% biochar. Sackett et al. (2015) found that the application of biochar (5 t ha−1) in a temperate hardwood forest did not change soil N2O emission. Thus, the effects of biochar addition on soil N2O emission processes are quite complicated, and the mechanisms involved require further investigation.
7 Prospects for biochar application to forest soils
The application of biochar in forest soils has a number of benefits, including increased soil pH, CEC content, aggregate stability, and organic carbon stock, while reducing soil bulk density and soil greenhouse gas emissions. Such effects are biochar-, soil-, and plant-specific and can vary considerably among systems. In addition, the application of biochar is also regarded as an important practice for remediating soils contaminated with heavy metals and organic compounds (Zhang et al. 2013). Therefore, the application of biochar in forest soils can have considerable benefits. This is especially true for plantation soils with low organic carbon contents and slight to moderate levels of contamination (Thomas and Gale 2015). However, some issues still remain unsolved and the mechanisms by which biochar application affect soil processes are yet unclear and require further investigation. Below, we outline five specific recommendations to guide future investigations about the effects of biochar applications to forest soils.
-
1.
Recent studies have demonstrated that biochar application can significantly affect microbial community structure and diversity in forest soils. However, little information is available regarding the effect of biochar application on specific functions that are conducted by soil microorganisms and their gene functions that are related to carbon cycling (e.g., cbbL, cbhI, cel5, and lcc) and nitrogen cycling (e.g., nirK, nirS, nosZ, and narG), when compared to those of agricultural soils. Assessing the effects of biochar addition on the aforementioned microbial functions will help us better understand the mechanisms by which biochar affects the biogeochemical processing of soil nutrients in forest ecosystems.
-
2.
The impact of biochar addition on soil respiration components (i.e., autotrophic respiration and heterotrophic respiration) is still poorly understood, although overall respiration rates in forest ecosystems are well-studied (Wang et al. 2014b; Mitchell et al. 2015). Estimating the net primary productivity (NPP) and net ecosystem productivity (NEP) of forest ecosystems requires quantification of autotrophic respiration and heterotrophic respiration (Gower et al. 2001). Therefore, it is necessary to separately quantify soil respiration components during the assessment of biochar application effects on forest ecosystem soil carbon cycling.
-
3.
Biochar can have considerable advantages for improving soil physical, chemical, and biological properties. However, biochar application alone is not sufficient to meet the nutrient needs for tree growth and productivity. Thus, the study of new fertilizers (e.g., those rich in biochar and a mixture of certain nutrients) may be an effective way to mitigate depletion of soil organic carbon pools and the large nutrient requirements that are typical of intensively managed plantations.
-
4.
The application of biochar can directly affect tree growth, but it can also indirectly affect tree growth by modifying soil properties. Significant genotypic responses may differ among tree species related to types and rates of biochar applications. Thus, it is critical to conduct studies on the effects of different types of biochar on the growth of different tree species.
-
5.
Most of the studies regarding the effects of biochar application on soil properties were conducted through short-term incubation experiments that lasted mostly less than 3 years (Nguyen et al. 2017). The carbon in biochar is primarily composed of aromatic carbon molecules with soil residence times that can exceed 10 or even 100 years. Therefore, it is also critical to examine the long-term effects of biochar addition on soil properties and greenhouse gas emissions, which is of great significance for the effective application of biochar in forest soils.
-
6.
Assessing costs and benefits of biochar applications is complicated. Considering only the nutrient value of biochar, the costs of biochar applications exceed those of fertilizer applications. But as outlined in this review, biochar applications have many additional benefits including the improvement of soil properties and the mitigation of greenhouse gas emissions. In contrast, long-term chemical fertilization has negative effects on soil properties and carbon sequestration. However, as far as we know, no cost-benefit analysis for biochar application in forest ecosystems has been conducted yet. Prior to promoting field-scale applications of biochar in forest ecosystems, a comprehensive cost-benefit analysis of biochar application in forest ecosystems is required.
-
7.
Although most case studies have reported positive effects of biochar on soil properties in forest ecosystems, there might be some so far less studied adverse effects of biochar on forest soils. Recently, it has been reported that during the production of biochar, other materials, such as polycyclic aromatic hydrocarbons (PAHs) and volatile organic compounds (VOCs), were produced and remained on the surface of biochar particles (Dutta et al. 2017). Such types of materials would negatively affect the soil microbial community and the growth of tree plants (Dutta et al. 2017). Therefore, the ecotoxicological effects of biochar application on the growth of soil microorganisms and tree plants in forest ecosystems need to be investigated in future study.
References
Abel S, Peters A, Trinks S, Schonsky H, Facklam M, Wessolek G (2013) Impact of biochar and hydrochar addition on water retention and water repellency of sandy soil. Geoderma 202–203:183–191
Ahmad M, Lee SS, Lim JE, Lee SE, Cho JS, Moon DH, Hashimoto Y, Ok YS (2014) Speciation and phytoavailability of lead and antimony in a small arms range soil amended with mussel shell, cow bone and biochar: EXAFS spectroscopy and chemical extractions. Chemosphere 95:433–441
Alameda D, Villar R, Iriondo JM (2012) Spatial pattern of soil compaction: trees’ footprint on soil physical properties. For Ecol Manag 283:128–137
Ameloot N, De Neve S, Jegajeevagan K, Yildiz G, Buchan D, Funkuin YN, Prins W, Bouckaert L, Sleutel S (2013) Short-term CO2 and N2O emissions and microbial properties of biochar amended sandy loam soils. Soil Biol Biochem 57:401–410
Angın D, Altintig E, Köse TE (2013) Influence of process parameters on the surface and chemical properties of activated carbon obtained from biochar by chemical activation. Bioresour Technol 148:542–549
Artiola JF, Rasmussen C, Freitas R (2012) Effects of a biochar-amended alkaline soil on the growth of romaine lettuce and bermudagrass. Soil Sci 177:561–570
Atkinson CJ, Fitzgerald JD, Hipps NA (2010) Potential mechanisms for achieving agricultural benefits from biochar application to temperate soils: a review. Plant Soil 337:1–18
Bai SH, Xu Z, Blumfield TJ, Reverchon F (2015) Human footprints in urban forests: implication of nitrogen deposition for nitrogen and carbon storage. J Soils Sediments 15:1927–1936
Basso AS, Miguez FE, Laird DA, Horton R, Westgate M (2013) Assessing potential of biochar for increasing water-holding capacity of sandy soils. GCB Bioenergy 5:132–143
Biederman LA, Harpole WS (2013) Biochar and its effects on plant productivity and nutrient cycling: a meta -analysis. GCB Bioenergy 5:202–214
Bossuyt H, Denef K, Six J, Frey SD, Merckx R, Paustian K (2001) Influence of microbial populations and residue quality on aggregate stability. Appl Soil Ecol 16:195–208
Brassard P, Godbout S, Raghavan V (2016) Soil biochar amendment as a climate change mitigation tool: Key parameters and mechanisms involved. J Environ Manag 181:484–497
Brewer CE, Schmidt-Rohr K, Satrio JA, Brown RC (2009) Characterization of biochar from fast pyrolysis and gasification systems. Environ Prog Sustain 28:386–396
Bruun EW, Petersen CT, Hansen E, Holm JK, Hauggaard-nielsen H (2014) Biochar amendment to coarse sandy subsoil improves root growth and increases water retention. Soil Use Manag 30:109–118
Brzostek ER, Dragoni D, Schmid HP, Rahman AF, Sims D, Wayson CA, Johnson DJ, Phillips RP (2014) Chronic water stress reduces tree growth and the carbon sink of deciduous hardwood forests. Glob Chang Biol 20:2531–2539
Burrell LD, Zehetner F, Rampazzo N, Wimmer B, Soja G (2016) Long-term effects of biochar on soil physical properties. Geoderma 282:96–102
Busscher WJ, Novak JM, Evans DE, Watts DW, Niandou MAS, Ahmedna M (2010) Influence of pecan biochar on physical properties of a norfolk loamy sand. Soil Sci 175:10–14
Busscher WJ, Novak JM, Ahmedna M (2011) Physical effects of organic matter amendment of a southeastern US coastal loamy sand. Soil Sci 176:661–667
Bussotti F, Pollastrini M, Holland V, Brüggemann W (2015) Functional traits and adaptive capacity of European forests to climate change. Environ Exp Bot 111:91–113
Cameron KC, Buchan GD (2006) Porosity and pore size distribution. In: Lal R (ed) Encyclopedia of soil science. CRC Press, Boca Raton, pp 1350–1353
Cardoso EJBN, Vasconcellos RLF, Bini D, Miyauchi MYH, Santos CAD, Alves PRL, Paula AMD, Nakatani AS, Pereira JDM, Nogueira MA (2013) Soil health: looking for suitable indicators What should be considered to assess the effects of use and management on soil health? Sci Agric 70:274–289
Castellini M, Giglio L, Niedda M, Palumbo AD, Ventrella D (2015) Impact of biochar addition on the physical and hydraulic properties of a clay soil. Soil Tillage Res 154:1–13
Chang L, Wang BF, Liu XH, Callaham MA, Ge F (2017) Recovery of collembola in pinus tabulaeformis plantations. Pedosphere 27:129–137
Chen J, Liu X, Zheng J, Zhang B, Lu H, Chi Z, Pan G, Li L, Zheng J, Zhang X, Wang J, Yu X (2013) Biochar soil amendment increased bacterial but decreased fungal gene abundance with shifts in community structure in a slightly acid rice paddy from Southwest China. Appl Soil Ecol 71:33–44
Chen J, Liu X, Li L, Zheng J, Qu J, Zheng J, Zhang X, Pan G (2015) Consistent increase in abundance and diversity but variable change in community composition of bacteria in topsoil of rice paddy under short term biochar treatment across three sites from South China. Appl Soil Ecol 91:68–79
Chen JH, Li SH, Liang CF, Xu QF, Li YC, Qin H, Fuhrmann JJ (2017) Response of microbial community structure and function to short-term biochar amendment in an intensively managed bamboo (Phyllostachys praecox) plantation soil: effect of particle size and addition rate. Sci Total Environ 574:24–33
Cheng CH, Lehmann J, Engelhard MH (2008) Natural oxidation of black carbon in soils: changes in molecular form and surface charge along a climosequence. Geochim Cosmochim Acta 72:1598–1610
Clough TJ, Condron LM, Kammann C, Müller C (2013) A review of biochar and soil nitrogen dynamics. Agronomy 3:275–293
Dai ZM, Zhang XJ, Tang C, Muhammad N, Wu JJ, Brookes PC, Xu JM (2017) Potential role of biochars in decreasing soil acidification—a critical review. Sci Total Environ 581–582:601–611
Dempster D, Gleeson D, Solaiman Z, Jones D, Murphy D (2012) Decreased soil microbial biomass and nitrogen mineralisation with Eucalyptus biochar addition to a coarse textured soil. Plant Soil 354:311–324
Deng W, Van Zwieten L, Lin Z, Liu X, Sarmah AK, Wang H (2017) Sugarcane bagasse biochars impact respiration and greenhouse gas emissions from a latosol. J Soils Sediments 17:632–640
Ding Y, Liu YG, Liu SB, Li ZW, Tan XF, Huang XX, Zheng GM, Zhou L, Zheng BH (2016) Biochar to improve soil fertility: a review. Agron Sustain Dev 36:36
Domene X, Mattana S, Hanley K, Enders A, Lehmann J (2014) Mediumterm effects of corn biochar addition on soil biota activities and functions in a temperate soil cropped to corn. Soil Biol Biochem 72:152–162
Dong D, Yang M, Wang C, Wang H, Li Y, Luo J, Wu W (2013) Responses of methane emissions and rice yield to applications of biochar and straw in a paddy field. J Soils Sediments 13:1450–1460
Dong D, Feng Q, McGrouther K, Yang M, Wang H, Wu W (2015) Effects of biochar amendment on rice growth and nitrogen retention in a waterlogged paddy field. J Soils Sediments 15:153–162
Durenkamp M, Luo Y, Brookes PC (2010) Impact of black carbon addition to soil on the determination of soil microbial biomass by fumigation extraction. Soil Biol Biochem 42:2026–2029
Dutta T, Kwon E, Bhattacharya SS, Jeon BH, Deep A, Uchimiya M, Kim KH (2017) Polycyclic aromatic hydrocarbons and volatile organic compounds in biochar and biochar-amended soil: a review. GCB Bioenergy 9:990–1004
Ennis CJ, Evans AG, Islam M, Ralebitso-Senior TK, Senior E (2012) Biochar: carbon sequestration, land remediation, and impacts on soil microbiology. Crit Rev. Environ Sci Technol 42:2311–2364
Fang JY, Chen AP, Peng CH, Zhao SQ, Ci LJ (2001) Changes in forest biomass carbon storage in China between 1949 and 1998. Science 292:2320–2322
Fargeon H, Aubry-Kientz M, Brunaux O, Descroix L, Gaspard R, Guitet S, Rossi V, Hérault B (2016) Vulnerability of commercial tree species to water stress in logged forests of the guiana shield. Forests 7:1–21
Farrell M, Kuhn TK, Macdonald LM, Maddern TM, Murphy DV, Hall PA, Singh BP, Baumann K, Krull ES, Baldock JA (2013) Microbial utilisation of biochar-derived carbon. Sci Total Environ 465:288–297
Fontaine S, Henault C, Aamor A, Bdioui N, Bloor J, Maire V, Mary B, Revaillot S, Maron P (2011) Fungi mediate long term sequestration of carbon and nitrogen in soil through their priming effect. Soil Biol Biochem 43:86–96
Gaskin JW, Steiner C, Harris K, Das KC, Bibens B (2008) Effect of low-temperature pyrolysis conditions on biochar for agricultural use. Trans Asabe 51:2061–2069
Gaskin JW, Speir RA, Harris K, Das KC, Lee RD, Morris LA, Fisher DS (2010) Effect of peanut hull and pine chip biochar on soil nutrients, corn nutrient status, and yield. Agron J 102:623–633
Glaser B, Lehmann J, Zech W (2002) Ameliorating physical and chemical properties of highly weathered soils in the tropics with charcoal—a review. Biol Fertil Soils 35:219–230
Glisczynski FV, Pude R, Amelung W, Sandhage-Hofmann A (2016) Biochar-compost substrates in short-rotation coppice: effects on soil and trees in a three-year field experiment. J Plant Nutr Soil Sci 179:574–583
Gower ST, Krankina O, Olson RJ, Apps M, Linder S, Wang C (2001) Net primary production and carbon allocation patterns of boreal forest ecosystems. Ecol Appl 11:1395–1411
Gul S, Whalen JK, Thomas BW, Sachdeva V, Deng H (2015) Physico-chemical properties and microbial responses in biochar-amended soils: mechanisms and future directions. Agric Ecosyst Environ 206:46–59
Gundale MJ, Nilsson MC, Pluchon N, Wardle DA (2016) The effect of biochar management on soil and plant community properties in a boreal forest. GCB Bioenergy 8:777–789
Hamer U, Marschner B, Brodowski S, Amelung W (2004) Interactive priming of black carbon and glucose mineralization. Org Geochem 35:823–830
Hartmann M, Niklaus PA, Zimmermann S, Schmutz S, Kremer J, Abarenkov K, Lüscher P, Widmer F, Frey B (2014) Resistance and resilience of the forest soil microbiome to logging-associated compaction. ISME J 8:226
Hawthorne I, Johnson MS, Jassal RS, Black TA, Grant NJ, Smukler SM (2017) Application of biochar and nitrogen influences fluxes of CO2, CH4 and N2O in a forest soil. J Environ Manag 192:203–214
He L, Gielen G, Bolan N, Zhang X, Qin H, Huang H, Wang H (2015) Contamination and remediation of phthalic acid esters in agricultural soils in China: a review. Agron Sustain Dev 35:519–534
He L, Fan S, Müller K, Hu G, Huang H, Zhang X, Lin X, Che L, Wang H (2016a) Biochar reduces the bioavailability of di-(2-ethylhexyl) phthalate in soil. Chemosphere 142:24–27
He YH, Zhou XH, Jiang LL, Li M, Du ZG, Zhou GY, Shao JJ, Wang XH, Xu ZH, Bai SH, Wallace H, Xu CY (2016b) Effects of biochar application on soil greenhouse gas fluxes: a meta-analysis. GCB Bioenergy 9:743–755
Hedwall PO, Gong P, Ingerslev M, Bergh J (2014) Fertilization in northern forests-biological, economic and environmental constraints and possibilities Scandinavian. J Forest Res-Jpn 29:301–311
Herath HMSK, Camps-Arbestain M, Hedley M (2013) Effect of biochar on soil physical properties in two contrasting soils: an Alfisol and an Andisol. Geoderma 209:188–197
Heydari M, Prévosto B, Naji HR, Mehrabi AA, Pothier D (2017) Influence of soil properties and burial depth on Persian oak (Quercus brantii, Lindl) establishment in different microhabitats resulting from traditional forest practices. Eur J Forest Res 136:1–19
Hockaday WC, Grannas AM, Kim S, Hatcher PG (2007) The transformation and mobility of charcoal in a fire-impacted watershed. Geochim Cosmochim Acta 71:3432e3445
Hseu ZY, Jien SH, Chien WH, Liou RC (2014) Impacts of biochar on physical properties and erosion potential of a mudstone slopeland soil. Sci World J. https://doi.org/10.1155/2014/602197
Hua L, Jin SS, Tang ZG (2012) Effect of bio-charcoal on release of carbon dioxide in soil. Anhui Agric Sci 40:6501–6503 (in Chinese)
Huang P, Ge C, Feng D, Yu H, Luo J, Li J, Strong PJ, Sarmah AK, Bolan NS, Wang H (2018) Effects of metal ions and pH on ofloxacin sorption to cassava residue-derived biochar. Sci Total Environ. https://doi.org/10.1016/j.scitotenv.2017.10.177
Ibrahim HM, Al-Wabel MI, Usman ARA, Al-Omran A (2013) Effect of Conocarpus biochar application on the hydraulic properties of a sandy loam soil. Soil Sci 178:165–173
Intergovernmental Panel on Climate Change (2014) Climate change 2014—impacts, adaptation and vulnerability: regional aspects. Cambridge University Press, Cambridge
Inubushi K, Otake S, Furukawa Y, Shibasaki N, Ali M, Itang AM, Tsuruta H (2005) Factors influencing methane emission from peat soils: comparison of tropical and temperate wetlands. Nutr Cycl Agroecosyst 71:93–99
Ito K, Uchiyama Y, Kurokami N, Sugano K, Nakanishi Y (2011) Soil acidification and decline of trees in forests within the precincts of shrines in Kyoto (Japan). Water Air Soil Pollut 214:197–204
Jeffery S, Verheijen F, Van Der Velde M, Bastos AC (2011) A quantitative review of the effects of biochar application to soils on crop productivity using meta-analysis. Agric Ecosyst Environ 144:175–187
Jeffery S, Verheijen FG, Kammann C, Abalos D (2016) Biochar effects on methane emissions from soils: a meta-analysis. Soil Biol Biochem 101:251–258
Jin H (2010) Characterization of microbial life colonizing biochar and biochar-amended soils. PhD Dissertation, Cornell University, Ithaca, NY
Johnson MS, Webster C, Jassal RS, Hawthorne I, Black TA (2017) Biochar influences on soil CO2 and CH4 fluxes in response to wetting and drying cycles for a forest soil. Sci Rep 7:6780
Jones DL, Murphy DV, Khalid M, Ahmad W, Edwards-Jones G, DeLuca TH (2011) Short-term biochar-induced increase in soil CO2 release is both biotically and abiotically mediated. Soil Biol Biochem 43:1723–1731
Jones DL, Rousk J, Edwards-Jones G, DeLuca TH, Murphy DV (2012) Biochar-mediated changes in soil quality and plant growth in a three year field trial. Soil Biol Biochem 45:113–124
Jorge RF, Almeida CXD, Borges EN, Passos RR (2012) Pore size distribution and soil bulk density in oxisols submitted to different management systems and use. Biosci J 28:159–169
Karhu K, Mattila T, Bergström I, Regina K (2011) Biochar addition to agricultural soil increased CH 4 uptake and water holding capacity-results from a short-term pilot field study. Agric Ecosyst Environ 140:309–313
Kasozi GN, Zimmerman AR, Nkedi-kizza P, Gao B (2010) Catechol and humic acid sorption onto a range of laboratory-produced black carbons (biochars). Environ Sci Technol 44:6189–6195
Khademalrasoul A, Naveed M, Heckrath G, Kumari KGID, Jonge LWD, Elsgaard L, Vogel HJ, Iversen BV (2014) Biochar effects on soil aggregate properties under no-till maize. Soil Sci 179:273–283
Khodadad CLM, Zimmerman AR, Green SJ, Uthandi S, Foster JS (2011) Taxa-specific changes in soil microbial community composition induced by pyrogenic carbon amendments. Soil Biol Biochem 43:385–392
Kleibl M, Klvač R, Lombardini C, Porhaly J, Spinelli R (2014) Soil compaction and recovery after mechanized final felling of Italian coastal pine plantations. Croat J For Eng 35:63–71
Kloss S, Zehetner F, Dellantonio A, Hamid R, Ottner F, Liedtke V, Schwanninger M, Gerzabek MH, Soja G (2012) Characterization of slow pyrolysis biochars: effects of feedstocks and pyrolysis temperature on biochar properties. J Environ Qual 41:990–1000
Kloss S, Zehetner F, Oburger E, Buecker J, Kitzler B, Wenzel WW, Wimmer B, Soja G (2014) Trace element concentrations in leachates and mustard plant tissue (Sinapis alba L.) after biochar application to temperate soils. Sci Total Environ 481:498–508
Kormanek M, Głąb T, Banach J, Szewczyk G (2015) Effects of soil bulk density on sessile oak Quercus petraea, Liebl seedlings. Eur J Forest Res 134:969–979
Kuzyakov Y, Subbotina I, Chen HQ, Bogomolova I, Xu XL (2009) Black carbon decomposition and incorporation into soil microbial biomass estimated by 14C labeling. Soil Biol Biochem 41:210–219
Laird DA, Fleming P, Davis DD, Horton R, Wang BQ, Karlen DL (2010) Impact of biochar amendments on the quality of a typical Midwestern agricultural soil. Geoderma 158:443–449
Lapenis AG, Lawrence GB, Andreev AA, Bobrov AA, Torn MS, Harden JW (2004) Acidification of forest soil in russia: from 1893 to present. Global Biogeochem Cycles 18:609–615
Lee JW, Kidder M, Evans BR, Paik S, Buchanan AC III, Garten CT, Brown RC (2010) Characterization of biochars produced from cornstovers for soil amendment. Environ Sci Technol 44:7970–7974
Lehmann J (2007) A handful of carbon. Nature 447:143–144
Lehmann J, da Silva JP, Steiner C, Nehls T, Zech W, Glaser B (2003) Nutrient availability and leaching in an archaeological Anthrosol and a Ferralsol of the Central Amazon basin: fertilizer, manure and charcoal amendments. Plant Soil 249:343–357
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
Lei OY, Zhang RD (2013) Effects of biochars derived from different feedstocks and pyrolysis temperatures on soil physical and hydraulic properties. J Soils Sediments 13:1561–1572
Lewis SA, Wu JQ, Robichaud PR (2006) Assessing burn severity and comparing soil water repellency, Hayman Fire, Colorado. Hydrol Process 20:1–16
Li YF, Zhang JJ, Chang SX, Jiang PK, Zhou GM, Fu SL, Yan ER, Wu JS, Lin L (2013) Long-term intensive management effects on soil organic carbon pools and chemical composition in Moso bamboo (Phyllostachys pubescens) forests in subtropical China. Forest Ecol Manag 303:121–130
Li YF, Zhang JJ, Chang SX, Jiang PK, Zhou GM, Shen ZM, Wu JS, Lin L, Wang ZS, Shen MC (2014) Converting native shrub forests to Chinese chestnut plantations and subsequent intensive management affected soil C and N pools. For Ecol Manag 312:161–169
Li YC, Li YF, Chang SX, Liang X, Qin H, Chen JH, Xu QF (2017a) Linking soil fungal community structure and function to soil organic carbon chemical composition in intensively managed subtropical bamboo forests. Soil Biol Biochem 107:19–31
Li ZG, Gu CM, Zhang RH, Ibrahim M, Zhang GS, Wang L, Zhang RQ, Chen F, Liu Y (2017b) The benefic effect induced by biochar on soil erosion and nutrient loss of slopping land under natural rainfall conditions in central China. Agric Water Manag 185:145–150
Liang B, Lehmann J, Solomon D, Kinyangi J, Grossman J, O’Neill B, Skjemstad JO, Thies J, Luizão FJ, Petersen J, Neves EG (2006) Black carbon increases cation exchange capacity in soil. Soil Sci Soc Am J 70:1719–1730
Liang BQ, Lehmann J, Sohi SP, Thies JE, O’Neill B, Trujillo L, Gaunt J, Solomon D, Grossman J, Neves EG, Luizãoc FJ (2010) Black carbon affects the cycling of non-black carbon in soil. Org Geochem 41:206–213
Lin ZB, Liu Q, Liu G, Cowie AL, Bei QC, Liu BJ, Wang XJ, Ma J, Zhu JG, Xie ZB (2017) Effects of different biochars on Pinus elliottii growth, N use efficiency, soil N2O and CH4 emissions and C storage in a subtropical area of China. Pedosphere 27:248–261
Liu QS, Liu Y, Show KY, Tay JH (2009) Toxicity effect of phenol on aerobic granules. Environ Technol 30:69–74
Liu YX, Yang M, Wu YM, Wang HL, Chen YX, Wu WX (2011) Reducing CH4 and CO2 emissions from waterlogged paddy soil with biochar. J Soils Sediments 11:930–939
Liu XY, Li LQ, Bian RJ, Chen D, Qu JJ, Wanjiru Kibue G, Pan GX, Zhang XH, Zheng JW, Zheng JF (2014) Effect of biochar amendment on soil-silicon availability and rice uptake. J Plant Nutr Soil Sci 177:91–96
Liu S, Zhang Y, Zong Y, Hu Z, Wu S, Zhou J, Jin Y, Zou J (2016) Response of soil carbon dioxide fluxes, soil organic carbon and microbial biomass carbon to biochar amendment: a meta-analysis. GCB Bioenergy 8:392–406
Lorenz K, Lal R (2014) Biochar application to soil for climate change mitigation by soil organic carbon sequestration. J Plant Nutr Soil Sci 177:651–670
Lu K, Yang X, Shen J, Robinson B, Huang H, Liu D, Bolan N, Pei J, Wang H (2014a) Effect of bamboo and rice straw biochars on the bioavailability of Cd, Cu, Pb and Zn to Sedum plumbizincicola. Agric Ecosyst Environ 191:124–132
Lu SG, Sun FF, Zong YT (2014b) Effect of rice husk biochar and coal fly ash on some physical properties of expansive clayey soil (Vertisol). Catena 114:37–44
Lu K, Yang X, Gielen G, Bolan N, Ok YS, Niazi NK, Xu S, Yuan G, Chen X, Zhang X, Liu D, Song Z, Liu X, Wang H (2017) Effect of bamboo and rice straw biochars on the mobility and redistribution of heavy metals (Cd, Cu, Pb and Zn) in contaminated soil. J Environ Manage 186(Part 2):285–292
Luo Y, Durenkamp M, Lin QM, Nobili M, Brookes PC (2011) Soil priming effects and the mineralisation of biochar following its incorporation to soils of different pH. Soil Biol Biochem 43:2304–2314
Luo Y, Durenkamp M, Lin QM, Nobili M, Devonshire BJ, Brookes PC (2013) Microbial biomass growth, following incorporation of biochars produced at 350°C or 700°C, in a silty-clay loam soil of high and low pH. Soil Biol Biochem 57:513–523
Luo Y, Yu ZY, Zhang KL, Xu JM, Brookes PC (2016) The properties and functions of biochars in forest ecosystems. J Soils Sediments 16:2005–2020
Luo Y, Lin Q, Durenkamp M, Dungait AJ, Brookes PC (2017a) Soil priming effects following substrates addition to biochar-treated soils after 431 days of pre-incubation. Biol Fertil Soils 53:315–326
Luo Y, Zang HD, Yu ZY, Chen ZY, Gunina A, Kuzyakov Y, Xu JM, Zhang KL, Brookes PC (2017b) Priming effects in biochar enriched soils using a three-source-partitioning approach: 14C labelling and 13C natural abundance. Soil Biol Biochem 106:28–35
Maestrini B, Herrmann AM, Nannipieri P, Schmidt MWI, Abiven S (2014) Ryegrass-derived pyrogenic organic matter changes organic carbon and nitrogen mineralization in a temperate forest soil. Soil Biol Biochem 69:291–301
Malghani S, Gleixner G, Trumbore SE (2013) Chars produced by slow pyrolysis and hydrothermal carbonization vary in carbon sequestration potential and greenhouse gases emissions. Soil Biol Biochem 62:137–146
Manyà JJ (2012) Pyrolysis for biochar purposes: a review to establish current knowledge gaps and research needs. Environ Sci Technol 46:7939–7954
Mao JD, Johnson RL, Lehmann J, Olk DC, Neves EG, Thompson ML, Schmidt-Rohr K (2012) Abundant and stable char residues in soils: implications for soil fertility and carbon sequestration. Environ Sci Technol 46:9571–9576
Mertens J, Germer J, de Araújo Filho JC, Sauerborn J (2017) Effect of biochar, clay substrate and manure application on water availability and tree-seedling performance in a sandy soil. Arch Agron Soil Sci 63:969–983
Mitchell PJ, Simpson AJ, Soong R, Simpson MJ (2015) Shifts in microbial community and water-extractable organic matter composition with biochar amendment in a temperate forest soil. Soil Biol Biochem 81:244–254
Mitchell PJ, Simpson AJ, Soong R, Schurman JS, Thomas SC, Simpson MJ (2016) Biochar amendment and phosphorus fertilization altered forest soil microbial community and native soil organic matter molecular composition. Biogeochemistry 130:227–245
Moyano FE, Manzoni S, Chenu C (2013) Responses of soil heterotrophic respiration to moisture availability: an exploration of processes and models. Soil Biol Biochem 59:72–85
Mukherjee A, Lal R (2013) Biochar impacts on soil physical properties and greenhouse gas emissions. Agronomy 3:313–339
Mukherjee A, Zimmerman AR, Harris W (2011) Surface chemistry variations among a series of laboratory-produced biochars. Geoderma 163:247–255
Nawaz MF, Bourrié G, Trolard F (2013) Soil compaction impact and modelling a review. Agron Sustain Dev 33:291–309
Nguyen BT, Lehmann J, Hockaday WC, Joseph S, Masiello CA (2010) Temperature sensitivity of black carbon decomposition and oxidation. Environ Sci Technol 44:3324–3331
Nguyen TT, Xu CY, Tahmasbian I, Che RX, Xu ZH, Zhou XH, Wallace HM, Bai SH (2017) Effects of biochar on soil available inorganic nitrogen: a review and meta-analysis. Geoderma 288:79–96
Niazi NK, Bibi I, Shahid M, Ok YS, Burton ED, Wang H, Shaheen SM, Rinklebe J, Lüttge A (2018) Arsenic removal by perilla leaf biochar in aqueous solutions and groundwater: an integrated spectroscopic and microscopic examination. Environ Pollut 232:31–41
Novak JM, Lima I, Xing B, Gaskin JW, Steiner C, Das KC, Ahmedna M, Rehrah D, Watts DW, Busscher WJ, Schomberg H (2009) Characterization of designer biochar produced at different temperatures and their effects on a loamy sand. Ann Environ Sci 3:195–206
Noyce GL, Basiliko N, Fulthorpe R, Sackett TE, Thomas SC (2015) Soil microbial responses over 2 years following biochar addition to a north temperate forest. Biol Fertil Soils 51:649–659
O’Neill B, Grossman J, Tsai M, Gomes J, Lehmann J, Peterson J, Neves E, Thies J (2009) Bacterial community composition in Brazilian Anthrosols and adjacent soils characterized using culturing and molecular identification. Microb Ecol 58:23–35
Obia A, Mulder J, Martinsen V, Cornelissen G, Børresen T (2016) In situ effects of biochar on aggregation, water retention and porosity in light-textured tropical soils. Soil Tillage Res 155:35–44
Ohlson M, Dahlberg B, Økland T, Brown KJ, Halvorsen R (2009) The charcoal carbon pool in boreal forest soils. Nat Geosci 2:692–695
Ouyang L, Wang F, Tang J, Yu L, Zhang R (2013) Effects of biochar amendment on soil aggregates and hydraulic properties. J Soil Sci Plant Nutr 13:991–1002
Page-Dumroese DS, Coleman M, Thomas SC (2015) Opportunities and uses of biochar on forest sites in North America. In: Bruckman VJ, Varol EA, Uzun BB, Liu J (eds) Biochar: a regional supply chain approach in view of mitigating climate change. Cambridge University Press, Cambridge
Payn T, Carnus JM, Freer-Smith P, Kimberley M, Kollert W, Liu S, Wingfield MJ (2015) Changes in planted forests and future global implications. Forest Ecol Manag 352:57–67
Peng YY, Thomas SC, Tian DL (2008) Forest management and soil respiration: implications for carbon sequestration. Environ Rev 16:93–111
Peng X, Ye LL, Wang CH, Zhou H, Sun B (2011) Temperature- and duration-dependent rice straw-derived biochar: characteristics and its effects on soil properties of an ultisol in southern China. Soil Tillage Res 112:159–166
Prayogo C, Jones JE, Baeyens J, Bending GD (2014) Impact of biochar on mineralisation of C and N from soil and willow litter and its relationship with microbial community biomass and structure. Biol Fertil Soils 50:695–702
Prober SM, Stol J, Piper M, Gupta VVSR, Cunningham SA (2014) Enhancing soil biophysical condition for climate-resilient restoration in mesic woodlands. Ecol Eng 71:246–255
Qi F, Kuppusamy S, Naidu R, Bolan NS, Ok YS, Lamb D, Li Y, Yu L, Semple KT, Wang H (2017) Pyrogenic carbon and its role in contaminant immobilization in soils. Crit Rev Environ Sci Technol. https://doi.org/10.1080/10643389.2017.1328918
Quilliam RS, Glanville HC, Wade SC, Jones DL (2013) Life in the ‘charosphere’—does biochar in agricultural soil provide a significant habitat for microorganisms? Soil Biol Biochem 65:287–293
Rhoades CC, Minatre KL, Pierson DN, Fegel TS, Cotrufo MF, Kelly EF (2017) Examining the potential of forest residue-based amendments for post-wildfire rehabilitation in Colorado, USA. Scientifica. https://doi.org/10.1155/2017/4758316
Rousk J, Brookes PC, Bååth E (2009) Contrasting soil pH effects on fungal and bacterial growth suggest functional redundancy in carbon mineralization. Appl Environ Microbiol 75:1589–1596
Rousk J, Dempster DN, Jones DL (2013) Transient biochar effects on decomposer microbial growth rates: evidence from two agricultural case-studies. Eur J Soil Sci 64:770–776
Sackett TE, Basiliko N, Noyce GL, Winsborough C, Schurman J, Ikeda C, Thomas SC (2015) Soil and greenhouse gas responses to biochar additions in a temperate hardwood forest. GCB Bioenergy 7:1062–1074
Sankura H, Lemma B, Ram N (2014) Effect of changing natural forest and wetland to other land uses on soil properties and stocks of carbon and nitrogen in south Ethiopia. Carpath J Earth Env 9:259–265
Santin C, Doerr SH, Preston CM, Gonzalez-Rodriguez G (2015) Pyrogenic organic matter production from wildfires: a missing sink in the global carbon cycle. Glob Chang Biol 21:1621–1633
Santos F, Torn MS, Bird JA (2012) Biological degradation of pyrogenic organic matter in temperate forest soils. Soil Biol Biochem 51:115–124
Scheer C, Grace PR, Rowlings DW, Kimber S, Van Zwieten L (2011) Effect of biochar amendment on the soil-atmosphere exchange of greenhouse gases from an intensive subtropical pasture in northern New South Wales, Australia. Plant Soil 345:47–58
Singh BP, Hatton BJ, Singh B, Cowie AL, Kathuria A (2010) Influence of biochars on nitrous oxide emission and nitrogen leaching from two contrasting soils. J Environ Qual 39:1224–1235
Slavich PG, Sinclair K, Morris SG, Kimber SWL, Downie A, Van Zwieten L (2013) Contrasting effects of manure and green waste biochars on the properties of an acidic ferralsol and productivity of a subtropical pasture. Plant Soil 366:213–227
Smith JL, Collins HP, Bailey VL (2010) The effect of young biochar on soil respiration. Soil Biol Biochem 42:2345–2347
Sohi SP, Krull E, Lopez-Capel E, Bol R (2010) A review of biochar and its use and function in soil. Adv Agron 105:47–82
Soinne H, Hovi J, Tammeorg P, Turtola E (2014) Effect of biochar on phosphorus sorption and clay soil aggregate stability. Geoderma 219–220:162–167
Spokas KA (2013) Impact of biochar field aging on laboratory greenhouse gas production potentials. GCB Bioenergy 5:165–176
Stavi I, Lal R (2013) Agroforestry and biochar to offset climate change: a review. Agron Sustain Dev 33:81–96
Steinbeiss S, Gleixner G, Antonietti M (2009) Effect of biochar amendment on soil carbon balance and soil microbial activity. Soil Biol Biochem 41:1301–1310
Steiner C, Teixeira WG, Lehmann J, Nehls T, Macedo JLV, Blum WEH, Zech W (2007) Long term effects of manure, charcoal and mineral fertilization on crop production and fertility on a highly weathered Central Amazonian upland soil. Plant Soil 291:275–290
Sun FF, Lu SG (2014) Biochars improve aggregate stability, water retention, and pore-space properties of clayey soil. J Plant Nutr Soil Sci 177:26–33
Sun LY, Li L, Chen ZZ, Wang JY, Xiong ZQ (2014) Combined effects of nitrogen deposition and biochar application on emissions of N2O, CO2 and NH3 from agricultural and forest soils. Soil Sci Plant Nutr 60:254–265
Thomas SC, Gale N (2015) Biochar and forest restoration: a review and meta-analysis of tree growth responses. New For 46:931–946
Tian D, Qu ZY, Gou MM, Li B, Lv YJ (2015) Experimental study of influence of biochar on different texture soil hydraulic characteristic parameters and moisture holding properties. Pol J Environ Stud 24:1435–1442
Tonks AJ, Aplin P, Beriro DJ, Cooper H, Evers S, Vane CH, Sjögersten S (2017) Impacts of conversion of tropical peat swamp forest to oil palm plantation on peat organic chemistry, physical properties and carbon stocks. Geoderma 289:36–45
Topoliantz S, Ponge JF, Ballof S (2005) Manioc peel and charcoal: a potential organic amendment for sustainable soil fertility in the tropics. Biol Fertil Soils 41:15–21
Tsai WT, Lee MK, Chang YM (2007) Fast pyrolysis of rice husk: product yields and compositions. Bioresour Technol 98:22–28
Uchimiya M, Chang S, Klasson KT (2011) Screening biochars for heavy metal retention in soil: role of oxygen functional groups. J Hazard Mater 190:432–441
Uzoma KC, Inoue M, Andry H, Zahoor A, Nishihara E (2011) Influence of biochar application on sandy soil hydraulic properties and nutrient retention. J Food Agric Environ 9:1137–1143
Van Zwieten L, Kimber S, Morris S, Chan KY, Downie A, Rust J, Joseph S, Cowie A (2010a) Effects of biochar from slow pyrolysis of papermill waste on agronomic performance and soil fertility. Plant Soil 327:235–246
Van Zwieten L, Kimber S, Morris S, Downie A, Berger E, Rust J, Scheer C (2010b) Influence of biochars on flux of N2O and CO2 from Ferrosol. Soil Res 48:555–568
Wang H, Lin K, Hou Z, Richardson B, Gan J (2010) Sorption of the herbicide terbuthylazine in two New Zealand forest soils amended with biosolids and biochars. J Soils Sediments 10:283–289
Wang JY, Zhang M, Xiong ZQ, Liu PL, Pan GX (2011) Effects of biochar addition on N2O and CO2 emissions from two paddy soils. Biol Fertil Soils 47:887–896
Wang C, Tu Q, Dong D, Strong PJ, Wang H, Sun B, Wu W (2014a) Spectroscopic evidence for biochar amendment promoting humic acid synthesis and intensifying humification during composting. J Hazard Mater 280:409–416
Wang ZL, Li YF, Chang SX, Zhang JJ, Jiang PK, Zhou GM, Shen ZM (2014b) Contrasting effects of bamboo leaf and its biochar on soil CO2 efflux and labile organic carbon in an intensively managed Chinese chestnut plantation. Biol Fertil Soils 50:1109–1119
Wang JY, Xiong ZQ, Kuzyakov Y (2016) Biochar stability in soil: meta-analysis of decomposition and priming effects. GCB Bioenergy 8:512–523
Wang ZY, Chen L, Sun FL, Luo XX, Wang HF, Liu GC, Xu ZH, Jiang ZX, Pan B, Zheng H (2017) Effects of adding biochar on the properties and nitrogen bioavailability of an acidic soil. Eur J Soil Sci 68:559–572
West TO, McBride AC (2005) The contribution of agricultural lime to carbon dioxide emissions in the United States: dissolution, transport, and net emissions. Agric Ecosyst Environ 108:145–154
Wood TE, Cavaleri MA, Reed SC (2012) Tropical forest carbon balance in a warmer world: a critical review spanning microbial-to ecosystem-scale processes. Biol Rev 87:912–927
Woolf D, Lehmann J (2012) Modelling the long-term response to positive and negative priming of soil organic carbon by black carbon. Biogeochemistry 111:83–95
Wrobel-Tobiszewska A, Boersma M, Adams P, Singh B, Franks S, Sargison JE (2016) Biochar for eucalyptus forestry plantations. Acta Hortic 1108:55–62
Wu W, Yang M, Feng Q, McGrouther K, Wang H, Lu H, Chen Y (2012) Chemical characterization of rice straw-derived biochar for soil amendment. Biomass Bioenergy 47:268–276
Xiao YH (2016) Effects of different application rates of biochar on the soil greenhouse gas emission in Chinese chestnut stands. Master Thesis, Zhejiang A & F University, Hangzhou, Zhejiang (in Chinese).
Xiao Q, Zhu LX, Zhang HP, Li XY, Shen YF, Li SQ (2016a) Soil amendment with biochar increases maize yields in a semi-arid region by improving soil quality and root growth. Crop Pasture Sci 67:495
Xiao YH, Li YF, Wang ZL, Jiang PK, Zhou GM, Liu J (2016b) Effects of bamboo leaves and their biochar additions on soil N2O flux in a chinese chestnut forest. J Plant Nutr Fert 22:697–706 (in Chinese)
Xu M, Shang H (2016) Contribution of soil respiration to the global carbon equation. J Plant Physiol 203:16–28
Xu QF, Jiang PK, Xu ZH (2008) Soil microbial functional diversity under intensively managed bamboo plantations in southern China. J Soils Sediments 8:177
Xu CY, Hosseini-Bai S, Hao Y, Rachaputi RCN, Wang H, Xu Z, Wallace H (2015) Effect of biochar amendment on yield and photosynthesis of peanut on two types of soils. Environ Sci Pollut Res 22:6112–6125
Xu Y, Seshadri B, Sarkar B, Wang H, Rumpel C, Sparks D, Farrell M, Hall T, Yang X, Bolan N (2018) Biochar modulates heavy metal toxicity and improves microbial carbon use efficiency in soil. Sci Total Environ 621:148–159
Yanai Y, Toyota K, Okazaki M (2007) Effects of charcoal addition on N2O emissions from soil resulting from rewetting air-dried soil in short-term laboratory experiments. Soil Sci Plant Nutr 53:181–188
Yang X, Liu J, McGrouther K, Huang H, Lu K, Guo X, He L, Lin X, Che L, Ye Z, Wang H (2016) Effect of biochar on the extractability of heavy metals (Cd, Cu, Pb, and Zn) and enzyme activity in soil. Environ Sci Pollut Res 23:974–984
Yang X, Lu K, McGrouther K, Che L, Hu G, Wang Q, Liu X, Shen L, Huang H, Ye Z, Wang H (2017) Bioavailability of Cd and Zn in soils treated with biochars derived from tobacco stalk and dead pigs. J Soils Sediments 17:751–762
Yoo G, Kang H (2012) Effects of biochar addition on greenhouse gas emissions and microbial responses in a short-term laboratory experiment. J Environ Qual 41:1193–1202
Yu LQ, Tang J, Zhang RD, Wu QH, Gong MM (2013) Effects of biochar application on soil methane emission at different soil moisture levels. Biol Fertil Soils 49:119–128
Yuan JH, Xu RK (2011) The amelioration effects of low temperature biochar generated from nine crop residues on an acidic ultisol. Soil Use Manag 27:110–115
Yuan JH, Xu RK, Qian W, Wang RH (2011) Comparison of the ameliorating effects on an acidic ultisol between four crop straws and their biochars. J Soils Sediments 11:741–750
Yuan Y, Bolan N, Prévoteau A, Vithanage M, Biswas JK, Ok YS, Wang H (2017) Applications of biochar in redox-mediated reactions. Bioresour Technol 246:271–281
Zhang AF, Zhou X, Li M, Wu HM (2017) Impacts of biochar addition on soil dissolved organic matter characteristics in a wheat-maize rotation system in Loess Plateau of China. Chemosphere 186: 986–993
Zhang AF, Liu YM, Pan GX, Hussain Q, Li LQ, Zheng JW, Zhang XH (2012) Effect of biochar amendment on maize yield and greenhouse gas emissions from a soil organic carbon poor calcareous loamy soil from Central China Plain. Plant Soil 351:263–275
Zhang X, Wang H, He L, Lu K, Sarmah A, Li J, Bolan N, Pei J, Huang H (2013) Using biochar for remediation of soils contaminated with heavy metals and organic pollutants. Environ Sci Pollut Res 20:8472–8483
Zhang X, He L, Sarmah AK, Lin K, Liu Y, Li J, Wang H (2014) Retention and release of diethyl phthalate in biochar-amended vegetable garden soils. J Soils Sediments 14:1790–1799
Zhang K, Chen L, Li Y, Brookes PC, Xu JM, Luo Y (2016a) The effects of combinations of biochar, lime, and organic fertilizer on nitrification and nitrifiers. Biol Fertil Soils 53:77–87
Zhang X, Sarmah AK, Bolan NS, He L, Lin X, Che L, Tang C, Wang H (2016b) Effect of aging process on adsorption of diethyl phthalate in soils amended with bamboo biochar. Chemosphere 142:28–34
Zhao L, Cao XD, Mašek O, Zimmerman A (2013) Heterogeneity of biochar properties as a function of feedstock sources and production temperatures. J Hazard Mater 256:1–9
Zheng J, Chen J, Pan G, Liu X, Zhang X, Li L, Bian R, Cheng K, Jinwei Z (2016) Biochar decreased microbial metabolic quotient and shifted community composition four years after a single incorporation in a slightly acid rice paddy from southwest China. Sci Total Environ 571:206–217
Zhou GM, Xu JM, Jiang PK (2006a) Effect of management practices on seasonal dynamics of organic carbon in soils under bamboo plantations. Pedosphere 16:525–531
Zhou GY, Liu SG, Li ZA, Zhang DQ, Tang XL, Zhou CY, Yan JH, Mo JM (2006b) Old-growth forests can accumulate carbon in soils. Science 314:1417–1417
Zhou GY, Zhou XH, Zhang T, Du ZG, He YH, Wang XH, Shao JJ, Cao Y, Xue SG, Wang HL, Xu CY (2017) Biochar increased soil respiration in temperate forests but had no effects in subtropical forests. Forest Ecol Manag 405:339–349
Acknowledgements
This study was supported by the National Natural Science Foundation of China (31470626, 41401318, 21577131), the Natural Science Foundation for Distinguished Young Scholar of Zhejiang Province (LR18C160001), the Natural Science Foundation of Zhejiang Province, China (LY14C160007, LZ15D010001), the Natural Science Foundation of Guangdong Province, China (2017A030311019), the Major Science and Technology Project in Zhejiang Province, China (2015C03019), and the Special Funding for the Introduced Innovative R&D Team of Dongguan, China (2014607101003).
Author information
Authors and Affiliations
Corresponding author
Additional information
Responsible editor: Zhihong Xu
Rights and permissions
About this article
Cite this article
Li, Y., Hu, S., Chen, J. et al. Effects of biochar application in forest ecosystems on soil properties and greenhouse gas emissions: a review. J Soils Sediments 18, 546–563 (2018). https://doi.org/10.1007/s11368-017-1906-y
Received:
Accepted:
Published:
Issue Date:
DOI: https://doi.org/10.1007/s11368-017-1906-y