Hindawi Applied and Environmental Soil Science Volume 2019, Article ID 5794869, 9 pages https://doi.org/10.1155/2019/5794869 Review Article The Role of Soil pH in Plant Nutrition and Soil Remediation Dora Neina Department of Soil Science, P.O. Box LG 245, School of Agriculture, College of Basic and Applied Science, University of Ghana, Legon-Accra, Ghana Correspondence should be addressed to Dora Neina; dneina@gmail.com Received 26 August 2019; Accepted 5 October 2019; Published 3 November 2019 Academic Editor: Marco Trevisan Copyright © 2019 Dora Neina.(is is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. In the natural environment, soil pH has an enormous influence on soil biogeochemical processes. Soil pH is, therefore, described as the “master soil variable” that influences myriads of soil biological, chemical, and physical properties and processes that affect plant growth and biomass yield. (is paper discusses how soil pH affects processes that are interlinked with the biological, geological, and chemical aspects of the soil environment as well as how these processes, through anthropogenic interventions, induce changes in soil pH. Unlike traditional discussions on the various causes of soil pH, particularly soil acidification, this paper focuses on relationships and effects as far as soil biogeochemistry is concerned. Firstly, the effects of soil pH on substance availability, mobility, and soil biological processes are discussed followed by the biogenic regulation of soil pH. It is concluded that soil pH can broadly be applied in two broad areas, i.e., nutrient cycling and plant nutrition and soil remediation (bioremediation and physicochemical remediation). 1. Introduction greatest impact on the components of human well-being in terms of safety, the basic material for a good life, health, and To many, soil pH is only essential for the chemistry and good social relations. fertility of soils. However, the recognition of soil functions In the natural environment, the pH of the soil has an beyond plant nutrient supply and the role soil as a medium enormous influence on soil biogeochemical processes. Soil of plant growth required the study of the soil and its pH is, therefore, described as the “master soil variable” that properties in light of broader ecosystem functions through a influences myriads of soil biological, chemical, and physical multidisciplinary approach. (is allows scientists to view properties and processes that affect plant growth and bio- processes from landscape to regional and global levels. One mass yield [6, 7]. Soil pH is compared to the temperature of a process that denotes the multidisciplinary approach to soil patient during medical diagnoses because it readily gives a science is soil biogeochemistry, which studies bio- hint of the soil condition and the expected direction of many geochemical processes. (e ecosystem functions of soil, to soil processes (lecture statement, Emeritus Prof. Eric Van some extent, have a strong relationship with soil bio- Ranst, Ghent University). For instance, soil pH is controlled geochemical processes, which are linkages between bi- by the leaching of basic cations such as Ca, Mg, K, and Na far ological, chemical, and geological processes [1]. (e soil is beyond their release from weathered minerals, leaving H+ the critical element of life support systems because it delivers and Al3+ ions to dominant exchangeable cations; the dis- several ecosystem goods and services such as carbon storage, solution of CO2 in soil water producing carbonic acid, which water regulation, soil fertility, and food production, which dissociates and releases H+ ions; humic residues from the have effects on human well-being [2–4]. (ese ecosystem humification of soil organic matter, which produces high- goods and services are broadly categorized as supporting, density carboxyl and phenolic groups that dissociate to provisioning, regulating, and cultural services [5]. According release H+ ions; nitrification of NH + to NO − produces H+4 3 to the Millennium Ecosystem Assessment [5], the pro- ions; removal of N in plant and animal products; and inputs visioning and regulating functions are said to have the from acid rain and N uptake by plants [8]. On the other 2 Applied and Environmental Soil Science hand, pH controls the biology of the soil as well as biological Biodegradation processes. Consequently, there is a bidirectional relationship of organic between soil pH and biogeochemical processes in terrestrial pollutants ecosystems, particularly in the soil. In this sense, the soil pH Mineralisation Rhizosphere influences many biogeochemical processes, whereas some of organic processes biogeochemical processes, in turn, influence soil pH, to some matter extent, as summarised in Figure 1. Organic For many decades, intensive research has revealed that Ammonia amendments volatilisation soil pH influences many biogeochemical processes. Recent Soil advances in research have made intriguing revelations about Precipitation: pH Dissolution: the important role of soil pH in many soil processes. (is organic matter, organic matter,heavy metals important soil property controls the interaction of xeno- heavy metals biotics within the three phases of soil as well as their fate, Soil enzyme Nitrification translocation, and transformation. Soil pH, therefore, de- activities and termines the fate of substances in the soil environment. (is denitrification has implications for nutrient recycling and availability for Microbial crop production, distribution of harmful substances in the ecophysiologicalindicators environment, and their removal or translocation. (is functional role of soil pH in soil biogeochemistry has been Figure 1: Some biogeochemical processes and their relations with exploited for the remediation of contaminated soils and the soil pH. control of pollutant translocation and transformation in the environment. Unfortunately, in many studies, soil pH is and 53%, respectively. In contrast, he found that 50% of Cd often measured casually as a norm without careful con- and Zn sorbed onto humic acids between pH 4.8–4.9 [13]. sideration for its role in soil. (is paper seeks to explore the (e fate of readily available trace elements depends on both importance of pH as an indicator of soil biogeochemical the properties of their ionic species formed in the soil so- processes in environmental research by discussing the lution and that of the chemical system of soil apart from soil biogeochemical processes that are influenced by soil pH, the pH itself [14]. Research has established that with increasing biogeochemical processes that also control soil pH, and the soil pH, the solubility of most trace elements will decrease, relevance of the relationship for future research, planning, leading to low concentrations in soil solution [14]. Any and development. increase or decrease in soil pH produces distinct effects on metal solubility. (is may probably depend on the ionic 2. Biogeochemical Processes Influenced by species of the metals and the direction of pH change. Rengel Soil pH [15] observed that the solubility of divalent metals decreases a hundred-fold while trivalent ones experience a decrease of up 2.1. Substance Translocation. Simultaneously, in accordance to a thousand-fold. In contrast, Förster [10] found that a with biochemical changes, physicochemical processes, in- decrease in soil pH by one unit resulted in a ten-fold increase cluding dissolution, precipitation, adsorption, dilution, in metal solubility. In an experiment, he observed that at pH volatilization, and others, influence leachate quality [9]. 7, only about 1mg Zn·L− 1 of the 1200mg·kg− 1 total Zn content was present in soil solution. At pH 6, the concen- tration reached 100mg Zn·L− 1 while at pH 5, 40mg Zn·L− 1 2.1.1. Trace Element Mobility. Soil pH controls the solubility, was present. Aside from adsorption, trace element concen- mobility, and bioavailability of trace elements, which de- trations at high soil pH may also be caused by precipitation termine their translocation in plants [10]. (is is largely with carbonates, chlorides, hydroxides, phosphate, and sul- dependent on the partition of the elements between solid and phates [11, 16]. Apatite and lime applied to soils produced the liquid soil phases through precipitation-dissolution reactions highest effect on pH and simultaneously decreased the [10, 11] as a result of pH-dependent charges in mineral and concentrations of available, leachable, and bioaccessible Cu organic soil fractions. For instance, negative charges domi- and Cd [16]. nate in high pH whereas positive charges prevail in low pH values [12]. Additionally, the quantity of dissolved organic carbon, which also influences the availability of trace ele- 2.1.2. Mobility of Soil Organic Fractions. Soil organic matter ments, is controlled by soil pH. At low pH, trace elements are exists in different fractions ranging from simple molecules usually soluble due to high desorption and low adsorption. At such as amino acids, monomeric sugars, etc. to polymeric intermediate pH, the trend of trace element adsorption in- molecules such as cellulose, protein, lignin, etc. (ese occur creases from almost no adsorption to almost complete ad- together with undecomposed and partly decomposed plant sorption within a narrow pH range called the pH-adsorption and microbial residues [17]. (e solubility and mobility of edge [13]. From this point onwards, the elements are the fractions differ during and after decomposition and completely adsorbed [13]. For instance, Bradl [13] found that could lead to the leaching of dissolved organic carbon and at pH 5.3, the adsorption of Cd, Cu, and Zn onto a sediment nitrogen in some soils. Dissolved organic carbon is defined composite consisting of Al-, Fe-, and Si-oxides was 60%, 62%, as the size of organic carbon that passes through a 0.45mm Applied and Environmental Soil Science 3 diameter filter [18]. Soil pH increases the solubility of soil 2.2.2. Soil Enzyme Activities. Extracellular enzymes are organic matter by increasing the dissociation of acid produced by soil microorganisms for the biogeochemical functional groups [19] and reduces the bonds between the cycling of nutrients [33]. Soil pH is essential for the proper organic constituents and clays [20]. (us, the content of functioning of enzyme activity in the soil [34, 35], and may dissolved organic matter increases with soil pH and con- indirectly regulate enzymes through its effect on the mi- sequently mineralizable C and N [20]. (is explains the crobes that produce them [36]. However, there are myriad of strong effects of alkaline soil pH conditions on the leaching enzymes in biological systems which assist in the trans- of dissolved organic carbon and dissolved organic nitrogen formation of various substances. Besides, enzymes are of observed in many soils containing substantial amounts of different origins and with differing degrees of stabilization organic matter [19, 21].(e same observation has beenmade on solid surfaces. (us, the pH at which they reach their on the dissolved organic carbon concentration in peatland optimum activity (pH optima) is likely to differ [33]. It is soils [22]. (e pH-dependence of dissolved organic carbon striking that enzymes that act on the same substrates could concentration gets more pronounced beyond pH 6 [23]. vary considerably in their pH optima. (is is evident in Within the pH condition in a specific soil system, the phosphorus enzymes, which have both acid and alkaline solubility of organic matter is strongly influenced by the type windows of functioning in the range of pH 3–5.5 and pH of base and is particularly greater in the presence of 8.5–11.5 [33]. In a study on the optimum pH for specific monovalent cations than with multivalent ones [23]. enzyme activity in soils from seven moist tropical forests in According to Andersson and Nilsson [24] and Andersson Central Panama, Turner [33] classified enzymes into three et al. [19], soil pH controls the solubility of organic matter in groups depending on their pH optima as found in the soils. two major ways: (i) its influence on the charge density of the (ese were: (a) enzymes with acidic optima that appeared humic compounds, and (ii) either the stimulation or re- consistent among soils, (b) enzymes with acidic pH optima pression of microbial activity. (e former is found to be that varied among the soils, and (c) enzymes with optima in more pronounced than the latter [19]. both acid and alkaline soil pH. Stursova and Walker [37] found that organophosphorus hydrolase has optimal activity at higher pH. For instance, glycosidases have an optimal pH 2.2. Soil Biological Processes range between 4 and 6 compared to proteolytic and oxidative enzymes whose optima was between 7 and 9 [35, 36, 38]. 2.2.1. Microbial Ecophysiological Indicators. Ecophysiology is Shifts in microbial community composition could poten- an interlinkage between cell-physiological functioning un- tially influence enzyme production if different microbial der the influence of environmental factors [25]. It is esti- groups require lower nutrient concentrations to construct mated using the metabolic quotient (qCO2) as an index [25] biomass, or have enzymes which differ in affinity for nu- to show the efficiency of organic substrate utilization by soil trients [39]. microbes in specific conditions [26]. A decrease in microbial community respiration makes C available for more biomass production, which yields higher biomass per unit [27]. (e 2.2.3. Biodegradation. Soil microorganisms are described as metabolic quotient is, therefore, described as a cell-physi- ecosystem engineers involved in the transformation of sub- ological entity that reflects changes in environmental con- stances in the soil. One of such transformations is bio- ditions [25]. (is implies that any change in environmental degradation, a process through which microbes remediate conditions towards the adverse state will be indicated by the contaminated soils by transforming toxic substances and index [25]. (is is controlled by soil pH [28]. Soil pH as a xenobiotics into least or more toxic forms. Biodegradation is driving force for microbial ecophysical indices stems from the chemical dissolution of organic and inorganic pollutants its influence on the microbial community together with the by microorganisms or biological agents [34, 40]. Like many maintenance demands of the community [28] and was soil biological processes, soil pH influences biodegradation among the predictors of the metabolic quotient [29, 30]. (e through its effect on microbial activity, microbial community metabolic quotient was found to be two-and-a-half times and diversity, enzymes that aid in the degradation processes as higher in low pH soils compared to neutral pH soils [28]. well as the properties of the substances to be degraded. Soil (is has been associated with the divergence of the internal pHwas themost important soil property in the degradation of cell pH (usually kept around 6.0) from the surrounding pH atrazine [41]. Generally, alkaline or slightly acid soil pH conditions, which increases the maintenance requirements enhances biodegradation, while acidic environments pose and reduces total microbial biomass produced [25]. limitations to biodegradation [34, 37, 42]. Usually, pH values It is observed from the literature that soil pH conditions between 6.5 and 8.0 are considered optimum for oil degra- required for microbial activity range from 5.5–8.8 dation [43]. Within this range, specific enzymes function [26, 31, 32]. (us, soil respiration often increases with soil within a particular pH spectrum. For instance, the pesticide pH to an optimum level [26]. (is also correlates with fenamiphos degraded in two United Kingdom soils with high microbial biomass C and N contents, which are often higher pH (>7.7) and two Australian soils with pH ranging from pH above pH 7 [26]. In low pH conditions, fungal respiration is 6.7 to 6.8. (e biodegradation process rather slowed down in usually higher than bacterial respiration and the vice versa three acidic United Kingdom soils (pH 4.7 to 6.7) in 90 days [25] because fungi are more adapted to acidic soil conditions after inoculation [42]. Xu [44] found some strains of bacteria than bacteria. isolated from petroleum-contaminated soil in northern China 4 Applied and Environmental Soil Science being able to degrade over 70% of petroleum at pH 7 and 9. In denitrification rate where the ratio of N2/N2O increased a degradation experiment involving polycyclic aromatic hy- exponentially with an increase in soil pH. (is is because drocarbons (PAHs), half of the PAHs degraded at pH 7.5 low pH prevents the assembly of functional nitrous oxide within seven days representing the highest amount degraded reductase, the enzyme reducing N2O to N2 in de- [34]. (is was associated with the highest bacterial pop- nitrification [15, 20] and this mostly depends on the natural ulations [34]. Furthermore, Houot et al. [41] found increased soil pH [49]. However, the soil pH at which the highest degradation of atrazine in French and Canadian soils, which activity of nitrous oxide reductase occurred was around pH occurred with increased soil pH. (ey observed maximum 7.3. (is occurred in soils amended with potassium hy- soil respiration in atrazine-contaminated soils at soil pH droxide (KOH) [51]. (is suggests the inhibition of de- values higher than 6.5 compared to those with soil pH value nitrification at high pH, particularly up to pH 9 [50]. less than 6.0 where metabolites rather accumulated. Furthermore, maximum denitrification of between 68% and 85% occurred in a sandy and a loamy soil with pH 5.2 2.2.4. Mineralization of Organic Matter. Organic matter and 5.9, respectively [52]. (e optimum pH for long-term mineralization is often expressed as carbon (C), nitrogen potential denitrification was between 6.6 and 8.3. Addi- (N), phosphorus (P), and sulphur (S) mineralization tionally, the short-term denitrifying enzyme activity through microbial action. Soil pH controls mineralization in depended on the natural soil pH [49]. (e effect of soil pH soils because of its direct effect on the microbial population on denitrification is partly due to pH controls over the and their activities. (is also has implications for the denitrifying microbial populations. (e population size of functions of extracellular enzymes that aid in the microbial the resident nitrate-reducing bacterial population in- transformation of organic substrates. Additionally, at a creased dramatically when the pH of the acid soil was higher soil pH, the mineralizable fractions of C and N in- increased [53]. crease because the bond between organic constituents and clays is broken [20]. In a study on the mineralization of C 2.2.6. Ammonia Volatilization. (e volatilization of am- and N in different upland soils of the subtropics treated with monia is a phenomenon that occurs naturally in all soils [54] different organic materials, Khalil et al. [45] found that soil and has been attributed to the dissociation of NH + to NH3 pH and C/N ratio were responsible for 61% of the de- 4and H+ shown in equation (1) [55] composition rate, with corresponding increases in CO2 ef- + + fluxes, net N mineralization, and net nitrification in alkaline NH4 ⟷NH3 + H (1) than in acid soils. Similar results had earlier on been ob- (e dissociation approaches equilibrium through the tained by Curtin et al. [20]. acidification of the medium. (e rate of acidification de- pends on the initial and final concentrations of ammonium 2.2.5. Nitrification and Denitrification. Nitrification and as well as on the buffering capacity of the medium [55]. denitrification are important nitrogen transformation pro- When solution pH increases above 7, H+ is consumed in the cesses of environmental concern. Like many of the bio- reaction. (us, the dissociation of ammonium to ammonia geochemical processes, the processes, to a large extent, are in equation (1) will favour ammonia volatilization. In neutral controlled by soil pH. Nitrification involves the microbial and acid soils, NH −4 containing fertilizers are less subject to conversion of ammonium to nitrate. It generally increases NH3 loss than urea and urea-containing fertilizers [54]. with increasing soil pH but reaches an optimum pH [45–47]. However, the degree will also depend on the specific fer- In a four-year study, Kyveryga et al. [47] observed that soil tilizer and its effect on soil pH. In a study involving ammonia pH range of 6 to 8 strongly influenced the nitrification rates volatilization from an alkaline salt-affected soil cultivated of fertilizer N. Generally, the nitrification rate decreases at with rice, Li et al. [56] found that ammonia volatilization lower soil pH values. In some soils, nitrification and nitri- increased rapidly with pH and peaked at pH 8.6. Ammonia fication potential substantially decrease or are negligible volatilization is strongly correlated with pH and calcium below a pH value of 4.2. However, nitrification may still carbonate, which suggested that the soil pH was a key factor occur even below pH 4.14, suggesting that ammonia-oxi- in ammonia volatilization because calcium carbonate in- dizing and nitrifier communities might remain active at low creases soil pH which in turn controls the concentration of soil pH [48]. ammonia and ammonium in soil solution [57]. Denitrification is the microbiological process in which oxidized N species such as nitrate (NO −3 ) and nitrite 3. Biogenic Regulation of Soil pH (NO −2 ) are reduced to gaseous nitric oxide (NO), nitrous oxide (N2O), and molecular nitrogen (N2) under limited Soil biological processes from living organisms and bio- oxygen conditions [49]. Soil pH affects denitrification rate, chemical transformations of the remains of dead organisms potential denitrification, and the ratio between the two induce changes in soil pH. (is can either occur through the main products of denitrification (N2O and N2). (e ratio direct effect of biochemical processes occurring in the living has an inverse relation with soil pH [49]. At pH values organisms in the soil system, mostly through rhizosphere below 7, N2O was the main denitrification product whereas processes or through the direct and indirect effects of applied N2 prevailed at pH values above 8 [49]. Sun et al. [50] organic residues, whether in unburnt, burnt, or charred discovered that soil pH was the best predictor of forms as well as their decomposition. Applied and Environmental Soil Science 5 3.1. Rhizosphere Processes. (e rhizosphere is the volume of plants [67]. (is was revealed in an experiment on apple trees soil in the neighbourhood of roots that is influenced by root (Malus pumila Miller), buckwheat (Fagopyrum esculentum andmicrobial activities [58–60] Hiltner 1904 cited by [60]. It Moench), corn (Zeamays L.), cowpeas (Vigna unguiculata (L) is a longitudinal and radial gradient [61], ranging from 0 to Walp.), kaffir lime (Citrus hystrixDC.), lettuce (Lactuca sativa 2.0mm from the root mat [62, 63]. In this small soil volume, L.), pine trees (Pinus sp. L.), and wheat (Triticum aestivum L.), roots take up water and nutrients, undergo root elongation where Metzger [66] found maximum concentrations of and expansion, release exudates, respire, and thus have HCO −3 in the rhizosphere during the blooming and fruiting higher microbial activity [59, 63]. (rough some of these stages (Figure 2), which was 10–29% higher compared to the biological processes, plant roots have the ability to induce bulk soil. (e concentrations of HCO −3 in the rhizosphere of pH changes in the rhizosphere either by releasing protons the plants was in the order, lettuce� buckwheat> pine> (H+) or hydroxyl ions (OH− ) to maintain ion balance apple> kaffir> cowpeas> corn>wheat. (ese values were [58, 64], depending on the nutritional status of the plants much lower than those obtained in the rhizosphere of soybean [65]. (erefore, rhizosphere pH could increase or decrease (Glycine max (L.) Merr.) [64]. Furthermore, Turpault et al. depending on the prevailing process and types of ions [59] found that 93% of NO3-N was taken up by a Douglas fir released. (Pseudotsuga menziesii (Mirb.) Franco) stands during Plant root-induced soil pH change in the rhizosphere is April–September compared to 83% uptake during the Oc- controlled by specific processes and factors such as (i) ion tober-March period.(is likely increased rhizosphere pH and uptake coupled with the release of inorganic ions that implies that during periods of low nitrate uptake, soil pH maintain electroneutrality, (ii) the excretion of organic acid may decrease due to buffering or due to a response to the anions, (iii) root exudation and respiration, (iv) redox- uptake of NH −4 . coupled processes, (v) microbial production of acids after the assimilation of released root carbon, and (vi) plant genotype [58, 59]. Surprisingly, roots have a greater ten- 3.2. Raw and Combusted Organic Materials. When unburnt dency to raise the pH of the rhizosphere rather than lower it organic materials or raw plant residues are applied to the [65, 66]. (e dominant mechanism responsible for pH soil, the pH increases to a peak and decrease afterwards. For changes in the rhizosphere is plant uptake of nutrients in the instance, Forján et al. [68] found initial increases in soil pH form of cations and anions [58, 59, 65], primarily due to when they applied a mixture of sludge from a bleach plant, plant uptake of the two major forms of inorganic nitrogen urban solid waste and mine wastes, and a mixture of sludge (NH +4 and NO −3 ), which is usually taken up in large from a purification plant, wood chips, and remnants from quantities [59]. Nitrogen is taken up by plants in three major agri-food industries to the soil. Furthermore, the addition of forms: ammonium (NH +4 ), nitrate (NO −3 ), and molecular young Kikuyu (Pennisetum clandestinum L.) shoots also nitrogen (N2) [59], although amino acids can also be taken increased soil pH by up to one pH unit [69]. (e major up [58]. (e uptake of each of the three forms of nitrogen causes of this pH change is due to the (i) release of excess accompanies the release of corresponding ions to maintain residue alkalinity attributed to the basic cations such as Ca, electroneutrality in the rhizosphere. When nitrate domi- K, Mg, and Na [70]; (ii) decarboxylation of organic anions nates in soil or when its uptake dominates, plants must that occurs during C mineralisation, causing the con- release bicarbonate (HCO −3 ) or hydroxyl ions (OH − ) to sumption of protons and release of OH− [71, 72]; (iii) maintain electrical neutrality across the soil-root interface ammonification of the residue N; (iv) nitrification of min- resulting in rhizosphere pH increase [58, 59, 64]. In contrast, eralised residue N; and (v) association/dissociation of or- protons are released by plants in response to NH +4 uptake, ganic compounds [70]. (ese processes are determined by causing a decrease in rhizosphere pH [58, 62]. It has been the quantity applied and the prevailing soil and environ- revealed that 15, 6, and 0%, respectively, of the NH −4 N from mental conditions [70]. According to Xu et al. [70]; direct the total N present in the soil is required to decrease rhi- chemical reactions and oxidation of the organic anions zosphere pH decrease by 1.2 units, maintain it, or increase it during residue decomposition are the main mechanisms by 0.4 pH unit [62]. involved in organic anion-induced soil pH increase. Ad- (e extent of effects of the processes and factors con- ditionally, organic anions and other negatively charged trolling rhizosphere pH change depends on plant species and chemical functional groups present in organic matter can growth stages [65]. For instance, in a study on rhizosphere undergo association reactions with H+ ions [71, 73]. acidification interactions, Faget et al. [67] found differences (e increase in soil pH after residue application also between rhizosphere acidification in maize (Zea mays L.) and depends on the type of residue (either from monocots or beans (Phaseolus vulgaris L.). Maize initially acidified the dicots), which is related to the amount of alkalinity present, rhizosphere and gradually alkalized it over time while beans residue quality (C/N ratio), the rate of residue application showed opposite effects. (ey found an interaction effect of and decomposition, the initial pH, and buffering capacity of the two plant species on the rhizosphere pH change whereby the soil [70, 71]. Different residues have different chemical the degree of acidification or alkalization was weaker when and biochemical compositions, which determine the pro- roots grew within the same neighbourhood than when the cesses responsible for soil pH change.(is was detected in an roots were not growing near each other. However, the rhi- incubation experiment involving three soils and five dif- zosphere pH changes with time as a result of variable uptake ferent residue types where soil pH increased according to of nitrogen ions, plant species, and their growth stages of the lucerne> chickpea>medic>high-N wheat> low-N wheat [70]. 6 Applied and Environmental Soil Science 350 in the more acidic Podzol. (is peaked at 14 days after application and declined afterwards. However, in a field 300 study on the same soils [74], the application of chickpea residue increased soil pH by 1.3 units in both soils and 250 reached a maximum at 3 months, whereas canola residue 200 increased pH by 0.82 and 1.02 units in the Podzol and Cambisol, respectively, and reached a maximum pH at 9 150 months. Similar to unburnt organic materials, burnt or charred 100 plant residues contain a larger amount of alkalinity due to the volatilization of organic constituents under thermal 50 conditions leading to the concentration of alkaline con- stituents. (e actual alkalinity depends on the type of bio- 0 mass involved, their origin, and burnt temperature. Burnt and charred forms of organic materials include biochar and ash. Biochar is a solid consistent product pyrolysis, while ash is a loose powdery material obtained by combustion.(e pH Plants of biochar produced at 500–600°C was 6.4–9.3 and showed a Rhizosphere strong relationship with the total alkalinity (i.e., organic and Bulk soil inorganic alkalinities) [75]. (e inorganic alkalinity in- Figure 2: (e compositions of bicarbonate as found in the rhi- creased with increasing pyrolysis temperature and with zosphere and bulk soil of some plants grown in a greenhouse. Error increasing divalent cation contents [75] because the organic bars are± one standard deviation (n� 2 to 34). Lettuce and pine constituents volatilize during pyrolysis. (is alkalinity of had only data one data point each and could not be presented with biochar neutralizes acidity and increases soil pH depending error bars (data from [66]). on the amount of alkalinity and soil buffering capacity [76]. Biomass ash contains substantial alkalinity, which is often Furthermore, in a 59-day laboratory incubation [71] and field expressed as percent calcium carbonate equivalence (% experiments [74], it was found that the magnitude of soil pH CCE). It ranges from 17–95% [77, 78]. Similarly to biochar, increase following residue amendment was in the order the combustion temperature has effects on the alkalinity of chickpea> canola>wheat [71, 74]. (ey observed that 40–62% biomass aside the biomass type and source. Recently, Neina of soluble alkalinity in canola and chickpea residues were re- et al. (submitted) found that ash from charcoal had higher sponsible for the pH increases. It is obvious from these, and CCE, pH, and K contents than firewood ash. Depending on many other studies [69], that the residues of dicots, particularly the alkalify and buffering capacity of the soil receiving the legumes, have high alkalinity and produce larger effects on soil biomass ash, soil pH increase can be high or low. For in- pH change than monocots. (e pH increase after residue ad- stance, in two Ghanaian Acrisols, biomass ash applied at dition often reaches a peak and declines thereafter as a result of 2.5 g·kg− 1 soil increased soil pH by about 1 unit after 12 nitrification. Residues with low carbon-nitrogen (C/N) ratios are weeks of laboratory incubation [79]. (is pH change is often associated with sharp pH decline after a certain period and mostly short-lived due to other biogeochemical processes. the extent varies with soil type and soil buffering capacity [70, 71, 74], whereas those with high C/N ratios produce smaller 4. Conclusions pH increase, or none at all [70]. (e initial pH and buffering capacity of soils receiving (e content of this paper highlights the role of soil pH as a plant residues have a profound role in the extent of pH master soil variable that has a bidirectional relationship with change after application. For instance, three soil types of soil biogeochemical processes. Although not all bio- different initial soil pH, namely, Wodjil sandy loam with geochemical processes were discussed in this paper, those pH(CaCl2) 3.87, Bodallin sandy loam soil with pH 4.54, and discussed have substantial influences on soil health, nutrient Lancelin sandy soil with pH 5.06, were incubated with availability, pollution, and potential hazards of pollutants as residues of chickpea, lucerne, medic, high-Nwheat, and low- well as their fate in the food chain. (e mobility of un- N wheat. (ereafter, the pH increased by about 3.3 units wholesome substances through the hydrological cycle can- with lucerne in the Wodjil soil (3.87), 1.6 with chickpea, 1.5 not be overlooked here because of the intimate relationship with medic, and 0.5 with high-N wheat, and no increase with between soil and water. (us, an understanding of this can low-N wheat. (e pH increased and peaked at 42 days of form a basis and a guide to decisions and choices of soil incubation for Bodallin andWodjil sandy loams followed by management, remediation, rehabilitation, and the mainte- a decline whereas, in the Lancelin sandy soil, the pH peaked nance of soil quality. (e observed soil pH-biogeochemistry at day 14 before declining [70]. In another incubation study relationships provide insight for future applications for [71], a Podzol with an initial pH of 4.5 and a Cambisol with increased yields for specific crops through nutrient recycling an initial pH of 6.2 were amended with residues of canola, and availability, which enhances crop growth. (e transient chickpea, and wheat. For all the residues, the pH increase in rhizosphere soil pH could also be used to enhance the the moderately acidic Cambisol was up to sixfold larger than availability of certain nutrients in certain soil conditions Bicarbonate content (mg·kg–1 soil) Apple Buckwheat Corn Cowpeas Kaffir Lettuce Pine Wheat Applied and Environmental Soil Science 7 [80]. More importantly, soil pH could be useful for soil [14] A. Kabata-Pendias, Trace Elements in Soils and Plants, CRC pollution control through the distribution and removal of Press, Boca Raton, FL, USA, 2011. harmful substances from systems. For instance, the min- [15] Z. Rengel, “Genotypic differences in micronutrient use effi- eralization and degradation processes such as those of C and ciency in crops,” Communications in Soil Science and Plant N mineralisation and the degradation of pesticide occur Analysis, vol. 32, no. 7-8, pp. 1163–1186, 2001. between pH 6.5 and 8, while the maximum degradation of [16] H. Cui, Y. Fan, G. Fang, H. Zhang, B. Su, and J. Zhou, petroleum and PAHs occur between pH 7 and 9. (ese, as “Leachability, availability and bioaccessibility of Cu and Cd ina contaminated soil treated with apatite, lime and charcoal: a well as pH maxima for various microbial enzymes, could be five-year field experiment,” Ecotoxicology and Environmental utilized in many soil remediation strategies, particularly in Safety, vol. 134, pp. 148–155, 2016. bioremediation. Ultimately, soil pH can broadly be applied [17] J. A. Baldock, “Composition and cycling of organic carbon in in two broad areas, i.e., nutrient cycling and plant nutrition soil,” inNutrient Cycling in Terrestrial Ecosystems, P. Marschner and soil remediation (bioremediation and physicochemical and Z. Rengel, Eds., pp. 1–35, Springer-Verlag, Berlin, Ger- remediation). many, 2007. [18] F. Vogel, J. Harf, A. Hug, and P. 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