Ion sorption on soil and sediment has been reported to be potentially affected by bacteria which may interact both physically and chemically with solid surfaces. However, whether and how bacteria affect the sorption of inorganic phosphate (P) on soil colloids remains poorly known. Here, we comparably investigated the P sorption on four soil colloids (three highly weathered soils including two Oxisols and one Ultisol and one weakly weathered soil Alfisol) and their complexes with Bacillus subtilis and Pseudomonas fluorescens. Batch experiments showed a notable reduction in P sorption on the colloids of highly weathered soils by the two bacteria at varying P concentrations and pHs; whereas that on the colloids of Alfisol appeared to be unaffected by the bacteria. The inhibitory effect was confirmed by both greater decline in P sorption at higher bacteria dosages and the ability of the bacteria to desorb P pre-adsorbed on the colloids. Further evidence was given by isothermal titration calorimetric experiments which revealed an alteration in enthalpy change caused by the bacteria for P sorption on Oxisol but not for that on Alfisol. The B. subtilis was more efficient in suppressing P sorption than the P. fluorescens, indicating a dependence of the inhibition on bacterium type. After association with bacteria, zeta potentials of the soil colloids decreased considerably. The decrease positively correlated with the decline in P sorption, regardless of soil and bacterium types, demonstrating that the increment in negative charges of soil colloids by bacteria probably contributed to the inhibition. In addition, scanning electron microscopic observation and the Derjaguin–Landau–Verwey–Overbeek theory prediction suggested appreciable physical and chemical interactions between the bacteria and the highly weathered soil colloids, which might be another contributor to the inhibition. These findings expand our understandings on how bacteria mobilize legacy P in soils and sediments.

Extracellular polymeric substances (EPS) found in soils can reduce the mobility of heavy metals through the use of both electrostatic and non-electrostatic mechanisms. Their effects vary from one soil type to another. The influence of EPS from Escherichia coli on the adsorption behaviors of Cu(II) and Cd(II) by two bulk variable charge soils, Oxisol and Ultisol, was studied at constant and varied pH, and the results were compared to a constant charge Alfisol. The maximum adsorption capacities of the soils were significantly (P < 0.05) enhanced in the presence of EPS, with Cu(II) adsorption being greater. Interaction of EPS with soils made the soil surface charge more negative by neutralizing positive charges and shifting the zeta potentials in a negative direction: from −18.6 to −26.4 mV for Alfisol, +5.1 to −22.2 mV for Oxisol, and +0.3 to −28.0 mV for Ultisol at pH 5.0. The adsorption data fitted both the Freundlich and Langmuir isotherms well. Preadsorbed Cd(II) was more easily desorbed by KNO₃ than preadsorbed Cu(II) from both the control and EPS treated soils. The adsorption of both metals was governed by electrostatic and non-electrostatic mechanisms, although more Cu(II) was adsorbed through the non-electrostatic mechanism. The information obtained in this study will improve our understanding of the mechanisms involved in reducing heavy metals mobility in variable charge soils and hence, their bioavailability.

Acidification in variable charge soils is on the rise due to increased acid deposition and use of nitrogenous fertilizers. The associated low pH and cation exchange capacity make the soils prone to depleted base cations and increased levels of Al³⁺. Consequently, Al toxicity to plants and soil infertility decrease crop yield. This study was designed to investigate the effect of Pseudomonas fluorescens on the acidification of two Ultisols. The simulated acidification experiment demonstrated that the pH of bacteria-treated soil was higher than that of control under similar conditions, suggesting that the adhered bacteria inhibited soil acidification. This observation was attributed to the association of organic anions (RCOO⁻ or RO⁻) on bacteria with H⁺ to form neutral molecules (RCOOH or ROH) and reducing the activity of H⁺ in solution. The bacteria also inhibited the increase in soil soluble Al and exchangeable Al during soil acidification. The adhesion of bacteria on the soils increased soil effective cation exchange capacity (ECEC) and exchangeable base cations at each pH compared to control. The release of exchangeable base cations from bacteria-treated soil, and the decrease in soil ECEC and exchangeable base cations with decreasing pH confirmed that protonation of organic anions on adhered bacteria was mainly responsible for the inhibition of soil acidification. The change of zeta potential of the bacteria with pH and the ART-FTIR analysis at various pH provided more evidence for this mechanism. Therefore, the bacteria in variable charge soils played an important role in retarding soil acidification.

The primary objective of this study was to identify the capacity and mechanism of extracellular polymeric substance (EPS) adsorption on soil colloids of Alfisol and Ultisol at different pH and ionic strengths. Two kinds of EPS were extracted from Bacillus subtilis and Pseudomonas fluorescens by centrifugation, and their adsorption on Ultisol and Alfisol was investigated using a batch adsorption experiment and attenuated total reflectance–Fourier transform infrared spectroscopy (ATR-FTIR). The average diameter of EPS from B. subtilis and P. fluorescens was 1825 and 1288 nm, respectively, and both the EPS were negatively charged. The zeta potentials of the two EPS became more negative with increasing solution pH from 3 to 8 and less negative with increasing ionic strength from 0 to 80 mM. The maximum adsorption capacity of EPS-C and EPS-N on Alfisol was higher than that on Ultisol, whereas the maximum adsorption capacity of EPS-P on Alfisol was lower than that on Ultisol. The adsorption of EPS-C, EPS-N, and EPS-P of both the EPS on Ultisol and Alfisol decreased with increasing solution pH from 3 to 8. Adsorption of EPS-C, EPS-N, and EPS-P of both the EPS on Alfisol significantly increased with increasing ionic strength from 0 to 10 mM, whereas it remained constant, slightly increased, or reduced, when the ionic strength was increased from 10 to 80 mM. The adsorption of EPS-C, EPS-N, and EPS-P on Ultisol slightly increased with increasing ionic strength from 0 to 80 mM. Saturation coverage determined by ATR-FTIR showed that adsorption of whole EPS on Ultisol was higher than that on Alfisol at pH 6 after 60 min. Thus, electrostatic force between EPS and soil colloids played an important role in EPS adsorption. Besides, proteins and phosphate groups in EPS also contributed to EPS adsorption on soil colloids.

Bensulfuron-methyl sorption was studied in Andisol and Ultisol soils in view of their characteristic physical and chemical properties, presenting acidic pH and variable charge. Humic and fulvic acids (HA and FA) and humin (HUM) contributions were established. Sorption was studied by using two synthetic sorbents, an aluminum-silicate with iron oxide coverage and the same sorbent coated with humic acid. Freundlich model described Bensulfuron-methyl behavior in all sorbents (R2 0.969–0.998). Kf for soils (8.3–20.7 μg1−1/n mL1/n g−1) were higher than those reported in the literature. Organic matter, halloysite or kaolinite, and specific surface area contributed to the global process. The highest Kf for HA, FA and HUM were 539.5, 82.9, and 98.7 μg1−1/n mL1/n g−1. Model sorbents described the participation of variable charge materials with high adsorption capacity. The constant capacitance model was used to assess effects of Bensulfuron-methyl adsorption on the distribution of SOH, SOH2+ and SO− sites of sorbents. Organic matter, phyllosilicates, variable charge minerals and organo-mineral complexes contribute to bensulfuron-methyl sorption on volcanic ash-derived soils.

Due to low cost and large abundance, coal continues to be one of the major energy sources for electricity generation in the USA. The dry desulfurization of flue gases during coal combustion produces a by-product that may be potentially useful as a soil amendment. However, the influence of dry flue gas desulfurization (DFGD) by-products on trace element losses with runoff from treated fields has not been well investigated. The objective of this study was to evaluate the effects of land application of a high-Ca, DFGD by-product on trace elements lost in runoff from natural rainfall events. The by-product was applied once on May 18, 2015 at 9 Mg DFGD ha⁻¹ to small plots of a highly weathered Ultisol under managed-grassland land use in northwest Arkansas. Runoff was collected following each runoff-producing precipitation event for 1 year. Seasonal (i.e., summer (May to August), fall (August to November), winter (November to February), and spring (February to May)) runoff, annual runoff, runoff pH, and electrical conductivity did not differ significantly between DFGD treatments. Seasonal flow-weighted mean Ni concentrations and seasonal V loads were significantly greater in runoff when amended versus the unamended control when compared during at least one 3-month season by 44.5 and 86.9% for Ni and V, respectively. Based on the results of this study, it appears that land application of a high-Ca DFGD by-product at rates ≤ 9 Mg ha⁻¹ has minimal effects on trace elements in runoff.

Variable charge soils have low agricultural productivity associated with low pH, low cation exchange capacity (CEC), and low pH buffering capacity (pHBC). As a result of rapid acidification rates, these soils are prone to infertility resulting from Al phytotoxicity and deficiency of P, Ca, Mg, and K, and thus require amendments that can ameliorate soil acidity and enhance soil CEC and pHBC. A 30-day pot experiment was carried out using a clay Ultisol and a sandy Ultisol amended with straw decayed products (SDPs) of peanut, pea, canola, and rice. The results showed that applying SDPs increased the soil CEC, organic matter content, and exchangeable base cations in the two Ultisols. The ameliorative effects of the SDPs were superior for the sandy Ultisol than for the clay Ultisol. The addition of SDPs significantly increased soil pH and pHBC of the two Ultisols, and simultaneously decreased soil exchangeable Al³⁺. Among them, the greatest effect was found in the treatment with pea straw decayed products (PeaSD). The soil pHs of clay Ultisol and sandy Ultisol treated with PeaSD were respectively 5.70 and 7.37 and were 1.26 and 2.63 pH units higher than those of control. Also, applying SDPs increased maize seedling biomass in both soils and the most significant effect was found in the treatment with PeaSD, which were 0.97 (clay Ultisol) and 2.5 (sandy Ultisol) times higher than in the respective controls. The results of this study demonstrated that carefully selected straws for SDP production can effectively improve soil chemical properties, enhanced soil pHBC, and thus promote agricultural sustainability.

Leaching of phosphorus fertilizer from loose-structured subtropical soils is a major course of agricultural water pollution in southeastern USA. Soil amendments play a major role in the phosphorus retention in soil through different mechanisms. In the present study we tested the effect of two soil amendments; biochar and coal fly ash in immobilizing the soluble phosphorus fertilizer added to sandy Ultisol soils from subtropical USA. Column leaching tests were conducted with Ultisol soil added with biochar (from avocado branch cut biomass) and coal fly ash at 5 tons/ha rate, under simulated rainfall, to collect the leachate over five pore volumes. The leachate was analyzed for the phosphate phosphorus content. In the end, the soil columns were carefully extracted, sectioned and analyzed for the total phosphorus, after acid digestion. Results showed 50% and 6% drop of soluble phosphorus leaching loss in biochar and coal fly ash added soil respectively. Soil amendments have shifted the loosely bound phosphorus into the Ca/Mg bound and Al/Fe/Mn bound pools which are not readily water extractable. Addition of biochar and coal fly ash together showed a synergistic interaction effect in reducing the leaching loss of phosphorus which needs further investigation to understand the exact mechanism.

Contamination of soils by nickel (Ni) has become a serious environmental problem throughout the world, and this substance wields dangerous effects on the ecosystem and food chain. A pot experiment was conducted to examine the effect of rice straw (RS), rice straw biochar (BI), and calcite (CC) at 1% and 2% application rates in a Ni-contaminated soil. The objective was to potentially stabilize Ni and reduce its bioavailability to spinach (Spinacia Oleracea L.). Spinach plants were grown in a Ni-contaminated Ultisol (commonly known as a red clay soil). Plant growth parameter results indicated that a BI 2% application rate significantly increased the root and shoots dry biomass increased by 1.7- and 6.3-fold, respectively, while essential nutrients were enhanced in the spinach plant compared to those in the untreated soil (CK). Moreover, adding amendments significantly decreased CaCl₂ extractable Ni by 62.5% 94.1%, and 87.2%, while the toxicity characteristics leaching procedure (TCLP) fell by 26.7%, 47.8%, and 41.7% when using RS, BI, and CC, respectively, at 2% compared to CK. The Ni concentrations in the spinach roots declined by 51.6%, 73.3%, and 68.9%, and in the shoots reduced by 54.1%, 76.7%, and 70.8% for RS, BI, and CC, at a 2% application rate, respectively. Bio-concentration factor (BCF) and translocation factor (TF) dropped significantly by as much as 72.7% and 20%, respectively, for BI 2% application rate. Results of the present study clearly indicated that biochar potential soil amendments for Ni stabilization, thereby reducing its bioavailability in the Ni-contaminated soil. This process enhanced the safety of food to be consumed and mitigated security risks.