ABSTRACT
Nanobiotechnology is a potentially safe and sustainable strategy for both agricultural production and soil remediation, yet the potential of nanomaterials (NMs) application to remediate heavy metal(loid)-contaminated soils is still unclear. A meta-analysis with approximately 6000 observations was conducted to quantify the effects of NMs on safe crop production in soils contaminated with heavy metal(loid) (HM), and a machine learning approach was used to identify the major contributing features. Applying NMs can elevate the crop shoot (18.2 %, 15.4-21.2 %) and grain biomass (30.7 %, 26.9-34.9 %), and decrease the shoot and grain HM concentration by 31.8 % (28.9-34.5 %) and 46.8 % (43.7-49.8 %), respectively. Iron-NMs showed a greater potential to inhibit crop HM uptake compared to other types of NMs. Our result further demonstrates that NMs application substantially reduces the potential health risk of HM in crop grains by human health risk assessment. The NMs-induced reduction in HM accumulation was associated with decreasing HM bioavailability, as well as increased soil pH and organic matter. A random forest model demonstrates that soil pH and total HM concentration are the two significant features affecting shoot HM accumulation. This analysis of the literature highlights the significant potential of NMs application in promoting safe agricultural production in HM-contaminated agricultural lands.
Subject(s)
Crops, Agricultural , Metals, Heavy , Soil Pollutants , Soil , Soil Pollutants/analysis , Metals, Heavy/analysis , Soil/chemistry , Crop Production/methods , Environmental Restoration and Remediation/methods , Nanostructures , Agriculture/methodsABSTRACT
Iron (Fe) oxides are widely recognized to prevent the degradation of organic matter (OM) in environments, thereby promoting the persistence of organic carbon (OC) in soils. Thus, discerning the association mechanisms of Fe oxides and OC interactions is key to effectively influencing the dynamics and extent of organic C cycling in soils. Previous studies have focused on i) quantifying Fe oxide-bound organic carbon (Fe-OC) in individual environments, ii) investigating the distribution and adsorption capacity of Fe-OC, and iii) assessing the redox cycling and transformation of Fe-OC. Furthermore, the widespread application of high-tech instrumentation and methods has greatly contributed to a better understanding of the mechanism of organic mineral assemblages in the past few decades. However, few literature reviews have comprehensively summarized Fe-OC distributions, associations, and characteristics in soil-plant systems. Here, studies investigating the Fe-OC contents among different environments are reviewed. In addition, the mechanisms and processes related to OM transformation dynamics occurring at mineral-organic interfaces are also described. Recent studies have highlighted that diverse interactions occur between Fe oxides and OC, with organic compounds adhering to Fe oxides due to their huge specific surfaces area and active reaction sites. Moreover, we also review methods for understanding Fe-OC interactions at micro-interfaces. Lastly, developmental prospects for understanding coupled Fe-OC geochemical processes in soil environments at molecular- and nano-scales are outlined. The summary suggests that combined advanced techniques and methods should be used in future research to explore micro-interfaces and in situ descriptions of organic mineral assemblages. This review also suggests that future studies need to consider the functional and spatial complexity that is typical of soil/sediment environments where Fe-OC interactions occur.
Subject(s)
Oxides , Soil , Soil/chemistry , Carbon , Minerals/chemistry , Iron , Organic Chemicals/chemistryABSTRACT
Heavy metal (HM) pollution of soils is a globally important ecological and environmental problem. Previous studies have focused on i) tracking pollution sources in HM-contaminated soils, ii) exploring the adsorption capacity and distribution of HMs, and iii) assessing phyto-uptake of HMs and their ecotoxicity. However, few reviews have systematically summarized HM pollution in soil-plant systems over the past decade. Understanding the mechanisms of interaction between HMs and solid soil components is consequently key to effectively controlling and remediating HM pollution. However, the compositions of solid soil phases are diverse, their structures are complex, and their spatial arrangements are heterogeneous, all leading to the formation of soil micro-domains that exhibit different particle sizes and surface properties. The various soil components and their interactions ultimately control the speciation, transformation, and bioavailability of HMs in soils. Over the past few decades, the extensive application of advanced instrumental techniques and methods has greatly expanded our understanding of the behavior of HMs in organic mineral assemblages. In this review, studies investigating the immobilization of HMs by minerals, organic compounds, microorganisms, and their associated complexes are summarized, with a particular emphasis on the interfacial adsorption and immobilization of HMs. In addition, methods for analyzing the speciation and distribution of HMs in aggregates of natural soils with different particle sizes are also discussed. Moreover, we also review the methods for speciating HMs at mineral-organic micro-scale interfaces. Lastly, developmental prospects for HM research at inorganic-organic interfaces are outlined. In future research, the most advanced methods should be used to characterize the interfaces and in situ characteristics of metals and metal complexes. In particular, the roles and contributions of microorganisms in the immobilization of HMs at complex mineral-organic interfaces require significant further investigation.
Subject(s)
Metals, Heavy , Soil Pollutants , Environmental Pollution , Metals, Heavy/analysis , Minerals/chemistry , Soil , Soil Pollutants/analysisABSTRACT
Soil contamination with potentially toxic elements (PTEs) is an increasing environmental problem, posing serious threats to the living organisms. Phytoremediation is a sustainable and highly accepted technology for remediation of PTE-contaminated soils. Alfalfa has been widely adopted for the phytoremediation of PTE-contaminated soils due to its large biomass productivity, high PTE tolerance, and strong capacity to take up PTEs. However, there are still no literature reviews systematically summarized the potential of alfalfa in the phytoremediation. Therefore, we review the available literatures that present its PTE uptake, phytotoxicity, tolerance mechanisms, and aided techniques improving the phytoremediation efficiency. In this review, alfalfa shows high amounts of PTEs accumulation, especially in their root tissue. Meanwhile, the inner mechanisms of PTE tolerance and accumulation in alfalfa are discussed including: (i) the activation of antioxidant enzyme system, (ii) subcellular localization, (iii) production of glutathione, phytochelatins, and proline, and (iv) regulation of gene expression. Indeed, excessive PTE can overcome the defense system, which causes oxidative damage in alfalfa plants, thereby inhibiting growth and physiological processes and weakening the ability of PTE uptake. Till now, several approaches have been developed to improve the tolerance and/or accumulation of PTE in alfalfa plants as follows: (i) selection of PTE tolerant cultivars, (ii) applying plant growth regulators, (iii) addition of chelating agents, fertilizer, and biochar materials, and (iv) inoculation of soil microbes. Finally, we indicate that the selection of PTE-tolerant cultivars along with inoculation of soil microbes may be an efficient and eco-friendly strategy of the soil PTE phytoremediation.
Subject(s)
Soil Pollutants , Soil , Biodegradation, Environmental , Medicago sativa/metabolism , Plants/metabolism , Soil Pollutants/analysisABSTRACT
Zhongjiao No. 9 (Musa spp.), a new Fusarium wilt-resistant banana cultivar, has shown considerable promise in the field. However, the growth, nutrient budgets, and key nutrient mechanisms related to Fusarium wilt resistance have not been explicitly examined. Here, the plant growth, yield, fruit quality, and nutrient budgets of Zhongjiao No. 9 were investigated. The results showed that Zhongjiao No. 9 has a large biomass with a high yield (54.65 t ha-1). The concentrations of N, P, K, Ca, Mg, Mn, B, and Mo were mainly high in the leaves and bunches of mother plants as well as in the leaves and pseudostems of daughter plants, while Cu and Fe were enriched in the roots of both mother plants and daughter plants. Linear discriminant analysis revealed that K, Ca, and Fe were important for plant growth in both the mother plants and daughter plants; S, Zn, and Mn were important for the mother plants, and N, P, and B for were important for the daughter plants. The nutrient uptake ratio of N:P:K:Ca:Mg:S was 1:0.13:3.86:0.68:0.40:0.07. Compared with local cultivars, there was a higher Mg concentration in pseudostems and a higher Mg uptake ratio were observed in Zhongjiao No. 9. Together, our results provide insight into the importance of Mg accumulation in relation to Fusarium wilt resistance, and we provide information on nutrient demands and fertilization application.
ABSTRACT
Plant growth regulators (PGRs) are widely used in agricultural activities and have the potential to improve plant growth and plant tolerance against metal stress. PGR-assisted phytoextraction is now an effective and inexpensive method for enhancing the plant removal of toxic metals from soil. In this study, we conducted experiments to determine the effects of PGR treatments on soil uranium (U) and cadmium (Cd) removal by sunflowers as well as their stress response to U and Cd contamination. We found that the plant growth was inhibited by combined U and Cd stress in sunflowers compared with that of the control; however, the application of exogenous PGR had reduced the combined U and Cd stress by stimulating photosynthesis, decreasing the levels of active oxygen and lipid peroxidation, and enhancing the activity of the antioxidant defence systems. Exogenous PGR also increased the uptake of U and Cd by sunflowers and therefore, improved their U and Cd remediation efficiency. Moreover, indoleacetic acid (IAA) was the most effective PGR at removing U and Cd in the soil; the U and Cd removal efficiency was 484.21% and 238.85% higher in the 500 mg L-1 IAA application compared with that of the control without PGR application, respectively. Furthermore, none of the PGR treatments significantly influenced the available U and Cd contents in soil. Our results, therefore, may provide some detailed understanding on the technologies for the sustainable remediation of U and Cd contaminated soil by the combination of PGR treatments and phytoextraction.
Subject(s)
Biodegradation, Environmental , Cadmium/toxicity , Helianthus/physiology , Plant Growth Regulators/pharmacology , Soil Pollutants/toxicity , Uranium/toxicity , Cadmium/metabolism , Helianthus/growth & development , Indoleacetic Acids , Soil , Soil Pollutants/analysis , Uranium/metabolismABSTRACT
Vanadium(V) is an important component of industrial activities, while it may pose toxic hazards to plants, animals, and humans at high levels. Owing to its various uses in numerous industrial processes, high amount of V is released into the soil environment. Previous literature has focused on the biogeochemistry and ecotoxicity of V in soil-plant system. Consequently, this overview presents its source, fate, phyto-uptake, phyto-toxicity, detoxification, and bioremediation based on available data, especially published from 2015 to 2020. Vanadium occurs as various chemical forms (primarily as V(V) and V(IV)) in the soil environment, and its biogeochemical behaviour is easily influenced by soil conditions including redox potential, soil pH, organic matter, and microorganisms. Vanadium mainly accumulates in plant roots with very limited translocation to shoots. However, plants such as dog's tail grass and green bean are reported to accumulate high levels of V in aboveground tissues. An insight into the processes and mechanisms that allow plants to absorb and translocate V in soil-plant system is also stressed in this overview. In plants, low levels of V have beneficial effects on plant growth and development. Nevertheless, excessive V provokes numerous deleterious effects including reducing seed germination, inhibiting root and shoot growth, depressing photosynthesis, interfering with nutrients uptake, inducing overgeneration of ROS, and leading to lipid peroxidation. Mechanisms related to detoxification strategies like sequestration in root system, compartmentation in vacuoles and cell wall, and antioxidant defence systems to endure V-induced toxicity in plants are discussed as well. The detailed knowledge of bioremediation involved in the cleanup of V-contaminated soils would immensely help understand and improve the remediation process. Furthermore, this overview outlines several research gaps requiring further investigation in order to advance our understanding of the biogeochemical roles of V in soil-plant systems.
Subject(s)
Soil Pollutants , Soil , Biodegradation, Environmental , Plants , Soil Pollutants/analysis , Soil Pollutants/toxicity , Vanadium/toxicityABSTRACT
Knowledge on the distribution of nitrogen (N) pools, processes, and fluxes along hydrological gradients provides a comprehensive perspective to understand the underlying causal mechanisms in intertidal flats, and thus improve predictions and climate adaptation strategies. We used a space-for-time substitution method to quantify N pools, processes, and fluxes along a hydrological gradient. Further, we linked N pools and processes and investigated not only surface but also subsurface sediments. Our results showed a gradual decrease in total N (TN) and mineralization rates (PNmin), but an increase in potential rates of nitrification (PNR) and denitrification (PDNR) under an elevated hydrological gradient, except for TN and PNmin in the subsurface sediment, which accumulated on the interaction zone between the high and middle tidal flats. Most sedimentary ammonium N (NH4+) and nitrate N (NO3-) concentrations were similar; however, NH4+ accumulated on the subsurface of the middle tidal flat. NO3- fluxes (from -0.54 to -0.35 mmol m-2 h-1) were uptake fluxes in the intertidal flats, but NH4+ fluxes (-2.48-3.54 mmol m-2 h-1) changed from uptake to efflux in the seaward direction. Structural equation modeling of the effects of inundation frequency, underground biomass, total carbon (TC), electrical conductivity (EC), and clay proportion on the N processes revealed that these accounted for 67%, 82%, and 17% of the variance of PDNR, PNmin, and PNR, respectively. Inundation frequency, underground biomass, TC, EC, and PNmin effects on N pools accounted for 53%, 69%, and 98% of the variance of NH4+, NO3-, and TN, respectively. This suggests that future sea level rise may decrease N storage due to increase in coupled nitrification-denitrification and decrease in N mineralization, and the NH4+ flux may change from sink to source in intertidal ecosystems.